33 research outputs found

    High Altitude Wetlands of Nepal

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    Currently there is no precise definition available in the scientific literature for the term high altitude wetlands (HAWs), however Chatterjee et al. (2010) describe HAWs as "areas of swamp, marsh, meadow, fen, peat land, or water located at an altitude above 3,000 m, whether natural or artificial, permanent or temporary, with water that is static or flowing, fresh, brackish, or saline and are generally located at altitude between continuous natural forest border and the permanent snow." HAWs include different categories of water bodies, such as lakes, ponds, rivers, glaciers, and glacial lakes. They are characterized by a unique diversity of water sources, habitats, species, and communities and generally have not been subjected to rampant human interference compared to other wetland ecosystems. Nepal is blessed with the highest peak in the world, Mt. Everest, along with another ten of the fourteen highest peaks, all over 8,000 m. These mountains are the source of many glaciers and lakes in the high altitude regions across the country. Most of the high altitude wetlands in South Asia, including Nepal, lie within the Hindu Kush Himalayan Region that extends over 3,500 km and covers approximately 3.5 million sq. km., acting as a fresh water reservoir to the major river basins such as the Ganges, Indus, Yangtze, Mekong, Amu Darya, and Hilmand (Gujja 2005)

    The effects of feeding and transport length on the welfare of white rhinoceroses (Ceratotherium simum simum) during long-distance translocations: a preliminary study

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    Translocation is a valuable conservation tool, but poses significant risks for the transported rhinoceroses. Interventions reducing these risks are required to ensure positive welfare during transportation. The aim of this study was to evaluate the effect of journey duration and feeding during the transport of white rhinoceroses (Ceratotherium simum simum). A total of 32 animals were transported by road during two events, five days apart. Fifteen rhinoceroses in the first transport event (37.0 ± 2.4 hr duration) were not fed, while 17 rhinoceroses in the second event (32.2 ± 1.5 hr duration) were offered lucerne. Blood samples were collected at capture and after transport for the evaluation of changes in serum clinical chemistry analytes. The Wilcoxon rank-sum test was used to compare differences between the groups. In all rhinoceroses, transport resulted in changes in serum electrolyte, metabolite and enzyme concentrations, indicating a loss in total body water, nutritional shifts, stress and fatigue. Fed rhinoceroses, transported over a shorter time, displayed greater changes in osmolality (p< 0.006), serum sodium and chloride concentrations (p = 0.005 and = 0.001, respectively) indicating a greater degree of total body water loss than non-fed rhinoceroses. Feeding and a shorter transport duration reduced, but did not prevent, nutritional challenges. A greater increase in the muscle enzymes CK and AST (p = 0.027 and = 0.001, respectively), indicated greater fatigue in non-fed rhinoceroses transported over a longer time. Further work to distinguish the effects of feeding and journey duration is required to better understand the role feeding may play in mitigating welfare challenges during rhinoceros translocation
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