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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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Darehshuri, B. F. (1978). Threatened cats of Asia. Wildlife, 20(9), 396–400.
Abstract: Man's hand is turned against the wild cats wherever they occur, often due to the value of their fur, but also because of the danger they sometimes pose to domestic stock and even human beings. All the larger Asian cats are threatened, and on this and the following pages we look at three of them – the Asiatic cheetah, the Siberian tiger, and the snow leopard.
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Cornish, C. J., Selous, F.C., Ingersoll, E., Johnston, H., Maxwell, H., Hutchinson, H.N., Gregory, J.W., Lydekker, R. (1908). The Standard Library of Natural History: Vol. 1 Living animals of the world, mammals: Snow leopard or ounce. The Standard Library of Natural History, 1, 48.
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Clevenger, S. (1980). Snow leopards: Captivity perpetuates the species (Vol. XVI).
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Clevenger, S. A. (1980). Snow leopards born... and born... and born at OKC Zoo.
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Clevenger, S., S. (1979). Breeding snow leopards in the north 40.
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Clapp, M. Rare cat has back problems. San Antonio News.
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Chundawat, R. S. (1997). Elusive leopard of the mountains. In R. Manfredi (Ed.), In Danger: habitats, species and people (pp. 11–17). New Delhi, India: Ranthambhore Foundation.
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Chubykina, H. L., Shilo, R.A. (1981). A study of diurnal activity rhythms in snow leopards and lynx (Panthera uncia and Felix lynx) at Novosibirsk Zoo. International Zoo Yearbook, 21, 193–196.
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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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