Significance of riverine carbon transport: A case study of a large tropical river, Godavari (India)

Although riverine carbon fluxes are a minor component of the global carbon cycle, thetransfer of organic carbon from land to ocean represents a flux of potential carbon storage, irre-versible over 10~3 to 10~4 a. Future carbon transfers through river basins are expected to accelerate,with respect to both sources and sinks, because of the large-scale human driven land-use and land-cover changes. Thus, the increased amounts of carbon transported to and sequestered inmarine sediments (through fertilization by river-borne inorganic nutrients) may be an important netsink for anthropogenic CO_2. Particularly, the humid tropics of South Asia are regions very sensitiveto this lateral C transport because of high precipitation and high rates of land use and cover change. In this paper we report on the role of upland tributaries in the transport processes influ-encing the lateral carbon and nitrogen fluxes of the Godavari, a large tropical river of India. By far,dissolved inorganic carbon (DIC) is the dominant form of carbon transport in the river basin. It con-stitutes as much as 75% to the total carbon load. Particulate and dissolved organic carbon (POC and DOC) fluxes account for 21% and 4%, respectively. In the upper basin, DOC fluxes exceedthat of POC due to large-scale anthropogenic activities. In contrast, tributaries in the central basinare characterized by comparable fluxes of POC and DOC. However, downriver POC export is 35%less than the import from upriver and tributaries due to the entrainment of sediments in river channels and dam sites. We argue that for highly disturbed watersheds in tropical regions, down-stream transport of sediments and carbon requires long-term sampling programmes.     

Shifts in the carbon dynamics in a tropical lowland river system (Tana River,Kenya) during flooded and non-flooded conditions

Rivers transport sediment and carbon (C) from the continents to the ocean, whereby the magnitude and timing of these fluxes depend on the hydrological regime. We studied the sediment and carbon dynamics of a tropical river system at two sites along the lower Tana River (Kenya), separated by a 385 km stretch characterized by extensive floodplains, to understand how the river regime affects within-river C processing as well as the C exchange between floodplain and river. Sampling took place during three different wet seasons (2012–2014), with extensive flooding during one of the campaigns. We measured the suspended sediment concentration, the concentration and stable isotope signature of three different carbon species (particulate and dissolved organic carbon, POC and DOC, and dissolved inorganic carbon, DIC) and other auxiliary parameters. During non-flooded conditions, the total C flux was dominated by POC (57–72%) and there was a downstream decrease of the total C flux. DIC was dominating during the flooded season (56–67%) and the flux of DIC and DOC coming from the inundated floodplains resulted in a downstream increase of the total carbon flux. Our data allowed us to construct a conceptual framework for the C dynamics in river systems, whereby nine major fluxes were identified. The application of this framework highlighted the dominance of POC during non-flooded conditions and the significant CO₂ emissions during the flooded season. Furthermore, it identified the exchange of POC with the floodplain as an important factor to close the C budget of the river.     

Variability and transport of suspended sediment,particulate and dissolved organic carbon in the tidal freshwater Hudson River

Measurements of suspended matter, particulate organic carbon and dissolved organic carbon were made over a three year period at stations spanning 150 km of the tidal freshwater Hudson River. Suspended matter concentrations varied from year-to-year and were not related to freshwater discharge. The increase in suspended matter with depth in vertical profiles suggests that, during medium to low flow conditions, resuspension of bottom sediments was as important a source of sediment as loadings from tributaries. Particulate organic carbon showed significant variability among stations, and both autochthonous primary production and detrital organic matter are contributing to POC standing stocks. Dissolved organic carbon represented over half of the total organic carbon in the water column and showed little variation among stations.Examining downstream changes in transport showed that there was significant production of both suspended matter and POC within the study reach during the ice-free season. Tributary loadings within the study reach do not appear to be the cause of these increases in downstream transport. Dissolved organic carbon behaved conservatively in that there was no evidence for net production or net consumption within the river.The spatial/temporal patterns and analyses of transport suggest that suspended matter and POC, but not DOC, were controlled to a significant extent by processes occurring within the river and were not simply related to loadings from outside.     

