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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]