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1.
Fred Worrall  Tim Burt 《水文研究》2005,19(9):1791-1806
The dissolved CO2 concentration of stream waters is an important component of the terrestrial carbon cycle. This study reconstructs long‐term records of dissolved CO2 concentration for the outlets of two large catchments (818 and 586 km2) in northern England. The study shows that:
  • 1. The flux of dissolved CO2 from the catchments (as carbon per catchment area), when adjusted for that which would be carried by the river water at equilibrium with the atmosphere, is between 0 and 0·39 t km−2 year−1 for the River Tees and between 0 and 0·65 t km−2 year−1 for the River Coquet.
  • 2. The flux of dissolved CO2 is closely correlated with dissolved organic carbon (DOC) export and is unrelated to dissolved CO2 export from the headwaters of the study catchments.
  • 3. The evasion rate of CO2 from the rivers (as carbon per stream area) is between 0·0 and 1·49 kg m−2 year−1, and calculated in‐stream productions of CO2 are estimated as between 0·5 and 2·5% of the stream evasion rate.
  • 4. By mass balance, it is estimated that 8% of the annual flux of DOC is lost within the streams of the catchment.
The study shows that the loss of CO2 from the streams of the Tees catchment is between 3·1 and 7·5 kt year−1 (as carbon) for the River Tees, which is the same order as annual CH4 flux from peats within the catchment and approximately 50% of the net CO2 exchange to the peats of the catchment. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

2.
This study involved a baseline evaluation of fluvial carbon export and degas rates in three nested rural catchments (1 to 80 km2) in Taboão, a representative experimental catchment of the Upper Uruguay River Basin. Analyses of the carbon content in stream waters and the catchment carbon yield were based on 4‐year monthly in situ data and statistical modeling using the United States Geological Survey load estimator model. We also estimated p CO2 and degas fluxes using carbonate equilibrium and gas‐exchange formulas. Our results indicated that the water was consistently p CO2 saturated (~90% of the cases) and that the steep terrain favors high gas evasion rates. The mean calculated fluvial export was 5.4 tC·km?2·year?1 with inorganic carbon dominating (dissolved inorganic carbon:dissolved organic carbon ratio >4), and degas rates (~40 tC km?2·year?1) were nearly sevenfold higher than the downstream export. The homogeneous land use in this nested catchment system results in similar water‐quality characteristics, and therefore, export rates are expected to be closely related to the rainfall–runoff relationships at each scale. Although the sampling campaigns did not fully reproduce storm‐event conditions and related effects such as flushing or dilution of in‐stream carbon, our results indicated a potential link between dissolved inorganic carbon and slower hydrological pathways related to subsurface water storage and movement.  相似文献   

3.
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.  相似文献   

4.
Utilising newly available instrumentation, the carbon balance in two small tropical catchments was measured during two discharge events at high temporal resolution. Catchments share similar climatic conditions, but differ in land use with one draining a pristine rainforest catchment, the other a fully cleared and cultivated catchment. The necessity of high resolution sampling in small catchments was illustrated in each catchment, where significant chemical changes occurred in the space of a few hours or less. Dissolved and particulate carbon transport dominated carbon export from the rainforest catchment during high flow, but was surpassed by degassing of CO2 less than 4 h after the discharge peak. In contrast, particulate organic carbon dominated export from the cleared catchment, in all flow conditions with CO2 evasion accounting for 5–23% of total carbon flux. Stable isotopes of dissolved inorganic carbon (DIC) in the ephemeral rainforest catchment decreased quickly from ~1.5 ‰ to ~ ?16 ‰ in 5 h from the flood beginning. A two‐point mixing model revealed that in the initial pulse, over 90% of the DIC was of rainwater origin, decreasing to below 30% in low flow. In the cultivated catchment, δ13CDIC values varied significantly less (?11.0 to ?12.2 ‰) but revealed a complex interaction between surface runoff and groundwater sources, with groundwater DIC becoming proportionally more important in high flow, due to activation of macropores downstream. This work adds to an increasing body of work that recognises the importance of rapid, short‐lived hydrological events in low‐order catchments to global carbon dynamics. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

