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Hunter, D. (1996). Mongolian-American Snow Leopard Project (Vol. xiv). Seattle: International Snow Leopard Trust.
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Fox, J. L. (1989). A review of the status and ecology of the snow leopard (Panthera uncia).
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Schaller, G. B. (1980). Stones of Silence: Journeys in the Himalaya. New York: Viking Press.
Abstract: Anecdotal description of wildlife field studies in the Himalaya, including information on snow leopard natural history and an encounter with snow leopards in Pakistan.
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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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Schaller, G. B. (1977). Mountain Monarchs: Wild Sheep and Goats of the Himalaya (Wildlife Behavior & Ecology). Chicago: University of Chicago Press.
Abstract: Describes snow leopard status and field observations from studies in Pakistan and Nepal. Review provides some data on snow leopard marking behavior, social relations, food habits and predator behavior.
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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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Rieger, I. (1980). Some difficulty breeding ounces, (Uncia uncia) at zoological gardens. Int.Ped Book of Snow Leopards, 2, 76–95.
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Rieger, I. (1978). Scent marking behaviour of ounces, Uncia uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 1 (Vol. 1, pp. 78–103). Helsinki: Helsinki Zoo.
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Pokrovski, V. S. (1976). The Snow Leopard Large Predators. Moscow.
Abstract: Detailed review of snow leopard distribution and abundance, behavior, ecology,captive population and conservation measures in the Soviet Union. Estimates a snow leopard population of 300 +/- 150.
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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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O'Connor, T., & Freeman, H. (1982). Maternal behavior and behavioral development in the captive snow leopard (Panthera uncia). In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 103–110). Helsinki: Helsinki Zoo.
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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. (1992). SSC Plan for Snow Leopard.
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Ming, M. (2006). Camera trapping on snow leopards in the Muzat Valley, Reserve, Xinjiang, P.R. China (October-December 2005).
Abstract: The main purpose of this work was to study the use of infrared trapping cameras to estimate Snow Leopard 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 Muzat Valley adjacent to the Tomur Nature Reserve in Xinjiang Province. We expended approximately 2094 trap days total. At least 32 pictures of Snow Leopards, 22 pictures of other wild species and 72 pictures of livestock were taken in the Muzat Valley. Meanwhile, 20 transects were run and 31 feces sample were collected. We also observed the behavior of ibex for 77.3 hours and found a total of approximately 264 ibexes in the research area.
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Meiers, S. T. (1992). Habitat use by captive puma (Felis concolor) and snow leopards (Pathera uncia) at the Lincoln Park Zoo, Chicago, Illinois. Ph.D. thesis, DePaul University, .
Abstract: Between May 1990 and January 1991, behavioral observations were made of two captive pumas (Felis concolor Linnaeus), and two captive snow leopards (Panthera uncia Schreber) in their outdoor exhibits at the Lincoln Park Zoological Gardens, Chicago, Illinois. Behaviors compared within and between species included: 1) time spend in the different habitat types; 2) time budgets for the different behaviors: laying, moving, sitting, standing, crouching, in the tree, drinking, urinating, defecating, within their inside dens, and “behavior not determined” when the identity or behavior of the individuals could not be determined; and 3) mobility of the animals within their exhibits. Also examined were: 4) preferences for different habitat types; 5) recommendations for future exhibit designs. Both species located themselves within their exhibits in a non-random manner. The majority of cats' time was spent in elevated locations (i.e., gunite ledges approximately 1-5.5 m above ground-level). Snow leopards exhibited this tendency to a greater extent than did the pumas. Both species also spent the majority of their time in the lying-down behavior; again snow leopards displayed this tendency significantly more than the pumas. Pumas were highly mobile and changed locations and behaviors in their exhibit significantly more than the snow leopards. No significant differences were noted between conspecifics in regard to habitat type preference, or mobility within the exhibit. Suggestions for future exhibit design include elevated locations for the cats to lay and look around within and outside their exhibits, caves for access to shade or relief from inclement weather, and ground surfaces to move about on. Features for exhibit design should take into consideration the natural habitat of the cat to occupy the exhibit.
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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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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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Kuznetsnov, G. U., & Matyushkin, E. N. (1980). The snow leopard hunts. Int.Ped.Book of Snow Leopards, 11, 44–48.
