Fractional Crystallization Research Articles

Characteristics and formation of rare-metal pegmatites and granites in the Duanfengshan-Guanyuan district of the northern Mufushan granite complex in South China

The Mufushan area, which has abundant rare-metal pegmatites within and around the Mufushan Granite Complex, has become a major target for Ta-Nb-(Li-Be) exploration in South China. The age and origin of the pegmatites and associated rare-metal mineralization are still under debate. Here, we report the in situ U-Pb ages and geochemical characteristics of granites and pegmatites in the Guanyuan and Duanfengshan districts, which are located in the central and northern parts of the Mufushan Complex. Combined zircon, apatite and monazite U-(Th)-Pb dating revealed that biotite, two-mica, and muscovite granites from the Guanyuan and Duanfengshan districts were emplaced at 143–139 Ma, which overlaps with the U-Pb ages of columbite-group minerals (CGM) from different internal zones of the Duanfengshan pegmatites (142–140 Ma). Whole-rock major and trace element compositions and Sr-Nd-Hf isotope data reveal that the granites and pegmatites experienced continuous evolution from biotite, two-mica, and muscovite granites to pegmatite and that the magma originated from the partial melting of mica schists that are abundant in the Mufushan area. Temporal, chemical and mineralogical evidence indicates a genetic link between muscovite granite and Ta-Nb pegmatites. The textures and chemical compositions of CGM from different pegmatites exhibit features typical of magmatic CGM, indicating that fractional crystallization was the driving force that promoted Ta-Nb enrichment. The increasing alumina saturation index [ASI: molar Al/(Ca–1.67P + Na + K)] of pegmatitic melt due to albite crystallization may have been the main factor controlling CGM deposition, explaining why major Ta-Nb mineralization is bound to albite pegmatites. The Duanfengshan and other rare-metal pegmatites in the Mufushan area are derivatives of the most evolved granitic facies (i.e., muscovite granite) of the Mufushan Complex. The Duanfengshan and Renli pegmatite fields indicate that the Early Cretaceous (∼140 Ma) may have been an important, underappreciated epoch for the formation of pegmatite-related rare-metal resources in the Mufushan area and beyond in South China.

The influence of olivine settling on the formation of basaltic cumulates revealed by micro-tomography and numerical simulations

The speed at which crystals settle in magmatic reservoirs affects the solidification rate of magmas and their differentiation. Despite extensive prior work on the subject, most of our quantitative understanding of the process is still restricted to treating crystals as spherical particles and does not address the geometric complexities of natural crystals. Here, we use three-dimensional (3D) X-ray microcomputed tomography (X-μCT) observations on olivine crystals from Kīlauea Volcano (Hawai‘i) to document their highly intricate and variable geometries, and the textural growth relationships between the olivine crystals and their inclusions (melt, spinel, and fluid/vapor bubbles). Olivine crystals generally have clustered polyhedral or skeletal shapes, which reflect variable magmatic conditions (or growth rates) during their formation. The cumulative presence of spinel, melt, fluid, and vapor inclusions affects the density of the host crystals by up to 6% relative, and thus plays a limited role on modifying crystal settling rate. In contrast, the overall crystal shape plays a major role. We performed numerical simulations employing a finite element method to investigate the effect of crystal morphology on settling rate and the evolution of the particle volume fraction in a magmatic convective layer. We show that for all olivine geometries investigated, the settling velocity is highest when the long axis of the crystal is aligned with the flow direction of the melt. Increasing the aspect ratio of the olivine tends to decrease its settling velocity and results in an increase in the influence of its orientation on the terminal velocity (UT). Extrapolation of the simulation results to variable particle volume fractions (Φ = 0–0.5) indicates high crystal settling rates (UT = ∼9.7 × 10−6–1.4 × 10−5 m/s) that are used to estimate the timescales for the formation of olivine cumulates in natural melt-dominated basaltic systems. The formation of olivine cumulates is therefore rapid, potentially leading to the accumulation of a crystal layer at the bottom, where the frictional contacts between the crystals exert a rheological lock-up acting against further convection. Crystal accumulation in the locked layer (parametrized with the solid/liquid volume ratio in the reservoir) is a function of the reservoir size and crystal fraction, and takes a few years in small reservoirs (<1 km thick) and a few decades in larger reservoirs (several kms thick). We propose a calibration of olivine suspension timescales for mafic magma reservoirs (based on the knowledge of the particle volume fraction, reservoir height, and olivine morphology). This calibration is used to estimate the rate of cumulate build-up, and can help interpret crystal size distributions in the framework of crystal suspension times.

