Fogs and Air Quality on the Southern California Coast

Received: November 30, 2016
Revised: March 16, 2017
Accepted: March 19, 2017
Download Citation: RIS|BibTeX|https://doi.org/10.4209/aaqr.2016.11.0522  

Cite this article:

Boris, A.J., Napolitano, D.C., Herckes, P., Clements, A.L. and Collett, Jr., J.L. (2018). Fogs and Air Quality on the Southern California Coast. Aerosol Air Qual. Res. 18: 224-239. https://doi.org/10.4209/aaqr.2016.11.0522

HIGHLIGHTS

• Aqueous formation of carboxylic acids, organic nitrogen and sulfur species suggested.
• Oil and natural gas processing, mobile sources predominant emissions sources.
• Successful regulations likely explain improvements in air quality since 1985/6.

ABSTRACT

Fog acts as a reservoir and transport vector for chemicals in the atmosphere, altering the distribution of species between the gas and particle phases, and allowing deposition of nutrients and pollutants onto ecosystems and crops. Fog water and trace gas samples were collected from Casitas Pass along the Santa Barbara Channel in June 2015 to identify emissions sources and aqueous processes impacting Southern California air. Fog water composition was dominated by NH₄⁺ (volume weighted mean, VWM = 232 µM, range = 85–640 µM), with lesser contributions from NO₃^– (126 µM, 30.4–778 µM) and SO₄^2– (28.3 µM, 12.1–90.0 µM), pushing the VWM pH to 5.92 (5.34–6.67). Organic carbon contributed substantially to fog composition (8.27 mg C L^–1, 4.70–16.8 mg C L^–1). Carboxylic acids, products of aqueous oxidation, were abundant (20.1% of carbon mass on average), with > 1% contributions by acetate, formate, oxalate, malonate, succinate, and lactate. Sulfur- and nitrogen-containing organic species were detected, often after 3–5 hours of fog, suggesting aqueous formation. Sampled air was advected over the coastline near oil extraction operations, urban and agricultural areas; regional oil and natural gas processing and mobile sources were the most influential organic emissions at Casitas Pass. Fog composition in 2015 was contrasted with that from a study in July-September 1985/6. Concentrations of major fog constituents appear to have decreased in response to successful air quality regulations. While natural species concentrations in fog were similar (e.g., 2015 VWM [Na⁺] = 101 µM, range = < 30–320 µM; 1985/6 [Na⁺] = 129 µM, 12–1000 µM), anthropogenic species concentrations were lower in 2015 (e.g., 1985/6: [NO₃^–] = 236 µM, 141–2800 µM vs. 2015: 126 µM, 30.4–778 µM). These results overall highlight changes in Southern California air quality issues, including improvement of some anthropogenic emissions and the current influence of organic emissions from industrial and mobile sources.

Keywords: Fog chemistry; Aqueous atmospheric chemistry; Aqueous secondary organic aerosol; Organic sulfur; Organic nitrogen.