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See detailDynamics of greenhouse gases (CO2, CH4, N2O) along the Zambezi River and major tributaries, and their importance in the riverine carbon budget
Teodoru, C. R.; Nyoni, F. C.; Borges, Alberto ULg et al

in Biogeosciences (2015), 12(8), 2431-2453

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See detailTechnical Note: Large overestimation of pCO2 calculated from pH and alkalinity in acidic, organic-rich freshwaters
Abril, G; Bouillon, S; Darchambeau, François ULg et al

in Biogeosciences (2015), 12(1), 67-78

Inland waters have been recognized as a significant source of carbon dioxide (CO2) to the atmosphere at the global scale. Fluxes of CO2 between aquatic systems and the atmosphere are calculated from the ... [more ▼]

Inland waters have been recognized as a significant source of carbon dioxide (CO2) to the atmosphere at the global scale. Fluxes of CO2 between aquatic systems and the atmosphere are calculated from the gas transfer velocity and the water–air gradient of the partial pressure of CO2 (pCO2). Currently, direct measurements of water pCO2 remain scarce in freshwaters, and most published pCO2 data are calculated from temperature, pH and total alkalinity (TA). Here, we compare calculated (pH and TA) and measured (equilibrator and headspace) water pCO2 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 pCO2 (36 to 23 000 ppmv), and dissolved organic carbon (DOC) (29 to 3970 μmol L􀀀1). Calculated pCO2 were >10% higher than measured pCO2 in 60% of the samples (with a median overestimation of calculated pCO2 compared to measured pCO2 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 pCO2 with respect to measured pCO2 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 pCO2 to TA in acidic and organicrich waters. No empirical relationship could be derived from our data set in order to correct calculated pCO2 for this bias. Owing to the widespread distribution of acidic, organic-rich freshwaters, we conclude that regional and global estimates of CO2 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 pCO2 are recommended in inland waters in general, and in particular in acidic, poorly buffered freshwaters [less ▲]

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See detailMethanotrophy within the water column of a large meromictic tropical lake (Lake Kivu, East Africa)
Morana, C.; Borges, Alberto ULg; Roland, Fleur ULg et al

in Biogeosciences (2015), 12(7), 2077-2088

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See detailBiogeochemical processes and buffering capacity concurrently affect acidification in a seasonally hypoxic coastal marine basin
Hagens, M.; Slomp, C. P.; Meysman, F. J. R. et al

in Biogeosciences (2015), 12(5), 1561--1583

Coastal areas are impacted by multiple natural and anthropogenic processes and experience stronger pH fluctuations than the open ocean. These variations can weaken or intensify the ocean acidification ... [more ▼]

Coastal areas are impacted by multiple natural and anthropogenic processes and experience stronger pH fluctuations than the open ocean. These variations can weaken or intensify the ocean acidification signal induced by increasing atmospheric pCO2. The development of eutrophication-induced hypoxia intensifies coastal acidification, since the CO2 produced during respiration decreases the buffering capacity in any hypoxic bottom water. To assess the combined ecosystem impacts of acidification and hypoxia, we quantified the seasonal variation in pH and oxygen dynamics in the water column of a seasonally stratified coastal basin (Lake Grevelingen, the Netherlands). Monthly water-column chemistry measurements were complemented with estimates of primary production and respiration using O2 light–dark incubations, in addition to sediment–water fluxes of dissolved inorganic carbon (DIC) and total alkalinity (TA). The resulting data set was used to set up a proton budget on a seasonal scale. Temperature-induced seasonal stratification combined with a high community respiration was responsible for the depletion of oxygen in the bottom water in summer. The surface water showed strong seasonal variation in process rates (primary production, CO2 air–sea exchange), but relatively small seasonal pH fluctuations (0.46 units on the total hydrogen ion scale). In contrast, the bottom water showed less seasonality in biogeochemical rates (respiration, sediment–water exchange), but stronger pH fluctuations (0.60 units). This marked difference in pH dynamics could be attributed to a substantial reduction in the acid–base buffering capacity of the hypoxic bottom water in the summer period. Our results highlight the importance of acid–base buffering in the pH dynamics of coastal systems and illustrate the increasing vulnerability of hypoxic, CO2-rich waters to any acidifying process. [less ▲]

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See detailSoil redistribution and weathering controlling the fate of geochemical and physical carbon stabilization mechanisms in soils of an eroding landscape
Doetterl, Sebastien; Six, Johan; Bodé, Samuel et al

in Biogeosciences (2015)

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See detailCurrent systematic carbon-cycle observations and the need for implementing a policy-relevant carbon observing system
Ciais, P.; Dolman, A. J.; Bombelli, A. et al

in Biogeosciences (2014), 11(13), 3547--3602

A globally integrated carbon observation and analysis system is needed to improve the fundamental understanding of the global carbon cycle, to improve our ability to project future changes, and to verify ... [more ▼]

