Au Deposits Research Articles

Optimization of the synergistic effects in polycrystalline Pt–Au electrodes in developing an effective arsenic sensor via oxidation reactions

An Au-modified Pt electrode, prepared via 8 cycles of Au deposition using cyclic voltammetry, shows enhanced As(iii) oxidation. The Au(111) and Pt(111) facets, with favorable As(iii) adsorption, coupled with Pt–Au synergy, facilitate the oxidation.

Homochiral Nanopropeller via Chiral Active Surface Growth.

Under the control of chiral ligand glutathione and in the presence of hexadecyltrimethylammonium bromide, Au deposition on Au seeds is known to give chiral nanostructures. We have previously shown that the protruding chiral patterns, as opposed to flat facets, are likely caused by active surface growth, where nonuniform ligand coverage could be responsible for the focused growth at a few active sites. By pushing the limit of such a growth mode, here, we use decahedral seeds to prepare homochiral nanopropellers with intricate patterns of deep valleys and protruding ridges. Control experiments show that the focused growth depends on the rates of Au deposition by changing either the seed concentration or the reductant concentration, consistent with the proposed mechanism. The dynamic growth competition between the ligand-deficient active sites and the ligand-rich surfaces gradually focuses the growth onto a few active sites, causing the expansion of grooves, squeezing of steep ridges, and a surprising 36° rotation of the pentagonal outline. The imbalanced deposition on the prochiral slopes is responsible for the tilted grooves, the twisted walls, and thus the well-separated and distorted blades, which become the origin of the chiroptical responses.

Genesis of tungsten mineralization in the Yangla copper-polymetallic deposit, northwest Yunnan, China: Evidence from in situ U-Pb dating, trace elements, Sr isotopes, fluid inclusions, and H-O isotopes of scheelite

Scheelite is one of the main ore minerals in tungsten deposits, and its geochemical features can be used to examine and constrain tungsten mineralization. The Yangla deposit is one of the most important Cu-polymetallic skarn-porphyry deposits in the “Sanjiang” polymetallic metallogenic domain, Southwest China, hosting 150 Mt of Cu ores with economic concentrations of Pb, Zn, and Sb. The newly discovered tungsten mineralization in the Yangla deposit remains poorly understood. Hence, in order to ascertain the timing of tungsten mineralization, investigate its genetic relationship with magmatism and ore genesis, and elucidate the source, nature, and evolution of the ore-forming fluids, we performed a combined study of geochronology, in-situ trace elements, fluid inclusions, H-O isotopes, and in-situ Sr isotopic compositions of scheelite. In-situ U-Pb dating of scheelite showed that the timing of tungsten mineralization was 30 Ma. This mineralization age is significantly later than the published Cu mineralization age (∼230 Ma), skarn (∼231 Ma), and granitoid emplacement age (∼230 Ma) in the Yangla ore district. In-situ trace element analyses revealed that scheelite is depleted in Mo, Mn, and Ta and slight enriched in Sr, Y, REEs, and Au. It is also characterized by HREE-depleted chondrite-normalized patterns with strongly positive Eu anomalies. Our data reveal that 3Ca2+ = (2REE)3++□Ca (site vacancy) is the main substitution mechanism that controls REEs in scheelite. The low concentrations of Mo, negative Ce anomalies, and positive Eu anomalies of scheelite indicate a reduced condition. Preliminary REEs features indicate that the genesis of scheelite may be related to vein-type W (Au) deposits. The homogenization temperatures for fluid inclusions present a strongly decreasing trend (328 to 173 ℃), indicate that cooling is the predominant mechanism for the formation of scheelite. The δD and δ18Ofluid values from fluid inclusions of scheelite vary broadly from −161.70 ‰ to −133.30 ‰ and from 6.32 ‰ to 9.80 ‰, respectively, indicating a mixture of magmatic and meteoric water, with possible involvement of magma degassing and fluid–rock interaction. The initial 87Sr/86Sr ratios of scheelites (0.71931– 0.72117) are significantly higher than those of the granodiorite (0.71149 – 0.71990) and basalt (0.70562 – 0.70995) in the Yangla ore district, indicating that the Oligocene magmatism and Devonian marble with radiogenic Sr isotopic compositions contributed to tungsten mineralization. The fluid-rock interaction between the ore-forming fluids derived from the concealed granitoids and the Devonian wall rocks may play an important role in tungsten mineralization and provide significant Ca for scheelite precipitation. Thus, the tungsten mineralization should be associated with Oligocene magmatism, ruling out the genetic relationship with Late Triassic magmatism and being significantly different from the skarn-porphyry Cu-Pb-Zn mineralization at Yangla.

