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1.
Evaluating the role of fluvial transfer of terrestrial organic carbon (OC) and subsequent burial in the global carbon cycle requires the sources and fluxes of fluvial OC to be assessed, which remains poorly constrained in the Huanghe (Yellow River). Here, we report the elemental, stable isotopic, and radiocarbon activity of particulate organic carbon (POC) sampled at the outlet of Huanghe in 2012–2013. We show that the Huanghe riverine POC can be explained by binary mixing of fossil (POCfossil) and non‐fossil (POCnon‐fossil) components, the former may reach ~40% of the total POC. The Huanghe POCnon‐fossil is mostly sourced from C3 plants, with a mean residence time of c. 2200 years. The current human‐controlled hydrological regime strongly influenced the POC sources, transport modes, and fluxes. In 2012–2013, the Huanghe delivered 0.73 Tg (1 Tg = 1012 g) of POC to the sea, and about 28% of the annual POC flux occurred within a short human induced flood event. Globally, the Huanghe should be one of the largest rivers in the transfer and re‐burial of fossil OC. However, the fate of Huanghe fossil OC is still unconstrained and needs to be further investigated. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

2.
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   

3.
Total organic carbon fluxes of the Red River system (Vietnam)   总被引：1，自引：0，他引：1       下载免费PDF全文
Riverine transport of organic carbon from terrestrial ecosystems to the oceans plays an important role in the global carbon cycle. The Red River is located in Southeast Asia where river discharge, sediment loads and fluxes of elements (carbon, nitrogen and phosphorus) associated with suspended solids have been dramatically altered over past decades as a result of reservoir impoundment and land use, population, and climate change. Dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations were measured monthly at four stations of the Red River system from January 2008 to December 2010. The results reveal that POC changed synchronically with total suspended solids (TSS) concentration and with the river discharge, whereas no clear trend was observed for DOC concentration. The mean value of total organic carbon (TOC = DOC + POC) flux in the delta of the Red River was 31.5 × 1013 ± 4.0 × 1013 MgC.yr?1 (range 27.9–35.8 × 1013 MgC.yr?1 which leads to a specific TOC flux of 2012 ± 255 kgC.km?2.yr?1 during this 2008–2010 period. About 80% of the TOC flux was transferred to the estuary during the rainy season as a consequence of the higher river water discharge. The high mean value of the POC:Chl‐a ratio (1585 ± 870 mgC.mgChl‐a?1) and the moderate C:N ratio (7.3 ± 0.1) in the water column system suggest that organic carbon in the Red River system is mainly derived from erosion and soil leaching in the basin. The effect of two new dam impoundments in the Red River was also observable with lower TOC fluxes in 2010 compared with 2008. Copyright © 2017 John Wiley & Sons, Ltd.  相似文献   

4.
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   

5.
Riverine total suspended sediment (TSS) at the lower reach section of the Zengjiang River, a low‐turbidity river in the southern China, was sampled on a 4‐week basis from March 2002 to February 2003. The gross TSS was divided into sedimentary and suspended fractions (SED and SUS) by the sedimentation method. Organic carbon and nitrogen, 14C and 13C were analysed using an elemental analyser and accelerator mass spectrometer respectively. The results show that particulate organic carbon (POC) yield is 0·8 × 106 g km?2 year?1 in the Zengjiang River drainage basin, which is about one‐tenth of that in the Zhujiang (Pearl) River drainage basin. The C/N ratio demonstrates that aquatic biomass is the major contributor to POC in the Zengjiang River. The average share of aquatic biomass in the SUS‐fraction POC and SED‐fraction POC is about 88·89% and 62·76% respectively, with a substantial seasonal variation. δ13C values of SUS‐fraction POC (?26·56 to ? 22·89‰) is slightly lighter than that of SED‐fraction POC (?25·05 to ? 22·20‰), indicating that the contribution of aquatic biomass to δ13C values is more pronounced in the SUS‐fraction POC than in the SED‐fraction POC. The ‘bomb’–14C signature is not detected in the POC of Zengjiang River, and the contribution from geological organic carbon is very little. Δ14C values of the SED‐fraction POC vary from ? 44 to ? 223‰, and the Δ14C values of the SUS‐fraction POC vary from ? 33 to ? 165‰. For most paired samples, the SED‐fraction POC is generally more depleted in 14C than that of its counterpart SUS‐fraction POC. Compared with other small mountainous rivers, the 14C enrichment of POC in the Zengjiang River indicates slight drainage basin erosion. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

