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Rieger, I. (1980). Some aspects of the history of ounce knowledge. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 2 (Vol. 2, pp. 1–36). Helsinki: Helsinki Zoo.
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Rieger, I. (1982). Breeding ounces, Uncia uncia (Schreber, 1775) in zoological gardens. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 49–50). Helsinki: Helsinki Zoo.
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Riordan, P. (1998). Unsupervised recognition of individual tigers and snow leopards from their footprints (Vol. 1).
Abstract: This study presents the testing of two unsupervised classification methods for their ability to accurately identify unknown individual tigers, Panthera tigris, and snow leopards, Panthera uncia, from their footprints. A neural-network based method, the Kohonen self-organizing map (SOM), and a Bayesian method, AutoClass, were assessed using hind footprints taken from captive animals under standardized conditions. AutoClass successfully discriminated individuals of both species from their footprints. Classification accuracy was greatest for tigers, with more misclassification of individuals occurring for snow leopards. Examination of variable influence on class formations failed to identify consistently influential measurements for either species. The self-organizing map did not provide accurate classification of individuals for either species. Results were not substantially improved by altering map dimensions nor by using principal components derived from the original data. The interpretation of resulting classifications and the importance of using such techniques in the study of wild animal populations are discussed. The need for further testing in the field is highlighted.
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Rishi, V. (1989). Snow leopards breed at Darjeeling Zoo. Zoo's Print, , 1–4.
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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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Ruedi, D., Heldstab, A., & van den Ingh, T. S. G. A. M. (1980). Liver cirrhosis in snow leopards – further results. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 195–204). Helsinki: Helsinki Zoo.
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Sangay, T., & Vernes, K. (2008). Human-wildlife conflict in the Kingdom of Bhutan: Patterns of livestock predation by large mammalian carnivores (Vol. 141).
Abstract: We examined predation activity throughout Bhutan by tiger (Panthera tigris), common leopard (Panthera pardus), snow leopard (Uncia uncia) and Himalayan black bear (Ursus thibetanus) on a variety of livestock types using data gathered over the first two years (2003-2005) of a compensation scheme for livestock losses. One thousand three hundred and seventy five kills were documented, with leopards killing significantly more livestock (70% of all kills),
than tigers (19%), bears (8%) and snow leopards (2%). About 50% of livestock killing were of cattle, and about 33% were of horses, with tigers, leopards and snow leopards killing a significantly greater proportion of horses than predicted from availability. Examination of cattle kills showed that leopards killed a significantly greater proportion of smaller prey (e.g., calves), whereas tigers killed a significantly greater proportion of larger prey (e.g., bulls). Overall, livestock predation was greatest in summer and autumn which corresponded with a peak in cropping agriculture; livestock are turned out to pasture and forest during the cropping season, and subsequently, are less well guarded than at other times. Across Bhutan, high horse density and low cattle and yak density were associated with high rates of livestock attack, but no relationship was found with forest cover or human population density. Several northern districts were identified as 'predation hotspots', where proportions of livestock lost to predation were considerable, and the ratio of reported kills to relative abundance of livestock was high. Implications of our findings for mitigating livestock losses and for conserving large carnivores in Bhutan are discussed.
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Schacter, A., Fitzgerald, K., & Doherty, J. (1980). Development of a snow leopard with and away from mother and siblings in the first six months. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 112–126). Helsinki: Helsinki Zoo.
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Shah, K. B. (1989). On a hunting pair of snow leopards in western Nepal. Journal of Bombay Natural Historical Society, 86, 236–237.
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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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