A globally integrated carbon observation and analysis system is needed to improve the fundamental understanding of the global carbon cycle, to improve our ability to project future changes, and to verify the effectiveness of policies aiming to reduce greenhouse gas emissions and increase carbon sequestration. Building an integrated carbon observation system requires transformational advances from the existing sparse, exploratory framework towards a dense, robust, and sustained system in all components: anthropogenic emissions, the atmosphere, the ocean, and the terrestrial biosphere. The paper is addressed to scientists, policymakers, and funding agencies who need to have a global picture of the current state of the (diverse) carbon observations.We identify the current state of carbon observations, and the needs and notional requirements for a global integrated carbon observation system that can be built in the next decade. A key conclusion is the substantial expansion of the ground-based observation networks required to reach the high spatial resolution for CO2 and CH4 fluxes, and for carbon stocks for addressing policy-relevant objectives, and attributing flux changes to underlying processes in each region. In order to establish flux and stock diagnostics over areas such as the southern oceans, tropical forests, and the Arctic, in situ observations will have to be complemented with remote-sensing measurements. Remote sensing offers the advantage of dense spatial coverage and frequent revisit. A key challenge is to bring remote-sensing measurements to a level of long-term consistency and accuracy so that they can be efficiently combined in models to reduce uncertainties, in synergy with groundbased data. Bringing tight observational constraints on fossil fuel and land use change emissions will be the biggest challenge for deployment of a policy-relevant integrated carbon observation system. This will require in situ and remotely sensed data at much higher resolution and density than currently achieved for natural fluxes, although over a small land area (cities, industrial sites, power plants), as well as the inclusion of fossil fuel CO2 proxy measurements such as radiocarbon in CO2 and carbon-fuel combustion tracers. Additionally, a policy-relevant carbon monitoring system should also provide mechanisms for reconciling regional top-down (atmosphere-based) and bottom-up (surface-based) flux estimates across the range of spatial and temporal scales relevant to mitigation policies. In addition, uncertainties for each observation data-stream should be assessed. The success of the system will rely on long-term commitments to monitoring, on improved international collaboration to fill gaps in the current observations, on sustained efforts to improve access to the different data streams and make databases interoperable, and on the calibration of each component of the system to agreed-upon international scales. [less ▲]

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See detailDynamic seasonal nitrogen cycling in response to anthropogenic N loading in a tropical catchment, Athi–Galana–Sabaki River, Kenya
Marwick, T. R.; Tamooh, F.; Ogwoka, B. et al

in Biogeosciences (2014), 11(2), 443--460

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See detailInsights into oxygen transport and net community production in sea ice from oxygen, nitrogen and argon concentrations
Zhou, Jiayun ULg; Delille, Bruno ULg; Brabant, F. et al

in Biogeosciences (2014), 11

We present the evolution of O2 standing stocks, saturation levels and concentrations in landfast sea ice, collected in Barrow (Alaska), from February to June 2009. The comparison of the standing stocks ... [more ▼]

We present the evolution of O2 standing stocks, saturation levels and concentrations in landfast sea ice, collected in Barrow (Alaska), from February to June 2009. The comparison of the standing stocks and saturation levels of O2 against those of N2 and Ar suggests that the dynamic of O2 in sea ice strongly depends on physical processes (gas incorporation and subsequent transport). We then discuss on the use of O2 / Ar and O2 / N2 to correct for the physical contribution and to determine the biological contribution (NCP) to O2 supersaturations. We conclude that O2 / Ar suits better than O2 / N2, because O2 / N2 is more sensitive due to the relative abundance of O2, N2 and Ar, and less biased when gas bubble formation and gas diffusion are maximized. We further estimate the NCP in the impermeable layers during ice growth and in the permeable layers during ice decay. Our results indicate that NCP contributed to a~release of carbon to the atmosphere in the upper ice layers, but to an uptake of carbon at sea ice bottom. Overall, seawater (rather than the atmosphere) may be the main supplier of carbon for sea ice microorganisms. [less ▲]

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See detailCO2 and CH4 in sea ice from a subarctic fjord under influence of riverine input
Crabeck, O.; Delille, Bruno ULg; Thomas, David et al

in Biogeosciences (2014), 11(23), 6525--6538

We present the CH4 concentration [CH4], the par- tial pressure of CO2 (pCO2) and the total gas content in bulk sea ice from subarctic, land-fast sea ice in the Kapisillit fjord, Greenland. Fjord systems ... [more ▼]

