Jegal, A., Kashkarov, E., & Matyushkin E.N. (2010). Simple method to distinguish tracks of snow leopard and lynx.
Abstract: In the Mongolian and Gobi Altai mountain ranges and also in some other mountains in this region, the
distribution of the snow leopard and Eurasian lynx overlaps. In some cases, local hunters cannot
distinguish the tracks of both these animals. Therefore we outline a simple method to distinguish tracks of
the snow leopard and lynx.
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Jiang, Z. (2005). Snow leopards in the Dulan International Hunting Ground, Qinghai, China.
Abstract: From March to May, 2006œªwe conducted extensive snow leopard surveys in the Burhanbuda Mountain Kunlun Mountains, Qinghai Province, China. 32 linear transect of 5~15 km each, which running through each vegetation type, were surveyed within the study area. A total of 72 traces of snow leopard were found along 4 transects (12.5% of total transects). The traces included pug marks or footprints, scrapes and urine marks. We estimated the average density of wild ungulates in the region was 2.88ñ0.35 individuals km-2(n=29). We emplaced 16 auto2 trigger cameras in different environments and eight photos of snow leopard were shot by four cameras and the capture rate of snow leopard was 71.4%. The minimum snow leopard population size in the Burhanbuda Mountain was two, because two snow leopards were phototrapped by different cameras at almost same time. Simultaneously, the cameras also shot 63 photos of other wild animals, including five photos are unidentified wild animals, and 20 photos of livestock. We evaluated the human attitudes towards snow leopard by interviewing with 27 Tibetan householders of 30 householders live in the study area. We propose to establish a nature reserve for protecting and managing snow leopards in the region. Snow leopard (Uncia uncia) is considered as a unique species because it lives above the snow line, it is endemic to alpines in Central Asia, inhabiting in 12 countries across Central Asia (Fox, 1992). Snow leopard ranges in alpine areas in Qinghai, Xinjiang, Inner Mongolia, Tibet, Gansu and Sichuan in western China (Liao, 1985, 1986; Zhou, 1987; Ma et al., 2002; Jiang & Xu, 2006). The total population and habitat of snow leopards in China are estimated to be 2,000~2,500 individuals and 1,824,316 km2, only 5% of which is under the protection of nature reserves. The cat's current range is fragmented (Zou & Zheng, 2003). Due to strong human persecutions, populations of snow leopards decreased significantly since the end of the 20th century. Thus, the
snow leopards are under the protection of international and domestic laws. From March to May, 2006, we conducted two field surveys in Zhiyu Village, Dulan County in Burhanbuda Mountain, Kunlun Mountains, China to determine the population, distribution and survival status of snow leopards in the area. The aim of the study was to provide ecologic data for snow leopard conservation.
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Jie, Z., & Zongwei, W. (1963). Qinghai Fauna. Journal of Animal, 15(1), 125–137.
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Johnson, D. (1994). The National Fish and Wildlife Foundation goes international. Endangered Species Update, A, 11(10), A10.
Abstract: Abstract: The National Fish and Wildlife Foundation (NFWF) which is a conservation organization created in 1984 aims to conserve the species on an international context before they are endangered which will enable a more effective conservation procedure. The NFWF has addressed the causes of endangered species in India and South Asia such as the tiger, Indian wolf and the snow leopard and has supported the conservation efforts of the Siberian tiger. It has cooperated with multi-national organizations to evaluate the best strategy that could be adopted to prevent a future extinction of several species and has supported CITES programs
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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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Johnson, W. E., Eizirik, E., Pecon-Slattery, J., Murphy, W. J., Antunes, A., Teeling, E., et al. (2006). The Late Miocene Radiation of Modern Felidae: A Genetic Assessment (Vol. 311).
Abstract: Modern felid species descend from relatively recent (G11 million years ago) divergence and speciation events that produced successful predatory carnivores worldwide but that have confounded taxonomic classifications. A highly resolved molecular phylogeny with divergence dates for all living cat species, derived from autosomal, X-linked, Y-linked, and mitochondrial gene segments (22,789 base pairs) and 16 fossil calibrations define eight principal lineages produced through at least 10 intercontinental migrations facilitated by sea-level fluctuations. A ghost lineage analysis indicates that available felid fossils underestimate (i.e., unrepresented basal branch length) first occurrence by an average of 76%, revealing a low representation of felid lineages in paleontological remains. The phylogenetic performance of distinct gene classes showed that Y-chromosome segments are appreciably more informative than mitochondrial DNA, X-linked, or autosomal genes in resolving the rapid Felidae species radiation.
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Joslin, J. O., Garner, M., Collins, D., Kamaka, E., Sinabaldi, K., Meleo, K., et al. (2000). Viral papilloma and squamous cell carcinomas in snow leopards (Uncia uncia). In 2000 Proceedings AAZV & IAAAM Joint Conference (pp. 155–158). AAZV & IAAAM Joint Conference.
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Kamelin, R. V. (1990). Gissar Nature Reserve. The reserves in Middle Asia and Kazakstan. Moscow.
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Karesh, W. B., & Russell, R. (1988). Ovarian dysgerminoma in a snow leopard (Panthera uncia). Journal Of Zoo Animal Medicine, 19(4), 223–225.
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Karesh, W. B., & Asterino, R. (1988). Mandibular osteomyelitis in a snow leopard (Panthera-uncia) with a review of osteomyelitis in other species and man. Journal Of Zoo Animal Medicine, 19(3), 137–142.
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