Abstract

The effects of plant species which frequently occur in set-aside arable land on rhizosphere soil properties were assessed and compared to rhizosphere soil of Secale cereale (Rye) grown on an intensively managed arable soil (sandy Cambisol, Saxony, NE- Germany). On a 6 year old set-aside arable land rhizosphere soil samples were taken under Agropyron repens, Cirsium arvense and Rumex acetosa, the most frequent plant species, and under the leguminous plant species Vicia villosa. Phospholipid fatty acid analysis (PLFA) has been used to characterise the structure of the soil microbial community. Carbon mineralisation rates as well as gross ( 15 N isotope pool dilution method) and net nitrogen mineralisation rates were determined as indicator of microbial activity. In intensive managed plots a rhizosphere effect was obvious in higher nutrient contents, gross N mineral- isation rates and higher relative abundances of fungi and protozoa in Rye rhizosphere compared to bulk soil. Plant species altered rhizosphere microbial activity. Lowest gross N mineralisation and gross NH4 con- sumption rates were detected in Rye rhizosphere soil. Both rates revealed high positive correlations with dissolved organic carbon (extracted with KCl) and soil pH. The rhizosphere soil microbial communities of the three dominant plant species of the set-aside arable land (Agropyron, Cirsium, Rumex) were more similar to each other than to Vicia grown on the same set-aside plots and Rye grown on intensive managed plots. The highest number of non-identified PLFAs detected in Vicia rhizosphere soil suggests that microbial diversity was highest. Differences in quantity and quality of Vicia rhizodeposition, especially higher N contents, seem to induce the higher microbial activity and different microbial community structure. The rhizo- sphere soil of the dominant plant species on the set- aside and intensively managed arable land reflected the differences in bulk soil properties (obtained in a previous study) between the two management systems (e.g. pH, gross N mineralisation, metabolic quotient, PLFA marker characteristic of Gbacteria and fungi).

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