2008 Joint Annual Meeting (5-9 Oct. 2008): Effect of Different Electron Acceptors on Organic Carbon Mineralization and Transformation in a Freshwater Marsh.

775-4 Effect of Different Electron Acceptors on Organic Carbon Mineralization and Transformation in a Freshwater Marsh.



Wednesday, 8 October 2008
George R. Brown Convention Center, Exhibit Hall E
Syam Dodla, School of Plant Environmental and Soil Sciences, Louisiana State University, Tower Drive, 104 Madison B Sturgis Hall, Baton Rouge, LA 70803, Jim Wang, School of Plant Environmental and Soil Sciences, Louisiana State University, Tower Drive, 313 M.B. Sturgis Hall, Baton Rouge, LA 70803 and Ron DeLaune, Wetland Biogeochemistry Institute, Louisiana State University, 3239 Energy, Coast & Environment Bld, Dept. of Oceanography & Coastal Sciences, Baton Rouge, LA 70803
Carbon mineralization in wetlands is limited due to the low availability of oxygen. Under such anoxic conditions, the presence of alternative electron acceptors such as NO3-, and SO42- play a major role in the mineralization and transformation of organic carbon. Estimation of CH4 and CO2 production under different conditions is important for determining whether the wetlands serve as net C sinks or sources of atmospheric C. Kinetics of carbon gas emissions from a freshwater marsh soil treated with different levels of SO42- and NO3- under anoxic conditions were monitored for 101 days. The total amount of CO2 released did not show any significant difference among the treatments. However, the treatment effect was significant on CH4 emission. The amount of total CH4 released was the highest in the control sample followed by 2 mM SO4 2- > 5 mM SO4 2- > 3.2 mM NO3- > 5 mM NO3-. Methane production was decreased by more than 99 % at both 3.2 and 5 mM NO3- concentrations while 5 mM and 2 mM SO42- decreased 90 and 78 % respectively as compared to the control. Though there were no differences found in C mineralization rate, NO3- was showed to be the preferred electron acceptor than sulfate. Even though NO3- effectively decreased the CH4 emissions appreciable amount of N2O also released during the C mineralization. Overall results suggest that at equivalent concentrations between NO3- and SO42- CO2 emissions were similar.