The 2023 Litli-Hrútur eruption of the Fagradalsfjall Fires, SW-Iceland: Insights from trace element compositions of olivine

This study provides data on the trace element composition of olivine from olivine tholeiitic basalts sampled during the July–August 2023 Litli-Hrútur eruption of the Fagradalsfjall Fires in the Reykjanes Volcanic Belt. Chemistry of the Litli-Hrútur olivine is characteristic for volcanic olivine crystals that represent products of magmatic crystallisation. The investigated olivine megacrysts show forsterite (Fo) content in the range of 81 (rims) to 85 (cores) mole percent [defined as Fo = Mg/(Mg + Fe)]. Olivine Ni concentrations (1540–1840 ppm) correlate positively with the Fo contents. In addition, Ca contents show a range from 1890 to 2460 ppm at relatively low Ti concentrations. Olivine from the Litli-Hrútur samples shows an equilibrium with peridotitic mantle melts, yet the data show that the 2023 Litli-Hrútur and the 2022 Meradalir olivine populations crystallised from compositionally more evolved magma batches than olivine crystals from the 2021 Geldingadalir eruption of the Fagradalsfjall Fires. These results imply that magmatic differentiation has taken place between the initial 2021 events and the subsequent 2022 and 2023 eruptions as a result of crystal–liquid fractionation, shifting the overall magma chemistry towards more evolved compositions with time. This implies that fractional crystallisation in sub-alkaline magma reservoirs operates on the scale of years, which is a fundamental advance in our understanding of these common magmatic systems.

Olivine in ultramafic rocks from the Polaris Alaskan-type intrusion: A geochemical record of open-system crystallization, diffusional re-equilibration, mantle source, and redox conditions in primitive arc magmas

Olivine in cumulates from the Early Jurassic Polaris Alaskan-type ultramafic-mafic intrusion in the North American Cordillera displays a wide range of textures and compositions produced in a dynamic crystallization environment as part of a transcrustal arc magmatic system. Major, minor, and trace element analyses of olivine were determined using combined electron probe microanalysis (EPMA) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) to assess the utility of olivine as a petrogenetic indicator in ultramafic intrusions. High forsterite contents (>Fo87) of olivine from dunite, olivine wehrlite, and wehrlite indicate that the parent melts were primitive in composition and that they may represent intrusive analogues to extrusive arc picrites found elsewhere in the Cordillera. Forsterite-Ni systematics (Fo92–80, Ni = 3000–300 ppm) show fractional crystallization-controlled evolution from dunite to olivine wehrlite to wehrlite through olivine clinopyroxenite. Low-Ni olivine (Fo84–80, 500–300 ppm) in magnetite-olivine clinopyroxenite indicates the effects of sulfide melt saturation and Ni-depletion of the residual magma. Entrainment of high-Fo olivine in evolved melts and mixing between fractionated and primitive magmas explains olivine compositions with Ni concentrations (1000–3000 ppm) in excess of those predicted by fractional crystallization models. Extensive subsolidus diffusion of Mg, Fe, Ni, Mn, Ca, Cr, Al, and Li occurred during crystallization and cooling of olivine. Uniform concentrations of Mg, Fe, Ni, and Mn in individual samples and across crystals of olivine indicate complete equilibration in the consolidating cumulate pile. Calcium, Cr, and Al from Polaris olivine (e.g., typically <1000 ppm Ca, <100 ppm Cr and Al), and from plutonic olivine in general, are depleted relative to volcanic olivine as the result of diffusional re-equilibration with interstitial melt and other co-crystallizing phases (Cr-spinel, clinopyroxene). Ratios of first-row transition elements (Mn, Zn, Fe, Co, Ni) in olivine were modified during intracrustal processes (e.g., fractional crystallization, diffusion), however, ratios from the most primitive olivine are indicative of primary mantle signals. Lithium concentrations in olivine (2–12 ppm) show evidence for subsolidus diffusive re-equilibration with Li-enriched melts. Ratios of V/Sc (0.03–0.5) are consistent with relatively oxidized parent magmas and arc mantle sources to Polaris and Alaskan-type intrusions. The Polaris parent magmas ascended through the uppermost mantle and lowermost crust on sufficiently short timescales to avoid significant magmatic differentiation prior to emplacement at a depth of ≤15 km. The findings of this microanalytical study highlight the utility of olivine as a petrogenetic recorder of primary magmatic and high-temperature diffusional processes in ultramafic plutonic rocks and contribute to our understanding of the evolution of primitive arc magmas.

Origin of granitoids and coeval mafic microgranular enclaves in the East Kunlun Orogen, northern Tibetan Plateau: Insights from petrography, U-Pb geochronology, geochemical and isotope analyses

