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Zhiryakov V.A. (1990). The Almaty nature reserve.
Abstract: It provides general information about the Almatya nature reserve (Kazakhstan), its physico-geographical features and description of flora and fauna. Snow leopard inhabits alpine zone and goes down as low as forest-meadow zone following ibex in winter. There are two or three families of snow leopard in the nature reserve. The population of ibex is 600 700 animals.
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Zhiryakov V.A. (2002). Ecology and behavior of the Snow leopard in Kazakhstan (Vol. N 1-4.).
Abstract: The data on spreading, numbers and population density of snow leopard in Kazakhstan are given in this article. The total number of the snow leopard in Kazakhstan is evaluated in 100-110 individuals. The everywhere occurred numbers' reduction under the influence of the anthropogenic factors is observed. The snow leopard' inhabitation area varies from 20 to 120 square kilometers depending on its regions. Sex and composition of the population and its aggregative behavior are given. The dynamics of numbers and mortality are estimated.
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Zhiryakov V.A. (1986). Snow leopard in the Almaty nature reserve. Short messages about snow leopards.
Abstract: Snow leopard is a common species for the Almaty nature reserve due to numerous wild ungulates, particularly ibexes (about 600 ibexes at a density of 32 animals per 1,000 ha) inhabiting the area. According to the data of 1982 there were 0.5 footprints of snow leopard per 10 km of transect. The remains of ibex, roe deer, squirrel, gray vole mouse and birds were found in faeces of snow leopards. Snow leopard attacks their prey unexpectedly, being in wait for it in such places where prey is difficult to escape from. When hunt is successful the prey is killed almost instantly. Snow leopard feeds upon the same prey for several days.
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Zimina R.P. (1964). Biology and biotopical distribution of mammals. Predators. Distribution of mammals by vertical zones.
Abstract: Fauna of the Issyk-Kul depression and the surrounding ridges consists of heterogeneous elements different in their ecologic features and origin. In highlands, more common are species of Central Asia's origin (gray marmot, snow leopard, dhole, ibex, argali, etc.). Snow leopard is met in Terskey-Alatau. Each year hunters catch/shoot one to three snow leopards in the Chon-Kizilsu river basin. In the Djeti-Oguz district, up to five eight snow leopards are caught each winter. Snow leopard is also caught/shot in the river basins Chon-Kizilsu, Karabatkak, Ortok, Archtor, Tekeletor, and Shatly.
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Zinchenko Yu.K. (1989). About characteristic of mammal fauna in the Markakol nature reserve (Vol. Part. II.).
Abstract: 50 mammal species permanently live in the nature reserve. There penetrate snow leopard, wolf, corsac, and wild boar on a relatively regular basis. Moral, roe deer, and elk migrate outside the Markakol depression in winter. Though mentioned in literature as species inhabiting the nature reserve, beaver, stone marten, and dhole are not met there today.
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Ming, M., Munkhtsog, B., McCarthy, T., McCarthy, K. (2011). Monitor ing of Population Density of Snow Leopard in X injiang. Journal of Ecology and Rural Environment, 27(1), 79–83.
Abstract: The snow leopard (Uncia uncia) is a very rare species in China. The survey of traces of snow leopard in Kunlun, Altay and Tianshan is them a instep of the Project of Snow Leopard in X injiang supported by the International Snow Leopard Trust ( SLT) and the Xinjiang Conservation Fund (XCF). During the field survey from 2004 to 2010, the Xinjiang Snow Leopard Group ( XSLG) spent about 270 days in over 20 different places, covering over 150 transects totaling nearly 190 km, and found 1- 3 traces per kilometer. The traces of snow leopard recorded include dung, odor, chains of footprints, scraping, paw nail marks, lying mark, fur, urine, bloodstain, leftover of prey corpse, roaring and others. Based on tracer image analyses, the XSLG got to know primarily scopes of the domains, distribution and relative density of the snow leopard in these areas. Then the group began to take infrared photos, conducted survey of food sources of the leopards, investigated fur market and paths of trading, and cases of killing, and carry out civil survey through questionnaire, non government organization community service and research on conflicts between grazing and wild life protection. A total of 36 infrared came ras were laid out, working a total of about 2 094 days or 50 256 hours. A total 71 rolls of film were collected and developed, includ ing 32 clear pictures of snow leopards, thus making up a shooting rate or capture rate of 1.53%. It was ascertained that in Tomur Peak area, there were 5- 8 snow leopards roaming within a range of 250 km2, forming a population density of 2��0- 3��2 per 100 km2. After compar ing the various monitoring results, the advantages and limitations of different monitoring methods have been discussed.
