Search Results (535)

The Muji Fault Zone (MJF) in the northeastern Pamir Plateau hosts a well-developed non-volcanic geothermal system, characterized by widespread hot springs and mud volcanoes—where core processes of geothermal fluids, including atmospheric precipitation recharge, shallow crustal circulation, carbonate-driven water–rock interactions, and CO₂-rich fluid discharge, are tightly coupled with regional intense crustal deformation and frequent seismic activity. We collected and analyzed 22 geothermal water samples and 8 bubbling gas samples from the MJF periphery, finding that the geothermal waters are predominantly of the HCO₃-Ca·Mg hydrochemical type, with hydrogen (δD: −103.82‰ to −70.21‰) and oxygen (δ¹⁸O: −14.89‰ to −10.10‰) isotopes indicating atmospheric precipitation as the main recharge source. The Na-K-Mg ternary diagram classified the waters as immature, reflecting low-temperature water–rock interactions in the shallow crust (<3 km), while noble gas isotopes (³He/⁴He: 0.03–0.09 Ra, Ra = 1.43 × 10⁻⁶) and carbon isotopes (δ¹³C-CO₂) confirmed fluid origin from crustal carbonate dissolution; SiO₂ geothermometry estimated thermal reservoir temperatures at 67–155 °C. Long-term monitoring (May 2019–April 2024) of Tahman (THM) and Bulake (BLK) springs revealed significant pre-seismic anomalies: before the 2023 Tajikistan Ms7.2 and 2024 Wushi Ms7.1 earthquakes, Na⁺, Cl⁻, and SO₄²⁻ concentrations showed notable negative anomalies (exceeding 2σ of background values) with synchronous trends between the two springs. Integrating these findings, a “Fault-Spring-Mud Volcano-Earthquake” fluid response model was established, providing direct evidence of deep-shallow fluid coupling in mud volcano–geothermal fluid interactions. This study enhances understanding of the dynamic evolution of non-volcanic geothermal systems under tectonic stress and clarifies the mechanisms of hydrogeochemical variations in fault-controlled geothermal systems, offering a robust scientific basis for advancing research on tectonic–fluid interactions in active fault zones of the northeastern Pamir Plateau. Full article

Boreholes in the Teleghma region of northeastern Algeria discharge thermal water with temperatures between 40 and 49 °C and total dissolved solids (TDS) ranging from 570 to 940 mg/L. The stable isotope compositions range from –7.8‰ to –6.2‰ for δ¹⁸O and –52.6‰ to –43.3‰ for δ²H, indicating a meteoric origin. Based on these isotopic signatures, the water is classified as immature and undersaturated with respect to the equilibrium line on the Giggenbach Na–K–Mg ternary diagram. The water exhibits a sodium–chloride (Na–Cl) facies, closely associated with Triassic formations rich in evaporitic deposits. This association was confirmed by the IIGR method, which illustrates the chemical evolution of the hydrothermal fluid as it ascends from the karstic carbonate reservoir through conduits and traverses clay formations. Consequently, computed saturation indices and applied inverse modeling significantly contributed to understanding the interactions between the hydrothermal water and the traversed rock. At the local scale, halite dissolution is the primary mineral phase driving chemical changes. Regionally, however, the processes are dominated by gypsum dissolution and cation exchange reactions between calcium and sodium ions. These findings offer valuable insights into the geochemical processes that shape the Teleghma geothermal system, with implications for resource management and potential applications. Full article

Salt lakes on the Tibetan Plateau (TP) are vital repositories of China’s strategic mineral resources, including boron and lithium. The Budongquan Salt Lake (BDQSL) in eastern Hoh Xil Basin (HXB) represents a hypersaline system with combined geothermal recharge and intense evaporation, yet its hydrochemical characteristics and B-Li enrichment mechanisms remain poorly understood. Through systematic hydrochemical and isotopic analysis (δD, δ¹⁸O, d-excess) of 69 surface samples, 14 depth-stratified profiles, and 131 regional water samples, we reveal that: (1) BDQSL exhibits extremely saline Na-Cl brines (TDS: 192,700–220,700 mg/L) significantly enriched in B and Li (45–54 mg/L), with overall spatial homogeneity and complete vertical mixing; (2) B and Li demonstrate strong correlation (R² = 0.95), controlled by coupled hydrothermal input, water–rock interaction, and evaporative concentration, with hydrothermal delivery as the predominant source; (3) depleted isotopic signatures (δ¹⁸O = −1.4‰, d-excess = −5‰) confirm intense evaporation, while upstream cascade connectivity and climate warming drive lake expansion and brine dilution, indicating transition toward lower salinity; (4) a distinctive hydrothermal–evaporative composite mineralization model differentiates BDQSL from regional mono-evaporative systems. This study elucidates B-Li enrichment mechanisms in hydrothermally active plateau salt lakes, providing geochemical constraints for resource assessment and predictive frameworks for evaluating mineral evolution under climate change. Full article

