Abstract

Sub-basins within the New York/New Jersey (NY/NJ) Harbor host variable amounts and sources of polycyclic aromatic hydrocarbons (PAHs). Analyses of radionuclides 137Cs and 7Be were used to assign approximate dates to individual sections of sediment cores collected from four major sub-basins of the harbor complex. Sampling sites range from heavily contaminated Newark Bay and Passaic River to less contaminated Raritan Bay and Jamaica Bay. PAHs were identified with GC–MS and quantified by GC respectively. Gas chromatography–isotope ratio mass spectrometry (GC/IRMS) was applied to determine δ 13C values of pyrene ( δ 13C Py), a principal 4 ring parent PAH. Two end-member PAH source components, petroleum-related PAHs (PRPAH) and combustion-related PAHs (CRPAH), were calculated from a carbon isotopic mass balance equation based on assumptions that petroleum-related δ 13C Py is −29‰, and that combustion-derived δ 13C Py is −24‰. Temporal trends of PRPAH in these cores are similar to those of the petroleum-derived unresolved complex mixture (UCM), whereas CRPAH resembled trends of “Total” PAH (TPAH). Three molecular ratios, fluoranthene to fluoranthene plus pyrene (Fl/(Fl + Py)), high molecular weight 4–6 ring PAH to total PAH (Ring456/TPAH) and parent to total (Par/(Par + Alkyl)), correlate strongly with each other, and show a moderate to strong positive correlation with δ 13C Py. In contrast, the ratios of anthracene to phenanthrene plus anthracene (A/(Pa + A)), benzo[ a]anthracene to benzo[ a]anthracene plus chrysene (BaA/(BaA+Chy)), and indeno[1,2,3- cd]pyrene to indeno[1,2,3- cd]pyrene plus benzo[ ghi]perylene (IP/(IP + Bghi)) show no, weak, or even negative correlation with the four well correlated ratios ( δ 13C Py, Par/(Par + Alkyl), Fl/(Fl + Py), and Ring456/TPAH). Combined application of the four well correlated molecular indicators suggests that PAH contribution from combustion became more important in most areas of the NY/NJ Harbor during the last three decades of the 20th century.

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