Canadian wildfire smoke impacted air quality across the northern Mid-Atlantic (MA) of the United States during June 9-12, 2015. A multiday exceedance of the new 2015 70-ppb National Ambient Air Quality Standard (NAAQS) for ozone (O 3 ) followed, resulting in Maryland being incompliant with the Environmental Protection Agency's (EPA) revised 2015 O 3 NAAQS. Surface in situ, balloon-borne, and remote sensing observations monitored the impact of the wildfire smoke at Maryland air quality monitoring sites. At peak smoke concentrations in Maryland, wildfire-attributable volatile organic compounds (VOCs) more than doubled, while non-NOx oxides of nitrogen (NOz) tripled, suggesting long range transport of NOx within the smoke plume. Peak daily average PM 2.5 was 32.5 µg m −3 with large fractions coming from black carbon (BC) and organic carbon (OC), with a synonymous increase in carbon monoxide (CO) concentrations. Measurements indicate that smoke tracers at the surface were spatially and temporally correlated with maximum 8-hr O 3 concentrations in the MA, all which peaked on June 11. Despite initial smoke arrival late on June 9, 2015, O 3 production was inhibited due to ultraviolet (UV) light attenuation, lower temperatures, and nonoptimal surface layer composition. Comparison of Community Multiscale Air Quality (CMAQ) model surface O 3 forecasts to observations suggests 14 ppb additional O 3 due to smoke influences in northern Maryland. Despite polluted conditions, observations of a nocturnal low-level jet (NLLJ) and Chesapeake Bay Breeze (BB) were associated with decreases in O 3 in this case. While infrequent in the MA, wildfire smoke may be an increasing fractional contribution to high-O 3 days, particularly in light of increased wildfire frequency in a changing climate, lower regional emissions, and tighter air quality standards.Implications: The presented event demonstrates how a single wildfire event associated with an ozone exceedance of the NAAQS can prevent the Baltimore region from complying with lower ozone standards. This relatively new problem in Maryland is due to regional reductions in NOx emissions that led to record low numbers of ozone NAAQS violations in the last 3 years. This case demonstrates the need for adequate means to quantify and justify ozone impacts from wildfires, which can only be done through the use of observationally based models. The data presented may also improve future air quality forecast models.PAPER HISTORY

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Ozone from a stratospheric intrusion (SI) reached sea level in association with a thunderstorm gust front during the predawn hours of 16 April 2018. The event caused surface ozone concentration increases of 30 to more than 50 ppbv in a matter of minutes in a band from approximately Richmond, Virginia, to Philadelphia, Pennsylvania. Peak hourly ozone concentrations reached 74 ppbv in northeastern Maryland despite absent photochemistry and ongoing convective activity. An intense jet stream with velocities >80 kt (41 m s−1) less than 1 km above ground level was observed associated with a deepening cyclone. Modern-Era Retrospective Analysis for Research and Applications, version 2 (MERRA-2), showed a filament of ozone with concentrations greater than 90 ppbv extending downward from the stratosphere to the lower troposphere. This SI filament became collocated with an ongoing severe squall line, and stratospheric ozone was transported directly to sea level when entrained into the squall-line gust front. Weather radar and in situ observations confirmed surface ozone increased with the thunderstorm gust front, while a concurrent reduction in carbon monoxide confirmed air within the gust front had stratospheric origins. While rare, such coupling events are important to troposphere–stratosphere exchanges and in overall atmospheric chemistry and climate. This may be the first event of its type and magnitude documented.