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Understanding the role of lake breeze in vertical ozone profiles using unmanned aerial systems at a shoreline location. Vertical profiles show gradients in ozone with higher ozone in areas of steep temperature inversion.

Surface-level ozone (O3) is a secondary air pollutant that has adverse effects on human health. In the troposphere, O3 is produced in complex cycles of photochemical reactions involving nitrogen oxides (NOx) and volatile organic compounds (VOCs). Determining if O3 levels will be decreased by lowering NOx emissions (“NOx-sensitive”), VOC emissions (“VOC-sensitive”), or both (“the transition zone”) can be done by using the formaldehyde (HCHO; a VOC species) to nitrogen dioxide (NO2; a component of NOx) concentration ratio (HCHO/NO2; “FNR”). Generally, lower FNR values indicate VOC sensitivity, while higher values indicate NOx sensitivity. Despite being a highly populated region with coastal O3 air quality issues, the Lake Michigan region in the United States, including the Chicago, Illinois, metropolitan area (CMA), remains relatively understudied, especially from the satellite perspective. In this work, we present the first study that utilizes TROPOspheric Monitoring Instrument (TROPOMI) satellite data over the Lake Michigan region from 2019–2021 to assess changes in O3 precursor levels and the inferred O3 chemistry sensitivity between (1) O3 season days and CMA O3 exceedance days and (2) weekdays and weekends. Higher NO2 vertical column densities (VCDs), HCHO VCDs, and FNR values are seen throughout the study domain on exceedance days, indicating generally more NOx-sensitive O3 chemistry. The largest change occurs in the areal extent of the transition zone, which decreases by 40 % during exceedance days. Major urban cores in the domain (e.g., Chicago, Illinois; Gary, Indiana; and Milwaukee, Wisconsin) remain VOC-sensitive on exceedance days as the higher NO2 VCDs in these areas counterbalance the regionally higher HCHO VCDs. Utilizing 10 m wind analysis data, we show that the lake breeze circulation is stronger on exceedance days. The strengthening of the lake breeze causes stronger convergence of the wind field along the southwestern Lake Michigan coastline, which can concentrate NO2 emissions originating in this area. This finding provides a possible explanation for the higher TROPOMI NO2 VCDs over the urban core of Chicago on exceedance days. Investigation of 2 m air temperature analysis data reveals that temperatures are higher on exceedance days, which explains the stronger lake breeze circulation and provides a possible cause for the higher TROPOMI HCHO VCDs over the entire region (due to increased temperature-dependent biogenic VOC emissions). Comparing weekdays and weekends, higher FNR values throughout much of the region indicate increasingly NOx-sensitive O3 chemistry on weekends. These changes are driven by lower NO2 VCDs in urban areas, particularly in Chicago, and higher HCHO VCDs in the southern part of the domain on weekends. Overall, our analyses suggest that VOC emissions controls in major urban areas and NOx emissions controls throughout the entire domain are necessary to decrease O3 levels in the Lake Michigan region.

We use the Weather Research and Forecasting with Chemistry (WRF-Chem) model with new implementations of GOES-16 wildfire emissions and plume rise based on fire radiative power (FRP) to interpret aerosol observations during the 2019 NASA-NOAA FIREX-AQ field campaign and perform model evaluations. We compare simulated aerosol concentrations and optical properties against observations of black carbon aerosol from the NOAA Single Particle Soot Photometer (NOAA-SP2), organic aerosol from the CU High-Resolution Aerosol Mass Spectrometer (HR-AMS), and aerosol backscatter coefficients from the high-spectral-resolution lidar (HSRL) system. This study focuses on the Williams Flats fire in Washington, which was repeatedly sampled during four science flights by the NASA DC-8 (3–8 August 2019). The emissions and plume-rise methodologies are implemented following NOAA's operational High-Resolution Rapid Refresh coupled with Smoke (HRRR-Smoke) forecasting model. In addition, new GOES-16 FRP-based diurnal cycle functions are developed and incorporated into WRF-Chem. The FIREX-AQ observations represented a diverse set of sampled environments ranging from fresh/aged smoke from the Williams Flats fire to remnants of plumes transported over long distances. The Williams Flats fire resulted in significant aerosol enhancements during 3–8 August 2019, which were substantially underestimated by the standard version of WRF-Chem. The simulated black carbon (BC) and organic carbon (OC) concentrations increased between a factor of 92–125 (BC) and a factor of 28–78 (OC) with the new implementation compared to the standard WRF-Chem version. These increases resulted in better agreement with the FIREX-AQ airborne observations for BC and OC concentrations (particularly for fresh smoke sampling phases) and aerosol backscatter coefficients. The model still showed a low bias in simulating the aerosol loadings observed in aged plumes from Williams Flats. WRF-Chem with the FRP-based plume rise simulated similar plume heights to the standard plume-rise model in WRF-Chem. The simulated plume heights (for both versions) compared well with estimated plume heights using the HSRL measurements. Therefore, the better agreement with observations was mainly driven by the higher emissions in the FRP-based version. The model evaluations also highlighted the importance of accurately accounting for the wildfire diurnal cycle and including adequate representation of the underlying chemical mechanisms, both of which could significantly impact model forecasting performance.

