|
Ale S. (2005). Have snow leopards made a comeback to the Everest region of Nepal?.
Abstract: In the 1960s, the endangered snow leopard was locally extirpated from the Sagarmatha (Mt. Everest) region of Nepal. In this Sherpa-inhabited high Himalaya, the flourishing tourism since the ascent of Mt Everest in 1953, has caused both prosperity and adverse impacts, the concern that catalyzed the establishment of Mt. Everest National Park in the region in 1976. In the late 1980s, there were reports that some transient snow leopards may have visited the area from adjoining Tibet, but no biological surveys exist to confirm the status of the cats and their prey. Have snow leopards finally returned to the top of the world? Exploring this question was the main purpose of this research project. We systematically walked altogether 24 sign transects covering over 13 km in length in three valleys, i.e. Namche, Phortse and Gokyo, of the park, and counted several snow leopard signs. The results indicated that snow leopards have made a comeback in the park in response to decades of protective measures, the virtual cessation of hunting and the recovery of the Himalayan tahr which is snow leopard's prey. The average sign density (4.2 signs/km and 2.5 sign sites/km) was comparable to that reported from other parts of the cats' range in the Himalaya. On this basis, we estimated the cat density in the Everest region between 1 to 3 cats per 100 sq km, a figure that was supported by different sets of pugmarks and actual sightings of snow leopards in the 60 km2 sample survey area. In the study area, tahr population had a low reproductive rate (e.g. kids-to-females ratio, 0.1, in Namche). Since predators can influence the size and the structure of prey species populations through mortality and through non-lethal effects or predation risk, snow leopards could have been the cause of the population dynamics of tahr in Sagarmtha, but this study could not confirm this speculation for which further probing may be required.
|
|
|
Alexander, J. S., Gopalswamy, A. M., Shi, K., Riordan, P. (2015). Face Value: Towards Robust Estimates of Snow Leopard Densities. Plos One, .
Abstract: When densities of large carnivores fall below certain thresholds, dramatic ecological effects
can follow, leading to oversimplified ecosystems. Understanding the population status of
such species remains a major challenge as they occur in low densities and their ranges are
wide. This paper describes the use of non-invasive data collection techniques combined
with recent spatial capture-recapture methods to estimate the density of snow leopards
Panthera uncia. It also investigates the influence of environmental and human activity indicators
on their spatial distribution. A total of 60 camera traps were systematically set up during
a three-month period over a 480 km2 study area in Qilianshan National Nature Reserve,
Gansu Province, China. We recorded 76 separate snow leopard captures over 2,906 trapdays,
representing an average capture success of 2.62 captures/100 trap-days. We identified
a total number of 20 unique individuals from photographs and estimated snow leopard
density at 3.31 (SE = 1.01) individuals per 100 km2. Results of our simulation exercise indicate
that our estimates from the Spatial Capture Recapture models were not optimal to
respect to bias and precision (RMSEs for density parameters less or equal to 0.87). Our
results underline the critical challenge in achieving sufficient sample sizes of snow leopard
captures and recaptures. Possible performance improvements are discussed, principally by
optimising effective camera capture and photographic data quality.
|
|
|
Alexander, S., A., Zhang, C., Shi, K., Riordan, P. (2016). A granular view of a snow leopard population using camera traps in Central China. Biological Conservation, (197), 27–31.
Abstract: Successful conservation of the endangered snow leopard (Panthera uncia) relies on the effectiveness of monitoring programmes. We present the results of a 19-month camera trap survey effort, conducted as part of a longterm study of the snow leopard population in Qilianshan National Nature Reserve of Gansu Province, China. Weassessed the minimumnumber of individual snowleopards and population density across different sampling periods using spatial capture–recapture methods. Between 2013–2014, we deployed 34 camera traps across an area of 375 km2, investing a total of 7133 trap-days effort. Weidentified a total number of 17–19 unique individuals
from photographs (10–12 adults, five sub-adults and two cubs). The total number of individuals identified and estimated density varied across sampling periods, between 10–15 individuals and 1.46–3.29 snow leopards per 100 km2 respectively. We demonstrate that snow leopard surveys of limited scale and conducted over short sampling periods only present partial views of a dynamic and transient system.We also underline the challenges in achieving a sufficient sample size of captures and recaptures to assess trends in snow leopard population size and/or density for policy and conservation decision-making
|
|
|
Anonymous. (1994). Resolutions Conservation of Snow Leopard, Seventh International Snow Leopard Symposium. In J.L.Fox, & D.Jizeng (Eds.), (pp. 329–331). Usa: Islt.
