Indian Journal of Plant Sciences ISSN: 2319-3824 (Online)
An Online International Journal Available at http://www.cibtech.org/jps.htm
2013 Vol. 2 (3) July-September, pp.35-42/Ghosh
Research Article
DIVERSITY AND DISTRIBUTION OF CLIMBING PLANTS IN
LITTORAL FOREST OF NORTH ANDAMAN NORTH ANDAMAN
ISLANDS, INDIA
*Asutosh Ghosh
Taxonomy and Biosystematics Lab, Department of Botany, University of Calcutta,
Kolkata, WB, India
*Author for Correspondence
ABSTRACT
The present study examined the floristic diversity, dominance, abundance and IVI of climbers and lianas
species in the tropical littoral vegetation of North Andaman forest. A total of 377 climbing plants
belonging to 53 species, 33 genera, and 20 families were identified. The most dominant families are
Papilionaceae (15.09%), Arecaceae (13.20%). These consisted of 27 liana and 26 herbaceous climber
species. Hook climbing was the most predominant (27%) climbing mechanism. The dominant species
recorded from this forest were Calamus andamanicus, (IVI-26.84), Daemonorops manii (IVI-16.73).
Tylophora indica shows the highest frequent (100%) species. Most of the species were randomly
distributed (60.37%) whereas some showed clumped distribution (39.62%).
Key Words: Diversity, Climbing Plants, Littoral, North Andaman
INTRODUCTION
Climbers occur in all woody ecosystem of the world although a high abundance is considered to be
characteristic of tropical and subtropical forests (Bongers et al., 2005). Specifically in tropical rain forest,
they comprise about 25-30% of species diversity (Schnitzer and Bongers, 2002). Climbers play important
ecological roles in the forest ecosystem dynamics and functioning (Nabe-Nielsen, 2001; Bongers et al.,
2002) they contribute substantially to canopy closure after tree fall and help stabilize the microclimate
underneath (Schnitzer and Bongers, 2002).
In spite of the numerous roles climbers play in ecosystems, little attention has been given to them they are
scanty treated in literature (Bongers et al., 2005) almost all work on forest plant communities have over
relied heavily on tree (Turner et al., 1996) probably due to commercial value of many trees among other
reasons (Bongers et al., 2005). A few quantitative ecological studies on lianas are available from the
forests of Sarawak (Proctor et al., 1983; Putz and Chai, 1987), Sabah, East Ma-laysia (Campbell and
Newbery, 1993), Queensland, Australia (Hegarty, 1989, 1990), Hunter Valley, New South Wales
(Chalmers and Turner, 1994), Knysna, South Africa (Balfour and Bond, 1993), Itu-ri, Congo (Makana et
al., 1998), Costa Rica (Lie-berman et al., 1996), Barro Colorado island, Pa-nama (Putz, 1984) and in the
subtropical humid forest of Bolivia (Pinard et al., 1999). Such studies are lacking from Indian forests,
except for the two recent works in the forest of Anamalais, Western Ghats (Muthuramkumar and
Parthasarathy, 2000; Srinivas and Parthasarathy, 2000) and from the Ka-lrayan hills, Eastern Ghats
(Kadavul and Partha-sarathy, 1999). North Andaman, a major group of islands, is rich in species
diversity. But very little information exists on the ecological aspects of the littoral forest communities
these Islands. The specific objectives of the present study was to determine the diversity and distribution
of climbing plants in the littoral forest of North Andaman as a way of contributing to the understanding of
the general floristic composition, abundance and diversity.
MATERIALS AND METHODS
The North Andaman is the northernmost island of the Andaman region and includes about 70 other
smaller islands. It is located between 1341 N to 1250 N latitudes and 9211 E to 9307 E longitudes,
covering an area of 1458 km2, and is separated from the Middle Andaman by Austin Strait.
35
Indian Journal of Plant Sciences ISSN: 2319-3824 (Online)
An Online International Journal Available at http://www.cibtech.org/jps.htm
2013 Vol. 2 (3) July-September, pp.35-42/Ghosh
Research Article
The phytosociological study in this region was carried out during the years 2001-2004, through nested
quadrate sampling method. Twelve quadrate plots (32 x 32 m) were studied for recording ground covers
(Mishra, 1966; Malhotra, 1973; Das and Lahiri, 1997; Rai et al., 2011) (Figure 1). In each quadrate the
climbing plants were enumerated and measured for girth (GBH >0.5 cm) at breast height. The collected
voucher specimens were processed into mounted herbarium sheets following the conventional
methodology (Jain and Rao, 1977) and were identified and deposited at CUH Herbarium.
