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Fox, J. L., Sinha, S.P., Chundawat, R.S. (1992). Activity patterns and habitat use of ibex in the Himalaya mountains of India. Journal of Mammology, 73(3), 527–534.
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Jackson, R. (1984). Radio-tracking snow leopards in the Himalaya: a progress report.
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Anwar, M., Jackson, R., Nadeem, M., Janecka, J., Hussain, S., Beg, M., Muhammad, G., and Qayyum, M. (2011). Food habits of the snow leopard Panthera uncia (Schreber, 1775) in Baltistan, Northern Pakistan. European Journal of Wildlife Research, (3 March), 1–7.
Abstract: The snow leopard (Panthera uncia) inhabits the high, remote mountains of Pakistan from where very little information is available on prey use of this species. Our study describes the food habits of the snow leopard in the Himalayas and Karakoram mountain ranges in Baltistan, Pakistan. Ninety-five putrid snow leopard scats were collected from four sites in Baltistan. Of these, 49 scats were genetically confirmed to have originated from snow leopards. The consumed prey was identified on the basis of morphological characteristics of hairs recovered from the scats. It was found that most of the biomass consumed (70%) was due to domestic livestock viz. sheep (23%), goat (16%), cattle (10%), yak (7%), and cattle–yak hybrids (14%). Only 30% of the biomass was due to wild species, namely Siberian ibex (21%), markhor (7%), and birds (2%). Heavy predation on domestic livestock appeared to be the likely cause of conflict with the local inhabitants. Conservation initiatives should focus on mitigating this conflict by minimizing livestock losses.
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Namgail, T. (2007). Vigilance behaviour of the Tibetan argali Ovis ammon hodgsoni in the Indian Trans-Himalaya. Acta Zoologica Sinica, 53, 195–200.
Abstract: An inverse relationship between individual vigilance level and group size is widely reported in many behavioral studies on animals across several taxa. It is generally held that such a relationship is due to a reduced probability of an individual being killed in larger groups. in the present investigation, I studied the vigilance behavior of the endangered Tibetan argali Ovis ammon hodgsoni in relation to group size and escape terrain. I hypothesized that an individual argali has a higher vigilance level in smaller groups and in habitats closer to cliffs than individuals living in larger groups and open areas (escape terrain). The results show that the vigilance of argali decreased with increasing group size, but there was no effect of escape terrain on its vigilance behavior. There were significant differences between age-sex groups: male, female and yearling in their time budgets. Females, compared to males and yearlings, spent more time being vigilant. They also foraged more and moved less than males. It is suggested that vigilance is an important anti-predator behavior amongst argali sheep.
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Forrest, J. L., Wikramanayake, E., Shrestha, R., Areendran, G., Gyeltshen, K., Maheshwari, A., Mazumdar, S., Naidoo, R., Thapa, G. J., Thapa, K. (2012). Conservation and climate change: Assessing the vulnerability of snow leopard habitat to treeline shift in the Himalaya. Biological Conservation, 150, 129–135.
Abstract: Climate change is likely to affect the persistence of large, space-requiring species through habitat shifts,
loss, and fragmentation. Anthropogenic land and resource use changes related to climate change can also
impact the survival of wildlife. Thus, climate change has to be integrated into biodiversity conservation
plans. We developed a hybrid approach to climate-adaptive conservation landscape planning for snow
leopards in the Himalayan Mountains. We first mapped current snow leopard habitat using a mechanistic
approach that incorporated field-based data, and then combined it with a climate impact model using a
correlative approach. For the latter, we used statistical methods to test hypotheses about climatic drivers
of treeline in the Himalaya and its potential response to climate change under three IPCC greenhouse gas
emissions scenarios. We then assessed how change in treeline might affect the distribution of snow leopard
habitat. Results indicate that about 30% of snow leopard habitat in the Himalaya may be lost due to a
shifting treeline and consequent shrinking of the alpine zone, mostly along the southern edge of the range
and in river valleys. But, a considerable amount of snow leopard habitat and linkages are likely to remain
resilient to climate change, and these should be secured. This is because, as the area of snow leopard habitat
fragments and shrinks, threats such as livestock grazing, retaliatory killing, and medicinal plant collection
can intensify. We propose this approach for landscape conservation planning for other species
with extensive spatial requirements that can also be umbrella species for overall biodiversity.
2012 Elsevier Ltd. All rights reserved
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Suryawanshi, K. R., Bhatnagar, Y. V. B., Redpath, S., Mishra, C. (2013). People, predators and perceptions: patterns of livestock depredation by snow leopards and wolves. Journal of Applied Ecology, 50, 550–560.
Abstract: 1. Livestock depredation by large carnivores is an important conservation and economic concern
and conservation management would benefit from a better understanding of spatial variation
and underlying causes of depredation events. Focusing on the endangered snow leopard
Panthera uncia and the wolf Canis lupus, we identify the ecological factors that predispose
areas within a landscape to livestock depredation. We also examine the potential mismatch
between reality and human perceptions of livestock depredation by these carnivores whose
survival is threatened due to persecution by pastoralists.
2. We assessed the distribution of the snow leopard, wolf and wild ungulate prey through field
surveys in the 4000 km2 Upper Spiti Landscape of trans-Himalayan India. We interviewed local
people in all 25 villages to assess the distribution of livestock and peoples’ perceptions of the risk
to livestock from these carnivores. We monitored village-level livestock mortality over a 2-year
period to assess the actual level of livestock depredation. We quantified several possibly influential
independent variables that together captured variation in topography, carnivore abundance
and abundance and other attributes of livestock. We identified the key variables influencing livestock
depredation using multiple logistic regressions and hierarchical partitioning.