Ground-based thermodynamic and kinematic profilers were placed adjacent to the western shore of Lake Michigan at two sites as part of the 2017 Lake Michigan Ozone Study. The southern site near Zion, Illinois, hosted a microwave radiometer (MWR) and a sodar wind profiler, while the northern site in Sheboygan, Wisconsin, featured an Atmospheric Emitted Radiance Interferometer (AERI), a Doppler lidar, and a High Spectral Resolution Lidar (HSRL). Each site experienced several lake-breeze events during the experiment. Composite time series and time–height cross sections were constructed relative to the lake-breeze arrival time so that commonalities across events could be explored. The composited surface observations indicate that the wind direction of the lake breeze was consistently southeasterly at both sites regardless of its direction before the arrival of the lake-breeze front. Surface relative humidity increased with the arriving lake breeze, though this was due to cooler air temperatures as absolute moisture content stayed the same or decreased. The profiler observations show that the lake breeze penetrated deeper when the local environment was unstable and preexisting flow was weak. The cold air associated with the lake breeze remained confined to the lowest 200 m of the troposphere even if the wind shift was observed at higher altitudes. The evolution of the lake breeze corresponded well to observed changes in baroclinicity and calculated changes in circulation. Collocated observations of aerosols showed increases in number and mass concentrations after the passage of the lake-breeze front.

The Fires, Asian, and Stratospheric Transport–Las Vegas Ozone Study (FAST-LVOS) was conducted in May and June of 2017 to study the transport of ozone (O3) to Clark County, Nevada, a marginal non-attainment area in the southwestern United States (SWUS). This 6-week (20 May–30 June 2017) field campaign used lidar, ozonesonde, aircraft, and in situ measurements in conjunction with a variety of models to characterize the distribution of O3 and related species above southern Nevada and neighboring California and to probe the influence of stratospheric intrusions and wildfires as well as local, regional, and Asian pollution on surface O3 concentrations in the Las Vegas Valley (≈ 900 m above sea level, a.s.l.). In this paper, we describe the FAST-LVOS campaign and present case studies illustrating the influence of different transport processes on background O3 in Clark County and southern Nevada. The companion paper by Zhang et al. (2020) describes the use of the AM4 and GEOS-Chem global models to simulate the measurements and estimate the impacts of transported O3 on surface air quality across the greater southwestern US and Intermountain West. The FAST-LVOS measurements found elevated O3 layers above Las Vegas on more than 75 % (35 of 45) of the sample days and show that entrainment of these layers contributed to mean 8 h average regional background O3 concentrations of 50–55 parts per billion by volume (ppbv), or about 85–95 µg m−3. These high background concentrations constitute 70 %–80 % of the current US National Ambient Air Quality Standard (NAAQS) of 70 ppbv (≈ 120 µg m−3 at 900 m a.s.l.) for the daily maximum 8 h average (MDA8) and will make attainment of the more stringent standards of 60 or 65 ppbv currently being considered extremely difficult in the interior SWUS.

The finding of lymphadenopathy on physical examination and radiographically can suggest a wide range of differential diagnoses for patients, including a benign inflammatory process, infection, or malignancy. This article describes a patient with a history of Hodgkin lymphoma who developed postremission left axillary lymphadenopathy caused by deposits of tattoo ink in the node.

High-resolution simulations were performed to assess the impact of different parameterization schemes, surface initialization datasets, and analysis nudging on lower-tropospheric conditions near Lake Michigan. Simulations were run where climatological or coarse-resolution surface initialization datasets were replaced by high-resolution, real-time datasets depicting lake surface temperatures (SST), green vegetation fraction (GVF), and soil moisture and temperature (SOIL). Comparison of a baseline simulation employing a configuration similar to that used at the Environmental Protection Agency (“EPA”) to another simulation employing an alternative set of parameterization schemes (referred to as “YNT”) showed that the EPA configuration produced more accurate analyses on the outermost 12-km resolution domain, but that the YNT configuration was superior for higher-resolution nests. The diurnal evolution of the surface energy fluxes was similar in both simulations on the 12-km grid but differed greatly on the 1.3-km grid where the EPA simulation had much smaller sensible heat flux during the daytime and physically unrealistic ground heat flux. Switching to the YNT configuration led to substantial decreases in root mean square error for 2-m temperature and 2-m water vapor mixing ratio on the 1.3-km grid. Additional improvements occurred when the high-resolution satellite-derived surface datasets were incorporated into the modeling platform, with the SOIL dataset having the largest positive impact on temperature and water vapor. The GVF and SST datasets also produced more accurate temperature and water vapor analyses, but degradations in wind speed, especially when using the GVF dataset. The most accurate simulations were obtained when using the high-resolution SST and SOIL datasets and analysis nudging above 2 km AGL.

