Fluid Chemistry

Multi-element crush-leach analysis of H2O-CO2 inclusion fluids from a suite of six vein samples from gold-quartz veins in the Brusson district demonstrates that their solute chemistry (c. 5 wt.% NaCl equivalent) is dominated by sodium chloride with lesser amounts of calcium bicarbonate, potassium chloride and sodium bicarbonate. The samples have been analysed both for gas species (CO2, H2O, N2 and H2S) and for Na, K, Li, Rb, Ca, Mg, Sr, Ba, Fe, Mn, Zn, Pb, Cu, Al, As, B, SO42−, F, Cl, Br and I. The fluids contain appreciable H2S (>10−3 molal), which correlates with the contents of As, CO2 and B. Concentrations of many cations remain similar irrespective of wall rock, but there is evidence of leaching of Li, and possibly I, from some wall rocks. Large variations in the K-content of the fluid may result from precipitation of sericite. The bicarbonate concentrations in the fluids, estimated from charge imbalance, are substantially less than their total CO2 content when trapped as si...

A detailed geochemical study of fluids from representative quartz-sealed faults hosting late Hercynian gold concentrations shows that fluids percolating the mineralised faults had two main distinct reservoirs: one was a quite shallow and the other rather deep-seated. Both fluids have lost a great part of their original geochemical signature through interactions with host metamorphic formations. Early fluids, present during the primary sealing of the faults by quartz, are considered to have effectively equilibrated with the metamorphic pile and then predominantly flowed upwards along the faults. They are characterised by CH 4 /CO 2 /H 2 O ratios rather typical of fluids equilibrated with graphite, and moderate to medium chlorinities with a high Br/Cl ratio. The striking feature of the gold-bearing quartz is that gold is not synchronous within any quartz deposition, and appears located in late microfractures and associated with Pb -Bi -Sb sulphosalts and sulphides. These late stages are characterised by fluids whose salinities decrease to very low values indicating their progressive dilution by waters of more surficial origin in the fault system. The long-lived activity of the fault favoured the connection between two distinct fluid reservoirs at a critical time during the basement uplift. The fluids evolved through two main driving mechanisms which were responsible for the Au deposition: (i) decrease in temperature accompanying decompression from supra-lithostatic to hydrostatic conditions which yielded, in some instances, volatile unmixing in the faulted systems, (ii) mixing of the resulting fluids with waters entering the hydrological systems from shallower reservoirs. In addition to dilution and fluid mixing which are favourable factors for decreasing the gold solubility, the presence of microfractured sulphides could have enhanced gold precipitation through electrochemical processes.

The Palaeoproterozoic Vempalle Formation of the Cuddapah Basin, India, significantly adds to our understanding of the evolution of Precambrian marine carbonate systems and the redox state of the Earth's early oceans. A faciesmicrofacies-diagenetic-geochemical examination of samples from a 900-m long exposure in a freshly-cut canal section shows that 10 to 15 % of precursor limestone is still preserved in the Vempalle Formation in the form of remnant patches of calcimicrite and ooids with calcite spar cement. The ooids, preserving primary radial and concentric fabrics and radial fractures, are considered to have been originally precipitated as calcite, which may have been low-Mg. In places the preserved calcite spar, that is partially replaced by fabric-destructive dolomite, shows Type I calcite twin lamellae. Petrographic observations demonstrate that Vempalle Formation dolomite formed through very early precipitation, which in stromatolites preserved microbial filaments, as well as through fabric-destructive dolomitization during shallow to moderate burial. Vempalle Formation dolomite is characterized by micritic dolomite crystals which suggest rapid early dolomitization of lime mud and micritic calcite from a supersaturated Mg-Ca-rich solution, probably near-surface or during shallow burial. Depletion of Na and Sr contents of Vempalle Formation dolomite along with negative 18O values indicate dolomite recrystallisation during burial and further replacement. Dolomite 13C values of-0.5 to 2 ‰ are likely inherited original marine values. Geochemical proxies (trace elements and rare earths) imply that Cuddapah Basin seawater and dolomitizing fluids were anoxic and ferruginous but not euxinic. Geochemical analyses also indicate that the burial diagenetic fluids evolved from Eu-enriched seawater that probably resulted from continental rifting around 1.9-2.0 Ga. This probable ocean chemistry is in contrast with the anoxic, ferruginous and extremely high Mg/Ca "dolomite oceans" that prevailed during Proterozoic time. The Vempalle dolomite shows more similarities with dolomitised Phanerozoic platform carbonates than typical Precambrian dolomite with its well-preserved textures and burial dolospar cements.

