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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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Wharton, D., & Mainka, S. A. (1994). Captive Management of the Snow Leopard. In J.L.Fox, & D.Jizeng (Eds.), (pp. 135–148). Usa: Islt.
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Shuren, X. (1994). An introduction to feeding and management of snow leopard in Xining Zoo, China. In J.L.Fox, & D.Jizeng (Eds.), (pp. 177–182). Usa: Islt.
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Xinchun, M. (1994). Distribution in the wild and the captive raising of snow leopards in Xinjiang, China. In J.L.Fox, & D.Jizeng (Eds.), (pp. 157–162). Usa: Islt.
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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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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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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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Chakraborty, R. E., & Chakraborty, S. (1996). Identification of dorsal guard hairs of Indian species of the genus Panthera Oken (Carnivora: Felidae). Mammalia, 60(3), 480.
Abstract: Dorsal guard hairs of four living Indian species of the genus Panthera, viz. P. tigris, P. leo, P. pardus and P. uncia have been studied. It is found that the characters are somewhat overlapping, but identification of the species may be possible from the combination of characters.
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Jackson, R. M., Ahlborn, G., Gurung, M., & Ale, S. (1996). Reducing livestock depredation losses in the Nepalese Himalaya. Proc.Vertebr.Pest Conf, 17, 241–247.
Abstract: The authors investigated livestock depredation patterns of snow leopards on the northern slopes of the Himalayans near the villages of Manang and Khangshar, Nepal. Information is discussed on the relationships among livestock loss, endangered species management, public relations/conservation issues, and cooperative efforts among institutions involved in the decision making process. A plan is devised for alleviating livestock loss and protecting endangered species in the area. pcp
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Fox, J. L., & Chundawat, R. S. (1995). Wolves in the Transhimalayan region of India: The continued survival of a low-density population. Canadian Circumpolar Institute Occasional Publication No.35; Ecology and conservation of wolves in a changing world, 35, 95–103.
Abstract: Canadian Cirumpolar Institute, University of Alberta, Edmonton, Alberta, Canada/Second North American Symposium on Wolves, Edmonton, Alberta, Canada, August 25-27, 1992
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Jackson, R. (1994). Second SLIMS Workshop Held (Vol. xii). Seattle, WA: Islt.
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Oli, M. K. (1995). The Snow Leopard Dilema: Will they Persist. (pp. 433–441).
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Jackson, R. M. (1996). Home Range, Movements and Habitat use of Snow Leopard (Uncia uncia) in Nepal. Ph.D. thesis, University of London, University of London.
Abstract: Home ranges for five radio-tagged snow leopards (Uncia uncia) inhabiting prime habitat in Nepal Himalaya varied in size from 11-37 km2. These solitary felids were crepuscular in activity, and although highly mobile, nearly 90% of all consecutive day movements involved a straight line distance of 2km or less. No seasonal difference in daily movement or home range boundry was detected. While home ranges overlapped substancially, use of common core spaces was temporally seperated, with tagged animals being located 1.9 km or more apart during the smae day. Spatial analysis indicated that 47-55% of use occured within only 6-15% of total home area. The snow leopards shared a common core use area, which was located at a major stream confuence in an area where topography, habitat and prey abundance appeared to be more favorable. A young female used her core area least, a female with two cubs to the greatest extent. the core area was marked significantly more with scrapes, Faeces and other sighn than non-core sites, suggesting that social marking plays an important role in spacing individuals. Snow leopards showed a strong preference for bedding in steep, rocky or broken terrain, on or close to a natural vegetation or landform edge. linear landform features, such as a cliff or major ridgeline, were preferred for travelling and day time resting. This behavior would tend to place a snow leopard close to its preferred prey, blue sheep (Psuedois nayaur), which uses the same habitat at night. Marking was concetrated along commonly travelled routes, particularly river bluffs, cliff ledges and well defined ridgelines bordering stream confluences--features that were most abundant within the core area. Such marking may facilitate mutual avoidance, help maintain the species' solitary social structure, and also enable a relatively high density of snow leopard, especially within high-quality habitat.
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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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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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Wildt, D., Pukazhenthi, B., Brown, J., Monfort, S., Howard, J., & Roth, T. (1995). Spermatology for understanding, managing and conserving rare species. Reproduction Fertility and Development, 7(4), 811–824.
