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Ahlborn, G., & Jackson, R. M. (1988). Marking in Free-Ranging Snow Leopards in West Nepal: A preliminary assesment. In H.Freeman (Ed.), (pp. 25–49). India: Snow Leopard Trust and the Wildlife Institute of India.
Abstract: Describes and Quantifies snow leopard marking behaviour, based primarily on sign, gatherd during a four year study in Nepal. Emphasis is on scrapes and spray markings, detailing their frequency of occurence realtive to habitat characteristics and season. Both sexes mark intensively, sign abundance is associated with intensity of use, and sign is concentrated along breaks in terrain.
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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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Aryal, A. (2009). Final Report On Demography and Causes of Mortality of Blue Sheep (Pseudois nayaur) in Dhorpatan Hunting Reserve in Nepal.
Abstract: A total of 206 individual Blue sheep Pseudois nayaur were estimated in Barse and Phagune blocks of Dhorpatan Hunting Reserve (DHR) and population density was 1.8 Blue sheep/sq.km. There was not significant change in population density from last 4 decades. An average 7 animals/herd (SD-5.5) were classified from twenty nine herds, sheep per herds varying from 1 to 37. Blue sheep has classified into sex ratio on an average 75 male/100females was recorded in study area. The sex ratio was slightly lower but not significantly different from the previous study. Population of Blue sheep was seen stable or not decrease even there was high poaching pressure, the reason may be reducing the number of predators by poison and poaching which has
supported to increase blue sheep population. Because of reducing the predators Wolf Canis lupus, Wild boar population was increasing drastically in high rate and we can observed wild boar above the tree line of DHR. The frequency of occurrence of different prey species in scats of different predators shows that, excluding zero values, the frequencies of different prey species were no significantly different (ö2= 10.3, df = 49, p > 0.05). Most of the scats samples (74%) of Snow leopard, Wolf, Common Leopard, Red fox's cover one prey species while two and three species were present in 18% and 8%, respectively. Barking deer Muntiacus muntjak was the most frequent (18%) of total diet composition of common leopards. Pika Ochotona roylei was the most frequent (28%), and Blue sheep was in second position for diet of snow leopards which cover 21% of total diet composition. 13% of diet covered non-food item such as soil, stones, and vegetable. Pika was most frequent on Wolf and Red fox diet which covered 32% and 30% respectively. There was good positive relationship between the scat density and Blue sheep consumption rate, increasing the scat density, increasing the Blue sheep consumption rate. Blue sheep preference by different predators such as Snow leopard, Common leopard, Wolf and Red fox were 20%, 6%, 13% and 2% of total prey species respectively.
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Chundawat, R. S. (1993). Studies on Snow Leopard and Prey Species in Hemis National Park (Vol. xi). Seattle: Islt.
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Chundawat, R. S., & Rawat G.S. (1990). Food Habits of Snow Leopard in Ladakh, India.
Abstract: The snow leopard has remained little studied in the past, and most of the information available is either in the form of natural history or anecdotal notes. The inaccessibility of the terrain and its secretive habits make this one of the more difficult animals to study in the wild. In the past decade, several ecological surveys were conducted in India, Nepal, China and Mongolia, which gave us information on the status and distribution of snow leopard (Jackson, Mallon, Fox, Schaller, Chundawat) A detailed study in Nepal through light on its secretive habits ( Jackson and Ahlborn, 1989). Even then little is known about its feeding habits. The present paper discusses this aspect from a study which was part of a detailed study conducted on the ecology of snow leopard in India from October 1987 to Feburary 1990.
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Henschel, P., & Ray, J. (2003). Leopards in African Rainforests: Survey and Monitoring Techniques (Wildlife Conservation Society, Ed.).