Granitoids and coeval mafic microgranular enclaves (MMEs) provide important insights into petrogenesis and crustal evolution. In the eastern sector of the East Kunlun Orogen, the Halazha (HLZ) pluton contains abundant MMEs, recording magma mingling processes. The HLZ pluton comprises quartz diorites and granodiorites, whereas the MMEs have a gabbroic-dioritic composition. This paper provides a detailed description of the petrography and mineralogy of the HLZ pluton and MMEs, and presents new ages and geochemical data. The zircon U–Pb dating results indicate that quartz diorites and granodiorites are ranging from 243 ± 2 Ma to 244.8 ± 1.3 Ma and from 233.3 ± 1.1 Ma to 233.6 ± 1.5 Ma, respectively. The zircon ages of the coeval MMEs are identical to the host rocks, i.e., 244.5 ± 1.1 Ma − 244.5 ± 1.2 Ma, and 233.7 ± 1.3 Ma, respectively. Both quartz diorites and granodiorites contain hornblende, display metaluminous characteristics with average A/CNK values of 0.93 and 0.99, respectively, and thus belong to I-type granite. Both of them are enriched in large-ion lithophile elements such as Rb and Ba and depleted in high-field-strength elements such as Nb and Ta. In addition, they both have low εHf(t) values, ranging from −5.6 to −1.7 and −5.4 to −1.79, respectively. Results suggest that HLZ pluton is derived from magmas formed by the partially melting juvenile mafic lower crust. Quartz diorites experienced hornblende accumulation for its low SiO2 contents. Whereas, the high Sr/Y ratio of granodiorites attributes to the fractional crystallization of apatite. Notably, the crystallization pressure and temperature (average 3.43 kbar and 764 °C) of the hornblende xenocrysts in MMEs is close to it of the hornblende phenocryst in quartz diorite (average 3.68 kbar and 766 °C). This similarity indicates that MMEs in the quartz diorites resulted from magmatic mingling between the mafic magma and the host rock within the deep crust. The hornblende xenocrysts present in MMEs of the granodiorites contain a higher number of inclusions, reveal higher crystallization pressures (average 2.73 kbar) and temperatures (average 825 °C) compared to their host rocks (average 1.35 kbar and 702 °C). These results suggest that MMEs in granodiorites underwent two distinct magmatic mixing processes: the magmatic mixing of mafic magma in the deep crust and then during the upwelling process after this mixed mafic magma entered the granodiorites.

Tectonic and Crustal Processes Drive Multi-Million Year Arc Magma Evolution Leading up to Porphyry Copper Deposit Formation in Central Chile

Abstract Subduction zone magmatism is a major control of volcanism, the generation of modern continental crust and the formation of economically important porphyry Cu–(Mo–Au) deposits. Reading the magmatic record of individual arc segments and constraining the rates of magmatic changes are critical in order to fully understand and quantify the processes that drive magma evolution in subduction settings during arc growth. This study focuses on the San Francisco Batholith and the Rio Blanco-Los Bronces porphyry deposit cluster in central Chile, which provides an igneous rock record over ~13.5 Myr of arc evolution. We use whole-rock geochemistry, zircon geochronology and Hf isotope geochemistry to track changes in the crustal magmatic system of this arc segment during crustal thickening and porphyry Cu deposit formation. By combining the analytical dataset with Monte Carlo fractional crystallisation and assimilation fractional crystallisation modelling, we test a model for significant crustal involvement during magma evolution. Systematic and continuous increases in Dy/Yb, La/Yb, V/Sc and Sr/Y in the magmas over time indicate a transition in the main fractionation assemblage from plagioclase-dominated to amphibole-dominated that reflects deeper crystallisation and/or a higher meltwater content. Concomitant decreases in εHf and Th/La as well as increasing Ba/Th are best explained by assimilation of progressively deeper crustal lithologies from low (Chilenia) to high Ba/Th (Cuyania) basement terranes. Our study highlights that an increasingly hydrous magma and a deepening locus of crustal magma differentiation and assimilation, driven by crustal thickening contemporaneous with increased tectonic convergence and ingression of the aseismic Juan Fernandez ridge, can account for all investigated aspects of the multi-Myr magmatic evolution leading up to the formation of the Rio Blanco-Los Bronces porphyry Cu deposits. Our findings corroborate the importance of high-pressure differentiation of hydrous magma for the formation of Andean-style porphyry deposits. Once magmas favourable for porphyry Cu mineralisation were generated in the lower crust, multiple episodes of efficient magma migration into the upper crust fed several, discrete, shallow magmatic-hydrothermal systems over ~3.5 Myr to form the world’s largest known Cu resource at Rio Blanco-Los Bronces.

The role of fractional crystallization of water-rich magma in forming high Sr/Y intermediate-silicic rocks in the Beishan orogen, NW China

The petrogenesis of intermediate-silicic rocks with high Sr/Y ratios that are closely associated with porphyry Cu-Au mineralization and TTGs remains uncertain. This study presents new geochronological and geochemical data for high Sr/Y granodiorites and associated mafic microgranular enclaves (MMEs) from the Late Devonian–early Carboniferous Suanjingzi batholith in the Beishan orogen, NW China. The MMEs, dioritic and fine-grained, share mineral assemblages with their hosts but contain more amphibole. Similarities in ages and Sr-Nd-O isotopes between the MMEs and their hosts indicate that they share a common magma source. Our geochemical studies and quantitative modeling imply that upper crustal fractional crystallization of water-rich magma, represented by the associated MMEs, played a crucial role in forming the Late Devonian–early Carboniferous high Sr/Y rocks in central Beishan. High H2O contents promote amphibole crystallization and delay plagioclase appearance, giving rise to higher Sr and lower Y contents in evolved magma. Additionally, titanite fractionation can contribute to high Sr/Y ratios by decreasing Y contents. The MMEs, the best available proxy for the parental magma, originated from the partial melting of a mantle wedge metasomatized by subduction fluids. This study emphasizes the significance of upper crustal fractional crystallization of water-rich magma in forming high Sr/Y rocks. The possible increment caused by amphibole-dominated fractionation within the upper crustal level should be considered when employing Sr/Y ratios to quantify crustal thickness. Moreover, we argue that Late Devonian–early Carboniferous magmatism in central Beishan occurred in a continental arc setting, providing a stronger basis for understanding the Paleozoic tectonic evolution of the Beishan orogen.

