Abstract

<p>The pathways of water across root tissues and their relative contribution to plant water uptake remain debated. This is mainly due to technical challenges in measuring water flux non-invasively at the cellular scale under realistic conditions.  We developed a new method to quantify water fluxes inside roots growing in soils. The method combines spatiotemporal quantification of deuterated water distribution imaged by rapid neutron tomography with an inverse simulation of water transport across root tissues. Using this non-invasive technique, we estimated for the first time the in-situ radial water fluxes [m s<sup>-1</sup>] in apoplastic and cell-to-cell pathways. The water flux in the apoplast of twelve days-old lupins (Lupinus albus L. cv. Feodora) was seventeen times faster than in the cell-to-cell pathway. Hence, the overall contribution of the apoplast in water flow [m<sup>3</sup> s<sup>-1</sup>] across the cortex is, despite its small volume of 5%, as large as 57±8 % (Mean ± SD for n=3) of the total water flow. This method is suitable to non-invasively measure the response of cellular scale root hydraulics and water fluxes to varying soil and climate conditions.</p>

Highlights

  • The pathways of water across root tissues and their relative contribution to plant water uptake remain debated

  • The gradients were steeper during nighttime than daytime indicating that the presence of an endodermis significantly limited the transport of D2O across root tissue at night, while its effect was less pronounced during daytime measurements

  • Rapid neutron tomography was used to in-situ trace the transport of D2O in roots

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Summary

Introduction

The pathways of water across root tissues and their relative contribution to plant water uptake remain debated. The method combines spatiotemporal quantification of deuterated water distribution imaged by rapid neutron tomography with an inverse simulation of water transport across root tissues Using this non-invasive technique, we estimated for the first time the in-situ radial water fluxes [m s−1] in apoplastic and cell-to-cell pathways. The overall contribution of the apoplast in water flow [m3 s−1] across the cortex is, despite its small volume of 5%, as large as 57 ± 8% (Mean ± SD for n = 3) of the total water flow This method is suitable to noninvasively measure the response of cellular scale root hydraulics and water fluxes to varying soil and climate conditions. Some studies claimed that the apoplastic barriers are imperfect and have a varying degree of interruption depending on plant species, developmental stages and growth condition[22–24] Both pathways appear possible, but their relative contributions remain unanswered. Detailed time-series neutron tomographs are shown as Supplementary Information

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