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Sitnikov, P. (1988). The Death of a Snow Leopard. In L.Blomqvist (Ed.), (pp. 7–8). Helsinki, Finland.
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Singh, J. (2002). Transboundary Stakeholders: Developing Cross-Border Conservation On Linkages for the Snow Leopard (Discussion Paper).. Islt: Islt.
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Shuren, X. (1994). An introduction to feeding and management of snow leopard in Xining Zoo, China. In J.L.Fox, & D.Jizeng (Eds.), (pp. 177–182). Usa: Islt.
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Shukurov E.J. (2004). List of of species included in Red data Book of Republic of Kyrgyzstan.
Abstract: It gives List of species included in Red data Book of Republic of Kyrgyzstan (1984). Totally 13 mammals including snow leopard listed in Kyrgyz Red data book.
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Shrestha, R., & Wegge, P. (2008). Habitat relationships between wild and domestic herbivores in Nepalese trans – Himalaya. Journal of Arid Environments, 72, 914–925.
Abstract: In the semi-arid ecosystems of Asia, where pastoralism is a main subsistence occupation, grazing competition from domestic stock is believed to displace the wild ungulates. We studied the habitat relationships among sympatric naur and domestic yak and smallstock in Phu valley in upper Manang district, Nepal, on the basis of their distribution on vegetation types, elevation and slope. To control for the disturbance effect by humans, we collected the data on naur from those ranges where domestic stock were not being attended by herders. We applied correspondence analysis to explore habitat associations among animal groups (n ¬ 1415) within and across-seasons. Within each association, interspecific habitat overlaps and species habitat preferences were calculated. Naur was strongly associated with free-ranging yak as they used similar altitudinal ranges in all seasons, except in spring. Their distributions on vegetation types and slopes were also quite similar, except for a stronger preference for alpine meadows by naur during summer and winter. Naur and smallstock did not form temporal associations as the latter consistently used lower elevations. In autumn and spring, however, naur spatially overlapped with the summer range of smallstock, and both preferred the alpine meadow habitat during these periods. Alpine meadow was the least abundant vegetation type but was consistently and preferentially used by all animal groups across seasons. At high stocking densities, all three animals groups are therefore likely to compete for this vegetation type. The role of spatio-temporal heterogeneity for interpreting the interspecific relationships among ungulates in the semi-arid rangelands of the trans-Himalaya is discussed.
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Shrestha, R., & Wegge, P. (2008). Wild sheep and livestock in Nepal Trans-Himalaya: coexistence or competition? Environmental Conservation, 32(2), 125–136.
Abstract: Excessive grazing by livestock is claimed to displace wild ungulates in the Trans-Himalaya. This study compares the seasonal diets and habitat use of sympatric wild naur Pseudois nayaur and domestic goat Capra hircus, sheep Ovis aries and free-ranging yak Bos grunniens in north Nepal and analyses their overlap both within and across seasons. Alpinemeadow and the legumes Oxytropis and Chesneya were critical resources for all animal groups. High overlap occurred cross-seasonally when smallstock (sheep and goats) in summer used the spring and autumn ranges of naur. Relatively high total ungulate biomass (3028 kg km-2) and low recruitment of naur (56 young per 100 adult females in autumn) suggested interspecific competition. The spatio-temporal heterogeneity in composition and phenology of food plants across the steep gradient of altitude, together with rotational grazing, appears to indirectly facilitate coexistence of naur and smallstock. However, owing to high crossseasonal (inter-seasonal) overlaps, competition is likely to occur between these two groups at high stocking densities. Within seasons, naur overlapped more with free-ranging yak than with smallstock. As their habitat use and diets were most similar in winter, when both fed extensively on the same species of shrubs, naur was most likely to compete with yak during that season.
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Shrestha, R., & Wegge, P. (2006). Determining the composition of herbivore diets in the Trans-Himalayan rangelands: A comparison of field methods. Journal of Rangeland Ecology and Management, 59(5), 512–518.
Abstract: In late summer, in a semi-arid mountain range in Nepal, we compared 3 field methods for determining the botanical composition of herbivore diets. Data were collected from the same animals belonging to 1 herd of domestic yak (Bos grunniens) and 2 herds of mixed smallstock, consisting of domestic goats (Capra hircus) and sheep (Ovis aries). Bite count, feeding site examination, and microhistological analysis of feces gave different estimates of forage categories and plant species in both animal groups. Because yaks grazed in other vegetation communities when not observed for bite-counts and feeding signs, the results from the latter methods could not be compared directly with that from fecal analysis. In smallstock, feeding site examination gave higher estimates of graminoids and lower estimates of shrubs than the other 2 methods, probably because all feeding signs on shrubs were not detected. Bite-counts and fecal analysis gave comparable results, except that forbs were underestimated by fecal analysis, presumably due to their more complete digestion. Owing to the difficulty in collecting samples that are representative of the entire grazing period and the problem of recording feeding signs correctly, both feeding site examination and bite-counts are unsuitable methods for studying the food habits of free ranging domestic and wild herbivores. Microhistological analysis of feces appears to be the most appropriate method, but correction factors are needed to adjust for differential digestion. The systematic use of photomicrographs improves the speed and accuracy of the fecal analysis.
