Sulfide oxidation as a process for the formation of copper-rich magmatic sulfides   总被引：1，自引：0，他引：1  

Cora C. Wohlgemuth-Ueberwasser  Raúl O. C. Fonseca  Chris Ballhaus  Jasper Berndt 《Mineralium Deposita》2013,48(1):115-127

Typical magmatic sulfides are dominated by pyrrhotite and pentlandite with minor chalcopyrite, and the bulk atomic Cu/Fe ratio of these sulfides is typically less than unity. However, there are rare magmatic sulfide occurrences that are dominated by Cu-rich sulfides (e.g., bornite, digenite, and chalcopyrite, sometimes coexisting with metallic Cu) with atomic Cu/Fe as high as 5. Typically, these types of sulfide assemblages occur in the upper parts of moderately to highly fractionated layered mafic–ultramafic intrusions, a well-known example being the Pd/Au reef in the Upper Middle Zone of the Skaergaard intrusion. Processes proposed to explain why these sulfides are so unusually rich in Cu include fractional crystallization of Fe/(Ni) monosulfide and infiltration of postmagmatic Cu-rich fluids. In this contribution, we explore and experimentally evaluate a third possibility: that Cu-rich magmatic sulfides may be the result of magmatic oxidation. FeS-dominated Ni/Cu-bearing sulfides were equilibrated at variable oxygen fugacities in both open and closed system. Our results show that the Cu/Fe ratio of the sulfide melt increases as a function of oxygen fugacity due to the preferential conversion of FeS into FeO and FeO_1.5, and the resistance of Cu₂S to being converted into an oxide component even at oxygen fugacities characteristic of the sulfide/sulfate transition (above FMQ?+?1). This phenomenon will lead to an increase in the metal/S ratio of a sulfide liquid and will also depress its liquidus temperature. As such, any modeling of the sulfide liquid line of descent in magmatic sulfide complexes needs to address this issue.  相似文献   

Heavy metal accumulation in mangrove sediments surrounding a large waste reservoir of a local metallurgical plant, Sepetiba Bay, SE, Brazil     

E. F. Fonseca  J. A. Baptista Neto  C. G. Silva 《Environmental Earth Sciences》2013,70(2):643-650

Due to the growing rate of urbanization and a rapid and unplanned development in many tropical coastal areas, there continues to be an increasing concern in relation to the impact of anthropogenic activities on mangrove sediments. In southeastern Brazil, the Sepetiba Bay becomes an example of an ecosystem in the process of accelerated degradation. Previous studies highlighted the activities related with zinc processing by an industry on the Madeira’s Island as one of the main source of heavy metal to Sepetiba Bay. Despite the end of the industrial activities in the area, the waste reservoir became the main source of pollutant to the surrounding area. Analyses of Cd, Pb, Cu, Cr, Hg, Ni, Zn, particle size and nutrients of 20 sediment samples collected in the mangrove of the Madeira Island showed that the waste reservoir is the main source of contaminant to the mangrove. The statistic analyses showed that the moisture content and organic matter play an important role in the geochemical dynamic of heavy metal in the area.  相似文献   

Transition zone structure under a stationary hot spot: Cape Verde     

George Helffrich  Bruno Faria  João F.B.D. Fonseca  Alexandra Lodge  Satoshi Kaneshima 《Earth and Planetary Science Letters》2010,289(1-2):156-161

We report on a two-year seismic deployment in the Cape Verde Islands, one goal of which was to study the upper mantle to determine its structure under a hot spot that is stationary in the hot spot reference frame. We find from analysis of P-to-S receiver functions estimated from broadband seismic recordings that, within uncertainty, the time separation between the 410 and 660 km discontinuities is normal compared to radial earth models. Thus, to exist, even stationary hot spots do not require vertical thermal anomalies from deep melting sources anchored in the lower mantle or at the core–mantle boundary or their anomalies are narrower than ～ 250 km in the upper mantle.  相似文献   

Mineralogy and geochemistry of trace metals and REE in volcanic massive sulfide host rocks,stream sediments,stream waters and acid mine drainage from the Lousal mine area (Iberian Pyrite Belt,Portugal)     

E. Ferreira da Silva  I. Bobos  J. Xavier Matos  C. Patinha  A.P. Reis  E. Cardoso Fonseca 《Applied Geochemistry》2009

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Mechanics of thick-skinned Variscan overprinting of Cadomian basement (Iberian Variscides)     

António Ribeiro  José Munhá  António Mateus  Paulo Fonseca  Eurico Pereira  Fernando Noronha  José Romão  José Rodrigues  Paulo Castro  Carlos Meireles  Narciso Ferreira 《Comptes Rendus Geoscience》2009,341(2-3):127-139

