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Lovari, S., Minder, I., Ferretti, F., Mucci, N., Randi, E., Pellizzi, B. (2013). Common and snow leopards share prey, but not habitats: competition avoidance by large predators. Journal of Zoology, 291, 127–135.
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. |
Lovari, S., Ventimiglia, M., Minder, I. (2013). Food habits of two leopard species, competition, climate change and upper treeline: a way to the decrease of an endangered species? Ethology Ecology & Evolution, 25(4), 305–318.
Abstract: For carnivore species, spatial avoidance is one of the evolutionary solutions to
coexist in an area, especially if food habits overlap and body sizes tend to coincide. We reviewed the diets of two large cats of similar sizes, the endangered snow leopard (Panthera uncia, 16 studies) and the near-threatened common leopard (Panthera par- dus, 11 studies), in Asia. These cats share ca 10,000 km2 of their mountainous range, although snow leopards tend to occur at a significantly higher altitude than common leopards, the former being a cold-adapted species of open habitats, whereas the latter is an ecologically flexible one, with a preference for woodland. The spectrum of prey of common leopards was 2.5 times greater than that of snow leopards, with wild prey being the staple for both species. Livestock rarely contributed much to the diet. When the breadth of trophic niches was compared, overlap ranged from 0.83 (weight categories) to one (main food categories). As these leopard species have approximately the same size and comparable food habits, one can predict that competition will arise when they live in sympatry. On mountains, climate change has been elevating the upper forest limit, where both leopard species occur. This means a habitat increase for common leopards and a substantial habitat reduction for snow leopards, whose range is going to be squeezed between the forest and the barren rocky altitudes, with medium- to long-term undesirable effects on the conservation of this endangered cat |
Lui, C. -guang, Zheng, C. -wu, & Ren, J. -rang. (2003). Research Foods and Food Sources About Snow Leopard (Panthera uncia) (Vol. 31).
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. Keywords: research; foods; food; snow; snow leopard; snow-leopard; leopard; panthera; panthera uncia; Panthera-uncia; uncia; Chinese; deer; kiang; argali; Qinghai; gansu; Sichuan; Comparative; congruence; species; distribution; variation
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Mallon, D. P., Jackson, R. M. (2017). A downlist is not a demotion: Red List status and reality. Oryx, , 1–5.
Abstract: Assessments of biodiversity status are needed to
track trends, and the IUCN Red List has become the accepted global standard for documenting the extinction risk of species. Obtaining robust data on population size is an essential component of any assessment of a species� status, including assessments for the IUCN Red List. Obtaining such estimates is complicated by methodological and logistical issues, which are more pronounced in the case of cryptic species, such as the snow leopard Panthera uncia. Estimates of the total population size of this species have, to date, been based on little more than guesstimates, but a comprehensive summary of recent field research indicates that the conservation status of the snow leopard may be less dire than previously thought. A revised categorization, from Endangered to Vulnerable, on the IUCN Red List was proposed but met some opposition, as did a recent, similar recategorization of the giant panda Ailuropoda melanoleuca. Possible factors motivating such attitudes are discussed. Downlisting on the IUCN Red List indicates that the species concerned is further from extinction, and is always to be welcomed, whether resulting from successful conservation intervention or improved knowledge of status and trends. Celebrating success is important to reinforce the message that conservation works, and to incentivize donors. |
Manati, A. R. (2008). Fur trade of large cats and the question of the subspecies status of leopards in Afghanistan (Der Handel mit Fellen von Grosskatzen und die Abklärung der Unterartenfrage beim. Germany: University of Köln.
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. |
Marma, B. B., Yunchis, V.V. (1969). Biology of the snow leopard (Panthera uncia uncia). Zoologicheskii Zhurnal, 47(11), 1689–1694.
Abstract: The methods to obtain progeny of the snow-leopard (Panthera uncia uncia) in captivity were being elaborated in the zoological garden of Kaunas, Lithuanian SSR. The blood characteristics for snow-leopards is given and compared to that for African lions and Sumatran tigers. A series of internal, external and clinical indices is established. The rut lasts for 5-7 day, the duration of pregnancy equals 98 days. The duration of lactation varies from 3 to 4 months. Sexual maturity is attained on the 3rd-4th year. From 1960 to 1967 in zoological ghardens of the world abuot 29 snow-leopards were born. 14 of them -- in the Kauna zoological garden.
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Marma, B. B., & Yunchis, V. V. (1968). Observations on the breeding, management and physiology of Snow leopards (Panthera u. uncia) at Kaunas Zoo from 1962 to 1967. In C. Jarvis, & R. Biegler (Eds.), Canids and Felids in Captivity (pp. 66–73). Zoological Society of London. |
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. |
McCarthy, T. (2000). Ecology and Conservation of Snow Leopards, Gobi Brown Bears, and Wild Bactrian Camels in Mongolia. Ph.D. thesis, University of Massachusetts, Amherst, .
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.
Keywords: snow leopard; Uncia uncia; Mongolia; radio-collar; habitat use; movements; ecology; wild camel; brown bear; 5340
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McCarthy, T., Fuller, T., & Munkhtsog, B. (2005). Movements and activities of snow leopards in Southwestern Mongolia (Vol. 124).
Abstract: Four adult (2M:2F) snow leopards (Uncia uncia) were radio-monitored (VHF; one also via satellite) year-round during 1994-1997 in the Altai Mountains of southwestern Mongolia where prey densities (i.e., ibex, Capra siberica) were relatively low (0.9/km2). Marked animals were more active at night (51%) than during the day (35%). Within the study area, marked leopards showed strong a.nity for steep and rugged terrain, high use of areas rich in ungulate prey, and a.nity for habitat edges. The satellite-monitored leopard moved more than 12 km on 14% of consecutive days monitored. Home ranges determined by standard telemetry techniques overlapped substantially and were at least 13-141 km2in size. However, the satellite-monitored individual apparently ranged over an area of at least 1590 km2, and perhaps over as much as 4500 km2. Since telemetry attempts from the ground were
frequently unsuccessful dx¬ 72%_, we suspect all marked animals likely had large home ranges. Relatively low prey abundance in the area also suggested that home ranges of >500 km2were not unreasonable to expect, though these are >10-fold larger than measured in any other part of snow leopard range. Home ranges of snow leopards may be larger than we suspect in many areas, and thus estimation of snow leopard conservation status must rigorously consider logistical constraints inherent in telemetry studies, and the relative abundance of prey. Keywords: snow leopard; Uncia uncia; Mongolia; satellite radio-telemetry; home range; activity patterns; 6310
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