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Seidensticker, J., & Lumpkin, S. (1996). The adaptable leopard; unfortunately it's no match for modern man. Wildlife Conservation, 99(3), 52.
Abstract: Abstract: Leopards' adaptability has become the species' vulnerability. The animals do not hesitate to eat rotting flesh and will come back repeatedly to their meal, if disturbed. People have taken advantage of this by lacing carcasses with poison. Leopards are moderate in size compared to other cats, are stealthy and can live in areas as diverse as rain forests and deserts.
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Tursun, H., Wenhu, Y., & Meng, X. H. (2000). Great Exploitation of the West and the Basic Thoughts of the Great Development Strategy of Xinjiang. Arid Land Geography, 23(3), 193–198.
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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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Xu, F., Ming, M., Yin, S. -jing, & Munkhtsog, B. (2007). Investigation on Snow Leopard (Uncia uncia) and Its Prey in Baytag Mountain Region, Xinjiang (Vol. 21).
Abstract: The snow leopard and it s p rey were investigated in Beita Mountain Region , Xinjiang in Sep . 2004.
Both the field survey and questionnaire were involved in this project which was supported by the International
Snow Leopard Trust and Xinjiang Conservation Fund. The signs marked by the snow leopard were used
to reflect the living condition of snow leopard and they were collected by running transects. The prey investigation was conducted by positioned observation and route survey. Fifteen transects were done in the
project and 67 signs leaved by snow leopard were discovered in total. 58. 2 % of them were scrapes ,
35.8 % of t hem were feces , 4.5 % of them were claw rakes and 1. 5 % of them were scent
spray. As to the prey resources , 4 herds of 23 ibex and 24 herds of 418 chukars were found during the survey. Also 81 local people of 5 different nationalities were interviewed during the field work , 13.
58 % of them had seen the snow leopard , 20. 99 % of them had heard of snow leopard but not seen. Among t hem , 10 herdsmen had sufferred from the loss of livestock attacked by snow leopard.
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Yanfa, L. (1985). A preliminary investigation into the geographic distribution of the snow leopard Panthera uncia Schreber. Acta Theriologica Sinica, 5(3), 184–188.
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Anwar, M., Jackson, R., Nadeem, M., Janecka, J., Hussain, S., Beg, M., Muhammad, G., and Qayyum, M. (2011). Food habits of the snow leopard Panthera uncia (Schreber, 1775) in Baltistan, Northern Pakistan. European Journal of Wildlife Research, (3 March), 1–7.
Abstract: The snow leopard (Panthera uncia) inhabits the high, remote mountains of Pakistan from where very little information is available on prey use of this species. Our study describes the food habits of the snow leopard in the Himalayas and Karakoram mountain ranges in Baltistan, Pakistan. Ninety-five putrid snow leopard scats were collected from four sites in Baltistan. Of these, 49 scats were genetically confirmed to have originated from snow leopards. The consumed prey was identified on the basis of morphological characteristics of hairs recovered from the scats. It was found that most of the biomass consumed (70%) was due to domestic livestock viz. sheep (23%), goat (16%), cattle (10%), yak (7%), and cattle–yak hybrids (14%). Only 30% of the biomass was due to wild species, namely Siberian ibex (21%), markhor (7%), and birds (2%). Heavy predation on domestic livestock appeared to be the likely cause of conflict with the local inhabitants. Conservation initiatives should focus on mitigating this conflict by minimizing livestock losses.
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Watanabe, M., Sugano, S., Togashi, T., Imai, J., Uchida, K., Yamaguchi, R., et al. (2000). Molecular cloning and phylogenetic analysis of canine beta-casein. DNA Seq, 11(3-4), 295–300.
Abstract: A canine beta-casein cDNA was isolated from mammary tissue by polymerase chain reaction (PCR) using degenerate primers. It encodes 250 amino acids protein containing the conserved sequence motif of beta- casein. It showed the highest homology with snow-leopard (Uncia uncia (55-62% identity). It also showed 44-53% identity with human, 33-42%, identity with mouse, 29-37%, identity with rat, 43-53% identity with rabbit, 41-48% identity with pig, 44-51% identity with cattle and 44- 50% identity with sheep. A 1.2-kb mRNA was detected in mammary tissue by Northern blot analysis. Phylogenetic analysis revealed that canine beta-casein formed a branch with lesser panda and snow leopard, which were grouped into carnivore.
