Terrestrial BDV Mini Thesis (Fauna)
Terrestrial BDV Mini Thesis (Fauna)
Terrestrial BDV Mini Thesis (Fauna)
JUNE 2023
ABSTRACT
The Philippines holds two-thirds of the world's biodiversity, between 70% and 80% of
all flora and fauna species are found in the country, and it is one of the world's 18
megadiverse countries (Country Profiles, n.d.). Many of the archipelago's islands are thought
to have a very high level of endemism in terms of both land and animal species, with at least
25 genera of plants and 50% of terrestrial fauna present (PhilCHM, n.d.). The Philippines
might actually have a higher biodiversity per unit than other countries (Mona, 2016). A wide
Along with its variety of species, the Philippines is home to 855 globally significant species
of plants, molluscs, elasmobranchs, fishes, amphibians, and reptiles in 228 Key Biodiversity
Areas (KBAs), which are found throughout Southeast Asia (PhilCHM, n.d.).
The Philippine Islands present a remarkable theater for the study of the ecology and
evolution of mammalian diversity. Its islands range in size from less than one hectare to over
100,000 km2, with geological age varying from under 1 million years to over 40 million
years (Heaney et al., 2006). There have been 52,177 identified species found in the
Philippines, at least 50% of which are thought to be endemic (Mona, 2016). The mammals
that have evolved in this diverse archipelago include at least 111 species endemic to the
archipelago out of 172 native terrestrial species; with endemism at 64%, the Philippine fauna
is one of the most distinctive in the world (Mittermeier et al., 1997, 1999; Heaney &
Regalado, 1998).
Undoubtedly, mammals play an important role in ecosystems by providing essential
services such as regulating insect populations, seed dispersal and pollination and act as
indicators of general ecosystem health (Jones & Safi, 2011). As an indicator and umbrella
species of the terrestrial ecosystems, they help to conserve other species and maintain
ecosystem balance (Jorgensen, 2010; Jean-Claude Koffi Bene et al., 2013; Udy et al., 2021).
Particularly, the medium and large-sized mammals are key components of forest and
savannah communities and are therefore considered good indicators of ecosystem health
(Larsen, 2016).
infrastructure, deforestation (Bekker, 2003), tourism practices, hunting, agriculture, and cattle
rearing that affect the demography, population structure, spatial range of individuals and
species, and change in the community structure (Olifiers, 2005). According to the Red List
of Threatened Species (2008), they examined 5, 487 species of mammals, and concluded that
1, 141 are currently on the path toward complete disappearance. The second largest threat to
mammals is hunting for food or medicine. On the positive side, it has been shown that entire
species (such as the African elephant) can recover in areas where hunting has been regulated
and conservation initiatives have been put in place (Faunalytics, 2008). Programs promoting
conservation have been successful in reviving species populations and may help increase the
The fact that the Philippines is being acknowledged as a conservation hotspot, can
mean and give a significant emphasis that the lands that comprise the archipelago have their
own unique level of concern and attention. The Mount Timolan Protected Landscape
(MTPL) is one of the areas of concern in Mindanao that was designated as one of the
protected areas of the Philippines in August 2000. It spans a total area of 2,224.54 hectares
and is located in the border municipalities of Tigbao, Guipos, Lapuyan, and San Miguel in
the province of Zamboanga del Sur (Cudal et al., 2019). Similar to other protected areas in
the country, the MTPL is facing severe threats and has already experienced the loss of
approximately 70% of its natural vegetation. As a result, the MTPL is classified as one of the
Conservation Priority Areas in the Philippines that requires urgent attention and falls into a
high priority category for terrestrial and inland water conservation, according to the
Despite the attention given to the area, previous research conducted in the Mount
Timolan Protected Landscape (MTPL) has primarily focused on a specific group of animals
belonging to the Phylum Chordata, such as birds, freshwater fishes, and amphibians. For
example, Paguntalan et al. (2011) conducted a study in Lake Maragang, the only crater lake
in the MTPL, and documented a total of 93 bird species. Among them, five species were
(IUCN), while 36 species were found to be endemic to the Philippines, and four species were
endemic to Mindanao. Sanguila et al. (2011) also conducted a study in the MTPL and
recorded the presence of vulnerable Ansonia species, specifically the Philippine slender
toads. Cudal et al. (2019) conducted an assessment of the freshwater ecosystem within the
MTPL, with a specific emphasis on the freshwater fish fauna, which revealed the presence of
2,422 individuals representing 12 species from 9 families. However, no studies have been
conducted to evaluate the species composition, richness, and diversity of both flying and
non-flying mammals in the area. Therefore, this study aims to fill this knowledge gap by
providing pioneering data on the species composition, richness, and diversity of volant and
nonvolant mammals within the ecosystem of the Mount Timolan Protected Landscape,
The study aimed to determine the species diversity and distribution of terrestrial
This study provided a list of mammals found in Lake Maragang Rainforest Park,
Tigbao, Zamboanga del Sur. This will also provide information on the anthropogenic
disturbances existing in the area that will be useful for the conservation of these animals.
