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1.
Orogenic gold mineralization at the Damang deposit, Ghana, is associated with hydrothermal alteration haloes around gold‐bearing quartz veins, produced by the infiltration of a H2O–CO2–K2O–H2S fluid following regional metamorphism. Alteration assemblages are controlled by the protoliths with sedimentary rocks developing a typical assemblage of muscovite, ankerite and pyrite, while intrusive dolerite bodies contain biotite, ankerite and pyrrhotite, accompanied by the destruction of hornblende. Mineral equilibria modelling was undertaken with the computer program thermocalc , in subsets of the model system MnO–Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–CO2–H2O–TiO2–Fe2O3, to constrain conditions of regional metamorphism and the subsequent gold mineralization event. Metapelites with well‐developed amphibolite facies assemblages reliably constrain peak regional metamorphism at ~595 °C and 5.5 kbar. Observed hydrothermal alteration assemblages associated with gold mineralization in a wide compositional range of lithologies are typically calculated to be stable within P–T–X(CO2) arrays that trend towards lower temperatures and pressures with increasing equilibrium fluid X(CO2). These independent P–T–X(CO2) arrays converge and the region of overlap at ~375–425 °C and 1–2 kbar is taken to represent the conditions of alteration approaching equilibrium with a common infiltrating fluid with an X(CO2) of ~0.7. Fluid‐rock interaction calculations with M–X(CO2) diagrams indicate that the observed alteration assemblages are consistent with the addition of a single fluid phase requiring minimum fluid/rock ratios on the order of 1. 相似文献
2.
The 43 t (1.4 Moz) of gold in the Woodcutters goldfield 50 km north of Kalgoorlie has wide geological significance in terms of gold in Archaean granite, as well as its local commercial and exploration significance. Woodcutters is already one of the largest Archaean gold systems in granite, and is unusual in being so far laterally from the nearest greenstone belt. Gold in the Federal zone, one of the deposits making up the Woodcutters goldfield, is hosted in hornblende‐biotite granodiorite,6 km from the mapped contact with greenstone. In Federal open pit, the granodiorite is coarse‐grained in the northern half, and a fine‐grained granodiorite in the south, with both hosting gold. These two types of granodiorite are rather similar in both mineralogy and geochemistry. There is also a subordinate fine‐grained monzodiorite. The Federal gold mineralisation is in a northwest‐striking, northeast‐dipping (315° strike/60°E dip) shear zone in the Scotia granite. Variation in grainsize of the host rocks might have affected the style of deformation with more brittle fabrics in the coarse‐grained phase and more ductile fabrics prominent in the fine‐grained granodiorite. Hydrothermal alteration is extensively developed around the Federal deposit and is a useful vector towards gold mineralisation. Distal epidote alteration surrounds a proximal muscovite‐biotite alteration zone that contains quartz‐sulfide veins. The alteration shares some of the common alteration characteristics of Archaean greenstone‐hosted gold, but differs in that carbonate‐chlorite alteration is only weakly developed. This difference is readily explained in terms of host‐rock composition and lower concentrations of Fe, Mg and Ca in the granite compared with greenstone. Fluid‐inclusion studies demonstrate that the fluids associated with the hydrothermal alteration at Woodcutters shared the common characteristics of fluids in Archaean greenstone gold, namely low‐salinity and dominant H2O–CO2. Fluid inclusions with moderate salinity were found in one fresh sample away from mineralisation, and are inferred to represent possible magmatic fluid. There is no evidence of a granite‐derived fluid being responsible for gold mineralisation. The granodiorite host rock had cooled, crystallised and had at least started to undergo deformation prior to gold introduction. The distribution of gold mineralisation in the Woodcutters goldfield has the style, shape and orientation comparable with greenstone‐hosted gold deposits in the same region. The northwest trend, the quartz veining and simple pyrite mineralogy are all features common to other greenstone‐hosted gold deposits near Kalgoorlie such as Mt Pleasant. The alteration fluid appears to have penetrated the granite on the scale of many hundreds of metres, causing large‐scale alteration. Woodcutters gold mineralisation resulted from the same metamorphic fluid processes that led to formation of greenstone gold deposits. In this metamorphic model, granitic rocks are predicted to be less‐favourable gold hosts than mafic rocks for two reasons. Granitic rocks do not generally fracture during regional deformation in such a way as to create large‐scale dilation. Furthermore, with less iron and no carbon, granitic rocks have lower potential to precipitate gold from solution by wall‐rock reaction. The metamorphic model predicts that those granite types with higher Fe should host better gold deposits, all other factors being equal. Accordingly, tonalite‐trondhjemite and hornblende‐bearing granodiorite should provide better environments for major gold deposits compared with monzogranite, and granite sensu stricto, as borne out by Woodcutters, but mafic rocks should be better hosts than any of these felsic to intermediate rocks. 相似文献
3.
The Holland and Powell internally consistent data set version 5.5 has been augmented to include pyrite, troilite, trov (Fe0.875S), anhydrite, H2S, elemental S and S2 gas. Phase changes in troilite and pyrrhotite are modelled with a combination of multiple end‐members and a Landau tricritical model. Pyrrhotite is modelled as a solid solution between hypothetical end‐member troilite (trot) and Fe0.875S (trov); observed activity–composition relationships fit well to a symmetric formalism model with a value for wtrot?trov of ?3.19 kJ mol?1. The hypothetical end‐member approach is required to compensate for iron distribution irregularities in compositions close to troilite. Mixing in fluids is described with the van Laar asymmetric formalism model with aij values for H2O–H2S, H2S–CH4 and H2S–CO2 of 6.5, 4.15 and 0.045 kJ mol?1 respectively. The derived data set is statistically acceptable and replicates the input data and data from experiments that were not included in the initial regression. The new data set is applied to the construction of pseudosections for the bulk composition of mafic greenschist facies rocks from the Golden Mile, Kalgoorlie, Western Australia. The sequence of mineral assemblages is replicated successfully, with observed assemblages predicted to be stable at X(CO2) increasing with increasing degree of hydrothermal alteration. Results are compatible with those of previous work. Assemblages are insensitive to the S bulk content at S contents of less than 1 wt%, which means that volatilization of S‐bearing fluids and sulphidation are unlikely to have had major effects on the stable mineral assemblage in less metasomatized rocks. The sequence of sulphide and oxide phases is predicted successfully and there is potential to use these phases qualitatively for geobarometry. Increases in X(CO2) stabilized, in turn, pyrite–magnetite, pyrite–hematite and anhydrite–pyrite. Magnetite–pyrrhotite is predicted at temperatures greater than 410 °C. The prediction of a variety of sulphide and oxide phases in a rock of fixed bulk composition as a function of changes in fluid composition and temperature is of particular interest because it has been proposed that such a variation in phase assemblage is produced by the infiltration of multiple fluids with contrasting redox state. The work presented here shows that this need not be the case. 相似文献
4.
