Mechanisms of photochemical release of dissolved organic matter and iron from resuspended sediments
Xun Wang , Bin Hu , Peifang Wang , Tianli Bao , Jin Qian
DOI:10.1016/j.jes.2020.12.002
Received September 29, 2020,Revised , Accepted December 01, 2020, Available online December 24, 2020
Volume 33,2021,Pages 288-295
Photochemical reactions can alter the transformation of sedimentary organic matter into dissolved organic matter (DOM) and affect its ultimate fate in water ecosystems. In the present study, the photorelease of DOM and Fe from resuspended lake sediments was investigated under different O2 and NO3− concentration conditions to study the mechanisms of DOM and Fe photorelease. The amount of photoreleased Fe, which ranged from 0.22 to 0.70 μmol/L, was significantly linearly correlated with the amount of photoreleased DOM. O2 and NO3− could promote the photochemical release of DOM and Fe, especially during the initial 4 h irradiation. In general, the order of the photorelease rates of DOM and Fe under different conditions was as follows: NO3−/aerobic > aerobic ≈ NO3−/anaerobic > anaerobic. The photorelease rates of DOM and Fe were higher for the initial 4 hr irradiation than these for the subsequent 8 hr irradiation. The photorelease of DOM and Fe is thought to proceed via direct photodissolution and indirect processes. The relative contributions of indirect processes (>60%) was much greater than that of direct photodissolution (<40%). The photoproduced H2O2 under aerobic and anaerobic conditions indicated that hydroxyl radicals (•OH) are involved in the photorelease of DOM. Using •OH scavengers, it was found that 38.7%, 53.7%, and 77.6% of photoreleased DOM was attributed to •OH under anaerobic, aerobic, and NO3−/aerobic conditions, respectively. Our findings provide insights for understanding the mechanisms and the important role of •OH in the DOM and Fe photorelease from resuspended sediments.
