Potential environmental impact at São Domingos mining district (Iberian Pyrite Belt,SW Iberian Peninsula): evidence from a chemical and mineralogical characterization

São Domingos like other long-term activity mines of the Iberian Pyrite Belt (IPB) dating back to pre-Roman times, is supposed to produce considerable amounts of mining wastes which cause significant downstream negative environment impact related to the acid mine drainage (AMD) production and high content of potentially toxic metals and metalloids in Chanza and Guadiana Rivers. The AMD production of a given mining waste depends on the ratio of its acid production to neutralizing phases. In this work, a chemical and mineralogical characterization of the sulphide-rich wastes from São Domingos has been developed to discriminate which residues are the main sources of AMD generation. A total of 47 representative samples of the different residue types were collected to estimate their possible contamination hazards through detailed studies of (1) for a mineralogical characterization: reflected-light optical microscope, scanning electron microscope (SEM) and XRD analysis; and (2) for a chemical characterization: bulk-rock analysis. AMD prediction by the standard acid-base accounting method (ABA) was used in order to determine the acidification potential of each residue type. This study also offers an estimation of the contribution of toxic elements to the environment, being thus, a base for future remediation actions at São Domingos and other abandoned massive sulphide mines within the IPB.     

U–Pb geochronology and Hf isotope ratios of magmatic zircons from the Iberian Pyrite Belt

A geochronology and Hf isotope study, using laser ablation-ICP-MS analysis of zircon grains, has been conducted to date felsic volcanic rocks from the Portuguese sector of the Iberian Pyrite Belt and to establish possible sources for these rocks. The ages obtained range from the Famennian to the Tournaisian, with the oldest ages reported in the Belt so far being identified in its southwestern part (Cercal area). Results also indicate that within each area, volcanism may have extended for significant periods of time. This suggests that caution is needed in interpreting possible migration trends for the volcanism, as the exact stratigraphic position of the sampled rocks is not always clear. Despite of this, the new data, coupled with previously reported information, suggests that volcanism migrated within the basin from the southwest to the northeast (present day coordinates). Projection from initial zircon ?Hf values towards the depleted mantle evolution curve, via an intermediate reservoir, allows the calculation of Hf protolith model ages that are predominantly Meso-Proterozoic. This is compatible with acid magmas resulting from the fusion of Phyllite–Quartzite (PQ) Formation metasedimentary rocks, which are beneath the volcanic rocks. This is because zircon grains from one PQ Formation sample provided Late Neo-Proterozoic ages and Paleo-Proterozoic to Late Archean U–Pb ages, and the Hf isotope signatures of these zircons can be expected to mix during fusion and result in protolith model ages that would be intermediate between the two U–Pb age populations, as recorded. Further supporting this source for the magmas, the distribution of U–Pb ages of (pre-Variscan) inherited zircon grains in the volcanic rocks is very similar to that shown by the detrital zircon grains from a PQ sample.     

Helium, lead and sulfur isotope geochemistry of the Gejiu Sn-polymetallic ore deposit and the sources of ore-forming materials

Studies on the helium, lead and sulfur isotopic composition were performed of the Gejiu super-large Sn-polymetallic ore deposit. The results indicated that the ore-forming materials came from different sources and the deposit is a product of superimposed mineralization. The deposit is characterized by multi-source and multi-period mineralization, which experienced submarine hydrothermal deposition and Late Yanshanian magmatic hydrothermal mineralization. It is held that the Gejiu super-large Sn-polymetallic ore deposit is a multi-genesis deposit.     

Geology of the Rosário–Neves Corvo antiform, Iberian Pyrite Belt, Portugal: new insights from physical volcanology, palynostratigraphy and isotope geochronology studies

