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Daytime depression in temperature-normalised stem CO2 efflux in young poplar trees is dominated by low turgor pressure rather than by internal transport of respired CO2.

Identifieur interne : 000F72 ( Main/Exploration ); précédent : 000F71; suivant : 000F73

Daytime depression in temperature-normalised stem CO2 efflux in young poplar trees is dominated by low turgor pressure rather than by internal transport of respired CO2.

Auteurs : Roberto L. Salom N [Belgique, Espagne] ; Veerle De Schepper [Belgique] ; María Valbuena-Caraba A [Espagne] ; Luis Gil [Espagne] ; Kathy Steppe [Belgique]

Source :

RBID : pubmed:28984360

Descripteurs français

English descriptors

Abstract

Daytime decreases in temperature-normalised stem CO2 efflux (EA_D ) are commonly ascribed to internal transport of respired CO2 (FT ) or to an attenuated respiratory activity due to lowered turgor pressure. The two are difficult to separate as they are simultaneously driven by sap flow dynamics. To achieve combined gradients in turgor pressure and FT , sap flow rates in poplar trees were manipulated through severe defoliation, severe drought, moderate defoliation and moderate drought. Turgor pressure was mechanistically modelled using measurements of sap flow, stem diameter variation, and soil and stem water potential. A mass balance approach considering internal and external CO2 fluxes was applied to estimate FT . Under well-watered control conditions, both turgor pressure and sap flow, as a proxy of FT , were reliable predictors of EA_D . After tree manipulation, only turgor pressure was a robust predictor of EA_D . Moreover, FT accounted for < 15% of EA_D . Our results suggest that daytime reductions in turgor pressure and associated constrained growth are the main cause of EA_D in young poplar trees. Turgor pressure is determined by both carbohydrate supply and water availability, and should be considered to improve our widely used but inaccurate temperature-based predictions of woody tissue respiration in global models.

DOI: 10.1111/nph.14831
PubMed: 28984360


Affiliations:


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Le document en format XML

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<term>Biological Transport (MeSH)</term>
<term>Carbon Dioxide (metabolism)</term>
<term>Cell Respiration (MeSH)</term>
<term>Linear Models (MeSH)</term>
<term>Plant Stems (metabolism)</term>
<term>Populus (physiology)</term>
<term>Pressure (MeSH)</term>
<term>Temperature (MeSH)</term>
<term>Time Factors (MeSH)</term>
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<term>Arbres (physiologie)</term>
<term>Dioxyde de carbone (métabolisme)</term>
<term>Eau (MeSH)</term>
<term>Facteurs temps (MeSH)</term>
<term>Modèles linéaires (MeSH)</term>
<term>Populus (physiologie)</term>
<term>Pression (MeSH)</term>
<term>Respiration cellulaire (MeSH)</term>
<term>Température (MeSH)</term>
<term>Tiges de plante (métabolisme)</term>
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<term>Plant Stems</term>
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<term>Dioxyde de carbone</term>
<term>Tiges de plante</term>
<term>Xylème</term>
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<term>Arbres</term>
<term>Populus</term>
</keywords>
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<term>Populus</term>
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<div type="abstract" xml:lang="en">Daytime decreases in temperature-normalised stem CO
<sub>2</sub>
efflux (E
<sub>A</sub>
<sub>_D</sub>
) are commonly ascribed to internal transport of respired CO
<sub>2</sub>
(F
<sub>T</sub>
) or to an attenuated respiratory activity due to lowered turgor pressure. The two are difficult to separate as they are simultaneously driven by sap flow dynamics. To achieve combined gradients in turgor pressure and F
<sub>T</sub>
, sap flow rates in poplar trees were manipulated through severe defoliation, severe drought, moderate defoliation and moderate drought. Turgor pressure was mechanistically modelled using measurements of sap flow, stem diameter variation, and soil and stem water potential. A mass balance approach considering internal and external CO
<sub>2</sub>
fluxes was applied to estimate F
<sub>T</sub>
. Under well-watered control conditions, both turgor pressure and sap flow, as a proxy of F
<sub>T</sub>
, were reliable predictors of E
<sub>A</sub>
<sub>_D</sub>
. After tree manipulation, only turgor pressure was a robust predictor of E
<sub>A</sub>
<sub>_D</sub>
. Moreover, F
<sub>T</sub>
accounted for < 15% of E
<sub>A</sub>
<sub>_D</sub>
. Our results suggest that daytime reductions in turgor pressure and associated constrained growth are the main cause of E
<sub>A</sub>
<sub>_D</sub>
in young poplar trees. Turgor pressure is determined by both carbohydrate supply and water availability, and should be considered to improve our widely used but inaccurate temperature-based predictions of woody tissue respiration in global models.</div>
</front>
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<sub>2</sub>
efflux in young poplar trees is dominated by low turgor pressure rather than by internal transport of respired CO
<sub>2</sub>
.</ArticleTitle>
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<AbstractText>Daytime decreases in temperature-normalised stem CO
<sub>2</sub>
efflux (E
<sub>A</sub>
<sub>_D</sub>
) are commonly ascribed to internal transport of respired CO
<sub>2</sub>
(F
<sub>T</sub>
) or to an attenuated respiratory activity due to lowered turgor pressure. The two are difficult to separate as they are simultaneously driven by sap flow dynamics. To achieve combined gradients in turgor pressure and F
<sub>T</sub>
, sap flow rates in poplar trees were manipulated through severe defoliation, severe drought, moderate defoliation and moderate drought. Turgor pressure was mechanistically modelled using measurements of sap flow, stem diameter variation, and soil and stem water potential. A mass balance approach considering internal and external CO
<sub>2</sub>
fluxes was applied to estimate F
<sub>T</sub>
. Under well-watered control conditions, both turgor pressure and sap flow, as a proxy of F
<sub>T</sub>
, were reliable predictors of E
<sub>A</sub>
<sub>_D</sub>
. After tree manipulation, only turgor pressure was a robust predictor of E
<sub>A</sub>
<sub>_D</sub>
. Moreover, F
<sub>T</sub>
accounted for < 15% of E
<sub>A</sub>
<sub>_D</sub>
. Our results suggest that daytime reductions in turgor pressure and associated constrained growth are the main cause of E
<sub>A</sub>
<sub>_D</sub>
in young poplar trees. Turgor pressure is determined by both carbohydrate supply and water availability, and should be considered to improve our widely used but inaccurate temperature-based predictions of woody tissue respiration in global models.</AbstractText>
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<DescriptorName UI="D002245" MajorTopicYN="N">Carbon Dioxide</DescriptorName>
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</MeshHeading>
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<DescriptorName UI="D016014" MajorTopicYN="N">Linear Models</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018547" MajorTopicYN="N">Plant Stems</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading>
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<MeshHeading>
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<MeshHeading>
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<Keyword MajorTopicYN="Y">Populus × Canadensis Moench ‘Vesten’</Keyword>
<Keyword MajorTopicYN="Y">carbon fluxes</Keyword>
<Keyword MajorTopicYN="Y">growth respiration</Keyword>
<Keyword MajorTopicYN="Y">maintenance respiration</Keyword>
<Keyword MajorTopicYN="Y">mechanistic modelling</Keyword>
<Keyword MajorTopicYN="Y">radial stem growth</Keyword>
<Keyword MajorTopicYN="Y">transpiration</Keyword>
<Keyword MajorTopicYN="Y">xylem CO2 transport</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="received">
<Year>2017</Year>
<Month>06</Month>
<Day>14</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2017</Year>
<Month>09</Month>
<Day>01</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2017</Year>
<Month>10</Month>
<Day>7</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2019</Year>
<Month>9</Month>
<Day>13</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2017</Year>
<Month>10</Month>
<Day>7</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">28984360</ArticleId>
<ArticleId IdType="doi">10.1111/nph.14831</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>Belgique</li>
<li>Espagne</li>
</country>
<region>
<li>Communauté de Madrid</li>
<li>Province de Flandre-Orientale</li>
<li>Région flamande</li>
</region>
<settlement>
<li>Gand</li>
<li>Madrid</li>
</settlement>
<orgName>
<li>Université de Gand</li>
</orgName>
</list>
<tree>
<country name="Belgique">
<region name="Région flamande">
<name sortKey="Salom N, Roberto L" sort="Salom N, Roberto L" uniqKey="Salom N R" first="Roberto L" last="Salom N">Roberto L. Salom N</name>
</region>
<name sortKey="De Schepper, Veerle" sort="De Schepper, Veerle" uniqKey="De Schepper V" first="Veerle" last="De Schepper">Veerle De Schepper</name>
<name sortKey="Steppe, Kathy" sort="Steppe, Kathy" uniqKey="Steppe K" first="Kathy" last="Steppe">Kathy Steppe</name>
</country>
<country name="Espagne">
<region name="Communauté de Madrid">
<name sortKey="Salom N, Roberto L" sort="Salom N, Roberto L" uniqKey="Salom N R" first="Roberto L" last="Salom N">Roberto L. Salom N</name>
</region>
<name sortKey="Gil, Luis" sort="Gil, Luis" uniqKey="Gil L" first="Luis" last="Gil">Luis Gil</name>
<name sortKey="Valbuena Caraba A, Maria" sort="Valbuena Caraba A, Maria" uniqKey="Valbuena Caraba A M" first="María" last="Valbuena-Caraba A">María Valbuena-Caraba A</name>
</country>
</tree>
</affiliations>
</record>

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