Li, J., Yin, H., Wang, D., Jiagong, Z., Lu, Zhi. (2013). Human-snow leopard conflicts in the Sanjiangyuan Region of the Tibetan Plateau. Biological Conservs, (166), 118–123.
Abstract: Conflicts between humans and snow leopards are documented across much of their overlapping distribution
in Central Asia. These conflicts manifest themselves primarily in the form of livestock depredation
and the killing of snow leopards by local herders. This source of mortality to snow leopards is a key conservation concern. To investigate human-snow leopard conflicts in the Sanjiangyuan Region of the Tibetan Plateau, we conducted household interviews about local herders’ traditional use of snow leopard
parts, livestock depredation, and overall attitudes towards snow leopards. We found most respondents
(58%) knew that snow leopard parts had been used for traditional customs in the past, but they claimed
not in the past two or three decades. It may be partly due to the issuing of the Protection of Wildlife Law
in 1998 by the People’s Republic of China. Total livestock losses were damaging (US$ 6193 per household
in the past 1 year), however snow leopards were blamed by herders for only a small proportion of those
losses (10%), as compared to wolves (45%) and disease (42%). Correspondingly, the cultural images of
snow leopards were neutral (78%) and positive (9%) on the whole. It seems that human-snow leopard
conflict is not intense in this area. However, snow leopards could be implicated by the retaliatory killing
of wolves. We recommend a multi-pronged conservation program that includes compensation, insurance
programs, and training local veterinarians to reduce livestock losses.
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LI. J, W. A. N. G. D., YIN. H, ZHAXI. D, JIAGONG. Z, SCHALLER. G. B, MISHRA. C, MCCARTHY. T. M, WANG. H, WU. L, XIAO. L, BASANG. L, ZHANG. Y, ZHOU. Y, LU. Z. (2013). Role of Tibetan Buddhist Monasteries in Snow Leopard Conservation. Conservation Biology, 00, 1–8.
Abstract: The snow leopard (Panthera uncia) inhabits the rugged mountains in 12 countries of Central Asia,
including the Tibetan Plateau. Due to poaching, decreased abundance of prey, and habitat degradation, it was listed as endangered by the International Union for Conservation of Nature in 1972. Current conservation strategies, including nature reserves and incentive programs, have limited capacities to protect snow leopards. We investigated the role of Tibetan Buddhist monasteries in snow leopard conservation in the Sanjiangyuan region in China’s Qinghai Province on the Tibetan Plateau. From 2009 to 2011, we systematically surveyed snow leopards in the Sanjiangyuan region. We used the MaxEnt model to determine the relation of their presence to environmental variables (e.g., elevation, ruggedness) and to predict snow leopard distribution. Model results showed 89,602 km2 of snow leopard habitat in the Sanjiangyuan region, of which 7674 km2 lay within Sanjiangyuan Nature Reserve’s core zones. We analyzed the spatial relation between snow leopard habitat and Buddhist monasteries and found that 46% of monasteries were located in snow leopard habitat and 90% were within 5 km of snow leopard habitat. The 336 monasteries in the Sanjiangyuan region could protect more snow leopard habitat (8342 km2) through social norms and active patrols than the nature reserve’s core zones. We conducted 144 household interviews to identify local herders’ attitudes and behavior toward snow leopards and other wildlife. Most local herders claimed that they did not kill wildlife, and 42% said they did not kill wildlife because it was a sin in Buddhism. Our results indicate monasteries play an important role in snow leopard conservation. Monastery-based snow leopard conservation could be extended to other Tibetan Buddhist regions that in total would encompass about 80% of the global range of snow leopards.
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Maheshwari, A., Sharma, D., Sathyakumar, S. (2013). Snow Leopard (Panthera Uncia) surveys in the Western Himalayas, India. Journal of Ecology and Natural Environmnet, 5(10), 303–309.
Abstract: We conducted surveys above 3000 m elevation in eight protected areas of Uttarakhand and Himachal Pradesh. These surveys provide new information on snow leopard in Uttarakhand on the basis of indirect evidence such as pugmark and scat. Snow leopard evidence (n = 13) were found between 3190 and 4115 m elevation. On an average, scats (n = 09) of snow leopard were found for every 56 km walked and pugmarks (n = 04) for every 126 km walked. Altogether, about 39% of the evidence were found on the hill-slope followed by valley floor (30%), cliff (15%) and 8% from both stream bed and scree slope. Genetic analysis of the scats identified three different individuals by using snow leopard specific primers. Snow leopard-human conflicts were assessed through questionnaire based interviews of shepherds from Govind Pashu Vihar Wildlife Sanctuary, Askot Wildlife Sanctuary and Nanda Devi Biosphere Reserve areas of Uttarakhand. Surveys revealed that livestock depredation (mule, goat and sheep) is the only cause of snow leopard-human conflicts and contributed 36% of the diet of snow leopard. Blue sheep and rodents together comprised 36.4% of the total diet. We found that 68.1% of the surveyed area was used for pastoral activities in Uttarakhand and Himachal Pradesh and 12.3% area was under tourism, defence and developmental activities.
