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.

Abstract: Excessive grazing by livestock is claimed to displace wild ungulates in the Trans-Himalaya. This study compares the seasonal diets and habitat use of sympatric wild naur Pseudois nayaur and domestic goat Capra hircus, sheep Ovis aries and free-ranging yak Bos grunniens in north Nepal and analyses their overlap both within and across seasons. Alpinemeadow and the legumes Oxytropis and Chesneya were critical resources for all animal groups. High overlap occurred cross-seasonally when smallstock (sheep and goats) in summer used the spring and autumn ranges of naur. Relatively high total ungulate biomass (3028 kg km-2) and low recruitment of naur (56 young per 100 adult females in autumn) suggested interspecific competition. The spatio-temporal heterogeneity in composition and phenology of food plants across the steep gradient of altitude, together with rotational grazing, appears to indirectly facilitate coexistence of naur and smallstock. However, owing to high crossseasonal (inter-seasonal) overlaps, competition is likely to occur between these two groups at high stocking densities. Within seasons, naur overlapped more with free-ranging yak than with smallstock. As their habitat use and diets were most similar in winter, when both fed extensively on the same species of shrubs, naur was most likely to compete with yak during that season.



Abstract: This study was undertaken in the Phu valley of Manang district in the Annapurna Conservation Area, Nepal,
Spring, 2004 and 2005. I used the Snow Leopard Management Information System (“second order” survey technique), to determine
the relative abundance of snow leopards in delineated areas in Phu valley. Transects routes were plotted by
randomly selected feasible landforms such as along ridgelines, cliff bases and river bluffs where snow
leopards sign is likely to be found. Altogether, 16 transects (total length of 7.912 km) were laid down (mean
transect length=0.495 km). They revealed, 54 sign sites (both relic and non-relic) and altogether 88 signs (72
scrapes, 11 feces, 3 scent mark, 2 pugmarks and 1 hair) were recorded (6.8 site/km and 11.1 signs/km). There
were 61.1% non-relic and 38.9% relic sites. The density of snow leopards in Phu Valley may be 4-5 snow
leopards/100 kmý.It was found that the Ghyo block had the highest sign density (13.6 mean sign item/km)
and Phu block (9.8 mean sign item/km) and the lowest in Ngoru block (3.9 mean sign item/km.). For blue sheep, direct count method was applied from different appropriate vantage points (fixed-point
count). I counted total individuals in each herd and classified all individuals whenever possible, using 8 X24
binocular and 15-60x spotting scope. A total 37 blue sheep herds and 1209 individuals were observed in
192.25 kmý of the study area (blue sheep density, 6.3 kmý). Average herd size was 32.68. Herd size varied
from 1 to 103 animals (the largest so far recorded). The average sex ratio male to female for the entire survey
area was 0.67. Recruitment rate was 47.13. The ratio of yearlings to adult female was 0.45. In Ghyo block
had total 168 blue sheep (area, 44.08 km2 or 3.8/ km2 i.e. 137.2 kg/ kmý). Blue sheep density in Ngoru block
showed 4.7/km2 (area, 65.47 km2). Highest density of blue sheep among three blocks was recorded in Phu
block, 8.9/km2 (or 320 kg/km2) in its 82.70 km2 area. A standard questionnaire was designed, and interviews conducted for relevant information was collected on
livestock depredation patterns (total household survey). Out of 33 households surveyed, 30 reported that they
had livestock depredation by the snow leopard in 2004. Altogether 58 animals were reportedly lost to snow
leopards (3.1% of the total mortality). Out of the estimated standing available biomass (1, 83,483kg) in the
Phu valley at least 2220 kg or 1.3% of the total livestock biomass was consumed by snow leopards in the
year of our study (2004). It was estimated that in the Phu valley annually 1.8 animals were lost per household
to snow leopards. This means approx. Rs.413560 (US$ 5,908) is lost annually in the valley (US$
179/household/annum). Ghyo block, had the highest animals loss (53.4%), followed by Phu block (36.2%)
and Ngoru block (10.3%) to snow leopards. There is positive correlation among the densities of blue sheep, relative abundance of the snow leopard and
livestock depredation. Blue sheep is the main prey species of the snow leopard in Phu valley and its
conservation therefore matters to reduce livestock depredation. A general patterns appears here that shows
that blue sheep (prey) abundance determine snow leopard (predator) abundance and that livestock
depredation by snow leopards may be minimal where there is good population of blue sheep, and vice versa.

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.

Abstract: In Nepal, naur are usually the staple wild prey for the snow leopard, a solitary stalker hunter, and in some cases, for the wolf who hunts in a pack. We assumed that naur would adapt their anti-predatory responses to the presence of chasing and ambushing predators in the Manang Valley, where there are snow leopards and wolves, and in the Nar Phu valley, an area where there is only the snow leopard.
Aims. The aim of this study was to determine if there were differences in anti-predator strategies (vigilance, habitat selection and escape terrain) of naur in two valleys over two seasons, spring and autumn.
Methods. In spring 2019, we conducted a reconnaissance survey on the status of the naur and its habitat in the Manang and Nar Phu valleys of the Annapurna Conservation Area, Nepal. In spring and autumn 2020 and 2021, we observed 360 focal naur individuals (180 individuals in each valley), using the vigilance behaviour methodology to examine the behaviour of the naur.
Key results. There was little difference in the size of the naur groups between the Manang and Nar Phu valleys. The naur were twice as vigilant in Manang (15%), where there are snow leopards and wolves, as they were in Nar Phu (9%), with only snow leopards. The distance from the naur to escape cover was significantly shorter in Manang than in Nar Phu valley. Naur used significantly more rolling terrain in Nar Phu than in Manang. Conclusions. The return of wolves to the Manang valley may have resulted in an increase in the level of naur vigilance. Most likely, the wolves in Manang have already had an effect on the female-to-young-ratio, and this effect will possibly have important consequences for the naur population, as well as at the ecosystem level in the future. Other key determining factors, such as the climate crisis and changes in local resources, could have a significant impact on the naur population, indicating the need for more research. Implications. The findings of this study would provide valuable baseline information for the design of a science-based conservation strategy for conservation managers and scientists on naur, snow leopards and wolves.