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. 1997 Mar;113(3):881–893. doi: 10.1104/pp.113.3.881

Growth, Water Relations, and Accumulation of Organic and Inorganic Solutes in Roots of Maize Seedlings during Salt Stress.

H G Rodriguez 1, JKM Roberts 1, W R Jordan 1, M C Drew 1
PMCID: PMC158208  PMID: 12223650

Abstract

Seedlings of maize (Zea mays L. cv Pioneer 3906), hydroponically grown in the dark, were exposed to NaCl either gradually (salt acclimation) or in one step (salt shock). In the salt-acclimation treatment, root extension was indistinguishable from that of unsalinized controls for at least 6 d at concentrations up to 100 mM NaCl. By contrast, salt shock rapidly inhibited extension, followed by a gradual recovery, so that by 24 h extension rates were the same as for controls, even at 150 mM NaCl. Salt shock caused a rapid decrease in root water and solute potentials for the apical zones, and the estimated turgor potential showed only a small decline; similar but more gradual changes occurred with salt acclimation. The 5-bar decrease in root solute potential with salt shock (150 mM NaCl) during the initial 10 min of exposure could not be accounted for by dehydration, indicating that substantial osmotic adjustment occurred rapidly. Changes in concentration of inorganic solutes (Na+, K+, and Cl-) and organic solutes (proline, sucrose, fructose, and glucose) were measured during salt shock. The contribution of these solutes to changes in root solute potential with salinization was estimated.

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Selected References

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  1. Azaizeh H., Gunse B., Steudle E. Effects of NaCl and CaCl(2) on Water Transport across Root Cells of Maize (Zea mays L.) Seedlings. Plant Physiol. 1992 Jul;99(3):886–894. doi: 10.1104/pp.99.3.886. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Azaizeh H., Steudle E. Effects of Salinity on Water Transport of Excised Maize (Zea mays L.) Roots. Plant Physiol. 1991 Nov;97(3):1136–1145. doi: 10.1104/pp.97.3.1136. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Binzel M. L., Hess F. D., Bressan R. A., Hasegawa P. M. Intracellular compartmentation of ions in salt adapted tobacco cells. Plant Physiol. 1988 Feb;86(2):607–614. doi: 10.1104/pp.86.2.607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chang K., Roberts J. K. Observation of Cytoplasmic and Vacuolar Malate in Maize Root Tips by C-NMR Spectroscopy. Plant Physiol. 1989 Jan;89(1):197–203. doi: 10.1104/pp.89.1.197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Ferguson J. E., Dickinson D. B., Rhodes A. M. Analysis of Endosperm Sugars in a Sweet Corn Inbred (Illinois 677a) Which Contains the Sugary Enhancer (se) Gene and Comparison of se with Other Corn Genotypes. Plant Physiol. 1979 Mar;63(3):416–420. doi: 10.1104/pp.63.3.416. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Frensch J., Hsiao T. C. Transient Responses of Cell Turgor and Growth of Maize Roots as Affected by Changes in Water Potential. Plant Physiol. 1994 Jan;104(1):247–254. doi: 10.1104/pp.104.1.247. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Joly R. J. Effects of sodium chloride on the hydraulic conductivity of soybean root systems. Plant Physiol. 1989 Dec;91(4):1262–1265. doi: 10.1104/pp.91.4.1262. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Kurth E., Cramer G. R., Läuchli A., Epstein E. Effects of NaCl and CaCl(2) on Cell Enlargement and Cell Production in Cotton Roots. Plant Physiol. 1986 Dec;82(4):1102–1106. doi: 10.1104/pp.82.4.1102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. McNulty I. B. Rapid osmotic adjustment by a succulent halophyte to saline shock. Plant Physiol. 1985 May;78(1):100–103. doi: 10.1104/pp.78.1.100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Neumann P. M., Van Volkenburgh E., Cleland R. E. Salinity stress inhibits bean leaf expansion by reducing turgor, not wall extensibility. Plant Physiol. 1988;88:233–237. doi: 10.1104/pp.88.1.233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Roberts J. K., Hooks M. A., Miaullis A. P., Edwards S., Webster C. Contribution of Malate and Amino Acid Metabolism to Cytoplasmic pH Regulation in Hypoxic Maize Root Tips Studied Using Nuclear Magnetic Resonance Spectroscopy. Plant Physiol. 1992 Feb;98(2):480–487. doi: 10.1104/pp.98.2.480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Sharp R. E., Silk W. K., Hsiao T. C. Growth of the maize primary root at low water potentials : I. Spatial distribution of expansive growth. Plant Physiol. 1988 May;87(1):50–57. doi: 10.1104/pp.87.1.50. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Voetberg G. S., Sharp R. E. Growth of the Maize Primary Root at Low Water Potentials : III. Role of Increased Proline Deposition in Osmotic Adjustment. Plant Physiol. 1991 Aug;96(4):1125–1130. doi: 10.1104/pp.96.4.1125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. de Leon-Casasola O. A., Lema M. J. Epidural bupivacaine/sufentanil therapy for postoperative pain control in patients tolerant to opioid and unresponsive to epidural bupivacaine/morphine. Anesthesiology. 1994 Feb;80(2):303–309. doi: 10.1097/00000542-199402000-00010. [DOI] [PubMed] [Google Scholar]

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