Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
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 ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (23)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Peuke, A. D.
Right arrow Articles by Hartung, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Peuke, A. D.
Right arrow Articles by Hartung, W.
Agricola
Right arrow Articles by Peuke, A. D.
Right arrow Articles by Hartung, W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Experimental Botany, Vol. 53, No. 367, pp. 241-250, February 1, 2002
© 2002 Oxford University Press


Original Papers

Flows of elements, ions and abscisic acid in Ricinus communis and site of nitrate reduction under potassium limitation

Andreas D. Peuke1, W. Dieter Jeschke and Wolfram Hartung

Julius-von-Sachs-Institut für Biowissenschaften der Universität Würzburg, Lehrstuhl Botanik I der Universität, Julius-von-Sachs-Platz 2, D-97082 Würzburg, Germany

In a pot experiment Ricinus communis plants were cultivated in quartz sand and supplied daily with a nutrient solution which contained 4 mol m-3 nitrate as the nitrogen source and either full strength potassium (1.3 mol m-3, control) or 8% potassium (0.1 mol m-3, K+-limitation). Although the final fresh weight of the whole plant was not affected by K+-limitation, the root–shoot ratio was increased due to a relatively increased root growth and inhibited development of younger shoot parts. Owing to K+-limitation, photosynthesis was slightly decreased, while dark respiration of the shoot markedly decreased and root respiration was nearly doubled. The transport of carbon in the phloem, and to some extent in the xylem, was greater and the root was favoured in the partitioning of carbon. This was also true for nitrogen and potassium which were both taken up at lower rates, particularly potassium. In these two cases a high remobilization and recycling from the old part of the shoot was observed. By contrast, uptake of sodium was 2.4-fold higher under K+-limitation and this resulted in increased flows in the plants, which was discussed generally as a means for charge balance (in combination with a slight increase in uptake of magnesium and calcium). Nitrate reduction took place in the same portion in the root and shoot. This was a shift to the root compared to the control and points to an inhibition of xylem transport caused by limitation of K+ as an easily permeating countercation. Low K+ supply also resulted in an increased biosynthesis of ABA in the roots (265%). This caused a slightly increased deposition of ABA in the roots (193%) and a 4.6-fold higher root-to-shoot and a doubled shoot-to-root ABA signal in the xylem or phloem, respectively. The high degradation of ABA in the shoots prevented ABA accumulation there.

Key words: Ricinus communis L., potassium limitation, cations, anions, ABA, phloem transport, xylem transport.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Plant Physiol.Home page
M. J. Kim, R. Shin, and D. P. Schachtman
A Nuclear Factor Regulates Abscisic Acid Responses in Arabidopsis
Plant Physiology, November 1, 2009; 151(3): 1433 - 1445.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
R. Aroca, P. Vernieri, and J. M. Ruiz-Lozano
Mycorrhizal and non-mycorrhizal Lactuca sativa plants exhibit contrasting responses to exogenous ABA during drought stress and recovery
J. Exp. Bot., May 9, 2008; (2008) ern057v1.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
F. Jiang, W. D. Jeschke, W. Hartung, and D. D. Cameron
Does legume nitrogen fixation underpin host quality for the hemiparasitic plant Rhinanthus minor?
J. Exp. Bot., March 1, 2008; 59(4): 917 - 925.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
F. Jiang and W. Hartung
Long-distance signalling of abscisic acid (ABA): the factors regulating the intensity of the ABA signal
J. Exp. Bot., January 1, 2008; 59(1): 37 - 43.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
S. Kanai, K. Ohkura, J. J. Adu-Gyamfi, P. K. Mohapatra, N. T. Nguyen, H. Saneoka, and K. Fujita
Depression of sink activity precedes the inhibition of biomass production in tomato plants subjected to potassium deficiency stress
J. Exp. Bot., August 1, 2007; 58(11): 2917 - 2928.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
D. Schraut, H. Heilmeier, and W. Hartung
Radial transport of water and abscisic acid (ABA) in roots of Zea mays under conditions of nutrient deficiency
J. Exp. Bot., March 1, 2005; 56(413): 879 - 886.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.