Persisting volcanic ash particles impact stratospheric SO<sub>2</sub> lifetime and aerosol optical properties.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32913208.
- Also identified by DOI 10.1038/s41467-020-18352-5 and PMC identifier 7483524.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Volcanic ash is often neglected in climate simulations because ash particles are assumed to have a short atmospheric lifetime, and to not participate in sulfur chemistry. After the Mt. Kelut eruption in 2014, stratospheric ash-rich aerosols were observed for months. Here we show that the persistence of super-micron ash is consistent with a density near 0.5 g cm<sup>-3</sup>, close to pumice. Ash-rich particles dominate the volcanic cloud optical properties for the first 60 days. We also find that the initial SO<sub>2</sub> lifetime is determined by SO<sub>2</sub> uptake on ash, rather than by reaction with OH as commonly assumed. About 43% more volcanic sulfur is removed from the stratosphere in 2 months with the SO<sub>2</sub> heterogeneous chemistry on ash particles than without. This research suggests the need for re-evaluation of factors controlling SO<sub>2</sub> lifetime in climate model simulations, and of the impact of volcanic ash on stratospheric chemistry and radiation.