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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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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
Keywords: lion; clouded-leopard; cheetah; tiger; leopard; snow-leopard; India; Panthera-leo; Neofelis-nebylosa; Acinonyx-jubatus; Panthera-tigris; Panthera-pardus; Panthera-uncia; behavior; ecology; snow leopard; browse; panthera; uncia; pardus; clouded; leo; neofelis; nebylosa; ancinonyx; jubatus; 820
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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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Hussain, S. (2003). The status of the snow leopard in Pakistan and its conflict with local farmers (Vol. 37).
Abstract: Between 1998 and 2001 I carried out surveys in four areas in the Baltistan district of the Northern Areas of Pakistan to estimate the population of the snow leopard and to examine the threats to its future conservation. I estimate that a total of 36-50 snow leopards are present in the areas surveyed. Based on the availability of suitable snow leopard habitat and of its prey species, I estimate that 90-120 snow leopards are potentially present in Baltistan and 300-420 throughout its range within Pakistan's borders. Although this estimate is higher than extrapolations based on earlier surveys, the long-term future of the snow leopard is under threat. This is mainly due to retaliatory killings by farmers, and poaching for pelts and other body parts. Species-focused conservation policies, particularly those targeting ungulates for the promotion of trophy hunting, may constitute an additional threat to snow leopard conservation in the region. However, all forms of threats to the snow leopard in Baltistan appear to emanate from the relatively poor economic conditions of the local people.
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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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McCarthy, T. (2000). Ecology and Conservation of Snow Leopards, Gobi Brown Bears, and Wild Bactrian Camels in Mongolia. Ph.D. thesis, University of Massachusetts, Amherst, .
Abstract: Snow leopard ecology, distribution and abundance in Mongolia were studied between 1993 and 1999. I placed VHF and satellite radio-collars on 4 snow leopards, 2 males and 2 females, to determine home ranges, habitat use, movements, and activity. Home ranges of snow leopards in Mongolia were substantially larger than reported elsewhere. Males ranged over 61 – 142 km2 and female 58 to 1,590 km2. Cats had crepuscular activity patterns with daily movements averaging 5.1 km. Intraspecific distances averaged 1.3 km for males to 7.8 km for males. Leopards selected moderately to very-broken habitat with slopes > 20o, in areas containing ibex. Leopard distribution and abundance was determined using sign surveys. Leopard range in Mongolia is approximately 103,000 km2 but cats are not uniformly distributed within that range. High-density areas include the eastern and central Transaltai Gobi and the northern Altai ranges. Relative leopard densities compared well with relative ibex densities on a regional basis. A snow leopard conservation plan was drafted for Mongolia that identifies problems and threats, and provides an action plan. Wild Bactrian camels occur in the Great Gobi National Park (GGNP) and are thought to be declining due to low recruitment. I surveyed camels by jeep and at oases, observing 142 (4.2% young) and 183 (5.3% young) in 1997 and 1998. Current range was estimated at 33,300 km2. Some winter and calving ranges were recently abandoned. Track sizes and tooth ages from skulls were used to assess demographics. A deterministic model was produced that predicts camel extinction within 25 to 50 years under current recruitment rates and population estimates. Gobi brown bears are endemic to Mongolia and may number less than 35. Three population isolates may occur. I collected genetic material from bears at oases using hair traps. Microsatellite analyses of nuclear DNA determined sixteen unique genotypes, only two of which occurred at more than one oases. Genetic diversity was very low with expected heterozygosity = 0.32, and alleles per locus = 2.3. Mitochondrial DNA sequences were compared to other clades of brown bear and found to fall outside of all known lineages.
Keywords: snow leopard; Uncia uncia; Mongolia; radio-collar; habitat use; movements; ecology; wild camel; brown bear; 5340
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