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16 December 2013 Spatial and temporal variation in hornbill densities in Namdapha Tiger Reserve, Arunachal Pradesh, north-east India
Rohit Naniwadekar, Aparajita Datta
Author Affiliations +
Abstract

Asian hornbill populations are declining across their ranges because of hunting and deforestation. Five of the 32 Asian hornbill species occur in north-east India. However, vital information on their abundance from the region remains scanty. Understanding spatiotemporal variation in densities provides crucial information for formulating effective conservation strategies based on species-specific abundance patterns and population trends. We examined spatiotemporal variation in densities of four hornbill species in the Namdapha Tiger Reserve, a site identified as an important site for hornbill conservation in Asia. We collected data through variable-width line transect sampling (effort=842.1 km) in the non-breeding season from 2009-12 to estimate hornbill densities. We had 458 detections of four hornbill species. We have estimated White-throated Brown Hornbill densities (7.9 birds/km2) for the first time throughout its entire range. The mean Rufous-necked Hornbill densities (6.9 birds/km2) were higher than those reported elsewhere. Great (3.9 birds/km2) and Wreathed Hornbill (16.1 birds/km2) densities were comparable with other sites. The peak densities of all hornbill species in November-December are among the highest reported from Asia. Wreathed Hornbill densities showed temporal variation peaking in November-December (68 birds/km2) and drastically declining by March-April (1.3 birds/km2), indicating seasonal altitudinal movement to low-elevation areas outside the reserve during the breeding season. Our results underscored the spatial variation in hornbill distribution, with low densities of Great and the White-throated Brown hornbills in higher elevations. Our study demonstrates the global importance of Namdapha for hornbills, given its large area and high densities of four hornbill species.

Introduction

Asian hornbills (Bucerotidae) are among the largest avian frugivores found in the tropical forests of South and South-east Asia. Hornbills are known to range over large distances [1, 2] and exhibit significant fluctuations over space and time, possibly to track patchily distributed fruiting trees [3]. Given their ability to swallow and regurgitate large seeds unharmed and traverse large distances, hornbills are important dispersers of several large-seeded plants in tropical forests [4]. However, Asian hornbills are hunted for their body parts (casque and tail feathers for traditional attire), for consumption of their meat, and for their body fat, which is believed to have medicinal properties [567]. In addition, they face significant threats from logging [8, 9] and habitat fragmentation [10]. Today, only a third of their natural habitat remains, a large proportion of it in a fragmented state and with extraordinarily high levels of threat to their persistence [4, 11].

As a consequence of these anthropogenic pressures, 34% of the 32 Asian species are listed by IUCN [12] as ‘Near Threatened,’ 19% as ‘Vulnerable,’ 9% as ‘Endangered,’ and 6% as ‘Critically Endangered,’ while only 31% are classified as ‘Least Concern.’ In addition, IUCN [12] lists the population trends of almost 85% of the 32 species as ‘Decreasing.’ Several hornbill species are considered to have been locally exterminated from several sites in their global range [13,14]. Given the declines in hornbill populations throughout their ranges, it is vital to have abundance or density information from sites that are likely to harbor hornbill populations in the long-term. This information will serve as a baseline for monitoring future population trends of hornbill species. Additionally, abundance information is a useful state variable to understand responses of species to natural and anthropogenic disturbances. An understanding of spatial and temporal changes in hornbill densities is useful for identifying areas that are seasonally or spatially important for the different hornbill species, thereby contributing towards devising effective conservation strategies for the different species.

Nine of the 32 species of Asian Hornbills occur in India. Five of these nine hornbill species occur in the tropical and sub-tropical forests of north-east India, where hunting is a major threat to hornbills. These include the Great Buceros bicornis, Rufous-necked Aceros nipalensis, Wreathed Rhyticeros undulatus, White-throated Brown Ptilolaemus austeni and Oriental Pied Hornbill Anthracoceros albirostris. IUCN has classified Rufous-necked Hornbill as ‘Vulnerable’ and Great and White-throated Brown Hornbills as'Near Threatened.’ A few Protected Areas in north-east India have been identified as important sites for hornbill populations [1, 13]. However, information on hornbill densities is available only from two sites in Arunachal Pradesh [14, 15]. Abundances of White-throated Brown Hornbill have not been estimated in India, where its distribution is restricted to eastern Arunachal Pradesh, Nagaland, Mizoram, and eastern Meghalaya in north-east India, although encounter rates for the species were estimated from Namdapha Tiger Reserve [16].

