High Concentrations Of Au Research Articles

Genesis of the Sanhetun Tellurium–Gold Deposit, Northeast China: Constraints from In Situ Elemental and Sulfur Isotopic Compositions of Pyrite

The Sanhetun tellurium–gold (Te–Au) deposit, located in the Duobaoshan polymetallic metallogenic belt (DPMB) within the eastern section of the Central Asian Orogenic Belt (CAOB), is a newly discovered small-scale gold deposit. The mineralization, with a resource of ≥4 t Au, is mainly hosted in three NNE-trending alteration zones between Early Carboniferous granitic mylonite and Lower Cretaceous volcanogenic-sedimentary formations. The genesis of formation of this deposit is poorly constrained. Here, we report the results of petrographic studies, TESCAN Integrated Mineral Analyzer (TIMA), major and trace element concentrations, and in situ S isotopes of pyrite. The results show that there are four types of pyrite: coarse-grained euhedral Py1, fine-grained quartz-Py2 vein crosscutting Py1, anhedral aggregated Py3, and anhedral aggregated Py4. The pre-ore stage Py1 contains negligible Au, Te, and other trace elements and has a relatively narrow range of δ34S values ranging from −1.20 to −0.57‰. Py2 has higher concentrations of Au and Te and distinctly high concentrations of Mo, Sb, Zn, and Mn with markedly positive δ34S values of 4.67 to 14.43‰. The main-ore stage Py3 contains high Au and Te concentrations and shows narrow δ34S values ranging from −5.69 to 0.19‰. The post-ore stage Py4 displays low Au concentrations with the δ34S values ranging from 2.66 to 3.86‰. Tellurides are widespread in Py3 and Py4, consisting mainly of native tellurium, tetradymite, tsumoite, hessite, and petzite. Especially, tetradymite commonly coexists with native gold. This study highlights the role of Te–Bi–S melt as an important gold scavenger in As-deficient ore-forming fluids.

Petrogenesis and tectonic evolution of mineralized mafic intrusions in the Eastern Desert of Egypt: Implications for gold–sulfide genesis

The whole–rock chemistry, mineral chemistry, and remote sensing data of the Atud–UmKhasila Neoproterozoic mafic intrusions in the Eastern Desert of Egypt show two different mafic plutons: (1) the metagabbro–diorite complex; and (2) the G. Atud gabbros. Both of these contain two types of Cu–Ni–Fe–sulfide mineralizations. Multispectral remotely sensed images of Landsat 8 OLI/TIRS, Sentinel 2–B, and ASTER1T were used to give an overview of hydrothermal alteration signatures and distinguish different lithological units. The G. Atud gabbros are intruded into the metagabbro–diorite complex and consist mainly of olivine gabbros, while the metagabbro–diorite complex comprises metagabbros, diorites, and quartz diorites. They were formed under high fO2 (ΔFMQ= +1.43 to + 0.33) with a higher crystallization temperature (∼ 900–1100 °C) and pressure (∼ 6.0 kbar on average) at 18 km depth relative to associated metagabbros. Like magmatic sulfides in mafic intrusions, the G. Atud gabbros contain disseminated grains of pyrrhotite, pentlandite, chalcopyrite, and pyrite, up to 5 vol%. On the other hand, sulfide deposits (up to 30 vol%) such as pyrite, As–bearing pyrite, arsenopyrite, and gold with minor sphalerite and galena at the Atud gold mine, are related to the metagabbro–diorite intrusion. They are found as disseminations, patches, microveinlets, and bands. The sulfide deposits and economic gold are spatially concentrated in smoky quartz veins (up to 25 g/t) and metasomatic alteration zones, i.e., silicification and hematization of metagabbros (0.32 g/t), phyllic, argillic, and propylitic alteration, and carbonate–silicified zones, along gabbroic intrusive contacts, which all follow the Najd NW–SE shear zone. They are possibly of hydrothermal origin (epigenetic). They are also precipitated by mineralized fluids (rich in Si, K, Fe, Pb, Ag, Au, As, S, Ni, Zn, Cu, CO2, and H2O) that have been derived from a mixed magmatic–metamorphic source. The high Au contents with As–bearing pyrite and arsenopyrite in both Fe–rich and smoky quartz veins are related to the interaction between Fe from metagabbro–diorites and the Au(HS)-2 compound as well as the crystallization of pyrite, which reduced the sulfur contents in the mineralized fluids and hence led to gold precipitation. The late intrusion of G. Atud gabbros into metagabbro–diorite rocks enhanced the circulation of sulfide-gold-bearing hydrothermal fluids towards the contacts of the latter ones. These fluids along the shear zones cause metasomatic alteration in addition to leaching and the collection of sulfides and gold in the metagabbros. The protoliths of metagabbro–diorite rocks have a calc–alkaline nature and were formed in a volcanic arc setting, while the G. Atud gabbros were crystallized from Mg-rich tholeiitic melts in the extensional rift (e.g., rifted arc) setting as a result of asthenospheric upwelling due to the slab detachment and/or lithospheric delamination. The Atud gold–sulfide mineralization was related to the thermal uplifting–extensional tectonism. The enrichment of the G. Atud gabbros in LILE, alongside LREE over HFSE, reflects their derivation from a metasomatized mantle source during a rifted arc following the subduction processes.

