Origin and cycling of riverine inorganic carbon in the Sava River watershed (Slovenia) inferred from major solutes and stable carbon isotopes

The Sava River and its tributaries in Slovenia represent waters strongly influenced by chemical weathering of limestone and dolomite. The carbon isotopic compositions of dissolved inorganic carbon (DIC) and suspended organic carbon (POC) fractions as well as major solute concentrations yielded insights into the origin and fluxes of carbon in the upper Sava River system. The major solute composition was dominated by carbonic acid dissolution of calcite and dolomite. Waters were generally supersaturated with respect to calcite, and dissolved CO₂ was about fivefold supersaturated relative to the atmosphere. The δ¹³C of DIC ranged from −13.5 to −3.3‰. Mass balances for riverine inorganic carbon suggest that carbonate dissolution contributes up to 26%, degradation of organic matter ∼17% and exchange with atmospheric CO₂ up to 5%. The concentration and stable isotope diffusion models indicated that atmospheric exchange of CO₂ predominates in streams draining impermeable shales and clays while in the carbonate-dominated watersheds dissolution of the Mesozoic carbonates predominates.     

Oxygen inhibition of dissolved inorganic carbon uptake in unicellular green algae

Unicellular green algae have a dissolved inorganic carbon (DIC) concentrating mechanism, commonly known as the DIC pump, to concentrate inorganic carbon into cells and chloroplasts. The DIC pump activity is normally measured as the K_0.5(DIC) that equals the CO₂ plus HCO₃‐ concentration at a cited pH at which the rate of DIC‐dependent photosynthetic O₂ evolution is half‐maximal, or by the amount of intra‐cellular DIC accumulation in 15–60 s, using a limited amount of NaH¹⁴CO₃, measured by the silicone oil cen‐trifugation technique. The dissolved oxygen in the assay inhibits or reduces the DIC uptake by the cells of unicellular green algae Chlamydomonas reinhardtii Dangeard, strain 137 and in a cell wall‐less marine algae Dunaliella tertiolecta Butcher. The algal cells concentrated the highest amount of DIC when little or no oxygen was present in the assay medium. The results suggest that the amount of O₂ and DIC must be carefully monitored before DIC‐pump assay.     

Inorganic carbon promotes photosynthesis,growth, and maximum biomass of phytoplankton in eutrophic water bodies

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Evasion of CO2 from streams – The dominant component of the carbon export through the aquatic conduit in a boreal landscape

Evasion of gaseous carbon (C) from streams is often poorly quantified in landscape C budgets. Even though the potential importance of the capillary network of streams as C conduits across the land–water–atmosphere interfaces is sometimes mentioned, low‐order streams are often left out of budget estimates due to being poorly characterized in terms of gas exchange and even areal surface coverage. We show that evasion of C is greater than all the total dissolved C (both organic and inorganic) exported downstream in the waters of a boreal landscape. In this study evasion of carbon dioxide (CO₂) from running waters within a 67 km² boreal catchment was studied. During a 4 year period (2006–2009) 13 streams were sampled on 104 different occasions for dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC). From a locally determined model of gas exchange properties, we estimated the daily CO₂ evasion with a high‐resolution (5 × 5 m) grid‐based stream evasion model comprising the entire ~100 km stream network. Despite the low areal coverage of stream surface, the evasion of CO₂ from the stream network constituted 53% (5.0 (±1.8) g C m^?2 yr^?1) of the entire stream C flux (9.6 (±2.4) g C m^?2 yr^?1) (lateral as DIC, DOC, and vertical as CO₂). In addition, 72% of the total CO₂ loss took place already in the first‐ and second‐order streams. This study demonstrates the importance of including CO₂ evasion from low‐order boreal streams into landscape C budgets as it more than doubled the magnitude of the aquatic conduit for C from this landscape. Neglecting this term will consequently result in an overestimation of the terrestrial C sink strength in the boreal landscape.     

