Mallon, D. P. (1988). A Further Report on The Snow Leopard in Ladakh. In H.Freeman (Ed.), (pp. 89–97). India: Snow Leopard Trust and Wildlife Institute of India.
Abstract: A detailed knowledge of the ecology of a species is fundemental to the drawing up of effective conservation measures. One aim of the current project was to identify good areas of snow leopard habitatand evaluate them for possible inclusion in the Protected Area Network. Several good areas were surveyed and an outstanding area identified, and included in a report to the Chief Wildlife Warden.
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Anwar, M., Jackson, R., Nadeem, M., Janecka, J., Hussain, S., Beg, M., Muhammad, G., and Qayyum, M. (2011). Food habits of the snow leopard Panthera uncia (Schreber, 1775) in Baltistan, Northern Pakistan. European Journal of Wildlife Research, (3 March), 1–7.
Abstract: The snow leopard (Panthera uncia) inhabits the high, remote mountains of Pakistan from where very little information is available on prey use of this species. Our study describes the food habits of the snow leopard in the Himalayas and Karakoram mountain ranges in Baltistan, Pakistan. Ninety-five putrid snow leopard scats were collected from four sites in Baltistan. Of these, 49 scats were genetically confirmed to have originated from snow leopards. The consumed prey was identified on the basis of morphological characteristics of hairs recovered from the scats. It was found that most of the biomass consumed (70%) was due to domestic livestock viz. sheep (23%), goat (16%), cattle (10%), yak (7%), and cattle–yak hybrids (14%). Only 30% of the biomass was due to wild species, namely Siberian ibex (21%), markhor (7%), and birds (2%). Heavy predation on domestic livestock appeared to be the likely cause of conflict with the local inhabitants. Conservation initiatives should focus on mitigating this conflict by minimizing livestock losses.
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Suryawanshi, K. R., Bhatnagar, Y., & Mishra, C. (2009). Why should a grazer browse? Livestock impact on winter resource use by bharal Pseudois nayaur
. Oecologia, , 1–10.
Abstract: Many mammalian herbivores show a temporal diet variation between graminoid-dominated and browse dominated diets. We determined the causes of such a diet shift and its implications for conservation of a medium sized ungulate-the bharal Pseudois nayaur. Past studies show that the bharal diet is dominated by graminoids (>80%) during summer, but the contribution of graminoids declines to about 50% in winter. We tested the predictions generated by two alternative hypotheses explaining the decline: low graminoid availability during winter causes bharal to include browse in their diet; bharal include browse, with relatively higher nutritional quality, in their diet to compensate for the poor quality of graminoids during winter. We measured winter graminoid availability in areas with no livestock grazing, areas with relatively moderate livestock grazing, and those with intense livestock grazing pressures. The chemical composition of plants contributing to the bharal diet was analysed. The bharal diet was quantiWed through signs of feeding on vegetation at feeding locations. Population structures of bharal populations were recorded using a total count method. Graminoid availability was highest in areas without livestock grazing, followed by areas with moderate and intense livestock grazing. The bharal diet was dominated by graminoids (73%) in areas with highest graminoid availability. Graminoid contribution to the bharal diet declined monotonically (50, 36%) with a decline in graminoid availability. Bharal young to female ratio was 3 times higher in areas with high graminoid availability than areas with low graminoid availability. The composition of the bharal winter diet was governed predominantly by the availability of graminoids in the rangelands. Our results suggest that bharal include more browse in their diet during winter due to competition from livestock for graminoids. Since livestock grazing reduces graminoid availability, creation of livestock-free areas is necessary for the conservation of grazing species such as the bharal and its predators including the endangered snow leopard in the Trans-Himalaya.
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Guggisberg, C. A. W. (1975). Snow Leopard, Ounce.. New York: Taplinger Publication Co. Inc.
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Kinoshita, K., Inada, S., Seki, K., Sasaki, A., Hama, N., Kusunoki, H. (2011). Long-Term Monitoring of Fecal Steroid Hormones in Female Snow Leopards (Panthera uncia) during Pregnancy or Pseudopregnancy. PLoS ONE, 6(5), e19314. doi:10.1371/journal.pone.0019314.
Abstract: Knowledge of the basic reproductive physiology of snow leopards is required urgently in order to develop a suitable management conditions under captivity. In this study, the long-term monitoring of concentrations of three steroid hormones in fecal matter of three female snow leopards was performed using enzyme immunoassays: (1) estradiol-17β, (2) progesterone and (3) cortisol metabolite. Two of the female animals were housed with a male during the winter breeding season, and copulated around the day the estradiol-17β metabolite peaked subsequently becoming pregnant. The other female was treated in two different ways: (1) first housed with a male in all year round and then (2) in the winter season only. She did not mate with him on the first occasion, but did so latter around when estradiol-17β metabolite peaked, and became pseudopregnant. During pregnancy, progesterone metabolite concentrations increased for 92 or 94 days, with this period being approximately twice as long as in the pseudopregnant case (31, 42, 49 and 53 days). The levels of cortisol metabolite in the pseudopregnant female (1.35 µg/g) were significantly higher than in the pregnant females (0.33 and 0.24 µg/g) (P<0.05). Similarly, during the breeding season, the levels of estradiol-17β metabolite in the pseudopregnant female (2.18 µg/g) were significantly higher than those in the pregnant females (0.81 and 0.85 µg/g) (P<0.05). Unlike cortisol the average levels of estradiol-17β during the breeding season were independent of reproductive success.
The hormone levels may also be related to housing conditions and the resulting reproductive success in female leopards. The female housed with a male during the non-breeding season had high levels of cortisol metabolites and low levels of estradiol-17β in the breeding season, and failed to become pregnant. This indicates that housing conditions in snow leopards may be an important factor for normal endocrine secretion and resulting breeding success.
