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Spitsin, V., & Koshkarev, E. (1988). Status and Distribution of Snow Leopard in Kirgizia (U.S.S.R.). In H.Freeman (Ed.), (pp. 21–23). International Snow Leopard Trust and Wildlife Institute of India.
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Stockley, G. (1936). Stalking in the Himalayas and Northern India. London: Herbert Jenkins.
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Stockley, G. (1928). Big Game Shooting In the Indian Empire. London: Constable.
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Sukhbat, K., & Munkhtsog, B. (1997). Density and Distribution of Ibex and Argali Sheep in Mongolia. In R.Jackson, & A.Ahmad (Eds.), (pp. 121–123). Lahore, Pakistan: Islt.
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Sundberg, J. P., Van Ranst, M., Montali, R., Homer, B. L., Miller, W. H., Rowland, P. H., et al. (2000). Feline papillomas and papillomaviruses. Vet Pathol, 37(1), 1–10.
Abstract: Papillomaviruses (PVs) are highly species- and site-specific pathogens of stratified squamous epithelium. Although PV infections in the various Felidae are rarely reported, we identified productive infections in six cat species. PV-induced proliferative skin or mucous membrane lesions were confirmed by immunohistochemical screening for papillomavirus-specific capsid antigens. Seven monoclonal antibodies, each of which reacts with an immunodominant antigenic determinant of the bovine papillomavirus L1 gene product, revealed that feline PV capsid epitopes were conserved to various degrees. This battery of monoclonal antibodies established differential expression patterns among cutaneous and oral PVs of snow leopards and domestic cats, suggesting that they represent distinct viruses. Clinically, the lesions in all species and anatomic sites were locally extensive and frequently multiple. Histologically, the areas of epidermal hyperplasia were flat with a similarity to benign tumors induced by cutaneotropic, carcinogenic PVs in immunosuppressed human patients. Limited restriction endonuclease analyses of viral genomic DNA confirmed the variability among three viral genomes recovered from available frozen tissue. Because most previous PV isolates have been species specific, these studies suggest that at least eight different cat papillomaviruses infect the oral cavity (tentative designations: Asian lion, Panthera leo, P1PV; snow leopard, Panthera uncia, PuPV-1; bobcat, Felis rufus, FrPV; Florida panther, Felis concolor, FcPV; clouded leopard, Neofelis nebulosa, NnPV; and domestic cat, Felis domesticus, FdPV-2) or skin (domestic cat, F. domesticus, FdPV-1; and snow leopard, P. uncia, PuPV-2).
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Sunquist, F. (1997). Where cats and herders mix. (snow leopards in Tibet and Mongolia). International Wildlife, 27(1), 27–33.
Abstract: The snow leopard inhabits a huge range of territory which encompasses some of Central Asia's most bleak and inhospitable terrains. The animal herders in these regions are desperately poor and yet they have agreed to cooperate with conservation groups in protecting the snow leopard. The World Wildlife Foundation has worked to create a refuge on the Pakistan-China border. Sheep herders near Askole, a village in the Baltistan region of northern Paksitan, drive their flocks past stone enclosures. The area is also home to snow leopards. With their natural prey dminished, leopards in 13 countries of central Asia occasionally feed on livestock, putting the cats on a collision course with mountain peoples.
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Suryawanshi, K. R. (2009). Towards snow leopard prey recovery: understanding the resource use strategies and demographic responses of bharal Pseudois nayaur to livestock grazing and removal; Final project report.
Abstract: Decline of wild prey populations in the Himalayan region, largely due to competition with livestock, has been identified as one of the main threats to the snow leopard Uncia uncia. Studies show that bharal Pseudois nayaur diet is dominated by graminoids during summer, but the proportion of graminoids declines in winter. We explore the causes for the decline of graminoids from bharal winter diet and resulting implications for bharal conservation. We test the predictions generated by two alternative hypotheses, (H1) low graminoid availability caused by livestock grazing during winter causes bharal to include browse in their diet, and, (H2) bharal include browse, with relatively higher nutrition, to compensate for the poor quality of graminoids during winter. Graminoid availability was highest in areas without livestock grazing, followed by areas with moderate and intense livestock grazing. Graminoid quality in winter was relatively lower than that of browse, but the difference was not statistically significant. Bharal diet was dominated by graminoids in areas with highest graminoid availability. Graminoid contribution to bharal diet declined monotonically with a decline in graminoid availability. Bharal young to female ratio was three times higher in areas with high graminoid availability than areas with low graminoid availability. No starvation-related adult mortalities were observed in any of the areas. Composition of bharal winter diet was governed predominantly by the availability of graminoids in the rangelands. Since livestock grazing reduces graminoid availability, creation of livestock free areas is necessary for conservation of grazing species such as the bharal and its predators such as the endangered snow leopard in the Trans-Himalaya.
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Suryawanshi, K. R., Bhatnagar, Y., & Mishra, C. (2009). Why should a grazer browse? Livestock impact on winter resource use by bharal Pseudois nayaur
. Oecologia, , 1–10.