Fluvial transport of carbon along the river-to-ocean continuum and its potential impacts on a brackish water food web in the Iwaki River watershed, northern Japan

Riverine transport of dissolved inorganic carbon (DIC) from land to the ocean is an important carbon flux that influences the carbon budget at the watershed scale. However, the dynamics of DIC in an entire river network has remained unknown, especially in mountainous Japanese watersheds. We examined the effects of watershed land use and geology on the transports of inorganic carbon as well as weathered silica (Si) and calcium (Ca) in the Iwaki River system where agricultural and residential areas have developed in the middle and lower parts of the watershed. The concentration and stable carbon isotope ratios (δ¹³C) of DIC showed the longitudinal increase of ¹³C-depleted inorganic carbon along the river. As a result, most streams and rivers were supersaturated in dissolved CO₂ that will eventually be emitted to the atmosphere. The possible origin of ¹³C-depleted carbon is CO₂ derived from the decomposition of organic matter in agricultural and urban landscapes, as well as from in-stream respiration. In addition, agricultural and urban areas, respectively, exported the large amount of dissolved Si and Ca to the rivers, suggesting that CO₂ increased by respiration accelerates the chemical weathering of silicate and carbonate materials in soils, river sediments, and/or urban infrastructure. Furthermore, riverine bicarbonate flux is likely to enter shell carbonates of Corbicula japonica, an aragonitic bivalve, in the downstream brackish lake (Lake Jusan). These results revealed that the flux of DIC from the human-dominated watersheds is a key to understanding the carbon dynamics and food-web structure along the land-to-river-to-ocean continuum.     

Carbon Cycling of Lake Kivu (East Africa): Net Autotrophy in the Epilimnion and Emission of CO2 to the Atmosphere Sustained by Geogenic Inputs

We report organic and inorganic carbon distributions and fluxes in a large (>2000 km²) oligotrophic, tropical lake (Lake Kivu, East Africa), acquired during four field surveys, that captured the seasonal variations (March 2007–mid rainy season, September 2007–late dry season, June 2008–early dry season, and April 2009–late rainy season). The partial pressure of CO₂ (pCO₂) in surface waters of the main basin of Lake Kivu showed modest spatial (coefficient of variation between 3% and 6%), and seasonal variations with an amplitude of 163 ppm (between 579±23 ppm on average in March 2007 and 742±28 ppm on average in September 2007). The most prominent spatial feature of the pCO₂ distribution was the very high pCO₂ values in Kabuno Bay (a small sub-basin with little connection to the main lake) ranging between 11213 ppm and 14213 ppm (between 18 and 26 times higher than in the main basin). Surface waters of the main basin of Lake Kivu were a net source of CO₂ to the atmosphere at an average rate of 10.8 mmol m⁻² d⁻¹, which is lower than the global average reported for freshwater, saline, and volcanic lakes. In Kabuno Bay, the CO₂ emission to the atmosphere was on average 500.7 mmol m⁻² d⁻¹ (∼46 times higher than in the main basin). Based on whole-lake mass balance of dissolved inorganic carbon (DIC) bulk concentrations and of its stable carbon isotope composition, we show that the epilimnion of Lake Kivu was net autotrophic. This is due to the modest river inputs of organic carbon owing to the small ratio of catchment area to lake surface area (2.15). The carbon budget implies that the CO₂ emission to the atmosphere must be sustained by DIC inputs of geogenic origin from deep geothermal springs.     

Terrestrial influences on the Shiraho fringing reef, Ishigaki Island, Japan: high carbon input relative to phosphate

Measurements of CO₂ system parameters and nutrients showed the potential influence of terrestrial inputs on the carbon budget of a fringing coral reef on Ishigaki Island, Japan. Land-derived freshwaters, including river and ground water, make a relatively large contribution (0.5–1.2% by volume) to the water circulation of the reef. These terrestrial waters exhibit extremely high fugacity of CO₂ (fCO₂ up to 6400 μatm), reflecting enrichments in total alkalinity and dissolved inorganic carbon. Since the dissolved inorganic C:P ratio is anomalously high in terrestrial waters compared with the mean C:P ratios of primary production, excess carbon could be released into the atmosphere. Terrestrial inputs deliver a large quantity of C relative to P. The study site was a source of CO₂ at the time of measurement. Such a situation is likely to prevail all year round, and it may occur elsewhere. Accepted: 20 February 2000     

