Carbon dioxide emissions to the atmosphere from inland waters-streams, rivers, lakes and reservoirs-are nearly equivalent to ocean and land sinks globally. Inland waters can be an important source of methane and nitrous oxide emissions as well, but emissions are poorly quantified, especially in Africa. Here we report dissolved carbon dioxide, methane and nitrous oxide concentrations from 12 rivers in sub-Saharan Africa, including seasonally resolved sampling at 39 sites, acquired between 2006 and 2014. Fluxes were calculated from published gas transfer velocities, and upscaled to the area of all sub-Saharan African rivers using available spatial data sets. Carbon dioxide-equivalent emissions from river channels alone were about 0.4 Pg carbon per year, equivalent to two-thirds of the overall net carbon land sink previously reported for Africa. Including emissions from wetlands of the Congo river increases the total carbon dioxide-equivalent greenhouse-gas emissions to about 0.9 Pg carbon per year, equivalent to about one quarter of the global ocean and terrestrial combined carbon sink. Riverine carbon dioxide and methane emissions increase with wetland extent and upland biomass. We therefore suggest that future changes in wetland and upland cover could strongly a ect greenhouse-gas emissions from African inland waters.C limate predictions necessitate a full and robust account of natural and anthropogenic greenhouse-gas (GHG) fluxes, especially for CO 2 (refs 1-3), CH 4 (ref. 4) and N 2 O (ref. 5), which together accounted for 94% of the anthropogenic global radiative forcing by well-mixed GHGs in 2011 relative to 1750 (ref. 6). Inland waters (streams, rivers, lakes and reservoirs) are increasingly recognized as important sources of GHGs to the atmosphere, with global CO 2 and CH 4 emissions estimated at 2.1 PgC yr −1 (ref.3) and 0.7 PgC yr −1 (CO 2 -equivalents; CO 2 e) (ref. 4) (1 Pg = 10 15 g), respectively. Considering that the oceanic and land carbon (C) sinks correspond to ∼1.5 and ∼2.0 PgC yr −1 (ref. 7), respectively, the GHG flux from inland waters is significant in the global C budget.In a recent global compilation of inland CO 2 data 3 , <20 data points (out of 6,708, that is, <0.3%) represented African inland waters (with the exception of South Africa, which has been densely sampled), even though they account for ∼12% of both global freshwater discharge 8 and riverine surface area 3 , and include some of the largest rivers and lakes in the world. Equally for the global CH 4 database, there is a strong under-representation of tropical inland waters, whereby a recent synthesis 4 resorted to extrapolating CH 4 fluxes from temperate rivers.The prevailing large uncertainty involved in GHG flux estimates for inland waters, essentially due to the paucity of available data, is coupled to a poor understanding of underlying processes, both of which preclude gauging of future fluxes in response to human pressures. In particular, there is a need to further understand the link between inland water GHG fluxes and ...

The role played by river networks in regional and global carbon (C) budgets is receiving increasing attention. Despite the potential of radiocarbon measurements (Δ 14 C) 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 14 C content of different riverine C pools. Here we present new 14 C data on particulate and dissolved organic C (POC and DOC) from six river basins in tropical and subtropical Africa and compiled >1400 literature Δ 14 C 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 Δ 14 C signature of À203‰, corresponding to an age of~1800 years B.P. For DOC exported to the coastal zone, we predict a modern (decadal) age (Δ 14 C = +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 14 C ages of dissolved inorganic carbon, but the available data favor the hypothesis that in most cases, more recent organic C is preferentially mineralized.

