Search Results (762)

The evaluation of potentially toxic element concentrations (PTEs) in soils and plants is essential for understanding environmental quality and potential human exposure in areas affected by intense anthropogenic activity. This study addresses a research gap in the Valencian Region, focusing on soil–plant interactions of PTEs in urban and industrial environments. We assess the status of the soil–plant system in a region of the Valencian Community (eastern Spain) subjected to strong urban, industrial and agricultural pressure. A total of 55 soil samples and 47 plant samples were collected from agricultural, urban and industrial sites and analysed for soil properties, major elements (Al, Mg, Fe) and PTEs (As, Cd, Co, Cr, Cu, Li, Mn, Ni, Sr, V and Zn). Land use significantly influenced soil physicochemical characteristics, with clear differentiation among environments. Soil texture and organic matter were the main factors controlling element retention, while Al, Fe and Mg dominated the geochemical composition, consistent with Mediterranean calcareous soils. Correlation analyses revealed strong co-occurrence patterns among lithogenic elements (e.g., Fe-Al, r = 0.917 p < 0.01), soil texture and chemical properties, indicating a shared origin and preferential retention in the fine fraction and soil organic matter. Contamination indices identified potential environmental risk mainly associated with Cu, Pb, Sr and Zn, particularly in densely populated areas. Mean concentrations of Cd, Cr, Cu, Pb and Zn were, respectively, 0.63 mg kg⁻¹, 42.25 mg kg⁻¹, 31.49 mg kg⁻¹, 56.91 mg kg⁻¹ and 76.08 mg kg⁻¹. These elements exceeded Spanish regulatory reference values in several soils. Bioaccumulation indices indicated notable plant uptake of As, Sr and Zn, highlighting their potential for trophic transfer. Full article

The Xiangshan ore field is characterized by extensive alkali metasomatism, which represents the early-stage hydrothermal event before the acidic metasomatism during major U mineralization. However, the mineralogical and geochemical characteristics of alkali metasomatism, as well as its association with uranium mineralization, remain poorly understood. This study evaluates these scientific problems by conducting petrographic and geochemical analyses on feldspar, together with thermodynamic modeling. Hydrothermal feldspars are present as veinlets, differing from the magmatic ones with granular and subhedral structures. Hydrothermal albites have lower Na but higher K content than magmatic ones, while hydrothermal K-feldspars have lower K but higher Na content than magmatic ones. In addition, hydrothermal feldspars are significantly depleted in Ca and Sr, likely associated with the consumption of Ca in fluids by fluorite and calcite precipitation. Furthermore, alkali metasomatism is accompanied by intense hematitization, indicating the oxidized properties of ore fluids that are favorable for uranium transport. Thermodynamic modeling further demonstrates that continuous K⁺ consumption during fluid–rock interaction leads to a pH increase in the fluid, which is buffered by quartz–muscovite–K-feldspar (QMF). Given that quartz solubility is positively correlated with pH, this process induces extensive quartz dissolution in the host rocks. Such dissolution significantly enhances the porosity and permeability of the host rocks, creating ideal physical traps for the subsequent accumulation of uranium-bearing fluids. Consequently, alkali-metasomatized rocks associated with quartz dissolution and hematitization serve as critical indicators for regional uranium exploration. Full article