|
|
|
Anonymous. (2000). A snow leopard conservation plan for Mongolia.
Abstract: The snow leopard faces multiple threats in the Himalayan region, from habitat degradation, loss of prey, the trade in pelts, parts and live animals, and conflict with humans, primarily pastoralists. Consequently, the populations are considered to be in decline and the species is listed as Endangered in the IUCN's Red List. As a 'flagship' and 'umbrella' species the snow leopard can be a unifying biological feature to raise awareness of its plight and the need for conservation, which will benefit other facets of Himalayan biodiversity as well. Some studies of snow leopards have been conducted in the Himalayan region. But, because of its elusive nature and preference for remote and inaccessible habitat, knowledge of the ecology and behaviour of this mystical montane predator is scant. The available information, however, suggests that snow leopards occur at low densities and large areas of habitat are required to conserve a viable population. Thus, many researchers and conservationists have advocated landscape-scale approaches to conservation within a regional context, rather than focusing on individual protected areas.This regional strategy for WWF's snow leopard conservation program is built on such an approach. The following were identified as important regional issues: 1) international trade in snow leopards and parts; 2) the human-snow leopard conflict; 3) the need for a landscape approach to conservation to provide large spatial areas that can support demographically and ecologically viable snow leopard metapopulations; 4) research on snow leopard ecology to develop long-term, science-based conservation management plans; and 5) regional coordination and dialog. While the issues are regional, the WWF's in the region have developed 5-year strategic actions and activities, using the regional strategies as a touchstone, which will be implemented at national levels. The WWF's will develop proposals based on these strategic actions, with estimated budgets, for use by the network for funding and fund-raising. WWF also recognizes the need to collaborate and coordinate within the network and with other organizations in the region to achieve conservation goals in an efficient manner, and will form a working group to coordinate activities and monitor progress.
|
|
|
Aryal, A. (2009). Final Report On Demography and Causes of Mortality of Blue Sheep (Pseudois nayaur) in Dhorpatan Hunting Reserve in Nepal.
Abstract: A total of 206 individual Blue sheep Pseudois nayaur were estimated in Barse and Phagune blocks of Dhorpatan Hunting Reserve (DHR) and population density was 1.8 Blue sheep/sq.km. There was not significant change in population density from last 4 decades. An average 7 animals/herd (SD-5.5) were classified from twenty nine herds, sheep per herds varying from 1 to 37. Blue sheep has classified into sex ratio on an average 75 male/100females was recorded in study area. The sex ratio was slightly lower but not significantly different from the previous study. Population of Blue sheep was seen stable or not decrease even there was high poaching pressure, the reason may be reducing the number of predators by poison and poaching which has
supported to increase blue sheep population. Because of reducing the predators Wolf Canis lupus, Wild boar population was increasing drastically in high rate and we can observed wild boar above the tree line of DHR. The frequency of occurrence of different prey species in scats of different predators shows that, excluding zero values, the frequencies of different prey species were no significantly different (ö2= 10.3, df = 49, p > 0.05). Most of the scats samples (74%) of Snow leopard, Wolf, Common Leopard, Red fox's cover one prey species while two and three species were present in 18% and 8%, respectively. Barking deer Muntiacus muntjak was the most frequent (18%) of total diet composition of common leopards. Pika Ochotona roylei was the most frequent (28%), and Blue sheep was in second position for diet of snow leopards which cover 21% of total diet composition. 13% of diet covered non-food item such as soil, stones, and vegetable. Pika was most frequent on Wolf and Red fox diet which covered 32% and 30% respectively. There was good positive relationship between the scat density and Blue sheep consumption rate, increasing the scat density, increasing the Blue sheep consumption rate. Blue sheep preference by different predators such as Snow leopard, Common leopard, Wolf and Red fox were 20%, 6%, 13% and 2% of total prey species respectively.
|
|
|
Chetri, M., Odden, M., Sharma, K., Flagstad, O., Wegge, P. (2019). Estimating snow leopard density using fecal DNA in a large landscape in north-central Nepal. Global Ecology and Conservation, (17), 1–8.