Genesis of the Kateba’asu gold deposit, Western Tianshan, China: Constraints from pyrite trace element, sulfur isotope, and quartz H-O isotopes

The Kateba’asu gold deposit, situated in the Western Tianshan of China, is one of the most significant discoveries in the world-class Tianshan gold belt. The deposit features two distinct mineralization styles. The early, subordinate skarn-type copper–gold mineralization occurs in the contact zone between monzogranite, diorite, and Silurian limestone, composed of garnet, diopside, epidote, chalcopyrite, pyrite, and gold. The later, primary lode-gold mineralization is hosted in the altered monzogranite characterized by pervasive quartz-pyrite-sericite-chlorite-K-feldspar alteration and a well-develped veining systems.Pyrite is the dominant sulfide mineral related to gold mineralization in the Kateba’asu gold deposit, with four types identified: Py0 from the early skarn copper–gold mineralization, and Py1 to Py3 from the later lode-gold mineralization. All types of pyrite are homogeneous and contain very low levels of lattice-bound gold. Py0 is euhedral and fine-grained, with relatively high Cu, Au, Co, and Ni contents, and displays a magmatic sulfur isotopic signature with δ34S ranging from 0.8 to 4.3 ‰. Py1 occurs as euhedral to subhedral, coarse-grained crystals within pyrite-quartz veins with higher concentrations of Co and Ni. Py2, which develops in the quartz-pyrite veins, is medium to coarse-grained and contains elevated levels of As, Cu, Zn, and Bi relative to Py1. Py3, found in polymetallic sulfide veins of the main lode-gold stage, is anhedral and medium to fine-grained with higher contents of As, Ag, Cu, Zn, Se, Te and lowest Co and Ni concentrations compared to Py1 and Py2. The positive correlations between Au-Te, Au-Bi, Au-Cu, and Pb-Bi across all pyrite types, along with the presence of visible gold in Py3, indicate that most gold occurs as micro-/nano-sized inclusions and as fissure gold. The δ34S values of Py1, Py2, and Py3 (7.6 to 11.8 ‰, 10.1 to 12.6 ‰, and 9.8 to 12.4 ‰, respectively) were attributed to an initial magmatic source and mixed with external sulfur subsequently from the wall rocks. The H and O isotopic compositions (δDH2O = −84.1 to −93.5 ‰; δ18OH2O = 1.8 to 6.6 ‰) of quartz from the lode-gold mineralization imply that ore-forming fluids were predominantly of magmatic origin, with a additional contribution from meteoric water. Taken together, a two-episode mineralization model was proposed for the formation of the Kateba’asu gold deposit. The early skarn mineralization stage is associated with the emplacement of diorite during the Early Carboniferous. In contrast, the subsequent lode-gold mineralization, occurring between the Late Carboniferous and Permian periods, represents a overprinted magmatic-hydrothermal gold system potentially linked to a deep-seated magmatic intrusion.

Machine learning based prospect targeting: A case of gold occurrence in central parts of Tanzania, East Africa

Soil geochemical analyses from central Tanzania reveal significant gold (Au) values, highlighting the potential for further exploration in the region. This study employs ensemble machine learning models—XGBoost-RF, XGBoost-SVM, and XGBoost-ANN—to enhance predictions of Au distribution. Among these, the XGBoost-ANN model showed the highest accuracy during the training phase, achieving a Mean Absolute Percentage Error (MAPE) of 1.275, a Root Mean Square Error (RMSE) of 0.031, an R² of 0.999, and a Pearson Correlation Coefficient (PCC) of 0.999. However, its performance declined in the testing phase with a MAPE of 0.0668 and an RMSE of 0.2491, indicating reduced predictiveness on new data. Spatial analyses using Global and Local Moran's I tests revealed no significant global spatial autocorrelation but identified localized clusters of high and low Au concentrations. Specific areas showed significant spatial dependence, enhancing our understanding of the complex geospatial distribution of Au. These findings support the combined use of predictive modeling and spatial statistical methods to refine mineral exploration strategies, highlighting the value of advanced analytics in identifying promising exploration targets.

Effect of modified investment and casting system on the recasting properties of high-gold alloy

Background/purposeHigh gold (Au) alloys have many advantages, such as good mechanical properties and stable chemical properties for dental restoration. The purpose of this investigation was to investigate the effect of zirconia (ZrO2)-magnesia (MgO)-based investment combined with an argon arc vacuum pressure (Ar-arc VP) casting process on the recasting of high Au alloys. Materials and methodsThe recasting Au alloys were compared between the control group of conventional SiO2-based investment/horizontal centrifugal (HC) casting and the experimental group of ZrO2–MgO-based investment/Ar-arc VP die casting. The first-generation castings were defined as being made from purchased Au alloys and the second-generation castings were made from 50 wt% of the original Au alloys before casting, plus the balance of the remaining 50 wt% from the previous castings. The third-generation was made from all old surplus from the previous castings. The ingots were measured for the marginal gap, surface roughness, interface oxidation, hardness, and phase identification. ResultsThe results showed that the recasting success rate reached 100%. The ZrO2–MgO-based investment/Ar-arc VP group had better edge precision, smaller oxide layer thickness, and lower hardness than the SiO2-based investment/HC group. However, surface roughness analysis indicated little difference between the two groups. Phase analysis showed that the recasting alloys of the second and third-generation groups contained higher Au contents than those of the first-generation. ConclusionOverall, the Au alloy can be better recasted and retain good mechanical properties under the clinically used 5 wt% ZrO2–MgO-based investment/Ar-arc VP casting method.

