Mineral Textures Research Articles

Petrogenesis of the Scapolite‐Bearing Kongurblak Shear Zone, Chinese Southwestern Tianshan: Implications for Rock‐Buffered Fluid Flow Migration During Orogeny

ABSTRACTIn the lower Kongurblak River, Chinese SW Tianshan, scapolite was first found in a narrow shear zone (the Kongurblak shear zone, KSZ), consisting of variably mylonitized sedimentary rocks, including marble, meta‐sandstone and felsic–marly phyllonite. These rocks show varying scapolite textures and modes (from less than 1% to 15%), as a sporadic fine‐grained matrix phase, porphyroblasts with abundant inclusions, or blocky aggregates. The Cl content of scapolite (0.90–2.79 wt.%) varies between different rock types, which is higher in meta‐sandstone and marble than in felsic–marly phyllonite. Rare patchy lower Cl domains of scapolite and Ba zoning of K‐feldspar in meta‐sandstone and Cl zoning of porphyroblastic scapolite in marly phyllonite suggest pulsed fluid circulation. P–T estimates, thermodynamic modelling and mineral textures indicate scapolite formation through metasomatizing sodic feldspar and/or metamorphic reactions at amphibolite‐facies conditions (470°C°C–600°C and 3–7 kbar). These findings suggest the NaCl–CO2–H2O fluids in the KSZ stem from an external source, not from evaporitic horizons, at ~200 Ma by apatite U–Pb dating. The chlorinity and X (CO2) values of fluids, calculated based on the chemistry of the assemblage scapolite–biotite and T–X (CO2) diagrams, correlate well with specific rock types they traverse, which show different mineral modes and compositions, prograde reactions, structural permeability and host rock cavities. This indicates that the chemistry of medium‐grade infiltrative fluids in shear zones is strongly rock‐buffered, with crucial implications for orogenic metallogenesis in specific rock types. Evidence that the lithologies within the KSZ and their tectonometamorphic histories are distinct from those of the two bounding metamorphic units suggests they represent exotic sedimentary blocks transported over long distances within a large‐scale mélange, also providing new constraints on the tectonic collage of the Chinese SW Tianshan.

Hydrothermal mineral replacement of bastnäsite by rhabdophane and monazite: effects of temperature on mineralogy, REE immobilisation, and fractionation

The rare-earth elements (REEs, La–Lu, Y) are essential for the development of renewable technologies. Bastnäsite (REECO3F) is a common REE ore mineral that is often subject to hydrothermal alteration at all crustal levels. Mechanisms of hydrothermal bastnäsite alteration therefore govern the evolution of REE deposits, though these mechanisms remain poorly understood. This experimental work investigates the hydrothermal replacement of bastnäsite by rhabdophane (REEPO4∙xH2O, x = 0–1) and monazite (REEPO4) in phosphatic fluids. Two temperature-dependent alteration pathways were identified; both follow the coupled dissolution-reprecipitation (CDR) mechanism. At 90 °C, bastnäsite was replaced by highly-porous metastable rhabdophane which was then replaced by monazite, forming an inner layer of rhabdophane and an outer layer of monazite. At 220 °C, bastnäsite was replaced directly by monazite. Although replacement initiated more quickly at 220 °C, greater overall replacement occurred at 90 °C (~ 61 wt.% after 500 h, compared to ~ 13 wt.% at 220 °C) due to surface passivation by monazite at 220 °C. Geochemical analyses showed REE fractionation during bastnäsite alteration. At 90 °C, rhabdophane was enriched in heavy REEs (Eu–Lu, Y), likely due to the evolving fluid chemistry, while at 220 °C secondary monazite was enriched in Sm and Ho compared to bastnäsite. These results indicate that: 1) the hydrothermal alteration of bastnäsite by rhabdophane and monazite in ore deposits leads to REE immobilisation, with little net loss of REEs to solution; 2) rhabdophane is metastable relative to monazite at 90 °C, and; 3) variable temperatures can cause different mineral textures and REE fractionation trends during hydrothermal alteration and mineral replacement.

Differential mineral diagenetic evolution of lacustrine shale: Implications for CO2 storage

Understanding the differential diagenetic evolution of different lithofacies is essential for assessing the spatial development of shale reservoirs. These insights are crucial in predicting sealing integrity and storage capacity for sequestered CO2. In this study, we examined seven wells from the Cretaceous Qingshankou Formation in the Songliao Basin, China, with vitrinite reflectance (Ro) values ranging from 0.60 % to 1.62 %. Thin section-based petrographic observations, coupled with QEMSCAN analysis, were used to classify the different lithofacies. X-ray diffraction (XRD) analysis of clay minerals, field emission scanning electron microscope (FE-SEM), and energy-dispersive spectrum (EDS) analyses were employed to analyze the mineral textures, pore types, and diagenetic pathways. The results showed that early diagenetic mineral phases include calcite cement (1st phase), framboidal and microcrystalline pyrite, ferroan and non-ferroan dolomite. Intermediate diagenetic mineral phases were marked by illitization of smectite, chlorite formed by chloritization of smectite and alteration of K-feldspar, and the formation of authigenic albite and quartz, calcite cement (2nd phase) and ankerite. Given the higher potential reaction rate of CO2-fluid‑carbonate systems, we propose that the lithofacies dominated by carbonate minerals are not effective for CO2 storage, even in short-term. In contrast, lithofacies rich in feldspar and clay minerals are likely to be more effective for long-term CO2 storage.