Predominance of phytoplankton-derived dissolved and particulate organic carbon in a highly eutrophic tropical coastal embayment (Guanabara Bay,Rio de Janeiro,Brazil)

We investigate the carbon dynamics in Guanabara Bay, an eutrophic tropical coastal embayment surrounded by the megacity of Rio de Janeiro (southeast coast of Brazil). Nine sampling campaigns were conducted for dissolved, particulate and total organic carbon (DOC, POC and TOC), dissolved inorganic carbon (DIC), partial pressure of CO₂ (pCO₂), chlorophyll a (Chl a), pheo-pigments and ancillary parameters. Highest DOC, POC and Chl a concentrations were found in confined-shallow regions of the bay during the summer period with strong pCO₂ undersaturation, and DOC reached 82 mg L^?1, POC 152 mg L^?1, and Chl a 800 μg L^?1. Spatially and temporally, POC and DOC concentrations varied positively with total pigments, and negatively with DIC. Strong linear correlations between these parameters indicate that the production of TOC translates to an equivalent uptake in DIC, with 85% of the POC and about 50% of the DOC being of phytoplanktonic origin. Despite the shallow depths of the bay, surface waters were enriched in POC and DOC relative to bottom waters in periods of high thermohaline stratification. The seasonal accumulation of phytoplankton-derived TOC in the surface waters reached about 105 g C m^?2 year^?1, representing between 8 and 40% of the net primary production. The calculated turnover time of organic carbon was 117 and 34 days during winter and summer, respectively. Our results indicate that eutrophication of coastal bays in the tropics can generate large stocks of planktonic biomass and detrital organic carbon which are permanently being produced and partially degraded and buried in sediments.     

Sources and export fluxes of inorganic and organic carbon and nutrient species from the seasonally ice-covered Yukon River

Climate and environmental changes are having profound impacts on Arctic river basins, but the biogeochemical response remains poorly understood. To examine the effect of ice formation on temporal variations in composition and fluxes of carbon and nutrient species, monthly water and particulate samples collected from the lower Yukon River between July 2004 and September 2005 were measured for concentrations of organic and inorganic C, N, and P, dissolved silicate (Si(OH)₄), and stable isotope composition (δD and δ¹⁸O). All organic carbon and nutrient species had the highest concentration during spring freshet and the lowest during the winter season under the ice, indicating dominant sources from snowmelt and flushing of soils in the drainage basin. In contrast, inorganic species such as dissolved inorganic carbon (DIC) and Si(OH)₄ had the highest concentrations in winter and the lowest during spring freshet, suggesting dilution during snowmelt and sources from groundwater and leaching/weathering of mineral layer. The contrasting relation with discharge between organic, such as dissolved organic carbon (DOC), and inorganic, such as DIC and Si(OH)₄, indicates hydrological control of solute concentration but different sources and transport mechanisms for organic and inorganic carbon and nutrient species. Concentration of DOC also shows an inter-annual variability with higher DOC in 2005 (higher stream flow) than 2004 (lower stream flow). Average inorganic N/P molar ratio was 110?±?124, with up to 442 under the ice and 38–70 during the ice-open season. While dissolved organic matter had a higher C/N ratio under the ice (45–62), the particulate C/N ratio was lower during winter (21–26) and spring freshet (19). Apparent fractionation factors of C, N, P, Si and δD and δ¹⁸O between ice and river water varied considerably, with high values for inorganic species such as DIC and Si(OH)₄ (45 and 9550, respectively) but lower values for DOC (4.7). River ice formation may result in fractionation of inorganic and organic solutes and the repartitioning of seasonal flux of carbon and nutrient species. Annual export flux from the Yukon River basin was 1.6?×?10¹² g-DOC, 4.4?×?10¹² g-DIC, and 0.89?×?10¹² g-POC during 2004–2005. Flux estimation without spring freshet sampling results in considerable underestimation for organic species but significant overestimation for inorganic species regardless of the flux estimation methods used. Without time-series sampling that includes frozen season, an over- or under-estimation in carbon and nutrient fluxes will occur depending on chemical species. Large differences in carbon export fluxes between studies and sampling years indicate that intensive sampling together with long-term observations are needed to determine the response of the Yukon River to a changing climate.     

