Ber and other Jujubes monograph.pdf - Crops for the Future
Ber and other Jujubes monograph.pdf - Crops for the Future
Ber and other Jujubes monograph.pdf - Crops for the Future
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Fruits <strong>for</strong> <strong>the</strong> <strong>Future</strong> 2<br />
(Revised edition)<br />
<strong>Ber</strong> <strong>and</strong> <strong>o<strong>the</strong>r</strong> jujubes<br />
Authors<br />
S. Azam-Ali<br />
E. Bonkoungou<br />
C. Bowe<br />
C. deKock<br />
A. Godara<br />
J.T. Williams<br />
Editors<br />
J.T. Williams (chief editor)<br />
R.W. Smith<br />
N. Haq<br />
Z. Dunsiger
First published in 2001 by International Centre <strong>for</strong> Underutilised <strong>Crops</strong>,<br />
University of Southampton, Southampton, SO17 1BJ, UK<br />
2006 Southampton Centre <strong>for</strong> Underutilised <strong>Crops</strong><br />
The text in this document may be reproduced free of charge in any <strong>for</strong>mat or<br />
media without requiring specific permission. This is subject to <strong>the</strong> material not<br />
being used in a derogatory manner or in a misleading context. The source of<br />
<strong>the</strong> material must be acknowledged as [SCUC] copyright <strong>and</strong> <strong>the</strong> title of <strong>the</strong><br />
document must be included when being reproduced as part of an<strong>o<strong>the</strong>r</strong><br />
document or service.<br />
British Library Cataloguing in Publication Data<br />
<strong>Ber</strong><br />
1. tropical fruit trees<br />
i Williams ii Smith iii Haq iv Dunsiger<br />
ISBN 085432 8580<br />
Citation: Azam-Ali, Bonkoungou, Bowe, deKock, Godara, Williams. (2006)<br />
<strong>Ber</strong>. International Centre <strong>for</strong> Underutilised <strong>Crops</strong>, Southampton, UK.<br />
DFID/FRP <strong>and</strong> DISCLAIMERS<br />
This publication is an output from a research project funded by <strong>the</strong> United<br />
Kingdom Department <strong>for</strong> International Development (DFID) <strong>for</strong> <strong>the</strong> benefit of<br />
developing countries. The views expressed are not necessarily those of DFID<br />
[R7187 Forestry Research Programme].<br />
The opinions expressed in this book are those of <strong>the</strong> authors alone <strong>and</strong> do not<br />
imply an acceptance or obligation whatsoever on <strong>the</strong> part of ICUC, SCUC,<br />
ICRAF or IPGRI.
ICUC<br />
The International Centre <strong>for</strong> Underutilised <strong>Crops</strong> (ICUC) is an autonomous, nonprofit,<br />
scientific research <strong>and</strong> training centre. It was established in 1992, based at <strong>the</strong><br />
University of Southampton in <strong>the</strong> UK, but has since moved to <strong>the</strong> headquarters of <strong>the</strong><br />
International Water Management Institute, Sri Lanka. The Centre was established to<br />
address ways to increase <strong>the</strong> use of underutilised crops <strong>for</strong> food, nutrition, medicinal<br />
<strong>and</strong> industrial products. The enhancement of currently underutilised crops is a key to<br />
food security, to <strong>the</strong> conservation of biological diversity <strong>and</strong> to <strong>the</strong> preservation <strong>and</strong><br />
restoration of fragile <strong>and</strong> degraded environments throughout <strong>the</strong> world.<br />
World Agro<strong>for</strong>estry Centre<br />
The World Agro<strong>for</strong>estry Centre (ICRAF), established in Nairobi in 1977, is an<br />
autonomous, non-profit research body supported by <strong>the</strong> Consultative Group on<br />
International Agricultural Research (CGIAR). ICRAF aims to improve human<br />
welfare by alleviating poverty, improving food <strong>and</strong> nutrition security <strong>and</strong> enhancing<br />
environmental resistance in <strong>the</strong> tropics.<br />
IPGRI<br />
The International Plant Genetic Resources Institute (IPGRI) is an international<br />
research institute with a m<strong>and</strong>ate to advance <strong>the</strong> conservation <strong>and</strong> use of genetic<br />
diversity <strong>for</strong> <strong>the</strong> well-being of present <strong>and</strong> future generations. It is also a centre of <strong>the</strong><br />
Consultative Group on International Agricultural Research.<br />
Also available in this series of <strong>monograph</strong>s:<br />
Safou – Dacryodes edulis by J. Kengue (ISBN 0854327649)<br />
Baobab – Adansonia digitata by M. Sidibe <strong>and</strong> J. T. Williams (ISBN 0854327762)<br />
Annona spp. by A. C. de Q. Pinto, M. C. R. Cordeiro, S. R. M. de Andrade, F. R.<br />
Ferreira, H. A. de C. Filgueiras, R. E. Alves <strong>and</strong> D. I. Kinpara (ISBN 0854327851)<br />
Mangosteen – Garcinia mangostana by M. bin Osman <strong>and</strong> Abd. Rahman Milan<br />
(ISBN 0854328173)<br />
Monkey orange – Strychnos cocculoides by C. K. Mwamba (ISBN 0854328416)<br />
Ndjanssang – Ricinodendron heudelotii by Z. Tchoundjeu (ISBN 0854328424)<br />
Sapote species – Pouteria sapota, P. campechiana, P. viridis by C. Azurdia<br />
(ISBN 0854327651)<br />
Forthcoming in this series:<br />
Jackfruit – Artocarpus heterophyllus by N. Haq (ISBN 0854328394)<br />
Tamarind – Tamarindus indica – Revised edition (ISBN 085432 8599)
Contents<br />
Abbreviations..................................................................................................... ii<br />
Preface .............................................................................................................. iii<br />
Chapter 1. Introduction, Taxonomy <strong>and</strong> History ................................................1<br />
1.1 Introduction .....................................................................................1<br />
1.2 The genus Ziziphus ..........................................................................2<br />
1.3 The species of Ziziphus....................................................................3<br />
1.4 The major cultivated species ...........................................................4<br />
1.4.1 Indian jujube...........................................................................4<br />
1.4.2 Chinese jujube ........................................................................5<br />
1.5 The minor cultivated species ...........................................................9<br />
1.5.1 Z. spina-christi (L.) Desf. .......................................................9<br />
1.5.2 Z. lotus (L.) Lam..................................................................10<br />
1.6 Wild species...................................................................................11<br />
1.6.1 Asia.......................................................................................11<br />
1.6.2 Africa....................................................................................12<br />
1.6.3 New World ..........................................................................12<br />
1.7 Vernacular names <strong>for</strong> jujubes ........................................................12<br />
1.8 Historical evidence ........................................................................14<br />
1.8.1 Indian jujube.........................................................................14<br />
1.8.2 Chinese jujube ......................................................................15<br />
Chapter 2. Composition....................................................................................18<br />
2.1 Introduction ...................................................................................18<br />
2.2 Fruit composition...........................................................................18<br />
2.2.1 <strong>Ber</strong> ........................................................................................18<br />
2.2.2 Chinese jujube ......................................................................20<br />
2.3 Ethnopharmaceutical compounds..................................................20<br />
2.3.1 Ascorbic acid, thiamine, riboflavin <strong>and</strong> bioflavonoids.........20<br />
2.3.2 Pectin A ................................................................................21<br />
2.3.3 Alkaloids ..............................................................................21<br />
2.3.4 Glycosides ............................................................................21<br />
2.3.5 Triterpenoic acids .................................................................22<br />
2.3.6 Lipids....................................................................................23<br />
2.4 Nutritional <strong>and</strong> pharmaceutical studies..........................................23<br />
2.4.1 Sweetness inhibitors .............................................................23<br />
2.4.2 Permeability enhancement activity.......................................24<br />
2.4.3 Cytotoxic effect (chem<strong>o<strong>the</strong>r</strong>apy) ..........................................24<br />
2.4.4 Neurological properties ........................................................25<br />
2.4.5 Antifertility/contraception ....................................................26<br />
2.4.6 Hypotensive <strong>and</strong> antinephritic effect....................................26<br />
2.4.7 Cardiovascular activity.........................................................26<br />
2.4.8 Immunostimulant effects ......................................................26
2.4.9 Antifungal activity................................................................26<br />
2.4.10 Antidiabetic ..........................................................................27<br />
2.4.11 Antiallergic...........................................................................27<br />
2.4.12 Antiulcer activity..................................................................27<br />
2.4.13 Antiinflammatory effect .......................................................27<br />
2.4.14 Antispastic effect..................................................................27<br />
2.4.15 Antibacterial .........................................................................27<br />
2.4.16 Antioxidant effects ...............................................................27<br />
2.5 Summary........................................................................................28<br />
Chapter 3. Uses.................................................................................................29<br />
3.1 Introduction ...................................................................................29<br />
3.2 Local uses of fruits ........................................................................29<br />
3.2.1 South, Sou<strong>the</strong>ast <strong>and</strong> East Asia. ...........................................29<br />
3.2.2 Africa....................................................................................29<br />
3.2.3 Southwest Asia .....................................................................30<br />
3.2.4 South America......................................................................30<br />
3.3 Fodder............................................................................................30<br />
3.4 Environmental ...............................................................................31<br />
3.5 Fuelwood .......................................................................................31<br />
3.6 Lac culture.....................................................................................32<br />
3.7 Wood .............................................................................................32<br />
3.8 Bees <strong>and</strong> silkworms.......................................................................32<br />
3.9 Medicinal uses ...............................................................................33<br />
3.9.1 South Asia ............................................................................33<br />
3.9.2 Chinese medicine..................................................................34<br />
3.9.3 O<strong>the</strong>r areas............................................................................34<br />
Chapter 4. Climate <strong>and</strong> Ecology.......................................................................36<br />
4.1 Introduction ...................................................................................36<br />
4.2 Temperature...................................................................................36<br />
4.2.1 <strong>Ber</strong> ........................................................................................36<br />
4.2.2 Chinese jujube ......................................................................37<br />
4.3 Rainfall ..........................................................................................38<br />
4.3.1 <strong>Ber</strong> ........................................................................................38<br />
4.3.2 Chinese jujube .....................................................................38<br />
4.4 Soils...............................................................................................38<br />
4.4.1 <strong>Ber</strong> ........................................................................................38<br />
4.4.2 Chinese jujube ......................................................................39<br />
4.4.3 Stress conditions...................................................................39<br />
Chapter 5. Propagation .....................................................................................40<br />
5.1 Introduction ..................................................................................40<br />
5.2 Seed propagation ...........................................................................40<br />
5.2.1 Seed characteristics ..............................................................40<br />
5.2.2 Seed viability........................................................................41
5.2.3 Seed germination..................................................................42<br />
5.2.4 Seed pretreatments................................................................42<br />
5.2.5 The nursery...........................................................................44<br />
5.3 Vegetative propagation..................................................................48<br />
5.3.1 Rootstocks ............................................................................48<br />
5.3.2 Budding ................................................................................49<br />
5.3.3 Micropropagation .................................................................53<br />
5.3.4 Cuttings <strong>for</strong> Chinese jujube ..................................................54<br />
5.3.5 Grafting ................................................................................55<br />
Chapter 6. Agronomy .......................................................................................56<br />
6.1 Planting..........................................................................................56<br />
6.1.1 Training of plants: ber ..........................................................57<br />
6.1.2 Chinese jujube ......................................................................58<br />
6.2 Water management........................................................................59<br />
6.2.1 Rainfed areas ........................................................................59<br />
6.2.2 Irrigated areas: ber................................................................59<br />
6.2.3 Chinese jujube ......................................................................60<br />
6.2.4 Conservation of moisture......................................................60<br />
6.3 Weeding.........................................................................................60<br />
6.4 Manure <strong>and</strong> fertilisers....................................................................60<br />
6.4.1 Nutrients recommended........................................................61<br />
6.4.2 Foliar feeding........................................................................62<br />
6.4.3 Microbial inoculations..........................................................63<br />
6.5 Pruning ..........................................................................................63<br />
6.5.1 Pruning intensity...................................................................63<br />
6.5.2 Pruning in Chinese jujube.....................................................65<br />
6.5.3 Pruning time .........................................................................65<br />
6.6 Pests...............................................................................................66<br />
6.6.1 Fruitfly..................................................................................66<br />
6.6.2 Fruit borer.............................................................................67<br />
6.6.3 Bark eating caterpillar ..........................................................68<br />
6.6.4 Hairy caterpillars ..................................................................68<br />
6.6.5 Chafer beetle (ber beetle or leaf chafer) ...............................69<br />
6.6.6 Lac insect..............................................................................70<br />
6.6.7 O<strong>the</strong>r insect pests..................................................................70<br />
6.6.8 Mites.....................................................................................70<br />
6.7 Diseases .........................................................................................71<br />
6.7.1 Powdery mildew...................................................................71<br />
6.7.2 Alternaria leaf spot...............................................................72<br />
6.7.3 Black leaf spot ......................................................................73<br />
6.7.4 Cercospora leaf spot.............................................................74<br />
6.7.5 Cladosporium leaf spot.........................................................74<br />
6.7.6 Rust.......................................................................................75<br />
6.7.7 Witches’ broom ....................................................................75<br />
6.7.8 Fruit rot.................................................................................75
6.7.9 Minor foliar pathogens .........................................................77<br />
6.8 Cropping systems ..........................................................................77<br />
Chapter 7. Breeding..........................................................................................79<br />
7.1 Introduction ...................................................................................79<br />
7.2 Breeding objectives .......................................................................80<br />
7.3 Constraints/ bottlenecks in breeding..............................................81<br />
7.4 Breeding methods..........................................................................81<br />
7.4.1 Selection ...............................................................................81<br />
7.4.2 Hybridisation ........................................................................83<br />
7.4.3 Mutation ...............................................................................84<br />
7.4.4 Polyploidy ............................................................................86<br />
7.4.5 Biotechnological methods ....................................................87<br />
7.4.6 Current situation ...................................................................89<br />
Chapter 8. Genetic Resources...........................................................................91<br />
8.1 The Ziziphus genepool...................................................................91<br />
8.1.1 Chromosome numbers..........................................................91<br />
8.1.2 Hybridisation ........................................................................92<br />
8.2 Cultivars ........................................................................................93<br />
8.2.1 Morphological variability <strong>and</strong> characterisation ....................93<br />
8.2.2 Reproductive variability .......................................................95<br />
8.2.3 Yield .....................................................................................99<br />
8.2.4 Chemical variability ...........................................................100<br />
8.2.5 Genetic variability ..............................................................102<br />
8.2.6 Distribution of important traits ...........................................106<br />
8.3 Collections ...................................................................................108<br />
8.3.1 Genetic erosion...................................................................108<br />
8.3.2 Existing collections ............................................................108<br />
8.3.4 Conservation methodologies ..............................................111<br />
Chapter 9. Harvesting, post-harvest h<strong>and</strong>ling <strong>and</strong> processing ........................113<br />
9.1 Introduction .................................................................................113<br />
9.2 <strong>Ber</strong> ...............................................................................................113<br />
9.2.1 Harvesting ..........................................................................113<br />
9.2.2 Post harvest h<strong>and</strong>ling..........................................................120<br />
9.2.3 Processing...........................................................................126<br />
9.3 O<strong>the</strong>r jujubes ...............................................................................139<br />
9.3.1 Ripening .............................................................................139<br />
9.3.2 Treatments ..........................................................................140<br />
9.3.3 Storage................................................................................140<br />
9.3.4 Processing of Chinese jujube..............................................140<br />
9.3.5 O<strong>the</strong>r Chinese jujube products ...........................................153<br />
Chapter 10. Marketing....................................................................................153<br />
10.1 Introduction .................................................................................154
10.2 <strong>Ber</strong> ...............................................................................................154<br />
10.3 Chinese jujube .............................................................................159<br />
10.4 Market prospects..........................................................................159<br />
Chapter 11. Current situation <strong>and</strong> research needs...........................................160<br />
11.1 Summary of <strong>the</strong> current situation.................................................160<br />
11.2 Need <strong>for</strong> in<strong>for</strong>mation dissemination ............................................161<br />
11.3 Research needs ............................................................................162<br />
11.3.1 Underst<strong>and</strong>ing <strong>the</strong> genetic variation ...................................162<br />
11.3.2 Genetic improvement .........................................................163<br />
11.3.3 Propagation.........................................................................165<br />
11.3.4 Pruning/cropping systems...................................................165<br />
11.3.5 Post-harvest studies ............................................................166<br />
11.3.6 Marketing ...........................................................................166<br />
11.3.7 O<strong>the</strong>r relevant development issues .....................................166<br />
References ......................................................................................................167<br />
Appendix I Insect <strong>and</strong> mite pests of ber (Pareek 2001, updated)....................258<br />
Appendix II Ziziphus cultivars........................................................................261<br />
Appendix III Research organisations working on jujubes ..............................268<br />
Appendix IV List of jujube specialists............................................................273<br />
Appendix V Seed suppliers directory .............................................................275<br />
Glossary..........................................................................................................278<br />
Index...............................................................................................................285
Tables<br />
Table 1.1 Vernacular names <strong>for</strong> jujubes<br />
Table 2.1 Nutritional constituents in fruit pulp of 4 ber cultivars<br />
Table 4.1 Ecological background of three Ziziphus species<br />
Table 6.1 Planting distance of ber<br />
Table 6.2 Nutrient practices in ber orchards in India<br />
Table 7.1 Ideotypes of ber<br />
Table 8.1 Classification of germplasm of ber in different clusters<br />
Table 8.2 Important traits in ber<br />
Table 8.3 Traits identified in ber cultivars<br />
Table 8.4 Indian Institutions holding ber germplasm collections<br />
Table 8.5 Species used <strong>for</strong> rootstocks <strong>for</strong> Indian jujube<br />
Table 8.6 Exploitable attributes of wild species in ber improvement<br />
Table 9.1 Maturity indices <strong>for</strong> cultivars of ber<br />
Table 9.2 The effects of spraying E<strong>the</strong>phon on <strong>the</strong> number of harvests<br />
of ber fruit<br />
Table 9.3 Grading criteria <strong>for</strong> ber<br />
Table 9.4 Typical changes in quality characteristics of ber fruit during<br />
storage at ambient temperature<br />
Table 9.5 Optimum blanching times <strong>for</strong> ber cultivars.<br />
Table 10.1 Percent price spread of ber in marketing through different<br />
channels in Chomu market (India)<br />
Table 10.2 Components of cost in marketing of ber through different<br />
channels at Chomu market in India<br />
13<br />
19<br />
36<br />
56<br />
61<br />
79<br />
106<br />
106<br />
107<br />
109<br />
110<br />
111<br />
114<br />
117<br />
121<br />
123<br />
127<br />
156<br />
157<br />
Figures<br />
Figure 1.1 Branch <strong>and</strong> leaf arrangement in ber showing <strong>the</strong> unequal<br />
spines<br />
Figure 1.2 Flower <strong>and</strong> fruit of ber showing <strong>the</strong> pistil, stamens <strong>and</strong> seed<br />
Figure 5.1 The budwood<br />
Figure 5.2 Methods of budding<br />
Figure 6.1 Training ber - after planting or in situ budding<br />
Figure 6.2 Training in ber<br />
7<br />
8<br />
50<br />
52<br />
57<br />
58
Plates<br />
Plate 1. 30 day old rootstock seedling in polytube.<br />
Plate 2. 100 day old rootstock seedling in polytube ready <strong>for</strong><br />
transplanting or budding<br />
Plate 3. Scion buds successfully sprouted<br />
Plate 4. Rootstock prepared <strong>for</strong> patch or shield budding<br />
Plate 5. Patch <strong>and</strong> shield buds inserted on <strong>the</strong> rootstocks<br />
Plate 6. Scion buds tied after insertion<br />
Plate 7. Fruitfly infested ber fruits<br />
Plate 8. Twigs infested by lac insects<br />
Plate 9. Powdery mildew infestation on young fruits <strong>and</strong> leaves<br />
Plate 10. Alternaria leaf spot<br />
Plate 11. Isariopsis leaf spot<br />
Plate 12. Rust on leaves<br />
Plate 13. Alternaria fruit spot<br />
Plate 14. Chinese date <strong>and</strong> peanut intercropping<br />
Plate 15. Morphological variability of leaves in Z. mauritiana<br />
Plates 16. & 17. Flowering <strong>and</strong> fruit set in Z. mauritiana<br />
Plate 18. cv. Ponda<br />
Plate 19. cv. Illaoichi<br />
Plate 20. cv. Umran<br />
Plate 21. cv. Kaithli<br />
Plate 22. cv. Banarsi Kadaka<br />
Plate 23. cv. Seb<br />
Plate 24. cv. Gola<br />
Plate 25. cv. Katha Phal<br />
Plate 26. Morphological variability of fruits in Z. mauritiana<br />
Plate 27. Morphological variability of stones in Z. mauritiana<br />
141<br />
141<br />
141<br />
142<br />
142<br />
142<br />
143<br />
143<br />
144<br />
144<br />
145<br />
145<br />
145<br />
146<br />
146<br />
147<br />
148<br />
148<br />
149<br />
149<br />
150<br />
150<br />
150<br />
150<br />
152<br />
152
Abbreviations<br />
ABA -<br />
AMP -<br />
BA -<br />
CIAH -<br />
CAN -<br />
DFID -<br />
dSM -<br />
ESP -<br />
FAO -<br />
GA -<br />
GDH -<br />
GOT -<br />
IAA -<br />
IBA -<br />
ICRAF -<br />
ICUC -<br />
IPGRI -<br />
IPM -<br />
IU -<br />
MPa -<br />
MS medium -<br />
NAA -<br />
NOXA -<br />
NRCAH -<br />
RH -<br />
SALWA -<br />
SAR -<br />
TBZ -<br />
TIBA -<br />
TMV -<br />
TSS -<br />
WHO -<br />
VAM -<br />
Abscissic Acid<br />
Adenosine monophosphate<br />
Benzyladenine<br />
Central Institute <strong>for</strong> Arid Horticulture<br />
Calcium ammonium nitrate (fertiliser)<br />
Department <strong>for</strong> International Development (UK)<br />
Decisiemen (unit measurement <strong>for</strong> soil salinity).<br />
Exchangeable Sodium Percentage<br />
Food <strong>and</strong> Agriculture Organization of <strong>the</strong> United Nations<br />
Gibberellic Acid<br />
Glutamine dehydrogenase<br />
Glutamate Oxalacetate Transaminase<br />
Indole Acetic Acid<br />
Indole Butyric Acid<br />
World Agro<strong>for</strong>estry Centre (<strong>for</strong>merly International Centre <strong>for</strong><br />
Research in Agro<strong>for</strong>estry)<br />
International Centre <strong>for</strong> Underutilised <strong>Crops</strong><br />
International Plant Genetic Resources Institute<br />
Integrated Pest Management<br />
International Unit<br />
Megapascals (unit of measurement <strong>for</strong> osmotic potential)<br />
Murashige <strong>and</strong> Skoog medium<br />
Napthylacetic Acid<br />
Napthoxyacetic Acid<br />
National Research Centre <strong>for</strong> Arid Horticulture (India)<br />
Relative Humidity<br />
Semi Arid Lowl<strong>and</strong>s of West Africa project of ICRAF<br />
Sodium Adsorption Ratio<br />
Thiabendazole<br />
2,3,5-tri-iodobenzoic acid<br />
Tobacco Mosaic Virus<br />
Total Soluble Solids<br />
World Health Organization<br />
Vesicular Arbuscular Mycorrhizal fungi<br />
ii
Preface<br />
<strong>Jujubes</strong> are considered to be minor fruits <strong>and</strong>, from a research <strong>and</strong> development<br />
point of view, have not received any major emphasis from governments.<br />
However <strong>the</strong> fruits are an integral part of <strong>the</strong> culture <strong>and</strong> way of life of millions<br />
of diverse Asian peoples <strong>and</strong> have also become so <strong>for</strong> large regions of Africa<br />
after <strong>the</strong> major cultivated species were introduced.<br />
There has been sustained recognition from scientists, particularly those in<br />
national agricultural programmes, that <strong>the</strong>se fruits can be exploited much more<br />
widely due to <strong>the</strong>ir value in human nutrition <strong>and</strong> <strong>the</strong> added benefits to rural<br />
people of <strong>o<strong>the</strong>r</strong> products from a multipurpose tree. Additionally <strong>the</strong> trees are<br />
hardy <strong>and</strong> can be cultivated in a very wide range of climatic <strong>and</strong> agroecological<br />
zones <strong>the</strong>reby making <strong>the</strong>m of great value in agricultural <strong>and</strong> human<br />
development in areas where intensive agriculture is not currently feasible.<br />
When <strong>the</strong> International Centre <strong>for</strong> Underutilised <strong>Crops</strong> (ICUC) initiated a<br />
project on Fruits <strong>for</strong> <strong>the</strong> <strong>Future</strong> one of <strong>the</strong> first <strong>monograph</strong>s to be produced<br />
focused on Indian jujube or ber (Ziziphus mauritiana). This was authored by Dr<br />
O.P. Pareek <strong>and</strong> issued in 2001. ICUC was gratified to note <strong>the</strong> great dem<strong>and</strong><br />
<strong>for</strong> this <strong>monograph</strong> (over 1200 copies in 5 years) <strong>and</strong> also to note that research<br />
was accelerating in <strong>the</strong> period since it was issued. Continual requests <strong>for</strong> more<br />
in<strong>for</strong>mation, especially from Africa, led ICUC to decide that a revised<br />
<strong>monograph</strong> was needed. This book is <strong>the</strong> result of that decision; it draws, as<br />
would be expected, heavily on <strong>the</strong> initial work of Dr Pareek, to whom ICUC<br />
again expresses its thanks.<br />
This is a multiauthored publication <strong>and</strong> we would like to thank <strong>the</strong> authors <strong>for</strong><br />
<strong>the</strong>ir contribution. The preparation <strong>and</strong> publication of <strong>the</strong> original <strong>monograph</strong><br />
<strong>and</strong> <strong>the</strong> present one has been funded by <strong>the</strong> Department <strong>for</strong> International<br />
Development (DFID), UK. The goal of <strong>the</strong> Fruits <strong>for</strong> <strong>the</strong> <strong>Future</strong> Project is to<br />
provide a useful compendium on a priority underutilised fruit to researchers,<br />
teachers, students, extensionists, growers, traders <strong>and</strong> policy makers in <strong>the</strong> hope<br />
that it could encourage enhanced production, processing <strong>and</strong> marketing of<br />
jujubes.<br />
ICUC expresses its thanks to DFID <strong>and</strong> to <strong>the</strong> numerous national scientists <strong>and</strong><br />
<strong>o<strong>the</strong>r</strong>s who have contributed in one way or an<strong>o<strong>the</strong>r</strong> to <strong>the</strong> two <strong>monograph</strong>s.<br />
Editors 2006<br />
iii
Chapter 1. Introduction, Taxonomy <strong>and</strong><br />
History<br />
1.1 Introduction<br />
J.T. Williams<br />
<strong>Jujubes</strong> are species of <strong>the</strong> genus Ziziphus Tourn. ex L. Ziziphus belongs to <strong>the</strong><br />
family Rhamnaceae named <strong>for</strong> <strong>the</strong> genus Rhamnus. Along with genera <strong>o<strong>the</strong>r</strong><br />
than Ziziphus, Rhamnus does not include many economic species except <strong>for</strong><br />
some wild species with edible fruits or of interest <strong>for</strong> medicinal products or<br />
dyestuffs. The Rhamnaceae have fruits which are drupes or are dry <strong>and</strong> are<br />
closely related to an<strong>o<strong>the</strong>r</strong> family, Vitaceae, which includes major economic<br />
species whose fruits are berries.<br />
The name Ziziphus is related to an Arabic word used along <strong>the</strong> North African<br />
coast, zizoufo used <strong>for</strong> Z. lotus (L.) Desf., but also related to <strong>the</strong> ancient Persian<br />
words zizfum or zizafun; <strong>and</strong> ancient Greeks used <strong>the</strong> word ziziphon <strong>for</strong> <strong>the</strong><br />
jujube.<br />
There are two major domesticated jujubes, Z. mauritiana Lam. <strong>the</strong> Indian<br />
jujube or ber, <strong>and</strong> Z. jujuba Mill. <strong>the</strong> Chinese or common jujube. These two<br />
species have been cultivated over vast areas of <strong>the</strong> Old World <strong>and</strong> a limited<br />
number of <strong>o<strong>the</strong>r</strong>s have been, <strong>and</strong> are, cultivated on a more localised scale.<br />
However all jujubes remain relatively minor crops although dem<strong>and</strong> <strong>for</strong><br />
production remains steady in many parts where <strong>the</strong>y were originally<br />
domesticated.<br />
Interest in exp<strong>and</strong>ing <strong>the</strong> use of <strong>the</strong>se underutilised crops has been sporadic<br />
over <strong>the</strong> decades particularly in relation to rural development objectives. In<br />
1980 <strong>the</strong> National Academy of Sciences noted <strong>the</strong> two major jujubes (along<br />
with Z. nummularia (Burm.) Wight & Arn. <strong>and</strong> Z. spina-christi (L.) Desf.) are<br />
useful species <strong>for</strong> firewood in arid <strong>and</strong> semi-arid zones (NAS, 1980, also see<br />
Adams et al,. 1978). At about <strong>the</strong> same time an assessment of species <strong>for</strong><br />
exp<strong>and</strong>ed use in <strong>the</strong> Sahelian regions noted <strong>the</strong> multipurpose value of jujube<br />
species including food, honey production, <strong>for</strong>age <strong>and</strong> environmental protection<br />
(von Maydell, 1986, originally in German 1981), although this assessment did<br />
not accord to <strong>the</strong>se species any value <strong>for</strong> firewood or charcoal. In <strong>the</strong> 1990s <strong>the</strong><br />
International Centre <strong>for</strong> Underutilised <strong>Crops</strong> (ICUC), following a number of<br />
consultations with national programmes in Africa <strong>and</strong> Asia, highlighted Z.<br />
mauritiana as a priority species <strong>for</strong> enhanced research attention.<br />
India had already included Z. mauritiana in its national programme on<br />
underutilised crops, <strong>and</strong> ICUC was <strong>for</strong>tunate in having a scientist associated<br />
1
with that programme write a specific <strong>monograph</strong> (Pareek, 2001). Similarly<br />
<strong>o<strong>the</strong>r</strong> national programmes were recognizing that jujube species were<br />
underutilised <strong>and</strong> could be given priority e.g. Chinese jujube in Azerbaijan<br />
(Tagiev, 1992). In <strong>the</strong> New World <strong>the</strong>re are some indigenous species of jujube<br />
but none are considered economic. Chinese jujube has been introduced <strong>and</strong><br />
grown under plantation conditions in Cali<strong>for</strong>nia <strong>and</strong> Florida. The USDA has<br />
imported germplasm of ber <strong>and</strong> a small amount is cultivated in Florida.<br />
In general, fruits of jujubes are used in areas where <strong>the</strong>ir products are fresh or<br />
dried fruits (hence <strong>the</strong> names Chinese date <strong>and</strong> Indian date) <strong>for</strong> later use. A<br />
range of processed products also exist wherever <strong>the</strong> species are grown.<br />
1.2 The genus Ziziphus<br />
Ziziphus P. Miller, Abbrev. Gard. Dict. 1754<br />
Erect trees or small to large shrubs or semi-sc<strong>and</strong>ent shrubs or climbers; when<br />
trees usually with a deep radicle, well developed; species may be spiny or not<br />
but more commonly are so <strong>and</strong> species may be glabrous or relatively hairy. The<br />
same species may occasionally be found with specimens which are trees <strong>and</strong><br />
<strong>o<strong>the</strong>r</strong>s which are shrubs.<br />
Leaves are alternate or rarely subopposite; <strong>the</strong>y are simple <strong>and</strong> coriaceous or<br />
membranous, acuminate, too<strong>the</strong>d or not, <strong>and</strong> 3-5-nerved from <strong>the</strong> base; <strong>the</strong> leaf<br />
base is ei<strong>the</strong>r asymmetrical, slightly asymmetrical or symmetrical. Leaves are<br />
petiolated with stipules often spinous <strong>and</strong> branchlets often zigzag.<br />
Flowers are 5-merous, actinomorphic <strong>and</strong> hermaphrodite. Flowers are borne<br />
sometimes solitary or 2-3 toge<strong>the</strong>r in axillary cymes or in umbels or racemes<br />
arranged in terminal panicles or thyrses. Inflorescences may be pedunculate or<br />
sessile.<br />
Calyx with triangular acute lobes up to 2 mm long, dentate; calyx valvate,<br />
keeled on <strong>the</strong> inside <strong>and</strong> <strong>the</strong> tube obconical. Petals also about 2 mm long,<br />
unguiculate at <strong>the</strong> base, deflexed with <strong>the</strong> exp<strong>and</strong>ed parts about 1.5 mm wide.<br />
The petals clasp <strong>the</strong> stamens or <strong>the</strong> filaments. Occasionally petals are absent.<br />
Stamens 5 at least, partly adnate to <strong>the</strong> petal bases <strong>and</strong> filaments are inserted<br />
under <strong>the</strong> edge of <strong>the</strong> disk; stamens usually exceed petals. Ovary is superior or<br />
subinferior <strong>and</strong> sunk into <strong>the</strong> disk but not coherent with it <strong>and</strong> adnate to <strong>the</strong><br />
receptacle, <strong>the</strong> latter being obconical. The disk has 5 or 10 lobes, is rarely<br />
entire <strong>and</strong> its margin is free. The ovary is 2-4 celled with 2-4 styles (usually 2)<br />
which are distinct but can be somewhat connate. When 2-celled usually only 1<br />
produces a seed.<br />
2
Fruits are subglobose, ovoid or oblong, usually drupes. They are 1-4 celled <strong>and</strong><br />
1-4 seeded but drupes mostly contain 1 seed. The flesh of <strong>the</strong> drupe is usually<br />
juicy pulp but may rarely be relatively dry. Young fruits may be pilose or not.<br />
Seeds contain large embryos with endosperm sparse or absent. Fruiting<br />
branchlets may or may not be deciduous.<br />
Most earlier divisions of <strong>the</strong> genus were based on characteristics of <strong>the</strong><br />
inflorescences (e.g. Hooker, 1875; Br<strong>and</strong>is, 1906; Sussenguth, 1953). Liu <strong>and</strong><br />
Cheng (1995) considered details of inflorescence types unstable <strong>and</strong> suggested<br />
that <strong>the</strong> species are grouped into two Sections, one fur<strong>the</strong>r divided into two<br />
Series:<br />
1. Ziziphus - Occurring in temperate zones. Plants glabrous <strong>and</strong> with<br />
deciduous fruiting branchlets.<br />
2. Perdurans - M. J. Liu <strong>and</strong> C. Y. Cheng - Occurring in subtropical <strong>and</strong><br />
tropical zones. Plants pilose <strong>and</strong> without deciduous fruiting branchlets.<br />
2.1 Series Cymosiflorae - Occurring widely in subtropical <strong>and</strong><br />
tropical zones. Flowers in axillary cymes. Ovary <strong>and</strong> fruit glabrous<br />
with thick, hard endocarp.<br />
2.2 Series Thyrsiflorae - Occurring in South <strong>and</strong> Sou<strong>the</strong>ast Asia.<br />
Flowers in terminal or axillary thyrses. Ovary <strong>and</strong> young fruit pilose<br />
with very thin endocarp.<br />
The Indian jujube belongs to Section Perdurans Series Cymosiflorae <strong>and</strong> <strong>the</strong><br />
Chinese jujube belongs to Section Ziziphus. The more minor cultivated species<br />
can also be classified in Series Cymosiflorae.<br />
1.3 The species of Ziziphus<br />
There is a consensus that <strong>the</strong> genus contains about 86 species (Evreinoff, 1964;<br />
Johnston, 1972) but <strong>o<strong>the</strong>r</strong>s suggest <strong>the</strong>re could be up to 135 (Bhansali, 1975)<br />
<strong>and</strong> Liu <strong>and</strong> Cheng, (1995) suggested <strong>the</strong>re could be up to 170. Much depends<br />
on <strong>the</strong> taxonomist’s view of a species; however in <strong>the</strong> past <strong>the</strong>re have been 271<br />
names given, many of <strong>the</strong>m reduced to synonymy.<br />
One problem in underst<strong>and</strong>ing a somewhat complex taxonomy has been that<br />
<strong>the</strong> same specific name has been used by different authors <strong>for</strong> different species.<br />
Sometimes in published papers it is difficult always to be sure which species is<br />
meant, especially when an authority <strong>for</strong> <strong>the</strong> name is not given or when <strong>the</strong>re is<br />
no voucher specimen to ensure <strong>the</strong> right identity. The Indian jujube (Z.<br />
mauritiana Lam.) has had <strong>the</strong> specific name of jujuba applied as Z. jujuba (L.)<br />
Lam. <strong>and</strong> Z. jujuba (L.) Gaertn. <strong>and</strong> named intraspecific taxa of <strong>the</strong> latter refer<br />
to an<strong>o<strong>the</strong>r</strong> species Z. abyssinica A. Rich, which in turn had been called Z.<br />
jujuba Hemsl. There are numerous examples such as this one among <strong>the</strong><br />
synonymy especially with specific names such as rotundifolia or nummularia.<br />
3
Less serious, but also a constraint, is that accounts <strong>and</strong> naming of species,<br />
although <strong>the</strong>y may be based on very wide geographical areas, have not<br />
included inter-regional comparisons. For instance, Johnston (1972) considered<br />
possible affinities between Z. lotus of Mauritania <strong>and</strong> <strong>the</strong> Sahara, <strong>and</strong> Z. hamer<br />
of East Africa <strong>and</strong> Z. leucodermis (Baki) O. Schwartz of Arabia but concluded<br />
that a thorough field study is desirable.<br />
Lastly, in underst<strong>and</strong>ing <strong>the</strong> complexity of <strong>the</strong> taxonomy of Ziziphus species,<br />
hybridisation can be a problem. Confusing species boundaries <strong>and</strong> names have<br />
been given to some stabilised segregates. This will be discussed in Chapter 8.<br />
1.4 The major cultivated species<br />
1.4.1 Indian jujube<br />
Ziziphus mauritiana Lam.<br />
Synonyms<br />
Z. jujuba (L.) Lam.<br />
Z. jujuba (L.) Gaertn. (including var. stenocarpa Kuntze <strong>and</strong> <strong>for</strong>ma<br />
aequilatrifolia Engl.)<br />
Z. tomentosa Poir.<br />
Z. rotundata D.C.<br />
Z. aucheri Boiss.<br />
Z. insularis Smith<br />
Z. sororia Roem. <strong>and</strong> Schult.<br />
Z. orthocantha D.C.<br />
The species has a wide range of morphologies from shrubs to small or mediumsized<br />
trees which might be erect, semi-erect or spreading. Height can vary from<br />
3-4 to 10-16 m or more although trees of 20 m are rare. Trees are semideciduous<br />
<strong>and</strong> much branched. The bark has deep longitudinal furrows <strong>and</strong> is<br />
greyish brown or reddish in colour. Usually <strong>the</strong> shrub or tree is spinous, but<br />
occasionally unarmed.<br />
Branchlets are densely white pubescent, especially when young <strong>and</strong> tend to be<br />
zig-zag. Branches erect <strong>and</strong> spreading, becoming flexuous <strong>and</strong> dull browngrey.<br />
Fruiting branches are not deciduous.<br />
Leaf laminae are elliptic to ovate or nearly orbicular, (1.3-)3-8(-12) cm long<br />
<strong>and</strong> (0.4-)1.5-5(-6.5) cm at <strong>the</strong> widest point. The apex is rounded, obtuse or<br />
subacute to emarginated, <strong>the</strong> base rounded, sometimes cuneate, mostly<br />
symmetrical or nearly so. Margins are minutely serrulate. There are 3 marked<br />
nerves almost to <strong>the</strong> apex, <strong>the</strong> nerves being depressed in <strong>the</strong> upper, light or dark<br />
green, glabrous surface. Lower surface is whitish due to persistent dense hairs<br />
but may be buff coloured. Occasionally <strong>the</strong> lower surface is glabrous.<br />
4
Leaves are petiolate 1.1-5.8 mm long <strong>and</strong> stipules are mostly spines, in each<br />
pair one hooked <strong>and</strong> one straight, or both hooked, or more rarely nei<strong>the</strong>r<br />
developed into a spine.<br />
Flowers have sepals which are dorsally tomentose, a disk about 3 mm in<br />
diameter <strong>and</strong> a 2-celled ovary, immersed in <strong>the</strong> disk. Styles are 2, 1 mm long<br />
<strong>and</strong> connate <strong>for</strong> half <strong>the</strong>ir length. Flowers tend to have an acrid smell.<br />
Flowers are borne in cymes or small axillary clusters. Cymes can be sessile or<br />
shortly pedunculate, peduncles 1-4 mm tomentose. Pedicels are also tomentose<br />
<strong>and</strong> are 2-4 mm at flowering <strong>and</strong> 3-6 mm at fruiting.<br />
Fruit is a glabrous globose or oval edible drupe varying greatly in size from<br />
(1-) 1.5 (-2) cm diameter but some oval varieties can reach 5 x 3 cm. The pulp<br />
is acidic <strong>and</strong> sweet, <strong>the</strong> fruit greenish, yellow or sometimes reddish.<br />
The species is distributed throughout <strong>the</strong> warm subtropics <strong>and</strong> tropics of South<br />
Asia. In cultivation it has spread south-eastwards through Malesia <strong>and</strong><br />
eastwards through IndoChina <strong>and</strong> sou<strong>the</strong>rn China. It is widespread in Africa<br />
<strong>and</strong> sou<strong>the</strong>rn Arabia, where it was probably first cultivated; however in Africa<br />
it has naturalised <strong>and</strong> so-called ‘wild’ types are to be found, especially shrubby<br />
ra<strong>the</strong>r than tree <strong>for</strong>ms. It adapts to warm to hot tropical climates with low to<br />
relatively high rainfall, tolerating poor soils.<br />
The intraspecific taxa described are not very meaningful in view of this<br />
tendency to naturalise <strong>and</strong> produce wild heterogeneous populations. Several<br />
varietal names have been given to wild morphotypes. One variety, Z.<br />
mauritiana var. orthocantha (D.C.) A. Cher. is found south of <strong>the</strong> western<br />
Sahara <strong>and</strong> in Mauritania. It produces a dry pulp <strong>and</strong> is probably valid in view<br />
of its specific utilisation by local people.<br />
1.4.2 Chinese jujube<br />
Ziziphus jujuba Mill.<br />
Synonyms<br />
Z. sativa Gaertn.<br />
Z. vulgaris Lam.<br />
Z. flexuosa Wall.<br />
Z. nitida Roxb.<br />
Z. sinensis Lam.<br />
Z. zizyphus (L.) Karst.<br />
Z. mairei Dode<br />
Z. officinarum Med.<br />
Z. chinensis D.C.<br />
Z. chinensis Watt<br />
5
Shrubs or small trees up to 8-10 m high with rigid spreading boughs <strong>and</strong> stiff<br />
branches; an appearance often producing a gnarled shape. Tree <strong>for</strong>ms tend to<br />
have a small canopy extending 3.5-4.5 m. Trunks may be short or long<br />
depending on genotype. Branches are armed with paired spikes, one of each<br />
pair larger than <strong>the</strong> <strong>o<strong>the</strong>r</strong> <strong>and</strong> straight, <strong>the</strong> shorter one recurved. Older parts of<br />
older trees can lose <strong>the</strong>ir spines. Branchlets are flexuous, green <strong>and</strong> glabrous<br />
when young. Fruiting branchlets are deciduous.<br />
Leaves are (2-) 2.5-5 (-5.5) cm long oblong, obtuse, glabrous (rarely tomentose<br />
beneath), gl<strong>and</strong>ular, crenate-serrate, 3-nerved. Petioles are 2.5-7.5 cm long.<br />
Stipules <strong>for</strong>m <strong>the</strong> spines.<br />
Flowers are few in a small axillary cluster or cyme which is larger than its<br />
peduncle. Flowers have a disk obscurely lobed. Styles are 2, connate <strong>for</strong> half<br />
<strong>the</strong>ir length.<br />
Fruit is an ovoid-oblong edible drupe 1.5-2.3 cm long, dark reddish brown to<br />
black, each being short stalked <strong>and</strong> may be pendulous. Pulp sour to sweet.<br />
Chinese jujube is native to temperate Asia, particularly China <strong>and</strong> neighbouring<br />
areas of Mongolia <strong>and</strong> <strong>the</strong> Central Asian Republics. In cultivation it spread<br />
westwards to <strong>the</strong> Mediterranean, throughout <strong>the</strong> Near East <strong>and</strong> SW Asia <strong>and</strong><br />
spread eastwards in cultivation to Korea <strong>and</strong> Japan. Like Z. mauritiana this<br />
species also naturalises in many Asian countries <strong>and</strong> ‘wild’ populations are to<br />
be found which are derivatives from cultivation. It is mostly cultivated in<br />
China, India, Central Asia <strong>and</strong> southwest Asia.<br />
Z. jujuba var. spinosa Hu ex H. F. Chow is typified by possession of small sour<br />
fruits <strong>and</strong> is usually a spiny shrub or small tree (Wang <strong>and</strong> Sun, 1986). Z.<br />
jujuba var. inermis has unarmed branches <strong>and</strong> styles not connate (Br<strong>and</strong>is,<br />
1874).<br />
Chinese jujube is adapted to subtropical <strong>and</strong> warm temperate areas. It prefers a<br />
relatively dry climate during <strong>the</strong> growing season but cool during its dormancy.<br />
It can tolerate lower temperatures than Indian jujube <strong>and</strong> can survive -10°C.<br />
There should be no confusion between <strong>the</strong> Chinese jujube <strong>and</strong> <strong>the</strong> description<br />
of Z. jujuba (L.) Gaertn. var. hysudrica Edgew which relates to reputed hybrids<br />
of Z. mauritiana <strong>and</strong> Z. spina-christi.<br />
6
Figure 1.1 Branch <strong>and</strong> leaf arrangement in ber showing <strong>the</strong> unequal spines<br />
A - Undersurface of leaf. B - Branch/ twig to show leaf arrangement. C- Detail<br />
of unequal spines.<br />
7
Figure 1.2 Flower <strong>and</strong> fruit of ber showing <strong>the</strong> pistil, stamens <strong>and</strong> seed<br />
A - Fruits on <strong>the</strong> tree. B - Vertical section through a mature fruit.<br />
C - Mature fruit. D - Stone/seed (from B/C). E - Vertical section through<br />
mature fruit - alternative variety. F - Mature fruit - alternative variety. G -<br />
Flower. H - Pistil. I - Pistil with stamens. J - Sepal. K - Petal.<br />
8
1.5 The minor cultivated species<br />
There are two species of Ziziphus which are still cultivated on a small scale.<br />
They are described below.<br />
1.5.1 Z. spina-christi (L.) Desf.<br />
Synonyms<br />
Z. africana Mill.<br />
Z. amphibia A. Chev.<br />
Z. nabeca (Forsk.) Lam.<br />
Z. inermis A. Chev.<br />
Z. sphaerocarpa Tul.<br />
Z. spina-christi Willd. (as used by Bailey, 1947 <strong>and</strong> Polunin <strong>and</strong> Huxley,<br />
1965).<br />
Shrub, often with intertwined branches, or small tree up to 10-15 m tall. Bark<br />
deeply furrowed <strong>and</strong> scaly, white-brown to pale grey. Branchlets densely<br />
pubescent white when young. Fruiting branchlets are not deciduous. Tends to<br />
produce a very deep tap root. Mostly spinous with paired spines, unequal in<br />
length, one recurved; rarely unarmed.<br />
Leaves ovate-lanceolate or ovate-elliptic (
Z. spina-christi is a species of <strong>the</strong> Middle East through Arabia <strong>and</strong> West Africa<br />
to N. E. Africa, Ethiopia <strong>and</strong> Eastern Africa, especially <strong>the</strong> drier tropical areas.<br />
It is wild in <strong>the</strong> Middle East, especially Iran, Saudi Arabia <strong>and</strong> also far<strong>the</strong>r west<br />
in Turkey. Its edible fruits are ga<strong>the</strong>red <strong>for</strong> food. Almost certainly it was<br />
introduced to Africa by Arab traders along <strong>the</strong> Mediterranean coast <strong>and</strong> also via<br />
<strong>the</strong> Horn of Africa. Its links to African homesteads were maintained because of<br />
its value as a shade tree, its use <strong>for</strong> fruits <strong>and</strong> its many <strong>o<strong>the</strong>r</strong> uses (von Maydell,<br />
1986; von Sengbusch <strong>and</strong> Dippolo, 1980). It is known to be a minor cultivated<br />
plant in India <strong>and</strong> Pakistan <strong>and</strong> more importantly in Egypt, Syria, <strong>the</strong> Mahgreb,<br />
Saharan oases <strong>and</strong> Zanzibar. This species is of interest because it has probably<br />
hybridised with Z. mauritiana according to in<strong>for</strong>mation from Pakistan,<br />
Dahomey <strong>and</strong> Nigeria. Also it can survive with half <strong>the</strong> annual rainfall needed<br />
by Z. jujuba <strong>and</strong> <strong>for</strong> both major cultivated species could be a source of drought<br />
resistance. The species prefers hot tropical or subtropical climates with low to<br />
medium rainfall <strong>and</strong> altitudes usually to 1500 m.<br />
Z. spina-christi is <strong>the</strong> species which is thought to have been used to make <strong>the</strong><br />
crown of thorns <strong>for</strong> Christ. However this is not certain because Paliurus spinachristi<br />
Mill. (syn. P. aculeatus Lam.) has also been proposed. The latter species<br />
is very similar to <strong>the</strong> jujube but has dry fruits with a broad orbicular horizontal<br />
wing. It is distributed in maquis, roadsides <strong>and</strong> waste places, similar to places<br />
where Z. spina-christi is naturalised. It extends from S.E. Europe to <strong>the</strong> Levant<br />
eastwards to <strong>the</strong> Himalayas <strong>and</strong> China. It too is a shrub, often spreading, or a<br />
small tree to 8-10 m, spinous in <strong>the</strong> same way, but <strong>the</strong> leaves <strong>and</strong> young twigs<br />
are glabrous (Polunin <strong>and</strong> Huxley, 1965).<br />
1.5.2 Z. lotus (L.) Lam.<br />
Synonyms<br />
Z. nummularia Aubrev.<br />
Z. saharae Blatt. & Trab.<br />
Z. lotus (L.) Desf. subsp. saharae Maire<br />
Z. sylvestris Mill.<br />
Z. parviflora Del.<br />
This species is a spiny shrub growing up to 1.5 m tall <strong>and</strong> resembling Z. jujuba.<br />
However, fruiting branchlets are not deciduous <strong>and</strong> twigs are grey. Internodes<br />
on branchlets are less than 1 cm long. Leaves are suborbicular or broadly<br />
elliptic to ovate, shallowly gl<strong>and</strong>ular-crenate, pubescent beneath <strong>and</strong> less so<br />
above; size (0.5-)1.2(-1.5) cm long x (0.4-)1(-1.3) cm broad.<br />
Flowers are solitary or 2(-3) toge<strong>the</strong>r.<br />
Fruits are subglobose fleshy drupes about 1 cm diameter <strong>and</strong> deep yellow.<br />
10
Z. lotus occurs from Asia Minor, south to Arabia, Egypt <strong>and</strong> along <strong>the</strong> North<br />
African coast <strong>and</strong> it reaches Cyprus <strong>and</strong> Greece in Europe. It is also cultivated<br />
in S. Portugal <strong>and</strong> Spain, parts of Italy <strong>and</strong> Sicily <strong>and</strong> in Provence, France. This<br />
is <strong>the</strong> lotus fruit of <strong>the</strong> Lotus eating people of Tunisia/Libya referred to by<br />
Homer, Herodotus, Polybius <strong>and</strong> <strong>o<strong>the</strong>r</strong> ancient writers.<br />
Z. lotus is of interest in rehabilitating certain degraded areas of N. Africa <strong>and</strong><br />
elsewhere in <strong>the</strong> eastern range of <strong>the</strong> species. Also European selections may fill<br />
niche markets.<br />
In relation to improvement of Indian jujube, Z. lotus could be used in respect to<br />
earliness of fruit maturity as well as drought tolerance, if hybridisation was<br />
initiated, especially between cultivars. Some confusion exists between Z. lotus<br />
<strong>and</strong> wild Z. nummularia of India, but <strong>the</strong>y are distinct. The eastern limits of Z.<br />
lotus need examining in <strong>the</strong> field.<br />
1.6 Wild species<br />
1.6.1 Asia<br />
There are numerous wild species of Ziziphus in Asia <strong>and</strong> <strong>the</strong>y tend to cluster in<br />
two regions: China <strong>and</strong> <strong>the</strong> Indian subcontinent. There are 14 species in China.<br />
Those, like Z. jujuba, belonging to Section Ziziphus of <strong>the</strong> genus are to be<br />
found mostly in <strong>the</strong> central <strong>and</strong> lower parts of <strong>the</strong> Huanghe River valley<br />
although <strong>the</strong> primary centre of diversity in China <strong>for</strong> Ziziphus species is south<br />
Yunnan <strong>and</strong> <strong>the</strong> sou<strong>the</strong>ast of Guangxi Province.<br />
Pareek (2001) noted <strong>the</strong> distribution of wild <strong>and</strong> naturalised Z. mauritiana<br />
throughout <strong>the</strong> greater part of India from <strong>the</strong> lowl<strong>and</strong>s to 1500 m in <strong>the</strong><br />
Himalayas <strong>and</strong> also in Sri Lanka. It is associated with dry areas where tree<br />
types can be found or bushy types in grassl<strong>and</strong>s. Early writings on <strong>the</strong> botany<br />
of India recorded <strong>the</strong> species as wild in <strong>the</strong> Siwalik <strong>for</strong>ests east of <strong>the</strong> Ganges<br />
<strong>and</strong> in <strong>for</strong>ests of Central India (Br<strong>and</strong>is, 1906). Z. jujuba, often recorded as Z.<br />
rugosa, can be found naturalised in <strong>the</strong> central <strong>and</strong> eastern sub-Himalayan<br />
region east to Bangladesh as well as in many <strong>o<strong>the</strong>r</strong> parts of India such as <strong>the</strong><br />
Central Provinces <strong>and</strong> western side of <strong>the</strong> Peninsula. O<strong>the</strong>r species cluster in<br />
<strong>the</strong> north west desert region of India <strong>and</strong> only a few in <strong>the</strong> Himalayas.<br />
In <strong>the</strong> drier parts of N. W. India, Z. nummularia (Burm. F.) Wight <strong>and</strong> Arn.<br />
(syn. Z. rotundifolia Lam.) was recognised by <strong>the</strong> Indian National Genetic<br />
Resources Programme as a species worthy of fur<strong>the</strong>r research. This was<br />
identified at an International Workshop on Maintenance <strong>and</strong> Evaluation of Life<br />
Support Species in Asia <strong>and</strong> <strong>the</strong> Pacific, held in New Dehli in April 1987. It is<br />
also a useful rootstock. The species is a thorny shrub producing red, edible<br />
fruits.<br />
11
Some wild species with wide distributions, such as Z. oenoplia Mill., have<br />
become weedy in places such as India, Sri Lanka, Myanmar or Malaysia.<br />
According to <strong>the</strong> literature, a few additional wild species cluster in Malaysia<br />
(Ridley, 1922) <strong>and</strong> also in Indonesia (Martin et al., 1987). However wild<br />
species from countries such as India, Myanmar <strong>and</strong> Malaysia or Myanmar<br />
eastwards through IndoChina have not been studied in a comparative way <strong>and</strong><br />
it is likely <strong>the</strong>re is a degree of synonymy to be clarified.<br />
Three <strong>o<strong>the</strong>r</strong> species need mention since <strong>the</strong>y are sometimes used as rootstocks.<br />
Z. xylopyra Willd. (syn. Z. rotundifolia Roth., Z. cuneata Wall.) is an erect,<br />
small tree frequently unarmed <strong>and</strong> producing a woody, inedible fruit. It is a<br />
species of South India <strong>and</strong> Sri Lanka. Z. rugosa Lam. is a straggly bush tending<br />
to have solitary spines <strong>and</strong> edible fruit, found in <strong>the</strong> Central Hills <strong>and</strong> eastern<br />
parts of India. Z. oenoplia Mill. is a scrambling shrub with spines <strong>and</strong> small<br />
black fruits often used <strong>for</strong> tanning <strong>and</strong> found in S. India, Sri Lanka <strong>and</strong><br />
Myanmar.<br />
1.6.2 Africa<br />
The <strong>o<strong>the</strong>r</strong> wild species in <strong>the</strong> Old World centre on Africa. Those covering very<br />
wide areas are Z. abyssinica Hochst. ex A. Rich. in scattered tree grassl<strong>and</strong><br />
400-2200 m from Senegal to Ethiopia <strong>and</strong> south to Zimbabwe <strong>and</strong><br />
Mozambique; Z. mucronata Willd. grows in open woodl<strong>and</strong> from 0-200 m<br />
above sea level from Senegal to Arabia <strong>and</strong> south to S. Africa <strong>and</strong> Madagascar;<br />
<strong>and</strong> Z. spina-christi in disturbed areas from 0-1300 m <strong>and</strong> is indigenous in<br />
semi-desert wadis from 600-1000 m above sea level in <strong>the</strong> Horn of Africa <strong>and</strong><br />
North Africa. Elsewhere in East Africa it was probably introduced <strong>and</strong> has<br />
become naturalised along roadsides in many parts of Africa <strong>and</strong> through seed<br />
propagation has often reverted from introduced cultivars to wild types.<br />
1.6.3 New World<br />
The few indigenous species are not discussed since <strong>the</strong>y are of minor relevance<br />
to <strong>the</strong> species dealt with in this <strong>monograph</strong>.<br />
1.7 Vernacular names <strong>for</strong> jujubes<br />
Vernacular names frequently refer only to a jujube fruit; in <strong>o<strong>the</strong>r</strong> cases different<br />
cultigens are identified. Table 1.1 provides names used in different regions,<br />
countries <strong>and</strong> languages, with reference to Indian <strong>and</strong> Chinese jujubes.<br />
12
Table 1.1 Vernacular names <strong>for</strong> jujubes<br />
Region Country Name (language in paren<strong>the</strong>ses)<br />
Asia Afghanistan <strong>Ber</strong>ra (Pashto)<br />
Bangladesh Bozoi, Kool, Kul<br />
Cambodia Putrea<br />
China Hong tsao, Lang tsao, Ta tsao, Tsao tse<br />
India Bogori (Assamese); Kul (Bengali); <strong>Ber</strong>, Bor, Bordi,<br />
Boyed (Gujarati); <strong>Ber</strong>, <strong>Ber</strong>i (Hindi); Badari, Baer,<br />
Bogari, Bore, Egasi, Elasi, Ilanji, Ilisi, Jelachi,<br />
Karkh<strong>and</strong>hu, Yolachi (Kannada); <strong>Ber</strong>, Bhor, Baher,<br />
Bor, Bardi, Bora (Marathi); Badaram, Badari, Kolam,<br />
Lantu, El<strong>and</strong>a, Perintutati (Malayadam); <strong>Ber</strong>, <strong>Ber</strong>i,<br />
Unals (Punjabi); Ajapriya, Badari, Balastha,<br />
Dridhabija, Dviparni, Ghonta, Gudaphala, Kantaki,<br />
Karkaramadhu, Koli, Kuvali, Madhuraphala,<br />
Madadebara, Nakhi, Nripabadari, Nripeshta,<br />
Prithukoli, Phalashayashira, Rajabadari, Rajakoli,<br />
Rajavallabha, Sukshmaphala, Sukshmapatrika,<br />
Srigalakoli, Svachha, Sukorapriya, Suphala, Tanubija,<br />
Ubhayakantaka (Sanskrit); <strong>Ber</strong>, Jangri (Sindhi);<br />
Adidarum, Attiram, Il<strong>and</strong>ai, Iradi, Koli, K<strong>and</strong>ai,<br />
Kullari, Kulvali, Padari, Sivagam, Vadari, Vettiram,<br />
Veyam, El<strong>and</strong>a (Tamil); Badaramu, Badari,<br />
Gangaregu, Gangarenu, Karkh<strong>and</strong>uvu, Regu, Renu<br />
(Telugu); <strong>Ber</strong> (Urdu); Barholi, Bodokoli, Bodori, Koli<br />
(Uriya)<br />
Africa<br />
Indonesia<br />
Iran<br />
Iraq<br />
Japan<br />
Laos<br />
Malaysia<br />
Myanmar<br />
Nepal<br />
Pakistan<br />
Philippines<br />
Sri Lanka<br />
Thail<strong>and</strong><br />
Vietnam<br />
Ethiopia<br />
Kenya<br />
Malawi<br />
Widara, Dara, Bidaru<br />
Kanar, Kunar, Nabik<br />
Aunnaberhindi, Nabig, Sidr<br />
Sanebuto-Natsume<br />
Than<br />
Bidaru, Epal siam, jujube<br />
Zi, Zee-pen, Zizidaw, Ziben<br />
Baer<br />
<strong>Ber</strong> (Urdu); <strong>Ber</strong>, <strong>Ber</strong>warter, Kunar (Baluchi)<br />
Manzanites, Manzanas<br />
Il<strong>and</strong>a, Mahadebara, Masaka (Sinhalese)<br />
Phutsa, Putsa, Man tan<br />
Tao, Tao-nhuc<br />
Abateri, Gaba-artgie, Gewa-ortigi (Tigre)<br />
Mkunazi (Swahili); Kwkurrah (Borao); Ekalati<br />
(Turhana); Olongo (Luo); Tolumuro (Pokot)<br />
Masawo (Chewa); Msondoka (Yao)<br />
13
Region Country Name (language in paren<strong>the</strong>ses)<br />
Somalia<br />
Sudan<br />
Tanzania<br />
Ug<strong>and</strong>a<br />
Zaire<br />
Zambia<br />
O<strong>the</strong>rs<br />
Zimbabwe<br />
West Africa<br />
<strong>and</strong> Sahel<br />
Language<br />
English<br />
French<br />
Greek<br />
Italian<br />
Portuguese<br />
Spanish<br />
Gob, Bheb, Jujuba<br />
Sidr nabk, Nabbag elfil,<br />
Mkunazi (Swalihi)<br />
Esilang (Karamajong)<br />
Kankole<br />
Masau (Nyanja); Musawce (Tonga); Akasongole<br />
(Bemba)<br />
Masua, Yanja, Musawu (Central Shona, Tangu);<br />
Domo, Ntomono, Surgo ntomono, Tomboro,<br />
Tomonou (Bambara); Batenluongu, Bu sakonhionabu<br />
Inakpayuani, Nan janlwane (Gourmanche); Magaria<br />
(Haussa); Magunuga, Mugulga, Mugulanga,<br />
Muegunga, Mugunuga, Mug-niga (More); Djabe,<br />
Djabi, Tabi, N’giobi (Peulh); Ngit (Sere); Ajzen<br />
(Tamachek); Dem, Dim, Sedem (Wolof).<br />
Name<br />
Jujube; Indian jujube, Indian plum, Indian cherry,<br />
Indian date; Chinese jujube; Chinese date; Chinese<br />
fig; Cottony jujube.<br />
Jujubier; (Le jujube d’ Afrique tropicale); Datte<br />
chinoise.<br />
Tzintzola<br />
Guiggiolo<br />
Jujubeira, Maceira<br />
Azufaifo, Yuyuba<br />
Sources: FAO, 1988; von Maydell, 1986; Pareek 2001; Sundararaj <strong>and</strong><br />
Balasubramanyam 1959; <strong>and</strong> editors.<br />
1.8 Historical evidence<br />
1.8.1 Indian jujube<br />
<strong>Ber</strong> has been recognised as a useful edible fruit since antiquity in India <strong>and</strong><br />
Watt, (1893) referred to this from references in ancient Sanskrit sources.<br />
Macdonell <strong>and</strong> Keith (1958) noted mention of ber in Vedic sources such as <strong>the</strong><br />
Yajurved. Pareek (2001) summarised <strong>the</strong> references to ber <strong>and</strong> <strong>o<strong>the</strong>r</strong> jujubes in<br />
scriptural sources <strong>and</strong> <strong>the</strong>se references covered <strong>the</strong> period from 1000 BC- 400<br />
AD.<br />
Such historical evidence attests to <strong>the</strong> recognition of <strong>the</strong> fruit <strong>and</strong> its uses; it<br />
does not imply domestication. Numerous writers state that ber has been in use<br />
<strong>for</strong> almost 4000 years in India. However, if <strong>the</strong> original wild species was<br />
spread from India through Myanmar <strong>the</strong>n early domestication ef<strong>for</strong>ts would<br />
14
postdate that of <strong>the</strong> staple foods <strong>and</strong> possibly occurred when populations<br />
increased with <strong>the</strong> rise of tribal kingdoms across <strong>the</strong> Gangetic plains.<br />
Excavations relating to <strong>the</strong> early Indus civilisation produced stones of Chinese<br />
jujube (see below) <strong>and</strong> later cultural links of people with <strong>the</strong> Mauryan empire<br />
would have resulted in cultural appreciation of jujubes, whatever <strong>the</strong> species.<br />
Scriptures mention both Z. mauritiana <strong>and</strong> Z. jujuba <strong>and</strong> even <strong>the</strong> wild Z.<br />
nummularia (Majumdar, 1945).<br />
<strong>Ber</strong> must have been widely appreciated because excavations at Navdatoli-<br />
Maheshwar on <strong>the</strong> Deccan plateau produced ber stones from almost certainly<br />
ga<strong>the</strong>red wild fruits. They date to 3500-3000 BP predating <strong>the</strong> Gangetic<br />
civilisation. This area is one where ber is thought to have been truly wild.<br />
(Mittre, 1961; Sankalia, 1958; Pareek 2001).<br />
Once cultivated, ber would have been moved with historical migrations of<br />
people <strong>and</strong> <strong>the</strong>ir trade. It is thought to have been in Africa <strong>for</strong> only a few<br />
centuries <strong>and</strong> it is likely that introduction to China <strong>and</strong> Indonesia is also fairly<br />
recent. Introduction to Australia was to Queensl<strong>and</strong> <strong>and</strong> <strong>the</strong> Nor<strong>the</strong>rn Territory<br />
late in <strong>the</strong> nineteenth century (Grice, 1998).<br />
1.8.2 Chinese jujube<br />
The area where Z. jujube was domesticated is almost certainly in <strong>the</strong> Yellow<br />
River area. The Yellow River – Huaihe River plain is <strong>the</strong> main area <strong>for</strong> this<br />
species today with much of <strong>the</strong> cultivated production in Henan, Shanxi <strong>and</strong><br />
Sh<strong>and</strong>ong provinces. It is thought to have been taken into cultivation about<br />
2000 BP, probably early Shang dynasty of <strong>the</strong> Bronze Age. It is mentioned in<br />
<strong>the</strong> Book of Songs, a poem of <strong>the</strong> tenth century BP (Qu, 1983).<br />
The progenitor wild species has a very wide area of distribution from China to<br />
Pakistan <strong>and</strong> wild fruit would have been ga<strong>the</strong>red in many areas. Excavations<br />
indicate that people of <strong>the</strong> earliest farming settlements of <strong>the</strong> Indus valley<br />
civilization at Mehrgar in Balluchistan collected fruits (excavations dates<br />
seventh millennium BP). This continued as evidenced by similar finds from<br />
Pirah, Pakistan from <strong>the</strong> later unified Indus culture (Zohary <strong>and</strong> Hopf, 1988).<br />
Vavilov (1951) considered <strong>the</strong> primary centre of origin to be wider than China<br />
<strong>and</strong> <strong>the</strong> cultivation must have spread quickly through Central Asia. Impetus<br />
could have related to its carriage along <strong>the</strong> old trade routes <strong>and</strong> <strong>the</strong> later<br />
Mongol empires. Kazvini writing in <strong>the</strong> nineteenth century AD mentioned <strong>the</strong><br />
excellent jujubes in <strong>the</strong> Province of Jurjan of <strong>the</strong> Abbasid Caliphs. Jurjan is<br />
located around <strong>the</strong> border between N. E. Persia <strong>and</strong> S. Turkmenistan. He wrote<br />
that trees fruited twice a year <strong>and</strong> at 2 – 3 years old (Le Strange, 1930). This<br />
particular area was linked to <strong>the</strong> trade routes from China to <strong>the</strong> Mediterranean<br />
as well as to <strong>the</strong> Indus valley. Chinese jujube was thought to have reached SW<br />
15
Asia by 2000-3000 BP (de C<strong>and</strong>olle, 1886). It was taken, according to Pliny,<br />
