B023-04
Hotspots of diffusive CO2 and CH4 emission shift seasonally in four tropical reservoirs

Tuesday, 8 December 2020: 07:12
Virtual
Jose Paranaiba1, Nathan Barros2, Rafael Almeida3, Annika Linkhorst4, Raquel Mendonça2, Roseilson Souza do Vale5, Fábio Roland2 and Sebastian Sobek6, (1)Federal University of Juiz de Fora, Juiz de Fora, MNG, Brazil, (2)Federal University of Juiz de Fora, Juiz de Fora, Brazil, (3)Yachay Tech University, Department of Earth, Energy and Environmental Sciences, Imbabura, Ecuador, (4)Uppsala University, Uppsala, Sweden, (5)National Institute for Amazon Research (INPA), Manaus, AM, Brazil, (6)Uppsala University, Limnology, Department of Ecology and Genetics, Uppsala, Sweden
Abstract:
Reservoirs are globally significant sources of carbon dioxide (CO2) and methane (CH4) to the atmosphere. The patterns of spatial and temporal variability of CO2 and CH4 emission from reservoirs are still poorly studied, especially in tropical regions where hydropower is growing. We performed spatially resolved measurements of dissolved CO2 and CH4 surface water concentrations and their gas-exchange coefficients (k) to compute diffusive carbon flux from four contrasting tropical reservoirs across Brazil during different hydrological seasons. The diffusive emission of CO2 was higher during the dry season than during the rainy season, while there was no consistent seasonal patterns for the diffusive emission of CH4. Our results reveal that not only the magnitude, but also the spatial patterns of diffusive CO2 and CH4 flux varied strongly among hydrological seasons. River inflow areas were often characterized by high seasonality in diffusive flux. Additionally, spatial patterns of between-season variability were not consistent for CO2 and CH4: areas close to the dam generally showed low seasonal variability of diffusive CH4 flux but high variability of diffusive CO2 flux. Overall, we found that reservoir areas exhibiting highest emission rates (‘hotspots’) shifted substantially across seasons. Variance-based sensitivity analysis revealed that most of the variability in diffusive CO2 and CH4 flux was primarily driven by short-term variability in k, rather than by gas concentration changes in the surface water. Estimates of total diffusive carbon emission (CO2+CH4) from the reservoir surfaces differed by a factor of 2.7 (median; range: 1.1 – 13.0) between seasons, indicating that spatially-resolved measurements of gas concentrations and k need to be performed at different hydrological seasons in order to constrain annual diffusive carbon emission.