Abstract: Snow leopard survey was conducted in Oct-Nov 2004 at Tumor National Natural Reserve, Xinjiang, China. Because of its special living style, the snow leopard is difficult to observe by sight. Signs left by snow leopard become a good index to prove the existance of the big cat. There are mainly five kinds of signs, footprints, fectes, claw rakes and urine spray. From them we can know the distribution, probably population and habitat selection of snow leopard. This time in Tumor we investigated 5 difference places: Pochenzi in Mozat River area, Boxidun in Little Kuzbay River area, Yinyer in Tomur River area, Kurgan and Taglak in Quiong Tailan River area. 42 transects were run in this trip and a total of 57 signs found. Among them, footprints amounted to 71.9%, scrapes 21.1%, and feces 7.0%. The results showed that the big cat existed in Yinyer, Kurgan and Taglak areas and liked to select their habitat in the valley and didn't like to live in barren areas.

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.

Abstract: Many mammalian herbivores show a temporal diet variation between graminoid-dominated and browse dominated diets. We determined the causes of such a diet shift and its implications for conservation of a medium sized ungulate-the bharal Pseudois nayaur. Past studies show that the bharal diet is dominated by graminoids (>80%) during summer, but the contribution of graminoids declines to about 50% in winter. We tested the predictions generated by two alternative hypotheses explaining the decline: low graminoid availability during winter causes bharal to include browse in their diet; bharal include browse, with relatively higher nutritional quality, in their diet to compensate for the poor quality of graminoids during winter. We measured winter graminoid availability in areas with no livestock grazing, areas with relatively moderate livestock grazing, and those with intense livestock grazing pressures. The chemical composition of plants contributing to the bharal diet was analysed. The bharal diet was quantiWed through signs of feeding on vegetation at feeding locations. Population structures of bharal populations were recorded using a total count method. Graminoid availability was highest in areas without livestock grazing, followed by areas with moderate and intense livestock grazing. The bharal diet was dominated by graminoids (73%) in areas with highest graminoid availability. Graminoid contribution to the bharal diet declined monotonically (50, 36%) with a decline in graminoid availability. Bharal young to female ratio was 3 times higher in areas with high graminoid availability than areas with low graminoid availability. The composition of the bharal winter diet was governed predominantly by the availability of graminoids in the rangelands. Our results suggest that bharal include more browse in their diet during winter due to competition from livestock for graminoids. Since livestock grazing reduces graminoid availability, creation of livestock-free areas is necessary for the conservation of grazing species such as the bharal and its predators including the endangered snow leopard in the Trans-Himalaya.

Abstract: The main purpose of this work was to study the use of infrared trapping cameras to estimate snow leopard Uncia uncia population size in a specific study area. This is the first time a study of this nature has taken place in China. During 71 days of field work, a total of 36 cameras were set up in five different small vales of the Muzat Valley adjacent to the Tomur Nature Reserve in Xinjiang Province, E80ø35' – 81ø00' and N42ø00' – 42ø10', elevation 2'300 – 3'000 m, from 18th October to 27th December 2005. We expended approximately 2094 trap days and nights total (c. 50'256 hours). At least 32 pictures of snow leopards, 22 pictures of other wild species (e.g. chukor, wild pig, ibex, red fox, cape hare) and 72 pictures of livestock were taken by the passive Cam Trakker (CT) train monitor in about 16 points of the Muzat Valley. The movement distance of snow leopard was 3-10 km/day. And the capture rate or photographic rate of snow leopard was 1.53%. Meanwhile, 20 transects were run and 31 feces sample were collected. According to 32 photos, photographic rate and sign survey after snowing on the spot, were about 5-8 individuals of snow leopards in the research area, and the minimum density of snow leopard in Muzat Valley was 2.0 – 3.2 individuals/100 km2. We observed the behavior of ibex for 77.3 hours, and found about 20 groups and a total of approximately 264 ibexes in the research area.

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.