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1.
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   

2.
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   

3.
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   

4.
The fluvial flux of carbon (C) from terrestrial to marine environments represents an important component of the global C‐cycle, which can transfer C from the atmosphere to sedimentary storage. Fluvial fluxes of C are also an essential resource for freshwater ecosystems, critical for habitat heterogeneity and function. As such it is crucial that we are able to quantify this flux accurately. However, at present there are a number of different techniques used to quantify concentrations of fluvial C, and these techniques vary in their accuracy. In this article, we compare particulate organic carbon (POC) measurements derived from two commonly‐used techniques; a simple combustion and loss‐on‐ignition (LOI) technique, and an oxidative–combustion and carbon dioxide (CO2) detection technique. The techniques were applied to water samples collected from 10 contrasting reference‐condition, temperate river ecosystems. The POC measurements derived from the LOI technique were up to 16 times higher (average four times higher), than those derived from the oxidative–combustion and CO2 detection technique. This difference was highly variable both across the different river ecosystems and within each river ecosystem over time, suggesting that there is no simple way of converting the mass measured by LOI to estimates of fluvial POC. It is suggested that the difference in POC measured by these two techniques is a consequence of: (1) the loss of inorganic carbon at LOI combustion temperatures of > 425 °C, (2) the potential during the LOI combustion stage to lose hygroscopic and intercrystalline water, not completely driven off by the drying stage at temperatures of < 150 °C, and (3) the variable C content of fluvial organic matter, meaning that the simple application of a fixed correction factor to values obtained from the LOI technique may not be appropriate. These findings suggest that oxidative–combustion and CO2 detection techniques are preferential for quantifying fluvial POC. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

5.
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   

6.
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   

7.
Arctic glaciers are rapidly responding to global warming by releasing organic carbon (OC) to downstream ecosystems. The glacier surface is arguably the most biologically active and biodiverse glacial habitat and therefore the site of important OC transformation and storage, although rates and magnitudes are poorly constrained. In this paper, we present measurements of OC fluxes associated with atmospheric deposition, ice melt, biological growth, fluvial transport and storage (in superimposed ice and cryoconite debris) for a supraglacial catchment on Foxfonna glacier, Svalbard (Norway), across two consecutive years. We found that in general atmospheric OC input (averaging 0.63 ± 0.25 Mg a-1 total organic carbon, i.e. TOC, and 0.40 ± 0.22 Mg a-1 dissolved organic carbon, i.e. DOC) exceeded fluvial OC export (0.46 ± 0.04 Mg a-1 TOC and 0.36 ± 0.03 Mg a-1 DOC). Early in the summer, OC was mobilised in snowmelt but its release was delayed by temporary storage in superimposed ice on the glacier surface. This delayed the export of 28.5% of the TOC in runoff. Biological production in cryoconite deposits was a negligible potential source of OC to runoff, while englacial ice melt was far more important on account of the glacier's negative ice mass balance (–0.89 and –0.42 m a-1 in 2011 and 2012, respectively). However, construction of a detailed OC budget using these fluxes shows an excess of inputs over outputs, resulting in a net retention of OC on the glacier surface at a rate that would require c. 3 years to account for the OC stored as cryoconite debris. © 2018 John Wiley & Sons, Ltd.  相似文献   

8.
Rivers of South and Southeast Asia disgorge large suspended sediment loads, reflecting exceptionally high rates of erosion promoted by natural processes (tectonic and climatic) and anthropogenic (land‐use change) activities that are characteristic of the region. While particulate carbon and nitrogen fluxes have been characterized in some large Asian rivers, less is known about the headwater systems where much sediment and organic material are initially mobilized. This study, conducted in the 74‐km2 Mae Sa Experimental Catchment in northern Thailand, shows that the Sa River is an important source for particulate organic carbon (POC) and particulate organic nitrogen (PON) transported to larger river systems and downstream reservoirs. However, the yields during three years of investigation varied greatly: 5.0–22.3 Mg POC km?2 y?1 and 0.48–2.02 Mg PON km?2 y?1. The 22.3 Mg POC km?2 y?1 yield is the highest reported for any river on the Asian continent. Stream samples collected during 12 storms showed that almost 3% of the total suspended solid load is POC 0.7 µm to 2.0 mm in size. This percentage is higher than other values for most large rivers on the continent. Further, we documented a strong pulse hysteretic behaviour in the stream, whereby peak fluxes of POC and PON are often delayed (anticlockwise hysteresis) or accelerated (clockwise hysteresis) relative to stream flow peaks (or are complex), complicating the prediction of storm‐based or annual particulate carbon and nitrogen fluxes. Stream turbidity and total suspended sediment are reasonable proxies for POC and PON concentrations, while stream discharge is not a good predictor variable. Observed C:N ratios for measured particulate samples range from 3 to 83, with the high‐end values likely associated with fresh (non‐decomposed) vegetative material greater than 2 mm in diameter. The C:N ratio (weighted based on three sediment sizes) for 12 events ranges from 7.5 to 15.3. These modest values reflect the relatively low C:N ratios for small size fractions (0.7–0.63 µm) that comprise 50–90% of the TSS load in the events. Overall, organic material <0.63 µm contribute about 75% of the total POC load and 80% of the PON load. The annual C:N ratio for the river is approximately 10–11. Collectively, our findings indicate the occasionally high yields make the Sa River—and potentially other similar headwater rivers—a hot spot for POC and PON transported to downstream water bodies. Complex hysteresis patterns and high year‐to‐year variability hinders our ability to calculate and predict these yields without continuous, automated monitoring of discharge and turbidity. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

