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The Soberanes Fire burned 53,470 ha (132,127 acres) along the central California coast between 22 July and 12 October 2016, generating dense smoke and a variety of gaseous compounds that drifted eastward into the San Joaquin Valley Air Basin (SJVAB), an “extreme” nonattainment area for ozone (O3). These gases included nitrogen oxides (NOx) and volatile organic compounds, the photochemical precursors of O3. The fire started during the California Baseline Ozone Transport Study, a field campaign that brought aircraft, surface, and remote sensing measurements of O3 and related species to central California. In this paper, we use the California Baseline Ozone Transport Study measurements to assess the impact of the Soberanes Fire on ozone and particulate air quality in the SJVAB. We focus our analysis on 27 July to 2 August when the smoke haze was heaviest and the highest O3 concentrations in the SJVAB during 2016 were recorded. Our analyses suggest that while 40 to 60 ppbv of fire-generated O3 was transported to the eastern SJVAB in the 1- to 3-km-altitude range, relatively little smoke or fire-generated O3 reached the surface in the Visalia area.

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.

The California Baseline Ozone Transport Study (CABOTS) was conducted in the late spring and summer of 2016 to investigate the influence of long-range transport and stratospheric intrusions on surface ozone (O3) concentrations in California with emphasis on the San Joaquin Valley (SJV), one of two extreme ozone non-attainment areas in the US. One of the major objectives of CABOTS was to characterize the vertical distribution of O3 and aerosols above the SJV to aid in the identification of elevated transport layers and assess their surface impacts. To this end, the NOAA Earth System Research Laboratory (ESRL) deployed the Tunable Optical Profiler for Aerosol and oZone (TOPAZ) mobile lidar to the Visalia Municipal Airport (36.315 N, 119.392E) in the central SJV between 27 May and 7 August 2016. Here we compare the TOPAZ ozone retrievals with co-located in situ surface measurements and nearby regulatory monitors and also with airborne in situ measurements from the University of California at Davis-Scientific Aviation (SciAv) Mooney and NASA Alpha Jet Atmospheric eXperiment (AJAX) research aircraft. Our analysis shows that the lidar and aircraft measurements agree, on average to within 5ppbv, the sum of their stated uncertainties of 3 and 2ppbv, respectively.

