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2011. Permit No. 2011-28.
Virginia R. Cardenas
Vice Chancellor for Community Affairs
University of the Philippines Los Baños
4031 College, Laguna, Philippines
Caliraya watershed was declared a forest reservation and protected area under Executive
Order No. 33 dated 26 July 1974. The area has its own special use as an upper
reservoir to support the water requirements of Caliraya and Kalayaan Hydroelectric
Plants in providing power sources in the Philippines. However, the Caliraya
Watershed is now degraded and polluted due to varying conflicting uses such as
agricultural food production, ecotourism, sports and recreation, home settlement
areas of informal settlers, resorts and rest houses development, and other multiple
uses. The increasing population within the watershed creates more pressure on the
natural resources, especially because alternative sources of sustainable livelihood are
unavailable. The human survival problems faced by the residents in the upstream and
downstream areas of the watershed had contributed to the degradation and pollution
of the area where the headwaters are located.
The intensive upland farming activities within the watershed areas have
created problems on soil erosion and consequent decline in farm production. Removal
of trees that used to prevent or minimize erosion has depleted the soil fertility,
resulting in poor productivity. For over a decade now, the watershed resources have
been overexploited because of the unlimited needs of the people living in the area.
Forested watersheds are converted into range and agricultural lands, tourist resorts
(e.g., Lagos del Sol and Caliraya Lake Ridge Resort), leisure parks (e.g., Trans-Caliraya
Integrated Areas Development (TCIAD) and Japanese Park), estates for villas, rest
houses, and subdivisions which cause environmental degradation, soil erosion,
flooding, landslide, and desertification.
Community vulnerability assessment to environmental changes 3
The inability of the watershed to meet the increasing demands for goods
and services threatens its sustainability. The continuous degradation of the watershed
would have significant impacts on the people, most specially the rural poor living
within and in the surrounding communities of Caliraya Watershed.
Objectives
Review of Literature
Vulnerability concept
The intensity of natural hazards such as floods and other phenomena have
exacerbated unsustainable environmental and resource use practices, including
deforestation, inappropriate land uses, and poor management of water resources.
These phenomena and other events often need to be assessed by the different
stakeholders, specifically the households, vulnerable groups, or community and other
concerned agencies and social institutions. A framework based on the P-S-I-R model,
which also includes vulnerability of the system to each type of pressures has been
developed (Rissik et al. 2003). A key feature of this framework is the identification
of the links between indicators of pressure, state, and impact, ensuring that only
indicators relevant to local situations are selected. In addition, a risk assessment
process has been developed (Fig.1), otherwise known as the Vulnerability-Pressure-
State-Impact-Risk-Response (VPSIRR).
Vulnerability Indicators
Pressures Condition
Risk
Management
Response Priority
Study area
A sample of 361 individuals from direct-impact sites was selected using simple
random sampling with confidence level of 95%. Interview schedule was developed
consisting of close and open-ended questions. Primary data were comprehensively
supplemented by several interviews with key informants randomly chosen from local
government agencies (LGAs), local government units (LGUs), NGOs, and private
institutions.
Statistical analyses
Both quantitative and qualitative methods were applied to analyze the data
using Statistical Program of the Social Science (SPSS). Descriptive statistics such as
frequency counts, percentages, and means were employed to determine the degree of
impacts of environmental changes; the vulnerability indicators (i.e., social, economic,
and biophysical); and the coping mechanisms.
Majority (69%) of the 361 respondents from five study sites were female,
relatively young (80%) aged 12 to 39 years old, married (69%), and had formal
education (97%), with an average of eight years stay in school or equivalent to second
year high school. Most households have an average number of two children attending
school. The average size of the family is five. The biggest family has 15 members.
More than half (58%) have only one member working for the family.
A large proportion (54%) of the respondents are native of the area while
the rest (46%) are local migrants. Respondents migrated to the area due to: marriage
(38.2%), employment (24%), the place was the residence of their parents (13%), and
more opportunities in the area (12%). Average year of residency is 23.8 years.
Majority (80%) of the respondents do not own the land they are cultivating
while 73% are informal settlers. One-third (30%) of the respondents had obtained a
title or tax declaration, 0.6% are lessees, and 3% are caretakers of the land they use.
Majority (61%) own less than 500 m2 of land and about 14% own 1,000 to 6,000 m2
of land. Average area of land ownership is 1,036.36 m2.
Of the farmer-respondents, majority (77%) do not own the land they cultivate while
23% titled their own land. More than half (55%) are informal occupants/squatters who cultivate
the land while 25% are owners who farm their own land. Only 11% of them are lessees.
More than two-thirds (69%) of the respondents are not aware of any information
and technology on the watershed. Those who are aware acquired information and
technology on methods of forest production (31%) and conservation (77%) and
different farming methods (11%). Thirty nine percent of the respondents who are not
aware of the information and technology pointed out that the technical personnel
from the government and other agencies do not provide them such information or no
such information or news has been disseminated (17%) at all.
8 A. S. Jose and V. R. Cardenas
Scale: Rating:
1 – Strongly Disagree (SD) 0.00 - 1.66 = Low
2 – Disagree (D) 1.67 - 3.35 = Neutral
3 – Fairly Agree (FA) 3.36 - 5.00 = High
4 – Agree (A)
5 – Strongly Agree (SA)
9
Table 2. Perception on the macro/micro impacts of environmental changes on the community. 10
Shared Perception (N=361)
Driver/Pressure Very Low Low Fair High Very High Weighted
Mean
F % F % F % F % F %
Social and Economic
Loss of life 23 6.4 104 28.8 43 11.9 164 45.4 27 7.5 3.19
Human injury 46 12.7 121 33.5 61 16.9 123 34.1 10 2.8 2.81
Insecurity of land tenure 95 26.3 128 35.5 35 9.7 97 26.9 6 1.7 2.42
Increased health problem 14 3.9 92 25.5 39 10.8 158 43.8 58 16.1 3.43
and causes of diseases
Loss of income and 13 3.6 96 26.6 71 19.7 150 41.6 31 8.6 3.25
livelihood
Loss of employment 9 2.5 91 25.2 112 31.0 141 39.1 8 2.2 3.13
Loss of business and 10 2.8 92 25.5 126 34.9 125 34.6 8 2.2 3.08
market
Weighted Mean 3.04
Adjective Rating High impact
Environmental
Degradation of 7 1.9 77 21.3 132 36.6 32 8.9 113 31.3 3.46
the environment
Extinction of natural 7 1.9 80 22.2 137 38.0 47 13.0 90 24.9 3.12
resources
Pollution 1 0.3 30 8.3 150 41.6 168 46.5 12 3.3 3.44
A. S. Jose and V. R. Cardenas
Table 2. Continuation...
Physical
Low power supply 3 0.8 68 18.8 145 40.2 62 17.2 83 23.0 3.43
Damage of dam, 8 0.8 61 16.9 153 42.4 73 20.2 71 19.7 3.42
infrastructure and
facilities
Weighted Mean 3.43
Adjective Rating Very high impact
Overall Weighted Mean 3.18
Community vulnerability assessment to environmental changes
Scale: Rating:
1 – Very low (VL) 0.00 - 1.66 = Least impact
2 – Low (L) 1.67 - 3.35 = High impact
3 – Fair (F) 3.36 - 5.00 = Very high impact
4 – High (H)
5 – Very high (VH)
11
12 A. S. Jose and V. R. Cardenas
Environmental impacts
Physical impacts
Physical impacts of environmental changes in the watershed consist of
damage to housing and properties, farmlands, dams and other infrastructures and
Community vulnerability assessment to environmental changes 13
facilities, and unforeseen hazards. Table 3 shows that the overall perception of the
respondents on the physical impacts is “high”. It was noted that unforeseen and
unavoidable accidents were perceived to be highly possible to occur more. Damage
on the physical structures, assets, and their houses are another potential impact to
which they thought they are susceptible.
Social vulnerability
Economic vulnerability
Unavoidable/unforeseen hazards 64 17.7 55 15.2 114 31.6 123 34.1 5 1.4 2.86
Weighted Mean 2.57
Adjective Rating High impact
Overall Weighted Mean 2.58
Adjective Rating High impact
Scale: Rating:
1 – Very low (VL) 0.00 - 1.66 = Least impact
2 – Low (L) 1.67 - 3.35 = High impact
3 – Fair (F) 3.36 - 5.00 = Very high impact
4 – High (H)
5 – Very high (VH)
15
Table 4. Extent of social vulnerability to environmental changes in the watershed, N=361. 16
Very Moderately Highly Very Highly Weighted
Social Factors Inadequate
Inadequate Adequate Adequate Adequate Mean
Adjective
F % F % F % F % F %
Description
Tenure system 123 34.1 66 18.3 109 30.2 57 15.8 6 1.7 2.33/ Highly
vulnerable
Basic needs of the family 117 32.4 64 17.7 164 45.4 11 3.0 5 1.4 2.33/ Highly
vulnerable
Susceptibility to hazards 122 33.8 109 30.2 107 29.6 21 5.8 2 0.6 2.09/ Highly
vulnerable
Overall Weighted Mean 2.29
Adjective Rating Highly Vulnerable
Scale: Rating:
1 - Very Inadequate 0.00 - 1.66 = Least Vulnerable
2 - Inadequate 1.67 - 3.35 = Highly Vulnerable
3 - Moderately Adequate 3.36 - 5.00 = Very Highly Vulnerable
4 - Highly Adequate
5 - Very Highly Adequate
A. S. Jose and V. R. Cardenas
Community vulnerability assessment to environmental changes 17
Biophysical vulnerability
The overall assessment of the respondents was that the community was
highly vulnerable (mean=2.63) to environmental changes (Table 7). Almost half of
them (49%) rated community vulnerability as moderate/fair while 35% rated it as
high.
Adjective
F % F % F % F % F %
Description
Income and livelihood 125 34.6 65 18.0 149 41.3 12 3.3 10 2.8 2.22/ Highly
Vulnerable
Employment 119 33.0 61 16.9 152 42.1 21 5.8 8 2.2 2.27/ Highly
Vulnerable
Productivity for home 73 20.2 118 32.7 104 28.8 63 17.5 3 0.8 2.46/ Highly
consumption Vulnerable
Overall Weighted Mean 2.24
Adjective Rating Highly Vulnerable
Scale: Rating:
1 - Very Low (VL) 0.00 - 1.66 = Least Vulnerable
2 - Low (L) 1.67 - 3.35 = Highly Vulnerable
3 - Fair (F) 3.36 - 5.00 = Very Highly Vulnerable
4 - High (H)
5 - Very High (VH)
A. S. Jose and V. R. Cardenas
Table 6. Extent of biophysical vulnerability exposing the watershed and community to hazard, shared perception
(N=361).
The environment and natural 14 3.9 182 50.4 165 45.7 4.42
resources are exploited and
degraded because of unsustainable
livelihood and income of the family.
Most upland areas have no forest 1 0.3 3 0.8 14 3.9 203 56.2 140 38.8 4.32
cover because of cutting of trees,
Community vulnerability assessment to environmental changes
Improper method of farming has 1 0.3 1 0.3 45 12.5 180 49.9 134 37.1 4.23
contributed to soil loss and erosion.
Deforestation is increasing fast, 1 0.3 2 0.6 23 6.4 167 46.3 168 46.5 4.38
causing scarcity in the water supply
for domestic use, irrigation, power
generation, and other uses.
19
Table 6. Continuation... 20
Environmental consequences 2 0.6 4 1.1 49 13.6 165 45.7 141 39.1 4.22
such as flooding, landslide and
man-made disasters are caused by
human activities and economic
development.
Poor water quality changes are due 22 6.1 148 41.0 191 52.9 4.47
to human activities and economic
development.
