Heiz A.V. (1983). Snow leopard in Kyrgyzstan and its protection (Vol. 3).
Abstract: In the year 1970, the quantity of snow leopards in Kyrgyzstan was defined as 1,300 animals, while in the years to follow 1,600 animals were recorded. A snow leopard population has significantly decreased since recently because of intense extermination of snow leopard's prey ungulates, particularly ibex. In some areas of the Kyrgyz ridge livestock is growing in number thus affecting snow leopard population. It is extremely rare that snow leopard would attack livestock. Snow leopards can be caught under special license. Educational and awareness work among shepherds and hunters residing in the mountainous area of the country needs to be improved.
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Kuznetzov B.A. (1948). The cat family. The province of Central Asia mountains. The West Tien Shan area.
Abstract: It provides description of geographical distribution, habitats, behavior, and food of the cat family species in Kyrgyzstan (tiger, snow leopard, lynx, manul). It also provides zoogeographical description of Kyrgyzstan (zoogeographical zoning, landscape, fauna complexes), and zoning of Central Asia's mountainous areas. Snow leopard is met in the East Tien Shan, West Tien Shan, East Pamir, and Tajikistan mountainous areas. In Kyrgyzstan, snow leopard is distributed in highlands of the Talas Ala-Tau. Terskey Ala-Tau, Kyrgyz, Fergana, Alai and Zaalai ridges.
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Prokopov K.P. (1990). Taxonomic list of mammal fauna of eastern Kazakhstan (Vol. Vol. I.).
Abstract: During the period 1965 through 1988, studies were conducted in the north-east of Kazakhstan (Kazakhstan's Altai, Zaisan depression, Saur-Tarbagatai) and list of mammals (104 species) for the area made.
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Volozheninov N.N. (1986). Ecology of some mammals in western part of the Hissar ridge.
Abstract: Additional data on Lepus tolai, Ochotona rutila, Citellus relictus, Marmota caudata, Sus scrofa, Capra sibirica in western part of the Hissar ridge, Uzbekistan, is given here based on materials of the years 1978-1983. Information about distribution of these species, their numbers, food, enemies, and other ecologic issues is provided. Capra sibirica is a principle species snow leopard preys on. In 1899 1983, the authors recorded more than 20 cases of snow leopards' killing ibex of different ages.
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Jackson, R., Ahlborn, G., & Shah, K. B. (1990). Capture and Immobilization of wild snow leopards. Int.Ped.Book of Snow Leopards, 6, 93–102.
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Kolosov A.M. (1975). Central Asia.
Abstract: It describes a mammal species composition in the mountain ecosystems of Central Asia Kopetdag, Hissaro-Alai and Pamir, Tien Shan, and Tarbagatai ridge. Data on distribution and population number is presented.
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Wang, X., & Schaller, G. B. (1996). Status of large mammals in Western Inner Mongolia, China. Journal of East China Normal University (Special Issue of Zoology), , 93–104.
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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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Petzsch, H. (1969). Schneeleopard oder irbis, Uncia uncia (Schreber, 1775). (pp. 93–95).
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Kohli, K., Sankaran, M., Suryawanshi, K. R., Mishra, C. (2014). A penny saved is a penny earned: lean season foraging strategy of an alpine ungulate. Animal Behaviour, (92), 93–100.
Abstract: Lean season foraging strategies are critical for the survival of species inhabiting highly seasonal environments
such as alpine regions. However, inferring foraging strategies is often difficult because of
challenges associated with empirically estimating energetic costs and gains of foraging in the field. We
generated qualitative predictions for the relationship between daily winter foraging time, body size and
forage availability for three contrasting foraging strategies including time minimization, energy intake
maximization and net energy maximization. Our model predicts that for animals employing a time
minimization strategy, daily winter foraging time should not change with body size and should increase
with a reduction in forage availability. For energy intake maximization, foraging time should not vary
with either body size or forage availability. In contrast, for a net energy maximization strategy, foraging
time should decrease with increase in body size and with a reduction in forage availability. We contrasted
proportion of daily time spent foraging by bharal, Pseudois nayaur, a dimorphic grazer, across
different body size classes in two high-altitude sites differing in forage availability. Our results indicate
that bharal behave as net energy maximizers during winter. As predicted by the net energy maximization
strategy, daily winter foraging time of bharal declined with increasing body size, and was lower in the
site with low forage availability. Furthermore, as predicted by our model, foraging time declined as the
winter season progressed. We did not find support for the time minimizing or energy intake maximizing
strategies. Our qualitative model uses relative rather than absolute costs and gains of foraging which are
often difficult to estimate in the field. It thus offers a simple way to make informed inferences regarding
animal foraging strategies by contrasting estimates of daily foraging time across gradients of body size
and forage availability.
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