The Esquinzo Ultra-Alkaline Rock Suite of Fuerteventura Basal Complex (Canary Islands): Evidence for Origin of Carbonatites by Fractional Crystallization

The origin of the carbonatites that appear on Earth is one of the most controversial current topics in the petrogenesis of igneous rocks. Situated in the northern sector of the Basal Complex of Fuerteventura (Canary Islands), the Miocene Esquinzo ultra-alkaline plutonic rock complex is composed of pyroxenites, melteigites-ijolites-urtites, malignites-nepheline syenites, carbonatites, silicocarbonatites, nephelinites and nepheline phonolites. This work tries to establish the genesis of this massif of ultra-alkaline rocks with associated carbonatites from Fuerteventura (which are very rare in the oceans). The geochemical characteristics of these rocks and the minerals that are included in them have allowed us to establish their origin. This complex was generated by three successive magmatic events associated with differentiation of melanephelinite magmas emplaced in the oceanic crust. Silicocarbonatite and calciocarbonatite (sövites) dykes are related to the first magmatic event and were formed by fractional crystallization of H2O- and CO2-rich ijolite magmas. The melanephelinite magmas that formed these plutonic ultra-alkaline rocks were apparently generated as partial melts of asthenospheric mantle, which assimilated enriched lithospheric mantle material as they ascended. The upwelling of this large body of anomalous asthenospheric Miocene material exceeded the deformation associated with plate motions and led to an oceanic rifting event in Fuerteventura.

Plagioclase as archive of the incremental assembly of the Quxu batholith, South Tibet: Implication for the nature of magma reservoir

The formation of magma reservoir and resultant construction of large batholith are increasingly recognized as long-term incremental processes. Here we employed back-scattered electron and cathodoluminescence images, in-situ major and trace elements, and Sr isotopes of plagioclase for five lithological groups from the Quxu complex batholith (south Tibet), which shed new light on the nature and incremental construction processes of batholith. Our results show that plagioclases display diverse textures and show systematic differences in geochemistry and Sr isotopes for different lithologies, indicating that their host rocks originated from multiple magma sources and/or underwent distinct magmatic processes. Plagioclases in Group I granodiorites and Group III mafic dykes and mafic magmatic enclaves exhibit comparable textural features (e.g., resorption and sieved textures) and share similar Sr (< 1500 ppm) and Ba (< 200 ppm) contents, and 87Sr/86Sr ratios (ISr) (0.7035–0.7050) at given lower An (20–50) values, suggesting that they were evolved from similar mafic magma sources. The significant variations in An (20–90), Sr and Ba contents of plagioclase in Group III indicate both fractional crystallization and magma mixing. Plagioclases in Group II monzogranites have a similar An ranges to Group I but higher Sr (900–2200 ppm) contents and ISr (mostly 0.7045 to 0.7066) values, suggesting that they formed from partial melting of juvenile mafic crust without significant mantle contribution. Plagioclases in Group IV granodiorites and Group V monzogranites exhibit higher Sr (500–3000 ppm) contents than other groups at given An values. Their ISr values fall within the range of Group II, indicating a similar magma source. Abundant plagioclases displaying normal and oscillatory zonings in them implies that fractional crystallization occurred, while the presence of typical glomerocrysts in Group V indicates mush disaggregation. The simulation results of the trace elements indicate that the different lithologies of the Quxu batholith represent different states of magma reservoirs, corresponding to crystal mushes with varying degrees of extracted melts. The incremental growth processes of lager batholith operate as an open system, in which magma convection, mixing and recharge, crystal accumulation, recycling and reaction with melts, and mush disaggregation commonly occur.

Geochemical fingerprinting of continental crust trapped in Cadomian volcanic arcs along northern Gondwana

During the Ediacaran to Cambrian periods, the extensive Avalonian–Cadomian accretionary orogen formed along the northern margin of the Gondwana (Pannotia) supercontinent. One of the best-preserved magmatic arcs within this orogenic system is the Davle volcanic complex (DVC) in the Teplá–Barrandian unit of the Bohemian Massif. Using detailed field observations, petrography, major/trace element concentrations, Nd–Hf isotopic compositions as well as U–Pb zircon dating, we interpret a complex evolutionary history of the DVC as comprising three main stages. The first stage (∼610–570 Ma) is represented by a volcano-plutonic association of andesite, dacite, rhyolite and tonalite–trondhjemite–granodiorite (metamorphosed to orthogneiss). A wide range of major/trace element contents together with highly variable εNd values (+3.6 to –5.1) suggest derivation from a juvenile (mantle-derived) source with subsequent assimilation of cratonic crust during magma emplacement, also supported by the modelling of the assimilation–fractional crystallization (AFC) process. The second stage (∼580–560 Ma) is characterized by a gradual termination of the volcanic arc activity, followed by a deposition of marine siliciclastic succession comprising, from the bottom to the top, laminated tuffs, silicified black shales (Lečice Member), and a thick turbidite greywacke–shale–conglomerate sequence (Štěchovice Group). The third stage of poorly constrained age (∼570–500 Ma) is represented by an intra-arc extension and intrusion of juvenile trondhjemite and related rhyolite dykes (εNd +4.8 to +8.4). Finally, we compare these findings with zircon U–Pb ages and whole-rock Nd isotopic data from other Cadomian terranes and propose that the cratonic crust played an important role in recycling along the whole orogenic belt. Thus, we conclude that the Cadomian Orogen formed as a collage of fringing (such as modern Japan, Taiwan, or Philippines) and continental (as modern Andes) arcs of variable evolutionary stages rather than as a belt dominated by intra-oceanic island arcs.

