|
Vogt, P. (1982). New enclosures for snow leopards (Uncia uncia) at Krefeld Zoo. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 67–70). Helsinki: Helsinki Zoo.
|
|
|
Wahlberg, C. (1980). Autopsy findings and causes of death in captive snow leopards (Panthera uncia): a preliminary report. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 205–217). Helsinki: Helsinki Zoo.
|
|
|
Wahlberg, C., & Tarkkanen, A. (1980). On the multiple ocular coloboma with retinal dysplasia (MOC) in snow leopards, Pantera uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 183–194). Helsinki: Helsinki Zoo.
|
|
|
Wahlberg, C., Tarkkanen, A., & Blomqvist, L. (1982). Further observations on the multiple ocular coloboma (MOC) in the snow leopard, Panthers uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 3, pp. 139–144). Helsinki: Helsinki Zoo.
Abstract: The first observation of the occurrence of multiple ocular coloboma (MOC) in a snow leopard was reported in the International Pedigree Book of Snow Leopards Volume I in 1978 (1). The lesions in this syndrome consist of coloboma of the upper eye lid and uveal coloboma of the globe. Even colobomatous retinal cysts and retinal dysplasia have been noted. The ethiology of in all ten cases of MOC in the snow leopards kept at the Helsinki Zoo were described and discussed in detail in Volume II of the International Pedigree Book of Snow Leopards (2,3). Three cases of MOC in the snow leopards kept at Henry Doorly Zoo, Omaha, Ne., have been described by Phillips (4), one case is known of in Amsterdam (van Bree, personal communication), and two cases in Zoo Zurich (Isenbugel and Weilenmann, pers. comm.) The ethiology of the defect is still not known although various theories ranging from genetic to exogenous factors have been presented.
|
|
|
Waits, L. P., Buckley-Beason, V. A., Johnson, W. E., Onorato, D., & McCarthy, T. (2006). A select panel of polymorphic microsatellite loci for individual identification of snow leopards (Panthera uncia)
(Vol. 7).
Abstract: Snow leopards (Panthera uncia) are elusive endangered carnivores found in remote mountain regions of Central Asia. New methods for identifying and counting snow leopards are needed for conservation and management efforts. To develop molecular genetic tools for individual identification of hair and faecal samples, we screened 50 microsatellite loci developed for the domestic cat (Felis catus) in 19 captive snow leopards. Forty-eight loci were polymorphic with numbers of alleles per locus ranging from two to 11. The probability of observing matching genotypes for unrelated individuals (2.1 x10-11) and siblings (7.5x10-5) using the 10 most polymorphic loci was low, suggesting that this panel would easily discriminate among individuals in the wild.
|
|
|
Wegge, P., Shrestha, R., Flagstad, O. (2012). Snow leopard Panthera uncia predation on livestock and wild prey in a mountain valley in northern Nepal: implications for conservation management. Wildlife Biology, 18(10.2981/11-049), 131–141.
Abstract: The globally endangered snow leopard Panthera uncia is sparsely distributed throughout the rugged mountains in Asia.
Its habit of preying on livestock poses a main challenge to management. In the remote Phu valley in northern Nepal, we
obtained reliable information on livestock losses and estimated predator abundance and diet composition from DNA
analysis and prey remains in scats. The annual diet consisted of 42%livestock. Among the wild prey, bharal (blue sheep/
naur) Pseudois nayaur was by far the most common species (92%). Two independent abundance estimates suggested that
there were six snow leopards in the valley during the course of our study. On average, each snow leopard killed about one
livestock individual and two bharal permonth. Predation loss of livestock estimated fromprey remains in scats was 3.9%,
which was in concordance with village records (4.0%). From a total count of bharal, the only large natural prey in the area
and occurring at a density of 8.4 animals/km2 or about half the density of livestock, snow leopards were estimated to
harvest 15.1% of the population annually. This predation rate approaches the natural, inherent recruitment rate of this
species; in Phu the proportion of kids was estimated at 18.4%. High livestock losses have created a hostile attitude against
the snow leopard and mitigation measures are needed. Among innovative management schemes now being implemented
throughout the species’ range, compensation and insurance programmes coupled with other incentive measures are
encouraged, rather than measures to reduce the snow leopard’s access to livestock. In areas like the Phu valley, where the
natural prey base consists mainly of one ungulate species that is already heavily preyed upon, the latter approach, if
implemented, will lead to increased predation on this prey, which over time may suppress numbers of both prey and
predator.
Keywords: bharal, blue sheep, diet, genetic sampling, naur, Panthera uncia, predation, Pseudois nayaur, scat analysis, snow leopard, wildlife conflict
|
|
|
Wei, L., Wu, X., & Jiang, Z. (2008). The complete mitochondrial genome structure of snow leopard Panthera uncia.
