Search Results (26)

On 23 January 2024, a M_S7.1 earthquake struck Wushi County, Xinjiang Uygur Autonomous Region, marking the largest seismic event in the Southern Tianshan (STS) region in the past century. This study investigates the relationship between hydrothermal fluid circulation and seismic activity by analyzing the chemical composition and origin of fluids in natural hot springs along the Maidan Fracture (MDF). Results reveal two distinct hydrochemical water types (Ca-HCO₃ and Ca-Mg-Cl). The δD and δ¹⁸O values indicating spring water are influenced by atmospheric precipitation input and altitude. Circulation depths (621–3492 m) and thermal reservoir temperatures (18–90 °C) were estimated. Notably, the high ³He/⁴He ratios (3.71 Ra) and mantle-derived ³He content reached 46.48%, confirming that complex gas–water–rock interactions occur at fracture intersections. Continuous monitoring at site S13 (144 km from the epicenter of the Wushi M_S7.1 earthquake) captured pre-and post-seismic hydrogeochemical fingerprints linked to the Wushi MS7.1 earthquake. Stress accumulation along the MDF induced permeability changes, perturbing hydrogeochemical equilibrium. At 42 days pre-Wushi M_S7.1 earthquake, δ¹³C DIC exceeded +2σ thresholds (−2.12‰), signaling deep fracture expansion and CO₂ release. By 38 days pre-Wushi M_S7.1 earthquake, Na⁺, SO₄²⁻, and δ¹⁸O surpassed 2σ levels, reflecting hydraulic connection between deep-seated and shallow fracture networks. Ion concentrations and isotope values showed dynamic shifts during the earthquake, which revealed episodic stress transfer along fault asperities. Post-Wushi M_S7.1 earthquake, fracture closure reduced deep fluid input, causing δ¹³C DIC to drop to −4.89‰, with ion concentrations returning to baseline within 34 days. Trace elements such as Be and Sr exhibited anomalies 12 days before the Wushi M_S7.1 earthquake, while elements like Li, B, and Rb showed anomalies 24 days after the Wushi M_S7.1 earthquake. Hydrochemical monitoring of hot springs captures such critical stress-induced signals, offering vital insights for earthquake forecasting in tectonically active regions. Full article

Heavy metals (HMs) from industrial pollution are bioaccumulated in plant tissues, but we lack information on their spatial variability in forest ecosystems. Picea abies L. needles, bark, and litter were collected at 17 sites along a 1000-m-wide altitudinal gradient in southern Romania to measure concentrations of mineral nutrients, non-toxic metals, and toxic metals. Isotopic ratios (^206/207Pb, ^87/86Sr) were used to infer contamination origins. We found significant differences in needle versus bark and litter elements’ concentrations, indicating that needles are sensitive biomarkers in tracking air pollution. We found high Fe, Mn, Zn, and Cu concentrations, which can be involved in the low Na, Mg, and P content in needles. The mole ratios indicate a negative relationship with As concentrations in needles. Several environmental health and ecological risk assessment indices document that Cd levels can represent a moderate risk for most sites. Our study shows that P. abies presented an elevated bioaccumulation potential for Fe, Zn, Cu, Ni, and Cr, respectively, and it only absorbed Na, Sr, Cd, and Li. The methodology and results presented herein may serve as a reference for future studies and provide a foundation to develop management strategies to mitigate heavy metal pollution in forest ecosystems. Full article

In 44 BC, Julius Caesar established Colonia Laus Iulia Corinthiensis, strategically reviving Corinth to dominate Isthmian trade routes and extend Rome’s commercial influence eastwards. At the centre of the colony lies Temple E, an enigmatic structure with an unidentified associated cult. This study investigates the architectural characteristics of Temple E, focusing on the use of marble as the primary building material. Petrographic analysis, elemental chemical profiling (Mn, Mg, Fe, Sr, Y, V, Cd, La, Ce, Yb, U), and isotopic measurements (δ¹⁸O ‰, δ¹³C ‰) are employed to analyse marble samples from the surrounding region, exploring sourcing and construction practices. Statistical comparisons with ancient quarry databases indicate a strong reliance on locally sourced Doliana marble, underscoring the economic significance of regional quarries and suggesting the existence of a local workshop dedicated to architectural production in Roman Corinth. By integrating geological and archaeometric approaches, this study highlights Corinth’s pivotal role in the regional marble trade and its broader economic importance during the Roman Imperial period. The findings emphasise the use of local resources, illustrating a flourishing marble-working industry and enhancing our understanding of the relationship between local materials and Roman architectural practices. Full article

