Observational-based assessment of contributions to maximum ozone concentrations in the western United States.

Archived Ozone Design Values (ODVs) provide smoothed temporal records of maximum ozone concentrations impacting monitoring sites throughout the US. Utilizing time series of ODVs recorded at sites along the US West Coast, we separately estimate ODV contributions from US background ozone and from production driven by US anthropogenic precursor emissions. Sondes launched from Trinidad Head in northern California measure the vertical distribution of baseline ozone transported ashore from the Pacific; this profile is reflected in the increase of the US background ODV contribution with monitoring site elevation in both rural and urban areas.

Large contribution of biomass burning emissions to ozone throughout the global remote troposphere.

Ozone is the third most important anthropogenic greenhouse gas after carbon dioxide and methane but has a larger uncertainty in its radiative forcing, in part because of uncertainty in the source characteristics of ozone precursors, nitrogen oxides, and volatile organic carbon that directly affect ozone formation chemistry. Tropospheric ozone also negatively affects human and ecosystem health. Biomass burning (BB) and urban emissions are significant but uncertain sources of ozone precursors.

Long-term baseline ozone changes in the Western US: A synthesis of analyses.

Quantification of the magnitude and long-term changes in ozone concentrations transported into the U.S. is important for effective air quality policy development.

Quantifying the role of PM dropping in variations of ground-level ozone: Inter-comparison between Beijing and Los Angeles.

In recent decade the ambient fine particle (PM) levels have shown a trend of distinct dropping in China, while ground-level ozone concentrations have been increasing in Beijing and many other Chinese mega-cities. The variation pattern in Los Angeles was markedly different, with PM and ozone decreasing together over past decades. In this study, we utilize observation-based methods to establish the parametric relationship between PM concentration and key aerosol physical properties (including aerosol optical depth and aerosol surface concentration), and an observation-based 1-D photochemical model to quantify the response of PM decline in enhancing ground-level ozone pollution over a large PM concentration range (10-120 μg m).

High winter ozone pollution from carbonyl photolysis in an oil and gas basin.

The United States is now experiencing the most rapid expansion in oil and gas production in four decades, owing in large part to implementation of new extraction technologies such as horizontal drilling combined with hydraulic fracturing. The environmental impacts of this development, from its effect on water quality to the influence of increased methane leakage on climate, have been a matter of intense debate. Air quality impacts are associated with emissions of nitrogen oxides (NOx = NO + NO2) and volatile organic compounds (VOCs), whose photochemistry leads to production of ozone, a secondary pollutant with negative health effects.

Magnitude, decadal changes, and impact of regional background ozone transported into the greater Houston, Texas, area.

Two independent analyses of the daily maximum 8 h average ozone concentrations measured during the high ozone season (May through October) at Continuous Ambient Monitoring Stations are used to quantify the regional background ozone transported into the Houston-Galveston-Brazoria (HGB) area. The dependence on wind direction is examined, and long-term trends are determined using measurements made between 1998 and 2012. Both analyses show that the regional background ozone has declined during periods of continental outflow: i.

Chemical data quantify Deepwater Horizon hydrocarbon flow rate and environmental distribution.

Detailed airborne, surface, and subsurface chemical measurements, primarily obtained in May and June 2010, are used to quantify initial hydrocarbon compositions along different transport pathways (i.e., in deep subsurface plumes, in the initial surface slick, and in the atmosphere) during the Deepwater Horizon oil spill.

Air quality implications of the Deepwater Horizon oil spill.

During the Deepwater Horizon (DWH) oil spill, a wide range of gas and aerosol species were measured from an aircraft around, downwind, and away from the DWH site. Additional hydrocarbon measurements were made from ships in the vicinity. Aerosol particles of respirable sizes were on occasions a significant air quality issue for populated areas along the Gulf Coast.

Establishing policy relevant background (PRB) ozone concentrations in the United States.

Policy Relevant Background (PRB) ozone concentrations are defined by the United States (U.S.) Environmental Protection Agency (EPA) as those concentrations that would occur in the U.

Temporal changes in U.S. benzene emissions inferred from atmospheric measurements.

The 1990 Clean Air Act Amendments required the United States Environmental Protection Agency (U.S. EPA) to enact stricter regulations aimed at reducing benzene emissions.