Abstract. This paper describes the scientific and structural updates to the latest release of the Community Multiscale Air Quality (CMAQ) modeling system version 4.7 (v4.7) and points the reader to additional resources for further details. The model updates were evaluated relative to observations and results from previous model versions in a series of simulations conducted to incrementally assess the effect of each change. The focus of this paper is on five major scientific upgrades: (a) updates to the heterogeneous N 2 O 5 parameterization, (b) improvement in the treatment of secondary organic aerosol (SOA), (c) inclusion of dynamic mass transfer for coarse-mode aerosol, (d) revisions to the cloud model, and (e) new options for the calculation of photolysis rates. Incremental test simulations over the eastern United States during January and August 2006 are evaluated to assess the model response to each scientific improvement, providing explanations of differences in results between v4.7 and previously released CMAQ model versions. Particulate sulfate predictions are improved across all monitoring networks during both seasons due to cloud module updates. Numerous updates to the SOA module improve the simulation of seasonal variability and decrease the bias in organic carbon predictions at urban sites in the winter. Bias in the total mass of fine particulate matter (PM 2.5 ) is dominated by overpredictions of unspeciated PM 2.5 (PM other ) in the winter and by underpredictions of carbon in the summer. The CMAQv4.7 model results show slightly worse performance for ozone predictions.Correspondence to: K. M. Foley (foley.kristen@epa.gov) However, changes to the meteorological inputs are found to have a much greater impact on ozone predictions compared to changes to the CMAQ modules described here. Model updates had little effect on existing biases in wet deposition predictions.
Fine particulate matter emitted during wood combustion is known to contribute a significant fraction of the total fine aerosol concentration in the atmosphere of both urban and rural areas. In the present study, additional organic compounds that may act as wood smoke tracers in the atmosphere are sought. Polar organic compounds in wood smoke fine particulate matter are converted to their trimethylsilyl derivatives and analyzed by gas chromatography/mass spectrometry. Silylation enables the detection of n-alkanols, plant sterols, and a number of compounds derived from wood lignin that have not previously been reported in wood smoke samples, as well as levoglucosan and related sugar anhydrides formed during the combustion of cellulose. The concentrations of these compounds measured in source emissions are compared to the concentrations in atmospheric fine particle samples collected at a rural background site and at two urban sites in California's San Joaquin Valley. On the basis of this analysis, the sugar anhydrides galactosan and mannosan can be listed along with levoglucosan as being among the most abundant organic compounds detected in all samples.
With harmful ozone concentrations tied to meteorological conditions, EPA investigates the U.S. air quality implications of a changing climate. Consequently, the 03 NAAQS are most often exceeded during summertime hot spells in places with large natural or anthropogenic precursor emissions (e.g., cities and suburban areas). Table 2 The average maximum or minimum temperature and/or changes in their spatial distribution and duration, leading to a change in reaction rate coefficients and the solubility of gases in cloud water solution;The frequency and pattern of cloud cover, leading to a change in reaction rates and rates of conversion of S02to acid deposition;The frequency and intensity of stagnation episodes or a change in the mixing layer, leading to more or less mixing of polluted air with background air;Background boundary layer concentrations of water vapor, hydrocarbons, NOx, and 03, leading to more or less dilution of polluted air in the boundary layer and altering the chemical transformation rates;
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