The Tropospheric Ozone Lidar Network (TOLNet) was used to validate retrievals of ozone (O 3) profiles in the troposphere from the TROPOspheric Monitoring Instrument (TROPOMI) ultraviolet (UV), Cross-track Infrared Sounder (CrIS) infrared (IR), and a combined UV + IR wavelength retrieval from TROPOMI/CrIS. Observations from six separate ground-based lidar systems and various locations of ozonesondes distributed throughout North America and in the Netherlands were used to quantify systematic bias and random errors for each satellite retrieval. Furthermore, TOLNet data were used to intercompare idealized UV, IR, and UV + IR convolved lidar profiles of O 3 in the troposphere during case studies representative of high-O 3 events. This study shows that the improved sensitivity and vertical resolution in UV + IR retrievals in the middle- and upper-troposphere resulted in tropospheric degree of freedom (DOF) values ∼ 33 % higher compared to UV- and IR-only retrievals. The increased DOFs in the UV + IR retrievals allowed for improved reproduction of mid- and upper-tropospheric O 3 enhancements and, to a lesser degree, near-surface pollution enhancements compared to single-wavelength satellite products. The validation of O 3 profiles in the troposphere retrieved with the UV-only, IR-only, and UV + IR Tikhonov regularised Ozone Profile retrievAl with SCIATRAN (TOPAS) algorithm developed at the Institute for Environmental Physics, University of Bremen, demonstrated the utility of using TOLNet as a satellite evaluation data set. TOPAS UV-only, IR-only, and UV + IR wavelength retrievals had systematic biases, quantified with normalized mean bias, throughout the troposphere of 11.2 ppb (22.1 %), -1.7 ppb (-0.3 %), and 3.5 ppb (7.8 %), respectively, which meet the tropospheric systematic bias requirements defined by the science teams for the TROPOMI and CrIS sensors. The primary drivers of systematic bias were determined to be solar zenith angle, surface albedo, and cloud fraction. Random errors, representative of uncertainty in the retrievals and quantified by root mean squared errors (RMSEs), were large for all three retrievals, with UV-only, IR-only, and UV + IR wavelength retrievals having RMSEs throughout the troposphere of 17.4 ppb (19.8 % of mean tropospheric column values), 10.5 ppb (12.6 % of mean tropospheric column values), and 14.0 ppb (14.6 % of mean tropospheric column values), respectively. TOPAS UV-only profiles did not meet the uncertainty requirements defined for TROPOMI for the troposphere; however, CrIS IR-only retrievals did meet the uncertainty requirements defined by this mission. The larger random errors reflect the challenge of retrieving daily O 3 profiles due to the limited sensitivity and vertical resolution of these retrievals in the troposphere. Tropospheric systematic biases and random error were lower in IR-only and combined UV + IR retrievals compared to UV-only products due to the increased sensitivity in the troposphere allowing the retrievals to deviate further from the a priori profiles. Observations from TOLNet demonstrated that the performance of the three satellite products varied by season and altitude in the troposphere. TOLNet was shown to result in similar validation statistics compared to ozonesonde data, which are a commonly used satellite evaluation data source, demonstrating that TOLNet is a sufficient source of satellite O 3 profile validation data in the troposphere, which is critical as this data source is the primary product identified for the tropospheric O 3 validation of the recently launched Tropospheric Emissions: Monitoring of Pollution (TEMPO) mission. [ABSTRACT FROM AUTHOR]

The Tropospheric Ozone Lidar Network (TOLNet) was applied to validate retrievals of ozone (O3) profiles in the troposphere from the TROPOspheric Monitoring Instrument (TROPOMI) ultraviolet (UV), Cross-track Infrared Sounder (CrIS) infrared (IR), and a combined UV+IR wavelength retrieval from TROPOMI/CrIS. Observations from six separate ground-based lidar systems and various locations of ozonesondes distributed throughout North America and Europe were applied to quantify systematic bias and random errors for each satellite retrieval. Furthermore, TOLNet data were used to intercompare idealized UV, IR, and UV+IR convolved profiles of O3 in the troposphere during case studies representative of high O3 events. This study shows that the combination of wavelengths in satellite retrievals (i.e., UV+IR) increases the sensitivity and vertical resolution of the retrievals of O3 in the troposphere compared to single-wavelength products. The improved sensitivity and vertical resolution in UV+IR retrievals in the middle- and upper-troposphere resulted in tropospheric degree of freedom (DOF) values ~33 % higher compared to UV- and IR-only retrievals. The increased DOFs in the UV+IR retrievals allowed for improved reproduction of mid- and upper-tropospheric O3 enhancements, and to a lesser degree near-surface pollution enhancements, compared to single wavelength satellite products. The validation of O3 profiles in the troposphere retrieved with the UV-only, IR-only, and UV+IR Tikhonov regularised Ozone Profile retrievAl with SCIATRAN (TOPAS) algorithm developed at the Institute for Environmental Physics, University of Bremen demonstrated the utility of using TOLNet as a satellite evaluation data set. TOPAS UV-only, IR-only, and UV+IR wavelength retrievals had systematic biases throughout the troposphere of 11.2 ppb (22.1 %), -1.7 ppb (-0.3 %), and 3.5 ppb (7.8 %), respectively, which meet the tropospheric systematic bias requirements of TROPOMI and CrIS. The primary drivers of systematic bias were determined to be the a priori vertical profile shape, solar zenith angle, and surface albedo. Random errors, representative of uncertainty in the retrievals, were large for all three retrievals with UV-only, IR-only, and UV+IR wavelength retrievals having root mean squared errors (RMSE) throughout the troposphere of 17.4 ppb (19.8 % of mean tropospheric column values), 10.5 ppb (12.6 % of mean tropospheric column values), and 14.0 ppb (14.6 % of mean tropospheric column values), respectively. TOPAS UV-only profiles did not meet the uncertainty requirements defined for TROPOMI for the troposphere; however, CrIS IR-only retrievals did meet the uncertainty requirements defined by this mission. The larger random biases reflect the challenge of retrieving daily O3 profiles due to the limited sensitivity and vertical resolution of these retrievals in the troposphere. Tropospheric systematic biases and random error were lower in IR-only and combined UV+IR retrievals compared to UV-only products due to the increased sensitivity in the troposphere allowing the retrievals to deviate further from the a priori profiles. Consistent daily observations from TOLNet demonstrated that the performance of the three satellite products varied by season and altitude in the troposphere. TOLNet was shown in this study to be a sufficient source of satellite O3 profile validation data in the troposphere which is critical as this data source is the primary product identified for the tropospheric O3 validation of the recently-launched Tropospheric Emissions: Monitoring of Pollution (TEMPO) mission. [ABSTRACT FROM AUTHOR]

