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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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Buzurukov, A., & Muratov, R. (1994). Snow Leopard Conservation Tajikistan. In J.L.Fox, & D.Jizeng (Eds.), (pp. 29–32). Usa: Inst.
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Dhungel, S. (1994). Conservation of the Snow Leopard in Nepal. In J. L. Fox, & D. Jezing (Eds.), (pp. 47–50). Usa: Islt.
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Jackson, R., Zongyi, W., Xuedong, L., & Yun, C. (1994). Snow Leopards in the Qomolangma Nature Preserve of Tibet Autonomous Region. In J.L.Fox, & D.Jizeng (Eds.), (pp. 85–95). Usa: Islt.
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Harris, R. B. (1994). Dealing with uncertainty in counts of mountain ungulates. In J.L.Fox, & D. Jizeng (Eds.), (pp. 105–111). Usa: Islt.
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Harris, R. B. (1994). A note on snow leopards and local people in Nangqian County, Southern Qinghai Province. In J.L.Fox, & D. Jizeng (Eds.), (pp. 79–84). Usa: Islt.
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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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Jackson, R. M. (1996). Home Range, Movements and Habitat use of Snow Leopard (Uncia uncia) in Nepal. Ph.D. thesis, University of London, University of London.
Abstract: Home ranges for five radio-tagged snow leopards (Uncia uncia) inhabiting prime habitat in Nepal Himalaya varied in size from 11-37 km2. These solitary felids were crepuscular in activity, and although highly mobile, nearly 90% of all consecutive day movements involved a straight line distance of 2km or less. No seasonal difference in daily movement or home range boundry was detected. While home ranges overlapped substancially, use of common core spaces was temporally seperated, with tagged animals being located 1.9 km or more apart during the smae day. Spatial analysis indicated that 47-55% of use occured within only 6-15% of total home area. The snow leopards shared a common core use area, which was located at a major stream confuence in an area where topography, habitat and prey abundance appeared to be more favorable. A young female used her core area least, a female with two cubs to the greatest extent. the core area was marked significantly more with scrapes, Faeces and other sighn than non-core sites, suggesting that social marking plays an important role in spacing individuals. Snow leopards showed a strong preference for bedding in steep, rocky or broken terrain, on or close to a natural vegetation or landform edge. linear landform features, such as a cliff or major ridgeline, were preferred for travelling and day time resting. This behavior would tend to place a snow leopard close to its preferred prey, blue sheep (Psuedois nayaur), which uses the same habitat at night. Marking was concetrated along commonly travelled routes, particularly river bluffs, cliff ledges and well defined ridgelines bordering stream confluences--features that were most abundant within the core area. Such marking may facilitate mutual avoidance, help maintain the species' solitary social structure, and also enable a relatively high density of snow leopard, especially within high-quality habitat.
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Oli, M. K. (1996). Seasonal patterns in habitat use of blue sheep Pseudois nayaur (Artiodactyla, Bovidae) in Nepal. Mammalia, 60(2), 187–193.
Abstract: Blue sheep (Pseudois nayaur) are the main prey of the endangered snow leopard (Panthera uncia) as well as an important game species in Nepal. A knowledge of how blue sheep utilize their habitat is essential for the scientific management of the sheep and for the conservation of the snow leopard, but we only have a limited understanding of this aspect of blue sheep ecology. I studied the habitat use pattern of blue sheep by direct observation in the Anna-purna Conservation Area, Nepal where they occur sympatrically with the snow leopard. The sheep used grassland habitats more frequently during pre-parturition (spring) and post-parturition (autumn) than other habitat types, but scrub and grassland habitats were used equally frequently during the rut (winter). The sheep used smooth undulating slopes of medium steepness (<40 degrees) on southerly aspects within the elevation range of 4,200-4,600 m most frequently in all seasons, and there was no evidence of seasonal migration along the elevation gradient. When not in broken landforms (e.g., cliff, landslides), the sheep maintained proximity (less than or equal to 150 m) to such features suggesting their importance as escape cover (i.e., from predators). The use of habitat components by blue sheep appeared to be related to the distribution of foraging areas and escape cover.
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Oli, M. K., & Rogers, E. M. (1996). Seasonal pattern in group size and population composition of blue sheep in Manang, Nepal. Journal of Wildlife Management, 60(4), 797–801.
Abstract: Blue sheep (Pseudois nayaur) are the principal prey of the endangered snow leopard (Panthera uncia) in the Himalayas and adjacent ranges. We studied group size and population composition of blue sheep in Manang District, Annapurna Conservation Area, Nepal. Overall mean group size was 15.6 (SE = 1.3), but it varied seasonally (P lt 0.001), with significantly smaller groups in winter than in other seasons. Mixed groups were most numerous in all seasons, and there was no evidence of sexual segregation. Yearling sex ratio (93.7 M:100 F) did not vary seasonally, nor did the ratio deviate from parity. Adult sex ratio showed a seasonal pattern favoring males post-parturition but female-biased during the rut and pre-parturition. Seasonal variation in sex-specific mortality is offered as a plausible explanation for the observed pattern in adult sex ratio.
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