Geochemical Variations Research Articles

A spatio-temporal assessment of seawater quality in Miri-Sibuti Coral Reef: Evaluating for metal pollution, sources and dynamics

Coral environments are sensitive to seawater quality, and their sustenance depends on understanding the dynamics of geochemical variables, especially in trace levels. Miri-Sibuti Coral Reef National Park (MSCRNP) is a unique marine reserve in the state of Sarawak, NW Borneo, Malaysia, which attracts tourists worldwide. In this study, seawater samples were collected from MSCRNP in three different diving sites (Eve’s Garden (EG), Anemone Garden (AG) and North Siwa (NS)) at different depths for three seasons (pre-southwest monsoon (PRSWM), post-southwest monsoon (POSWM) and northeast monsoon (NEM). Insitu parameters (temperature, pH, salinity and turbidity) were measured in the field. The concentration of trace metals was determined in the water column (sea surface layer, middle layer and bottom water) using standard procedure. Statistics and pollution indices were used to identify the possible sources of metals and the pollution status of the seawater. From the analytical results, the vertical distribution of trace metal concentrations with respect to the locations and seasons was identified. pH ranging from 7.8 to 8.4 with a depth-wise increasing trend in NS during NEM. Similarly, a decreasing trend of turbidity was observed in AG and EG in all the seasons with respect to depth. A higher concentration of trace metals was observed during NEM, particularly at EG and NS. Fe, Ni and Pb are the dominant metals in all the seasons. Fe concentration varies from 789 to 1,478µg/L, averaging 1,112µg/L irrespective of seasons and locations. The suspended solids/sediments discharged by the river runoff were the main contributor to the distribution of metals. The release of metals from the suspended particles through desorption at the surface layers and the exchange of metals between water-sediment interface at the bottom water were observed. In addition, coastal development and other anthropogenic activities in this region were also contributed to the metal pollution.

Generation of Neoproterozoic granites of the Huangling batholith in the northern Yangtze Block, South China: Implications for the evolution of the Precambrian continental crust

Granites may contain critical information about composition and reworking of continental crust and are widely used to investigate continental crust evolution. Extensive Neoproterozoic granites in the northern Yangtze Block are significant to the Neoproterozoic continental evolution of the Yangtze Block. We investigated the petrology, mineralogy, whole-rock geochemistry, and zircon U–Pb–Hf isotopes of the Neoproterozoic Wuduhe biotite granites and Xiabaoping K-feldspar granites of the Huangling batholith in the northern Yangtze Block to determine their source characteristics and geological implications for the northern Yangtze Block. The Wuduhe biotite granites yielded zircon U–Pb ages of ca. 818–815 Ma. They displayed high SiO2 contents (70.19–74.23 wt%) and Na2O/K2O ratios (1.38–3.35) but low MgO (0.37–0.90 wt%) and CaO (1.49–2.97 wt%) contents, representing calc-alkaline Na-rich I-type granites. They exhibited enriched whole-rock εNd(t) (−19.8 to − 18.8) and zircon εHf(t) values (−41.3 to − 24.2), and had low CaO/Na2O (0.34–0.63), Al2O3/TiO2 (46.6–89.7), Rb/Ba (0.02–0.08), and Rb/Sr (0.04–0.12) ratios, as well as low zircon saturation temperatures (739 − 770 °C), indicating derivation from Na-rich metabasalts of the Archean Kongling complex. The Xiabaoping K-feldspar granites had zircon U − Pb crystallization ages of ca. 816–812 Ma. They displayed high SiO2 (70.82–74.80 wt%), K2O (4.41–6.35 wt%), and Al2O3 (13.46–16.31 wt%) contents, suggesting A2-type affinities. They showed enriched zircon εHf(t) (−44.3 to − 18.4) and whole-rock εNd(t) values (−23.4 to − 18.4) and high zircon saturation temperatures (869–912 °C), indicating formation by anhydrous melting of K-rich felsic rocks from the Archean Kongling complex. The geochemical diversity of these granites from the Huangling batholith was primarily controlled by source heterogeneity of the Kongling complex and distinct melting temperatures. We infer that the northern Yangtze Block underwent significant remelting of ancient continental crust in a subduction background during the Neoproterozoic, induced by continuous upwelling of mantle-derived mafic magmas.