The Tropospheric Ozone Lidar Network (TOLNet) is a unique network of lidar systems that measure atmospheric profiles of ozone and aerosols, to contribute to air-quality studies, atmospheric modeling, and satellite validation efforts. The accurate characterization of these lidars is of critical interest, and is necessary to determine cross-instrument calibration uniformity. From July to August 2014, three lidars, the TROPospheric OZone (TROPOZ) lidar, the Tunable Optical Profiler for Aerosol and oZone (TOPAZ) lidar, and the Langley Mobile Ozone Lidar (LMOL), of TOLNet participated in the “Deriving Information on Surface conditions from Column and Vertically Resolved Observations Relevant to Air Quality” (DISCOVER-AQ) mission and the “Front Range Air Pollution and Photochemistry Éxperiment” (FRAPPÉ) to measure sub-hourly ozone variations from near the surface to the top of the troposphere. Although large differences occur at few individual altitudes in the near field and far field range, the TOLNet lidars agree with each other within ±4%. These results indicate excellent measurement accuracy for the TOLNet lidars that is suitable for use in air-quality and ozone modeling efforts.

The Ozone Profiling Atmospheric Lidar is a scanning four-wavelength ultraviolet differential absorption lidar that measures tropospheric ozone and aerosols. Derived profiles from the lidar data include ozone concentration, aerosol extinction, and calibrated aerosol backscatter. Aerosol calibrations assume a clear air region aloft. Other products include cloud base heights, aerosol layer heights, and scans of particulate plumes from aircraft. The aerosol data range from 280 m to 12 km with 5 m range resolution, while the ozone data ranges from 280 m to about 12 km with 100 m resolution. In horizontally homogeneous atmospheres, data from multiple-elevation angles is combined to reduce the minimum altitude of the aerosol and ozone profiles to about 20 m. The lidar design, the characterization of the photomultiplier tubes, ozone and aerosol analysis techniques, and sample data are described. Also discussed is a double-gating technique to shorten the gated turn-on time of the photomultiplier tubes, and thereby reduce the detection of background light and the outgoing laser pulse. OCIS codes: 010.3640, 010.4950, 040.5250, 280.1100, 280.1120, 280.1910.

Ozone lidars measure continuous, high-resolution ozone profiles critical for process studies and for satellite validation in the lower troposphere. However, the effectiveness of lidar validation by using single-station data is limited. Recently, NASA initiated an interagency ozone lidar observation network under the name TOLNet to promote cooperative multiple-station ozone-lidar observations to provide highly timeresolved (few minutes) tropospheric-ozone vertical profiles useful for air-quality studies, model evaluation, and satellite validation. This article briefly describes the concept, stations, major specifications of the TOLNet instruments, and data archiving.

