Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)

Autores
Menzel, Manuel D.; Garrido, Carlos J.; López Sánchez Vizcaíno, Vicente; Marchesi, Claudio; Hidas, Károly; Escayola, Monica Patricia; Delgado Huertas, Antonio
Año de publicación
2018
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The mantle section of the Advocate ophiolite (Newfoundland, Canada) contains unique outcrops of listvenite (magnesite-quartz), antigorite- and quartz-bearing talc-magnesite rock, and carbonated antigorite-serpentinite. This lithological sequence records the sequential carbonation of serpentinite by CO2-rich hydrothermal fluids. High Cr and Ni contents and preservation of Cr-spinel with a composition similar to that of Atg-serpentinite (molar Mg/Mg + Fe = 0.50–0.65; Cr/Cr + Al = 0.50–0.70), show that the Advocate listvenite and talc-magnesite rocks formed by carbonation of variably serpentinized mantle harzburgite. Replacement of lizardite by magnesite coeval with the breakdown of lizardite to antigorite + brucite and the lack of prograde olivine and magnetite in antigorite serpentinite and talc-magnesite rocks constrain the temperature of carbonation between c. 280 °C and 420 °C. Thermodynamic modelling of carbonation of serpentinite at 300 °C and 0.2–0.5 GPa accounts for the sequence of carbonated rocks in the Advocate complex. Phase relations and petrological observations indicate that the aqueous aSiO2 and aCO2 of the infiltrating CO2-rich fluid were buffered at the Atg-Tlc-Mgs and Qtz-Tlc-Mgs pseudo-invariant points, forming dominantly three-phase rocks by variable extents of carbonation at these pseudo-invariant points. Listvenites formed at large fluid-rock ratio when quartz became saturated in the fluid and precipitated along magnesite grain boundaries and in variably sized tensional veins. The whole rock Fe3+/Fetotal ratio of the Advocate carbonate-bearing sequence decreases with increasing whole rock carbon content, from 0.65–0.80 in brucite-bearing antigorite serpentinite to 0.10–0.30 in talc-magnesite rocks and listvenite. The whole rock iron reduction is associated with an increase in the ferrous iron content of magnesite and the formation of hematite and goethite, indicating a concomitant increase of the fluid oxygen fugacity. The sequence of carbonation reactions is uniquely preserved in three main growth zones characteristic of listvenite magnesite: (i) an inner zone of magnetite-bearing, Fe-poor, Mn-bearing magnesite formed by carbonation of lizardite, brucite and olivine from Atg-serpentinite; (ii) an outer zone of Fe-rich magnesite formed by carbonation of antigorite and in equilibrium with Fe-poor talc; and (iii) an outermost rim of Fe-poor magnesite formed by carbonation of talc. We propose that carbonation of the Advocate serpentinized mantle harzburgite occurred in a supra-subduction upper plate ophiolite by fluxing of slab-derived, CO2-rich fluids channelled along deep faults at the onset of accretion of the forearc basin (c. 300 °C, <0.5 GPa). The rather constant δ18O (11.0–14.4‰ V-SMOW) and relatively low δ13C (−8.9 to −5.0‰ V-PDB) of magnesite throughout the sequence of carbonated rocks in the Advocate complex is consistent with CO2-rich fluids derived from decarbonation or dissolution of organic carbon- and carbonate-bearing meta-sediments, such as those occurring in the underlying Birchy complex — the partially subducted continental margin of Laurentia. Carbonation of serpentinized oceanic or continental mantle lithosphere by reactive percolation of CO2-rich fluids derived from the slab in forearc settings may represent a significant carbon reservoir for the deep carbon cycle.