Re–Os isotopes and geochemistry of pyrite from the Dongguashan Cu(-Au) deposit, Eastern China: Implications for porphyry-skarn-stratabound mineralization systems

Stratabound deposits are widely distributed along the Middle-Lower Yangtze River metallogenic belt (Eastern China). The stratabound mineralization system in these stratabound deposits remains enigmatic as to whether it is associated with late Mesozoic intrusions or late Carboniferous sedimentary exhalative processes. Dongguashan is a typical stratabound deposit and is characterized by pyrite that formed in porphyry-skarn-stratabound orebodies, which makes it ideal for comparing porphyry, skarn, and stratabound mineralization systems by pyrite study. We classify pyrite types according to occurrence and generation. Specifically, the pyrite in the porphyry orebodies is composed of Py-p1 (potassic zone) and Py-p2 (propylitic and phyllic zone). Py-s, among garnet grains, occurs in the skarn orebodies. From top to bottom, the pyrite in the stratabound orebodies is composed of macrocrystalline pyrite (Py-m) in the massive mineralization zone, Py-l in the laminated mineralization zone, and coarse-grained pyrite (Py-v1) and microcrystalline pyrite (Py-v2) in the vein-like mineralization zone. Co, Ni, Se, As, and Au are most likely to occur as solid solutions in the Dongguashan pyrite. Pb and Bi are likely distributed in Dongguashan pyrite homogeneously as nanoinclusions. The Zn, Cu, and Mo in Dongguashan pyrite indicate that these elements occur as micromineral inclusions. The positive correlation between S and Fe, high Co/Ni ratios (mostly > 2), and coexistence with hydrothermal minerals imply a magmatic-hydrothermal origin for the Dongguashan pyrite. Py-m yields a Re–Os isochron age of 135.8 ± 2.8 Ma (MSWD = 1.8), which is interpreted as the stratabound ore-forming age. Combined with previous results, the porphyry-skarn-stratabound mineralization is the product of the same hydrothermal fluid system related to Early Cretaceous magmatic activity.

Silver isotope analysis and systematics of native gold from the Rajapalot Co-enriched gold deposit, Finnish Lapland

Silver is probably the closest isotopic proxy to track monoisotopic gold and has been shown to have great potential to yield new information on the origin and enrichment processes of gold. This study describes the development of a tailored analytical protocol for accurate analysis of Ag isotopes and provides the first Ag isotope data for the Paleoproterozoic Rajapalot Au-Co deposit, Finnish Lapland. Six native Au samples yield ε109Ag values (relative to NIST SRM 978a) from −6.8 to +2.1 and are within the range of Ag isotopic compositions reported for native Au samples. The mean of the analyzed Au samples is ε109Ag = −3.8 ± 1.7 (2SD) with most of the samples with negative ε109Ag values (−6.7 to −2.0); one sample has a positive ε109Ag value of +2.1 ± 0.5. Silver isotope fractionation in the Rajapalot Au deposit was likely associated with physicochemical processes related to deposition and/or re-mobilization of the ore rather than with source region inheritance. It is suggested that redox reactions involving Ag+ ↔ Ag0 phase change primarily account for the isotopic differences within the deposit. Our results also suggest that the Rajapalot Au-Co deposit was formed via multistage ore-forming processes and/or that the primary ore was re-mobilized, which caused isotope fractionation along fluid pathways. Silver isotope variation within a deposit may mark a fractional crystallization trend with the lightest isotopic composition representing the earliest precipitate. Hence, Ag isotopes show potential as an isotopic vectoring tool in search of Au-enriched domains.

Permian−Triassic magmatism above a slab window in the Eastern Tianshan: Implications for the evolution of the southern Altaids

Permian−Triassic metaluminous−peraluminous granitoids, mafic−ultramafic plutons, and Ni-Cu and Au deposits are prominent features in the Eastern Tianshan of the southern Altaids. However, the genetic relationship between coeval granitoids and mafic−ultramafic intrusions, and the geodynamics of magmatism and related mineralization, remain ambiguous. To address these ambiguities, we present petrological, geochemical, and bulk-rock Sr-Nd-Fe and zircon U-Pb-Hf isotope analyses of granitoids from the Shuangchagou Complex and gabbros from the Huangshandong Complex in the Eastern Tianshan. Zircon U-Pb ages demonstrate that the Huangshandong gabbro was emplaced at ca. 277.8 ± 1.4 Ma. In contrast, U-Pb ages determined from zircons in the granitic rocks of the Shuangchagou Complex suggest that the complex crystallized from three stages of magmatism: (1) strongly peraluminous S-type granitic magma represented by early-stage gneiss and granitic veins (ca. 289 Ma), (2) metaluminous to weakly peraluminous I-type granitic magmas represented by the intermediate-stage granitoids (ca. 283−261 Ma), and (3) late-stage granitoids (ca. 250−241 Ma). The intermediate- and late-stage granitoids (ca. 283−241 Ma) show clear enrichments in the light rare earth elements and large ion lithophile elements (e.g., Rb, Th, and U), and depletions in high field strength elements (e.g., Nb, Ta, and Ti), similar to arc magmas, which indicates that the North Tianshan oceanic plate was still subducting during the Middle Triassic. Considering the diversity of magmatic rocks (e.g., mid-oceanic-ridge−type mafic rocks, and I-, S- and A-type igneous rocks), mineralization styles (e.g., Alaskan-type Ni-Cu sulfide deposits and orogenic gold deposits), and the dextral strike-slip faults (e.g., Kanggur Fault) that occurred concurrently in the Eastern Tianshan during the Early Permian to Middle Triassic, we suggest that splitting of the subducted portion of the North Tianshan oceanic plate created a slab window that allowed the upwelling and partial melting of asthenospheric mantle to form the mafic−ultramafic intrusions and related Ni-Cu sulfide deposits. Sustained migration of magma provided the heat necessary to induce partial melting, devolatilization, and desulfurization of crustal materials, producing the Permian−Triassic, high-K to calc-alkaline I- and S-type granitoids, and associated orogenic gold deposits. By integrating the results of this study with published work regarding the Kanggur Accretionary Complex, we suggest that the subduction of the North Tianshan Ocean may have lasted until the Late Triassic.

