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Leaf coordination between petiole vascular development and water demand in response to elevated CO(2) in tomato plants
The rise in atmospheric CO(2) has a profound impact on plants physiology and performance. Stomatal gas exchange such as reduction in water loss via transpiration and higher photosynthetic rates are among the key plant physiological traits altered by the increase of CO(2). Water acquired in plant roo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743362/ https://www.ncbi.nlm.nih.gov/pubmed/35028493 http://dx.doi.org/10.1002/pld3.371 |
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author | Cohen, Itay Lichston, Juliana Espada de Macêdo, Cristiane Elizabeth Costa Rachmilevitch, Shimon |
author_facet | Cohen, Itay Lichston, Juliana Espada de Macêdo, Cristiane Elizabeth Costa Rachmilevitch, Shimon |
author_sort | Cohen, Itay |
collection | PubMed |
description | The rise in atmospheric CO(2) has a profound impact on plants physiology and performance. Stomatal gas exchange such as reduction in water loss via transpiration and higher photosynthetic rates are among the key plant physiological traits altered by the increase of CO(2). Water acquired in plant roots is transported via the xylem vessels to the shoots. Under conditions of elevated CO(2), water flux decreases due to higher water use efficiency and a decline in stomatal conductance. However, the mechanism by which the shoot vascular development is affected under elevated CO(2) is still largely unclear in herbaceous crops. In the current study, tomato plants were exposed to either 400 or 800 ppm of CO(2) and were analyzed for growth, leaf area, gas exchange rate, and petiole anatomy. Elevated CO(2) caused a reduction in metaxylem vessel diameter, which in turn, decreased leaf theatrical conductivity by 400% as compared with plants grown under ambient CO(2). This work links anatomical changes in the petioles to the rise in atmospheric CO(2) and water use. Plant water demand declined under elevated CO(2), while photosynthesis increased. Thus, the decrease in leaf specific conductivity was attributed to lower water consumption in leaf gas exchange and, by extension, to higher leaf water use efficiency. As the global climate changes and water scarcity becomes more common, such anatomical alterations caused by elevated CO(2) may affect plant response to water limitation. Further research on petiole anatomical alterations under conditions of combined climate change factors such as drought and heat with elevated CO(2) may assist in clarifying the responses expected by future climate scenarios. |
format | Online Article Text |
id | pubmed-8743362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87433622022-01-12 Leaf coordination between petiole vascular development and water demand in response to elevated CO(2) in tomato plants Cohen, Itay Lichston, Juliana Espada de Macêdo, Cristiane Elizabeth Costa Rachmilevitch, Shimon Plant Direct Original Research The rise in atmospheric CO(2) has a profound impact on plants physiology and performance. Stomatal gas exchange such as reduction in water loss via transpiration and higher photosynthetic rates are among the key plant physiological traits altered by the increase of CO(2). Water acquired in plant roots is transported via the xylem vessels to the shoots. Under conditions of elevated CO(2), water flux decreases due to higher water use efficiency and a decline in stomatal conductance. However, the mechanism by which the shoot vascular development is affected under elevated CO(2) is still largely unclear in herbaceous crops. In the current study, tomato plants were exposed to either 400 or 800 ppm of CO(2) and were analyzed for growth, leaf area, gas exchange rate, and petiole anatomy. Elevated CO(2) caused a reduction in metaxylem vessel diameter, which in turn, decreased leaf theatrical conductivity by 400% as compared with plants grown under ambient CO(2). This work links anatomical changes in the petioles to the rise in atmospheric CO(2) and water use. Plant water demand declined under elevated CO(2), while photosynthesis increased. Thus, the decrease in leaf specific conductivity was attributed to lower water consumption in leaf gas exchange and, by extension, to higher leaf water use efficiency. As the global climate changes and water scarcity becomes more common, such anatomical alterations caused by elevated CO(2) may affect plant response to water limitation. Further research on petiole anatomical alterations under conditions of combined climate change factors such as drought and heat with elevated CO(2) may assist in clarifying the responses expected by future climate scenarios. John Wiley and Sons Inc. 2022-01-09 /pmc/articles/PMC8743362/ /pubmed/35028493 http://dx.doi.org/10.1002/pld3.371 Text en © 2022 The Authors. Plant Direct published by American Society of Plant Biologists and the Society for Experimental Biology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Cohen, Itay Lichston, Juliana Espada de Macêdo, Cristiane Elizabeth Costa Rachmilevitch, Shimon Leaf coordination between petiole vascular development and water demand in response to elevated CO(2) in tomato plants |
title | Leaf coordination between petiole vascular development and water demand in response to elevated CO(2) in tomato plants |
title_full | Leaf coordination between petiole vascular development and water demand in response to elevated CO(2) in tomato plants |
title_fullStr | Leaf coordination between petiole vascular development and water demand in response to elevated CO(2) in tomato plants |
title_full_unstemmed | Leaf coordination between petiole vascular development and water demand in response to elevated CO(2) in tomato plants |
title_short | Leaf coordination between petiole vascular development and water demand in response to elevated CO(2) in tomato plants |
title_sort | leaf coordination between petiole vascular development and water demand in response to elevated co(2) in tomato plants |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743362/ https://www.ncbi.nlm.nih.gov/pubmed/35028493 http://dx.doi.org/10.1002/pld3.371 |
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