The lithostratigraphic sequence in the Rosário–Neves Corvo antiform comprises the Phyllite–Quartzite Group, whose top is of Famennian age, the Volcanic Sedimentary Complex, of Strunian to upper Visean age, and the Mértola Formation (the lower unit of the Baixo Alentejo Flysch Group) of upper Visean age. The volcanic sedimentary complex comprises a lower sequence of Strunian (Late Famennian) age and an upper sequence of lower to upper Visean age. Detailed mapping of the antiform towards NW of the Neves Corvo mine, supported by palynological dating, identified two new lithostratigraphic units: the Barrancão member (upper Famennian) ascribed to the Phyllite–Quartzite Group and made up of laminated dark shales with siliceous lenses and nodules, and the Ribeira de Cobres Formation of the Volcanic Sedimentary Complex, containing shales, siltstones and fine volcaniclastic rocks. Based on zircon U–Pb isotope dating, five discrete felsic magmatic events were identified at approximately 354, 359, 365, 373 and 384 Ma. This suggests that the volcanic activity in the area has extended for about 30 Ma, in a context of high regional heat flow as indicated by the geochemical signatures of the felsic volcanic rocks. The characteristics of magmatism and the depositional environment indicated by the sedimentary record should therefore have been highly favourable for massive sulphide formation. However, evidence of massive sulphide mineralization in the study area is still to be found. Moreover, reconstruction of the volcanic facies architecture demonstrated that the volcanic units in the Rosário area are strongly dominated by coherent facies typical of the inner part of thick lavas/domes. In fact, most of their external part, the more favourable location for possible massive sulphide mineralization, is missing. Palynological dating indicates a significant hiatus, recognised between the lower and upper sequences of the volcanic sedimentary complex, which implies erosion of the top of the volcanic centre, where VHMS deposits could possibly have formed. However, lateral areas of this volcanic centre, eventually preserved at depth, have good potential to host massive sulphide mineralization.     

Isotope geochemistry of ore fluids for the Dongsheng sandstone-type uranium deposit, China

The Dongsheng sandstone-type uranium deposit is one of the large-sized sandstone-type uranium deposits discovered in the northern part of the Ordos Basin of China in recent years. Geochemical characteristics of the Dongsheng uranium deposit are significantly different from those of the typical interlayered oxidized sandstone-type uranium ore deposits in the region of Middle Asia. Fluid inclusion studies of the uranium deposit showed that the uranium ore-forming temperatures are within the range of 150–160℃. Their 3He/4He ratios are within the range of 0.02–1.00 R/Ra, about 5–40 times those of the crust. Their 40Ar/36Ar ratios vary from 584 to 1243, much higher than the values of atmospheric argon. The δ18OH2O and δD values of fluid inclusions from the uranium deposit are -3.0‰– -8.75‰ and -55.8‰– -71.3‰, respectively, reflecting the characteristics of mixed fluid of meteoric water and magmatic water. The δ18OH2O and δD values of kaolinite layer at the bottom of the uranium ore deposit are 6.1‰ and -77‰, respectively, showing the characteristics of magmatic water. The δ13CV-PDB and δ18OH2O values of calcite veins in uranium ores are -8.0‰ and 5.76‰, respectively, showing the characteristics of mantle source. Geochemical characteristics of fluid inclusions indicated that the ore-formation fluid for the Dongsheng uranium deposit was a mixed fluid of meteoric water and deep-source fluid from the crust. It was proposed that the Jurassic-Cretaceous U-rich metamorphic rocks and granites widespread in the northern uplift area of the Ordos Basin had been weathered and denudated and the ore-forming elements, mainly uranium, were transported by meteoric waters to the Dongsheng region, where uranium ores were formed. Tectonothermal events and magmatic activities in the Ordos Basin during the Mesozoic made fluids in the deep interior and oil/gas at shallow levels upwarp along the fault zone and activated fractures, filling into U-bearing clastic sandstones, thus providing necessary energy for the formation of uranium ores.     

Geology,isotope geochemistry and ore genesis of the Shanshulin carbonate-hosted Pb–Zn deposit,southwest China

