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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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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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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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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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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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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. (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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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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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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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. (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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Fox, J. L. (1989). A review of the status and ecology of the snow leopard (Panthera uncia).
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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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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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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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Yanfa, L. (1994). The care, breeding and diseases of snow leopards in Qinghai, China. In J.L.Fox, & D.Jizeng (Eds.), (pp. 167–175). Usa: Islt.
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Yanfa, L. (1994). Snow leopard distribution, purchase locations and conservation in Qinghai Province, China. In J.L.Fox, & D.Jizeng (Eds.), (pp. 65–72). Usa: Islt.
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Wharton, D., & Mainka, S. A. (1994). Captive Management of the Snow Leopard. In J.L.Fox, & D.Jizeng (Eds.), (pp. 135–148). Usa: Islt.
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Tserendeleg, J. (1994). On Protection and Survey of Snow Leopards in Mongolia. In J.L.Fox, & D.Jizeng (Eds.), (pp. 43–46). Usa: Islt.
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Thapa, K., Rayamajhi, S. (2023). Anti-predator strategies of blue sheep (naur) under varied predator compositions: a comparison of snow leopard-inhabited valleys with and without wolves in Nepal. Wildlife Research, , 1–9.
Abstract: In Nepal, naur are usually the staple wild prey for the snow leopard, a solitary stalker hunter, and in some cases, for the wolf who hunts in a pack. We assumed that naur would adapt their anti-predatory responses to the presence of chasing and ambushing predators in the Manang Valley, where there are snow leopards and wolves, and in the Nar Phu valley, an area where there is only the snow leopard.
Aims. The aim of this study was to determine if there were differences in anti-predator strategies (vigilance, habitat selection and escape terrain) of naur in two valleys over two seasons, spring and autumn.
Methods. In spring 2019, we conducted a reconnaissance survey on the status of the naur and its habitat in the Manang and Nar Phu valleys of the Annapurna Conservation Area, Nepal. In spring and autumn 2020 and 2021, we observed 360 focal naur individuals (180 individuals in each valley), using the vigilance behaviour methodology to examine the behaviour of the naur.
Key results. There was little difference in the size of the naur groups between the Manang and Nar Phu valleys. The naur were twice as vigilant in Manang (15%), where there are snow leopards and wolves, as they were in Nar Phu (9%), with only snow leopards. The distance from the naur to escape cover was significantly shorter in Manang than in Nar Phu valley. Naur used significantly more rolling terrain in Nar Phu than in Manang. Conclusions. The return of wolves to the Manang valley may have resulted in an increase in the level of naur vigilance. Most likely, the wolves in Manang have already had an effect on the female-to-young-ratio, and this effect will possibly have important consequences for the naur population, as well as at the ecosystem level in the future. Other key determining factors, such as the climate crisis and changes in local resources, could have a significant impact on the naur population, indicating the need for more research. Implications. The findings of this study would provide valuable baseline information for the design of a science-based conservation strategy for conservation managers and scientists on naur, snow leopards and wolves.
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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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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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Sitnikov, P. (1988). The Death of a Snow Leopard. In L.Blomqvist (Ed.), (pp. 7–8). Helsinki, Finland.
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