Acta Geochimica最新文献

The debate regarding whether the Yarlung–Zangbo ophiolite (YZO) on the south of the Qinghai-Tibet Plateau, formed in a mid-ocean ridge (MOR) or a supra-subduction zone (SSZ) setting has remained unresolved. Here we present petrological, mineralogical, and geochemical data associated with modeling melting geodynamics of the mantle peridotites from the Purang ophiolite in the western segment of the Yarlung–Zangbo Suture Zone (YZSZ) to explore its tectonic environment. The Purang lherzolites are characterized by the protogranular texture and have abyssal-peridotite-like mineral compositions, including low Cr^# (20–30) and TiO₂ contents (<0.1wt%) in spinel, high Al₂O₃ (2.9wt% – 4.4wt%) and CaO (1.9wt% – 3.7wt%) contents in orthopyroxene and LREE-depletion in clinopyroxene. Compositions of these lherzolites can be modeled by ~11% dynamic melting of the DMM source with a small fraction of melt (~0.5%) entrapped within the source, a similar melting process to typical abyssal peridotites. The Purang harzburgites are characterized by the porphyroclastic texture and exhibit highly refractory mineral compositions such as high spinel Cr^# (40–68), low orthopyroxene Al₂O₃ (<2.2wt%) and CaO (<1.1wt%) contents. Clinopyroxenes in these harzburgites are enriched in Sr (up to 6.0 ppm) and LREE [(Ce)_N = 0.02–0.4], but depleted in Ti (200 ppm, on average) and HREE [(Yb)_N < 2]. Importantly, the more depleted samples tend to have higher clinopyroxene Sr and LREE contents. These observations indicate an open-system hydrous melting with a continuous influx of slab fluid at a subduction zone. The modeled results show that these harzburgites could be formed by 19% – 23% hydrous melting with the supply rate of slab fluid at 0.1%–1%. The lower clinopyroxene V/Sc ratios in harzburgites than those in lherzolites suggest a high oxidation stage of the melting system of harzburgites, which is consistent with a hydrous melting environment for these harzburgites. It is therefore concluded that the Purang ophiolite has experienced a transformation of tectonic setting from MOR to SSZ.

The studies on hydrothermal alteration-induced effects in surface and subsurface rocks provide useful information in the characterization and exploitation of a geothermal reservoir. Generally, these studies are based on traditional, and reliable methods like petrography (primary and secondary minerals, and grade of alteration), and geochemistry (mobility of elements, changes in mass and concentration of elements, and fluid inclusions). Recently, apart from these established methods, some methods based on the geochemical (Chemical Index of Alteration, CIA; Weathering Index of Parkar, WIP; Loss on Ignition, LOI; and Sulfur, S) and rock magnetic properties (magnetic susceptibility, χlf; and percentage frequency-dependent susceptibility, χfd%) are also being applied in the identification of whether a rock is an altered or a fresh one. The Acoculco Geothermal Field (AGF), Mexico, is characterized by high temperature and very low permeability, and it is considered a promissory Enhanced Geothermal System. The following changes are observed in the rocks as a result of an increase in hydrothermal alteration: (1) an increase in CIA, LOI, and S values, and a decrease in WIP; (2) an increase in quartz and quartz polymorph minerals (silicification), and clay minerals (argillization); and (3) decrease in χlf values. At AGF, the most altered surface acid rocks are characterized by entirely quartz and its polymorphs, and clay minerals. The present study also indicates the applicability of the binary plots of major elements (felsic vs mafic component) and rock magnetic parameters (χlf vs. χfd%). The rock with χfd% value of 2–10 and χlf value < 0.5 × 10^–6 m³ kg⁻¹ indicate the presence of single domain and stable single domain grains, which in turn suggests that it is an altered rock. These methods are simple to apply, rapid, reliable, and have the potential to become effective tools for the identification of hydrothermally altered rocks during the initial stage of geothermal exploration.

It is well-known that the equilibrium isotope fractionation of mercury (Hg) includes classical mass-dependent fractionations (MDFs) and nuclear volume effect (NVE) induced mass-independent fractionations (MIFs). However, the effect of the NVE on these kinetic processes is not known. The total fractionations (MDFs + NVE-induced MIFs) of several representative Hg-incorporated substances were selected and calculated with ab initio calculations in this work for both equilibrium and kinetic processes. NVE-induced MIFs were calculated with scaled contact electron densities at the nucleus through systematic evaluations of their accuracy and errors using the Gaussian09 and DIRAC19 packages (named the electron density scaling method). Additionally, the NVE-induced kinetic isotope effect (KIE) of Hg isotopes are also calculated with this method for several representative Hg oxidation reactions by chlorine species. Total KIEs for ²⁰²Hg/¹⁹⁸Hg ranging from − 2.27‰ to 0.96‰ are obtained. Three anomalous ²⁰²Hg-enriched KIEs (δ²⁰²Hg/¹⁹⁸Hg = 0.83‰, 0.94‰, and 0.96‰,) caused by the NVE are observed, which are quite different from the classical view (i.e., light isotopes react faster than the heavy ones). The electron density scaling method we developed in this study can provide an easier way to calculate the NVE-induced KIEs for heavy isotopes and serve to better understand the fractionation mechanisms of mercury isotope systems.

