Search Results (11)

Active and abandoned mining sites are significant sources of heavy metals and metalloid pollution, leading to serious environmental issues. This study assessed the environmental risks posed by potentially toxic elements (PTEs), specifically arsenic (As) and antimony (Sb), in the Technosols (mining residues) of the former Pejão coal mine complex in Northern Portugal, a site impacted by forest wildfires in October 2017 that triggered underground combustion within the waste heaps. Our methodology involved determining the “pseudo-total” concentrations of As and Sb in the collected heap samples using microwave digestion with aqua regia (ISO 12914), followed by analysis using hydride generation-atomic absorption spectroscopy (HG-AAS). The concentrations of As an Sb ranging from 31.0 to 68.6 mg kg⁻¹ and 4.8 to 8.3 mg kg⁻¹, respectively, were found to be above the European background values reported in project FOREGS (11.6 mg kg⁻¹ for As and 1.04 mg kg⁻¹ for Sb) and Portuguese Environment Agency (APA) reference values for agricultural soils (11 mg kg⁻¹ for As and 7.5 mg kg⁻¹ for Sb), indicating significant enrichment of these PTEs. Based on average I_geo values, As contamination overall was classified as “unpolluted to moderately polluted” while Sb contamination was classified as “moderately polluted” in the waste pile samples and “unpolluted to moderately polluted” in the downhill soil samples. However, total PTE content alone is insufficient for a comprehensive environmental risk assessment. Therefore, further studies on As and Sb fractionation and speciation were conducted using the Shiowatana sequential extraction procedure (SEP). The results showed that As and Sb levels in the more mobile fractions were not significant. This suggests that the enrichment in the burned (BCW) and unburned (UCW) coal waste areas of the mine is likely due to the stockpiling of lithic fragments, primarily coals hosting arsenian pyrites and stibnite which largely traps these elements within its crystalline structure. The observed enrichment in downhill soils (DS) is attributed to mechanical weathering, rock fragment erosion, and transport processes. Given the strong association of these elements with solid phases, the risk of leaching into surface waters and aquifers is considered low. This work underscores the importance of a holistic approach to environmental risk assessment at former mining sites, contributing to the development of sustainable remediation strategies for long-term environmental protection. Full article

The Zhen’an-Xunyang Basin is a late Paleozoic rifted basin with a series of Au-Hg-Sb deposits that have been found, mostly along the Nanyangshan fault. Recently discovered large- and medium-sized gold deposits such as the Xiaohe and Wangzhuang deposits exhibit typical characteristics of Carlin-type gold deposits. Therefore, it is imperative to select a typical deposit for an in-depth study of its metallogenic mechanism to support future prospecting efforts targeting the Carlin-type gold deposits within the area. Based on detailed field investigation and microphotographic observation, four ore-forming stages are identified: I, low-sulfide quartz stage, characterized by euhedral, subhedral pyrite, and fine veins of quartz injected parallel to the strata; II, arsenopyrite–arsenian pyrite–quartz stage, the main mineralization stage characterized by strongly silicified zones of reticulated quartz, disseminated arsenopyrite, fine-grained pyrite; III, low-sulfide quartz stage, characterized by large quartz veins cutting through the ore body or fine veins of quartz; Ⅳ, carbonate–quartz stage, characterized by the appearance of a large number of calcite veins. In situ analysis of trace elements and S isotopes of typical metal sulfides was carried out. The results show significant variations in the trace element compositions of metal sulfides in different stages, among which the main mineralization stage differs notably from those of the Au- and As-low surrounding strata. In situ S isotope analysis reveals δ³⁴S values ranging from 15.78‰ to 28.71‰ for stage I metal sulfides, 5.52‰ to 11.22‰ for stage II, and 0.3‰ to 5.25‰ for stage III, respectively, revealing a gradual decrease in S isotopic values from the pre-mineralization stage to post-mineralization stage, similar to those observed in the Xiaohe gold deposit. These features indicate a distinct injection of relatively low ³⁴S hydrothermal fluids during the mineralization process. The element anomalies of the 1:50,000 stream sediment in the region revealed ore-forming element zonation changing in W→Au (W)→Hg, Sb (Au) anomalies from west to east, manifested by the discovery of tungsten, gold, and mercury–antimony deposits in the area. Moreover, conspicuous Cr-Ni-Ti-Co-Mo anomalies were observed on the western side of the Wangzhuang and Xiaohe gold deposits, indicating a potential concealed pluton related to these deposits. These lines of evidence point to a magmatic–hydrothermal origin for the Carlin-type gold deposits in this area. Furthermore, hydrothermal tungsten deposits, Carlin-type gold deposits, and low-temperature hydrothermal mercury–antimony deposits in this region are probably controlled by the same magma–hydrothermal system. Full article

