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Hydrogen (H$_{2}$) and hydrogen sulphide (H$_{2}$S) are typically present at only minor to trace levels in volcanic gas emissions, and yet they occupy a key role in volcanic degassing research in view of the control they exert on volcanic gas reducing capacity (e.g., their ability to remove atmospheric O$_{2}$). In combination with other major compounds, H$_{2}$ and H$_{2}$S are also key to extracting information on source magma conditions (temperature and redox) from observed magmatic gas compositions. Here, we use a catalogue, compiled by extracting from the geological literature a selection of representative analyses of magmatic to mixed (magmatic–hydrothermal) gases, to review the processes that control H$_{2}$ and H$_{2}$S abundance in volcanic gases. We show that H$_{2}$ concentrations and H$_{2}$/H$_{2}$O ratios in volcanic gases both exhibit strong positive temperature dependences, while H$_{2}$S concentrations and H$_{2}$S/SO$_{2}$ ratios are temperature insensitive overall. The high H$_{2}$ concentrations (and low H$_{2}$S/SO$_{2}$ compositions, of ${\sim }$0.1 on average) in high-temperature (${>}$1000 °C) magmatic gases are overall consistent with those predicted thermodynamically assuming external redox buffering operated by the coexisting silicate melt, at oxygen fugacities ranging from ${\Delta }$FMQ $-$1 to 0 (non-arc volcanoes) to ${\Delta }$FMQ 0 to ${+}$2 (arc volcanoes) (where ${\Delta }$FMQ is oxygen fugacity expresses as a log unit difference relative to the Fayalite–Magnetite–Quartz oxygen fugacity buffer). Lower temperature (${

Identifying precursory phenomena is central to the short-range assessment and anticipation of volcanic hazards. The chemistry of gases, which may separate from magma at depth, is operationally monitored at many volcanoes worldwide to manage risk. However, owing to the complexity of volcanic degassing, decoding the message of gas geochemistry has proven challenging. Here, we report an approach to restoration of measured volcanic gas compositions that enables tracking of variations in the temperature and/or oxidation state of the source magma. We validate the approach with reference to independent estimates of melt oxidation state obtained by X-ray absorption near-edge structure (XANES) spectroscopy at the iron K-edge. We then apply the method to a global database of high temperature volcanic gases and to extended gas geochemical timeseries at Unzen, Aso, and Asama volcanoes, identifying hitherto unreported but significant changes in magma intensive parameters that preceded or accompanied changes in volcanic activity. Restoration of volcanic gas compositions offers a promising complement to monitoring strategies at active volcanoes, calling for more systematic operational surveillance of redox-sensitive gas species.

We present a new set of reference materials, the ND70‐series, for in situ measurement 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/m H2O, from 0 to 1.6% m/m CO2 and from 0 to 1% m/m S, 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 CO2 mass 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. [ABSTRACT FROM AUTHOR]

The behavior of Fe3+ during mantle partial melting strongly influences the oxidation state of the resulting magmas, with implications for the evolution of the atmosphere's oxidation state. Here, we challenge a prevailing view that low‐degree partial melts are more oxidized due to the incompatible behavior of Fe3+. Our study is based on measurements of Fe3+/∑Fe along with major, minor, trace and volatile elements in olivine‐ and plagioclase‐hosted melt inclusions of CO2 undersaturated mantle melts in South West Indian Ridge lava. These inclusions record minimum entrapment pressures equivalent to depths up to 10 km below the seafloor, record magma ascent rates of 0.03–0.19 m/s, and display exceptionally high CO2/Ba, CO2/Rb, and CO2/Nb ratios, indicative of a CO2‐rich mantle source. Accounting for fractional crystallization, we find a uniform melt oxidation state (with an Fe3+/ΣFe at 0.140 ± 0.005 at MgO = 10 wt.%) that displays no systematic variation with major, minor, volatile or trace element contents, thus providing no evidence for a relationship between the degree of partial melting and Fe3+/ΣFe. This can be explained by efficient buffering of Fe3+/∑Fe and fO2 of mid‐ocean ridge basalt melts by their surrounding mantle and/or a decrease in the bulk peridotite‐melt Fe2O3 partition coefficient with increasing partial melting. We conclude that changes in the Earth's upper mantle temperature over geological time need not have affected the oxidation state of volcanic products or of the atmosphere. Key Points: Discovery and characterization of a new suite of CO2‐undersaturated melt inclusionsHigh CO2/CITE ratio suggests a CO2‐rich mantle domainNo relation between degree of partial melting and Fe3+/ΣFe indicates efficient buffering or decreasing Fe2O3 partition coefficient with T [ABSTRACT FROM AUTHOR]

Magma decompression rate is one of the most important parameters in controlling eruption dynamics. One way to determine decompression rate is by fitting a volatile elements diffusion profile to a concentration gradient in crystal‐hosted embayments. Previous studies have used a variety of diffusion models, limiting the possibility for inter‐study comparison. Here, we introduce EMBayment‐Estimated Rates (EMBER), a standalone versatile tool that models diffusion of volatile elements along melt embayments. Our model relies on the pdepe function of MATLAB to calculate diffusion profiles of H2O, CO2, and S through the finite difference method. EMBER uses a grid search seeking out the best fits for decompression rates, initial dissolved concentration of each studied volatile and initial exsolved gas content, while setting three constants: temperature along the ascent and pressure at the beginning and end of the ascent. Our model can compute the rate for basaltic, intermediate, and rhyolitic compositions. We applied EMBER to previous studies to evaluate and validate our model. We then reprocessed "homogeneously" the raw data from the literature for a comparison. In other words, the same protocol was used for each diffusion profiles removing the literature‐specific strategies used to constrain unknown parameters. With this comparison, we found a statistically significant positive correlation between maximum magma decompression rates and explosivity of the related eruption. EMBER is expected to help increase the number of volatile diffusion in embayments studies aiming at constraining magma decompression and ascent rates and to facilitate inter‐study comparisons. Key Points: EMBayment‐Estimated Rates (EMBER) is a new, freely available, Graphical User Interface software that models magma ascent rates for basalt to rhyolite with H2O, CO2, and S diffusion profilesEMBER was validated by reproducing previous published literature dataFor mafic eruptions, we found a notable correlation between maximum recalculated decompression rates and eruption magnitude or plume height [ABSTRACT FROM AUTHOR]