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Sangay, T., & Vernes, K. (2008). Human-wildlife conflict in the Kingdom of Bhutan: Patterns of livestock predation by large mammalian carnivores (Vol. 141).
Abstract: We examined predation activity throughout Bhutan by tiger (Panthera tigris), common leopard (Panthera pardus), snow leopard (Uncia uncia) and Himalayan black bear (Ursus thibetanus) on a variety of livestock types using data gathered over the first two years (2003-2005) of a compensation scheme for livestock losses. One thousand three hundred and seventy five kills were documented, with leopards killing significantly more livestock (70% of all kills),
than tigers (19%), bears (8%) and snow leopards (2%). About 50% of livestock killing were of cattle, and about 33% were of horses, with tigers, leopards and snow leopards killing a significantly greater proportion of horses than predicted from availability. Examination of cattle kills showed that leopards killed a significantly greater proportion of smaller prey (e.g., calves), whereas tigers killed a significantly greater proportion of larger prey (e.g., bulls). Overall, livestock predation was greatest in summer and autumn which corresponded with a peak in cropping agriculture; livestock are turned out to pasture and forest during the cropping season, and subsequently, are less well guarded than at other times. Across Bhutan, high horse density and low cattle and yak density were associated with high rates of livestock attack, but no relationship was found with forest cover or human population density. Several northern districts were identified as 'predation hotspots', where proportions of livestock lost to predation were considerable, and the ratio of reported kills to relative abundance of livestock was high. Implications of our findings for mitigating livestock losses and for conserving large carnivores in Bhutan are discussed.
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Schaller, G. B. (1977). Mountain Monarchs: Wild Sheep and Goats of the Himalaya (Wildlife Behavior & Ecology). Chicago: University of Chicago Press.
Abstract: Describes snow leopard status and field observations from studies in Pakistan and Nepal. Review provides some data on snow leopard marking behavior, social relations, food habits and predator behavior.
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Schaller, G. B. (1980). Stones of Silence: Journeys in the Himalaya. New York: Viking Press.
Abstract: Anecdotal description of wildlife field studies in the Himalaya, including information on snow leopard natural history and an encounter with snow leopards in Pakistan.
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Sharma, R. K., Bhatnagar, Y. V., Mishra, C. (201). Does livestock benefit or harm snow leopards? Biological Conservatio, (190), 8–13.
Abstract: Large carnivores commonly prey on livestock when their ranges overlap. Pastoralism is the dominant land use type across the distributional range of the endangered snow leopard Panthera uncia. Snow leop- ards are often killed in retaliation against livestock depredation. Whether livestock, by forming an alter- native prey, could potentially benefit snow leopards, or, whether livestock use of an area is detrimental to snow leopards is poorly understood. We examined snow leopard habitat use in a multiple use landscape that was comprised of sites varying in livestock abundance, wild prey abundance and human population size. We photographically sampled ten sites (average size 70 sq. km) using ten camera traps in each site, deployed for a period of 60 days. Snow leopard habitat use was computed as a Relative Use Index based on the total independent photographic captures and the number of snow leopard individuals captured at each site. We quantified livestock abundance, wild prey abundance, human population size and terrain ruggedness in each of the sites. Key variables influencing snow leopard habitat use were identified using Information Theory based model selection approach. Snow leopard habitat use was best explained by wild prey density, and showed a positive linear relationship with the abundance of wild ungulates. We found a hump-shaped relationship between snow leopard habitat use and livestock stocking density, with an initial increase in habitat use followed by a decline beyond a threshold of livestock density. Our results suggest that in the absence of direct persecution of snow leopards, livestock grazing and snow leopard habitat use are potentially compatible up to a certain threshold of livestock density, beyond which habitat use declines, presumably due to depressed wild ungulate abundance and associated anthropogenic disturbance.
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Sharma, S., Thapa, K., Chalise, M., Dutta, T., Bhatnagar, Y.V., McCarthy, T. (2006). The snow leopard in Himalaya: A step towards their conservation by studying their distribution, marking habitat selection, coexistence with other predators, and wild prey-livestock-predator interaction. Conservation Biology in Asia, , 184–196.
Abstract: Snow leopard (Uncia uncial) is a flagship species of the Himalaya. Very few studies have been done on the ecology of this species in the Himalaya. This paper presents an overview of four studies conducted on snow leopards in Nepal and India, dealing with various aspects of snow leopard ecology including their status assessment, making behaviour, habitat selection, food habits, and impact on livestock. The information generated by these studies is useful in planning effective conservation and management strategies for this endangered top predator of high mountains.
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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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Shrestha, R., & Wegge, P. (2006). Determining the composition of herbivore diets in the Trans-Himalayan rangelands: A comparison of field methods. Journal of Rangeland Ecology and Management, 59(5), 512–518.