Overall Weighted Mean 4.35
Adjective Rating Very Highly Vulnerable
Scale: Rating:
1 – Strongly Disagree (SD) 0.00 - 1.66 = Least Vulnerable
2 – Disagree (D) 1.67 - 3.35 = Highly Vulnerable
3 – Fairly agree (FA) 3.36 – 5.00 = Very Highly Vulnerable
4 – Agree (A)
5 – Strongly Agree (SA)
A. S. Jose and V. R. Cardenas
Community vulnerability assessment to environmental changes 21
Table 9 shows the percentage and the kind of assistance provided by different
social institutions to reduce the negative impacts of environmental changes. Two-
thirds (66.6%) of the respondents stated that there were no provisions from different
social institutions to reduce the negative impacts of environmental changes in the
community.
22 A. S. Jose and V. R. Cardenas
Frequency
Response Percentage
(N=361)
Yes 41 11.4
No 320 66.6
Social institutions
Nongovernment organizations 32 78.2
(Jaycees, Couples for Christ,
and other religious groups)
Local government units 21 51.2
Local government agencies 6 14.6
(NPC, ERDB, etc.)
* Multiple responses
Table 11. Respondents’ recommended ways and means for different social
institutions in the community to reduce the impacts of environmental
changes.
Conclusion
The community vulnerability assessment recognizes that people and
community are susceptible to the impacts of environmental changes, thus, their
capacity (or lack thereof) to prepare, cope, and recover if such hazards occur needs
to be identified. The determinants of community vulnerability are: characteristics of
individuals, social-psychological behaviors of household and community, perceived
degrees of impact of environmental changes, response coping mechanisms, and the
state of vulnerability in the dimension of social, economic, and biophysical aspects.
Recommendations
These findings raised some significant issues and concerns for immediate
action and response coping mechanisms to mitigate and reduce the state of
vulnerability of the people and the community. The priority concerns include
sustainable environmental livelihood and agroforestry projects and activities, using
high value crops and fruit trees, among others. In improving the efficiency of economic
relations, social capital can help increase people’s income and their productivity for
home consumption.
Acknowledgement
This article is part of the completed thesis dissertation of the first author entitled
”Community Vulnerability Assessment to Environment Changes in Caliraya Watershed, Laguna,
Philippines” supported by the Southeast Asian Regional Center for Graduate Study and Research
in Agriculture (SEARCA) and Philippine Council for Agriculture, Forestry and Natural Resources
Research and Development (PCARRD). The authors also wish to express their gratitude to the
advisory committee composed of Dr. Federico A. Cruz, Dr. Elvira S. Talatayod and Dr. Antonio
J. Alcantara for their unwavering support and guidance in undertaking this research.
Literature cited
Bricker, S.B., J.G. Fereira, and T. Simas. 2003. An integrated methodology for assessment of
estuarine trophic status. Ecological modeling.
Bornales, R.G. 2004. Adaptation and vulnerability of Subanen community to the environmental
conditions in Mt. Malindang National Park, Philippines. Ph.D. dissertation. University of
the Philippines, College, Laguna.
Coligado, M.T. P.M. Baloaloa, B. Angeles, N. Madera, A. Gonzalvo, and L. Arce. 2004.
Integrated management plan for Caliraya-Lumot Watershed. UP Los Baños.
Downing, T.E. and Patwardhan. 2003. Vulnerability assessment for climate adaptation. APF
Technical Paper 3, United Nations Development Program, New York City, NY. Final Draft.
Lasco, R.D., J.M. Pulhin, R.V.O. Cruz, F.B. Pulhin, K.B. Garcia, R. Buer, and E.S. Wahyl.
2006. An integrated assessment of climate change impacts, adaptation and vulnerability
in watershed areas and communities in Southeast Asia. Environment Forest Program. UP
Los Baños.
28 A. S. Jose and V. R. Cardenas
Leurs, A.L., D.B. Lobell, L.S. Sklar, C.L. Addams, and P.A. Matson. 2003. A method for
quantifying vulnerability, applied to the Yaqui Valley, Mexico. Global Environment
Change 13.
McCarthy, J.J., O.F. Canzaiani, N.A. Leary, D.J. Dokken, and K.S. White. (Eds) 2001. Climate
change impact, adaptation and vulnerability. Cambridge University Press.
Philippine Council for Agriculture, Forestry and Natural Resources Research and Development
- University of the Philippines Los Baños. 1999. Guidelines for watershed management
and development in the Philippines. University of the Philippines, Los Baños, College,
Laguna.
Rissik, D., M. Cox, A. Moss, D. Ross, D. Scheltinga, L.T.H. Newham, A. Andress and S.C.
Baker-Finch. 2003. VPSIRR (Vulnerability-Pressure-State-Impact-Risk and Response):
An approach to determine the condition of estuaries and to assess where management
responses area required. Department of Infrastructure, Planning and Natural Resources.
CRC for Coastal Zone, Estuary and Waterway Management. Environment Protection
Authority, Victoria. Australian University, NSW Resources Commission.
Turner, B.L., II, R.E. Kasperson, P.A. Matson, J.J. McCathy, R.W. Corell, L. Christensen, N.
Eckley, J.X. Kasperson, A. Leurs, M.L. Martello, C. Polsky, A. Pulsipher and A. Schiller.
2003. A framework for vulnerability analysis in sustainability science. PNAS, 100(4).
Sofio B. Quintana
Regional Technical Director
Department of Environment and Natural Resources
Region 3
Mt. Banahaw is a rainforest mountain with an average of 262 rainy days per year. It
is a watershed that sustains water for the creeks, rivers, and falls draining to Laguna
de Bay and Tayabas Bay. These bodies of water sustain the domestic, irrigation, and
recreation needs of people living near the area. Many people believe that some of the
rivers have “healing power”, thus, they dip into the water believing that their illnesses
will be cured. The forest of Mt. Banahaw is an important refuge for many species of
plants and animals which act as protectors of watersheds. As a watershed, it provides
water to over a million people living in the provinces of Quezon and Laguna (Gascon
2002). This watershed also plays a very crucial ecological role in soil and water
conservation.
There are many studies conducted regarding the floristic composition of Mt.
Banahaw. These studies were encoded in a database for Mt. Banahaw. However, no
study was ever conducted focusing on the riparian zones. Since Mt. Banahaw is a
watershed with many tributaries contributing to the main river, it is very important
to know its floristic composition and physiognomy. Furthermore, according to
the Environmental Research Development Proceedings (1998), forest depletion
is connected to global warming and other climatic factors. A comprehensive and
accurate inventory is important because of the very incomplete and inadequate
knowledge on natural vegetation and of flowering plants. Therefore, basic floristic
study of the area is necessary.
The result of the study will contribute to the list of endangered and threatened
flora species in Mt. Banahaw. It could also provide additional information on the Mt.
Banahaw database. Particularly, it will give some insights and baseline data for the
proposed study of flora and fauna on the major rivers in the said protected area. It
could likewise serve as a basis in making policies regarding biodiversity conservation
of the landscape.
Tree species composition and physiognomy 31
Objectives
The study was conducted to determine the tree species composition and
physiognomy of Kinabuhayan River riparian zones, Mt. Banahaw-San Cristobal
Protected Landscape. Specifically, it attempted to determine the: 1) tree species
growing on the banks of Kinabuhayan River; 2) dominant species associations
at different elevations of the River; 3) differences in terms of species richness per
elevation; and 4) structure of the forest in the area.
Review of Literature
Forests provide huge benefits. Aside from supplying wood and other
products, they store a vast amount of genetic information, regulate the climate and
flow of water, protect and enrich the soils, control pests and diseases, pollinate useful
plants and disperse their seeds, safeguard water quality, offer beautiful landscape,
and enrich us spiritually (Kaimowitz 2002). They provide a wide range of economic,
social, cultural, and environmental benefits and services, including food, medicine,
and shelter. Forests are also protectors of watersheds. Trees trap the large amounts of
carbon dioxide that contributes to global warming (Enger and Smith 1998).
Riparian forests border streams, rivers, and lakes which occasionally include
emergency flood drainage areas. These areas absorb storm runoff, provide valuable
wildlife habitat, and are often used for picnic sites and hiking or nature trails (Grey
1996). According to Mortimer and Mortimer (1996), forested areas along the streams
fulfill other needs of the community at large by sorting water and by helping prevent
stream bank erosion, which in turn decreases sedimentation downstream. These
areas protect and enhance the aquatic environment as well. Shading the water keeps
it cooler, an essential condition for many desirable aquatic species. Buffer strip also
provides wildlife habitat and can be managed for special forest products.
Enger and Smith (1998) stated that deforestation significantly impacts climate.
If the trees are removed, flooding is more common and much valuable water is lost as
runoff. Riverbanks have special erosion problems as water level often changes, leaving
greater parts of the banks exposed, which are generally bare of vegetation. The most
32 A. E. Almazol and S. B. Quintana
severe kind of erosion is caused in streams carrying bedload. Most vulnerable are the
outside curves, where the flow is scouring and undercutting the banks.
The sampling area was confined to the Kinabuhayan River riparian zone
approximately located between the geographic coordinates of 14o02’02” North
latitudes and 121o26’42” to 121o27’27” East longitudes. Dolores, Quezon belongs to
Climatic Type II. It is characterized by pronounced maximum rain period from August
to December without any dry season. It lies at river altitude between 400 masl and
800 masl. Only 3.15 km of Kinabuhayan River was subjected to the study. The total
length of the river was not determined because of the limited capacity of the authors
to know its boundaries. Moderate to steep slopes, narrow channel, and vertical cliffs
on both sides of the river characterized the area.
Research procedure
Figure 1. Location map of Mt. Banahaw-San Cristobal Protected Landscape [Gascon 2002 (left) Mallari et al.
undated (right)].
33
34 A. E. Almazol and S. B. Quintana
Global Positioning System (GPS) was used in determining the geographic
location and elevations. Box compass was used for bearing determination of each
tree sampled. Meter tape was used in measuring distance and quadrat establishment,
diameter tape for diameter measurement, and Abney hand level for height determination.
Species collection was done for herbarium/voucher specimen and further
identification. Identification was done through comparing available illustrated works
and utilization of taxonomic keys and references such as literature and manuals.
Further validation was done with an expert. For vertical and horizontal diagram of
the forest, box compass was used to get the bearing of each tree and the diameter tape
for the diameter at breast height (dbh). Distance from plant to plant and the length
and width of the crown on its four coordinates were measured and determined using
meter tape. The data gathered from each plot were plotted and drawn to scale in an
illustration showing the overall appearance of the forest for each elevation.
Data analysis
Tree species compositions at different elevations were analyzed using
Sorenson’s formula for index similarity (Castillo 2001). The index has the following
formula:
CS = 2j
(a+b)
D = __1__
∑ (Pi)2
Where: D = Diversity
Pi = Proportion of species i in the total sample
Tree species composition and physiognomy 35
individuals. These species were typical in the forest habitat found at low and medium
altitudes ascending to 1,350 m.
The presence and importance of the following trees suggest that the
trees in the area are remnants of the primary trees. These are: 1) Sanglai (Ahernia
glandulosa Merr.) Flacourtiaceae; 2) Parugan [Endocomia macrocoma (Miq.)] de
Wilde ssp. prainii (King) de Wilde) Myristicaceae; 3) Binuang [Octomeles sumatrana
(Miq.)] Datiscaceae; 4) Balukanag [Chisocheton cumingianus (C.DC.)] Harns.
ssp. cumingianus) Meliaceae; 5) Magabuyo (Celtis luzonica Warb.) Celtidaceae;
6) Balumti (Macaranga dipterocarpifolia Merr.) Euphorbiaceae; 7) Philippine maple
(Acer laurinum Hassk. Apud Hoeven and de Vriese) Aceraceae; 8) Anongong isahan
(Turpinia simplicifolia Merr.) Staphyleaceae; and 9) Bagtikan [Parashorea malaanonan
(Blanco) Merr.]. Presence of Dipterocarpaceae suggests that the trees in the area are
remnants of primary forest. Binuang [Octomeles sumatrana (Miq.)] Datiscaceae and
the Moraceae Family represented by genus Ficus also thrive in primary forest along
streams and moist areas of low and medium altitudes (Rojo 1999).
