Traffic, transport, and vegetation drive VOC concentrations in a major urban area in Texas.

The population of Texas has increased rapidly in the past decade. The San Antonio Field Study (SAFS) was designed to investigate ozone (O3) production and precursors in this rapidly changing, sprawling metropolitan area. There are still many questions regarding the sources and chemistry of volatile organic compounds (VOCs) in urban areas like San Antonio which are affected by a complex mixture of industry, traffic, biogenic sources and transported pollutants. The goal of the SAFS campaign in May 2017 was to measure inorganic trace gases, VOCs, methane (CH4), and ethane (C2H6). The SAFS field design included two sites to better assess air quality across the metro area: an urban site (Traveler's World; TW) and a downwind/suburban site (University of Texas at San Antonio; UTSA). The results indicated that acetone (2.52 ± 1.17 and 2.39 ± 1.27 ppbv), acetaldehyde (1.45 ± 1.02 and 0.93 ± 0.45 ppbv) and isoprene (0.64 ± 0.49 and 1.21 ± 0.85 ppbv; TW and UTSA, respectively) were the VOCs with the highest concentrations. Additionally, positive matrix factorization showed three dominant factors of VOC emissions: biogenic, aged urban mixed source, and acetone. Methyl vinyl ketone and methacrolein (MVK + MACR) exhibited contributions from both secondary photooxidation of isoprene and direct emissions from traffic. The C2H6:CH4 demonstrated potential influence of oil and gas activities in San Antonio. Moreover, the high O3 days during the campaign were in the NOx-limited O3 formation regime and were preceded by evening peaks in select VOCs, NOx and CO. Overall, quantification of the concentration and trends of VOCs and trace gases in a major city in Texas offers vital information for general air quality management and supports strategies for reducing O3 pollution. The SAFS campaign VOC results will also add to the growing body of literature on urban sources and concentrations of VOCs in major urban areas.

The characterization of fine particulate matter downwind of Houston: Using integrated factor analysis to identify anthropogenic and natural sources.

The interpretation of large air pollution datasets involves a great deal of complexity. To gain a better understanding of the complicated relationships and patterns within datasets, we perform factor analysis. Between December 2015 and December 2017, fine particulate matter (PM2.5) samples were collected at a suburban site northeast of the Houston metropolitan area, TX. A total of 233 filter samples were analyzed for chemical composition. The average of all PM2.5 samples consisted of 38.1% inorganic ions, 28.9% elements, 29.1% organic carbon, and 3.7% elemental carbon and other organic materials. Principal component analysis and positive matrix factorization were utilized to identify eight factors: regional aerosols, biomass burning, gasoline combustion, industry, crustal material, incineration, marine dust, and fireworks. The first three contributed more than 70% of the total PM2.5 mass. The receptor models also captured the impact of fireworks and classified it as a source of PM2.5 over Houston. To identify the origins of air masses transporting PM2.5 to the site, we applied the NOAA hybrid single-particle Lagrangian integrated trajectory model and performed a cluster analysis of back trajectories and determined six cluster source regions: the Gulf of Mexico, the Southeast, two midwestern clusters, the Pacific Northwest, and the Southwest. The results of our analysis show that during the summer months, marine and crustal sources were often associated with an onshore flow from the Gulf of Mexico and that four clusters covering 38% of the West Liberty area were strongly influenced by trajectories originating from biomass burning. The results of this study represented a variety of sources that affect the PM2.5 over the Houston metropolitan area. The quantified contributions of these sources could provide policymakers with useful information for developing more efficient control systems and making more effective decisions to cope with the harmful effects of ambient air pollution.

Observing Severe Drought Influences on Ozone Air Pollution in California.

Drought conditions affect ozone air quality, potentially altering multiple terms in the O3 mass balance equation. Here, we present a multiyear observational analysis using data collected before, during, and after the record-breaking California drought (2011-2015) at the O3-polluted locations of Fresno and Bakersfield near the Sierra Nevada foothills. We separately assess drought influences on O3 chemical production ( PO3) from O3 concentration. We show that isoprene concentrations, which are a source of O3-forming organic reactivity, were relatively insensitive to early drought conditions but decreased by more than 50% during the most severe drought years (2014-2015), with recovery a function of location. We find drought-isoprene effects are temperature-dependent, even after accounting for changes in leaf area, consistent with laboratory studies but not previously observed at landscape scales with atmospheric observations. Drought-driven decreases in organic reactivity are contemporaneous with a change in dominant oxidation mechanism, with PO3 becoming more NO x-suppressed, leading to a decrease in PO3 of ∼20%. We infer reductions in atmospheric O3 loss of ∼15% during the most severe drought period, consistent with past observations of decreases in O3 uptake by plants. We consider drought-related trends in O3 variability on synoptic time scales by analyzing statistics of multiday high-O3 events. We discuss implications for regulating O3 air pollution in California and other locations under more prevalent drought conditions.