Kashkarov D.N. (1923). Living conditions and living in various parts of the mountainous Turkestan. Central Asian snow leopard, irbis (Vol. Issue 2. The animals of mountainous Turkistan.).
Abstract: It describes fauna of the mountainous Turkestan. Irbis is met in Tien Shan, Pamir, Bukhara and Kopet-Dag. Apart from Turkistan, it lives in the Altai, Tibet and on northern slopes of the Himalayas. In Kopet-Dag, this species is met with another panther Caucasian leopard. It preys on ibex, wild sheep, roe deer, keklik (partridge), snow-cock and porcupine. It also attacks small livestock. Normally this species would never attack the man though hunters mentioned some cases that evidence otherwise.
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Kitchener, S. L., Meritt, & Rosenthal, M. (1975). Observations on the breeding and husbandry of snow leopards, Panthera uncia. Int.Zoo Yearbook, 15, 212–217.
Abstract: Describes adult care and breeding biology, and the care, growth, and mortality factors of young snow leopards in a successful breeding program in the Lincon Park Zoo, Chicago, Illinois.
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Jizeng, D., Ji-peng, J., Chang-xin, Z., & Freeman, H. (1994). Opening Remarks to Seventh International Snow Leopard Symposium. In J.L.Fox, & D.Jizeng (Eds.),. Usa: Islt.
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Kashkarov D.N. (1932). Order Carnivora- Carnivores. Family Felidae-Cats.
Abstract: Snow leopard inhabits Tien Shan, Pamir, Bukhara and possibly Kopet-dag, as well as the Altai, Tibet, and northern slopes of the Himalayas. It preys on ibex, wild sheep, roe deer, hare, keklik (partridge), snow-cock and porcupine and sometimes attacks livestock. Snow leopard is not considered a dangerous animal since even being wounded, it would escape from men and could only rush to the attack when deadlocked.
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Filla, M., Lama, R. P., Filla, T., Heurich, M., Balkenhol, N., Waltert, M., Khorozyan, I. (2022). Patterns of livestock depredation by snow leopards and effects of intervention strategies: lessons from the Nepalese Himalaya. Wildlife Research, .
Abstract: Context: Large carnivores are increasingly threatened by anthropogenic activities, and their protection is among the main goals of biodiversity conservation. The snow leopard (Panthera uncia) inhabits high-mountain landscapes where livestock depredation drives it into conflicts with local people and poses an obstacle for its conservation.
Aims: The aim of this study was to identify the livestock groups most vulnerable to depredation, target them in implementation of practical interventions, and assess the effectiveness of intervention strategies for conflict mitigation. We present a novel attempt to evaluate intervention strategies for particularly vulnerable species, age groups, time, and seasons.
Methods: In 2020, we conducted questionnaire surveys in two regions of the Annapurna Conservation Area, Nepal (Manang, n = 146 respondents and Upper Mustang, n = 183). We applied sample comparison testing, Jacobs’ selectivity index, and generalised linear models (GLMs) to assess rates and spatio-temporal heterogeneity of depredation, reveal vulnerable livestock groups, analyse potential effects of applied intervention strategies, and identify husbandry factors relevant to depredation.
Key results: Snow leopard predation was a major cause of livestock mortality in both regions (25.4–39.8%), resulting in an estimated annual loss of 3.2–3.6% of all livestock. The main intervention strategies (e.g. corrals during night-time and herding during daytime) were applied inconsistently and not associated with decreases in reported livestock losses. In contrast, we found some evidence that dogs, deterrents (light, music playing, flapping tape, and dung burning), and the use of multiple interventions were associated with a reduction in reported night-time depredation of yaks.
Conclusions and implications: We suggest conducting controlled randomised experiments for quantitative assessment of the effectiveness of dogs, deterrents, and the use of multiple interventions, and widely applying the most effective ones in local communities. This would benefit the long-term co-existence of snow leopards and humans in the Annapurna region and beyond.
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Blomqvist, L., & Sten, I. (1982). Reproductive biology of the snow leopard, Panthera uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (pp. 71–79). Helsinki: Helsinki Zoo.
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Razmakhnin V.E. (1977). Siberian wild ibex.
Abstract: It provides a detailed description of biology, distribution, geographic variability, behavior, and locomotion features of ibex in the USSR. Its population was defined as 100,000 animals, main enemies being wolf, snow leopard, and golden eagle. Wolf mainly preys on ibex at the end of winter; old males, weakened during the heat mostly becoming a prey. Snow leopards prey on ibexes all year round. Golden eagles mostly prey on young ibexes.
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Ishunin G.I. (1980). Snow leopard.
Abstract: In Uzbekistan, snow leopard is preserved along the Ugam, Pskem, Chatkal, Tirkestan, and Hissar ridges. Ibex is a main prey of the predator. It also preys on argali, wild boar, hares, roe-deers, rodents, kekliks (partridge), and rarely livestock. Catching the animals in the country is limited and exercised under special permissions.
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Aizin B.M. (1985). Snow leopard.
Abstract: Snow leopard is a rare and endangered species, distributed in all mountain ridges of Kyrgyzstan. Its population is 1,400 animals, density being 0.2 0.5 animal per 1,000 ha. Its population was noticed to decrease in some ridges because of decreasing populations of mountain ungulates. 200 snow leopards were caught for the purpose of zoo-export over the last 20 years. This species is protected in the nature reserves Sary Chelek, Besh Aral, and natural park Ala Archa.
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Roth, T. L., Swanson, W. F., Wildt, D. E., Collins, D., Burton, M., & Garell, D. M. (1996). Snow leopard (Panthera uncia) spermatozoa are sensitive to alkaline pH, but motility in vitro is not influenced by protein or energy supplements (Vol. 17).
Abstract: To better understand the biology of snow leopard spermatozoa and to facilitate developing assisted reproduction, a series of studies was conducted to: 1) identify the component(s) of complex culture media responsible for the detrimental effect on sperm survival in vitro, 2) optimize medium for supporting sperm viability, and 3) evaluate sperm capacitation in vitro. Constituents of complex media were added systematically to phosphate-buffered saline (PBS) to isolate the factor(s) influencing snow leopard sperm motility in vitro. Sperm capacitation was also assessed following incubation in PBS with bovine serum albumin (BSA), fetal calf serum (FCS), or heparin. For maintaining sperm motility, there was no benefit (P ? 0.05) to supplementing PBS with low (5%) or high (20%) concentrations of snow leopard serum (SLS) versus FCS or BSA. Likewise, adding supplemental energy substrates (pyruvate, glucose, lactate, or glutamine) did not enhance or hinder (P ? 0.05) sperm motility. However, motility rapidly decreased (P < 0.05) with the addition of NaHCO3 to PBS or Ham's F10 nutrient mixture. Surprisingly, Ham's F10 with no buffering component or with both NaHCO3 and N-Z-hydroxyethylpiperazine-N'-2- ethanesulfonic acid (HEPES) maintained sperm motility at levels similar (P ? 0.05) to PBS. Although sperm motility in all treatments decreased with time, there was a strong inverse relationship (P < 0.01; r = 0.90) between motility and sample pH at 6 hours. Spermatozoa incubated in PBS containing FCS, BSA, or heparin did not undergo the acrosome reaction when exposed to calcium ionophore. In summary, alkaline pH has a profound detrimental effect on snow leopard sperm motility, and capacitation does not occur under conditions that normally promote this event in other felid species. These results clearly demonstrate a high degree of interspecific variation among felids in fundamental sperm function, and they provide evidence for the necessity of basic research when developing assisted reproduction in little-studied nondomestic species.
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