Present distribution, population status, and conservation of
Western Hoolock Gibbons Hoolock hoolock
(Primates: Hylobatidae) in Namdapha National Park, India
AwadheshKumar 1, P.P. Mary 2 & Pushkal Bagchie 2
1 Lecturer, 2 Department
of Forestry, Northeastern Regional Institute of Science & Technology
(NERIST), Deemed University, Nirjuli, Itanagar, Arunachal Pradesh 791109, India
Email: 1 reshi123in@yahoo.co.in , tpileatus@gmail.com
Date
of publication 26 April 2009
ISSN
0974-7907 (online) | 0974-7893 (print)
Editor: Mewa Singh
Manuscript
details:
Ms
# o1955
Received
29 February 2008
Final
revised received 09 September 2008
Finally
accepted 11 November 2008
Citation: Kumar, A., P.P.
Mary & P. Bagchie (2009). Present distribution,
population status, and conservation of Western HoolockGibbons Hoolock hoolock(Primates: Hylobatidae) in NamdaphaNational Park, India. Journal of Threatened Taxa1(4): 203-210.
Copyright: © Awadhesh Kumar, P.P. Mary & Pushkal Bagchie 2009. Creative Commons Attribution 3.0 Unported License. JoTT allows
unrestricted use of this article in any medium for non-profit purposes,
reproduction and distribution by providing adequate credit to the authors and
the source of publication.
Author
Details: Dr. Awadhesh Kumar is an animal
behavioral ecologist and wildlife conservationist. He has obtained his Masters
degree in Forestry, Wildlife & Environmental Science from G. G. University,Bilaspur, and completed his doctorate degree from
North-Eastern Hill University Shillong in Zoology
(Wildlife Behavioural Ecology). He joined as faculty of Department of
Forestry at NERIST in June 2006 and is engaged in teaching wildlife ecology,
management, and conservation to undergraduate and post-graduate students of
forestry.
Dr. (Mrs.) P. P. Mary is an animal biologist. She completed her doctorate from the Centre
of Advanced Study in Marine Biology, AnnamalaiUniversity (Tamil Nadu). She joined as faculty of Forestry at NERIST in
February 1986 and is engaged in teaching wildlife resources utilization and
conservation to undergraduate and post-graduate students of forestry.
Mr. Pushkal Bagchie is a student of B.Sc. Forestry and has completed
his graduate degree from NERIST in Forestry and is presently pursuing a post
graduate degree in forestry from ICFRI, Dehra Dun.
Author
contributions: Pushkal Bagchie collected the data in the field
on population status of Hoolock Gibbon in Namadapha. Awadhesh Kumarand P.P. Mary assisted in the
analysis and compilation of field data, and in writing of manuscript.
Acknowledgement:We would like to thank Mr. M.K. Palit,
Deputy Conservator of Forest (Wildlife), Department of Forests, Govt. of Arunachal Pradesh for providing us with the
permission to carry out this work in NamdaphaNational Park. We also thank the Field Director, NamdaphaNP and Dr. Chandiramani, Research Officer and his
field staff for the necessary logistic and manpower support for the successful
completion of the work. We offer our sincere thanks to the Director, NERIST and
Dr. P. Rethy, Head, Department of Forestry for
providing the necessary facilities and help during the study. We are particularly grateful to Mr. C. Loma,
Deputy Chief Wildlife Warden for providing photographs and information on
gibbon, Mr. Tai Dora for his physical help during field work, Dr.Dibyendu Adhikari and Dr. Atiqur Rahman, for sharing much
of their vital information regarding NamdaphaNational Park. We
finally thank all the reviewers for critically evaluating, editing and giving
constructive suggestions for improving the standard of the manuscript and Mr.Raju Barthakur, Lecturer in
English, Department of Humanities and Social Sciences, NERIST for
Linguistic suggestions and editing.