Fluid source and ore-forming process of the Lishupo Au deposit, NE Hunan: Constraints from fluid inclusions, SIMS oxygen isotope, LA-ICP-MS pyrite trace elements and fsLA-ICP-MS quartz trace elements

The Lishupo Au deposit (4.3 t @ 4.76 g/t) is located in the central Jiangnan Orogen. The processes and origins of regional gold mineralization, as well as the characteristics of the ore-forming fluids, continue to be poorly understood. This study integrates field geology, fluid inclusions, secondary ion mass spectrometry (SIMS) O isotope, femtosecond laser ablation inductively coupled plasma mass spectrometry (fsLA-ICP-MS) trace elements analysis for quartz, and LA-ICP-MS for trace elements study of pyrite to constrain the nature and source of ore-forming fluids, mechanism of gold precipitation, and ore genesis. Field investigations and microscopic observations reveal three mineralization stages at Lishupo: (1) the quartz-pyrite (Qtz1-Py1) stage; (2) the quartz-dolomite-polymetallic sulfides-gold (Qtz2-Py2) stage; and (3) the quartz-carbonate-pyrite (Qtz3-Py3) stage.Cathodoluminescence (CL) observations reveal that Qtz1 and Qtz2 have a homogeneous texture, while Qtz3 exhibits oscillatory zoning. Fluid inclusions in quartz suggest a CO2-H2O-NaCl ± N2 ± CH4 fluid system, which comprise H2O-CO2-NaCl, CO2-rich, and aqueous types. Microthermometry of fluid inclusions indicates low salinity (stage 1: 3.7–7.9 wt% NaCl equiv.; stage 2: 2.2–7.5 wt% NaCl equiv.; stage 3: 1.4–3.9 wt% NaCl equiv.) and medium to low temperature (stage 1: 313–341 °C; stage 2: 209–286 °C; stage 3: 139–198 °C) for ore-forming fluids, consistent with the low Ti content (<10 ppm) found in the quartz. The low Al content (7.99–20.7 ppm) of Qtz1 suggests that the ore-forming fluids were saturated with CO2 and had a near-neutral pH. The Al contents are higher and more variable in Qtz2 (10.7–1959 ppm) and Qtz3 (21.6–713 ppm), which may imply fluctuations in fluid pH. δ18OFluid values for various types of quartz (Qtz1: 9.02–10.95 ‰, Qtz2: 6.30–7.68 ‰, Qtz3: 3.45–3.94 ‰) indicate a metamorphic fluid origin for stages 1 and 2 fluids, which were mixed with the meteoric water during stage 3. The highest concentrations of Au and As in Py2 suggest that the Qtz2-Py2 stage is the primary ore stage. The Co/Ni ratios of all types of pyrite are less than 1, indicating that the ore-forming materials are derived from metamorphic sedimentary rocks. Fluid inclusion microthermometry suggests that fluid immiscibility was responsible for the gold deposition during the Qtz2-Py2 stage. Fluid immiscibility destabilizes Au(HS)2-, leading to the precipitation of native gold. These data strongly suggest that the Lishupo gold deposit is classified as an orogenic-type deposit. Integrating the existing geochronology data and geological context, we emphasize the presence of the Late Triassic orogenic gold deposit in the Jiangnan orogen. This highlights a significant exploration target area within this zone for future gold prospecting.

SARS-CoV-2 nsp15 preferentially degrades AU-rich dsRNA via its dsRNA nickase activity.

It has been proposed that coronavirus nsp15 mediates evasion of host cell double-stranded (ds) RNA sensors via its uracil-specific endoribonuclease activity. However, how nsp15 processes viral dsRNA, commonly considered as a genome replication intermediate, remains elusive. Previous research has mainly focused on short single-stranded RNA as substrates, and whether nsp15 prefers single-stranded or double-stranded RNA for cleavage is controversial. In the present work, we prepared numerous RNA substrates, including both long substrates mimicking the viral genome and short defined RNA, to clarify the substrate preference and cleavage pattern of SARS-CoV-2 nsp15. We demonstrated that SARS-CoV-2 nsp15 preferentially cleaved pyrimidine nucleotides located in less thermodynamically stable areas in dsRNA, such as AU-rich areas and mismatch-containing areas, in a nicking manner. Because coronavirus genomes generally have a high AU content, our work supported the mechanism that coronaviruses evade the antiviral response mediated by host cell dsRNA sensors by using nsp15 dsRNA nickase to directly cleave dsRNA intermediates formed during genome replication and transcription.