The two species with higher IV at 400-500 masl were Bagtikan [Parashorea
malaanonan (Blanco) Merr.] Dipterocarpaceae and Moluccan sau (Albizia
falcataria) Leguminosae. At 500-600 masl the dominants were Balumti (Macaranga
dipterocarpifolia Merr.) Euphorbiaceae and Balukanag (Chisocheton cumingianus
(C.DC.) Harns. subsp. cumingianus) of Meliaceae. At 600-700 masl, it was found
out that Loktob (Duabanga moluccana Blume) of Sonneratiaceae dominated the
area. It was associated with Philippine maple (Acer laurinum Hassk.) of Aceraceae.
Sanglai (Ahernia glandulosa Merr.) of Flacourtiaceae and Anongong isahan (Turpinia
simplicifolia Merr.) of Staphyleaceae were found associated with each other at 700-
800 masl.
Species diversity
Species diversity generally refers to the number of species (species richness
and species variety) and the distribution or proportion of individuals among species
Table 1. List of tree species found along Kinabuhayan River riparian zone.
Forest physiognomy
Diameter classes
Height classes
Generally, more trees belonged to 11-20 m height class as observed from
three elevations except on 600-700 masl (Fig. 4). The trend is decreasing showing
lesser number of individuals with 21-30 m and 31-40 m above height classes. It
is indicative of periodic disturbances in the area. The presence of high number of
individuals with 21-30 m height class at 600-700 masl indicate preservation activities
in the area. The people in the area reserved or left those trees uncut for future use.
Trees with this height belong to only one species, the Loktob (Duabanga moluccana
Blume). It is noteworthy that the species were found in group.
Horizontal structure
Bagtikan [Parashorea malaanonan (Blanco) Merr.] of Dipterocarpaceae and
Binuang [Octomeles sumatrana (Miq.)] of Datiscaceae were the largest trees present
on the two elevations at 400-500 masl (Fig. 5) and 500-600 masl (Fig. 6), respectively.
These two species have the largest crown area which overshadows the other species.
These areas were characterized by steep slopes wherein overcrowding of species was
possible, hence, the canopy overlaps. At elevation 600-700 masl (Fig. 7) and 700-800
44 A. E. Almazol and S. B. Quintana
Vertical structure
At 400-500 masl (Fig. 9) and 500-600 masl (Fig. 10), few individuals
dominated the area overshadowing all the other species. Considering its horizontal
structure, it has been stated previously that these species were the Bagtikan [Parashorea
malaanonan (Blanco) Merr.] of Dipterocarpaceae and Binuang [Octomeles sumatrana
(Miq.)] of Datiscaceae. At elevations 600-700 masl (Fig. 11) and 700-800 masl (Fig. 12),
stratifications were very different from the two lower elevations. More trees belong to
co-dominant and intermediate species, implying that the trees exhibited larger crown
canopy length, width, and diameter because of its greater exposure to sunlight. The solar
radiation determines the “condition of existence” to which organisms most adapt. The
solar energy received by the green plants contributes to the ecosystem’s productivity
(Odum 1971).
Tree species composition and physiognomy
Conclusions
Within the conditions under which the study was conducted, the following
conclusions were formed:
1. The tree species composition is typical to forests found at low and medium
altitudes ascending to 1,350 m. They are represented with species thriving in
primary forests along streams and moist areas at low and medium altitudes.
Recommendations
Based on the results of the study, the following recommendations are hereby
made:
calantas Merr. & Rolfe); and Anuling (Pisonia umbellifera) (J. R. et. G. Forster
Seem). These could be later used for research purposes.
4. Other studies dealing with faunal composition should also be done in the
study area and in the riparian zones of other major rivers of Mt. Banahaw–San
Cristobal Protected Landscape.
5. The non-timber species thriving in the area should be known and their
economic value should be determined to ensure proper protection of the plant
community.
Acknowledgement
The authors express their gratitude to For. Ronald C. Garcia, Prof. Pastor Malabrigo,
SLSU College of Agriculture Faculty, Dr. Cecilia N. Gascon, and the SLSU for funding the research.
Literature cited
Castillo, M.C. 2001. Structure and floristic diversity of the vegetation on an ultramafic hill in
Surigao del Sur, Philippines. Ph.D. dissertation. UPLB, College of Forestry and Natural
Resources, College, Laguna.
Enger, E.D and B.F. Smith. 1998. Environmental Science: A study of interrelationships. 6th ed.
Mc Graw-Hill. 1010 pp.
Gascon, C.N. 2000. Manual in ecology. Southern Luzon Polytechnic College, Lucban,
Quezon. p 30.
Gascon, C.N. 2002. Mt. Banahaw: Physical, biological and management features. Foundation
for Philippine Environment, SYNRGOS, ASEAN Regional Center for Biodiversity
Conservation and Southern Luzon Polytechnic College, Lucban, Quezon. 98 pp.
Grey, G.W. 1996. The urban forest comprehensive management. John Wiley and Sons, Inc.
New York. 90 pp.
Tree species composition and physiognomy 55
Kaimowitz, D. 2002. Forest valuation: From science to fiction to money on the table. ASEAN
Biodiversity. 2(2): 10-15.
Kovach, W.L. 1998. Multivariate Statistical Package (MVSP) Version 3.0 for Windows. Trial
Version Software Program.
Mallari, N.A and A.C. Diesmos. Undated. Faunal diversity of Mt. Banahaw de Tayabas and
implications for conservation priorities. Haribon-Birdlife Philippines Programme Manila
and UPLB, College, Laguna.
Montimer, J. and M. Bunny. 1996. Shelter and shade: Creating a healthy and profitable
environment for our livestock with trees. Green Park Press, Jackson MS. 161 pp.
Mueller and Dombois and H. Ellenberg. 1974. Aims and methods of vegetation ecology. John
Wiley and Sons. New York. 547 pp.
Odum, E.P. 1971. Fundamentals of ecology. 3rd ed. Sanders Company. West Washington
Square, Philadelphia.
Richards, P.W. 1936. Ecological observations on the rainforest of Mt. Dulit, Saraoak. I. II, J.
Ecol. 24:1-37.
Rojo, J.P. 1999. A revised Lexicon of Philippine trees. FPRDI-DOST, College, Laguna.
Whittaker, R.H. 1960. Vegetation of the Siskiyou Mountain. Ecology Monong. 30:279-338.
56 A. E. Almazol and S. B. Quintana
Sylvatrop, The Technical Journal of Philippine Ecosystems and Natural Resources 19 (1 & 2): 57 - 80
Marine turtles are reptiles that live in the sea. Adult female turtles come up the beach to
lay eggs in isolated sandy beaches far from human interventions.
After reaching the age of sexual maturity (25-50 years), a marine turtle migrates
thousands of kilometers from its feeding area to its breeding area. One month after
mating, the female turtle comes up the beach to lay eggs. A nester can lay 80 to 120
eggs, three to five times in one nesting season with an internesting interval of 10 to
15 days. It is believed that a female turtle returns to lay eggs at the same beach where
she was hatched.
Five of the seven species of marine turtles in the world are present in the
Philippines. Three of the five species were found to nest in the Philippine coastal areas.
These are the green turtle (Chelonia mydas) (Fig. 1), hawksbill turtle (Eretmochelys
imbricata) (Fig. 2), and the olive ridley turtle (Lepidochelys olivacea) (Fig. 3). The
loggerhead (Caretta caretta) (Fig. 4) and leatherback turtles (Dermochelys coriacea)
(Fig. 5) forage in Philippine waters.
Since early 1980s, surveys have been conducted by the Pawikan Conservation
Project (PCP) to identify nesting sites of marine turtles in the Philippines. Some of the
identified nesting beaches declared as marine turtle sanctuaries have been managed
solely by the DENR. Unfortunately, in the late 1980s to early 1990s, marine turtle nests
which are laid in other nesting beaches were not totally monitored and protected.
To conserve marine turtles, both the species and habitat need to be protected.
Management of identified nesting beaches is, thus, very vital. In the Philippines, the
DENR through the PCP of the Protected Areas and Wildlife Bureau (PAWB) is tasked
to implement a nationwide conservation and protection program on marine turtles.
One major activity of the project is the survey of nesting beaches nationwide. In each
identified nesting beaches, joint DENR-LGU community-based conservation projects
will be carried out.
This paper aims to provide a basis in tapping the assistance of LGUs with
identified nesting sites to participate and support the marine turtle conservation
program of the DENR.
Review of Literature
Nesting beach survey refers to the ground and/or aerial surveys conducted to
gather information on the number of nesting and non-nesting emergences occurring
on a beach. Nesting beach surveys are the most widely implemented monitoring tool
employed by researchers at different nesting beaches across the globe and are an
important component of a comprehensive program to assess and monitor the status
of sea turtle populations (Schroder and Murphy 1999).
62 A. T. Viloria
Interpreting other data such as relevant physical features of the nesting beach
can be generalized. The different species of marine turtles have different nesting
beach preferences. Green turtles nest in open habitat with white sandy beaches.
The hawksbills traverse rocks or shallow coral rubbles to nest in heavily vegetated,
low profile beaches. The olive ridleys prefer to nest on beaches separated from the
mainland by coastal lagoons or estuaries (Diez and Ottenwalder 1999).
Once the survey results are complete, identified nesting habitats should be
regularly monitored and a conservation plan should be designed and implemented.
The overall goal of any conservation plan for marine turtles is to promote
the long-term survival of their populations, including the sustained recovery of their
depleted stocks and the safeguarding of critical habitat integrated with the well-
being and needs of human communities with which they interact (Eckert 1999).
Specific objectives should include: 1) identification of nesting/breeding sites, 2)
identification of population and regular monitoring to assess the trends, 3) assessment
of the conservation status of the population throughout their range, 4) identification
and quantifying of important sources with direct and indirect mortality, 5) effective
protection of nesting beaches and migratory corridors, and 6) achieving public support
for program goals and objectives.
Over the years, some local government officials have come to recognize that
marine turtles are shared resources that require shared responsibility. Cooperative
mechanisms are required in managing shared resources. Thus, for a conservation
program to succeed, every effort must be made to involve all relevant sectors and
stakeholders in planning and, ultimately, in implementing activities (Eckert 1999).
Survey of marine turtle nesting sites 63
Methodology
Sites were selected based on reports submitted by DENR Regional and Field
Offices, LGUs, NGOs, POs, and concerned citizens. Three to four municipalities that
were reported as nesting sites were selected per year. A team, composed of two to
three personnel from the PCP, assisted by one or two personnel from DENR Regional
and/or Field Offices, conducted the survey.
The survey involved interviews of key informants using the form on habitat
survey of marine turtles. Key informants include fishermen or residents who personally
encountered nesting marine turtles in their area. Key informants were asked on the
specific location, month, and species of marine turtles that nested in their locality.
Data included in the report were supported by evidences such as photographs, eggs,
egg shells, live turtle hatchlings, hatchlings found dead in nest, pipped eggs, and
unhatched eggs.
The data pertaining to nesting sites were tabulated in the habitat survey forms
after each activity. Table 1 and Figures 6-8 present the area and geolocation of the
nesting beach by region including the species that nest in each site.
Region IV-B has the most number of confirmed nesting beaches among all
the regions.
Turtle Islands in Tawi-Tawi has been declared as the Turtle Islands Wildlife
Sanctuary (TIWS) pursuant to Presidential Proclamation No. 171, dated 26 August
1999.
Today, partners of the DENR on marine turtle conservation include Bagac and
Morong in Bataan, coastal areas of Zambales Province, Lian in Batangas, Magsaysay
in Misamis Oriental, Davao City in Davao del Sur, Island Garden City of Samal in
Davao del Norte, and Hinatuan in Surigao del Sur. Partnerships were formalized
either through a Memorandum of Agreement (MOA) or MOU.