5.
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 %).  相似文献   

6.
Estimates of greenhouse gas evasion from rivers have been refined over the past decades to constrain their role in global carbon cycle processes. However, despite 55% of the human population living in urban areas, urban rivers have had limited attention. We monitored carbon dynamics in an urbanized river (River Kelvin, 331 km2, UK) to explore the drivers of dissolved carbon lateral and vertical export. Over a 2-year sampling period, riverine methane (CH4) and carbon dioxide (CO2) concentrations were consistently oversaturated with respect to atmospheric equilibria, leading to continual degassing to the atmosphere. Carbon stable isotopic compositions (δ13C) indicated that terrestrially derived carbon comprised most of the riverine CH4 and dissolved CO2 (CO2*) load while dissolved inorganic carbon (DIC) from groundwater was the main form of riverine DIC. The dynamics of CH4, CO2*, and DIC in the river were primarily hydrology-controlled, that is, [CH4] and [CO2*] both increased with elevated discharge, total [DIC] decreased with elevated discharge while the proportion of biologically derived DIC increased with increasing discharge. The concentration of dissolved organic carbon (DOC) showed a weak relationship with river hydrology in summer and autumn and was likely influenced by the combined sewer overflows. Carbon emission to the atmosphere is estimated to be 3.10 ± 0.61 kg C·m−2·yr−1 normalized to water surface area, with more than 99% emitted as CO2. Annual carbon loss to the coastal estuary is approximately 4.69 ± 0.70 Gg C yr−1, with annual DIC export approximately double that of DOC. Per unit area, the River Kelvin was a smaller carbon source to the atmosphere than natural rivers/streams but shows elevated fluxes of DIC and DOC under comparable conditions. This research illustrates the role urban systems may have on riverine carbon dynamics and demonstrates the potential tight link between urbanization and riverine carbon export.  相似文献   

7.
To investigate the effects of anthropogenic activity, namely, land use change and reservoir construction, on particulate organic carbon (POC) transport, we collected monthly water samples during September 2007 to August 2009 from the Longchuanjiang River to understand seasonal variations in the concentrations of organic carbon species and their sources and the yield of organic and inorganic carbon from the catchment in the Upper Yangtze basin. The contents of riverine POC, total organic carbon and total suspended sediment (TSS) changed synchronously with water discharge, whereas the contents of dissolved organic carbon had a small variation. The POC concentration in the suspended sediment decreased non‐linearly with increasing TSS concentration. Higher molar C/N ratio of particulate organic matter (average 77) revealed that POC was dominated by terrestrially derived organic matter in the high flows and urban wastewaters in the low flows. The TSS transported by this river was 2.7 × 105 t/yr in 2008. The specific fluxes of total organic carbon and dissolved inorganic carbon (DIC) were 5.6 and 6 t/km2/yr, respectively, with more than 90% in the high flow period. A high carbon yield in the catchment of the upper Yangtze was due to human‐induced land use alterations and urban wastes. Consistent with most rivers in the monsoon climate regions, the dissolved organic carbon–POC ratio of the export flux was low (0.41). Twenty‐two percent (0.9 t/km2/yr) of POC out of 4 t/km2/yr was from autochthonous production and 78% (3.1 t/km2/yr) from allochthonous production. The annual sediment load and hence the organic carbon flux have been affected by environmental alterations of physical, chemical and hydrological conditions in the past 50 years, demonstrating the impacts of human disturbances on the global and local carbon cycling. Finally, we addressed that organic carbon flux should be reassessed using adequate samples (i.e. at least two times in low‐flow month, four times in high‐flow month and one time per day during the flood period), daily water discharge and sediment loads and appropriate estimate method. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

