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1.
Surface waters associated with peatlands, supersaturated with CO2 and CH4 with respect to the atmosphere, act as important pathways linking a large and potentially unstable global repository of C to the atmosphere. Understanding the drivers and mechanisms which control C release from peatland systems to the atmosphere will contribute to better management and modelling of terrestrial C pools. We used non‐dispersive infra‐red (NDIR) CO2 sensors to continuously measure gas concentrations in a beaver pond at Mer Bleue peatland (Canada); measurements were made between July and August 2007. Concentrations of CO2 in the surface water (10 cm) reached 13 mg C l?1 (epCO2 72), and 26 mg C l?1 (epCO2 133) at depth (60 cm). The study also showed large diurnal fluctuations in dissolved CO2 which ranged in amplitude from ～1·6 mg C l?1 at 10 cm to ～0·2 mg C l?1 at 60 cm depth. CH4 concentration and supersaturation (epCH4) measured using headspace analysis averaged 1·47 mg C l?1 and 3252, respectively; diurnal cycling was also evident in CH4 concentrations. Mean estimated evasion rates of CO2 and CH4 over the summer period were 44·92 ± 7·86 and 0·44 ± 0·25 µg C m?2s?1, respectively. Open water at Mer Bleue is a significant summer hotspot for greenhouse gas emissions within the catchment. Our results suggest that CO2 concentrations during the summer in beaver ponds at Mer Bleue are strongly influenced by biological processes within the water column involving aquatic plants and algae (in situ photosynthesis and respiration). In terms of carbon cycling, soil‐stream connectivity at this time of year is therefore relatively weak. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

2.
Methane emissions from hydroelectric reservoirs can comprise a considerable portion of anthropogenic methane. However, lack of data on CH4 emissions in different geographical regions and high spatial‐temporal variability in the emission rates of reservoirs has led to uncertainties regarding regional emission estimates of CH4. In the subtropical plateau climate region, we used the Ertan hydroelectric reservoir as a study area. The CH4 flux at the air‐water interface was assessed by floating chambers and factors influencing emissions, including the distance from the dam, water depth, seasonal variation in wet and dry season, air‐water temperature gradient and wind speed, and was also studied through a year‐long systematic sampling and monitoring experiment. The results showed that the surface of the reservoir was a source of CH4 during the sampling period and the annual average CH4 flux was 2·80 ± 1·52 mg m?2 d?1. CH4 flux (and its variation) was higher in the shallow water areas than in the deep‐water areas. CH4 flux near the dam was significantly higher than that of other locations farther from the dam in the dry season. The seasonal variations of CH4 emission in wet and dry seasons were minor and significant diurnal variations were observed in wet and dry seasons. Exponential relationships between the CH4 flux and air‐water temperature gradient were found. Air‐water temperature gradient was an important factor influencing diurnal variations of CH4 flux in the Ertan hydroelectric reservoir. These results indicate that systematic sampling is needed to better estimate CH4 flux through coverage of the spatial variation of different water depths, measuring‐point distance from the dam, seasonal variation in wet and dry seasons and changes in climate factors (such as air‐water temperature gradient). Our results also provide a fundamental parameter for CH4 emission estimation of global reservoirs. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

3.
以三峡水库香溪河库湾为研究对象,采用原位加密采样(2021年5月)和室内培养方法,结合沉积物特性与水环境因子分析,探讨了香溪河库湾沉积物甲烷(CH4)释放潜力、沉积物-水界面CH4产生和氧化通量空间分布规律及其影响因素。结果表明:三峡水库泄水期间,香溪河库湾沉积物CH4释放潜力的变化范围是6.35-2029.37 mg/(kg·d),沉积物-水界面CH4产生通量和氧化通量的变化范围分别为0.04～0.73、0.03～0.62 mmol/(m2·d);空间上,沉积物CH4释放潜力、沉积物-水界面CH4产生及氧化通量在香溪河库湾和各典型横切面(XX02、XX05和XX06)间表现出空间差异性,主要受水深、TOC和温度的影响。垂向上,CH4产生速率随沉积物深度的增加而减小,表层20 cm沉积物CH4释放潜力占整柱沉积物的70%,可以用于估算库湾沉积物CH4释放潜力。此外,沉积...  相似文献   

