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Jafri, R. H., & Shah, F. (1994). The role of education and research in the conservation of snow leopard and its habitat in Northern Pakistan. In J.L.Fox, & D.Jizeng (Eds.), (pp. 273–277). Usa: Islt.
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Maheshwari, A., Sharma, D., Sathyakumar, S. (2013). Snow Leopard (Panthera Uncia) surveys in the Western Himalayas, India. Journal of Ecology and Natural Environmnet, 5(10), 303–309.
Abstract: We conducted surveys above 3000 m elevation in eight protected areas of Uttarakhand and Himachal Pradesh. These surveys provide new information on snow leopard in Uttarakhand on the basis of indirect evidence such as pugmark and scat. Snow leopard evidence (n = 13) were found between 3190 and 4115 m elevation. On an average, scats (n = 09) of snow leopard were found for every 56 km walked and pugmarks (n = 04) for every 126 km walked. Altogether, about 39% of the evidence were found on the hill-slope followed by valley floor (30%), cliff (15%) and 8% from both stream bed and scree slope. Genetic analysis of the scats identified three different individuals by using snow leopard specific primers. Snow leopard-human conflicts were assessed through questionnaire based interviews of shepherds from Govind Pashu Vihar Wildlife Sanctuary, Askot Wildlife Sanctuary and Nanda Devi Biosphere Reserve areas of Uttarakhand. Surveys revealed that livestock depredation (mule, goat and sheep) is the only cause of snow leopard-human conflicts and contributed 36% of the diet of snow leopard. Blue sheep and rodents together comprised 36.4% of the total diet. We found that 68.1% of the surveyed area was used for pastoral activities in Uttarakhand and Himachal Pradesh and 12.3% area was under tourism, defence and developmental activities.
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Miller, D. J., & Jackson, R. (1994). Livestock and Snow Leopards:making room for competing users on the Tibetian Plateau. In J.L.Fox, & D.Jizeng (Eds.), (pp. 315–328). Usa: Islt.
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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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Izold, J. (2008). Snow Leopard Enterprise: a conservation project that saves an endangered species and supports needy families. Anim.Keepers' Forum, 9(5), 359–364.
Abstract: The World Conservation Union listed the snow leopard (Uncia uncia) as endangered in 1974. With as few as 3,500 snow leopards left in the wild, scientists placed the snow leopard on the IUCN Red List of critically endangered species shared by animals such as the giant panda and tiger. In an effort to save the snow leopard from extinction, former zoo employee Helen Freeman founded the Snow Leopard Trust in 1981. The Snow Leopard Trust works to save this elusive cat by incorporating community-based conservation projects. One of these project Leopard Enterprise (SLE), impacts poverty stricken communities in Mongolia, Kyrgyz Republic, and Pakistan. It assists over 300 families in its conservation efforts. The economic incentives provided via SLE have led participating communities not to harm the snow leopard or its prey, and to practice sustainable herding. Since the project began in 1997, the number of snow leopards harmed around the communities' territories has dropped to near zero. Additionally, the annual income of families that utilize the benefits of SLE has increased by 25% to 40%. SLE creates this economic benefit by providing the training and equipment necessary to make desirable products from the wool of herd animals. Snow Leopard Trust then purchases these handicraft items from the local people and them globally. Zoos can expand their conservation efforts by simply offering these items in their gift shops. Woodland Park Zoo (WPZ) was the first zoological institution to sell the products, and WPZ continues to generate revenue from them. SLE is a golden opportunity for zoos to increase revenue, assist poor families, and save an endangered species and fragile ecosystem.
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Oli, M. K., Taylor, I. R., & Rogers, M. K. (1993). Diet of the snow leopard (Panthera uncia) in the Annapurna Conservation Area, Nepal. Journal of Zoology London, 231(3), 365–370.
Abstract: The diet of the snow leopard (Panthera uncia) was studied from 213 scats collected between April 1990 and February 1991 in the Annapurna Conservation Area, Nepal. Seven species of wild and five species of domestic mammals were taken, as well as an unidentified mammal and birds. Blue sheep (Pseudois nayaur) were the most frequently eaten prey. Himalayan marmots (Marmota himalayana) were also important, except in winter when they were hibernating. During winter, snow leopards ate more Royle's pika (Ochotona roylei) and domestic livestock. Yaks were eaten more frequently than other livestock types.