Abstract: Although abundance estimates have a strong bearing on the conservation status of a
species, less than 2% of the global snow leopard distribution range has been sampled
systematically, mostly in small survey areas. In order to estimate snow leopard density
across a large landscape, we collected 347 putative snow leopard scats from 246 transects
(490 km) in twenty-six 5 5km sized sampling grid cells within 4393 km2 in Annapurna-
Manaslu, Nepal. From 182 confirmed snow leopard scats, 81 were identified as belonging
to 34 individuals; the remaining were discarded for their low (<0.625) quality index. Using
maximum likelihood based spatial capture recapture analysis, we developed candidate
model sets to test effects of various covariates on density and detection of scats on transects.
The best models described the variation in density as a quadratic function of
elevation and detection as a linear function of topography. The average density estimate of
snow leopards for the area of interest within Nepal was 0.95 (SE 0.19) animals per 100 km2
(0.66e1.41 95% CL) with predicted densities varying between 0.1 and 1.9 in different parts,
thus highlighting the heterogeneity in densities as a function of habitat types. Our density
estimate was low compared to previous estimates from smaller study areas. Probably,
estimates from some of these areas were inflated due to locally high abundances in overlap
zones (hotspots) of neighboring individuals, whose territories probably range far beyond
study area borders. Our results highlight the need for a large-scale approach in snow
leopard monitoring, and we recommend that methodological problems related to spatial
scale are taken into account in future snow leopard research.
|
|
|
Christiansen, P. (2007). Canine morphology in the larger Felidae: implications for feeding ecology. Biological Journal of the Linnean Society, 91, 573–592.
Abstract: Canine morphology is analysed at seven intervals along the crown in both
anteroposterior and lateromedial perspective in seven species of large felids. The puma and the snow leopard have stout, rather conical canines, whereas those of lions, jaguars, and tigers bear substantial resemblance to each other, reflecting their phylogenetic relationships, and are less conical and large. The canines of the leopard are intermediate in morphology between those of the other species, probably reflecting its more generalized diet. The clouded leopard has very large and blade-like canines, which are different from the other analysed species. Canine bending strengths to estimated bite forces appear to differ less among the species than morphology,indicating that the evolution of canines has been constricted with respect to their strength in failure, probably owing to their being equally important for species fitness. However, the clouded leopard again stands out, having a high estimated bite force and rather weak canines in bending about the anteroposterior as well as lateromedial planes compared to the other species. Canine morphology to some extent reflects differences in killing mode, but also appears to be related to the phylogeny. The marked divergence of the clouded leopard is presently not understood.
Keywords: bite force, canine, clouded leopard, feeding behaviour, felid, Homotherium serum, leopard, Megantereoncultridens, morphology, Neofelis nebulosa, paleontology, Panthera pardus, Panthera tigris, puma, Puma concolor, Smilodon fatalis, Smilodon populator, snow leopard, Uncia uncia
|
|
|
Fox, J. L., & Chundawat, R. S. (1995). Wolves in the Transhimalayan region of India: The continued survival of a low-density population. Canadian Circumpolar Institute Occasional Publication No.35; Ecology and conservation of wolves in a changing world, 35, 95–103.
Abstract: Canadian Cirumpolar Institute, University of Alberta, Edmonton, Alberta, Canada/Second North American Symposium on Wolves, Edmonton, Alberta, Canada, August 25-27, 1992
|
|
|
Henschel, P., & Ray, J. (2003). Leopards in African Rainforests: Survey and Monitoring Techniques (Wildlife Conservation Society, Ed.).