Underplating-induced trans-crustal melting and maturation of Neoarchean continental crust in the North China Craton

A global change in granitoid compositions from early predominantly sodic tonalite-trondhjemite-granodiorites (TTGs) to later TTGs and more potassic granites occurred during the late Archean, coupled with a major period of crustal maturation. However, the detailed relationship between granitoid chemical evolution and the maturing crustal process remains enigmatic. Successive granitoid magmatism including late Neoarchean TTGs and high-K granites occurred in the Western Shandong Province granite-greenstone belt (WSP) of the North China Craton and thus preserves crucial clues of the crustal maturation process. In this study, petrology, whole-rock geochemistry, and zircon U-Pb and Lu-Hf isotopes are reported for the late Neoarchean TTG gneisses, monzogranites, and minor metabasaltic to andesitic rocks from the WSP. The ca. 2560−2540 Ma TTG gneisses show low MgO, K2O/Na2O, but high (La/Yb)N, Sr/Y, and absence of Eu anomalies, indicating their derivation from partial melting of the thickened lower mafic crust. The ca. 2530−2500 Ma monzogranites are characterized by systematically high SiO2 and K2O/Na2O, but low MgO and Sr/Y, and moderately negative Eu anomalies, revealing they were formed by intracrustal reworking of local TTGs and sedimentary rocks in the middle to upper crust. Geochemical variations of these crustal-derived granitoids suggest that they were formed by melting at gradually higher crustal levels with the melt zone moved gradationally from the eclogite stability field into the plagioclase stability field. The ca. 2530−2500 Ma calc-alkaline metabasaltic to andesitic rocks sourced from metasomatized mantle outline roles of mantle-derived magma underplating in contributions of heating and trans-crustal melting magmatism. The long-term melting processes facilitated the upward movement of volatiles and heat-producing elements from deep to shallow crustal levels, and introduced K-enriched monzogranites into the upper crust, leaving a refractory, strengthening, and tectonically stable lower crust. Secular compositional evolution of crustal-derived granitoids reveals that continuous crustal reworking drove lithosphere differentiation and paved the way for the maturation of the Archean continental crust.

Rubidium (Rb) enrichment processes in a highly evolved granitic system: Insights from the petrology and geochemistry of the Guobaoshan Rb deposit in eastern Tianshan, NW China

Highly fractionated granitoids are closely associated with Rb mineralization, yet the mechanisms that control Rb enrichment and details about the enrichment process have not been well constrained. The Guobaoshan Rb deposit in eastern Tianshan, NW China, is one of the largest granite-related Rb deposits; it preserves a series of gradual lithofacies ranging from biotite granite and muscovite granite to Rb-rich amazonite granite and pegmatite, and provides an excellent opportunity to constrain the Rb enrichment processes in granitic systems. The large Guobaoshan Rb deposit hosts 281,000 tons of Rb2O at a grade of 0.12% mainly in its amazonite-bearing granite and amazonite granite lithofacies. In this contribution, we integrate geochronology, bulk-rock geochemistry, and analysis of Nd and zircon Hf isotopes to characterize the evolution of the Guobaoshan granitic pluton and the mechanisms that generated Rb enrichment. The zircon U-Pb age of the biotite granite and columbite U-Pb age of the amazonite granite are 244.8 ± 1.8 Ma (1σ, mean square of weighted deviates [MSWD] = 1.1) and 241.9 ± 2.3 Ma (1σ, MSWD = 1.0), respectively. In situ Rb-Sr analysis of orthoclase, mica, and albite from the amazonite-bearing granite, amazonite granite, and pegmatite yields ages of 249.1 ± 7.3 Ma (2σ, MSWD = 1.6), 245.5 ± 16.8 Ma (2σ, MSWD = 0.63), and 245.8 ± 9.8 Ma (2σ, MSWD = 3.3), respectively. Together, these ages demonstrate that the Guobaoshan granitic pluton formed during the Triassic and underwent a protracted magmatic evolution. The Guobaoshan granitic pluton is characterized by high concentrations of SiO2, alkalis, and Al2O3, and low concentrations of MgO, Fe2O3, CaO, P2O5, and TiO2, with an Al saturation index (A/CNK) of 1.01−1.14. It is enriched in Rb, but depleted in Ba, Sr, P, and Eu, has low total rare earth element (REE) contents (83.1−221 ppm), and is characterized by significantly negative anomalies (Eu/Eu* = 0.01−0.44). The biotite granite is enriched in light rare earth elements (LREEs), whereas the muscovite granite, amazonite-bearing granite, amazonite granite, and pegmatite are depleted in LREEs, and exhibit a marked tetrad effect (TE1.3 = 1.05−1.50). These geochemical characteristics, combined with the non-CHARAC (charge-radius−controlled) ratios of Zr/Hf, Nb/Ta, Y/Ho, and K/Rb, are indicative of melt-fluid interaction during the evolution of the Guobaoshan magma. Given that the biotite granite is the least-evolved rock, its petrological and geochemical characteristics suggest that it is an I-type granite. The slightly variable εHf(t) and consistently negative εNd(t) values indicate that the magma from which the Guobaoshan granitic pluton crystallized was likely sourced from the Mesoproterozoic crust, with limited mantle contributions. The coeval ages and coherent geochemical variations and mineral compositions of these rocks suggest that they formed via fractional crystallization of plagioclase, mica, quartz, and K-feldspar in the same magmatic system. This is supported by fractional crystallization simulations using the rhyolite-MELTS software package. Based on the petrological, mineralogical, and geochemical characteristics of the muscovite granite, amazonite-bearing granite, amazonite granite, and pegmatite, as well as simulations using rhyolite-MELTS, high degrees of fractional crystallization of granitic magma and interaction of this evolving magma with F-rich fluids are suggested to have been the key mechanisms that caused enrichment of Rb, while the melt-fluid interaction was more critical for Rb mineralization.

