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1.
The biogeochemistry of methane in the sediments of Lake Caviahue was examined by geochemical analysis, microbial activity assays and isotopic analysis. The pH in the water column was 2.6 and increased up to a pH of 6 in the deeper sediment pore waters. The carbon isotope composition of CH4 was between − 65 and − 70‰ which is indicative for the biological origin of the methane. The enrichment factor ε increased from − 46‰ in the upper sediment column to more than − 80 in the deeper sediment section suggesting a transition from acetoclastic methanogenesis to CO2 reduction with depth. In the most acidic surface layer of the sediment (pH < 4) methanogenesis is inhibited as suggested by a linear CH4 concentration profile, activity assays and MPN analysis. The CH4 activity assays and the CH4 profile indicate that methanogenesis in the sediment of Lake Caviahue was active below 40 cm depth. At that depth the pH was above 4 and sulfate reduction was sulfate limited. Methane was diffusing with a flux of 0.9 mmol m− 2 d− 1 to the sediment surface where it was probably oxidized. Methanogenesis contributed little to the sediments carbon budget and had no significant impact on lake water quality. The high biomass content of the sediment, which was probably caused by the last eruption of Copahue Volcano, supported high rates of sulfate reduction which probably raised the pH and created favorable conditions for methanogens in deeper sediment layers.  相似文献   

2.
Authigenic carbonates were sampled in methane-enriched piston core sediments collected from gas venting sites on the western continental slope of the Ulleung Basin, East Sea of Korea. Multidisciplinary investigations on these carbonates, including the scanning electronic microscope (SEM) observations and mineralogical-geochemical compositions, were carried out to identify the carbon and oxygen sources and the forming mechanism of these carbonates. The authigenic carbonates from the study area correspond to semi-consolidated, compact concretions or nodules ranging from 2 to 9 cm in size. X-ray diffraction and electron microprobe analyses showed that most of the sampled carbonate concretions were composed of almost purely authigenic high-Mg calcite (10.7–14.3 mol% MgCO3). Characteristically, microbial structures such as filaments and rods, which were probably associated with the authigenic minerals, were abundantly observed within the carbonate matrix. The carbonates were strongly depleted in δ13C (−33.85‰ to −39.53‰ Peedee Belemnite (PDB)) and were enriched in δ18O (5.16–5.60‰ PDB), indicating that the primary source of carbon is mainly derived from the anaerobic oxidation of methane. Such methane probably originated from the destabilization of the underlying gas hydrates as strongly supporting from the enriched 18O levels. Furthermore, the strongly depleted δ13C values (−60.7‰ to −61.6‰ PDB) of the sediment void gases demonstrate that the majority of the gas venting at the Ulleung Basin is microbial methane by CO2 reduction. This study provides another example for the formation mechanism of methane-derived authigenic carbonates associated with gas-hydrate decomposition in gas-seeping pockmark environments.  相似文献   

3.
Tommeliten is a prominent methane seep area in the Central North Sea. Previous surveys revealed shallow gas-bearing sediments and methane gas ebullition into the water column. In this study, the in situ methane flux at Tommeliten is re-assessed and the potential methane transport to the atmosphere is discussed, with regards to the hydrographic setting and gas bubble modeling. We have compiled previous data, acquired new video and acoustic evidence of gas bubble release, and have measured the methane concentration, and its C-isotopic composition in the water column. Parametric subbottom sonar data reveal the three-dimensional extent of shallow gas and morphologic features relevant for gas migration. Five methane ebullition areas are identified and the main seepage area appears to be 21 times larger than previously estimated. Our video, hydroacoustic, subbottom, and chemical data suggest that ～1.5×106 mol CH4/yr (～26 tons CH4/yr) of methane gas is being released from the seepage area of Tommeliten. Methane concentration profiles in the vicinity of the gas seeps show values of up to 268 nM (～100 times background) close to the seafloor. A decrease in δ13C-CH4 values at 40 m water depth indicates an unknown additional biogenic methane source within the well oxygenated thermocline between 30 and 40 m water depth. Numerical modeling of the methane bubbles due to their migration and dissolution was performed to estimate the bubble-derived vertical methane transport, the fate of this methane in the water column, and finally the flux to the atmosphere. Modeling indicates that less than ～4% of the gas initially released at the seafloor is transported via bubbles into the mixed layer and, ultimately, to the atmosphere. However, because of the strong seasonality of mixing in the North Sea, this flux is expected to increase as mixing increases, and almost all of the methane released at the seafloor could be transferred into the atmosphere in the stormy fall and winter time.  相似文献   