Abstract: Monitoring Techniques Forest leopards have never been systematically surveyed in African forests, in spite of their potentially vital ecological role as the sole large mammalian predators in these systems. Because leopards are rarely seen in this habitat, and are difficult to survey using the most common techniques for assessing relative abundances of forest mammals, baseline knowledge of leopard ecology and responses to human disturbance in African forests remain largely unknown. This technical handbook sums up the experience gained during a two-year study of leopards by Philipp Henschel in the Lop‚ Reserve in Gabon, Central Africa, in 2001/2002, supplemented by additional experience from carnivore studies conducted by Justina Ray in southwestern Central African Republic and eastern Congo (Zaire) . The main focus of this effort has been to develop a protocol that can be used by fieldworkers across west and central Africa to estimate leopard densities in various forest types. In developing this manual, Henschel tested several indirect methods to assess leopard numbers in both logged and unlogged forests, with the main effort devoted to testing remote photography survey methods developed for tigers by Karanth (e.g., Karanth 1995, Karanth & Nichols 1998; 2000; 2002), and modifying them for the specific conditions characterizing African forest environments. This handbook summarizes the results of the field testing, and provides recommendations for techniques to assess leopard presence/absence, relative abundance, and densities in African forest sites. We briefly review the suitability of various methods for different study objectives and go into particular detail on remote photography survey methodology, adapting previously developed methods and sampling considerations specifically to the African forest environment. Finally, we briefly discuss how camera trapping may be used as a tool to survey other forest mammals. Developing a survey protocol for African leopards is a necessary first step towards a regional assessment and priority setting exercise targeted at forest leopards, similar to those carried out on large carnivores in Asian and South American forests.
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Hol, E. H., & Marden, T. (1994). Methods for Sampling and Analysis to establish potential exposure of wildlife to persistent contaminants in remote areas. In J.L.Fox, & D.Jizeng (Eds.), (pp. 279–287). Usa: Islt.
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Hung, L., Talipu, Hua, L., Mingjiang, Q., & Schaller, G. B. (1985). A Snow Leopard Survey in the Taxkorgan Region, XInjiang, China.
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Jackson, R. (1992). SSC Plan for Snow Leopard.
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Jackson, R., Zongyi, W., Xuedong, L., & Yun, C. (1994). Snow Leopards in the Qomolangma Nature Preserve of Tibet Autonomous Region. In J.L.Fox, & D.Jizeng (Eds.), (pp. 85–95). Usa: Islt.
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Janecka, J.E., Jackson, R., Yuquang, Z., Diqiang, L., Munkhtsog, B., et al. (2008). Population monitoring of snow leopards using noninvasive collection of scat samples: a pilot study (Vol. 11).
Abstract: The endangered snow leopard Panthera uncia occurs in rugged, high-altitude regions of Central Asia. However, information on the status of this felid is limited in many areas. We conducted a pilot study to optimize molecular markers for the analysis of snow leopard scat samples and to examine the feasibility of using noninvasive genetic methods for monitoring this felid. We designed snow leopard-specific primers for seven microsatellite loci that amplified shorter segments and avoided flanking sequences shared with repetitive elements. By redesigning primers we maximized genotyping success and minimized genotyping errors. In addition, we tested a Y chromosome-marker for sex identification and designed a panel of mitochondrial DNA primers for examining genetic diversity of snow leopards using scat samples. We collected scats believed to be from snow leopards in three separate geographic regions including north-western India, central China and southern Mongolia. We observed snow leopard scats in all three sites despite only brief 2-day surveys in each area. There was a high rate of species misidentification in the field with up to 54% of snow leopard scats misidentified as red fox. The high rate of field misidentification suggests sign surveys incorporating scat likely overestimate snow leopard abundance. The highest ratio of snow leopard scats was observed in Ladakh (India) and South Gobi (Mongolia), where four and five snow leopards were detected, respectively. Our findings describe a species-specific molecular panel for analysis of snow leopard scats, and highlight the efficacy of noninvasive genetic surveys for monitoring snow leopards. These methods enable large-scale noninvasive studies that will provide information critical for conservation of snow leopards.
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Jumabay, K., Wegge, P., Mishra, C., Sharma, K. (2013). Large carnivores and low diversity of optimal prey: a comparison of the diets of snow leopards Panthera uncia and wolves Canis lupus in Sarychat-Ertash Reserve in Kyrgyzstan. Oryx, , 1–7.
