Search Results (59)

Two-dimensional electron gases (2DEGs) at complex oxide interfaces have emerged as a promising platform for next-generation oxide semiconductor devices, owing to their tunable electronic properties and rich interfacial phenomena. In this work, a LaAlO₃/SrTiO₃/LaTiO₃ (LAO/STO/LTO) trilayer heterostructure is proposed and theoretically investigated using a self-consistent Schrödinger–Poisson framework to examine the effects of multi-interface engineering on quantum confinement and carrier transport. The proposed architecture combines polar-discontinuity-driven electronic reconstruction at the LAO/STO interface with charge-transfer-induced electron accumulation at the STO/LTO interface, forming two coupled 2DEG channels within the SrTiO₃ layer. Compared with conventional single-interface oxide heterostructures, the coupled-interface configuration significantly enhances sheet carrier density and electrical conductivity, with predicted carrier densities approaching 10¹⁴ cm⁻² and gate-tunable conductivities in the range of 10³–10⁴ S cm⁻¹ under idealized operating conditions. The effects of layer thickness, gate bias, temperature, and electrostatic coupling are systematically investigated to establish practical design guidelines for optimizing carrier confinement and transport. A sensitivity analysis incorporating interface trap densities up to 2 × 10¹³ cm⁻² demonstrates that more than 60% of the ideal carrier population is retained under moderate defect concentrations, confirming the robustness of the proposed multi-interface strategy. Although the analytical model represents an upper-bound framework, its predictions are discussed in the context of experimentally relevant limitations, including interface roughness, oxygen vacancies, carrier trapping, and defect-induced scattering. Overall, the proposed LAO/STO/LTO heterostructure provides a predictive framework for engineering high-density, electrically tunable oxide 2DEGs for future nanoelectronic, terahertz, photonic, and energy-related applications. Full article

Rock-forming minerals, olivine and pyroxene, from three ore-bearing intrusions in the Norilsk districts were studied. They are the Norilsk 1 and the Northern and Southern Maslovsky massifs with PGE-Cu-Ni ores, located in the Norilsk syncline. Trace elements such as Al, Ti, Co, Cu, Nd, Sm, Ce, Cr, V, Dy, Y, Yb, Er, Sr, and Eu were determined by LA-ICP-MS. The authors found differences in mineral compositions between picritic gabbro-dolerites from these intrusions. The parental melt of the Southern Maslovsky intrusion corresponded to tholeiitic basalt containing (wt.%) H₂O—0.65, CO₂—0.16, and B—0.004. It was concluded that parental magmas for ore-bearing intrusions had no specific features and were closed to intraplate basalts. Full article

Submarine volcanic-hosted iron oxide deposits are critical archives for reconstructing the interplay between hydrothermal activities and marine redox conditions, yet the genesis of these deposits remains controversial. Here, we present a comprehensive geochronological and geochemical study on the Shikebutai iron deposit in the Western Tianshan, northwestern China, to constrain the mineralization age, the source of iron, and deposit genesis. The stratiform-to-lenticular orebodies are hosted within the Late Carboniferous marine volcanic–sedimentary sequence of the Yishijilike Formation. The iron ores consist primarily of hematite and quartz, with minor siderite and barite, exhibiting massive to locally banded textures. SHRIMP zircon U-Pb dating of the overlying andesite yields an age of 315.8 ± 1.5 Ma, consistent with the Sm–Nd isochron age of the iron ore samples (319 ± 26 Ma), precisely constraining the mineralization age to the Late Carboniferous (ca. 315–320 Ma). The geochemical compositions of the iron ore samples indicate negligible syn-depositional detrital contamination, as evidenced by low Al₂O₃ (<1.00 wt%) and TiO₂ (<0.20 wt%) contents. Low abundances of trace elements, including Sr (0.33–31.18 ppm), Hf (0.05–1.77 ppm) and Rb (1.49–39.02 ppm), further support the minimal detrital influence. Geochemical signatures, such as pronounced positive Eu anomalies (Eu/Eu = 1.62–7.12, mean 4.14), LREE enrichment ((La/Yb) _(PAAS) = 0.58–4.78), and near-chondritic Y/Ho ratios (mean 28.5), suggest a significant high-temperature (>250 °C) hydrothermal contribution. Moreover, the ε_Nd(t) values of iron ore samples (+1.99 to +2.93) are comparable to those of coeval andesites (+2.75 to +3.44) but exceed those of associated metasiltstones (+0.41 to +0.95), suggesting that ore-forming materials were derived from hydrothermal fluids leaching juvenile crust. The Shikebutai iron deposit exhibits geochemical and mineralogical similarities to modern Red Sea and East Pacific Rise metalliferous sediments, establishing the deposit as a product of active vent-proximal hydrothermal systems rather than marine chemical sediments such as banded iron formations. Full article