The Mahu Sag, a hydrocarbon-rich depression within the Junggar Basin, hosts significant petroleum resources. Here, the Permian Fengcheng Formation shale oil reservoirs have emerged as a primary exploration target. This study investigates fracture development within these alkaline lacustrine shales, a critical factor governing hydrocarbon migration and accumulation. Through integrated petrographic and geochemical analyses, we elucidate a multifactorial fracture formation mechanism driven by the interplay of alkaline minerals, stress, and fluids. Two distinct fracture types were identified: bedding-complex fracture veins (BCFVs) and Y-shaped high-angle fracture veins (Y-HFVs). Both fracture types result from alkaline fluid–rock interactions, which induce fracture opening along specific orientations, alter fracture angles, and control aperture width and final morphology. Alkaline mineral assemblages further influence fracture evolution via dissolution–precipitation cycles. Concurrently, these assemblages preserve hydrocarbons by inhibiting the thermal maturation of organic matter, as evidenced by variations in fluid inclusion fluorescence. The fracture networks act as crucial migration pathways, with the BCFV containing higher-maturity hydrocarbons (indicated by blue-green fluorescence) and the Y-HFV retaining less mature fluids (indicated by yellow-green fluorescence). This study presents the first systematic characterization of the multifactorial controls on fractures in alkaline lake environments, proposing a cooperative “alkaline minerals–stress–fluids” mechanism. These findings provide a new framework for understanding fracture development in alkaline lacustrine shales and offer valuable insights for shale oil exploration in analogous depositional settings. Full article

Revitalisation of contaminated brownfield sites is essential for sustainable development, particularly near sensitive ecological areas like Natura 2000 sites. The lagoon in Slovenia’s Regional Park Šturmovci, an artificial wastewater convergence point created during hydroelectric construction, is a highly relevant example. This study integrates geochemical, mineralogical and isotopic analyses to identify sources and controlling mechanisms of contaminant distribution in lagoon sediments and assess their transfer to nearby agricultural soils during flooding events. Results indicate anaerobic conditions, with depth-related shifts in phosphorus, sulphur and redox-sensitive elements, such as rare earth elements (REE), arsenic (As), barium (Ba), cobalt (Co), chromium (Cr), lead (Pb) and vanadium (V), as well as fluctuations in pyrite-rich laminated layers, suggesting potential flood-driven remobilisation of trace elements. Lagoon sediments are highly contaminated with As (73 mg kg⁻¹), Ba (247 mg kg⁻¹), Pb (97 mg kg⁻¹) and Zn (1118 mg kg⁻¹), with elevated concentrations also observed in agricultural soil, all exceeding respective limit values of 20, 160, 85 and 200 mg kg⁻¹. Pollutant concentrations were highest near wastewater inflows and decreased with distance, with nitrogen isotopic patterns indicating partial nitrification and surface ammonium accumulation, reflecting intensive agricultural inputs in the area. High enrichment factor (EF > 20) and geoaccumulation index (I_geo > 3) values, in particular for As, Cd and Zn, indicated severe contamination and highlighted the urgent need for effective remediation strategies, including immobilisation using biochar or cement-based binders, as well as phytoremediation approaches. Full article

Plants of the genus Salacia (Celastraceae) have long been used in traditional medical systems of South and Southeast Asia for the management of diabetes and related metabolic disorders. Modern phytochemical and pharmacological studies have confirmed the antidiabetic potential of several Salacia species, leading to the identification of a distinctive group of sulfur-containing sugars as their principal bioactive constituents. Salacinol, neosalacinol, kotalanol, neokotalanol, and related analogues represent a novel class of thiosugar sulfonium compounds that act as potent and selective α-glucosidase inhibitors, providing a clear mechanistic basis for their glucose-lowering effects. Simpler thiosugars, such as 5-thiomannose, further contribute to the overall metabolic activity of Salacia extracts and may serve as biosynthetic or functional precursors. Beyond Salacia, sulfur-containing natural products are widespread in nature and perform diverse biological roles. In particular, the genus Allium is well known for producing organosulfur compounds, including thioethers and polysulfides, which exhibit antidiabetic, hypolipidemic, antioxidant, and cardioprotective activities. In a different context, sulfur-containing hopanes have been identified in sediments and petroleum as products of early diagenetic sulfurization of bacterial hopanoids. Although these compounds have been studied primarily as geochemical biomarkers, recent QSAR/PASS analyses suggest that sulfur hopanes may also possess biologically relevant activities, particularly related to metabolic and cardiovascular regulation. Recent PASS-based QSAR evaluations of Salacia-derived thiosugars and sulfur hopanes predict significant antidiabetic activity, including potential type 2 diabetes-related pharmacological effects, supported by predicted α-glucosidase inhibitory, hypoglycemic, hepatic, and gastrointestinal activities. Collectively, these findings highlight sulfur-containing natural products from both plant and sedimentary sources as chemically diverse yet functionally convergent scaffolds with promising potential for the development of functional foods and therapeutic agents targeting metabolic disorders. Full article

