Mineral Chemical Analyses Research Articles

Mapping hydrothermal alteration in regolith using white micas and chlorite as vectors towards gold mineralization

Mineral exploration through regolith-dominated terrains poses a significant challenge to cost-effective exploration techniques. Due to missing surface expression, undercover mineral exploration relies on understanding ore-forming processes and characterizing alteration regimes to decipher suitable vectors towards ore deposits. The work presented focuses on the Archean granite-greenstones of the Yilgarn Craton, east of the Meekatharra area in Western Australia, and characterizes the weathering profiles by understanding metal dispersion mechanisms and identifying mineralogical vectors towards gold mineralization within regolith. Mineral mapping of gold mineralization using TESCAN Integrated Mineral Analyzer and laser ablation ICP-MS shows gold is associated with multiple generations of pyrite, and base metal sulfides and sulfosalts hosted in felsic to intermediate volcanics and volcaniclastics. Intensive weathering generated a thick regolith profile dominated by a leached zone of kaolinitic and micaceous saprolite underlain by a supergene Au-Cu deposit blanket at the base. The supergene deposit is dominated by colloform and framboidal pyrite, with pure microcrystalline Au, chalcocite, bornite, malachite, and alunite. Hyperspectral analyses were used to trace the composition and abundance of chlorite and white mica variations in the host rock and the weathering profile. The mineral assemblage in the hydrothermal alteration halo proximal to and intersecting gold mineralization is dominated by Fe-rich chlorite and Na-rich white mica (paragonite). Fe-rich chlorite and paragonite are spatially tied to elevated Au concentration and trends to Fe-Mg-rich chlorite and K-rich white mica (muscovite) distal to the alteration. The variations in chlorite chemistry were detected mainly in bedrock and saprock. Conversely, the white mica chemistry variations were detected in bedrock and the regolith profile, in which white micas resist intensive weathering. The spectral signatures identified through short-wave and thermal infrared data are verified through X-ray diffraction, mineral chemistry, and bulk geochemical analyses. This distinctive spectral signature of white mica and chlorite is a cost-effective exploration method for regional mapping of mineral systems to identify hydrothermal alteration footprints in the regolith developed over felsic and intermediate rocks.

The composite metamorphic sequence in the Jiajika gneiss dome, Songpan-Ganze orogenic belt, eastern Tibet: P-T-D-t evolution and implications for lithium mineralization

The metamorphic host rocks of pegmatites can help to decipher their geodynamic setting and emplacement conditions. The Jiajika lithium deposit, located in the Songpan-Ganze orogenic belt, eastern Tibet, is one of the largest hard-rock type lithium deposits in China. The lithium-enriched pegmatites in Jiajika are hosted in the amphibolite facies metasedimentary rocks in the mantle of the Jiajika gneiss dome. However, the metamorphic evolution of Jiajika is poorly constrained. In this study, we carried out detailed fieldwork, petrological observation, mineral chemical analysis, phase equilibria modeling, and geochronological studies on the Jiajika gneiss dome and the borehole JSD-1 (with a total depth of 3211 m) of the Jiajika Scientific Drilling Project (JSD). Structural data outlined two subdomes within the Jiajika gneiss dome. Two main stages of regional metamorphism and deformation are documented in Jiajika: an early Barrovian metamorphism (M1) in ca. 237−221 Ma caused by crustal thickening (D1), which has a peak condition of 6.7−8.3 kbar and 649−694 °C; a late Buchan metamorphism (M2) induced by the emplacement of granites and pegmatites during doming (D2) with a peak condition of 3.4−4.3 kbar and 570−612 °C at 210−206 Ma. The superimposition of the M2 isograds upon the M1 isograds resulted in a composite metamorphic sequence around the Jiajika gneiss dome. The overlapping of the Barrovian metamorphism and the Buchan metamorphism is related to crustal thickening during continental collision and later decompression through doming, which facilitated lithium mineralization.

Mineral chemistry and geothermobarometry of metasedimentary rocks of Central Menderes Massif, Western Türkiye: Metamorphic evolution and source of metapelitic rocks

The Menderes Massif (MM) is the largest metamorphic massif of Türkiye. This study was carried out to determine the origins, metamorphic conditions and age of garnet-mica schists covering large areas in the Central Menderes Massif (CMM). Detrital zircon dating of a garnet-mica schist derived from a quartzofeldspathic source measured the youngest zircon age to be 450 ± 61 Ma (102 % concordant, Th/U = 0.02) Ma and the oldest zircon age to be 1529 ± 18 Ma (97 % concordant, Th/U = 0.02) Ma. The ƐHf(t) values of the selected zircon grains vary between −27.42 and −3.43, and the 176Lu/177Hf isotope values vary between 0.2820 and 0.2827, and these values are consistent with the values obtained from the orthogneisses and paragneisses of the massif. The presence of five Ordovician zircon grains in garnet-mica schists and the intrusive contact with Triassic granites indicate that the source rock of the schists may have been deposited in the Late Ordovician - Triassic interval. Mineral chemical analyses show that garnets are almandine, biotites are Fe-biotite and white micas are muscovite-phengite in composition, and they are affected by metamorphism (greenschist - lower amphibolite facies) under ∼5 kbar pressure and ∼600 °C temperature conditions. For the first time, rutile UPb dating shows that garnet-mica schists underwent metamorphism 43.1 ± 6.1 Ma ago. PT conditions and metamorphic ages obtained from garnet-mica schists show that the overlying units underwent metamorphism in the greenschist-lower amphibolite facies in the Lutetian (Eocene) period.