Enhancement of Metal Nanostructure Deposition on Silicon Laser-Induced Periodic Surface Structures by Galvanic Replacement.

We report a chemically motivated, single-step method to enhance metal deposition onto silicon laser-induced periodic surface structures (LIPSSs) using reactive laser ablation in liquid (RLAL). Galvanic replacement (GR) reactions were used in conjunction with RLAL (GR-RLAL) to promote the deposition of Au and Cu nanostructures onto a Si LIPSS. To increase the deposition of Au, sacrificial metals Cu, Fe, and Zn were used; Fe and Zn also enhanced the deposition of Cu. We show that the deposited metal content, surface morphology, and metal crystallite size can be tuned based on the difference in electrochemical potentials of the deposited and sacrificial metal. Compared to the Au and Cu reference samples, GR more than doubled the metal content on the LIPSS and reduced metal crystallite sizes by up to 20%. The ability to tune the metal content and crystalline domain size simultaneously makes GR-RLAL a potentially useful approach in the manufacturing of functional metal-LIPSS materials such as surface-enhanced Raman spectroscopy substrates.

Petrogenetic of Igneous Complex of Ilota Nanasi Gold Deposit, Gunung Pani, Gorontalo, Indonesia

Ilota Nanasi Au-Ag deposit located in the western flank of the Gn. Baganite, a part rhyodacite dome in Gn. Pani district, Gorontalo Province, where the extensive exploration programs were carried out by PT Gorontalo Sejahtera Mining (a subsidiary of PT J Resources Nusantara) from 2012 – 2020. As the result, a total of 72.7 Mt @ 0.98 g/t Au and 0.85 g/t Ag (2.3 Moz Au and 2.6 Moz Ag) mineral resource was delineated in 2019. This paper mainly aimed to the petrogenesis association of granitoid basement and rhyodacite unit as the host rock in the Ilota Nanasi gold deposit. The geology of Ilota Nanasi is overlain by Late Miocene granodiorite, andesite and diorite basement, Pliocene volcanic complex predominantly dacite – rhyodacite, tuff, breccia, and quaternary deposit as alluvial and surface breccia. Hydrothermal alteration and gold – silver mineralization centered in the porphyritic rhyodacite host rocks where the intense silicification forming a zone around the hydrothermal crackle breccia unit and/or high-density quartz vein, veinlets and stockworks. Mineralization in Ilota Nanasi is interpreted as a low sulfidation epithermal system dominated by a large volume of hydrothermal crackle breccia, intense quartz veining, veinlets, and high-density fracturing. A combined analytical result of petrography and whole-rock geochemistry has been used to assess the petrogenetic association of the rhyodacite and granitoid basement in the Ilota Nanasi. The result of the AFM diagram plot shows sample trends in calc-alkaline magma field. In contrast, the SiO2 – K2O plot distributed in two trends: the older unit was associated with high-K calc-alkaline and the shoshonite series for the younger unit. The changing of magma series is considered as product of crystallization differentiation of evolved parental magma or derived from the melting of mantle material after the mantle or lower crustal was metasomatized during a former episode of subduction.

Geogas-Carried Metal Prospecting for Concealed Ore Deposits: A Review of Case Studies in China

Geogas-carried metal prospecting, an integral part of deep-penetrating geochemistry, is potentially effective in the geochemical exploration of concealed ore deposits. However, its principles and applicability remain controversial. This study summarizes and discusses the progress in geogas-carried metal prospecting in China. The method comprises three constituents: geogas, nanoparticles, and their vertical transportation. Researchers have failed to determine the exact contributions of different sources of geogas. Studies on Pb isotopes, rare earth element patterns of geogas, the comparisons between metals in soil, geogas, and ore geochemistry, and characteristics of nanoscale metals in earthgas (NAMEG), confirmed the relationship between NAMEG and concealed ore deposits. A statistical analysis of field experiments and applications showed that geogas-carried metal prospecting is applicable for the geochemical exploration of magmatic and hydrothermal Cu, Au, Zn, Pb, U, Sn, and Ag deposits and is suitable for most geochemical landscapes except deserts and cold swamps. Finally, genetic models of NAMEG anomalies were constructed. High-permeability migration channels are critical in the formation of NAMEG anomalies over concealed ore deposits. Future work entails applying geogas-carried metal prospecting to certain types of ore deposits and geochemical landscapes and studying NAMEG to provide quantitative information for targeting concealed ore deposits.

