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Fox, J. L., Sinha, S. P., Chundawat, R. S., & Das, P. K. (1991). Status of the snow leopard Panthera uncia in Northwest India. Biological Conservation, 55(3), 283–298.
Abstract: Evidence of snow leopard presence was most abundant in C Ladakh, decreased southward toward the crest of the Himalaya, and was least on the S side of the main Himalaya. Prey populations, primarily blue sheep Pseudois nayaur and Asiatic ibex Capra ibex, were also more plentiful in the areas surveyed to the N of the main Himalaya. Perhaps 400 snow leopard occur throughout NW India. The stronghold of this species in India is apparently the trans- Himalayan ranges in Ladakh where new parks and reserves are being established, some in association with a snow leopard recovery programme of the state of Jammu and Kashmir and a 'Project Snow Leopard' of the central Indian government. Because of the generally low density of snow leopard, conservation measures must also be considered within the large areas of its range lying outside parks and reserves. -from Authors
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Moheb, Z., Fuller, T. K., Zahler, P. I. (2022). Snow Leopard – human conflict as a conservation challenge – a review. Snow Leopard Reports, 1, 11–24.
Abstract: Human conflict with large carnivores continues to be a great conservation challenge, and conflict with snow leopards (Panthera uncia) has been studied to understand causes and propose mitigation schemes. While the nature of snow leopard-human conflict is similar in most cases, reported studies have been case- and area-specific with mitigation strategies not necessarily based on a synthesis of relevant literature. We reviewed snow leopard literature published from 1970-2020 to identify the main drivers of human-snow leopard conflict (HSLC) and describe conservation and conflict mitigation strategies commonly employed. Based on 47 relevant peer-reviewed articles, review papers, book chapters, project reports, and other grey literature, we identified four major conflict domains: livestock management-related, socio-economic/human-related, ecological, and policy-related. Most articles suggested more than one conflict mitigation scheme. Three conflict mitigation domains – preventive, supportive, and compensatory – were widely reflected in the snow leopard-human conflict literature. The most commonly reported mitigation schemes included: 1) building or predator-proofing corrals; 2) training shepherds and improving livestock guarding; 3) livestock insurance schemes; 4) compensation for livestock predation; 5) capacity building, education, and awareness programs; and 6) improved breeding and use of guard dogs. Future management efforts need to tailor their approach depending on cultural, economic, and ecological circumstances.
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Johansson, O., Rauset, G. R., Samelius, G., McCarthy, T., Andren, H., Tumursukh, L., Mishra, C. (2016). Land sharing is essential for snow leopard conservation. Biological Conservation, (203), 1–7.
Abstract: Conserving large carnivores in an increasingly crowded planet raises difficult challenges. A recurring debate is whether large carnivores can be conserved in human used landscapes (land sharing) or whether they require specially designated areas (land sparing). Here we show that 40% of the 170 protected areas in the global range of the snow leopard (Panthera uncia) are smaller than the home range of a single adult male and only 4– 13% are large enough for a 90% probability of containing 15 or more adult females. We used data from 16 snow leopards equipped with GPS collars in the Tost Mountains of South Gobi, Mongolia, to calculate home range size and overlap using three different estimators: minimum convex polygons (MCP), kernel utility distributions (Kernel), and local convex hulls (LoCoH). Local convex hull home ranges were smaller and included lower proportions of unused habitats compared to home ranges based on minimum convex polygons and Kernels. Intra-sexual home range overlapwas low, especially for adult males, suggesting that snowleopards are territorial. Mean home range size based on the LoCoH estimates was 207 km2 ± 63 SD for adult males and 124 km2 ± 41 SD for adult females. Our estimates were 6–44 times larger than earlier estimates based on VHF technology when comparing similar estimators, i.e. MCP. Our study illustrates that protected areas alone will not be able to conserve predatorswith large home ranges and conservationists and managers should not restrict their efforts to land sparing.
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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.
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Xiao, C., Bai, D., Lambert, J. P., Li, Y., Cering, L., Gong, Z., Riordan, P., Shi, K. (2022). How Snow Leopards Share the Same Landscape with Tibetan Agro-pastoral Communities in the Chinese Himalayas. Journal of Resources and Ecology, 13(3), 483–500.
Abstract: The snow leopard (Panthera uncia) inhabits a human-altered alpine landscape and is often tolerated by residents in regions where the dominant religion is Tibetan Buddhism, including in Qomolangma NNR on the northern side of the Chinese Himalayas. Despite these positive attitudes, many decades of rapid economic development and population growth can cause increasing disturbance to the snow leopards, altering their habitat use patterns and ultimately impacting their conservation. We adopted a dynamic landscape ecology perspective and used multi-scale technique and occupancy model to better understand snow leopard habitat use and coexistence with humans in an 825 km2 communal landscape. We ranked eight hypothetical models containing potential natural and anthropogenic drivers of habitat use and compared them between summer and winter seasons within a year. HABITAT was the optimal model in winter, whereas ANTHROPOGENIC INFLUENCE was the top ranking in summer (AICcw≤2). Overall, model performance was better in the winter than in the summer, suggesting that perhaps some latent summer covariates were not measured. Among the individual variables, terrain ruggedness strongly affected snow leopard habitat use in the winter, but not in the summer. Univariate modeling suggested snow leopards prefer to use rugged land in winter with a broad scale (4000 m focal radius) but with a lesser scale in summer (30 m); Snow leopards preferred habitat with a slope of 22° at a scale of 1000 m throughout both seasons, which is possibly correlated with prey occurrence. Furthermore, all covariates mentioned above showed inextricable ties with human activities (presence of settlements and grazing intensity). Our findings show that multiple sources of anthropogenic activity have complex connections with snow leopard habitat use, even under low human density when anthropogenic activities are sparsely distributed across a vast landscape. This study is also valuable for habitat use research in the future, especially regarding covariate selection for finite sample sizes in inaccessible terrain.