Structural evolution and exhumation events recorded in the Huingancó Granodiorite, Cordillera del Viento, Southern Central Andes, Argentina

This study seeks to unravel the exhumation history of Permian granodiorites corresponding to the Huingancó volcano-plutonic Complex in the southern sector of the Cordillera del Viento (∼37°S), located within the Chos Malal fold-thrust belt. In this context, mineral chemistry analyses were conducted on the granodiorites using electron microprobe data to infer the P-T conditions of emplacement, resulting in 700–900 °C and pressures ranging between 1 and 2.4 kbar. Employing a geostatic gradient of 3.7 km/kbar, these values give an estimate of emplacement depths between 4 and 9 km. In order to understand their exhumation path, five samples from the Huingancó Granodiorite were taken along the Huaraco creek on the western flank of the Cordillera del Viento anticline to perform apatite fission track (AFT) analysis. This analysis yielded new cooling ages for the study area ranging between 50 and 80 Ma. Furthermore, inverse thermal modeling using the fission track data revealed two significant exhumation events during the Andean cycle: one during the Late Cretaceous-Paleocene and the other in Miocene times, separated by a period of gradual cooling or stability during Eocene-Oligocene times. These important cooling events are associated with the main construction phases of the Cordillera del Viento. Finally, to characterize its deformation evolution, a structural kinematic model is proposed based on a balanced structural section and its reconstruction to its non-deformed pre-Cretaceous state. The resulting model allows us to identify the structures and mechanisms of uplift rising the Cordillera del Viento, and their association with the main exhumation events depicted in the inverse thermal modeling. The main structure of the Cordillera del Viento corresponds to a fault bending fold that involves the basement in the deformation. Subsequently, its insertion as an intracutaneous wedge is related with the development of the thin-skinned structures at the internal sector of the Chos Malal fold and thrust belt.

Geochemical and geochronological evidences from Cambrian to Ordovician protracted magmatism in the Istranca Massif, NW Türkiye

Plutonic rocks in different ages are cropted out and form the basement rocks in the Istranca Massif. One of the plutons located at the basement is the Cambrian-Ordovician Vize pluton (Vize-Kırklareli) and is distinguished from other plutons by some of its characteristic features. This pluton intruded into the high-grade metamorphic sedimentary rocks, and is unconformably overlay by Triassic low-grade metamorphic rocks and Eocene aged coral reef limestones (Soğucak Formation). Based on new whole rock geochemical and zircon UPb data concentrated in two different ages, it can be said that the Vize pluton was affected by protracted magmatic activity. The igneous minerals and texture of Vize pluton are partly preserved, It has a mylonitic texture, a distinct foliation consisting of light and dark zones. In addition, metagranites contain mafic magmatic enclaves (MMEs) in some places.The Vize pluton is an I-type pluton with predominantly peraluminous and slightly metaluminous character. It is also High-K, calc-alkaline, and reflecting volcanic arc and post-collisional tectonic settings. Mineral chemical analyses show that the mafic minerals in the Vize pluton consist of Fe-biotite and calcic amphibole (hornblende). Ti-in biotite thermometry shows that the temperature of the pluton in the final crystallization temperatures are between 834 and 850 °C (mean = 845 ± 4 °C), while the crystallization temperatures of amphiboles are between 876 and 910 °C (mean = 893 ± 22 °C). Crystallization depths are estimated to be a range of 6.5 to 7.9 km. It can be assumed that the oxygen fugacity of calcic amphiboles (logƒO2) is stabilized between −10.7 and − 11.3 bar (mean = −11.05 ± 0.4 bar). ∆NNO values are between 0.72 and 1.11 (mean = 0.96 ± 0.12) and H2O melt content is between 4.63 % and 5.43 % (mean = 5.04 ± 0.4 %). Oxygen fugacity values are among the typical values of calc-alkaline magma crystallization.The Vize pluton was crystallized in Cambrian to Ordovician times according to zircon UPb dating is concentrated in two different populations as 526.16 ± 3.26 Ma and 452.93 ± 2.76 Ma. All data obtained are consistent with the ages of the magmatism that produced the Vize Pluton in the Balkanides and Istranca Massif of 420–470 Ma (mean 447.17 ± 3.24 Ma) and indicate that it probably formed in the northern Gondwana. It was affected by the magma-mixing processes of coeval felsic and mafic magmas, and anatexis processes. Geochronological and geochemical data indicate the existence of a protracted magmatic activity related to convergent setting (long-lived magmatic arc) that forced the Vize-Pluton to undergo multi-stage melting-crystallization processes.

