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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Biology and fertility of soils 18 (1994), S. 109-114 
    ISSN: 1432-0789
    Keywords: Soil hydrogenase ; ATP ; Bacterial counts ; Particle size fractionation ; Cambisol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Low atmospheric H2 concentrations (0.55 ppmv) are oxidized in soils by a high-affinity activity with typical characteristics of an abiontic soil enzyme. This activity was measured in a meadow cambisol and a forest cambisol. In both soils, the maximum activity was reached at a soil moisture of about 20% water-holding capacity, and was localized in the top Ah horizon. The soils were fractionated by dry sieving and wet filtration into nine different particle-size fractions, ranging from 3 to 2000 μm in size. H2 oxidation was measured by three different assays and was compared to the ATP content and microscopic counts of bacteria in the same fractions. In the meadow soil, the specific activities of H2 oxidation increased with the particle size (maximum at 200–500 μm), whereas ATP and bacterial counts showed no trend. In the forest soil, the specific activities of H2 oxidation increased with the particle size up to 50–100 μm, and then decreased again. ATP and bacterial counts, however, showed the opposite trend, i.e., decreased with an increasing particle size. Thus the H2-oxidizing activity was not correlated with characteristic microbial biomass parameters. Although significant percentage (29–64%) of randomly isolated heterotrophic bacteria was able to oxidize H2, this activity was too small to account for the H2 oxidation in the soil. In both soils, most of the activity present was found in particles of 100–500 μm in size. The recovery shifted to smaller size fractions when larger soil aggregates were broken up by wet instead of dry sieving. Attempts to extract the H2-oxidizing activity from the soil particles were unsuccessful.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Biology and fertility of soils 12 (1991), S. 127-130 
    ISSN: 1432-0789
    Keywords: Soil hydrogenase ; Knallgas bacteria ; pH optimum ; Temperature optimum ; Apparent activation energy ; Seasonal change
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Hydrogen oxidation in soil was measured at low (1 ppmv) and high (300 ppmv) H2 concentrations to distinguish between the activities of abiontic soil hydrogenases and Knallgas bacteria, respectively. The two activities also showed distinctly different pH optima, temperature optima, and apparent activation energies. The pH optima for the soil hydrogenase activities were similar to the soil pH in situ, i.e., pH 8 in an slightly alkaline garden soil (pH 7.3) and pH 5 in an acidic cambisol (pH 4.6–5.4). Most probable number determinations in the alkaline acidic soils showed that Knallgas bacterial populations grew preferentially in neutral or acidic media, respectively. However, H2 oxidation activity by Knallgas bacteria in the acidic soil showed two distinct pH optima, one at pH 4 and a second at pH 6.4–7.0. The soil hydrogenase activities exhibited temperature optima at 35–40°C, whereas the Knallgas bacteria had optima at 50–60°C. The apparent activation energies of the soil hydrogenases were lower (11–23kJ mol-1) than those of the Knallgas bacteria (51–145 kJ mol-1). Most of the soil hydrogenase activity was located in the upper 10 cm of the acidic cambisol and changed with season. The seasonal activity changes were correlated with changes in soil moisture and soil pH.
    Type of Medium: Electronic Resource
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