Abstract: Most conventional spermatology research involves common mammalian species including livestock, laboratory animals and humans. Yet, there are more than 4500 mammalian species inhabiting the planet for which little is known about basic reproductive biology, including sperm characteristics and function. This information is important, not just as adjunct knowledge, but because the majority of these species are threatened with extinction, largely due to human-induced pressures. The field of conservation is changing rapidly, and global cooperation is emerging among a variety of wildlife enthusiasts, ranging from management authorities of nature reserves to curators of rare zoological collections. Conservation progress depends on systematic, multidisciplinary research first to answer basic questions, with new data then applied to endangered species management plans. The reproductive physiologist is a crucial component of this scheme. Reproduction is the essence of species survival, and enormous effort needs to be directed at these 'untraditional' research species, subspecies and populations. Spermatology research combined with simultaneous efforts in endocrinology, embryology and cryopreservation (among others) can lead to the successful application of assisted reproduction. Examples from this laboratory include an array of wild felid species and a rare cervid and mustelid. Obstacles to success are formidable, including unique species-specificities, diminished genetic diversity and a general lack of resources. Nonetheless, the field offers tremendous opportunities for generating unique knowledge of comparative interest and with conservation utility.
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Graham, L. H., Goodrowe, K. L., Raeside, J. I., & Liptrap, R. M. (1995). Non-invasive monitoring of ovarian function in several felid species by measurement of fecal estradiol-17-beta and progestins. Zoo Biology, 14(3), 223–237.
Abstract: An extraction and assay procedure to measure fecal estradiol-17-beta and progestin concentrations in several cat species was developed and validated for use for noninvasive monitoring of ovarian function. Fecal samples were collected over a range of 3-20 months from female tigers (three), lions (three), snow leopards (three), cheetahs (two), caracals (two), and domestic cats (five). Samples were extracted with 90% methanol, lipids removed with petroleum ether, and the estradiol and progestins in the methanol measured by radioimmunoassay (RIA). High Performance Liquid Chromatography (HPLC) fractionation and subsequent RIA of the fractions indicated that the estradiol-17-beta antiserum cross-reacted primarily with estradiol-17-beta in the feces of lions and tigers and was assumed to be specific for estradiol-17-beta in the feces of other species as well. However, there were several immunoreactive compounds, presumably progesterone metabolites, excreted in the feces which varied both quantitatively and qualitatively among species. The behavior of tigers, lions, cheetahs, and caracals was visually monitored during the collection period and frequency of sexual behaviors was positively correlated with increases in fecal estradiol in all species observed. The mean fecal estradiol-17-beta peaks were as follows: tigers, 128.0 +- 13.1; lions, 186.0 +- 14.8; snow leopards, 136.7 +- 15.9; cheetahs, 140.9 +- 9.0; caracals, 24.5 +- 4.0; and domestic cats 158.9 +- 19.3 ng/gm. Fecal progestin concentrations rose significantly (P lt 0,001) only after breeding or during pregnancy and were as follows: tigers, 5.6 +- 0.6; lions, 1.9 +- 0.1; cheetahs, 8.4 +- 1.1; and caracals, 2.4 +- 0.4 mu-g/gm. Fecal progestins were elevated for one-half to two-thirds of the gestation length during presumed pseudopregnancy but remained elevated throughout successful pregnancies. These results suggest that ovarian function can be monitored noninvasively in the family Felidae by the measurement of fecal estradiol-17-beta and progestin concentrations.
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Scheber. (1975). Snow Leopard in the south part of Gobi-Altai mountain range.
Abstract: Accorfing to the information from Gurvan its rumored that the snow leopards grow in number and many times they attacked the livestock entering into the domestic area causing damage, we investigated theGurvan Tes sumon of Umnogobi aimag and also Noyon sumon todisplay the reserve review and spreading area of snow leopard from 22 of December of 1975 to 10th of January of 1976.
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Roth, T. L., Swanson, W. F., & Wildt, D. E. (1995). Snow leopard (Panthera unica) sperm longevity in vitro is not influenced by protein or energy source supplements but is affected by buffer source. Theriogenology, 43(1), 309.
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Jackson, R., & Hunter, D. O. (1995). Snow Leopard Survey and Conservation Handbook (2nd Edition). ISLT and National Biological Survey.
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Wikramanayake, E. D. (1995). Recommendations for Conservation Management of Jigme Dorji National Park.
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Anonymous. (1996). Trade continues in snow leopard skins. Snow Line, Xiv.
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Loginov, I., & Loginov, O. (1995). Elusive and Endangered:the snow leopard of Central Asia. Russian Conservation News, 4(August), 19–21.
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Koshkarev, E. (1996). The snow leopard in its northeastern range. Cat News, 25, 10.
Abstract: The author surveyed three sites in the central and eastern Sayan regions of Russia for snow leopards. In the Zhombolok River Basin of the Kropotkinskiy and Okinskiy Mountains, the author found seven snow leopard tracks, representing five or six individuals. In the Munku-Sardyk Peak area, one snow leopard track was found, and in the Tunkinskiy Ranffe area three tracks, representing at least two animals, were found. Other information is provided on local sightings. klf
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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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