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3D deformation field in growing plant roots reveals both mechanical and biological responses to axial mechanical forces

Strong regions and physical barriers in soils may slow root elongation, leading to reduced water and nutrient uptake and decreased yield. In this study, the biomechanical responses of roots to axial mechanical forces were assessed by combining 3D live imaging, kinematics and a novel mechanical senso...

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Autores principales: Bizet, François, Bengough, A. Glyn, Hummel, Irène, Bogeat-Triboulot, Marie-Béatrice, Dupuy, Lionel X.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066484/
https://www.ncbi.nlm.nih.gov/pubmed/27664958
http://dx.doi.org/10.1093/jxb/erw320
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author Bizet, François
Bengough, A. Glyn
Hummel, Irène
Bogeat-Triboulot, Marie-Béatrice
Dupuy, Lionel X.
author_facet Bizet, François
Bengough, A. Glyn
Hummel, Irène
Bogeat-Triboulot, Marie-Béatrice
Dupuy, Lionel X.
author_sort Bizet, François
collection PubMed
description Strong regions and physical barriers in soils may slow root elongation, leading to reduced water and nutrient uptake and decreased yield. In this study, the biomechanical responses of roots to axial mechanical forces were assessed by combining 3D live imaging, kinematics and a novel mechanical sensor. This system quantified Young’s elastic modulus of intact poplar roots (32MPa), a rapid <0.2 mN touch-elongation sensitivity, and the critical elongation force applied by growing roots that resulted in bending. Kinematic analysis revealed a multiphase bio-mechanical response of elongation rate and curvature in 3D. Measured critical elongation force was accurately predicted from an Euler buckling model, indicating that no biologically mediated accommodation to mechanical forces influenced bending during this short period of time. Force applied by growing roots increased more than 15-fold when buckling was prevented by lateral bracing of the root. The junction between the growing and the mature zones was identified as a zone of mechanical weakness that seemed critical to the bending process. This work identified key limiting factors for root growth and buckling under mechanical constraints. The findings are relevant to crop and soil sciences, and advance our understanding of root growth in heterogeneous structured soils.
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spelling pubmed-50664842016-10-18 3D deformation field in growing plant roots reveals both mechanical and biological responses to axial mechanical forces Bizet, François Bengough, A. Glyn Hummel, Irène Bogeat-Triboulot, Marie-Béatrice Dupuy, Lionel X. J Exp Bot Research Paper Strong regions and physical barriers in soils may slow root elongation, leading to reduced water and nutrient uptake and decreased yield. In this study, the biomechanical responses of roots to axial mechanical forces were assessed by combining 3D live imaging, kinematics and a novel mechanical sensor. This system quantified Young’s elastic modulus of intact poplar roots (32MPa), a rapid <0.2 mN touch-elongation sensitivity, and the critical elongation force applied by growing roots that resulted in bending. Kinematic analysis revealed a multiphase bio-mechanical response of elongation rate and curvature in 3D. Measured critical elongation force was accurately predicted from an Euler buckling model, indicating that no biologically mediated accommodation to mechanical forces influenced bending during this short period of time. Force applied by growing roots increased more than 15-fold when buckling was prevented by lateral bracing of the root. The junction between the growing and the mature zones was identified as a zone of mechanical weakness that seemed critical to the bending process. This work identified key limiting factors for root growth and buckling under mechanical constraints. The findings are relevant to crop and soil sciences, and advance our understanding of root growth in heterogeneous structured soils. Oxford University Press 2016-10 2016-09-24 /pmc/articles/PMC5066484/ /pubmed/27664958 http://dx.doi.org/10.1093/jxb/erw320 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Bizet, François
Bengough, A. Glyn
Hummel, Irène
Bogeat-Triboulot, Marie-Béatrice
Dupuy, Lionel X.
3D deformation field in growing plant roots reveals both mechanical and biological responses to axial mechanical forces
title 3D deformation field in growing plant roots reveals both mechanical and biological responses to axial mechanical forces
title_full 3D deformation field in growing plant roots reveals both mechanical and biological responses to axial mechanical forces
title_fullStr 3D deformation field in growing plant roots reveals both mechanical and biological responses to axial mechanical forces
title_full_unstemmed 3D deformation field in growing plant roots reveals both mechanical and biological responses to axial mechanical forces
title_short 3D deformation field in growing plant roots reveals both mechanical and biological responses to axial mechanical forces
title_sort 3d deformation field in growing plant roots reveals both mechanical and biological responses to axial mechanical forces
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066484/
https://www.ncbi.nlm.nih.gov/pubmed/27664958
http://dx.doi.org/10.1093/jxb/erw320
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