亚热带河口区水库DOC和DIC浓度时空变化特征

沿海水库汇聚并埋藏着大量的碳,是全球碳循环的重要区域.水体溶解有机碳(DOC)和溶解无机碳(DIC)的生物地球化学行为是水库碳循环研究的重要组成部分,对其系统生物过程和生态环境变化具有重要的影响.为了解亚热带河口区文武砂水库表层水体DOC和DIC的时空分布特征,本研究于2018年11月、2019年3月和6月分别对库区表层水进行多空间点位采样分析.结果表明,研究期间,文武砂水库表层水体DOC和DIC浓度变化范围分别介于0.10～21.13和0.38～34.94 mg/L,其均值分别为(4.09±0.18)和(15.83±0.24) mg/L,最大值分别出现在夏季和秋季;空间分布趋势,整体表现为北库区南库区,且由库区周边的浅水区向库区中心的深水区域呈现出递减的趋势;浮游植物光合作用强度是影响库区DOC和DIC浓度的季节变化的重要因素,而外源污染输入强度是引起库区DOC和DIC浓度空间变化的重要因素.本文结果扩展对水库碳循环的认知,对提高水库水质也提供了有益参考.     

Organic carbon transport in the Songhua River,NE China: Influence of land use

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.     

The impact of ditch blocking on fluvial carbon export from a UK blanket bog

We investigated the effects of ditch blocking on fluvial carbon concentrations and fluxes at a 5‐year, replicated, control‐intervention field experiment on a blanket peatland in North Wales, UK. The site was hydrologically instrumented, and run‐off via open and blocked ditches was analysed for dissolved organic carbon (DOC), particulate organic carbon, dissolved carbon dioxide, and dissolved methane. DOC was also analysed in peat porewater and overland flow. The hillslope experiment was embedded within a paired control‐intervention catchment study, with 3 years of preblocking and 6 years of postblocking data. Results from the hillslope showed large reductions in discharge via blocked ditches, with water partly redirected into hillslope surface and subsurface flows, and partly into remaining open ditches. We observed no impacts of ditch blocking on DOC, particulate organic carbon, dissolved carbon dioxide or methane in ditch waters, DOC in porewaters or overland flow, or stream water DOC at the paired catchment scale. Similar DOC concentrations in ditch water, overland flow, and porewater suggest that diverting flow from the ditch network to surface or subsurface flow had a limited impact on concentrations or fluxes of DOC entering the stream network. The subdued response of fluvial carbon to ditch blocking in our study may be attributable to the relatively low susceptibility of blanket peatlands to drainage, or to physical alterations of the peat since drainage. We conclude that ditch blocking cannot be always be expected to deliver reductions in fluvial carbon loss, or improvements in the quality of drinking water supplies.     

The Bioavailability of Dissolved,Particulate, and Adsorbed Organic Carbon in Groundwater Systems

Dissolved organic carbon (DOC) is the smallest amount of organic carbon present in aquifer systems and is typically dwarfed by amounts of particulate organic carbon (POC) and adsorbed organic carbon (AOC). Research conducted over the last half century, however, has shown that these dissolved, particulate, and adsorbed compartments interact dynamically with each other. That suggests the hypothesis that the bioavailability of DOC in groundwater may indicate the bioavailability of the associated POC and AOC compartments as well. If that proves to be the case, it would greatly simplify the process of evaluating the bioavailability of total organic carbon present in groundwater systems. That hypothesis was examined by (1) comparing DOC bioavailability between two aquifers receiving modern atmospheric recharge, but with the recharge passing through POC/AOC sources of substantially different geologic ages, and (2) measuring POC/AOC bioavailability in sediments in from two aquifers before and after injection with bioavailable DOC consisting of dissolved sugars and emulsified vegetable oil. The results of both comparisons are consistent with the hypothesis that DOC bioavailability in groundwater reflects the bioavailability of the associated POC and AOC compartments and vice versa. Thus, DOC bioavailability may be a useful indicator of an aquifer's potential to drive reduction/oxidation processes that affect the chemical quality of groundwater.     

Fluvial organic carbon composition and concentration variability within a peatland catchment—Implications for carbon cycling and water treatment

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.     

