Atmospheric isoprene measurements reveal larger-than-expected Southern Ocean emissions

Author:

Ferracci Valerio1ORCID,Weber James2ORCID,Bolas Conor3,Robinson Andrew3,Tummon Fiona4,Rodríguez-Ros Pablo5ORCID,Cortés Pau5,Baccarini Andrea6ORCID,Jones Rod7,Galí Martí8ORCID,Simó Rafel9ORCID,Schmale Julia10ORCID,Harris Neil1

Affiliation:

1. Cranfield University

2. University of Sheffield

3. University of Cambridge

4. Swiss Federal Office for Meteorology and Climatology MeteoSwiss

5. Institut de Ciències del Mar

6. EPFL

7. Department of Chemistry

8. Institut de Ciències del Mar (ICM-CSIC)

9. Institut de Ciències del Mar, ICM-CSIC

10. École Polytechnique Fédérale de Lausanne

Abstract

Abstract Isoprene is a key trace component of the atmosphere emitted by vegetation and other organisms. It is highly reactive and can impact atmospheric composition and climate by affecting the greenhouse gases ozone and methane and secondary organic aerosol formation. Marine emissions are poorly constrained due to the paucity of long-term measurements: this in turn limits our understanding of isoprene cycling in the ocean. Here we present the analysis of isoprene concentrations in the atmosphere measured across the Southern Ocean over 4 months in the summertime. The highest concentrations originated from the marginal ice zone (MIZ) in the Ross and Amundsen seas, indicating the MIZ is a significant source of isoprene at high latitudes. Using the global chemistry-climate model UKESM1 we show that current estimates of sea-to-air isoprene fluxes underestimate observed isoprene by a factor > 20. A daytime source of isoprene is required to reconcile models with observations. Increased isoprene emissions would lead to > 8% decrease in the hydroxyl radical in regions of the Southern Ocean, with implications for our understanding of atmospheric oxidation and composition in remote environments, often used as proxies for the pre-industrial atmosphere.

Publisher

Research Square Platform LLC

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