Fil: Menzel, Manuel D.. Instituto Andaluz de Ciencias de la Tierra ; España
Fil: Garrido, Carlos J.. Instituto Andaluz de Ciencias de la Tierra; España
Fil: López Sánchez Vizcaíno, Vicente. Universidad de Jaén; España
Fil: Marchesi, Claudio. Instituto Andaluz de Ciencias de la Tierra ; España. Universidad de Granada; España
Fil: Hidas, Károly. Instituto Andaluz de Ciencias de la Tierra ; España
Fil: Escayola, Monica Patricia. Universidad Nacional de Tierra del Fuego, Antártida e Islas del Atlántico Sur. Instituto de Ciencias Polares, Ambientales y Recursos Naturales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Delgado Huertas, Antonio. Instituto Andaluz de Ciencias de la Tierra ; España
Materia
ADVOCATE COMPLEX
CO2 SEQUESTRATION
FOREARC
LISTVENITE
PERIDOTITE CARBONATION
SERPENTINIZATION
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/118043

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network_name_str CONICET Digital (CONICET)
spelling Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)Menzel, Manuel D.Garrido, Carlos J.López Sánchez Vizcaíno, VicenteMarchesi, ClaudioHidas, KárolyEscayola, Monica PatriciaDelgado Huertas, AntonioADVOCATE COMPLEXCO2 SEQUESTRATIONFOREARCLISTVENITEPERIDOTITE CARBONATIONSERPENTINIZATIONhttps://purl.org/becyt/ford/1.5https://purl.org/becyt/ford/1The mantle section of the Advocate ophiolite (Newfoundland, Canada) contains unique outcrops of listvenite (magnesite-quartz), antigorite- and quartz-bearing talc-magnesite rock, and carbonated antigorite-serpentinite. This lithological sequence records the sequential carbonation of serpentinite by CO2-rich hydrothermal fluids. High Cr and Ni contents and preservation of Cr-spinel with a composition similar to that of Atg-serpentinite (molar Mg/Mg + Fe = 0.50–0.65; Cr/Cr + Al = 0.50–0.70), show that the Advocate listvenite and talc-magnesite rocks formed by carbonation of variably serpentinized mantle harzburgite. Replacement of lizardite by magnesite coeval with the breakdown of lizardite to antigorite + brucite and the lack of prograde olivine and magnetite in antigorite serpentinite and talc-magnesite rocks constrain the temperature of carbonation between c. 280 °C and 420 °C. Thermodynamic modelling of carbonation of serpentinite at 300 °C and 0.2–0.5 GPa accounts for the sequence of carbonated rocks in the Advocate complex. Phase relations and petrological observations indicate that the aqueous aSiO2 and aCO2 of the infiltrating CO2-rich fluid were buffered at the Atg-Tlc-Mgs and Qtz-Tlc-Mgs pseudo-invariant points, forming dominantly three-phase rocks by variable extents of carbonation at these pseudo-invariant points. Listvenites formed at large fluid-rock ratio when quartz became saturated in the fluid and precipitated along magnesite grain boundaries and in variably sized tensional veins. The whole rock Fe3+/Fetotal ratio of the Advocate carbonate-bearing sequence decreases with increasing whole rock carbon content, from 0.65–0.80 in brucite-bearing antigorite serpentinite to 0.10–0.30 in talc-magnesite rocks and listvenite. The whole rock iron reduction is associated with an increase in the ferrous iron content of magnesite and the formation of hematite and goethite, indicating a concomitant increase of the fluid oxygen fugacity. The sequence of carbonation reactions is uniquely preserved in three main growth zones characteristic of listvenite magnesite: (i) an inner zone of magnetite-bearing, Fe-poor, Mn-bearing magnesite formed by carbonation of lizardite, brucite