Temporal and spatial characteristics of dissolved organic carbon in the Wujiang River,Southwest China

River systems play an important role in the global carbon cycle. Rivers transport carbon to the ocean and also affect the carbon cycle in the coastal ocean. The flux from land to the ocean is thought to be a very important part of the land carbon budget. To investigate the effect of dam-building on dissolved organic carbon(DOC)in rivers, three reservoirs of different trophic states in the Wujiang basin, Guizhou Province, were sampled twice per month between May 2011 and May 2012. Temporal and spatial distributions of DOC in the reservoirs and their released waters were studied. It was found that different factors controlled DOC in river water, reservoir water, and released water. DOC in the rivers tended to be affected by primary production. For reservoirs, the main controlling factors of DOC concentration varied by trophic state. For the mesotrophic Hongjiadu Reservoir, the effect of primary production on DOC concentration was obvious. For the eutrophic Dongfengdu Reservoir and the hypereutrophic Wujiangdu Reservoir, primary production was not significant and DOC came instead from soil and plant litter.     

Evolution of animal multicellularity stimulated by dissolved organic carbon in early Ediacaran ocean: DOXAM hypothesis

Oxygenation of the ocean is presumed to be an important factor stimulating the evolution of multicellular animals. The appearance of the Ediacaran‐type biota (ca 575 Ma) was assigned to the aftermath of the Gaskiers glaciation (ca 580 Ma), when substantial oceanic oxygenation is believed to have started. However, several lines of evidence reveal that at least sponges evolved before this oxygenation. For understanding the first stage of animal evolution, we propose the hypothesis that Dissolved Organic Carbon (DOC) Stimulated the evolution for Animal Multicellularity (DOXAM). Recent geochemical studies of the Ediacaran sedimentary sequences have indicated that a substantial DOC mass was developed in the stratified ocean after the Marinoan glaciation (655–635 Ma), and this was supported by the inorganic and organic carbon isotope profiles of the Doushantuo Formation in South China. The DOC mass was an oxygen consumer in the water column; however, it could have provided a food source for filter‐feeding animals such as sponges and cnidarians, and established a primitive food‐web. Such an ecological structure is recognized in modern deep‐sea coral mounds. Results from the integrated ocean drilling program (IODP) Expedition 307 for a mound in northeastern Atlantic suggested that organic carbon suspended around the density boundary in the water column is the key feature to feed the heterotrophic deep‐sea coral community. Our hypothesis is consistent with the fact that the two most primitive animal phyla (Porifera and Cnidaria) are filter feeders. The evolution of filter feeding ecosystems removed the DOC mass and may have contributed to ocean oxygenation in the terminal Neoproterozoic when animal evolution passed into the second stage, with the appearance of bilaterians.     

Total organic carbon fluxes of the Red River system (Vietnam)

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.     

Riverine inputs of total organic carbon and suspended particulate matter from the Pearl River Delta to the coastal ocean off South China

A total of 1008 samples were collected from the eight major riverine runoff outlets in the Pearl River Delta (PRD) during 2005-2006 to estimate the fluxes of total organic carbon (TOC) to the coastal ocean off South China. The average dissolved organic carbon (DOC) concentration was 1.67 mg/L with a range of 1.38-2.13 mg/L. Concentrations of particulate organic carbon (POC) ranged from 2.66-4.12% of total suspended particulate matter (SPM). The fluxes of TOC and SPM from the PRD via the eight outlets were 9.2 x 10(5) and 2.5 x 10(7)tons/yr, respectively. Temporal variations in POC and DOC were observed at all outlets due to the large variability in runoff levels because of the seasonality of rainfall, and the riverine discharge amount was an important factor controlling TOC flux. The net contribution of organic carbon from the PRD to the coastal ocean represented approximately 0.1-0.2% of total organic carbon transported by rivers worldwide.     

