Search Results (353)

Neoproterozoic iron formations (NIFs), deposited during Cryogenian glaciation events, are critical for understanding early Earth oxidation events and the evolution of glacial–interglacial environments. Apatite, a common accessory mineral in iron formations, holds significant implications for sedimentary environments and diagenetic processes, but these aspects remain underexplored. This study focuses on the Hengyang NIF in the Nanhua Basin, South China. Using whole-rock geochemistry and major and trace element analysis of apatite, we investigate the environmental significance of apatite and associated diagenetic processes. Our results show that the Hengyang NIF are formed through the mixing of low-temperature hydrothermal fluids, seawater, and terrigenous detrital materials, with hydrothermal contributions increasing progressively from the bottom to the top of the iron formation layers. Whole-rock geochemical proxies indicate that the depositional water column evolved from relatively oxidizing to weakly oxidizing conditions. The study further demonstrates that the rare earth element patterns in apatite, characterized by middle rare earth element enrichment, are primarily controlled by porewater chemistry during diagenesis. In contrast, Ce anomalies and the V/Cr and V/(V + Ni) ratios in apatite, which are strongly influenced by fluid–rock interactions and magnetite recrystallization, no longer reliably reflect the primary depositional environment. The Th/U ratio in apatite, due to its geochemical stability, aligns with whole-rock trends and serves as a more reliable redox proxy. Based on these findings, we propose a three-stage depositional-diagenetic model: the early and late stages are characterized by high-energy, rapid sedimentation with minimal diagenetic modification, while the middle stage is dominated by low-energy, stagnant conditions with slow sedimentation rates, leading to prolonged diagenesis and significant decoupling of mineral geochemical signatures. This study emphasizes the need to distinguish between sedimentary and diagenetic signals when using mineral geochemical proxies to reconstruct paleoenvironments and provides new insights into the genesis of Neoproterozoic iron formations. Full article

Understanding the soil–plant transfer of both essential and non-essential elements is crucial for evaluating the crop nutritional quality, environmental interactions, and food safety. This study delivered a multiyear and multielement assessment under field conditions of the element uptake, translocation, and accumulation in raspberry (Rubus idaeus L.), based on data collected over two growing seasons (2024–2025) in two contrasting Romanian agroecosystems. Two commercial cultivars (Opal and Delniwa) were investigated under fertilized and unfertilized conditions. The concentrations of essential macroelements such as Ca, Mg, Na, and K, as well as trace elements (Li and Sr), were determined in soils and fruits using ICP-OES and AAS. The soil–fruit transfer was quantified through the transfer factor, assisted by a robust statistical framework which integrated spatial–temporal variability and non-parametric analysis. The results highlighted two contrasting accumulation regimes. The essential macroelements revealed a dynamic uptake pattern driven by the physiological demand, soil availability, and fertilization. K exhibited the highest transfer capacity, while Ca had a restricted translocation to the fruits, due to the intrinsic transport limitations. On the other hand, Li and Sr revealed a constrained accumulation, characterized by low concentrations, weak responsiveness to fertilization, and a strong dependence on the soil geochemical background and interannual dilution processes. The spatial variability between the cultivation sites and year-to-year changes in the dilution intensity was evidenced as the dominant driver of the transfer efficiency, while the varietal differences had a secondary but detectable role, mainly for the Ca–Sr discrimination. Overall, the results evidenced that the multielement accumulation in the raspberries was governed by the interplay between the soil geochemistry, physiological transport constraints, and environmental variability. Furthermore, the research provided a field-based, multiyear evidence supporting improved soil management, cultivar selection, as well as the strategies that may increase the fruit nutritional quality while minimizing the trace element risks. Full article