The horst and graben system in Western Anatolia lies on the eastern boundary of the Aegean extensional system, one of the most active extensional zones in the world. The Şahinali coal basin is located south of the Büyük Menderes Graben, which is part of this system. This study examines the rare earth elements and yttrium (REY) geochemistry, accumulation conditions, and economic potential of the Şahinali coals. Compared to world coals, the REE concentration in Şahinali coals (208.3 ppm) is quite high, and all REY groups are slightly enriched. Light REY (LREY) is dominant compared to medium REY (MREY) and heavy REY (HREY). The most abundant element in this group is Ce, reaching a concentration of 123.3 ppm. REY distribution patterns indicate H-type enrichment in most samples and, to a lesser extent, M-H-type enrichment. Element ratios (Al₂O₃/TiO₂, TiO₂/Zr, La/Sc, Co/Th) and REY anomalies (Ce, Eu, Gd) indicate that the sedimentary input is predominantly derived from felsic rocks, with limited intermediate to mafic contributions. SEM-EDS findings and correlation analyses indicate that REY are predominantly associated with aluminosilicate minerals. LREY-Th and MREY/HREY-Y relationships are supported by monazite and Y-rich illitic K-aluminosilicates. Paleoenvironmental indicators (V/Cr, Ni/Co, U/Th, Sr/Cu, Rb/Sr, Sr/Ba) indicate that the coal accumulated under oxic–suboxic, warm and humid conditions. The average REY oxide (REO) content slightly exceeds the commonly cited 1000 ppm screening threshold for coal ash. The majority of samples contain elevated proportions of critical REY (30.7%–54.3%) and show promising outlook coefficients (C_outl: 0.8–1.7). Together, these results indicate a favourable compositional signature for preliminary REY resource screening in the Şahinali coals, particularly with respect to elements relevant for high-technology applications. Full article

Tungsten trioxide (WO₃) exhibits complementary optical and electrical responses toward hydrogen, yet the interplay between interfacial stress, crystal phase stabilization, and gasochromic/chemiresistive performance remains insufficiently understood. In this work, WO₃ films were grown on four single-crystal oxide substrates to systematically tune interfacial stress and thereby modulate the resulting crystal phase, microstructure, and exposed facets. θ–2θ diffraction revealed that WO₃ adopts a monoclinic phase on YAlO₃ and SrLaAlO₄, whereas a high-temperature orthorhombic phase is stabilized on LaAlO₃ (LAO) and SrTiO₃ due to stronger interfacial constraint. Compared with the amorphous quartz reference, the single-crystal substrates significantly enhanced both gasochromic and chemiresistive responses. In particular, the orthorhombic WO₃/LAO film exhibited an electrical response of 1.97 × 10⁴ (R_air/R_H2), an optical transmittance changed of 12.7%, and an electrical response time of 1 s toward 2% H₂ at 80 °C, far exceeding the monoclinic and amorphous counterparts. The combined effects of stress-induced phase stabilization, film orientation, and hydrogen diffusion pathways are shown to govern the non-monotonic sensing trends among different substrates. These findings elucidate the structural origin of hydrogen sensitivity in WO₃ and provide guidance for stress-engineered design of high-performance gasochromic and chemiresistive sensors. Full article

