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Ale, S. B., Brown, J.S. (2009). Prey behavior leads to predator: a case study of the Himalayan tahr and the snow leopard in Sagarmatha (Mt. Everest) National Park, Nepal. Israel Journal of Ecology & Evolution, 55(4), 315–327.
Abstract: Rare, elusive predators offer few sightings, hindering research with small sample sizes and lack of experimentation. While predators may be elusive, their prey are more readily observed. Prey respond to the presence of a predator, and these fear responses may have population- and community-level consequences. Anti-predator behaviors, such as vigilance, allow us to sidestep the difficulty of direct field studies of large predators by studying them indirectly. Here we used a behavioral indicator, the vigilance behavior of the Himalayan tahr, the snow leopard’s main local prey, to reveal the distribution and habitat use of snow leopards in the Mt. Everest region of Nepal. We combined techniques of conventional field biology with concepts of foraging theory to study prey behavior in order to obtain insights into the predator’s ecology. The Himalayan tahr’s vigilance behavior correlates with the distribution of snow leopard signs. Tahr actually led us to six sightings of snow leopards. We conclude that behavioral indicators provided by prey offer a valuable tool for studying and monitoring stealthy and rare carnivores.
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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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Sokolov G.A. (2003). Predatory mammals of Central Siberia, status of populations, influence of anthropogenic factors.
Abstract: The species resources of Siberia's fauna decrease from south to north. The highest diversity of species is observed in the mountain systems, the lowest in sub-zones of south and central taiga and steppe zone, where the cat family species are absent. During the last 50 150 years number of species has decreased two- to tenfold. Imperfect hunting management, farming, and mining operations resulted in transformation of the animal habitats. Population of fox, polecat, and sable has reduced; snow leopard and dhole becoming endangered species. If current tendencies continue to develop some species will disappear in the region in decades to come.
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Voronov A.G. (1985). Predatory mammals.
Abstract: Predatory mammal in mountains are submitted by widely widespread species, such, as wolves, to a lynx and bears, and characteristic species for the high mountains, well adapted to mountain conditions and not going down below Alpine zone (a snow leopard, or irbis, occupying mountains of the Central Asia, etc.).
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Ferretti, F., Lovari, S. (2016). Predation may counteract climatic change as a driving force for movements of mountain ungulates.
Abstract: Temperature variations are expected to influence altitudinal movements of mountain herbivores and, in
turn, those of their predators, but relevant information is scarce. We evaluated monthly relationships
between temperature and altitude used by a large mountain-dwelling herbivore, the Himalayan tahr
Hemitragus jemlahicus, and its main predator, the snow leopard Panthera uncia, in an area of central
Himalaya for five consecutive years (2006–2010). In contrast to expectations, there was no significant
direct relationship between altitude of tahr sightings and temperature. The mean altitude of tahr sightings
decreased by c. 200 m throughout our study. As expected, snow leopard movements tracked those of tahr,
although the core area of the snow leopard did not move downwards. Tahr remained the staple of the
snow leopard diet: we suggest that the former did not move upwards in reaction to higher temperature
to avoid encounters with the latter. Avoidance of competition with the larger common leopard Panthera
pardus at lower altitudes could explain why snow leopards did not shift their core area downwards.
Apparently, interspecific interactions (predation; competition) influenced movements of Himalayan tahr
and snow leopards more than climatic variations.
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Fuller, S., & Ahmed, J. (1997). Opportunities for Transfrontier Protected Areas in Northern Pakistan. In R.Jackson, & A.Ashiq (Eds.), (pp. 204–215). Lahore, Pakistan: Islt.
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Schaller, G. B., & Mirza, Z. B. (1971). On the behaviour of Kashmir Markhor (Capra falconeri cashmiriensis). Mammalia, 35, 548–566.
Abstract: Notes snow leopard as main predator in Pakistan study area. Describes content of some snow leopard droppings
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Schaller, G. B. (1972). On the behaviour of Blue Sheep (Pseudois nayaur). Journal of Bombay Natural Historical Society, 69, 523–537.
Abstract: Two or three snow leopards hunted in the study area in eastern Nepal. Describes content of some snow leopard scat
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Tserendeleg, J. (1994). On Protection and Survey of Snow Leopards in Mongolia. In J.L.Fox, & D.Jizeng (Eds.), (pp. 43–46). Usa: Islt.
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Shah, K. B. (1989). On a hunting pair of snow leopards in western Nepal. Journal of Bombay Natural Historical Society, 86, 236–237.
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