The Palaeoproterozoic Vempalle Formation of the Cuddapah Basin, India, significantly adds to our understanding of the evolution of Precambrian marine carbonate systems and the redox state of the Earth's early oceans. A faciesmicrofacies-diagenetic-geochemical examination of samples from a 900-m long exposure in a freshly-cut canal section shows that 10 to 15 % of precursor limestone is still preserved in the Vempalle Formation in the form of remnant patches of calcimicrite and ooids with calcite spar cement. The ooids, preserving primary radial and concentric fabrics and radial fractures, are considered to have been originally precipitated as calcite, which may have been low-Mg. In places the preserved calcite spar, that is partially replaced by fabric-destructive dolomite, shows Type I calcite twin lamellae. Petrographic observations demonstrate that Vempalle Formation dolomite formed through very early precipitation, which in stromatolites preserved microbial filaments, as well as through fabric-destructive dolomitization during shallow to moderate burial. Vempalle Formation dolomite is characterized by micritic dolomite crystals which suggest rapid early dolomitization of lime mud and micritic calcite from a supersaturated Mg-Ca-rich solution, probably near-surface or during shallow burial. Depletion of Na and Sr contents of Vempalle Formation dolomite along with negative 18O values indicate dolomite recrystallisation during burial and further replacement. Dolomite 13C values of-0.5 to 2 ‰ are likely inherited original marine values. Geochemical proxies (trace elements and rare earths) imply that Cuddapah Basin seawater and dolomitizing fluids were anoxic and ferruginous but not euxinic. Geochemical analyses also indicate that the burial diagenetic fluids evolved from Eu-enriched seawater that probably resulted from continental rifting around 1.9-2.0 Ga. This probable ocean chemistry is in contrast with the anoxic, ferruginous and extremely high Mg/Ca "dolomite oceans" that prevailed during Proterozoic time. The Vempalle dolomite shows more similarities with dolomitised Phanerozoic platform carbonates than typical Precambrian dolomite with its well-preserved textures and burial dolospar cements.

Multi-element crush-leach analysis of H2O-CO2 inclusion fluids from a suite of six vein samples from gold-quartz veins in the Brusson district demonstrates that their solute chemistry (c. 5 wt.% NaCl equivalent) is dominated by sodium chloride with lesser amounts of calcium bicarbonate, potassium chloride and sodium bicarbonate. The samples have been analysed both for gas species (CO2, H2O, N2 and H2S) and for Na, K, Li, Rb, Ca, Mg, Sr, Ba, Fe, Mn, Zn, Pb, Cu, Al, As, B, SO42−, F, Cl, Br and I. The fluids contain appreciable H2S (>10−3 molal), which correlates with the contents of As, CO2 and B. Concentrations of many cations remain similar irrespective of wall rock, but there is evidence of leaching of Li, and possibly I, from some wall rocks. Large variations in the K-content of the fluid may result from precipitation of sericite. The bicarbonate concentrations in the fluids, estimated from charge imbalance, are substantially less than their total CO2 content when trapped as si...