In this study, we present estimates of hornbill densities obtained by sampling in four sessions (years) from 2009 – 2012, with a large sampling effort (total effort = 842.1 km) in Namdapha Tiger Reserve. We also compare densities of four hornbill species in both space (three sampling areas varying in elevational range) and time (between months). These density estimates serve as useful baselines for understanding spatiotemporal variation in densities of four hornbill species, monitoring future population trends, and devising conservation strategies for hornbill species in the landscape. We also highlight the importance of Namdapha Tiger Reserve as a globally significant site for conservation of hornbill species, especially the ‘Vulnerable’ Rufous-necked hornbill.

Methods

Study Area

The study was carried out in Namdapha Tiger Reserve (27°23′30” – 27°39′40″N and 96°15′2” – 96°58′33″E) in Changlang district of Arunachal Pradesh state in north-east India. It is located in the easternmost part of the Eastern Himalaya Biodiversity Hotspot adjoining the Indo-Myanmar Biodiversity Hotspot [17]. The reserve area is 1,985 km2 with elevation ranging from 200 – 4,571 m above sea level. Namdapha Tiger Reserve is contiguous with Kamlang Wildlife Sanctuary to the north, Reserved Forests of Jairampur Forest Division to the south and south-west, and Unclassed State forests of Vijaynagar to the east (Fig. 1a). The Noa Dihing River, tributary of the River Brahmaputra, flows from east to the west of the park.

The reserve harbors the world's northernmost tropical rainforests [18]. The vegetation in the park shows transition from tropical and subtropical broad-leaved forest to pine forests, temperate broad-leaved forests, alpine meadows and perennial snow across the elevation gradient. We conducted this study in the lower elevations (below 1,500 m) of the reserve. Dipterocarpus macrocarpus, Shorea assamica (Dipterocarpaceae), Terminalia myriocarpa (Combretaceae), Altingia excelsa (Hamamelidaceae), Schima wallichi (Theaceae), Beilschmiedia assamica (Lauraceae), Baccaurea sapida (Euphorbiaceae), Castanopsis spp. (Fagaceae) and Saprosma ternatum (Rubiaceae) are the dominant tree species in lower elevations.

Five species of hornbills occur in the reserve: the Great, Rufous-necked, Wreathed, White-throated Brown and the Oriental Pied Hornbill. We sampled mainly in the non-breeding season (November to April). The breeding season of hornbills in Arunachal Pradesh is from March-end to early August [19], while in eastern Arunachal Pradesh, breeding commences only in mid- to late April [16]. We sampled in two phases. We carried out Phase I of the sampling (January 2009 – April 2009, November 2009 -April 2010) in three areas (Hornbill Plateau, Ranijheel area and the 58-75 mile area) (Fig. 1a and Table 1), and Phase II (November 2010 – March 2011, December 2011- February 2012) only on the Hornbill Plateau (Fig. 1b and Table 1). Although Hornbill Plateau and Ranijheel area are approximately 5 km (linear distance) apart, we classify them separately because of elevational differences between the two areas (Table 1). We did not classify the trails into different strata based on elevation because some of the trails, especially in the 58 – 75 mile area, spanned a wide elevation gradient starting from 750 to beyond 1,000 m. Hornbill Plateau, where sampling was carried out in both the phases, covers an area of ~15 km2 near the western border of the Namdapha, north of the Noa Dihing River. The elevation on the Hornbill Plateau ranges from 550 – 810 m. The Ranijheel area is to the east of the Hornbill Plateau. The elevation of the trails in the Ranijheel area ranges from 780 – 1,450 m ASL. The 58 – 75 mile area is to the south of Noa Dihing River and to the east of the Ranijheel area. The elevation in the 58 – 75 mile area ranges from 710 – 1,310 m (Fig 1a). The terrain of the Hornbill Plateau is relatively flat, while in the Ranijheel area, it is more undulating and hilly, and more steep and hilly in the 58 – 75 mile area. We accessed all the sampling sites on foot.

People living in and around Namdapha Tiger Reserve belong to four different tribal communities. There are Lisu settlements outside the eastern border of the park and in some locations inside the park (Fig. 1a). Chakma, Tangsa and Miju Mishmi settlements are outside the western and southwestern boundary of the reserve.

Fig. 1a.

Map of the Namdapha Tiger Reserve showing the three sampling areas (enclosed circle/ellipse) with the trails that were sampled during January 2009 – April 2010 (see Methods section for additional details). The map also shows the different Lisu (local community) settlements inside the Tiger Reserve.

10.1177_194008291300600603-fig1.tif

Fig. 1b

Map focusing on the western portion of the Namdapha Tiger Reserve showing the eight trails that were sampled during November 2010 – February 2012 (see Methods section for additional details) and the Hornbill Camp which served as our base during the period of the study.