Simultaneous Determination of Ultra-Trace Pt, Pd, Rh, and Ir in Gold Mining Residue by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) with an Antimony-Copper Fire Assay and Microwave Digestion

The evaluation of the flow direction of platinum group elements (PGEs) during gold-copper ore mining is challenging due to the uneven distribution and low content. Therefore, it is vital to accurately and simultaneously determine ultra-trace PGEs Pt, Pd, Rh, and Ir in gold mining residue samples. In this study, a method to simultaneously determine ultra-trace Pt, Pd, Rh, and Ir in gold mining residue is reported using Sb–Cu fire assay, microwave digestion, and inductively coupled plasma-mass spectrometry (ICP-MS). The Sb–Cu fire assay was used to enrich Pt, Pd, Rh, and Ir, obtaining Sb–Cu alloy particles that concentrate these elements. An optimal microwave method was employed to digest the Sb–Cu alloy particles. In ICP-MS, the collision reaction interface was used to eliminate the interferences of other elements and improve the accuracy. Moreover, the matrix-matched multi-external standards combined with internal standard calibration were utilized to reduce the error. High concentrations of Au, Ag, and Pb showed no interferences with Pt, Pd, Rh, or Ir determination. The limits of detection for Pt, Pd, Rh, and Ir were 0.018, 0.052, 0.064, 0.035 ng·g−1, respectively, and the relative standard deviation was 5.18, 4.66, 1.55, and 3.17%. Additionally, the determination of Pt, Pd, Rh, and Ir in standard reference materials showed good agreement with the certified values. In summary, a reliable and efficient method is provided to determine various PGEs which is of great significance for gold-copper ore mining.

Multistage evolution of gold mineralization in the Kibali gold district: Insights from pyrite analyses

The Kibali gold district, located on the Congo Craton, comprises a Neoarchean gold resource exceeding 28.7 Moz. The district is located within a westerly-verging stacked fold-and-thrust belt associated with a compressional tectonic regime active from ca. 2.64–2.60 Ga. Deposits are hosted by a major fault zone that consists of a complex series of smaller thrust faults, shear zones, and folds, which extend over 60 km. Gold deposits are primarily hosted in BIF and clastic sedimentary rocks. The gold and associated sulfides are in veins and disseminated in NE-to NNE-trending ore shoots within the deformed and metamorphosed volcanosedimentary rocks. Pyrite is the dominant sulfide mineral and hosts both solid solution gold and free gold. Because of its strong association with the gold mineralization, our study focusses on unravelling the metallogeny of the area by considering pyrite textural analyses, in situ trace element analyses using Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS), and S isotopic composition (δ34S) analyses using Secondary Ion Mass Spectrometry (SIMS).Eight distinct pyrite types were identified, including microcrystalline sooty (py-0a), small grains (<40 μm) (py-0b), aggregate recrystallized (py-1), core-rich inclusion (py-2), vein-like (py-3), non-zoned (py-4a), oscillatory As-bands zoned (py-4b), and cubic euhedral (py-5) pyrite. The ore-forming processes occurred over a polyphase evolution. Syn-diagenetic pyrite py-0a in volcaniclastic layers of older basin sediments served as the primary repository of Au (15.6 ppm median) with a near-zero δ34S value. Late diagenetic or early metamorphic pyrite (py-0b) was found in younger basin sediments. Py-1 resulted from solid-state recrystallization of py-0a and py-0b. During the early ore stage, porous py-2 with high Au concentrations (3.1 ppm) and various trace element enrichments precipitated due to fluid-rock interaction. Metal precipitation occurred through sulfidation and carbonation of wall rock with a relatively reduced fluid undergoing 34S-depletion. However, py-3 displayed notable trace element depletion and a complex mineral association. In a second ore stage, py-4a and zoned py-4b deposition occurred, dominated by an over-pressured fluid fracturing brittle rock. Py-4b, rich in Au (5.5 ppm) concentrated in oscillatory zoned As-rich bands, resulted from interactions during pulsed fluid flow. This process involved fluid phase separation, non-equilibrium conditions, 32S-depletion, and precipitation of py-4b with a high δ34S value (6.4 ‰ mean). Subsequently, pyrite (0–4) generations underwent deformation during a later ductile deformation event, leading to the remobilization and concentration of invisible gold into adjacent gold grains within the high-grade shoot plunging NE. This process involved shearing, boudinaging, and folding ore minerals in tightly folded structures. Late-stage py-5 formed under gold-poor fluid conditions or inefficient gold depositional conditions. Brittle fracturing of these grains later provided local sites for remobilized gold. The study contributes insights into the origin and evolution of gold mineralization in the Kibali gold district, supporting a multistage ore-forming fluid system.

Catalysis of Nickel-Based gold single-atom alloy for NO-CO reaction: Theoretical insight into role of gold atom in enhancing catalytic activity

Single-atom alloy (SAA) attracts great interest recently as excellent heterogeneous catalyst. Herein, the catalysis of Ni-based Au SAA for NO-CO reaction is investigated using DFT calculations. Under lean conditions, N2 formation occurs to produce NiOx surface, as observed experimentally, because CO2 formation cannot occur due to easy desorption of CO. Under rich conditions, CO2 formation occurs with small Ea value to afford (N)2-adsorbed surface. Next catalytic cycle starts with (N)2(NO)2-adsorbed surface because N2 formation needs larger Ea value but NO adsorption readily occurs with considerable energy stabilization. As Au-content increases, d-valence-band center lowers in energy to increase activation barrier for N–O bond cleavage of NO but decrease those of CO2 and N2 formations. Thus, rate-limiting step is N2 formation in low Au-content but N–O bond cleavage in high Au-content. A volcano-plot is presented against Au-content. The optimal Au-content is about 6 % on catalyst surface.