This study focused on the diversity of terrestrial animals found in Lake Maragang
Rainforest Park, Tigbao, Zamboanga del Sur, and the disturbances affecting the composition
of terrestrial animals, whether anthropogenic or natural disturbances. This is done for 4 nights
and 5 days.
MATERIALS AND METHODS
Sampling Area
The study was conducted in Mount Timolan Protected Landscape, Tibao, Zamboanga
del Sur, Philippines (Fig. 1.). The protected landscape spans 1,994.79 hectares (4,929.2 acres)
and includes a buffer zone of 695.39 hectares (1,718.3 acres). Mt. Timolan is a semi-conical
mountain, rising to 1,177 meters (3,862 ft) above sea level. Specifically, three (3) sites were
established in Lake Maragang Rainforest Park, an area covering 22 hectares in the Protected
Area. It lies within the coordinates 7.7993° N, 123.2653° E, with an elevation of 744 meters
above sea level (Fig.2). The park features a heart-shaped crater lake surrounded by mixed
secondary forests, making it a popular tourist destination. The collection of samples in the
Figure 1. (A) The map of the Philippines and (B) the location of Mt. Timolan Protected
Landscape
Figure 2. Aerial view of Lake Maragang Rainforest Park situated in
Mt. Timolan Protected Landscape.
Study Sites
Bat Sampling
Site 1
The vegetation type in this site is mixed secondary vegetation. Canopy vines,
locally called Balagon and Buyo, were found. Understory plants such as ferns and
carabao grass were also present. The site was dominated by a large fruit-bearing tree
that the locals call “tubog,” which is a ficus tree. Furthermore, the site is at the back
of the camping site, wherein many logs were found for construction materials. Hence,
Site 2
The type of vegetation in this site is a mixed secondary vegetation. Ferns are
also abundant in the site. Grass was not found as understory plants. Ficus trees are
absent, however there were palm trees, malakafe trees, bananas and abaca present.
On-site disturbances such as trails, noise pollution and fallen logs were found in the
site.
Site 3
The site has a vegetation type of mixed secondary vegetation. Buyo and
balagon, which are local canopy vines, are also present. The area has a moderate fruit
tree density consisting of tubog or ficus tree and gmelina, and is approximately 80
meters away from an anthropogenic clearing specifically from the campsite function
Sampling Method
Specifically, a duration of two days was lent for the sampling of bats. The sampling was
conducted at night, in which at exactly five in the afternoon, mist nets were opened in three
(3) selected sites. The nets were then checked every two hours to collect the captured bats. As
for the rodents, a duration of one night was lent for the sampling. Specifically, cage traps
were placed in different three (3) sites to ensure that researchers will be able to apprehend
rodents.