The Xinqiao Cu-S polymetallic deposit is located in the Tongling ore concentration area of the Middle-Lower Yangtze River metallogenic belt. The orebodies consist of skarn orebodies and stratiform sulfide orebodies, but the genetic link between them remains controversial. In this study, magnetite was used as a proxy to systematically constrain the hydrothermal evolution from the intrusion to the contact zone and further to the stratiform orebodies. A representative drill hole (E603) was logged, and samples were systematically collected from the Jitou pluton outward to the contact zone. Composite samples from the 8–28 m interval were crushed and prepared as resin mounts for integrated TIMA automated mineralogy, BSE textural observation, and in situ LA-ICP-MS trace element analysis. Five types of magnetite (Mt1 to Mt5) were systematically identified. Mt1 occurs as inclusions within feldspar in the quartz monzodiorite. It exhibits typical magmatic magnetite characteristics and contains grid-like ilmenite exsolution, indicating crystallization during the late magmatic stage. Mt2 is distributed in the interstices of magmatic minerals, commonly showing hematitization and replacement of ilmenite exsolution lamellae by titanite. Its trace element geochemistry displays magmatic–hydrothermal transitional features. Mt3–Mt5 in the skarn and stratiform orebodies are paragenetic with retrograde alteration minerals (e.g., epidote, chlorite, and actinolite) and sulfides, and are characterized by low Ti, Al, and V contents and high Mg, Mn, and Sn contents, indicating a hydrothermal origin. From Mt3 to Mt5, (Ti + V) and (Al + Mn) decrease, while Zn and Mn increase, accompanied by a decrease in the (Si + Al)/(Mg + Mn) ratio. This reflects a trend of decreasing fluid temperature and progressively enhanced wall-rock buffering. The Mg-in-magnetite geothermometer yields relatively consistent results for Mt1–Mt3, but anomalously high temperatures for Mt4–Mt5. This suggests that the elevated Mg activity in the fluid, caused by reaction with carbonate wall rocks, can significantly influence the calculated temperatures. Therefore, this geothermometer should be used cautiously for magnetite in the outer skarn zone and interpreted in combination with other temperature constraints. The textures, paragenetic mineral assemblages, and trace element characteristics of magnetite collectively reveal a continuous mineralization process linking the skarn and stratiform orebodies at Xinqiao, providing robust mineralogical and geochemical evidence for the contribution of Yanshanian magmatic–hydrothermal activity to the stratiform mineralization. Full article

Cadmium (Cd) contamination in agricultural soils, especially in regions with a naturally high geochemical background such as Southwest China, poses a serious threat to food safety and the health of terrestrial ecosystems. Although arbuscular mycorrhizal fungi (AMFs) are known to enhance plant tolerance to heavy metals, the specific mechanisms by which dominant AMF species in karst soils—such as Funneliformis mosseae (Fm) and Rhizophagus intraradices (Ri)—immobilize Cd are not yet fully understood. In this study, a pot experiment with pepper plants was conducted to investigate the effects of Fm and Ri inoculation on Cd geochemistry in both the rhizosphere and bulk soil. Key results showed that AMF inoculation, especially with Fm, significantly reduced total Cd (by up to 33.8%) and bioavailable Cd (by up to 36.3%) concentrations in the soil, with a more pronounced effect within the rhizosphere. Accordingly, Cd content in pepper shoots was reduced by up to 15.0%. Inoculation also increased soil pH, organic matter, available phosphorus, and glomalin-related soil protein (GRSP) content. Redundancy analysis identified soil pH and total extractable GRSP as primary factors negatively correlated with Cd bioavailability. The study concludes that AMFs, particularly Fm, represent a potent bioremediation strategy by effectively immobilizing Cd in contaminated soils through mechanisms linked to GRSP production and pH elevation, thereby reducing its phytoavailability and translocation to edible plant parts. Full article