Table 1. List of confirmed marine turtle nesting beaches in the Philippines from 1992-2007. 64
Olive ridley
3 So. Gantuan, Brgy. Nagbalayong, Morong, Bataan 120º 3170’E; 14º 6370’N Olive ridley
3 Cabayo, llog, Bagac, Bataan 120º 3600’E; 14º 6300’N Olive ridley
3 Cabayo, Beach, Banawang, Bagac, Bataan 120º 3800’E; 14º 6100’N Olive ridley
3 Acuzar Beach, Brgy. Pag-asa, Bagac, Bataan 120º 3800’E; 14º 6000’N Olive ridley
3 Brgy. Pag-asa, Bagac, Bataan 120º 3868’E; 14º 5959’N Olive ridley
3 Saysain, Bagac, Bataan 120º 3900’E; 14º 5600’N Olive ridley
3 Caybobo, Brgy. Paysawan, Bagac, Bataan 120º 3900’E; 14º 5400’N Olive ridley
3 Paysawan, Bagac, Bataan 120º 3890’E; 14º 5350’N Olive ridley
Hawksbill & Olive
3 Brgy. Quinawan Beach, Bagac, Bataan 120º 3800’E; 14º 4900’N
ridley
3 So. Aniasan, Quinawan, Bagac, Bataan 120º 3900’E; 14º 4780’N Hawksbill
3 Tangos ni Apo Purong, Brgy. Qiunawan, Bagac, Bataan 120º 3900’E; 14º 4780’N Hawksbill
3 Mauakis, lpag, Mariveles, Bataan 120º 4600’E; 14º 4100’N Hawksbill
3 Batangas ll, Mariveles, Bataan 120º 6000’E; 14º 4900’N Hawksbill
3 Looc Beach, Cabayo, Banawang, Bagac, Bataan 120º 3800’E; 14º 6100’N Olive ridley
4A Julugan Vll, Tanza, Cavite 120º 8400’E; 14º 4000’N Olive ridley
65
4A Fortune lsland, Nasugbu, Batangas 120º 4899’E; 14º 0542’N Green & Hawksbill 66
4A Munting Buhangin Beach, Brgy. Natipuan, Nasugbu, Batangas 120º 6200’E; 14º 1200’N Olive ridley
4A Brgy. Wawa, Nasugbu, Batangas 120º 6300’E; 14º 0900’N Olive ridley
4A Brgy. Bucana, Nasugbu, Batangas 120º 6200’E; 14º 0700’N Olive ridley
4A San Diego, Lian, Batangas 120º 6230’E; 14º 0410’N Olive ridley
4A Brgy. Lumaniag, Lian, Batangas 120º 6200’E; 14º 0000’N Green
4A So. Matuod, Brgy. Binubusan, Lian, Batangas 120º 6300’E; 13º 9700’N Green & Olive ridley
4A Brgy. Camastilisan, Calaca, Batangas 120º 8100’E; 13º 9300’N Olive ridley
4A Brgy. Salong, Calaca, Batangas 120º 8200’E; 13º 9200’N Olive ridley
4A Brgy. Nonong Casto, Lemery, Batangas 120º 8900’E; 13º 9000’N Olive ridley
4A Brgy. Sta. Rita, Aplaya, Batangas City, Batangas 121º 0294’E; 13º 7688’N Olive ridley
4A So. Biga, Brgy. Hugom, San Juan, Batangas 121º 3700’E; 13º 6700’N Hawksbill
4A Brgy. Laiya Aplaya, San Juan, Batangas 121º 3900’E; 13º 6800’N Olive ridley
4A Brgy. Laiya lbabaw, San Juan, Batangas 121º 4200’E; 13º 6700’N Olive ridley
4A Brgy. Calubcub 2, San Juan, Batangas 121º 4300’E; 13º 7400’N Olive ridley
4A Brgy. Abung, San Juan, Batangas 121º 4200E’; 13º 7700’N Olive ridley
4A Brgy. Tikalan, San Juan, Batangas 121º 4300’E; 13º 7900’N Olive ridley
4A Brgy. Pinagbayanan, San Juan, Batangas 121º 4400’E; 13º 8000’N Olive ridley
4A Tayabas Bay, Brgy. San Roque, Sariaya, Quezon 121º 5200’E; 13º 8700’N Olive ridley
4A Brgy. Caridad llaya, Atimonan, Quezon 121º 9100’E; 14º 0200’N Hawksbill
4A Brgy. Ibabang Kalilayan, Unisan, Quezon 121º 9600’E; 13º 8500’N Olive ridley
Las Villas de Natividad Resort, Aninuan, Puerto Galera,
4B 120º 9000’E; 13º 5400’N Green
Oriental Mindoro
Anahaw lsland View Resort, Brgy. Balete, Calapan, Oriental
4B 121º 1603’E; 13º 4145’N Olive ridley
Mindoro
A. T. Viloria
4B Sugui, Calapan, Oriental Mindoro 121º 2070’E; 13º 4190’N Olive ridley
4B Guimbonan, Gloria, Oriental Mindoro 121º 4920’E; 12º 9260’N Green
4B Purok Malvar, Brgy. Pag-asa, San Jose, Occidental Mindoro 121º 0800’E; 12º 3500’N Green
4B So. Tabuk, Buenavista, Sablayan, Occidental Mindoro 120º 7900’E; 12º 8600’N Green & Olive ridley
4B Punta Poblacion, Sablayan, Occidental Mindoro 120º 7760’E; 12º 8340’N Green
4B Apo Reef Natural Park, Sablayan, Occidental Mindoro 120º 4750’E; 12º 6830’N Green & Hawksbill
4B Brgy. Lupac, Boac, Marinduque 121º 8100’E; 13º 4600’N Green & Olive ridley
4B Brgy. Masiga, Gasan, Marinduque 121º 8200’E; 13º 3600’N Green
Survey of marine turtle nesting sites
4B Brgy, Mompong, Sta. Cruz, Marinduque 122º 1300’E; 13º 5500’N Green
4B Poctoy White Beach, Torrijos, Marinduque 122º 0920’E; 13º 3250’N Olive ridley
4B Centro Long Beach, San Agustin, Romblon 122º 1500’E; 12º 6300’N Hawksbill
4B Brgy. Tumingad, Odiongan, Romblon 122º 0000’E; 12º 4400’N Green
4B Brgy. Budiong, Odiongan, Romblon 121º 9700’E; 12º 4000’N Green
4B Ligaya Public Beach, Odiongan, Romblon 121º 9800’E; 12º 4000’N Green
4B Brgy. Batiano, Odiongan, Romblon 121º 9950’E; 12º 4260’N Green
4B Brgy. Lanas, San Jose, Romblon (Carabao lsland) 121º 9230’E; 12º 0450’N Hawksbill
Hawksbill & Olive
4B Brgy. Agpanabat, Romblon, Romblon 122º 2890’E; 12º 4800’N
ridley
4B Halog Island, Palawan 120º 52.051’E; 11º 22.407’N Green
4B Pamilacan Island, Cuyo, Palawan 120º 44.071’E; 11º 21.114’N Green & Hawksbill
4B Tanobon lsland, Busuanga, Palawan 119º 9550’E; 12º 3420’N Green & Hawksbill
4B Pag-asa lsland, Kalayaan, Palawan 116º 7100‘E; 10º 4900’N Green
4B Panata Cay, Kalayaan, Palawan 114º 2700’E; 10º 2100’N Green & Hawksbill
4B Kota Cay, Kalayaan, Palawan 114º 1800’E; 10º 1700’N Green & Hawksbill
67
4B So. Cagbatang, Pasadeña, El Nido, Palawan 119º 4200’E; 11º 2500’N Green 68
4B Sunset Beach, Cadlao lsland, Buena Suerte, El Nido, Palawan 119º 3600’E; 11º 2200’N Green
4B So. Pacalsada, Corong-corong, El Nido, Palawan 119º 4000’E; 11º 1600’N Hawksbill
4B Miniloc lsland, El Nido, Palawan 119º 3100’E; 11º 1500’N Olive ridley
4B Entalula lsland, Bacuit Bay, El Nido, Palawan 119º 3300’E; 11º 1300’N Hawksbill
4B Cudugnon Beach, Bebeladan, El Nido, Palawan 119º 3800’E; 11º 0400’N Hawksbill
Daluyon Beach, Sabang Cabayugan, Puerto Princesa City,
4B 118º 8000’E; 10º 1900’N Olive ridley
Palawan
4B Brgy. Simpokan, Puerto Princesa City, Palawan 118º 5270’E; 9º 8450’N Olive ridley
Sitio Tagminatay, Brgy. Bacungan, Puerto Princesa City,
4B 118º 6100’E; 9º 8900’N Olive ridley
Palawan
Nagtabon Beach, Brgy. Bacungan, Puerto Princesa City,
4B 118º 7450’E; 9º 9020’N Hawksbill
Palawan
4B Arena lsland, Narra, Palawan 118º 5000’E; 9º 2300’N Hawksbill
4B Antipuluan, Narra, Palawan 118º 4400’E; 9º 2800’N hawksbill
4B Purok Pag-asa, Brgy. Panacan, Narra, Palawan 118º 4400’E; 9º 2800’N Hawksbill
4B Purok Pagkakaisa, Brgy. Panacan, Narra, Palawan 118º 4140’E; 9º 2450’N Hawksbill
4B Tubbataha Reef Natural Park, Cagayancillo, Palawan 119º 9020’E; 8º 8490'N Green & Hawksbill
4B Brgy. Sablayan, Romblon, Romblon 122º 3272’E; 12º 5053’N Hawksbill
4B Brgy. Lunas, Romblon, Romblon 122º 2693’E; 12º 4986’N Hawksbill
5 Brgy. Guijalo, Caramoan, Camarines Sur 123º 8700’E; 13º 7400’N Green
5 Brgy. Talisoy, Virac, Catanduanes 124º 2290’E; 13º 5800’N Green
5 Brgy. Magnesia del Sur, Virac, Catanduanes 124º 1861’E; 13º 5238’N Green
5 Sagurong, San Miguel lsland, Tabaco, Albay 123º 7900’E; 13º 4000’N Green
5 Mosboron, Misibis, Bacacay, Albay (Cagraray) 123º 9000’E; 13º 2500’N Green
A. T. Viloria
5 Brgy. Rawis, Legaspi City, Albay 123º 7500’E; 13º 1700’N Green
5 Basud, Quidolog, Prieto Diaz, Sorsogon 124º 1960’E; 13º 0410’N Hawksbill
6 Panagatan lsland, Antique (Caluya) 121º 2900’E; 11º 8630’N Hawksbill
6 Brgy. Manoc-manoc, Malay, Aklan (Boracay lsland) 121º 9302’E; 11º 9499’N Hawksbill
6 Patria, Pandan, Antique 122º 0174’E; 11º 7427’N Hawksbill
6 Brgy. Lipata, Culasi, Antique 122º 0520’E; 11º 4660’N Hawksbill
6 Malalison ls. Culasi, Antique 122º 0120’E; 11º 4070’N Hawksbill
6 Aring Cadahug, Laua-an, Antique 122º 0400’E; 11º 1420’N Green
Survey of marine turtle nesting sites
6 So. Aring, Brgy. Bagumbayan, Laua-an, Antique 122º 0400’E; 11º 1000’N Green
6 Brgy. Arobo, Tobias Fornier, Antique 121º 9613’E; 10º 5646’N Green
6 Brgy. Crossing Dapuyan, San Juaquin, llo-ilo 122º 1500’E; 10º 6000’N Green
6 Ave Maria lslet, Punta Lawi, Jordan, Guimaras 122º 5150’E; 10º 5475’N Hawksbill
6 So. Guisi, Brgy. Dolores, Nueva Valencia, Guimaras 122º 5130’E; 10º 5340’N Hawksbill
6 Calumpang, Pob. Cauayan, Negros Occidental 122º 6200’E; 9º 9800’N Olive ridley
6 Brgy. Bulata, Cauayan, Negros Occidental 122º 4000’E; 9º 8570’N Green & Hawksbill
6 Brgy. Nauhang, Sipalay, Negros Occidental 122º 4020’E; 9º 7530’N Green & Hawksbill
6 Tabuk-suba, Brgy. 1, Hinobaan, Negros Occidental 122º 4620’E; 9º 6140’N Hawksbill
6 So. Panganawan, Brgy. Sangke, Hinobaan, Negros Occidental 122º 5761’E; 9º 4525’N Hawksbill
7 Alejawan, Jagna, Bohol 124º 4000’E; 9º 6800’N Hawksbill
7 Basdaku, Brgy. Saavedra, Moalboal, Cebu 123º 3860’E; 9º 9380’N Green & Hawksbill
7 Sandugan, Larena, Siquijor 123º 5959’E; 9º 2917’N Green
7 Poblacion, Candanay, Siquijor 123º 5100’E; 9º 2200’N Hawksbill
7 Solangon, San Juan, Siquijor 123º 4746’E; 9º 1737’N Hawksbill
7 Lipayo, Dauin, Negros Oriental 123º 1900’E; 9º 2200’N Hawksbill
69
7 Brgy. Maayong Tubig, Dauin, Negros Oriental 123º 1600’E 9º 1800’N Hawksbill 70
13 Singoroy lsland, Baculin, Hinatuan, Surigao del Sur 126º 3850’E; 8º 5410’N Hawksbill
ARMM Bancauan Island, Mapun, Tawi-Tawi 118º 5390’E; 7º 7610’N Green & Hawksbill
ARMM Baguan Island, Turtle Islands, Tawi-Tawi 118º 4600’E; 6º 1500’N Green & Hawksbill
ARMM Lihiman lsland, Turtle Islands, Tawi-Tawi 118º 0900’E; 6º 2400’N Green & Hawksbill
ARMM Langaan lsland, Turtle Islands, Tawi-Tawi 118º 1700’E; 6º 2200’N Green & Hawksbill
ARMM Taganak lsland, Turtle Islands, Tawi-Tawi 118º 3300’E; 6º 0900’N Green & Hawksbill
ARMM Limbayan, Bongo lsland, Parang, Maguindanao 124º 0316’E; 7º 3051’N Green
ARMM Langil lsland, Tuburan, Basilan 122º 3680’E; 6º 7580’N Green
A. T. Viloria
Survey of marine turtle nesting sites
Partnerships are being formalized with the LGUs of Sta. Maria and Vigan City
in Ilocos Sur; Casiguran and Dilasag in Aurora; Calaca, San Juan and Lobo in Batangas
City; Negros Occidental Alliances; Malita in Davao del Sur; and Maitum, Kiamba and
Maasim in Sarangani.
