4.6 Article

Host identity is a dominant driver of mycorrhizal fungal community composition during ecosystem development

期刊

NEW PHYTOLOGIST
卷 205, 期 4, 页码 1565-1576

出版社

WILEY
DOI: 10.1111/nph.13226

关键词

arbuscular mycorrhizal fungal succession; ecosystem progression; ecosystem retrogression; long-term chronosequence; pyrosequencing; soil nutrient gradients; terminal restriction fragment length polymorphism (T-RFLP)

资金

  1. New Zealand Ministry of Business, Innovation and Employment's Science and Innovation Group
  2. Landcare Research Hayward Post-doctoral Fellowship
  3. Rutherford Discovery Fellowship
  4. Bio-Protection Research Centre, Lincoln University
  5. Antunes Plant and Soil Ecology Laboratory

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Little is known about the response of arbuscular mycorrhizal fungal communities to ecosystem development. We use a long-term soil chronosequence that includes ecosystem progression and retrogression to quantify the importance of host plant identity as a factor driving fungal community composition during ecosystem development. We identified arbuscular mycorrhizal fungi and plant species from 50 individual roots from each of 10 sites spanning 5-120000yr of ecosystem age using terminal restriction fragment length polymorphism (T-RFLP), Sanger sequencing and pyrosequencing. Arbuscular mycorrhizal fungal communities were highly structured by ecosystem age. There was strong niche differentiation, with different groups of operational taxonomic units (OTUs) being characteristic of early succession, ecosystem progression and ecosystem retrogression. Fungal alpha diversity decreased with ecosystem age, whereas beta diversity was high at early stages and lower in subsequent stages. A total of 39% of the variance in fungal communities was explained by host plant and site age, 29% of which was attributed to host and the interaction between host and site (24% and 5%, respectively). The strong response of arbuscular mycorrhizal fungi to ecosystem development appears to be largely driven by plant host identity, supporting the concept that plant and fungal communities are tightly coupled rather than independently responding to habitat.

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