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Sherpa, L. N., & Lama, W. B. (1997). Hands around Mt. Everest.
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Rana, B. S. (1997). Distinguishing kills of two large mammalian predators in Spiti Valley Himachal Pradesh. J.Bombay Nat.Hist.Soc, 94(3), 553.
Abstract: The author studied livestock killed by predators in the Spiti Valley, India, to determine what species had killed yaks, horses, donkeys, and other domestic animals. Eleven of the kills examined were made by snow leopards and six by the Tibetan wolf. Wolves were involved in surplus killings, while snow leopards kill as food is needed. lgh
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Roth, T. L., Armstrong, D. L., Barrie, M. T., & Wildt, D. E. (1997). Seasonal effects on ovarian responsiveness to exogenous gonadotrophins and successful artificial insemination in the snow leopard (Uncia uncia). Reprod Fertil Dev, 9(3), 285–295.
Abstract: Ovaries of the seasonally-breeding snow leopard (Uncia uncia) were examined to determine whether they were responsive to exogenous gonadotrophins throughout the year. The potential of laparoscopic artificial insemination (AI) also was assessed for producing offspring. During the non-breeding, pre-breeding, breeding and post-breeding seasons, females (n = 20) were treated with a standardized, dual- hormone regimen given intramuscularly (600 I.U. of equine chorionic gonadotrophin followed 80-84 h later with 300 I.U. of human chorionic gonadotrophin (hCG)). Laparoscopy was performed 45-50 h after administration of hCG, and all ovarian structures were described. Females with fresh corpora lutea (CL) were inseminated, and anovulatory females were subjected to follicular aspiration to examine oocyte quality. Snow leopards responded to exogenous gonadotrophins throughout the year. Mean number of total ovarian structures (distinct follicles mature in appearance plus CL) did not differ (P > or = 0.05) with season, but the proportion of CL: total ovarian structures was greater (P < 0.01) for the breeding season compared with all other seasons. The proportion of females ovulating was greater (P < 0.05) during the breeding and post-breeding seasons than during the pre-breeding and non- breeding seasons respectively. No Grade-1 quality oocytes were recovered from follicles of anovulatory females. Serum concentrations of oestradiol-17 beta appeared elevated in all females, and neither oestradiol-17 beta concentrations nor progesterone concentrations differed (P > or = 0.05) among seasons. Of 15 females artificially inseminated, the only one that was inseminated in the non-breeding season became pregnant and delivered a single cub. This is the first successful pregnancy resulting from AI in this endangered species.
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Nowell, K., & Preisser, T. (1997). Saving Their Skins; Pay herders not to hunt snow leopards? Villagers laughed at first.
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Oli, M. K. (1997). Winter home range of snow leopards in Nepal. Mammalia, 61(3), 355–360.
Abstract: Because of their low densities, sparse distribution, elusive behavior, and the precipitous habitat they occupy, snow leopards (Uncia uncia) have been the subject of limited study. This study contributes to that limited database with an investigation of the winter home range of 3 radio-collared snow leopards (2 females and 1 male) in the Annapurna Conservation Area, Nepal. Winter home ranges varied from 13.9-22.3 km2 (x = 19.1). Home ranges overlapped extensively within and between sexes, and an area of 8.1 km2 in the core study site was shared by all three leopards.
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Nowell, K. (1997). Markets for Snow Leopard Products. In R.Jackson, & A.Ahmad (Eds.), (pp. 218–221). Lahore, Pakistan: Islt.
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Norbu, U. P. (1997). Status and Conservation of Snow Leopard In Bhutan. In R.Jackson, & A.Ahmad (Eds.), (pp. 28–34). Lahore, India: International Snow Leopard Trust.
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McCarthy, T., & Munkhtsog, B. (1997). Preliminary Assessment of Snow Leopard Sign Surveys in Mongolia. In R.Jackson, & A.Ahmad (Eds.), (pp. 57–65). Lahore, Pakistan: Islt.
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Lanier, D. L., & Dewsbury, D. A. (1976). A quantitative study of copulatory behaviour of large Felidae. Behavioural-Processes, 1(4), 327–333.
Abstract: Observed a total of 109 copulations in 6 male-female pairs from 4 species of large Felidae. The mean intromission durations were 3.0 sec for Asian leopards (Panthera pardus), 3.3 sec for African leopards (P. pardus), 12.9 sec for snow leopards (Uncia uncia), 2.3 sec for spotted jaguars (P. onca), 3.3 sec for black jaguars (P. onca), and 12.4 sec for Siberian tigers (P. tigris). Behavioral patterns were qualitatively similar across species; all displayed a copulatory pattern with no lock, no intravaginal thrusting, ejaculation on a single insertion, and multiple ejaculations. Whereas domestic cats are reported to assume a neck grip and to tread prior to insertion, these larger Felidae generally did so after intromission had been achieved. After copulation, females of some pairs swiped at the male and displayed a rolling after-reaction. (18 ref) (PsycINFO Database Record (c) 2000 APA, all rights reserved)(unassigned)
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Martin, C. L., Stiles, J., & Willis, M. (1997). Feline colobomatous syndrome. Veterinary-and-Comparative-Ophthalmology, 7(1), 39–43.
Abstract: A syndrome of multiple congenital ocular anomalies in a litter of domestic kittens is described which appears identical to the multiple colobomatous syndrome described in captive Snow Leopards. The lesions varied between kittens in the litter, but ranged from microphthalmos with blindness to mild alterations in the lateral lid margins that resulted in trichiasis. The syndrome of eyelid agenesis in the domestic cat may encompass a broad range of congenital ocular lesions and multiple siblings, but the cause and mechanism of lesion formation is unknown.
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