Thermal evolution of the North China Craton revealed by microsampling garnet geochronology on single xenoliths

Granulite xenoliths, sourced from the lower cratonic crust and brought to the Earth's surface within volcanic rocks, offer unique insights into the formation and destruction of cratons. Age determinations are essential for constructing the thermal history of cratons. However, accurate dating is complicated by the xenoliths' extended exposure to high temperatures and their complex thermal histories. Specifically, the effects of extended lower crust residency and entrainment heating on coupled Sm–Nd and Lu–Hf systematics remain to be explored. Six xenoliths hosted in the Mesozoic dioritic porphyry from the eastern North China Craton were sampled from center to edge using micro-drilling/sawing techniques. From each xenolith, two to four concentric zones were successfully extracted for coupled Lu–Hf and Sm–Nd geochronological analysis. These xenoliths predominantly exhibit a granoblastic texture, with minerals that are mostly unzoned. Textural and chemical analyses of minerals indicate a decompression process following the granulite-facies metamorphism, with subsequent multiple reheating events. Thermobarometric calculations suggest granulite-facies equilibration at temperatures of ∼750 °C and pressures of 1.2–2.0 GPa. Consistent Lu–Hf and U–Pb ages of ca. 1.7 Ga, obtained from garnet, zircon, and titanite in chemical and textural equilibrium, are attributed to granulite-facies metamorphism. The Paleoproterozoic Lu–Hf ages and the Neoproterozoic Sm–Nd dates are indistinguishable across all concentric zones within each xenolith, whereas Sm–Nd ages are consistently ∼1.0 Ga younger than the corresponding Lu–Hf ages. This discrepancy suggests a complex history for this section of the lower cratonic crust, marked by a granulite-facies metamorphic event around 1.7 Ga, followed by prolonged cooling. A significant heating event during the Tonian, likely due to regional mantle plume activity, is inferred to have partially or completely reset the Sm–Nd isochrons. This thermal event and subsequent thermal relaxation on the samples at different residence depths thereby decoupled the Sm–Nd system from the Lu–Hf system, signifying a thermal pulse at the southern margin of North China Craton. The Mesozoic entrainment heating event appears to have had minimal impact on the Lu–Hf/Sm–Nd systematics of garnet and U–Pb of zircon/titanite. Our data highlight the potential of coupled microsampling Lu–Hf and Sm–Nd geochronology on individual xenoliths to reveal tectonic episodes within the lower crust that might be undetected by accessory mineral U–Pb geochronology.

Co, Sc, and Ni enrichment in the Cagdianao nickel laterite deposit, Dinagat Islands, Philippines

Abstract Nickel laterites are soils that are derived from the weathering of mafic and ultramafic rocks. These deposits are being extracted mostly for their economic Ni and Fe content. However, in recent studies, the potential of nickel laterites to hold significant amounts of critical metals such as Sc and Co are already being investigated. In the Philippines, nickel laterite deposits form through the weathering of ophiolitic units. One of these is the Cagdianao nickel laterite deposit which was derived from the weathering of the ultramafic units of the Dinagat Ophiolite Complex in Dinagat Island, Surigao Del Norte, Philippines. The bedrock of the Dinagat Ophiolite Complex is dominantly comprised of harzburgite. This harzburgite bedrock is overlain by a nickel laterite profile consisting of horizons of Mg- and Si-rich rocky saprolite, earthy saprolite, Fe-rich limonite, and an Al-rich topsoil. Drillcores and field exposures of the nickel laterite profile were observed, sampled, and subjected to petrography, whole rock geochemistry (XRF and ICPMS), and mineral chemistry (LA-ICPMS) analyses. In terms of major elements, Fe is dominant in the limonite zone (up to 59.76 wt.%). Mg and Si are more enriched in the rocky saprolite layer (up to 28.41 and 37.41 wt.%, respectively). In terms of the critical minerals, Ni is more enriched in the saprolite zone (up to 29936 ppm) while Co and Sc are more enriched in the limonite zone (up to 1080 and 86 ppm, respectively). Elemental mapping of the bedrock samples reveals the strong affinity of Ni to olivine and serpentine. Sc was revealed to have a greater affinity with orthopyroxenes. Lastly, Co is observed to have a slight affinity with olivine. These results show a relative enrichment of Co in the profile, particularly in the limonite. Co within the laterite profile also has a very strong affinity with MnO. Similarly, the highest concentration values for Sc were also observed in the limonite. It also exhibits an affinity for Fe2O3 and Al2O3. Lastly, Ni was observed to have a strong affinity with olivine and serpentine minerals in the bedrock and the rocky saprolite horizons. Within the deposit, Ni is the main commodity while Co, Sc, and REEs can be considered as by-products.