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Ale, S. B., Brown, J.S. (2009). Prey behavior leads to predator: a case study of the Himalayan tahr and the snow leopard in Sagarmatha (Mt. Everest) National Park, Nepal. Israel Journal of Ecology & Evolution, 55(4), 315–327.
Abstract: Rare, elusive predators offer few sightings, hindering research with small sample sizes and lack of experimentation. While predators may be elusive, their prey are more readily observed. Prey respond to the presence of a predator, and these fear responses may have population- and community-level consequences. Anti-predator behaviors, such as vigilance, allow us to sidestep the difficulty of direct field studies of large predators by studying them indirectly. Here we used a behavioral indicator, the vigilance behavior of the Himalayan tahr, the snow leopard’s main local prey, to reveal the distribution and habitat use of snow leopards in the Mt. Everest region of Nepal. We combined techniques of conventional field biology with concepts of foraging theory to study prey behavior in order to obtain insights into the predator’s ecology. The Himalayan tahr’s vigilance behavior correlates with the distribution of snow leopard signs. Tahr actually led us to six sightings of snow leopards. We conclude that behavioral indicators provided by prey offer a valuable tool for studying and monitoring stealthy and rare carnivores.
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Ale, S. B., Boesi, R. (2005). Snow Leopard Sightings on the Top of the World. Cat News, (43), 19–20.
Abstract: Sightings of snow leopards Uncia uncia in the wild are rare. This is because snow leopards occur in low numbers and are very elusive (Schaller 1977). Snow leopards may be sparsely distributed,but they may not, however, be very elusive in the world's highest park, Sagarmatha (Mt. Everest) National Park (86° 30' 53“ E to 86° 99' 08” E and 27° 46' 19“ N to 27° 06' 45” N) in Nepal.
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Chapron, G. (2005). Re-wilding: other projects help carnivores stay wild. Nature, 437, 318.
Abstract: Letter to Nature Editor, in response to: In their plea for bringing Pleistocene wildlife to the New World (“Re-wilding North America” Nature 436, 913–914; 2005), Josh Donlan and colleagues do not discuss successful efforts to ensure long-term survival of large carnivores in Africa and Asia. A few examples are given.
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Christiansen, P. (2007). Canine morphology in the larger Felidae: implications for feeding ecology. Biological Journal of the Linnean Society, 91, 573–592.
Abstract: Canine morphology is analysed at seven intervals along the crown in both
anteroposterior and lateromedial perspective in seven species of large felids. The puma and the snow leopard have stout, rather conical canines, whereas those of lions, jaguars, and tigers bear substantial resemblance to each other, reflecting their phylogenetic relationships, and are less conical and large. The canines of the leopard are intermediate in morphology between those of the other species, probably reflecting its more generalized diet. The clouded leopard has very large and blade-like canines, which are different from the other analysed species. Canine bending strengths to estimated bite forces appear to differ less among the species than morphology,indicating that the evolution of canines has been constricted with respect to their strength in failure, probably owing to their being equally important for species fitness. However, the clouded leopard again stands out, having a high estimated bite force and rather weak canines in bending about the anteroposterior as well as lateromedial planes compared to the other species. Canine morphology to some extent reflects differences in killing mode, but also appears to be related to the phylogeny. The marked divergence of the clouded leopard is presently not understood.
Keywords: bite force, canine, clouded leopard, feeding behaviour, felid, Homotherium serum, leopard, Megantereoncultridens, morphology, Neofelis nebulosa, paleontology, Panthera pardus, Panthera tigris, puma, Puma concolor, Smilodon fatalis, Smilodon populator, snow leopard, Uncia uncia
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