10.1177_194008291300600603-fig2.tif

Distance Sampling

We used variable-width line transect surveys for sampling hornbills [20]. One or two observers walked each trail in the mornings (0500 – 1100 hr) and/or in the afternoons (1300 – 1700 hr). The average speed of walk was 1.5 km/hr. We recorded species identity, number of individuals, and the perpendicular distance to the centre of the flock following standard line transect protocol [20]. Distances were measured with a Bushnell Rangefinder (Sport 450).

Phase I

In Phase I, we sampled along nine trails (Fig. 1a and Table 1) including two trails on the Hornbill Plateau, three trails on the Ranijheel area, and four trails in the 58 mile – 75 mile area (Table 1). Two of these trails (Waa-si and 75 mile trail) were sampled only from January till April 2009, due to logistic constraints in accessing the sites regularly. We replaced these two trails by two other trails (58 mile and 61 mile) in the same elevation range for sampling from November 2009 – April 2010. The length of the trails varied from 1.5 – 2 km. In Phase I, the total sampling effort was 470.1 km and the sampling effort along each trail varied from 20 – 86 km (Table 1).

Table 1

Details (elevation, sampling duration, trail length and effort along each trail) of the sampled sites inside Namdapha Tiger Reserve. Sampling in Phase I was carried out from January 2009 – April 2010 and in Phase II was carried out from November 2010 – February 2012.

10.1177_194008291300600603-table1.tif

Phase II

In Phase II, we sampled along eight trails on the Hornbill Plateau (Fig. 1b). The minimum distance between two trails was 500 m, except for two trails that were 300 m apart. Each trail was 1.5 km long. We ensured that no two adjacent trails were walked simultaneously. The total sampling effort during Phase II was 372 km and the total effort along each trail varied from 40.5 – 52.5 km (Table 1).

The total sampling effort for the entire study duration (January 2009 – February 2012) was 842.1 km.

Analysis

Program DISTANCE (ver. 6.0) was used to estimate the densities of four hornbill species [21]. We had only a single detection of the Oriental Pied Hornbill in 842.1 km of sampling effort, which precluded density estimation of this species. We used only direct sightings of perched birds for the DISTANCE analysis. We inspected distance data to detect heaping and outliers. We manually grouped the distance data into intervals for analysis. Sightings were entered as ‘clusters.’ We used size-bias regression (p = 0.15) to control for influences of varying flock sizes on detectability. We used standard combinations of series expansion (half-normal, uniform, hazard-rate) and key functions (cosine, simple polynomial and hermite polynomial) [22]. We compared density estimates of the four hornbill species in 1) the three sampling areas (58-75 mile, Ranijheel area and Hornbill Plateau), and 2) three sampling time (months) intervals (November-December, January-February and March-April). Since we had ≤ 10 trails for the different analyses, we estimated variance by assuming the distribution of the variance estimate as poisson with overdispersion factor 2 [23]. Since we had less than 40 detections in each of the strata in the two analyses (sampling areas and months) for all species, we estimated the detection probability and cluster size by pooling data from all the strata [23]. We estimated the overall density for each hornbill species in the three sampling areas by taking the mean of stratum estimates weighted by the total effort in the stratum.

Results

Overall density estimates

In 842.1 km of total sampling effort, we sighted 79 flocks of Great Hornbill, 188 flocks of Rufous-necked Hornbill, 150 flocks of Wreathed Hornbill and 41 flocks of White-throated Brown Hornbill (Table 2).

The mean flock size varied from 2.3 birds for the Great Hornbill to 8.2 birds for the White-throated Brown Hornbill (Table 3). The detection probability ranged from 0.34 for Great Hornbill to 0.59 for Rufous-necked Hornbill (Table 3). The overall mean density of Wreathed Hornbill was the highest (16.1 birds/km2) followed by White-throated Brown Hornbill (7.9 birds/km2), Rufous-necked Hornbill (6.9 birds/km2) and Great Hornbill (3.9 birds/km2) (Fig. 2, Table 3).

Monthly variation in hornbill densities

Mean Wreathed Hornbill density declined from 68 birds/km2 in November-December to ~ 1 bird/km2 in March-April (Fig. 3; Table 2 and Table 3). Though Great Hornbill density also exhibited fluctuations among months, they continued to be present on the Hornbill Plateau. The mean density of Great Hornbill was lower in January-February (2.1 birds/km2) than in November-December (12.7 birds/km2), but it increased again in March-April (5.4 birds/km2) (Table 3). On the other hand, densities of Rufous-necked and White-throated Brown Hornbill were comparable (Fig. 3; Table 3) among the months (November-December, January-February and March-April).