Mist nets
A 12-meter and 100-net night mist nets were placed in an area with large
fruit-bearing trees, like the sacking tree which they locally call “tobog.” The sacking
tree is a species of fig tree, in which fruits, from smaller to larger sizes, are usually
consumed by bats (Kalko et al., 1996). The use of mist nets is a common technique to
capture bats (Ferreira et al., 2021). Specifically, ground mist nets were used in this
Six (6) cage traps were placed in selected areas around the lake, and were
baited with coconut meat and peanut butter. Tree branches near the trapping stations
were marked with a bright-colored ribbon at each site for easy identification. Cage or
live trapping is a common method used in order to capture and monitor small and
non-volant mammals.
Bats
area to reduce additional stress and labeled according to the day and time collected.
The next day, they were brought to the processing area for identification. The
morphological metrics, forearm length (FA), head & body length (BL/HBL), tail
length (TL), and teeth formation were measured using a caliper. Individual age, sex,
and elevation were also noted. The gathered measurements were then used for
taxonomic identification of bat species using Ingle and Heaney's key to the bats of the
Philippine Islands (1992) and a poster checklist. Bats were then fed with sugar
Rodents
Identification was done through visual inspection and morphological analysis on the
specimen inside the trap, and the use of checklist poster of the Mammals of Mindanao
Island and the Non-Flying Mammals of Mindanao Island, Philippines (Heany et al.,
1999) as identification guide. The specimens were released to its habitat after
identification in accordance with the Standard Operating Procedure of Cage Traps for
Attractions, 2023).
Statistical Analysis
In the analysis of mammalian diversity, the species richness, relative abundance, and
species evenness were comprehensively determined and measured using the Paleontological
Statistics software (PAST) (Hammer et al., 2001). The Shannon-Weiner diversity index was
𝑠
𝐻' = − ∑ 𝑝𝑖 𝑙𝑛 𝑝𝑖
𝑖=1
Where H’ is the Shannon-Weiner diversity index and 𝑝𝑖 is the proportion of individuals found
within species.
𝐻'
𝐸 = 𝑙𝑛𝑆
Where E is the diversity evenness, H’ is the Shannon-Weiner diversity index, and S is the
Additionally, Simpson’s dominance index was used to determine how likely two
individuals of the same species were captured at random from an arbitrarily large population
2 𝑛𝑖 2
𝐷 = Σ(𝑝𝑖) = Σ( 𝑁
)
RESULTS AND DISCUSSION
A total of twenty-one (21) individuals from three (3) species of bats were found.
Specifically, there are fourteen (14) individuals of Ptenochirus jagori, five (5) individuals of
Ptenochirus minor and two (2) individuals of Cynopterus bracyotis. All species of bats
belong to the family Pteropodidae. In site 1, nine (9) Pternochirus jagori were found (Table
1). On the other hand, five (5) Ptenochirus minor were captured in site 2 (Table 2). Whilst in
site 3, five (5) Ptenochirus jagori and two (2) Cynopterus brachyotis were found (Table 3).
As for the non-volant small mammals, a total of three (3) rodents were found and identified
to be a Rattus sp., belonging to the family Murinae. Specifically, one (1) Rattus sp. was found
in site 1 (Table 4), zero (0) in site 2 and two (2) in site 3 (Table 5). A graph below shows all
the terrestrial mammals found in Lake Maragang Rainforest Park, Tigabao, Zamboanga del
Figure 1. A graph showing the number of individuals of each terrestrial mammal species found in
Lake Maragang Rainforest Park, Tigabo, Zamboanga del Sur.
Table 1. Bats in Site 1 with notes on their individual age, sex, elevation, forearm length
(FA), head & body length (BL/HBL), and tail length (TL).
Scientific Name Common Elevation Age/Sex FA BL/HBL TL
Name (m) Pregnant (mm) (mm) (mm)
Table 2. Bats in Site 2 with notes on their individual age, sex, elevation, forearm length
(FA), head & body length (BL/HBL), and tail length (TL).
Scientific Name Common Eleva Age/Sex FA BL/HBL TL
Name tion Pregnant (mm) (mm) (mm)
(m)
Table 3. Bats in Site 3 with notes on their individual age, sex, elevation, forearm length
(FA), head & body length (BL/HBL), and tail length (TL).
