Plant Physiology 92:1053-1061 (1990)
© 1990 American Society of Plant Biologists
Environmental and Stress Physiology
Light Energy Dissipation under Water Stress Conditions
Contribution of Reassimilation and Evidence for Additional Processes
Thomas Stuhlfauth,
Ralph Scheuermann and
Heinrich P. Fock
Fachbereich Biologie, Universität Kaiserslautern, Postfach 3049, D-6750 Kaiserslautern, Federal Republic of Germany
Using 14CO2 gas exchange and metabolite analyses, stomatal as well as total internal CO2 uptake and evolution were estimated. Pulse modulated fluorescence was measured during induction and steady state of photosynthesis. Leaf water potential of Digitalis lanata EHRH. plants decreased to 2.5 megapascals after withholding irrigation. By osmotic adjustment, leaves remained turgid and fully exposed to irradiance even at severe water stress. Due to the stress-induced reduction of stomatal conductance, the stomatal CO2 exchange was drastically reduced, whereas the total CO2 uptake and evolution were less affected. Stomatal closure induced an increase in the reassimilation of internally evolved CO2. This `CO2 recycling' consumes a significant amount of light energy in the form of ATP and reducing equivalents. As a consequence, the metabolic demand for light energy is only reduced by about 40%, whereas net photosynthesis is diminished by about 70% under severe stress conditions. By CO2 recycling, carbon flux, enzymatic substrate turnover and consumption of light energy were maintained at high levels, which enabled the plant to recover rapidly after rewatering. In stressed D. lanata plants a variable fluorescence quenching mechanism, termed `coefficient of actinic light quenching,' was observed. Besides water conservation, light energy dissipation is essential and involves regulated metabolic variations.
This article has been cited by other articles:

|
 |

|
 |
 
S. Koussevitzky, N. Suzuki, S. Huntington, L. Armijo, W. Sha, D. Cortes, V. Shulaev, and R. Mittler
Ascorbate Peroxidase 1 Plays a Key Role in the Response of Arabidopsis thaliana to Stress Combination
J. Biol. Chem.,
December 5, 2008;
283(49):
34197 - 34203.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. HAUPT-HERTING and H. P. FOCK
Oxygen Exchange in Relation to Carbon Assimilation in Water-stressed Leaves During Photosynthesis
Ann. Bot.,
June 15, 2002;
89(7):
851 - 859.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. FLEXAS and H. MEDRANO
Drought-inhibition of Photosynthesis in C3 Plants: Stomatal and Non-stomatal Limitations Revisited
Ann. Bot.,
February 1, 2002;
89(2):
183 - 189.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Haupt-Herting, K. Klug, and H. P. Fock
A New Approach to Measure Gross CO2 Fluxes in Leaves. Gross CO2 Assimilation, Photorespiration, and Mitochondrial Respiration in the Light in Tomato under Drought Stress
Plant Physiology,
May 1, 2001;
126(1):
388 - 396.
[Abstract]
[Full Text]
|
 |
|

|
 |

|
 |
 
J. Flexas, M. Badger, W. S. Chow, H. Medrano, and C. B. Osmond
Analysis of the Relative Increase in Photosynthetic O2 Uptake When Photosynthesis in Grapevine Leaves Is Inhibited following Low Night Temperatures and/or Water Stress
Plant Physiology,
October 1, 1999;
121(2):
675 - 684.
[Abstract]
[Full Text]
|
 |
|
|
|