Occurrence and enrichment of cobalt and nickel in the Yindongshan ultramafic–mafic intrusion-hosted iron deposit, western Hubei Province, China

The Yindongshan iron deposit in western Hubei Province of China is hosted within Ordovician ultramafic–mafic intrusions. Recent field geological surveys have detected cobalt (Co) and nickel (Ni) enrichment within the Yindongshan clinopyroxenite, suggesting good potential for subeconomic Co-Ni mineralization. This study investigated the occurrence modes and enrichment processes of Co and Ni in the Yindongshan deposit through field geology and in situ analysis of the rock texture, geochronology, and geochemistry of sulfides, Fe-Ti oxides, and silicate minerals. The Yindongshan clinopyroxenites were emplaced at 440.2 ± 7.2 Ma via titanite LA-ICP-MS U-Pb dating, and underwent extensive post-magmatic metamorphism at 401.2 ± 8.6 Ma via apatite U-Pb dating. This metamorphism led to the widespread formation of amphibole via the replacement of clinopyroxene. Subsequently, hydrothermal epidote-albite veins, calcite-pyrite veins, and later actinolite veins developed. Pyrites from both clinopyroxenites and calcite veins show limited δ34S variations from −5.4 ‰ to −1.2 ‰, suggesting a magmatic sulfur source. Late-vein actinolites display geochemical characteristics distinct from those of amphiboles, indicating possible involvement of external fluids. LA–ICP–MS trace element results reveal a general increase in Co and Ni contents from silicate minerals and Fe-Ti oxides to pyrite and from earlier-crystallized coarse-grained clinopyroxenite to later medium- to fine-grained clinopyroxenite. The highest Co and Ni contents observed in pyrite from coarse-grained clinopyroxenite suggest their preferential incorporation into early sulfide minerals and then progressively depleted through magmatic evolution such as fractional crystallization. The positive correlation between Co and Ni with Fe in pyrite, along with the consistent parallel time-resolved LA–ICP–MS depth profiles among different mineral phases, indicates that isomorphic substitution occurred in pyrite. In silicate minerals, the Co and Ni contents increase from pyroxene, amphibole, to actinolite, with almost no Co or Ni present in epidote. The elevated Co and Ni contents in metamorphic amphiboles are attributed to their remobilization from magmatic pyrite to newly formed amphiboles. During the late hydrothermal phase, external fluids might transport additional Co and Ni, contributing to higher concentrations in late actinolite veins. In general, Co and Ni in the Yindongshan iron deposit are primarily hosted in sulfide minerals and can be remobilized during regional metamorphism and metasomatism. Thus, magmatic iron or iron–titanium oxide deposits hosted by mafic–ultramafic intrusions with sulfide mineralization may serve as promising targets for further Co-Ni exploration.

Metal remobilization at the Nibao gold deposit in Youjiang basin, SW China: Implications from mineral texture, trace element and sulfur isotope compositions of sulfides and TiO2 polymorphs

Multistage mineralization overprinting is important for the formation of giant hydrothermal gold deposits. The Youjiang basin in SW China has undergone at least three major deformation phases in the Mesozoic, but their relationship with the large-scale gold accumulation in the region remains enigmatic. Here, we study the large Nibao gold deposit (reserve > 70 t Au) in the northern part of the basin, which has both fault-controlled and stratabound orebodies. We identified a pre-ore stage and syn-ore stage including four tectono-hydrothermal (T-H) substages (i.e., T-H stage 1, 2, 3 and 4) for the local mineralization at Nibao. The pre-ore stage is dominated by coarse-grained pyrite coexisting with TiO2 polymorphs in the Middle-Late Permian basaltic rocks. The T-H substage 1 is characterized in that the sedimentary pyrites are brecciated in bedding-parallel faults. Fluorination and silicification occur in the T-H substage 2, which is re-brecciated at the T-H substage 3 forming the highest gold grade ore in high-angle thrust fault. The T-H substage 4 presents as fault reactivation within minor calcite and pyrite deposition. Mineralogy and in-situ trace element analyses reveal that mineral dissolution and reprecipitation (incl. dolomite, auriferous pyrite and TiO2 polymorphs) is ubiquitous during the multistage tectono-hydrothermal process, and the continuous alteration overprinting may have promoted gold accumulation. This replacement process of different generations of auriferous pyrite is also recorded by their inherited sulfur isotopes, giving a narrow δ34S (−3.1 to + 2.1 ‰) range. Anatase is the main accessory phase of TiO2 polymorphs, as identified with LA-ICP-MS trace element and laser Raman spectroscopic analyses. Moreover, the anatase can been divided into two types (type-I and II) based on their texture, alteration and chemistry. The type-I anatase commonly occurring in the stratabound ore is characterized by higher Zr (mean 1,730 ppm), V (mean 1,412 ppm), and Cr (mean 110 ppm) contents than type-II that coexists with zoned pyrite in the fault-controlled ore (mean 26 ppm, 187 ppm, and 38 ppm, respectively). Additionally, W (mean 636 ppm) and Mg (10,021 ppm) in type-II are much higher than type-I ones (mean 135 ppm W and 476 Mg). These features show that the sedimentary-stage Zr-V-Cr-rich type-I anatase was dissolved via fluid metasomatism, and reprecipitated as the hydrothermal-stage W-Mg-rich and Zr-poor anatase, with gold gradually enriched. Besides, the anatase phase of TiO2 polymorphs also indicates that the Nibao gold deposit was formed under low pressure–temperature condition. Overall, we propose that the Nibao is a Carlin-type gold deposit, dominated by multistage tectono-hydrothermal events.