The Nanpanjiang basin hosts the world’s second-largest concentration of Carlin-type gold deposits. To decipher the origin and evolution of hydrothermal fluid, this study conducted Sm–Nd dating, in-situ trace element, and C-O-Sr isotopic analyses on three types of calcite samples from the giant Lannigou gold deposit in the Nanpanjiang basin, SW China. The type-I calcite, intergrown with Au-bearing arsenian pyrite, has an Sm–Nd isochron age of 213 ± 7 Ma (MSWD = 0.81), indicating that gold mineralization occurred in Late Triassic. The type-II calcite, which coexists with high-maturity bitumens and cut through the main-stage gold orebodies, yields an Sm–Nd age of 188 ± 14 Ma (MSWD = 0.34), representing a post-ore hydrocarbon accumulation event. The type-I and type-II calcite samples have low REE contents (5.28–51.6 ppm) and exhibit MREE-enriched and LREE-/HREE-depleted patterns. Combined with their identical C-O-Sr isotopes, we suggest that hydrothermal fluids responsible for the precipitation of type-I and type-II calcite samples were derived from a mixed metamorphic fluid and meteoric water source. In contrast, the type-III calcite samples, associated with realgar and orpiment, have distinct Mn, Sr, and As contents, REE patterns, and C-O-Sr isotopic composition from the type-I and II calcites, suggestive of different fluid sources. Based on our and previously published data, we propose that the fluid evolution, gold mineralization, and hydrocarbon accumulation in the Nanpanjiang basin are closely related to the Indosinian and Yanshanian orogenies in South China. Full article

The Golden Ridge gold deposit is located in southwestern New Brunswick, in the Canadian Appalachians. Gold mineralization is consistently associated with acicular arsenopyrite, and to a lesser degree with pyrite, disseminated in host rocks, sulphide veinlets, quartz-carbonate veins, and the breccia matrix. According to petrographic-based textural differences, four types of pyrite and two types of arsenopyrite are recognized with associated assemblages. Based on SEM-BSE imaging and LA-ICP-MS spot analyses of the different types of pyrites and arsenopyrites, “invisible gold” (solid solution in the crystal lattice of pyrite and arsenopyrite or <100 nm nanoparticles) and micrometer-size inclusions were identified as the main forms of Au. Four syn-gold mineralization pulses of fluid are suggested. The initial hydrothermal fluid, which generated low-grade pyrite (Py-I) enriched in Sb, Pb, Cu, Co, Ni, and Bi, was followed by a second pulse of fluid enriched in arsenic and gold, generating coprecipitated Py-II and Asp-I. The third and fourth pulses were enriched in both arsenic and gold and precipitated Py-III, then coprecipitated Py-IV and Asp-II, which constitute the most important Au depositional episodes. The repeated occurrence of growth zones with Au enrichment in the arsenian pyrites (Py-II, Py-III, and Py-IV) indicate surface growth during metal deposition and disequilibrium crystallization processes. Full article

