R. S. Martin

High-temperature mixtures of magmatic and atmospheric gases

Recent measurements of BrO, NOx, and near-source sulfate in volcanic plumes suggest that volcanic vents might not simply act as point sources of emissions into the troposphere, but may also act as high-temperature reaction sites where mixtures of magmatic and ambient atmospheric gases may combine, giving new and previously unexpected reaction products. The detection of such species demands that a more complex model be developed for the interaction of volcanoes and atmospheres. We show that general thermodynamic models can be applied successfully to volcanic gas equilibria by comparing the results from HSC Chemistry with those from two volcanic gas equilibrium models (Solvgas and Gasmix). Using a thermodynamic model optimized for volcanic gas chemistry (C-O-S-H-F-Cl-Br-I-N-Ar speciation), we show that the volume ratio of atmospheric gas to magmatic gas in a high-temperature mixture is an important parameter of the volcanic plume chemistry, and our results suggest that even small amounts of air (a few % for an H2O-rich magmatic gas) in the high-temperature mixture are sufficient to yield elevated levels of reactive nitrogen, halogen (Cl, Br, and I), and sulfur species within the volcanic plume. Further modifications of the plume chemistry may also occur due to low-temperature reactions, and chemical schemes for the modification of halogen (Cl, Br, I), nitrogen, and sulfur chemistry are suggested, within the constraints imposed by recent measurements.

Excess volatiles supplied by mingling of mafic magma at an andesite arc volcano

We present the results of a study of volcanic gases at Soufriere Hills Volcano, Montserrat, which includes the first spectroscopic measurements of the major gas species CO2 and H2S at this volcano using a Multisensor Gas Analyzer System (MultiGAS) sensor. The fluxes of CO2 and H2S were 640.2750 t/d and 84.266 t/d, respectively, during July 2008, during a prolonged eruptive pause. The flux of CO2 is similar to estimates for the entire arc from previous geochemical studies, while the measured H2S flux significantly alters our interpretation of the sulphur budget for this volcano. The fluxes of both sulphur and carbon show considerable excesses over that which can be supplied by degassing of erupted magma. We demonstrate, using thermodynamic models and published constraints on preeruptive volatile concentrations, that the gas composition and fluxes are best modeled by mixing between (1) gases derived from isobaric quenching of mafic magma against cooler andesite magma at depth and (2) gases derived from shallower rhyolitic interstitial melt within the porpyritic andesite. The escape of deep-derived gases requires pervasive permeability or vapor advection extending to several kilometers depth in the conduit and magma storage system. These results provide more compelling evidence for both the contribution of unerupted mafic magma to the volatile budget of this andesitic arc volcano and the importance of the intruding mafic magma in sustaining the eruption. From a broader perspective, this study illustrates the importance and role of underplating mafic magmas in arc settings. These magmas play an important role in triggering and sustaining eruptions and contribute in a highly significant way to the volatile budget of arc volcanoes. Copyright

A total volatile inventory for Masaya Volcano, Nicaragua

NERC project “Magma dynamics at persistently degassing basaltic volcanoes: A novel approach to linking volcanic gases and magmatic volatiles within a physical model” (NE/F004222/1 and NE/F005342/1).