Fluxes of dissolved and nonfossil particulate organic carbon from an Oceania small river (Lanyang Hsi) in Taiwan

Concentrations of dissolved and particulate organic carbon (DOC & POC) in river waters were measuredduring 1993–1994 in the Lanyang Hsi watershed, which representsa typical small Oceania river. The DOC concentrations varied in the range of 0.5–4 mg/l during non-typhoon period, but rose to as highas 8 mg/l during Typhoon Tim in July, 1994. Based on the log-linearrelationship between the DOC load and the discharge rate, weestimated the DOC export to be 3.4 ± 0.6 ktC/yr,and the DOC yield to be 4.1 ± 0.7 gC/m²/yr,which is considerably higher than a former estimate (ca.0.1 gC/m²/yr) for the Oceania. On the other hand, the DOC yield is less than the concurrent POC yield (21.7 ± 4.7gC/m²/yr) by a factor of five, but most of theexported POC is fossil carbon. Under the assumption that the suspended sediments contain a mean fossil POC content of0.5%, the nonfossil POC yield was calculated to be 4.6± 3.0 gC/m²/yr, comparable to theDOC yield. Since DOC and nonfossil POC are directly related to theecosystem, their combined fluxes give a biogenic organic carbonyield of 8.7 ± 3.1 gC/m²/yr.     

Seasonal and spatial distribution of dissolved and particulate organic carbon and bacteria in the bank of an impounding reservoir on the Enns River, Austria

1. Interstitial bacterial abundance, production and ectoenzyme activity were investigated over an annual cycle in an Austrian river when infiltration of oligotrophic river water into a river-bank was artificially enhanced. These microbial parameters were related to porewater chemistry and the concentration of particulate (POC) and dissolved organic carbon (DOC).
2. Porewater chemistry reflected the hydrodynamic mixing of infiltrating river water with riparian groundwater. Seasonal fluctuations in the microbial parameters resulted mainly from changes in temperature and organic matter supply. Seasonal change in porewater chemistry in the river-bank was detectable laterally only within the first metre of the sediment and decreased rapidly with increasing distance from the sediment–water interface.
3. The DOC concentration decreased only slightly during lateral transport through the aquifer, while total organic carbon (TOC) concentration as well as abundance and activity of interstitial bacteria were reduced by up to one order of magnitude within the top metre of the sediment. Retention of incoming particulate matter structured the lateral distribution pattern of TOC concentration. The POC and not the DOC pool was the main source of carbon for interstitial bacteria and, therefore, the quality of POC determines the distribution of microbial metabolism within the riparian zone.     

Organic carbon transport and C/N ratio variations in a large tropical river: Godavari as a case study,India

This study gives an insight into the source of organic carbon and nitrogen in the Godavari river and its tributaries, the yield of organic carbon from the catchment, seasonal variability in their concentration and the ultimate flux of organic and inorganic carbon into the Bay of Bengal. Particulate organic carbon/particulate organic nitrogen (POC/PON or C/N) ratios revealed that the dominant source of organic matter in the high season is from the soil (C/N = 8–14), while in the rest of the seasons, the river-derived (in situ) phytoplankton is the major source (C/N = l–8). Amount of organic materials carried from the lower catchment and flood plains to the oceans during the high season are 3 to 91 times higher than in the moderate and low seasons. Large-scale erosion and deforestation in the catchment has led to higher net yield of organic carbon in the Godavari catchment when compared to other major world rivers. The total flux of POC, and dissolved inorganic carbon (DIC) from the Godavari river to the Bay of Bengal is estimated as 756 × 10⁹ and 2520 × 10⁹ g yr^–1, respectively. About 22% of POC is lost in the main channel because of oxidation of labile organic matter, entrapment of organic material behind dams/sedimentation along flood plains and river channel; the DIC fluxes as a function of alkalinity are conservative throughout the river channel. Finally, the C/N ratios (12) of the ultimate fluxes of particulate organic carbon suggest the dominance of refractory/stable soil organic matter that could eventually get buried in the coastal sediments on a geological time scale.     