A dynamic mid-crustal magma domain revealed by the 2023 to 2024 Sundhnúksgígar eruptions in Iceland.

Mid-crustal magma domains are the source of many basaltic eruptions. Lavas from individual eruptions are often chemically homogeneous, suggesting that they derive from single, well-mixed magma reservoirs. The 2023 to 2024 eruptions at Sundhnúksgígar in the Svartsengi volcanic system in Iceland provide an opportunity to observe the behavior of a mid-crustal magma domain at high spatial and temporal resolution by detailed sampling and geochemical characterization. We observed substantial mantle-derived geochemical variability in the products erupted in the first hours of the December 2023 and January, February, and March to May 2024 eruptions, indicating that the eruptions derived from multiple magma reservoirs, which mineral-melt equilibration pressures place in the mid crust. The unusual presence of geochemical heterogeneity in the mid-crustal magma domain provides insights into how dynamic and complex mid-crustal magma domains can be.

Ridgeward flow of compositionally heterogeneous mantle produces near-ridge seamount chains in the South Pacific

Many near-ridge seamounts and seamount chains in the Pacific Ocean have a nonplume origin. Yet, their origin remains to be fully understood. Our new geochemical study on seamount basalts from the Pukapuka Ridge (PPR) finds a large along-ridge lava compositional variation with a gradual decrease in a geochemically enriched component toward the East Pacific Rise (EPR) axis. This spatial geochemical variation is best understood as resulting from decompression melting of compositionally heterogeneous mantle flowing toward the ridge, where the mantle consists of low-solidus materials of metasomatic origin dispersed within a more refractory peridotite matrix. Far from the ridge axis, preferential melting of enriched lower-solidus materials under thicker lithosphere leaves less enriched residues that undergo further decompression melting as they flow beneath thinner lithosphere toward the ridge axis. This process gives rise to the progressively less enriched lavas along the PPR chain toward the EPR. The residual enriched mantle component became embedded in the mantle beneath the southern EPR (13°S−23°S), forming an along-axis compositional dome at the EPR-PPR intersection (∼17°S−19°S). We predict that nonplume seamounts are best expressed as linear chains near and perpendicular to ocean ridges on fast-spreading plates as long as the flowing mantle is sufficiently heterogeneous. This finding explains widespread seamounts of nonplume origin in the Pacific Ocean, and it also explains the geophysical asymmetries in the mantle electromagnetic tomography (MELT) area.

