Korablev, M. P., Poyarkov, A. D., Karnaukhov, A. S., Zvychaynaya, E. Y., Kuksin, A. N., Malykh, S. V., Istomov, S. V., Spitsyn, S. V., Aleksandrov, D. Y., Hernandez-Blanco, J. A., Munkhtsog, B., Munkhtogtokh, O., Putintsev, N. I., Vereshchagin, A. S., Becmurody, A., Afzunov, S., Rozhnov, V. V. (2021). Large-scale and fine-grain population structure and genetic diversity of snow leopards (Panthera uncia Schreber, 1776) from the northern and western parts of the range with an emphasis on the Russian population. Conservation Genetics, .
Abstract: The snow leopard (Panthera uncia Schreber, 1776) population in Russia and Mongolia is situated at the northern edge of the range, where instability of ecological conditions and of prey availability may serve as prerequisites for demographic instability and, consequently, for reducing the genetic diversity. Moreover, this northern area of the species distribution is connected with the western and central parts by only a few small fragments of potential habitats in the Tian-Shan spurs in China and Kazakhstan. Given this structure of the range, the restriction of gene flow between the northern and other regions of snow leopard distribution can be expected. Under these conditions, data on population genetics would be extremely important for assessment of genetic diversity, population structure and gene flow both at regional and large-scale level. To investigate large-scale and fine-grain population structure and levels of genetic diversity we analyzed 108 snow leopards identified from noninvasively collected scat samples from Russia and Mongolia (the northern part of the range) as well as from Kyrgyzstan and Tajikistan (the western part of the range) using panel of eight polymorphic microsatellites. We found low to moderate levels of genetic diversity in the studied populations. Among local habitats, the highest heterozygosity and allelic richness were recorded in Kyrgyzstan (He = 0.66 ± 0.03, Ho = 0.70 ± 0.04, Ar = 3.17) whereas the lowest diversity was found in a periphery subpopulation in Buryatia Republic of Russia (He = 0.41 ± 0.12, Ho = 0.29 ± 0.05, Ar = 2.33). In general, snow leopards from the western range exhibit greater genetic diversity (He = 0.68 ± 0.04, Ho = 0.66 ± 0.03, Ar = 4.95) compared to those from the northern range (He = 0.60 ± 0.06, Ho = 0.49 ± 0.02, Ar = 4.45). In addition, we have identified signs of fragmentation in the northern habitat, which have led to significant genetic divergence between subpopulations in Russia. Multiple analyses of genetic structure support considerable genetic differentiation between the northern and western range parts, which may testify to subspecies subdivision of snow leopards from these regions. The observed patterns of genetic structure are evidence for delineation of several management units within the studied populations, requiring individual approaches for conservation initiatives, particularly related to translocation events. The causes for the revealed patterns of genetic structure and levels of genetic diversity are discussed.
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Koju. N. P,, Bashyal, B., Pandey, B. P., Shah, S. N., Thami, S., Bleisch, W. V. (2020). First camera-trap record of the snow leopard Panthera uncia in Gaurishankar Conservation Area, Nepal. Oryx, , 1–4.
Abstract: The snow leopard Panthera uncia is the flagship species of the high mountains of the Himalayas. There is po- tentially continuous habitat for the snow leopard along the northern border of Nepal, but there is a gap in information about the snow leopard in Gaurishankar Conservation Area. Previous spatial analysis has suggested that the Lamabagar area in this Conservation Area could serve as a transbound- ary corridor for snow leopards, and that the area may con- nect local populations, creating a metapopulation. However, there has been no visual confirmation of the species in Lamabagar. We set !! infrared camera traps for " months in Lapchi Village of Gaurishankar Conservation Area, where blue sheep Pseudois nayaur, musk deer Moschus leucogaster and Himalayan tahr Hemitragus jemlahicus, all snow leopard prey species, had been observed. In November #$!% at &,!$$ m, ' km south-west of Lapchi Village, one camera recorded three images of a snow leopard, the first photographic evidence of the species in the Conservation Area. Sixteen other species of mammals were also recorded. Camera-trap records and sightings indicated a high abun- dance of Himalayan tahr, blue sheep and musk deer. Lapchi Village may be a potentially important corridor for snow leopard movement between the east and west of Nepal and northwards to Quomolongma National Park in China. However, plans for development in the region present in- creasing threats to this corridor. We recommend develop- ment of a transboundary conservation strategy for snow leopard conservation in this region, with participation of Nepal, China and international agencies.
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Atzeni, L., Cushman, S. A., Bai, D., Wang, J., Chen, P., Shi,
K., Riordan, P. (2020). Meta-replication, sampling bias, and multi-scale model selection:
A case study on snow leopard (Panthera uncia) in western China. Ecology and Evolution, , 1–27.