The Huoyanshan Cu-Zn volcanogenic massive sulfide (VMS) deposit, located in the North Qilian Orogenic Belt, China, is of significant economic importance. This study provides new constraints on the ore-forming processes through high-resolution in situ trace element and sulfur isotope analyses of pyrite and sphalerite using LA-(MC)-ICP-MS. Petrographic and geochemical investigations identified three distinct generations of pyrite (Py l to Py III). Early-stage Py I and Py II are characterized by high trace element contents (Au, As, Bi, Cu, Pb), elevated Co/Ni ratios (>1–10), and enriched δ³⁴S values (+4.98‰ to +7.47‰). These signatures indicate precipitation from high-temperature, reduced magmatic–hydrothermal fluids influenced by thermochemical sulfate reduction (TSR). Late-stage Py IIl exhibits markedly lower Co/Ni ratios (<0.1) and lighter δ³⁴S values (+3.72‰ to 3.89‰). This geochemical shift reflects a transition toward a cooler, more oxidized environment driven by the incursion and mixing of ambient seawater as the hydrothermal system waned. Trace element geochemistry of sphalerite reveals an average crystallization temperature of 265.8 °C (derived from the “GGIMFis” geothermometer), consistent with fluid inclusion data and representing a thermal “snapshot” of the waning hydrothermal stage. Systematic discriminant analysis using Ga/In, Ge/In, and Co-Ni-As systematics further confirms a strong magmatic–hydrothermal affiliation. Full article

The Somyne lake-mire system is a unique wetland landscape complex in the Polissia region of Ukraine and forms part of the Rivne Nature Reserve. Its ecological importance is internationally recognised through its designation as the Ramsar wetland “Somyne Peatland Massif”. Effective conservation of this wetland requires an understanding of the factors controlling the functioning of the lake and its drainage basin, considered in this study as a lake-basin system (LBS). The aim of this study is to assess the geoecological condition of the Somyne LBS using the principles of landscape limnology and the basin approach. The research integrates morphological, morphometric, hydrological, landscape-metric, hydrochemical and geochemical analyses. These are complemented by bathymetric modelling, landscape mapping, and analysis of long-term meteorological observations. The results identify key natural and anthropogenic drivers shaping the functioning of the system, characterise the hydrochemical state of lake waters and the geochemical properties of bottom sediments, and describe the spatial distribution of bottom sediments and the bathymetric structure of the lake basin. A multivariate algorithm for the geoecological assessment of lake-basin systems is proposed, providing a framework for comparative analysis of small lakes in the Polissian lake region under climate change and increasing anthropogenic pressure. Full article

