AI Article Synopsis

  • The study examined the antioxidant capacity and the formation of reactive intermediates (RIs) in water samples from the Florida Everglades, focusing on differences between marsh and estuarine environments as well as wet and dry seasons.
  • Multiple linear regression models provided better predictions of RIs and their quantum yields compared to single linear regression models, though they struggled with previous datasets due to intercorrelated predictors.
  • Findings indicated that hydroxyl radical (OH) formation is generally separate from the production of triplet excited states of dissolved organic matter (DOM*) and singlet oxygen (O), and also showed a negative correlation between the quantum yields of O and DOM* and antioxidant activity in the samples.

Article Abstract

The antioxidant capacity and formation of photochemically produced reactive intermediates (RI) was studied for water samples collected from the Florida Everglades with different spatial (marsh versus estuarine) and temporal (wet versus dry season) characteristics. Measured RI included triplet excited states of dissolved organic matter (DOM*), singlet oxygen (O), and the hydroxyl radical (OH). Single and multiple linear regression modeling were performed using a broad range of extrinsic (to predict RI formation rates, R) and intrinsic (to predict RI quantum yields, Φ) parameters. Multiple linear regression models consistently led to better predictions of R and Φ for our data set but poor prediction of Φ for a previously published data set,1 probably because the predictors are intercorrelated (Pearson's r > 0.5). Single linear regression models were built with data compiled from previously published studies (n ≈ 120) in which E2:E3, S, and Φ values were measured, which revealed a high degree of similarity between RI-optical property relationships across DOM samples of diverse sources. This study reveals that OH formation is, in general, decoupled from DOM* and O formation, providing supporting evidence that DOM* is not a OH precursor. Finally, Φ for O and DOM* correlated negatively with antioxidant activity (a surrogate for electron donating capacity) for the collected samples, which is consistent with intramolecular oxidation of DOM moieties by DOM*.

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http://dx.doi.org/10.1021/acs.est.6b06372DOI Listing

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