We evaluate two high-resolution Lake Michigan air quality simulations during the 2017 Lake Michigan Ozone Study campaign. These air quality simulations employ identical chemical configurations but use different input meteorology. The “EPA” configuration follows EPA recommended modeling practices, whereas the "YNT SSNG” employs different parameterization schemes and satellite-based inputs of sea surface temperatures, green vegetative fraction, and soil moisture and temperature. Overall, we find similar performance in model simulations of hourly and daily 8-hour maximum (MDA8) ozone, with the EPA and YNT_SSNG simulations showing biases of −13.31 and −13.54 ppbv, respectively during periods when the observed MDA8 was greater than 70 ppbv. However, for the two monitoring sites that observed high ozone events, the EPA simulation better matched observations at Sheboygan KA and the YNT_SSNG simulation better matched observations at Chiwaukee Prairie. We find differences between the two simulations are largest for column amounts of ozone precursors, particularly NO2. Across three high ozone events, the YNT_SSNG simulation has a lower column NO2 bias (0.17 × 1015 molecules/cm2) compared to the EPA simulation (0.35 × 1015 molecules/cm2). The YNT_SSNG simulation also has an advantage in better capturing the structure of the boundary layer and lake breeze during the June 2 high ozone event, although the timing of the lake breeze is about 3 hours too early. Our results are useful in informing an air quality modeling framework for the Lake Michigan area.

The atmospheric particle size distribution was measured at a rural lakeshore site (Zion, IL 42.468 N, 87.810 W) during the Lake Michigan Ozone Study (LMOS 2017) in May and June 2017. The full aerosol size distribution was continuously measured by two scanning mobility particle sizers and an aerodynamic particle sizer in the range of 1.02 to 8671 nm (electrical mobility diameter). The Zion site, 0.5 km from the lake, was one of two enhanced monitoring ground stations with collocated meteorology, remote sensing platforms, gravimetric filters, and gas-phase variables. Quantified size distributions of aerosols are important for understanding aerosol climate and health effects, for evaluation of models, and for understanding aerosol sources. Few studies have provided continuous, highly time-resolved, full particle size distribution near the shore of Lake Michigan, and none prior to this have extended measurements into the 1-3 nm size range. There were 14 identified ultrafine burst events, defined as particle growth from sub 10 nm to 25-100 nm, and all events began in the morning hours. Lake spray aerosol was investigated on June 5 when wave breaking conditions were sustained over the lake. The number distribution mode was 81 nm during the event; however, the amplitude of the particle size distribution dropped from 9000 cm-3 prior to the onset to 3000 cm-3 during and post event. Additional wind speed and direction analysis resulted in no identifiable pattern in the ultrafine particles when wind velocity exceed 4 m/s. Other measurement highlights include the mean number concentrations for 1-3 nm and 3-8761 nm were 1.80x104 cm-3 and 7998 cm-3 respectively, aerosol optical depth (0.084), reconstructed PM2.5 (6.4 μg m-3), reconstructed PM10 (7.9 μg m-3) and SO2 (0.32 ppb). Implications for future air quality management are also discussed.

The Lake Michigan Ozone Study 2017 (LMOS 2017) was a collaborative multiagency field study targeting ozone chemistry, meteorology, and air quality observations in the southern Lake Michigan area. The primary objective of LMOS 2017 was to provide measurements to improve air quality modeling of the complex meteorological and chemical environment in the region. LMOS 2017 science questions included spatiotemporal assessment of nitrogen oxides (NOx = NO + NO2) and volatile organic compounds (VOC) emission sources and their influence on ozone episodes; the role of lake breezes; contribution of new remote sensing tools such as GeoTASO, Pandora, and TEMPO to air quality management; and evaluation of photochemical grid models. The observing strategy included GeoTASO on board the NASA UC-12 aircraft capturing NO2 and formaldehyde columns, an in situ profiling aircraft, two ground-based coastal enhanced monitoring locations, continuous NO2 columns from coastal Pandora instruments, and an instrumented research vessel. Local photochemical ozone production was observed on 2 June, 9–12 June, and 14–16 June, providing insights on the processes relevant to state and federal air quality management. The LMOS 2017 aircraft mapped significant spatial and temporal variation of NO2 emissions as well as polluted layers with rapid ozone formation occurring in a shallow layer near the Lake Michigan surface. Meteorological characteristics of the lake breeze were observed in detail and measurements of ozone, NOx, nitric acid, hydrogen peroxide, VOC, oxygenated VOC (OVOC), and fine particulate matter (PM2.5) composition were conducted. This article summarizes the study design, directs readers to the campaign data repository, and presents a summary of findings.

Satellite observations of tropospheric NO2 columns can provide top-down observational constraints on emissions estimates of nitrogen oxides (NOx). Mass-balance-based methods are often applied for this purpose but do not isolate near-surface emissions from those aloft, such as lightning emissions. Here, we introduce an inverse modeling framework that couples satellite chemical data assimilation to a chemical transport model. In the framework, satellite-constrained emissions totals are inferred using model simulations with and without data assimilation in the iterative finite-difference mass-balance method. The approach improves the finite-difference mass-balance inversion by isolating the near-surface emissions increment. We apply the framework to separately estimate lightning and anthropogenic NOx emissions over the Northern Hemisphere for 2019. Using overlapping observations from the Ozone Monitoring Instrument (OMI) and the Tropospheric Monitoring Instrument (TROPOMI), we compare separate NOx emissions inferences from these satellite instruments, as well as the impacts of emissions changes on modeled NO2 and O3. OMI inferences of anthropogenic emissions consistently lead to larger emissions than TROPOMI inferences, attributed to a low bias in TROPOMI NO2 retrievals. Updated lightning NOx emissions from either satellite improve the chemical transport model's low tropospheric O3 bias. The combined lighting and anthropogenic emissions updates improve the model's ability to reproduce measured ozone by adjusting natural, long-range, and local pollution contributions. Thus, the framework informs and supports the design of domestic and international control strategies.

