Jackson, R., Roe, J., Wangchuk, R., & Hunter, D. (2005). Camera-Trapping of Snow Leopards. Cat News, 42(Spring), 19–21.
Abstract: Solitary felids like tigers and snow leopards are notoriously difficult to enumerate, and indirect techniques like pugmark surveys often produce ambiguous information that is difficult to interpret because many factors influence marking behavior and frequency (Ahlborn & Jackson 1988). Considering the snow leopard's rugged habitat, it is not surprising then that information on its current status and occupied range is very limited. We adapted the camera-trapping techniques pioneered by Ullas Karanth and his associates for counting Bengal tigers to the census taking of snow leopards in the Rumbak watershed of the India's Hemis High Altitude National Park (HNP), located in Ladakh near Leh (76ø 50' to 77ø 45' East; 33ø 15' to 34ø 20'North).
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McCarthy, T., Khan, J., Ud-Din, J., & McCarthy, K. (2007). First study of snow leopards using GPS-satellite collars underway in Pakistan. Cat News, 46(Spring), 22–23.
Abstract: Snow leopards (Uncia uncia) are highly cryptic and occupy remote inaccessible habitat, making studying the cats difficult in the extreme. Yet sound knowledge of the cat's ecology, behavior and habitat needs is required to intelligently conserve them. This information is lacking for snow leopards, and until recently so was the means to fill that knowledge gap. Two long-term studies of snow leopards using VHF radio collars have been undertaken in Nepal (1980s) and Mongolia (1990s) but logistical and technological constraints made the findings of both studies equivocal. Technological advances in the interim, such as GPS collars which report data via satellite, make studies of snow leopards more promising, at least in theory.
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Lanier, D. L., & Dewsbury, D. A. (1976). A quantitative study of copulatory behaviour of large Felidae. Behavioural-Processes, 1(4), 327–333.
Abstract: Observed a total of 109 copulations in 6 male-female pairs from 4 species of large Felidae. The mean intromission durations were 3.0 sec for Asian leopards (Panthera pardus), 3.3 sec for African leopards (P. pardus), 12.9 sec for snow leopards (Uncia uncia), 2.3 sec for spotted jaguars (P. onca), 3.3 sec for black jaguars (P. onca), and 12.4 sec for Siberian tigers (P. tigris). Behavioral patterns were qualitatively similar across species; all displayed a copulatory pattern with no lock, no intravaginal thrusting, ejaculation on a single insertion, and multiple ejaculations. Whereas domestic cats are reported to assume a neck grip and to tread prior to insertion, these larger Felidae generally did so after intromission had been achieved. After copulation, females of some pairs swiped at the male and displayed a rolling after-reaction. (18 ref) (PsycINFO Database Record (c) 2000 APA, all rights reserved)(unassigned)
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Ale, S. B., Brown, J.S. (2009). Prey behavior leads to predator: a case study of the Himalayan tahr and the snow leopard in Sagarmatha (Mt. Everest) National Park, Nepal. Israel Journal of Ecology & Evolution, 55(4), 315–327.
Abstract: Rare, elusive predators offer few sightings, hindering research with small sample sizes and lack of experimentation. While predators may be elusive, their prey are more readily observed. Prey respond to the presence of a predator, and these fear responses may have population- and community-level consequences. Anti-predator behaviors, such as vigilance, allow us to sidestep the difficulty of direct field studies of large predators by studying them indirectly. Here we used a behavioral indicator, the vigilance behavior of the Himalayan tahr, the snow leopard’s main local prey, to reveal the distribution and habitat use of snow leopards in the Mt. Everest region of Nepal. We combined techniques of conventional field biology with concepts of foraging theory to study prey behavior in order to obtain insights into the predator’s ecology. The Himalayan tahr’s vigilance behavior correlates with the distribution of snow leopard signs. Tahr actually led us to six sightings of snow leopards. We conclude that behavioral indicators provided by prey offer a valuable tool for studying and monitoring stealthy and rare carnivores.
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Ming, M., Chundawat R.S., Jumabay, K., Wu, Y., Aizeizi, Q., & Zhu, M. H. (2006). Camera trapping of snow leopards for the photo capture rate and population size in the Muzat Valley of Tianshan Mountains. Acta Theriologica Sinica, 52(4), 788–793.
