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Gromov I.M. (1963). Felis (Uncia) uncia Schreber (1776) leopard or irbis (Vol. Part.2.).
Abstract: An identification table for genus and species of mammals of USSR is given. The taxonomy, morphology, distribution and life history are described. The features of snow leopard Felis (Uncia) uncia, distribution, biology and practical value are described.
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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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Pollock, R. V., & Carmichael, L. E. (1983). Use of modified live feline panleukopenia virus vaccine to immunize dogs against canine parvovirus. Am J Vet Res, 44(2), 169–175.
Abstract: Modified live feline panleukopenia virus (FPLV) vaccine protected dogs against canine parvovirus (CPV) infection. However, unlike the long- lived (greater than or equal to 20-month) immunity engendered by CPV infection, the response of dogs to living FPLV was variable. Doses of FPLV (snow leopard strain) in excess of 10(5.7) TCID50 were necessary for uniform immunization; smaller inocula resulted in decreased success rates. The duration of immunity, as measured by the persistence of hemagglutination-inhibiting antibody, was related to the magnitude of the initial response to vaccination; dogs with vigorous initial responses resisted oronasal CPV challenge exposure 6 months after vaccination, and hemagglutination-inhibiting antibodies persisted in such dogs for greater than 1 year. Limited replication of FPLV in dogs was demonstrated, but unlike CPV, the feline virus did not spread to contact dogs or cats. Adverse reactions were not associated with living FPLV vaccination, and FPLV did not interfere with simultaneous response to attenuated canine distemper virus.
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Jackson, R., & Ahlborn, G. (1990). The role of protected areas in Nepal in maintaining viable populations of snow leopards. Int.Ped.Book of Snow Leopards, 6, 51–69.
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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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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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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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Chaudhuri, S., Mukherjee, S. K., Chatterjee, A., & Ganguli, J. L. (1992). Isolation of P multocida F-3, 4 from a stillborn snow leopard. Vet Rec, 130(2), 36.
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Thorel, M. F., Karoui, C., Varnerot, A., Fleury, C., & Vincent, V. (1998). Isolation of Mycobacterium bovis from baboons, leopards and a sea-lion. Vet Res, 29(2), 207–212.
Abstract: This study reports on two series of cases of Mycobacterium bovis infection in zoo animals. The first was in a captive population of baboons (Papio hamadryas) and the second in a mixed group of wild mammals, including four leopards (Panthera uncia and Panthera pardus) and a sea-lion (Otaria byrona). The isolation and identification of strains of M. bovis confirmed the presence of M. bovis infections in both zoos. The epidemiological study using genetic markers such as the IS6110-based DNA fingerprinting system made it possible to differentiate between M. bovis strains. The M. bovis strains isolated from baboons were shown to contain a single IS6110 copy, as usually do cattle isolates, whereas the M. bovis strains isolated from the other exotic animals presented multiple copies. This finding suggests that the origin of the contamination for the baboons in zoo A could be related to cattle. The origin of the contamination for the leopards and sea-lion in zoo B is more difficult to determine. In conclusion, the authors suggest some recommendations for avoiding outbreaks of tuberculosis infections in zoos.
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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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