Search Results (190)

The magmatic Ni-Co-Cu mineralization in the Iken deposit in the central part of the Kun-Manie complex, Amur Oblast, Russia, hosted by an olivine-bearing websterite, is of a low-sulfide type. The fine-grained disseminations of base metal sulfides (BMS), dominantly pyrrhotite, pentlandite (a major source of Ni of industrial importance), and chalcopyrite, are followed by a scarce Pd-Pt-Ag mineralization. Elevated contents of Al in orthopyroxene (mean 2.78 wt.% Al₂O₃) along with Al–Na enrichment in clinopyroxene (diopside; mean 5.10 wt.% Al₂O₃) are associated with highly aluminous compositions of low-chromium members of the spinel–hercynite series. High levels of TiO₂ in kaersutite and titanian phlogopite also reflect a pronounced degree of fractionation of the ore-forming melt. Minor portions of sulfide melt are distributed evenly as a result of immiscibility at advanced stages of orthopyroxene crystallization, after the formation of olivine. Differentiated grains of droplet-like BMS largely settled in situ close to grain boundaries of orthopyroxene or occupied interstitial spaces of pyroxenes and olivine in association with spinel–hercynite and fluorapatite. A combination of late saturation in S with relatively quick cooling rates of the hypabyssal body prevented the effective settlement and accumulation of sulfide droplets in the ore zone. The well-developed lamellae of troilite (Fe₅₀S₅₀) exsolved from the host pyrrhotite Fe₄₈S₅₂ during subsolidus cooling, as a consequence of a low-temperature reaction triggered by a sudden drop in fO₂. An influx of mantle-derived fluid bearing CO₂, CO, and CH₄ with the rising magma could be the primary cause of the fO₂ reduction. Also, graphite-bearing metasedimentary rocks could have been assimilated. Tiny grains of minerals of noble metals (moncheite and merenskyite with essential amounts of melonite component, sperrylite, hessite, alloy Au_63.2Ag_36.8, and argentopentlandite) deposited late in a fluid-enriched medium under submagmatic conditions. Full article

Volcanic rocks of the Qi’eshan Group, which are widely distributed in the Dananhu arc of the Eastern Tianshan, NW China, have long been debated in terms of their formation age and tectonic setting. In this study, we conducted an integrated study of U-Pb apatite geochronology, whole-rock major and trace element geochemistry, in situ major element analyses of clinopyroxene, and “Rhyolite-MELTS” thermodynamic modeling on the basalts from the Qi’eshan Group. Geochronological data show that the weighted mean of ²⁰⁶Pb/²³⁸U ages of apatite is 329 ± 10 Ma. The basalts belong to the tholeiitic series and are characterized by enrichment in large ion lithophile elements (LILEs), depletion in high field strength elements (HFSEs), and enrichment of light rare earth elements (LREEs) relative to heavy rare earth elements (HREEs) with weak negative Eu anomalies. They were derived by partial melting of garnet-spinel lherzolite in a depleted mantle source metasomatized by subduction-related fluids, followed by fractional crystallization of spinel, olivine, and clinopyroxene. Clinopyroxene is dominated by augite, characterized by high Mg and Ca contents and low Al and Na contents. Machine-learning-based thermobarometry indicates that clinopyroxene crystallized at temperatures of 1027–1033 °C and pressures of 1.1–1.6 kbar. “Rhyolite-MELTS” isobaric crystallization simulations suggest that mantle-derived magma, with an initial water content of 4 wt.% and oxygen fugacity of FMQ, can generate melts compositionally similar to the volcanic rocks of the Qi’eshan Group through fractional crystallization at a pressure of 1.5 kbar. Combined with previous studies, we propose that the Qi’eshan Group basalts formed in an extensional arc setting related to southward rollback of the northward-subducting Kanguer oceanic slab, which caused asthenosphere upwelling and lithospheric extension, thereby promoting partial melting of the subduction-metasomatized mantle. Our data provide new insights into the Carboniferous rollback of the Kanguer oceanic slab in the northern part of the Eastern Tianshan. Full article