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Changxi, X., Bai, D., Lambert, J. P., Li, Y., Cering, L., Gong, Z., Riordan, P., Shi, K. (2022). How Snow Leopards Share the Same Landscape with Tibetan Agro-pastoral Communities in the Chinese Himalayas. Journal of Resources and Ecology, 13(3), 483–500.
Abstract: The snow leopard (Panthera uncia) inhabits a human-altered alpine landscape and is often tolerated by residents in regions where the dominant religion is Tibetan Buddhism, including in Qomolangma NNR on the northern side of the Chinese Himalayas. Despite these positive attitudes, many decades of rapid economic development and population growth can cause increasing disturbance to the snow leopards, altering their habitat use patterns and ultimately impacting their conservation. We adopted a dynamic landscape ecology perspective and used multi-scale technique and occupancy model to better understand snow leopard habitat use and coexistence with humans in an 825 km2 communal landscape. We ranked eight hypothetical models containing potential natural and anthropogenic drivers of habitat use and compared them between summer and winter seasons within a year. HABITAT was the optimal model in winter, whereas ANTHROPOGENIC INFLUENCE was the top ranking in summer (AICcw≤2). Overall, model performance was better in the winter than in the summer, suggesting that perhaps some latent summer covariates were not measured. Among the individual variables, terrain ruggedness strongly affected snow leopard habitat use in the winter, but not in the summer. Univariate modeling suggested snow leopards prefer to use rugged land in winter with a broad scale (4000 m focal radius) but with a lesser scale in summer (30 m); Snow leopards preferred habitat with a slope of 22° at a scale of 1000 m throughout both seasons, which is possibly correlated with prey occurrence. Furthermore, all covariates mentioned above showed inextricable ties with human activities (presence of settlements and grazing intensity). Our findings show that multiple sources of anthropogenic activity have complex connections with snow leopard habitat use, even under low human density when anthropogenic activities are sparsely distributed across a vast landscape. This study is also valuable for habitat use research in the future, especially regarding covariate selection for finite sample sizes in inaccessible terrain.
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Rashid, W., Shi, J., Rahim, I. U., Qasim, M., Baloch, M. N., Bohnett, E., Yang, F., Khan, I., Ahmad, B. (2021). Modelling Potential Distribution of Snow Leopards in Pamir, Northern Pakistan: Implications for Human–Snow Leopard Conflicts. Sustainability, 13(13229), 1–15.
Abstract: The snow leopard (Panthera uncia) is a cryptic and rare big cat inhabiting Asia’s remote and harsh elevated areas. Its population has decreased across the globe for various reasons, includ
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Johansson, O., McCarthy, T., Samelius, G., Andren, H., Tumursukh, L., Mishra, C. (2015). Snow leopard predation in a livestock dominated landscape in Mongolia. Biological Conservation, 184, 251–258.
Abstract: Livestock predation is an important cause of endangerment of the snow leopard (Panthera uncia) across
its range. Yet, detailed information on individual and spatio-temporal variation in predation patterns of
snow leopards and their kill rates of livestock and wild ungulates are lacking.
We collared 19 snow leopards in the Tost Mountains, Mongolia, and searched clusters of GPS positions
to identify prey remains and estimate kill rate and prey choice.
Snow leopards killed, on average, one ungulate every 8 days, which included more wild prey (73%) than
livestock (27%), despite livestock abundance being at least one order of magnitude higher. Predation on
herded livestock occurred mainly on stragglers and in rugged areas where animals are out of sight of herders.
The two wild ungulates, ibex (Capra ibex) and argali (Ovis ammon), were killed in proportion to their
relative abundance. Predation patterns changed with spatial (wild ungulates) and seasonal (livestock)
changes in prey abundance. Adult male snow leopards killed larger prey and 2–6 times more livestock
compared to females and young males. Kill rates were considerably higher than previous scat-based estimates, and kill rates of females were higher than kill rates of males. We suggest that (i) snow leopards
prey largely on wild ungulates and kill livestock opportunistically, (ii) retaliatory killing by livestock herders
is likely to cause greater mortality of adult male snow leopards compared to females and young
males, and (iii) total off-take of prey by a snow leopard population is likely to be much higher than previous
estimates suggest.