We present the CH4 concentration [CH4], the par- tial pressure of CO2 (pCO2) and the total gas content in bulk sea ice from subarctic, land-fast sea ice in the Kapisillit fjord, Greenland. Fjord systems are characterized by freshwater runoff and riverine input and based on $\delta$18O data, we show that >30\% of the surface water originated from periodic river input during ice growth. This resulted in fresher sea-ice layers with higher gas content than is typical from marine sea ice. The bulk ice [CH4] ranged from 1.8 to 12.1 nmolL−1, which corresponds to a partial pressure ranging from 3 to 28ppmv. This is markedly higher than the average atmo- spheric methane content of 1.9ppmv. Evidently most of the trapped methane within the icewas contained inside bubbles, and only a minor portion was dissolved in the brines. The bulk ice pCO2 ranged from 60 to 330ppmv indicating that sea ice at temperatures above −4 ◦C is undersaturated com- pared to the atmosphere (390 ppmv). This study adds to the few existing studies of CH4 and CO2 in sea ice, and we con- clude that subarctic seawater can be a sink for atmospheric CO2, while being a net source of CH4. [less ▲]

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See detailRates of consumption of atmospheric CO2 through the weathering of loess during the next 100 yr of climate change
Goddéris, Y.; Brantley, S. L.; François, Louis ULg et al

in Biogeosciences (2013), 10

Quantifying how C fluxes will change in the future is a complex task for models because of the coupling between climate, hydrology, and biogeochemical reactions. Here we investigate how pedogenesis of the ... [more ▼]

Quantifying how C fluxes will change in the future is a complex task for models because of the coupling between climate, hydrology, and biogeochemical reactions. Here we investigate how pedogenesis of the Peoria loess, which has been weathering for the last 13 kyr, will respond over the next 100 yr of climate change. Using a cascade of numerical models for climate (ARPEGE), vegetation (CARAIB) and weathering (WITCH), we explore the effect of an increase in CO2 of 315 ppmv (1950) to 700 ppmv (2100 projection). The increasing CO2 results in an increase in temperature along the entire transect. In contrast, drainage increases slightly for a focus pedon in the south but decreases strongly in the north. These two variables largely determine the behavior of weathering. In addition, although CO2 production rate increases in the soils in response to global warming, the rate of diffusion back to the atmosphere also increases, maintaining a roughly constant or even decreasing CO2 concentration in the soil gas phase. Our simulations predict that temperature increasing in the next 100 yr causes the weathering rates of the silicates to increase into the future. In contrast, the weathering rate of dolomite – which consumes most of the CO2 – decreases in both end members (south and north) of the transect due to its retrograde solubility. We thus infer slower rates of advance of the dolomite reaction front into the subsurface, and faster rates of advance of the silicate reaction front. However, additional simulations for 9 pedons located along the north–south transect show that the dolomite weathering advance rate will increase in the central part of the Mississippi Valley, owing to a maximum in the response of vertical drainage to the ongoing climate change. The carbonate reaction front can be likened to a terrestrial lysocline because it represents a depth interval over which carbonate dissolution rates increase drastically. However, in contrast to the lower pH and shallower lysocline expected in the oceans with increasing atmospheric CO2, we predict a deeper lysocline in future soils. Furthermore, in the central Mississippi Valley, soil lysocline deepening accelerates but in the south and north the deepening rate slows. This result illustrates the complex behavior of carbonate weathering facing short term global climate change. Predicting the global response of terrestrial weathering to increased atmospheric CO2 and temperature in the future will mostly depend upon our ability to make precise assessments of which areas of the globe increase or decrease in precipitation and soil drainage. [less ▲]

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See detailDynamics of dissolved inorganic carbon and aquatic metabolism in the Tana River basin, Kenya
Tamooh, F.; Borges, Alberto ULg; Meysman, F. J. R. et al

in Biogeosciences (2013), 10(11), 6911-6928

A basin-wide study was conducted in the Tana River basin (Kenya) in February 2008 (dry season), September–November 2009 (wet season) and June– July 2010 (end of the wet season) to assess the dynamics and ... [more ▼]