Identification of carbonated eclogitic source for Cenozoic intraplate alkaline basalts from western Central Asia and its geodynamic implication

Carbonated eclogite has been identified as a significant component in the formation of intraplate alkaline basalts, typically attributed to stagnated subducted oceanic slabs, such as the Pacific plate beneath eastern China. However, it is unclear whether this component exists in other tectonic settings. Here, we present new zircon UPb geochronology, mineral chemistry, and geochemical analyses of Cenozoic Tuoyun basanites and alkaline basalts from western Central Asia, where stagnated subducted oceanic slabs are absent, to elucidate the source properties and associated geodynamic processes. Olivine compositions (e.g., moderate Ni concentrations, low Mn/Fe and Ni/(Mg/Fe) ratios) and whole-rock chemistry (e.g., high Fe/Mn, Ca/Al, and Zr/Hf ratios, TiO2 contents, and weak anomalies of Zr-Hf-Ti) suggest a carbonated eclogite in the mantle source of the Tuoyun basanites. Trace elements (positive NbTa anomalies and absence of positive Eu anomaly) and depleted to slightly enriched Sr-Nd-Hf isotopic compositions indicate that the basanites originated from mantle sources composed of variable proportions of altered oceanic crust (AOC) and carbonates. Synthesizing regional geochemical, geophysical studies and tectonic history, we propose that the continuous India-Eurasia collision triggered mantle upwelling, leading to the formation of a widespread carbonated eclogitic mantle source beneath western Central Asia. Our findings suggest that carbonate-rich mantle sources may also be present in areas without stagnated subduction slabs.

Sedimentary facies and mineral provenance of Upper Triassic sandstones offshore Kvitøya, Svalbard: implications for palaeogeographic interpretations in the northern Barents Shelf area

Upper Triassic (Carnian) sandstones of the De Geerdalen Formation cored south of the island of Kvitøya (80°N), north-easternmost Svalbard, are described in terms of sedimentary facies and petrography and compared regionally in the northern Barents Shelf. The succession off Kvitøya is characterized by its great thickness and is dominated by deltaic deposits with high sand content of lithic–feldspathic compositions. Comparison of sediment facies and sandstone compositions with adjacent areas suggest that the succession off Kvitøya is part of a larger delta system with its main sediment source from the east. The delta sedimentation was terminated by marine transgression in the earliest Norian. The sandstone compositions off Kvitøya differ from nearby locations by the higher content of cherty rock fragments and reworked volcanic debris in the Kvitøya sandstone, which is most distinct in the lower part of the succession. Provenance signatures are investigated by mineral–chemical analysis of detrital feldspars, rock fragments, garnet and Cr-spinel, characterizing a wide variety of igneous, metamorphic and sedimentary terranes, including palaeo-Urals and areas farther to east. Additional, more proximal sediment source areas may also have existed that could explain the increased sediment thickness and the mineralogical immature sandstone compositions of the Carnian sediments off Kvitøya.

Mineral chemistry and P–T conditions of the winchite-bearing metabasic rocks in the NE edge of the Menderes Massif (Western Türkiye)

The Menderes massif is a large metamorphic crystalline complex located in western Turkey. The massif consists of late Neoproterozoic basement (core) rocks and Palaeozoic - Cenozoic cover units that have undergone by high- and low-grade polyphase metamorphisms. Palaeozoic to Mesozoic cover units cropped out in the NE edge of the massif (east of Sivaslı) are overlaid tectonically by upper Cretaceous meta-ophiolitic rocks. The meta-ophiolitic unit comprises blocks mainly of metabasalt, metagabbro, metadiorite and metaultramafite within an intensively sheared serpentinite matrix. It also includes blocks of epidote-actinolite-schist and tremolite-actinolite-schist, which originated from basic rocks, as well as chlorite schist blocks, which originated from ultramafic rocks. Sodic-calcic amphiboles recorded in the samples of metabasalt block taken from the marble-metabasalt block boundary, at the tectonic contact where the meta-ophiolitic rocks overlap the underlying marble sequence. Sodic-calcic amphiboles were classified into winchite and ferri-winchite with relatively homogeneous TSi (7.35–8.01 a.p.f.u.), and XMg (0.69–0.80) values. P-T conditions were estimated to be around 300–400 °C and 5–6 kb based on the mineral chemical analyses of the sodic-calcic amphiboles. According to these values, the NE edge of the Menderes Massif must have undergone metamorphism under a medium-pressure (MP) greenschist facies.