Recent studies have shown that the geothermal systems in Tibet are rich in rare metal elements such as lithium (Li), boron (B), rubidium (Rb), and cesium (Cs). However, the understanding of the origin of Cs-rich geyserite formed by hot springs remains unclear. In this study, a detailed petrological, elemental geochemical, and strontium–neodymium (Sr–Nd) isotopic investigation on Cs-rich geyserite in the Chabu region revealed that opal was the main mineral component of Chabu geyserite; here, some samples were rich in terrigenous clastic material, and well-developed diatom fossils were also present. Chabu geyserite had high contents of SiO₂ (78.95%–94.72%) and Al₂O₃ (3.02%–8.14%) and low contents of Fe₂O₃ (0.21%–1.94%), TiO₂ (0.01%–0.20%), MnO (0.01%–0.15%); additionally, the Fe/Ti ratio, the Al/(Al + Fe) ratio, and the Al/(Al + Fe + Mn) ratio showed large variations. These results indicated different degrees of participation by the terrigenous materials, hydrothermal deposition, and biogenic processes. Chabu geyserite was depleted in transition metal elements (e.g., Sc, V, and Cr) and high field strength elements (e.g., Nb, Zr, and Hf), relatively enriched in large-ion lithophile elements (e.g., Li, Rb, Sr, and Ba), and strongly enriched in Cs, (by up to 100 times the Cs content in the upper crust); in addition, it had low V/Y (1.30–2.00) and U/Th ratios. Chabu geyserite exhibited a right-dipping rare earth element (REE) distribution pattern and had significant negative Eu anomalies (0.26–0.72) and no or weak positive Ce anomalies (0.97–1.36). These results further indicated the influence of terrigenous clastic materials and nonhydrothermal sedimentation factors. The Sr–Nd isotopic composition of Chabu geyserite was significantly different from that of the mantle, with relatively high ⁸⁷Sr/⁸⁶Sr ratios (0.7070–0.7076) and low ¹⁴³Nd/¹⁴⁴Nd ratios (0.512223–0.512314). These ratios were similar to those of the crust. Combined with previous studies, the results from this study indicated that Chabu geyserite was a Cs-rich geyserite and was formed in an intracontinental post-collisional orogenic environment, mainly from crustal material, with the participation of biological and hydrothermal processes. Full article

We used otolith chemistry to test and complement current hypotheses regarding habitat use and connectivity between Dissostichus mawsoni sub-populations in Area 48 of the Commission for the Conservation of Antarctic Marine Living Resources (CCAMLR). Sagittal otoliths from 45 fish sampled near the South Orkney Islands were analysed. Their elemental (Li, Na, Mg, Cr, Mn, Sr, Sn, and Ba relative to Ca) and isotopic (δ¹⁸O and δ¹³C) signatures were examined in both the nuclear and marginal regions, representing juvenile and adult stages. Potential nursery habitats were geo-located by comparing observed and expected δ¹⁸O values. Chemical differences between the nuclear and marginal regions indicated ontogenetic migrations to deeper offshore habitats, suggesting a distinct habitat shift between 11 and 13 years of life. The data supported the existence of two nursery origins contributing to the study area’s population. However, the exact locations of these origins remain unclear and did not provide direct support for the hypotheses currently under consideration by the CCAMLR. Therefore, further assessment of the connectivity between nursery and adult habitats, as well as spawning site fidelity, is necessary before ruling out alternative hypotheses. Full article

