The ratio of the concentration of the oxidation product anthraquinone to th
at of its parent polycyclic aromatic hydrocarbon anthracene is reported for
several coastal marine sediments. The ratio ranges from 0.317 in a highly
contaminated industrialized harbor to 2.81 in a remote, less contaminated s
ite. We hypothesize that differences in this ratio result from the input so
urce of PAHs, with input from atmospheric deposition at remote sites result
ing in a predominance of anthraquinone (ratio > 1), and direct discharge to
highly contaminated industrialized harbors resulting in a predominance of
anthracene (ratio < 1). To support this hypothesis, the fate of anthracene
in the marine environment was investigated with respect to conversion to it
s oxidation product, anthraquinone. Once associated with sediments, anthrac
ene is believed to be relatively persistent; however, it can potentially be
subjected to oxidation via biological (microbial degradation) and chemical
(chemical oxidation and photooxidation) processes. An assessment of the ex
tent of oxidation of anthracene associated with sediments was conducted bot
h under conditions simulating those found in the marine environment and und
er rigorous conditions by exposure to UV radiation. Results of this study s
how that while anthracene associated with marine sediments does not readily
undergo oxidation to anthraquinone under conditions normally encountered i
n the marine environment, under extreme conditions anthracene is photooxidi
zed by exposure to UV radiation. The extent of oxidation is influenced by s
ediment characteristics such as percent organic carbon, humic acid content
and sediment surface area. The relative stability of anthracene under norma
l conditions may help to validate the use of the anthraquinone to anthracen
e ratio in marine sediments as an environmental marker of contaminant sourc
e. (C) 1999 Elsevier Science Ltd. All rights reserved.