Dial organic carbon fluctuations in a mangrove tidal creek in Sepetiba bay, Southeast Brazil

The carbon (C) concentration and flux, as dissolved organic carbon (DOC), particulate organic carbon (POC) and macrodetritus (MD), were quantified through 4 tidal cycles in a mangrove tidal creek in Southeastern Brazil. DOC was the major fraction of the total C concentration, accounting for 68 and 61% of the total C concentration during ebb and flood periods respectively. Concentrations of DOC (Ebb = 3.41 +/- 0.57 mgC.L-1 and Flood = 3.55 +/- 0.76 mgC.L-1) and POC (Ebb = 1.73 +/- 0.99 mgC.L-1 and Flood = 1.28 +/- 0.45 mgC.L-1) were relatively similar during the four tidal cycles. Macrodetritus presented a wide variation with concentration peaks probably related to external forces, such as winds, which enrich the ebb flow with leaf litter. DOC and POC fluxes depended primarily on tidal and net water fluxes, whereas MD fluxes were not. The magnitude of the DOC and POC fluxes varied with the area flooded at high tide, but not the MD fluxes. DOC was the major form of carbon export to Sepetiba Bay. During the four tidal cycles, the forest exported a total of 1.2 kg of organic carbon per ha, mostly as DOC (60%), followed by POC (22%) and MD (18%).     

Particulate organic matter quality influences nitrate retention and denitrification in stream sediments: evidence from a carbon burial experiment

Organic carbon supply is linked to nitrogen transformation in ecosystems. However, the role of organic carbon quality in nitrogen processing is not as well understood. We determined how the quality of particulate organic carbon (POC) influenced nitrogen transformation in stream sediments by burying identical quantities of varying quality POC (northern red oak (Quercus rubra) leaves, red maple (Acer rubrum) leaves, red maple wood) in stream mesocosms and measuring the effects on nitrogen retention and denitrification compared to a control of combusted sand. We also determined how POC quality affected the quantity and quality of dissolved organic carbon (DOC) and dissolved oxygen concentration in groundwater. Nitrate and total dissolved nitrogen (TDN) retention were assessed by comparing solute concentrations and fluxes along groundwater flow paths in the mesocosms. Denitrification was measured by in situ changes in N₂ concentrations (using MIMS) and by acetylene block incubations. POC quality was measured by C:N and lignin:N ratios and DOC quality was assessed by fluorescence excitation emission matrix spectroscopy. POC quality had strong effects on nitrogen processing. Leaf treatments had much higher nitrate retention, TDN retention and denitrification rates than the wood and control treatments and red maple leaf burial resulted in higher nitrate and TDN retention rates than burial of red oak leaves. Leaf, but not wood, burial drove pore water to severe hypoxia and leaf treatments had higher DOC production and different DOC chemical composition than the wood and control treatments. We think that POC quality affected nitrogen processing in the sediments by influencing the quantity and quality of DOC and redox conditions. Our results suggest that the type of organic carbon inputs can affect the rates of nitrogen transformation in stream ecosystems.     