The California Baseline Ozone Transport Study (CABOTS) was conducted in the late spring and summer of 2016 to investigate the influence of long-range transport and stratospheric intrusions on surface ozone (O3) concentrations in California with emphasis on the San Joaquin Valley (SJV), one of two extreme ozone non-attainment areas in the U.S. One of the major objectives of CABOTS was to characterize the vertical distribution of O3 and aerosols above the SJV to aid in the identification of elevated transport layers and assess their surface impacts. To this end, the NOAA Earth System Research Laboratory (ESRL) deployed the Tunable Optical Profiler for Aerosol and oZone (TOPAZ) mobile lidar to the Visalia Municipal Airport (36.315° N, -119.392° E) in the central SJV between 27 May and 7 August 2016. Here we compare the TOPAZ ozone and backscatter measurements with co-located in-situ surface measurements and nearby regulatory monitors, and to airborne measurements from the University of California at Davis/Scientific Aviation Mooney and NASA Alpha Jet Atmospheric eXperiment (AJAX) research aircraft. Our analysis shows excellent agreement between the lidar and in-situ measurements, lending confidence to the use of these data sets for more detailed analyses. [ABSTRACT FROM AUTHOR]

Biomass burning plumes containing aerosols from forest fires can be transported long distances, which can ultimately impact climate and air quality in regions far from the source. Interestingly, these fires can inject aerosols other than smoke into the atmosphere, which very few studies have evidenced. Here, we demonstrate a set of case studies of long-range transport of mineral dust aerosols in addition to smoke from numerous forest fires in the Pacific Northwest to Colorado, U.S. These aerosols were detected in Boulder, Colorado along the Front Range using Beta-ray attenuation and energy dispersive X-ray fluorescence spectroscopy, and corroborated with satellite-borne lidar observations of smoke and dust. Further, we examined the transport pathways of these aerosols using air mass trajectory analysis and regional and synoptic scale meteorological dynamics. Three separate events with poor air quality and increased mass concentrations of metals from biomass burning (S and K) and minerals (Al, Si, Ca, Fe, and Ti) occurred due to the introduction of smoke and dust from regional and synoptic scale winds. Cleaner time periods with good air quality and lesser concentrations of biomass burning and mineral metals between the haze events were due to the advection of smoke and dust away from the region. Dust and smoke present in biomass burning haze can have diverse impacts on visibility, health, cloud formation, and surface radiation. Thus, it is important to understand how aerosol populations can be influenced by long-range transported aerosols, particularly those emitted from large source contributors such as forest fires. [ABSTRACT FROM AUTHOR]

Abstract: Airborne and surface measurements of ozone (O3) during the Texas Air Quality Study campaigns in 2000 and 2006 (TexAQS 2000 and TexAQS 2006) were used to investigate the relationship between maximum daily O3 and the vector-averaged wind speed , calculated from radar wind profiler data, in the lower atmospheric boundary layer (BL). Both the maximum daily O3 and the peak “add-on” O3 contribution (calculated as the maximum minus the background values) from the Houston area showed a strong correlation (r∼0.7–0.9) with both the reciprocal of this wind speed −1, and the wind speed itself. Data from airborne platforms produced higher correlations in general than surface-measured values. Except for special cases where O3 was measured close to source activity in a location where the BL depth h was suppressed, peak daily ozone concentrations were not strongly correlated with h, and attempts to include 1/h dependence with −1 degraded the correlations—indicating that in general, h was not a strong predictor for maximum daily O3. Inclusion of daily maximum temperature in the regression analysis also failed to improve the correlations significantly. The high correlations for wind speed thus showed that was the meteorological variable most strongly associated with peak daily O3 concentrations. The best-fit regression line of peak daily O3 vs. for the 2000 data lay above the line for 2006 for wind speeds less than 5 m s−1, the difference increasing as the wind speeds weakened. This six-year decrease in O3 concentrations for the weakest-wind, most polluted days suggests that control strategies implemented between 2000 and 2006 may be producing beneficial effects, especially on the most polluted days. [ABSTRACT FROM AUTHOR]