The Role of Crustal Contamination throughout the 1329–2005 CE Eruptive Record of Mt. Etna Volcano, Italy

Abstract The nearly continuous volcanic eruption record at Mt. Etna dating back ~700 years provides an excellent opportunity to investigate the geochemical evolution of a highly active volcano. Of particular interest is elucidating the cause of selective enrichment in alkali elements (K and Rb) and 87Sr/86Sr observed in various episodes of past activity. More recently, this alkali enrichment trend started to manifest in the 17th century and accelerated after 1971, and was accompanied by an increase in the volume, frequency, and explosivity of eruptions. Explanations for this signature include recharge of alkali-enriched magmas and/or crustal contamination from the subvolcanic basement. This study quantitatively examines the role of crustal contamination in post-1971 Etnean magma compositions via hundreds of open-system phase equilibria and trace element calculations based upon whole-rock major oxides, trace elements, 87Sr/86Sr ratios, and mineral compositional data. Available pre-1971 petrochemical data are satisfactorily reproduced by fractional crystallization of a high whole-rock MgO (12–17 wt.%), Ni (135–285 ppm), and Cr (920–1330 ppm) parental magma composition that is documented in Etna's ~4-ka fall-stratified deposit. Observed post-1971 whole-rock and glass trends and phase equilibria are reproduced via modeled assimilation of a skarn and flysch mixture, lithologies that represent the uppermost 10 to 15 km of sedimentary rocks beneath Etna. Notably, models show that K2O (wt.%) and Rb (ppm) behave incompatibly during partial melting of skarn/flysch. Additionally, the observed elevation of 87Sr/86Sr in post-1971 samples is consistent with the addition of radiogenic Sr from wallrock partial melts. In best-fit models, which yield observed post-1971 K2O, Rb, and 87Sr/86Sr trends, ~17% anatectic melt is assimilated and there may be a subordinate stoped wallrock component of ≤2% (percentage is relative to the starting mass of pristine magma). Previous work has shown that metasomatized spinel lherzolite and garnet pyroxenite can be melted in different proportions to reproduce long- and short-term changes observed in Etna’s geochemical products. We propose that the alkali enrichment signature observed after 1971 can be fully explained through the combination of mantle heterogeneity and crustal contamination. In particular, up to ~20% crustal input coupled with mantle heterogeneity of primitive melts explains the geochemical signals quite well. The influence of crustal contamination on post-1971 lavas is, in part, the result of frequent recharge of magmas that thermally primed the middle to upper crust and enhanced its partial melting.

Partial melting of amphibolite lower crust: A potential magma source for granite-related W mineralization

Magmas for the granite-related tungsten deposits (GTD) are commonly considered to be generated from the upper to middle crustal metasedimentary protoliths, and these magma source materials have previously been regarded as the determinant factor to the granite-related tungsten mineralization. Here we demonstrate, based on high Sr/Y and (La/Yb)N granites related to wolframite mineralization from the Jiaoxi, Jiaodong and Anglonggangri wolframite mining districts in the northern Lhasa terrane, Xizang that this viewpoint is not necessarily correct. Petrological and geochemical evidences suggest that the wolframite mineralization related granites in these mining areas were sourced from partial melting of the K-rich amphibolite lower crust of the Lhasa terrane and underwent significant fractional crystallization. These results indicate that the amphibolite lower crust can also be a candidate magma source for the GTD and the high evolution processes of granite is more important than the nature of the source materials during tungsten mineralization.