Lithium possesses exceptionally high economic and strategic significance. China’s lithium resources rank second globally, predominantly found in salt lake brine. Recently, clay-type lithium deposits have been discovered in the Mahai Salt Lake within the Qaidam Basin, featuring a broad distribution area, stable production layers, and thick strata. This paper investigates the mineral sources and mining circumstances of the clay deposits in the study area through the principal trace elements and Sr and Li isotopes of the clay rocks. The study reveals that the sedimentation of the clay deposits in the study area is mainly semi-brine–brackish water phase sedimentation, formed in a shallow water environment of weak oxidation. A terrigenous source characterizes the clay sediment. The tectonic setting of the study area shares common traits with a continental island arc-active continental margin, and the abundant lithium clay rocks mainly receive contributions of feldspar, amphibole, pyroxene, etc. The primary sediment source of the clay deposits mainly stems from igneous and quartz sediment source areas. The ⁸⁷Sr/⁸⁶Sr value indicates that the Sr source of the clay rocks in the study area is the shallow over-pressured brine and Yuka River water, mainly derived from the weathering dissolution of silicate rocks. The δ⁷Li value indicates that the lithium in the lithium-rich clay rocks mainly originates from the release of lithium from silicate minerals in the surrounding mountain ranges, carried by Yuka River water, and from the supply of lithium from the deep Ca-Cl type water body. The research findings establish a foundation for the future exploration and development of clay-type lithium deposits in salt lake regions. Full article

Oceanic intraplate volcanoes sometimes experience late-stage eruptive activity known as rejuvenated volcanism, and contrasting interpretations for its petrogenesis depend on the compositional characteristics. In the Juan Fernández Ridge (JFR), a volcanic chain approximately 800 km in length emplaced on the Nazca Plate, some subaerial occurrences of rejuvenated volcanism have been recognized on the Robinson Crusoe and Santa Clara Islands, both part of the same deeply eroded shield volcano complex. This study aims to understand the origin and magmatic evolution of rejuvenated volcanism on Santa Clara Island, emplaced after ~2.15 Ma of quiescence above the shield sequence, mainly via the analysis of unpublished geochemical and isotopic data. Field reconnaissance identified two nearly coeval rejuvenated sequences on Santa Clara Island: Bahía W (BW) and Morro Spartan (MS), both formed by basanitic and picro-basaltic lava flows with brecciated levels and local intercalations of sedimentary and pyroclastic deposits. In comparison to the chemical signature of the preceding shield-building stage (comprised mainly of basalts and picrites), the two rejuvenated sequences exhibit a notable enrichment in incompatible elements, but the Sr, Nd, and Pb isotopes are very similar to the FOZO mantle endmember, with an apparent additional contribution of HIMU and EM1 components. The geochemistry of lavas revealed the involvement of various processes, including contamination by ultramafic xenoliths, high-pressure fractional crystallization of olivine and clinopyroxene, and potential partial assimilation of oceanic lithospheric components. While the oceanic lithosphere has been considered as a potential source, the isotopic data from Santa Clara lies outside of the mixing curve between depleted mantle (DM, here represented by the North Chile Rise and the East Pacific Rise) and the previous shield stage, suggesting that a lithospheric mantle is not the primary source for the rejuvenated stage volcanism. Therefore, we favor an origin of the rejuvenated volcanism from the mantle plume forming the JFR, supported by similarities in isotopic signatures with the shield stage and high values of ²⁰⁸Pb/²⁰⁴Pb (only comparable to San Félix—San Ambrosio in the vicinity of JFR), implying the presence of a regional source with radiogenic ²⁰⁸Pb/²⁰⁴Pb isotope ratios. In addition, isotopic variations are subparallel to the mixing line between HIMU and EM1 components, whose participation in different proportions might explain the observed trends. In conclusion, we propose that the source of the rejuvenated volcanism on Santa Clara Island is a heterogeneous mantle plume, the same one that fed the shield stage. The rejuvenated volcanism is derived from a secondary melting zone away from the main axis of the plume. Full article