Abstract: The main purpose of this work was to study the use of infrared trapping cameras to estimate snow leopard Uncia uncia population size in a specific study area. This is the first time a study of this nature has taken place in China. During 71 days of field work, a total of 36 cameras were set up in five different small vales of the Muzat Valley adjacent to the Tomur Nature Reserve in Xinjiang Province, E80ø35' – 81ø00' and N42ø00' – 42ø10', elevation 2'300 – 3'000 m, from 18th October to 27th December 2005. We expended approximately 2094 trap days and nights total (c. 50'256 hours). At least 32 pictures of snow leopards, 22 pictures of other wild species (e.g. chukor, wild pig, ibex, red fox, cape hare) and 72 pictures of livestock were taken by the passive Cam Trakker (CT) train monitor in about 16 points of the Muzat Valley. The movement distance of snow leopard was 3-10 km/day. And the capture rate or photographic rate of snow leopard was 1.53%. Meanwhile, 20 transects were run and 31 feces sample were collected. According to 32 photos, photographic rate and sign survey after snowing on the spot, were about 5-8 individuals of snow leopards in the research area, and the minimum density of snow leopard in Muzat Valley was 2.0 – 3.2 individuals/100 km2. We observed the behavior of ibex for 77.3 hours, and found about 20 groups and a total of approximately 264 ibexes in the research area.
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Freeman, H., Braden, K. (1977). Zoo location as a factopr in the reproductive behavior of captive snow leopards, Uncia uncia. Zoological Garten J.F., 47(3/4), 280–288.
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Rana, B. S. (1997). Distinguishing kills of two large mammalian predators in Spiti Valley Himachal Pradesh. J.Bombay Nat.Hist.Soc, 94(3), 553.
Abstract: The author studied livestock killed by predators in the Spiti Valley, India, to determine what species had killed yaks, horses, donkeys, and other domestic animals. Eleven of the kills examined were made by snow leopards and six by the Tibetan wolf. Wolves were involved in surplus killings, while snow leopards kill as food is needed. lgh
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Ali, S. M. (1990). The Cats of India. Myforest, 26(3), 275–291.
Abstract: Describes the range, behaviour and ecology of lion Panthera leo, tiger P. tigris, leopard P. pardus, snow leopard P. uncia, clouded leopard Neofelis nebylosa and cheetah Acinonyx jubatus. -P.J.Jarvis
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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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Guerrero, D. (1998). Animal behavior concerns & solutions: snow leopard (Uncia uncia) evaluation, zoo. Anim.Keepers' Forum, 25(2), 56–58.
Abstract: The author offers advice on how a captive-raised snow leopard cub could be acclimated to humans so it could be used as a zoo “ambassador”. The cub had negative experiences with humans and lacked socialization with other animals and conspecifics. Methods of avoiding and redirecting the cub's aggressive behavior are suggested. lgh.
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Nolte-Wilson, B. (1990). Soveriegn of menaced realm: the snow leopard. Natura WWF-Pakistan Newsletter, 9(2), 3–9.
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Dzhanyspaev, A. D. (1991). Hunting Behavior of the Snow Leopard at the Alma-Atinski Nature Reserve (Vol. ix). Seattle: International Snow Leopard Trust.
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McVittie, R. (1978). Nursing behavior of snow leopard cubs. Applied-Animal-Ethology, 4(2), 159–168.
Abstract: Reports that a preliminary project on nursing behavior in 3 young snow leopards revealed 2 phases in suckling pattern: nonnutritive and nutritive. The latter was distinguished by stereotypic rhythmical movements of the ears associated with swallowing. The cubs also demonstrated a teat preference, but the adaptive significance of such preferences and the accompanying agonistic behavior were unclear. (27 ref) (PsycINFO Database Record (c) 2000 APA, all rights reserved)(unassigned)
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Reed-Smith, J., & Kumpf, M. (1998). Snow leopards (Uncia uncia): family group management alternatives. Anim.Keepers' Forum, 25(10), 386–391.
Abstract: The authors offer insights into creating family groups of snow leopards in zoos. The programs at the Denver Zoo, Denver, Colorado, and at John Ball Zoological Gardens, Grand Rapids, Michigan, are highlighted. lgh.
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Freeman, H. (1983). Behavior in adult pairs of captive snow leopards (Panthera uncia). Zoo Biology, 2(1), 1–22.
Abstract: Eight adult pairs of snow leopards (Panthera uncia) were observed for one to three years in the months December through March to determine the species' social and reproductive characteristics in captivity. To statistically examine the occurrence of behaviors as a function of estrus, the observation weeks were divided into three time blocks: before estrus, estrus, and after estrus. Using percentage of scan samples as an estimate of time spent in various behaviors, 16 behaviors and combined behavior categories were examined for (1) behaviors that differentiated successfully from unsuccessfully breeding pairs, (2) sex differences in behavior, (3) significant correlations between pair members, and (4) behaviors that showed time block effects. The rationale for identifying a behavioral profile of successful breeders in snow leopards was to aid zoos in their captive management programs by increasing their knowledge of the social behavior of this species. By finding correlates to breeding success, informed decisions on whether to change partners after a certain period of time, how to group the cats, and the optimum strategy for a survival plan can be made. (PsycINFO Database Record (c) 2000 APA, all rights reserved
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Fox, J. L., & Chundawat, R. S. (1988). Observations of snow leopard stalking, killing and feeding behavior. Mammalia, 52(1), 137–140.
