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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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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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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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Koshkarev, E. P. (1984). Characteristics of snow leopard (Uncia uncia) movements in the Tien Shan. International Pedigree Book of Snow Leopards, 4, 15–21.
Abstract: Reports on a 3 yr winter study of snow leopard movements and activity, based on following tracks in the snow in Tien Shan Mountains of USSR. Travel route preference is examined with regard to snow and terrain characteristics, and prey abundance. Snow leopard kills of ibex and hare are noted
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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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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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Bykova E.A. (2004). Method of questionnaire design used for the collecting of primary data on threatened species with the example of snow leopard.
Abstract: Method of questionnaire design is used for long time successfully in the various fields of zoological research. This method is most significant for the collecting of data on threatened species. It can be applied together with standard inquest and survey methods without taking remarkable financial and temporal expenses. Such data can be assigned as the base for further planning of scientific investigations of the threatened species. In the result of survey, there were gathered 96 records of Snow Leopard and its tracks of the vital functions on Ugam, Pskem, Chatkal, Turkestan and Hissar ridges. Majority of records was made on Hissar ridge either on the area of Hissar reserve, either outside of protected area. There was collected data on distribution of Snow Leopard in Uzbekistan, on its territorial and food behavior, cases and causes of poaching. As a conclusion, it seems to be rational to use the method of questionnaire design among rangers of protected areas and local inhabitants for the collecting of primary information on threatened animal species. It would be optimal to gather such data every 3-4 years that would allow receiving the fresh comparable year-by-year information. Interpretation of questionnaire data should be made with certain prudence, taking into account subjectivity of collected information. Therefore during gathering of questionnaire data it is desirable personal attendance of researcher for more accurate definition of answers on the presented questions.
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Razmakhnin V.E. (1977). Siberian wild ibex.
Abstract: It provides a detailed description of biology, distribution, geographic variability, behavior, and locomotion features of ibex in the USSR. Its population was defined as 100,000 animals, main enemies being wolf, snow leopard, and golden eagle. Wolf mainly preys on ibex at the end of winter; old males, weakened during the heat mostly becoming a prey. Snow leopards prey on ibexes all year round. Golden eagles mostly prey on young ibexes.
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Lukarevskiy V.S. (2003). Peculiarities of communicative behavior of leopard, irbis, lynx, and caracal.
Abstract: It gives the description of communicative behavioral system (visual, olfactory and vocal elements) for two groups of large Felidae species such as leopard-irbis and lynx-caracal. General and specific behavioral regularities are given.
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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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