Abstract. Inland waters have been recognized as a significant source of carbon dioxide (CO 2 ) to the atmosphere at the global scale. Fluxes of CO 2 between aquatic systems and the atmosphere are calculated from the gas transfer velocity and the water-air gradient of the partial pressure of CO 2 (pCO 2 ). Currently, direct measurements of water pCO 2 remain scarce in freshwaters, and most published pCO 2 data are calculated from temperature, pH and total alkalinity (TA). Here, we compare calculated (pH and TA) and measured (equilibrator and headspace) water pCO 2 in a large array of temperate and tropical freshwaters. The 761 data points cover a wide range of values for TA (0 to 14 200 µmol L −1 ), pH (3.94 to 9.17), measured pCO 2 (36 to 23 000 ppmv), and dissolved organic carbon (DOC) (29 to 3970 µmol L −1 ). Calculated pCO 2 were > 10 % higher than measured pCO 2 in 60 % of the samples (with a median overestimation of calculated pCO 2 compared to measured pCO 2 of 2560 ppmv) and were > 100 % higher in the 25 % most organic-rich and acidic samples (with a median overestimation of 9080 ppmv). We suggest these large overestimations of calculated pCO 2 with respect to measured pCO 2 are due to the combination of two cumulative effects: (1) a more significant contribution of organic acids anions to TA in waters with low carbonate alkalinity and high DOC concentrations; (2) a lower buffering capacity of the carbonate system at low pH, which increases the sensitivity of calculated pCO 2 to TA in acidic and organicrich waters. No empirical relationship could be derived from our data set in order to correct calculated pCO 2 for this bias.Owing to the widespread distribution of acidic, organic-rich freshwaters, we conclude that regional and global estimates of CO 2 outgassing from freshwaters based on pH and TA data only are most likely overestimated, although the magnitude of the overestimation needs further quantitative analysis. Direct measurements of pCO 2 are recommended in inland waters in general, and in particular in acidic, poorly buffered freshwaters.

[1] Here we examine the patterns in carbon dioxide partial pressure (pCO 2 ) measured in a number of small boreal streams (<5 km in length) in the northwestern boreal region of Québec during the ice-free season and compare these to the patterns found in a major river (Eastmain River) and in a tributary in the same region. All systems were consistently supersaturated in CO 2 (range 450 to 5000 matm) streams having both higher (mean 1850 matm) and more variable pCO 2 than that of rivers (range 550 to 800 matm). Stream pCO 2 was positively related to DOC concentration and stream segment length, both suggesting a direct influence of the surrounding landscape. Calculated stream water-air CO 2 fluxes ranged from 700 to over 3000 mg C m À2 d À1 , up to 2 orders of magnitude higher than those measured in large rivers and lakes of the same region. Small streams, despite their extremely reduced areal coverage (1% of the aquatic surface), accounted for 25% of the total aquatic C emissions, and the resulting areal stream fluxes were comparable to those measured in different soils or wetlands in the region.

[1] Here we assess total sediment organic C stocks and long-term C accumulation rates in 13 boreal lakes in northern Québec spanning a wide range of morphometric shapes. The lake basins were mapped using a sub-bottom profiler to obtain total sediment volume, which we combined with organic carbon profiles from Holocene cores to obtain total C mass. The estimated long-term areal C accumulation rates averaged 3.8 g C m À2 yr À1 , lower than previous reports for other boreal and temperate regions. The difference relative to previous studies may have resulted from our use of the detailed echosounding mapping approach, which yields more realistic estimates of total sediment volume. Total sediment C stocks were not related to lake trophic status or to DOC concentration, but rather to lake area and to the lake dynamic ratio (√lake area/mean water depth). We hypothesize that scaling of C accumulation to lake morphometry is more a reflection of the intrinsic capacity of lakes to retain carbon. We show that C loading does in fact play a significant role in the patterns of C accumulation in lakes, but that this role is strongly modulated by both lake size and shape, which in turn determine the ability of lakes to retain the carbon that has been loaded. Upscaling to the regional level using the empirical lake size relationships developed here results in an areal-weighted average C stock of 23 kg C m À2 (per unit of lake area), or 3.8 kg m À2 (per unit landscape), which represents around 25% of the total landscape C storage in this boreal region. Because of the lake-size scaling of C accumulation, the total lake C stocks at the regional level depend not only on the total lake area, but more importantly on the local lake size distribution.Citation: Ferland, M.-E., P. A. del Giorgio, C. R. Teodoru, and Y. T. Prairie (2012), Long-term C accumulation and total C stocks in boreal lakes in northern Québec, Global Biogeochem. Cycles, 26, GB0E04,