The Apuseni-Banat-Timok-Srednogorie Metallogenic Belt is one of the most important polymetallic metallogenic belts in the western segment of the Tethys, where numerous porphyry-type, skarn-type, and epithermal deposits are developed. However, scholars have noted a lack of systematic chronological and geochemical studies of andesites within this belt. Furthermore, the metallodynamic mechanisms controlling mineralization—such as oceanic plate exhumation and plate tearing—remain controversial. To complement the available research, this study focuses on andesites from the Čukaru Peki area in Serbia and integrates zircon U-Pb dating, molybdenite Re-Os isotopic analysis, and whole-rock geochemical analysis. The results reveal that plagioclase andesitic breccia and fine-grained plagioclase amphibole andesite were emplaced during the Late Cretaceous. Consistently, the molybdenite isochron age (81.46 ± 0.60 Ma, MSWD = 1.30) constrains the mineralization event to the same period. Both rock types exhibit geochemical signatures typical of island arc volcanic rocks, characterized by high SiO₂ contents and low Al₂O₃, MgO, and TiO₂ contents, as well as pronounced fractionation between light and heavy rare earth elements (LREEs and HREEs). The magma source is the mantle wedge metasomatized by fluid-rich melts derived from the dehydration of the subducted oceanic crust. Additionally, the primary magma produced by partial melting of this metasomatized mantle wedge assimilated and was contaminated by continental crustal material predating the Vardar Ocean’s closure during its ascent. Our findings suggest that the regional andesites are products of the exhumation of the Vardar Ocean. This study aims to provide a theoretical foundation for mineral exploration in the Timok ore cluster and, simultaneously, support the identification of ore prospecting targets in andesite alteration zones. Full article

In recent decades, increasing anthropogenic pressure and climate change have made the protection and sustainable management of groundwater resources essential. In this context, the identification of aquifer recharge zones, especially those characterized by rapid groundwater flow and high vulnerability to surface pollution sources, becomes a priority for the protection of underground resources. In the Po Plain (northern Italy), based on the lithological, geometric, hydraulic, and hydrodynamic characteristics of the aquifers, the recharge areas are mainly located in the alluvial fans of the Alpine and Apennine foothills. Due to the high hydraulic conductivity of the aquifer, the shallow depth of the water table and the agricultural activities, groundwater resources are vulnerable to nitrate (NO₃⁻) contamination. Given this background, the present study introduces a novel methodological approach based on the geochemical signature of groundwater, indicated by the presence of bicarbonate (HCO₃⁻) and NO₃⁻ ions, aimed at identifying aquifer recharge areas. Specifically, by analyzing time series of NO₃⁻ and HCO₃⁻ concentrations for the period 2012–2023, and applying criteria of an HCO₃⁻/NO₃⁻ ratio < 10 and NO₃⁻ > 30 mg/L, it was possible to identify areas where aquifer recharge processes are clearly evident. These recharge processes are rapid, as confirmed by the hydraulic gradient, the high hydraulic conductivity of the aquifers, and further supported by the isotopic composition of groundwater, especially tritium concentrations. Furthermore, due to the hydrogeological characteristics of the surveyed region, which resemble those of alluvial basins in close proximity to mountain ranges, the methodology and findings of this study can be used as an unconventional and expedited method for similar research conducted globally, offering hope for the future of groundwater research. Full article

