4.6 Article

A multivariate approach to polycyclic aromatic hydrocarbon source apportionment in Connecticut, USA using compound-specific isotopic compositions

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ENVIRONMENTAL EARTH SCIENCES
卷 81, 期 6, 页码 -

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SPRINGER
DOI: 10.1007/s12665-022-10306-y

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Source apportionment; Polycyclic aromatic hydrocarbons (PAHs); Diagnostic ratios; Pollutant transport; Compound-specific isotopic composition

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  1. UConn College of Liberal Arts and Sciences

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Polycyclic aromatic hydrocarbons (PAHs) are environmental pollutants with mutagenic/carcinogenic properties. This study examines the spatial variations in PAH distributions and isotopic compositions among soils and sediments in Connecticut, USA. The results show that PAHs have relatively consistent distributions, primarily produced by pyrogenesis, with different sources for marine and fluvial samples.
Polycyclic aromatic hydrocarbons (PAHs) are environmental pollutants of concern due to their mutagenic/carcinogenic properties-identifying the source and transport of these compounds in the environment poses a significant challenge. Molecular distributions and stable isotopic compositions of PAHs vary as a function of both source and production/degradation processes, providing an opportunity to delineate origin and transport through the environment. This study utilizes a multivariate approach to examine spatial variations in PAH distributions and isotopic compositions (delta C-13 and delta D) among soils and sediments in Connecticut, USA. Data show that, despite large variations in industrial activity and land use history as well as total PAH abundance within sediment sample, the distribution of PAHs is relatively consistent across sites-on average, 9.2% 2-3 ring, 48.1% 4 ring, 33.7% 5 ring, and 9.0% 6 ring compounds. This distribution indicates a mixture of sources primarily produced by pyrogenesis. Marine samples plot in a unique dual diagnostic ratio space of the PAHs, indicating a different source of combustion materials for maritime industry. In addition, they exhibit significantly lower proportions of low molecular weight PAHs due to solubility effects and remobilization. Fluvial samples mimic terrestrial signals, suggesting predominant sources of airborne deposition and terrestrial runoff. Compound-specific delta C-13 and delta D are highly variable, ranging from -27.4 to -20.6 parts per thousand and -132 to -33 parts per thousand, respectively. Based on established endmember isotopic compositions, PAHs collected from Connecticut reflect a mixture of three main sources: liquid fossil fuel combustion, low temperature coal combustion, and high temperature industrial processes.

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