Airborne and ground-based Pandora spectrometer NOspan classCombining double low line"inline-formula"2/span column measurements were collected during the 2018 Long Island Sound Tropospheric Ozone Study (LISTOS) in the New York City/Long Island Sound region, which coincided with early observations from the Sentinel-5P TROPOspheric Monitoring Instrument (TROPOMI) instrument. Both airborne- and ground-based measurements are used to evaluate the TROPOMI NOspan classCombining double low line"inline-formula"2/span Tropospheric Vertical Column (TrVC) product v1.2 in this region, which has high spatial and temporal heterogeneity in NOspan classCombining double low line"inline-formula"2/span. First, airborne and Pandora TrVCs are compared to evaluate the uncertainty of the airborne TrVC and establish the spatial representativeness of the Pandora observations. The 171 coincidences between Pandora and airborne TrVCs are found to be highly correlated (span classCombining double low line"inline-formula"ir/i2Combining double low line/spanthinsp;0.92 and slope of 1.03), with the largest individual differences being associated with high temporal and/or spatial variability. These reference measurements (Pandora and airborne) are complementary with respect to temporal coverage and spatial representativity. Pandora spectrometers can provide continuous long-term measurements but may lack areal representativity when operated in direct-sun mode. Airborne spectrometers are typically only deployed for short periods of time, but their observations are more spatially representative of the satellite measurements with the added capability of retrieving at subpixel resolutions of 250thinsp;mthinsp;span classCombining double low line"inline-formula"×/spanthinsp;250thinsp;m over the entire TROPOMI pixels they overfly. Thus, airborne data are more correlated with TROPOMI measurements (span classCombining double low line"inline-formula"ir/i2Combining double low line0.96/span) than Pandora measurements are with TROPOMI (span classCombining double low line"inline-formula"ir/i2Combining double low line0.84/span). The largest outliers between TROPOMI and the reference measurements appear to stem from too spatially coarse a priori surface reflectivity (0.5span classCombining double low line"inline-formula"g /span) over bright urban scenes. In this work, this results during cloud-free scenes that, at times, are affected by errors in the TROPOMI cloud pressure retrieval impacting the calculation of tropospheric air mass factors. This factor causes a high bias in TROPOMI TrVCs of 4thinsp;%-11thinsp;%. Excluding these cloud-impacted points, TROPOMI has an overall low bias of 19thinsp;%-33thinsp;% during the LISTOS timeframe of June-September 2018. Part of this low bias is caused by coarse a priori profile input from the TM5-MP model; replacing thesespan idCombining double low line"page6114"/ profiles with those from a 12thinsp;km North American Model-Community Multiscale Air Quality (NAMCMAQ) analysis results in a 12thinsp;%-14thinsp;% increase in the TrVCs. Even with this improvement, the TROPOMI-NAMCMAQ TrVCs have a 7thinsp;%-19thinsp;% low bias, indicating needed improvement in a priori assumptions in the air mass factor calculation. Future work should explore additional impacts of a priori inputs to further assess the remaining low biases in TROPOMI using these datasets./.

We use the Weather Research and Forecasting with Chemistry (WRF-Chem) model with new implementations of GOES-16 fire radiative power (FRP) based wildfire emissions and plume-rise to interpret aerosol observations during the 2019 NASA-NOAA FIREX-AQ field campaign and perform model evaluations. We compare simulated aerosol concentrations and optical properties against observations of black carbon aerosol from the NOAA Single Particle Soot Photometer (NOAA-SP2), organic aerosol from the CU High Resolution Aerosol Mass Spectrometer (HR-AMS) and aerosol backscatter coefficients from the High Spectral Resolution Lidar (HSRL) system. This study focuses on the Williams Flats fire in Washington, which was repeatedly sampled during four science flights by the NASA DC-8 (August 3 – August 8, 2019). The emissions and plume-rise methodologies are implemented following NOAA’s operational High Resolution Rapid Refresh coupled with Smoke (HRRR-Smoke) forecasting model. In addition, new GOES-16 FRP based diurnal cycle functions are developed and incorporated in WRF-Chem. The FIREX-AQ observations represented a diverse set of sampled environments ranging from fresh/aged smoke from the Williams Flats fire to remnants of plumes transported over long distances. The Williams Flats fire resulted in significant aerosol enhancements during August 3–8, 2019, which were substantially underestimated by the standard version of WRF-Chem. The simulated BC and OC concentrations increased between 92 – 125 times (BC) and 28–78 times (OC) with the new implementation compared to the standard WRF-Chem version. These increases resulted in better agreement with the FIREX-AQ airborne observations for BC and OC concentrations (particularly for fresh smoke sampling phases) and aerosol backscatter coefficients. The model still showed a low bias in simulating the aerosol loadings observed in aged plumes from Williams Flats. WRF-Chem with the FRP-based plumerise simulated similar plume heights to the standard plumerise model in WRF-Chem. The simulated plume heights (for both versions) compared well with estimated plume heights using the HSRL measurements. Therefore, the improvements in the model simulation were mainly driven by the higher emissions in the FRP-based version. The model evaluations also highlighted the importance of accurately accounting for the wildfire diurnal cycle and including adequate representation of the underlying chemical mechanisms, both of which could significantly impact model forecasting performance.