The Heilongtai–Maogudui (HM) mafic intrusions are exposed in the southern margin of the North China Craton (SNCC), which are contemporaneous with a variety of strategic metal/non-metal minerals (niobium, uranium, and high-purity quartz) and magmatic hydrothermal REE deposits. New geochronology and geochemistry of these intrusions are examined and interpreted to decipher their petrogenesis and tectonic settings. Zircon LA–ICP–MS data formed a concordant cluster, yielding a mean ²⁰⁶Pb/²³⁸U age of 397.5 ± 3.5 Ma, which is interpreted as an Early Devonian crystallization age. The HM mafic intrusions have similar whole-rock geochemical compositions, containing 48.94–51.51 wt% SiO₂, 1.26–1.61 wt% TiO₂, 5.96–7.13 wt% MgO, and 11.00–12.48 wt% FeO_t. The total alkali contents range from 1.61 wt% to 3.53 wt%, with Mg^# values of 47.23–52.30. The petrographic and geochemical results suggest the fractional crystallization of mainly olivine, clinopyroxene, and minor Fe–Ti oxide in the mafic intrusions. Being of tholeiitic composition, these mafic rocks display relatively flat rare earth element (REE) and trace element patterns, which are similar to those of the normal mid-ocean ridge basalt (N–MORB) and the enriched mid-ocean ridge basalt (E–MORB). The HM mafic intrusions are proposed to originate in the continental extensional environment through 5–10% partial melting of the depleted spinel asthenosphere mantle source. This is attributed to the gravitational delamination of the lithospheric mantle and the upwelling of the hot asthenosphere, marking the end of the Paleozoic Proto–Tethyan orogenic cycle. The Paleozoic strategic mineral deposits are proposed to have formed under this specific tectonic regime. Full article

This paper presents systematic petrological, whole-rock geochemical, and Sr-Nd-Pb isotopic studies on the mafic–ultramafic rocks of the Daaobaogou Ni-Cu sulfide deposit in the Dunhuang Block, Gansu Province. This study aims to reveal the nature of its source region, parent magma composition, and magma evolution processes. The results indicate that the parent magma of the ore-bearing intrusion in Daaobaogou originated from an enriched lithospheric mantle metasomatized by Paleozoic subduction processes. It exhibits high-magnesium characteristics and represents the product of a certain degree of evolution from a primitive magma. The magma evolution underwent significant fractional crystallization, with olivine beginning to crystallize at 1328 °C, following the crystallization sequence: olivine, clinopyroxene, plagioclase, and orthopyroxene. Sr-Nd-Pb isotopes and trace elements indicate that the magma experienced intense crustal contamination (approximately 10–20% upper crust) during its ascent. Full article

Mafic ultrapotassic volcanics (kamafugites, mafurites) are the youngest eruptives in the Bunyaruguru volcanic field, which is part of the Toro Ankole Province at the northernmost reach of the West Branch of the East African Rift Valley. We obtained new data using LA-ICP-MS on the trace element contents (rare earth, large ion lithophile, high field strength and compatible elements) in clinopyroxene phenocrysts from mafurite lava of the Bunyaruguru volcanic field. The clinopyroxenes are notable for their anomalously high zirconium contents (up to 800–1000 ppm), which is unusual in mafic silicate magmas but typical for clinopyroxenes from carbonatite lavas. This distinctive signature is not found in clinopyroxene in coeval mafic lavas from neighboring vents. Carbonate is also found in the Bunyaruguru volcanic rocks in the form of inclusions in high-Mg olivine phenocrysts, suggesting carbonated material exists in the source of kamafugite magmas. Carbonatites are widespread in the neighboring Fort Portal volcanic field, and we interpret the high-zirconium clinopyroxene as evidence for mixing of mafurite magmas with carbonatite melts. Full article

