Search Results (396)

With the rapid increase in global lithium demand, the exploration of newly discovered lithium in the bauxite of the Wenshan area in southeastern Yunnan has become increasingly important. However, the current research on clay-type lithium in the Wenshan area has primarily focused on local exploration, and large-scale predictive metallogenic studies remain limited. To address this, this study utilized multi-source remote sensing data from ZY1-02D and ASTER, combined with ALOS 12.5 m DEM and Sentinel-2 imagery, to carry out remote sensing mineral identification, structural interpretation, and prospectivity mapping for clay-type lithium in the Wenshan area. This study indicates that clay-type lithium in the Wenshan area is controlled by NW, EW, and NE linear structures and are mainly distributed in the region from north of the Wenshan–Malipo fault to south of the Guangnan–Funing fault. High-value areas of iron-rich silicates and iron–magnesium minerals revealed by ASTER data indicate lithium enrichment, while montmorillonite and cookeite identification by ZY1-02D have strong indicative significance for lithium. Field verification samples show the highest Li₂O content reaching 11,150 μg/g, with six samples meeting the comprehensive utilization criteria for lithium in bauxite (Li₂O ≥ 500 μg/g) and also showing an enrichment of rare earth elements (REEs) and gallium (Ga). By integrating stratigraphic, structural, mineral identification, geochemical characteristics, and field verification data, ten mineral exploration target areas were delineated. This study validates the effectiveness of remote sensing technology in the exploration of clay-type lithium and provides an applicable workflow for similar environments worldwide. Full article

The most important bauxite deposits in Türkiye are located in the Seydişehir (Konya) and Akseki (Antalya) regions, situated along the western Taurus Mountain, with a total reserve of approximately 44 million tons. Some of the bauxite deposits have been exploited for alumina since the 1970s. In this study, bauxite samples, collected from six different deposits were examined to determine their mineralogical and chemical composition, as well as their REE content, with the aim of identifying which bauxite types are enriched in REEs and assessing their economic potential. The samples included massive, oolitic, and brecciated bauxite types, which were analyzed using optical microscopy, X-ray diffraction (XRD), X-ray fluorescence (XRF) and inductive coupled plasma-mass spectrometry (ICP-MS), field emission scanning electron microscopy (FESEM-EDX), and electron probe micro-analysis (EPMA). Massive bauxites were found to be more homogeneous in both mineralogical and chemical composition, predominantly composed of diaspore, boehmite, and rare gibbsite. Hematite is the most abundant iron oxide mineral in all bauxites, while goethite, rutile, and anatase occur in smaller quantities. Quartz, feldspar, kaolinite, dolomite, and pyrite were specifically determined in brecciated bauxites. Average oxide contents were determined as 52.94% Al₂O₃, 18.21% Fe₂O₃, 7.04% TiO₂, and 2.69% SiO₂. Na₂O, K₂O, and MgO values are typically below 0.5%, while CaO averages 3.54%. The total REE content of the bauxites ranged from 161 to 4072 ppm, with an average of 723 ppm. Oolitic-massive bauxites exhibit the highest REE enrichment. Cerium (Ce) was the most abundant REE, ranging from 87 to 453 ppm (avg. 218 ppm), followed by lanthanum (La), which reached up to 2561 ppm in some of the massive bauxite samples. LREEs such as La, Ce, Pr, and Nd were notably enriched compared to HREEs. The lack of a positive correlation between REEs and major element oxides, as well as with their occurrences in distinct association with Al- and Fe-oxides-hydroxides based on FESEM-EDS and EPMA analyses, suggests that the REEs are present as discrete mineral phases. Furthermore, these findings indicate that the REEs are not incorporated into the crystal structures of other minerals through isomorphic substitution or adsorption. Full article