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Schmidt, A. M., Hess, D. L., Schmidt, M. J., & Lewis, C. R. (1993). Serum concentrations of oestradiol and progesterone and frequency of sexual behaviour during the normal oestrous cycle in the snow leopard (Panthera uncia). J Reprod Fertil, 98(1), 91–95.
Abstract: Serum oestradiol and progesterone concentrations were measured at weekly intervals for six months, and correlated with daily behavioural observations in two adult female snow leopards (Panthera uncia). Three oestradiol peaks (> 21 pg ml-1; interval 3.6 weeks) were identified in a snow leopardess housed alone (two more were probably missed because of the weekly sampling schedule), and three oestradiol peaks were identified in a snow leopardess housed with a male as a breeding pair (interval 6 weeks). Daily frequencies of feline reproductive behaviour averaged 1.77 observations per observation period during weeks of high oestradiol and 0.62 during weeks of low oestradiol. Progesterone concentrations did not rise above baseline values (< 2 ng ml-1) in the isolated animal, but 6 weeks of high progesterone concentrations (4.9- 38.8 ng ml-1) was recorded in the paired snow leopardess following mating. No offspring were produced. Snow leopards were observed daily for an additional 4.5 years. Sexual behaviour peaks could be clearly identified from December through April, and average daily sexual behaviour scores were higher during these months than during the rest of the year. Intervals between sexual behaviour peaks for the isolated snow leopardess averaged 3.03 weeks. The sexual behaviour of the paired snow leopards decreased for 8-9 weeks following mating when no offspring were produced, and decreased for 13 weeks in one year when a single cub was born.
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Schaller, G. B. (1972). On meeting a Snow Leopard. Animal Kingdom, 75(1), 7–13.
Abstract: Discusses snow leopard distribution, ecology and conservation. Describes baiting (with a domestic goat) of a snow leopard and cub in a game reserve in Northern Pakistan. Incudes a description of the Leopard killing a goat, and observations over a week when the leopards were feeding on the goat baits.
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Rieger, I., & Peters, G. (1981). Observations on the mating and vocal behavior of snow leopards (Uncia-uncia) in zoological garden. Zeitschrift Fur Saugetierkunde International Journal of Mamamalian Biology, 46(1), 35–48.
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Matyushkin, E. N. (2000). Tracks and tracking techniques in studies of large carnivorous mammals. Zoologichesky Zhurnal, 79((4)), 412–429.
Abstract: In Russia, traditions of track observations and the use of tracking techniques in studying the ecology and behavior of mammals were founded by A.N. Formozov. An analytic review of his data on large carnivorous mammals (tiger, snow leopard, wolf, brown bear, wolverine, and others) is given. A special detailed observation of animals' tracks as a source of information on their life is shown only to start. The efficiency of track observations in various fields of studies, including counting animals, is estimated. The values of day and night distances for various animal species, given in literature, have never been properly substantiated methodically. The tracking method is the most effective in studying the use of the home range by animals, drawing the network of their movements and scent-marking behavior. The hunting behavior of large predators in dense forests is can only be deduced by observing their tracks. In some cases, the use of tracking has a distinct advantage over radio tracking. The main propositions are illustrated by the materials of the author obtained in various Russian regions (in forests of the northern Russian Plain and southern Far east) for 1958-1998.
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Molyukov M.I. (1989). Irbis.
Abstract: In a popular form it tells about snow leopard, its geographical distribution, behavioral patterns, food, enemies and competitors, hunting behavior, etc. Given are interesting data concerning the number of ibex killed during one hunt in eastern Pamir (25 30 ibexes), cases of snow leopard's attacking bears and so on. Snow leopard rarely preys on livestock, mainly sheep and goats. Young snow leopards are easily tamed. There are about 2,000 snow leopards in the USSR about 1,500 of them are in Kyrgyzstan.
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Panwar, H. S., Fox, J. L., Sinha, S. P., & Chundawat, R. S. (1986). Ecology of the Snow Loepard and Associated Prey in Central Ladakh.
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Oshmarin P.G. (1990). Traces in nature.
Abstract: Traces of vital activity of various animal species such as footprints, faeces, food remains, etc. are identified. It also provides information about hunting behavior of predators. Snow leopards would hunt along rather than in groups. Near the remains of prey they leave pieces of skin, skull of victim remaining untouched.
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Sapozhnikov G.N. (1976). Wild sheep in Tajikistan.
Abstract: The monograph provides data concerning taxonomy, morphology, and age variability of wild sheep. There described distribution, number, population composition, behavioral patterns, reproduction, predators and parasites. Besides, a matter of conservation and sustainable use of the species is discussed. Together with wolf, snow leopard is called an enemy of O. o. vignei and argali (O. o. polii).
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