The photodegradation of domoic acid in model seawater containing varying amounts of total Fe(lll) (expressed as Fe(lll)), NO(3-), total phosphate (expressed as P04(3-)), and dissolved organic matter (DOM) is reported. A multivariate, microscale, high-throughput experimental approach is described for evaluating how these components interact to control the removal of domoic acid from natural waters. Under the nominal conditions of the study ([Fe(lll)]o 0-4 microM; [N03-]o 0-35 microM; [P04(3-)]o 0-4 microM; [DOM]o 0-10 mg/ L), it is apparent that Fe(lll) and DOM are significant promoters of domoic acid photooxidation. In contrast, P04(3-) interacts with Fe(lll) to inhibit the photooxidation of domoic acid, but P04(3-) alone does not act to slow or accelerate domoic acid photodegradation. No other variables (singly or interactively) have a statistically significant impact. At an incident light intensity of 765 W/m2 and initial domoic acid concentration of 0.96 microM, domoic acid half-lives range over 12-36 h, with half-life a function of [Fe(III)], [PO4(3-)], and dissolved organic matter loadings. An NMR based technique for measuring domoic acid-Fe(lll) binding (1.72 x 10(11)) is reported.
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Fisher et al. (2006) studied this question.
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