The Abrolhos Magmatic Province (AMP), situated along the southeastern Brazilian passive margin, comprises a Paleocene–Eocene transitional basalt series of alkaline affinity. Despite the lack of mineral chemistry and thermobarometric estimates, it has long been linked to a classical deep-mantle plume model. This study integrates mineral chemistry, calculations of intensive parameters (P, T, H₂O), geochronology, and geochemical modeling to evaluate an alternative explanation for AMP magmatism. Whole-rock and clinopyroxene compositions from different AMP localities are consistent with parental magmas derived from fertile, pyroxenite-enriched mantle sources that melted under ambient mantle potential temperatures (~1300–1400 °C). Inverse petrological modeling using alphaMELTS and MeltPT, together with trace-element systematics, suggests low degrees of partial melting within asthenospheric domains. These results indicate that shallow (upper-mantle) processes and high mantle fertility were important controls on melt generation. New ⁴⁰Ar/³⁹Ar ages of 24.3–28.4 Ma for southern AMP rocks are also difficult to reconcile with a simple age-progressive evolution of the previously proposed plume model. Taken together, the data support ambient-temperature melting of a fertile mantle as a plausible explanation for Abrolhos magmatism and reduce the need to invoke a classical high-temperature mantle plume as the sole model. Here, we favor a tectonically controlled model, involving localized shallow mantle processes such as edge-driven convection and/or lithospheric delamination as triggers for intraplate magmatism along the South Atlantic margins. Full article

Diopside–hedenbergite solid solution is the most common clinopyroxene end-member combination in mafic and ultramafic igneous rocks. The crystal structure variety caused by Mg-Fe isomorphous substitution can indicate geological processes such as Mg-Fe isotope fractionation. To explore the effect of Hubbard U correction and Fe content on iron-bearing clinopyroxene structures, we employed GGA and GGA + U to study the lattice constants, unit-cell volume, and average Fe-O bond length of the diopside–hedenbergite solid solution series. On the whole, the results by GGA + U are the increase in lattice constant a (from 9.910 Å to 10.030 Å) and volume (from 456.656 ų to 464.640 ų), the decrease in β angle (from 106.121°to 105.320°), and a slight variation in the lattice constant b (from 9.007 Å to 9.010 Å) with increasing Fe content, which is a better match with the experiment than those by GGA. The average Fe-O bond lengths and polyhedral volumes calculated by GGA and GGA + U both increase with increasing Fe content. The Hubbard U correction significantly affects the lattice constants and unite-cell volume at medium-high Fe content (Fe/(Ca+ Mg + Fe) > 2/8), the Fe-O bond at low Fe content (Fe/(Ca+ Mg + Fe) < 1/8), the bond angle variance, distortion index and quadratic elongation at relatively medium Fe content (1/8 ≤ Fe/(Ca+ Mg + Fe) ≤ 5/16). This study verifies the effectiveness of U-value correction on iron-bearing clinopyroxene and provides a theoretical basis for understanding its structural evolution. Full article

Interstitial microstructures in igneous rocks record key evidence of late-stage evolution processes. In order to constrain the late-stage evolution of a Baima gabbro pegmatite (Panxi region, SW (Southwestern Sichuan Province), China), we investigated its mineral compositions and late-stage microstructures. These microstructures include replacive symplectites and fish-hook clinopyroxene. Replacive symplectites include fine-grained lamellar intergrowths of anorthite (An)-rich plagioclase + clinopyroxene/amphibole/biotite that are rooted to Fe-Ti oxides and replacing nearby plagioclase primocrysts (Type I) and intergrowths of An-rich plagioclase + clinopyroxene/amphibole that are rooted to olivine and replacing nearby plagioclase primocrysts (Type II). Rare replacive symplectites composed of biotite + plagioclase are also present. Those replacive symplectites and fish-hook clinopyroxene grew at a late magmatic stage with temperatures of 867–1023 °C. An-rich plagioclase in the replacive symplectites and fish-hook textures have An contents up to 94 mol.%, much higher than those of plagioclase primocrysts. Interstitial microstructures are interpreted to reflect interaction between primocrysts and an Fe-rich residual interstitial liquid, consistent with separation and migration of conjugate immiscible melts in a crystal mush. We propose that the hydrous interstitial melt in the Baima gabbro pegmatite may have undergone silicate immiscibility during late-stage magma crystallization. As the crystal fraction increased, crystal-mush compaction and porous melt migration likely became the primary controls on the evolution of the late-stage interstitial melt, rather than convection or diffusion. Full article

