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Marma B.B.and Yunchis V.V. (1968). A contribution to biology of the Snow-leopard (Panthera uncia uncia) (by observations in captivity) (Vol. XLVII, issue 11.).
Abstract: The methods to obtain the progeny of the snow leopard (Panthera uncia uncia) in captivity were being elaborated in the zoological garden of Kaunas, Lithuanian SSR. The blood characteristics for snow leopards is given and compared to that for African lions and Sumatrian tigers. A series of internal, external and clinical indices is established. The rat lasts for 5-7 day, the duration of pregnancy equals 98 days. The duration of lactation varies from 3 to 4 months. Sexual maturity is attained on the 3rd-4th year. From 1960 to 1967 in zoological garden of the world about 29 snow leopards were born, 14 of them in the Kaunas zoological garden.
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Lu, Q., Xiao, L., Cheng, C., Lu, Z., Zhao, J., Yao, M. (2021). Snow Leopard Dietary Preferences and Livestock Predation Revealed by Fecal DNA Metabarcoding: No Evidence for Apparent Competition Between Wild and Domestic Prey. Frontiers in Ecology and Evolution, 9(783546), 1–14.
Abstract: Accurate assessments of the patterns and drivers of livestock depredation by wild carnivores are vital for designing effective mitigation strategies to reduce human-wildlife conflict. Snow leopard’s (Panthera uncia) range extensively overlaps pastoralist land- use and livestock predation there is widely reported, but the ecological determinants of livestock consumption by snow leopards remain obscure. We investigated snow leopard dietary habits at seven sites across the Sanjiangyuan region of the Qinghai– Tibetan Plateau (QTP), an area central to the species’ global range. Snow leopard abundance, wild prey composition, and livestock density varied among those sites, thus allowing us to test the effects of various factors on snow leopard diet and livestock predation. Using DNA metabarcoding, we obtained highly resolved dietary data from 351 genetically verified snow leopard fecal samples. We then analyzed the prey preferences of snow leopards and examined ecological factors related to their livestock consumption. Across the sites, snow leopard prey was composed mainly of wild ungulates (mean = 81.5% of dietary sequences), particularly bharal (Pseudois nayaur), and supplemented with livestock (7.62%) and smaller mammals (marmots, pikas, mice; 10.7%). Snow leopards showed a strong preference for bharal, relative to livestock, based on their densities. Interestingly, both proportional and total livestock consumption by snow leopards increased linearly with local livestock biomass, but not with livestock density. That, together with a slight negative relationship with bharal density, supports apparent facilitation between wild and domestic prey. We also found a significant positive correlation between population densities of snow leopard and bharal, yet those densities showed slight negative relationships with livestock density. Our results highlight the importance of sufficient wild ungulate abundance to the conservation of viable snow leopard populations. Additionally, livestock protection is critically needed to reduce losses to snow leopard depredation, especially where local livestock abundances are high.
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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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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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Ale, S., & Brown, J. (2007). The contingencies of group size and vigilance (Vol. 9).
Abstract: Background: Predation risk declines non-linearly with one's own vigilance and the vigilance of others in the group (the 'many-eyes' effect). Furthermore, as group size increases, the individual's risk of predation may decline through dilution with more potential victims, but may increase if larger groups attract more predators. These are known, respectively, as the dilution effect and the attraction effect.
Assumptions: Feeding animals use vigilance to trade-off food and safety. Net feeding rate declines linearly with vigilance.
Question: How do the many-eyes, dilution, and attraction effects interact to influence the relationship between group size and vigilance behaviour?
Mathematical methods: We use game theory and the fitness-generating function to determine the ESS level of vigilance of an individual within a group.
Predictions: Vigilance decreases with group size as a consequence of the many-eyes and dilution effects but increases with group size as a consequence of the attraction effect, when they act independent of each other. Their synergetic effects on vigilance depend upon the relative strengths of each and their interactions. Regardless, the influence of other factors on vigilance – such as encounter rate with predators, predator lethality, marginal value of energy, and value of vigilance – decline with group size.
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Lilin, Z. (1994). Captive rearing of a wild snow leopard cub in the Xining Zoo, China. In J.L.Fox, & D.Jizeng (Eds.), (pp. 177–182). Usa: Islt.
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Hongguang, H., & Yongfu, X. (1994). Captive snow leopards in the Chongqing Zoo. In J.L.Fox, & D.Jizeng (Eds.), (pp. 191–193). Usa: Islt.
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Fox, J. L., & Chundawat, R. S. (1988). Observations of snow leopard stalking, killing and feeding behavior. Mammalia, 52(1), 137–140.
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Brunstein, L. (1978). Handrearing Snow Leopards in the Cheyenne Mountain Zoo. Int.Ped.Book of Snow Leopards, 1, 44–49.
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Aromov B. (1995). The Biology of the Snow Leopard in the Hissar Nature Reserve.
Abstract: The work contains data on biology snow leopard in Hissar nature reserve, Uzbekistan. The number of snow leopards in this reserve has increased from two or four in 1981 to between 13 and 17 individuals in 1994. Since 1981, snow leopards have been sighted 72 times and their tracks or pugmarks 223 times. In the Hissar Nature Reserve snow leopards largely feed on ibex. Over a period of 14 years, 92 kills and remains of ibex aged from one to thirteen years of age have been examined. Other records of predation, by the number of events observed, include 33 cases of juvenile and mature horses, 25 long-tailed marmot (Marmota caudata). 18 Himalayan snowcock (Tetraogallus himalayemis), 17 domestic goat, 13 wild boar (Sus scrofa), five domestic sheep and three incidents involving cattle. Twenty-two attacks on domestic flocks were reported, and these occurred during both the daytime and at night. Snow leopards usually mate between the 20th of February and March 20th. The offspring are born in late April to May, and there are usually two per litter (23 encounters), although a single litter of three has also been recorded.
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