Shear modulus, heat capacity, viscosity and structural relaxation time of Na2O–Al2O3–SiO2 and Na2O–Fe2O3–Al2O3–SiO2 melts

The configurational heat capacity, shear modulus and shear viscosity of a series of Na₂O–Fe₂O₃–Al₂O₃–SiO₂ melts have been determined as a function of composition. A change in composition dependence of each of the physical properties is observed as Na₂O/(Na₂O + Al₂O₃) is decreased, and the peralkaline melts become peraluminous and a new charge-balanced Al-structure appears in the melts. Of special interest are the frequency dependent (1 mHz–1 Hz) measurements of the shear modulus. These forced oscillation measurements determine the lifetimes of Si–O bonds and Na–O bonds in the melt. The lifetime of the Al–O bonds could not, however, be resolved from the mechanical spectrum. Therefore, it appears that the lifetime of Al–O bonds in these melts is similar to that of Si–O bonds with the Al–O relaxation peak being subsumed by the Si–O relaxation peak. The appearance of a new Al-structure in the peraluminous melts also cannot be resolved from the mechanical spectra, although a change in elastic shear modulus is determined as a function of composition. The structural shear-relaxation time of some of these melts is not that which is predicted by the Maxwell equation, but up to 1.5 orders of magnitude faster. Although the configurational heat capacity, density and shear modulus of the melts show a change in trend as a function of composition at the boundary between peralkaline and peraluminous, the deviation in relaxation time from the Maxwell equation occurs in the peralkaline regime. The measured relaxation times for both the very peralkaline melts and the peraluminous melts are identical with the calculated Maxwell relaxation time. As the Maxwell equation was created to describe the timescale of flow of a mono-structure material, a deviation from the prediction would indicate that the structure of the melt is too complex to be described by this simple flow equation. One possibility is that Al-rich channels form and then disappear with decreasing Si/Al, and that the flow is dominated by the lifetime of Si–O bonds in the Al-poor peralkaline melts, and by the lifetime of Al–O bonds in the relatively Si-poor peralkaline and peraluminous melts with a complex flow mechanism occurring in the mid-compositions. This anomalous deviation from the calculated relaxation time appears to be independent of the change in structure expected to occur at the peralkaline/peraluminous boundary due to the lack of charge-balancing cations for the Al-tetrahedra.     

The molar volume of FeO–MgO–Fe2O3–Cr2O3–Al2O3–TiO2 spinels

We define and calibrate a new model of molar volume as a function of pressure, temperature, ordering state, and composition for spinels in the supersystem (Mg, Fe²⁺)(Al, Cr, Fe³⁺)₂O₄ ? (Mg, Fe²⁺)₂TiO₄. We use 832 X-ray and neutron diffraction measurements performed on spinels at ambient and in situ high-P, T conditions to calibrate end-member equations of state and an excess volume model for this system. The effect on molar volume of cation ordering over the octahedral and tetrahedral sites is captured with linear dependence on Mg²⁺, Al³⁺, and Fe³⁺ site occupancy terms. We allow standard-state volumes and coefficients of thermal expansion of the end members to vary within their uncertainties during extraction of the mixing properties, in order to achieve the best fit. Published equations of state of the various spinel end members are analyzed to obtain optimal values of the bulk modulus and its pressure derivative, for each explicit end member. For any spinel composition in the supersystem, the model molar volume is obtained by adding excess volume and cation order-dependent terms to a linear combination of the five end-member volumes, estimated at pressure and temperature using the high-T Vinet equation of state. The preferred model has a total of 9 excess volume and order-dependent parameters and fits nearly all experiments to within 0.02 J/bar/mol, or better than 0.5 % in volume. The model is compared to the current MELTS spinel model with a demonstration of the impact of the model difference on the estimated spinel-garnet lherzolite transition pressure.     