The Saima alkaline rock-hosted niobium–tantalum deposit (hereafter referred to as the Saima Deposit) is situated in the Liaodong Peninsula, which constitutes the eastern segment of the northern margin of the North China Craton. The rock types of the Saima Deposit include phonolite, nepheline syenite, and aegirine nepheline syenite, which hosts niobium–tantalum ore bodies. In this study, the primary niobium-bearing minerals identified include loparite, betafite, and fersmite. The Saima pluton is characterized as a potassium-rich, low-sodium, and peraluminous alkaline pluton. Trace element characteristics reveal that the metallization-associated syenite is enriched in large-ion lithophile elements (LILEs) such as K and Rb but is relatively depleted in high-field strength elements (HFSEs). As indicated by the rare earth element (REE) profile, the Saima pluton exhibits a high total REE content (∑REE), dominance of light REEs (LREEs), and scarcity of heavy REEs (HREEs). The Sr-Nd-Pd isotopic data suggest that aegirine nepheline syenite and nepheline syenite share consistent isotopic signatures, indicating a common origin. The Saima alkaline pluton displays elevated I_Sr values ranging from 0.70712 to 0.70832 coupled with low ε_Nd(t) values between −12.84 and −11.86 and two-stage model ages (t_DM2) from 1967 to 2047 Ma. These findings indicate that the metallogenic materials for the Saima Deposit derive from both an enriched mantle source and some crustal components. The lithium (Li) isotopic fractionation observed during the genesis of the Saima pluton could be attributed to the differential diffusion rates of ⁶Li and ⁷Li under non-equilibrium fluid–rock interactions. Full article

The Reshui area, located to the northeast of the Qinghai–Tibet Plateau, exhibits complex geological conditions, well-developed structures, and strong hydrothermal activities. The distribution of hot springs within this area is mainly controlled by faults. In this paper, five hot springs from the area were taken as the research object. We comprehensively studied the geochemical characteristics and genetic mechanism of the geothermal water by conducting a field investigation, hydrogeochemistry and environmental isotopic analysis (⁸⁷Sr/⁸⁶Sr, δ²H, δ¹⁸O, ³H). The surface temperature of the geothermal water ranges from 84 to 91 °C. The geothermal water in the area exhibits a pH value ranging between 8.26 and 8.45, with a total dissolved solids’ (TDS) concentration falling between 2924 and 3140 mg/L, indicating a weakly alkaline saline nature. It falls into the hydrochemical type CI-Na and contains a relatively high content of trace components such as Li, Sr, B, Br, etc., which are of certain developmental value. Ion ratio analysis and strontium isotope characteristics show that the dissolution of evaporite minerals and carbonate minerals serves as a hot spring for the main source of solutes. Hydrogen and oxygen stable isotope characteristics findings indicate that the geothermal water is primarily recharged via atmospheric precipitation. Moreover, the tritium isotopic data suggest that the geothermal water is a mixture of both recent water and ancient water. Moreover, the recharge elevation is estimated to be between 6151 and 6255 m. and the recharge area is located in the Kunlun Mountains around the study area. The mixing ratio of cold water, calculated using the silicon enthalpy equation, is approximately 65% to 70%. Based on the heat storage temperature calculated using the silicon enthalpy equation and the corrected quartz geothermal temperature scale, we infer that the heat storage temperature of geothermal water in the area ranges from 234.4 to 247.8 °C, with a circulation depth between 7385 and 7816 m. The research results are highly valuable in improving the research level concerning the genesis of high-temperature geothermal water in Reshui areas and provide essential theoretical support for the rational development and protection of geothermal resources in the area. Full article

The Xiongcun Cu–Au ore district is in the southern middle Gangdese Metallogenic Belt, Tibet, and formed during Neo-Tethyan oceanic subduction. The Xiongcun ore district mainly comprises two deposits, the No. I and No. II deposits, which were formed by two individual mineralization events according to deposit geology and Re–Os isotopic dating of molybdenite. The No. I deposit is similar to a reduced porphyry copper–gold deposit, given the widespread occurrence of primary and/or hydrothermal pyrrhotite and common CH₄-rich and rare N₂-rich fluid inclusions. The No. II deposit, similar to classic oxidized porphyry copper–gold deposits, contains highly oxidized minerals, including magnetite, anhydrite, and hematite. The halogen chemistry of the ore-forming fluid from the No. I and No. II deposits is still unclear. Biotite geochemistry with halogen contents was used to investigate the differences in ore-forming fluid between the No. I and No. II deposits. Hydrothermal biotite from the No. I deposit, usually intergrown with sphalerite, is Mg-rich and classified as phlogopite and Mg-biotite, and hydrothermal biotite from the No. II deposit is classified as Mg-biotite. Hydrothermal biotite from the No. I deposit has significantly higher SiO₂, MnO, MgO, F, Li, Sc, Zn, Rb, Tl, and Pb contents and lower Al₂O₃, FeO_tot, Cl, Ba, Cr, V, Co, Ni, Y, Sr, Zr, Th, and Cu contents than the biotite from the No. II deposit. Hydrothermal biotites from the No. I and No. II deposits yield temperatures ranging from 230 °C to 593 °C and 212 °C to 306 °C, respectively. The calculated oxygen fugacity and fugacity ratios indicate that the hydrothermal fluid of the No. I deposit has a higher F content, oxygen fugacity, and log(fHF/fHCl) value and a lower log(fH₂O/fHF) value than the hydrothermal fluid from the No. II deposit. The biotite geochemistry shows that the No. I and No. II deposits formed from different hydrothermal fluids. The hydrothermal fluid of the No. I deposit was mixed with meteoric waters containing organic matter, resulting in a decrease in oxygen fugacity and more efficient precipitation of gold. The No. I and No. II deposits were formed by a Cl-rich hydrothermal system conducive to transporting Cu and Au. The decreasing Cl, oxygen fugacity, and temperature may be the key factors in Cu and Au precipitation. Biotite geochemistry allows a more detailed evaluation of the halogen chemistry of hydrothermal fluids and their evolution within porphyry Cu systems. Full article