The Chaluo granite is situated in the middle section of the Yidun magmatic arc in western Sichuan Province, China. It holds great significance for the study of the geological evolution of the Paleo-Neotethys tectonic belts. The Chaluo granite mainly consists of alkaline feldspar, quartz, and biotite, with a small amount of apatite. LA-ICP-MS zircon U-Pb dating yielded crystallization ages of (87 ± 3) Ma for the Chaluo granite, indicating its formation in the Late Cretaceous. Elemental geochemical testing results showed that the Chaluo granite exhibits I-type granite characteristics. It has undergone significant fractional crystallization processes, with high SiO₂ contents (72.83–76.63 wt%), K (K₂O/Na₂O = 1.33–1.53), Al₂O₃ (Al₂O₃ = 12.24–13.56 wt%, A/CNK = 0.91–1.08), and a high differentiation index (DI = 88.91–92.49). Notably, the MgO contents were low (0.10–0.26 wt%), and there were significant depletions of Nb, Sr, Ti, and Eu, while Rb, Pb, Th, U, Zr, and Hf were significantly enriched. The total rare earth element (REE) contents were relatively low (211–383 ppm), showing significant light REE (LREE) enrichment (LREE/HREE = 4.46–5.57) and a pronounced negative Eu anomaly (δEu = 0.09–0.17). In situ zircon Hf analyses, combined with ²⁰⁶Pb/²³⁸U ages, gave ε_Hf(t) values ranging from −3.8 to 1.72 and two-stage Hf ages (t_DM2) of 875–1160 Ma. Together with the S and Pb isotope compositions of the Chaluo granite, its magma likely originated from the partial melting of Middle–Neoproterozoic sedimentary rocks enriched in biogenic S. The tectonic-setting analysis indicates that the Chaluo granite formed in a post-orogenic intracontinental extensional environment. This environment was triggered by the northward subduction-collision of the Lhasa block, followed by slab break-off and the upwelling of the asthenosphere in the Neo-Tethys orogenic belt. We propose that the Paleo-Tethys tectonic belt was influenced by the Neo-Tethys tectonic activity, at least in the Yidun magmatic arc region during the Late Cretaceous. Full article

Haigou deposit, located in Dunhua City, southeast Jilin Province, NE China, is a large-scale gold deposit. The gold ore body is categorized into two types: quartz-vein type and altered rock type, with the quartz-vein type being predominant. The vein gold ore body primarily occurs within the monzonite granite and monzonite rock mass in the Haigou area and is controlled by fault structures trending northeast, northwest, and near north-south. In order to constrain the age and tectonic setting of quartz vein-type gold mineralization, we conducted a detailed underground investigation and collected samples of monzonite granite and pyroxene diorite porphyrite veins related to quartz-vein-type gold mineralization for LA-ICP-MS zircon U-Pb dating and whole-rock main trace element data testing to confirm that monzonite granite is closely related to gold mineralization. Pyroxene diorite porphyry and gold mineralization were found in parallel veins. The zircon U-Pb weighted mean ages of monzonite and pyroxene diorite porphyrite veins are 317.1 ± 3.5 Ma and 308.8 ± 3.0 Ma, respectively, indicating that gold mineralization in monzonite, pyroxene diorite porphyrite veins, and quartz veins occurred in the Late Carboniferous. The monzonite granite and pyroxene diorite porphyrite veins associated with quartz vein-type gold mineralization have high SiO₂, high K, and high Al₂O₃ and are all metaluminous high-potassium calc-alkaline rock series. Both of them are relatively enriched in light rare earth elements (LREE) and macroionic lithophile elements (LILE: Rb, Ba, K, etc.), but deficient in heavy rare earth elements (HREE) and high field strength elements (HFSE: Nb, Ta, P, Ti, etc.), the monzonitic granite Eu is a weak positive anomaly (δEu = 1.15–1.46), the pyroxene diorite porphyre dyke Eu is a weak positive anomaly (δEu = 1.09–1.13), and the Nb and Ta are negative anomalies. The Th/Nb values are 0.28–0.73 and 1.48–2.05, and La/Nb are 2.61–4.74 and 4.59–5.43, respectively, suggesting that diagenetic mineralization is the product of subduction in an active continental margin environment. In recent years, scholarly research on Sr, Nd, and Pb isotopes in Haigou rock masses has indicated that the magmatic source region in the Haigou mining areas is complex. It is neither a singular crustal source nor a mantle source but rather a mixed crust-mantle source, primarily resulting from the partial melting of lower crustal materials, with additional contributions from mantle-derived materials. In summary, the metallogenic characteristics, chronology data, geochemical characteristics, and regional tectonic interpretation indicate that at least one phase of magmatic-hydrothermal gold mineralization was established in the Late Carboniferous as a result of the subduction of the Paleo-Asian ocean plate at the northern margin of the North China Craton. Full article