8.
Dissolved inorganic carbon (DIC) is the most important carbon component in karst aquatic system where fluid is highly transmissive, but has rarely been examined in the subtropical karst critical zone (K-CZ). In this study, concentrations of dissolved solutes and isotopic compositions of DIC (δ13CDIC) at 11 sites of a 73.4 km2 karstic catchment in Southwestern China were analysed monthly in order to uncover the spatiotemporal variations of both DIC and its dominant sources, and to identify relevant controlling factors. Both DIC concentrations and δ13CDIC were highly variable, ranging from 2.52 to 5.85 mmol l−1 and from −15.7 to −4.5‰, respectively. DIC in underground water (UGW) was higher in concentration and more depleted in 13C compared to surface water (SFS). DIC concentrations showed an inconsistent seasonal trend with other solutes, with higher values in the wet season at some sites. δ13CDIC values were lower in the wet season than in the dry season. The results of mixing model IsoSource revealed spatiotemporal patterns of DIC sources. During the dry season, carbonate weathering was the primary contributor to DIC in UGW (excluding in the middle reaches). However, during the wet season, soil CO2 was the dominant source of DIC in both UGW and SFS, and it was higher than in the dry season. Overall, there are significant spatiotemporal disparities and highly transmissive characteristics of both DIC and its sources in the K-CZ, which are controlled by multiple factors. This study also highlights that rainfall may play a crucial role in accelerating carbon dynamics in the K-CZ. High-frequency sampling campaigns in high-flow periods and deep analyses are needed in future work to elucidate the related processes and mechanisms. © 2019 John Wiley & Sons, Ltd.  相似文献   

9.
The stable isotopic composition of dissolved inorganic carbon (δ13C‐DIC) was investigated as a potential tracer of streamflow generation processes at the Sleepers River Research Watershed, Vermont, USA. Downstream sampling showed δ13C‐DIC increased between 3–5‰ from the stream source to the outlet weir approximately 0·5 km downstream, concomitant with increasing pH and decreasing PCO2. An increase in δ13C‐DIC of 2·4 ± 0·1‰ per log unit decrease of excess PCO2 (stream PCO2 normalized to atmospheric PCO2) was observed from downstream transect data collected during snowmelt. Isotopic fractionation of DIC due to CO2 outgassing rather than exchange with atmospheric CO2 may be the primary cause of increased δ13C‐DIC values downstream when PCO2 of surface freshwater exceeds twice the atmospheric CO2 concentration. Although CO2 outgassing caused a general increase in stream δ13C‐DIC values, points of localized groundwater seepage into the stream were identified by decreases in δ13C‐DIC and increases in DIC concentration of the stream water superimposed upon the general downstream trend. In addition, comparison between snowmelt, early spring and summer seasons showed that DIC is flushed from shallow groundwater flowpaths during snowmelt and is replaced by a greater proportion of DIC derived from soil CO2 during the early spring growing season. Thus, in spite of effects from CO2 outgassing, δ13C of DIC can be a useful indicator of groundwater additions to headwater streams and a tracer of carbon dynamics in catchments. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

10.
The extensive blanket peatlands of the UK uplands account for almost half of total national terrestrial carbon storage. However, much of the blanket peat is severely eroded so that the contemporary role of the peatland system in carbon sequestration is compromised by losses of organic carbon in dissolved (DOC) and particulate (POC) form in the fluvial system. This paper presents the first detailed assessment of dissolved and organic carbon losses from a severely eroded headwater peatland (River Ashop, South Pennines, UK). Total annual fluvial organic carbon losses range from 29–106 Mg C km,‐2 decreasing from the headwaters to the main catchment outlet. In contrast to less eroded systems fluvial organic carbon flux is dominated by POC. POC:DOC ratios decrease from values of 4 in the headwaters to close to unity at the catchment outlet. These results demonstrate the importance of eroding headwater sites as sources of POC to the fluvial system. Comparison with a range of catchment characteristics reveals that drainage density is the best predictor of POC:DOC but there is scatter in the relation in the headwaters. Steep declines in specific POC yield from headwater catchments are consistent with storage of POC within the fluvial system. Key to the significance of fluvial carbon flux in greenhouse gas budgets is understanding the fate of fluvial carbon. Further work on the fate of POC and the role of floodplains in fluvial carbon cycling is urgently required. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