Table 2

Summary of the total effort (km) and number of detections of the four hornbill species in each of the strata across the different months (monthly variation), and across the three sampling areas (spatial variation).

10.1177_194008291300600603-table2.tif

Spatial variation in hornbill densities

There was considerable variation in hornbill detections among the three study areas (Table 2). In the 58-75 mile area, we did not detect three hornbill species (Great, White-throated Brown and Wreathed Hornbill), while we sighted 23 flocks of Rufous-necked Hornbills there (Table 2). The densities of the Rufous-necked Hornbill were comparable among the three sampling areas (Fig. 4 and Table 3). The mean densities of Great and White-throated Brown Hornbills on the Hornbill Plateau were 5 and 7 times that in the Ranijheel area (Fig. 4 and Table 3). The estimates of Wreathed Hornbill densities were highest on the Hornbill Plateau. We have opportunistically observed Wreathed Hornbills in the 58-75 mile area in the months of November-January.

Fig. 2.

Overall mean (95% CI) densities of the four hornbill species (Great, Rufous-necked, Wreathed and White-throated Brown Hornbill) in Namdapha Tiger Reserve.

10.1177_194008291300600603-fig3.tif

Discussion

Our study demonstrates that Namdapha Tiger Reserve harbours high densities and potentially large populations of four hornbill species, especially the Vulnerable Rufous-necked Hornbill (Fig. 5) and the Near Threatened Great and White-throated Brown Hornbills (Fig. 5) during the non-breeding season from November – April. Wreathed Hornbills (Fig. 5) seasonally visit the area, with densities peaking in months of November and December. The lower elevation forests of the Hornbill Plateau had higher mean densities of the Great and White-throated Brown Hornbills than the higher elevation areas of Ranijheel and the 58-75 mile area.

Table 3

Summary of the mean and 95% Confidence Intervals (CI) of the flock size, detection probability and density of the four hornbill species (Great, Rufous-necked, Wreathed and White-throated Brown Hornbill) across months and sampling areas.

10.1177_194008291300600603-table3.tif

Throughout Asia, only 7% of forests inhabited by hornbills are under Protected Status, and the average size of these Protected Areas is ~ 350 km2[4]. The geographical extent and connectivity with other Protected Areas and forests in India and Myanmar make Namdapha Tiger Reserve one of the most important areas for hornbill conservation in Asia. The mean densities of the Rufous-necked Hornbill in our study areas were almost twice that of Huai Kha Khaeng Wildlife Sanctuary of Thailand (Appendix 1), a site well known for high densities of Rufous-necked Hornbills [24]. Given the high densities of this species (6-8 individuals/km2) throughout the three sampling sites and more than 1,000 km2 of potential habitat (forests below 2,000 m; Fig. 5d), Namdapha harbours a sizeable chunk of the global Rufous-necked Hornbill population. It has been estimated that there has been a 30% decline in the global population size of this species (IUCN 2012). However, based on the results of our study and surveys from Arunachal Pradesh [14], the global population of Rufous-necked Hornbill may need to be revised.

Fig. 3.

Mean (95% CI) monthly densities of the four hornbill species (Great, Rufous-necked, Wreathed and White-throated Brown Hornbill) across the months for all sampling sessions (November-December, January-February and March-April).

10.1177_194008291300600603-fig4.tif

This is the first study to estimate the density of White-throated Brown Hornbill, although there is limited information on the species' presence in other states of north-east India [252627]. Namdapha and the adjoining Kamlang Wildlife Sanctuary are the only two Protected Areas in Arunachal Pradesh where the species occurs. Given 450 km2 of area in Namdapha which is below 1,000 m ASL, Namdapha potentially harbours a sizeable population of this species.

Mean Great Hornbill density in Namdapha was one-third of that in Pakke Tiger Reserve in western Arunachal Pradesh [15], but still comparable to other sites in Western Ghats, India [10] and Thailand [24]. Great hornbill densities are possibly higher in Pakke Tiger Reserve due to the greater extent of suitable lowland forest habitat, high fig and nest tree densities, and better protection.

Fig. 4.

Mean (95% CI) densities of the four hornbill species (Great, Rufous-necked, Wreathed and White-throated Brown Hornbill) across the three sampling areas (58-75 mile area (710-1350 m), Ranijheel area (780-1450 m), Hornbill Plateau (550-810 m).

10.1177_194008291300600603-fig5.tif

The mean densities of Wreathed Hornbills were comparable in Namdapha and Pakke Tiger Reserves and were generally higher than those reported from other studies (Table 3), except in East Kalimantan [Leighton (1982) as cited in 28]. The aptly named Hornbill Plateau had mean combined hornbill densities of 100 individuals/km2 in November-December (Table 3). Apart from two studies [3, 29], which report peak combined densities of 84 individuals/km2 and 82 individuals/km2 from Sulawesi and Borneo respectively, there are no other reports of such high combined densities of hornbills throughout the range of hornbills in Asia, making Namdapha a globally significant site for ensuring long-term conservation of hornbills.