《Ore Geology Reviews》2008,33(3-4):629-650
In the Raposos orogenic gold deposit, hosted by banded iron-formation (BIF) of the Archean Rio das Velhas greenstone belt, the hanging wall rocks to BIF are hydrothermally-altered ultramafic schists, whereas metamafic rocks and their hydrothermal schistose products represent the footwall. Planar and linear structures at the Raposos deposit define three ductile to brittle deformational events (D1, D2 and D3). A fourth group of structures involve spaced cleavages that are considered to be a brittle phase of D3. The orebodies constitute sulfide-bearing D1-related shear zones of BIF in association with quartz veins, and result from the sulfidation of magnetite and/or siderite. Pyrrhotite is the main sulfide mineral, followed by lesser arsenopyrite and pyrite. At level 28, the hydrothermal alteration of the mafic and ultramafic wall rocks enveloping BIF define a gross zonal pattern surrounding the ore zones. Metabasalt comprises albite, epidote, actinolite and lesser Mg/Fe–chlorite, calcite and quartz. The incipient stage includes the chlorite and chlorite-muscovite alteration zone. The least-altered ultramafic schist contains Cr-bearing Mg-chlorite, actinolite and talc, with subordinate calcite. The incipient alteration stage is subdivided into the talc–chlorite and chlorite–carbonate zone. For both mafic and ultramafic wall rocks, the carbonate–albite and carbonate–muscovite zones represent the advanced alteration stage.Rare earth and trace element analyses of metabasalt and its alteration products suggest a tholeiitic protolith for this wall rock. In the case of the ultramafic schists, the precursor may have been peridotitic komatiite. The Eu anomaly of the Raposos BIF suggests that it was formed proximal to an exhalative hydrothermal source on the ocean floor. The ore fluid composition is inferred by hydrothermal alteration reactions, indicating it to having been H2O-rich containing CO2 + Na+ and S. Since the distal alteration halos are dominated by hydrated silicate phases (mainly chlorite), with minor carbonates, fixation of H2O is indicated. The CO2 is consumed to form carbonates in the intermediate alteration stage, in halos around the chlorite-dominated zones. These characteristics suggest variations in the H2O to CO2-ratio of the sulfur-bearing, aqueous-carbonic ore fluid, which interacted at varying fluid to rock ratios with progression of the hydrothermal alteration. 相似文献
5.
In the Raposos orogenic gold deposit, hosted by banded iron-formation (BIF) of the Archean Rio das Velhas greenstone belt, the hanging wall rocks to BIF are hydrothermally-altered ultramafic schists, whereas metamafic rocks and their hydrothermal schistose products represent the footwall. Planar and linear structures at the Raposos deposit define three ductile to brittle deformational events (D1, D2 and D3). A fourth group of structures involve spaced cleavages that are considered to be a brittle phase of D3. The orebodies constitute sulfide-bearing D1-related shear zones of BIF in association with quartz veins, and result from the sulfidation of magnetite and/or siderite. Pyrrhotite is the main sulfide mineral, followed by lesser arsenopyrite and pyrite. At level 28, the hydrothermal alteration of the mafic and ultramafic wall rocks enveloping BIF define a gross zonal pattern surrounding the ore zones. Metabasalt comprises albite, epidote, actinolite and lesser Mg/Fe–chlorite, calcite and quartz. The incipient stage includes the chlorite and chlorite-muscovite alteration zone. The least-altered ultramafic schist contains Cr-bearing Mg-chlorite, actinolite and talc, with subordinate calcite. The incipient alteration stage is subdivided into the talc–chlorite and chlorite–carbonate zone. For both mafic and ultramafic wall rocks, the carbonate–albite and carbonate–muscovite zones represent the advanced alteration stage.Rare earth and trace element analyses of metabasalt and its alteration products suggest a tholeiitic protolith for this wall rock. In the case of the ultramafic schists, the precursor may have been peridotitic komatiite. The Eu anomaly of the Raposos BIF suggests that it was formed proximal to an exhalative hydrothermal source on the ocean floor. The ore fluid composition is inferred by hydrothermal alteration reactions, indicating it to having been H2O-rich containing CO2 + Na+ and S. Since the distal alteration halos are dominated by hydrated silicate phases (mainly chlorite), with minor carbonates, fixation of H2O is indicated. The CO2 is consumed to form carbonates in the intermediate alteration stage, in halos around the chlorite-dominated zones. These characteristics suggest variations in the H2O to CO2-ratio of the sulfur-bearing, aqueous-carbonic ore fluid, which interacted at varying fluid to rock ratios with progression of the hydrothermal alteration. 相似文献
6.