6.
In situ measurement of grain‐scale fluvial morphology is important for studies on grain roughness, sediment transport and the interactions between animals and the geomorphology, topics relevant to many river practitioners. Close‐range digital photogrammetry (CRDP) and terrestrial laser scanning (TLS) are the two most common techniques to obtain high‐resolution digital elevation models (DEMs) from fluvial surfaces. However, field application of topography remote sensing at the grain scale is presently hindered mainly by the tedious workflow challenges that one needs to overcome to obtain high‐accuracy elevation data. A recommended approach for CRDP to collect high‐resolution and high‐accuracy DEMs has been developed for gravel‐bed flume studies. The present paper investigates the deployment of the laboratory technique on three exposed gravel bars in a natural river environment. In contrast to other approaches, having the calibration carried out in the laboratory removes the need for independently surveyed ground‐control targets, and makes for an efficient and effective data collection in the field. Optimization of the gravel‐bed imagery helps DEM collection, without being impacted by variable lighting conditions. The benefit of a light‐weight three‐dimensional printed gravel‐bed model for DEM quality assessment is shown, and confirms the reliability of grain roughness data measured with CRDP. Imagery and DEM analysis evidences sedimentological contrasts between gravel bars within the reach. The analysis of the surface elevations shows the effect variable grain‐size and sediment sorting have on the surface roughness. By plotting the two‐dimensional structure functions and surface slopes and aspects we identify different grain arrangements and surface structures. The calculation of the inclination index allows determining the surface‐forming flow direction(s). We show that progress in topography remote sensing is important to extend our knowledge on fluvial morphology processes at the grain scale, and how a technique customized for use by fluvial geomorphologists in the field benefits this progress. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

7.
Global peatlands store an unparalleled proportion of total global organic carbon but it is vulnerable to erosion into fluvial systems. Fluvial networks are being recognized as areas of carbon transformation, with eroded particulate organic carbon processed to dissolved organic carbon and CO2. Existing studies indicate biodegradation and photodegradation as key processes controlling the transformation of organic carbon in fluvial systems, with initial concentrations of dissolved organic carbon (DOC) identified as a control on the rate of carbon mineralization. This study manipulates temperature and incident light intensity to investigate carbon mineralization rates in laboratory simulations of peatland sediment transport into fluvial systems. By directly measuring gaseous CO2 emissions from sampled stream water, the relationship of temperature and light intensity with carbon efflux is identified. In simulations where sediment (as particulate organic matter, POM) is absent, temperature is consistently the dominant factor influencing carbon efflux rates. This influence is independent of the initial DOC concentration of the water sample. In simulations where POM was added, representing a peatland river receiving eroded terrestrial sediment, initial DOC concentration predicts 79% of the variation in total gaseous carbon efflux whereas temperature and light intensity predict 12% and 3%, respectively. When sampled stream water's mineralization rates in the presence of added POM are analysed independently, removing DOC as a model variable, the dominant variable affecting CO2 efflux is opposite for each sample. This study presents novel data suggesting peatland erosion introduces further complexity to dynamic stream systems where rates of carbon transformation processes and the influence of specific environmental variables are interdependent. Anthropogenic climate change is identified as a leading risk factor perpetuating peatland erosion; therefore, understanding the fate of terrestrial sediment in rivers and further quantifying the benefits of protecting peatland soils will be of increasing importance to carbon budgeting and ecosystem function studies.  相似文献   

8.
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 (POCL), 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 POCL was 9.9 g C m‐2 y‐1 with highest values observed for semi‐arid soils (POCL = 10.8 g C m‐2 y‐1), followed by tropical soils (POCL = 6.4 g C m‐2 y‐1) and temperate soils (POCL = 1.7 g C m‐2 y‐1). Considering the mean POCL 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.  相似文献   

9.
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 δ13CDOC values made it possible to link exported DOC with its within‐bog source, δ18OH2O 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 δ13CDOC 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.  相似文献   