The monthly density of hornbill species on the Hornbill Plateau varied depending on the hornbill species. Wreathed Hornbill densities peaked in November-December and gradually declined until March-April, before the onset of the breeding season. There are no reports of Wreathed Hornbills breeding inside Namdapha [16]. This is also corroborated by information from local tribes. As in other sites, where they are known to breed in the lowland forests [19], they probably breed in the lowland forests in Lohit District in Arunachal Pradesh, Assam or adjoining Myanmar. It is important to identify the breeding sites and the movement routes of the large wintering population of Wreathed Hornbills. Hornbill densities have been documented to fluctuate with food availability [3]. In lowland forests of western Arunachal Pradesh, the density of hornbill food plant trees in the non-breeding season was one-third that of the breeding season [30]. The Wreathed Hornbills seasonally move to the higher elevations during the non-breeding season [30]. We are probably observing a similar pattern in eastern Arunachal Pradesh, where Wreathed Hornbills, which range over much larger areas (> 170 km2) [24, 31], are probably tracking fruits across a wide elevation gradient (~100 m – 2000 m), unlike the Rufous-necked Hornbill and the sedentary White-throated Brown Hornbill, both of which range over much smaller areas (Rufous-necked Hornbill: 25 km2 and White-throated Brown Hornbill: 4.3 – 5.9 km2) [13, 31, 32] and whose monthly densities were comparable. Wreathed hornbills have been recorded in large numbers in the higher elevations of Namdapha (up to 2,000 m) [16, 26]. Our estimates of Wreathed Hornbill densities in the 58-75 mile area are likely to be underestimates, as we were unable to sample during November – December due to logistical constraints.

Great Hornbill density did not exhibit clear trends like the Wreathed Hornbills, but showed monthly fluctuations with highest mean densities in November-December. Like the Wreathed Hornbill, this species is also known to range over large distances (up to 135 km2) [2, 31] probably tracking patchily distributed fruiting figs.

Our study shows that densities of at least two hornbill species (Great and White-throated Brown Hornbill) varied across the elevation gradient (500 – 1450 m) in Namdapha. In north-east India, Great and White-throated Brown Hornbill are common in the lower elevation forests below 1,000 m [8, 15, 16]. The densities of these two species were lower in the higher elevation areas of Ranijheel Plateau and the 58-75 mile area. Since 2003, we have had opportunistic sightings or have heard calls of the Great (seen once and heard twice) and Brown Hornbills (seen on one occasion) in the 58-75 mile area outside distance sampling, indicating that they occur in extreme low densities in this area. The reasons for the absence of these two species from higher areas of Namdapha remain unclear. Densities of Rufous-necked Hornbill were comparable among all the three sampling sites that are spread along a 1,000 m elevation gradient (500-1,450 m). This species is known to prefer the higher elevation areas [1, 13].

Most hornbill species still persist, albeit in lower abundances, outside Protected Areas in Arunachal Pradesh [14]. Protected Areas like the Namdapha Tiger Reserve that harbour hornbill populations at relatively high densities, can potentially serve as a source for adjoining unprotected areas, which experience logging and higher hunting pressures and have low hornbill densities. Given that most hornbill species are highly mobile and range widely, greater abundances of hornbills inside Protected Areas would also result in greater probability of movement of hornbills between forest areas, resulting in greater rates of seed dispersal and potentially enhanced regeneration of degraded nonprotected forests [33].

Fig. 5.

Hornbills of Namdapha Tiger Reserve and aerial views of the forest landscape inside the reserve – a) a male Rufous-necked Hornbill, b) A male White-throated Brown Hornbill, c) Flock of Wreath hornbills. Photo credits: Aparajita Datta, Ramki Sreenivasan/Conservation India and Kalyan Varma.

10.1177_194008291300600603-fig6.tif

Implications for Conservation

Namdapha is among the globally important sites for conservation due to the high densities of the four sympatric hornbill species, including the Rufous-necked Hornbill (Fig. 5), a species considered ‘Vulnerable’ by IUCN. Our study highlights the importance of determining spatial and temporal patterns in abundance of hornbill species, because these data can uncover seasonal movements and highlight the need for protection of lowland sites where breeding of certain species like Wreathed Hornbill likely occurs.