Abstract Metapelites in the Altavista area, southwest Virginia Piedmont, USA, underwent allochemical hydrothermal retrograde metamorphism in synmetamorphic shear zones. The metapelites of the Evington Group were metamorphosed in a prograde sequence of chlorite, staurolite, and sillimanite zones. Garnet–biotite geothermometry and phase relations support eastward increasing metamorphic grade, ranging from 570° C in the staurolite zone to 650° C in the sillimanite zone at c. 5.8 kbar. Sillimanite-zone rocks later underwent progressive retrogression around shear zones which acted as fluid conduits. Retrograde assemblages are successively zoned around the shear zones with staurolite-, chloritoid- and kyanite-bearing assemblages. The shear zones commonly contain kyanite or tourmaline veins. Applicable phase equilibria indicate that retrogression occurred during isobaric cooling through c. 200–270° C. Rock compositional changes with retrogression occurred in steps: SiO2 was gained in the early stages of the retrogression but lost in the late stages; Al2O3, K2O, and H2O were increasingly gained through the sequence; CaO was increasingly lost. Addition of H2O and decreasing temperatures resulted in new ferromagnesian minerals (staurolite, chloritoid, chlorite) and changes in H2O, SiO2, Al2O3, K2O, and CaO contents produced muscovite and sodic plagioclase. Subsequent to prograde metamorphism, deeply derived fluids migrated upwards along shear zones, providing fluid and energy for the retrograde reactions. The sheared rocks underwent fluid infiltration with fluid fluxes of 1.8 × 107–4.3 × 107 cm3/cm2 corresponding to minimum estimated fluid-to-rock ratios of 7.5–21 as a function of position within the shear zone. Fluid flow was from high to low temperature early and low to high temperature later in the retrogression. 相似文献
7.
The production of large volumes of fluid from metabasic rocks, particularly in greenstone terranes heated across the greenschist–amphibolite facies transition, is widely accepted yet poorly characterized. The presence of carbonate minerals in such rocks, commonly as a consequence of sea‐floor alteration, has a strong influence, via fluid‐rock buffering, on the mineral equilibria evolution and fluid composition. Mineral equilibria modelling of metabasic rocks in the system Na2O‐CaO‐FeO‐MgO‐Al2O3‐SiO2‐CO2‐H2O (NCaFMASCH) is used to constrain the stability of common metabasic assemblages. Calculated buffering paths on T–XCO2 pseudosections, illustrate the evolution of greenstone terranes during heating across the greenschist‐amphibolite transition. The calculated paths constrain the volume and the composition of fluid produced by devolatilization and buffering. The calculated amount and composition of fluid produced are shown to vary depending on P–T conditions, the proportion of carbonate minerals and the XCO2 of the rocks prior to prograde metamorphism. In rocks with an initially low proportion of carbonate minerals, the greenschist to amphibolite facies transition is the primary period of fluid production, producing fluid with a low XCO2. Rocks with greater initial proportions of carbonate minerals experience a second fluid production event at temperatures above the greenschist to amphibolite facies transition, producing a more CO2‐rich fluid (XCO2 = 0.2–0.3). Rocks may achieve these higher proportions of carbonate minerals either via more extensive seafloor alteration or via infiltration of fluids. Fluid produced via devolatilization of rocks at deeper crustal levels may infiltrate and react with overlying lower temperature rocks, resulting in external buffering of those rocks to higher XCO2 and proportions of carbonate minerals. Subsequent heating and devolatilization of these overlying rocks results in buffering paths that produce large proportions of fluid at XCO2 = 0.2–0.3. The production of fluid of this composition is of importance to models of gold transport in Archean greenstone gold deposits occurring within extensive fluid alteration haloes, as these haloes represent the influx of fluid of XCO2 = 0.2–0.3 into the upper crust. 相似文献
8.
Hydration reactions are direct evidence of fluid–rock interaction during regional metamorphism. In this study, hydration reactions to produce retrograde actinolite in mafic schists are investigated to evaluate the controlling factors on the reaction progress. Mafic schists in the Sanbagawa belt contain amphibole coexisting with epidote, chlorite, plagioclase and quartz. Amphibole typically shows two types of compositional zoning from core to rim: barroisite → hornblende → actinolite in the high‐grade zone, and winchite → actinolite in the low‐grade zone. Both types indicate that amphibole grew during the exhumation stage of the metamorphic belt. Microstructures of amphibole zoning and mass‐balance relations suggest that: (1) the actinolite‐forming reactions proceeded at the expense of the preexisting amphibole; and (2) the breakdown reaction of hornblende consumed more H2O fluid than that of winchite, when one mole of preexisting amphibole was reacted. Reaction progress is indicated by the volume fraction of actinolite to total amphibole, Yact, with the following details: (1) reaction proceeded homogeneously in each mafic layer; (2) the extent of the hornblende breakdown reaction is commonly low (Yact < 0.5), but it increases drastically in the high‐grade part of the garnet zone (Yact > 0.7); and (3) the extent of the winchite breakdown reaction is commonly high (Yact > 0.7). Many microcracks are observed within hornblende, and the extent of hornblende breakdown reaction is correlated with the size reduction of the hornblende core. Brittle fracturing of hornblende may have enhanced retrograde reaction progress by increasing of influx of H2O and the surface area of hornblende. In contrast to high‐grade rocks, the winchite breakdown reaction is well advanced in the low‐grade rocks, where reaction progress is not associated with brittle fracturing of winchite. The high extent of the reaction in the low‐grade rocks may be due to small size of winchite before the reaction. 相似文献
9.