The Shanshulin Pb–Zn deposit occurs in Upper Carboniferous Huanglong Formation dolomitic limestone and dolostone, and is located in the western Yangtze Block, about 270 km west of Guiyang city in southwest China. Ore bodies occur along high angle thrust faults affiliated to the Weishui regional fault zone and within the northwestern part of the Guanyinshan anticline. Sulfide ores are composed of sphalerite, pyrite, and galena that are accompanied by calcite and subordinate dolomite. Twenty-two ore bodies have been found in the Shanshulin deposit area, with a combined 2.7 million tonnes of sulfide ores grading 0.54 to 8.94 wt.% Pb and 1.09 to 26.64 wt.% Zn. Calcite samples have δ¹³C_PDB and δ¹⁸O_SMOW values ranging from − 3.1 to + 2.5‰ and + 18.8 to + 26.5‰, respectively. These values are higher than mantle and sedimentary organic matter, but are similar to marine carbonate rocks in a δ¹³C_PDB vs. δ¹⁸O_SMOW diagram, suggesting that carbon in the hydrothermal fluid was most likely derived from the carbonate country rocks. The δ³⁴S_CDT values of sphalerite and galena samples range from + 18.9 to + 20.3‰ and + 15.6 to + 17.1‰, respectively. These values suggest that evaporites are the most probable source of sulfur. The δ³⁴S_CDT values of symbiotic sphalerite–galena mineral pairs indicate that deposition of sulfides took place under chemical equilibrium conditions. Calculated temperatures of S isotope thermodynamic equilibrium fractionation based on sphalerite–galena mineral pairs range from 135 to 292 °C, consistent with previous fluid inclusion studies. Temperatures above 100 °C preclude derivation of sulfur through bacterial sulfate reduction (BSR) and suggest that reduced sulfur in the hydrothermal fluid was most likely supplied through thermo-chemical sulfate reduction (TSR). Twelve sphalerite samples have δ⁶⁶Zn values ranging from 0.00 to + 0.55‰ (mean + 0.25‰) relative to the JMC 3-0749L zinc isotope standard. Stages I to III sphalerite samples have δ⁶⁶Zn values ranging from 0.00 to + 0.07‰, + 0.12 to + 0.23‰, and + 0.29 to + 0.55‰, respectively, showing the relatively heavier Zn isotopic compositions in later versus earlier sphalerite. The variations of Zn isotope values are likely due to kinetic Raleigh fractional crystallization. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios of the sulfide samples fall in the range of 18.362 to 18.573, 15.505 to 15.769 and 38.302 to 39.223, respectively. The Pb isotopic ratios of the studied deposit plot in the field that covers the upper crust, orogenic belt and mantle Pb evolution curves and overlaps with the age-corrected Proterozoic folded basement rocks, Devonian to Lower Permian sedimentary rocks and Middle Permian Emeishan flood basalts in a ²⁰⁷Pb/²⁰⁴Pb vs. ²⁰⁶Pb/²⁰⁴Pb diagram. This observation points to the derivation of Pb metal from mixed sources. Sphalerite samples have ⁸⁷Sr/⁸⁶Sr_200 Ma ratios ranging from 0.7107 to 0.7115 similar to the age-corrected Devonian to Lower Permian sedimentary rocks (0.7073 to 0.7111), higher than the age-corrected Middle Permian basalts (0.7039 to 0.7078), and lower than the age-corrected Proterozoic folded basement (0.7243 to 0.7288). Therefore, the Sr isotope data support a mixed source. Studies on the geology and isotope geochemistry suggest that the Shanshulin deposit is a carbonate-hosted, thrust fault-controlled, strata-bound, epigenetic, high grade deposit formed by fluids and metals of mixed origin.     

Mineralogy and trace-element geochemistry of the high-grade iron ores of the Águas Claras Mine and comparison with the Capão Xavier and Tamanduá iron ore deposits, Quadrilátero Ferrífero, Brazil

Several major iron deposits occur in the Quadrilátero Ferrífero (QF), southeastern region of Brazil, where metamorphosed and heterogeneously deformed banded iron formation (BIF) of the Cauê Formation, regionally called itabirite, was transformed into high- (Fe >64%) and low-grade (30%?2O₃, with a higher amount of detrimental impurities, especially MnO, in the soft ore. Both hard and soft ores are depleted in trace elements. The high-grade ores at the Águas Claras Mine have at least a dual origin, involving hypogene and supergene processes. The occurrence of the hard, massive high-grade ore within “fresh” dolomitic itabirite is evidence of its hypogene origin. Despite the contention about the origin of the dolomitic itabirite (if this rock is a carbonate-rich facies of the Cauê Formation or a hematite–carbonate precursor of the soft high-grade ore), mineralogical and geochemical features of the soft high-grade ore indicate that it was formed by leaching of dolomite from the dolomitic itabirite by meteoric water. The comparison of the Águas Claras, Capão Xavier and Tamanduá orebodies shows that the original composition of the itabiritic protore plays a major role in the genesis of high- and low-grade soft ores in the QF. Under the same weathering and structural conditions, the dolomitic itabirite is the more favorable to form high-grade deposits than siliceous itabirite. Field relations at the Águas Claras and Capão Xavier deposits suggest that it is not possible to form huge soft high-grade supergene deposits from siliceous itabirite, unless another control, such as impermeable barriers, had played an important role. The occurrence in the Tamanduá Mine of a large, soft, high-grade orebody formed from siliceous itabirite and closely associated with hypogene hard ore suggests that large, soft, high-grade orebodies of the Quadrilátero Ferrífero, which occur within siliceous itabirite, have a hypogene contribution in their formation.     