4.
The concentrations and sea-to-air fluxes of dissolved methane (CH4) were investigated in the North Yellow Sea during August 2006, January, April and October 2007. Dissolved CH4 concentrations showed obvious seasonal variation, with maximum values occurring in summer and lowest values occurring in winter. The saturations of dissolved CH4 in surface waters ranged from 78.7% to 1679.7% with an average of 252.4%. The estimated atmospheric CH4 fluxes using the Liss and Merlivat (LM86), and Wanninkhof formulae (W92) were (4.2±4.7), (11.6±10.3), (8.5±12.7) and (0.2±1.0), and (6.9±7.3), (14.6±22.3), (13.8±14.3) and (0.4±1.7) μmol·(m2 d)−1, respectively, for spring, summer, autumn and winter. Based on the average annual atmospheric CH4 flux and the area of the North Yellow Sea, the annual CH4 emission was estimated to be (2.4×10−2–4.2×10−2) Tg a−1, which suggests that the North Yellow Sea was a net source of atmospheric CH4.  相似文献   

5.
Latent heat polynyas are regions generating strong ice formation, convection and extensive water mass formation. Here we report on the effects of these processes on resuspension of sediments and subsequent methane release from the seafloor and on the resulting excess methane concentration in surface water on a polar shelf during winter. The study is based on measurements of concentration and δ13C values of methane, water temperature, salinity, light transmission and sea ice data collected in March 2003 in Storfjorden, southern Svalbard. In winter, strong and persistent northeasterly winds create polynyas in eastern Storfjorden and cause ice formation. The resulting brine-enriched water cascades from the Storfjordbanken into the central depression thereby enhancing the turbulence near the seafloor. A distinct benthic nepheloid layer was observed reflecting the resuspension of sediments by the cascading dense bottom water. High concentrations of 13C-depleted methane suggest submarine discharge of methane with the resuspended sediments. As the source of the submarine methane, we propose recent bacterial methanogenesis near the sediment surface because of extremely high accumulation rates of organic carbon in Storfjorden. Convective mixing transports newly released methane from the bottom to the sea surface. This eventually results in an excess concentration in surface water with respect to the atmospheric equilibrium, and a sea-air flux of methane during periods of open water. When a new ice cover is formed, methane becomes trapped in the water column and subsequently oxidized. Thus, the residual methane is strongly enriched in 13C in relation to the δ13CCH4δ13CCH4 signature of atmospheric methane. Our results show that latent heat polynyas may induce a direct pathway for biogases like methane from sediments to the atmosphere through coupling of biogeochemical and oceanographic processes. Extrapolating these processes to all Arctic ocean polynyas, we estimate a transfer of CH4 between 0.005 and 0.02 Tg yr−1. This is not a large contribution but the fluxes from the polynyas are 20–200 times larger than the ocean average and the methane evasion process in polynyas is certainly one that can be altered under climate change.  相似文献   

6.
The build-up of methane in the hypolimnion of the eutrophic Lake Rotsee (Lucerne, Switzerland) was monitored over a full year. Sources and sinks of methane in the water column were characterized by measuring concentrations and carbon isotopic composition. In fall, high methane concentrations (up to 1 mM) were measured in the anoxic water layer. In the oxic layer, methane concentrations were much lower and the isotopic composition shifted towards heavy carbon isotopes. Methane oxidation rates peaked at the interface between oxic and anoxic water layers at around 8–10 m depth. The electron balance between the oxidants oxygen, sulphate, and nitrate, and the reductants methane, sulphide and ammonium, matched very well in the chemocline during the stratified season. The profile of carbon isotopic composition of methane showed strong indications for methane oxidation at the chemocline (including the oxycline). Aerobic methane oxidizing bacteria were detected at the interface using fluorescence in situ hybridization. Sequencing the responsible organisms from DGGE bands revealed that aerobic methanotrophs type I closely related to Methylomonas were present. Sulphate consumption occurred at the sediment surface and, only towards the end of the stagnation period, matched with a zone of methane consumption. In any case, the flux of sulphate below the chemocline was not sufficient to oxidize all the methane and other oxidants like nitrate, iron or manganese are necessary for the observed methane oxidation. Although most of the methane was oxidized either aerobically or anaerobically, Lake Rotsee was still a source of methane to the atmosphere with emission rates between 0.2 mg CH4 m?2 day?1 in February and 7 mg CH4 m?2 day?1 in November.  相似文献   

