| Home | << 1 2 3 4 5 6 7 8 9 10 >> [11–20] |
|
Peden, W. M., Richard, J. L., Trampel, D. W., & Brannian, R. E. (1985). Mycotic pneumonia and meningoencephalitis due to Aspergillus terreus in a neonatal snow leopard (Panthera uncia) (Vol. 21).
Abstract: On 14 May 1983, two female snow leopard (Panthera uncia) cubs were born in the Kansas City Zoological Gardens to a primiparous female. The female showed little interest in the cubs, one of which had a body temperature of 30 C, so they were removed for hand-rearing. On 15 May, one cub was less active, and did not nurse as well as its littermate.
Keywords: Aspergillus; hand rearing; Meningoencephalitis; panthera uncia; Pneumonia; snow leopard; zoological
|
|
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. |
|
Shrestha, A., Thapa, K., Subba, S. A., Dhakal, M., Devkota, B. P., Thapa, G. J., Shrestha, S., Malla, S., Thapa, K. (2019). Cats, canines, and coexistence: dietary differentiation between the sympatric Snow Leopard and Grey Wolf in the western landscape of Nepal Himalaya. Journal of Threatened Taxa, 11(7), 13815–13821.
Abstract: Understanding the dietary habits of sympatric apex carnivores advances our knowledge of ecological processes and aids their conservation. We compared the diets of the sympatric Snow Leopard Panthera uncia and Grey Wolf Canis lupus using standard micro-histological analyses of scats collected from the western complex of Nepal Himalaya. Our study revealed one of the highest recorded contributions of livestock to the diet of top predators (55% for Grey Wolf and 39% for Snow Leopard) and high dietary overlap (0.82) indicating potential exploitative or interference competition. Their diet composition, however, varied significantly based on their consumption of wild and domestic prey. Limitation in data precludes predicting direction and outcome of inter-specific interactions between these predators. Our findings suggest a high rate of negative interaction with humans in the region and plausibly retaliatory killings of these imperilled predators. To ensure the sustained survival of these two apex carnivores, conservation measures should enhance populations of their wild prey species while reducing livestock losses of the local community through preventive and mitigative interventions.
|
|
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.
Keywords: habitat use; landscape ecology; occupancy model; Qomolangma; Panthera uncia
|
|
Changxi, X., 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.
Keywords: habitat use; landscape ecology; occupancy model; Qomolangma; Panthera uncia
|
|
Oli, M. (1994). Snow leopards and blue sheep in Nepal: Densities and predator: Prey ratio (Vol. 75).
Abstract: I studied snow leopards (Panthera uncia) and blue sheep (Pseudois nayaur) in Manang District, Annapurna Conservation Area, Nepal, to estimate numbers and analyze predatorprey interactions. Five to seven adult leopards used the 105-km2 study area, a density of 4.8 to 6.7 leopards/100 km2. Density of blue sheep was 6.6-10.2 sheep/km2, and biomass density was 304 kg/km2. Estimated relative biomass consumed by snow leopards suggested that blue sheep were the most important prey; marmots (Marmota himalayana) also contributed significantly to the diet of snow leopards. Snow leopards in Manang were estimated to harvest 9-20% of total biomass and 11-24% of total number of blue sheep annually. Snow leopard :blue sheep ratio was 1 :1 14-1 :159 on a weight basis, which was considered sustainable given the importance of small mammals in the leopard's diet and the absence of other competing predators.
|
|
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.
|
|
Ming, M., Munkhtsog, B., McCarthy, T., McCarthy, K. (2011). Monitor ing of Population Density of Snow Leopard in X injiang. Journal of Ecology and Rural Environment, 27(1), 79–83.
