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Ozone is one of the six "criteria" pollutants identified by the U.S. Clean Air Act Amendment of 1970 as particularly harmful to human health. Concentrations have decreased markedly across the United States over the past 50 years in response to regulatory efforts, but continuing research on its deleterious effects have spurred further reductions in the legal threshold. The South Coast and San Joaquin Valley Air Basins of California remain the only two "extreme" ozone nonattainment areas in the United States. Further reductions of ozone in the West are complicated by significant background concentrations whose relative importance increases as domestic anthropogenic contributions decline and the national standards continue to be lowered. These background concentrations derive largely from uncontrollable sources including stratospheric intrusions, wildfires, and intercontinental transport. Taken together the exogenous sources complicate regulatory strategies and necessitate a much more precise understanding of the timing and magnitude of their contributions to regional air pollution. The California Baseline Ozone Transport Study was a field campaign coordinated across Northern and Central California during spring and summer 2016 aimed at observing daily variations in the ozone columns crossing the North American coastline, as well as the modification of the ozone layering downwind across the mountainous topography of California to better understand the impacts of background ozone on surface air quality in complex terrain.

Airborne estimates of greenhouse gas emissions are becoming more prevalent with the advent of rapid commercial development of trace gas instrumentation featuring increased measurement accuracy, precision, and frequency, and the swelling interest in the verification of current emission inventories. Multiple airborne studies have indicated that emission inventories may underestimate some hydrocarbon emission sources in US oil-and gas-producing basins. Consequently, a proper assessment of the accuracy of these airborne methods is crucial to interpreting the meaning of such discrepancies. We present a new method of sampling surface sources of any trace gas for which fast and precise measurements can be made and apply it to methane, ethane, and carbon dioxide on spatial scales of ĝ1/4 1000ĝ€m, where consecutive loops are flown around a targeted source region at multiple altitudes. Using Reynolds decomposition for the scalar concentrations, along with Gauss's theorem, we show that the method accurately accounts for the smaller-scale turbulent dispersion of the local plume, which is often ignored in other average mass balance methods. With the help of large eddy simulations (LES) we further show how the circling radius can be optimized for the micrometeorological conditions encountered during any flight. Furthermore, by sampling controlled releases of methane and ethane on the ground we can ascertain that the accuracy of the method, in appropriate meteorological conditions, is often better than 10ĝ€%, with limits of detection below 5ĝ€kgĝ€hĝ'1 for both methane and ethane. Because of the FAA-mandated minimum flight safe altitude of 150ĝ€m, placement of the aircraft is critical to preventing a large portion of the emission plume from flowing underneath the lowest aircraft sampling altitude, which is generally the leading source of uncertainty in these measurements. Finally, we show how the accuracy of the method is strongly dependent on the number of sampling loops and/or ti

Tracer flux ratio methodology was applied to airborne measurements to quantify methane (CH4) emissions from two dairy farms in central California during the summer. An aircraft flew around the perimeter of each farm measuring downwind enhancements of CH4 and a tracer species released from the ground at a known rate. Estimates of CH4 emission rates from this analysis were determined for whole sites and major sources within a site (animal housing and liquid manure lagoons). Whole-site CH4 flux rates for each farm, Dairy 1 (6108±821kgCH4dg-1, 95% confidence interval) and Dairy 2 (4018±456kgCH4dg-1, 95% confidence interval), closely resembled findings by established methods: ground-based tracer flux ratio and mass balance. Individual source emission rates indicate a greater fraction of the whole-site emissions come from liquid manure management than animal housing activity, similar to bottom-up estimates. Despite differences in altitude, we observed that the tracer release method gave consistent results when using ground or air platforms..

The San Joaquin Valley of California is known for excessive ozone air pollution owing to local production combined with terrain-induced flow patterns that channel air in from the highly populated San Francisco Bay area and stagnate it against the surrounding mountains. During the summer, ozone violations of the National Ambient Air Quality Standards (NAAQS) are notoriously common, with the San Joaquin Valley having an average of 115 violations of the current 70&ppb standard each year between 2012 and 2016. Because regional photochemical production peaks with actinic radiation, most studies focus on the daytime, and consequently the nocturnal chemistry and dynamics that contribute to these summertime high-ozone events are not as well elucidated. Here we investigate the hypothesis that on nights with a strong low-level jet (LLJ), ozone in the residual layer (RL) is more effectively mixed down into the nocturnal boundary layer (NBL) where it is subject to dry deposition to the surface, the rate of which is itself enhanced by the strength of the LLJ, resulting in lower ozone levels the following day. Conversely, nights with a weaker LLJ will sustain RLs that are more decoupled from the surface, retaining more ozone overnight, and thus lead to more fumigation of ozone the following mornings, giving rise to higher ozone concentrations the following afternoon. The relative importance of this effect, however, is strongly dependent on the net chemical overnight loss of Ox (here [Ox] ĝ‰i [O3] + [NO2]), which we show is highly uncertain, without knowing the ultimate chemical fate of the nitrate radical (NO3). We analyze aircraft data from a study sponsored by the California Air Resources Board (CARB) aimed at quantifying the role of RL ozone in the high-ozone events in this area. By formulating nocturnal scalar budgets based on pairs of consecutive flights (the first around midnight and the second just after sunrise the following day), we estimate the rate of vertical mixi