Origin of the Maoduan Pb–Zn–Mo deposit, eastern Cathaysia Block, China: geological, geochronological, geochemical, and Sr–Nd–Pb–S isotopic constraints

The Maoduan Pb–Zn–Mo deposit is in hydrothermal veins with a pyrrhotite stage followed by a molybdenite and base metal stage. The Re–Os model ages of five molybdenite samples range from 138.6 ± 2.0 to 140.0 ± 1.9 Ma. Their isochron age is 137.7 ± 2.7 Ma. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) zircon U–Pb dating of the nearby exposed Linggen granite porphyry gave a ²⁰⁶Pb/²³⁸U age of 152.2 ± 2.2 Ma and the hidden Maoduan monzogranite yielded a mean of 140.0 ± 1.6 Ma. These results suggest that the intrusion of the Maoduan monzogranite and Pb–Zn–Mo mineralization are contemporaneous. δ ³⁴S values of sulfide minerals range from 3.4‰ to 4.8‰, similar to magmatic sulfur. Four sulfide samples have ²⁰⁶Pb/²⁰⁴Pb = 18.252–18.432, ²⁰⁷Pb/²⁰⁴Pb = 15.609–15.779, and ²⁰⁸Pb/²⁰⁴Pb = 38.640–39.431, similar to the age-corrected data of the Maoduan monzogranite. These isotope data support a genetic relationship between the Pb–Zn–Mo mineralization and the Maoduan monzogranite and probably indicate a common deep source. The Maoduan monzogranite has geochemical features similar to highly fractionated I-type granites, such as high SiO₂ (73.7–75.2 wt.%) and alkalis (K₂O + Na₂O = 7.8–8.9 wt.%) and low FeO_t (0.8–1.3 wt.%), MgO (~0.3 wt.%), P₂O₅ (~0.03 wt.%), and TiO₂ (~0.2 wt.%). The granitic rocks are enriched in Rb, Th, and U but depleted in Ba, Sr, Nb, Ta, P, and Ti. REE patterns are characterized by marked negative Eu anomalies (Eu/Eu^* = 0.2–0.4). The Maoduan monzogranite, having (⁸⁷Sr/⁸⁶Sr) _t  = 0.7169 to 0.7170 and ε_Nd(t) = −13.8 to −13.7, was probably derived from mixing of partial melts from enriched mantle and the Paleoproterozoic Badu group in an extensional tectonic setting.     

Hydrogen incorporation into forsterite in Mg2SiO4–K2Mg(CO3)2–H2O and Mg2SiO4–H2O–C at 7.5–14.0 GPa

Experiments on water solubility in forsterite in the systems Mg₂SiO₄–K₂Mg(CO₃)₂–H₂O and Mg₂SiO₄–H₂O–C were conducted at 7.5–14.0 GPa and 1200–1600 °C. The resulting crystals contain 448 to 1480 ppm water, which is 40–70% less than in the forsterite–water system under the same conditions. This can be attributed to lower water activity in the carbonate-bearing melt. The water content of forsterite was found to vary systematically with temperature and pressure. For instance, at 14 GPa in the system forsterite–carbonate–H₂O the H₂O content of forsterite drops from 1140 ppm at 1200 °C to 450 ppm at 1600 °C, and at 8 GPa it remains constant or increases from 550 to 870 ppm at 1300–1600 °C. Preliminary data for D-H-bearing forsterite are reported. Considerable differences were found between IR spectra of D-H- and H-bearing forsterite. The results suggest that CO₂ can significantly affect the width of the olivine-wadsleyite transition, i.e., the 410-km seismic discontinuity, which is a function of the water content of olivine and wadsleyite.     

Hydrogen incorporation in enstatite in the system MgO–SiO2–H2O–NaCl

The incorporation of hydrogen in enstatite in a hydrous system containing various amounts of NaCl was investigated at 25 kbar. The hydrogen content in enstatite shows a clear negative correlation to the NaCl-concentration in the system. The most favourable explanation is the reduction of water fugacity due to dilution. Other reasons for the limited hydrogen incorporation at high NaCl levels, such as a significant influence of Na⁺ on the defect chemistry or an exchange between OH^- and Cl⁻in enstatite, appear much less important. A partition coefficient D _Na ^En/Fluid = 0.0013 could be determined, demonstrating that Na is less incompatible in enstatite than H. The new results support the idea that dissolved components have to be considered when the total hydrogen storage capacity in nominally anhydrous minerals is estimated, especially in geological settings with high levels of halogens, such as subduction zones.     

