Dawa, T., Farrington, J., Norbu, K. (2006). Human-wildlife Conflict in the Chang Tang Region of Tibet: The Impact of Tibetan Brown Bears and other Wildlife on Nomadic Herders with Recommendations for Conflict Mitigation. Lhasa, Tibet Autonomous Region, China: WWF China-Lhasa Field Office.
Abstract: The multiple-use Chang Tang and Seling Lake Nature Reserves were created in 1993 to protect the unique assemblage of large fauna inhabiting the high-altitude steppe grasslands of northern Tibet, including the Tibetan antelope, Tibetan wild ass, Tibetan brown bear, Tibetan Gazelle, wild yak, and snow leopard. Prior to creation of the reserve, many of these species were heavily hunted for meat and sale of parts. Since creation of the reserve, however, killing of wildlife by subsistence hunters and commercial poachers has declined while in the past five years a new problem has emerged, that of human-wildlife conflict. With human, livestock, and wildlife populations in the reserves all increasing, and animals apparently emboldened by reserve-wide hunting bans, all forms of human-wildlife conflict have surged rapidly since 2001. This conflict takes on four primary forms in the Chang Tang region: 1)killing of domestic livestock in corrals and on open pastures by Tibetan brown bears, snow leopards, and other predators, 2) Tibetan brown bears badly damaging herders’ cabins and tents in search of food, 3) loss of important grass resources to large herds of widely migrating wild ungulates, particularly the Tibetan wild ass, possibly leading to winter starvation of livestock, 4) driving off of domestic female yaks by wild yak bulls in search of harems.
In April of 2006, the authors conducted a wildlife conflict survey of 300 herding households in Nagchu Prefecture’s Shenzha, Tsonyi, and Nyima Counties. Results showed that the 87 percent of households had experienced some form of wildlife conflict since 1990. The Tibetan brown bear was the largest source of wildlife conflict, affecting 49 percent of surveyed households, followed by grazing competition conflict which affected 36 percent of surveyed households, and snow leopard conflict which affected 24 percent of surveyed households. Type and frequency of wildlife conflict problems cut across all three surveyed socio-economic factors, residence type, size of living group, and economic status/herd size, and was primarily a function of location. A break down of incidences of human-wildlife conflict into three 5 to 6-year time periods between January 1990 and April 2006 revealed dramatic increases in conflict occurring since 2001. When compared to the 1990-1995 period, the incidence of conflict today ranged from 2.6 times higher for fox conflict to 5.5 times higher for conflict with snow leopards, while there was a 4.6 fold increase in the occurrence of bear conflict. From second-hand accounts and wildlife remains confiscated from herders, it is now believed that retaliatory killing of wildlife rivals commercial poaching as the greatest threat to the continued existence of the Chang Tang region's large fauna. Human-wildlife conflict reduction strategies and wildlife conservation education programs must be devised and implemented in order to halt the retaliatory killing of wildlife by nomadic herders in the Chang Tang.
Lhasa, Tibet Autonomous Region, China: WWF China-Lhasa Field Office
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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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Weilemann P. (1982). Experiences in births of snow leopards in Zurich Zoo. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 111–116). Helsinki: Helsinki Zoo.
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Schacter, A., Fitzgerald, K., & Doherty, J. (1980). Development of a snow leopard with and away from mother and siblings in the first six months. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 112–126). Helsinki: Helsinki Zoo.
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Chundawat, R. S., Rodgers W.A., & Panwar, H. S. (1988). Status Report on Snow Leopard in India. In H.Freeman (Ed.), (pp. 113–120). Srinagar, India: International Snow Leopard Trust and Wildlife Institute of India.
Abstract: Gives status and distribution of snow leopards in India primarely based on sightings and kills.
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Hol, E. H., Marden, T. B., & Roelke, M. E. (1994). The importance of ecotoxicological research in management of the snow leopard: lessons learned from the Florida panther. In J.L.Fox and D.Jizeng (Ed.), (pp. 113–125). Usa: Islt.
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Ruedi, D., Heldstab, A., Wiesner, H., & Keller, P. (1978). Liver cirrhosis in the snow leopard (Uncia uncia): Case histories of three animals and suggestion of some diagnostic possibilities. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 1 (Vol. 1, pp. 113–129). Helsinki: Helsinki Zoo.
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Berezovikov N.N. (1990). The Markakol nature reserve.
Abstract: It provides general information about the Markakol nature reserve (Kazakhstan), physico-geographical characteristic, and description of flora and fauna. Snow leopards were noticed to enter the nature reserve from time to time, which seems to be very small for the predator to inhabit it permanently.
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Blomqvist, L. (1980). Distribution and Status of the Snow Leopard (Uncia uncia). Tiger Paper, Vii(4), 115–120.
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Flerov K.K. (1935). Capra sibirica, Uncia uncia uncia Erxleben.
Abstract: It describes identification signs of ibex and snow leopard; provides data concerning taxonomy, distribution and behavioral patterns of the both species. Snow leopard inhibits the mountains of Central Asia, Tarbagatai, Altai, Sayans and southward to the Humalayas. In Tajikistan snow leopard is distributed in Pamir, and probably, along alpine strip of the ridges in northern Tajikistan. The sub-species status is not defined. It is known that the same type inhabits the area from the Sayans to Himalayas. Only in Tibet and highlands of Sychuan and Gansu lives a well-marked sub-species Uncia uncia uncioides Hodgson.
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