and olivine from Atg-serpentinite; (ii) an outer zone of Fe-rich magnesite formed by carbonation of antigorite and in equilibrium with Fe-poor talc; and (iii) an outermost rim of Fe-poor magnesite formed by carbonation of talc. We propose that carbonation of the Advocate serpentinized mantle harzburgite occurred in a supra-subduction upper plate ophiolite by fluxing of slab-derived, CO2-rich fluids channelled along deep faults at the onset of accretion of the forearc basin (c. 300 °C, <0.5 GPa). The rather constant δ18O (11.0–14.4‰ V-SMOW) and relatively low δ13C (−8.9 to −5.0‰ V-PDB) of magnesite throughout the sequence of carbonated rocks in the Advocate complex is consistent with CO2-rich fluids derived from decarbonation or dissolution of organic carbon- and carbonate-bearing meta-sediments, such as those occurring in the underlying Birchy complex — the partially subducted continental margin of Laurentia. Carbonation of serpentinized oceanic or continental mantle lithosphere by reactive percolation of CO2-rich fluids derived from the slab in forearc settings may represent a significant carbon reservoir for the deep carbon cycle.Fil: Menzel, Manuel D.. Instituto Andaluz de Ciencias de la Tierra ; EspañaFil: Garrido, Carlos J.. Instituto Andaluz de Ciencias de la Tierra; EspañaFil: López Sánchez Vizcaíno, Vicente. Universidad de Jaén; EspañaFil: Marchesi, Claudio. Instituto Andaluz de Ciencias de la Tierra ; España. Universidad de Granada; EspañaFil: Hidas, Károly. Instituto Andaluz de Ciencias de la Tierra ; EspañaFil: Escayola, Monica Patricia. Universidad Nacional de Tierra del Fuego, Antártida e Islas del Atlántico Sur. Instituto de Ciencias Polares, Ambientales y Recursos Naturales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Delgado Huertas, Antonio. Instituto Andaluz de Ciencias de la Tierra ; EspañaElsevier Science2018-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/118043Menzel, Manuel D.; Garrido, Carlos J.; López Sánchez Vizcaíno, Vicente; Marchesi, Claudio; Hidas, Károly; et al.; Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada); Elsevier Science; Lithos; 323; 6-2018; 238-2610024-4937CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0024493718302007?via%3Dihubinfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.lithos.2018.06.001info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:00:49Zoai:ri.conicet.gov.ar:11336/118043instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:00:49.732CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)
title Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)
spellingShingle Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)
Menzel, Manuel D.
ADVOCATE COMPLEX
CO2 SEQUESTRATION
FOREARC
LISTVENITE
PERIDOTITE CARBONATION
SERPENTINIZATION
title_short Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)
title_full Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)
title_fullStr Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)
title_full_unstemmed Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)
title_sort Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada)
dc.creator.none.fl_str_mv Menzel, Manuel D.
Garrido, Carlos J.
López Sánchez Vizcaíno, Vicente
Marchesi, Claudio
Hidas, Károly
Escayola, Monica Patricia
Delgado Huertas, Antonio
author Menzel, Manuel D.
author_facet Menzel, Manuel D.
Garrido, Carlos J.
López Sánchez Vizcaíno, Vicente
Marchesi, Claudio
Hidas, Károly
Escayola, Monica Patricia
Delgado Huertas, Antonio
author_role author
author2 Garrido, Carlos J.