Petrology and geochemistry of calc-alkaline volcanic and subvolcanic rocks,Dalli porphyry copper–gold deposit,Markazi Province,Iran

Early Miocene igneous rocks associated with the Dalli porphyry ore body are exposed within the Urumieh-Dokhtar Magmatic Arc (UDMA). The Dalli porphyry Cu–Au deposit is hosted by subduction-related subvolcanic plutons with chemical composition from diorite to granodiorite, which intruded andesitic and dacitic volcanic rocks and a variety of sedimentary sequences. ⁴⁰Ar/³⁹Ar age data indicate a minimum emplacement age of ～21 million years for a potasically altered porphyritic diorite that hosts the porphyry system. The deposit has a proven reserve of 8 million tonnes of rock containing 0.75 g/t Au and 0.5% Cu. Chondrite-normalized rare earth element (REE) patterns for the subvolcanic rocks are characterized by light REE enrichments [(La/Sm) _n ?=?2.57–6.40] and flat to gently upward-sloping profiles from middle to heavy REEs [(Dy/Yb) _n ?=?0.99–2.78; (Gd/Yb) _n ?=?1.37–3.54], with no significant Eu anomalies. These characteristics are generated by the fractionation of amphibole and the suppression of plagioclase crystallization from hydrous calc-alkaline magmas. In normalized multi-element diagrams, all analysed rocks are characterized by enrichments in large ion lithophile elements and depletions in high field strength elements, and display typical features of subduction-related calc-alkaline magmas. We used igneous mineral compositions to constrain the conditions of crystallization and emplacement. Biotite compositions plot above the nickel–nickel oxide (NNO) buffer and close to oxygen fugacity values defined by the hematite–magnetite (HM) buffer, indicating oxidizing conditions during crystallization. Assuming a minimum crystallization temperature of 775°C, the oxygen (fO₂) and water (fH₂O) fugacities are estimated to be 10^?10.3 bars (～ΔNNO+4) and ≤748 bars, respectively, during the crystallization of biotite phenocrysts. The temperature and pressure conditions, estimated from temperature–corrected Al-in-hornblende barometry and amphibole-plagioclase thermometry, suggest that the hornblende phenocrysts in Dalli rocks crystallized at around 780 ± 20°C and 3.8 ± 0.4 kbar. An alternative method using the calcic amphibole thermobarometer indicates that the Dalli magmas were, on average, characterized by an H₂O content of 4.3 wt.%, a relatively high oxygen fugacity of 10^?11.0 bars (ΔNNO+1.3), and a hornblende phenocryst crystallization temperature of 880 ± 68°C and pressure of 2.6 ± 1.7 kbar.     

Mineralogy,alteration patterns,geochemistry, and fluid properties of the Ag-Au epithermal deposit Nová Baňa,Slovakia

Mineralogy and Petrology - In this contribution, we report new data on mineralogy, alteration patterns, geochemistry, fluid properties and source of fluids for the deposit Nová Baňa, one...     

Monitoring study of the mine pond reclamation of Mina Concepción, Iberian Pyrite Belt (Spain)

Mining of massive (Cu, Pb and Zn) sulphide bodies in the Iberian Pyrite Belt (SW Spain) has generated a great number of abandoned waste deposits such as mine ponds. These represent large accumulations of reactive minerals and subsequently, emission sources of trace elements and formation of acid drainage. Even if they have been restored, monitoring studies are required to evaluate the corrective effects and how they may change over time. This work presents the results of a monitoring study carried out at Mine Concepción mine pond, based on mineralogical (XRD), geochemical (INAA, X-ray fluorescence, ICP-MS) and geophysical (electrical resistivity tomography) techniques. In it, a series of relevant parameters have been well delimited, such as the infilling thickness and its variation and, the position, geometry and absence of water leakages through the base of the mine pond. Additionally, the existence of an internal, remnant flow of acid waters that tends to come out through the pond dyke has been identified. Chemistry of these waters indicates that oxidation processes affecting the Mina Concepción mine tailings are generating acid drainage waters which could potentially release substantial amounts of trace elements to the river Odiel. Thus, giving that not complete sealing is accomplished by the restoration capping and rainfall water infiltrates into the pond materials, at least the sealing of the dyke through which leakages occur should be revised.     

New data on ore geochemistry of the Rodionovskoe gold–quartz deposit,Northeast Russia

The enrichment of gold–quartz ores from the Rodionovskoe deposit in chalcophile elements (Au, Ag, As, Sb) is established. The ores are characterized by small negative Eu anomalies and low REE contents, which are typical of magmatic fluids. Slight enrichment of ores in Bi is evidence of the possible involvement of magmatic fluid in ore formation, which may have been superimposed on early metamorphic quartz veins and veinlets. The variously oriented REE patterns also indicate the presence of another magmatic fluid source, which could be related to the post-ore granitic intrusion. These results generally confirm the metamorphic–magmatic model of the formation of the gold–quartz deposits of the Yana–Kolyma belt. Our data are of practical interest for regional metallogenic forecasts, search, and evaluation of gold deposits.     