from <strong>the</strong> Levantine Coast to Europe in <strong>the</strong> time of Augustus by <strong>the</strong> Consul<br />
Sextus Popinus. It is thought to have been spread along <strong>the</strong> North African coast<br />
in <strong>the</strong> seventh century AD.<br />
In relation to West Asia a number of excavations have found remains of jujube<br />
fruits linked to numerous Neolithic <strong>and</strong> Bronze Age sites (Zohary & Hopf,<br />
1988); Egypt 4000 BC (Montet cited by Munier, 1973); also from shell<br />
middens near Muscat, Oman from <strong>the</strong> fourth millennium BC (Biagi <strong>and</strong> Nisbet,<br />
1992). It is most likely <strong>the</strong>se ga<strong>the</strong>red fruits were of Z. spina-christi or Z. lotus.<br />
Chinese jujube has however developed a secondary centre of diversity in West<br />
Asia <strong>and</strong> is naturalised in many areas such as along <strong>the</strong> Black Sea Coast (Tutin,<br />
1968).<br />
Chinese jujuba was first introduced from Europe to USA in 1837 by Robert<br />
Chisholm <strong>and</strong> planted in Beau<strong>for</strong>t, South Carolina <strong>and</strong> introduced to Cali<strong>for</strong>nia<br />
<strong>and</strong> neighbouring states from sou<strong>the</strong>rn France by Rix<strong>for</strong>d in 1876, (Rix<strong>for</strong>d,<br />
1917). By 1901 jujube had escaped from cultivation in Alabama (Mohr, 1901)<br />
<strong>and</strong> is now naturalised along <strong>the</strong> Gulf Coast from Alabama to Louisiana<br />
(Bonner <strong>and</strong> Rudolf, 1971).<br />
All of <strong>the</strong> early jujube introductions into <strong>the</strong> United States were seedlings from<br />
Europe, <strong>and</strong> it was not until 1908 that <strong>the</strong> much superior Chinese cultivars<br />
began to be introduced (Lyrene, 1979). In that year Frank Meyer, a US<br />
Department of Agriculture plant explorer, introduced Lang <strong>and</strong> <strong>o<strong>the</strong>r</strong> Chinese<br />
cultivars (Lanham, 1926; Meyer, 1911). A second group of cultivars introduced<br />
in 1914 included Li, which produced <strong>the</strong> largest fruit he had seen in China<br />
(Lanham, 1926). In recent years Russian cultivars have been introduced to<br />
boost an improvement programme at <strong>the</strong> Alabama ADM University.<br />
In <strong>the</strong> twentieth century superior Chinese materials were introduced to Japan,<br />
<strong>and</strong> also to North Africa by French scientists.<br />
The Chinese jujube (Z. jujube) has been introduced into more than 30 countries<br />
(Liu et al., 2003a) <strong>and</strong> is becoming increasingly popular <strong>for</strong> its wide<br />
adaptations, easy management, early bearing, rich nutrition <strong>and</strong> multiple uses.<br />
Z. jujuba (Z. mauritiana) was brought to <strong>the</strong> non-French West Indies from<br />
India <strong>and</strong> Indonesia during <strong>the</strong> colonial period (Barbeau, 1994). In 1993, 160<br />
seeds of <strong>the</strong> leading varieties of tomentose jujube (Z. mauritiana) grown in<br />
Burma (Myanmar) were introduced to China. Plants were vigorous <strong>and</strong><br />
matured very early. Two promising varieties were selected, <strong>the</strong> fruits of which<br />
are crisp, tender, sweet <strong>and</strong> of very good eating quality (Liub, 1997).<br />
The introduction of Z. mauritiana to <strong>the</strong> Negev desert of Israel has been found<br />
most promising (Nerd et al., 1990). ‘Taiwan Cuizao’ was introduced in 1997<br />
16
(Xue <strong>and</strong> Xue, 2001). Six Z. jujuba (Z. sativa) cultivars were introduced into<br />
Macedonia from USSR (Ristevski et al., 1982) which were found to be<br />
resistant to low winter <strong>and</strong> high summer temperatures. Introduction of Z.<br />
mauritiana was found to grow satisfactorily under <strong>the</strong> conditions of <strong>the</strong> Jordan<br />
Valley, Negev <strong>and</strong> Arava areas <strong>and</strong> to produce fruits of commercial value<br />
(Mizrahi et al. 1991). Fruit trees suitable <strong>for</strong> introduction to desert areas of<br />
Israel have been described by Mizrahi et al., (2002). Wushizhong is a<br />
cultivated variety of Ziziphus mauritiana, introduced from Taiwan. It flowers<br />
twice a year (in May-July <strong>and</strong> early September), but spring flowers do not<br />
result in much fruit setting. The main production is produced by autumn<br />
flowers.<br />
17
2.1 Introduction<br />
Chapter 2. Composition<br />
C. Bowe<br />
Species of Ziziphus are considered to be multipurpose plants although use of<br />
<strong>the</strong> fruits is <strong>the</strong> major focus of interest. They are of increasing use in<br />
agro<strong>for</strong>estry. The composition of <strong>the</strong> fruits is <strong>the</strong>re<strong>for</strong>e of importance especially<br />
since <strong>the</strong>y are produced by a limited number of species which have been<br />
cultivated <strong>for</strong> millennia.<br />
There is a great deal of published data on <strong>the</strong> potential of <strong>the</strong> species <strong>for</strong><br />
ethnobotanical uses (Arndt <strong>and</strong> Kayser, 2001). Pareek (2001) noted that<br />
although different parts of <strong>the</strong> plant have medicinal value due to <strong>the</strong>ir<br />
constituents <strong>the</strong>ir usage appears to be sporadic <strong>and</strong> not commonplace.<br />
This chapter looks in particular at <strong>the</strong> nutritive composition of fruits <strong>and</strong> <strong>the</strong>n<br />
provides a summary of <strong>the</strong> more important ethnopharmacological compounds<br />
<strong>and</strong> <strong>the</strong>ir properties, when known.<br />
2.2 Fruit composition<br />
2.2.1 <strong>Ber</strong><br />
Much of <strong>the</strong> data relating to ber fruits are cultivar specific; however <strong>the</strong><br />
in<strong>for</strong>mation can be summarised to provide a general picture. The pulp of <strong>the</strong><br />
fruits is of most importance in relation to nutrition. Pareek (1983) recorded<br />
fresh, mature with 81-97 % pulp <strong>and</strong> Jaw<strong>and</strong>a et al., (1980a,b) considered <strong>the</strong><br />
range 91.6-92.9 %.<br />
The constituents of <strong>the</strong> pulp are shown in table 2.1<br />
18
Table 2.1 Nutritional constituents in fruit pulp of 4 ber cultivars<br />
Constituents Gola Kaithli Banarsi Umran<br />
Karaka<br />
Moisture (%) 81 -- 81 --<br />
Starch (%) 0.95 -- 0.86 --<br />
TSS ( o Brix) 17-20 16-18 13-17 18-20<br />
Total sugars (%) 8.3-12.1 4.9-10 5.4-12.4 7.2-7.4<br />
Reducing sugars (%) 3.3-5.8 1.95-2.7 3.3-3.7 2.6-2.9<br />
Non-reducing sugars (%) 2.4-8.4 2.2-8.0 3.3-8.4 4.8-4.9<br />
Acidity (%) 0.37-0.75 0.16-0.51 0.13-0.48 0.19-0.35<br />
Protein (%) - 1.18 - 1.03<br />
Total ash (%) - 0.45 - 0.34<br />
CaO (%) - 0.04 - 0.03<br />
P 2 O 5 (%) - 0.02 - 0.01<br />
Fe 2 O 3 (mg/100g) - 0.5 - 1.00<br />
Ascorbic acid (mg/100g) 70 89-133 66-110 73-103<br />
(Source: Pareek, 1983).<br />
The richness of <strong>the</strong> pulp in nutritive compounds has been widely recognised.<br />
None<strong>the</strong>less <strong>the</strong>re are no definitive values <strong>for</strong> pulp composition. However ber<br />
is richer than apple in protein, phosphorus, calcium, carotene <strong>and</strong> Vitamin C<br />
(Bakhshi <strong>and</strong> Singh, 1974) <strong>and</strong> oranges in phosphorus, iron, vitamin C <strong>and</strong><br />
carbohydrates <strong>and</strong> exceeds <strong>the</strong>m in calorific value. Ripe fruits provide 20.9<br />
Kcalories per 100 g of pulp (Singh et al., 1973a).<br />
In terms of carbohydrates, pulp contains 12.8 – 13.6 % (Singh et al., 1967);<br />
(Jaw<strong>and</strong>a et al., 1981) of which 5.6 % is sucrose, 1.5 % glucose, 2.1 % fructose<br />
<strong>and</strong> 1 % starch. Total sugars content is markedly different according to cultivar<br />
(Singh et al., 1983a).<br />
The amino acids asparagine, aspartic acid, glycine, glutamic acid, serine, á-<br />
serine <strong>and</strong> threonine, are found in <strong>the</strong> pulp (Bal, 1981a) but not many analyses<br />
or comparisons have been made.<br />
Major interest has focused on Vitamin C content <strong>and</strong> ber pulp is considered a<br />
rich source. Content ranges from 70-165 mg/100 g (Bal <strong>and</strong> Mann, 1978). The<br />
FAO <strong>and</strong> WHO recommendation (FAO, 1974) that <strong>the</strong> daily intake <strong>for</strong> an adult<br />
man should be 30 mg, illustrates <strong>the</strong> value of ber pulp in <strong>the</strong> diet.<br />
Pulp contains about 70 IU Vitamin A /100 g <strong>and</strong> <strong>the</strong> ß-carotene content ranges<br />
from 75 to more than 80 mg/100 g (Bal et al., 1978).<br />
19
2.2.2 Chinese jujube<br />
Pareek (2001) gave details of <strong>the</strong> composition of Chinese jujube pulp from a<br />
number of sources. They include 9.6 – 33 % sugars, 0.3 – 2.5 % acids<br />
especially succinic <strong>and</strong> malic; (Ahmedov <strong>and</strong> Halmatov, 1969), 2.9 % protein,<br />
<strong>and</strong> 136-363 mg/100 g of vitamin C. (Tasmatov, 1963; Baratov et al., 1975;<br />
Ristevski et al., 1982; Cireasa et al., 1984). Fruits average 28 – 40.3 % dry<br />
matter (Ristevski et al., 1982). Apart from Vitamin C, Chinese jujube are<br />
significant sources of minerals such as iron, phosphorus <strong>and</strong> calcium (Ming <strong>and</strong><br />
Sun, 1986), Vitamin B complex <strong>and</strong> Vitamin P (Troyan <strong>and</strong> Kruglyakov, 1972;<br />
Kuliev <strong>and</strong> Guseinova, 1974).<br />
Vitamin C content tends to decline as fruits ripen e.g. in cultivar Hamazhao it<br />
falls from 1096 to 411 mg/100 g pulp (Bi et al. 1990). It appears that Chinese<br />
jujube is a richer source of vitamin C than ber depending on <strong>the</strong> cultivar, which<br />
is a point of interest to plant breeders.<br />
Dried fruits of jujube contain volatile substances which help to impart <strong>the</strong><br />
typical flavour. Seventy eight such compounds have been identified in Z.<br />
jujuba var. inermis among which aliphatic acids <strong>and</strong> carbonyl compounds<br />
accounted <strong>for</strong> 62.97 % <strong>and</strong> 29.56 % of total volatiles (Wong et al., 1996). The<br />
major components were as follows.<br />
2.3 Ethnopharmaceutical compounds<br />
The bulk of <strong>the</strong> in<strong>for</strong>mation relates to Z. jujube <strong>and</strong> a summary is provided<br />
below because of its widespread use in Chinese Herbal <strong>and</strong> Yunani medicine.<br />
In numerous cases <strong>the</strong> same constituents are also found in ber.<br />
2.3.1 Ascorbic acid, thiamine, riboflavin <strong>and</strong> bioflavonoids<br />
Ziziphus jujuba fruits are very rich in vitamins C <strong>and</strong> B1 (thiamine) <strong>and</strong> B2<br />
(riboflavin) (Troyan <strong>and</strong> Kruglyakov, 1972; Kuliev <strong>and</strong> Guseinova, 1974).<br />
Compared with ber, one fruit per day would meet <strong>the</strong> diet requirements <strong>for</strong><br />
Vitamin C <strong>and</strong> Vitamin B complex of an adult man recommended by<br />
FAO/WHO. It is also known to have a high Vitamin P (bioflavonoid) content.<br />
In some fruits Baratov et al., (1975) reported 188 to 544 mg Vitamin C <strong>and</strong> 354<br />
to 888 mg Vitamin P per 100 g pulp. Ahmedov <strong>and</strong> Halmatov (1969) <strong>and</strong><br />
Troyan <strong>and</strong> Kruglyakov (1972) reported even higher contents of Vitamin C (up<br />
to 811 mg/100 g) <strong>and</strong> vitamin P (up to 1230 mg/100 g). Vitamin P<br />
(bioflavonoids) enhances <strong>the</strong> action of Vitamin C. Vitamin C <strong>and</strong> Vitamin P<br />
also act toge<strong>the</strong>r to help maintain <strong>the</strong> thin walls of capillaries. Vitamin P also<br />
has antibacterial, anti inflammatory <strong>and</strong> antioxidant properties, <strong>and</strong> is known to<br />
stimulate bile production, promote circulation <strong>and</strong> prevent allergies (GreatVista<br />
Chemicals, 2004).<br />
20
2.3.2 Pectin A<br />
Tomoda et al., (1985) isolated pectin A from Z. jujuba fruit. Pectin A was<br />
found to contain 2,3,6-tri-o-acetyl D lactose units. Pectin has a number of<br />
pharmaceutical properties such as binding bile acid, lowering plasma<br />
cholesterol <strong>and</strong> anti diarrhoeal properties (PDRHealth, 2004).<br />
2.3.3 Alkaloids<br />
Stem bark of Ziziphus species contain alkaloids (Pareek, 2001). A sapogenin,<br />
zizogenin has been isolated from Z. mauritiana stems (Srivastava <strong>and</strong><br />
Srivastava, 1979).<br />
The cyclic peptide alkaloids, mauritine-A, mucronine-D, amphibine-H,<br />
nummularine-A <strong>and</strong> -B (Tschesche et al., 1976), sativanine-A <strong>and</strong> sativanine-<br />
B, frangulanine, nummularine-B <strong>and</strong> mucronine were isolated from <strong>the</strong> bark of<br />
Z. jujuba by Tschesche et al. (1976, 1979) at <strong>the</strong> Institut für Organische<br />
Chemie und Biochemie, University of Bonn, Germany. This work was<br />
continued by Shah <strong>and</strong> his group (Shah et al., 1984 a; 1984 b; 1985a; 1986)<br />
who isolated <strong>the</strong> cyclic peptide alkaloids sativanine-C, sativanine-G,<br />
sativanine-E, sativanine-H, sativanine-F, sativanine-D <strong>and</strong> sativanine-K from<br />
Z. jujuba stem bark. The alkaloids coclaurine, isoboldine, norisoboldine,<br />
asimilobine, iusiphine <strong>and</strong> iusirine were isolated from Z. jujuba leaves by<br />
Ziyaev et al., (1977). Cyclopeptide <strong>and</strong> peptide alkaloids from Z. jujuba were<br />
found to show sedative effects (Han <strong>and</strong> Park, 1986).<br />
The seeds of Z. jujuba var. spinosa also contain cyclic peptide alkaloids<br />
sanjoinenine, franguloine <strong>and</strong> amphibine-D <strong>and</strong> four peptide alkaloids;<br />
sanjoinine-B-D-F <strong>and</strong> -G2 (Han et al., 1990). The seeds are used in Chinese<br />
medicine as a sedative.<br />
Chemical studies of Z. mauritiana led to <strong>the</strong> isolation of <strong>the</strong> cyclopeptide<br />
alkaloids, mauritines A <strong>and</strong> B; C-F, G <strong>and</strong> H, frangufoline; amphibines D, E, B<br />
<strong>and</strong> F; hysodricanin-A, scutianin-F <strong>and</strong> aralionin-C (Tschesche et al., 1972;<br />
1974; 1977). The cyclopeptide alkaloid, mauritine J, was isolated from <strong>the</strong> root<br />
bark of Z. mauritiana (Jossang et al., 1996).<br />
2.3.4 Glycosides<br />
2.3.4.1 Flavonoid glycosides/spinosins<br />
Woo et al., (1979) gave <strong>the</strong> structure of spinosin (2”-O- beta –<br />
glucosylswertisin) extracted from Z. jujuba var. spinosa seed. They later<br />
identified three acylated flavone-C-glycosides (6’’’-sinapoylspinosin, 6’’’-<br />
feruloylspinosin <strong>and</strong> 6’’’-p-coumaroylspinosin). All showed mild sedative<br />
activity in pharmacological tests. Zeng et al., (1987) discovered a new<br />
flavonoid, named zivulgarin, compound (4-beta-D-glycopyranosyl swetisin).<br />
21
2.3.4.2 Glycosides/saponins<br />
The glycoside saponin is found in <strong>the</strong> seeds, leaf <strong>and</strong> stem of Z. jujuba<br />
(Ogihara et al., 1976). Saponins are part of sugar chains which attach<br />
<strong>the</strong>mselves to a sterol or triterpene. They are known to bind with cholesterol<br />
preventing it from being reabsorbed into <strong>the</strong> system. They are being widely<br />
researched <strong>for</strong> cancer prevention <strong>and</strong> cholesterol control. Ogihara (1976)<br />
developed a method <strong>for</strong> successful qualitative <strong>and</strong> quantitative determination of<br />
saponins in Z. jujuba seeds using counter current chromatography.<br />
The saponins isolated from <strong>the</strong> seeds of Z .jujuba include jujubosides A, B<br />
(ZengL et al., 1987), A1 B1 <strong>and</strong> C <strong>and</strong> acetyljujuboside B (Yoshikawa et al.,<br />
1997) <strong>and</strong> <strong>the</strong> protojujubosides A, B <strong>and</strong> B1 (Matsuda et al., 1999).<br />
Kurihara et al. (1988) extracted <strong>the</strong> saponin, ziziphin, from <strong>the</strong> dried leaves of<br />
Z. jujuba. It has a structure, 3-O-a-L-rhamnopyranosyl (1-2)-a-Larabinopyranosyl-20-O-<br />
(2,3)-di-O-acetyl-a-L-rhamnopyranosyl jujubogenin.<br />
Ikram et al. (1981) isolated a saponin from Z .jujuba leaves <strong>and</strong> stem. It was<br />
assigned <strong>the</strong> structure 3-O- ((2-O- alpha – D – furopyranosyl – 3-O- beta – D –<br />
glucopyranosyl) – alpha – L – arabinopyranosyl) jujubogenin. Jujubogenin was<br />
also found in extract of Z. mauritiana leaves (Sharma <strong>and</strong> Kumar, 1982).<br />
Saponins show adjuvant (Oda et al., 2000), haemolytic (Oda et al., 2000),<br />
sedative (Shou et al., 2002) anxiolytic <strong>and</strong> sweetness inhibiting properties<br />
(Kurihara et al., 1988). Jujuboside A (JuA), is also known to be a noncompetitive<br />
inhibitor of calmodulin (Zhou et al., 1994), which is an ubiquitous,<br />
calcium-binding protein that can bind to <strong>and</strong> regulate a multitude of different<br />
protein targets, <strong>the</strong>reby affecting many different cellular functions. CaM<br />
mediates processes such as inflammation, metabolism, muscle contraction,<br />
short-term <strong>and</strong> long-term memory, <strong>and</strong> <strong>the</strong> immune response (McDowall,<br />
2003). Jujuboside inhibition of calmodulin is thought to be linked to its<br />
sedative properties (Zhou et al., 1994).<br />
2.3.5 Triterpenoic acids<br />
The following triterpenoic acids have been isolated from <strong>the</strong> fruits of Z. jujuba:<br />
colubrinic acid, alphitolic acid, 3-O-cis-p-coumaroylalphitolic acid, 3-O-transp-coumaroylalphitolic<br />
acid, 3-O-cis-p-coumaroylmaslinic acid, 3-O-trans-pcoumaroylmaslinic<br />
acid, oleanolic acid, betulonic acid, oleanonic acid,<br />
zizyberenalic acid <strong>and</strong> betulinic acid (Lee et al., 2003). Triterpenoic acids have<br />
shown cytotoxic effects on tumour cell lines (Eiznhamer <strong>and</strong> Xu, 2004).<br />
Triterpenoic acids have also been extracted from roots of Z. mauritiana (Kundu<br />
et al. 1989).<br />
22
2.3.5.1 Betulinic acid<br />
Betulinic acid is a naturally occurring pentacyclic triterpenoid which has<br />
demonstrated selective cytotoxicity against a number of specific tumour types.<br />
It has been found to selectively kill human melanoma cells while leaving<br />
healthy cells alive (Pisha et al., 1995; Kim et al., 1998) Betulinic acid has also<br />
been found to retard <strong>the</strong> progression of HIV 1 infection, by preventing <strong>the</strong><br />
<strong>for</strong>mation of syncytia (cellular aggregates). In addition, betulinic acid has been<br />
found to have anti-inflammatory activity (Kim et al., 1998) <strong>and</strong> antibacterial<br />
properties <strong>and</strong> inhibits <strong>the</strong> growth of both Staphylococcus aureus <strong>and</strong><br />
Eschericheria coli (Eiznhamer <strong>and</strong> Xu, 2004).<br />
2.3.5.2 Oleanolic acid<br />
Oleanolic acid also exhibits known antitumour activity (Hsu et al., 1997;<br />
Amsar Private Limited, 2004)<br />
2.3.6 Lipids<br />
Both <strong>the</strong> pericarp <strong>and</strong> <strong>the</strong> seeds of Z. jujuba contain two main classes of<br />
phospholipids: phosphatidylcholines <strong>and</strong> phosphatidylglycerols. Oleic acid is<br />
present in <strong>the</strong> fatty oil of <strong>the</strong> seeds (Goncharova et al., 1990). Bioactivityguided<br />
fractionation of petroleum e<strong>the</strong>r- EtOAc- <strong>and</strong> soluble extracts of <strong>the</strong><br />
seeds of Z. jujuba indicated that <strong>the</strong> triglyceride, 1,3-di-O-[9(Z)-octadecenoyl]-<br />
2-O-[9(Z),12(Z)-octadecadienoyl] glycerol, <strong>and</strong> a fatty acid mixture of linoleic,<br />
oleic <strong>and</strong> stearic acids, were <strong>the</strong> major active components of <strong>the</strong> seed oil. (Su et<br />
al., 2002).<br />
2.4 Nutritional <strong>and</strong> pharmaceutical studies<br />
2.4.1 Sweetness inhibitors<br />
Triterpenoid sweetness inhibitors were isolated from Z. jujuba. Extracts from<br />
<strong>the</strong> leaves of Z. jujuba have been found to suppress sweet taste sensation in fly<br />
(Pharma regina), rat <strong>and</strong> in hamster. Antisweet substances isolated from Z.<br />
jujuba included jujubasponins II, III, IV, V <strong>and</strong> VI <strong>and</strong> from <strong>the</strong> leaves,<br />
jujuboside B from <strong>the</strong> leaves <strong>and</strong> seeds <strong>and</strong> ziziphus saponins I-III from dried<br />
fruit. Ziziphin <strong>and</strong> jujubosaponins II <strong>and</strong> III, <strong>the</strong> only three of <strong>the</strong> anti-sweet<br />
saponins from this plant with acyl groups, were up to 4 times more active in<br />
suppressing <strong>the</strong> sweet taste of sucrose than <strong>the</strong> <strong>o<strong>the</strong>r</strong> anti-sweet constituents<br />
(Suttisri et al. 1995).<br />
The saponin, ziziphin extracted by Kurihara <strong>and</strong> Halpern (1988) suppressed <strong>the</strong><br />
sweetness induced by D-glucose, D-fructose, stevioside, glycine, sodium<br />
saccharin, aspartame <strong>and</strong> naringin dihydrochalcone. It however showed no<br />
suppressive effect on <strong>the</strong> sour taste of hydrochloric acid <strong>and</strong> <strong>the</strong> bitter taste of<br />
quinine indicating that ziziphin is highly specific to sweet taste (Kurihara,<br />
1992). Ziziphin was found to inhibit <strong>the</strong> sweet taste receptors in humans (Smith<br />
23
<strong>and</strong> Halpern, 1983). The mechanism which ziziphin used was identified as taste<br />
modification. On comparison with known gymnemic acids, effects suggest that<br />
net dissociation of ziziphins from taste receptor membranes <strong>and</strong>/or inactivation<br />
in <strong>the</strong> membrane may be much faster than with gymnemic acids. The<br />
compound is considered useful as a taste modifier resulting in reduced sugar<br />
intake <strong>and</strong> <strong>the</strong>reby reducing obesity in diabetic or overweight people (Suttisri et<br />
al., 1995).<br />
2.4.2 Permeability enhancement activity<br />
Delivery of certain classes of drugs such as peptides creates problems in<br />
transportation across cell membranes <strong>and</strong> subsequent diminished<br />
bioavailability. To overcome this barrier, permeability enhancers can be used to<br />
aid <strong>the</strong> passage of drugs across cell membranes. To assess <strong>the</strong> permeability<br />
enhancing activity of Z. jujuba, an aqueous extract of seeds was compared to<br />
two members of a known series of permeability enhancement agents belonging<br />
to <strong>the</strong> alkylglycosides. Cell culture systems were observed after transepi<strong>the</strong>lial<br />
electrical resistance (TEER) recorded <strong>the</strong> results of application of <strong>the</strong> three<br />
agents <strong>and</strong> changes in cell monolayer resistance. Lowering of resistance across<br />
a cell monolayer is an indication of ei<strong>the</strong>r <strong>the</strong> opening of tight junctions <strong>and</strong>/or<br />
<strong>the</strong> fluidisation of cell membranes. Z. jujuba extract lowered cell resistance<br />
more rapidly in a given time period than <strong>the</strong> alkylglycosides <strong>and</strong> allowed full<br />
recovery of cells in a relatively short time period. It appears that <strong>the</strong> extract of<br />
Z. jujuba may be more efficient as a permeability enhancer than <strong>the</strong> two<br />
alkylglycosides. It remains to fur<strong>the</strong>r analyse <strong>the</strong> extract to determine <strong>the</strong> active<br />
agent or agents (Eley <strong>and</strong> Hossein, 2002).<br />
2.4.3 Cytotoxic effect (chem<strong>o<strong>the</strong>r</strong>apy)<br />
The in vitro cytotoxicities of <strong>the</strong> triterpenoic acids extracted from Z. jujuba<br />
were tested against tumour cell lines . The lupane-type triterpenes showed high<br />
cytotoxic activities. The cytotoxic activities of 3-O-p- coumaroylalphitolic<br />
acids were found to be better than those of non-coumaroic triterpenenoids.<br />
These results suggest that <strong>the</strong> coumaroyl moiety at <strong>the</strong> C-3 position of <strong>the</strong><br />
lupane-type triterpene may play an important role in enhancing cytotoxic<br />
activity (Lee et al., 2003).<br />
The triterponic acid, betulinic acid, extracted from Z. jujuba <strong>and</strong> Z. mauritiana,<br />
showed selective toxicity against cultured human melanoma cells (Kim et al.,<br />
1998). Betulinic acid is currently undergoing preclinical development (Pisha et<br />
al., 1995). It is thought that betulinic acid may also be effective against <strong>o<strong>the</strong>r</strong><br />
types of cancer. Recently, considerable in vitro evidence has demonstrated that<br />
betulinic acid is effective against small- <strong>and</strong> non-small-cell lung, ovarian,<br />
cervical, <strong>and</strong> head <strong>and</strong> neck carcinomas. Published data suggest that betulinic<br />
acid induces apoptosis (Kim et al., 1998; Liu et al., 2004) in sensitive cells in a<br />
p53- <strong>and</strong> CD95-independent fashion (Eiznhamer <strong>and</strong> Xu, 2004).<br />
24
Oleanolic acid is known to have antitumour effects (Hsu et al., 1997; Amsar<br />
Private Limited, 2004) as well as <strong>the</strong> ability to decrease undesirable radiation<br />
damage to <strong>the</strong> hematopoietic tissue. after radi<strong>o<strong>the</strong>r</strong>apy (Hsu et al., 1997).<br />
Oleanolic acid has been recommended <strong>for</strong> skin cancer <strong>the</strong>rapy in Japan (Muto<br />
et al., 1990). Cosmetic preparations <strong>for</strong> <strong>the</strong> prevention of tropical skin cancer<br />
containing oleanolic acid have been patented (Ishida et al., 1990).<br />
2.4.4 Neurological properties<br />
2.4.4.1 Hypnotic-sedative <strong>and</strong> anxiolytic effect<br />
The seeds <strong>and</strong> leaves of many Ziziphus species have been found to have<br />
anxiolytic <strong>and</strong> hypnotic-sedative effects. They are known to depress activity of<br />
<strong>the</strong> central nervous system which reduces anxiety <strong>and</strong> induces sleep. Saponins<br />
<strong>and</strong> flavonoids from Z. jujuba seeds were examined <strong>for</strong> sedative activity. All<br />
compounds tested showed sedative <strong>and</strong> hypnotic effects. Swertisin, <strong>the</strong> most<br />
potent compound was tested <strong>for</strong> type of action. It was found that it produced<br />
sleep, but was not anticonvulsant or muscle relaxant (Peng et al., 2000).<br />
The saponin jujuboside A (JuA), <strong>the</strong> main component of jujubogenin extracted<br />
from <strong>the</strong> seed of Z. jujuba is widely used in Chinese traditional medicine <strong>for</strong><br />
<strong>the</strong> treatment of insomnia <strong>and</strong> anxiety. A combined research group at <strong>the</strong><br />
College of Life Science <strong>and</strong> <strong>the</strong> Department of Biomedical Engineering at<br />
Zhejiang University, China, used in vivo (Shou et al., 2002) <strong>and</strong> in vitro (Shou<br />
et al., 2001; Feng <strong>and</strong> Zheng, 2002; Shou et al., 2002) methods, to investigate<br />
<strong>the</strong> inhibitory effects of Jujuboside A (JuA) on rat hippocampus.<br />
Peng <strong>and</strong> his colleagues also demonstrated <strong>the</strong> anxiolytic effects in mice of a<br />
polyherbal substance containing seed extract of Z. jujuba (Lin et al., 2003).<br />
Alkaloids from Z. jujuba were also found to show sedative activity. Both<br />
sanjoinine A <strong>and</strong> nuciferine prolonged <strong>the</strong> sleeping time produced by<br />
hexobarbital. When sanjoinine was heated it was found to produce an isomer of<br />
even greater sedative effect (Han <strong>and</strong> Park, 1986).<br />
2.4.4.2 Cognitive activities<br />
Heo et al. (2003) suggests that oleamide, a component of Z. jujuba extract,<br />
could be a useful chemo-preventative agent against Alzheimer’s disease. They<br />
found that methanolic Z. jujuba showed 34.1 % activation effect on choline<br />
acetyltransferase in vitro, an enzyme that controls <strong>the</strong> production of<br />
acetylcholine which appears to be depleted in <strong>the</strong> brains of Alzheimer patients.<br />
Using sequential fractionation <strong>the</strong> active ingredient was found to be cis-9-<br />
octadecenoamide (oleamide) which showed 65% activation effect.<br />
Administration of oleamide to mice significantly reversed <strong>the</strong> scopolamineinduced<br />
memory <strong>and</strong>/or cognitive impairment in <strong>the</strong> passive avoidance test <strong>and</strong><br />
25
Y maze test. Mice treated with oleamide be<strong>for</strong>e scopolamine injections were<br />
protected from <strong>the</strong> effects.<br />
2.4.5 Antifertility/contraception<br />
The ethyl acetate extract of Z. jujuba bark was found to effect antisteroidogenic<br />
activity <strong>and</strong> hence fertility in adult female mice. It was found to<br />
arrest <strong>the</strong> normal oestrus cycle of adult female mice at diestrus stage <strong>and</strong><br />
reduced <strong>the</strong> wet weight of ovaries significantly. Haematological profiles,<br />
biochemical estimations of whole blood <strong>and</strong> serum remained unaltered in<br />
extract-treated mice. Normal oestrus cycle <strong>and</strong> ovarian steroidogenisis were<br />
restored after withdrawal of treatment. Antifertility activities of crude extracts<br />
were found to be reversible (Gupta et al., 2004).<br />
2.4.6 Hypotensive <strong>and</strong> antinephritic effect<br />
Ziziphus jujuba has been found to stimulate nitric oxide release in vitro, in<br />
cultured endo<strong>the</strong>lial cells <strong>and</strong> in vivo, in <strong>the</strong> kidney tissues of rats (Kim <strong>and</strong><br />
Han, 1996). Kim <strong>and</strong> Han believed that <strong>the</strong> stimulatory effects of Z. jujuba on<br />
nitric oxide release in <strong>the</strong> kidney may contribute to its hypotensive (reduction<br />
of blood pressure) <strong>and</strong> antinephritic (reduction of inflammation of <strong>the</strong> kidney)<br />
action, possibly by increasing renal blood flow (Kim <strong>and</strong> Han, 1996).<br />
2.4.7 Cardiovascular activity<br />
A neo-lignan isolated from Z. mauritiana leaves was found to increase <strong>the</strong><br />
release of endogenous prostagl<strong>and</strong>in I2 (<strong>the</strong> most potent natural inhibitor of<br />
platelet aggregation yet discovered <strong>and</strong> a powerful vasodilator) from <strong>the</strong> rat<br />
aorta by up to 25.3 % at 3 micro g/ml (Fukuyama et al., 1986).<br />
2.4.8 Immunostimulant effects<br />
The leaf extract of Z. jujuba was found to stimulate chemotactic, phagocytic<br />
<strong>and</strong> intracellular killing potency of human neutrophils (infection fighting white<br />
blood cells) at 5-50 micro g/ml (Ganachari et al., 2004).<br />
2.4.9 Antifungal activity<br />
Z. jujuba has been found to show antifungal effects. Ethanol extract from <strong>the</strong><br />
root showed significant inhibitory activity on <strong>the</strong> fungi C<strong>and</strong>ida albicans, C.<br />
tropicalis, Aspergillus flavus, A. niger <strong>and</strong> Malassezia furfur (strains 1374 <strong>and</strong><br />
1765), (Sarfaraz et al., 2002; Mukhtar et al., 2003, 2004).<br />
26
2.4.10 Antidiabetic<br />
Extract of Z. mauritiana was found to have anti-diabetic activity in Wistar rats<br />
(Cisse et al., 2000).<br />
2.4.11 Antiallergic<br />
The anti-allergic activity of aqueous extracts of Z. jujuba was studied by<br />
measuring its inhibitory effect on hyaluronidase (bovine testes) activation in<br />
vitro. Z. jujuba was shown to have strong anti-allergic activity (Su et al., 2000).<br />
2.4.12 Antiulcer activity<br />
The results suggest that Z. mauritiana leaf extracts (ZJE) possesses significant<br />
<strong>and</strong> dose-dependent antiulcer activity. The antiulcer activity of ZJE can be<br />
attributed to its cytoprotective <strong>and</strong> antisecretory action (Ganachari <strong>and</strong> Shiv,<br />
2004).<br />
2.4.13 Antiinflammatory effect<br />
The compound prescription Huangqin Tang which contains <strong>the</strong> fruit of Z.<br />
jujuba showed marked anti-inflammatory effect (Huang et al., 1990). Z.<br />
mauritiana leaf extracts were found to possess significant anti-inflammatory<br />
activity against carrageenan-induced rat paw oedema (Shiv et al., 2004).<br />
2.4.14 Antispastic effect<br />
The compound prescription Huangqin Tang which contains <strong>the</strong> fruit of Z.<br />
jujuba possessed significant antispastic/antispasmodic effect (Huang et al.,<br />
1990).<br />
2.4.15 Antibacterial<br />
An extract of root bark of Z. jujuba exhibited activity against 20 bacteria<br />
(Elmahi et al., 1997). Leaf extracts of Z. mauritiana were found to show<br />
antibacterial effects against Escherichia coli, Klebsiella spp., Pseudomonas<br />
spp., Proteus vulgaris <strong>and</strong> Bacillus subtilis when methanol <strong>and</strong> acetone extract<br />
solvent was used (Chowdary <strong>and</strong> Padashetty, 2000).<br />
2.4.16 Antioxidant effects<br />
Na et al. (2001) found that Z. jujuba extract showed a relatively strong<br />
antioxidative activity.<br />
27
2.5 Summary<br />
Important nutritional properties of jujube fruits relate particularly to <strong>the</strong>ir being<br />
sources of vitamin C, P <strong>and</strong> vitamin B complex in <strong>the</strong> diet.<br />
Although <strong>the</strong>re is a range of potentially useful medicinal substances in jujubes,<br />
<strong>the</strong> research in this area is in its early stages. There is limited interest from<br />
large pharmaceutical companies because many of <strong>the</strong> useful constituents can be<br />
obtained from <strong>o<strong>the</strong>r</strong> botanical sources. The value of such constituents in health<br />
products <strong>and</strong> supplements is undisputed <strong>and</strong> <strong>the</strong> hardy nature of jujubes <strong>and</strong><br />
<strong>the</strong>ir wide geographical range means <strong>the</strong>y can provide a potentially cheap <strong>and</strong><br />
more accessible source of such compounds <strong>for</strong> traditional medicine.<br />
28
Chapter 3. Uses<br />
C. deKock<br />
3.1 Introduction<br />
The fruits of many Ziziphus species are edible <strong>and</strong> are prepared <strong>for</strong><br />
consumption in many ways. They are eaten mostly fresh but may be pickled,<br />
dried <strong>and</strong> made into confectionery, or drinks can be made from <strong>the</strong> juice.<br />
Ziziphus trees are commonly used <strong>for</strong> live fencing, fodder <strong>and</strong> planting to<br />
control soil erosion. The wood also finds a number of local uses.<br />
Leaves can be used as a feed <strong>for</strong> silkworms. Flowers can be <strong>the</strong> source of<br />
nectar <strong>for</strong> honey bees, <strong>and</strong> ber trees are used <strong>for</strong> rearing lac insects.<br />
3.2 Local uses of fruits<br />
3.2.1 South, Sou<strong>the</strong>ast <strong>and</strong> East Asia.<br />
These have been mentioned in Chapter 2 <strong>and</strong> are <strong>the</strong> subject of subsequent<br />
chapters. In addition, people in Sou<strong>the</strong>ast Asia eat unripe fruits with salt<br />
(Morton, 1987).<br />
A wild species, Z. nummularia (Burm.f.) Wight & Arn. (syn. Z. rotundifolia<br />
Lam.) is harvested in western India. Fruits are dried <strong>and</strong> powdered with spices<br />
to prepare a product called ‘churan’ (Pareek, 1983). St<strong>and</strong>ardised products have<br />
not been developed.<br />
A wild species Z. oxyphylla Edgew. (syn. Z. rotundifolia DC) is ga<strong>the</strong>red in<br />
Pakistan <strong>and</strong> used as a subsistence food (Saqib <strong>and</strong> Sultan, 1994).<br />
3.2.2 Africa<br />
In <strong>the</strong> Zambezi valley in Zimbabwe, Ziziphus fruits are eaten fresh from June –<br />
September <strong>and</strong> after dehydration throughout <strong>the</strong> year (Funkhouser, 1998). The<br />
dry powder is used in baking <strong>and</strong> to prepare jam (Maposa <strong>and</strong> Chisuro, 1998)<br />
<strong>and</strong> a traditional loaf (Kadzere, 1998), <strong>and</strong> kachaso, a crude spirit (Arndt,<br />
2001). An alcoholic drink is also made in Malawi (FACT Net).<br />
In West Africa wild Z. mauritiana fruits are used to produce an alcoholic drink.<br />
Z. abyssinica Hochst., a widespread wild African species is locally cultivated<br />
<strong>for</strong> <strong>the</strong> fruits in sou<strong>the</strong>rn Nigeria. Fruits of Z. spina-christi are ga<strong>the</strong>red <strong>for</strong> use<br />
in many parts of West Africa (Hutchinson <strong>and</strong> Dalziel, 1958).<br />
29
Cakes are made out of dried <strong>and</strong> fermented pulp in western Sudan (Dalziel,<br />
1937), <strong>and</strong> in Zambia (Kalikiti, 1998). The Touareg nomads in Mali make flat<br />
bread from dry fruit pulp (Chevalier, 1947) using wild species. In Niger ber<br />
fruits are dried <strong>and</strong> pounded into flour as a famine food (Williams, 1998).<br />
In Egypt nomads, especially <strong>the</strong> Allagi, consume fruits of Z. spina-christi<br />
(Belal et al., 1998). In North Africa Z. lotus (indigenous) <strong>and</strong> Z. jujuba<br />
(introduced) are used <strong>for</strong> fruits.<br />
In Namibia, wild Z. mucronata Willd, is used <strong>for</strong> making a hot liquor, <strong>and</strong><br />
although illegal, provides a source of income <strong>for</strong> <strong>the</strong> rural poor (Hailwa, 1998).<br />
3.2.3 Southwest Asia<br />
Fruits of Z. spina-christi are ga<strong>the</strong>red <strong>and</strong> eaten in many parts of Southwest<br />
Asia e.g. Yemen, Jordan, Oman, Bahrain <strong>and</strong> Saudi Arabia (Non-Wood News;<br />
Arndt, 2001). Cultivation is practised in many parts, <strong>for</strong> example, in Shabwah<br />
Governate of Yemen, households keep an average of 25-50 trees in <strong>and</strong> around<br />
<strong>the</strong>ir irrigated fields <strong>for</strong> bee keeping, fruit production <strong>and</strong> <strong>o<strong>the</strong>r</strong> uses (KIT,<br />
2002).<br />
Sun-dried fruits are powdered <strong>and</strong> mixed with water to make cakes similar to<br />
gingerbread.<br />
3.2.4 South America<br />
Introduced Z. jujuba fruits are used to make a liqueur called ‘crema de<br />
ponsigue’ (Morton, 1987).<br />
Of <strong>the</strong> 7 species of Ziziphus indigenous to <strong>the</strong> New World, Z. mistol Grisels<br />
was found in <strong>the</strong> Andes of Argentina <strong>and</strong> Paraguay to be used <strong>for</strong> making<br />
‘mistol jam’. On <strong>the</strong> whole <strong>the</strong> New World species are not of economic<br />
potential.<br />
3.3 Fodder<br />
Nearly every part of Ziziphus plants can be utilised. The leaves <strong>and</strong> twigs of<br />
most species can be used as nutritious fodder <strong>for</strong> livestock. Due to <strong>the</strong> high dry<br />
weight protein content, leaves are an important source of protein <strong>for</strong> animals<br />
(Arndt, 2001; Dalziel, 1937; Dastur, 1952; Ngwa et al., 2000). Leaves of Z.<br />
mauritiana <strong>and</strong> Z. jujuba are readily eaten by camels, sheep, goats <strong>and</strong> cattle<br />
(<strong>for</strong> goats see Tewatia <strong>and</strong> Khirwar, 2002).<br />
30
In <strong>the</strong> Red Sea area pastoralists with camels that are intended <strong>for</strong> race<br />
competitions <strong>and</strong> that require a special diet utilise <strong>the</strong> winter range of <strong>the</strong> Red<br />
Sea to collect fruits <strong>and</strong> pods of local Ziziphus species.<br />
Collected pods are also fed to lactating <strong>and</strong> pregnant female camels or <strong>the</strong><br />
principal riding camel. The remainder of <strong>the</strong> herd is allowed to browse <strong>for</strong><br />
several days (Organisation <strong>for</strong> Social Science Research in Eastern <strong>and</strong> Sou<strong>the</strong>rn<br />
Africa).<br />
Species of Ziziphus are also browsed by many wild animals.<br />
3.4 Environmental<br />
Ziziphus species can contribute to controlling <strong>the</strong> rate of desertification. Soil<br />
erosion in desert areas is largely due to <strong>the</strong> removal of structureless topsoil by<br />
wind <strong>and</strong> rain. This can largely be checked by planting wind breaks, creating<br />
shelter belts <strong>and</strong> stabilising s<strong>and</strong>y tracts <strong>and</strong> dunes with adapted grasses <strong>and</strong><br />
shrubs like Ziziphus (Khoshoo <strong>and</strong> Subrahmanyam, 1985). Ziziphus<br />
nummularia shrubs have been shown to effectively check wind erosion, help in<br />
deposition of soil, <strong>and</strong> bring about a change in <strong>the</strong> microhabitat, causing<br />
favourable conditions <strong>for</strong> <strong>the</strong> appearance of successional species such as<br />
perennial grasses. In <strong>the</strong> Sahelian climate, Z. mauritiana plays an important<br />
part in <strong>the</strong> conservation of soil because of its abundant <strong>and</strong> vigorous root<br />
systems (Depommier 1988, Arndt 2001). Several species of Ziziphus can<br />
endure extreme stress caused by drought, salinity, <strong>and</strong> in some cases<br />
waterlogging. This makes <strong>the</strong> cultivated jujubes ideal <strong>for</strong> planting on marginal<br />
or degraded l<strong>and</strong>s provided <strong>the</strong> right genotypes are selected <strong>for</strong> alkali-sodic<br />
soils (Dagar et al., 2001) <strong>and</strong> (Hebbara et al., 2002).<br />
3.5 Fuelwood<br />
Z. mauritiana is an excellent fuelwood tree <strong>and</strong> makes a good charcoal, with a<br />
heat content of 4900 kcal kg -1 (Khoshoo <strong>and</strong> Subrahmanyam, 1985). In <strong>the</strong><br />
Sahel zone, it is considered good both as firewood <strong>and</strong> charcoal (Depommier,<br />
1988). Z. nummularia has been reported to produce high-quality hardwood<br />
with high calorific value, making it an ideal source of fuel <strong>and</strong> charcoal (Arndt<br />
2001)<br />
A six year old tree of ber produces an above ground biomass of 11.6 kg in <strong>the</strong><br />
arid northwest India (Toky <strong>and</strong> Bisht, 1993) <strong>and</strong> 8-10 kg air dried fuelwood<br />
from annual prunings (Vashishtha, 1997). Reddy (1988) reported that,<br />
depending upon pruning severity, <strong>the</strong> weight of air-dry pruned wood was 4-6<br />
tons per hectare from 8 year old ber trees in Bangalore, India. According to<br />
Bajwa et al. (1986) <strong>the</strong> weight of prunings per tree ranged from 19.5 to 37.4 kg<br />
from a 13 year old tree. Air-dry biomass of 2 kg/plant was produced two years<br />
31
after planting under rainfed conditions at Dagarkotly in Pakistan (Shah <strong>and</strong><br />
Noor, 1994). The fuelwood yield from pruned wood varies from 1-5 tons per<br />
hectare depending upon spacing, pruning severity <strong>and</strong> agroclimatic conditions.<br />
3.6 Lac culture<br />
<strong>Ber</strong> trees are considered amongst <strong>the</strong> best <strong>for</strong> rearing lac insects (Hussain <strong>and</strong><br />
Khan, 1962; Anon., 1996). A lac yield of 1.5 kg per tree per year was obtained<br />
by collection during October-November at Ranchi in India (Anon., 1996). <strong>Ber</strong><br />
is a chief host plant of Kerria lacca <strong>and</strong> K. sindica (Li <strong>and</strong> Hu, 1994). By using<br />
6-8, 2-3 m long shoots of 2-3 cm thickness on a stump <strong>for</strong> inoculation by lac<br />
insects, a yield of 3-6 kg raw lac can be obtained in 3 years. When used <strong>for</strong><br />
rearing lac insects, use of <strong>the</strong> trees <strong>for</strong> fruits is not viable.<br />
Recent surveys collected socio-economic data from Jharkhan, West Bengal <strong>and</strong><br />
Orissa on lac production (Jaiswal et al., 2002).<br />
3.7 Wood<br />
The wood of Z. mauritiana <strong>and</strong> Z. jujuba is reddish, close-grained, finetextured,<br />
hard, tough, durable <strong>and</strong> planes <strong>and</strong> polishes well. It has been used to<br />
line wells, to make legs <strong>for</strong> bedsteads, boat ribs, agricultural implements, home<br />
poles, tool h<strong>and</strong>les, yokes, gunstocks, saddle trees, s<strong>and</strong>als, golf clubs,<br />
household utensils, toys <strong>and</strong> general craft work.<br />
In India <strong>the</strong> wild type of ber is used <strong>for</strong> many of <strong>the</strong> above purposes (Pearson<br />
<strong>and</strong> Brown, 1932).<br />
The wood does not have value as a commercial timber.<br />
3.8 Bees <strong>and</strong> silkworms<br />
In <strong>the</strong> Islamabad area of Pakistan, Z. jujuba flowers attract honey bees which<br />
can contribute to conservation <strong>and</strong> <strong>the</strong> economic stability of <strong>the</strong> people in <strong>the</strong><br />
local area (Chemas <strong>and</strong> Gray, 1991; Fatima <strong>and</strong> Ramanujam, 1989; Muzaffar,<br />
1998). In India <strong>and</strong> Queensl<strong>and</strong>, <strong>the</strong> flowers of Z. mauritiana <strong>and</strong> Z. jujuba are<br />
rated as a minor source of nectar <strong>for</strong> honeybees (Dash et al. 1992). The honey<br />
is light <strong>and</strong> of fair flavour (Morton, 1987).<br />
In Assam, Ziziphus leaves have been used as a food <strong>for</strong> silkworms. Ziziphus<br />
jujuba has been recorded as a secondary food plant <strong>for</strong> rearing Indian tasar<br />
silkworm, An<strong>the</strong>raea mylitta Drury, larvae <strong>and</strong> proved to be better than <strong>the</strong><br />
primary food plant Shorea robusta (Dash et al. 1992).<br />
32
In China Z. jujuba is a major source of honey. Some is exported as Zao hua<br />
fengmi or ‘jujube-flower honey’ (Wang et al. 1996).<br />
3.9 Medicinal uses<br />
Chapter 2 has already provided in<strong>for</strong>mation on constituents of various parts of<br />
Ziziphus species <strong>and</strong> <strong>the</strong>ir applications. However, <strong>the</strong>re are a large number of<br />
traditional medicinal uses that are not necessarily based on knowledge of <strong>the</strong><br />
constituents. Those that are widespread <strong>and</strong> used consistently are outlined<br />
below.<br />
3.9.1 South Asia<br />
According to Ayurveda, <strong>the</strong> root of Z. nummularia is bitter <strong>and</strong> cooling, <strong>and</strong><br />
cures coughs, biliousness <strong>and</strong> headache. The bark cures boils <strong>and</strong> is good <strong>for</strong><br />
<strong>the</strong> treatment of dysentery <strong>and</strong> diarrhoea. The leaves are antipyretic <strong>and</strong> reduce<br />
obesity. The fruit is cooling, digestible, tonic, aphrodisiac, laxative <strong>and</strong><br />
removes biliousness, burning sensations, thirst, vomiting <strong>and</strong> is also good in<br />
treating tuberculosis <strong>and</strong> blood diseases. The seeds cure eye diseases <strong>and</strong> are<br />
also useful in leucorrhoea (Oudhia, 2001-3).<br />
The traditional workers of Chhattisgarh, India use fresh Z. nummularia fruit to<br />
treat common fevers. The traditional healers of Bastar region use <strong>the</strong> dried<br />
leaves to dress wounds. The fresh leaves are also used <strong>for</strong> <strong>the</strong> same purpose.<br />
The aqueous paste of <strong>the</strong> leaves is applied externally to relieve a burning<br />
sensation. In cases of vomiting, <strong>the</strong> people of Chhattisgarh use <strong>the</strong> seeds with<br />
bar sprouts (Ficus benghalensis) <strong>and</strong> sugar. Roots are used to treat dysentery;<br />
<strong>the</strong>y are given with cow’s milk until <strong>the</strong> patient is cured. Senior citizens used to<br />
use <strong>the</strong> fresh leaf juice of Z. nummularia with buffalo's milk to reduce <strong>the</strong><br />
intensity of smallpox. Similarly, in <strong>the</strong> early days, <strong>the</strong> use of seeds to treat eye<br />
troubles was common. To treat hoarseness of <strong>the</strong> throat, traditional healers<br />
advise patients to keep <strong>the</strong> fresh roots of Z. nummularia inside <strong>the</strong>ir mouth. The<br />
traditional healers of Mudpar village use <strong>the</strong> fresh leaves of Z. nummularia<br />
with cumin to treat urinary infections (Oudhia, 2001-3).<br />
According to <strong>the</strong> Unani system of medicine, <strong>the</strong> roots <strong>and</strong> bark of Z.<br />
nummularia are a tonic, whereas <strong>the</strong> leaves are an<strong>the</strong>lmintic, <strong>and</strong> are good <strong>for</strong><br />
stomatitis <strong>and</strong> gum bleeding. The flowers af<strong>for</strong>d a good collyrium <strong>for</strong> eye<br />
diseases, <strong>the</strong> fruits are sweet <strong>and</strong> sour, <strong>and</strong> can cause diarrhoea in large doses.<br />
The seeds are astringent, are a tonic to <strong>the</strong> heart <strong>and</strong> brain <strong>and</strong> relieve thirst<br />
(Oudhia, 2001-3).<br />
33
3.9.2 Chinese medicine<br />
The Chinese Materia Medica: Chemistry, Pharmacology <strong>and</strong> Applications<br />
describes Z. spinosa, <strong>the</strong> wild spiny Z. jujuba, as having sedative <strong>and</strong> hypnotic<br />
effects in many animal species including humans. In traditional uses it helps to<br />
nourish <strong>the</strong> heart, calm <strong>the</strong> nerves <strong>and</strong> is useful <strong>for</strong> insomnia <strong>and</strong> dream<br />
disturbed sleep (Zhu, 1998).<br />
The wild plant is called suan-tsao. The Chinese have found that <strong>the</strong> wild Z.<br />
jujuba fruit improves <strong>the</strong> health of <strong>the</strong> body. In fact, <strong>the</strong> common belief is that<br />
if <strong>the</strong> fruit is taken on a daily basis, it will improve skin colour <strong>and</strong> tone, both<br />
signs of physical well being (Plant Botanic).<br />
Its domestic counterpart, known as pei-tsao in nor<strong>the</strong>rn China <strong>and</strong> nan-tsao in<br />
<strong>the</strong> south, is considered to be cooling to <strong>the</strong> body. Like an Asian version of <strong>the</strong><br />
aspirin, <strong>the</strong> fruits somehow reduce pain <strong>and</strong> distress. They are strongly<br />
recommended <strong>for</strong> cases of sleeplessness caused from mental fatigue, physical<br />
weakness, or pain. They are used to treat rheumatic symptoms <strong>and</strong> are said to<br />
rejuvenate <strong>the</strong> body, whe<strong>the</strong>r it is suffering from stress or age. The plant is used<br />
to prevent intestinal or respiratory flu <strong>and</strong> to speed <strong>the</strong> recovery process along.<br />
Fresh Z. jujuba is also used to increase strength of <strong>the</strong> seriously ill <strong>and</strong> reverse<br />
<strong>the</strong> process of disease (Plant Botanic).<br />
In modern Chinese medicine, Z. jujuba is used to tone <strong>the</strong> spleen <strong>and</strong> stomach,<br />
to treat shortness of breath <strong>and</strong> severe emotional upset <strong>and</strong> debility due to<br />
nerves, <strong>and</strong> to mask <strong>the</strong> flavours of unpleasant-tasting herbs (Plant Botanic).<br />
Z. jujuba pips, when aged <strong>for</strong> three years, are considered excellent <strong>for</strong> wounds<br />
<strong>and</strong> abdominal pain. The leaves are used to treat children suffering from<br />
typhoid fever. They induce sweating which is thought to break <strong>the</strong> fever. They<br />
are also used <strong>for</strong> a number of infectious diseases. The heartwood is considered<br />
a powerful blood tonic. The root is used to promote hair growth <strong>and</strong> in treating<br />
fevers in children such as smallpox, measles, <strong>and</strong> chicken pox. The bark is used<br />
to make an eye wash <strong>for</strong> inflamed eyes (Plant Botanic).<br />
3.9.3 O<strong>the</strong>r areas<br />
The Arabs use <strong>the</strong> fruits of Z. jujuba, Z. mauritiana <strong>and</strong> Z. spina-christi to<br />
ensure health. The leaves of <strong>the</strong> plant kill diarrhoea-causing parasites <strong>and</strong><br />
worms in <strong>the</strong> intestinal tract. The fruits are said to cure coughs, resolve any<br />
<strong>o<strong>the</strong>r</strong> lung complaints, soo<strong>the</strong> <strong>the</strong> internal organs <strong>and</strong> reduce water retention.<br />
In Saudi Arabia, fruits of Z. spina-christi when in sufficient strength act as a<br />
laxative. Stem bark is used to relieve toothache <strong>and</strong> fevers (Al-Khalifa <strong>and</strong><br />
Sharkas, 1984; Al-Akeely, 1985). Leaves of Z. spina-christi are used in<br />
traditional medicine in Egypt <strong>for</strong> <strong>the</strong> treatment of abscesses, boils <strong>and</strong> swollen<br />
34
eyes <strong>and</strong> its wood ash <strong>for</strong> <strong>the</strong> treatment of snakebite (Abdul-Galil <strong>and</strong> El-<br />
Jissary, 1991). The root, stem bark <strong>and</strong> leaves are used in various medicinal<br />
preparations in tropical Africa, particularly in <strong>the</strong> Kapisiki country (Dalziel,<br />
1937; Heyne, 1950; Williamson, 1957; Depommier, 1988).<br />
In Zimbabwe, Z. mucronata roots are a commonly used part of <strong>the</strong> plant <strong>for</strong><br />
urinary <strong>and</strong> gynaecological complaints, but traditional practices vary from<br />
region to region; bark decoctions have been recorded in South Africa <strong>for</strong> chest<br />
diseases (Tree Society of Zimbabwe, 2001).<br />
In Haiti, fruits, leaves <strong>and</strong> roots of introduced Z. jujuba are boiled to make a<br />
decoction <strong>and</strong> this is used as tea <strong>for</strong> an antidote to poison (Plant Botanic).<br />
Z. juazeiro is used in Brazilian herbal medicine. However, this species is not<br />
discussed in this <strong>monograph</strong>: <strong>for</strong> fur<strong>the</strong>r in<strong>for</strong>mation see Raintree Nutrition.<br />
35
Chapter 4. Climate <strong>and</strong> Ecology<br />
4.1 Introduction<br />
(Revised by J.T. Williams)<br />
Most species of Ziziphus can be found in low rainfall areas. The climatic <strong>and</strong><br />
ecological background to <strong>the</strong> three important cultivated species is shown in<br />
Table 4.1.<br />
Table 4.1 Ecological background of three Ziziphus species<br />
Z. mauritiana Z. jujuba Z. spina-christi<br />
Latitude 30 o N to 30 o S 30 o S to 51 o N 0 o to 20 o N<br />
Altitude m < 1500 Up to 2800 < 1000<br />
Eco-region Warm lowl<strong>and</strong><br />
plains<br />
Cool highl<strong>and</strong>s Mediterranean<br />
dryl<strong>and</strong>s<br />
Minimum 4 o to 12 o C -10 o to -20 o C -5 to 2 o C<br />
temperature<br />
Maximum 39 o to 45 o C 36 o C ±5 o C<br />
temperature<br />
Rainfall > 300 mm 200 to 450 mm ca. 100 mm<br />
Soil type Shallow to deep<br />
aridisols<br />
Alluvial plains<br />
<strong>and</strong> hills<br />
Poor soils of arid<br />
areas<br />
Soil salinity Neutral to slightly Highly tolerant Medium tolerance<br />
alkaline (5 dSm -i )<br />
Alkalinity < 45 ESP Highly tolerant Some tolerance<br />
This background explains <strong>the</strong> extremely wide distribution of wild <strong>and</strong><br />
cultivated <strong>for</strong>ms of <strong>the</strong> species. In<strong>for</strong>mation given below is mostly taken from<br />
(Pareek, 2001).<br />
4.2 Temperature<br />
4.2.1 <strong>Ber</strong><br />
<strong>Ber</strong> grows well under varying climatic conditions from sea level up to an<br />
elevation of 1000 m (Singh et al., 1973 a) although it produces best below 600<br />
m; it can be grown to altitudes up to 1500 m. Commercial ber plantations are<br />
found growing in areas having a minimum temperature of 4 to 12 C <strong>and</strong><br />
occasionally reaching as low as -2 C <strong>for</strong> short periods, although this can injure<br />
36
young shoots <strong>and</strong> fruits. Freezing temperatures <strong>and</strong> frost, however, cause<br />
damage to young twigs <strong>and</strong> developing fruits <strong>and</strong> result in considerable crop<br />
loss <strong>and</strong> decline in tree growth.<br />
Pareek (1983) outlined <strong>the</strong> temperature dependency <strong>for</strong> time of growth,<br />
flowering <strong>and</strong> fruit maturity. <strong>Ber</strong> trees can withst<strong>and</strong> extremely high summer<br />
temperatures <strong>and</strong> are found to grow well in regions having maximum<br />
temperatures of 39 to 42 C, <strong>and</strong> can tolerate temperatures as high as 49-50 C.<br />
However, fruit set is adversely affected at temperatures above 35 C. The trees<br />
shed leaves <strong>and</strong> enter dormancy during <strong>the</strong> extremely hot summers in <strong>the</strong><br />
subtropics of nor<strong>the</strong>rn India. In nor<strong>the</strong>rn Australia, leaf senescence <strong>and</strong> leaf fall<br />
begins in April as <strong>the</strong> dry season sets in, <strong>and</strong> <strong>the</strong> new leaves emerge with <strong>the</strong><br />
onset of rainfall in September <strong>and</strong> October (Grice, 1998). This appears to be an<br />
adaptive mechanism to escape damage through desiccation during hot wea<strong>the</strong>r.<br />
Desiccation damage in ber is caused by high cuticular transpiration, which is<br />
reported to be associated with high levels of fatty acids <strong>and</strong> low levels of<br />
aldehydes <strong>and</strong> alcohols in <strong>the</strong> wax cuticle ra<strong>the</strong>r than with <strong>the</strong> thickness of <strong>the</strong><br />
cuticle <strong>and</strong> wax itself (Rao et al., 1981). During <strong>the</strong> dormancy phase, along<br />
with leaf fall, growth ceases. Dark tan-coloured hard <strong>and</strong> pubescent scales<br />
develop on <strong>the</strong> buds <strong>and</strong> <strong>the</strong> bark <strong>and</strong> buds lose moisture <strong>and</strong> show lower<br />
nitrogen contents (Singh et al., 1974 b).<br />
In regions with less extreme temperatures, summer dormancy ei<strong>the</strong>r does not<br />
occur or is very brief, resulting in almost no check in growth. Thus growth,<br />
flowering <strong>and</strong> development all vary depending upon prevailing temperature<br />
conditions.<br />
4.2.2 Chinese jujube<br />
Chinese jujube grows well at average temperatures of 20-28 C in areas having<br />
a frost-free period of 100-180 days a year <strong>and</strong> can tolerate winter temperatures<br />
of -10 to -20 C (Ming <strong>and</strong> Sun, 1986). Fruits mature 2 weeks earlier in <strong>the</strong><br />
warmer areas of Azerbaijan where summer temperature rises to 36 C (Tagiev,<br />
1992). In <strong>the</strong> USA, Chinese jujube has withstood temperatures of -22 C<br />
without injury (Thomas, 1924) <strong>and</strong> has tolerated -30 C in Azerbaijan (Troyan<br />
<strong>and</strong> Kruglyakov, 1972).<br />
Tolerance to low temperatures seems to be due to cultivar differences<br />
(Kucherova <strong>and</strong> Sin’ko, 1984 b; Sin’ko et al., 1987; Ivanova et al., 1989). Wild<br />
<strong>for</strong>ms of Chinese jujube are also resistant to low temperatures.<br />
Cultivars can be evaluated <strong>for</strong> frost tolerance on <strong>the</strong> basis of resistance to<br />
dehydration. Water retaining capacity in shoots of different cultivars varies.<br />
The cultivars having high water retaining capacity are capable of tolerating<br />
drying spring winds which retard bud break in Chinese jujube growing in <strong>the</strong><br />
steppe region of Crimea (Kucherova <strong>and</strong> Sin’ko, 1989).<br />
37
Chinese jujube remains in <strong>the</strong> dormant stage from <strong>the</strong> middle of October<br />
through <strong>the</strong> winter until <strong>the</strong> end of January (Kim et al., 1982 a). During this<br />
period, <strong>the</strong> total carbohydrate content (reducing <strong>and</strong> non reducing sugars)<br />
decreases steadily but starts increasing again from March. The peak activity of<br />
-amylase <strong>and</strong> invertase was observed in November, that of -amylase, acid<br />
phosphatase <strong>and</strong> alkaline phosphatase in January <strong>and</strong> protease activity<br />
increased from January to April.<br />
4.3 Rainfall<br />
4.3.1 <strong>Ber</strong><br />
Natural groves of ber grow <strong>and</strong> produce well in subtropical <strong>and</strong> tropical regions<br />
receiving over 400 mm annual rainfall. Fruit yields are higher during higher<br />
rainfall years (Singh et al., 1998). Management of trees in low rainfall areas<br />
necessitates some irrigation. Conditions of high atmospheric vapour pressure<br />
deficit result in <strong>the</strong> production of better quality (sweet <strong>and</strong> large sized) fruits<br />
than in humid areas. The incidence of pests <strong>and</strong> diseases is also lower in drier<br />
regions. <strong>Ber</strong> exhibits drought tolerance by osmotic adjustment <strong>and</strong> <strong>the</strong> deep tap<br />
root (Arndt et al., 2000). Species used as rootstocks (see Chapter 5) tend to be<br />
those occurring in areas receiving low rainfall. <strong>Ber</strong> can, depending on <strong>the</strong><br />
cultivar, withst<strong>and</strong> slightly waterlogged conditions.<br />
4.3.2 Chinese jujube<br />
Chinese jujube plantations are common in north-west China, including arid<br />
areas with annual rainfall below 200 mm, semi-arid areas with 200 to 450 mm<br />
rainfall <strong>and</strong> sub-humid areas with 450 to 650 mm rainfall (Ming <strong>and</strong> Sun,<br />
1986). Chinese jujube is reported to withst<strong>and</strong> severe drought (Lanham, 1926;<br />
Locke, 1948; Sin’ko, 1971) because its vertical root system reaches a depth of<br />
13 m (Ming <strong>and</strong> Sun, 1986).<br />
4.4 Soils<br />
4.4.1 <strong>Ber</strong><br />
<strong>Ber</strong> grows on a wide range of soils from gravelly, shallow soils to deep<br />
aridisols <strong>and</strong> to some extent on entisols (Pareek, 1983). Even in soils underlain<br />
with murram (calcic subhorizon) within one metre depth, roots were found to<br />
penetrate up to 4.5 m (Pareek, 1977). Data from field trials in India <strong>and</strong><br />
Zimbabwe suggest that in Ziziphus rooting depth is critical <strong>for</strong> <strong>the</strong> maintenance<br />
of high rates of assimilation <strong>and</strong> conductance throughout <strong>the</strong> day making it<br />
tolerant to drought conditions (Clif<strong>for</strong>d et al., 1996).<br />
38
4.4.2 Chinese jujube<br />
Chinese jujube also grows on a variety of soils. In <strong>the</strong> Yeongnam region of<br />
Korea, 42 % of Chinese jujube plantations are on alluvial plains, 23 % on<br />
mountain foothills, 22 % in valleys <strong>and</strong> 13 % on hills (Kim et al., 1989). Fruit<br />
yields are higher on alluvial soils <strong>and</strong> on gently sloping fans than on <strong>the</strong> hill<br />
l<strong>and</strong>s <strong>and</strong> steeper slopes where <strong>the</strong> soils are shallow. In Azerbaijan, jujube<br />
plantations have been established on s<strong>and</strong>y as well as clay soils (Tagiev, 1992).<br />
4.4.3 Stress conditions<br />
Both major cultivated species are tolerant to a degree of salinity; ber up to 6<br />
dSm -1 <strong>and</strong> Chinese jujube higher (Oganesjan, 1953; Dhankhar et al., 1980;<br />
Dahiya et al., 1981; Rao <strong>and</strong> Kh<strong>and</strong>elwal, 2001). Species used <strong>for</strong> rootstocks<br />
<strong>for</strong> ber are also salt tolerant (Meena et al. 2003). In terms of soil fertility, both<br />
species require N <strong>and</strong> P but K has little effect on <strong>the</strong>ir growth (Lal et al., 2003).<br />
Boron inhibits uptake of P <strong>and</strong> K in Chinese jujube (Lee <strong>and</strong> Choi, 1992). <strong>Ber</strong><br />
is of great interest <strong>for</strong> production <strong>and</strong> reclamation of <strong>the</strong> alkali soils of India<br />
(ca. 3.58 million ha) which have high pH, low organic carbon, low fertility,<br />
excessive exchangeable sodium <strong>and</strong> indurated CaCO 3 (Dagar et al., 2001).<br />
<strong>Ber</strong> is known to survive even in soils having pH as high as 9.2 (Jaw<strong>and</strong>a et al.,<br />
1981). No leaf scorching in trees growing on alkaline soils was observed while<br />
those of mango <strong>and</strong> guava were seriously damaged (Samra, 1985). Young ber<br />
seedlings survived when transplanted in soils up to 66 ESP (Exchangeable<br />
Sodium Percentage) in a greenhouse (Singh, et al., 1983 b). Increasing ESP<br />
levels, however, reduced growth, decreased Ca <strong>and</strong> Mn, but increased Na <strong>and</strong><br />
Fe contents in <strong>the</strong> leaves. In pot experiments, seed germination <strong>and</strong> emergence<br />
was reduced in 40 ESP soil <strong>and</strong> a fur<strong>the</strong>r increase in ESP resulted in reduction<br />
in <strong>the</strong> amount of P, K, Ca, Mg, Zn <strong>and</strong> Mn (Patil et al., 1981; Mehta, 1982)<br />
<strong>and</strong> increase in <strong>the</strong> amounts of Na, B <strong>and</strong> Fe in <strong>the</strong> plants (Mehta, 1982).<br />
Kumar et al. (1990) also observed a decrease in leaf micronutrient content with<br />
an increase in ESP levels from 5 to 45.3. The total chlorophyll, free amino acid<br />
<strong>and</strong> proline contents increased with increasing sodicity (P<strong>and</strong>ey et al., 1991).<br />
Awasthi et al. (1994) reported that 62.5 % ber seedlings survived at 60.5 ESP<br />
but none of <strong>the</strong> grafted plants of Umran <strong>and</strong> Gola survived. Shoot <strong>and</strong> root<br />
growth of Umran ber decreased with increasing ESP (Patil et al., 1981).<br />
39
5.1 Introduction<br />
Chapter 5. Propagation<br />
E. Bonkoungou<br />
Wild populations of Ziziphus regenerate naturally by seed, <strong>and</strong> frequently<br />
produce root sprouts. However, collecting <strong>and</strong> germinating seed is <strong>the</strong> way by<br />
which Ziziphus seedlings are raised directly in <strong>the</strong> field or in nurseries <strong>for</strong> a<br />
wide range of purposes.<br />
Reproduction by seed, however, does not guarantee true-to-type reproduction<br />
of <strong>the</strong> desirable traits of <strong>the</strong> m<strong>o<strong>the</strong>r</strong> tree due to cross pollination <strong>and</strong> subsequent<br />
segregation of plant characters in <strong>the</strong> progeny. Hence commercial <strong>and</strong> much<br />
local propagation <strong>for</strong> orchards of improved cultivars is by vegetative means.<br />
Outside its native area, uncontrolled propagation of Ziziphus can lead to serious<br />
weed problems. In Australia, where <strong>the</strong> species was introduced in <strong>the</strong> 1800s <strong>for</strong><br />
horticultural <strong>and</strong> ornamental purposes, it is now declared a noxious weed.<br />
Initially planted around early settlements, it is said to <strong>for</strong>m dense thickets<br />
which seriously hamper livestock management <strong>and</strong> reduce pasture production<br />
<strong>and</strong> accessibility in parts of Queensl<strong>and</strong> (Grice, 1996). Thus, although ber, <strong>and</strong><br />
Chinese jujube, are extremely valuable trees in <strong>the</strong> correct environment, <strong>the</strong>ir<br />
potential to become weeds should not be ignored, particularly in areas where<br />
trees have naturalised (William <strong>and</strong> West, 2000) such as Australia or New<br />
Zeal<strong>and</strong>.<br />
5.2 Seed propagation<br />
5.2.1 Seed characteristics<br />
<strong>Ber</strong> seeds are enclosed within a hard woody endocarp known as <strong>the</strong> stone<br />
which is sometimes wrongly referred to as <strong>the</strong> seed. Each fruit contains one<br />
stone embedded in <strong>the</strong> pulp at <strong>the</strong> centre of <strong>the</strong> fruit. The stone (see Fig 1.2)<br />
can be depulped in many ways: manually by removing <strong>the</strong> pulp, pounding<br />
dried fruits in a mortar, or by running <strong>the</strong> fruits through a macerator with water<br />
<strong>and</strong> floating off <strong>the</strong> pulp. Stones vary in shape from round to subovate to ovate<br />
with more or less pronounced ridges on <strong>the</strong> outer surface (ICUC, 2002).<br />
Cleaned stones are about 1-2 cm in size.<br />
The stone may contain as many as three seeds embedded in <strong>the</strong> endocarp of <strong>the</strong><br />
drupe (Pareek, 2001) but <strong>the</strong> presence of only one <strong>and</strong> two seeds per stone also<br />
has been reported. In Australia, Grice (1996) found that <strong>the</strong> most frequent case<br />
is a single seed per stone <strong>and</strong> occasionally two. ICRAF (1992) reports two to<br />
40
three seeds per stone in Kenya, whereas in Tanzania <strong>the</strong> most frequent number<br />
is two seeds in a large stone (Kuffo et al., 2002; Mbuya et al., 1994). In West<br />
<strong>and</strong> Central Africa, Diallo (2002) reported one to two seeds per stone in a study<br />
conducted on Ziziphus mauritiana provenances from Senegal, <strong>the</strong> Gambia <strong>and</strong><br />
Chad. All <strong>the</strong> Chad provenances had two seeds per stone. In Senegal, 80 % of<br />
<strong>the</strong> stones from fruits collected at Dahra <strong>and</strong> in Dakar had two seeds each<br />
(Danthu et al., 1992).<br />
Ziziphus stones <strong>and</strong> seeds are relatively light in weight. For Z. mauritiana,<br />
Roussel (1995) reported 3,500 to 4,000 stones to <strong>the</strong> kilogram. In Burkina<br />
Faso, Ouedraogo <strong>and</strong> Nikiema (1997) also found 3,500 stones to <strong>the</strong> kilogram.<br />
Von Maydell (1983) reported a wide range from 3,600 to 7,000 stones to <strong>the</strong><br />
kilogram <strong>for</strong> <strong>the</strong> Sahel region <strong>and</strong> explained that <strong>the</strong> wide range was due to<br />
impurities in some of <strong>the</strong> seedlots. In nor<strong>the</strong>rn Cameroon, Depommier (1988)<br />
reports only 350 to 650 stones to <strong>the</strong> kilogram. If confirmed, this would be a<br />
case of unusually heavy seeds (ten times heavier than <strong>the</strong> average weight<br />
commonly reported <strong>for</strong> Z. mauritiana throughout <strong>the</strong> region). For Z.<br />
mucronata, Roussel (1995) found 2,000 to 2,200 stones to <strong>the</strong> kilogram. Thus,<br />
apart from <strong>the</strong> ra<strong>the</strong>r unusual case reported in Cameroon, Z. mucronata seeds<br />
appear to be heavier than those of Z. mauritiana.<br />
5.2.2 Seed viability<br />
Under natural conditions, seeds from fruits that fall <strong>and</strong> lie on <strong>the</strong> soil surface<br />
may remain viable <strong>for</strong> up to 12 months. Data currently available do not suggest<br />
that a large proportion of seeds remain dormant in <strong>the</strong> soil <strong>for</strong> much longer<br />
periods. In Australia, Grice (1996) observed that germination rate in Z.<br />
mauritiana seeds collected from <strong>the</strong> soil surface declined from a rate of 56 % in<br />
<strong>the</strong> control (fresh dehulled seeds) to 31 % after six months, <strong>the</strong>n to 20 % at 12<br />
months. For seeds that remain buried in <strong>the</strong> soil (at 2 cm depth) <strong>the</strong> germination<br />
rate declines sharply to 7 % after six months. In Tamil Nadu, India, Srimathi et<br />
al. (2002) found that cv. Umran seeds from fruits collected from <strong>the</strong> crown<br />
exhibited higher germination rates than those collected from <strong>the</strong> ground.<br />
Storage conditions have an expected significant effect on seed germination. A<br />
review by Pareek (2001) indicated that storage at reduced temperatures of 4.5 +<br />
0.5 º C in per<strong>for</strong>ated poly<strong>the</strong>ne bags result in retention of viability <strong>for</strong> longer<br />
periods. <strong>Ber</strong> seeds can remain viable <strong>for</strong> two <strong>and</strong> half years when kept in a dry<br />