The lithospheric cycle of ore-forming ingredients and the resultant recurrent ‘flare-ups’ of porphyry Cu deposits: Examples from the Yidun Arc, eastern Tibet

The porphyry Cu deposits with distinct mineralisation ages frequently occur as recurrent ‘flare-ups’ in a narrow region; however, the reasons controlling their occurrence are still debated. The eastern Yidun Arc in eastern Tibet produced a cluster of porphyry Cu deposits of the late Triassic and late Cretaceous ages, making it the ideal location for conducting this research. As a result, we use the late Triassic Xuejiping Cu–(Au) and late Cretaceous Hongshan–Hongniu Cu–Mo deposits as research objects, compiling new and published geochronological, elemental, and Sr–Nd–Hf isotopic data from their ore-forming porphyries to shed light on the above issue. The zircon U–Pb ages of the Xuejiping and Hongshan–Hongniu porphyries are 217.8 – 217.9 Ma and 78.7 Ma, respectively, and display adakitic characteristics. The Xuejiping porphyries present enriched Sr–Nd–Hf isotopes (0.70529 – 0.70590, −3.30 – −1.09, 0.40 – 2.20, respectively), low (Gd/Yb)N (2.24 – 3.20) and Nb/Ta (12.8 – 15.9) ratios, relatively high Nb (14.9 – 20.0 ppm) and Zr/Sm (23.4 – 41.5) values, indicating their origin in the partial melting of enriched mantle that is metasomatised by slab-melts and fluids in subduction zone. Furthermore, the Hongshan–Hongniu porphyry is adakitic, like the late Triassic igneous rocks in this area. Its Sr–Nd–Hf isotopes (0.69873 – 0.70996, −10.7 – −6.72, −14.9 – −0.50, respectively) are close to the isotopic evolution line of the late Triassic Xuejiping intrusions and show a trend towards the regional crystalline basement, which signify that the Hongshan–Hongniu porphyry mainly originated from the late Triassic juvenile crust, with some contributions from crystalline basement. One highly fractionated sample (i.e. HZK17-11-76) has extremely evolved Sr–Nd isotopes (0.70996 and −10.7, respectively), indicative of assimilation of sedimentary rocks. The new genetic models of the late Triassic and late Cretaceous porphyries in the Geza Arc show that the westward subduction of the Garzê–Litang oceanic crust in the late Triassic triggered the occurrence of the highly oxidised and Cu–S–H2O rich adakitic melts in the middle–lower crust, which evolved to amphibole cumulates and porphyry Cu–(Au) deposits (i.e. Xuejiping) in the upper crust. In the late Cretaceous, the extensional environment triggered the re-melting of late Triassic juvenile cumulates and Mo-rich crystalline basement, resulting in Cu–Mo–S–H2O-rich, highly oxidised magma. Through fractional crystallisation and assimilation of Mo-rich sedimentary rocks, the magma eventually transformed into Hongshan–Hongniu porphyry-(skarn) type Cu–Mo deposits. In summary, we conclude that the periodic recycling of the ore-forming ingredients on a lithospheric scale from slab subduction to post-subduction periods controls the recurrent ‘flare-ups’ of PCDs in this confined area.

Geochemistry and geochronology of Beiya giant Au polymetallic deposit: Implications for multistage ore-fluid pulses in a skarn system

Garnet is one of the most typical minerals in skarn deposits, and its texture and composition is a proxy for the changing physicochemical conditions. Thus, mineralogical and geochemical characterization of different garnet types can provide important information on the nature and evolution of ore-forming fluids. The Beiya gold-polymetallic deposit is China’s largest skarn-type Au deposit with Au reserves of >380 t. Although several studies have addressed the skarn formation mechanism and nature of fluid evolution, a systematic study on the changes in the composition and texture of garnet from wall rocks to ore-related intrusion has not yet been attempted. In this work, we carry out a systematic investigation along a horizonal profile in the open pit of the Beiya deposit. Our results show that the garnet in the profile belongs to grossular-andradite solid solution series with all grains showing well-developed fine oscillatory zoning. The garnets are of two types: the first type (Grt I) formed within the endoskarn, is reddish to red with euhedral-subhedral megacryst structure (>10 mm) and has altered surfaces. The second type (Grt II) occur in the proximal exoskarn, is red to brown–red, euhedral-subhedral, with medium- to fine- grained structure (0.3–4 mm) and displaying oscillatory zoning. Unlike Grt I, hydrous minerals occur in the pores among Grt II garnets, such as calcite, quartz, epidote and chlorite. Also, calcite-chlorite vein, quartz vein and quartz-chalcopyrite-pyrite vein cuts the Grt II garnets. Grt I is dominantly grossular (Adr14.88-43.58Grs55.25-82.87), depleted in the large ion lithophile elements (LILE), relatively enriched in high field strength elements (HFSEs) and enriched in heavy rare earth elements (HREEs) with negative Eu anomalies. Grt II is mostly andradite (Adr62.18-98.91Grs0-36.22), depleted in the LILE and HFSE, enriched in light rare earth elements (LREEs) with slightly positive Eu anomalies. Here we selected Grt II for in-situ LA-ICP-MS U-Pb dating, since Grt I contains negligible uranium. The results yielded a lower intercept 206Pb/238U age of 35.3 ± 1.8 Ma (MSWD = 0.68, n = 23). The calculated oxygen isotopic compositions of hydrothermal fluids in equilibrium with two types of garnets range from 6.46 ‰ to 8.56 ‰ (average 7.89 ‰), which are within the range of values for magmatic fluids. We infer that the physicochemical conditions of the hydrothermal fluid changed from relatively reduced, nearly neutral, and low water/rock ratios to slightly oxidized, slightly acidic, and high water/rock ratios. The chlorine content in the fluid increased during garnet growth. The fluctuating compositions of garnets in the skarn suggest multistage ore-fluid activities and the fluid evolution provide insights into the ore-forming process.

