Massive volcanic SO(2) oxidation and sulphate aerosol deposition in Cenozoic North America.

Volcanic eruptions release a large amount of sulphur dioxide (SO(2)) into the atmosphere. SO(2) is oxidized to sulphate and can subsequently form sulphate aerosol, which can affect the Earth's radiation balance, biologic productivity and high-altitude ozone concentrations, as is evident from recent volcanic eruptions. SO(2) oxidation can occur via several different pathways that depend on its flux and the atmospheric conditions. An investigation into how SO(2) is oxidized to sulphate-the oxidation product preserved in the rock record-can therefore shed light on past volcanic eruptions and atmospheric conditions. Here we use sulphur and triple oxygen isotope measurements of atmospheric sulphate extracted from tuffaceous deposits to investigate the specific oxidation pathways from which the sulphate was formed. We find that seven eruption-related sulphate aerosol deposition events have occurred during the mid-Cenozoic era (34 to 7 million years ago) in the northern High Plains, North America. Two extensively sampled ash beds display a similar sulphate mixing pattern that has two distinct atmospheric secondary sulphates. A three-dimensional atmospheric sulphur chemistry and transport model study reveals that the observed, isotopically discrete sulphates in sediments can be produced only in initially alkaline cloudwater that favours an ozone-dominated SO(2) oxidation pathway in the troposphere. Our finding suggests that, in contrast to the weakly acidic conditions today, cloudwater in the northern High Plains may frequently have been alkaline during the mid-Cenozoic era. We propose that atmospheric secondary sulphate preserved in continental deposits represents an unexploited geological archive for atmospheric SO(2) oxidation chemistry linked to volcanism and atmospheric conditions in the past.