Characteristic Features of REE and Pb–Zn–Ag Mineralizations in the Na Son Deposit,Northeastern Vietnam
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Can Pham‐Ngoc Daizo Ishiyama Tuan Anh Tran Mihoko Hoshino Sachihiro Taguchi 《Resource Geology》2016,66(4):404-418
The Na Son deposit is a small‐scale Pb–ZnPb–Zn–Ag deposit in northeast Vietnam and consists of biotite–chlorite schist, reddish altered rocks, quartz veins and syenite. The biotite–chlorite schist is intruded by syenite. Reddish altered rocks occur as an alteration halo between the biotite–allanite‐bearing quartz veins and the biotite–chlorite schist. Allanite occurs in the biotite–allanite‐bearing quartz veins and in the proximal reddish altered rocks. Rare earth element (REE) fluorocarbonate minerals occur along fractures or at rim of allanite crystals. The later horizontal aggregates of sulfide veins and veinlets cut the earlier reddish altered rocks. The earlier Pb–Zn veins consist of a large amount of galena and lesser amounts of sphalerite, pyrite and molybdenite. The later Cu veins cutting the Pb–Zn veins include chalcopyrite and lesser amounts of tetrahedrite and pyrite. The occurrences of two‐phase H2O–CO2 fluid inclusions in quartz from biotite–allanite‐bearing quartz veins and REE‐bearing fluorocarbonate minerals in allanite suggest the presence of CO2 and F in the hydrothermal fluid. The oxygen isotopic ratios of the reddish altered rocks, biotite–chlorite schist, and syenite range from +13.9 to +14.9 ‰, +11.5 to +13.3 ‰, and +10.1 to +11.6 ‰, respectively. Assuming an isotopic equilibrium between quartz (+14.6 to +15.8 ‰) and biotite (+8.6 ‰) in the biotite–allanite‐bearing quartz vein, formation temperature was estimated to be 400°C. At 400°C, δ18O values of the hydrothermal fluid in equilibrium with quartz and biotite range from +10.5 to +11.7 ‰. These δ18O values are consistent with fluid that is derived from metamorphism. Assuming an isotopic equilibrium between galena (+1.5 to +1.7 ‰) and chalcopyrite (+3.4 ‰), the formation temperature was estimated to be approximately 300°C. The formation temperature of the Na Son deposit decreased with the progress of mineralization. Based on the geological data, occurrence of REE‐bearing minerals and oxygen isotopic ratios, the REE mineralization is thought to result from interaction between biotite–chlorite schist and REE‐, CO2‐ and F‐bearing metamorphic fluid at 400°C under a rock‐dominant condition. 相似文献
10.
P. A. Polito Y. Bone J. D. A. Clarke T. P. Mernagh 《Australian Journal of Earth Sciences》2013,60(6):833-855
The Junction gold deposit, in Western Australia, is an orogenic gold deposit hosted by a differentiated, iron‐rich, tholeiitic dolerite sill. Petrographic, microthermometric and laser Raman microprobe analyses of fluid inclusions from the Junction deposit indicate that three different vein systems formed at three distinct periods of geological time, and host four fluid‐inclusion populations with a wide range of compositions in the H2O–CO2–CH4–NaCl ± CaCl2 system. Pre‐shearing, pre‐gold, molybdenite‐bearing quartz veins host fluid inclusions that are characterised by relatively consistent phase ratios comprising H2O–CO2–CH4 ± halite. Microthermometry suggests that these veins precipitated when a highly saline, >340°C fluid mixed with a less saline ≥150°C fluid. The syn‐gold mineralisation event is hosted within the Junction shear zone and is associated with extensive quartz‐calcite ± albite ± chlorite ± pyrrhotite veining. Fluid‐inclusion analyses indicate that gold deposition occurred during the unmixing of a 400°C, moderately saline, H2O–CO2 ± CH4 fluid at pressures between 70 MPa and 440 MPa. Post‐gold quartz‐calcite‐biotite‐pyrrhotite veins occupy normal fault sets that slightly offset the Junction shear zone. Fluid inclusions in these veins are predominantly vapour rich, with CO2?CH4. Homogenisation temperatures indicate that the post‐gold quartz veins precipitated from a 310 ± 30°C fluid. Finally, late secondary fluid inclusions show that a <200°C, highly saline, H2O–CaCl2–NaCl–bearing fluid percolated along microfractures late in the deposit's history, but did not form any notable vein type. Raman spectroscopy supports the microthermometric data and reveals that CH4–bearing fluid inclusions occur in syn‐gold quartz grains found almost exclusively at the vein margin, whereas CO2–bearing fluid inclusions occur in quartz grains that are found toward the centre of the veins. The zonation of CO2:CH4 ratios, with respect to the location of fluid inclusions within the syn‐gold quartz veins, suggest that the CH4 did not travel as part of the auriferous fluid. Fluid unmixing and post‐entrapment alteration of the syn‐gold fluid inclusions are known to have occurred, but cannot adequately account for the relatively ordered zonation of CO2:CH4 ratios. Instead, the late introduction of a CH4–rich fluid into the Junction shear zone appears more likely. Alternatively, the process of CO2 reduction to CH4 is a viable and plausible explanation that fits the available data. The CH4–bearing fluid inclusions occur almost exclusively at the margin of the syn‐gold quartz veins within the zone of high‐grade gold mineralisation because this is where all the criteria needed to reduce CO2 to CH4 were satisfied in the Junction deposit. 相似文献
11.
The H2O and CO2 content of cordierite was analysed in 34 samples from successive contact metamorphic zones of the Etive thermal aureole, Scotland, using Fourier‐transform infrared spectroscopy (FTIR). The measured volatile contents were used to calculate peak metamorphic H2O and CO2 activities. Total volatile contents are compared with recently modelled cordierite volatile saturation surfaces in order to assess the extent of fluid‐present v. fluid‐absent conditions across the thermal aureole. In the middle aureole, prior to the onset of partial melting, calculated aH2O values are high, close to unity, and measured volatile contents intersect modelled H2O–CO2 saturation curves at the temperature of interest, suggesting that fluid‐present conditions prevailed. Total volatile contents and aH2O steadily decrease beyond the onset of partial melting, consistent with the notion of aH2O being buffered to lower values as melting progresses once free hydrous fluid is exhausted. All sillimanite zone samples record total volatile contents that are significantly lower than modelled H2O–CO2 saturation surfaces, implying that fluid‐absent conditions prevailed. The lowest recorded aH2O values lie entirely within part of the section where fluid‐absent melting reactions are thought to have dominated. Samples within 30 m of the igneous contact appear to be re‐saturated, possibly via a magmatically derived fluid. In fluid‐absent parts of the aureole, cordierite H2O contents yield melt–H2O contents that are compatible with independently determined melt–H2O contents. The internally consistent cordierite volatile data and melt–H2O data support the conclusion that the independent P–T estimates applied to the Etive rocks were valid and that measured cordierite volatile contents are representative of peak metamorphic values. The Etive thermal aureole provides the most compelling evidence, suggesting that the cordierite fluid monitor can be used to accurately assess the fluid conditions during metamorphism and partial melting in a thermal aureole. 相似文献
12.
