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Jackson, R. (1979). Aboriginal hunting in West Nepal with reference to musk deer (Moschus moschiferous) and the snow leopard (Panthera uncia). Biol.Conservation, 16, 63–72.
Abstract: Describes local hunting methods,economics of hunting and estimated impact on snow leopard populations. Comments on conservation measures taken by government of Nepal
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Jackson, R. (1986). On the trail of the elusive snow leopard. World Wildlife Fund Monthly Report, May, 127–132.
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Jackson, R., & Ahlborn, G. (1986). Himalayan snow leopard project: final progress report, phase 1.
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Jackson, R., & Hillard, D. (1986). Tracking the elusive snow leopard. National Geographic, 169, 792.
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Jackson, R., & Ahlborn, G. (1987). A high altitude survey of the Hongu valley with special emphasis on snow leopard.
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Jackson, R. (1987). Snow Cats of Nepal's Langue Gorge. Animal Kingdom, 4, 44–53.
Abstract: Anecdotal account with some general research results of a four year tracking study of the snow leopard in Nepal's Langu valley
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Jackson, R., & Ahlborn, G. (1989). Catching a ghost (the snow leopard). International Wildlife., 19(3), 30.
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Jackson, R., & Ahlborn, G. (1989). Snow Leopards in Nepal-home range and movements. National Geographic Res., 5, 161–175.
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Jackson, R. (1991). A wildlife survey of the Qomolangma Nature Preserve, Tibetian Autonomous Region, Peoples Republic of China. Franklin, West Virginia: Woodlands Mountain Institute.
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Jackson, R. (1992). Species Survival Commission Plan for Snow Leopard.
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Jackson, R. (1992). SSC Plan for Snow Leopard.
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Jackson, R., & Hunter, D. O. (1995). Snow Leopard Survey and Conservation Handbook (2nd Edition). ISLT and National Biological Survey.
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Jackson, R. M. (1979). Snow Leopards in Nepal. Oryx, 15, 191–195.
Abstract: Reviews in detail occurence, status, and conservation measures related to snow leopards in Nepal. Estimates 150-300 snow leopards in Nepal. Local hunters can get 10 to 50 US dollars for a pelt
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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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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. (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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Jie, Z., & Zongwei, W. (1963). Qinghai Fauna. Journal of Animal, 15(1), 125–137.
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Johnson, D. (1994). The National Fish and Wildlife Foundation goes international. Endangered Species Update, A, 11(10), A10.
Abstract: Abstract: The National Fish and Wildlife Foundation (NFWF) which is a conservation organization created in 1984 aims to conserve the species on an international context before they are endangered which will enable a more effective conservation procedure. The NFWF has addressed the causes of endangered species in India and South Asia such as the tiger, Indian wolf and the snow leopard and has supported the conservation efforts of the Siberian tiger. It has cooperated with multi-national organizations to evaluate the best strategy that could be adopted to prevent a future extinction of several species and has supported CITES programs
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Johnson, W. E., Dratch, P. A., Martenson, J. S., & O'Brien, S. J. (1996). Resolution of recent radiations within three evolutionary lineages of Felidae using mitochondrial restriction fragment length polymorphism variation. Journal of Mammalian Evolution, 3(2), 97–120.
Abstract: Patterns of mitochondrial restriction fragment length polymorphism (RFLP) variation were used to resolve more recent relationships among the species of the Felidae ocelot lineage, domestic cat lineage, and pantherine lineage. Twenty-five of 28 restriction enzymes revealed site variation in at least 1 of 21 cat species. The ocelot lineage was resolved into three separate sister taxa groups: Geoffroy's cat (Oncifelis geoffroyi) and kodkod (O. guigna), ocelot (Leopardus pardalis) and margay (L. wiedii), and pampas cat (Lynchailurus colocolo) and most of the tigrina samples (Leopardus tigrina). Within the domestic cat lineage, domestic cat (Felis catus), European wild cat (F. silvestris), and African wild cat (F. libyca) formed a monophyletic trichotomy, which was joined with sand cat (F. margarita) to a common ancestor. Jungle cat (F. chaus) and black-footed cat (F. nigripes) mtDNAs diverged earlier than those of the other domestic cat lineage species and are less closely related. Within the pantherine lineage, phylogenetic analysis identified two distinct groups, uniting lion (P. leo) with leopard (P. pardus) and tiger (P. tigris) with snow leopard (P. uncia).