Gnetol (trans-2,3′,5′,6-tetrahydroxystilbene), a naturally occurring stilbene structurally related to resveratrol (trans-3,5,4′-trihydroxystilbene; RES), has been reported to possess multiple health-promoting activities. In order to support its potential nutraceutical application, a reliable chromatography–tandem mass spectrometry (LC–MS/MS) assay was developed and validated for the quantitative determination of gnetol in mouse plasma and tissue samples, using isotopically labeled RES-¹³C₆ serving as the internal standard (IS). Electrospray ionization (ESI) was performed in negative mode, with multiple reaction monitoring (MRM) transitions m/z 243.2 → 175.0 for gnetol and m/z 233.1 → 191.0 for the IS. Chromatographic separation was achieved on a reversed-phase HPLC column using a 5-min gradient delivery of acetonitrile and 2 mM ammonium acetate at 0.5 mL/min and 40 °C. The linear calibration curve covered the concentration range of 5.0–1500 ng/mL, and the method validation confirmed its selectivity, accuracy, precision, stability, and dilution integrity. The developed method was subsequently applied to a biodistribution study in mice after oral administration of gnetol at 400 µmol/kg (equivalent to 97.7 mg/kg). Gnetol was rapidly absorbed and extensively distributed in key pharmacologically relevant organs. Despite its poor aqueous solubility, oral uptake was not significantly hindered. Collectively, these findings demonstrate that gnetol exhibits favorable absorption and tissue distribution profiles, supporting its promise as a candidate for nutraceutical development. Full article

Skarn-type iron ore is economically significant, and numerous skarn ore deposits have been identified in the North China Craton. The newly discovered orbicular diorite in this region is distinguished from other analogous rocks due to the accumulation of large magnetite particles, which may shed new light on the genesis of this ore type. The magnetite in different parts of the orbicular structure exhibits distinct compositional differences. For example, magnetite at the edge has a small particle size (200 μm) and is associated with the minerals plagioclase and hornblende, indicating that it crystallized from normal diorite magma. By contrast, magnetite in the core has a relatively large particle size (>1000 μm), is associated with apatite and actinolite, and contains apatite inclusions as well as numerous pores. The size of magnetite in the mantle falls between that of the edge and the core. The syngenetic minerals of magnetite in the mantle include epidote and plagioclase. The magnetites in the cores of orbicules have a higher content of Ti, Al, Ni, Cr, Sc, Zn, Co, Ga, and Nb than those in the rim. The δ⁵⁶Fe value of the core magnetite (0.46‰–0.78‰) is much higher than that of the mantle and rim magnetite in orbicules. Moreover, the δ⁵⁶Fe value of magnetite increases as the V content of magnetite gradually decreases. This large iron isotope fractionation is likely driven by liquid immiscibility that forms iron-rich melts under high oxygen fugacity. The reaction between magma and carbonate xenoliths (Ca, Mg)CO₃ during magma migration generates abundant CO₂, which significantly increases the oxygen fugacity of the magmatic system. Under the action of CO₂ and other volatile components, liquid immiscibility occurs in the magma chamber, and Fe-rich oxide melts are formed by the melting of carbonate xenoliths. Iron oxides (Fe₃O₄/Fe₂O₃₎ will crystallize close to the liquidus due to high oxygen fugacity. These characteristics of magnetite in the Tanling orbicular diorite (Wuan, China) indicate that diorite magma reacts with carbonate xenoliths to form “Fe-rich melts”, and skarn iron deposits are probably formed by the reaction of intermediate-basic magma with carbonate rocks that generate such “Fe-rich melts”. A possible reaction is as follows: diorite magma + carbonate → (magnetite-actinolite-apatite) + garnet + epidote + feldspar + hornblende + CO₂↑. Full article