The Mihalıççık region (Eskişehir) in NW Turkey includes an ophiolitic assemblage with a serpentinite‐matrix mélange. The serpentinites of this mélange host silica‐carbonate metasomatites which were previously named as listvenites. Our mineralogical and geochemical studies revealed that these alteration assemblages represent members of the listvenitic series, mainly the carbonate rocks, silica‐carbonate rocks and birbirites, rather than true listvenites (sensu stricto). Tectonic activity and lithology are principal factors that control the formation of these assemblages. Carbonatization and silicification of the serpentinite host‐rock is generated by CO2, SiO2‐rich H2O hydrothermal fluid which includes As, Ba, Sb and Sr. Low precious metal (Au, Ag) contents of the alteration assemblages indicate lack of these metals in the fluid. Primary assemblages of the alteration are carbonate rocks that are followed by silica‐carbonate rocks and birbirites, respectively. Petrographic studies and chemical analyses suggested an alkaline and moderate to high temperature (350–400°C) fluid with low oxygen and sulphur fugacity for the carbonatization of the serpentinites. The low temperature phases observed in the subsequent silicification indicated that the fluid cooled during progressive alteration. The increasing Fe‐oxide content and sulphur phases also suggested increasing oxygen and sulphur fugacity during this secondary process and silica‐carbonate rock formation. The occurrence of birbirites is considered as a result of reactivation of tectonic features. These rocks are classified in two sub‐groups; the Group 1 birbirites show analogous rare earth element (REE) trends with the serpentinite host‐rock, and the Group 2 birbirites simulate the REE trends of the nearby tectonic granitoid slices. The unorthodox REE trend of Group 2 birbirites is interpreted to have resulted from a mobilization process triggered by the weathering solutions rather than being products of enrichment by the higher temperature hydrothermal activity. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
13.
D. A. Holwell G. R. T. Jenkin K. G. Butterworth T. Abraham-James A. J. Boyce 《Mineralium Deposita》2013,48(4):453-466
A gold-bearing quartz vein system has been identified in Archaean basement rocks at Sortekap in the Kangerlussuaq region of east Greenland, 35 km north–northeast of the Skaergaard Intrusion. This constitutes the first recorded occurrence of Au mineralisation in the metamorphic basement rocks of east Greenland. The mineralisation can be classified as orogenic style, quartz vein-hosted Au mineralisation. Two vein types have been identified based on their alteration styles and the presence of Au mineralisation. Mineralised type 1 veins occur within sheared supracrustal units and are hosted by garnet-bearing amphibolites, with associated felsic and ultramafic intrusions. Gold is present as native Au and Au-rich electrum together with arsenopyrite and minor pyrite and chalcopyrite in thin alteration selvages in the immediate wall rocks. The alteration assemblage of actinolite-clinozoisite-muscovite-titanite-scheelite-arsenopyrite-pyrite is considered to be a greenschist facies assemblage. The timing of mineralisation is therefore interpreted as being later and separate event to the peak amphibolite facies metamorphism of the host rocks. Type 2 quartz veins are barren of mineralisation, lack significant alteration of the wall rocks and are considered to be later stage. Fluid inclusion microthermometry of the quartz reveals three separate fluids, including a high temperature (T h ?=?300–350 °C), H2O–CO2–CH4 fluid present only in type 1 veins that in interpreted to be responsible for the main stage of Au deposition and sulphidic wall rock alteration. It is likely that the carbonic fluids were actually trapped at temperatures closer to 400 °C. Two other fluids were identified within both vein types, which comprise low temperature (100–200 °C) brines, with salinities of 13–25 wt%?eq. NaCl and at least one generation of low salinity aqueous fluids. The sources and timings of the secondary fluids are currently equivocal but they may be related to the emplacement of Paleogene mafic intrusions. The identification of this occurrence of orogenic-style Au mineralisation has implications for exploration in the underexplored area of east Greenland between 62 and 69°?N, where other, similar supracrustal units are known to be present. 相似文献
14.
Melting, carbonic fluids and water recycling in the deep crust: an example from the Limpopo Belt, South Africa 总被引:1,自引:0,他引:1
G. STEVENS 《Journal of Metamorphic Geology》1997,15(1):141-154
The proposed retrograde orthoamphibole isograd in the Southern Marginal Zone of the Limpopo Belt separates hydrated, amphibolite grade metapelites from their granulite grade precursors and provides an intriguing geological dilemma. Widespread rehydration of metapelitic granulites under conditions of 660–600 °C and ≥0.6 GPa, and CO2-dominated fluid-inclusion populations appear to suggest thorough flushing of the high-grade crust with an externally derived carbonic fluid. However, past studies of the carbon and oxygen isotope geochemistry of the hydrated rocks have not demonstrated the involvement of any voluminous out of equilibrium’ fluid in the evolution of the rocks. This contribution proposes a model wherein the hydrating fluids are derived from crystallizing anatectic leucosomes, generated by in situ fluid-absent biotite melting along the prograde path. Model equilibrium fluid compositions suggest that reaction between this melt-derived H2O and biogenic graphite produced CO2-rich fluid compositions and potentially high fluid:rock ratios at the wet granite solidus. Declining temperature resulted in fluid compositions shifting to higher XH2O, with the precipitation of graphite essentially at the sites of initial fluid generation, thereby preserving original (pre-metamorphic) isotopic heterogeneities. The hydration pattern of the Southern Marginal Zone appears to be a function of melt migration. In the hydrated zone, leucosomes generally approximate minimum melt compositions and in this zone H2O was effectively recycled between the prograde and retrograde assemblages. In contrast, leucosomes in the granulite grade portion of the terrane have lost a K2O- and H2O-rich melt fraction, and although some hydration has occurred in this zone, orthopyroxene is generally preserved in metapelites. In a general context, in situ crystallization of graphitic partially melted source rocks has the potential to produce high fluid-rock ratios at temperatures close to the wet granite solidus. This single process holds the potential for widespread retrogression of formerly high-grade assemblages, at a variety of aH2O values, without external fluid input. 相似文献
15.
