Abstract
Particulate matter (PM) is associated with human health effects but the apparent toxicity of PM in epidemiological studies varies with season. PM toxicity may change due to seasonal shifts in composition or particle size distributions that in turn affect respiratory deposition efficiencies. In the current study, size-resolved PM composition was measured in the largest city (Fresno) in California's heavily polluted San Joaquin Valley during the summer (30 days) and winter (20 days) between 2006 and 2009 for 21 metals, organic carbon, elemental carbon, and 7 water-soluble ions. The Multiple-Path Particle Dosimetry model was applied to determine if seasonal variation in size-resolved composition influences respiratory deposition patterns. Mg, Al, S, V, Mn, Fe, Ni, Ba, SO4 2-, Na+, and Ca2+ had larger total deposition efficiencies (p < 0.004) during the summer versus the winter in all three regions of the respiratory tract. This trend results from increased relative concentrations of the target analytes per μg m−3 ambient PM1.8 concentration and would be detected with routine PM2.5 filter samples. V, Zn, Se, NO3 -, SO4 2-, and NH4 + also experienced seasonal size distribution shifts that enhanced the specific deposition efficiency in the tracheobronchial and pulmonary regions during the summer months (p < 0.05). This enhanced deposition would not be detected by routine filter samples because all of the size distribution changes occur at particle diameters <2.5 μm. This study demonstrates that changes to the particle size distributions (<2.5 μm) can enhance respiratory deposition efficiencies for trace metals and/or water-soluble ions and this may contribute to seasonal shifts in PM toxicity.
Published Version
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