Abstract: The snow leopard (Uncia uncia) is a very rare species in China. The survey of traces of snow leopard in Kunlun, Altay and Tianshan is them a instep of the Project of Snow Leopard in X injiang supported by the International Snow Leopard Trust ( SLT) and the Xinjiang Conservation Fund (XCF). During the field survey from 2004 to 2010, the Xinjiang Snow Leopard Group ( XSLG) spent about 270 days in over 20 different places, covering over 150 transects totaling nearly 190 km, and found 1- 3 traces per kilometer. The traces of snow leopard recorded include dung, odor, chains of footprints, scraping, paw nail marks, lying mark, fur, urine, bloodstain, leftover of prey corpse, roaring and others. Based on tracer image analyses, the XSLG got to know primarily scopes of the domains, distribution and relative density of the snow leopard in these areas. Then the group began to take infrared photos, conducted survey of food sources of the leopards, investigated fur market and paths of trading, and cases of killing, and carry out civil survey through questionnaire, non government organization community service and research on conflicts between grazing and wild life protection. A total of 36 infrared came ras were laid out, working a total of about 2 094 days or 50 256 hours. A total 71 rolls of film were collected and developed, includ ing 32 clear pictures of snow leopards, thus making up a shooting rate or capture rate of 1.53%. It was ascertained that in Tomur Peak area, there were 5- 8 snow leopards roaming within a range of 250 km2, forming a population density of 2��0- 3��2 per 100 km2. After compar ing the various monitoring results, the advantages and limitations of different monitoring methods have been discussed.
Keywords: Uncia uncia; snow leopard; monitoring method; trace; infrared camera; relative intensity
|
|
Janovsky, M., Grone, A., Ciardo, D., Vollm, J., Burnens, A., Fatzer, R., et al. (2006). Phaeohyphomycosis in a Snow Leopard (Uncia uncia) due to Cladophialophora bantiana (Vol. 134).
Abstract: Phaeohyphomycosis caused by Cladophialophora bantiana was diagnosed in a 5-month-old snow leopard with spastic paralysis of the hind legs and inability to defaecate or urinate. At post-mortem examination, a greenish soft mass resembling an abscess was found on one side of the epidural space at the fourth lumbar vertebral body. Histological examination revealed a purulent meningitis with myelomalacia. Dematiaceous fungal hyphae, present within the inflammatory infiltrate, were identified as C. bantiana by culture and sequence analysis of the 18S ribosomal RNA gene. This neurotropic fungus rarely affects organs other than the brain in human beings and cats, and has been reported only occasionally in Europe. The case described suggests that phaeohyphomycosis due to C. bantiana infection may be recognized more frequently in the future and the possible involvement of organs other than the brain should be borne in mind.
|
|
Suryawanshi, K. R., Bhatnagar, Y. V. B., Redpath, S., Mishra, C. (2013). People, predators and perceptions: patterns of livestock depredation by snow leopards and wolves. Journal of Applied Ecology, 50, 550–560.
Abstract: 1. Livestock depredation by large carnivores is an important conservation and economic concern
and conservation management would benefit from a better understanding of spatial variation and underlying causes of depredation events. Focusing on the endangered snow leopard Panthera uncia and the wolf Canis lupus, we identify the ecological factors that predispose areas within a landscape to livestock depredation. We also examine the potential mismatch between reality and human perceptions of livestock depredation by these carnivores whose survival is threatened due to persecution by pastoralists. 2. We assessed the distribution of the snow leopard, wolf and wild ungulate prey through field surveys in the 4000 km2 Upper Spiti Landscape of trans-Himalayan India. We interviewed local people in all 25 villages to assess the distribution of livestock and peoples’ perceptions of the risk to livestock from these carnivores. We monitored village-level livestock mortality over a 2-year period to assess the actual level of livestock depredation. We quantified several possibly influential independent variables that together captured variation in topography, carnivore abundance and abundance and other attributes of livestock. We identified the key variables influencing livestock depredation using multiple logistic regressions and hierarchical partitioning. 3. Our results revealed notable differences in livestock selectivity and ecological correlates of livestock depredation – both perceived and actual – by snow leopards and wolves. Stocking density of large-bodied free-ranging livestock (yaks and horses) best explained people’s threat perception of livestock depredation by snow leopards, while actual livestock depredation was explained by the relative abundance of snow leopards and wild prey. In the case of wolves, peoples’ perception was best explained by abundance of wolves, while actual depredation by wolves was explained by habitat structure. 4. Synthesis and applications. Our results show that (i) human perceptions can be at odds with actual patterns of livestock depredation, (ii) increases in wild prey populations will intensify livestock depredation by snow leopards, and prey recovery programmes must be accompanied by measures to protect livestock, (iii) compensation or insurance programmes should target large-bodied livestock in snow leopard habitats and (iv) sustained awareness programmes are much needed, especially for the wolf. |