Transfer of carbon dioxide and methane through the soil‐water‐atmosphere system at Mer Bleue peatland,Canada

Surface waters associated with peatlands, supersaturated with CO₂ and CH₄ with respect to the atmosphere, act as important pathways linking a large and potentially unstable global repository of C to the atmosphere. Understanding the drivers and mechanisms which control C release from peatland systems to the atmosphere will contribute to better management and modelling of terrestrial C pools. We used non‐dispersive infra‐red (NDIR) CO₂ sensors to continuously measure gas concentrations in a beaver pond at Mer Bleue peatland (Canada); measurements were made between July and August 2007. Concentrations of CO₂ in the surface water (10 cm) reached 13 mg C l^?1 (epCO₂ 72), and 26 mg C l^?1 (epCO₂ 133) at depth (60 cm). The study also showed large diurnal fluctuations in dissolved CO₂ which ranged in amplitude from ～1·6 mg C l^?1 at 10 cm to ～0·2 mg C l^?1 at 60 cm depth. CH₄ concentration and supersaturation (epCH₄) measured using headspace analysis averaged 1·47 mg C l^?1 and 3252, respectively; diurnal cycling was also evident in CH₄ concentrations. Mean estimated evasion rates of CO₂ and CH₄ over the summer period were 44·92 ± 7·86 and 0·44 ± 0·25 µg C m^?2s^?1, respectively. Open water at Mer Bleue is a significant summer hotspot for greenhouse gas emissions within the catchment. Our results suggest that CO₂ concentrations during the summer in beaver ponds at Mer Bleue are strongly influenced by biological processes within the water column involving aquatic plants and algae (in situ photosynthesis and respiration). In terms of carbon cycling, soil‐stream connectivity at this time of year is therefore relatively weak. Copyright © 2008 John Wiley & Sons, Ltd.     

A Preliminary Study of Chromophoric Dissolved Organic Matter (CDOM) in Lake Taihu,a Shallow Subtropical Lake in China

The optical properties and spatial distribution of chromophoric dissolved organic matter (CDOM) in Meiliang Bay of Lake Taihu were evaluated and compared to the results in literature. Concentrations of dissolved organic carbon (DOC) ranged from 8.75 to 20.19 mg L^?1 with an average of (13.10 ± 3.51) mg L^?1. CDOM absorption coefficients a(λ) at 280 nm, 355 nm, and 440 nm were in the range 11.28...33.46 m^?1 (average (20.95 ± 5.52) m^?1), 2.42...7.90 m^?1 (average (4.92 ± 1.29) m^?1), and 0.65...2.44 m^?1 (average (1.46 ± 0.44) m^?1), respectively. In general, CDOM absorption coefficient and DOC concentration were found to decrease away from the river inflow to Meiliang Bay towards the lake center. The values of the DOC‐specific absorption coefficients a*(λ), given as absorption coefficient related to mass concentration of organic carbon (C) ranged from 0.28 to 0.47 L mg^?1 m^?1 at 355 nm. The determination coefficients between CDOM absorption and DOC concentration decreased with the increase of wavelength from 280 to 550 nm. The linear regression relationship between CDOM absorption at 280 nm and DOC concentration was following: a(280 nm) = 1.507 L mg^?1 m^?1 · DOC + 1.215 m^?1. The spectral slope S values were dependent on the wavelength range used in the regression. The estimated S values decreased with increasing wavelength range used. A significant negative linear relationship was found between CDOM absorption coefficients, DOC‐specific absorption coefficients and estimated S values especially in longer wavelength range. The linear regression relationship between DOC‐specific absorption coefficients at 440 nm and estimated S values during the wavelength range from 280 to 500 nm was following: a*(440 nm) = (–0.021 μm · S + 0.424) L mg^?1 m^?1.     