7.
Soil erosion has been identified as a potential global carbon sink since eroded organic matter is replaced at source and eroded material is readily buried. However, this argument has relied on poor estimates of the total fate of in‐transit particulates and could erroneously imply soil erosion could be encouraged to generate carbon stores. These previous estimates have not considered that organic matter can also be released to the atmosphere as a range of greenhouse gases, not only carbon dioxide (CO2), but also the more powerful greenhouse gases methane (CH4) and nitrous oxide (N2O). As soil carbon lost by erosion is only replaced by uptake of CO2, this could represent a considerable imbalance in greenhouse gas warming potential, even if it is not significant in terms of overall carbon flux. This work therefore considers the flux of particulate organic matter through UK rivers with respect to both carbon fluxes and greenhouse gas emissions. The results show that, although emissions to the atmosphere are dominated by CO2, there are also considerable fluxes of CH4 and N2O. The results suggest that soil erosion is a net source of greenhouse gases with median emission factors of 5.5, 4.4 and 0.3 tonnes CO2eq/yr for one tonne of fluvial carbon, gross carbon erosion and gross soil erosion, respectively. This study concludes that gross soil erosion would therefore only be a net sink of both carbon and greenhouse gases if all the following criteria are met: the gross soil erosion rate were very low (<91 tonnes/km2/yr); the eroded carbon were completely replaced by new soil organic matter; and if less than half of the gross erosion made it into the stream network. By establishing the emission factor for soil erosion, it becomes possible to properly account for the benefits of good soil management in minimizing losses of greenhouse gases to the atmosphere as a by‐product of soil erosion. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

8.
Sources and sinks of atmospheric methane   总被引：7，自引：0，他引：7  
In 1972 average mixing ratio of methane in the troposphere was 1.41 ppm and 1.3 ppmv for the northern and southern hemisphere, respectively, which corresponds to a total amount of 4×1015 g of CH4 present in the atmosphere. Most is of recent biologic origin.14C analyses show that no more than 20 percent is released by fossil sources. The various ecosystems producing CH4 are discussed and the total annual production is estimated to lie between 5.5×1014 g/yr and 11×1014 g/yr. The corresponding turnover times for atmospheric CH4 range from 4 to 7 yrs. The destruction of CH4 takes place mainly in the troposphere, most probably through the reaction of CH4 + OH CH3 + H2O. About 10 percent of the CH4 is destroyed in the stratosphere. The CH4 cycle contributes on the order of 1 percent to the atmospheric carbon cycle.  相似文献   

9.
Material fluxes associated with fluid expulsion at cold seeps and their contribution to oceanographic budgets have not been accurately constrained. Here we present evidence that the barium released at cold seeps along the San Clemente Fault zone may significantly impact the geochemical budget of barium within the basin. Barium fluxes at seep localities on the fault scarp, measured with benthic chambers, reach values as high as 5 mmol m−2 day−1. This is the largest dissolved barium flux measured to date at a cold seep. The discharge of barium-rich fluids results in formation of massive barite deposits along the escarpment wall. The deposits are young (approximately 8 yr) and appear to grow at a minimum rate of 0.2 cm yr−1. This rapid growth rate requires a barium efflux rate that is about two orders of magnitude higher than the measured dissolved flux. We believe that the discrepancy reflects a highly localized seepage system and that chambers positioned as close as possible to the growing chimneys did not sample the foci of fluid discharge. Transport of fine barite particles from the seeps may be responsible for excess rates of barium accumulation throughout the San Clemente Basin, relative to other basins in the California Margin. Based on a preliminary budget, we estimate that cold-seep barite is accumulating at the basin floor in San Clemente at a rate of 2 μmol m−2 day−1, a value that is comparable to the total barium accumulation rates driven by detrital and biogenic components in neighboring basins. Remobilization of cold-seep barite on the basin floor adds to that driven by the biogenic barium flux and results in benthic barium recycling rates (effluxes) within the San Clemente Basin that are as much as seven times higher than the effluxes from surrounding borderland basins. Our estimates imply that processes associated with fluid seepage along the San Clemente Fault significantly contribute to the basin’s barium cycle. The strontium isotopic composition of the seep barite is significantly different from marine ‘biogenic’ barite, which is known to accurately record seawater composition. In addition, the seep deposits are depleted in 226Ra relative to their modern biogenic counterparts, and are likely to be a source of radium-depleted particulate barium to the basin. Thus the impact of barite transport from seeps on the San Clemente escarpment to the basin floor might also have implications for the geochemistry of elements other than barium.  相似文献   