Effect of catchment characteristics on aquatic carbon export from a boreal catchment and its importance in regional carbon cycling

Inland waters transport and emit into the atmosphere large amounts of carbon (C), which originates from terrestrial ecosystems. The effect of land cover and land‐use practises on C export from terrestrial ecosystems to inland waters is not fully understood, especially in heterogeneous landscapes under human influence. We sampled for dissolved C species in five tributaries with well‐determined subcatchments (total size 174.5 km²), as well as in various points of two of the subcatchments draining to a boreal lake in southern Finland over a full year. Our aim was to find out how land cover and land‐use affect C export from the catchments, as well as CH₄ and CO₂ concentrations of the streams, and if the origin of C in stream water can be determined from proxies for quality of dissolved organic matter (DOM). We further estimated the gas evasion from stream surfaces and the role of aquatic fluxes in regional C cycling. The export rate of C from the terrestrial system through an aquatic conduit was 19.3 g C m^?2(catchment) yr^?1, which corresponds to 19% of the estimated terrestrial net ecosystem exchange of the catchment. Most of the C load to the recipient lake consisted of dissolved organic carbon (DOC, 6.1 ± 1.0 g C m^?2 yr^?1); the share of dissolved inorganic carbon (DIC) was much smaller (1.0 ± 0.2 g C m^?2 yr^?1). CO₂ and CH₄ emissions from stream and ditch surfaces were 7.0 ± 2.4 g C m^?2 yr^?1 and 0.1 ± 0.04 g C m^?2 yr^?1, respectively, C emissions being thus equal with C load to the lake. The proportion of peatland in the catchment and the drainage density of peatland increased DOC in streams, whereas the proportion of agricultural land in the catchment decreased it. The opposite was true for DIC. Drained peatlands were an important CH₄ source for streams.     

A stable carbon isotope study of dissolved inorganic carbon cycling in a softwater lake

The dissolved inorganic carbon (DIC) cycle in a softwater lake was studied using natural variations of the stable isotopes of carbon,¹²C and¹³C. During summer stratification there was a progressive decrease in epilimnion DIC concentration with a concomitant increase in ¹³C_DIC), due to preferential uptake of¹²C by phytoplankton and a change in the dominant CO₂ source from inflow andin situ oxidation to invasion from the atmosphere. There was an increase in hypolimnion DIC concentration throughout summer with a concomitant general decrease in ¹³C_DIC from oxidation of the isotopically light particulate organic carbon that sank down through the thermocline from the epilimnion.Mass balance calculations of DI¹²C and DI¹³C in the epilimnion for the summer (June 23–September 25) yield a mean rate of net conversion of DIC to organic carbon (C_org) of 430 ± 150 moles d^-1 (6.5 ± 1.8 m moles m^-2 d^-1. Net CO₂ invasion from the atmosphere was 420 ± 120 moles d^-1 (6.2 ± 1.8 m moles m^-2 d^-1) with an exchange coefficient of 0.6 ± 0.3m d^-1. These results imply that at least for the summer months the phytoplankton obtained about 90% of their carbon from atmosphere CO₂. About 50% of CO₂ invasion and conversion to C_org for the summer occurred during a two week interval in mid-summer.DIC concentration increased in the hypolimnion at a rate of 350 ± 70 moles DIC d^-1 during summer stratification. The amount of DIC added to the hypolimnion was equivalent to 75 ± 20% of net conversion of DIC to C_org in the euphotic zone over spring and summer implying rapid degradation of POC in the hypolimnion. The ¹³C of DIC added to the deep water (-22.) was too heavy to have been derived from oxidation of particulate organic carbon alone. About 20% of the added DIC must have diffused from hypolimnetic sediments where relatively heavy CO₂ (-7) was produced by a combination of POC oxidation and as a by-product of methanogenesis.     