10.
We investigate sources of both dissolved and particulate organic carbon in the St Lawrence River from its source (the Great Lakes outlet) to its estuary, as well as in two of its tributaries. Special attention is given to seasonal interannual patterns by using data collected on a bi‐monthly basis from mid‐1998 to mid‐2003. δ13C measurements in dissolved inorganic carbon, dissolved organic carbon (DOC) and particulate organic carbon (POC), as well as molar C : N in particulate organic matter (POM), are used to bring insight into the dynamic between aquatic versus terrigenous sources. In addition, 14C activities of DOC were measured at the outlet of the St Lawrence River to its estuary to assess a mean age of the DOC exported to the estuary. In the St Lawrence River itself, aquatically produced POC dominates terrestrially derived POC and is depleted in 13C by approximately 12‰ versus dissolved CO2. In the Ottawa River, the St Lawrence River's most important tributary, the present dataset did not allow for convincing deciphering of POC sources. In a small tributary of the St Lawrence River, aquatically produced POC dominates in summer and terrestrially derived POC dominates in winter. DOC seems to be dominated by terrestrially derived organic matter at all sampling sites, with some influence of DOC derived from aquatically produced POC in summer in the St Lawrence River at the outlet of the Great Lakes and in one of its small tributaries. The overall bulk DOC is relatively recent (14C generally exceeding 100% modern carbon) in the St Lawrence River at its outlet to the estuary, suggesting that it derives mainly from recent organic matter from topsoils in the watershed. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

11.
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   

12.
Time‐lapse seismic analysis is utilized in CO2 geosequestration to verify the CO2 containment within a reservoir. A major risk associated with geosequestration is a possible leakage of CO2 from the storage formation into overlaying formations. To mitigate this risk, the deployment of carbon capture and storage projects requires fast and reliable detection of relatively small volumes of CO2 outside the storage formation. To do this, it is necessary to predict typical seepage scenarios and improve subsurface seepage detection methods. In this work we present a technique for CO2 monitoring based on the detection of diffracted waves in time‐lapse seismic data. In the case of CO2 seepage, the migrating plume might form small secondary accumulations that would produce diffracted, rather than reflected waves. From time‐lapse data analysis, we are able to separate the diffracted waves from the predominant reflections in order to image the small CO2 plumes. To explore possibilities to detect relatively small amounts of CO2, we performed synthetic time‐lapse seismic modelling based on the Cooperative Research Centre for Greenhouse Gas Technologies (CO2CRC) Otway project data. The detection method is based on defining the CO2 location by measuring the coherency of the signal along diffraction offset‐traveltime curves. The technique is applied to a time‐lapse stacked section using a stacking velocity to construct offset‐traveltime curves. Given the amount of noise found in the surface seismic data, the predicted minimum detectable amount of CO2 is 1000–2000 tonnes. This method was also applied to real data obtained from a time‐lapse seismic physical model. The use of diffractions rather than reflections for monitoring small amounts of CO2 can enhance the capability of subsurface monitoring in CO2 geosequestration projects.  相似文献   

13.
Peatlands cover a very small area of the Earth, but store globally significant quantities of carbon and export disproportionate quantities of fluvial organic carbon, especially when the peatlands are degraded or disturbed. Peatland headwater catchments with high concentrations of dissolved and particulate organic carbon (DOC and POC) provide an opportunity to investigate the possibility of competing effects that could lead to enhanced or diminished turnover of DOC in the presence of POC. Both POC and DOC can be degraded by light and microbes, producing smaller molecules and releasing CO2 and CH4 to the atmosphere, and POC can inhibit light penetration, stabilize DOC by providing adsorption sites and providing surfaces for microbes to interact with DOC. However, the majority of peatland fluvial carbon studies are conducted using filtered water samples, and measure only the DOC concentration, so the impact of the particulate organic matter (POM) on in-stream processing of organic carbon is relatively unknown. It is therefore possible that studies have underestimated carbon transformations in rivers as they have not considered the interaction of the particulate material on the dissolved concentrations; there could be higher losses than previously estimated, increasing the contribution of peatland headwaters to GHG emissions. In this study, we assessed if the current approach of DOC degradation studies accurately represent the impact of POM on DOC degradation, by quantifying DOC production from POM, and therefore POC, over time in water with manipulated POM concentrations. Both filtered and unfiltered water lost 60% of the DOC over 70 hours, whereas the treatment with additional POM lost only 35%. The results showed that filtering does not significantly impact the DOC degradation rates; however, when the POC concentration was doubled, there was a significant reduction in DOC degradation, suggesting that filtering would still be necessary to get accurate rates of DOC transformations in waters with high POC concentrations.  相似文献   

