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Lui, C. -guang, Zheng, C. -wu, & Ren, J. -rang. (2003). Research Foods and Food Sources About Snow Leopard (Panthera uncia) (Vol. 31).
Abstract: During 1984-1987, 1992-1995, and 1998-2001, the author researched snow leopard, white lipped deer, kiang, and argali in Qinghai, Gansu, Xingiang, and Sichuan. He collected 644 snow leopard droppings, and analyzed kinds of foods and sources from perch. Snow leopard's foods include most main foods, main foods, comparative foods and lesser foods. Studied one another
index of faunistic congruence of foods species that from various distribution and variation both perch vertical variety and foods of snow leopard.
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Flora and Fauna International. (2006). Central Asia Snow Leopard Workshop. Author.
Abstract: Meeting report for the Central Asia Snow Leopard Workshop, held in Bishkek in June 2006.
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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.
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Saparbayev, S.K., & Woodward, D. B. (2008). Snow Leopard (Uncia uncia) as an Indicator Species and Increasing Recreation Loads in the Almaty Nature Reserve.
Abstract: The purpose of this research is to analyze the data on ecology, biology and dynamics of snow leopard population in the Almaty Nature Reserve and to identify if the increasing numbers of ecotourists could contribute to the decrease of Uncia uncia population. The results of the study show that increasing recreation loads in the Reserve and adjacent territories elevate the disturbance level to the snow leopard's main prey Siberian Ibex and to the predator itself that could result in a decrease of population of this endangered species or its total extinction.
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Janecka, J.E., Jackson, R., Yuquang, Z., Diqiang, L., Munkhtsog, B., et al. (2008). Population monitoring of snow leopards using noninvasive collection of scat samples: a pilot study (Vol. 11).
Abstract: The endangered snow leopard Panthera uncia occurs in rugged, high-altitude regions of Central Asia. However, information on the status of this felid is limited in many areas. We conducted a pilot study to optimize molecular markers for the analysis of snow leopard scat samples and to examine the feasibility of using noninvasive genetic methods for monitoring this felid. We designed snow leopard-specific primers for seven microsatellite loci that amplified shorter segments and avoided flanking sequences shared with repetitive elements. By redesigning primers we maximized genotyping success and minimized genotyping errors. In addition, we tested a Y chromosome-marker for sex identification and designed a panel of mitochondrial DNA primers for examining genetic diversity of snow leopards using scat samples. We collected scats believed to be from snow leopards in three separate geographic regions including north-western India, central China and southern Mongolia. We observed snow leopard scats in all three sites despite only brief 2-day surveys in each area. There was a high rate of species misidentification in the field with up to 54% of snow leopard scats misidentified as red fox. The high rate of field misidentification suggests sign surveys incorporating scat likely overestimate snow leopard abundance. The highest ratio of snow leopard scats was observed in Ladakh (India) and South Gobi (Mongolia), where four and five snow leopards were detected, respectively. Our findings describe a species-specific molecular panel for analysis of snow leopard scats, and highlight the efficacy of noninvasive genetic surveys for monitoring snow leopards. These methods enable large-scale noninvasive studies that will provide information critical for conservation of snow leopards.
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Ale, S. B., Yonzon, P., & Thapa, K. (2007). Recovery of snow leopard Uncia uncia in Sagarmatha (Mount Everest) National Park, Nepal (Vol. 41).
Abstract: From September to November 2004 we conducted surveys of snow leopard Uncia uncia signs in three major valleys in Sagarmatha (Mount Everest) National Park in Nepal using the Snow Leopard Information Management System, a standardized survey technique for snow leopard research. We walked 24 transects covering c. 14 km and located 33 sites with 56 snow leopard signs, and 17 signs incidentally in other areas. Snow leopards appear to have re-inhabited the Park, following their disappearance c. 40 years ago, apparently following the recovery of Himalayan tahr Hemitragus jemlahicus and musk deer Moschus chrysogaster populations. Taken together the locations of all 73 recent snow leopard signs indicate that the species is using predominantly grazing land and shrubland/ open forest at elevations of 3,000-5,000 m, habitat types that are also used by domestic and wild ungulates. Sagarmatha is the homeland of c. 3,500 Buddhist Sherpas with .3,000 livestock. Along with tourism and associated developments in Sagarmatha, traditional land use practices could be used to ensure coexistence of livestock and wildlife, including the recovering snow leopards, and ensure the wellbeing of the Sherpas.