Scientific Common Elevation Age/Sex FA BL/HBL
Name Name (m) Pregnant (mm) (mm)
Table 1 shows bats captured in site 1. A total of nine bats were captured, belonging to
one species. All individuals were males, with four of them being adults and five being
juveniles. In table 2, five individuals identified to be Ptenochirus minor were captured in site
2, two males and three females. One female was recognized to be pregnant. In table 3, seven
individuals were captured, identified to belong to two species. Five of them were identified as
Ptenochirus jagori, two females and three males, and two of them are Cynopterus brachyotis,
These bats were captured in sites with an elevation of 740 m, with notes on their
Table 4. Rodents in Site 1 with notes on their individual age, sex, elevation, forearm
length (FA), head & body length (BL/HBL), and tail length (TL).
Scientific Common Name Elevation Age/Sex FA BL/HBL TL
Name (m) (mm) (mm) (mm)
Table 5. Rodents in Site 3 with notes on their individual age, sex, elevation, forearm
length (FA), head & body length (BL/HBL), and tail length (TL).
Scientific Common Name Elevation Age/Sex FA BL/HBL TL
Name (m) (mm) (mm) (mm)
The findings presented in Tables 4 and 5 clearly indicate that across all the sites, there
were 3 rodents obtained from site 1 and 3 in an elevation of 740 meters, vouched to be
identified belonging to Rattus sp. All of the rodents were figured to be male, with tail length
ranging from 140-154 mm, with head and body length measurements that varied from 43mm
to 151 mm.
Statistical Analysis
Table 6. Species diversity indices of bats in Lake Maragang Rainforest Park, Tigbao,
Zamboanga del Sur
Site I Site II Site III
Shannon-Weiner 0 0 0.5983
Diversity Index
Evenness 1 1 0.9095
Simpson’s 0 0 0.4082
Diversity Index
Simpson’s 1 1 0.5918
Dominance Index
Bats
It was emphasized that all captured individuals in site 1 belong to P. jagori, and
individuals in site 2 belong to P. minor. While the individuals captured in site 3 comprises
five individuals of P. jagori and 2 individuals of C. brachyotis. In the gathered data of species
evenness (Table 6.), it shows that site 1 and site 2 has a value of 1 which means that the
species found in these sampling sites are evenly distributed compared to site 3 that has a
value of 0.9095. Since, in site 1 it recorded nine individuals of P. jagori and in site 2 it
recorded five individuals of P. minor. However, in site 3, it recorded seven individuals which
belong to two species, the P. jagori and C. brachyotis. Therefore, the species present in site 1
and site 2 are evenly distributed because all the individuals captured are in the same species,
and also were common to the area. This is the opposite case in site 3, which generated 7
individuals, belonging to 2 different species. For the species dominance, site 1 and site 2 has
a value of 1 which means there are no dominant species present in the area compared to site 3
which has a value of 0.5918 wherein two species were recorded in the site, with 1 species
diversity that takes into account both species richness and evenness , site 3 has the highest
diversity as it generated 2 species compared to the other sites that produced individuals
belonging to one species. The Simpson’s diversity index also favors site 3 because it also
takes into account both the number of different species present and their relative abundances.
Thus, site 1 and 2 have evenly distributed species, while site 3 has the highest species
diversity.
With all that was mentioned, it implies that bats have their own habitat preferences
according to the presence of their preferred food. This habitat preference can be observed in
Ptenochirus jagori and Ptenochirus minor were common foragers during fruiting
peaks. They are frugivorous or known to eat primarily on fruits of different plant species
(Bacordo et al., 2019). Specifically, Ptenochirus jagori forage in agricultural areas, tolerate
degraded habitats including urban areas (Mickleburgh et al., 1992), and their population is
thought to be stable (Bacordo et al., 2019). P. jagori is a common Philippine endemic bat
(IUCN, 2020) and can be observed in elevations ranging from 0 to 1, 950 m above sea level
(Heaney et al., 1998). This can explain why most of the bats collected in the area with an
elevation of 740 m above sea level belonged to this species and also dominated sampling
sites 1 and 3. Moreover, there is a connection with these findings to the structure and
vegetation of both sampling sites 1 and 3. As explained in the methodology portion, both
sites have a mixed secondary vegetation. Buyo and balagon, which are local canopy vines,
are also present in both sampling sites. The most important feature of these 2 sampling sites
is that both of the areas have a fruit tree density consisting of tubog or ficus tree and gmelina.
