Metals in Arc Magmas: The Role of Cu-Rich Sulfide Phases

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dc.contributor.advisorCandela, Philip Aen_US
dc.contributor.advisorPiccoli, Philip Men_US
dc.contributor.authorMengason, Michael Jamesen_US
dc.contributor.departmentGeologyen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2012-02-17T06:45:08Z
dc.date.available2012-02-17T06:45:08Z
dc.date.issued2011en_US
dc.description.abstractBased on experiments performed on hydrous andesitic melts at 1000°C, 150 MPa, <italic>f</italic>O<subscript>2</subscript> from the Co-CoO to Ni-NiO buffer, and log <italic>f</italic>S<subscript>2</subscript> equal to -0.5 to -1.5 (bar), greater than 32 ± 4 ppm copper (all uncertainties = 1 sigma, standard deviation of the mean) in the silicate melt favors the formation of a Cu-Fe sulfide liquid (CFSL) relative to pyrrhotite at sulfide saturation. This concentration is well within the range encountered in intrusive and extrusive rocks suggesting that saturation by sulfide liquids is a common occurrence in magmatic arc systems consistent with observations in naturally occurring andesites. Nernst-type partition coefficients determined from these experiments highlight the importance of accurately modeling the composition of the sulfide phase present during partial melting or fractional crystallization: D<superscript>pyrrhotite/melt </superscript>= 1320 ± 220 for Cu, 1.73 ± 0.37 for Mo, 90 ± 19 for Ag, and 500 ± 87 for Au, whereas D<superscript>CFSL/melt </superscript>= 7,800 ± 1,400 for Cu, 0.45 ± 0.14 for Mo, 6,800 ± 1,300 for Ag, and 84,000 ± 19,000 for Au. Data from these experiments support a direct correlation between the solubility of gold and the concentration of sulfur in the silicate melt at low <italic>f</italic>O<subscript>2</subscript>, as well as a dependence of the solubility of gold on <italic>f</italic>S<subscript>2</subscript><superscript>0.25</superscript> in pyrrhotite and CFSL. As a part of this research, pyrrhotite of variable copper concentration was equilibrated at 1000°C in sealed evacuated silica tubes to determine a method that allows the equation of Toulmin and Barton (1964) to be used to calculate <italic>f</italic>S<subscript>2</subscript> for Cu-bearing pyrrhotite. This method is consistent for pyrrhotite with up to 6 wt % Cu by using N=2*[(XCu+XFe)/(1.5XCu+XFe+XS)]. These data suggest that separation of CFSL from the magma along with crystalline phases during fractional crystallization can reduce the likelihood of magmatic hydrothermal ore formation. For example, modeling 30 % Rayleigh fractional crystallization (F=1.0 to F=0.7), with 0.1% sulfide among the separating phases, and an initial 65 ppm Cu in the silicate melt, would result in the sequestration of up to 50% of the initial Ag, 60 % Cu, and > 99 % Au.en_US
dc.identifier.urihttp://hdl.handle.net/1903/12256
dc.subject.pqcontrolledGeologyen_US
dc.subject.pqcontrolledPetrologyen_US
dc.subject.pqcontrolledGeochemistryen_US
dc.subject.pquncontrolledExperimentalen_US
dc.subject.pquncontrolledMagmaen_US
dc.subject.pquncontrolledPartition coefficientsen_US
dc.subject.pquncontrolledPorphyry deposten_US
dc.subject.pquncontrolledSubduction Zoneen_US
dc.subject.pquncontrolledSulfideen_US
dc.titleMetals in Arc Magmas: The Role of Cu-Rich Sulfide Phasesen_US
dc.typeDissertationen_US

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