Abstract: The complete mitochondrial genome (mtDNA) of snow leopard Panthera uncia was obtained by using the polymerase chain reaction (PCR) technique based on the PCR fragments of 30 primers we designed. The entire mtDNA sequence was 16 773 base pairs (bp) in length, and the base composition was: A-5,357ª“,Ž+bp (31.9%); C-4,444ª”,Ž+bp (26.5%); G-2,428ª“,Ž+bp (14.5%); T-4,544ª”,Ž+bp (27.1%). The structural characteristics [0] of the P. uncia mitochondrial genome were highly similar to these of Felis catus, Acinonyx jubatus, Neofelis nebulosa and other mammals. However, we found several distinctive features of the mitochondrial genome of Panthera unica. First, the termination codon of COIII was TAA, which differed from those of F. catus, A. jubatus and N. nebulosa. Second, tRNASer (AGY), which lacked the ''DHU'' arm, could not be folded into the typical cloverleaf-shaped structure. Third, in the control region, a long repetitive sequence in RS-2 (32ª“,Ž+bp) region was found with 2 repeats while one short repetitive segment (9ª”,Ž+bp) was found with 15 repeats in the RS-3 region. We performed phylogenetic analysis based on a 3 816ª",Ž+bp concatenated sequence of 12S rRNA, 16S rRNA, ND2, ND4, ND5, Cyt b and ATP8 for P. uncia and other related species, the result indicated that P. uncia and P. leo were the sister species, which was different from the previous findings. (c) 2008 Springer Science+Business Media B.V.
|
|
|
Weiskopf, S. R., Kachel, S. M., McCarthy, K. P. (2016). What Are Snow Leopards Really Eating? Identifying Bias in Food-Habit Studies. Wildlife Society Bulletin, , 1–8.
Abstract: Declining prey populations are widely recognized as a primary threat to snow leopard (Panthera
uncia) populations throughout their range. Effective snow leopard conservation will depend upon reliable
knowledge of food habits. Unfortunately, past food-habit studies may be biased by inclusion of nontarget
species in fecal analysis, potentially misinforming managers about snow leopard prey requirements.
Differentiation between snow leopard and sympatric carnivore scat is now cost-effective and reliable using
genetics. We used fecal mitochondrial DNA sequencing to identify scat depositors and assessment bias in
snow leopard food-habit studies. We compared presumed, via field identification, and genetically confirmed
snow leopard scats collected during 2005 and 2012 from 4 sites in Central Asia, using standard forensic
microscopy to identify prey species. Field identification success varied across study sites, ranging from 21% to
64% genetically confirmed snow leopard scats. Our results confirm the importance of large ungulate prey for
snow leopards. Studies that fail to account for potentially commonplace misidentification of snow leopard
scat may mistakenly include a large percentage of scats originating from other carnivores and report
inaccurate dietary assessments. Relying on field identification of scats led to overestimation of percent
occurrence, biomass, and number of small mammals consumed, but underestimated values of these measures for large ungulates in snow leopard diet. This clarification suggests that the conservation value of secondary prey, such as marmots (Marmota spp.) and other small mammals, may be overstated in the literature; stable snow leopard populations are perhaps more reliant upon large ungulate prey than previously understood.
|
|
|
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.
|
|
|
Xiao, C., Bai, D., Lambert, J. P., Li, Y., Cering, L., Gong, Z., Riordan, P., Shi, K. (2022). How Snow Leopards Share the Same Landscape with Tibetan Agro-pastoral Communities in the Chinese Himalayas. Journal of Resources and Ecology, 13(3), 483–500.
Abstract: The snow leopard (Panthera uncia) inhabits a human-altered alpine landscape and is often tolerated by residents in regions where the dominant religion is Tibetan Buddhism, including in Qomolangma NNR on the northern side of the Chinese Himalayas. Despite these positive attitudes, many decades of rapid economic development and population growth can cause increasing disturbance to the snow leopards, altering their habitat use patterns and ultimately impacting their conservation. We adopted a dynamic landscape ecology perspective and used multi-scale technique and occupancy model to better understand snow leopard habitat use and coexistence with humans in an 825 km2 communal landscape. We ranked eight hypothetical models containing potential natural and anthropogenic drivers of habitat use and compared them between summer and winter seasons within a year. HABITAT was the optimal model in winter, whereas ANTHROPOGENIC INFLUENCE was the top ranking in summer (AICcw≤2). Overall, model performance was better in the winter than in the summer, suggesting that perhaps some latent summer covariates were not measured. Among the individual variables, terrain ruggedness strongly affected snow leopard habitat use in the winter, but not in the summer. Univariate modeling suggested snow leopards prefer to use rugged land in winter with a broad scale (4000 m focal radius) but with a lesser scale in summer (30 m); Snow leopards preferred habitat with a slope of 22° at a scale of 1000 m throughout both seasons, which is possibly correlated with prey occurrence. Furthermore, all covariates mentioned above showed inextricable ties with human activities (presence of settlements and grazing intensity). Our findings show that multiple sources of anthropogenic activity have complex connections with snow leopard habitat use, even under low human density when anthropogenic activities are sparsely distributed across a vast landscape. This study is also valuable for habitat use research in the future, especially regarding covariate selection for finite sample sizes in inaccessible terrain.
|
|