Mineralogy, geochemistry and stratigraphy of the Maslovsky Pt–Cu–Ni sulfide deposit, Noril’sk Region, Russia

We report new data on the stratigraphy, mineralogy and geochemistry of the rocks and ores of the Maslovsky Pt–Cu–Ni sulfide deposit which is thought to be the southwestern extension of the Noril’sk 1 intrusion. Variations in the Ta/Nb ratio of the gabbro-dolerites hosting the sulfide mineralization and the compositions of their pyroxene and olivine indicate that these rocks were produced by two discrete magmatic pulses, which gave rise to the Northern and Southern Maslovsky intrusions that together host the Maslovsky deposit. The Northern intrusion is located inside the Tungusska sandstones and basalt of the Ivakinsky Formation. The Southern intrusion cuts through all of the lower units of the Siberian Trap tuff-lavas, including the Lower Nadezhdinsky Formation; demonstrating that the ore-bearing intrusions of the Noril’sk Complex post-date that unit. Rocks in both intrusions have low TiO₂ and elevated MgO contents (average mean TiO₂ <1 and MgO?=?12?wt.%) that are more primitive than the lavas of the Upper Formations of the Siberian Traps which suggests that the ore-bearing intrusions result from a separate magmatic event. Unusually high concentrations of both HREE (Dy+Yb+Er+Lu) and Y (up to 1.2 and 2.1?ppm, respectively) occur in olivines (Fo_79.5 and 0.25% NiO) from picritic and taxitic gabbro-dolerites with disseminated sulfide mineralization. Thus accumulation of HREE, Y and Ni in the melts is correlated with the mineral potential of the intrusions. The TiO₂ concentration in pyroxene has a strong negative correlation with the Mg# of both host mineral and Mg# of host rock. Sulfides from the Northern Maslovsky intrusion are predominantly chalcopyrite–pyrrhotite–pentlandite with subordinate and minor amounts of cubanite, bornite and millerite and a diverse assemblage of rare precious metal minerals including native metals (Au, Ag and Pd), Sn–Pd–Pt–Bi–Pb compounds and Fe–Pt alloys. Sulfides from the Southern Maslovsky intrusion have δ ³⁴S?=?5–6‰ up to 10.8‰ in two samples whereas the country rock basalt have δ ³⁴S?=?3–4‰, implying there was no in situ assimilation of surrounding rocks by magmas.     

Mineralogy and geochemistry of Al-phosphate and Al-borosilicate-bearing metaquartzites of the northern Serra do Espinhaço (State of Bahia, Brazil)

Summary The investigated Al-phosphate- and Al-borosilicate-bearing metaquartzite horizon belongs to the Middle Proterozoic Serra de Vereda member of the São Marcos Formation of the northern Espinhaço fold belt. Outcrops are located in the NNW–SSE trending hills of the Serra de Canas/Cana Brava (Northern Serra do Espinhaço, State of Bahia, NE Brazil) about 10km west of the town of Boquira. Sky blue lazulite and deep blue to lilac dumortierite are enriched in layers which sometimes show relic cross bedding. The occurrence of hematite patches and layers is typical. In rocks of type A, phosphorus contents range from 1.89wt.% to 10.73wt.% P₂O₅ and boron contents are mostly below 10ppm whereas in the rocks of type B phosphorus contents are below 1% and boron contents reach 2600ppm with a mean value of 1139ppm. REE distribution patterns of rocks are predominantly controlled by the amount of xenotime, monazite and zircon. Oxygen thermometry on quartz and hematite and the stability of kyanite, augelite, trolleite and berlinite allow to estimate the minimum metamorphic peak P-T conditions at 475°C and 3.8kbar i.e. within the stability field of scorzalite–lazulite and dumortierite. The association of Al-phosphates with hematite layers provides evidence for the deposition of the metaquartzite protolith in a seawater-fed sabkha-like sand flat fringing the Espinhaço rift. It is proposed that apatite, Al-phosphates and Al-borosilicates were chemically precipitated together with iron hydroxides from pore fluids. The antithetic behaviour of phosphorus and boron contents in the metaquartzites is the consequence of an influx of toxic boron-rich water that drastically affected algae populations and consequently reduced phosphorus precipitation.     