Climbing mechanisms were also studied for each species and classified them based on observations in the
field and reliable references (Putz, 1984). The collected field-data were analyzed for Species structure
(frequency, density, abundance, basal area, importance value index (IVI), using the formula as suggested
by Mishra (1966), Phillips (1959), Das and Lahiri (1997) and Ghosh (2006). The species diversity was
determined using Shannon-Weiner’s Index (1963).
RESULTS AND DISCUSSION
In this Littoral forest, a total of 53 species of climbers and lianas were recorded, of which 52 species are
angiosperms, and one species is a Pteridophyte (Lygodium flexuosum). Within the angiosperms, 37
species are from the dicotyledons (24 genera, 15 families) and 15 species are from the monocotyledons (9
genera, 5 families). In such forest, 26 species (49.05%) are climbers and 27 species (50.94%) are lianas.
The most diverse families in terms of species richness were Papilionaceae (15.09%), Arecaceae (13.20%),
Caesalpiniaceae, Menispermaceae and Vitaceae (7.54%) (The details of the determined phytosociological
values are recorded in Table 1).
Within the 52 species, 20 species (37.73%) are hook climbers, 15 species (28.3%) are stem twiners, 9
(16.98%) tendril climbers, 5 (9.43%) root climbers, and 4 (7.54%) branch twiners (Figure 1).
It was found that Tylophora indica shows the highest frequency (100%) with density of 13.3333/hec. in
the forest; followed by Cissus discolor and Thunbergia laurifolia (frequency: 66.66%, density:
11.6667/hec). In four species (Species Codes: 6, 23, 25, and 32) the frequency is low (16.66%) with
density of 4.1666/hec.; followed by six species (Species Codes: 1, 9, 26, 27, 43 and 45) same frequency
(16.66%), but bit lower density (2.5/hec.).
It is found that Bridelia cinnamomea has highest relative abundance (8.2791) with 16.16% frequency in
the forest followed by Bridelia stipularis (rel. abund.- 3.9216, with frequency 16.16%); Calamus
longisetus (rel. abund.- 3.7764, with frequency 25%); Lygodium flexuosum (rel. abund.- 3.0502, with
frequency 16.16%); Tinospora cordifolia (rel. abund.- 2.9049, with frequency 25%) and Dalbergia
candenatensis (rel. abund.-2.7597, with 50% frequency). Among the littoral species, minimum rel.
abundance (0.8714) with 25% frequency has been found in two species Plecospermum andamanicum and
Scindapsus officinalis (Figure 2).
Data on density-Rank relationship of species show that Bridelia cinnamomea and Dalbergia volubilis
occupy first rank with maximum density 15.8333/hec, followed by Tylophora indica (13.3333/hec),
Cissus repens, Thunbergia laurifolia (11.6666/hec), Calamus longisetus (10.8333/hec), Capparis
floribunda, and Cissus discolor (10/hec) etc. The minimum density (1.6666/hec) is found in Diploclisia
glaucescens, Tetrastigma lanceolarium, Ventilago madraspatana etc. Except Bridelia cinnamomea, and
Dalbergia volubilis, other species show logarithmic pattern with regression value (R 2) =0.9843 (Figure 3).
From the plotting of mean and variance of species in the littoral forest it is evident that species having
values ranging from 0.1667-1.5833 and 0.3333-14.0833 of mean and variance respectively, whereas those
with the range from 0.0833-1.1667 and 0.0833-1.4773 of mean and variance respectively are generally
random in distribution in the habitat.
Degree of freedom is 11. The species are aggregated in distribution show 0 to 0.024371 probabilities with
chi square values ranging from 22 to 97.8421, whereas species of random distribution show probability of
0.027062 to 0.894982 with chi square values ranging from 5.6667 to 21.6667 (Figure 4).