To understand the dislocation creep behavior of water-saturated clinopyroxene in the upper mantle, we conducted high-temperature triaxial compression experiments on hot-pressed diopside aggregates under water-saturated conditions at confining pressures of ~300 MPa and temperatures of 1373–1473 K using a Paterson gas-medium apparatus. Fourier transform infrared measurements of the water contents revealed that all experiments were performed under water-saturated conditions. Fitting the mechanical data with a power flow law yielded a stress exponent n of 2.2 ± 0.6, an activation energy Q of 442 ± 33 kJ/mol, and a material-dependent parameter A of 10^6.9±0.5 MPa^−2.2 s⁻¹. For comparison, a single deformation experiment was performed under anhydrous conditions at a temperature of 1473K. The mechanical results show that the water-saturated diopside aggregates deform approximately 1.5–3 orders of magnitude faster than their anhydrous counterpart, indicating a pronounced water-weakening effect. Furthermore, under water-saturated conditions, our mantle-derived diopside aggregates have comparable strengths to that of Fe-rich Sleaford Bay clinopyroxene at 1473 K and laboratory strain rates but significantly weaker than that of olivine aggregates. The results in this study provide key experimental constraints on the flow behavior of mantle-derived clinopyroxene aggregates under water-saturated conditions. Full article

The Wailukum area in North Maluku Province, Indonesia, is an ultramafic rock complex with a high degree of serpentinization. The mineral composition of ultramafic and mafic rocks strongly influences the distribution and enrichment of scandium (Sc) during lateritization. In this study, we aim to analyze three types of geological materials in a lateritic profile that contains Sc, specifically bedrock, saprolite, and limonite, in terms of element distribution, mineral composition, and rock identification. We used the analytical methods of petrography, X-ray diffraction (XRD), X-Ray Fluorescence (XRF), and Inductively Coupled Plasma–Optical Emission Spectroscopy (ICP-OES). The results show that Sc in bedrock is mainly associated with clinopyroxene minerals such as augite and diopside. In saprolite, Sc content decreases due to higher mobility but remains partly associated with clinopyroxene, and in limonite zone, Sc reaches maximum enrichment. Among rock types, gabbro contains the highest absolute Sc concentration (23.25 ppm in bedrock and up to 58.5 ppm in limonite), while wehrlite records the greatest enrichment ratio, with a 9.18-fold increase from bedrock to limonite. By contrast, gabbro shows the lowest enrichment ratio (2.52-fold) despite its high initial Sc content. These patterns indicate that Sc enrichment is controlled by clinopyroxene as the primary host in bedrock, affecting its relative stability during weathering. Full article

To investigate the influence of a second-phase mineral on the rheology of mantle peridotite, we conducted high-temperature deformation experiments on dry olivine–clinopyroxene (Ol-Cpx) aggregates. Cylindrical samples were manufactured using hot-isostatic pressing techniques, with Ol as the matrix phase and Cpx added at volume fractions of f_Cpx = 0.1, 0.3, and 0.5. Deformation experiments were performed in a Paterson gas-medium apparatus at a confining pressure of ~300 MPa, temperatures ranging from 1423 to 1523 K, and strain rates of ~5 × 10⁻⁶ s⁻¹, ~1 × 10⁻⁵ s⁻¹, ~2 × 10⁻⁵ s⁻¹, and ~5 × 10⁻⁵ s⁻¹. The stress exponents (n = 3.4–4.3) for two-phase aggregates are comparable to those reported for both pure Ol and pure Cpx, indicating that dislocation creep remains the dominant deformation mechanism. Increasing Cpx content does not induce a transition of dominant mechanism but leads to a slight decrease in activation energy, consistent with predictions from two-phase rheological models and reflecting the increasing contribution of Cpx to bulk deformation. Normalized flow stresses fall between the Ol and Cpx end-members within the Taylor–Sachs bounds, indicating moderate strain partitioning between phases. Aggregates with f_Cpx = 0.5 show slightly reduced strength and lower effective stress exponents. This is attributed to enhanced dynamic recrystallization, which triggers grain-size reduction and thereby increases the contribution of diffusion-assisted deformation, even though dislocation creep remains the dominant mechanism. These results suggest that under dry conditions, Cpx primarily modulates the rheology of olivine-rich aggregates through microstructural evolution and strain partitioning rather than by altering the dominant deformation mechanism. Full article

