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Blomqvist, L. (1995). The snow leopard in captivity in 1992. International Zoo News, 42(3), 152–159.
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Calle, P. P., Colter, S. B., Taylor, R. A., & Wright, A. M. (1989). Extramedullary thoracolumbar fungal (scopulariopsis-brumptii) abscesses in 2 snow leopard (Panthera-uncia) littermates. Journal of Zoo and Wildlife Medicine, 20(3), 346–353.
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Chakraborty, R. E., & Chakraborty, S. (1996). Identification of dorsal guard hairs of Indian species of the genus Panthera Oken (Carnivora: Felidae). Mammalia, 60(3), 480.
Abstract: Dorsal guard hairs of four living Indian species of the genus Panthera, viz. P. tigris, P. leo, P. pardus and P. uncia have been studied. It is found that the characters are somewhat overlapping, but identification of the species may be possible from the combination of characters.
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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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Fox, J. L., Sinha, S. P., Chundawat, R. S., & Das, P. K. (1991). Status of the snow leopard Panthera uncia in Northwest India. Biological Conservation, 55(3), 283–298.
Abstract: Evidence of snow leopard presence was most abundant in C Ladakh, decreased southward toward the crest of the Himalaya, and was least on the S side of the main Himalaya. Prey populations, primarily blue sheep Pseudois nayaur and Asiatic ibex Capra ibex, were also more plentiful in the areas surveyed to the N of the main Himalaya. Perhaps 400 snow leopard occur throughout NW India. The stronghold of this species in India is apparently the trans- Himalayan ranges in Ladakh where new parks and reserves are being established, some in association with a snow leopard recovery programme of the state of Jammu and Kashmir and a 'Project Snow Leopard' of the central Indian government. Because of the generally low density of snow leopard, conservation measures must also be considered within the large areas of its range lying outside parks and reserves. -from Authors
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Graham, L. H., Goodrowe, K. L., Raeside, J. I., & Liptrap, R. M. (1995). Non-invasive monitoring of ovarian function in several felid species by measurement of fecal estradiol-17-beta and progestins. Zoo Biology, 14(3), 223–237.
Abstract: An extraction and assay procedure to measure fecal estradiol-17-beta and progestin concentrations in several cat species was developed and validated for use for noninvasive monitoring of ovarian function. Fecal samples were collected over a range of 3-20 months from female tigers (three), lions (three), snow leopards (three), cheetahs (two), caracals (two), and domestic cats (five). Samples were extracted with 90% methanol, lipids removed with petroleum ether, and the estradiol and progestins in the methanol measured by radioimmunoassay (RIA). High Performance Liquid Chromatography (HPLC) fractionation and subsequent RIA of the fractions indicated that the estradiol-17-beta antiserum cross-reacted primarily with estradiol-17-beta in the feces of lions and tigers and was assumed to be specific for estradiol-17-beta in the feces of other species as well. However, there were several immunoreactive compounds, presumably progesterone metabolites, excreted in the feces which varied both quantitatively and qualitatively among species. The behavior of tigers, lions, cheetahs, and caracals was visually monitored during the collection period and frequency of sexual behaviors was positively correlated with increases in fecal estradiol in all species observed. The mean fecal estradiol-17-beta peaks were as follows: tigers, 128.0 +- 13.1; lions, 186.0 +- 14.8; snow leopards, 136.7 +- 15.9; cheetahs, 140.9 +- 9.0; caracals, 24.5 +- 4.0; and domestic cats 158.9 +- 19.3 ng/gm. Fecal progestin concentrations rose significantly (P lt 0,001) only after breeding or during pregnancy and were as follows: tigers, 5.6 +- 0.6; lions, 1.9 +- 0.1; cheetahs, 8.4 +- 1.1; and caracals, 2.4 +- 0.4 mu-g/gm. Fecal progestins were elevated for one-half to two-thirds of the gestation length during presumed pseudopregnancy but remained elevated throughout successful pregnancies. These results suggest that ovarian function can be monitored noninvasively in the family Felidae by the measurement of fecal estradiol-17-beta and progestin concentrations.
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Jackson, R., & Ahlborn, G. (1989). Catching a ghost (the snow leopard). International Wildlife., 19(3), 30.
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Jackson, R., Roe, J., Wangchuk, R., & Hunter, D. (2006). Estimating Snow Leopard Population Abundance Using Photography and Capture-Recapture Techniques (Vol. 34).