Compression of clayey sediments not only causes land subsidence but also results in geogenic high fluoride groundwater. The distribution characteristics and enrichment mechanisms of fluoride in alluvial−lacustrine facies clayey sediments in the land subsidence area of Cangzhou Plain, China, were investigated using sample collection, mineralogical research, and hydrogeochemical and isotopic analysis. The results show that F⁻ concentration of groundwater samples ranged from 0.31 to 5.54 mg/L in aquifers. The total fluoride content of clayey sediments ranged from 440 to 792 mg/kg and porewater F⁻ concentration ranged from 0.77 to 4.18 mg/L. Clay minerals containing fine particles, such as muscovite, facilitate the enrichment of fluoride in clayey sediments, resulting in higher total fluoride levels than those in sandy sediments. The clay porewater F⁻ predominantly originated from the dissolution of water-soluble F and the desorption of exchangeable F from sediments. The F⁻ concentration in porewater was further influenced by ionic interactions such as cation exchange. The stable sedimentary environment and intense compression promoted the dissolution of F–bearing minerals and the desorption of adsorbed F in deep clayey sediments. The similar composition feature of δ²H−δ¹⁸O in deep groundwater and clay porewater samples suggests a significant mixing effect. These findings highlight the joint effects of hydrogeochemical and mineralogical processes on F behavior in clayey sediments. Full article

Recent studies suggest that Pb-based ammunition could be an important route of Pb exposure for Indigenous Peoples in tropical rainforests. We analyzed blood lead levels (BLL) and isotopic signatures in 111 humans, 97 wild animals, 81 fish, and potential environmental Pb sources in an Indigenous community in the remote and well-preserved Peruvian Amazon with no history of industrial activity. Median BLL was 11.74 μg dL⁻¹, with BLL ≥ 5 µg dL⁻¹ in 95.8% children <12-yo and 94.5% adults. Pb concentrations in wild animals were 7.00 ± 22.40 mg kg⁻¹ DW in liver, 0.06 ± 0.09 mg kg⁻¹ DW in fish muscle tissues, 17.1 ± 10.8 mg kg⁻¹ in soils and 3.4–3.8 mg L⁻¹ in the main river, although 0.43-0.53 mg L⁻¹ were the Pb levels in decanted water used for drinking and cooking. The similarity of isotopic signatures (^207/206Pb and ^208/206Pb) shows that the main Pb sources for humans are river waters (97.6%) and Pb-based ammunition (78.7%). Fish and wildlife act as Pb transporters from water, and wildlife act as Pb transporter from ammunition. Evidence of high human BLL in a remote, non-industrialized Amazonian area demonstrates the urgency of designing regional policies that include health prevention measures, focused on drinking water filtration systems and the use of non-toxic, Pb-free ammunitions. Full article

The Permian Kupferschiefer shale, a key stratigraphic unit within the Zechstein sequence of the Fore-Sudetic Monocline, represents both a metal-rich lithofacies and a potential source rock for hydrocarbon generation. This study presents a comprehensive geochemical characterization of selected Kupferschiefer samples obtained from the Legnica–Głogów Copper District (LGOM) and exploratory boreholes. Analytical methods included Rock-Eval pyrolysis, Py-GC/FID, elemental analysis, TG-FTIR, biomarker profiling, and stable carbon isotope measurements. Results indicate that the shales contain significant amounts of Type II and mixed Type II/III kerogen, derived primarily from marine organic matter with minor terrestrial input. The organic matter maturity, expressed by T_max, places most samples within the oil window. Rock-Eval S2 values exceed 60 mg HC/g rock in some samples, confirming excellent generative potential. Py-GC/FID data further support high hydrocarbon yields, particularly in samples from the CG-4 borehole and LGOM mines. The thermal decomposition of kerogen reveals multiple degradation phases, with evolved gas analysis identifying sulfur-containing compounds and hydrocarbons indicative of sapropelic origin. Isotopic compositions of bitumen and kerogen suggest syngenetic relationships and marine depositional settings, with samples from a North Poland borehole showing isotopic enrichment consistent with post-depositional oxidation. Kinetic parameters calculated using the Kissinger–Akahira–Sunose method demonstrate variable activation energies (107–341 kJ/mol), correlating with differences in organic matter composition and mineral matrix. The observed variability in geochemical properties highlights both regional and facies-dependent influences on the shale’s generative capacity. The study concludes that the Kupferschiefer in southwestern and northern Poland exhibits substantial hydrocarbon generation potential. This potential has been previously underestimated due to the unit’s thinness, but localized zones with high TOC, favorable kerogen type, and low activation energy could be viable exploration targets for natural gas. Full article