Seasonal controls on DOC dynamics in nested upland catchments in NE Scotland

Spatial and temporal variability of hydrological responses affecting surface water dissolved organic carbon (DOC) concentrations are important for determining upscaling patterns of DOC export within larger catchments. Annual and intra‐annual variations in DOC concentrations and fluxes were assessed over 2 years at 12 sites (3·40–1837 km²) within the River Dee basin in NE Scotland. Mean annual DOC fluxes, primarily correlated with catchment soil coverage, ranged from 3·41 to 9·48 g m^?2 yr^?1. Periods of seasonal (summer–autumn and winter–spring) DOC concentrations (production) were delineated and related to discharge. Although antecedent temperature mainly determined the timing of switchover between periods of high DOC in the summer‐autumn and low DOC in winter‐spring, inter‐annual variability of export within the same season was largely dependent on its associated water flux. DOC fluxes ranged from 1·39 to 4·80 g m^?2 season^?1 during summer–autumn and 1·43 to 4·15 g m^?2 season^?1 in winter–spring.Relationships between DOC areal fluxes and catchment scale indicated that mainstem fluxes reflect the averaging of highly heterogeneous inputs from contrasting headwater catchments, leading to convergent DOC fluxes at catchment sizes of ca 100 km². However, during summer–autumn periods, in contrast to winter–spring, longitudinal mainstem DOC fluxes continue to decrease, most likely because of increasing biological processes. This highlights the importance of considering seasonal as well as annual changes in DOC fluxes with catchment scale. This study increases our understanding of the temporal variability of DOC upscaling patterns reflecting cumulative changes across different catchment scales and aids modelling of carbon budgets at different stages of riverine systems. Copyright © 2010 John Wiley & Sons, Ltd.     

Assessing DOC export from a Sphagnum‐dominated peatland using δ13C and δ18O–H2O stable isotopes

Dissolved organic carbon (DOC) originating in peatlands can be mineralized to carbon dioxide (CO₂) and methane (CH₄), two potent greenhouse gases. Knowledge of the dynamics of DOC export via run‐off is needed for a more robust quantification of C cycling in peatland ecosystems, a prerequisite for realistic predictions of future climate change. We studied dispersion pathways of DOC in a mountain‐top peat bog in the Czech Republic (Central Europe), using a dual isotope approach. Although δ¹³C_DOC values made it possible to link exported DOC with its within‐bog source, δ¹⁸O_H2O values of precipitation and run‐off helped to understand run‐off generation. Our 2‐year DOC–H₂O isotope monitoring was complemented by a laboratory peat incubation study generating an experimental time series of δ¹³C_DOC values. DOC concentrations in run‐off during high‐flow periods were 20–30 mg L^?1. The top 2 cm of the peat profile, composed of decaying green moss, contained isotopically lighter C than deeper peat, and this isotopically light C was present in run‐off in high‐flow periods. In contrast, baseflow contained only 2–10 mg DOC L^?1, and its more variable C isotope composition intermittently fingerprinted deeper peat. DOC in run‐off occasionally contained isotopically extremely light C whose source in solid peat substrate was not identified. Pre‐event water made up on average 60% of the water run‐off flux, whereas direct precipitation contributed 40%. Run‐off response to precipitation was relatively fast. A highly leached horizon was identified in shallow catotelm. This peat layer was likely affected by a lateral influx of precipitation. Within 36 days of laboratory incubation, isotopically heavy DOC that had been initially released from the peat was replaced by isotopically lighter DOC, whose δ¹³C values converged to the solid substrate and natural run‐off. We suggest that δ¹³C systematics can be useful in identification of vertically stratified within‐bog DOC sources for peatland run‐off.     

Fluvial transport of suspended sediment and organic carbon during flood events in a large agricultural catchment in southwest France

Water draining from a large agricultural catchment of 1 110 km² in southwest France was sampled over an 18‐month period to determine the temporal variability in suspended sediment (SS) and dissolved (DOC) and particulate organic carbon (POC) transport during flood events, with quantification of fluxes and controlling factors, and to analyze the relationships between discharge and SS, DOC and POC. A total of 15 flood events were analyzed, providing extensive data on SS, POC and DOC during floods. There was high variability in SS, POC and DOC transport during different seasonal floods, with SS varying by event from 513 to 41 750 t; POC from 12 to 748 t and DOC from 9 to 218 t. Overall, 76 and 62% of total fluxes of POC and DOC occurred within 22% of the study period. POC and DOC export from the Save catchment amounted to 3090 t and 1240 t, equivalent to 1·8 t km^?2 y^?1 and 0·7 t km^?2 y^?1, respectively. Statistical analyses showed that total precipitation, flood discharge and total water yield were the major factors controlling SS, POC and DOC transport from the catchment. The relationships between SS, POC and DOC and discharge over temporal flood events resulted in different hysteresis patterns, which were used to deduce dissolved and particulate origins. In both clockwise and anticlockwise hysteresis, POC mainly followed the same patterns as discharge and SS. The DOC‐discharge relationship was mainly characterized by alternating clockwise and anticlockwise hysteresis due to dilution effects of water originating from different sources in the whole catchment. Copyright © 2011 John Wiley & Sons, Ltd.     

