Plant Physiol. Journal of Pharmacology and Experimental Therapeutics
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Plant Physiology 65:1111-1115 (1980)
© 1980 American Society of Plant Biologists

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Web of Science (78)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Setter, T. L.
Right arrow Articles by Brenner, M. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Setter, T. L.
Right arrow Articles by Brenner, M. L.
Agricola
Right arrow Articles by Setter, T. L.
Right arrow Articles by Brenner, M. L.
Articles

Effect of Obstructed Translocation on Leaf Abscisic Acid, and Associated Stomatal Closure and Photosynthesis Decline 1

Tim L. Setter, William A. Brun2 and Mark L. Brenner

Department of Agronomy and Plant Genetics, University of Minnesota, St. Paul, Minnesota, 2 Department of Horticultural Science and Landscape Architecture, University of Minnesota, St. Paul, Minnesota

Pod removal or petiole girdling, which causes obstruction of translocation, was found in our previous study to cause reduced rates of photosynthesis in soybean leaves due to stomatal closure. The purpose of this research was to determine the involvement of photoassimilate accumulation and leaf abscisic acid (ABA) levels in the mechanism of stomatal closure induced by such treatments.

Leaf glucose and sucrose levels increased during the initial 12-hour period after depodding or petiole girdling. Starch, which represents a much larger pool of leaf carbohydrate, was not perceptibly increased above control levels during the 12-hour posttreatment period.

When leaflets were exposed to nonphotosynthetic environments (shading or CO2-free air) for a 24-hour period after the translocation-obstructing treatments were applied and then returned to normal light or CO2 concentration, stomatal diffusive conductivity was reduced 65% and 85% with depodding and girdling, respectively. These reductions were comparable to those previously observed without an intervening nonphotosynthetic exposure, thus indicating that photosynthate accumulations were not necessary for the observed response.

Free and bound ABA (released on alkaline hydrolysis) were determined by gas liquid chromatography with electron capture detection following preparative high performance liquid chromatography. Free ABA in monitored leaves increased almost 10-fold 48 hours after complete depodding and 25-fold 24 hours after petiole girdling of such leaves. By 3 hours after treatment, in a time course study, free ABA had increased 2-fold above control values in depodded and 5-fold in girdled leaves. Leaf concentrations of bound ABA did not appear to be related to the treatment effects on stomata.

Thus, the translocation-obstructing treatments cause an increased level of ABA by a mechanism not involving accumulation of photoassimilate. Increased leaf ABA levels, which were independent of water stress or leaf water potential, appear to be involved in the stomatal closure response. It is suggested that the mechanism of increased leaf ABA levels following translocation-obstruction may be due to an interference with normal translocation of ABA out of leaves.


1 Contribution from the Agricultural Experimental Station, University of Minnesota, St. Paul, Minnesota 55108. Paper No. 11,035, Scientific Journal Series. This research was supported in part by the Science and Education Administration of the United States Department of Agriculture under Grant 5901-0410-8-0183-0 from the Competitive Research Grants Office. This research was also supported in part by a Grant from the Minnesota Soybean Research and Promotion Council and in part by CSRS Grant 701-15-28.




This article has been cited by other articles:


Home page
jashsHome page
D. G. Mortley, C. K. Bonsi, W. A. Hill, C. E. Morris, C. S. Williams, C. F. Davis, J. W. Williams, L. H. Levine, B. V. Petersen, and R. M. Wheeler
Influence of Microgravity Environment on Root Growth, Soluble Sugars, and Starch Concentration of Sweetpotato Stem Cuttings
J. Amer. Soc. Hort. Sci., May 1, 2008; 133(3): 327 - 332.
[Abstract] [Full Text] [PDF]


Home page
Agron. J.Home page
J. Yang, J. Zhang, Z. Wang, Q. Zhu, and L. Liu
Water Deficit-Induced Senescence and Its Relationship to the Remobilization of Pre-Stored Carbon in Wheat during Grain Filling
Agron. J., January 1, 2001; 93(1): 196 - 206.
[Abstract] [Full Text]


Home page
Crop Sci.Home page
W.P. Bruening and D.B. Egli
Relationship between Photosynthesis and Seed Number at Phloem Isolated Nodes in Soybean
Crop Sci., November 1, 1999; 39(6): 1769 - 1775.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1980 by the American Society of Plant Biologists