Abstract: A survey on the present distribution,
population status and conservation of Western HoolockGibbon (Hoolock hoolock)
was conducted from September 2006 to April 2007 in NamdaphaNational Park, Arunachal Pradesh, northeasternIndia. The data were recorded from 12
localities in the Park: Gibbon land, Baghnallah, Deban, 15th Mile, 16th Mile, Hawaghar,
19th Mile, Haldibari, Hornbill camp, Baranallah, Firmbase camp, and Embyong. A total of 50 individuals in 20 groups were
recorded during the census by using direct and indirect methods. Out of 20 groups, nine groups were observed
through direct visual observation. The
remaining 11 groups were estimated by using indirect observation methods such
as songs, calls, and branch shaking. The
composition of the population was 19 adult males (38%), 19 adult females (38%),
and 12 immatures (24%). The group size was estimated as 2.5 individuals
per group. Anthropogenic disturbances
observed in the gibbon habitat were habitat loss, hunting and poaching, canopy
gaps, livelihood issues for local people, and
livestock grazing.
Keywords:Canopy gaps, conservation, distribution, HoolockGibbon, Namdapha National Park, population status.
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Introduction
India
has 32 taxa of primates in the wild (Molur et al. 2003). Of these, the Western Hoolock Gibbon Hoolock hoolock and
Eastern Hoolock Gibbon Hoolock leuconedys are two species of lesser apes found
in India (Das et al. 2006). The Hoolock Gibbon was formerly associated with genera Hylobates (Prouty et al. 1983a, 1983b) and Bunopithecus(Brandon-Jones et al. 2004; Groves 2005). Today it is classified in the genus Hoolock(Mootnick & Groves 2005) with two species:
Western Hoolock Gibbon Hoolock hoolock from northeastern India south of the
Brahmaputra River (Mukherjee 1982; Alfred & Sati
1986; Choudhury 1987), Bangladesh (Anderson 1878; Siddiqi 1986; Das et al. 2003a) and western Myanmar (Tickell 1864), and Eastern HoolockGibbon H. leuconedys from LohitDistrict of Arunachal Pradesh, India (Das et al. 2006), Myanmar and China
(Groves 1971; Anderson 1978; Lan 1994). The Debang-Bramhaputrariver system in the west (Tilson 1979) and Chindwin
in the east act as physical barriers for the distribution of species (Parsons
1941; Groves 1967, 1972; Choudhury 1987). In India and Bangladesh, the Hoolock range is strongly associated with the
occurrence of contiguous canopy, broad-leaved, tropical wet evergreen and
semi-evergreen forests.
The
population of H. hoolock in the wild has
declined by more than 90% over the past three decades due to numerous anthropogenic threats
(Walker et al. 2007). The debilitating
threats include habitat destruction and fragmentation as a result of
agricultural expansion, shifting cultivation, establishment of tea gardens,
coffee estates, logging, developmental projects, and hunting and poaching for
food, traditional medicine, body parts, pet collection, and illegal trade (Choudhury 1990, 1991, 1996a; Mukherjeeet al. 1992; Srivastava 1999; Ahmed 2001; Malone et
al. 2002; Solanki & Chutia2004; Das et al. 2006; Walker et al. 2007). These threats occur in Arunachal Pradesh as
well as in other areas of its distribution (Srivastavaet al. 2001a, 2001b) and may have a direct impact on the population growth and
distribution pattern of Hoolock hoolock due to its dependency on forest canopy for
habitat, its being frugivorous, a brachiatorand its territorial behaviors. Owing to
its being frugivorous, the species plays a vital role
as a seed disperser and pollinator (Howe 1986; Terborgh1990) in lowland tropical rain forest ecosystems. Because of the evidence of widespread and
rapid population decline, H. hoolock is listed
by the IUCN Red List of Threatened Species as Endangered (Brockelmanet al. 2008). In Bangladesh it is categorised as Critically Endangered, while in India it is Endangered as per the IUCN Regional Red List (Molur et al. 2003). In India the species is listed in Schedule I of the Indian Wildlife
(Protection) Act 1972, and also in Appendix I of CITES. Against such a backdrop
and the importance of the species for conserving the forest ecosystem, we
realized that there still are various gaps with respect to the conservation of H.hoolock in Arunachal Pradesh. These gaps in our
knowledge require immediate attention to save this species from its current
threat status and were the impetus of this study.