The world-class Natalka gold deposit, northeast Russia: REE patterns, fluid inclusions, stable oxygen isotopes, and formation conditions of ore 总被引:1,自引:0,他引:1
N. A. Goryachev O. V. Vikent’eva N. S. Bortnikov V. Yu. Prokof’ev V. A. Alpatov V. V. Golub 《Geology of Ore Deposits》2008,50(5):362-390
REE patterns of hydrothermally altered rocks, fluid inclusions, and stable oxygen isotopes of quartz were studied at the Natalka gold deposit. Metasomatic rocks formed under decompression reveal gradual depletion in LREE and HREE relative to siltstone of the protolith. The HREE patterns of metasomatic rocks formed under decompression are uniform; an insignificant removal of LREE can be noted. The progressive extraction of REE with increasing alteration of rocks could have been due to the effect of magmatogenic or meteoric fluid. Because a Ce anomaly is absent, the participation of oxidized meteoric water was limited. The inverse correlation between the total REE content and the Eu anomaly value in altered rocks indicates a substantial role of magmatogenic fluid. The REE patterns of altered rocks formed under compression show that the role of metamorphic fluid was not great. All metasomatic rocks are enriched in LREE, so that the enrichment of fluid in LREE as well may be suggested. Three fluid compositions were captured as fluid inclusions: (1) H2O-CO2-NaCl-MgCl2 with a salinity of 1.0–4.9 wt % NaCl equiv, (2) CO2-CH4, and (3) H2O-NaCl-MgCl2 with a salinity of 7.0–5.6 wt % NaCl equiv. Compositions (1) and (2) coexisted in the mineral-forming system at 250–350°C and 1.1–2.4 kbar as products of phase separation under conditions of decreasing P and T. The interaction of this fluid with host rocks resulted in the formation of extensive halos of beresitized rocks with sulfide disseminations. The precipitation of arsenopyrite and pyrite led to the substantial depletion of mineral-forming fluid in H2S and destabilization of the Au(HS)2? complex. The fluid with the third composition arose due to the boiling of the H2O-CO2-CH4-NaCl-MgCl2 liquid and was responsible for metasomatic alteration of host rocks. The late mineral assemblages were deposited from this fluid at the initial stage of ore formation. The high methane concentrations in the ore-forming fluid were likely caused by interaction of hydrothermal ore-bearing solutions with carbonaceous host rocks. The δ18O values of quartz from quartz-scheelite-pyrite-arsenopyrite and sulfide-sulfosalt mineral assemblages vary from +11.6 to +14.1‰ and +11.2 to +13.5‰, respectively. The parental fluids of the early and late mineral assemblages probably were derived from a magmatic source and were characterized by $ \delta ^{18} O_{H_2 O} REE patterns of hydrothermally altered rocks, fluid inclusions, and stable oxygen isotopes of quartz were studied at the Natalka
gold deposit. Metasomatic rocks formed under decompression reveal gradual depletion in LREE and HREE relative to siltstone
of the protolith. The HREE patterns of metasomatic rocks formed under decompression are uniform; an insignificant removal
of LREE can be noted. The progressive extraction of REE with increasing alteration of rocks could have been due to the effect
of magmatogenic or meteoric fluid. Because a Ce anomaly is absent, the participation of oxidized meteoric water was limited.
The inverse correlation between the total REE content and the Eu anomaly value in altered rocks indicates a substantial role
of magmatogenic fluid. The REE patterns of altered rocks formed under compression show that the role of metamorphic fluid
was not great. All metasomatic rocks are enriched in LREE, so that the enrichment of fluid in LREE as well may be suggested.
Three fluid compositions were captured as fluid inclusions: (1) H2O-CO2-NaCl-MgCl2 with a salinity of 1.0–4.9 wt % NaCl equiv, (2) CO2-CH4, and (3) H2O-NaCl-MgCl2 with a salinity of 7.0–5.6 wt % NaCl equiv. Compositions (1) and (2) coexisted in the mineral-forming system at 250–350°C
and 1.1–2.4 kbar as products of phase separation under conditions of decreasing P and T. The interaction of this fluid with host rocks resulted in the formation of extensive halos of beresitized rocks with sulfide
disseminations. The precipitation of arsenopyrite and pyrite led to the substantial depletion of mineral-forming fluid in
H2S and destabilization of the Au(HS)2− complex. The fluid with the third composition arose due to the boiling of the H2O-CO2-CH4-NaCl-MgCl2 liquid and was responsible for metasomatic alteration of host rocks. The late mineral assemblages were deposited from this
fluid at the initial stage of ore formation. The high methane concentrations in the ore-forming fluid were likely caused by
interaction of hydrothermal ore-bearing solutions with carbonaceous host rocks. The δ18O values of quartz from quartz-scheelite-pyrite-arsenopyrite and sulfide-sulfosalt mineral assemblages vary from +11.6 to
+14.1‰ and +11.2 to +13.5‰, respectively. The parental fluids of the early and late mineral assemblages probably were derived
from a magmatic source and were characterized by = +6.3 to +8.8‰ at 350°C and +3.6 to +5.9‰ at 280°C, respectively. The narrow interval of oxygen isotopic compositions shows
that this source was homogeneous. The data obtained allow us to suggest that the deposit formation was related to magmatic
activity, including the direct supply of ore components from a magma chamber and mobilization of these components in the processes
of dehydration and decarbonation during contact and regional metamorphism.
Original Russian Text ? N.A. Goryachev, O.V. Vikent’eva, N.S. Bortnikov, V.Yu. Prokof’ev, V.A. Alpatov, V.V. Golub, 2008,
published in Geologiya Rudnykh Mestorozhdenii, 2008, Vol. 50, No. 5, pp. 414–444. 相似文献
16.