Electron microprobe analyses of ore minerals and H–O,S isotope geochemistry of the Yuerya gold deposit,eastern Hebei,China: Implications for ore genesis and mineralization

The Yuerya gold deposit in eastern Hebei Province, China, is located on the eastern margin of the North China Craton and is hosted by Mesozoic Yanshanian granitoid rocks and adjacent Mesoproterozoic Gaoyuzhuang Formation carbonates. The auriferous quartz veins in this deposit are dominated by pyrite, with subordinate sphalerite, chalcopyrite, and galena in a quartz-dominated gangue that also contains calcite, dolomite, barite, apatite, and fluorite. Gold is present as native gold and electrum, which are generally present as micron-size infillings in microfissures within pyrite and less commonly as tiny inclusions within pyrite, quartz, and tellurobismuthite. The pyrite in this deposit has high Co/Ni ratios and contains elevated concentrations of both of these elements, suggesting that the Yuerya gold deposit has a magmato-hydrothermal origin and that the ore-forming fluids that formed the deposit leached trace elements such as Co, Ni, As, and Au during passage through Archean metamorphic rocks, Mesoproterozoic carbonates, and the Yanshanian Yuerya granitoid. Pyrite in the study area has S/Se ratios and S isotopic compositions that suggest that the sulfur (and by inference the gold) within the deposit was sourced from magmato-hydrothermal fluids that were probably originally derived from Archean metamorphic rocks and Yanshanian granitoids. Tellurobismuthite in the study area is closely intergrown with gold and was the single telluride phase identified during this study. The fineness of gold associated with tellurobismuthite is greater than the fineness of gold associated with pyrite, although the fine particle size of the gold surrounded by tellurobismuthite means that the recovery of this gold is difficult, in turn meaning that the tellurobismuthite has little significance to the economics of the Yuerya gold deposit. Only trace amounts of sulfides are associated with the tellurobismuthite within the Yuerya gold deposit, suggesting that this mineral was deposited under conditions of low fS₂ and/or high fTe₂. In addition, the presence of tellurides within the Yuerya gold deposit reflects a genetic relationship between the deposit and magmatism. Quartz from mineralized veins in the study area has δ¹⁸O values of 11.2‰–12.9‰ and the fluids that formed these veins have δD values of − 78.3‰ to − 72.1‰. The δ³⁴S values of pyrite within the deposit are rather restricted (2.3‰–3.5‰). These data, combined with the trace element geochemistry of sulfides within the deposit, suggest that the formation of the Yuerya gold deposit was closely related to both Archean metamorphic rocks and the Yanshanian Yuerya granitoid.     

Genetic Mineralogy of Pyrite from Jindoushan Gold Deposit,Yantai,Shandong Province

This paper deals with the genetic mineralogy of pyrite from the Jindoushan gold deposi.As a predominant gold-bearing mineral,pyrite bears lots of information about mineralization,which can be elucidated throug the study of mineralogical characters such as crystal form,chemical composiion,thermo-electrical coefficient,etc.In addition,the detailed genetic mineralogy data of pyrite can also help evaluate the prospects of gold deposits.     

Magnetite geochemistry of the Longqiao and Tieshan Fe–(Cu) deposits in the Middle-Lower Yangtze River Belt: Implications for deposit type and ore genesis

Magnetite is a common mineral in many ore deposits and their host rocks, and contains a wide range of trace elements (e.g., Ti, V, Mg, Cr, Mn, Ca, Al, Ni, Ga, Sn) that can be used for deposit type fingerprinting. In this study, we present new magnetite geochemical data for the Longqiao Fe deposit (Luzong ore district) and Tieshan Fe–(Cu) deposit (Edong ore district), which are important magmatic-hydrothermal deposits in eastern China.Textural features, mineral assemblages and paragenesis of the Longqiao and Tieshan ore samples have suggested the presence of two main mineralization periods (sedimentary and hydrothermal) at Longqiao, among which the hydrothermal period comprises four stages (skarn, magnetite, sulfide and carbonate); whilst the Tieshan Fe–(Cu) deposit comprises four mineralization stages (skarn, magnetite, quartz-sulfide and carbonate).Magnetite from the Longqiao and Tieshan deposits has different geochemistry, and can be clearly discriminated by the Sn vs. Ga, Ni vs. Cr, Ga vs. Al, Ni vs. Al, V vs. Ti, and Al vs. Mg diagrams. Such difference may be applied to distinguish other typical skarn (Tieshan) and multi-origin hydrothermal (Longqiao) deposits in the MLYRB. The fluid–rock interactions, influence of the co-crystallizing minerals and other physicochemical parameters, such as temperature and fO₂, may have altogether controlled the magnetite trace element contents of both deposits. The Tieshan deposit may have had higher degree of fO₂, but lower fluid–rock interactions and ore-forming temperature than the Longqiao deposit. The TiO₂–Al₂O₃–(MgO + MnO) and (Ca + Al + Mn) vs. (Ti + V) magnetite discrimination diagrams show that the Longqiao Fe deposit has both sedimentary and hydrothermal features, whereas the Tieshan Fe–(Cu) deposit is skarn-type and was likely formed via hydrothermal metasomatism, consistent with the ore characteristics observed.     

