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Freeman, H., & Hutchins, M. (1978). Captive Management of Snow Leopard Cubs. Der Zoologischer Garten, 48, 49–62.
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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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Gaston, A. J., Garson, P. J., & Hunter, M. L. (1983). The status and conservation of forest wildlife in Himachal Pradesh, Western Himalayas. Biological Conservation, 27(4), 291–314.
Abstract: The wildlife of temperate forest ecosystems in the Western Himalayas is threatened by destruction of habitat and hunting. Two species of pheasants occuring in the survey area (western tragopan Tragopan melanocephalus and cheer pheasant Catreus wallichi) are listed in the IUCN Red Data Book (1979). Small populations of both species were located and information on their habitat requirements was obtained. The status of most large mammal species appears to be precarious, with the populations encountered being small and fragmented. Species formerly common but now rare include Himalayan brown bear Ursus arctos, Himalayan tahr Hemitragus jemlahicus and musk deer Moschus moschiferus. The snow leopard Panthera uncia has disappeared completely from the area.-from Authors
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Gee, E. P. (1967). Occurrence of the snow leopard Panthera uncia (Schreber) in Bhutan. Journal of the Natural History Museum Society, 30, 634–636.
Abstract: Indicates that snow leopard range includes all of Northern Bhutan
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Gosselin, S. J., Loudy, D. L., Tarr, M. J., Balistreri, W. F., Setchell, K. D., Johnston, J. O., et al. (1988). Veno-occlusive disease of the liver in captive cheetah. Vet Pathol, 25(1), 48–57.
Abstract: Liver tissues from 126 captive cheetah were evaluated by light microscopy and histochemistry; eight animals were evaluated by electron microscopy. The main hepatic lesion, a vascular lesion resembling veno- occlusive disease (VOD) of the liver and characterized by subendothelial fibrosis and proliferation of smooth muscle-like cells in the central veins, was seen in 60% of the sexually mature cheetah. Although this hepatic vascular lesion was seen in cheetah as young as 1 year of age, the most severe lesions, usually associated with liver failure, were found in cheetah between the ages of 6 and 11. There was no sex predisposition, and in approximately 40% of the VOD cases, liver disease was not suspected clinically or at necropsy. VOD was found in other felidae, especially in the snow leopard. High levels of vitamin A in livers, as well as in diets of the cheetah, could be a contributing factor in the development of VOD in some groups of cheetah.
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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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Hast, M. H. (1989). The larynx of roaring and non-roaring cats. J Anat, 163, 117–121.
Abstract: Dissections were made of the larynges of 14 species of the cat family, with representative specimens from all genera. It was found that the vocal folds of the larynx of genus Panthera (with the exception of the snow leopard) form the basic structure of a sound generator well- designed to produce a high acoustical energy. Combined with an efficient sound radiator (vocal tract) that can be adjusted in length, a Panthera can use its vocal instrument literally to blow its own horn with a 'roar'. Also, it is proposed that laryngeal morphology can be used as an anatomical character in mammalian taxonomy.
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Hast, M. H. (1989). The Larynx of Roaring and Non-Roaring Cats. The Journal of Anatomy, Summer.
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