Combining traditional and quantitative multiscale structural analysis to reconstruct the tectono-metamorphic evolution of migmatitic basements: the case of the Valpelline Series, Dent-Blanche Tectonic System, Western Alps

Due to the ongoing development of new technologies, many instruments are available to assist geological investigations at different scales. These techniques, including 3D outcrop modelling from aerial photogrammetry and quantitative microstructural analysis are useful in crystalline basements studies. This contribution combines traditional and quantitative multiscale structural analysis techniques to the migmatitic rocks of the Valpelline Series (Dent-Blanche Tectonic System, Western Alps). Conventional structural analysis is integrated with the extraction of structural data from 3D models of representative smooth outcrops. Quantitative microstructural and mineral-chemical analyses are combined to link structural and metamorphic evolution. This approach allows identifying and correlating foliations that developed during three tectono-metamorphic stages. The first (D1) includes solid-state deformation associated with an early foliation (S1) preserved within metabasite boudins enclosed in migmatite gneiss. The second (D2) is related to the dominant foliation in migmatite gneiss (S2), coeval with the regional scale anatexis and growth of garnet and cordierite. The third (D3) is related to the late folding of S2 and the development of a sillimanite-rich axial plane foliation (S3) which wraps around garnet and cordierite. Finally, this work discusses pros and cons of each innovative methodology, still emphasising the importance of using manually acquired field data as ground control.

First occurrence of dumortierite in Croatia: its chemical composition and appearance as an igneous mineral in leucogranite-hosted pegmatite

In this article, dumortierite from Croatia is described for the first time. Dumortierite formed in a pegmatite dyke cutting through Cretaceous two-mica leucogranite of the magmatic-metamorphic complex of Mt. Moslavačka Gora. The pegmatite dyke shows a magmatic mineral association of coarse-grained quartz, orthoclase, microcline and albite, less abundant muscovite, biotite, pinkish andalusite and blue-coloured prismatic dumortierite I crystals. Subsequent alteration by titanium-rich hydrothermal fluids led to partial replacement of dumortierite I and andalusite by secondary fibrous to acicular purple dumortierite II enriched in Mg and Ti. During temperature decrease perthite developed in feldspars and at a still later stage, sericite partially replaced not only feldspars but also andalusite and both types of dumortierite along grain boundaries and cracks. Final alteration at very low temperatures caused formation of clay minerals at the expense of feldspars. According to mineral chemical analyses, the feldspars are represented by albite and K-feldspar with a low albite component. Biotite corresponds to annite and its subhedral shape and chemical composition point to magmatic crystallisation from a peraluminous melt derived from a crustal source. Coarse muscovite flakes contain 1.31-1.48 wt.% FeO and 0.56-0.70 wt.% TiO2. Their Na/(Na+K) ratios (0.08–0.09) prove a magmatic origin, whereas lower ratios in sericite (0.04–0.06) indicate formation during retrogression. Magmatic muscovite is in textural equilibrium with andalusite, also implying an igneous origin for the latter, which belongs to the S3 textural type of andalusite in felsic igneous rocks. Electron microprobe analyses clearly show a strong positive correlation between Si tetrahedral deficiency (3-Si) and the sum of Al+Ti, (R2= 0.85) in both types of dumortierite, implying Al replacement by Ti. However, Al replacement by Ti is not restricted to Al in the octahedral position, as generally accepted, but most probably also in the tetrahedral position. Distinct pleochroic colours in dumortierite are usually explained by the [Fe/(Fe+Ti)]x100 factor, but according to this study, elevated Mg contents stabilize red to violet coloured dumortierite at higher [Fe/(Fe+Ti)] x100 factors than those previously suggested.

Metamorphic evolution of a metabasite dyke from Ogbagi Akoko area, Southwestern Nigeria

Petrography, mineral chemistry and whole rock analyses were conducted on a metabasite dyke hosted by pelitic gneiss (metapelite) in Ogbagi Akoko area with the aim of determining its metamorphic evolution. The dyke is about 40 cm wide and traceable for some meters along strike. It has a discordant contact relationship that is pencil sharp with the host pelitic gneiss and lack any internal fabric. The mineral assemblage includes: garnet +biotite + plagioclase + quartz + orthopyroxene + K-feldspar + ilmenite, with apatite occurring as an accessory mineral. Plagioclase has anorthite content of about 76 (An76) suggesting bytownite (An76 Ab24 Or0) while garnets are poikiloblastic almandine-pyrope rich with XFe of 0.73-0.75. Orthopyroxene has a composition of Wo0 En50 Fs50 suggesting hypersthene that is depleted in Ca. The mineral assemblage, presence of bytownite, absence of amphibole and lack of internal fabric indicate that the rock has undergone metamorphism at a high temperature and moderate pressure without deformation at granulite facies metamorphism. The absence of deformation structure in the dyke is an indication that the intrusion occurred after the cessation of the regional metamorphism but prevalent high temperature that recrystallized the rock. The whole rock composition and some elemental ratios of the dyke indicate that the metamorphism had little or no effect on the bulk chemistry of the rock.

