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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Keen, B. (1984). The snow leopard (illicit furs). New Statesman, 107, 20.
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Heinen, J. T., & Leisure, B. (1993). A new look at Himalayan Fur Trade. Oryx, 27(4), 231–238.
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International Snow Leopard Trust. (1986). Indo-US Snow Leopard Project (Vol. No. 10). Seattle: Islt.
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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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Wasser, S. (1998). Snow Leopard Genetics: New Techniques (Vol. xvi). Seattle: Islt.
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Roth, T. L., Swanson, W. F., & Wildt, D. E. (1995). Snow leopard (Panthera unica) sperm longevity in vitro is not influenced by protein or energy source supplements but is affected by buffer source. Theriogenology, 43(1), 309.
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Hunter, D. O. (1991). Science and Spirit:GIS tracks the elusive snow leopard. GeoInfo Systems, Jan, 21–28.
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Bold, A., & Dorzhzunduy, S. (1976). Report on Snow Leopards in the Southern Spurs of the Gobi Altai. (Vol. 11, pp. 27–43).
Abstract: Estimates a population of 170-230 snow leopard within an area of 6600 km2 in Southern Gobi
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Zhirnov, L., & Ilyinsky, V. (1986). The Great Gobi National Park – a refuge for rare animals of the Central Asian deserts. Moscow: Centre for International Projects, GKNT.
Abstract: Discusses snow leopard distribution in Great Gobi National Park
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