Abstract: Resource exploitation and behavioural interference underlie competition among
carnivores. Competition is reduced by specializing on different prey and/or spatiotemporal
separation, usually leading to different food habits. We predicted that
two closely related species of large cats, the endangered snow leopard and the
near-threatened common leopard, living in sympatry, would coexist through
habitat separation and exploitation of different prey species. In central Himalaya,
we assessed (2006–2010) habitat and diet overlap between these carnivores. The
snow leopard used grassland and shrubland, whereas the common leopard
selected forest. Contrary to our prediction, snow leopard and common leopard
preyed upon similar wild (Himalayan tahr, musk deer) and domestic species (Bos
spp., dogs). Dietary overlap between snow leopard and common leopard was 69%
(yearly), 76% (colder months) and 60% (warmer months). Thus, habitat separation
should be the result of other factors, most likely avoidance of interspecific
aggression. Habitat separation may not always lead to the use of different prey.
Avoidance of interspecific aggression, rather than exploitation of different
resources, could allow the coexistence of potentially competing large predators.

Abstract: During 1984-1987, 1992-1995, and 1998-2001, the author researched snow leopard, white lipped deer, kiang, and argali in Qinghai, Gansu, Xingiang, and Sichuan. He collected 644 snow leopard droppings, and analyzed kinds of foods and sources from perch. Snow leopard's foods include most main foods, main foods, comparative foods and lesser foods. Studied one another
index of faunistic congruence of foods species that from various distribution and variation both perch vertical variety and foods of snow leopard.

Abstract: Over a time of four years the bazars of Afghanistan were surveyed for furs of spotted wild cats, in particular leopards and snow leopards. In 2004 in Kabul a total of 28 furs of leopards were purchased by shopkeepers and 21 sold at an average price of 825 $. In the same year 25 furs of snow leopards were purchased and 19 sold to clients at an average price of 583 $. In 2006 at a single inspection double as many furs of leopards were found to be offered for sale in comparison to the whole year of 2004. Also prices had increased over the two years by 20 % to an average of 1037 $. Similarly the number of furs of snow leopards at 21 pieces was higher than in 2004, and the prices had increased to an average of 652 $. In 2007 investigations rendered more difficult, because the authorities had started to control the fur trade, and the results are not unequivocal. Clients were without any exception foreigners.
Surveys in 2004 in Mazar-e-Sharif, Kunduz, Takhar and Faiz Abad, in 2006 additionally in Baharak and Iskashem in the province of Badakhshan, revealed a regular trade in furs of spotted cats, however not as extensive as in Kabul. The most interesting finding was a fur of a cheetah in Mazar-e-Sharif, the first record of this species after 35 years.
From the surveys can be concluded that leopards still exist in the whole range of its distribution area in Afghanistan. However they don't allow any conclusion on the population size and its threat by hunting. In contrast to the leopard there exists a recent estimation of the population size of the snow leopard, saying that there are still 100 to 200 snow leopards living in Afghanistan. On the basis of these figures as well as the numbers of furs traded annually a Population and Habitat Viability Analysis was conducted. The result of this analysis is alarming. It has to be assumed that the snow leopard will be extinct in Afghanistan within the next ten years. To improve the protection of spotted cats in Afghanistan it needs both, a better implementation of the existing legislation as well as an awareness campaign among potential clients, i. e. foreigners living in Afghanistan.
The second part of this thesis deals with the question of subspecies of leopards in Afghanistan. Out of the 27 subspecies described four are believed to exist in Afghanistan. However, according to a molecularbiological revision of the species there occurs only one subspecies in Afghanistan, Panthera pardus saxicolor. To clarify the subspecies question various measures of furs had been taken in the bazars. The results revealed that the leopards in Afghanistan are the biggest of its species. However a further differentiation according to the area of origin within the country was not possible. Also the traditional differentiation on the basis of colours and patterns on the furs was not possible.
In contrast to the molecularbiological investigations published not only samples of zoo animals were available in this study but also samples from the wild. The own results confim that almost all leopards from Afghanistan and Iran belong to one and the same subspecies, P. p. saxicolor. Only in the most eastern part of Afghanistan, the Indian leopard, Panthera pardus fusca, can be found. The International Studbook for the Persian Leopard was analysed. The whole population derives from a few founder animals, which were imported in the midth fifties from Iran and in the late sixties from Afghanistan. To avoid inbreeding later on the Iranian and the Afghan lines were mixed. A female imported in 1968 from Kabul to Cologne is represented in each of the more than 100 today living animals.Mixing the two lines subsequently is justified by the genetic results of this study. Recently acquired animals from the Caucasus, however, should be tested genetically before integrating them into the zoo population.

Abstract: Snow leopard ecology, distribution and abundance in Mongolia were studied between 1993 and 1999. I placed VHF and satellite radio-collars on 4 snow leopards, 2 males and 2 females, to determine home ranges, habitat use, movements, and activity. Home ranges of snow leopards in Mongolia were substantially larger than reported elsewhere. Males ranged over 61 – 142 km2 and female 58 to 1,590 km2. Cats had crepuscular activity patterns with daily movements averaging 5.1 km. Intraspecific distances averaged 1.3 km for males to 7.8 km for males. Leopards selected moderately to very-broken habitat with slopes > 20o, in areas containing ibex. Leopard distribution and abundance was determined using sign surveys. Leopard range in Mongolia is approximately 103,000 km2 but cats are not uniformly distributed within that range. High-density areas include the eastern and central Transaltai Gobi and the northern Altai ranges. Relative leopard densities compared well with relative ibex densities on a regional basis. A snow leopard conservation plan was drafted for Mongolia that identifies problems and threats, and provides an action plan. Wild Bactrian camels occur in the Great Gobi National Park (GGNP) and are thought to be declining due to low recruitment. I surveyed camels by jeep and at oases, observing 142 (4.2% young) and 183 (5.3% young) in 1997 and 1998. Current range was estimated at 33,300 km2. Some winter and calving ranges were recently abandoned. Track sizes and tooth ages from skulls were used to assess demographics. A deterministic model was produced that predicts camel extinction within 25 to 50 years under current recruitment rates and population estimates. Gobi brown bears are endemic to Mongolia and may number less than 35. Three population isolates may occur. I collected genetic material from bears at oases using hair traps. Microsatellite analyses of nuclear DNA determined sixteen unique genotypes, only two of which occurred at more than one oases. Genetic diversity was very low with expected heterozygosity = 0.32, and alleles per locus = 2.3. Mitochondrial DNA sequences were compared to other clades of brown bear and found to fall outside of all known lineages.