Impact of wheat straw decomposition on successional patterns of soil microbial community structure

By F. Bastián, L. Bouziri, B. Nicolardot, L. Ranjard. 2009

402 citations recorded by the source corpus.

Subfields: Ecology, Plant Science, Soil Science

View Paper: https://www.semanticscholar.org/paper/b40027698891804b38b68f7dc512bdff95316df4

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Citations in the corpus

Effects of straw amendment and moisture on microbial communities in Chinese fluvo-aquic soil (2014, methodology): “…of straw amendment on eukaryotic community structure using some traditional methods, such as applying polymerase chain reaction-denaturing gradient gel electrophoresis and sequencing (Cahyani et al. 2004; Sugano et al. 2007) and automated ribosomal intergenic spacer analysis (Bastian et al. 2009).”
The Role of Microbial Communities in the Formation and Decomposition of Soil Organic Matter (2010, background): “In general, early stages of decomposition (14–28 days after substrate addition) are governed by bacterial activity (Bastian et al. 2009).”
Substrate quality affects kinetics and catalytic efficiency of exo-enzymes in rhizosphere and detritusphere (2016, background): “The detritusphere is characterized by high concentrations of easily degradable C sources, particularly at the early stages of residue decomposition (Bastian et al., 2009; Poll et al., 2010).”
Microbial hotspots and hot moments in soil: Concept & review (2015, background): “rhizosphere are explained by prolonged release of labile organics from decaying litter (Bastian et al., 2009; Poll et al., 2010) and their relative recalcitrance (Table 1).”
Carbon use efficiency of microbial communities: stoichiometry, methodology and modelling. (2013, background): “…greater than predicted by the bulk C : N ratio of the litter either because nutrients are translocated from the surrounding environment (net immobilisation) or opportunistic microorganisms are selectively targeting low C : E substrates within the litter matrix (Allison 2005; Bastian et al. 2009).”
Microbial richness and composition independently drive soil multifunctionality (2017, background): “…previous studies suggesting that Actinobacteria contains a broad array of genes that allow the breakdown and utilization of recalcitrant organic compounds such as lignin, chitin and cellulose that can be used under stressful soil conditions (low carbon; Bastian et al., 2009; Trivedi et al., 2013).”
Consistent responses of soil microbial communities to elevated nutrient inputs in grasslands across the globe (2015, result): “Whereas original evidence for generalizations of these life history strategies across broad bacterial taxonomic groups was based on responses to labile C inputs (28, 44, 45), our results extend evidence for these ecological classifications to the direct or indirect bacterial responses to nutrient ad”
Survival of Fusarium graminearum, the causal agent of Fusarium head blight. A review (2012, background): “Compared with r-strategists, K-strategists have a slower growth rate, a better ability to degrade recalcitrant organic substances and better survival rates when resources are limited (Bastian et al. 2009).”
Dynamics of bacterial communities in relation to soil aggregate formation during the decomposition of 13C-labelled rice straw (2012, background): “pattern of microbial succession, where rapidly growing r-strategist organisms are replaced by slower growing K-strategist organisms in the latter stages of organic matter decomposition, has been previously described (Fierer et al., 2007; Bastian et al., 2009; Baumann et al., 2009; Lerch et al., 2011”