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  • 2000-2004  (4)
  • 1
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Habitat degradation and climate change are thought to be altering the distributions and abundances of animals and plants throughout the world, but their combined impacts have not been assessed for any species assemblage. Here we evaluated changes in the distribution sizes and abundances of 46 ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant pathology 49 (2000), S. 0 
    ISSN: 1365-3059
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Common agricultural weeds and crops that grow in the high hills of Nepal were examined after artificial inoculation and under natural conditions in the UK and Nepal to determine whether such plant species could act as hosts to biovar 2 of Ralstonia solanacearum. Bacterial populations in the roots were determined 1 and 2 months after inoculation, and at various intervals after harvesting infected potato crops under natural conditions. Inoculated roots of the summer weeds Drymaria cordata and Polygonum capitata and the winter weeds Cerastium glomeratum and Stellaria media yielded 102−107 colony-forming units per g root. High populations of the bacterium were recovered from these plants even after partial surface sterilization, indicating that systemic infection had occurred. Ralstonia solanacearum populations were recovered from root extracts of 75% of naturally growing D. cordata plants when sampled 3 months after harvest of a potato crop with bacterial wilt. Similarly, root extracts of 25% of P. capitata plants carried the bacterium. No potential winter weed hosts were infected under natural conditions when sampled 5 and 6 months after harvest of infected potato, indicating that winter conditions in the high hills of Nepal are not conducive to infection. Among crops, mustard (Brassica juncea cv. Fine White) developed typical wilt symptoms after artificial inoculation in warm glasshouse conditions (20–28°C). Mustard and barley are winter crops in Nepal. However, neither mustard (Brassica juncea var. Lumle Tori) nor barley (Hordeum vulgare cv. Bonus) was infected when planted into heavily infested plots under natural conditions. The results indicated that the role of nonsolanaceous summer weeds in the persistence of biovar 2 of R. solanacearum in the environment may have been previously underestimated.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant pathology 49 (2000), S. 0 
    ISSN: 1365-3059
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant pathology 49 (2000), S. 0 
    ISSN: 1365-3059
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: The sensitivity and specificity of various methods were compared for routine detection of Ralstonia solanacearum in a sandy loam soil. Populations fewer than 102 CFU per g soil were detected by dilution plating on a modified semiselective medium (SMSA). In comparison, a tomato bioassay was shown consistently to detect populations at or greater than 7·5 × 105 CFU per g soil. An indirect enzyme-linked immunosorbent assay (ELISA) was as sensitive as the tomato bioassay, but detected as few as 104 CFU per g soil when the suspension was first incubated in SMSA broth prior to testing. Detection using a nested polymerase chain reaction (PCR) was equally as sensitive as that using culture on SMSA agar, but only when the infested soil sample was first enriched overnight in SMSA broth prior to the nested PCR. Longer incubation periods in SMSA broth also increased the sensitivity of pathogen detection using a conventional PCR method, permitting detection of as few as 102 CFU per g soil after 60 h enrichment in SMSA broth. When evaluated using naturally infected field soils in Nepal, isolation of R. solanacearum on SMSA was reliable only when pathogen populations were higher than those of saprophytic soilborne bacteria. As few as 5 × 102 CFU of R. solanacearum per g were recovered from naturally infested soil, whereas the sensitivity of indirect ELISA was 106 CFU g−1.
    Type of Medium: Electronic Resource
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