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Jackson, R. (1994). Second SLIMS Workshop Held (Vol. xii). Seattle, WA: Islt.
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Oli, M. K. (1996). Seasonal patterns in habitat use of blue sheep Pseudois nayaur (Artiodactyla, Bovidae) in Nepal. Mammalia, 60(2), 187–193.
Abstract: Blue sheep (Pseudois nayaur) are the main prey of the endangered snow leopard (Panthera uncia) as well as an important game species in Nepal. A knowledge of how blue sheep utilize their habitat is essential for the scientific management of the sheep and for the conservation of the snow leopard, but we only have a limited understanding of this aspect of blue sheep ecology. I studied the habitat use pattern of blue sheep by direct observation in the Anna-purna Conservation Area, Nepal where they occur sympatrically with the snow leopard. The sheep used grassland habitats more frequently during pre-parturition (spring) and post-parturition (autumn) than other habitat types, but scrub and grassland habitats were used equally frequently during the rut (winter). The sheep used smooth undulating slopes of medium steepness (<40 degrees) on southerly aspects within the elevation range of 4,200-4,600 m most frequently in all seasons, and there was no evidence of seasonal migration along the elevation gradient. When not in broken landforms (e.g., cliff, landslides), the sheep maintained proximity (less than or equal to 150 m) to such features suggesting their importance as escape cover (i.e., from predators). The use of habitat components by blue sheep appeared to be related to the distribution of foraging areas and escape cover.
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Oli, M. K., & Rogers, E. M. (1996). Seasonal pattern in group size and population composition of blue sheep in Manang, Nepal. Journal of Wildlife Management, 60(4), 797–801.
Abstract: Blue sheep (Pseudois nayaur) are the principal prey of the endangered snow leopard (Panthera uncia) in the Himalayas and adjacent ranges. We studied group size and population composition of blue sheep in Manang District, Annapurna Conservation Area, Nepal. Overall mean group size was 15.6 (SE = 1.3), but it varied seasonally (P lt 0.001), with significantly smaller groups in winter than in other seasons. Mixed groups were most numerous in all seasons, and there was no evidence of sexual segregation. Yearling sex ratio (93.7 M:100 F) did not vary seasonally, nor did the ratio deviate from parity. Adult sex ratio showed a seasonal pattern favoring males post-parturition but female-biased during the rut and pre-parturition. Seasonal variation in sex-specific mortality is offered as a plausible explanation for the observed pattern in adult sex ratio.
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Johnston, L. A., Armstrong, D. L., & Brown, J. L. (1994). Seasonal effects on seminal and endocrine traits in the captive snow leopard (Panthera uncia). J Reprod Fertil, 102(1), 229–236.
Abstract: The annual reproductive cycle of the male snow leopard (Panthera uncia) was characterized by evaluating seminal and endocrine traits monthly. Testicular volume was greatest (P < 0.05) during the winter months when the quality of ejaculate was optimal. Ejaculate volume, total sperm concentration ml-1, motile sperm concentration per ejaculate, sperm morphology and sperm motility index were lowest during the summer and autumn months compared with the winter and spring. Peripheral LH, FSH and testosterone concentrations were also lowest during the summer months, increasing during the autumn just before the increase in semen quality, and were maximal during the winter months. There was a direct relationship (P < 0.01) between: (1) testosterone and testicular volume, total sperm concentration ml-1, motile sperm concentration per ejaculate and ejaculate volume, and (2) LH and testicular volume and motile sperm concentration per ejaculate. In summary, although spermatozoa were recovered throughout the year, optimal gamete quality was observed during the winter and spring. Although previous studies in felids have demonstrated seasonal effects on either seminal or endocrine traits, this is the first study to demonstrate a distinct effect of season on both pituitary and testicular function.
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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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Hunter, D. O. (1991). Science and Spirit:GIS tracks the elusive snow leopard. GeoInfo Systems, Jan, 21–28.
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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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Schaller, G. (1990). Saving China's Wildlife. International Wildlife, 1(2), 30–41.
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Anonymous. (2000). Save the Snow Leopard. (Road and Gas Pipeline Project Threatens Ecology of Siberia). The Ecologist, 30(4), 14.
Abstract: An interregional organisation called Siberian Accord plans to construct a road and gas pipeline to China, This association, which has vast political powers, exists to create favorable conditions for investing in Siberia.
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Mainka, S. A. (1988). Revision of a Total Hip Replacement in a Snow Leopard. In H.Freeman (Ed.),. Usa: ISLT and Wildlife Institute of India.
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