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Malik, M. M. (1997). The Current Status of Snow Leopards and Their Prey Status and Conservation of Snow Leopard in Pakistan. In R.Jackson, & A.Ashiq (Eds.), (pp. 11–20). Lahore, Pakistan: International Snow Leopard Trust.
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Kitchener, S. L., Meritt, & Rosenthal, M. (1975). Observations on the breeding and husbandry of snow leopards, Panthera uncia. Int.Zoo Yearbook, 15, 212–217.
Abstract: Describes adult care and breeding biology, and the care, growth, and mortality factors of young snow leopards in a successful breeding program in the Lincon Park Zoo, Chicago, Illinois.
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Fox, J. L. (1997). Conflict between predators and people in Ladakh. Cat News, 17, 18.
Abstract: During a six-week period in Hemis National Park, Ladakh, India, snow leopards killed 10 sheep and goats and one leopard gained access to a livestock pen and killed many of the animals inside. Dholes also killed sheep and goats, and a wolf killed a young horse. Residents routinely remove snow leopard cubs from their dens to limit future damage by this species. How to deal with the plight of the people living in the area while still protecting the endangered species are major concerns of the International Snow Leopard Trust, which manages Hemis National Park. lgh.
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Fox, J. L., & Chundawat, R. S. (1997). Evaluation of Snow Leopard Sign Abundance in the Upper Indus Valley. In R.Jackson, & A.Ahmad (Eds.), (pp. 66–74). Lahore, Pakistan: Islt.
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Dhungel, S. (1994). Conservation of the Snow Leopard in Nepal. In J. L. Fox, & D. Jezing (Eds.), (pp. 47–50). Usa: Islt.
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Chundawat, R. S., & Rawat G.S. (1990). Food Habits of Snow Leopard in Ladakh, India.
Abstract: The snow leopard has remained little studied in the past, and most of the information available is either in the form of natural history or anecdotal notes. The inaccessibility of the terrain and its secretive habits make this one of the more difficult animals to study in the wild. In the past decade, several ecological surveys were conducted in India, Nepal, China and Mongolia, which gave us information on the status and distribution of snow leopard (Jackson, Mallon, Fox, Schaller, Chundawat) A detailed study in Nepal through light on its secretive habits ( Jackson and Ahlborn, 1989). Even then little is known about its feeding habits. The present paper discusses this aspect from a study which was part of a detailed study conducted on the ecology of snow leopard in India from October 1987 to Feburary 1990.
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Aramov, B. (1997). The Biology of the Snow Leopard in the Gissarsky Nature Reserve. In R. and A. A. Jackson (Ed.), (pp. 108–109). Lahore, Pakistan: Islt.
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Seidensticker, J., & Lumpkin, S. (1996). The adaptable leopard; unfortunately it's no match for modern man. Wildlife Conservation, 99(3), 52.
Abstract: Abstract: Leopards' adaptability has become the species' vulnerability. The animals do not hesitate to eat rotting flesh and will come back repeatedly to their meal, if disturbed. People have taken advantage of this by lacing carcasses with poison. Leopards are moderate in size compared to other cats, are stealthy and can live in areas as diverse as rain forests and deserts.
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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. M. (1996). Home Range, Movements and Habitat use of Snow Leopard (Uncia uncia) in Nepal. Ph.D. thesis, University of London, University of London.
Abstract: Home ranges for five radio-tagged snow leopards (Uncia uncia) inhabiting prime habitat in Nepal Himalaya varied in size from 11-37 km2. These solitary felids were crepuscular in activity, and although highly mobile, nearly 90% of all consecutive day movements involved a straight line distance of 2km or less. No seasonal difference in daily movement or home range boundry was detected. While home ranges overlapped substancially, use of common core spaces was temporally seperated, with tagged animals being located 1.9 km or more apart during the smae day. Spatial analysis indicated that 47-55% of use occured within only 6-15% of total home area. The snow leopards shared a common core use area, which was located at a major stream confuence in an area where topography, habitat and prey abundance appeared to be more favorable. A young female used her core area least, a female with two cubs to the greatest extent. the core area was marked significantly more with scrapes, Faeces and other sighn than non-core sites, suggesting that social marking plays an important role in spacing individuals. Snow leopards showed a strong preference for bedding in steep, rocky or broken terrain, on or close to a natural vegetation or landform edge. linear landform features, such as a cliff or major ridgeline, were preferred for travelling and day time resting. This behavior would tend to place a snow leopard close to its preferred prey, blue sheep (Psuedois nayaur), which uses the same habitat at night. Marking was concetrated along commonly travelled routes, particularly river bluffs, cliff ledges and well defined ridgelines bordering stream confluences--features that were most abundant within the core area. Such marking may facilitate mutual avoidance, help maintain the species' solitary social structure, and also enable a relatively high density of snow leopard, especially within high-quality habitat.
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