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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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Wemmer, C., & Sunquist, M. (1988). Felid Reintroductions: Economic and Energetic Considerations. In H.Freeman (Ed.), (pp. 193–205). India: International Snow Leopard Trust and Wildlife Institute of India.
Abstract: Reintroduction and captive breeding are often touted as panaceas for extinction in the wild. The populace at large, educated insuch matters by the mass media, places great faith in such wildlife technology. Furthermore, the wildlife professionals who develope recovery and managemnt plans for endangered species often include a section on reintroduction and sometimes advocate captive breeding as a source of colonizing stock.
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Kuznetzov B.A. (1948). Felidae (Vol. Vol.13 (XXVIII)).
Abstract: The snow leopard widely wide distributed in mountains of Middle and Central Asia. Irbis meets in Altai, Saur, Tarbagatai, Jungarian and Zaili Ala Tau, Kirghiz ridge and Talass within the Kazakhstan. The snow leopard is very rare in Southern Altai, and probably it stay here occasionally.
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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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Fix, A. S., Riordan, D. P., Hill, H. T., Gill, M. A., & Evans, M. B. (1989). Feline panleukopena virus and subsequent canine-distemper virus infection in two snow leopards (Panthera uncia). Journal of Zoo and Wildlife Medicine, 20(3), 273–281.
Abstract: Two adult snow leopards (Panthera uncia), male and female, both with vaccinations current, became infected with feline panleukopenia virus (FPV) at the Blank Park Zoo, Des Moines, Iowa, in late 1988. Clinical signs included weakness, hemorrhagic feces, fever, seizures, and nasal discharge. Blood analysis revealed severe lymphopenia and mild anemia. A positive enzyme-linked immunosorbent assay (ELISA) test for FPV on fecal contents from the male leopard confirmed the diagnosis. In spite of intensive therapy, both animals died. Necropsy of the female, which survived for 1 wk after onset of signs, revealed intestinal crypt necrosis, pulmonary consolidation, necrotizing laryngitis, and diffuse lymphoid depletion. The male leopard, which lived 3 wk after onset of illness, had similar enteric and lymphoid lesions. In addition, there was a severe interstitial pneumonia, with syncytial cells containing eosinophilic intracytoplasmic inclusion bodies. Ultrastructural characteristics of these inclusions featured tubular structures consistent with a paramyxovirus. Although repeated virus isolation attempts from the affected lung were negative, polyclonal and monoclonal fluorescent antibody tests were strongly positive for canine distemper virus (CDV). Frozen paired sera from each leopard demonstrated very high acute and convalescing titers to FPV; both animals also seroconverted to CDV, with titers in the male leopard higher than those in the female. Additional tests for toxoplasmosis, feline infectious peritonitis, feline rhinotracheitis, feline calicivirus, feline leukemia, canine parainfluenza, and bovine respiratory syncytial virus were all negative. The neurologic signs present in these leopards remained unexplained, but may have been attributable to CDV infection. A feral cat trapped on zoo property had feces positive for FPV by ELISA. Although the specific contributions of FPV and CDV toward the development of this case are unknown, it is likely that initial FPV-induced immunosuppression allowed the subsequent development of CDV in these snow leopards. The likelihood that initial FPV infection came from feral cats underscores the importance of feral animal control on zoo premises.
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Sundberg, J. P., Van Ranst, M., Montali, R., Homer, B. L., Miller, W. H., Rowland, P. H., et al. (2000). Feline papillomas and papillomaviruses. Vet Pathol, 37(1), 1–10.