The Transfiguration continental red-bed Cu–Pb–Zn–Ag deposit,Quebec Appalachians,Canada

The Transfiguration Cu–Pb–Zn–Ag deposit, enclosed within reduced grey sandstone, is associated with continental red beds of the Lower Silurian Robitaille Formation in the Quebec Appalachians, Canada. The Robitaille Formation rests unconformably on foliated Cambro-Ordovician rocks. The unconformity is locally cut by barite veins. The basal unit of the Robitaille Formation comprises green wacke and pebble conglomerate, which locally contain calcite nodules. The latter have microstructures characteristic of alpha-type calcretes, such as “floating” fabrics, calcite-filled fractures (crystallaria) and circumgranular cracks. Massive, grey sandstone overlies the basal green wacke and pebble conglomerate unit, which is overlain, in turn, by red, fine-grained sandstone. Mineralisation occurred underneath the red sandstone unit, chiefly in the grey sandstone unit, as disseminated and veinlet sulphides. Chalcopyrite, the most abundant Cu sulphide, replaced early pyrite. Calcrete, disseminated carbonate and vein carbonate have stable isotope ratios varying from −7.5‰ to −1.1‰ δ¹³C and from 14.7‰ to 21.3‰ δ¹⁸O. The negative δ¹³C values indicate the oxidation of organic matter in a continental environment. Sulphur isotope ratios for pyrite, chalcopyrite and galena vary from −19‰ to 25‰ δ³⁴S, as measured on mineral concentrates by a conventional SO₂ technique. Laser-assisted microanalyses (by fluorination) of S isotopes in pyrite show an analogous range in δ³⁴S values, from −21‰ to 25‰. Negative and positive δ³⁴S values are compatible with bacterial sulphate reduction (BSR) in systems open and closed with respect to sulphate. We interpret similarly high δ³⁴S values for sulphide concentrates (25.1‰) and for vein barite (26.2‰) to result from rapid and complete thermochemical reduction of pore-water sulphate. Two early to late diagenetic stages of mineralisation best explain the origin of the Transfiguration deposit. The first stage was characterised by the ponding of groundwater over the Taconian unconformity, recorded by calcrete and early pyrite formation via BSR in grey sandstone. Early pyrite contains up to 2 wt.% Pb, which is consistent with Pb fixation by sulphate-reducing bacteria. The second stage (II) is defined by the replacement of early pyrite by chalcopyrite, as well as by sulphide precipitation via either BSR or thermochemical sulphate reduction (TSR) in grey sandstone. This event resulted from the synsedimentary fault-controlled percolation and mixing of (1) an oxidising, sulphate-bearing cupriferous fluid migrating per descensum from the red-bed sequence and (2) a hydrocarbon-bearing fluid migrating per ascensum from the Cambro-Ordovician basement. Mixing between the two fluids led to sulphate reduction, causing Cu sulphide precipitation. The positive correlation between Cu and Fe³⁺/Fe²⁺ bulk rock values suggests that Fe acted as a redox agent during sulphate reduction. Stage II diagenetic fluid migration is tentatively attributed to the Late Silurian Salinic extensional event.     

Multi-stage Ag–Bi–Co–Ni–U and Cu–Bi vein mineralization at Wittichen,Schwarzwald, SW Germany: geological setting,ore mineralogy,and fluid evolution