The Yana–Kolyma metallogenic belt, NE Russia, is a world-class gold belt with resources numbering ~8300 tons of gold. The belt is localized in the central part of the Verkhoyansk–Kolyma orogen, formed by a collage of diverse terranes. The Tithonian-to-Early-Cretaceous orogenic gold deposits are hosted in a sequence of Permian–Triassic and Jurassic clastic rocks and altered Late Jurassic andesite, dacite, granodiorite, trachyandesite, and trachybasalt dykes. High-fineness gold (800–900‰) in quartz veins and invisible gold in disseminated arsenian pyrite-3 (Py3) and arsenopyrite-1 (Apy1) are present in ores. Here, we present new data about microtextures; the chemical composition and stable sulfur isotopes of auriferous pyrite-3 and arsenopyrite-1 from proximal alterations in sediment-hosted (Malo–Taryn, Badran, Khangalas); and intrusion-hosted (V’yun, Shumniy) orogenic Au deposits in the central sector of the Yana–Kolyma metallogenic belt to better constrain the ore-forming process and tracking their evolution. Detailed petrography defined the following generations of pyrite: syn-sedimentary/diagenetic Py1, metamorphic Py2 and hydrothermal Py3, and Apy1. Hydrothermal Py3 and Apy1 are localized in the proximal pyrite–arsenopyrite–sericite–carbonate–quartz alteration in ore zones and make a major contribution to the economic value of the veinlet-disseminated mineralization with “invisible” gold in the orogenic deposits of the Yana–Kolyma metallogenic belt. Electron microprobe analysis (EMPA) of Py3 in both types of deposits shows concentrations of As (up to 3.16 wt%), Co, Ni, Cu, Sb, and Pb. Py3 in intrusion-hosted orogenic gold deposits reveals elevated concentrations of Co (up to 0.87 wt%), Ni (up to 3.52 wt%), and Cu (up to 2.31 wt%). The identified negative correlation between S and As indicates an isomorphic substitution of sulfur by As¹⁻. Py3 from igneous rocks is characterized by a high degree of correlation for the pairs Fe²⁺→ Co²⁺ and Fe²⁺→ Ni²⁺. For hydrothermal Apy1, Co (up to 0.27 wt%), Ni (up to 0.30 wt%), Cu (up to 0.04 wt%), and Sb (up to 0.76 wt%) are typomorphic. According to atomic absorption spectrometry, the concentration of Au in Py3 reaches 159.5 ppm; in Apy1, it reaches 168.5 ppm. The determination of the precise site of the invisible gold within Py3 and Apy1 showed the predominance of solid-solution Au⁺ in the crystal lattice. The values of δ³⁴S in Py3 and Apy1 (from −6.4 to +5.6‰, mean value of about +0.6‰), both from sediment-hosted and from intrusion-hosted deposits, display a relatively narrow range and are characteristic of the hydrothermal ore stage. Our analytical results showed no systematic differences between the chemical and stable sulfur isotope compositions of both auriferous pyrite-3 and arsenopyrite-1 from the proximal alteration in sediment-hosted (Malo–Taryn, Badran, Khangalas) and intrusion-hosted (V’yun, Shumniy) orogenic Au deposits, indicating that the primary source of sulfur, gold, and mineralizing fluids was likely from subcrustal and metamorphic systems in the Late-Jurassic-to-Early-Cretaceous Verkhoyansk–Kolyma orogen. Full article

Pumping groundwater from arsenic (As)-contaminated aquifers exposes millions of people, especially those in developing countries, to high doses of the toxic contaminant. Previous studies have investigated cost-effective techniques to remove groundwater arsenic by stimulating sulfate-reducing bacteria (SRB) to form biogenic arsenian pyrite. This study intends to improve upon these past methods to demonstrate the effectiveness of SRB arsenic remediation at an industrial site in Florida. This study developed a ferrous sulfate and molasses mixture to sequester groundwater arsenic in arsenian pyrite over nine months. The optimal dosage of the remediating mixture consisted of 5 kg of ferrous sulfate, ~27 kg (60 lbs) of molasses, and ~1 kg (2 lbs) of fertilizer per 3785.4 L (1000 gallons) of water. The remediating mixture was injected into 11 wells hydrologically upgradient of the arsenic plume in an attempt to obtain full-scale remediation. Groundwater samples and precipitated biominerals were collected from June 2018 to March 2019. X-ray diffraction (XRD), X-ray fluorescence (XRF), electron microprobe (EMP), and scanning electron microscope (SEM) analyses determined that As has been sequestered mainly in the form of arsenian pyrite, which rapidly precipitated as euhedral crystals and spherical aggregates (framboids) 1–30 μm in diameter within two weeks of the injection. The analyses confirmed that the remediating mixture and injection scheme reduced As concentrations to near or below the site’s clean-up standard of 0.05 mg/L over the nine months. Moreover, the arsenian pyrite contained 0.03–0.89 weight percentage (wt%) of sequestered arsenic, with >80% of groundwater arsenic removed by SRB biomineralization. Considering these promising findings, the study is close to optimizing an affordable procedure for sequestrating dissolved As in industry settings. Full article

