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Servicio de Geología,Minas de Almadén y Arrayanes S. A., 13400 Almadén, Spain

Department of Geology and Geophysics, University of Adelaide, Adelaide, Australia 5005
Departamento de Ingeniería Geológica, Escuela Técnica Superior de Ingenieros de Minas, Ríos Rosas 21, 28003 Madrid, Spain
Scottish Universities Environmental Research Centre, East Kilbride, Scotland G75 OQF
Departamento de Física, Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas, Spain
Departamento de Geología, Universidad de Oviedo, Jesús Arias de Velasco s/n, 3305 Oviedo, Spain
Corresponding author: e-mail, ross.both{at}adelaide.edu.au
The Alcudia Valley is intensely mineralized, with a large number of Pb-Zn-Ag-Cu deposits hosted by Neoproterozoic and Paleozoic sedimentary rocks. Five distinct types of deposits have been recognized. The most significant mineralizing events were related to the two major phases of deformation (HD1, HD2) and granite emplacement during the Hercynian orogeny. Stable isotope and lithogeochemical data demonstrate that the metals, as well as sulfur and carbon, were sourced from the local sedimentary rocks.
Type A deposits are minor occurrences of strata-bound mineralization with Zn > Pb, occurring as disseminations and small veins in Late Ordovician limestone. A syndiagenetic origin is suggested by the limited stratigraphic distribution of the mineralization and anomalous base metal contents of Late Ordovician-Early Silurian black shales overlying the mineralized limestone. Minor remobilization of disseminated sulfides into joints took place during late diagenesis or early Hercynian deformation.
Types B, C, and D are syntectonic deposits with Zn > Pb.
Type B deposits are strongly deformed veins in HD1 fractures in
Ordovician rocks. A process involving local mobilization of metals by a
surface-derived fluid is indicated by depleted metal contents of host rocks
adjacent to the veins, the similarity of
34S values of ore sulfides with
disseminated pyrite in the host rocks, and the
18OH2O values. Type C
deposits exhibit a greater variation in morphology and degree of deformation
compared to other types and are found in both HD1 and HD2
fractures in Late Ordovician and Silurian rocks. The stratigraphic distribution
and
34S values of sulfides are similar to type A deposits, suggesting that
localized hydrothermal systems either remobilized type A mineralization or
derived metals and sulfur from the same source. Type D deposits occur in HD2
shear fractures in Neoproterozoic rocks. The
13C values of carbonate gangue and
the similarity of
34S values of ore sulfides and disseminated pyrite in the
host rocks indicate that black shales of the Neoproterozoic sequence are the
major source of sulfur and carbon. Mixing of a metamorphic fluid with a
surface-derived fluid is suggested by fluid inclusion and oxygen isotope data.
Type E deposits, the most abundant and economically most
important type, are post-tectonic Pb > Zn veins occupying HD2
fractures and are widely distributed through the district in rocks ranging from
Neoproterozoic to Late Ordovician. Mineral assemblages and Ag contents of the
veins show a zonal relationship with respect to monzogranite outcrops,
indicating that late Hercynian magmatism was the source of heat driving fluid
migration through the fracture system. Fluid inclusion and oxygen isotope data
are typical of basinal brines. Reaction of the fluid with black shales of the
Neoproterozoic sequence is suggested by
34S values of sulfides and
13C values
of carbonates of the main stages of the paragenetic sequence. The final
paragenetic stage consists of barite, calcite, and pyrite, which may have been
deposited during a later hydrothermal event, probably in the Early Triassic.
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