The Niland Moving Mud Spring, located near the southeastern margin of the Salton Sea, represents a rare and evolving geotechnical hazard. Unlike the typically stationary mud pots of the Salton Trough, this spring is a CO₂-driven mud spring that has migrated southwestward since 2016, at times exceeding 3 m per month, posing threats to critical infrastructure including rail lines, highways, and pipelines. Emergency mitigation efforts initiated in 2018, including decompression wells, containment berms, and route realignments, have since slowed and recently almost halted its movement and growth. This study integrates hydrochemical, temperature, stable isotope, and tritium data to propose a refined conceptual model of the Moving Mud Spring’s origin and migration. Temperature data from the Moving Mud Spring (26.5 °C to 28.3 °C) and elevated but non-geothermal total dissolved solids (~18,000 mg/L) suggest a shallow, thermally buffered groundwater source influenced by interaction with saline lacustrine sediments. Stable water isotope data follow an evaporative trajectory consistent with imported Colorado River water, while tritium concentrations (~5 TU) confirm a modern recharge source. These findings rule out deep geothermal or residual floodwater origins from the great “1906 flood”, and instead implicate more recent irrigation seepage or canal leakage as the primary water source. A key external forcing may be the 4.1 m drop in Salton Sea water level between 2003 and 2025, which has modified regional groundwater hydraulic head gradients. This recession likely enhanced lateral groundwater flow from the Moving Mud Spring area, potentially facilitating the migration of upwelling geothermal gases and contributing to spring movement. No faults or structural features reportedly align with the spring’s trajectory, and most major fault systems trend perpendicular to its movement. The hydrologically driven model proposed in this paper, linked to Salton Sea water level decline and correlated with the direction, rate, and timing of the spring’s migration, offers a new empirical explanation for the observed movement of the Niland Moving Mud Spring. Full article

Bisphenol A (BPA) has been listed as a substance of very high concern (SVHC) due to its endocrine-disrupting properties according to REACH in 2017. European competent authorities have prepared a REACH restriction proposal to reduce BPA levels in the environment. The proposed limit for the concentration of free BPA and other bisphenols in articles is 10 mg kg⁻¹. If exceeded, migration testing can demonstrate that no more than 0.04 mg L⁻¹ is released from the product or material over its lifetime. German authorities are drafting a new restriction proposal after the original was temporarily withdrawn. The residual and migration limits mentioned above were key requirements from the previous restriction proposal. Numerous national and international standards exist for assessing how environmental factors affect the physical and chemical properties of products and materials—such as notch impact strength and tensile strength—but these standards do not cover the release of pollutants. A standardised procedure that covers all aspects of artificial weathering and monitors the subsequent release of pollutants is necessary, especially in the context of the regulation of these substances. An accelerated weathering procedure was established for non-protected samples. This material was not intended for outdoor applications. The testing procedure applied a typical weathering scenario that represents Central European climate conditions. The procedure was validated and applied to samples under distinct quality assurance aspects. Released BPA is quantified via an organic isotope dilution LC-MS/MS method. In parallel, identical samples were weathered outdoors on a weathering rack. Haze and yellowness index are measured to compare outdoor and weathering chamber results. Full article

Kimberlite has attracted considerable interest among geologists as the primary source of natural gem-quality diamonds. The term “transitional kimberlite” was previously introduced to categorize rocks that exhibit bulk geochemical and Sr–Nd isotopic characteristics intermediate between those of archetypal kimberlite (formerly Group-I) and orangeite (formerly Group-II). Nevertheless, the petrogenesis of transitional diamond-bearing kimberlites remains poorly understood due to limited research. The diamondiferous transitional Wafangdian kimberlite in the North China Craton (NCC) thus provides a valuable opportunity for a detailed case study. We investigated fresh hypabyssal transitional Wafangdian kimberlites using bulk-rock major and trace element geochemistry to constrain near-primary parental magma compositions and decipher their petrogenesis. Geochemical compositions identify samples affected by crustal contamination based on elevated SiO₂, Pb, heavy rare earth element (HREE) concentrations, and Sr isotopic ratios. Compositional variations among macrocrystic samples (MgO: 29.7–31.5 wt.%; SiO₂: 30.6–34.7 wt.%; CaO: 3.9–7.5 wt.%; Mg^# [atomic Mg/(Mg + Fe²⁺) × 100]: 85–88) result from substantial entrainment and partial assimilation of peridotite xenoliths (up to 35%). In contrast, variations within aphanitic samples (MgO: 24.0–29.7 wt.%; SiO₂: 27.7–30.9 wt.%; CaO: 6.0–11.8 wt.%; Mg^#: 81–85) are attributed to fractional crystallization of olivine and phlogopite (~1–32%). Based on these constraints, the near-primary parental magma composition for the Wafangdian kimberlite is estimated as ~29.7 wt.% SiO₂, ~29.7 wt.% MgO, and Mg^# 85. Trace element concentrations in the transitional Wafangdian kimberlites resemble those of archetypal kimberlites globally (e.g., Nb/U > 26, La/Nb < 1.4, Ba/Nb < 16, Th/Nb < 0.25), indicating a shared convective mantle source. However, the Wafangdian kimberlites exhibit distinct characteristics: ε_Nd(t) values ranging from −3.44 to −1.77, higher Al₂O₃ and K₂O contents, and lower Ce/Pb ratios (10–20) compared to archetypal kimberlites. These features suggest the mantle source region was profoundly influenced by deeply subducted oceanic material. Full article