Export and degassing of terrestrial carbon through watercourses draining a temperate podzolized catchment

We measured spatial and temporal variations in carbon concentrations, isotopic compositions and exports during a complete hydrological cycle in nine watercourses draining a lowland forested podzolized catchment, flowing into the Arcachon lagoon (France). In addition, integrated fluxes of CO₂ across the water-atmosphere interface were estimated to assess the relative importance of CO₂ evasion versus lateral carbon transport at the catchment scale. Watercourse similarities and specificities linked to the local catchment characteristics are discussed and compared with other riverine systems. Low concentrations of suspended particulate matter and particulate organic carbon (POC) were generally measured in all the watercourses (8.4 ± 3.4 and 1.6 ± 0.6 mg L^?1, respectively), reflecting limited mechanical soil erosion. The generally high POC content in the suspended matter (20 %), low Chl a concentrations (1.3 ± 1.4 μg L^?1) and the relatively constant δ¹³C-POC value (near ?28 ‰) throughout the year reveal this POC originates from terrestrial C₃ plant and soil detritus. The presence of podzols leads to high levels of dissolved organic carbon (DOC; 6.6 ± 2.2 mg L^?1). Similarly, high dissolved inorganic carbon (DIC) concentrations were measured in the Arcachon lagoon catchment (5.9 ± 2.2 mg L^?1). The δ¹³C-DIC value around ?20 ‰ throughout the year in many small watercourses reveals the predominance of terrestrial carbon mineralisation and silicate rock weathering in soils as the major DIC source. With pCO₂ between 1,000 and 10,000 ppmv, all watercourses were a source of CO₂ to the atmosphere, particularly during the low river stage. Organic carbon parameters remained relatively stable throughout the year, whereas DIC parameters showed strong seasonal contrasts closely linked to the hydrological regime and hyporheic flows. In total, the carbon export from the Arcachon watershed was estimated at 15,870 t C year^?1 or 6 t C km^?2 year^?1, mostly exported to the lagoon as DOC (35 %), DIC (24 %) and lost as CO₂ degassing to the atmosphere (34 %).     

Dissolved organic carbon export from a cutover and restored peatland

High demand for horticultural peat has increased peatland drainage and peat extraction in Canada. The hydrology and carbon cycling of these cutover peatlands is greatly altered, necessitating active restoration efforts to permit the regeneration of Sphagnum mosses and the re‐establishment of natural peatland function. The effect of peatland extraction and restoration on the export of dissolved organic carbon (DOC) was examined for three successive seasons (May to October, 1999 to 2001) at two different sites (cutover and restored) in eastern Québec. A shift towards higher DOC concentrations was observed following peatland extraction (maximum: 182·6 mg L^?1) and concentrations remained high post‐restoration (maximum: 191·0 mg L^?1). The cutover site exported more DOC than the restored site in all three study seasons. The highest exports occurred during the wettest year (1999), with cutover and restored site export of 10·3 and 4·8 g m^?2, respectively. In 2000, 8·5 g C m^?2 was released from the cutover site, while the restored site released less than half that amount (3·4 g C m^?2). In 2001, the restored site released about the same amount of DOC as in the previous year (3·5 g C m^?2), while the cutover site load dropped to 6·2 g C m^?2. Both sites were net exporters of DOC in all years. Copyright © 2007 John Wiley & Sons, Ltd.     

Dissolved organic matter dynamics during the spring snowmelt at a boreal river valley mire complex in Northwest Russia