This study investigates four rock–soil profiles developed from Proterozoic intermediate–acid rocks in the Maoniushan area of Xichang, Sichuan Province. Through systematic geochemical analysis of major and trace elements and X-ray diffraction analysis of clay minerals, we aim to clarify the dominant controlling factors and environmental response mechanisms of chemical weathering under similar lithological and soil-forming age conditions. The results indicate the following: (1) Major element geochemistry shows that the Chemical Index of Alteration (CIA) of all profiles ranges from 61 to 74, while Na/K ratios and A-CN-K diagrams collectively reveal that the profiles are in a transitional stage from weak weathering (Ca and Na depletion) to moderate weathering (K depletion), with the weathering intensity ranking in the order TP1711 > TP1709 > TP1714 ≈ TP2801. (2) Trace elements exhibit significant differences among profiles: Cu, Zn, and Pb are significantly leached relative to Al₂O₃ in the TP1711 profile, whereas most trace elements are enriched in the TP1714, TP1709, and TP2801 profiles. Variations in ∑LREE/∑HREE ratios further support differences in the weathering stages of the profiles. (3) The clay mineral assemblages are dominated by illite, chlorite, and vermiculite. The TP1714 profile lacks vermiculite and has the highest illite content (54–60%), reflecting a relatively cold and dry local microclimate. In contrast, the other profiles show widespread vermiculite development, accompanied by minor kaolinite, indicating moderate weathering intensity under warm and humid climatic conditions. This study confirms that under similar lithological and soil-forming age conditions, the microclimatic differentiation induced by altitude variation is the key external controlling factor leading to spatial differences in the chemical weathering intensity of granite–soil profiles in the Maoniushan area. Full article

Soil provides essential ecosystem services and is pivotal for achieving multiple United Nations (UN) Sustainable Development Goals amid growing population pressures and resource demands. In arid to semi-arid regions such as Maio Island (Cape Verde), nutrient-poor soils and unsustainable land-use practices increase agricultural vulnerability, while volcanic geochemistry introduces elements that are not human friendly, further challenging environmental quality and long-term sustainability. Assessing soil (physical–chemical–biological) condition is therefore crucial for informed environmental and land-use planning. Here, Maio’s topsoil was evaluated using protocols adapted from Santiago, the largest Cape Verdean island. Estimated Background Values (EBVs) indicated naturally elevated V, Cr, Ni, Co, and Cu concentrations, consistent with mafic volcanic terrains. Robust Principal Component Analysis (rPCA) revealed geochemical groupings linked to volcanic–sedimentary units, with the dominant component (PC1) defined by Co–V–Cu–Mn–Ni versus As–Cd. Environmental Risk Indices (ERIs) and Multi-Element ERIs (ME–ERIs) quantified elemental enrichment relative to international land-use standards (residential and agricultural) and subsequently to Maio’s EBVs. The highest exceedances were observed for Cr, Co, Ni, V, and Cu, whereas As, Cd, Hg, Pb, and Zn fell within thresholds. The EBV-based assessment identified fewer exceedances than stricter international guidelines, though a few multi-element “hotspots” persist, highlighting potential land-use constraints and the need for preventive management. Overall, the integrated EBV/ERI/ME–ERI framework establishes an environmental geochemical baseline for Maio and offers a screening tool applicable across the entire archipelago. Full article

Analyzing the hydrochemical characteristics and formation mechanism of metasilicic acid (H₂SiO₃) enrichment in the groundwater of Sanjiang Plain is conducive to guiding the rational development and utilization of mineral water resources in this region. Taking the groundwater in the typical black soil area of the northeastern Sanjiang Plain (from Qindeli Farm to Chuangye Farm) as an example, 104 groups of groundwater samples were collected to analyze enrichment and controlling factors of H₂SiO₃ by comprehensive methods such as hydrochemical analysis, rock geochemistry, water–rock interaction analysis, and ion ratio analysis. The results showed that the groundwater was generally in a reducing environment with low mineralization and weak acidity. The main cations were Ca²⁺ and Mg²⁺, and the main anion was HCO₃⁻. The hydrochemical types were mainly HCO₃–Ca and HCO₃–Ca·Mg, followed by HCO₃·Cl–Ca·Mg mixed type, and the H₂SiO₃ enrichment rate of groundwater reached 80.77%. The enrichment of H₂SiO₃ in the groundwater was related to the local geological structure and specific hydrogeochemical processes, and mainly controlled by the hydrolysis process of silicate rock minerals (such as albite, plagioclase, and olivine). The silicates and aluminosilicates contained in the basalt, diorite, and gneiss distributed in the area provided a rich material basis for the enrichment of H₂SiO₃. Its migration and distribution were simultaneously affected by leaching and cation exchange, while NO₃⁻ and SO₄²⁻ input from anthropogenic sources also participated in the rock weathering, specifically the enrichment process of H₂SiO₃ in the groundwater. From the perspective of mineralization conditions, Qinglongshan Farm and Qindeli Farm are potential areas for developing H₂SiO₃-rich mineral water. However, the main direction for the development and utilization of groundwater in this area should be to explore natural H₂SiO₃-rich groundwater with good comprehensive water quality. Full article

