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Rana, B. S. (1997). Distinguishing kills of two large mammalian predators in Spiti Valley Himachal Pradesh. J.Bombay Nat.Hist.Soc, 94(3), 553.
Abstract: The author studied livestock killed by predators in the Spiti Valley, India, to determine what species had killed yaks, horses, donkeys, and other domestic animals. Eleven of the kills examined were made by snow leopards and six by the Tibetan wolf. Wolves were involved in surplus killings, while snow leopards kill as food is needed. lgh
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Reed-Smith, J., & Kumpf, M. (1998). Snow leopards (Uncia uncia): family group management alternatives. Anim.Keepers' Forum, 25(10), 386–391.
Abstract: The authors offer insights into creating family groups of snow leopards in zoos. The programs at the Denver Zoo, Denver, Colorado, and at John Ball Zoological Gardens, Grand Rapids, Michigan, are highlighted. lgh.
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Shafiq, M. M., & Abid, A. (1998). Status of large mammal species in Khunjerab National Park. Pakistan Journal of Forestry, 48(1-4), 91–96.
Abstract: Study on the current status of large mammals species population was carried out in Khunjerab National Park, Northern Areas. The observation recorded showed that the population of Tibetan Red fox (Vulpes vulpes montana), Snow leopard (Uncia uncia), and Wolf (Canis lupus) have, though a bit, increased but are still in the rank of “Endangered”. While the population of Himalyan Ibex (Cpara ibex sibirica) is increasing more rapidly and their status is now “Common” in the Park. The limited population of Marcopolo sheep (Ovis ammon polii), Tibetan wild Ass (Equus hemionus kiang) and Brown bear (Urus arctos) is still under threat, and comes them under “Critical Endangered” category.
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Shi, K., Jun, Z. F. S., Zhigang, D., Riordan, P., & MacDonald, D. (2009). Reconfirmation of snow leopards in Taxkurgan Nature Reserve, Xinjiang, China. Oryx, 43(2), 169–170.
Abstract: China may hold a greater proportion of the global snow leopard Panthera uncia population than any other country, with the area of good quality suitable habitat, estimated at nearly 300,000 km2, comprising .50% of that available across the species' entire range. We can now reconfirm the presence of snow leopard in the Taxkurgan area of Xinjiang Province in north-west China after a period of 20 years.
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Shrestha, B. (2008). Prey Abundance and Prey Selection by Snow Leopard (uncia uncia) in the Sagarmatha (Mt. Everest) National Park, Nepal.
Abstract: Predators have significant ecological impacts on the region's prey-predator dynamic and community structure through their numbers and prey selection. During April-December 2007, I conducted a research in Sagarmatha (Mt. Everest) National Park (SNP) to: i) explore population status and density of wild prey species; Himalayan tahr, musk deer and game birds, ii) investigate diet of the snow leopard and to estimate prey selection by snow leopard, iii) identify the pattern of livestock depredation by snow leopard, its mitigation, and raise awareness through outreach program, and identify the challenge and opportunities on conservation snow leopard and its co-existence with wild ungulates and the human using the areas of the SNP. Methodology of my research included vantage points and regular monitoring from trails for Himalayan tahr, fixed line transect with belt drive method for musk deer and game birds, and microscopic hair identification in snow leopard's scat to investigate diet of snow leopard and to estimate prey selection. Based on available evidence and witness accounts of snow leopard attack on livestock, the patterns of livestock depredation were assessed. I obtained 201 sighting of Himalayan tahr (1760 individuals) and estimated 293 populations in post-parturient period (April-June), 394 in birth period (July -October) and 195 November- December) in rutting period. In average, ratio of male to females was ranged from 0.34 to 0.79 and ratio of kid to female was 0.21-0.35, and yearling to kid was 0.21- 0.47. The encounter rate for musk deer was 1.06 and density was 17.28/km2. For Himalayan monal, the encounter rate was 2.14 and density was 35.66/km2. I obtained 12 sighting of snow cock comprising 69 individual in Gokyo. The ratio of male to female was 1.18 and young to female was 2.18. Twelve species (8 species of wild and 4 species of domestic livestock) were identified in the 120 snow leopard scats examined. In average, snow leopard predated most frequently on Himalayan tahr and it was detected in 26.5% relative frequency of occurrence while occurred in 36.66% of all scats, then it was followed by musk deer (19.87%), yak (12.65%), cow (12.04%), dog (10.24%), unidentified