Magmatic genesis, hydration, and subduction of the tholeiitic eclogite-facies Allalin gabbro (Western Alps, Switzerland)

The Allalin gabbro of the Zermatt-Saas meta-ophiolite consists of variably metamorphosed Mg- to Fe-Ti-gabbros, troctolites, and anorthosites, which are crosscut by basaltic dykes. Field relationships of the various rock types and petrographic studies together with bulk rock and mineral chemical composition data allow the reconstruction of the complete geological history of the Allalin gabbro. With increasing magmatic differentiation, the incompatible element content in clinopyroxene increases (e.g., REEs and Zr by a factor of 5), whereas the Mg# decreases (from 86.4 to 74.6) as do the compatible element contents (e.g., Cr and Ni by factors of 3.5 and 5, respectively). Exhumation to shallower depths led to subsolidus ductile deformation and cooling of the gabbro followed by the intrusion of fine-grained basaltic dykes, which display chilled margins. Bulk rock data of these dykes reveal strong similarities in fluid-immobile trace element patterns to tholeiitic pillow basalts of the Zermatt-Saas and nearby meta-ophiolites. The recalculated REE patterns of the melt in equilibrium with igneous clinopyroxene is very similar to the REE patterns of the mafic dykes, indicating a cogenetic origin of pillow basalts, dykes, and gabbros. Together with the previously determined Jurassic intrusion age of the gabbro, our observations demonstrate that the Allalin gabbro intruded as a tholeiitic magma in a slow spreading MOR environment of the Piemonte-Ligurian ocean of the Alpine Tethys. Subduction of the Allalin gabbro resulted in different eclogitization extents of the Mg-gabbros as a function of variable hydration degrees. Metagabbros with low extents of hydration record incomplete eclogitization; the magmatic mineralogy (olivine + clinopyroxene + plagioclase) is preserved together with disequilibrium textures in the form of reaction coronae surrounding mineral boundaries. Metagabbros with high extents of hydration are completely eclogitized and display pseudomorphic replacement textures of magmatic minerals by eclogite-facies mineral assemblages, which required significant major to trace element transport across mineral domains. The locally variable extents of hydration took place near the sea floor, as recorded by the presence of Cl-apatite (6.28 wt% Cl), and an increase in B concentrations of minerals pseudomorphically replacing olivine (e.g., chlorite with 0.20–0.31 µg/g B and omphacite with 0.22–0.25 µg/g B) compared to magmatic olivine (0.12–0.16 µg/g B). Moreover, the chemical zonation pattern of metamorphic garnet coronae is different in completely eclogitized gabbros and gabbros with relic igneous minerals, in agreement with a main hydration event prior to subduction. The Allalin gabbro therefore represents a classical example of an oceanic gabbro formed in a slow spreading setting in the mid Jurassic that experienced heterogeneous hydration near the sea floor. Paleogene subduction of the gabbro to 70–80 km depth produced variably equilibrated gabbroic eclogites. In eclogite-facies Mg-gabbros, the water-rich minerals chlorite, talc, and chloritoid pseudomorphing magmatic olivine remained stable to these depths, revealing the potential relevance of hydrated Mg-gabbros as a fluid source at subarc depths in subduction zones.

Mineralogical characterization and structural control of the Tadaout-Tizi n’Rsas vein field (eastern Anti-Atlas Morocco)

The Tadaout-Tizi n’Rsas (TTR) polymetallic (Pb, Cu, Zn) vein field, located at the southeastern of the Moroccan eastern Anti-Atlas, is hosted in sedimentary sandstone formations of the Ktaoua Group of the upper Ordovician. These deposits are reported to be late Variscan to Post-variscan in age, and are related to the emplacement of late Permian doleritic magma event outcropping in the Tafilalet region. Structural and paragenetic studies of the TTR mineralization deposit were conducted in order to establish a general model of the mineralization. A two-stage model of the formation of the mineralized veins of the TTR vein field is proposed herein. The first episode is attributed to the late Variscan phase. It is a trantensive regime characterized by the presence of lenticular structures related to the normal dextral movement of the major faults. This episode is coeval with the emplacement and brecciation of the polymetallic mineralization of the TTR vein field (galena, chalcopyrite, sphalerite, and pyrite). The second episode is associated with normal faults, during the extensional phase corresponding to the tectonic relaxation of shortening (Upper Permian) and more probably during the Atlantic rifting. It is characterized by the formation of a banded texture of mineralization.