Low-grade metamorphic rocks are known for their low mechanical strength and high weatherability. In the Quadrilátero Ferrífero, an important mineral province located in southeastern Brazil, this set of features results in frequent issues with mining and road slope instability, mainly associated with phyllites. Despite the significant iron ore production that occurs in this province, little is known about the geotechnical properties of the materials constituting the weathering front. Here, we report work aimed at investigating the changes in the basic properties of phyllites at four weathering grades. The methodology used included the field classification and mapping of four weathering grades in order to assess their spatial distribution on a road slope, as well as sampling for geological characterization by petrography and X-ray diffraction (XRD). In addition, the authors performed a physical characterization of all weathering grades, including index properties, mercury porosimetry, and strength data obtained with a Schmidt hammer both in the field and in the laboratory as well as using the point load test (PLT). Results showed the relevance of structural features such as discontinuities and metamorphic foliation observed in the weathering morphology in situ, with different weathering intensities occurring along the slope. Changes in the porosity and pore size distribution in the weathering front were nonlinear, as were resistance variations. The difficulty involved in performing the macroscopic identification of weathering grades due to the very fine texture of the rock as well as microstructural heterogeneities are likely causes of the observed variability in phyllite properties. This fundamental knowledge may aid the prediction of short-term and long-term scenarios for slope stability based on rock weatherability.

A new methodology based on a portable X-ray fluorescence (pXRF) was applied in this work to analyze the geochemical dispersion halo of a sulfide mineralization along the Bule Stream sediments (Ouro Branco, Minas Gerais State, Brazil). The study area, located in the Iron Quadrangle (QF), has an important sulfide occurrence of antimony and zinc, which was explored between 1920s and 1930s. Stream sediment samples were collected along the Bule Stream and from some of its tributaries. Aluminum, Fe, Ca, Mg, Mn and Ti contents were obtained by the pXRF “mining mode” and quantified in percentage (%), while the results for Cu, Zn, Pb, As, Cr, Ag, Sb and Sr were carried out by the pXRF “soil mode”, quantified in parts per million (ppm). The statistical treatment of data by Spearman correlation based on geochemical data and some sediment features were discussed, such as the geochemical affinities between the analyzed elements and supergene processes which control the elemental dispersion. Alum...

The Palaeoproterozoic Vempalle Formation of the Cuddapah Basin, India, significantly adds to our understanding of the evolution of Precambrian marine carbonate systems and the redox state of the Earth's early oceans. A faciesmicrofacies-diagenetic-geochemical examination of samples from a 900-m long exposure in a freshly-cut canal section shows that 10 to 15 % of precursor limestone is still preserved in the Vempalle Formation in the form of remnant patches of calcimicrite and ooids with calcite spar cement. The ooids, preserving primary radial and concentric fabrics and radial fractures, are considered to have been originally precipitated as calcite, which may have been low-Mg. In places the preserved calcite spar, that is partially replaced by fabric-destructive dolomite, shows Type I calcite twin lamellae. Petrographic observations demonstrate that Vempalle Formation dolomite formed through very early precipitation, which in stromatolites preserved microbial filaments, as well as through fabric-destructive dolomitization during shallow to moderate burial. Vempalle Formation dolomite is characterized by micritic dolomite crystals which suggest rapid early dolomitization of lime mud and micritic calcite from a supersaturated Mg-Ca-rich solution, probably near-surface or during shallow burial. Depletion of Na and Sr contents of Vempalle Formation dolomite along with negative 18O values indicate dolomite recrystallisation during burial and further replacement. Dolomite 13C values of-0.5 to 2 ‰ are likely inherited original marine values. Geochemical proxies (trace elements and rare earths) imply that Cuddapah Basin seawater and dolomitizing fluids were anoxic and ferruginous but not euxinic. Geochemical analyses also indicate that the burial diagenetic fluids evolved from Eu-enriched seawater that probably resulted from continental rifting around 1.9-2.0 Ga. This probable ocean chemistry is in contrast with the anoxic, ferruginous and extremely high Mg/Ca "dolomite oceans" that prevailed during Proterozoic time. The Vempalle dolomite shows more similarities with dolomitised Phanerozoic platform carbonates than typical Precambrian dolomite with its well-preserved textures and burial dolospar cements.