Abstract: Conservation and management of snow leopards (Uncia uncial) has largely relied on anecdotal evidence and presence-absence data due to their cryptic nature and the difficult terrain they inhabit. These methods generally lack the scientific rigor necessary to accurately estimate population size and monitor trends. We evaluated the use of photography in capture-mark-recapture (CMR) techniques for estimating snow leopard population abundance and density within Hemis National Park, Ladakh, India. We placed infrared camera traps along actively used travel paths, scent-sprayed rocks, and scrape sites within 16-30 kmý sampling grids in successive winters during January and March 2003-2004. We used head-on, oblique, and side-view camera configurations to obtain snow leopard photographs at varying body orientations. We calculated snow leopard abundance estimates using the program CAPTURE. We obtained a total of 66 and 49 snow leopard captures resulting in 8.91 and 5.63 individuals per 100 trap nights during 2003 and 2004, respectively. We identified snow leopards based on the distinct pelage patters located primarily on the forelimbs, flanks, and dorsal surface of the tail. Capture probabilities ranged from 0.33 to 0.67. Density estimates ranged from 8.49 (SE+0.22) individuals per 100 kmý in 2003 to 4.45 (SE+0.16) in 2004. We believe the density disparity between years is attributable to different trap density and placement rather than to an actual decline in population size. Our results suggest that photographic capture-mark-recapture sampling may be a useful tool for monitoring demographic patterns. However, we believe a larger sample size would be necessary for generating a statistically robust estimate of population density and abundance based on CMR models.
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Jalanka, H. H., & Roeken, B. (1990). The use of Medetomidine, Medetomidine-Ketamine combinations, and Atipamezole in nondomestic mammals: A review. Journal-of-Zoo-and-Wildlife-Medicine, 21(3), 259–282.
Abstract: The recent development of potent and specifica lphar-adrenoceptoar gonistsa nd antagonists has enhanced their use in nondomestic animal immobilization and reversal. Medetomidine, a new potent alphar-agonist, in combination with the dissociative anesthetic ketamine, has been used to immobilize a variety of nondomestic mammals. Medetomidine alone induces sedation in a dose-dependent way, and complete immobilization has been achieved with high doses in semidomesticated reindeer (Rangifer tarandus) and blue foxes (Alopex lagopus). Howbver, we feel that ketamine should be added to the immobilization mixture to ensure complete immobilization and operator safety. In ketamine combinations, medetomidine doses are usually 60-100 pg/kg. The required ketamine doses are remarkably low:0.8-1.6 mglkg in most ruminants,2.5-3.0 mgUgin felids,u rsids,a nd canids,a nd 5.G-8.0m glkgi n primates,w olverines(Gulog ulo),ando therm uitelids. Clinically, the resulting immobilization is characterized by a smooth onset, good to excellent myorelaxation, and areflexia at higher doses. Determinations of hematologic, serum biochemicil, arterial blood gas,a nd acid-bases tatusp arametersi ndicate that the immobilization is physiologically sound. We have had no fatalities attributable to the immobilization mixture ( I ,240 immobilizations). The alphar-adrenoceptora ntagonist,a tipamezole,i s highly efective in reversingt he immobilization induced by medetomidine, medetomidine-ketamine combinations, or xylazine. In ruminants, the medetomidine-ketamine-induced immobilization can be rapidly and persistently reversed by administering 100-l 50 1rg/kg of alipamezole i.v. and the rest s.c., adjusting the total atipamezole dose to an atipamezole: medetomidine ratio of approximately 4-5 (w/w). Becauseth e required ketamine doses are relatively high in carnivores, we prefer to use a lower atipamezole dose (totil atipamezoie: medetomidine ratio approximately 2-3 w/w) and to administer it i.m. or s.c. Using thii regimen, reversals are calm and animals show minimal “residual ketamine effect.” Because atipamezole is a competitive antagonist, its dose should be reduced if it is administered late in the immobilization period when a large part of medetomidine has been endogenously metabolized. Xylazine-induced immobilization is rapidly reversed by I mg of atipamezole for every 8-12 mg of xylazine used.
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Karesh, W. B., & Asterino, R. (1988). Mandibular osteomyelitis in a snow leopard (Panthera-uncia) with a review of osteomyelitis in other species and man. Journal Of Zoo Animal Medicine, 19(3), 137–142.
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