Abstract. Spanning over 3000 km in length and with a catchment of approximately 1.4 million km2, the Zambezi River is the fourth largest river in Africa and the largest flowing into the Indian Ocean from the African continent. We present data on greenhouse gas (GHG: carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O)) concentrations and fluxes, as well as data that allow for characterization of sources and dynamics of carbon pools collected along the Zambezi River, reservoirs and several of its tributaries during 2012 and 2013 and over two climatic seasons (dry and wet) to constrain the interannual variability, seasonality and spatial heterogeneity along the aquatic continuum. All GHG concentrations showed high spatial variability (coefficient of variation: 1.01 for CO2, 2.65 for CH4 and 0.21 for N2O). Overall, there was no unidirectional pattern along the river stretch (i.e., decrease or increase towards the ocean), as the spatial heterogeneity of GHGs appeared to be determined mainly by the connectivity with floodplains and wetlands as well as the presence of man-made structures (reservoirs) and natural barriers (waterfalls, rapids). Highest CO2 and CH4 concentrations in the main channel were found downstream of extensive floodplains/wetlands. Undersaturated CO2 conditions, in contrast, were characteristic of the surface waters of the two large reservoirs along the Zambezi mainstem. N2O concentrations showed the opposite pattern, being lowest downstream of the floodplains and highest in reservoirs. Among tributaries, highest concentrations of both CO2 and CH4 were measured in the Shire River, whereas low values were characteristic of more turbid systems such as the Luangwa and Mazoe rivers. The interannual variability in the Zambezi River was relatively large for both CO2 and CH4, and significantly higher concentrations (up to 2-fold) were measured during wet seasons compared to the dry season. Interannual variability of N2O was less pronounced, but higher values were generally found during the dry season. Overall, both concentrations and fluxes of CO2 and CH4 were well below the median/average values for tropical rivers, streams and reservoirs reported previously in the literature and used for global extrapolations. A first-order mass balance suggests that carbon (C) transport to the ocean represents the major component (59%) of the budget (largely in the form of dissolved inorganic carbon, DIC), while 38% of the total C yield is annually emitted into the atmosphere, mostly as CO2 (98%), and 3% is removed by sedimentation in reservoirs.

[1] We present here the first comprehensive assessment of the carbon (C) footprint associated with the creation of a boreal hydroelectric reservoir (Eastmain-1 in northern Québec, Canada). This is the result of a large-scale, interdisciplinary study that spanned over a 7-years period (2003)(2004)(2005)(2006)(2007)(2008)(2009)), where we quantified the major C gas (CO 2 and CH 4 ) sources and sinks of the terrestrial and aquatic components of the pre-flood landscape, and also for the reservoir following the impoundment in 2006. The pre-flood landscape was roughly neutral in terms of C, and the balance between pre-and post-flood C sources/sinks indicates that the reservoir was initially (first year post-flood in 2006) a large net source of CO 2 (2270 mg C m À2 d À1) but a much smaller source of CH 4 (0.2 mg C m À2 d À1). While net CO 2 emissions declined steeply in subsequent years (down to 835 mg C m À2 d À1 in 2009), net CH 4 emissions remained constant or increased slightly relative to pre-flood emissions. Our results also suggest that the reservoir will continue to emit carbon gas over the long-term at rates exceeding the carbon footprint of the pre-flood landscape, although the sources of C supporting these emissions have yet to be determined. Extrapolation of these empirical trends over the projected life span (100 years) of the reservoir yields integrated long-term net C emissions per energy generation well below the range of the natural-gas combined-cycle, which is considered the current industry standard.

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.