Professional Documents
Culture Documents
Effectsofhabitatfactors BlackShama ALS ISI 2015
Effectsofhabitatfactors BlackShama ALS ISI 2015
net/publication/295584340
CITATIONS READS
0 614
1 author:
Archiebald Baltazar
Cebu Technological University
18 PUBLICATIONS 30 CITATIONS
SEE PROFILE
All content following this page was uploaded by Archiebald Baltazar on 30 June 2020.
LIFE
SCIENCES
The Asian International
Journal of Life Sciences
Beyond Excellence ©
CONTENTS
469 A new distribution record of Hoya espaldoniana
Kloppenburg, Siar & Cajano (Section Acanthostemma:
Apocynaceae) A.S. Hadsall, M.A.O. Cajano,
I.A.F. Lambio & M. Alejado
477 Relationship between above- and below-ground
biomass for 18-year-old Abies holophylla under
different stand conditions H.-H. Lee & D.-H. Lee
493 The Philippine genus Stilbotes Stal and a new tribe
of Asopinae (Hemiptera: Pentatomidae) V.P. Gapud
499 Competitive ability of weedy rice against cultivated
rice in the Philippines E.C.Martin & I.R. Tanzo
507 Formulation of an environment and social impact
assessment tool for small scale economic activities in
coastal areas in the Philippines C.A. Cabrido, Jr.
537 Morphological variations of the white goby (Glossogo-
bius giuris Hamilton 1822, Teleostei: Gobiidae) in three
lakes of Southern Luzon, Philippines J.G. Campang &
P.P. Ocampo
Cont. on Next Page
Beyond Excellence©
81 Governor F.T. San Luis Avenue, Masaya, Bay 4033, Laguna, Philippines
Celfone nos. (063) (049) 0915-360-4660; 0921-374-9752; 0916-526-0164
e-mails: asialifesciences@yahoo.com wsmgruezo@gmail.com
http://journals.uplb.edu.ph/index.php/ALS
©Rushing Water Publishers Ltd., Philippines 2015
Point count method was used to determine the number of encounter or contact with
Copsychus cebuensis Steere (black shama) while microhabitat factors were determined using
GIS and other appropriate instruments and by calculation. Results suggest that elevation,
slope, shrub cover and tree density had negative effects on C. cebuensis distribution. This
means that the higher the values of these variables the lower the distribution of the target
species, C. cebuensis. As regard to exposure, north-facing slope had positive effect on
C. cebuensis distribution which means higher distribution, while west-facing slope had
negative effect. While distance from point-count station to intermittent stream or valley
bottom and canopy cover had positive effects which means that the nearer the point-count
stations to the valley bottom and the higher the value of canopy cover, the higher is the
C. cebuensis distribution. The various effects of microhabitat factors on the distribution
of the target species could be used as benchmark in predicting the habitat quality for
C. cebuensis. Hence, this could be utilized as an aid in making decision for further
conservation and management planning for the target species.
INTRODUCTION
Generally, the survival of many species of birds’ is relatively dependent on
the fluctuating environmental variables such as microhabitat and microclimate
(Rosli et al. 2012). However, these responses may vary with species physiological
tolerance, and most especially to nestlings (Hayworth & Weathers 1984, Burton
1995, Thomas et al. 2001, Harrison et al. 2003, Huntley et al. 2006, Hitch & Leberg
2007, Devictor et al. 2008, Virkkala et al. 2008, Rosli et al. 2012). In reality, species
that need forest interior may avoid edges due to changes in microclimate, vegetation
structure or high density predators or blood parasites (Yahner & Scott 1998; Malcom
1994, Marini et al. 1995, Stephens et al. 2003).
Black shama (Copsychus cebuensis Steere) is locally known as ‘siloy’ and is
endemic to Cebu Island, Philippines. A sedentary, non-migratory, and insectivorous
bird species that feeds on insects normally black beetles (Kennedy et al. 2000). This
bird species belongs to the order Passeriformis and Muscicapidae family which
inhabits primary forest, in the dense undergrowth of secondary habitats - usually
within a few meters from the ground where it is secretive, more often heard than
seen, in bamboo grooves, thickets and/or along steep ravines―particularly beside
ridge-top and valley-bottoms with a high percentage of canopy cover (Kennedy et
al. 2000, Birdlife International 2012). It breeds from February up to September.