The fruit of this ficus tree is usually relied upon by P. jagori and P. minor (Montefalco &
Nuñeza, 2015 as cited in Del Socorro et al., 2018). It is important to note that this ficus tree is
the dominant tree species in sampling site 1, supporting the results collected that the vouched
samples were all P. jagori. In sampling site 3, despite its similarity to the former site, but the
ficus tree is moderately present in the area, that is why, the samples gathered were not all P.
jagori. However, this ficus tree species, which is tubog, is absent in the second site,
explaining the rationale why the bats individual in the said sampling site did not generate P.
jagori.
Ptenochirus minor or the lesser musky fruit bat does not occur in agricultural or
urban areas and apparently coexists with P. jagori at upper elevations, but it was not observed
in the results (Bacordo et al., 2019). However, some points that were postulated by Bacordo
et al. (2019) were in line with the result in site 2 in which all individuals garnered were
methodology, was observed to have a higher rate of on-site disturbances such as trails, noise
pollution and fallen logs. However, even though destruction of lowland forest habitat leads to
decline, they are still considered to be common and widespread as P. minor can adapt to some
secondary habitats such as the mixed secondary vegetation that characterizes all the sampling
sites, including the second sampling site (Ong et al., 2008). The C. brachyotis occupies a
variety of habitats including primary forest, disturbed forest, mangrove, cultivated areas,
orchards, gardens and urban areas (Zubaid, 1993). This is also proven by the results, and can
be supported by the type of habitat in which this bat species was generated from. The third
sampling site, according to the provided habitat or sampling site description, was
approximately 80 meters away from an anthropogenic clearing specifically from the campsite
variety of habitats including disturbed forest, then the disturbances the sampling site is
receiving minimally affect the distribution of C. brachyotis. Moreover, they were identified
as frugivorous bats, but recognized also to feed on leaves and flower parts of some species of
Rodents
belonging to the Rattus genus, as evidently shown in Table 4 & 5. Since the diversity indices
are commonly applied to communities with multiple species, the obtained samples were
insufficient to undergo computation. However, with the rodents being able to dominate the
area, as it was the only species being vouched for, it can be said that it is not diverse and they
are not also even in terms of distribution. The main reason is that the sampling sites are
relatively disturbed with human activities such as logging which means that they prefer
heavily disturbed forest habitat. To support this result, an article by Loveridge et al. (2016)
stated that black rats have the strongest preference for disturbed habitats associated with
logging. It suggests that disturbed habitats were characterized by a low presence of large
trees, allowing the growth of dense ground and understory vegetation layers. This provides
excellent cover from predators. This postulation was in line with the description of the habitat
in which most of the rodents were collected through live or cage traps. Heavily disturbed
habitats may maximize both predator avoidance and resource availability, making these
habitats desirable for small mammals (Adler & Levins, 1994 & Pardini, 2004). To give a
reason why all the collected rodents belonged to the same species, is because, according to
Shiels et al. (2014), the Rattus sp. are also among the most widespread invasive vertebrates
on islands and continents, and it is nearly ubiquitous on Pacific islands from the equatorial
from three (3) species of bats which are Ptenochirus jagori, Ptenochirus minor, and
Cynopterus brachyotis. These collected bat species belong to the same family Pteropodidae
which are considered as fruit bats. Since the area is surrounded with fig trees which are their
food source, it is the main reason for having many individuals of fruit bat species recorded in
the area. As for the non-volant small mammals, a total of three (3) individuals were found
and identified to be Rattus sp., belonging to the family Murinae. These Rattus sp. were
collected in an area with a lot of shrubs and leaf litters, which are their preferred habitat. In
line with this, we recommend conducting more thorough study to provide standard data to
compute for diversity indices and supporting ecological information. Specifically, the
establishment of sampling sites and in- depth observation of its morphology. To conclude, the
area of Mt. Timolan Protected Landscape has a rich environment that can support these
mammal species.