Recommendation
The data shown can be used as basis in initiating joint conservation measures
with other LGUs. Interested organizations or institutions can likewise carryout their
own conservation projects in coordination with the DENR.
Acknowledgement
Thank you to all the PCP staff and PAWCZMS staff of DENR-Regions 1, 3, 4A, 4B, 5,
6, 7, 9, 10, 11, 12, 13, and its Field Offices, and DENR-ARMM involved in the survey.
Literature Cited
DENR Regions 1, 2, 3, 4A, 4B, 5, 6, 7, 8, 9 10, 11, 12, 13, ARMM reports.
Diez, C.E. and J.A. Ottenwalder. 1999. Habitat surveys in Eckert, K.L. et al. 1999. Research
and management techniques for the conservation of Sea Turtles. IUCN/SSC Marine Turtle
Specialist Group Publication No. 4. pp. 41-44.
Eckert, K.L. 1999. Designing a conservation program in Eckert, K.L. et al. 1999. Research
and management techniques for the conservation of Sea turtles. IUCN/SSC Marine Turtle
Specialist Group Publication No. 4. pp. 6-9.
Internation Union for the Conservation of Nature and Natural Resources. Avail from: http://
www.iucnredlist.org/. The IUCN Red List of threatened species.
Mortimer, J.A. 1999. Reducing threats to eggs and hatchlings: Hatcheries in Eckert, K.L. et al.
1999. Research and management techniques for the conservation of Sea turtles. IUCN/
Survey of marine turtle nesting sites 79
Schroeder, B. and S. Murphy. 1999. Population surveys (ground and aerial) on nesting beaches
in Eckert, K.L. et al. 1999. Research and management techniques for the conservation of
Sea turtles. IUCN/SSC Marine Turtle Specialist Group Publication No. 4. pp. 45-55
Turtle Islands Wildlife Sanctuary Management Plan. 2008. Department of Environment and
Natural Resources, Quezon City, Philippines.
80 A. T. Viloria
Sylvatrop, The Technical Journal of Philippine Ecosystems and Natural Resources 19 (1 & 2): 81 - 102
Veronica O. Sinohin
Supervising Science Research Specialist
Technology Development Division
Ecosystems Research and Development Bureau
College, Laguna
Seed health testing using blotter test was conducted to detect and
identify insects and fungi associated with seeds of bungalon (Avicennia
marina) and api-api (A. officinalis) collected in four sites, namely: San Juan
and Lian, Batangas; Pagbilao, Quezon; and Las Piñas City, Metro Manila.
The most commonly observed seed-feeding insects were the fruit fly
(Bactrocera umbrosa Fabricius), snout beetle (Coleoptera: Curculionidae),
plume moth (Stenoptilodes sp.), noctuid moth (Lepidoptera: Noctuidae), and
tineid moth (Lepidoptera:Tineidae). Important morphological characters of
these five insect species were described and their host ranges, economic
importance, and distribution were listed.
With the massive and continuous loss of Philippine mangrove forests, the government
has embarked on various reforestation programs to replenish the dwindling mangrove
resources nationwide. One of the most promising mangrove reforestation species is
the Avicennia. Melana et al. (1991) considered Avicennia as a versatile characteristic
species due to its ability to coppice even if the meristems are cut. It produces profuse
seeds and tolerates climatic extremes. Nevertheless, the use of these species for
reforestation purposes does not always guarantee a remarkable success particularly
when their seeds and propagules are attacked by seed-invading organisms such as
insects, fungi, bacteria, virus or nematodes (Viado 1979; Sinohin et al. 1996). Among
these pests, insects and fungi are the most common.
In general, insects are the greatest destroyers of tree fruits and seeds. Insects
destroy seeds throughout all their reproductive stages by feeding from the developing
buds to the seeds in storage. This process reduces both the quality and quantity of
seeds of any plant (Bonner et al. 1994). Similarly, pathogens like fungi are a serious
threat to seed health because of the enormous numbers of species known as seed
pathogens that cause various kinds of seed damage, namely, seed abortion, shrinking
of seeds and seed rot, to name a few (Bonner et al. 1994). Any damage caused by
these agents during seed development causes poor germination and poses a serious
threat in planting stock production.
Review of Literature
Insect group
Among seed-destroying agents, insects are probably responsible for the most
serious losses. Insects are capable of attacking seeds on a mother tree (Viado 1979;
Hedlin and Eungwijarnpanya 1984), on the ground (Singh 1990; Kamnerdratana
1987), and in storage (Kamnerdratana 1987). Seed-feeding insects are classified by
Lapis (1984) into four categories based on the stage of seed development: 1) insects
which infest seeds while in storage; 2) species which feed in or on immature seeds; 3)
species which attack mature seeds; and 4) species which attack seeds after they have
been dispersed or sown in seedbeds.
At least five orders of insects infest the seeds of different forest tree
species in Southeast Asia. These orders are Coleoptera, Lepidoptera, Hymenoptera,
Hemiptera, and Homoptera. Coleopterans are the most destructive. They consist of
several families, namely: Bruchidae (Suratmo 1987, Singh 1990), Curculionidae (De
Mesa 1934, Tho 1987 and Akanbi and Odeyindi 1990), Scolytidae (Viado 1979,
Kamnerdratana 1987, Tho 1987, and Hutacharern 1990), Anthribidae (Viado 1979),
Meloidae (Kamnerdratana et al. 1987), Nitidulidae (Kamnerdratana et al. 1987),
and Apionidae (Hedlin and Eungwijarnpanya 1984). Among these families, seed
feeders belonging to family Bruchidae are the most common. The rest of the insect
orders are represented by a few families. Among Lepidopterans, species belonging
to families Pyralidae (Suratmo 1987, Tho 1987, Natawiria 1990 and Singh 1990),
Tortricidae (Tho 1987, Natawiria 1990), and Noctuidae (Hedlin and Eungwijarnpanya
1984, Kamnerdratana et al. 1987, Hutacharern 1990) are common. Hymenoptera
is represented by Chalcidae (Kamnerdratana et al. 1987), Torymidae (Hedlin and
Eungwijarnpanya 1984), and Formicidae (Baksha and Islam 1990, Bandara 1990).
of all seed samples (San Valentin 1982). Viado (1979) observed scolytid seed borers
attacking mangrove species (Rhizoporaceae) in Negros Oriental.
Microflora group
In a related study on the pests and diseases of seeds and seedlings of forest
plantations in the Philippines, Quiniones (1983) reported that damping-off was the most
commonly observed disease which is caused by several species of fungi belonging to
the genera, namely: Phythium, Phytopthora, Fusarium, Rhizoctonia, and Sclerotium.
Seed collection
Seed collection was done in the months of June, July, and August 2003 when the
mature seeds of bungalon and api-api were available. Seed-bearing twigs using a pruning
shear were detached from standing trees. For the year 2003, 200 seeds of api-api from
Pagbilao, Quezon and 200 seeds of bungalon from Lian, Batangas were collected.
About 25 g of seed samples for each seed lot were weighed and placed inside
the plastic bag. The four empty aluminum containers were weighed individually and each
weight was recorded and designated as M1. Five grams of seed samples were then put in
each container and then both the sample and the container were weighed. The weight
was recorded as M2. The sample and the container were oven dried at 103 ± 2 oC in the
Seed Laboratory for 17 hours starting 4 PM to 9 AM the following day. The container and
the sample were again weighed after cooling for 20 minutes in the dessicator and the said
weights were recorded as M3. The MC was computed using the following formula:
M2 - M3
Percentage MC = X 100
M2 - M1
86 C. C. Marquez and V. O. Sinohin
Direct examination
Samples of 400 bungalon seeds and 400 api-api seeds were placed in plastic
trays and examined using binocular microscope to identify the presence of pathogen
or its fruiting structures like mycelium and spores. External evidence of insect damage
such as exit holes on seeds, webbings, and frass were also observed and recorded.
Blotter test
Blotter test was performed using the sample in the dry inspection test. Four
hundred seed samples at 50 seeds per replicate of each species of Avicennia were
placed equidistantly in plastic trays lined with three layers of paper towels moistened
with sterile distilled water.
The number of healthy germinated seeds using blotter test was counted and
percentage germination was determined using the following formula :
Number of seeds germinated
Percent germination = X 100
Total number of seeds sown
Seed health testing 87
Number of infested seeds
Percentage of infested seeds = X 100
Total number of seeds sown
Data analysis
Correlation and regression analyses were used to test the association of pest
damage on seed viability of Avicennia spp.
Moisture Content (MC) test did not show any significant difference between
the two species of Avicennia. Seeds of bungalon (Avicennia marina) and api-api (A.
officinalis) exhibited a high percentage MC of 61.5 and 64.56, respectively (Table 1).
These figures indicate a recalcitrant seed behavior of Avicennia spp.
Table1. Summary of seed health test showing percent MC, fungal infection,
infestation, and germination of A. marina and A. officinalis.
Fungal infection
Infestation
Table 2. Percentage frequency of fungal species isolated from the seeds of Avicennia spp.
Host Range. In Asia, host range includes Artocarpus spp. (Moraceae); breadfruit (A.
altilis), jackfruit (A. heterophyllus), chempedak (A. integer), and bitter gourd. Host
records from other families include Cucurbitaceae, Rutaceae, and Passifloraceae
(Carroll et al. 2004).