Namdapha is known for its high species richness and biodiversity values and is protected in part by natural barriers due to steep terrain. However, it is a Protected Area that is under varied human pressures, which has resulted in park-people conflict, and is poorly managed [34]. From the late nineties there has been a gradual increase in settlements within Namdapha. Forest patches are being cleared for settlements and paddy cultivation (Fig. 5). There is a need for a resolution of the conflict with the local community and better management to ensure that the forests remain intact and continue to harbour hornbill populations in the future. The area around Namdapha is also undergoing rapid transformation from once-forested habitats to settlements, plantations and degraded forests [35, 36]. In addition, the abundance of most vertebrate groups (especially ungulates, large carnivores) is low due to hunting within the park [37]. Hornbills are the only large vertebrate group that occurs in high densities, possibly because they are not targeted for hunting by the particular tribal groups that access the park. Therefore, the value of the hornbill populations inside Namdapha, especially of the more threatened species like the Rufous-necked and White-throated Brown Hornbill, needs to be highlighted.

Acknowledgements

We thank the Arunachal Pradesh Forest Department and the Field Directors of Namdapha Tiger Reserve for granting us permission to conduct the study. This study was funded by Rufford Small Grants (United Kingdom), Critical Ecosystem Partnership Fund (CEPF) in association with Ashoka Trust for Research in Ecology and the Environment (ATREE) and the International Foundation for Science (Sweden). We are indebted to our Lisu and Tangsa field assistants, especially Akhi Nathany, Ngwayotse Yobin, Duchayeh Yobin and Ngwazakhi Yobin for help in the field. We are indebted to our friends, Japang Pansa and Phupla Singpho and the Namdapha field staff for help and support at Namdapha. We thank Jahnavi Joshi and Ushma Shukla who volunteered for field sampling. We thank Devcharan Jathanna for advice on the finer details of the DISTANCE analysis. R. Raghunath created the maps of the study area. We are grateful to Charudutt Mishra, M. D. Madhusudan, Kavita Isvaran, Jahnavi Joshi, M. O. Anand, Kulbhushansingh Suryavanshi, Rishi Kumar Sharma and Hari Sridhar for useful discussions. We thank Dr. Alejandro Estrada and two anonymous reviewers for useful comments on the manuscript.

References

1.

Kemp, A. C., 1995. The Hornbills. Oxford University Press, Oxford, England. Google Scholar

2.

Keartumsom, Y., Chimchome, V., Poonswad, P., Pattanavibool, A., and Pongpattananurak, N., 2011. Home range of Great Hornbill (Buceros bicornis Linnaeus, 1758) and Wreathed Hornbill (Rhyticeros undulatus (Shaw) 1881) in non-breeding season at Khao Yai National Park, Nakhon Ratchasima Province. Journal of Wildlife in Thailand 18:47–55. Google Scholar

3.

Kinnaird, M. F., O'Brien, T. G., and Suryadi, S., 1996. Population fluctuation in Sulawesi Red-knobbed Hornbills: tracking figs in space and time. Auk 113:431–440. Google Scholar

4.

Kinnaird, M. F., and O'Brien, T. G., 2007. The Ecology and Conservation of Asian Hornbills: Farmers of the Forest. The University of Chicago Press, Chicago, USA. Google Scholar

5.

Bennett, E. L., Nyaoi, A. J., and Sompud, J., 1997. Hornbills Buceros spp. and culture in northern Borneo: can they continue to co-exist. Biological Conservation 82:41–46. Google Scholar

6.

Datta, A., 2002. Status of hornbills and hunting among tribal communities in eastern Arunachal Pradesh. Unpublished Report. Submitted to the Wildlife Conservation Society, New York and WCS-India Program, Bangalore. Google Scholar

7.

Aiyadurai, A., Singh, N. J., and Milner-Gulland, E. J., 2010. Wildlife hunting by indigenous tribes: a case study from Arunachal Pradesh, north-east India. Oryx 44:564–572. Google Scholar

8.

Datta, A., 1998. Hornbill abundance in unlogged forest, selectively logged forest and a forest plantation in Arunachal Pradesh, India. Oryx 32:285–294. Google Scholar

9.

Johns, A. D., 1987. The use of primary and selectively logged rainforest by Malaysian Hornbills (Bucerotidae) and implications for their conservation. Biological Conservation 40:179–190. Google Scholar

10.

Raman, T. R. S., and Mudappa, D., 2003. Correlates of hornbill distribution and abundance in rainforest fragments in the southern Western Ghats. Bird Conservation International 13:199–212. Google Scholar

11.

Laurance, W. F., 1999. Reflections on the tropical deforestation crisis. Biological Conservation 91:109–117. Google Scholar

12.