A basin-wide study was conducted in the Tana River basin (Kenya) in February 2008 (dry season), September–November 2009 (wet season) and June– July 2010 (end of the wet season) to assess the dynamics and sources of dissolved inorganic carbon (DIC) as well as to quantify CO2 fluxes, community respiration (R), and primary production (P). Samples were collected along the altitudinal gradient (from 3600 to 8 m) in several headwater streams, reservoirs (Kamburu and Masinga), and the Tana River mainstream. DIC concentrations ranged from 0.2 to 4.8 mmol L−1, with exceptionally high values (3.5±1.6 mmol L−1) in Nyambene Hills tributaries. The wide range of 13CDIC values (−15.0 to −2.4 ‰) indicate variable sources of DIC, with headwater streams recording more positive signatures compared to the Tana River mainstream. With with only a few exceptions, the entire riverine network was supersaturated in CO2, implying the system is a net source of CO2 to the atmosphere. pCO2 values were generally higher in the lower Tana River mainstream compared to headwater tributaries, opposite to the pattern typically observed in other river networks. This was attributed to high suspended sediment in the Tana River mainstream fuelling in-stream community respiration and net heterotrophy. This was particularly evident during the 2009 wet season campaign (median pCO2 of 1432 ppm) compared to the 2010 end of the wet season (1002 ppm) and 2008 dry season(579 ppm). First-order estimates show that in-stream community respiration was responsible for the bulk of total CO2 evasion (77 to 114 %) in the Tana River mainstream, while in the tributaries, this could only account for 5 to 68% of total CO2 evasion. This suggests that CO2 evasion in the tributaries was to a substantial degree sustained by benthic mineralisation and/or lateral inputs of CO2-oversaturated groundwater. While sediment loads increased downstream and thus light availability decreased in the water column, both chlorophyll a (0.2 to 9.6 μg L−1) and primary production (0.004 to 7.38 μmol CL−1 h−1) increased consistently downstream. Diurnal fluctuations of biogeochemical processes were examined at three different sites along the river continuum (headwater, reservoir and mainstream), and were found to be substantial only in the headwater stream, moderate in the reservoir and not detectable in the Tana River mainstream. The pronounced diurnal fluctuations observed in the headwater stream were largely regulated by periphyton as deduced from the low chlorophyll a in the water column. [less ▲]

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See detailDrivers, mechanisms and long-term variability of seasonal hypoxia on the Black Sea northwestern shelf – is there any recovery after eutrophication?
Capet, Arthur ULg; Beckers, Jean-Marie ULg; Grégoire, Marilaure ULg

in Biogeosciences (2013), 10

The Black Sea northwestern shelf (NWS) is a shallow eutrophic area in which the seasonal stratification of the water column isolates the bottom waters from the atmosphere. This prevents ventilation from ... [more ▼]

The Black Sea northwestern shelf (NWS) is a shallow eutrophic area in which the seasonal stratification of the water column isolates the bottom waters from the atmosphere. This prevents ventilation from counterbalancing the large consumption of oxygen due to respiration in the bottom waters and in the sediments, and sets the stage for the development of seasonal hypoxia. A three-dimensional (3-D) coupled physical–biogeochemical model is used to investigate the dynamics of bottom hypoxia in the Black Sea NWS, first at seasonal and then at interannual scales (1981–2009), and to differentiate its driving factors (climatic versus eutrophication). Model skills are evaluated by a quantitative comparison of the model results to 14 123 in situ oxygen measurements available in the NOAA World Ocean and the Black Sea Commission databases, using different error metrics. This validation exercise shows that the model is able to represent the seasonal and interannual variability of the oxygen concentration and of the occurrence of hypoxia, as well as the spatial distribution of oxygen-depleted waters. During the period 1981–2009, each year exhibits seasonal bottom hypoxia at the end of summer. This phenomenon essentially covers the northern part of the NWS – which receives large inputs of nutrients from the Danube, Dniester and Dnieper rivers – and extends, during the years of severe hypoxia, towards the Romanian bay of Constanta. An index H which merges the aspects of the spatial and temporal extension of the hypoxic event is proposed to quantify, for each year, the intensity of hypoxia as an environmental stressor. In order to explain the interannual variability of H and to disentangle its drivers, we analyze the long time series of model results by means of a stepwise multiple linear regression. This statistical model gives a general relationship that links the intensity of hypoxia to eutrophication and climate-related variables. A total of 82% of the interannual variability of H is explained by the combination of four predictors: the annual riverine nitrate load (N), the sea surface temperature in the month preceding stratification (Ts), the amount of semi-labile organic matter accumulated in the sediments (C) and the sea surface temperature during late summer (Tf). Partial regression indicates that the climatic impact on hypoxia is almost as important as that of eutrophication. Accumulation of organic matter in the sediments introduces an important inertia in the recovery process after eutrophication, with a typical timescale of 9.3 yr. Seasonal fluctuations and the heterogeneous spatial distribution complicate the monitoring of bottom hypoxia, leading to contradictory conclusions when the interpretation is done from different sets of data. In particular, it appears that the recovery reported in the literature after 1995 was overestimated due to the use of observations concentrated in areas and months not typically affected by hypoxia. This stresses the urgent need for a dedicated monitoring effort in the Black Sea NWS focused on the areas and months concerned by recurrent hypoxic events. [less ▲]