The Kongco area of Nima in the northern part of the Lhasa terrane has a suite of alkaline granitic porphyry dykes associated with Early Cretaceous granites and accompanied by Cu/Mo mineralization. LA-ICP-MS ²⁰⁶Pb/²³⁸U zircon geochronology performed on the dykes produced an age of 104.15 ± 0.94 Ma (MSWD = 0.98), indicating the Early Cretaceous emplacement of the dykes. The dykes exhibit high silica (SiO₂ = 76.22~77.90 wt.%), high potassium (K₂O = 4.97~6.21 wt.%), high alkalinity (K₂O + Na₂O = 8.07~8.98 wt.%), low calcium (CaO = 0.24~0.83 wt.%), low magnesium (MgO = 0.06~0.20 wt.%), and moderate aluminum content (Al₂O₃ = 11.93~12.45 wt.%). The Rieterman index (σ) ranges from 1.93 to 2.34. A/NK (molar ratio Al₂O₃/(Na₂O + K₂O)) and A/CNK (molar ratio Al₂O₃/(CaO + Na₂O + K₂O)) values of the dykes range from 1.06 to 1.18 and 0.98 to 1.09, respectively. The dykes are relatively enriched in Rb, Th, U, K, Ta, Ce, Nd, Zr, Hf, Sm, Y, Yb, and Lu, and they show a noticeable relative depletion in Ba, Nb, Sr, P, Eu, and Ti, as well as an average differentiation index (DI) of 96.42. The dykes also exhibit high FeO_T/MgO ratios (3.60~10.41), Ga/Al ratios (2.22 × 10⁻⁴~3.01 × 10⁻⁴), Y/Nb ratios (1.75~2.40), and Rb/Nb ratios (8.36~20.76). Additionally, they have high whole-rock Zr saturation temperatures (884~914 °C), a pronounced Eu negative anomaly (δEu = 0.04~0.23), and a rightward-sloping “V-shaped” rare earth element pattern. These characteristics suggest that the granitic porphyry dykes can be classified as A2-type granites formed in a post-collisional tectonic environment and that they are weakly peraluminous, high-potassium, and Calc-alkaline basaltic rocks. Positive ε_Hf(t) values = 0.43~3.63 and a relatively young Hf crustal model age (T_DM2 = 826~1005 Ma, ⁸⁷Sr/⁸⁶Sr ratios = 0.7043~0.7064, and ε_Nd(t) = −8.60~−2.95 all indicate lower crust and mantle mixing. The lower crust and mantle mixing model is also supported by (²⁰⁶Pb/²⁰⁴Pb)t = 18.627~18.788, (²⁰⁷Pb/²⁰⁴Pb)t = 15.707~15.719, (²⁰⁸Pb/²⁰⁴Pb)t = 39.038~39.110). Together, the Hf, Sr and Pb isotopic ratios indicate that the Kongco granitic porphyry dykes where derived from juvenile crust formed by the addition of mantle material to the lower crust. From this, we infer that the Kongco granitic porphyry dykes are related to a partial melting of the lower crust induced by subduction slab break-off and asthenospheric upwelling during the collision between the Qiangtang and Lhasa terranes and that they experienced significant fractional crystallization dominated by potassium feldspar and amphibole. These dykes are also accompanied by significant copper mineralization (five samples, copper content 0.2%), suggesting a close relationship between the magmatism associated with these dykes and regional metallogenesis, indicating a high potential for mineral exploration. Full article