Boreal mire landscapes are rich in soil carbon and significantly contribute to the carbon input of aquatic ecosystems. They are composed of different mesoscale ecohydrological subunits, whose individual contributions to the water and carbon export of mire catchments are not well understood. The spring snowmelt period is the major hydrological event in the annual water cycle of the boreal regions and strongly influences the carbon flux between the terrestrial and aquatic systems. The aim of this study was (1) to provide a conceptual understanding of the spatial and temporal dynamics of the surface water chemistry along a swamp forest‐fen‐bog gradient during the snowmelt period, (2) to quantify the exported dissolved organic carbon (DOC) content in the runoff and (3) to identify the ecohydrological landscape unit that contributes most to DOC export during the snowmelt period in a heterogeneous mire complex in Northwest Russia. The highest DOC concentrations were detected in the swamp forest, and the lowest concentrations were observed at the treeless bog by the end of the snowmelt period (swamp forest: 37–43 mg l^?1, bog: 13–17 mg l^?1). During the spring snowmelt period, a significant amount (~1.7 g C m^?2) of DOC was transferred by the ~74 mm of runoff from the catchment into the river. Variability in the thawing periods led to differences in the relative contributions of each ecohydrological zone to the carbon export measured at a stream channel draining the studied part of the mire complex. An increased understanding of the variation in DOC concentrations and contributions from the mesoscale ecohydrological subunits to carbon export can help to predict the potential regional loss of DOC based on land cover type under climate change. Copyright © 2015 John Wiley & Sons, Ltd.     

Total waterborne carbon export and DOC composition from ten nested subarctic peatland catchments—importance of peatland cover,groundwater influence,and inter‐annual variability of precipitation patterns

Waterborne carbon (C) export from terrestrial ecosystems is a potentially important flux for the net catchment C balance and links the biogeochemical C cycling of terrestrial ecosystems to their downstream aquatic ecosystems. We have monitored hydrology and stream chemistry over 3 years in ten nested catchments (0.6–15.1 km²) with variable peatland cover (0%–22%) and groundwater influence in subarctic Sweden. Total waterborne C export, including dissolved and particulate organic carbon (DOC and POC) and dissolved inorganic carbon (DIC), ranged between 2.8 and 7.3 g m^–2 year^–1, representing ~10%–30% of catchment net ecosystem exchange of CO₂. Several characteristics of catchment waterborne C export were affected by interacting effects of peatland cover and groundwater influence, including magnitude and timing, partitioning into DOC, POC, and DIC and chemical composition of the exported DOC. Waterborne C export was greater during the wetter years, equivalent to an average change in export of ~2 g m^–2 year^–1 per 100 mm of precipitation. Wetter years led to a greater relative increase in DIC export than DOC export due to an inferred relative shift in dominance from shallow organic flow pathways to groundwater sources. Indices of DOC composition (SUVA₂₅₄ and a₂₅₀/a₃₆₅) indicated that DOC aromaticity and average molecular weight increased with catchment peatland cover and decreased with increased groundwater influence. Our results provide examples on how waterborne C export and DOC composition might be affected by climate change. Copyright © 2012 John Wiley & Sons, Ltd.     

The solute budget of a forest catchment and solute fluxes within a Pinus radiata and a secondary native forest site,southern Chile

Solute concentrations and fluxes in rainfall, throughfall and stemflow in two forest types, and stream flow in a 90 ha catchment in southern Chile (39°44′S, 73°10′W) were measured. Bulk precipitation pH was 6·1 and conductivity was low. Cation concentrations in rainfall were low (0·58 mg Ca²⁺ l^?1, 0·13 mg K⁺ l^?1, 0·11 mg Mg²⁺ l^?1 and <0·08 mg NH₄–N l^?1), except for sodium (1·10 mg l^?1). Unexpected high levels of nitrate deposition in rainfall (mean concentration 0·38 mg NO₃–N l^?1, total flux 6·3 kg NO₃–N ha^?1) were measured. Concentrations of soluble phosphorous in bulk precipitation and stream flow were below detection limits (<0·09 mg l^?1) for all events. Stream‐flow pH was 6·3 and conductivity was 28·3 μs. Stream‐water chemistry was also dominated by sodium (2·70 mg l^?1) followed by Ca, Mg and K (1·31, 0·70 and 0·36 mg l^?1). The solute budget indicated a net loss of 3·8 kg Na⁺ ha^?1 year^?1, 5·4 kg Mg²⁺ ha^?1 year^?1, 1·5 kg Ca²⁺ ha^?1 year^?1 and 0·9 kg K⁺ ha^?1 year^?1, while 4·9 kg NO₃–N ha^?1 year^?1 was retained by the ecosystem. Stream water is not suitable for domestic use owing to high manganese and, especially, iron concentrations. Throughfall and stemflow chemistry at a pine stand (Pinus radiata D. Don) and a native forest site (Siempreverde type), both located within the catchment, were compared. Nitrate fluxes within both forest sites were similar (1·3 kg NO₃–N ha^?1 year^?1 as throughfall). Cation fluxes in net rainfall (throughfall plus stemflow) at the pine stand generally were higher (34·8 kg Na⁺ ha^?1 year^?1, 21·5 kg K⁺ ha^?1 year^?1, 5·1 kg Mg²⁺ ha^?1 year^?1) compared with the secondary native forest site (24·7 kg Na⁺ ha^?1 year^?1, 18·9 kg K⁺ ha^?1 year^?1 and 4·4 kg Mg²⁺ ha^?1 year^?1). However, calcium deposition beneath the native forest stand was higher (15·9 kg Ca²⁺ ha^?1 year^?1) compared with the pine stand (12·6 kg Ca²⁺ ha^?1 year^?1). Copyright © 2002 John Wiley & Sons, Ltd.     

