Influence of bromine and iodine chemistry on annual, seasonal, diurnal, and background ozone: CMAQ simulations over the Northern Hemisphere.

CMAQ background ozone bromine iodine ozone

Journal

Atmospheric environment (Oxford, England : 1994)
ISSN: 1352-2310
Titre abrégé: Atmos Environ (1994)
Pays: England
ID NLM: 9888534

Informations de publication

Date de publication:
2019
Historique:
entrez: 20 7 2019
pubmed: 20 7 2019
medline: 20 7 2019
Statut: ppublish

Résumé

Bromine and iodine chemistry has been updated in the Community Multiscale Air Quality (CMAQ) model to better capture the influence of natural emissions from the oceans on ozone concentrations. Annual simulations were performed using the hemispheric CMAQ model without and with bromine and iodine chemistry. Model results over the Northern Hemisphere show that including bromine and iodine chemistry in CMAQ not only reduces ozone concentrations within the marine boundary layer but also aloft and inland. Bromine and iodine chemistry reduces annual mean surface ozone over seawater by 25%, with lesser ozone reductions over land. The bromine and iodine chemistry decreases ozone concentration without changing the diurnal profile and is active throughout the year. However, it does not have a strong seasonal influence on ozone over the Northern Hemisphere. Model performance of CMAQ is improved by the bromine and iodine chemistry when compared to observations, especially at coastal sites and over seawater. Relative to bromine, iodine chemistry is approximately four times more effective in reducing ozone over seawater over the Northern Hemisphere (on an annual basis). Model results suggest that the chemistry modulates intercontinental transport and lowers the background ozone imported to the United States.

Identifiants

pubmed: 31320831
doi: 10.1016/j.atmosenv.2019.06.020
pmc: PMC6638568
mid: NIHMS1533389
doi:

Types de publication

Journal Article

Langues

eng

Pagination

395-404

Subventions

Organisme : Intramural EPA
ID : EPA999999
Pays : United States

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Auteurs

Golam Sarwar (G)

National Exposure Research Laboratory, US Environmental Protection Agency, RTP, North Carolina 27711, USA.

Brett Gantt (B)

Office of Air Quality Planning and Standards, US Environmental Protection Agency, RTP, NC 27711, USA.

Kristen Foley (K)

National Exposure Research Laboratory, US Environmental Protection Agency, RTP, North Carolina 27711, USA.

Kathleen Fahey (K)

National Exposure Research Laboratory, US Environmental Protection Agency, RTP, North Carolina 27711, USA.

Tanya L Spero (TL)

National Exposure Research Laboratory, US Environmental Protection Agency, RTP, North Carolina 27711, USA.

Daiwen Kang (D)

National Exposure Research Laboratory, US Environmental Protection Agency, RTP, North Carolina 27711, USA.

Rohit Mathur (R)

National Exposure Research Laboratory, US Environmental Protection Agency, RTP, North Carolina 27711, USA.

Hosein Foroutan (H)

The Charles E. Via, Jr. Department of Civil & Environmental Engineering, Virginia Tech, Blacksburg 24061, USA.

Jia Xing (J)

State Key Joint Laboratory of Environmental Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 100084, China.

Tomás Sherwen (T)

Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry, University of York, UK.
National Centre for Atmospheric Science, Department of Chemistry, University of York, UK.

Alfonso Saiz-Lopez (A)

Department of Atmospheric Chemistry and Climate, Institute of Physical Chemistry Rocasolano, CSIC, Madrid 28006, Spain.

Classifications MeSH