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See detailDistribution and origin of suspended matter and organic carbon pools in the Tana River Basin, Kenya
Tamooh, F; Van den Meersche, K; Meysman, F et al

in Biogeosciences (2012), 9

We studied patterns in organic carbon pools and their origin in the Tana River Basin (Kenya), in February 2008 (dry season), September–November 2009 (wet season), and June–July 2010 (end of wet season ... [more ▼]

We studied patterns in organic carbon pools and their origin in the Tana River Basin (Kenya), in February 2008 (dry season), September–November 2009 (wet season), and June–July 2010 (end of wet season), covering the full continuum from headwater streams to lowland mainstream sites. A consistent downstream increase in total suspended matter (TSM, 0.6 to 7058 mg l−1) and particulate organic carbon (POC, 0.23 to 119.8 mg l−1) was observed during all three sampling campaigns, particularly pronounced below 1000m above sea level, indicating that most particulate matter exported towards the coastal zone originated from the mid and low altitude zones rather than from headwater regions. This indicates that the cascade of hydroelectrical reservoirs act as an extremely efficient particle trap. Although 7Be / 210Pbxs ratios/age of suspended sediment do not show clear seasonal variation, the gradual downstream increase of suspended matter during end of wet season suggests its origin is caused by inputs of older sediments from bank erosion and/or river sediment resuspension. During wet season, higher TSM concentrations correspond with relatively young suspended matter, suggesting a contribution from recently eroded material.With the exception of reservoir waters, POC was predominantly of terrestrial origin as indicated by generally high POC : chlorophyll a (POC : Chl a) ratios (up to 41 000). Stable isotope signatures of POC ( 13CPOC) ranged between −32 and −20‰and increased downstream, reflecting an increasing contribution of C4-derived carbon in combination with an expected shift in 13C for C3 vegetation towards the more semi-arid lowlands. 13C values in sediments from the main reservoir (−19.5 to −15.7 ‰) were higher than those found in any of the riverine samples, indicating selective retention of particles associated with C4 fraction. Dissolved organic carbon (DOC) concentrations were highest during the end of wet season (2.1 to 6.9 mg l−1), with stable isotope signatures generally between −28 and −22 ‰. A consistent downstream decrease in % organic carbon (%OC) was observed for soils, riverine sediments, and suspended matter. This was likely due to better preservation of the organic fraction in colder high altitude regions, with loss of carbon during downstream spiraling. 13C values for soil and sediment did not exhibit clear altitudinal patterns, but values reflect the full spectrum from C3-dominated to C4-dominated sites. Very low ratios of organic carbon to mineral surface area (OC : SA) were found in reservoir sediments and suspended matter in the lower Tana River, indicating that these are stable OC pools which have undergone extensive degradation. Overall, our study demonstrates that substantial differences occur in both the quantities and origin of suspended sediments and organic carbon along the river profile in this tropical river basin, as well as seasonal differences in the mechanisms causing such variations. [less ▲]

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See detailOrganic matter sources, fluxes and greenhouse gas exchange in the Oubangui River (Congo River basin)
Bouillon, S.; Yambélé, A.; Spencer, R.G.M. et al

in Biogeosciences (2012), 9

The Oubangui is a major tributary of the Congo River, draining an area of 500 000 km2 mainly consisting of wooded savannahs. Here, we report results of a one year long, 2-weekly sampling campaign in ... [more ▼]