14.
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.  相似文献   

15.
Rivers are dynamic components of the terrestrial carbon cycle and provide important functions in ecosystem processes. Although rivers act as conveyers of carbon to the oceans, rivers also retain carbon within riparian ecosystems along floodplains, with potential for long‐term (> 102 years) storage. Research in ecosystem processing emphasizes the importance of organic carbon (OC) in river systems, and estimates of OC fluxes in terrestrial freshwater systems indicate that a significant portion of terrestrial carbon is stored within river networks. Studies have examined soil OC on floodplains, but research that examines the potential mechanistic controls on OC storage in riparian ecosystems and floodplains is more limited. We emphasize three primary OC reservoirs within fluvial systems: (1) standing riparian biomass; (2) dead biomass as large wood (LW) in the stream and on the floodplain; (3) OC on and beneath the floodplain surface, including litter, humus, and soil organic carbon (SOC). This review focuses on studies that have framed research questions and results in the context of OC retention, accumulation and storage within the three primary pools along riparian ecosystems. In this paper, we (i) discuss the various reservoirs for OC storage in riparian ecosystems, (ii) discuss physical conditions that facilitate carbon retention and storage in riparian ecosystems, (iii) provide a synthesis of published OC storage in riparian ecosystems, (iv) present a conceptual model of the conditions that favor OC storage in riparian ecosystems, (v) briefly discuss human impacts on OC storage in riparian ecosystems, and (vi) highlight current knowledge gaps. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

16.
This study uses long‐term records of stream chemistry, discharge and air temperature from two neighbouring forested catchments in the southern Appalachians in order to calculate production of dissolved CO2 and dissolved inorganic carbon (DIC). One of the pair of catchments was clear‐felled during the period of the study. The study shows that: (1) areal production rates of both dissolved CO2 and DIC are similar between the two catchments even during and immediately after the period of clear‐felling; (2) flux of total inorganic carbon (dissolved CO2+ DIC) rises dramatically in response to a catchment‐wide acidification event; (3) DIC and dissolved CO2 are dominantly released on the old water portion of the discharge and concentrations peak in the early autumn when flows in the study catchments are at their lowest; (4) total fluvial carbon flux from the clear‐felled catchment is 11·6 t km−2 year−1 and for the control catchment is 11·4 t km−2 year−1. The total inorganic carbon flux represents 69% of the total fluvial carbon flux. The method presented in the study provides a useful way of estimating inorganic carbon flux from a catchment without detailed gas monitoring. The time series of dissolved CO2 at emergence to the stream can also be a proxy for the soil flux of CO2. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

17.
The Yellow River transports a large amount of sediment and particulate organic carbon (POC), which is thought to mainly derive from erosion of the Chinese Loess Plateau (CLP). However, the compositions, sources and erosional fluxes of POC in the Yellow River remain poorly constrained. Here we combined measurements of mineralogy, total organic carbon content (OCtotal), stable organic carbon isotopes (δ13Corg), radiocarbon (14C) activity of organic matter in bulk suspended sediments collected seasonally from the upper and middle Yellow River, to quantify the compositions and fluxes of the POC and to assess its sources (biospheric and petrogenic POC, i.e. POCbio and POCpetro, respectively). The results showed that the POC loading of sediments was controlled by mineralogy, grain size and specific surface area of loess particles. The Fmod of POC (0.71 to 0.31) can be explained by mixing of POCpetro with modern and aged POCbio. A binary mixing model based on the hyperbolic relationship of the Fmod and OCtotal revealed a wide range of ages of POCbio from 1300 to 11100 14C years. Relative to the upstream station, the annual POCbio and POCpetro fluxes in the Yellow River are more than doubled after it flows crossing the CLP within 35% drainage area gain, resulting in POCbio and POCpetro yields of the CLP at 3.50 ± 0.59 and 0.48 ± 0.49 tC/km2/yr, respectively. POC flux seasonal variation revealed that monsoon rainfall exerts a first-order control on the export of both POCbio and POCpetro from the CLP to the Yellow River, resulting in more than 90% of the annual POC exported during the monsoon season. Around one third of annual POC erosional flux was transported during a storm event period, highlighting the important role of extreme events in POC export in this large river. © 2020 John Wiley & Sons, Ltd.  相似文献   