Supergene gold transformations of the placer gold deposits from the Gamba district in northern Cameroon: Implications for secondary and nano-particulate gold formations

The northern part of Cameroon is a Sudanese or Sudano-Sahelian type characterized mainly by a dry climate, a significant landscape position, and distance from the primary gold (Au) sources, giving the occasion to explore the study of complex supergene Au transformations. This study on the biogeochemical transformation of Au in Cameroon will expand understanding of this process and provide advantageous results for Au recovery from materials that are ultimately regarded as waste. In this study, placer Au particles were collected from four individual sites, Djaba, Bigbal, Bougma, and Mayo Salah, and analyzed using a scanning electron microscope (SEM), electron probe microanalysis (EPMA) and LA-ICP-MS Time of Flight (ToF) to observe nanometer-sized Au grain morphologies, the Au mobility and spatial association between Au and related major and minor elements by element distributions in Au particles, respectively. The results from the examination of Au samples across all sampling sites show that Au particles are formed by the binary Au/Ag alloys and that the formation of Au nano- and micro-particles is associated with Au/Ag dissolution and Au re-precipitation. The abundant nano- and micro-particles of Au morphotypes within the cavities of primary Au grains across all the sampling locations were associated with the polymorphic layers formed by clays, iron-oxides, and silicate minerals. The nano- and micro-particles of Au overgrow as colloids and crystalline phases of triangular, spherical, hexagonal, and octahedral platelet aggregates of bacteriomorphic Au and were indicative of biogeochemical transformation. The high Au concentrations in the rim suggest the dissolution of Ag and Cu involving Au mobility identified in placer Au grains across the individual sites. Hence, the minor elements, such as Ag and Cu, occur in solid solution in the Au cores, while trace elements, such as Si, Al, Fe, Cr, Ti, Ga, Ni, Pb, Mn, V, and As, form impurities or micro inclusions in the rim of native gold which was interpreted as evidence of Au mobility. Furthermore, the Au grains are commonly associated with pyrite, chalcopyrite, bornite, and galena. This can only be attributed to the hypogene orogenic precipitation environment, implying that Au grains were transported from primary sources. Overall, the Au particle transformation and mobility of placer Au highlighted in this study was a good indicator for understanding biogeochemical mechanisms affecting gold particles in the northern Cameroon supergene environments.

Insights Into Formation and Growth of Colloidal Multielement Alloy Nanoparticles in Solution through In Situ Liquid Cell TEM Study

AbstractThe nucleation and growth of nanoparticles are critical processes determining the size, shape, and properties of resulting nanoparticles. However, understanding the complex mechanisms guiding the formation and growth of colloidal multielement alloy nanoparticles remains incomplete due to the involvement of multiple elements with different properties. This study investigates in situ colloidal synthesis of multielement alloys using transmission electron microscopy (TEM) in a liquid cell. Two different pathways for nanoparticle formation in a solution containing Au, Pt, Ir, Cu, and Ni elements, resulting in two distinct sets of particles are observed. One set exhibits high Au and Cu content, ranging from 10 to 30 nm, while the other set is multi‐elemental, with Pt, Cu, Ir, and Ni, all less than 4 nm. The findings suggest that, besides element miscibility, metal ion characteristics, particularly reduction rates, and valence numbers, significantly impact particle composition during early formation stages. Density functional theory (DFT) simulations confirm differences in nanoparticle composition and surface properties collectively influence the unique growth behaviors in each nanoparticle set. This study illuminates mechanisms underlying the formation and growth of multielement nanoparticles by emphasizing factors responsible for chemical separation and effects of interplay between composition, surface energies, and element miscibility on final nanoparticles size and structure.

Pd-Ag-Au Minerals in Clinopyroxenites of the Kachkanar Ural–Alaskan-Type Complex (Middle Urals, Russia)

The study of noble metal minerals of the Ural–Alaskan-type (UA-type) complexes has been traditionally focused on their platinum-bearing dunites and chromitites, while clinopyroxenites have been poorly considered. In this study, we report the first detailed data on the noble metal mineral assemblage in clinopyroxenites of the Kachkanar intrusion, which is a part of a UA-type complex and is renowned for its huge Ti-magnetite deposits. High concentrations of Pd, Au and Ag are closely linked to Cu-sulfide mineralization in amphibole clinopyroxenites, in which they form Pd-Ag-Au minerals: keithconnite Pd3−xTe, sopcheite Ag4Pd3Te4, stutzite Ag5−xTe3, hessite Ag2Te, merenskyite PdTe, kotulskite Pd(Te,Bi), temagamite Pd3HgTe, atheneite (Pd,Hg)3As, potarite PdHg, electrum AuAg and Hg-bearing native silver. Among those, six mineral phases are first reported for clinopyroxenites of the Ural platinum belt. Our evidence supports a petrological model, suggesting that during fractionation of high-Ca primitive magmas at high oxygen fugacity, Pt, Os, Ir, Ru and Rh accumulate in early olivine–chromite cumulates, while Pd, Au and Ag reside in the melt until sulfide saturation occurs and then concentrate in sulfide mineralization. Subsequently, this sulfide mineralization is likely affected by cumulate degassing, which results in a partial resorption of the sulfides and Pd, Au and Ag remobilization by fluid. Second-stage concentration of the sulfides and the chalcophile noble metals in the amphibole-rich rocks may occur when H2O from the fluid reacts with pyroxenes to form amphiboles, and the fluid becomes oversaturated with sulfides and chalcophile elements.