Calamus andamanicus, shows the highest IVI (26.84), followed by Daemonorops manii (16.73),
Daemonorops kurzianus (16.42), Dalbergia candenatensis (13.35), Calamus longisetus (12.17), Tylophora
36
Indian Journal of Plant Sciences ISSN: 2319-3824 (Online)
An Online International Journal Available at http://www.cibtech.org/jps.htm
2013 Vol. 2 (3) July-September, pp.35-42/Ghosh
Research Article
indica (10.89). The minimum IVI (1.18) is found in Tetrastigma lanceolarium. Except Calamus
andamanicus, other species show logarithmic pattern with regression value (R 2) =0.9416 (Figure 5).
Types of climbers and lianas in Littoral forest.
Stem tw iner
20
Branch Tw iner
15
Tendril
No. of
climbers 10
& lianas.
Hook
5
Root climber
0
Figure 1: Types of climbers and lianas in Littoral forest
Rel. Abundance
Comparison of Relative Abundance and Frequency of
Species
y = 0.0571x + 0.1528
R2 = 0.8588
9
8
7
6
5
4
3
2
1
0
0
20
40
60
80
100
120
Frequency
Figure 2: Comparison of Relative Abundance and frequency of Littoral forest
Comparison of Density-Rank relation of Species
60
50
y = -25.77Ln(x) + 68.579
R2 = 0.9843
Rank
40
30
20
10
0
0
5
10
15
20
De ns ity/he c.
Figure 3: Comparison of density-rank relation of Littoral forest species
COMPARISON OF MEAN AND VARIANCE OF SPECIES IN
LITTORAL FOREST
16
14
VARIANCE
12
10
8
6
4
2
0
0
0.5
1
MEAN
1.5
Figure 4: Comparison of mean and variance of Littoral forest species
37
Indian Journal of Plant Sciences ISSN: 2319-3824 (Online)
An Online International Journal Available at http://www.cibtech.org/jps.htm
2013 Vol. 2 (3) July-September, pp.35-42/Ghosh
Research Article
Table 1: Phytosociological analysis of the recorded species [F= Frequency, D= Density, RA =
Relative Abundance, RD = Relative Density, RF = Relative Frequency, IVI = Importance Value
Index, A/F= Abundance and frequency Ratio]
Sp.
code
1
2
3
4
5
6
7
8
9
Species
Family
Adenia
cardiophylla
(Masters) Engler
Adenia trilobata (Roxb.)
Engl.
Ancistrocladus
tectorius
(Lour.) Merr.
Bridelia cinnamomea Hook.f
Bridelia stipularis (L.) Bl.
Passifloraceae
Caesalpinia
andamanica
(Prain) Hattink
Caesalpiniaceae
Caesalpinia bonduc
Roxb.
Caesalpinia crista L.
Caesalpiniaceae
(L.)
Ancistrocladacea
e
Euphorbiaceae
Euphorbiaceae
Caesalpiniaceae
Caesalpiniaceae
10
11
Calamus longisetus Griff.
Arecaceae
12
Calamus palustris Griff.
Arecaceae
13
14
Calamus pseudorivalis Becc.
Calamus viminalis Willd.
Arecaceae
Arecaceae
15
Capparis floribunda Wight
Cappariadaceae
16
Cayratia japonica (Thunb.)
Gagnep.
Cissus discolor Bl.
Vitaceae
Cissus repens Lam.
Vitaceae
Menispermaceae
18
19
20
21
22
Cyclea peltata (Lam.) Hook.
f. & Thomson
D
RA
RF
RD
Rel.
Dom.
IVI
A/F
Ratio
16.67
25
1.30
1.04
0.8
0.01
1.83
9
25
58.33
2.03
1.55
1.86
0.01
3.42
9.33
50
16.67
66.67
158.3
1.16
8.27
3.11
1.04
2.12
5.04
0.88
1.11
6.10
7.18
2.66
57
16.67
75
3.92
1.04
2.39
0.57
3.99
27
16.67
41.67
2.17
1.04
1.33
1.81
4.16
15
58.33
83.33
1.24
3.63
2.65
3.27
9.55
2.44
25
33.33
1.16
1.55
1.06
1.55
4.16
5.33
16.67
25
1.30
1.04
0.8
0.61
9
66.67
75
0.98
4.15
2.39
20.3
25
108.3
3.77
1.55
3.45
7.17
2.44
26.8
4
12.1
7
25
25
50
33.33
1.74
1.16
1.55
1.55
1.59
1.06
3.52
2.4
6.66
5.01
8
5.33
41.67
66.67
1.39
2.59
2.12
3.76
8.47
3.84
41.67
100
2.09
2.59
3.18
0.03
5.80
5.76
25
41.67
1.45
1.55
1.33
0.08
2.96
6.66
66.67
33.33
116.7
100
1.52
2.61
4.15
2.07
3.71
3.18
0.25
0.22
8.10
5.47
2.62
9
33.33
58.33
1.52
2.07
1.86
0.02
3.94
5.25
50
75
1.30
3.11
2.39
10.9
41.67
58.33
1.22
2.59
1.86
12.3
50
158.3
2.76
3.11
5.04
5.2
16.4
3
16.7
4
13.3
5
16.67
41.67
2.17
1.04
1.33
1.17
3.52
8
15
Passifloraceae
Caesalpinia
enneaphylla
Roxb.