Modeling the carbon cycle in Lake Matano

Lake Matano, Indonesia, is a stratified anoxic lake with iron‐rich waters that has been used as an analogue for the Archean and early Proterozoic oceans. Past studies of Lake Matano report large amounts of methane production, with as much as 80% of primary production degraded via methanogenesis. Low δ¹³C values of DIC in the lake are difficult to reconcile with this notion, as fractionation during methanogenesis produces isotopically heavy CO₂. To help reconcile these observations, we develop a box model of the carbon cycle in ferruginous Lake Matano, Indonesia, that satisfies the constraints of CH₄ and DIC isotopic profiles, sediment composition, and alkalinity. We estimate methane fluxes smaller than originally proposed, with about 9% of organic carbon export to the deep waters degraded via methanogenesis. In addition, despite the abundance of Fe within the waters, anoxic ferric iron respiration of organic matter degrades <3% of organic carbon export, leaving methanogenesis as the largest contributor to anaerobic organic matter remineralization, while indicating a relatively minor role for iron as an electron acceptor. As the majority of carbon exported is buried in the sediments, we suggest that the role of methane in the Archean and early Proterozoic oceans is less significant than presumed in other studies.     

The carbon flux of global rivers: A re-evaluation of amount and spatial patterns

Global rivers connect three large carbon reservoirs in the world: soil, atmosphere, and ocean. The amount and spatial pattern of riverine carbon flux are essential for the global carbon budget but are still not well understood. Therefore, three linear regression models for riverine DOC (dissolved organic carbon), POC (particulate organic carbon), and DIC (dissolved inorganic carbon) fluxes were established with related generating and transfer factors based on an updated global database. The three models then were applied to simulate the spatial distribution of riverine DOC, POC, and DIC fluxes and to estimate the total global riverine carbon flux. The major conclusions of this study are as follows: the correlation analysis showed that riverine DOC flux is significantly related to discharge (r² = 0.93, n = 109) and soil organic carbon amount (r² = 0.60), POC flux increases with discharge (r² = 0.55, n = 98) and amount of soil erosion (r² = 0.48), and DIC flux is strongly linked to CO₂ consumption by rock weathering (r² = 0.66, n = 111) and discharge (r² = 0.63). In addition, Asia exports more DOC and POC than other continents and North America exports more DIC. The Atlantic Ocean accepts the major portion of riverine DOC, POC, and DIC fluxes of all the oceans. The highest riverine DOC flux occurs in the 0–30°S zone, and the highest riverine POC and DIC fluxes appear in the 30–60°N zone. Furthermore, re-estimation revealed that global rivers export approximately 1.06 Pg C to oceans every year, including 0.24 Pg DOC, 0.24 Pg POC, 0.41 Pg DIC, and 0.17 Pg PIC.     

Particulate organic and dissolved inorganic carbon stable isotopic compositions in Taylor Valley lakes,Antarctica: the effect of legacy

In perennially ice-covered lakes of Taylor Valley, Antarctica, “legacy”, a carryover of past ecosystem events, has primarily been discussed in terms of nutrient and salinity concentrations and its effect on the current ecology of the lakes. In this study, we determine how residual pools of ancient carbon affect the modern carbon abundance and character in the water columns of Lakes Fryxell, Hoare, and Bonney. We measure the stable carbon isotopic compositions and concentrations of particulate organic carbon (POC) and dissolved inorganic carbon (DIC) in the water column of these lakes over four seasons (1999–2002). These data are presented and compared with all the previously published Taylor Valley lacustrine carbon stable isotopic data. Our results show that the carbon concentrations and isotopic compositions of the upper water columns of those lakes are controlled by modern processes, while the lower water columns are controlled to varying degrees by inherited carbon pools. The water column of the west lobe of Lake Bonney is dominated by exceptionally high concentrations of DIC (55,000–75,000 μmol l⁻¹) reflecting the long period of ice-cover on this lake. The east lobe of Lake Bonney has highly enriched δ¹³C_DIC values resulting from paleo-brine evaporation effects in its bottom waters, while its high DIC concentrations provide geochemical evidence that its middle depth waters are derived from West Lake Bonney during a hydrologically connected past. Although ancient carbon is present in both Lake Hoare and Lake Fryxell, the δ¹³C_DIC values in bottom waters suggest dominance by modern primary productivity-related processes. Anaerobic methanogenesis and methanotrophy are also taking place in the lower water column of Lake Fryxell with enough methane, oxidized anaerobically, to contribute to the DIC pool. We also show how stream proximity and high flood years are only a minor influence on the carbon isotopic values of both POC and DIC. The Taylor Valley lake system is remarkably stable in both inter-lake and intra-lake carbon dynamics. Handling editor: K. Martens     