Mineral Textures and Chemistry Trace the Origin and Transcrustal Evolution of the Sanyuangou Syenite in Southern North China Craton

Abstract Alkaline rocks are widely distributed in various geological environments and are important carriers for exploring the formation and compositional diversity of continental crust. Extensive studies have investigated the processes of mantle melting and crustal differentiation that produced such rocks. However, the potential interaction processes between mantle-derived magma and crust during their formation are poorly constrained. In this study, we focus on a Paleoproterozoic garnet-bearing syenite in the Xiong'er large igneous province (LIP) on the southern margin of the North China Craton through detailed whole-rock and mineral analyses. The high K2O (7.4–8.8 wt %) syenite emplaced at ~1772 Ma with ancient inherited zircon (1800–2800 Ma). The dominant mineral assemblage is composed of clinopyroxene, garnet, and K-feldspar with a small amount of titanite. Complex compositional oscillatory zoning of clinopyroxene and garnet indicates that magma mixing played a significant role in the formation of the syenite. We estimated the major elements composition for melts in equilibrium with clinopyroxene and calculated the clinopyroxene/melt partition coefficients by crystal lattice strain model, thus calculating the trace elements of the equilibrated melts. The equilibrium melts of high Mg# (>85) clinopyroxene have high CaO/Al2O3 (>0.6) and low Hf/Sm (<0.4), which suggests a role for carbonatitic metasomatism of the mantle. The variables La/Yb (24.4–56.1), Dy/Yb (0.8–5.9), and Yb (0.6–10.3 μg/g) indicate that the initial melts were formed by 1% to 2% partial melting of spinel-garnet phlogopite lherzolite. An REE-based model for melts in equilibrium with low Mg# (<85) clinopyroxene indicates that 10% to 30% felsic magma from ancient crust participated in hybridization. In addition to well-documented magma mixing, the oscillatory zoning of garnet is also related to competition with titanite. The initial alkaline magmas have a high water content (~4 wt %), which delays the crystallization of K-feldspar, leading to the enrichment of K2O, until the K-feldspar accumulates in the shallow crust to form the syenite. Magma mixing under an open system further leads to alkalinity enrichment. Magma source and crustal evolution jointly determine the potassium-rich characteristics of syenite. Multiple episodes of magma mixing and fractional crystallization occur in the crust (700–300 MPa), suggesting complex and vertically extensive magma chambers. This study represents the first identification of carbonatitic metasomatism as a mantle source in the Xiong'er LIP. Furthermore, it offers a new perspective on magma mixing between the mantle and crust in transcrustal magmatic systems, contributing to the formation of alkaline rocks.

The Impacts of Micro‐Porosity and Mineralogical Texture on Fractured Rock Alteration

AbstractGeochemically driven alterations of fractures in multi‐mineral media can create altered layers (ALs) at the fracture‐matrix interface. Spatial variations in the AL significantly influence mass transfer across the interface, and the hydraulic and mechanical properties of the fractured medium. A real‐rock based microfluidic experiment reported spatial variations in AL thickness despite the initially smooth fracture surface, suggesting potential effects of matrix heterogeneity on AL development. However, the respective contribution of structural and mineralogical characteristics is still poorly understood. Using the microfluidic experimental data and a micro‐continuum reactive transport model, we systematically evaluated how micro‐porosity and initial mineral texture impact AL development and thus the overall reactive transport behaviors. Our simulation results confirmed that the extent of AL spatial variations, mainly controlled by mineralogical texture, influences the evolution of reaction and permeability in different ways. Accounting for spatial heterogeneity in mineral distribution produces “channeling” structures in ALs and lower overall reaction (by up to 35.6%), but larger permeability increase (by up to 9.8%). The characteristic length of the reactive mineral cluster was observed to dominate the internal texture of ALs. Whereas the presence of micro‐porosity can enhance mineral accessibility via improving connectivity for flow and transport, and lead to both higher bulk reaction, that is, thicker ALs, and permeability enhancement. Considerations of surface roughness with characteristic length on the same order of magnitude as mineral texture did not change the overall development of AL, which further highlights the importance of accounting for rock matrix properties in predicting long‐term evolution of fractured media. The resulting spatial variations of ALs and their impacts on bulk properties, however, are expected to be further complicated by the coupling of chemical and mechanical processes, and may trigger matrix disaggregation, erosion and other mechanisms of fractured media alteration.

