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Bartlett, L. (1997). Good News for the Bad and the Ugly at CITES Conference.
Abstract: And prices can be high. CITES lists the following record payments (in US dollars): Falcon, 200,000; snow leopard skins, 60,000; musk grain, 50,000 per kilogramme; South American parrot, 40,000; Peruvian butterfly, 3,000; orchid, 2,000. Apparently rare creatures are worth the earth, to some people.
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Oli, M. K. (1993). A key for the identification of the hair of mammals of a snow leopard (Panthera uncia) habitat in Nepal. Journal of Zoology London, 231(1), 71–93.
Abstract: Analysis of prey remains in scats, particularly hairs, in widely used to study diet of mammalian predators, but identification of hair is often difficult because hair structures vary considerably both within and between species. Use of photographic reference of diagnostically important hair structures from mammals occurring in a predator's habitat has been found to be convenient for routine identification. A photographic reference key was developed for the identification of hairs of the mammals known to occur in a snow leopard (Panthera uncia) habitat in the Annapurna Conservation Area, Nepal. The key included a photographic reference of the diagnostic hair structures of nine species of wild and five species of domestic mammals. The cross-sectional appearance, shape and arrangement of medulla, the ratio of cortex to medulla, and the form and distribution of pigment in medulla and cortex were important diagnostic aids in the identification of hairs.
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Abzalov A.A. (1974). Game management development.
Abstract: An issue of wildlife conservation in game preserves, forestries, and sanctuaries is discussed. In some regions of Uzbekistan there are various protected wildlife areas preserving unique and game species: marchor in the Kugitan hunting farm, Bukhara deer the Bukhara region, bear and snow leopard, argali, ibex, wild-boars, snow-cock, partridge, eagle, etc. in the Miraki hunting farm, pheasants in the Karadara forestry. To restore and upgrade the game management level in the country it is required to properly create game preserves, enlarge reproduction activity, strictly follow rules and terms of hunting and cultivate careful and solicitous attitude to wildlife and its resources in all hunters.
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Suryawanshi, K. R., Redpath, S. M., Bhatnagar, Y. V., Ramakrishnan, U., Chaturvedi, V., Smout, S. C., Mishra, C. Impact of wild prey availability on livestock predation by snow leopards. Royal Society Open Science, , 1–11.
Abstract: An increasing proportion of the world�s poor is rearing livestock today, and the global livestock population is growing. Livestock predation by large carnivores and their retaliatory
killing is becoming an economic and conservation concern. A common recommendation for carnivore conservation and for reducing predation on livestock is to increase wild prey populations based on the assumption that the carnivores will consume this alternative food. Livestock predation, however, could either reduce or intensify with increases in wild prey depending on prey choice and trends in carnivore abundance. We show that the extent of livestock predation by the endangered snow leopard Panthera uncia
intensifies with increases in the density of wild ungulate prey, and subsequently stabilizes. We found that snow leopard density, estimated at seven sites, was a positive linear function of the density of wild ungulates�the preferred prey�and showed no discernible relationship with livestock density. We also found that modelled livestock predation increased with livestock density. Our results suggest that snow leopard conservation would benefit from an increase in wild ungulates, but that would intensify the problem of livestock predation for pastoralists. The potential benefits of increased wild prey abundance in reducing livestock predation
can be overwhelmed by a resultant increase in snow leopard populations. Snow leopard conservation efforts aimed atfacilitating increases in wild prey must be accompanied by greater assistance for better livestock
protection and offsetting the economic damage caused by carnivores.
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Suryawanshi, K. R., Redpath, S., Bhatnagar, Y. V., Ramakrishnan, U., Chaturvedi, V., Smout, S. C., Mishra, C. (2017). Impact of wild prey availability on livestock predation by snow leopards. Royal Society Open Science, , 1–11.
Abstract: An increasing proportion of the world�s poor is rearing
livestock today, and the global livestock population is growing.
Livestock predation by large carnivores and their retaliatory
killing is becoming an economic and conservation concern.