The Palaeoproterozoic Vempalle Formation of the Cuddapah Basin, India, significantly adds to our understanding of the evolution of Precambrian marine carbonate systems and the redox state of the Earth's early oceans. A faciesmicrofacies-diagenetic-geochemical examination of samples from a 900-m long exposure in a freshly-cut canal section shows that 10 to 15 % of precursor limestone is still preserved in the Vempalle Formation in the form of remnant patches of calcimicrite and ooids with calcite spar cement. The ooids, preserving primary radial and concentric fabrics and radial fractures, are considered to have been originally precipitated as calcite, which may have been low-Mg. In places the preserved calcite spar, that is partially replaced by fabric-destructive dolomite, shows Type I calcite twin lamellae. Petrographic observations demonstrate that Vempalle Formation dolomite formed through very early precipitation, which in stromatolites preserved microbial filaments, as well as through fabric-destructive dolomitization during shallow to moderate burial. Vempalle Formation dolomite is characterized by micritic dolomite crystals which suggest rapid early dolomitization of lime mud and micritic calcite from a supersaturated Mg-Ca-rich solution, probably near-surface or during shallow burial. Depletion of Na and Sr contents of Vempalle Formation dolomite along with negative 18O values indicate dolomite recrystallisation during burial and further replacement. Dolomite 13C values of-0.5 to 2 ‰ are likely inherited original marine values. Geochemical proxies (trace elements and rare earths) imply that Cuddapah Basin seawater and dolomitizing fluids were anoxic and ferruginous but not euxinic. Geochemical analyses also indicate that the burial diagenetic fluids evolved from Eu-enriched seawater that probably resulted from continental rifting around 1.9-2.0 Ga. This probable ocean chemistry is in contrast with the anoxic, ferruginous and extremely high Mg/Ca "dolomite oceans" that prevailed during Proterozoic time. The Vempalle dolomite shows more similarities with dolomitised Phanerozoic platform carbonates than typical Precambrian dolomite with its well-preserved textures and burial dolospar cements.

The Palaeoproterozoic Vempalle Formation of the Cuddapah Basin, India, significantly adds to our understanding of the evolution of Precambrian marine carbonate systems and the redox state of the Earth's early oceans. A faciesmicrofacies-diagenetic-geochemical examination of samples from a 900-m long exposure in a freshly-cut canal section shows that 10 to 15 % of precursor limestone is still preserved in the Vempalle Formation in the form of remnant patches of calcimicrite and ooids with calcite spar cement. The ooids, preserving primary radial and concentric fabrics and radial fractures, are considered to have been originally precipitated as calcite, which may have been low-Mg. In places the preserved calcite spar, that is partially replaced by fabric-destructive dolomite, shows Type I calcite twin lamellae. Petrographic observations demonstrate that Vempalle Formation dolomite formed through very early precipitation, which in stromatolites preserved microbial filaments, as well as through fabric-destructive dolomitization during shallow to moderate burial. Vempalle Formation dolomite is characterized by micritic dolomite crystals which suggest rapid early dolomitization of lime mud and micritic calcite from a supersaturated Mg-Ca-rich solution, probably near-surface or during shallow burial. Depletion of Na and Sr contents of Vempalle Formation dolomite along with negative 18O values indicate dolomite recrystallisation during burial and further replacement. Dolomite 13C values of-0.5 to 2 ‰ are likely inherited original marine values. Geochemical proxies (trace elements and rare earths) imply that Cuddapah Basin seawater and dolomitizing fluids were anoxic and ferruginous but not euxinic. Geochemical analyses also indicate that the burial diagenetic fluids evolved from Eu-enriched seawater that probably resulted from continental rifting around 1.9-2.0 Ga. This probable ocean chemistry is in contrast with the anoxic, ferruginous and extremely high Mg/Ca "dolomite oceans" that prevailed during Proterozoic time. The Vempalle dolomite shows more similarities with dolomitised Phanerozoic platform carbonates than typical Precambrian dolomite with its well-preserved textures and burial dolospar cements.