Reworking and maturation of continental crust in collision zones: Insights from Early Cretaceous compositionally diverse magmatic rocks in central Tibet

The reworking of continental crust in collision zones is a key process in the chemical maturation of crustal rocks. However, the mechanisms that cause crustal reworking remain highly controversial. The compositionally diverse magmatic rocks along the Lhasa–Qiangtang collision zone provide a favorable opportunity for studying the mechanism of crustal reworking and maturation in continental collision zones. Here we report zircon UPb ages and Hf isotopes, mineral major elements, and whole-rock geochemistry and SrNd isotopes for the Momu intrusive complex in the Lhasa–Qiangtang collision zone, central Tibet. Zircon UPb ages reveal that the intrusive complex formed during the late Early Cretaceous (115–113 Ma). Diorites from the intrusive complex have high Mg# values (49.7–51.2) and initial 87Sr/86Sr ratios (0.7082 to 0.7083), and low εNd(t) values (−7.3 to −6.9), with negative to slight positive zircon εHf(t) values (−3.8 to +0.8), suggesting that these rocks were likely generated by the partial melting of the enriched lithospheric mantle. Granodiorites from the intrusive complex have high SiO2 (64.4–67.9 wt%) and Al2O3 (14.8–16.1 wt%) and low MgO (1.4–1.8 wt%) contents. These rocks are also characterized by high initial 87Sr/86Sr ratios (0.7091–0.7098) and whole-rock negative εNd(t) (−9.9 to −8.4) and zircon εHf(t) (−7.9 to −2.2) values. The associated granites have the highest SiO2 (68.7–71.5 wt%) contents among the intrusive complex rocks, high initial 87Sr/86Sr (0.7089–0.7093) ratios, and negative whole-rock εNd(t) (−10.1 to −7.7) and zircon εHf(t) (−5.3 to −0.2) values. These geochemical characteristics indicate that the granodiorites were most likely derived from the partial melting of ancient continental crust and that the coeval granites were formed by the fractional crystallization of granodioritic magmas. Integrating our new results with data for the coeval magmatic rocks of the Lhasa–Qiangtang collision zone, we suggest that the Momu intrusive complex formed in a post-collisional slab breakoff setting. Asthenosphere upwelling caused by slab breakoff could have provided a substantial source of heat for crustal reworking, which gradually contributed to the maturation of continental crust in the Lhasa–Qiangtang collision zone.

Textures and Chemistry of Crystal Cargo of the Pleiades Volcanic Field, Antarctica: Potential Influence of Ice Load in Modulating the Plumbing System

Abstract The Pleiades Volcanic Field (PVF) of northern Victoria Land (Antarctica) is made up of a dozen scoria cones whose erupted products present an unusually complete evolutionary trend from alkali-basalt to trachyte. With the aim of reconstructing the evolution of the PVF plumbing system, we have investigated the petrography and chemistry of main mineral phases using scanning electron microscopy (SEM-EDS) coupled with major element analyses using an electron probe microanalyser (EPMA-WDS). We further focussed on clinopyroxene phenocrysts obtaining a more detailed characterization by means of trace laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) element analyses coupled with machine learning thermobarometry. The results indicate that fractional crystallization and magma mixing are the major processes determining the development of the complete evolution trend. While fractional crystallization is a persistently active process in all parts of the plumbing system, mixing among differently evolved magma batches pertaining to the same association is responsible for the formation of intermediate compositions in the differentiation lineage at a specific pressure range (0.4–0.5 GPa). These processes are compatible with significant residence time of magmas at depth, resulting in multiple episodes of magma mixing, as testified by resorption and overgrowth textures in phenocryst assemblage occurring under isobaric conditions. The prolonged residence time likely increased the efficiency of the mixing process, leading to the formation of magmas with intermediate composition. In turn, the build-up of volatiles during the magma differentiation at depth could have favoured the eruption of these (variably differentiated) magmas. Considering that the PVF is situated in a glacial region, a process forcing long magma residence time can be envisaged associated with increased ice loading during glacial stages. This study specifically considers the ice fluctuations in the last 100 ka, theorizing the possibility of a climate-controlled volcano plumbing system.

Platinum-Group Element Geochemistry of Igneous Rocks in the Chongjiang Cu–Mo–Au Deposit, Southern Tibet: Implications for the Formation of Post-Collisional Porphyry Cu Deposits