Soil carbon losses by sheet erosion: a potentially critical contribution to the global carbon cycle

Despite soil erosion through water being a ubiquitous process and its environmental consequences being well understood, its effects upon the global carbon cycle still remain largely uncertain. How much soil organic carbon (SOC) is removed each year from soils by sheet wash, an important if not the most efficient mechanism of detachment and transport of surficial soil material? What are the main environnemental controls worldwide? These are important questions which largely remain unanswered. Empirical data from 240 runoff plots studied over entire rainy seasons from different regions of the world were analysed to estimate particulate organic carbon (POC) losses (POC_L), and POC enrichment in the sediments compared to the bulk soil (ER), which can be used as a proxy of the fate of the eroded POC. The median POC_L was 9.9 g C m^‐2 y^‐1 with highest values observed for semi‐arid soils (POC_L = 10.8 g C m^‐2 y^‐1), followed by tropical soils (POC_L = 6.4 g C m^‐2 y^‐1) and temperate soils (POC_L = 1.7 g C m^‐2 y^‐1). Considering the mean POC_L of 27.2 g C m^‐2 y^‐1, the total amount of SOC displaced annually by sheet erosion from its source would be 1.32 ± 0.20 Gt C, i.e. 14.6% of the net annual fossil fuel induced C emissions of 9 Gt C. Because of low sediment enrichment in POC, erosion‐induced CO₂ emissions are likely to be limited in clayey environments while POC burial within hillslopes is likely to constitute an important carbon sink. In contrast, most of the POC displaced from sandy soils is likely to be emitted to the atmosphere. These results underpin the major role sheet wash plays in the displacement of SOC from its source and in the fate of the eroded SOC, with large variations across the different pedo‐climatic regions of the world. Copyright © 2015 John Wiley & Sons, Ltd.     

Net autotrophy in a fluvial lake: the relative role of phytoplankton and floating-leaved macrophytes

This study combined water- and sediment flux measurements with mass balances of dissolved gas and inorganic matter to determine the importance of pelagic and benthic processes for whole-system metabolism in a eutrophic fluvial lake. Mass balances of dissolved O₂, inorganic carbon (DIC), nitrogen (DIN), phosphorous (SRP), particulate N (PN) and P (PP) and Chl a were calculated at a nearly monthly frequency by means of repeated sampling at the lake inlet and outlet. Simultaneously, benthic fluxes of gas and nutrients, including denitrification rates, and the biomass of the dominant pleustophyte (Trapa natans) were measured, and fluxes of O₂ and CO₂ across the water–atmosphere interface were estimated from diel changes in outlet concentrations. On an annual scale, Middle Lake exhibited CO₂ supersaturation, averaging 313% (range 86–562%), but was autotrophic with a net O₂ production (6.35 ± 2.05 mol m⁻² y⁻¹), DIC consumption (−31.18 ± 18.77 mol m⁻² y⁻¹) and net export of Chl a downstream (8.38 ± 0.95 mol C m⁻² y⁻¹). Phytoplankton was the main driver of Middle Lake metabolism, with a net primary production estimated at 33.24 mol O₂ m⁻² y⁻¹, corresponding to a sequestration of 4.18 and 0.26 mol m⁻² y⁻¹ of N and P, respectively. At peak biomass, T. natans covered about 18% of Middle Lake’s surface and fixed 2.46, 0.17 and 0.02 mol m⁻² of C, N and P, respectively. Surficial sediments were a sink for O₂ (−14.47 ± 0.65 mol O₂ m⁻² y⁻¹) and a source of DIC and NH₄ ⁺ (18.84 ± 2.80 mol DIC m⁻² y⁻¹ and 0.83 ± 0.16 mol NH₄ ⁺ m⁻² y⁻¹), and dissipated nitrate via denitrification (1.44 ± 0.11 mol NO₃ ⁻ m⁻² y⁻¹). Overall, nutrient uptake by primary producers and regeneration from sediments were a minor fraction of external loads. This work suggests that the creation of fluvial lakes can produce net autotrophic systems, with elevated rates of phytoplanktonic primary production, largely sustained by allochtonous nutrient inputs. These hypereutrophic aquatic bodies are net C sinks, although they simultaneously release CO₂ to the atmosphere.     

