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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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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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Wasser, S. (1998). Snow Leopard Genetics: New Techniques (Vol. xvi). 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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International Snow Leopard Trust. (1986). Indo-US Snow Leopard Project (Vol. No. 10). Seattle: Islt.
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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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Keen, B. (1984). The snow leopard (illicit furs). New Statesman, 107, 20.
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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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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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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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