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Assimilation of xylem-transported (13)C-labelled CO(2) in leaves and branches of sycamore (Platanus occidentalis L.)

Previous reports have shown that CO(2) dissolved in xylem sap in tree stems can move upward in the transpiration stream. To determine the fate of this dissolved CO(2), the internal transport of respired CO(2) at high concentration from the bole of the tree was simulated by allowing detached young br...

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Autores principales: McGuire, M. A., Marshall, J. D., Teskey, R. O.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2736895/
https://www.ncbi.nlm.nih.gov/pubmed/19602545
http://dx.doi.org/10.1093/jxb/erp222
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author McGuire, M. A.
Marshall, J. D.
Teskey, R. O.
author_facet McGuire, M. A.
Marshall, J. D.
Teskey, R. O.
author_sort McGuire, M. A.
collection PubMed
description Previous reports have shown that CO(2) dissolved in xylem sap in tree stems can move upward in the transpiration stream. To determine the fate of this dissolved CO(2), the internal transport of respired CO(2) at high concentration from the bole of the tree was simulated by allowing detached young branches of sycamore (Platanus occidentalis L.) to transpire water enriched with a known quantity of (13)CO(2) in sunlight. Simultaneously, leaf net photosynthesis and CO(2) efflux from woody tissue were measured. Branch and leaf tissues were subsequently analysed for (13)C content to determine the quantity of transported (13)CO(2) label that was fixed. Treatment branches assimilated an average of 35% (SE=2.4) of the (13)CO(2) label taken up in the treatment water. The majority was fixed in the woody tissue of the branches, with smaller amounts fixed in the leaves and petioles. Overall, the fixation of internally transported (13)CO(2) label by woody tissues averaged 6% of the assimilation of CO(2) from the atmosphere by the leaves. Woody tissue assimilation rates calculated from measurements of (13)C differed from rates calculated from measurements of CO(2) efflux in the lower branch but not in the upper branch. The results of this study showed unequivocally that CO(2) transported in xylem sap can be fixed in photosynthetic cells in the leaves and branches of sycamore trees and provided evidence that recycling of xylem-transported CO(2) may be an important means by which trees reduce the carbon cost of respiration.
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spelling pubmed-27368952009-09-03 Assimilation of xylem-transported (13)C-labelled CO(2) in leaves and branches of sycamore (Platanus occidentalis L.) McGuire, M. A. Marshall, J. D. Teskey, R. O. J Exp Bot Research Papers Previous reports have shown that CO(2) dissolved in xylem sap in tree stems can move upward in the transpiration stream. To determine the fate of this dissolved CO(2), the internal transport of respired CO(2) at high concentration from the bole of the tree was simulated by allowing detached young branches of sycamore (Platanus occidentalis L.) to transpire water enriched with a known quantity of (13)CO(2) in sunlight. Simultaneously, leaf net photosynthesis and CO(2) efflux from woody tissue were measured. Branch and leaf tissues were subsequently analysed for (13)C content to determine the quantity of transported (13)CO(2) label that was fixed. Treatment branches assimilated an average of 35% (SE=2.4) of the (13)CO(2) label taken up in the treatment water. The majority was fixed in the woody tissue of the branches, with smaller amounts fixed in the leaves and petioles. Overall, the fixation of internally transported (13)CO(2) label by woody tissues averaged 6% of the assimilation of CO(2) from the atmosphere by the leaves. Woody tissue assimilation rates calculated from measurements of (13)C differed from rates calculated from measurements of CO(2) efflux in the lower branch but not in the upper branch. The results of this study showed unequivocally that CO(2) transported in xylem sap can be fixed in photosynthetic cells in the leaves and branches of sycamore trees and provided evidence that recycling of xylem-transported CO(2) may be an important means by which trees reduce the carbon cost of respiration. Oxford University Press 2009-09 2009-07-14 /pmc/articles/PMC2736895/ /pubmed/19602545 http://dx.doi.org/10.1093/jxb/erp222 Text en © 2009 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details)
spellingShingle Research Papers
McGuire, M. A.
Marshall, J. D.
Teskey, R. O.
Assimilation of xylem-transported (13)C-labelled CO(2) in leaves and branches of sycamore (Platanus occidentalis L.)
title Assimilation of xylem-transported (13)C-labelled CO(2) in leaves and branches of sycamore (Platanus occidentalis L.)
title_full Assimilation of xylem-transported (13)C-labelled CO(2) in leaves and branches of sycamore (Platanus occidentalis L.)
title_fullStr Assimilation of xylem-transported (13)C-labelled CO(2) in leaves and branches of sycamore (Platanus occidentalis L.)
title_full_unstemmed Assimilation of xylem-transported (13)C-labelled CO(2) in leaves and branches of sycamore (Platanus occidentalis L.)
title_short Assimilation of xylem-transported (13)C-labelled CO(2) in leaves and branches of sycamore (Platanus occidentalis L.)
title_sort assimilation of xylem-transported (13)c-labelled co(2) in leaves and branches of sycamore (platanus occidentalis l.)
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2736895/
https://www.ncbi.nlm.nih.gov/pubmed/19602545
http://dx.doi.org/10.1093/jxb/erp222
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