Retention of Sediments and Nutrients in the Iron Gate I Reservoir on the Danube River

This work addresses an intensively debated question in biogeochemical research: "Are large dams affecting global nutrient cycles?” It has been postulated that the largest impoundments on the Lower Danube River, the Iron Gates Reservoirs, act as a major sink for silica (Si) in the form of settling diatoms, for phosphorus (P) and to a lesser extent for nitrogen (N). This retention of P and N in the reservoir would represent a positive contribution to the nutrient reduction in the Danube River. Based on a 9-month monitoring scheme in 2001, we quantified the nutrient and the sediment retention capacity of the Iron Gate I Reservoir. The sediment accumulation corresponded to 5% TN (total nitrogen), 12% TP (total phosphorus) and 55% TSS (total suspended solids) of the incoming loading. A mass balance revealed that more N and P are leaving the reservoir than entering via the inflow. Based on these current results, the reservoir was temporarily acting as a small nutrient source. The nutrient accumulation in the sediments of the Iron Gate I Reservoir represents only 1% of the "missing” load of 106t N and 1.3 × 105t P defined as the difference between the estimated nutrient export from the Danube Basin and the measured flux entering the Black Sea. This result disproves the hypothesis that the largest impoundment on the Danube River, the Iron Gates Reservoir, plays a major role in N and P eliminatio

Biogenic silica accumulation in the sediments of Iron Gate I Reservoir on the Danube River

Abstract.: Damming of rivers can result in severe downstream effects such as changing sediment and nutrient fluxes that potentially affect coastal ecosystems. Closing of the Iron Gates Dams in the lower Danube River was linked to a decrease in dissolved silica flux to the Black Sea of 600,000 t yr−1. A recent study on the Iron Gate I, however, indicated a dissolved silica removal within the reservoir of only 16,000 t yr−1. Such an order of magnitude difference between actual budgets and earlier estimates is unlikely to be caused by changes in hydrological or biogeochemical conditions. In order to separate annual variations and downstream effects of damming, we analyzed the sedimentary records of biogenic silica using dated sediments. Results confirm the detailed budgets of dissolved silica. In 2001, a total biogenic silica accumulation in the sediments of the Iron Gate I Reservoir of 19,000 t Si yr−1 was determined and represents the highest retention over the past 20 years. The accumulation of biogenic silica in the Iron Gate I Reservoir was compared with data from the coastal Black Sea. Biogenic silica in the sediments of the coastal Black Sea start decreasing before Iron Gate I Dam was completed in 1971. In conclusion, construction of the largest impoundment on the Danube River, the Iron Gate I Reservoir, was not solely responsible for decreasing the silica loads downstream at the coastal Black Se

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. d13C of dissolved inorganic carbon ranged between -28.1 per mil and -25.8 per mil, 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.AFRIVAL: ‘‘African river basins: catchment-scale carbon fluxes and transformations’

Retention of Sediments and Nutrients in the Iron Gate I Reservoir on the Danube River

ISSN:0168-2563ISSN:1573-515

Biogenic silica accumulation in the Iron Gates reservoir of the Danube River

ISSN:1015-1621ISSN:1420-905

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.AFRIVA

Spatio-temporal variations in lateral and atmospheric carbon fluxes from the Danube Delta