Between approximately 725 and 518 Ma, a suite of specialized felsic plutons and granitic stocks were emplaced across the Arabian Shield, many of which are now recognized as highly mineralized prospects enriched in rare earth elements (REEs), rare metals, and radioactive elements bearing mineralizations. The current investigation focused on the radiological and geochemical characterization of naturally occurring radionuclides, specifically ²³⁸U, ²²⁶Ra, ²³²Th, and ⁴⁰K, within three strategically selected granitic prospects, namely, J. Tawlah albite granite (TW), J. Hamra (HM), and J. Abu Al Dod alkali feldspar syenite and granites (AD). Concerning the radioactivity levels of the investigated granitic stocks, specifically the activity concentrations of ²³⁸U, ²²⁶Ra, ²³²Th, and ⁴⁰K, the measured average values demonstrate significant variability across the TW, HM, and AD stocks. The average ²³⁸U concentrations are 195 (SD = 38.7), 88.66 (SD = 25.6), and 214.3 (SD = 140.8) Bq/kg for TW, HM, and AD granitic stocks, respectively. Corresponding ²²⁶Ra levels are recorded at 172.4 (SD = 34.6), 75.62 (SD = 25.9), and 198.4 (SD = 139.5) Bq/kg. For ²³²Th, the concentrations are markedly elevated in TW at 5453.8 (SD = 2182.9) Bq/kg, compared to 77.16 (SD = 27.02) and 160.2 (SD = 103.8) Bq/kg in HM and AD granitic stocks, respectively. Meanwhile, ⁴⁰K levels are reported at 1670 (SD = 535.9), 2846.2 (SD = 249.9), and 3225 (SD = 222.3) Bq/kg for TW, HM, and AD granitic plutons, respectively. Notably, these values exceed the global average background levels, indicating an anomalous enrichment of the studied granitic occurrences. The mean radiological hazard indices for each granitic unit generally exceed global benchmarks, except for AEDE_out in the HM and AD stocks, which remain below international limits. The geochemical disparities observed are indicative of post-magmatic alteration processes, as substantiated by the interpretation of remote sensing datasets. In light of the significant radiological burden presented by these granitic stocks, it is essential to implement a rigorous precautionary framework for any future mining. These materials must be categorically excluded from uses that entail direct human exposure, especially in residential construction or infrastructure projects. Full article

The Qiubudong silver deposit on the western margin of the Fuping ore cluster in the central North China Craton is a representative breccia-type deposit characterized by relatively high-grade ores, thick mineralized zones, and extensive alteration, indicating considerable potential for economic resource development and further exploration. Previous studies on this deposit have not addressed its genetic mineralogical characteristics. This study focuses on pyrite and quartz to investigate their typomorphic features, such as crystal morphology, trace element composition, thermoelectric properties, and luminescence characteristics, and their implications for ore-forming processes. Pyrite crystals are predominantly cubic in early stages, while pentagonal dodecahedral and cubic–dodecahedral combinations peak during the main mineralization stage. The pyrite is sulfur-deficient and iron-rich, enriched in Au, and relatively high in Ag, Cu, Pb, and Bi contents during the main ore-forming stage. Rare earth element (REE) concentrations are low, with weak LREE-HREE fractionation and a strong negative Eu anomaly. The thermoelectric coefficient of pyrite ranges from −328.9 to +335.6 μV/°C, with a mean of +197.63 μV/°C; P-type conduction dominates, with an occurrence rate of 58%–100% and an average of 88.78%. A weak–low temperature and a strong–high temperature peak characterize quartz thermoluminescence during the main mineralization stage. Fluid inclusions in quartz include liquid-rich, vapor-rich, and two-phase types, with salinities ranging from 10.11% to 12.62% NaCl equiv. (average 11.16%) and densities from 0.91 to 0.95 g/cm³ (average 0.90 g/cm³). The ore-forming fluids are interpreted as F-rich, low-salinity, low-density hydrothermal fluids of volcanic origin at medium–low temperatures. The abundance of pentagonal dodecahedral pyrite, low Co/Ni ratios, high Cu contents, and complex quartz thermoluminescence signatures are key mineralogical indicators for deep prospecting. Combined with thermoelectric data and morphological analysis, the depth interval around 800 m between drill holes ZK3204 and ZK3201 has high mineralization potential. This study fills a research gap on the genetic mineralogy of the Qiubudong deposit and provides a scientific basis for deep exploration. Full article