Carbon isotope biogeochemistry of tropical small mountainous river, estuarine, and coastal systems of Puerto Rico

Recent studies have shown that small mountainous rivers (SMRs) may act as sources of aged and/or refractory carbon (C) to the coastal ocean, which may increase organic C burial at sea and subsidize coastal food webs and heterotrophy. However, the characteristics and spatial and temporal variability of C and organic matter (OM) exported from tropical SMR systems remain poorly constrained. To address this, the abundance and isotopic character (δ¹³C and Δ¹⁴C) of the three major C pools were measured in two Puerto Rico SMRs with catchments dominated by different land uses (agricultural vs. non-agricultural recovering forest). The abundance and character of C pools in associated estuaries and adjacent coastal waters were also examined. Riverine dissolved and particulate organic C (DOC and POC, respectively) concentrations were highly variable with respect to land use and sampling month, while dissolved inorganic C (DIC) was significantly higher at all times in the agricultural catchment. In both systems, riverine DOC and POC ranged from modern to highly aged (2,340 years before present), while DIC was always modern. The agricultural river and irrigation canals contained very old DOC (1,184 and 2,340 years before present, respectively), which is consistent with findings in temperate SMRs and indicates that these tropical SMRs provide a source of aged DOC to the ocean. During months of high river discharge, OM in estuarine and coastal waters had C isotope signatures reflective of direct terrestrial input, indicating that relatively unaltered OM is transported to the coastal ocean at these times. This is also consistent with findings in temperate SMRs and indicates that C transported to the coastal ocean by SMRs may differ from that of larger rivers because it is exported from smaller catchments that have steeper terrains and fewer land-use types.     

How organic carbon derived from multiple sources contributes to carbon sequestration processes in a shallow coastal system?

Carbon captured by marine organisms helps sequester atmospheric CO₂, especially in shallow coastal ecosystems, where rates of primary production and burial of organic carbon (OC) from multiple sources are high. However, linkages between the dynamics of OC derived from multiple sources and carbon sequestration are poorly understood. We investigated the origin (terrestrial, phytobenthos derived, and phytoplankton derived) of particulate OC (POC) and dissolved OC (DOC) in the water column and sedimentary OC using elemental, isotopic, and optical signatures in Furen Lagoon, Japan. Based on these data analysis, we explored how OC from multiple sources contributes to sequestration via storage in sediments, water column sequestration, and air–sea CO₂ exchanges, and analyzed how the contributions vary with salinity in a shallow seagrass meadow as well. The relative contribution of terrestrial POC in the water column decreased with increasing salinity, whereas autochthonous POC increased in the salinity range 10–30. Phytoplankton‐derived POC dominated the water column POC (65–95%) within this salinity range; however, it was minor in the sediments (3–29%). In contrast, terrestrial and phytobenthos‐derived POC were relatively minor contributors in the water column but were major contributors in the sediments (49–78% and 19–36%, respectively), indicating that terrestrial and phytobenthos‐derived POC were selectively stored in the sediments. Autochthonous DOC, part of which can contribute to long‐term carbon sequestration in the water column, accounted for >25% of the total water column DOC pool in the salinity range 15–30. Autochthonous OC production decreased the concentration of dissolved inorganic carbon in the water column and thereby contributed to atmospheric CO₂ uptake, except in the low‐salinity zone. Our results indicate that shallow coastal ecosystems function not only as transition zones between land and ocean but also as carbon sequestration filters. They function at different timescales, depending on the salinity, and OC sources.     

Downstream alteration of the composition and biodegradability of particulate organic carbon in a mountainous,mixed land-use watershed