The Zn-Pb ores of the Castellanos shale-hosted, clastic-dominated deposit in northwest Cuba average nearly 1 g/t Au, with local maximum concentrations up to 34 g/t Au. This deposit is stratiform with respect to the bedding in the host black shales and shows a bottom to top zoning of ore assemblages made up of a stockwork underlying the main orebody, a basal pyrite-rich zone and a disseminated to massive Zn-Pb ore zone capped by a discontinuous, thin barite-rich zone. Petrographic data and textural relations allow distinguishing five textural types of pyrite (framboidal Py I, colloform Py IIa, euhedral Py IIb, massive Py IIc and banded colloform Py III) successively formed during ore deposition. The main Zn-Pb ore formed after the crystallization of disseminated, sedimentary framboidal pyrite (Py I) in black shales by the superimposition of several crystallization events. The crystallization sequence of the main ore-forming stage evolved from the precipitation of colloform sphalerite and pyrite (Py IIa) with skeletal galena and interstitial dolomite-ankerite to similar ore assemblages but showing subhedral to euhedral crystal habits (Py IIb) and interstitial calcite-rich carbonates. This stage ended with the development of massive pyrite (Py IIc), mainly occurring at the base of the stratiform orebody. A late fracturing stage gave way to the development of a new generation of colloform banded pyrite (Py III) just preceding the crystallization of early barite. Au is mainly concentrated in pyrite showing variable contents in the different textural types of pyrite and a bottom to top enrichment trend. Minimum contents occur in massive pyrite (Py IIc) from the basal pyrite-rich zone (0.18 ppm Au average), increasing in pyrite IIa (from 0.29 to 2.86 ppm Au average) and in euhedral pyrite (Py IIb) (from 0.82 to 9.02 ppm Au average), reaching maxima in colloform banded pyrite (Py III) formed just before the crystallization of early barite at the top of the orebody. Au enrichment in pyrite correlates with that of Sb (0.08–4420 ppm), As (0.7–35,000 ppm), Ag (0.03–1560 ppm) and to a lesser extent Cu (3–25,000 ppm), Ni (0.02–1600 ppm) and Mn (0.6–5030 ppm). Au deposition should have taken place by oxidation and, probably cooling, of reduced (H₂S-dominated) fluids buffered by organic matter-rich black shales of the host sedimentary sequence. The input of such reduced fluids in the ore-forming environment most probably occurred alternating with that of the main oxidized fluids which leached Zn and Pb from the large volume of sandstones and siltstones making up the enclosing sequence, thus being responsible for the precipitation of the majority Zn-Pb ore. Supply of Au-carrying reduced fluids might progressively increase over the course of ore formation, reaching a maximum at the beginning of the late fracturing stage. This evolution of Au supply is consistent with the early crystallization of barite since Ba can also only be transported at low temperature by highly reduced fluids. These results highlight the potential of medium-sized, shale-hosted, clastic-dominated deposits to contain economic (by product) Au amounts and show that ore-forming fluids can change from oxidized (SO₄²⁺ dominated) to reduced (H₂S-dominated), and vice versa, throughout the evolutionary history of a single deposit. Full article