IUCN. 2012. 2012 IUCN Red List of Threatened Species v. 2012.2. www.iucnredlist.org Google Scholar

13.

Poonswad, P., Kemp, A. C., and Strange, M., 2013. Hornbills of the world: A photographic guide. Draco Publishing and Distributions Pte. Ltd., Singapore and Hornbill Research Foundation, Thailand. Google Scholar

14.

Naniwadekar, R., Mishra, C., Isvaran, K., Madhusudan, M. D., and Datta, A., accepted. Looking beyond parks: Conservation value of ‘unprotected areas’ for hornbills in Arunachal Pradesh, Eastern Himalaya. Oryx. Google Scholar

15.

Dasgupta, S., and Hilaluddin. 2012. Differential effects of hunting on populations of hornbills and imperial pigeons in the rainforests of the Eastern Indian Himalaya. Indian Forester 138:902–909. Google Scholar

16.

Datta, A., 2009. Observations on Rufous-necked Aceros nipalensis and Austen's Brown Anorrhinus austeni Hornbills in Arunachal Pradesh: natural history, conservation status and threats. Indian Birds 5:108–117. Google Scholar

17.

Myers, N., Mittermeier, R. A., Mittermeier, C. G., da Fonseca, G. B. A., and Kent, J., 2000. Biodiversity hotspots for conservation priorities. Nature 403:853–858. Google Scholar

18.

Proctor, J., Haridasan, K., and Smith, G. W., 1998. How far north does lowland evergreen tropical rain forest go? Global Ecology and Biogeography Letters 7:141–146. Google Scholar

19.

Datta, A., and Rawat, G. S., 2004. Nest-site selection and nesting success of three hornbill species in Arunachal Pradesh, north-east India: Buceros bicornis, Aceros undulatus and Anthracoceros albirostris Bird Conservation International 14:249–262. Google Scholar

20.

Buckland, S. T., Anderson, D. R., Burnham, K. P., and Laake, J. L., 2003. Distance sampling: Estimating abundance of biological populations. Chapman and Hall, London. Google Scholar

21.

Thomas, L., Laake, J. L., Rexstad, E. A., Strindberg, S., Marques, F. F. C., Buckland, S. T., Borchers, D. L., Anderson, D. R., Burnham, K. P., Burt, M. L., Hedley, S. L., Pollard, J. H., Bishop, J. R. B., and Marques, T. A., 2009. Distance 6.0 Release 2. Research Unit for Wildlife Population Assessment, University of St. Andrews, UK.  http://www.ruwpa.stand.ac.uk/distance/Google Scholar

22.

Thomas, L., Buckland, S. T., Rexstad, E. A., Laake, J. L., Strindberg, S., Hedley, S. L., Bishop, J. R. B., Marques, T. A., and Burnham, K. P., 2010. Distance software: design and analysis of distance sampling surveys for estimating population size. Journal of Applied Ecology 47:5–14. Google Scholar

23.

Buckland, S. T., Anderson, D. R., Burnham, K. P., Laake, J. L., Borchers, D. L., and Thomas, L., 2001. Introduction to Distance Sampling. Oxford University Press, UK. Google Scholar

24.

Jornburom, P., Chimchome, V., Pattnavibool, A., and Poonswad, P., 2010. Density estimation of hornbills in Huai Kha Khaeng Wildlife Sanctuary, Uthai Thani Province. Thailand Journal of Forestry 29:1–11. Google Scholar

25.

Choudhury, A., 2001. Some bird records from Nagaland, north-east India. Forktail 17:91–103. Google Scholar

26.

Srinivasan, U., Dalvi, S., Naniwadekar, R., Anand, M. O., and Datta, A., 2010. The birds of Namdapha National Park and surrounding areas: recent significant records and a checklist of the species. Forktail 26:92–116. Google Scholar

27.

Ved, N., 2011. Hornbills in southern Mizoram: History, beliefs and recent sightings. Indian Birds 7:117–119. Google Scholar

28.

Gale, G. A., and Thongaree, S., 2006. Density estimates of nine hornbill species in a lowland forest site in Northern Thailand. Bird Conservation International 16:57–69. Google Scholar

29.

Leighton, M., 1982. Fruit resources and patterns of feeding, spacing and grouping among sympatric Bornean hornbills (Bucerotidae). University of California, Davis. Google Scholar

30.

Datta, A., and Rawat, G. S., 2003. Foraging patterns of sympatric hornbills during the nonbreeding season in Arunachal Pradesh, Northeast India. Biotropica 35:208–218. Google Scholar

31.

Poonswad, P., and Tsuji, A., 1994. Ranges of male of the Great Hornbill Buceros bicornis, Brown Hornbill Ptilolaemus tickelli and Wreathed Hornbill Aceros undulatus in Khao Yai National Park, Thailand. Ibis 136:79–86. Google Scholar

32.