River deltas, with their mosaic of ponds, channels and seasonally inundated areas, act as the last continental hot spots of carbon turnover along the land–ocean aquatic continuum. There is increasing evidence for the important role of riparian wetlands in the transformation and emission of terrestrial carbon to the atmosphere. The considerable spatial heterogeneity of river deltas, however, forms a major obstacle for quantifying carbon emissions and their seasonality. The water chemistry in the river reaches is defined by the upstream catchment, whereas delta lakes and channels are dominated by local processes such as aquatic primary production, respiration or lateral exchange with the wetlands. In order to quantify carbon turnover and emissions in the complex mosaic of the Danube Delta, we conducted monthly field campaigns over 2 years at 19 sites spanning river reaches, channels and lakes. Here we report on the greenhouse gas fluxes (CO2 and CH4) from the freshwater systems of the Danube Delta and present the first seasonally resolved estimates of its freshwater carbon emissions to the atmosphere. Furthermore, we quantify the lateral carbon transport of the Danube River to the Black Sea. We estimate the delta's CO2 and CH4 emissions to be 65 GgC yr−1 (30–120 GgC yr−1, a range calculated using 25 to 75 percentiles of observed fluxes), of which about 8 % are released as CH4. The median CO2 fluxes from river branches, channels and lakes are 25, 93 and 5.8 mmol m−2 d−1, respectively. Median total CH4 fluxes amount to 0.42, 2.0 and 1.5 mmol m−2 d−1. While lakes do have the potential to act as CO2 sinks in summer, they are generally the largest emitters of CH4. Small channels showed the largest range in emissions, including a CO2 and CH4 hot spot sustained by adjacent wetlands. Thereby, the channels contribute disproportionately to the delta's emissions, considering their limited surface area. In terms of lateral export, we estimate the net total export (the sum of dissolved inorganic carbon, DIC, dissolved organic carbon, DOC, and particulate organic carbon, POC) from the Danube Delta to the Black Sea to be about 160 ± 280 GgC yr−1, which only marginally increases the carbon load from the upstream river catchment (8490 ± 240 GgC yr−1) by about 2 %. While this contribution from the delta seems small, deltaic carbon yield (45.6 gC m−2 yr−1; net export load/surface area) is about 4 times higher than the riverine carbon yield from the catchment (10.6 gC m−2 yr−1).ISSN:1726-4170ISSN:1726-417

Landscape Control on the Spatial and Temporal Variability of Chromophoric Dissolved Organic Matter and Dissolved Organic Carbon in Large African Rivers

The characteristics of colored dissolved organic matter (CDOM) as well as the concentrations and stable isotope composition (d 13 C) of dissolved organic carbon (DOC) were characterized in several large rivers of Africa including the Congo, Niger, Zambezi, and Ogooué basins. We compared the spatial and temporal patterns of dissolved organic matter (DOM) quantity and quality along with various environmental gradients, including hydrology, river size, catchment vegetation, and connectivity to land. The optical proxies used include the absorption coefficient at 350 nm, the specific ultraviolet absorbance, and the spectral slope ratio (S R = 275–295-nm slope divided by 350–400-nm slope). Our results show that land cover plays a primary role in controlling both DOC concentration and optical properties of DOM in tropical freshwaters. A higher cover of dense forest in the catchment leads to a higher quantity of highly aromatic DOM in the river network, whereas an increasing savannah cover results in lower DOC concentrations and less absorptive DOM. In addition to land cover, the watershed morphology (expressed by the average slope) exerts a strong control on DOC and CDOM in tropical rivers. Our results also show that the percentage of C3 and C4 vegetation cover is not an accurate predictor for DOM and CDOM quality in rivers due to the importance of the spatial distribution of land cover within the drainage network. The comparison of our results with previously published CDOM data in temperate and high-latitude rivers highlights that DOM in tropical freshwa-ters is generally more aromatic, and shows a higher capacity for absorbing sunlight irradiance.AFRIVA

Landscape heterogeneity influences carbon dioxide production in a young boreal reservoir

Surface carbon dioxide (CO2) emissions exhibit a high degree of spatial heterogeneity in the young boreal Eastmain-1 hydroelectric reservoir, located in northern Quebec, Canada. Estimates of the individual components of net CO2 production within the reservoir (benthic respiration, water column respiration, and primary production) furthermore provide a link between the heterogeneity in surface CO2 emissions and the flooded landscapes below. Specifically, the preflood carbon stock and soil–sediment respiration rates of flooded landscapes were found to influence benthic CO2 production, the rate of decline of hypolimnetic dissolved organic carbon (DOC), and the estimated rate at which flooded landscapes release DOC, further influencing water column respiration rates. Estimates of the individual components of net CO2 production in Eastmain-1 are supported by a positive relationship (t test, r2 = 0.64, P \u3c 0.01) between measured surface CO2 emissions (mean ± SE = 1540 ± 145.4 mg C·m–2·day–1) and independently derived estimates of total net CO2 production (mean ± SE = 1230 ± 162.4 mg C·m–2·day–1). Our findings emphasize the utility of fundamental landscape characterization prior to construction in predicting reservoir greenhouse gas emissions

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

© Author(s) 2015. 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.status: publishe