Jackson, R., Hunter, D.O. (1995). Snow leopard Survey and conservation handbook (First edition).
Abstract: The objectives of this handbook (First edition) are to provide standard procedures for conducting snow leopard status and distribution surveys; suggest uniform methods for assessing the status and relative abundance of large prey species (ungulates such as blue sheep, argali, markhor, Himalayan tahr, urial, ibex, red deer, and roe deer); offer guidance in evaluating habitat quality and identifying the major environmental factors affecting species welfare; and provide standard forms for reporting the results of these field surveys, and a process for feeding information developed by the International Snow Leopard Trust into Snoe Leopard Information Management System (SLIMS).
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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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Chapron, G. (2005). Re-wilding: other projects help carnivores stay wild. Nature, 437, 318.
Abstract: Letter to Nature Editor, in response to: In their plea for bringing Pleistocene wildlife to the New World (“Re-wilding North America” Nature 436, 913–914; 2005), Josh Donlan and colleagues do not discuss successful efforts to ensure long-term survival of large carnivores in Africa and Asia. A few examples are given.
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Chadwick, D. H. (2008). Out of the Shadows: The elusive Central Asian snow leopard steps into a. National geographic, 213(6), 106–129.
Abstract: The elusive Central Asian snow leopard steps into a risk-filled future.
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Ale, S. B., Boesi, R. (2005). Snow Leopard Sightings on the Top of the World. Cat News, (43), 19–20.
Abstract: Sightings of snow leopards Uncia uncia in the wild are rare. This is because snow leopards occur in low numbers and are very elusive (Schaller 1977). Snow leopards may be sparsely distributed,but they may not, however, be very elusive in the world's highest park, Sagarmatha (Mt. Everest) National Park (86° 30' 53“ E to 86° 99' 08” E and 27° 46' 19“ N to 27° 06' 45” N) in Nepal.
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Zhou, S. (1991). On “uncia uncia” and “meng ji” in Shan Hai Jin (Vol. 13).
Abstract: Meng ji is described in Shan Hui Jin (Classic of Mountains and Rivers) as a leopard-like animal adept in hiding with white fur and a patterned forehead. This article makes a comparison between “meng ji” and “uncia uncia” in terms of their shapes, fur colors, natural environments of habitats, habits, characteristics and native areas, and comes to the conclusion that “meng ji” is what we call “uncia uncia” nowadays. The description of “meng ji” in Shan Hui Jin should be the first record of Uncia uncia in the world.
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Zhang, F., Jiang, Z., Zeng, Y., & McCarthy, T. (2007). Development of primers to characterize the mitochondrial control region of the snow leopard (Uncia uncia) (Vol. 7).
Abstract: The snow leopard (Uncia uncia) is a rare carnivore living above the snow line in central Asia. Using universal primers for the mitochondrial genome control region hypervariable
region 1 (HVR1), we isolated a 411-bp fragment of HVR1 and then designed specific primers
near each end of this sequence in the conserved regions. These primers were shown to yield
good polymerase chain reaction products and to be species specific. Of the 12 snow leopards
studied, there were 11 segregating sites and six haplotypes. An identification case of snow
leopard carcass (confiscated by the police) proved the primers to be a useful tool for forensic
diagnosis in field and population genetics studies.
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Yu, N. Z. C., Wang, X., He, G., Zhang, Z., Zhang, A., Lu, W., et al. (1996). A revision of genus Uncia Gray, 1854 based on mitochondrial DNA restriction site maps. Acta Theriologica Sinica, 16(2), 105–108.
Abstract: The Snow leopard (Panthera uncia) is one of the most threatened wild big cats within its range of distribution, however, the question of its systematic status is a matter of debate. Is it a member of genus Panthera, or is it in its own genus (Uncia)? The analysis of genetic difference at the DNA level may provide useful data to clarify the issue. In the present study, ten hexanucleotide-specific restriction endonucleases were used to evaluate the patterns of mitochondrial DNA variation between the Snow leopard and leopard (P. pardus). The molecular size of mtDNA from the two species was about 16.5 kb. Ten enzymes surveyed 32-34 restriction sites, which corresponded to 192 apprx 204 base pairs, or 1.16% apprx 1.24% of the total mtDNA molecule. A total of 45 restriction sites were mapped; of these sites, twenty-four, which correspond to 53.3% of the total sites, were variable. The sequence divergence between them was 0.075 33, which was undoubtedly in the species-level distinction but did not reach the genus level. Therefore, the Snow leopard should be placed in the genus Panthera rather than in its own ganus. It also seems reasonable to recognize Uncia as a valid subgenus. This conclusion not only support but also supplement the viewpoint of Simpson who treated Uncia as a subgenus within Panthera.
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Yanfa, L. (1985). A preliminary investigation into the geographic distribution of the snow leopard Panthera uncia Schreber. Acta Theriologica Sinica, 5(3), 184–188.
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Xu, F., Ming, M., Yin, S. -jing, & Munkhtsog, B. (2006). Autumn Habitat Selection by Snow Leopard (Uncia uncia) in Beita Mountain, Xinjiang, China.
Abstract: Habitat selection of Snow Leopard ( Unica unica) in Beita Mountain of the Altay Mountain system in northeast Xinjiang was conducted from September to October 2004. Six habitat features of 59 sites used by Snow Leopard and 30 random plots were measured by locating 15 transects surveys in the study area . Vanderploge and Scaviaps selectivity index was used to assess Snow Leopardps selection for the different habitat parameters. Principal Component Analysis was used as the primary factor . The results indicated that Snow Leopard preferred the altitude between 2000 – 2 200 m and avoided 2 600 – 3 000 m ; selected cliff base , ridgeline and avoided hillside and valley bottom ; utilized the shrub and rejected the forest ; selected the nongrazing area and avoided the slightly broken region ; preferred north orientation and rejected the south orientation. The results show that grazing status , vegetation type , topography and the ruggedness are the primary factors for the habitat selection of Snow Leopard.
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