Host Range: The caterpillar of this species has been reported feeding on a variety of
plants belonging to the following families: Acanthaceae, Asteraceae, Primulaceae,
Lamiaceae, Ericaceae, and Hydrophyllaceae.
Diagnostic Characters. The head is small, greenish white with pale brown platelets.
T2, T3, and abdomen are mostly greenish white with white interrupted longitudinal
stripes. The larva is light green, long and skinny compared to other caterpillars (Fig. 2).
The adults are small with long and slender bodies. The wings split into two or three
feather-like divisions (Fig. 3) The forewings are divided into two while the hind wings
are divided into three (Stehr 1987).
Damage. A. officinalis is chiefly damaged by the larva that bores into its seed from
an egg laid on the seed coat. Upon gaining entry, the larva feeds internally on the
soft tissues of fully developed cotyledon leaving a considerable evidence of damage
in the form of partially devoured seeds. Conspicuous frass and webbings are also
deposited on the seed surface (Fig. 4). During heavy infestation, the larva of the insect
consumes the entire cotyledon of the seed causing gross destruction. The same feeding
damage was reported by Minchiton and Dalby-Ball (2001) in their investigation on
the frugivory by insects on propagules of A. marina. One of the dominant frugivores
they identified was also a plume moth (Cenoloba obliteralis) that attacked 80% of the
cotyledons of seedlings.
Seed health testing 91
Figure 2. Larva of plume moth. Note the small, greenish white head
of the larva and the damage it made on the seed.
Figure 3. The hind wing of adult plume moth. Note that it splits
into three feather-like divisions.
92 C. C. Marquez and V. O. Sinohin
Diagnostic characters. The adults are usually blacker than Sitophilus oryzae, with
fine microsculpture and are shinier. These are almost indistuinguishable from other
calandrinine beetles externally; thus, identification has to be done by examination
of the genitalia. They have the characteristic rostrum and elbowed antennae of the
family Curculionidae (Fig. 5). They also have circular, rather than oval punctures on
the prothorax (Fig. 6) (Booth et al. 1990).
Damage. A. marina seeds infested by larvae and adults showed extensive damage
consist of tunneling and exit holes with signs of frass around the eaten seeds.
Based on literatures, adult weevils usually lay their eggs on developing fruits
(Bonner et al. 1994). Upon hatching, the larvae grow to maturity within the developing
seed and then pupate. On emergence, the adults bite their way out, leaving round
exit holes. During severe infestation, 2-3 weevils can develop within a single seed
that is hollowed out by chewing larvae.
Seed health testing 93
Diagnostic characters. The adult of this noctuid moth is pale yellow in color with light
brown stripes horizontally inclined (Fig. 7).The forewings are narrower compared to
the hind wing which is slightly broader. The larvae of noctuidae are usually smooth
or with very little hairs, and moves in a geometrid or inch-worm fashion (http://www.
entomology.tfrec.wsu.edu/noctuid/id.html)
Damage. The caterpillar is the destructive stage that causes fruit and foliage damage.
In a related study, seed-feeding larva of other noctuid species was reported to be a
serious pest of Avicennia alba which can damage the fruit embryo and destroy up to
eight fruits before pupation takes place in the last one (htpp://mangrove.nus.edu.sg/
guidebook/text/2019.htm). Some reports, however, indicate that some adults feed on
nectar from flowers but many species will also feed on ripe or decaying fruit (http://
www.brisbane_noctuidae/index.htm/).
Economic importance. Some species in this group are serious pests of various crops
including A. alba.
Diagnostic characters. Tineid moths are small, yellowish moths whose larvae feed on
wool or fur. Generally, they have slender, elongated, fringed wings with a spread of
12 to 25 mm and dull mottled coloration. They have erect hairs on their heads and
long antennae. Most tineidae rest with wings raised tent-like over the body and the
body parallel with the substrate (Robinson and Nielsen 1993).
Seed germination. Table 1 indicates that Avicennia spp. exhibited low to moderate
germination rates of 30.0 and 48.0, respectively. Of the two species, A. marina had
a considerably higher germination rate than A. officinalis. This study indicates that
seeds of A. marina can germinate successfully despite substantial damage caused by
insects and fungal infection. This may be due in part to the preference of the insects
to feed on the soft tissues of the endosperm, thus, leaving the embryo undamaged. In
addition, it is interesting to note that Avicennia propagules have large cotyledons that,
accordingly, can lose a substantial amount of tissue and still be established as viable
seedlings (Sousa et al. 2003). In such cases, large cotyledons or endosperms provide
an effective mechanism for tolerating herbivore damage (Rosenthal and Kotaven
1994). Moreover, Avicennia seeds grow precociously. The seeds germinate rapidly
before they separate from the parent tree, thus, providing seed feeders and pathogens
a slim chance to injure the seeds and affect germination. Such rapid germination is
probably another defense mechanism of the species to reduce the duration of seed
exposure to seed predators (Daws et al. 2005). Furthermore, it was also reported
that Avicennia tissues contain iridoid glycosides (Fauvel et al. 1995) that serve as a
defense against attack of generalist plant feeders (Bowers 1992).
Correlation analysis. Results of correlation analysis using rate of fungal infection and
insect infestation on seed germination showed that no significant linear relationship
was detected between fungal infection and germination in both species of Avicennia.
Only a small amount of seed tissue was colonized by each fungus. Moreover, the
96 C. C. Marquez and V. O. Sinohin
fungi, particularly the saprophytic fungi like Aspergillus niger and Penicillium sp.
usually colonized only the seed coats while the embryo, which is the life of the plant
and the other internal parts of the seed remained undamaged.
The five seed-feeding insects that were identified include a fruit fly (B. umbrosa
Fabricious), a snout beetle (Coleoptera: Curculionidae), a plume moth (Stenoptilodes
sp.), a noctuid moth (Lepidoptera: Noctuidae) and tineid moth (Lepidoptera:
Tineidae). Based on the study, a curculionid infesting A.officinalis seemed to be the
most destructive species among the seed-invading organisms identified.
Using blotter test method, the species of fungi that were isolated include
Curvularia sp., Fusarium solani, and Aspergillus sp. in A. marina and Phomopsis
sp., Aspergillus niger, and Penicillium sp. in A. officinalis. Of the six species of fungi
isolated, Aspergillus niger had the highest frequency of occurrence.
Recommendations
The above study clearly demonstrated that seeds of Avicennia like any
other plant or forest trees species are prone to seed-invading organisms like insects
and fungi. The study also revealed that seed germination of Avicennia spp. was
considerably affected by the presence of seed-feeding insects. These findings provide
the evidence on the importance of seed health testing in Avicennia in detecting the
presence and even the level of fungal contamination and insect damage that cause a
marked reduction in seed germination.
• Seeds infected with storage and field fungi such as those belonging to the genera
of Aspergillus and Penicillium may be treated with contact fungicide such as
Dithane and Captan while seeds infected with pathogenic fungi such as Phomopsis
Curvularia and Fusarium may be treated with systemic fungicide like Benlate.
• Ground collected seeds that have higher incidence of fungal and insect damage
should not be used.
98 C. C. Marquez and V. O. Sinohin
Acknowledgement
This study was funded by DENR-ERDB and the Public Estate Authority (PEA).The
authors are grateful to the following individuals who deserve particular recognition: the
management staff of ERDB for administrative and logistic support; the Chief of CZFERD, Engr.
Santiago R. Baconguis, Lotic Section Chief, Dr. Carmelita I. Villamor and the CZFERD staff for
their encouragement and whole-hearted support; Mrs. Maria DP. Dayan for identifying the
fungi and allowing us to use the facilities in the Seed Laboratory; Dr. Jessamyn R. Adorada of
NCPC for kindly providing the identification of insect specimens; and Ms. Chita Dimaculangan
for her assistance in data gathering;
Literature Cited
Agmata, A.L. 1979. Seed-borne organisms in some forest tree seeds in the Philippines: a
preliminary survey. Sylvatrop, the Technical J. of Philipp. Ecos. and Nat. Res. 4(4):215-222.
Agrawal, R.L. 1980. Seed Technology. Oxford and IBH Publishing Co., New Delhi.
Akanbi, M. and Odeyinde. 1990. Entomology and Nigeria’s rain forest conservation strategy. In
C. Hutacharern et al. (Eds.) Proceedings of the IUFRO Workshop on Pests and Diseases of
Forest Plantations. Rapa Publication. pp. 67-69.
Baksha, M.W. and M.R. Islam. 1990. Summary of recent activities on forest insects in Bangladesh.
In C. Hutacharern et al. (Eds.) Proceedings of the IUFRO Workshop on Pests and Diseases of
Forest Plantations. Rapa Publication. p. 43.
Balciunas, J.K., D.W. Burrows and M.F. Purcell. 1994. Field and laboratory host ranges of the
Seed health testing 99
Australian weevil, Oxyops vitiosa, a potential biological control agent for the paperbark tree,
Melaleuca quinquenerva, Biological Control 4: 351-360.
Bandara, P.D. M.G.D. 1990. Insects and diseases of forest plantation in Sri Lanka. In Hutacharern
et al. (Eds.) Proceedings of the IUFRO Workshop on Pests and Diseases of Forest Plantations.
Rapa Publication. pp. 81-85.
Bonner, F.T., J.A. Vozzo, W.W. Elam and S.B. Land, Jr. Tree seed technology training Course.
Gen. Tech. Rep. SO-106.New Orleans, LA: U. S. Department of Agriculture, Forest Service,
Southern Forest Experiment Station: 98-102.
Bowers, M.D. 1992. Iridoid glycosides. In W.P. Sousa, P.G Kennedy and B.J. Mitchell. 2003.
Propagule size and predisposal damage by insects affects establishment and early growth of
mangrove seedlings. Oecologia 135: 564-575.
Carroll, L.E., A.L. Norrbom, M.J. Dallwitz and F.C. Thompson. 2004. Pest fruit flies of the world-
larvae. Version: 13th April 2005. Avail from: http: //delta-intkey.com.
Daws, M.I., N.C. Garwards and H.W. Pritchard. 2005. Traits of recalcitrant seeds in a semi-
deciduous tropical forest in Panama: Some ecological implications. Functional Ecology,
Vol.19, Issue No. 5. p. 874.
De Mesa, A. 1934. Forest host plants of injurious insects in the Philippines. Makiling Echo.
13: 245-50.
Fauvel, M.T., A. Bousquet-Melou, C. Maoulis, J. Gleye and S.R. Jensen.1995. Iridoid glucosides
from Avicennia graminans. Phytochemistry 38: 893-894.
Hardy, D.E. 1973. The fruit flies (Tephritidae-Diptera) of Thailand and bordering countries.
Pacific Insects Monograph, 31:1-353.
Hardy, D.E. 1982. The Dacini of Sulawesi (Diptera: Tephritidae). Treubia, 28: 173-241.
Hardy, D.E. 1983. The fruit flies of the genus Dacus Fabricius of Java, Sumatra and Lombok,
Indonesia (Dipter: Tephritidae). Treubia, 29:1-45.
Hedlin, A.F. and S. Eungwijarnpanya. 1984. Studies on seed insects of some forest trees.
Embryon. ASEAN-CANADA Forest Tree Seed Centre.
Hutacharern, C. 1990. Forest insect pests in Thailand. In C. Hutacharern et al. ( Eds. ) Proceedings
of the IUFRO Workshop on Pests and Diseases of Forest Plantations. Rapa Publication. pp.
75-80.
100 C. C. Marquez and V. O. Sinohin
Lamb, A.F.A. and O.O. Ntima. 1971. Terminalis ivorensis. Fast growing timber trees of the
lowland tropics. No. 5. Common. For. Inst. Oxford.
Lapis, E. 1984. Survey of insects associated with seed and essential oil tree species. FORI-
PCARRD Project (Unpub.)
