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  • Articles: DFG German National Licenses  (2)
  • 1995-1999  (2)
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  • Articles: DFG German National Licenses  (2)
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  • 1
    ISSN: 1432-1939
    Keywords: Climax tree species ; Phosphorus Photosynthesis ; Pioneer tree species ; Tropical rainforest
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In Guyana dense rainforest occurs on intensely weathered acid soils, low in soil phosphorus. To investigate whether low P availability limits photosynthesis of trees growing on these soils more than N does, leaf P and N content, and their relationship with the photosynthetic capacity (A sat, μmol CO2 m-2 s-1) were studied for nine pioneer and climax tree species in a range of light climates. Light environment was described using hemispherical photographs. For both pioneer and climax species, leaf P content (r 2=0.71 and 0.23, respectively) is a more important determinant of A sat than leaf N content (r 2=0.54 and 0.12, respectively). Pioneer species have a higher leaf P and N content than climax species. At similar P or N content, pioneers have a higher A sat than climax species. The saplings studied had a relatively high A sat, considering their low P concentration (15–30 μmol P g-1). All species studied had a constant leaf P and N concentration and photosynthetic capacity across light climates, because specific leaf mass (g m-2) increased similarly with light availability. This acclimation to a change in light environment makes a possible limitation of A sat by P or N independent of light environment.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-2665
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Gaucher disease is the most frequent lysosomal storage disease in Greece, accounting for 24% of all lysosomal disorders diagnosed during the last 13 years at the Institute of Child Health in Athens. The nature of the defects in glucocerebrosidase in Greek Gaucher patients with non-neuronopathic (type 1) and neuronopathic (types 2 and 3) phenotypes was investigated at the level of the glucocerebrosidase gene and enzyme activity. Mutation analysis performed in 10/23 Gaucher patients with different types of the disorder led to the identification of four mutations, N370S, L444P, R463C and D409H, comprising 75% of the investigated alleles. N370S was only found in association with type 1 disease. The genotype D409H/R463C was identified for the first time and was associated with the severe type 2 disorder. There was no correlation between residualin vitro enzyme activity and either phenotype or genotype. However, in cultured fibroblasts of the neuronopathic cases, glucocerebrosidase protein concentration was reduced and the capacity to degrade exogenous C6NBD-glucosylceramide was more severely impaired.
    Type of Medium: Electronic Resource
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