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Schaller, G. B., Jurang, R., & Mingjiang, Q. (1988). Status of snow leopard (Panthera-uncia) in Qinghai-Province and Gansu Province-China. Biological Conservation, 45(3), 179–194.
Abstract: The status and distribution of the snow leopard Panthera uncia was investigated in two provinces of China. The cats occur over about 65,000km2 or 9% of the Qinghai Province, and in a few places along the western edge of Gansu Province. In many areas the animals have in recent decades been decimated or locally eradicated, as have their prey. Counts of wild ungulates in 9 mountain block, totalling 1375km2, known for abundant wildlife, had an average of 1.4-5.4 animals km2, principally blue sheep Psuedois nayaur, which together with marmot Marmota himalayana, represent the snow leopards main prey. Possibly 650 snow leopards survive in Qinghai but shooting and trapping of this legally protected animal and the hunting of blue sheep for local consumtion and export threaten their existence.
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Seidensticker, J., & Lumpkin, S. (1996). The adaptable leopard; unfortunately it's no match for modern man. Wildlife Conservation, 99(3), 52.
Abstract: Abstract: Leopards' adaptability has become the species' vulnerability. The animals do not hesitate to eat rotting flesh and will come back repeatedly to their meal, if disturbed. People have taken advantage of this by lacing carcasses with poison. Leopards are moderate in size compared to other cats, are stealthy and can live in areas as diverse as rain forests and deserts.
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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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Clyde, V. L., Ramsay, E. C., & Bemis, D. A. (1997). Fecal shedding of Salmonella in exotic felids. J.Zoo Wildl.Med, 28(2), 148–152.
Abstract: The authors discuss the occurrence of salmonellosis in collections of exotic felids. Data suggest that zoo employees having contact with cat feces or raw diets have a high rate of occupational exposure to Salmonella and should exercise appropriate hygienic precautions. pcp
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Dzhanyspaev, A. D. (1991). Hunting Behavior of the Snow Leopard at the Alma-Atinski Nature Reserve (Vol. ix). Seattle: International Snow Leopard Trust.
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Guerrero, D. (1998). Animal behavior concerns & solutions: snow leopard (Uncia uncia) evaluation, zoo. Anim.Keepers' Forum, 25(2), 56–58.
Abstract: The author offers advice on how a captive-raised snow leopard cub could be acclimated to humans so it could be used as a zoo “ambassador”. The cub had negative experiences with humans and lacked socialization with other animals and conspecifics. Methods of avoiding and redirecting the cub's aggressive behavior are suggested. lgh.
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Jackson, R., & Ahlborn, G. (1989). Snow leopards (Panthera- uncia) in Nepal – home range and movements. National Geographic Research, 5(2), 161–175.
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Jalanka, H. H. (1989). Medetomidine-induced and ketamine-induced immobilization of snow leopards (Panthera uncia) doses, evaluation and reversal by atipamezole. Journal of Zoo and Wildlife Medicine, 20(2), 154–162.
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Jalanka, H. H. (1989). Evaluation and comparison of 2 ketamine-based immobilization techniques in snow leopards (Panthera uncia). Journal of Zoo and Wildlife Medicine, 20(2), 163–169.
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Johnson, W. E., Dratch, P. A., Martenson, J. S., & O'Brien, S. J. (1996). Resolution of recent radiations within three evolutionary lineages of Felidae using mitochondrial restriction fragment length polymorphism variation. Journal of Mammalian Evolution, 3(2), 97–120.