11.
Globally, dissolved inorganic carbon (DIC) accounts for more than half the annual flux of carbon exported from terrestrial ecosystems via rivers. Here, we assess the relative influences of biogeochemical and hydrological processes on DIC fluxes exported from a tropical river catchment characterized by distinct land cover, climate and geology transition from the wet tropical mountains to the low‐lying savanna plains. Processes controlling changes in river DIC were investigated using dissolved organic carbon, particulate organic carbon and DIC concentrations and stable isotope ratios of DIC (δ13CDIC) at two time scales: seasonal and diel. The recently developed Isotopic Continuous Dissolved Inorganic Carbon Analyser was used to measure diel DIC concentration and δ13CDIC changes at a 15‐min temporal resolution. Results highlight the predominance of biologically mediated processes (photosynthesis and respiration) controlling diel changes in DIC. These resulted in DIC concentrations varying between 3.55 and 3.82 mg/l and δ13CDIC values ranging from ?19.7 ± 0.31‰ to ?17.1 ± 0.08‰. In contrast, at the seasonal scale, we observed wet season DIC variations predominantly from mixing processes and dry season DIC variations due to both mixing processes and biological processes. The observed wet season increases in DIC concentrations (by 6.81 mg/l) and δ13CDIC values of river water (by 5.4‰) largely result from proportional increases in subsurface inflows from the savanna plains (C4 vegetation) region relative to inflows from the rainforest (C3 vegetation) highlands. The high DIC river load during the wet season resulted in the transfer of 97% of the annual river carbon load. Therefore, in this gaining river, there are significant seasonal variations in both the hydrological and carbon cycles, and there is evidence of substantial coupling between the carbon cycles of the terrestrial and the fluvial environments. Recent identification of a substantial carbon sink in the savannas of northern Australia during wetter years in the recent past does not take into account the possibility of a substantial, rapid, lateral flux of carbon to rivers and back to the atmosphere. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

12.
Agricultural, forestry-impacted and natural catchments are all vectors of nutrient loading in the Nordic countries. Here, we present concentrations and fluxes of total nitrogen (totN) and phosphorus (totP) from 69 Nordic headwater catchments (Denmark: 12, Finland:18, Norway:17, Sweden:22) between 2000 and 2018. Catchments span the range of Nordic climatic and environmental conditions and include natural sites and sites impacted by agricultural and forest management. Concentrations and fluxes of totN and totP were highest in agricultural catchments, intermediate in forestry-impacted and lowest in natural catchments, and were positively related %agricultural land cover and summer temperature. Summer temperature may be a proxy for terrestrial productivity, while %agricultural land cover might be a proxy for catchment nutrient inputs. A regional trend analysis showed significant declines in N concentrations and export across agricultural (−15 μg totN L−1 year−1) and natural (−0.4 μg NO3-N L−1 year−1) catchments, but individual sites displayed few long-term trends in concentrations (totN: 22%, totP: 25%) or export (totN: 6%, totP: 9%). Forestry-impacted sites had a significant decline in totP (−0.1 μg P L−1 year−1). A small but significant increase in totP fluxes (+0.4 kg P km−2 year−1) from agricultural catchments was found, and countries showed contrasting patterns. Trends in annual concentrations and fluxes of totP and totN could not be explained in a straightforward way by changes in runoff or climate. Explanations for the totN decline include national mitigation measures in agriculture international policy to reduced air pollution and, possibly, large-scale increases in forest growth. Mitigation to reduce phosphorus appears to be more challenging than for nitrogen. If the green shift entails intensification of agricultural and forest production, new challenges for protection of water quality will emerge possible exacerbated by climate change. Further analysis of headwater totN and totP export should include seasonal trends, aquatic nutrient species and a focus on catchment nutrient inputs.  相似文献   

13.
From 2011 to 2019, mercury (Hg) stores and fluxes were studied in the small forested catchment Lesní potok (LES) in the central Czech Republic using the watershed mass balance approach together with internal measurements. Mean input fluxes of Hg via open bulk deposition, beech throughfall and spruce throughfall during the periodwere 2.9, 3.9 and 7.6 μg m−2 year−1, respectively. These values were considerably lower than corresponding deposition Hg fluxes reported in the early years of the 21st century from catchments in Germany. Current bulk precipitation inputs at unimpacted Czech mountainous sites were lower than those in Germany. The largest Hg inputs to the catchment were via litterfall, averaging 22.6 and 17.8 μg m−2 year−1 for beech and spruce stands. The average Hg input, based on the sum of mean litterfall and throughfall deposition, was 23.0 μg m−2 year−1, compared to the estimated Hg output in runoff of 0.5 μg m−2 year−1, which is low compared to other reported values. Thus, only ~2% of Hg input is exported in stream runoff. Stream water Hg was only weakly related to dissolved organic carbon (DOC) but both concentrations were positively correlated with water temperature. The estimated total soil Hg pool averaged 47.5 mg m−2, only 4% of which was in the O-horizon. Thus Hg in the O-horizon pool represents 72 years of deposition at the current input flux and 3800 years of export at the current runoff flux. Age-dating by 14C suggested that organic soil contains Hg from recent deposition, while mineral soil at 40–80 cm depth contained 4400-year old carbon, suggesting the soil had accumulated atmospheric Hg inputs through millennia to reach the highest soil Hg pool of the soil profile. These findings suggest that industrial era intensification of the Hg cycle is superimposed on a slower-paced Hg cycle during most of the Holocene.  相似文献   

