Leaf shrinkage decreases porosity at low water potentials in sunflower
An-Ching Tang A and John S. Boyer A BA College of Marine Studies and College of Agriculture and Natural Resources, University of Delaware, Lewes, DE 19958, USA.
B Corresponding author. Email: boyer@cms.udel.edu
Functional Plant Biology 34(1) 24-30 https://doi.org/10.1071/FP06222
Submitted: 7 September 2006 Accepted: 23 November 2006 Published: 19 January 2007
Abstract
Leaves often shrink significantly when soil water is limited. For gas exchange measurmements, the shrinkage can require correction for changing amounts of tissue in the apparatus. In sunflower plants (Helianthus annuus L.), a comparison was made between mathematically-corrected transpiration and clamping leaves at their original turgid size without mathematical correction. These methods should give the same result, but transpiration was substantially greater in the clamped leaves than in the shrunken and mathematically-corrected ones. Because the clamped leaves remained at their original turgid area, wounding was not a factor. If shrunken leaves were stretched to their original area, transpiration increased immediately and was traced to increased leaf conductance to water vapor and greater porosity for bulk air movement through the leaf, implicating the stomata. Releasing the leaf caused each of these properties to return to the tightened condition. When all the leaves were held at their original size during a soil water deficit, whole-plant water use was greater than when the leaves shrank naturally. It was concluded that shrinkage decreases the porosity of sunflower leaves. This natural tightening can be disrupted by stretching leaves during gas exchange measurements. However, stretching provides a useful means of changing leaf porosity for experimental purposes.
Additional keywords: conductance to water vapor, dehydration, gas exchange, Helianthus annuus, transpiration, water potential.
Acknowledgements
We thank Interstate Payco Seed Co. for a generous gift of sunflower seeds.
Boyer JS
(1971) Recovery of photosynthesis in sunflower after a period of low leaf water potential. Plant Physiology 47, 816–820.
| PubMed |
Boyer JS, Bowen BL
(1970) Inhibition of oxygen evolution in chloroplasts isolated from leaves with low water potentials. Plant Physiology 45, 612–615.
| PubMed |
Boyer JS, Knipling EB
(1965) Isopiestic technique for measuring water potentials in leaves with a thermocouple psychrometer. Proceedings of the National Academy of Sciences USA 54, 1044–1051.
| Crossref | GoogleScholarGoogle Scholar |
Boyer JS, Potter JR
(1973) Chloroplast response to low leaf water potentials. I. Role of turgor. Plant Physiology 51, 989–992.
| PubMed |
Ehret DL, Boyer JS
(1979) Potassium loss from stomatal guard cells at low water potentials. Journal of Experimental Botany 30, 225–234.
| Crossref |
Fambrini M,
Pugliesi C,
Vernieri P,
Pardossi A, Baroncelli S
(1994) Characterization of a wilty sunflower (Helianthus annuus L.) mutant. II. Water relations, stomatal conductance, abscisic acid content in leaves and xylem sap of plants subjected to water deficiency. Journal of Experimental Botany 45, 1809–1815.
| Crossref |
Fellows RJ, Boyer JS
(1978) Altered ultrastructure of cells of sunflower leaves having low water potentials. Protoplasma 93, 381–395.
| Crossref |
Hoagland DR, Arnon DI
(1950) The water culture method for growing plants without soil. California Agricultural Experiment Station Circular 347, 1–32.
Jones MM, Turner NC
(1980) Osmotic adjustment in expanding and fully expanded leaves of sunflower in response to water deficits. Australian Journal of Plant Physiology 7, 181–192.
Kawamitsu Y,
Driscoll T, Boyer JS
(2000) Photosynthesis during desiccation in an intertidal alga and a land plant. Plant and Cell Physiology 41, 344–353.
| PubMed |
Matthews MA, Boyer JS
(1984) Acclimation of photosynthesis to low water potentials. Plant Physiology 74, 161–166.
| PubMed |
Peña-Rojas K,
Aranda X,
Joffre R, Fleck I
(2005) Leaf morphology, photochemistry and water status changes in resprouting Quercus ilex during drought. Functional Plant Biology 32, 117–130.
| Crossref | GoogleScholarGoogle Scholar |
Turner NC,
Schulze E-D, Gollan T
(1985) The responses of stomata and leaf gas exchange to vapour pressure deficits and soil water content. II. In the mesophytic herbaceous species Helianthus annuus. Oecologia 65, 348–355.
| Crossref | GoogleScholarGoogle Scholar |