Li enrichment in peridotites and chromitites tracks mantle-crust interaction

The ultramafic massifs of the Serranía de Ronda in southern Spain are the Earth's largest exposures of subcontinental lithospheric mantle (SCLM) peridotites (∼450 km2). These ultramafic massifs experienced asthenosphere melt percolation during their crustal emplacement. Mixing of these mafic melts with anatectic melts and fluids led to the formation of a world's unique Ni-arsenide-rich chromitite ores (hereafter CrNi ores) associated with orthopyroxenite and/or cordieritite (i.e., > 90 % volume of cordierite) hosted within the peridotites. This study uses laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to investigate the Li in rock-forming minerals of peridotite and CrNi ores to evaluate the role of Li as crustal tracer. Clinopyroxene crystallized from asthenospheric melts exhibits high Li contents (up to 8.5 ppm), exceeding the average values of the upper mantle (∼ 0.7 ppm), whereas orthopyroxene, olivine, and Cr-spinel from peridotite are mostly Li-depleted. In contrast, all rock-forming minerals of CrNi ores have abnormally high Li contents, displaying an overall Li enrichment trend toward the external parts of ultramafic massifs, on the way to the crustal rocks. This trend is evident in Cr-spinel from the CrNi ores, which display 6.9–7.9 ppm Li in the deepest portions of the massif (Arroyo de la Cala CrNi ore) up to 1.4–8.5 ppm in the shallowest part (La Gallega CrNi ore), as well as in orthopyroxenes that have 31.3–44.7 ppm Li in Arroyo de la Cala, and 45.1–51.4 ppm Li in La Gallega. Cordierite is present only in the CrNi ores situated in the external part of the ultramafic massifs, exhibiting 113.15–160.82 ppm Li in the Barranco de las Acedías CrNi ore and 36.5–60.5 ppm Li in La Gallega CrNi ore. Similarly to Li, LREE, fluid-mobile elements (K, Rb, Ba), and Sr in orthopyroxenes from the CrNi ores display enrichment from the inner to the outer parts of the ultramafic massif. These geochemical variations suggest that Li enrichment in CrNi ores and host peridotites was a twofold process: (1) asthenospheric melt percolation slightly increased Li abundances in the SCLM peridotites by modal and cryptic metasomatism involving clinopyroxene; (2) additional infiltration of Li-bearing crustally-derived fluids during the intracrustal emplacement of the mantle section boosted the Li contents of minerals in the CrNi ores. Our results highlight that Li may effectively track the interaction of the SCLM with crustal components.

High resolution paleo-hydrological record from carbonate deposits in the Roman aqueduct of Traconnade (Aix-en-Provence, SE France)

Carbonate deposits in aqueducts are potential valuable archives of the paleo-hydrological record for the Roman period. Here we present a new high-resolution record from carbonate deposits in the aqueduct of Traconnade built for Aix-en-Provence, the Roman city of Aquae Sextiae. As its name indicates, Aquae Sextiae was built around an abundant source of water but its development, like other ancient cities, required good management of this resource. Through a combination of micromilling and in situ analysis (LA–MC–ICPMS) on thin sections, we measured geochemical variations (stable isotopes and trace elements) and performed sampling for absolute UTh dating. Geochronological results based on classical correction and isochron along with archaeological observations confirm that the carbonate concretion was deposited in Roman times on the walls of the Traconnade aqueduct, built no later than 140 CE. Carbonate δ18O records document the presence of clear geochemical cycles that were mainly controlled by seasonal variations in temperature and δ18O from water circulating in the aqueduct. Minima and maxima in δ18O values were attributed to summer and winter conditions, respectively in agreement with the modern spring’s stable isotope values. The other tracers (Mg/Ca, Sr/Ca and δ13C) also show marked cyclicities with maximum values occurring in summer. The enrichment in trace elements and δ13C were linked to processes occurring during dry periods (1) prior precipitation of calcite in the epikarst, and/or (2) a greater degree of CO2 degassing. The geochemical variations in Ba/Ca, U/Ca and Rb/Ca behave differently and their co-variations may reflect the water-rock interactions in the karst system. We highlight that these tracers can be used as a proxy for intense precipitation events, occurring frequently during autumn. The Traconnade aqueduct carbonate provides sufficient temporal resolution to explore environmental variations on a seasonal scale. These results suggest the occurrence of a double rainy season (spring and autumn) in the Aix-en-Provence region, similar to present-day climatic conditions. Our study confirms the high potential of aqueduct concretions for paleohydrological studies.

Provenance and depositional environment of the Mbam River overbank clay deposits, Central Africa: evidence from mineralogical and geochemical variations

Provenance and depositional environment of the Mbam River overbank clay deposits, Central Africa: evidence from mineralogical and geochemical variations

Geochemical fingerprinting of Norway spruce from the Eastern Carpathians: Sr isotopic and multi-elemental signatures

Ensuring efficient wood traceability within procurement chains is essential for establishing sustainable forest management and minimizing environmental damage in countries that produce and export timber. While some progress has been made with key legislative reforms to tackle this issue, the effectiveness of law enforcement still relies on the availability of appropriate analytical tools to determine the provenance of wood. This study documents the Sr isotopic and multi-elemental signatures of Norway spruce trees in the Eastern Carpathians, Romania – an area known for intensive forest logging. The research focused on trees from Rodna, Rarău, and Călimani, analyzing tree rings from 1970 to 2020 to assess temporal variability and develop site-specific geochemical fingerprints. In conjunction with tree samples, corresponding soil, groundwater, and river samples were analyzed, providing a comprehensive view of the bioavailable 87Sr/86Sr ratios in these ecosystems. The study found a strong correlation between the Sr isotope ratios in the wood and those in corresponding water and soil samples, confirming that the wood accurately mirrors local geochemical signatures. The Sr isotope ratios were consistent across most of the cores from trees within the same site but varied among sites within the same region. Principal Component Analysis of the Sr isotopic and multi-elemental data highlighted closer clustering of samples from the Călimani area, though distinguishing the samples from the Rodna and Rarău regions proved more difficult due to overlapping data points. This study broadens our understanding of geochemical variability and its implications. The insights gained provide a valuable foundation for future research aimed at enhancing wood traceability methods.