4.
The influence of winter on methane (CH4) stored in pore water and emitted through snow was investigated in a temperate poor fen in New Hampshire over two winters. Methane accumulated beneath ice layers (1 cm) deposited by freezing rain, resulting in snow-pore air mixing ratios as high as 140 ppmv during the first winter and 600 ppmv during the second. An early winter snow crust of 300 kg m?3 caused no discontinuity in a linear mixing ratio profile and therefore was not observed to retard snowpack emissions. Methane concentration-depth profiles in pore water steepened and concentrations increased by as much as 400 μM at the 10 and 20 cm depths as the ice cover formed. This suggests that the peat-ice cover plays an important part in CH4 build-up in pore water by limiting the transport of gases between the peat and the atmosphere. Pore water concentrations gradually declined through late winter. The seasonality of dissolved CH4 in pore water over two winters and one summer showed an average annual amplitude of 1.3 gCH4m?2 (25–75cm depth range), with a winter maximum of 4.7gCH4m?2. Emissions during the winter with average snowfall accounted for a larger percentage (9.2% in 1993–1994) of total annual emission than the winter with below-average snowfall and warmer air temperature (2% in 1994–1995). Emissions averaged 56 and 26mg m?2 day?1 during the first and second winter (December, January and February), respectively.  相似文献   

5.
Entrapped gas bubbles in peat can alter the buoyancy, storativity, void ratio and expansion/contraction properties of the peat. Moreover, when gas bubbles block water‐conducting pores they can significantly reduce saturated hydraulic conductivity and create zones of over‐pressuring, perhaps leading to an alteration in the magnitude and direction of groundwater flow and solute transport. Some previous researches have demonstrated that these zones of over‐pressuring are not observed by the measurements of pore‐water pressures using open‐pipe piezometers in peat; rather, they are only observed with pressure transducers sealed in the peat. In has been hypothesized that open‐pipe piezometers vent entrapped CH4 to the atmosphere and thereby do not permit the natural development of zones of entrapped gas. Here we present findings of the study to investigate whether piezometers vent subsurface CH4 to the atmosphere and whether the presence of piezometers alters the subsurface concentration of dissolved CH4. We measured the flux of methane venting from the piezometers and also determined changes in pore‐water CH4 concentration at a rich fen in southern Ontario and a poor fen in southern Quebec, in the summer of 2004. Seasonally averaged CH4 flux from piezometers was 1450 and 37·8‐mg CH4 m?2 d?1 at the southern Ontario site and Quebec site, respectively. The flux at the Ontario site was two orders of magnitude greater than the diffusive flux at the site. CH4 pore‐water concentrations were significantly lower in open piezometers than in water taken from sealed samplers at both the Ontario and Quebec sites. The flux of CH4 from piezometers decreased throughout the season suggesting that CH4 venting through the piezometer exceeded the rate of methanogenesis in the peat. Consequently we conclude that piezometers may alter the gas dynamics of some peatlands. We suggest that less‐invasive techniques (e.g. buried pressure transducers, tracer experiments) are needed for the accurate measurement of pore‐water pressures and hydraulic conductivity in peatlands with a large entrapped gas component. Furthermore, we argue that caution must be made in interpreting results from previous peatland hydrology studies that use these traditional methods. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

6.
Methane fermentation is widely used to dispose of sewage sludge at wastewater treatment plants (WWTPs), due to production of renewable energy in the form of biogas. Antibiotics present in wastewater may accumulate in a sewage sludge. The aim of the present study is to investigate the impact of three antibiotics from different classes in three different doses on methane production from sewage sludge. For this purpose, metronidazole (MET), amoxicillin (AMO), and ciprofloxacin (CIP) are individually added to anaerobic reactors with sewage sludge collected from municipal WWTP. The antibiotics’ highest concentration (1024 mg kg?1 of AMO; 512 mg kg?1 of MET and CIP) lowers methane production and methane content in biogas. MET exerts the most marked effect and lowers methane production to 36.8 ± 3.7 mL CH4 kg?1 volatile solids. Tested antibiotics probably inhibit methanogenic archaea, which results in volatile fatty acids (VFAs) accumulation. Addition of MET results in accumulation of many kinds of VFAs with the highest concentration of acetic acid (17.52 ± 1.85 g L?1). The addition of of AMO results in accumulation of butyric acid only (253.00 ± 15.89 g L?1). However, addition of CIP results in accumulation of mainly acetic acid (7.58 ± 0.82 g L?1) and isovaleric acid (2.01 ± 0.41 g L?1). Next, synergistic effect of these antibiotics in a low concentration of 16 mg kg?1 of AMO, 8 mg kg?1 of MET, and 2 mg kg?1 of CIP is measured in semi‐continuous conditions and causes inbibition of methane production and accumulation of VFAs.  相似文献   