Origin and evolution of lithospheric mantle beneath the juvenile Arabian–Nubian Shield: Evidence from the Natash peridotite xenoliths, Southern Eastern Desert, Egypt

Compared with the Archean cratonic mantle, much less is known about the genesis and composition of the subcontinental lithospheric mantle (SCLM) beneath the juvenile terranes. In this study, we present petrology and mineral chemistry analyses of peridotite xenoliths carried by Cretaceous volcanics from the Natash area in the western Arabian–Nubian Shield (ANS). Combined with mantle xenoliths from the eastern ANS, we aim to constrain the nature, origin, and evolution of SCLM beneath the juvenile terrane. The Natash peridotite xenoliths, including well-preserved clinopyroxene (Cpx) and spinel (Sp), are categorized into two groups. Group A peridotites display exceptionally high Mg# (molar100 × Mg/(Mg + Fetotal)) in Cpx (95.6–96.7) and Cr# (molar100 × Cr/(Cr + Al)) in Sp (45.5–51.7), signifying a high degree of melting and refractory nature. Cpx in Group A demonstrates low Ti/Eu (532–1785) and high (La/Yb)N (5.34–26.29) ratios, indicative of carbonatitic metasomatism. Comparatively, Group B peridotites exhibit relatively high Mg# in Cpx (93.8–95.5) and Cr# in Sp (15.9–26.2), indicating a low degree of melting and fertile nature. Cpx trace element patterns subdivide Group B into three sub-groups. Cpx in Group B1 are characterized by high Ti/Eu (3934–5622) but low (La/Yb)N (0.91–2.98), implying silicate melt metasomatism. Both Groups B2 and B3 Cpx show steep rare earth element (REE) patterns, negative anomalies in high field-strength elements, and high (La/Yb)N (3.62–7.57). However, Cpx in B3 exhibit higher Ti/Eu ratios and water-soluble element contents than those in B2 peridotites. In addition, the spoon-shaped REE patterns are prominently unique to Cpx in Group B3. Hence, it is inferred that Group B2 were influenced by carbonatitic melts, whereas the evolved small-volume CO2-H2O-rich fluids infiltrated into Group B3 samples. Furthermore, the high Sr contents (71–404 ppm) but low 87Sr/86Sr (0.7003–0.7034) ratios of Cpx in Natash peridotites suggest that the various metasomatic agents all originated from the asthenosphere. Collectively, the Natash peridotite xenoliths exhibit similar nature and metasomatism processes with those from Cenozoic volcanics in the eastern ANS, and they all show affinity to continental peridotites. The pMELTS simulation suggests that the refractory peridotites have a high melting pressure (typically >3 GPa), while the fertile samples register a low melting pressure. Consequently, we infer that the SCLM beneath the juvenile ANS was formed through the cooling of upwelling asthenosphere, incorporating the ancient mantle fragments, and subsequently underwent asthenosphere-derived carbonatitic and silicate melt/fluid metasomatisms.

WinPclclas, a Windows Program for Pyrochlore Supergroup Minerals

Abstract A Microsoft® Visual Basic program, WinPclclas, has been developed to calculate the chemical formulae of pyrochlore supergroup minerals (PSM) based on data obtained from wet-chemical and electron-microprobe analyses. These are also classified following the nomenclature scheme adopted by the Commission on New Minerals, Nomenclature and Classification (CNMNC) of the International Mineralogical Association for PSM (IMA-10) and including both subsequent group and species updates. The program considers classification among the 33 IMA-approved PSM, as well as ten species that have not been approved, adhering to the general formula A2B2X6Y and considering the dominant ions at the A, B, and Y sites. It considers PSM represented by the pyrochlore, microlite, roméite, elsmoreite, and betafite groups, along with unassigned members of the ralstonite and coulsellite groups. Mineral formulae of the PSM are calculated based on the ideal number of B cations being two apfu, owing to the potential for vacancies at the A, X, and Y sites. WinPclclas operates in four stages: (1) it estimates cation and anion contents provided by input chemical data; (2) it determines the dominant cation and anion at the A, B, and Y sites; (3) it assigns the PSM to one of the seven groups, based on the dominant cation at the B site (i.e., W6+, Nb5+, Ta5+, Sb5+, Ti4+, Al3+, and Mg2+); and (4) it classifies the pyrochlore species into an appropriate group, based on the dominant cation at the A site and the dominant anion at the Y site. The H2O (wt.%) content for the PSM is estimated by stoichiometric constraints. WinPclclas allows users to: (1) enter up to 51 input variables for mineral-chemical analyses; (2) type and load multiple PSM compositions in the data entry section; (3) edit and load the Microsoft® Excel files used in calculating, classifying, and naming the PSM, together with the total monovalent to hexavalent cation, and (4) store all the calculated parameters in the output of a Microsoft® Excel file for further data evaluations. The program is distributed as a self-extracting setup file, including the necessary support files used by the program, a help file, and representative sample data files.