Despite increasing recognition of storm-induced organic carbon (C) export as a significant loss from the terrestrial C balance, little is known about the biodegradation and chemical transformation of particulate organic carbon (POC) in mountainous river systems. We combined analyses of C isotopes, solution-state ¹H NMR, and lipid biomarkers with biodegradable dissolved organic C (BDOC) measurements to investigate downstream changes of POC composition and biodegradability at a mountainous, mixed land-use watershed in South Korea. Water and suspended sediment (SS) samples were collected in a forested headwater stream, a downstream agricultural stream, and two downstream rivers during peak flow periods of four storm events, using either sequential grab sampling from the headwater stream to the most downstream river within a few hours around the peak flow or sediment samplers deployed during the whole storm event. DOC concentrations exhibited relatively small changes across sites, whereas POC concentrations were highest in the agricultural stream, and tapered along downstream reaches. The δ¹³C and δ¹⁵N of SS in the agricultural stream were distinct from up- and downstream signatures and similar to those for erosion source soils and lake bottom sediment, although increases in radiocarbon age indicated continuous compositional changes toward the lake. ¹H NMR spectra of SS and deposited sediment exhibited downstream decreases in carbohydrates and lignin but enrichment of organic structures related to microbial proteins and plant wax. The downstream sediments had more microbial n-alkanes and lipid markers indicating anthropogenic origin such as coprostanol compared to the forest soil n-alkanes dominated by plant wax. While the BDOC concentrations of filtered waters differed little between sites, the BDOC concentrations and protein- to humic-like fluorescence ratios of DOC leached from SS during a 13-day incubation were higher in downstream rivers, pointing to contribution of labile POC components to the enhanced biodegradation. Overall, inputs of microbial and anthropogenic origin, in interplay with deposition and mineralization, appear to substantially alter POC composition and biodegradability during downstream transport, raising a question on the conventional view of mountainous river systems as a passive conduit of storm pulses of POC.     

森林生态系统可溶性碳和颗粒碳通量

可溶性碳(Dissolved carbon,DC)和颗粒碳(particulate carbon,PC)通量作为森林生态系统碳收支的重要组分,在森林固碳功能的评价和模型预测中具有重要意义,但常因认识不足、测定困难等而在森林碳汇研究中被忽略。综述了森林生态系统DC和PC的组成、作用、相关生态过程及其影响因子,并展望了该领域应该优先考虑的研究问题。森林生态系统DC和PC主要包括可溶性有机碳、可溶性无机碳和颗粒有机碳,主要来源于生态系统的净初级生产量。DC和PC是森林土壤的活性碳库,主要以大气沉降、穿透雨和凋落物的形式输入森林土壤系统,并通过土壤呼吸、侧向运输及渗透流失的方式输出生态系统。从局域尺度看,DC和PC通量受根系分泌、细根分解、微生物周转等生物过程的影响较大;从区域尺度看,它们受土壤和植被特性、生态过程耦联关系、气候因子以及全球变化的综合影响。该领域应该优先考虑:(1)探索不同时空尺度下森林生态系统DC和PC通量的控制因子及其耦联关系,揭示其中的驱动机理;(2)探索DC和PC与其它森林生态系统碳组分的相互关系及转化,阐明DC和PC通量与其它养分之间潜在的生态化学计量关系;(3)探索全球变化,特别是人类活动(如森林经营)和极端干扰事件(如林火、旱涝、冰冻、冻融交替等)对森林生态系统DC和PC通量的影响。     

Natural pipes in blanket peatlands: major point sources for the release of carbon to the aquatic system

Natural soil pipes, which have been widely reported in peatlands, have been shown to contribute significantly to total stream flow. Here, using measurements from eight pipe outlets, we consider the role of natural pipes in the transport of fluvial carbon within a 17.4‐ha blanket‐peat‐covered catchment. Concentrations of dissolved and particulate organic carbon (DOC and POC) from pipe waters varied greatly between pipes and over time, ranging between 5.3 and 180.6 mg L^?1 for DOC and 0.08 and 220 mg L^?1 for POC. Pipes were important pathways for peatland fluvial carbon export, with fluxes varying between 0.6 and 67.8 kg yr^?1 (DOC) and 0.1 and 14.4 kg yr^?1 (POC) for individual pipes. Pipe DOC flux was equivalent to 20% of the annual DOC flux from the stream outlet while the POC flux from pipes was equivalent to 56% of the annual stream POC flux. The proportion of different forms of aquatic carbon to total aquatic carbon flux varied between pipes, with DOC ranging between 80.0% and 91.2%, POC from 3.6% to 17.1%, dissolved CO₂‐C from 2.4% to 11.1% and dissolved CH₄‐C from 0.004% to 1.3%. The total flux of dissolved CO₂‐C and CH₄‐C scaled up to all pipe outlets in the study catchment was estimated to be 89.4 and 3.6 kg yr^?1 respectively. Overall, pipe outlets produced discharge equivalent to 14% of the discharge in the stream but delivered an amount of aquatic carbon equivalent to 22% of the aquatic carbon flux at the catchment outlet. Pipe densities in blanket peatlands are known to increase when peat is affected by drainage or drying. Hence, environmental change in many peatlands may lead to an increase in aquatic carbon fluxes from natural pipes, thereby influencing the peatland carbon balance and downstream ecological processes.     