Active, shallow-water (2–10 m below sea level) and low temperature (up to 115 °C) hydrothermal venting at Paleochori Bay, nearshore Milos Island, Greece, discharges CO₂ and H₂S rich vapors (e.g., low-Cl fluid) and high-salinity liquids, which leads to a diverse assemblage of sulfide and alteration phases in an area of approximately 1 km². Volcaniclastic detritus recovered from the seafloor is cemented by hydrothermal pyrite and marcasite, while semi-massive to massive pyrite-marcasite constitute mounds and chimney-like edifices. Paragenetic relationships indicate deposition of two distinct mineralogical assemblages related to the venting of high-Cl and low-Cl fluids, respectively: (1) colloform As- and Hg-bearing pyrite (Py I), associated with marcasite, calcite, and apatite, as well as (2) porous and/or massive As-rich pyrite (Py II), associated with barite, alunite/jarosite, and late-stage hydrous ferric oxides. Mercury, in the form of cinnabar, occurs within the As-rich pyrite (Py I) layers, usually forming distinct cinnabar-enriched micro-layers. Arsenic in colloform pyrite I shows a negative correlation with S indicating that As¹⁻ dominates in the pyrite structure suggesting formation from a relatively reducing As-rich fluid at conditions similar to low-sulfidation epithermal systems. On the contrary, As³⁺ dominates in the structure of porous to massive pyrite II suggesting deposition from a sulfate-dominated fluid with lower pH and higher fO₂. Bulk sulfide data of pyrite-bearing hydrothermal precipitates also show elevated As (up to 2587 ppm) together with various epithermal-type elements, such as Sb (up to 274 ppm), Tl (up to 513 ppm), and Hg (up to 34 ppm) suggesting an epithermal nature for the hydrothermal activity at Paleochori Bay. Textural relationships indicate a contemporaneous deposition of As and Hg, which is suggested to be the result of venting from both high-salinity, liquid-dominated, as well as CO₂- and H₂S-rich vapor-dominated fluids that formed during fluid boiling. The CO₂- and H₂S-rich vapor that physically separated during fluid boiling from the high-salinity liquid led to calcite formation upon condensation in seawater together with the precipitation of As- and Hg-bearing pyrite I. This also led to the formation of sulfuric acid, thereby causing leaching and dissolution of primary iron-rich minerals in the volcaniclastic sediments, finally resulting in pyrite II precipitation in association with alunite/jarosite. The Paleochori vents contain the first documented occurrence of cinnabar on the seafloor in the Mediterranean area and provide an important link between offshore hydrothermal activity and the onshore mercury and arsenic mineralizing system on Milos Island. The results of this study therefore demonstrate that metal and metalloid precipitation in shallow-water continental arc environments is controlled by epithermal processes known from their subaerial analogues. Full article

The Goldstrike district in southwest Utah is similar to Carlin-type gold deposits in Nevada that are characterized by sediment-hosted disseminated gold. Suitable structural and stratigraphic conditions facilitated precipitation of gold in arsenian pyrite grains from ascending gold-bearing fluids. This study used ground-based hyperspectral imaging to study a core drilled in the Goldstrike district covering the basal Claron Formation and Callville Limestone. Spectral modeling of absorptions at 2340, 2200, and 500 nm allowed the extraction of calcite, clay minerals, and ferric iron abundances and identification of lithology. This study integrated remote sensing and geochemistry data and identified an optimum stratigraphic combination of limestone above and siliciclastic rocks below in the basal Claron Formation, as well as decarbonatization, argillization, and pyrite oxidation in the Callville Limestone, that are related with gold mineralization. This study shows an example of utilizing ground-based hyperspectral imaging in geological characterization, which can be broadly applied in the determination of mining interests and classification of ore grades. The utilization of this new terrestrial remote sensing technique has great potentials in resource exploration and exploitation. Full article

