Cristian R. Teodoru

The age of river‐transported carbon: A global perspective

The role played by river networks in regional and global carbon (C) budgets is receiving increasing attention. Despite the potential of radiocarbon measurements (Δ14C) to elucidate sources and cycling of different riverine C pools, there remain large regions for which no data are available and no comprehensive attempts to synthesize the available information and examine global patterns in the 14C content of different riverine C pools. Here we present new 14C data on particulate and dissolved organic C (POC and DOC) from six river basins in tropical and subtropical Africa and compiled >1400 literature Δ14C data and ancillary parameters from rivers globally. Our analysis reveals a consistent pattern whereby POC is progressively older in systems carrying higher sediment loads, coinciding with a lower organic carbon content. At the global scale, this pattern leads to a proposed global median Δ14C signature of −203‰, corresponding to an age of ~1800 years B.P. For DOC exported to the coastal zone, we predict a modern (decadal) age (Δ14C = +22 to +46‰), and paired data sets confirm that riverine DOC is generally more recent in origin than POC—in contrast to the situation in ocean environments. Weathering regimes complicate the interpretation of 14C ages of dissolved inorganic carbon, but the available data favor the hypothesis that in most cases, more recent organic C is preferentially mineralized.

Divergent biophysical controls of aquatic CO2 and CH4 in the World’s two largest rivers

Carbon emissions to the atmosphere from inland waters are globally significant and mainly occur at tropical latitudes. However, processes controlling the intensity of CO2 and CH4 emissions from tropical inland waters remain poorly understood. Here, we report a data-set of concurrent measurements of the partial pressure of CO2 (pCO2) and dissolved CH4 concentrations in the Amazon (n = 136) and the Congo (n = 280) Rivers. The pCO2 values in the Amazon mainstem were significantly higher than in the Congo, contrasting with CH4 concentrations that were higher in the Congo than in the Amazon. Large-scale patterns in pCO2 across different lowland tropical basins can be apprehended with a relatively simple statistical model related to the extent of wetlands within the basin, showing that, in addition to non-flooded vegetation, wetlands also contribute to CO2 in river channels. On the other hand, dynamics of dissolved CH4 in river channels are less straightforward to predict, and are related to the way hydrology modulates the connectivity between wetlands and river channels.

Linking organic carbon sedimentation, burial efficiency, and long‐term accumulation in boreal lakes

Carbon (C) storage in lakes is now recognized as a significant sink of C at a global scale, but the pathways that lead to this storage remain poorly understood. In this study, we attempt to reconstruct and connect the processes that lead to long-term C accumulation in boreal lakes. These include the rate of particulate organic C (POC) sedimentation in the water column and sediment metabolism operating at a temporal scale of weeks to months, organic C accumulation in the top sediment layers integrated over scales of tens of years, and long-term organic C burial in lake sediment integrated over hundreds to thousands of years. The sinking POC flux was tenfold higher than the short-term sediment C accumulation rates in all systems, and we found no direct relationship between this downward C flux and either the short-term or long-term C accumulation rates. However, the resulting C burial efficiency (which ranged from 5 to 62%) was strongly related to lake shape, which ultimately constrains the time freshly deposited material that is exposed to oxygen and thereby regulates the fraction of the carbon sinking flux that is mineralized back to the atmosphere or permanently buried in the sediments. Small and deep lakes act as more efficient C sinks than large and flat lakes. We also show that long-term burial rates are nearly identical to current centennial-scale accumulation rates and that therefore, little degradation occurs after a few decades. Sediment C storage tends to be small (<5%) relative to lake C emissions, but that this balance is also strongly related to lake morphometry.

Contrasting biogeochemical characteristics of the Oubangui River and tributaries (Congo River basin)

The Oubangui is a major tributary of the Congo River. We describe the biogeochemistry of contrasting tributaries within its central catchment, with watershed vegetation ranging from wooded savannahs to humid rainforest. Compared to a 2-year monitoring record on the mainstem Oubangui, these tributaries show a wide range of biogeochemical signatures, from highly diluted blackwaters (low turbidity, pH, conductivity, and total alkalinity) in rainforests to those more typical for savannah systems. Spectral analyses of chromophoric dissolved organic matter showed wide temporal variations in the Oubangui compared to spatio-temporal variations in the tributaries, and confirm that different pools of dissolved organic carbon are mobilized during different hydrological stages. δ13C of dissolved inorganic carbon ranged between −28.1‰ and −5.8‰, and was strongly correlated to both partial pressure of CO2 and to the estimated contribution of carbonate weathering to total alkalinity, suggesting an important control of the weathering regime on CO2 fluxes. All tributaries were oversaturated in dissolved greenhouse gases (CH4, N2O, CO2), with highest levels in rivers draining rainforest. The high diversity observed underscores the importance of sampling that covers the variability in subcatchment characteristics, to improve our understanding of biogeochemical cycling in the Congo Basin.