Genesis of Sulfide Mineralization in the Gallala Area Kurdistan Region, Iraq: Constraints from Major and Trace Elements of Sulfide Ore Mineralization and their Host Rocks

This article presents and interprets new geochemical data from the Gallala sulfide mineralization, situated in the Choman District of the Kurdistan Region of Iraq close to the Iraq and Iranian border. The host rocks belong to the Walash-Naopurdan Group, which developed in the Paleocene-Eocene age in the Zagros Suture Zone. The ore mineral assemblage of the Gallala area consists of pyrite, chalcopyrite, sphalerite, and magnetite. The mineral chemistry and geochemical analysis indicate that there is a significant variation in concentrations of pyrite, chalcopyrite, sphalerite, and magnetite from the Gallala mineralization. The trace element characteristics of the sulfide mineralization and their host rocks indicate that the ore-forming materials were derived from hydrothermal fluids being interacted with the igneous rocks. The trace element signatures and REE distributions of the studied samples, tectonically lead to suggest island-arc and back-arc environments in the Gallala area. Additionally, the REE patterns of the Gallala sulfides indicate the ore-forming fluids are related to arc-related hydrothermal systems. The integration of geochemical features along with the chemistry of ore mineralization such as the Selenium/Sulfur ratio of pyrite, Co/Ni ratios from both pyrite and chalcopyrite, the Zn/Cd values from the sphalerite, and the petrogenetic discriminate diagrams of magnetite reveal that the genesis of the sulfide mineralization can be attributed to volcanogenic to hydrothermal ore-formations with high to medium temperatures origin.

Mineral Chemistry of Pyrochlore Supergroup Minerals as Records of Nb Mineralization Processes in NYF-Type Pegmatites: A Case Study of the Emeishan Large Igneous Province, SW China

Alkaline igneous rocks have become a potentially important source of Nb, except for the carbonatites. The metallogenetic mechanism of Nb during the magmatic-hydrothermal evolution of alkaline rocks remains ambiguous. From the perspective of Nb minerals, the mineral chemistry of pyrochlore supergroup minerals provides the mineralogical evidence for indicating the respective contributions of magma and hydrothermal fluids to Nb mineralization. In the Miyi County of the Panzhihua-Xichang (Pan-Xi) area, the central zone of the Permian Emeishan large igneous province (ELIP) in SW China, hundreds of Nb-Y-F mineralized pegmatites (NYF-type) are exposed. This study conducted in situ mineral chemistry analyses on four types of pyrochlores to elucidate the Nb mineralization process. Both Pcl-I and Pcl-II exhibit well-developed oscillatory zoning (OZ), representing magmatic pyrochlore formed through disequilibrium crystallization in an oscillatory environment. Pcl-III, with a homogeneous and less variable composition, is also considered of magmatic origin due to its coherent chemical evolution with Pcl-II. Pcl-IV is considered of hydrothermal origin based on its irregular zoning texture, extremely high Na2O contents, and compositional gap compared with magmatic types. The decrease in TiO2 contents, coupled with the increase in Na2O, F, and Nb2O5 contents from Pcl-I to Pcl-III and from the core to the rim of zoned Pcl-II, indicates that fractional crystallization facilitates the crystallization of albite and the enrichment of volatiles, as well as the precipitation of Nb from the early to late stages. During the magmatic-hydrothermal transition stage, the reductive, Na- and F-enriched fluid transports Nb more effectively, leading to further Nb enrichment in pyrochlore. Consequently, there are two-stage Nb mineralization processes associated with the magmatic-hydrothermal evolution in the Miyi pegmatite, with the primary magmatic ore assemblages being the dominant Nb mineralization, which may be a general model for the mineralization of NYF-type pegmatites.

Petrogenesis of Neoproterozoic high-K intrusion in the southwestern Yangtze Block, South China: Implication for the recycled subducted-sediment in the mantle source