10.
In a dispersive coastal area under multiple organic enrichment sources, stable isotopes were used to trace organic sources of carbon and nitrogen in sediments and benthic macrofauna. The Bivalve Abra alba and the Polychaetes Nephtys sp. and Pectinaria (Lagis) koreni were reliable indicators of the input of terrestrial-derived organic matter into this coastal area, either originated in outfall sewage discharges or estuarine outflow. An isotopic depletion was observed up to 250 m from the outfall branches, much stronger in the biota than in the sediments. An enrichment of 2‰ in the sediments, and 2-6‰ in the species was noticed in sites located farther than 1500 m from the outfall. Depositivores and carnivores/omnivores gave the best picture of the extension of the sewage dispersion and incorporation into the food web.  相似文献   

11.
Twelve species of deep-sea fishes collected in 2005 from the western North Pacific, off-Tohoku, Japan were analyzed for organohalogen compounds. Among the compounds analyzed, concentrations of DDTs and PCBs (up to 23,000 and 12,400 ng/g lipid wt, respectively) were the highest. The present study is the foremost to report the occurrence of brominated flame retardants such as PBDEs and HBCDs in deep-sea organisms from the North Pacific region. Significant positive correlations found between δ15N (‰) and PCBs, DDTs and PBDEs suggest the high biomagnification potential of these contaminants in food web. The large variation in δ13C (‰) values observed between the species indicate multiple sources of carbon in the food web and specific accumulation of hydrophobic organohalogen compounds in benthic dwelling carnivore species like snubnosed eel. The results obtained in this study highlight the usefulness of deep-sea fishes as sentinel species to monitor the deep-sea environment.  相似文献   

12.
M. F. Billett  T. R. Moore 《水文研究》2008,22(12):2044-2054
Carbon dioxide (CO2) and methane (CH4) concentrations and evasion rates were measured in surface waters draining Mer Bleue peatland (Ontario, Canada) between spring and autumn 2005. All sites exhibit a consistent pattern of supersaturation throughout the year, which is broadly related to hydrological and temperature changes between spring snowmelt and autumn freezing. Both measurements and estimates of CO2 and CH4 evasion from open water to the atmosphere suggest that parts of the catchment (including beaver dams) are significant degassing hot spots. We present data showing how vertical gaseous carbon fluxes compare with lateral carbon fluxes and make an initial estimate of the importance to the overall carbon budget of CO2 and CH4 evasion to the atmosphere from water surfaces at Mer Bleue. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

13.
An 8-m continuous sediment core, approximately 250-ky-old at the bottom, from Academician Ridge in Lake Baikal, has been analyzed for the stable isotopes of carbon, nitrogen and sulfur, in order to study the paleoclimatic and paleobiological changes that occurred in the Eurasian continental interior. These isotopic changes are closely related to changes in vertical lake-water circulation between glacial and interglacial periods. Sedimentary organic carbon in cool periods is more enriched in 13C (−23.8‰ on average) than that in warm periods (−27.0‰ on average). The 13C-enrichment of organic carbon suggests a decrease of land-derived organic matter influx to the lake, less precipitation, and loss of terrestrial vegetation around Lake Baikal in cool periods. Pyrite in high total sulfur/total organic carbon (TS/TOC) layers shows strong depletion in 34S (−20.8‰ to −32.4‰) during climate transitions from glacial to interglacial periods at the beginning of oxygen isotope stages (OIS) 1, 5 and 7. The 34S-depleted pyrite indicates augmentation of dissimilatory sulfate reduction by sulfate reducing bacteria (SRB) at the sediment-water interface. Enhancement of aqueous sulfate concentrations and limitation of oxygen circulation to the surface sediments might also occur in the climate transition periods. The δ15N values of total nitrogen increase abruptly by ∼2‰ just after the δ34S negative peaks, which may result from low nutrient concentrations in the euphotic zone associated with water circulation changes in Lake Baikal.  相似文献   