Petrological and geochemical insights into the magma plumbing system of the Daliuchong dacite eruption, Tengchong Volcanic Field, SW China

The formation of highly evolved, dacitic magmas has been attributed to various processes, including crystal fractionation, partial melting of overlying crust, and/or assimilation of crustal material into an evolving magma chamber. These processes are undoubtedly primary processes involved in the formation of dacites, but they may not be the only mechanism involved in the formation of high-silica dacites. For instance, mafic magma replenishment has been proposed as an additional mechanism but has not been assessed, and thus, its role has not been well-constrained. The Daliuchong volcano is the result of one of the largest eruptive events within the Tengchong Volcanic Field (TVF) in southwest China during the Early-Middle Pleistocene. Here, we conducted detailed mineral textures, mineral chemistry, and geochemical studies on Daliuchong pyroclastic rocks to explore the pre-eruptive storage conditions and evolution processes of the magma. The Daliuchong pyroclastic rocks are dacitic in composition. The samples show porphyritic textures characterized by phenocrysts of plagioclase, amphibole, clinopyroxene, orthopyroxene, and Fe-Ti oxides. Additionally, two distinct types of glomerocryst are identified: a gabbroic glomerocryst containing plagioclase + clinopyroxene + orthopyroxene ± Fe-Ti oxides assemblage and a dioritic glomerocryst containing plagioclase + amphibole ± pyroxene ± Fe-Ti oxides assemblage. Both phenocryst and glomerocryst show rich micro-textures. The Daliuchong dacite exhibits bulk compositional heterogeneity. Analysis of bulk-rock data suggests that this heterogeneity may arise from both the differentiation of the dacite itself and the injection of mafic magma. The compositional similarity between the Daliuchong dacite and experimentally produced partial melts of metamorphic basalt supports that the Daliuchong dacite was predominantly formed through the partial melting of the mafic lower crust. Thermobarometry estimation indicates that clinopyroxenes with high Mg# crystallized at 560–870 MPa, whereas amphibole and clinopyroxenes with low Mg# crystallized at 185–300 MPa. Based on the observed phase relations and the calculated crystallization conditions, we propose that during the differentiation of the Daliuchong dacite, heterogeneous dacitic magma formed by partial melting accumulated in a deep magma reservoir (21–32 km) before subsequently ascending toward shallower depths. Crystallization of plagioclase, amphibole, Fe-Ti oxides, and small amounts of pyroxene and apatite occurred at a shallower depth (7–10 km). The presence of coarse-sieve texture, fine-sieve texture, and oscillatory zoning with high amplitude in plagioclase suggests intermittent injection of mafic magma into the shallow magma reservoir, with the eruption of dacitic magma occurring after the final mafic magma replenishment. The petrological evidence above advocates that primitive magma replenishment could have been involved in the formation and triggered the eruption of dacite in the Daliuchong volcano.

To Mix or Not to Mix: Details of Magma Storage, Recharge, and Remobilization during the Pacheco Stage at Misti Volcano, Peru (≤21–2 ka)

Abstract We investigate ten of the most recent tephra-fall deposits emplaced between ≤21 and 2 ka from the Pacheco stage of Misti volcano, Peru, to elucidate magma dynamics and explosive eruption triggers related to magma storage, recharge, and remobilization. Whole-rock, glass, and mineral textures and compositions indicate the presence of broadly felsic, intermediate, and mafic magmas in a chemically and thermally stratified magma storage system (Zones 1–3) that interact to differing extents prior to eruption. Intermediate magmas are defined by plagioclase + amphibole + two-pyroxenes + Fe-Ti oxides and phase equilibria indicate they formed at ~300 to 600 MPa and ~950°C to 1000°C. Intermediate magmas dominate the Pacheco stage and either erupted alone as hybridized magmas or mingled with minor volumes of cool felsic magmas (~800°C) in which only plagioclase + Fe-Ti oxides are stable. Felsic magmas do not exclusively comprise any tephra-fall deposit emplaced during the Pacheco stage but were remobilized by recharge and mixing with intermediate magmas in order to erupt. Furthermore, felsic-hosted amphibole cognate to the intermediate magmas are reacted despite the felsic magmas being water saturated, which suggests they are staged above the amphibole stability limit (≤200 MPa). The cryptic presence of mafic magmas is indicated by high-An plagioclase cores (An74–88), rare anhedral olivine (Fo77–80), and possibly high Mg# augite and amphibole (up to Mg# 84 and 77, respectively). The dearth of basalt to basaltic andesite melts recorded in erupted glasses and exclusivity of high-An plagioclase to crystal cores signals mafic magmas are staged deeper in the crust than the intermediate magmas. Periodic interactions between these magmas tracked via glass compositions and crystal exchange reveal an alternation between the production of mingled magmas and their eruption shortly after a recharge event, followed by a period of homogenization and eruption of hybridized magmas. As such, we identify magma recharge as a key mechanism by which half of the explosive eruptions were triggered in the Pacheco stage. A >100°C increase in Misti’s fumarole temperatures from 1967 to 2018 coincident with changes in fumarolic gas compositions is consistent with degassing of a mafic recharge magma, signaling that Misti could produce similar explosive eruptions in the future.

