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CHAPTER I
Introduction
The complexity of tropical mountain ecosystems has long provided haven for various
Philippine wildlife species. The elevational gradients provide various forest types while vertical
stratification of trees offer habitat to species of different niches. It is no wonder then that forest
destruction has been identified as the primary threat to Philippine wildlife (Rickart et al. 2007).
This has also been the leading threat listed for many Philippine wildlife species.
However, one of the most overlooked threats is the negative ecological impacts of introduced
small non-volant mammals on native and endemic wildlife species. A mammal is a vertebrate
animal of the class Mammalia. Mammals are characterized by the presence of milk-producing
mammary glands for feeding their young, a neocortex region of the brain, fur or hair, and three
middle ear bones. These characteristics distinguish them from reptiles and birds, which they
diverged from in the Carboniferous Period over 300 million years ago. Around 6,4000 extant
species of mammals have been described and divided into 29 orders. Nonnative rats have been
reported to cause extinctions on islands and cause severe biodiversity loss (Amori and Clout
2003; Howard et al. 2007; Jones et al. 2008; Ruffno et al. 2009).
The terrestrial mammalian fauna of the Philippines has traditionally been divided into
four major regions, based on richness, composition and degree of endemism (Steere, 1890;
Heaney & Rabor, 1982): the Palawan, Mindanao, Luzon and Negros regions. Additionally,
several large oceanic islands (Mindoro) often are mentioned as distinct. These parallel the faunal
regions exhibited by birds (Dickerson, 1928), and reptiles and amphibians (Brown & Alcala,
1970), and correspond to the limits of late Pleistocene islands (Heaney, 1985b). The following
brief descriptions of the faunal regions are intended to provide a general perspective. It should be
noted that thorough faunal surveys and reports for all of the regions are badly needed, especially
The mammalian fauna of the region is also remarkably diverse. The Philippine islands
support at least 17 endemic genera of rodents, two of insectivores and four of bats, as well as
many endemic species of more widespread genera. Many of these endemics are restricted to one
or a few islands and short distances separate faunas that are quite distinct (Heaney, 1985b). This
is unlike the pattern of the mammalian fauna on the islands of the adjacent Sunda Shelf. On this
vast continental shelf, the proportion of endemics is much lower, and widely separated islands
The largest order of mammals, by number of species, are the rodents, bats, and
Eulipotyphla (including hedgehogs, moles and shrews). The next three are the Primates
(including humans, monkeys and lemurs), the even-toed ungulates (including pigs, camels, and
whales), and the Carnivora (including cats, dogs, and seals). Lewis, Charlton t.; Short, Charles
(1879).
various ecosystem services that are crucial for human well-being ranging from maintaining
biodiversity and their habitats from pollination, seed dispersal, insect-pest control and ecosystem
engineering (Lacher et al., 2019). Despite the crucial role of mammals in ecosystem,
approximately 25% of all mammals are threatened with extinction and the major threats to their
survival are habitat loss and degradation, and biological resource extraction (Schipper et al.,
2008; Ceballos et al., 2020). Many species of mammals, went extinct in the last century and
The insufficient studies on mammals in the area may have led to the poor understanding
and underestimation of the diversity of this group of fauna. Similarly, few studies have
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quantitatively explored how species assemblage of mammals varied with habitat types as well
Therefore, this mammalian fauna survey/study will be conducted to generate the needed
information on available species found in the area, describe their types of diet, appearances and
habitat, conservation status and activation. The locale of the study will be conducted in Barangay
Nabalawag, Municipality of Barira, in the province of Maguindanao del Norte. Its population as
determined by the 2020 Census was 3,252 (PSA Website). This represented 9.00% of the total
of Mindanao. Elevation at these coordinates is estimated at 545.6 meters or 1,790.0 feet above
most endangered groups. Their value seems still to be underestimated by society and is based on
many misconceptions and a simple lack of knowledge, which in turn might influence society’s
willingness to protect these animals. The researchers investigated about mammals, then designed
a teaching sequence in order to trace some possible conceptual changes and to shape pro-
Moreover, finding solutions to counter mammals declines and extinctions is one of the
greatest conservation challenges, which comes with alarming and serious implications for the
The general objective of the study is to determine which species of Mammalia are
presents in the forest areas of Barangay Nabalawag, Barira, Maguindanao Del Norte.