According to the International Union for the Conservation of Nature (IUCN)
Red List of Threatened Species in 2012, this species qualifies as endangered as it
has a very small range and population, both of which are continuously declining
(Birdlife International 2012). Additionally, it suffers severe fragmentation owing
to extreme pressure on the few remaining, already highly degraded, tracts of
forest in Cebu Province that still support subpopulations (Birdlife International
2012). Likewise, biodiversity in Argao watershed is pervasively threatened from
degradation posed by human activities including settlement, land use conversion,
shifting cultivation, illegal cutting of trees for house construction, firewood
gathering and habitat clearance for mining. Consequently, these disturbances may
eventually affect the microclimate and microhabitat factors in the watershed area
and ultimately the present subpopulations of C. cebuensis.
A number of insectivorous species of forest birds are adapted to changes in
microclimate and microhabitat factors (Arriaga-Weiss et al. 2008). In the study of
Varesteh et al. (2010) found out that the distribution of some under storey birds
species are also correlated with canopy cover, number of trees and ground cover
as the consequence of forest edge and gaps. However, avifaunal species may
respond to one or a combination of these changes in the landscapes as a result of
various mechanisms of may be biological origin (Robinson et al. 1995). Studying
bird occurrences, densities and/or populations may therefore give a distinct result
because of environmental and habitat changes over the forest in a long time (Rosli
et al. 2012).
Zakaria et al. (2009) in their study on insectivorous birds and environmental
factors across an edge-interior gradient in tropical rainforest of Malaysia found out
that arboreal foliage gleaning insectivores were positively correlated with ground
cover, light intensity, shrub cover and percent of shrub cover. While terrestrial
insectivores, were sensitive to the forest edge and could indicate the quality of
forest interior habitat associated with high humidity, dense canopy cover and deep
litter depth. Rosli et al. (2012) studied the response of upper storey birds to the
environmental variables at different distances from the edge of an isolated forest
reserve in Malaysia and found out that the responds and the environmental variables
were significantly correlated.
Here in the Philippines, particularly at Subic Bay Forest Reserve (SBFR) the
effects of anthropogenic land use on the natural habitat have been studied and found
out that forest bird species are positively correlated with vegetation variables such
as canopy cover, tree density, height to inversion and ground cover (Posa & Sodhi
2006). Furthermore, the results also show that majority of the bird contacts are
sensitive to canopy loss. It requires at least a canopy cover of 60% or higher in
order to maintain at least good environmental condition for the birds which is in
conformity with the finding of this present study. A large proportion of endemics
here in the Philippines from both groups are dependent on forested habitats
(Dickinson et al. 1991, Settele 1993). Lastly, habitat and environmental quality
changes may also affect the population growth rate and the equilibrium population
size of plants and wildlife (Saunders et al. 1995).
Hence, this present study was the first attempt to assess the responds of
C. cebuensis in terms of its spatial distribution to some microclimate and microhabitat
variables or factors on the selected forest patches within Argao watershed.
erosion while the remaining three are non-resistant. The soil is generally clayey
to loamy in texture specifically the soil type in the area is consist of Mantalongon
clay loam which occupies 90% of the total study area and 10% falls under lugo
series which were derived from weathered limestone rocks and from calcareous and
sandstone in the bottom lands. the soil ph ranges from 6.5 to 8.2.
The study site falls under climate type III where rainfall distribution is not
pronounced but usually the onset of rainy season falls on the months of May until
November where at this month considered the wettest while dry season starts early
December until April where the driest is usually experience during the month of
March.
Figure 1. The location of the study site - Argao Watershed Reserve (with maps of
Cebu Province and Philippines, inset).
Argao watershed has two different types of forest cover, the naturally grown
trees which are indigenous or native species, and the man-made forest which are the
plantation, previously managed under Southern Cebu Reforestation Development
Project (SCRDP) in the early 1970’s. Some remnants of natural forest fragments
are found at the peak of Mt. Lantoy and at the slopes of Argao River. Isolated forest
patches are still present in barangays Canbantug, Panadtaran, Usmad, Tabayag,
Conalum and Cansuje. Mother trees of Ipil [Instia bijuga (Colebr.) Kuntze] and
Molave (Vitex parviflora Juss.) can also be found in these areas. Natural vegetation
and plantation forests comprise 29% (1,119.54 ha) of the watershed area (Jakosalem
& Paguntalan 2007).