Mehdi, F.S. and S.M. Saifullah. 1992. Mangrove fungi of Karachi, Pakistan. Journal of Islamic
Academy of Sciences 5: 1, 24-27.
Melana, E.E. 1991. Preliminary assessment of bungalon (Avicennia marina ( Forsk) Viech) as
mangrove reforestation species. Ecosystems Research Digest.1(1): 25-29.ERDS-DENR,
Region 7, Banilad, Mandaue City.
Militante, E.P. 1978. Identification, pathogenecity and control of fungi causing damping-off
disease of Benguet pine (P. kesiya Royle ex Gordon) seedlings under Philippine conditions.
MS Thesis. UPLB Graduate School, Los Banos.
Natawiria, D. 1990. Insect pests in plantation forests in Indonesia. In C. Hutacharern et al. (Eds.)
Proceedings of the IUFRO Workshop on pests and diseases of Forest Plantations. Rapa Pub.
p. 59.
Pacho, M.V. 1985. Survey of seed-borne fungi and effect of fungicide treatments on certain
Philippine forest tree seeds and selected samples from the DANIDA Forest Seed Center,
FORI. (Unpublished).
Robertson, A.I., R. Giddins and T.J. Smith. 1990. Seed predation by insects in tropical mangrove
forests: Extent and effects on seed viability and the growth of seedlings. Oecologia 83: 213-
219.
Robinson, G.S. and E.S. Nielsen. 1993. Tineid genera of Australia (Lepidoptera) Monographs on
Australian Lepidoptera, 2: i-xvi, 1-344, Figs. 1-733.
Rosenthal, J.P. and P.M. Kotanen. 1994. Terrestial plant tolerance to herbivory. In W.P. Sousa,
P.G. Kennedy and B.J. Mitchell. 2003. Propagule size and predispersal damage by insects
affects establishment and early growth of mangrove seedlings. Oecologia 135: 564-575
San Valentin, H.O. 1982. Survey and control of insects infesting the seeds of ipil-ipil. FORI, Los
Baños, Laguna (Unpublished Report).
Singh, P. 1990. Insect pest in plantations of native tree species in India. In Proceedings of the
IUFRO Workshop on Pests and Diseases of Forest Plantations. Rapa Pub. pp. 46-51.
Sinohin, V.O., D.C. Garcia and S.R. Baconguis. 1996. Manual on mangrove nursery establishment
and development. ERDB-DENR.19 pp.
Sousa, W.P., P.G. Kennedy and B.J. Mitchell. 2003. Propagule size and predispersal damage
by insects affects establishment and early growth of mangrove seedlings. Oecologia 135:
Seed health testing 101
564-575.
Stehr, F.W. 1987. Immature Insects. Kendal Hunt Publishing Company, Dubuque, Iowa 729 pp.
Suratmo, F.G. 1987. Current potentially dangerous forest pests in Indonesia. In Proceedings of
BIOTROP Symposium on Forest Pests and Diseases in Southeast Asia. BIOTROP Special
Publication No. 26. SEAMEO-BIOTROP, Bogor, Indonesia, pp. 91-95.
Tho, Y.P. 1987. Forest pests in Peninsular Malaysia. In Proceedings of BIOTROP Symposium on
Forests Pests and Diseases in Southeast Asia. BIOTROP Sp. Pub. No. 26, pp. 11-20.
Vagalo, M.R. Hollingsworth and F. Tsatsia. 1997. Fruit fly fauna in Solomon Islands. pp. 81-86 In:
Allwood, A.J. and R.A.I. Drew, Management of fruit flies in the Pacific. ACIAR Proceedings
No. 76, 267 pp.
Viado, G.B. 1979. Notes on insect pests of forest trees. Sylvatrop, The Technical J. of Philipp.
Ecos. and Nat. Res. 4(3): 183.
http://www.nhm.ac.uk/research curation/projects/tineidae/#what
http:www.geocities.com/Brisbane-moths/NOCTUIDAE.htm
http:www.canadianbiodiversity.mcgll.ca/English/species/insects/insectpages/Noctuidae.htm
102 C. C. Marquez and V. O. Sinohin
Sylvatrop, The Technical Journal of Philippine Ecosystems and Natural Resources 19 (1 & 2): 103 - 128
This thesis aims to: 1) assess the water quality of the Zwalm River
Basin in Belgium based on benthic macroinvertebrates, 2) apply the AQEM
assessment system on the Zwalm River Basin for calculating the newly
developed AQEM Ecological Quality Class (EQC) and compare their
results with the Belgian Biotic Index (BBI), Indice Biologique Globale
Normalise France (IBGN), Average Score Per Taxon (ASPT), Biological
Monitoring Working Party System (BMWP), diversity and evenness
indices, and 3) assess trends between the indices and physico-chemical
parameters and hydro-morphological characteristics.
The biological monitoring has also been used and established as an integral
part of the water quality monitoring (De Pauw and Hawkes 1993). In Flanders,
Belgium, one of the projects which aims to fully strengthen the biological monitoring
system is the AQEM Project otherwise known as the "Development and Testing of
an Integrated Assessment System for the Ecological Quality of Streams and Rivers
throughout Europe using Benthic Macroinvertebrates". It aims to develop a Europe-
wide system to assess the ecological quality of rivers using macroinvertebrates based
on the requirements of the European Union Water Framework Directive (EU WFD).
1. Assess the water quality of the Zwalm River Basin based on benthic macroinvertebrates.
Comparison of water quality indices
105
2. Apply the AQEM assessment system on the Zwalm River Basin for calculating newly
developed AQEM Ecological Quality Class (EQC).
3. Assess relationships among indices (ie., EQC, BBI, IBGN, ASPT, BMWP, diversity,
and evenness indices).
Review of Literature
environmental variations since sensitive life stages will respond quickly to stress. These
advantages are coupled with an ease in sampling by using inexpensive gear.
The EQC was derived from AQEM assessment system as a main scientific
achievement of the AQEM project which is under the Fifth Framework Programme of the
European Union. The AQEM assessment system is based on a "multimetric" procedure
(Fig.1). The development of an assessment system is an ambitious Europe-wide project
designed to put the EU WFD into practice. It involves the eight European countries
of Sweden, Germany, The Netherlands, Czech Republic, Austria, Italy, Portugal, and
Greece. Applying AQEM is very essential because the EU WFD legislates at a Europe-
wide level but no Europe-wide assessment system currently exists. This method is
not designed to replace or negate the existing assessment systems carried out by the
individual states but instead will be incorporated as an additional module (Buffagni et
al. 2001). Based on a macroinvertebrate taxa list obtained from the sampling stretch
using the European harmonized method, AQEM classifies a stream stretch into an EQC
presented as follows: 5-high, 4-good, 3-moderate, 2-poor, and 1-bad.
The calculation results are summarized into two separate sheets: metrics and
summary. The 'Metrics' table contains the results of all metrics calculated by the
program. The summary sheet which automatically appears when the 'Sample' score
window is opened contains the determined EQC and the results of those metrics used
to calculate it.
Assessment
Country Reference Identification Scoring Description Remarks
System
Biological United Armitage et Family ASPT < 25 The ASPT score For the unpolluted
Monitoring Kingdom, al. Family = very poor generally rises streams, the index
Working Ireland, 1983; Wright (red); 26-50 = with improving must be evaluated
Party System Sweden, et al. 1984. poor (orange); water quality relative to type-
- Average USA 51-100 = and structural specific because
Score Per moderate diversity. scores vary
Taxon (yellow); 101- for unpolluted
(BMWP- 150 = good streams of
ASPT) (green); >150 different typology.
= very good
(blue)
Belgian Biotic Belgium, De Pauw & Genus 1-2 = very Increasing The results are
Index (BBI) Portugal, Vanhooren bad quality pollution will sufficient for
Spain, 1983; De (red); 3-4 = result in a loss different stream
Luxembourg, Pauw et al. bad quality of diversity and channels but may
Greece 1992 (orange); 5-6 a progressive fail in deep waters.
= moderate elimination of
quality certain pollution-
(yellow); 7-8 sensitive groups.
= good quality
(green); 9-10
= very good
quality (blue)
L. T. Aragoncillo
Continuation...
BWMP Score UK, Sweden, Armitage Family No defined Increasing Used in UK for
Ireland et al. 1983; scoring system. pollution will routine
Wright et al. result in a loss investigation of
1984. of diversity and organic stream
a progressive pollution.
elimination of
certain pollution-
sensitive groups.
Comparison of water quality indices
Diversity Worldwide Armitage DISW >3 is Diversity index Most suited for
Index et al. 1983; considered increases with assessing impact of
Wright et al. high quality. the number of organic pollution,
1984. species in the general gradation
community. of streams.
The basin is mainly polluted by untreated urban wastewater and diffused pollution
originating from agricultural activities. In the months of August and September 2000,
60 sites of the Zwalm sub-basin (part of the Upper-Scheldt Basin) in Flanders, Belgium
were investigated (Fig. 3).
In shallow rivers, the handnet method was used. The macroinvertebrates were
collected by means of kick sampling with a standard handnet consisting of a metal
frame holding a conical net (mesh-size 500µm) (IBN 1984). The sampling method is
Comparison of water quality indices
Figure 3. Zwalm River Basin is located in the Upper-Scheldt Basin in Flanders, Belgium (Adriaenssens 2002).
111
112 L. T. Aragoncillo
based on a multi-habitat design, where major habitats are sampled according to their
proportional distribution within a sampling reach and consisted of 10 minutes sampling
in a 10 m reach of the watercourse. In deep rivers and canals, artificial substrates were
used. Artificial substrates are made of plastic netting with pieces of bricks which are
exposed in the field for about four weeks (De Pauw & Vanhooren 1983). Collection
of substrate was undertaken followed by proper washing, filtering using handnet,
collecting the filtered samples before properly preserving in a bucket using formalin,
and bringing the samples to the laboratory for further biological analysis.
The coarse debris was removed and the organisms retained on each sieve
are transferred to white plastic sorting trays (30x50 cm). The bottom of the sorting
tray was divided into squares to facilitate the systematic examination of the material
collected. The organisms were sorted and transferred to small flasks and were roughly
grouped according to major taxonomic groups being preserved in denatured 70%
alcohol (De Pauw & Vanhooren 1983). After separation, marcroinvertebrates were
identified under a stereoscopic dissection microscope (10 to 50 times magnification).
The purpose of identification is to determine the number of systematic units present
in the sample (diversity) and the presence of the most sensitive faunistic groups.
Consequently, the identification for the systematic units was performed only up to a
practical level (family and genus).
Physico-chemical parameters
The AQEM software is only a calculation program and is not designed for
storing data. It is based on Excel as common and comparatively compatible computing
Comparison of water quality indices
113
system, to which most databases are able to export data sheets. The AQEM software
is capable of importing a taxa list and exporting results in either Excel (*.xls) or ASCII
file format. Preparing data sets for import into the AQEM software must be done
using a different program such as Excel or a text editor. The following steps were
undertaken for the proper data processing:
Based on the AQEM assessment system, the EQC was calculated for all
sampling sites using the appropriate stream type. Stream types namely small Dutch
hill streams and small Dutch lowland streams were chosen for calculating the EQC
since these stream types are mostly related to the Zwalm River Basin in terms of size,
altitude, ecoregion, and geology. The system also calculated other chosen indices like
the BBI, IBGN, ASPT, BMWP, DISW and Evenness using the chosen stream types.
The classes’ ranges of the different indices (BBI, IBGN, and ASPT) and the newly
developed EQC could only be possible for these selected indices since these are the
ones with scoring system (Table 2).
The correlation analysis was performed for the datasets with the use of
S-Plus professional edition version 6.1.2 release 1 (Lucent Technology, Inc. 2002).
Correlation analysis is a tool to determine whether two ranges of data move together,
Table 2. The definition of the classes' range of the different indices and the EQC.