1. Identify the local name, common name, scientific name, and family name of the mammals
2. Determine the description (Diet, Physical Appearance and Habitat) of the mammals found in
3. Determine the conservation status (Critical Endangered, Threatened, Vulnerable and Least
Concern) of each mammal found in Barangay Nabalawag, Barira, Maguindanao Del Norte.
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- Local Name
Identification
- Common Name
- Scientific Name
- Family Name
- Diet
*Carnivore
Description *Herbivore
M *Omnivore
- Physical Appearance
A
- Habitat
M
M -Critical Endangered
A -Threatened
IUCN Conservation
-Vulnerable and
L Status
-Least Concern
SG
-Nocturnal
The result of this study will become as baseline data and information on the mammalian
fauna in the municipality of Barira. It will also serve as a guide and reference for the future
researchers, academe, DENR, and LGU. It will also enlighten the policy maker to formulate
resolutions and policies for the preservation, conservation and protection of the mammals toward
sustainable ecosystem.
(IUCN) conservation status and activation status of each species of mammal in Barangay
Mammalia, it is characterized by the presence of milk producing mammary glands for feeding
their young, a neocortex region of the brain, fur or hair, and three middle ear bones.
Identification. The process of identifying the mammals by its local name, official
Terminologies
Classification. Refers to the categorization, the process in which ideas and object are
Least Concern. A taxon is when it has been evaluated against the Red List criteria and
Norte.
Transect Walk. An exercise that entails walking between two points to intentionally
cross or transect a community, explores environmental and social resources, conditions and
habitat.
Vulnerable. When the best available evidence indicates that it meets any of the criteria A to
E for Vulnerable, and it is therefore considered to be facing a high risk of extinction in the wild.
CHAPTER II
Invasive species play a key role in the decline of native species (e.g., Miller et al. 1989;
Atkinson 1996), the disruption of ecological communities (e.g., Sanders et al. 2003), and the
concern (Usher et al. 1986; Wilcove et al. 1998; Harris and Yalden 2004). Early detection of
effort, for example, in control of numbers or eradication (Myers et al. 2000; Mehta et al. 2007).
Indeed, if an invader becomes established and expands its range rapidly, eradication becomes
increasingly more impractical and economically challenging. Thus, immediate action is often the
only opportunity for cost-effective eradication (Stokes et al. 2006). Population conservation and
management are dependent upon knowledge of the target species distribution and abundance
hares and jackrabbits) conventionally uses direct observation such as line-transect surveys
(e.g., Smith and Nudegger 1985) and Distance Sampling (e.g., Reid et al. 2007), or indirect
methods such as faecal sampling (e.g., Forys and Humphrey 1997). Distance Sampling
population densities in a wide variety of taxa, e.g., the red fox Vulpes vulpes (Ruette
(Norvell et al. 2003).
Distance Sampling relies on four assumptions: (1) all targets are detected with certainty
at zero distance from transects; (2) targets are detected at their initial location; (3) distance
measurements are exact (or at least not consistently biased); (4) transects are positioned
randomly with respect to animal density; and (5) the area surveyed is representative of the entire
area (Buckland et al. 1993). The estimation of densities and abundances rely on detection
functions which model the probability of detection, given the distance of targets from transects.
