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Freeman, H. (1980). The snow leopard, today and yesterday. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 2 (Vol. 2, pp. 37–43). Helsinki: Helsinki Zoo.
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Freeman, H. (1980). Snow leopard: a cooperative study between zoos. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 127–136). Helsinki: Helsinki Zoo.
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Freeman, H. (1983). Behavior in adult pairs of captive snow leopards (Panthera uncia). Zoo Biology, 2(1), 1–22.
Abstract: Eight adult pairs of snow leopards (Panthera uncia) were observed for one to three years in the months December through March to determine the species' social and reproductive characteristics in captivity. To statistically examine the occurrence of behaviors as a function of estrus, the observation weeks were divided into three time blocks: before estrus, estrus, and after estrus. Using percentage of scan samples as an estimate of time spent in various behaviors, 16 behaviors and combined behavior categories were examined for (1) behaviors that differentiated successfully from unsuccessfully breeding pairs, (2) sex differences in behavior, (3) significant correlations between pair members, and (4) behaviors that showed time block effects. The rationale for identifying a behavioral profile of successful breeders in snow leopards was to aid zoos in their captive management programs by increasing their knowledge of the social behavior of this species. By finding correlates to breeding success, informed decisions on whether to change partners after a certain period of time, how to group the cats, and the optimum strategy for a survival plan can be made. (PsycINFO Database Record (c) 2000 APA, all rights reserved
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Frueh, R. (1968). A note on breeding snow leopards at the Saint Louis Zoo. Int.Zoo Yearbook, 8, 74–76.
Abstract: Breif comments on physical characteristics of the young, care and reproductive behavior of snow leopards
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Gaughan, M., & Doherty, J. (1982). Snow leopard rearing: Infant development with particular emphasis on play behaviour. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 121–126). Helsinki: Helsinki Zoo.
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Graham, L. H., Goodrowe, K. L., Raeside, J. I., & Liptrap, R. M. (1995). Non-invasive monitoring of ovarian function in several felid species by measurement of fecal estradiol-17-beta and progestins. Zoo Biology, 14(3), 223–237.
Abstract: An extraction and assay procedure to measure fecal estradiol-17-beta and progestin concentrations in several cat species was developed and validated for use for noninvasive monitoring of ovarian function. Fecal samples were collected over a range of 3-20 months from female tigers (three), lions (three), snow leopards (three), cheetahs (two), caracals (two), and domestic cats (five). Samples were extracted with 90% methanol, lipids removed with petroleum ether, and the estradiol and progestins in the methanol measured by radioimmunoassay (RIA). High Performance Liquid Chromatography (HPLC) fractionation and subsequent RIA of the fractions indicated that the estradiol-17-beta antiserum cross-reacted primarily with estradiol-17-beta in the feces of lions and tigers and was assumed to be specific for estradiol-17-beta in the feces of other species as well. However, there were several immunoreactive compounds, presumably progesterone metabolites, excreted in the feces which varied both quantitatively and qualitatively among species. The behavior of tigers, lions, cheetahs, and caracals was visually monitored during the collection period and frequency of sexual behaviors was positively correlated with increases in fecal estradiol in all species observed. The mean fecal estradiol-17-beta peaks were as follows: tigers, 128.0 +- 13.1; lions, 186.0 +- 14.8; snow leopards, 136.7 +- 15.9; cheetahs, 140.9 +- 9.0; caracals, 24.5 +- 4.0; and domestic cats 158.9 +- 19.3 ng/gm. Fecal progestin concentrations rose significantly (P lt 0,001) only after breeding or during pregnancy and were as follows: tigers, 5.6 +- 0.6; lions, 1.9 +- 0.1; cheetahs, 8.4 +- 1.1; and caracals, 2.4 +- 0.4 mu-g/gm. Fecal progestins were elevated for one-half to two-thirds of the gestation length during presumed pseudopregnancy but remained elevated throughout successful pregnancies. These results suggest that ovarian function can be monitored noninvasively in the family Felidae by the measurement of fecal estradiol-17-beta and progestin concentrations.
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Guerrero, D. (1998). Animal behavior concerns & solutions: snow leopard (Uncia uncia) evaluation, zoo. Anim.Keepers' Forum, 25(2), 56–58.
Abstract: The author offers advice on how a captive-raised snow leopard cub could be acclimated to humans so it could be used as a zoo “ambassador”. The cub had negative experiences with humans and lacked socialization with other animals and conspecifics. Methods of avoiding and redirecting the cub's aggressive behavior are suggested. lgh.
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Helman, R. G., Russell, W. C., Jenny, A., Miller, J., & Payeur, J. (1998). Diagnosis of tuberculosis in two snow leopards using polymerase chain reaction (Vol. 10).
Abstract: The incidence of tuberculosis in zoological animal collections is low, and the disease is monitored through skin testing primarily in primates and artiodactylids.15,16 Other exotic animals are clearly at risk; tuberculosis has been described in elephants (Mycobacterium tuberculosis, M. bovis), rhinoceros (M. bovis), felids (M. bovis), foxes (M. bovis), birds (M. avium complex, M. tuberculosis, M. bovis), and reptiles, amphibians, and fish (cryophilic Mycobacterium species). 1,2,4,6,8-10,13,14,17 Mycobacterial infections in mammals and birds serve as a potential source of disease that can spread to other animals and to humans.7,15,16 In humans, M. bovis and M. tuberculosis are the most important mycobacteria in the USA.
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Isenbugel, E., & Weilenmann, P. (1985). Colobomes of the Eyelid in an Ounce T (UNCIA-UNCIA, SCHREBER 1775) from the Zurich-Zoological-Garden. Praktische Tierarzt, 66(1), 61–62.
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Jackson, R. (1992). SSC Plan for Snow Leopard.
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