Dissolved carbon in an urban area of a river in the Brazilian Amazon

The main objective of this study was to evaluate dissolved organic and inorganic carbon dynamics along upstream and downstream reaches of the Acre River draining the city of Rio Branco, in the state of Acre, Brazil. Dissolved organic carbon (DOC) concentrations in the Acre River were significantly higher during the wet season, ranging from 385 ± 160 to 430 ± 131 ??M among the stations, with no difference in upstream and downstream concentrations. Dissolved inorganic carbon (DIC) showed an inverse pattern, with higher concentrations in the dry season, ranging from 816 ± 215 to 998 ± 754 ??M among the stations, as well as no difference in upstream and downstream DIC concentrations. Bicarbonate was the dominant DIC fraction and was mainly observed during the dry season. Due to lower pH values during the wet season, CO₂ partial pressure (pCO₂) in the Acre River was higher in the wet season, with values ranging from 4,567 ± 1,813 to 4,893 ± 837 ppm among the stations. Our results indicate that, although the Acre River drains a large city with significant sewage disposal into the river, seasonal hydrological processes are the main driver of dissolved carbon dynamics, even in the downstream study reach directly influenced by urbanization.     

The flux of carbon from rivers: the case for flux from England and Wales

This study uses the extensive monitoring datasets of the Environment Agency of England and Wales to calculate the flux of dissolved organic carbon (DOC); particulate organic carbon (POC); and excess dissolved CO₂ through English and Welsh rivers. The innovation of this study’s approach is to account for the losses of carbon within the fluvial system as well as fluxes at the catchment outlet. In order to make this assessment this study considers: the biochemical oxygen demand (BOD) as a measure of the degradation of DOC; and the dissolved CO₂ concentration of groundwater as calculated and apportioned into surface waters on the basis of Ca concentrations. The study shows that the best estimate of carbon export, via rivers, from England and Wales is 10.34 Mg C/km²/year, with 4.19 Mg C/km²/year of this going to the atmosphere. The mapping of the carbon export shows that there are regional hotspots of carbon export and in a small number of cases rivers could be net sinks of carbon due to their low dissolved CO₂ content relative to the atmosphere. The flux calculated by this approach is probably still an underestimate of the carbon flux through fluvial systems but the scale of the export is greater than that previously reported and there is evidence that the fluvial flux of carbon is increasing on a decadal scale.     

大亚湾春季溶解无机碳的分布特征

于2010年5月对大亚湾溶解无机碳(DIC)进行采样调查,分析了大亚湾溶解无机碳空间分布特征,并讨论了大亚湾溶解无机碳与各环境要素(pH、水温、溶解氧和叶绿素a等)的相关性。大亚湾表层水域的DIC含量在24.26～26.13mg.L-1之间;底层水域的DIC含量在24.06～26.89mg.L-1之间。大亚湾表层水体中DIC含量的高值区集中在大辣甲-桑洲连线以北水域,然后呈现出向四周逐渐递减的分布趋势;底层水体中DIC含量高值区集中于西南部水域(大辣甲南部),总体呈现出由南部向北部逐渐递减的分布趋势。大亚湾DIC与水温和叶绿素a呈现负相关系,与pH、DO和盐度呈现正相关关系,但从相关的显著性来看,DIC与以上各环境因子的相关系数均不高。     

