Fluorescence Spectroscopy Reveals Ubiquitous Presence of Oxidized and Reduced Quinones in Dissolved Organic Matter

荧光 氧化还原 化学 光化学 部分 荧光光谱法 环境化学 溶解有机碳 反应性(心理学) 光谱学 有机化学 病理 替代医学 物理 量子力学 医学
作者
Rose M. Cory,Diane M. McKnight
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:39 (21): 8142-8149 被引量:1710
标识
DOI:10.1021/es0506962
摘要

Excitation-emission matrixes (EEMs) of 379 dissolved organic matter (DOM) samples from diverse aquatic environments were modeled by parallel factor analysis (PARAFAC). Thirteen components likely representing groups of similarly fluorescing moieties were found to explain the variation in this data set. Seven of the thirteen components were identified as quinone-like based on comparison of their excitation and emission spectra to spectra of model quinones. These quinone-like fluorophores were found to vary in redox state and degree of conjugation. Two components were identified as amino acid-like based on comparison to tyrosine and tryptophan fluorescence spectra. The other four components are not yet associated with any class of molecules. The quinone-like fluorophores account for about 50% of the fluorescence for every sample analyzed, showing that quinone-like fluorophores are an important and ubiquitous fluorescing moiety and in natural waters. Further, the distribution of the quinone-like fluorophores was evaluated as a function of environmental and laboratory redox gradients. Under reducing conditions, the contribution of the reduced quinone-like fluorophores increased concurrentwith a decrease in the oxidized quinone-like fluorophores, indicating that DOM fluorescence is a function of redox state of quinone-like moieties. Lastly, a ratio of two quinone-like fluorophores was found to explain the variation in the fluorescence index. These results provide new insight into the redox reactivity of DOM and have implications for the application of fluorescence spectroscopy as a tool to characterize DOM.
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