Summertime Primary and Secondary Contributions to Southern Ocean Cloud Condensation Nuclei

International audience Atmospheric aerosols in clean remote oceanic regions contribute significantly to the global albedo through the formation of haze and cloud layers; however, the relative importance of ‘primary’ wind-produced sea-spray over secondary (gas-to-particle conversion) sulphate in form...

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Bibliographic Details
Published in:Scientific Reports
Main Authors: Fossum, Kirsten N., Ovadnevaite, Jurgita, Ceburnis, Darius, Dall’osto, Manuel, Marullo, Salvatore, Bellacicco, Marco, Simo, Rafel, Liu, Dantong, Flynn, Michael, Zuend, Andreas, O’dowd, Colin
Other Authors: Laboratoire d'océanographie de Villefranche (LOV), Institut national des sciences de l'Univers (INSU - CNRS)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de la Mer de Villefranche (IMEV), Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Format: Article in Journal/Newspaper
Language:English
Published: HAL CCSD 2018
Subjects:
Online Access:https://hal.sorbonne-universite.fr/hal-01885116
https://hal.sorbonne-universite.fr/hal-01885116/document
https://hal.sorbonne-universite.fr/hal-01885116/file/s41598-018-32047-4.pdf
https://doi.org/10.1038/s41598-018-32047-4
Description
Summary:International audience Atmospheric aerosols in clean remote oceanic regions contribute significantly to the global albedo through the formation of haze and cloud layers; however, the relative importance of ‘primary’ wind-produced sea-spray over secondary (gas-to-particle conversion) sulphate in forming marine clouds remains unclear. Here we report on marine aerosols (PM1) over the Southern Ocean around Antarctica, in terms of their physical, chemical, and cloud droplet activation properties. Two predominant pristine air masses and aerosol populations were encountered: modified continental Antarctic (cAA) comprising predominantly sulphate with minimal sea-salt contribution and maritime Polar (mP) comprising sulphate plus sea-salt. We estimate that in cAA air, 75% of the CCN are activated into cloud droplets while in mP air, 37% are activated into droplets, for corresponding peak supersaturation ranges of 0.37–0.45% and 0.19–0.31%, respectively. When realistic marine boundary layer cloud supersaturations are considered (e.g. ~0.2–0.3%), sea-salt CCN contributed 2–13% of the activated nuclei in the cAA air and 8–51% for the marine air for surface-level wind speed < 16 m s−1. At higher wind speeds, primary marine aerosol can even contribute up to 100% of the activated CCN, for corresponding peak supersaturations as high as 0.32%.