7.
Prealpine Lake Lungern shows in spite of low primary production rates (120 g C/m2. year) and full winter overturns a complete oxygen depletion in the deepest hypolimnion (65–70 m below surface) towards the end of summer stagnation. Periodical examinations of O2- and CH4-concentrations, CH4-oxidation rates and temperature in the water column during 1975/76 enabled an O2-balance of Lake Lungern. The direct measurement of the CH4-flux at the sediment-water-interface and of the CH4-concentrations in sediment cores as well as the determination of the age of methane bubbles lead to the conclusion, that the hypolimnic oxygen depletion is partly due to the oxidation of fossile methane penetrating the lake from below.   相似文献   

8.
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   

9.
This study examines the effect of drawdown on the timing and magnitude of suspended solids and associated phosphorus export from a 12 ha reservoir located in an urbanized watershed in southern Ontario, Canada. Water level in Columbia Lake was lowered by 1·15 m over a 2‐week period in November 2001. The total phosphorus (TP) concentrations ranged from 63 to 486 µg L?1 in Columbia Lake and 71 to 373 µg L?1 at its outflow. All samples exceeded the Provincial Water Quality Objective of 30 µg TP L?1. Outflow concentrations of suspended solids and TP increased significantly with decreasing lake level and were attributed to the resuspension of cohesive bottom sediments that occurred at a critical threshold lake level (0·65 m below summer level). Suspended solids at the outflow consisted of flocculated cohesive materials with a median diameter (D50) of c. 5 µm. Particulate organic carbon accounted for 8·5% of the suspended solids export by mass. A total mass of 18·5 t of suspended solids and 62·6 kg TP was exported from Columbia Lake, which represents a significant pulse of sediment‐associated P to downstream environments each autumn during drawdown. The downstream impacts of this release can be minimized if the water level in Columbia Lake is lowered no more than 0·5 m below summer levels. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

10.
In general, the rate and timing of calcite precipitation is in part affected by variations in cave air CO2 concentrations. Knowledge of cave ventilation processes is required to quantify the effect variations in CO2 concentrations have on speleothem deposition rates and thus paleoclimate records. In this study we use radon-222 (222Rn) as a proxy of ventilation to estimate CO2 outgassing from the cave to the atmosphere, which can be used to infer relative speleothem deposition rates. Hollow Ridge Cave, a wild cave preserve in Marianna, Florida, is instrumented inside and out with multiple micro-meteorological sensor stations that record continuous physical and air chemistry time-series data. Our time series datasets indicate diurnal and seasonal variations in cave air 222Rn and CO2 concentrations, punctuated by events that provide clues to ventilation and drip water degassing mechanisms. Average cave air 222Rn and CO2 concentrations vary seasonally between winter (222Rn = 50 dpm L? 1, where 1 dpm L? 1 = 60 Bq m? 3; CO2 = 360 ppmv) and summer (222Rn = 1400 dpm L? 1; CO2 = 3900 ppmv). Large amplitude diurnal variations are observed during late summer and autumn (222Rn = 6 to 581 dpm L? 1; CO2 = 360 to 2500 ppmv).We employ a simple first-order 222Rn mass balance model to estimate cave air exchange rates with the outside atmosphere. Ventilation occurs via density driven flow and by winds across the entrances which create a ‘venturi’ effect. The most rapid ventilation occurs 25 m inside the cave near the entrance: 45 h? 1 (1.33 min turnover time). Farther inside (175 m) exchange is slower and maximum ventilation rates are 3 h? 1 (22 min turnover time). We estimate net CO2 flux from the epikarst to the cave atmosphere using a CO2 mass balance model tuned with the 222Rn model. Net CO2 flux from the epikarst is highest in summer (72 mmol m? 2 day? 1) and lowest in late autumn and winter (12 mmol m? 2 day? 1). Modeled ventilation and net CO2 fluxes are used to estimate net CO2 outgassing from the cave to the atmosphere. Average net CO2 outgassing is positive (net loss from the cave) and is highest in late summer and early autumn (about 4 mol h? 1) and lowest in winter (about 0.5 mol h? 1). Modeling of ventilation, net CO2 flux from the epikarst, and CO2 outgassing to the atmosphere from cave monitoring time-series can help better constrain paleoclimatic interpretations of speleothem geochemical records.  相似文献   

