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Kuznetsnov, G. U., & Matyushkin, E. N. (1980). The snow leopard hunts. Int.Ped.Book of Snow Leopards, 11, 44–48.
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Sitwell, N. (1972). The Snow Leopard in Pakistan. Animals, 14(6), 256–259.
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Turner, L. (1980). Oklahoma City Zoo-Twenty Nine Snow Leopards. Int.Ped Book of Snow Leopards, 2, 96–111.
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Rieger, I. (1980). Some difficulty breeding ounces, (Uncia uncia) at zoological gardens. Int.Ped Book of Snow Leopards, 2, 76–95.
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Liao, Y. F. (1985). The Geographical Distribution of Ounces in Qinghai Province. Acta Theriologica Sinica, 5(3), 183–188.
Abstract: This paper deals with the geographical distribution of ounces (Panthera uncia) in Qinghai Province. Ounces are distributed in 20 counties- Guide, Huzhu, Menyuan, Qilian, Tianjun, Dulan, Golmud, Guinan, Xinghai, Zhidoi, Zadoi, Nangqen, Yushu, Chindu, Qumarleb, Madio, Maqen, Jigzhi, Baima, Darlag. Among them, there fore 4 counties- Qilian, Tianjun, Dulan, Zadoi, in which the number of ounces are bigger. The number of ounces are shown in table 2. There are altogether 73 ounces (40 male, 33 female) which is supported to every park of China for ornamental, they were captured by fellow-villagers, and 44 ounces (23 male, 21 female) of them are below 6 months old, 9 ounces (6 male, 3 female) of them are 1 year old, 2 ounces (male) are 2 years old, and 18 ounces (9 male, 9 female) are adults.
Ounces live at an altitude of 3000-4100 metres above the sea, and prefer to eat Bharal (Pseudois noyour). Its breeding period goes from April to June, the number of embryos being 2-3.
A female ounce was successfully reproduced for the first time at Xining People's Park of China, in Spetember, 1984, and she gave birth to 3 young ounces.
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Yanfa, L., & Huanwen, L. (1986). A preliminary study on the rearing and breeding of ounce. Acta Theriologica Sinica, 6(2), 93–99.
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Yu, N. Z. C., Wang, X., He, G., Zhang, Z., Zhang, A., Lu, W., et al. (1996). A revision of genus Uncia Gray, 1854 based on mitochondrial DNA restriction site maps. Acta Theriologica Sinica, 16(2), 105–108.
Abstract: The Snow leopard (Panthera uncia) is one of the most threatened wild big cats within its range of distribution, however, the question of its systematic status is a matter of debate. Is it a member of genus Panthera, or is it in its own genus (Uncia)? The analysis of genetic difference at the DNA level may provide useful data to clarify the issue. In the present study, ten hexanucleotide-specific restriction endonucleases were used to evaluate the patterns of mitochondrial DNA variation between the Snow leopard and leopard (P. pardus). The molecular size of mtDNA from the two species was about 16.5 kb. Ten enzymes surveyed 32-34 restriction sites, which corresponded to 192 apprx 204 base pairs, or 1.16% apprx 1.24% of the total mtDNA molecule. A total of 45 restriction sites were mapped; of these sites, twenty-four, which correspond to 53.3% of the total sites, were variable. The sequence divergence between them was 0.075 33, which was undoubtedly in the species-level distinction but did not reach the genus level. Therefore, the Snow leopard should be placed in the genus Panthera rather than in its own ganus. It also seems reasonable to recognize Uncia as a valid subgenus. This conclusion not only support but also supplement the viewpoint of Simpson who treated Uncia as a subgenus within Panthera.
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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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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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Munson, L., & Worley, M. B. (1991). Veno-occlusive disease in snow leopards (Panthera uncia) from zoological parks. Vet Pathol, 28(1), 37–45.
Abstract: Livers from 54 snow leopards, 4 days to 23 years old, that had died in 23 US zoos, were evaluated histopathologically to determine if the hepatic fibrosis, which has been noted to be prevalent in this species, was due to chronic active hepatitis from hepadnaviral infection, Ito cell proliferation, or hemosiderosis. Forty-two of 54 snow leopards had subintimal vascular fibrosis with partial or total occlusion of central and sublobular veins (veno-occlusive disease) of unknown origin. All 21 leopards older than 5 years were affected. Four leopards had chronic active hepatitis, and 12 leopards had cholangiohepatitis; but these lesions were not connected anatomically to central and sublobular venous fibrosis. Hepatocellular and Kupffer cell siderosis and Ito cell proliferation were prevalent and often coexisted with perisinusoidal, central, and sublobular venous fibrosis; but fibrosis was present in leopards without siderosis or Ito cell proliferation. The pattern and prevalence of veno-occlusive disease in these leopards was similar to that reported in captive cheetah (Acinonyx jubatus), suggesting that a common extrinsic factor may cause the majority of hepatic disease in these large felid animals in captivity.
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