The Shuiyindong Gold Mine hosts one of the largest and highest-grade, strata-bound Carlin-type gold deposits discovered to date in Southwestern China. The outcrop stratigraphy and drill core data of the deposit reveal Middle–Upper Permian and Lower Triassic formations. The ore is mainly hosted in Upper Permian bioclastic limestone near the axis of an anticline. The gold is mainly hosted in arsenian pyrite and arsenopyrite, mainly existing in the form of crystal lattice gold, submicroscopic particles and nanoparticles. Fluorite commonly occurs at the vicinity of an unconformity between the Middle–Upper Permian formations, which is proposed to be the structural conduit that fed the ore fluids. Calcite commonly fills fractures at the periphery of decarbonated rocks, which contain high grade orebodies. This study aimed to verify the occurrence of two distinct hydrothermal events at the Shuiyindong, based on Sm–Nd isotope dating of the fluorite and calcite. For this purpose, rare-earth element (REE) concentrations, Sm/Nd isotope ratios, and Sm–Nd isochron ages of the fluorite and calcite were determined. The fluorite and calcite contain relatively high total concentrations of REE (12.3–25.6 μg/g and 5.71–31.7 μg/g, respectively), exhibit variable Sm/Nd ratios (0.52–1.03 and 0.57–1.71, respectively), and yield Sm–Nd isochron ages of 200.1 ± 8.6 Ma and 150.2 ± 2.2 Ma, with slightly different initial ${\mathsf{\epsilon }}_{\mathrm{Nd}}\left(\mathrm{t}\right)$ values of −4.4 and −1.1, respectively. These two groups of Sm–Nd isochron ages suggest two episodes of hydrothermal events at the Shuiyindong gold deposit. The age of the calcite probably represents the late stage of the gold mineralization period. The initial ${\mathsf{\epsilon }}_{\mathrm{Nd}}\left(\mathrm{t}\right)$ values of the fluorite and calcite indicate that the Nd was probably derived from mixtures of basaltic volcanic tuff and bioclastic limestone from the Permian formations. Full article

The Zhengchong gold deposit is located in the central segment of the Jiangnan Orogen in northeastern Hunan Province, South China. The host rocks of this deposit are the Neoproterozoic slates of the Lengjiaxi Group and granodiorite. The structures in the Zhengchong gold deposit are dominated by NE-trending reverse faults, which control the gold-bearing veins. The orebody consists of NE-trending laminated quartz veins and NW-trending quartz veins. The alteration styles include silicification, carbonatization, sulfidation, sericitization and chloritization. The Zhengchong gold mineralization can be divided into four stages: Quartz-pyrite (stage I), quartz-pyrite-arsenopyrite (stage II), quartz-polysulfide (stage III) and quartz-carbonate (stage IV). Three generations of hydrothermal pyrite were identified: Disseminated euhedral to subhedral cubes in altered wall-rock (PyI), euhedral to subhedral cubes inter-grown with arsenopyrite and tetrahedrite in quartz veins and wall-rock (PyII), and euhedral cubes with microinclusions (native gold, galena, sphalerite, chalcopyrite, tetrahedrite, and pyrrhotite) or metasomatic textures in sulfide-rich veins or veinlets (PyIII). PyII and PyIII are arsenian pyrite and represent the main Au-bearing minerals. PyI records the lowest concentrations of Au; PyII and PyIII record similar amounts of Au, Cu, Pb, Zn, and Bi, but PyIII is more enriched in Co, Ni, Te, and Se. The substitution of As, Se and Te for S and that of Co and Ni for Fe occurs by direct-ion exchange. Invisible gold is uniformly distributed within the arsenian pyrite, and visible gold fills microfractures in PyII or occurs as inclusions in PyIII. Co, Ni, Cu exhibit positive correlations with Au and a negative correlation between Au + Cu + Co + Ni and Fe reflect that Fe vacancies may have been a major cause of the precipitation of invisible Au and other metal elements in pyrite structure. There are systematic trace element differences between the three generations of pyrite (PyI, PyII, PyIII). The more Co, Ni and Se, Te substitution that occurred for Fe and S, respectively, the greater the increase in the Co/Ni ratio (<1) and the decrease in the Se/Te ratio (<10) in stage III, indicating that a more reduced, lower-temperature metamorphic hydrothermal fluid was present in stage III. Full article