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Jackson, R., & Ahlborn, G. (1989). Snow leopards (Panthera- uncia) in Nepal – home range and movements. National Geographic Research, 5(2), 161–175.
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Johnson, W. E., Dratch, P. A., Martenson, J. S., & O'Brien, S. J. (1996). Resolution of recent radiations within three evolutionary lineages of Felidae using mitochondrial restriction fragment length polymorphism variation. Journal of Mammalian Evolution, 3(2), 97–120.
Abstract: Patterns of mitochondrial restriction fragment length polymorphism (RFLP) variation were used to resolve more recent relationships among the species of the Felidae ocelot lineage, domestic cat lineage, and pantherine lineage. Twenty-five of 28 restriction enzymes revealed site variation in at least 1 of 21 cat species. The ocelot lineage was resolved into three separate sister taxa groups: Geoffroy's cat (Oncifelis geoffroyi) and kodkod (O. guigna), ocelot (Leopardus pardalis) and margay (L. wiedii), and pampas cat (Lynchailurus colocolo) and most of the tigrina samples (Leopardus tigrina). Within the domestic cat lineage, domestic cat (Felis catus), European wild cat (F. silvestris), and African wild cat (F. libyca) formed a monophyletic trichotomy, which was joined with sand cat (F. margarita) to a common ancestor. Jungle cat (F. chaus) and black-footed cat (F. nigripes) mtDNAs diverged earlier than those of the other domestic cat lineage species and are less closely related. Within the pantherine lineage, phylogenetic analysis identified two distinct groups, uniting lion (P. leo) with leopard (P. pardus) and tiger (P. tigris) with snow leopard (P. uncia).
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Kinsel, M. J., Kovarik, P., & Murnane, R. D. (1998). Gastric spiral bacteria in small felids. Journal-of-Zoo-and-Wildlife-Medicine, 29(2), 214–220.
Abstract: Nine small cats, including one bobcat (Felis rufus), one Pallas cat (F. manul), one Canada lynx (F. lynx canadensis), two fishing cats (F. viverrina), two margays (F. wiedii), and two sand cats (F. margarita), necropsied between June 1995 and March 1997 had large numbers of gastric spiral bacteria, whereas five large cats, including one African lion (Panthera leo), two snow leopards (P. uncia), one Siberian tiger (P. tigris altaica), and one jaguar (P. onca), necropsied during the same period had none. All of the spiral organisms from the nine small cats were histologically and ultrastructurally similar. Histologically, the spiral bacteria were 5-14 mum long with five to nine coils per organism and were located both extracellularly within gastric glands and surface mucus, and intracellularly in parietal cells. Spiral bacteria in gastric mucosal scrapings from the Canada lynx, one fishing cat, and the two sand cats were gram negative and had corkscrew-like to tumbling motility when viewed with phase contrast microscopy. The bacteria were 0.5-0.7 mum wide, with a periodicity of 0.65-1.1 mum in all cats. Bipolar sheathed flagella were occasionally observed, and no periplasmic fibrils were seen. The bacteria were extracellular in parietal cell canaliculi and intracellular within parietal cells. Culture of mucosal scrapings from the Canada lynx and sand cats was unsuccessful. Based on morphology, motility, and cellular tropism, the bacteria were probably Helicobacter-like organisms. Although the two margays had moderate lymphoplasmacytic gastritis, the other cats lacked or had only mild gastric lymphoid infiltrates, suggesting that these organisms are either commensals or opportunistic pathogens.
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Kosharev, E. P. (1990). Excerpts from “The snow leopard in Kirgizia”. Snow Line, 8(2), 7–8.
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Oli, M. K. (1996). Seasonal patterns in habitat use of blue sheep Pseudois nayaur (Artiodactyla, Bovidae) in Nepal. Mammalia, 60(2), 187–193.
Abstract: Blue sheep (Pseudois nayaur) are the main prey of the endangered snow leopard (Panthera uncia) as well as an important game species in Nepal. A knowledge of how blue sheep utilize their habitat is essential for the scientific management of the sheep and for the conservation of the snow leopard, but we only have a limited understanding of this aspect of blue sheep ecology. I studied the habitat use pattern of blue sheep by direct observation in the Anna-purna Conservation Area, Nepal where they occur sympatrically with the snow leopard. The sheep used grassland habitats more frequently during pre-parturition (spring) and post-parturition (autumn) than other habitat types, but scrub and grassland habitats were used equally frequently during the rut (winter). The sheep used smooth undulating slopes of medium steepness (<40 degrees) on southerly aspects within the elevation range of 4,200-4,600 m most frequently in all seasons, and there was no evidence of seasonal migration along the elevation gradient. When not in broken landforms (e.g., cliff, landslides), the sheep maintained proximity (less than or equal to 150 m) to such features suggesting their importance as escape cover (i.e., from predators). The use of habitat components by blue sheep appeared to be related to the distribution of foraging areas and escape cover.
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Shi, K., Jun, Z. F. S., Zhigang, D., Riordan, P., & MacDonald, D. (2009). Reconfirmation of snow leopards in Taxkurgan Nature Reserve, Xinjiang, China. Oryx, 43(2), 169–170.
Abstract: China may hold a greater proportion of the global snow leopard Panthera uncia population than any other country, with the area of good quality suitable habitat, estimated at nearly 300,000 km2, comprising .50% of that available across the species' entire range. We can now reconfirm the presence of snow leopard in the Taxkurgan area of Xinjiang Province in north-west China after a period of 20 years.
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Trivedi, P. (2009). Project Snow Leopard: Participatory conservation model for the Indian Himalaya. Mountain Forum Bulletin, Ix(2), 52–54.
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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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Dhungel, S. K. (1982). A glimpse of Sagarmatha: world's highest national park. Tigerpaper, IX(2), 11–14.
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Lyngdoh, S., Shrotriya, S., Goyal, S. P., Clements, H., Hayward, M. W., Habib, B. (2014). Prey Preferences of the Snow Leopard (Panthera uncia): Regional Diet Specificity Holds Global Significance for Conservation. Plos One, 9(2), 1–11.
Abstract: The endangered snow leopard is a large felid that is distributed over 1.83 million km2 globally. Throughout its range it relies on a limited number of prey species in some of the most inhospitable landscapes on the planet where high rates of human persecution exist for both predator and prey. We reviewed 14 published and 11 unpublished studies pertaining to snow leopard diet throughout its range. We calculated prey consumption in terms of frequency of occurrence and biomass consumed based on 1696 analysed scats from throughout the snow leopard’s range. Prey biomass consumed was calculated based on the Ackerman’s linear correction factor. We identified four distinct physiographic and snow leopard prey type zones, using cluster analysis that had unique prey assemblages and had key prey characteristics which supported snow leopard occurrence there. Levin’s index showed the snow leopard had a specialized dietary niche breadth. The main prey of the snow leopard were Siberian ibex (Capra sibrica), blue sheep (Pseudois nayaur), Himalayan tahr (Hemitragus jemlahicus), argali (Ovis ammon) and marmots (Marmota spp). The significantly preferred prey species of snow leopard weighed 5565 kg, while the preferred prey weight range of snow leopard was 36–76 kg with a significant preference for Siberian ibex and blue sheep. Our meta-analysis identified critical dietary resources for snow leopards throughout their distribution and illustrates the importance of understanding regional variation in species ecology; particularly prey species
that have global implications for conservation.
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