The Yidun island arc was formed in response to the Late Triassic westward subduction of the Ganzi–Litang oceanic plate, a branch of the Paleo-Tethys Ocean. The Zhongdian arc, located in the south of the Yidun island arc, has relatively large number of porphyry (skarn) type Cu–Mo ± Au polymetallic deposits, the largest of which is the Pulang Cu (–Mo–Au) deposit with proven Cu reserves of 5.11 Mt, Au reserves of 113 t, and 0.17 Mt of molybdenum. However, the relationship between mineralization and the potassic alteration zone, phyllic zone, and propylitic zone of the Pulang porphyry deposit is still controversial and needs further study. Titanite (CaTiSiO₅) is a common accessory mineral in acidic, intermediate, and alkaline igneous rocks. It is widely developed in various types of metamorphic rocks, hydrothermally altered rocks, and a few sedimentary rocks. It is a dominant Mo-bearing phase in igneous rocks and contains abundant rare earth elements and high-field-strength elements. As an effective geochronometer, thermobarometer, oxybarometer, and metallogenic potential indicator mineral, titanite is ideal to reveal the magmatic–hydrothermal evolution and the mechanism of metal enrichment and precipitation. In this paper, major and trace element contents of the titanite grains from different alteration zones were obtained using electron probe microanalysis (EPMA) and laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to define the changes in physicochemical conditions and the behavior of these elements during the process of hydrothermal alteration at Pulang. Titanite in the potassic alteration zone is usually shaped like an envelope. It occurs discretely or is enclosed by feldspar, with lower contents of CaO, Al, Sr, Zr and Hf; a low Nb/Ta ratio; high ∑REE + Y, U, Th, Ta, Nb, and Ga content; and high FeO/Al₂O₃ and LREE/HREE ratios. This is consistent with the characteristics of magmatic titanite from fresh quartz monzonite porphyry in Pulang and other porphyry Cu deposits. Titanite in the potassium silicate alteration zone has more negative Eu anomaly and a higher U content and Th/U ratio, indicating that the oxygen fugacity decreased during the transformation to phyllic alteration and propylitic alteration in Pulang. High oxygen fugacity is favorable for the enrichment of copper, gold, and other metallogenic elements. Therefore, the enrichment of copper is more closely related to the potassium silicate alteration. The molybdenum content of titanite in the potassium silicate alteration zone is 10²–10⁴ times that of the phyllic alteration zone and propylitic alteration zone, while the copper content is indistinctive, indicating that molybdenum was dissolved into the fluid or deposited in the form of sulfide before the medium- to low-temperature hydrothermal alteration, which may lead to the further separation and deposition of copper and molybdenum. Full article

For the first time, inductively coupled plasma mass spectrometry (ICP-MS) was developed for determining the target elemental composition of gadolinium–aluminum garnets with the varying composition Gd_3–xCe_xSc_yAl_5–yO₁₂, where x = 0.01–0.16 and y = 0.25–1.75. This fact has a fundamental importance for obtaining optical ceramics with predictable properties. Using the proposed acid mixture and temperature-time program, microwave digestion of these materials and complete transfer of the sample’s components into solution were possible. Moreover, we estimated the influence of the matrix composition, sample introduction system and collision cell on the limits of determination (LOD) of impurity elements by ICP-MS (Mg, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Y, La, Pr, Nd, Sm, Eu, Tb, Er, Ho, Tm, Yb, and Lu). It has been shown that the conditions of mass spectral analysis proposed in this work provide LOD of target analytes in the range of 1∙10⁻⁶–4.15∙10⁻³ wt.%. The accuracy of the obtained results has been confirmed by the added-found method and by analyzing samples with known chemical composition. The standard deviation of repeatability (S_r) of the developed technique lies in the range from 1 to 6%. The developed analysis method is characterized by sensitivity, robustness and multi-elementality. It has application potential for other optical and ceramic materials of similar composition. Full article

The Carboniferous Benxi Formation in southern Shanxi of North China has significant bauxite resource potential; however, the source of its metallogenic material and its sedimentary environment remain unclear. The microscopy, X-ray diffraction, X-ray fluorescence spectroscopy, and inductively coupled plasma mass spectrometry methods were applied in this study to examine the mineralogical, petrographic, and geochemical characteristics. Geochemical proxies of La/Y, Sr/Ba, Al₂O₃/TiO₂, Zr/Sc, Th/Sc, La/Sc, and Th/Co were analyzed to investigate the paleo-depositional environment and provenance of the aluminum-bearing strata. The findings indicate that diaspores are the primary ore minerals in bauxite, while kaolinite and rutile are the predominant gangue minerals. Both the bauxite and claystone/aluminous rocks exhibit high enrichment in Li, Bi, and U, with relative enrichment in In, Sb, Th, Nb, and Ta. Li is notably concentrated in the claystone/aluminous rocks, reaching up to 1994.00 μg/g, primarily occurring in cookeite and boehmite, while U is highly concentrated in the bauxite. The aluminum-bearing strata were primarily formed under alkaline-reducing conditions, with changes in acidity and alkalinity of the environment during the sedimentary diagenetic process. Marine transgressions significantly impacted the sedimentary environment of the aluminum-bearing strata, and the paleoclimate was characterized as hot and humid. The principal factors contributing to enrichment of aluminum in the sedimentary basin were the in situ weathering of aluminum-rich source rocks and the transport of clastic materials from high-aluminum source rocks. The source rocks were closely associated with intermediate-acidic magmatic rocks and potentially related to the weathering of Ordovician carbonates. Full article