Classes’ Range
1 2 3 4 5
EQC Bad Poor Moderate Good High
BBI Very bad Bad Moderate Good Very Good
IBGN Very bad Bad Moderate Good Excellent
ASPT Very bad Poor Moderate Good Very Good
114 L. T. Aragoncillo
whether large values of one set are associated with large values of the other (positive
correlation) and small values of one set are associated with large values of the other
(negative correlation) or whether values in both sets are unrelated (correlation near
zero). The correlation coefficient formula (r) is as follows:
Note:
n r = correlation coefficient
Σ ( xi − x)( y i − y ) n =
x, y =
number of variables
variables
r= i =1
s’ = modified standard deviation
(n − 1) s ' x s ' y x = mean of x variable
y = mean of y variable
Comparison of the results between the indices (BBI, ASPT, IBGN, and AQEM
EQC) with specified class ranges are shown in Figure 4. Results showed that the
AQEM-EQC for both stream types and the BBI showed that most of the sampling sites
in the Zwalm River Basin were moderately polluted. On the other hand, the ASPT
and IBGN showed mostly very bad/very poor quality. Of all the indices, only the BBI
recorded some sites into the quality class "very good".
There are no score systems for the BMWP, DISW, and Evenness because
these indices need to be compared to the reference condition for each stream type.
The BMWP scores ranged from 6-101 but because of the lack of a scoring system, the
index could not be evaluated. The recorded values for the DISW ranged from 0.088-
2.020. Studies showed that surface waters with DISW >3 were considered to be of
high quality (Shannon & Weaver 1949). Evenness registered values were 0.04-0.861.
The results obtained from the correlation analysis of the observed water
quality of the Zwalm River based on different indices are illustrated in Figure 5.
The results further revealed that the AQEM-EQC for both stream types have low
correlations with the other indices. Although low correlations have been attained, the
Comparison of water quality indices
115
Figure 4. Comparison of the results between the indices with specified class ranges.
LEGEND:
Physico-chemical parameters
At all measuring points in the Zwalm River Basin, the major physico-
chemical parameters analyzed were evaluated based on the Belgian Water Quality
(WQ) Norms (Besluit Vlaamse Exekutieve 1987) and the correlation analyses among
the different physico-chemical parameters (Fig. 6 and 7).
Figure 6a. D.O. (mg/L) assessment based on Belgian Water Quality norms.
118 L. T. Aragoncillo
Figure 6b. C.O.D (mg/L) assessment based on Belgian Water Quality norms.
Figure 6c. NO3 (mgN/L) assessment based on Belgian Water Quality norms.
Comparison of water quality indices
119
Figure 6d. NH4+ (mgN/L) assessment based on Belgian Water Quality norms.
Figure 6e. Total N (mgN/L) assessment based on Belgian Water Quality norms.
120 L. T. Aragoncillo
Figure 6f. PO43- and Total P+ (mgP/L) assessment based on Belgian Water Quality norms.
Figure 6g. S.S. (mg/L) assessment based on Belgian Water Quality norms.
Comparison of water quality indices
121
Sewer systems from the households undergo anaerobic process due to the
absence of oxygen, thus, enhancing NH4+ concentration in the Zwalm River Basin. It
was very evident in the sampling sites (30 and 40) where DO and NO3- concentrations
were at the lowest and NH4+ recorded the highest (Fig. 6a, c, and d). This was also
shown in the calculated positive correlation between DO and NO3- and negative
correlations between NH4+ with DO and NO3- (Fig. 7). This was also true for PO4 3-
and TotalP data sets. At sampling sites 30 & 40, the recorded value is 4.3 mgP/L in both
sites (Fig. 6f). Studies also stated that erosion from agricultural areas will result to high
suspended solids (SS), which is a significant source of high phosphorus concentrations
in the river water. This was depicted in the results where PO43- and TotalP are at the
highest and SS were also high (Fig. 6f and g). Positive correlations were also shown
between these physico-chemical parameters (Fig. 7).
Out of the 60 sampling sites, there were only four sites that exceeded 1,000
µS/cm Belgian WQ norm for conductivity. The conductivity of most freshwaters
ranged from 10-1,000 µS/cm but may have exceeded 1,000 µS/cm especially in
those receiving large quantities of agricultural run-off, which was evident in the four
mentioned sampling sites in the Zwalm River Basin.
Results showed that generally all the indices illustrated very low correlations
with all the physico-chemical parameters (Fig. 8). Thus, it can be deduced from the
results that there was no clear relationship between the indices and the physico-
chemical parameters. The BBI, on the other hand, had better correlations with the
physico-chemical parameters (Fig. 8). The positive correlation with DO and NO3-
concentrations means that at high DO and NO3- concentrations, high BBI values
can also be observed. Negative correlations were depicted between BBI with COD,
NH4+, Total N, PO43-, and Total P. Thus, at sampling sites with higher values of these
physico-chemical parameters and influenced by organic pollution from agricultural
and domestic activities, tolerant species can be found as depicted from BBI values.
LEGEND:
Figure 7. Correlation analysis of the different physico-chemical parameters in the Zwalm river basin.
L. T. Aragoncillo
Comparison of water quality indices
Figure 8. Correlation analyses between indices and physico-chemical parameters a) Cond by BBI, b) TotalP by BBI,
c) NH4 by BBI, d) DO by BBI, e) Tempo by BBI, f) SS by BBI, g) TotalN by BBI, h) COD by BBI, i) pH by
BBI, j) PO4 by BBI, and k) NO3 by BBI.
123
124 L. T. Aragoncillo
Based on the results, the concept of RCC cannot be proven through the data sets in
the Zwalm River Basin because of the very low correlations and insufficient data available.
One of the problems encountered when analyzing the RCC of Zwalm River Basin was
that it did not take into account the strong influence of human impact on the continuum.
The original testing of the RCC was focused on natural, undisturbed systems, which was
unfortunately not the case of the Zwalm River Basin. Thus, the results presented may not
be sufficient to conclude the theory behind the RCC. When one wants to prove the proper
adaptation of the BBI and EQC in order to make them type-specific, this experiment has to
be undertaken in a more natural and pristine river basin.
This study presents the results of the application of the newly developed
AQEM assessment system to the Zwalm River Basin. Specifically, the study identified
and assessed the trends and relationship of the biological parameters (through indices
measurements via the AQEM assessment system) with the physico-chemical and
hydro-morphological parameters. Although low correlations were attained, the results
further revealed that there is a common pattern showing the relationship between the
indices and the physico-chemical parameters, specifically NH4+, DO, COD, total P,
PO43-, total N, and conductivity.
1. The data set did not include a lot of sites with a diverse biological community and
good water quality which could test the results in the reference conditions.
2. The response of the indices to pollution sources did not show any linear relationship,
therefore it might be necessary to test non-linear relationship (e.g., unimodal or
other statistical analysis).
Comparison of water quality indices
125
3. Some applied indices are too specific for the region for which they are developed,
thus, might not be applicable to the Zwalm River Basin.
4. The study is only limited to the application of the two stream types: Small Dutch
Hill Streams and Small Dutch Lowland Streams.
5. The level of identification (genus and family level) is not refined enough. Slight
differences in organic pollution and the impact of stream morphology degradation can
only be detected if species level is applied. Therefore, further studies should focus on
a more refined typology to apply the idea of the stressor-specific assessment which
will further identify the causes or impacts of different stressors on the community.
1. Pilot applicability in the Laguna de Bay Basin because this can easily be tied-up
with existing research agenda of LLDA.
3. Laguna de Bay Watershed possesses numerous river systems which could represent
diverse reference conditions, which are still natural and undisturbed. This could
serve as future study area to support the theory behind the RCC.
4. More replicate sites and samples should be established in order to improve statistical
analysis.
Literature Cited
AQEM Consortium. 2002. Manual for the application of the AQEM system: A comprehensive
method to assess European streams using benthic macroinvertebrates, developed for the
purposed of the Water Framework Directive. Version 1.0.
Armitage, P.D., D. Moss, J.F. Wright & M.T. Furse. 1983. The performance of a new biological
water quality score system based on macroinvertebrates over a wide range of unpolluted
running-water sites. Water Res. 17, 333-347.
Buffagani, A., J.L. Kemp, S. Erba, C. Belfiore, D. Hering, and O. Moog. 2001. A Europe-wide
system for assessing the quality of rivers using macroinvertebrates : The AQEM Project
and its importance for Southern Europe (with emphasis on Italy). Journal of Limnology. 60
(suppl. 1) 39-48.
Cairns, J. and Van der Schalie, W.H. 1980. Biological Monitoring: Part I – Early warning
Comparison of water quality indices
127
De Pauw, N. and H.A. Hawkes. 1983. Biological monitoring of river water quality. In River
water quality monitoring and control. W.J. Walley and S. Judd (Eds). Published by Aston
University, UK.
De Pauw, N. and Vanhooren, G. 1983. Method for biological quality assessment of water
course in Belgium. Hyrdobiolgia 100: 153-168.
European Union – Directive of the European parliament and of the council 2000/60/EC,
Establishing a framework for community action in the field of water policy.
Goethals, P. and De Pauw, N. 2001. Development of a concept for integrated ecological river
assessment in Flanders, Belgium. Journal of Limnology, 60, 7-16.
Hawkes, H.A. 1997. Origin and development of the Biological Monitoring Working Party
128 L. T. Aragoncillo
Institut Belge de Normanlisation. 1984. Qualité biologique des cours d’eau: détermination
de l’indice biotique se basant sur les macro-invertbrates aquatiques, NBN T92-402. IBN.
Karr, J.R. 1981. Assessment of biotic integrity using fish communities. Fisheries, 6: 21-27.
Lucent Technology, Inc. 2002. S-Plus Professional edition version 6.1.2 release 1.
Metcalfe, J.L. 1989. Biological water quality assessment of running waters based on
macroinvertebrates communities: History and present status in Europe. Environmental
Pollution 60:139.
Rosenberg, D.M. and Resh, V.H. 1993. Introduction to freshwater biomonitoring and benthic
macroinvertebrates. In freshwater biomonitoring and benthic macroinvertebrates D.M.
Rosenberg and V.H. Resh (Eds.) Chapman and Hall, New York.
Shannon, C.E. and W. Weaver. 1949. The mathematical theory of communication. University
of Illinois Press. Urbana, Illinois.
Sladecek, V., H.A. Hawkes, J.S. Alabaster, I. Daubner, I. Nötlich, J.F.D. Solbé, and D. Uhlmanh.
1982. Biological examinations. In Examination of water pollution control.
United States Environmental Protection Agency (US EPA). 1983. Results of the nationwide
urban runoff program. Vol. 1. Final Report. Office of Water, US EPA. Washington, DC.
US EPA. 1998. Stream corridor restoration: Principles, processes, and practices. Office of
Water, Washington, DC.
Vanhooren. 1989. Comparison of two biological index systems for water quality assessment
in Belgium. Comptes-rendus du Symposium Invertébrés de Belgique/ Verhand. Symp.
‘Invertebraten van Belgie. p. 429-435.
Vannote, R.L., Minshall, G. Wayne, K.W. Cummins, J.R. Sedell, and C.E. Cushing. 1980.The
River Continuum Concept, Canadian Journal of Fisheries and Aquatic Sciences.
Wiederholm, T. 1980. Use of benthos in lake monitoring. Journal of the Water Pollution
Federation, 52:537-547.
Whitton, B.A. 1979. Algae and higher plants as indicators of river pollution. In Biological
Indicators of Water. A. James and L. Evison (Eds.). John Wiley Chichester.
Wright, J.F., P.D. Armitage, and M.T. Furse. 1984. A preliminary classification of running water
sites in Great Britain based on macroinvertebrate species and the prediction of community
type using environmental data. Freshwater Biology 14:221-256.
Reviewers for this issue...
4. Seed health testing of Bungalon (Avicennia marina) and Api-Api (A. officinalis) by
Cynthia C. Marquez and Veronica O. Sinohin
Dr. Honorato G. Palis
Mr. Carlo C. Custodio
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