Abstract: In the cold and arid mountains of Central Asia, where the diversity and abundance of wild ungulates
are generally low, resource partitioning among coexisting carnivores is probably less distinct than in prey-rich areas. Thus, similar-sized carnivores are likely to compete for food. We compared the summer diets of snow leopards Panthera uncia and wolves Canis lupus in Sarychat-Ertash Reserve in the Tien-Shan mountains of Kyrgyzstan, based on analysis of genetically confirmed scats. Abundances of
the principal prey species, argali Ovis ammon and Siberian ibex Capra sibirica, were estimated from field surveys. The diets consisted of few species, with high interspecific overlap (Pianka’s index50.91). Argali was the predominant prey, with .50% frequency of occurrence in both snow leopard and wolf scats. This was followed by Siberian ibex and marmots Marmota baibacina. Being largely unavailable, remains of livestock were not detected in any of the scats. In the snow leopard diet, proportions of argali and ibex were in
line with the relative availabilities of these animals in the Reserve. This was in contrast to the diet of wolf, where argali occurred according to availability and ibex was significantly underrepresented. The high diet overlap indicates that the two predators might compete for food when the diversity of profitable, large prey is low. Competition may be more intense in winter, when marmots are not available. Hunting of argali and ibex outside the Reserve may be unsustainable and therefore reduce their abundances over time. This will
affect both predators negatively and intensify competition for food. Reduction in ibex populations will directly affect the snow leopard, and the wolf is likely to be indirectly affected as a result of increased snow leopard predation of argali.
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Karmacharya, D. (2011). Field Protocol – Scat Collection for Genetic Analysis.
Abstract: Project funded by Snow Leopard Conservation Grant Program. Center for Molecular Genetics, Nepal.
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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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Koshkarev, E. (1997). Has the Snow Leopard Disappeared from Eastern Sayan and Western Hovsogol? In R.Jackson, & A.Ahmad (Eds.), (pp. 96–107). Lahore, Pakistan: Islt.
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Koshkarev, E. (1998). Snow leopard along the border of Russia and Mongolia. Cat News, 28, 12–14.
Abstract: The author discusses the distribution of snow leopards along the border of Russia and Mongolia. The range extension of the leopard indicates their ability to cross desert areas that separate mountain habitats.habitat; range extension; scat analysis; techniques; tracks/tracking | snow leopard
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Kyes, R., & Chalise, M. K. (2005). Assessing the Status of the Snow Leopard Population in Langtang National Park, Nepal.
Abstract: This project is part of an ongoing snow leopard study established in 2003 with support from the ISLT. The study involves a multifaceted approach designed to provide important baseline data on the status of the snow leopard population in Langtang National Park (LNP), Nepal and to generate long-term support and commitment to the conservation of snow leopards in the park. The specific aims include: 1) conducting a population survey of the snow leopards in LNP, focusing on distribution and abundance; 2) assessing the status of prey species populations in the park; and 3) providing educational outreach programs on snow leopard conservation for local school children (K-8) living in the park. During the 2004 study period, snow leopard signs were observed (including pugmarks and scats) although somewhat fewer than in 2003. Similarly, the average herd size of the snow leopards' primary prey species in LNP (the Himalayan thar) was a bit lower than in 2003. There is speculation that the thar populations and the snow leopards may be moving to more remotes areas of the park perhaps in response to increasing pressure from domestic livestock grazing. This possibility is being addressed during the 2005 study period.
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Lovari, S., Boesi, R., Minder, I., Mucci, N., Randi, E., Dematteis, A., and Ale, S. B. (2009). Restoring a keystone predator may endanger a prey species in a human-altered ecosystem: the return of the snow leopard to Sagarmatha National Park. Animal Conservation, 12, 559–570.
Abstract: Twenty-five years ago, the snow leopard Uncia uncia, an endangered large cat, was eliminated from what is now Sagarmatha National Park (SNP). Heavy hunting pressure depleted that area of most medium-large mammals, before it became a park. After three decades of protection, the cessation of hunting and the recovery of wild ungulate populations, snow leopards have recently returned (four individuals). We have documented the effects of the return of the snow leopard on the population of its main wild prey, the Himalayan tahr Hemitragus jemlahicus, a 'near-threatened' caprin. Signs of snow leopard presence were recorded and scats were collected along a fixed trail (130 km) to assess the presence and food habits of the snow leopard in the Park, from 2004 to 2006. Himalayan tahr, the staple of the diet, had a relative occurrence of 48% in summer and 37% in autumn, compared with the next most frequent prey, musk deer Moschus chrysogaster (summer: 20%; autumn: 15%) and cattle (summer: 15%; autumn: 27%). In early summer, the birth rate of tahr (young-to-female ratio: 0.8-0.9) was high. The decrease of this ratio to 0.1-0.2 in autumn implied that summer predation concentrated on young tahr, eventually altering the population by removing the kid cohort. Small populations of wild Caprinae, for example the Himalayan tahr population in SNP, are sensitive to stochastic predation events and may be led to almost local extinction. If predation on livestock keeps growing, together with the decrease of Himalayan tahr, retaliatory killing of snow leopards by local people may be expected, and the snow leopard could again be at risk of local extinction. Restoration of biodiversity through the return of a large predator has to be monitored carefully, especially in areas affected by humans, where the lack of important environmental components, for example key prey species, may make the return of a predator a challenging event.
