Long-term nitrogen addition affects the phylogenetic turnover of soil microbial community responding to moisture pulse

Sci Rep. 2017 Dec 13;7(1):17492. doi: 10.1038/s41598-017-17736-w.

Abstract

How press disturbance (long-term) influences the phylogenetic turnover of soil microbial communities responding to pulse disturbances (short-term) is not fully known. Understanding the complex connections between the history of environmental conditions, assembly processes and microbial community dynamics is necessary to predict microbial response to perturbation. We started by investigating phylogenetic spatial turnover (based on DNA) of soil prokaryotic communities after long-term nitrogen (N) deposition and temporal turnover (based on RNA) of communities responding to pulse by conducting short-term rewetting experiments. The results showed that moderate N addition increased ecological stochasticity and phylogenetic diversity. In contrast, high N addition slightly increased homogeneous selection and decreased phylogenetic diversity. Examining the system with higher phylogenetic resolution revealed a moderate contribution of variable selection across the whole N gradient. The moisture pulse experiment showed that high N soils had higher rates of phylogenetic turnover across short phylogenetic distances and significant changes in community compositions through time. Long-term N input history influenced spatial turnover of microbial communities, but the dominant community assembly mechanisms differed across different N deposition gradients. We further revealed an interaction between press and pulse disturbances whereby deterministic processes were particularly important following pulse disturbances in high N soils.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Biodiversity
  • Nitrogen* / chemistry
  • Nitrogen* / metabolism
  • Phylogeny
  • RNA, Ribosomal, 16S
  • Soil / chemistry
  • Soil Microbiology*
  • Spatio-Temporal Analysis
  • Water* / chemistry
  • Water* / metabolism

Substances

  • RNA, Ribosomal, 16S
  • Soil
  • Water
  • Nitrogen