Most
of the studies on the Western Hoolock Gibbon’s
population and distribution status have been conducted in northeastern India
including Assam (Choudhury 1990; 1996a, 1996b, 2000,
2001; Das et al. 2003a, 2003b, 2004, 2005, 2006a, 2006b), Meghalaya (Tilson 1979; Alfred & Sati 1986, 1990; Chaudhury 1998, 2006; Gupta & Sharma 2005a), Mizoram (Misra et al, 1994; Gupta & Sharma 2005b; Chaudhury 2006), Tripura (Das et al. 2005; Gupta & Dasgupta 2005), Nagaland (McCann 1933; Chaudhury2006) and Manipur (Chaudhury 2006). A few studies were conducted between 1988 and
2003, and these were concerned only with general distribution patterns (Mukherjee et al. 1988, 1991-92; Borang& Thapliyal 1993; Singh 2001; Chaudhury2003). The sole exception is Chetry et al. (2003) who
conducted a quantitative study on the population status of gibbons in Namdapha National Park (NNP), Arunachal Pradesh. Gibbon habitat has been severely affected by
anthropogenic causes during the intervening period and no quantitative
distribution and population status has been conducted. Therefore, in this article we present
quantitative information on the present distribution, population status, and
conservation of H. hoolock in NNP and compare
our results with those of previous studies.
Materials and Methods
Study Area:
Namdapha National Park
(27023’30’’-27039’40’’N & 96015’2’’-96058’33’’E) is located in the
easternmost part of Arunachal Pradesh in ChanglangDistrict. It has an area of 1985km² with
a core area of 1808km². The park is
bordered on the north by the Kamlang Wildlife
Sanctuary and to the west by the Noa-dihingRiver. To the south and southeast lie
high mountain ranges and the international border with Myanmar. It is contiguous with reserve forests and
sanctuaries to the south and west, which act as buffer zones. Due to altitudinal variation (200-4571m), the
climatic conditions are heterogeneous across the park. The temperature varies from 350C to 00C at lower altitudes and ranges to below freezing at
higher elevations. The annual precipitation ranges from a minimum of 1400mm to
a maximum of 2500mm, 75% of which falls between April and October. Relative humidity remains high except during
the winter months, and annually it varies from a minimum of 47% to a maximum of
93%.
There
are three major forest types -- tropical, temperate and alpine forest (Champion
& Seth 1968) in NNP. The highly
diverse flora of NNP includes 73 species of lichens, 59 species of Hepaticae (Bryophytes), 112 species of Pteridophytes,
five species of gymnosperms, and 870 species of angiosperms (Hajra 1996). A total
of 200 plant species belonging to 73 families was recorded by Nath et al. (2005) in three stands of NNP. The predominant vegetation at lower
elevations is the tropical wet evergreen forest dominated by Dipterocarpus macrocarpus,Shorea assamica, Mesua ferrea, Altingia excelsa, Elaecocarpus aristantus, and Terminalia myriocarpa and reaching a height of 50m.
Faunal
diversity is also high in Namdapha. Ninety-six species of mammals, 233 species of
birds, 76 species of fish and 25 species of amphibians have been reported here
(Ghosh 1987). Besides these, invertebrates included 188 species of beetles, 102
butterflies, 35 moths, 24 Hemiptera, and 115 Mantodea (Ghosh 1987). Similar to other protected areas in the
region, NNP has 27 villages, made up of 1420 households and a tribal population
of 9618 people, in and around the park (Arunachalamet al. 2004). The Chakma(3951 individuals), a Tibeto-Burman tribe, dominate the local population
followed by Nepali, Lisu, Lama, and Mishmi (Table 1).
Methods
The
present distribution and population status of H. hoolockwas carried out at 12 specific localities in NNP from September 2006 to May
2007 based on information gathered from the literature, forest department, and
local inhabitants. The population was
estimated by a modified line transect method (Burnham et al. 1980; NRC 1981)
and direct count method in different forest types. The line transects were laid in a stratified
random manner to cover all selected areas in the park. Three observers walked slowly covering a
distance of between 10 and 15 km per day between 0600hr and 1730hr or until
sunset. While sighting the presence of
gibbon by direct or indirect methods, such as calls, branch shaking, and sounds
associated with locomotion and feeding, observers recorded the exact count of
each group size, composition, and sex in addition to vegetation type and
evidence of anthropogenic disturbances in its habitat. Age and sex compositions of H. hoolock were classified into two major age categories,
adult and immature; these were further subdivided into four subcategories,
adult, sub-adult, juvenile and infant, based on morphological differences as
described by Gupta et al. (2005).