Natural and anthropogenic factors highly influence the concentration of major (Na, Mg, K, Ca) and trace (Sr, Ba, Mn, Li) elements, anions (HCO₃⁻, NO₃⁻, SO₄²⁻, Cl⁻), and Sr isotopic signatures. The current study identified the Sr isotopic signature in groundwaters from the Southern Carpathians and Apuseni Mountains karst areas of Romania and its relation to the water’s chemistry. The Sr concentration ranged between 16.5 and 658 µg/L, but in most groundwaters, it was below 200 µg/L. A considerable spatial variation and a low temporal variation, with a slightly lower Sr concentration in the winter than in spring, were observed. The strong positive correlation of the Sr with Ca, Mg, K, and Na indicated the common source of these elements. The main source of the Sr in groundwaters was the dissolution of carbonates, especially calcite, and dolomite to a lesser extent. The ⁸⁷Sr/⁸⁶Sr isotopic ratio ranged between 0.7038 and 0.7158. Generally, waters with a high Sr concentration and moderate ⁸⁷Sr/⁸⁶Sr ratios indicated carbonate dissolution, whereas samples with low Sr concentrations and high ⁸⁷Sr/⁸⁶Sr ratios suggested the dissolution of silicates. Full article

The isotopic content (δ¹³C, δ²H, δ¹⁸O) and concentrations of 30 elements (Li, Na, Mg, P, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Rb, Sr, Ag, Cd, Ba, Pb, La, Ce, Pr, Nd, Sm, Eu, Gd, and Tb) were determined in different wild and cultivated berries (raspberry, seaberry, blackberry, cranberry, and blueberry). Partial least squares discriminant analysis (PLS-DA) was applied in order to develop models for differentiating berries according to their botanical origin and growing system. δ¹³C, δ²H, δ¹⁸O, Li, Na, Mg, P, Ca, V, Mn, Co, Ni, Zn, As, Rb, Sr, Ba, and Eu were identified as significant elements for the differentiation of berry species, based on which an 85% PLS-DA model accuracy was obtained. Similarly, the PLS-DA model developed for the growing system differentiation correctly classified 94.4% of the cultivated berries and 77.2% of the wild ones, based on the main predictors: δ¹³C, δ¹⁸O, Li, Na, Ca, Cr, Mn, Ni, Rb, and Ba. The developed PLS-DA model for the discrimination of wild blueberries from cultivated ones showed excellent levels of sensitivity (100%), specificity (100%), and accuracy (100%). Full article