Keywords: conservation, food habits, genetics, Hemitragus jemlahicus, Himalayan tahr, management, microsatellite, predation, presence, scat, scat analysis, snow leopard, Uncia uncia
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Oli, M. K. (1993). A key for the identification of the hair of mammals of a snow leopard (Panthera uncia) habitat in Nepal. Journal of Zoology London, 231(1), 71–93.
Abstract: Analysis of prey remains in scats, particularly hairs, in widely used to study diet of mammalian predators, but identification of hair is often difficult because hair structures vary considerably both within and between species. Use of photographic reference of diagnostically important hair structures from mammals occurring in a predator's habitat has been found to be convenient for routine identification. A photographic reference key was developed for the identification of hairs of the mammals known to occur in a snow leopard (Panthera uncia) habitat in the Annapurna Conservation Area, Nepal. The key included a photographic reference of the diagnostic hair structures of nine species of wild and five species of domestic mammals. The cross-sectional appearance, shape and arrangement of medulla, the ratio of cortex to medulla, and the form and distribution of pigment in medulla and cortex were important diagnostic aids in the identification of hairs.
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Oli, M. K. (1994). Snow leopards and local human population in a protected area: a case study from the Nepalese Himalaya. In J.L.Fox, & D.Jizeng (Eds.), (pp. 51–64). Usa: International Snow Leopard Trust, Seattle, Washington.
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Oli, M. K., Taylor, I. R., & Rogers, M. K. (1993). Diet of the snow leopard (Panthera uncia) in the Annapurna Conservation Area, Nepal. Journal of Zoology London, 231(3), 365–370.
Abstract: The diet of the snow leopard (Panthera uncia) was studied from 213 scats collected between April 1990 and February 1991 in the Annapurna Conservation Area, Nepal. Seven species of wild and five species of domestic mammals were taken, as well as an unidentified mammal and birds. Blue sheep (Pseudois nayaur) were the most frequently eaten prey. Himalayan marmots (Marmota himalayana) were also important, except in winter when they were hibernating. During winter, snow leopards ate more Royle's pika (Ochotona roylei) and domestic livestock. Yaks were eaten more frequently than other livestock types.
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Pal, R., Panwar, A., Goyal, S. P., Sathyakumar, S. (2022). Changes in ecological conditions may influence intraguild competition: inferring interaction patterns of snow leopard with co-predators. PeerJ, 10(e14277), 1–26.
Abstract: Background: Large-scale changes in habitat conditions due to human modifications and climate change require management practices to consider how species communities can alter amidst these changes. Understanding species interactions across the gradient of space, anthropogenic pressure, and season provide the opportunity to anticipate possible dynamics in the changing scenarios. We studied the interspecific interactions of carnivore species in a high-altitude ecosystem over seasonal (summer and winter) and resource gradients (livestock grazing) to assess the impact of changing abiotic and biotic settings on coexistence.
Methods: The study was conducted in the Upper Bhagirathi basin, Western Himalaya, India. We analyzed around 4 years of camera trap monitoring data to understand seasonal spatial and temporal interactions of the snow leopard with common leopard and woolly wolf were assessed in the greater and trans-Himalayan habitats, respectively. We used two species occupancy models to assess spatial interactions, and circadian activity patterns were used to assess seasonal temporal overlap amongst carnivores. In addition, we examined scats to understand the commonalities in prey selection.
Results: The result showed that although snow leopard and wolves depend on the same limited prey species and show high temporal overlap, habitat heterogeneity and differential habitat use facilitate co-occurrence between these two predators. Snow leopard and common leopard were spatially independent in the summer. Conversely, the common leopard negatively influences the space use of snow leopard in the winter. Limited prey resources (lack of livestock), restricted space (due to snow cover), and similar activity patterns in winter might result in strong competition, causing these species to avoid each other on a spatial scale. The study showed that in addition to species traits and size, ecological settings also play a significant role in deciding the intensity of competition between large carnivores. Climate change and habitat shifts are predicted to increase the spatial overlap between snow leopard and co-predators in the future. In such scenarios, wolves and snow leopards may coexist in a topographically diverse environment, provided sufficient prey are available. However, shifts in tree line might lead to severe competition between common leopards and snow leopards, which could be detrimental to the latter. Further monitoring of resource use across abiotic and biotic environments may improve our understanding of how changing ecological conditions can affect resource partitioning between snow leopards and predators.