Calamus andamanicus Kurz
17
F
Arecaceae
Vitaceae
Arecaceae
Daemonorops kurzianus
Becc
Daemonorops manii Becc
Arecaceae
1.68
17.33
3
3.36
Dalbergia
candenatensis
(Dennst.) Prain
Papilionaceae
Papilionaceae
24
Dalbergia
confertiflora
Benth.
Dalbergia junghuhnii Benth.
Papilionaceae
41.67
50
1.04
2.59
1.59
1.53
5.71
2.88
25
Dalbergia volubilis Roxb.
Papilionaceae
16.67
41.67
2.17
1.04
1.33
0.09
2.44
15
26
Derris andaminaca Prain
Papilionaceae
16.67
25
1.30
1.04
0.8
0.79
2.61
9
27
Derris elegans
andamanensis
16.67
25
1.30
1.04
0.8
1.03
2.86
9
23
Benth.
f.
6.33
Papilionaceae
38
Indian Journal of Plant Sciences ISSN: 2319-3824 (Online)
An Online International Journal Available at http://www.cibtech.org/jps.htm
2013 Vol. 2 (3) July-September, pp.35-42/Ghosh
Research Article
28
Dinochloa andamanica Kurz
Poaceae
29
Diploclisia glaucescens (Bl.)
Diels
Dregea volubilis (L. f.)
Benth. ex Hook.
Ficus fruticosa Roxb.
Menispermaceae
Moraceae
33
Ficus sarmentosa BuchananHamilton ex Smith
Flagellaria indica L.
34
Gouania leptostachya DC.
Rhamnaceae
35
Hoya parasitica Wall. ex
Wight
Asclepiadaceae
36
Convolvulaceae
38
Ipomoea obscura (L.) Ker
Gawler
Ipomoea pes-caprae (L.) R.
Brown
Ipomoea pes-tigridis L.
Convolvulaceae
39
Lygodium flexuosum (L.) Sw.
Lygodiaceae
40
Momordica charantia L.
Cucurbitaceae
41
Mucuna
DC.
(Willd.)
Papilionaceae
42
Mucuna monosperma DC. ex
Wight
Papilionaceae
43
Paramignya
andamanica
(King) Tan.
Plecospermum andamanicum
King
Raphidophora pertusa
(Roxb.) Schott
Scindapsus officinalis
(Roxb.) Schott
Stephania japonica (Thunb.)
Miers
Tetracera sarmentosa ssp.
andamanica (Hoogl.) Hoohl.
Tetrastigma
lanceolarium
(Roxb.) Planchon in A. & C.
DC.
Thunbergia laurifolia Lindley
Rutaceae
Tinospora cordifolia (Willd.)
Hook.f. & Thomson
Tylophora. indica (Burm.f.)
Merr.
Ventilago
madraspatana
Gaertn.