Abstract The timing and extent of sulfide saturation have been suggested as controlling factors in the formation of economically significant porphyry Cu deposits in subduction zone settings. However, details on the sulfide saturation history in post-collisional porphyry systems remain ambiguous. Accordingly, we have characterized the whole-rock geochemistry, including platinum-group elements (PGE), of igneous intrusions in the post-collisional Chongjiang porphyry Cu–Mo–Au deposit (southern Tibet) and utilize this data in conjunction with zircon U–Pb geochronological results and sulfide chemistry to assess the timing of sulfide saturation, the nature and amount of magmatic sulfide produced. The Chongjiang intrusions (monzogranite, biotite monzogranite porphyry, granodiorite, dacite porphyry, and quartz diorite porphyry) and mafic microgranular enclaves (MMEs) have zircon U–Pb ages of 14.2 to 12.8 Ma. Covariations in whole-rock major and trace elements among the Chongjiang intrusions and MMEs, together with similarities in their Sr–Nd and zircon Hf isotope compositions, indicate that they are co-magmatic and crystallized from a juvenile lower crustal melt that mixed with mafic melt derived from the lithospheric mantle; this hybrid melt subsequently evolved via fractional crystallization. Trace-element ratios in zircon and temperature − ∆FMQ estimates of the different intrusions suggest that they all crystallized from oxidized (average ∆FMQ = 1.9–2.6) and water-rich magmas. Palladium contents and Pd/Pt ratios in the Chongjiang igneous intrusions increase with decreasing MgO up to 3.9 wt % MgO, after which they abruptly decrease. The initial increase in Pd/Pt ratios likely results from the fractionation of a Pt-rich mineral (e.g. Pt–Fe alloy). The decrease in Pd contents and Pd/Pt ratios at 3.9 wt % MgO likely results from sulfide saturation during magma evolution, but prior to volatile exsolution, which occurred at approximately 1.4 to 2.4 wt % MgO. The presence of magmatic sulfide inclusions in amphibole and magnetite in samples with 3.9 wt % MgO, and the geochemical compositions of sulfide inclusions suggest that they represented trapped sulfide liquid and intermediate solid solution. Results of Monte Carlo simulations demonstrate that 0.003 to 0.009 wt % magmatic sulfide is required to have fractionated from the magma to explain the decrease in Pd contents at 3.9 wt % MgO. Highly chalcophile elements, such as Pd, will be sequestered by the magmatic sulfide that saturates at depth, decreasing their concentrations in the residual silicate melt, whereas concentrations of the less chalcophile elements, such as Cu, Mo, and even Au, will not be as significantly affected. Consequently, sufficient concentrations of Cu–Mo–Au will remain in the residual melt and, upon reaching volatile saturation, can be transported by the vapor phase to form porphyry Cu–Mo–Au deposits. In the case of the Chongjiang deposit, sulfide saturation was likely triggered by the high pressures and/or depletion of FeO caused by the thick (~70 km) crust beneath the Gangdese belt. This contribution presents evidence of sulfide saturation in post-collisional magmatic systems, and demonstrates that the amount of magmatic sulfide produced is a critical factor in controlling the formation of post-collisional porphyry Cu deposits.

Chemical Constituents, Hypolipidemic, and Hypoglycemic Activities of Edgeworthia gardneri Flowers.

The flowers of Edgeworthia gardneri are used as herbal tea and medicine to treat various metabolic diseases including hyperglycemia, hypertension, and hyperlipidemia. This paper investigate the chemical constituents and biological activities of ethanolic extract and its different fractions from E. gardneri flowers. Firstly, the E. gardneri flowers was extracted by ethanol-aqueous solution to obtain crude extract (CE), which was subsequently fractionated by different polar organic solution to yield precipitated crystal (PC), dichloromethane (DCF), ethyl acetate (EAF), n-butanol (n-BuF), and residue water (RWF) fractions. UHPLC-ESI-HRMS/MS analysis resulted in the identification of 25 compounds, and the main compounds were flavonoids and coumarins. The precipitated crystal fraction showed the highest phenolic and flavonoid contents with 344.4 ± 3.38mg GAE/g extract and 305.86 ± 0.87mg RE/g extract. The EAF had the strongest antioxidant capacity and inhibitory effect on α-glucosidase and pancreatic lipase with IC50 values of 126.459 ± 7.82 and 23.16 ± 0.79 µg/mL. Besides, both PC and EAF significantly regulated the glucose and lipid metabolism disorders by increasing glucose consumption and reducing TG levels in HepG2 cells. Molecular docking results suggested that kaempferol-3-O-glucoside and tiliroside had good binding ability with enzymes, indicating that they may be potential α-glucosidase and pancreatic lipase inhibitors. Therefore, the E. gardneri flowers could be served as a bioactive agent for the regulation of metabolic disorders.

In-vitro, in-vivo and in-silico anti-inflammatory evaluation of hedychenone and its semisynthetic derivative

Hedychium spicatum is a perennial shrub that is commonly found in the Himalayan region. Thin layer chromatography fingerprint screening of various Hedychium species revealed that only the species Hedychium spicatum possesses hedychenone. Purification and isolation of hedychenone was carried out from methanolic extract of Hedychium spicatum rhizomes powder using column chromatography. After crystallization of enriched fraction, 2.19% of hedychenone crystalline powder was yielded. The physiochemical, pharmacokinetic, and pharmacodynamic evaluation of the active pharmaceutical components was conducted using artificial learning and machine learning (AL/ML) approaches. The results indicate that both medications adhere to Lipinski’s rule of five. The docking study indicated that compound 2 (MBE-10.4 kcal/mol) exhibited a more sub-stantial interaction with the cannabinoid receptor 2 compared to hedychenone (MBE -9.85 kcal/mol). A study was done to assess the physical and chemical stability of hedychenone under biological pH conditions. Furthermore, the administration of both medication concentrations, 100 mg/kg and 200 mg/ kg, effectively inhibits the development of acute paw edema caused by ovalbumin. A preliminary investigation of hedychenone and its synthetic derivative indicated that these compounds have the potential to be utilized as active medicinal ingredients in herbal pharmaceutical preparations.