14.
This paper considers the contributions of epigenic karst processes as a major element of the carbon cycle and a significant agent of landscape evolution. Geochemical models developed from monitoring data and water samples are used to estimate the variation and magnitude of dissolved inorganic carbon (DIC) flux in karst landscapes at several scales, from local to global. At the local scale, the Cumberland River watershed of southeast Kentucky, these geochemical models are also used to evaluate the potential role of sulfur in the production of DIC and to compute an estimated rate of landscape erosion. Geochemical modeling using ionic species and modeled discharge reveal a variable rate of DIC flux driven by large fluctuations in calcite saturation and discharge. Ratios of reaction products and principal component analyses (PCA) suggest that some bedrock dissolution may be driven by the oxidation of reduced sulfur derived from brines entrained into the karst aquifers. Over the 3730 km2 of carbonate exposure in the Cumberland River, 25.8–62.4 Gg/yr of carbon dioxide (CO2) is conveyed from the atmosphere through the dissolution of carbonate. At the global scale, this translates to 123–296 Tg/yr of CO2 delivered by karst processes into the aqueous system. The bedrock portion of DIC equates to a flux of 32.6 ± 2.6 m3 – 35.2 ± 2.8 m3 of bedrock during the period of study of which 29% was dolomite. This translates to a landscape erosion rate of 13.1–17.9 mm/ka in the 3.45–4.32 km2 of carbonate exposure in the studied watershed. Based upon 16+ km of cave survey data spanning a vertical range of 72 to 75 m above base level, this suggests that cave development in the watershed spans the Plio‐Pleistocene. Using the modeled erosion rates, the ages of cave levels, 4.03–5.71, 3.08–4.56, 1.57–2.43, 1.01–1.67, 0.45–0.91, and < 0.45 Ma, are in good agreement with regional studies of Plio‐Pleistocene landscape evolution in the Appalachian Lowland Plateaus. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

15.
The purposes of this study were to assess if Lake Apopka (FL, USA) was autotrophic or heterotrophic based on the partial pressure of dissolved carbon dioxide (pCO2) in the surface water and to evaluate factors that influence the long-term changes in pCO2. Monthly average pH, alkalinity and other limnological variables collected between 1987 and 2006 were used to estimate dissolved inorganic carbon (DIC), pCO2 and CO2 flux between surface water and atmosphere. Results indicated that average pCO2 in the surface water was 196 μatm, well below the atmospheric pCO2. Direct measurements of DIC concentration on three sampling dates in 2009 also supported pCO2 undersaturation in Lake Apopka. Supersaturation in CO2 occurred in this lake in only 13% of the samples from the 20-year record. The surface-water pCO2 was inversely related to Chl a concentrations. Average annual CO2 flux was 28.2 g C m−2 year−1 from the atmosphere to the lake water and correlated significantly with Chl a concentration, indicating that biological carbon sequestration led to the low dissolved CO2 concentration. Low pCO2 and high invasion rates of atmospheric CO2 in Lake Apopka indicated persistent autotrophy. High rates of nutrient loading and primary production, a high buffering capacity, a lack of allochthonous loading of organic matter, and the dominance of a planktivorous–benthivorous fish food web have supported long-term net autotrophy in this shallow subtropical eutrophic lake. Our results also showed that lake restoration by the means of nutrient reduction resulted in significantly lower total phosphorus (TP) and Chl a concentrations, and higher pCO2.  相似文献   

