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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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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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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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Usgs, & International Snow Leopard Trust. (1995). Snow Leopard Habitat Map. Pakistan: ISLT and World Wide Fund for Nature - Pakistan.
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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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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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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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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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Sulser, C. E., Steck, B. L., & Baur, B. (2008). Effects of construction noise on behaviour of and exhibit use by Snow leopards Uncia uncia at Basel zoo (Vol. 42).
Abstract: Noise caused by human activities can cause stress in animals. We examined whether noise from construction sites affects the behaviour of and exhibit use by three Snow leopards Uncia uncia at Basel zoo. The behaviour and location of the animals were recorded at 1 minute intervals, using the instantaneous scan sampling method over a period of 216 hours (104 hours on noisy days and 112 hours on quiet days). The animals differed individually in their responses to the construction noise. On noisy days, the Snow leopards generally spent less time in locomotion and more time resting, but even on quiet days, resting was the predominant behaviour performed. Under noisy conditions, they increased social resting and decreased resting alone. Walking and social walking were also reduced on noisy days. Furthermore, the Snow leopards spent considerably more time in the remote offexhibit enclosure under noisy conditions. Independent of background noise, they stayed more than half of the time in the caves and the forecourts of the outdoor enclosure. On quiet days, the Snow leopards used more sectors of their exhibit than on noisy days. The results indicate that the Snow leopards responded to construction noise by increasing the amount of time spent resting and by withdrawing to the remote parts of their exhibit.
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