Sensitivity of stratospheric ozone to the latitude, season, and halogen content of a contemporary explosive volcanic eruption.

We present a systematic evaluation of the perturbation to the stratosphere from an explosive volcanic eruption injecting sulfur dioxide into the atmosphere, as a function of latitude, season, and injection gas halogen content in a chemistry-climate state representative of the present day (modeled as year 2025). Enhancements in aerosol surface area density and decreases in stratospheric ozone are observed for a period of years following all modeled scenarios, with volcanic eruptions near the equator impacting both hemispheres relatively equally, and eruptions at higher latitudes reducing the thickness of the ozone layer more substantially in the hemisphere of the eruption. Our simulations reveal that there that are significant seasonal differences when comparing the stratospheric impact of a volcanic eruption occurring in summer versus winter, and this holds true regardless of whether volcanic halogen gases (Cl, Br) are co-injected with sulfur dioxide. If an explosive halogen-rich eruption were to occur, there would be substantial ozone losses in both hemispheres, regardless of latitude or season, with recovery potentially exceeding 4 years.

An Improved Electron Microprobe Method for the Analysis of Halogens in Natural Silicate Glasses.

We present a new analytical method, which allows the simultaneous analysis of fluorine (F), chlorine (Cl), bromine (Br), and iodine (I) in geological samples. To account for interferences of Fe on the spectral lines of F, of Al on Br-lines, and of Ca on I-lines, we prepared four new halogen-free calibration glasses. The new method is used to analyze various glass reference materials and crystal-hosted melt inclusions from the Azores. Our results show that our new method allows reliable and reproducible analyses of all four halogens in silicate glasses.

Stratospheric Ozone destruction by the Bronze-Age Minoan eruption (Santorini Volcano, Greece).

The role of volcanogenic halogen-bearing (i.e. chlorine and bromine) compounds in stratospheric ozone chemistry and climate forcing is poorly constrained. While the 1991 eruption of Pinatubo resulted in stratospheric ozone loss, it was due to heterogeneous chemistry on volcanic sulfate aerosols involving chlorine of anthropogenic rather than volcanogenic origin, since co-erupted chlorine was scavenged within the plume. Therefore, it is not known what effect volcanism had on ozone in pre-industrial times, nor what will be its role on future atmospheres with reduced anthropogenic halogens present. By combining petrologic constraints on eruption volatile yields with a global atmospheric chemistry-transport model, we show here that the Bronze-Age 'Minoan' eruption of Santorini Volcano released far more halogens than sulfur and that, even if only 2% of these halogens reached the stratosphere, it would have resulted in strong global ozone depletion. The model predicts reductions in ozone columns of 20 to >90% at Northern high latitudes and an ozone recovery taking up to a decade. Our findings emphasise the significance of volcanic halogens for stratosphere chemistry and suggest that modelling of past and future volcanic impacts on Earth's ozone, climate and ecosystems should systematically consider volcanic halogen emissions in addition to sulfur emissions.