A common recommendation for carnivore conservation and
for reducing predation on livestock is to increase wild prey
populations based on the assumption that the carnivores
will consume this alternative food. Livestock predation,
however, could either reduce or intensify with increases
in wild prey depending on prey choice and trends in
carnivore abundance. We show that the extent of livestock
predation by the endangered snow leopard Panthera uncia
intensifies with increases in the density of wild ungulate
prey, and subsequently stabilizes. We found that snow leopard
density, estimated at seven sites, was a positive linear
function of the density of wild ungulates�the preferred
prey�and showed no discernible relationship with livestock
density. We also found that modelled livestock predation
increased with livestock density. Our results suggest that
snow leopard conservation would benefit from an increase
in wild ungulates, but that would intensify the problem of
livestock predation for pastoralists. The potential benefits of
increased wild prey abundance in reducing livestock predation
can be overwhelmed by a resultant increase in snow leopard
populations. Snow leopard conservation efforts aimed at
facilitating increases in wild prey must be accompanied by greater assistance for better livestock
protection and offsetting the economic damage caused by carnivores.
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Gromov I.M. (1963). Felis (Uncia) uncia Schreber (1776) leopard or irbis (Vol. Part.2.).
Abstract: An identification table for genus and species of mammals of USSR is given. The taxonomy, morphology, distribution and life history are described. The features of snow leopard Felis (Uncia) uncia, distribution, biology and practical value are described.
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Aristov A.A. (2001). Genus Irbises Uncia Gray, 1854. Irbis or snow leopard Uncia uncia (Schreber, 1775).
Abstract: An identification table for genus and species of mammals of Russia and adjacent areas is given. The taxonomy, morphology, distribution and life history of carnivores are described. The features of genus Uncia and species Uncia uncia, geographical variability, distribution, biology and value are described in detail.
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Kuznetsov B.A. (1975). The cats – Felidae (Vol. Part 3.).
Abstract: An identification table for genus and species of Felidae family of USSR is given. Snow leopard Panthera uncia (Schreher) described for Pamir, Tien Shan, Altai and mountains of Tuva.
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Laptev M.K. (1936). The cats – Felidae (Vol. Issue V.).
Abstract: An identification table for genus and species of Felidae family of Turkmenistan is given. The following features are used: colour, pattern, teeth formula, skull measurements, and sizes of body, head, and tail. The presence of snow leopard for Kopet-Dag is indicated.
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Graham, L. H., Goodrowe, K. L., Raeside, J. I., & Liptrap, R. M. (1995). Non-invasive monitoring of ovarian function in several felid species by measurement of fecal estradiol-17-beta and progestins. Zoo Biology, 14(3), 223–237.
Abstract: An extraction and assay procedure to measure fecal estradiol-17-beta and progestin concentrations in several cat species was developed and validated for use for noninvasive monitoring of ovarian function. Fecal samples were collected over a range of 3-20 months from female tigers (three), lions (three), snow leopards (three), cheetahs (two), caracals (two), and domestic cats (five). Samples were extracted with 90% methanol, lipids removed with petroleum ether, and the estradiol and progestins in the methanol measured by radioimmunoassay (RIA). High Performance Liquid Chromatography (HPLC) fractionation and subsequent RIA of the fractions indicated that the estradiol-17-beta antiserum cross-reacted primarily with estradiol-17-beta in the feces of lions and tigers and was assumed to be specific for estradiol-17-beta in the feces of other species as well. However, there were several immunoreactive compounds, presumably progesterone metabolites, excreted in the feces which varied both quantitatively and qualitatively among species. The behavior of tigers, lions, cheetahs, and caracals was visually monitored during the collection period and frequency of sexual behaviors was positively correlated with increases in fecal estradiol in all species observed. The mean fecal estradiol-17-beta peaks were as follows: tigers, 128.0 +- 13.1; lions, 186.0 +- 14.8; snow leopards, 136.7 +- 15.9; cheetahs, 140.9 +- 9.0; caracals, 24.5 +- 4.0; and domestic cats 158.9 +- 19.3 ng/gm. Fecal progestin concentrations rose significantly (P lt 0,001) only after breeding or during pregnancy and were as follows: tigers, 5.6 +- 0.6; lions, 1.9 +- 0.1; cheetahs, 8.4 +- 1.1; and caracals, 2.4 +- 0.4 mu-g/gm. Fecal progestins were elevated for one-half to two-thirds of the gestation length during presumed pseudopregnancy but remained elevated throughout successful pregnancies. These results suggest that ovarian function can be monitored noninvasively in the family Felidae by the measurement of fecal estradiol-17-beta and progestin concentrations.
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