Data collection technique for population counts of Copsychus cebuensis. This
study adopted the point count survey method following Expedition Field Techniques:
Bird Surveys by Bibby et al. (2000). A total of 130 circular point-count stations with
20 m radius had been established within the four sampling sites covering natural
and man-made forests. Of the total, 26 plots in Mt. Lantoy (Brgy. Tabayag), 23 in
Brgy. Canbantug, 38 in Brgy. Usmad and 43 plots in Brgy. Cansuje (Figure 2).
Figure 2. Plotted coordinates for the 130 point-count sampling stations within the
four sampling sites in Argao Watershed Reserve, Cebu, Philippines.
About 10 minutes were allocated for observation in each station. All target
species seen or heard around the plot within the fixed radial distance of 20 m were
recorded. The variables such as number of contacts or encounters with the target
species, start time, height of contact and the exact time when the contact happened
were recorded. The conduct of the survey was usually done 30 min before sunrise
until 1000 hr as birds were active during this time and late in the afternoon until
sunset or 1730 hr (Bibby et al. 2000). The survey was only undertaken during
days with fair weather or sunny. No survey was made during rainy days since bird
activities were suppressed during these days.
Data collection technique for microhabitat variables. The microhabitat variables
were gathered directly or indirectly from the field during which the point-count
sampling was conducted. These variables were broadly categorized into the
following: (a) physical and (b) vegetation features variables, respectively. Physical
variables included elevation, slope, exposure and distance to the nearest available
intermittent stream or valley bottom. Elevation and slope were measured directly on
field using GPS; exposure was obtained with the use of a compass while distances
of sampling plots to the nearest available intermittent stream or valley bottom were
determined indirectly by calculation using GIS (nearest neighbor distance analysis).
Canopy cover was measured directly in the field using Densiometer instrument,
while shrub cover and tree density were determined through direct ocular estimate
within the field and indirectly through computation using an equation by Bibby et
al. (2000) as follows:
Calculation of the density of trees around the point:
Distribution of Copsychus cebuensis with respect to slope. Figure 4 shows that the
highest number of contacts was found at the slope range of 31-45% while the lowest
was at slope range of 106-120%. In this variable, the same pattern of observation
was obtained as that of the effect of elevation with the number of contacts of the
target species generally decreases with increasing slope range.
lowest was at the western exposure. This could be attributed to the amount of light
or solar radiation received by areas of varying exposure.
In a separate study of Carrascal and Diaz (2006) found out that the most
essential habitat structure variables related to bird distribution were the density
of young and mature oaks: a thick undergrowth of thin oaks negatively influenced
total bird abundance and species richness. The impact of this variable towards the
distribution of the target species in the present study appeared to be that there is
an optimum amount of shrub cover that they thrived more favorably and beyond
which the distribution seemed to decrease. Hence, the role of trees and shrubs on
the distribution of the target species seemed to be complementary.
Distribution of Copsychus cebuensis as influenced tree density. Figure 9 shows
that the highest no. of contacts was at the range of 281-320 trees/ha, while the lowest
was within the range of 121-160 trees/ha. The same trend had been observed with
that of the effect of shrub cover in terms of the optimum amount of tree density
needed for the target species to thrive successfully in a particular microhabitat
condition. Once this range of tree density is overshoot, it is expected that the number
of contacts with the target species declines.
ACKNOWLEDGMENTS
This study received financial support primarily from the Department of Science and
Technology, Science Education Institute (DOST-SEI) under the Accelerated Science and
Technology Human Resource Development Program (ASTHRDP), Philippine Council
for Aquatic, Agriculture, Forestry and Natural Resources Research and Development
(PCAARRD) and the National Research Council of the Philippines (NRCP) for which the
author is very grateful.