mammal (3.61%), woolly hare (3.01%), rat sp. (2.4%), unidentified bird sp. (1.8%), pika (1.2%), and shrew (0.6%) (Table 5.8 ). Wild species were present in 58.99% of scats whereas domestic livestock with dog were present in 40.95% of scats. Snow leopard predated most frequently on wildlife species in three seasons; spring (61.62%), autumn (61.11%) and winter (65.51%), and most frequently on domestic species including dog in summer season (54.54%). In term of relative biomass consumed, in average, Himalayan tahr was the most important prey species contributed 26.27% of the biomass consumed. This was followed by yak (22.13%), cow (21.06%), musk deer (11.32%), horse (10.53%), wooly hare (1.09%), rat (0.29%), pika (0.14%) and shrew (0.07%). In average, domestic livestock including dog were contributed more biomass in the diet of snow leopard comprising 60.8% of the biomass consumed whilst the wild life species comprising 39.19%. The annual prey consumption by a snow leopard (based on 2 kg/day) was estimated to be three Himalayan tahr, seven musk deer, five wooly hare, four rat sp., two pika, one shrew and four livestock. In the present study, the highest frequency of attack was found during April to June and lowest to July to November. The day of rainy and cloudy was the more vulnerable to livestock depredation. Snow leopard attacks occurred were the highest at near escape cover such as shrub land and cliff. Both predation pressure on tahr and that on livestock suggest that the development of effective conservation strategies for two threatened species (predator and prey) depends on resolving conflicts between people and predators. Recently, direct control of free – ranging livestock, good husbandry and compensation to shepherds may reduce snow leopard – human conflict. In long term solution, the reintroduction of blue sheep at the higher altitudes could also “buffer” predation on livestock.
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Sloane, A., Kelly, C., McDavitt, S., & Marples, N. (1998). Big cats in captivity: a quantitative analysis of enrichment. Adv.Etho, 33, 43.
Abstract: Studies on three species of big cats at Dublin Zoo have led to firm conclusions about the effects of certain forms of enrichment, some of which will be presented here. Lions, jaguars, and snow leopards were studied over two years and their behaviours quantified using focal animal sampling during selected hours during daylight. By comparison of these activity budgets with and without the enrichments being present, it was possible to identify the exact behavioural changes caused by each enrichment method, and to quantify these changes. In this contribution we present results showing that the presence of a platform in both lion and jaguar enclosures dramatically reduced stereotypic pacing behaviour. We will demonstrate that the effects of short term enrichment devices may have a wide range of effects on behaviours which outlast the presence of the stimulus. For instance scents added to the cage, or food/play items such as horse hides, hidden fish or ice-blocks often reduce pacing and increase resting later in the day, even after the cats have ceased using the enrichment items. This reduction in pacing and increase in resting time often meant that the amount of the enclosure used per hour was actually reduced with the presence of new stimuli, as result opposite to what might have been expected. The results of these studies will be discussed in relation to effective animal management.
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Smith, A. T., & Foggin, M. J. (1998). The Plateau Pika (Ochotona curzoniae) is a Keystone Species for Biodiversity on the Tibetan Plateau. Animal Conservation, 2, 235–240.
Abstract: It is necessary to look at the big picture when managing biological resources on the QinghaiXizang (Tibetan) plateau. Plateau pikas (Ochotona curzoniae) are poisoned widely across the plateau. Putative reasons for these control measures are that pika populations may reach high densities and correspondingly reduce forage for domestic livestock (yak, sheep, horses), and because they may be responsible for habitat degradation. In contrast, we highlight the important role the plateau pika plays as a keystone species in the Tibetan plateau ecosystem. The plateau pika is a keystone species because it: (i) makes burrows that are the primary homes to a wide variety of small birds and lizards; (ii) creates microhabitat disturbance that results in an increase in plant species richness; (iii) serves as the principal prey for nearly all of the plateau's predator species; (iv) contributes positively to ecosystem-level dynamics. The plateau pika should be managed in concert with other uses of the land to ensure preservation of China's native biodiversity, as well as long-term sustainable use of the pastureland by domestic livestock.
