Sulfide mineralogy of igneous basic rocks (ophites) from the external zone of the Betic Cordillera

Abstract. The Triassic sedimentary rocks of the external zone of the Betic Cordillera in southern Spain host abundant igneous basic rocks (“ophites”) metamorphosed in the greenschist facies. Investigation based on high-resolution transmission electron microscopy (HRTEM) reveals magmatic sulfides intimately intergrown with primary silicates (pyroxene, plagioclase and olivine), consisting of pyrrhotite (FeS to Fe7S8; monoclinic C2/c polytype 4C) and pentlandite ((FeNi)9S8; cubic Fm3m), bounded by tetragonal I4‾2d chalcopyrite (CuFeS2). Whole-rock and clinopyroxene geochemical data suggest that Fe–Ni–Cu sulfides crystallized from melt droplets segregated by immiscibility from transitional-alkaline magmas, after their fractional crystallization and volatile oversaturation within crustal conduits developed during intraplate rifting. In contrast, hydrothermal sulfides are pyrite (FeS2) and/or chalcopyrite associated with secondary silicates (chlorite, epidote, saussurite, prehnite, sericite and quartz). Porous pyrite (cubic Pa3) hosts nanodomains of pyrrhotite (monoclinic C2/c polytype 4C and orthorhombic Cmca polytype 11C) and orthorhombic Pnnm marcasite (FeS2), evidencing disulfide formation via coupled Fe loss and S addition in pyrrhotite due to reaction with high-fS2 and high-fO2 fluids at < 300 °C. Tetragonal I4‾2d chalcopyrite replacing pyrite also preserves nanodomains of pyrrhotite as well as of pyrite / marcasite, suggesting reaction of pre-existing Fe sulfides with Cu transported by low-temperature (∼ 200–100 °C) acidic-to-neutral fluids. Additionally, inclusions of sphalerite (ZnS), galena (PbS) and vaesite (NiS2) in pyrite and chalcopyrite spotlight metal remobilization during hydrothermal alteration, which is further confirmed by the crystallization of cobaltite coronas (CoAsS) around pyrite. Our new results contribute to the current debate of the full sequence of processes operating in ore-forming mafic systems.

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Journal
European Journal of Mineralogy
Published
2025-03-20
DOI
https://doi.org/10.5194/ejm-37-191-2025
Primary Topic
Geological and Geophysical Studies Worldwide
Type
article
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article

Sulfide mineralogy of igneous basic rocks (ophites) from the external zone of the Betic Cordillera

Claudio Marchesi, Lola Yesares, Erwin Schettino, Francisco Abel Jiménez-Cantizano et al.
European Journal of Mineralogy
Geological and Geophysical Studies Worldwide
article

Sulfide mineralogy of igneous basic rocks (ophites) from the external zone of the Betic Cordillera

Claudio Marchesi, Lola Yesares, Erwin Schettino, Francisco Abel Jiménez-Cantizano, Igór González-Pérez, Fernando Gervilla, José María González-Jiménez, Idael Francisco Blanco-Quintero, Amira R. Ferreira
article en

Abstract

Abstract. The Triassic sedimentary rocks of the external zone of the Betic Cordillera in southern Spain host abundant igneous basic rocks (“ophites”) metamorphosed in the greenschist facies. Investigation based on high-resolution transmission electron microscopy (HRTEM) reveals magmatic sulfides intimately intergrown with primary silicates (pyroxene, plagioclase and olivine), consisting of pyrrhotite (FeS to Fe7S8; monoclinic C2/c polytype 4C) and pentlandite ((FeNi)9S8; cubic Fm3m), bounded by tetragonal I4‾2d chalcopyrite (CuFeS2). Whole-rock and clinopyroxene geochemical data suggest that Fe–Ni–Cu sulfides crystallized from melt droplets segregated by immiscibility from transitional-alkaline magmas, after their fractional crystallization and volatile oversaturation within crustal conduits developed during intraplate rifting. In contrast, hydrothermal sulfides are pyrite (FeS2) and/or chalcopyrite associated with secondary silicates (chlorite, epidote, saussurite, prehnite, sericite and quartz). Porous pyrite (cubic Pa3) hosts nanodomains of pyrrhotite (monoclinic C2/c polytype 4C and orthorhombic Cmca polytype 11C) and orthorhombic Pnnm marcasite (FeS2), evidencing disulfide formation via coupled Fe loss and S addition in pyrrhotite due to reaction with high-fS2 and high-fO2 fluids at < 300 °C. Tetragonal I4‾2d chalcopyrite replacing pyrite also preserves nanodomains of pyrrhotite as well as of pyrite / marcasite, suggesting reaction of pre-existing Fe sulfides with Cu transported by low-temperature (∼ 200–100 °C) acidic-to-neutral fluids. Additionally, inclusions of sphalerite (ZnS), galena (PbS) and vaesite (NiS2) in pyrite and chalcopyrite spotlight metal remobilization during hydrothermal alteration, which is further confirmed by the crystallization of cobaltite coronas (CoAsS) around pyrite. Our new results contribute to the current debate of the full sequence of processes operating in ore-forming mafic systems.

European Journal of MineralogyVol. 37(2)
Universidad Complutense de Madrid (ES), University of Alicante (ES), Universidad de Granada (ES), Instituto Andaluz de Ciencias de la Tierra (ES), Institute of Geochemistry (CN)
Consejería de Transformación Económica, Industria, Conocimiento y Universidades
Openalex Percentile: Top 91%
Geological and Geophysical Studies Worldwide
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