Among the nitrated and oxygenated polycyclic aromatic hydrocarbons (NPAHs and OPAHs) are some of the most hazardous substances to public health, mainly because of their carcinogenicity and oxidative potential. Despite these concerns, the concentrations and fate of NPAHs and OPAHs in the atmospheric environment are largely unknown. Ambient air concentrations of 18 NPAHs, 5 quinones, and 5 other OPAHs were determined at two urban and one regional background sites in central Europe. At one of the urban sites, the total (gas and particulate) concentrations of Σ10OPAHs were 10.0 ± 9.2 ng/m3 in winter and 3.5 ± 1.6 ng/m3 in summer. The gradient to the regional background site exceeded 1 order of magnitude. Σ18NPAH concentrations were typically 1 order of magnitude lower than OPAHs. Among OPAHs, 9-fluorenone and (9,10)-anthraquinone were the most abundant species, accompanied by benzanthrone in winter. (9,10)-Anthraquinone represented two-thirds of quinones. We found that a large fraction of the target substance particulate mass was carried by submicrometer particles. The derived inhalation bioaccessibility in the PM10 size fraction is found to be ≈5% of the total ambient concentration of OPAHs and up to ≈2% for NPAHs. For 9-fluorenone and (9,10)-anthraquinone, up to 86 and 18%, respectively, were found at the rural site. Our results indicate that water solubility could function as a limiting factor for bioaccessibility of inhaled particulate NPAHs and OPAHs, without considerable effect of surfactant lipids and proteins in the lung lining fluid.

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Surface water and atmospheric samples were collected across the tropical Atlantic Ocean on a transect of the R/V Endeavor in summer 2009 and analyzed for polycyclic aromatic hydrocarbons (PAHs). Across the entire tropical Atlantic Ocean, phenanthrene displayed on average highest dissolved concentrations (170 pg L(-1)), followed by pyrene (70 pg L(-1)) and fluoranthene (30 pg L(-1)). The Amazon plume was characterized by elevated dissolved concentrations of phenanthrene and benzo(g,h,i)fluoranthene. The warm eddy that we accidentally sampled at 66° W displayed highest concentrations of PAHs across the entire cruise, with phenanthrene, pyrene, and fluoranthrene all >1 ng L(-1). After having crossed the warm core, concentrations decreased back to previous levels. Samples taken in the Gulf Stream were below detection limit for all parent PAHs, implying very efficient removal processes. Dissolved dimethylphenanthrenes were frequently detected in the samples from the southern hemisphere, the Amazon plume, and in samples characteristic of the Gulf Stream and the U.S. East Coast. Atmospheric concentrations were dominated by gas-phase fluoranthene, pyrene, phenanthrene, and retene. Air-water gradients indicated that PAHs are mostly undergoing net deposition across the tropical Atlantic Ocean, with conditions closer to equilibrium off the U.S. East Coast and in Rhode Island Sound.