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Salles, L. O. (1992). Felid phylogenetics: Extant taxa and skull morphology (Felidae, Aeluroidae). American Museum Novitates, (3047), 1–67.
Abstract: relationships among extant felid taxa are controversial. A historical appraisal addresses component congruence among statements on felid phylogenetic relationships, and monophyly of generic ranks proposed for felids is discussed. Felid cranial morphology (especially the masticatory apparatus, basicranium, and rostral regions) is examined, and 44 characters are postulated for 39 taxa. Internal congruence for these characters is evaluated and 27 components are suggested. Parsimony analysis, using the successive weighting option of Hennig86, of the 44 cranial characters plus 13 other morphological features yields 29 components in a “modified Nelson” consensus cladogram. Two basal, well resolved clades are hypothesized in the total morphology analysis; under parenthetical notation the first is: (Hepailurus yagouaroundi (Puma concolor (Acinonyx jubatus (Uncia uncia (Neofelis nebulosa (Panthera tigris (P. onca, P. leo, and P. pardus)))))). The second clade is: Profelis temmincki (P. badia (Pardofelis marmorata ((Caracal caracal (Lynx rufus (L. lynx (L. pardina (L. canadensis)))) (Felis chaus (F. lybica (L. cafra (L. silvestris (F. bieti (F. nigripes (F. margarita (Octocolobus manul)))))))). Prionailurus planiceps and P. viverrina formed another group which is suggested as the basal branch of the felid phylogeny. The results in this study do not support monophyly of Leopardus Gray, 1841; Profelis Severtzon, 1858; and Prionailurus Severtzon, 1858. A better supported, more highly resolved, felid phylogenetic tree is needed.
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Saparbayev, S.K., & Woodward, D. B. (2008). Snow Leopard (Uncia uncia) as an Indicator Species and Increasing Recreation Loads in the Almaty Nature Reserve.
Abstract: The purpose of this research is to analyze the data on ecology, biology and dynamics of snow leopard population in the Almaty Nature Reserve and to identify if the increasing numbers of ecotourists could contribute to the decrease of Uncia uncia population. The results of the study show that increasing recreation loads in the Reserve and adjacent territories elevate the disturbance level to the snow leopard's main prey Siberian Ibex and to the predator itself that could result in a decrease of population of this endangered species or its total extinction.
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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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Sumiya, G., Buyantsog, B., & WWF Mongolia Country Office. (2002). Conservation of Snow Leopard in the Turgen and Tsagaan Shuvuut Mountains Through Local Involvement.. Islt: Islt.
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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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Wei, L., Wu, X., & Jiang, Z. (2008). The complete mitochondrial genome structure of snow leopard Panthera uncia.
Abstract: The complete mitochondrial genome (mtDNA) of snow leopard Panthera uncia was obtained by using the polymerase chain reaction (PCR) technique based on the PCR fragments of 30 primers we designed. The entire mtDNA sequence was 16 773 base pairs (bp) in length, and the base composition was: A-5,357ª“,Ž+bp (31.9%); C-4,444ª”,Ž+bp (26.5%); G-2,428ª“,Ž+bp (14.5%); T-4,544ª”,Ž+bp (27.1%). The structural characteristics [0] of the P. uncia mitochondrial genome were highly similar to these of Felis catus, Acinonyx jubatus, Neofelis nebulosa and other mammals. However, we found several distinctive features of the mitochondrial genome of Panthera unica. First, the termination codon of COIII was TAA, which differed from those of F. catus, A. jubatus and N. nebulosa. Second, tRNASer (AGY), which lacked the ''DHU'' arm, could not be folded into the typical cloverleaf-shaped structure. Third, in the control region, a long repetitive sequence in RS-2 (32ª“,Ž+bp) region was found with 2 repeats while one short repetitive segment (9ª”,Ž+bp) was found with 15 repeats in the RS-3 region. We performed phylogenetic analysis based on a 3 816ª",Ž+bp concatenated sequence of 12S rRNA, 16S rRNA, ND2, ND4, ND5, Cyt b and ATP8 for P. uncia and other related species, the result indicated that P. uncia and P. leo were the sister species, which was different from the previous findings. (c) 2008 Springer Science+Business Media B.V.
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Xu, F., Ming, M., Yin, S. -jing, & Munkhtsog, B. (2006). Autumn Habitat Selection by Snow Leopard (Uncia uncia) in Beita Mountain, Xinjiang, China.
