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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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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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Meklenburtsev R.N. (1949). About ecology of ibex in Pamir (Vol. Vol. 28, edition 5.).
Abstract: Ibex is distributed all over the Pamir mountains, inhabiting rocks and canyons and ascending up to 5,500 m above sea level. In summer, ibex mostly feeds upon sedge and cereals, in winter wormwood. It keeps in herds containing 15 to 30 animals. The coupling period is December; kids being born at the beginning of June. The most dangerous predators are snow leopard and wolf. Ibex is a main commercial game species.
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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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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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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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Ognev S.I. (1935). Uncia uncia Sch., 1778. Irbis or snow leopard (Vol. Vol.3.).
Abstract: It describes identification signs and taxonomy of genus Uncia Gray and the only representative of genus Uncia uncia Sch., 1778, distribution and some features of the species' biology. A habitat of snow leopard includes the mountains of Central Asia from Kopet-Dag and northern Iran to the east along the mountain systems of Pamir, Turkestan, Gilgit, Tibet, Himalayas before the country Kam. On the north, snow leopard is met in Tarbagatai, Altai, Sayans, and further eastward to the Yablonoviy and Stanovoy ridges reaching the confluence of the Shilka and Argun rivers.
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Sludsky A.A. (1982). Genus Snow leopard Uncia Gray, 1854. Snow leopard Uncia uncia Schreber, 1775 (Vol. Vol. III, Part 2.).
Abstract: Snow leopard is rare and extinctive species that have scientific and aesthetic significance. The features of genus Uncia and species Uncia uncia are described. Also distribution, habitat, way of life, reproduction biology, behavioural patterns, migration routes, infections and parasites, enemies and competitors, number and number fluctuation, practical value of snow leopard in the Kazakhstan are given.
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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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