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Freeman, H., Braden, K. (1977). Zoo location as a factopr in the reproductive behavior of captive snow leopards, Uncia uncia. Zoological Garten J.F., 47(3/4), 280–288.
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Salles, L. O. (1992). Felid phylogenetics: Extant taxa and skull morphology (Felidae, Aeluroidae). American Museum Novitates, (3047), 1–67.
Abstract: relationships among extant felid taxa are controversial. A historical appraisal addresses component congruence among statements on felid phylogenetic relationships, and monophyly of generic ranks proposed for felids is discussed. Felid cranial morphology (especially the masticatory apparatus, basicranium, and rostral regions) is examined, and 44 characters are postulated for 39 taxa. Internal congruence for these characters is evaluated and 27 components are suggested. Parsimony analysis, using the successive weighting option of Hennig86, of the 44 cranial characters plus 13 other morphological features yields 29 components in a “modified Nelson” consensus cladogram. Two basal, well resolved clades are hypothesized in the total morphology analysis; under parenthetical notation the first is: (Hepailurus yagouaroundi (Puma concolor (Acinonyx jubatus (Uncia uncia (Neofelis nebulosa (Panthera tigris (P. onca, P. leo, and P. pardus)))))). The second clade is: Profelis temmincki (P. badia (Pardofelis marmorata ((Caracal caracal (Lynx rufus (L. lynx (L. pardina (L. canadensis)))) (Felis chaus (F. lybica (L. cafra (L. silvestris (F. bieti (F. nigripes (F. margarita (Octocolobus manul)))))))). Prionailurus planiceps and P. viverrina formed another group which is suggested as the basal branch of the felid phylogeny. The results in this study do not support monophyly of Leopardus Gray, 1841; Profelis Severtzon, 1858; and Prionailurus Severtzon, 1858. A better supported, more highly resolved, felid phylogenetic tree is needed.
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Koju, N. P., Gosai, K. R., Bashyal, B., Byanju, R., Shrestha, A., Buzzard, P., Beisch, W. B., Khanal, L. (2023). Seasonal Prey Abundance and Food Plasticity of the Vulnerable Snow Leopard (Panthera uncia) in the Lapchi Valley, Nepal Himalayas. Animals, 13(3182), 1–16.
Abstract: Conservation strategies for apex predators, like the snow leopard (Panthera uncia), depend on a robust understanding of their dietary preferences, prey abundance, and adaptability to changing ecological conditions. To address these critical conservation concerns, this study presents a comprehensive evidence on prey availability and preferences for snow leopards in the Lapchi Valley in the Nepal Himalayas from November 2021 to March 2023. Field data were collected through the installation of twenty-six camera traps at 16 strategically chosen locations, resulting in the recording of 1228 events of 19 mammalian species, including domesticated livestock. Simultaneously, the collection of twenty snow leopard scat samples over 3800 m above sea level allowed for a detailed dietary analysis. Photo capture rate index and biomass composition analysis were carried out and seasonal prey availability and consumption were statistically analyzed. A total of 16 potential prey species for the snow leopard were documented during the study period. Himalayan musk deer (Moschus leucogaster) was the most abundant prey species, but infrequent in the diet suggesting that are not the best bet prey for the snow leopards. Snow leopards were found to exhibit a diverse diet, consuming eleven prey species, with blue sheep (Pseudois nayaur) being their most consumed wild prey and horses as their preferred livestock. The Pianka’s index of dietary niche overlap between the summer and winter seasons were 0.576, suggesting a pronounced seasonal variation in food preference corroborating with the prey availability. The scarcity of larger preys in winter is compensated by small and meso-mammals in the diet, highlighting the snow leopard’s capacity for dietary plasticity in response to the variation in resource availability. This research suggests for the utilization of genetic tools to further explore snow leopard diet composition. Additionally, understanding transboundary movements and conducting population assessments will be imperative for the formulation of effective conservation strategies.
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