CRC Report No. A-34 - Coordinating Research Council
CRC Report No. A-34 - Coordinating Research Council
CRC Report No. A-34 - Coordinating Research Council
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April 2005<br />
species (CNG and LPG for ethane and propane) that provided a way to account for the mass of<br />
these species. As discussed above, the names (CNG/aged and LPG) attached to these profiles<br />
needed careful interpretation because they describe chemical appearances rather than emission<br />
inventory source categories.<br />
Analyses of the grid model experiments revealed the extent to which source contributions were<br />
degraded by chemical reaction. The extent of chemical degradation varied with source profile<br />
and receptor location: high reactivity categories (e.g., biogenics) were depleted by up to 90%<br />
whereas low reactivity categories (e.g., CNG, LPG) were depleted ~10% by chemical reaction.<br />
As expected, the extent of chemical degradation was greater at downwind receptors.<br />
The experimental findings reviewed above show that CMB generally was able to correctly<br />
apportion the sum of PAMS species present in the air samples even when source profiles had<br />
been altered by chemically aging. Chemical reaction also changes the relative amounts of low<br />
and high reactivity source categories. For example, high reactivity biogenic emissions were<br />
degraded much more than low reactivity CNG or LPG emissions. The impact of chemical aging<br />
on source contributions must be considered when comparing source apportionment results to<br />
emission inventories. The experimental findings were that: Source apportionment results for<br />
highly reactive emissions categories (e.g., biogenic emissions) significantly under-estimate the<br />
actual contribution due to chemical degradation (finding 23). Source apportionment results for<br />
low reactivity categories (e.g. those labeled CNG or LPG) may over-estimate the real<br />
contributions of these categories due to chemical degradation (finding 24). Apart from biases for<br />
high and low reactivity categories, source apportionment results for other categories are not<br />
greatly influenced by chemical degradation except at far downwind receptors (finding 25).<br />
Spatial Heterogeneity in Emissions Sources<br />
CMB source contributions are often compared to emission inventories with the goal of<br />
evaluating and improving the emissions inventory. Air samples at a receptor location may be<br />
dissimilar from the local emissions because of spatial heterogeneity in the distribution of<br />
emissions sources. Comparisons of the known source contributions in air samples to local<br />
emissions showed that the impacts of spatial heterogeneity were most pronounced for downwind<br />
receptors and receptors located near major point sources (findings 23 and 24). The impacts of<br />
spatial heterogeneity in emissions inventories were least, but not absent, for urban/suburban<br />
receptors with a mix of residential/commercial/industrial emissions.<br />
Effects of spatial heterogeneity in emissions are likely under represented in the grid model<br />
experiments of this study compared to the real-world because (1) the grid model cannot represent<br />
micro-scale (sub 5-km) variations in emissions, and (2) grid modelers have limited information<br />
to spatially allocate emissions and so use spatial surrogates to allocate emissions (e.g.,<br />
population) which simplify the texture in the emissions inventory. Micro-scale impacts present a<br />
challenge to selecting regionally representative monitoring locations in a real-world study where<br />
the goal is to characterize a regional emissions inventory.<br />
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