The Tuztaşı low-sulfidation epithermal Au–Ag deposit (Biga Peninsula, Türkiye) records a multi-stage hydrothermal history that can be interpreted through the trace and rare-earth-element (REE) chemistry of quartz. High-precision LA-ICP-MS analyses of five representative quartz samples (23 ablation spots; 10 analytically robust) reveal two fluid stages. Early fluids were cold, dilute meteoric waters (δ¹⁸O₍H₂O₎ ≈ −6.8 to +0.7‰), whereas later fluids circulated deeper, interacted with felsic basement rocks, and evolved in composition. Mineralized quartz displays marked enrichment in As (raw mean = 2854 ± 6821 ppm; filtered mean = 70 ± 93 ppm; one spot 16,775 ppm), K (498 ± 179 ppm), and Sb (57.8 ± 113 ppm), coupled with low Ti/Al (<0.005) and elevated Ge/Si (0.14–0.65 µmol mol⁻¹). Chondrite-normalized REE patterns show pronounced but variable LREE enrichment ((La/Yb)_n ≤ 45.3; ΣLREE/ΣHREE up to 10.8) and strongly positive Eu anomalies (δEu ≤ 9.3) with slightly negative Ce anomalies (δCe ≈ 0.29); negligible Ce–Eu covariance (r² ≈ 0.05) indicates discrete redox pulses. These signatures indicate chemically evolved, reducing fluids conducive to Au–Ag deposition. By contrast, barren quartz is characterized by lower pathfinder-element contents, less fractionated REE profiles, higher Ti/Al, and weaker Eu anomalies. A composite exploration toolkit emerges: As > 700 ppm, As/Sb > 25, Ti/Al < 0.005, Ge/Si > 0.15 µmol mol⁻¹, and δEu ≫ 1 reliably identify ore-bearing zones when integrated with δ¹⁸O data and fluid-inclusion microthermometry from earlier studies on the same vein system. This study provides one of the first systematic applications of integrated trace-element and REE analysis of quartz to a Turkish low-sulfidation epithermal system, offering an applicable model for vectoring mineralization in analogous settings worldwide. Full article

The rocks of the Burpala alkaline intrusion contain a wide range of rare minerals that concentrate rare earth elements (REEs), Nb, Th, Li, and other incompatible elements. One of the examples of the occurrence of such mineralization is albite–aegirine rocks located at the contact zone between the intrusion and the host terrigenous–sedimentary rock. In albite–aegirine rocks, cubic crystals of “metaloparite”, partially or completely substituted by bastnäsite-(Ce) and polymorphic TiO₂ phases (anatase and rutile) mainly represent the rare metal minerals. In albite–aegirine rocks, trace element minerals are predominantly represented by cubic crystals of “metaloparite”, which are partially or completely replaced by bastnäsite-(Ce) and polymorphic TiO₂ phases such as anatase and rutile. Additionally, Th-bearing zircon (up to 17.7 wt% ThO₂) and a variety of unidentified minerals containing REEs, Th, and Nb were detected. The obtained data indicate that bastnäsite-(Ce) is the result of the recrystallization of “metaloparite” accompanied by the formation of Th-bearing zircon and Nb-bearing rutile (up to 9.9 wt% Nb₂O₅) and the separation of various undiagnosed, unidentified LREE phases. Our studies show that remobilization of LREEs, HFSEs, and local enrichment of rocks in these elements occurred due to the effects of residual fluid enriched in fluorine and carbon dioxide. Full article

Coal combustion residues are increasingly viewed as alternative sources of rare earth elements (REEs), but their heterogeneous composition and post-depositional alteration complicate resource evaluation. This study analyzes 50 coal ash (CA) samples collected from a weathered dumpsite near Almaty, Kazakhstan, originating from power generation using coal from the Ekibastuz Basin. A multi-method approach—comprising bulk chemical characterization, unsupervised clustering, X-ray diffraction (XRD), scanning electron microscopy (SEM), and supervised machine learning (ML)—was applied to identify consistent indicators of REE enrichment. While conventional regression models failed to predict individual REE concentrations accurately, ML algorithms consistently highlighted vanadium (V) as the most robust predictor of ΣREE across Random Forest, XGBoost, and LASSO. This suggests that V may act as a geochemical proxy for REE-bearing phases, potentially due to co-retention in amorphous or ferruginous matrices. Despite compositional similarity among many samples, XRD and SEM revealed marked variability in phase structure and crystallinity, underscoring the limitations of bulk oxide data alone. These findings demonstrate that REE behavior in ash cannot be predicted deterministically, but ML can be used to screen for informative compositional signals. The proposed workflow may support the preliminary classification and valorization of heterogeneous ash materials in secondary resource strategies. Full article