Sub-sag 21 in the eastern Yangjiang Sag, Pearl River Mouth Basin, South China, contains a thick lacustrine source-rock interval within the lower Wenchang Formation and is a major exploration target on the northern margin of the South China Sea. However, the timing of deposition during the early to middle Eocene remains poorly constrained, and the applicability of quantitative palaeoclimate reconstruction methods in low-latitude lacustrine basins requires further evaluation. In this study, we analyzed mudstones from the lower Wenchang Formation in Well E1. Using cyclostratigraphic constraints, we applied AstroGeoFit to construct an astronomically tuned age model, and combined palynological coexistence analysis with geochemical weathering proxies and linear–regression calibration to quantitatively reconstruct and cross-validate mean annual temperature and mean annual precipitation. Within this time-calibrated framework, we further quantified organic-carbon burial to evaluate the relationship between palaeoclimate evolution and organic-matter enrichment. The AstroGeoFit results indicate that the top of the lower Wenchang Formation in Well E1 is constrained to 44.563 Ma, and that the studied succession spans 50.249–44.563 Ma. Palynological coexistence analysis identifies three palaeoclimate phases within this interval. Method evaluation shows that the temperature reconstruction based on major-element geochemistry agrees well with the pollen-based temperature record, whereas one precipitation reconstruction based on weathering proxies shows the most robust agreement and stability relative to the pollen-based precipitation record. Reconstructed mean annual temperature ranges from 10.77 to 22.20 °C, and reconstructed mean annual precipitation ranges from 1188.27 to 1871.89 mm. Correlation analyses on the tuned timescale show that precipitation is more strongly associated than temperature with organic-matter accumulation parameters, including total organic carbon and organic carbon accumulation rate, indicating that organic carbon burial in the eastern Yangjiang Sag lake basin was mainly controlled by hydrological forcing. During the Early Eocene Climatic Optimum, carbon burial in low-latitude lakes was, therefore, not a simple response to elevated temperature, but instead reflected the integrated effects of precipitation, runoff, stratification, material supply, transport, and preservation. The evolutionary sequence further suggests that early high productivity was diluted by rapid sedimentation, reducing total organic carbon; subsequent cooling, lake deepening, and strengthened stratification enhanced organic matter preservation; and finally, tectonic subsidence together with regional humidification promoted the development and long-term preservation of high-quality lacustrine source rocks. Full article

The Late Jurassic–Early Cretaceous Oloy complex was formed in the setting of convergence between the Chukotka microcontinent and the Kolyma–Omolon margin. Its evolution reflects the closure of the South Anyui Ocean, with controversial timing estimates. This study emphasizes the integration of lithological data with magmatic and metallogenic information to reconstruct geodynamic processes. The article presents the results of detailed petrographic and geochemical studies, Sm-Nd isotope analyses, and U-Pb dating of detrital zircons from Kimmeridgian–Lower Hauterivian volcaniclastic and epiclastic sandstones. Petrographic studies and U-Pb dating of detrital zircons identified the main sources at different stages and the amount of synchronous pyroclastic material. Isotope-geochemical investigations suggest a young undifferentiated arc provenance for Kimmeridgian deposits, whereas Tithonian–Valanginian sediments accumulated due to the erosion of more differentiated igneous rocks and input of clastic material from the continent. New data on changes in sedimentation environments and provenance enabled the tracing of the evolution of the Oloy arc. In the Kimmeridgian, the Oloy island arc existed on a heterogeneous basement, with south-dipping subduction towards the Kolyma–Omolon margin. During the Late Tithonian, the arc accreted and magmatic activity continued in the active margin setting. Collision initiated in the latter half of the Berriasian, reaching its active phase in the Valanginian time. Full article

Rivers contaminated with metals and petroleum hydrocarbons, such as polycyclic aromatic hydrocarbons (PAHs), are still a problem that threatens aquatic ecosystem function. This study describes iron- and sulfate-reducing bacteria, principal drivers of anaerobic organic matter decomposition in aquatic sediments. A polyphasic approach, including culture-dependent, i.e., enumeration by Most Probable Number (MPN), and independent, Sanger and Next Generation Sequencing (NGS) techniques, as well as analytical geochemical analyses, was employed. This study found exceptionally high levels of metals (Al, Mn, Zn, and Pb), PAHs, and sulfates compared to typical freshwater environments, likely due to co-contamination from past petroleum and steel production waste. Microbial communities were dominated by the Thermoproteobacteria. Analysis of the iron-reducing community determined that Geobacter, critical for degrading organic matter using iron, manganese, or arsenic, was the most prevalent genus. Additionally, the presence of diverse groups involved in sulfur cycling, represented by dsrAB genes, high numbers of viable sulfate reducers, a higher abundance of Geobacter, and high levels of sulfate and iron suggests that the cryptic sulfur cycle (CSC) may be operational in this system. In addition, sulfate and iron reducers are known to enhance biodegradation of organic pollutants in the presence of metal oxides and sulfate, and thus warrant further investigation in this co-contaminated system. Full article