Kohlenstoffpumpen im Ozean steuern das Klima. Globale Erwärmung

Here we describe how microscopic marine algae and animals, the plankton impact global climate and how the changing concentration of the climate relevant gas carbon dioxide (CO₂) result in shifts in the marine carbonate system, including a drop in the pH (ocean acidification). Three processes, summarily called the carbon pumps transfer carbon between the surface and the deep ocean: The solubility pump moves inorganic, dissolved carbon to depth. The biological pump transports organic, particulate carbon downward. The carbonate counter pump describes the formation and sedimentation of carbonate tests, whereby CO₂ is released into the surface ocean. On geological timescales the biological pump was strengthened during glacial times due to an increase in the iron supply, which lead to a (continued) decline in temperatures. Hence, the idea to fertilize the ocean with iron thereby strengthening the biological pump and mediating today's climate change has been discussed for the past 20 years.     

Dissolved carbon leaching from soil is a crucial component of the net ecosystem carbon balance

Estimates of carbon leaching losses from different land use systems are few and their contribution to the net ecosystem carbon balance is uncertain. We investigated leaching of dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), and dissolved methane (CH₄), at forests, grasslands, and croplands across Europe. Biogenic contributions to DIC were estimated by means of its δ¹³C signature. Leaching of biogenic DIC was 8.3±4.9 g m^?2 yr^?1 for forests, 24.1±7.2 g m^?2 yr^?1 for grasslands, and 14.6±4.8 g m^?2 yr^?1 for croplands. DOC leaching equalled 3.5±1.3 g m^?2 yr^?1 for forests, 5.3±2.0 g m^?2 yr^?1 for grasslands, and 4.1±1.3 g m^?2 yr^?1 for croplands. The average flux of total biogenic carbon across land use systems was 19.4±4.0 g C m^?2 yr^?1. Production of DOC in topsoils was positively related to their C/N ratio and DOC retention in subsoils was inversely related to the ratio of organic carbon to iron plus aluminium (hydr)oxides. Partial pressures of CO₂ in soil air and soil pH determined DIC concentrations and fluxes, but soil solutions were often supersaturated with DIC relative to soil air CO₂. Leaching losses of biogenic carbon (DOC plus biogenic DIC) from grasslands equalled 5–98% (median: 22%) of net ecosystem exchange (NEE) plus carbon inputs with fertilization minus carbon removal with harvest. Carbon leaching increased the net losses from cropland soils by 24–105% (median: 25%). For the majority of forest sites, leaching hardly affected actual net ecosystem carbon balances because of the small solubility of CO₂ in acidic forest soil solutions and large NEE. Leaching of CH₄ proved to be insignificant compared with other fluxes of carbon. Overall, our results show that leaching losses are particularly important for the carbon balance of agricultural systems.     

Carbon flux between an estuary and the ocean: a case for outwelling

The classical outwelling hypothesis states that small coastal embayments (e.g. estuaries, wetlands) export their excess production to inshore marine waters. In line with this notion, the present study tested whether the Swartkops estuary acts as source or sink for carbon. To this end, concentrations of dissolved inorganic carbon (DIC), dissolved organic carbon (DOC) and particulate organic carbon (POC) were determined hourly during the first monthly spring and neap tides over one year in the tidal waters entering and leaving the estuary. Each sampling session spanned a full tidal cycle, yielding a total of 936 concentration estimates. Carbon fluxes were calculated by integrating concentrations with water flow rates derived from a hydrodynamic model calibrated for each sampling datum. Over the year, exports to marine waters markedly exceeded imports to the estuary for all carbon species: on the basis of total spring tidal drainage area, 1083 g m^–2 of DIC, 103 g m^–2 of DOC, and 123 g m^–2 of POC left the estuary annually. Total carbon export from the estuary to the ocean amounted to 4755 tonnes, of which 83% was in the inorganic form (DIC). Thus, the bulk of carbon moving in the water column is inorganic - yet, DIC seems to be measured only rarely in most flux studies of this nature. Salt marshes cover extensive areas in this estuary and produce some carbon, particularly DOC, but productivity of the local Spartina species is low (P:B=1.1). Consequently, the bulk of carbon exported from the estuary appears to originate from the highly productive macroinvertebrate and the phytoplankton component and not from the salt marsh plants.