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Freeman, H. (1980). Breeding and behavior of the snow leopard.
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Freeman, H. (1982). Characteristics of the social behavior in the snow leopard. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 117–120). Helsinki: Helsinki Zoo.
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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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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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Frueh, R. (1968). A note on breeding snow leopards at the Saint Louis Zoo. Int.Zoo Yearbook, 8, 74–76.
Abstract: Breif comments on physical characteristics of the young, care and reproductive behavior of snow leopards
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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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Gronberg, E. (2011). Movement patterns of snow leopard (Panthera uncia) around kills based on GPS location clusters. Master's thesis, , .
Abstract: Research concerning movement patterns of wild animals has been advancing since GPS technology arrived. But studying the snow leopard (Panthera uncia) is still difficult because of the harsh territory it inhabits in Central Asia. This study took place in south Gobi, Mongolia, and aimed to estimate the time spent at kills and the maximum distance away from kills between visits. Snow leopards were monitored with GPS collars that took a location every five or seven hours. Potential kill sites were established by identifying clusters of GPS-locations in ArcGIS and visited in the field for confirmation. ArcGIS was used to calculate the distance between cluster and GPS-locations. I used two buffer zones (100 m and 500 m radius) to define the time snow leopards spent at kills. It was found that snow leopard age and prey category affected time spent at kills and also that snow leopard sex together with prey category affected the maximum distance moved away from kills between visits. Season had no significant effect on either time at kills or distance moved away from kills between visits. Snow leopards spent on average 3.2 days at their kills in the 100 m buffer zone and 3.5 days at their kills in the 500 m buffer zone. Subadults stayed longer at kills than adults and animals of both age categories spent longer time on larger prey. The mean maximum distance moved away from kills between visits was 179 m in the 100 m buffer zone and 252 m in the 500 m buffer zone. Female snow leopards moved further away from kills between visits than male snow leopards. Both the number of days spent on kills and maximum distance moved away from kills between visits increased when kills consisted of more than one animal. This study has provided some basic information on snow leopard behaviors around their kills but also highlights the need to monitor more snow leopards before more solid conclusions can be drawn as this study was based on based on a relatively small sample.
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Gruisen, J. V. (1993). Interaction Between Wild Dogs and Snow Leopards in Ladakh (Vol. xi). Seattle: Islt.
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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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Hansen, J. (1980). The snow leopard study, part one.
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Hillard, D. (1985). Update on the Himalayan Snow Leopard Project (Vol. No. 8). Seattle: Islt.
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Hunter, D. (1996). Mongolian-American Snow Leopard Project (Vol. xiv). Seattle: International Snow Leopard Trust.
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Ishunin G.I. (1961). Irbis, or snow leopard Felis (Uncia) uncia S¤hr†b†a 1778 (Vol. Vol. 3.).
Abstract: It describes diagnostic signs and taxonomy of snow leopard as well as its distribution, behavioral patterns and use in Uzbekistan. This predator inhabits the Ugam, Pskem, Chatkal, Turkistan, and Gissar ridges. It mainly preys on ibex, and marmots, vole-mouse, and snow-cocks. Sometimes it attacks domestic sheep. Snow leopard is of low commercial value. The cost of skin is 4 roubles 70 kopecks. Only a few skins are purchased.
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Jack, Jill, Jackson, P., Wharton, D., & Jackson, R. Snow leopard, Ucia uncia.
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Jackson, R. (1992). SSC Plan for Snow Leopard.
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Jackson, R. (2000). Linking Snow Leopard Conservation and People-Wildlife Conflict Resolution, Summary of a multi-country project aimed at developing grass-roots measures to protect the endangered snow leopard from herder retribution. Cat News, 33, 12–15.
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Jackson, R. (2000). The Snow Leopard Conservancy, Dedicated to demonstrating innovative, grassroots measures that lead local shepherds to become better stewards of the endangered snow leopard, its prey and habitat.
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Jackson, R., & Ahlborn, G. (1987). Observation on Movements and Home Range of the Snow Leopard, (Panthera Uncia) In the Langu Gorge, West Nepal (Vol. No. 13). Seattle: Islt.
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Jackson, R., & Ahlborn, G. (1989). Snow Leopards in Nepal-home range and movements. National Geographic Res., 5, 161–175.
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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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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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Jackson, R. M., & Ahlborn, G. (1988). Observations on the Ecology of Snow Leopard in West Nepal. In H.Freeman (Ed.), (pp. 65–87). India: Snow Leopard Trust and Wildlife Institute of India.
Abstract: This summary of a four year field study by Jackson and Ahlborn begging in 1982 and concluding in 1985, discusses behaviour, trapping and tracking techniques, home range, activity patterns, prey and habitat and survey methods.
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Johansson, O., Ausilio, G., Low, M., Lkhagvajav, P., Weckworth,
B., Sharma, K. (2020). The timing of breeding and independence for snow leopard females
and their cubs. Mammalian Biology, .
Abstract: Significant knowledge gaps persist on snow leopard demography
and reproductive behavior. From a GPS-collared population in Mongolia,
we estimated the timing of mating, parturition and independence. Based
on three mother–cub pairs, we describe the separation phase of the cub
from its mother as it gains independence. Snow leopards mated from
January–March and gave birth from April–June. Cubs remained with their
mother until their second winter (20–22 months of age) when cubs started
showing movements away from their mother for days at a time. This
initiation of independence appeared to coincide with their mother mating
with the territorial male. Two female cubs remained in their mothers’
territory for several months after initial separation, whereas the male
cub quickly dispersed. By comparing the relationship between body size
and age of independence across 11 solitary, medium-to-large felid
species, it was clear that snow leopards have a delayed timing of
separation compared to other species. We suggest this may be related to
their mating behavior and the difficulty of the habitat and prey capture
for juvenile snow leopards. Our results, while limited, provide
empirical estimates for understanding snow leopard ecology and for
parameterizing population models.
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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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Korytin S.A. (1986). Animal's behavior near attractions. Animal's reaction to chasing with dogs. Animal behavior and traps.
Abstract: It describes trophic behavior of the cat family species (lion, tiger, leopard, snow leopard, cheetah, caracal, reed cat, wild cat and domestic cat), their reaction to dog-chasing and behavioral patterns when trapped. Snow leopards (Uncia uncia) sometime eat dead animals. After killing the prey they take it away. Irbis eats the carcass, half-risen on front limbs, beginning from the chest and front limbs or lower part of belly, usually not touching intestines. It eats slowly and spends a lot of time near the carcass and returns to the carcass several times. Known are cases that two snow leopards, or a snow leopard and wolf eating the prey together. Snow leopard usually keeps birds off the carcass. If a man approaches snow leopard normally goes away, sometimes putting up with his close presence. Escaping from dogs, snow leopard was seen to plunge into the river. When trapped, snow leopard rather easily surrenders to man.
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