Temporal variability and spatial dynamics of CO2 and CH4 concentrations and fluxes in the Zambezi River system

Spanning over 2900 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. Yet, there is surprisingly little or no information on carbon (C) cycling in this large river system. As part of a broader study on the riverine biogeochemistry in the Zambezi River basin, we present here mainstream dissolved CO2 and CH4 data collected during 2012 and 2013 over two climatic seasons (dry and wet) to constrain the interannual variability, seasonality and spatial heterogeneity of partial pressure of CO2 (pCO2) and CH4 concentrations and fluxes along the aquatic continuum, in relation to physico-chemical parameters (temperature, conductivity, oxygen, and pH) and various carbon pools (dissolved and particulate, organic and inorganic carbon, total alkalinity, primary production, respiration and net aquatic metabolism). Both pCO2 and CH4 variability was high, ranging from minimal values of 150 ppm and 7 nM, respectively, mainly in the two large reservoirs (the Kariba and the Cabora Bassa characterized by high pH and oxygen and low DOC), up to maximum values of 12,500 ppm and 12,130 nM, CO2 and CH4, respectively, mostly below floodplains/wetlands (low pH and oxygen levels, high DOC and POC concentrations). The interannual variability was relatively large for both CO2 and CH4 (mean pCO2: 2350 ppm in 2013 vs. 3180 ppm in 2013; mean CH4: 600 nM in 2012 vs. 1000 nM in 2013) and significantly higher (up to two fold) during wet season compared to dry season closely linked to distinct seasonal hydrological characteristics. Overall, no clear pattern was observed along the longitudinal gradient as river CO2 and CH4 concentrations are largely influenced by the presence of floodplains/wetlands, anthropogenic reservoirs or natural barriers (waterfalls/ rapids). Following closely the concentration patterns, river CO2 and CH4 mean fluxes of 3440 mg C-CO2 m-2 d-1 and 50 mg C-CH4 m-2 d-1, respectively, were well within the range of literature data for tropical river systems, while the two reservoirs were a sink of atmospheric CO2 (-240 mg C-CO2 m-2 d-1) and a low CH4 source (4 mg C-CH4 m-2 d-1)

Summer CO2 evasion from streams and rivers in the Kolyma River basin, north-east Siberia

Inland water systems are generally supersaturated in carbon dioxide (CO2) and are increasingly recognized as playing an important role in the global carbon cycle. The Arctic may be particularly important in this respect, given the abundance of inland waters and carbon contained in Arctic soils; however, a lack of trace gas measurements from small streams in the Arctic currently limits this understanding.We investigated the spatial variability of CO2 evasion during the summer low-flow period from streams and rivers in the northern portion of the Kolyma River basin in north-eastern Siberia. To this end, partial pressure of carbon dioxide (pCO2) and gas exchange velocities (k) were measured at a diverse set of streams and rivers to calculate CO2 evasion fluxes. We combined these CO2 evasion estimates with satellite remote sensing and geographic information system techniques to calculate total areal CO2 emissions. Our results show that small streams are substantial sources of atmospheric CO2 owing to high pCO2 and k, despite being a small portion of total inland water surface area. In contrast, large rivers were generally near equilibrium with atmospheric CO2. Extrapolating our findings across the Panteleikha-Ambolikha sub-watersheds demonstrated that small streams play a major role in CO2 evasion, accounting for 86% of the total summer CO2 emissions from inland waters within these two sub-watersheds. Further expansion of these regional CO2 emission estimates across time and space will be critical to accurately quantify and understand the role of Arctic streams and rivers in the global carbon budget

Unexpected large evasion fluxes of carbon dioxide from turbulent streams draining the world’s mountains

Inland waters, including streams and rivers, are active components of the global carbon cycle. Despite the large areal extent of the world’s mountains, the role of mountain streams for global carbon fluxes remains elusive. Using recent insights from gas exchange in turbulent streams, we found that areal CO2 evasion fluxes from mountain streams equal or exceed those reported from tropical and boreal streams, typically regarded as hotspots of aquatic carbon fluxes. At the regional scale of the Swiss Alps, we present evidence that emitted CO2 derives from lithogenic and biogenic sources within the catchment and delivered by the groundwater to the streams. At a global scale, we estimate the CO2 evasion from mountain streams to 167 ± 1.5 Tg C yr−1, which is high given their relatively low areal contribution to the global stream and river networks. Our findings shed new light on mountain streams for global carbon fluxes