The Fires, Asian, and Stratospheric Transport-Las Vegas Ozone Study (FAST-LVOS) was conducted in May and June of 2017 to study the transport of ozone (O3) to Clark County, Nevada, a marginal non-attainment area in the Southwestern U.S. (SWUS). This 6-week (20 May–30 June 2017) field campaign used lidar, ozonesonde, aircraft, and in-situ measurements in conjunction with a variety of models to characterize the distribution of O3 and related species above southern Nevada and neighbouring California, and to probe the influence of stratospheric intrusions, wildfires, and local, regional, and Asian pollution on surface O3 concentrations in Las Vegas and the surrounding area. In this paper, we describe the FAST-LVOS campaign and present case studies illustrating the influence of different transport processes on background O3 and air quality attainment in the SWUS. The measurements found elevated O3 layers above Las Vegas on more than 75 % (35 of 45) of the sample days, and show that entrainment of these layers contributed to mean 8-h average background O3 concentrations of 50–55 parts-per-billion by volume (ppbv) across southern Nevada. These background concentrations constitute 70–80 % of the current U.S. National Ambient Air Quality Standard (NAAQS) of 70 ppbv, and illustrate some of the challenges facing air quality managers tasked with O3 attainment in the SWUS during late spring and early summer. The companion paper by Zhang et al. (2020) describes the use of the AM4 and GEOS-Chem global models to estimate the impacts of transported O3 on surface air quality in the Southwestern U.S. and Intermountain West during the FAST-LVOS campaign.

Daytime onshore lake breezes are a critical factor controlling ozone abundance at coastal sites around Lake Michigan. Coastal counties along the western shore of Lake Michigan have historically observed high ozone episodes dating to the 1970s. We classified ozone episode days based on the extent or absence of the lake breeze (i.e., “inland”, “near-shore” or “no” lake breeze) to establish a climatology of these events. This work demonstrated variable gradients in ozone abundances based on these different types of meteorology, with the sharpest ozone concentration gradients on days with a near-shore lake breeze. On 76–82% of days in which ozone reached 70 ppb for at least 1 h, a lake breeze was present. Evidence of ozone gradients from multiple observation platforms during the 2017 Lake Michigan Ozone Study (LMOS 2017) are shown for two days with different depths of lake breezes.

The meso-scale meteorology of lake breezes along Lake Michigan impacts local observations of high ozone events. Previous manned aircraft and UAS observations have demonstrated non-uniform ozone concentrations within and above the marine layer over water and within shoreline environments. During the 2021 Wisconsin’s Dynamic Influence of Shoreline Circulations on Ozone (WiscoDISCO-21) campaign, two UAS platforms, a fixed-wing (University of Colorado RAAVEN) and a multirotor (Purdue University DJI M210), were used simultaneously to capture lake breeze during forecasted high ozone events at Chiwaukee Prairie State Natural Area in southeastern Wisconsin from May 21–26, 2021. The RAAVEN platform (data DOI: 10.5281/zenodo.5142491) measured temperature, humidity, and 3-D winds during 2-hour flights following two separate flight patterns up to 3 times per day at altitudes reaching 500 m above ground level. The M210 platform (data DOI: 10.5281/zenodo.5160346) measured vertical profiles of temperature, humidity and ozone during 15-minute flights up to 6 times per day at altitudes reaching 120 m above ground level (AGL) near to a WI-DNR ground monitoring station (AIRS ID: 55-059-0019). This campaign was conducted in conjunction with the Enhanced Ozone Monitoring plan from WI-DNR that included Doppler lidar wind profiler observations at the site (data DOI:10.5281/zenodo.5213039).

