Observations of I2 at a remote marine site

Inorganic iodine plays a significant role in the photochemistry of the marine boundary layer, but the sources and cycling of iodine are not well understood. We report the first I2 observations in marine air that is not impacted by coastal macroalgal emissions or sea ice chemistry. The data clearly d...

Full description

Bibliographic Details
Published in:Atmospheric Chemistry and Physics
Main Authors: Lawler, M.J., Mahajan, Anoop S., Saiz-Lopez, A., Saltzman, E.S.
Format: Article in Journal/Newspaper
Language:unknown
Published: European Geophysical Society 2014
Subjects:
Online Access:http://hdl.handle.net/10261/167796
https://doi.org/10.5194/acp-14-2669-2014
id ftcsic:oai:digital.csic.es:10261/167796
record_format openpolar
spelling ftcsic:oai:digital.csic.es:10261/167796 2024-02-11T10:08:33+01:00 Observations of I2 at a remote marine site Lawler, M.J. Mahajan, Anoop S. Saiz-Lopez, A. Saltzman, E.S. 2014 http://hdl.handle.net/10261/167796 https://doi.org/10.5194/acp-14-2669-2014 unknown European Geophysical Society Publisher's version Sí doi:10.5194/acp-14-2669-2014 issn: 1680-7324 Atmospheric Chemistry and Physics 14: 2669- 2678 (2014) http://hdl.handle.net/10261/167796 open artículo http://purl.org/coar/resource_type/c_6501 2014 ftcsic https://doi.org/10.5194/acp-14-2669-2014 2024-01-16T10:31:52Z Inorganic iodine plays a significant role in the photochemistry of the marine boundary layer, but the sources and cycling of iodine are not well understood. We report the first I2 observations in marine air that is not impacted by coastal macroalgal emissions or sea ice chemistry. The data clearly demonstrate that the very high I2 levels previously reported for coastal air are not representative of open ocean conditions. In this study, gas phase I2 was measured at the Cape Verde Atmospheric Observatory, a semi-remote site in the eastern tropical Atlantic, using atmospheric pressure chemical ionization tandem mass spectrometry. Atmospheric I2 levels typically increased beginning at sunset, leveled off after midnight, and then rapidly decreased at sunrise. There was also a smaller midday maximum in I 2 that was probably caused by a measurement artifact. Ambient I 2 mixing ratios ranged from <0.02-0.6 pmol mol-1 in May 2007 and <0.03-1.67 pmol mol-1 in May 2009. The sea-air flux implied by the nighttime buildup of I2 is too small to explain the observed daytime IO levels at this site. Iodocarbon measurements made in this region previously are also insufficient to explain the observed 1-2 pmol mol-1 of daytime IO. The observations imply the existence of an unknown daytime source of gas phase inorganic iodine. Carpenter et al. (2013) recently proposed that sea surface emissions of HOI are several times larger than the flux of I2. Such a flux could account for both the nighttime I2 and the daytime IO observations. © 2014 Author(s). Peer Reviewed Article in Journal/Newspaper Sea ice Digital.CSIC (Spanish National Research Council) Atmospheric Chemistry and Physics 14 5 2669 2678
institution Open Polar
collection Digital.CSIC (Spanish National Research Council)
op_collection_id ftcsic
language unknown
description Inorganic iodine plays a significant role in the photochemistry of the marine boundary layer, but the sources and cycling of iodine are not well understood. We report the first I2 observations in marine air that is not impacted by coastal macroalgal emissions or sea ice chemistry. The data clearly demonstrate that the very high I2 levels previously reported for coastal air are not representative of open ocean conditions. In this study, gas phase I2 was measured at the Cape Verde Atmospheric Observatory, a semi-remote site in the eastern tropical Atlantic, using atmospheric pressure chemical ionization tandem mass spectrometry. Atmospheric I2 levels typically increased beginning at sunset, leveled off after midnight, and then rapidly decreased at sunrise. There was also a smaller midday maximum in I 2 that was probably caused by a measurement artifact. Ambient I 2 mixing ratios ranged from <0.02-0.6 pmol mol-1 in May 2007 and <0.03-1.67 pmol mol-1 in May 2009. The sea-air flux implied by the nighttime buildup of I2 is too small to explain the observed daytime IO levels at this site. Iodocarbon measurements made in this region previously are also insufficient to explain the observed 1-2 pmol mol-1 of daytime IO. The observations imply the existence of an unknown daytime source of gas phase inorganic iodine. Carpenter et al. (2013) recently proposed that sea surface emissions of HOI are several times larger than the flux of I2. Such a flux could account for both the nighttime I2 and the daytime IO observations. © 2014 Author(s). Peer Reviewed
format Article in Journal/Newspaper
author Lawler, M.J.
Mahajan, Anoop S.
Saiz-Lopez, A.
Saltzman, E.S.
spellingShingle Lawler, M.J.
Mahajan, Anoop S.
Saiz-Lopez, A.
Saltzman, E.S.
Observations of I2 at a remote marine site
author_facet Lawler, M.J.
Mahajan, Anoop S.
Saiz-Lopez, A.
Saltzman, E.S.
author_sort Lawler, M.J.
title Observations of I2 at a remote marine site
title_short Observations of I2 at a remote marine site
title_full Observations of I2 at a remote marine site
title_fullStr Observations of I2 at a remote marine site
title_full_unstemmed Observations of I2 at a remote marine site
title_sort observations of i2 at a remote marine site
publisher European Geophysical Society
publishDate 2014
url http://hdl.handle.net/10261/167796
https://doi.org/10.5194/acp-14-2669-2014
genre Sea ice
genre_facet Sea ice
op_relation Publisher's version

doi:10.5194/acp-14-2669-2014
issn: 1680-7324
Atmospheric Chemistry and Physics 14: 2669- 2678 (2014)
http://hdl.handle.net/10261/167796
op_rights open
op_doi https://doi.org/10.5194/acp-14-2669-2014
container_title Atmospheric Chemistry and Physics
container_volume 14
container_issue 5
container_start_page 2669
op_container_end_page 2678
_version_ 1790607924879425536