Late Mesozoic tectonic evolution and thermal history in the northeast Xing'an Block, NE China: Implications for gold mineralization and preservation

Late Triassic–Jurassic orogenic and Early Cretaceous epithermal Au deposits are significant producers of Au, Ag, and potentially critical elements (e.g., Te, Se and Sb) in the North Heilongjiang Belt in the Xing'an Block, NE China. However, the preservation mechanism of these Au deposits associated with tectonic evolution is unclear. Here, we conducted zircon U–Pb, sericite Ar–Ar, zircon and apatite (U–Th)/He dating as well as whole‐rock geochemistry in the Xing'an Block. Zircon U–Pb dating shows the ages of 174.1 ± 2.4 Ma for the granodiorite, 169.9 ± 1.6 Ma for the tonalite, 154.0 ± 2.0 Ma for the monzogranite and ca.122 Ma for the diorite. Sericite Ar–Ar dating presents plateau and isochron ages of 163.2 ± 1.8 Ma and 163.4 ± 2.8 Ma. The average apatite (U–Th)/He (AHe) and zircon (U–Th)/He (ZHe) ages from the Jurassic rocks have the ranges of ca. 146–89 Ma and ca. 150–116 Ma and from the Cretaceous are ca. 109–76 Ma and ca. 117–111 Ma, respectively. The Early‐Middle Jurassic intrusions are featured by the tonalite‐trondhjemite‐granodiorite (TTG) rock type. Late Jurassic monzogranite has the geochemical signature of adakitic rocks. The Early Cretaceous granitoids are classified as volcanic arc granites with a part of the Early Cretaceous granodiorite featured by adakitic. These new results reveal five group ages associated with tectonic evolution, Au mineralization and the preservation of the Au deposits. (i) Magmatic events were related to the subduction of the Mongolia‐Okhotsk Ocean during the Early Jurassic (ca. 177–170 Ma) and then the compressional settings with regional deformation (ca. 167–163 Ma). (ii) Thickening crust and orogenic Au mineralization were related to the closure of the Mongolia‐Okhotsk Ocean (ca. 154–145 Ma). (iii) The transformation was from compressional to extensional settings followed by exhumation during the Early Cretaceous (ca. 145–120 Ma), which is the factor of the exhumation of the orogenic Au deposits formed from the Late Triassic to Late Jurassic. (iv) Epithermal Au–Ag mineralization was associated with an extension related to the subduction of the Palaeo‐Pacific Plate (ca. 120–100 Ma). (v) Thermal history shows one thermal event during the Late Cretaceous (ca. 89–76 Ma). The Au deposits have been preserved since the Late Cretaceous.

Precious-Metal Mineralization and Formation Conditions of the Biche-Kadyr-Oos Epithermal Au-Ag Ore Occurrence (Eastern Sayan, Russia)

