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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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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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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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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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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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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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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Fox, J. L. (1989). A review of the status and ecology of the snow leopard (Panthera uncia).
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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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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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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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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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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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Freeman, H. (1980). Breeding and behavior of the snow leopard.
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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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Hansen, J. (1980). The snow leopard study, part one.
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Chubykina, H. L., Shilo, R.A. (1981). A study of diurnal activity rhythms in snow leopards and lynx (Panthera uncia and Felix lynx) at Novosibirsk Zoo. International Zoo Yearbook, 21, 193–196.
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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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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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Ahlborn, G., & Jackson, R. (1987). Marking in Wild Snow Leopards: A preliminary assesment (Vol. No. 13). Seattle: Islt.
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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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Zhirjakov, V. A. (1990). On the ecology of the snow leopard in the Zailisky-Alatau (Northern Tien Shan). Int Ped Book of Snow Leopards, 6, 25–30.
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Zakhidov T.Z.Meklenburtsev R.N., B. O. P. (1971). Snow leopard Uncia uncia Schreb. Distribution of fauna elements over Central Asia (Vol. Vol. 2. Vertebrate animals.).
Abstract: Snow leopard inhabits the mountainous ecosystems from Tarbagatai to Hissar and Pamir. It feeds upon large animals such as ibex, argali, roe deer, and sometimes domestic sheep, rodents, and birds (most frequently snow cock). The skin of this animal is not of significant value and is rarely an item of trade. In many countries, zoos will readily buy snow leopards. There is no danger for a man to catch snow leopard since even being wounded during a hunt, the animal would never attack the man. An encounter with snow leopard in the mountains will always end safely for human being, as it is always first to spot a man and go away unnoticed.
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