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Marma B.B.and Yunchis V.V. (1968). A contribution to biology of the Snow-leopard (Panthera uncia uncia) (by observations in captivity) (Vol. XLVII, issue 11.).
Abstract: The methods to obtain the progeny of the snow leopard (Panthera uncia uncia) in captivity were being elaborated in the zoological garden of Kaunas, Lithuanian SSR. The blood characteristics for snow leopards is given and compared to that for African lions and Sumatrian tigers. A series of internal, external and clinical indices is established. The rat lasts for 5-7 day, the duration of pregnancy equals 98 days. The duration of lactation varies from 3 to 4 months. Sexual maturity is attained on the 3rd-4th year. From 1960 to 1967 in zoological garden of the world about 29 snow leopards were born, 14 of them in the Kaunas zoological garden.
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Konrath, R. (1975). Snow leopard born at Milwaukee. Animal Keepers' Forum, 11(11).
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Konrath, R. (1975). Snow leopard born at Milwaukee. Animal Keepers' Forum, 11(11).
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Feng, X., Peng, Q., Chen, Y., Li, W. (2022). A Case Study of the Snow Leopard in Sanjiangyuan National Park Boundaries regarding Park Boundary Divergence. Land, 11(813), 1–15.
Abstract: This paper uses remote sensing data from the Sanjiangyuan National Park (SNP) to explore the divergence between the boundaries of national parks and the distribution of natural habitats. Results are used to argue that these discrepancies evolve along with the potential impact of global warming. Using the example of the habitat change of snow leopards and the conflicts between local people and snow leopards, we reflect on the consequences of this divergence. Results show that divergence between the political boundaries and natural habitats as well as the consequent influence on the living conditions of local people are strikingly visible, and the effects of global warming on such conflicts are apparent. The authors conclude that both notions of ‘political boundaries’ and ‘natural habitats’ are expected to come together as the SNP region is spatially configured, while ‘global warming’ seems to be relevant as an essential reference when delimiting the region in the future. Finally, the proposal for the establishment of cooperative conservation areas is presented,
emphasizing the role of cooperative governance in/around national parks.
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Chalise, M. K., & Shakya, P. R. (2002). EDITORIAL: Snow Leopard Investigation in Langtang. Nahson Bulletin, 12-13(2002-2003), 1.
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Lovari, S., Boesi, R., Minder, I., Mucci, N., Randi, E., Dematteis, A., and Ale, S. B. (2009). Restoring a keystone predator may endanger a prey species in a human-altered ecosystem: the return of the snow leopard to Sagarmatha National Park. Animal Conservation, 12, 559–570.
Abstract: Twenty-five years ago, the snow leopard Uncia uncia, an endangered large cat, was eliminated from what is now Sagarmatha National Park (SNP). Heavy hunting pressure depleted that area of most medium-large mammals, before it became a park. After three decades of protection, the cessation of hunting and the recovery of wild ungulate populations, snow leopards have recently returned (four individuals). We have documented the effects of the return of the snow leopard on the population of its main wild prey, the Himalayan tahr Hemitragus jemlahicus, a 'near-threatened' caprin. Signs of snow leopard presence were recorded and scats were collected along a fixed trail (130 km) to assess the presence and food habits of the snow leopard in the Park, from 2004 to 2006. Himalayan tahr, the staple of the diet, had a relative occurrence of 48% in summer and 37% in autumn, compared with the next most frequent prey, musk deer Moschus chrysogaster (summer: 20%; autumn: 15%) and cattle (summer: 15%; autumn: 27%). In early summer, the birth rate of tahr (young-to-female ratio: 0.8-0.9) was high. The decrease of this ratio to 0.1-0.2 in autumn implied that summer predation concentrated on young tahr, eventually altering the population by removing the kid cohort. Small populations of wild Caprinae, for example the Himalayan tahr population in SNP, are sensitive to stochastic predation events and may be led to almost local extinction. If predation on livestock keeps growing, together with the decrease of Himalayan tahr, retaliatory killing of snow leopards by local people may be expected, and the snow leopard could again be at risk of local extinction. Restoration of biodiversity through the return of a large predator has to be monitored carefully, especially in areas affected by humans, where the lack of important environmental components, for example key prey species, may make the return of a predator a challenging event.
Keywords: conservation, food habits, genetics, Hemitragus jemlahicus, Himalayan tahr, management, microsatellite, predation, presence, scat, scat analysis, snow leopard, Uncia uncia
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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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Sharma, K. M. C., Thomas. Johannson, Orjan. Ud Din, Jaffar. Bayarjargal, A. (2010). Snow Leopards and Telemetry: Experiences and Challenges. Telemetry in Wildlife Science, 13(No. 1), 1–5.
Abstract: The snow leopard Panthera uncia is one of the least studied felids in the world. Little is know about various aspects of the ecology of the snow leopard, which is cryptic in nature and found across 12 countries in Central Asia. Most research on snow leopards has been based on non-invasive methods such as sign surveys for presence (e.g. Jackson and Hunter 1996), scat analyses for diet (e.g. Chundawat and Rawat 1992; Oli et al., 2008, 2010) for population estimation, and studies based on human interviews (Mehta and Heinen 2001; Mishra and Bagchi 2006).
Despite this plethora of studies employing non-invasive techniques, several crucial questions about snow leopard ecology remain unanswered. Information about the animal’s home range, dispersal, corridors, pattern of habitat use, movement patterns, hunting frequency, behavior and intra – specific interactions is not available yet. In order to design population monitoring studies using camera traps or DNA analyses, one needs a good understanding of snow leopard ecology, including the home range and movement patterns (Williams et al., 2002). Telemetry is still the best available method and perhaps much less invasive than direct observations for studying the biology and ecology of cryptic animals.
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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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Green, M. J. B. (1987). Protected areas and snow leopards: their distribution and status. Tiger Paper, 14(4), 1–10.
Abstract: Considerable efforts have been devoted to conserving the snow leopard Panthera uncia in recent years, but progress has inevitably been slow due to the difficulties of studying a sparsely distributed, secretive and endangered species in often isolated mountainous terrain. Although knowledge about the species overall distribution in the highlands of Central Asia still remains fragmenatry, it is important to briefly examine all the available information in order to review measures taken to date to conserve the species through the protected areas network. The purpose of this paper is to examine the distribution and status of protected areas inhabited or visited by snow leopard in relation to the species' distribution and highlight deficiences in the present network.
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