Kinsel, M. J., Kovarik, P., & Murnane, R. D. (1998). Gastric spiral bacteria in small felids. Journal-of-Zoo-and-Wildlife-Medicine, 29(2), 214–220.
Abstract: Nine small cats, including one bobcat (Felis rufus), one Pallas cat (F. manul), one Canada lynx (F. lynx canadensis), two fishing cats (F. viverrina), two margays (F. wiedii), and two sand cats (F. margarita), necropsied between June 1995 and March 1997 had large numbers of gastric spiral bacteria, whereas five large cats, including one African lion (Panthera leo), two snow leopards (P. uncia), one Siberian tiger (P. tigris altaica), and one jaguar (P. onca), necropsied during the same period had none. All of the spiral organisms from the nine small cats were histologically and ultrastructurally similar. Histologically, the spiral bacteria were 5-14 mum long with five to nine coils per organism and were located both extracellularly within gastric glands and surface mucus, and intracellularly in parietal cells. Spiral bacteria in gastric mucosal scrapings from the Canada lynx, one fishing cat, and the two sand cats were gram negative and had corkscrew-like to tumbling motility when viewed with phase contrast microscopy. The bacteria were 0.5-0.7 mum wide, with a periodicity of 0.65-1.1 mum in all cats. Bipolar sheathed flagella were occasionally observed, and no periplasmic fibrils were seen. The bacteria were extracellular in parietal cell canaliculi and intracellular within parietal cells. Culture of mucosal scrapings from the Canada lynx and sand cats was unsuccessful. Based on morphology, motility, and cellular tropism, the bacteria were probably Helicobacter-like organisms. Although the two margays had moderate lymphoplasmacytic gastritis, the other cats lacked or had only mild gastric lymphoid infiltrates, suggesting that these organisms are either commensals or opportunistic pathogens.
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O'Gara, B. W. (1988). Snow leopards and sport hunting in the Mongolian People's Republic. (pp. 215–225). India: International Snow Leopard Trust and The Wildlife Institute of India.
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Freeman, H. (1974). A preliminary study of the behaviour of captive snow leopards (Panthera uncia). In International Zoo Yearbook (Vol. 15, pp. 217–222).
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Blomqvist, L. (1980). The snow leopard register. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 218–238). Helsinki: Helsinki Zoo.
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Esipov A.V. (2003). Snow Leopard (Irbis) (Vol. Vol. II. Animals.).
Abstract: Critically Endangered l (CR C2a(i); D), locally distributed western subspecies of Central Asian species. It occurs in Western Tien Shan and Western Pamir Alay. It inhabits middle and high belts of the mountains. It prefers watersheds and rocky talus slopes. It never was numerous; last decades the numbers have been decreasing. In 1980's-1990's in Hissar nature reserve 5-11 individuals were counted, in 1970's-1980's in Chatkal nature reserve the 1-3 specimens were observed. Perhaps, total number is 20-30 individuals. The threats are development of high mountain pastures, decreasing of prey numbers, human persecution and poaching. Included in the IUCN Red List [EN] and in Appendix I of CITES.
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Medvedev D.G. (2003). Distribution and migration of the snow leopard in Baikal region.
Abstract: It provided description of snow leopard distribution in Eastern Sayan, South Transbaikalia and mountains of Baikal lake as well as its migratory ways within the region.
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Xu, F., Ming, M., Yin, S. -jing, & Munkhtsog, B. (2006). Autumn Habitat Selection by Snow Leopard (Uncia uncia) in Beita Mountain, Xinjiang, China.
Abstract: Habitat selection of Snow Leopard ( Unica unica) in Beita Mountain of the Altay Mountain system in northeast Xinjiang was conducted from September to October 2004. Six habitat features of 59 sites used by Snow Leopard and 30 random plots were measured by locating 15 transects surveys in the study area . Vanderploge and Scaviaps selectivity index was used to assess Snow Leopardps selection for the different habitat parameters. Principal Component Analysis was used as the primary factor . The results indicated that Snow Leopard preferred the altitude between 2000 – 2 200 m and avoided 2 600 – 3 000 m ; selected cliff base , ridgeline and avoided hillside and valley bottom ; utilized the shrub and rejected the forest ; selected the nongrazing area and avoided the slightly broken region ; preferred north orientation and rejected the south orientation. The results show that grazing status , vegetation type , topography and the ruggedness are the primary factors for the habitat selection of Snow Leopard.
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Bannikov A.G. (1966). Mountains of Middle Asia and Kazakhstan.
Abstract: The data on geographical location, plants and animals of mountain nature reserves of Middle Asia and Kazakhstan are given. Snow leopard and its preys (wild ibexes and sheep) were recorded in both Almaty and Aksu Jabagly nature reserves.
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Sludsky A.A. (1982). Genus Snow leopard Uncia Gray, 1854. Snow leopard Uncia uncia Schreber, 1775 (Vol. Vol. III, Part 2.).
Abstract: Snow leopard is rare and extinctive species that have scientific and aesthetic significance. The features of genus Uncia and species Uncia uncia are described. Also distribution, habitat, way of life, reproduction biology, behavioural patterns, migration routes, infections and parasites, enemies and competitors, number and number fluctuation, practical value of snow leopard in the Kazakhstan are given.
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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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