Jinguo, Z. (1994). Case report on vesicular calculus of snow leopard. In J.L.Fox, & D.Jizeng (Eds.), (pp. 209–212). Usa: Islt.
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Novikov, G. A. (1962). Carnivorous mammals of the fauna of the USSR. Ussr: Zool. Inst. Acad. Sci.
Abstract: Brief review of physical characteristics, (skull illustration) ecology and distribution
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Hellstrom, M., Kruger, E., Naslund, J., Bisther, M., Edlund, A., Hernvall, P., Birgersson, V., Augusto, R., Lancaster, M. L. (2023). Capturing environmental DNA in snow tracks of polar bear, Eurasian lynx and snow leopard towards individual identification. Frontiers in Conservation Science, 4(1250996), 1–9.
Abstract: Polar bears (Ursus maritimus), Eurasian lynx (Lynx lynx) and snow leopards (Panthera uncia) are elusive large carnivores inhabiting snow-covered and remote areas. Their effective conservation and management are challenged by inadequate population information, necessitating development of novel data collection methods. Environmental DNA (eDNA) from snow tracks (footprints in snow) has identified species based on mitochondrial DNA, yet its utility for individual-based analyses remains unsolved due to challenges accessing the nuclear genome. We present a protocol for capturing nuclear eDNA from polar bear, Eurasian lynx and snow leopard snow tracks and verify it through genotyping at a selection of microsatellite markers. We successfully retrieved nuclear eDNA from 87.5% (21/24) of wild polar bear snow tracks, 59.1% (26/44) of wild Eurasian lynx snow tracks, and the single snow leopard sampled. We genotyped over half of all wild polar bear samples (54.2%, 13/24) at five loci, and 11% (9/44) of wild lynx samples and the snow leopard at three loci. Genotyping success from Eurasian lynx snow tracks increased to 24% when tracks were collected by trained rather than untrained personnel. Thirteen wild polar bear samples comprised 11 unique genotypes and two identical genotypes; likely representing 12 individual bears, one of which was sampled twice. Snow tracks show promise for use alongside other non-invasive and conventional methods as a reliable source of nuclear DNA for genetic mark-recapture of elusive and threatened mammals. The detailed protocol we present has utility for broadening end user groups and engaging Indigenous and local communities in species monitoring.
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Blomqvist, L. (2003). Captive status of the snow leopard in Europe 2001 (Vol. 8).
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Blomqvist, L. (1989). Captive Snow Leopard Report for 1989. International Zoo News, 265, 5–14.
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Lilin, Z. (1994). Captive rearing of a wild snow leopard cub in the Xining Zoo, China. In J.L.Fox, & D.Jizeng (Eds.), (pp. 177–182). Usa: Islt.
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Wharton, D., & Mainka, S. A. (1994). Captive Management of the Snow Leopard. In J.L.Fox, & D.Jizeng (Eds.), (pp. 135–148). Usa: Islt.
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Qiming, X. (1994). Captive care and management of wild snow leopard cubs at the Chengdu Zoo, China. In J.L.Fox, & D.Jizeng (Eds.), (pp. 187–189). Usa: Islt.
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Flerov K.K. (1935). Capra sibirica, Uncia uncia uncia Erxleben.
Abstract: It describes identification signs of ibex and snow leopard; provides data concerning taxonomy, distribution and behavioral patterns of the both species. Snow leopard inhibits the mountains of Central Asia, Tarbagatai, Altai, Sayans and southward to the Humalayas. In Tajikistan snow leopard is distributed in Pamir, and probably, along alpine strip of the ridges in northern Tajikistan. The sub-species status is not defined. It is known that the same type inhabits the area from the Sayans to Himalayas. Only in Tibet and highlands of Sychuan and Gansu lives a well-marked sub-species Uncia uncia uncioides Hodgson.
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Christiansen, P. (2007). Canine morphology in the larger Felidae: implications for feeding ecology. Biological Journal of the Linnean Society, 91, 573–592.
Abstract: Canine morphology is analysed at seven intervals along the crown in both
anteroposterior and lateromedial perspective in seven species of large felids. The puma and the snow leopard have stout, rather conical canines, whereas those of lions, jaguars, and tigers bear substantial resemblance to each other, reflecting their phylogenetic relationships, and are less conical and large. The canines of the leopard are intermediate in morphology between those of the other species, probably reflecting its more generalized diet. The clouded leopard has very large and blade-like canines, which are different from the other analysed species. Canine bending strengths to estimated bite forces appear to differ less among the species than morphology,indicating that the evolution of canines has been constricted with respect to their strength in failure, probably owing to their being equally important for species fitness. However, the clouded leopard again stands out, having a high estimated bite force and rather weak canines in bending about the anteroposterior as well as lateromedial planes compared to the other species. Canine morphology to some extent reflects differences in killing mode, but also appears to be related to the phylogeny. The marked divergence of the clouded leopard is presently not understood.
Keywords: bite force, canine, clouded leopard, feeding behaviour, felid, Homotherium serum, leopard, Megantereoncultridens, morphology, Neofelis nebulosa, paleontology, Panthera pardus, Panthera tigris, puma, Puma concolor, Smilodon fatalis, Smilodon populator, snow leopard, Uncia uncia
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