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Subbotin, A. E., & Istomov, S. V. (2009). The population status of snow leopards Uncia uncia (Felidae, Carnivora) in the western Sayan Mountain Ridge. Doklady Biologicl Sciences, 425, 183–186.
Abstract: The snow leopard (Uncia uncial Schreber, 1776) is the most poorly studied species of the cat family in the world and, in particular, in Russia, where the northern periphery of the species area (no more than 3% of it) is located in the Altai-Hangai-Sayan range [1]. It is generally known that the existing data on the Russian part of the snow leopard population have never been a result of targeted studies; at best, they have been based on recording the traces of the snow leopard vital activity [2]. This is explained by the snow leopard's elusive behavior, inaccessibility of its habitats for humans, and its naturally small total numbers in the entire species area. All published data on the population status of the snow leopard in Russia, from the first descriptions of the species [3-6] to the latest studies [7, 8] are subjective, often speculative, and are not confirmed by
quantitative estimates. It is obvious, however, that every accurate observation of this animal is of particular interest [9]. The purpose of our study was to determine the structure and size of the population group presumably inhabiting the Western Sayan mountain ridge at the northern boundary of the species area
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Sunquist, F. (1997). Where cats and herders mix. (snow leopards in Tibet and Mongolia). International Wildlife, 27(1), 27–33.
Abstract: The snow leopard inhabits a huge range of territory which encompasses some of Central Asia's most bleak and inhospitable terrains. The animal herders in these regions are desperately poor and yet they have agreed to cooperate with conservation groups in protecting the snow leopard. The World Wildlife Foundation has worked to create a refuge on the Pakistan-China border. Sheep herders near Askole, a village in the Baltistan region of northern Paksitan, drive their flocks past stone enclosures. The area is also home to snow leopards. With their natural prey dminished, leopards in 13 countries of central Asia occasionally feed on livestock, putting the cats on a collision course with mountain peoples.
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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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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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Thapa, K. (2005). Is their any correlation between abundance of blue sheep population and livestock depredation by snow leopards in the Phu Valley, Manang District, Annapurna Conservation Area? Final report.
Abstract: This study was undertaken in the Phu valley of Manang district in the Annapurna Conservation Area, Nepal,
Spring, 2004 and 2005. I used the Snow Leopard Management Information System (“second order” survey technique), to determine
the relative abundance of snow leopards in delineated areas in Phu valley. Transects routes were plotted by
randomly selected feasible landforms such as along ridgelines, cliff bases and river bluffs where snow
leopards sign is likely to be found. Altogether, 16 transects (total length of 7.912 km) were laid down (mean
transect length=0.495 km). They revealed, 54 sign sites (both relic and non-relic) and altogether 88 signs (72
scrapes, 11 feces, 3 scent mark, 2 pugmarks and 1 hair) were recorded (6.8 site/km and 11.1 signs/km). There
were 61.1% non-relic and 38.9% relic sites. The density of snow leopards in Phu Valley may be 4-5 snow
leopards/100 kmý.It was found that the Ghyo block had the highest sign density (13.6 mean sign item/km)
and Phu block (9.8 mean sign item/km) and the lowest in Ngoru block (3.9 mean sign item/km.). For blue sheep, direct count method was applied from different appropriate vantage points (fixed-point
count). I counted total individuals in each herd and classified all individuals whenever possible, using 8 X24
binocular and 15-60x spotting scope. A total 37 blue sheep herds and 1209 individuals were observed in
192.25 kmý of the study area (blue sheep density, 6.3 kmý). Average herd size was 32.68. Herd size varied
from 1 to 103 animals (the largest so far recorded). The average sex ratio male to female for the entire survey
area was 0.67. Recruitment rate was 47.13. The ratio of yearlings to adult female was 0.45. In Ghyo block
had total 168 blue sheep (area, 44.08 km2 or 3.8/ km2 i.e. 137.2 kg/ kmý). Blue sheep density in Ngoru block
showed 4.7/km2 (area, 65.47 km2). Highest density of blue sheep among three blocks was recorded in Phu
block, 8.9/km2 (or 320 kg/km2) in its 82.70 km2 area. A standard questionnaire was designed, and interviews conducted for relevant information was collected on
livestock depredation patterns (total household survey). Out of 33 households surveyed, 30 reported that they
had livestock depredation by the snow leopard in 2004. Altogether 58 animals were reportedly lost to snow
leopards (3.1% of the total mortality). Out of the estimated standing available biomass (1, 83,483kg) in the
Phu valley at least 2220 kg or 1.3% of the total livestock biomass was consumed by snow leopards in the
year of our study (2004). It was estimated that in the Phu valley annually 1.8 animals were lost per household
to snow leopards. This means approx. Rs.413560 (US$ 5,908) is lost annually in the valley (US$
179/household/annum). Ghyo block, had the highest animals loss (53.4%), followed by Phu block (36.2%)
and Ngoru block (10.3%) to snow leopards. There is positive correlation among the densities of blue sheep, relative abundance of the snow leopard and
livestock depredation. Blue sheep is the main prey species of the snow leopard in Phu valley and its
conservation therefore matters to reduce livestock depredation. A general patterns appears here that shows
that blue sheep (prey) abundance determine snow leopard (predator) abundance and that livestock
depredation by snow leopards may be minimal where there is good population of blue sheep, and vice versa.