Abstract: Monitoring Techniques Forest leopards have never been systematically surveyed in African forests, in spite of their potentially vital ecological role as the sole large mammalian predators in these systems. Because leopards are rarely seen in this habitat, and are difficult to survey using the most common techniques for assessing relative abundances of forest mammals, baseline knowledge of leopard ecology and responses to human disturbance in African forests remain largely unknown. This technical handbook sums up the experience gained during a two-year study of leopards by Philipp Henschel in the Lop‚ Reserve in Gabon, Central Africa, in 2001/2002, supplemented by additional experience from carnivore studies conducted by Justina Ray in southwestern Central African Republic and eastern Congo (Zaire) . The main focus of this effort has been to develop a protocol that can be used by fieldworkers across west and central Africa to estimate leopard densities in various forest types. In developing this manual, Henschel tested several indirect methods to assess leopard numbers in both logged and unlogged forests, with the main effort devoted to testing remote photography survey methods developed for tigers by Karanth (e.g., Karanth 1995, Karanth & Nichols 1998; 2000; 2002), and modifying them for the specific conditions characterizing African forest environments. This handbook summarizes the results of the field testing, and provides recommendations for techniques to assess leopard presence/absence, relative abundance, and densities in African forest sites. We briefly review the suitability of various methods for different study objectives and go into particular detail on remote photography survey methodology, adapting previously developed methods and sampling considerations specifically to the African forest environment. Finally, we briefly discuss how camera trapping may be used as a tool to survey other forest mammals. Developing a survey protocol for African leopards is a necessary first step towards a regional assessment and priority setting exercise targeted at forest leopards, similar to those carried out on large carnivores in Asian and South American forests.
|
|
|
Jackson, R. (2000). Linking Snow Leopard Conservation and People-Wildlife Conflict Resolution, Summary of a multi-country project aimed at developing grass-roots measures to protect the endangered snow leopard from herder retribution. Cat News, 33, 12–15.
|
|
|
Jiang, Z. (2005). Snow leopards in the Dulan International Hunting Ground, Qinghai, China.
Abstract: From March to May, 2006œªwe conducted extensive snow leopard surveys in the Burhanbuda Mountain Kunlun Mountains, Qinghai Province, China. 32 linear transect of 5~15 km each, which running through each vegetation type, were surveyed within the study area. A total of 72 traces of snow leopard were found along 4 transects (12.5% of total transects). The traces included pug marks or footprints, scrapes and urine marks. We estimated the average density of wild ungulates in the region was 2.88ñ0.35 individuals km-2(n=29). We emplaced 16 auto2 trigger cameras in different environments and eight photos of snow leopard were shot by four cameras and the capture rate of snow leopard was 71.4%. The minimum snow leopard population size in the Burhanbuda Mountain was two, because two snow leopards were phototrapped by different cameras at almost same time. Simultaneously, the cameras also shot 63 photos of other wild animals, including five photos are unidentified wild animals, and 20 photos of livestock. We evaluated the human attitudes towards snow leopard by interviewing with 27 Tibetan householders of 30 householders live in the study area. We propose to establish a nature reserve for protecting and managing snow leopards in the region. Snow leopard (Uncia uncia) is considered as a unique species because it lives above the snow line, it is endemic to alpines in Central Asia, inhabiting in 12 countries across Central Asia (Fox, 1992). Snow leopard ranges in alpine areas in Qinghai, Xinjiang, Inner Mongolia, Tibet, Gansu and Sichuan in western China (Liao, 1985, 1986; Zhou, 1987; Ma et al., 2002; Jiang & Xu, 2006). The total population and habitat of snow leopards in China are estimated to be 2,000~2,500 individuals and 1,824,316 km2, only 5% of which is under the protection of nature reserves. The cat's current range is fragmented (Zou & Zheng, 2003). Due to strong human persecutions, populations of snow leopards decreased significantly since the end of the 20th century. Thus, the
snow leopards are under the protection of international and domestic laws. From March to May, 2006, we conducted two field surveys in Zhiyu Village, Dulan County in Burhanbuda Mountain, Kunlun Mountains, China to determine the population, distribution and survival status of snow leopards in the area. The aim of the study was to provide ecologic data for snow leopard conservation.
