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The lake breeze circulation along Lake Michigan is associated with high tropospheric ozone concentrations at shoreline locations. The 2021 Wisconsin's Dynamic Influence of Shoreline Circulation on Ozone (WiscoDISCO-21) campaign involved atmospheric measurements over Chiwaukee Prairie State Natural Area in Southeastern Wisconsin from May 21–26, 2021. Three different platforms, two uncrewed aerial systems (UAS) and a Doppler lidar instrument, were used to collect data on this campaign, supplemented by a ground-based Wisconsin DNR maintained regulatory monitor at the site. A Purdue University M210 multirotor copter, and the University of Colorado RAAVEN fixed-wing aircraft were flown in coordination. Using data from the ground station, RAAVEN and onsite lidar, lake breezes were detected on several days of the campaign. The longest sustained lake breezes during the campaign were detected on May 22, 2021, from 17:00–21:38 UTC and on May 24, 2021, from 14:24–22:51 UTC. The presence of the lake breezes correlated with detected temperature inversions measured from the RAAVEN and high ozone events measured from the M210. Lake breezes were investigated with their relationship to vertical profiles measured on the UAS, ozone concentrations, and marine boundary layer height observed with Doppler lidar to demonstrate a multi-layered lower atmosphere. A buoyant internal boundary layer was observed over land from 40–100 m AGL below highest ozone concentrations. Marine layer extent was investigated through minimum buoyancy and Richardson number analysis, showing limited vertical mixing at altitudes up to 200 m AGL, below easterly lake breeze circulation patterns extending upward to 400 m AGL in the late day. 

Abstract. The mesoscale meteorology of lake breezes along Lake Michiganimpacts local observations of high-ozone events. Previous manned aircraftand UAS observations have demonstrated non-uniform ozone concentrationswithin and above the marine layer over water and within shorelineenvironments. During the 2021 Wisconsin's Dynamic Influence of ShorelineCirculations on Ozone (WiscoDISCO-21) campaign, two UAS platforms, afixed-wing (University of Colorado RAAVEN) and a multirotor (PurdueUniversity DJI M210), were used simultaneously to capture lake breeze duringforecasted high-ozone events at Chiwaukee Prairie State Natural Area insoutheastern Wisconsin from 21–26 May 2021​​​​​​​. The RAAVEN platform (data DOI:https://doi.org/10.5281/zenodo.5142491, de Boer et al., 2021) measured temperature, humidity, and 3-D winds during2 h flights following two separate flight patterns up to three times per dayat altitudes reaching 500 m above ground level (a.g.l.). The M210 platform (data DOI: https://doi.org/10.5281/zenodo.5160346, Cleary et al., 2021a) measured vertical profiles of temperature, humidity,and ozone during 15 min flights up to six times per day at altitudesreaching 120 ma.g.l. near a Wisconsin DNR ground monitoringstation (AIRS ID: 55-059-0019). This campaign was conducted in conjunctionwith the Enhanced Ozone Monitoring plan from the Wisconsin DNR that included Dopplerlidar wind profiler observations at the site (dataDOI: https://doi.org/10.5281/zenodo.5213039, Cleary et al., 2021b). 

Iodine is an atmospheric trace element emitted from oceans that efficiently destroys ozone (O 3 ). Low O 3 in airborne dust layers is frequently observed but poorly understood. We show that dust is a source of gas-phase iodine, indicated by aircraft observations of iodine monoxide (IO) radicals inside lofted dust layers from the Atacama and Sechura Deserts that are up to a factor of 10 enhanced over background. Gas-phase iodine photochemistry, commensurate with observed IO, is needed to explain the low O 3 inside these dust layers (below 15 ppbv; up to 75% depleted). The added dust iodine can explain decreases in O 3 of 8% regionally and affects surface air quality. Our data suggest that iodate reduction to form volatile iodine species is a missing process in the geochemical iodine cycle and presents an unrecognized aeolian source of iodine. Atmospheric iodine has tripled since 1950 and affects ozone layer recovery and particle formation. 

The NOAA/NASA Fire Influence on Regional to Global Environments and Air Quality (FIREX‐AQ) experiment was a multi‐agency, inter‐disciplinary research effort to: (a) obtain detailed measurements of trace gas and aerosol emissions from wildfires and prescribed fires using aircraft, satellites and ground‐based instruments, (b) make extensive suborbital remote sensing measurements of fire dynamics, (c) assess local, regional, and global modeling of fires, and (d) strengthen connections to observables on the ground such as fuels and fuel consumption and satellite products such as burned area and fire radiative power. From Boise, ID western wildfires were studied with the NASA DC‐8 and two NOAA Twin Otter aircraft. The high‐altitude NASA ER‐2 was deployed from Palmdale, CA to observe some of these fires in conjunction with satellite overpasses and the other aircraft. Further research was conducted on three mobile laboratories and ground sites, and 17 different modeling forecast and analyses products for fire, fuels and air quality and climate implications. From Salina, KS the DC‐8 investigated 87 smaller fires in the Southeast with remote and in‐situ data collection. Sampling by all platforms was designed to measure emissions of trace gases and aerosols with multiple transects to capture the chemical transformation of these emissions and perform remote sensing observations of fire and smoke plumes under day and night conditions. The emissions were linked to fuels consumed and fire radiative power using orbital and suborbital remote sensing observations collected during overflights of the fires and smoke plumes and ground sampling of fuels.

 

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.

 

We report on the sensitivity of enhanced ozone (O3) production, observed during lake breeze circulation along the coastline of Lake Michigan, to the concentrations of nitrogen oxides (NOx = NO + NO2) and volatile organic compounds (VOCs). We assess the sensitivity of O3 production to NOx and VOC on a high O3 day during the Lake Michigan Ozone Study 2017 (LMOS 2017) using an observationally-constrained chemical box model that implements the Master Chemical Mechanism (MCM v3.3.1) and recent emission inventories for NOx and VOCs. The MCM model is coupled to a backward air mass trajectory analysis from a ground supersite in Zion, IL where an extensive series of measurements of O3 precursors and their oxidation products, including hydrogen peroxide (H2O2), nitric acid (HNO3), and particulate nitrates (NO3-) serve as model constraints. We evaluate the chemical evolution of the Chicago-Gary urban plume as it advects over Lake Michigan and demonstrate how modeled indicators of VOC- vs. NOx- sensitive regimes can be constrained by measurements at the trajectory endpoint. Using the modeled ratio of the instantaneous H2O2 and HNO3 production rates (PH2O2 / PHNO3), we suggest that O3 production over the urban source region is strongly VOC-sensitive and progresses towards a more NOx-sensitive regime as the plume advects north along the Lake Michigan coastline on this day. We also demonstrate that ground-based measurements of the mean concentration ratio of H2O2 to HNO3 describe the sensitivity of O3 production to VOC and NOx as the integral of chemical production along the plume path.