Studies on Primary Productivity and some Hydrochemical Aspects of a Polluted Water-body of the Himalayan Jhelum Valley

The lake without any outlet (11 ha, 55000 m³, z_max 2,25 m) has a weak thermal stratification with maximum surface temperatures of 32.5 °C. The annual variation of temperature and depth of visibility is unimodal, with the maxima or minima in August. Phytoplankton consists mainly of Cyanophyceae. The primary production determined by the light-dark bottle technique (oxygen method) varies in the annual variation between 0.3… 0.5 g m^?2 d^?1 C (winter) and 3.4… 4.6 g m^?2 d^?1 C (summer); as the annual means of 1975 and 1976 there were found 1.9 and 2.4 g m^?2 d^?1 C, resp., gross production at a utilization of 0.42… 2.85% of the radiation energy. The chemism is a well-buffered hydrogen-carbonate water (pH 8.1… 9.0) with 74… 90 mg/1 Na and 20.5… 31.5 mg/1 K and with a good nutrient supply (20… 40 μg/1 PO₄—P and 100… 240 μg/1 NO₃—N) at the same time.     

Estimating suspended sediment concentrations from turbidity measurements and the calibration problem

In situ turbidity meters are being increasingly used to generate continuous records of suspended sediment concentration in rivers. However, the usefulness of the information obtained depends heavily on the existence of a close relationship between fluctuations in suspended sediment concentration and turbidity and the calibration procedure that relates suspended sediment concentration to the turbidity meter's signal. This study assesses the relationship between suspended sediment concentration and turbidity for a small (1·19 km²) rural catchment in southern Brazil and evaluates two calibration methods by comparing the estimates of suspended sediment concentration obtained from the calibrated turbidity readings with direct measurements obtained using a USDH 48 suspended sediment sampler. With the first calibration method, the calibration relationship is derived by relating the turbidity readings to simultaneous measurements of concentration obtained from suspended sediment samples collected from the vicinity of the turbidity probe during flood events. With the second method, the calibration is based on the readings obtained from the turbidity meter when the probe immersed in samples of known concentration prepared using soils collected from the catchment. Overall, there was a close link between fluctuations in suspended sediment concentration and turbidity in the stream at the outlet of the catchment, and the estimates of sediment concentration obtained using the first calibration method corresponded closely with the conventionally measured sediment concentrations. However, use of the second calibration method introduced appreciable errors. When the estimated sediment concentrations were compared with the measured values, the mean errors were ± 122 mg l^?1 and + 601 mg l^?1 for the first and second calibration procedures respectively. Copyright © 2007 John Wiley & Sons, Ltd.     