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Suryawanshi, K. R., Bhatnagar, Y., & Mishra, C. (2009). Why should a grazer browse? Livestock impact on winter resource use by bharal Pseudois nayaur
. Oecologia, , 1–10.
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.
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Suryawanshi, K. R. (2009). Towards snow leopard prey recovery: understanding the resource use strategies and demographic responses of bharal Pseudois nayaur to livestock grazing and removal; Final project report.
Abstract: Decline of wild prey populations in the Himalayan region, largely due to competition with livestock, has been identified as one of the main threats to the snow leopard Uncia uncia. Studies show that bharal Pseudois nayaur diet is dominated by graminoids during summer, but the proportion of graminoids declines in winter. We explore the causes for the decline of graminoids from bharal winter diet and resulting implications for bharal conservation. We test the predictions generated by two alternative hypotheses, (H1) low graminoid availability caused by livestock grazing during winter causes bharal to include browse in their diet, and, (H2) bharal include browse, with relatively higher nutrition, to compensate for the poor quality of graminoids during winter. Graminoid availability was highest in areas without livestock grazing, followed by areas with moderate and intense livestock grazing. Graminoid quality in winter was relatively lower than that of browse, but the difference was not statistically significant. Bharal diet was dominated by graminoids in areas with highest graminoid availability. Graminoid contribution to bharal diet declined monotonically with a decline in graminoid availability. Bharal young to female ratio was three times higher in areas with high graminoid availability than areas with low graminoid availability. No starvation-related adult mortalities were observed in any of the areas. Composition of bharal winter diet was governed predominantly by the availability of graminoids in the rangelands. Since livestock grazing reduces graminoid availability, creation of livestock free areas is necessary for conservation of grazing species such as the bharal and its predators such as the endangered snow leopard in the Trans-Himalaya.
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The Snow Leopard Conservancy. (2002). Visitor Satisfaction and Opportunity Survey, Manang, Nepal: Market Opportunities for Linking Community-Based Ecotourism with the Conservation of Snow Leopards in the Annpurna Conservation Area. Report prepared for WWF-Nepal Programme (Vol. SLC Field Document Series No 3).
Abstract: For the past two decades, the Manang or Nyeshang Valley has become one of the most popular
trekking routes in Nepal, attracting over 15,000 trekkers annually (Ale, 2001). The 21-day
circular trek takes the visitor from the lush southern slopes of the Annapurna massif around to
its dry northern slopes more reminiscent of Tibet, through a landscape of spectacular mountain
scenes, interesting villages and diverse cultures. The Manang region also offers prime habitat
for the endangered snow leopard, supporting an estimated 4.8 – 6.7 snow leopards per 100 sq.
km (Oli 1992). This high density has been attributed to the abundance of blue sheep, the snow
leopard's primary large prey species across the Himalayan Mountains and Tibetan Plateau.
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ud Din, J. (2008). Assessing the Status of Snow Leopard in Torkhow Valley, District Chitral, Pakistan: Final Technical Report.
Abstract: This study was aimed at assessing the status of Snow leopard, its major prey base, and the extent of human-Snow leopard conflict and major threats to the wildlife in north Chitral (Torkhow valley) Pakistan. Snow leopard occurrence was conformed through sign transect surveys i.e. SLIMS. Based on the data collected the number of Snow leopards in this survey block (1022 Kmý) is estimated to be 2-3 animals. Comparing this estimate with the available data from other parts of the district the population of snow leopard in Chitral district was count to be 36 animals. Livestock depredation reports collected from the area reflect the existence of human-snow leopard conflict and 138 cases were recorded affecting 102 families (in a period of eight years, 2001-2008). Ungulates (Himalayan Ibex) rut season surveys were conducted in coordination with NWFP Wildlife department. A total of 429 animals were counted using direct count (point method) surveys. Other snow leopard prey species recorded include marmot, hare, and game birds. Signs of other carnivores i.e. wolf, jackal, and fox were also noticed. Major threats to the survival of wildlife especially snow leopard reckoned include retaliatory killing (Shooting, Poisoning), poaching, loss of natural prey, habitat degradation (over grazing, fodder and fuel wood collection), lack of awareness, and over population. GIS map of the study area was developed highlighting the area searched for Snow leopard and its prey species. Capacity of the Wildlife Department staff was built in conducting SLIMS and ungulate surveys through class room and on field training. Awareness regarding the importance of wildlife conservation was highlighted to the students, teachers and general community through lectures and distribution of resource materials developed by WWF-Pakistan.