The Biche-Kadyr-Oos epithermal Au-Ag ore occurrence is a prospective object in the Ak-Sug porphyry copper ore cluster (Eastern Sayan) in the northern part of the Central Asian orogenic belt (CAOB). The mineralization consists of gold-sulfide-quartz and gold-polysulfide-carbonate-quartz veins with argillic zones in the Lower Cambrian volcanic-sedimentary rocks. The origin of the Au-Ag ore occurrence is still debatable. To determine the origin, we examined the mineralogical and geochemical features, conditions of formation, and fluid sources of the Biche-Kadyr-Oos ore. A mineralogical and geochemical investigation outlines three stages of mineral formation: early argillic stage; gold-sulfide-quartz stage with pyrite, marcasite, pyrrhotite, arsenopyrite, chalcopyrite, less frequently sphalerite, hessite, gold, and electrum; and late gold-polysulfide-carbonate-quartz stage with gold, electrum, Hg-electrum, Se-acanthite, Se-galena, bornite, tennantite, tetrahedrite, hessite, tellurobismuthite, bismuthinite, matildite, jamesonite, ourayite, native Bi, and barite. Fluid inclusion study (thermometry, Raman spectroscopy) in quartz and mineral thermometry (electrum and sphalerite paragenesis) determined that ore veins were formed at P~0.5 kbar from CO2-water Na-K-chloride fluid (4.9–9.6 wt % NaCl eqv) and temperatures from 300 to 200 °C (early gold-sulfide-quartz veins at 300–230 °C, and late gold-polysulfide-carbonate-quartz veins at 290–200 °C) and variations in fO2, fS2, fSe2 and fTe2. The S isotopic composition in sulfides and δ34SH2S values of the fluid are +1.3‰ and +4.7‰, respectively, (T = 300–275 °C) indicating magmatic S in ore formation. The oxygen isotope data indicate that during the formation of veins, the magmatic fluid mixed with meteoric water (δ18Ofluid is from +3.4 to +6.4‰). The isotopic data that were obtained combined with mineralogical and geochemical features and conditions of ore formation indicate the similarity of Biche-Kadyr-Oos ore occurrence with epithermal Au-Ag deposits of intermediate sulfidation (IS) type. The presence of epithermal Au-Ag mineralization of the Biche-Kadyr-Oos IS type in ore cluster of the Ak-Sug Cu-Au-Mo porphyry deposit indicates the existence of a single porphyry-epithermal ore-magmatic system.

Cadmium sulfides: Electrochemical CO2 reduction and Fischer–Tropsch synthesis pathways

The development of electrocatalysts is a pivotal aspect of advancing electrochemical (EC) CO2 recycling. In this research, we incorporated cadmium sulfide (CdS) onto a cadmium (Cd) support and subsequently enhanced it with the deposition of Au, Ag, and Cu using sputter deposition techniques. These modified catalysts were then rigorously evaluated for their performance in EC CO2 reduction. The primary products were formate, CO, and H2. Notably, CdS/Cd demonstrated significantly superior performance in EC CO2 reduction compared to the unmodified Cd catalyst. Furthermore, the deposition of transition metals drastically suppressed H2 production, while Ag and Cu deposition enhanced CO production in NaHCO3 conditions. For Au/CdS/Cd in phosphate condition, CH4 and alkane-dominant C2–7 hydrocarbons were significantly produced and explained by the conventional Fischer–Tropsch synthesis paths. After EC CO2 reduction, CdS/Cd surface was observed to be recrystallized to CdCO3 with a morphology of cubes. Photocatalytic CO2 reduction over CdS/Cd produced CO, CH4, CH3OH, and alkene-dominant C2–6 hydrocarbons. Additionally, a zinc sulfide (ZnS) on Zn electrode was prepared and tested, which showed H2 and CO as main products, but no formate was observed.

Deep epithermal Au mineralization at Tuanjiegou, northeast China

To better understand the physicochemical features of deeply mineralized intervals of low-sulfidation (LS) Au deposits, the Early Cretaceous Tuanjiegou Au deposit in northeastern China was characterized as it comprises alteration and mineralization styles that reflect deeper portions of the mineralizing system. From shallow to deeper portions of the Tuanjiegou deposit, the mineralization is zoned from sulfide-poor quartz bands through hydrothermal breccia to deep pyrite–marcasite-rich veinlets that occur along hydrofractures within a granodiorite porphyry stock. The zoned alteration halo is centred on the ore zones, and comprises an inner phyllic alteration zone (illite + quartz + muscovite) and an outer intermediate argillic alteration zone (illite ± smectite), with propylitic alteration being limited. Given that apatite fission track ages are extremely sensitive to the ambient temperatures of 60–120 °C, the overlap in the closure dates of magmatic apatite (108.1 ± 3.8 Ma) and zircon (108.2 ± 1.2 Ma) from the granodiorite porphyry is indicative of shallow emplacement of the granodiorite porphyry, likely at depths slightly >0.7 km. A similar paleodepth (900 ± 188 m) was estimated from homogenization temperatures (291 ± 14 °C) of boiling fluids. Preservation of the deep portions of the Tuanjiegou ore system may imply that the productive ore intervals of poorly explored LS epithermal deposits globally are underestimated. Given the evidence for a magmatic origin of the ore-forming fluids at Tuanjiegou, we highlighted that ore-forming fluids are released initially from a water-saturated, oxidizing felsic melt under low-pressure (∼4 km) conditions.

