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. 2013 Sep 5:4:265.
doi: 10.3389/fmicb.2013.00265. eCollection 2013.

Controls on soil microbial community stability under climate change

Affiliations

Controls on soil microbial community stability under climate change

Franciska T de Vries et al. Front Microbiol. .

Abstract

Soil microbial communities are intricately linked to ecosystem functioning because they play important roles in carbon and nitrogen cycling. Still, we know little about how soil microbial communities will be affected by disturbances expected with climate change. This is a significant gap in understanding, as the stability of microbial communities, defined as a community's ability to resist and recover from disturbances, likely has consequences for ecosystem function. Here, we propose a framework for predicting a community's response to climate change, based on specific functional traits present in the community, the relative dominance of r- and K-strategists, and the soil environment. We hypothesize that the relative abundance of r- and K-strategists will inform about a community's resistance and resilience to climate change associated disturbances. We also propose that other factors specific to soils, such as moisture content and the presence of plants, may enhance a community's resilience. For example, recent evidence suggests microbial grazers, resource availability, and plant roots each impact on microbial community stability. We explore these hypotheses by offering three vignettes of published data that we re-analyzed. Our results show that community measures of the relative abundance of r- and K-strategists, as well as environmental properties like resource availability and the abundance and diversity of higher trophic levels, can contribute to explaining the response of microbial community composition to climate change-related disturbances. However, further investigation and experimental validation is necessary to directly test these hypotheses across a wide range of soil ecosystems.

Keywords: PLFA; bacteria; disturbance; drought; fungi; pyrosequencing; resilience; resistance.

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Figures

Figure 1
Figure 1
Case study 1: the presence of a plant increased the resilience of microbial community composition 77 days after ending the glasshouse-based drought [F(1, 24) = 15.7, P = 0.0005]. Resilience was greater in grassland than in wheat [F(1, 24) = 5.36, P = 0.029]; there were no interaction effects between land use or previous drought. Pairwise comparisons within land use and field drought treatments indicated that only within the wheat field drought treatment the treatments with and without plant were (marginally) significantly different (Tukey's HSD comparison, P = 0.059, indicated by an asterisk).
Figure 2
Figure 2
Framework for predicting microbial community response to climate change. The bottom part of the figure illustrates the necessity of characterizing and annotating specific functional genes (here conceptually represented by colored sequences) that code for microbial traits of importance for community responses for specific disturbances associated with climate change. Once known and annotated, these genes can inform about the relative abundance of a suite of genes that may underlie a community's response to climate change (arrow 1). The middle part designates the relative abundance of functional genes present in a community. This space is multidimensional and here we chose to visualize C cycling genes, N cycling genes, and drought resistance genes (see Table 1), but other known and unknown genes such as those involved in sporulation or specific dispersal mechanisms should be included. The functional genes present in a community may, or may not, have a relationship with the dominance of r- and K-strategists or with the community's environment (colored dots in middle and upper part). The role of specific functional genes in a community's response and their links with the r-K spectrum are yet to be elucidated (arrow 2). The upper part of the figure indicates a community's response to climate change, as determined by the relative abundance of r- and K-strategists and the community's environment (in this case nutrient availability, but this can be replaced by other environmental factors such as the abundance or richness of higher trophic levels). A K-strategist dominated microbial community in a nutrient-poor environment likely has high resistance, whereas an r-dominated community in a nutrient-rich environment likely has high resilience. The exact shape of the surface might vary depending on specific circumstances.

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