16.
Dissolved inorganic carbon (DIC) transport by rivers is an important control on the pH and carbonate chemistry of the coastal ocean. Here, we combine DIC and total alkalinity (TAlk) concentrations from four tropical rivers of the Great Barrier Reef region in Australia with daily river discharge to quantify annual river loads and export rates. DIC in the four rivers ranged from 284 to 2,639 μmol kg−1 and TAlk ranged from 220 to 2,612 μmol kg−1. DIC:TAlk ratios were mostly greater than one suggesting elevated exports of free [CO2*]. This was pronounced in the Johnstone and Herbert rivers of the tropical wet north. The largest annual loads were transported in the two large river catchments of the southern Great Barrier Reef region, the Fitzroy and Burdekin rivers. The carbon stable isotopic composition of DIC suggests that carbonate weathering was the dominant source of DIC in the southern rivers, and silicate weathering was likely a source of DIC in the northern Wet Tropics rivers. Annual loads and export rates were strongly driven by precipitation and discharge patterns, the occurrence of tropical cyclones, and associated flooding events, as well as distinct seasonal dry and wet periods. As such, short-lived hydrological events and long-term (seasonal and inter-annual) variation of DIC and TAlk that are pronounced in rivers of the tropical and subtropical wet and dry climate zone should be accounted for when assessing inorganic carbon loads to the coastal ocean and the potential to buffer against or accelerate ocean acidification.  相似文献   

17.
Fluvial organic carbon (OC) transformations are an important component of carbon cycling and greenhouse gas production in inland waters resulting in considerable recent interest in the fate of fluvial OC exported from carbon rich soils such as peatlands. Additionally, peatland catchments are important drinking water collection areas, where high OC concentrations in runoff have water treatment implications. This analysis presents the results from a year‐round intensive study within a water treatment catchment draining an area of peatland, considering carbon transformations along a continuum from headwater river, through a storage reservoir and pipe, to a water treatment works. The study uses a unique combination of methods (colourmetric, ultrafiltration, and 14C radiocarbon dating) to assess catchment wide changes in fluvial carbon composition (colour, size, and age) alongside concentration measures. The results indicate clear patterns of carbon transformations in the river and reservoir and dissolved low molecular weight coloured carbon to be most subject to change, with both loss and replacement within the catchment residence time. Although the evidence suggests dissolved OC (DOC) gains are from particulate OC breakdown, the mechanisms of DOC loss are less certain and may represent greenhouse gas losses or conversions to particulate OC. The transformations presented here appear to have minimal impact on the amount of harder to treat (<10 kDa) dissolved carbon, although they do have implications for total DOC loading to water treatment works. This paper shows that peatland fluvial systems are not passive receptors of particulate and dissolved organic carbon but locations where carbon is actively cycled, with implications for the understanding of carbon cycling and water treatment in peatland catchments.  相似文献   

18.
《Continental Shelf Research》2007,27(10-11):1584-1599
Historic data from the Russian-American Hydrochemical Atlas of Arctic Ocean together with data from the TRANSDRIFT II 1994 and TUNDRA 1994 cruises have been used to assess the spatial and inter-annual variability of carbon and nutrient fluxes, as well as air–sea CO2 exchange in the Laptev and western East Siberian Seas during the summer season. Budget computations using summer data of dissolved inorganic phosphate (DIP), dissolved inorganic nitrogen (DIN) and dissolved inorganic carbon (DIC) gives that the Laptev Sea shelf is a net sink of DIP and DIN of 2.5×106, 23.2×106 mol d−1, respectively, while it is a net source of DIC (excluding air–sea exchange) of 1249×106 mol d−1. In the East Siberian Seas the budget computations give 0.5×106, −11.4×106 and −173×106 mol d−1 (minus being a sink) for DIP, DIN, and DIC, respectively. In summers, the Laptev Sea Shelf is net autotrophic while the East-Siberian Sea Shelf is net heterotrophic, and both systems are weak net denitrifying. The Laptev Sea Shelf takes up 2.1 mmol CO2 m−2 d−1 from atmosphere, whereas the western part of the East-Siberian Sea Shelf loose 0.3 mmol CO2 m−2 d−1 to the atmosphere. The variability of DIP, DIN and DIC fluxes during summer in the different regions of the Laptev and East Siberian Seas depends on bottom topography, river runoff, exchange with surrounding seas and wind field.  相似文献   

