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Vyrypaev V.A. (1974). The influence of sarcoptosis on the population of Capra sibirica Pall. in Western Tien Shan (Vol. Vol. II.).
Abstract: Given is data concerning disease (sarcoptosis) of Siberian ibex (Capra sibirica) in Western Tien Shan. The carriers of the disease are adult males of Capra sibirica during distant migrations that as a rule take place in anticipation of snowy winters or owing to human influence. Ibexes are not merely infected with sarcoptosis but perish enmasse from the disease. In the first year the disease strikes down, in the main, migrants – adult males. Predators including snow leopard kill the weakened animals. During the recent five years the density of Carpa sibirica at the Chatkal Mountain-Forest Reservation dropped 2.3-fold as a result of sarcoptosis and owing to the migrations caused by the reduction of the population. Is recommended: 1. Stringent veterinary control at places of possible contacts between infected domestic animals and healthy wild ungulates. 2. Using modern technology migration routes of ungulates should be studied for elaborating effective measures of quarantine.
Keywords: Uzbekistan; Western Tien Shan; Chatkal nature reserve; sarcoptosis; predators; snow leopard.; 8560; Russian
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McCarthy, K., Fuller, T., Ming, M., McCarthy, T., Waits, L., & Jumabaev, K. (2008). Assessing Estimators of Snow Leopard Abundance (Vol. 72).
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. |