Dependence on fertilizers limits the sustainability of tropical agriculture. Remineralization using rock byproducts offers a solution that is conditioned by the mineralogical–soil interaction. This study evaluated the agronomic and geochemical potential of a gabbro rock byproduct (GRB) as a bulk amendment in yellow maize (Zea mays L.) cultivation in Atlántico, Colombia. The specific objectives were (1) to characterize the mineralogy and geochemistry of the local GRB; (2) to quantify its neutralizing and fertilizing effect in an acidic Arenosol soil; and (3) to evaluate the biometric response of yellow maize (Zea mays L.) in a field trial. The trial was conducted in an acidic haplic Arenosol (pH 5.4) in 2023, with a 70-day cycle, comparing three management systems: M1 (control), M2 (47 Mg·ha⁻¹ GRB, seed type: ICA-109), and M3 (47 Mg·ha⁻¹ GRB, seed type: V-114). The assessed GRB, with 52.75% SiO₂ and 5.46% CaO, is rich in calcic plagioclase, clinopyroxenes, and zeolites. Application of GRB at 47 Mg·ha⁻¹ in treatment M3 coincided with marked changes in soil properties over the course of the trial, with pH rising from 5.4 to 6.4, cation exchange capacity from 5.0 to 12.1 cmol_c·kg⁻¹, and available phosphorus from 9.8 to 35.0 mg·kg⁻¹. Plants in M3 showed statistically significant increases (p < 0.001) in ear weight (median: 150 g vs. 60.5 g in M1) and in vegetative development. Because the trial was pseudo-replicated, used a high single-dose “shock-loading” rate, involved different maize genotypes across treatments, and covered only one 70-day cycle, these results should be interpreted as exploratory and site-specific. Even so, they indicate that GRB can act as an effective acidity corrector and slow-release multinutrient source under Arenosol conditions, with relevance for circular-economy strategies. Future work should evaluate agronomically doses, include replicated multi-cycle trials, and incorporate comparative and risk-assessment analyses. Full article

Mylonitic mantle peridotites exposed at the Tosa Megamullion in the Shikoku Basin, Philippine Sea, provide direct evidence for amagmatic ductile shear deformation of the upper mantle beneath a back-arc spreading center. Oceanic core complexes (OCCs), or megamullions, are dome-shaped structures formed by detachment faulting and occur locally along slow-spreading mid-ocean ridges and back-arc basins, where they expose fault rocks derived from ductile shear zones in the lower crust and upper mantle. The Shikoku Basin hosts several OCCs, including the Tosa Megamullion, which formed during the early stage of back-arc spreading. In this study, nine ultramafic rocks were collected from the Tosa Megamullion using the submersible Shinkai6500 during cruise YK23-05S. Although all samples were highly serpentinized, several preserved primary peridotitic textures were composed mainly of olivine, orthopyroxene, with subordinate clinopyroxene, plagioclase, and spinel. Seven samples exhibit well-developed foliation and porphyroclastic textures dominated by orthopyroxene porphyroclasts, ranging from rounded to strongly elongated forms, commonly showing microkinks and undulose extinction. Crystallographic preferred orientations (CPOs) of three representative samples, analyzed using SEM-EBSD, reveal E-type-dominant olivine fabrics characterized by the (001)[100] slip system, with a subordinate contribution from C-type (100)[001] slip. These CPOs suggest deformation under non-dry conditions involving moderate hydration and/or elevated differential stress. These results indicate that the ultramafic rocks from the Tosa Megamullion represent mantle-derived mylonitic peridotites formed by ductile shear beneath the spreading axis and subsequently exhumed under strongly magma-poor, amagmatic conditions. The Tosa Megamullion thus represents an amagmatic end-member of the OCC formation in back-arc basins, dominated by tectonic strain localization rather than by magmatic accretion. Full article