This study investigates the rare-earth element (REE) geochemistry of twenty-nine clastic rock samples from the Paleogene Liushagang Formation in the Weixi’nan Sag. The primary objectives were to quantitatively evaluate the depositional paleoenvironment, determine the provenance lithology, and constrain the tectonic setting of the source area. Results reveal distinct chondrite-normalized REE distribution patterns characterized by light REE (LREE) enrichment, relatively flat heavy REE (HREE) segments, and pronounced negative Eu anomalies. The cerium anomaly index (Ce_anom, normalized to the North American Shale Composite) ranges from −0.06 to 0.00, implying broadly suboxic to anoxic-reducing conditions in the water column during deposition. The chondrite-normalized (La/Yb)_N ratio, utilized as a proxy for relative depositional residence time, decreases stratigraphically from member 3 to member 1, reflecting a transition to shorter residence times and higher relative sedimentation rates. Laterally, (La/Yb)_N increases toward the basin center, accurately recording progressively lower sedimentation rates basinward. Provenance analysis indicates that the sediments were predominantly derived from felsic igneous rocks of the upper continental crust. Spatially, the northern steep-slope belt reflects a uniform source, whereas the southern gentle-slope belt and the Weixi’nan low-uplift periphery record multisource mixed inputs. Finally, tectonic discrimination reveals an “active continental margin” affinity. This geochemical signature represents the inherited tectonic environment of the Mesozoic parent rocks in the surrounding source uplifts, rather than the Cenozoic extensional rift setting of the Weixi’nan Sag itself. Full article

The North China Craton (NCC) hosts numerous world-class Au deposits and these Au deposits can be classified into the Au-only and Ag-Au polymetallics, respectively. The former is mostly located in the eastern NCC, such as in the giant Jiaodong Province, and the latter is mostly distributed along the northern and southern margins of the NCC. Compared with Au-only deposits, the ore genesis of the Ag-Au deposits remains controversial. This paper focuses on the Niujuan Ag-Au deposit in the Fengning ore cluster of the northern margin of the NCC. Detailed deposit geology investigation, texture analysis, and analyses of the in situ trace element and sulfur isotope compositions of pyrite, coupled with H-O isotope compositions of quartz from different stages, were conducted to elucidate the ore-forming processes and metal sources. The results showed that the formation of the Niujuan deposit can be divided into four stages, including a pre-ore siliceous breccia stage (stage 1), syn-ore quartz-pyrite stage (stage 2), syn-ore polymetallic sulfide stage (stage 3), and post-ore fluorite-calcite stage (stage 4). Among these, stage 3 represents the major Ag-Au mineralization stage. Pyrite is well developed within stage 2 and stage 3, representing the intensive sulfidation of the wall rock. Microscopic analytical techniques including gamma-enhanced reflected light and scanning electron microscopy backscattered electron (BSE) reveal that pyrite samples from stage 2 and stage 3 have distinct textures. Pyrite (Py1) from stage 2 is homogeneous but with numerous pores. In contrast, pyrite (Py2) from stage 3 has overgrowth textures, and be divided into three sub-stages from core to rim (Py2a, Py2b, and Py2c) with different BSE brightness levels. LA-ICP-MS trace elements analyses results show that these different stages of pyrite show different composition such as Au, As, Ag, Co, and Ni. Py1 has low Au and Ag concentrations ranging from <0.1 ppm to 0.02 ppm and <0.1 ppm to 21.8 ppm, respectively. Py2a has low Au and Ag concentrations ranging from <0.1 ppm to 0.4 ppm and 0.4 ppm to 118.4 ppm, respectively. Py2b is characterized by high As and low Au contents, with average values of 6670.8 ppm for As and 1.4 ppm for Au. Py2c shows relatively low Co and Ni concentrations ranging from 0.02 ppm to 255.2 ppm and <0.1 ppm to 9.9 ppm, respectively. The sulfur isotope composition of Py1 and Py2 is relatively consistent, ranging from 3.8‰ to 6.7‰. The H and O isotope compositions of quartz from stage 1, stage 2, and stage 3 have insignificant variations, ranging from −119.5‰ to −101.3‰ for δD and −6.8‰ to −3.7‰ for δ¹⁸O_fluid, respectively. The results show that sulfur and, possibly, Au and Ag were mainly derived from magmatic hydrothermal fluids, and a significant amount of meteoric water was involved. Combined with the published mineralizing ages (~140 Ma), this paper suggests that the Niujuan Ag-Au deposit formed during the Early Cretaceous under an extensional setting in response to the eastward retreating subduction of the Paleo-Pacific oceanic plate. Evidence from deposit geology and geochemistry reveals that the mixture of magmatic and meteoric water, together with intensive sulfidation, is the key factor controlling Au and Ag deposition. Full article