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Vashetko, E., Esipov A., Bykova, E., & Kreuzberg, E. (2005). Snow Leopard Bibliography. Central Asia (Abstracts).
Abstract: Bibliography of the Snow Leopard included publications on the studying various questions of ecology and conservation of the Snow Leopard in Central Asia (305) for the period 1873 to 2004. The most important works on this species in the region, as well as results of the analysis of timing of publications was described.
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Wharton, D. (1997). Endangered Species Update. Endangered Species Update, 14(11), 13.
Abstract: The snow leopard is listed as endangered, although most of its high mountain habitat remains untouched. However the ability of humans to exploit wildlife has led to it being endangered. Serious attempts to keep snow leopards in captivity began in 1891, but it was not until the 1950s that cubs survived long enough to become breeders. The American Zoo and Aquarium Association (ASA) Snow Leopard Species Survival Plan (SSP) was set up in 1984, achieving success with breeding goals.
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Ying-xiang, W. (2003). A complete checklist of mammal species and subspecies in China, a taxonomic and geographic reference. Beijing: China Forestry Publishing House.
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Zhang, F., Jiang, Z., Zeng, Y., & McCarthy, T. (2007). Development of primers to characterize the mitochondrial control region of the snow leopard (Uncia uncia) (Vol. 7).
Abstract: The snow leopard (Uncia uncia) is a rare carnivore living above the snow line in central Asia. Using universal primers for the mitochondrial genome control region hypervariable
region 1 (HVR1), we isolated a 411-bp fragment of HVR1 and then designed specific primers
near each end of this sequence in the conserved regions. These primers were shown to yield
good polymerase chain reaction products and to be species specific. Of the 12 snow leopards
studied, there were 11 segregating sites and six haplotypes. An identification case of snow
leopard carcass (confiscated by the police) proved the primers to be a useful tool for forensic
diagnosis in field and population genetics studies.
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Korablev, M. P., Poyarkov, A. D., Karnaukhov, A. S., Zvychaynaya, E. Y., Kuksin, A. N., Malykh, S. V., Istomov, S. V., Spitsyn, S. V., Aleksandrov, D. Y., Hernandez-Blanco, J. A., Munkhtsog, B., Munkhtogtokh, O., Putintsev, N. I., Vereshchagin, A. S., Becmurody, A., Afzunov, S., Rozhnov, V. V. (2021). Large-scale and fine-grain population structure and genetic diversity of snow leopards (Panthera uncia Schreber, 1776) from the northern and western parts of the range with an emphasis on the Russian population. Conservation Genetics, .
Abstract: The snow leopard (Panthera uncia Schreber, 1776) population in Russia and Mongolia is situated at the northern edge of the range, where instability of ecological conditions and of prey availability may serve as prerequisites for demographic instability and, consequently, for reducing the genetic diversity. Moreover, this northern area of the species distribution is connected with the western and central parts by only a few small fragments of potential habitats in the Tian-Shan spurs in China and Kazakhstan. Given this structure of the range, the restriction of gene flow between the northern and other regions of snow leopard distribution can be expected. Under these conditions, data on population genetics would be extremely important for assessment of genetic diversity, population structure and gene flow both at regional and large-scale level. To investigate large-scale and fine-grain population structure and levels of genetic diversity we analyzed 108 snow leopards identified from noninvasively collected scat samples from Russia and Mongolia (the northern part of the range) as well as from Kyrgyzstan and Tajikistan (the western part of the range) using panel of eight polymorphic microsatellites. We found low to moderate levels of genetic diversity in the studied populations. Among local habitats, the highest heterozygosity and allelic richness were recorded in Kyrgyzstan (He = 0.66 ± 0.03, Ho = 0.70 ± 0.04, Ar = 3.17) whereas the lowest diversity was found in a periphery subpopulation in Buryatia Republic of Russia (He = 0.41 ± 0.12, Ho = 0.29 ± 0.05, Ar = 2.33). In general, snow leopards from the western range exhibit greater genetic diversity (He = 0.68 ± 0.04, Ho = 0.66 ± 0.03, Ar = 4.95) compared to those from the northern range (He = 0.60 ± 0.06, Ho = 0.49 ± 0.02, Ar = 4.45). In addition, we have identified signs of fragmentation in the northern habitat, which have led to significant genetic divergence between subpopulations in Russia. Multiple analyses of genetic structure support considerable genetic differentiation between the northern and western range parts, which may testify to subspecies subdivision of snow leopards from these regions. The observed patterns of genetic structure are evidence for delineation of several management units within the studied populations, requiring individual approaches for conservation initiatives, particularly related to translocation events. The causes for the revealed patterns of genetic structure and levels of genetic diversity are discussed.