The Oligocene Dongying Formation beach-bar system, widely distributed in the HHK Depression of the Bohai Bay Basin, constitutes a key target for mid-deep hydrocarbon exploration, though its provenance remains controversial due to complex peripheral source terrains. To address this, we developed an integrated methodology combining LA-ICP-MS zircon U-Pb dating with whole-rock rare earth element (REE) analysis, facilitating provenance studies in areas with limited drilling and heavy mineral data. Analysis of 849 high-concordance zircons (concordance >90%) from 12 samples across 5 wells revealed that Geochemical homogeneity is evidenced by strongly consistent moving-average trendlines of detrital zircon U-Pb ages among the southern/northern provenances and the central uplift zone, complemented by uniform REE patterns characterized by HREE (Gd-Lu) enrichment and LREE depletion; geochemical disparities manifest as dual dominant age peaks (500–1000 Ma and 1800–3100 Ma) in the southern provenance and central uplift samples, contrasting with three distinct peaks (65–135 Ma, 500–1000 Ma, and 1800–3100 Ma) in the northern provenance; spatial quantification via multidimensional scaling (MDS) demonstrates closer affinity between the southern provenance and central uplift (d_ij = 4.472) than to the northern provenance (d_ij = 6.708). Collectively, these results confirm a dual (north–south) provenance system for the central uplift beach-bar deposits, with the southern provenance dominant and the northern acting as a subsidiary source. This work establishes a dual-provenance beach-bar model, providing a universal theoretical and technical framework for provenance analysis in hydrocarbon exploration within analogous settings. Full article

Türkiye hosts a wide variety of barite deposits that can be broadly classified into two major groups based on their tectonic settings: magmatism-associated and passive margin-hosted deposits. The magmatism-associated deposits include Kızılcaören (F + Ba + REE + Th, Beylikova–Eskişehir), Kirazören (Bulancak–Giresun), and Karacaören (Mesudiye–Ordu). The Kızılcaören deposit formed in relation to the emplacement of a late Oligocene carbonatitic sill, while the Kirazören and Karacaören deposits are associated with the Cretaceous Pontide magmatic arc. Passive margin-hosted deposits occur within various Paleozoic sedimentary lithologies—such as metasandstone, shale, schist, and limestone—and are found in the Taurides and the Arabian Platform. These deposits occur as either concordant or discordant veins. This barite belt extends from Şarkikaraağaç (Isparta), through Hüyük (Konya) and Alanya (Antalya), to Silifke (Mersin), Tordere (Adana), Önsen, Şekeroba (Kahramanmaraş), and Hasköy (Muş). The Paleozoic deposits represent the major barite resources of Türkiye, with an annual production of approximately 300,000 metric tons. Smaller deposits around Gazipaşa (Antalya) contain minor Pb-Zn sulfides. Mesozoic barite deposits are hosted in Triassic dolomites and are associated with Pb-Zn mineralization in the Hakkari region of the Arabian Platform. Pb and Sr isotope data indicate that the barium in these deposits was derived from ancient continental crust. The isotopic compositions of both concordant (stratabound) and discordant (vein-type) barites are generally homogeneous. In northwestern Türkiye, the Sr isotope compositions of the barite deposits align well with those of the Oligocene carbonatite host complex. The ⁸⁷Sr/⁸⁶Sr isotope ratio of the Kızılcaören deposit (0.706‰) is the least radiogenic among Turkish barite deposits, suggesting a mantle contribution. The Kirazören deposit in the Pontide magmatic arc follows with a slightly higher ratio (0.707‰). Triassic barites from the Hakkari region yield ⁸⁷Sr/⁸⁶Sr values around 0.709‰, slightly more radiogenic than coeval seawater. Paleozoic barite deposits show the most radiogenic ⁸⁷Sr/⁸⁶Sr values, including Aydıncık (0.718‰), Şarkikaraağaç (0.714‰), Hasköy (0.713‰), Kahramanmaraş (0.712‰), Tordere, and Hüyük (both 0.711‰), consistent with their respective host rocks. The elevated radiogenic Pb and Sr isotope values in the passive margin-hosted deposits suggest that the barium originated from deeper, barium-enriched rocks, whereas stable sulfur isotope data point to a marine sulfur source. Moreover, Sr and S isotopic signatures indicate that the Paleozoic sediment-hosted deposits formed in association with cold seeps on the seafloor, resembling modern analogs. In contrast, the Mesozoic Karakaya deposit (Hakkari) represents a typical vent-proximal, sediment-hosted deposit with no magmatic signature. Full article