Hydrological heterogeneity of an alpine stream–lake network in Switzerland

Water source and lake landscape position can strongly influence the physico‐chemical characteristics of flowing waters over space and time. We examined the physico‐chemical heterogeneity in surface waters of an alpine stream‐lake network (>2600 m a.s.l.) in Switzerland. The catchment comprises two basins interspersed with 26 cirque lakes. The larger lakes in each basin are interconnected by streams that converge in a lowermost lake with an outlet stream. The north basin is primarily fed by precipitation and groundwater, whereas the south basin is fed mostly by glacial melt from rock glaciers. Surface flow of the entire channel network contracted by ～60% in early autumn, when snowmelt runoff ceased and cold temperatures reduced glacial outputs, particularly in the south basin. Average water temperatures were ～4 °C cooler in the south basin, and temperatures increased by about 4–6 °C along the longitudinal gradient within each basin. Although overall water conductivity was low (<27 µS cm^?1) because of bedrock geology (ortho‐gneiss), the south basin had two times higher conductivity values than the north basin. Phosphate‐phosphorus levels were below analytical detection limits, but particulate phosphorus was about four times higher in the north basin (seasonal average: 9 µg l^?1) than in the south basin (seasonal average: 2 µg l^?1). Dissolved nitrogen constituents were around two times higher in the south basin than in the north basin, with highest values averaging > 300 µg l^?1 (nitrite + nitrate‐nitrogen), whereas particulate nitrogen was approximately nine times greater in the north basin (seasonal average: 97 µg l^?1) than in the south basin (seasonal average: 12 µg l^?1). Total inorganic carbon was low (usually <0·8 mg l^?1), silica was sufficient for algal growth, and particulate organic carbon was 4·5 times higher in the north basin (average: 0·9 mg l^?1) than in the south basin (average: 0·2 mg l^?1). North‐basin streams showed strong seasonality in turbidity, particulate‐nitrogen and ‐phosphorus, and particulate organic carbon, whereas strong seasonality in south‐basin streams was observed in conductivity and dissolved nitrogen. Lake position influenced the seasonal dynamics in stream temperatures and nutrients, particularly in the groundwater/precipitation‐fed north‐basin network. Copyright © 2007 John Wiley & Sons, Ltd.     

Greenhouse gas emissions (CO2, CH4, and N2O) from several perialpine and alpine hydropower reservoirs by diffusion and loss in turbines

We investigated greenhouse gas emissions (CO₂, CH₄, and N₂O) from reservoirs located across an altitude gradient in Switzerland. These are the first results of greenhouse gas emissions from reservoirs at high elevations in the Alps. Depth profiles were taken in 11 reservoirs located at different altitudes between the years 2003 and 2006. Diffusive trace gas emissions were calculated using surface gas concentrations, wind speeds and transfer velocities. Additionally, methane entering with the inflowing water and methane loss at the turbine was assessed for a subset of the reservoirs. All reservoirs were emitters of carbon dioxide and methane with an average of 970?±?340?mg?m^?2?day^?1 (results only from four lowland and one subalpine reservoir) and 0.20?±?0.15?mg?m^?2?day^?1, respectively. One reservoir (Lake Wohlen) emitted methane at a much higher rate (1.8?±?0.9?mg?m^?2?day^?1) than the other investigated reservoirs. There was no significant difference in methane emissions across the altitude gradient, but average dissolved methane concentrations decreased with increasing elevation. Only lowland reservoirs were sources for N₂O (72?±?22???g?m^?2?day^?1), while the subalpine and alpine reservoirs were in equilibrium with atmospheric concentrations. These results indicate reservoirs from subalpine/alpine regions to be only minor contributors of greenhouse gases to the atmosphere compared to other reservoirs.     

Riverine export of water,sediment and carbon during flood events in the arid to semi-arid Wuding River on the Chinese Loess Plateau

Floods have become increasingly important in fluvial export of water, sediment and carbon (C). Using high-frequency sampling, the export of water, sediment and C was examined in the Wuding River catchment on the Chinese Loess Plateau. With groundwater as an important contributor to runoff all year round, floods were relatively less important in the export of water. However, large floods were disproportionately important in exporting sediment and inorganic C (DIC) and organic C (DOC and POC). The three largest floods in each year transported 53.6–97.3 and 41.4–77% of the annual sediment and C fluxes, respectively. An extreme flood in 2017 alone contributed 94.6 and 73.1% of the annual sediment and C fluxes, respectively, in just 7 days, which included 20.3, 92.1 and 35.7% of the annual DOC, POC and DIC fluxes, respectively. A stable carbon isotope (δ¹³C) analysis of POC indicated that modern soils and C3 plants were its primary source. Furthermore, floods greatly accelerated CO₂ degassing due to elevated gas transfer velocity, although stream water CO₂ partial pressure (pCO₂) exhibited a decreasing trend with flow discharge. Although these results illustrated that increasing runoff diluted pCO₂, the timing and magnitude of floods were found to be critical in determining the response of pCO₂ to flow dynamics. Low-magnitude floods in the early wet season increased pCO₂ because of enhanced organic matter input, while subsequent large floods caused a lower pCO₂ due to greatly reduced organic matter supply. Finally, continuous monitoring of a complete flood event showed that the CO₂ efflux during the flood (2348 ± 664 mg C m^–2 day^–1) was three times that under low-flow conditions (808 ± 98 mg C m^–2 day^–1). Our study suggests that infrequent, heavy storm events, which are predicted to increase under climate change, will greatly alter the transport regimes of sediment and C. © 2020 John Wiley & Sons, Ltd.     

