Korablev, M. P., Poyarkov, A. D., Karnaukhov, A. S., Zvychaynaya, E. Y., Kuksin, A. N., Malykh, S. V., Istomov, S. V., Spitsyn, S. V., Aleksandrov, D. Y., Hernandez-Blanco, J. A., Munkhtsog, B., Munkhtogtokh, O., Putintsev, N. I., Vereshchagin, A. S., Becmurody, A., Afzunov, S., Rozhnov, V. V. (2021). Large-scale and fine-grain population structure and genetic diversity of snow leopards (Panthera uncia Schreber, 1776) from the northern and western parts of the range with an emphasis on the Russian population. Conservation Genetics, .
Abstract: The snow leopard (Panthera uncia Schreber, 1776) population in Russia and Mongolia is situated at the northern edge of the range, where instability of ecological conditions and of prey availability may serve as prerequisites for demographic instability and, consequently, for reducing the genetic diversity. Moreover, this northern area of the species distribution is connected with the western and central parts by only a few small fragments of potential habitats in the Tian-Shan spurs in China and Kazakhstan. Given this structure of the range, the restriction of gene flow between the northern and other regions of snow leopard distribution can be expected. Under these conditions, data on population genetics would be extremely important for assessment of genetic diversity, population structure and gene flow both at regional and large-scale level. To investigate large-scale and fine-grain population structure and levels of genetic diversity we analyzed 108 snow leopards identified from noninvasively collected scat samples from Russia and Mongolia (the northern part of the range) as well as from Kyrgyzstan and Tajikistan (the western part of the range) using panel of eight polymorphic microsatellites. We found low to moderate levels of genetic diversity in the studied populations. Among local habitats, the highest heterozygosity and allelic richness were recorded in Kyrgyzstan (He = 0.66 ± 0.03, Ho = 0.70 ± 0.04, Ar = 3.17) whereas the lowest diversity was found in a periphery subpopulation in Buryatia Republic of Russia (He = 0.41 ± 0.12, Ho = 0.29 ± 0.05, Ar = 2.33). In general, snow leopards from the western range exhibit greater genetic diversity (He = 0.68 ± 0.04, Ho = 0.66 ± 0.03, Ar = 4.95) compared to those from the northern range (He = 0.60 ± 0.06, Ho = 0.49 ± 0.02, Ar = 4.45). In addition, we have identified signs of fragmentation in the northern habitat, which have led to significant genetic divergence between subpopulations in Russia. Multiple analyses of genetic structure support considerable genetic differentiation between the northern and western range parts, which may testify to subspecies subdivision of snow leopards from these regions. The observed patterns of genetic structure are evidence for delineation of several management units within the studied populations, requiring individual approaches for conservation initiatives, particularly related to translocation events. The causes for the revealed patterns of genetic structure and levels of genetic diversity are discussed.
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Korytin S.A. (1986). Animal's behavior near attractions. Animal's reaction to chasing with dogs. Animal behavior and traps.
Abstract: It describes trophic behavior of the cat family species (lion, tiger, leopard, snow leopard, cheetah, caracal, reed cat, wild cat and domestic cat), their reaction to dog-chasing and behavioral patterns when trapped. Snow leopards (Uncia uncia) sometime eat dead animals. After killing the prey they take it away. Irbis eats the carcass, half-risen on front limbs, beginning from the chest and front limbs or lower part of belly, usually not touching intestines. It eats slowly and spends a lot of time near the carcass and returns to the carcass several times. Known are cases that two snow leopards, or a snow leopard and wolf eating the prey together. Snow leopard usually keeps birds off the carcass. If a man approaches snow leopard normally goes away, sometimes putting up with his close presence. Escaping from dogs, snow leopard was seen to plunge into the river. When trapped, snow leopard rather easily surrenders to man.
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Koshkarev, E. (1997). Has the Snow Leopard Disappeared from Eastern Sayan and Western Hovsogol? In R.Jackson, & A.Ahmad (Eds.), (pp. 96–107). Lahore, Pakistan: Islt.
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Koshkarev, E. (1998). Snow leopard along the border of Russia and Mongolia. Cat News, 28, 12–14.
Abstract: The author discusses the distribution of snow leopards along the border of Russia and Mongolia. The range extension of the leopard indicates their ability to cross desert areas that separate mountain habitats.habitat; range extension; scat analysis; techniques; tracks/tracking | snow leopard
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Kovshar A.F. (1990). The Aksu Jabagly nature reserve.