By fitting detection functions to the recorded distance of targets from transects, researchers are
able to estimate the number of targets which were not detected during the survey.
as a minimum of 60–80 detections are required to obtain a smooth detection function (Buckland
et al. 1993), thereby limiting its site-specific application for species that are detected
infrequently, such as those that are cryptic, rare or occur at low-density (including recently
introduced invaders). In contrast, remote sensing using modern camera traps provides a reliable
means of detecting the presence of elusive, rare, cryptic, and nocturnal species with minimal
disturbance (Cutler and Swann 1999; Silveira et al. 2003) as they can be left recording
continuously in situ. Estimating density and abundance from camera trap data was restricted
However, species which do not exhibit individual markings often account for a large
proportion of a recorded assemblage (Carbone et al. 2001). Several species which lack unique
markings have been subject to capture-recapture population estimation (e.g., Trolle et al. 2006;
Kelly et al. 2008), but these studies fail to account for identification error (Oliveira-Santos
et al. 2010). Thus, this approach is unsuitable for species without unique markings (for e.g.,
estimating population densities for unmarked populations from a variety of survey data
(Chandler and Royle 2013). However, this method lacks precision at smaller sample sizes.
The random encounter model (REM) provides a means of estimating population densities
for species where individuals cannot be recognized reliably, by modeling animal movement
processes and contact with cameras (Rowcliffe et al. 2008). The REM relies on three
assumptions: (1) the movement of the targets is random; (2) detections represent independent
contacts between cameras and animals; and, (3) the population is closed. Studies utilizing the
REM will inherently violate one or more of these assumptions (e.g., the movement of animals in
the landscape is never truly random). However, the model is considered to reasonably robust
against certain violations of the assumptions (e.g., nonrandom movement due to interactions with
et al., 2012). The method does of course have inherent constraints, the most significant being
estimations of group size and speed of movement, which may differ within species depending on
habitat or prevailing environmental conditions. Furthermore, due to the requirement for random
camera placement, rare species may be detected too infrequently for density estimates to be
calculated (Rowcliffe et al. 2008). The REM has been used for a variety of medium-small
harveyi (Rovero and Marshall 2009). Where cross-validation has been attempted, the REM
using both camera trap capture-recapture and line transect Distance Sampling models (Zero
et al. 2013).
Used of remote-sensing camera trap REMs to estimate the density of two sympatric
leporid species (one native, of conservation concern, and one invasive nonnative), and describe
the invasive-native species replacement process. We discuss the spatial dynamics of replacement
between native allopathy and shallow or deep sympatry (i.e., the outer 100%, or inner 50%,
minimum convex polygons representing the range of the invasive species) in the invader's
peripheral and core ranges. We used conventional line transect Distance Sampling to corroborate
the spatial pattern of invasive-native replacement. We also describe a means by which future
surveys could minimize survey effort in terms of the numbers of cameras used per unit area and
the number of days during which they are deployed. Consequently, we provide explicit
guidelines for the future monitoring of this particular species replacement process. Such data will
provide a greater understanding of the invasive-native species dynamic and inform population
management measures.
The mammalian fauna of the SE Asian islands has been affected in complex ways by the
size, isolation and geographical history of the islands. The Philippine islands (excluding
Palawan) are the most isolated of the islands considered here, having arisen de nouo from the sea
13
floor. The Palawan chain has been less isolated, having been joined to Borneo by a broad land
bridge during the mid-Pleistocene. Non-volant mammals have entered the archipelago
predominantly from Borneo, which is the nearest continental shelf land mass, by dispersal over
These barriers continue to be the major factors defining the distributions of species.
Extinction on the Palawan chain was probably very high following its initial isolation from
Borneo, but after about 160 000 years it retains a large and diverse fauna in which extinction is
low and speciation does occur. Speciation elsewhere in the region has contributed substantially
to the total faunal richness, with 55-70% of the fauna of Luzon having arisen in such a manner.
