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Blomqvist, L. (1980). Distribution and Status of the Snow Leopard (Uncia uncia). Tiger Paper, Vii(4), 115–120.
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Blomqvist, L. (1984). Conservation Measurements taken for the Captive Snow Leopard, Panthera uncia, Population and a Report of Fluctuations in Stock in 1983. Int.Ped Book of Snow Leopards, 4, 55–71.
Abstract: Reports on conservation measures over the past 10 years. Notes current snow leopard exchange programs between zoos in the US and USSR and Europe. Describes status and reproductive success of the captive snow leopard population, list animals currently in captivity.
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Blomqvist, L. (1989). Captive Snow Leopard Report for 1989. International Zoo News, 265, 5–14.
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Blomqvist, L. (1995). Three decades of Snow Leopards Panthera uncia in Captivity. Int.Zoo Yearbook, 34, 178–185.
Abstract: The author reports the status of the captive population of snow leopards over the last three decades. Genetic and demographic information is also provided. The captive population as of 1992 was 541 leopards. klf. I
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Braden, K. (1982). The Geographical Distribution of the Snow Leopard in the USSR: Maps of Areas of Snow Leopard Habitation in the USSR. International Pedigree Book of Snow Leopards, 3, 25–39.
Abstract: Reviews published information from the USSR vs past status of the snow leopard in various parts of its range within that country. Maps provide locations in the USSR of evidence of snow leopard occurence from published records of the species over the last 100 yrs.
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Brown, J. L., Wasser, S. K., Wildt, D. E., & Graham, L. H. (1994). Comparative Aspects of Steroid Hormone Metabolism and Ovarian Activity in Felids, Measured Noninvasively in Feces. Biol Reprod, 51(4), 776–786.
Abstract: Noninvasive fecal assays were used to study steroid metabolism and ovarian activity in several felid species. Using the domestic cat (Felis catus) as model, the excretory products of injected [14C]estradiol (E2) and [14C]progesterone (P4) were determined. Within 2 days, 97.0 +/- 0.6% and 96.7 +/- 0.5% of recovered E2 and P4 radioactivity, respectively, was found in feces. E2 was excreted as unconjugated estradiol and estrone (40%) and as a non-enzyme- hydrolyzable conjugate (60%). P4 was excreted primarily as non-enzyme- hydrolyzable, conjugated metabolites (78%) and as unconjugated pregnenolone epimers. A simple method for extracting fecal steroid metabolites optimized extraction efficiencies of the E2 and P4 excretion products (90.1 +/- 0.8% and 87.2 +/- 1.4%, respectively). Analysis of HPLC fractions of extracted fecal samples from the radiolabel-injected domestic cats revealed that E2 immunoreactivity coincided primarily with the unconjugated metabolized [14C]E2 peak, whereas progestogen immunoreactivity coincided with a single conjugated epimer and multiple unconjugated pregnenolone epimers. After HPLC separation, similar immunoreactive E2 and P4 metabolite profiles were observed in the leopard cat (F. bengalensis), cheetah (Acinonyx jubatus), clouded leopard (Neofelis nebulosa), and snow leopard (Panthera uncia). Longitudinal analyses demonstrated that changes in fecal E2 and P4 metabolite concentrations reflected natural or artificially induced ovarian activity. For example, severalfold increases in E2 excretion were associated with overt estrus or exogenous gonadotropin treatment, and elevated fecal P4 metabolite concentrations occurred during pregnant and nonpregnant (pseudopregnant) luteal phases. Although overall concentrations were similar, the duration of elevated fecal P4 metabolites during pseudopregnancy was approximately half that observed during pregnancy. In summary, steroid metabolism mechanisms appear to be conserved among these physically diverse, taxonomically related species. Results indicate that this hormone-monitoring approach will be extremely useful for elucidating the hormonal regulatory mechanism associated with the reproductive cycle, pregnancy, and parturition of intractable and endangered felid species.
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Chakraborty, R. E., & Chakraborty, S. (1996). Identification of dorsal guard hairs of Indian species of the genus Panthera Oken (Carnivora: Felidae). Mammalia, 60(3), 480.
Abstract: Dorsal guard hairs of four living Indian species of the genus Panthera, viz. P. tigris, P. leo, P. pardus and P. uncia have been studied. It is found that the characters are somewhat overlapping, but identification of the species may be possible from the combination of characters.
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Chandra, S., & Laughlin, D. C. (1975). Virus-like particles in cystic mammary adenoma of a snow leopard. Cancer Res, 35(11 Pt 1), 3069–3074.
Abstract: Virus-like particles were observed in the giant cells of a mammary adenoma of a snow leopard kept in captivity. Particles that measured 115 to 125 nm in diameter budded from the lamella of endoplasmic reticulum and were studded on their inner surfaces with dense granules (approximately 12 nm) that gave them their unique ultrastructural morphology. Such particles were not observed extracellularly. Type B or type C particles were not seen in the tumor tissue.
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Clyde, V. L., Ramsay, E. C., & Bemis, D. A. (1997). Fecal shedding of Salmonella in exotic felids. J.Zoo Wildl.Med, 28(2), 148–152.
Abstract: The authors discuss the occurrence of salmonellosis in collections of exotic felids. Data suggest that zoo employees having contact with cat feces or raw diets have a high rate of occupational exposure to Salmonella and should exercise appropriate hygienic precautions. pcp
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Cunha, S. F. (1994). Summits, snow leopards, farmers, and fighters: Will politics prevent a national park in the high Pamirs of Tajikistan? Focus; New York, 44(1), 17–22.
Abstract: Tajikistan is the smallest, poorest and one of the most culturally diverse of the former Soviet Republics. The physical and cultural geography of the Pamir Mountains in Tajikistan are described, and recent legislative action taken to create a proposed park and civil strife that may stop the park's creation are discussed.
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