The regional and global significance of nitrogen removal in lakes and reservoirs

Author Posting. © The Author(s), 2008. This is the author's version of the work. It is posted here by permission of Springer for personal use, not for redistribution. The definitive version was published in Biogeochemistry 93 (2009): 143-157, doi:10.1007/s10533-008-9272-x.Human activities have greatly increased the transport of biologically available N through watersheds to potentially sensitive coastal ecosystems. Lentic water bodies (lakes and reservoirs) have the potential to act as important sinks for this reactive N as it is transported across the landscape because they offer ideal conditions for N burial in sediments or permanent loss via denitrification. However, the patterns and controls on lentic N removal have not been explored in great detail at large regional to global scales. In this paper we describe, evaluate, and apply a new, spatially explicit, annual-scale, global model of lentic N removal called NiRReLa (Nitrogen Retention in Reservoirs and Lakes). The NiRReLa model incorporates small lakes and reservoirs than have been included in previous global analyses, and also allows for separate treatment and analysis of reservoirs and natural lakes. Model runs for the mid-1990s indicate that lentic systems are indeed important sinks for N and are conservatively estimated to remove 19.7 Tg N yr-1 from watersheds globally. Small lakes (< 50 km2) were critical in the analysis, retaining almost half (9.3 Tg N yr-1) of the global total. In model runs, capacity of lakes and reservoirs to remove watershed N varied substantially (0-100%) both as a function of climate and the density of lentic systems. Although reservoirs occupy just 6% of the global lentic surface area, we estimate they retain approximately 33% of the total N removed by lentic systems, due to a combination of higher drainage ratios (catchment surface area : lake or reservoir surface area), higher apparent settling velocities for N, and greater N loading rates in reservoirs than in lakes. Finally, a sensitivity analysis of NiRReLa suggests that, on-average, N removal within lentic systems will respond more strongly to changes in land use and N loading than to changes in climate at the global scale.The NSF26 Research Coordination Network on denitrification for support for collaboration (award number DEB0443439 to S.P. Seitzinger and E.A. Davidson). This project was also supported by grants to J.A. Harrison from California Sea Grant (award number RSF8) and from the U.S. Geological Survey 104b program and R. Maranger (FQRNT Strategic Professor)

Effects of agricultural land use on fluvial carbon dioxide, methane and nitrous oxide concentrations in a large European river, the Meuse (Belgium)

peer reviewedWe report a data-set of CO2, CH4, and N2O concentrations in the surface waters of the Meuse river network in Belgium, obtained during four surveys covering 50 stations (summer 2013 and late winter 2013, 2014 and 2015), from yearly cycles in four rivers of variable size and catchment land cover, and from 111 groundwater samples. Surface waters of the Meuse river network were over-saturated in CO2, CH4, N2O with respect to atmospheric equilibrium, acting as sources of these greenhouse gases to the atmosphere, although the dissolved gases also showed marked seasonal and spatial variations. Seasonal variations were related to changes in freshwater discharge following the hydrological cycle, with highest concentrations of CO2, CH4, N2O during low water owing to a longer water residence time and lower currents (i.e. lower gas transfer velocities), both contributing to the accumulation of gases in the water column, combined with higher temperatures favourable to microbial processes. Inter-annual differences of discharge also led to differences in CH4 and N2O that were higher in years with prolonged low water periods. Spatial variations were mostly due to differences in land cover over the catchments, with systems dominated by agriculture (croplands and pastures) having higher CO2, CH4, N2O levels than forested systems. This seemed to be related to higher levels of dissolved and particulate organic matter, as well as dissolved inorganic nitrogen in agriculture dominated systems compared to forested ones. Groundwater had very low CH4 concentrations in the shallow and unconfined aquifers (mostly fractured limestones) of the Meuse basin, hence, should not contribute significantly to the high CH4 levels in surface riverine waters. Owing to high dissolved concentrations, groundwater could potentially transfer important quantities of CO2 and N2O to surface waters of the Meuse basin, although this hypothesis remains to be tested

Hysteresis effects in organic matter turnover in a tropical floodplain during a flood cycle

Tropical inland waters are increasingly recognized for their role in the global carbon cycle, but uncertainty about the effects of such systems on the transported organic matter remains. The seasonal interactions between river, floodplain, and vegetation result in highly dynamic systems, which can exhibit markedly different biogeochemical patterns throughout a flood cycle. In this study, we determined rates and governing processes of organic matter turnover. Multi-probes in the Barotse Plains, a pristine floodplain in the Upper Zambezi River (Zambia), provided a high-resolution data set over the course of a hydrological cycle. The concentrations of oxygen, carbon dioxide, dissolved organic carbon, and suspended particulate matter in the main channel showed clear hysteresis trends with expanding and receding water on the floodplain. Lower oxygen and suspended matter concentrations prevailed at longer travel times of water in the floodplain, while carbon dioxide and dissolved organic carbon concentrations were higher when the water spent more time on the floodplain. Maxima of particulate loads occurred before highest water levels, whereas the maximum in dissolved organic carbon load occurred during the transition of flooding and flood recession. Degradation of terrestrial organic matter occurred mainly on the floodplain at increased floodplain residence times. Our data suggest that floodplains become more intense hotspots at prolonged travel time of the flood pulse over the floodplain.ISSN:0168-2563ISSN:1573-515

Dynamics of greenhouse gases (CO2, CH4, N2O) along the Zambezi River and major tributaries, and their importance in the riverine carbon budget

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.AFRIVA