Late Paleozoic to Early Mesozoic granitoids in the East Kunlun Orogenic Belt (EKOB) provide critical insights into the complex and debated relationship between Paleo–Tethyan magmatism and tectonics. This study presents integrated bulk-rock geochemical and zircon isotopic data for the Xingshugou monzogranite (MG) to address these controversies. LA-ICP-MS zircon U-Pb dating constrains the emplacement age of the MG to 247.1 ± 1.5 Ma. The MG exhibits a peraluminous and low Na₂O A₂-type granite affinity, characterized by high K₂O (4.69–6.80 wt.%) and Zr + Nb + Ce + Y (>350 ppm) concentrations, coupled with high Y/Nb (>1.2) and A/CNK ratios (1.54–2.46). It also displays low FeO^T, MnO, TiO₂, P₂O₅, and Mg^# values (26–49), alongside pronounced negative Eu anomalies (Eu/Eu* = 0.37–0.49) and moderately fractionated rare earth element (REE) patterns ((La/Yb)_N = 3.30–5.11). The MG exhibits enrichment in light rare earth elements (LREEs) and large ion lithophile elements (LILEs; such as Sr and Ba), and depletion in high field strength elements (HFSEs; such as Nb, Ta, and Ti), collectively indicating an arc magmatic affinity. Zircon saturation temperatures (T_Zr = 868–934 °C) and geochemical discriminators suggest that the MG was generated under high-temperature, low-pressure, relatively dry conditions. Combined with positive zircon ε_Hf(t) (1.8 to 4.7) values, it is suggested that the MG was derived from partial melting of juvenile crust. Synthesizing regional data, this study suggests that the Xingshugou MG was formed in an extensional tectonic setting triggered by slab rollback of the Paleo-Tethys Oceanic slab. Full article

A study was carried out with a representative data set of volcanic lakes from the Azores archipelago. A total of 672 samples were collected during four field surveys conducted over the year and along the depth. Following water sampling, temperature, pH, and EC were measured, the dissolved CO₂ and alkalinity were determined by titration, and aliquots were taken to perform analysis of major, minor and trace elements, as well as ¹⁸O/¹⁶O, ²H/¹H and ⁸⁷Sr/⁸⁶Sr isotopic ratios. Waters are of meteoric origin and from the Na-HCO₃ to Na-Cl types. The ⁸⁷Sr/⁸⁶Sr ranges between 0.709194 and 0.704294, and most of the lakes depict less radiogenic values than seawater, suggesting a potential contribution from rock dissolution. Along the reciprocal of the Sr vs. ⁸⁷Sr/⁸⁶Sr plot, most samples suggest a linear trend between rock values and rainwater. Samples display considerable variability in the ∑REE, ranging from 0.83 µg L⁻¹ to 13.54 µg L⁻¹, and when chondrite normalized, depict a negative slope, showing an enrichment in light REEs compared to heavy REEs. This pattern is consistent with the one from Azores rocks and bottom sediments from some lakes, and most lakes depict Eu anomalies, resulting from interaction between water and sediments or from incongruent mineral dissolution. Full article

The peralkaline granites of the Papanduva Pluton (South Brazil) display a remarkable facies dichotomy, with zircon dominant in massive facies and diverse zirconosilicates (Zr-Si) in foliated facies. This study employs petrography and mineral chemistry (major and trace elements) to elucidate the textural diversity and compositional evolution of these minerals. Three discrete zirconosilicate groups were identified: Na-rich elpidite (euhedral, vein-like, and granular varieties), Na-poor (Na,K)Zr-Si-I, and silica-rich (Na,K)Zr-Si-II. Contrary to the expected crystallization sequences, trace element data reveal that REE enrichment correlates with deformation intensity rather than paragenetic order, with vein-like aggregates along deformation features showing the highest REE concentrations. Statistical analysis demonstrates significant correlations between REE contents and alkali exchange patterns. We propose a three-stage evolutionary model involving magmatic crystallization, deformation-enhanced fluid interaction, and late-stage recrystallization, with a progressive evolution from Na-dominated to K-dominated conditions. This study provides new insights into closed-system fluid evolution in agpaitic environments and highlights deformation as a primary control on element mobility in peralkaline granitic systems. Full article

The composition of wolframite from ores of the Porokhovskoe and Yugo-Konevskoe W greisen deposits in the Central Urals is studied using SEM-EDS and LA-ICP-MS analyses. The Porokhovskoe deposit is localized in a metamorphosed volcanosedimentary sequence of Lower Silurian age, and the Yugo-Konevskoe is enclosed in an eponymous granite pluton of Middle Permian–Lower Triassic age. Most studied wolframite grains belong to hűbnerite. The Fe/(Fe + Mn) value of wolframite varies in a range of 0.02–0.50. Wolframite from both deposits is enriched in Zn, Nb, and Mg. The wolframite from the Porokhovskoe deposit is enriched in V, Sc, Zn, and Mg and is depleted in Mo, U, rare earth elements (REEs), Nb, and Ta, compared to wolframite from the Yugo-Konevskoe deposit. It is suggested that this difference is due to the occurrence of ore veins in different rocks at different distance from the source of the ore-forming fluid, which cools down as it moves away from the source, leading to a decrease in the incorporation of trace elements by the lower-temperature wolframite. The predominance of heavy REEs over light REEs in all the studied wolframite is explained by the close ionic radii of heavy REEs to the main mineral-forming elements Fe and Mn. Full article