Mt. Timolan Protected Landscape is a key biodiversity area in the frontier of the
province of Zamboanga del Sur in terms of biodiversity richness and the need to conduct
assessment and monitoring study is vitalin the protection and conservation of the area. The
data gathered presumes that in the future, a frequent and thorough field surveying of the other
sites in the area should also be explored and environmental factors should be quantified.
should be done simultaneously. Monitoring studies are also vital to conduct an inventory on
the fauna species to arrive at a more scientific and robust finding that would be supplemental
for the establishment of the real profile of the fauna population, distribution, and conservation
status of the Mt. Timolan Protected Landscape, Barangay Tigbao, Zamboanga Del Sur,
Philippines.
Collectively, the study was conducted during a limited period wherein no preliminary
survey was done. Therefore, the data acquired on terrestrial mammals is not an efficient
representation of the terrestrial mammalian animals present in the study area since the sites
were chosen randomly. With this, we highly recommend future researchers of Lake Maragang
Rainforest to conduct a preparatory evaluation in the area to establish study sites that would
well-represent the terrestrial mammalian animals to obtain adequate results. Moreover, with
the limited scope of the study, the researchers suggest a wider scope considering that Lake
Maragang Rainforest has a considerable land area. It is to form a more comprehensive and
the identification and processing of the bats and rodents found are based only on their
morphological characteristics. Also, the identification was done in a short duration of time.
Due to these, there were difficulties and skepticism in identifying the species. With this, the
researchers recommend that a longer identification period should be allotted to identify the
level via DNA barcoding to confirm the species. Lastly, the researchers recommend
their acquired data that would guide and help the caretakers of Lake Maragang Rainforest to
Adler, G. H., & Levins, R. (1994). The island syndrome in rodent populations. The Quarterly
Review of Biology, 69(4), 473–490. https://doi.org/10.1086/418744.
Bacordo, C., Marfil, R., & Aries, J. (2019). Fruit bats as natural foragers and potential
pollinators in fruit orchards: a reproductive phenological study. 1(1), 1–9.
Cudal, M. G., Calimbo, L. G. L., Larede, B. G. S., & Locson, J. B. (2019). Freshwater
fish species composition of Mount Timolan Protected Landscape, Zamboanga del
Sur. University of Mindanao International Multidisciplinary Research Journal 4(1):
76-86.
Del Socorro, M. M. L., Enguito, M. R. C., & Mapi-ot, E. F. (2018, August). Species Diversity
of Bats in Clarin River, Misamis Occidental, Philippines. Journal of Multidisciplinary
Studies, 7(1), 209-223. http://dx.doi.org/10.7828/jmds.v7i1.1253
Ferreira, D. F., Jarrett, C., Atagana, P. J., Powell, L. L., & Rebelo, H. (2021). Are bat mist
nets ideal for capturing bats? From ultrathin to bird nets, a field test. Journal of
Mammalogy, 102(6), 1627-1634.
Heaney, L. R., & Regalado, Jr., J. C. (1998). Vanishing Treasures of the Philippine Rain
Forest. The Field Museum, Chicago.
Heaney, L. R., Balete, D. S., Dolar, L. L., & Ong, P. S. (1998b). A Synopsis of the
https://doi.org/10.3158/0015-0754(2006)106[28:SABOTM]2.0.CO;2.
R Pamaong, P. Duya, Alcala, E., Roy, M., Pedregosa, M., Warguez, D., Garcia, H., Lorica, R.,
Ong, P., Ruth Grace Rosell-Ambal, Alviola, P., Ramayla, S., Blas, Apolinario,
Heaney, L., Marie, L., & Carlos, J. (2020, December 15). IUCN Red List of
Name. https://www.iucnredlist.org/species/18653/22071217#geographic-range
Jean-Claude Koffi Bene, E. Anderson Bitty, Kouakou Hilaire Bohoussou, Abedi, M., Gamys,
IN SIME DARBY OIL PALM CONCESSION IN LIBERIA. Glob J Biol Agric Health Sci,
2(3), 93–102.
