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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 />

H:\crca<strong>34</strong>-receptor\report\Final\sec5.doc 5-8

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