|
|
|
Koshkarev, E. P. (1992). Range Structure, Numbers and Population Status of the Snow Leopard in the Tien Shan (Vol. x). Seattle: International Snow Leopard Trust.
|
|
|
Li, X., Wei, C., Chen, X., Jia, D., Li, P., Liang, S., Jikmed, A., Gao, Y., Zhao, X., Chu, M., Sharma, K., Alexander, J. A., Lu, Z., Xiao, L. (2025). First large‑scale assessment of snow leopard population in China using existing data from multiple organizations. Biodiversity and Conservation, , 1–17.
Abstract: Abundance estimation of large carnivores is essential for their effective conservation planning, yet estimating population size is challenging due to their elusive and wide-ranging nature. China is estimated to encompass 60% of the snow leopard Panthera uncia habitat, making it a crucial pillar for global snow leopard conservation. However, no large-scale population assessment has been conducted despite scattered survey effort accumulating rapidly in recent years. This study combined and standardized existing camera trap sur-
vey data from 12 sites collected by four organizations during 2015 ~ 2021 to estimate snow leopard population in an area of 360,000 km2 on the Tibetan Plateau, China. The representativeness of existing survey was evaluated based on two habitat stratification approaches to achieve less biased population assessment. Spatially explicit capture-recapture (SECR) models were applied for snow leopard density estimation and the top-ranked model showed a significant positive correlation between conservation priority strata and density. An average snow leopard density of 0.90 /100 km2 (95% CI: 0.68 ~ 1.21 /100 km2) and a population size of 1,002 (95% CI: 755 ~ 1,341) individuals was estimated for the defined snow leopard habitat. Two more conservative estimates of 971 (95% CI: 732 ~ 1,287) and 978 (95% CI: 737 ~ 1,267) individuals were generated within two defined survey regions, in which our data had higher representativity. This study presents a practical approach to synthesize existing population survey data for large-scale population assessments of individually identifiable species. The estimated number represents 11 ~ 21% of the global snow leopard population, indicating high conservation value of this region.
|
|
|
McCarthy, K., Fuller, T., Ming, M., McCarthy, T., Waits, L., & Jumabaev, K. (2008). Assessing Estimators of Snow Leopard Abundance (Vol. 72).
Abstract: The secretive nature of snow leopards (Uncia uncia) makes them difficult to monitor, yet conservation efforts require accurate and precise methods to estimate abundance. We assessed accuracy of Snow Leopard Information Management System (SLIMS) sign surveys by comparing them with 4 methods for estimating snow leopard abundance: predator:prey biomass ratios, capture-recapture density estimation, photo-capture rate, and individual identification through genetic analysis. We recorded snow leopard sign during standardized surveys in the SaryChat Zapovednik, the Jangart hunting reserve, and the Tomur Strictly Protected Area, in the Tien Shan Mountains of Kyrgyzstan and China. During June-December 2005, adjusted sign averaged 46.3 (SaryChat), 94.6 (Jangart), and 150.8 (Tomur) occurrences/km. We used
counts of ibex (Capra ibex) and argali (Ovis ammon) to estimate available prey biomass and subsequent potential snow leopard densities of 8.7 (SaryChat), 1.0 (Jangart), and 1.1 (Tomur) snow leopards/100 km2. Photo capture-recapture density estimates were 0.15 (n = 1 identified individual/1 photo), 0.87 (n = 4/13), and 0.74 (n = 5/6) individuals/100 km2 in SaryChat, Jangart, and Tomur, respectively. Photo-capture rates
(photos/100 trap-nights) were 0.09 (SaryChat), 0.93 (Jangart), and 2.37 (Tomur). Genetic analysis of snow leopard fecal samples provided minimum population sizes of 3 (SaryChat), 5 (Jangart), and 9 (Tomur) snow leopards. These results suggest SLIMS sign surveys may be affected by observer bias and environmental variance. However, when such bias and variation are accounted for, sign surveys indicate relative abundances similar to photo rates and genetic individual identification results. Density or abundance estimates based on capture-recapture or ungulate biomass did not agree with other indices of abundance. Confidence in estimated densities, or even detection of significant changes in abundance of snow leopard, will require more effort and better documentation.
