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.

Carbon in thawing permafrost soils may have global impacts on climate change; however, the factors that control its processing and fate are poorly understood. The dominant fate of dissolved organic carbon (DOC) released from soils to inland waters is either complete oxidation to CO2 or partial oxidation and river export to oceans. Although both processes are most often attributed to bacterial respiration, we found that photochemical oxidation exceeds rates of respiration and accounts for 70 to 95% of total DOC processed in the water column of arctic lakes and rivers. At the basin scale, photochemical processing of DOC is about one-third of the total CO2 released from surface waters and is thus an important component of the arctic carbon budget.

[1] Source, transformation, and preservation mechanisms of dissolved organic matter (DOM) remain elemental questions in contemporary marine and aquatic sciences and represent a missing link in models of global elemental cycles. Although the chemical character of DOM is central to its fate in the global carbon cycle, DOM characterizations in long-term ecological research programs are rarely performed. We analyzed the variability in the quality of 134 DOM samples collected from 12 Long Term Ecological Research stations by quantification of organic carbon and nitrogen concentration in addition to analysis of UV-visible absorbance and fluorescence spectra. The fluorescence spectra were further characterized by parallel factor analysis. There was a large range in both concentration and quality of the DOM, with the dissolved organic carbon (DOC) concentration ranging from less than 1 mgC/L to over 30 mgC/L. The ranges of specific UV absorbance and fluorescence parameters suggested significant variations in DOM composition within a specific study area, on both spatial and temporal scales. There was no correlation between DOC concentration and any DOM quality parameter, illustrating that comparing across biomes, large variations in DOM quality are not necessarily associated with corresponding large ranges in DOC concentrations. The data presented here emphasize that optical properties of DOM can be highly variable and controlled by different physical (e.g., hydrology), chemical (e.g., photoreactivity/redox conditions), and biological (e.g., primary productivity) processes, and as such can have important ecological consequences. This study demonstrates that relatively simple DOM absorbance and/or fluorescence measurements can be incorporated into long-term ecological research and monitoring programs, resulting in advanced understanding of organic matter dynamics in aquatic ecosystems.