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.     

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.     

Biogeochemical properties of a tropical swamp forest ecosystem in southern Thailand

The distributions of organic matter in the tropical swamps in southern Thailand are reported. The concentrations of particulate and dissolved organic carbon (POC and DOC) in the Bang Nara River, which drains swamp forests and nearby paddy fields, were 2.9 ± 2.0 and 6.2 ± 1.3 mg C l⁻¹, respectively. Although the variation was large, DOC concentration in the Bang Nara River seemed to be higher than POC in November 1992 (DOC/POC ratio, 2.8 ± 2.2). River waters from the upland areas were characterized by low POC and DOC concentrations as compared with Bang Nara River water. The δ¹³C values of POC and river sediments were useful to distinguish between organic matter originating in upland and swamp areas. It is suggested that the distributions of organic matter and its isotopic composition reflect the difference in drainage characteristics between lowland swamp and upland areas. Isotopic analyses of plant leaves and soils revealed that the swamp forest ecosystems were characterized by low δ¹³C and low δ¹⁵N values, which suggested low efficiency of water use by plants and large contributions of atmospheric deposition of nitrogen, respectively. Although CO₂ recycling in the forest might be an important factor determining the δ¹³C values of understory plants, the main process in carbon metabolism of tropical swamp forests would be CO₂ exchange between the atmosphere and forest canopy. Received: May 1, 2001 / Accepted: September 28, 2001     

Dynamic carbon budget of a large shallow lake assessed by a mass balance approach

To study the role of large and shallow hemiboreal lakes in carbon processing, we calculated a 3-year carbon mass balance for Lake Võrtsjärv (Estonia) based on in situ measurements. This balance took into account hydrological and biogeochemical processes affecting dissolved inorganic (DIC), dissolved organic (DOC) and particulate organic (POC) carbon species. Accumulation varied greatly on a seasonal and yearly basis. The lake exported carbon during most of the year except during spring floods and in late autumn. In-lake processes were responsible for exporting POC and storing DOC while DIC switched between storage and export. The carbon cycle was alternatively dominated in 2009 by biogeochemical processes and in 2011 by riverine fluxes, whereas in 2010 the two process types were of the same magnitude. These results suggest that the role of large shallow lakes like Võrtsjärv in the global C cycle is equally driven by hydrological factors, in particular seasonal water level changes, and by biogeochemical in-lake reactions.     

Fluxes of bacteria and organic matter into a blackwater river from river sediments and floodplain soils

1. The Ogeechee River, in south-eastern Georgia, U.S.A, is a blackwater river with an extensive floodplain that is inundated regularly during winter months. Previous studies have shown that low to moderate bacterial production rates cannot support the relatively high suspended bacteria concentrations observed (10^7?-10⁸ cells ml^?1), suggesting an allochthonous source of bacteria. We report the results of a combination of field and flume experiments which demonstrate that river sediments and floodplain soils are significant sources of suspended bacteria during seasonal flooding. Benthic bacteria are also entrained by normal discharges. There are sizeable fluxes of POC and DOC from river sediments and floodplain soils. 2. Bacterial, POC and DOC fluxes (14, 250, and 790 mg Cm^?2 h^?1, respectively) were substantial when water was percolated upward through floodplain soils. 3. Simulation of overland flow using a flume demonstrated further fluxes of bacteria and POC from floodplain soils (up to 61 and 10700 mg Cm^?2h^?1, respectively) and river sediments, but did not yield additional DOC from floodplain soils. 4. These laboratory results are supported by experiments in which we measured significant increases in concentrations of bacteria and DOC in a downstream direction in (i) the main river channel during a winter flood in 1986, and (ii) a floodplain slough (channel side-arm) which re-entered the main channel 800m from its initial divergence. Inputs of bacteria and DOC from the surrounding floodplain were estimated to be up to 3500 kg DOC h^?1, and 4000 kg bacteria Ch^?1 over a 50-km reach. 5. These previously unmeasured fluxes of organic carbon help to explain the high concentrations of suspended bacteria in the Ogeechee River.     