Menispermaceae
30
31
32
37
44
45
46
47
48
49
50
51
52
53
gigantea
33.33
91.67
2.39
2.07
2.92
2.44
7.43
8.25
16.67
16.67
0.87
1.04
0.53
0.1
1.67
6
41.67
58.33
1.22
2.59
1.86
0.31
4.76
3.36
25
66.67
2.32
1.55
2.12
3.93
7.61
10.67
16.67
41.67
2.17
1.04
1.33
1.73
4.09
15
8.33
25
2.61
0.52
0.8
0.03
1.34
36
33.33
75
1.96
2.07
2.39
2.46
6.91
6.75
41.67
75
1.56
2.59
2.39
0.02
4.99
4.32
25
58.33
2.03
1.55
1.86
0.01
3.42
9.33
33.33
50
1.30
2.07
1.59
0.01
3.67
4.5
25
66.67
2.32
1.55
2.12
0.02
3.69
10.67
16.67
58.33
3.05
1.04
1.86
0.01
2.90
21
25
41.67
1.45
1.55
1.33
0.01
2.89
6.66
8.33
25
2.61
0.52
0.8
1.01
2.31
36
16.67
33.33
1.74
1.04
1.06
1.38
3.47
12
16.67
25
1.30
1.04
0.8
1.04
2.87
9
25
25
0.87
1.55
0.8
1.37
3.72
4
16.67
25
1.30
1.04
0.8
0.31
2.14
9
25
25
0.87
1.55
0.8
0.02
2.37
4
58.33
66.67
0.99
3.63
2.12
0.53
6.27
1.95
16.67
33.33
1.74
1.04
1.06
0.51
2.61
12
8.33
16.67
1.74
0.52
0.53
0.13
1.18
24
66.67
116.7
1.52
4.15
3.71
0.23
8.09
2.62
25
83.33
2.90
1.55
2.65
0.2
4.40
13.33
1.33
24
Asclepiadaceae
Moraceae
Flagellariaceae
Convolvulaceae
Moraceae
Araceae
Araceae
Menispermaceae
Dilleniaceae
Vitaceae
Thunbergiaceae
Asclepiadaceae
100
133.3
1.16
6.22
4.24
0.43
10.8
9
8.33
16.67
1.74
0.52
0.53
1.15
2.19
Rhamnaceae
39
Indian Journal of Plant Sciences ISSN: 2319-3824 (Online)
An Online International Journal Available at http://www.cibtech.org/jps.htm
2013 Vol. 2 (3) July-September, pp.35-42/Ghosh
Research Article
Comparison of IVI of Species
30
y = 13.684e-0.0412x
R2 = 0.9416
Range of IVI
25
20
15
10
5
0
0
10
20
30
40
50
60
No. of Species
Figure 5: Comparison of IVI of littoral forest species
S & N1 (exp. of H')
Floral Species Diversity at Different Plots
50
40
30
20
10
0
1
2
3
S
4
N1
5
6
7
8
9
10
11
12
Plots
Figure 6: Comparison of species richness (S) and diversity (N1) of littoral forest plots
Figure 7: Dendogram of taxic similarity of littoral plots
In this vegetation, highest number of stems and species are found in the diameter classes of 5 cm to 6.99
cm. and 7- 8.99 cm. No stem has been recorded in 2-2.49 cm. and above 18 cm diameter classes; though
number of stems and species are appreciably high in the diameter classes of 0.5-0.99 cm and 1.5-1.99 cm.
Shannon Wiener Index (H’) showed that the plot numbers 2 and 3 show high species richness (S >_47),
the diversity of these plots are relatively high (N1> 15.15) in comparison to plot number 1, 4 and 5, where
species richness is high (S<28) but the diversity is relatively low (N1 >14.05). It is also found that the plot
numbers 7, and 12 show high diversity (N1 <10.42), but their species richness is low (S <17). Plots like 6,
8, 9, 10, and 11 show more or less proportionate S and N1 values (Figure 6).
It has been observed that the plots 6th and 10th, situated in the Paget-Point Island with the highest
taxonomic similarity (45.92593002) are similar to plot 2 nd (43.25204468). Plots 7th and 11th are quite far
from each other but they show relatively high similarity (40.68965912) and together with plots 1 st, 5th,
12th are more or less similar in species composition with similarity 39.16667175. 3 rd and 9th plots are in
different locations separated by sea and show poor similarity. Plot 8th is entirely of different composition
and is found as a separate cluster form the rest (Figure 7).
40
Indian Journal of Plant Sciences ISSN: 2319-3824 (Online)
An Online International Journal Available at http://www.cibtech.org/jps.htm
2013 Vol. 2 (3) July-September, pp.35-42/Ghosh
Research Article
ACKNOWLEDEMENT
The financial assistance from DBT-DOS is dually acknowledged. Special thanks are due to Prof. P. K.
Mukherjee and Dr. Krishna Chaudhuri, Department of Botany, Calcutta University.
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