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Abstract The 2021 La Palma eruption (Tajogaite) was unprecedented in magnitude, duration, and degree of monitoring compared to historical volcanism on La Palma. Here, we provide data on melt inclusions in samples from the beginning and end of the eruption to compare the utility of both melt and fluid inclusions as recorders of magma storage. We also investigated compositional heterogeneities within the magmatic plumbing system. We found two populations of olivine crystals: a low Mg# (78–82) population present at the beginning and end of eruption, recording the maximum volatile contents (2.5 wt % H₂O, 1,800 ppm F, 700 ppm Cl, 3,800 ppm S) and a higher Mg# (83–86) population sampled toward the end of the eruption, with lower volatile contents. Despite their host composition, melt inclusions share the same maximum range of CO₂concentrations (1.2–1.4 wt %), indicating olivine growth and inclusion capture at similar depths. Overall, both melt and fluid inclusions record similar pressures (450–850 MPa, ∼15–30 km), and when hosted in the same olivine crystal pressures are indistinguishable within error. At these mantle pressures, CO₂is expected to be an exsolved phase explaining the similar range of CO₂between the two samples, but other volatile species (F, Cl, S) behave incompatibly, and thus, the increase between the two olivine populations can be explained by fractional crystallization prior to eruption. Finally, based on our new data, we provide estimates on the total volatile emission of the eruption. 

Abstract Arc magmas are produced from the mantle wedge, with possible addition of fluids and melts derived from serpentinites and sediments in the subducting slab. Identification of various sources and their relevant contributions to such magmas is challenging; in particular, at continental arcs where crustal assimilation may overprint initial geochemical signatures. This study presents oxygen isotopic compositions of zoned olivine grains from post-caldera basalts and boron contents and isotopes of these basalts and glassy melt inclusions hosted in quartz and clinopyroxene of silicic tuffs in the Toba volcanic system, Indonesia. High-magnesian (≥87 mol% Fo [forsterite]) cores of olivine in the basalts have δ18O values ranging from 5.12‰ to 6.14‰, indicating that the mantle source underneath Toba is variably enriched in 18O. Olivine with <87 mol% Fo has highly variable (4.8–7.2‰), but overall increased, δ18O values, interpreted to reflect assimilation of high δ18O crustal materials during fractional crystallization. Mass balance calculations constrain the overall volume of crustal assimilation for the basalts as ≤13%. The processes responsible for the 18O-enriched basaltic melts are further constrained by boron data that indicate the addition of <0.1 wt% fluids to the mantle, >40% of the fluids being derived from serpentinites and others from altered oceanic crust and sediments. This amount of fluids can increase δ18O of the magma by only ~0.02‰. Approximately 6–9% sediment-derived melt hybridization in the mantle wedge is further needed to yield basaltic melts with δ18O values in equilibrium with those of the high-Fo olivine cores. The cogenetic silicic tuffs, on the other hand, seem to record a higher proportion of fluid addition dominated by sediment-derived fluids to the mantle source, in addition to crustal assimilation. Our reconnaissance study therefore demonstrates the application of combined B and O isotopes to differentiate between melts and fluids derived from serpentinites and sediments in the subducted slab—an application that can be applied to arc magmas worldwide. 

Abstract Coral strontium‐to‐calcium ratios (Sr/Ca) provide quantitative estimates of past sea surface temperatures (SST) that allow for the reconstruction of changes in the mean state and climate variations, such as the El Nino‐Southern Oscillation, through time. However, coral Sr/Ca ratios are highly susceptible to diagenesis, which can impart artifacts of 1–2°C that are typically on par with the tropical climate signals of interest. Microscale sampling via Secondary Ion Mass Spectrometry (SIMS) for the sampling of primary skeletal material in altered fossil corals, providing much‐needed checks on fossil coral Sr/Ca‐based paleotemperature estimates. In this study, we employ a set modern and fossil corals from Palmyra Atoll, in the central tropical Pacific, to quantify the accuracy and reproducibility of SIMS Sr/Ca analyses relative to bulk Sr/Ca analyses. In three overlapping modern coral samples, we reproduce bulk Sr/Ca estimates within ±0.3% (1σ). We demonstrate high fidelity between 3‐month smoothed SIMS coral Sr/Ca timeseries and SST (R = −0.5 to −0.8;p < 0.5). For lightly‐altered sections of a young fossil coral from the early‐20th century, SIMS Sr/Ca timeseries reproduce bulk Sr/Ca timeseries, in line with our results from modern corals. Across a moderately‐altered section of the same fossil coral, where diagenesis yields bulk Sr/Ca estimates that are 0.6 mmol too high (roughly equivalent to −6°C artifacts in SST), SIMS Sr/Ca timeseries track instrumental SST timeseries. We conclude that 3–4 SIMS analyses per month of coral growth can provide a much‐needed quantitative check on the accuracy of fossil coral Sr/Ca‐derived estimates of paleotemperature, even in moderately altered samples. 

Massif-type anorthosites, enormous and enigmatic plagioclase-rich cumulate intrusions emplaced into Earth’s crust, formed in large numbers only between 1 and 2 billion years ago. Conflicting hypotheses for massif-type anorthosite formation, including melting of upwelling mantle, lower crustal melting, and arc magmatism above subduction zones, have stymied consensus on what parental magmas crystallized the anorthosites and why the rocks are temporally restricted. Using B, O, Nd, and Sr isotope analyses, bulk chemistry, and petrogenetic modeling, we demonstrate that the magmas parental to the Marcy and Morin anorthosites, classic examples from North America’s Grenville orogen, require large input from mafic melts derived from slab-top altered oceanic crust. The anorthosites also record B isotopic signatures corresponding to other slab lithologies such as subducted abyssal serpentinite. We propose that anorthosite massifs formed underneath convergent continental margins wherein a subducted or subducting slab melted extensively and link massif-type anorthosite formation to Earth’s thermal and tectonic evolution. 

We present a new set of reference materials, the ND70‐series, forin situmeasurement of volatile elements (H₂O, CO₂, S, Cl, F) in silicate glass of basaltic composition. The materials were synthesised in piston cylinders at pressures of 1 to 1.5 GPa under volatile‐undersaturated conditions. They span mass fractions from 0 to 6%m/mH₂O, from 0 to 1.6%m/mCO₂and from 0 to 1%m/mS, Cl and F. The materials were characterised by elastic recoil detection analysis for H₂O, by nuclear reaction analysis for CO₂, by elemental analyser for CO₂, by Fourier transform infrared spectroscopy for H₂O and CO₂, by secondary ion mass spectrometry for H₂O, CO₂, S, Cl and F, and by electron probe microanalysis for CO₂, S, Cl and major elements. Comparison between expected and measured volatile amounts across techniques and institutions is excellent. It was found however that SIMS measurements of CO₂mass fractions using either Cs⁺or O⁻primary beams are strongly affected by the glass H₂O content. Reference materials have been made available to users at ion probe facilities in the US, Europe and Japan. Remaining reference materials are preserved at the Smithsonian National Museum of Natural History where they are freely available on loan to any researcher.