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Jackson, R., Roe, J., Wangchuk, R., & Hunter, D. (2005). Surveying Snow Leopard Populations with Emphasis on Camera Trapping: A Handbook. Sonoma, California: The Snow Leopard Conservancy.
Abstract: This handbook provides an introduction to snow leopard population survey techniques, followed by a detailed account of camera trapping methods.During the 2002 through 2004 winter field seasons, the Snow Leopard Conservancy experimented with infrared camera trapping techniques to define a methodology suitable for the high altitude environment.
In 2001 and 2002, much of our time was spent familiarizing ourselves with various infrared camera traps, their operation and setup, and comparing the effectiveness of different models and sensor types. We placed infrared camera traps along frequently used travel corridors at or near scent-sprayed rocks (rock scents) and scrape sites within 16 km2 sampling cells between January and March in 2003 and 2004. A total of 66 and 49 captures of snow leopards were tallied during 2003 and 2004, resulting in an overall capture success of 8.91 and 5.63 individuals per 100 trap-nights, respectively. Capture probabilities ranged from 0.33 to 0.46. Density estimates ranged from 8.49 ± 0.22 individuals per 100 km2 in 2003 to 4.45 ± 0.16 in 2004, with the disparity between years largely attributed to different trapping densities. Snow leopard abundance estimates were calculated using the computer program CAPTURE.
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Jackson, R., Roe, J., Wangchuk, R., & Hunter, D. (2005). Surveying Snow Leopard Populations with Emphasis on Camera Trapping: A Handbook. Sonoma, California: The Snow Leopard Conservancy.
Abstract: This handbook provides an introduction to snow leopard population survey techniques, followed by a detailed account of camera trapping methods.During the 2002 through 2004 winter field seasons, the Snow Leopard Conservancy experimented with infrared camera trapping techniques to define a methodology suitable for the high altitude environment.
In 2001 and 2002, much of our time was spent familiarizing ourselves with various infrared camera traps, their operation and setup, and comparing the effectiveness of different models and sensor types. We placed infrared camera traps along frequently used travel corridors at or near scent-sprayed rocks (rock scents) and scrape sites within 16 km2 sampling cells between January and March in 2003 and 2004. A total of 66 and 49 captures of snow leopards were tallied during 2003 and 2004, resulting in an overall capture success of 8.91 and 5.63 individuals per 100 trap-nights, respectively. Capture probabilities ranged from 0.33 to 0.46. Density estimates ranged from 8.49 ± 0.22 individuals per 100 km2 in 2003 to 4.45 ± 0.16 in 2004, with the disparity between years largely attributed to different trapping densities. Snow leopard abundance estimates were calculated using the computer program CAPTURE.
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Simon, N., Geroudet, P. (1970). Last Survivores: The Natural History of Animals in Danger of Extinction. (pp. 127–131). New York: The World Publishing Company.
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Shrestha, R., Wegge, P., & Koirala, R. A. (2005). Summer diets of wild and domestic ungulates in Nepal Himalaya. Journal of Zoology, 266, 111–119.
Abstract: The selection of summer forage by three sympatric ungulates in the Damodar Kunda region of upper Mustang in
north Nepal was studied to assess the extent of food overlap between them. To compare their diets, a microhistological technique of faecal analysis was used, adjusted for inherent biases by comparing it with bite-count data obtained in domestic goats. Tibetan argali Ovis ammon hodgsoni, naur (blue sheep or bharal) Pseudois nayaur and domestic goat Capra hircus consumed mostly forbs, graminoids and browse, respectively. The proportions of food items in their diets were significantly different both at the plant species (P<0.02) and at the forage category level (P<0.001). Except for sharing three common plants (Agrostis sp., Stipa sp. and Potentilla fruticosa), dietary overlap at the species level was quite low. At the forage category level, naur and domestic goat overlapped more than the other ungulate pairs. Although all three species were opportunistic, mixed feeders, argali was a more selective forb specialist grazer than the other two ungulates. Owing to some spatial separation and little dietary overlap, interspecific competition for summer forage was low. If animal densities increase, however, goats are expected to compete more with naur than with argali because of their more similar diets. Owing to differences in forage selection by argali and naur throughout their large geographical ranges, reflecting adaptations to local ecological conditions, inferences regarding forage competition between domestic livestock and these two wild caprins need to be made from local, site-specific studies, rather than from general diet comparisons.
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Karanth, K. U., Nichols, J.D., Seidensticker, J., Dinerstein, E., David Smith, J.L., McDougal, C., Johnsingh, A.J.T., Chundawat, R.S., Thapar, V. (2003). Science deficiency in conservation practice: the monitoring of tiger populations in India. Animal Conservation, 6, 141–146.
Abstract: Conservation practices are supposed to get refined by advancing scientific knowledge. We study this phenomenon in the context of monitoring tiger populations in India, by evaluating the ‘pugmark census method’ employed by wildlife managers for three decades. We use an analytical framework of modern animal population sampling to test the efficacy of the pugmark censuses using scientific data on tigers and our field observations. We identify three critical goals for monitoring tiger populations, in order of increasing sophistication: (1) distribution mapping, (2) tracking relative abundance, (3) estimation of absolute abundance. We demonstrate that the present census-based paradigm does not work because it ignores the first two simpler goals, and targets, but fails to achieve, the most difficult third goal. We point out the utility and ready availability of alternative monitoring paradigms that deal with the central problems of spatial sampling and observability. We propose an alternative sampling-based approach that can be tailored to meet practical needs of tiger monitoring at different levels of refinement.
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