The Wittichen Co–Ag–Bi–U mining area (Schwarzwald ore district, SW Germany) hosts several unconformity-related vein-type mineralizations within Variscan leucogranite and Permian to Triassic redbeds. The multistage mineralization formed at the intersection of two fault systems in the last 250 Ma. A Permo-Triassic ore stage I with minor U–Bi–quartz–fluorite mineralization is followed by a Jurassic to Cretaceous ore stage II with the main Ag and Co mineralization consisting of several generations of gangue minerals that host the sub-stages of U–Bi, Bi–Ag, Ni–As–Bi and Co–As–Bi. Important ore minerals are native elements, Co and Ni arsenides, and pitchblende; sulphides are absent. The Miocene ore stage III comprises barite with the Cu–Bi sulfosalts emplectite, wittichenite and aikinite, and the sulphides anilite and djurleite besides native Bi, chalcopyrite, sphalerite, galena and tennantite. The mineral-forming fluid system changed from low salinity (<5 wt.% NaCl) at high temperature (around 300°C) in Permian to highly saline (around 25 wt.% NaCl + CaCl₂) at lower temperatures (50–150°C) in Triassic to Cretaceous times. Thermodynamic calculations and comparison with similar mineralizations worldwide show that the Mesozoic ore-forming fluid was alkaline with redox conditions above the hematite–magnetite buffer. We suggest that the precipitation mechanism for native elements, pitchblende and arsenides is a decrease in pH during fluid mixing processes. REE patterns in fluorite and the occurrence of Bi in all stages suggest a granitic source of some ore-forming elements, whereas, e.g. Ag, Co and Ni probably have been leached from the redbeds. The greater importance of Cu and isotope data indicates that the Miocene ore stage III is more influenced by fluids from the overlying redbeds and limestones than the earlier mineralization stages.     

Genesis of the Angeer Yinwula Pb–Zn deposit,Inner Mongolia,China: constraints from fluid inclusions,C–H–O–S–Pb isotope systematics,and zircon U–Pb geochronology

Arabian Journal of Geosciences - Soil toxic metal pollution is one of the most prominent environmental problems in the rapid industrialization of societies because of the considerable harm caused...     

An improved cubic model for the mutual solubilities of CO2–CH4–H2S–brine systems to high temperature,pressure and salinity

The phase behavior of CO₂–CH₄–H₂S–brine systems is of importance for geological storage of greenhouse gases, sour gas disposal and enhanced oil recovery (EOR). In such projects, reservoir simulations play a major role in assisting decision makings, while modeling the phase behavior of the relevant CO₂–CH₄–H₂S–brine system is a key part of the simulation. There is a need for an equation of state (EOS) for such system which is accurate, with wide application range (pressure, temperature and aqueous salinity), computationally efficient and easy for implementation in a reservoir simulator.In this study, an improved cubic EOS model of the system CO₂–CH₄–H₂S–brine is developed based on the modifications of the binary interaction parameters in Peng–Robinson EOS, which is widely implemented in reservoir simulators. Thus the new model is suited for numerical implementation in reservoir simulators.The available experimental data of pure gas brine equilibrium and gas mixture solubility in water/brine are carefully reviewed and compared with the new model. From the comparison, the new model can accurately reproduce (1) the CO₂–brine mutual solubility data at temperature from 0 °C to 250 °C, pressure from 1 bar to 1000 bar and NaCl molality (mole number in 1 kg water, molal is used for short) from 0 to 6 molal, (2) CH₄–brine mutual solubility data at temperature from 0 °C to 250 °C, pressure from 1 bar to 2000 bar and NaCl molality from 0 to 6 molal, (3) H₂S–brine mutual solubility data at temperature from 0 °C to 250 °C, pressure from 1 bar to 200 bar and NaCl molality from 0 to 6 molal, and (4) has good accuracy for gas mixture solubility in brine.     

Platinum Mineralization in Multimetal Gold–Polymetallic,Au–Bi,Cu–Mo Porphyry,Cu–Ni,Titanomagnetite, and Copper–Sulfide Ore Deposits and Occurrences of the Upper Amur Region (Far East,Russia)

New data on platinum mineralization in ores, metasomatic rocks, concentrates, and tailings and wastes of some gold–polymetallic, Au–Bi, Cu–Mo porphyry, Cu–Ni, and titanomagnetite ore deposits and occurrences of the Upper Amur Region are presented. The contents of platinoids, Au and Ag in multimetal ores of gold-polymetallic, Au–Bi, Cu–Mo porphyry, Cu–Ni, and titanomagnetite ore deposits and ore occurrences are given. In addition, recommendations on the necessity of continuing scientific studies, revision, and resampling works in the search for platinoids in other complex ores of deposits and occurrences of the Upper Amur Region are given.     