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Manati, A. R. (2008). Fur trade of large cats and the question of the subspecies status of leopards in Afghanistan (Der Handel mit Fellen von Grosskatzen und die Abklärung der Unterartenfrage beim. Germany: University of Köln.
Abstract: Over a time of four years the bazars of Afghanistan were surveyed for furs of spotted wild cats, in particular leopards and snow leopards. In 2004 in Kabul a total of 28 furs of leopards were purchased by shopkeepers and 21 sold at an average price of 825 $. In the same year 25 furs of snow leopards were purchased and 19 sold to clients at an average price of 583 $. In 2006 at a single inspection double as many furs of leopards were found to be offered for sale in comparison to the whole year of 2004. Also prices had increased over the two years by 20 % to an average of 1037 $. Similarly the number of furs of snow leopards at 21 pieces was higher than in 2004, and the prices had increased to an average of 652 $. In 2007 investigations rendered more difficult, because the authorities had started to control the fur trade, and the results are not unequivocal. Clients were without any exception foreigners.
Surveys in 2004 in Mazar-e-Sharif, Kunduz, Takhar and Faiz Abad, in 2006 additionally in Baharak and Iskashem in the province of Badakhshan, revealed a regular trade in furs of spotted cats, however not as extensive as in Kabul. The most interesting finding was a fur of a cheetah in Mazar-e-Sharif, the first record of this species after 35 years.
From the surveys can be concluded that leopards still exist in the whole range of its distribution area in Afghanistan. However they don't allow any conclusion on the population size and its threat by hunting. In contrast to the leopard there exists a recent estimation of the population size of the snow leopard, saying that there are still 100 to 200 snow leopards living in Afghanistan. On the basis of these figures as well as the numbers of furs traded annually a Population and Habitat Viability Analysis was conducted. The result of this analysis is alarming. It has to be assumed that the snow leopard will be extinct in Afghanistan within the next ten years. To improve the protection of spotted cats in Afghanistan it needs both, a better implementation of the existing legislation as well as an awareness campaign among potential clients, i. e. foreigners living in Afghanistan.
The second part of this thesis deals with the question of subspecies of leopards in Afghanistan. Out of the 27 subspecies described four are believed to exist in Afghanistan. However, according to a molecularbiological revision of the species there occurs only one subspecies in Afghanistan, Panthera pardus saxicolor. To clarify the subspecies question various measures of furs had been taken in the bazars. The results revealed that the leopards in Afghanistan are the biggest of its species. However a further differentiation according to the area of origin within the country was not possible. Also the traditional differentiation on the basis of colours and patterns on the furs was not possible.
In contrast to the molecularbiological investigations published not only samples of zoo animals were available in this study but also samples from the wild. The own results confim that almost all leopards from Afghanistan and Iran belong to one and the same subspecies, P. p. saxicolor. Only in the most eastern part of Afghanistan, the Indian leopard, Panthera pardus fusca, can be found. The International Studbook for the Persian Leopard was analysed. The whole population derives from a few founder animals, which were imported in the midth fifties from Iran and in the late sixties from Afghanistan. To avoid inbreeding later on the Iranian and the Afghan lines were mixed. A female imported in 1968 from Kabul to Cologne is represented in each of the more than 100 today living animals.Mixing the two lines subsequently is justified by the genetic results of this study. Recently acquired animals from the Caucasus, however, should be tested genetically before integrating them into the zoo population.
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Poyarkov, A. D., Munkhtsog, B., Korablev, M. P., Kuksin, A. N., Alexandrov, D. Y., Chistopolova, M. D., Hernandez-Blanco, J. A., Munkhtogtokh, O., Karnaukhov, A. S., Lkhamsuren, N., Bayaraa, M., Jackson, R. M., Maheshwari, A., Rozhnov, V. V. (2020). Assurance of the existence of a trans-boundary population of the snow leopard (Panthera uncia) at Tsagaanshuvuut – Tsagan- Shibetu SPA at the Mongolia-Russia border. Integrative Zoology, (15), 224–231.
Abstract: The existence of a trans-boundary population of the snow leopard (Panthera uncia) that inhabits the massifs of Tsagaanshuvuut (Mongolia) – Tsagan-Shibetu (Russia) was determined through non-invasive genetic analysis of scat samples and by studying the structure of territory use by a collared female individual. The genetic analysis included species identification of samples through sequencing of a fragment of the cytochrome b gene and individual identification using a panel of 8 microsatellites. The home range of a female snow leopard marked with a satellite Global Positioning System (GPS) collar was represented by the minimum convex polygon method (MCP) 100, the MCP 95 method and the fixed kernel 95 method. The results revealed insignificant genetic differentiation between snow leopards that inhabit both massifs (minimal fixation index [FST]), and the data testify to the unity of the cross-border group. Moreover, 5 common individuals were identified from Mongolian and Russian territories. This finding clearly shows that their home range includes territories of both countries. In addition, regular movement of a collared snow leopard in Mongolia and Russia confirmed the existence of a cross-border snow leopard group. These data support that trans-boundary conservation is important for snow leopards in both countries. We conclude that it is crucial for Russia to study the northern range of snow leopards in Asia.
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