Petrogenesis of magmatic charnockite-biotite granite suite from parts of the Chotanagpur Granite Gneissic Complex (CGGC), eastern Indian shield: Implication for the break down of the Columbia Supercontinent

A rare porphyritic charnockite that is girdled by and mineralogically grades to biotite granite occurs as a part of the Chotanagpur Granite Gneissic Complex (CGGC) in and around Massanjore, Jharkhand, India. Preservation of certain textural features, including (a) euhedral to subhedral grains of orthopyroxene, (b) low dihedral angle subtended by orthopyroxene and plagioclase grains, and (c) relict intergranular and porphyritic textures, are consistent with the view that orthopyroxene in the studied rocks has a magmatic origin. Preserved magmatic features and other petrological attributes of these rocks do not support any significant mass change beyond a few tens of microns during the overprinting high-grade metamorphism. The geochemical variation of the felsic rock suite (porphyritic charnockite and biotite granite) indicates that they are cogenetic and are derived from a ferroan A-type granitoid magma by crystal fractionation. The observed geochemical trend of the studied felsic rock suites has been simulated by phase equilibria modelling in the open system using the system components Na2O-CaO-K2O-FeO-MgO-Al2O3-SiO2-H2O-TiO2-O2. The observed mineralogical and geochemical attributes and the results of the modelling study are consistent with a petrogenetic process in which high magma temperature (> 900 °C), low pressure, and low water activity in the parental melt favoured the separation of an orthopyroxene bearing cumulate assemblage (orthopyroxene + plagioclase + quartz + K-feldspar + ilmenite + magnetite) in the initial part of the magmatic differentiation. Removal of this anhydrous cumulitic assemblage raised the bulk H2O content in the residual melt. Orthopyroxene became unstable with respect to biotite in the evolved melt that eventually crystallised minerals that formed the biotite granite. An increase in magma fO2 also restricts the orthopyroxene stability in felsic magma. Taken together all the petrological and geochemical attributes, we demonstrate that fractionation of an orthopyroxene-bearing crystal cumulate from the melt is essential to form the charnockites, and that the biotite granite forms from the evolved melt after the fractionation. The charnockite-biotite granite association of the studied area was formed in an extensional tectonic setting, presumably during the breakdown of the Columbia Supercontinent.

Miocene magmatism in Northern Tunisia and its geodynamic implications

The Nefza igneous rocks in Northern Tunisia belong to the Miocene magmatic belt extending from Northern Tunisia to Morocco and consist mainly of Serravallian–Tortonian granodiorite and rhyodacite (~ 14–8 Ma) and Messinian basalts (~ 8–6 Ma). Differences in geochemical composition between units have been interpreted to be the result of geodynamic processes in the upper mantle below the Western Mediterranean area, but their implications for Northern Tunisia are unclear due to limited data. In this contribution, we present an updated geodynamic model for Northern Tunisia based on new petrographic and whole-rock geochemical results from the Nefza magmatic suite from outcrop and OB45 drill core samples. Petrographic observations show that rhyodacites display a microlithic texture with quartz, plagioclase, K-feldspar, biotite, and glass, whilst granodiorite contains plagioclase, quartz and exhibits fine-grained texture with a 2–3 mm crystal size. The Nefza magmatic rocks are overprinted by multiple weathering and alteration processes with loss of ignition (LOI) ranging between 0.88 and more than 5 wt%. The linear relationships between mobile elements (Ca, Na, P, K, Mg, Si), large-ion lithophile elements (LILE), and LOI suggest element mobilisation during alteration. Major and trace element compositions show the Nefza magmatic rocks plot in the rhyolite, dacite, and trachydacite fields for felsic rocks and plot in the basalt and trachybasalt fields for mafic rocks. Granodiorite and rhyodacite rocks exhibit negative Eu anomalies and a LILE enrichment (Rb, Ba, Pb) relative to high-field-strength elements (HFSE: Nb, Ta, Hf, Zr, REE). Mafic rocks enriched in LILE show geochemical characteristics between calc-alkaline and alkaline trends. Comparison with nearby regions suggests that the generation of calc-alkaline magmas resulted from the partial melting of the lithospheric mantle due to slab break-off or tearing in Eastern Algeria. The upward flow of asthenospheric material through the widening tear in the sinking slab leads to partial melting of the mantle and shallowing of the lithosphere–asthenosphere boundary, ultimately leading to the formation of alkaline magma. The Nefza geochemical variations underscore Mediterranean upper mantle heterogeneity, offering crucial insights into Mediterranean geodynamics. More studies are needed to constrain mantle dynamics and the region’s complex geological history.