Abstract: Many mammalian herbivores show a temporal diet variation between graminoid-dominated and browse dominated diets. We determined the causes of such a diet shift and its implications for conservation of a medium sized ungulate-the bharal Pseudois nayaur. Past studies show that the bharal diet is dominated by graminoids (>80%) during summer, but the contribution of graminoids declines to about 50% in winter. We tested the predictions generated by two alternative hypotheses explaining the decline: low graminoid availability during winter causes bharal to include browse in their diet; bharal include browse, with relatively higher nutritional quality, in their diet to compensate for the poor quality of graminoids during winter. We measured winter graminoid availability in areas with no livestock grazing, areas with relatively moderate livestock grazing, and those with intense livestock grazing pressures. The chemical composition of plants contributing to the bharal diet was analysed. The bharal diet was quantiWed through signs of feeding on vegetation at feeding locations. Population structures of bharal populations were recorded using a total count method. Graminoid availability was highest in areas without livestock grazing, followed by areas with moderate and intense livestock grazing. The bharal diet was dominated by graminoids (73%) in areas with highest graminoid availability. Graminoid contribution to the bharal diet declined monotonically (50, 36%) with a decline in graminoid availability. Bharal young to female ratio was 3 times higher in areas with high graminoid availability than areas with low graminoid availability. The composition of the bharal winter diet was governed predominantly by the availability of graminoids in the rangelands. Our results suggest that bharal include more browse in their diet during winter due to competition from livestock for graminoids. Since livestock grazing reduces graminoid availability, creation of livestock-free areas is necessary for the conservation of grazing species such as the bharal and its predators including the endangered snow leopard in the Trans-Himalaya.
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Taber, R. (1988). Long Term Research in Snow Leopard Conservation. In H.Freeman (Ed.), (pp. 255–259). India: International Snow Leopard Trust and Wildlife Institute of India.
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Taber, R. D. (1988). Toward a Free-Living Snow Leopard Recovery Plan. In H.Freeman (Ed.), (261). Usa: ISLT and Wildlife Institute of India.
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Taryannikov, V. I. (1986). Distribution, biology and current state of the number of the rare predatory mammals in W. Gissar. The Ecology, Protection, and Acclimatization of Vertebrates in Uzbekistan. Tashkent.
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Thorel, M. F., Karoui, C., Varnerot, A., Fleury, C., & Vincent, V. (1998). Isolation of Mycobacterium bovis from baboons, leopards and a sea-lion. Vet Res, 29(2), 207–212.
Abstract: This study reports on two series of cases of Mycobacterium bovis infection in zoo animals. The first was in a captive population of baboons (Papio hamadryas) and the second in a mixed group of wild mammals, including four leopards (Panthera uncia and Panthera pardus) and a sea-lion (Otaria byrona). The isolation and identification of strains of M. bovis confirmed the presence of M. bovis infections in both zoos. The epidemiological study using genetic markers such as the IS6110-based DNA fingerprinting system made it possible to differentiate between M. bovis strains. The M. bovis strains isolated from baboons were shown to contain a single IS6110 copy, as usually do cattle isolates, whereas the M. bovis strains isolated from the other exotic animals presented multiple copies. This finding suggests that the origin of the contamination for the baboons in zoo A could be related to cattle. The origin of the contamination for the leopards and sea-lion in zoo B is more difficult to determine. In conclusion, the authors suggest some recommendations for avoiding outbreaks of tuberculosis infections in zoos.
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Trepanier, L. A., Cribb, A. E., Spielberg, S. P., & Ray, K. (1998). Deficiency of cytosolic arylamine N-acetylation in the domestic cat and wild felids caused by the presence of a single NAT1-like gene. Pharmacogenetics, 8(2), 169–179.
Abstract: The purpose of this study was to determine the molecular basis for a relative deficiency in the cat of cytosolic arylamine N- acetyltransferase (NAT), an enzyme family that is important in the metabolism of xenobiotics and that normally consists of at least two related enzymes, NAT1 and NAT2. N-acetyltransferase in feline liver showed high affinity (mean Km = 2.1 microM) for p-aminobenzoic acid, an NAT1 selective substrate in humans and rabbits, but showed a very poor affinity (mean Km > 10 mM) for sulfamethazine, an NAT2 selective substrate in humans and rabbits. Immunoreactive N-acetyltransferase was detected in feline liver, bladder and colon using an NAT1-specific antipeptide antibody, but was not detected in any tissues using an NAT2- specific antibody. Southern blot analysis of genomic DNA demonstrated a single band in domestic cats using each of six restriction digests; single bands were also found on Southern blot analysis of six wild felids. The deduced amino acid sequence of the central portion of feline N-acetyltransferase, obtained by polymerase chain reaction amplification in both domestic cats and seven wild felids (lion, tiger, lynx, snow leopard, bobcat, Asian leopard cat and cheetah), contained three residues, Phe125, Arg127, and Tyr129, which determine NAT1-like substrate specificity in humans. These results support the conclusion that cytosolic arylamine N-acetylation activity is low in the cat because of the presence of a single N-acetyltransferase that has substrate specificity, immunogenicity and sequence characteristics similar to human NAT1, and that the unusual presence of only a single N- acetyltransferase gene appears to be a family wide trait shared by other felids.