The stability of pumpellyite + actinolite or riebeckite + epidote + hematite (with chlorite, albite, titanite, quartz and H2O in excess) mineral assemblages in LTMP metabasite rocks is strongly dependent on bulk composition. By using a thermodynamic approach (THERMOCALC), the importance of CaO and Fe2O3 bulk contents on the stability of these phases is illustrated using P–T and P–X phase diagrams. This approach allowed P–T conditions of ~4.0 kbar and ~260 °C to be calculated for the growth of pumpellyite + actinolite or riebeckite + epidote + hematite assemblages in rocks containing variable bulk CaO and Fe2O3 contents. These rocks form part of an accretionary wedge that developed along the east Australian margin during the Carboniferous–Triassic New England Orogen. P–T and P–X diagrams show that sodic amphibole, epidote and hematite will grow at these conditions in Fe2O3‐saturated (6.16 wt%) metabasic rocks, whereas actinolite and pumpellyite will be stable in CaO‐rich (10.30 wt%) rocks. With intermediate Fe2O3 (~3.50 wt%) and CaO (~8.30 wt%) contents, sodic amphibole, actinolite and epidote can coexist at these P–T conditions. For Fe2O3‐saturated rocks, compositional isopleths for sodic amphibole (Al3+ and Fe3+ on the M2 site), epidote (Fe3+/Fe3+ + Al3+) and chlorite (Fe2+/Fe2+ + Mg) were calculated to evaluate the efficiency of these cation exchanges as thermobarometers in LTMP metabasic rocks. Based on these calculations, it is shown that Al3+ in sodic amphibole and epidote is an excellent barometer in chlorite, albite, hematite, quartz and titanite buffered assemblages. The effectiveness of these barometers decreases with the breakdown of albite. In higher‐P stability fields where albite is absent, Fe2+‐Mg ratios in chlorite may be dependent on pressure. The Fe3+/Al and Fe2+/Mg ratios in epidote and chlorite are reliable thermometers in actinolite, epidote, chlorite, albite, quartz, hematite and titanite buffered assemblages. 相似文献
17.
K. Piessens Muchez S. Dewaele A. Boyce W. De Vos M. Sintubin T. N. Debacker E. A. J. Burke W. Viaene 《Tectonophysics》2002,348(1-3)
In the Lower Palaeozoic rocks of the Brabant Massif (Belgium), a recently discovered polysulphide mineralisation is related to a low-angle reverse shear zone. This shear zone has been attributed to the main early Devonian deformation event. Data from boreholes and outcrops allow a detailed investigation of the alteration pattern and palaeofluid flow along this shear zone. Macroscopic observations of the mineralogy and quantitative changes in the phyllosilicate mineralogy indicate that this shear zone is characterised by an envelope of intense sericitisation and silicification. In addition, chloritisation is associated with this alteration. The alteration zone may reach a thickness of 250 m. Ore mineralisation occurred synkinematically and is spatially related to the shear zone. The mineralisation consists of pyrite, marcasite, arsenopyrite, pyrrhotite, chalcopyrite, sphalerite, galena, stibnite and smaller amounts of tetrahedrite and other sulphosalts. It is concentrated in quartz–sulphide veins or occurs diffusely in the host rock. The mineralising fluids have a low-salinity H2O–CO2–CH4–NaCl–(KCl) composition and a minimum temperature of 250–320 °C. The δ18O values of quartz vary between +12.3‰ and +14.5‰ SMOW, and δD compositions of the fluid inclusions in the quartz crystals range from −65‰ to −35‰ V-SMOW. The δD and the calculated δ18O values of the mineralising fluids fall in the range typical for metamorphic fluids and partly overlap with that for primary magmatic fluids. The δ34S values, between +4.7‰ and +10.6‰ CDT, fall outside the interval typical for I-type magmas. Important migration of likely metamorphic fluids, causing a widespread alteration and a polysulphide mineralisation along a low-angle shear zone, has, thus, been identified for the first time in the Caledonian Anglo-Brabant fold belt. 相似文献
18.
Manuel D. Menzel Carlos J. Garrido Vicente Lpez Snchez‐Vizcaíno Kroly Hidas Claudio Marchesi 《Journal of Metamorphic Geology》2019,37(5):681-715
At sub‐arc depths, the release of carbon from subducting slab lithologies is mostly controlled by fluid released by devolatilization reactions such as dehydration of antigorite (Atg‐) serpentinite to prograde peridotite. Here we investigate carbonate–silicate rocks hosted in Atg‐serpentinite and prograde chlorite (Chl‐) harzburgite in the Milagrosa and Almirez ultramafic massifs of the palaeo‐subducted Nevado‐Filábride Complex (NFC, Betic Cordillera, S. Spain). These massifs provide a unique opportunity to study the stability of carbonate during subduction metamorphism at P–T conditions before and after the dehydration of Atg‐serpentinite in a warm subduction setting. In the Milagrosa massif, carbonate–silicate rocks occur as lenses of Ti‐clinohumite–diopside–calcite marbles, diopside–dolomite marbles and antigorite–diopside–dolomite rocks hosted in clinopyroxene‐bearing Atg‐serpentinite. In Almirez, carbonate–silicate rocks are hosted in Chl‐harzburgite and show a high‐grade assemblage composed of olivine, Ti‐clinohumite, diopside, chlorite, dolomite, calcite, Cr‐bearing magnetite, pentlandite and rare aragonite inclusions. These NFC carbonate–silicate rocks have variable CaO and CO2 contents at nearly constant Mg/Si ratio and high Ni and Cr contents, indicating that their protoliths were variable mixtures of serpentine and Ca‐carbonate (i.e., ophicarbonates). Thermodynamic modelling shows that the carbonate–silicate rocks attained peak metamorphic conditions similar to those of their host serpentinite (Milagrosa massif; 550–600°C and 1.0–1.4 GPa) and Chl‐harzburgite (Almirez massif; 1.7–1.9 GPa and 680°C). Microstructures, mineral chemistry and phase relations indicate that the hybrid carbonate–silicate bulk rock compositions formed before prograde metamorphism, likely during seawater hydrothermal alteration, and subsequently underwent subduction metamorphism. In the CaO–MgO–SiO2 ternary, these processes resulted in a compositional variability of NFC serpentinite‐hosted carbonate–silicate rocks along the serpentine‐calcite mixing trend, similar to that observed in serpentinite‐hosted carbonate‐rocks in other palaeo‐subducted metamorphic terranes. Thermodynamic modelling using classical models of binary H2O–CO2 fluids shows that the compositional variability along this binary determines the temperature of the main devolatilization reactions, the fluid composition and the mineral assemblages of reaction products during prograde subduction metamorphism. Thermodynamic modelling considering electrolytic fluids reveals that H2O and molecular CO2 are the main fluid species and charged carbon‐bearing species occur only in minor amounts in equilibrium with carbonate–silicate rocks in warm subduction settings. Consequently, accounting for electrolytic fluids at these conditions slightly increases the solubility of carbon in the fluids compared with predictions by classical binary H2O–CO2 fluids, but does not affect the topology of phase relations in serpentinite‐hosted carbonate‐rocks. Phase relations, mineral composition and assemblages of Milagrosa and Almirez (meta)‐serpentinite‐hosted carbonate–silicate rocks are consistent with local equilibrium between an infiltrating fluid and the bulk rock composition and indicate a limited role of infiltration‐driven decarbonation. Our study shows natural evidence for the preservation of carbonates in serpentinite‐hosted carbonate–silicate rocks beyond the Atg‐serpentinite breakdown at sub‐arc depths, demonstrating that carbon can be recycled into the deep mantle. 相似文献
19.
