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  • 1
    Electronic Resource
    Electronic Resource
    Structure and function of the soil microbial community in microhabitats of a heavy metal polluted soil (2000)
    Springer
    Biology and fertility of soils 32 (2000), S. 390-400 
    Details
    ISSN: 1432-0789
    Keywords: Keywords Soil microbial biomass ; Soil enzymes ; Particle-size fractions ; Heavy metals ; Phospholipid fatty acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract  Particle-size fractionation of a heavy metal polluted soil was performed to study the influence of environmental pollution on microbial community structure, microbial biomass, microbial residues and enzyme activities in microhabitats of a Calcaric Phaeocem. In 1987, the soil was experimentally contaminated with four heavy metal loads: (1) uncontaminated controls; (2) light (300 ppm Zn, 100 ppm Cu, 50 ppm Ni, 50 ppm V and 3 ppm Cd); (3) medium; and (4) heavy pollution (two- and threefold the light load, respectively). After 10 years of exposure, the highest concentrations of microbial ninhydrin-reactive nitrogen were found in the clay (2–0.1 μm) and silt fractions (63–2 μm), and the lowest were found in the coarse sand fraction (2,000–250 μm). The phospholipid fatty acid analyses (PLFA) and denaturing gradient gel electrophoresis (DGGE) separation of 16S rRNA gene fragments revealed that the microbial biomass within the clay fraction was predominantly due to soil bacteria. In contrast, a high percentage of fungal-derived PLFA 18 : 2ω6 was found in the coarse sand fraction. Bacterial residues such as muramic acid accumulated in the finer fractions in relation to fungal residues. The fractions also differed with respect to substrate utilization: Urease was located mainly in the 〈2 μm fraction, alkaline phosphatase and arylsulfatase in the 2–63 μm fraction, and xylanase activity was equally distributed in all fractions. Heavy metal pollution significantly decreased the concentration of ninhydrin-reactive nitrogen of soil microorganisms in the silt and clay fraction and thus in the bulk soil. Soil enzyme activity was reduced significantly in all fractions subjected to heavy metal pollution in the order arylsulfatase 〉phosphatase 〉urease 〉xylanase. Heavy metal pollution did not markedly change the similarity pattern of the DGGE profiles and amino sugar concentrations. Therefore, microbial biomass and enzyme activities seem to be more sensitive than 16S rRNA gene fragments and microbial amino-sugar-N to heavy metal treatment.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s003740000268
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  • 2
    Electronic Resource
    Electronic Resource
    Impact of pasture contamination by copper, chromium, and arsenic timber preservative on soil microbial properties and nematodes (1994)
    Springer
    Biology and fertility of soils 18 (1994), S. 71-79 
    Details
    ISSN: 1432-0789
    Keywords: Heavy metals ; Microbial biomass ; Respiration ; Enzymes ; Denitrification ; Dimethyl sulphoxide reduction ; Nematodes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Microbial properties and nematode abundance were measured along a gradient of increasing Cu, Cr, and As concentrations (50–1300 mg Cr kg-1) in the top 5 cm of a pasture soil contaminated by runoff of preserving liquor from an adjacent timber-treatment plant. Microbial biomass C and N were significantly (P〈0.05) lower in contaminated than uncontaminated soils. The amount of microbial biomass C as a percentage of total organic C declined significantly (r 2 value with Cr 0.726*) with increasing contamination, and the ratio of respired C to biomass C was significantly (P〈0.05) higher with contamination. Substrate-induced respiration, microbial biomass P, and denitrification declined (r2 value with Cr 0.601, 0.833*, and 0.709*, respectively) with increasing contamination. Increasing contamination had no effect on prokaryote substrate-induced respiration but eukaryote: eukaryote substrate-induced respiration declined significantly (r 2 value with Cr 0.722*). Accordingly, the ratio of prokaryote substrate-induced respiration increased significantly (r 2 value with Cr 0.799*) with contamination. There was a significant (r 2 value with Cr 0.872*) hyperbolic relationship between sulphatase activity and contamination, with activity declining by approximately 80% at 〉1000 mg Cr kg-1. Increasing contamination had no effect on basal respiration, dimethyl sulphoxide reduction, and phosphatase, urease, and invertase activities. Numbers of plant-associated nematodes declined significantly (r 2 value with Cr 0.780*) with contamination. On a percentage basis, plant-feeding nematodes predominated in less contaminated soils, whereas bacterial-feeding and predatory nematodes predominated in heavily contaminated soils. The use of the fumigation—incubation procedure for measurement of microbial biomass C in heavy-metal contaminated soils is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00336448
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