Abstract: Papillomaviruses (PVs) are highly species- and site-specific pathogens of stratified squamous epithelium. Although PV infections in the various Felidae are rarely reported, we identified productive infections in six cat species. PV-induced proliferative skin or mucous membrane lesions were confirmed by immunohistochemical screening for papillomavirus-specific capsid antigens. Seven monoclonal antibodies, each of which reacts with an immunodominant antigenic determinant of the bovine papillomavirus L1 gene product, revealed that feline PV capsid epitopes were conserved to various degrees. This battery of monoclonal antibodies established differential expression patterns among cutaneous and oral PVs of snow leopards and domestic cats, suggesting that they represent distinct viruses. Clinically, the lesions in all species and anatomic sites were locally extensive and frequently multiple. Histologically, the areas of epidermal hyperplasia were flat with a similarity to benign tumors induced by cutaneotropic, carcinogenic PVs in immunosuppressed human patients. Limited restriction endonuclease analyses of viral genomic DNA confirmed the variability among three viral genomes recovered from available frozen tissue. Because most previous PV isolates have been species specific, these studies suggest that at least eight different cat papillomaviruses infect the oral cavity (tentative designations: Asian lion, Panthera leo, P1PV; snow leopard, Panthera uncia, PuPV-1; bobcat, Felis rufus, FrPV; Florida panther, Felis concolor, FcPV; clouded leopard, Neofelis nebulosa, NnPV; and domestic cat, Felis domesticus, FdPV-2) or skin (domestic cat, F. domesticus, FdPV-1; and snow leopard, P. uncia, PuPV-2).
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Gromov I.M. (1963). Felis (Uncia) uncia Schreber (1776) leopard or irbis (Vol. Part.2.).
Abstract: An identification table for genus and species of mammals of USSR is given. The taxonomy, morphology, distribution and life history are described. The features of snow leopard Felis (Uncia) uncia, distribution, biology and practical value are described.
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Karmacharya, D. (2011). Field Protocol – Scat Collection for Genetic Analysis.
Abstract: Project funded by Snow Leopard Conservation Grant Program. Center for Molecular Genetics, Nepal.
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Hillard, D. (1986). Field report form the Himala V an Snow Leopard Project: Survey In Hongu Valley After participating in the Fifth International Snow Leopard Symposium in Srinagar.1–3.
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Aryal, A. (2009). Final Report On Demography and Causes of Mortality of Blue Sheep (Pseudois nayaur) in Dhorpatan Hunting Reserve in Nepal.
Abstract: A total of 206 individual Blue sheep Pseudois nayaur were estimated in Barse and Phagune blocks of Dhorpatan Hunting Reserve (DHR) and population density was 1.8 Blue sheep/sq.km. There was not significant change in population density from last 4 decades. An average 7 animals/herd (SD-5.5) were classified from twenty nine herds, sheep per herds varying from 1 to 37. Blue sheep has classified into sex ratio on an average 75 male/100females was recorded in study area. The sex ratio was slightly lower but not significantly different from the previous study. Population of Blue sheep was seen stable or not decrease even there was high poaching pressure, the reason may be reducing the number of predators by poison and poaching which has
supported to increase blue sheep population. Because of reducing the predators Wolf Canis lupus, Wild boar population was increasing drastically in high rate and we can observed wild boar above the tree line of DHR. The frequency of occurrence of different prey species in scats of different predators shows that, excluding zero values, the frequencies of different prey species were no significantly different (ö2= 10.3, df = 49, p > 0.05). Most of the scats samples (74%) of Snow leopard, Wolf, Common Leopard, Red fox's cover one prey species while two and three species were present in 18% and 8%, respectively. Barking deer Muntiacus muntjak was the most frequent (18%) of total diet composition of common leopards. Pika Ochotona roylei was the most frequent (28%), and Blue sheep was in second position for diet of snow leopards which cover 21% of total diet composition. 13% of diet covered non-food item such as soil, stones, and vegetable. Pika was most frequent on Wolf and Red fox diet which covered 32% and 30% respectively. There was good positive relationship between the scat density and Blue sheep consumption rate, increasing the scat density, increasing the Blue sheep consumption rate. Blue sheep preference by different predators such as Snow leopard, Common leopard, Wolf and Red fox were 20%, 6%, 13% and 2% of total prey species respectively.
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