<strong>and</strong> cool environment, but storage time is dependent on <strong>the</strong> condition of <strong>the</strong><br />
seeds <strong>and</strong> how well <strong>the</strong>y have been dried prior to storage (ICUC, 2002). For<br />
long-term storage seeds behave in an orthodox manner <strong>and</strong> can be stored in low<br />
temperatures when dried properly (see Chapter 8 Genetic Resources).<br />
A simple <strong>and</strong> rapid method to test seed viability is to float <strong>the</strong> stones in salt<br />
solution. Seeds that float probably have air pockets caused by insect damage or<br />
dead embryos. Such seeds should be discarded. Seeds that sink are viable.<br />
41
Srimathi et al. (2002) soaked dried stones of ber cv. Umran in 15, 18 <strong>and</strong> 20 %<br />
salt solution <strong>and</strong> found that only <strong>the</strong> seeds which sink could be used <strong>for</strong><br />
seedling production in a nursery. The recovery of floaters increased with<br />
increasing salt concentration <strong>and</strong> germination was improved by grading <strong>the</strong><br />
stones using 20 % salt solution.<br />
As indicated by Pareek (2001), <strong>the</strong> viability of seeds can also be assessed by<br />
<strong>the</strong> tetrazolium test. For this test, <strong>the</strong> indicator used is a colourless solution of<br />
triphenyl tetrazolium chloride or bromide (Kamra, 1992). In actively respiring<br />
areas of <strong>the</strong> seed <strong>the</strong> colourless solution reacts with hydrogen ions produced by<br />
<strong>the</strong> dehydrogenase enzyme <strong>and</strong> turns into a red, stable <strong>and</strong> non diffusible<br />
substance. This makes it possible to distinguish <strong>the</strong> red coloured living parts of<br />
seeds from <strong>the</strong> colourless dead ones. However, this test is time consuming; also<br />
interpretation of results may be difficult.<br />
5.2.3 Seed germination<br />
Seed germination is affected by <strong>the</strong> initial percentage viability at <strong>the</strong> time of<br />
seed collection, <strong>and</strong> by storage conditions, environmental conditions at sowing<br />
time, <strong>and</strong> treatments applied to break dormancy.<br />
The degree of fruit ripeness has a significant effect on germination of <strong>the</strong><br />
enclosed seed. <strong>Ber</strong> seed germination in Senegal increased from a mere 2 % <strong>for</strong><br />
seeds from green fruits to 28 % when fruits are more mature <strong>and</strong> have turned<br />
yellow <strong>and</strong> 56 % <strong>for</strong> seeds from fully ripe fruits that have turned red. The rate<br />
declines to 46 % <strong>for</strong> seeds from overripe fruits that have turned brown (Danthu<br />
et al., 1992). This has practical implications <strong>for</strong> seed collection as fruit colour<br />
can be used to determine <strong>the</strong> most appropriate time to collect seeds.<br />
Pareek (2001) also noted <strong>the</strong> importance of seed age <strong>for</strong> optimum germination<br />
as ber seeds can germinate only after a period of after-ripening. One or two<br />
months after extraction, germination increases <strong>and</strong> one year old seeds<br />
germinate better than <strong>the</strong> freshly extracted ones. Sowing freshly extracted seeds<br />
gave only 33 % germination which increased after two months, reaching 50 %<br />
after storage <strong>for</strong> eight months. Seedling vigour was also <strong>the</strong> highest when <strong>the</strong><br />
seeds were sown after eight months storage. Seed size (small, medium <strong>and</strong><br />
large) also affects germination. Singh et al. (2004) report greatest ber seed<br />
germination <strong>and</strong> tallest seedlings from medium sized seeds.<br />
5.2.4 Seed pretreatments<br />
Even when <strong>the</strong>y are viable ber seeds do not germinate readily. Suitable<br />
conditions <strong>for</strong> germination must be created. Under natural conditions in <strong>the</strong><br />
field, seed dormancy gradually breaks down as <strong>the</strong> stone wea<strong>the</strong>rs naturally on<br />
<strong>the</strong> ground. For controlled germination, a common nursery practice is to<br />
pretreat seeds if samples take more than a week to germinate. Pretreatment falls<br />
42
into two main categories: mechanical scarification, <strong>and</strong> non mechanical<br />
methods.<br />
Mechanical scarification of ber seeds involves cracking, nicking, or partial<br />
removal of <strong>the</strong> stony endocarp. This appears to be <strong>the</strong> single most efficient<br />
pretreatment to achieve highest percentage of germination. Less than 10 % of<br />
fresh ber seeds will germinate without removal of <strong>the</strong> endocarp (Grice, 1996).<br />
Cracking <strong>the</strong> endocarp can achieve 100 % germination in two weeks (Bill<strong>and</strong><br />
<strong>and</strong> Diallo, 1991). A rate of 85 – 90 % germination over a period of 12 days<br />
with this treatment has been reported by Ouedraogo <strong>and</strong> Nikiema (1997).<br />
Murthy et al. (1989) reported a germination rate of 44.58 % <strong>for</strong> cracked stones<br />
while <strong>the</strong> control of intact stones achieved a mere 17.50 %. Mechanical<br />
scarification of <strong>the</strong> endocarp not only achieves high percentages of<br />
germination; it also speeds up germination. Germination of non scarified stones<br />
is slow <strong>and</strong> may take up to four weeks, whereas extracted seeds germinate<br />
within a week <strong>and</strong> <strong>the</strong> seedlings are more vigorous (ICUC, 2002).<br />
Non mechanical pretreatments involve soaking whole stones or dehulled seeds<br />
in water or in various chemical solutions such as sulphuric acid or a range of<br />
growth regulators. A review by Pareek (2001) indicated that ABA- like<br />
substances are present in <strong>the</strong> testa of <strong>the</strong> seed <strong>and</strong> that germination was reduced<br />
as a result of soaking <strong>the</strong> seeds in 500 ppm abscissic acid solution. Treatment<br />
with 5 ppm abscissic acid inhibits germination of Chinese jujube seeds.<br />
When viable stones are dipped in 500 ppm thiourea <strong>for</strong> four hours <strong>and</strong> <strong>the</strong>n<br />
cracked, <strong>the</strong> separated seeds will germinate in seven days (Morton, 1987) while<br />
seeds in uncracked stones require 21 to 28 days. Vashishtha (1998) reported<br />
that pretreatment of stones in concentrated sulphuric acid <strong>and</strong> GA improved<br />
germination, but soaking in water even <strong>for</strong> 48 hours was not helpful. A<br />
common pretreatment of ber stones in Burkina Faso is to soak <strong>the</strong> stones in<br />
sulphuric acid (97 %) <strong>for</strong> 30 minutes <strong>the</strong>n in water <strong>for</strong> 24 hours. Results of 80 –<br />
100 % germination have been obtained this way (Bill<strong>and</strong> <strong>and</strong> Diallo, 1991;<br />
Ouedraogo <strong>and</strong> Nikiema, 1997).<br />
Passage of stones through <strong>the</strong> digestive tract of animals hastens germination.<br />
The stones can remain in <strong>the</strong> digestive tract <strong>for</strong> at least 12 days. A large<br />
proportion of seeds excreted by cattle contain viable seeds that achieve 88 %<br />
germination (Grice, 1996).<br />
O<strong>the</strong>r non mechanical pretreatments include exposing stones or seeds to<br />
environmental factors such as specific temperature or various growth media. In<br />
germination tests of seeds under four temperature regimes (25, 30, 35 <strong>and</strong> 40º<br />
C) in darkness by Danthu et al. (1992), germination rate after seven days was<br />
90 – 91 % at 35º C, 85 – 87 % at both 30 <strong>and</strong> 25º C, <strong>and</strong> no germination was<br />
observed at 40º C. Although final rates of germination at 25, 30 <strong>and</strong> 35º C are<br />
comparable after seven days, speed of germination is markedly different.<br />
43
Germination after two days was a mere 0 – 10% at 25º C, but reached 80 % <strong>and</strong><br />
more at both 30 <strong>and</strong> 35º C. A review by Pareek (2001) reported similar results.<br />
For Chinese jujube seeds, 25º C proves to be optimum.<br />
Conditions of <strong>the</strong> growing medium have considerable effects on germination.<br />
The available data have been reviewed in detail by Pareek (2001) as follows.<br />
Salinity in <strong>the</strong> growing medium delays or inhibits germination of ber seeds.<br />
Increasing chloride <strong>and</strong> bicarbonate concentration from 2 to 10 dSm –1 in<br />
irrigation waters tended to decrease seed germination with significant reduction<br />
at 4 dSm –1 of chloride waters <strong>and</strong> 7.5 dSm –1 of bicarbonate waters.<br />
Germination declined to 50 % at 6 dSm –1 EC compared to that at 1.5 dSm –1 <strong>and</strong><br />
failed completely at 12 dSm –1 . Increasing soil boron levels from 4 to 16 ppm<br />
has no appreciable effect on final emergence but in combination with salinity<br />
delays <strong>the</strong> germination. Alkalinity at ESP 40 in <strong>the</strong> growing medium also<br />
delayed seed emergence.<br />
Seeds of Chinese jujube sown in <strong>the</strong> open <strong>and</strong> covered with plastic sheeting<br />
emerge 20 days earlier than non covered seeds <strong>and</strong> also gave 22 % higher<br />
emergence.<br />
Dehulled seeds do not appear to require major pretreatments. Danthu et al.<br />
(1992) observed that Z. mauritiana seeds do not require any pretreatment; <strong>the</strong>y<br />
will germinate readily. Prins <strong>and</strong> Maghembe (1994) achieved more than 80 %<br />
germination by simply cleaning <strong>and</strong> soaking <strong>the</strong> seeds in water. Dehulled seeds<br />
soaked in water <strong>for</strong> 24 hours reached 100 % germination in two weeks (Bill<strong>and</strong><br />
<strong>and</strong> Diallo, 1991). In Chinese jujube, a review by Pareek (2001) showed that<br />
one group of cultivars gives 85 % seed germination (e.g. Ya-tszao) <strong>and</strong> <strong>the</strong><br />
<strong>o<strong>the</strong>r</strong> (e.g. Nikitskii 84, 92 <strong>and</strong> 94) gives 98 % germination. Some Chinese<br />
jujube seeds take one to three days to germinate while <strong>o<strong>the</strong>r</strong>s take seven days.<br />
5.2.5 The nursery<br />
5.2.5.1 Seed propagation<br />
<strong>Ber</strong> seedlings raised from seeds are not used directly <strong>for</strong> fruit production in<br />
commercial plantations because <strong>the</strong> time taken <strong>for</strong> such plants to reach bearing<br />
age is usually longer than <strong>for</strong> trees propagated using vegetative methods<br />
(ICUC, 2002). Also <strong>the</strong> desirable traits of improved cultivars (growth, fruiting<br />
<strong>and</strong> fruit quality) are not guaranteed through seed reproduction.<br />
None<strong>the</strong>less, propagation of ber <strong>and</strong> <strong>the</strong> <strong>o<strong>the</strong>r</strong> major jujubes by seed remains of<br />
great value <strong>for</strong> several reasons:<br />
(i) Propagation by seed is necessary to raise appropriate rootstocks <strong>for</strong><br />
vegetative propagation of improved cultivars.<br />
(ii) In regions where jujubes are propagated not solely <strong>for</strong> fruits but also <strong>for</strong> a<br />
44
ange of products <strong>and</strong> services (live hedges, fodder, timber etc.), propagation<br />
by seed is a much easier <strong>and</strong> more economical method than vegetative<br />
propagation. Until <strong>the</strong> recent introduction of improved cultivars to <strong>the</strong> Sahel<br />
region of West Africa, most research <strong>and</strong> development programmes on Z.<br />
mauritiana in <strong>the</strong> region focused on per<strong>for</strong>mance in live hedge technology in<br />
agro<strong>for</strong>estry systems under rainfed conditions. This requires large scale<br />
production of seedlings sown directly in <strong>the</strong> field or raised in private <strong>and</strong><br />
community nurseries in villages throughout <strong>the</strong> region. In such situations,<br />
propagation by seed is <strong>the</strong> safest way to produce seedlings with deep tap roots<br />
that can survive in <strong>the</strong> field under extended moisture stress even when <strong>the</strong><br />
surface soil completely dries out.<br />
(iii) Sexual reproduction by seed offers opportunities <strong>for</strong> variation <strong>and</strong><br />
evolutionary advancement, which is of immense value to <strong>the</strong> plant breeder.<br />
(iv) Conservation of Ziziphus biodiversity <strong>and</strong> rehabilitation of natural<br />
vegetation is best served through seed reproduction.<br />
5.2.5.2 Techniques <strong>for</strong> raising seedlings<br />
Seedlings may be raised in nurseries by sowing seeds in seedbeds or in<br />
containers. Quality seedlings in <strong>the</strong> nursery are fundamental to quality trees in<br />
<strong>the</strong> field. As Jaenicke (1999) pointed out, <strong>the</strong> best looking seedling in <strong>the</strong><br />
nursery is worthless if it does not survive <strong>and</strong> grow after planting out (see<br />
Plates 1.2).<br />
For ber, seeds should be sown at a depth of 2 cm at 30 x 30 cm spacing in <strong>the</strong><br />
seedbed any time from spring through <strong>the</strong> monsoon period (Pareek, 2001). For<br />
transplanting in <strong>the</strong> field, nursery bed raised seedlings have to be lifted, packed<br />
<strong>and</strong> transported to <strong>the</strong> planting site. Seedlings can be transplanted in <strong>the</strong> field<br />
with 20 x 15 cm earth ball; <strong>the</strong>y can also be transplanted bare rooted (without<br />
ball) when <strong>the</strong>y are not growing actively during <strong>the</strong> winter in subtropical<br />
climates (Pareek, 2001). Bed raised seedlings often suffer high mortalities<br />
during transplanting because of root injuries when seedlings are lifted from <strong>the</strong><br />
bed, or because of insufficient care during packing <strong>and</strong> transportation to <strong>the</strong><br />
planting site. Hardening of seedlings can be beneficial be<strong>for</strong>e transplanting<br />
(Bhatia et al., 2001).<br />
From a review by Pareek (2001), it appears that treatment of roots with 250<br />
ppm IBA improves transplanting success. Shifting <strong>the</strong> seedlings within <strong>the</strong><br />
nursery one month after sowing <strong>and</strong> <strong>the</strong>n transplanting <strong>the</strong>m in <strong>the</strong> field after 7<br />
months also results in better survival. None<strong>the</strong>less, overall risks of mortality<br />
remain quite high when transplanting bed raised seedlings. Thus, <strong>the</strong> method of<br />
raising seedlings in nursery beds is not very popular. Seedlings raised that way<br />
are not considered suitable <strong>for</strong> planting under rainfed conditions.<br />
An<strong>o<strong>the</strong>r</strong> way of raising seedlings is through <strong>the</strong> use of containers. Types of<br />
45
containers commonly used are pots, poly<strong>the</strong>ne tubes or bags. In Burkina Faso,<br />
baskets woven with leaves of <strong>the</strong> palm tree Borassus aethiopum are used in<br />
addition to poly<strong>the</strong>ne containers <strong>for</strong> nursery production of fruit tree seedlings.<br />
Containers most commonly used in India are 28 x 23 cm pots, 23 x 10 cm<br />
poly<strong>the</strong>ne bags <strong>and</strong> poly<strong>the</strong>ne tubes of 25 x 10 cm size in 300 gauge (Pareek,<br />
2001). Poly<strong>the</strong>ne containers must be protected from direct sun heat to avoid<br />
rapid disintegration. Protection is done through proper shading in <strong>the</strong> nursery or<br />
by keeping <strong>the</strong> containers buried in sunken beds.<br />
Several seeds are normally sown per container <strong>and</strong> <strong>the</strong>n <strong>the</strong> young seedlings (at<br />
<strong>the</strong> four leaf stage) are pricked out into separate pots be<strong>for</strong>e finally planting in<br />
<strong>the</strong> field. Pareek (2001) reports 8-10 stones sown in a 30 cm pot. In Burkina<br />
Faso, two dehulled seeds are sown per poly<strong>the</strong>ne bag (Bill<strong>and</strong> <strong>and</strong> Diallo,<br />
1991). At <strong>the</strong> time of pricking out, only one seedling is left per container. In<br />
Burkina Faso seedlings two months old were 12 to 21 cm high, with a collar<br />
diameter of 2 to 3 mm (Dao, 1993). Seedlings ready <strong>for</strong> transplanting in <strong>the</strong><br />
field are five-six months old with a height of 36 to 47 cm <strong>and</strong> a collar diameter<br />
of 4 to 5 mm (Bill<strong>and</strong> <strong>and</strong> Diallo, 1991).<br />
Weeds can cause problems, <strong>and</strong> have to be removed from <strong>the</strong> nursery. Weeding<br />
is usually done manually. Pareek (2001) reports that Cyperus rotundus can also<br />
be controlled by application of oxyfluorfan at 0.6 kg.ha -1 or oxadiazon at 1.5<br />
kg.ha -1 without damaging <strong>the</strong> seedlings.<br />
A frequent constraint is de<strong>for</strong>mity of roots which can be severe due to <strong>the</strong> deep<br />
taproot. Root de<strong>for</strong>mities occur in both seed beds <strong>and</strong> containers (Jaenicke <strong>and</strong><br />
Wightman, 1999). Root de<strong>for</strong>mities can be caused by poor pricking out.<br />
Seedlings squeezed into holes that are too short <strong>for</strong> <strong>the</strong> root system will<br />
develop root de<strong>for</strong>mities <strong>and</strong> any roots which are curled upwards will bend<br />
back <strong>and</strong> grow into a ‘knee’ or even a complete loop. In container raised<br />
seedlings, <strong>the</strong> smooth plastic bags cause <strong>the</strong> main root to coil or spiral along <strong>the</strong><br />
walls or at <strong>the</strong> bottom of <strong>the</strong> container. This invariably happens when plants are<br />
left in <strong>the</strong> nursery too long. However, it can happen even to small Ziziphus<br />
seedlings because of <strong>the</strong> deep taproot. Two months old seedlings only 12 – 21<br />
cm high were found to have taproots that were longer than <strong>the</strong> plant height,<br />
reaching 21.5 cm (Dao, 1993).<br />
As with any <strong>o<strong>the</strong>r</strong> tree seedling, root de<strong>for</strong>mities of Ziziphus seedlings should<br />
be cut off be<strong>for</strong>e planting, as <strong>the</strong>y retard plant growth <strong>and</strong> can even result in <strong>the</strong><br />
plant’s death. Root de<strong>for</strong>mities do not correct <strong>the</strong>mselves over time <strong>and</strong> may<br />
even become more acute as <strong>the</strong> tree grows.<br />
An<strong>o<strong>the</strong>r</strong> constraint would relate to seed sowing at depths more than 3 cm. This<br />
causes poor germination.<br />
In addition to proper weeding <strong>and</strong> <strong>the</strong> application of good nursery practice to<br />
46
minimise root de<strong>for</strong>mities, good seedling management to produce balanced<br />
quality plants in <strong>the</strong> nursery means that regular watering is essential.<br />
Fertilisation <strong>and</strong> inoculation with mycorrhizal fungi also have proved<br />
beneficial.<br />
Although Ziziphus species are drought resistant, adequate water supply in <strong>the</strong><br />
nursery is essential. Pareek (2001) reported that maintenance of pre-irrigation<br />
moisture of 80 % in <strong>the</strong> nursery soil has been helpful in <strong>the</strong> development of<br />
over 98 % Chinese jujube seedlings (to be used <strong>for</strong> budding). In India, a major<br />
breakthrough was achieved in <strong>the</strong> early 1990s with <strong>the</strong> development of a device<br />
known as ‘jaltripti’. The device, as described by Pareek (2001), comprises two<br />
ear<strong>the</strong>nware pots of <strong>the</strong> same height but of different diameters joined at <strong>the</strong><br />
base, keeping <strong>the</strong> base of <strong>the</strong> inner pot open <strong>and</strong> that of <strong>the</strong> outer pot closed.<br />
The outer pot can regularly be filled with water. The ber plant is grown in <strong>the</strong><br />
inner pot in a manure/soil mixture. The device results in very good growth of<br />
<strong>the</strong> plants <strong>and</strong> saves 75 % irrigation water.<br />
Under water stress, inoculation of arbuscular mycorrhizae improves ber<br />
seedling growth, nutrient uptake <strong>and</strong> water stress tolerance. Mathur <strong>and</strong> Vyas<br />
(2000) used six arbuscular mycorrhizal species to inoculate 15 day old Z.<br />
mauritiana seedlings subjected to increasing water stress from field capacity to<br />
near wilting point over a period of 16 weeks. The six mycorrhizal species used<br />
<strong>for</strong> inoculation were: Gigaspora margarita, Glomus constrictum, Glomus<br />
fasciculatum, G. mosseae, Sclerocystis rubi<strong>for</strong>mis <strong>and</strong> Scutellospora calospora<br />
maintained on Cenchrus ciliaris. Seedling mycorrhizal dependency was high<br />
<strong>for</strong> all six fungi, ranging from 111 % to 208 %. Compared to non treated<br />
seedlings, nutrient uptake in mycorrhizal plants increased significantly, ranging<br />
115-223 % <strong>for</strong> nitrogen <strong>and</strong> 154-400 % <strong>for</strong> phosphorus, depending on <strong>the</strong><br />
mycorrhizal species. Mycorrhizal plants also showed increased uptake of<br />
potassium <strong>and</strong> accumulation of proline, both of which are known to play<br />
important roles in plant water stress management through stomatal movement<br />
<strong>and</strong> osmotic adjustment respectively. Although <strong>the</strong> magnitude of seedling<br />
incremental growth varied with VAM species, overall growth of inoculated<br />
seedlings was significantly better than <strong>the</strong> non inoculated ones. G.<br />
fasciculatum, <strong>the</strong> most efficient species in <strong>the</strong> experiment, resulted in almost a<br />
doubling of plant dry weight compared with <strong>the</strong> non inoculated plants. It also<br />
enhanced proline content of seedlings by 37 %. Thus, by whatever mechanism<br />
(increasing N <strong>and</strong> P uptake, increasing potassium uptake or by higher proline<br />
accumulation), inoculation of arbuscular mycorrhizal fungi resulted in efficient<br />
water stress tolerance in Z. mauritiana seedlings. Thus, G. fasciculatum could<br />
be of great importance in cultivation of Z. mauritiana in drought prone areas.<br />
Mycorrhizal inoculation combined with <strong>the</strong> application of rock phosphate has<br />
been tested in a series of studies conducted in Burkina Faso to improve Z.<br />
mauritiana seedling growth <strong>and</strong> vigour in <strong>the</strong> nursery (Ba et al., 1998; Guissou,<br />
1996, 2001; Guissou et al., 1998, 2000). Five mycorrhizal species were tested:<br />
47
Glomus aggregatum, G. intraradices, G. manihotis, G. mosseae <strong>and</strong><br />
Acaulospora spinosa in various experiments. All five mycorrhizae increased<br />
seedling height, collar diameter, stem <strong>and</strong> root dry weight. Acaulospora<br />
spinosa, <strong>the</strong> most efficient fungus, increased seedling height by 171 %, stem<br />
dry weight by 309 % <strong>and</strong> total biomass by 374 %. Z. mauritiana seedlings<br />
showed a higher mycorrhizal dependency (78 %) than Tamarindus indica (34<br />
%) or Parkia biglobosa (24 %).<br />
Application of rock phosphate to four month old Z. mauritiana seedlings<br />
significantly increased seedling height <strong>and</strong> biomass, indicating that non<br />
inoculated Ziziphus seedlings were able to utilise phosphate from rock<br />
phosphate. This is important because soils in <strong>the</strong> region are inherently poor <strong>and</strong><br />
particularly deficient in phosphate, whereas rock phosphate is readily available<br />
from large deposits in <strong>the</strong> region.<br />
Raising Z. rotundifolia seedlings <strong>for</strong> rootstocks <strong>and</strong> treatment <strong>and</strong> h<strong>and</strong>ling of<br />
<strong>the</strong> seeds is summarised by (Singh et al., 2001). There are similarities in <strong>the</strong><br />
methodology <strong>for</strong> all Ziziphus species.<br />
5.3 Vegetative propagation<br />
Methods of vegetative propagation differ between Z. mauritiana <strong>and</strong> Z. jujuba.<br />
Traditional methods such as use of cuttings are not successful with <strong>the</strong> <strong>for</strong>mer<br />
whereas in Chinese jujube use of cuttings is, <strong>and</strong> fur<strong>the</strong>rmore Chinese jujube<br />
cuttings can be taken from root suckers be<strong>for</strong>e emergence. Some success has<br />
been observed in ber by stooling. Z. spina-christi is propagated by cuttings.<br />
Budding is <strong>the</strong> major method <strong>for</strong> propagating ber <strong>and</strong> can be successfully<br />
carried out using several methods. Of <strong>the</strong> different methods <strong>the</strong> degree of<br />
success varies according to climatic conditions, time <strong>and</strong> method of budding<br />
<strong>and</strong> <strong>the</strong> skills of <strong>the</strong> operators.<br />
Both ber <strong>and</strong> Chinese jujube can be propagated by grafting, using <strong>the</strong> wedge<br />
method <strong>for</strong> ber <strong>and</strong> <strong>the</strong> whip or tongue method <strong>for</strong> Chinese jujube.<br />
5.3.1 Rootstocks<br />
For ber, rootstocks are ei<strong>the</strong>r <strong>the</strong> same species (wild) or commonly Z.<br />
nummularia (often referred to by its synonym Z. rotundifolia). No<br />
incompatibility is seen between scions of <strong>the</strong> cultivars <strong>and</strong> rootstock seedlings<br />
of Z. nummularia, wild Z. mauritiana, Z. oenoplia, Z. rugosa, Z. xylocarpa, Z.<br />
jujuba or Z. spina-christi (Pareek, 1983). None<strong>the</strong>less vigour <strong>and</strong> growth differ<br />
greatly. Use of Z. nummularia tends to be less favourable <strong>for</strong> fruit production<br />
than <strong>the</strong> use of Z. mauritiana (Pareek <strong>and</strong> Nath, 1996).<br />
48
Z. abyssinica rootstocks can also be used <strong>for</strong> ber <strong>and</strong> are more successful than<br />
Z. spina-christi as <strong>the</strong> latter often produces a bottleneck <strong>for</strong>m (Nerd <strong>and</strong><br />
Mizrahi, 1998). In Africa wild Z. mucronata does not appear useful due to<br />
delayed incompatibility (Kadzere et al., 1997).<br />
Rootstock seedling plants of different species, although from variable<br />
progenies, influence <strong>the</strong> vigour, growth <strong>for</strong>m <strong>and</strong> productivity of <strong>the</strong> scion <strong>and</strong><br />
presumably also its adaptation to adverse climatic <strong>and</strong> soil conditions (Verma<br />
et al. 2001).<br />
The best choice, at present, seems to be to raise rootstocks from seeds collected<br />
from vigorous trees of cultivated ber (Z. mauritiana) <strong>and</strong> boradi (Z. mauritiana<br />
var. rotundifolia) or <strong>o<strong>the</strong>r</strong> suitable wild species such as Z. abyssinica. Use of<br />
vegetatively propagated or seedling plants from identified genotypes of <strong>the</strong><br />
selected species should in due course lead to <strong>the</strong> development of st<strong>and</strong>ard<br />
rootstocks. This will ensure <strong>the</strong> desired effects of adaptability, productivity,<br />
vigour <strong>and</strong> <strong>for</strong>m of <strong>the</strong> scion, <strong>and</strong> longevity of <strong>the</strong> scion/rootstock combination<br />
under different ecological habitats.<br />
In Chinese jujube, seedlings of Z. jujuba var. spinosa <strong>and</strong> <strong>o<strong>the</strong>r</strong> wild species are<br />
used as rootstocks (Ming <strong>and</strong> Sun, 1986). Grafting over 2 cm thick roots of<br />
Paliurus spinosa has also given success (Zaktreger <strong>and</strong> Solov’ev, 1962).<br />
5.3.2 Budding<br />
5.3.2.1 The budwood<br />
Budwood becomes available during <strong>the</strong> active growth period in <strong>the</strong> summer.<br />
The bud sticks, with well swollen <strong>and</strong> recently matured buds (but still not open)<br />
are collected (Fig. 5.1). Immature <strong>and</strong> undeveloped buds from <strong>the</strong> upper part of<br />
<strong>the</strong> new shoots <strong>and</strong> over mature <strong>and</strong> inactive buds should not be used. Buds<br />
collected from flowering shoots give poor success. Buds should be collected<br />
from juvenile shoots. Such shoots can be induced to grow by severe pruning of<br />
<strong>the</strong> m<strong>o<strong>the</strong>r</strong> trees.<br />
49
Figure 5.1 The budwood<br />
After collection, <strong>the</strong> budwood is often stored <strong>for</strong> a time or has to be transported,<br />
<strong>and</strong> considerable loss of viability may take place. Budwood retains good<br />
viability when kept under ventilated conditions <strong>and</strong> wrapped in moist jute<br />
cloth. Kanwar <strong>and</strong> Singh (1981) found that buds stored in poly<strong>the</strong>ne sheeting,<br />
even <strong>for</strong> one day at 31-38° C <strong>and</strong> 67-68% relative humidity, failed in bud-take.<br />
However, buds kept in moist jute cloth <strong>for</strong> one day gave bud-take of 68.8% <strong>and</strong><br />
36.2% when kept <strong>for</strong> five days. Singh (1988) found that budwood wrapped in<br />
poly<strong>the</strong>ne sheeting <strong>and</strong> moist sphagnum moss gave better results than those<br />
stored in moist jute cloth.<br />
5.3.2.2 Time of budding<br />
The best time <strong>for</strong> successful budding is during <strong>the</strong> active growth period. The<br />
active growth period is indicated by easy <strong>and</strong> clear separation of <strong>the</strong> bark from<br />
<strong>the</strong> wood in both scion <strong>and</strong> <strong>the</strong> rootstock. Kaundal et al. (1984) observed<br />
maximum bud-take (80-87 %) at ambient temperature between 30 <strong>and</strong> 34° C,<br />
irrespective of variations in atmospheric relative humidity (RH) from 45 to<br />
73.5 %. Bud-take declines below 36 % RH <strong>and</strong> when temperatures drop to<br />
18.5-20° C. Such conditions occur during <strong>the</strong> summer <strong>and</strong> monsoon period<br />
(June to September) in <strong>the</strong> arid <strong>and</strong> semi-arid subtropics of northwest India<br />
(Joshi, 1960; Singh et al., 1972 b; Pareek. 1978 a; Singhrot et al., 1980; Anon.,<br />
1981; Kaundal et al., 1984; Mawani <strong>and</strong> Singh, 1992 a, b). Maximum<br />
sprouting of 93.2 % has been recorded by budding when <strong>the</strong> maximum<br />
temperature was between 33 <strong>and</strong> 36.5° C <strong>and</strong> minimum temperature was<br />
around 26° C (Kaundal et al., 1984). Some success can be obtained even during<br />
<strong>the</strong> mild winter months of <strong>the</strong> tropics (Jyotishi et al., 1967).<br />
50
5.3.2.3 Transplanting of budded plants<br />
Budded seedlings prepared in nursery beds are lifted with large earth balls at<br />
about 9 to 12 months after budding <strong>for</strong> transplanting to <strong>the</strong> field. A number of<br />
<strong>the</strong>se plants may be lost due to damage while lifting, packaging, during<br />
transport <strong>and</strong> transplanting (see <strong>for</strong> instance, Singh et al., 2001). The operations<br />
are cumbersome <strong>and</strong> incur high costs due to <strong>the</strong> large earth balls. Attempts<br />
have been made to reduce mortality by:<br />
i) shifting <strong>the</strong> plants within <strong>the</strong> nursery 25 days after sprouting (6 leaf stage) to<br />
harden <strong>the</strong>m be<strong>for</strong>e final transplanting at about 8 months after budding<br />
(Singhrot <strong>and</strong> Makhija, 1979 a; Bhatia et al., 2001),<br />
ii) shifting <strong>the</strong> buddings into polybags of 30 x 20 cm size along with treatment<br />
of 12 % Waxol (Kundi <strong>and</strong> Singhrot, 1990),<br />
iii) transplanting <strong>the</strong> defoliated buddings without earth ball during <strong>the</strong> winter in<br />
<strong>the</strong> subtropics (S<strong>and</strong>hu <strong>and</strong> Dhillon, 1983; S<strong>and</strong>hu et al., 1983; Beniwal et al.,<br />
1992),<br />
iv) cutting <strong>the</strong> tap roots along with treatment with 200 ppm IBA (Singh, 1988)<br />
<strong>and</strong> wrapping <strong>the</strong> roots with moist sphagnum moss or jute cloth during<br />
transport to <strong>the</strong> field.<br />
All <strong>the</strong>se methods increase establishment success, but only after irrigation as<br />
transplanting tends to reduce <strong>the</strong> drought-hardy character of ber trees owing to<br />
loss of tap roots.<br />
Buddings prepared in polytubes become ready <strong>for</strong> transplanting at about 30<br />
days after budding. The polytubes with <strong>the</strong> buddings are removed from <strong>the</strong><br />
nursery <strong>and</strong> kept in shade <strong>for</strong> a week. These can <strong>the</strong>n easily be transported <strong>and</strong><br />
transplanted to <strong>the</strong> field with over 90 % survival (Pareek, 1978 b) since <strong>the</strong>re is<br />
little stress or root damage during lifting, transport <strong>and</strong> planting. The roots of<br />
<strong>the</strong> plants do not coil <strong>and</strong>, <strong>the</strong>re<strong>for</strong>e, retain <strong>the</strong> drought-hardy character <strong>and</strong><br />
vigour almost similar to plants raised in situ. For long distance transport soil is<br />
washed from <strong>the</strong> roots of polytube raised buddings <strong>and</strong> covered with sphagnum<br />
moistened with 0.2 g potassium nitrate, 0.8 g calcium nitrate, 0.2 g magnesium<br />
sulphate, 0.2 g hypophosphate <strong>and</strong> 1 ml of 0.5 % ferric tartrate with 0.2 %<br />
Dithane Z-78 (Pareek <strong>and</strong> Vashishtha, 1980).<br />
5.3.2.4 Budding method<br />
Budding can be carried out by different methods such as I or T (shield), or ring<br />
<strong>and</strong> patch (Husain, 1973; Moti <strong>and</strong> Chaturvedi, 1976; Anon., 1981; Mawari<br />
<strong>and</strong> Singh, 1992 a, b), chip (Anon., 1953), flute (Mawari <strong>and</strong> Singh, 1992 a, b)<br />
<strong>and</strong> <strong>for</strong>ked (Jyotishi et al., 1967). However, shield (Singh, 1952; Anon., 1953;<br />
Singh, 1957; Joshi, 1960; Singh, 1964; Jyotishi et al., 1967) <strong>and</strong> patch budding<br />
are <strong>the</strong> most commonly used methods. The ring method needs <strong>the</strong> scion stick to<br />
be of equal diameter to <strong>the</strong> rootstock <strong>and</strong> this limits its use on a large scale.<br />
Using patch budding, 75-85 % success has been obtained (Anon, 1981) (see<br />
Plates 3-6).<br />
51
St<strong>and</strong>ardisation of <strong>the</strong> budding methods has been summarised by Nayak <strong>and</strong><br />
Sen (2000).<br />
Budding should be per<strong>for</strong>med as close to <strong>the</strong> ground level as practicable to<br />
minimise <strong>the</strong> area <strong>for</strong> emergence of sprouts from <strong>the</strong> rootstock portion. Over<br />
93% success has been obtained by budding at <strong>the</strong> height of 10 cm onto<br />
seedlings with a stem diameter of 0.53-0.55 cm (Singh et al., 1981 b;<br />
Chattopadhyay <strong>and</strong> Dey, 1992). Lopping <strong>and</strong> topping of <strong>the</strong> rootstock from 8<br />
(Kundu 1983; Singhrot <strong>and</strong> Kajal, 1986) to 15 days (Singh et al., 1984 c) after<br />
budding in <strong>the</strong> nursery beds has been found to ensure 90 to 100 % success.<br />
Topping has also been found to increase growth of buddings (Anon., 1981).<br />
Pareek et al. (1999) recommend that just be<strong>for</strong>e in situ budding in <strong>the</strong> field,<br />
rootstock seedlings should be lopped at 30-45 cm height.<br />
When budding onto seedlings raised in poly<strong>the</strong>ne tubes, <strong>the</strong> rootstocks should<br />
be prepared by removing all side shoots <strong>and</strong> leaves from <strong>the</strong> stem up to a height<br />
of 15 cm above ground level. The seedlings are <strong>the</strong>n topped just be<strong>for</strong>e budding<br />
using ei<strong>the</strong>r <strong>the</strong> shield or patch method (Fig. 5.2).<br />
2.5 cm patch<br />
Separation of bud from budwood<br />
Patch removed on rootstock<br />
Bud fixed on patch<br />
Patch budding<br />
I-cut on rootstock<br />
Bud inserted into I-cut<br />
Budling ready <strong>for</strong> planting<br />
Shield budding<br />
Tying inserted bud on roostock<br />
Figure 5.2. Methods of budding<br />
52
5.3.3 Micropropagation<br />
Tissue culture techniques offer possibilities of rapid cloning of desired<br />
genotypes. Pareek (2001) provided <strong>the</strong> following summary:<br />
5.3.3.1 <strong>Ber</strong><br />
Goyal <strong>and</strong> Arya (1985) induced adventitious root <strong>for</strong>mation within 20 days in<br />
shoot segments of Gola <strong>and</strong> Seb cultivars, in half strength MS medium<br />
supplemented with 0.5 mg per litre of IBA <strong>and</strong> kinetin. Nearly 60 % of <strong>the</strong><br />
rooted shoots could be successfully transplanted into pots <strong>and</strong> <strong>the</strong> total time<br />
taken from initial culturing to transplantation was 150 days. The protocol<br />
developed by Rathore et al. (1992) involves culturing nodal explants on MS<br />
medium containing 7.5 mg benzyladenine plus 0.1 mg IAA/l <strong>for</strong> shoot<br />
proliferation, <strong>the</strong>n in White’s liquid medium containing 25 mg IBA/litre to<br />
induce rooting <strong>and</strong> <strong>the</strong>n in White’s solid medium without growth regulators<br />
followed by hardening off be<strong>for</strong>e transplanting into pots.<br />
Kabir et al. (1994) multiplied shoots through axillary bud elongation on MS<br />
medium containing 0.1 mg/litre NAA or IAA <strong>and</strong> 2 mg/litre bezyladenine,<br />
which were rooted by transferring <strong>the</strong> shoots to MS medium containing 0.5-2<br />
mg/litre IBA. Large-scale multiplication of shoots can be carried out by<br />
repeated subculturing of <strong>the</strong> nodal segments of in vitro grown shoots after<br />
every 6-8 weeks.<br />
Mathur et al. (1995) grew stem explants from mature trees on MS medium<br />
containing 3800 mg/litre potassium nitrate, 2475 mg/litre ammonium nitrate,<br />
11 mμ-M benzyladenine <strong>and</strong> 0.5 mμ-M IAA, which produced 15-20 shoots per<br />
inoculum on successive subculturing. Rooting in <strong>the</strong> shoots could be induced<br />
by pre-treatment with 50 mμ-M IAA or NAA <strong>for</strong> 24 hours followed by <strong>the</strong>ir<br />
transfer to auxin-free White’s medium <strong>and</strong> <strong>the</strong>n into soil <strong>and</strong> vermiculite<br />
mixture.<br />
Work is proceeding on tissue culture of ber <strong>and</strong> a recent summary was<br />
provided by HU et al. (2001).<br />
5.3.3.2 Chinese jujube<br />
By culturing stem segments of jujube lines A 17, A 27 <strong>and</strong> A 80 in MS<br />
medium containing 1 mg BA per litre, <strong>the</strong> highest percentage of clustered buds<br />
(66.7) was differentiated. Maximum root growth (95.9 %) was induced in <strong>the</strong><br />
medium containing 0.4 mg/litre IBA (Yan et al., 1990). Culture medium<br />
containing 2 mg BA + 0.4 mg BA per litre gave 81.8 % differentiated buds<br />
which could be excised continuously <strong>for</strong> multiplication. Kim <strong>and</strong> Lee (1988)<br />
obtained <strong>the</strong> best shoot <strong>and</strong> root growth from axillary buds of cultivar<br />
Geumsung after eight weeks when 500 mg/litre activated charcoal was added<br />
to half strength MS medium with 0.5 mg/litre benzylaminopurine. 1000<br />
mg/litre activated charcoal was required <strong>for</strong> cultivar Bokjo. Rooting <strong>and</strong> callus<br />
53
growth of Geumsung microshoots increased as IBA concentration was<br />
increased to 3 mg/litre. Rooting was better when treated with paclobutrazol<br />
ra<strong>the</strong>r than with IBA, NAA or Rooton.<br />
For producing rooted plants from shoot tips <strong>and</strong> single bud segments, MS<br />
medium supplemented with IBA was more effective than with IAA or NAA<br />
(Cheong et al., 1987). Kinetin <strong>and</strong> 2iP (0.5 mg/litre) <strong>and</strong> BA (1mg/litre)<br />
increased plant height, number of nodes <strong>and</strong> plant weight. A combination of 1<br />
mg/litre IBA <strong>and</strong> 1 mg/litre BA or 0.5-1.0 mg/litre kinetin also increased plant<br />
height <strong>and</strong> weight. Addition of adenosine sulphate at 40 mg/litre to <strong>the</strong> shoot<br />
tip culture <strong>and</strong> at 80 mg/litre to bud segment culture in MS medium + 1<br />
mg/litre IBA + 1mg/litre BA fur<strong>the</strong>r increased plant height <strong>and</strong> number of<br />
nodes. Charcoal, when added to <strong>the</strong> culture medium decreased root number <strong>and</strong><br />
length.<br />
5.3.3.3 Callus culture<br />
Attempts have been made to regenerate plantlets of Ziziphus cultivars via callus<br />
<strong>for</strong>mation from a range of explants followed by organogenesis <strong>and</strong> somatic<br />
embryogenesis (Cheong <strong>and</strong> Kim, 1984; Kim et al., 1987; Mathur et al., 1993;<br />
Mitrofanova <strong>and</strong> Shevelukka, 1995; Mitrofanova et al., 1994. 1997). This may<br />
not, however, provide a practical technique <strong>for</strong> multiplication of true-to-type<br />
plants, <strong>and</strong> <strong>the</strong>re is a risk of somaclonal variation occurring. More work needs<br />
to be done.<br />
5.3.3.4 O<strong>the</strong>r research<br />
Micrografting has received attention in order to multiply a superior cultivar<br />
through an in vitro micrografting technique which is a miniaturisation of <strong>the</strong><br />
apex slice involving grafting of scions
et al., 1996) have also been observed to induce early rooting <strong>and</strong> to increase<br />
rooting percentage.<br />
In Chinese jujube, cuttings taken from root suckers be<strong>for</strong>e emergence give<br />
76.8% survival (Dong <strong>and</strong> Song, 1988). Root sucker differentiation from<br />
mature trees is 1000 to 15000 per hectare if 15 cm of <strong>the</strong> soil surface layer is<br />
removed in <strong>the</strong> orchard during March-April or September-October. Chinese<br />
jujube suckers when treated be<strong>for</strong>e stooling with 2500 ppm IBA gave 100 %<br />
rooting in s<strong>and</strong>, 66.7 % in vermiculture + perlite <strong>and</strong> 55.6 % in soil medium but<br />
did not root when stooled without IBA treatment (Kim <strong>and</strong> Suh, 1989).<br />
5.3.5 Grafting<br />
5.3.5.1 <strong>Ber</strong><br />
Wedge grafting has been successful <strong>for</strong> propagating ber in Israel (Nerd <strong>and</strong><br />
Mizrahi, 1998); budding is on <strong>the</strong> whole easier to use <strong>and</strong> more economical.<br />
5.3.5.2 Chinese jujube<br />
Chinese jujube is propagated by whip <strong>and</strong> tongue grafting, <strong>and</strong> carried out<br />
during <strong>the</strong> winter when <strong>the</strong> plants are dormant. Slanting 3-5 cm long cuts are<br />
made on both stock <strong>and</strong> scion shoots of equal diameter. The cut ends of <strong>the</strong><br />
stock <strong>and</strong> scion are joined <strong>and</strong> tied. The grafts become ready <strong>for</strong> transplanting<br />
after one year. One year old, primary shoots of Chinese jujube gave <strong>the</strong> best<br />
results <strong>for</strong> in situ grafting during spring on seedling rootstocks planted in <strong>the</strong><br />
field (Kim et al., 1982 b). Cutting back <strong>the</strong> reproductive shoot above <strong>the</strong> third<br />
node in <strong>the</strong> middle of June increased shoot length. Softwood grafting in early<br />
spring also gave success of 90 % (Ivanova, 1976).<br />
55
Chapter 6. Agronomy<br />
(Revised by J.T. Williams)<br />
Propagation to provide planting stocks has been described in Chapter 5. This<br />
chapter covers planting <strong>and</strong> management of orchards or using trees as<br />
intercrops, <strong>and</strong> is mostly devoted to ber.<br />
6.1 Planting<br />
Spots are marked at each site. In India pits of 60 cm 3 size are dug in April or<br />
May <strong>for</strong> planting during <strong>the</strong> monsoon, or December to January <strong>for</strong> spring<br />
planting (Bajwa et al., 1972; Singh et al., 1973 a; Bakhshi <strong>and</strong> Singh, 1974). In<br />
arid areas <strong>the</strong> best time <strong>for</strong> planting is at <strong>the</strong> onset of <strong>the</strong> monsoon (Pareek,<br />
1983).<br />
Pits can be treated to control termites <strong>and</strong> are filled one month be<strong>for</strong>e planting<br />
with a mix of topsoil <strong>and</strong> 15-20 kg farmyard manure. Planting <strong>the</strong>n takes place.<br />
In arid areas this is early but in <strong>o<strong>the</strong>r</strong>s it can extend over two months.<br />
Planting distance depends on soil types, cultivar, climatic conditions <strong>and</strong><br />
amount of training to be imposed on <strong>the</strong> plants. Higher density is possible on<br />
poor soils if training is rigorous. Where possible, drip irrigation is provided<br />
after planting (Singh, 1973 a) <strong>for</strong> <strong>the</strong> first two months. Distances are shown in<br />
Table 6.1.<br />
Table 6.1 Planting distance of ber (after Singh, 1992)<br />
Distance in m<br />
6x6<br />
6x5<br />
5x5<br />
6x4<br />
5x4<br />
6x3<br />
4x4<br />
Plants/ha<br />
277<br />
333<br />
400<br />
416<br />
500<br />
555<br />
625<br />
In Vietnam higher densities are grown; <strong>the</strong> mean number/ha is 625, <strong>the</strong><br />
minimum 555 <strong>and</strong> <strong>the</strong> highest 1000 (Le Thi Thu Hong, 1998). Planting layout<br />
is usually a square pattern.<br />
56
6.1.1 Training of plants: ber<br />
<strong>Ber</strong> has a vine-like downwards growth habit <strong>and</strong> to develop a strong tree<br />
training is essential <strong>and</strong> is carried out usually after <strong>the</strong> first year. Initially trees<br />
can be supported by bamboo sticks. Timing of training varies as described<br />
below.<br />
In subtropical regions, with cold winters <strong>and</strong> warm summers, ber trees are<br />
trained during <strong>the</strong> first three years after planting. During <strong>the</strong> first year, after<br />
planting or in situ budding at <strong>the</strong> onset of monsoon (June-July in India), <strong>the</strong><br />
plants are allowed to grow until <strong>the</strong> following spring (March in India). The<br />
bush is headed back keeping 1-2 basal buds on <strong>the</strong> scion portion just above <strong>the</strong><br />
graft union to induce development of vigorous new shoots. Only one upright<br />
vigorous shoot is allowed to grow from <strong>the</strong> scion bud. The emerging shoot<br />
<strong>for</strong>ms <strong>the</strong> tree trunk in due course. The trunk is kept clean up to 30 cm from<br />
ground level by removing all branches (Pareek, 1978 a). Bajwa <strong>and</strong> Sarowa<br />
(1977) <strong>and</strong> Singh et al. (1973 a), however, recommended that <strong>the</strong> tree trunk<br />
should be kept clean up to 75 cm. From <strong>the</strong> trunk, 3 or 4 well spaced <strong>and</strong><br />
favourably placed branches are allowed to grow. The top of <strong>the</strong> trunk is headed<br />
back during summer (May in India) to encourage growth of <strong>the</strong>se branches<br />
(Fig. 6.1).<br />
Subtropics<br />
Year<br />
June-July<br />
1<br />
March<br />
2<br />
March<br />
2<br />
May<br />
2<br />
March<br />
2<br />
Tropics<br />
Year<br />
June<br />
1<br />
December<br />
2<br />
December<br />
2<br />
February<br />
2<br />
Figure 6.1 Training ber - after planting or in situ budding<br />
July<br />
2<br />
<strong>Ber</strong> has a characteristic growth <strong>for</strong>m producing branches usually starting from<br />
<strong>the</strong> sixth or ninth node from <strong>the</strong> base. Secondary branches <strong>for</strong>m at regular<br />
intervals of three internodes (Reddy <strong>and</strong> Chadha, 1993). During spring or<br />
summer of <strong>the</strong> following year, shoots emerge from <strong>the</strong> basal buds of <strong>the</strong><br />
secondaries <strong>and</strong> grow vigorously but <strong>the</strong> secondaries <strong>the</strong>mselves ei<strong>the</strong>r dry out<br />
57
or remain insignificant. There<strong>for</strong>e, during <strong>the</strong> spring of <strong>the</strong> second year, <strong>the</strong><br />
secondaries are pruned to retain <strong>the</strong>ir basal buds from which vigorous shoots<br />
emerge. More than one shoot may emerge from <strong>the</strong> basal bud, but only one of<br />
<strong>the</strong>se is retained <strong>and</strong> <strong>o<strong>the</strong>r</strong>s are removed. These <strong>for</strong>m <strong>the</strong> main branches of <strong>the</strong><br />
tree frame. On <strong>the</strong> main branches, 3-4 or sometimes 4-6 upright growing <strong>and</strong><br />
properly spaced side shoots are retained <strong>and</strong> <strong>the</strong>n <strong>the</strong> top of <strong>the</strong> main branches<br />
are headed back. During <strong>the</strong> spring of <strong>the</strong> third year, <strong>the</strong>se side shoots are<br />
pruned retaining <strong>the</strong>ir basal buds. From <strong>the</strong>se buds, vigorous shoots emerge to<br />
<strong>for</strong>m <strong>the</strong> sub-main branches of <strong>the</strong> tree frame.<br />
Subtropics<br />
Year<br />
March<br />
3<br />
March<br />
4<br />
March<br />
4<br />
July<br />
5<br />
Tropics<br />
Year<br />
July<br />
2<br />
January<br />
3<br />
January<br />
3<br />
July<br />
3<br />
Figure 6.2 Training in ber. A - trunk, B - main branch, C - Secondary (I<br />
Order sylleptic branch), D - Tertiary (II Order sylleptic branch).<br />
In tropical regions, ber plants continue to grow during <strong>the</strong> winter months <strong>and</strong><br />
thus can be trained within <strong>the</strong> first two years. About 5-6 months after planting,<br />
<strong>the</strong> scion portion is cut back retaining only <strong>the</strong> basal 1-2 buds. From <strong>the</strong> new<br />
growth emerging from <strong>the</strong> scion buds, only one upright growing vigorous shoot<br />
is retained <strong>and</strong> <strong>the</strong> <strong>o<strong>the</strong>r</strong>s are removed. This <strong>for</strong>ms <strong>the</strong> tree trunk. The tree<br />
trunk, main branches <strong>and</strong> sub-main branches are similarly developed as in <strong>the</strong><br />
subtropical region except that <strong>the</strong> intervening growth periods between <strong>the</strong><br />
lopping operations are shorter (about 6 months) compared to about one year in<br />
<strong>the</strong> subtropics.<br />
6.1.2 Chinese jujube<br />
Generally Chinese jujubes are planted at 3.5 x 4 m up to 6 x 6 m. In China rows<br />
are often planted in an intercropping pattern. In Azerbaijan <strong>the</strong>y are more often<br />
orchards (Tagiev <strong>and</strong> Gadzhier, 1990).<br />
58
6.2 Water management<br />
Availability of water is <strong>the</strong> major determinant <strong>for</strong> growth <strong>and</strong> productivity of<br />
all cultivated jujubes.<br />
6.2.1 Rainfed areas<br />
6.2.1.1 Water harvesting<br />
Many ber orchards are found in dry areas <strong>and</strong> depend only on annual rainfall<br />
<strong>for</strong> water. Productivity of <strong>the</strong>se orchards depends mainly upon <strong>the</strong> quantity <strong>and</strong><br />
distribution of rainfall <strong>and</strong> <strong>the</strong> extent of its subsequent use by <strong>the</strong> trees. A<br />
considerable quantity of rain water is lost as runoff <strong>and</strong> cannot be used by <strong>the</strong><br />
trees unless water harvesting methods are employed. These may be in situ<br />
where runoff is concentrated into catchments surrounding a tree or group of<br />
trees, or ex situ where runoff from large rocky areas is diverted directly to<br />
nearby orchards or after collection in reservoirs or farm ponds.<br />
For in situ water harvesting l<strong>and</strong> shaping may be used to prepare sloping<br />
catchments on both sides of <strong>the</strong> rows of ber trees. In <strong>the</strong> subtropical s<strong>and</strong>y<br />
planes, which receive 360 mm annual rainfall in northwest India, higher runoff<br />
yield was obtained from catchments having 5 % slope than from <strong>the</strong> usual l<strong>and</strong><br />
slope of 0.5 % (Yadav et al., 1980; Sharma et al., 1982, 1986). In due course,<br />
<strong>the</strong> s<strong>and</strong>y catchments stabilised as a result of compaction <strong>and</strong> levelling, <strong>and</strong><br />
generated runoff even with rainfall of only 25 mm.<br />
On natural undulating wastel<strong>and</strong>s, trees can be planted at <strong>the</strong> lowermost point<br />
of each microcatchment where runoff accumulates. For this, <strong>the</strong> area is divided<br />
into microcatchment plots of 150 to 500 m 2 each. The size of plots depend<br />
upon <strong>the</strong> required quantity of runoff supplement which in turn depends upon<br />
rainfall, catchment slope, antecedent catchment characters (compaction,<br />
smoothness, etc.) <strong>and</strong> <strong>the</strong> runoff coefficient of <strong>the</strong> soil (Evenari et al., 1971).<br />
Bhati et al. (1997) used rainwater collected in small farm ponds to irrigate ber<br />
trees during <strong>the</strong> fruit development period.<br />
6.2.2 Irrigated areas: ber<br />
Irrigation during early growth can be beneficial. Drip irrigation is most<br />
effective <strong>for</strong> this (Yaragattikar <strong>and</strong> Itnal, 2003). Farmers do not generally<br />
irrigate established ber orchards <strong>o<strong>the</strong>r</strong> than <strong>for</strong> intercrops (Verma <strong>and</strong> Gujar,<br />
1994). However, water deficits decrease <strong>the</strong> productivity of trees by reducing<br />
<strong>the</strong> assimilation rate. In <strong>the</strong> subtropical semi-arid region of north India,<br />
irrigation during <strong>the</strong> fruit development period has been observed to increase<br />
productivity by decreasing fruit drop (Bakhshi <strong>and</strong> Singh, 1974). Although<br />
irrigation during <strong>the</strong> flowering period causes flower shedding in ber (Singh et<br />
al., 1973 a), watering may have to be done if <strong>the</strong>re are prolonged breaks in <strong>the</strong><br />
59
monsoon during <strong>the</strong> growth <strong>and</strong> flowering period. Irrigation at <strong>the</strong> time of fruit<br />
maturity delays <strong>and</strong> prolongs <strong>the</strong> maturity period.<br />
6.2.3 Chinese jujube<br />
Chinese jujube productivity also increases with irrigation (fruit yield increasing<br />
by 60 %: Tagier <strong>and</strong> Gadzhier, 1990). Where irrigation is practised <strong>the</strong>re are<br />
normally about six irrigations in a season.<br />
In both major jujubes saline water up to almost 6 dSm -1 can be used; higher<br />
contents result in a decrease in fruit yield (Jin et al., 1988; Jain <strong>and</strong> Dass,<br />
1988).<br />
6.2.4 Conservation of moisture<br />
Mulching conserves moisture in <strong>the</strong> soil <strong>and</strong> suppresses weed growth. A range<br />
of organic wastes can be used. Normally a bed is prepared around <strong>the</strong> trunk<br />
covering three quarters of <strong>the</strong> area of <strong>the</strong> canopy. Black poly<strong>the</strong>ne sheeting is<br />
also useful <strong>and</strong> <strong>the</strong> most effective treatment (see Pareek <strong>and</strong> Nath, 1996 <strong>for</strong> ber;<br />
<strong>and</strong> Byun et al., 1989, 1991 <strong>and</strong> Ming <strong>and</strong> Sun, 1986 <strong>for</strong> Chinese Jujuba).<br />
A number of chemical sprays have been tested to reduce loss of water through<br />
transpiration. O<strong>the</strong>r chemicals can be watered in <strong>the</strong> soil around <strong>the</strong> trees <strong>for</strong><br />
this purpose. However, <strong>the</strong>y are not yet cost-effective.<br />
6.3 Weeding<br />
Weeding is normally carried out through regular hoeings which are shallow<br />
tillings. Particular attention in all jujube species is paid to removal of root<br />
suckers in order to maintain <strong>the</strong> individual tree.<br />
Annual ploughing of inter-row spaces helps weed control when carried out<br />
after weed emergence, followed by harrowing later.<br />
Herbicides can be used e.g. dalapon followed by paraquat, each at <strong>the</strong> rate of 5<br />
kg/ha (Bajwa et al., 1990) <strong>and</strong> glycophosphate at 4 kg/ha (Bajwa et al., 1993).<br />
6.4 Manure <strong>and</strong> fertilisers<br />
Small orchards are seldom manured. In <strong>the</strong> arid region of northwest India,<br />
farmers do not apply any manure or fertiliser in ber orchards <strong>o<strong>the</strong>r</strong> than that<br />
given at planting time (Verma <strong>and</strong> Gujar, 1994). Regular manuring is,<br />
however, essential to replenish <strong>the</strong> nutrient removal by <strong>the</strong> tree through fruit<br />
harvests <strong>and</strong> annual pruning besides losses from <strong>the</strong> soil. According to Ahlawat<br />
et al. (1990), as many as 75 % of <strong>the</strong> orchards in <strong>the</strong> arid subtropics were<br />
deficient in organic N <strong>and</strong> 90 % in P but none in K. Under subtropical <strong>and</strong><br />
60
tropical agroclimates, nitrogen deficiency is widespread <strong>and</strong> thus it plays a<br />
major role in determining fruit yields . Deficiencies of N, P <strong>and</strong> K reduce shoot<br />
length, leaf number <strong>and</strong> size, axillary branch number, flowering <strong>and</strong> fruit set<br />
<strong>and</strong> consequently productivity of <strong>the</strong> tree (Sadhu et al., 1978).<br />
A ber tree removes from <strong>the</strong> soil, 142 to 191 g N, 59 to 87 g P <strong>and</strong> 467 to 684 g<br />
K on average during a single growing season (Mehrotra et al., 1987). Most is<br />
due to fruit harvesting. According to P<strong>and</strong>ey et al., (1990), 43.8 g N, 7.5 g P,<br />
101.2 g K, 4.5 g Ca <strong>and</strong> 22.7 g Mg are removed by 100 kg harvest of fruits.<br />
Judicious manuring <strong>and</strong> fertilisation are necessary to replace nutrient losses <strong>and</strong><br />
to correct deficiencies due to imbalances in <strong>the</strong> soil or plant. Nitrogen <strong>and</strong><br />
phosphorus fertilisation in <strong>the</strong> light soils of <strong>the</strong> arid <strong>and</strong> semi-arid subtropics is<br />
critical <strong>and</strong> potash may be applied to guard against its possible limitation as a<br />
result of annual removal over several years.<br />
6.4.1 Nutrients recommended<br />
In irrigated ber orchards 20-30 kg FYM or 400-500 g N, 200 g K20 <strong>and</strong> 200 g<br />
P205 can be provided annually when planted widely. In rainfed conditions half<br />
<strong>the</strong>se doses are recommended (Singh, 1992). Actual practices are shown in<br />
Table 6.2<br />
Table 6.2 Nutrient practices in ber orchards in India (amounts in kg)<br />
Manurial Practices Punjab Rajasthan Haryana<br />
Farm yard manure<br />
Year 1 10 10 10<br />
Annual increment 10 10 5<br />
Year 5 onwards -- 50 30<br />
Year 10 onwards 100 -- --<br />
Calcium ammonium nitrate<br />
Year 1 0.5 -- 0.5<br />
Annual increment 0.5 -- 0.5<br />
Year 5 onwards -- -- 2.0<br />
Year 10 onwards ca 5 --<br />
Superphosphate<br />
Year 1 -- -- 0.25<br />
Annual increment -- -- 0.25<br />
Year 5 onwards -- -- 1.00<br />
Bone meal<br />
Year 1 -- 0.25 --<br />
Year 2 -- 0.25 --<br />
Year 3 -- 0.50 --<br />
Source: Singh et al., 1973 a (Punjab); Pareek, 1978 a (Rajasthan); Chundawat <strong>and</strong><br />
Srivastava, 1978 (Haryana).<br />
61
In <strong>the</strong> low fertility soils of arid <strong>and</strong> semi-arid regions, application of organic<br />
manures is considered essential <strong>for</strong> sustained nutrient supply. Organic manures<br />
also enable greater moisture retention <strong>for</strong> longer periods in <strong>the</strong>se light soils.<br />
Similarly, fertilisers having lower losses of nutrients, e.g. calcium ammonium<br />
nitrate ra<strong>the</strong>r than urea, are preferred.<br />
The best results have been obtained in young orchards of cv. Umran by<br />
application of 400 g N + 100 g P + 200 g K per tree (Dhatt et al., 1993); in<br />
established orchards of Umran by application of 750 g N per tree (Dahiya et<br />
al., 1985); in 8 year old orchards of Kaithli by application of 500 g N per tree<br />
(Yamdagni et al., 1980); <strong>and</strong> in 6 year old orchards of Gola cultivar by<br />
application of 1000 g N + 1000 g P + 150 g K per tree (Singh et al., 1986). A<br />
multi-location trial indicated good results by application of 750 g N per tree in<br />
deep s<strong>and</strong>y soils of <strong>the</strong> north-western subtropics <strong>and</strong> by 250 g N per tree in <strong>the</strong><br />
shallow s<strong>and</strong>y loam soils in <strong>the</strong> sou<strong>the</strong>rn tropics of India (Pareek <strong>and</strong> Nath,<br />
1996). Thus, it appears that ber trees require 500 to 1000 g N, 400 to 800 g P<br />
<strong>and</strong> 100 to 200 g K per tree depending upon age of <strong>the</strong> tree <strong>and</strong> edaphic <strong>and</strong><br />
climatic conditions of <strong>the</strong> area.<br />
The method of placement of fertilisers depends on <strong>the</strong> root growth pattern. In<br />
an irrigated orchard, most of <strong>the</strong> active roots of 10-year old ber trees are<br />
located 2.35 m from <strong>the</strong> trunk <strong>and</strong> up to 0.5 m deep (Khera et al., 1981). Under<br />
rainfed conditions, however, <strong>the</strong> roots make more vertical growth down to a<br />
depth of 4.5 m (Pareek, 1977).<br />
6.4.2 Foliar feeding<br />
Under rainfed conditions, foliar feeding is often a practical method of<br />
supplementing nutrient requirements, particularly of nitrogen <strong>and</strong><br />
micronutrients. Nitrogen fertilisation of ber trees through foliar sprays of urea<br />
increased fruit set, fruit retention <strong>and</strong> yield, <strong>and</strong> improved fruit quality in<br />
cultivars Banarsi Karaka (Rajput <strong>and</strong> Singh, 1976; 1977), Umran (Chauhan <strong>and</strong><br />
Gupta, 1985; Singh <strong>and</strong> Ahlawat, 1995) <strong>and</strong> Gola (Joon et al., 1984). Dahiya et<br />
al. (1985) found that application of 375 g N through foliar spray <strong>and</strong> 375 g N to<br />
<strong>the</strong> soil gave a fruit yield of 128-130 kg per tree, higher than by applying all <strong>the</strong><br />
nitrogen ei<strong>the</strong>r through soil or foliage. The optimum concentration of urea <strong>for</strong><br />
foliar application seems to be 1 to 2 % (Joon et al., 1984; Chauhan <strong>and</strong> Gupta,<br />
1985; Dahiya et al., 1985; Singh <strong>and</strong> Ahlawat, 1995). Two sprays may be<br />
required at monthly intervals depending upon <strong>the</strong> nitrogen requirement. The<br />
best time <strong>for</strong> spray application seems to be after <strong>the</strong> fruit has set (Joon et al.,<br />
1984; Chauhan <strong>and</strong> Gupta, 1985; Dahiya et al., 1985; Singh <strong>and</strong> Ahlawat,<br />
1995).<br />
62
Supplementing micronutrients through foliar sprays of 0.2 to 0.4 % ZnSO 4 or<br />
FeSO 4 or MnSO 4 <strong>and</strong> 0.2 % boric acid has been observed to increase TSS <strong>and</strong><br />
ascorbic acid contents (Kamble <strong>and</strong> Desai, 1996). This resulted in development<br />
of golden-yellow ra<strong>the</strong>r than green-yellow fruit colour in tropical regions. In<br />
<strong>the</strong> arid subtropics where zinc deficiency is more common <strong>and</strong> widespread,<br />
higher concentrations of ZnSO 4 , i.e. 0.5 % (Singh <strong>and</strong> Ahlawat, 1995) <strong>and</strong> 0.8<br />
% (Joon et al., 1984) have given a better response.<br />
Combined sprays of micronutrients (0.03 % boric acid <strong>and</strong> 0.5 % ZnSO 4 ) <strong>and</strong><br />
growth regulator (50 ppm NAA) have been found to improve fruit quality in<br />
ber by increasing total soluble solids, total sugars <strong>and</strong> ascorbic acid <strong>and</strong><br />
decreasing acidity (Singh et al., 1989 a, b).<br />
In Chinese jujube 200 ppm e<strong>the</strong>phon along with urea sprays accelerated<br />
movement of nitrogen from leaves to <strong>o<strong>the</strong>r</strong> parts of <strong>the</strong> tree <strong>and</strong> increased <strong>the</strong><br />
length of fruit bearing branches, fruit set <strong>and</strong> fruit weight (Hao <strong>and</strong> Zeng,<br />
1991).<br />
6.4.3 Microbial inoculations<br />
Microbial inoculations of soil <strong>and</strong> ber roots with Azospirillum, Azotobacter<br />
(Rao <strong>and</strong> Dass, 1989), vesicular arbuscular mycorrhizal fungi (VAM) (Mathur<br />
<strong>and</strong> Vyas, 1995 a,b,c,d; 1996) <strong>and</strong> <strong>o<strong>the</strong>r</strong> nitrogen fixing actinomycetes (Tuohy<br />
et al., 1991) can help in effective nutrient management. Soil inoculation with<br />
cell suspensions of Azospirillum brasilense strains S 14 , S 51 <strong>and</strong> S 54 or<br />
Azotobacter chroococcum increased height <strong>and</strong> weight of young plants of cv.<br />
Gola (Rao <strong>and</strong> Dass, 1989).<br />
6.5 Pruning<br />
Pruning is essential to maintain vigour in <strong>the</strong> trees <strong>and</strong> to maintain fruit<br />
productivity, quality <strong>and</strong> size.<br />
Fruit bearing in ber is on <strong>the</strong> current season’s shoots (Singh et al., 1970;<br />
Pareek, 1983) <strong>and</strong> remains confined to <strong>the</strong> secondary <strong>and</strong> tertiary branches<br />
(Reddy, 1983). Pruning should <strong>the</strong>re<strong>for</strong>e induce <strong>the</strong> emergence of a maximum<br />
number of secondaries <strong>and</strong> tertiaries on vigorous shoots. This can be done by<br />
pruning at <strong>the</strong> right time <strong>and</strong> with <strong>the</strong> right intensity depending upon location<br />
<strong>and</strong> cultivar.<br />
6.5.1 Pruning intensity<br />
The severity of annual pruning is determined by <strong>the</strong> length of <strong>the</strong> past season’s<br />
shoot retained after <strong>the</strong> pruning operation, e.g. 20 or 25 cm (very severe), 40 or<br />
50 or 60 cm (severe), 70 or 75 or 90 cm (moderate), 100 or 120 or 125 cm<br />
(light), 150 cm (very light) (Singh et al., 1978 b; Gupta <strong>and</strong> Singh, 1979; Lal<br />
63
<strong>and</strong> Prasad, 1979; 1980 a, b, c; 1981; Dhaliwal <strong>and</strong> S<strong>and</strong>hu, 1984; Bajwa et al.,<br />
1986, 1987; Syamal <strong>and</strong> Rajput, 1989; Nanthakumar, 1991). However, <strong>the</strong><br />
severity of pruning varies depending on <strong>the</strong> vigour of <strong>the</strong> shoot (total length<br />
<strong>and</strong> diameter). An alternative approach has been to base light, moderate <strong>and</strong><br />
severe pruning on removal of one-quarter, half <strong>and</strong> three-quarters of <strong>the</strong> length<br />
of <strong>the</strong> shoot respectively (Sharma, et al., 1980; Singh <strong>and</strong> Godara, 1985; Yadav<br />
<strong>and</strong> Godara, 1987, 1992). The three severity levels have also been based on<br />
pruning <strong>the</strong> shoot at a point where it is 1, 2 or 3 cm in diameter (Bisla et al.,<br />
1988, 1990, 1991).<br />
With increasing pruning severity, <strong>the</strong> shoot (length <strong>and</strong> width) increases (Gupta<br />
<strong>and</strong> Singh, 1979; Singh <strong>and</strong> Godara, 1985; Bisla et al., 1988; Syamal <strong>and</strong><br />
Rajput, 1989) <strong>and</strong> produces a larger number of secondary <strong>and</strong> tertiary branches<br />
(Bisla et al., 1990). Lal <strong>and</strong> Prasad (1979) <strong>and</strong> Dhaliwal <strong>and</strong> S<strong>and</strong>hu (1984)<br />
reported that <strong>the</strong> growth in terms of number of shoots, shoot length <strong>and</strong><br />
diameter was greatest using moderate pruning. Moderate pruning also induces<br />
maximum flowering (Lal <strong>and</strong> Prasad, 1980 a), fruit set <strong>and</strong> fruit retention (Lal<br />
<strong>and</strong> Prasad, 1980 a; Dhaliwal <strong>and</strong> S<strong>and</strong>hu, 1984; Gupta et al., 1990; Yadav <strong>and</strong><br />
Godara, 1992) <strong>and</strong> severe pruning decreases <strong>the</strong> number of flowers per cyme<br />
(Dhaliwal <strong>and</strong> S<strong>and</strong>hu, 1984), fruit set <strong>and</strong> retention (Syamal <strong>and</strong> Rajput, 1989;<br />
Yadav <strong>and</strong> Godara, 1992) <strong>and</strong> delayed fruit maturity (Yadav <strong>and</strong> Godara,<br />
1992). Light pruning reduces fruit drop (Lal <strong>and</strong> Prasad, 1980 c) <strong>and</strong> increases<br />
fruit set <strong>and</strong> retention (Bajwa et al., 1986). Pruning has been observed to<br />
increase leaf area (Singh <strong>and</strong> Godara, 1985; Bisla et al., 1990; Nanthakumar,<br />
1991).<br />
Fruit yield falls as pruning severity increases, <strong>and</strong> is at its lowest in unpruned<br />
trees (Dhaliwal <strong>and</strong> S<strong>and</strong>hu, 1984; Bajwa et al., 1986, 1987; Syamal <strong>and</strong><br />
Rajput, 1989; Kundu et al., 1995). Dinesh (2002) has reported on pruning<br />
intensity especially in semi-arid conditions. The best results have been obtained<br />
by moderate to light pruning in terms of yield <strong>and</strong> quality of fruits (Singh et al.,<br />
1978 b; Lal <strong>and</strong> Prasad, 1979, 1980 b, c, 1981; Sharma et al., 1980; Gupta <strong>and</strong><br />
Godara, 1989; Islam, 1989; Gupta et al., 1990; Bisla et al., 1991).<br />
Reddy (1983) observed that if <strong>the</strong> nodes up to <strong>the</strong> fourth or sixth secondaries<br />
(17-23 nodes) on <strong>the</strong> main axis are induced to sprout by pruning, vigorous<br />
shoots giving maximum fruit yield are produced. Also <strong>the</strong> new growth from <strong>the</strong><br />
nodes on <strong>the</strong> main axis is significantly more productive than that from <strong>the</strong><br />
secondaries. The secondaries should <strong>the</strong>re<strong>for</strong>e be completely removed at <strong>the</strong><br />
time of pruning. Multilocation trials have confirmed <strong>the</strong>se results (Pareek <strong>and</strong><br />
Nath, 1996), <strong>and</strong> it has been recommended that <strong>the</strong> main axis should be pruned<br />
at 15 to 25 nodes depending upon agroclimatic conditions, i.e. at 20-25 nodes<br />
in arid areas <strong>and</strong> at 15 nodes in semi-arid or more moderate regions, along with<br />
complete removal of secondaries.<br />
64
There are some differences according to cultivar. Mukherjee <strong>and</strong> Soni (1993)<br />
obtained best fruit production by pruning to <strong>the</strong> sixth secondaries (25 nodes) in<br />
cv. Seo. Kundu et al. (1995) found that pruning up to 15 nodes was best in cv.<br />
Umran.<br />
Old, unpruned, jujube species can be rehabilitated by reducing overlapping<br />
branches <strong>and</strong> precipitate fruit bearing towards <strong>the</strong> outer part of <strong>the</strong> crown. Half<br />
<strong>the</strong> number of shoots on a tree are pruned at 15 to 25 nodes depending upon<br />
cultivar, <strong>and</strong> <strong>the</strong> remaining half are pruned severely retaining only <strong>the</strong> basal<br />
node (Anon., 1989 b; Kundu et al., 1995). From <strong>the</strong> basal node of <strong>the</strong> severely<br />
pruned shoots, vigorous foundation shoots emerge which during <strong>the</strong> next year<br />