14.
We provide two new determinations of the oxygen isotopic composition of seawater during the last glacial maximum (LGM). High-resolution oxygen isotopic measurements were made on interstitial waters from Ocean Drilling Program (ODP) Sites 1168 and 1170 in the southeast Indian Ocean sector of the Southern Ocean. We use a diffusion-advection numerical model to calculate the glacial-interglacial change in bottom-water δ18Osw from the pore water δ18O profiles; the first such determinations from this part of the oceans. Statistical analyses of the model runs indicate that Circumpolar Deep Water (CDW) δ18Osw changed by 1.0-1.1±0.15‰ since the last glacial maximum (LGM). Our results are consistent with a previous calculation from a South Atlantic Southern Ocean location (ODP Site 1093) also situated within CDW. The new values determined in this study, together with previous estimates, are converging on a global average Δδ18Osw of 1.0-1.1‰.Using the calculated bottom-water δ18Osw, we have extracted the temperature component from the benthic foraminiferal δ18O record at Sites 1168 and 1170. Since the LGM, bottom waters at these two sites warmed by 2.6 and 1.9°C, respectively. The absolute temperature estimates for the LGM (−0.5°C [Θ=−0.6°C] at Site 1168 and −0.2°C [Θ=−0.4°C] at Site 1170) are slightly warmer than those reported from previous studies using the same technique, but are consistent with more homogenous deep-ocean temperatures during the LGM relative to the modern.  相似文献   

15.
A holistic ecosystem simulation model has been developed for the Cumberland Basin and upper Chignecto Bay, a turbid macrotidal estuary at the head of the Bay of Fundy. This one-dimensional deterministic model has three compartments, three boundaries and three interacting submodels (physical, pelagic and benthic). Twenty-eight biological state variables represent broad functional groups of organisms and non-living organic carbon pools. All major components of the estuarine ecosystem are included. At the present stage of development, individual pelagic state variables give reasonable annual simulations which are in general agreement with available calibration data. Major problems remain with some benthic state variables, especially the subtidal ones about which little is known. In aggregate, the model performs well and output at the ecosystem level agrees with field observations. In the Cumberland Basin water column, annual community respiration exceeds phytoplankton net production (1–3 g C m−3) by a factor of 2–5 suggesting the importance of carbon imported from surrounding saltmarshes and the seaward boundary. Annual community respiration and microalgal net production (28 g C m−2) on the other hand are closely balanced in intertidal sediments. Respiration in subtidal sediments is entirely dependent upon sedimented carbon. The model supports the hypothesis that the Cumberland Basin is a heterotrophic ecosystem with low primary production which requires imported organic carbon to support the production and respiration of higher trophic levels.  相似文献   

16.
To clarify the sources and transformation of NO3− on the Pacific coast of Japan, observations over the continental shelf were conducted during the summer in 2005 and 2006 when the Kuroshio flowed close to and away from the coastal area, respectively. Below the halocline, there are two prominent salinity peaks that originated in two different waters. In the subsurface layer, the salinity maximum (Smax) was indicative of the Kuroshio Water (KW), while the salinity minimum (Smin) in the middle layer at ∼400 m depth was indicative of the North Pacific Intermediate Water (NPIW). δ15NNO3 ranged from 4.1‰ to 5.1‰ with a mean of 4.8±0.4‰ in the deeper water around Smin. Below 50 m depth over the shelf break, δ15NNO3 values (3.1±0.8‰ in 2005 and 4.6±0.3‰ in 2006) clearly increased as contribution of NPIW increased in 2006. On the contrary, subsurface δ15N of NO3− values (−1.1±0.1‰) remained unchanged in both years, although the contribution of the KW to the subsurface water changed significantly. This suggests that the source of NO3− has little effect on the δ15N of NO3− in this layer. The negative δ15N values also coincided with the base of the chlorophyll maximum layer suggesting that these isotopic signals must be evidence of active nitrification in the upper layer.  相似文献   

17.
内陆水体好氧甲烷氧化过程研究进展   总被引：1，自引：0，他引：1  
秦宇  黄璜  李哲  鲁伦慧  汤琼  苏友恒  李欣芮 《湖泊科学》2021,33(4):1004-1017
内陆水体是全球碳循环的关键组成部分,是大气中甲烷(CH_4)的重要来源,每年从内陆淡水与自然湿地排放进入大气的CH4约为185～357 Tg/a.通常,内陆水体中CH_4主要由分布于水层底部的厌氧区或沉积层内的产甲烷菌介导产生,其向水层表面传输的过程中易被甲烷氧化菌所氧化.甲烷氧化菌可分为好氧甲烷氧化菌和厌氧甲烷氧化菌,有氧条件下,由好氧甲烷氧化菌介导的好氧甲烷氧化过程是水体中甲烷氧化过程的主要形式,湖泊底部产生的CH_4总量中约有99%可以被上覆水体中的好氧甲烷氧化过程所消耗.本文收集文献综合分析阐明,好氧甲烷氧化过程是由水环境因子、水文条件以及不同内陆水体的生态系统特征共同调控,同时也表现在了好氧甲烷氧化菌的生境偏好上.复杂的调控过程构建了内陆水体向大气输送CH_4的动态平衡,并最终反映在内陆水体对全球CH_4循环、碳循环作出的贡献上.  相似文献   