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Trivedi, P. (2009). Project Snow Leopard: Participatory conservation model for the Indian Himalaya. Mountain Forum Bulletin, Ix(2), 52–54.
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Usgs, & International Snow Leopard Trust. (1995). Snow Leopard Habitat Map. Pakistan: ISLT and World Wide Fund for Nature - 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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Velte, F. (1982). Snow leopards at the Seneca Zoological Park, Rochester. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 55–58). Helsinki: Helsinki Zoo.
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Vogt, P. (1982). New enclosures for snow leopards (Uncia uncia) at Krefeld Zoo. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 67–70). Helsinki: Helsinki Zoo.
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Wahlberg, C., Tarkkanen, A., & Blomqvist, L. (1982). Further observations on the multiple ocular coloboma (MOC) in the snow leopard, Panthers uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 3, pp. 139–144). Helsinki: Helsinki Zoo.
Abstract: The first observation of the occurrence of multiple ocular coloboma (MOC) in a snow leopard was reported in the International Pedigree Book of Snow Leopards Volume I in 1978 (1). The lesions in this syndrome consist of coloboma of the upper eye lid and uveal coloboma of the globe. Even colobomatous retinal cysts and retinal dysplasia have been noted. The ethiology of in all ten cases of MOC in the snow leopards kept at the Helsinki Zoo were described and discussed in detail in Volume II of the International Pedigree Book of Snow Leopards (2,3). Three cases of MOC in the snow leopards kept at Henry Doorly Zoo, Omaha, Ne., have been described by Phillips (4), one case is known of in Amsterdam (van Bree, personal communication), and two cases in Zoo Zurich (Isenbugel and Weilenmann, pers. comm.) The ethiology of the defect is still not known although various theories ranging from genetic to exogenous factors have been presented.
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Wahlberg, C. (1980). Autopsy findings and causes of death in captive snow leopards (Panthera uncia): a preliminary report. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 205–217). Helsinki: Helsinki Zoo.
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Wahlberg, C., & Tarkkanen, A. (1980). On the multiple ocular coloboma with retinal dysplasia (MOC) in snow leopards, Pantera uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (Vol. 2, pp. 183–194). Helsinki: Helsinki Zoo.
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Wangchuk, R., & Jackson, R. (2009). A Community-based Approach to Mitigating Livestock-Wildlife Conflict in Ladakh, India.
Abstract: Livestock depredation by snow leopard and wolf is widespread across the Himalayan region (Jackson et al. 1996, Jackson and Wangchuk 2001; Mishra 1997, Oli et al 1994). For example, in India's Kibber Wildlife Sanctuary, Mishra (1997) reported losses amounting to 18% of the livestock holdings and valued at about US $138 per household. The villagers claimed predation rates increased after establishment of the sanctuary, but
surveys indicated a dramatic increase in livestock numbers accompanying changes in animal husbandry systems (Mishra 2000).
