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Elevated Tropospheric Iodine over the Central Continental United States: Is Iodine a Major Oxidant of Atmospheric Mercury?
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  • Christopher Francis Lee,
  • Tyler Eligar,
  • Liji M David,
  • Taylor Yukai Wilmot,
  • Mago Reza,
  • Noah Hirshorn,
  • Ian B. McCubbin,
  • Viral Shah,
  • John C. Lin,
  • Seth Lyman,
  • A. Gannet Hallar,
  • Lynne E. Gratz,
  • Rainer Volkamer
Christopher Francis Lee
University of Colorado Boulder
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Tyler Eligar
Utah State University
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Liji M David
Ramboll
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Taylor Yukai Wilmot
University of Utah
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Mago Reza
University of Colorado Boulder
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Noah Hirshorn
University of Utah
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Ian B. McCubbin
University of Utah
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Viral Shah
NASA Global Modeling and Assimilation Office and SSAI
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John C. Lin
University of Utah
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Seth Lyman
usu
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A. Gannet Hallar
University of Utah
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Lynne E. Gratz
Reed College
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Rainer Volkamer
University of Colorado Boulder

Corresponding Author:[email protected]

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Abstract

Previous efforts to measure atmospheric iodine have focused on marine and coastal regions. We report the first ground-based tropospheric iodine monoxide (IO) radical observations over the central continental United States. Throughout April 2022, IO columns above Storm Peak Laboratory, Colorado (3220 m.a.s.l.) ranged from 0.7±0.5 to 3.6±0.5×1012 (average: 1.9×1012 molec cm-2). IO was consistently elevated in air masses transported from over the Pacific Ocean. The observed IO columns were up to three times higher and the range was larger than predicted by a global model, which warrants further investigation into iodine sources, sinks, ozone loss, and particle formation. IO mixing ratios increased with altitude. At the observed levels, iodine may be competitive with bromine as an oxidant of elemental mercury at cold temperatures typical of the free troposphere (4–12km; <260K). Iodine-induced mercury oxidation is missing in atmospheric models, understudied, and helps explain model underestimation of oxidized mercury measurements.
19 Mar 2024Submitted to ESS Open Archive
25 Mar 2024Published in ESS Open Archive