Analysis of Microwave-Induced Damage in Granite Aggregates Influenced by Mineral Texture

The use of microwave energy to recycle high-quality coarse aggregates from waste concrete or assist hard rock breakage in underground building engineering is promising. Controlling or promoting the damage of coarse aggregates, i.e., hard rocks, under microwave irradiation is a crucial issue faced by these techniques. Understanding the damage mechanisms of hard rocks exposed to microwaves is thus urgent. Fracture toughness is a significant mechanical parameter of rocks that reflects their ability to resist crack propagation and damage evolution. In this study, the fracture toughness degradation of microwave-heated granite was investigated by combining experimental investigations and numerical simulations. A three-point-bending (TPB) experiment was conducted on granite specimens after microwave irradiation. A coupled electromagnetic–thermal–mechanical model considering the actual mineral texture of the granite specimen was established. The evolution of the temperature gradient and stress field near the initial notch tip were investigated. The results suggest that the microwave-induced maximum temperature gradient and stress in granite are at the plagioclase–quartz (Pl–Qtz) interfaces or inside the Pl near the boundary. The region of cracking initiation was defined as the damage zone, which could be obtained by comparing the microwave-induced thermal stress with the critical value. The fracture toughness degradation, which corresponds to the evolution of the damage zones, can be divided into two stages. A relatively rapid decrease in fracture toughness in the first stage is primarily caused by the spread of the scattered damage zones along the Pl–Qtz interfaces; subsequently, a gentler fracture toughness degradation results mainly from the extension of the previous damage zones.

The evolution of crystal‐poor rhyolite in the middle Okinawa Trough and its implications for the state of magma chamber

The crystal‐poor rhyolitic pumice is the product of extreme magma differentiation and is characterized by highly vesicular, honeycomb‐like structure. However, little is known about the evolutionary history and the time of volatile saturation of the pumice‐forming melt. A crystal‐poor rhyolitic pumice (TVG7‐1) has been collected from the Yoron Hole hydrothermal field in the middle Okinawa Trough, a young continental margin back‐arc basin in the western Pacific. This study conducted a detailed analysis on the texture and in situ chemical composition of plagioclase, orthopyroxene and Fe‐Ti oxides to reveal the evolution process, storage state and eruption triggers of eruptible silicic melt. Texture and zoning of specific minerals and mineral populations suggest a magmatic evolution history of open system. Additionally, the hollow reentrant texture, as well as results from plagioclase‐liquid hygrometers, confirm a water‐rich melt pocket. The exsolution of volatiles (H2O, etc.), in this melt pocket, will contribute to local oxidation conditions, which may have been recorded by the concordant behaviour of FeO and An in plagioclase. Then, the overpressure caused by volatile exsolution would destabilize the magma chamber, which will eventually be broken by magma mixing/recharge, and lead to violent melt evacuation. Consequently, crystal size distribution (CSD) provides a new perspective on understanding the kinetic effect of magma mixing/recharge in the Okinawa Trough, especially on the mineral populations. Our study reveals the petrogenesis of crystal‐poor rhyolite within the framework of the mush model, refines the magma evolution history and demonstrates that pumice magma reaches volatile saturation before the eruption.

Mechanical transport revealed by optical textures of heavy minerals in aeolian sand: A case study in the Badain Jaran Desert, Northwestern China

Determining whether and to what extent the relative abundance of heavy minerals in original detrital assemblage has been modified by mechanical transport is beneficial for understanding regional historical climate changes and acquiring modern sediment provenance information. Utilizing the frequency of surface mechanical optical textures of heavy minerals may be an effective approach to address this question. However, the connection between the frequency surface mechanical optical textures of heavy minerals and the variations in the relative abundance of these minerals remains uncertain. In this study, 12 modern aeolian sand samples were collected from the Badain Jaran Desert in hyper arid region of northwestern China, characterized by weak weathering to analyze their relative contents of five major heavy minerals. Then, 3796 transparent heavy mineral grains were photographed under the parallel light of a polarizing microscope, and the frequency of 13 surface mechanical optical textures were calculated. The results reveal that the variations in the relative abundance of heavy minerals are substantially influenced by mechanical transport. The decrease in the relative abundance of heavy minerals with weak mechanical stability primarily attributed to mechanical collision. Conversely, the variations in the relative abundance of heavy minerals with strong mechanical stability are primarily influenced by mechanical abrasion. Therefore, mechanical transport impact on the relative abundance of heavy minerals in regions with weak chemical weathering. Establishing heavy mineral characteristic indices for provenance studies using the relative abundance of mechanically unstable minerals may not directly indicate transport distance but rather the strength of wind forces, which have significant potential in palaeo wind regime studies. This study expands the research field of sediment surface micromorphology and has potential applications in inferring past climate changes and determining modern sediment provenance.

Computed Tomography of Scheelite Ore, Kara, Australia: Morphological Characterisation and Modal Mineralogy

Metal ores are mineralogically characterised to understand their genesis in order to allow informed decisions on mineral processing and to recognise likely environmental risks upon mining. However, standard mineralogical techniques generate only two-dimensional information at best, which in addition may be subject to sampling and stereological errors. By contrast, computed tomography (CT) is a non-destructive imaging technique that allows three-dimensional analysis of solid materials. In the present study, two ore types of the Kara Fe-W deposit (Australia) were characterised using CT to examine their mineral texture and modal mineralogy as well as scheelite distribution and ore grade (WO3). The results show that scheelite is primarily associated with hydrous phases (e.g., epidote, chlorite, amphibole) and occurs as massive or disseminated mineral as well as vein-fill at minor and trace concentrations. This study demonstrates that CT of scheelite ore enables accurate 3D texture visualisation (volume, grain size distribution) and yields valid quantitative data on modal mineralogy and WO3 grade of individual ore samples. Consequently, CT analysis of scheelite-bearing ore provides information relevant for ore genesis studies and comminution strategies for the possible recovery of scheelite as a by-product from metalliferous ores.