|
|
|
Meiers, S. T. (1992). Habitat use by captive puma (Felis concolor) and snow leopards (Pathera uncia) at the Lincoln Park Zoo, Chicago, Illinois. Ph.D. thesis, DePaul University, .
Abstract: Between May 1990 and January 1991, behavioral observations were made of two captive pumas (Felis concolor Linnaeus), and two captive snow leopards (Panthera uncia Schreber) in their outdoor exhibits at the Lincoln Park Zoological Gardens, Chicago, Illinois. Behaviors compared within and between species included: 1) time spend in the different habitat types; 2) time budgets for the different behaviors: laying, moving, sitting, standing, crouching, in the tree, drinking, urinating, defecating, within their inside dens, and “behavior not determined” when the identity or behavior of the individuals could not be determined; and 3) mobility of the animals within their exhibits. Also examined were: 4) preferences for different habitat types; 5) recommendations for future exhibit designs. Both species located themselves within their exhibits in a non-random manner. The majority of cats' time was spent in elevated locations (i.e., gunite ledges approximately 1-5.5 m above ground-level). Snow leopards exhibited this tendency to a greater extent than did the pumas. Both species also spent the majority of their time in the lying-down behavior; again snow leopards displayed this tendency significantly more than the pumas. Pumas were highly mobile and changed locations and behaviors in their exhibit significantly more than the snow leopards. No significant differences were noted between conspecifics in regard to habitat type preference, or mobility within the exhibit. Suggestions for future exhibit design include elevated locations for the cats to lay and look around within and outside their exhibits, caves for access to shade or relief from inclement weather, and ground surfaces to move about on. Features for exhibit design should take into consideration the natural habitat of the cat to occupy the exhibit.
|
|
|
Ming, M., Chundawat R.S., Jumabay, K., Wu, Y., Aizeizi, Q., & Zhu, M. H. (2006). Camera trapping of snow leopards for the photo capture rate and population size in the Muzat Valley of Tianshan Mountains. Acta Theriologica Sinica, 52(4), 788–793.
Abstract: The main purpose of this work was to study the use of infrared trapping cameras to estimate snow leopard Uncia uncia population size in a specific study area. This is the first time a study of this nature has taken place in China. During 71 days of field work, a total of 36 cameras were set up in five different small vales of the Muzat Valley adjacent to the Tomur Nature Reserve in Xinjiang Province, E80ø35' – 81ø00' and N42ø00' – 42ø10', elevation 2'300 – 3'000 m, from 18th October to 27th December 2005. We expended approximately 2094 trap days and nights total (c. 50'256 hours). At least 32 pictures of snow leopards, 22 pictures of other wild species (e.g. chukor, wild pig, ibex, red fox, cape hare) and 72 pictures of livestock were taken by the passive Cam Trakker (CT) train monitor in about 16 points of the Muzat Valley. The movement distance of snow leopard was 3-10 km/day. And the capture rate or photographic rate of snow leopard was 1.53%. Meanwhile, 20 transects were run and 31 feces sample were collected. According to 32 photos, photographic rate and sign survey after snowing on the spot, were about 5-8 individuals of snow leopards in the research area, and the minimum density of snow leopard in Muzat Valley was 2.0 – 3.2 individuals/100 km2. We observed the behavior of ibex for 77.3 hours, and found about 20 groups and a total of approximately 264 ibexes in the research area.
|
|
|
Ming, M., Munkhtsog, B., Xu, F., Turghan, M., Yin, S. -jing, & Wei, S. - D. (2005). Markings as Indicator of Snow Leopard in Field Survey, in Xinjiang.
