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Effects of Sea Salt Aerosol Emissions for Marine Cloud Brightening on Atmospheric Chemistry: Implications for Radiative Forcing.
Horowitz, Hannah M; Holmes, Christopher; Wright, Alicia; Sherwen, Tomás; Wang, Xuan; Evans, Mat; Huang, Jiayue; Jaeglé, Lyatt; Chen, Qianjie; Zhai, Shuting; Alexander, Becky.
Afiliação
  • Horowitz HM; JISAO University of Washington Seattle WA USA.
  • Holmes C; Department of Atmospheric Sciences University of Washington Seattle WA USA.
  • Wright A; Department of Civil and Environmental Engineering University of Illinois at Urbana-Champaign Urbana IL USA.
  • Sherwen T; Department of Earth, Ocean and Atmospheric Science Florida State University Tallahassee FL USA.
  • Wang X; Department of Atmospheric Sciences University of Washington Seattle WA USA.
  • Evans M; Department of Chemistry University of York York UK.
  • Huang J; Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry University of York York UK.
  • Jaeglé L; School of Energy and Environment City University of Hong Kong Hong Kong.
  • Chen Q; John A. Paulson School of Engineering and Applied Sciences Harvard University Cambridge MA USA.
  • Zhai S; Department of Chemistry University of York York UK.
  • Alexander B; Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry University of York York UK.
Geophys Res Lett ; 47(4): e2019GL085838, 2020 Feb 28.
Article em En | MEDLINE | ID: mdl-32713977
Marine cloud brightening (MCB) is proposed to offset global warming by emitting sea salt aerosols to the tropical marine boundary layer, which increases aerosol and cloud albedo. Sea salt aerosol is the main source of tropospheric reactive chlorine (Cl y ) and bromine (Br y ). The effects of additional sea salt on atmospheric chemistry have not been explored. We simulate sea salt aerosol injections for MCB under two scenarios (212-569 Tg/a) in the GEOS-Chem global chemical transport model, only considering their impacts as a halogen source. Globally, tropospheric Cl y and Br y increase (20-40%), leading to decreased ozone (-3 to -6%). Consequently, OH decreases (-3 to -5%), which increases the methane lifetime (3-6%). Our results suggest that the chemistry of the additional sea salt leads to minor total radiative forcing compared to that of the sea salt aerosol itself (~2%) but may have potential implications for surface ozone pollution in tropical coastal regions.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article