The effect of agricultural land use change on soil microbial community composition and biomass remains a widely debated topic. Here, we investigated soil microbial community composition and biomass [e.g., bacteria (B), fungi (F), Arbuscular mycorrhizal fungi (AMF) and Actinomycete (ACT)] using phospholipid fatty acids (PLFAs) analysis, and basal microbial respiration in afforested, cropland and...

In many microbial bioreactors, high shear rates result in strong attachment of microbes and dense biofilms. In this study, high shear rates were applied to enrich an anodophilic microbial consortium in a microbial fuel cell (MFC). Enrichment at a shear rate of about 120 s(-1) resulted in the production of a current and power output two to three times higher than those in the case of low shear r...

The food source of sediment-ingesting animals is a subject of controversy, centering on the notion that the microbial biomass in sediments is insufficient to support caloric need. Gizzard shad Dorosoma cepedianum are omnivorous, sediment-ingesting fish that frequently impact the trophic structure of temperate lake and reservoir food webs. Prior gut content analyses of this fish have typically d...

The long term effect of biochar application on soil microbial biomass is not well understood. We measured soil microbial biomass carbon (MBC) and nitrogen (MBN) in a field experiment during a winter wheat growing season after four consecutive years of no (CK), 4.5 (B4.5) and 9.0 t biochar ha(-1) yr(-1) (B9.0) applied. For comparison, a treatment with wheat straw residue incorporation (SR) was a...

In many terrestrial ecosystems plant productivity is limited by the availability of mineral nitrogen, which is produced by soil microbial transformations of organic N in soil organic matter (SOM-N). Mineral N availability results from two opposing processes, 1) gross mineral N production (gross ammonification/ gross nitrification) and 2) microbial N immobilization. These processes can be influe...

The patterns and drivers of soil microbial communities in forest plantations remain inadequate although they have been extensively studied in natural forest and grassland ecosystems. In this study, using data from 12 subtropical plantation sites, we found that the overstory tree biomass and tree cover increased with increasing plantation age. However, there was a decline in the aboveground biom...

The dispersion of soilborne plant pathogens could be greater in closed soilless growing systems than in open ones. The effect of three soilless growing systems (open, closed and closed with slow sand filtration) on the dispersion of Verticillium dahliae propagules and the severity of the disease in strawberry (Fragaria × ananassa Duch.) has been analysed. V. dahliae dispersion in a closed syste...

This paper reviews the current knowledge of microbial processes affecting C sequestration in agroecosystems. The microbial contribution to soil C storage is directly related to microbial community dynamics and the balance between formation and degradation of microbial byproducts. Soil microbes also indirectly influence C cycling by improving soil aggregation, which physically protects soil orga...

BACKGROUND Biomass has been studied as biomarker to evaluate the effect of heavy metals on microbial communities. Nevertheless, the most important methodological problem when working with natural and artificial microbial mats is the difficulty to evaluate changes produced on microorganism populations that are found in thicknesses of just a few mm depth. METHODOLOGY/PRINCIPAL FINDINGS Here, we...

Empirical studies show that nitrogen (N) addition often reduces microbial decomposition of soil organic matter (SOM) and carbon dioxide (CO2) production via microbial respiration. Although predictions from theoretical models support these findings, the mechanisms that drive this response remain unclear. To address this uncertainty, we sampled soils of three grassland sites in the U.S. Central G...