The results of this study indicate that the rate of colonization by non-volant mammals across
landbridges is typically quite high. On the Sunda Shelf islands, levels of endemism are low and
most endemics are limited to montane vegetation; nearly all lowland species are widespread. In
the Philippines, small islands that were part of the late Pleistocene Island of Greater Mindanao
share the same species and populations of some species (e.g. pygmy squirrels; Heaney, 1985)
On the other hand, narrow sea-water channels between islands have served as major,
nearly insurmountable barriers to many non-volant mammals. Large but geologically young
islands separated from rich faunal sources by 5-20 km of sea water have extremely depauperate
faunas. For a large island such as Negros, with about five indigenous species, a rough estimate of
one colonization event per 250000 years is likely to be a maximum rate. Data from Mindoro and
Camiguin support this estimate. Because the fossil record from the Philippines is very poor it is
not possible to measure directly the rate of extinction. However, a comparison of two sets of
The Palawan chain was isolated from Borneo about 160000 years ago, whereas islands on
the central Sunda Shelf were isolated only about 10000 years ago. The fauna of the Palawan
chain is about 50°j0 smaller than the faunas on comparably sized islands that are on the shallow
portion of the shelf, so that an estimate of 1-2% extinction/l0000 years is indicated. Given the
low colonization rate and non-trivial extinction rate, how is it that an isolated island such as
Luzon has any non-volant mammals at all? The data cited above clearly demonstrate that
speciation is the crucial variable. At least 55% of the non-volant mammals on Luzon have
resulted from speciation within the archipelago, and an estimate of 70% may be more accurate.
evolution (Carlquist, 1974; Patton, 1984), but it is rarely directly included in studies that utilize
the equilibrium model (but see MacArthur & Wilson, 1967: 173). We need more phylogenetic
analyses to allow measurement of indigenous speciation rates in order to determine the effects of
body size, trophic level and other variables on speciation rate. Data in this paper lead me to
predict that speciation rate will be related to colonization rate in a complex fashion, with
speciation rate initially increasing as colonization rate increases to some low level (providing the
raw material for speciation), and decreasing thereafter as colonization rate increases. I know of
no data that could be used to test this prediction, but its testing is fundamental to development of
the triradiate equilibrium model discussed earlier. Trends in endemism related to age, isolation
and area of islands have been discussed here, but sample size was small and only rudimentary
statistical analysis was attempted. A correlation between area and percentage endemism has been
noted among birds (see MacArthur & Wilson, 1967: 174; Case & Cody, 1983: 334) but not
previously noted among mammals. A quantitative analysis of a larger data set is needed. Finally,
I must add an explicit plea for research of the most fundamental sort. All of these studies are
15
predicated on the availability of accurate taxonomic data, and yet the distributions and systematic
relationships of many, if not most, insular mammals are poorly known, especially in the tropics.
data.
Modern conservation biology has two fundamental goals: (1) preservation of natural
communities that are representative of the biotic regions of the world; and (2) prevention of
extinction of species. Several conclusions drawn in this paper have direct implications for the
conservation of non-volant mammals in SE Asia. First, each area that is defined by historical
events (e.g. Pleistocene islands) is likely to support endemic species. Even small islands often
endemism. Secondly, within a given biotic region (such as those defined by Pleistocene islands)
most species of mammals will occur on the largest islands. Reserves might profitably be located
on these high-diversity islands. Thirdly, extinction is area dependent; thus, large parks will
support more species than small parks (the SLOSS debate; see Newmark, 1986).
extinction, and they may often require special protection and management efforts. Fourthly, most
extinction in reserve areas will probably take place within several hundred years after isolation of
the reserve from other suitable habitat. Given the evidence presented here for high colonization
rates across suitable habitats and very low colonization rates across hostile habitats, the
colonization and speciation by non-volant mammals usually occur on a time-scale that prevents
CHAPTER III
RESEARCH METHODOLOGY
This chapter presents the location of the study, research design, research instruments,
sampling procedure, data gathering procedure and data analysis of the study.
Del Norte which lies in the coordinate of latitude 7° 28' 40" north and longitude 124° 18' 01"
east. It has a total land area of 5843.3594 hectares with 3,917.2 hectares of forestland.
17
Figure1. The location of the study and reference Map of Philippines, Map of Mindanao, Map of
Research Design
The research design that will be used in the study is descriptive survey which includes
identification, description, provision of the IUCN conservation status and activation status of
Sampling Procedure
The sampling procedure that will be used in the study will be by establishing transect walk
observation to the purposive strategic sampling area within Barangay Nabalawag, Barira,
Maguindanao Del Norte. And every walk will be recorded via GPS tracking app.