S,Pb, and Sr isotope geochemistry and genesis of Pb–Zn mineralization in the Huangshaping polymetallic ore deposit of southern Hunan Province,China

The Huangshaping Pb–Zn–W–Mo polymetallic deposit, located in southern Hunan Province, China, is one of the largest deposits in the region and is unique for its metals combination of Pb–Zn–W–Mo and the occurrence of significant reserves of all these metals. The deposit contains disseminated scheelite and molybdenite within a skarn zone located between Jurassic granitoids and Carboniferous sedimentary carbonate, and sulfide ores located within distal carbonate-hosted stratiform orebodies. The metals and fluids that formed the W–Mo mineralization were derived from granitoids, as indicated by their close spatial and temporal relationships. However, the source of the Pb–Zn mineralization in this deposit remains controversial.Here, we present new sulfur, lead, and strontium isotope data of sulfide minerals (pyrrhotite, sphalerite, galena, and pyrite) from the Pb–Zn mineralization within the deposit, and these data are compared with those of granitoids and sedimentary carbonate in the Huangshaping deposit, thereby providing insights into the genesis of the Pb–Zn mineralization. These data indicate that the sulfide ores from deep levels in the Huangshaping deposit have lower and more consistent δ³⁴S values (− 96 m level: + 4.4‰ to + 6.6‰, n = 13) than sulfides within the shallow part of the deposit (20 m level: + 8.3‰ to + 16.3‰, n = 19). The δ³⁴S values of deep sulfides are compositionally similar to those of magmatic sulfur within southern Hunan Province, whereas the shallower sulfides most likely contain reduced sulfur derived from evaporite sediments. The sulfide ores in the Huangshaping deposit have initial ⁸⁷Sr/⁸⁶Sr ratios (0.707662–0.709846) that lie between the values of granitoids (0.709654–0.718271) and sedimentary carbonate (0.707484–0.708034) in the Huangshaping deposit, but the ratios decreased with time, indicating that the ore-forming fluids were a combination of magmatic and formation-derived fluids, with the influence of the latter increasing over time. The lead isotopic compositions of sulfide ores do not correlate with sulfide type and define a linear trend in a ²⁰⁷Pb/²⁰⁴Pb vs. ²⁰⁶Pb/²⁰⁴Pb diagram that is distinct from the composition of the disseminated pyrite within sedimentary carbonates and granitoids in the Huangshaping deposit, but is similar to the lead isotopic composition of sulfides within coeval skarn Pb–Zn deposits in southern Hunan Province. In addition, the sulfide ores have old signatures with relative high ²⁰⁷Pb/²⁰⁶Pb ratios, suggesting that the underlying Paleoproterozoic basement within southern Hunan Province may be the source of metals within the Huangshaping deposit.The isotope geochemistry of sulfide ores in the Huangshaping deposit shows a remarkable mixed source of sulfur and ore-forming fluids, and the metals were derived from the basement. These features are not found in representative skarn-type Pb–Zn mineralization located elsewhere. The ore-forming elements (S, Pb, and Zn) from the granitoids made an insignificant contribution to sulfide precipitation in this deposit. However, the emplacement of granitoids did provide large amounts of heat and fluids to the hydrothermal system in this area and extracted metals from the basement rocks, indicating that the Jurassic magmatism associated with the Huangshaping deposit was crucial to the Pb–Zn mineralization.     