López Sánchez Vizcaíno, Vicente
Marchesi, Claudio
Hidas, Károly
Escayola, Monica Patricia
Delgado Huertas, Antonio
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv ADVOCATE COMPLEX
CO2 SEQUESTRATION
FOREARC
LISTVENITE
PERIDOTITE CARBONATION
SERPENTINIZATION
topic ADVOCATE COMPLEX
CO2 SEQUESTRATION
FOREARC
LISTVENITE
PERIDOTITE CARBONATION
SERPENTINIZATION
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.5
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The mantle section of the Advocate ophiolite (Newfoundland, Canada) contains unique outcrops of listvenite (magnesite-quartz), antigorite- and quartz-bearing talc-magnesite rock, and carbonated antigorite-serpentinite. This lithological sequence records the sequential carbonation of serpentinite by CO2-rich hydrothermal fluids. High Cr and Ni contents and preservation of Cr-spinel with a composition similar to that of Atg-serpentinite (molar Mg/Mg + Fe = 0.50–0.65; Cr/Cr + Al = 0.50–0.70), show that the Advocate listvenite and talc-magnesite rocks formed by carbonation of variably serpentinized mantle harzburgite. Replacement of lizardite by magnesite coeval with the breakdown of lizardite to antigorite + brucite and the lack of prograde olivine and magnetite in antigorite serpentinite and talc-magnesite rocks constrain the temperature of carbonation between c. 280 °C and 420 °C. Thermodynamic modelling of carbonation of serpentinite at 300 °C and 0.2–0.5 GPa accounts for the sequence of carbonated rocks in the Advocate complex. Phase relations and petrological observations indicate that the aqueous aSiO2 and aCO2 of the infiltrating CO2-rich fluid were buffered at the Atg-Tlc-Mgs and Qtz-Tlc-Mgs pseudo-invariant points, forming dominantly three-phase rocks by variable extents of carbonation at these pseudo-invariant points. Listvenites formed at large fluid-rock ratio when quartz became saturated in the fluid and precipitated along magnesite grain boundaries and in variably sized tensional veins. The whole rock Fe3+/Fetotal ratio of the Advocate carbonate-bearing sequence decreases with increasing whole rock carbon content, from 0.65–0.80 in brucite-bearing antigorite serpentinite to 0.10–0.30 in talc-magnesite rocks and listvenite. The whole rock iron reduction is associated with an increase in the ferrous iron content of magnesite and the formation of hematite and goethite, indicating a concomitant increase of the fluid oxygen fugacity. The sequence of carbonation reactions is uniquely preserved in three main growth zones characteristic of listvenite magnesite: (i) an inner zone of magnetite-bearing, Fe-poor, Mn-bearing magnesite formed by carbonation of lizardite, brucite and olivine from Atg-serpentinite; (ii) an outer zone of Fe-rich magnesite formed by carbonation of antigorite and in equilibrium with Fe-poor talc; and (iii) an outermost rim of Fe-poor magnesite formed by carbonation of talc. We propose that carbonation of the Advocate serpentinized mantle harzburgite occurred in a supra-subduction upper plate ophiolite by fluxing of slab-derived, CO2-rich fluids channelled along deep faults at the onset of accretion of the forearc basin (c. 300 °C, <0.5 GPa). The rather constant δ18O (11.0–14.4‰ V-SMOW) and relatively low δ13C (−8.9 to −5.0‰ V-PDB) of magnesite throughout the sequence of carbonated rocks in the Advocate complex is consistent with CO2-rich fluids derived from decarbonation or dissolution of organic carbon- and carbonate-bearing meta-sediments, such as those occurring in the underlying Birchy complex — the partially subducted continental margin of Laurentia. Carbonation of serpentinized oceanic or continental mantle lithosphere by reactive percolation of CO2-rich fluids derived from the slab in forearc settings may represent a significant carbon reservoir for the deep carbon cycle.
Fil: Menzel, Manuel D.. Instituto Andaluz de Ciencias de la Tierra ; España
Fil: Garrido, Carlos J.. Instituto Andaluz de Ciencias de la Tierra; España
Fil: López Sánchez Vizcaíno, Vicente. Universidad de Jaén; España
Fil: Marchesi, Claudio. Instituto Andaluz de Ciencias de la Tierra ; España. Universidad de Granada; España
Fil: Hidas, Károly. Instituto Andaluz de Ciencias de la Tierra ; España
Fil: Escayola, Monica Patricia. Universidad Nacional de Tierra del Fuego, Antártida e Islas del Atlántico Sur. Instituto de Ciencias Polares, Ambientales y Recursos Naturales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Delgado Huertas, Antonio. Instituto Andaluz de Ciencias de la Tierra ; España