Landscape influences on aluminium and dissolved organic carbon in streams draining the Hubbard Brook valley,New Hampshire,USA

Concentrations of both aluminium (Al) and dissolved organic carbon (DOC) in stream waters are likely to be regulated by factors that influence water flowpaths and residence times, and by the nature of the soil horizons through which waters flow. In order to investigate landscape‐scale spatial patterns in streamwater Al and DOC, we sampled seven streams draining the Hubbard Brook valley in central New Hampshire. We observed considerable variation in stream chemistry both within and between headwater watersheds. Across the valley, concentrations of total monomeric aluminium (Al_m) ranged from below detection limits (<0·7 µmol l⁻¹) to 22·3 µmol l⁻¹. In general, concentrations of Al_m decreased as pH increased downslope. There was a strong relationship between organic monomeric aluminium (Al_o) and DOC concentrations (R² = 0·92). We observed the highest Al_m concentrations in: (i) a watershed characterized by a steep narrow drainage basin and shallow soils and (ii) a watershed characterized by exceptionally deep forest floor soils and high concentrations of DOC. Forest floor depth and drainage area together explained much of the variation in ln Al_m (R² = 0·79; N = 45) and ln DOC (R² = 0·87; N = 45). Linear regression models were moderately successful in predicting ln Al_m and ln DOC in streams that were not included in model building. However, when back‐transformed, predicted DOC concentrations were as much as 72% adrift from observed DOC concentrations and Al_m concentrations were up to 51% off. This geographic approach to modelling Al and DOC is useful for general prediction, but for more detailed predictions, process‐level biogeochemical models are required. Copyright © 2005 John Wiley & Sons, Ltd.     

Selective organic carbon losses from soils by sheet erosion and main controls

Although the impact of sheet erosion on the selective transportation of mineral soil particles has been widely investigated, little is yet known about the specific mechanisms of organic carbon (OC) erosion, which constitutes an important link in the global carbon cycle. The present study was conducted to quantify the impact of sheet erosion on OC losses from soils. Erosion plots with the lengths of 1‐ and 5‐m were installed at different topographic positions along a hillslope in a mountainous South African region. A total of 32 rainfall events from a three years period (November 2010 up to February 2013), were studied and evaluated for runoff (R), particulate and dissolved organic carbon (POC_L and DOC_L). In comparison to the 0–0·05 m bulk soil, the sediments from the 1‐m plots were enriched in OC by a factor 2·6 and those from the 5‐m long plots by a factor of 2·2, respectively. These findings suggest a preferential erosion of OC. In addition, total organic carbon losses (TOC_L) were incurred mainly in particulate form (~94%) and the increase in TOC_L from 14·09 ± 0·68 g C m^?1 yr^?1 on 1‐m plots to 50·03 ± 2·89 g C m^?1 yr^?1 on 5‐m plots illustrated an increase in sheet erosion efficiency with increasing slope length. Both TOC_L and sediment enrichment in OC correspondingly increased with a decrease in soil basal grass cover. The characteristics of rainstorms had no significant impact on the selectivity of OC erosion. The results accrued in this study investigating the links between sheet erosion and OC losses, are expected to be of future value in the generation of carbon specific erosion models, which can further help to inform and improve climate change mitigation measures. Copyright © 2016 John Wiley & Sons, Ltd.     

Zur Rolle der Stickstoffixation im Stoffhaushalt eines geschichteten Sees

In the dimict lake Arend (5.1 km², 146 hm³, 49.5 m z_max), nitrogen is production-limiting with concentrations below the detection limit during the production period. Phytoplankton achieves biomasses of up to 18 mg/l fresh matter, essential contributions being made by Aphanizomenon with 2 mg/l and Anabaena with up to 10 mg/l. Nitrogen fixation was measured by the ethine reduction technique (acetylene reduction) during periods of the occurrence of heterocystforming Cyanophyceae and achieved peak values up to 6.59 μg N² · h^?1 · l^?1 or 14.87 m^?2 · h^?1 g N₂ · m^?2 · h^?1. The rates of fixation show a safe correlation with the biomass of heterocyst-containing Cyanophyceae (r = 0.88), their development beginning at values below the N : P-ratio of 2.66.