The tectonic evolution and crustal accretion process of the North Qilian Orogenic Belt (NQOB) are still under debate because of a lack of integrated constraints, especially the identification of the tectonic transition from arc to initial collision. Here we present results from zircon U–Pb geochronology, whole-rock geochemistry, and Sr–Nd–Pb isotope geochemistry of the Beidaban granites to provide crucial information for geodynamic evolution of NQOB. Zircon U–Pb dating yields an age of 468 ± 10 Ma for the Beidaban granites and most of the Beidaban samples contain amphibole, are potassium-rich, and have A/CNK values ranging from 0.7 to 0.9, illustrating that the Middle Ordovician Beidaban granites are K-rich, metaluminous, calc-alkaline granitoid. The geochemical characteristics indicate that the Beidaban granites are transitional I/S-type granitoids that formed in an arc setting. The isotopic compositions of initial (⁸⁷Sr/⁸⁶Sr)_i values ranging from 0.70545 to 0.71082 (0.70842 on average) and εNd(t) values ranging from − 10.9 to − 6.7 (− 8.8 on average) with two-stage Nd model ages (T_DM2) of 1.74–2.08 Ga suggest that the Beidaban granites originated from Paleoproterozoic crustal materials. In addition, the initial Pb isotopic compositions (²⁰⁶Pb/²⁰⁴Pb = 19.14–20.26; ²⁰⁷Pb/²⁰⁴Pb = 15.71–15.77; ²⁰⁸Pb/²⁰⁴Pb = 37.70–38.26) and geochemical features, such as high Th/Ta (17.43–30.12) and Rb/Nb (6.01–15.49) values, suggest that the Beidaban granite magma source involved recycled crustal components with igneous rocks. Based on these results in combination with previously published geochronological and geochemical data from other early Paleozoic igneous rocks, we suggest that the timing of the tectonic transition from arc to the initial collision to the final closure of the North Qilian Ocean can be constrained to the Middle-Late Ordovician (ca. 468–450 Ma).

The Pulang giant porphyry Cu-Mo polymetallic deposit is located in the Zhongdian area in the center of the Sanjiang Tethys tectonic domain, which was formed by the westward subduction of the Garze-Litang oceanic slab beneath the Zhongza massif. Chalcopyrite-pyrrhotite-pyrite-molybdenite occurs as disseminations, veins, veinlets, and stockworks distributed in the K-silicate alteration zone in the monzonite porphyry, which is superimposed by propylitization. The chemical compositions of biotite and amphibole analyzed by electron probe microanalysis (EPMA) indicate that the ore-forming magma and exsolved fluids experienced a continuous decrease in the oxygen fugacity (fO₂). Primary amphibolite and biotite (type I) crystallized at relatively high temperatures (744–827 °C) and low fO₂ (logfO₂ = − 12.26 to − 11.91) during the magmatic stage. Hydrothermal fluids exsolved from the magma have a relatively lower temperature (621–711 °C) and fO₂ (logfO₂ = − 14.36 to − 13.32) than the original magma. In addition, the presence of a high abundance of pyrrhotite and an insufficiency of primary magnetite and sulfate in the ore (i.e., anhydrite and gypsum) indicate that the deposit may be a reduced porphyry deposit. Magma and fluid fO₂ results, combined with previous research on magmatic fO₂ at the Pulang deposit, indicate that the magma associated with the reduced Pulang ore assemblages was initially generated as a highly oxidized magma that was subsequently reduced by sedimentary rocks of the Tumugou Formation.

The Gysian ophiolite of NW Iran is located at the intersection of the ophiolite belts of SE Turkey, NE Iraq, and Iran, and provides the opportunity to investigate the preserved subduction and obduction history of an important tectonic site that has not previously been studied. The serpentinized peridotites of the Gysian ophiolite contain the assemblage lizardite + chrysotile + spinel/Mg-spinel with relict clinopyroxene (diopside) and very rare relict orthopyroxene and olivine. The compositions of clinopyroxenes and spinels are more consistent with the formation of the inferred protolith harzburgites in a fore-arc or supra-subduction zone instead of an abyssal environment. The Gysian ophiolite is a remnant of the Neo-Tethyan arc-ophiolitic system and records shallow subduction (< 50 km, indicated by the absence of antigorite) in the Late Cretaceous to Paleocene before obduction along thrust faults over the continental margin. We review the spatial trends of the metamorphic grade of the Neo-Tethyan ophiolites in this region and provide detailed information about the petrology and mineral chemistry of the Gysian ophiolite.

