Surface volcanic gases may reflect volatile budgets of magma and forecast impending eruptions, and their release to the atmosphere may affect climate. The dynamics of magma degassing is complicated, however, by differences in the solubility, partitioning, and diffusion of the various volatiles, all of which can vary with pressure, temperature, and melt composition. To constrain possible gas outputs, we carried out experiments to determine how Cl partitions between water bubbles and silicate melt, and decompression experiments to examine how Cl behaves duringclosed-and open-system degassing. We incorporate our findings and those from the literature for CO 2 and S into a steady, isothermal, and homogeneous flow model to estimate fluxes of gases at the vent from ascending water-rich magma, assuming different scenarios for the onset and development of permeability in bubbly magma. We find that, for given permeability scenarios, total gas fluxes vary with magma flux, but ratios of gas species do not change. The S/Cl and SO 2 /CO 2 ratios do change, however, depending on whether the magma is oxidized or reduced. After magma fragments into a Plinian eruption column gases continue to escape from cooling pumice in the plume, but here the rate of gas release is controlled by diffusion, which varies with temperature.Degassing of pumice and ash was modeled by linking a steady-state plume model, which gives the vertical variation of mean temperature and velocity of particles inside the plume, to a conductive cooling model of pumices, which controls diffusion of Cl, CO 2 , and S in pumice. We find that gas loss increases with column height (mass flux) and initial temperature, because in both cases pumices cool over a longer time period, allowing more gas to diffuse out of the matrix glass. The amount of gas released also depends on the size distribution of particles in the erupting mixture, with less being released for a finely skewed distribution.