The Sahel Transboundary Taoudéni Basin, covering about 20% of Burkina Faso, hosts vital aquifers critical for water security and development. Effective groundwater monitoring is essential for sustainable resource management. In the Kou sub-basin, groundwater quality assessment is increasingly important. This study integrates hydrochemistry, water stable isotopes (δ¹⁸O, δ²H), GIS, and multivariate statistics to understand subsurface geochemical processes. A total of 48 samples—43 groundwater and 5 surface water—were analyzed for 19 hydrochemical parameters and isotopes. In surface water, δ¹⁸O ranged from −5.96‰ to −5.09‰, and δ²H from −37.65‰ to −29.15‰. In groundwater, δ¹⁸O ranged from −5.93‰ to −4.39‰, and δ²H from −34.62‰ to −25.05‰. The spatial distribution of δ¹⁸O and δ²H was mapped using inverse distance weighted (IDW) interpolation in ArcGIS 10.8. A δ²H vs. δ¹⁸O plot showed groundwater values clustered near the Global Meteoric Water Line, indicating minimal evaporation during recharge. Groundwater chemistry was dominated by Ca²⁺ > Na⁺ > Mg²⁺ > K⁺ and HCO₃⁻ > NO₃⁻ > Cl⁻ > SO₄²⁻. Key hydrogeochemical processes include water–rock interaction (leaching, weathering, ion exchange) and anthropogenic pollution. Isotopic signatures reveal heterogeneous recharge sources and aquifer connectivity. These findings enhance the understanding of water sources and geochemical processes in the Kou basin, supporting informed groundwater resource management. Full article

Geothermal resources in arid inland basins are important for clean energy development, yet their circulation and geochemical mechanisms remain insufficiently understood. This study investigates the hydrochemical characteristics and formation mechanisms of geothermal water in the Zhangye–Minle Basin, an arid inland region in northwestern China. A total of nine geothermal water samples were analyzed using major ion chemistry, stable isotopes (δ²H, δ¹⁸O), tritium (³H), and radiocarbon (¹⁴C) to determine recharge sources, flow paths, and geochemical evolution. The waters were predominantly of the Cl–Na and Cl·SO₄–Na types, with total dissolved solids ranging from 3432.00 to 5810.00 mg/L. Isotopic data indicated that recharge originated from atmospheric precipitation and snowmelt in the Qilian Mountains, with recharge altitudes between 2497 and 5799 m. Tritium and ¹⁴C results suggested that most samples were recharged before 1953, with maximum ages exceeding 40,000 years. Gibbs diagrams and ion ratio plots demonstrated that water–rock interaction was the primary geochemical process, while cation exchange was weak. Na⁺ was mainly derived from halite, albite, and mirabilite, while SO₄²⁻ originated largely from gypsum. The calculated reservoir temperatures using cation geothermometers ranged from 57 °C to 148 °C. The deep circulation of geothermal water was closely related to NNW-trending fault zones that facilitated infiltration and heat accumulation. These findings provide new insights into the recharge sources, circulation patterns, and geochemical processes of geothermal systems in fault-controlled basins, offering a scientific basis for their sustainable exploration and development. Full article