Rare earth elements (REEs) are critical mineral resources that play a pivotal role in modern technology and industry. Currently, the global supply of light rare earth elements (LREEs) remains adequate. However, the supply of heavy rare earth elements (HREEs) is associated with substantial risks due to their limited availability. Ion-adsorption type rare earth deposits (IAREDs), which represent the predominant source of HREEs, have become a focal point for exploration activities, with a notable increase in global interest in recent years. This study systematically collected stream sediments and stream water samples from the Jiaping IARED in Guangxi, as well as from adjacent granitic and carbonate background areas, to investigate the exploration significance of geochemical surveys for IAREDs. Additionally, mineralized soil layers, non-mineralized soil layers, and bedrock samples from the weathering crust of the Jiaping deposit were analyzed. The results indicate that stream sediments originating from the Jiaping IARED and granite-hosted background regions display substantially elevated REE concentrations relative to those from carbonate-hosted background areas. Moreover, δEu values in stream sediments can serve as an effective indicator for differentiating weathering products derived from granitic and carbonate lithologies. Within the mining area, three coarse-grained fractions of stream sediments (i.e., +20 mesh, 20–60 mesh, and 60–150 mesh) exhibit REE concentrations comparable to those observed in both granite-hosted and carbonate-hosted background regions. However, the HREEs content in the finer -150-mesh stream sediments from Jiaping IARED is markedly higher than that in the two background regions. The (La/Sm)_N versus (La/Yb)_N ratios of -150-mesh stream sediments in the Jiaping IARED may reflect the mixing processes involving HREE-enriched ore layer, non-mineralized layer, and LREE-enriched ore layer. This observation implies that fine-grained (-150-mesh) stream sediments can partially inherit the REE characteristics of mineralized layers within IAREDs. Scanning electron microscopy (SEM) observations indicate that the enrichment of REEs in fine-grained stream sediments primarily originates from REE-rich accessory minerals derived from parent rocks and mineralized weathering crusts. A comparative analysis reveals that the concentrations of REEs in stream water collected during the rainy season are significantly higher than those collected during the dry season. Moreover, the levels of REEs, especially HREE, in stream water from the Jiaping IARED substantially exceed those in background areas. Collectively, these findings suggest that the geochemical signatures of REEs in rainy season stream water possess diagnostic potential for identifying IAREDs. In conclusion, the integrated application of geochemical surveys of stream water and -150-mesh stream sediments can effectively delineate exploration targets for IAREDs. Full article

The Minghuazhen Formation in the Cangdong Sag of the Bohai Bay Basin is a key sedimentary unit for investigating regional provenance evolution, paleoclimate variations, and hydrocarbon potential in Eastern China. This study integrates mineralogical and geochemical analyses to explore sedimentary characteristics. Techniques include X-ray diffraction (XRD), major/trace element compositions, rare earth element (REE) distributions, and organic carbon content. XRD data and elemental ratios (e.g., Al/Ti, Zr/Sc) suggest a predominant felsic provenance, sourced from acidic magmatic rocks. The enrichment with light rare earth elements (LREE: La–Eu) and notable negative Eu anomalies in the REE patterns support the interpretation of a provenance from the Taihangshan and Yanshan Orogenic Belts. Geochemical proxies, such as the Chemical Index of Alteration (CIA) and trace element ratios (e.g., U/Th, V/Cr, Ni/Co), indicate a warm and humid depositional environment, characterized by predominantly oxic freshwater conditions. Organic geochemical parameters, including total organic carbon (TOC), total nitrogen (TN), and C/N ratios, suggest that organic matter primarily originates from aquatic algae and plankton, with C/N values predominantly below 10 and a strong correlation between TOC and TN. The weak correlation between TOC and total carbon (TC) indicates that the organic carbon is mainly biological in origin rather than carbonate-derived. Although the warm and humid climate promoted the production of organic matter, the prevailing oxic conditions hindered its preservation, resulting in a relatively low hydrocarbon generation potential within the Minghuazhen Formation of the Cangdong Sag. These findings provide new insights into the sedimentary evolution and hydrocarbon potential of the Bohai Bay Basin. Full article