1. Elevated Tropospheric Iodine Over the Central Continental United States: Is Iodine a Major Oxidant of Atmospheric Mercury?
- Author
-
Lee, C. F., Elgiar, T., David, L. M., Wilmot, T. Y., Reza, M., Hirshorn, N., McCubbin, I. B., Shah, V., Lin, J. C., Lyman, S. N., Hallar, A. G., Gratz, L. E., and Volkamer, R.
- Subjects
ATMOSPHERIC chemistry ,MERCURY oxidation ,ATMOSPHERIC models ,ATMOSPHERIC mercury ,CHEMICAL models ,AIR masses - 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 (3,220 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. Iodine‐induced mercury oxidation is missing in atmospheric models, understudied, and helps explain model underestimation of oxidized mercury measurements. Plain Language Summary: Halogens such as chlorine, bromine, and iodine are highly reactive gases that participate in atmospheric chemistry, including ozone destruction, particle formation, modification of greenhouse gas lifetime (i.e., methane, dimethylsulfide), and the oxidation of elemental mercury. Iodine mainly enters the atmosphere from oceans; therefore, past measurements of atmospheric iodine have focused on marine and polar regions. This study describes the first lower atmospheric measurements of iodine monoxide (IO) radicals at a remote mountaintop site in the central continental United States. These measurements indicate that the concentration of IO radicals showed a large range over the course of 1 month and reached levels up to three times higher than predicted by a global atmospheric chemistry model. These observations suggest that our understanding of the iodine sources and sinks to the free troposphere may be incomplete. Moreover, we suggest that iodine's contribution to ozone destruction and mercury chemistry may be underestimated; in particular, iodine may be competitive with bromine in the oxidation of elemental mercury in the free troposphere. Key Points: Measurements of iodine monoxide radicals at Storm Peak Laboratory are up to three times higher than predicted by GEOS‐ChemIO tropospheric column variability is significant and highlights a need to better understand sources and sinks of tropospheric iodineIodine may rival bromine as a tropospheric mercury oxidant; iodine‐mercury chemistry is understudied and missing in atmospheric models [ABSTRACT FROM AUTHOR] more...
- Published
- 2024
- Full Text
- View/download PDF