NASA deployed the GeoTASO airborne UV–visible spectrometer in May–June 2017 to produce high-resolution (approximately 250 m×250 m) gapless NO2 datasets over the western shore of Lake Michigan and over the Los Angeles Basin. The results collected show that the airborne tropospheric vertical column retrievals compare well with ground-based Pandora spectrometer column NO2 observations (r2=0.91 and slope of 1.03). Apparent disagreements between the two measurements can be sensitive to the coincidence criteria and are often associated with large local variability, including rapid temporal changes and spatial heterogeneity that may be observed differently by the sunward-viewing Pandora observations. The gapless mapping strategy executed during the 2017 GeoTASO flights provides data suitable for averaging to coarser areal resolutions to simulate satellite retrievals. As simulated satellite pixel area increases to values typical of TEMPO (Tropospheric Emissions: Monitoring Pollution), TROPOMI (TROPOspheric Monitoring Instrument), and OMI (Ozone Monitoring Instrument), the agreement with Pandora measurements degraded, particularly for the most polluted columns as localized large pollution enhancements observed by Pandora and GeoTASO are spatially averaged with nearby less-polluted locations within the larger area representative of the satellite spatial resolutions (aircraft-to-Pandora slope: TEMPO scale =0.88; TROPOMI scale =0.77; OMI scale =0.57). In these two regions, Pandora and TEMPO or TROPOMI have the potential to compare well at least up to pollution scales of 30×1015 molecules cm−2. Two publicly available OMI tropospheric NO2 retrievals are found to be biased low with respect to these Pandora observations. However, the agreement improves when higher-resolution a priori inputs are used for the tropospheric air mass factor calculation (NASA V3 standard product slope =0.18 and Berkeley High Resolution product slope =0.30). Overall, this work explores best practices for satellite validation strategies with Pandora direct-sun observations by showing the sensitivity to product spatial resolution and demonstrating how the high-spatial-resolution NO2 data retrieved from airborne spectrometers, such as GeoTASO, can be used with high-temporal-resolution ground-based column observations to evaluate the influence of spatial heterogeneity on validation results.

Airborne and ground-based Pandora spectrometer NO2 column measurements were collected during the 2018 Long Island Sound Tropospheric Ozone Study (LISTOS) in the New York City/Long Island Sound region, which coincided with early observations from the Sentinel-5P TROPOspheric Monitoring Instrument (TROPOMI) instrument. Both airborne- and ground-based measurements are used to evaluate the TROPOMI NO2 Tropospheric Vertical Column (TrVC) product v1.2 in this region, which has high spatial and temporal heterogeneity in NO2. First, airborne and Pandora TrVCs are compared to evaluate the uncertainty of the airborne TrVC and establish the spatial representativeness of the Pandora observations. The 171 coincidences between Pandora and airborne TrVCs are found to be highly correlated (r2 =0.92 and slope of 1.03), with the largest individual differences being associated with high temporal and/or spatial variability. These reference measurements (Pandora and airborne) are complementary with respect to temporal coverage and spatial representativity. Pandora spectrometers can provide continuous long-term measurements but may lack areal representativity when operated in direct-sun mode. Airborne spectrometers are typically only deployed for short periods of time, but their observations are more spatially representative of the satellite measurements with the added capability of retrieving at subpixel resolutions of 250m×250m over the entire TROPOMI pixels they overfly. Thus, airborne data are more correlated with TROPOMI measurements (r2 = 0.96) than Pandora measurements are with TROPOMI (r2 = 0.84). The largest outliers between TROPOMI and the reference measurements appear to stem from too spatially coarse a priori surface reflectivity (0.5°) over bright urban scenes. In this work, this results during cloud-free scenes that, at times, are affected by errors in the TROPOMI cloud pressure retrieval impacting the calculation of tropospheric air mass factors. This factor causes a high bias in TROPOMI TrVCs of 4%–11%. Excluding these cloud-impacted points, TROPOMI has an overall low bias of 19%–33% during the LISTOS timeframe of June–September 2018. Part of this low bias is caused by coarse a priori profile input from the TM5-MP model; replacing these profiles with those from a 12 km North American Model–Community Multiscale Air Quality (NAMCMAQ) analysis results in a 12%–14% increase in the TrVCs. Even with this improvement, the TROPOMI-NAMCMAQ TrVCs have a 7%–19% low bias, indicating needed improvement in a priori assumptions in the air mass factor calculation. Future work should explore additional impacts of a priori inputs to further assess the remaining low biases in TROPOMI using these datasets.

Desert dust as a source of iron and other micronutrients is recognized to fertilize oceans, but little attention has been paid to dust as a source of iodine. Empirical observations find iodate on dust measured during ship cruises downwind of the Sahara desert. However, it remains unclear whether iodine in dust is the result of marine iodine uptake on dust during transport in the marine boundary layer, or whether such iodine accumulates over geological time scales, and is emitted together with dust. Significant enhancements of iodine have been observed in Sahara dust events in form of methyl iodide (CH3I) and iodine monoxide (IO) radicals, but atmospheric models currently do not consider dust as a source of iodine. Furthermore, dust plumes are often accompanied by significant ozone loss, which is commonly attributed to reactive uptake of O3 and other odd oxygen species (i.e., N2O5, HNO3) on dust surfaces. However, laboratory experiments struggle to reproduce the large reactive uptake coefficients needed to explain field observations, and do not consider iodine chemistry. We present evidence that dust induced "mini ozone holes" in the remote (Southern Hemisphere) lower free troposphere west of South America (TORERO field campaign) are largely the result of gas-phase iodine chemistry in otherwise unpolluted (low NOx) dust layers that originate from the Atacama and Sechura Deserts. Ozone concentrations inside these elevated dust layers are often 10-20 ppb, and as low as 3 ppb, and influence entrainment of low ozone air from aloft into the marine boundary layer. Ozone depletion is found to be widespread, extending up to 6km altitude, and thousands of kilometers along the coast. Elevated IO radical concentrations inside decoupled dust layers are higher than in the marine boundary layer, and serve as a source of iodine, and vigorous ozone sink following entrainment to the marine boundary layer. The implications for our perception of iodine sources, surface air quality, oxidative capacity, and climate are briefly discussed.