The Oubangui is a major tributary of the Congo River, draining an area of 500 000 km2 mainly consisting of wooded savannahs. Here, we report results of a one year long, 2-weekly sampling campaign in Bangui (Central African Republic) since March 2010 for a suite of physicochemical and biogeochemical characteristics, including total suspended matter (TSM), bulk concentration and stable isotope composition of particulate organic carbon (POC and 13CPOC), particulate nitrogen (PN and 15NPN), dissolved organic carbon (DOC and 13CDOC), dissolved inorganic carbon (DIC and 13CDIC), dissolved greenhouse gases (CO2, CH4 and N2O), and dissolved ignin composition. 13C signatures of both POC and DOC showed strong seasonal variations −30.6 to −25.8 ‰, and −31.8 to −27.1 ‰, respectively), but their different timing indicates that the origins of POC and DOC may vary strongly over the hydrograph and are largely ncoupled, differing up to 6‰ in 13C signatures. Dissolved lignin characteristics (carbon- ormalised yields, cinnamyl:vanillyl phenol ratios, and vanillic acid to vanillin ratios) showed arked differences between high and low discharge conditions, consistent with major seasonal ariations in the sources of dissolved organic matter. We observed a strong seasonality in pCO2, ranging between 470 ± 203 ppm for Q<1000m3 s−1 (n = 10) to a maximum of 3750 pm during the first stage of the rising discharge. The low POC/PN ratios, high %POCand low and variable 13CPOC signatures during low flow conditions suggest that the majority of the POC pool during this period consists of in situ produced phytoplankton, consistent with oncurrent pCO2 (partial pressure of CO2) values only slightly above and, occasionally, below atmospheric equilibrium. Water-atmosphere CO2 fluxes estimated using two independent pproaches averaged 105 and 204 gCm−2 yr−1, i.e. more than an order of magnitude lower than current estimates for large tropical rivers globally. Although tropical rivers are often ssumed to show much higher CO2 effluxes compared to temperate systems, we show that in situ production may be high enough to dominate the particulate organic carbon pool, and lower CO2 values to near equilibrium values during low discharge conditions. The total annual flux of TSM, POC, PN, DOC and DIC are 2.33 Tg yr−1, 0.14 TgC yr−1, 0.014 TgNyr−1, 0.70 TgC yr−1, and 0.49 Tg Cyr−1, respectively. While our TSM and POC fluxes are similar to previous stimates for the Oubangui, DOC fluxes were 30% higher and bicarbonate fluxes were 35% ower than previous reports. DIC represented 58% of the total annual C flux, and under the ssumptions that carbonate weathering represents 25% of the DIC flux and that CO2 from espiration drives chemical weathering, this flux is equivalent to 50% of terrestrial-derived riverine C transport. [less ▲]

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See detailSpatial and temporal CO2 exchanges measured by Eddy Covariance over a temperate intertidal flat and their relationships to net ecosystem production
Polsenaere, P.; Lamaud, E.; Lafon, V. et al

in Biogeosciences (2012), 9(1), 249--268

Measurements of carbon dioxide fluxes were performed over a temperate intertidal mudflat in southwestern France using the micrometeorological Eddy Covariance (EC) technique. EC measurements were carried ... [more ▼]

Measurements of carbon dioxide fluxes were performed over a temperate intertidal mudflat in southwestern France using the micrometeorological Eddy Covariance (EC) technique. EC measurements were carried out in two contrasting sites of the Arcachon flat during four periods and in three different seasons (autumn 2007, summer 2008, autumn 2008 and spring 2009). In addition, satellite images of the tidal flat at low tide were used to link the net ecosystem CO2 exchange (NEE) with the occupation of the mudflat by primary producers, particularly by Zostera noltii meadows. CO2 fluxes during the four deployments showed important spatial and temporal variations, with the flat rapidly shifting from sink to source with the tide. Absolute CO2 fluxes showed generally small negative (influx) and positive (efflux) values, with larger values up to −13 μmol m−2 s−1 for influxes and 19 μmol m−2 s−1 for effluxes. Low tide during the day was mostly associated with a net uptake of atmospheric CO2. In contrast, during immersion and during low tide at night, CO2 fluxes where positive, negative or close to zero, depending on the season and the site. During the autumn of 2007, at the innermost station with a patchy Zostera noltii bed (cover of 22 ± 14% in the wind direction of measurements), CO2 influx was −1.7 ± 1.7 μmol m−2 s−1 at low tide during the day, and the efflux was 2.7 ± 3.7 μmol m−2 s−1 at low tide during the night. A gross primary production (GPP) of 4.4 ± 4.1 μmol m−2 s−1 during emersion could be attributed to microphytobenthic communities. During the summer and autumn of 2008, at the central station with a dense eelgrass bed (92 ± 10%), CO2 uptakes at low tide during the day were −1.5 ± 1.2 and −0.9 ± 1.7 μmol m−2 s−1, respectively. Night time effluxes of CO2 were 1.0 ± 0.9 and 0.2 ± 1.1 μmol m−2 s−1 in summer and autumn, respectively, resulting in a GPP during emersion of 2.5 ± 1.5 and 1.1 ± 2.0 μmol m−2 s−1, respectively, attributed primarily to the seagrass community. At the same station in April 2009, before Zostera noltii started to grow, the CO2 uptake at low tide during the day was the highest (−2.7 ± 2.0 μmol m−2 s−1). Influxes of CO2 were also observed during immersion at the central station in spring and early autumn and were apparently related to phytoplankton blooms occurring at the mouth of the flat, followed by the advection of CO2-depleted water with the flooding tide. Although winter data as well as water carbon measurements would be necessary to determine a precise CO2 budget for the flat, our results suggest that tidal flat ecosystems are a modest contributor to the CO2 budget of the coastal ocean. [less ▲]

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See detailCarbonate system in the water masses of the Southeast Atlantic sector of the Southern Ocean during February and March 2008
Gonzalez-Davila, M.; Santana-Casiano, J. M.; Fine, R. A. et al

in Biogeosciences (2011), 8

Carbonate system variables were measured in the South Atlantic sector of the Southern Ocean along a transect from South Africa to the southern limit of the Antarctic Circumpolar Current (ACC) from ... [more ▼]

