Dispersion and Aging of Volcanic Aerosols After the La Soufrière Eruption in April 2021

Author:

Bruckert J.1ORCID,Hirsch L.2,Horváth Á.3ORCID,Kahn R. A.4ORCID,Kölling T.2,Muser L. O.15ORCID,Timmreck C.2ORCID,Vogel H.1ORCID,Wallis S.6ORCID,Hoshyaripour G. A.1ORCID

Affiliation:

1. Institute of Meteorology and Climate Research Karlsruhe Institute of Technology (KIT) Karlsruhe Germany

2. Max‐Planck‐Institut für Meteorologie Hamburg Germany

3. Meteorological Institute Universität Hamburg Hamburg Germany

4. Earth Science Division NASA Goddard Space Flight Center MD Greenbelt USA

5. Now at Alfred Wegener Institute of Polar and Marine Research (AWI) Bremerhaven Germany

6. Institute of Physics University of Greifswald Greifswald Germany

Abstract

AbstractVolcanic aerosols change the atmospheric composition and thereby affect weather and climate. Aerosol dynamic processes such as nucleation, condensation, and coagulation modify the shape, size, and mass of aerosol particles, which influence their atmospheric lifetime and radiative properties. Nevertheless, most models omit these processes for ash particles. In this work, we explore the ash aerosol aging and sulfate production during the first 4 days following the 2021 La Soufrière (St. Vincent) eruption with the ICON‐ART model (ICOsahedral Nonhydrostatic model with Aerosol and Reactive Trace gases). Online coupling of ICON‐ART with a one‐dimensional volcanic plume model calculates volcanic emission, which makes it possible to resolve the different eruption phases of the noncontinuous La Soufrière eruption. We compared our simulated aerosol distribution and composition with observations from the Cloud‐Aerosol Lidar with Orthogonal Polarization (CALIOP) instrument, the Multiangle Imaging SpectroRadiometer (MISR) Research Aerosol (RA) Algorithm, and the Barbados Cloud Observatory (BCO). We show that online coupling is essential to adequately model the emissions and plume development close to the volcano. The modeled aerosol aging is in very good agreement with observations from MISR near the emission source and with CALIOP at larger distances. Furthermore, particle aging occurs faster in the troposphere than in the stratosphere due to the availability of water vapor and OH, but a layer of coated ash appears at the plume top due to faster oxidation of SO2 and lofting by aerosol‐radiation interaction. This paper gives the first direct comparison of aerosol aging in volcanic eruption plumes between simulations and observations.

Funder

Deutsche Forschungsgemeinschaft

Publisher

American Geophysical Union (AGU)

Subject

Space and Planetary Science,Earth and Planetary Sciences (miscellaneous),Atmospheric Science,Geophysics

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