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Johnston, L. A., Donoghue, A. M., O'Brien, S. J., & Wildt, D. E. (1991). Rescue and maturation in vitro of follicular oocytes collected from nondomestic felid species. Biol Reprod, 45(6), 898–906.
Abstract: The potential for rescuing immature oocytes from the ovaries of females of rare felid species which die or undergo medical ovariohysterectomy was evaluated. Ovaries were recovered from 13 species representing 35 individuals in good-to-poor health. Although the majority of females were 10 yr of age or older and in fair-to-poor health, a total of 846 oocytes were recovered of which 608 (71.9%) were classified as fair-to- excellent quality. One hundred of these oocytes were used for initial maturation classification and as parthogenetic controls. Overall, of the 508 fair-to-excellent quality oocytes placed in culture, 164 (32.3%) matured to metaphase II in vitro. For species in which 3 or more individuals yielded oocytes, mean oocyte maturation rates were as follows: 36.2%, tiger; 27.9% leopard; and 8.3%, cheetah. In vitro insemination of oocytes resulted in fertilization (2 polar bodies, 2 pronuclei, or cleavage) rates of 9.1% to 28.6% (leopard) using homologous fresh spermatozoa and 4.0% (lion) to 40.0% (puma) using homologous frozen-thawed spermatozoa. Inseminations using heterologous (domestic cat) spermatozoa also resulted in fertilized oocytes in the tiger, leopard, snow leopard, puma, serval, and Geoffroy's cat (range in fertilization rate, 5.0% for leopard to 46.2% for puma). Cleaved embryos resulted from the insemination of leopard oocytes with homologous sperm (n = 1 embryo) and puma oocytes with domestic cat sperm (n = 3 embryos). These results demonstrate that immature ovarian oocytes from rare felid species can be stimulated to mature in vitro despite an excision-to-culture interval as long as 36 h.(ABSTRACT TRUNCATED AT 250 WORDS)
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Johnston, L. A., Armstrong, D. L., & Brown, J. L. (1994). Seasonal effects on seminal and endocrine traits in the captive snow leopard (Panthera uncia). J Reprod Fertil, 102(1), 229–236.
Abstract: The annual reproductive cycle of the male snow leopard (Panthera uncia) was characterized by evaluating seminal and endocrine traits monthly. Testicular volume was greatest (P < 0.05) during the winter months when the quality of ejaculate was optimal. Ejaculate volume, total sperm concentration ml-1, motile sperm concentration per ejaculate, sperm morphology and sperm motility index were lowest during the summer and autumn months compared with the winter and spring. Peripheral LH, FSH and testosterone concentrations were also lowest during the summer months, increasing during the autumn just before the increase in semen quality, and were maximal during the winter months. There was a direct relationship (P < 0.01) between: (1) testosterone and testicular volume, total sperm concentration ml-1, motile sperm concentration per ejaculate and ejaculate volume, and (2) LH and testicular volume and motile sperm concentration per ejaculate. In summary, although spermatozoa were recovered throughout the year, optimal gamete quality was observed during the winter and spring. Although previous studies in felids have demonstrated seasonal effects on either seminal or endocrine traits, this is the first study to demonstrate a distinct effect of season on both pituitary and testicular function.
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Kamelin, R. V. (1990). Gissar Nature Reserve. The reserves in Middle Asia and Kazakstan. Moscow.
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Karesh, W. B., & Kunz, L. L. (1986). Bilateral testicular seminoma in a snow leopard. J Am Vet Med Assoc, 189(9), 1201.
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