are pruned at 15 or 25 nodes while <strong>the</strong> remaining half are pruned severely. This<br />
pattern of pruning helps to maintain sustainable production as well as tree<br />
<strong>for</strong>m. Even 30 year old trees can be brought back to bearing (Bal et al., 2004)<br />
Kurian (1985) was able to induce early bud break <strong>and</strong> increase <strong>the</strong> number of<br />
vigorous sprouts by a pre-pruning spray of 3% thiourea combined with two<br />
post-pruning sprays of 100 ppm benzyladenine or 50 ppm TIBA at monthly<br />
intervals. A pre-pruning spray (be<strong>for</strong>e 48 h) with 3% thiourea <strong>and</strong> <strong>the</strong>n pruning<br />
half <strong>the</strong> shoots at 25 nodes <strong>and</strong> <strong>the</strong> remaining half to <strong>the</strong> previous season’s<br />
growth gave <strong>the</strong> highest fruit yield of 128 kg/tree.<br />
6.5.2 Pruning in Chinese jujube<br />
Tian et al. (1983) described pruning, one year after training, by cutting back<br />
long branches (over 2 m) <strong>and</strong> by nipping terminal buds. All secondary branches<br />
on <strong>the</strong> main stem are retained to increase <strong>the</strong> number of bearing spurs. During<br />
<strong>the</strong> fourth year, <strong>the</strong> main stems are ringed or notched <strong>and</strong> sprayed with 10 ppm<br />
GA. Plant height is determined by pruning in Chinese jujube. There are<br />
advantages in keeping trees below 3 m height.<br />
6.5.3 Pruning time<br />
Whereas Chinese jujube is pruned in summer <strong>the</strong> time of pruning in Indian<br />
jujube varies in different climates. In subtropical regions, <strong>the</strong> most appropriate<br />
time is during summer (between May <strong>and</strong> June in parts of India) when <strong>the</strong> trees<br />
shed <strong>the</strong>ir leaves <strong>and</strong> enter dormancy (Nijjar, 1972, 1975; Singh <strong>and</strong> S<strong>and</strong>hu,<br />
1984; Gupta <strong>and</strong> Godara, 1989; Gupta et al., 1990; Kundu et al., 1995) <strong>and</strong><br />
be<strong>for</strong>e putting <strong>for</strong>th new growth. Early pruning has been observed to advance<br />
flowering <strong>and</strong> fruit maturity (Singh <strong>and</strong> S<strong>and</strong>hu, 1984; Pareek <strong>and</strong> Nath, 1996).<br />
In tropical regions with a mild winter <strong>and</strong> rainfall during December-January<br />
<strong>and</strong> early onset of summer rainfall (e.g. Tamil Nadu), pruning can be carried<br />
out any time from January to April. It is also possible to regulate fruit maturity<br />
so that bearing occurs at <strong>the</strong> desired time (Pareek <strong>and</strong> Nath, 1996). In tropical<br />
regions without winter rainfall (e.g. Andhra Pradesh), pruning during <strong>the</strong> first<br />
65
two weeks of April results in early flowering <strong>and</strong> <strong>the</strong>re<strong>for</strong>e early harvest;<br />
however, <strong>the</strong> maximum yield of good quality fruits is obtained by pruning in<br />
<strong>the</strong> second two weeks of April (Ramadevi, 1989). In Maharashtra, <strong>the</strong> best time<br />
<strong>for</strong> pruning is be<strong>for</strong>e <strong>the</strong> end of April (Pareek <strong>and</strong> Nath, 1996; Deotate et al.,<br />
1997) as fur<strong>the</strong>r delay causes reduction in fruit yield.<br />
6.6 Pests<br />
There are six major insect pests described below. A few <strong>o<strong>the</strong>r</strong>s are listed <strong>and</strong> a<br />
comprehensive list is provided in Appendix I.<br />
6.6.1 Fruitfly<br />
Carpomyia vesuviana, Dacus correctus <strong>and</strong> D. dorsalis (Diptera: Tephritidae)<br />
infest ber fruits (Basha, 1952; Batra, 1953; Saen, 1986). Carpomyia vesuviana<br />
has been observed to damage as much as 80% of <strong>the</strong> crop under severe<br />
infestations (Cherian <strong>and</strong> Sunderam, 1941). It is <strong>the</strong> most serious pest of ber.<br />
(see Plate 7)<br />
Infestation starts with <strong>the</strong> onset of fruit setting. The adult female lays eggs<br />
singly by inserting its ovipositor in <strong>the</strong> young developing fruit. After 2 to 5<br />
days, <strong>the</strong> larvae hatch, start feeding on <strong>the</strong> pulp <strong>and</strong> make galleries in it.<br />
Generally, only one larva is found in one fruit. The excreta of <strong>the</strong> larva<br />
accumulate in <strong>the</strong> galleries, which may sometimes result in rotting of <strong>the</strong> fruit.<br />
Infested fruits become de<strong>for</strong>med <strong>and</strong> <strong>the</strong>ir growth becomes checked. A large<br />
number of such fruits drop off. The larval stage lasts 9 to 12 days. When full<br />
grown (6 mm length), <strong>the</strong> larva finds its way out by making a hole in <strong>the</strong> fruit<br />
skin <strong>and</strong> drops to <strong>the</strong> ground. The larva bores down into <strong>the</strong> soil up to a depth<br />
of 2 to 12 cm where it pupates. The pupal period lasts about 2 weeks after<br />
which <strong>the</strong> adult fly (5 to 8 mm long, 3 mm broad) emerges. There may be 2 or<br />
3 generations of <strong>the</strong> pest during <strong>the</strong> active period (Batra, 1953), while <strong>the</strong> fruit<br />
matures (from November to April in north India).<br />
6.6.1.1 Prophylaxis<br />
To prevent infestation, prophylactic sprays can be carried out with 0.03 %<br />
oxidematon or dimethoate starting from <strong>the</strong> stage when 70-80 % fruits attain<br />
pea size <strong>and</strong> <strong>the</strong>n repeating <strong>the</strong> spray at one-month intervals (Pareek <strong>and</strong> Nath,<br />
1996). During <strong>the</strong> maturity of fruits, if necessary, spraying should be done with<br />
0.5% Malathion + 0.05% sugar solution at weekly intervals. Malathion has<br />
been observed to dissipate quickly in ber fruits decreasing well below <strong>the</strong><br />
tolerance level of 3 ppm within 2 days after spraying (Popli et al., 1980).<br />
6.6.1.2 Control<br />
Cultivation of <strong>the</strong> orchard soil during spring (Singh et al., 1973 a), summer<br />
(Chundawat <strong>and</strong> Srivastava, 1978) <strong>and</strong> rainy season (Bakhshi <strong>and</strong> Singh, 1974)<br />
destroys <strong>the</strong> hibernating pupae by exposing <strong>the</strong>m to bright sunlight <strong>and</strong> birds<br />
66
<strong>and</strong> thus <strong>the</strong> extent of infestation is considerably reduced. Heating <strong>the</strong> soil by<br />
burning grass <strong>and</strong> irrigation during <strong>the</strong> summer also kills <strong>the</strong> pupae. Infested<br />
fruits having larvae should be collected <strong>and</strong> buried.<br />
Infected fruit have to be collected <strong>and</strong> destroyed. The pest has been effectively<br />
controlled by insecticidal spray schedules such as,<br />
i) three applications of 0.1 % fenthion or two sprays of Endosulfan or<br />
Malathion (Chundawat <strong>and</strong> Srivastava, 1978; Patel et al., 1989),<br />
ii) 0.005 % Fenvalerate or 0.0015 % deltamethrin or 0.05 % monocrotophos or<br />
phosphamidon (Bagle, 1992),<br />
iii) two applications with 0.1 % Dichlorvos, one at pea stage of fruit <strong>and</strong><br />
an<strong>o<strong>the</strong>r</strong> after one month (Raghumoorthi <strong>and</strong> Arumugam, 1992) <strong>and</strong><br />
Monocrotophos or Phosphamidon + carbaryl treatments (Patel <strong>and</strong> Patel,<br />
1979).<br />
Recent data on <strong>the</strong> efficiency of insecticides to control fruit fly have been given<br />
by Gyi et al,.(2003) <strong>and</strong> Gyi et al., (2003a) .<br />
6.6.1.3 Resistant cultivars<br />
Mann <strong>and</strong> Bindra (1976) reported that cultivars Sanaur-1, Safeda Selected,<br />
Illaichi, Mirchia, ZG-3 <strong>and</strong> Umran resisted fruitfly damage. Singh (1984 b)<br />
observed that <strong>the</strong> extent of infestation varied between cultivars from 6.7 % in<br />
Tikadi to 73 % in Gola, Gola Gurgaon-3 <strong>and</strong> Kaithli (Singh <strong>and</strong> Vashishtha,<br />
1984) <strong>and</strong> that <strong>the</strong> percentage of larvae hatched also varied indicating varying<br />
degrees of resistance .<br />
6.6.1.4 Biological control<br />
This has not yet been developed. However, Bracon fletcheri, Opius carpomyiae<br />
<strong>and</strong> Omphalina sp. (Hymenoptera: Braconidae) have been recorded to<br />
parasitise fruitfly but could not provide effective control (Saxena <strong>and</strong> Rawat,<br />
1968). Biosteres carpomyiae <strong>and</strong> Opius fletcheri (Hymenoptera: Braconidae)<br />
are also reported to parasitise fruitfly.<br />
6.6.2 Fruit borer<br />
Damage by larvae of <strong>the</strong> fruit borer moth Meridarchis scyrodes (Lepidoptera:<br />
Carposinidae) has been observed mainly in sou<strong>the</strong>rn <strong>and</strong> western India<br />
(Sonawane <strong>and</strong> Dorge, 1971; Pareek <strong>and</strong> Nath, 1996). The reddish larvae bore<br />
into <strong>the</strong> fruit <strong>and</strong> feed on <strong>the</strong> pulp. The moths are dark brown.<br />
6.6.2.1 Control<br />
Chemical control consists of <strong>the</strong> following: first spray at pea stage with<br />
Monocrotophos (0.03 %), second spray after 15 days with Fenthion (0.05 %)<br />
<strong>and</strong> a third spray 15 days after <strong>the</strong> second spray with 0.01 % Carbaryl has been<br />
recommended (Pareek <strong>and</strong> Nath, 1996).<br />
67
Collection <strong>and</strong> destruction of fallen fruits <strong>and</strong> digging <strong>the</strong> orchard soil under<br />
<strong>the</strong> tree canopy have also given good control. Microbracon sp. (Hymenoptera:<br />
Braconidae), <strong>and</strong> Opius carpomyiae (Hymenoptera: Braconidae) have been<br />
found to parasitise <strong>the</strong> borer. Resistant cultivars Banarsi Pew<strong>and</strong>i, Ajmeri, Gola<br />
Gurgaon <strong>and</strong> Jhajjar Selection have been found to be resistant to <strong>the</strong> pest.<br />
6.6.3 Bark eating caterpillar<br />
The caterpillars of Indarbela quadrinotata, I. watsoni <strong>and</strong> I. tetraonis<br />
(Coleoptera: Cerambycidae) have been reported to make winding galleries of<br />
frassy web on <strong>the</strong> stem near <strong>the</strong> <strong>for</strong>ks <strong>and</strong> angles of branches. The caterpillar is<br />
hidden in <strong>the</strong> stem in <strong>the</strong> day-time <strong>and</strong> becomes active at night, eating <strong>the</strong> bark.<br />
Heavy infestation by this pest stunts <strong>the</strong> trees <strong>and</strong> adversely affects fruit yield.<br />
The moth is pale with grey marks on <strong>the</strong> <strong>for</strong>ewings. It lays eggs with <strong>the</strong> onset<br />
of <strong>the</strong> rainy season in batches of 15 to 25. A single female moth can lay 300 to<br />
400 eggs. Incubation period lasts 8 to 10 days. After emerging, <strong>the</strong> caterpillars<br />
start devouring <strong>the</strong> bark. The dark brown, full-grown caterpillar is 37 to 50 mm<br />
long <strong>and</strong> has a dark head; its body is covered with long, thin hairs. The<br />
caterpillars pupate during <strong>the</strong> summer <strong>for</strong> about four weeks <strong>and</strong> from <strong>the</strong> pupae<br />
adult moths emerge, mate, <strong>and</strong> lay eggs again.<br />
6.6.3.1 Control<br />
Frassy galleries caused by <strong>the</strong> pest need to be removed <strong>and</strong> cleaned. Then<br />
0.05% Monocrotophos is painted on <strong>the</strong> bark, followed by 0.2 % Trichlophos<br />
<strong>and</strong> 0.05 % Chlorofenvinsphos (Verma <strong>and</strong> Singh, 1975). Application of <strong>the</strong><br />
solution, made up by mixing one litre of kerosene <strong>and</strong> 100 g soap in 9 litres of<br />
water, to <strong>the</strong> holes has been found to effectively control <strong>the</strong> bark eating<br />
caterpillar. Alternatively, each hole should be filled with a solution of 2 ml<br />
Monocrotophos or 20 ml Trichlorphon 50 EC or 30 ml Endosulfan 35 EC in 10<br />
litres of water <strong>and</strong> <strong>the</strong>n <strong>the</strong> holes closed with mud. The Dipteran, Zenillia<br />
heterusiae (Diptera: Tachinidae) parasitises I. quadrinotata.<br />
6.6.3.2 Resistant cultivars<br />
Singh (1984 a) found no cultivars that are resistant. However, pest-tolerant<br />
cultivars include, Rohtak Gola, Laddu Glory, Chuhara <strong>and</strong> Desi Alwar. Gola,<br />
Kaithli, Illaichi are susceptible (Verma <strong>and</strong> Singh, 1974; Mann <strong>and</strong> Bindra,<br />
1977).<br />
6.6.4 Hairy caterpillars<br />
Hairy caterpillars (Dasychira mendosa, Euproctis fraterna (Lepidoptera:<br />
Lamantriidae), Thiacidas postica (Lepidoptera: Noctuidae)) feed on <strong>the</strong> young<br />
leaves <strong>and</strong> fruits. The older caterpillars spread in all directions <strong>and</strong> devour<br />
leaves <strong>and</strong> fruits <strong>and</strong> sometimes even tender shoots. They start eating new<br />
foliage as it grows after pruning <strong>and</strong> this is continued by overlapping<br />
68
generations. The full-grown larva is reddish brown with a dark brown head.<br />
The larva pupates on <strong>the</strong> plant in a yellowish, hairy cocoon from which a<br />
yellowish moth with pale transverse lines on <strong>the</strong> <strong>for</strong>ewings emerges. It <strong>the</strong>n<br />
lays flat, circular yellowish eggs in masses on <strong>the</strong> lower surface of <strong>the</strong> leaves.<br />
The females lay 92-241 eggs, which hatch in 9-14 days (Bhatnagar <strong>and</strong> Lakra,<br />
1992). The pre-oviposition, oviposition <strong>and</strong> post-oviposition periods last 2, 1<br />
<strong>and</strong> 4 days respectively, <strong>and</strong> <strong>the</strong> larval, pre-pupal, pupal <strong>and</strong> adult stages last<br />
25-56, 2-3, 7-15 <strong>and</strong> 5-7 days respectively. As many as six generations each of<br />
44-84 days’ duration have been observed in a year.<br />
6.6.4.1 Control<br />
BHC 10 % can be dusted to control caterpillars in <strong>the</strong> young stages. All <strong>the</strong><br />
instars were controlled by treatment with 0.1 % Carbaryl or Endosulfan or<br />
Trichlorphon or 0.05 % Methyl parathion (Verma et al., 1972). Bhatnagar <strong>and</strong><br />
Lakra (1992) obtained <strong>the</strong> most effective control of 3 rd to 6 th instar larvae by<br />
0.005 % Cypermethrin, 0.0014 % Deltamethrin, 0.0075 % Fluvalinate <strong>and</strong><br />
0.0005 % Fenvalerate. A spray of 0.05 % Monocrotophos <strong>and</strong> 0.2 % Carbaryl<br />
(Killex carbaryl 50WP) was found most effective in controlling <strong>the</strong> pest<br />
(Pareek <strong>and</strong> Nath, 1996).<br />
The hairy caterpillar is parasitised by Apanteles taprobanae (Hymenoptera:<br />
Braconidae), Brachymeria sp. (Hymenoptera: Chalcididae), Charops obtusus<br />
<strong>and</strong> Goryphus sp. (Hymenoptera: Ichneumonidae). Exorista species has<br />
recently been found to be a parasitoid of <strong>the</strong> caterpillar in Karnataka (Mani et<br />
al., 2001).<br />
6.6.5 Chafer beetle (ber beetle or leaf chafer)<br />
Chafer beetles (Adoretus decanus, A. kanarensis, A. stoliezkae, A. pallens, A.<br />
versutus) (Coleoptera: Scarabaeidae) devour ber leaves mainly during <strong>the</strong><br />
night. They become active with <strong>the</strong> onset of <strong>the</strong> rainy season when new growth<br />
starts. Leaves become like sieves <strong>and</strong>, in severe cases, <strong>the</strong> whole tree is<br />
rendered leafless. Eggs are laid in <strong>the</strong> soil during <strong>the</strong> early part of <strong>the</strong> rainy<br />
season (May to August in north India). Larvae hatch out in one week <strong>and</strong> feed<br />
on roots <strong>and</strong> vegetation. Adults emerge with <strong>the</strong> onset of rains. There is only<br />
one generation per year.<br />
6.6.5.1 Control<br />
Beetles can be controlled effectively by spraying 0.2 % Carbaryl 50WP <strong>and</strong><br />
0.05 % Monocrotophos (Pareek <strong>and</strong> Nath, 1996). Adoretus pallens can be<br />
controlled by spraying 1 % lead arsenate (Trehan, 1956). The beetles can be<br />
trapped by using any source of light <strong>and</strong> killed by dropping <strong>the</strong>m into water<br />
containing kerosene.<br />
69
6.6.6 Lac insect<br />
<strong>Ber</strong> is a host of <strong>the</strong> lac insects, Kerria lacca <strong>and</strong> K. sindica (Li <strong>and</strong> Hu, 1994).<br />
The small insects become active in summer (April-May). They secrete a thick,<br />
resinous substance which envelopes <strong>the</strong>ir bodies. The secretions <strong>for</strong>m a hard<br />
crust on <strong>the</strong> twigs, which is collected to <strong>for</strong>m a commercial resin, lac. Lac<br />
production is an important business in India. However, <strong>the</strong> insect devitalises<br />
<strong>the</strong> tree <strong>and</strong> causes great loss in fruit production. It sucks <strong>the</strong> sap from <strong>the</strong><br />
branches, <strong>and</strong> ultimately kills <strong>the</strong> tree. An infestation of 5000 nymphs/100 cm<br />
twigs caused a loss of 52.5-58.5 % fruit yield (Lakra <strong>and</strong> Kher, 1990).<br />
Obviously production of lac <strong>and</strong> fruits cannot be done simultaneously (see<br />
Plate 8).<br />
6.6.6.1 Control<br />
Infected twigs should be cut off at <strong>the</strong> time of annual pruning <strong>and</strong> destroyed. If<br />
required, this can be repeated after about 3 months. After pruning, <strong>the</strong> trees<br />
should be sprayed with 0.1 % Dimethoate or 0.03 % phosphamidon. The lac<br />
insect is parasitised by several wasp species, two species of moths <strong>and</strong> 3<br />
species of lacewing flies. Cultivar Gola was found to be <strong>the</strong> most susceptible<br />
cultivar to <strong>the</strong> attack of lac insect followed by Kaithli <strong>and</strong> Umran (Lakra <strong>and</strong><br />
Kher, 1990).<br />
6.6.7 O<strong>the</strong>r insect pests<br />
The following may also cause damage on ber:<br />
Leaf Hopper<br />
Mealy Bug<br />
Weevil<br />
Leaf Gall<br />
Wax Scale<br />
Zyginida pakistanica<br />
Droschiella tamarindus<br />
Xanthochelus supercilosus<br />
Phyllodiplosis jujubae<br />
Drepanococcus chiton<br />
6.6.8 Mites<br />
Mites produce galls in floral buds preventing fruit production (Yamdagni <strong>and</strong><br />
Gill, 1968). The mite, Eriophes cernuus occurs in India throughout <strong>the</strong> year<br />
(Mukherjee et al., 1994). Galled tissues contain higher total carbohydrates <strong>and</strong><br />
reducing sugars <strong>and</strong> more -amylase activity compared to <strong>the</strong> normal tissue<br />
(T<strong>and</strong>on <strong>and</strong> Arya, 1979). Treatment with 0.04 % dicofol gave <strong>the</strong> best control.<br />
The fungus, Fusarium demicellulare is found on <strong>the</strong> galls <strong>and</strong> this seems to<br />
check <strong>the</strong> development <strong>and</strong> spread of galls during <strong>the</strong> initial stages (Singh <strong>and</strong><br />
Singh, 1978).<br />
Incidence of <strong>the</strong> mite Larvacarus transitans can be high during June. Cultivar<br />
Sev was <strong>the</strong> most susceptible (Sharma, 1992). The population of <strong>the</strong> red mite<br />
was least on <strong>the</strong> leaves of cultivar Kaithli (Pareek <strong>and</strong> Nath, 1996).<br />
70
6.7 Diseases<br />
6.7.1 Powdery mildew<br />
Powdery mildew (Oidium erysiphoides f. sp. ziziphi) causes great losses in ber<br />
in India, particularly in humid areas, <strong>and</strong> also in Africa. While most of <strong>the</strong><br />
cultivars were observed to be susceptible at a humid location in sou<strong>the</strong>rn India,<br />
31 out of 66 cultivars observed by Lodha et al., (1984), under <strong>the</strong> arid<br />
conditions of northwest India, did not show any symptoms of <strong>the</strong> disease.<br />
Maximum development of powdery mildew occurs when <strong>the</strong> maximum<br />
temperature is between 24-35 o C, minimum temperature between 4-22 o C,<br />
morning RH 64-91 % <strong>and</strong> evening RH 24-57 % (Pareek <strong>and</strong> Nath, 1996).<br />
Cultivar Umran was studied <strong>and</strong> similar results obtained (Thind et al. 2004).<br />
The disease occurs with increased virulence during high rainfall years (Sharma,<br />
2003), <strong>and</strong> disease incidence can relate to time of pruning as well as to wea<strong>the</strong>r<br />
(Jamadar <strong>and</strong> Venkatesh., 2003).<br />
The symptoms of <strong>the</strong> disease are noticed on flowers <strong>and</strong> newly set fruits. The<br />
disease may appear earlier if conditions are favourable. The developing young<br />
leaves show a whitish powdery mass, which causes <strong>the</strong>m to shrink <strong>and</strong><br />
defoliate. The disease also appears in <strong>the</strong> <strong>for</strong>m of white powdery spots on <strong>the</strong><br />
surface of <strong>the</strong> fruits <strong>and</strong> later covers <strong>the</strong> whole fruit surface. The spots turn into<br />
light brown to dark brown discolouration. The infected area becomes slightly<br />
raised <strong>and</strong> rough. Affected fruits ei<strong>the</strong>r drop off prematurely or become corky,<br />
cracked, misshapen <strong>and</strong> remain underdeveloped. Sometimes <strong>the</strong> whole crop is<br />
rendered unmarketable (see Plate 9).<br />
The mycelium remains external on <strong>the</strong> host with white, single, upright<br />
conidiophores. The fungus survives in <strong>the</strong> bud wood of <strong>the</strong> host or in some<br />
alternate hosts during <strong>the</strong> absence of ber flowers <strong>and</strong> fruits. Mehta (1950)<br />
reported that <strong>the</strong> mycelium over-winters <strong>and</strong> arises annually in <strong>the</strong> new growth.<br />
These become primary sources of infection. Air-borne spores act as a<br />
secondary source of infection. The disease is observed on both cultivated <strong>and</strong><br />
wild <strong>for</strong>ms of ber.<br />
6.7.1.1 Control<br />
The disease can be controlled by spraying Dinocap (0.2 % Karathane WP or<br />
0.1 % Karathane EC), 0.2 % Sulfex (Gupta et al., 1977, 1978; Yadav <strong>and</strong><br />
Singh, 1985; Singh et al., 1995), 0.2 % Carbendazim (Yadav et al., 1980;<br />
Singh <strong>and</strong> Sidhu, 1985) or Trideomorph (Singh et al., 1995). According to<br />
Kapoor et al. (1975) spray of 0.07 % Karathane EC or 0.3 % Sulfex achieved<br />
satisfactory control. Multi-location trials in India have shown that fungicides<br />
such as Dinocap (0.1 %), Carbendazim (0.1 %), wettable Sulphur (0.2 %),<br />
Trideomorph (0.1 %), Sulphur dust (250 g/tree) <strong>and</strong> Thiophenate Methyl<br />
(0.1 %) were effective <strong>for</strong> <strong>the</strong> control of powdery mildew. Sharma et al.<br />
71
(2001) evaluated Bayleton <strong>and</strong> Karathane sprays <strong>for</strong> control <strong>and</strong> both are<br />
effective but <strong>the</strong> <strong>for</strong>mer costs twice <strong>the</strong> latter. Starting with <strong>the</strong> initiation of <strong>the</strong><br />
disease, 2 to 4 sprays at 15-20 day intervals should be carried out depending<br />
upon disease intensity. The time of spray is critical <strong>for</strong> effective control. Gupta<br />
et al. (1978) <strong>and</strong> Singh <strong>and</strong> Sidhu (1985) suggested that spraying should be<br />
started as soon as <strong>the</strong> disease appears on fruits of peanut size <strong>and</strong> repeated at 3-<br />
week intervals. In regions with an established record of recurrence of <strong>the</strong><br />
disease, one spray of fungicide should be applied as a prophylactic measure as<br />
soon as growth appears after pruning (Pareek <strong>and</strong> Nath, 1996).<br />
6.7.1.2 Cultivars<br />
Although some cultivars have been reported to be resistant under field<br />
conditions (Jeyarajan <strong>and</strong> Cheema, 1972; Kapoor et al., 1975; Gupta et al.,<br />
1978; Lodha et al., 1984), <strong>the</strong> reaction of <strong>the</strong>se cultivars to <strong>the</strong> disease has<br />
varied at different locations <strong>and</strong> in different years. The disease affects several<br />
Ziziphus species <strong>and</strong> all <strong>the</strong> ber cultivars. <strong>Ber</strong> cultivars Illaichi Jhajjar, Gola,<br />
Seb, Safed Rohtak <strong>and</strong> Mehrun have shown comparative tolerance to <strong>the</strong><br />
disease in nor<strong>the</strong>rn India. Five local genotypes (Darakhi-1, Darakhi-2, Guli,<br />
Villaiti <strong>and</strong> Seedless) have been reported to be free from <strong>the</strong> disease. Umran<br />
S<strong>and</strong>hura, Narul, Iuaichia <strong>and</strong> Kaithli are susceptible. Safeda Rohtak is a recent<br />
cultivar selected <strong>for</strong> resistance to powdery mildew (Godhara et al., 2002). Wax<br />
levels of immature fruits <strong>and</strong> leaves play a role in degree of susceptibility<br />
(Pradeep <strong>and</strong> Jambhale, 2001).<br />
6.7.2 Alternaria leaf spot<br />
Several species of Alternaria cause this disease, e.g. Alternaria anomorph of<br />
Lewia (Pleospora) infectoria (Gupta <strong>and</strong> Madaan, 1977 a), Alternaria<br />
anomorph of Pleospora caricola, Pleospora passeriniana (Panwar <strong>and</strong> Vyas,<br />
1971), Alternaria sp. (Jeyarajan <strong>and</strong> Cheema, 1972), Alternaria chartarum<br />
(Rao, 1971), Alternaria tenuissima (Kanaujia <strong>and</strong> Kishore, 1977). In Ziziphus<br />
oenoplia, <strong>the</strong> disease is caused by Annellophorella (Chary <strong>and</strong> Ramarao, 1971).<br />
The disease caused by <strong>the</strong> Alternaria anomorph of Leiwa (Pleospora)<br />
infectoria, produces small, irregular brown spots on <strong>the</strong> upper surface of <strong>the</strong><br />
leaves <strong>and</strong> dark brown to black spots on <strong>the</strong> lower surface. The spots coalesce<br />
<strong>for</strong>ming large blighted patches <strong>and</strong> <strong>the</strong> affected leaves drop (see Plate 10).<br />
The disease develops at temperatures from 20 to 30 o C (Madaan <strong>and</strong> Ch<strong>and</strong>,<br />
1985), but high humidity <strong>and</strong> frequent rainfall appear to be more important.<br />
Plant debris seems to be a source of primary infection. Secondary infection is<br />
possibly caused by dissemination of spores under frequent rainfall.<br />
72
6.7.2.1 Control<br />
The disease can be controlled by spraying 0.3 % mancozeb or 0.2 % captafol or<br />
0.3 % copper oxychloride (Pareek <strong>and</strong> Nath, 1996). Gupta <strong>and</strong> Madaan, (1978)<br />
recommended a spray of 0.2 % difolatan or Dithane Z-78.<br />
6.7.2.2 Cultivars<br />
Jeyarajan <strong>and</strong> Cheema (1972) found all 35 ber cultivars tested to be susceptible<br />
to Alternaria leaf spot disease. Cultivars Govindgarh Special, Gola, Gurgaon,<br />
Popular Gola, Seo-Bahadirgarhia, ZG-3, Sofed Rohtak <strong>and</strong> Jhajjar Special were<br />
reported to be resistant by Gupta <strong>and</strong> Malaan, (1978, 1980).<br />
6.7.3 Black leaf spot<br />
This is caused by Isariopsis indica var. ziziphi <strong>and</strong> is also known as Isariopsis<br />
mouldy leaf spot (Gupta <strong>and</strong> Madaan, 1977 b). The disease has been observed<br />
under comparatively humid conditions. (see Plate 11)<br />
The disease is characterised by sooty tuft-like circular to irregular black spots<br />
on <strong>the</strong> underside of <strong>the</strong> leaves. Later, it covers <strong>the</strong> entire lower surface giving a<br />
sooty appearance. The leaves show yellowish <strong>and</strong> brownish discolouration on<br />
<strong>the</strong> upper surface <strong>and</strong> drop prematurely. The fungus survives in plant debris<br />
<strong>and</strong> soil, which are <strong>the</strong> primary sources of infection. Secondary infection is<br />
initiated from spores present in <strong>the</strong> air.<br />
6.7.3.1 Control<br />
The disease can be controlled by captafol (0.2 %), carbendazim (0.1 %),<br />
mancozeb (0.2 %) <strong>and</strong> copper oxychloride (0.2 %). The sprays should be<br />
applied 2-3 times at 15 day intervals starting with <strong>the</strong> first sign of symptoms<br />
(Pareek <strong>and</strong> Nath, 1996). Rawal <strong>and</strong> Saxena (1989) obtained good control by<br />
0.1 % carbendazim <strong>and</strong> 0.2 % chlorothalonil. Sharma et al. (1983) obtained<br />
best control by 0.3 % zineb or 0.6 % Blitox. Singh <strong>and</strong> Andotra (1989)<br />
controlled <strong>the</strong> disease by sprays of 0.1 % Bengard <strong>and</strong> thiophenate methyl.<br />
Ch<strong>and</strong> et al. (1986) recommended spraying 0.2 % carbendazim or captafol.<br />
Gupta <strong>and</strong> Madaan (1979) found a mycoparasite, Hans<strong>for</strong>dia pulvinata<br />
growing on <strong>the</strong> diseased spots which checked fur<strong>the</strong>r disease growth on <strong>the</strong><br />
host. More investigations are required on use of such biocontrol agents.<br />
6.7.3.2 Cultivars<br />
<strong>Ber</strong> cultivars Seo-Bahadurgarhia, ZG-3, Safed Rohtak <strong>and</strong> Sanaur-1 have been<br />
found to resist <strong>the</strong> disease infection in a multilocation trial in India (Pareek <strong>and</strong><br />
Nath, 1996). Cultivars Mundia, Banarsi Karaka, Banarsi Pew<strong>and</strong>i <strong>and</strong> Bagwadi<br />
also showed resistance to <strong>the</strong> disease at some locations.<br />
73
6.7.4 Cercospora leaf spot<br />
Cercospora ziziphae (Rao, 1962; Yadav, 1963a; Govindu <strong>and</strong> Thirumalachar,<br />
1964; Gupta <strong>and</strong> Madaan, 1975 b) <strong>and</strong> C. jujubae (Chona et al., 1959;<br />
Vasudeva, 1960; Agarwal <strong>and</strong> Sahni, 1964; Golsen <strong>and</strong> Rubin, 1964) infect<br />
ber, but <strong>the</strong> <strong>for</strong>mer is <strong>the</strong> most common <strong>and</strong> occurs during spring. The disease<br />
manifests itself in <strong>the</strong> <strong>for</strong>m of circular to oval spots, measuring up to 4 mm in<br />
diameter, epiphyllous, yellow at first <strong>and</strong> turning brown surrounded by a darkbrown<br />
margin. The spots grow larger <strong>and</strong> become visible on both sides of <strong>the</strong><br />
leaves. The infected leaves fall off.<br />
Cercospora leaf spot is also found on Chinese jujube, causing leaf yellowing.<br />
The fungus produces dark coloured stroma. It survives in debris <strong>and</strong> soil, <strong>the</strong><br />
primary sources of infection. The spores are disseminated by wind.<br />
6.7.4.1 Control<br />
The disease can be controlled by spraying 0.2 % Dithane Z-78 or Dithane M-<br />
45. Cultivars Safed Rohtak, ZG-3, Seo-Bahadurgarhia, Popular Gola, Rashmi<br />
<strong>and</strong> Jhajjar Selection were resistant to Cercospora (Ch<strong>and</strong> et al., 1986).<br />
6.7.5 Cladosporium leaf spot<br />
Cladosporium ziziphi (Uppal et al., 1935; Prasad <strong>and</strong> Verma, 1970; Saini <strong>and</strong><br />
Suppal, 1981) <strong>and</strong> C. herbarum (Gupta <strong>and</strong> Madaan, 1975b) cause this disease,<br />
with attacks occurring in <strong>the</strong> autumn.<br />
The symptoms appear in <strong>the</strong> <strong>for</strong>m of small, light brown to brown irregular<br />
spots on <strong>the</strong> lower surface of leaves. The disease starts on leaves closest to <strong>the</strong><br />
soil surface, where <strong>the</strong> fungus occurs. It is also spread by spores present in <strong>the</strong><br />
air. The fungal spores survive in plant debris <strong>and</strong> soil, <strong>the</strong> primary sources of<br />
infection.<br />
6.7.5.1 Control<br />
Two sprays of 0.2 % copper oxychloride or zineb or mancozeb should be<br />
applied at 2-week intervals (Pareek <strong>and</strong> Nath, 1996) starting from <strong>the</strong><br />
appearance of <strong>the</strong> symptoms.<br />
6.7.5.2 Cultivars<br />
Cultivars S<strong>and</strong>hura Narnaul <strong>and</strong> Jogia were found to be resistant. Ch<strong>and</strong> et al.<br />
(1986) observed that cultivars ZG-3, Banarsi, Govindgarh Selection-3, Jhajjar<br />
Selection <strong>and</strong> Jogia were also resistant.<br />
74
6.7.6 Rust<br />
Although rust can be serious in ber, it is less so in Chinese jujube (see Plate<br />
12).<br />
Rust is caused by Phakospora ziziphi-vulgaris (Sydow <strong>and</strong> Sydow, 1907;<br />
Yadav, 1963b; Gupta et al., 1984). The disease appears towards <strong>the</strong> end of<br />
winter on <strong>the</strong> leaves in <strong>the</strong> <strong>for</strong>m of small, irregular, reddish-brown<br />
uredopustules on <strong>the</strong> lower surface. Pustules aggregate on <strong>the</strong> tips <strong>and</strong> margins<br />
resulting in large necrotic spots <strong>and</strong> death of tissues. The infection advances<br />
over <strong>the</strong> whole surface <strong>and</strong> <strong>the</strong> infected leaves become dry <strong>and</strong> fall off.<br />
6.7.6.1 Control<br />
The disease can be controlled by application of 0.4 % copper oxychloride or<br />
0.2 % zineb or captafol (Pareek <strong>and</strong> Nath, 1996). In Chinese jujube, <strong>the</strong> disease<br />
severity was reduced by 84.9-97.5 % after application of metalaxyl <strong>and</strong><br />
Bordeaux mixture (Sun et al., 1989).<br />
6.7.6.2 Cultivars<br />
Ch<strong>and</strong> et al. (1986) reported cultivars Banarsi, Seo, Katha Gurgaon, Gola<br />
Gurgaon-2, D<strong>and</strong>an, Sanaur-1, Safeda Selected <strong>and</strong> Sanaur-3 to be resistant.<br />
Several <strong>o<strong>the</strong>r</strong> foliar pathogens have also been reported to infect ber (Appendix<br />
I).<br />
6.7.7 Witches’ broom<br />
Witches’ broom affects both Indian <strong>and</strong> Chinese jujubes (Kim, 1965; Zhu et<br />
al., 1983).<br />
P<strong>and</strong>ey et al. (1976) first reported <strong>the</strong> disease in ber. The affected trees become<br />
weak <strong>and</strong> produce small, yellow leaves typical of <strong>o<strong>the</strong>r</strong> phytoplasma diseases.<br />
The disease is transmitted to healthy seedlings by budding <strong>and</strong> graftingwith<br />
diseased scions.<br />
6.7.7.1 Control<br />
The disease can be contained by treatment with 500 <strong>and</strong> 1000 ppm<br />
oxytetracycline. La et al. (1977) recommended control through transfer of 1000<br />
ppm tetracycline hydrochloride into <strong>the</strong> trees from a plastic reservoir through<br />
plastic tubes. Wang et al. (1980) successfully controlled it by two commercial<br />
<strong>for</strong>mulations of oxytetracycline.<br />
6.7.8 Fruit rot<br />
Fruit rot is caused by Phoma hissarensis (Gupta <strong>and</strong> Madaan, 1975 a),<br />
Colletotrichum gloeosporioides (Gupta <strong>and</strong> Madaan, 1977 c), Tricho<strong>the</strong>cium<br />
roseum (Gupta <strong>and</strong> Madaan, 1977 c), Alternaria state of Pleospora infectoria<br />
75
(Ch<strong>and</strong> et al., 1986), Cladosporium hebarum <strong>and</strong> a number of minor<br />
pathogens. Sources of resistance have been looked <strong>for</strong> by Nallathambi et al.<br />
(2000).<br />
6.7.8.1 Phoma fruit rot<br />
The disease appears on <strong>the</strong> ripening fruit. The infected fruits remain small <strong>and</strong><br />
develop slightly depressed, dark brown spots near <strong>the</strong> stem ends. The lesions<br />
become irregular in shape <strong>and</strong> measure 15-25 mm in diameter.<br />
The fungus survives in plant debris, <strong>the</strong> primary source of infection. The<br />
disease can be controlled by spraying of 0.2 % Dithane Z-78 or Dithane M-45<br />
(Ch<strong>and</strong> et al., 1986).<br />
6.7.8.2 Alternaria fruit rot<br />
Slightly depressed, brown to dark brown, circular lesions appear on <strong>the</strong> fruit.<br />
Sometimes concentric rings are also present on <strong>the</strong>se spots. The smaller spots<br />
coalesce to <strong>for</strong>m larger spots. The fungus survives in debris <strong>and</strong> soil. The fruits<br />
touching <strong>the</strong> soil become infected <strong>and</strong> <strong>the</strong> disease spreads later by<br />
dissemination of spores through <strong>the</strong> air. The disease can be controlled by<br />
spraying of 0.2 % Dithane Z-78 (Ch<strong>and</strong> et al., 1986) (see Plate 13).<br />
6.7.8.3 Colletotrichum fruit rot<br />
The disease appears at <strong>the</strong> start of ripening of <strong>the</strong> fruit in <strong>the</strong> <strong>for</strong>m of small,<br />
slightly depressed, light brown, water-soaked lesions. These spots coalesce <strong>and</strong><br />
enlarge. Under humid conditions, <strong>the</strong> acervuli are <strong>for</strong>med in masses on <strong>the</strong>se<br />
spots.<br />
Being saprophytic <strong>the</strong> pathogen survives in soil, along with <strong>the</strong> debris, <strong>for</strong> a<br />
long period. This becomes <strong>the</strong> primary source of infection. The spores are<br />
present in <strong>the</strong> air <strong>and</strong> act as secondary sources of infection <strong>and</strong> are<br />
disseminated by rain splashes. The disease can be controlled by 2-3 sprays of<br />
0.2 % copper oxychloride at 3-weekly intervals (Ch<strong>and</strong> et al., 1986).<br />
6.7.8.4 Tricho<strong>the</strong>cium fruit rot<br />
The disease is observed during <strong>the</strong> spring in <strong>the</strong> <strong>for</strong>m of pink spots on <strong>the</strong><br />
fruits. The fungus can survive in <strong>the</strong> soil <strong>for</strong> a long time. Fruits touching <strong>the</strong><br />
soil may become infected <strong>and</strong> develop symptoms.<br />
6.7.8.5 Cladosporium fruit rot<br />
The disease appears near <strong>the</strong> time of fruit ripening. Injured fruits become<br />
infected. The symptoms of <strong>the</strong> disease start from <strong>the</strong> tip of <strong>the</strong> fruit <strong>for</strong>ming<br />
light brown to dark brown spots. Later, a greenish fungal growth is also seen on<br />
<strong>the</strong>se spots.<br />
76
6.7.8.6 O<strong>the</strong>r fruit rot fungi<br />
A range of minor fungal pathogens also cause fruit rot. They are listed by<br />
Ch<strong>and</strong> et al. (1986).<br />
6.7.9 Minor foliar pathogens<br />
A range of minor foliar pathogens affect leaves of ber. They are also listed by<br />
Ch<strong>and</strong> et al. (1986).<br />
6.8 Cropping systems<br />
Jujube species provide nutritious fruits at relatively low costs. Fruits are<br />
produced even under adverse agroclimatic conditions. Except <strong>for</strong> China,<br />
Vietnam <strong>and</strong> <strong>the</strong> Central Asian Republics jujubes are still produced under less<br />
intensive cropping systems, although more intensive orchards are increasing in<br />
India <strong>and</strong> Bangladesh.<br />
In many areas, especially with arid zones, <strong>the</strong>re is great interest in using<br />
Ziziphus species <strong>for</strong> hedging <strong>and</strong> enhanced local use at <strong>the</strong> smallholder level.<br />
This is being exp<strong>and</strong>ed, particularly in Africa, through agro<strong>for</strong>estry.<br />
Preliminary results obtained from provenance trials conducted in African<br />
countries under <strong>the</strong> Semi Arid Lowl<strong>and</strong>s of West Africa (SALWA) programme<br />
of <strong>the</strong> International Centre <strong>for</strong> Research on Agro<strong>for</strong>estry (ICRAF), have<br />
provided encouraging results. They show compatibility of ber within an<br />
agro<strong>for</strong>estry system <strong>and</strong> as a live fence along with <strong>o<strong>the</strong>r</strong> adapted tree species. In<br />
India, ber is one of <strong>the</strong> most suitable agro<strong>for</strong>estry trees in arid <strong>and</strong> semi-arid<br />
areas.<br />
In China intercropping is widespread <strong>and</strong> this is increasing in India also.<br />
At maturity, ber trees cover <strong>the</strong> entire inter-row spaces about five years after<br />
planting. In <strong>the</strong> meantime, considerable losses occur from vacant interspaces.<br />
By growing intercrops, <strong>the</strong> losses can be minimised <strong>and</strong> additional income<br />
generated. Intercrops such as mung bean, moth bean, cowpea, clusterbean <strong>and</strong><br />
sesame can be grown under rainfed conditions during <strong>the</strong> summer. The yields<br />
of both ber <strong>and</strong> <strong>the</strong> intercrops are higher than in monoculture <strong>and</strong> no adverse<br />
effects are observed <strong>for</strong> up to five years after planting <strong>the</strong> ber trees (Singh et<br />
al., 1997, Patel et al., 2003). Under irrigated conditions, horse gram, cumin,<br />
chillies <strong>and</strong> <strong>o<strong>the</strong>r</strong> vegetables are more profitable (Pareek, 1983). In <strong>the</strong> semiarid<br />
plateau of western India, a ber + clusterbean combination gave <strong>the</strong> highest<br />
net returns per hectare followed by ber + cowpea, ber + okra, <strong>and</strong> ber + brinjal<br />
combinations (Raturi <strong>and</strong> Chadha, 1993). Under arid <strong>and</strong> semi-arid conditions,<br />
strong competition has been observed by Khan (1993) between ber trees <strong>and</strong><br />
crops like wheat <strong>and</strong> chickpea. He suggested that <strong>the</strong> cost of keeping Ziziphus<br />
77
trees was more than <strong>the</strong> value <strong>for</strong>egone by growing <strong>the</strong>se crops. Thus, such<br />
crops should not be grown as intercrops in ber orchards (see Plate 14).<br />
Cover cropping with kulthi (Dolichos biflorus) was found to increase waterholding<br />
capacity of light soils as a result of increased organic carbon content in<br />
arid regions of <strong>the</strong> tropics (Pareek <strong>and</strong> Nath, 1996). The legume Stylosan<strong>the</strong>s<br />
hamata is a good cover crop in <strong>the</strong> semi-arid regions of western India (Raturi<br />
<strong>and</strong> Chadha, 1993).<br />
<strong>Ber</strong> trees fit very well into agro<strong>for</strong>estry systems when <strong>the</strong> companion species<br />
suited to <strong>the</strong> same agroclimatic conditions of <strong>the</strong> location are selected, e.g. <strong>the</strong><br />
leguminous tree, Prosopis cineraria, under <strong>the</strong> arid climate of northwest India.<br />
However, appropriate spacing <strong>and</strong> management systems should be used. Most<br />
of such systems will be locally developed, although where governments have a<br />
national institute or programme dedicated to agro<strong>for</strong>estry research, sharing of<br />
experiences at diverse local levels can be expected.<br />
78
7.1 Introduction<br />
Chapter 7. Breeding<br />
A. Godara<br />
Plant breeders look <strong>for</strong> ideal plant types or ideotypes, in addition to selection<br />
<strong>for</strong> yield <strong>and</strong> <strong>o<strong>the</strong>r</strong> screenable characters. The idea is to combine maximum<br />
desirable traits in a cultivar. Characters that are determined by a few genes with<br />
clear effect are much simpler <strong>and</strong> more effective to select than traits determined<br />
by <strong>the</strong> additive effects of many genes, each having limited individual effect.<br />
Table 7.1 shows <strong>the</strong> desirable <strong>for</strong>ms of some morphological traits as well as<br />
those <strong>for</strong> yield attributes in Indian jujube.<br />
Table 7.1 Ideotypes of ber<br />
Character Ideotype Character Ideotype<br />
Root system Deep (> 2 m) Fruit size > 30 g<br />
Canopy Spreading, low headed <strong>and</strong> TSS in pulp > 15 o Brix<br />
thornless<br />
Leaf area High Acidity in < 0.3%<br />
pulp<br />
Internodal Short (< 5 cm) Fruit shape Round to oval<br />
length<br />
Leaf colour Dark green (chlorophyll Fruit colour Bright golden<br />
> 0.04 mg/kg fresh wt.)<br />
Leaf surface Glossy dorsal <strong>and</strong> tomentose<br />
ventral<br />
Fruit surface Glossy <strong>and</strong><br />
smooth<br />
Leaf size Large (> 50 cm 2 ) Pulp/stone > 20<br />
ratio<br />
(Source: Pareek, 2001)<br />
The inflorescence consists of male <strong>and</strong> hermaphrodite flowers. It is highly<br />
heterozygous because of cross-pollination. The existence of polyploidy <strong>and</strong> a<br />
range of self <strong>and</strong> cross incompatibilities in Ziziphus species has resulted in<br />
wide hybridisation. Current ber cultivars have evolved through selection of<br />
superior types from <strong>the</strong> wide natural variability. Some of <strong>the</strong> selected<br />
genotypes received widespread popularity <strong>and</strong> became established as cultivars<br />
suitable <strong>for</strong> orchard planting, although cultivars tend to lack good quality, or<br />
high productivity <strong>and</strong> tolerance to biotic <strong>and</strong> abiotic stresses. There is a need to<br />
improve <strong>the</strong> crop <strong>for</strong> commercial cultivation in different agro-ecological<br />
environments.<br />
79
Various techniques of breeding can be grouped into broad headings viz.,<br />
introduction, selection, hybridisation, polyploidy, mutation, breeding,<br />
biotechnological methods <strong>and</strong> genetic engineering. Like any <strong>o<strong>the</strong>r</strong> crop <strong>the</strong>y<br />
have been widely used <strong>for</strong> improvement of tropical fruit crops. The<br />
investigations <strong>and</strong> breeding work required to develop Z. mauritiana <strong>and</strong> Z.<br />
jujuba into a commercial crop in Australia have been outlined (Possingham,<br />
1990). Most of this chapter relates to Indian jujube.<br />
7.2 Breeding objectives<br />
The breeding programme must have well defined objectives which are both<br />
economically <strong>and</strong> biologically reasonable. Despite wide cultivar diversity of<br />
<strong>the</strong> two major jujubes, only a few cultivars are commercially important. It<br />
appears that productivity along with ability to withst<strong>and</strong> transport <strong>and</strong> storage<br />
are <strong>the</strong> basic requirements in a cultivar. In addition, it should have high TSS,<br />
good sugar-acid blend, crisp flesh, <strong>and</strong> good flavour besides resistance to<br />
common insect pests <strong>and</strong> diseases. Earliness is a desirable trait in cultivars<br />
meant <strong>for</strong> dry, rainfed regions or to be grown under irrigated conditions. The<br />
objectives <strong>for</strong> <strong>the</strong> breeding of ber have been described by Chadha (1998) <strong>and</strong><br />
Ray (2002).<br />
So far, yield <strong>and</strong> fruit quality are <strong>the</strong> traits that have received <strong>the</strong> greatest<br />
emphasis in ber breeding. Precociousness, profuse bearing, attractive fruit<br />
colour, crispy pulp, firm texture, high soluble solids, good eating quality,<br />
smaller seed size, long shelf life, resistances to pests, diseases <strong>and</strong><br />
environmental stress have been <strong>o<strong>the</strong>r</strong> major objectives. Time of maturity is also<br />
an important characteristic to be considered. It is associated primarily with <strong>the</strong><br />
response of genotype to photoperiod <strong>and</strong> temperature. Selection <strong>for</strong> time of<br />
maturity is a major initial step in evaluating genotypes <strong>and</strong> <strong>the</strong> extent <strong>and</strong><br />
availability of variation among genotypes to h<strong>and</strong> greatly influence decision<br />
making. Limited variation in germplasm imposes restrictions. Setting <strong>the</strong><br />
objectives must also take account that specific traits have different inheritance<br />
patterns. Variation in inheritance pattern of different traits can complicate <strong>the</strong><br />
process of easy parent selection <strong>for</strong> crosses to be made.<br />
Resistance to diseases, particularly powdery mildew (Oidium erysiphoides f.<br />
ziziphi) <strong>and</strong> Isariopsis; pests, like fruitfly (Carpomyia vesuviana) <strong>and</strong> fruit<br />
borer (Meridarchis scyrodes); salt <strong>and</strong> low temperature tolerances, giving good<br />
fruit set under high temperature conditions; <strong>and</strong> fruits with better eating <strong>and</strong><br />
processing quality are major objectives <strong>for</strong> Z. mauritiana. Rootstocks suitable<br />
<strong>for</strong> high density orchards are also required. In Z. jujuba, resistance to cracking,<br />
disease resistance particularly JWB, <strong>and</strong> tolerance to high temperature are<br />
important. The present <strong>and</strong> future goals <strong>for</strong> cultivar improvement in China-<br />
Taiwan are presented <strong>for</strong> Z. mauritiana in preparation <strong>for</strong> World Trade<br />
Organization st<strong>and</strong>ards. The development of consumer orientated, small scale<br />
local <strong>and</strong> all year round producing cultivars is needed (Wang et al., 1997 a).<br />
80
7.3 Constraints/ bottlenecks in breeding<br />
<strong>Ber</strong> breeding is hampered by <strong>the</strong> long juvenile phase, high heterozygosity (<strong>and</strong><br />
cross-pollination), inadequate knowledge of inheritance patterns <strong>and</strong> well<br />
established pre-selection criteria of traits such as incompatibility patterns,<br />
sterility <strong>and</strong> fruit drop. The small size of flowers <strong>and</strong> <strong>the</strong>ir behaviour at an<strong>the</strong>sis<br />
dehiscence pose practical constraints in ber improvement.<br />
<strong>Ber</strong> shows ranges of polyploidy <strong>and</strong> incompatibilities in its cultivars (Pareek,<br />
1996). Most ber cultivars are tetraploids, showing much segregation.<br />
Accordingly, many cultivars have been reported to be reciprocally cross<br />
incompatible (Teaotia <strong>and</strong> Chauhan, 1963, 1964), while several cultivars<br />
including Umran are self incompatible (Godara, 1980). Godara (1980) showed<br />
cross compatibility in Illaichi x Kakrola Gola giving high seed set while <strong>the</strong><br />
crosses Kathaphal x Safeda Selected <strong>and</strong> Kaithali x Kakrola Gola were<br />
incompatible. Umran show <strong>the</strong> best combining ability with <strong>o<strong>the</strong>r</strong> cultivars<br />
when used as female or male. Fruit set under open pollination ranged from<br />
3.56% in ZG2 to 18.7% in Illaichi; Illaichi <strong>and</strong> Umran set fruit when flowers<br />
were bagged but ZG 2 <strong>and</strong> Sanaur 2 did not (Mehrotra <strong>and</strong> Gupta, 1985).<br />
7.4 Breeding methods<br />
Plant breeders need a range of germplasm carrying different desirable genes in<br />
order to combine such genes through recombination breeding. The acquisition<br />
of diverse <strong>and</strong> elite germplasm from exotic sources is an important activity in<br />
germplasm management.<br />
7.4.1 Selection<br />
Most of <strong>the</strong> cultivars of ber grown in tropical, subtropical <strong>and</strong> temperate<br />
regions of <strong>the</strong> world are straight<strong>for</strong>ward historical selections. Major emphasis<br />
has been put on clonal selection especially of early maturing clones. The local<br />
cultivars are <strong>the</strong> result of selection made by local people.<br />
Selection does not create genetic variability but merely acts on <strong>the</strong> genetic<br />
variability already available. Thus <strong>the</strong> breeder must first create a variable<br />
population through building up a collection of a large number of genotypes<br />
from different regions <strong>and</strong>/or countries. Selection is straight<strong>for</strong>ward in an<br />
asexually propagated crop since any genotype may be perpetuated intact;<br />
however, <strong>the</strong> measure of success is how to test <strong>for</strong> <strong>the</strong> most desirable<br />
genotypes. Obtaining segregating populations, from which superior genotypes<br />
may be found, is difficult in asexually propagated material. Un<strong>for</strong>tunately, <strong>the</strong><br />
most desirable selections do not always make <strong>the</strong> best parents; consequently,<br />
potential parents are best selected on <strong>the</strong> basis of progeny per<strong>for</strong>mance.<br />
81
A wide range of variability exists in ber in India <strong>for</strong> all important characters<br />
suggesting substantial scope <strong>for</strong> improvement. An early maturing clone, Early<br />
Umran (Pareek, 1996) has been identified from normally late maturing Umran.<br />
Promising cultivars under commercial cultivation are Gola, Seb, Banarsi<br />
Karaka, Banarsi Peondi, ZG-1, Sanour-1, 2,3,4, Kath, Umran, <strong>and</strong> Mundia.<br />
Gomakirti is a clonal selection from Umran which flowered 25 days earlier. A<br />
recent selection, CIAH Sel-1 developed by CIAH Bikaner, from local material<br />
collected from Bhusawar area of Rajasthan, is more juicy <strong>and</strong> sweet <strong>and</strong> is also<br />
an early bearer besides being resistant to fruit rot (Shukla et al., 2004).<br />
A clonal selection <strong>for</strong> earliness with quality fruits <strong>and</strong> better storage life with<br />
consistent productivity from Umran was identified at Central Horticultural<br />
Experiment Station, Godhara, <strong>and</strong> Gujarat, India. After evaluation trials, <strong>the</strong><br />
selection was found to be early compared to Umran, flowering three weeks<br />
earlier, <strong>and</strong> it matured with <strong>the</strong> early cultivar Gola. It has been released as<br />
Goma Kirti (Hiwale, 2005).<br />
The distribution <strong>and</strong> vegetative <strong>and</strong> fruiting characteristics of Z mauritiana<br />
trees in <strong>the</strong> Korean Republic were studied between 1968 <strong>and</strong> 1971. Thirty six<br />
strains scored high marks on a selection scale <strong>for</strong> disease resistance, high yield<br />
<strong>and</strong> fruit quality <strong>and</strong> five were selected <strong>for</strong> general use (Kim et al., 1980).<br />
Wonye-A-Ol was selected from 254 lines developed from Moodeung <strong>and</strong><br />
Geumsung (Kim et al., 1988). Gaolang 1 is a selection of Z. mauritiana from<br />
Taiwan (Chen et al., 2000). In Azerbaijan, Tagiev (1976) evaluated 3762<br />
seedlings. The best 40 were selected, of which 25 were included as elites. The<br />
eleven best <strong>for</strong>ms were given cultivar names: <strong>the</strong> major ones being Nasimi,<br />
Mardakyan, Akhmedi, Khazari <strong>and</strong> Irada. Two small fruited <strong>for</strong>ms were<br />
selected <strong>for</strong> use as rootstocks.<br />
Several attempts have been made in <strong>the</strong> recent past to select high yielding,<br />
better quality Z. mauritiana in China (Yu et al., 1991 <strong>and</strong> Zhu et al., 1998).<br />
Some of <strong>the</strong>se selections have been described: Lejin-1 <strong>and</strong> Lejin-2 (derived<br />
from Jinsixlao Zao) <strong>and</strong> Leling Seedless-1 (derived from Wahexiaozao or<br />
Seedless Xiaozao). All <strong>the</strong>se have larger fruits, better eating quality <strong>and</strong> higher<br />
resistance to fruit cracking. Six Chinese cultivars: Sovetskii, Tavrika,<br />
Tayantszao, Suontszao, Druzhba <strong>and</strong> Kitaiskii, have been reported to be<br />
promising in <strong>the</strong> Ukraine (Sin’ko <strong>and</strong> Litvinova, 1996). Recently five superior<br />
Russian cultivars (Yuzhanin, Khurman, Burnim, Kitaiskii-93 <strong>and</strong> Finik) have<br />
been registered (Kudenkov <strong>and</strong> Beloshtskaya, 1998). Cultivar Jinsixiaozao was<br />
closely related to Wuhexiaozao, Wuhexiaozao might have evolved from<br />
Jinsixiaozao, <strong>and</strong> Guangyangzao was closely related to Chuanganzao (Peng et<br />
al., 1996).<br />
Yanliang xiaozao is a cultivar selected from Lintong Chizao jujube orchards in<br />
Yanliang District, Xi’an, China (Li et al., 2004 a). Juzhou Gongzao is derived<br />
from a chance seedling (Ma et al., 2000). Cangwu 1 <strong>and</strong> Cangwu 3 are<br />
82
selections of Z. jujuba cv. seedless (Ji et al., 2001). Jiaxian Youzao was<br />
selected from Z. jujuba cv. Zhongyang Muzao orchards in Jiaxian country in<br />
Shaanxi, (Li et al., 2003). Qiyuexian was selected as a highly nutritious clone<br />
suitable <strong>for</strong> <strong>the</strong> production of table fruits in Heyang country, Shaanxi Province,<br />
(Wang et al., 2003). Two cultivars with good emergence were selected;<br />
Gissarskii Semennoi-3 (Gissar seed) <strong>and</strong> Gissarskii Semennoi-7, (Massover<br />
1976).<br />
7.4.2 Hybridisation<br />
Combining characters by sexual crossing is by far <strong>the</strong> most popular method <strong>for</strong><br />
obtaining plants that have more favourable combinations of desirable traits.<br />
When <strong>the</strong> characters are distributed in many cultivars, or <strong>the</strong> desirable<br />
characters are associated with many undesirable ones, <strong>the</strong> procedure requires<br />
many crosses <strong>and</strong> many generations. It has two main virtues: one is to increase<br />
<strong>the</strong> genetic variation in plants <strong>and</strong> <strong>the</strong>ir progenies <strong>and</strong> to keep <strong>the</strong> population<br />
stable, while <strong>the</strong> <strong>o<strong>the</strong>r</strong> is to increase plant vigour <strong>and</strong> thus make <strong>the</strong> plants or<br />
cultivar more able to compete with <strong>o<strong>the</strong>r</strong>s. Not all hybrid combinations result in<br />
above average vigour (heterosis) but commercially desirable types can be<br />
identified by suitable experimentation.<br />
In perennial fruit trees improvement through hybridisation requires several<br />
decades. For vegetatively propagated fruit crops <strong>the</strong> aim is a single desirable<br />
genotype. This genotype may be of any degree of heterozygosity with no<br />
problem of genetic maintenance due to asexual propagation. Asexually<br />
propagated crops are usually cross pollinated <strong>and</strong> consequently highly<br />
heterozygous, thus in developing populations from which to select a desirable<br />
genotype, inbreeding should be avoided. Unrelated plants are usually<br />
hybridised in order to obtain a vigorous population from which <strong>the</strong> most<br />
desirable individuals may be selected. Once a good genetic combination has<br />
been identified it can be propagated immediately as a new cultivar.<br />
In order to find superior hybrids with a wide range of fruit traits, as well as<br />
adaptation to diverse climates, several cultivars have been used in India as<br />
parents. Extensively used ones are Umran, Banarsi Karaka, Kakrola, Gola,<br />
Mundia Murhara, Sanori, Illaichi, Safeda Selected, Kaithali, Reshmi, Chhuhara<br />
<strong>and</strong> Seb. At Hisar, Umran <strong>and</strong> Banarsi Karaka were used <strong>for</strong> high yield, Gola<br />
<strong>for</strong> quality <strong>and</strong> earliness, Illaichi <strong>for</strong> profuse bearing, BS 7S-3 <strong>for</strong> drought <strong>and</strong><br />
fruit fly tolerance, Reshmi <strong>for</strong> fruit quality <strong>and</strong> Mundia Murhara <strong>and</strong> Kathaphal<br />
<strong>for</strong> attractive colour <strong>and</strong> fruit quality (softness). At Jodhpur, Katha was crossed<br />
with Seb <strong>and</strong> Seb with Tikadi (Pareek, 2001). At <strong>the</strong> CIAH Bikaner, CIAH<br />
hybrid 1 (Seb x Katha) was found to be a promising, precocious, prolific<br />
bearer, <strong>and</strong> early maturer with good fruit set at high temperature under arid<br />
conditions (Shukla et al., 2004). For fruit fly resistance BCF1 (Seb x Tikadi F 1<br />
x Seb) is under evaluation (Anon., 2002).<br />
83
Fruit setting of four Z. mauritiana cultivars (Umran, Karaka, Popular Gola <strong>and</strong><br />
Chhuhara) after pollination with powdery mildew resistant cultivars Villaiti,<br />
Darakhi 1, Darakhi 2 <strong>and</strong> Guli was observed. The best female parents were<br />
Umran <strong>and</strong> Gola, both setting fruit with each of <strong>the</strong> pollinators, whereas, <strong>the</strong><br />
best male parent was Darakhi 2, setting fruit with each of <strong>the</strong> female cultivars<br />
(Karale et al., 1992).<br />
Hybridisation to evolve superior quality, high yielding, early <strong>and</strong> drought<br />
tolerant cultivars was taken up at Hisar, <strong>and</strong> <strong>for</strong> inducing long shelf life <strong>and</strong><br />
resistance to fruit fly at Jodhpur. Evaluation of hybrids is in progress.<br />
The cultivar Seb was crossed with a local cultivar, Tikadi, resistant to fruit fly<br />
(Carpomyia vesuviana) in order to develop a pest resistant cultivar. The F1 was<br />
90 % resistant, but had poor fruit quality. By backcrossing to Seb, a BCI line<br />
with 87-90 % resistance <strong>and</strong> desirable fruit characters was obtained. A mean of<br />
13 % fruit fly infestation was observed in this line, along with a high level of<br />
antibiosis. Fruits weighed around 16 g (4.5 g in <strong>the</strong> F1) <strong>and</strong> Brix value was 24 0<br />
(Faroda, 1996).<br />
By crossing large fruited introduced Z. jujuba cultivars Tayan-tszao,<br />
Dardomskii, Yubilainyi with a local small fruited <strong>for</strong>m, diverse new material<br />
was produced in Azerbaizhan. These exhibited large fruit <strong>and</strong> good flavour,<br />
high yield <strong>and</strong> disease resistance, including <strong>the</strong> variety Khurman (bred using<br />
Tayan-tszao). This had large fruits weighing 15-17 g, with an acid sweet<br />
flavour, a thin skin <strong>and</strong> tender flesh (Akhundova <strong>and</strong> Agaev, 1989).<br />
More in<strong>for</strong>mation is needed on <strong>the</strong> relationship between Z. jujuba <strong>and</strong> Z.<br />
mauritiana, on <strong>the</strong> possibility of hybridising <strong>the</strong> two groups, on <strong>the</strong> chilling<br />
requirement of Z. jujuba <strong>and</strong> <strong>the</strong> frost tolerance of Z. mauritiana. Although<br />
Meyer (1911) travelled widely in China more than 60 years ago <strong>and</strong> introduced<br />
many of <strong>the</strong> <strong>the</strong>n best cultivars to <strong>the</strong> USA, <strong>the</strong>re are probably <strong>o<strong>the</strong>r</strong>s that<br />
would be of value in USA. Meyer mentioned a ‘seedless jujube cultivar: Wuhu<br />
tsao had a kernel so soft that it is almost imperceptible when eaten’. He was<br />
told that this was <strong>the</strong> only seedless cultivar in China. Meyer also mentioned<br />
several flat-fruited jujubes, a white-fruited jujube <strong>and</strong> <strong>the</strong> quaint ‘dragon's<br />
claw’ jujube, which had peculiar gnarled <strong>and</strong> twisted branches <strong>and</strong> was<br />
cultivated as an ornamental (Meyer, 1911). India may also have jujubes that<br />
would be useful in USA. The US Department of Agriculture initiated a jujube<br />
breeding programme at Chico, Cali<strong>for</strong>nia in 1952 but this was terminated about<br />
1959 (Ackerman, 1961).<br />
7.4.3 Mutation<br />
Changes in individual genes or whole chromosomes introduce new heritable<br />
characters known as mutations. Mutations provide a valuable source of<br />
variation in plant material from which <strong>the</strong> breeder can make selections. In<br />
84
nature, gene mutation occurs at a very low frequency, but <strong>the</strong> rate can be<br />
speeded up <strong>and</strong> mutation can be induced artificially by ionizing radiation, nonionising<br />
radiation, <strong>and</strong> by treating with chemical mutagens such as ethyl<br />
methane sulphonate, diethyl sulphate, nitroso-compounds (nitrous acid),<br />
nucleoside analogues <strong>and</strong> sodium azide. Since a number of useful alterations<br />
have been accomplished by means of induced mutations, it has been tried<br />
successfully in many fruit crops. Mutated shoots or <strong>o<strong>the</strong>r</strong> parts can usually be<br />
propagated readily after recognition of a desired mutation. This makes it<br />
possible to improve one or a few characters of leading cultivars without<br />
changing <strong>the</strong> remaining, unique, genotype.<br />
The heterozygosity of most vegetatively propagated plants is an<strong>o<strong>the</strong>r</strong> cause of<br />
increasing application of mutation breeding to <strong>the</strong>m. In such plants mutations,<br />
from dominant to recessive, can be observed in <strong>the</strong> irradiated material itself,<br />
especially when easily selectable characters (<strong>for</strong>m, colour, size) are concerned<br />
(Broertjes, 1968).<br />
The use of spontaneous mutants with an improved agronomic or horticultural<br />
value is probably as old as agriculture itself. Most early examples, often<br />
outlined in extensive reports, refer to so-called bud mutations in vegetatively<br />
propagated crops such as fruit trees, ornamentals etc. (Darwin, 1868; Shamel<br />
<strong>and</strong> Pomeroy, 1936). Somatic mutations of spontaneous origin within<br />
vegetatively propagated material are commonly referred to as sports. Desirable<br />
mutations occurring in adapted, asexually propagated plants may result in an<br />
immediate improvement. Tainung No.1, a bud sport of Kaolung No.1, was<br />
found in Pintung, Taiwan (Chang et. al., 2001). Thereafter, <strong>the</strong> Fengshan<br />
Tropical Horticultural Experiment Station conducted a stability evaluation on<br />
this new selected mutation cultivar in 1992 <strong>and</strong> 1993, <strong>and</strong> confirmed that this<br />
new cultivar was a hereditary cultivar. Luyuan Xiaozao is a sport of Xiaozao<br />
discovered in 1990 in Zhangjiapo, Yiyuan country, China (Li et al., 1996).<br />
Mutations that occur in somatic tissue may be confined to only a sector of<br />
tissue, resulting in a chimera. Such chimeras, when vegetatively propagated,<br />
tend to be unstable because buds may be <strong>for</strong>med from tissue with or without<br />
<strong>the</strong> mutation. The selection of desirable sports is an important means of<br />
improving asexually propagated crops.<br />
Artificially-induced mutation has been used. The highest induction with<br />
colchicine treatment (0.15 %/18 h) was 50 % in cv. Linyilizao <strong>and</strong> 43.3 % in<br />
Dongzao <strong>and</strong> Lajiaozao reported by Jiang <strong>and</strong> Liu (2004). The chromosome<br />
number of <strong>the</strong> mutated plants (2n = 4x = 44) <strong>and</strong> DNA content were both twice<br />
that of <strong>the</strong> control. Useful mutants have also been produced by gamma<br />
irradiation <strong>and</strong> colchicine treatment in Z. jujuba (Akhundova <strong>and</strong> Agaev,<br />
1989). Variation in seedlings of Z. jujuba after treatment with ethyeneimine,<br />
ethyl methanesulphonate, dimethyl sulphate; <strong>and</strong> gamma radiation was<br />
observed <strong>and</strong> some propagated vegetatively <strong>for</strong> fur<strong>the</strong>r trials (Sin’ko <strong>and</strong><br />
85
Chemarin, 1979 b, 1982). Sin’ko <strong>and</strong> Chemarin (1979 a) reported on seeds of<br />
Z. jujuba irradiated at 0.1 to 100 Krad some 60-98 % germination obtained<br />
from seeds treated with low doses (0.5-2.0 Krad). The 30 Krad dose was<br />
critical. The treatment had no effect on <strong>the</strong> rate of emergence. Treatment with<br />
0.5-5 Krad stimulated seedling growth, development of lateral shoots <strong>and</strong> root<br />
length <strong>and</strong> advanced cropping whereas higher doses inhibited <strong>the</strong>se processes.<br />
Colchicine <strong>and</strong> ethyl methanesulphonate treatments of Z. mauritiana increased<br />
crossability <strong>and</strong> reduced premature fruit drop (Gupta <strong>and</strong> Minhas, 1991).<br />
Gamma irradiation resulted in high fruit set.<br />
Mutants selected following N-methyl-N-nitrosourea treatment (0.02-0.04 % <strong>for</strong><br />
12 h) of pregerminated seeds of Ziziphus mauritiana cultivars included cultivar<br />
Ma Hong, which maintains <strong>the</strong> early maturity of its parental cultivars, Gia Loc,<br />
allowing two harvests per year. Fruits, however, are round ra<strong>the</strong>r than oval,<br />
pink ra<strong>the</strong>r than yellow <strong>and</strong> sweet ra<strong>the</strong>r than sour. Also released is Dao Tien,<br />
which produces round fruits which are larger (25 vs. 20 g) with better flavour<br />
than those of its parental cultivar, Thien Phien. It also is one month earlier in<br />
maturity, allowing two harvests/year ra<strong>the</strong>r than <strong>the</strong> one produced by Thien<br />
Phien (Hoang <strong>and</strong> Tuynh, 1989). Sin’ko <strong>and</strong> Chemarin (1979 b) studied <strong>the</strong><br />
seeds of four cultivars treated with various concentrations of ethylene imine,<br />
ethyl methanesulphonate <strong>and</strong> dimethyl sulphate. Some morphological changes<br />
induced in <strong>the</strong> first year, which included shortened internodes <strong>and</strong> altered leaf<br />
shape <strong>and</strong> size, were retained in subsequent years. Treatment tended to delay<br />
flowering, especially in Nikitskii-58, but increased precocity, with numerous<br />
seedlings fruiting in <strong>the</strong> third year.<br />
7.4.4 Polyploidy<br />
An<strong>o<strong>the</strong>r</strong> technique <strong>for</strong> improvement is exploitation of polyploidy; <strong>the</strong> condition<br />
of chromosome duplication giving numbers of chromosomes over <strong>and</strong> above<br />
<strong>the</strong> basic duplicate number. Unless <strong>the</strong> number of chromosomes is an exact<br />
multiple of <strong>the</strong> diploid, <strong>the</strong> polyploid is unstable <strong>and</strong> gives rise to gametes with<br />
irregular numbers of chromosomes. Gametes with irregular numbers may<br />
combine in a <strong>for</strong>tuitous manner however, to give rise to a polyploid with even<br />
chromosome numbers (a multiple of <strong>the</strong> diploid), <strong>and</strong> plants from <strong>the</strong> newly<br />
<strong>for</strong>med seeds may <strong>the</strong>n be fully fertile. Any sterility results from <strong>the</strong> inability of<br />
chromosomes to pair at meiosis; fertility is restored by doubling <strong>the</strong><br />
chromosome number of <strong>the</strong> sterile hybrid or by crossing autotetraploids of each<br />
species.<br />
Polyploidy may be important in conferring desirable characteristics. Polyploidy<br />
may be artificially induced by using colchicine at a concentration of 0.05 to 0.3<br />
per cent. Induced polyploidy makes it possible to overcome sterility associated<br />
with interspecific hybrids.<br />
86
Transfer of powdery mildew resistance from diploid genotypes of Ziziphus to<br />
tetraploid cultivars required doubling of chromosomes in resistant genotypes in<br />
order to overcome <strong>the</strong> possible post-fertilisation barrier. Attempts have been<br />
made to induce polyploidy in some of <strong>the</strong> resistant diploid genotypes of<br />
Ziziphus that were confirmed cytologically (Pradeep <strong>and</strong> Jambhale, 2003).<br />
The behaviour at meiosis e.g. bivalents <strong>and</strong> quadrivalents can show some<br />
cultivars of Z. mauritiana are cytologically alloploid (Pradeep <strong>and</strong> Jambhab,<br />
2002). The numbers of stomata <strong>and</strong> chloroplasts in diploid, tetraploid,<br />
pentaploid <strong>and</strong> octaploid Z. mauritiana genotypes indicate significant<br />
differences in stomatal dimensions, frequency of <strong>the</strong>ir occurrence <strong>and</strong><br />
chloroplast number per two stomatal guard cells among <strong>the</strong> different ploidy<br />
levels. However, no significant differences were observed between pentaploid<br />
<strong>and</strong> octoploid genotypes <strong>for</strong> <strong>the</strong>se attributes, indicating <strong>the</strong> deleterious effects<br />
of high gene dose beyond <strong>the</strong> pentaploid level (Pradeep <strong>and</strong> Jambhale, 2000).<br />
In a triploid Z. jujuba (Z. sativa) cultivar <strong>the</strong> water saturation deficit,<br />
transpiration rate <strong>and</strong> daily maximum transpiration rate were lower than two<br />
diploid cultivars (Wan, 1994).<br />
7.4.5 Biotechnological methods<br />
