International Snow Leopard Trust. (1999). International Snow Leopard Trust, Conservation and Education Program for 1999.
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Yongsheng, L. (1994). International hunting and the involvement of local people in Dulan, Qinghai, China. In J.L.Fox, & D.Jizeng (Eds.), (pp. 305–314). Usa: Islt.
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Rothschild, B. M., Rothschild, C., & Woods, R. J. (1998). Inflammatory arthritis in large cats: An expanded spectrum of spondyloarthropathy. Journal of Zoo and Wildlife Medicine, 29(3), 279–284.
Abstract: Spondyloarthropathy was documented for the first time in 14 (3.7%) of 386 large cats, affecting eight species belonging to three genera. The limited distribution of joint erosions, associated with spine and sacroiliac joint pathology, was indistinguishable from that occurring in humans with spondyloarthropathy of the reactive type. This form of inflammatory arthritis is almost twice as common as osteoarthritis (for felids as a whole), and animal well-being may be enhanced by its recognition and by initiation of specific treatment.
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Anonymous. Indian Wildlife Protection Act.
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Ishunin G.I. (1987). Genus Snow leopard Uncia gray, 1854.
Abstract: It provides data concerning biology, distribution and use game and commercial mammal species in Uzbekistan, and recommends on ways of hunting and initial fur-skin processing. It also describes the matter of conservation and rehabilitation of rare species' populations. From 1930-s to 1960-s over 20 snow leopard skins were reported to be traded officially.
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Bannikov A.G. (1971). Genus Panthera.
Abstract: It gives the description of genus Panthera: lion, tiger, leopard, jaguar and snow leopard. The mountains of Central Asia and South Siberia limit the habitat of snow leopard in the USSR. This species is also distributed in the Himalayas, Tibet, and mountains of Mongolia. In summer, it lives at 3,660 3,970 m above sea level, while in winter, following the ungulates; snow leopard descends to 1,800 m. In the Himalayas, it ascends up to 5,500 m above sea level in summer. In Djungar and Talas Ala-Tau, snow leopard keeps at 600 1,200 m. It takes refuge in caves and cracks of rocks. Snow leopard is mostly active in twilights and night, rarer in daylight, and preys on ungulates, hares, marmots, and others. The coupling period is winter or early spring. A gestation is about 90 days. It has 3 5 cubs in a litter.
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Epifanov V.M. (1968). Fauna.
Abstract: There are three fish species, two amphibian species, nine reptile, 97 bird species, and 23 mammal species, including snow leopard, in the Chatkal reserve. A list of animals and their brief description is provided.
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De Groot, H., Van Swieten, P., & Aalberse, R. C. (1990). Evidence for a Fel d I-like molecule in the “big cats” (Felidae species). J Allergy Clin Immunol, 86(1), 107–116.
Abstract: In this study, we investigated the cross-reactivity pattern of IgE and IgG4 antibodies to the major feline allergen, Fel d I. We studied the IgE and IgG4 response of 11 cat-allergic patients against Fel d I-like structures in eight members of the Felidae family: ocelot, puma, serval, siberian tiger, lion, jaguar, snow leopard, and caracal. Hair from these “big cats” was collected, extracted, and used in a RAST system and histamine-release test. By means of a RAST-inhibition assay with affinity-purified Fel d I from cat dander, it was established that, in the Felidae species, a Fel d I equivalent is present that reacts with IgE and IgG4 antibodies. We found that all patients had cross-reacting IgE antibodies to seven of the Felidae tested; no IgE antibodies reactive with the caracal were found. Eight of 10 patients with IgG4 antibodies directed to cat dander also had IgG4 antibodies directed to several Felidae species, including the caracal. However, the correlation between the IgE and the IgG4 antibody specificity was low, indicating that, in the case of Fel d I IgE and IgG4, antibodies do not necessarily have the same specificity.
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Poyarkov, A. D., Samoylova, G. S., & Subbotin, A. E. (2002). Evaluation of Potential Habitats of Snow Leopard (Uncia Uncia, Schreb.) In Altay-Khangay-Sayan Region and in Territory of Russian Federation: GIS Approach.. Islt: Islt.
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McCarthy, T. (2000). Ecology and Conservation of Snow Leopards, Gobi Brown Bears, and Wild Bactrian Camels in Mongolia. Ph.D. thesis, University of Massachusetts, Amherst, .
Abstract: Snow leopard ecology, distribution and abundance in Mongolia were studied between 1993 and 1999. I placed VHF and satellite radio-collars on 4 snow leopards, 2 males and 2 females, to determine home ranges, habitat use, movements, and activity. Home ranges of snow leopards in Mongolia were substantially larger than reported elsewhere. Males ranged over 61 – 142 km2 and female 58 to 1,590 km2. Cats had crepuscular activity patterns with daily movements averaging 5.1 km. Intraspecific distances averaged 1.3 km for males to 7.8 km for males. Leopards selected moderately to very-broken habitat with slopes > 20o, in areas containing ibex. Leopard distribution and abundance was determined using sign surveys. Leopard range in Mongolia is approximately 103,000 km2 but cats are not uniformly distributed within that range. High-density areas include the eastern and central Transaltai Gobi and the northern Altai ranges. Relative leopard densities compared well with relative ibex densities on a regional basis. A snow leopard conservation plan was drafted for Mongolia that identifies problems and threats, and provides an action plan. Wild Bactrian camels occur in the Great Gobi National Park (GGNP) and are thought to be declining due to low recruitment. I surveyed camels by jeep and at oases, observing 142 (4.2% young) and 183 (5.3% young) in 1997 and 1998. Current range was estimated at 33,300 km2. Some winter and calving ranges were recently abandoned. Track sizes and tooth ages from skulls were used to assess demographics. A deterministic model was produced that predicts camel extinction within 25 to 50 years under current recruitment rates and population estimates. Gobi brown bears are endemic to Mongolia and may number less than 35. Three population isolates may occur. I collected genetic material from bears at oases using hair traps. Microsatellite analyses of nuclear DNA determined sixteen unique genotypes, only two of which occurred at more than one oases. Genetic diversity was very low with expected heterozygosity = 0.32, and alleles per locus = 2.3. Mitochondrial DNA sequences were compared to other clades of brown bear and found to fall outside of all known lineages.
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