3. Our results revealed notable differences in livestock selectivity and ecological correlates of
livestock depredation – both perceived and actual – by snow leopards and wolves. Stocking
density of large-bodied free-ranging livestock (yaks and horses) best explained people’s threat
perception of livestock depredation by snow leopards, while actual livestock depredation was
explained by the relative abundance of snow leopards and wild prey. In the case of wolves,
peoples’ perception was best explained by abundance of wolves, while actual depredation by
wolves was explained by habitat structure.
4. Synthesis and applications. Our results show that (i) human perceptions can be at odds
with actual patterns of livestock depredation, (ii) increases in wild prey populations will intensify
livestock depredation by snow leopards, and prey recovery programmes must be accompanied
by measures to protect livestock, (iii) compensation or insurance programmes should
target large-bodied livestock in snow leopard habitats and (iv) sustained awareness
programmes are much needed, especially for the wolf.
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Maheshwari, A., Sharma, D., Sathyakumar, S. (2013). Snow Leopard (Panthera Uncia) surveys in the Western Himalayas, India. Journal of Ecology and Natural Environmnet, 5(10), 303–309.
Abstract: We conducted surveys above 3000 m elevation in eight protected areas of Uttarakhand and Himachal Pradesh. These surveys provide new information on snow leopard in Uttarakhand on the basis of indirect evidence such as pugmark and scat. Snow leopard evidence (n = 13) were found between 3190 and 4115 m elevation. On an average, scats (n = 09) of snow leopard were found for every 56 km walked and pugmarks (n = 04) for every 126 km walked. Altogether, about 39% of the evidence were found on the hill-slope followed by valley floor (30%), cliff (15%) and 8% from both stream bed and scree slope. Genetic analysis of the scats identified three different individuals by using snow leopard specific primers. Snow leopard-human conflicts were assessed through questionnaire based interviews of shepherds from Govind Pashu Vihar Wildlife Sanctuary, Askot Wildlife Sanctuary and Nanda Devi Biosphere Reserve areas of Uttarakhand. Surveys revealed that livestock depredation (mule, goat and sheep) is the only cause of snow leopard-human conflicts and contributed 36% of the diet of snow leopard. Blue sheep and rodents together comprised 36.4% of the total diet. We found that 68.1% of the surveyed area was used for pastoral activities in Uttarakhand and Himachal Pradesh and 12.3% area was under tourism, defence and developmental activities.
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Ale, S., Shrestha, B., and Jackson, R. (2014). On the status of Snow Leopard Panthera Uncia (Schreber 1775) in Annapurna, Nepal. Journal of Threatened Taxa, (6(3)), 5534–5543.
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Ferretti, F., Lovari, S., Minder, I., Pellizzi, B. (2014). Recovery of the snow leopard in Sagarmatha (Mt.Everest) National Park: effects on main prey. European Journal of Wildlife Research, (60), 559–562.
Abstract: Consequences of predation may be particularly
heavy on small populations of herbivores, especially if they
are threatened with extinction. Over the 2006–2010 period, we
documented the effects of the spontaneous return of the endangered
snow leopard on the population of the vulnerable
Himalayan tahr. The study area was an area of central
Himalaya where this cat disappeared c. 40 years before, because
of persecution by man. Snow leopards occurred mainly
in areas close to the core area of tahr distribution. Tahr was the
staple (56.3 %) of snow leopards. After the arrival of this cat,
tahr decreased by more than 2/3 from 2003 to 2010 (mainly
through predation on kids). Subsequently, the density of snow
leopards decreased by 60%from2007 to 2010. The main prey
of snow leopards in Asia (bharal, marmots) were absent in our
study area, forcing snow leopards to specialize on tahr. The
restoration of a complete prey spectrum should be favoured
through reintroductions, to conserve large carnivores and to
reduce exploitation of small populations of herbivores, especially
if threatened.
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Kohli, K., Sankaran, M., Suryawanshi, K. R., Mishra, C. (2014). A penny saved is a penny earned: lean season foraging strategy of an alpine ungulate. Animal Behaviour, (92), 93–100.
Abstract: Lean season foraging strategies are critical for the survival of species inhabiting highly seasonal environments
such as alpine regions. However, inferring foraging strategies is often difficult because of
challenges associated with empirically estimating energetic costs and gains of foraging in the field. We
generated qualitative predictions for the relationship between daily winter foraging time, body size and
forage availability for three contrasting foraging strategies including time minimization, energy intake
maximization and net energy maximization. Our model predicts that for animals employing a time
minimization strategy, daily winter foraging time should not change with body size and should increase
with a reduction in forage availability. For energy intake maximization, foraging time should not vary
with either body size or forage availability. In contrast, for a net energy maximization strategy, foraging
time should decrease with increase in body size and with a reduction in forage availability. We contrasted
proportion of daily time spent foraging by bharal, Pseudois nayaur, a dimorphic grazer, across
different body size classes in two high-altitude sites differing in forage availability. Our results indicate
that bharal behave as net energy maximizers during winter. As predicted by the net energy maximization
strategy, daily winter foraging time of bharal declined with increasing body size, and was lower in the
site with low forage availability. Furthermore, as predicted by our model, foraging time declined as the
winter season progressed. We did not find support for the time minimizing or energy intake maximizing
strategies. Our qualitative model uses relative rather than absolute costs and gains of foraging which are
often difficult to estimate in the field. It thus offers a simple way to make informed inferences regarding
animal foraging strategies by contrasting estimates of daily foraging time across gradients of body size
and forage availability.
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