The hydrogeochemical characterization of shallow volcanic lakes at the Sete Cidades Volcano (São Miguel, Azores) provides new insights into the processes controlling water chemistry in low-depth lacustrine systems within active volcanic environments. Fourteen lakes (0.6–4 m deep) were sampled during two campaigns (winter 2024 and spring/summer 2025), combining in situ physicochemical measurements and major ion analyses along vertical profiles. The lakes are holomictic, cold (11.3–17.6 °C), slightly acidic (pH 5.66–5.95), and weakly mineralized (EC ~65–69 µS/cm), indicating dilute waters of predominantly meteoric origin. Hydrochemical facies are dominated by Na–Cl type, with strong correlations between chloride and conductivity (r = 0.857), supporting a major contribution from marine atmospheric deposition. To move beyond correlation-based interpretation, Gibbs diagrams and saturation indices (PHREEQC) were applied to constrain the dominant geochemical processes. Most samples plot within the precipitation dominance field, while all calculated saturation indices are negative (SI < 0), indicating undersaturation with respect to carbonate, evaporite, and silicate minerals. These results demonstrate that water chemistry is primarily controlled by atmospheric inputs, with only minor contributions from water–rock interaction and negligible influence of evaporation or mineral equilibrium processes. Seasonal increases in HCO₃⁻ and dissolved CO₂ at depth suggest enhanced organic matter decomposition during warmer periods, highlighting the role of biogeochemical processes in modulating carbon dynamics in shallow systems. The absence of a clear hydrothermal signature further distinguishes these lakes from deeper volcanic systems in the Azores. This study provides the first integrated hydrogeochemical framework for shallow volcanic lakes in the region, combining classical hydrochemistry with process-based tools. The results establish a quantitative baseline for assessing environmental change and improve the interpretation of external (atmospheric) versus internal (geochemical and biological) controls in volcanic lake systems. Full article

This study characterizes the hydrochemistry and geochemical signature of the Upper Cretaceous geothermal aquifer in the Zharkunak zone (Eastern Ili Depression, SE Kazakhstan) using certified analytical datasets from five deep wells (5539, 1-RT, 3-T, 1-TP, and 2-TP). The waters are hyperthermal (89–103 °C), alkaline (pH 8.1–9.0), and weakly mineralized (TDS 0.3–1.0 g/L), with sodium-dominated facies ranging from Na–HCO₃–SO₄ to Na–SO₄–Cl. Hydrochemical analysis indicates that water–rock interaction and cation exchange are the primary controls on fluid evolution, with limited influence from evaporation or external salinity sources. Elevated fluoride (up to ~10 mg/L) and dissolved silica (H₂SiO₃, often >50 mg/L) reflect prolonged high-temperature interaction with silicate-rich lithologies under low Ca²⁺ conditions. Trace elements and radon activity (up to 0.32 nCi/L) further support deep, fault-controlled circulation pathways. PHREEQC modeling indicates near-equilibrium to slight supersaturation with respect to silica phases, suggesting a potential risk of silica scaling during cooling, while carbonate scaling remains limited. Although the dataset is based on discharge conditions from a limited number of wells, the results demonstrate that the Zharkunak system has strong geothermal utilization potential, with management considerations related to fluoride, radon, and silica scaling. Future work should focus on integrating isotopic analyses and reactive transport modeling to better constrain subsurface processes and long-term system behavior. Full article