Release of dissolved organic carbon from upland peat

This study examines the release of dissolved organic carbon (DOC) from upland peat during the period of the autumn flushing. Hydroclimatic conditions were monitored in conjunction with measurements of absorbance and the E4/E6 ratio of the stream draining an 11·4 km² upland peat catchment in northern England. During two months of monitoring the effects of 67 separate rainfall events were examined showing that:

• The peat behaves hydrologically as if it were a two end‐member system consisting of old, interevent, and new, event, water. Runoff is initiated by percolation excess of new water at the acrotelm–catotelm interface.
• The discharge of dissolved organic matter behaves like a three end‐member system with the between‐event water being low in DOC and storm events being characterized by two types of water. Initial runoff being characterized by new water rich in DOC that gives way to new water depleted in DOC. This transition can be ascribed to the runoff progressing from throughflow within the acrotelm progressing to saturation‐excess overland flow.
• Depletion of DOC during storm events is accompanied by a change in the character of the DOC as the E4/E6 ratio changes. This suggests that the decrease in DOC during events is the result of exhaustion of reserves rather than changes in the flowpaths being utilized by runoff.
• The amount of carbon released in any event is critically dependent upon the time between events during which oxidation processes generate a reservoir of available carbon. Production of available carbon in the catchment is as high as 4·5 g C per day per m³ of peat, suggesting a turnover rate of peat of the order of 42 years. Copyright © 2002 John Wiley & Sons, Ltd.

     

The research of typical microbial functional group reveals a new oceanic carbon sequestration mechanism——A case of innovative method promoting scientific discovery

Marine microbes are major drivers of marine biogeochemical cycles and play critical roles in the ecosystems. Aerobic anoxygenic phototrophic bacteria(AAPB) are an important bacterial functional group with capability of harvesting light energy and wide distribution, and appear to have a particular role in the ocean's carbon cycling. Yet the global pattern of AAPB distribution was controversial at the beginning of the 21 st century due to the defects of the AAPB enumeration methods. An advanced time-series observation-based infrared epifluorescence microscopy(TIREM) approach was established to amend the existing AAPB quantitative deviation and led to the accurate enumeration of AAPB in marine environments. The abundance of AAPB and AAPB% were higher in coastal and continental shelf waters than in oceanic waters, which does not support the idea that AAPB are specifically adapted to oligotrophic conditions due to photosynthesis in AAPB acting a supplement to their organic carbon respiration. Further investigation revealed that dependence of AAPB on dissolved organic carbon produced by phytoplankton(PDOC) may limit their competition and control AAPB distribution. So, the selection of carbon sources by AAPB indicated that they can effectively fractionate the carbon flow in the sea. Enlightened by these findings, the following studies on the interactions between marine microbes and DOC led to the discovery of a new mechanism of marine carbon sequestration—the Microbial Carbon Pump(MCP). The conceptual framework of MCP addresses the sources and mechanism of the vast DOC reservoir in the ocean and represents a breakthrough in the theory of ocean carbon sequestration.     

Controls on fluvial carbon efflux from eroding peatland catchments

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.     

EXPORTS OF ORGANIC CARBON IN BRITISH RIVERS

This study provides the first detailed estimate of riverine organic carbon fluxes in British rivers, as well as highlighting major gaps in organic carbon data in national archives. Existing data on organic carbon and suspended solids concentrations collected between 1989 and 1993, during routine monitoring by the River Purification Boards (RPBs) in Scotland and the National River Authorities (NRAs) in England and Wales, were used with annual mean flows to estimate fluxes of dissolved and particulate organic carbon (DOC and POC) in British rivers. Riverine DOC exports during 1993 varied from 7·7–103·5 kg ha⁻¹ year⁻¹, with a median flux of 31·9 kg ha⁻¹ year⁻¹ in the 85 rivers for which data were available. There was a trend for DOC fluxes to increase from the south and east to the north and west. A predictive model based on mean soil carbon storage in 17 catchments, together with regional precipitation totals, explained 94% of the variation in the riverine DOC exports in 1993. This model was used to predict riverine DOC fluxes in regions where no organic carbon data were available. Calculated and predicted fluxes were combined to produce an estimate for exports of DOC to tidal waters in British rivers during 1993 of 0·68±0·07 Mt. Of this total, rivers in Scotland accounted for 53%, England 38% and Wales 9%. Scottish blanket peats would appear to be the largest single source of DOC exports in British rivers. An additional 0·20 Mt of organic carbon were estimated to have been exported in particulate form in 1993, approximately two–thirds of which was contributed by English rivers. It is suggested that riverine losses of organic carbon have the potential to affect the long-term dynamics of terrestrial organic carbon pools in Britain and that rivers may regulate increases in soil carbon pools brought about by climate change. © 1997 by John Wiley & Sons, Ltd.     