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Sloane, A., Kelly, C., McDavitt, S., & Marples, N. (1998). Big cats in captivity: a quantitative analysis of enrichment. Adv.Etho, 33, 43.
Abstract: Studies on three species of big cats at Dublin Zoo have led to firm conclusions about the effects of certain forms of enrichment, some of which will be presented here. Lions, jaguars, and snow leopards were studied over two years and their behaviours quantified using focal animal sampling during selected hours during daylight. By comparison of these activity budgets with and without the enrichments being present, it was possible to identify the exact behavioural changes caused by each enrichment method, and to quantify these changes. In this contribution we present results showing that the presence of a platform in both lion and jaguar enclosures dramatically reduced stereotypic pacing behaviour. We will demonstrate that the effects of short term enrichment devices may have a wide range of effects on behaviours which outlast the presence of the stimulus. For instance scents added to the cage, or food/play items such as horse hides, hidden fish or ice-blocks often reduce pacing and increase resting later in the day, even after the cats have ceased using the enrichment items. This reduction in pacing and increase in resting time often meant that the amount of the enclosure used per hour was actually reduced with the presence of new stimuli, as result opposite to what might have been expected. The results of these studies will be discussed in relation to effective animal management.
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Subbotin, A. E., & Istomov, S. V. (2009). The population status of snow leopards Uncia uncia (Felidae, Carnivora) in the western Sayan Mountain Ridge. Doklady Biologicl Sciences, 425, 183–186.
Abstract: The snow leopard (Uncia uncial Schreber, 1776) is the most poorly studied species of the cat family in the world and, in particular, in Russia, where the northern periphery of the species area (no more than 3% of it) is located in the Altai-Hangai-Sayan range [1]. It is generally known that the existing data on the Russian part of the snow leopard population have never been a result of targeted studies; at best, they have been based on recording the traces of the snow leopard vital activity [2]. This is explained by the snow leopard's elusive behavior, inaccessibility of its habitats for humans, and its naturally small total numbers in the entire species area. All published data on the population status of the snow leopard in Russia, from the first descriptions of the species [3-6] to the latest studies [7, 8] are subjective, often speculative, and are not confirmed by
quantitative estimates. It is obvious, however, that every accurate observation of this animal is of particular interest [9]. The purpose of our study was to determine the structure and size of the population group presumably inhabiting the Western Sayan mountain ridge at the northern boundary of the species area
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Dang, H. (1967). The snow leopard and its prey. The Cheetal, 11, 47–58.
Abstract: Discusses distribution and habitat of snow leopard in India. Estimates population of 200-400 in entire Himalayan region. Reports seventeen occasions of observing snow leopards in the wild, one involving the killing of Himalayan thar. Discusses snow leopard hunting methods and food habits, and provides evidence of predation from examination of 17 snow leopard kills.
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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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Burgener, N., Gusset, M., & Schmid, H. (2008). Frustrated appetitive foraging behavior, stereotypic pacing, and fecal glucocorticoid levels in snow leopards (Uncia uncia) in the Zurich Zoo (Vol. 11).
Abstract: This study hypothesized that permanently frustrated, appetitive-foraging behavior caused the stereotypic pacing regularly observed in captive carnivores. Using 2 adult female snow leopards (Uncia uncia), solitarily housed in the Zurich Zoo, the study tested this hypothesis experimentally with a novel feeding method: electronically controlled, time-regulated feeding boxes. The expected result of employing this active foraging device as a successful coping strategy was reduced behavioral and physiological measures of stress, compared with a control-feeding regime without feeding boxes. The study assessed this through behavioral observations and by evaluating glucocorticoid levels noninvasively from feces. Results indicated that the 2 snow leopards did not perform successful coping behavior through exercising active foraging behavior or through displaying the stereotypic pacing. The data support a possible explanation: The box-feeding method did not provide the 2 snow leopards with the external stimuli to satisfy their appetitive behavioral needs. Moreover, numerous other factors not necessarily or exclusively related to appetitive behavior could have caused and influenced the stereotypic pacing.
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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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Ahlborn, G., & Jackson, R. (1987). Marking in Wild Snow Leopards: A preliminary assesment (Vol. No. 13). Seattle: Islt.
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