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Ale, S. B., & Karky, B. S. (2002). Observations on Conservation of Snow Leopards in Nepal.. Islt: Islt.
Abstract: The wild populations of snow leopards are threatened in Nepal. For their effective conservation, this paper seeks to build a strategy based not only on protected enclaves but also on landscapes, using an integrated grass-roots approach that essentially reduces poverty and addresses the needs of human beings and that of wildlife. Also equally relevant in places with a strong hold by religious and cultural authorities in the decision-making processes is the recognition and possible integration of cultural and traditional belief systems in overall snow leopard conservation schemes.
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Fox, J. (1989). A Review of the Status and Ecology of the Snow Leopard (Panthera uncia). International Snow Leopard Trust.
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Jackson, R., Roe, J., Wangchuk, R., & Hunter, D. (2006). Estimating Snow Leopard Population Abundance Using Photography and Capture-Recapture Techniques (Vol. 34).
Abstract: Conservation and management of snow leopards (Uncia uncial) has largely relied on anecdotal evidence and presence-absence data due to their cryptic nature and the difficult terrain they inhabit. These methods generally lack the scientific rigor necessary to accurately estimate population size and monitor trends. We evaluated the use of photography in capture-mark-recapture (CMR) techniques for estimating snow leopard population abundance and density within Hemis National Park, Ladakh, India. We placed infrared camera traps along actively used travel paths, scent-sprayed rocks, and scrape sites within 16-30 kmý sampling grids in successive winters during January and March 2003-2004. We used head-on, oblique, and side-view camera configurations to obtain snow leopard photographs at varying body orientations. We calculated snow leopard abundance estimates using the program CAPTURE. We obtained a total of 66 and 49 snow leopard captures resulting in 8.91 and 5.63 individuals per 100 trap nights during 2003 and 2004, respectively. We identified snow leopards based on the distinct pelage patters located primarily on the forelimbs, flanks, and dorsal surface of the tail. Capture probabilities ranged from 0.33 to 0.67. Density estimates ranged from 8.49 (SE+0.22) individuals per 100 kmý in 2003 to 4.45 (SE+0.16) in 2004. We believe the density disparity between years is attributable to different trap density and placement rather than to an actual decline in population size. Our results suggest that photographic capture-mark-recapture sampling may be a useful tool for monitoring demographic patterns. However, we believe a larger sample size would be necessary for generating a statistically robust estimate of population density and abundance based on CMR models.
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McCarthy, K., Fuller, T., Ming, M., McCarthy, T., Waits, L., & Jumabaev, K. (2008). Assessing Estimators of Snow Leopard Abundance (Vol. 72).
Abstract: The secretive nature of snow leopards (Uncia uncia) makes them difficult to monitor, yet conservation efforts require accurate and precise methods to estimate abundance. We assessed accuracy of Snow Leopard Information Management System (SLIMS) sign surveys by comparing them with 4 methods for estimating snow leopard abundance: predator:prey biomass ratios, capture-recapture density estimation, photo-capture rate, and individual identification through genetic analysis. We recorded snow leopard sign during standardized surveys in the SaryChat Zapovednik, the Jangart hunting reserve, and the Tomur Strictly Protected Area, in the Tien Shan Mountains of Kyrgyzstan and China. During June-December 2005, adjusted sign averaged 46.3 (SaryChat), 94.6 (Jangart), and 150.8 (Tomur) occurrences/km. We used
counts of ibex (Capra ibex) and argali (Ovis ammon) to estimate available prey biomass and subsequent potential snow leopard densities of 8.7 (SaryChat), 1.0 (Jangart), and 1.1 (Tomur) snow leopards/100 km2. Photo capture-recapture density estimates were 0.15 (n = 1 identified individual/1 photo), 0.87 (n = 4/13), and 0.74 (n = 5/6) individuals/100 km2 in SaryChat, Jangart, and Tomur, respectively. Photo-capture rates
(photos/100 trap-nights) were 0.09 (SaryChat), 0.93 (Jangart), and 2.37 (Tomur). Genetic analysis of snow leopard fecal samples provided minimum population sizes of 3 (SaryChat), 5 (Jangart), and 9 (Tomur) snow leopards. These results suggest SLIMS sign surveys may be affected by observer bias and environmental variance. However, when such bias and variation are accounted for, sign surveys indicate relative abundances similar to photo rates and genetic individual identification results. Density or abundance estimates based on capture-recapture or ungulate biomass did not agree with other indices of abundance. Confidence in estimated densities, or even detection of significant changes in abundance of snow leopard, will require more effort and better documentation.
