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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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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Rowell, G. (1983). China's Wildlife Lament. International Wildlife, 13(6), 4–11.
Abstract: Reports sightings of snow leopard in Qinghai Province. One freshly killed; a 15 yuan bounty exists on snow leopards
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Saberwal, V. K. (1996). Pastoral Politics:gaddi grazing, degradation and biodiversity conservation in Himachal Pradesh, India. Conservation Biology, 10, 741–749.
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Salles, L. O. (1992). Felid phylogenetics: Extant taxa and skull morphology (Felidae, Aeluroidae). American Museum Novitates, (3047), 1–67.
Abstract: relationships among extant felid taxa are controversial. A historical appraisal addresses component congruence among statements on felid phylogenetic relationships, and monophyly of generic ranks proposed for felids is discussed. Felid cranial morphology (especially the masticatory apparatus, basicranium, and rostral regions) is examined, and 44 characters are postulated for 39 taxa. Internal congruence for these characters is evaluated and 27 components are suggested. Parsimony analysis, using the successive weighting option of Hennig86, of the 44 cranial characters plus 13 other morphological features yields 29 components in a “modified Nelson” consensus cladogram. Two basal, well resolved clades are hypothesized in the total morphology analysis; under parenthetical notation the first is: (Hepailurus yagouaroundi (Puma concolor (Acinonyx jubatus (Uncia uncia (Neofelis nebulosa (Panthera tigris (P. onca, P. leo, and P. pardus)))))). The second clade is: Profelis temmincki (P. badia (Pardofelis marmorata ((Caracal caracal (Lynx rufus (L. lynx (L. pardina (L. canadensis)))) (Felis chaus (F. lybica (L. cafra (L. silvestris (F. bieti (F. nigripes (F. margarita (Octocolobus manul)))))))). Prionailurus planiceps and P. viverrina formed another group which is suggested as the basal branch of the felid phylogeny. The results in this study do not support monophyly of Leopardus Gray, 1841; Profelis Severtzon, 1858; and Prionailurus Severtzon, 1858. A better supported, more highly resolved, felid phylogenetic tree is needed.
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Samant S.S., Dhar U., & Rawal R.S. (1998). Biodiversity status of a protected area in West Himalaya: Askot Wildlife Sanctuary. International Journal Of Sustainable Development And World Ecology, 5(3), 194–203.
Abstract: Biodiversity of a protected area of West Himalaya (Askot Wildlife Sanctuary) was studied and analysed for landscape, faunal and floral diversity. The forest and pasture land, ideal habitats for the flora and fauna, covered nearly 52% and 12%, respectively, of total reported area. Among the fauna Himalayan musk deer (Moschus chrysogaster), thar (Himitragus jemlahicus), snow leopard (Panthera uncia), koklas (Pucrassia macrolophas), monal (Lophophorus impejanus) and snow cock (Tetragalus tibetanus) are threatened species. Plant diversity is represented by 1262 species of vascular plants (Angiosperm 1112, Gymnosperm 7, Pteridophytes 143 taxa). Diversity of the species within families, genera, habitats, communities and along vertical gradient zone was analysed. Maximum diversity existed in the family Orchidaceae (120 taxa), genera Polystichum (13 taxa), altitude zone (1001-2000 m; 860 taxa), habitat (forest; 623 taxa) and community (Banj oak: 92 taxa). Seventy-one families were found to be monotypic. Species were further analysed for ethnobotanical use (medicine: 70, edible: 55, fodder: 115, fuel: 31, house building: 13 etc.), domesticated diversity (crops: 19, vegetables: 26, fruits: 16),agroforestry or marginal, threatened and endemic diversity. Similarity in species composition within the habitats indicated maximum similarity in areas of shrubberies and alpine meadows/slopes (71.65%) and exposed open/grassy slopes and shady moist places (47.32%). 432 (34.2%) taxa are native to Indian Himalaya of which 24 are endemic and 235 are near endemics. 65.8% of taxa are represented in the neighbouring areas and other regions of the globe. Ten taxa occurring in the Sanctuary have been already recorded in the Red Data Book of Indian Plants. Conservation and management of species is focused.
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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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Sayer, J. A. (1980). The conservation of the snow leopard (Uncia uncia) in Afghanistan. International Pedigree Book of Snow Leopards, 2, 55–61.
Abstract: Outlines status and distribution as well as recent sightings of snow leopard in Afganastan
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Schaffer, E., Wiesner, H., & Von Hegel, G. (1988). Multiple ocular coloboma (MOC) with persistent pupillary membrane in the snow leopard (Panthera uncia). Tierarztl Prax, 16(1), 87–91.
Abstract: In a litter of three snow leopards, bilateral colobomata of the upper temporal eyelids, bilateral persistent pupillary membranes and a unilateral coloboma of the optic nerve entrance are described as “Multiple Ocular Colobomata” (MOC). The causal pathogenesis of each of the colobomata is discussed comparatively. The colobomata of the eyelids, essential feature of the MOC syndrome in snow leopards, are most probably not of hereditary, but rather of intrauterine infectious viral origin.
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Schaller, G. B. (1972). On the behaviour of Blue Sheep (Pseudois nayaur). Journal of Bombay Natural Historical Society, 69, 523–537.
Abstract: Two or three snow leopards hunted in the study area in eastern Nepal. Describes content of some snow leopard scat
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