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Shrestha, R., Wegge, P., & Koirala, R. A. (2005). Summer diets of wild and domestic ungulates in Nepal Himalaya. Journal of Zoology, 266, 111–119.
Abstract: The selection of summer forage by three sympatric ungulates in the Damodar Kunda region of upper Mustang in
north Nepal was studied to assess the extent of food overlap between them. To compare their diets, a microhistological technique of faecal analysis was used, adjusted for inherent biases by comparing it with bite-count data obtained in domestic goats. Tibetan argali Ovis ammon hodgsoni, naur (blue sheep or bharal) Pseudois nayaur and domestic goat Capra hircus consumed mostly forbs, graminoids and browse, respectively. The proportions of food items in their diets were significantly different both at the plant species (P<0.02) and at the forage category level (P<0.001). Except for sharing three common plants (Agrostis sp., Stipa sp. and Potentilla fruticosa), dietary overlap at the species level was quite low. At the forage category level, naur and domestic goat overlapped more than the other ungulate pairs. Although all three species were opportunistic, mixed feeders, argali was a more selective forb specialist grazer than the other two ungulates. Owing to some spatial separation and little dietary overlap, interspecific competition for summer forage was low. If animal densities increase, however, goats are expected to compete more with naur than with argali because of their more similar diets. Owing to differences in forage selection by argali and naur throughout their large geographical ranges, reflecting adaptations to local ecological conditions, inferences regarding forage competition between domestic livestock and these two wild caprins need to be made from local, site-specific studies, rather than from general diet comparisons.
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Shrestha, B. (2008). Prey Abundance and Prey Selection by Snow Leopard (uncia uncia) in the Sagarmatha (Mt. Everest) National Park, Nepal.
Abstract: Predators have significant ecological impacts on the region's prey-predator dynamic and community structure through their numbers and prey selection. During April-December 2007, I conducted a research in Sagarmatha (Mt. Everest) National Park (SNP) to: i) explore population status and density of wild prey species; Himalayan tahr, musk deer and game birds, ii) investigate diet of the snow leopard and to estimate prey selection by snow leopard, iii) identify the pattern of livestock depredation by snow leopard, its mitigation, and raise awareness through outreach program, and identify the challenge and opportunities on conservation snow leopard and its co-existence with wild ungulates and the human using the areas of the SNP. Methodology of my research included vantage points and regular monitoring from trails for Himalayan tahr, fixed line transect with belt drive method for musk deer and game birds, and microscopic hair identification in snow leopard's scat to investigate diet of snow leopard and to estimate prey selection. Based on available evidence and witness accounts of snow leopard attack on livestock, the patterns of livestock depredation were assessed. I obtained 201 sighting of Himalayan tahr (1760 individuals) and estimated 293 populations in post-parturient period (April-June), 394 in birth period (July -October) and 195 November- December) in rutting period. In average, ratio of male to females was ranged from 0.34 to 0.79 and ratio of kid to female was 0.21-0.35, and yearling to kid was 0.21- 0.47. The encounter rate for musk deer was 1.06 and density was 17.28/km2. For Himalayan monal, the encounter rate was 2.14 and density was 35.66/km2. I obtained 12 sighting of snow cock comprising 69 individual in Gokyo. The ratio of male to female was 1.18 and young to female was 2.18. Twelve species (8 species of wild and 4 species of domestic livestock) were identified in the 120 snow leopard scats examined. In average, snow leopard predated most frequently on Himalayan tahr and it was detected in 26.5% relative frequency of occurrence while occurred in 36.66% of all scats, then it was followed by musk deer (19.87%), yak (12.65%), cow (12.04%), dog (10.24%), unidentified mammal (3.61%), woolly hare (3.01%), rat sp. (2.4%), unidentified bird sp. (1.8%), pika (1.2%), and shrew (0.6%) (Table 5.8 ). Wild species were present in 58.99% of scats whereas domestic livestock with dog were present in 40.95% of scats. Snow leopard predated most frequently on wildlife species in three seasons; spring (61.62%), autumn (61.11%) and winter (65.51%), and most frequently on domestic species including dog in summer season (54.54%). In term of relative biomass consumed, in average, Himalayan tahr was the most important prey species contributed 26.27% of the biomass consumed. This was followed by yak (22.13%), cow (21.06%), musk deer (11.32%), horse (10.53%), wooly hare (1.09%), rat (0.29%), pika (0.14%) and shrew (0.07%). In average, domestic livestock including dog were contributed more biomass in the diet of snow leopard comprising 60.8% of the biomass consumed whilst the wild life species comprising 39.19%. The annual prey consumption by a snow leopard (based on 2 kg/day) was estimated to be three Himalayan tahr, seven musk deer, five wooly hare, four rat sp., two pika, one shrew and four livestock. In the present study, the highest frequency of attack was found during April to June and lowest to July to November. The day of rainy and cloudy was the more vulnerable to livestock depredation. Snow leopard attacks occurred were the highest at near escape cover such as shrub land and cliff. Both predation pressure on tahr and that on livestock suggest that the development of effective conservation strategies for two threatened species (predator and prey) depends on resolving conflicts between people and predators. Recently, direct control of free – ranging livestock, good husbandry and compensation to shepherds may reduce snow leopard – human conflict. In long term solution, the reintroduction of blue sheep at the higher altitudes could also “buffer” predation on livestock.
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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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