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Chapron, G. (2005). Re-wilding: other projects help carnivores stay wild. Nature, 437, 318.
Abstract: Letter to Nature Editor, in response to: In their plea for bringing Pleistocene wildlife to the New World (“Re-wilding North America” Nature 436, 913–914; 2005), Josh Donlan and colleagues do not discuss successful efforts to ensure long-term survival of large carnivores in Africa and Asia. A few examples are given.
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Rothschild, B. M., Rothschild, C., & Woods, R. J. (1998). Inflammatory arthritis in large cats: An expanded spectrum of spondyloarthropathy. Journal of Zoo and Wildlife Medicine, 29(3), 279–284.
Abstract: Spondyloarthropathy was documented for the first time in 14 (3.7%) of 386 large cats, affecting eight species belonging to three genera. The limited distribution of joint erosions, associated with spine and sacroiliac joint pathology, was indistinguishable from that occurring in humans with spondyloarthropathy of the reactive type. This form of inflammatory arthritis is almost twice as common as osteoarthritis (for felids as a whole), and animal well-being may be enhanced by its recognition and by initiation of specific treatment.
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Wolf, M., & Ale, S. (2009). Signs at the Top: Habitat Features Influencing Snow Leopard Uncia Uncia Activity in Sagarmatha National Park, Nepal. Journal of Mammalogy, 90(3), 604–611.
Abstract: We used logistic regression to examine factors that affected the spatial distribution of sign (scrapes, feces, footprints, spray or scent marks, and rubbing sites) in a newly reestablished population of snow leopards (Uncia uncia) in Sagarmatha (Mount Everest) National Park, Nepal. Our results indicate that terrain and human activity were the most important factors determining the spatial distribution of leopard activity, whereas presence of their major prey species (Himalayan tahr [Hemitragus jemlahicus]) had only a moderate effect. This suggests that localities at which these animals are active represent a trade-off between suitable habitat and avoidance of potential risk from anthropogenic origins. However, the influence of prey presence was likely underestimated because of the methodology used, and likely weighed in the trade-off as well.
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Shi, K., Jun, Z. F. S., Zhigang, D., Riordan, P., & MacDonald, D. (2009). Reconfirmation of snow leopards in Taxkurgan Nature Reserve, Xinjiang, China. Oryx, 43(2), 169–170.
Abstract: China may hold a greater proportion of the global snow leopard Panthera uncia population than any other country, with the area of good quality suitable habitat, estimated at nearly 300,000 km2, comprising .50% of that available across the species' entire range. We can now reconfirm the presence of snow leopard in the Taxkurgan area of Xinjiang Province in north-west China after a period of 20 years.
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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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Johansson, O., Nyam, E., Lkhagvajav, P., Alexander, J. A., Samelius, G. (2023). Predation Patterns and Hunting Behaviour of Snow Leopards: Insights from an Ibex Hunt. Snow Leopard Reports, , 6–9.
Abstract: The hunting behaviours of the snow leopard (Panthera uncia) are poorly understood. In this note, we describe the successful hunt of an adult male ibex (Capra sibirica) by a known male snow leopard in Tost Mountains, Mongolia. The hunt started in a mountain slope close to three large boulders and progressed downhill for 115 m until it concluded at the bottom of a drainage. By comparing the habitat where the ibex was killed to the kill sites of 158 ibex and 17 argali (Ovis ammon) that were killed by GPS-collared snow leopards, we demonstrate that the majority (62%) of these kills occurred in drainages. We propose that in successful hunts, snow leopards commonly ambush from above, causing prey individuals to typically flee downhill. Thereby the prey maintain their momentum and it is not until they are slowed down upon reaching the bottom of the drainage that the snow leopards are able to subdue them.
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