Jones, K. E., & Safi, K. (2011). Ecology and evolution of mammalian biodiversity.
Philosophical Transactions of the Royal Society B: Biological Sciences, 366(1577),
2451–2461. https://doi.org/10.1098/rstb.2011.0090.
Kalko, E. K., Herre, E. A., & Handley Jr, C. O. (1996). Relation of fig fruit characteristics to
fruit‐eating bats in the New and Old World tropics. Journal of Biogeography,
23(4), 565-576.
Koprowski, J.L. (2005). “The response of tree squirrels to fragmentation: a review and
synthesis,” Animal Conservation, vol. 8, no. 4, pp. 369–376.
Larsen, T. H. (2016). Core standardized methods for Rapid Biological Field Assessment.
Conservation International.
Loveridge, R., Wearn, O. R., Vieira, M., Bernard, H., & Ewers, R. M. (2016). Movement
behavior of native and invasive small mammals shows logging may facilitate invasion
in a tropical rainforest. Biotropica, 48(3), 373–380. https://doi.org/10.1111/btp.12306
Ong, P., Rosell-Ambal, G. & Tabaranza, B., Heaney, L., Pedregosa, M., Warguez, D.,
Ramayla, S., Gomez, R., Gonzalez, J.C. & Pamaong, R. (2008). Ptenochirus minor.
The IUCN Red List of Threatened Species. http://
dx.doi.org/10.2305IUCN.UK.2008.RLTS. T18654A8504183. en.
Mickleburgh, S.P., Hutson, A.M. & Racey, P.A. (1992). Old World fruit bats. An action plan
for their conservation. Gland, Switzerland: IUCN, 263.
Mittermeier, R. A., Gil, P. R., & Mittermeier, Eds., C. G. (1997). Megadiversity: Earth’s
BiologicallyWealthiest Nations. CEMEX, Monterrey, Mexico.
Mittermeier, R. A., Myers, N., Gil, P. R., & Mittermeier, Eds., C. G. (1999). Hotspots,
Earth’s Biologically Richest and Most Endangered Terrestrial Ecosystems.
CEMEX, Mexico City.
Paguntalan, L. M. J., Jakosalem ,P. G., Lagerqvist, M., & Nordin, J. (2011). Bird observations
on the Zamboanga Peninsula, Mindanao, Philippines. FORKTAIL. 27: 15-22.
Olifiers, N., Gentile, R., & Fiszon, J.T. (2005). “Relation between small-mammal species
composition and anthropic variables in the Brazilian Atlantic Forest,” Brazilian
Journal of Biology, vol. 65, no. 3, pp. 495–501.
Sanguila, M. B., Siler, D., Diesmos, A.C., Nuñez, O., & Brown, R.M. (2011).
Phylogeography, geographic structure, genetic variation, and potential species
boundaries in Philippine slender toads. Molecular Phylogenetics and Evolution .
(61): 333–350.
Shiels, A. B., Pitt, W. C., Sugihara, R. T., & Witmer, G. W. (2014). Biology and impacts of
Pacific island invasive species. 11. rattus rattus, the black rat (rodentia: Muridae).
Pacific Science, 68(2), 145–184. https://doi.org/10.2984/68.2.1
Tan, K.H., Zubaid, A. & Kunz, T.H. (1998). Food habits of Cynopterus brachyotis (Muller)
(Chiroptera: Pteropodidae) in Peninsular Malaysia. Journal of Tropical Ecology, 14,
299–307.
Udy, K., Fritsch, M., Meyer, K. M., Grass, I., Hanß, S., Hartig, F. and Wiegand, K. (2021).
Environmental heterogeneity predicts global species richness patterns better than area.
Global Ecology and Biogeography, 30(4), 842–851.
https://doi.org/10.1111/geb.13261.
Zubaid, A. (1993). A comparison of the bat fauna between a primary and fragmented secondary forest
in Peninsular Malaysia. Mammalia, 57(2), 201–206.