Abstract: In late summer, in a semi-arid mountain range in Nepal, we compared 3 field methods for determining the botanical composition of herbivore diets. Data were collected from the same animals belonging to 1 herd of domestic yak (Bos grunniens) and 2 herds of mixed smallstock, consisting of domestic goats (Capra hircus) and sheep (Ovis aries). Bite count, feeding site examination, and microhistological analysis of feces gave different estimates of forage categories and plant species in both animal groups. Because yaks grazed in other vegetation communities when not observed for bite-counts and feeding signs, the results from the latter methods could not be compared directly with that from fecal analysis. In smallstock, feeding site examination gave higher estimates of graminoids and lower estimates of shrubs than the other 2 methods, probably because all feeding signs on shrubs were not detected. Bite-counts and fecal analysis gave comparable results, except that forbs were underestimated by fecal analysis, presumably due to their more complete digestion. Owing to the difficulty in collecting samples that are representative of the entire grazing period and the problem of recording feeding signs correctly, both feeding site examination and bite-counts are unsuitable methods for studying the food habits of free ranging domestic and wild herbivores. Microhistological analysis of feces appears to be the most appropriate method, but correction factors are needed to adjust for differential digestion. The systematic use of photomicrographs improves the speed and accuracy of the fecal analysis.
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Shrestha, R., & Wegge, P. (2008). Habitat relationships between wild and domestic herbivores in Nepalese trans – Himalaya. Journal of Arid Environments, 72, 914–925.
Abstract: In the semi-arid ecosystems of Asia, where pastoralism is a main subsistence occupation, grazing competition from domestic stock is believed to displace the wild ungulates. We studied the habitat relationships among sympatric naur and domestic yak and smallstock in Phu valley in upper Manang district, Nepal, on the basis of their distribution on vegetation types, elevation and slope. To control for the disturbance effect by humans, we collected the data on naur from those ranges where domestic stock were not being attended by herders. We applied correspondence analysis to explore habitat associations among animal groups (n ¬ 1415) within and across-seasons. Within each association, interspecific habitat overlaps and species habitat preferences were calculated. Naur was strongly associated with free-ranging yak as they used similar altitudinal ranges in all seasons, except in spring. Their distributions on vegetation types and slopes were also quite similar, except for a stronger preference for alpine meadows by naur during summer and winter. Naur and smallstock did not form temporal associations as the latter consistently used lower elevations. In autumn and spring, however, naur spatially overlapped with the summer range of smallstock, and both preferred the alpine meadow habitat during these periods. Alpine meadow was the least abundant vegetation type but was consistently and preferentially used by all animal groups across seasons. At high stocking densities, all three animals groups are therefore likely to compete for this vegetation type. The role of spatio-temporal heterogeneity for interpreting the interspecific relationships among ungulates in the semi-arid rangelands of the trans-Himalaya is discussed.
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Singh, S. K., De, R., Sharma, R., Maheshwari, A., Joshi, B. D., Sharma, D., Sathyakumar, S., Habib, B., Goyal, S. P. (2022). Conservation importance of the strategic, centrally located snow leopard population in the western Himalayas, India: a genetic perspective. Mammalian Biology, , 13.
Abstract: The snow leopard population in Union Territory of Ladakh (UTL), India is at the centre of five out of eight mountain ranges within the species' habitat in the high-mountain Asia. Its strategic location is of immense conservation significance to maintain genetic connectivity and metapopulation dynamics of snow leopards (Panthera uncia). Therefore, we provide the first estimates of the snow leopard's individual-based spatial genetic characteristics from UTL. Multi-locus genotyping (n = 14 loci) of individuals (n = 19) revealed moderate genetic diversity in the population (mean number of alleles = 5.86 ± 0.55, observed heterozygosity = 0.48 ± 0.05, expected heterozygosity = 0.65 ± 0.03, allelic richness = 2.65 ± 0.15). We did not observe any evidence of population structuring (using STRUCTURE and Factorial Correspondence Analysis) or isolation by distance. However, the clustering approach based on genetic distance (Nei's standard distance and Cavalli-Sforza and Edwards distance) and subsequent discriminant analysis of principal components (DAPC) revealed three sub-clusters of related individuals within the study population without any spatial correlates. We observed 1.2% first-order relatives, suggesting sufficient dispersal and panmixia in the UTL population. We observed high fixation index (FIS = 0.26 ± 0.05; 0.17 ± 0.03 upon removing loci with null alleles) and presence of individuals from genetically divergent populations in UTL. Hence, the high positive FIS value could be attributed to both Wahlund effect and inbreeding. Prioritization and effective conservation planning of the UTL population as a source would benefit the global snow leopard population by (i) maintaining connectivity between the Himalayas and the central Asian mountain ranges, and (ii) providing refuge during future climate change-related range contraction.
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Stockley, G. (1936). Stalking in the Himalayas and Northern India. London: Herbert Jenkins.
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