The researchers will use instrument such as: camera for taking photographs in every
The data gathered will be identify by its family name, scientific name, common name,
local name. To describe characteristic such as diet, physical appearance and habitat. To
determine IUCN conservation status critical endangered, threatened, vulnerable, least concern
and to determine the activation status nocturnal, diurnal, crepuscular of mammal found in
Data Analysis
All data gathered will be analyzed using descriptive statistic. The data will be ranked
tabulated according to its Identification, Description, Conservation Status and Activation Status
and number of individuals seen during observation.
19
CITED LITERATURE
Bachman, S. B., Lewis, S. D. & Schweller, W. J., 1983. Evolution of a forearc basin, Luzon
Barbehenn, K., Sumangil, J. P. & Libay, J. L., 1973. Rodents of the Philippine croplands.
Bartlett, A. S. & Barghoorn, E. S., 1973. Phytogeographic history of the isthmus of Panama
during
the past 12000 years (a history of vegetation, climate, and sea-level change) In A.
Amsterdam: Elsevier.
Bloom, A. L., 1983. Sea level and coastal morphology of the United States through the Late
Minnesota Press.
American Naturalist, BROWN, J. H., 1978. The theory of insular biogeography and the
Brown, W. C. & Alcala, A. C., 1970. The zoogeography of the herpetofauna of the
20
Philippine Islands, a CARLQUIST, S., 1974. Island Biology. New York: Columbia
University Press.
Case, T. J. & Cody, M. L., 1983. Island Biogeograpb in the Sea of Cortk Berkeley: University
Darlington, P. J., 1957. <oogeograpb: the Geographical Distribution of Animals. New York: J.
Wiley.
Extinctions:
Dickerson, R. E., 1928. Distribution of life in the Philippines. Monographs ofthe Bureau of
Science, Manila, 2:
D. E. Hayes (Ed.), The Tectonic and Geological Evolution of Southeast Asian Seas and Islands.
Everett, A. H., 1889. Remarks on the zoo-geographical relationships of the island of Palawan
and some adjacent islands. Proceedings of the <oological Society of London, 1889: 220-
228.
Fox, R. B. & Peralta, J. T,, 1974. Preliminary report on the paleolithic archeology of the
Cagayan
21
Valley, Philippines, and the Calawanian industry. Proceedings of the First Regional
Museum.
Gascoyne, M., Benjamin, G. J. & Schwartz, H. P., 1979. Sea-level lowering during the Illinoi
annlaciation: evidence from a Bahama ‘‘blue hole”. Science. 205: 806-808.105: 467-
the California Academy of Sciences, 38: 105- 130. Press. of Maine. Biological Journal of
the Linnean Sociely, 28: 37-64. 191-246. Chicago: University of Chicago Press.
Gilbert, F. S., 1980. The equilibrium theory of island biogeography: fact or fiction? Journal of
Biogeography, 7: 209-235.
Groves, C. P., 1969. Systematics of the anoa (Mammalia, Joytapa). Beaufoortia, 17: 1-12.
GROVES, C. P., 1981. Ancestors for the pigs: taxonomy and phylogeny of the genus Sus.
Groves, C. P., 1983. Pigs east of Wallace’s Line. Journal de la Societe des Oceanistes, 39: 105-
19.
Groves, C. P., 1984. Mammal faunas and the paleogeography of the Indo-Australian region.
Courier
22
Groves, C. P., 1985. Plio-Pleistocene mammals in island Southeast Asia. Modern Quaternary
Studies in
Grubb, P. & Groves, C. P., 1983. Notes on the taxonomy of the deer (Mammalia, Cervidae) of
the
Hamilton, W., 1979. Tectonics of the Indonesian region. Geological Survg Professional Papers,
1078: 1-345.
Hanski, I., 1986. Population dynamirs of shrews on small islands accord with the equilibrium
model.