The stratiform Cu-Co ore mineralisation in the Katangan Copperbelt consists of dispersed sulphides and sulphides in nodules and lenses, which are often pseudomorphs after evaporites. Two types of pseudomorphs can be distinguished in the nodules and lenses. In type 1 examples, dolomite precipitated first and was subsequently replaced by Cu-Co sulphides and authigenic quartz, whereas in type 2 examples, authigenic quartz and Cu-Co sulphides precipitated prior to dolomite and are coarsegrained. The sulphur isotopic composition of the coppercobalt sulphides in the type 1 pseudomorphs is between −10.3 and 3.1‰ relative to the Vienna Canyon Diablo Troilite, indicating that the sulphide component was derived from bacterial sulphate reduction (BSR). The generation of HCO À 3 during this process caused the precipitation and replacement of anhydrite by dolomite. A second product of BSR is the generation of H 2 S, resulting in the precipitation of Cu-Co sulphides from the mineralising fluids. Initial sulphide precipitation occurred along the rim of the pseudomorphs and continued towards the core. Precipitation of authigenic quartz was most likely induced by a pH decrease during sulphide precipitation. Fluid inclusion data from quartz indicate the presence of a high-salinity (8-18 eq. wt.% NaCl) fluid, possibly derived from evaporated seawater which migrated through the deep subsurface. 87 Sr/ 86 Sr ratios of dolomite in type 1 nodules range between 0.71012 and 0.73576, significantly more radiogenic than the strontium isotopic composition of Neoproterozoic marine carbonates (87 Sr/ 86 Sr=0.7056-0.7087). This suggests intense interaction with siliciclastic sedimentary rocks and/or the granitic basement. The low carbon isotopic composition of the dolomite in the pseudomorphs (−7.02 and −9.93‰ relative to the Vienna Pee Dee Belemnite, V-PDB) compared to the host rock dolomite (−4.90 and +1.31‰ V-PDB) resulted from the oxidation of organic matter during BSR.

The stratiform Cu-Co ore mineralisation in the Katangan Copperbelt consists of dispersed sulphides and sulphides in nodules and lenses, which are often pseudomorphs after evaporites. Two types of pseudomorphs can be distinguished in the nodules and lenses. In type 1 examples, dolomite precipitated first and was subsequently replaced by Cu-Co sulphides and authigenic quartz, whereas in type 2 examples, authigenic quartz and Cu-Co sulphides precipitated prior to dolomite and are coarsegrained. The sulphur isotopic composition of the coppercobalt sulphides in the type 1 pseudomorphs is between −10.3 and 3.1‰ relative to the Vienna Canyon Diablo Troilite, indicating that the sulphide component was derived from bacterial sulphate reduction (BSR). The generation of HCO À 3 during this process caused the precipitation and replacement of anhydrite by dolomite. A second product of BSR is the generation of H 2 S, resulting in the precipitation of Cu-Co sulphides from the mineralising fluids. Initial sulphide precipitation occurred along the rim of the pseudomorphs and continued towards the core. Precipitation of authigenic quartz was most likely induced by a pH decrease during sulphide precipitation. Fluid inclusion data from quartz indicate the presence of a high-salinity (8-18 eq. wt.% NaCl) fluid, possibly derived from evaporated seawater which migrated through the deep subsurface. 87 Sr/ 86 Sr ratios of dolomite in type 1 nodules range between 0.71012 and 0.73576, significantly more radiogenic than the strontium isotopic composition of Neoproterozoic marine carbonates (87 Sr/ 86 Sr=0.7056-0.7087). This suggests intense interaction with siliciclastic sedimentary rocks and/or the granitic basement. The low carbon isotopic composition of the dolomite in the pseudomorphs (−7.02 and −9.93‰ relative to the Vienna Pee Dee Belemnite, V-PDB) compared to the host rock dolomite (−4.90 and +1.31‰ V-PDB) resulted from the oxidation of organic matter during BSR.