7.4.5.1 Tissue culture<br />
Tissue culture is one of <strong>the</strong> most widely used techniques <strong>for</strong> rapid asexual in<br />
vitro propagation. This technique is economical in time <strong>and</strong> space, af<strong>for</strong>ds<br />
greater output, <strong>and</strong> provides disease free <strong>and</strong> elite propagules. It also facilitates<br />
safer movements of germplasm between nations.<br />
Protocols have been developed <strong>for</strong> clonal propagation of Z. nummularia <strong>and</strong> Z.<br />
mauritiana (Rathore et al., 1992) <strong>and</strong> of Z. jujuba (Zhao et al., 2001). Methods<br />
<strong>for</strong> rapid in vitro multiplication of ber using stem explants of mature trees have<br />
been developed (Yan et al., 1990; Mathur et al., 1995). Benzyladenine<br />
promoted bud differentiation <strong>and</strong> IBA promoted root growth when added to<br />
MS medium on which stem segments of Z. jujuba lines A17, A27 <strong>and</strong> A80<br />
were cultured (Yan et al., 1990). Gola <strong>and</strong> Seb cultivars of Z. mauritiana take<br />
150 days from initial culturing to transplanting (Goyal <strong>and</strong> Arya, 1985).<br />
The present taxonomic systems of ber <strong>and</strong> Chinese jujube are based mainly on<br />
morphological characters, utilisation or distribution, which cannot accurately<br />
reflect <strong>the</strong> genetic relationship <strong>and</strong> result in serious nomenclature problems.<br />
This situation has hindered <strong>the</strong> scientific exploitation, germplasm conservation<br />
<strong>and</strong> academic exchange of jujubes. Use of molecular markers can facilitate<br />
proper identification of genotypes <strong>and</strong> help to overcome <strong>the</strong> problem of<br />
duplicity in genebanks. Raja (2004) looked at <strong>the</strong> technique to identify 12 ber<br />
genotypes at Hisar, India <strong>for</strong> categorisation <strong>and</strong> identification by molecular<br />
markers. DNA finger printing is used to identify genes resistant to biotic <strong>and</strong><br />
87
abiotic stresses. Such research deserves <strong>the</strong> attention of scientists <strong>and</strong> need to<br />
be initiated on priority.<br />
A protocol was developed <strong>for</strong> RAPD analysis of Z. jujuba Zanhuangdazao;<br />
Zanxindazao clones <strong>and</strong> a total of 70 b<strong>and</strong>s were amplified where 19 (27.14 %)<br />
were polymorphic (Zhao <strong>and</strong> Liu, 2003). Jiang et al. (2004) st<strong>and</strong>ardised tubeshoot<br />
multiplication in Z. jujuba var. sihongensis. A medium of direct<br />
regeneration of seedlings from stem fragments of jujube has been reported by<br />
Chen et al. (2005) <strong>and</strong> Wu et al. (2004). Z. jujuba buds <strong>and</strong> stem with side buds<br />
culturing in media MS + 6 – BA (4 mg litre -1 ) + IBA (0.3-0.4 mg litre -1 )<br />
produced 100 % of regeneration of adventitious buds <strong>and</strong> 4.15-4.19 fold<br />
proliferation (Wang et al., 2002).<br />
7.4.5.2 Genetic engineering<br />
Genetic engineering involves three major steps: identification <strong>and</strong> isolation of<br />
suitable genes <strong>for</strong> transfer; a delivery system to insert desired genes into<br />
recipient cells; <strong>and</strong> an expression of new genetic in<strong>for</strong>mation in recipient cells.<br />
Transgenic Chinese jujube plants have been obtained using young stems<br />
precultured <strong>for</strong> one day <strong>and</strong> infected with Agrobacterium tumefaciens which<br />
contained <strong>the</strong> anti-ACC synthase gene (He, 2004 b).<br />
7.4.5.3 Molecular markers<br />
The possibilities of using gene tags or molecular markers <strong>for</strong> selecting<br />
agronomic traits have made <strong>the</strong> job of <strong>the</strong> breeder easier. It has been possible to<br />
score <strong>the</strong> plants <strong>for</strong> different traits e.g. disease resistance, at <strong>the</strong> seedling stage<br />
itself. The uses of RFLP (Restriction Fragment Length polymorphism), RAPD<br />
(R<strong>and</strong>om Amplified Polymorphic DNA), AFLP (Amplified Fragment Length<br />
Polymorphism) <strong>and</strong> isozyme markers in plant breeding are numerous.<br />
The genetic relationship between 27 cultivar strains, <strong>and</strong> related species (Z.<br />
acidojujuba <strong>and</strong>, Z. mauritiana) of Z. jujuba were studied using r<strong>and</strong>om<br />
amplified polymorphic DNA (RAPD) technique by Lui et al. (2003). They<br />
reported a total of 92 DNA b<strong>and</strong>s were amplified with 15 primers screened<br />
from 80 arbitrary 10-mer primers, 77 of which (83.7 %) were polymorphic<br />
beside. RAPD fingerprint of 11 excellent strains of Zanhuangdazao were<br />
established using five primers. The S154-780 bp b<strong>and</strong> was regarded as a<br />
molecular marker linked to <strong>the</strong> stoneless character according to <strong>the</strong> study of 17<br />
samples of two closely related groups viz., Jinsixiaozao (with stones) <strong>and</strong><br />
Wuhexiaozao (without stones).<br />
The DNA based marker systems, namely, r<strong>and</strong>om amplified polymorphic DNA<br />
(RAPD) <strong>and</strong> restriction fragment length polymorphism (RFLP) have been used<br />
in ber. RAPD analysis of germplasm resources on Chinese jujube has also been<br />
reported by Peng et al. (2000). Genomic DNA was isolated from leaves of Z.<br />
mauritiana suitable <strong>for</strong> RAPD analysis without liquid nitrogen, making it<br />
advantageous over <strong>o<strong>the</strong>r</strong> common protocols (Sharma et al., 2003). Polymerase<br />
88
chain reaction-restriction fragment length polymorphism (PCR-RFLP) can be<br />
used to determine <strong>the</strong> relationships among <strong>the</strong> phytoplasms infecting various<br />
woody host species. Amplification of <strong>the</strong> DNA with primers specific to <strong>the</strong> 16S<br />
rRNA gene generated a 1.4 kb b<strong>and</strong> in Z. jujuba (Han et al., 1996). Ziziphus<br />
jujuba has been reported to be infected with phytoplasms in Korea. Isolation<br />
<strong>and</strong> PCR amplification of genomic DNA from Ziziphus nummularia has been<br />
reported by Shukla et al. (2000).<br />
7.4.5.4 Embryo rescue<br />
Embryo rescue is an<strong>o<strong>the</strong>r</strong> area where plant breeders are able to rescue <strong>the</strong>ir<br />
crosses which would <strong>o<strong>the</strong>r</strong>wise abort. Culture of excised embryos at suitable<br />
stages of development can circumvent problems encountered in post zygotic<br />
incompatibility. This technique is highly significant in intractable <strong>and</strong> long<br />
duration horticultural species.<br />
Most cultivars of Chinese jujube have very serious embryo abortion (Qi <strong>and</strong><br />
Liu, 2004). Liu <strong>and</strong> Qi (2004) established an optimised system <strong>for</strong> embryo<br />
culture in order to get hybrids of four excellent cultivars Dongzao, Jisifeng,<br />
Wudeng, <strong>and</strong> Fuzao. Embryo rescue techniques may help developing hybrids<br />
of suitable combination in Indian ber especially in sterile <strong>and</strong> incompatible<br />
cultivars. Plant regeneration by somatic embryogenesis has been attempted<br />
successfully in Chinese jujube by Mitrofanova et al. (1997).<br />
7.4.5.5 In vitro screening<br />
The flower number per fruit branch, pollen number, time of an<strong>the</strong>r dehiscence,<br />
pollen germination percentage, pollen vigour <strong>and</strong> storage of pollen collected at<br />
different stages of flowering in Z. jujuba <strong>and</strong> var. spinosa, have been studied in<br />
vitro by Liu et al. (2004b). The two taxa varied in flower number per fruit<br />
branch, pollen number <strong>and</strong> pollen germination percentage <strong>and</strong> <strong>the</strong>se parameters<br />
were grouped in three grades by probability grading <strong>for</strong> quantitative characters.<br />
The time of an<strong>the</strong>r dehiscence in both <strong>the</strong> species was at <strong>the</strong> yellow bud stage<br />
or bud breaking stage. The pollen germination percentage after storage showed<br />
a drop-rise-drop tendency.<br />
7.4.6 Current situation<br />
The enormous variability in Z. mauritiana <strong>and</strong> Z. jujuba <strong>and</strong> related species has<br />
been inadequately exploited. Most breeding work has been done in India <strong>and</strong><br />
China. There is tremendous scope <strong>for</strong> using improved methods.<br />
<strong>Ber</strong> has attracted sustained breeding attention owing to its wide adaptability,<br />
good quality <strong>and</strong> nutritive fruits. However, problems like poor shelf life,<br />
powdery mildew disease, fruit fly <strong>and</strong> fruit borer have hindered <strong>the</strong> extension<br />
of <strong>the</strong> area under this crop. In Chinese jujube <strong>the</strong> problem of fruit cracking <strong>and</strong><br />
jujube witches broom disease are <strong>the</strong> major hindrances to be addressed.<br />
89
Thus <strong>the</strong> following priorities are identified <strong>for</strong>:<br />
<br />
<br />
<br />
<br />
<br />
Systematic collection, characterization of germplasm <strong>and</strong><br />
identification of cultivars with desirable traits.<br />
Study of patterns of inheritance of many qualitative characters.<br />
Breeding <strong>for</strong> cultivars to suit different agroclimatic conditions.<br />
Development of resistance to biotic <strong>and</strong> abiotic factors including fruit<br />
cracking.<br />
Development of quality cultivars with attractive golden yellow colour<br />
<strong>and</strong> good keeping quality.<br />
90
Chapter 8. Genetic Resources<br />
A. Godara<br />
8.1 The Ziziphus genepool<br />
Chapter 1 pointed out that <strong>the</strong> two major cultivated species are widely<br />
distributed in suitable climates in Asia <strong>and</strong> <strong>the</strong>y cover vast regions. Most of<br />
<strong>the</strong>se distributions comprise wild or naturalised materials superimposed on <strong>the</strong><br />
patterns of distribution in <strong>the</strong> areas where <strong>the</strong> species are cultivated.<br />
The wild populations are heterozygous <strong>and</strong> extremely variable <strong>and</strong> it is from<br />
<strong>the</strong>se that farmers have selected <strong>the</strong> best trees in terms of production <strong>and</strong><br />
propagated <strong>the</strong>m vegetatively, but are now doing so more <strong>and</strong> more through<br />
grafting. Indian jujube is not easily propagated through cuttings but Chinese<br />
jujube is. A study of wild populations of Chinese jujube has identified<br />
promising types to use as germplasm (Liu <strong>and</strong> Wang, 1991).<br />
As a result of <strong>the</strong> millennia of local selection many cultivars arose, some of<br />
which have become widely recognised.<br />
None<strong>the</strong>less, virtually nothing is known about <strong>the</strong> patterns of genetic variation<br />
in <strong>the</strong> wild populations of any of <strong>the</strong> <strong>o<strong>the</strong>r</strong> cultivated species of jujube. Nor has<br />
<strong>the</strong>re been much research on identifying <strong>the</strong> traits of <strong>the</strong> large number of<br />
Ziziphus species. What little is known will be apparent from <strong>the</strong> following<br />
sections of this chapter.<br />
8.1.1 Chromosome numbers<br />
A good number of chromosome counts have been made <strong>for</strong> <strong>the</strong> two major<br />
cultivated jujubes. The counts are not always easy to interpret because a range<br />
of synonyms were used <strong>for</strong> <strong>the</strong> taxa investigated <strong>and</strong> without voucher<br />
specimens some counts can be interpreted differently. However, it appears that<br />
Indian jujube is usually polyploidy with counts of n = 12, 20, 24, 30, 36, or 48.<br />
Khoshoo <strong>and</strong> Singh (1963) looked at a range of cultivars <strong>and</strong> found n = 24 in<br />
most, but in two it was n = 48 <strong>and</strong> in one it was n = 30. In some wild material.<br />
Nehra et al. (1983) found n = 48; <strong>and</strong> also in naturalised ‘wild’ material it was<br />
<strong>the</strong> same count.<br />
Not too many wild species have been counted but from <strong>the</strong> few that have<br />
(particularly Z. lotus, Z. nummularia <strong>and</strong> Z. oenoplia), n = 10, 12, or 36. Z.<br />
lotus appears to be diploid, Z. oenoplia tetraploid <strong>and</strong> Z. nummularia shows a<br />
polyploid series. The possibility exists that <strong>the</strong> genus is tribasic with x = 10, 12,<br />
or 13 (Darlington <strong>and</strong> Wylie, 1955).<br />
91
It is now generally thought that Indian jujube shows a range of polyploids:<br />
diploid, triploid, tetraploid, pentaploid <strong>and</strong> octoploid (Mehetre <strong>and</strong> Dahat,<br />
2000). Chinese jujube also represents a polyploid series, chromosome counts<br />
tending to represent 2n = 45, 60, 90.<br />
The phylogenetic relationship between <strong>the</strong> two major species (Z. mauritiana<br />
<strong>and</strong> Z. jujuba) has not been worked out nor has <strong>the</strong>ir cross compatibility been<br />
investigated. Chinese jujube exhibited high diversity in chromosome<br />
karyotypes, shape, size <strong>and</strong> surface sculpture of pollen, leaf length <strong>and</strong> flower<br />
diameter, shape, colour, weight of fruit, growth period <strong>and</strong> soluble solids <strong>and</strong><br />
ascorbic acid of fruits.<br />
The level of ploidy appears to be important <strong>for</strong> some cultivars of Indian jujube.<br />
Tekale (1997) noted that powdery mildew resistant genotypes were diploids<br />
<strong>and</strong> a seedless <strong>for</strong>m was octoploid. However, <strong>o<strong>the</strong>r</strong> diploid cultivars were<br />
susceptible to powdery mildew.<br />
More focused research is needed to see whe<strong>the</strong>r cytology relates to specific<br />
patterns of adaptation or to <strong>o<strong>the</strong>r</strong> types of variation, especially in wild<br />
materials. Knowledge of basic cytology is needed to plan introgression from<br />
wild species or <strong>for</strong> planning a crossing programme.<br />
8.1.2 Hybridisation<br />
The taxonomic literature on Ziziphus refers to reputed hybrids between certain<br />
wild species. It is highly likely that a number of <strong>the</strong> taxa generally accepted<br />
will turn out to be stabilised hybrid segregates. Fur<strong>the</strong>r insight into this could<br />
be useful in relation to genetic resources <strong>for</strong> use in breeding.<br />
In practice, improvement programmes have not yet successfully used<br />
hybridisation with wild species, although such interspecific hybridisation<br />
would be of potential value to exp<strong>and</strong> adaptation of cultivars to wider<br />
ecological areas <strong>and</strong> to introduce resistances to pests <strong>and</strong> diseases.<br />
In Indian jujube <strong>the</strong>re in a long juvenile period <strong>and</strong> as with any woody<br />
perennial this poses constraints. Additionally, in both major cultivated jujubes<br />
<strong>the</strong> flowers are very small <strong>and</strong> <strong>the</strong> procedures <strong>for</strong> making crosses are delicate.<br />
For hybridisation between cultivars, constraints may arise due to some being<br />
incompatible with <strong>o<strong>the</strong>r</strong>s <strong>and</strong> <strong>the</strong> presence of polyploidy; again emphasising <strong>the</strong><br />
need <strong>for</strong> more cytological investigation.<br />
A number of <strong>the</strong> constraints can be overcome by <strong>the</strong> use of tissue culture,<br />
particularly <strong>for</strong> rapid propagation <strong>and</strong> overcoming <strong>the</strong> need to wait <strong>for</strong> seasonal<br />
growth. Use of shoot tips of Indian jujube is now practicable (Sudherson et al.,<br />
2001; Hu et al,. 2001; Mathur et al., 1993). For Chinese jujube see Kim <strong>and</strong><br />
92
Lee, 1988; Metrofonova <strong>and</strong> Shevelukha 1995; Zhao et al., 2001; Liu <strong>and</strong> Qi,<br />
2004).<br />
8.2 Cultivars<br />
The majority of cultivars of both Indian <strong>and</strong> Chinese jujubes are selections<br />
from heterogeneous populations. Superior genotypes had been protected <strong>and</strong><br />
used over millennia by local people so that location specific cultivars are<br />
widespread. Those that are used nowadays tend to be propagated clonally <strong>and</strong><br />
some have become very widespread e.g. Umran in Indian jujube; or Sui Men or<br />
Li in Chinese jujube.<br />
The cultivated ber has more than 300 varieties but only a few are commercially<br />
important (Pareek <strong>and</strong> Nath, 1996). Over 180 named cultivars have been<br />
mentioned in <strong>the</strong> literature (Pareek, 2001). Numerous cultivars have been<br />
selected during a long period. A Chinese work published over 300 years ago<br />
listed 43 cultivars (Locke, 1948). In China, <strong>the</strong>re are at least 400 cultivars of<br />
Chinese jujube (Hayes, 1945) but Qu <strong>and</strong> Wang, (1993) have reported more<br />
than 700 cultivars. These can be divided into two groups: <strong>the</strong> sour type mainly<br />
used as rootstocks, medicines or animal fodder, <strong>and</strong> <strong>the</strong> cultivated type<br />
(Ciminata, 1996). In<strong>for</strong>mation on genetic resources of Z. jujuba in Tongyu<br />
county, Jilin province, China has been given by Wang et al. (1999 b).<br />
8.2.1 Morphological variability <strong>and</strong> characterisation<br />
A wide variation due to cross pollination is exhibited by <strong>the</strong> jujubes in<br />
vegetative, leaf, floral, fruit <strong>and</strong> quality traits. Variation in morphological <strong>and</strong><br />
physicochemical characters of ber cultivated types have been reported by<br />
Shobha et al. (2001) <strong>and</strong> many <strong>o<strong>the</strong>r</strong>s. Details of <strong>the</strong> morphological variability<br />
in ber are provided below in order to illustrate constraints in attempting to<br />
classify cultivars <strong>and</strong> to sort out descriptors <strong>for</strong> characterisation.<br />
8.2.1.1 Variations in vegetative characters<br />
The most appropriate vegetative characters <strong>for</strong> classification are leaf area <strong>and</strong><br />
branching habit, while <strong>the</strong> most dependable fruit characters are apex type, stalk<br />
<strong>and</strong> stylar flesh cavities <strong>and</strong> shape (Bal, 1992). Ziziphus mauritiana genotypes<br />
Umran, Illaichi, Desi-1 <strong>and</strong> Desi-3 plants have a spreading habit, whereas,<br />
Kathapal <strong>and</strong> Desi-2 plants exhibit a semi-spreading habit. The cultivars of<br />
Gola group (Gola Gurgaon No. 3, Bhadurgarhia Gola, Dankan Gola, <strong>and</strong><br />
Kakrola Gola) produce erect plants (Gupta et al., 2003).<br />
Leaf margins of some cultivated <strong>and</strong> wild <strong>for</strong>ms of ber variously referred to as<br />
Z. mauritiana, Z. rotundifolia or Z. nummularia are serrated except in Desi-3<br />
<strong>and</strong> Jharber as reported by Gupta et al. (2003). Chitkara <strong>and</strong> Khera (1973)<br />
evaluated 15 varieties <strong>for</strong> leaf area. The product of maximum leaf length x<br />
breadth had a highly significant positive correlation with planimeter<br />
93
measurement of leaf area. The varieties may be classified into three groups,<br />
according to <strong>the</strong> percentage variation around <strong>the</strong> planimeter values. A nondestructive<br />
method of determining leaf area using linear parameter has been<br />
described (Hiwale <strong>and</strong> Raturi, 1991). The minimum stomatal density,<br />
internodal length <strong>and</strong> plant height were recorded in Gola budded onto Z.<br />
nummularia <strong>and</strong> was found to be <strong>the</strong> most dwarfing combination. Whereas,<br />
scion combination of Ponda budded onto rootstock Z. mauritiana ecotype-<br />
Assam-Gauhati was found <strong>the</strong> most vigorous, <strong>and</strong> <strong>the</strong> maximum stomatal<br />
density, internodal length <strong>and</strong> plant height were observed. The rootstock Z.<br />
mauritiana ecotype-291 was found most compatible <strong>and</strong> moderate in plant<br />
growth, stomatal density <strong>and</strong> internodal length <strong>the</strong>reby giving moderate vigour<br />
to trees (Verma et al., 2001).<br />
A range of variability in leaf size, shape, area <strong>and</strong> colour of 50 cultivars of Z.<br />
mauritiana can be seen in Plate 15. The list of cultivars is:<br />
1. Banarsi Karaka; 2. BS-75-1; 3. BS-75-2; 4. BS-75-3; 5. Chhuhara; 6.<br />
Chonchal; 7. D<strong>and</strong>an; 8. Desi; 9. Gola; 10. Gola Gurgaon No. 2; 11. Gola<br />
Gurgaon No. 3; 12. Golar, 13. Gora; 14. Govindgarh Special; 15. Hsiang Taso;<br />
16. Hsiang Tsao Chinese; 17. Hybrid G 1; 18. Illaichi; 19. Illaichi Jhajjar; 20.<br />
Jhajjar Special; 21. Jogia; 22. Jullundhari; 23. Kaithali;, 24. Kakrola Gola; 25.<br />
Katha Gurgaon; 26. Katha Rajasthan; 27. Kathaphal; 28. Kishmish; 29. Laddu;<br />
30. Mirchia; 31. Mundia Murhara; 32. Nari Kali; 33. Narma; 34. Noki; 35.<br />
Pathan; 36. Ponda; 37. Popular Gola; 38. Rashmi; 39. Safeda Rohtak; 40.<br />
Safeda Selected; 41. S<strong>and</strong>hura Narnaul; 42. Sanori No. 1; 43. Sanori No. 3; 44.<br />
Sanori No. 5; 45. Seo; 46. Seo Bhadurgarhia; 47. Sua; 48. Tasbtaro; 49.<br />
Thornless; 50. Triloki No. 1.<br />
Metroglyph <strong>and</strong> index score analysis showed wide morphological variation in<br />
80 germplasm accessions of Z. mauritiana <strong>and</strong> eight distinct groups were<br />
recognised on <strong>the</strong> basis of variation in 23 morphological <strong>and</strong> fruit characters<br />
(Pradeep <strong>and</strong> Jambhale, 2002). Paired spines were observed in many cultivars<br />
of Z. mauritiana like Umran, Kathaphal, Gola Gurgaon No. 3, Bhadurgarhia<br />
Gola, Dankan Gola <strong>and</strong> Kakrola Gola (Gupta et al,. 2003).<br />
8.2.1.2 Variations in growth characters<br />
Variation in <strong>the</strong> height (cv. Gola tallest <strong>and</strong> Akola shortest), spread (cv. Akola<br />
maximum spread) <strong>and</strong> branching nature was found in different cultivars at<br />
Hyderabad, India (Babu <strong>and</strong> Kumar, 1988). The maximum tree height was<br />
recorded in Desi Alwar while tree spread was in Sanori No.5 (Saran, 2005).<br />
Maximum height of a 15 year old tree of Z. mauritiana was recorded in LR-13<br />
(6.59 m); girth was maximum (3.32 m) in LR 11 (Kundi et al., 1989a). Data on<br />
growth of different species including Z. mauritiana at <strong>the</strong> International Centre<br />
<strong>for</strong> Research in Agro<strong>for</strong>estry, Machakos, Kenya (a sub-humid to semi-arid<br />
climatic zone) have been presented by Jama et al. (1989).<br />
94
8.2.2 Reproductive variability<br />
8.2.2.1 Flowering<br />
The peak period of flowering <strong>and</strong> fruit set in Z. mauritiana cultivars Banarsi<br />
Karaka, Ponda, Illaichi, Gola <strong>and</strong> Tikdi was September-October. Tikadi had <strong>the</strong><br />
shortest duration of flowering (47 days) <strong>and</strong> fruit set (36 days) but <strong>the</strong> highest<br />
number of fruits/branch (239), fruit set (28 %), number of fruits reaching<br />
maturity/branch (48) <strong>and</strong> fruit retention (20 %) (Sharma et al., 1990). Whereas,<br />
Saran (2005) found <strong>the</strong> longest period of bloom in Katha Rajasthan (78 days)<br />
ranged from 6 August to 23 October <strong>and</strong> <strong>the</strong> minimum period of bloom in <strong>the</strong><br />
Safeda Rohtak (23 days). Flowering occurred from 57 to 75 days, depending on<br />
cultivar (Dhaliwal <strong>and</strong> Bal, 1998). Only one flowering season was observed in<br />
Hyderabad from May to July <strong>and</strong> its total duration varied from 68-94 days.<br />
Cultivars Gola, Mundia <strong>and</strong> Akola flowered early; Umran <strong>and</strong> Seb in midseason;<br />
Banarsi <strong>and</strong> Kaki were late flowering (Babu <strong>and</strong> Kumar, 1988). The<br />
number of flowers per branch is quite high. Umran had <strong>the</strong> highest number of<br />
hermaphrodite flowers (22.2 %) followed by Gola Gurgaon with 20.1 %<br />
(Darbara <strong>and</strong> Jindal, 1982). Cultivars of Z. mauritiana differed in <strong>the</strong> time of<br />
flowering (on set <strong>and</strong> duration <strong>and</strong> peak) in Maharastra, India (Desai et al.,<br />
1986) (see Plates 16, 17).<br />
Healthy trees of Chinese jujube tend to produce a prodigious number of flowers<br />
<strong>and</strong> set of only a small fraction of <strong>the</strong>se is necessary <strong>for</strong> a substantial crop<br />
(Ackerman, 1961). Variation in flower number per fruit branch <strong>and</strong> pollen<br />
number in Z. jujuba <strong>and</strong> Z. spinosa were studied in vitro by Liu et al. (2004 b).<br />
The pollen of ber varieties has three zonicolporate aperture, psilate exine<br />
pattern <strong>and</strong> circular endocolpium. The pollen grains were sub-prolate to prolate<br />
spheroidal. Pollen germination was more than 50 per cent in most of <strong>the</strong> ber<br />
cultivars in 25 per cent sucrose solution whereas Illaichi cultivar was found to<br />
be sterile. The wild as well as cultivated ber types are tetraploid to octaploid.<br />
Scanning electron microscopic (SEM) <strong>and</strong> light microscopic studies were<br />
carried out on pollen samples of three Ziziphus species <strong>and</strong> six Z. mauritiana<br />
varieties. Pollen grains differed in size, shape <strong>and</strong> exine characteristics. Studies<br />
showed uni<strong>for</strong>mity in apertural characteristics <strong>and</strong> presence of tricolporate<br />
pollen. Size <strong>and</strong> shape of pollen within cultivars were quite uni<strong>for</strong>m.<br />
Differences in exine pattern, size <strong>and</strong> P/E ratios could be used <strong>for</strong> identification<br />
of Ziziphus genotypes (Diwakar et al., 1996).<br />
Size of pollen grains of Z. mauritiana Illaichi, Umran <strong>and</strong> four wild <strong>for</strong>ms was<br />
different (Nehra et al., 1984). Pollen diameter in seven cultivars of ber<br />
(Ziziphus mauritiana) ranged from 20.05 mμ in Darakhi 1 to 32.04 mμ in<br />
Seedless. Pollen stain ability ranged from 63.69 % in Seedless to 87.12 % in<br />
Darakhi 1. In vitro germination was a better indicator of fertility than <strong>the</strong> stain<br />
test (Hulwale et al., 1995). Similarly, considerable differences were also<br />
95
observed <strong>for</strong> pollen diameter among <strong>the</strong> different ploidy levels (Pradeep <strong>and</strong><br />
Jambhale, 2000). Phenetic relationships among 32 genotypes of Ziziphus<br />
mauritiana <strong>and</strong> one of Z. nummularia were studied using data on 54 characters<br />
<strong>and</strong> summarised in <strong>the</strong> <strong>for</strong>m of dendrograms. Overall, Z. nummularia did not<br />
show a close similarity to any of <strong>the</strong> Z. mauritiana genotypes (Diwakar et al.,<br />
1992).<br />
Studies in India have indicated that in Z. mauritiana, some cultivars have cross<br />
incompatibility (Teaotia <strong>and</strong> Chauhan, 1964). Ackerman (1961) showed many<br />
jujube cultivars fruit poorly without cross pollination. An<strong>o<strong>the</strong>r</strong> problem with<br />
jujube is that <strong>the</strong> fruit of some cultivars tends to split during rainy wea<strong>the</strong>r. The<br />
best time <strong>for</strong> pollen collection in crossbreeding has been discussed by Liu et al.<br />
(2004 b).<br />
8.2.2.2 Fruit set<br />
Umran was compatible as female parent with Sanuar 2, but Sanaur 2 did not set<br />
fruit after pollination by Umran (Mehrotra <strong>and</strong> Gupta, 1985). The requirement<br />
<strong>for</strong> cross pollination, incompatibility <strong>and</strong> pollen sterility means that fruit set<br />
depends on physiological <strong>and</strong> environmental conditions. The mode <strong>and</strong> time of<br />
an<strong>the</strong>sis was also cultivar specific. An<strong>the</strong>r dehiscence started about two hours<br />
after an<strong>the</strong>sis <strong>and</strong> continued <strong>for</strong> two to four hours. Peak receptivity of <strong>the</strong><br />
stigma appeared to be just as <strong>the</strong> flower opened (Dhaliwal <strong>and</strong> Bal, 1998).<br />
Some Chinese jujube clones developed fruits through self fertilization but few<br />
set appreciable crops by this means <strong>and</strong> fruits developed from self pollination<br />
were usually smaller than normal <strong>and</strong> tended to drop prematurely. Cross<br />
fertilisation was found necessary <strong>for</strong> <strong>the</strong> development of viable seeds <strong>and</strong> many<br />
of <strong>the</strong> aborted seeds apparently were <strong>the</strong> result of self fertilisation (Ackerman,<br />
1961).<br />
Fruit set in Z. mauritiana cultivars took place almost at <strong>the</strong> same time in<br />
Tikadi, Gola, Seb, Umran <strong>and</strong> <strong>the</strong> hybrid Umran x Seb cultivars, but Gola fruits<br />
matured earlier than those of all <strong>o<strong>the</strong>r</strong> cultivars in <strong>the</strong> region. Neeraja et al.<br />
(1995) reported higher fruit set in h<strong>and</strong> pollination than open pollination <strong>and</strong> 60<br />
% fruit set was observed in Umran X Seb.<br />
In Chinese jujube, fruit set was uni<strong>for</strong>mly high in Ya <strong>and</strong> Nikitskii<br />
Melkoplodnyi (Sin’ko, 1974a). Yakobashvili (1973) in a six year study of fruit<br />
set, yield <strong>and</strong> <strong>o<strong>the</strong>r</strong> characters, showed <strong>the</strong> following were promising varieties:<br />
Ta Yan Tszao, Seedling 2, Seedling 1 <strong>and</strong> 3.<br />
Fruit drop studied in seven Z. mauritiana cultivars indicated <strong>the</strong> lowest drop<br />
(24.1 %) in Ponda <strong>and</strong> highest in Illaichi (68.6 %) (Vashishtha <strong>and</strong> Pareek,<br />
1979). Kakrola Gola had considerably higher drop (up to 80.6 %) than Kaithali<br />
<strong>and</strong> Umran which did not differ significantly, showing 7.2 <strong>and</strong> 12.1 % drop,<br />
respectively (Panwar, 1980). More than 50 % of <strong>the</strong> drop was of fruit
diameter. As fruit development advanced, less fruit drop occurred. Neeraja et<br />
al. (1995) recorded <strong>the</strong> highest in Seb (87.94 %) followed by Umran (83.43 %)<br />
<strong>and</strong> Gola (82.14 %).<br />
The bearing <strong>and</strong> related characters provide useful in<strong>for</strong>mation on proper times<br />
of flower <strong>and</strong> fruit set <strong>and</strong> harvesting <strong>for</strong> <strong>the</strong> categorisation of ber varieties<br />
(Singh et al.,1972 b). Fruit maturity in different cultivars of Z. mauritiana was<br />
reached in 174 to 200 days (Kumar et al., 1986). Gola was <strong>the</strong> earliest (108<br />
days) <strong>and</strong> Umran was <strong>the</strong> latest (147 days) to ripen under Gurgaon conditions<br />
(Singh et al., 1983 a). Fruit growth in length <strong>and</strong> diameter showed three distinct<br />
phases (double sigmoid curve) in cultivar ZG-2 <strong>and</strong> Kaithali studied by<br />
Jaw<strong>and</strong>a <strong>and</strong> Bal (1980). Bal (1981 b) studied <strong>the</strong> physical character of ber fruit<br />
of six year old plants of cultivar Sanur-2. The fruit ripened 180 days after fruit<br />
set. There was a rapid growth phase up to 75 days, from 90 to 105 days <strong>and</strong><br />
from <strong>the</strong> 120 th day after fruit set. Maturity of ber (Z. mauritiana) starts from <strong>the</strong><br />
first week of November in South India <strong>and</strong> continues up to mid April in North<br />
India.<br />
Variation in maturity period of ber (Z. mauritiana) in different parts of India<br />
has been indicated by Vishal et al. (2002). Saran et al. (2005) studied <strong>the</strong><br />
bearing behaviour in 35 cultivars of ber at Hisar, India <strong>and</strong> classified <strong>the</strong>m into<br />
three categories based on harvesting time, as early, medium <strong>and</strong> late. Umran,<br />
Katha Bombay, Chhuhara, Illaichi, 2g-3, Kathaphal, Jogia, Ponda, BS-2 <strong>and</strong><br />
Desi Alwar are late bearing varieties while Gola, Gola Gurgaon No. 2, Gola<br />
Gurgaon No.3, Safeda Rohtak, Seo, Katha Rajasthan, Laddu <strong>and</strong> Akhrota were<br />
early bearing varieties <strong>and</strong> Kaithali, D<strong>and</strong>an <strong>and</strong> Mirchia varieties bear during<br />
<strong>the</strong> mid-season. Daulta <strong>and</strong> Chauhan, (1982) also observed that Umran is late<br />
<strong>and</strong> has large, oval, golden yellow fruits which turn chocolate brown at<br />
maturity <strong>and</strong> transport well. Kathaphal is late ripening while Gola is early <strong>and</strong><br />
Kaithali comes in midseason. Seo, Sanaur No.2 <strong>and</strong> Umran are recommended<br />
as early, mid <strong>and</strong> late cultivars, respectively <strong>for</strong> commercial cultivation<br />
(Chadha et al., 1972) in nor<strong>the</strong>rn India.<br />
8.2.2.3 Fruit <strong>and</strong> seed<br />
High variability was observed <strong>for</strong> all fruit <strong>and</strong> seed characters (Bisla <strong>and</strong><br />
Daulta, 1988 b). The variability of fruits of Z mauritiana is shown in Plates 26<br />
<strong>and</strong> 27. Considerable variation in fruit length <strong>and</strong> breadth in different cultivars<br />
of Z. mauritiana like Banarsi Karaka (5.4 <strong>and</strong> 3.4 cm), D<strong>and</strong>an (5.1 <strong>and</strong> 3.0<br />
cm), Jogia (4.9 <strong>and</strong> 3.8 cm) <strong>and</strong> Umran (4.8 <strong>and</strong> 3.8 cm) was reported by<br />
Ghosh <strong>and</strong> Ma<strong>the</strong>w (2002). Karaka had <strong>the</strong> largest fruit (Singh <strong>and</strong> Singh,<br />
1973). Fruit size, weight <strong>and</strong> pulp/stone ratio were highest in Umran (Dhingra<br />
et al., 1973). Fruit characters of 40 Z. mauritiana cultivars have been described<br />
by Singh et al. (1972 a) <strong>and</strong> variations in nine cultivars were described by<br />
Teaotia et al. (1974). Cultivars Seo Bahadurgarhia, Nari Keli, Desi Alwar <strong>and</strong><br />
Banarsi Karaka produced fruits weighing > 20 g each (Godara, 1980). Umran<br />
produced <strong>the</strong> heaviest fruits (39.8 g), Gola Gurgaon showed <strong>the</strong> highest content<br />
97
of pulp (97.2%), total soluble solids in Gurgaon, Haryana (Singh <strong>and</strong> Jindal,<br />
1980). The fruit weighed 70-90 g <strong>and</strong> reaches even 150 g in Wugianzhong, a Z.<br />
mauritiana cultivar (Li et al., 1999) (see Plates 18-25).<br />
The average fruit weight varied from 8 to 17.68 g in 10 local ber genotypes<br />
grown in West Bengal (Ghosh <strong>and</strong> Mitra, 2004). Nine varieties were evaluated<br />
by Teaotia et al. (1974). Pew<strong>and</strong>i was considered to be <strong>the</strong> best variety <strong>for</strong><br />
commercial cultivation, having <strong>the</strong> largest fruit, a high percentage of edible<br />
pulp <strong>and</strong> good skin colour. There were considerable differences in seven ber<br />
cultivars in fruit weight (29.340 to 9.544 g), fruit size (length 3.27-4.33 cm),<br />
pulp/seed ratio <strong>and</strong> fruit quality at Ratta Kulachi, D. I. Khan, Pakistan (Kundi<br />
et al , 1989b). BS-2 had <strong>the</strong> highest pulp/stone ratio; <strong>and</strong> <strong>the</strong> maximum fruit<br />
<strong>and</strong> stone size was recorded in Ponda (Saran, 2005). Cultivars Dabailing,<br />
Daguazao <strong>and</strong> Linyi Lizao are large fruited, with fruit sizes of 23-26.1 g, Jinsi<br />
3 <strong>and</strong> Jinsi 4 are small fruited varieties (Chen et al., 2003).<br />
The best Ziziphus jujuba varieties <strong>for</strong> uni<strong>for</strong>mity of fruit size are Ta-Pai <strong>and</strong><br />
Hsueh-pai (Sin’ko, 1974).<br />
A lot of variation exists in ber genotypes <strong>for</strong> pulp/stone ratio. Pulp/stone ratio<br />
was maximum in Sanur-6 <strong>and</strong> minimum in Punjab Chhuhara (Bharad et al.,<br />
2002), The pulp/stone ratio was highest in Umran (Dhingra et al., 1973).<br />
Madalageri et al. (1977) reported <strong>the</strong> highest pulp/stone ratio in HB-2, a wild<br />
local strain of Z. mauritiana.<br />
The list of cultivars as shown in Plates 26 <strong>and</strong> 27 is:<br />
1. Kaithali; 2. Umran; 3. Chonchal; 4. Noki; 5. Katha Rajasthan; 6. Laddu; 7.<br />
Chhuhara; 8. S<strong>and</strong>ura Narnaul; 9. Illaichi; 10. D<strong>and</strong>an; 11. ZG-3; 12. Kantha<br />
Phal; 13. Akhrota; 14. Bahaduragarhia; 15. Govindgarh Selection; 16.<br />
Thornless; 17. Gola Gurgaon No. 3; 18. Gola Gurgaon No. 2; 19. Desi Alwar;<br />
20. Nari Kali; 21. Gora; 22. Narina; 23. Sanori No. 5; 24. Sanori No. 1; 25. Seo<br />
Bahadurgarh; 26. Illaichi Jhajjar; 27. Sua; 28. Kishmish; 29. Popular Gola; 30.<br />
Mirchia; 31. Jogia; 32. Mundia Murhara; 33. Ponda; 34. Bawal Selection-2; 35.<br />
Gola; 36. Banarasi Karaka.<br />
Significant genotypic differences were found in <strong>the</strong> seed characters of Z.<br />
mauritiana varieties (Babu <strong>and</strong> Kumar, 1986). Saran (2005) observed variation<br />
in stone size of 35 cultivars of ber <strong>and</strong> reported that maximum (3.72 cm) was in<br />
Ponda <strong>and</strong> <strong>the</strong> minimum (0.53 cm) in Illaichi.<br />
Seeds of Ziziphus mauritiana trees taken from 5 districts in Yunnan Province,<br />
China <strong>and</strong> Narkum, Myanmar, were tested <strong>for</strong> <strong>the</strong>ir morphological<br />
characteristics, germination characteristics, <strong>and</strong> <strong>the</strong> growth patterns of <strong>the</strong><br />
seedlings <strong>and</strong> young trees. A close relationship was found between <strong>the</strong>se<br />
characters <strong>and</strong> <strong>the</strong>ir geographical distribution <strong>and</strong> climatic condition. This<br />
98
in<strong>for</strong>mation will be helpful <strong>for</strong> choosing better <strong>for</strong>ms of <strong>the</strong> tree (Wang <strong>and</strong><br />
Wang, 1994).<br />
In Chinese jujube, one group of cultivars gives 85 % seed germination (e.g. Yatszao)<br />
<strong>and</strong> <strong>the</strong> <strong>o<strong>the</strong>r</strong> gives 98 % germination, e.g. Nikitskii 84, 92 <strong>and</strong> 94. The<br />
results on seed germination with <strong>and</strong> without <strong>the</strong> endocarp in temperatures<br />
ranging from 15 to 30 o C are also presented (Sin’ko, 1973). Similarly, some<br />
Chinese jujube seeds take one to three days to germinate while <strong>o<strong>the</strong>r</strong>s take<br />
seven days (Kim <strong>and</strong> Kim, 1984a). Seed stones collected from fallen fruits of<br />
ber often have poor viability <strong>and</strong> 50 –70 % of <strong>the</strong> seed stones have non-viable<br />
seeds. The quickness <strong>and</strong> extent of germination depends upon viability <strong>and</strong><br />
after-ripening status of <strong>the</strong> seed, presence of endogenous inhibitors, wea<strong>the</strong>ring<br />
of <strong>the</strong> stony endocarp <strong>and</strong> environmental conditions such as <strong>the</strong> temperature,<br />
moisture, salinity <strong>and</strong> alkalinity of <strong>the</strong> growing medium. The thinnest seed coat<br />
wall was observed in <strong>the</strong> case of Godhan (Singh, et al., 1973 a).<br />
8.2.3 Yield<br />
Variation in yields of Z. mauritiana cultivars (55.5 to 116.11 kg/tree) have<br />
been observed by Kumar et al. (1986). In <strong>the</strong> semi-arid subtropical climate of<br />
nor<strong>the</strong>rn India under irrigated conditions, <strong>the</strong> fruit yield per tree ranges from 80<br />
to 200 kg depending on <strong>the</strong> varieties <strong>and</strong> management practices during <strong>the</strong><br />
prime bearing age of 10 to 20 years (Bakhshi <strong>and</strong> Singh, 1974). Fruit yield was<br />
highest in Gola (38.4 kg/tree) <strong>and</strong> lowest in <strong>the</strong> local cultivar Sukavani (3.54<br />
kg/tree) at Sardar Krushinagar in Gujarat (Chovatia et al. 1992). Highest yields<br />
were obtained from Umran (210 kg/tree) followed by Sanaur No. 2, D<strong>and</strong>an<br />
<strong>and</strong> ZG 2 (Gupta, 1977). Thornless gave <strong>the</strong> highest yield/tree (74.4 kg)<br />
followed by Sanaur 5 (71.3 kg) <strong>and</strong> Sanaur 4 (Singh <strong>and</strong> Tomar, 1988) at<br />
Bhatinda, Punjab, India. Kharki had <strong>the</strong> highest fruit yield at Hoshangabad,<br />
Madhya Pradesh (Gupta <strong>and</strong> Mehta, 2000).<br />
At Hyderabad, Mundia was <strong>the</strong> highest yielder (116.1 kg/tree) followed by<br />
Umran <strong>and</strong> Gola (s <strong>and</strong> Babu, 1987) whereas, yield in different cultivars of Z.<br />
mauritiana in Maharashtra (India) indicated maximum fruit, pulp <strong>and</strong> stone<br />
weights in Kadaka when pruned on 25 March (Bharad et al., 2002). Banarasi<br />
Karaka fruits had <strong>the</strong> highest nutritive value <strong>and</strong> yield (99.8 kg fruits/tree)<br />
(Tiwari <strong>and</strong> Banafar, 1995). Reddy et al. (1998) carried out an economic<br />
analysis of cost <strong>and</strong> returns to determine <strong>the</strong> most profitable cultivars at<br />
Dharwad, Karnataka, India. The per<strong>for</strong>mance of 11 cultivars showed that<br />
D<strong>and</strong>an, Sanaur-2 <strong>and</strong> Chhuhara, with mean fruit yields of 6.78, 6.36 <strong>and</strong> 6.08<br />
t/ha <strong>and</strong> benefit: cost ratios of 5.64, 5.32 <strong>and</strong> 5.09, respectively were <strong>the</strong> most<br />
promising. Cultivar Pew<strong>and</strong>i is considered best <strong>for</strong> commercial cultivation in<br />
Uttar Pradesh, India (Teaotia et al., 1974).<br />
Chinese jujube cultivars yield 50 to 300 kg fruits per year depending upon<br />
cultivar, location <strong>and</strong> age of tree (Ciminata, 1996). On <strong>the</strong> basis of yield,<br />
99
ipening date, frost resistance <strong>and</strong> storage quality in 7 ber cultivars Ta-Yantszao,<br />
Da-bai tszao, Ya-tszao, 93, 58, 107, 52 <strong>and</strong> 48 are recommended <strong>for</strong><br />
cultivation (Sin’ko, 1977). In <strong>the</strong> Arava valley of Israel, a fruit yield of 12 tons<br />
per hectare has been obtained from 3-year old ber trees (Nerd <strong>and</strong> Mizrahi,<br />
1998). From <strong>the</strong> naturally growing, scattered wild trees in Zimbabwe, a yield of<br />
4-5 tons has been obtained from a 3-4 hectare area (Maposa <strong>and</strong> Chisuro,<br />
1998). In China - Taiwan, fruit yields of 158.6 kg per tree in cultivar Kaolang-1<br />
<strong>and</strong> 140.8 kg per tree in cultivar Telong have been obtained (Chiv Chu Ying,<br />
1997).<br />
8.2.4 Chemical variability<br />
A wide range of varietal variability <strong>for</strong> quality traits was detected in 30<br />
cultivars of ber (Z. mauritiana) at Hisar (Bisla <strong>and</strong> Daulta, 1986). <strong>Ber</strong><br />
germplasm collection <strong>and</strong> evaluation at Amer, Bharatpur, Deeg, Tijara <strong>and</strong><br />
Jhunjhunu areas of Rajasthan, India indicated significant variation in<br />
physicochemical characteristics of 23 genotypes, <strong>and</strong> ten produced fruits of<br />
excellent quality (Lal et al., 2003). Variation in 10 local ber genotypes grown<br />
in West Bengal, were noted <strong>for</strong> soluble solids, total sugars, acidity <strong>and</strong> ascorbic<br />
acid content; ranges of <strong>the</strong>se parameters were 9.53-19.13 %, 4.94-12.30 %,<br />
0.38-2.60 % <strong>and</strong> 17.25-51.98 mg/100g respectively (Ghosh <strong>and</strong> Mitra, 2004).<br />
The cultivar Umran has 19 % TSS <strong>and</strong> 1.2 % acidity. In <strong>the</strong> case of Kathaphal,<br />
<strong>the</strong> TSS is 23 % <strong>and</strong> acidity was 0.77 % while in Gola, <strong>the</strong> TSS is 17-19 % <strong>and</strong><br />
0.46 - 0.5 % acidity. In Kaithali TSS is 18 % <strong>and</strong> acidity 0.5 % (Daulta <strong>and</strong><br />
Chauhan, 1982). Godara (1980) evaluated 16 cultivars <strong>for</strong> quality characters.<br />
The fruits of Mundia Murhara <strong>and</strong> Chhuhara had <strong>the</strong> highest TSS content (22.8<br />
<strong>and</strong> 22.4 %, respectively). Banarasi Karaka fruits had <strong>the</strong> highest nutritive<br />
value (Tiwari <strong>and</strong> Banafar, 1995). HB-1 <strong>and</strong> LB had excellent flavour <strong>and</strong> HB-<br />
2, KB1, SB <strong>and</strong> SB-2 were rated good at Bangalore. Under rainfed conditions<br />
of Bawal, Haryana cv. Nazuk had <strong>the</strong> highest total soluble solids (28.9 %)<br />
followed by Illaichi (Yamdagni et al., 1985 b).<br />
Kadaka had maximum sugar <strong>and</strong> minimum acidity content <strong>and</strong> was considered<br />
outst<strong>and</strong>ing (Singh <strong>and</strong> Singh, 1973). Some cultivars show variation in acidity<br />
(0.228-0.78 %) <strong>and</strong> ascorbic acid (80.85-178.04 mg/100 g pulp) (Godara,<br />
1980). Fruit ascorbic acid content of several cultivars ranged 70-165 mg/100g<br />
of pulp (Jaw<strong>and</strong>a <strong>and</strong> Bal, 1978). Bisla et al. (1980) observed <strong>the</strong> highest<br />
Vitamin-C content (120.15 mg/100g) in cv. Illaichi. The Vitamin-C content<br />
was highest in Narikelee, followed by Kaithali 165 <strong>and</strong> 125 mg/100g fruit pulp,<br />
respectively (Gupta, 1977). Jinsi 3 <strong>and</strong> Jinsi 4 (both small fruited), had sugar<br />
content over 35 % (Chen et al., 2003). Godhan was <strong>the</strong> most nutritive with<br />
regard to total soluble solids <strong>and</strong> ascorbic acid content, whereas Kharki was <strong>the</strong><br />
sweetest at Hoshangabad, Madhya Pradesh, India. The highest acidity (0.49 %)<br />
was exhibited by Soni while <strong>the</strong> lowest acidity (0.25 %) was exhibited by<br />
Kabra <strong>and</strong> Amrabati. The highest total sugar content (14.48 %) was exhibited<br />
100
y Bekanta <strong>and</strong> <strong>the</strong> lowest (8.5 %) by Karka (Gupta et al., 2004). The highest<br />
total soluble solids were recorded <strong>for</strong> Umran <strong>and</strong> <strong>the</strong> highest acid content in<br />
Sanaur 4 at Bhatinda (Tomar <strong>and</strong> Singh, 1987).<br />
Singh <strong>and</strong> Jindal (1980) found <strong>the</strong> highest contents of pulp (97.2 %) TSS (21.4<br />
%) <strong>and</strong> total sugar (10.7 %) in Gola Gurgaon, <strong>and</strong> Kaithli had <strong>the</strong> highest<br />
(113.5 mg/100 g) ascorbic acid content. The TSS content was highest in<br />
Chonchal <strong>and</strong> Illaichi <strong>and</strong> <strong>the</strong> latter cultivar had <strong>the</strong> highest ascorbic acid<br />
content. The highest content of non-reducing <strong>and</strong> total sugars was found in<br />
Chhuhara (Dhingra et al., 1973).<br />
Munier (1973) studied <strong>for</strong> quality characters. Cultivars grown in China, <strong>the</strong><br />
United States <strong>and</strong> Pakistan contained, respectively, 500-600, 300-500 <strong>and</strong> 45.2-<br />
160.8 mg Vitamin C/100 g. Variations in ascorbic acid content of 10 varieties<br />
have been reported by Ahmad <strong>and</strong> Malik (1971). Late ripening varieties<br />
generally contain more ascorbic acid than early ripening ones. Catechin content<br />
remains unchanged during <strong>the</strong> first half of <strong>the</strong> ripening period but declines 10-<br />
20 times below <strong>the</strong> original level during <strong>the</strong> later period. A close correlation<br />
was observed between ascorbic acid <strong>and</strong> catechin content during <strong>the</strong> ripening<br />
period (Kuliev <strong>and</strong> Akhundov, 1975).<br />
The most promising Ziziphus jujuba cultivars <strong>for</strong> quality were Nos. 1, 2 <strong>and</strong><br />
16/5. Ascorbic acid content was highest in Nikitskii 17 <strong>and</strong> Da-bai-tszao (774<br />
mg) <strong>and</strong> pectin content in U-sin-khun <strong>and</strong> Nikitskii 62 (up to 1 %) (Sin’ko,<br />
1974 b). He also listed <strong>the</strong> best varieties <strong>for</strong> conserving, drying <strong>and</strong> eating fresh<br />
among 25 cultivars studied <strong>for</strong> quality. Lomakina (1976) evaluated jujube<br />
varieties in south-west Turkmenistan. The best cultivars were Ya-tszao <strong>and</strong> Ta-<br />
Yan-tszao.<br />
The soluble protein in fruits <strong>and</strong> leaves on a fresh weight basis ranged from<br />
9.37 to 26.90 mg <strong>and</strong> 25.40 to 56.98 mg per gram respectively in 42 cultivars<br />
of Z. mauritiana (Sudhir et al., 1999). Umran was noted <strong>for</strong> high sugar <strong>and</strong><br />
protein contents, followed closely by Kathaphal (Khera <strong>and</strong> Singh, 1976). Free<br />
amino acids isolated from fruit pulp of wild taxa <strong>and</strong> 40 cultivars of Z.<br />
mauritiana did not show any relationship between <strong>the</strong> number <strong>and</strong> types of<br />
amino acids in wild samples <strong>and</strong> cultivars (Gill et al., 1997). In wild samples,<br />
<strong>the</strong> number of amino acids per sample was in <strong>the</strong> range 4-8. Of <strong>the</strong> 17 free<br />
amino acids represented in wild samples, glutamic acid, amino-butyric acid,<br />
threonine, proline <strong>and</strong> alanine were well represented. In cultivars <strong>the</strong> number of<br />
amino acids per sample was in <strong>the</strong> range 3-10. Of <strong>the</strong> 22 amino acids<br />
represented in <strong>the</strong>se cultivars, arginine, cysteine, cystine, alanine <strong>and</strong> proline<br />
were common. The most widely represented amino acids in cultivars (arginine,<br />
cysteine <strong>and</strong> cystine) were absent in wild taxa. The commonly represented<br />
amino acids in wild samples (glutamic acid, amino-butyric acid <strong>and</strong> threonine)<br />
were not common in cultivars. The free amino acid profile of fruit pulp was<br />
different from that of mature leaves in <strong>the</strong> same taxa.<br />
101
8.2.5 Genetic variability<br />
In<strong>for</strong>mation on genetic variability, heritability <strong>and</strong> correlation coefficients<br />
derived from data on leaf area, relative water content, stomatal index, stomatal<br />
frequency <strong>and</strong> yield in four year old ber plants of 12 popular ber cultivars,<br />
grown at Raichur, was observed. Genotypic coefficient of variation (GCV) <strong>and</strong><br />
phenotypic coefficient of variation (PCV) were greatest <strong>for</strong> stomatal frequency.<br />
GCV <strong>and</strong> PCV values were lowest <strong>for</strong> relative water content (RWC). High<br />
values of heritability <strong>and</strong> genetic gain were observed <strong>for</strong> stomatal index.<br />
Significant <strong>and</strong> positive correlations were observed between yield per plant <strong>and</strong><br />
stomatal frequency, leaf area <strong>and</strong> stomatal index (Praveen <strong>and</strong> Patil, 1998).<br />
High estimates of GCV, PCV, heritability <strong>and</strong> genetic advance were recorded<br />
<strong>for</strong> stone size, pulp stone ratio, fruit weight <strong>and</strong> yield indicating <strong>the</strong><br />
effectiveness of improvement through simple selection (Saran, 2005).<br />
8.2.5.1 Correlation <strong>and</strong> coefficients of variation<br />
The correlation coefficient of 12 growth, fruiting <strong>and</strong> quality characters of 24<br />
ber cultivars indicated that <strong>the</strong> stem girth was positively <strong>and</strong> significantly<br />
correlated with total soluble solids, leaf area with leaf dry weight, stone weight<br />
with acidity, fruit set with fruit drop, <strong>and</strong> negatively correlated with fruit set,<br />
<strong>and</strong> stone weight with fruit drop (Rajesh <strong>and</strong> Misra, 2004). Significant <strong>and</strong><br />
positive correlations were observed <strong>for</strong> leaf breadth, fruit diameter, fruit weight<br />
<strong>and</strong> fruit retention with yield. Selection of <strong>the</strong>se traits may be effective <strong>for</strong> <strong>the</strong><br />
improvement of ber (Gupta <strong>and</strong> Mehta, 2000). There were significant positive<br />
correlations between fruit yield, fruit set, <strong>and</strong> pulp/stone ratio of ber (cv.<br />
Umran) whereas yield had significant negative correlations with fruit drop <strong>and</strong><br />
stone weight. The total variation accounted <strong>for</strong> by all <strong>the</strong> characters was 86 %.<br />
Path analysis revealed a positive direct contribution of fruit set <strong>and</strong> fruit length<br />
<strong>and</strong> a negative contribution of fruit drop <strong>and</strong> stone weight. It is concluded that<br />
in breeding programmes importance should be given to <strong>the</strong>se four characters in<br />
developing high yielding ber genotypes (Prajapati et al., 1996).<br />
In a study of 30 cultivars at Hisar, India, fruit weight, fruit size, seed weight<br />
<strong>and</strong> pulp/stone ratio were significantly correlated with yield (Bisla <strong>and</strong> Daulta,<br />
1987). Yield was positively correlated with total sugar content <strong>and</strong> disease<br />
intensity (Bisla <strong>and</strong> Daulta, 1988b). Gola, Sanori No.5, Kishmish, Ponda <strong>and</strong><br />
Kaithali were found superior among <strong>the</strong> genotypes. TSS had positive <strong>and</strong> high<br />
correlation with total sugar while yield had negative correlation with quality<br />
traits except ascorbic acid <strong>and</strong> non-reducing sugars (Saran, 2005).<br />
The genetic co-efficient of variation measures <strong>the</strong> range of genetic variability<br />
which helps to compare <strong>the</strong> variability present in different genotypes. The<br />
genetic coefficient of variation ranged from three (fruit breadth) to 31.01%<br />
(yield kg/plant). Characters such as TSS, fruit breadth <strong>and</strong> fruit length showed<br />
comparatively low genetic coefficient of variation, whereas weight/fruit,<br />
102
pulp/stone ratio <strong>and</strong> yield (kg/plant) exhibited high genetic coefficient of<br />
variation.<br />
Correlation <strong>and</strong> path coefficients of eight commercial cultivars (Gola, Seb,<br />
Umran, Mundia, Illaichi, Tikkadi, Jogia <strong>and</strong> Bhagwadi) <strong>and</strong> three local<br />
selections of Z. rotundifolia were assessed <strong>for</strong> 13 yield attributes at Jobner,<br />
Rajasthan, India. Fruit set, fruit length, fruit breadth, fruit weight, stone<br />
diameter, pulp weight, specific gravity <strong>and</strong> harvest duration had significant<br />
positive correlation with fruit yield, whereas <strong>the</strong> fruit length had <strong>the</strong> highest<br />
direct positive effect on yield (Pareek et al., 2003).<br />
The success of any breeding programme depends on <strong>the</strong> extent of genetic<br />
variability in <strong>the</strong> source population. The assessment of variability is, <strong>the</strong>re<strong>for</strong>e,<br />
a basic requirement of breeding programmes. Since most of <strong>the</strong> plant characters<br />
of economic importance are governed by a group of genes <strong>and</strong> are highly<br />
influenced by environmental variation, it is difficult to judge whe<strong>the</strong>r <strong>the</strong><br />
observed variability is heritable or due to environment. This necessitates <strong>the</strong><br />
optimising of phenotypic variation into its heritable <strong>and</strong> non heritable<br />
components, <strong>and</strong> <strong>the</strong> more known about this, <strong>the</strong> better <strong>the</strong> characterisation of<br />
germplasm collections.<br />
The fruit weight, yield/plant <strong>and</strong> pulp/stone ratio in 13 Z. mauritiana cultivars<br />
showed high genetic coefficients of variation in Gujarat, India (Nanohar et al.,<br />
1986). Bisla <strong>and</strong> Daulta (1988a) also observed that <strong>the</strong> coefficient of variation<br />
was highest <strong>for</strong> fruit set (16.9) followed by <strong>the</strong> number of leaves per shoot<br />
(14.2), yield (12.9), fruit drop percentage, shoot length <strong>and</strong> tree height.<br />
Liu (1996) studied nine major quantitative characters of Chinese jujube. There<br />
was significant difference among characters in level of variation. The<br />
coefficient of variation was highest in fruit weight (51.95 %) <strong>and</strong> lowest in<br />
edible part of <strong>the</strong> fruit (2.67 %). Saran (2005) studied 10 quantitative characters<br />
<strong>for</strong> 35 genotypes. Saran (2005) also observed that high estimates of genetic<br />
coefficient of variation, phenotypic coefficient of variation, heritability <strong>and</strong><br />
genetic advance were recorded <strong>for</strong> stone size, pulp stone ratio, fruit weight <strong>and</strong><br />
yield. It indicates <strong>the</strong> effectiveness of improvement through selection. He<br />
observed that fruit yield had positive <strong>and</strong> significant correlation with tree<br />
spread (0.319) fruit weight (0.515) <strong>and</strong> stone size (0.353). He also observed<br />
that fruit size (0.580) <strong>and</strong> flesh thickness (0.811) were indirectly contributing<br />
via fruit weight. Fruit weight (0.998) contributed to yield mainly through its<br />
direct effect followed by <strong>the</strong> indirect effect of stone size <strong>and</strong> number of flowers<br />
per cyme.<br />
8.2.5.2 Path analysis<br />
Path analysis showed that fruit weight, seed weight <strong>and</strong> pulp/stone ratio had a<br />
positive, direct effect on yield of Z. mauritiana varieties (Bisla <strong>and</strong> Daulta,<br />
1987). Both total sugar content <strong>and</strong> disease intensity contributed directly to<br />
103
yield, <strong>and</strong> attention should be given to <strong>the</strong>se while selecting <strong>the</strong> genotypes <strong>for</strong><br />
improvement in yield (Bisla <strong>and</strong> Daulta, 1986).<br />
Correlation <strong>and</strong> path coefficients of 35 ber genotypes indicated that <strong>the</strong> traits<br />
like fruit weight, fruit size <strong>and</strong> stone size should be given due consideration<br />
while per<strong>for</strong>ming selection <strong>for</strong> yield in segregating generations of ber. So<br />
spread, fruit weight, stone size <strong>and</strong> fruit size were found to be effective<br />
selection indices. Yield of ber genotypes had significant positive correlation<br />
with spread, fruit weight <strong>and</strong> stone size. Fruit size had highly positive<br />
correlation with fruit weight <strong>and</strong> stone size. Fruit weight, fruit size <strong>and</strong> stone<br />
size were <strong>the</strong> main contributors towards yield which contribute via fruit weight<br />
(Saran, 2005).<br />
8.2.5.3 Inheritance<br />
Some work has been done to study <strong>the</strong> inheritance patterns of jujubes. Detailed<br />
genetic studies are yet to be carried out to unfold <strong>the</strong> riddles underlying<br />
heritability of quantitative <strong>and</strong> qualitative characters. Some attempts have been<br />
made in <strong>the</strong> past to underst<strong>and</strong> <strong>the</strong> genetic correlation between desirable traits.<br />
The inheritance of <strong>the</strong> characteristics chosen as breeding objectives will greatly<br />
influence <strong>the</strong> strategy employed <strong>for</strong> cultivar development. Qualitative<br />
characteristics controlled by one or a few major genes are more readily<br />
manipulated in a breeding programme than quantitative traits controlled by<br />
many genes (polygenes). Similarly characteristics whose expression is not<br />
influenced by <strong>the</strong> environment are more easily <strong>and</strong> effectively selected than<br />
those that are strongly affected by environmental factors.<br />
8.2.5.4 Heritability<br />
The estimation of heritability has been helpful to plant breeders, as it enables<br />
<strong>the</strong> selection programme to be based on phenotypic per<strong>for</strong>mance. Johnson et al.<br />
(1955) suggested that <strong>the</strong> heritability estimate in conjunction with genetic<br />
advance is usually helpful in predicting its resultant effect from selecting <strong>the</strong><br />
best individuals.<br />
Heritability in 30 ber cultivars ranged from 54.2 % <strong>for</strong> total soluble solids to<br />
99.63 % <strong>for</strong> disease intensity, <strong>and</strong> <strong>the</strong> value <strong>for</strong> acidity was 91.61 % (Bisla <strong>and</strong><br />
Daulta, 1988a). To improve <strong>the</strong> yield through hybridisation in Z. mauritiana<br />
individual trees with low fruit acidity <strong>and</strong> low disease intensity should be<br />
selected. Twelve cultivars evaluated <strong>for</strong> ten economic characters showed high<br />
heritability with high genetic advance <strong>for</strong> fruit weight <strong>and</strong> leaf length (Gupta<br />
<strong>and</strong> Mehta, 2000). Heritability was high <strong>for</strong> fruit weight (97.2 %) <strong>and</strong> size<br />
(87.9 %), pulp/stone ratio (87.5 %) <strong>and</strong> seed weight (84.6 %) in Z. mauritiana<br />
at Hisar (Bisla <strong>and</strong> Daulta, 1988b).<br />
The highest heritability values were seen <strong>for</strong> days from fruit set to ripening<br />
(99.2 %), fruit set (94.7 %), days from pruning to sprouting (93.6 %), fruit drop<br />
104
(85.0 %) <strong>and</strong> shoot length (82.0 %). High heritability coupled with genetic<br />
advance <strong>for</strong> yield (kg/plant), pulp/stone ratio indicated that high heritability<br />
obtained <strong>for</strong> <strong>the</strong>se characters was probably due to additive gene effect (Panse,<br />
1957). Expected genetic gain was highest <strong>for</strong> fruit set (142.8 %) <strong>and</strong> lowest <strong>for</strong><br />
days from pruning to flower initiation (3.5 %). Selection <strong>for</strong> higher fruit set <strong>and</strong><br />
lower fruit drop was recommended to improve <strong>the</strong> yield by Bisla <strong>and</strong> Daulta<br />
(1988a).<br />
Heritability estimates were moderate <strong>for</strong> fruit breadth (66.67) but low <strong>for</strong> fruit<br />
weight (44.03) in addition to fruit length. Heritability ranged from 42.25 %<br />
(fruit length) to 93.75 % (TSS). High heritability was expressed by yield<br />
(kg/plant) (91.62) <strong>and</strong> pulp/stone ratio (91.67) in addition to <strong>the</strong> TSS (Nanohar<br />
et al., 1986).<br />
High genetic advance has been reported in yield <strong>and</strong> pulp/stone ratio in<br />
different cultivars (Nanohar et al., 1986). Fruit weight, fruit size <strong>and</strong> seed<br />
weight showed high genetic advance (Bisla <strong>and</strong> Daulta, 1988b). The genetic<br />
advance expressed as percentage of mean ranged from 12.48% (fruit length) to<br />
61.16 % (yield/plant). The fruit length, fruit breadth <strong>and</strong> weight per fruit had<br />
low heritability along with low genetic advance, indicating that dominance of<br />
epistatic effect is of considerable value <strong>for</strong> <strong>the</strong>se characters <strong>and</strong> hence little<br />
improvement in <strong>the</strong>se characters is possible through selection. Individual plant<br />
selection <strong>for</strong> yield (kg/plant) <strong>and</strong> pulp/stone ratio would be satisfactorily<br />
effective in ber as <strong>the</strong>se characters exhibited high heritability as well as high<br />
genetic advance, whereas <strong>for</strong> <strong>o<strong>the</strong>r</strong> characters, selection may not be so<br />
effective.<br />
Saran (2005) studied 35 ber (Z. mauritiana) genotypes <strong>and</strong> revealed nine<br />
genetically divergent clusters (Table 8.1).<br />
105
Table 8.1 Classification of germplasm of ber in different clusters<br />
Clusters No. of Name of germplasm<br />
cultivars<br />
I 8 Kaithali, Govindgarh selection, Sanori No. 1,<br />
Noki, Chonchal, Mirchia, S<strong>and</strong>hura Narnul <strong>and</strong><br />
Jogia<br />
II 6 Seo, Laddu, Safeda Rohtak, D<strong>and</strong>an, Popular<br />
Gola <strong>and</strong> Seo Bhadurgarh<br />
III 1 Illaichi<br />
IV 5 Katha Rajasthan, Ponda, Gola, Sanori No. 5 <strong>and</strong><br />
Sua<br />
V 6 Katha Bombay, Bhadurgadhia, Thornless,<br />
Umran, Banarsi Karaka <strong>and</strong> Desi Alwar<br />
VI 2 Mundia Murhara <strong>and</strong> Bawal<br />
Selection-2<br />
VII 1 Chhuhara<br />
VIII 4 ZG-3, Akhrota, Gola Gurgaon No. 3 <strong>and</strong> Gola<br />
Gurgaon No. 2<br />
IX 2 Kathaphal <strong>and</strong> Kishmish<br />
8.2.6 Distribution of important traits<br />
The important traits in some ber cultivars have been described by Saran (2005)<br />
(Table 8.2) <strong>and</strong> <strong>the</strong> traits identified by <strong>o<strong>the</strong>r</strong>s are shown in Table 8.3.<br />
Table 8.2 Important traits in ber<br />
Cultivar<br />
Umran<br />
Ponda<br />
Sanori 5<br />
Laddu<br />
Gola<br />
Chhuhara<br />
Characters<br />
Yield, stem girth, fruit size, fruit weight, flesh thickness, flowers<br />
per cyme <strong>and</strong> pulp/stone ratio.<br />
Yield, spread, number of flowers per cyme, fruit weight, fruit size<br />
<strong>and</strong> flesh thickness.<br />
Yield, number of flowers per cyme, fruit weight, size of fruit <strong>and</strong><br />
flesh thickness.<br />
Yield, spread <strong>and</strong> number of flowers per cyme<br />
Spread, fruit weight, flesh thickness <strong>and</strong> stone weight<br />
Spread, stem girth<br />
Important traits have been identified by various workers which can be used by<br />
breeders; some breeders are listed in Table 8.4.<br />
106
Table 8.3 Traits identified in ber cultivars<br />
Traits Cultivars Author<br />
Fruit maturity Early (Gola, Mundia), mid season<br />
(Banarsi, Kaithli), late (Umran)<br />
Vashishtha,<br />
1983<br />
Sweetness (high<br />
TSS)<br />
Reshmi, Umran<br />
Vashishtha,<br />
1983<br />
Pulp texture Coconut-like (Umran), Juicy (Gola,<br />
Aliganj), Melting (Illaichi)<br />
Vashishtha,<br />
1983<br />
Fruit size<br />
Very large (Ponda), large (Umran),<br />
Medium (Mundia, Banarsi, Gola),<br />
small (Illaichi)<br />
Vashishtha,<br />
1983<br />
Fruit shape<br />
Fruit colour at<br />
maturity<br />
Acidity<br />
Shelf life of fruits<br />
Processing uses<br />
Apple like (Seb), cardamomshaped<br />
(Illaichi), bell shaped<br />
(Mundia), Round (Gola), oblong<br />
(Umran)<br />
Bright golden (Sanaur), bright<br />
yellow (Gola), Greenish yellow<br />
with brown blush (Kathaphal)<br />
Very low (Umran), low (Gola),<br />
Moderate acidic (Sanaur), acidic<br />
(Kathaphal)<br />
Good (Umran, Maharwali), poor<br />
(Gola)<br />
Dehydration (Vikas, Raja, Babu,<br />
Jeevan, Chinese cultivars, Umran,<br />
Bagwari, Chhuhara)<br />
Preserve (Umran, Banarsi Karaka,<br />
Kaithli)<br />
C<strong>and</strong>y (Illaichi, Umran, Kathaphal,<br />
Kaithli)<br />
Beverage (Gola, Mundia)<br />
107<br />
Vashishtha,<br />
1983<br />
Vashishtha,<br />
1983<br />
Vashishtha,<br />
1983<br />
Gopani, 1976 b<br />
Khurdiya, 1980<br />
Gupta et al.<br />
1981b<br />
Gupta et al.<br />
1981a<br />
Khurdiya <strong>and</strong><br />
Singh, 1975<br />
Resistance to fruitfly Tikadi, Meharun, Illaichi Singh <strong>and</strong><br />
Vashishtha,<br />
1984<br />
Resistance to fruit<br />
borer<br />
Tolerance to powdery<br />
mildew<br />
Banarsi Pew<strong>and</strong>i, Gola Gurgaon,<br />
Jhajjar Selection<br />
Illaichi Jhajjar, Sanaur-5, Safed<br />
Rohtak, Kathaphal, Gola, Seb,<br />
Meharun<br />
Dharkhi-1, Dharkhi-2, Guli,<br />
Field resistance to<br />
powdery mildew Villaiti, Seedless<br />
Tolerance to<br />
Isariopsis<br />
(Source: Pareek, 2001)<br />
Safed Rohtak, Sanaur-1, Seo<br />
Bahadugarhia, Jhajjar Selection,<br />
Pareek <strong>and</strong><br />
Vashishtha,<br />
1986<br />
Pareek <strong>and</strong><br />
Nath, 1996<br />
Pareek <strong>and</strong><br />
Nath, 1996<br />
Pareek <strong>and</strong><br />
Nath, 1996
8.3 Collections<br />
8.3.1 Genetic erosion<br />
Accelerated selection <strong>and</strong> wider adoption of clonally-propagated cultivars will<br />
lead to a degree of genetic erosion. However, whilst wild <strong>and</strong> naturalised<br />
populations persist in such large geographic areas in <strong>the</strong> primary centres of<br />
diversity, <strong>and</strong> numerous areas in <strong>o<strong>the</strong>r</strong> parts have become secondary centres,<br />
(e.g. tropical Africa <strong>for</strong> Z. mauritiana, Central Asia <strong>and</strong> South-west Asia <strong>and</strong><br />
parts of Africa <strong>for</strong> Z. jujuba), <strong>the</strong>re is not a major cause <strong>for</strong> concern.<br />
It is fairly common practice to top work wild trees with improved cultivars<br />
(Singh et al., 1973a; Yadav, 1991), <strong>and</strong> many rural communities use jujubes <strong>for</strong><br />
fencing, wind-breaks <strong>and</strong> <strong>o<strong>the</strong>r</strong> purposes. These activities provide a degree of<br />
protection.<br />
8.3.2 Existing collections<br />
Collections of germplasm which are currently maintained are largely geared to<br />
maintenance of cultivars <strong>and</strong> <strong>o<strong>the</strong>r</strong> selections, including in some cases mutants,<br />
which are used to support <strong>the</strong> national improvement ef<strong>for</strong>ts. Sometimes <strong>the</strong>y<br />
represent introductions which have been or might be tested <strong>for</strong> adaptation far<br />
from <strong>the</strong>ir places of origin. In effect, <strong>the</strong> collections are active collections ra<strong>the</strong>r<br />
than field gene-banks since costs of maintenance are related to utility ra<strong>the</strong>r<br />
than maintenance <strong>for</strong> long term conservation.<br />
As research progresses on characterisation <strong>and</strong> genetic affinities, it will be<br />
possible to develop strategic planning to rationalise existing collections so that<br />
synonyms of cultivars can be eliminated <strong>and</strong> <strong>the</strong> accessions can truly represent<br />
specific patterns of genetic variability <strong>and</strong> still be related to improvement<br />
needs, including ecological <strong>and</strong> climatic tolerances. Many of <strong>the</strong> traits<br />
considered in improvement are polygenic <strong>and</strong> <strong>the</strong>re will always be <strong>the</strong> need to<br />
err on <strong>the</strong> side of maintaining a larger number of accessions than actual<br />
utilisation needs require.<br />
A large number of Institutions particularly in India are holding ber germplasm<br />
<strong>and</strong> are working on <strong>the</strong>ir evaluation <strong>and</strong> improvement (Table 8.4).<br />
108
Table 8.4 Indian Institutions holding ber germplasm collections (number<br />
of accessions)<br />
Institutions<br />
Central Institute <strong>for</strong> Arid Horticulture,<br />
Bikaner - 334 006, Rajasthan, India<br />
Central Arid Zone Research Institute,<br />
Jodhpur -342 003, Rajasthan, India<br />
Indian Institute of Horticultural Research,<br />
Bangalore-560 089, Karnataka, India<br />
Central Horticultural Research Station,<br />
Godhra-389 001, Gujarat, India.<br />
Haryana Agricultural University,<br />
Hisar-125 004, Harayana, India<br />
Narendradeo University of Agriculture <strong>and</strong><br />
Technology, Kumarganj, Faizabad- 224<br />
229, U.P, India<br />
Mahatma Phule Agricultural University,<br />
Rahuri- 413 722, Maharasthra, India<br />
Gujarat Agricultural University,<br />
Sardar Krushinagar- 385 506, Gujarat,<br />
India<br />
Fruit Research Station, Punjab Agricultural<br />
University, Bahadurgarh, Patiala- 147 001,<br />
Punjab, India<br />
Indian Agricultural Research Institute,<br />
New Delhi - 110 012, India<br />
Dryl<strong>and</strong> Agriculture Research Station,<br />
Haryana Agricultural University, Bawal-<br />
123 501, Haryana, India<br />
(Pareek, 1988; Pareek <strong>and</strong> Sharma, 1993).<br />