High-silica adakites exhibit specific compositions, as follows: SiO₂ ≥ 56 wt.%, Al₂O₃ ≥ 15 wt.%, Y ≤ 18 ppm, Yb ≤ 1.9 ppm, K₂O/Na₂O ≥ 1, MgO < 3 wt.%, high Sr/Y (≥10), and La/Yb (>10). Devonian I-type adakitic granitoids in the northern Appalachians of New Brunswick (NB, Canada) share geochemical signatures of adakites elsewhere, i.e., SiO₂ ≥ 66.46 wt.%, Al₂O₃ > 15.47 wt.%, Y ≤ 22 ppm, Yb ≤ 2 ppm, K₂O/Na₂O > 1, MgO < 3 wt.%, Sr/Y ≥ 33 to 50, and La/Yb > 10. Remarkably, adakitic intrusions in NB, including the Blue Mountain Granodiorite Suite, Nicholas Denys, Sugar Loaf, Squaw Cap, North Dungarvan River, Magaguadavic Granite, Hampstead Granite, Tower Hill, Watson Brook Granodiorite, Rivière-Verte Porphyry, Eagle Lake Granite, Evandale Granodiorite, North Pole Stream Suite, and the McKenzie Gulch porphyry dykes all have associated Cu mineralization, similar to the Middle Devonian Cu porphyry intrusions in Mines Gaspé, Québec. Trace element data support the connection between adakite formation and slab break-off, a mechanism influencing fertility and generation of porphyry Cu systems. These adakitic rocks in NB are oxidized, and are relatively enriched in large ion lithophile elements, like Cs, Rb, Ba, and Pb, and depleted in some high field strength elements, like Y, Nb, Ta, P, and Ti; they also have Sr/Y ≥ 33 to 50, Nb/Y > 0.4, Ta/Yb > 0.3, La/Yb > 10, Ta/Yb > 0.3, Sm/Yb > 2.5, Gd/Yb > 2.0, Nb + Y < 60 ppm, and Ta + Yb < 6 ppm. These geochemical indicators point to failure of a subducting oceanic slab (slab rollback to slab break-off) in the terminal stages of subduction, as the generator of post-collisional granitoid magmatism. The break-off and separation of a dense subducted oceanic plate segment leads to upwelling asthenosphere, heat advection, and selective partial melting of the descending oceanic slab (adakite) and (or) suprasubduction zone lithospheric mantle. The resulting silica-rich adakitic magmas ascend through thickened mantle lithosphere, with minimal affect from the asthenosphere. The critical roles of transpression and transtension are highlighted in facilitating the ascent and emplacement of these fertile adakitic magmas in postsubduction zone settings. Full article

