Bajimaya, S. (2001). Snow leopard manual: field study techniques for the kingdom of Nepal. Kathmandu, Nepal: WWF Nepal Program.
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Karmacharya, D. (2011). Field Protocol – Scat Collection for Genetic Analysis.
Abstract: Project funded by Snow Leopard Conservation Grant Program. Center for Molecular Genetics, Nepal.
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Kashkarov D.N. (1935). The cat family (Felidae).
Abstract: A taxonomic characteristic of family Felidae is given. A brief description of the origin and distribution of modern Felidae species is provided. Snow leopard (Felis uncia) is noticed to be met in the mountains of Central Asia. It says that though being a rare species, snow leopard, together with leopard and tiger, causes a considerable damage by exterminating large ungulates and sometimes attacking man.
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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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Zong-Yi, W., & Sung, W. (1986). Distribution and recent status of the Felidae in China. In D.S.Miller, &.D.D.Everett (Eds.), (pp. 201–209).
Abstract: Thirteen of the 37 existing species of the family Felidae have been recorded in China. These species are widely distributed throughout the country and inhabit a variety of life zones. Over the past several decades, the populations of most species of cats in China have declined due to overharvest and habitat destruction. China has a Protected Wildlife Species List which was initiated in 1962. Some cat species in China are now endangered or may already be extinct while other species or subspecies are threatened. The authors use limited data on the distribution of cats in China to summarize the staus of each species and the problems facing each. Recomendations for new measures to protect cats in China are made.
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Roth, T. L., Swanson, W. F., Wildt, D. E., Collins, D., Burton, M., & Garell, D. M. (1996). Snow leopard (Panthera uncia) spermatozoa are sensitive to alkaline pH, but motility in vitro is not influenced by protein or energy supplements (Vol. 17).
Abstract: To better understand the biology of snow leopard spermatozoa and to facilitate developing assisted reproduction, a series of studies was conducted to: 1) identify the component(s) of complex culture media responsible for the detrimental effect on sperm survival in vitro, 2) optimize medium for supporting sperm viability, and 3) evaluate sperm capacitation in vitro. Constituents of complex media were added systematically to phosphate-buffered saline (PBS) to isolate the factor(s) influencing snow leopard sperm motility in vitro. Sperm capacitation was also assessed following incubation in PBS with bovine serum albumin (BSA), fetal calf serum (FCS), or heparin. For maintaining sperm motility, there was no benefit (P ? 0.05) to supplementing PBS with low (5%) or high (20%) concentrations of snow leopard serum (SLS) versus FCS or BSA. Likewise, adding supplemental energy substrates (pyruvate, glucose, lactate, or glutamine) did not enhance or hinder (P ? 0.05) sperm motility. However, motility rapidly decreased (P < 0.05) with the addition of NaHCO3 to PBS or Ham's F10 nutrient mixture. Surprisingly, Ham's F10 with no buffering component or with both NaHCO3 and N-Z-hydroxyethylpiperazine-N'-2- ethanesulfonic acid (HEPES) maintained sperm motility at levels similar (P ? 0.05) to PBS. Although sperm motility in all treatments decreased with time, there was a strong inverse relationship (P < 0.01; r = 0.90) between motility and sample pH at 6 hours. Spermatozoa incubated in PBS containing FCS, BSA, or heparin did not undergo the acrosome reaction when exposed to calcium ionophore. In summary, alkaline pH has a profound detrimental effect on snow leopard sperm motility, and capacitation does not occur under conditions that normally promote this event in other felid species. These results clearly demonstrate a high degree of interspecific variation among felids in fundamental sperm function, and they provide evidence for the necessity of basic research when developing assisted reproduction in little-studied nondomestic species.
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Brown, J. L., Wasser, S. K., Wildt, D. E., & Graham, L. H. (1994). Steroid Metabolism and the Effectiveness of Fecal Assays for Assessing Reproductive Status in Felids. Biology of Reproduction, 50(suppl 1), 185.
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Berger, J., Buuveibaatar, B., Mishra, C. (). Globalization of the Cashmere Market and the Decline of Large Mammals in Central Asia. Conservation Biology, 27(4), 679–689.
Abstract: As drivers of terrestrial ecosystems, humans have replaced large carnivores in most areas, and
human influence not only exerts striking ecological pressures on biodiversity at local scales but also has
indirect effects in distant corners of the world. We suggest that the multibillion dollar cashmere industry
creates economic motivations that link western fashion preferences for cashmere to land use in Central
Asia. This penchant for stylish clothing, in turn, encourages herders to increase livestock production which
affects persistence of over 6 endangered large mammals in these remote, arid ecosystems. We hypothesized
that global trade in cashmere has strong negative effects on native large mammals of deserts and grassland
where cashmere-producing goats are raised. We used time series data, ecological snapshots of the biomass
of native and domestic ungulates, and ecologically and behaviorally based fieldwork to test our hypothesis.
In Mongolia increases in domestic goat production were associated with a 3-fold increase in local profits for
herders coexisting with endangered saiga (Saiga tatarica). That increasing domestic grazing pressure carries
fitness consequences was inferred on the basis of an approximately 4-fold difference in juvenile recruitment among blue sheep (Pseudois nayaur) in trans-Himalayan India. Across 7 study areas in Mongolia, India, and China’s Tibetan Plateau, native ungulate biomass is now <5% that of domestic species. Such trends suggest ecosystem degradation and decreased capacity for the persistence of native species, including at least 8 Asian endemic species: saiga, chiru (Pantholops hodgsoni), Bactrian camel (Camelus bactrianus), snow leopard (Panthera uncia), khulan (Equus hemionus), kiang (E. kiang), takhi (E. przewalski), and wild yak (Bos mutus). Our results suggest striking yet indirect and unintended actions that link trophic-level effects to markets induced by the trade for cashmere.
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Blomqvist, L., & Nystrom, V. (1980). On identifying snow leopards, Panthera uncia, by their facial markings. International Pedigree Book of Snow Leopards, , 159–167.
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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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