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Subbotin, A. E., & Istomov, S. V. (2009). The population status of snow leopards Uncia uncia (Felidae, Carnivora) in the western Sayan Mountain Ridge. Doklady Biologicl Sciences, 425, 183–186.
Abstract: The snow leopard (Uncia uncial Schreber, 1776) is the most poorly studied species of the cat family in the world and, in particular, in Russia, where the northern periphery of the species area (no more than 3% of it) is located in the Altai-Hangai-Sayan range [1]. It is generally known that the existing data on the Russian part of the snow leopard population have never been a result of targeted studies; at best, they have been based on recording the traces of the snow leopard vital activity [2]. This is explained by the snow leopard's elusive behavior, inaccessibility of its habitats for humans, and its naturally small total numbers in the entire species area. All published data on the population status of the snow leopard in Russia, from the first descriptions of the species [3-6] to the latest studies [7, 8] are subjective, often speculative, and are not confirmed by
quantitative estimates. It is obvious, however, that every accurate observation of this animal is of particular interest [9]. The purpose of our study was to determine the structure and size of the population group presumably inhabiting the Western Sayan mountain ridge at the northern boundary of the species area
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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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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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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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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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White, S. D., Stannard, A. A., Ihrke, P. J., & Rosser, E. J. (1981). Therapy of demodicosis in snow leopard challenged. J Am Vet Med Assoc, 178(9), 877–878.
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Hast, M. H. (1989). The larynx of roaring and non-roaring cats. J Anat, 163, 117–121.
Abstract: Dissections were made of the larynges of 14 species of the cat family, with representative specimens from all genera. It was found that the vocal folds of the larynx of genus Panthera (with the exception of the snow leopard) form the basic structure of a sound generator well- designed to produce a high acoustical energy. Combined with an efficient sound radiator (vocal tract) that can be adjusted in length, a Panthera can use its vocal instrument literally to blow its own horn with a 'roar'. Also, it is proposed that laryngeal morphology can be used as an anatomical character in mammalian taxonomy.
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Chaudhuri, S., Mukherjee, S. K., Chatterjee, A., & Ganguli, J. L. (1992). Isolation of P multocida F-3, 4 from a stillborn snow leopard. Vet Rec, 130(2), 36.
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Slifka, K., Stacewicz-Sapuntzakis, S. M., Bowen, P., & Crissey, S. (1999). A Survey of Serum and Dietary Carotenoids in Captive Wild Animals. The Journal of Nutrition, 129, 380–390.
Abstract: Accumulation of carotenoids varies greatly among animal species and is not fully characterized.
Circulating carotenoid concentration data in captive wild animals are limited and may be useful for their management.
Serum carotenoid concentrations and dietary intakes were surveyed and the extent of accumulation
categorized for 76 species of captive wild animals at Brookfield Zoo. Blood samples were obtained opportunistically
from 275 individual animals immobilized for a variety of reasons; serum was analyzed for a- and b-carotene,
lutein 1 zeaxanthin, lycopene, b-cryptoxanthin and canthaxanthin. Total carotenoid content of diets was calculated
from tables and chemical analyses of commonly consumed dietary components. Diets were categorized as
low, moderate or high in carotenoid content as were total serum carotenoid concentrations. Animals were
classified as unknown, high, moderate or low (non-) accumulators of dietary cartenoids. Nonaccumulators had total
serum carotenoid concentrations of 0-101 nmol/L, whereas accumulators had concentrations that ranged widely,
from 225 to 35,351 nmol/L. Primates were uniquely distinguished by the widest range of type and concentration
of carotenoids in their sera. Most were classified as high to moderate accumulators. Felids had high accumulation
of b-carotene regardless of dietary intake, whereas a wide range of exotic birds accumulated only the xanthophylls,
lutein 1 zeaxanthin, canthaxanthin or cryptoxanthin. The exotic ungulates, with the exception of the bovids, had
negligible or nondetectable carotenoid serum concentrations despite moderate intakes. Bovids accumulated only
b-carotene despite moderately high lutein 1 zeaxanthin intakes. Wild captive species demonstrated a wide variety
of carotenoid accumulation patterns, which could be exploited to answer remaining questions concerning carotenoid
metabolism and function.
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