Anthropogenic Influence on Tropospheric Reactive Bromine Since the Pre‐industrial: Implications for Arctic Ice‐Core Bromine Trends

Author:

Zhai Shuting1ORCID,McConnell Joseph R.2ORCID,Chellman Nathan2ORCID,Legrand Michel3ORCID,Opel Thomas4ORCID,Meyer Hanno4ORCID,Jaeglé Lyatt1ORCID,Confer Kaitlyn15ORCID,Fujita Koji6ORCID,Wang Xuan7ORCID,Alexander Becky1ORCID

Affiliation:

1. Department of Atmospheric Sciences University of Washington Seattle WA USA

2. Division of Hydrologic Sciences Desert Research Institute Reno NV USA

3. Université Paris Cité and University Paris Est Creteil CNRS LISA Paris France

4. Alfred Wegener Institute Helmholtz Centre for Polar and Marine Research Potsdam Germany

5. Now at Natural Power Seattle WA USA

6. Graduate School of Environmental Studies Nagoya University Nagoya Japan

7. School of Energy and Environment City University of Hong Kong Kowloon Hong Kong

Abstract

AbstractTropospheric reactive bromine (Bry) influences the oxidation capacity of the atmosphere by acting as a sink for ozone and nitrogen oxides. Aerosol acidity plays a crucial role in Bry abundances through acid‐catalyzed debromination from sea‐salt‐aerosol, the largest global source. Bromine concentrations in a Russian Arctic ice‐core, Akademii Nauk, show a 3.5‐fold increase from pre‐industrial (PI) to the 1970s (peak acidity, PA), and decreased by half to 1999 (present day, PD). Ice‐core acidity mirrors this trend, showing robust correlation with bromine, especially after 1940 (r = 0.9). Model simulations considering anthropogenic emission changes alone show that atmospheric acidity is the main driver of Bry changes, consistent with the observed relationship between acidity and bromine. The influence of atmospheric acidity on Bry should be considered in interpretation of ice‐core bromine trends.

Funder

National Science Foundation

Publisher

American Geophysical Union (AGU)

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