The Uhelchulu quartz diorite-granodiorite intrusions in Xiwuqi, Inner Mongolia, are exposed along the northwestern margin of the Xilinhot microcontinental block, located within the central and eastern parts of the southeastern Hegenshan suture zone. LA-ICP-MS zircon U-Pb dating yielded crystallization ages of (396 ± 8) Ma for the quartz diorite and (385 ± 5) Ma for the granodiorite, indicating an Early-Middle Devonian magmatic event. The quartz diorite exhibits I-type granite features, characterized by elevated Al₂O₃ (14.33–15.43 wt%), MgO (3.73–5.62 wt%), and Na (Na₂O/K₂O = 1.04–1.44), coupled with low P₂O₅ (0.15–0.20 wt%) and TiO₂ (0.73–0.99 wt%). Trace element patterns show relative enrichments in Rb, Th, U, and Pb, while Nb, Ta, Sr and Ti are relatively depleted. Total REE contents are relatively low (123–178 ppm), with significant LREE enrichment (ΣLREE/ΣHREE = 4.75–5.20), and a non-obvious Eu anomaly (δEu = 0.75–0.84). In contrast, the granodiorite displays S-type granite characteristics, with high SiO₂ (70.48–73.01 wt%), K (K₂O/Na₂O = 1.35–1.83), Al₂O₃ (A/CNK = 1.16–1.31), and a high differentiation index (DI = 76–82). Notably, MgO (1.44–2.24 wt%) contents are low, and significant depletions of Ba, Sr, Ti, and Eu are observed, while Rb, Pb, Th, U, Zr, and Hf are significantly enriched. Total REE contents are relatively low (178–314 ppm), exhibiting significant LREE enrichment (LREE/HREE = 6.17–8.36) and a pronounced negative Eu anomaly (δEu = 0.34–0.49). The overall characteristics point towards an active continental margin arc background for the Uhelchulu intrusions. Previous studies have suggested that the Hegenshan ocean continuously subducted northward from the Early Carboniferous to the Late Permian, but there is a lack of evidence for its geological evolution during the pre-Early Carboniferous. Therefore, this paper provides a certain basis for studying the geological evolution during the pre-Early Carboniferous in the Hegenshan ocean. We preliminarily believed that the Hegenshan ocean underwent a southward subduction towards the Xilinhot microcontinental block in the Xiwuqi area, at least from the Early Devonian to the Middle Devonian and the Hegenshan ocean may might have undergone a shift in subduction mechanism during the Late Devonian or Early Carboniferous. Full article

Himalayan leucogranite is an excellent target for understanding the orogenic process of the India–Asia collision, but its origin and tectonic significance are still under debate. An integrated study of geochronology, geochemistry, and in situ Sr-Nd-Hf isotopes was conducted for a tourmaline-bearing leucogranite in the eastern Tethyan Himalaya using LA-ICP-MS, X-ray fluorescence spectroscopy, and ICP-MS and LA-MC-ICP-MS, respectively. LA-ICP-MS U-Pb dating of zircon and monazite showed that it was emplaced at ~19 Ma. The leucogranite had high SiO₂ and Al₂O₃ contents ranging from 73.16 to 73.99 wt.% and 15.05 to 15.24 wt.%, respectively. It was characterized by a high aluminum saturation index (1.14–1.19) and Rb/Sr ratio (3.58–6.35), which is characteristic of S-type granite. The leucogranite was enriched in light rare-earth elements (LREEs; e.g., La and Ce) and large ion lithophile elements (LILEs; e.g., Rb, K, and Pb) and depleted in heavy rare-earth elements (e.g., Tm, Yb, and Lu) and high field strength elements (HFSEs; e.g., Nb, Zr, and Ti). It was characterized by high I Sr (t) (0.7268–0.7281) and low ε Nd (t) (−14.6 to −13.2) and ε Hf (t) (−12.6 to −9.47), which was consistent with the isotopic characteristics of the Higher Himalayan Sequence. Petrogenetically, the origin of the leucogranite is best explained by the decompression-induced muscovite dehydration melting of an ancient metapelitic source within the Higher Himalayan Sequence during regional extension due to the movement of the South Tibetan Detachment System (STDS). The significantly high lithium and beryllium contents of the leucogranite and associated pegmatite suggest that Himalayan leucogranites possess huge potential for lithium and beryllium exploration. Full article

The ground state of correlated electrons in complex oxide films can be controlled by applying epitaxial strain, offering the potential to produce unexpected phenomena applicable to modern spintronic devices. In this study, we demonstrate that substrate-induced strain strongly affects the coupling mode of interfacial magnetic moments in a ferromagnetic (FM)/antiferromagnetic (AFM) system. In an epitaxial bilayer comprising AFM LaFeO₃ (LFO) and FM La_0.7Sr_0.3MnO₃ (LSMO), samples grown on a LaAlO₃ (LAO) substrate exhibit a larger exchange bias field than those grown on a SrTiO₃ substrate. Our results indicate a transition in the alignment of magnetic moments from perpendicular to collinear due to the large compressive strain exerted by the LAO substrate. Collinear magnetic moments at the LSMO/LFO interface generate strong exchange coupling, leading to a considerable exchange bias effect. Thus, our findings provide a method for tailoring and manipulating the orientations of magnetic moments at the FM/AFM heterogeneous interface using strain engineering, thereby augmenting methods for exchange bias generation. Full article