Magma Evolution During Main‐Phase Continental Flood Basalt Volcanism: A Case for Recharge‐Evacuation‐Assimilation‐Fractional Crystallization in the Ethiopian Low‐Ti Province

AbstractLavas erupted in Continental Flood Basalt (CFB) provinces are not primary magmas; they are differentiated products that result from large volumes of melt migrating and stalling in the lithosphere prior to eruption, resulting in complex liquid lines of descent. Geochemical models can be used to constrain the various influencers of magma differentiation (recharge, assimilation, fractional crystallization (FC), eruption, and mixing). Temporal constraints for changes in plumbing system dynamics are recorded in the petrography and stratigraphy of the erupted lava flows. This study focuses on the flow‐stratigraphy preserved within the Oligocene Ethiopian low‐Ti flood basalt province, located on the NW Ethiopian Plateau. We present new bulk rock geochemistry from 107 lavas and interpret these data within a petrostratigraphic framework. Our model results suggest that both a deep (∼0.6 GPa) and shallow (&lt;0.2 GPa) magmatic system are active throughout the main phase of volcanism. Our recharge evacuation assimilation and fractional crystallization models (REAFC) show that during the main phase of magmatism evacuation from both the deep (65%) and shallow (55%) systems reached an apex. During the terminal phases, magma evacuation from the deeper system ceases while evacuation from the shallow system is much reduced (25%). The degree of crustal contamination predicted by REAFC (4%–10%) is lower than previous estimates determined for this region using assimilation with FC only models (12%–25%). Our study highlights the importance of evaluating petrography while interpreting geochemical models in CFB.

Chemical evolution of major and minor minerals in rocks of the Arbarastakh complex (Aldan shield, Republic of Sakha, Yakutia)

The alkaline-ultrabasic carbonatite complex Arbarastakh is located in the southwestern part of the Siberian Craton. In addition to ultrabasic rocks such as pyroxenites and ijolites, various types of carbonatite dikes, phoscorites, and aillikites are present in the massif. Based on their modal and compositional characteristics, as well as the chemical composition of minerals, the rocks of the Arbarastakh complex have been divided into three groups: "aillikite", "phoscorite", and "alkaline-silicate and carbonatite" groups. The chemical compositions of olivines, phlogopites and spinellides indicate that aillikites are the least differentiated rocks in the complex. The compositional differences of micas from the "phoscorite" and "alkaline-silicate and carbonatite" groups support the liquation of the aillikite melt into two immiscible silicates and CPIO (carbonate-phosphate/iron-oxide-rich) melts. After liquation, for the "phoscorite" and "alkaline-silicate and carbonatite" groups, evolution follows fractional crystallization. Pyroxene-phlogopite-calcite and calcite carbonatites probably resulted from metasomatic alteration of silicate phases by apatite-dolomite carbonatites, which is confirmed by structural-textural features and the overlapping compositions of phlogopites, apatites and pyroxenes from calcite carbonatites and those from pyroxenites and ijolites.

Protracted and Progressive Crustal Melting during Continental Collision in the Pamir and Plateau Growth

Abstract Determining crustal melting in parallel with geodynamic evolution provides critical information on plateau crustal thickening and uplift. Here we investigate the timing and duration of crustal melting through in situ analysis of zircon U–Pb ages, trace elements and Hf–O isotopes, and whole-rock elements and Sr–Nd–Hf isotopes for the granites and high-grade metamorphic rocks from the Pamir Plateau. Zircon dates record protracted crustal melting for both Central Pamir (43–33 and 22–12 Ma) and South Pamir (28–10 Ma). The Pamir Cenozoic granites are characterized by significant elemental and isotopic heterogeneity. The elemental variability within the Pamir Cenozoic granites is dominantly attributed to fractional crystallization of K-feldspar and plagioclase with subordinate biotite from a variably fractionated melt, and the accumulation of early crystallized feldspar during magma ascent. Peritectic mineral entrainment and accessory mineral crystallization had some influence on the geochemical characteristics of the garnet-bearing leucogranite dikes. Zircon Hf isotopes and whole-rock Sr–Nd–Hf isotopes show secular variations for both Central and South Pamir granites. The Central Pamir granites show a mild decrease in whole-rock ƐNd(t) values from Eocene (−4.3 to −4.9) to Miocene (−6.2 to −7.7), and the zircon ƐHf(t) values decrease from c. 40 Ma (+2 to −5) to c. 10 Ma (−4 to −8). In contrast, the South Pamir granites have highly variable whole-rock Sr–Nd–Hf (87Sr/86Sr(i) = 0.7053 to 0.7830; ƐNd(t) = −31.5 to +0.2; ƐHf(t) = −40.0 to +8.2) and zircon Hf isotopes (ƐHf(t) = −31.7 to +7.5) and display a strong decrease in ƐNd(t) and ƐHf(t) values from c. 25 Ma to c. 13 Ma. Geochemical and isotopic data indicate that both the Central and South Pamir experienced crustal melting from juvenile lower crust to ancient lower-middle crustal materials, and Indian crustal materials were incorporated into the melt region of the South Pamir leucogranites from c. 20 Ma. Our study highlights a causal link between a chain of events that includes magma underplating induced by lithosphere thinning and slab breakoff, lithosphere delamination and underthrusting of Indian lithosphere, and formation of the Cenozoic granites in Pamir. This series of processes are incorporated here into a comprehensive model for the geodynamic evolution of the Pamir during the India–Asia collision.