The Dengshang Mo deposit is a recently recognized porphyry-type system within the Yanliao Mo metallogenic belt of northern Hebei Province. However, its ore-hosting rhyolitic porphyry emplacement age and petrogenesis remain insufficiently understood. This study integrates petrography, zircon U–Pb geochronology, Lu–Hf isotope analysis, zircon trace element geochemistry, and whole-rock major- and trace element data to investigate the petrogenesis of the Dengshang rhyolitic porphyry and its genetic relationship with Mo mineralization. The ore-hosting porphyry is predominantly composed of quartz and plagioclase phenocrysts. LA-ICP-MS zircon U–Pb dating yields an emplacement age of 168.3 ± 1.2 Ma, indicating that the rhyolitic porphyry was emplaced during a Middle Jurassic magmatic episode. Petrological and geochemical characteristics classify the Dengshang rhyolitic porphyry as an I-type granite. Zircon ε_Hf(t) values range from −0.93 to −7.29, corresponding to two-stage model ages (T_DM²) of 1.27–1.67 Ga, which suggests derivation from partial melting of the Mesoproterozoic lower crust. Zircon trace elements display significant positive Ce anomalies (δCe = 10.14–332.85), and calculated oxygen fugacities (ΔFMQ = −0.65 to +2.77; median = +0.51) indicate moderately oxidized magmatic conditions conducive to Mo enrichment. These results collectively imply that the Dengshang rhyolitic porphyry was emplaced at ~168 Ma associated with paleo-Pacific plate subduction. This geodynamic setting triggered partial melting of Mesoproterozoic lower crust, producing oxidized magmas that experienced fractional crystallization prior to shallow emplacement. Our findings elucidate the petrogenesis of the Dengshang rhyolitic porphyry and its control on Mo mineralization, and contribute new insight for understanding porphyry Mo genesis within the complex tectonic evolution of the Yanliao Mo Belt. Full article

This study presents a multiproxy paleoecological reconstruction from Laguna El Cacahuate, located ~180 km inland in the floodplain of Tabasco, southeastern Mexico, where red mangrove (Rhizophora mangle L.) forms persistent forest stands under freshwater conditions. We analyzed a 180 cm sediment core using pollen analysis, X-ray fluorescence geochemistry, and radiocarbon dating to investigate the environmental drivers of inland mangrove expansion. The core spans the last ~5200 years, capturing major shifts in vegetation and hydroperiod change. During the mid-Holocene, herbaceous freshwater taxa (Poaceae, Cyperaceae) dominated the floodplain under variable hydroclimatic conditions and high clastic input. The appearance of Rhizophora mangle pollen around 750 cal yr BP marks a significant ecological transition coinciding with geochemical indicators of stabilized flooding and reduced sedimentation. This inland colonization aligns temporally with increased regional precipitation and possible hydrogeomorphic changes following the 13th-century Plinian eruption of El Chichón. Unlike coastal mangroves, the persistence of Rhizophora under freshwater conditions supports the interpretation of this species as a facultative halophyte and indicates high resilience to long-term hydrological shifts. These findings provide critical insight into the ecological plasticity of mangroves, the paleoenvironmental history of the lower Usumacinta–San Pedro Basin, and the importance of integrating long-term records for wetland conservation strategies under future climate scenarios. Full article

