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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Blomqvist, L. (2003). Captive status of the snow leopard in Europe 2001 (Vol. 8).
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Blomqvist, L. (2008). The status of the snow leopard in the EEP – program in 2007. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 9, pp. 20–24). Helsinki: Helsinki Zoo.
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Blower, J. H. (1986). Nature Conservation in Bhutan: Project Findings and Recommendations.
Abstract: Snow leopard is relatively common, but there is some destruction of its habitat in Northern Bhutan
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Bold, A., & Dorzhzunduy, S. (1976). Report on Snow Leopards in the Southern Spurs of the Gobi Altai. (Vol. 11, pp. 27–43).
Abstract: Estimates a population of 170-230 snow leopard within an area of 6600 km2 in Southern Gobi
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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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Braden, K. (1988). Snow leopard conservation in the USSR. Snow Line, Fall, 2.
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Broder, J., MacFadden, A., Cosens, L., Rosenstein, D., & Harrison, T. (2008). Use of Positive Reinforcement Conditioning to Monitor Pregnancy in an Unanesthetized Snow Leopard
(Uncia uncia) via Transabdominal Ultrasound (Vol. 27).
Abstract: Closely monitoring snow leopard (Uncia uncia) fetal developments via transabdominal ultrasound, with minimal stress to the animal, was the goal of this project. The staff at Potter Park Zoo has used the principles of habituation, desensitization, and positive reinforcement to train a female snow leopard (U. uncia). Ultrasound examinations were preformed on an unanesthetized feline at 63 and 84 days. The animal remained calm and compliant throughout both procedures. Fetuses were observed and measured on both occasions. The absence of anesthesia eliminated components of psychologic and physiologic stress associated with sedation. This was the first recorded instance of transabdominal ultrasound being carried out on an unanesthetized snow leopard. It documents the feasibility of detecting pregnancy and monitoring fetal development via ultrasound.
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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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