Pollution-enhanced reactive chlorine chemistry in the eastern tropical Atlantic boundary layer

M. J. Lawler, B. D. Finley, W. C. Keene, A. A. P. Pszenny, K. A. Read, R. von Glasow, E. S. Saltzman

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Abstract

[1] This study examines atmospheric reactive chlorine chemistry at the Cape Verde Atmospheric Observatory in the eastern tropical Atlantic. During May-June, 2007, Cl2levels ranged from below detection (~2 ppt) to 30 ppt. Elevated Cl2 was associated with high HNO3 (40 to 120 ppt) in polluted continental outflow transported in the marine boundary layer (MBL) to the site. Lower Cl2 was observed in recently subsided air masses with multiday free tropospheric oceanic trajectories and in air containing Saharan dust. Model simulations show that the observations of elevated Cl2 in polluted marine air are consistent with initiation of Cl chemistry by OH + HC1 and subsequent heterogeneous, autocatalytic Cl cycling involving marine aerosols. Model estimates suggest that Cl atom reactions significantly impact the fates of methane and dimethylsulfide at Cape Verde and are moderately important for ozone cycling.
Original languageEnglish
JournalGeophysical Research Letters
Volume36
Issue number8
DOIs
Publication statusPublished - 2009

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 14 - Life Below Water
    SDG 14 Life Below Water

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