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Autordc.contributor.authorReal, Irene del
Autordc.contributor.authorReich Morales, Martín Herbert
Autordc.contributor.authorSimon, Adam C.
Autordc.contributor.authorDeditius, Artur
Autordc.contributor.authorBarra Pantoja, Luis Fernando
Autordc.contributor.authorRodríguez Mustafa, María A.
Autordc.contributor.authorThompson, John F. H.
Autordc.contributor.authorRoberts, Malcolm P.
Fecha ingresodc.date.accessioned2022-06-30T22:03:17Z
Fecha disponibledc.date.available2022-06-30T22:03:17Z
Fecha de publicacióndc.date.issued2021
Cita de ítemdc.identifier.citationCommunications Earth & Environment (2021) 2:192es_ES
Identificadordc.identifier.other10.1038/s43247-021-00265-w
Identificadordc.identifier.urihttps://repositorio.uchile.cl/handle/2250/186385
Resumendc.description.abstractThe Candelaria iron oxide-copper-gold deposit in Chile was formed by superimposed, episodic hydrothermal pulses with contrasting composition and temperature, according to micro-textural and compositional variations in actinolite, a common alteration mineral. Iron oxide-copper-gold deposits are a globally important source of copper, gold and critical commodities. However, they possess a range of characteristics related to a variety of tectono-magmatic settings that make development of a general genetic model challenging. Here we investigate micro-textural and compositional variations in actinolite, to constrain the thermal evolution of the Candelaria iron oxide-copper-gold deposit in Chile. We identify at least two mineralization stages comprising an early 675-800 degrees C iron oxide-apatite type mineralization overprinted by a later copper-rich fluid at around 550-700 degrees C. We propose that these distinct stages were caused by episodic pulses of injection of magmatic-hydrothermal fluids from crystallizing magmas at depth. We suggest that the mineralisation stages we identify were the result of temperature gradients attributable to changes in the magmatic source, rather than variations in formation depth, and that actinolite chemistry can be used as a proxy for formation temperature in iron oxide-copper-gold systems.es_ES
Patrocinadordc.description.sponsorshipANID through Millennium Science Initiative Program NCN13_065 Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) CONICYT FONDECYT 3200532 ANID through FONDECYT grant 1190105 National Science Foundation (NSF) 1924142es_ES
Idiomadc.language.isoenes_ES
Publicadordc.publisherSpringernature, Englandes_ES
Tipo de licenciadc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link a Licenciadc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Fuentedc.sourceCommunications Earth & Environmentes_ES
Palabras clavesdc.subjectCarajas mineral provincees_ES
Palabras clavesdc.subjectO Stable-isotopeses_ES
Palabras clavesdc.subjectAu-ag deposites_ES
Palabras clavesdc.subjectApatite ioaes_ES
Palabras clavesdc.subjectIocg deposites_ES
Palabras clavesdc.subjectNorthwest-territorieses_ES
Palabras clavesdc.subjectStructural controlses_ES
Palabras clavesdc.subjectSulfur isotopeses_ES
Palabras clavesdc.subjectProminent hilles_ES
Palabras clavesdc.subjectGawler cratones_ES
Títulodc.titleFormation of giant iron oxide-copper-gold deposits by superimposed, episodic hydrothermal pulseses_ES
Tipo de documentodc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogadoruchile.catalogadorcfres_ES
Indizaciónuchile.indexArtículo de publícación WoSes_ES
Indizaciónuchile.indexArtículo de publicación SCOPUSes_ES


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Attribution-NonCommercial-NoDerivs 3.0 United States
Excepto que se indique lo contrario, la licencia de este artículo se describe como Attribution-NonCommercial-NoDerivs 3.0 United States