As–Sb–Bi–Au mineralization in the Baogutu gold deposit,Xinjiang, NW China

Here we report the occurrence of some uncommon mineral assemblages including pääkönenite, aurostibite, native arsenic, native antimony, and native bismuth found in the Baogutu gold deposit in the western Junggar, Xinjiang, NW China. The mineralization could be generally subdivided into two types: the gold-bearing quartz-vein type mineralization and disseminated mineralization in the wall rocks. The sulfide minerals in gold lodes commonly include pyrite, arsenopyrite, marcasite, and stibnite. However, the L7 lode in No. 4 orebody and the L1 lode in No. 11 orebody of the Baogutu gold deposit are quite different in terms of their mineral assemblages. The L7 lode contains native arsenic–quartz veins in shallow levels and stibnite–quartz veins at depth. Gold-bearing minerals (electrum, native gold, and rarely aurostibite) mainly coexist with pääkönenite, stibnite, native arsenic, and native antimony. The crystallization of As- and Sb-bearing minerals was likely to have consumed H₂S from the hydrothermal fluid, which probably triggered the precipitation of native gold. The L1 lode consists of several discontinuous sulfide-dominated lensoid orebodies. The massive sulfide ores that produced most of the gold resource are characterized by an intimate association between native bismuth and native gold mineralization.     

Molybdenite Re–Os,zircon U–Pb dating and Hf isotopic analysis of the Shuangqing Fe–Pb–Zn–Cu skarn deposit,East Kunlun Mountains,Qinghai Province,China

The Shuangqing Fe–Pb–Zn–Cu deposit is located in the Xiangride County of Qinghai Province, China, and is a typical example of skarn deposits in the East Kunlun Mountains. Skarnization and mineralization took place along the contact zone between Carboniferous carbonates and the concealed Triassic plagiogranite. LA–ICP–MS U–Pb dating of zircons from the plagiogranite has yielded ages of 227.2 ± 1.0 and 226.54 ± 0.97 Ma, which are interpreted as the emplacement age of the plagiogranite. Molybdenites separated from ore-bearing quartz-veins yielded a Re–Os isochron age of 226.5 ± 5.1 Ma. These age data confirm that both intrusion and related skarn mineralization initiated at ~ 227 Ma. Re contents of molybdenite, zircon ε_Hf(t) and ¹⁷⁶Hf/¹⁷⁷Hf values fall into the ranges 3.31 to 6.58 μg/g, − 8.6 to − 0.0, and 0.282403 to 0.28263850, respectively. The timing of the Shuangqing Fe–Pb–Zn–Cu mineralization coincided with a major change in the stress field in East Kunlun from transpression to extension, related to the partial melting of thickening crustal materials in a post-collisional tectonic setting.     

Origin of the Tongshankou porphyry–skarn Cu–Mo deposit,eastern Yangtze craton,Eastern China: geochronological,geochemical, and Sr–Nd–Hf isotopic constraints