Ziziphus <strong>Ber</strong> cultivars<br />
species<br />
7 162<br />
-- 68<br />
3 32<br />
-- 22<br />
-- 74<br />
-- 32<br />
-- 87<br />
-- 75<br />
-- 42<br />
4 52<br />
-- 36<br />
Chinese jujube is maintained at a number of sites in Hebei, Shanxi, Henan <strong>and</strong><br />
Shantung provinces <strong>and</strong> <strong>the</strong> Jujube Institute at <strong>the</strong> Hebei Agricultural<br />
University, Baodong, Hebei 071001 can always provide in<strong>for</strong>mation, as can <strong>the</strong><br />
Chinese Academy of Forestry.<br />
O<strong>the</strong>r collections of jujubes are to be found at <strong>the</strong> Apsheron Experimental<br />
Station <strong>for</strong> Subtropical <strong>Crops</strong>, Azerbaijan, where in <strong>the</strong> 1990s <strong>the</strong> best 40<br />
seedlings of ber were selected from 3762 jujube seedlings, <strong>and</strong> 25 were<br />
included among <strong>the</strong> elites. The 11 best <strong>for</strong>ms were given varietal names.<br />
A collection of subtropical fruits is maintained at <strong>the</strong> Turkmen Experimental<br />
Station Turkmenistan <strong>and</strong> includes several local, <strong>for</strong>eign <strong>and</strong> Soviet bred<br />
109
varieties of jujube. There are 65 <strong>for</strong>ms of Ziziphus jujuba at <strong>the</strong> Turkmen<br />
Experimental Station.<br />
A number of accessions of Z. jujuba are held at <strong>the</strong> Research Institute of Plant<br />
Production, Prague, Czechoslovakia. The Fruit-Tree Research Station (FTRS)<br />
in Japan has a collection of Z. jujuba maintained at <strong>the</strong> Okitsu Branch<br />
(Moriguchi et al., 1994).<br />
The National Germplasm System of <strong>the</strong> USA also holds significant accession<br />
numbers of <strong>the</strong> two major jujubes. European countries bordering <strong>the</strong><br />
Mediterranean have been involved in documenting germplasm of minor fruits,<br />
including jujubes, through a cooperative European Union Project, <strong>and</strong> national<br />
programmes recognised <strong>the</strong> need to collect materials in <strong>the</strong> latter part of <strong>the</strong><br />
1990s. Some work is still ongoing. Turkey also, through its national genetic<br />
resources programmes, maintains a number of accessions of Z. jujuba at<br />
ARARI, Meneme, Izmir.<br />
O<strong>the</strong>r countries maintain small collections of jujubes but <strong>the</strong>y are not<br />
maintained <strong>for</strong> genetic conservation but <strong>for</strong> short-term use e.g. Bangladesh<br />
maintains 35 accessions but only two of <strong>the</strong>se cultivars are under cultivation on<br />
farms (Saha, 1997). Similar collections are present in Korea, Pakistan <strong>and</strong><br />
Thail<strong>and</strong>.<br />
8.3.2.1 The need to consider rootstock resources<br />
In addition to cultivars more attention needs to be given to wild sources of<br />
current or potential use as rootstocks <strong>and</strong> <strong>the</strong>ir maintenance in <strong>the</strong> collections.<br />
Much of <strong>the</strong> research on using rootstocks, <strong>o<strong>the</strong>r</strong> than those of cultivars, has<br />
been hit <strong>and</strong> miss because very limited genetic material of each wild species<br />
used has been tested <strong>for</strong> rootstocks. Table 8.5 shows <strong>the</strong> situation <strong>for</strong> ber (Bal<br />
et al., 1997).<br />
Table 8.5 Species used <strong>for</strong> rootstocks <strong>for</strong> Indian jujube<br />
Compatibility<br />
Most successful<br />
Can be widely used<br />
Less successful but<br />
mostly compatible;often<br />
cultivar specific<br />
Species<br />
Z. mauritiana cultivars<br />
Z. mauritiana var. rotundifolia (wild/naturalised)<br />
Z. abyssinia<br />
Z. nummularia<br />
Z. xylopyrus<br />
Z. spina-christi<br />
Z. mucronata<br />
Z. oenoplia<br />
Z. jujuba<br />
Source: comprehensive summary by Pareek (2001).<br />
110
Chinese jujube rootstocks are most frequently wild materials (especially var.<br />
spinosa) related to <strong>the</strong> cultivars, but a number of <strong>o<strong>the</strong>r</strong> wild species have been<br />
tried in areas of China with more extreme climates (Ming <strong>and</strong> Sun, 1986).<br />
8.3.2.2 The need to consider wild species <strong>for</strong> breeding<br />
Wild species are sources of diversity <strong>for</strong> jujube improvement. Pareek (2001)<br />
noted <strong>the</strong> attributes of several in <strong>the</strong> case of ber (Table 8.6).<br />
Table 8.6 Exploitable attributes of wild species in ber improvement<br />
Wild Relatives<br />
Z. nummularia <strong>and</strong><br />
Z. lotus<br />
Exploitable Attributes<br />
i) Drought tolerance<br />
ii) Dwarf tree stature <strong>and</strong> extensive root system<br />
iii) Early fruit maturity<br />
Z. jujuba i) Resistance to low temperature damage<br />
ii) Excellent dehydration quality of fruits<br />
iii) High vitamin C <strong>and</strong> P contents in fruits<br />
Z. mistol i) Resistance to low temperature damage<br />
Z. mauritiana var.<br />
rotundifolia<br />
(Source: Pareek, 2001)<br />
8.3.4 Conservation methodologies<br />
i) Vigorous tree frame<br />
ii) Wood of marginal timber value<br />
Not a great deal of attention has been paid to storage of seeds of jujubes <strong>for</strong><br />
long-term conservation because of <strong>the</strong> heterozygosity present <strong>and</strong> <strong>the</strong> loss of a<br />
particular cultivar if seed is propagated.<br />
Two <strong>o<strong>the</strong>r</strong> factors are relevant. Firstly seeds of jujubes are not easy to h<strong>and</strong>le as<br />
seed ‘lots’, <strong>and</strong> secondly, regeneration of <strong>the</strong> sample when needed is difficult<br />
because it means growing out a tree population, waiting <strong>for</strong> fruiting age <strong>and</strong><br />
<strong>the</strong>n replacing a seed lot in cold storage.<br />
None<strong>the</strong>less, seeds of jujube species, both cultivated <strong>and</strong> wild show an<br />
orthodox behaviour when dried <strong>and</strong> stored at low temperatures. The<br />
Millennium Seed Bank of <strong>the</strong> Royal Botanic Gardens, Kew, UK stores<br />
accessions of Ziziphus, mostly wild species of arid zones of Africa. This<br />
institution has also looked at <strong>the</strong> relations between seed moisture contents,<br />
viability <strong>and</strong> storability at low temperatures. Fur<strong>the</strong>r in<strong>for</strong>mation is available at<br />
www.icuc-iwmi.org <strong>and</strong> advice can be given to any national programme<br />
considering placing jujube seeds into seed genebanks.<br />
The rationalisation of a number of <strong>the</strong> existing germplasm collections will<br />
enable <strong>the</strong>se to be transferred into field genebanks but <strong>the</strong>re are many gaps in<br />
<strong>the</strong> collections. Also more systematic evaluation of existing resources is<br />
essential to utilise <strong>the</strong> variable genepools. The lack of sufficient in<strong>for</strong>mation on<br />
111
per<strong>for</strong>mance accessions is due to <strong>the</strong> enormity of <strong>the</strong> task, <strong>and</strong> this has lead to<br />
<strong>the</strong>ir current limited use. Thus, proper characterisation <strong>and</strong> evaluation of<br />
germplasm <strong>and</strong> dissemination of <strong>the</strong> in<strong>for</strong>mation to breeders <strong>and</strong> <strong>o<strong>the</strong>r</strong>s is very<br />
important.<br />
8.3.4.1 The need <strong>for</strong> in situ conservation<br />
At present, much of <strong>the</strong> conservation is through use of <strong>the</strong> ranges of cultivars<br />
on-farm (e.g. Vietnam: see Le, 1998). Any on-farm conservation to be built<br />
into any national programme has to be based on farmers who are interested <strong>and</strong><br />
willing to do so. Natural genetic resources programmes are still grappling with<br />
principles, practices <strong>and</strong> policy issues in this area but those involved with<br />
jujube production should be part of <strong>the</strong> dialogues whenever possible.<br />
Many more practicable opportunities exist <strong>for</strong> conservation of Ziziphus in situ<br />
in natural habitats or in <strong>the</strong> areas where it grows naturally, achieved by<br />
protecting areas from human interference; such areas include natural parks,<br />
biosphere reserves or gene sanctuaries. A gene sanctuary is best located within<br />
<strong>the</strong> centre of origin of <strong>the</strong> crop species concerned, preferably covering <strong>the</strong><br />
micro-centre within <strong>the</strong> centre of origin (Singh, 2004). A gene sanctuary<br />
conserves <strong>the</strong> existing genetic diversity present in <strong>the</strong> population; it also allows<br />
<strong>for</strong> new gene combinations which appear with time. But it is difficult to<br />
establish <strong>and</strong> very difficult to maintain, especially in countries like India, which<br />
have an ever increasing population pressure. There is a need to establish gene<br />
sanctuaries in India <strong>for</strong> <strong>the</strong> conservation of Z. mauritiana <strong>and</strong> in China <strong>for</strong> Z<br />
jujuba. In situ conservation has two approaches i) biosphere reserve; (ii) habitat<br />
approach. The natural biosphere reserve is a useful solution <strong>for</strong> species that are<br />
endangered <strong>and</strong> almost on <strong>the</strong> point of extinction. Habitat approach refers to<br />
management of target species in its original habitat, through protected areas,<br />
managed <strong>for</strong>ests, natural reserves with multiple uses, preservation plots,<br />
wildlife sanctuaries, habitat or national parks <strong>and</strong> agro-ecosystems through onsite<br />
or on farm conservation.<br />
8.3.4.2 In vitro conservation<br />
In vitro genebanks can be very useful <strong>for</strong> clonally propagated material using<br />
slow growth in tissue culture <strong>and</strong> long-term cryopreservation of tissues <strong>and</strong>/or<br />
embryos. No such facilities exist <strong>for</strong> jujubes yet but a technique <strong>for</strong> in vitro<br />
storage of plants including Z. jujuba was developed in <strong>the</strong> Nikitsky Botanical<br />
Gardens, Ukraine (Mitrofanova et al., 2002). The growth of explants was<br />
retarded using physical (temperature, light <strong>and</strong> culture conditions), chemical<br />
(osmoticum application <strong>and</strong> optimization of culture medium) <strong>and</strong> plant<br />
physiological factors (plant age, dormancy <strong>and</strong> crop growth stage).<br />
112
Chapter 9. Harvesting, post-harvest<br />
h<strong>and</strong>ling <strong>and</strong> processing<br />
9.1 Introduction<br />
S. Azam-Ali<br />
This chapter is mainly devoted to ber. O<strong>the</strong>r jujube species show similarities in<br />
harvesting, ripening <strong>and</strong> grading requirements. After thorough discussion of<br />
ber, some details are added <strong>for</strong> Chinese jujube <strong>and</strong> Z. spina-christi.<br />
9.2 <strong>Ber</strong><br />
9.2.1 Harvesting<br />
<strong>Ber</strong> fruits should be harvested at <strong>the</strong> correct stage of maturity since <strong>the</strong>y do not<br />
mature after picking <strong>and</strong> <strong>the</strong> organoleptic (taste <strong>and</strong> texture) <strong>and</strong> visual<br />
qualities of fruits decline with increased maturity. Immature fruits lack<br />
sweetness <strong>and</strong> have an acrid taste. Over-mature or fully ripe fruits turn from<br />
yellow or golden-yellow colour to red or dark brown. The texture changes from<br />
crisp <strong>and</strong> juicy to soft <strong>and</strong> slimy. It is essential to harvest ber fruits at <strong>the</strong><br />
optimum stage of maturity. On <strong>the</strong> same tree, fruits ripen at different rates<br />
Fruits are ripe when <strong>the</strong>y are a golden yellow colour with a sweet <strong>and</strong> sour<br />
taste.<br />
9.2.1.1 Harvesting season<br />
The harvesting season varies according to cultivar <strong>and</strong> location. Some varieties<br />
ripen as early as October, <strong>o<strong>the</strong>r</strong>s ripen from mid-February until mid-March <strong>and</strong><br />
<strong>o<strong>the</strong>r</strong>s in March or mid-March until <strong>the</strong> end of April. In any location, diverse<br />
cultivars can be harvested over a period of months e.g. in North India from<br />
February to April, in west India from December to January, but in south India<br />
in November. In <strong>the</strong> Assiut Governorate <strong>the</strong>re are two crops a year, <strong>the</strong> main<br />
being in early spring <strong>and</strong> <strong>the</strong> second in <strong>the</strong> autumn (www.hort.purdue.edu). In<br />
India <strong>the</strong>re are two or three pickings which are done by h<strong>and</strong> ladders. One<br />
worker is capable of manually harvesting about 50 kg of fruit per day. After<br />
wrapping in white cloth, <strong>the</strong> fruits are put into paper-lined burlap bags of 50 kg<br />
capacity <strong>for</strong> carriage to markets throughout <strong>the</strong> country.<br />
9.2.1.2 Maturity st<strong>and</strong>ard<br />
Maturation time <strong>for</strong> ber fruits varies with genotype <strong>and</strong> environment. Some<br />
mature after 120 days while <strong>o<strong>the</strong>r</strong>s may take up to 170 days be<strong>for</strong>e <strong>the</strong>y are<br />
mature. Harvesting <strong>the</strong> fruits at <strong>the</strong> appropriate maturity is vital <strong>for</strong> improving<br />
<strong>the</strong> shelf-life <strong>and</strong> quality of <strong>the</strong> fruits. Maturity in ber fruits is usually judged by<br />
113
external colour. Fruits are harvested at <strong>the</strong> mature green <strong>and</strong> mature golden<br />
yellow stages depending on several factors: <strong>the</strong> cultivar, distance from market<br />
<strong>and</strong> expected post-harvest use.<br />
The various cultivars of ber mature at different rates <strong>and</strong> hence are harvested at<br />
different times. The Umran cultivar is best harvested at <strong>the</strong> mature golden<br />
yellow stage when fruits have good organoleptic qualities. They also have a<br />
low respiration rate <strong>and</strong> can be stored <strong>for</strong> long periods when harvested at this<br />
stage (Singh et al., 1981 a). Fruits of <strong>the</strong> cultivar Kaithli should be harvested at<br />
<strong>the</strong> green-yellow stage <strong>and</strong> <strong>the</strong> optimum stage <strong>for</strong> harvesting fruits of <strong>the</strong> Gola<br />
cultivar is <strong>the</strong> green mature, green-yellow or yellow stage (Siddiqui <strong>and</strong> Gupta,<br />
1989). Fully ripe fruits (red brown in colour) lose <strong>the</strong>ir crisp texture, but are<br />
suitable <strong>for</strong> dehydration.<br />
The total soluble solids (TSS) <strong>and</strong> <strong>the</strong> ratio of TSS to acid can be used as<br />
measures of fruit maturity. The TSS <strong>and</strong> TSS/acid ratio vary between cultivars.<br />
The optimum values are presented in Table 9.1. O<strong>the</strong>r indices such as <strong>the</strong><br />
degree day heat unit accumulation <strong>and</strong> fruit weight <strong>and</strong> volume have been<br />
suggested as viable indicators of maturity. However, <strong>the</strong>se measurements are<br />
ei<strong>the</strong>r less reliable than <strong>the</strong> visual colour method or not practical <strong>for</strong> use in <strong>the</strong><br />
field (Pareek, 2001).<br />
Table 9.1 Maturity indices <strong>for</strong> cultivars of ber (Bhatia <strong>and</strong> Gupta, 1985)<br />
Cultivar TSS (%) TSS/Acid ratio<br />
Gola 16.7-17.0 76-84<br />
Kaithli 16.2-16.5 75-100<br />
Umran 17.1-17.4 93-100<br />
The period <strong>for</strong> fruit development <strong>and</strong> maturation <strong>and</strong> subsequently <strong>the</strong> quality<br />
<strong>and</strong> shelf life of <strong>the</strong> fresh fruits also vary with cultivar. The cultivars are known<br />
to influence <strong>the</strong> quality of <strong>the</strong> fruits by <strong>the</strong>ir specific physico-chemical<br />
properties. For post-harvest use, <strong>the</strong> cultivar <strong>and</strong> its nutritional composition<br />
have to be considered as important traits that determine <strong>the</strong> most appropriate<br />
end use, <strong>the</strong> storage life <strong>and</strong> <strong>the</strong> quality of fruit. The cultivars Umran, Kathapal<br />
<strong>and</strong> Gola are <strong>the</strong> most promising varieties of ber in North India (Kudachikar et<br />
al., 2000).<br />
The different ber cultivars grown in north India have been studied <strong>for</strong> <strong>the</strong>ir<br />
physico-chemical attributes <strong>and</strong> have been grouped according to <strong>the</strong>ir physicochemical<br />
traits, harvesting season, suitability of specific cultivars <strong>for</strong> short <strong>and</strong><br />
long distance transport <strong>and</strong> <strong>the</strong> shelf life of harvested fruits.<br />
114
9.2.1.3 Attributes of important Indian ber fruits<br />
Umran<br />
This cultivar is commercially cultivated on a large scale in Punjab, <strong>and</strong><br />
Haryana states of India. It was developed from germplasm from Rajasthan at<br />
<strong>the</strong> Fruit Research Station at Bahadurgarch, Punjab. It fetches <strong>the</strong> highest<br />
price. The fruits are large sized, oval in shape <strong>and</strong> have a roundish apex. They<br />
weigh on average between 30 <strong>and</strong> 80 g. They are an attractive golden yellow<br />
colour which later turns into a chocolate brown at full maturity. The fruit<br />
matures in <strong>the</strong> mid-season (February to March) <strong>and</strong> ripens during mid-March to<br />
mid- April. The fruit is sweet with 19 % total soluble solids (TSS) <strong>and</strong> 0.12 %<br />
acidity. It has a pleasant flavour <strong>and</strong> excellent dessert quality. Umran fruits<br />
have a good keeping quality <strong>and</strong> can withst<strong>and</strong> long transportation. The main<br />
reason <strong>for</strong> its popularity is <strong>the</strong> long shelf life (15 to 20 days) <strong>and</strong> excellent<br />
organoleptic qualities. The fruit is also known locally as Ketha, Ajmeri <strong>and</strong><br />
Chamdi.<br />
Kathapal<br />
This is a late ripening cultivar of ber well known in Gujarat that has small to<br />
medium size fruits. At maturity, <strong>the</strong> fruits remain green on one side while <strong>the</strong><br />
<strong>o<strong>the</strong>r</strong> side develops a reddish yellow tinge. The average fruit weighs 10 g. They<br />
have a high TSS (23 %) <strong>and</strong> an acidity of about 0.77 %.<br />
Gola<br />
Gola is an early-maturing cultivar that is grown in Uttar Pradesh, Gujarat,<br />
Punjab, Rajasthan, Haryana <strong>and</strong> Delhi. It starts to bear fruit in <strong>the</strong> first week of<br />
January. The fruits are very attractive, roundish in shape <strong>and</strong> golden yellow in<br />
colour with an average weight of 20 g. The white flesh is very juicy, semi-soft<br />
<strong>and</strong> has a delicious taste. The fruit pulp has a TSS of 17 to 19 % <strong>and</strong> 0.46 to<br />
0.51 % acidity. The ratio of pulp to stone is 14.<br />
Kaithali<br />
This is a mid-season cultivar of ber well known in <strong>the</strong> Punjab that ripens during<br />
March. It was developed from <strong>the</strong> collection from <strong>the</strong> Kaithali area of<br />
Karukshestra in Haryana. The fruit is medium in size with an average weight of<br />
18 g, oval in shape <strong>and</strong> has a tapering apex. The fruit pulp is quite soft, has a<br />
TSS of 18 % <strong>and</strong> 0.5 % acidity. Unlike Umran, this fruit does not withst<strong>and</strong><br />
transportation <strong>and</strong> has a poor keeping quality.<br />
Tikadi.<br />
This ber cultivar is a late maturing type that ripens in Rajasthan during<br />
February <strong>and</strong> March. The fruits are small, weighing on average 10 g. The fruits<br />
become edible, with a creamy soft flesh, when <strong>the</strong> skin turns to a red colour<br />
during a short (7 to 10 day) ripening period of <strong>the</strong> fruits on <strong>the</strong> trees. The ripe<br />
fruit has a high TSS (25 %) with a large stone (<strong>the</strong> pulp to stone ratio of ripe<br />
fruit is 6.9).<br />
115
Jogia<br />
The fruits of this cultivar are also well known in Rajasthan <strong>and</strong> have a light<br />
purple tinge when <strong>the</strong>y are unripe, but are still edible at this time. Because of<br />
this, <strong>the</strong>y have an extended harvest period up to early February. The skin<br />
surface has coarse ridges <strong>and</strong> is greenish yellow in colour. The flesh is white,<br />
soft, juicy <strong>and</strong> sweet with a TSS of 19 % <strong>and</strong> a pulp to stone ratio of 14.<br />
Mundia<br />
This is an early Rajasthan, high yielding, cultivar that matures during mid-<br />
January. The fruits are large, juicy <strong>and</strong> bell shaped with an average weight of<br />
40 g. They have a yellowish green skin with smooth depressions. The flesh is<br />
white <strong>and</strong> soft with a TSS of 20 % <strong>and</strong> a pulp to stone ratio of 23.<br />
9.2.1.4 Harvesting method<br />
The most common method of harvesting ber fruits is by manually shaking or<br />
beating <strong>the</strong> tree branches to cause <strong>the</strong> ripe or mature fruits to fall to <strong>the</strong> ground.<br />
Sometimes a cloth is spread on <strong>the</strong> ground to facilitate collecting <strong>the</strong> fruits.<br />
Harvesting can also be carried out by mechanical shaking of <strong>the</strong> tree. Nei<strong>the</strong>r of<br />
<strong>the</strong>se methods of harvesting is very satisfactory as <strong>the</strong>y cause considerable<br />
damage to <strong>the</strong> fruit <strong>and</strong> <strong>the</strong> harvest includes a mixture of mature <strong>and</strong> immature<br />
fruit. <strong>Ber</strong> fruits ripen at different times even on a single tree <strong>and</strong> have a golden<br />
yellow appearance when <strong>the</strong>y are fully ripe. O<strong>the</strong>r more suitable methods of<br />
harvest include plucking <strong>the</strong> fruit using a clipper (an iron hook attached to a<br />
long bamboo pole) <strong>and</strong> h<strong>and</strong> picking <strong>the</strong> individual fruit. Both <strong>the</strong>se methods<br />
are more time consuming <strong>and</strong> more difficult <strong>and</strong> are <strong>the</strong>re<strong>for</strong>e not favoured by<br />
local farmers.<br />
In well managed fruit orchards, manual picking ensures <strong>the</strong> harvest of fruits<br />
with <strong>the</strong> pedicels 1 attached. Research has shown that fruits with <strong>the</strong> pedicel<br />
attached have a longer storage life (Pareek, 2001). Since ber fruits mature at<br />
different rates <strong>and</strong> do not ripen simultaneously, four to five or even up to seven<br />
pickings are needed to complete <strong>the</strong> harvest, especially <strong>for</strong> late maturing<br />
varieties such as Umran. This results in higher labour costs. The cumbersome<br />
picking operation <strong>and</strong> <strong>the</strong> associated costs could be markedly reduced by using<br />
suitable plant growth regulators. Indian researchers have investigated <strong>the</strong><br />
effects of applying plant growth regulators prior to harvest on <strong>the</strong> maturity <strong>and</strong><br />
subsequent ripening period of ber fruits. They have also looked at <strong>the</strong> ability of<br />
plant growth regulators to reduce spoilage during <strong>the</strong> pre-harvest <strong>and</strong> storage<br />
periods, <strong>and</strong> to improve <strong>the</strong> physico-chemical characteristics of <strong>the</strong> fruit.<br />
Ripening can be delayed <strong>and</strong> <strong>the</strong> number of pickings reduced by spraying with<br />
pre-harvest e<strong>the</strong>phon sprays (see Table 9.2). The application of <strong>the</strong> plant<br />
growth regulators can help to ensure early market returns or early <strong>and</strong> uni<strong>for</strong>m<br />
ripening of fruits.<br />
1 A small stalk, attached to <strong>the</strong> fruit<br />
116
Pre-harvest spraying of e<strong>the</strong>phon at 400 <strong>and</strong> 500 ppm to <strong>the</strong> Umran cultivar can<br />
accelerate <strong>the</strong> maturing of fruits. The mature fruits turn a deep golden yellow<br />
colour <strong>and</strong> have a high total soluble solids content, ascorbic acid <strong>and</strong> total<br />
sugars <strong>and</strong> a low specific gravity <strong>and</strong> acidity. Fur<strong>the</strong>r, <strong>the</strong>se treated fruits<br />
become more palatable <strong>and</strong> can be ripened two weeks earlier than untreated<br />
ones. The benefit of inducing maturity is that early ripened fruits could fetch a<br />
higher market price. Also, <strong>the</strong> harvesting period can be stretched from two to<br />
four weeks which would ease <strong>the</strong> strain of marketing at peak ripening time.<br />
Table 9.2 The effects of spraying E<strong>the</strong>phon on <strong>the</strong> number of harvests of<br />
ber fruit (Pareek <strong>and</strong> Nath, 1996)<br />
E<strong>the</strong>phon (ppm)<br />
Cultivar<br />
Gola<br />
Sev<br />
0 5 4<br />
500 4 3<br />
750 3 2<br />
1000 3 3<br />
9.2.1.5 Fruit growth <strong>and</strong> maturation<br />
<strong>Ber</strong> requires a relatively long period of 150 to 190 days (22 to 27 weeks) after<br />
fruit set <strong>for</strong> fruit growth <strong>and</strong> maturation. Some cultivars grown in <strong>the</strong> Hissar<br />
region of <strong>the</strong> north of India can be harvested at 120 days after fruit set. The<br />
fruit growth period can be divided into three distinct phases:<br />
1. <strong>the</strong> most active fruit growth phase during <strong>the</strong> first 6 to 7 weeks<br />
2. slow growth rate <strong>for</strong> <strong>the</strong> middle eight weeks<br />
3. active growth rate <strong>for</strong> <strong>the</strong> last 8 to 10 weeks.<br />
Studies on <strong>the</strong> developmental physiology of fruit of <strong>the</strong> Umran cultivar in <strong>the</strong><br />
Punjab illustrate <strong>the</strong> distinct physical <strong>and</strong> chemical changes during <strong>the</strong> growth<br />
<strong>and</strong> development of <strong>the</strong> fruit. Fruits of cultivar Umran attain <strong>the</strong> ripe stage in<br />
190 days after fruit set. Fruit growth in terms of length <strong>and</strong> diameter showed<br />
three distinct phases. The increase in length was faster than <strong>the</strong> growth of <strong>the</strong><br />
diameter during <strong>the</strong> first phase. Conversely, during <strong>the</strong> third phase, <strong>the</strong> increase<br />
in diameter was greater than <strong>the</strong> increase in length. That is, <strong>the</strong> fruits grew in<br />
length at <strong>the</strong> start of <strong>the</strong>ir growing period <strong>and</strong> ‘filled out’ during <strong>the</strong> final<br />
growth phase.<br />
The major chemical changes that take place during fruit growth <strong>and</strong><br />
development are changes in <strong>the</strong> content of total soluble solids (TSS). The TSS<br />
increases from fruit set through to ripening. This increase is very pronounced<br />
during <strong>the</strong> latter stages of maturity. There is a corresponding decrease in<br />
acidity (an increase in pH) of <strong>the</strong> fruit pulp as <strong>the</strong> fruit ripens. When <strong>the</strong> fruit is<br />
physiologically mature, <strong>the</strong> fruit colour turns to dark green followed by<br />
ripening with a change in colour as <strong>the</strong> ripening process advances. The stalk<br />
end of <strong>the</strong> fruit starts to turn yellow <strong>and</strong> later turns to bright yellow <strong>and</strong> <strong>the</strong>n<br />
117
own at <strong>the</strong> end of ripening. There is a wide variation in <strong>the</strong> TSS (12.2 to<br />
19.2° Brix) <strong>and</strong> acidity (0.23 to 0.52 %) in different cultivars of <strong>the</strong> ripe fruit<br />
(Teaotia et al., 1974). Changes in <strong>the</strong> levels of <strong>o<strong>the</strong>r</strong> chemical components such<br />
as ascorbic acid, total phenolics <strong>and</strong> minerals during <strong>the</strong> maturation of ber<br />
fruits have been reported (Bal <strong>and</strong> Singh, 1987). The level of ascorbic acid<br />
gradually increased during growth <strong>and</strong> development (from 15 days after fruit<br />
set until 190 days). The total phenolics content increased initially, reached a<br />
peak in <strong>the</strong> developing fruits <strong>and</strong> later showed a fall as fruit maturity advanced.<br />
The calcium content showed a gradual downward trend up to 150 days <strong>and</strong><br />
<strong>the</strong>n remained constant until ripening. The phosphorus content showed a steady<br />
decline with <strong>the</strong> advancement of maturity. The iron content remained almost<br />
constant in <strong>the</strong> beginning <strong>and</strong> <strong>the</strong>reafter gradually decreased towards ripening.<br />
9.2.1.6 Fruit drop <strong>and</strong> its control<br />
Fruit drop is a major <strong>and</strong> serious problem in ber production. Generally <strong>the</strong><br />
number of fruit set is very high, but <strong>the</strong> extent of fruit retention varies<br />
according to <strong>the</strong> cultivar type <strong>and</strong> on <strong>the</strong> level of production of endogenous<br />
plant hormones. Several studies have been made on fruit set, fruit drop <strong>and</strong><br />
level of fruit retention. Sharma et al., (1990) found that early maturing cultivars<br />
(that were eight years of age) were resistant to fruit drop while <strong>the</strong> late cultivars<br />
were <strong>the</strong> most susceptible to fruit drop. Garwal et al. (1993) observed a similar<br />
pattern, but also noticed that <strong>the</strong> fruit drop in later maturing cultivars (var.<br />
Sendbura <strong>and</strong> Narnaul) could be controlled by spraying <strong>the</strong> fruit with 10 ppm<br />
of NOXA growth regulator. This treatment resulted in <strong>the</strong> production of large<br />
size fruits with significantly higher total soluble solids <strong>and</strong> ascorbic acid<br />
content <strong>and</strong> lower acidity, total sugars <strong>and</strong> reducing sugar content than most<br />
<strong>o<strong>the</strong>r</strong> treatments.<br />
9.2.1.7 Time of harvest <strong>and</strong> fruit yield<br />
The time of harvest affects <strong>the</strong> storage life of fruits. For practical reasons,<br />
harvesting in <strong>the</strong> morning is generally preferred as <strong>the</strong> fruits are cool <strong>and</strong> turgid<br />
at this time of day <strong>and</strong> can be sold or fur<strong>the</strong>r processed <strong>the</strong> same day. However,<br />
one study reported that fruits harvested at midday had a better storage life than<br />
those harvested in <strong>the</strong> morning or evening. This may be due to greater loss of<br />
water from <strong>the</strong> morning or evening harvested fruits (Pareek, 2001).<br />
Bal et al. (1995) reported that <strong>the</strong> pre-harvest spray of e<strong>the</strong>phon at a<br />
concentration of 300 ppm to ber trees induced uni<strong>for</strong>m ripening of fruits, <strong>and</strong><br />
<strong>the</strong> fruits harvested at optimum maturity could be stored <strong>for</strong> up to <strong>for</strong>ty days at<br />
a temperature of 0 to 3.3° C <strong>and</strong> relative humidity of 85 to 90 %.<br />
<strong>Ber</strong> trees can produce fruit after <strong>the</strong> first year of planting from budded plants or<br />
after in situ budding in <strong>the</strong> field. However, during <strong>the</strong> first two years in <strong>the</strong><br />
tropics, <strong>and</strong> three years in <strong>the</strong> sub-tropics, young plants are trained to develop<br />
into well balanced trees ra<strong>the</strong>r than <strong>for</strong> fruit production. Fruit production<br />
<strong>the</strong>re<strong>for</strong>e starts from <strong>the</strong> third year in <strong>the</strong> tropics <strong>and</strong> <strong>the</strong> fourth year in <strong>the</strong> sub-<br />
118
tropics. <strong>Ber</strong> trees can become prime fruit bearers at an early age (i.e. from <strong>the</strong><br />
fifth to sixth year under intensive management).<br />
The fruit yield per tree varies with cultivar, age of <strong>the</strong> tree, climate <strong>and</strong> location<br />
of <strong>the</strong> tree. Seedling trees bear between 5000–10,000 fruits per year <strong>and</strong><br />
superior grafted trees can bear up to 30,000 fruits. The best cultivar in India<br />
reportedly bears fruits that give an average of 66 fruits per kg <strong>and</strong> that yields 77<br />
kg annually. Both fruit size <strong>and</strong> number can be increased by simple cultural<br />
treatment (www.hort.purdue.edu). Yields of 80 to 200 kg per mature (10 to 20<br />
year old) tree have been reported in India <strong>for</strong> trees under irrigated conditions.<br />
Yields as low as 50-75 kg per tree have also been reported. In Israel, yields of<br />
12 tons per hectare have been obtained from three year old ber trees (Pareek,<br />
2001). Water availability has a significant impact on yield. In rainfed<br />
agriculture, <strong>the</strong> yield can be as low as 80-100 kg per tree in semi-arid areas,<br />
while in arid areas it can fall to 50 kg per tree (see Pareek, 2001).<br />
Researchers in India (Kudachikar et al., 2000) have investigated <strong>the</strong> effect of<br />
pruning <strong>the</strong> tree on fruit yield <strong>and</strong> quality. Pruning is considered to be one of<br />
<strong>the</strong> most important horticultural practices <strong>for</strong> <strong>the</strong> production <strong>and</strong> maintenance<br />
of regular fruit bearing, both in terms of quality <strong>and</strong> quantity of fruit. <strong>Ber</strong> fruits<br />
are borne in <strong>the</strong> leaf axils on <strong>the</strong> young growing shoots of <strong>the</strong> current season.<br />
Pruning has been discussed in Chapter 6 but details relevant <strong>for</strong> fruiting are<br />
provided below. The best time <strong>for</strong> pruning ber trees is during <strong>the</strong> hot <strong>and</strong> dry<br />
season when <strong>the</strong> tree sheds its leaves <strong>and</strong> becomes dormant after <strong>the</strong> harvesting<br />
of fruits (Sharma <strong>and</strong> Kore, 1990). The effects of severity of pruning on<br />
flowering, fruit setting, fruit yield <strong>and</strong> quality of ber fruits of different cultivars<br />
in different agro-climatic growing regions have been investigated by Bajwa et<br />
al, (1986), Bisla et al. (1991) <strong>and</strong> Kundu et al, (1994).<br />
Kundu et al. (1994) looked at pruning of thirteen year old Umran trees. When<br />
pruning was too severe <strong>and</strong> <strong>the</strong> planting distance close, flowering <strong>and</strong> fruit<br />
production was decreased. However, when <strong>the</strong> planting distance was wider,<br />
even though <strong>the</strong> pruning was severe, <strong>the</strong> percentage of fruit set increased. The<br />
percentage of fruit retention increased with increased planting distance <strong>and</strong><br />
decreased pruning severity. Yadhav <strong>and</strong> Godara (1992) found that <strong>the</strong> best<br />
combination <strong>for</strong> ber trees was medium pruning combined with a planting<br />
distance of 7.2 m x 7.2 m or 9.6 m x 9.6 m.<br />
The fruit yield in un-pruned trees is often on a par with pruned trees, but <strong>the</strong><br />
fruit quality is poor. Pruned trees tend to produce large fruits of good quality<br />
<strong>and</strong> with a significantly higher fruit weight.<br />
As noted in 9.2.1.4 researchers have investigated <strong>the</strong> effects of applying plant<br />
growth regulators prior to harvesting on fruit maturity, yield <strong>and</strong> quality. The<br />
application of calcium compounds such as calcium chloride <strong>and</strong> calcium nitrate<br />
(CCC) at 1.7 g per litre as a pre-harvest spray reduced <strong>the</strong> fruit weight loss,<br />
119
delayed colour development <strong>and</strong> maintained good quality ber fruits during<br />
storage (Gupta et al., 1987). Bankar <strong>and</strong> Prasad (1990) investigated <strong>the</strong> effects<br />
of pre-harvest spraying of ber fruit with gibberellic acid (GA3) <strong>and</strong> napthalein<br />
acetic acid (NAA) at three different rates (10, 20 <strong>and</strong> 30 ppm) ei<strong>the</strong>r alone or in<br />
combination at two different times (at <strong>the</strong> time of flowering <strong>and</strong> at 15 days after<br />
flowering). They found that both growth regulators, at all concentrations <strong>and</strong><br />
applied at both times, alone <strong>and</strong> in combination, increased <strong>the</strong> number of fruit<br />
set <strong>and</strong> decreased fruit drop (i.e. <strong>the</strong>y increased fruit retention). The fruit<br />
weight <strong>and</strong> fruit length were both significantly increased by application of GA3<br />
or NAA at 30 ppm concentration. The total soluble solids (TSS) content was<br />
improved by treatment with GA3. Masalkar <strong>and</strong> Wavhal (1991) reported that<br />
<strong>the</strong> pre-harvest application of GA3 (10-20 ppm) <strong>and</strong> e<strong>the</strong>phon (400 ppm) to ber<br />
trees of Umran cultivar improved <strong>the</strong> physico-chemical characteristics of ber<br />
fruits. Significant increase in fruit weight, fruit volume, pulp percentage, nonreducing<br />
sugars <strong>and</strong> ascorbic acid contents <strong>and</strong> lower stone percentage were<br />
obtained with treatments of GA3 alone, while e<strong>the</strong>phon treatment resulted in<br />
high TSS content <strong>and</strong> also improved <strong>the</strong> fruit colour to golden yellow. O<strong>the</strong>r<br />
growth regulators have been tested; 2,4-D at 10-15 ppm <strong>and</strong> CCC at 100 ppm<br />
but CCC can reduce <strong>the</strong> size of fruits.<br />
9.2.2 Post harvest h<strong>and</strong>ling<br />
9.2.2.1 Post harvest ripening<br />
After harvest at <strong>the</strong> mature green to mature golden yellow stages, ber fruits<br />
start to ripen at ambient temperature. Ripening is signified by a change in<br />
colour from green or golden yellow to red or red brown. It takes place after 4 to<br />
15 days, depending upon cultivar <strong>and</strong> storage environment.<br />
The fruits are considered to have <strong>the</strong> best organoleptic qualities (taste <strong>and</strong><br />
texture) when <strong>the</strong>y are at <strong>the</strong> mature green to mature golden yellow stages.<br />
There<strong>for</strong>e, attempts are made to delay <strong>the</strong> ripening process <strong>and</strong> prolong <strong>the</strong><br />
keeping quality by modifying <strong>the</strong> storage environment.<br />
Plant growth regulators may be applied to ber fruits after harvest to accelerate<br />
<strong>the</strong> uni<strong>for</strong>m rate of ripening <strong>and</strong> to reduce losses through post-harvest decay.<br />
E<strong>the</strong>phon has been found to be <strong>the</strong> most effective growth regulator that<br />
accelerates <strong>the</strong> ripening <strong>and</strong> improves <strong>the</strong> quality of ber fruit (Kudachikar et al.,<br />
2000). Siddiqui <strong>and</strong> Gupta (1995) found that post harvest dipping of ber fruits<br />
(cultivar Umran) at <strong>the</strong> colour turning stage in cycocel or chloromequot (500 or<br />
1000 ppm) <strong>for</strong> 15 minutes, followed by storage in wooden boxes packed with<br />
newspaper at 25 ± 5° C significantly reduced <strong>the</strong> decay loss of fruits <strong>and</strong><br />
retarded <strong>the</strong> ripening process, <strong>the</strong>reby extending <strong>the</strong> shelf-life of fruits.<br />
9.2.2.2 Grading<br />
The harvested fruits are usually at different stages of maturity <strong>and</strong> need to be<br />
sorted into different groups be<strong>for</strong>e <strong>the</strong>y are sold, stored or fur<strong>the</strong>r processed.<br />
120
They are sorted <strong>and</strong> graded according to maturity, size, shape <strong>and</strong> colour. First<br />
<strong>the</strong> fruits are sorted by h<strong>and</strong>. The under-ripe, over-ripe, damaged <strong>and</strong><br />
misshapen fruits are removed. The under-ripe fruits are set aside <strong>and</strong> left to<br />
ripen. Over-ripe fruits are not desirable <strong>for</strong> fresh sales or processing <strong>and</strong> should<br />
be discarded.<br />
The remaining fruits are graded into two or three groups based on <strong>the</strong> size <strong>and</strong><br />
colour of fruit. Grading can ei<strong>the</strong>r be carried out manually or by passing<br />
through sieves of different mesh sizes. A grading st<strong>and</strong>ard <strong>for</strong> ber fruits is<br />
included in Table 9.3.<br />
Table 9.3 Grading criteria <strong>for</strong> ber (Pareek <strong>and</strong> Gupta, 1988)<br />
Grade St<strong>and</strong>ard<br />
A Shining yellow, large (>35 mm) to medium size (24-35 mm)<br />
fruits of uni<strong>for</strong>m size with no blemishes.<br />
B Uneven yellow or yellow red, large (>35 mm) to medium (25-35<br />
mm) fruits of uni<strong>for</strong>m shape with some blemishes.<br />
C Red, large (>35 mm) to small (
leach powder per kg of fruit. Diphenyl impregnated paper can also be used <strong>for</strong><br />
packaging to reduce bacterial spoilage (Pareek, 2001).<br />
The use of chemical preservatives is not always desirable. It is preferable to<br />
pack ber fruits in non-organic materials, which avoids <strong>the</strong> need <strong>for</strong> chemicals.<br />
Per<strong>for</strong>ated poly<strong>the</strong>ne bags (150 gauge), nylon nets or cardboard cartons can be<br />
used to package small quantities of 1-2 kg. For larger volumes of fruit of 10-<br />
20kg, gunny bags, cloth packages or wooden boxes with holes or slits are used.<br />
Baskets made from locally available materials such as bamboo can be used.<br />
Shredded paper is <strong>the</strong> best material to use <strong>for</strong> cushioning <strong>and</strong> protection during<br />
transport.<br />
For transportation, corrugated cardboard cartons of about 10 kg are <strong>the</strong> most<br />
suitable packaging material. For short distances, cheaper materials such as<br />
gunny bags, cloth or old boxes can be used provided that <strong>the</strong> fruit are<br />
cushioned <strong>and</strong> ventilation is provided. The best packages are nylon nets or<br />
per<strong>for</strong>ated poly<strong>the</strong>ne bags <strong>for</strong> small quantities of about 1 to 3 kg fruit <strong>for</strong> retail<br />
sale.<br />
9.2.2.4 Storage<br />
<strong>Ber</strong> fruits are relatively perishable <strong>and</strong> have a shelf life of only four to five days<br />
at ambient temperatures. Transportation of ripe fruits to distant places is<br />
difficult <strong>and</strong> results in large post-harvest losses. Both pre-harvest <strong>and</strong> postharvest<br />
factors have been found to influence <strong>the</strong> storage life <strong>and</strong> post-harvest<br />
quality of ber fruits (Kudachikar et al., 2000). Pre-harvest factors that influence<br />
<strong>the</strong> storage life include <strong>the</strong> following:<br />
pruning of <strong>the</strong> tree<br />
control of fruit drop by exogenous application of plant growth<br />
regulators<br />
<strong>the</strong> stage of maturity<br />
physico-chemical composition of <strong>the</strong> fruits at <strong>the</strong> time of harvest.<br />
Post-harvest factors that influence storage life <strong>and</strong> fruit quality include <strong>the</strong><br />
following:<br />
<strong>the</strong> use of plant growth regulators<br />
irradiation<br />
storage conditions<br />
Storage experiments in India have demonstrated that slightly under-ripe fruits<br />
ripen <strong>and</strong> keep <strong>for</strong> eight days under wheat straw, seven days under leaves <strong>and</strong><br />
four days in carbide (50 to 60 g) (www.hort.purdue.edu). O<strong>the</strong>r studies in India<br />
(Kudachikar et al., 2000), demonstrated that <strong>the</strong> shelf life of ber fruits could be<br />
significantly extended by coating <strong>the</strong> fruits in wax, packing <strong>the</strong>m in<br />
polyethylene bags <strong>and</strong> storing at 0 to 3.3° C <strong>and</strong> 0 to 4° C, up to 40 days <strong>and</strong> 21<br />
days respectively. This is in comparison to untreated fruits that are stored at<br />
ambient temperature (30 to 35° C) <strong>and</strong> only have a maximum shelf life of<br />
122
seven days. The improved storage life at reduced temperatures gives potential<br />
<strong>for</strong> transporting ber over long distances, from <strong>the</strong> growing areas in North India<br />
to consumers in sou<strong>the</strong>rn India, if refrigerated transport lorries are available.<br />
Storage at room temperature<br />
After harvest, ber fruits are usually stored at ambient temperature (25-35° C)<br />
until <strong>the</strong>y are ei<strong>the</strong>r sold or fur<strong>the</strong>r processed. The fruit is often stored in heaps<br />
under shade or in storage rooms, but it is better to store in packages such as<br />
gunny bags, net bags, poly<strong>the</strong>ne bags <strong>and</strong> boxes. Depending upon cultivar <strong>and</strong><br />
<strong>the</strong> storage conditions, fruit can be kept <strong>for</strong> 4 to 15 days without loss of<br />
organoleptic quality.<br />
During storage, <strong>the</strong> fruits lose weight <strong>and</strong> shrivel, change colour from green<br />
yellow or golden yellow to reddish brown <strong>and</strong> lose acidity <strong>and</strong> ascorbic acid<br />
(vitamin C), but gain in sweetness. Typical values <strong>for</strong> quality parameters of ber<br />
fruits (cultivar Umran) in storage are found in Table 9.4.<br />
Table 9.4. Typical changes in quality characteristics of ber fruit during<br />
storage at ambient temperature (from Pareek, 2001)<br />
<strong>Ber</strong> fruits (Umran cultivar)<br />
Quality parameters At harvest After 9 days storage<br />
at 30-35°C<br />
Colour Golden yellow Grey orange<br />
TSS (%) 17.5 19.5<br />
Total sugars (%) 10.19 16.38<br />
Acidity (%) 0.21 0.12<br />
Ascorbic acid<br />
117.13 93.72<br />
(mg/100g)<br />
Total phenolics (%) 0.108 0.039<br />
Cool storage<br />
The shelf life of fruits can be extended by storage in cool chambers. Cool<br />
chambers are simple, double walled structures made from locally available<br />
materials such as mud or brick. The space between <strong>the</strong> two walls is filled with<br />
s<strong>and</strong> or wood shavings that are kept cool by sprinkling with water. Cooling is<br />
achieved by evaporation of water from <strong>the</strong> walls of <strong>the</strong> chamber.<br />
With prolonged storage in a cool chamber, a high level of humidity can<br />
develop within <strong>the</strong> chamber which is conducive to spoilage in <strong>the</strong> fruit. Fruits<br />
have been stored successfully <strong>for</strong> 6 to 10 days in cool chambers without any<br />
loss in quality. However, <strong>the</strong> length of storage within a cool chamber very<br />
much depends on <strong>the</strong> cultivar, ambient <strong>and</strong> internal temperature, humidity<br />
level, quantity of fruit within <strong>the</strong> chamber <strong>and</strong> <strong>the</strong> maturity of <strong>the</strong> fruit at<br />
harvest.<br />
123
If cold storage is available, fruits can withst<strong>and</strong> temperatures as low as 10° C<br />
without any damage. At this temperature, <strong>the</strong> shelf life can be extended <strong>for</strong> 28<br />
to 42 days depending upon cultivar. At temperatures of 13° C, fruits can be<br />
stored in per<strong>for</strong>ated poly<strong>the</strong>ne bags <strong>and</strong> baskets <strong>for</strong> up to 3 weeks without any<br />
loss in quality (Pareek, 2001). At lower storage temperatures (at 0 to 4° C), <strong>the</strong><br />
fruits become an unattractive brown colour.<br />
Treatments to extend shelf life<br />
Various treatments are available to extend <strong>the</strong> shelf life of fruits. Some of <strong>the</strong>se<br />
are applied to <strong>the</strong> fruit whilst still on <strong>the</strong> tree while <strong>o<strong>the</strong>r</strong>s are post-harvest<br />
treatments. The use of <strong>the</strong> various chemicals to extend <strong>the</strong> storage life of fruits<br />
should be carried out with caution, especially if <strong>the</strong> fruit is being sold as<br />
organic. Certain chemicals are not permissible <strong>for</strong> use on fruits that are<br />
destined <strong>for</strong> <strong>the</strong> organic market. National <strong>and</strong> international regulations should<br />
be consulted regarding <strong>the</strong> use of any chemical. All safety regulations<br />
regarding <strong>the</strong> dosage <strong>and</strong> application of spray <strong>and</strong> <strong>the</strong> use of <strong>the</strong> fruit after<br />
spraying, <strong>for</strong> example, <strong>the</strong> number of days that must elapse be<strong>for</strong>e <strong>the</strong> fruit is<br />
safe <strong>for</strong> consumption, should be observed.<br />
Pre-harvest treatments<br />
The calcium content of fruits influences <strong>the</strong> shelf life. There<strong>for</strong>e, pre-harvest<br />
applications of calcium compounds can have an effect on <strong>the</strong> storage life.<br />
Fruits naturally contain calcium as compounds of pectate, carbonate, oxalate<br />
<strong>and</strong> phosphate. One treatment is to spray <strong>the</strong> fruit 10 days be<strong>for</strong>e harvest with a<br />
solution of calcium chloride at 1.7 g calcium per litre with 1 % Teepol as a<br />
surfactant. A second treatment is to apply calcium nitrate to <strong>the</strong> fruit. A 1 %<br />
solution of calcium nitrate is sprayed on <strong>the</strong> fruit 10 days be<strong>for</strong>e harvest, when<br />
<strong>the</strong> fruit is at <strong>the</strong> colour turning stage.<br />
Post-harvest treatments<br />
There are several possible treatments that can be used to extend <strong>the</strong> shelf life of<br />
harvested fruits. These include cleaning, dipping in cold water to remove field<br />
heat, treatment with chemicals such as calcium compounds, anti-oxidants,<br />
growth regulators <strong>and</strong> fungicides.<br />
Dipping <strong>the</strong> fruits in cold water <strong>for</strong> two hours or exposing to cold air <strong>for</strong> four<br />
hours immediately after harvest to remove field heat has been shown to prolong<br />
shelf life.<br />
Dipping <strong>the</strong> fruits in a solution of calcium chloride (1 to 2 %) containing a<br />
surfactant can prolong <strong>the</strong> shelf life of ber fruits by delaying <strong>the</strong> onset of<br />
ripening.<br />
Post-harvest dipping of fruits into a solution of ascorbic acid (150 to 300 ppm<br />
ascorbic acid) can reduce over-ripening <strong>and</strong> increase <strong>the</strong> levels of TSS.<br />
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However, this treatment has no effect on <strong>the</strong> acidity or ascorbic acid content of<br />
<strong>the</strong> fruit.<br />
Dipping <strong>the</strong> fruits (Gola cultivar) in a solution (1000 ppm) of potassium<br />
permanganate (KMnO 4 ) at <strong>the</strong> colour turning stage gave <strong>the</strong> best result of<br />
extending <strong>the</strong> shelf life of fruits to 14 days at room temperature (Ramkrishan<br />
Godara, 1994). Also, Umran fruits harvested at <strong>the</strong> golden yellow colour stage<br />
<strong>and</strong> dipped in a solution of 10 ppm benzyl adenine <strong>for</strong> five minutes, <strong>the</strong>n<br />
packed in polyethylene bags, had a lower weight loss, higher TSS, sugars <strong>and</strong><br />
ascorbic acid <strong>and</strong> a greater palatability rating after storage <strong>for</strong> eight days<br />
(S<strong>and</strong>hbhor <strong>and</strong> Desai, 1991).<br />
Treatment with a range of different growth regulators has been successful at<br />
delaying <strong>the</strong> ripening of harvested fruits <strong>and</strong> maintaining <strong>the</strong> high quality of ber<br />
fruits during storage. The application of cycocel (500 ppm <strong>for</strong> 15 minutes <strong>and</strong><br />
1000 to 2000 ppm <strong>for</strong> 10 minutes), maleic hydrazide (200 ppm) <strong>and</strong><br />
benzyladenine (10 ppm <strong>and</strong> 100 ppm) have all been shown to reduce weight<br />
loss <strong>and</strong> improve <strong>the</strong> quality of stored ber fruits when stored in wooden boxes<br />
or poly<strong>the</strong>ne bags (Pareek, 2001).<br />
Spraying with a fungicide such as thiobendazole (500 ppm) or zinc sulphate<br />
(ZnSO 4 ) (0.2 %) also reduces decay of <strong>the</strong> fruit during storage. Care to follow<br />
health <strong>and</strong> safety regulations (see box) should be taken when using fungicides.<br />
Health <strong>and</strong> safety when using Thiobendazole <strong>and</strong> Zinc sulphate (ZnSO 4 )<br />
H<strong>and</strong>ling <strong>and</strong> storage:<br />
Store <strong>the</strong> material in a well ventilated, secure area out of reach of children <strong>and</strong><br />
domestic animals. Do not store food, beverages or tobacco products in <strong>the</strong><br />
storage area. Prevent eating, drinking <strong>and</strong> tobacco use in areas where <strong>the</strong>re is a<br />
potential <strong>for</strong> exposure to <strong>the</strong> material. Wear protective clothing <strong>and</strong> avoid<br />
contact with <strong>the</strong> skin <strong>and</strong> eyes .Where eye contact is likely, use chemical splash<br />
goggles. Wash thoroughly with soap <strong>and</strong> water after h<strong>and</strong>ling.<br />
Environmental impact:<br />
Thiobendazole: Very toxic to aquatic organisms<br />
ZnSO 4 : no ecological problems are expected when <strong>the</strong> product is h<strong>and</strong>led <strong>and</strong><br />
used with care.<br />
Wax treatment<br />
Coating with wax has been shown to be effective at retaining <strong>the</strong> physical<br />
appearance of Umran fruits, but had no effect on <strong>the</strong>ir organoleptic quality.<br />
After dipping fruits in Waxol-O-12 <strong>for</strong> 30 seconds, <strong>the</strong>y remained in good<br />
125
condition <strong>for</strong> 30 to 40 days when kept in poly<strong>the</strong>ne bags <strong>and</strong> stored at 0-3.3° C.<br />
At room temperature, <strong>the</strong>y could only be stored <strong>for</strong> 12 days. Fruits coated in<br />
paraffin wax (2 %) <strong>and</strong> treated with 10 ppm NAA or 100 ppm ascorbic acid<br />
could be stored <strong>for</strong> 12 days at room temperature <strong>and</strong> up to 18 days when <strong>the</strong><br />
temperature was reduced to 10-12° C.<br />
Wax coated fruits must be washed properly be<strong>for</strong>e use.<br />
Irradiation of fruits<br />
Radiation preservation of ber fruits is one post-harvest strategy that may help to<br />
delay post-harvest ripening <strong>and</strong> senescence <strong>and</strong> <strong>the</strong>reby reduce losses <strong>and</strong><br />
extend <strong>the</strong> shelf life of fruits. Studies carried out on <strong>the</strong> use of irradiation on ber<br />
have been found to be encouraging. Ahmed et al. (1972) treated mature hard,<br />
green ber fruits of cultivar Umran-13 with 10, 20, 30, 40 <strong>and</strong> 50 k rad of<br />
gamma rays. They found that those fruits treated with 20 to 40 k rad doses were<br />
relatively firmer <strong>and</strong> greener than <strong>the</strong> controls during a subsequent storage<br />
period of eight days at room temperature (30 ± 2° C). Irradiation had no<br />
detectable adverse effects on <strong>the</strong> taste <strong>and</strong> flavour of ripened fruits, or on <strong>the</strong><br />
chemical composition of <strong>the</strong> fruit.<br />
9.2.3 Processing<br />
In India <strong>the</strong> ripe ber fruits are mostly consumed raw, but are sometimes stewed.<br />
In Sou<strong>the</strong>ast Asia, <strong>the</strong> unripe fruits are often eaten with salt.<br />
<strong>Ber</strong> fruits are used to make a number of different products. One of <strong>the</strong> simplest<br />
<strong>for</strong>ms of processing is dehydration, which is essential <strong>for</strong> prolonged storage of<br />
<strong>the</strong> fruit. The dried ripe fruits are sometimes ground into a powder <strong>for</strong><br />
prolonged storage <strong>and</strong> out-of-season use. Both dried <strong>and</strong> fresh ber can be used<br />
<strong>for</strong> fur<strong>the</strong>r processing. Slightly under-ripe fruits are c<strong>and</strong>ied by a process of<br />
pricking, immersing in a salt solution that gradually increases from 2 to 8 %,<br />
draining, immersing in an<strong>o<strong>the</strong>r</strong> solution of 8 % salt <strong>and</strong> 0.2 % potassium<br />
metabisulphite, storing <strong>for</strong> one to three months, rinsing <strong>and</strong> cooking in sugar<br />
syrup with citric acid. Acidic types of fruit are used <strong>for</strong> pickling or chutneys. In<br />
Africa, <strong>the</strong> dried <strong>and</strong> fermented pulp is pressed into cakes that are similar to<br />
gingerbread. In Venezuela a liqueur is made from <strong>the</strong> fruits <strong>and</strong> sold as ‘Crema<br />
de ponsigue’.<br />
Traditionally, ber fruits are washed, drained <strong>and</strong> sun dried. The quality of <strong>the</strong><br />
dried product varies according to <strong>the</strong> different varieties of ber, <strong>the</strong> level of<br />
maturity at harvest <strong>and</strong> <strong>the</strong> environmental <strong>and</strong> physical conditions during<br />
dehydration. See flow chart 1 <strong>for</strong> an outline of <strong>the</strong> ber dehydration process. The<br />
quality of dried product from different cultivars varies. Fruits of <strong>the</strong> cultivars<br />
Katha or Umran, Bagwadi, Chhuhura, Mehrun, Sanaur-2, Sanaur-3, Sanaur-4,<br />
Illaicji <strong>and</strong> Karaka all give a good dehydrated product. In general, <strong>the</strong> quality is<br />
better from varieties of Umran or Katha <strong>and</strong> Chhuhura, although some<br />
126
consumers prefer <strong>the</strong> more acidic fruits of Sanaur-2, Sanaur-3, Sanaur-4 <strong>and</strong><br />
Mehrun.<br />
The stage of maturity of <strong>the</strong> fruit also determines <strong>the</strong> quality <strong>and</strong> recovery of<br />
<strong>the</strong> dehydrated product. Recovery of <strong>the</strong> dried product is greater when ripe, but<br />
firm ra<strong>the</strong>r than mature fruits are used. Golden yellow to reddish brown fruits<br />
give <strong>the</strong> best quality of dehydrated product.<br />
Pre-treatments such as blanching (dipping <strong>the</strong> fruit in boiling water <strong>for</strong> 2-6<br />
minutes) <strong>and</strong> sulphuring be<strong>for</strong>e dehydration improve <strong>the</strong> product quality.<br />
Blanching induces <strong>the</strong> development of a uni<strong>for</strong>m yellow colour, stops <strong>the</strong><br />
activity of enzymes <strong>and</strong> micro-organisms that cause spoilage <strong>and</strong> softens <strong>the</strong><br />
fruit so that dehydration takes place at a uni<strong>for</strong>m rate. The optimum time <strong>for</strong><br />
blanching varies between cultivars <strong>and</strong> is dependent upon <strong>the</strong> size of <strong>the</strong> fruit<br />
<strong>and</strong> softness of <strong>the</strong> pulp (see Table 9.5).<br />
Table 9.5 Optimum blanching times <strong>for</strong> ber cultivars<br />
Cultivar<br />
Blanching time<br />
(minutes)<br />
Illaichi 2<br />
Bagwadi 4<br />
Karaka <strong>and</strong> Umran 6<br />
After blanching, <strong>the</strong> fruits can be sulphured. This process helps to preserve <strong>the</strong><br />
colour of <strong>the</strong> dried ber <strong>and</strong> retain some of <strong>the</strong> ascorbic acid content. Sulphuring<br />
is an optional step <strong>and</strong> depends upon <strong>the</strong> final market <strong>for</strong> <strong>the</strong> fruit. Fruits are<br />
sulphured by exposing <strong>the</strong>m to <strong>the</strong> fumes of sulphur dioxide, which is<br />
generated by burning sulphur powder (3.5 to 10 g per kg fruit) in an enclosed<br />
chamber or sulphur tent.<br />
The quality of dried ber is also dependent upon <strong>the</strong> drying methods <strong>and</strong><br />
conditions. Traditionally drying is carried out by spreading <strong>the</strong> fruits on <strong>the</strong><br />
floor, on mats or on poly<strong>the</strong>ne sheets <strong>and</strong> leaving in <strong>the</strong> sun <strong>for</strong> 7 to 10 days.<br />
The quality of <strong>the</strong>se fruit depends on <strong>the</strong> local wea<strong>the</strong>r <strong>and</strong> sanitary conditions.<br />
Usually a fairly good product is obtained by sun drying. The quality of <strong>the</strong><br />
dried product can be improved by using a solar cabinet, which reduces <strong>the</strong><br />
number of days taken to dry <strong>the</strong> product to about four or five.<br />
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Sulphuring<br />
Sulphur dioxide is sometimes used as an additional <strong>for</strong>m of preservative when<br />
drying fruits. The addition of sulphur dioxide improves <strong>the</strong> colour <strong>and</strong><br />
increases <strong>the</strong> shelf life of <strong>the</strong> dried ber. There are two main methods of<br />
applying sulphur dioxide (SO 2 ) to fruits:<br />
<br />
<br />
by burning elemental sulphur in a sulphur cabinet or tent<br />
by soaking fruits in a solution of sodium sulphite, sodium metabisulphite<br />
or potassium metabisulphite.<br />
The strength of <strong>the</strong> sulphite solution or <strong>the</strong> amount of sulphur used <strong>and</strong> <strong>the</strong><br />
time of exposure, depend on <strong>the</strong> commodity, its moisture content <strong>and</strong> <strong>the</strong><br />
residual levels permitted in <strong>the</strong> final product, which are set by legal st<strong>and</strong>ards<br />
in each country. Typically a 3 g per litre solution of sulphite or 2 g of sulphur<br />
<strong>for</strong> each kg of prepared fruit is used. The sulphuring time varies from 1 to 3<br />
hours <strong>and</strong> is dependent upon <strong>the</strong> size <strong>and</strong> texture of <strong>the</strong> fruit being sulphured.<br />
The permitted levels <strong>for</strong> use are 0.005 to 0.2 % concentration in dried fruits. If<br />
too much sulphite is used, it taints <strong>the</strong> fruit.<br />
Importers in <strong>the</strong> European Union <strong>and</strong> United States of America may specify<br />
that sulphur dioxide is not used <strong>for</strong> <strong>the</strong> products.<br />
Sulphuring is an optional stage during <strong>the</strong> drying of ber fruits. Its use really<br />
depends upon <strong>the</strong> facilities available <strong>for</strong> sulphuring <strong>and</strong> <strong>the</strong> intended end use<br />
of <strong>the</strong> dried fruit. When ber fruits are dried <strong>for</strong> home preservation, it is not<br />
usually economically feasible to include sulphuring as part of <strong>the</strong> process.<br />
After dehydration, <strong>the</strong> fruits should be packaged in moisture-proof containers,<br />
e.g. 400 gauge food grade poly<strong>the</strong>ne bags or airtight tins. The dried product can<br />
be used <strong>for</strong> a dessert or it can be reconstituted in a 10 % sugar solution <strong>and</strong><br />
consumed as a liquid beverage.<br />
Sun-drying is <strong>the</strong> simplest <strong>and</strong> cheapest <strong>for</strong>m of drying fruits. However, it is<br />
very wea<strong>the</strong>r dependent <strong>and</strong> does not always produce <strong>the</strong> highest quality dried<br />
fruit. There are various driers that could be used to improve <strong>the</strong> quality of <strong>the</strong><br />
product, but <strong>the</strong>ir use very much depends on <strong>the</strong> intended use of <strong>the</strong> fruit. High<br />
value fruits would be dried using mechanical driers. Unless <strong>the</strong>re is a market<br />
<strong>for</strong> high quality dried ber fruit, it would not be economically viable to use an<br />
improved <strong>for</strong>m of drying.<br />
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Flow chart 1. The preparation of dehydrated ber<br />
Process Process notes + quality control<br />
Graded, ripe Only use ripe, firm fruits without marks or bruising. Golden<br />
fruits yellow to reddish brown fruits give <strong>the</strong> best quality.<br />
Wash <strong>and</strong> Wash in clean water. Remove any leaves, twigs <strong>and</strong> <strong>o<strong>the</strong>r</strong><br />
sort<br />
material.<br />
Blanch fruits Blanch fruits by plunging <strong>the</strong>m in boiling water <strong>for</strong> 2 to 6<br />
minutes.<br />
Sulphur fruits Fruit is ei<strong>the</strong>r sulphured using SO 2 gas or sulphited by dipping<br />
(optional) in a solution of sodium metabisulphite:<br />
1. Create a chamber in which <strong>the</strong> sulphur powder (3.5 to 10<br />
g/kg fruit) can be burned. The chamber must be airtight to<br />
prevent <strong>the</strong> fumes from escaping. The chamber can be made<br />
from a large cardboard box or from a poly<strong>the</strong>ne tent. Wooden<br />
sulphur cabinets are available <strong>for</strong> purchase. Place <strong>the</strong> fruit in<br />
single layers on trays inside <strong>the</strong> chamber. Burn <strong>the</strong> sulphur at<br />
<strong>the</strong> base of <strong>the</strong> chamber, away from <strong>the</strong> side of <strong>the</strong> box. Leave<br />
<strong>the</strong> fruit in <strong>the</strong> chamber <strong>for</strong> up to 3 hours.<br />
2. Make a solution of sodium sulphite or sodium<br />
metabisulphite (3 g sodium per litre water). Dip <strong>the</strong> fruits into<br />
<strong>the</strong> solution <strong>for</strong> 60 to 90 minutes.<br />
Place on Place <strong>the</strong> fruit in a single layer on mesh trays. The fruits<br />
mesh trays<br />
Dry<br />
Package <strong>and</strong><br />
seal<br />
Label<br />
(optional)<br />
Store<br />
should be as close toge<strong>the</strong>r as possible, but not touching.<br />
There are several options <strong>for</strong> drying, depending on <strong>the</strong><br />
facilities available, <strong>the</strong> value of <strong>the</strong> product <strong>and</strong> <strong>the</strong> intended<br />
end use.<br />
a. Sun drying. Dry under <strong>the</strong> bright sun <strong>for</strong> 7 to 10 days until<br />
dry. Turn <strong>the</strong> fruits over daily.<br />
b. Solar drying. Place fruits in a solar drier <strong>for</strong> 4 to 5 days<br />
until dried.<br />
c. Cabinet drier. Place <strong>the</strong> fruits in a cabinet drier at 60-65°<br />
C <strong>for</strong> 20 to 30 hours until dry.<br />
For all drying methods, <strong>the</strong> final moisture content of dried<br />
fruits should be 15 %. The fruits will have a soft rubbery<br />
texture. With experience, processors will know when dried ber<br />
have reached <strong>the</strong> correct moisture level.<br />
Pack <strong>the</strong> dried fruits in moisture-proof containers e.g. 400<br />
gauge poly<strong>the</strong>ne or polypropylene pouches <strong>and</strong> heat seal <strong>the</strong>m.<br />
Fruits that are being dried <strong>for</strong> home storage should be<br />
transferred to storage sacks.<br />
If fruits are being dried <strong>for</strong> sale, <strong>the</strong> packages should be<br />
labelled. Label with <strong>the</strong> product name <strong>and</strong> date of drying.<br />
Dried fruits should be stored in a dry, cool environment, away<br />
from pests <strong>and</strong> animals <strong>and</strong> away from chemicals which may<br />
contaminate <strong>the</strong> product.<br />
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9.2.3.1 <strong>Ber</strong> preserve<br />
Mature fruits can be used to make a preserve, known locally in India as<br />
murabba. Fruits of <strong>the</strong> cultivars Umran, Banarsi, Karaka <strong>and</strong> Kaithli are <strong>the</strong><br />
best <strong>for</strong> <strong>the</strong> preparation of preserve (Pareek, 2001).<br />
The best preserve is made from fully mature fruits that are at <strong>the</strong> hard stage.<br />
Ripe fruits are not suitable since <strong>the</strong> structure will be too soft.<br />
After washing <strong>and</strong> sorting <strong>the</strong> fruits, <strong>the</strong> skins need to be pricked so that sugar<br />
can impregnate <strong>the</strong> fruit. They are ei<strong>the</strong>r pricked with a <strong>for</strong>k or by using a<br />
pricking board or pricking machine, similar to <strong>the</strong> one that is used <strong>for</strong> pricking<br />
olives. The pricked fruits <strong>the</strong>n need to be softened. One method of softening<br />
<strong>the</strong> fruits is to soak <strong>the</strong>m in brine solutions of gradually increasing<br />
concentration. For example, 2 % brine <strong>for</strong> <strong>the</strong> first day, 4 % brine <strong>the</strong> second<br />
day, 6 % brine on <strong>the</strong> third day <strong>and</strong> <strong>the</strong>n 8 % brine solution <strong>for</strong> one to three<br />
months. However, this method proved to be too time consuming <strong>and</strong> it was<br />
difficult to remove all traces of salt from <strong>the</strong> fruit (Pareek, 2001). There<strong>for</strong>e<br />
alternative methods of softening have been used.<br />
A simpler method of softening <strong>the</strong> fruit is to blanch <strong>the</strong> pricked fruits by<br />
plunging <strong>the</strong>m into boiling water <strong>for</strong> anything from 2 to 190 minutes depending<br />
upon <strong>the</strong> cultivar, stage of maturity <strong>and</strong> size of fruit. After blanching, <strong>the</strong> fruits<br />
are dipped in cold water to stop <strong>the</strong> process.<br />
At this stage, <strong>the</strong> fruit can be peeled if desired, by using a pectinase enzyme<br />
(fruits are dipped in a solution of 2.5 % pectinase enzyme <strong>for</strong> 72 hours). This is<br />
an optional stage.<br />
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Flow chart 2. The preparation of ber preserve<br />
Process<br />
Graded ripe fruits<br />
Wash <strong>and</strong> sort<br />
Prick<br />
Blanch<br />
Rinse<br />
De-stone (optional)<br />
Impregnate with sugar<br />
Remove fruit from <strong>the</strong><br />
syrup <strong>and</strong> increase <strong>the</strong><br />
strength of sugar syrup<br />
Increase <strong>the</strong> strength of<br />
sugar syrup<br />
Bottle<br />
Process notes + quality control<br />
Only use fully mature fruits at <strong>the</strong> hard stage.<br />
Wash fruits in clean water. Discard bruised <strong>and</strong><br />
over-ripe fruits.<br />
Prick <strong>the</strong> skin to improve <strong>the</strong> uptake of sugar. A<br />
<strong>for</strong>k can be used or a pricking board.<br />
Plunge into boiling water <strong>for</strong> 2 to 10 minutes<br />
depending upon cultivar, stage of maturity <strong>and</strong><br />
size of fruit.<br />
Dip in cold water to stop <strong>the</strong> blanching process.<br />
Remove <strong>the</strong> stones from <strong>the</strong> centre of <strong>the</strong> fruits<br />
using a cork borer.<br />
Submerge overnight in 30° Brix sugar syrup <strong>and</strong><br />
add 0.5 % citric acid.<br />
Slowly increase <strong>the</strong> strength of <strong>the</strong> sugar syrup.<br />