Remnants of the Cadomian basement can be found in the Iberian Variscides (IBVA) in several key sectors of its autochthonous units (composed of Neoproterozoic to Lower Palaeozoic metasedimentary sequences) and within the Continental Allochthonous Terrane (CAT). Comprehensive characterization of these critical exposures shows that the prevailing features are related to major geological events dated within the age range of 620–540 Ma. Indeed, near the Cambrian–Ordovician boundary, the IBVA Internal Zones experienced pervasive basement thinning and cover thickening, reflecting diffusive displacement of intracratonic rifting that continued until Lower Devonian times. In the thick-skinned Internal Zones, Helvetic/Penninic style nappes were generated, whereas flower upright axial structures developed along transpressive, intraplate shear zones. These features contrast with those preserved in the thin-skinned IBVA External Zones, dominated by décollements above (un-)deformed Palaeozoic and Cadomian basement. The inferred attenuation of rheological contrast between Cadomian basement and Palaeozoic cover can be explained by inherited fabrics due to thermal softening operated during the Cambrian–Lower Devonian extensional regime. Deeper décollements (and subsequent strain partitioning) are also expected to develop at the upper-lower crust (and at the Moho?) transition, as imaged by the available seismic profiling and MT surveys. The whole data implies a significant discontinuity between Cadomian and Variscan Cycles that should have constrained subsequent lithospheric evolution.  相似文献   

Competing effects of crystal chemistry and silicate melt composition on trace element behavior in magmatic systems: insights from crystal/silicate melt partitioning of the REE,HFSE, Sn,In, Ga,Ba, Pt and Rh     

L.?T.?MichelyEmail author  F.?P.?Leitzke  I.?M.?Speelmanns  R.?O.?C.?Fonseca 《Contributions to Mineralogy and Petrology》2017,172(6):39

We present new partition coefficients for the REE, HFSE, Sn, In, Ga, Ba, Pt and Rh between clinopyroxene, olivine and basaltic melt as a function of crystal chemistry and melt composition at temperatures of 1190–1300 °C and 1-bar pressure. Two components, namely \(\mathrm {Al_2O_3}\) and \(\mathrm {Na_2O}\), were chosen to be investigated since they are known to affect the structure of silicate melts and especially clinopyroxene crystal chemistry. The amount of \(^{[4]}\mathrm{Al}\) in clinopyroxene will result in an increase of \(D_i^\mathrm{{cpx/melt}}\) even after applying a correction factor to account for the effect of melt polymerization. Moreover, the positive correlation between \(^{[4]}\mathrm{Al}\) and \(D_i^\mathrm{{cpx/melt}}\) is not restricted to the REE, but also applies for Sn, Ga, In, and Ba. The addition of up to 2.6 wt% \(\mathrm {Na_2O}\) to the silicate melt universally increases the \(D_i^\mathrm{{cpx/melt}}\) without any concomitant change in crystal chemistry or a significant effect in melt polymerization. This compositional effect is likely due to the ability of Na to break REE–Al complexes in the melt. Our results emphasize the importance of considering all variables that affect the behavior of trace elements in magmatic systems before applying the lattice strain model and derive meaningful results for the changes in the parameters of the crystallographic sites.  相似文献   

The great sulfur depletion of Earth’s mantle is not a signature of mantle–core equilibration     

Chris?BallhausEmail author  Raúl?O.?C.?Fonseca  Carsten?Münker  Arno?Rohrbach  Thorsten?Nagel  Iris?M.?Speelmanns  Hassan?M.?Helmy  Aurelia?Zirner  Antje?K.?Vogel  Alexander?Heuser 《Contributions to Mineralogy and Petrology》2017,172(8):68

The extreme depletion of the Earth’s mantle in sulfur is commonly seen as a signature of metal segregation from Earth’s mantle to Earth’s core. However, in addition to S, the mantle contains other elements as volatile as S that are hardly depleted relative to the lithophile volatility trend although they are potentially as siderophile as sulfur. We report experiments in metal-sulfide–silicate systems to show that the CI normalized abundances of S, Pb, and Sn in Earth’s mantle cannot be reproduced by element partitioning in Fe ± S–silicate systems, neither at low nor at high pressure. Much of the volatile inventory of the Earth’s mantle must have been added late in the accretion history, when metal melt segregation to the core had become largely inactive. The great depletion in S is attributed to the selective segregation of a late sulfide matte from an oxidized and largely crystalline mantle. Apparently, the volatile abundances of Earth’s mantle are not in redox equilibrium with Earth’s core.  相似文献   

Selective chemical extraction of Cu from selected mineral and soil samples: enhancement of Cu geochemical anomalies in Southern Portugal     

E. Cardoso Fonseca  J. Claudino Cardoso  M. Estela Martins  M. Margarida Vairinho 《Journal of Geochemical Exploration》1992,43(3)