9.
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   

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.
The present contribution focuses on modeling the total particulate organic carbon (POC) and benthic POC transport from a lowland stream impacted by agricultural land‐use. A mass balance, reach scale model is verified that accounts for water, sediment and POC transport, sediment and POC temporary storage and exchange with the streambed, and production and degradation of carbon pools in the benthos. We found that the POC load is highly variable during individual hydrologic events and is influenced by transport of mixed carbon sources including upland, streambank and benthic POC sources. Benthic POC stocks and transport were found to vary seasonally and annually but are in a state of long‐term equilibrium. Equilibrium is governed by negative feedback mechanisms whereby high POC export due to extreme hydrologic events and high‐frequency hydrologic events reduces benthic POC stocks and inhibits benthic POC growth. Benthic POC accounted for 4 tC y?1 or 22% of the total annual POC loading in the stream's main stem and 8.9 tC y?1 or 48% of the POC yield for the entire watershed. These results suggest that further attention should be given to benthic‐derived POC when budgeting stream ecosystem carbon for low‐order stream systems. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

12.
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 (POCL and DOCL). 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 (TOCL) were incurred mainly in particulate form (~94%) and the increase in TOCL 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 TOCL 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.  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.
在博斯腾湖选取了13个点位,于2012年5、8、10月测定表层和底层水体中的颗粒有机碳、溶解有机碳、颗粒有机氮和叶绿素a含量.结果显示颗粒和溶解有机碳在表层水体中的浓度与底层相近.博斯腾湖水体中颗粒有机碳的季节变化十分明显,其平均浓度从春季(0.64 mg/L)到夏季(0.71 mg/L)变化不大,但在秋季变化十分显著(浓度达1.58 mg/L).其中西北湖区和湖心区颗粒有机碳的季节变化最明显,东部湖区颗粒有机碳的季节变化相对较小.博斯腾湖水体的颗粒有机碳在春、秋两季主要来自外源输入,在夏季受水体中浮游生物的影响较大.博斯腾湖水体中溶解有机碳也具有一定的季节变化,夏季浓度(平均为9.3 mg/L)略低于春、秋两季(平均为10.3 mg/L).溶解有机碳在河口区的季节变化最强,其夏季浓度明显偏低,主要是由于开都河河水的稀释作用.总体上,博斯腾湖水体中溶解有机碳浓度的变化主要受外部因素的影响.  相似文献   

16.
湖泊沉积物有机碳埋藏是陆地碳循环中重要的环节,对全球碳平衡起着重要的作用.洱海是云贵高原第二大淡水湖,目前对洱海生态环境变化、重金属与营养盐污染等已展开了较为深入的研究,但对近百年来沉积物有机碳埋藏时空变化与驱动因素缺乏系统的分析.本文通过对洱海北部湖区典型岩芯（编号EH2012）以及其他湖区13个沉积岩芯中有机碳（OC）含量的分析,结合湖泊生态环境与气候因子变化,研究了近百年来沉积物有机碳埋藏时空变化特征与影响因素.C/N摩尔比值表明洱海沉积物中OC以湖泊内源为主,不同湖区岩芯中OC含量变化趋势基本相似.以EH2012岩芯为例,OC含量历史变化可分为3个阶段：1970年以前,表现出较稳定的低值;1970-2000年,OC含量逐渐增加;2000年以来,OC含量增加更加明显并达到近百年来的最大值.近百年来,EH2012岩芯有机碳累积速率（OCAR）呈逐渐增加趋势,变化范围为7.9~87.2 g/（m2·a）,平均OCAR（OCAR）为24.1 g/（m2·a）;OCAR变化与OC含量和区域气温呈显著正相关,全球变暖与营养驱动下的湖泊生产力提高可能是近年来OCAR增加的主要原因之一.基于重金属Cd污染初始时间建立的时标,1982年以来不同湖区OCAR为17.1~44.7 g/（m2·a）,采用克里金插值得到的全湖OCAR均值为31.4 g/（m2·a）;不同湖区OCAR与磷累积速率呈显著正相关,指示了湖泊营养水平对有机碳埋藏空间变化的重要影响.  相似文献   