The Tongshankou Cu–Mo deposit, located in the westernmost Daye district of the Late Mesozoic Metallogenic Belt along the Middle-Lower reaches of the Yangtze River, eastern China, consists mainly of porphyry and skarn ores hosted in the Tongshankou granodiorite and along the contact with the Lower Triassic marine carbonates, respectively. Sensitive high-resolution ion microprobe zircon U–Pb dating constrains the crystallization of the granodiorite at 140.6 ± 2.4 Ma (1σ). Six molybdenite samples from the porphyry ores yield Re–Os isochron age of 143.8 ± 2.6 Ma (2σ), while a phlogopite sample from the skarn ores yields an ⁴⁰Ar/³⁹Ar plateau age of 143.0 ± 0.3 Ma and an isochron age of 143.8 ± 0.8 Ma (2σ), indicating an earliest Cretaceous mineralization event. The Tongshankou granodiorite has geochemical features resembling slab-derived adakites, such as high Sr (740–1,300 ppm) and enrichment in light rare earth elements (REE), low Sc (<10 ppm), Y (<13.3 ppm), and depletion in heavy REE (<1.2 ppm Yb), and resultant high Sr/Y (60–92) and La/Yb (26–75) ratios. However, they differ from typical subduction-related adakites by high K, low MgO and Mg#, and radiogenic Sr–Nd–Hf isotopic compositions, with (⁸⁷Sr/⁸⁶Sr) _t  = 0.7062–0.7067, ɛ _Nd(t) = −4.37 to −4.63, (¹⁷⁶Hf/¹⁷⁷Hf) _t  = 0.282469–0.282590, and ɛ _Hf(t) = −3.3 to −7.6. The geochemical and isotopic data, coupled with geological analysis, indicate that the Tongshankou granodiorite was most likely generated by partial melting of enriched lithospheric mantle that was previously metasomitized by slab melts related to an ancient subduction system. Magmas derived from such a source could have acquired a high oxidation state, as indicated by the assemblage of quartz–magnetite–titanite–amphibole–Mg-rich biotite in the Tongshankou granodiorite and the compositions of magmatic biotite that fall in the field between the NiNiO and magnetite–hematite buffers in the Fe³⁺–Fe²⁺–Mg diagram. Sulfur would have been present as sulfates in such highly oxidized magmas, so that chalcophile elements Cu and Mo were retained as incompatible elements in the melt, contributing to subsequent mineralization. A compilation of existing data reveals that porphyry and porphyry-related Cu–Fe–Au–Mo mineralization from Daye and other districts of the Metallogenic Belt along the Middle-Lower reaches of the Yangtze River took place coevally in the Early Cretaceous and was related to an intracontinental extensional environment, distinctly different from the arc-compressive setting of the Cenozoic age that has been responsible for the emplacement of most porphyry Cu deposits of the Pacific Rim.     

Shallow submarine epithermal Pb–Zn–Cu–Au–Ag–Te mineralization on western Milos Island,Aegean Volcanic Arc,Greece: Mineralogical,geological and geochemical constraints

Milos Island contains several epithermal deposits (e.g., Profitis Ilias–Chondro Vouno Pb–Zn–Ag–Au–Te–Cu, Triades–Galana–Agathia–Kondaros Pb–Zn–Ag–Bi–W–Mo ± Cu–Au, and Katsimoutis–Kondaros–Vani Pb–Zn–Ag–Mn) of Late Pliocene to Early Pleistocene age. These deposits are hosted in calc-alkaline volcanic rocks emplaced as a result of three successive magma pulses in an emergent volcanic edifice: submarine rhyolitic to rhyodacitic cryptodomes at ca. 2.7. Ma (Profitis Ilias–Chondro Vouno), submarine to subaerial andesite to dacite domes at ca. 2.2 to 1.5 Ma (Triades–Galana–Kondaros–Katsimouti–Vani). Hydrothermal alteration of the volcanic rocks includes advanced argillic- (both hypogene and steam-heated), argillic, phyllic, adularia-sericite and propylitic types. In the northern sector (Triades–Galana–Agathia–Kondaros), initial magma degassing derived from andesitic–dacitic intrusives along NE–SW to E–W trending faults resulted in the development of pre-ore hypogene advanced argillic alteration (dickite, alunite, ± diaspore, pyrophyllite, halite, and pyrite) in a submarine environment. Mineralogical data indicate common features among the Profitis Ilias–Chondro Vouno, Kondaros–Katsimoutis–Vani and Triades–Galana mineralized centers, all of which are characterized by the presence of galena, Fe-poor sphalerite, and chalcopyrite as well as abundant barite, adularia, sericite and, to a lesser extent, calcite, which are typical of intermediate-sulfidation epithermal type deposits. Locally, at Triades–Galana and Kondaros–Agathia, high-sulfidation conditions prevailed as suggested by the presence of coexisting enargite and covellite. The high silver and gold content of the western Milos deposits is derived from Ag-bearing sulfosalts (polybasite, pearceite, pyrargyrite, freibergite) and tellurides. Gold at Profitis Ilias, both as native gold and silver-gold tellurides, is present in base-metal precipitates within multicomponent blebs, which recrystallized to form hessite, petzite, altaite, coloradoite, and native gold. Mineralogical evidence (e.g. microchimney structures, copper sulfides, widespread occurrence of barite, aragonite) suggests that precious metal mineralization in western Milos mineralization formed in a submarine setting.We present information on the surface distribution of Au, Ag, Cu, Pb, Zn, As, Sb, Hg, Mo, Bi, W and Cd at western Milos. Gold is enriched at Profitis Ilias–Chondro Vouno deposits and to a lesser extent at Triades–Galana. Arsenic is absent from the southern sector but shows elevated concentrations together with molybdenum, bismuth and tungsten at the northern sector (Triades–Galana, Vani deposits). The differences in precious and base metal abundances may be related to the depths at which the deposits are exposed, and/or different sources of magma. The metal signatures of the Triades–Galana and Agathia–Kondaros–Katsimouti–Vani (Mo–Bi–W–As–Hg–Ag–Au) occurrences compared to Profitis Ilias (Te–Au–Ag) reflect different sources of magma (dacite–rhyodacite for Profitis Ilias, andesite–dacite for Triades–Galana, and dacite for Kondaros–Katsimoutis). The enrichment of Te, Mo, W, and Bi in the deposits is a strong indication of a direct magmatic contribution of these metals.At western Milos, precious and base-metal vein mineralization was deposited during episodic injection of magmatic volatiles and dilution of the hydrothermal fluids by seawater. The mineralization represents seafloor/sub-seafloor precipitation of sulfides that formed in stockwork zones. Base and precious metal mineralization formed from intermediate- to high-sulfidation state fluids and mostly under boiling conditions as indicated by the widespread occurrence of adularia associated with metallic mineralization. We speculate that the widespread occurrence of boiling and the shallow depth of the precious- and base-metal emplacement prevented the formation of seafloor massive sulfides.     