Sulfur isotopic systematics of hydrothermal precipitates in the Okinawa Trough: Implication for the effect of sediments and magmatic volatiles

The Okinawa Trough is a sediment-covered intra-continental back-arc basin with active hydrothermal activities. The sulfur isotopic systematics of the hydrothermal systems in the Okinawa Trough remain unclear owing to the complex sulfur reservoirs. To address these uncertainties, we conducted in situ S isotopic combined with whole-rock geochemical, Pb isotopic, and barite Sr isotopic analyses of typical hydrothermal precipitates from three hydrothermal fields with varying sediments thickness (Iheya North Knoll (INK) < Yonaguni Knoll IV (YK) < Noho) in the Okinawa Trough. The δ34S values of barite from INK (+16.4‰ to +19.6‰, median + 18.5‰) and YK (+16.2‰ to +22.2‰, median + 19.5‰) mostly indicate lower values than those obtained for seawater (~ +21‰), combined with the observation of high S and O fugacity (fO2–fS2) mineral assemblages (e.g., low-Fe sphalerite ± enargite ± tennantite ± chalcopyrite), and high Cu and Au contents of hydrothermal precipitates, consistent with the addition of magmatic volatile to these two fields. In contrast, the in situ δ34S values of sulfide minerals from INK (+5.6‰ to +10.4‰, median + 9.0‰) and YK (+3.5‰ to +5.5‰, median + 4.7‰) fields were all positive, inconsistent with the S isotopic characteristics of H2S formed from SO2 disproportionation. We conclude that a large proportion of thermochemical SO42− reduction-derived heavy sulfur likely obscure the characteristics of H2S sourced from disproportionation. This was likely resulting from (1) sediment controlled long-scale lateral hydrothermal circulation, (2) the existence of early precipitated anhydrite, and (3) high concentrations of H2 in the high-temperature reaction zone. The Noho field have low δ34S values (−0.2‰ to +5.3‰, median + 0.9‰) of sulfide minerals, combined with high sediment contributions reflected by high Pb isotopic ratios and low-fS2–fO2 mineral assemblages (e.g., high-Fe sphalerite ± pyrrhotite ± isocubanite), which indicates that the low δ34S value sulfur was derived from leaching of biogenic pyrite in thick sedimentary strata by hydrothermal fluid. Near surface, the high-temperature discharging hydrothermal fluids interacted with different thicknesses of sedimentary strata and leached different proportions of biogenetic pyrite, resulting in a negative correlation of sedimentary strata thickness and sulfide δ34S values of the Okinawa Trough hydrothermal fields.

A modified paleoplacer model for the metaconglomerate-hosted gold deposits at Jacobina, Brazil

Evidence is presented that the metaconglomerate-hosted Jacobina gold deposits in Brazil represent paleoplacers that became partly remobilized during later metamorphic overprint analogous to Witwatersrand-type deposits elsewhere, notably in South Africa. This includes strong lithological and sedimentological control on the gold, presence of detrital minerals with gold inclusions, and detrital gold particles. Detrital, synsedimentary, and post-depositional pyrite types can be differentiated. Whereas the first two types can be linked to gold accumulation, the latter was associated with gold dispersion. Synsedimentary pyrite has the highest Au content, from which elevated Au concentrations in Archean rivers can be inferred. The nature and extent of post-depositional alteration, mainly in the course of the Paleoproterozoic Orogeny, distinguishes the Jacobina deposits from other Witwatersrand-type gold deposits. Phase equilibria and Zr-in-rutile thermometry indicate peak metamorphic temperatures of ca. 600 °C. Both Mg-chlorite and Fe-chlorite formed in disequilibrium at approximately 280–340 °C during retrograde metamorphism. An igneous signature in the chemistry of some of the tourmaline and the remobilization of gold associated with Fe-oxides, near intrusive rocks, point at a local magmatic influence on the post-depositional mineralization stage. Whether magmatic hydrothermal fluids added Au to the system at that stage remains to be determined. Remobilization during regional metamorphism was insufficient to form substantial ore bodies but led to purification of the initially detrital gold particles that now contain relatively little Ag and Cu and lack Hg.

Paleoproterozoic, Mesoproterozoic, and Paleozoic sedimentary successions of the Southwestern Amazonian craton: geochemistry, provenance, and post-sedimentary events