The Palaeoproterozoic Vempalle Formation of the Cuddapah Basin, India, significantly adds to our understanding of the evolution of Precambrian marine carbonate systems and the redox state of the Earth's early oceans. A faciesmicrofacies-diagenetic-geochemical examination of samples from a 900-m long exposure in a freshly-cut canal section shows that 10 to 15 % of precursor limestone is still preserved in the Vempalle Formation in the form of remnant patches of calcimicrite and ooids with calcite spar cement. The ooids, preserving primary radial and concentric fabrics and radial fractures, are considered to have been originally precipitated as calcite, which may have been low-Mg. In places the preserved calcite spar, that is partially replaced by fabric-destructive dolomite, shows Type I calcite twin lamellae. Petrographic observations demonstrate that Vempalle Formation dolomite formed through very early precipitation, which in stromatolites preserved microbial filaments, as well as through fabric-destructive dolomitization during shallow to moderate burial. Vempalle Formation dolomite is characterized by micritic dolomite crystals which suggest rapid early dolomitization of lime mud and micritic calcite from a supersaturated Mg-Ca-rich solution, probably near-surface or during shallow burial. Depletion of Na and Sr contents of Vempalle Formation dolomite along with negative 18O values indicate dolomite recrystallisation during burial and further replacement. Dolomite 13C values of-0.5 to 2 ‰ are likely inherited original marine values. Geochemical proxies (trace elements and rare earths) imply that Cuddapah Basin seawater and dolomitizing fluids were anoxic and ferruginous but not euxinic. Geochemical analyses also indicate that the burial diagenetic fluids evolved from Eu-enriched seawater that probably resulted from continental rifting around 1.9-2.0 Ga. This probable ocean chemistry is in contrast with the anoxic, ferruginous and extremely high Mg/Ca "dolomite oceans" that prevailed during Proterozoic time. The Vempalle dolomite shows more similarities with dolomitised Phanerozoic platform carbonates than typical Precambrian dolomite with its well-preserved textures and burial dolospar cements.

The Palaeoproterozoic Vempalle Formation of the Cuddapah Basin, India, significantly adds to our understanding of the evolution of Precambrian marine carbonate systems and the redox state of the Earth's early oceans. A faciesmicrofacies-diagenetic-geochemical examination of samples from a 900-m long exposure in a freshly-cut canal section shows that 10 to 15 % of precursor limestone is still preserved in the Vempalle Formation in the form of remnant patches of calcimicrite and ooids with calcite spar cement. The ooids, preserving primary radial and concentric fabrics and radial fractures, are considered to have been originally precipitated as calcite, which may have been low-Mg. In places the preserved calcite spar, that is partially replaced by fabric-destructive dolomite, shows Type I calcite twin lamellae. Petrographic observations demonstrate that Vempalle Formation dolomite formed through very early precipitation, which in stromatolites preserved microbial filaments, as well as through fabric-destructive dolomitization during shallow to moderate burial. Vempalle Formation dolomite is characterized by micritic dolomite crystals which suggest rapid early dolomitization of lime mud and micritic calcite from a supersaturated Mg-Ca-rich solution, probably near-surface or during shallow burial. Depletion of Na and Sr contents of Vempalle Formation dolomite along with negative 18O values indicate dolomite recrystallisation during burial and further replacement. Dolomite 13C values of-0.5 to 2 ‰ are likely inherited original marine values. Geochemical proxies (trace elements and rare earths) imply that Cuddapah Basin seawater and dolomitizing fluids were anoxic and ferruginous but not euxinic. Geochemical analyses also indicate that the burial diagenetic fluids evolved from Eu-enriched seawater that probably resulted from continental rifting around 1.9-2.0 Ga. This probable ocean chemistry is in contrast with the anoxic, ferruginous and extremely high Mg/Ca "dolomite oceans" that prevailed during Proterozoic time. The Vempalle dolomite shows more similarities with dolomitised Phanerozoic platform carbonates than typical Precambrian dolomite with its well-preserved textures and burial dolospar cements.

