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Chen, P., Gao, Y., Lee, A. T. L., Cering, L., Shi, K., Clark, S. G. (2016). Human–carnivore coexistence in Qomolangma (Mt. Everest) Nature Reserve, China: Patterns and compensation. Biological Conservation, (197), 18–26.
Abstract: Livestock depredation by large carnivores is frequently reported in Qomolangma (Mt. Everest) National Nature Reserve, Tibet Autonomous Region of China. Seeking to minimize conflicts, we assessed depredation patterns and ways to upgrade the compensation program. We gathered 9193 conflict records over 2011–2013 to determine the extent and tempo-spatial patterns of the depredation.Weinterviewed 22 local officials and 94 residents to learn their views on depredations and to assess the adequacy of compensation. Data showed that wolves (Canis lupus), lynx (Lynx lynx), and snowleopards (Panthera uncia)were themajor livestock predators. Total livestock
loss accounted for 1.2% of the entire stockholding (n=846,707) in the region. Wolves and lynx tended to take sheep and goats,whereas snowleopards favored yaks and cattle in relation to their proportional abundance. Predation mostly occurred in March through July. Livestock depredation by all predators when combined was best explained by terrain ruggedness and density of small- and large-bodied livestock. Temporal and spatial predation patterns variedamong carnivores.Most respondents (74%) attributed depredation causes to an increase in carnivore abundance. Only 7% blamed lax livestock herding practice for predation losses. Five percent said that
predation was the result of livestock population increases, while 11% had no idea. The compensation scheme was found to be flawed in all aspects—predation verification, application procedure, compensation standard, operational resource allocation, making payment, and other problems. To enhance management for human–carnivore coexistence, we recommend a problem-oriented, integrated, adaptive approach that targets the complex social context of the conflict and addresses the interconnected functions of decision-making process.
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Fox, J. L., Sinha, S.P., Chundawat, R.S. (1992). Activity patterns and habitat use of ibex in the Himalaya mountains of India. Journal of Mammology, 73(3), 527–534.
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Wolf, M., & Ale, S. (2009). Signs at the Top: Habitat Features Influencing Snow Leopard Uncia Uncia Activity in Sagarmatha National Park, Nepal. Journal of Mammalogy, 90(3), 604–611.
Abstract: We used logistic regression to examine factors that affected the spatial distribution of sign (scrapes, feces, footprints, spray or scent marks, and rubbing sites) in a newly reestablished population of snow leopards (Uncia uncia) in Sagarmatha (Mount Everest) National Park, Nepal. Our results indicate that terrain and human activity were the most important factors determining the spatial distribution of leopard activity, whereas presence of their major prey species (Himalayan tahr [Hemitragus jemlahicus]) had only a moderate effect. This suggests that localities at which these animals are active represent a trade-off between suitable habitat and avoidance of potential risk from anthropogenic origins. However, the influence of prey presence was likely underestimated because of the methodology used, and likely weighed in the trade-off as well.
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Khatiwada, J. R., Chalise, M. K., & Kyes, R. (2007). Survey of Snow Leopard (Uncia uncia) and Blue Sheep (Pseudois nayaur) populations in the Kangchenjunga Conservation Area (KCA), Nepal. Final report.
Abstract: This study was carried out in the Kangchenjunga Conservation Area (KCA), Eastern Nepal from Feb – Nov 2007. We used the Snow Leopard Information Management System, SLIMS (second order survey technique) to determine the relative abundance of snow leopard in the upper part of KCA. Altogether, 36 transects (total length of 15.21 km) were laid down in the major three blocks of KCA. 104 Signs (77 scrapes, 20 feces, 2 Scent mark, 3 Pugmarks and 2 hairs) were recorded. Fixed-point count method was applied for blue sheep from appropriate vantage points. We counted total individual in each herd using 8x42 binocular and 15-60x spotting scope. A total of 43 herds and 1102 individuals were observed in the area. The standard SLIMS questionnaire was conducted to find out relevant information on livestock depredation patterns. Out of 35 households surveyed in KCA, 48% of herders lost livestock due to snow leopards. A total of 21 animals were reportedly lost due to snow leopards from August to September 2007.
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Shrestha, B. (2008). Prey Abundance and Prey Selection by Snow Leopard (uncia uncia) in the Sagarmatha (Mt. Everest) National Park, Nepal.