The geochemistry of karstic paddy soils significantly influences Cd bioavailability and its accumulation by rice. However, there is limited research on Cd translocation and accumulation in rice, grown in paddy soil with elevated CaO and Zn levels. Addressing this, a field-based study in Hanyuan County, Sichuan Province, China, examined the Cd distribution and translocation patterns across the soil–root–straw–grain continuum, aiming to elucidate how elevated CaO and Zn levels regulate Cd accumulation in grains. The geochemical characterization of the soil revealed elevated concentrations of cadmium (Cd), calcium oxide (CaO), and zinc (Zn), with mean values of 2.12 ± 2.93 mg/kg, 5.77 ± 5.80 wt.%, and 359 ± 472 mg/kg, respectively. The sequential extraction results (by Tessier) demonstrated that the distribution of Cd followed the general order: residual > Fe-Mn oxide-bound ≈ exchangeable ≈ carbonate-bound > organic matter-bound. The exchangeable Cd content ranged from 0.063 to 0.93 mg/kg, accounting for up to 21.4% of the total Cd on average. The correlation analysis, Bioconcentration Factor (BCF), and Transfer Factor (TF) of Cd in different rice tissues, and structural equation modeling (SEM) revealed that elevated CaO and Zn levels in soil exhibit synergistic effects in inhibiting Cd accumulation in grains. Specifically, the CaO in soil reduces the Cd bioavailability by the formation of carbonate-bound specie (CdF2), thereby inhibiting Cd uptake by roots. In rice tissues, Zn could limit Cd translocation, particularly from roots to straws. Consequently, the regional rice Cd exceedance rate (25.8%) was significantly lower than that reported for other similar karst soils in China (over 50%). Full article

The Xiaotunxiang deposit, a newly discovered large-scale fluorite resource (1.28 Mt ore reserves) in southwestern Guizhou Province, China, provides a critical case study for understanding fluorite mineralization in the region. To constrain its genesis, this study integrates detailed ore deposit geology with mineralogy, trace element geochemistry, and strontium isotope analysis of fluorite. The ore mineral assemblage is dominated by fluorite, quartz, and calcite, with minor amounts of barite and pyrite. Trace element data reveal significant enrichment in Ti, Cr, Mo, and Sb relative to the upper continental crust. Fluorite exhibits moderate total REE contents (26.8–138 ppm), slight heavy REE enrichment (ΣLREE/ΣHREE = 0.17–1.88), pronounced negative Ce anomalies (δCe = 0.59–0.72), and negligible Eu anomalies (δEu = 0.95–1.14). These geochemical signatures are closely comparable to those of nearby fluorite deposits (Qinglong, Gaoling, and Getang), indicating a shared source of ore-forming materials. Strontium isotope ratios (⁸⁷Sr/⁸⁶Sr = 0.707468–0.707682) are consistent with local carbonate wall rocks, confirming their role as the primary source of calcium. We conclude that the Xiaotunxiang deposit formed from a low-temperature hydrothermal system where fluorine and associated metals were likely sourced from the Emeishan basalts, while calcium was derived from the interaction of acidic fluids with carbonate host rocks. Precipitation was ultimately triggered by fluid–rock (water/rock) interaction, classifying Xiaotunxiang as a carbonate-hosted hydrothermal deposit. Full article

