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Interspecific Plant Interactions Reflected in Soil Bacterial Community Structure and Nitrogen Cycling in Primary Succession

Joseph E. KnelmanInstitute of Arctic and Alpine Research, University of Colorado Boulder, Boulder, CO, United StatesEmily GrahamPacific Northwest National Laboratory (U.S. Department of Energy), Richland, WA, United StatesJanet S. PrevéyPacific Northwest Research Station, The United States Forest Service, Olympia, WA, United StatesMichael S. RobesonDepartment of Biomedical Informatics, University of Arkansas for Medical Sciences, Little Rock, AR, United StatesPatrick H. KellyInstitute of Arctic and Alpine Research, University of Colorado Boulder, Boulder, CO, United StatesEran HoodDepartment of Natural Sciences, University of Alaska Southeast, Juneau, AK, United StatesSteven K. SchmidtDepartment of Ecology and Evolutionary Biology, University of Colorado Boulder, Boulder, CO, United States
2018en
ABI

Аннотация

Past research demonstrating the importance plant-microbe interactions as drivers of ecosystem succession has focused on how plants condition soil microbial communities, impacting subsequent plant performance and plant community assembly. These studies, however, largely treat microbial communities as a black box. In this study we sought to examine how emblematic shifts from early-successional Alnus sinuata (alder) to late successional Picea sitchensis (spruce) in primary succession may be reflected in specific belowground changes in bacterial community structure and nitrogen cycling related to the interaction of these two plants. We examined early successional alder-conditioned soils in a glacial forefield to delineate how alders alter the soil microbial community with increasing dominance. Further, we assessed the impact of late-successional spruce plants on these early-successional alder-conditioned microbiomes and related nitrogen cycling through a leachate addition microcosm experiment. In total, we show how increasingly abundant alder select for particular bacterial taxa. Additionally, we found that spruce leachate significantly alters the composition of these microbial communities in large part by driving declines in taxa that are enriched by alder, including bacterial symbionts. We found these effects to be spruce-specific, beyond a general leachate effect. Our work also demonstrates a unique influence of spruce on ammonium availability. Such insights bolster theory relating the importance of plant-microbe interactions with late-successional plants and interspecific plant interactions more generally.

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