Abstract: Predators have significant ecological impacts on the region's prey-predator dynamic and community structure through their numbers and prey selection. During April-December 2007, I conducted a research in Sagarmatha (Mt. Everest) National Park (SNP) to: i) explore population status and density of wild prey species; Himalayan tahr, musk deer and game birds, ii) investigate diet of the snow leopard and to estimate prey selection by snow leopard, iii) identify the pattern of livestock depredation by snow leopard, its mitigation, and raise awareness through outreach program, and identify the challenge and opportunities on conservation snow leopard and its co-existence with wild ungulates and the human using the areas of the SNP. Methodology of my research included vantage points and regular monitoring from trails for Himalayan tahr, fixed line transect with belt drive method for musk deer and game birds, and microscopic hair identification in snow leopard's scat to investigate diet of snow leopard and to estimate prey selection. Based on available evidence and witness accounts of snow leopard attack on livestock, the patterns of livestock depredation were assessed. I obtained 201 sighting of Himalayan tahr (1760 individuals) and estimated 293 populations in post-parturient period (April-June), 394 in birth period (July -October) and 195 November- December) in rutting period. In average, ratio of male to females was ranged from 0.34 to 0.79 and ratio of kid to female was 0.21-0.35, and yearling to kid was 0.21- 0.47. The encounter rate for musk deer was 1.06 and density was 17.28/km2. For Himalayan monal, the encounter rate was 2.14 and density was 35.66/km2. I obtained 12 sighting of snow cock comprising 69 individual in Gokyo. The ratio of male to female was 1.18 and young to female was 2.18. Twelve species (8 species of wild and 4 species of domestic livestock) were identified in the 120 snow leopard scats examined. In average, snow leopard predated most frequently on Himalayan tahr and it was detected in 26.5% relative frequency of occurrence while occurred in 36.66% of all scats, then it was followed by musk deer (19.87%), yak (12.65%), cow (12.04%), dog (10.24%), unidentified mammal (3.61%), woolly hare (3.01%), rat sp. (2.4%), unidentified bird sp. (1.8%), pika (1.2%), and shrew (0.6%) (Table 5.8 ). Wild species were present in 58.99% of scats whereas domestic livestock with dog were present in 40.95% of scats. Snow leopard predated most frequently on wildlife species in three seasons; spring (61.62%), autumn (61.11%) and winter (65.51%), and most frequently on domestic species including dog in summer season (54.54%). In term of relative biomass consumed, in average, Himalayan tahr was the most important prey species contributed 26.27% of the biomass consumed. This was followed by yak (22.13%), cow (21.06%), musk deer (11.32%), horse (10.53%), wooly hare (1.09%), rat (0.29%), pika (0.14%) and shrew (0.07%). In average, domestic livestock including dog were contributed more biomass in the diet of snow leopard comprising 60.8% of the biomass consumed whilst the wild life species comprising 39.19%. The annual prey consumption by a snow leopard (based on 2 kg/day) was estimated to be three Himalayan tahr, seven musk deer, five wooly hare, four rat sp., two pika, one shrew and four livestock. In the present study, the highest frequency of attack was found during April to June and lowest to July to November. The day of rainy and cloudy was the more vulnerable to livestock depredation. Snow leopard attacks occurred were the highest at near escape cover such as shrub land and cliff. Both predation pressure on tahr and that on livestock suggest that the development of effective conservation strategies for two threatened species (predator and prey) depends on resolving conflicts between people and predators. Recently, direct control of free – ranging livestock, good husbandry and compensation to shepherds may reduce snow leopard – human conflict. In long term solution, the reintroduction of blue sheep at the higher altitudes could also “buffer” predation on livestock.
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Jackson, R. M., & Ahlborn, G. (1988). Observations on the Ecology of Snow Leopard in West Nepal. In H.Freeman (Ed.), (pp. 65–87). India: Snow Leopard Trust and Wildlife Institute of India.
Abstract: This summary of a four year field study by Jackson and Ahlborn begging in 1982 and concluding in 1985, discusses behaviour, trapping and tracking techniques, home range, activity patterns, prey and habitat and survey methods.
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McCarthy, T., Fuller, T., & Munkhtsog, B. (2005). Movements and activities of snow leopards in Southwestern Mongolia (Vol. 124).
Abstract: Four adult (2M:2F) snow leopards (Uncia uncia) were radio-monitored (VHF; one also via satellite) year-round during 1994-1997 in the Altai Mountains of southwestern Mongolia where prey densities (i.e., ibex, Capra siberica) were relatively low (0.9/km2). Marked animals were more active at night (51%) than during the day (35%). Within the study area, marked leopards showed strong a.nity for steep and rugged terrain, high use of areas rich in ungulate prey, and a.nity for habitat edges. The satellite-monitored leopard moved more than 12 km on 14% of consecutive days monitored. Home ranges determined by standard telemetry techniques overlapped substantially and were at least 13-141 km2in size. However, the satellite-monitored individual apparently ranged over an area of at least 1590 km2, and perhaps over as much as 4500 km2. Since telemetry attempts from the ground were
frequently unsuccessful dx¬ 72%_, we suspect all marked animals likely had large home ranges. Relatively low prey abundance in the area also suggested that home ranges of >500 km2were not unreasonable to expect, though these are >10-fold larger than measured in any other part of snow leopard range. Home ranges of snow leopards may be larger than we suspect in many areas, and thus estimation of snow leopard conservation status must rigorously consider logistical constraints inherent in telemetry studies, and the relative abundance of prey.
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Gripenberg, U. (1982). Comparison of chromosome banding patterns in the snow leopard (Panthera uncial) and in other felids. International Pedigree Book of Snow Leopards, (3).
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