Isotopic and trace element record of changing metal source contributions to tropical freshwater Lake Naivasha (Kenya)

Lake Naivasha, Kenya's second-largest freshwater body is a wetland of international ecological importance and currently subjected to unprecedented anthropogenic influence. The study aims to chronologically reconstruct the main human activities and background weathering reactions that govern metal mobilizations into the lake and their potentially adverse effects on its ecological status. We combine extensive geochemical analyses (major, trace elements, Zn-Pb isotope ratios) in a dated lake sediment record and catchment rocks with remote sensing techniques. Downcore geochemical variations reflect natural ecosystem destabilizations occurring as early as the first half of the 20th century. These coincide with changes towards less radiogenic Pb-isotope values which persist towards the top of the core (206Pb/207Pb = 1.243 at core base ∼1843, to 206Pb/207Pb = 1.225 at ∼1978). We interpret the land-clearance for agricultural purposes on the Aberdare Range and documented early aviation activities as possible vectors of this early Pb-isotope excursion. The overlapping Pb-isotope signatures between sediment sources and anthropogenic contributions challenges a straightforward deconvolution of the two. Our conservative model calculations suggest, nevertheless, that an addition of up to ∼1.8 % Pb-gasoline influx to the total Pb flux, peaking in the 1980s is able to explain the Pb distribution trend. Homogeneous Zn-isotope compositions in sediments deposited until ∼1970s (δ66/64Zn = 0.216–0.225 ‰) do not follow major hydro-climatic events or anthropogenic forcing but likely reflect lake-specific natural cycling. Subsequent higher variations to both heavier (up to δ66/64Zn = 0.242 ± 0.005 ‰) and lighter (down to δ66/64Zn = 0.184 ± 0.003 ‰) Zn-isotope values are contemporaneous with intensification of large-scale horticultural industry in the catchment. Together with supporting indicators, the lighter Zn-isotope compositions in youngest analysed sediments (21st century) are attributable to increased biological productivity (algal blooms) and ongoing lake eutrophication. Our study demonstrates the applicability of the heavy metal isotope tool to reconstruct human influences on lake environments with complex geological settings such as the East African Rift System.

Potassium isotope compositions of Mariana arc lavas and their sedimentary input

We apply the stable potassium isotope system (41K/39K) to well-studied Mariana arc lavas, in which inter-island geochemical variability has been interpreted to reflect near constant addition of an aqueous fluid flux, that dominantly samples the subducting mafic oceanic crust and variable amounts of sediment melt addition to the sub-arc mantle wedge. The nature of the sediment component in the Mariana arc lavas remains enigmatic, with a mixture of melts from all subducted sediment lithologies and the altered-mafic oceanic crust seeming likely, but some interpretations point towards a component from melting of the volcaniclastic sediment alone. We present K isotopic data on a set of well-characterised Mariana arc lavas and sediment samples (from Ocean Drilling Program site 801). Our data show that the majority of Mariana arc lavas are isotopically heavy (ẟ41K), by up to ∼0.2 ‰, relative to mid-ocean ridge basalt (MORB), but most of the subducting sediment samples are slightly isotopically lighter than, or indistinguishable from MORB. The volumetrically important volcaniclastic sedimentary unit however is significantly isotopically lighter than MORB, by ∼0.8 ‰, which reflects marine diagenetic processes. Thus, volcaniclastic material significantly influences the bulk sediment K isotope composition. We show that ẟ41K compositions of the Mariana arc lavas can be reproduced by the addition of an aqueous fluid with isotopically heavy K (relative to MORB) and an additional fraction of an incompatible-element-enriched isotopically light melt component. Modelling of K isotopes together with K/La and radiogenic Nd indicate that the melt component is best explained by a mix of melts from bulk sediment and altered-mafic oceanic crust. Our results show that distinctive K isotopic variations in subduction zone inputs and K isotopic fractionation during dehydration reactions makes K a useful tracer of subduction zone processes.