11.
Soil denitrification in reservoir shoreline wetlands is an important process for removing excess inorganic nitrogen from upland runoff and controlling eutrophication in aquatic ecosystems. As yet, little is known about the influence of vegetation characteristics on the soil denitrification potential in reservoir shoreline wetlands, although vegetation can affect both denitrifying bacteria and soil properties. In this study, we measured the spatial variability of denitrification enzyme activity (DEA) using acetylene block method in shoreline wetlands of the Danjiangkou Reservoir, a water source of the South‐to‐North Water Transfer Project in China. Results indicated that DEA ranged from 0.001 to 2.449 µg N (N2O) g?1 h?1, with a mean of 0.384 µg N (N2O) g?1 h?1. DEA varied significantly among five representative plant communities and the highest DEA (0.248–2.449 µg N (N2O) g?1 h?1) was observed in the Polygonum hydropiper community. Plant biomass and vegetation cover were significantly and positively related to DEA and together explained 44.2% of the total variance. These results suggest that vegetation characteristics should also be considered in assessing soil denitrification capacity and restoring shoreline wetlands for nitrogen pollution removal in the Danjiangkou Reservoir after dam heightening.  相似文献   

12.
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   

13.
Wetlands often form the transition zone between upland soils and watershed streams, however, stream–wetland interactions and hydrobiogeochemical processes are poorly understood. We measured changes in stream nitrogen (N) through one riparian wetland and one beaver meadow in the Archer Creek watershed in the Adirondack Mountains of New York State, USA from 1 March to 31 July 1996. In the riparian wetland we also measured changes in groundwater N. Groundwater N changed significantly from tension lysimeters at the edge of the peatland to piezometer nests within the peatland. Mean N concentrations at the peatland perimeter were 1·5, 0·5 and 18·6 µmol L?1 for NH4+, NO3? and DON (dissolved organic nitrogen), respectively, whereas peatland groundwater N concentration was 56·9, 1·5 and 31·6 µmol L?1 for NH4+, NO3? and DON, respectively. The mean concentrations of stream water N species at the inlet to the wetlands were 1·5, 10·1 and 16·9 µmol L?1 for NH4+, NO3? and DON, respectively and 1·6, 28·1 and 8·4 µmol L?1 at the wetland outlet. Although groundwater total dissolved N (TDN) concentrations changed more than stream water TDN through the wetlands, hydrological cross‐sections for the peatland showed that wetland groundwater contributed minimally to stream flow during the study period. Therefore, surface water N chemistry was affected more by in‐stream N transformations than by groundwater N transformations because the in‐stream changes, although small, affected a much greater volume of water. Stream water N input–output budgets indicated that the riparian peatland retained 0·16 mol N ha?1 day?1 of total dissolved N and the beaver meadow retained 0·26 mol N ha?1 day?1 during the study period. Nitrate dominated surface water TDN flux from the wetlands during the spring whereas DON dominated during the summer. This study demonstrates that although groundwater N changed significantly in the riparian peatland, those changes were not reflected in the stream. Consequently, although in‐stream changes of N concentrations were less marked than those in groundwater, they had a greater effect on stream water chemistry—because wetland groundwater contributed minimally to stream flow. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