17.
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   

18.
A key issue in the study of the carbon cycle is constraining the stocks and fluxes in and between C‐reservoirs. Among these, the role and importance of fossil organic carbon (FOC) release by weathering of outcropping sedimentary rocks on continental surfaces is still debated and remains poorly constrained. Our work focuses on FOC fluxes due to chemical and mechanical weathering of marls in two experimental watersheds with typical badlands geomorphology (Draix watersheds, Laval and Moulin, Alpes de Haute Provence, France). Organic matter from bedrock, soil litter and riverine particles are characterized by Rock‐Eval 6 pyrolysis. FOC fluxes due to mechanical weathering are then estimated by monitoring the annual particulate solid exports at the outlets of the watersheds (1985–2005 period). FOC fluxes from chemical weathering were calculated using Ca2+ concentrations in dissolved loads (year 2002) to assess the amount of FOC released by the dissolution of the carbonate matrix. Results show that FOC delivery is mainly driven by mechanical weathering, with a yield ranging from 30 to 59 t km‐2 yr‐1 in the Moulin (0.08 km2) and Laval (0.86 km2) catchments, respectively, (1985–2005 average). The release of FOC attributed to chemical weathering was 2.2 to 4.2 t km‐2 for the year 2002. These high FOC fluxes from badlands are similar to those observed in tectonically active mountain catchments. At a regional scale, badland outcropping within the Durance watershed does not exceed 0.25% in area of the Rhône catchment, but could annually deliver 12 000 t yr‐1 of FOC. This flux could correspond to 27% of the total particulate organic carbon (POC) load exported by the Rhône River to the Mediterranean Sea. At a global scale, our findings suggest that erosion of badlands may contribute significantly to the transfer of FOC from continental surfaces to depositional environments. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

19.
The China Seas include the South China Sea, East China Sea, Yellow Sea, and Bohai Sea. Located off the Northwestern Pacific margin, covering 4700000 km~2 from tropical to northern temperate zones, and including a variety of continental margins/basins and depths, the China Seas provide typical cases for carbon budget studies. The South China Sea being a deep basin and part of the Western Pacific Warm Pool is characterized by oceanic features; the East China Sea with a wide continental shelf, enormous terrestrial discharges and open margins to the West Pacific, is featured by strong cross-shelf materials transport; the Yellow Sea is featured by the confluence of cold and warm waters; and the Bohai Sea is a shallow semiclosed gulf with strong impacts of human activities. Three large rivers, the Yangtze River, Yellow River, and Pearl River, flow into the East China Sea, the Bohai Sea, and the South China Sea, respectively. The Kuroshio Current at the outer margin of the Chinese continental shelf is one of the two major western boundary currents of the world oceans and its strength and position directly affect the regional climate of China. These characteristics make the China Seas a typical case of marginal seas to study carbon storage and fluxes. This paper systematically analyzes the literature data on the carbon pools and fluxes of the Bohai Sea,Yellow Sea, East China Sea, and South China Sea, including different interfaces(land-sea, sea-air, sediment-water, and marginal sea-open ocean) and different ecosystems(mangroves, wetland, seagrass beds, macroalgae mariculture, coral reefs, euphotic zones, and water column). Among the four seas, the Bohai Sea and South China Sea are acting as CO_2 sources, releasing about0.22 and 13.86–33.60 Tg C yr~(-1) into the atmosphere, respectively, whereas the Yellow Sea and East China Sea are acting as carbon sinks, absorbing about 1.15 and 6.92–23.30 Tg C yr~(-1) of atmospheric CO_2, respectively. Overall, if only the CO_2 exchange at the sea-air interface is considered, the Chinese marginal seas appear to be a source of atmospheric CO_2, with a net release of 6.01–9.33 Tg C yr~(-1), mainly from the inputs of rivers and adjacent oceans. The riverine dissolved inorganic carbon (DIC) input into the Bohai Sea and Yellow Sea, East China Sea, and South China Sea are 5.04, 14.60, and 40.14 Tg C yr~(-1),respectively. The DIC input from adjacent oceans is as high as 144.81 Tg C yr~(-1), significantly exceeding the carbon released from the seas to the atmosphere. In terms of output, the depositional fluxes of organic carbon in the Bohai Sea, Yellow Sea, East China Sea, and South China Sea are 2.00, 3.60, 7.40, and 5.92 Tg C yr~(-1), respectively. The fluxes of organic carbon from the East China Sea and South China Sea to the adjacent oceans are 15.25–36.70 and 43.93 Tg C yr~(-1), respectively. The annual carbon storage of mangroves, wetlands, and seagrass in Chinese coastal waters is 0.36–1.75 Tg C yr~(-1), with a dissolved organic carbon(DOC) output from seagrass beds of up to 0.59 Tg C yr~(-1). Removable organic carbon flux by Chinese macroalgae mariculture account for 0.68 Tg C yr~(-1) and the associated POC depositional and DOC releasing fluxes are 0.14 and 0.82 Tg C yr~(-1), respectively. Thus, in total, the annual output of organic carbon, which is mainly DOC, in the China Seas is 81.72–104.56 Tg C yr~(-1). The DOC efflux from the East China Sea to the adjacent oceans is 15.00–35.00 Tg C yr~(-1). The DOC efflux from the South China Sea is 31.39 Tg C yr~(-1). Although the marginal China Seas seem to be a source of atmospheric CO_2 based on the CO_2 flux at the sea-air interface, the combined effects of the riverine input in the area, oceanic input, depositional export,and microbial carbon pump(DOC conversion and output) indicate that the China Seas represent an important carbon storage area.  相似文献   

20.
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.  相似文献   

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