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Schmidt, A. M., Hess, D. L., Schmidt, M. J., & Lewis, C. R. (1993). Serum concentrations of oestradiol and progesterone and frequency of sexual behaviour during the normal oestrous cycle in the snow leopard (Panthera uncia). J Reprod Fertil, 98(1), 91–95.
Abstract: Serum oestradiol and progesterone concentrations were measured at weekly intervals for six months, and correlated with daily behavioural observations in two adult female snow leopards (Panthera uncia). Three oestradiol peaks (> 21 pg ml-1; interval 3.6 weeks) were identified in a snow leopardess housed alone (two more were probably missed because of the weekly sampling schedule), and three oestradiol peaks were identified in a snow leopardess housed with a male as a breeding pair (interval 6 weeks). Daily frequencies of feline reproductive behaviour averaged 1.77 observations per observation period during weeks of high oestradiol and 0.62 during weeks of low oestradiol. Progesterone concentrations did not rise above baseline values (< 2 ng ml-1) in the isolated animal, but 6 weeks of high progesterone concentrations (4.9- 38.8 ng ml-1) was recorded in the paired snow leopardess following mating. No offspring were produced. Snow leopards were observed daily for an additional 4.5 years. Sexual behaviour peaks could be clearly identified from December through April, and average daily sexual behaviour scores were higher during these months than during the rest of the year. Intervals between sexual behaviour peaks for the isolated snow leopardess averaged 3.03 weeks. The sexual behaviour of the paired snow leopards decreased for 8-9 weeks following mating when no offspring were produced, and decreased for 13 weeks in one year when a single cub was born.
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Schmidt, R. E., Eisenbrandt, D. L., & Hubbard, G. B. (1984). Tyzzer's disease in snow leopards. J Comp Pathol, 94(1), 165–167.
Abstract: Tyzzer's disease was diagnosed histologically in 2 litters of newborn snow leopard kittens. The gross and histological lesions were similar to those reported in domestic cats and other animals. No signs of illness was noted in either of the snow leopard dams.
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Seidensticker, J., & Lumpkin, S. (1996). The adaptable leopard; unfortunately it's no match for modern man. Wildlife Conservation, 99(3), 52.
Abstract: Abstract: Leopards' adaptability has become the species' vulnerability. The animals do not hesitate to eat rotting flesh and will come back repeatedly to their meal, if disturbed. People have taken advantage of this by lacing carcasses with poison. Leopards are moderate in size compared to other cats, are stealthy and can live in areas as diverse as rain forests and deserts.
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Shafiq, M. M., & Abid, A. (1998). Status of large mammal species in Khunjerab National Park. Pakistan Journal of Forestry, 48(1-4), 91–96.
Abstract: Study on the current status of large mammals species population was carried out in Khunjerab National Park, Northern Areas. The observation recorded showed that the population of Tibetan Red fox (Vulpes vulpes montana), Snow leopard (Uncia uncia), and Wolf (Canis lupus) have, though a bit, increased but are still in the rank of “Endangered”. While the population of Himalyan Ibex (Cpara ibex sibirica) is increasing more rapidly and their status is now “Common” in the Park. The limited population of Marcopolo sheep (Ovis ammon polii), Tibetan wild Ass (Equus hemionus kiang) and Brown bear (Urus arctos) is still under threat, and comes them under “Critical Endangered” category.
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Shah, K. B. (1989). On a hunting pair of snow leopards in western Nepal. Journal of Bombay Natural Historical Society, 86, 236–237.
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Shang, Y. C. (1998). Behavioral Ecology. Beijing: Bejing University Press.
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Shi, K., Jun, Z. F. S., Zhigang, D., Riordan, P., & MacDonald, D. (2009). Reconfirmation of snow leopards in Taxkurgan Nature Reserve, Xinjiang, China. Oryx, 43(2), 169–170.
Abstract: China may hold a greater proportion of the global snow leopard Panthera uncia population than any other country, with the area of good quality suitable habitat, estimated at nearly 300,000 km2, comprising .50% of that available across the species' entire range. We can now reconfirm the presence of snow leopard in the Taxkurgan area of Xinjiang Province in north-west China after a period of 20 years.
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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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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, 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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