Metallogenic Age and Ore‐forming Material Sources of the Dahongshan Fe‐Cu Deposit, Yunnan Province: Insights from Molybdenite Re‐Os Dating and H‐O‐S‐Pb Isotopes

AbstractThe Dahongshan Fe‐Cu (‐Au) deposit is a superlarge deposit in the Kangdian metallogenic belt, southwestern China, comprising approximately 458 Mt of Fe ores (40% Fe) and 1.35 Mt Cu. Two main types of Fe‐Cu (‐Au) mineralization are present in the Dahongshan deposit: (1) early submarine volcanic exhalation and sedimentary mineralization characterized by strata‐bound fine‐grained magnetite and banded Fe‐Cu sulfide (pyrite and chalcopyrite) hosted in the Na‐rich metavolcanic rocks; (2) late hydrothermal (‐vein) type mineralization characterized by Fe‐Cu sulfide veins in the hosted strata or massive coarse‐grained magnetite orebodies controlled by faults. While previous studies have focused primarily on the early submarine volcanic and sedimentary mineralization of the deposit, data related to late hydrothermal mineralization is lacking. In order to establish the metallogenic age and ore‐forming material source of the late hydrothermal (‐vein) type mineralization, this paper reports the Re‐Os dating of molybdenite from the late hydrothermal vein Fe‐Cu orebody and H, O, S, and Pb isotopic compositions of the hydrothermal quartz‐sulfide veins. The primary aim of this study was to establish the metallogenic age and ore‐forming material source of the hydrothermal type orebody. Results show that the molybdenite separated from quartz‐sulfide veins has a Re‐Os isochron age of 831 ± 11 Ma, indicating that the Dahongshan Fe‐Cu deposit experienced hydrothermal superimposed mineralization in Neoproterozoic. The molybdenite has a Re concentration of 99.7–382.4 ppm, indicating that the Re of the hydrothermal vein ores were primarily derived from the mantle. The δ34S values of sulfides from the hydrothermal ores are 2‰–8‰ showing multi‐peak tower distribution, suggesting that S in the ore‐forming period was primarily derived from magma and partially from calcareous sedimentary rock. Furthermore, the abundance of radioactive Pb increased significantly from ore‐bearing strata to layered and hydrothermal vein ores, which may be related to the later hydrothermal transformation. The composition of H and O isotopes within the hydrothermal quartz indicates that the ore‐forming fluid is a mixture of magmatic water and a small quantity of water. These results further indicate that the late hydrothermal orebodies were formed by the Neoproterozoic magmatic hydrothermal event, which might be related to the breakup of the Rodinia supercontinent. Mantle derived magmatic hydrothermal fluid extracted ore‐forming materials from the metavolcanic rocks of Dahongshan Group and formed the hydrothermal (‐vein) type Fe‐Cu orebodies by filling and metasomatism.

Gold mineralization related to rifting of the Rodinia surpercontinent: As gauged from the Dongyuan Au deposit, Jiangnan orogen, China

Abundant orogenic gold (Au) deposits, widely distributed in medium to low-grade metamorphic rocks, formed episodically since the Middle Archean. Orogenic Au mineralization waned during the Neoproterozoic era, although Neoproterozoic orogenies were prevalent. The Jiangnan Orogen, South China, as part of the sutures uniting the Rodinia (Meso- and Neoproterozoic) supercontinent, is situated between the Cathaysia and Yangtze blocks. Many orogenic Au deposits, such as the Wan’gu, Huangjindong, Dongyuan, and Jinshan Au deposits, are located in the northeastern section of the Jiangnan Orogen. The orebodies of the recently discovered Dongyuan deposit display a horizontal zonation, as follows: a peripheral quartz–chlorite–sulfide–calcite (ankerite, manganocalcite, and calcite) veinlets/veins and a central sulfide (mainly arsenopyrite) veinlets/veins. The former veinlets/veins also contain a small amount of albite, scheelite, TiO2 minerals, xenotime, and monazite. Compared with the other orogenic Au deposits, arsenopyrite from the Dongyuan Au deposit is characterized by enrichment of Sb–Co–Cd–Ag element assemblages. Based on the electron microprobe and Raman analyses, TiO2 mineral grains, including anatase, rutile, and anatase–rutile intergrowths, are present in the Au veins. In contrast with previous studies, TiO2 minerals (anatase and rutile) have a nearly consistent concentration range of each element detected, which taken together can be used for constraining fluid sources of ores. TiO2 minerals with enriched V–Fe assemblages, combined with initial 187Os/188Os ratio (0.64 ± 0.11) of arsenopyrite, reflect that the Dongyuan Au veins were probably precipitated from a metamorphic fluid. The Liyangdou biotite granodiorite and Donggang granite, located about one kilometer north and six kilometers south of the deposit, have LA-ICP-MS U–Pb zircon ages of 803 ± 3.4 Ma and 814 ± 3.4 Ma, respectively. The analysis of five arsenopyrite samples selected from the Dongyuan Au veins yields an isochron age of 744 ± 36 Ma (with an initial 187Os/188Os ratio of 0.64 ± 0.11 (2σ) and MSWD = 30). We found that the Dongyuan Au mineralization was later than the peripheral Neoproterozoic magmatic activities and metamorphic events of country rocks. Combined with previous studies, the Dongyuan deposit was formed in the tectonic setting of Rodinia supercontinent rifting, after the Neoproterozoic collision event in the Jiangnan Orogen, which likely triggered orogenic Au mineralization.