The Yechangping super-large porphyry–skarn deposit is a key component of the East Qinling molybdenum metallogenic belt, central China. Magnetite is widely developed across all mineralization stages of this deposit, yet its systematic geochemical evolution and prospecting significance remain poorly constrained. This study presents in situ major- and trace-element analyses of magnetite via electron probe microanalysis (EPMA), laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), and elemental mapping, to unravel the ore-forming hydrothermal evolution and establish reliable prospecting indicators. Four magnetite generations are identified based on petrography and paragenetic relationships: late skarn stage (Mt1), oxide stage (Mt2 and Mt3), and polymetallic sulfide stage (Mt4). Magnetite has total iron contents (TFeO, total Fe calculated as FeO) of 82.72–95.46 wt.% (values above the 93 wt.% stoichiometric limit of pure magnetite stem from minor oxidation), with dominant isovalent Fe³⁺ and Al³⁺ lattice substitution supported by a significant negative Fe–Al correlation. Systematic stage-dependent geochemical variations are observed: Mt1 has the highest Ti (mostly >1500 ppm), V and Cr, while Mt2–Mt4 show progressive Ti depletion (mostly <100 ppm), recording continuous cooling of the hydro-thermal system. V and Cr contents decrease markedly from Mt1 to Mt3, with secondary enrichment in Mt4; Mo concentrations peak in Mt2 (average 5.06 ppm), coupled with elevated chalcophile metalloid Te, As, Pb and Bi. Elemental mapping results show that K occurs as discrete hotspots, which may be mainly derived from feldspar microinclusions, rather than lattice substitution in magnetite. These geochemical fingerprints record a transition from high-temperature magmatic–hydrothermal fluids to late contact-metasomatic fluids, with evolving fluid–rock interaction and oxygen fugacity. Our results demonstrate that magnetite chemistry is a reliable tool for discriminating mineralization stages and vectoring prospecting targets in porphyry–skarn Mo–W systems. Full article

The hydrothermal-filling-type tremolite jade (nephrite) deposit in sanchakou, Qinghai Province is hosted in marine dolomite, and its ore-forming fluid sources and metallogenic mechanisms remain poorly constrained. Here, we conducted an integrated study involving field geological mapping, petrographic observations, and geochemical analyses (major and trace elements, REEs, Sr isotopes) to constrain material sources, fluid physicochemical features and mineralization processes of the deposit. Results show that the ore-forming fluids were derived from deep crust, with homogeneous initial ⁸⁷Sr/⁸⁶Sr ratios ranging from 0.70949 to 0.70959, distinctly higher than the host dolomite (~0.707683), indicating intensive water–rock interaction with Sr-radiogenic lithologies during fluid upwelling. The host dolomite provided the main Ca and Mg, while Si and partial Mg were sourced from deep Si-Mg rich hydrothermal fluids, with negligible contribution from coeval gabbro. The ore-forming fluids were rich in Si, Mg, large-ion lithophile elements and volatiles (e.g., F⁻), characterized by medium-high to medium-low temperature evolution and fluctuating oxidation states. Mineralization can be divided into four stages: deep fluid generation and migration, infiltration metasomatism and silicification, tremolite crystallization at peak oxidation, and open-space filling and jade precipitation. High-quality tremolite jade mainly formed via pulsed hydrothermal injection and direct crystallization in tectonic fractures. This study establishes a genetic model for hydrothermal-filling-type nephrite, enriching relevant metallogenic theories and supporting subsequent exploration. Full article

The Jiangnan Orogenic Belt is a world-renowned metallogenic region for Au-W-Sb mineralization, with the Wangu deposit being a representative one. Previous research has demonstrated that tungsten in this Au-W-Sb deposit is sourced from the hosting metasedimentary rocks, but the specific mineral that provides tungsten is still unclear. This study evaluates the tungsten source by conducting petrographic observations and geochemical and geochronological analyses on the rutile from the host slate the Wangu deposit. The results show that rutile from wall rocks of the Wangu deposit yields an age of 955 ± 13 Ma, which is older than both the ore-forming age of the deposit and the age of the host strata. Electron microprobe analyses (EMPA) and laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) elemental analyses show that detrital rutile is enriched in elements such as Fe, Cr, V, and W, as well as high-field-strength elements (HFSE) including Nb, Ta, Zr, and Hf. The total rare earth element (ΣREE) ranges from 3.37 ppm to 156.85 ppm. The samples are generally enriched in light rare earth elements (LREEs) and exhibit distinct negative Eu anomalies. These geochemical features and a geochronological age of 955 ± 13 Ma suggest that the rutile is of detrital origin and they are possibly derived from the Grenvillian rocks. It is concluded that the detrital rutile in the metasediments could be an important source for hydrothermal tungsten enrichment. Full article