Tuberous sclerosis complex (TSC) is a genetic disorder that affects multiple organ systems but often goes unrecognized, and a delay in diagnosis can lead to multiple complications. Healthcare professionals should be educated on the many signs and symptoms associated with the disorder, know how to treat them symptomatically, and recommend routine screening to assess for complications. Correctly identifying, diagnosing, and treating TSC can give patients a better quality of life and prevent further complications associated with the disorder.

A summary of the Scanning High-resolution Interferometer Sounder (S-HIS) observations from the FIREX-AQ (Fire Influence on Regional to Global Environments and Air Quality) field campaign is presented.

The Lake Michigan Ozone Study 2017 (LMOS 2017) in May and June 2017 enabled study of transport, emissions, and chemical evolution related to ozone air pollution in the Lake Michigan airshed. Two highly instrumented ground sampling sites were part of a wider sampling strategy of aircraft, shipborne, and ground-based mobile sampling. The Zion, Illinois site (on the coast of Lake Michigan, 67 km north of Chicago) was selected to sample higher NOx air parcels having undergone less photochemical processing. The Sheboygan, Wisconsin site (on the coast of Lake Michigan, 211 km north of Chicago) was selected due to its favorable location for observation of photochemically aged plumes during ozone episodes involving southerly winds with lake breeze. The study encountered elevated ozone during three multiday periods. Daytime ozone episode concentrations at Zion were 60 ppb for ozone, 3.8 ppb for NOx, 1.2 ppb for nitric acid, and 8.2 µg/m3 for fine particulate matter. At Sheboygan daytime ozone episode concentrations were 60 ppb for ozone, 2.5 ppb for NOx, and 2.9 ppb for NOy. To facilitate informed use of the LMOS 2017 data repository, we here present comprehensive site description, including airmass influences during high ozone periods of the campaign, overview of meteorological and pollutant measurements, analysis of continuous emission monitor data from nearby large point sources, and characterization of local source impacts from vehicle traffic, large point sources, and rail. Consistent with previous field campaigns and the conceptual model of ozone episodes in the area, trajectories from the southwest, south, and lake breeze trajectories (south or southeast) were overrepresented during pollution episodes. Local source impacts from vehicle traffic, large point sources, and rail were assessed and found to represent less than about 15% of typical concentrations measured. Implications for model-observation comparison and design of future field campaigns are discussed. Implication StatementThe Lake Michigan Ozone Study 2017 (LMOS 2017) was conducted along the western shore of Lake Michigan, and involved two well-instrumented coastal ground sites (Zion, IL, and Sheboygan, WI). LMOS 2017 data is publicly available, and this paper provides detailed site characterization and measurement summary to enable informed use of repository data. Minor local source impacts were detected but were largely confined to nighttime conditions of less interest for ozone episode analysis and modeling. The role of these sites in the wider field campaign and their detailed description facilitates future campaign planning, informed data repository use, and model-observation comparison. Implication Statement The Lake Michigan Ozone Study 2017 (LMOS 2017) was conducted along the western shore of Lake Michigan, and involved two well-instrumented coastal ground sites (Zion, IL, and Sheboygan, WI). LMOS 2017 data is publicly available, and this paper provides detailed site characterization and measurement summary to enable informed use of repository data. Minor local source impacts were detected but were largely confined to nighttime conditions of less interest for ozone episode analysis and modeling. The role of these sites in the wider field campaign and their detailed description facilitates future campaign planning, informed data repository use, and model-observation comparison.

Abundant NO2 column measurements from airborne and ground-based Pandora spectrometers were collected as part of the 2018 Long Island Sound Tropospheric Ozone Study (LISTOS) in the New York City/Long Island Sound region and coincided with early measurements from the Sentinel-5P TROPOMI instrument. Both airborne- and ground-based measurements are used to evaluate the TROPOspheric Monitoring Instrument (TROPOMI) NO2 Tropospheric Vertical Column (TrVC) product v1.2 in this region, which has high spatial and temporal heterogeneity in NO2. First, airborne and Pandora TrVCs are compared to evaluate the uncertainty of the airborne TrVC and establish the spatial representativeness of the Pandora observations. The 171 coincidences between Pandora and airborne TrVCs are found to be highly correlated (r2=0.92 and slope of 1.03) with the biggest individual differences being associated with high temporal and/or spatial variability. These reference measurements (Pandora and airborne) are complementary with respect to temporal coverage and spatial representivity. Pandora spectrometers can provide continuous long-term measurements but may lack areal representivity when operated in direct-sun mode. Airborne spectrometers are typically only deployed for short periods of time, but their observations are more spatially representative of the satellite measurements with the added capability of retrieving at subpixel resolutions of 250 m × 250 m over the entire TROPOMI pixels they overfly. Thus, airborne data are more correlated with TROPOMI measurements (r2=0.96) than Pandora measurements are with TROPOMI (r2=0.84). The largest outliers between TROPOMI and the reference measurements are caused by errors in the TROPOMI retrieval of cloud pressure impacting the calculation of tropospheric air mass factors in cloud-free scenes. This factor causes a high bias in TROPOMI TrVCs of 4–11 %. Excluding these cloud-impacted points, TROPOMI has an overall low bias of 19–33% during the LISTOS timeframe of June–September 2018. Part of this low bias is caused by coarse a priori profile input from TM5-MP model; replacing these profiles with those from a 12 km NAMCMAQ analysis results in a 12–14 % increase in the TrVCs. Even with this improvement, the TROPOMI-NAMCMAQ TrVCs have a 7–19 % low bias, indicating needed improvement in a priori assumptions in the air mass factor calculation. Future work should explore additional impacts of a priori inputs to further assess the remaining low biases in TROPOMI using these datasets.