Abstract: Habitat selection of Snow Leopard ( Unica unica) in Beita Mountain of the Altay Mountain system in northeast Xinjiang was conducted from September to October 2004. Six habitat features of 59 sites used by Snow Leopard and 30 random plots were measured by locating 15 transects surveys in the study area . Vanderploge and Scaviaps selectivity index was used to assess Snow Leopardps selection for the different habitat parameters. Principal Component Analysis was used as the primary factor . The results indicated that Snow Leopard preferred the altitude between 2000 – 2 200 m and avoided 2 600 – 3 000 m ; selected cliff base , ridgeline and avoided hillside and valley bottom ; utilized the shrub and rejected the forest ; selected the nongrazing area and avoided the slightly broken region ; preferred north orientation and rejected the south orientation. The results show that grazing status , vegetation type , topography and the ruggedness are the primary factors for the habitat selection of Snow Leopard.
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Ale, S. B., Boesi, R. (2005). Snow Leopard Sightings on the Top of the World. Cat News, (43), 19–20.
Abstract: Sightings of snow leopards Uncia uncia in the wild are rare. This is because snow leopards occur in low numbers and are very elusive (Schaller 1977). Snow leopards may be sparsely distributed,but they may not, however, be very elusive in the world's highest park, Sagarmatha (Mt. Everest) National Park (86° 30' 53“ E to 86° 99' 08” E and 27° 46' 19“ N to 27° 06' 45” N) in Nepal.
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Jackson, R., Hunter, D.O. (1995). Snow leopard Survey and conservation handbook (First edition).
Abstract: The objectives of this handbook (First edition) are to provide standard procedures for conducting snow leopard status and distribution surveys; suggest uniform methods for assessing the status and relative abundance of large prey species (ungulates such as blue sheep, argali, markhor, Himalayan tahr, urial, ibex, red deer, and roe deer); offer guidance in evaluating habitat quality and identifying the major environmental factors affecting species welfare; and provide standard forms for reporting the results of these field surveys, and a process for feeding information developed by the International Snow Leopard Trust into Snoe Leopard Information Management System (SLIMS).
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Johnsingh, A. J. T. (2006). A roadmap for conservation in Uttaranchal.
Abstract: The enchanting state of Uttaranchal, carved out of Uttar Pradesh on 9th November 2000, has a total area of ca. 53,485 km2 with a population density of 160 persons/ km2, much lower than the national average of 324/km2. This young state can take pride in the fact that 13.42% of its area is under protected areas. The state has varied landscapes: snow-capped and conifer forest covered mountains in the north, forest covered foothills with numerous perennial rivers and streams, locally known as the bhabar tract which includes the Himalayan foothills and the Shivalik range. As a result, the land is home to a variety of fascinating wildlife such as the golden mahseer (Tor putitora), king cobra (Ophiophagus hanna), Himalayan monal (Lophophorus impejanus), great hornbill (Buceros bicornis), Himalayan tahr (Hemitragus jemlahicus), bharal (Pseudois nayaur), Himalayan musk deer (Moschus chrysogaster), goral (Nemorhaedus goral), elephant (Elephas maximus), snow leopard (Panthera uncia), leopard (P. pardus), black bear (Ursus thibetanus), and tiger (P. tigris). All across their range, most of these species are endangered. The potential of this state, with about 800 kilometers of riverine habitat, can only be surpassed by Arunachal Pradesh in terms of golden mahseer conservation. The mountains, bedecked with the scarlet flowers of rhododendron (Rhododendron arboreum) in the summer months, can be a veritable home to many forms of pheasants, mountain ungulates and carnivores, provided poaching for trade is eliminated and hunting for the pot is brought under control. The bhabar forests of this state, ca. 7,500 km2, extending between Yamuna and Sharda rivers (Fig. 1.), can easily support a population of about 1000 elephants and 200 tigers as long as this large habitat, now fragmented in three blocks, is managed and protected as one continuous habitat for wildlife. Six villages, gujjar settlements and encroachments need to be moved away from the main wildlife habitat which goes along the bhabar tract. Although the conservation of these habitats can eventually bring in immense benefits through well-planned ecotourism programmes that are rapidly catching up in the state, initial conservation efforts would need a substantial amount of funds.
Keywords: carnivores, conservation, forest, habitat, hunting, landscape, Panthera uncia, poaching, snow leopard, species, tiger, Uncia uncia, ungulates, Uttar Pradesh, Uttaranchal
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