The study described herein concerns the application of selective chemical extractions on metal-bearing minerals and soils to geochemical exploration. Specifically, the study aims at the detection of anomalous soils in the vicinity of two mineralized zones in Southern Portugal.A kinetic study of the selectivity of partial chemical extractions applied to Cu minerals has been carried out in order to establish a systematic procedure (reagents, extraction plateau, etc.) which could be recommended for soils of the two study zones. It is shown that: (1) NH₄ acetate dissolves malachite, azurite and cuprite completely and chrysocolla, conicalcite and atacamite only partially; (2) hydroxylamine hydrochloride dissolves chrysocolla and conicalcite only partially; (3) H₂O₂ dissolves chalcopyrite only partially; (4) NH₄ oxalate (U.V.) dissolves conicalcite and atacamite only partially; (5) mixed-acid attack dissolves residual chalcopyrite, chrysocolla, atacamite and conicalcite.A total of 740 soil samples were collected from the Salgadinho and Tinoca areas. The Cu mineralization in the Salgadinho area is situated in an Upper-Devonian Volcanic-Siliceous Complex. The weathering products of the mineralization are mainly amorphous iron oxides, goethite and hematite. The Cu mineralization in Tinoca area is located in the Arronches-Campo Maior belt, where stratiform Cu mineralization is found. The weathering products of the mineralization are mainly malachite, amorphous iron oxides, goethite and hematite.In order to identify the Cu-bearing phases and the extraction plateau, the −80 mesh fraction of two soil samples was submitted to an extraction procedure using the following reagents in sequence: NH₄ acetate, hydroxylamine hydrochloride, NH₄ oxalate (dark), NH₄ oxalate (U.V.) and finally strong acids.In soils from the Salgadinho and Tinoca areas, the use of NH₄ oxalate (U.V.) in single dissolution which would incorporate those phases dissolved by NH₄ acetate and NH₄ oxalate (dark), gives the broadest anomalous surface and higher contrast for Cu than acid digestion. The analysis of NH₄ oxalate (U.V.) extractions, instead of acid digestion, can thus be recommended for both areas.  相似文献   

Hot-fluid Driven Metasomatism of Samalpatti Carbonatites, South India: Evidence from Petrology, Mineral Chemistry, Trace Elements and Stable Isotope Compositions     

Rajesh K. Srivastava  Anand Mohan  Cesar Fonseca Ferreira Filho 《Gondwana Research》2005,8(1):77-85

The magmatic heritage of carbonatites can be identified on the basis of a combination of geological criteria such as, their mode of occurrence, the nature of associated igneous rocks, the presence of minerals of igneous origin, fenitization, characteristic trace element contents and isotopic composition. Late Proterozoic Samalpatti carbonatites were studied in view of these criteria, and were found to contain metamorphic minerals that normally form under thermal metamorphic conditions and which have unusual chemical compositions. A combination of criteria points clearly to a magmatic origin for these carbonatites. Field relations indicate that the dominant modes of intrusion of carbonatite into the encompassing pyroxenites and syenites include small dykes, veins, or lenses. The igneous nature of these carbonatites has been described elsewhere and chemically they are classified as calico-carbonatites. Currently, very little is known about the metamorphic textures and mineralogy observed in the Samalpatti carbonatites. In this study, several metamorphic minerals are reported including diopside, grossularite, vesuvianite, K-feldspar and wollastonite, and a hornfelsic texture is described. These mineral phases and texture characterize thermal metamorphism under low pressure and high temperature (LP-HT) metamorphic conditions (650°_750°C) or metasomatism aided by hot-fluid advection. The metamorphic nature of minerals reported is also confirmed by electron microprobe study. The Samalpatti carbonatite samples show much lower values of characteristic trace elements (P, Sr, Ba, Zr, Nb, Th, Y and REEs) than average concentrations for magmatic carbonatite. Stable isotopic (d¹³C and d¹⁸O) compositions of Samalpatti carbonatites do not fall in the primary igneous carbonatite (PIC) domain. The petrological and chemical signatures of these carbonatites suggest metasomatism in conjunction with fluid advection. Such a metasomatic process may drastically change the chemistry of the rocks in addition to enrichment of heavier stable isotopes. During this metasomatic process, characteristic elements would be dissolved in the high d¹⁸O fluid, and together with Rayleigh fractionation would contribute to enhanced concentrations of ¹³C and ¹⁸O in Samalpatti carbonatites.  相似文献   

Hydroacoustic detection of volcanic ocean-island earthquakes     

George Helffrich  Sandra I. N. Heleno  Bruno Faria  João F. B. D. Fonseca 《Geophysical Journal International》2006,167(3):1529-1536

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