Determining the age and origin of the “Huoshan Sandstone” holds significant geological implications for the stratigraphic division and correlation of Precambrian sequences in the North China Craton, provenance analysis, reconstruction of tectonic–sedimentary patterns, and paleogeographic settings restoration. This paper investigates the petrology, zircon U-Pb dating, Hf isotopes analysis, and zircon microzonation geochemistry of the “Huoshan Sandstone”. The “Huoshan Sandstone” is grayish-white, light gray, light yellow, purplish-red quartzitic sandstone and quartz sandstone, with a quartz content ranging from 85.5% to 97.8%. The quartz grains exhibit relatively straight contact edges, characteristic of low-grade metamorphosed quartzite. The protolith of the “Huoshan Sandstone” is a medium-grained quartz sandstone with dominant grain sizes of 0.30~0.50 mm, exhibiting well-rounded to subrounded grains and highly developed siliceous cementation characterized by secondary overgrowth. The zircon Th/U ratio confirms that the zircons in the “Huoshan Sandston” are mainly magmatic zircons. Most zircons exhibit extreme HREE enrichment and left-sloping REE patterns, and show significant positive Ce anomalies (Ce/Ce* of 1.06~290.68) and negative Eu anomalies (Eu/Eu* of 0.065~0.61). The age range of zircon ²⁰⁷Pb/²⁰⁶Pb is 1770 ± 20~2732 ± 16 Ma, and there are two obvious peaks at 1800 and 2500 Ma in the U-Pb age frequency histogram, the age of the intersection point on the concordia line is 2521 ± 31 Ma, and the age of the intersection point on the lower part of the line is 1829 ± 22 Ma. These two ages correspond to the timing of Neoarchean TTG gneiss formation through oceanic crust partial melting in the central North China Craton, and the ~1.85 Ga Paleoproterozoic thermal metamorphic event recorded in the Zhongtiao Group of the same region, respectively. The maximum depositional age of the “Huoshan Sandstone”, constrained by the youngest detrital zircon U-Pb ages at 1770 ± 20 Ma, indicates that its sedimentation occurred after 1770 ± 20 Ma (Late Late Paleoproterozoic). Furthermore, as it underlies the red shales of the Cambrian Mantou Formation as a distinct tectonic layer, it must have formed prior to the deposition of the Cambrian Mantou Formation. In addition, in situ Lu-Hf isotopic analyses of these zircons yielded two-stage model ages, mainly between 2.5 and 2.8 Ga, suggesting the provenance to be the Precambrian basement of the Zhongtiao Mountain region in the central North China Craton. It is inferred that the Precambrian strata in the Zhongtiao Mountain area were involved in the process of subduction, collage, and collision of the two continental blocks of the eastern and western parts of the North China Craton, and further confirmation is provided that the final collision of the two continental blocks to form the central orogenic belt occurred in the late Palaeoproterozoic. Full article

The Cambrian Period represents a critical yet debated interval in the global transition from “Aragonite Seas” to “Calcite Seas”. This study reconstructs the physicochemical evolution of paleoseawater through microstructural analysis and trace element geochemistry of Cambrian oolitic rocks in the northern Sichuan Basin, South China. Our results demonstrate that micrite envelopes on ooid margins and early submarine cements (Stage 1) effectively least-altered signals, resisting diagenetic alteration. Consequently, the maximum values of trace element in these fabrics serve as reliable proxies for paleoseawater reconstruction. Ooids from the upper Canglangpu Formation to the Longwangmiao Formation (Lower Cambrian, Series 2) are characterized by concentric laminations with tangential ultrastructures, high Sr contents (up to 1536 ppm), and high seawater molar Mg/Ca ratios (hereafter mMg/Ca, up to 5.02). These features contrast sharply with the radial fabrics, low Sr contents (<400 ppm), and low seawater mMg/Ca ratios (<0.4) observed in the Xixiangchi Formation (Upper Cambrian, Furongian). Integrating regional data with global correlations, this study confirms that Aragonite Sea conditions persisted on the northern margin of the Yangtze Block until at least the late Early Cambrian (Stage 4). The Middle Cambrian (Miaolingian) represents a pivotal transitional interval, leading to a complete shift to a stable Calcite Sea by the Late Cambrian (Furongian). These findings provide crucial regional constraints for refining the Phanerozoic model of seawater chemical evolution. Full article