The Impact of Snail (Bellamya aeruginosa) Bioturbation on Sediment Characteristics and Organic Carbon Fluxes in an Eutrophic Pond

A mesocosm experiment was conducted for 32 days in an eutrophic pond to study the effects of the bioturbation of the freshwater snail, Bellamya aeruginosa, on the benthic environment and to further understand cycling of organic carbon in water containing algal blooms. Chlorophyll‐a (chl‐a), phaeopigment, and organic matter contents of sediment, sediment oxygen consumption (SOC), and dissolved organic carbon (DOC) fluxes were determined on day 1, 16, and 32, respectively. The SOC decreased on day 16 and increased on day 32 significantly with the increase in snail density. DOC fluxes showed a net sediment uptake in all enclosures throughout the experiment. DOC fluxes in the high and mid density treatments were lower than those of the control. The concentrations of chl‐a and phaeopigment in the sediment increased significantly with snail density, indicating that the presence of snails reduced the biomass of phytoplankton. The results suggest that freshwater snails, B. aeruginosa, could influence the algal biomass (chl‐a) of small water bodies by their bioturbation effects on sediment characteristics and the fluxes of organic carbon.     

The importance of sewage effluent discharge in the export of dissolved organic carbon from U.K. rivers

The flux of fluvial carbon from the terrestrial biosphere to the world's oceans is known to be an important component of the global carbon cycle, but within this pathway, the flux and return of carbon to the river network via sewage effluent has not been quantified. In this study, monitoring data from 2000 to 2016 for the dissolved organic carbon (DOC) concentration, biochemical oxygen demand, and chemical oxygen demand of the final effluent of sewage treatment works from across England were examined to assess the amount of DOC contributing to national‐scale fluvial fluxes of carbon. The study shows that the median concentration of DOC in final effluent was 9.4 compared with 4.8 mg C/L for all surface waters for the United Kingdom over the study period and that the DOC in final effluent significantly declined over the study period from 11.0 to 6.4 mg C/L. Rivers receiving sewage effluent showed a significant, on average 19%, increase in DOC concentration downstream of sewage discharges. At the scale of the United Kingdom, the flux of DOC in final effluent was 31 ktonnes C/year with a per capita export of 0.55 kg C/year and compared with an average annual flux of DOC from the United Kingdom of 859 ktonnes C/year, that is, only 3.6% of national‐scale flux. The lability of this DOC was limited, with only 7.4% loss of final effluent DOC concentration over in‐stream residence times of up to 5 days. The direct decline in DOC concentration from sewage treatment works was not large enough on its own to explain the declines observed in DOC concentration in U.K. rivers at their tidal limit.     

Dissolved oxygen as an indicator of bioavailable dissolved organic carbon in groundwater

Concentrations of dissolved oxygen (DO) plotted vs. dissolved organic carbon (DOC) in groundwater samples taken from a coastal plain aquifer of South Carolina (SC) showed a statistically significant hyperbolic relationship. In contrast, DO-DOC plots of groundwater samples taken from the eastern San Joaquin Valley of California (CA) showed a random scatter. It was hypothesized that differences in the bioavailability of naturally occurring DOC might contribute to these observations. This hypothesis was examined by comparing nine different biochemical indicators of DOC bioavailability in groundwater sampled from these two systems. Concentrations of DOC, total hydrolysable neutral sugars (THNS), total hydrolysable amino acids (THAA), mole% glycine of THAA, initial bacterial cell counts, bacterial growth rates, and carbon dioxide production/consumption were greater in SC samples relative to CA samples. In contrast, the mole% glucose of THNS and the aromaticity (SUVA(254)) of DOC was greater in CA samples. Each of these indicator parameters were observed to change with depth in the SC system in a manner consistent with active biodegradation. These results are uniformly consistent with the hypothesis that the bioavailability of DOC is greater in SC relative to CA groundwater samples. This, in turn, suggests that the presence/absence of a hyperbolic DO-DOC relationship may be a qualitative indicator of relative DOC bioavailability in groundwater systems.     

Sources of particulate and dissolved organic carbon in the St Lawrence River: isotopic approach

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.     

Organic carbon fluxes of a glacier surface: A case study of Foxfonna,a small Arctic glacier

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.     

Fluvial carbon flux from headwater peatland streams: significance of particulate carbon flux

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.