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[1] We report measurements of Hg, SO 2 , and halogens (HCl, HBr, HI) in volcanic gases from Masaya volcano, Nicaragua, and gaseous SO 2 and halogens from Telica volcano, Nicaragua. Mercury measurements were made with a Lumex 915+ portable mercury vapor analyzer and gold traps, while halogens, CO 2 and S species were monitored with a portable multi gas sensor and filter packs. Lumex Hg concentrations in the plume were consistently above background and ranged up to 350 ng m À3. Hg/SO 2 mass ratios measured with the real-time instruments ranged from 1.1 Â 10 À7 to 3.5 Â 10 À5 (mean 2 Â 10 À5

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In volcanoes with active hydrothermal systems, diffuse CO2 degassing may constitute the primary mode of volcanic degassing. The monitoring of CO2 emissions can provide important clues in understanding the evolution of volcanic activity especially at calderas where the interpretation of unrest signals is often complex. Here, we report eighteen years of CO2 fluxes from the soil at Solfatara of Pozzuoli, located in the restless Campi Flegrei caldera. The entire dataset, one of the largest of diffuse CO2 degassing ever produced, is made available for the scientific community. We show that, from 2003 to 2016, the area releasing deep-sourced CO2 tripled its extent. This expansion was accompanied by an increase of the background CO2 flux, over most of the surveyed area (1.4 km2), with increased contributions from non-biogenic source. Concurrently, the amount of diffusively released CO2 increased up to values typical of persistently degassing active volcanoes (up to 3000 t d−1). These variations are consistent with the increase in the flux of magmatic fluids injected into the hydrothermal system, which cause pressure increase and, in turn, condensation within the vapor plume feeding the Solfatara emission.

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We review the state of knowledge on global volcanogenic Hg emissions to the atmosphere and present new data from seven active volcanoes (Poás, Rincón de la Vieja, Turrialba, Aso, Mutnovsky, Gorely and Etna) and two geothermal fields (Las Pailas and Las Hornillas). The variability of Hg contents (c. 4–125 ng m−3) measured in gaseous emissions reflects the dynamic nature of volcanic plumes, where the abundances of volatiles are determined by the physical nature of degassing and variable air dilution. Based on our dataset and previous work, we propose that an average Hg/SO2 plume mass ratio of c. 7.8×10−6 (±1.5×10−6; 1 SE, n=13) is best representative of open-conduit quiescent degassing. Taking into account the uncertainty in global SO2 emissions, we infer a global volcanic Hg flux from persistent degassing of c. 76±30 t a−1. Our data are derived from active volcanoes during non-eruptive periods and we do not have any direct constraint on the Hg flux during periods of elevated SO2 flux associated with large-scale effusive or explosive eruptions. This suggests that the time-averaged Hg flux from these volcanoes is even larger if the eruptive contribution is considered. Conversely, closed-conduit degassing and geothermal emissions contribute modest amounts of Hg