14.
This study combined water- and sediment flux measurements with mass balances of dissolved gas and inorganic matter to determine the importance of pelagic and benthic processes for whole-system metabolism in a eutrophic fluvial lake. Mass balances of dissolved O2, inorganic carbon (DIC), nitrogen (DIN), phosphorous (SRP), particulate N (PN) and P (PP) and Chl a were calculated at a nearly monthly frequency by means of repeated sampling at the lake inlet and outlet. Simultaneously, benthic fluxes of gas and nutrients, including denitrification rates, and the biomass of the dominant pleustophyte (Trapa natans) were measured, and fluxes of O2 and CO2 across the water–atmosphere interface were estimated from diel changes in outlet concentrations. On an annual scale, Middle Lake exhibited CO2 supersaturation, averaging 313% (range 86–562%), but was autotrophic with a net O2 production (6.35 ± 2.05 mol m−2 y−1), DIC consumption (−31.18 ± 18.77 mol m−2 y−1) and net export of Chl a downstream (8.38 ± 0.95 mol C m−2 y−1). Phytoplankton was the main driver of Middle Lake metabolism, with a net primary production estimated at 33.24 mol O2 m−2 y−1, corresponding to a sequestration of 4.18 and 0.26 mol m−2 y−1 of N and P, respectively. At peak biomass, T. natans covered about 18% of Middle Lake’s surface and fixed 2.46, 0.17 and 0.02 mol m−2 of C, N and P, respectively. Surficial sediments were a sink for O2 (−14.47 ± 0.65 mol O2 m−2 y−1) and a source of DIC and NH4 + (18.84 ± 2.80 mol DIC m−2 y−1 and 0.83 ± 0.16 mol NH4 + m−2 y−1), and dissipated nitrate via denitrification (1.44 ± 0.11 mol NO3 − m−2 y−1). Overall, nutrient uptake by primary producers and regeneration from sediments were a minor fraction of external loads. This work suggests that the creation of fluvial lakes can produce net autotrophic systems, with elevated rates of phytoplanktonic primary production, largely sustained by allochtonous nutrient inputs. These hypereutrophic aquatic bodies are net C sinks, although they simultaneously release CO2 to the atmosphere.  相似文献   

15.
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   

16.
A critical factor controlling changes in the acidity of coastal waters is the alkalinity of the water. Concentrations of alkalinity are determined by supply from rivers and by in situ processes such as biological production and denitrification. A 2-year study based on 15 cruises in Liverpool Bay followed the seasonal cycles of changing concentrations of total alkalinity (TA) and total dissolved inorganic carbon (DIC) in relation to changes caused by the annual cycle of biological production during the mixing of river water into the Bay. Consistent annual cycles in concentrations of nutrients, TA and DIC were observed in both years. At a salinity of 31.5, the locus of primary production during the spring bloom, concentrations of NO x decreased by 25 ± 4 μmol kg−1 and DIC by 106 ± 16 μmol kg−1. Observed changes in TA were consistent with the uptake of protons during primary biological production. Concentrations of TA increased by 33 ± 8 μmol kg−1 (2009) and 33 ± 15 μmol kg−1 (2010). The impact of changes in organic matter on the measured TA appears likely to be small in this area. Thomas et al. (2009) suggested that denitrification may enhance the CO2 uptake of the North Sea by 25%, in contrast we find that although denitrification is a significant process in itself, it does not increase concentrations of TA relative to those of DIC and so does not increase buffer capacity and potential uptake of CO2 into shelf seawaters. For Liverpool Bay historical data suggest that higher concentrations of TA during periods of low flow are likely to contribute in part to the observed change in TA between winter and summer but the appropriate pattern cannot be identified in recent low-frequency river data. On a wider scale, data for the rivers Mersey, Rhine, Elbe and Weser show that patterns of seasonal change in concentrations of TA in river inputs differ between river systems.  相似文献   

17.
Cave air PCO2 at two Irish sites varied dramatically on daily to seasonal timescales, potentially affecting the timing of calcite deposition and consequently climate proxy records derived from stalagmites collected at the same sites. Temperature-dependent biochemical processes in the soil control CO2 production, resulting in high summer PCO2 values and low winter values at both sites. Large Large-amplitude, high-frequency variations superimposed on this seasonal cycle reflect cave air circulation. Here we model stalagmite growth rates, which are controlled partly by CO2 degassing rates from drip water, by considering both the seasonal and high-frequency cave air PCO2 variations. Modeled hourly growth rates for stalagmite CC-Bil from Crag Cave in SW Ireland reach maxima in late December (0.063 μm h− 1) and minima in late June/early July (0.033 μm h− 1). For well-mixed ‘diffuse flow’ cave drips such as those that feed CC-Bil, high summer cave air PCO2 depresses summer calcite deposition, while low winter PCO2 promotes degassing and enhances deposition rates. In stalagmites fed by well-mixed drips lacking seasonal variations in δ18O, integrated annual stalagmite calcite δ18O is unaffected; however, seasonality in cave air PCO2 may influence non-conservative geochemical climate proxies (e.g., δ13C, Sr/Ca). Stalagmites fed by ‘seasonal’ drips whose hydrochemical properties vary in response to seasonality may have higher growth rates in summer because soil air PCO2 may increase relative to cave air PCO2 due to higher soil temperatures. This in turn may bias stalagmite calcite δ18O records towards isotopically heavier summer drip water δ18O values, resulting in elevated calcite δ18O values compared to the ‘equilibrium’ values predicted by calcite–water isotope fractionation equations. Interpretations of stalagmite-based paleoclimate proxies should therefore consider the consequences of cave air PCO2 variability and the resulting intra-annual variability in calcite deposition rates.  相似文献   

