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The influence of ocean halogen and sulfur emissions in the air quality of a coastal megacity: The case of Los Angeles
Muñiz-Unamunzaga, M., R. Borge, G. Sarwar, B. Gantt, D. de la Paz, C. Cuevas, AND A. Saiz-Lopez. The influence of ocean halogen and sulfur emissions in the air quality of a coastal megacity: The case of Los Angeles. SCIENCE OF THE TOTAL ENVIRONMENT. Elsevier BV, AMSTERDAM, Netherlands, 610(611):1536-1545, (2018).
Highlights • Natural marine emissions (Cl, Br, I and DMS) included in CMAQ simulations over LA. • Oceanic halogens and DMS may play an important role on coastal urban areas. • Substantial changes in the levels of key urban atmospheric oxidants (OH, HO2 and NO3). • O3 and NO2 ambient levels decreased by 5 ppbv and 2.5 ppbv in Los Angeles city. • 10% increase in secondary organic aerosol (SOA) due to dimethyl sulphide (DMS).
The oceans are the main source of natural halogen and sulfur compounds, which have a significant influence on the oxidizing capacity of the marine atmosphere; however, their impact on the air quality of coastal cities is currently unknown. We explore the effect of marine halogens (Cl, Br and I) and dimethyl sulfide (DMS) on the air quality of a large coastal city through a set of high-resolution (4-km) air quality simulations for the urban area of Los Angeles, US, using the Community Multiscale Air Quality (CMAQ model). The results indicate that marine halogen emissions decrease ozone and nitrogen dioxide levels up to 5 ppbv and 2.5 ppbv, respectively, in the city of Los Angeles. Previous studies suggested that the inclusion of chlorine in air quality models leads to the generation of ozone in urban areas through photolysis of nitryl chloride (ClNO2). However, we find that when considering the chemistry of Cl, Br and I together the net effect is a reduction of surface ozone concentrations. Furthermore, combined ocean emissions of halogens and DMS cause substantial changes in the levels of key urban atmospheric oxidants such as OH, HO2 and NO3, and in the composition and mass of fine particles. Although the levels of ozone, NO3 and HOx are reduced, we find a 10% increase in secondary organic aerosol (SOA) mean concentration, attributed to the increase in aerosol acidity and sulfate aerosol formation when combining DMS and bromine. Therefore, this new pathway for enhanced SOA formation may potentially help with current model under predictions of urban SOA. Although further observations and research are needed to establish these preliminary conclusions, this first city-scale investigation suggests that the inclusion of oceanic halogens and DMS in air quality models may improve regional air quality predictions over coastal cities around the world.
Record Details:Record Type: DOCUMENT (JOURNAL/PEER REVIEWED JOURNAL)
Organization:U.S. ENVIRONMENTAL PROTECTION AGENCY
OFFICE OF RESEARCH AND DEVELOPMENT
NATIONAL EXPOSURE RESEARCH LABORATORY
COMPUTATIONAL EXPOSURE DIVISION