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H. Wiebe (1966)
Matric potential of several plant tissues and biocolloids.Plant physiology, 41 9
(1964)
Ion absorption by shoot tissue: Kinetics of K and Rb absorption by corn leaf tissue
John Boyer (1967)
Matric potentials of leaves.Plant physiology, 42 2
E. Macrobbie, Ai~d Dainty (1958)
ION TRANSPORT IN NITELLOPSIS OBTUSAThe Journal of General Physiology, 42
J. Wilson, C. Rose (1967)
The Components of Leaf Water Potential I. Osmotic and Matric PotentialsAustralian Journal of Biological Sciences, 20
(1969)
A method for determining solutes in the cell walls of leaves
(1964)
Extracellular salt accumulation , a possible mechanism of salt injury in plants
Richard Smith, Emanuel Epstein (1964)
Ion Absorption by Shoot Tissue: Technique and First Findings with Excised Leaf Tissue of Corn.Plant physiology, 39 3
D. Thorne (1954)
Diagnosis and Improvement of Saline and Alkali SoilsAgronomy Journal, 46
L. Bernstein (1961)
OSMOTIC ADJUSTMENT OF PLANTS TO SALINE MEDIA. I. STEADY STATEAmerican Journal of Botany, 48
Richard Smith, E. Epstein (1964)
Ion Absorption by Shoot Tissue: Kinetics of Potassium and Rubidium Absorption by Corn Leaf Tissue.Plant physiology, 39 6
J. Morgan, H. Tukey (1964)
Characterization of Leachate from Plant Foliage.Plant physiology, 39 4
(1958)
Loss of nutrients by foliar leaching as determined by radioisotopes
Abstract A perfusion method is described whereby large discs of amphistomatous leaves are vacuum-perfused with water so that either successive fractions of perfusate may be analyzed for solutes or the infused water may be displaced and collected after equilibration with the leaf cells. With castor bean leaves, estimates of electrolyte concentration in cell wall water by the two methods were similar. Total electrolytes in leaf cell wall water of castor beans (Ricinus communis), sunflower (Helianthus annuus), and cabbage (Brassica oleracea capitata) from nonsaline cultures were about 2, 2, and 10 milliequivalents per liter, respectively, increasing to 4, 10, and 30 milliequivalents per liter under saline conditions. Electrolytes recovered in successive fractions were similar in composition, and continuous perfusion resulted in a steady release of solutes, the concentration in the perfusate varying inversely with the perfusion rate. Diffusional release of solutes from cells was less than expected at low perfusion rates, suggesting that solute reabsorption may increase as solute concentration in the perfusate increases with decreased perfusion rates. Perfusate concentration and composition were essentially unaffected by temperature (2 and 23 C) or by perfusing with 0.5 mm CaSO4 rather than with water. Electrolytes in perfusates on an equivalent basis were Ca2+, 30%; Mg2+, 10%; and Na+ + K+, 60%, the proportions of sodium increasing from 10 to 50% in leaves (cabbage) that accumulated sodium under saline conditions. Salinity (added NaCl) of the root culture medium caused a 3- to 5-fold increase in total cell wall electrolyte concentration, but this amounted to an increase from less than 1 or a few per cent to no more than 7% (in cabbage) of the cell sap electrolyte concentrations. Solutes in the cell wall appear to be in dynamic equilibrium with intracellular solutes. This content is only available as a PDF. © 1971 American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)
Plant Physiology – Oxford University Press
Published: Mar 1, 1971
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