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Interfacial photochemistry at the ocean surface is a global source of organic vapors and aerosols

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  • Martin Brüggemann

    (Univ Lyon, Université Claude Bernard Lyon 1, CNRS, IRCELYON
    Leibniz Institute for Tropospheric Research (TROPOS))

  • Nathalie Hayeck

    (Univ Lyon, Université Claude Bernard Lyon 1, CNRS, IRCELYON)

  • Christian George

    (Univ Lyon, Université Claude Bernard Lyon 1, CNRS, IRCELYON)

Abstract

The surface of the oceans acts as a global sink and source for trace gases and aerosol particles. Recent studies suggest that photochemical reactions at this air/water interface produce organic vapors, enhancing particle formation in the atmosphere. However, current model calculations neglect this abiotic source of reactive compounds and account only for biological emissions. Here we show that interfacial photochemistry serves as a major abiotic source of volatile organic compounds (VOCs) on a global scale, capable to compete with emissions from marine biology. Our results indicate global emissions of 23.2–91.9 TgC yr–1 of organic vapors from the oceans into the marine atmosphere and a potential contribution to organic aerosol mass of more than 60% over the remote ocean. Moreover, we provide global distributions of VOC formation potentials, which can be used as simple tools for field studies to estimate photochemical VOC emissions depending on location and season.

Suggested Citation

  • Martin Brüggemann & Nathalie Hayeck & Christian George, 2018. "Interfacial photochemistry at the ocean surface is a global source of organic vapors and aerosols," Nature Communications, Nature, vol. 9(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04528-7
    DOI: 10.1038/s41467-018-04528-7
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    Cited by:

    1. Valerio Ferracci & James Weber & Conor G. Bolas & Andrew D. Robinson & Fiona Tummon & Pablo Rodríguez-Ros & Pau Cortés-Greus & Andrea Baccarini & Roderic L. Jones & Martí Galí & Rafel Simó & Julia Sch, 2024. "Atmospheric isoprene measurements reveal larger-than-expected Southern Ocean emissions," Nature Communications, Nature, vol. 15(1), pages 1-11, December.

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