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Weilenmann, P. (1978). First experiences in keeping snow leopards in the Zurich Zoo. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 1 (Vol. 1, pp. 35–43). Helsinki: Helsinki Zoo.
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Weilemann P. (1982). Experiences in births of snow leopards in Zurich Zoo. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 111–116). Helsinki: Helsinki Zoo.
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Wharton, D., & Mainka, S. A. (1986). Snow leopards, livestock management. China: Xinjiang Conservation Fund & International Snow Leopard Trust.
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Worley, M. B. (1982). Hypogammaglobulinemia in snow leopards. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 129–130). Helsinki: Helsinki Zoo.
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Worley, M. B. (1982). Chronic liver disease in snow leopards: A possible viral etiology. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 131–133). Helsinki: Helsinki Zoo.
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Anonymous. (2000). Snow leopard management plan of Mongolia (draft).
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Xu, F., Ming, M., Yin, S. -jing, & Mardan. (2005). Snow Leopard Survey in Tumor Nature Reserve, Xingjiang (Vol. 24).
Abstract: Snow leopard survey was conducted in Oct-Nov 2004 at Tumor National Natural Reserve, Xinjiang, China. Because of its special living style, the snow leopard is difficult to observe by sight. Signs left by snow leopard become a good index to prove the existance of the big cat. There are mainly five kinds of signs, footprints, fectes, claw rakes and urine spray. From them we can know the distribution, probably population and habitat selection of snow leopard. This time in Tumor we investigated 5 difference places: Pochenzi in Mozat River area, Boxidun in Little Kuzbay River area, Yinyer in Tomur River area, Kurgan and Taglak in Quiong Tailan River area. 42 transects were run in this trip and a total of 57 signs found. Among them, footprints amounted to 71.9%, scrapes 21.1%, and feces 7.0%. The results showed that the big cat existed in Yinyer, Kurgan and Taglak areas and liked to select their habitat in the valley and didn't like to live in barren areas.
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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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Yanfa, L. (1985). A preliminary investigation into the geographic distribution of the snow leopard Panthera uncia Schreber. Acta Theriologica Sinica, 5(3), 184–188.
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Yu, N. Z. C., Wang, X., He, G., Zhang, Z., Zhang, A., Lu, W., et al. (1996). A revision of genus Uncia Gray, 1854 based on mitochondrial DNA restriction site maps. Acta Theriologica Sinica, 16(2), 105–108.
Abstract: The Snow leopard (Panthera uncia) is one of the most threatened wild big cats within its range of distribution, however, the question of its systematic status is a matter of debate. Is it a member of genus Panthera, or is it in its own genus (Uncia)? The analysis of genetic difference at the DNA level may provide useful data to clarify the issue. In the present study, ten hexanucleotide-specific restriction endonucleases were used to evaluate the patterns of mitochondrial DNA variation between the Snow leopard and leopard (P. pardus). The molecular size of mtDNA from the two species was about 16.5 kb. Ten enzymes surveyed 32-34 restriction sites, which corresponded to 192 apprx 204 base pairs, or 1.16% apprx 1.24% of the total mtDNA molecule. A total of 45 restriction sites were mapped; of these sites, twenty-four, which correspond to 53.3% of the total sites, were variable. The sequence divergence between them was 0.075 33, which was undoubtedly in the species-level distinction but did not reach the genus level. Therefore, the Snow leopard should be placed in the genus Panthera rather than in its own ganus. It also seems reasonable to recognize Uncia as a valid subgenus. This conclusion not only support but also supplement the viewpoint of Simpson who treated Uncia as a subgenus within Panthera.
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Zahler, P., & Graham, P. (2001). War and wildlife: the Afghanistan conflict and its effects on the environment. Seattle: International Snow Leopard Trust.
Abstract: The International Snow Leopard Trust (ISLT) is a nonprofit environmental organization dedicated to the conservation of the endangered snow leopard and its mountain ecosystem through a balanced approach that considers the needs of the local people and the environment. As such, we wish to stress that the ISLT does not have a position regarding the present conflict in Afghanistan. However, this organization believes that there are important repercussions regarding this conflict that have yet to be addressed in the media, within government circles, or among the public. This report documents some of these repercussions so that they may be included in the present dialog.
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