In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carbon

Detalhes bibliográficos
Autor(a) principal: Epron, Daniel
Data de Publicação: 2015
Outros Autores: Cabral, Osvaldo Machado Rodrigues, Laclau, Jean-Paul [UNESP], Dannoura, Masako, Packer, Ana Paula, Plain, Caroline, Battie-Laclau, Patricia, Moreira, Marcelo Zacharias, Trivelin, Paulo Cesar Ocheuze, Bouillet, Jean-Pierre, Grant, Dominique, Nouvellon, Yann
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1093/treephys/tpv090
http://hdl.handle.net/11449/220573
Resumo: Potassium (K) is an important limiting factor of tree growth, but little is known of the effects of K supply on the long-distance transport of photosynthetic carbon (C) in the phloem and of the interaction between K fertilization and drought. We pulse-labelled 2-year-old Eucalyptus grandis L. trees grown in a field trial combining K fertilization (+K and -K) and throughfall exclusion (+W and -W), and we estimated the velocity of C transfer by comparing time lags between the uptake of 13CO2 and its recovery in trunk CO2 efflux recorded at different heights. We also analysed the dynamics of the labelled photosynthates recovered in the foliage and in the phloem sap (inner bark extract). The mean residence time of labelled C in the foliage was short (21-31 h). The time series of 13C in excess in the foliage was affected by the level of fertilization, whereas the effect of throughfall exclusion was not significant. The velocity of C transfer in the trunk (0.20-0.82mh-1) was twice as high in +K trees than in -K trees, with no significant effect of throughfall exclusion except for one +K-W tree labelled in the middle of the drought season that was exposed to a more pronounced water stress (midday leaf water potential of -2.2MPa). Our results suggest that besides reductions in photosynthetic C supply and in C demand by sink organs, the lower velocity under K deficiency is due to a lower cross-sectional area of the sieve tubes, whereas an increase in phloem sap viscosity is more likely limiting phloem transport under drought. In all treatments, 10 times less 13C was recovered in inner bark extracts at the bottom of the trunk when compared with the base of the crown, suggesting that a large part of the labelled assimilates has been exported out of the phloem and replaced by unlabelled C. This supports the 'leakage-retrieval mechanism' that may play a role in maintaining the pressure gradient between source and sink organs required to sustain high velocity of phloem transport in tall trees.
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spelling In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carboncarbon isotopecarbon transferdroughtEucalyptus grandisfertilizationPotassium (K) is an important limiting factor of tree growth, but little is known of the effects of K supply on the long-distance transport of photosynthetic carbon (C) in the phloem and of the interaction between K fertilization and drought. We pulse-labelled 2-year-old Eucalyptus grandis L. trees grown in a field trial combining K fertilization (+K and -K) and throughfall exclusion (+W and -W), and we estimated the velocity of C transfer by comparing time lags between the uptake of 13CO2 and its recovery in trunk CO2 efflux recorded at different heights. We also analysed the dynamics of the labelled photosynthates recovered in the foliage and in the phloem sap (inner bark extract). The mean residence time of labelled C in the foliage was short (21-31 h). The time series of 13C in excess in the foliage was affected by the level of fertilization, whereas the effect of throughfall exclusion was not significant. The velocity of C transfer in the trunk (0.20-0.82mh-1) was twice as high in +K trees than in -K trees, with no significant effect of throughfall exclusion except for one +K-W tree labelled in the middle of the drought season that was exposed to a more pronounced water stress (midday leaf water potential of -2.2MPa). Our results suggest that besides reductions in photosynthetic C supply and in C demand by sink organs, the lower velocity under K deficiency is due to a lower cross-sectional area of the sieve tubes, whereas an increase in phloem sap viscosity is more likely limiting phloem transport under drought. In all treatments, 10 times less 13C was recovered in inner bark extracts at the bottom of the trunk when compared with the base of the crown, suggesting that a large part of the labelled assimilates has been exported out of the phloem and replaced by unlabelled C. This supports the 'leakage-retrieval mechanism' that may play a role in maintaining the pressure gradient between source and sink organs required to sustain high velocity of phloem transport in tall trees.UMR 1137 Ecologie et Ecophysiologie Forestières Facult des Sciences Universit de LorraineINRA UMR 1137 Ecologie et Ecophysiologie Forestières Centre de NancyCIRAD UMR Ecoandsols Ecologie Fonctionnelle and Biogochimie des Sols and Agro-cosystèmesEmbrapa Meio AmbienteUniversidade Estadual de São PauloDepartamento de Ciências Florestais ESALQ Universidade de São Paulo ESALQLaboratory of Forest Utilization Department of Forest and Biomaterial Science Graduate School of Agriculture Kyoto UniversityCentro de Energia Nuclear Na Agricultura Universidade de São PauloDepartamento de Ciências Atmosfricas IAG Universidade de São Paulo ESALQUniversidade Estadual de São PauloUniversit de LorraineCentre de NancyEcologie Fonctionnelle and Biogochimie des Sols and Agro-cosystèmesEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)Universidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)Kyoto UniversityEpron, DanielCabral, Osvaldo Machado RodriguesLaclau, Jean-Paul [UNESP]Dannoura, MasakoPacker, Ana PaulaPlain, CarolineBattie-Laclau, PatriciaMoreira, Marcelo ZachariasTrivelin, Paulo Cesar OcheuzeBouillet, Jean-PierreGrant, DominiqueNouvellon, Yann2022-04-28T19:03:00Z2022-04-28T19:03:00Z2015-08-11info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article6-21http://dx.doi.org/10.1093/treephys/tpv090Tree Physiology, v. 36, n. 1, p. 6-21, 2015.1758-44690829-318Xhttp://hdl.handle.net/11449/22057310.1093/treephys/tpv0902-s2.0-84959881063Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengTree Physiologyinfo:eu-repo/semantics/openAccess2022-04-28T19:03:00Zoai:repositorio.unesp.br:11449/220573Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:38:43.177969Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carbon