Re-distribution and upgrade of metals induced by the superimposition of later magmatic fluids in the Archean Hongtoushan VMS deposit, NE China

The Hongtoushan copper-zinc deposit is a highly metamorphosed Archean volcanogenic massive sulfide deposit (VMS) in China. After metamorphism, the deposit underwent later fluid superimposition, which is of significance for the re-distribution of metals and upgrading ores. However, the hydrothermal modification mechanism and fluid source remain unclear due to the difficulties in accurately recognizing the mineral textures and assemblages formed by hydrothermal modification. In this study, the mineral texture was investigated to identify the modification mechanism of later fluid and in situ sulfur isotope and trace elements of chalcopyrite were tested to track the source of later fluid and metals. The dominant assemblage formed by superimposed fluid consisted of pyrite, chalcopyrite, sphalerite, minor galena, magnetite, calcite, anhydrite, and hydrothermal alteration minerals, i.e. sericite and chlorite. These minerals infilled the fractures in early pyrite porphyroblasts or precipitated along the grain boundary. Additionally, the pre-existing sulfides were corroded by these minerals. They exhibited replacement and porous textures, indicating that the superimposed fluids resulted in a dissolution-reprecipitation process and formed new sulfides. The hydrothermal metasomatism produced the sericitization of plagioclase and chlorization of biotite, which concurrently liberated silica to form silicification. These interactions suggested that the hydrothermal fluid is acid fluid. The chlorite geothermometer defined the formation temperature of 226–279°C, implying that the superimposed fluid has a moderate temperature. The chalcopyrite precipitated from superimposed fluid either coexisted with pyrite (Ccp 2a) or magnetite (Ccp 2b). The sulfur isotope of Ccp 2a defined a closing zero range (0.75–2.41‰), demonstrating the superimposed fluids were derived from magmatic fluids. In contrast, the Ccp 2b enriched heavy sulfur with a δ34S range of 4.10–8.63‰, which was attributed to the oxidation of fluids. Partial ferrous ions were oxidized to ferric iron, and ferrous and ferric iron precipitated as magnetite. The mineral assemblage changed from chalcopyrite + pyrite, followed by magnetite + chalcopyrite + pyrite, to magnetite + pyrrhotite, representing the local increase of the oxidation state of hydrothermal systems. During the oxidation process, the oxygen fugacity of the superimposed fluid decreased, whereas the pH increased. These results provide crucial evidence on the re-distribution pattern of metals and the post-hydrothermal modification process in the Hongtoushan Cu-Zn deposit.

Mineralogical and chemical characterization of an oolitic iron ore, and sustainable phosphorus removal

An oolitic iron ore from Gara Djebilet, Algeria was characterized by X-ray diffraction, scanning electron microscopy, and energy dispersive spectrosopy and the phosphorus distribution between various phases studied. Two ore types were identified - a haematite-dominated, oolitic type and a more massive, magnetite-dominated type. The haematite-dominated ore had a higher phosphorus content, up to 0.6% in the iron oxide minerals, than the magnetite-dominated type (0.3% P). Owing to the very fine-grained texture of the gangue minerals, reducing the phosphorus content to levels suitable for steelmaking (below 0.05% P) by conventiobal means would entail an energy-intensive process with a high carbon footprint. Preliminary leaching test work using a sulphurous geothermal water as lixiviant, assisted by solar thermal acceleration, gave very promising results, removing 0.13% of the residual P (or 21.7% removal of total P) from the high-phosphorus oolitic ore.

Evaluation of sweet spots for a tight sandstone reservoir: A quantitative study of diagenesis in the fourth member of the Oligocene Huagang Formation, Xihu Depression, East China Sea Shelf Basin

