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Rishi, V. (1989). Snow leopards breed at Darjeeling Zoo. Zoo's Print, , 1–4.
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Roth, T. L., Swanson, W. F., & Wildt, D. E. (1995). Snow leopard (Panthera unica) sperm longevity in vitro is not influenced by protein or energy source supplements but is affected by buffer source. Theriogenology, 43(1), 309.
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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, R. E., Eisenbrandt, D. L., & Hubbard, G. B. (1984). Tyzzer's disease in snow leopards. J Comp Pathol, 94(1), 165–167.
Abstract: Tyzzer's disease was diagnosed histologically in 2 litters of newborn snow leopard kittens. The gross and histological lesions were similar to those reported in domestic cats and other animals. No signs of illness was noted in either of the snow leopard dams.
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Schmidt, A. M., Hess, D. L., Schmidt, M. J., & Lewis, C. R. (1993). Serum concentrations of oestradiol and progesterone and frequency of sexual behaviour during the normal oestrous cycle in the snow leopard (Panthera uncia). J Reprod Fertil, 98(1), 91–95.
Abstract: Serum oestradiol and progesterone concentrations were measured at weekly intervals for six months, and correlated with daily behavioural observations in two adult female snow leopards (Panthera uncia). Three oestradiol peaks (> 21 pg ml-1; interval 3.6 weeks) were identified in a snow leopardess housed alone (two more were probably missed because of the weekly sampling schedule), and three oestradiol peaks were identified in a snow leopardess housed with a male as a breeding pair (interval 6 weeks). Daily frequencies of feline reproductive behaviour averaged 1.77 observations per observation period during weeks of high oestradiol and 0.62 during weeks of low oestradiol. Progesterone concentrations did not rise above baseline values (< 2 ng ml-1) in the isolated animal, but 6 weeks of high progesterone concentrations (4.9- 38.8 ng ml-1) was recorded in the paired snow leopardess following mating. No offspring were produced. Snow leopards were observed daily for an additional 4.5 years. Sexual behaviour peaks could be clearly identified from December through April, and average daily sexual behaviour scores were higher during these months than during the rest of the year. Intervals between sexual behaviour peaks for the isolated snow leopardess averaged 3.03 weeks. The sexual behaviour of the paired snow leopards decreased for 8-9 weeks following mating when no offspring were produced, and decreased for 13 weeks in one year when a single cub was born.
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Sulser, C. E., Steck, B. L., & Baur, B. (2008). Effects of construction noise on behaviour of and exhibit use by Snow leopards Uncia uncia at Basel zoo (Vol. 42).
Abstract: Noise caused by human activities can cause stress in animals. We examined whether noise from construction sites affects the behaviour of and exhibit use by three Snow leopards Uncia uncia at Basel zoo. The behaviour and location of the animals were recorded at 1 minute intervals, using the instantaneous scan sampling method over a period of 216 hours (104 hours on noisy days and 112 hours on quiet days). The animals differed individually in their responses to the construction noise. On noisy days, the Snow leopards generally spent less time in locomotion and more time resting, but even on quiet days, resting was the predominant behaviour performed. Under noisy conditions, they increased social resting and decreased resting alone. Walking and social walking were also reduced on noisy days. Furthermore, the Snow leopards spent considerably more time in the remote offexhibit enclosure under noisy conditions. Independent of background noise, they stayed more than half of the time in the caves and the forecourts of the outdoor enclosure. On quiet days, the Snow leopards used more sectors of their exhibit than on noisy days. The results indicate that the Snow leopards responded to construction noise by increasing the amount of time spent resting and by withdrawing to the remote parts of their exhibit.
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Thorel, M. F., Karoui, C., Varnerot, A., Fleury, C., & Vincent, V. (1998). Isolation of Mycobacterium bovis from baboons, leopards and a sea-lion. Vet Res, 29(2), 207–212.
Abstract: This study reports on two series of cases of Mycobacterium bovis infection in zoo animals. The first was in a captive population of baboons (Papio hamadryas) and the second in a mixed group of wild mammals, including four leopards (Panthera uncia and Panthera pardus) and a sea-lion (Otaria byrona). The isolation and identification of strains of M. bovis confirmed the presence of M. bovis infections in both zoos. The epidemiological study using genetic markers such as the IS6110-based DNA fingerprinting system made it possible to differentiate between M. bovis strains. The M. bovis strains isolated from baboons were shown to contain a single IS6110 copy, as usually do cattle isolates, whereas the M. bovis strains isolated from the other exotic animals presented multiple copies. This finding suggests that the origin of the contamination for the baboons in zoo A could be related to cattle. The origin of the contamination for the leopards and sea-lion in zoo B is more difficult to determine. In conclusion, the authors suggest some recommendations for avoiding outbreaks of tuberculosis infections in zoos.
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Turner, L. (1980). Oklahoma City Zoo-Twenty Nine Snow Leopards. Int.Ped Book of Snow Leopards, 2, 96–111.
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Velte, F. (1982). Snow leopards at the Seneca Zoological Park, Rochester. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 55–58). Helsinki: Helsinki Zoo.
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Vogt, P. (1982). New enclosures for snow leopards (Uncia uncia) at Krefeld Zoo. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 67–70). Helsinki: Helsinki Zoo.
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