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Allen, P. (2002). Conservation Increases Crafts Income (Vol. Winter, 2002).
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Woodroffe, R., & Ginsberg, J. R. (1998). Edge effects and the extinction of populations inside protected areas. Science Washington D.C., 280(5372), 2126–2128.
Abstract: Theory predicts that small populations may be driven to extinction by random fluctuations in demography and loss of genetic diversity through drift. However, population size is a poor predictor of extinction in large carnivores inhabiting protected areas. Conflict with people on reserve borders is the major cause of mortality in such populations, so that border areas represent population sinks. The species most likely to disappear from small reserves are those that range widely-and are therefore most exposed to threats on reserve borders-irrespective of population size. Conservation efforts that combat only stochastic processes are therefore unlikely to avert extinction.
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Blomqvist, L. (1989). Captive Snow Leopard Report for 1989. International Zoo News, 265, 5–14.
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Oli, M. K., Taylor, I. R., & Rogers, M. K. (1993). Diet of the snow leopard (Panthera uncia) in the Annapurna Conservation Area, Nepal. Journal of Zoology London, 231(3), 365–370.
Abstract: The diet of the snow leopard (Panthera uncia) was studied from 213 scats collected between April 1990 and February 1991 in the Annapurna Conservation Area, Nepal. Seven species of wild and five species of domestic mammals were taken, as well as an unidentified mammal and birds. Blue sheep (Pseudois nayaur) were the most frequently eaten prey. Himalayan marmots (Marmota himalayana) were also important, except in winter when they were hibernating. During winter, snow leopards ate more Royle's pika (Ochotona roylei) and domestic livestock. Yaks were eaten more frequently than other livestock types.
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Oli, M. K. (1993). A key for the identification of the hair of mammals of a snow leopard (Panthera uncia) habitat in Nepal. Journal of Zoology London, 231(1), 71–93.
Abstract: Analysis of prey remains in scats, particularly hairs, in widely used to study diet of mammalian predators, but identification of hair is often difficult because hair structures vary considerably both within and between species. Use of photographic reference of diagnostically important hair structures from mammals occurring in a predator's habitat has been found to be convenient for routine identification. A photographic reference key was developed for the identification of hairs of the mammals known to occur in a snow leopard (Panthera uncia) habitat in the Annapurna Conservation Area, Nepal. The key included a photographic reference of the diagnostic hair structures of nine species of wild and five species of domestic mammals. The cross-sectional appearance, shape and arrangement of medulla, the ratio of cortex to medulla, and the form and distribution of pigment in medulla and cortex were important diagnostic aids in the identification of hairs.
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Karesh, W. B., & Kunz, L. L. (1986). Bilateral testicular seminoma in a snow leopard. J Am Vet Med Assoc, 189(9), 1201.
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Mainka, S. A. (1986). Bilateral separation of the olecranon and proximal epiphysis from the ulnar diaphysis in a snow leopard cub. J Am Vet Med Assoc, 189(9), 1204–1205.
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Paul, H. A., Bargar, W. L., & Leininger, R. (1985). Total hip replacement in a snow leopard. J Am Vet Med Assoc, 187(11), 1262–1263.
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Macdonald, A. A., & Johnstone, M. (1995). Comparative anatomy of the cardiac foramen ovale in cats (Felidae), dogs (Canidae), bears (Ursidae) and hyaenas (Hyaenidae). J Anat, 186 ( Pt 2), 235–243.
Abstract: The structure of the foramen ovale from 16 species representing 4 carnivore families, the Felidae, Canidae, Ursidae and Hyaenidae, was studied using the scanning electron microscope. The Felidae were represented by 9 domestic cat fetuses (Felis catus), 2 snow leopard neonates (Uncia uncia), an ocelot neonate (Leopardus pardalis), 2 lion neonates (Panthera leo), a panther neonate (Panthera pardus) and 3 tigers (Neofelis tigris), comprising 2 fetuses and a neonate. The Canidae were represented by a golden jackal neonate (Canis aureus), a newborn wolf (Canis lupus), 8 domestic dog fetuses (Canis familiaris), 3 red fox neonates (Vulpes vulpes) and a dhole neonate (Cuon alpinus). The Ursidae were represented by a brown bear neonate (Ursus arctos), a day-old grizzly bear cub (Ursus arctos horribilis), a polar bear neonate (Ursus maritimus), and 2 additional bear fetuses (species unknown). The Hyaenidae were represented by a striped hyaena neonate (Hyaena hyaena). In each species, the foramen ovale, when viewed from the terminal part of the caudal vena cava, had the appearance of a short tunnel. A thin fold of tissue, the developed remains of the embryonic septum primum, extended from the distal end of the caudal vena cava for a variable distance into the lumen of the left atrium and contributed towards the 'tunnel' appearance in all specimens. It constituted a large proportion of the tube, and its distal end was straight-edged. There was fibrous material underlying the endothelium of the flap, the apparent morphology of which suggested that it comprised cardiac muscle.(ABSTRACT TRUNCATED AT 250 WORDS)
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Schaller, G. (1993). Tibet's remote Chang Tang: in a high and sacred realm. National Geog., 184(2), 62–87.
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