title In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carbon
spellingShingle In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carbon
Epron, Daniel
carbon isotope
carbon transfer
drought
Eucalyptus grandis
fertilization
title_short In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carbon
title_full In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carbon
title_fullStr In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carbon
title_full_unstemmed In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carbon
title_sort In situ 13CO2 pulse labelling of field-grown eucalypt trees revealed the effects of potassium nutrition and throughfall exclusion on phloem transport of photosynthetic carbon
author Epron, Daniel
author_facet Epron, Daniel
Cabral, Osvaldo Machado Rodrigues
Laclau, Jean-Paul [UNESP]
Dannoura, Masako
Packer, Ana Paula
Plain, Caroline
Battie-Laclau, Patricia
Moreira, Marcelo Zacharias
Trivelin, Paulo Cesar Ocheuze
Bouillet, Jean-Pierre
Grant, Dominique
Nouvellon, Yann
author_role author
author2 Cabral, Osvaldo Machado Rodrigues
Laclau, Jean-Paul [UNESP]
Dannoura, Masako
Packer, Ana Paula
Plain, Caroline
Battie-Laclau, Patricia
Moreira, Marcelo Zacharias
Trivelin, Paulo Cesar Ocheuze
Bouillet, Jean-Pierre
Grant, Dominique
Nouvellon, Yann
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universit de Lorraine
Centre de Nancy
Ecologie Fonctionnelle and Biogochimie des Sols and Agro-cosystèmes
Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA)
Universidade Estadual Paulista (UNESP)
Universidade de São Paulo (USP)
Kyoto University
dc.contributor.author.fl_str_mv Epron, Daniel
Cabral, Osvaldo Machado Rodrigues
Laclau, Jean-Paul [UNESP]
Dannoura, Masako
Packer, Ana Paula
Plain, Caroline
Battie-Laclau, Patricia
Moreira, Marcelo Zacharias
Trivelin, Paulo Cesar Ocheuze
Bouillet, Jean-Pierre
Grant, Dominique
Nouvellon, Yann
dc.subject.por.fl_str_mv carbon isotope
carbon transfer
drought
Eucalyptus grandis
fertilization
topic carbon isotope
carbon transfer
drought
Eucalyptus grandis
fertilization
description Potassium (K) is an important limiting factor of tree growth, but little is known of the effects of K supply on the long-distance transport of photosynthetic carbon (C) in the phloem and of the interaction between K fertilization and drought. We pulse-labelled 2-year-old Eucalyptus grandis L. trees grown in a field trial combining K fertilization (+K and -K) and throughfall exclusion (+W and -W), and we estimated the velocity of C transfer by comparing time lags between the uptake of 13CO2 and its recovery in trunk CO2 efflux recorded at different heights. We also analysed the dynamics of the labelled photosynthates recovered in the foliage and in the phloem sap (inner bark extract). The mean residence time of labelled C in the foliage was short (21-31 h). The time series of 13C in excess in the foliage was affected by the level of fertilization, whereas the effect of throughfall exclusion was not significant. The velocity of C transfer in the trunk (0.20-0.82mh-1) was twice as high in +K trees than in -K trees, with no significant effect of throughfall exclusion except for one +K-W tree labelled in the middle of the drought season that was exposed to a more pronounced water stress (midday leaf water potential of -2.2MPa). Our results suggest that besides reductions in photosynthetic C supply and in C demand by sink organs, the lower velocity under K deficiency is due to a lower cross-sectional area of the sieve tubes, whereas an increase in phloem sap viscosity is more likely limiting phloem transport under drought. In all treatments, 10 times less 13C was recovered in inner bark extracts at the bottom of the trunk when compared with the base of the crown, suggesting that a large part of the labelled assimilates has been exported out of the phloem and replaced by unlabelled C. This supports the 'leakage-retrieval mechanism' that may play a role in maintaining the pressure gradient between source and sink organs required to sustain high velocity of phloem transport in tall trees.
publishDate 2015
dc.date.none.fl_str_mv 2015-08-11
2022-04-28T19:03:00Z
2022-04-28T19:03:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1093/treephys/tpv090
Tree Physiology, v. 36, n. 1, p. 6-21, 2015.
1758-4469
0829-318X
http://hdl.handle.net/11449/220573
10.1093/treephys/tpv090
2-s2.0-84959881063
url http://dx.doi.org/10.1093/treephys/tpv090
http://hdl.handle.net/11449/220573
identifier_str_mv Tree Physiology, v. 36, n. 1, p. 6-21, 2015.
1758-4469
0829-318X
10.1093/treephys/tpv090
2-s2.0-84959881063
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Tree Physiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 6-21
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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