Bottled waters are among the most important products in the human diet. In Morocco, eleven bottled mineral waters were analyzed (physicochemical composition and water stable isotopes) to identify their geologic origins and hydrochemical characteristics. The study of the ionic ratios shows that the mechanisms of water–rock interaction, such as the dissolution of carbonate and silicate minerals, influence the chemistry of these mineral waters, which are controlled by lithology and tectonics, sometimes with the influence of deep flux through fractures. The water from the Oulmes plateau shows a Na-HCO₃ chemical facies in relationship with alkaline granite. Moreover, the carbonated waters (EM_G and EM_GL) are characterized by high concentrations of Si, Li, Rb, Sr, and Cs due to deep CO₂ flux origin. The waters of Saiss, Middle Atlas, and Rif are of the Ca-HCO₃ type linked mainly to carbonate formation. The stable isotope contents of water range from −7.74 to −5.35‰ for δ¹⁸O and −45.4 to −30.4‰ for δD. The recharge altitude of the aquifer was estimated to be between 250 and 1200 m, following a δ¹⁸O altitudinal gradient between 0.25 and 0.27‰ per 100 m. The industrial production process and the natural presence or artificial addition of CO₂ can also influence the isotopic composition of water. These results can be a relevant guide to decision makers for better exploitation and assessment of the water quality. Full article

The present study investigated the isotopic and elemental profile (by IRMS and ICP–MS) of edible egg parts (29 egg whites and 29 yolks) mainly collected from Romania. In order to differentiate the egg white and yolk coming from different hen rearing systems (backyard and barn), Partial Least Square-Discriminant Analysis (PLS-DA) models were developed. The models’ accuracies for the discrimination according to the hen growing system were 96% for egg white and 100% for egg yolk samples, respectively. Elements that proved to have the highest discrimination power for both egg white and yolk were the following: δ¹³C, Li, B, Mg, K, Ca, Mn, Fe, Co, Zn, Rb, Sr, Mo, Ba, La, Ce, and Pb. Nevertheless, the important compositional differentiation, in terms of essential mineral content, between the edible egg parts (egg white and egg yolk) were also pointed out. The estimated daily intake (EDI), the target hazard quotient (THQ) for Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Cd, Pb, and As, as well as the hazard index (HI) were used to assess non-carcinogenic human health risks from egg consumption. The obtained results showed no noticeable health risks related to egg consumption for humans from the point of view of the potentially toxic metals. Full article

The paleosedimentary environment and paleoclimate of the Neogene Guantao Formation in the Liaodong sub-uplift of Bohai Bay Basin in China, which is an important oil and gas exploration horizon, are not clear owing to the lack of quantitative analysis. The paleosedimentary environment and paleoclimate can be qualitatively or semi-quantitatively reconstructed by sedimentary geochemical indicators sensitive to the environment and climate. Based on the evaluation of whether the elements and isotopes can effectively record paleosedimentary environment and paleoclimate information or not, the paleoclimate (temperature and humidity), paleoenvironment (salinity, water depth, redox conditions), and evolution of the paleoenvironment and paleoclimate are studied by analyzing the trace elements, carbon and oxygen isotopes, strontium isotopes, whole-rock mineral compositions, and clay minerals of mudstones of the Guantao Formation in the Liaodong sub-uplift, Bohai Bay Basin. The study results show that (1) according to the trace element distribution patterns, high concentrations of continental elements (Ti, Zr, Th), clay minerals, and detrital content, the Guantao Formation is a product of proximal deposits, and the provenance mainly originates from the intermediate–acidic magmatic rocks near surrounding uplifts. (2) The paleoclimate during the sedimentation of the Guantao Formation was mainly semi-arid and semi-humid, as revealed by the Sr/Cu ratio. However, the high Rb/Sr and ⁸⁷Sr/⁸⁶Sr ratios demonstrate that the paleoclimate is relatively warm and humid. (3) The paleosedimentary temperature calculated by the Sr content and δ¹⁸O is roughly 30 °C, indicating that the Guantao Formation was deposited in a subtropical to tropical climate. (4) The Guantao Formation was deposited in continental freshwater according to the Li, Ni, and Sr content, Sr/Ba ratios, ⁸⁷Sr/⁸⁶Sr ratios, and salinity index Z. (5) The water depth of the paleoenvironment of the Guantao Formation is mainly in nearshore shallow water, reflected by the Mn/Ti ratio and calculated by the Co content, and the oxidizing condition of the paleoenvironment of the Guantao Formation, reflected by the U/Th, V/Cr, and Ni/Co ratios, is in a good coupling relationship with this environment. (6) As revealed by the variations in the geochemical data in the section, the temperature, humidity, and water depth of the Guantao Formation gradually increased from the early to late period, while the salinity gradually decreased, and the chemical weathering effect gradually increased. Full article