Visible-light-driven Au/PCN-224/Cu(II) modified fabric with enhanced photocatalytic antibacterial and degradation activity and mechanism insight

The development of novel photocatalytic platform for efficient water purification and sterilization is of utmost importance due to the significant threat of chronic diseases resulting from water pollution and bacterial contamination. Herein, a high-efficiency, easy-recyclable, and environment-friendly photocatalytic fabric was developed as a water disinfection and organic pollutant degradation platform. In which, microamounts of Au nanoparticles (2 wt%) and Cu(II) clusters (2.5 wt%) co-decorated porphyrinic MOF (Au/PCN-224/Cu(II)) coating was applied as photocatalytic surface, and flexible cotton fabric served as stable support. Au/PCN-224/Cu(II) composite photocatalyst was prepared via a facile photo-deposition procedure followed by impregnation method, and further immobilized onto polydopamine (PDA) pre-treated cotton fabric through catechol-amine reaction. The fabricated photocatalytic platform exhibited excellent ability to generate reactive oxygen species (ROS) by multiple routes under low-power visible light irradiation, and achieved efficient photodisinfection effects for causative organism including Gram-negative Escherichia coli (E. coli) and Gram-positive Staphylococcus aureus (S. aureus) without the obvious leakage of metal ions from the potocatalyst during the reaction. Additionally, the reaction rate constant for organic dye MB photodegradation achieved by Au/PCN-224/Cu(II)@Fabric was 3.73 times higher than that of PCN-224@Fabric, and the degradation intermediates analysis was also conducted. The band alignments of PCN-224, Au/PCN-224, Au/PCN-224/Cu(II) photocatalysts were determined, and the charge transfer mechanism within Au/PCN-224/Cu(II) photocatalyst was elucidated through the utilization of DRS, Mott − Schottky, ESR, EIS, and photocurrent analyses. It is suggested that the deposition of Au and doping of Cu(II) both with small amounts enhanced the light absorption capacity, and also improved the charge separation ability through the surface plasmon resonance (SPR) effect and interfacial electron transfer (IFCT) mechanism. Moreover, Au SPR and Cu doping exhibited a substantial enhancement in photothermal conversion effect, thereby synergistically reinforcing the sterilization performance. This work provides an approach for the development of effective photocatalytic platform based on porphyrinic MOFs combined with trace metal co-catalysts in the application of water disinfection and purification.

Ore deposit prospecting using the chlorine and bromine secondary dispersion halos

The Cland Brions, that form complex compounds with metals, produce secondary dispersion halos in the hypergenesis zone at Au, Ag, Cu, Pb, and Zn ore deposits which ore bodies are controlled by fracturing and fault structures. The appearance of anomalies of the highly mobile water-soluble ions, manifested on the surface and in the wall rocks, is explained by their transfer from the deep sources to the surface by a gas flow. The migration of the ions to the earth's surface and further into the atmosphere is influenced by many factors (atmospheric pressure, temperature, humidity, rock porosity, etc.) that complicate the observation results.

Cathodoluminescence and geochemical characteristics of Apatite: Implications for mineral exploration in the Xiongcun District, Tibet, China

Apatite grains from the No. 2 porphyry Cu–Au deposit in the Xiongcun district of Tibet, China, have a range of physical and compositional features. This study investigates the potential use of apatite associated with hydrothermal alteration as a tool for mineral exploration. In situ textural, cathodoluminescence (CL), and chemical analyses were performed on thin sections containing apatite from various alteration zones in the deposit. No clear variation was seen in apatite from rocks of the potassic, sodic–calcic, chlorite–sericite, phyllic, and propylitic alteration zones using visible light and scanning electron microscopy; however, distinct variations were observed in optical cathodoluminescence (OP-CL) (dark yellow to green, orange to green, yellow–brown to green, yellow-orange to brown, and light yellow–brown to green luminescence for the respective zones). The alteration-related differences in luminescence were a result of the interaction between Fe and Mn; the Na and Cl contents; and depletion in total heavy rare earth elements (ΣHREE) and Y. The variations in the REE contents of apatite from different types of altered rock record reactions with Cl- and F-rich fluids. The partitioning behavior of Cl between apatite and hydrothermal fluids is influenced by pressure, temperature, pH, and fluid composition, whereas the partitioning of F between apatite and fluids is dependent on the fluid composition and not the temperature. At high temperatures, Eu3+ is reduced to Eu2+, which results in negative Eu anomalies in apatite from the potassic-altered rocks and propylitic-altered rocks. Apatite grains in the sodic–calcic-altered rocks and chlorite–sericite-altered rocks show a similar enrichment in light REEs (LREEs) that resulted from REE and Y incorporation as follows: Na+ + (Y + REE)3+ = 2Ca2+. Apatite grains in the phyllic-altered rocks are enriched in the middle REEs. This study confirms that the luminescence, chemical composition (including Fe, Mn, Na, Cl, ΣHREE, and Y contents), and REE patterns of apatite can be affected by hydrothermal alteration; therefore, these results may be used to constrain the evolution of ore-forming hydrothermal fluids and may offer an effective tool for mineral exploration.