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Lovari, S., Minder, I., Ferretti, F., Mucci, N., Randi, E., Pellizzi, B. (2013). Common and snow leopards share prey, but not habitats: competition avoidance by large predators. Journal of Zoology, 291, 127–135.
Abstract: Resource exploitation and behavioural interference underlie competition among
carnivores. Competition is reduced by specializing on different prey and/or spatiotemporal
separation, usually leading to different food habits. We predicted that
two closely related species of large cats, the endangered snow leopard and the
near-threatened common leopard, living in sympatry, would coexist through
habitat separation and exploitation of different prey species. In central Himalaya,
we assessed (2006–2010) habitat and diet overlap between these carnivores. The
snow leopard used grassland and shrubland, whereas the common leopard
selected forest. Contrary to our prediction, snow leopard and common leopard
preyed upon similar wild (Himalayan tahr, musk deer) and domestic species (Bos
spp., dogs). Dietary overlap between snow leopard and common leopard was 69%
(yearly), 76% (colder months) and 60% (warmer months). Thus, habitat separation
should be the result of other factors, most likely avoidance of interspecific
aggression. Habitat separation may not always lead to the use of different prey.
Avoidance of interspecific aggression, rather than exploitation of different
resources, could allow the coexistence of potentially competing large predators.
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Lovari, S., Ventimiglia, M., Minder, I. (2013). Food habits of two leopard species, competition, climate change and upper treeline: a way to the decrease of an endangered species? Ethology Ecology & Evolution, 25(4), 305–318.
Abstract: For carnivore species, spatial avoidance is one of the evolutionary solutions to
coexist in an area, especially if food habits overlap and body sizes tend to coincide.
We reviewed the diets of two large cats of similar sizes, the endangered snow leopard
(Panthera uncia, 16 studies) and the near-threatened common leopard (Panthera par-
dus, 11 studies), in Asia. These cats share ca 10,000 km2 of their mountainous range,
although snow leopards tend to occur at a significantly higher altitude than common
leopards, the former being a cold-adapted species of open habitats, whereas the latter
is an ecologically flexible one, with a preference for woodland. The spectrum of prey
of common leopards was 2.5 times greater than that of snow leopards, with wild prey
being the staple for both species. Livestock rarely contributed much to the diet. When
the breadth of trophic niches was compared, overlap ranged from 0.83 (weight categories)
to one (main food categories). As these leopard species have approximately
the same size and comparable food habits, one can predict that competition will arise
when they live in sympatry. On mountains, climate change has been elevating the
upper forest limit, where both leopard species occur. This means a habitat increase
for common leopards and a substantial habitat reduction for snow leopards, whose
range is going to be squeezed between the forest and the barren rocky altitudes, with
medium- to long-term undesirable effects on the conservation of this endangered cat
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Maheshwari, A., Midha, N., Chehrukupalli, A. (2014). Participatory Rural Appraisal and Compensation Intervention: Challenges and Protocols While Managing Large Carnivore–Human Conflict. Human Dimensions of Wildlife: An International Journal, 19, 62–71.
Abstract: When large carnivores cause socioeconomic losses in a community, conflict increases,
retaliatory killing of the carnivore can occur, and conservation efforts are undermined.
We focused on Participatory Rural Appraisal (PRA) and economic compensation
schemes as approaches for managing conflict. PRA is a tool for collecting data on
the large carnivore–human conflict and economic compensation schemes for those
affected negatively by carnivore presence. We reviewed published papers and reports
on large carnivore–human conflicts, PRA, and compensation schemes. This article
details insights into common pitfalls, key lessons learned, possible solutions including
new approaches for compensation and protocols to be followed while managing large
carnivore–human conflict. We hope to contribute to a meaningful dialogue between
locals, managers, and researchers and help in effective implementation of conservation
programs to mitigate large carnivore–human conflict around the protected areas.
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Bischof, R., Hameed, S., Ali, H., Kabir, M., Younas, M., Shah, K. A., Din, J. U., Nawaz, M. A. (2013). Using time-to-event analysis to complement hierarchical methods when assessing determinants of photographic detectability during camera trapping. Methods in Ecology and Evolution, .
