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Lutz, H., Isenbugel, E., & Lehmann, R. (1994). Retrovirus serology in snow leopards and other wild felids in European zoos. In J.L.Fox, & D.Jizeng (Eds.), (pp. 203–208). Usa: Islt.
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Anonymous. (1994). Resolutions Conservation of Snow Leopard, Seventh International Snow Leopard Symposium. In J.L.Fox, & D.Jizeng (Eds.), (pp. 329–331). Usa: Islt.
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Freeman, H. (1988). Resolutions Conservation of Snow Leopard, Fifth International Snow Leopard Symposium. (pp. 267–269). Usa.
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Johnson, W. E., Dratch, P. A., Martenson, J. S., & O'Brien, S. J. (1996). Resolution of recent radiations within three evolutionary lineages of Felidae using mitochondrial restriction fragment length polymorphism variation. Journal of Mammalian Evolution, 3(2), 97–120.
Abstract: Patterns of mitochondrial restriction fragment length polymorphism (RFLP) variation were used to resolve more recent relationships among the species of the Felidae ocelot lineage, domestic cat lineage, and pantherine lineage. Twenty-five of 28 restriction enzymes revealed site variation in at least 1 of 21 cat species. The ocelot lineage was resolved into three separate sister taxa groups: Geoffroy's cat (Oncifelis geoffroyi) and kodkod (O. guigna), ocelot (Leopardus pardalis) and margay (L. wiedii), and pampas cat (Lynchailurus colocolo) and most of the tigrina samples (Leopardus tigrina). Within the domestic cat lineage, domestic cat (Felis catus), European wild cat (F. silvestris), and African wild cat (F. libyca) formed a monophyletic trichotomy, which was joined with sand cat (F. margarita) to a common ancestor. Jungle cat (F. chaus) and black-footed cat (F. nigripes) mtDNAs diverged earlier than those of the other domestic cat lineage species and are less closely related. Within the pantherine lineage, phylogenetic analysis identified two distinct groups, uniting lion (P. leo) with leopard (P. pardus) and tiger (P. tigris) with snow leopard (P. uncia).
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Johnston, L. A., Donoghue, A. M., O'Brien, S. J., & Wildt, D. E. (1991). Rescue and maturation in vitro of follicular oocytes collected from nondomestic felid species. Biol Reprod, 45(6), 898–906.
Abstract: The potential for rescuing immature oocytes from the ovaries of females of rare felid species which die or undergo medical ovariohysterectomy was evaluated. Ovaries were recovered from 13 species representing 35 individuals in good-to-poor health. Although the majority of females were 10 yr of age or older and in fair-to-poor health, a total of 846 oocytes were recovered of which 608 (71.9%) were classified as fair-to- excellent quality. One hundred of these oocytes were used for initial maturation classification and as parthogenetic controls. Overall, of the 508 fair-to-excellent quality oocytes placed in culture, 164 (32.3%) matured to metaphase II in vitro. For species in which 3 or more individuals yielded oocytes, mean oocyte maturation rates were as follows: 36.2%, tiger; 27.9% leopard; and 8.3%, cheetah. In vitro insemination of oocytes resulted in fertilization (2 polar bodies, 2 pronuclei, or cleavage) rates of 9.1% to 28.6% (leopard) using homologous fresh spermatozoa and 4.0% (lion) to 40.0% (puma) using homologous frozen-thawed spermatozoa. Inseminations using heterologous (domestic cat) spermatozoa also resulted in fertilized oocytes in the tiger, leopard, snow leopard, puma, serval, and Geoffroy's cat (range in fertilization rate, 5.0% for leopard to 46.2% for puma). Cleaved embryos resulted from the insemination of leopard oocytes with homologous sperm (n = 1 embryo) and puma oocytes with domestic cat sperm (n = 3 embryos). These results demonstrate that immature ovarian oocytes from rare felid species can be stimulated to mature in vitro despite an excision-to-culture interval as long as 36 h.(ABSTRACT TRUNCATED AT 250 WORDS)
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Bold, A., & Dorzhzunduy, S. (1976). Report on Snow Leopards in the Southern Spurs of the Gobi Altai. (Vol. 11, pp. 27–43).
Abstract: Estimates a population of 170-230 snow leopard within an area of 6600 km2 in Southern Gobi
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Bajimaya, S., Baral N., & Yadav L.B. (1990). Report on Overall Assessment of Dhorpatan Hunting Reserve.
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Jackson, R., & Fox, J. L. (2000). Report on Fifth Slims Training Workshop (Nepal) (Vol. xvii). Seattle: International Snow Leopard Trust.
Abstract: Nepal's snow leopards (Uncia uncia) are mostly found along the northern border with Tibet (China). The largest populations are in Dolpa, Mugu, Manang, and Myagdi Districts. Potential habitat totals about 30,000 square kilometers. Numbers are estimated at 300-500, but surveys are urgently needed to confirm this rough guess. Like elsewhere, the primary threats center on poaching, depletion of natural prey, livestock depredation and resultant retributive killing of snow leopards by herders, and the lack of public awareness and support for conserving snow leoaprds, especially among local herders.
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Prasad, S. N., Chundawat, R. S., Hunter, D. O., Panwar, H. S., & Rawat, G. S. (1991). Remote sensing snow leopard habitat in the trans-Himalaya of India using spatial models and satellite imagery preliminary results. In G. J. Buhyoff (Ed.), (pp. 519–523).
Abstract: The snow leopard (Panthera uncia) is a flagship species for conservation in the high mountain regions of central Asia. Data on snow leopard predation, habitat conditions and range of main prey species were gathered along with thematic maps of the study area for elevation, snow cover, sighting data, kill data, blue sheep use areas, and vegetation data. These data were entered into a GIS and used to help delineate surface features from a satellite image. Preliminary results show that general physiographic features of snow leopard habitat can be detected using satellite imagery and that GIS cartographic modeling techniques can improve this delineation. -from Authors
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Kreuzberg-Mukhina, E., Bikova, E., & Esipov, A. Regional Meeting on the Protection of Snow Leopard.
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