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Ganhar, J. (1979). The Wildlife of Ladakh. Srinagar, India: Haramukh Publications.
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Peters, G. (1980). The vocal repertoire of the snow leopard (Uncia uncia, Schreber 1775). In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 137–158). Helsinki: Helsinki Zoo.
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Freeman, H. (1990). The view from here: permit hunting of snow leopards. Snow Line, (Winter), 2–3.
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Korelov M.N. (1956). The vertebrates of Bostandyk region.
Abstract: Data about faunistic complexes of Bostandyk region is provided. Snow leopard inhabited in high mountains of Chatkal, Pskem and Ugam ridges. The tracks of irbis were recorded in the snowfield near the edge of Pskem ridge (upper Ichnach-say river).
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Murali, R., Redpath, S., Mishra, C. (2017). The value of ecosystem services in the high altitude Spiti Valley, Indian Trans-Himalaya. Elsevier, (28), 115–123.
Abstract: The high mountain ranges of South and Central Asia are increasingly being exposed to large-scale development
projects. These areas are home to traditional pastoralist communities and internationally important
biodiversity including the endangered snow leopard Panthera uncia. Development projects rely on
economic cost-benefit analysis, but the ecosystem services in the high Himalayas are poorly understood
and are rarely accounted for. As a first step to fill this gap, we identified the main ecosystem services used
by local people in the Trans-Himalayan Spiti Valley (7591 km2), a region important for conservation of
snow leopards and high mountain biodiversity, and undertook an economic valuation. Stakeholders identified
a range of services, though these were dominated by provisioning services identified by 90% of
respondents. Only 5.4% of the respondents recognised regulatory services and 4.8% recognised cultural
services. The mean economic value of provisioning services was estimated at US$ 3622 ± 149 HH1
yr1, which was 3.8 times higher than the average annual household income. Our results underscore
the need to account for ecosystem services in the cost-benefit analyses of large-scale development projects
in addition to assessments of their environmental and social impact.
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Jalanka, H. H., & Roeken, B. (1990). The use of Medetomidine, Medetomidine-Ketamine combinations, and Atipamezole in nondomestic mammals: A review. Journal-of-Zoo-and-Wildlife-Medicine, 21(3), 259–282.
Abstract: The recent development of potent and specifica lphar-adrenoceptoar gonistsa nd antagonists has enhanced their use in nondomestic animal immobilization and reversal. Medetomidine, a new potent alphar-agonist, in combination with the dissociative anesthetic ketamine, has been used to immobilize a variety of nondomestic mammals. Medetomidine alone induces sedation in a dose-dependent way, and complete immobilization has been achieved with high doses in semidomesticated reindeer (Rangifer tarandus) and blue foxes (Alopex lagopus). Howbver, we feel that ketamine should be added to the immobilization mixture to ensure complete immobilization and operator safety. In ketamine combinations, medetomidine doses are usually 60-100 pg/kg. The required ketamine doses are remarkably low:0.8-1.6 mglkg in most ruminants,2.5-3.0 mgUgin felids,u rsids,a nd canids,a nd 5.G-8.0m glkgi n primates,w olverines(Gulog ulo),ando therm uitelids. Clinically, the resulting immobilization is characterized by a smooth onset, good to excellent myorelaxation, and areflexia at higher doses. Determinations of hematologic, serum biochemicil, arterial blood gas,a nd acid-bases tatusp arametersi ndicate that the immobilization is physiologically sound. We have had no fatalities attributable to the immobilization mixture ( I ,240 immobilizations). The alphar-adrenoceptora ntagonist,a tipamezole,i s highly efective in reversingt he immobilization induced by medetomidine, medetomidine-ketamine combinations, or xylazine. In ruminants, the medetomidine-ketamine-induced immobilization can be rapidly and persistently reversed by administering 100-l 50 1rg/kg of alipamezole i.v. and the rest s.c., adjusting the total atipamezole dose to an atipamezole: medetomidine ratio of approximately 4-5 (w/w). Becauseth e required ketamine doses are relatively high in carnivores, we prefer to use a lower atipamezole dose (totil atipamezoie: medetomidine ratio approximately 2-3 w/w) and to administer it i.m. or s.c. Using thii regimen, reversals are calm and animals show minimal “residual ketamine effect.” Because atipamezole is a competitive antagonist, its dose should be reduced if it is administered late in the immobilization period when a large part of medetomidine has been endogenously metabolized. Xylazine-induced immobilization is rapidly reversed by I mg of atipamezole for every 8-12 mg of xylazine used.
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Tursunov Kh. (2003). The Ugam-Chatkal national park. The Chatkal state biosphere nature reserve.
Abstract: Established in 1990, the Ugam-Chatkal national park occupies an area of 668,350 ha and is the largest protected natural area in Uzbekistan. This area is famous for its rich species diversity. A number of rare and endangered plant and animal species, including among the others snow leopard, is found here. Being a core zone (strictly protected natural area), the Chatkal nature reserve is an integral part of the park. Snow leopard is periodically observed in the Tereksay river valley in the Maidantal area.
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Rodenburg, W. F. (1977). The Trade in Wild Animal Furs in Afghanistan.
Abstract: Estimated that 70-80 snow leopard pelts were traded annually at the Kabul bazaar.
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Johansson, O., Ausilio, G., Low, M., Lkhagvajav, P., Weckworth,
B., Sharma, K. (2020). The timing of breeding and independence for snow leopard females
and their cubs. Mammalian Biology, .
Abstract: Significant knowledge gaps persist on snow leopard demography
and reproductive behavior. From a GPS-collared population in Mongolia,
we estimated the timing of mating, parturition and independence. Based
on three mother–cub pairs, we describe the separation phase of the cub
from its mother as it gains independence. Snow leopards mated from
January–March and gave birth from April–June. Cubs remained with their
mother until their second winter (20–22 months of age) when cubs started
showing movements away from their mother for days at a time. This
initiation of independence appeared to coincide with their mother mating
with the territorial male. Two female cubs remained in their mothers’
territory for several months after initial separation, whereas the male
cub quickly dispersed. By comparing the relationship between body size
and age of independence across 11 solitary, medium-to-large felid
species, it was clear that snow leopards have a delayed timing of
separation compared to other species. We suggest this may be related to
their mating behavior and the difficulty of the habitat and prey capture
for juvenile snow leopards. Our results, while limited, provide
empirical estimates for understanding snow leopard ecology and for
parameterizing population models.
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San Antonio News. (1975). The story of the three little kittens. San Antonio News, I(6).
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