|
|
Suryawanshi, K., K. (2011). Sunshine and the Shadow. Hornbill, (April-June), 34–37.
Abstract: Kulbhushansingh Suryawanshi shares an update on his blog which describes snow leopard sightings in Spiti, Himachal Pradesh, while studying the foraging behavior and eating habits of blue sheep (Pseudois nayaur).
|
|
|
|
Blomqvist, L. (2008). International Pedigree Book for Snow Leopards, Uncia uncia. Helsinki: Helsinki Zoo.
|
|
|
|
Darehshuri, B. F. (1978). Threatened cats of Asia. Wildlife, 20(9), 396–400.
Abstract: Man's hand is turned against the wild cats wherever they occur, often due to the value of their fur, but also because of the danger they sometimes pose to domestic stock and even human beings. All the larger Asian cats are threatened, and on this and the following pages we look at three of them – the Asiatic cheetah, the Siberian tiger, and the snow leopard.
|
|
|
|
Chalise, M. K. (2011). Snow Leopard (Uncia uncia), Prey Species and Outreach in Langtang National, Park, Nepal. Our Nature, (9), 138–145.
Abstract: Presence of snow leopard (Uncia uncia) in Langtang National Park was obscure till 2003. It was confirmed by a
research team trained for the wildlife biology in the field. Along with the study of ecology and behavior of snow leopard sufficient effort were made to generate data on pre species. The study also dealt with threat perceived for the leopard survival while basic unit of conservation- local outreach programs were also initiated.
|
|
|
|
Feng, X., Peng, Q., Chen, Y., Li, W. (2022). A Case Study of the Snow Leopard in Sanjiangyuan National Park Boundaries regarding Park Boundary Divergence. Land, 11(813), 1–15.
Abstract: This paper uses remote sensing data from the Sanjiangyuan National Park (SNP) to explore the divergence between the boundaries of national parks and the distribution of natural habitats. Results are used to argue that these discrepancies evolve along with the potential impact of global warming. Using the example of the habitat change of snow leopards and the conflicts between local people and snow leopards, we reflect on the consequences of this divergence. Results show that divergence between the political boundaries and natural habitats as well as the consequent influence on the living conditions of local people are strikingly visible, and the effects of global warming on such conflicts are apparent. The authors conclude that both notions of ‘political boundaries’ and ‘natural habitats’ are expected to come together as the SNP region is spatially configured, while ‘global warming’ seems to be relevant as an essential reference when delimiting the region in the future. Finally, the proposal for the establishment of cooperative conservation areas is presented,
emphasizing the role of cooperative governance in/around national parks.
|
|
|
|
Mazoomdaar, J. (2011). Cat Among the People. Open, (8 August), 40–45.
|
|
|
|
McCarthy, K., Fuller, T., Ming, M., McCarthy, T., Waits, L., & Jumabaev, K. (2008). Assessing Estimators of Snow Leopard Abundance (Vol. 72).
Abstract: The secretive nature of snow leopards (Uncia uncia) makes them difficult to monitor, yet conservation efforts require accurate and precise methods to estimate abundance. We assessed accuracy of Snow Leopard Information Management System (SLIMS) sign surveys by comparing them with 4 methods for estimating snow leopard abundance: predator:prey biomass ratios, capture-recapture density estimation, photo-capture rate, and individual identification through genetic analysis. We recorded snow leopard sign during standardized surveys in the SaryChat Zapovednik, the Jangart hunting reserve, and the Tomur Strictly Protected Area, in the Tien Shan Mountains of Kyrgyzstan and China. During June-December 2005, adjusted sign averaged 46.3 (SaryChat), 94.6 (Jangart), and 150.8 (Tomur) occurrences/km. We used
counts of ibex (Capra ibex) and argali (Ovis ammon) to estimate available prey biomass and subsequent potential snow leopard densities of 8.7 (SaryChat), 1.0 (Jangart), and 1.1 (Tomur) snow leopards/100 km2. Photo capture-recapture density estimates were 0.15 (n = 1 identified individual/1 photo), 0.87 (n = 4/13), and 0.74 (n = 5/6) individuals/100 km2 in SaryChat, Jangart, and Tomur, respectively. Photo-capture rates
(photos/100 trap-nights) were 0.09 (SaryChat), 0.93 (Jangart), and 2.37 (Tomur). Genetic analysis of snow leopard fecal samples provided minimum population sizes of 3 (SaryChat), 5 (Jangart), and 9 (Tomur) snow leopards. These results suggest SLIMS sign surveys may be affected by observer bias and environmental variance. However, when such bias and variation are accounted for, sign surveys indicate relative abundances similar to photo rates and genetic individual identification results. Density or abundance estimates based on capture-recapture or ungulate biomass did not agree with other indices of abundance. Confidence in estimated densities, or even detection of significant changes in abundance of snow leopard, will require more effort and better documentation.
|
|
|
|
Blomqvist, L. (1979). The 1978 register for the captive population of snow leopards, Panthera uncia. International Zoo News, 26(7-8), 17–23.
|
|
|
|
Mayo, J. G. (1967). Report on the tranquillisation of a male Snow leopard Panthera uncia for semen extraction. International Zoo Yearbook, VII(7), 148–150.
|
|
|
|
Johansson, O., Ullman, K., Lkhagvajav, P., Wiseman, M.,
Malmsten, J., Leijon, M. (2020). Detection and Genetic Characterization of Viruses Present in
Free-Ranging Snow Leopards Using Next-Generation Sequencing. Frontiers in Veterinary Science, 7(645), 1–9.
Abstract: Snow leopards inhabit the cold, arid environments of the high
mountains of South and Central Asia. These living conditions likely
affect the abundance and composition of microbes with the capacity to
infect these animals. It is important to investigate the microbes that
snow leopards are exposed to detect infectious disease threats and
define a baseline for future changes that may impact the health of this
endangered felid. In this work, next-generation sequencing is used to
investigate the fecal (and in a few cases serum) virome of seven snow
leopards from the Tost Mountains of Mongolia. The viral species to which
the greatest number of sequences reads showed high similarity was
rotavirus. Excluding one animal with overall very few sequence reads,
four of six animals (67%) displayed evidence of rotavirus infection. A
serum sample of a male and a rectal swab of a female snow leopard
produced sequence reads identical or closely similar to felid
herpesvirus 1, providing the first evidence that this virus infects snow
leopards. In addition, the rectal swab from the same female also
displayed sequence reads most similar to feline papillomavirus 2, which
is the first evidence for this virus infecting snow leopards. The rectal
swabs from all animals also showed evidence for the presence of small
circular DNA viruses, predominantly Circular Rep-Encoding
Single-Stranded (CRESS) DNA viruses and in one case feline anellovirus.
Several of the viruses implicated in the present study could affect the
health of snow leopards. In animals which are under environmental
stress, for example, young dispersing individuals and lactating females,
health issues may be exacerbated by latent virus infections.
|
|
