Literature DB >> 16317037

High apoplastic solute concentrations in leaves alter water relations of the halophytic shrub, Sarcobatus vermiculatus.

J J James1, N N Alder, K H Mühling, A E Läuchli, K A Shackel, L A Donovan, J H Richards.   

Abstract

Predawn plant water potential (Psi(w)) is used to estimate soil moisture available to plants because plants are expected to equilibrate with the root-zone Psi(w). Although this equilibrium assumption provides the basis for interpreting many physiological and ecological parameters, much work suggests predawn plant Psi(w) is often more negative than root-zone soil Psi(w). For many halophytes even when soils are well-watered and night-time shoot and root water loss eliminated, predawn disequilibrium (PDD) between leaf and soil Psi(w) can exceed 0.5 MPa. A model halophyte, Sarcobatus vermiculatus, was used to test the predictions that low predawn solute potential (Psi(s)) in the leaf apoplast is a major mechanism driving PDD and that low Psi(s) is due to high Na+ and K+ concentrations in the leaf apoplast. Measurements of leaf cell turgor (Psi(p)) and solute potential (Psi(s)) of plants grown under a range of soil salinities demonstrated that predawn symplast Psi(w) was 1.7 to 2.1 MPa more negative than predawn xylem Psi(w), indicating a significant negative apoplastic Psi(s). Measurements on isolated apoplastic fluid indicated that Na+ concentrations in the leaf apoplast ranged from 80 to 230 mM, depending on salinity, while apoplastic K+ remained around 50 mM. The water relations measurements suggest that without a low apoplastic Psi(s), predawn Psi(p) may reach pressures that could cause cell damage. It is proposed that low predawn apoplastic Psi(s) may be an efficient way to regulate Psi(p) in plants that accumulate high concentrations of osmotica or when plants are subject to fluctuating patterns of soil water availability.

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Year:  2005        PMID: 16317037     DOI: 10.1093/jxb/erj016

Source DB:  PubMed          Journal:  J Exp Bot        ISSN: 0022-0957            Impact factor:   6.992


  6 in total

Review 1.  Nighttime stomatal conductance and transpiration in C3 and C4 plants.

Authors:  Mairgareth A Caird; James H Richards; Lisa A Donovan
Journal:  Plant Physiol       Date:  2007-01       Impact factor: 8.340

2.  Could vesicular transport of Na+ and Cl- be a feature of salt tolerance in halophytes?

Authors:  Timothy J Flowers; Edward P Glenn; Vadim Volkov
Journal:  Ann Bot       Date:  2019-01-01       Impact factor: 4.357

Review 3.  Sodium chloride toxicity and the cellular basis of salt tolerance in halophytes.

Authors:  Timothy J Flowers; Rana Munns; Timothy D Colmer
Journal:  Ann Bot       Date:  2014-12-01       Impact factor: 4.357

4.  Modeling the hydraulics of root growth in three dimensions with phloem water sources.

Authors:  Brandy S Wiegers; Angela Y Cheer; Wendy K Silk
Journal:  Plant Physiol       Date:  2009-06-19       Impact factor: 8.340

5.  Effect of saline water on seed germination and early seedling growth of the halophyte quinoa.

Authors:  M R Panuccio; S E Jacobsen; S S Akhtar; A Muscolo
Journal:  AoB Plants       Date:  2014-08-19       Impact factor: 3.276

6.  Growth performance, organ-level ionic relations and organic osmoregulation of Elaeagnus angustifolia in response to salt stress.

Authors:  Zhengxiang Liu; Jianfeng Zhu; Xiuyan Yang; Haiwen Wu; Qi Wei; Hairong Wei; Huaxin Zhang
Journal:  PLoS One       Date:  2018-01-23       Impact factor: 3.240

  6 in total

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