Abstract: 1. Camera trapping, paired with analytical methods for estimating occupancy, abundance and other ecological parameters, can yield information with direct consequences for wildlife management and conservation. Although ecological information is the primary target of most camera trap studies, detectability influences every aspect from design to interpretation.
2. Concepts and methods of time-toevent analysis are directly applicable to camera trapping, yet this statistical field has thus far been ignored as a way to analyze photographic capture data. to illustrate the use to time-to-event statistics and to better understand how photographic evidence accumulates, we explored patterns in tow related measure of detectability: Detection probability and time to detection. We analyzed camera trap data for three sympatric carnivores ( snow Leopard, red fox and stone marten) in the mountains of northern Pakistan and tested predictions about patterns in detectability across species, sites and time.
3. We found species-specific differences in the magnitude of detectability and the factors influencing it, reinforcing the need to consider determinants of detectability in study design and to account for them during analysis. Photographic detectability of snow leopard was noticeably lower than that of red fox, but comparable to detectability of stone marten. Site-specific attributes such as the presence of carnivore sign ( snow Leopard), terrain ( snow leopard and red fox) and application for lures ( red fox) influenced detectability. For the most part, detection probability was constant over time.
4. Species- specific differences in factors determining detectability make camera trap studies targeting multiple species particularly vulnerable to misinterpretation if the hierarchical origin of the data is ignored. Investigators should consider not only the magnitude of detectability, but also the shape of the curve describing the cumulative process of photographic detection, as this has consequences for both determining survey effort and the election of analytical models. Weighted time-to -event analysis can complement occupancy analysis and other hierarchal methods by providing additional tools for exploring camera trap data and testing hypotheses regarding the temporal aspect of photographic evidence accumulation.
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Lyngdoh, S., Shrotriya, S., Goyal, S. P., Clements, H., Hayward, M. W., Habib, B. (2014). Prey Preferences of the Snow Leopard (Panthera uncia): Regional Diet Specificity Holds Global Significance for Conservation. Plos One, 9(2), 1–11.
Abstract: The endangered snow leopard is a large felid that is distributed over 1.83 million km2 globally. Throughout its range it relies on a limited number of prey species in some of the most inhospitable landscapes on the planet where high rates of human persecution exist for both predator and prey. We reviewed 14 published and 11 unpublished studies pertaining to snow leopard diet throughout its range. We calculated prey consumption in terms of frequency of occurrence and biomass consumed based on 1696 analysed scats from throughout the snow leopard’s range. Prey biomass consumed was calculated based on the Ackerman’s linear correction factor. We identified four distinct physiographic and snow leopard prey type zones, using cluster analysis that had unique prey assemblages and had key prey characteristics which supported snow leopard occurrence there. Levin’s index showed the snow leopard had a specialized dietary niche breadth. The main prey of the snow leopard were Siberian ibex (Capra sibrica), blue sheep (Pseudois nayaur), Himalayan tahr (Hemitragus jemlahicus), argali (Ovis ammon) and marmots (Marmota spp). The significantly preferred prey species of snow leopard weighed 5565 kg, while the preferred prey weight range of snow leopard was 36–76 kg with a significant preference for Siberian ibex and blue sheep. Our meta-analysis identified critical dietary resources for snow leopards throughout their distribution and illustrates the importance of understanding regional variation in species ecology; particularly prey species
that have global implications for conservation.
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Ale, S., Shrestha, B., and Jackson, R. (2014). On the status of Snow Leopard Panthera Uncia (Schreber 1775) in Annapurna, Nepal. Journal of Threatened Taxa, (6(3)), 5534–5543.
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Ferretti, F., Lovari, S., Minder, I., Pellizzi, B. (2014). Recovery of the snow leopard in Sagarmatha (Mt.Everest) National Park: effects on main prey. European Journal of Wildlife Research, (60), 559–562.
Abstract: Consequences of predation may be particularly
heavy on small populations of herbivores, especially if they
are threatened with extinction. Over the 2006–2010 period, we
documented the effects of the spontaneous return of the endangered
snow leopard on the population of the vulnerable
Himalayan tahr. The study area was an area of central
Himalaya where this cat disappeared c. 40 years before, because
of persecution by man. Snow leopards occurred mainly
in areas close to the core area of tahr distribution. Tahr was the
staple (56.3 %) of snow leopards. After the arrival of this cat,
tahr decreased by more than 2/3 from 2003 to 2010 (mainly
through predation on kids). Subsequently, the density of snow
leopards decreased by 60%from2007 to 2010. The main prey
of snow leopards in Asia (bharal, marmots) were absent in our
study area, forcing snow leopards to specialize on tahr. The
restoration of a complete prey spectrum should be favoured
through reintroductions, to conserve large carnivores and to
reduce exploitation of small populations of herbivores, especially
if threatened.
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