Add 250 g sugar per kg fruit to <strong>the</strong> syrup. Boil<br />
<strong>for</strong> a few minutes. Cool to room temperature <strong>and</strong><br />
replace <strong>the</strong> fruits in <strong>the</strong> syrup. Leave to soak <strong>for</strong><br />
two days.<br />
Repeat <strong>the</strong> above step twice more until <strong>the</strong> final<br />
sugar content is 65 to 70° Brix. Leave to<br />
equalise <strong>for</strong> about two days.<br />
Pour <strong>the</strong> fruits <strong>and</strong> 70° Brix syrup into sterilised<br />
bottles. Seal <strong>and</strong> label.<br />
Fruits can also be de-stoned if desired. This is an optional step <strong>and</strong> depends on<br />
<strong>the</strong> consumer dem<strong>and</strong> <strong>and</strong> taste.<br />
The softened fruits are <strong>the</strong>n ready <strong>for</strong> impregnation with sugar. This is achieved<br />
by submerging <strong>the</strong> fruits in a solution of sugar syrup. The concentration of <strong>the</strong><br />
sugar syrup is gradually increased while <strong>the</strong> fruits soak. On day one, <strong>the</strong> fruits<br />
are immersed in a sugar syrup of 30° Brix. Citric acid (0.5 %) is added to <strong>the</strong><br />
syrup to help maintain <strong>the</strong> colour of <strong>the</strong> fruit <strong>and</strong> to reduce <strong>the</strong> pH of <strong>the</strong> syrup.<br />
This gives a slightly acidic taste to <strong>the</strong> product, <strong>and</strong> also helps to prevent<br />
fermentation of <strong>the</strong> fruit during <strong>the</strong> soaking period. It is possible to start <strong>the</strong><br />
soaking process with a stronger sugar syrup (say of 50° Brix), but experience<br />
has shown that <strong>the</strong> fruits are liable to shrink when a high concentration is used<br />
from <strong>the</strong> start as water is drawn out of <strong>the</strong> fruit too quickly. The principle of<br />
this method of preservation is that water is drawn out of <strong>the</strong> fruit by osmosis. It<br />
is best if this happens at a slow rate. As <strong>the</strong> water is drawn out of <strong>the</strong> fruit, <strong>the</strong><br />
sugar content (<strong>the</strong> total soluble solids content) of <strong>the</strong> fruit increases. The water<br />
that is drawn out of <strong>the</strong> fruit into <strong>the</strong> surrounding syrup dilutes <strong>the</strong> sugar syrup,<br />
131
<strong>the</strong>re<strong>for</strong>e it is necessary to keep adding more sugar to <strong>the</strong> syrup to increase <strong>the</strong><br />
concentration of <strong>the</strong> syrup. Water will continue to be removed from <strong>the</strong> fruit<br />
until <strong>the</strong> total soluble solids content of <strong>the</strong> fruit reaches about 70° Brix<br />
measured using a refractometer.<br />
There are many different methods of preserving ber, <strong>and</strong> <strong>the</strong>y differ in <strong>the</strong><br />
length of time it takes to reach <strong>the</strong> end point at 70 % total solids. The following<br />
method is one that is recommended by Khurdiya <strong>and</strong> Singh, (1975):<br />
Day 1. Immerse <strong>the</strong> fruits in a 30° Brix sugar solution. Add 0.5 % citric acid<br />
<strong>and</strong> leave overnight.<br />
Day 2. Remove <strong>the</strong> fruits from <strong>the</strong> syrup, add sugar (about 250 g/kg fruit) to<br />
<strong>the</strong> syrup <strong>and</strong> boil to dissolve <strong>the</strong> sugar. Allow <strong>the</strong> syrup to cool <strong>and</strong> replace <strong>the</strong><br />
fruits into it. Leave <strong>for</strong> two days.<br />
Day 4. Remove <strong>the</strong> fruits from <strong>the</strong> syrup, add sugar (about 250 g/kg fruit) to<br />
<strong>the</strong> syrup <strong>and</strong> boil to dissolve <strong>the</strong> sugar. Allow <strong>the</strong> syrup to cool <strong>and</strong> replace <strong>the</strong><br />
fruits into it. Leave <strong>for</strong> two days<br />
Day 6. Remove <strong>the</strong> fruits from <strong>the</strong> syrup, add sugar (about 250 g/kg fruit) to<br />
<strong>the</strong> syrup <strong>and</strong> boil to dissolve <strong>the</strong> sugar. Allow <strong>the</strong> syrup to cool <strong>and</strong> replace <strong>the</strong><br />
fruits into it. Leave <strong>for</strong> two days.<br />
Day 8. Measure <strong>the</strong> TSS of <strong>the</strong> product. It should be between 65 <strong>and</strong> 70° Brix.<br />
Bottle <strong>the</strong> preserved fruit in <strong>the</strong> 70° Brix syrup. The total soluble solids (TSS)<br />
content of <strong>the</strong> fruits becomes equalised at 65 to 70° Brix.<br />
9.2.3.2 <strong>Ber</strong> c<strong>and</strong>y<br />
Mature ber fruits can also be used to make c<strong>and</strong>ied ber. Fruits of <strong>the</strong> cultivar<br />
Illaichi have <strong>the</strong> best organoleptic properties <strong>for</strong> c<strong>and</strong>y making. Kaithli,<br />
Kathaphal, Umran <strong>and</strong> Narma are also good cultivars <strong>for</strong> c<strong>and</strong>y making. Fruits<br />
should have a high total soluble solids (TSS) content, low acidity <strong>and</strong> be of<br />
average size (Pareek, 2001).<br />
The best c<strong>and</strong>y is made from fully mature fruits that are at <strong>the</strong> hard stage. Ripe<br />
fruits are not suitable since <strong>the</strong>y may be too soft.<br />
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Flow sheet 3. The preparation of ber c<strong>and</strong>y<br />
Process<br />
Graded ripe fruits<br />
Wash <strong>and</strong> sort<br />
Prick<br />
Blanch<br />
Rinse<br />
De-stone (optional)<br />
Impregnate with sugar<br />
Remove fruit from <strong>the</strong><br />
syrup <strong>and</strong> increase <strong>the</strong><br />
strength of sugar syrup<br />
Increase <strong>the</strong> strength of<br />
sugar syrup<br />
Leave to impregnate<br />
Drain<br />
Dry<br />
Roll in sugar (optional)<br />
Pack<br />
Process notes + quality control<br />
Only use fully mature fruits at <strong>the</strong> hard stage.<br />
Wash fruits in clean water. Discard bruised <strong>and</strong><br />
over-ripe fruits.<br />
Prick <strong>the</strong> skin to improve <strong>the</strong> uptake of sugar. A<br />
<strong>for</strong>k can be used or a pricking board.<br />
Plunge into boiling water <strong>for</strong> 2 to 10 minutes<br />
depending upon cultivar, stage of maturity <strong>and</strong><br />
size of fruit.<br />
Dip in cold water to stop <strong>the</strong> blanching process.<br />
Remove <strong>the</strong> stones from <strong>the</strong> centre of <strong>the</strong> fruits<br />
using a cork borer.<br />
Submerge overnight in 30° Brix sugar syrup <strong>and</strong><br />
add 0.5 % citric acid.<br />
Slowly increase <strong>the</strong> strength of <strong>the</strong> sugar syrup.<br />
Add 250 g sugar per kg fruit to <strong>the</strong> syrup. Boil <strong>for</strong><br />
a few minutes. Cool to room temperature <strong>and</strong><br />
replace <strong>the</strong> fruits in <strong>the</strong> syrup. Leave to soak <strong>for</strong><br />
two days.<br />
Repeat <strong>the</strong> above step twice more until <strong>the</strong> final<br />
sugar content is 65 to 70° Brix. Leave to equalise<br />
<strong>for</strong> about two days.<br />
Leave <strong>the</strong> fruits in <strong>the</strong> 65-70° Brix sugar solution<br />
<strong>for</strong> 10 to 25 days.<br />
Remove <strong>the</strong> fruits from <strong>the</strong> syrup <strong>and</strong> drain on<br />
wire mesh trays.<br />
Dry <strong>the</strong> drained fruits in <strong>the</strong> sun or in a warm<br />
room until <strong>the</strong>y reach a final moisture content of<br />
10-15 %.<br />
Roll <strong>the</strong> dried fruits in sugar powder to make<br />
crystallised fruits.<br />
Package in moisture-proof containers such as tins,<br />
jars or poly<strong>the</strong>ne pouches.<br />
The process <strong>for</strong> making c<strong>and</strong>ied ber fruits is essentially <strong>the</strong> same as <strong>for</strong> making<br />
ber preserve outlined above. <strong>Ber</strong> fruits are submerged in sugar syrups of slowly<br />
increasing strength until a final concentration of 70° Brix is reached. At this<br />
point, <strong>the</strong> fruits are left to soak in <strong>the</strong> 70° Brix syrup <strong>for</strong> a fur<strong>the</strong>r ten to twenty<br />
five days. After this time, <strong>the</strong> fruits are taken from <strong>the</strong> syrup <strong>and</strong> spread on wire<br />
fruit trays <strong>for</strong> <strong>the</strong> excess syrup to drain off. The drained fruits are dried in <strong>the</strong><br />
sun or in a warm room until <strong>the</strong>y reach a final moisture content of 10-15 per<br />
cent.<br />
133
As an option, dried c<strong>and</strong>ied fruits can be rolled in powdered sugar to make a<br />
crystallised product. The dried fruits should be packed in moisture-proof<br />
packets such as jars, tins or poly<strong>the</strong>ne pouches.<br />
9.2.3.3 <strong>Ber</strong> pulp<br />
<strong>Ber</strong> fruits can be partially processed into a pulp that has a relatively long shelf<br />
life of up to six months. This pulp can be used to make a range of products<br />
including squash, jam, fruit beverage, fruit nectar, chutney, pickle <strong>and</strong> fruit<br />
lea<strong>the</strong>r. The advantage of making fruit pulp is to extend <strong>the</strong> period of<br />
availability of ber <strong>for</strong> processing into fur<strong>the</strong>r products. Thus, <strong>the</strong> processing<br />
season <strong>for</strong> jams, chutneys etc. can be spread out over a longer period.<br />
<strong>Ber</strong> fruits are processed into pulp at times when <strong>the</strong>re is a glut of fruit. Juicy<br />
varieties of ber are <strong>the</strong> best type <strong>for</strong> making pulp, but most varieties can be<br />
used.<br />
The fruits are de-stoned <strong>and</strong> cut into small pieces. These pieces are heated with<br />
water (2 parts fruit to 1 part water) <strong>for</strong> a few minutes to soften <strong>the</strong> flesh <strong>and</strong><br />
<strong>the</strong>n passed though a stainless steel sieve or through a pulping machine to <strong>for</strong>m<br />
a smooth pulp or puree. Sodium metabisulphite (1.2-1.5 g/kg pulp) is added to<br />
<strong>the</strong> pulp as a preservative. The pulp is packaged in sterile sealed containers <strong>and</strong><br />
stored <strong>for</strong> use at a later date. Treated like this, <strong>the</strong> pulp will have a shelf life of<br />
up to 6 months depending on storage conditions <strong>and</strong> hygiene during <strong>the</strong><br />
preparation. When <strong>the</strong> pulp is used, it should be heated well to liberate some of<br />
<strong>the</strong> sulphur dioxide gas <strong>and</strong> reduce levels to those which are legally acceptable.<br />
9.2.3.4 <strong>Ber</strong> chutney<br />
Dried ber, fresh fruits or pulp can be used to prepare a spicy fruit chutney (see<br />
box <strong>for</strong> ingredients). In <strong>the</strong> following example from Bangladesh, dried fruit is<br />
used. After cleaning <strong>and</strong> sorting, <strong>the</strong> fruit is soaked overnight in water to<br />
rehydrate it. Usually this length of time is sufficient to soften <strong>the</strong> fruit but if any<br />
remains hard after soaking, <strong>the</strong> fruit should be heated. The soaked fruit is<br />
removed from <strong>the</strong> soaking water, rinsed <strong>and</strong> placed in a pan with sugar at 700 g<br />
to 1 kg per kg dried fruit, according to taste. The ber <strong>and</strong> sugar are stirred to<br />
dissolve <strong>the</strong> fruit <strong>and</strong> <strong>the</strong>n heated <strong>for</strong> 10 to 15 minutes until <strong>the</strong> total soluble<br />
solids content is 55° Brix, measured with a refractometer. Spices such as chilli<br />
powder, cumin, aniseed, ground cinnamon, ground nutmeg <strong>and</strong> black pepper<br />
are dry roasted in a heavy iron pan be<strong>for</strong>e use. They are <strong>the</strong>n added, toge<strong>the</strong>r<br />
with mustard powder, to <strong>the</strong> heated ber fruits, stirred well to mix <strong>and</strong> heated.<br />
Acetic acid (vinegar) <strong>and</strong> salt are added, stirred well to mix <strong>and</strong> heated again.<br />
Heating is continued until <strong>the</strong> TSS reaches 60° Brix. The chutney is <strong>the</strong>n ready<br />
<strong>for</strong> bottling. A preservative, potassium or sodium metabisulphite (KMS or<br />
NaMS) can be added as an option at this stage if desired.<br />
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Ingredients <strong>for</strong> ber chutney<br />
1 kg dried ber<br />
700 g -1 kg sugar depending upon cultivar <strong>and</strong> taste<br />
5 g chilli powder<br />
10 g mustard powder<br />
2 g cumin<br />
2 g aniseed<br />
2 g cinnamon<br />
1 g cardamom<br />
1 g nutmeg<br />
1 g black pepper<br />
5 ml acetic acid<br />
30 g salt<br />
2 g potassium metabisulphite (KMS) (optional)<br />
The amount of spices used can be varied according to local taste <strong>and</strong> preference<br />
The chemical helps to preserve <strong>the</strong> chutney <strong>and</strong> protect against fungal damage.<br />
However, some consumers prefer to buy a product that is free from<br />
preservatives. Preservatives are not an essential component of a chutney. When<br />
a chutney is prepared correctly, <strong>the</strong> combination of a high sugar content <strong>and</strong> a<br />
high level of acidity (from using vinegar) should be sufficient to preserve <strong>the</strong><br />
product.<br />
Some processors choose to add <strong>the</strong> preservative as an added measure of<br />
caution, especially when <strong>the</strong> products are being made at <strong>the</strong> small scale <strong>and</strong> are<br />
likely to be stored in humid environments. Adding preservative such as KMS<br />
should never be seen as an alternative to observing good hygienic practice <strong>and</strong><br />
following <strong>the</strong> correct production method.<br />
The method <strong>for</strong> producing ber chutney, toge<strong>the</strong>r with <strong>the</strong> quality control steps,<br />
is included in flow chart 4.<br />
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Flow chart 4. The preparation of ber chutney<br />
Process<br />
Dried ber fruit<br />
Soak in clean<br />
water<br />
Add sugar<br />
Heat<br />
Dry roast spices<br />
Add spices<br />
Heat<br />
Add acetic acid<br />
<strong>and</strong> salt<br />
Heat<br />
Add preservative<br />
(optional)<br />
Bottle<br />
Process notes + quality control<br />
Select 1 kg dried ber fruit.<br />
Soak overnight to soften <strong>the</strong> fruit. If it remains hard after<br />
about 12 hours soaking, heat gently until all fruit is<br />
softened.<br />
700 g-1kg per kg dried fruit depending upon local taste.<br />
Heat <strong>the</strong> mixture <strong>for</strong> about 10 to 15 minutes until <strong>the</strong><br />
mixture thickens <strong>and</strong> <strong>the</strong> TSS is 55 Brix.<br />
Dry roast <strong>the</strong> spices (chilli powder, cumin, aniseed, ground<br />
cinnamon, ground nutmeg <strong>and</strong> black pepper) on a heavy<br />
iron pan.<br />
Add <strong>the</strong> roasted ground spices <strong>and</strong> <strong>the</strong> mustard powder to<br />
<strong>the</strong> chutney. Mix well.<br />
Stir well <strong>and</strong> continue to heat.<br />
Add acetic acid (vinegar) <strong>and</strong> salt to <strong>the</strong> chutney. Mix well.<br />
Continue heating until <strong>the</strong> chutney has a TSS of 60 Brix.<br />
Disperse <strong>the</strong> KMS in a little hot water. Add to <strong>the</strong> chutney,<br />
stir well to mix.<br />
Pour into clean sterile glass jars. Cap <strong>and</strong> label.<br />
9.2.3.5 <strong>Ber</strong> beverage<br />
Fresh ripe ber fruits can be used <strong>for</strong> <strong>the</strong> preparation of a fruit beverage. The<br />
juicy varieties of ber make <strong>the</strong> best juice. The fruits are washed <strong>and</strong> de-stoned<br />
<strong>the</strong>n <strong>the</strong> flesh is cut into small pieces. The fruit pieces are boiled with water (1<br />
litre of water per kg fruit pieces) <strong>for</strong> 20 to 30 minutes until <strong>the</strong> fruits are<br />
softened. The fruit pulp is passed through a stainless steel sieve or strained<br />
through a muslin juice bag to produce a clear juice. The juice is sweetened by<br />
adding sugar (500 g per litre of extracted juice), acidified by adding citric acid<br />
(10 g per litre juice extract) <strong>and</strong> diluted with clean water (2.5 litres water per<br />
litre of juice extract). The ber juice mixture is <strong>the</strong>n boiled <strong>for</strong> 5 to 10 minutes<br />
<strong>and</strong> filtered again through a muslin cloth. The clear juice is hot filled into presterilised<br />
bottles which are capped using a corking machine. The bottles should<br />
be filled to within about 5 cm of <strong>the</strong> top of <strong>the</strong> bottle to allow <strong>for</strong> expansion of<br />
<strong>the</strong> juice during pasteurisation. The sealed bottles are pasteurised by placing in<br />
a hot water bath (at 80-95° C) <strong>for</strong> 10 to 20 minutes depending upon <strong>the</strong> size of<br />
<strong>the</strong> bottle. The pasteurised bottles are cooled to room temperature by<br />
136
immersing in cool water – do not use cold water as this will crack <strong>the</strong> bottles.<br />
After cooling, <strong>the</strong> bottles are labelled <strong>and</strong> stored.<br />
In Zimbabwe, dried <strong>and</strong> fresh ber fruits have been used to make an alcoholic<br />
drink with 2 % alcohol. The fruits are crushed <strong>and</strong> fermented <strong>for</strong> seven days in<br />
ear<strong>the</strong>nware containers using yeast <strong>and</strong> lactic acid bacteria. Kainsa <strong>and</strong> Gupta<br />
(1979), investigated <strong>the</strong> preparation of wine from Umran cultivar of ber<br />
(Pareek, 2001). They reported that it is preferable to treat <strong>the</strong> fruit with a<br />
pectinase enzyme be<strong>for</strong>e fermentation as this gives about 9 % higher yield,<br />
higher alcohol content <strong>and</strong> a better clear <strong>and</strong> golden yellow wine colour than<br />
without pectinase enzyme.<br />
Flow chart 5. The preparation of ber beverage<br />
Process<br />
Fresh ripe fruits<br />
Wash <strong>and</strong> de-stone<br />
Cut fruits<br />
Boil with water<br />
Filter<br />
Add sugar, citric<br />
acid <strong>and</strong> water<br />
Boil<br />
Process notes + quality control<br />
Select fruits that are juicy <strong>and</strong> fully ripe, free from<br />
damage <strong>and</strong> signs of deterioration.<br />
Wash fruits in clean water <strong>and</strong> remove <strong>the</strong> stones<br />
manually.<br />
Cut <strong>the</strong> flesh into small pieces.<br />
Add water (1 litre water per kg chopped fruit) to <strong>the</strong> fruit<br />
<strong>and</strong> boil <strong>for</strong> 20-30 minutes until <strong>the</strong> fruit is soft <strong>and</strong><br />
pulpy.<br />
Pass <strong>the</strong> pulp through a stainless steel sieve or a muslin<br />
filter bag to produce a clear juice.<br />
Add sugar (500 g per litre extracted juice), citric acid (10<br />
g per litre extracted juice) <strong>and</strong> clean water (2.5 litres per<br />
litre of extracted juice). Mix well.<br />
Boil <strong>for</strong> 10 to 15 minutes to dissolve <strong>the</strong> sugar.<br />
Filter<br />
Filter through a muslin cloth to remove any impurities<br />
<strong>and</strong> sediments.<br />
Pour into bottles Hot-fill into pre-sterilised glass bottles. Leave a space of<br />
about 5 cm at <strong>the</strong> top of <strong>the</strong> bottle. Cap <strong>the</strong> bottles using a<br />
crown cork.<br />
Pasteurise Place capped bottles into a water bath of hot water (80-<br />
95° C) <strong>and</strong> leave <strong>for</strong> 10 to 20 minutes depending upon<br />
<strong>the</strong> bottle capacity.<br />
Cool<br />
Cool to room temperature by immersing in cool, not cold,<br />
water. Cool down gradually or <strong>the</strong> glass bottles will<br />
crack.<br />
Label<br />
Label <strong>the</strong> bottles <strong>and</strong> store.<br />
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9.2.3.6 <strong>Ber</strong> jam<br />
Ripe ber fruits can be used to make jam. Preserved ber pulp can also be used as<br />
<strong>the</strong> starting material <strong>for</strong> ber jam. If <strong>the</strong> pulp has been preserved with potassium<br />
metabisulphite, it is important to boil <strong>the</strong> pulp well to drive off <strong>the</strong> excess<br />
sulphur dioxide gas be<strong>for</strong>e using <strong>for</strong> jam. Sulphur dioxide is not usually used as<br />
a preservative <strong>for</strong> jam. If <strong>the</strong> correct production method is followed <strong>and</strong> <strong>the</strong> jam<br />
has a high enough sugar content <strong>and</strong> has been prepared <strong>and</strong> bottled<br />
hygienically, <strong>the</strong>re is no need to add chemical preservatives. Occasionally citric<br />
acid (or lemon juice) is added. This chemical has two purposes – to reduce <strong>the</strong><br />
pH of <strong>the</strong> fruit mixture so that <strong>the</strong> pectin can <strong>for</strong>m a gel <strong>and</strong> also as an antibacterial<br />
agent. If a preservative has to be added to <strong>the</strong> jam, ascorbic acid or<br />
benzoic acid are <strong>the</strong> usual chemicals that are used.<br />
Researchers in India investigated <strong>the</strong> benefits of adding pectin <strong>and</strong> ber fruit<br />
peel to jams prepared from fruits of two cultivars, Umran <strong>and</strong> Sannaur-6. They<br />
concluded that <strong>the</strong> jam with <strong>the</strong> best texture <strong>and</strong> taste was prepared from<br />
Umran fruits, without <strong>the</strong> peel on <strong>and</strong> with 1 % added pectin. More<br />
specifically, <strong>the</strong>y found that <strong>the</strong> best recipe <strong>for</strong> ber jam included 750 g sugar<br />
per kg pulp <strong>and</strong> with an acidity of 0.75 % (Dawney Thomas <strong>and</strong> Kulwal,<br />
2002).<br />
Ripe or slightly under-ripe fruits are <strong>the</strong> best type <strong>for</strong> jam making. Over-ripe<br />
<strong>and</strong> damaged fruits should be discarded as <strong>the</strong>y will spoil <strong>the</strong> jam. The fruits<br />
are washed in clean water <strong>and</strong> chopped into small pieces. The stones can be<br />
removed if desired, although <strong>the</strong>y will be sifted out at a subsequent stage. The<br />
fruit pieces are boiled with clean water (2 kg fruit per litre of water) <strong>for</strong> a few<br />
minutes until <strong>the</strong>y have softened. The soft fruit pulp is passed through a wire<br />
stainless steel mesh sieve to obtain a smooth pulp, free of skins <strong>and</strong> stones.<br />
Water (1 litre per kg of pulp) <strong>and</strong> sugar (725 g per kg pulp) are added to <strong>the</strong><br />
pulp <strong>and</strong> mixed well. Citric acid (8 g per kg pulp) is dissolved in a small<br />
amount of water <strong>and</strong> added to <strong>the</strong> pulp. The mixture is heated in a stainless<br />
steel pan, gently at first to dissolve <strong>the</strong> sugar <strong>and</strong> <strong>the</strong>n rapidly to reduce <strong>the</strong><br />
water content <strong>and</strong> <strong>the</strong> mixture thickens. The mixture should be stirred to<br />
prevent it sticking to <strong>the</strong> base of <strong>the</strong> pan <strong>and</strong> burning. As <strong>the</strong> jam is being<br />
heated it should be regularly tested with a refractometer to determine when <strong>the</strong><br />
total soluble solids (TSS) are 65° Brix. At this point, <strong>the</strong> jam should be<br />
removed from <strong>the</strong> heat, allowed to cool slightly to about 82-85° C <strong>and</strong> <strong>the</strong>n hotfilled<br />
into clean, sterilised jars. The jars are capped <strong>and</strong> allowed to cool to room<br />
temperature.<br />
138
Flow chart 6. Preparation of ber jam<br />
Process<br />
Ripe fruit – grade<br />
<strong>and</strong> wash<br />
Chop into small<br />
pieces <strong>and</strong> de-stone<br />
(optional)<br />
Boil fruit pieces<br />
Filter<br />
Pulp<br />
Add ingredients<br />
Heat<br />
Cool<br />
Cap <strong>and</strong> label<br />
Process notes + quality control<br />
Use fully ripe fruits from juicy varieties. Remove any<br />
over-ripe or damaged fruits. Wash in clean water.<br />
Chop <strong>the</strong> fruit into small pieces. Stones can be removed<br />
at this stage if desired, or <strong>the</strong>y can be sifted out at a<br />
later stage.<br />
Add water (2 kg fruit pieces to 1 litre of water) <strong>and</strong> boil<br />
<strong>for</strong> a few minutes to soften <strong>the</strong> fruit.<br />
Pass through a stainless steel sieve or mesh to remove<br />
<strong>the</strong> skins <strong>and</strong> stones <strong>and</strong> to obtain a smooth fruit pulp.<br />
The process can be started from this point if pre-made<br />
pulp is used as <strong>the</strong> starting material. The preserved pulp<br />
must be heated <strong>and</strong> boiled thoroughly to eliminate<br />
traces of sulphur from <strong>the</strong> KMS used as preservative.<br />
Add water (1 litre per kg pulp) <strong>and</strong> sugar (725 g per kg<br />
pulp) to <strong>the</strong> pulp <strong>and</strong> mix well.<br />
Dissolve citric acid (8 g per kg pulp) in water <strong>and</strong> add<br />
to <strong>the</strong> pulp. Mix well.<br />
Heat gently at first to dissolve <strong>the</strong> sugar, <strong>the</strong>n increase<br />
<strong>the</strong> heat <strong>and</strong> boil <strong>the</strong> mixture to reduce <strong>the</strong> moisture<br />
content. Heat until <strong>the</strong> mixture thickens <strong>and</strong> reaches a<br />
TSS of 65° Brix.<br />
Cool to about 82-85° C <strong>the</strong>n hot-fill into clean,<br />
sterilised jars.<br />
Add screw tops to <strong>the</strong> jars <strong>and</strong> label.<br />
9.3 O<strong>the</strong>r jujubes<br />
9.3.1 Ripening<br />
Harvesting is ei<strong>the</strong>r manual or by shaking <strong>the</strong> trees/shrubs. A mechanical<br />
shaker is commonly used <strong>for</strong> Chinese jujube (Anon, 1993). However such<br />
mechanical methods tend to increase <strong>the</strong> number of immature fruits harvested.<br />
This can be a constraint because green fruits of Chinese jujube do not ripen. If<br />
ga<strong>the</strong>red when white-green <strong>the</strong>y turn brown in two weeks <strong>and</strong> show a nonclimacteric<br />
ripening, <strong>the</strong> optimum temperature being 20-25° C (Kader et al.,<br />
1982).<br />
Fruits of Z. spina-christi also have climacteric ripening <strong>and</strong> <strong>the</strong> physicochemical<br />
changes have been analysed (Abbas et al., 1988, 1989; Abbas <strong>and</strong><br />
Saggar, 1989; Al-Niami et al., 1992).<br />
139
9.3.2 Treatments<br />
Exposure of fruits of Chinese jujube to ethylene (100 ppm at 20°C <strong>for</strong> four<br />
hours or dipping in 2000 ppm ethylene solution <strong>for</strong> two minutes) induces<br />
uni<strong>for</strong>m rapid ripening (Kader et al., 1982). Fruits of Z. spina-christi ripen<br />
rapidly by dipping in 5000 ppm ethaphon <strong>for</strong> one minute (Abbas et al.,1994).<br />
9.3.3 Storage<br />
Storage of fruits of <strong>o<strong>the</strong>r</strong> species at ambient temperatures is similar to that of<br />
ber. Both Chinese jujube <strong>and</strong> Z. spina-christi can be freeze-dried or frozen<br />
although vitamin C content tends to decrease (Dzheneeva <strong>and</strong> Chernogorod,<br />
1989; Al-Hijiya et al., 1989).<br />
Fumigation to remove insects is possible <strong>for</strong> jujubes; use of hydrogen<br />
phosphide <strong>for</strong> this purpose has been demonstrated <strong>for</strong> fruits of Chinese jujube<br />
intended <strong>for</strong> herbal medicines (Khalid et al., 1988).<br />
9.3.4 Processing of Chinese jujube<br />
Shin et al., (1992) investigated various processing methods <strong>for</strong> Z. jujuba fruits.<br />
Based on sensory evaluation <strong>and</strong> chemical analysis, it was found that dried<br />
fruits, nectar, jam, fruit extracts <strong>and</strong> a powdered tea were <strong>the</strong> most promising<br />
products. The processing of damaged or defective Z. jujuba fruit was<br />
investigated by Zhang et al., (2004). This is useful if mechanical harvesters<br />
increase <strong>the</strong> percentage of damaged fruits. They looked at <strong>the</strong> processing<br />
technology <strong>and</strong> parameters required <strong>for</strong> fermenting vinegar. Alcohol<br />
fermentation of vinegar was carried out using Z. jujuba fruits fermented with 8-<br />
10 % sugars <strong>and</strong> Saccharomyces ellipsodieus. Ethane acid fermentation was<br />
achieved using 5 % Acetobacter rancens. The optimum conditions <strong>for</strong><br />
clarifying <strong>the</strong> resultant Chinese jujube vinegar involved heating at 95° C <strong>for</strong><br />
two minutes, <strong>and</strong> filtering with diatomite after cooling.<br />
9.3.4.1 Jujube cake<br />
(Cali<strong>for</strong>nia Rare Fruit Growers, 1996)<br />
1 cup sugar<br />
½ cup butter<br />
2 cups dried, minced jujube<br />
cup water<br />
These are brought to <strong>the</strong> boil, <strong>the</strong>n set aside to cool<br />
2 cups wheat flour<br />
1 teaspoonful soda<br />
½ teaspoonful salt<br />
sifted toge<strong>the</strong>r <strong>and</strong> <strong>the</strong>n added to <strong>the</strong> above mixture, <strong>the</strong> whole baked at 160° C.<br />
140
141<br />
Plate 1. 30 day old<br />
rootstock seedling in<br />
polytube<br />
Plate 2. 100 day old rootstock<br />
seedling in polytube ready <strong>for</strong><br />
transplanting or budding<br />
Plate 3. Scion buds successfully<br />
sprouted
Plate 4. Rootstock prepared <strong>for</strong> patch or shield budding<br />
Plate 5. Patch <strong>and</strong> shield buds inserted on <strong>the</strong> rootstocks<br />
Plate 6. Scion buds tied after insertion<br />
142
Plate 7. Fruitfly infested ber fruits<br />
Plate 8. Twigs infested by lac insects<br />
143
Plate 9. Powdery mildew infestation on young fruits <strong>and</strong> leaves<br />
Plate 10. Alternaria leaf spot<br />
144
Plate 11. Isariopsis leaf spot<br />
Plate 12. Rust on leaves<br />
Plate 13. Alternaria fruit spot<br />
145
Plate 14. Chinese date <strong>and</strong> peanut intercropping<br />
(Photo: IDRC (www.idrc.ca), used with permission.)<br />
Plate 15. Morphological variability of leaves in Z. mauritiana<br />
146
Plates 16 & 17. Flowering <strong>and</strong> fruit set in<br />
Z. mauritiana<br />
147
Plate 18. cv. Ponda<br />
Plate 19. cv. Illaoichi<br />
148
Plate 20. cv. Umran<br />
Plate 21. cv. Kaithli<br />
149
Plate 22. cv. Banarsi Kadaka<br />
Plate 23. cv. Seb<br />
150
Plate 24. cv. Gola<br />
Plate 25. cv. Katha Phal<br />
151
Plate 26. Morphological variability of fruits in Z. mauritiana<br />
Plate 27. Morphological variability of stones in Z. mauritiana<br />
152
10.1 Introduction<br />
Chapter 10. Marketing<br />
S. Azam-Ali<br />
The following in<strong>for</strong>mation on ber is mostly that given by Pareek (2001). In<br />
India, ber fruits are marketed though a marketing channel that differs according<br />
to <strong>the</strong> quality of produce, distance from <strong>the</strong> market <strong>and</strong> available storage <strong>and</strong><br />
marketing infrastructure.<br />
O<strong>the</strong>r producing countries in Asia (e.g. Afghanistan, Bangladesh, Myanmar,<br />
China) produce fruit largely <strong>for</strong> <strong>the</strong> local rural people <strong>and</strong> local markets.<br />
Thail<strong>and</strong> contrasts with <strong>the</strong>se countries because enhanced production has been<br />
geared to potential exports.<br />
Chinese jujube is becoming more intensively grown in China, especially in<br />
st<strong>and</strong>ardised agro<strong>for</strong>estry systems, <strong>and</strong> its production is increasing in Vietnam<br />
<strong>and</strong> Azerbaijan. Government policies provide <strong>for</strong> production <strong>for</strong> known local<br />
dem<strong>and</strong>s <strong>and</strong> China national markets are targets as well as exports.<br />
However in many cases, practices relate to growth of jujubes on a number of<br />
marginal l<strong>and</strong>s since trees are considered to be extremely hardy. The major<br />
cultivated species also produce naturalised populations in many areas of Africa<br />
<strong>and</strong> Asia; providing local produce <strong>and</strong> <strong>the</strong> fruits are relatively unimproved.<br />
10.2 <strong>Ber</strong><br />
Verma <strong>and</strong> Gujar (1994) outlined six main marketing channels which operate<br />
in Rajasthan in India. These are:<br />
1. Producer-Retailer 1 -Consumer<br />
2. Producer-Commission agent 2 -Retailer-Consumer<br />
3. Producer-Wholesaler 3 -Retailer-Consumer<br />
1 Retailer purchases fruits in <strong>the</strong> market from producers or pre-harvest<br />
contractors through <strong>the</strong> commission agent, or from a wholesaler, <strong>and</strong> sells <strong>the</strong>m<br />
in <strong>the</strong> local market or outside areas.<br />
2 Commission agent is a licence holder middleman trader with a permanent<br />
shop in <strong>the</strong> market. He sells on a commission basis. This is fixed by <strong>the</strong> market<br />
committee on <strong>the</strong> basis of <strong>the</strong> value of <strong>the</strong> produce.<br />
154
4. Producer-Commission agent-Wholesaler-Retailer-Consumer<br />
5. Producer-Pre-harvest contractor 4 -Commission agent-Retailer-Consumer<br />
6. Producer-Pre-harvest contractor-Commission agent-Wholesaler-<br />
Retailer-Consumer<br />
Marketing of ber fruits is also carried out through <strong>the</strong> following two channels:<br />
1. Producer-Commission agent-Wholesaler-Outside markets<br />
2. Producer-Pre-harvest contractor-Commission agent-Wholesaler-Outside<br />
markets.<br />
The farmer-seller brings <strong>the</strong> fruit to <strong>the</strong> market <strong>and</strong> pays charges <strong>for</strong><br />
transportation from <strong>the</strong> farm to <strong>the</strong> market, including loading <strong>and</strong> unloading<br />
costs. The buyer pays overhead charges such as market fee (1.6 % of <strong>the</strong> value<br />
of <strong>the</strong> produce), commission (4 % of <strong>the</strong> value of <strong>the</strong> produce) <strong>and</strong> weighing<br />
charges.<br />
In Chomu market in India, <strong>the</strong> producer, pre-harvest contractor, wholesaler <strong>and</strong><br />
retailer respectively, incurred 1.68-1.70 %, 5.80-6.62 %, 0.84-3.31 % <strong>and</strong> 0.07-<br />
6.92 % of <strong>the</strong> total marketing cost whereas <strong>the</strong> margins shared by <strong>the</strong>m were<br />
respectively 29.5-49.92 %, 7.36-8.35 %, 2.86-3.57 % <strong>and</strong> 41.14-48.31 %<br />
depending upon <strong>the</strong> marketing channel adopted (see Table 10.1). This reveals<br />
that <strong>the</strong> producer’s share of <strong>the</strong> consumer’s price is more than 46 % if sold<br />
directly in <strong>the</strong> market. But in that case, <strong>the</strong> producer would incur <strong>the</strong> cost of<br />
overseeing <strong>the</strong> fruit development period <strong>and</strong> <strong>the</strong> cost of harvesting, packing,<br />
transport to market <strong>and</strong> <strong>the</strong> work involved in dealing with <strong>the</strong> market<br />
functionaries. Thus, <strong>the</strong> highest share that could be obtained is nearly 33 %<br />
though pre-harvest contracts, which is ra<strong>the</strong>r low.<br />
3 Wholesaler is a licence holder in <strong>the</strong> market network who purchases fruits in<br />
bulk from farmers <strong>and</strong> <strong>o<strong>the</strong>r</strong> market functionaries <strong>and</strong> sells <strong>the</strong>m in <strong>the</strong> market<br />
at a higher price.<br />
4 Pre-harvest contractor takes out a contract <strong>for</strong> <strong>the</strong> orchard at <strong>the</strong> maturity<br />
stage (be<strong>for</strong>e harvest), fixing terms <strong>and</strong> conditions regarding <strong>the</strong> harvest with<br />
<strong>the</strong> farmer.<br />
155
Table 10.1 Percent price spread of ber in marketing through different<br />
channels in Chomu market (India) (from Pareek, 2001)<br />
Particulars<br />
Marketing channels<br />
1 2 3 4 5 6<br />
Producers net price 49.92 47.05 46.68 46.55 33.21 29.50<br />
Cost incurred by:<br />
Producer 1.70 1.70 1.68 1.68 - -<br />
Pre-harvest contractor - - - 6.62 5.80<br />
Wholesaler - - 0.84 3.31 - 2.83<br />
Retailer 0.07 6.92 4.11 3.98 6.95 3.71<br />
Total 1.77 8.62 6.63 8.97 13.57 12.34<br />
Margin of:<br />
Pre-harvest contractor - - - - 8.35 7.36<br />
Wholesaler - - 3.57 3.34 - 2.86<br />
Retailer 48.31 44.33 43.12 41.14 44.87 47.94<br />
Total 48.31 44.33 46.69 44.48 53.22 58.16<br />
A study of <strong>the</strong> marketing of ber in Chomu market in India is presented in table<br />
10.2. The table provides an analysis of <strong>the</strong> marketing costs of ber. The data in<br />
<strong>the</strong> table reveal that getting <strong>the</strong> produce into <strong>the</strong> market involves considerable<br />
ef<strong>for</strong>t <strong>and</strong> cost <strong>for</strong> transportation, packing <strong>and</strong> loading/unloading of <strong>the</strong><br />
produce. In addition, marketing of perishable produce is risk prone to spoilage.<br />
The harvesting season may coincide with <strong>o<strong>the</strong>r</strong> farm activities <strong>and</strong> <strong>the</strong> local<br />
market infrastructure may be inadequate <strong>and</strong> lack managerial assistance. The<br />
producer also has to deal with several market functionaries such as commission<br />
agents <strong>and</strong> wholesalers which is a cumbersome process <strong>and</strong> involves some<br />
uncertainties in <strong>the</strong> sale deeds. As a result, <strong>the</strong> producers often prefer to sell<br />
<strong>the</strong>ir produce by pre-harvest auction to contractors, just be<strong>for</strong>e fruit maturity.<br />
The contracts are fixed ei<strong>the</strong>r on <strong>the</strong> basis of a share of <strong>the</strong> income or on <strong>the</strong><br />
basis of a lump sum to be paid by <strong>the</strong> contractor in instalments. In <strong>the</strong> first case,<br />
<strong>the</strong> contractor takes care of overseeing <strong>the</strong> fruit development <strong>and</strong> picking <strong>and</strong><br />
grading, but <strong>the</strong> marketing is done jointly with <strong>the</strong> grower. In <strong>the</strong> second case,<br />
which is most common, <strong>the</strong> contractor picks <strong>the</strong> fruit according to his<br />
convenience <strong>and</strong> sells it in local or distant markets.<br />
156
Table 10.2 Components of cost (%) in marketing of ber through different channels at Chomu market in India<br />
(from Pareek, 2001)<br />
Particulars 1 2 3 4 5 6<br />
P* R** P R P W*** R P W R C R C W R<br />
Packing charges - - - - - - - - - - 30.59 - 29.48 - -<br />
Overseeing <strong>the</strong> - - - - - - - - - - 5.73 - 5.52 - -<br />
fruit development<br />
Transportation 35.87 - 7.36 7.81 9.45 - 12.78 6.99 6.04 9.64 4.64 6.39 4.47 3.13 6.25<br />
Packing 23.84 - 4.89 7.49 6.28 - 6.78 4.65 - 5.05 3.08 3.75 2.97 - 3.16<br />
Loading <strong>and</strong> 36.43 - 7.46 8.18 9.60 - 9.74 7.10 - 7.16 4.71 4.85 4.53 - 4.51<br />
unloading<br />
Loss due to - - - 24.33 - - 32.66 - - 22.50 - 15.87 - - 16.15<br />
damage<br />
Commission - - - 22.63 - - - - 21.51 - - 14.20 - 13.82 -<br />
Market fee - - - 9.06 - 11.69 - - 8.60 - - 5.69 - 5.53 -<br />
Weighing - 3.86 - 0.79 - 1.02 - - 0.76 - - 0.50 - 0.48 -<br />
Total 96.14 3.86 19.71 80.29 25.33 12.71 61.96 18.74 36.91 44.35 48.75 51.25 46.97 22.96 30.07<br />
* Producer; ** Retailer; *** Wholesaler; 1-6 See text<br />
157
In countries of sou<strong>the</strong>rn Africa where ber trees occur mostly as natural groves,<br />
small orchards, fences around fields or in homesteads, <strong>the</strong> fruits are sold after<br />
harvest ei<strong>the</strong>r in rural markets or are transported <strong>for</strong> sale in urban markets.<br />
There do not appear to be any defined marketing channels <strong>and</strong> transport is<br />
considered unreliable. Market studies in Malawi (Kaaria, 1998) in two urban<br />
markets (in Lilongwe <strong>and</strong> Limbe) <strong>and</strong> two rural markets (Salima <strong>and</strong> Monkey<br />
Bay) revealed <strong>the</strong> following:<br />
<br />
<br />
<br />
<br />
<br />
Distance from <strong>and</strong> access to <strong>the</strong> market determines who participates in<br />
<strong>the</strong> marketing of ber.<br />
Rural markets are mainly dominated by women while urban markets<br />
are dominated by male traders, who control <strong>the</strong> market <strong>and</strong> set <strong>the</strong><br />
prices.<br />
Marketing margins were higher in rural markets than in urban<br />
markets.<br />
Although <strong>the</strong> quantities of fruit sold <strong>and</strong> <strong>the</strong> prices have shown a<br />
steady increase, <strong>the</strong> markets will only grow if <strong>the</strong> governments initiate<br />
enabling policies that facilitate <strong>the</strong> development of rural-based<br />
marketing in<strong>for</strong>mation systems <strong>and</strong> build infrastructures that improve<br />
<strong>the</strong> transportation <strong>and</strong> market facilities.<br />
There is a need to develop mechanisms to st<strong>and</strong>ardise <strong>the</strong> packaging<br />
<strong>and</strong> added value.<br />
In Zimbabwe, ber fruits are ei<strong>the</strong>r sold in local markets (e.g. in Chikafa market)<br />
or in urban markets such as Harare, Mutare <strong>and</strong> Kadoma. Marketing is mainly<br />
done by women <strong>and</strong> youths, but occasionally men are involved (Kadzere,<br />
1998). Market studies on ber in Zimbabwe have revealed <strong>the</strong> following:<br />
<br />
<br />
<br />
<br />
<br />
The fruit production areas close to <strong>the</strong> Mozambique border are at<br />
some distance from <strong>the</strong> nearest market.<br />
Transport is unreliable.<br />
Formal markets do not exist <strong>and</strong> pricing is poor.<br />
There is a need <strong>for</strong> government policy <strong>for</strong> access to communal<br />
<strong>for</strong>estry resources, sale of traditional liquors in towns <strong>and</strong> levies etc.<br />
There is a need to develop a st<strong>and</strong>ard product <strong>for</strong> <strong>the</strong> market.<br />
Fruits are sold to bulk buyers in 20 litre tins containing between 15 <strong>and</strong> 20 kg<br />
of fruit at $5 to 20 per tin (Maposa <strong>and</strong> Chisuro, 1998). There is a barter system<br />
in place where fruits are exchanged <strong>for</strong> food items such as maize meal. This<br />
system is particularly active during food shortage years. A similar situation<br />
exists in Zambia (Kalikiti, 1998).<br />
<strong>Ber</strong> has remained almost unknown in <strong>the</strong> export market. The majority of fresh<br />
fruit is sold in local markets. However, <strong>the</strong>re is a growing dem<strong>and</strong> <strong>for</strong> <strong>the</strong> fruit<br />
outside of its place of growth. During <strong>the</strong> year 1995 to 1996, 645 MT of fresh<br />
158
er fruit were exported from India to countries such as South Africa,<br />
Bangladesh, Saudi Arabia, Bahrain <strong>and</strong> UAR.<br />
10.3 Chinese jujube<br />
Chinese jujube is produced mostly in quantity in countries with a centralised<br />
economy. In such countries, apart from satisfying <strong>the</strong> national requirements,<br />
some government attention is given to exports, <strong>and</strong> China exports to Thail<strong>and</strong><br />
in particular, after satisfying sustained dem<strong>and</strong> in regions such as Hong Kong<br />
<strong>and</strong> Taiwan. Both fruits <strong>and</strong> a powdered tea are promising products.<br />
Dehydrated fruits ‘Chinese Dates’ are exported from China (Kim et al., 1981);<br />
Yang <strong>and</strong> Niu, 1992) <strong>and</strong> <strong>the</strong> products are st<strong>and</strong>ardised. There is a clear growth<br />
potential here.<br />
10.4 Market prospects<br />
At present <strong>the</strong> markets <strong>for</strong> jujube fruits are mostly restricted to producing<br />
regions. The main reasons <strong>for</strong> this are:<br />
<br />
<br />
<br />
<br />
<br />
Most dem<strong>and</strong> being <strong>for</strong> fresh fruits ra<strong>the</strong>r than any processed<br />
products.<br />
Consumer interest somewhat limited due to a lack of awareness<br />
regarding <strong>the</strong> fruit, its nutritive value <strong>and</strong> its uses.<br />
Limited availability of fruits of an acceptable quality st<strong>and</strong>ard.<br />
Lack of st<strong>and</strong>ards <strong>for</strong> processed products.<br />
Lack of market in<strong>for</strong>mation systems <strong>and</strong> market infrastructure to meet<br />
<strong>the</strong> requirements of different stakeholders in local <strong>and</strong> export markets<br />
as well as processors.<br />
However, <strong>the</strong> dem<strong>and</strong> <strong>for</strong> <strong>the</strong> fruits is growing rapidly in inl<strong>and</strong> markets, but<br />
only slowly <strong>for</strong> export. Advertising through various media channels should<br />
fur<strong>the</strong>r increase consumer awareness <strong>and</strong> may lead to higher dem<strong>and</strong>s <strong>for</strong> <strong>the</strong><br />
fruit. Dem<strong>and</strong> <strong>for</strong> processed products can also be similarly created if <strong>the</strong><br />
st<strong>and</strong>ards of <strong>the</strong> products are improved <strong>and</strong> <strong>the</strong> quality maintained.<br />
159
Chapter 11. Current situation <strong>and</strong><br />
research needs<br />
J.T. Williams<br />
11.1 Summary of <strong>the</strong> current situation<br />
Both major jujubes are grown <strong>for</strong> <strong>the</strong>ir edible fruits which are high in vitamin<br />
C; fruits are eaten fresh, dried as dessert fruits, or c<strong>and</strong>ied <strong>and</strong> preserved in<br />
various ways. The Chinese jujube is a temperate tree growing in relatively dry<br />
areas <strong>and</strong> <strong>the</strong> Indian Jujube (ber) is grown in hot dry areas of <strong>the</strong> tropics <strong>and</strong> <strong>the</strong><br />
subtropics.<br />
Compared to <strong>o<strong>the</strong>r</strong> fruit trees, jujubes provide nutritious fruits at relatively low<br />
costs but <strong>the</strong>y remain under-utilised despite <strong>the</strong>ir multipurpose uses –<br />
whichever cultivated species is considered <strong>and</strong> wherever cultivated. In many<br />
areas fruits are still ga<strong>the</strong>red from wild st<strong>and</strong>s. Especially <strong>for</strong> Indian jujube<br />
(ber) <strong>and</strong> Chinese jujube a great deal of know-how exists on production<br />
techniques but many of <strong>the</strong>se have not been transferred through extension <strong>and</strong><br />
NGOs to poor farmers. There are vast regions of Asia <strong>and</strong> Africa where <strong>the</strong><br />
crops have been introduced <strong>and</strong> where transfer of existing technology would<br />
repay immediate dividends.<br />
Research <strong>and</strong> development studies on ber were limited until <strong>the</strong> 1960s to<br />
varietal trials <strong>and</strong> vegetative propagation studies in <strong>the</strong> States of Punjab <strong>and</strong><br />
Utter Pradesh in India. Since that time studies have exp<strong>and</strong>ed much more<br />
widely <strong>and</strong> addressed all aspects of ber cultivation, harvesting, grading,<br />
packaging <strong>and</strong> processing. Research in India has been paralleled by some<br />
research in Pakistan, Bangladesh <strong>and</strong> a number of countries in Africa.<br />
In India <strong>the</strong> past 40 years have witnessed very large increases in Z. mauritiana<br />
fruit production <strong>and</strong> much of this increase has been due to making ber<br />
profitable in ecologically poor, drought prone areas; <strong>the</strong>re is evidence of new<br />
larger-scale plantations being established in areas where <strong>o<strong>the</strong>r</strong> crops are not<br />
profitable.<br />
In China Chinese jujube, Z. jujuba has <strong>for</strong> <strong>the</strong> past 600 years traditionally been<br />
grown in an intercropping system <strong>and</strong> this accounts <strong>for</strong> 65 % of total supplies<br />
throughout China. In Hebei <strong>and</strong> Sh<strong>and</strong>ang provinces research attention has<br />
been given to <strong>the</strong> need <strong>for</strong> higher trunks be<strong>for</strong>e branching, crown densities, <strong>and</strong><br />
to plant spacing <strong>and</strong> orientation to maximise light penetration <strong>and</strong> duration. As<br />
a result wind speeds during <strong>the</strong> hot, dry wind season were greatly reduced to<br />
<strong>the</strong> benefit of intercrops (maize, cotton in <strong>the</strong> open parts <strong>and</strong> shade tolerant<br />
160
soybean, mung bean <strong>and</strong> <strong>o<strong>the</strong>r</strong>s nearer <strong>the</strong> trees) in summer. Wheat was most<br />
suitable in <strong>the</strong> winter when jujube trees are bare.<br />
Ziziphus mauritiana is also cultivated traditionally in Yunnan province of<br />
China where shifting cultivation was widely practised. In this region research<br />
attention has been given to more sustainable agrisilvicultural systems <strong>and</strong><br />
especially to insect pests which can become more of a problem when small<br />
orchards ra<strong>the</strong>r than scattered trees of ber are raised. Similar constraints<br />
relating to pests <strong>and</strong> diseases are likely to be apparent when an increase in<br />
jujube cultivation occurs in African countries <strong>and</strong> attention to <strong>the</strong>m will avoid<br />
economic losses.<br />
The major interests related to jujube production in whatever region or agroclimatic<br />
niche appear to be:<br />
1. Improving production <strong>and</strong> utilisation where <strong>the</strong> trees have long been<br />
cultivated so that enhanced production can be sustainable <strong>and</strong> economic.<br />
2. Improving socio-economic impacts by proving incomes <strong>for</strong> a range of<br />
off-farm activities related to marketing <strong>and</strong> processing.<br />
3. Developing management practices which are environmentally friendly<br />
<strong>and</strong> avoid large chemical inputs.<br />
4. Incorporating jujubes into l<strong>and</strong> systems aimed at helping<br />
environmental stability, in particular by incorporating jujubes into agro<strong>for</strong>estry<br />
systems, <strong>and</strong> as live fences.<br />
These interests will only be addressed by continued basic research to provide<br />
reliable planting materials of selected superior genotypes (especially with good<br />
fruit characteristics), protecting from major pests <strong>and</strong> diseases, <strong>and</strong> adaptation<br />
of genotypes to stress conditions.<br />
A range of applied research is also needed to adapt available agronomic<br />
techniques to planting systems <strong>for</strong> particular agroecological <strong>and</strong> climatic zones,<br />
to address processing techniques to prepare st<strong>and</strong>ard products from fruits, <strong>and</strong><br />
to underst<strong>and</strong> <strong>the</strong> socio-economic inputs <strong>and</strong> outputs over time – <strong>the</strong> results of<br />
which could justify credit systems to meet any recurrent high-cost farm<br />
operations.<br />
11.2 Need <strong>for</strong> in<strong>for</strong>mation dissemination<br />
ICUC issued its <strong>monograph</strong> on ber (Pareek, 2001) because <strong>the</strong>re was<br />
widespread need <strong>for</strong> in<strong>for</strong>mation prompted by a number of development<br />
initiatives, including provenance trials conducted in African countries under <strong>the</strong><br />
Semi Arid Lowl<strong>and</strong>s of West Africa programme of ICRAF. This had already<br />
linked to related activities in <strong>o<strong>the</strong>r</strong> parts of <strong>the</strong> continent e.g. in Botswana,<br />
Kenya, Malawi, Zimbabwe, Zambia <strong>and</strong> Lesotho.<br />
161
The <strong>monograph</strong> summarised important results of R & D in all parts of Asia <strong>and</strong><br />
Africa <strong>and</strong> much of <strong>the</strong> in<strong>for</strong>mation would not have been readily available<br />
<strong>o<strong>the</strong>r</strong>wise. This current <strong>monograph</strong> attempts to update <strong>the</strong> original compilation<br />
of in<strong>for</strong>mation so that it can be applied to any situation where any cultivated<br />
jujube will be <strong>the</strong> focus of interest.<br />
ICUC’s associated manual on ber (2002) was an essential adjunct <strong>for</strong> <strong>the</strong>se<br />
development initiatives involved with <strong>the</strong> transfer of technology.<br />
The attention of development initiates/organisations is drawn to <strong>the</strong> continued<br />
need to disseminate <strong>the</strong> results of ongoing research from one part of <strong>the</strong> world<br />
to an<strong>o<strong>the</strong>r</strong>.<br />
11.3 Research needs<br />
Whereas all aspects along <strong>the</strong> production to consumption chain require<br />
research, <strong>the</strong> following are most important.<br />
11.3.1 Underst<strong>and</strong>ing <strong>the</strong> genetic variation<br />
A modern assessment of <strong>the</strong> taxonomy of <strong>the</strong> genus Ziziphus is needed. The<br />
cultivated jujubes represent polyploid series <strong>and</strong> not enough is known about <strong>the</strong><br />
distribution of ploidy levels; <strong>the</strong>re are few, if any, voucher specimens with<br />
chromosome counts carried out <strong>and</strong> many taxa may be geographical variants or<br />
stabilised hybrids. Polyploid series exist within species <strong>and</strong> <strong>the</strong>re appears to be<br />
a range of self- <strong>and</strong> cross-incompatibilities in Ziziphus species, <strong>and</strong> although<br />
hybridisation has undoubtedly occurred it is hardly understood.<br />
Knowledge of <strong>the</strong> taxonomy would be rapidly enhanced by <strong>the</strong> wider use of<br />
molecular methods of analysis, not only in clarifying <strong>the</strong> status of taxa but in<br />
underst<strong>and</strong>ing <strong>the</strong> patterns of genetic diversity within wild <strong>and</strong> cultivated taxa.<br />
A genepool approach needs to be taken ra<strong>the</strong>r than one based solely on<br />
morphological types. Breeders simply do not know enough about those species<br />
which may have <strong>the</strong> required productivity, fruit quality or pest <strong>and</strong> disease<br />
resistance attributes which can be of great use in improvement programmes.<br />
Current cultivars are genetically hardly advanced from wild progenitors.<br />
Coupled with <strong>the</strong> need to underst<strong>and</strong> <strong>the</strong> genepool <strong>for</strong> targeted crop<br />
improvement is <strong>the</strong> need to identify taxa <strong>and</strong> a series of specific genotypes<br />
which can be of immediate value as rootstocks since jujubes will be more <strong>and</strong><br />
more propagated by grafting to perpetuate selected cultivar genotypes.<br />
In such research endeavours <strong>the</strong> limited research carried out to date using<br />
biochemical <strong>and</strong> molecular techniques should be exp<strong>and</strong>ed.<br />
162
Underst<strong>and</strong>ing <strong>the</strong> broader taxonomy of Ziziphus <strong>and</strong> <strong>the</strong> patterns of genetic<br />
variation in <strong>the</strong> cultivated species <strong>and</strong> <strong>the</strong>ir wild <strong>for</strong>ms can only emerge if<br />
concerted <strong>and</strong> well-planned research is initiated on an ecogeographical basis in<br />
parallel with assessment of ecotypic differentiation.<br />
For crops which are underutilised it cannot be expected that national<br />
programmes dealing with <strong>the</strong>m – <strong>and</strong> with minimal funding levels – can readily<br />
take on such wide-ranging research projects entailing geographical exploration,<br />
taxonomic <strong>and</strong> molecular analyses, grow-outs in several environments, testing<br />
as rootstocks <strong>and</strong> <strong>o<strong>the</strong>r</strong> related activities. Nor will such research necessarily be<br />
completed in a short time, e.g. that of a three-year project cycle, because <strong>the</strong><br />
materials may require several years of growth.<br />
There will be <strong>the</strong> need <strong>for</strong> national programmes to seek <strong>the</strong> cooperation of<br />
universities to work toge<strong>the</strong>r through strategic planning <strong>and</strong> joint research so<br />
that postgraduate research projects can be integral parts of <strong>the</strong> overall research<br />
programme. Additionally <strong>the</strong> value of networking across regions is clear to<br />
build a critical mass of researchers <strong>and</strong> to develop cooperative goals <strong>and</strong><br />
research. ICUC <strong>and</strong> UTFANET were responsible <strong>for</strong> recognition being<br />
accorded to jujubes as underutilised fruits <strong>and</strong> in <strong>the</strong> accelerated work on <strong>the</strong>m<br />
in <strong>the</strong> past few years. Such networking benefits <strong>the</strong> national programmes <strong>and</strong><br />
should be continued.<br />
On specific aspects of jujube variation, almost nothing is known about <strong>the</strong><br />
diversity in <strong>the</strong> primary centres of variation of <strong>the</strong> cultivated species <strong>and</strong> even<br />
less about any specific patterns of diversity that have emerged in secondary<br />
centres.<br />
11.3.2 Genetic improvement<br />
A large number of selections or cultivars is available <strong>for</strong> both Indian <strong>and</strong><br />
Chinese jujubes. These are named but <strong>the</strong>re is a great deal of confusion in <strong>the</strong><br />
naming. Better characterisation <strong>and</strong> perhaps molecular fingerprinting of<br />
accessions is needed in all existing germplasm collections. Additionally <strong>the</strong><br />
existing collections all appear to be inadequate <strong>and</strong> need expansion (see<br />
Chapter 9). Expansion is possible without <strong>the</strong> research proposed in 11.3.1<br />
above if related solely to cultivars, but <strong>the</strong>re is little point in adding to <strong>the</strong><br />
collections’ wild representatives of <strong>the</strong> cultivars until <strong>the</strong> variation patterns of<br />
<strong>the</strong> accessions are more fully understood. The objective has to be justifiable<br />
<strong>and</strong> meaningful germplasm collections to best serve improvement needs.<br />
Specific improvement objectives have been outlined in Chapter 8. However,<br />
<strong>the</strong>re is <strong>the</strong> need to carry out research through detailed genetic studies to<br />
underst<strong>and</strong> <strong>the</strong> heritability of quantitative <strong>and</strong> qualitative characters, especially<br />
those chosen as breeding targets. Selection is currently best served on very<br />
163
limited characters e.g. yield (kg/plant) or fruit attributes such as pulp/stone<br />
ratio.<br />
As jujubes become cultivated more <strong>and</strong> more in small- or medium-sized<br />
plantations <strong>the</strong>re is likely to be enhanced need to build into cultivars tolerances<br />
or resistances to pests <strong>and</strong> diseases; this requires continued research. The<br />
possibilities of polyclonal plantations to provide some insurance if <strong>the</strong>re are<br />
specific attacks is an area of research that has not been explored.<br />
Also as jujubes become cultivated more in marginal areas <strong>and</strong> on wastel<strong>and</strong>s<br />
<strong>the</strong>re will be <strong>the</strong> need to research satisfactory growth <strong>and</strong> fruit set under more<br />
extreme temperatures <strong>and</strong> to focus concerted breeding ef<strong>for</strong>ts to tailor cultivars<br />
to more diverse agroclimatic conditions. In this respect knowing more about<br />
<strong>the</strong> genetic relations between Z. mauritiana <strong>and</strong> Z. jujuba, <strong>and</strong> <strong>the</strong> possibilities<br />
of <strong>the</strong>ir crossing, would be helpful. Their climatic adaptations are different <strong>and</strong><br />
<strong>the</strong>ir vitamin C production differs but combining some attributes would be of<br />
interest <strong>and</strong> value, especially in new environments which currently result in<br />
poor production.<br />
Variation within cultivars exists <strong>for</strong> quality attributes although <strong>the</strong>y have been<br />
evaluated by multi-location testing so that <strong>the</strong>y can be recommended <strong>for</strong><br />
particular regions <strong>and</strong> conditions.<br />
Improvement is needed to incorporate resistances to major pests <strong>and</strong> diseases,<br />
adapt some cultivars to particular environmental stresses <strong>and</strong> to improve <strong>the</strong><br />
quality of fruits.<br />
When <strong>the</strong> research in 11.3.1 produces major results it can be used to assess <strong>the</strong><br />
existing germplasm collections to gauge how representative <strong>the</strong>y are in terms<br />
of covering <strong>the</strong> range of variation, what gaps exist which could usefully be<br />
filled in terms of materials readily available <strong>for</strong> genetic improvement <strong>and</strong><br />
genetic conservations, <strong>and</strong> <strong>the</strong>n progressively modify <strong>the</strong> collections. This also<br />
means that existing collections need fur<strong>the</strong>r research on characterisation.<br />
Due to <strong>the</strong> wide heterozygosity of natural populations it is important that any<br />
restructuring of germplasm collections does not result in <strong>the</strong>m becoming very<br />
large <strong>and</strong> costly to maintain. Linkages can be made with conservation<br />
organisations to maintain specific wild germplasm in situ when specific<br />
ecotypes or genotypes have been identified <strong>and</strong> characterised.<br />
The results of research on <strong>the</strong> taxonomy <strong>and</strong> analysis of patterns of variation<br />
will depend on exploration <strong>and</strong> sampling over large geographical regions <strong>and</strong><br />
also on assessing any ecogeographic difference. Strategic planning of <strong>the</strong><br />
research <strong>and</strong> funding <strong>for</strong> travel will be essential.<br />
164
11.3.3 Propagation<br />
It is likely that most jujubes used <strong>for</strong> enhanced production will be grafted.<br />
There is a need to develop rootstocks which can control <strong>the</strong> overall tree<br />
morphology <strong>and</strong> its vigour <strong>and</strong> to maximise its adaptation to different edaphic<br />
conditions. There is a need to st<strong>and</strong>ardise rootstocks in relation to productivity<br />
objectives, <strong>for</strong> use in orchard versus agro<strong>for</strong>estry systems because particular<br />
tree <strong>for</strong>ms (<strong>and</strong> vigour) are required <strong>and</strong> <strong>for</strong> use in adaptation to stress<br />
conditions. As pointed out in 11.3.2 <strong>the</strong>re is a need <strong>for</strong> basic research on<br />
rootstock genotypes <strong>and</strong> <strong>the</strong> ultimate goal should be to st<strong>and</strong>ardise a limited<br />
number of rootstocks which can be widely applied. Chapters 5 <strong>and</strong> 6 pointed to<br />
<strong>the</strong> value of mycorrhizae, <strong>and</strong> fur<strong>the</strong>r work on <strong>the</strong>se should be linked to <strong>the</strong><br />
selection of rootstocks.<br />
Knowledge derived from 11.3.1 above is basic in selecting <strong>the</strong> range of<br />
rootstocks <strong>and</strong> grafts to be attempted in order to lead to st<strong>and</strong>ard <strong>for</strong>ms.<br />
Fur<strong>the</strong>r research on rapid propagation using tissue culture <strong>and</strong> cuttings would<br />
be beneficial. The development of planting supply systems would benefit from<br />
accelerated research on cost-effective, replicable techniques of propagation,<br />
including micropropagation.<br />
11.3.4 Pruning/cropping systems<br />
Initial training of plants <strong>and</strong> subsequent pruning is needed. There is still scope<br />
to research pruning type <strong>and</strong> intensity in specific cultivars especially <strong>for</strong><br />
agro<strong>for</strong>estry situations which require a relatively open canopy.<br />
Reliable planting material of recommended cultivars needs to be accompanied<br />
by such in<strong>for</strong>mation, especially <strong>for</strong> situations where trees may be grown<br />
adjacent to houses, as windbreaks or in agro<strong>for</strong>estry systems all in <strong>the</strong> same<br />
area. A range of cultivars might be required to provide economic insurance to<br />
<strong>the</strong> growers. This is equally important as researching compatible intercrops.<br />
<strong>Jujubes</strong> are cultivated as scattered trees, in rainfed orchards or woodlots, in<br />
irrigated plantations <strong>and</strong> in rainfed <strong>and</strong> irrigated <strong>for</strong>estry systems. There is a<br />
need to research <strong>the</strong> optimal use of water <strong>and</strong> nutrients <strong>for</strong> sustained<br />
productivity of <strong>the</strong> jujubes <strong>and</strong>/or <strong>the</strong> cropping systems.<br />
Genotypes need to be selected <strong>for</strong> specific regimes of irrigation, rainfed<br />
systems <strong>and</strong> salinity <strong>and</strong> sodicity. This will require research on growth,<br />
assimilation rates <strong>and</strong> productivity <strong>and</strong> should be combined with l<strong>and</strong><br />
management to conserve water on wastel<strong>and</strong>s.<br />
165
11.3.5 Post-harvest studies<br />
Work on harvesting, grading <strong>and</strong> packaging of fruits has been undertaken <strong>and</strong> a<br />
number of recommendations exist. However, st<strong>and</strong>ard grading related to end<br />
use has hardly been implemented <strong>and</strong> more research is needed, not only on <strong>the</strong><br />
economics along <strong>the</strong> production to consumption chain but on <strong>the</strong> socioeconomic<br />
benefits particularly those affecting <strong>the</strong> well-being of family<br />
producers.<br />
Processing methods require st<strong>and</strong>ardisation with attention to cost-effectiveness<br />
<strong>and</strong> marketability of products from fruits. This requires additional research,<br />
especially if processing is to be at <strong>the</strong> community level. Incomes will be<br />
increased when processing methods to develop st<strong>and</strong>ard products acceptable in<br />
<strong>the</strong> markets are refined, st<strong>and</strong>ardised <strong>and</strong> downstreamed.<br />
In some cases suitable genotypes will need to be identified <strong>and</strong>/or selected <strong>for</strong><br />
specific processing needs.<br />
11.3.6 Marketing<br />
As with all underutilised crops attention has to be given to applied research<br />
such as storage, packaging <strong>and</strong> transportation of fruits <strong>and</strong> marketing. Since in<br />
many cases <strong>and</strong> many areas <strong>the</strong>re is limited availability of acceptable quality<br />
fruits <strong>and</strong> also lack of market in<strong>for</strong>mation systems, it is essential that<br />
researchers keep abreast of <strong>the</strong>ir development so that any interventions can be<br />
recommended.<br />
11.3.7 O<strong>the</strong>r relevant development issues<br />
Expansion of production, particularly at <strong>the</strong> local level, bears an initial<br />
establishment cost which at present is relatively high <strong>for</strong> clonal materials.<br />
Credit <strong>for</strong> such activities is often unavailable, as indeed it is <strong>for</strong> many aspects<br />
of rural development. NGOs should take seriously <strong>the</strong> need to set up<br />
cooperative credit mechanisms to assist in all aspects of production, processing<br />
<strong>and</strong> marketing, as well as to assist where infrastructure is not readily available<br />
<strong>for</strong> provision of inputs such as planting materials, chemicals <strong>and</strong> advice.<br />
166
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Journal of Mycology <strong>and</strong> Plant Pathology, 19(1): 105-106.<br />
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treatment with different chemicals <strong>and</strong> seed sizes on <strong>the</strong> germination behavior<br />
<strong>and</strong> seedling growth of ber (Ziziphus mauritiana Lam.). Environment <strong>and</strong><br />
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Singh, H. P. <strong>and</strong> Sindhu, S. S. (1985) Control of ber powdery mildew. Indian<br />
Horticulture, 29(4): 27.<br />
Singh, J. P. <strong>and</strong> Gupta, O. P. (1983) Evaluation of various packings of ber fruit<br />
in relation to decay loss caused by various microbes. Haryana Agricultural<br />
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Journal of Horticultural Science, 11: 5-12.<br />
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Progressive Horticulture, 17(1): 21-24.<br />
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19.<br />
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Singh, M. P. (1984 c) Studies on <strong>the</strong> activity of some insect pollinators of<br />
jujube (Ziziphus mauritiana Lamk.). Entomon, 9(3): 177-180.<br />
Singh, M. P. <strong>and</strong> Bal, J. S. (1986) Per<strong>for</strong>mance of Umran ber (Ziziphus<br />
mauritiana Lamk.) on different rootstocks. Horticultural Science, 21: 797.<br />
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Journal of Plant Protection, 12(1): 55-56.<br />
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Symposium, Horticultural Research-Challenging Scenario, Bangalore, India:<br />
39-40.<br />
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on vigour, yield <strong>and</strong> fruit quality of ber (Ziziphus mauritiana Lamk.) cv.<br />
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rootstocks. Journal of Research, Punjab Agricultural University, 25: 259-265.<br />
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<strong>and</strong> germination in Ziziphus. Plant Science, 11: 88-89.<br />
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Indian Journal of Agricultural Science, 44(6): 383-388.<br />
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in relation to <strong>the</strong> dormancy in jujube. Indian Journal Agricultural Science,<br />
44(10): 639-644.<br />
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(Ziziphus mauritiana Lamk.) under various storage conditions. National<br />
Symposium on Role of Food Technology in Rural Development, Haryana<br />
Agricultural University, Hisar, India.<br />
Singh, R. <strong>and</strong> Khanna, R. C. (1968) Some north Indian cultivars of ber. Indian<br />
Horticulture, 12(2): 23-26.<br />
Singh, R. <strong>and</strong> Tomar, N. S. (1988) Per<strong>for</strong>mance of some jujube (Ziziphus<br />
mauritiana) cultivars in semi-arid zone of Punjab. Indian Journal of<br />
Agricultural Science, 58(5): 382-383.<br />
Singh, R. R., Chauhan, K. S. <strong>and</strong> Singh, H. K. (1986) Effect of various doses of<br />
N, P <strong>and</strong> K on physico-chemical composition of ber fruit cultivar Gola.<br />