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Atzeni, L., Cushman, S. A., Bai, D., Wang, J., Chen, P., Shi,
K., Riordan, P. (2020). Meta-replication, sampling bias, and multi-scale model selection:
A case study on snow leopard (Panthera uncia) in western China. Ecology and Evolution, , 1–27.
Abstract: Replicated multiple scale species distribution models (SDMs)
have become increasingly important to identify the correct variables
determining species distribution and their influences on ecological
responses. This study explores multi-scale habitat relationships of the
snow leopard (Panthera uncia) in two study areas on the Qinghai–Tibetan
Plateau of western China. Our primary objectives were to evaluate the
degree to which snow leopard habitat relationships, expressed by
predictors, scales of response, and magnitude of effects, were
consistent across study areas or locally landcape-specific. We coupled
univariate scale optimization and the maximum entropy algorithm to
produce multivariate SDMs, inferring the relative suitability for the
species by ensembling top performing models. We optimized the SDMs based
on average omission rate across the top models and ensembles’ overlap
with a simulated reference model. Comparison of SDMs in the two study
areas highlighted landscape-specific responses to limiting factors.
These were dependent on the effects of the hydrological network,
anthropogenic features, topographic complexity, and the heterogeneity of
the landcover patch mosaic. Overall, even accounting for specific local
differences, we found general landscape attributes associated with snow
leopard ecological requirements, consisting of a positive association
with uplands and ridges, aggregated low-contrast landscapes, and large
extents of grassy and herbaceous vegetation. As a means to evaluate the
performance of two bias correction methods, we explored their effects on
three datasets showing a range of bias intensities. The performance of
corrections depends on the bias intensity; however, density kernels
offered a reliable correction strategy under all circumstances. This
study reveals the multi-scale response of snow leopards to environmental
attributes and confirms the role of meta-replicated study designs for
the identification of spatially varying limiting factors. Furthermore,
this study makes important contributions to the ongoing discussion about
the best approaches for sampling bias correction.
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(1978). Rare Animals and their Protection in the USSR.
Abstract: It described categories of threat (Category A and Category B). Snow leopard was assessed under Category A the species whose numbers and habitats have sharply diminished and are continuing to diminish as a consequence of direct persecution, destruction of their habitat or other causes. The snow leopard (Pardus uncia) inhabits the mountains of the Tien Shan range, Tarbagatai, Saur, Altai and the Sayans. Exploitation of mountain areas and depletion of stocks of wild ungulates (Siberian mountain goats and wild sheep) have led to a sharp reduction in the number of snow leopards. It is estimated that today only about one thousand leopards are left, and they have accordingly been placed under complete protection. Hunting and selective shooting are everywhere prohibited. Catching leopards is regulated by the articles of the international convention restricting trade in rare species of plants and animals.
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(1998). Biological diversity conservation. National strategy and action plan of the Republic of Uzbekistan.
Abstract: The National strategy and action plan of the Republic of Uzbekistan was signed on April 1, 1998. Snow leopard was included in the list of rare and endangered animal species and referred to category 2 a rare, not endangered species. It is distributed in highlands of the West Tien Shan and Pamiro-Alay. Its population is 30-50 animals. Snow leopard is protected in the Chatkal, Gissar nature reserve, and Ugam-Chatkal national park.
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Abdulnazarov A.G. (2002). About status of the Red Book vertebrates in the Zorkul nature reserve.