Abstract: Replicated multiple scale species distribution models (SDMs)
have become increasingly important to identify the correct variables
determining species distribution and their influences on ecological
responses. This study explores multi-scale habitat relationships of the
snow leopard (Panthera uncia) in two study areas on the Qinghai–Tibetan
Plateau of western China. Our primary objectives were to evaluate the
degree to which snow leopard habitat relationships, expressed by
predictors, scales of response, and magnitude of effects, were
consistent across study areas or locally landcape-specific. We coupled
univariate scale optimization and the maximum entropy algorithm to
produce multivariate SDMs, inferring the relative suitability for the
species by ensembling top performing models. We optimized the SDMs based
on average omission rate across the top models and ensembles’ overlap
with a simulated reference model. Comparison of SDMs in the two study
areas highlighted landscape-specific responses to limiting factors.
These were dependent on the effects of the hydrological network,
anthropogenic features, topographic complexity, and the heterogeneity of
the landcover patch mosaic. Overall, even accounting for specific local
differences, we found general landscape attributes associated with snow
leopard ecological requirements, consisting of a positive association
with uplands and ridges, aggregated low-contrast landscapes, and large
extents of grassy and herbaceous vegetation. As a means to evaluate the
performance of two bias correction methods, we explored their effects on
three datasets showing a range of bias intensities. The performance of
corrections depends on the bias intensity; however, density kernels
offered a reliable correction strategy under all circumstances. This
study reveals the multi-scale response of snow leopards to environmental
attributes and confirms the role of meta-replicated study designs for
the identification of spatially varying limiting factors. Furthermore,
this study makes important contributions to the ongoing discussion about
the best approaches for sampling bias correction.
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Chetri, M., Odden, M., Devineau, O., McCarthy, T., Wegge, P. (2020). Multiple factors influence local perceptions of snow leopards and
Himalayan wolves in the central Himalayas, Nepal. PeerJ, , 1–18.
Abstract: An understanding of local perceptions of carnivores is
important for conservation and management planning. In the central
Himalayas, Nepal, we interviewed 428 individuals from 85 settlements
using a semi-structured questionnaire to quantitatively assess local
perceptions and tolerance of snow leopards and wolves. We used
generalized linear mixed effect models to assess influential factors,
and found that tolerance of snow leopards was much higher than of
wolves. Interestingly, having experienced livestock losses had a minor
impact on perceptions of the carnivores. Occupation of the respondents
had a strong effect on perceptions of snow leopards but not of wolves.
Literacy and age had weak impacts on snow leopard perceptions, but the
interaction among these terms showed a marked effect, that is, being
illiterate had a more marked negative impact among older respondents.
Among the various factors affecting perceptions of wolves, numbers of
livestock owned and gender were the most important predictors. People
with larger livestock herds were more negative towards wolves. In terms
of gender, males were more positive to wolves than females, but no such
pattern was observed for snow leopards. People’s negative perceptions
towards wolves were also related to the remoteness of the villages.
Factors affecting people’s perceptions could not be generalized for the
two species, and thus need to be addressed separately. We suggest future
conservation projects and programs should prioritize remote settlements.
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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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Ale, S. B., Yonzon, P., & Thapa, K. (2007). Recovery of snow leopard Uncia uncia in Sagarmatha (Mount Everest) National Park, Nepal (Vol. 41).
Abstract: From September to November 2004 we conducted surveys of snow leopard Uncia uncia signs in three major valleys in Sagarmatha (Mount Everest) National Park in Nepal using the Snow Leopard Information Management System, a standardized survey technique for snow leopard research. We walked 24 transects covering c. 14 km and located 33 sites with 56 snow leopard signs, and 17 signs incidentally in other areas. Snow leopards appear to have re-inhabited the Park, following their disappearance c. 40 years ago, apparently following the recovery of Himalayan tahr Hemitragus jemlahicus and musk deer Moschus chrysogaster populations. Taken together the locations of all 73 recent snow leopard signs indicate that the species is using predominantly grazing land and shrubland/ open forest at elevations of 3,000-5,000 m, habitat types that are also used by domestic and wild ungulates. Sagarmatha is the homeland of c. 3,500 Buddhist Sherpas with .3,000 livestock. Along with tourism and associated developments in Sagarmatha, traditional land use practices could be used to ensure coexistence of livestock and wildlife, including the recovering snow leopards, and ensure the wellbeing of the Sherpas.
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Ali, S. M. (1990). The Cats of India. Myforest, 26(3), 275–291.
Abstract: Describes the range, behaviour and ecology of lion Panthera leo, tiger P. tigris, leopard P. pardus, snow leopard P. uncia, clouded leopard Neofelis nebylosa and cheetah Acinonyx jubatus. -P.J.Jarvis
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Blomqvist, L., & Nystrom, V. (1980). On identifying snow leopards, Panthera uncia, by their facial markings. International Pedigree Book of Snow Leopards, , 159–167.
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Blomqvist, L. (1982). The 1981 annual report of the captive snow leopards (Panthera uncia) population. International Pedigree Book of Snow Leopards, 3.
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Blomqvist, L. (2008). International Pedigree Book for Snow Leopards, Uncia uncia. Helsinki: Helsinki Zoo.
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