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

被引:0
|
作者
Gonzalez-Jimenez, Jose M. [1 ]
Blanco-Quintero, Idael F. [2 ]
Yesares, Lola [3 ]
Marchesi, Claudio [4 ]
Ferreira, Amira R. [1 ]
Gonzalez-Perez, Igor [4 ]
Schettino, Erwin [5 ]
Cantizano, Francisco Abel Jimenez [6 ]
Gervilla, Fernando [4 ]
机构
[1] CSIC, Inst Andaluz Ciencias Tierra IACT, Avda Palmeras 4, Armilla 18100, Granada, Spain
[2] Univ Alicante, Dept Ciencias Tierra & Medio Ambiente, Ciencias 3, Carretera San Vicente del Raspeig S-N, Alicante 03690, Spain
[3] Univ Complutense Madrid, Fac Ciencias Geol, Dept Mineral & Petrol, C Jose Antonio Novais 12,Ciudad Univ, Madrid 28040, Spain
[4] Univ Granada, Fac Ciencias, Dept Mineral & Petrol, Avda Fuentenueva S-N, Granada 18002, Spain
[5] Swiss Fed Inst Technol, Inst Geochem & Petrol, Clausiusstr 25, CH-8092 Zurich, Switzerland
[6] Junta Andalucia, Agencia Medio Ambiente & Agua, Seville 41092, Spain
关键词
NI-S SYSTEM; MONOSULFIDE SOLID-SOLUTION; PLATINUM-GROUP ELEMENTS; CU-PGE DEPOSIT; PHASE-RELATIONS; LOW-TEMPERATURE; FRACTIONAL CRYSTALLIZATION; HYDROTHERMAL FLUID; CRYSTAL-STRUCTURE; BUSHVELD COMPLEX;
D O I
10.5194/ejm-37-191-2025
中图分类号
P57 [矿物学];
学科分类号
070901 ;
摘要
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)(9)S-8; cubic Fm3m), bounded by tetragonal I (4) over bar 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-fS(2) and high-fO(2) fluids at < 300 degrees C. Tetragonal I<(4)over bar>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 (similar to 200-100 degrees 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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页码:191 / 220
页数:30
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