Reservoir sweet spot evaluation is very important for tight sandstone gas exploration and development. Due to the characteristics of large burial depth, strong diagenesis heterogeneity, and prominent importance of diagenetic facies, sweet spot evaluation is the focus and difficulty of unconventional oil and gas exploration and development. By combining with core observation, conventional core analysis, clay x-ray diffraction analysis, bulk rock x-ray diffraction analysis, powder grain size analysis, thin section quantitative statistics, fluid inclusion homogenization temperature, scanning electron microscopy, scanning electron microscopy mineral quantitative evaluation, well logging data, and pre-stack seismic data, integrated simulation approach of seismic diagenetic facies and diagenetic numerical simulation was used to simulate porosity evolution and spatial distribution of tight sandstone of second submember (Smbr 42) of the fourth member (Mbr 4) of the Oligocene Huagang Formation in the Xihu Depression in the East China Sea Shelf Basin, and to evaluate reservoir sweet spot distribution. Based on mineral texture relationship and diagenetic sequence of Smbr 42 sandstone compaction, clay mineral transformation, calcite cementation, quartz cementation, and dissolution, five diagenetic facies were identified. Based on various seismic elastic parameters and core-derived diagenetic facies, the distribution of seismic diagenetic facies was interpreted by seismic diagenetic facies prediction method. Seismic diagenetic facies distribution can provide a “hard-constraint” three-dimensional diagenesis heterogeneity model for diagenetic history reconstruction, and seismic diagenetic facies distribution provides constraints on grain size and quartz grain content distribution in diagenetic numerical model. Based on the detailed consideration of input parameters of burial history, thermal history and diagenetic history, integrated diagenetic numerical simulation was used to reproduce porosity evolution and spatial distribution of Smbr 42 sandstone, and was applied to reservoir sweet spot evaluation of tight sandstone. Smbr 42-1 sublayer developed type III reservoir sweet spot and non-sweet spot. Smbr 42–2 to Smbr 42-6 sublayers mainly developed type II1, type II2, type III, and minor type I reservoir sweet spot. Simulation results were consistent with the locations of multiple sets of drilled gas layers and proven gas reservoirs.

Fluid-induced dissolution–reprecipitation of tungsten minerals in the Hongling deposit, South China

Tungsten is a critical metal that is predominantly found in magmatic-hydrothermal W-Sn deposits. However, the behavior and controlling factors of tungsten in highly evolved granitic systems are not yet well-known. In this study, we examined the integrated mineral textures and geochemistry of wolframite and scheelite from the Hongling tungsten deposit in the word-class Nanling W-Sn metallogenic belt, South China. Our results reveal that wolframite and scheelite from the muscovite granite of the highly evolved Reshui granite pluton can be classified into three generations formed through a process of coupled dissolution-reprecipitation. Wolframite with altered relict textures was formed during the early magmatic stage, while the two generations of scheelite (Sch-I and Sch-II) were formed during the magmatic-hydrothermal transitional stage. The formation of Sch-I, which exhibits a notable positive Eu anomaly, required the participation of external Ca-rich reduced fluids within the magmatic exsolved fluids from the highly evolved peraluminous pluton. The porous Sch-II occurs as marginal overgrowth or fracture-filling textures and exhibits a similar negative Eu anomaly as the dissolved wolframite. These three generations of tungsten minerals exhibit distinguishable REE contents and distribution patterns, with increasing LREE and decreasing HREE trends. The fluctuation of oxygen fugacity and the compositional evolution of tungsten minerals from wolframite through Sch-I to Sch-II indicate the involvement of external Ca-rich reduced fluids within the magmatic exsolved fluids from the highly evolved peraluminous pluton. The coupled dissolution of wolframite and the reprecipitation of scheelite were likely induced by intensive fluid-rock interactions, which are critical for the remobilization and enrichment of tungsten in magmatic-hydrothermal deposits. We inferred that such fluid-induced dissolution-reprecipitation of tungsten minerals provides new insights into the formation of the world-class Nanling W-Sn metallogenic belt in South China.

Impact of Chondrites on trace metal distribution in the sapropel S7 (ODP Site 966): Implications for paleoenvironmental and paleoceanographic reconstructions

Organic-rich deposits are valuable paleo-archives, recording significant paleoceanographic changes linked to past climate variations and marine deoxygenation events. The deposition of organic-rich sediments stops when bottom-water reventilation/oxygenation occurs. This impedes organic matter preservation, enabling macro and micro burrowing-organisms to recover and bioturbate the seafloor. In this sense, highly bioturbated sediments require particular attention when sampling is done for geochemical analyses, as sediments can be considerably mixed. While avoiding trace fossils during sampling for geochemical analyses is easy for large traces (e.g. Planolites, Thallasinoides, and Zoophycos), it becomes challenging for smaller and complex traces (< 0.5 cm), as is the case with Chondrites. Chondrites-producers have an opportunistic behavior, being one of the first organisms to colonize the seafloor after an anoxic event. As a result, Chondrites are commonly and sometimes abundantly found in the upper layers of organic-rich sediments, including sapropels and black shales.This study focuses on sapropel S7, which was deposited between ∼198.5 and 191.9 ka at the top of Eratosthenes Seamount and exhibits abundant Chondrites. For this sapropel, we demonstrated that Chondrites-producers can bioturbate significant volumes of organic-rich sediments (over 35%), introducing oxic/dysoxic material downward into anoxic sediments enriched in redox-sensitive trace metals and organic matter. This process can dilute up to 18% the original concentration of redox-sensitive trace metals (e.g. Mo, U and V). This dilution is especially important to consider when calculating trace metals and organic matter burial flux from bulk sediment data. Therefore, Chondrites-producers can play a crucial role in altering the sediment texture and distribution of minerals and organic matter at sub-cm scale, and may thus impact paleoenvironmental and paleoceanographic reconstructions based on geochemical signals. Furthermore, the subsequent redistribution of organic matter and redox-sensitive trace metals (including oligoelements) within the sediment can affect carbon and nutrient cycling, microbial activity, organic matter degradation in deep-marine sediments, and the overall sedimentary biogeochemistry.