Results
Population
distribution
The
population survey was mostly concentrated in the buffer zone areas of NNP
except for a few areas of the core zone. The core zone of the park is completely inaccessible due to dense
vegetation and hilly terrain. Nine
populations of H. hoolock were found
throughout the entire tropical evergreen forest of NNP and three populations
were recorded from sub-tropical moist-deciduous and bamboo thick forest. They occur in all the different tree
associations and were observed at altitudes from 150 to 800m. The majority of the groups were sighted at an
elevation of 500m. They were found to be
sympatric with the Capped Langur (Trachypithecus pileatus).
Ninety-five
km of transects were laid and surveyed for the presence of H. hoolock in 12 different localities of NNP (Table
2). In these 12 localities we recorded a
total of 20 groups. Eleven groups (55%) were recorded by indirect
observations, with nine groups (45%) observed directly. The majority of the NNP gibbon
population (17 groups) was recorded in tropical evergreen forest. Of the 20 groups, 12 groups (60%) were
recorded from four localities namely Gibbon land, Hawaghar,
Hornbill camp, and Firmbase camp.
Group
composition and size
A
total of 50 individuals were recorded in the 20 groups during population
estimation. The group size and
composition of the population surveyed in different localities are presented in
Table 2. The smallest group contained a
single sub-adult solitary male. Of the
50 individuals, 19 (38%) were adults males, 19 (38%) were adults females, 2
(4%) were sub-adults, 2 (4%) were juveniles, and 8 (16%) were infants (Fig.
1). The sub-adults, juveniles, and
infants formed the immature class comprising 24% of the total population. The average group size was estimated to be at
2.5 individuals, ranging from 1 to 4 individuals. The estimated adult sex ratio
was 1:1.
Temporal
sighting period of Hoolock Gibbon in Namdapha National Park
Gibbon
sightings at NNP were recorded from 0600hr until the end of sunset. The highest number of
groups (30%) were sighted just after sunrise between 0600hr and 0700hr
followed by the second highest number of groups (20%) between 0700hr and 0800hr
(Fig. 2). No gibbon sightings were
recorded between 1000hr and 1400hr.
Anthropogenic
disturbance and conservation:
Table
3 expresses the presence of anthropogenic pressure on NNP. While evidence of hunting and poaching was
recorded in all 12 surveyed areas, timber logging and agricultural activities
were absent from the surveyed areas. Hunting, illegal fishing, and trapping of wild fauna like Tiger, Barking
Deer, Leaf Deer, Sambar, bear, wild cat, and a
variety of birds by local inhabitants, particularly the Lisu,Chakma and Mishmi tribes
for bushmeat and their body parts, was a very common
phenomenon. Livestock grazing and human
settlement were recorded only in the Deban area and
in the periphery of the park. Collection
of non-timber forest produce (fuelwood, medicinal
plants, wild vegetable and housing materials) and tourism pressure were
recorded in the Gibbon Land, Baghnallah, Deban, Fifteenth Mile, Hawaghar, Haldibari, and Hornbill camp sites. All of these areas are located inside the
buffer zone of NNP.
Discussion
Hoolock hoolock survive primarily in tropical evergreen forests,
tropical wet evergreen forests, tropical semi-evergreen, tropical moist deciduous, and subtropical hill forests in India (Srivastava 1999; Molur et al.
2005). This study clearly shows 75% of
the gibbons we observed in tropical evergreen forest, ranging from 150 to 800m
in elevation. As this species is largelyfrugivorous, food availability may be a limiting
factor for its distribution versus for a folivorousprimate species (Joseph & Ramachandran2003). The status of gibbons in the
state is not conclusively known. There
are only mentions of their presence or absence from protected and non-protected
areas. There is hardly any quantitative
information on the population estimation of H. hoolockbased on systematic studies in NNP with the lone exception of Chetry et al. (2003) (Table 4). They reported 10 groups of H. hoolock comprising 33 individuals in NNP during the
2002 survey. Choudhury(1990) reported 168 H. hoolock in seven
populations for the state. In
comparison, in other northeastern states Das et al. (2005) reported the
occurrence of H. hoolock populations in Assam
(1994) and Tripura (2003) comprising 1985 and 97 individuals, respectively. H. hoolock are
monogamous, maintain a social network within a group and social proximity with
neighboring groups of the same species (Alfred & Sati 1990). Alfred & Sati (1990) also reported that a
typical family group consists of a mated pair and one to three immature
offspring. We compared our group
composition and group size with Chetry et al. (2003)
for NNP and these data are presented in Table 4. Our group size of 2.5 individuals for 20
groups is closely comparable to other studies conducted in different part of H.hoolock distribution range: 3.2 individuals for
24 groups and 3.4 for seven groups (Tilson 1979), 3.1
for eight groups and 3.0 for 14 groups (Chaudhury1990, 1991) in Assam, 3-3.2 for six to 10 groups (Mukherjee1982), 2.1 for 34 groups (Gupta 1994) in Tripura, 3.0 individual for 42 groups
(Alfred & Sati 1990) in Meghalaya, 3.5 for six groups (Gittins1984), 2.3 for five groups and 2.9 for 15 groups (Ahsan1984, 1994), and 2.9 for 13 groups (Feeroz &
Islam 1992) in Bangladesh.