Abstract: It provides general information about the Aksu Jabagly nature reserve (Kazakhstan), its physico-geographical features, description of flora and fauna. The rarest predator of the nature reserve is snow leopard. Its population is about 10 pairs. Its distribution and behavioral patterns are correlated with its main prey ibex. In the past, snow leopard used to be a common species for the Talas Ala-Tau. Today its number has reduced.
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Kyes, R., & Chalise, M. K. (2005). Assessing the Status of the Snow Leopard Population in Langtang National Park, Nepal.
Abstract: This project is part of an ongoing snow leopard study established in 2003 with support from the ISLT. The study involves a multifaceted approach designed to provide important baseline data on the status of the snow leopard population in Langtang National Park (LNP), Nepal and to generate long-term support and commitment to the conservation of snow leopards in the park. The specific aims include: 1) conducting a population survey of the snow leopards in LNP, focusing on distribution and abundance; 2) assessing the status of prey species populations in the park; and 3) providing educational outreach programs on snow leopard conservation for local school children (K-8) living in the park. During the 2004 study period, snow leopard signs were observed (including pugmarks and scats) although somewhat fewer than in 2003. Similarly, the average herd size of the snow leopards' primary prey species in LNP (the Himalayan thar) was a bit lower than in 2003. There is speculation that the thar populations and the snow leopards may be moving to more remotes areas of the park perhaps in response to increasing pressure from domestic livestock grazing. This possibility is being addressed during the 2005 study period.
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Lepcha, R., & Bhutia, C. (2000). Environmental Education in Sikkim (Vol. xvii). Seattle: Islt.
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Lesnyak A.P. (1984). Cats in Uzbekistan's fur trade.
Abstract: Data of distribution, food, and fur trade of Felidae (North Persian leopard, snow leopard, caracal, Turkestan lynx, manul, Turkestan steppe cat, jungle cat [chaus], sand cat) in Uzbekistan is given. Snow leopard is an object of illegal hunting.
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Lovari, S., Boesi, R., Minder, I., Mucci, N., Randi, E., Dematteis, A., and Ale, S. B. (2009). Restoring a keystone predator may endanger a prey species in a human-altered ecosystem: the return of the snow leopard to Sagarmatha National Park. Animal Conservation, 12, 559–570.
Abstract: Twenty-five years ago, the snow leopard Uncia uncia, an endangered large cat, was eliminated from what is now Sagarmatha National Park (SNP). Heavy hunting pressure depleted that area of most medium-large mammals, before it became a park. After three decades of protection, the cessation of hunting and the recovery of wild ungulate populations, snow leopards have recently returned (four individuals). We have documented the effects of the return of the snow leopard on the population of its main wild prey, the Himalayan tahr Hemitragus jemlahicus, a 'near-threatened' caprin. Signs of snow leopard presence were recorded and scats were collected along a fixed trail (130 km) to assess the presence and food habits of the snow leopard in the Park, from 2004 to 2006. Himalayan tahr, the staple of the diet, had a relative occurrence of 48% in summer and 37% in autumn, compared with the next most frequent prey, musk deer Moschus chrysogaster (summer: 20%; autumn: 15%) and cattle (summer: 15%; autumn: 27%). In early summer, the birth rate of tahr (young-to-female ratio: 0.8-0.9) was high. The decrease of this ratio to 0.1-0.2 in autumn implied that summer predation concentrated on young tahr, eventually altering the population by removing the kid cohort. Small populations of wild Caprinae, for example the Himalayan tahr population in SNP, are sensitive to stochastic predation events and may be led to almost local extinction. If predation on livestock keeps growing, together with the decrease of Himalayan tahr, retaliatory killing of snow leopards by local people may be expected, and the snow leopard could again be at risk of local extinction. Restoration of biodiversity through the return of a large predator has to be monitored carefully, especially in areas affected by humans, where the lack of important environmental components, for example key prey species, may make the return of a predator a challenging event.
Keywords: conservation, food habits, genetics, Hemitragus jemlahicus, Himalayan tahr, management, microsatellite, predation, presence, scat, scat analysis, snow leopard, Uncia uncia
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Lukarevskiy V.S. (2003). Peculiarities of communicative behavior of leopard, irbis, lynx, and caracal.
Abstract: It gives the description of communicative behavioral system (visual, olfactory and vocal elements) for two groups of large Felidae species such as leopard-irbis and lynx-caracal. General and specific behavioral regularities are given.
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