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dc.contributor.authorEsteban-Arispe, Iñaki
dc.contributor.authorBoyce, Adrian J.
dc.contributor.authorCarrillo Rosúa, Francisco Javier 
dc.contributor.authorMorales Ruano, Salvador 
dc.contributor.authorVelasco, Francisco
dc.contributor.authorYusta, Iñaki
dc.date.accessioned2015-04-07T07:00:56Z
dc.date.available2015-04-07T07:00:56Z
dc.date.issued2009-06
dc.identifier.citationEsteban-Arispe, I.; Boyce, A.J.; Carrillo-Rosúa, J.; Morales-Ruano, S.; Velasco, F.; Yusta, I. Geochemistry of the Zn-Pb-Cu-(Ag)-(Au) epithermal deposits from San José (SE Spain). Geochimica et Cosmochimica Acta, 73(13): A339-A339 (2009). [http://hdl.handle.net/10481/35430]es_ES
dc.identifier.issn0016-7037
dc.identifier.urihttp://hdl.handle.net/10481/35430
dc.descriptionVersión preprintes_ES
dc.descriptionAbstracts of the 19th Annual V.M. Goldschmidt Conference (2009): "Challenges to our volatile planet". June 21-26 in Davos (Switzerland).es_ES
dc.description.abstractThe San José Zn-Pb-Cu-(Ag-Au) vein systems, previously described as low-sulfidation [1], are located in the Cabo de Gata Volcanic Field (SE Spain). These deposits comprise mainly base metal bearing sulfide/sulfosalts quartz veins, while disseminated pyrite with small quantities of gold appear in areas of vuggy silica alteration. Wallrock alteration includes silicification, advanced argillic, argillic and propylitic zones. Very abundant, penetrative, stockwork-like Fe-Al sulfate veins are found in the argillic and advanced argillic alteration, but ore veins do not show a clear relationship with the alteration zone. Mass balance using the isocone method reveals a gradual lixiviation of most of the elements (except silica) in the highly altered volcanic rocks involving a generalized loss of mass and an increase in the content of some metallic elements (Zn, Pb, Cu) in the less altered zones. Vein sulfides show a similar or slighty heavier sulfur signature (δ34S: 6-12‰) compared to the dominant volcanic signature of the zone (δ34S: 1-7‰[1]), suggesting a magmatic source but with possible incorporation of sea water sulfate via inorganic reduction. Such magamtic input could also be related to the gold mineralization. The barite signature (δ34S: 19-21‰) also supports sea water involvement. Pyrite in silicification shows depleted sulfur (δ34S: 2-6‰) perhaps as product of the disproportionation of magmatic SO2 which produced the acid alteration. Abundant alunite-jarosite has light sulphur (δ34S: 4-10‰), but its abundance and ocurrence rule out a simple supergene origin. Meanwhile, oxygen isotopes in quartz (δ18O: 8-18‰) indicate the likely involvement of magmatic and non-magmatic fluids in ore mineralization. The field, mineralogical and geochemical data suggest a complex mineralization history in the San José area, with evidence of both low and high sulfidation hydrothermal systems and the involvement of magmatic and seawater fluids.es_ES
dc.description.sponsorshipDepartamento de Mineralogía y Petrología (Universidad de Granada). Departamento de Didáctica de las Ciencias Experimentales (Universidad de Granada). Instituto Andaluz de Ciencias de la Tierra (Universidad de Granada- Centro Superior de Investigaciones Científicas)es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.subjectStable isotopeses_ES
dc.subjectEpithermal deposites_ES
dc.subjectCabo de Gataes_ES
dc.subjectAlmería es_ES
dc.titleGeochemistry of the Zn-Pb-Cu-(Ag)-(Au) epithermal deposits from San José (SE Spain)es_ES
dc.typeotheres_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.gca.2009.05.005


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