LITERATURE CITED
Arriaga-Weiss, S.L., S. Calme and C. Kampichler. 2008. Bird communities in
rainforest fragments: Guild responses to habitat variables in Tabasco, Mexico. Biological
Consevation 17: 173-190.
Bibby, C., M. Jones and S. Marsden. 2000. Expedition Field Techniques: Bird Surveys.
Birdlife International, Cambridge, UK.
Bird Life International. 2012. Species Factsheet: Copsychus cebuensis. Available from
http://www.birdlife.org/.
Burton, J.F. 1995. Birds and Climate Change. Christopher Helm-A & C Black, London, UK.
Carracal, L.M. and L. Diaz. 2006. Winter bird distribution in abiotic and habitat struc-
tural gradients: A case study with Mediterranean montane oakwoods. Ecology Science
13(1): 100-110.
Cintra, R. and L.N. Naka. 2012. Spatial variation in bird community composition in
relation to topographic gradient and forest heterogeneity in a Central Amazonian
rainforest. International Journal of Ecology volume 2012, 25 p. doi10.1155/2012/435671.
Dickenson, E.C., R.C. Kennedy and K.C. Parkes. 1991. The Birds of the Philippines: An
Annotated Checklist. British Ornithologist’s Union, United Kingdom.
Farina, A. 1997. Landscape structure and breeding bird distribution in a sub Mediterranean
agro-ecosystem. Landscape Ecology 12(6): 365-378.
Huntley, B.Y., C. Collingham, R.E. Green, G.M. Hilton, C. Rahbek and S.G. Willis. 2006.
Potential impacts of climatic change upon geographical distributions of birds. Ibis
148: 8-28.
International Union for the Conservation of Nature (IUCN). 2012. Red List of Threatened
Species, Glans, Switzerland.
Jakosalem, P.G., L.M.J. Paguntalan and O.B. Orlanes. 2005. Distribution and habitat
requirements of the black shama Copsychus cebuensis (Muscicapidae). Forktail 22: 56-62.
Joshi, K., K.D. Bhatt and A. Thapliyal. 2012. Avian diversity and its association with veg-
etation structure in different elevational zones of Nainital district (Western Himalayan)
of Uttarakhand. International Journal of Biodiversity Conservation 4(11): 364-376. doi:
10.5897/IJBC11.243.
Kennedy, R.S., P.C. Gonzales, C. Pedro, E.C. Dickinson, H.C. Miranda and T.H. Fisher.
2000. A Guide to the Birds of the Philippines, 1st edition, Oxford University Press, New
York, NY, USA,
Leikola, N. and M. Lueto, 2008. Projected large-scale range reductions of northern-boreal
land bird species due to climate change. Biological Conservation 141(1): 343-1353.
Malcom, J.R. 2012. Egde effects in Central Amazonian forest fragments. Ecology
75: 2438-2445. Conservation [cited 2012 Aug] 4(11): 364-376, Available online at http://
www.academicjournals.org/IJBC.
Marini, M.A., S.K. Robinson and E.K. Heske. 1995. Edge effects on nest predation in the
Shawnee National Forest, southern Illinois. Biological Conservation 74: 203-213.
Moradi, H.V., M. Zakaria, A.B. Mohd and E. Yusof. 2009. Insectivorous birds and
environmental factors across an edge-interior gradient in tropical rainforest of Malaysia.
International Journal of Zoological Research 5(1): 27-41.
Pagaduan, D.C. and L.E. Afuang. 2012. Understorey bird species diversity along eleva-
tional gradients on the northeastern slope of Mt. Makiling, Luzon, Philippines. Asia Life
Sciences 21(2): 585-607.
Posa, M.R.C. and N.S. Sodhi. 2006. Effects of anthropogenic land use on forest birds and
butterflies in Subic Bay, Philippines. Biological Conservation 129: 256-270. Available
from www. sciencedirect.com.
Robinson, S.K., F.R. Thompsom, T.M. Donovan, D.R. Whitefield and J. Faabog. 1995.
Regional forest fragmentation and the nesting success of migratory bird. Conservation
Biology 14: 54-56.
Rosli, Z., M. Zakaria, A. Mohd, A. Yusuf, G. James and A. Khairulmazmi. 2012. Response
of upper storey birds to the environmental variables at different distances from the edge of
an isolated forest reserve in Malaysia. Asia Life Sciences 21(1): 65-84.
