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Jackson, R. M. (1992). Snow Leopard: Imperiled Phantom of Pakistan's High Mountains. Natura, 14(1), 4–9.
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Jackson, R. M. (1996). Home Range, Movements and Habitat use of Snow Leopard (Uncia uncia) in Nepal. Ph.D. thesis, University of London, University of London.
Abstract: Home ranges for five radio-tagged snow leopards (Uncia uncia) inhabiting prime habitat in Nepal Himalaya varied in size from 11-37 km2. These solitary felids were crepuscular in activity, and although highly mobile, nearly 90% of all consecutive day movements involved a straight line distance of 2km or less. No seasonal difference in daily movement or home range boundry was detected. While home ranges overlapped substancially, use of common core spaces was temporally seperated, with tagged animals being located 1.9 km or more apart during the smae day. Spatial analysis indicated that 47-55% of use occured within only 6-15% of total home area. The snow leopards shared a common core use area, which was located at a major stream confuence in an area where topography, habitat and prey abundance appeared to be more favorable. A young female used her core area least, a female with two cubs to the greatest extent. the core area was marked significantly more with scrapes, Faeces and other sighn than non-core sites, suggesting that social marking plays an important role in spacing individuals. Snow leopards showed a strong preference for bedding in steep, rocky or broken terrain, on or close to a natural vegetation or landform edge. linear landform features, such as a cliff or major ridgeline, were preferred for travelling and day time resting. This behavior would tend to place a snow leopard close to its preferred prey, blue sheep (Psuedois nayaur), which uses the same habitat at night. Marking was concetrated along commonly travelled routes, particularly river bluffs, cliff ledges and well defined ridgelines bordering stream confluences--features that were most abundant within the core area. Such marking may facilitate mutual avoidance, help maintain the species' solitary social structure, and also enable a relatively high density of snow leopard, especially within high-quality habitat.
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Jain, N., Wangchuk, R., & Jackson, R. (2003). An Assessment of CBT and Homestay Sites in Spiti District, Himachal Pradesh.
Abstract: The survey described in this report builds upon prior CBT activities undertaken by The Mountain Institute (TMI) in partnership with the Snow Leopard Conservancy (SLC) in Ladakh, supported by a grant from UNESCO (with co-financing from SLC). Under the evolving concept of “Himalayan Homestays”, initially developed and tested in Ladakh, it is proposed that activities be expanded to selected states in India in a strategic and effective way. Himalayan Homestays are part of a larger integrated program to link snow leopard conservation with local livelihoods in Asia.
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Jalanka, H. H. (1989). Medetomidine-induced and ketamine-induced immobilization of snow leopards (Panthera uncia) doses, evaluation and reversal by atipamezole. Journal of Zoo and Wildlife Medicine, 20(2), 154–162.
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Jalanka, H. H. (1989). Evaluation and comparison of 2 ketamine-based immobilization techniques in snow leopards (Panthera uncia). Journal of Zoo and Wildlife Medicine, 20(2), 163–169.
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Jalanka, H. H., & Roeken, B. (1990). The use of Medetomidine, Medetomidine-Ketamine combinations, and Atipamezole in nondomestic mammals: A review. Journal-of-Zoo-and-Wildlife-Medicine, 21(3), 259–282.
Abstract: The recent development of potent and specifica lphar-adrenoceptoar gonistsa nd antagonists has enhanced their use in nondomestic animal immobilization and reversal. Medetomidine, a new potent alphar-agonist, in combination with the dissociative anesthetic ketamine, has been used to immobilize a variety of nondomestic mammals. Medetomidine alone induces sedation in a dose-dependent way, and complete immobilization has been achieved with high doses in semidomesticated reindeer (Rangifer tarandus) and blue foxes (Alopex lagopus). Howbver, we feel that ketamine should be added to the immobilization mixture to ensure complete immobilization and operator safety. In ketamine combinations, medetomidine doses are usually 60-100 pg/kg. The required ketamine doses are remarkably low:0.8-1.6 mglkg in most ruminants,2.5-3.0 mgUgin felids,u rsids,a nd canids,a nd 5.G-8.0m glkgi n primates,w olverines(Gulog ulo),ando therm uitelids. Clinically, the resulting immobilization is characterized by a smooth onset, good to excellent myorelaxation, and areflexia at higher doses. Determinations of hematologic, serum biochemicil, arterial blood gas,a nd acid-bases tatusp arametersi ndicate that the immobilization is physiologically sound. We have had no fatalities attributable to the immobilization mixture ( I ,240 immobilizations). The alphar-adrenoceptora ntagonist,a tipamezole,i s highly efective in reversingt he immobilization induced by medetomidine, medetomidine-ketamine combinations, or xylazine. In ruminants, the medetomidine-ketamine-induced immobilization can be rapidly and persistently reversed by administering 100-l 50 1rg/kg of alipamezole i.v. and the rest s.c., adjusting the total atipamezole dose to an atipamezole: medetomidine ratio of approximately 4-5 (w/w). Becauseth e required ketamine doses are relatively high in carnivores, we prefer to use a lower atipamezole dose (totil atipamezoie: medetomidine ratio approximately 2-3 w/w) and to administer it i.m. or s.c. Using thii regimen, reversals are calm and animals show minimal “residual ketamine effect.” Because atipamezole is a competitive antagonist, its dose should be reduced if it is administered late in the immobilization period when a large part of medetomidine has been endogenously metabolized. Xylazine-induced immobilization is rapidly reversed by I mg of atipamezole for every 8-12 mg of xylazine used.
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Jalanka, H. H. (1991). Medetomidine, medetomidine-ketamine combinations and atipamezole in nondomestic mammals: A clinical, physiological and comparative study. Dep.Clinical Sciences, Coll.Veterinary Med., Helsinki, Finland, .
Abstract: Hibiscus section Furcaria is composed of over 400 species. Kenaf (Hibiscus cannabinus) and rosella (Hibiscus sabdariffa) belong to this section. Both species are important fiber crops. The survey reported in this book was undertaken in order to find new sources of genetic diversity collect, save, and distribute germ plasm. The work contains a taxonomic key of section Furcaria in southern Africa, 8 species, a description of the species illustrated by line-drawings, and distribution maps. (Also discussed are; H. mechowii, H. meeusei, H. surattensis, H. acetosella, H. torrei, H. mastersianus, H. hiernianus, H. altissimus, H. diversifolius sub sp. rivularis.)
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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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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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Jegal, A., Kashkarov, E., & Matyushkin E.N. (2010). Simple method to distinguish tracks of snow leopard and lynx.
Abstract: In the Mongolian and Gobi Altai mountain ranges and also in some other mountains in this region, the
distribution of the snow leopard and Eurasian lynx overlaps. In some cases, local hunters cannot
distinguish the tracks of both these animals. Therefore we outline a simple method to distinguish tracks of
the snow leopard and lynx.
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