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Plant-soil feedbacks and mycorrhizal type influence temperate forest population dynamics

Science
13 Jan 2017
Vol 355, Issue 6321
pp. 181-184

Soil biota and plant diversity

Soil biota, including symbionts such as mycorrhizal fungi and nitrogen-fixing bacteria, as well as fungal and bacterial pathogens, affect terrestrial plant diversity and growth patterns (see the Perspective by van der Putten). Teste et al. monitored growth and survival in Australian shrubland plant species paired with soil biota from plants of the same species and from other plants that use different nutrient acquisition strategies. Plant-soil feedbacks appear to drive local plant diversity through interactions between the different types of plants and their associated soil biota. Bennett et al. studied plant-soil feedbacks in soil and seeds from 550 populations of 55 species of North American trees. Feedbacks ranged from positive to negative, depending on the type of mycorrhizal association, and were related to how densely the same species occurred in natural populations.
Science, this issue p. 134, p. 173; see also p. 181

Abstract

Feedback with soil biota is an important determinant of terrestrial plant diversity. However, the factors regulating plant-soil feedback, which varies from positive to negative among plant species, remain uncertain. In a large-scale study involving 55 species and 550 populations of North American trees, the type of mycorrhizal association explained much of the variation in plant-soil feedbacks. In soil collected beneath conspecifics, arbuscular mycorrhizal trees experienced negative feedback, whereas ectomycorrhizal trees displayed positive feedback. Additionally, arbuscular mycorrhizal trees exhibited strong conspecific inhibition at multiple spatial scales, whereas ectomycorrhizal trees exhibited conspecific facilitation locally and less severe conspecific inhibition regionally. These results suggest that mycorrhizal type, through effects on plant-soil feedbacks, could be an important contributor to population regulation and community structure in temperate forests.

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Supplementary Material

Summary

Materials and Methods
Figs. S1 to S4
Table S1 to S5
References (2947)
Data S1

Resources

File (bennett-sm.pdf)
File (bennett_aai8212_database-s1.xlsx)

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Published In

Science
Volume 355 | Issue 6321
13 January 2017

Submission history

Received: 16 August 2016
Accepted: 25 November 2016
Published in print: 13 January 2017

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Acknowledgments

We thank the Natural Sciences and Engineering Research Council (NSERC) of Canada (Discovery Grant, and Discovery Accelerator Award) for financial support. J.A.B. was supported by a NSERC postdoctoral fellowship. Y.L. was supported by MPG Ranch (http://mpgranch.com). We also thank K. Botev, J. Coughlin, A. Dunger, L. Evans, J. Hale, M. Hemley, R. Juliano, H. King, L. Kunze, Y. Ling, W. Liou, E. Mason, M. Murata, J. Newton, H. Singh, M. Thompson, K. Ralph, and P. Veloso for field and laboratory assistance. Data have been uploaded as supplementary materials.

Authors

Affiliations

Jonathan A. Bennett* [email protected]
Department of Biology, University of British Columbia–Okanagan Campus, Kelowna, BC V1V 1V7, Canada.
Hafiz Maherali
Department of Integrative Biology, University of Guelph, Guelph, ON N1G 2W1, Canada.
Kurt O. Reinhart
Fort Keogh Livestock and Range Research Laboratory, U.S. Department of Agriculture–Agricultural Research Service, 243 Fort Keogh Road, Miles City, MT 59301–4016, USA.
Ylva Lekberg
MPG Ranch, Missoula, MT 59801, USA.
Department of Ecosystem and Conservation Sciences, University of Montana, Missoula, MT 59812, USA.
Miranda M. Hart
Department of Biology, University of British Columbia–Okanagan Campus, Kelowna, BC V1V 1V7, Canada.
John Klironomos* [email protected]
Department of Biology, University of British Columbia–Okanagan Campus, Kelowna, BC V1V 1V7, Canada.

Notes

*
Corresponding author. Email: [email protected] (J.A.B.); [email protected] (J.K.)

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