Saunders, D.A., R.J. Hobbs and C.R. Margules. 1995. Biological consequences of eco-
system fragmentation: A review. In: Ehfrenfeld, D. (Ed.). The Landscape Perspective.
Conservation Biology, 190 p.
Setelle, J. 1993. Lepidopterodical research in the Philippines-A short survey. Nachrichten
des entomologechen des entomoligis chen Vereins Apollo Supplement 12: 12-24.
Stephens, S.E., D.N. Koons, J.J. Rotella and D.W. Wielley. 2003. Effects of habitat
fragmentation on avian nesting success: A review of the evidence at multiple spatial scales.
Biological Conservation 115: 101-110.
Thomas, D.W., J. Blondel, P. Perret, M.M. Lambrechts and J.R. Speakman. 2001.
Energetic and fitness costs of mismatching resource supply and demand in seasonally
breeding birds. Science 291: 2598-2600.
Varesteh, H.M., M. Zakaria, A. Mohd and E. Yusofi. 2010. Insectivorous birds and
environmental factors across an edge-interior gradient in tropical rainforest of Malaysia.
International Zoological Research 6: 131-145.
Virkkala, R., R.K. Heikkinen, N. Leikola and M. Lueto. 2008. Projected large-scale
range reductions of northern-boreal land bird species due to climate change. Biological
Conservation 141: 1343-1353.
Whittingham, M.J., S.M. Percival and A.F. Brown. 2002. Nest-site selection by golden
plover: Why do shorebirds avoid nesting on slopes? Journal of Avian Biology 33: 184-190.
Yahner, R.H. and D.P. Scott. 1988. Effects of forest fragmentation on depredation of
artificial nests. Journal of Wildlife Management 2: 158-161.
Beyond Excellence©
81 Governor F.T. San Luis Avenue, Masaya, Bay 4033, Laguna, Philippines
Celfone nos. (063) (049) 0915-360-4660; 0921-374-9752; 0916-526-0164
e-mails: asialifesciences@yahoo.com wsmgruezo@gmail.com
http://journals.uplb.edu.ph/index.php/ALS
©Rushing Water Publishers Ltd., Philippines 2015
Beyond Excellence©
*
Disclaimer: The use of trade names in this publication does not imply
endorsement or criticism of the products named.
Beyond Excellence©
e-mails: asialifesciences@yahoo.com wsmgruezo@gmail.com
http://journals.uplb.edu.ph/index.php/ALS
©Rushing Water Publishers Ltd., Philippines 2015
Beyond Excellence©
CONTENTS
469 A new distribution record of Hoya espaldoniana
Kloppenburg, Siar & Cajano (Section Acanthostemma:
Apocynaceae) A.S. Hadsall, M.A.O. Cajano,
I.A.F. Lambio & M. Alejado
477 Relationship between above- and below-ground
biomass for 18-year-old Abies holophylla under
different stand conditions H.-H. Lee & D.-H. Lee
493 The Philippine genus Stilbotes Stal and a new tribe
of Asopinae (Hemiptera: Pentatomidae) V.P. Gapud
499 Competitive ability of weedy rice against cultivated
rice in the Philippines E.C.Martin & I.R. Tanzo
507 Formulation of an environment and social impact
assessment tool for small scale economic activities in
coastal areas in the Philippines C.A. Cabrido, Jr.
537 Morphological variations of the white goby (Glossogo-
bius giuris Hamilton 1822, Teleostei: Gobiidae) in three
lakes of Southern Luzon, Philippines J.G. Campang &
P.P. Ocampo
Cont. on Next Page
Contents
857 Enhancing learning performance using grouping
optimization based on social relationships and genetic
algorithm C.-Y. Chang, C.-T. Chen, M.-H. Chen,
R.-C. Chen & S.-P. Suen
865 Reviewers -Asia Life Sciences Volume 24, No. 2, 2015
869 Board of Editors -Asia Life Sciences Volume 24, No.2,
2015
Beyond Excellence©
e-mails: asialifesciences@yahoo.com
wsmgruezo@gmail.com
http://journals.uplb.edu.ph/index.php/ALS