Geochemistry of Olivine Melt Inclusion Reveals Interactions Between Deeply Derived Carbonated Melts From the Big Mantle Wedge and Pyroxenite in the Lithospheric Mantle Beneath Eastern Asia

AbstractOur current knowledge regarding the distribution patterns of ancient and recent recycled materials, as well as the origin of intraplate basalts in the eastern Asia Big Mantle Wedge (BMW), is limited. To address this, we conducted a detailed geochemical analysis of olivine melt inclusions (OLMI) in nephelinite samples. The normal OLMIs detected in our investigation exhibit geochemical features that closely resemble those of the hosting nephelinite, indicating a consistent association with a carbonated mantle source. Additionally, we identified a distinct group of anomalous OLMIs that displayed different geochemical characteristics from the hosting nephelinite but showed similarities to regional alkali basalts sourced from pyroxenite. The observed geochemical diversity in the nephelinite OLMIs suggests an interaction between deeply derived carbonated melts originating from the flattened Pacific slab in the mantle transition zone and pyroxenite in the lithospheric mantle. Carbonated fluid‐fluxed melting is key to basalt formation in the BMW.

Examining the distribution of Middle Paleolithic Nubian cores relative to chert quality in southern (Nejd, Dhofar) and south‐central (Duqm, Al Wusta) Oman

AbstractLithic raw material properties are often invoked to explain the presence, absence, form, or ontogeny of Paleolithic stone tools. Here, we explore whether the frequency of the Middle Paleolithic Nubian core form and core‐reduction systems co‐varies with toolstone quality in two neighboring regions in Oman: the southern region of Nejd, Dhofar, and the south‐central region of Duqm, Al Wusta. Specifically, we predicted that if raw material differences were influencing the distribution of Nubian cores, the chert would be of higher quality in the southern region, where Nubian cores were frequent, and of lower quality in the south‐central region, where they were scarce. We tested this prediction by collecting 124 chert samples from 22 outcrops and then quantitatively assessed two geochemical variables that are widely thought to influence knapping: impurity amount and silica content. We also examined the mineralogical composition, and the crystallite size and lattice strain for quartz (crystalline α‐SiO2) of representative chert samples. Our results suggest that the cherts in the two regions are similar, which is not consistent with the hypothesis that lithic raw material quality contributed to Nubian core spatial distribution in Oman. We discuss potential alternative hypotheses to explain Nubian core geographic patterning, and provisionally suggest that the scarcity of Nubian cores in south‐central Oman may be due to a concomitant scarcity of toolmakers, given a lack of water availability.

Differences of soil carbon pools and crop growth across different typical agricultural fields in China: The role of geochemistry and climate change

Carbon storage and the aboveground biomass of farmland provide practical significance for understanding global changes and ensuring food production and quality. Based on soil carbon storage, aboveground biomass, climate, geochemistry, and other data from 19 farmland ecological stations in China, we analysed the distribution characteristics of farmland carbon storage in topsoil and aboveground biomass. We notably revealed the response direction and degree of climate and geochemical factors to farmland carbon storage in topsoil and aboveground biomass. The results indicated that the average carbon stocks of farmland in different regions ranged from 0.28 to 7.91 kg m−2, the average fresh weight of the aboveground biomass (FAB) ranged from 1370.64 to 5997.28 g m−2, and the average dry weight of the aboveground biomass (DAB) ranged from 119.95 to 852.35 g m−2. The least angle regression (LARS) and the best subsection selection regression (BSS) showed that evapotranspiration and extreme low temperatures were significant climatic factors affecting carbon sequestration and aboveground biomass on long-time scales. The linear mixed-effects model (LMM) further showed that AN and AP had significant long-term effects on carbon sequestration and aboveground biomass (p < 0.05), with AN having the highest contribution to SOC%, FAB, and DAB. The structural equation model (SEM) showed that carbon sequestration and aboveground biomass in agricultural fields were significantly positively correlated (p < 0.05). Moreover, the climate had a less direct contribution to carbon sequestration and above-ground biomass compared to geochemistry (PCc < 0.1<PCG), and its effect was more indirect. When the geochemical variables were removed, the correlation between climate and carbon and aboveground biomass variables decreased significantly. We conclude that it is possible that extremes climate and geochemistry control carbon sequestration and above-ground biomass in long-term cropland through interactions in the context of global change, which provides new insights into the evolution of soil organic carbon in long-term cropland and the scientific formulation of policies to increase food production and preserve quality.

Spatial and temporal evolution of magmatic arcs: Geochemical diversity and tectonic controls

We review the main petrologic and geochemical features of magmatic rocks from continental arcs compared to their intra-oceanic equivalents. Both types share a number of characteristics, including their typical HFSE-depleted incompatible element patterns and isotopic Sr, Nd, Pb and Hf features, intermediate between those of N-MORB and continental crust. They are thought to derive from the partial melting of the mantle wedge metasomatized by fluids emanating from the downgoing plate. They are dominantly hydrous fluids provided by the breakdown of amphibolites and antigorite serpentinites, but a significant role is attributed to felsic hydrous melts derived from oceanic metabasalts and associated sediments. The more enriched character of magmas from continental arcs with respect to those from intra-oceanic arcs is ascribed to their genesis from a less depleted mantle wedge in a milder thermal regime, to the enrichment of their source via subduction erosion of the continental margin, and finally to their contamination during ascent and storage within a thicker crust.