The
economic status of local people affects the gibbon population and its habitat
directly and indirectly and this has become a major concern for gibbon
conservation. Arunachalamet al. (2004) explained the present inherent dependency of the local people on
forest resources, particularly those settled in peripheral areas and inside NNP
(Table.3). Local people use forest
resources and land for extracting fuelwood, housing
materials, medicinal plants, wild vegetables, and for agricultural
activities. This results in forest
fragmentation and degradation in the form of canopy gaps, and food paucity in
both quantity and quality. In
northeastern India, Bangladesh and Myanmar, most H. hoolockhabitat is fragmented (Molur et al 2005; Walker et
al. 2007). This makes gibbons
particularly vulnerable to hunting and predation by domestic and wild dogs
while moving on forest floor to forage for food, mate, and find safe shelter
(C. Loma, Conservator of Forests, Arunachal Pradesh Forest Department, pers.
comm.). Community hunting for their
flesh and socio-cultural practices by tribal people is one of the major threats
to primate species, including the endangered H. hoolock(Biswas 1970; Solanki &Chutia 2004). Further, the songs of gibbons act as a definite guide for hunters,
allowing them to locate gibbons easily (Gupta et al. 2005). This has resulted in a sharp decline of
gibbon populations in the entire northeast. The majority of gibbon populations
in the northeast are very small and declining (Choudhury1996b; Mukherjee et al. 1991-1992; Molur et al. 2005; Walker et al. 2007) and several
fragmented populations face a high probability of extinction (75%) in the near
future (Molur et al. 2005) due to isolation, decrease
in habitat quality, availability of food and hunting. Gupta et al. (2005) stated that the alarming
changes in gibbon habitat that has taken place in the recent years, in the
ecology and landscape, have brought about a number of changes in the
distribution and population structure of H. hoolockin the species’ range. H. hoolock can be considered a keystone and flagship species,
as it helps in the local health of the forest, is a state animal and is a
tourist attraction.
Recommendations
The
interdependence of primates and the local people on one common resource for
their basic requirements is the main cause for concern. Success in conservation goals would largely
depend on the effectiveness with which this interdependence is lessened.
1.
The present study recommends that human activities should be controlled in NNP
in order to conserve H. hoolock populations.
2.
The population should be monitored at regular intervals to evaluate the success
of the management and conservation actions that have been implemented.
3.
Alternative means of survival of local people should be sought by the state
government particularly by the park authority in order to provide a lasting
solution to the population.
4.
The State Forest Department should launch well developed and planned
agro-forestry and social forestry program specifically designed as per the
requirements of the local people inhabiting in and around the park.
5.
Fragmented, degraded forests and canopy gaps that exist in the gibbon’s
habitats in Namdapha National Park should be restored
by planting of preferred and fast growing food plants.
6.
The population, which requires immediate protection and conservation due to
canopy gaps and lack of food availability, should be located and provided some
alternative means for the movement of gibbons from one fragmented patch to
another like bamboo bridges or rope way bridges which have been successfully
experimented with in the Gibbon Wildlife Sanctuary, Assam to reduce canopy
gaps.
7.
A community education program for local people and a visitor center should be
established. Salient features of
gibbons, such as behavior, ecology, and socio-biology, as well as the
importance of the species to humans, should be highlighted using banners,
posters, and leaflets. These should freely distributedto create awareness of the species.
8.
In line with tiger, lion, elephant and crocodile projects, the government
should also start a Hoolock Gibbon project for the
entire range of the species to determine the present distribution, population
status, evaluate threats and conserve the species.
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