Plant Physiology 48:631-636 (1971)
© 1971 American Society of Plant Biologists
Articles
Immediate and Subsequent Growth Responses of Maize Leaves to Changes in Water Status 1
Edmundo Acevedo2,
Theodore C. Hsiao and
D. W. Henderson
a Laboratory of Plant-Water Relations, Department of Water Science and Engineering, University of California, Davis, California 95616
Elongation of intact young leaves of maize was found to be dynamically dependent on soil water supply. With adequate water, elongation was remarkably constant but slowed when the water potential of the soil in pots dropped from 0.1 to 0.2 bar and stopped when it dropped to 2.5 bars. The corresponding range of leaf water potential was 2.8 to 7 bars. Elongation resumed in less than a few seconds after a mildly water-stressed plant was rewatered.
The effects on leaf elongation of step-wise changes in water potential of the root solution were determined. When the water potential of the root medium suddenly decreased below 0 bar, growth stopped initially and then resumed at a lower rate. When the water potential was suddenly increased back to 0 bar, growth accelerated transitorily to a high rate before slowing to the steady state rate. These results suggest an increase in cell extensibility during water stress.
Leaves stressed for 1 or more days attained after rewatering almost the length of the control leaves. Growth rate after rewatering did not exceed that of the control at the corresponding developmental stage except during the short transitory rapid phase lasting only a fraction of an hour.
As stress developed, growth stopped before carbon dioxide assimilation decreased noticeably. Upon the release of mild and short stress, the transitory rapid growth completely made up for the reduced elongation during stress, suggesting that metabolic processes for cell expansion might have proceeded unchecked during the stress period.
The sensitivity and rapidity of response to changes in water status all point to the direct role of water in growth; its uptake provides the physical force for cell enlargement.
2 Present address: Universidad de Chile, Departamento Produccion Agricola, Casilla 1004, Santiago, Chile.
1 This work was supported in part by Grant B-029-CAL from the Office of Water Resources Research, United States Department of Interior; by a grant from the Water Resources Center, University of California; and by National Science Foundation Grant GB 5658.
This article has been cited by other articles:

|
 |

|
 |
 
L. I. Solari and T. M. DeJong
The effect of root pressurization on water relations, shoot growth, and leaf gas exchange of peach (Prunus persica) trees on rootstocks with differing growth potential and hydraulic conductance
J. Exp. Bot.,
June 1, 2006;
57(9):
1981 - 1989.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
W. Fricke, G. Akhiyarova, W. Wei, E. Alexandersson, A. Miller, P. O. Kjellbom, A. Richardson, T. Wojciechowski, L. Schreiber, D. Veselov, et al.
The short-term growth response to salt of the developing barley leaf
J. Exp. Bot.,
March 1, 2006;
57(5):
1079 - 1095.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
W. Fricke, G. Akhiyarova, D. Veselov, and G. Kudoyarova
Rapid and tissue-specific changes in ABA and in growth rate in response to salinity in barley leaves
J. Exp. Bot.,
May 1, 2004;
55(399):
1115 - 1123.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
W. FRICKE
Biophysical Limitation of Cell Elongation in Cereal Leaves
Ann. Bot.,
August 1, 2002;
90(2):
157 - 167.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
W. Fricke and W. S. Peters
The Biophysics of Leaf Growth in Salt-Stressed Barley. A Study at the Cell Level
Plant Physiology,
May 1, 2002;
129(1):
374 - 388.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A.-C. Tang and J. S. Boyer
Growth-induced water potentials and the growth of maize leaves
J. Exp. Bot.,
March 1, 2002;
53(368):
489 - 503.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
L. van der Weerd, M. M.A.E. Claessens, T. Ruttink, F. J. Vergeldt, T. J. Schaafsma, and H. Van As
Quantitative NMR microscopy of osmotic stress responses in maize and pearl millet
J. Exp. Bot.,
December 1, 2001;
52(365):
2333 - 2343.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Munns, J. B. Passioura, J. Guo, O. Chazen, and G. R. Cramer
Water relations and leaf expansion: importance of time scale
J. Exp. Bot.,
September 1, 2000;
51(350):
1495 - 1504.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Wu and D. J. Cosgrove
Adaptation of roots to low water potentials by changes in cell wall extensibility and cell wall proteins
J. Exp. Bot.,
September 1, 2000;
51(350):
1543 - 1553.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
T. C. Hsiao and L.-K. Xu
Sensitivity of growth of roots versus leaves to water stress: biophysical analysis and relation to water transport
J. Exp. Bot.,
September 1, 2000;
51(350):
1595 - 1616.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Cavero, I. Farre, P. Debaeke, and J. M. Faci
Simulation of Maize Yield under Water Stress with the EPICphase and CROPWAT Models
Agron. J.,
July 1, 2000;
92(4):
679 - 690.
[Abstract]
[Full Text]
|
 |
|
|
|