Sulphur- and lead-isotope geochemistry of the Arapuçandere lead–zinc–copper deposit,Biga Peninsula,northwest Turkey

The Arapuçandere Pb–Zn–Cu ore body is a typical vein-type lead–zinc deposit of the Biga Peninsula, and is currently being mined for lead and zinc. In the study area, Permian–Triassic metamorphic rocks, Triassic metaclastic and metabasic rocks, Oligocene–Miocene granitoids, Miocene volcanic rocks, and Quaternary terrigenous sediments crop out. The ore deposits developed as Pb–Zn–Cu-bearing veins along faults in Triassic metasandstone and metadiabase. Microscopic studies reveal that the veins contain galena, sphalerite, chalcopyrite, pyrite, marcasite, covellite, and specular hematite as ore minerals, and quartz, calcite, and barite as gangue minerals. Analysed sulphur-isotope compositions (δ³⁴S_VCDT) of galena, sphalerite, and chalcopyrite range from ? 5.9 to ? 1.9‰ (average ? 3.4‰), from ? 5.5 to ? 1.7‰ (average ? 4.2 ‰), and from ? 3.5 to ? 0.9‰ (average ? 2.6‰), respectively; that of H₂S in the hydrothermal fluid was in the calculated range of ? 5.8 to +0.1‰ (average ? 2.5‰). These isotopic values suggest that magmatic sulphur dominates in sulphides, mixed with minor, isotopically light sulphur. Because no contemporaneous magmatic activity is associated with mineralization, it may be assumed that sulphur was leached from the surrounding Triassic units, mainly from metabasic, partly from metaclastic rocks. Lead-isotope studies indicate a model age of 114–63 Ma for the lead reservoir, in accord with possible sulphur-bearing local source rocks. Thus, the sulphur and lead deposited in the studied ore veins were probably leached from Triassic metabasic and metaclastic rocks some time during the Early Cretaceous to the Palaeocene.     

Geology,geochronology, and Hf isotope geochemistry of the Longtougang skarn and hydrothermal vein Cu–Zn deposit,North Wuyi area,southeastern China

The recently discovered Longtougang skarn and hydrothermal vein Cu–Zn deposit is located in the North Wuyi area, southeastern China. The intrusions in the ore district comprise several small porphyritic biotite monzonite, porphyritic monzonite, and porphyritic granite plutons and dikes. The mineralization is zoned from a lower zone of Cu-rich veins and Cu–Zn skarns to an upper zone of banded Zn–Pb mineralization in massive epidote altered rocks. The deposit is associated with skarn, potassic, epidote, greisen, siliceous, and carbonate alteration. Molybdenite from the Cu-rich veins yielded a Re–Os isochron age of 153.6 ± 3.9 Ma, which is consistent with U–Pb zircon ages of 154.0 ± 1.3 Ma for porphyritic monzonite, 154.0 ± 0.8 Ma for porphyritic biotite monzonite, and 152.0 ± 0.8 Ma for porphyritic granite. Geological observations suggest that the Cu mineralization is genetically related to the porphyritic biotite monzonite and porphyritic monzonite. All the zircons from intrusive rocks in the ore district are characterized by ε_Hf(t) values between − 13.41 and − 4.38 and Hf model ages (T_DM2) between 2054 and 1482 Ma, reflecting magmas derived mainly from a Proterozoic crustal source. Molybdenite grains from the deposit have Re values of 14.6–27.7 ppm, indicative of a mixed mantle–crust source. The porphyry–skarn abundant Cu and hydrothermal vein type Pb–Zn–Ag deposits in the North Wuyi area are related to the Late Jurassic porphyritic granites and Early Cretaceous volcanism, respectively. The Late Jurassic mineralization-related granites were derived from the crustal anatexis with some mantle input, which was triggered by asthenospheric upwelling induced by slab tearing during oblique subduction of the paleo-Pacific plate beneath the South China block, and the Early Cretaceous mineralization-related granitoids mainly from crust material formed within a series of NNE-trending basins during margin-parallel movement of the plate.     

Characteristics and origin of ore-forming fluids of Jinchangqing gold （copper） ore deposit （s） in Xiangyun, Yunnan Province

On the basis of results of the studies of primary fluid inclusions, and the hydrogen and oxygen isotope data, the authors concluded that the early-stage ore-forming fluid from the Jinchangqing gold(copper) ore deposit is a kind of sulfate type hot brine characterized by medium temperature and salinity,genetically related to the late-stage ore-forming fluid derived from an acidic and more reduetive environment. However, the late-stage ore-forming fluid is a sort of low temperature and low salinity chloride-type hot brine which originated from a lower pressure, acidic and more oxidative environment. In general, the ore fluids were derived from the late-stage, or largely from the early-stage groundwater-derived meteoric water, which has a 12‰-17‰ heavier oxygen isotopic composition than the original rain water (δ^18O=- 15.3‰), and were formed during gold mineralization as a product of oxygen isotope exchange during the reaction between ore-forming fluid and wall rocks under a lower water/rock ratio condition.