Abstract. Measurements of aerosol composition, volatile organic compounds, and CO are used to determine biogenic secondary organic aerosol (SOA) concentrations at a rural site 70 km north of Toronto. These biogenic SOA levels are many times higher than past observations and occur during a period of increasing temperatures and outflow from Northern Ontario and Quebec forests in early summer. A regional chemical transport model approximately predicts the event timing and accurately predicts the aerosol loading, identifying the precursors as monoterpene emissions from the coniferous forest. The agreement between the measured and modeled biogenic aerosol concentrations contrasts with model underpredictions for polluted regions. Correlations of the oxygenated organic aerosol mass with tracers such as CO support a secondary aerosol source and distinguish biogenic, pollution, and biomass burning periods during the field campaign. Using the Master Chemical Mechanism, it is shown that the levels of CO observed during the biogenic event are consistent with a photochemical source arising from monoterpene oxidation. The biogenic aerosol mass correlates with satellite measurements of regional aerosol optical depth, indicating that the event extends across the eastern Canadian forest. This regional event correlates with increased temperatures, indicating that temperature-dependent forest emissions can significantly affect climate through enhanced direct optical scattering and higher cloud condensation nuclei numbers.

Meteorological observations from the BAQS-Met field experiment during the summer months of 2007 were integrated and manually analyzed in order to identify and characterize lake breezes in the southern Great Lakes region of North America, and assess their potential impact on air quality. Lake breezes occurred frequently, with one or more lake breezes identified on 90 % of study days. They affected all parts of the study region, including southwestern Ontario and nearby portions of southeast Lower Michigan and northern Ohio, with lake-breeze fronts occasionally penetrating from 100 km to over 200 km inland. Occurrence rates and penetration distances were found to be higher than previously reported in the literature. This comprehensive depiction of observed lake breezes allows an improved understanding of their influence on the transport, dispersion, and production of pollutants in this region. <br><br> The observational analyses were compared with output from subsequent runs of a high-resolution numerical weather prediction model. The model accurately predicted lake breeze occurrence and type in a variety of synoptic wind regimes, but selected cases showed substantial differences in the detailed timing and location of lake-breeze fronts, and with the initiation of deep moist convection. Knowledge of such strengths and weaknesses aids in the interpretation of results from air quality models driven by this meteorological model

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Abstract.A three-level nested regional air pollution model has been used to study the processes leading to high ozone concentrations in the southern Great Lakes region of North America. The highest resolution simulations show that complex interactions between the lake-breeze circulation and the synoptic flow lead to significant enhancements in the photochemical production and transport of ozone at the local scale. Mass tracking of individual model processes show that Lakes Erie and St. Clair frequently act as photochemical ozone production regions, with average mid-day production rates of up to 3 ppbv per hour. Enhanced ozone levels are evident over these two lakes in 23-day-average surface ozone fields. Analysis of other model fields and aircraft measurements suggests that vertical circulation enhances ozone levels at altitudes up to 1500 m over Lake St. Clair, whereas subsidence enhances ozone over Lake Erie in a shallow layer only 250 m deep. Mass tracking of model transport shows that lake-breeze surface convergence zones combined with the synoptic flow can then carry ozone and its precursors hundreds of kilometers from these source areas, in narrow, elongated features. Comparison with surface mesonet ozone observations confirm the presence, magnitude, and timing of these features, which can create local ozone enhancements on the order of 30 ppbv above the regional ozone levels. Sensitivity analyses of model-predicted ozone and HO x concentrations show that most of the region is VOC-limited, and that the secondary oxidation pathways of aromatic hydrocarbons have a key role in setting the region's ozone and HO x levels.

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