Soil Organic Carbon Redistribution by Water Erosion – The Role of CO2 Emissions for the Carbon Budget

A better process understanding of how water erosion influences the redistribution of soil organic carbon (SOC) is sorely needed to unravel the role of soil erosion for the carbon (C) budget from local to global scales. The main objective of this study was to determine SOC redistribution and the complete C budget of a loess soil affected by water erosion. We measured fluxes of SOC, dissolved organic C (DOC) and CO₂ in a pseudo-replicated rainfall-simulation experiment. We characterized different C fractions in soils and redistributed sediments using density fractionation and determined C enrichment ratios (CER) in the transported sediments. Erosion, transport and subsequent deposition resulted in significantly higher CER of the sediments exported ranging between 1.3 and 4.0. In the exported sediments, C contents (mg per g soil) of particulate organic C (POC, C not bound to soil minerals) and mineral-associated organic C (MOC) were both significantly higher than those of non-eroded soils indicating that water erosion resulted in losses of C-enriched material both in forms of POC and MOC. The averaged SOC fluxes as particles (4.7 g C m⁻² yr⁻¹) were 18 times larger than DOC fluxes. Cumulative emission of soil CO₂ slightly decreased at the erosion zone while increased by 56% and 27% at the transport and depositional zone, respectively, in comparison to non-eroded soil. Overall, CO₂ emission is the predominant form of C loss contributing to about 90.5% of total erosion-induced C losses in our 4-month experiment, which were equal to 18 g C m⁻². Nevertheless, only 1.5% of the total redistributed C was mineralized to CO₂ indicating a large stabilization after deposition. Our study also underlines the importance of C losses by particles and as DOC for understanding the effects of water erosion on the C balance at the interface of terrestrial and aquatic ecosystems.     

Organic carbon transfers in the subtropical Red River system (Viet Nam): insights on CO<Subscript>2</Subscript> sources and sinks

The Red River, draining a 169,000 km² watershed, is the second largest river in Viet Nam and constitutes the main source of water for a large percentage of the population of North Viet Nam. Here we present the results of an investigation into the spatial distribution and temporal dynamics of particulate and dissolved organic carbon (POC and DOC, respectively) in the Red River Basin. POC concentrations ranged from 0.24 to 5.80 mg C L^?1 and DOC concentrations ranged from 0.26 to 5.39 mg C L^?1. The application of the Seneque/Riverstrahler model to monthly POC and DOC measurements showed that, in general, the model simulations of the temporal variations and spatial distribution of organic carbon (OC) concentration followed the observed trends. They also show the impact of high population densities (up to 994 inhab km^?2 in the delta area) on OC inputs in surface runoff from the different land use classes and from urban point sources. A budget of the main fluxes of OC in the whole river network, including diffuse inputs from soil leaching and runoff and point sources from urban centers, as well as algal net primary production and heterotrophic respiration was established using the model results. It shows the predominantly heterotrophic character of the river system and provides an estimate of CO₂ emissions from the river of 330 Gg C year^?1. This value is in reasonable agreement with the few available direct measurements of CO₂ fluxes in the downstream part of the river network.