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Li, J., McCarthy, T. M., Wang, H., Weckworth, B. V., Shaller, G. B., Mishra, C., Lu, Z., Beissinger, S. R. (2016). Climate refugia of snow leopards in High Asia. Biological Conservation, (203), 188–196.
Abstract: Rapidwarming in High Asia is threatening its unique ecosystemand endemic species, especially the endangered
snow leopard (Panthera uncia). Snow leopards inhabit the alpine zone between snow line and tree line, which
contracts and expands greatly during glacier-interglacial cycles. Here we assess impacts of climate change on
global snow leopard habitat from the last glacial maximum (LGM; 21 kyr ago) to the late 21st century. Based
on occurrence records of snow leopards collected across all snow leopard range countries from 1983 to 2015,
we built a snow leopard habitat model using the maximum entropy algorithm (MaxEnt 3.3.3k). Then we
projected this model into LGM, mid-Holocene and 2070. Analysis of snow leopard habitat map from LGM to
2070 indicates that three large patches of stable habitat have persisted from the LGM to present in the Altai,
Qilian, and Tian Shan-Pamir-Hindu Kush-Karakoram mountain ranges, and are projected to persist through the
late 21st century. These climatically suitable areas account for about 35% of the snow leopard's current extent,
are large enough to support viable populations, and should function as refugia for snow leopards to survive
through both cold and warm periods. Existence of these refugia is largely due to the unique mountain environment
in High Asia, which maintains a relatively constant arid or semi-arid climate. However, habitat loss leading
to fragmentation in the Himalaya and Hengduan Mountains, as well as increasing human activities, will present
conservation challenges for snow leopards and other sympatric species.
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Jackson, R., Roe, J., Wangchuk, R., & Hunter, D. (2005). Camera-Trapping of Snow Leopards. Cat News, 42(Spring), 19–21.
Abstract: Solitary felids like tigers and snow leopards are notoriously difficult to enumerate, and indirect techniques like pugmark surveys often produce ambiguous information that is difficult to interpret because many factors influence marking behavior and frequency (Ahlborn & Jackson 1988). Considering the snow leopard's rugged habitat, it is not surprising then that information on its current status and occupied range is very limited. We adapted the camera-trapping techniques pioneered by Ullas Karanth and his associates for counting Bengal tigers to the census taking of snow leopards in the Rumbak watershed of the India's Hemis High Altitude National Park (HNP), located in Ladakh near Leh (76ø 50' to 77ø 45' East; 33ø 15' to 34ø 20'North).
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Fox, J. L. (1991). Wildlife Ecology Workshop Held in Indias Himalaya Region (Vol. ix). Seattle: Islt.
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Filla, M., Lama, R. P., Filla, T., Heurich, M., Balkenhol, N., Waltert, M., Khorozyan, I. (2022). Patterns of livestock depredation by snow leopards and effects of intervention strategies: lessons from the Nepalese Himalaya. Wildlife Research, .
Abstract: Context: Large carnivores are increasingly threatened by anthropogenic activities, and their protection is among the main goals of biodiversity conservation. The snow leopard (Panthera uncia) inhabits high-mountain landscapes where livestock depredation drives it into conflicts with local people and poses an obstacle for its conservation.
Aims: The aim of this study was to identify the livestock groups most vulnerable to depredation, target them in implementation of practical interventions, and assess the effectiveness of intervention strategies for conflict mitigation. We present a novel attempt to evaluate intervention strategies for particularly vulnerable species, age groups, time, and seasons.
Methods: In 2020, we conducted questionnaire surveys in two regions of the Annapurna Conservation Area, Nepal (Manang, n = 146 respondents and Upper Mustang, n = 183). We applied sample comparison testing, Jacobs’ selectivity index, and generalised linear models (GLMs) to assess rates and spatio-temporal heterogeneity of depredation, reveal vulnerable livestock groups, analyse potential effects of applied intervention strategies, and identify husbandry factors relevant to depredation.
Key results: Snow leopard predation was a major cause of livestock mortality in both regions (25.4–39.8%), resulting in an estimated annual loss of 3.2–3.6% of all livestock. The main intervention strategies (e.g. corrals during night-time and herding during daytime) were applied inconsistently and not associated with decreases in reported livestock losses. In contrast, we found some evidence that dogs, deterrents (light, music playing, flapping tape, and dung burning), and the use of multiple interventions were associated with a reduction in reported night-time depredation of yaks.
Conclusions and implications: We suggest conducting controlled randomised experiments for quantitative assessment of the effectiveness of dogs, deterrents, and the use of multiple interventions, and widely applying the most effective ones in local communities. This would benefit the long-term co-existence of snow leopards and humans in the Annapurna region and beyond.