Abstract: Patterns of mitochondrial restriction fragment length polymorphism (RFLP) variation were used to resolve more recent relationships among the species of the Felidae ocelot lineage, domestic cat lineage, and pantherine lineage. Twenty-five of 28 restriction enzymes revealed site variation in at least 1 of 21 cat species. The ocelot lineage was resolved into three separate sister taxa groups: Geoffroy's cat (Oncifelis geoffroyi) and kodkod (O. guigna), ocelot (Leopardus pardalis) and margay (L. wiedii), and pampas cat (Lynchailurus colocolo) and most of the tigrina samples (Leopardus tigrina). Within the domestic cat lineage, domestic cat (Felis catus), European wild cat (F. silvestris), and African wild cat (F. libyca) formed a monophyletic trichotomy, which was joined with sand cat (F. margarita) to a common ancestor. Jungle cat (F. chaus) and black-footed cat (F. nigripes) mtDNAs diverged earlier than those of the other domestic cat lineage species and are less closely related. Within the pantherine lineage, phylogenetic analysis identified two distinct groups, uniting lion (P. leo) with leopard (P. pardus) and tiger (P. tigris) with snow leopard (P. uncia).
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Kinsel, M. J., Kovarik, P., & Murnane, R. D. (1998). Gastric spiral bacteria in small felids. Journal-of-Zoo-and-Wildlife-Medicine, 29(2), 214–220.
Abstract: Nine small cats, including one bobcat (Felis rufus), one Pallas cat (F. manul), one Canada lynx (F. lynx canadensis), two fishing cats (F. viverrina), two margays (F. wiedii), and two sand cats (F. margarita), necropsied between June 1995 and March 1997 had large numbers of gastric spiral bacteria, whereas five large cats, including one African lion (Panthera leo), two snow leopards (P. uncia), one Siberian tiger (P. tigris altaica), and one jaguar (P. onca), necropsied during the same period had none. All of the spiral organisms from the nine small cats were histologically and ultrastructurally similar. Histologically, the spiral bacteria were 5-14 mum long with five to nine coils per organism and were located both extracellularly within gastric glands and surface mucus, and intracellularly in parietal cells. Spiral bacteria in gastric mucosal scrapings from the Canada lynx, one fishing cat, and the two sand cats were gram negative and had corkscrew-like to tumbling motility when viewed with phase contrast microscopy. The bacteria were 0.5-0.7 mum wide, with a periodicity of 0.65-1.1 mum in all cats. Bipolar sheathed flagella were occasionally observed, and no periplasmic fibrils were seen. The bacteria were extracellular in parietal cell canaliculi and intracellular within parietal cells. Culture of mucosal scrapings from the Canada lynx and sand cats was unsuccessful. Based on morphology, motility, and cellular tropism, the bacteria were probably Helicobacter-like organisms. Although the two margays had moderate lymphoplasmacytic gastritis, the other cats lacked or had only mild gastric lymphoid infiltrates, suggesting that these organisms are either commensals or opportunistic pathogens.
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Koshkarev, E. (1994). Poaching in Former USSR (Vol. xii). Seattle: International Snow Leopard Trust.
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Koshkarev, E. P. (1992). Range Structure, Numbers and Population Status of the Snow Leopard in the Tien Shan (Vol. x). Seattle: International Snow Leopard Trust.
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McVittie, R. (1978). Nursing behavior of snow leopard cubs. Applied-Animal-Ethology, 4(2), 159–168.
Abstract: Reports that a preliminary project on nursing behavior in 3 young snow leopards revealed 2 phases in suckling pattern: nonnutritive and nutritive. The latter was distinguished by stereotypic rhythmical movements of the ears associated with swallowing. The cubs also demonstrated a teat preference, but the adaptive significance of such preferences and the accompanying agonistic behavior were unclear. (27 ref) (PsycINFO Database Record (c) 2000 APA, all rights reserved)(unassigned)
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Nolte-Wilson, B. (1990). Soveriegn of menaced realm: the snow leopard. Natura WWF-Pakistan Newsletter, 9(2), 3–9.
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Oli, M. K. (1996). Seasonal patterns in habitat use of blue sheep Pseudois nayaur (Artiodactyla, Bovidae) in Nepal. Mammalia, 60(2), 187–193.