Ambient air pollution from ozone and fine particulate matter is associated with premature mortality. As emissions from one continent influence air quality over others, changes in emissions can also influence human health on other continents. We estimate global air-pollution-related premature mortality from exposure to PM2.5 and ozone and the avoided deaths due to 20 % anthropogenic emission reductions from six source regions, North America (NAM), Europe (EUR), South Asia (SAS), East Asia (EAS), Russia–Belarus–Ukraine (RBU), and the Middle East (MDE), three global emission sectors, power and industry (PIN), ground transportation (TRN), and residential (RES), and one global domain (GLO), using an ensemble of global chemical transport model simulations coordinated by the second phase of the Task Force on Hemispheric Transport of Air Pollutants (TF HTAP2), and epidemiologically derived concentration response functions. We build on results from previous studies of TF HTAP by using improved atmospheric models driven by new estimates of 2010 anthropogenic emissions (excluding methane), with more source and receptor regions, new consideration of source sector impacts, and new epidemiological mortality functions. We estimate 290 000 (95 % confidence interval (CI): 30 000, 600 000) premature O3-related deaths and 2.8 million (0.5 million, 4.6 million) PM2.5-related premature deaths globally for the baseline year 2010. While 20 % emission reductions from one region generally lead to more avoided deaths within the source region than outside, reducing emissions from MDE and RBU can avoid more O3-related deaths outside of these regions than within, and reducing MDE emissions also avoids more PM2.5-related deaths outside of MDE than within. Our findings that most avoided O3-related deaths from emission reductions in NAM and EUR occur outside of those regions contrast with those of previous studies, while estimates of PM2.5-related deaths from NAM, EUR, SAS, and EAS emission reductions agree well. In addition, EUR, MDE, and RBU have more avoided O3-related deaths from reducing foreign emissions than from domestic reductions. For six regional emission reductions, the total avoided extra-regional mortality is estimated as 6000 (−3400, 15 500) deaths per year and 25 100 (8200, 35 800) deaths per year through changes in O3 and PM2.5, respectively. Interregional transport of air pollutants leads to more deaths through changes in PM2.5 than in O3, even though O3 is transported more on interregional scales, since PM2.5 has a stronger influence on mortality. For NAM and EUR, our estimates of avoided mortality from regional and extra-regional emission reductions are comparable to those estimated by regional models for these same experiments. In sectoral emission reductions, TRN emissions account for the greatest fraction (26–53 % of global emission reduction) of O3-related premature deaths in most regions, in agreement with previous studies, except for EAS (58 %) and RBU (38 %) where PIN emissions dominate. In contrast, PIN emission reductions have the greatest fraction (38–78 % of global emission reduction) of PM2.5-related deaths in most regions, except for SAS (45 %) where RES emission dominates, which differs with previous studies in which RES emissions dominate global health impacts. The spread of air pollutant concentration changes across models contributes most to the overall uncertainty in estimated avoided deaths, highlighting the uncertainty in results based on a single model. Despite uncertainties, the health benefits of reduced intercontinental air pollution transport suggest that international cooperation may be desirable to mitigate pollution transported over long distances.

Military medicine has made significant advancements in decreasing mortality by addressing the lethal triad - metabolic acidosis, coagulopathy, and hypothermia. However, casualties are still succumbing to injury. Recent conflict zones have led to the development of remarkable life-saving innovations, including the management of compressible hemorrhage and whole blood transfusions. Nevertheless, hypothermia prevention and treatment techniques remain relatively unchanged. Hypothermia prevention is anticipated to become more critical in future operations due to a predicted increase in evacuation times and reliance on Prolonged Casualty Care (PCC). This is likely secondary to increasingly distanced battlespaces and the mobility challenges of operating in semi-/non-permissive environments. Innovation is essential to combat this threat via active airway rewarming in the vulnerable patient. Thus, we propose the development, fabrication, and efficacy testing of a device in which we estimate being able to control temperature and humidity at physiologic levels in the PCC setting and beyond.