18.
Our understanding of the ancient ocean-atmosphere system has focused on oceanic proxies. However, the study of terrestrial proxies is equally necessary to constrain our understanding of ancient climates and linkages between the terrestrial and oceanic carbon reservoirs. We have analyzed carbon-isotope ratios from fossil plant material through the Valanginian and Lower Hauterivian from a shallow-marine, ammonite-constrained succession in the Crimean Peninsula of the southern Ukraine in order to determine if the Upper Valanginian positive carbon-isotope excursion is expressed in the atmosphere. δ13Cplant values fluctuate around − 23‰ to − 22‰ for the Valanginian-Hauterivian, except during the Upper Valanginian where δ13Cplant values record a positive excursion to ∼− 18‰. Based upon ammonite biostratigraphy from Crimea, and in conjunction with a composite Tethyan marine δ13Ccarb curve, several conclusions can be drawn: (1) the δ13Cplant record indicates that the atmospheric carbon reservoir was affected; (2) the defined ammonite correlations between Europe and Crimea are synchronous; and (3) a change in photosynthetic carbon-isotope fractionation, caused by a decrease in atmospheric pCO2, occurred during the Upper Valanginian positive δ13C excursion. Our new data, combined with other paleoenvironmental and paleoclimatic information, indicate that the Upper Valanginian was a cool period (icehouse) and highlights that the Cretaceous period was interrupted by periods of cooling and was not an equable climate as previously thought.  相似文献   

19.
Peatlands are among the largest long‐term soil carbon stores, but their degradation can lead to significant carbon losses. This study considers the carbon budget of peat‐covered sites after restoration, following degradation by past wildfires. The study measured the carbon budget of eight sites: four restored‐revegetated sites, two unrestored bare soil control sites, and two intact vegetated controls over two years (2006–2008). The study considered the following flux pathways: dissolved organic carbon (DOC); particulate organic carbon (POC); dissolved carbon dioxide (CO2); primary productivity; net ecosystem respiration, and methane (CH4). The study shows that unrestored, bare peat sites can have significant carbon losses as high as 522 ± 3 tonnes C/km2/yr. Most sites showed improved carbon budgets (decreased source and/or increased sink of carbon) after restoration; this improvement was mainly in the form of a reduction in the size of the net carbon source, but for one restored site the measured carbon budget after four years of restoration was greater than observed for vegetated controls. The carbon sequestration benefit of peatland restoration would range between 122 and 833 tonnes C/km2/yr. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

20.
Estimates of greenhouse gas evasion from rivers have been refined over the past decades to constrain their role in global carbon cycle processes. However, despite 55% of the human population living in urban areas, urban rivers have had limited attention. We monitored carbon dynamics in an urbanized river (River Kelvin, 331 km2, UK) to explore the drivers of dissolved carbon lateral and vertical export. Over a 2-year sampling period, riverine methane (CH4) and carbon dioxide (CO2) concentrations were consistently oversaturated with respect to atmospheric equilibria, leading to continual degassing to the atmosphere. Carbon stable isotopic compositions (δ13C) indicated that terrestrially derived carbon comprised most of the riverine CH4 and dissolved CO2 (CO2*) load while dissolved inorganic carbon (DIC) from groundwater was the main form of riverine DIC. The dynamics of CH4, CO2*, and DIC in the river were primarily hydrology-controlled, that is, [CH4] and [CO2*] both increased with elevated discharge, total [DIC] decreased with elevated discharge while the proportion of biologically derived DIC increased with increasing discharge. The concentration of dissolved organic carbon (DOC) showed a weak relationship with river hydrology in summer and autumn and was likely influenced by the combined sewer overflows. Carbon emission to the atmosphere is estimated to be 3.10 ± 0.61 kg C·m−2·yr−1 normalized to water surface area, with more than 99% emitted as CO2. Annual carbon loss to the coastal estuary is approximately 4.69 ± 0.70 Gg C yr−1, with annual DIC export approximately double that of DOC. Per unit area, the River Kelvin was a smaller carbon source to the atmosphere than natural rivers/streams but shows elevated fluxes of DIC and DOC under comparable conditions. This research illustrates the role urban systems may have on riverine carbon dynamics and demonstrates the potential tight link between urbanization and riverine carbon export.  相似文献   

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