Carbonate system variables were measured in the South Atlantic sector of the Southern Ocean along a transect from South Africa to the southern limit of the Antarctic Circumpolar Current (ACC) from February to March 2008. Eddies detached from the retroflection of the Agulhas Current increased the gradients observed along the fronts. Minima in the fugacity of CO2, fCO2, and maxima in pH on either side of the frontal zone were observed, noting that within the frontal zone fCO2 reached maximum values and pH was at a minimum. Vertical distributions of water masses were described by their carbonate system properties and their relationship to CFC concentrations. Upper Circumpolar Deep Water (UCDW) and Lower Circumpolar Deep Water (LCDW) offered pHT,25 values of 7.56 and 7.61, respectively. The UCDW also had higher concentrations of CFC-12 (>0.2 pmol kg−1) as compared to deeper waters, revealing that UCDW was mixed with recently ventilated waters. Calcite and aragonite saturation states (Ω) were also affected by the presence of these two water masses with high carbonate concentrations. The aragonite saturation horizon was observed at 1000 m in the subtropical area and north of the Subantarctic Front. At the position of the Polar Front, and under the influence of UCDW and LCDW, the aragonite saturation horizon deepened from 800 m to 1500 m at 50.37° S, and reached 700 m south of 57.5° S. High latitudes proved to be the most sensitive areas to predicted anthropogenic carbon increase. Buffer coefficients related to changes in [CO2], [H+] and Ω with changes in dissolved inorganic carbon (CT) and total alkalinity (AT) offered minima values in the Antarctic Intermediate Water and UCDW layers. These coefficients suggest that a small increase in CT will sharply decrease the status of pH and carbonate saturation. Here we present data that suggest that south of 55° S, surface water will be under-saturated with respect to aragonite within the next few decades. [less ▲]

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See detailTracing the origin of dissolved silicon transferred from various soil-plant systems towards rivers: a review
Cornelis, Jean-Thomas ULg; Delvaux, Bruno; Georg, Bastian et al

in Biogeosciences (2011), 8

Abstract : Silicon (Si) released as H4SiO4 by weathering of Si-containing solid phases is partly recycled through vegetation before its land-to-rivers transfer. By accumulating in terrestrial plants to a ... [more ▼]

Abstract : Silicon (Si) released as H4SiO4 by weathering of Si-containing solid phases is partly recycled through vegetation before its land-to-rivers transfer. By accumulating in terrestrial plants to a similar extent as some major macronutrients(0.1–10% Si dry weight), Si becomes largely mobile in the soil-plant system. Litter-fall leads to a substantial reactive biogenic silica pool in soil, which contributes to the release of dissolved Si (DSi) in soil solution. Understanding the biogeochemical cycle of silicon in surface environments and the DSi export from soils into rivers is crucial given that the marine primary bio-productivity depends on the availability of H4SiO4 for phytoplankton that requires Si. Continental fluxes of DSi seem to be deeply influenced by climate (temperature and runoff) as well as soil-vegetation systems. Therefore, continental areas can be characterized by various abilities to transfer DSi from soil-plant systems towards rivers. Here we pay special attention to those processes taking place in soil-plant systems and controlling the Si transfer towards rivers. We aim at identifying relevant geochemical tracers of Si pathways within the soil-plant system to obtain a better understanding of the origin of DSi exported towards rivers. In this review, we compare different soilplant systems (weathering-unlimited and weathering-limited environments) and the variations of the geochemical tracers(Ge/Si ratios and 30Si) in DSi outputs. We recommend the use of biogeochemical tracers in combination with Si massbalances and detailed physico-chemical characterization of soil-plant systems to allow better insight in the sources and fate of Si in these biogeochemical systems. [less ▲]

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See detailIndividual and interacting effects of pCO2 and temperature on Emiliania huxleyi calcification: Study of the calcite production, the coccolith morphology and the coccosphere size
De Bodt, Caroline; Van Oostende, Nicolas; Harlay, Jérôme ULg et al

in Biogeosciences (2010), 7

The impact of ocean acidification and increased water temperature on marine ecosystems, in particular those involving calcifying organisms, has been gradually recognised. We examined the individual and ... [more ▼]