Abstract: The Snow Leopard (Uncia uncia) was a very rare species in China. The survey on the markings of Snow Leopard in Ahay and Tianshan Mountains is the major activity of the Project of Snow Leopard in Xinjiang, supported by International Snow Leopard Trust(ISLT)and Xinjiang Conservation Fund(XCF). During the field work from Sep to Nov 2004 the Xinjiang Snow Leopard Group(XSLG) set 67 transects of a total length of 47 776 m with mean transect length is 7 1 3 m at 9 locations.Total of 1 l 8 markings of Snow Leopards were found in 27 transects the mean density is 247km. The markings of Snow Leopard included the pug marks or footprints, scrapes, feces, bloodstain, scent spray, urine, hair or fur, claw rake, remains of prey corpse, sleep site, roar and others. From the quantity and locations of marks the XSLG got the information on habitat selection distribution region and relative abundance of the Snow Leopard in the study areas. The survey also provided knowledge on distribution and abundance of major prey potential conservation problems and human attitudes to Snow Leopards by taking 200 questionnaires in the study areas.
|
|
|
Mishra, C., & Madhusudan, M. D. (2002). An Incentive Scheme for Wildlife Conservation in the Indian Trans-Himalaya.. Islt: Islt.
Abstract: The habitat of the snow leopard Uncia uncia across South and Central Asia is subject to extensive pastoral use. Levels of livestock depredation by the snow leopard and other carnivores in the region are high, and often provokes retaliatory killing by the herders. This direct threat to large carnivores is further aggravated by a depletion of wild prey due to poaching and out-competition by livestock. In this paper, we describe a pilot project in the Indian Trans-Himalaya, which uses an incentive scheme to create areas free from livestock grazing on community-owned land, thereby fostering conservation commitment among local
pastoralists, as well as contributing directly to an enhancement of wild prey density.
|
|
|
Moheb, Z., Rajabi, A. M., Jahed, N., Ostrowski, S., Zahler, P. I., Fuller, T. K. (2022). Using double-observer surveys to monitor urial and ibex populations in the Hindu Kush of Wakhan National Park, Afghanistan. Oryx, , 1–7.
Abstract: We surveyed the urial Ovis vignei and Siberian ibex Capra sibirica in the Hindu Kush mountain range of Wakhan National Park in north-eastern Afghanistan to determine their population status and identify potential drivers of population change. We conducted two double- observer ground surveys, in April–May 2015 and 2018, in 10 areas (total = 288 km2). Urial herds were mostly com- posed of both sexes (78% of observed herds), the mean adult sex ratio (females:males) was 100:70, and the mean female:juvenile ratio was 100:53. In 2018 we calculated a urial density of 35/100 km2, compared to 72/100 km2 in 2015. Ibex herds were mostly (79%) composed of both sexes, the mean adult sex ratio (females:males) was 100:103, and the mean female:juvenile ratio was 100:58. Ibex density estimates were similar in 2015 and 2018 (c. 250/100 km2). We discuss the usefulness of the double-observer methods for ungulate surveys, highlight the value of viewshed calculations and discuss the possible causes of urial population decline. To ensure the conservation of these ungulate populations, we recommend continued regular monitoring, measures to address poaching and research to clarify the taxonomical status of urials in Wakhan.
|
|
|
Oli, M. (1994). Snow leopards and blue sheep in Nepal: Densities and predator: Prey ratio (Vol. 75).
Abstract: I studied snow leopards (Panthera uncia) and blue sheep (Pseudois nayaur) in Manang District, Annapurna Conservation Area, Nepal, to estimate numbers and analyze predatorprey interactions. Five to seven adult leopards used the 105-km2 study area, a density of 4.8 to 6.7 leopards/100 km2. Density of blue sheep was 6.6-10.2 sheep/km2, and biomass density was 304 kg/km2. Estimated relative biomass consumed by snow leopards suggested that blue sheep were the most important prey; marmots (Marmota himalayana) also contributed significantly to the diet of snow leopards. Snow leopards in Manang were estimated to harvest 9-20% of total biomass and 11-24% of total number of blue sheep annually. Snow leopard :blue sheep ratio was 1 :1 14-1 :159 on a weight basis, which was considered sustainable given the importance of small mammals in the leopard's diet and the absence of other competing predators.
|
|
|
Oli, M. K. (1994). Snow leopards and blue sheep in Nepal: Densities and predator: prey ratio. Journal of Mammalogy, 75(4), 998–1004.
