Atmospheric & Oceanic Science Research Works

Permanent URI for this collectionhttp://hdl.handle.net/1903/1596

Formerly known as the Department of Meteorology.

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Author: search.filters.author.Dickerson, Russell R.End date: 2009

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    Analysis of Summertime PM2.5 and haze in the Mid-Atlantic Region
    (Air & Waste Management Association (A&WMA), 2003) Chen, L.-W. Antony; Chow, Judith C.; Doddridge, Bruce G.; Dickerson, Russell R.; Ryan, William F.; Mueller, Peter K.
    Observations of the mass and chemical composition of particles less than 2.5 µm in aerodynamic diameter (PM2.5), light extinction, and meteorology in the urban Baltimore-Washington corridor during July 1999 and July 2000 are presented and analyzed to study summertime haze formation in the mid-Atlantic region. The mass fraction of ammoniated sulfate (SO4^2-) and carbonaceous material in PM2.5 were each ~50% for cleaner air (PM2.5 < 10 µg/m3) but changed to ~60% and ~20%, respectively, for more polluted air (PM2.5 > 30 µg/m3). This signifies the role of SO4^2- in haze formation. Comparisons of data from this study with the Interagency Monitoring of Protected Visual Environments network suggest that SO4^2- is more regional than carbonaceous material and originates in part from upwind source regions. The light extinction coefficient is well correlated to PM2.5 mass plus water associated with inorganic salt, leading to a mass extinction efficiency of 7.6 ± 1.7 m2/g for hydrated aerosol. The most serious haze episode occurring between July 15 and 19, 1999, was characterized by westerly transport and recirculation slowing removal of pollutants. At the peak of this episode, 1-hr PM2.5 concentration reached ~45 µg/m3, visual range dropped to ~5 km, and aerosol water likely contributed to ~40% of the light extinction coefficient.
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    The Sensitivity of Modeled Ozone to the Temporal Distribution of Point, Area, and Mobile Emissions in the Eastern US
    (Elsevier, 2009) Castellanos, Patricia; Ehrman, Sheryl H.; Stehr, Jeffrey W.; Dickerson, Russell R.
    Ozone remains one of the most recalcitrant air pollution problems in the US. Hourly emissions fields used in air quality models (AQMs) generally show less temporal variability than corresponding measurements. In order to understand how the daily cycle of estimated emissions affects modeled ozone, we analyzed the effects of altering all anthropogenic emissions’ temporal distributions by source group 2 on 2002 summer-long simulations of ozone using the Community Multi-Scale Air Quality Model (CMAQ) v4.5 and the carbon bond IV (CBIV) chemical mechanism with a 12 km grid. We find that when mobile source emissions were made constant over the course of a day, 8-hour maximum ozone predictions changed by ±7 parts per billion by volume (ppbv) in urban areas on days when ozone concentrations greater than 80 ppbv were simulated in the base case. Increasing the temporal variation of point sources resulted in ozone changes of +6 and –6 ppbv, but only for small areas near sources. Changing the daily cycle of mobile source emissions produces substantial changes in simulated ozone, especially in urban areas at night; implications for abatement strategy are discussed.