description The mantle section of the Advocate ophiolite (Newfoundland, Canada) contains unique outcrops of listvenite (magnesite-quartz), antigorite- and quartz-bearing talc-magnesite rock, and carbonated antigorite-serpentinite. This lithological sequence records the sequential carbonation of serpentinite by CO2-rich hydrothermal fluids. High Cr and Ni contents and preservation of Cr-spinel with a composition similar to that of Atg-serpentinite (molar Mg/Mg + Fe = 0.50–0.65; Cr/Cr + Al = 0.50–0.70), show that the Advocate listvenite and talc-magnesite rocks formed by carbonation of variably serpentinized mantle harzburgite. Replacement of lizardite by magnesite coeval with the breakdown of lizardite to antigorite + brucite and the lack of prograde olivine and magnetite in antigorite serpentinite and talc-magnesite rocks constrain the temperature of carbonation between c. 280 °C and 420 °C. Thermodynamic modelling of carbonation of serpentinite at 300 °C and 0.2–0.5 GPa accounts for the sequence of carbonated rocks in the Advocate complex. Phase relations and petrological observations indicate that the aqueous aSiO2 and aCO2 of the infiltrating CO2-rich fluid were buffered at the Atg-Tlc-Mgs and Qtz-Tlc-Mgs pseudo-invariant points, forming dominantly three-phase rocks by variable extents of carbonation at these pseudo-invariant points. Listvenites formed at large fluid-rock ratio when quartz became saturated in the fluid and precipitated along magnesite grain boundaries and in variably sized tensional veins. The whole rock Fe3+/Fetotal ratio of the Advocate carbonate-bearing sequence decreases with increasing whole rock carbon content, from 0.65–0.80 in brucite-bearing antigorite serpentinite to 0.10–0.30 in talc-magnesite rocks and listvenite. The whole rock iron reduction is associated with an increase in the ferrous iron content of magnesite and the formation of hematite and goethite, indicating a concomitant increase of the fluid oxygen fugacity. The sequence of carbonation reactions is uniquely preserved in three main growth zones characteristic of listvenite magnesite: (i) an inner zone of magnetite-bearing, Fe-poor, Mn-bearing magnesite formed by carbonation of lizardite, brucite and olivine from Atg-serpentinite; (ii) an outer zone of Fe-rich magnesite formed by carbonation of antigorite and in equilibrium with Fe-poor talc; and (iii) an outermost rim of Fe-poor magnesite formed by carbonation of talc. We propose that carbonation of the Advocate serpentinized mantle harzburgite occurred in a supra-subduction upper plate ophiolite by fluxing of slab-derived, CO2-rich fluids channelled along deep faults at the onset of accretion of the forearc basin (c. 300 °C, <0.5 GPa). The rather constant δ18O (11.0–14.4‰ V-SMOW) and relatively low δ13C (−8.9 to −5.0‰ V-PDB) of magnesite throughout the sequence of carbonated rocks in the Advocate complex is consistent with CO2-rich fluids derived from decarbonation or dissolution of organic carbon- and carbonate-bearing meta-sediments, such as those occurring in the underlying Birchy complex — the partially subducted continental margin of Laurentia. Carbonation of serpentinized oceanic or continental mantle lithosphere by reactive percolation of CO2-rich fluids derived from the slab in forearc settings may represent a significant carbon reservoir for the deep carbon cycle.
publishDate 2018
dc.date.none.fl_str_mv 2018-06
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/118043
Menzel, Manuel D.; Garrido, Carlos J.; López Sánchez Vizcaíno, Vicente; Marchesi, Claudio; Hidas, Károly; et al.; Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada); Elsevier Science; Lithos; 323; 6-2018; 238-261
0024-4937
CONICET Digital
CONICET
url http://hdl.handle.net/11336/118043
identifier_str_mv Menzel, Manuel D.; Garrido, Carlos J.; López Sánchez Vizcaíno, Vicente; Marchesi, Claudio; Hidas, Károly; et al.; Carbonation of mantle peridotite by CO2-rich fluids: the formation of listvenites in the Advocate ophiolite complex (Newfoundland, Canada); Elsevier Science; Lithos; 323; 6-2018; 238-261
0024-4937
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0024493718302007?via%3Dihub
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.lithos.2018.06.001
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
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dc.publisher.none.fl_str_mv Elsevier Science
publisher.none.fl_str_mv Elsevier Science
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
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instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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