18.
Hydroelectric power is an important energy source to meet the growing demand for energy, and large amounts of water are consumed to generate this energy. Previous studies often assumed that the water footprint of hydroelectric power equaled the reservoir’s water footprint, but failed to allocate the reservoir water footprint among the many beneficiaries; dealing with this allocation remains a challenge. In this study, we developed a new approach to quantify the water footprint of hydroelectric power (WFh) by separating it from the reservoir water footprint (WF) using an allocation coefficient (ηh) based on the ratio of the benefits from hydroelectric power to the total ecosystem service benefits. We used this approach in a case study of the Three Gorges Reservoir, the world’s largest reservoir, which provides multiple ecosystem services. We found large differences between the WFh and the water footprint of per unit of hydroelectric production (PWFh) calculated using ηh and those calculated without this factor. From 2003 to 2012, ηh decreased sharply (from 0.76 in 2005 to 0.41 in 2012), which was due to the fact that large increases in the value of non-energy ecosystem services, and particularly flood control. In 2009, flood control replaced hydroelectricity as the largest ecosystem service of water from the Three Gorges Reservoir. Using our approach, WFh and PWFh averaged 331.0 × 106 m3 and 1.5 m3 GJ−1, respectively. However, these values would almost double without allocating water footprints among different reservoir ecosystem services. Thus, previous studies have overestimated the WFh and PWFh of reservoirs, especially for reservoirs that serve multiple purposes. Thus, the allocation coefficient should not be ignored when calculating the WF of a product or service.  相似文献   

19.
Bezafibrate (BZF), a widely used lipid regulator, is a potential threat to ecosystems and human health in water, and the recent research showed that advanced oxidation processes (AOPs) are much more effective for BZF degradation. In this study, we investigated the photochemical decomposition of BZF in surface water and effluent from waste water treatment plants (WWTP) by UV/H2O2 process. The results showed that the UV/H2O2 process was a promising method to remove BZF at low concentration, generally at µg L?1 level. When initial concentrations reach 100 µg L?1 in the deionized water, >99.8% of BZF could be removed in 16 min under UV intensity of 61.4 µm cm?2, at the H2O2 concentration of 0.1 mg L?1, and neutral pH condition. Moreover, BZF degradation was inhibited in this process when humic acid (HA) and inorganic solution anions were added to the deionized water solutions, including chloride, nitrate, bicarbonate, and sulfate, significantly. In the surface water and effluent of WWTP, however, the removal efficiency of BZF was lower than that in the deionized water because of the interference of complex constituents in the surface water and effluent. Some main intermediates at the m/z range of 100–400 were observed by high performance LC‐MS (HPLC/MS) and a simple pathway of BZF degradation by UV/H2O2 was proposed.  相似文献   

20.
自成库以来,三峡水库CO2、CH4等温室气体通量较蓄水前发生明显改变。如何科学认识和客观评估三峡水库修建及运行对其CO2、CH4等温室气体通量的影响备受关注。本文简要回顾了自2009年以来在三峡水库开展CO2、CH4等温室气体通量监测与分析工作,综述认为,现阶段三峡水库温室气体排放以水-气界面扩散释放为主要途径。陆源输入的有机碳是主导三峡水库CO2、CH4产生的主要碳源,但在局部区段或时段自源性有机碳的贡献亦十分显著。同蓄水前相比,三峡水库碳排放量呈现为净增加,淹没效应约占水库C净增量的20%,库区内点面源污染负荷并未对CO2排放的净增量产生显著贡献,阻隔效应和生态系统重建效应对三峡水库碳排放的净增量产生显著贡献。近10年来,监测方法比对、监测点位优化等工作在一定程度上完善了三峡水库温室气体通量监测体系。新方法、新技术的引入也为三峡水库温室气体通量监测分析提供了有利支撑和保障,但复杂水文环境...  相似文献   

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