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Ishunin G.I. (1987). Genus Snow leopard Uncia gray, 1854.
Abstract: It provides data concerning biology, distribution and use game and commercial mammal species in Uzbekistan, and recommends on ways of hunting and initial fur-skin processing. It also describes the matter of conservation and rehabilitation of rare species' populations. From 1930-s to 1960-s over 20 snow leopard skins were reported to be traded officially.
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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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De-hao, L. (1989). Economic Fauna of Qinghai. Xining: Qinghai People's Publishing House.
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Kreuzberg-Mukhina, E., Esipov A.V., Bykova, E. A., Vashetko, E. V., & Aromov, B. (2003). Development of the national Action Plan for the conservation of Snow Leopard in Uzbekistan. Report: 1-51 (Vol. 1-51). Uzbekistan.
Abstract: This document is the final report on the ISLT Project “Development of national Action plan for the conservation of Snow Leopard in Uzbekistan” and a Conservation Strategy for the Snow leopard in Uzbekistan. It includes biology and current status, limiting factors, existing and necessary conservation measures.
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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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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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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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Jackson, R. (1992). SSC Plan for Snow Leopard.
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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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