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Tserendeleg, J. (1997). Status and Conservation of Snow Leopard in Mongolia. In R.Jackson, & A.Ahmad (Eds.), (pp. 42–47). Lahore, Pakistan: International Snow Leopard Trust.
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Schmidt, A. M., Hess, D. L., Schmidt, M. J., Smith, R. C., & Lewis, C. R. (1988). Serum concentrations of oestradiol and progesterone, and sexual behaviour during the normal oestrous cycle in the leopard (Panthera pardus) (Vol. 82).
Abstract: Three mature nulliparous female leopards were studied for 5 years. During three separate 6-month periods serum oestradiol and progesterone concentrations were measured at weekly intervals. Oestradiol was elevated over 21 pg/ml for 54 weeks during these 3 periods, and 36 oestradiol peaks (65\m=.\8\m=+-\6\m=.\3pg/ml (mean \m=+-\s.e.m.), range 21\p=n-\172pg/ml) were identified. Daily frequency of feline reproductive behaviours averaged over each week increased from 1\m=.\9\m=+-\0\m=.\2(n = 93) during weeks with low serum oestradiol concentrations (<21 pg/ml) to 5\m=.\3\m=+-\0\m=.\6(n = 54) during weeks when serum oestradiol concentrations (>21 pg/ml) were high. Increased serum progesterone concentrations (13\p=n-\98n/gml) were observed on 5 occasions in 2 leopards housed together. These presumptive luteal phases lasted from 1 to 5 weeks. Baseline progesterone values were 1\m=.\6\m=+-\0\m=.\4 ng/m(nl= 131). No progesterone increments were observed in isolated animals, and serum concentrations remained at baseline levels. These limited observations suggest that female leopards do not require intromission to induce ovulation and luteal function. The average interval between oestradiol peaks for cycles with no progesterone increment was 3\m=.\4weeks (range 1\p=n-\6weeks). The interval for the 3 complete cycles associated with elevated progesterone concentrations was 7\m=.\3weeks. Analysis of sexual behaviours over the 5-year study period revealed no evidence of seasonality in these
captive leopards.
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Sloane, A., Kelly, C., McDavitt, S., & Marples, N. (1998). Big cats in captivity: a quantitative analysis of enrichment. Adv.Etho, 33, 43.
Abstract: Studies on three species of big cats at Dublin Zoo have led to firm conclusions about the effects of certain forms of enrichment, some of which will be presented here. Lions, jaguars, and snow leopards were studied over two years and their behaviours quantified using focal animal sampling during selected hours during daylight. By comparison of these activity budgets with and without the enrichments being present, it was possible to identify the exact behavioural changes caused by each enrichment method, and to quantify these changes. In this contribution we present results showing that the presence of a platform in both lion and jaguar enclosures dramatically reduced stereotypic pacing behaviour. We will demonstrate that the effects of short term enrichment devices may have a wide range of effects on behaviours which outlast the presence of the stimulus. For instance scents added to the cage, or food/play items such as horse hides, hidden fish or ice-blocks often reduce pacing and increase resting later in the day, even after the cats have ceased using the enrichment items. This reduction in pacing and increase in resting time often meant that the amount of the enclosure used per hour was actually reduced with the presence of new stimuli, as result opposite to what might have been expected. The results of these studies will be discussed in relation to effective animal management.
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Bannikov A.G. (1973). Snow leopard (irbis). Felis uncia.
Abstract: Irbis is distributed in highlands of Kazakhstan, Kyrgyzstan, Tajikistan, and Altai. It preys mainly on wild sheep and ibex, marmots, pica, snow-cock, rarer other ungulates, rodents and birds. Sometimes it attacks domestic sheep. At the beginning of spring this species is on heat, gestation period being 90 100 days. Female bears two three (to five) cubs. The litter splits in one year. The animal sheds hair twice a year. It has a low population and therefore hunting for snow leopard is prohibited.
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Kuznetsnov, G. U., & Matyushkin, E. N. (1980). The snow leopard hunts. Int.Ped.Book of Snow Leopards, 11, 44–48.
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Shnitnikov V.N. (1936). Rocks and taluses. Snow leopard, Irbis Felis irbis Shreb.
Abstract: In Semerechie, snow leopard is not a rare species. In 1931, 53 snow leopards were hunted in southern Semerechie. In the past, at the markets of Central Tien Shan one could buy skins or live snow leopards, which were in demand abroad. Probably, number of snow leopards in Semerechie has increased. Now, it can be found not only in remote areas but in the vicinity of settlements (snow leopards, for instance, were observed some 20 30 km from Almaty, and 60 km from Frunze). Snow leopard preys mainly on ibex (¥…dr… sibiri¤…), snow-cock (O†traogallus himalauenses), and numerous argali – in some areas. The animal will never attack a man, even if wounded.
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Esipov A.V. (2004). Ugam Chatkal State Nature Park (Vol. N1).
Abstract: There are endangered species as bear, snow leopard and Menzbier's marmot recorded in Western Tien Shan mountains. Wild boar, Siberian ibex, roe deer, wolf, badger, porcupine and red fox are rather numerous species on this area.
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Ishunin G.I. (1989). The Felids family Felidae Gray, 1821.
Abstract: Zoolites of the Felidae family are known from the Upper Eocene Lower Pliocene in Eurasia, Africa, and North America. Two sub-families are know to inhabit the territory of the USSR and adjacent territories: the extinct sabre-toothed Felidae species Machairodontia and now existing Felidae species. In the USSR the extinct Felidae species were found to exist in Upper Miocene, Upper and Middle Pliocene, and Pleistocene. In Eurasia panthers has been know since early Pliocene. Three species were found in Uzbekistan – the extinct cave lion Felidae sd†l…†… (Goldfuss, 1810), and now existing P…nth†a… tigris, P…nth†a… pardus. The ancient finds and modern habitats are briefly described. Genus Uncia is represented by one species snow leopard or irbis. Probably it appeared in later Pliocene or Pleistocene in the mountain of Central Asia. In Uzbekistan, remains of snow leopard were found in the Samarqand region in the layer of Upper Pleistocene or Holocene. Probably it moved into the area in Pleistocene or the period of glacier removal in the Western Tien Shan mountains, Turkestan, Zeravshan, and Hissar ridges.
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Kydyraliev A.K. (1970). Some animal species' habitat alteration in the Central Tien Shan (Vol. Part 1.).
Abstract: Irrigation and drainage activity in Tien Shan led some bird species to disappear. Number of species to build their nests in tree holes has dropped. Mongolian sandpiper and black-bellied sand grouse disappeared in the steppe areas. Great bustard, formerly nesting in this area, can now be rarely seen only in migration. The direct anthropogenic influence resulted in shrinkage of game animal and bird populations such as moral, goitered gazelle, argali, snow leopard, and stone marten.
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Dang, H. (1967). The snow leopard and its prey. The Cheetal, 11, 47–58.
Abstract: Discusses distribution and habitat of snow leopard in India. Estimates population of 200-400 in entire Himalayan region. Reports seventeen occasions of observing snow leopards in the wild, one involving the killing of Himalayan thar. Discusses snow leopard hunting methods and food habits, and provides evidence of predation from examination of 17 snow leopard kills.
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