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Bannikov A.G. (1971). Genus Panthera.
Abstract: It gives the description of genus Panthera: lion, tiger, leopard, jaguar and snow leopard. The mountains of Central Asia and South Siberia limit the habitat of snow leopard in the USSR. This species is also distributed in the Himalayas, Tibet, and mountains of Mongolia. In summer, it lives at 3,660 3,970 m above sea level, while in winter, following the ungulates; snow leopard descends to 1,800 m. In the Himalayas, it ascends up to 5,500 m above sea level in summer. In Djungar and Talas Ala-Tau, snow leopard keeps at 600 1,200 m. It takes refuge in caves and cracks of rocks. Snow leopard is mostly active in twilights and night, rarer in daylight, and preys on ungulates, hares, marmots, and others. The coupling period is winter or early spring. A gestation is about 90 days. It has 3 5 cubs in a litter.
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Kashkarov D.N. (1932). Order Carnivora- Carnivores. Family Felidae-Cats.
Abstract: Snow leopard inhabits Tien Shan, Pamir, Bukhara and possibly Kopet-dag, as well as the Altai, Tibet, and northern slopes of the Himalayas. It preys on ibex, wild sheep, roe deer, hare, keklik (partridge), snow-cock and porcupine and sometimes attacks livestock. Snow leopard is not considered a dangerous animal since even being wounded, it would escape from men and could only rush to the attack when deadlocked.
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Prakash, I. (1985). Asian predators of livestock. Parasites, pests and predators.World animal science, B2, 405–410.
Abstract: Outlines the distribution, status and predatory behaviour on livestock of Chinese alligator Alligator sinensis, gharial Gavialis gangeticus and several species of Crocodylus and Python; and of wolf Canis lupus, Asiatic jackal C. aureus, dhole (Indian wild dog) Cuon alpinus, brown bear Ursus arctos, Asiatic black bear Selenarctos thibetanus, striped hyaena Hyaena hyaena, clouded leopard Neofelis nebulosa, leopard (panther) Panthera pardus, tiger P. tigris, lion P. leo, snow leopard P. uncia, other Felidae and Viverridae. -P.J.Jarvis
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Kovshar A.F. (1969). Aksu Jabagly nature reserve.
Abstract: In territory of reserve and surrounding foothills 238 birds, 42 mammals, 9 reptiles, 2 amphibious and 2 fishes are registered. The mammal: argali, wild ibex, roe deer, red deer, a wild boar, snow leopard, steppe cat, a stone marten, ermine, red fox, badger, long-tailed marmot and Menzbier's marmot. Irbis is rare in reserve. Ibexes (numerous spesies) and wild sheep are main prey of the snow leopard. With the beginning of ibexes migration snow leopards follow them.
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Prasad, S. N., Chundawat, R. S., Hunter, D. O., Panwar, H. S., & Rawat, G. S. (1991). Remote sensing snow leopard habitat in the trans-Himalaya of India using spatial models and satellite imagery preliminary results. In G. J. Buhyoff (Ed.), (pp. 519–523).
Abstract: The snow leopard (Panthera uncia) is a flagship species for conservation in the high mountain regions of central Asia. Data on snow leopard predation, habitat conditions and range of main prey species were gathered along with thematic maps of the study area for elevation, snow cover, sighting data, kill data, blue sheep use areas, and vegetation data. These data were entered into a GIS and used to help delineate surface features from a satellite image. Preliminary results show that general physiographic features of snow leopard habitat can be detected using satellite imagery and that GIS cartographic modeling techniques can improve this delineation. -from Authors
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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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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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Rana, B. S. (1997). Distinguishing kills of two large mammalian predators in Spiti Valley Himachal Pradesh. J.Bombay Nat.Hist.Soc, 94(3), 553.
