|
PLANT PHYSIOLOGY , Vol 107, Issue 2 377-384, Copyright © 1995 by American Society of Plant Biologists
|
WHOLE PLANT, ENVIRONMENTAL, AND STRESS PHYSIOLOGY |
Export of Abscisic Acid, 1-Aminocyclopropane-1-Carboxylic Acid, Phosphate, and Nitrate from Roots to Shoots of Flooded Tomato Plants (Accounting for Effects of Xylem Sap Flow Rate on Concentration and Delivery)
M. A. Else, K. C. Hall, G. M. Arnold, W. J. Davies and M. B. Jackson
Department of Agricultural Sciences, University of Bristol, Institute of Arable Crops Research, Long Ashton Research Station, Bristol BS18 9AF, United Kingdom (M.A.E., K.C.H., G.M.A., M.B.J.)
We determined whether root stress alters the output of physiologically
active messages passing from roots to shoots in the transpiration stream.
Concentrations were not good measures of output. This was because changes
in volume flow of xylem sap caused either by sampling procedures or by
effects of root stress on rates of whole-plant transpiration modified
concentrations simply by dilution. Thus, delivery rate (concentration x sap
flow rate) was preferred to concentration as a measure of solute output
from roots. To demonstrate these points, 1-aminocyclopropane-1-carboxylic
acid (ACC), abscisic acid, phosphate, nitrate, and pH were measured in
xylem sap of flooded and well-drained tomato (Lycopersicon esculentum
Mill., cv Ailsa Craig) plants expressed at various rates from pressurized
detopped roots. Concentrations decreased as sap flow rates were increased.
However, dilution of solutes was often less than proportional to flow,
especially in flooded plants. Thus, sap flowing through detopped roots at
whole-plant transpiration rates was used to estimate solute delivery rates
in intact plants. On this basis, delivery of ACC from roots to shoots was
3.1-fold greater in plants flooded for 24 h than in well-drained plants,
and delivery of phosphate was 2.3-fold greater. Delivery rates of abscisic
acid and nitrate in flooded plants were only 11 and 7%, respectively, of
those in well-drained plants.
This article has been cited by other articles:

|
 |

|
 |
 
S. K. Field, J. P. Smith, B. P. Holzapfel, W. J. Hardie, and R.J. N. Emery
Grapevine Response to Soil Temperature: Xylem Cytokinins and Carbohydrate Reserve Mobilization from Budbreak to Anthesis
Am. J. Enol. Vitic.,
June 1, 2009;
60(2):
164 - 172.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
I. C. Dodd, G. Egea, and W. J. Davies
Accounting for sap flow from different parts of the root system improves the prediction of xylem ABA concentration in plants grown with heterogeneous soil moisture
J. Exp. Bot.,
November 1, 2008;
59(15):
4083 - 4093.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. M. Neumann
Evidence for long-distance xylem transport of signal peptide activity from tomato roots
J. Exp. Bot.,
June 1, 2007;
58(8):
2217 - 2223.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. A. Else, J. M. Taylor, and C. J. Atkinson
Anti-transpirant activity in xylem sap from flooded tomato (Lycopersicon esculentum Mill.) plants is not due to pH-mediated redistributions of root- or shoot-sourced ABA
J. Exp. Bot.,
September 1, 2006;
57(12):
3349 - 3357.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
I. C. Dodd and C. A. Beveridge
Xylem-borne cytokinins: still in search of a role?
J. Exp. Bot.,
January 1, 2006;
57(1):
1 - 4.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Q. D. Goodger, R. E. Sharp, E. L. Marsh, and D. P. Schachtman
Relationships between xylem sap constituents and leaf conductance of well-watered and water-stressed maize across three xylem sap sampling techniques
J. Exp. Bot.,
September 1, 2005;
56(419):
2389 - 2400.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Oda, C. Sakuta, S. Masuda, T. Mizoguchi, H. Kamada, and S. Satoh
Possible Involvement of Leaf Gibberellins in the Clock-Controlled Expression of XSP30, a Gene Encoding a Xylem Sap Lectin, in Cucumber Roots
Plant Physiology,
December 1, 2003;
133(4):
1779 - 1790.
[Abstract]
[Full Text]
|
 |
|

|
 |

|
 |
 
I. C. Dodd, L. P. Tan, and J. He
Do increases in xylem sap pH and/or ABA concentration mediate stomatal closure following nitrate deprivation?
J. Exp. Bot.,
April 1, 2003;
54(385):
1281 - 1288.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. B. Jackson
Long-distance signalling from roots to shoots assessed: the flooding story
J. Exp. Bot.,
February 1, 2002;
53(367):
175 - 181.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Borel and T. Simonneau
Is the ABA concentration in the sap collected by pressurizing leaves relevant for analysing drought effects on stomata? Evidence from ABA-fed leaves of transgenic plants with modified capacities to synthesize ABA
J. Exp. Bot.,
February 1, 2002;
53(367):
287 - 296.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
W. Hartung, A. Sauter, and E. Hose
Abscisic acid in the xylem: where does it come from, where does it go to?
J. Exp. Bot.,
January 1, 2002;
53(366):
27 - 32.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Hose, D.T. Clarkson, E. Steudle, L. Schreiber, and W. Hartung
The exodermis: a variable apoplastic barrier
J. Exp. Bot.,
December 1, 2001;
52(365):
2245 - 2264.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. Vernieri, A. Lenzi, M. Figaro, F. Tognoni, and A. Pardossi
How the roots contribute to the ability of Phaseolus vulgaris L. to cope with chilling-induced water stress
J. Exp. Bot.,
November 1, 2001;
52(364):
2199 - 2206.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Sauter, W.J. Davies, and W. Hartung
The long-distance abscisic acid signal in the droughted plant: the fate of the hormone on its way from root to shoot
J. Exp. Bot.,
October 1, 2001;
52(363):
1991 - 1997.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. W.H. Yong, S. C. Wong, D. S. Letham, C. H. Hocart, and G. D. Farquhar
Effects of Elevated [CO2] and Nitrogen Nutrition on Cytokinins in the Xylem Sap and Leaves of Cotton
Plant Physiology,
October 1, 2000;
124(2):
767 - 780.
[Abstract]
[Full Text]
|
 |
|

|
 |

|
 |
 
W. J. Davies, M. A. Bacon, D. Stuart Thompson, W. Sobeih, and L. Gonzalez Rodriguez
Regulation of leaf and fruit growth in plants growing in drying soil: exploitation of the plants' chemical signalling system and hydraulic architecture to increase the efficiency of water use in agriculture
J. Exp. Bot.,
September 1, 2000;
51(350):
1617 - 1626.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A.G. Netting
pH, abscisic acid and the integration of metabolism in plants under stressed and non-stressed conditions: cellular responses to stress and their implication for plant water relations
J. Exp. Bot.,
February 2, 2000;
51(343):
147 - 158.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. Walch-Liu, G. Neumann, F. Bangerth, and C. Engels
Rapid effects of nitrogen form on leaf morphogenesis in tobacco
J. Exp. Bot.,
February 2, 2000;
51(343):
227 - 237.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H.-J. Chung and R. J. Ferl
Arabidopsis Alcohol Dehydrogenase Expression in Both Shoots and Roots Is Conditioned by Root Growth Environment
Plant Physiology,
October 1, 1999;
121(2):
429 - 436.
[Abstract]
[Full Text]
|
 |
|

|
 |

|
 |
 
M. Kamaluddin and J. J. Zwiazek
Ethylene Enhances Water Transport in Hypoxic Aspen
Plant Physiology,
March 1, 2002;
128(3):
962 - 969.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|