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Brown, J. L., Wasser, S. K., Wildt, D. E., & Graham, L. H. (1994). Comparative Aspects of Steroid Hormone Metabolism and Ovarian Activity in Felids, Measured Noninvasively in Feces. Biol Reprod, 51(4), 776–786.
Abstract: Noninvasive fecal assays were used to study steroid metabolism and ovarian activity in several felid species. Using the domestic cat (Felis catus) as model, the excretory products of injected [14C]estradiol (E2) and [14C]progesterone (P4) were determined. Within 2 days, 97.0 +/- 0.6% and 96.7 +/- 0.5% of recovered E2 and P4 radioactivity, respectively, was found in feces. E2 was excreted as unconjugated estradiol and estrone (40%) and as a non-enzyme- hydrolyzable conjugate (60%). P4 was excreted primarily as non-enzyme- hydrolyzable, conjugated metabolites (78%) and as unconjugated pregnenolone epimers. A simple method for extracting fecal steroid metabolites optimized extraction efficiencies of the E2 and P4 excretion products (90.1 +/- 0.8% and 87.2 +/- 1.4%, respectively). Analysis of HPLC fractions of extracted fecal samples from the radiolabel-injected domestic cats revealed that E2 immunoreactivity coincided primarily with the unconjugated metabolized [14C]E2 peak, whereas progestogen immunoreactivity coincided with a single conjugated epimer and multiple unconjugated pregnenolone epimers. After HPLC separation, similar immunoreactive E2 and P4 metabolite profiles were observed in the leopard cat (F. bengalensis), cheetah (Acinonyx jubatus), clouded leopard (Neofelis nebulosa), and snow leopard (Panthera uncia). Longitudinal analyses demonstrated that changes in fecal E2 and P4 metabolite concentrations reflected natural or artificially induced ovarian activity. For example, severalfold increases in E2 excretion were associated with overt estrus or exogenous gonadotropin treatment, and elevated fecal P4 metabolite concentrations occurred during pregnant and nonpregnant (pseudopregnant) luteal phases. Although overall concentrations were similar, the duration of elevated fecal P4 metabolites during pseudopregnancy was approximately half that observed during pregnancy. In summary, steroid metabolism mechanisms appear to be conserved among these physically diverse, taxonomically related species. Results indicate that this hormone-monitoring approach will be extremely useful for elucidating the hormonal regulatory mechanism associated with the reproductive cycle, pregnancy, and parturition of intractable and endangered felid species.
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Aryal, A. (2009). Final Report On Demography and Causes of Mortality of Blue Sheep (Pseudois nayaur) in Dhorpatan Hunting Reserve in Nepal.
Abstract: A total of 206 individual Blue sheep Pseudois nayaur were estimated in Barse and Phagune blocks of Dhorpatan Hunting Reserve (DHR) and population density was 1.8 Blue sheep/sq.km. There was not significant change in population density from last 4 decades. An average 7 animals/herd (SD-5.5) were classified from twenty nine herds, sheep per herds varying from 1 to 37. Blue sheep has classified into sex ratio on an average 75 male/100females was recorded in study area. The sex ratio was slightly lower but not significantly different from the previous study. Population of Blue sheep was seen stable or not decrease even there was high poaching pressure, the reason may be reducing the number of predators by poison and poaching which has
supported to increase blue sheep population. Because of reducing the predators Wolf Canis lupus, Wild boar population was increasing drastically in high rate and we can observed wild boar above the tree line of DHR. The frequency of occurrence of different prey species in scats of different predators shows that, excluding zero values, the frequencies of different prey species were no significantly different (ö2= 10.3, df = 49, p > 0.05). Most of the scats samples (74%) of Snow leopard, Wolf, Common Leopard, Red fox's cover one prey species while two and three species were present in 18% and 8%, respectively. Barking deer Muntiacus muntjak was the most frequent (18%) of total diet composition of common leopards. Pika Ochotona roylei was the most frequent (28%), and Blue sheep was in second position for diet of snow leopards which cover 21% of total diet composition. 13% of diet covered non-food item such as soil, stones, and vegetable. Pika was most frequent on Wolf and Red fox diet which covered 32% and 30% respectively. There was good positive relationship between the scat density and Blue sheep consumption rate, increasing the scat density, increasing the Blue sheep consumption rate. Blue sheep preference by different predators such as Snow leopard, Common leopard, Wolf and Red fox were 20%, 6%, 13% and 2% of total prey species respectively.
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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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