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Tserendeleg, J. (1997). Status and Conservation of Snow Leopard in Mongolia. In R.Jackson, & A.Ahmad (Eds.), (pp. 42–47). Lahore, Pakistan: International Snow Leopard Trust.
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Tserendeleg, J. (1994). On Protection and Survey of Snow Leopards in Mongolia. In J.L.Fox, & D.Jizeng (Eds.), (pp. 43–46). Usa: Islt.
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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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Villarrubia, C., & Jackson, R. (1994). Snow Leopard Conservation on a Regional Basis: Elements in Planning Protected Areas. In J.L.Fox, & D.Jizeng (Eds.), (pp. 253–263). Usa: Islt.
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Volozheninov, N. N. (1985). Rare and vanishing mammals and birds in S Uzbekistan. Ecology and protection of the rare and vanishing vertebrates in Uzbekistan, Tashkent.
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Wack, R. F., & Kramer, L. W. (1995). Multifocal osteomyelitis in a young snow leopard (Panthera uncia). Journal of Zoo and Wildlife Medicine, 26(4), 553–563.
Abstract: A 5-mo-old male snow leopard (Panthera uncia) was presented for mild rear leg lameness. Osteomyelitis was suspected on the basis of radiographic changes and confirmed by histopathology of a biopsy sample from the affected bone. Aerobic cultures of the biopsies repeatedly grew Klebsiella oxytoca. Repeated anaerobic and fungal cultures did not result in growth. The leopard was treated unsuccessfully with cefadroxil, chloramphenicol, and trimethoprim/sulfadiazine despite apparent in vitro sensitivity to these antibiotics. Successful resolution was eventually achieved with enrofloxacin, 7.5 mg/kg p.o. b.i.d. for 60 days. The number of bones involved (right humerus, right and left ulna, right and left radius, right and left femur, right and left tibia, mandible, right metatarsus) made this an unusual presentation of osteomyelitis.
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Wajrak, A. (1994). Snow Leopard Skins in Poland (Polowanie Na Sniezna Pantere).
Abstract: Full Text: In 1991, Dr Andrzej Kruszewicz of the Institute of Ecology of the Polish Academy of Sciences saw a “quite fresh” snow leopard skin on sale by a Russian in a Warsaw market for three million Polish zlotys ($300). A few weeks later he saw another skin in a shop in the centre of Warsaw. In spring 1992, Marcin Waslawski from the Institute of Geography saw a snow leopard skin in the same market for the equivalent of $200. The seller was an Asian from a former Soviet Republic. In summer 1992, Wajrak himself saw a snow leopard skin in a hunters' shop in Warsaw and in winter saw one in the home of a Polish hunter, who said it was a gift from a Mongolian friend. In winter 1994, a student from Britain saw a Polish long coat of snow leopard skins in Bialowieza. Wajrak saw a skin in a Warsaw shop, which the owner said was 15-20 years old; he got it from a Polish diplomat who had been in Mongolia and had three snow leopard skins. The skin was priced at the equivalent of $1,000. Wajrak added that he had been told that it was possible to buy tiger skins from Russians in Poland and he was trying to find one; I have not heard from him since.
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Wang, X., & Schaller, G. B. (1996). Status of large mammals in Western Inner Mongolia, China. Journal of East China Normal University (Special Issue of Zoology), , 93–104.
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Wangchuk, T. R. (1992). Snow Leopard: Its Management with Emphasis on Bhutan.
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Ward, A. E. (1921). Game animals of Kashmir and adjacent hill provinces. J.of Bombay Natural Historical Society., 29, 23–35.
Abstract: comments that snow leopard may take blue sheep as prey
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Wasser, S. (1998). Snow Leopard Genetics: New Techniques (Vol. xvi). Seattle: Islt.
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Watanabe, M., Sugano, S., Togashi, T., Imai, J., Uchida, K., Yamaguchi, R., et al. (2000). Molecular cloning and phylogenetic analysis of canine beta-casein. DNA Seq, 11(3-4), 295–300.
Abstract: A canine beta-casein cDNA was isolated from mammary tissue by polymerase chain reaction (PCR) using degenerate primers. It encodes 250 amino acids protein containing the conserved sequence motif of beta- casein. It showed the highest homology with snow-leopard (Uncia uncia (55-62% identity). It also showed 44-53% identity with human, 33-42%, identity with mouse, 29-37%, identity with rat, 43-53% identity with rabbit, 41-48% identity with pig, 44-51% identity with cattle and 44- 50% identity with sheep. A 1.2-kb mRNA was detected in mammary tissue by Northern blot analysis. Phylogenetic analysis revealed that canine beta-casein formed a branch with lesser panda and snow leopard, which were grouped into carnivore.
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