Ozone concentrations in excess of health‐based standards occur along the coastline of Lake Michigan. A complex pattern of ozone precursor emissions interfaces with a complex meteorological environment, presenting a challenge for air quality management and simulation. Precursors are transported into a shallow, stable boundary layer over the lake. This is followed by ozone formation and transport back onshore through a combination of synoptic and lake breeze winds. In this study, we use measurements during the Lake Michigan Ozone Study 2017 (LMOS) to quantitatively evaluate the Weather Research and Forecasting with Chemistry (WRF‐Chem) model at 4 km horizontal resolution for key features of high ozone episodes over Southern Lake Michigan, with a focus on meteorological performance. WRF‐Chem showed good performance and successful reproduction of meteorological fields and clouds. Lake breeze model skill was inconsistent, with both good and poor performance depending on site and day. The combination of Noah land surface model and High‐Resolution Rapid Refresh meteorology gave the best performance with the mean bias of −0.5 °C for temperature, −0.6 °C for dewpoint temperature, and −0.3 m/s for wind speed along the western coast of Lake Michigan during the daytime. For ozone, WRF‐Chem was biased low (−4.4 ppb mean bias for daytime ozone) and underestimated hourly peak ozone. In some cases, ozone bias can be attributed to transport and lake breeze errors. Average ozone concentration showed minor (<2 ppb) sensitivity to changes to meteorology initial and boundary conditions or the land surface model.

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The Lake Michigan Ozone Study 2017 (LMOS 2017) was a collaborative multi-agency 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 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.

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 pre-existing 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.

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