Abstract

The pull of water from the soil to the leaves causes water in the transpiration stream to be under negative pressure decreasing the water potential below zero. The osmotic concentration also contributes to the decrease in leaf water potential but with much lesser extent. Thus, the surface tension force is approximately balanced by a force induced by negative water potential resulting in concavely curved water-air interfaces in leaves. The lowered water potential causes a reduction in the equilibrium water vapor pressure in internal (sub-stomatal/intercellular) cavities in relation to that over water with the potential of zero, i.e., over the flat surface. The curved surface causes a reduction also in the equilibrium vapor pressure of dissolved CO2, thus enhancing its physical solubility to water. Although the water vapor reduction is acknowledged by plant physiologists its consequences for water vapor exchange at low water potential values have received very little attention. Consequences of the enhanced CO2 solubility to a leaf water-carbon budget have not been considered at all before this study. We use theoretical calculations and modeling to show how the reduction in the vapor pressures affects transpiration and carbon assimilation rates. Our results indicate that the reduction in vapor pressures of water and CO2 could enhance plant water use efficiency up to about 10% at a leaf water potential of −2 MPa, and much more when water potential decreases further. The low water potential allows for a direct stomatal water vapor uptake from the ambient air even at sub-100% relative humidity values. This alone could explain the observed rates of foliar water uptake by e.g., the coastal redwood in the fog belt region of coastal California provided the stomata are sufficiently open. The omission of the reduction in the water vapor pressure causes a bias in the estimates of the stomatal conductance and leaf internal CO2 concentration based on leaf gas exchange measurements. Manufactures of leaf gas exchange measurement systems should incorporate leaf water potentials in measurement set-ups.

Highlights

  • Water potential is negative in the xylem of virtually all terrestrial plants (Pockman et al, 1995)

  • We demonstrate that water uptake in vapor form by reverse transpiration would be theoretically sufficient to explain the observed rates of foliar water uptake in coastal redwood trees

  • Our theoretical calculations demonstrate that the decrease in vapor pressure in the sub-stomatal cavity in the leaves due to negative water potential has a significant role in plant leaf gas exchange

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Summary

Introduction

Water potential is negative in the xylem of virtually all terrestrial plants (Pockman et al, 1995). Water potential is lowered by transpiration from the leaves assisted by the cohesive forces between water molecules causing water to be under tension, i.e., under negative pressure. According to Young-Laplace’s formula (e.g., Nobel, 2005), the cohesive forces are balanced by the surface tension and the balance is manifested as curved, concave airwater surfaces in leaves. The higher the tension is, i.e., the lower the water potential, the stronger the concavity is. Solutes dissolved in the xylem sap may contribute to the decrease in xylem water potential. The osmotic component of water potential in the apoplastic water is marginal since the amount of dissolved solutes in the apoplast is typically very small (Nobel, 2005) and we ignore the osmotic effect here

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