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Blomqvist, L., & Dexel, B. (2006). In Focus: Declining numbers of wild snow leopards.
Abstract: International collaboration to ensure the long-term survival of snow leopards (Uncia uncia) in the wild is today more acutely needed than ever! Trade in live snow leopards, their skins and bones, has during the last decade reached such extensiveness that the species is in danger of being wiped out from many of its former habitats. All recent surveys support declining populations throughout most of their range.
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Helman, R. G., Russell, W. C., Jenny, A., Miller, J., & Payeur, J. (1998). Diagnosis of tuberculosis in two snow leopards using polymerase chain reaction (Vol. 10).
Abstract: The incidence of tuberculosis in zoological animal collections is low, and the disease is monitored through skin testing primarily in primates and artiodactylids.15,16 Other exotic animals are clearly at risk; tuberculosis has been described in elephants (Mycobacterium tuberculosis, M. bovis), rhinoceros (M. bovis), felids (M. bovis), foxes (M. bovis), birds (M. avium complex, M. tuberculosis, M. bovis), and reptiles, amphibians, and fish (cryophilic Mycobacterium species). 1,2,4,6,8-10,13,14,17 Mycobacterial infections in mammals and birds serve as a potential source of disease that can spread to other animals and to humans.7,15,16 In humans, M. bovis and M. tuberculosis are the most important mycobacteria in the USA.
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Jackson, R., & Wangchuk, R. (2004). A Community-Based Approach to Mitigating Livestock Depredation by Snow Leopards (Vol. 9).
Abstract: Livestock depredation by the endangered snow leopard (Panthera uncia) _is an increasingly contentious issue in Himalayan villages, especially in or near protected areas. Mass attacks in which as many as 100 sheep and goats are killed in a single incident inevitably result in retaliation by local villagers. This article describes a community-based conservation initiative to address this problem in Hemis National Park, India. Human-wildlife conflict is alleviated by predator-proofing villagers' nighttime livestock pens and by enhancing household incomes in environmentally sensitive and culturally compatible ways. The authors have found that the highly participatory strategy described here (Appreciative Participatory Planning and Action-APPA) leads to a sense of project ownership by local stakeholders, communal empowerment, self-reliance, and willingness to co-exist with
snow leopards. The most significant conservation outcome of this process is the protection from retaliatory poaching of up to five snow leopards for every village's livestock pens that are made predator-proof._
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Janovsky, M., Grone, A., Ciardo, D., Vollm, J., Burnens, A., Fatzer, R., et al. (2006). Phaeohyphomycosis in a Snow Leopard (Uncia uncia) due to Cladophialophora bantiana (Vol. 134).
Abstract: Phaeohyphomycosis caused by Cladophialophora bantiana was diagnosed in a 5-month-old snow leopard with spastic paralysis of the hind legs and inability to defaecate or urinate. At post-mortem examination, a greenish soft mass resembling an abscess was found on one side of the epidural space at the fourth lumbar vertebral body. Histological examination revealed a purulent meningitis with myelomalacia. Dematiaceous fungal hyphae, present within the inflammatory infiltrate, were identified as C. bantiana by culture and sequence analysis of the 18S ribosomal RNA gene. This neurotropic fungus rarely affects organs other than the brain in human beings and cats, and has been reported only occasionally in Europe. The case described suggests that phaeohyphomycosis due to C. bantiana infection may be recognized more frequently in the future and the possible involvement of organs other than the brain should be borne in mind.
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