Abstract: The author studied livestock killed by predators in the Spiti Valley, India, to determine what species had killed yaks, horses, donkeys, and other domestic animals. Eleven of the kills examined were made by snow leopards and six by the Tibetan wolf. Wolves were involved in surplus killings, while snow leopards kill as food is needed. lgh
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Ferretti, F., Lovari, S., Minder, I., Pellizzi, B. (2014). Recovery of the snow leopard in Sagarmatha (Mt.Everest) National Park: effects on main prey. European Journal of Wildlife Research, (60), 559–562.
Abstract: Consequences of predation may be particularly
heavy on small populations of herbivores, especially if they
are threatened with extinction. Over the 2006–2010 period, we
documented the effects of the spontaneous return of the endangered
snow leopard on the population of the vulnerable
Himalayan tahr. The study area was an area of central
Himalaya where this cat disappeared c. 40 years before, because
of persecution by man. Snow leopards occurred mainly
in areas close to the core area of tahr distribution. Tahr was the
staple (56.3 %) of snow leopards. After the arrival of this cat,
tahr decreased by more than 2/3 from 2003 to 2010 (mainly
through predation on kids). Subsequently, the density of snow
leopards decreased by 60%from2007 to 2010. The main prey
of snow leopards in Asia (bharal, marmots) were absent in our
study area, forcing snow leopards to specialize on tahr. The
restoration of a complete prey spectrum should be favoured
through reintroductions, to conserve large carnivores and to
reduce exploitation of small populations of herbivores, especially
if threatened.
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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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Kashkarov D.N. (1935). The cat family (Felidae).
Abstract: A taxonomic characteristic of family Felidae is given. A brief description of the origin and distribution of modern Felidae species is provided. Snow leopard (Felis uncia) is noticed to be met in the mountains of Central Asia. It says that though being a rare species, snow leopard, together with leopard and tiger, causes a considerable damage by exterminating large ungulates and sometimes attacking man.
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Oli, M. K., & Rogers, E. M. (1996). Seasonal pattern in group size and population composition of blue sheep in Manang, Nepal. Journal of Wildlife Management, 60(4), 797–801.
Abstract: Blue sheep (Pseudois nayaur) are the principal prey of the endangered snow leopard (Panthera uncia) in the Himalayas and adjacent ranges. We studied group size and population composition of blue sheep in Manang District, Annapurna Conservation Area, Nepal. Overall mean group size was 15.6 (SE = 1.3), but it varied seasonally (P lt 0.001), with significantly smaller groups in winter than in other seasons. Mixed groups were most numerous in all seasons, and there was no evidence of sexual segregation. Yearling sex ratio (93.7 M:100 F) did not vary seasonally, nor did the ratio deviate from parity. Adult sex ratio showed a seasonal pattern favoring males post-parturition but female-biased during the rut and pre-parturition. Seasonal variation in sex-specific mortality is offered as a plausible explanation for the observed pattern in adult sex ratio.
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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.
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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.
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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.
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Vipin, G., T. R., Sharma, V., Kumar, B. K., Gaur, A. (2022). Kleptoparasitic interaction between Snow Leopard Panthera uncia and Red Fox Vulpes vulpes suggested by circumstantial evidence in Pin Valley National Park, India. Journal of Threatened Taxa, 14(10), 21928–21935.
Abstract: In the present study, we describe an interspecific kleptoparasitic interaction between two sympatric mammalian carnivores in the high altitudinal Trans-Himalaya region of Himachal Pradesh, India. The study was based on the inferences drawn from the circumstantial evidence (direct and indirect) noticed in the study area in Pin Valley National Park. The inferences from the analysis of the evidence suggested the interaction between a Snow Leopard Panthera uncia, a Red Fox Vulpes vulpes, and a donkey. The arrangement of evidence in a sequential manner suggested that a donkey was killed by a Snow Leopard and a Red Fox stole the food from the carrion of the Snow Leopard’s prey. The Red Fox was killed by the Snow Leopard, which was caught while stealing. The present study represents an example of kleptoparasitic interaction between the Snow Leopard and the Red Fox. This study also proves that such interactions may cost the life of a kleptoparasite and supports the retaliation behaviour of Snow Leopards.
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