19.
Lithological and hydrological influence on fluvial physical and chemical erosion was studied in a glacierized sedimentary basin with high evaporite presence. Suspended particulate matter (SPM), total dissolved solids (TDS) and major ion concentrations were analysed for 2 years of different hydrologic condition: (i) 2009–2010, Q = 100% average; and (ii) 2010–2011, Q = 60% average. Annual hydrograph was simple regime‐type with one peak in summer related to snow melting. The intra‐annual SPM and TDS variations were directly and inversely associated to Q, respectively. Snow chemistry showed continental influence (Na+/Ca2+ = 0.17), and atmospheric input of TDS was <1% of the total exported flux. River water was highly concentrated in Ca2+ and SO42− (~4 mmol l−1) and in Na+ and Cl− (~3 mmol l−1). Ca2+/SO42− and Na+/Cl− molar ratios were ~1 and related to Q, directly and inversely, respectively. Major ion relationships suggest that river chemistry is controlled by evaporite (gypsum and halite) dissolution having a summer input from sulfide oxidation and carbonate dissolution, and a winter input from subsurface flow loaded with silicate weathering products. This variation pattern resulted in nearly chemostatic behaviour for Ca+, Mg2+ and SO42−, whereas Na+, Cl− and SiO2 concentrations showed to be controlled by dilution/concentration processes. During the 2009–2010 hydrological year, the fluxes of water, SPM and TDS registered in the snow melting–high Q season were, respectively, 71%, 92% and 67% of the annual total, whereas for equal period in 2010–2011, 56% of water, 86% of SPM and 54% of TDS annual fluxes were registered. The SPM fluxes for 2009–2010 and 2010–2011 were 1.19 × 106 and 0.79 × 106 t year−1, whereas TDS fluxes were 0.68 × 106 and 0.55 × 106 t year−1, respectively. Export rates for 2009–2010 were 484 t km2 year−1 for SPM and 275 t km2 year−1 for TDS. These rates are higher than those observed in glacierized granite basins and in non‐glacierized evaporite basins, suggesting a synergistic effect of lithology and glaciers on physical and chemical erosion. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

20.
Seasonal suspended sediment transfer in glaciated catchments is responsive to meteorological, geomorphological, and glacio-fluvial conditions, and thus is a useful indicator of environmental system dynamics. Knowledge of multifaceted fluvial sediment-transfer processes is limited in the Alaskan Arctic – a region sensitive to contemporary environmental change. For two glaciated sub-catchments at Lake Peters, northeast Brooks Range, Alaska, we conducted a two-year endeavour to monitor the hydrology and meteorology, and used the data to derive multiple-regression models of suspended sediment load. Statistical selection of the best models shows that incorporating meteorological or temporal explanatory variables improves performances of turbidity- and discharge-based sediment models. The resulting modelled specific suspended sediment yields to Lake Peters are: 33 (20–60) t km−2 yr−1 in 2015, and 79 (50–140) t km−2 yr−1 in 2016 (95% confidence band estimates). In contrast to previous studies in Arctic Alaska, fluvial suspended sediment transfer to Lake Peters was primarily influenced by rainfall, and secondarily influenced by temperature-driven melt processes associated with clockwise diurnal hysteresis. Despite different sub-catchment glacier coverage, specific yields were the same order of magnitude from the two primary inflows to Lake Peters, which are Carnivore Creek (128 km2; 10% glacier coverage) and Chamberlin Creek (8 km2; 23% glacier coverage). Seasonal to longer-term sediment exhaustion and/or contrasting glacier dynamics may explain the lower than expected relative specific sediment yield from the more heavily glacierized Chamberlin Creek catchment. Absolute suspended sediment yield (t yr−1) from Carnivore Creek to Lake Peters was 27 times greater than from Chamberlin Creek, which we attribute to catchment size and sediment supply differences. Our results provide a foundational understanding of the current sediment transfer regime and are useful for predicting changes in fluvial sediment transport in glaciated Alaskan Arctic catchments.  相似文献   

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