Tifong, J., Chimchome, V., Poonswad, P., and Pattnavibool, A., 2007. Home range and habitat use of Rufous-necked Hornbill (Aceros nipalensis) by radio tracking in Huai Kha Khaeng Wildlife Sanctuary, Uthai Thani Province. Thailand Journal of Forestry 26:28–39. Google Scholar

33.

Lenz, J., Fiedler, W., Caprano, T., Friedrichs, W., Gaese, B. H., Wikelski, M., and Bohning-Gaese, K., 2011. Seed-dispersal distributions by trumpeter hornbills in fragmented landscapes. Proceedings of the Royal Society B 278:2257–2264. Google Scholar

34.

Datta, A., 2007. Protecting with people in Namdapha: threatened forests, forgotten people. In: Making Conservation Work: securing biodiversity in this new century. Shahabuddin, G., and Rangarajan, M., (Eds.), pp. 165–209. Permanent Black, New Delhi. Google Scholar

35.

Yadava, R. S., Rao, K. S., and Talukdar, U., 2003. Landuse/landcover change in and around Namdapha National Park in north east India using remote sensing and GIS. Arunachal University Research Journal 6:9–24. Google Scholar

36.

Menon, S., Pontius, R. G.Jr Rose, J., Khan, M. L., and Bawa, K. S., 2001. Identifying conservation-priority areas in the tropics: a land-use change modeling approach. Conservation Biology 15:501–512. Google Scholar

37.

Datta, A., Anand, M. O., and Naniwadekar, R., 2008. Empty forests: Large carnivore and prey abundance in Namdapha National Park, north-east India. Biological Conservation 141:1429–1435. Google Scholar

38.

Mudappa, D., and Raman, T. R. S., 2009. A conservation status survey of hornbills (Bucerotidae) in the Western Ghats, India. Indian Birds 5:90–102. Google Scholar

39.

Chantarat, S., Barrett, C. B., Janvilisri, T., Mudsri, S., Niratisayakul, C., Poonswad, P., 2011. Index insurance for pro-poor conservation of hornbills in Thailand. Proceedings of the National Academy of Sciences 108: 13951–13956. Google Scholar

40.

Poonswad, P., Tsuji, A., Liewviriyakit, R., and Jirawatkavi, N., 1988. Effects of external factors on hornbill breeding and population. In: Proceedings of the 5th World Conference on Breeding Endangered Species in Captivity. Cincinnati Zoo and Botanical Garden, Cincinnati, Ohio, USA. Google Scholar

41.

McConkey, K. R., and Chivers, D. J., 2004. Low mammal and hornbill abundance in the forests of Barito Ulu, Central Kalimantan, Indonesia. Oryx 38:439–447. Google Scholar

42.

Payne, J. C., and Davies, A. G., 1982. A faunal survey of Sabah. WWF Malaysia, Kuala Lumpur, Malaysia. Google Scholar

43.

Anggraini, K., Kinnaird, M. F., and O'Brien, T. G., 2000. The effects of fruit availability and habitat disturbance on an assemblage of Sumatran Hornbills. Bird Conservation International 10:189–202. Google Scholar

Appendices

Appendix 1.

Summary of the mean density estimates of the four hornbill species from several studies across South and South-east Asia. ‘na’ represents data not available due to natural absence of the species at the site or inability to estimate densities due to low sample sizes.

10.1177_194008291300600603-table4.tif
© 2013 Rohit Naniwadekar and Aparajita Datta. This is an open access paper. We use the Creative Commons Attribution 3.0 license http://creativecommons.org/licenses/by/3.0/us/. The license permits any user to download, print out, extract, archive, and distribute the article, so long as appropriate cred it is given to the authors and source of the work. The license ensures that the published article will be as widely available as possible and that your article can be included in any scientific archive. Open Access authors retain the copyrights of their papers. Open access is a property of individual works, not necessarily journals or publishers.
Rohit Naniwadekar and Aparajita Datta "Spatial and temporal variation in hornbill densities in Namdapha Tiger Reserve, Arunachal Pradesh, north-east India," Tropical Conservation Science 6(6), 734-748, (16 December 2013). https://doi.org/10.1177/194008291300600603
Received: 17 July 2013; Accepted: 20 September 2013; Published: 16 December 2013
KEYWORDS
eastern Himalaya
Great Hornbill Buceros bicornis
Rufous-necked Hornbill Aceros nipalensis
White-throated Brown Hornbill Ptilolaemus austeni
Wreathed Hornbill Rhyticeros undulatus
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