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Schaller, G. B. (1972). On the behaviour of Blue Sheep (Pseudois nayaur). Journal of Bombay Natural Historical Society, 69, 523–537.
Abstract: Two or three snow leopards hunted in the study area in eastern Nepal. Describes content of some snow leopard scat
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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.
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Shrestha, B. (2008). Prey Abundance and Prey Selection by Snow Leopard (uncia uncia) in the Sagarmatha (Mt. Everest) National Park, Nepal.
Abstract: Predators have significant ecological impacts on the region's prey-predator dynamic and community structure through their numbers and prey selection. During April-December 2007, I conducted a research in Sagarmatha (Mt. Everest) National Park (SNP) to: i) explore population status and density of wild prey species; Himalayan tahr, musk deer and game birds, ii) investigate diet of the snow leopard and to estimate prey selection by snow leopard, iii) identify the pattern of livestock depredation by snow leopard, its mitigation, and raise awareness through outreach program, and identify the challenge and opportunities on conservation snow leopard and its co-existence with wild ungulates and the human using the areas of the SNP. Methodology of my research included vantage points and regular monitoring from trails for Himalayan tahr, fixed line transect with belt drive method for musk deer and game birds, and microscopic hair identification in snow leopard's scat to investigate diet of snow leopard and to estimate prey selection. Based on available evidence and witness accounts of snow leopard attack on livestock, the patterns of livestock depredation were assessed. I obtained 201 sighting of Himalayan tahr (1760 individuals) and estimated 293 populations in post-parturient period (April-June), 394 in birth period (July -October) and 195 November- December) in rutting period. In average, ratio of male to females was ranged from 0.34 to 0.79 and ratio of kid to female was 0.21-0.35, and yearling to kid was 0.21- 0.47. The encounter rate for musk deer was 1.06 and density was 17.28/km2. For Himalayan monal, the encounter rate was 2.14 and density was 35.66/km2. I obtained 12 sighting of snow cock comprising 69 individual in Gokyo. The ratio of male to female was 1.18 and young to female was 2.18. Twelve species (8 species of wild and 4 species of domestic livestock) were identified in the 120 snow leopard scats examined. In average, snow leopard predated most frequently on Himalayan tahr and it was detected in 26.5% relative frequency of occurrence while occurred in 36.66% of all scats, then it was followed by musk deer (19.87%), yak (12.65%), cow (12.04%), dog (10.24%), unidentified mammal (3.61%), woolly hare (3.01%), rat sp. (2.4%), unidentified bird sp. (1.8%), pika (1.2%), and shrew (0.6%) (Table 5.8 ). Wild species were present in 58.99% of scats whereas domestic livestock with dog were present in 40.95% of scats. Snow leopard predated most frequently on wildlife species in three seasons; spring (61.62%), autumn (61.11%) and winter (65.51%), and most frequently on domestic species including dog in summer season (54.54%). In term of relative biomass consumed, in average, Himalayan tahr was the most important prey species contributed 26.27% of the biomass consumed. This was followed by yak (22.13%), cow (21.06%), musk deer (11.32%), horse (10.53%), wooly hare (1.09%), rat (0.29%), pika (0.14%) and shrew (0.07%). In average, domestic livestock including dog were contributed more biomass in the diet of snow leopard comprising 60.8% of the biomass consumed whilst the wild life species comprising 39.19%. The annual prey consumption by a snow leopard (based on 2 kg/day) was estimated to be three Himalayan tahr, seven musk deer, five wooly hare, four rat sp., two pika, one shrew and four livestock. In the present study, the highest frequency of attack was found during April to June and lowest to July to November. The day of rainy and cloudy was the more vulnerable to livestock depredation. Snow leopard attacks occurred were the highest at near escape cover such as shrub land and cliff. Both predation pressure on tahr and that on livestock suggest that the development of effective conservation strategies for two threatened species (predator and prey) depends on resolving conflicts between people and predators. Recently, direct control of free – ranging livestock, good husbandry and compensation to shepherds may reduce snow leopard – human conflict. In long term solution, the reintroduction of blue sheep at the higher altitudes could also “buffer” predation on livestock.
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