Hydraulic fracturing is an effective technology for hydrocarbon extraction from unconventional shale and tight gas reservoirs. A potential risk of hydraulic fracturing is the upward migration of stray gas from the deep subsurface to shallow aquifers. The stray gas can dissolve in groundwater leading to chemical and biological reactions, which could negatively affect groundwater quality and contribute to atmospheric emissions. The knowledge of light hydrocarbon solubility in the aqueous environment is essential for the numerical modelling of flow and transport in the subsurface. Herein, we compiled a database containing 2129 experimental data of methane, ethane, and propane solubility in pure water and various electrolyte solutions over wide ranges of operating temperature and pressure. Two machine learning algorithms, namely regression tree (RT) and boosted regression tree (BRT) tuned with a Bayesian optimization algorithm (BO) were employed to determine the solubility of gases. The predictions were compared with the experimental data as well as four well-established thermodynamic models. Our analysis shows that the BRT-BO is sufficiently accurate, and the predicted values agree well with those obtained from the thermodynamic models. The coefficient of determination (R²) between experimental and predicted values is 0.99 and the mean squared error (MSE) is 9.97 × 10⁻⁸. The leverage statistical approach further confirmed the validity of the model developed.

The Yangla Cu skarn deposit is located in the central part of the Jinshajiang Suture Zone, southwest China, with a total reserve of 150 Mt Cu @ 1.03%. The newly discovered antimony orebodies at the depth of Yangla are strictly controlled by the stratum, structure, and lithology, which are lenticular and vein-like within the marble fracture zone, which can provide a window into multistage mineralization and ore genesis at Yangla. Mineralization can be divided into three types, Cu–Pb–Zn (skarn) pyrite, galena, and sphalerite, Cu (porphyry) chalcopyrite and pyrite, and Sb (hydrothermal) stibnite and pyrite. The mineral assemblages were stibnite + pyrite + calcite + quartz ± minor scheelite in antimony ores. This study presents quantitative measurements of the trace element compositions of pyrite and stibnite from the Yangla antimony ores. Analysis of pyrite with electron probe microanalysis (EPMA) showed enrichment in Co, Ni, Sb, As, and Mo, and deficit in its S and Fe contents when compared to the stoichiometric concentrations of S and Fe in pyrite. The Sb-related pyrite may belong to sedimentary-reworked genesis and may be modified by hydrothermal fluids, thereby presenting a certain difference (i.e., crystal morphology, texture, and chemical composition) compared to the skarn and porphyry Cu-related pyrite in the Yangla Cu skarn deposit. Analysis of stibnite with EPMA and inductively coupled plasma-mass spectrometry showed enrichment in As, Pb, Sn, Pb, Cu, and Zn, and presented much higher Sb contents and slightly lower S contents when compared to the stoichiometric concentrations of Sb and S in stibnite. Statistical analysis of the stibnite trace elements showed correlations for the elemental pairs Cu–Pb, As–Sb, and Sn–Pb, and the coupled substitution equations Sb³⁺ ↔ Cu⁺ + Pb²⁺, Sb³⁺ ↔ As³⁺, and Sn²⁺ ↔ Pb²⁺ may be the major factors governed the incorporating Cu, Pb, As and Sn within the stibnite. Moreover, this study preliminary shows that the antimony mineralization may belong to a carbonate replacement hydrothermal genesis at Yangla.

The petrographic and geochemical attributes of the Oligocene Barail Group of rocks are used to decipher the likely source area(s) or tectonic domains, as this sequence of rocks was deposited in a foreland basin governed by orogenic domain, namely the North-east Arunachal Himalayas. The river system that gave rise to the Brahmaputra River (Yarlung-Tsangpo), which flowed through several tectonic domains of the Himalayan ranges, primarily from Bomi-Chayu, Gangadese Granitoid, Higher Himalayan Leucogranites, and Namche Barwa into the proto Bengal Basin now a part of Assam Arakan Basin and Naga Schuppen Belt, was the main source of the sandstone formation of the Barail Group. The purpose of sandstone petrography, which combines modal analysis with XRF (Major Oxides) and HR-ICP-MS (Trace & Rare Earth Elements) research, is to identify the type of source rock(s), their weathering pattern, and its paleo-environmental circumstances. These sandstones were formed from recycled orogen and include lithic and sublithic arenite variants with advanced texture and chemical maturity. The sediments were felsic (Th/Co: 1.38, Cr/Th: 9.78, La/Lu: 11.58, Th/Sc: 0.99, Eu/Eu*: 0.66, La/Sc: 3.05, La/Co: 4.18), with contributions from intermediate source rocks and low-rank metamorphics deposited in an active continental margin to a continental island arc setting. Climatic conditions impacted the sediments of Barails, characterised by being warm and semi-humid to humid which resulted in moderate to a high degree of chemical weathering, as shown by weathering indices like CIA (79.14), PIA (85.47), CIW (86.9), WIP (32.50), ICV (0.71), and Th/U (6.03), which were further additionally supported by C-Value (1.01), PF (1.20), Sr/Cu (2.04), and Rb/Sr (0.97).