The observed shortage of water resources in the western and southern regions of the Russian Federation may soon affect the territory of the Republic of Bashkortostan. An increase in the share of groundwaters can help to solve this problem. To provide the population of the republic with water resources, the groundwater of magnesium–bicarbonate-type from the Kraka ophiolite massifs can be used. The massifs occur on the western slope of the Southers Urals. In this work we studied ultramafic rocks and their influence on the formation of the chemical composition of water. The research area is located in the northern part of the Zilair synclinorium, which occurs within the Central Ural megazone. In terms of hydrogeology, of particular importance to the territory of the synclinorium is the Zilair basin of fracture waters of the second order, which is part of the Uralian hydrogeologic folded zone. The ultramafic rocks from the studied area have consistently high CaO/Al₂O₃ ratios (0.4–1.6), which indicates the widespread development of parageneses with participation of clinopyroxene and a low degree of depletion of the primitive mantle source. Because of the complex geological structure of the area, water samples collected from both water points in the Kraka massifs, and the surrounding Early–Middle Paleozoic rocks were analyzed for major ions using a laboratory method to identify possible hydro-geochemical zoning. A statistical analysis was then conducted based on the obtained anion–cation composition data. From the viewpoint of the hydrolytic concept, the formation of the chemical composition of groundwater takes place due to the removal of Mg²⁺ from the rock-forming minerals of ultramafic rocks (olivine and pyroxene) and the supply of Na⁺, K⁺, Ca²⁺, and SO₄²⁻ Cl⁻ from atmospheric precipitations. The bicarbonate anion has a complex nature, where both biochemical processes in the soil and atmospheric precipitation play a significant role. Magnesium–bicarbonate-type of waters, due to low mineralization (to 1 g/L) and the majority of other geochemical parameters (pH of the medium, and content of Na, K, Ca, SO₄, and Cl), whose values that are within the limits set by the World Health Organization (WHO), can be used as drinking water. The increased values of total hardness (0.20–3.39 mmol/L) in accordance with the regulatory document SanPiN 1.2.3685–21, adopted by the Russian Federation, do not exceed the maximum permissible concentrations (up to 7.00 (10.00) mEq/L or 3.50 (5.00) mmol/L). The high magnesium content, in accordance with GOST (state standard) R 54316–2020, allows the magnesium–bicarbonate waters of the Kraka massifs to be classified as table mineral waters for the treatment of various diseases (including hypomagnesemia). Full article

Samples of flotation tailings generated during the exploitation and processing of Zn–Pb–Cu–Ag ore from the Rudnik mine (Serbia) were investigated for their mineralogical, geochemical, and magnetic susceptibility properties. The flotation tailings consist of a complex mineral assemblage, including silicates, carbonates, sulfides, phosphates, sulfates, oxides, hydroxides, and native elements. Quartz, calcite, and orthoclase dominate the coarse fraction (>400 µm), accompanied by epidote, Ca-garnet, and Ca-clinopyroxene. Sulfide minerals are concentrated in finer fractions (<400 µm), with pyrite and arsenopyrite being the most abundant, followed by pyrrhotite, sphalerite, galena, and chalcopyrite. These sulfides occur as dispersed grains within a silicate–carbonate matrix. Post-depositional oxidative alteration is moderately developed, with pyrite replaced by hematite, galena by cerussite, and chalcopyrite by malachite. Geochemical analyses reveal that SiO₂ (avg. 38.98 wt%), Fe₂O₃ (avg. 23.68 wt%), Al₂O₃ (avg. 8.95 wt%), CaO (avg. 9.03 wt%) and MgO (avg. 1.50 wt%) dominate the composition. Economically significant metals include Zn (avg. 0.47 wt%), Pb (avg. 0.20 wt%), Cu (avg. 0.11 wt%), Ag (max. 19 µg/g), and Bi (max. 130 µg/g). Mass magnetic susceptibility shows a strong correlation with S (r = 0.92), Co (r = 0.90), and Bi (r = 0.87); moderate correlation with Fe₂O₃, Al₂O₃, and As; and negative correlation with Mn, TiO₂, Zn, and Pb. The ferromagnetic phase most likely originates from pyrrhotite, as well as hematite formed during pyrite alteration and goethite. Full article