《Ore Geology Reviews》2009,35(4):580-596
The Semna gold deposit is one of several vein-type gold occurrences in the central Eastern Desert of Egypt, where gold-bearing quartz veins are confined to shear zones close to the boundaries of small granitoid stocks. The Semna gold deposit is related to a series of sub-parallel quartz veins along steeply dipping WNW-trending shear zones, which cut through tectonized metagabbro and granodiorite rocks. The orebodies exhibit a complex structure of massive and brecciated quartz consistent with a change of the paleostress field from tensional to simple shear regimes along the pre-existing fault segments. Textural, structural and mineralogical evidence, including open space structures, quartz stockwork and alteration assemblages, constrain on vein development during an active fault system. The ore mineral assemblage includes pyrite, chalcopyrite, subordinate arsenopyrite, galena, sphalerite and gold. Hydrothermal chlorite, carbonate, pyrite, chalcopyrite and kaolinite are dominant in the altered metaggabro; whereas, quartz, sericite, pyrite, kaolinite and alunite characterize the granodiorite rocks in the alteration zones. Mixtures of alunite, vuggy silica and disseminated sulfides occupy the interstitial open spaces, common at fracture intersections. Partial recrystallization has rendered the brecciation and open space textures suggesting that the auriferous quartz veins were formed at moderately shallow depths in the transition zone between mesothermal and epithermal veins.Petrographic and microthermometric studies aided recognition of CO2-rich, H2O-rich and mixed H2O–CO2 fluid inclusions in the gold-bearing quartz veins. The H2O–CO2 inclusions are dominant over the other two types and are characterized by variable vapor: liquid ratios. These inclusions are interpreted as products of partial mixing of two immiscible carbonic and aqueous fluids. The generally light δ34S of pyrite and chalcopyrite may suggest a magmatic source of sulfur. Spread in the final homogenization temperatures and bulk inclusion densities are likely due to trapping under pressure fluctuation through repeated fracture opening and sealing. Conditions of gold deposition are estimated on basis of the fluid inclusions and sulfur isotope data as 226–267 °C and 350–1100 bar, under conditions transitional between mesothermal and epithermal systems.The Semna gold deposit can be attributed to interplay of protracted volcanic activity (Dokhan Volcanics?), fluid mixing, wallrock sulfidation and a structural setting favoring gold deposition. Gold was transported as Au-bisulfide complexes under weak acid conditions concomitant with quartz–sericite–pyrite alteration, and precipitated through a decrease in gold solubility due to fluid cooling, mixing with meteoric waters and variations in pH and fO2. 相似文献
20.
Previous models of hydrodynamics in contact metamorphic aureoles assumed flow of aqueous fluids, whereas CO2 and other species are also common fluid components in contact metamorphic aureoles. We investigated flow of mixed CO2–H2O fluid and kinetically controlled progress of calc‐silicate reactions using a two‐dimensional, finite‐element model constrained by the geological relations in the Notch Peak aureole, Utah. Results show that CO2 strongly affects fluid‐flow patterns in contact aureoles. Infiltration of magmatic water into a homogeneous aureole containing CO2–H2O sedimentary fluid facilitates upward, thermally driven flow in the inner aureole and causes downward flow of the relatively dense CO2‐poor fluid in the outer aureole. Metamorphic CO2‐rich fluid tends to promote upward flow in the inner aureole and the progress of devolatilization reactions causes local fluid expulsion at reacting fronts. We also tracked the temporal evolution of P‐T‐XCO2conditions of calc‐silicate reactions. The progress of low‐ to medium‐grade (phlogopite‐ to diopside‐forming) reactions is mainly driven by heat as the CO2 concentration and fluid pressure and temperature increase simultaneously. In contrast, the progress of the high‐grade wollastonite‐forming reaction is mainly driven by infiltration of chemically out‐of‐equilibrium, CO2‐poor fluid during late‐stage heating and early cooling of the inner aureole and thus it is significantly enhanced when magmatic water is involved. CO2‐rich fluid dominates in the inner aureole during early heating, whereas CO2‐poor fluid prevails at or after peak temperature is reached. Low‐grade metamorphic rocks are predicted to record the presence of CO2‐rich fluid, and high‐grade rocks reflect the presence of CO2‐poor fluid, consistent with geological observations in many calc‐silicate aureoles. The distribution of mineral assemblages predicted by our model matches those observed in the Notch Peak aureole. 相似文献