Short-term photodegradation of autochthonous and allochthonous dissolved organic matter in Lake Taihu, China.

Photochemistry is one of the key processes that shape the quality of dissolved organic matter (DOM) in aquatic systems, yet the photoreactivity of DOM from different sources remains largely unclear. In this study, DOM from 10 typical autochthonous and allochthonous sources in Lake Taihu basin were exposed to simulated sunlight, and quantitative and compositional changes of the DOM were explored by measuring its UV-Visable absorption and fluorescence spectroscopy. Photochemical release of nutrients was also explored during the incubations. Results showed that, although DOM from most sources experienced photobleaching effects with decreased absorption coefficients at 254 nm (a(254)) and fluorescence component intensities after light exposure, photochemical alterations of DOM linked to their original composition. Macrophyte-derived (Potamogeton malaianus) DOM, with the largest molecular size, showed increased a(254), humic- and protein-like fluorescence component (C1 and C2) abundances, and inorganic nutrient concentrations relative to dark controls, indicating photo-release of labile components. However, DOM with relatively higher aromaticity, e.g., from agricultural water and the lake, showed photobleaching effects and increased humification degree, probably due to the loss of aromatic components. Allochthonous anthropogenic DOM, e.g., from sewage, showed stronger photo-ammonification, likely relating to the fresh labile N-containing compositions. The form of inorganic nutrient releases during the DOM photolysis also varied with the original DOM sources. Macrophyte-derived DOM incubations showed larger photo-releases of NO3- and PO43-, while NO2- dominated inorganic nutrient releases during groundwater DOM light incubations. Thus, this study concludes that the photoreactivity of DOM closely relates to its original composition and sources.

Triolein embedded cellulose acetate membrane as a tool to evaluate sequestration of PAHs in lake sediment core at large temporal scale.

Although numerous studies have addressed sequestration of hydrophobic organic compounds (HOCs) in laboratory, little attention has been paid to its evaluation method in field at large temporal scale. A biomimetic tool, triolein embedded cellulose acetate membrane (TECAM), was therefore tested to evaluate sequestration of six PAHs with various hydrophobicity in a well-dated sediment core sampled from Nanyi Lake, China. Properties of sediment organic matter (OM) varying with aging time dominated the sequestration of PAHs in the sediment core. TECAM-sediment accumulation factors (MSAFs) of the PAHs declined with aging time, and significantly correlated with the corresponding biota-sediment accumulation factors (BSAFs) for gastropod (Bellamya aeruginosa) simultaneously incubated in the same sediment slices. Sequestration rates of the PAHs in the sediment core evaluated by TECAM were much lower than those obtained from laboratory study. The relationship between relative availability for TECAM (MSAF(t)/MSAF(0)) and aging time followed the first order exponential decay model. MSAF(t)/MSAF(0) was well-related to the minor changes of the properties of OM varying with aging time. Compared with chemical extraction, sequestration reflected by TECAM was much closer to that by B. aeruginosa. In contrast to B. aeruginosa, TECAM could avoid metabolism and the influences from feeding and other behaviors of organisms, and it is much easier to deploy and ready in laboratory. Hence TECAM provides an effective and convenient way to study sequestration of PAHs and probably other HOCs in field at large temporal scale.