Abstract: Blue sheep (Pseudois nayaur) are the main prey of the endangered snow leopard (Panthera uncia) as well as an important game species in Nepal. A knowledge of how blue sheep utilize their habitat is essential for the scientific management of the sheep and for the conservation of the snow leopard, but we only have a limited understanding of this aspect of blue sheep ecology. I studied the habitat use pattern of blue sheep by direct observation in the Anna-purna Conservation Area, Nepal where they occur sympatrically with the snow leopard. The sheep used grassland habitats more frequently during pre-parturition (spring) and post-parturition (autumn) than other habitat types, but scrub and grassland habitats were used equally frequently during the rut (winter). The sheep used smooth undulating slopes of medium steepness (<40 degrees) on southerly aspects within the elevation range of 4,200-4,600 m most frequently in all seasons, and there was no evidence of seasonal migration along the elevation gradient. When not in broken landforms (e.g., cliff, landslides), the sheep maintained proximity (less than or equal to 150 m) to such features suggesting their importance as escape cover (i.e., from predators). The use of habitat components by blue sheep appeared to be related to the distribution of foraging areas and escape cover.
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Pollock, R. V., & Carmichael, L. E. (1983). Use of modified live feline panleukopenia virus vaccine to immunize dogs against canine parvovirus. Am J Vet Res, 44(2), 169–175.
Abstract: Modified live feline panleukopenia virus (FPLV) vaccine protected dogs against canine parvovirus (CPV) infection. However, unlike the long- lived (greater than or equal to 20-month) immunity engendered by CPV infection, the response of dogs to living FPLV was variable. Doses of FPLV (snow leopard strain) in excess of 10(5.7) TCID50 were necessary for uniform immunization; smaller inocula resulted in decreased success rates. The duration of immunity, as measured by the persistence of hemagglutination-inhibiting antibody, was related to the magnitude of the initial response to vaccination; dogs with vigorous initial responses resisted oronasal CPV challenge exposure 6 months after vaccination, and hemagglutination-inhibiting antibodies persisted in such dogs for greater than 1 year. Limited replication of FPLV in dogs was demonstrated, but unlike CPV, the feline virus did not spread to contact dogs or cats. Adverse reactions were not associated with living FPLV vaccination, and FPLV did not interfere with simultaneous response to attenuated canine distemper virus.
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Schaller, G. (1990). Saving China's Wildlife. International Wildlife, 1(2), 30–41.
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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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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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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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Lutz, H., Hofmann-Lehmann, R., Fehr, D., Leutenegger, C., Hartmann, M., Ossent, P., et al. (1996). Liberation of the wilderness of wild felids bred under human custody: Danger of release of viral infections. Schweizer Archiv fuer Tierheilkunde, 138(12), 579–585.
Abstract: There are several felidae amongst the numerous endangered species. Means of aiding survival are the reintroduction to the wild of animals bred under the auspices of man and their relocation from densely populated to thinly populated areas. It is unlikely that the dangers of such reintroduction or relocation projects have been examined sufficiently in respect to the risks of virus infections confronting individuals kept in zoos or similar situations. This report presents infections may be expected to occur when relo- three examples to illustrate that accidental virus cating and reintroducing wild cats. The first example is the reintroduction of captive snow leopards. Zoo bred snow leopards may be infected with FIV, a virus infection that is highly unlikely to occur in the original hirnalayan highlands of Tibet and China. A second example is of several cases of FIP that occured in European wild cats bred in groups in captivity. The third example mentioned is the relocation of hons from East Africa where all the commonly known feline viruses are wide-spread to the Etosha National Park. In the latter, virus infections such as FIV, FCV and FPV do not occur. The indiscriminate relocation and reintroduction of the wild cats mentioned here harbours a potential of undesirable consequences.
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Chandra, S., & Laughlin, D. C. (1975). Virus-like particles in cystic mammary adenoma of a snow leopard. Cancer Res, 35(11 Pt 1), 3069–3074.
Abstract: Virus-like particles were observed in the giant cells of a mammary adenoma of a snow leopard kept in captivity. Particles that measured 115 to 125 nm in diameter budded from the lamella of endoplasmic reticulum and were studded on their inner surfaces with dense granules (approximately 12 nm) that gave them their unique ultrastructural morphology. Such particles were not observed extracellularly. Type B or type C particles were not seen in the tumor tissue.
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