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
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , , , , , |
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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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 |
|
_version_ |
1808128959061164032 |