18.
Stream bathymetry is a critical variable in a number of river science applications. In larger rivers, bathymetry can be measured with instruments such as sonar (single or multi‐beam), bathymetric airborne LiDAR (light detection and ranging), or acoustic Doppler current profilers. However, in smaller streams with depths less than 2 m, bathymetry is one of the more difficult variables to map at high‐resolution. Optical remote sensing techniques offer several potential solutions for collecting high‐resolution bathymetry. In this research, I focus on direct photogrammetric measurements of bathymetry using multi‐view stereo photogrammetry, specifically Structure‐from‐Motion (SfM). The main barrier to accurate bathymetric mapping with any photogrammetric technique is correcting for the refraction of light as it passes between the two different media (air and water), which causes water depths to appear shallower than they are. I propose and test an iterative approach that calculates a series of refraction correction equations for every point/camera combination in a SfM point cloud. This new method is meant to address shortcomings of other correction techniques and works within the current preferred method for SfM data collection, oblique and highly convergent photographs. The multi‐camera refraction correction presented here produces bathymetric datasets with accuracies of ~0.02% of the flying height and precisions of ~0.1% of the flying height. This methodology, like many fluvial remote sensing methods, will only work under ideal conditions (e.g. clear water), but it provides an additional tool for collecting high‐resolution bathymetric datasets for a variety of river, coastal, and estuary systems. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

19.
The grain‐scale morphology of fluvial sediments is an important control on the character and dynamics of river systems; however current understanding of its role is limited by the difficulties of robustly quantifying field surface morphology. Terrestrial Laser Scanning (TLS) offers a new methodology for the rapid acquisition of high‐resolution and high‐precision surface elevation data from in situ sediments. To date, most environmental and fluvial applications of TLS have focused on large‐scale systems, capturing macroscale morphologies. Application of this new technology at scales necessary to characterize the complexity of grain‐scale fluvial sediments therefore requires a robust assessment of the quality and sources of errors in close‐range TLS data. This paper describes both laboratory and field experiments designed to evaluate close‐range TLS for sedimentological applications and to develop protocols for data acquisition. In the former, controlled experiments comprising high‐resolution scans of white, grey and black planes and a sphere were used to quantify the magnitude and source of three‐dimensional (3D) point errors resulting from a combination of surface geometry, reflectivity effects and inherent instrument precision. Subsequently, a methodology for the collection and processing of grain‐scale TLS data is described through an application to a coarse grained gravel system, the River Feshie (D50 32 to 63 mm). This stepwise strategy incorporates averaging repeat scans and filtering scan artefact and non‐surface points using local 3D search algorithms. The sensitivity of the results to the filter parameter values are assessed by careful internal validation of Digital Terrain Models (DTMs) created from the resulting point cloud data. The transferability of this methodology is assessed through application to a second river, Bury Green Brook, dominated by finer gravel (D50 18 to 33 mm). The factor limiting the resolution of DTMs created from this second dataset was found to be the relative sizes of the laser footprint and smallest grains. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

20.
Carbon transported by rivers is an important component of the global carbon cycle. Here, we report on organic carbon transport along the third largest river in China, the Songhua River, and its major tributaries. Water samples were collected seasonally or more frequently to determine dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations and C/N and stable carbon isotopic ratios. Principal component analysis and multiple regression analysis of these data, in combination with hydrological records for the past 50 years, were used to determine the major factors influencing the riverine carbon fluxes. Results indicate that the organic carbon in the Songhua River basin is derived mainly from terrestrial sources. In the 2008–2009 hydrological year, the mean concentrations of DOC and POC were 5.87 and 2.36 mg/L, and the estimated fluxes of the DOC and POC were 0.30 and 0.14 t·km?2·year?1, respectively. The riverine POC and DOC concentrations were higher in subcatchments with more cropland, but the area‐specific fluxes were lower, owing to decreased discharge. We found that hydrological characteristics and land‐use type (whether forest or cropland) were the most important factors influencing carbon transport in this system. Agricultural activity, particularly irrigation, is the principal cause of changes in water discharge and carbon export. Over the last 50 years, the conversion of forest to cropland has reduced riverine carbon exports mainly through an associated decrease in discharge following increased extraction of water for irrigation.  相似文献   

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