Platinum–palladium–gold mineralization in the Nkenja mafic–ultramafic body, Ubendian metamorphic belt, Tanzania

Significant and widespread enrichment of platinum, palladium, and gold has been found within the Nkenja mafic–ultramafic body located in southern Tanzania in the central part of the Ubendian metamorphic belt. This body is dominated by partly serpentinized chromitiferous dunite, wehrlite and olivine clinopyroxenite, which are tectonically intercalated with amphibolitized metagabbro. The dunites contain both disseminated and seam-type chrome spinel with an Al-rich composition. The seams are thin, impersistent and, together with enclosing dunite, often show deformation at granulite facies conditions. Forsterite contents of olivine in the dunite range from 87 to 92?mol%. Clinopyroxene in wehrlite and clinopyroxenite is diopsidic with significant contents of Al and Na. Clinopyroxene forms irregular bands and crosscutting veins in the dunite, as well as occurring as weakly dispersed isolated grains in the dunite. Elevated levels of Pt, Pd and Au occur in all ultramafic rocks, but not amphibolitized metagabbro, and there is a weak correlation between high abundances of platinum-group element (PGE) and chromitites. PGE values are erratically distributed and are associated with trace to minor amounts of disseminated sulphides (pyrrhotite, pentlandite, heazlewoodite, chalcopyrite and bornite). The abundances of all PGE are consistently anomalous, suggesting a primary igneous control by sulphides in ultramafic rock. However, there has evidently been a strong metamorphic and/or hydrothermal overprint on what was probably an original magmatic concentration of PGE-bearing sulphides. Geological mapping and petrological evidence, as well as the style of PGE sulphide mineralization, are consistent with the Nkenja ultramafic body being part of the crustal section of a dismembered Palaeoproterozoic ophiolite.     

Discovery of Lorandite TlAsS2 at the Distal Au–Tl Deposit in a Skarn system, Fengshan Area, Middle–Lower Yangtze River, Eastern China

<正>Objective Thallium has been used as an indicator element in geochemical exploration of searching for hydrothermal gold deposits.However,the T1 minerals and mineralization are rare in nature.Lorandite TlAsS_2,a relatively uncommon mineral,has been dominantly discovered in some Carlin gold deposits,and minor SbHg,U and Pb-Zn-Ag deposits.It is of a hydrothermal origin and was typically formed at relatively low temperatures.The relationships between these deposits containing lorandite and intrusions remain a highly