The study of K-enriched intrusive rocks is essential for deciphering mantle metasomatism beneath active continental arcs. In this contribution, high-precision zircon U–Pb–Hf isotope, whole-rock geochemistry, Sr–Nd isotope, and mineral chemistry analyses were performed to evaluate the petrogenesis and geodynamic system of the Yunnongfeng intrusion on the southwestern margin of the Yangtze Block. The Yunnongfeng intrusion consists of a high-K to shoshonitic rock assemblage with variable lithology from gabbro-diorite to granite. Zircon U–Pb dating gives concordant crystallization ages of ca. 782.5 ± 3.8 Ma for gabbro-diorite, ca. 774 ± 4.1 and 776 ± 4.1 Ma for diorite, ca. 770 ± 4.7 Ma for quartz monzonite, ca. 763 ± 3.4 Ma for quartz syenite, and ca. 764 ± 16 Ma for granite. These samples also show similar Sr–Nd, and Lu–Hf isotopic compositions, implying a common magma source. The similar crystallization age and regular variation of major and trace element contents suggest that these rocks were formed through fractional crystallization of cogenetic primitive mantle magmas. The enriched εNd(t) (−5.7 to − 5.1) and εHf(t) (−6.7 to − 1.2) values, high Rb/Y and Th/La ratios, slight Nd–Hf decoupling, and high-K and Th contents demonstrate that their lithospheric mantle source was enriched by slab-related fluid and sediment-related melt. The samples also exhibit remarkable enrichment in large-ion lithophile elements and depletion in high-field-strength elements, indicative of subduction-related arc magmatism. Taking into account previous studies, we suggest that the western margin of the Yangtze Block experienced a long-term subduction process during the Neoproterozoic, and the Yunnongfeng intrusion formed in an extensional back-arc basin. Based on the K-enriched mafic–intermediate rocks from the western margin of the Yangtze Block commonly show high K2O/Na2O, Rb/Sr, low Ba/Rb ratios, and enriched εNd(t) values, our study, coupled with numerous previous reports, proposes that the K-enrichment resulted from the breakdown of phlogopite, owing to subduction-related sediment melt reacting with peridotite in the mantle source area.

Thermal Evolution of the Lithosphere‐Asthenosphere Boundary Beneath Arc and Its Geodynamic Implications: Depth Variation of Thermal Histories of Mantle Xenoliths From Ichinomegata, Northeast Japan

AbstractQuantitative reconstruction of thermal history recorded in mantle xenoliths is imperative for understanding the temporal change of thermal state and dynamics of the lithosphere‐asthenosphere boundary (LAB). We challenged this problem in the arc settings by examining nine spinel peridotite xenoliths from Ichinomegata maar in the back‐arc side of Northeast Japan Arc. Extensive mineral chemical analyses combined with the derivation depths of the xenoliths revealed a depth‐dependent variation of chemical zoning patterns in olivine and pyroxenes. The depth variation of thermal histories of the Ichinomegata xenoliths was decoded by applying diffusion‐controlled reaction modeling to reproduce the zoning patterns. The decoded thermal events in the order of occurrence are (a) ∼14 million years of cooling causing lithosphere thickening up to ∼55 km depth, (b) subsequent ∼12 thousand years of heating from the underlying asthenosphere resulting in lithosphere thinning up to the depths of ∼40 km, and (c) 1–68 days of heating during xenolith transportation by the host magma. The duration of the lithosphere thickening is consistently explained by the period of the Japan Sea opening. On the other hand, the timescale of the lithosphere thinning is too short to be explained by heat conduction through the ∼15 km thick LAB and requires a more effective heat transportation mechanism such as direct magma injection into the LAB or significant viscosity reduction of the mantle peridotite aided by the pervasive permeable flow of silicate melt.

A wealth of P–T–t information from metasediments in the HP–UHP terrane of the Pohorje Mountains, Slovenia, elucidates the evolution of the Eastern Alps

AbstractContrasting views exist in regard of the evolution of metamorphic rocks in the southeastern Pohorje Mountains (Mts), located in the southeastern Eastern Alps. Major debated points are whether micaschists have experienced ultrahigh‐pressure metamorphism in the Late Cretaceous (Eo‐Alpine) and whether they were continuously exhumed or experienced a multiple subduction–exhumation process from that time on. Therefore, we studied micaschist sample 18Slo39 with two generations of garnet and phengitic muscovite from this area. Our detailed study of this rock included petrographic observations, chemical analyses of minerals with the electron microprobe, pseudosection modelling, conventional geothermometry, and monazite in‐situ U‐Th‐Pb dating using laser‐ablation inductively coupled plasma (ICP) mass spectrometry. The following results were obtained: The studied micaschist was subject to a peak pressure of 1.31 ± 0.14 GPa at 603 ± 26°C in Eo‐Alpine times: 90.62 ± 2.78 (2σ) Ma (Stage I). Contact metamorphism at pressure–temperature conditions of 0.66 ± 0.10 GPa and 577 ± 23°C was induced by the intrusion of the Pohorje pluton (Stage III). We determined an early Miocene age of 18.33 ± 0.43 (2σ) Ma for this intrusion. Based on this study and the previously reported data for a micaschist (16Slo12) taken in the vicinity of sample 18Slo39, a geodynamic model is proposed for the region of the Pohorje Mts considering Eo‐Alpine subduction of oceanic crust and European continental crust, of which the micaschist was part of. Another high‐pressure event in the Eocene (Stage II) was the result of intracontinental subduction because of transpression by the Periadriatic fault system that separates the Eastern Alps from the Southern Alps. This type of subduction gave rise to magma generation and ascent to form the Pohorje pluton, which caused contact metamorphism in its vicinity.