The Amazonian Craton is home to many Statherian to Calymmian taphrogenesis events that evolved over Large Igneous Provinces. The NW-SE faults on the Western Amazonian Igneous Belt (1.82–1.74Ga) and their reactivations, which facilitated the deposition of the Beneficente Group (1.76–1.60Ga), Prainha Formation (1.46Ga), and Alto Tapajós Group (Silurian-Devonian), are associated with these events in the southwest Amazonian Craton. Mineralogical composition, whole-rocks geochemistry, and Nd-Sr-Pb isotopic data show that the three sedimentary successions originated in the provinces of Rondônia-Juruena and Tapajós Parima, particularly during two rift stages. Beneficente Group deposition is associated with Paleoproterozoic Rift 1, while the Prainha Formation represents the post-rift 1, and Alto Tapajós Group deposition is associated with Paleozoic Rift 2. In addition, the Prainha Formation also received sediment supply from the Sunsás Province. These three sedimentary successions have an intrinsic relationship with the reworking of the local basement and their own reworking that occurred from the Paleoproterozoic to the Paleozoic. Autochthonous reworking, particularly in the Colíder and Beneficente groups, is demonstrated by Ti-magnetite grains, volcanic and arenite fragments in the Prainha Formation sublitharenite, and by angular microcline grains, high Au content, a Pb whole-rock isochron yielding the 1.796±0.096Ga age, and by vs 1/Rb relationship in Alto Tapajós Group. and flat REE patterns and some positive Eu anomalies in the Prainha Formation and Alto Tapajós Group record the influence of the mafic rocks of the Mata-Matá suite. A Pb-Pb whole-rock isochron allowed hydrothermal activity recognition at 1.32Ga in the Vila do Carmo Formation. This event was ratified by positive Eu/Eu* (1.3–1.43), Ce/Ce* (1.24–2.84), and Gd/Gd*(~1.5) anomalies. Finally, Nd model ages, geochemistry, and Sr isotopes allow for correlating the local basement and the overlaying sedimentary successions along the Columbia and Gondwana boundaries.

Middle Devonian Evandale porphyry Cu-Mo (Au) deposit, southwestern New Brunswick, Canada: Analysis of petrogenesis to potential as a source for distal intrusion-related epithermal gold mineralization

The 391.2 ± 3.2 Ma (U-Pb on zircon) Evandale Granodiorite of southwestern New Brunswick is quite a unique intrusive rock in the southern part of the northeastern Appalachians. This research examines the relationship between the porphyry Cu-Mo-(Au) and epithermal systems with Evandale Granodiorite and environs. This Middle Devonian multi-phase I-type granite intrudes along the northern boundary of the deformed Silurian sedimentary and mafic volcanic rocks of the Mascarene Basin. This granitoid is identified as an oxidized I-type system with adakitic geochemical signatures and associated porphyry Cu-Mo-(Au) mineralization, possibly linked to slab failure sourced from decompression melting of the lower crust caused by post-collisional uplift, similar to the Magaguadavic Granite to the southwest. The Evandale adakitic intrusion is divided into two phases that consist of (1) a calc-alkalic coarser phase ranging from medium- to coarse-grained, seriate to porphyritic granodiorite to monzogranite with metaluminous to peraluminous features, and (2) the later stage alkali-calcic fine-grained (to aplitic) locally porphyritic phase ranging from a monzogranite to syeno-granite with peraluminous characteristics. The primary mineralogy of the intrusive rocks consists of K-feldspar + albite + plagioclase + quartz + biotite + hornblende + apatite ± muscovite ± zircon, along with several alteration phases, such as biotite, chlorite, sericite, and calcite. Geochemical analyses (using INAA, ICP-MS, and XRF) indicate that both phases of the Evandale granodiorite show a high concentration of Cu (108 ppm) and Au (33 ppb) associated with the presence of pyrite, chalcopyrite, and arsenopyrite in the fine-grained dyke samples. Up to 6 ppm Mo was contained within the granitic phase, whereas lesser amounts of Mo were confined to the fine grained to aplite phases. Microprobe analyses of primary biotite as both phenocrysts and groundmass shows 0.55 avg. wt.% Cl and 0.21 avg. wt.% F, which are relatively concentrated compared to other high-grade porphyry deposits. Hydrothermally altered rocks, veins, and sulfides associated with the porphyritic suite result from buoyant magmatic-hydrothermal fluids from a deeper intrusion exsolving fluids (quenched porphyry related), depressurizing, and reacting with the host coarser grained granodiorite and even some of the dykes locally. Based on the geothermometry and geobarometry of amphibole (actinolite-magnesiohornblende), the crystallization temperature and pressure of the Evandale coarse-grained granite and aplite are 674–755 °C, 0.2–0.7 kbar (20–70 MPa) and 838 °C, 0.42–1.4 kbar (42–140 MPa), respectively. This is consistent with biotite formation at temperatures ranging from 670° to 760 °C, based on Ti-in-biotite thermometry. Also, zircon saturation temperatures of the earlier coarse-grained porphyritic granites and later fine-grained porphyry to aplitic dykes are 736 °C and 787 °C, respectively. Spatially and temporally associated gold deposits beside Evandale and within this region of southwestern New Brunswick suggests that these oxidized I-type intrusions are a potential source for distal, low sulfidation epithermal gold deposits in the region.

