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Cavitation and water fluxes driven by ice water potential in Juglans regia during freeze–thaw cycles
Freeze–thaw cycles induce major hydraulic changes due to liquid-to-ice transition within tree stems. The very low water potential at the ice–liquid interface is crucial as it may cause lysis of living cells as well as water fluxes and embolism in sap conduits, which impacts whole tree–water relation...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737071/ https://www.ncbi.nlm.nih.gov/pubmed/26585223 http://dx.doi.org/10.1093/jxb/erv486 |
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author | Charra-Vaskou, Katline Badel, Eric Charrier, Guillaume Ponomarenko, Alexandre Bonhomme, Marc Foucat, Loïc Mayr, Stefan Améglio, Thierry |
author_facet | Charra-Vaskou, Katline Badel, Eric Charrier, Guillaume Ponomarenko, Alexandre Bonhomme, Marc Foucat, Loïc Mayr, Stefan Améglio, Thierry |
author_sort | Charra-Vaskou, Katline |
collection | PubMed |
description | Freeze–thaw cycles induce major hydraulic changes due to liquid-to-ice transition within tree stems. The very low water potential at the ice–liquid interface is crucial as it may cause lysis of living cells as well as water fluxes and embolism in sap conduits, which impacts whole tree–water relations. We investigated water fluxes induced by ice formation during freeze–thaw cycles in Juglans regia L. stems using four non-invasive and complementary approaches: a microdendrometer, magnetic resonance imaging, X-ray microtomography, and ultrasonic acoustic emissions analysis. When the temperature dropped, ice nucleation occurred, probably in the cambium or pith areas, inducing high water potential gradients within the stem. The water was therefore redistributed within the stem toward the ice front. We could thus observe dehydration of the bark’s living cells leading to drastic shrinkage of this tissue, as well as high tension within wood conduits reaching the cavitation threshold in sap vessels. Ultrasonic emissions, which were strictly emitted only during freezing, indicated cavitation events (i.e. bubble formation) following ice formation in the xylem sap. However, embolism formation (i.e. bubble expansion) in stems was observed only on thawing via X-ray microtomography for the first time on the same sample. Ultrasonic emissions were detected during freezing and were not directly related to embolism formation. These results provide new insights into the complex process and dynamics of water movements and ice formation during freeze–thaw cycles in tree stems. |
format | Online Article Text |
id | pubmed-4737071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47370712016-02-03 Cavitation and water fluxes driven by ice water potential in Juglans regia during freeze–thaw cycles Charra-Vaskou, Katline Badel, Eric Charrier, Guillaume Ponomarenko, Alexandre Bonhomme, Marc Foucat, Loïc Mayr, Stefan Améglio, Thierry J Exp Bot Research Paper Freeze–thaw cycles induce major hydraulic changes due to liquid-to-ice transition within tree stems. The very low water potential at the ice–liquid interface is crucial as it may cause lysis of living cells as well as water fluxes and embolism in sap conduits, which impacts whole tree–water relations. We investigated water fluxes induced by ice formation during freeze–thaw cycles in Juglans regia L. stems using four non-invasive and complementary approaches: a microdendrometer, magnetic resonance imaging, X-ray microtomography, and ultrasonic acoustic emissions analysis. When the temperature dropped, ice nucleation occurred, probably in the cambium or pith areas, inducing high water potential gradients within the stem. The water was therefore redistributed within the stem toward the ice front. We could thus observe dehydration of the bark’s living cells leading to drastic shrinkage of this tissue, as well as high tension within wood conduits reaching the cavitation threshold in sap vessels. Ultrasonic emissions, which were strictly emitted only during freezing, indicated cavitation events (i.e. bubble formation) following ice formation in the xylem sap. However, embolism formation (i.e. bubble expansion) in stems was observed only on thawing via X-ray microtomography for the first time on the same sample. Ultrasonic emissions were detected during freezing and were not directly related to embolism formation. These results provide new insights into the complex process and dynamics of water movements and ice formation during freeze–thaw cycles in tree stems. Oxford University Press 2016-02 2015-11-19 /pmc/articles/PMC4737071/ /pubmed/26585223 http://dx.doi.org/10.1093/jxb/erv486 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Charra-Vaskou, Katline Badel, Eric Charrier, Guillaume Ponomarenko, Alexandre Bonhomme, Marc Foucat, Loïc Mayr, Stefan Améglio, Thierry Cavitation and water fluxes driven by ice water potential in Juglans regia during freeze–thaw cycles |
title | Cavitation and water fluxes driven by ice water potential in Juglans regia during freeze–thaw cycles |
title_full | Cavitation and water fluxes driven by ice water potential in Juglans regia during freeze–thaw cycles |
title_fullStr | Cavitation and water fluxes driven by ice water potential in Juglans regia during freeze–thaw cycles |
title_full_unstemmed | Cavitation and water fluxes driven by ice water potential in Juglans regia during freeze–thaw cycles |
title_short | Cavitation and water fluxes driven by ice water potential in Juglans regia during freeze–thaw cycles |
title_sort | cavitation and water fluxes driven by ice water potential in juglans regia during freeze–thaw cycles |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737071/ https://www.ncbi.nlm.nih.gov/pubmed/26585223 http://dx.doi.org/10.1093/jxb/erv486 |
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