Microscale geochemical variations in metamorphic-hydrothermal scheelite and insights into trace element sources (Otago Schist, New Zealand)

ABSTRACT Scheelite (CaWO4) trace elements are frequently used to fingerprint sources of mineralising fluids or styles of mineralisation. However, the chemistries of scheelite from hydrothermal-metamorphic Otago Schist scheelite-quartz veins have complicated parageneses. Coarse (>1 cm) single grains from three deposits contain zones that fluoresce orange or blue in cathodoluminescence. Laser ablation analysis shows the orange zones to be richer in REE but the blue zones to be richer in Sr. With one exception, which may be due to incorporation of calcite, the internally homogenous in-situ 87Sr/86Sr and low Rb/Sr indicate isotopic equilibrium at the time of scheelite precipitation. Micro-drilled cores extracted, dissolved and measured for trace elements and 143Nd/144Nd isotopic compositions, together with the ingrowth history of 87Sr/86Sr and 143Nd/144Nd in the deposit host rocks, indicate that the scheelite isotopic ratios have distal or multiple sources to the Sr and Nd. Other trace elements therefore also likely have complicated paragenetic histories, which mean that these do not necessarily indicate either the element source or the style of mineralisation. A positive aspect is that the internal Sm/Nd variation means that single-grain isochrons resolve ages of 114 ± 50 Ma (Alta Lode) and 136 ± 45 Ma (Macraes) that overlap published ages.

Geochemical characteristics of peridotite xenoliths from the Vitim volcanic field: Insight to late Cenozoic mantle upwelling in SE Siberia

The Vitim volcanic field, comprising Cenozoic basaltic lava flows associated with the Baikal Rift volcanism, contains abundant mantle xenoliths that offer insights into the subcontinental lithospheric mantle (SCLM) beneath the region. This study investigates the mineralogical and geochemical compositions of these mantle xenoliths, entrained in Miocene and Pleistocene basalts. The xenoliths, predominantly garnet-, spinel-, and garnet-spinel-bearing lherzolites, exhibit high modal content of clinopyroxene and low fosterite content of olivine, suggesting a relatively fertile SCLM. Distinct variations in CaO and Al2O3 observed in spongy rims and cores of clinopyroxenes likely result from decompression-induced partial melting. Trace element patterns of clinopyroxene reveal three types: light rare-earth elements (LREE) depleted, LREE enriched, and transitional LREE types. Whole-rock trace element compositions of the four Vitim lherzolites showing flat to LREE and large ion lithophile elements enrichments are entirely consistent with those of their clinopyroxenes. The LREE depleted type indicates that these lherzolites were residual mantle after melt extraction, whereas the LREE enriched type suggests that they were metasomatized after residual mantle formed by partial melting. The transitional LREE type showing in-between features among the above two end-members could represent that those lherzolite underwent less or incomplete metasomatism, thus clinopyroxene cores still retain primary depleted LREE type feature of residual mantle. Most Vitim lherzolites were affected by cryptic metasomatism with less stealth metasomatism, whereas only those with secondary amphibole and apatite could be influenced by modal metasomatism. The lithospheric mantle beath the Vitim volcanic field representing by these lherzolites was metasomatized predominantly by hydrous fluids with minor silicate melts. Using the clinopyroxene melting model, it was found that most Vitim lherzolites have experienced <10% partial melting. Geothermal gradients estimated from mineral geothermobarometry indicate that lherzolites in the Pleistocene basalts equilibrated at shallower depths with higher temperatures compared to those in the Miocene basalts with deeper depths and lower temperatures. SrNd isotopic ratios, combined with previous results (Ionov et al., 2005), demonstrate that the Miocene lherzolites have a broader range from depleted to enriched components, whereas lherzolites in the Pleistocene basalts show lesser enrichment. It is proposed that the Pleistocene basalts captured shallower SCLM lherzolites experienced less degrees of melt metasomatism than those deeper SCLM lherzolites hosted by Miocene basalts. Considering the deeper SCLM is more vulnerable to metasomatism by ascending melts, such temporal and geochemical variation further emphasizes progressive asthenosphere upwelling beneath the Vitim region from the Miocene to Pleistocene time.