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An ideal free distribution explains the root production of plants that do not engage in a tragedy of the commons game

McNickle, Gordon G., Brown, Joel S.·2014·Journal of Ecology

Published version of a preprint

Abstract

Summary: Below‐ground competition is intense and may dramatically reduce plant performance. However, there is still no consensus on the best strategies plants should use to maximize competitive ability in soil. Some suggest plants should grow roots according to nutrient availability, while others suggest plants should grow roots taking into account both nutrients and neighbours. Unambiguously, testing between these two alternative hypotheses has been challenging. This manuscript had three objectives. First, we presented a model of root growth under competition that is based on an ideal free distribution ( IFD ). Secondly, we develop the concept of the best response curve as a tool for clearer experimental tests of plant responses to neighbours. Thirdly, we test these ideas by growing fast cycling Brassica rapa either alone or with neighbours to examine this species' root growth strategy both alone and under competition. We hypothesize that those plants with no direct response to neighbours should grow roots according to an IFD . This means that if plants produce x roots in a soil volume of quality R, they should produce x / n roots in a soil volume of quality R / n . The experimental data were consistent with this prediction. Growing plants with neighbours was statistically identical to growing them with half as many nutrients. Thus, the only effect of neighbours was to reduce nutrient availability. This model provides an alternative to previous game theoretic models and suggests an experimental protocol based on the concept of the best response curve. We hope that testing the game theoretic model with a clear alternative model will guide experiment and debate. Synthesis . The data in the literature are mixed, with species sometimes responding to nutrients only, and sometimes responding interactively to both nutrients and neighbours. At present, we lack a general understanding of the causes or consequences of this diversity of strategies. We suggest that a greater understanding of trade‐offs among traits that are important for other biotic interactions (above‐ground competition, enemy defence, mutualisms) will lead to a greater understanding of why some species over‐proliferate roots when in competition but other species do not.

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Crossref · 10.1111/1365-2745.12259

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  • These three versions of IDMs have been applied to many different species and circumstances to develop predictions for how non-human and human organisms should distribute themselves across a landscape.

    “These three versions of ideal distribution models (IDMs) have been applied to many different species and circumstances to develop predictions for how non-human (Hendrickx, Palmer, and Travis 2013;McNickle and Brown 2014;Nicolai et al. 2014) and human (Disma, Sokolowski, and Tonneau 2011;Moritz et al. 2014aMoritz et al. , 2015Moritz et al. , 2014b;;Morris and Kingston 2002) organisms should”

    From The Ideal Distribution Model and Archaeological Settlement Patterning (2022) · cites this paper as McNickle and Brown 2014

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Metadata

Authors
McNickle, G. G., & Brown, J. S.
Affiliations
Department of Biological Sciences University of Illinois at Chicago 845 W. Taylor St. (MC066) Chicago IL 60607 USA
Venue
Journal of Ecology
Publisher
Wiley
Published
2014-05-07
Volume
102
Issue
4
Pages
963-971
ISSN
  • 0022-0477
  • 1365-2745
Cited by
60
References
0
Language
en
Funders
Natural Sciences and Engineering Research Council of Canada

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