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Ruedi, D., Heldstab, A., Wiesner, H., & Keller, P. (1978). Liver cirrhosis in the snow leopard (Uncia uncia): Case histories of three animals and suggestion of some diagnostic possibilities. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 1 (Vol. 1, pp. 113–129). Helsinki: Helsinki Zoo.
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Schmidt, A. M., Hess, D. L., Schmidt, M. J., Smith, R. C., & Lewis, C. R. (1988). Serum concentrations of oestradiol and progesterone, and sexual behaviour during the normal oestrous cycle in the leopard (Panthera pardus) (Vol. 82).
Abstract: Three mature nulliparous female leopards were studied for 5 years. During three separate 6-month periods serum oestradiol and progesterone concentrations were measured at weekly intervals. Oestradiol was elevated over 21 pg/ml for 54 weeks during these 3 periods, and 36 oestradiol peaks (65\m=.\8\m=+-\6\m=.\3pg/ml (mean \m=+-\s.e.m.), range 21\p=n-\172pg/ml) were identified. Daily frequency of feline reproductive behaviours averaged over each week increased from 1\m=.\9\m=+-\0\m=.\2(n = 93) during weeks with low serum oestradiol concentrations (<21 pg/ml) to 5\m=.\3\m=+-\0\m=.\6(n = 54) during weeks when serum oestradiol concentrations (>21 pg/ml) were high. Increased serum progesterone concentrations (13\p=n-\98n/gml) were observed on 5 occasions in 2 leopards housed together. These presumptive luteal phases lasted from 1 to 5 weeks. Baseline progesterone values were 1\m=.\6\m=+-\0\m=.\4 ng/m(nl= 131). No progesterone increments were observed in isolated animals, and serum concentrations remained at baseline levels. These limited observations suggest that female leopards do not require intromission to induce ovulation and luteal function. The average interval between oestradiol peaks for cycles with no progesterone increment was 3\m=.\4weeks (range 1\p=n-\6weeks). The interval for the 3 complete cycles associated with elevated progesterone concentrations was 7\m=.\3weeks. Analysis of sexual behaviours over the 5-year study period revealed no evidence of seasonality in these
captive leopards.
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Slifka, K., Stacewicz-Sapuntzakis, S. M., Bowen, P., & Crissey, S. (1999). A Survey of Serum and Dietary Carotenoids in Captive Wild Animals. The Journal of Nutrition, 129, 380–390.
Abstract: Accumulation of carotenoids varies greatly among animal species and is not fully characterized.
Circulating carotenoid concentration data in captive wild animals are limited and may be useful for their management.
Serum carotenoid concentrations and dietary intakes were surveyed and the extent of accumulation
categorized for 76 species of captive wild animals at Brookfield Zoo. Blood samples were obtained opportunistically
from 275 individual animals immobilized for a variety of reasons; serum was analyzed for a- and b-carotene,
lutein 1 zeaxanthin, lycopene, b-cryptoxanthin and canthaxanthin. Total carotenoid content of diets was calculated
from tables and chemical analyses of commonly consumed dietary components. Diets were categorized as
low, moderate or high in carotenoid content as were total serum carotenoid concentrations. Animals were
classified as unknown, high, moderate or low (non-) accumulators of dietary cartenoids. Nonaccumulators had total
serum carotenoid concentrations of 0-101 nmol/L, whereas accumulators had concentrations that ranged widely,
from 225 to 35,351 nmol/L. Primates were uniquely distinguished by the widest range of type and concentration
of carotenoids in their sera. Most were classified as high to moderate accumulators. Felids had high accumulation
of b-carotene regardless of dietary intake, whereas a wide range of exotic birds accumulated only the xanthophylls,
lutein 1 zeaxanthin, canthaxanthin or cryptoxanthin. The exotic ungulates, with the exception of the bovids, had
negligible or nondetectable carotenoid serum concentrations despite moderate intakes. Bovids accumulated only
b-carotene despite moderately high lutein 1 zeaxanthin intakes. Wild captive species demonstrated a wide variety
of carotenoid accumulation patterns, which could be exploited to answer remaining questions concerning carotenoid
metabolism and function.
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Stidworthy, M. F., Lewis, J. C. M., Penderis, J., & Palmer, A. C. (2009). Progressive encephalomyelopathy and cerebellar degeneration in a captive-bred snow leopard (Uncia uncia) (Vol. 162).
Abstract: PROGRESSIVE encephalomyelopathy with cerebellar degeneration has been described in captive cheetahs (Palmer and others 2001) and in young domestic cats (Palmer and Cavanagh 1995). This case report describes the clinical and histopathological findings in a very similar condition affecting a young snow leopard (Uncia uncia) that had been born in a zoological park in eastern England as part of the globally coordinated breeding programme for this critically endangered species.
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Espinosa-Aviles, D., Taylor, M. L., Del Rocio Reyes-Montes, M., & Pe'rez-Torrez, A. (2008). Molecular findings of disseminated histoplasmosis in two captive snow leopards (Uncia uncia) (Vol. 39).
Abstract: This paper reports two cases of disseminated histoplasmosis in captive snow leopards (Uncia uncia). Histoplasmosis was diagnosed based on histopathology, immunohistochemistry, transmission electron microscopy, and molecular findings.
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Blomqvist, L. (1983). The 1982 international captive snow leopard report. Snow Line, 2, 1.
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Blomqvist, L. (1989). Status of the captive snow leopard (Panthera uncia) in 1987.
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Blomqvist, L. (1981). The 1980 annual report of the captive snow leopard (Panthera uncia) population and a review at the breeding results during the 1970's. Helsinki Zoo Annual Report. Helsinki: Helsinki Zoo.
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Blomqvist, L. (2003). Captive status of the snow leopard in Europe 2001 (Vol. 8).
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Blomqvist, L. (1980). The 1979 world register for the captive population of snow leopards, Panthera uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (pp. 62–75). Helsinki: Helsinki Zoo.
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