Abstract: In the nature reserve, there are 18 animal species listed in the Red Book of the Republic of Tajikistan including 8 mammal species, one of which, snow leopard, is in the Red List of IUCN. There are 10 Red Book bird species in the nature reserve. Pamir argali is represented by several dozens of isolated groups. No encounters of Tien Shan brown bear, dhole and lynx have been reported in the nature reserve over the last years. A total number of mountain geese were about 400, in the year 2001. Mongolian saker falcon was met twice. Two golden eagles and six lammergeyers were found too.
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Abdunazarov B.B. (1994). Rare and endangered animal species in the Kashkadaraya region.
Abstract: 41 percent of all vertebrate species listed in the Red Book of the Uzbek SSR (18 mammal species, 29 bird, 6 reptile, and 8 fish species) inhabit the Kashkadarya region. The mammals are Tien Shan brown bear, Central Asian otter, Turkistan lynx, snow leopard, and goitered gazelle. Nesting bird fauna includes the following species: black stork, Turkistan white stork, short toed eagle, booted eagle, golden eagle, bearded vulture, black vulture, griffon vulture, saker falcon, houbara bustard, and eagle owl. Migrating and wintering bird species are dalmatian pelican, rose pelican, mute swan, osprey, tawny eagle, imperial eagle, pin-tailed sandgrouse; and possibly Bonnli's eagle and Barbary falcon that have not been seen here since 1950-s. Rare reptiles are represented by two species: desert monitor and Central Asian cobra.
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Abdunazarov B.B. (1990). Composition, structure and population of rare terrene vertebrate animals and their conservation perspectives in the nature reserves of Uzbekistan.
Abstract: An attempt of analyzing the role of Uzbekistan' nature reserves in conservation of gene pool of the rare and endangered terrene vertebrate fauna is done. Of 21 rare vertebrate species, 11 mammal species, eight nesting bird species and two reptile species were detected to inhabit seven nature reserves. This makes up 36.2 percent within the total number of species included in the Red Data Book of the Uzbek SSR or 3.7 percent of the country's fauna. Single snow leopards were found in the Chatkal and Hissar nature reserves. Data of the species inhabiting the Zaamin nature reserve needs to be verified.
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Abdusalamov I.A. (2001). Required protection measures for rare and endangered vertebrate species in Tajikistan (Vol. N 2 (143)).
Abstract: The network of Tajikistan's protected areas (four nature reserves, 14 national and 18 regional sanctuaries, one national park) is described. The establishment of `Shakhristan state complex nature reserve' and `Sarykamish state complex reserve', and interstate nature complex park on northern slope of the Turkestan ridge is recommended to improve conservation practices for a number of endangered vertebrate animal species in Northern Tajikistan (such as brown bear, snow leopard, wild sheep, and others).
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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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Ale S. (2005). Have snow leopards made a comeback to the Everest region of Nepal?.
Abstract: In the 1960s, the endangered snow leopard was locally extirpated from the Sagarmatha (Mt. Everest) region of Nepal. In this Sherpa-inhabited high Himalaya, the flourishing tourism since the ascent of Mt Everest in 1953, has caused both prosperity and adverse impacts, the concern that catalyzed the establishment of Mt. Everest National Park in the region in 1976. In the late 1980s, there were reports that some transient snow leopards may have visited the area from adjoining Tibet, but no biological surveys exist to confirm the status of the cats and their prey. Have snow leopards finally returned to the top of the world? Exploring this question was the main purpose of this research project. We systematically walked altogether 24 sign transects covering over 13 km in length in three valleys, i.e. Namche, Phortse and Gokyo, of the park, and counted several snow leopard signs. The results indicated that snow leopards have made a comeback in the park in response to decades of protective measures, the virtual cessation of hunting and the recovery of the Himalayan tahr which is snow leopard's prey. The average sign density (4.2 signs/km and 2.5 sign sites/km) was comparable to that reported from other parts of the cats' range in the Himalaya. On this basis, we estimated the cat density in the Everest region between 1 to 3 cats per 100 sq km, a figure that was supported by different sets of pugmarks and actual sightings of snow leopards in the 60 km2 sample survey area. In the study area, tahr population had a low reproductive rate (e.g. kids-to-females ratio, 0.1, in Namche). Since predators can influence the size and the structure of prey species populations through mortality and through non-lethal effects or predation risk, snow leopards could have been the cause of the population dynamics of tahr in Sagarmtha, but this study could not confirm this speculation for which further probing may be required.
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