Multi-element crush-leach analysis of H2O-CO2 inclusion fluids from a suite of six vein samples from gold-quartz veins in the Brusson district demonstrates that their solute chemistry (c. 5 wt.% NaCl equivalent) is dominated by sodium chloride with lesser amounts of calcium bicarbonate, potassium chloride and sodium bicarbonate. The samples have been analysed both for gas species (CO2, H2O, N2 and H2S) and for Na, K, Li, Rb, Ca, Mg, Sr, Ba, Fe, Mn, Zn, Pb, Cu, Al, As, B, SO4 2−, F, Cl, Br and I. The fluids contain appreciable H2S (>10−3 molal), which correlates with the contents of As, CO2 and B. Concentrations of many cations remain similar irrespective of wall rock, but there is evidence of leaching of Li, and possibly I, from some wall rocks. Large variations in the K-content of the fluid may result from precipitation of sericite. The bicarbonate concentrations in the fluids, estimated from charge imbalance, are substantially less than their total CO2 content when trapped as s...

The Lamego orogenic gold deposit (440,742oz gold measured reserves and 2.4milliont measured resources, with an average grade of 5.71g/t Au and a cut-off grade of 2.15g/t Au; AngloGold Ashanti Córrego do Sítio Mineração S/A (AGA) personal communication, 2014) is located in the 5km-long trend that includes the world-class Cuiabá deposit. It is hosted in the Neoarchean metavolcano–sedimentary rocks of the Rio das Velhas greenstone belt, Quadrilátero Ferrífero, Brazil. Mineralization is associated mainly with metachert–banded iron formation (BIF) and carbonaceous phyllites in the reclined Lamego fold, in which the Cabeça de Pedra orebody represents the hinge zone. Mineralization is concentrated in silicification zones and their quartz veins, as well as in sulfide minerals, product of BIF sulfidation. Hydrothermal alteration varies according to host rock, with abundant sulfide–carbonate in BIF, and sericite–chlorite in carbonaceous phyllite. Quartz vein classification according to structural relationships and host rocks identified three vein systems. The V1 system, mainly composed of smoky quartz (Qtz I) and pyrite, is extensional, crosscuts the bedding plane S0 of BIF, and is parallel to the fold axis. The V2 system, of the same composition, is represented by veins that are parallel to the S1–2 foliation and S0. This system is also characterized by silicification zones in the BIF–carbonaceous phyllite contact that has its maximum expression in the hinge zone of folds. The V3 system has milky quartz (Qtz II) veins, which result from the recrystallization of smoky quartz, located mainly in shear zones and faults; these veins form structures en echelon and vein arrays. The most common ore minerals are pyrite, As-pyrite and arsenopyrite. Fluid inclusion-FI trapped in all quartz veins present composition in the H2O–CO2 ±CH4–NaCl system. Fluid evolution can be interpreted in two stages: i) aqueous–carbonic fluid trapped in Qtz I, of low salinity (~2% equiv. wt.% NaCl), and ii) carbonic–aqueous fluid, of moderate salinity (average 9eq.wt.% NaCl) hosted in Qtz II. Both stages are characterized by decrepitation temperatures in the range of 200 to >300°C, and suggest a fluid of metamorphic origin. Applying an arsenopyrite geothermometer, the calculated formation temperature for the Cabeça de Pedra orebody is 300 to 375°C. The vertical intersection of the isochors allows a minimum pressure calculation of 2.6kbar. The composition of individual FIs of this orebody, obtained by LA-ICP-MS analyses, compared with results of FIs for the Carvoaria Velha deposit, Córrego do Sítio lineament, highlights a standard composition typical of metamorphic fluids with Na>K>Ca>Mg, which increase or decrease in concentration as a function of salinity in both deposits. Trace elements vary according to fluid–rock reactions, and are directly related to the host rock composition. The comparison of data sets of the two deposits shows that the Cabeça de Pedra FIs have a higher enrichment in Zn, while Cu, As and Sb are richer in Carvoaria Velha, suggesting influence of the host rock geochemistry. The suggested mechanisms for gold precipitation at the Cabeça de Pedra orebody, Lamego gold deposit are: i) hydrolysis of the carbonaceous matter of phyllite and BIF, affecting fO2, destabilizing sulfur complexes and enhancing gold precipitation; ii) replacement of BIF iron carbonates by sulfides; and iii) continuous pressure changes that lead to silica precipitation and free gold. Other than playing the long-recognized role of the carbonaceous phyllites as a fluid barrier, the data highlight their importance as a source of metals.