Progressive Horticulture, 18(1/2): 35-38.<br />
Singh, R. R., Jain, R. K. <strong>and</strong> Chauhan, K. S. (1983 a) Flowering <strong>and</strong> fruiting<br />
behaviour of ber (Ziziphus mauritiana Lamk.) under Gurgaon conditions.<br />
Haryana Agricultural University Journal of Research, 13(1): 112-114.<br />
Singh, R. S. (1997) Note on <strong>the</strong> effect of intercropping on growth <strong>and</strong> yield of<br />
ber (Ziziphus mauritiana Lamk.) in semi-arid regions. Current Agriculture,<br />
21(1/2): 117-118.<br />
Singh, R. S., Vashishtha, B. B. <strong>and</strong> Prasad, R. N. (1998) Micrometeorology of<br />
ber (Ziziphus mauritiana Lamk.) orchard grown under rainfed arid conditions.<br />
Indian Journal of Horticulture, 55(2): 97-107.<br />
Singh, R., Singh, P. <strong>and</strong> Bajwa, M. S. (1972 b) Effect of time of budding on its<br />
success in ber. Science <strong>and</strong> Culture, 38(4): 214-215.<br />
Singh, S. P. Fruit crops <strong>for</strong> wastel<strong>and</strong>. (1992) Fruit crops <strong>for</strong> wastel<strong>and</strong>.<br />
Scientific Publishers, Jodhpur, Rajasthan, India: 227.<br />
Singh, S. <strong>and</strong> Ahlawat, V. P. (1995) Physico-chemical attributes <strong>and</strong> mineral<br />
composition of ber leaves as affected by foliar application of urea <strong>and</strong> zinc<br />
sulphate. Haryana Journal of Horticultural Science, 24(2): 94-97.<br />
240
Singh, S. B., Chhabra, R. <strong>and</strong> Abrol, I. P. (1983 b) Effect of exchangeable<br />
sodium on <strong>the</strong> growth <strong>and</strong> mineral composition of jujube <strong>and</strong> guava. Indian<br />
Journal of Agricultural Science, 53(6): 446-450.<br />
Singh, S. B., Maheshwar, S. K. <strong>and</strong> Singh, P. N. (1995) Field evaluation of<br />
fungitoxicants against powdery mildew of ber (Ziziphus mauritiana Lamk.).<br />
Annals Plant Protection Sciences, 3(2): 168-169.<br />
Singh, S. P., Singh, I. B. <strong>and</strong> Singh, V. N. (1987 a) A note on effect of<br />
gibberellic acid on fruit setting, fruit retention <strong>and</strong> quality of jujube (Ziziphus<br />
mauritiana Lamk.) cv. Banarasi Karaka. Progressive Horticulture, 19(1-2): 61-<br />
64.<br />
Singh, S., Krishnamurthy, S. <strong>and</strong> Katyal, SL. (1967) Fruit Culture in India.<br />
ICAR, New Delhi, India.<br />
Singh, S., Singhrof, R. S. <strong>and</strong> Bhatia, S. K (2001) Effect of seed treatment on<br />
germination, growth, <strong>and</strong> budding success in ber root stock (Ziziphus<br />
rotundifolia) shown in nursery beds <strong>and</strong> poly<strong>the</strong>ne tubes. Haryana Journal of<br />
Horticultural Sciences, 30: 156-158.<br />
Singh, S., Singhrof, R.S. <strong>and</strong> Bhatia, S.K. (2001 a) Effect of transplanting<br />
treatment on success of ber (Zizyphus mauritiana Lamb). budding. Hayara<br />
Journal of Horticultural Sciences, 30: 159-160.<br />
Singh, U. P. <strong>and</strong> Singh, H. B. (1978) Occurrence of Fusarium demicellulare on<br />
living galls of Ziziphus mauritiana in India. Mycologia, 70(5): 1126-1129.<br />
Singh, U. R. <strong>and</strong> Singh, N. (1976) Effect of plant regulators on fruit drop, size<br />
<strong>and</strong> quality of ber (Ziziphus mauritiana Lamk.) var. Banarsi. Haryana Journal<br />
of Horticultural Science, 5: 1-8.<br />
Singh, U. R., P<strong>and</strong>ey, I. C., Tripathi, B. M. <strong>and</strong> Upadhyay, N. P. (1978 b)<br />
Effect of pruning on growth, yield <strong>and</strong> quality of ber (Ziziphus mauritiana<br />
Lamk.) cv. Karaka. Progressive Horticulture, 9(4): 12-16.<br />
Singh, U. R., Singh, D. V. <strong>and</strong> Singh, A. P. (1973 c) Study of some budded<br />
cultivars of ber (Ziziphus mauritiana Lamk.). Progressive Horticulture, 5(2):<br />
61-66.<br />
Singh, Z. <strong>and</strong> S<strong>and</strong>hu, A. S. (1984) Effect of pruning time on productivity <strong>and</strong><br />
physico-chemical characters of ber (Ziziphus mauritiana Lamk.) cv. Umran.<br />
Journal of Research, Punjab Agricultural University, 21(4): 521-524.<br />
241
Singh, Z. <strong>and</strong> S<strong>and</strong>hu, A. S. (1987) Effect of Atonik on physico-chemical<br />
characters of ber (Ziziphus mauritiana Lamk.) cv. Umran. Journal of Research,<br />
Punjab Agricultural University, 24(2): 240-242.<br />
Singh, Z., S<strong>and</strong>hu, A. S. <strong>and</strong> Dhillon, B. S. (1984 c) Studies on lopping <strong>and</strong><br />
topping in propagation of ber (Zizyphus mauritiana Lamk.). Punjab<br />
Horticultural Journal, 24(1): 60-62.<br />
Singh, Z., Dhillon, B. S. <strong>and</strong> S<strong>and</strong>hu, A. S. (1987 b) Chemical deblossoming<br />
<strong>and</strong> crop regulation in ber (Ziziphus mauritiana Lamk.) cv. Umran. Punjab<br />
Horticultural Journal, 27(1-2): 22-27.<br />
Singh, Z., Dhillon, B. S. <strong>and</strong> S<strong>and</strong>hu, A. S. (1991) Relationship of embryo<br />
degeneration with fruit drop <strong>and</strong> its pattern in different cultivars of ber. Indian<br />
Journal of Horticulture, 48(4): 247-251.<br />
Singhrot, R. S. <strong>and</strong> Kajal, R. S. (1986) Studies on <strong>the</strong> vegetative propagation of<br />
ber (Ziziphus mauritiana Lamk.). I. Effect of after budding treatments on <strong>the</strong><br />
budding success <strong>and</strong> budding growth. Haryana Journal of Horticultural<br />
Science, 15(3/4): 162-169.<br />
Singhrot, R. S. <strong>and</strong> Makhija, M. (1979 a) Vegetative propagation of ber<br />
(Ziziphus mauritiana Lamk.). II. The transplanting success of grafted ber plants<br />
at various stages of scion shoot growth. Haryana Journal of Horticultural<br />
Science, 8(1/2): 4-8.<br />
Singhrot, R. S. <strong>and</strong> Makhija, M. (1979 b) Vegetative propagation of ber<br />
(Ziziphus mauritiana Lamk.). III. Effect of time of sowing <strong>and</strong> acid treatment<br />
of ber seed germination <strong>and</strong> seedling per<strong>for</strong>mance. Haryana Journal of<br />
Horticultural Science, 8(3/4): 168-172.<br />
Singhrot, R. S., Bakhshi, J. C. <strong>and</strong> Singh, K. (1970) Vegetative propagation of<br />
ber (Ziziphus mauritiana Lamk.). I. Relative per<strong>for</strong>mance of seedlings raised in<br />
field <strong>and</strong> in alka<strong>the</strong>ne bags. Punjab Horticultural Journal, 10 (3/4): 181-186.<br />
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Appendix I Insect <strong>and</strong> mite pests of ber<br />
(Pareek 2001, updated).<br />
Order Scientific name Common<br />
name<br />
Author<br />
Diptera Carpomyia Fruitfly Basha, 1952;<br />
vesuviana<br />
Batra, 1953<br />
Dacus<br />
correctus,<br />
D. dorsalis<br />
Phyllodiplosis<br />
jujubae<br />
Lepidoptera Meridarchis<br />
scyrodes<br />
Meridarchis<br />
scyrodes<br />
Carposina<br />
niponensis<br />
Indarbela<br />
quadrinotata,<br />
I. watsoni,<br />
I. tetraonis<br />
Dasychira<br />
mendosa,<br />
Thiacidas<br />
postica<br />
Synclera<br />
univocalis<br />
Ancylis<br />
lutescens,<br />
Archips sp.<br />
Porthmolga<br />
paracina<br />
Tarucus<br />
balkanica,<br />
T. <strong>the</strong>ophrastus<br />
Pingasa<br />
dispensata<br />
Fruitfly Basha, 1952;<br />
Batra, 1953<br />
Occurrence<br />
India<br />
(Punjab,<br />
Aruppukottai,<br />
Jobner,<br />
Rahuri,<br />
S.K.Nagar)<br />
India<br />
(Jobner)<br />
Galls Gangwar, 1983 India<br />
(Allahabad)<br />
Fruit borer Sonawane <strong>and</strong> India<br />
Dorge, 1971 (Anantapur,<br />
Rahuri)<br />
Fruit borer Basha, 1952 India<br />
(Coimbatore)<br />
-- Huan et al. 1987 China<br />
Bark eating<br />
caterpillar<br />
Hairy<br />
caterpillar<br />
Leaf roller<br />
Leaf roller<br />
Leaf roller<br />
<strong>Ber</strong><br />
butterfly<br />
Semi<br />
looper<br />
Verma <strong>and</strong><br />
Singh, 1974;<br />
Mann <strong>and</strong><br />
Bindra, 1977<br />
Verma et al.,<br />
1972; Bhatnagar<br />
<strong>and</strong> Lakra, 1992,<br />
Kavitha <strong>and</strong><br />
Sovothri, 2001a<br />
Nayar et al.,<br />
1989<br />
Pareek <strong>and</strong><br />
Nath, 1996<br />
Chowdhury <strong>and</strong><br />
Majid, 1954<br />
Nayar et al.,<br />
1989<br />
Pareek <strong>and</strong><br />
Nath, 1996<br />
(Shanxi)<br />
India (Jobner,<br />
Rahuri, &<br />
S.K.Nagar)<br />
India (Jobner,<br />
Rahuri)<br />
India (Jobner,<br />
Rahuri)<br />
India<br />
(Rahuri)<br />
India<br />
India<br />
(Rahuri)<br />
India<br />
(Rahuri)<br />
258
Order Scientific name Common<br />
name<br />
Psorosticha Leaf<br />
(Tonica) zizyphi webber<br />
Coleoptera Holotrichia Cockchafer<br />
consanguinea beetle<br />
Aubeus sp.<br />
Grey<br />
weevil<br />
Author<br />
Verma, 1993<br />
Verma et al.,<br />
1972; Bhatnagar<br />
<strong>and</strong> Lakra, 1992<br />
Pareek <strong>and</strong><br />
Nath, 1996<br />
Occurrence<br />
India<br />
(Jodhpur)<br />
India<br />
(Jobner)<br />
India<br />
(Rahuri,<br />
Jobner)<br />
Myllocerus sp.<br />
Aubeus<br />
himalayanus<br />
Xanthochelus<br />
superciliosus<br />
Adoretus sp.<br />
Holotrichia<br />
serrata,<br />
Schizonycha sp.,<br />
Adoretus<br />
deccanus,<br />
A. kanarensis,<br />
A. stoliczkae<br />
Grey<br />
weevil<br />
Stone<br />
weevil<br />
Black<br />
weevil<br />
Cockchafer<br />
beetle<br />
Cockchafer<br />
beetle<br />
Wadhi <strong>and</strong><br />
Batra, 1964<br />
Pareek <strong>and</strong><br />
Nath, 1996;<br />
Gour <strong>and</strong><br />
Sriramulu, 1994<br />
Pareek <strong>and</strong><br />
Nath, 1996<br />
Trehan, 1956<br />
Pareek <strong>and</strong><br />
Nath, 1996<br />
Hemiptera Kerria lacca Lac insect Lakra <strong>and</strong> Kher,<br />
1990<br />
Parlatoria Scale insect Pareek <strong>and</strong><br />
zizyphus<br />
Nath, 1996<br />
Parlatoria Scale Gravena et al.,<br />
zizyphus<br />
1992<br />
Quadraspidiotus San Jose Ma et al., 1985<br />
perniciosus scale<br />
Drepanococus<br />
chiton<br />
Selenaspis<br />
articulatus<br />
Zyginida<br />
pakistanica<br />
Wax scale<br />
Scale<br />
Leaf<br />
hopper<br />
Mani <strong>and</strong><br />
Krishnamoorthy,<br />
1997<br />
Gravena et al.,<br />
1992<br />
Khangura <strong>and</strong><br />
S<strong>and</strong>hu, 1976,<br />
Kavitha <strong>and</strong><br />
Sovothri, 2001<br />
India<br />
India (Jobner,<br />
Rahuri,<br />
Hyderabad)<br />
India<br />
(Rahuri)<br />
India (Jobner,<br />
Rahuri)<br />
India<br />
India<br />
India<br />
(Jobner)<br />
Brazil<br />
China<br />
(Akesu,<br />
Xinjiang)<br />
India<br />
Brazil<br />
India<br />
(Punjab)<br />
India Anhdra<br />
Pradesh)<br />
259
Order Scientific name Common<br />
name<br />
Drosicha sp., Mealy bug<br />
Ferrisia<br />
consobrina,<br />
Nipaecoccus<br />
viridis<br />
Machaerota Spittle bug<br />
spangbergii,<br />
M. planitae<br />
Author<br />
Pareek <strong>and</strong><br />
Nath, 1996<br />
Pareek <strong>and</strong><br />
Nath, 1996;<br />
Nayar et al.,<br />
1989<br />
Nayar et al.,<br />
1989<br />
Nayar et al.,<br />
1989<br />
Pareek <strong>and</strong><br />
Nath, 1996<br />
Eurybrachys sp. Leaf<br />
hopper<br />
Agonoscelis Pantatomid<br />
nubila<br />
bugs<br />
Cadra calutella Pyralid<br />
moth<br />
Thysanoptera Thrips Yamdagni <strong>and</strong><br />
Gill, 1968<br />
Scirtothrips sp., Thrips Pareek <strong>and</strong><br />
Haplothrips sp.<br />
Nath, 1996<br />
Dolichothrips Leaf thrips Nayar et al.,<br />
indicus<br />
1989<br />
Scirtothrips Flower Nayar et al.,<br />
dorsalis thrips 1989<br />
Isoptera Odontotermes Termite Pareek <strong>and</strong><br />
sp.<br />
Nath, 1996<br />
Orthoptera Taeniopoda<br />
Rivera-Garcia,<br />
eques<br />
1988<br />
Acari<strong>for</strong>mes Eutetranychus Tetranychid<br />
orientalis mite<br />
Larvacarus<br />
transitans,<br />
Eriophyes<br />
cernus<br />
Gall mite<br />
Eriophid<br />
mite<br />
Kant <strong>and</strong> Arya,<br />
1969; T<strong>and</strong>on et<br />
al., 1976, Yadav<br />
et al. 2003<br />
Sharma, 1992<br />
Mukherjee et<br />
al., 1994<br />
Occurrence<br />
India<br />
(Rahuri)<br />
India<br />
India<br />
India (Jobner,<br />
Pusa-Bihar)<br />
India<br />
(Rahuri)<br />
India<br />
India<br />
(Jobner)<br />
India<br />
India<br />
India<br />
(Jobner)<br />
Mexico<br />
India<br />
(Jobner)<br />
India<br />
India<br />
260
Appendix II Ziziphus cultivars<br />
II.ia Ziziphus mauritiana cultivars in India (from Pareek, 2001)<br />
Ajmeri (Umran) (Gopani, 1976 a)<br />
Akhrota (Akrota) (Verma <strong>and</strong> Singh, 1974)<br />
Akola<br />
Aliganj (Chundawat <strong>and</strong> Srivastava, 1978)<br />
Babu (Gopani, 1976 a)<br />
Bachcha (Singh, 1969)<br />
Badami (Singh, 1969)<br />
Badshah Pas<strong>and</strong> (Singh et al., 1971, 1972a)<br />
Bagwadi (Pareek <strong>and</strong> Vashishtha, 1983, 1986)<br />
Bahadurgarhia (Dhingra et al., 1973)<br />
Banarsi (Banarasi) (Singh, 1969; Singh et al., 1971, 1972a)<br />
Banarsi Gola (Singh et al., 1973a)<br />
Banarsi Kadaka, (Banarsi Karaka, Karaka Varanasi, Kadaka, Karaka) (Singh et<br />
al., 1971, 1972a; Chundawat <strong>and</strong> Srivastava, 1978)<br />
Banarsi Peb<strong>and</strong>i (Singh et al., 1971, 1972a)<br />
Banarsi Pew<strong>and</strong>i<br />
Banarsi Prolific (Singh <strong>and</strong> Singh, 1973; Singh, 1964)<br />
Baruipur (Singh, 1964)<br />
Batasa<br />
Bawal Selection -2<br />
Bekata Varanasi (Ch<strong>and</strong>ra, 1964)<br />
Betawadi<br />
Betawadi Ha<strong>the</strong>d<br />
Bhavnagari<br />
BS- 1<br />
BS- 75-1<br />
BS- 75-2<br />
BS- 75-3<br />
Cantonment (Kundi et al., 1989 a)<br />
CAZRI Gola<br />
Chameli (Umran)<br />
Ch<strong>and</strong>ani Supari<br />
Chencho (Vashishtha <strong>and</strong> Pareek, 1989)<br />
Chhuhara (Singh et al., 1972a)<br />
Chhuhara Bawal<br />
Chonchal (Chundawat <strong>and</strong> Srivastava, 1978)<br />
D<strong>and</strong>an (R<strong>and</strong>hawa <strong>and</strong> Biswas, 1966)<br />
Dao Tien (Hoang <strong>and</strong> Tuynh, 1989)<br />
Darakhi-1<br />
Darakhi-2<br />
Deedwana (Vashishtha <strong>and</strong> Pareek, 1989)<br />
Desi Alwar (Alwar Desi) (Singh et al., 1971, 1972a)<br />
261
Dodhia (Chundawat <strong>and</strong> Srivastava, 1978)<br />
Foliso Alwari<br />
Ghughudanga (Singh, 1964)<br />
Gia Loc (Hoang <strong>and</strong> Tuynh, 1989)<br />
Glory (Glori) (Singh et al., 1971, 1972a)<br />
Gobindgarh Selection<br />
Gobindgarh Special (Verma <strong>and</strong> Singh, 1974)<br />
Godhan (Singh et al., 1973a)<br />
Gol (Singh, 1969)<br />
Gola Agra (Teaotia et al., 1974)<br />
Gola (Delhi Gola) (Singh <strong>and</strong> Khanna, 1968; Singh et al., 1973a)<br />
Gola Gurgaon-1 (a selection from Gola Gurgaon) (Dhingra et al., 1973)<br />
Gola Gurgaon-2 (a selection from Gola Gurgaon) (Verma <strong>and</strong> Singh, 1974)<br />
Gola Gurgaon-3 (a selection from Gola Gurgaon)<br />
Golan (Kundi et al., 1989 a)<br />
Golar (Singh et al., 1971, 1972a)<br />
Goli (R<strong>and</strong>hawa <strong>and</strong> Biswas, 1968)<br />
Golia<br />
Goma Kirti (Hiwale <strong>and</strong> Raturi, 1999)<br />
Gorifa<br />
Gorva (Singh et al., 1971, 1972a)<br />
Gularbasi (Singh <strong>and</strong> Khanna, 1968)<br />
Guli<br />
Harial<br />
Haq Nawaz (Kundi et al., 1989 a)<br />
Hoshiarpur<br />
Husain Riso Chinese<br />
Illaichi (Singh et al., 1971, 1972a)<br />
Illaichi Jhajjar (a selection of Illaichi)<br />
Jal<strong>and</strong>hari (Jullundhri) (Dhingra et al., 1973)<br />
Jeevan (Gopani, 1976 a)<br />
Jhajjar Selection<br />
Jhajjar Special<br />
Jogia (Singh et al., 1971, 1972a)<br />
JS II (Srivastava <strong>and</strong> Srivastava, 1978)<br />
Kabra (Singh et al., 1973a)<br />
Kadoda<br />
Kaithli (Kaithali) (Singh et al., 1971, 1972a)<br />
Kaki<br />
Kakrola Gola (Godara, 1981)<br />
Kala Gola (Singh et al., 1971, 1972a)<br />
Kali (Pareek <strong>and</strong> Vashishtha, 1983, 1986)<br />
Kalianwali<br />
Kaolang-1 (Chiou <strong>and</strong> Weng, 1996)<br />
Katha (Umran) (Pareek <strong>and</strong> Vashishtha, 1983, 1986)<br />
Katha (Umran) Bombay (Singh et al., 1971, 1972a)<br />
262
Katha (Umran) Gurgaon (Singh et al., 1971, 1972a)<br />
Katha (Umran) Rajasthan<br />
Kathaphal (Katha Phul) (Singh et al., 1971, 1972a; Chundawat <strong>and</strong> Srivastava,<br />
1978)<br />
Kharak, Kharki-2<br />
Kharki-1<br />
Khatti (Bisla et al., 1980)<br />
Kheera (Singh <strong>and</strong> Khanna, 1968)<br />
Khirni<br />
Kismish<br />
Laddu (Dhingra et al., 1973)<br />
Lakhan<br />
Lal Wali (Kundi et al., 1989 a)<br />
Lam (Vashishtha <strong>and</strong> Pareek, 1989)<br />
LR-9 (Kundi et al., 1989 a)<br />
LR-11 (Kundi et al., 1989 a)<br />
LR-13 (Kundi et al., 1989 a)<br />
Lucknow Karaka (Teaotia et al., 1974)<br />
Madhuri<br />
Maharwali (Vashishtha <strong>and</strong> Pareek, 1989)<br />
Ma Hong (Hoang <strong>and</strong> Tuynh, 1989)<br />
Manukhi<br />
Meharun<br />
Mirchia (Dhingra et al., 1973)<br />
MPKV<br />
Mundia (Mundia Murhera, Muria Mahrara) (Chundawat & Srivastava, 1978)<br />
Nagpuri (Singh, 1964)<br />
Nalagarhi<br />
Narikelee (Singh, 1964)<br />
Narikeli (Kasir-Bogri Kool Daccai Kool) (Dutta, 1954)<br />
Narma (Singh, 1969)<br />
Narma (Narma Varanasi)<br />
Nazuk<br />
Nehru M<strong>and</strong>al<br />
Nimaj<br />
Noki (Godara et al., 1980)<br />
Pameli<br />
Pathani<br />
Pew<strong>and</strong>i (Teaotia et al., 1974)<br />
Ponda<br />
Popular Gola<br />
Raja (Gopani, 1976 a)<br />
R<strong>and</strong>eri<br />
Reshmi (Godara et al., 1980)<br />
Rewa Selection (Godara et al., 1980)<br />
Rohtaki Gola<br />
263
Safarch<strong>and</strong>i (Padule et al., 1988)<br />
Safarch<strong>and</strong>i (Ha<strong>the</strong>d)<br />
Safeda (Sufeda) (Chadha et al., 1972)<br />
Safeda Rothak (Dhingra et al., 1973)<br />
Safeda-1 (a selection of Safeda)<br />
Sakhari (Ha<strong>the</strong>d)<br />
Sanaur-1 (Singh et al., 1973 a)<br />
Sanaur-2 (Singh et al., 1973 a)<br />
Sanaur-3<br />
Sanaur-4 (Tomar, 1986)<br />
Sanaur-5 (Khera <strong>and</strong> Singh, 1976)<br />
Sanaur-6 (Tomer, 1986)<br />
S<strong>and</strong>hura Narnaul (Chundawat <strong>and</strong> Srivastava, 1978)<br />
S<strong>and</strong>hura No-1<br />
Sasni Gola<br />
Seb<br />
Seedless<br />
Safeda Selected (Chundawat <strong>and</strong> Srivastava, 1978)<br />
Seo (Dhingra et al., 1973)<br />
Seo Bahadurgarhia (Godara et al., 1980)<br />
Shamber<br />
Shanba (Ha<strong>the</strong>d)<br />
Singhan<br />
Sua (Khra <strong>and</strong> Singh, 1976)<br />
Sua M<strong>and</strong>i<br />
Sukawani<br />
Supari<br />
Surati, Surti<br />
Surti Katha<br />
Talod Seedless<br />
Telong (Chiou <strong>and</strong> Weng, 1996)<br />
Tasbataso<br />
Thian Phien (Hoang <strong>and</strong> Tuynh, 1989)<br />
Thornless (Singh, 1964)<br />
Tikadi<br />
Triloki (Tiloki) (Singh, 1969)<br />
Umran (Katha) (Dhingra et al., 1973)<br />
Vikas (Chovatia et al., 1993)<br />
Vikas -2 (a selection of Vikas)<br />
Villaiti<br />
Wilayti (Walaiti) (Dhingra et al., 1973)<br />
ZG-1<br />
ZG-2 (Tomar, 1986)<br />
ZG-3 (Singh <strong>and</strong> Singh, 1973)<br />
Cultivar names in brackets are regional <strong>for</strong>ms of <strong>the</strong> same cultivar.<br />
264
Appendix II.ib Ziziphus mauritiana cultivars widespread in Assam<br />
Bali<br />
Deccaikool<br />
Kasir<br />
Kool<br />
Narkelle (Umran)<br />
Tenga Mitha<br />
Umran<br />
Appendix II.ic Ziziphus mauritiana cultivars popular in Pakistan<br />
Chamcal<br />
D<strong>and</strong>an<br />
Desi<br />
Karela<br />
Karnal<br />
Khathi Mithi<br />
Rohtak<br />
Saidork<br />
Sofeda Am<br />
Umran<br />
Appendix II.iia Ziziphus jujuba cultivars (from Pareek, 2001)<br />
Akhedi (Tagiev, 1976)<br />
Akhmedi (Tagiev, 1992)<br />
Arzu (Tagiev, 1976)<br />
Arzu (Tagiev, 1992)<br />
Bokjo (Park <strong>and</strong> Yu, 1989)<br />
Buluosa (Yu et al., 1991)<br />
Da-bai-tsao or Da-baj-czao (Sin’ko, 1977; Sivakov et al., 1988)<br />
Da-bal-tszao (Kucherova <strong>and</strong> Sin’ko, 1984a)<br />
Dongzao (Zeng, 1997)<br />
Druzhba (Sin’ko <strong>and</strong> Livinova, 1996)<br />
Gansu (Lu et al., 1993)<br />
Geumsung or Jh-12 (Yong et al., 1981)<br />
Hamazhao (Bi et al., 1990)<br />
Honey Jujube (Ming <strong>and</strong> Sun, 1986)<br />
Irada (Tagiev, 1976)<br />
Ja-2 (Kim <strong>and</strong> Kim, 1984 b)<br />
Ja-czao or Ya-tsao (Sivakov et al., 1988; Sin’ko, 1977)<br />
Jb- 21 (Kim <strong>and</strong> Kim, 1984 b)<br />
Jc-31 (Kim <strong>and</strong> Kim, 1984 b)<br />
265
Je-8 (Yong et al., 1981)<br />
Je-10 (Yong et al., 1981)<br />
Jg-10 (Kim <strong>and</strong> Kim, 1984 b)<br />
Ji-3 (Yong et al., 1981)<br />
Jianzhao (Bi et al., 1990)<br />
Jin Jujube (Ming <strong>and</strong> Sun, 1986)<br />
Jishen Hama Zao (Yu et al., 1991)<br />
Jixin Mi Jao (Yu et al., 1991)<br />
Jj-3 (Kim <strong>and</strong> Kim, 1984 b)<br />
Jk-4 (Kim <strong>and</strong> Kim, 1984 b)<br />
Khazari (Tagiev, 1976)<br />
Khurman (Akhundova <strong>and</strong> Agaev, 1989)<br />
Kitaiskii 60 (Sin’ko <strong>and</strong> Litvinova, 1996)<br />
Kitalskil 50 (Kucherova <strong>and</strong> Sin’ko, 1984 a)<br />
Kitalskil 52 (Romanova et al., 1985)<br />
Kitalskil 58 (Kucherova <strong>and</strong> Sin’ko, 1984 a)<br />
Kitalskil 86 (Romanova et al., 1985)<br />
Laohuyan (Liu <strong>and</strong> Wang, 1991)<br />
Lang (Lanham, 1926)<br />
Li (Lanham, 1926)<br />
Li Zao (Yu et al., 1991)<br />
Lingding Zao (Yu et al., 1991)<br />
Linze Small Jujube (Ming <strong>and</strong> Sun, 1986)<br />
Mardakyan (Tagiev, 1976)<br />
Mardakyanskil 6 (Kucherova <strong>and</strong> Sin’ko, 1984 a)<br />
Ming Shan Large Jujube (Ming <strong>and</strong> Sun, 1986)<br />
Moodeung or Ja-5 (Yong et al., 1981)<br />
Mu Shing Hong (Lanham, 1926)<br />
Nasimi (Tagiev, 1976)<br />
No. 1, 2, <strong>and</strong> 16/5 (Baratov et al., 1975)<br />
Ordubadi (Tagiev, 1992)<br />
Sanjo<br />
Sihong Dazao (Wan, 1994)<br />
Sovetskij (Sin’ko <strong>and</strong> Litvinova, 1996)<br />
Suantszao (Sin’ko <strong>and</strong> Litvinova, 1996)<br />
Sui-Men (Lanham, 1926)<br />
Taiso (Nikaido et al., 1990)<br />
Ta-jan-czao or Ta-yan-tsao or Ta-yan-tszao (Sivakov et al., 1988)<br />
Tan-yan-tszao (Rathore, 1986; Goncharova et al., 1990)<br />
Tavrika (Sin’ko <strong>and</strong> Litvinova, 1996)<br />
Tyantszao (Sin’ko <strong>and</strong> Litvinova, 1996)<br />
Ulduz (Tagiev, 1992)<br />
Vakhsh (Sin’ko et al., 1987)<br />
Vakhshskil 30/16 (Kucherova <strong>and</strong> Sin’ko, 1984 a)<br />
Vakhshskil 40/5 (Kucherova <strong>and</strong> Sin’ko, 1984 a)<br />
Vakhshskil 41-19 (Romanova et al., 1985)<br />
266
Vakhshskil 46/17 (Kucherova <strong>and</strong> Sin’ko, 1984 a)<br />
Wolchul Daechu (Kim et al., 1988)<br />
Ya-tszav (Romanova et al., 1985)<br />
Yan-jhao (Rathore, 1986)<br />
Yan-yan-tsao (Sin’ko, 1977)<br />
Yougji Hama Zao (Yu et al., 1991)<br />
Yubilenyl (Romanova et al., 1985)<br />
Ziangfen Hulu Zao (Yu et al., 1991)<br />
Appendix II.iib Ziziphus jujuba cultivars in <strong>the</strong> USA<br />
(from http://doityourself.com/fruits/givejujubeatry.htm <strong>and</strong> Outlaw, 2002)<br />
GA 866<br />
Li (Swoboda, Geant, Leen Burk)<br />
Lang<br />
Sherwood<br />
Silverhill (Tiger Tooth)<br />
So<br />
Sui Men (Shui Men)<br />
Sherwood is a columnar tree; So is a dwarf bush; <strong>o<strong>the</strong>r</strong>s are mostly small trees.<br />
267
Appendix III Research organisations<br />
working on jujubes<br />
Ziziphus mauritiana (ber)<br />
India: Organisations involved in ber research are as follows:<br />
The Indian Council of Agricultural Research (ICAR) initiated research on ber<br />
as a multi-location project in 1976 <strong>and</strong> later in 1978 as an All India Coordinated<br />
Research Project at <strong>the</strong> following ten centres:<br />
Department of Horticulture, CCS Haryana Agricultural University,<br />
Hisar - 124 004, India (N.R. Godara, S. Siddiqui, C. Gupta, R. K. Lakra,<br />
A. K. Gupta, P. K. Mehta, S. S. Dahiya).<br />
Dryl<strong>and</strong> Agriculture Research Station, CCS Haryana Agricultural<br />
University, Bawal, Haryana, India (R.A. Kaushik).<br />
Department of Horticulture, Rajasthan College of Agriculture,<br />
Rajasthan Agricultural University, Udaipur - 313 001, India.<br />
Department of Horticulture, SKN College of Agriculture, Rajasthan<br />
Agricultural University, Jobner - 303 329, India (N. L. Sen).<br />
Department of Horticulture, Mahatma Phule Agricultural University,<br />
Rahuri, Ahmednagar - 413 722, India (S. N. Kaulgud, K. N. Wavhal, D. P.<br />
Waskar).<br />
Dryl<strong>and</strong> Agriculture Research Station, Andhra Pradesh Agricultural<br />
University, Anantapur, India (K. S. Reddy).<br />
Division of Fruit <strong>Crops</strong>, Indian Institute of Horticultural Research,<br />
Hessarghatta Lake, Bangalore - 560 089, India (S. H. Jalikop, R. D.<br />
Rawal).<br />
Dryl<strong>and</strong> Agricultural Research Station, Tamilnadu Agricultural<br />
University, Aruppukottai, India (M. Selvarajan).<br />
Dryl<strong>and</strong> Agricultural Research Station, Gujarat Agricultural<br />
University, Sardarkrushinagar - 385 506, India (M. M. Patel).<br />
Department of Horticulture, Narendra Deo University of Agriculture<br />
<strong>and</strong> Technology, Kumarganj, Faizabad - 224 001, India (H. K. Singh).<br />
The following research institutes of <strong>the</strong> ICAR also conduct research<br />
programmes on ber:<br />
Central Institute <strong>for</strong> Arid Horticulture, Bikaner - 334 006, India (B. B.<br />
Vashishtha).<br />
Central Arid Zone Research Institute, Jodhpur - 342 003, India (R. N.<br />
Prasad, S. K. Lodha, K. D. Sharma, M. P. Singh).<br />
Central Horticulture Research Station, Indian Institute of Horticultural<br />
Research, Godhra - 389 001, Gujarat, India (S. S. Hiwale, B. G. Bagle).<br />
268
Division of Fruits <strong>and</strong> Horticultural Technology, Indian Agricultural<br />
Research Institute, New Delhi - 110 012 (V. P. Sharma, D. S. Khurdiya).<br />
Central Research Institute <strong>for</strong> Dryl<strong>and</strong> Agriculture, Hyderabad - 500<br />
059, India.<br />
<strong>Ber</strong> research was also initiated at several <strong>o<strong>the</strong>r</strong> Indian centres some of which<br />
are as follows:<br />
Regional Horticultural Research Station, Punjab Agricultural<br />
University, Bahadurgarh, Patiala, Punjab, India (H. Singh).<br />
Department of Horticulture, Punjab Agricultural University, Ludhiana<br />
- 141 004, Punjab, India (J. S. Bal, A. S. Dhatt, G. S. Bajwa, G. S. Mann).<br />
College of Agriculture, Gujarat Agricultural University, Junagadh,<br />
Gujarat, India (S. P. Singh).<br />
College of Agriculture, Gujarat Agricultural University, An<strong>and</strong> - 388<br />
001, Gujarat, India.<br />
Agriculture College <strong>and</strong> Research Institute, Tamilnadu Agricultural<br />
University, Madurai, Tamilnadu, India.<br />
University of Jodhpur, Jodhpur-342001, India (M. M. Bh<strong>and</strong>ari, N.<br />
Mathur, A. Vyas).<br />
Marathwada Agricultural University, Parbhani - 431401, India (V. K.<br />
Patil, S. D. Chavan).<br />
Department of Horticulture, CS Azad University of Agriculture <strong>and</strong><br />
Technology, Kanpur, India (A. Prasad, J. P. Shukla, U. R. Singh).<br />
Department of Horticulture, University of Agriculture <strong>and</strong><br />
Technology, Pantnagar, UP, India.<br />
Department of Horticulture, Faculty of Agriculture, Banaras Hindu<br />
University, Varanasi, India (C. B. Singh, S. P. Singh).<br />
O<strong>the</strong>r countries: Organisations involved in ber research in several <strong>o<strong>the</strong>r</strong><br />
countries are as follows:<br />
Pakistan Forest Research Institute, Peshawar, Pakistan (F. S. Khan).<br />
Dept. of Botany, University of Peshawar, Pakistan (F. Hussain).<br />
The Horticultural Research Institute, Department of Research &<br />
Specialist Services, PO Box 810, Marondera, Zimbabwe (N. Nenguwo).<br />
Department of Research & Specialist Services, Agronomy Institute,<br />
PO Box Cy 550, Causeway, Harare, Zimbabwe (I. Kadzere).<br />
Scientific <strong>and</strong> Industrial Research <strong>and</strong> Development Centre, PO Box<br />
6640, Harare, Zimbabwe (C. Mawadza, E. Chivero).<br />
Forestry Commission, PO Box 595, Highl<strong>and</strong>s, Harare, Zimbabwe (D.<br />
Rukuni).<br />
African Distillers, Box 2346, Harare, Zimbabwe (C. Guyo).<br />
International Centre <strong>for</strong> Research on Agro<strong>for</strong>estry, Bp 320, Samanko,<br />
Mali (M. Djimde).<br />
269
Institut D’Economie Rurale, BP 258, Bamako, Mali (M. Sidibe).<br />
ISRA/CIRAD- Foret Senegal, BP 2312, Dakar, Senegal (P. Danthu).<br />
Chercheur ISRA - Productions Forestieres Senegal, BP 2312, Dakar,<br />
Senegal (I. Diallo).<br />
Thusano Lefatsheng, P/Bag 00251, Gaborone, Botswana (T.<br />
Matlhare).<br />
Centre National de Semences Forestieres, 01 BP 2682 Ouagadougou,<br />
Burkina Faso (M. Ouedraogo).<br />
Kenya Forestry Research Institute, Social Forestry Programme, PO<br />
Box 0412, Nairobi, Kenya (B. Owuor Odit).<br />
Detache du CTFT-CIRAD Aupres de l’ICRAF, Nairobi, Kenya (D.<br />
Depommier).<br />
Forestry Research Institute of Malawi, Kufa Road, PO Box 270,<br />
Zomba, Malawi (L. Mwabumba).<br />
SADCC/ICRAF Agro<strong>for</strong>estry Project, PO BOX 134, Zomba, Malawi<br />
(H. Prins, J. A. Maghembe).<br />
Bunda College, University of Malawi, PO Box 219, Lilongwe,<br />
Malawi (M. Maliro).<br />
Agricultural Research Division, PO Box 829, Maseru 100, Lesotho<br />
(M. Mabusa).<br />
Ben Gurion University of <strong>the</strong> Negev, PO Box 653, Beer Sheva<br />
841051, Israel (A. Nerd, Y. Mizrahi).<br />
Tel Aviv University, Israel (Y. Waisel).<br />
Ziziphus jujuba (Chinese jujube)<br />
Research Centre of Chinese jujube, Hebei Agricultural University<br />
Baoding, Hebei 071001, China (M. J. Liu).<br />
Pharmaceutical Faculty, Beijing Medical University, Beijing 100083,<br />
China (C.Y. Cheng).<br />
Hebei Provincial Academy of Medical Sciences, Shijiazhuang<br />
050021, China (S. Wu, J. Zhang).<br />
Institute of Forest Science, Xingiang Vygur Autonomous Region,<br />
China (W. L. Ma).<br />
Station of Plant Protection <strong>and</strong> Quarantine, Jingyang County, Shanxi,<br />
China (J. L. Huan).<br />
Shanxi Agricultural University, Shanxi, China (K. Z. Li, Z. S. Gao).<br />
Department of Agriculture, Sou<strong>the</strong>ast Prefecture, Shanxi Province,<br />
China (Y. X. Wang).<br />
Institute of Forestry, Henan Academy of Agricultural Sciences,<br />
Zhenzhou, China (J. Z. Sun).<br />
Shangtung Academy of Agricultural Sciences, China (Z. Wang).<br />
Institute of Microbiology, Academia Sinicia, Peking, China (K. C.<br />
Mang).<br />
270
Research Institute of Economic Insects, CAF, Kunming 650 216,<br />
China (J. Li, X. Hu).<br />
Forestry Research Institute, Seoul 130 012, Republic of Korea (W. C.<br />
Bak).<br />
Department of Horticulture, Yeungnam University, Gyongsan 713-<br />
748, Republic of Korea (J. K. Byun, J. H. Do, K. H. Cheng).<br />
Naju Pear Research Institute, Fruit Tree Research Institute, R.D.A.,<br />
Naju 523-820, Republic of Korea (M. S. Yun, Y. S. Kim, C. S. Ahn).<br />
Department of Forestry, Kon-Kuk University, Seoul 133-701,<br />
Republic of Korea (G. C. Choo).<br />
Tokyo University of Agriculture, Japan (S. Nakayama).<br />
Apsheronskaya Opythaya, Stantsiva Subtropicheskikh Kul’tur, Baku,<br />
Azerbaijan (T. M. Tagiev).<br />
Samark<strong>and</strong>skil Filial NPO 703000 Samark<strong>and</strong>, Uzbekistan (G. M.<br />
Semenov).<br />
O<strong>the</strong>r Ziziphus species<br />
Laboratoire de Botanique Fundamental et Appliqué, Faculté des<br />
Sciences, Campus Universitaire, 1060 Tunis, Tunisia (M. B. Nasri-<br />
Ayachi).<br />
Botany Department, Faculty of Science, Mansoura University, Egypt<br />
(M. A. El-Demardesh).<br />
Botany Department, Faculty of Science, University of Cairo, Giza,<br />
Egypt (M. A. El-Demardesh).<br />
Botany Department, Faculty of Science, Assiut University, Assiut,<br />
Egypt (Z. A. R. El-Karemy).<br />
Institut Nationale de la Recherche Agronomique, BP 589, Seltat,<br />
Morocco (A. Tanji, F. Nassif).<br />
King Faisal University, Biology Department, Box 1759, Al-Hofuf<br />
31982, Saudi Arabia (K. H. Shaltout).<br />
Laboratorios de Botanica Lorenzo R. Parodi, Facultad de Agronomia<br />
de la Universidad de Buenos Aires, Avda. San Martin 4453. RA-1417,<br />
Buenos Aires, Argentina (G. M. Tourn).<br />
Institut fur Spezielle Botanik des Museums fur Naturkunde der<br />
Humboldt-Universitat zu <strong>Ber</strong>lin, Spathstrasse 80/81, <strong>Ber</strong>lin 1195,<br />
Germany (C. Schirarend).<br />
Institut Angew<strong>and</strong>te Botanik, University Muenster, Hindenburgplatz<br />
55, D-48143, Muenster, Germany (M. Popp, D. J. Von-Willert).<br />
Université Aix-Marseille III, URA CNRS 1152, Case 461, Saint<br />
Jerome, F-1 3397 Marseille/Cedex 20, France (P. Quezel).<br />
University Research International, Ef<strong>for</strong>d, Lymington SO41 0LZ, UK<br />
(S. C. Clif<strong>for</strong>d).<br />
Horticulture Research International, Wellesbourne, Warwick, CV35<br />
9EF, UK (H. G. Jones).<br />
271
Institute of Plant Physiology, University of Vienna, Vienna, Austria<br />
(K. Stefan).<br />
TAES, Research <strong>and</strong> Extension Centre, 17360 Coit Road, Dallas, TX<br />
78252-6582, USA (N. Sankhala).<br />
Fruit <strong>Crops</strong> Department, University of Florida, Gainesville, Florida<br />
32611, USA (P. M. Lyrene).<br />
Cali<strong>for</strong>nia University, Davis, Cali<strong>for</strong>nia, USA (A. A. Kader, A.<br />
Chordas).<br />
College of Agriculture, Basrah University, Basra, Iraq (M. F. Abbas,<br />
J. H. Al-Niami).<br />
272
Appendix IV List of jujube specialists<br />
1. Dr. Bal, J. S.<br />
Department of Horticulture<br />
Punjab Agricultural University<br />
Ludhiana - 141004, India.<br />
2. Dr. Batra, R. C.<br />
Department of Horticulture<br />
Punjab Agricultural University<br />
Ludhiana - 141004, India.<br />
3. Dr. Bhargava, B. S.<br />
Division of Soil Science<br />
Indian Institute of Horticulture<br />
Hassarghatta Lake<br />
Bangalore - 560 089, India<br />
4. Dr. Gupta, O.P.<br />
H.No. R25, Raghunagar, Pankha Road<br />
PALAM, New Delhi -110 058, India<br />
5. Dr. Gupta, O. P.<br />
Department of Plant Pathology<br />
CCS Haryana Agricultural University<br />
Hisar -125 004, India<br />
6. Dr. Khurdiya, D. S.<br />
Division of Fruits & Horticulture Technology<br />
Indian Agriculture Research Institute<br />
New Delhi -110 012, India.<br />
7. Dr. Lakra, R. K.<br />
Department of Entomology<br />
CCS Haryana Agricultural University<br />
Hisar -125 004, India.<br />
8. Dr. Pareek, O. P.<br />
Central Institute <strong>for</strong> Arid Horticulture,<br />
Bikaner -334006, India.<br />
(Res.- A-239, Karninagar Lalgarh, Bikaner - 334001)<br />
9. Dr. Raturi, G. B.<br />
Central Institute <strong>for</strong> Arid Horticulture<br />
Bikaner -334 006, India<br />
273
10. Dr. Rawal, R. D.<br />
Division of Plant Pathology<br />
Indian Institute of Horticultural Research<br />
Hesarghatta Lake, Bangalore - 560 089, India.<br />
11. Dr. Reddy, Y. N.<br />
College of Agriculture<br />
N.G. Ranga Andhra Pradesh Agricultural University<br />
Rajendranagar, Hyderabad - 500030, India.<br />
12. Dr. Singh, I. S.<br />
Department of Horticulture<br />
N.D. University of Agricultural & Technology,<br />
Kumarganj, Faizabad - 224 001, India.<br />
13. Dr. Vashishtha, B. B.<br />
Central Institute <strong>for</strong> Arid Horticulture<br />
Bikaner - 334 006, India<br />
274
Appendix V Seed suppliers directory<br />
AUSTRALIA<br />
Harvest Seeds<br />
325 Mc Carrs Creek Road<br />
NSW 2084<br />
Australia<br />
Tel: (61-2) 94502699<br />
Fax: (61-2) 94502750<br />
Email: harvest@ozemail.com.au<br />
M.L. Farrar Pty. Limited<br />
PO Box 1046<br />
Bomaderry, NSW 2541<br />
Australia<br />
Tel: (61-44) 217966<br />
Fax: (61-44) 210051<br />
Telex: AA171133 FLAMY<br />
BURKINA FASO<br />
Centre National De Semences<br />
Forestieres C.N.S.F<br />
01 BP 2682<br />
Ouagadougou 01<br />
Burkina Faso<br />
Tel: (226) 35 80 13, 35 61 11<br />
Fax: (226) 35 61 10<br />
Email: cnsf@fasonet.bf<br />
Website:<br />
http://members.spree.com/business/<br />
cnsf_bf/<br />
FRANCE<br />
CIRAD-Forêt<br />
Laboratoire de graines,<br />
Campus International de<br />
Baillarguet, BP 5035,<br />
34032 Montpellier Cedex 01<br />
France<br />
Tel: (33-4) 67593751<br />
Fax: (33-4) 67593733<br />
Email: labograine@cirad.fr<br />
UNITED KINGDOM<br />
Royal Botanic Gardens Kew<br />
Seed Conservation Dept.,<br />
Wakehurst Place,<br />
Ardingly, West Sussex. RH17<br />
6TN.<br />
United Kingdom<br />
Tel: 01444 894123<br />
Fax: 01444 894069<br />
Email: Seedbank@rbgkew.org.uk<br />
Website:<br />
rbgkew.org.uk/seedbank/msb.html<br />
The Henry Doubleday Research<br />
Association<br />
Ryton on Dunsmore<br />
Coventry, CV8 3LG<br />
United Kingdom<br />
Tel: (44-1203) 308215<br />
Fax: (44-1203) 639229<br />
Email:<br />
eroycrof@hdra.demon.co.uk<br />
INDIA<br />
Bisht Enterprises<br />
19, 1st Floor, Devki Complex<br />
Moti Bazar,<br />
Dehra Dun-248001 (UP)<br />
India<br />
Tel: (91-135) 773014 (Res)<br />
Fax: (91-135) 773331<br />
Gautam Global<br />
34 Old Connought Place<br />
Dehra Dun-248001, UP<br />
India<br />
275
Tel: (91/135) 656222<br />
Fax: (91/135) 651108, 650944,<br />
652766<br />
Email: npsonudd@nde.vsnl.net.in<br />
Website:<br />
www.garhwalhimalayas.com/gauta<br />
mglobal<br />
Kumar International<br />
Ajitmal 206121<br />
Etawah (UP)<br />
India<br />
Tel: 05683 - 54221<br />
Fax: 091 - 5688 - 51036<br />
Cable: Kumar International<br />
Neelkan<strong>the</strong>shwar Agro-Seeds <strong>and</strong><br />
Plantations<br />
Commercial complex, ‘C’ Block -<br />
C-29/X3, Dilshad Garden,<br />
DELHI-110 095<br />
India<br />
Tel: 2274277, 2119790, 2119744<br />
Fax: (0091-11) 2112974<br />
Shivalik Seeds Corporation<br />
47 - P<strong>and</strong>itwari, P.O. Prem Nagar<br />
Dehra Dun - 248007, U.P.<br />
India<br />
Tel: 91-135 - 773348<br />
Fax: 91-135 - 773776<br />
Email: hil<strong>and</strong>er@vsnl.com<br />
Tosha Trading Company<br />
161, Indira Nagar Colony,<br />
PO - New Forest,<br />
Dehra Dun, 248006 , U.P.,<br />
India<br />
Tel: (91-135) 620984<br />
Fax: (91-135) 620196<br />
Tropical Nursery & Seeds<br />
P<strong>and</strong>itwari, Lane No. 9<br />
P.O. Prem Nagar Hehra Dun-248<br />
007 (U.P)<br />
India<br />
Tel: 0135 - 77 37 22<br />
Fax: 91 - 135 - 77 37 22<br />
Viyaj Seed Stores<br />
PO Ranjhawawala (Raipur)<br />
Dehra Dun-248008 (U.P.)<br />
India<br />
Fax: (91-135) 629944<br />
KENYA<br />
Floral Products Agencies<br />
Mbale Township, Makutano;<br />
Mbale-Magada Rd,<br />
PO Box 1402 Maragoli<br />
Kenya<br />
Tel: (254-0331) 51454, 51308<br />
Fax: (254-0331) 51217<br />
Email:<br />
fpagencies@kakamega.africaonlin<br />
e.com.<br />
Kenya Forestry Seed Centre<br />
PO Box 20412<br />
Nairobi<br />
Kenya<br />
Tel: (254-154) 32484, 32893<br />
Fax: (254-154) 32844<br />
MALAWI<br />
Forestry Research Institute of<br />
Malawi<br />
PO Box 270<br />
Zomba<br />
Malawi<br />
Tel: (265) 522866, 522548<br />
Fax: (265) 522782<br />
NIGER<br />
Centre des Semences Forestieres<br />
BP 578<br />
Niamey<br />
Niger<br />
Tel: (227) 723182, 733339<br />
276
Fax: (227) 732784<br />
NETHERLANDS<br />
Setropa Ltd.<br />
PO Box 203<br />
1400 AE Bussum<br />
Ne<strong>the</strong>rl<strong>and</strong>s<br />
Tel: (31-35) 5258754<br />
Fax: (31-35) 5265424<br />
Cable: SETROPA BUSSUM<br />
SENEGAL<br />
Project National de Semences<br />
Forestieres (PRONASEF)<br />
BP 3818<br />
Dakar<br />
Senegal<br />
Tel: 836/14/11<br />
Fax: 836/14/09<br />
Email: pronasef@ns.arc.sn<br />
SINGAPORE<br />
The Inl<strong>and</strong> & Foreign Trading Co<br />
(Pte) Ltd.<br />
Block 79A Indus Road #04-418<br />
Singapore 169589<br />
Singapore<br />
Tel: (65) 2722711 (3 lines)<br />
Fax: (65) 2716118<br />
Email: iftco@pacific.net.sg<br />
TANZANIA<br />
National Tree Seed Programme<br />
PO Box 373<br />
Morogoro<br />
Tanzania<br />
Tel: (255-56) 3192, 3903<br />
Fax: (255-56) 3275<br />
Email: ntsp@twiga.com<br />
Website:<br />
http://www.twiga.com/ntsp<br />
USA<br />
F. W. Schumacher Co., Inc.<br />
36 Spring Hill Rd. S<strong>and</strong>wich.<br />
MA 02563-1023<br />
United States of America<br />
Tel: (1-508) 8880659<br />
Fax: (1-508) 8330322<br />
Lawyer Nursery Inc.<br />
950 Highway<br />
200 West Plains, Montana 59859<br />
United States of America<br />
Tel: (1-406) 8263881<br />
Fax: (1-406) 8265700<br />
Telex: 406-31-9547<br />
Email: lawyrnsy@montana.com<br />
Source: Kindt et al. (2001)<br />
277
Glossary<br />
actinomorphic - having radially symmetric shape, usually refers to <strong>the</strong> petals of<br />
a flower.<br />
acuminate - <strong>the</strong> shape of a tip or base of a leaf or perianth segment where<br />
<strong>the</strong> part tapers gradually <strong>and</strong> usually in a concave manner.<br />
adnate - joined to or attached to.<br />
albumen - Starchy <strong>and</strong> <strong>o<strong>the</strong>r</strong> nutritive material in a seed, stored as<br />
endosperm inside <strong>the</strong> embryo sac, or as perisperm in <strong>the</strong><br />
surrounding nucellar cells; any deposit of nutritive material<br />
accompanying <strong>the</strong> embryo.<br />
anatropous - bent over through 180 degrees to lie alongside <strong>the</strong> stalk.<br />
<strong>and</strong>roecium - all <strong>the</strong> male reproductive organs of a flower; <strong>the</strong> stamens. cf.<br />
gynoecium.<br />
angiosperm - a plant producing seed enclosed in an ovary. A flowering<br />
plant.<br />
annual - a plant that completes its life cycle from germination to death<br />
within one year.<br />
anterior - front; on <strong>the</strong> front side; away from <strong>the</strong> axis.<br />
an<strong>the</strong>r - <strong>the</strong> pollen-bearing (terminal) part of <strong>the</strong> male organs (stamen),<br />
borne at <strong>the</strong> top of a stalk (filament).<br />
an<strong>the</strong>sis - flower bud opening; strictly, <strong>the</strong> time of expansion of a flower<br />
when pollination takes place, but often used to designate <strong>the</strong><br />
flowering period; <strong>the</strong> act of flower bud opening.<br />
antrorse - turning upward <strong>and</strong> <strong>for</strong>ward.<br />
apex - <strong>the</strong> tip of an organ, <strong>the</strong> growing point.<br />
apical - pertaining to <strong>the</strong> apex.<br />
apiculate - having a short point at <strong>the</strong> tip.<br />
arcuate - bow-shaped.<br />
aril (arillus) - a fleshy or sometimes hairy appendage or outer covering of a<br />
seed.<br />
arillate - provided with an aril.<br />
auricle (adj. auriculate) - small ear-like projections at <strong>the</strong> base of a leaf or leafblade<br />
or bract.<br />
axil - <strong>the</strong> upper angle <strong>for</strong>med by <strong>the</strong> union of a leaf with <strong>the</strong> stem.<br />
axillary - pertaining to <strong>the</strong> organs in <strong>the</strong> axil, e.g. buds, flowers or<br />
inflorescence.<br />
axis - <strong>the</strong> main or central stem of a herbaceous plant or of an<br />
inflorescence.<br />
basal - borne on or near <strong>the</strong> base.<br />
bifarous - in two rows; two-fold; pointing in two directions.<br />
bifid - <strong>for</strong>ked; having a deep fissure near <strong>the</strong> centre.<br />
bilabiate - two-lipped.<br />
bipinnate - (of leaves) a pinnate leaf with primary leaflets <strong>the</strong>mselves<br />
divided in a pinnate manner; cf pinnate.<br />
278
iseriate - in two rows.<br />
bisexual - having both sexes present <strong>and</strong> functional in one flower.<br />
blade - <strong>the</strong> flattened part of a leaf; <strong>the</strong> lamina.<br />
bract - a much-reduced leaf, particularly <strong>the</strong> small or scale-like leaves<br />
in a flower cluster or associated with <strong>the</strong> flowers;<br />
morphologically a foliar organ.<br />
bracteole - a secondary bract; a bractlet.<br />
caducous - falling off early, or prematurely, as <strong>the</strong> sepals in some plants.<br />
calyx - <strong>the</strong> outer whorl of floral envelopes, composed of <strong>the</strong> sepals.<br />
carinate - keeled; provided with a projecting central longitudinal line or<br />
ridge on <strong>the</strong> under surface.<br />
carpel - one of <strong>the</strong> flowers’ female reproductive organs, comprising an<br />
ovary <strong>and</strong> a stigma, <strong>and</strong> containing one or more ovules.<br />
clone - a group of plants that have arisen by vegetative reproduction<br />
from a single parent, <strong>and</strong> which <strong>the</strong>re<strong>for</strong>e all have identical<br />
genetic material.<br />
colpus (colpi pl.) - aperture within <strong>the</strong> pollen grain wall.<br />
concave - <strong>the</strong> interior of a curved surface.<br />
confluent - merging or blending toge<strong>the</strong>r.<br />
connate - united or joined; in particular, said of like or similar structures<br />
joined as one body or organ.<br />
convex - arched outward.<br />
cordate - heart-shaped, often restricted to <strong>the</strong> basal portion ra<strong>the</strong>r than to<br />
<strong>the</strong> outline of <strong>the</strong> entire organ.<br />
coriaceous - of lea<strong>the</strong>ry texture.<br />
cotyledon - seed leaf; <strong>the</strong> primary leaf or leaves in <strong>the</strong> embryo.<br />
crenate - shallowly round-too<strong>the</strong>d, scalloped.<br />
crenulate - finely crenate.<br />
cross pollination - <strong>the</strong> transfer of pollen from <strong>the</strong> an<strong>the</strong>r of <strong>the</strong> flower of one<br />
plant to <strong>the</strong> flowers of a different plant.<br />
crustaceous - of hard <strong>and</strong> brittle texture.<br />
cucullate - hooded; hood-shaped.<br />
cultivar - a race or variety of a plant that has been created or selected<br />
intentionally <strong>and</strong> maintained through cultivation.<br />
cuneate - wedge-shaped; triangular with <strong>the</strong> narrow end at point of<br />
attachment, as in <strong>the</strong> bases of leaves or petals.<br />
cuspidate - with an apex abruptly <strong>and</strong> sharply constricted into an<br />
elongated, sharp-pointed tip.<br />
cyme - a broad, more or less flat-topped, determinate flower cluster,<br />
with central flowers opening first.<br />
cymose - inflorescence showing <strong>the</strong> cyme arrangement.<br />
deciduous - falling at <strong>the</strong> end of one season of growth or life, as <strong>the</strong> leaves<br />
of non-evergreen trees.<br />
decoction - herbal preparation made by boiling a plant part in water.<br />
deflexed - bent abruptly downward; deflected.<br />
279
degree-day - a unit that represents one degree of difference from a given<br />
point (as 65°) in <strong>the</strong> mean daily outdoor temperature <strong>and</strong> that<br />
is used especially to measure heat requirements.<br />
dehiscence - <strong>the</strong> method or process of opening a seed pod or an<strong>the</strong>r.<br />
dentate - with sharp, spreading, course indentations or teeth,<br />
perpendicular to <strong>the</strong> margin.<br />
denticulate - minutely or finely dentate.<br />
derived - originating from an earlier <strong>for</strong>m or group.<br />
dichotomous - <strong>for</strong>ked, in one or two pairs.<br />
dicotyledon - a flowering plant with two cotyledons.<br />
dioecious - having male (staminate) <strong>and</strong> female (pistillate) flowers on<br />
different plants.<br />
diploid - having two sets of chromosomes.<br />
dipterous - having two wings.<br />
distichous - two-ranked, with leaves, leaflets or flowers on opposite sides<br />
of a stem <strong>and</strong> in <strong>the</strong> same plane.<br />
divaricate - spreading very far apart; extremely divergent.<br />
downy - covered with short <strong>and</strong> weak soft hairs.<br />
drupacious - a fruit showing <strong>the</strong> characteristics of a drupe.<br />
drupe - a fleshy one-seeded indehiscent fruit with seed enclosed in a<br />
stony endocarp; stone fruit.<br />
elliptic - oval in outline.<br />
emarginate - having a shallow notch at <strong>the</strong> extremity.<br />
endocarp - <strong>the</strong> inner layer of <strong>the</strong> pericarp or fruit wall.<br />
endosperm - <strong>the</strong> starch <strong>and</strong> oil-containing tissue of many seeds.<br />
entomophilous - insect pollinated.<br />
epigynous -<br />
borne on or arising from <strong>the</strong> ovary; used of floral parts when<br />
<strong>the</strong> ovary is inferior <strong>and</strong> flower not perigynous.<br />
exalbuminous - without albumen.<br />
exine - <strong>the</strong> outer coat of a pollen grain.<br />
exocarp - <strong>the</strong> outer layer of <strong>the</strong> pericarp or fruit wall.<br />
falcate - scy<strong>the</strong>-shaped; curved <strong>and</strong> flat, tapering gradually.<br />
fasicle - a condensed or close cluster.<br />
faveolate - honey-combed.<br />
ferrugineous - pertaining to or coloured like iron rust.<br />
filament - thread; particularly <strong>the</strong> stalk of <strong>the</strong> stamen, terminated by <strong>the</strong><br />
an<strong>the</strong>r.<br />
fili<strong>for</strong>m - thread-shaped, long, slender <strong>and</strong> terete.<br />
flexuose - zig-zag; bending from side to side; wavy.<br />
fulvous - dull, brownish-yellow.<br />
fuscous - dusky, greyish-brown.<br />
genus - a group of related species, <strong>the</strong> taxonomic category ranking<br />
above a species <strong>and</strong> below a family.<br />
genotype - <strong>the</strong> genetic constitution of an organism, acquired from its<br />
parents <strong>and</strong> available <strong>for</strong> transmission to its offspring.<br />
glabrous - not hairy.<br />
280
glaucous - bluish white; covered or whitened with a very fine, powdery<br />
substance.<br />
globose - globe-shaped.<br />
glabrescent - becoming glabrous with age.<br />
glomeruli<strong>for</strong>m - showing a compactly, clustered <strong>for</strong>m.<br />
gynoecium - all <strong>the</strong> female parts of a flower.<br />
hoary (pubescent) - greyish white with a fine, close pubescence.<br />
homonym - a scientific name given two or more times to plants of <strong>the</strong><br />
same taxonomic rank but which are quite distinct from each<br />
<strong>o<strong>the</strong>r</strong>.<br />
hymenopterous - having four membranous wings.<br />
hypocotyl - <strong>the</strong> axis of an embryo below <strong>the</strong> cotyledons which on seed<br />
germination develops into <strong>the</strong> radicle.<br />
indehiscent - not regularly opening, as a seed pod or an<strong>the</strong>r.<br />
indigenous - native <strong>and</strong> original to <strong>the</strong> region.<br />
inflorescence - <strong>the</strong> flowering part of a plant <strong>and</strong> especially <strong>the</strong> mode of its<br />
arrangement.<br />
integuments - an outer covering or coat.<br />
IU (international unit) - a unit used to measure <strong>the</strong> mass of certain vitamins <strong>and</strong><br />
drugs based on <strong>the</strong>ir expected effects. For each substance to<br />
which this unit applies, <strong>the</strong>re is an international agreement<br />
specifying <strong>the</strong> biological effect expected with a dose of 1 IU.<br />
O<strong>the</strong>r quantities of <strong>the</strong> substance are <strong>the</strong>n expressed as<br />
multiples of this st<strong>and</strong>ard. Examples: 1 IU represents 45.5<br />
micrograms of a st<strong>and</strong>ard preparation of insulin or 0.6<br />
microgram of a st<strong>and</strong>ard preparation of penicillin. Consumers<br />
most often see IUs on <strong>the</strong> labels of vitamin packages: <strong>the</strong><br />
equivalent of 1 IU is 0.3 microgram (0.0003 mg) <strong>for</strong> vitamin<br />
A, 50 micrograms (0.05 mg) <strong>for</strong> vitamin C, 25 nanograms<br />
(0.000 025 mg) <strong>for</strong> vitamin D, <strong>and</strong> milligram <strong>for</strong> vitamin E.<br />
lateral - side shoot, bud etc.<br />
lamellae - a thin, flat plate or laterally flattened ridge.<br />
lanceolate - shaped like a lance head, several times longer than wide,<br />
broadest above <strong>the</strong> base <strong>and</strong> narrowed toward <strong>the</strong> apex.<br />
lenticellate - having a body of cells as a pore, <strong>for</strong>med on <strong>the</strong> periderm of a<br />
stem, <strong>and</strong> appearing on <strong>the</strong> surface of <strong>the</strong> plant as a lensshaped<br />
spot.<br />
liane - various high-climbing woody plants, usually found in <strong>the</strong><br />
tropics.<br />
locular - having a cavity or chamber inside <strong>the</strong> ovary, an<strong>the</strong>r or fruit.<br />
membranous - thin in texture, soft <strong>and</strong> pliable.<br />
mesocarp - <strong>the</strong> fleshy middle portion of <strong>the</strong> wall of a succulent fruit<br />
between <strong>the</strong> skin <strong>and</strong> <strong>the</strong> stony layer.<br />
monophyletic - descended from a single ancestral line, see also: polyphyletic.<br />
mucronate - terminated abruptly by a distinct <strong>and</strong> obvious spur or spiny tip.<br />
281
naturalised - to cause a plant to become established <strong>and</strong> grow undisturbed<br />
as if native.<br />
nectar - sweet secretion of gl<strong>and</strong>s in many kinds of flower.<br />
necrotic - Death of cells or tissues through injury or disease.<br />
nectiferous - producing nectar.<br />
nervules - small/minute nerves or veins.<br />
nodose - knobbly, knotty.<br />
obconical - inversely conical, having <strong>the</strong> attachment at <strong>the</strong> apex.<br />
oblique - slanting, unequal sided.<br />
obovate - inverted ovate; egg-shaped, with <strong>the</strong> broadest part above.<br />
obtuse - blunt or rounded at <strong>the</strong> end.<br />
octaploid - having eight times <strong>the</strong> basic number of chromosomes.<br />
orbicular - circular.<br />
osseous - bony.<br />
ovary inferior - with <strong>the</strong> flower-parts growing from above <strong>the</strong> ovary.<br />
ovary superior - with <strong>the</strong> flower-parts growing from below <strong>the</strong> ovary.<br />
ovate - egg-shaped, with <strong>the</strong> broader end at <strong>the</strong> base.<br />
ovule - <strong>the</strong> body which after fertilisation becomes <strong>the</strong> seed.<br />
panicle - a loose irregularly compound inflorescence with pedicellate<br />
flowers.<br />
paniculate - borne in a panicle.<br />
papillose - bearing minute, nipple-shaped projections.<br />
paripinnate - a pinnate (compound) leaf with all leaflets in pairs.<br />
pedicel - a tiny stalk; <strong>the</strong> support of a single flower.<br />
pendulous - more or less hanging or declined.<br />
perianth - <strong>the</strong> floral envelope consisting of <strong>the</strong> calyx <strong>and</strong> corolla.<br />
pericycle - <strong>the</strong> tissue of <strong>the</strong> stele lying just inside <strong>the</strong> endodermis.<br />
perigynous - adnate to <strong>the</strong> perianth, <strong>and</strong> <strong>the</strong>re<strong>for</strong>e around <strong>the</strong> ovary <strong>and</strong> not<br />
at its base.<br />
petal - a division of <strong>the</strong> corolla; one of a circle of modified leaves<br />
immediately outside <strong>the</strong> reproductive organs, usually brightly<br />
coloured.<br />
petiole - <strong>the</strong> stalk of a leaf that attaches it to <strong>the</strong> stem.<br />
phenotype - <strong>the</strong> morphological, physiological, behavioural, <strong>and</strong> <strong>o<strong>the</strong>r</strong><br />
outwardly recognisable <strong>for</strong>ms of an organism that develop<br />
through <strong>the</strong> interaction of genes <strong>and</strong> environment.<br />
pilose - hairy, especially with soft hairs.<br />
pilosulous - minutely pilose.<br />
pinnate - a compound leaf consisting of several leaflets arranged on<br />
each side of a common petiole.<br />
polygamous - bearing male <strong>and</strong> female flowers on <strong>the</strong> same plant.<br />
polyphyletic - having members that originated, independently, from more<br />
than one evolutionary line.<br />
polyploidy - having more than two sets of chromosomes.<br />
polyporate - pollen grain with many apertures.<br />
282
porate (see tricolporate, polycolporate) - describes a pollen grain which has<br />
rounded apertures only.<br />
prolate - having flattened sides due to lengthwise elongation.<br />
propagate - to produce new plants, ei<strong>the</strong>r by vegetative means involving<br />
<strong>the</strong> rooting or grafting of pieces of a plant, or sexually by<br />
sowing seeds.<br />
prot<strong>and</strong>rous - refers to a flower, when <strong>the</strong> shedding of <strong>the</strong> pollen occurs<br />
be<strong>for</strong>e <strong>the</strong> stigma is receptive.<br />
protogynous - referring to a flower where <strong>the</strong> shedding of <strong>the</strong> pollen occurs<br />
after <strong>the</strong> stigma has ceased to be receptive.<br />
psilate - referring to a pollen grain having a smooth surface.<br />
pubescent - covered with hairs, especially short, soft <strong>and</strong> down-like.<br />
pulvinus - a swelling at <strong>the</strong> base of a leaf or leaflet.<br />
putamen - <strong>the</strong> shell of a nut, <strong>the</strong> bony part of a stone fruit.<br />
pyri<strong>for</strong>m - pear-shaped.<br />
raceme - a simple inflorescence of pediceled flowers upon a common<br />
more or less elongated axis.<br />
rachis - <strong>the</strong> main stalk of a flower cluster or <strong>the</strong> main leafstalk of a<br />
compound leaf.<br />
radicle - <strong>the</strong> portion of <strong>the</strong> embryo below <strong>the</strong> cotyledons that will <strong>for</strong>m<br />
<strong>the</strong> roots.<br />
ramification - branching<br />
reticulate - in <strong>the</strong> <strong>for</strong>m of a network, net veined.<br />
retuse - with a shallow notch at a rounded apex.<br />
rootstock - <strong>the</strong> root system <strong>and</strong> lower portion of a woody plant to which a<br />
graft of a more desirable plant is attached.<br />
rotundate - nearly circular; orbicular to oblong.<br />
rufous - reddish-brown.<br />
rugose - wrinkled.<br />
rugulose - covered with minute wrinkles.<br />
sc<strong>and</strong>ent - climbing but not self-supporting.<br />
scarify - to scar or nick <strong>the</strong> seed coat to enhance germination.<br />
sclerenchymatous - tissue composed of cells with thickened <strong>and</strong> hardened walls.<br />
scurfy - covered with tiny, broad scales.<br />
self pollination - <strong>the</strong> transfer of pollen from <strong>the</strong> an<strong>the</strong>r of a flower to <strong>the</strong> stigma<br />
of <strong>the</strong> same flower, or different flowers on <strong>the</strong> same plant.<br />
sepal - a division of a calyx; one of <strong>the</strong> outermost circle of modified<br />
leaves surrounding <strong>the</strong> reproductive organs of <strong>the</strong> flower.<br />
sericeous - bearing fine, usually straight, appressed hairs.<br />
serrate - having sharp teeth pointing <strong>for</strong>ward.<br />
serrulate - finely serrate.<br />
sessile - without a stalk.<br />
sheath - a tubular envelop.<br />
spathulate - gradually narrowing downward to a summit; spoon shaped.<br />
spinescent - 1. having spines, 2. terminating in a spine, 3. modified to <strong>for</strong>m<br />
a spine.<br />
283
stamen -<br />
staminode -<br />
stigma -<br />
stipule -<br />
strigose -<br />
style -<br />
subulate -<br />
sulcate -<br />
tetraploid -<br />
testa -<br />
thyrse -<br />
tomentose -<br />
tomentulose -<br />
tomentum -<br />
trabecular -<br />
transverse -<br />
tricolporate -<br />
trifid -<br />
tropism -<br />
truncate -<br />
tuberculate -<br />
unguiculate -<br />
valvate -<br />
virgate -<br />
zygomorphic -<br />
one of <strong>the</strong> male pollen-bearing organs of <strong>the</strong> flower.<br />
a sterile stamen, or any structure without an<strong>the</strong>r corresponding<br />
to a stamen.<br />
that part of a pistil through which fertilisation by <strong>the</strong> pollen is<br />
effected.<br />
an appendage at <strong>the</strong> base of a petiole, often appearing in pairs,<br />
one on each side, as in roses.<br />
beset with appressed, sharp <strong>and</strong> stiff hairs.<br />
<strong>the</strong> usually attenuated portion of <strong>the</strong> pistil connecting <strong>the</strong><br />
stigma <strong>and</strong> ovary.<br />
awl-shaped.<br />
grooved or furrowed.<br />
having four sets of chromosomes (twice <strong>the</strong> normal number of<br />
chromosomes).<br />
<strong>the</strong> outer seed coat.<br />
a contracted, cylindrical or ovoid <strong>and</strong> usually compact panicle.<br />
covered with a thick felt of radicles; densely pubescent with<br />
matted wool.<br />
ra<strong>the</strong>r tomentose.<br />
closely matted, woolly hairs.<br />
a transverse partition, complete or incomplete.<br />
cross-wise in position.<br />
having three apertures in <strong>the</strong> pollen grain wall.<br />
deeply divided or left in three parts.<br />
<strong>the</strong> movement of an organism in response to an external<br />
source of stimulus, usually toward or away from it.<br />
ending abruptly, as if cut off transversely.<br />
bearing tubercles, covered with warty lumps.<br />
narrowed, clawed.<br />
open by valves.<br />
w<strong>and</strong>-shaped; slender, straight <strong>and</strong> erect.<br />
capable of division by only one plane of symmetry.<br />
284
Index<br />
agro<strong>for</strong>estry, 18, 45, 77, 78, 154,<br />
161, 165<br />
cover crop, 78<br />
intercropping, 10, 58, 77, 146,<br />
160, 229<br />
agronomy<br />
in situ budding, 52, 118<br />
irrigation, 38, 44, 47, 51, 56, 59,<br />
60, 67, 165, 191, 198, 206,<br />
256<br />
mulching, 60<br />
nursery, 42, 44, 45, 46, 47, 51,<br />
52, 198, 203, 238, 241<br />
pruning, 31, 60, 63, 64, 65, 68,<br />
70, 72, 170, 171, 177, 184,<br />
185, 192, 194, 198, 208, 209,<br />
218, 219, 228, 229, 234, 238,<br />
241, 242, 245, 254<br />
rootstock, 10, 11, 48, 49, 50, 51,<br />
52, 94, 110, 165, 283<br />
spacing, 32, 45, 78, 160, 177<br />
transplanting, 10, 45, 46, 51, 53,<br />
55, 87, 175, 202, 208, 231,<br />
238, 241, 242<br />
air layering, 179<br />
altitudes, 10, 36<br />
amino acids, 19, 101, 172, 189<br />
Australia, 15, 37, 40, 41, 80, 171,<br />
187, 190, 251, 275<br />
Bahrain, 30, 159<br />
Bangladesh, 11, 13, 77, 110, 134,<br />
154, 159, 160, 168, 197, 198,<br />
201, 228, 231, 237<br />
biological control, 67<br />
breeding, 7, 80, 81, 84, 85, 88, 89,<br />
92, 102, 103, 104, 111, 163, 164,<br />
177, 211, 223, 243, 250<br />
budding, 48, 49, 51, 52, 201<br />
Burkina Faso, 41, 43, 46, 47, 176,<br />
183, 190, 191, 202, 220, 221,<br />
270, 275<br />
Cameroon, 41, 184, 220, 251<br />
carbohydrate, 19, 38, 70<br />
chemical control, 67, 191, 227,<br />
235, 250<br />
China, 5, 6, 10, 11, 13, 15, 16, 25,<br />
33, 34, 38, 58, 77, 80, 82, 84, 85,<br />
89, 93, 98, 100, 101, 111, 112,<br />
154, 159, 160, 161, 179, 180,<br />
196, 200, 210, 211, 212, 216,<br />
219, 227, 245, 252, 253, 255,<br />
256, 258, 259, 270, 271<br />
chromosome number, 85, 86, 177,<br />
184<br />
climate, 6, 31, 78, 99, 119, 234<br />
clonal selection, 196<br />
conservation, 3, 31, 32, 87, 108,<br />
110, 111, 112, 164, 210<br />
cost, 60, 99, 155, 156, 157, 161,<br />
165, 166<br />
cultivars, 8, 9, 11, 12, 16, 17, 19,<br />
37, 40, 44, 45, 48, 53, 54, 62, 67,<br />
68, 71, 72, 73, 74, 75, 79, 80, 81,<br />
82, 83, 84, 85, 86, 87, 89, 90, 91,<br />
92, 93, 94, 95, 96, 97, 98, 99,<br />
100, 101, 102, 103, 104, 105,<br />
106, 107, 108, 109, 110, 111,<br />
112, 113, 114, 117, 118, 119,<br />
126, 127, 130, 132, 138, 162,<br />
163, 164, 165, 168, 170, 171,<br />
172, 176, 181, 183, 184, 188,<br />
191, 192, 196, 197, 198, 199,<br />
200, 203, 204, 207, 208, 212,<br />
213, 217, 219, 220, 224, 225,<br />
227, 229, 235, 237, 239, 240,<br />
242, 245, 247, 249, 250, 251,<br />
255, 261, 265, 267<br />
cultivation, 5, 6, 15, 16, 47, 79, 82,<br />
97, 98, 99, 100, 110, 160, 161,<br />
171, 188, 189, 197, 199, 204,<br />
220, 228, 238, 279<br />
cuttings, 48, 54, 55, 91, 165, 195,<br />
199, 235, 246<br />
diseases<br />
285
Alternaria, 10, 72, 73, 75, 76,<br />
144, 145, 193, 211, 212, 229<br />
Colletotrichum gloeosporioides,<br />
75<br />
fruit rot, 75, 193, 219<br />
leaf spot, 72, 73, 74, 183, 193,<br />
199, 212, 223, 229, 231, 234,<br />
245, 250, 251<br />
mildew, 71, 191, 193, 199, 202,<br />
211, 222, 238, 241, 247, 254<br />
Oidium erysiphoides, 71, 80, 234<br />
Phoma hissarensis, 75<br />
Pleospora infectoria, 75, 212<br />
powdery mildew, 10, 71, 144<br />
rust, 10, 75, 145<br />
stem rot, 216<br />
Tricho<strong>the</strong>cium roseum, 75<br />
witches’ broom, 6, 75<br />
diversity, 3, 11, 16, 80, 92, 108,<br />
111, 112, 162, 163, 211<br />
drinks, 29, 226<br />
drought tolerance, 11, 38, 182<br />
ecology, 190<br />
Ethiopia, 9, 10, 12, 13, 178<br />
evaluation, 82, 83, 85, 100, 108,<br />
111, 140, 208, 229, 241, 243<br />
flower<br />
an<strong>the</strong>sis, 81, 96, 200, 278<br />
pollination, 167, 185, 200, 246,<br />
256, 257, 278, 279, 283<br />
fodder, 29, 30, 45, 93<br />
fruit<br />
development, 37, 97, 114, 155,<br />
156, 157<br />
drop, 59, 64, 66, 71, 72, 73, 81,<br />
86, 97, 102, 103, 104, 105,<br />
118, 120, 122, 170, 173, 179,<br />
185, 188, 190, 209, 220, 223,<br />
235, 241, 242, 246, 249, 255<br />
quality, 38, 44, 62, 63, 66, 80,<br />
82, 83, 84, 98, 119, 122, 162,<br />
170, 171, 173, 174, 185, 190,<br />
192, 194, 196, 198, 202, 203,<br />
209, 232, 239, 241, 245<br />
ripening, 76, 167, 169, 172, 173,<br />
175, 176, 178, 189, 207, 226,<br />
232, 237<br />
set, 10, 37, 61, 62, 63, 64, 71,<br />
80, 83, 86, 95, 96, 97, 102,<br />
103, 104, 105, 117, 118, 119,<br />
120, 164, 170, 173, 174, 185,<br />
209, 215, 220, 231, 232, 235,<br />
246, 249, 254, 255, 256, 282<br />
yield, 32, 59, 61, 62, 64, 65, 66,<br />
68, 70, 77, 99, 100, 102, 103,<br />
119, 171, 179, 181, 184, 192,<br />
194, 196, 198, 200, 207, 208,<br />
209, 218, 234, 239, 241, 247,<br />
255<br />
development, 37, 57, 59, 63, 70,<br />
71, 167, 168, 175, 191, 199, 200,<br />
205, 212, 215, 222, 234, 243,<br />
246, 250, 252, 253, 254, 256<br />
fungi, 26, 47, 63, 77, 121, 168,<br />
176, 194, 214, 227<br />
genetic resources, 92, 93, 110, 112,<br />
217, 223, 231<br />
germination, 41, 42, 43, 44, 46, 86,<br />
89, 95, 98, 99, 183, 205, 237,<br />
241<br />
germplasm collections, 9, 100, 103,<br />
109, 111, 163, 164<br />
grafting, 48, 49, 54, 55, 75, 91,<br />
162, 200, 205, 256, 283<br />
growth regulators, 43, 53, 63, 116,<br />
119, 120, 122, 124, 125, 173,<br />
178, 180, 188, 190, 199, 204,<br />
213, 216, 218, 233, 246, 249<br />
harvesting, 59, 61, 97, 113, 114,<br />
116, 117, 118, 119, 155, 156,<br />
160, 166<br />
ideotypes, 79<br />
improvement, 8, 9, 11, 16, 80, 81,<br />
82, 83, 85, 86, 92, 102, 103, 104,<br />
105, 108, 111, 162, 163, 164,<br />
201<br />
India, 1, 6, 10, 11, 12, 13, 14, 16,<br />
29, 31, 32, 33, 37, 38, 39, 41, 46,<br />
47, 50, 56, 57, 59, 60, 61, 62, 65,<br />
66, 67, 69, 70, 71, 72, 73, 77, 78,<br />
286
82, 83, 84, 87, 89, 94, 95, 96, 97,<br />
99, 100, 102, 103, 108, 109, 112,<br />
113, 114, 115, 117, 119, 122,<br />
126, 130, 138, 154, 155, 156,<br />
157, 159, 160, 169, 170, 174,<br />
175, 176, 177, 178, 179, 181,<br />
182, 183, 184, 185, 187, 188,<br />
189, 190, 192, 193, 194, 195,<br />
196, 200, 201, 202, 204, 208,<br />
209, 212, 213, 215, 216, 217,<br />
218, 219, 220, 221, 222, 223,<br />
224, 225, 226, 227, 228, 229,<br />
230, 232, 235, 236, 237, 238,<br />
239, 240, 241, 244, 245, 247,<br />
248, 249, 250, 251, 252, 253,<br />
254, 258, 259, 260, 261, 268,<br />
269, 273, 274, 275, 276<br />
Kenya, 9, 13, 41, 94, 161, 184, 197,<br />
199, 215, 231, 270, 276<br />
lac insect, 70, 259<br />
Lesotho, 161, 270<br />
Malawi, 13, 29, 158, 161, 201, 227,<br />
253, 270, 276<br />
manure, 47, 56<br />
marketing, 117, 154, 155, 156, 157,<br />
158, 161, 166<br />
medicinal, 35, 221, 223, 243<br />
medicines, 93, 140, 203, 206<br />
micropropagation, 165, 204<br />
minerals, 20, 118<br />
nutrition, 16, 18, 183, 191, 231<br />
nutritional composition, 114<br />
origin, 15, 85, 108, 112, 250, 257<br />
patch budding, 51, 197<br />
pests<br />
Adoretus decanus, 69<br />
A. kanarensis, 69, 259<br />
A. pallens, 69<br />
A. stoliezkae, 69<br />
A. versutus, 69<br />
bark eating caterpillar, 6, 68, 258<br />
Carpomyia vesuviana, 66, 80,<br />
84, 171, 174, 224, 225, 227,<br />
231, 239, 258<br />
chafer beetle, 69<br />
Dacus correctus, 66, 258<br />
D. dorsalis, 66, 258<br />
Dasychira mendosa, 68, 258<br />
Drepanococcus chiton, 70<br />
Droschiella tamarindus, 70<br />
Euproctis fraterna, 68, 176<br />
fruit borer, 67, 258<br />
fruitfly, 10, 66, 143, 258<br />
hairy caterpillars, 6, 68<br />
Indarbela quadrinotata, 68, 208,<br />
239, 250, 258<br />
I. tetraonis, 68, 258<br />
I. watsoni, 68, 258<br />
Kerria lacca, 32, 70, 209, 259<br />
leaf gall, 70<br />
leaf hopper, 70<br />
mealy bug, 70<br />
Meridarchis scyrodes, 67, 80,<br />
258<br />
mites, 70<br />
Phakospora ziziphi-vulgaris, 75<br />
Phyllodiplosis jujubae, 70, 188,<br />
258<br />
Scirtothrips dorsalis, 260<br />
Thiacidas postica, 68, 203, 213,<br />
258<br />
wax scale, 70<br />
weevil, 70<br />
Xanthochelus supercilosus, 70<br />
Zyginida pakistanica, 70, 259<br />
planting, 29, 31, 32, 45, 46, 51, 56,<br />
57, 58, 60, 77, 79, 118, 119, 161,<br />
165, 166, 198, 238, 247, 254<br />
pollination, 40, 79, 81, 84, 93, 96,<br />
211<br />
post harvest<br />
packaging, 51, 121, 122, 158,<br />
160, 166, 217, 219<br />
ripening, 42, 76, 97, 99, 100,<br />
101, 104, 113, 115, 116, 117,<br />
118, 120, 124, 125, 126, 139,<br />
140, 167, 168, 169, 172, 173,<br />
175, 176, 178, 189, 207, 226,<br />
232, 237<br />
shelf life, 80, 84, 89, 114, 115,<br />
121, 122, 123, 124, 125, 126,<br />
287
134, 192, 193, 207, 228, 231,<br />
236<br />
spoilage, 116, 121, 122, 123,<br />
127, 156, 201<br />
storage, 9, 41, 42, 80, 82, 89,<br />
100, 111, 112, 114, 116, 118,<br />
120, 121, 122, 123, 124, 125,<br />
126, 129, 134, 154, 166, 167,<br />
168, 169, 172, 174, 192, 193,<br />
195, 198, 199, 207, 217, 219,<br />
223, 226, 229, 230, 236, 240,<br />
246, 255<br />
processing, 181, 235<br />
dehydrated, 126, 127, 129<br />
drying, 37, 101, 127, 128, 129,<br />
204, 205, 207, 210, 255<br />
preserve, 107, 127, 130, 131,<br />
133, 135<br />
preserved, 132, 138, 139, 160<br />
pulp, 3, 5, 18, 19, 20, 30, 40, 66,<br />
67, 79, 80, 97, 98, 99, 100,<br />
101, 102, 103, 104, 105, 106,<br />
115, 116, 117, 120, 126, 127,<br />
134, 136, 137, 138, 139, 153,<br />
164, 189<br />
wine, 137, 201<br />
production, iii, 1, 15, 17, 20, 25,<br />
30, 32, 38, 39, 40, 42, 44, 45, 46,<br />
48, 65, 70, 83, 91, 112, 118, 119,<br />
135, 138, 154, 158, 160, 161,<br />
162, 164, 165, 166, 167, 190,<br />
201, 210, 214, 256<br />
cost, 77<br />
income, 77, 223<br />
properties, 4, 18, 20, 21, 22, 23, 25,<br />
28, 114, 132, 180, 188, 191, 213,<br />
253<br />
protein, 19, 20, 22, 30, 101<br />
pruning, 31, 49, 60, 63, 64, 65, 68,<br />
70, 71, 72, 104, 119, 122, 165,<br />
170, 171, 175, 177, 184, 185,<br />
192, 194, 198, 199, 208, 209,<br />
218, 219, 228, 229, 234, 238,<br />
241, 242, 245, 254<br />
rainfall, 5, 10, 36, 37, 38, 59, 65,<br />
71, 72, 234<br />
returns, 77, 99, 116<br />
Saudi Arabia, 10, 30, 34, 159, 168,<br />
186, 233, 271<br />
seed<br />
dispersal, 190<br />
germination, 39, 177, 178, 180,<br />
183, 184, 185, 189, 190, 191,<br />
196, 201, 202, 205, 206, 207,<br />
208, 213, 216, 218, 224, 226,<br />
234, 239, 242, 251, 255, 278,<br />
281, 283<br />
seed propagation<br />
germination, 39, 177, 178, 180,<br />
183, 184, 185, 189, 190, 191,<br />
196, 201, 202, 205, 206, 207,<br />
208, 213, 216, 218, 224, 226,<br />
234, 239, 242, 251, 255, 278,<br />
281, 283<br />
growth regulators, 173, 178, 180,<br />
190, 199, 204, 213, 216, 218,<br />
233, 246, 249<br />
rootstock seedlings, 48, 52<br />
selection, 79, 80, 81, 82, 85, 91,<br />
102, 103, 104, 105, 106, 108,<br />
165, 195, 196, 220, 255, 257,<br />
262, 264<br />
South Africa, 35, 159<br />
stem cuttings, 216<br />
stooling, 48, 55, 239<br />
sugars, 19, 20, 38, 63, 70, 100, 101,<br />
102, 117, 118, 120, 123, 125,<br />
140<br />
taxonomy, 3, 4, 162, 163, 164<br />
temperature, 36, 37, 43, 50, 54, 71,<br />
80, 83, 99, 111, 112, 118, 120,<br />
122, 123, 124, 125, 126, 131,<br />
133, 136, 137, 138, 139, 167,<br />
169, 199, 204, 223, 232, 251,<br />
280<br />
timber, 32, 45, 111<br />
top working, 188, 201<br />
training, 56, 57, 65, 165<br />
USA, 37, 210, 251, 272<br />
Uzbekistan, 168<br />
vernacular names, 12, 13<br />
viability, 41, 42, 50, 99, 111<br />
288
vitamins, 20, 281<br />
water management<br />
water harvesting, 59, 234<br />
weed control, 60, 171, 203<br />
wood, 29, 32, 50, 123, 194<br />
yield, 32, 60, 62, 64, 66, 79, 80, 82,<br />
83, 84, 96, 99, 102, 103, 104,<br />
105, 118, 119, 137, 164, 175,<br />
176, 185, 192, 208, 226, 240,<br />
247<br />
fruit, 32, 59, 61, 62, 64, 66, 70,<br />
77, 171, 179, 181, 184, 192,<br />
194, 196, 198, 200, 207, 208,<br />
209, 218, 234, 239, 241, 247<br />
Ziziphus jujuba, 36, 199<br />
Z. lotus, 4, 10<br />
Z. nummularia, 1, 10, 11, 15, 29,<br />
31, 33, 48, 87, 91, 93, 96, 110,<br />
111<br />
Z. oenoplia, 72<br />
Z. spina-christi, 4, 1, 6, 9, 10, 12,<br />
16, 29, 30, 34, 36, 48, 49, 54,<br />
110, 113, 139, 140, 169<br />
Z. xylopyra, 12<br />
Zambia, 14, 30, 158, 161, 202<br />
Zimbabwe, 12, 14, 29, 35, 38, 100,<br />
137, 158, 161, 181, 182, 187,<br />
201, 202, 213, 219, 220, 247,<br />
269<br />
289