Abstract: I studied snow leopards (Panthera uncia) and blue sheep (Pseudois nayaur) in Manang District, Annapurna Conservation Area, Nepal, to estimate numbers and analyze predator-prey interactions. Five to seven adult leopards used the 10-5-km-2 study area, a density of 4.8 to 6.7 leopards/100 km-2. Density of blue sheep was 6.6 10.2 sheep/km-2, and biomass density was 304 kg/km-2. Estimated relative biomass consumed by snow leopards suggested that blue sheep were the most important prey; marmots (Marmota himalayana) also contributed significantly to the diel of snow leopards Snow leopards in Manang were estimated to harvest 9-20% of total biomass and 11-24% of total number of blue sheep annually. Snow leopard: blue sheep ratio was 1:114-1:159 on a weight basis, which was considered sustainable given the importance of small mammals in the leopard's diet and the absence of other competing predators.
|
|
|
Oli, M. K. (1997). Winter home range of snow leopards in Nepal. Mammalia, 61(3), 355–360.
Abstract: Because of their low densities, sparse distribution, elusive behavior, and the precipitous habitat they occupy, snow leopards (Uncia uncia) have been the subject of limited study. This study contributes to that limited database with an investigation of the winter home range of 3 radio-collared snow leopards (2 females and 1 male) in the Annapurna Conservation Area, Nepal. Winter home ranges varied from 13.9-22.3 km2 (x = 19.1). Home ranges overlapped extensively within and between sexes, and an area of 8.1 km2 in the core study site was shared by all three leopards.
|
|
|
Rieger, I. (1982). Breeding ounces, Uncia uncia (Schreber, 1775) in zoological gardens. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 49–50). Helsinki: Helsinki Zoo.
|
|
|
Sharma, M., Khanyari, M., Khara, A., Bijoor, A., Mishra, C., Suryawanshi, K. R. (2024). Can livestock grazing dampen density-dependent fluctuations in wild herbivore populations? Journal of Applied Ecology, , 1–12.
Abstract: 1. Conservation policy for the high mountains of Asia increasingly recognises the need to encompass large multi-use landscapes beyond the protected area network. Due to limited long-term research in this region, our understanding of even fundamental processes, such as factors regulating large mammal populations is poor.
2. Understanding the factors that regulate animal populations, especially those generating cyclicity, is a long-standing problem in ecology. Long-term research across multiple taxa (mainly from Europe and North America) has focussed on the relative roles of food and predation in generating cyclicity in population dynamics. It remains unclear how trophic interactions that are influenced by anthropogenic stressors can affect population dynamics in human-modified landscapes.
3. We present a 10-year study to compare the effects of livestock grazing on density-dependent dynamics in two populations of bharal, Pseudois nayaur, in the Himalayas. We combine this with a mechanistic understanding of whether density dependence in these two sites acts predominantly by affecting adult survival or recruitment. We compared and quantified density dependence in the bharal population by fitting Bayesian Gompertz state-space models.
4. We found evidence for negative density dependence which indicates possible cyclic dynamics in the bharal population of the site (Tabo) with low livestock density. The population dynamics of this site were driven by recruited offspring—with a 2-year density-dependent lag effect—rather than adult survival. In the site with high livestock density (Kibber), this density dependence was not detected. We postulate the potential role of excessive grazing by livestock in affecting offspring recruitment, thereby affecting the bharal population in Kibber.
5. Synthesis and applications: Our results suggest that conservation action to facilitate wild herbivore population recovery, such as the development of protected areas and village reserves, needs to account for density-dependent regulation. Sites with trophy hunting require continuous monitoring to understand the effects of density dependence so that appropriate hunting quotas can be formulated.
|
|