The impact of ocean acidification and increased water temperature on marine ecosystems, in particular those involving calcifying organisms, has been gradually recognised. We examined the individual and combined effects of increased pCO2 (180 ppm V CO2, 380 ppm V CO2 and 750 ppm V CO2 corresponding to past, present and future CO2 conditions, respectively) and temperature (13°C and 18°C) during the calcification phase of the coccolithophore E. huxleyi using batch culture experiments. We showed that the cell abundance-normalized particulate organic carbon concentration (POC) increased from the present to the future CO2 treatments. A significant effect of pCO2 and of temperature on calcification was found, manifesting itself in a lower cell abundance-normalized particulate inorganic carbon (PIC) content as well as a lower PIC:POC ratio at future CO2 levels and at 18°C. Coccosphere-sized particles showed a size reduction trend with both increasing temperature and CO2 concentration. The influence of the different treatments on coccolith morphology was studied by categorizing SEM coccolith micrographs. The number of well-formed coccoliths decreased with increasing pCO2 while temperature did not have a significant impact on coccolith morphology. No interacting effect of pCO2 and temperature was observed on calcite production, coccolith morphology or on coccosphere size. Finally, our results suggest that ocean acidification might have a larger adverse impact on coccolithophorid calcification than surface water warming. [less ▲]

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See detailThe role of ocean transport in the uptake of anthropogenic CO2
Cao, L.; Eby, M.; Ridgwell, A. et al

in Biogeosciences (2009), 6(3), 375-390

We compare modeled oceanic carbon uptake in response to pulse CO2 emissions using a suite of global ocean models and Earth system models. In response to a CO2 pulse emission of 590 Pg C (corresponding to ... [more ▼]

We compare modeled oceanic carbon uptake in response to pulse CO2 emissions using a suite of global ocean models and Earth system models. In response to a CO2 pulse emission of 590 Pg C (corresponding to an instantaneous doubling of atmospheric CO2 from 278 to 556 ppm), the fraction of CO2 emitted that is absorbed by the ocean is: 37 +/- 8\%, 56 +/- 10\%, and 81 +/- 4 (model mean +/- 2 sigma) in year 30, 100, and 1000 after the emission pulse, respectively. Modeled oceanic uptake of pulse CO2 on timescales from decades to about a century is strongly correlated with simulated present-day uptake of chlorofluorocarbons (CFCs) and CO2 across all models, while the amount of pulse CO2 absorbed by the ocean from a century to a millennium is strongly correlated with modeled radiocarbon in the deep Southern and Pacific Ocean. However, restricting the analysis to models that are capable of reproducing observations within uncertainty, the correlation is generally much weaker. The rates of surface-to-deep ocean transport are determined for individual models from the instantaneous doubling CO2 simulations, and they are used to calculate oceanic CO2 uptake in response to pulse CO2 emissions of different sizes pulses of 1000 and 5000 Pg C. These results are compared with simulated oceanic uptake of CO2 by a number of models simulations with the coupling of climate-ocean carbon cycle and without it. This comparison demonstrates that the impact of different ocean transport rates across models on oceanic uptake of anthropogenic CO2 is of similar magnitude as that of climate-carbon cycle feed-backs in a single model, emphasizing the important role of ocean transport in the uptake of anthropogenic CO2. [less ▲]

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See detailDistribution, origin and cycling of carbon in the Tana River (Kenya): a dry season basin-scale survey from headwaters to the delta
Bouillon, S.; Abril, G.; Borges, Alberto ULg et al

in Biogeosciences (2009), 6

The Tana River basin (TRB) is the largest in Kenya (_120 000 km2). We conducted a survey during the dry season throughout the TRB, analyzing a broad suite of biogeochemical parameters. Biogeochemical ... [more ▼]

The Tana River basin (TRB) is the largest in Kenya (_120 000 km2). We conducted a survey during the dry season throughout the TRB, analyzing a broad suite of biogeochemical parameters. Biogeochemical signatures in headwater streams were highly variable. Along the middle and lower river course, total suspended matter (TSM) concentrations increased more than 30-fold despite the absence of tributary inputs, indicating important resuspension events of internally stored sediment. These resuspended sediment inputs were characterized by a lower and 14C-depleted OC content, suggesting selective degradation of more recent material during sediment retention. Masinga Dam (a large reservoir on the upper river) induced a strong nutrient retention (_50% for inorganic N, _72% for inorganic phosphate, and _40% for dissolved silicate). Moreover, while DOC pools and _13C signatures were similar above, in and below the reservoir, the POC pool in Masinga surface waters was dominated by 13C-depleted phytoplankton, which contributed to the riverine POC pool immediately below the dam, but rapidly disappeared further downstream, suggesting rapid remineralization of this labile C pool in the river system. Despite the generally high turbidity, the combination of relatively high oxygen saturation levels, low _18O signatures of dissolved O2 (all <+24.2‰), and the relatively low pCO2 values suggest that in-stream primary production was significant, even though pigment data suggest that phytoplankton makes only a minor contribution to the total POC pool in the Tana River. [less ▲]

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