Noble and base metal geochemistry of late- to post-orogenic mafic dykes from central Spain

The post-tectonic and post-orogenic mafic rocks from the Spanish Central System (SCS) (Iberian Massif) include dyke swarms of shoshonitic (microgabbros) and alkaline (lamprophyres and diabases) geochemical affinity, which register the nature of the metasomatic lithospheric mantle under central Spain. Such magmas sometimes show a direct (or indirect) relationship with the formation of orogenic and intrusion-related gold deposits, which are relatively abundant in the Iberian Massif. The noble and base metal composition of these intrusions shows Primitive Mantle-normalized patterns characterized by positive Au and Co anomalies and fractionated platinum group elements (PGE): from lower Ir-group PGE (IPGE; Ir–Ru) to higher Pd-group PGE (PPGE; Rh–Pt–Pd). The low contents of PGE, together with the base metal contents of pyrite (which is the dominant sulphide phase in the alkaline dykes), is in accordance with low degrees of mantle partial melting and the early segregation of sulphides during magma differentiation. The scarcity of PGE mineral deposits in the Iberian Massif could be explained in part by the apparent lack of PGE enrichment in the Iberian lithospheric mantle. On the contrary, the positive Au anomaly of the SCS mafic dykes represents relatively high Au contents, similar to (and higher than) those of mafic rocks derived from metasomatized subcontinental lithospheric mantle underlying Au-endowed cratons. Several geochemical features point to subduction-related metasomatism of either oceanic or continental nature as the main source of Au enrichment. The Au re-fertilization of the lithospheric mantle under central Spain makes it a potential source in the formation of gold mineralizations.

In Situ Trace Element and Sulfur Isotope Composition of Pyrite from the Beiwagou Pb-Zn Deposit, Liaodong Peninsula, Northeast China: Implications for Ore Genesis

The Beiwagou Pb-Zn deposit, located in the western part of the Liaodong Peninsula, is a carbonate-hosted stratiform deposit with a Pb + Zn reserve of 0.08 Mt @ 4.14% (Pb + Zn). The orebodies occur as conformable layers and lenses and are strictly controlled by strata (the Paleoproterozoic Gaojiayu and Dashiqiao Formations) and lithology (plagioclase amphibolite and dolomitic marble). Given that previous studies have focused only on the mineralization features and mineralogy of deposits, herein, we report in situ trace element analyses of pyrite using LA-ICP-MS, together with in situ sulfur isotopes of pyrite, to constrain the composition, substitution mechanisms, source of sulfur, and sulfate reduction pathways of pyrite in the Beiwagou deposit. Based on pyrite morphology, texture, and chemistry, four pyrite types were identified: subhedral, porous-to-massive pyrite (Py1) related to chalcopyrite; subhedral, porous crushed pyrite (Py2) associated with fine-grained sphalerite; rounded and porous pyrite (Py3) related to the Zn-rich part of the laminated ore; and anhedral, porous-to-massive pyrite (Py4) associated with pyrrhotite, arsenopyrite, sphalerite, and galena. Py1 is characterized by high As, Ag, Cd, In, Au, Cu, and Zn concentrations and low Te, Bi, and Mo concentrations, whereas Py2 has high concentrations of Co and Ni and low concentrations of other trace elements, such as Cu, Zn, Bi, and Te. Py3 is characterized by elevated As concentrations, low Co, Ni, In, W, Te, and Tl concentrations, and varying Pb concentrations, whereas Py4 has low Ag, Cd, In, Zn, Cu, and Mn concentrations and varying W, Co, Ni, Pb, Sb, and As concentrations. Significant correlations between some elements in each pyrite type suggest substitution mechanisms, such as (Zn2+ + Cu2+ + Mn2+ + Cd2+) ↔ 2Fe2+, Ag+ + (Sb)3+ ↔ 2Fe2+, and (Te+ + Ag+) + Sb3+ ↔ 2Fe2+, and the existence of a negative correlation between Co and Ni implies competition between both elements. The strongly positive δ34S values (12.11‰–23.54‰) are similar to that of seawater sulfates and likely result from thermochemical sulfate reduction (TSR). In conclusion, the Beiwagou Pb-Zn deposit is a typical SEDEX deposit and mineralization likely occurred during diagenesis.

Wafer-Level Au—Sn Solid-Liquid Interdiffusion Bonding for Microwave Applications

Future compact integration of microwave modules will require intermetallic bonding with pitch connections lower than 10 μm. Solid-liquid interdiffusion (SLID) bonding is a potential bonding method for close heterogeneous integration because of its bonding temperature in the range of solder bonding, its ability to withstand higher temperaturs than bonding and its moderate compatibility with the joining of rough surfaces. This paper presents the results of an investigation of the Au—Sn system for integration of A3B5 chips on wafer level using SLID bonding. A sequence of five layers of Au and Sn with weight ratios of about 3:2 was deposited on a sapphire substrate. The structure and phases of the obtained system were investigated before and after annealing. The initial system has five distinctive alternating layers with an overall thickness of around 4.5 μm. After heat treatment at 320 °C with a holding time of 10 minutes, the Au—Sn system transforms into one layer that consists of only one phase ζ (Au0.853Sn0.147). The homogenization process is completed in less than 10 minutes. The ζ phase, of which the system is composed after annealing, has a melting point of 522 °C, which ensures the high temperature stability of the bonding layer. Bonding using the formed system was conducted. Morphology, elemental composition, and the initial mechanical properties of bonded structures have been studied. There are two types of defects in the joint's cross section: voids and the presence of local interfaces between two surfaces (an unbonded-like line). EDX analysis of the cross section of the joint between two crystals shows that the average ratio of Sn to Au over the cross section of the joint is 10.7 %. The complex of studies conducted suggests that the bonding area mostly includes the ζ phase, which will provide the best mechanical strength characteristics among the phases with a high Au concentration. The average bond shear strength is 32 MPa. Initial robustness results of the bonding are promising for space applications.