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Stidworthy, M. F., Lewis, J. C. M., Penderis, J., & Palmer, A. C. (2009). Progressive encephalomyelopathy and cerebellar degeneration in a captive-bred snow leopard (Uncia uncia) (Vol. 162).
Abstract: PROGRESSIVE encephalomyelopathy with cerebellar degeneration has been described in captive cheetahs (Palmer and others 2001) and in young domestic cats (Palmer and Cavanagh 1995). This case report describes the clinical and histopathological findings in a very similar condition affecting a young snow leopard (Uncia uncia) that had been born in a zoological park in eastern England as part of the globally coordinated breeding programme for this critically endangered species.
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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.
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McCarthy, T., Fuller, T., & Munkhtsog, B. (2005). Movements and activities of snow leopards in Southwestern Mongolia (Vol. 124).
Abstract: Four adult (2M:2F) snow leopards (Uncia uncia) were radio-monitored (VHF; one also via satellite) year-round during 1994-1997 in the Altai Mountains of southwestern Mongolia where prey densities (i.e., ibex, Capra siberica) were relatively low (0.9/km2). Marked animals were more active at night (51%) than during the day (35%). Within the study area, marked leopards showed strong a.nity for steep and rugged terrain, high use of areas rich in ungulate prey, and a.nity for habitat edges. The satellite-monitored leopard moved more than 12 km on 14% of consecutive days monitored. Home ranges determined by standard telemetry techniques overlapped substantially and were at least 13-141 km2in size. However, the satellite-monitored individual apparently ranged over an area of at least 1590 km2, and perhaps over as much as 4500 km2. Since telemetry attempts from the ground were
frequently unsuccessful dx¬ 72%_, we suspect all marked animals likely had large home ranges. Relatively low prey abundance in the area also suggested that home ranges of >500 km2were not unreasonable to expect, though these are >10-fold larger than measured in any other part of snow leopard range. Home ranges of snow leopards may be larger than we suspect in many areas, and thus estimation of snow leopard conservation status must rigorously consider logistical constraints inherent in telemetry studies, and the relative abundance of prey.
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Kalashnikova, Y. A., Karnaukhov, A. S., Dubinin, M. Y., Poyarkov, A. D., Rozhnov, V. V. (2019). POTENTIAL HABITAT OF SNOW LEOPARD (PANTHERA UNCIA, FELINAE) IN SOUTH SIBERIA AND ADJACENT TERRITORIES BASED ON THE MAXIMUM ENTROPY DISTRIBUTION MODEL.98(3), 332–342.
Abstract: The snow leopard is an endangered large felid inhabiting highlands of 12 Asian countries. It is distributed
across vast territories and adequate modern methods are required for mapping its potential habitats. The goal
of the present study is to create a model of snow leopard potential habitat within the northern part of its range
in Russia (and adjacent territories of Mongolia, China and Kazakhstan). More than 5 years of observations
(total number of presence points = 449), environmental variables and the maximum entropy distribution
method (Maxent) are used. The resulting map demonstrates that a suitable habitat (probability of the animal�s
presence between 0.5 and 1) of the northern population of snow leopard in Russia occupies 16500 km2
with a buffer of transient territories (probability between 0.25 and 0.49) covering 32800 km2. Most of a suitable
habitat within the study area is associated with the Altai Mountains, Western Sayan Mountains, Sangilen
Plateau, Tsagan-Shibetu and Shapshal. One third of the suitable habitat lies within areas of a varying protection
status. The results of modeling are of importance both for scientists and conservation managers, as they
allow for leopard occurrence to be predicted, supporting research on and the conservation of the species.
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Rana, B. S. (1997). Distinguishing kills of two large mammalian predators in Spiti Valley Himachal Pradesh. J.Bombay Nat.Hist.Soc, 94(3), 553.
Abstract: The author studied livestock killed by predators in the Spiti Valley, India, to determine what species had killed yaks, horses, donkeys, and other domestic animals. Eleven of the kills examined were made by snow leopards and six by the Tibetan wolf. Wolves were involved in surplus killings, while snow leopards kill as food is needed. lgh
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Christiansen, P. (2007). Canine morphology in the larger Felidae: implications for feeding ecology. Biological Journal of the Linnean Society, 91, 573–592.
Abstract: Canine morphology is analysed at seven intervals along the crown in both
anteroposterior and lateromedial perspective in seven species of large felids. The puma and the snow leopard have stout, rather conical canines, whereas those of lions, jaguars, and tigers bear substantial resemblance to each other, reflecting their phylogenetic relationships, and are less conical and large. The canines of the leopard are intermediate in morphology between those of the other species, probably reflecting its more generalized diet. The clouded leopard has very large and blade-like canines, which are different from the other analysed species. Canine bending strengths to estimated bite forces appear to differ less among the species than morphology,indicating that the evolution of canines has been constricted with respect to their strength in failure, probably owing to their being equally important for species fitness. However, the clouded leopard again stands out, having a high estimated bite force and rather weak canines in bending about the anteroposterior as well as lateromedial planes compared to the other species. Canine morphology to some extent reflects differences in killing mode, but also appears to be related to the phylogeny. The marked divergence of the clouded leopard is presently not understood.
Keywords: bite force, canine, clouded leopard, feeding behaviour, felid, Homotherium serum, leopard, Megantereoncultridens, morphology, Neofelis nebulosa, paleontology, Panthera pardus, Panthera tigris, puma, Puma concolor, Smilodon fatalis, Smilodon populator, snow leopard, Uncia uncia
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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.
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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.
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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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Oli, M. K., Taylor, I. R., & Rogers, M. E. (1994). Snow leopard Panthera unica predation of livestock: An assessment of local perceptions in the Annapurna Conservation Area, Nepal. Biological Conservation, 68(1), 63–68.
Abstract: Public attitudes towards snow leopard Panthera uncia predation of domestic livestock were investigated by a questionnaire survey of four villages in snow leopard habitat within the Annapurna Conservation Area, Nepal. Most local inhabitants were subsistence farmers, many dependent upon yaks, oxen, horses and goats, with an average livestock holding of 26.6 animals per household. Reported losses to snow leopards averaged 0.6 and 0.7 animals per household in two years of study, constituting 2.6% of total stockholding but representing in monetary terms almost a quarter of the average annual Nepali national per capita income. Local people held strongly negative attitudes towards snow leopards and most suggested that total extermination of leopards was the only acceptable solution to the predation problem. Snow leopards were reported to be killed by herdsmen in defence of their livestock. The long-term success of snow leopard conservation programmes may depend upon the satisfactory resolution of the predation conflict. Some possible ways of reducing predation losses are also discussed.
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