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1.
The impact of landfill contaminated groundwater along a reach of a small stream adjacent to a municipal landfill was investigated using stable carbon isotopes as a tracer. Groundwater below the stream channel, groundwater seeping into the stream, groundwater from the stream banks and stream water were sampled and analysed for dissolved inorganic carbon (DIC) and the isotope ratio of DIC (δ13CDIC). Representative samples of groundwater seeping into the stream were collected using a device (a ‘seepage well’) specifically designed for collecting samples of groundwater seeping into shallow streams with soft sediments. The DIC and δ13CDIC of water samples ranged from 52 to 205 mg C/L and ?16·9 to +5·7‰ relative to VPDB standard, respectively. Groundwater from the stream bank adjacent to the landfill and some samples of groundwater below the stream channel and seepage into the stream showed evidence of δ13C enriched DIC (δ13CDIC = ?2·3 to +5·7‰), which we attribute to landfill impact. Stream water and groundwater from the stream bank opposite the landfill did not show evidence of landfill carbon (δ13CDIC = ?10·0 to ?16·9‰). A simple mixing model using DIC and δ13CDIC showed that groundwater below the stream and groundwater seeping into the stream could be described as a mixture of groundwater with a landfill carbon signature and uncontaminated groundwater. This study suggests that the hyporheic zone at the stream–groundwater interface probably was impacted by landfill contaminated groundwater and may have significant ecological implications for this ecotone. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

2.
ABSTRACT

This study aims to differentiate the potential recharge areas and flow mechanisms in the North-eastern Basin, Palestine. The results differentiate the recharge into three main groups. The first is related to springs and some of the deep wells close to the Anabta Anticline, through the Upper Aquifer (Turonian) formation, with depleted δ18O and δ2H. The second is through the Upper Cenomanian formation surrounding the Rujeib Monocline in the southeast, where the lineament of the Faria Fault plays an important role, with relatively enriched δ13CDIC values of about ?4‰ (VPDB). The third is the Jenin Sub-series, which shows higher δ13CDIC values, with enriched δ18O and δ2H and more saline content. The deep wells from the Nablus area in the south of the basin indicate low δ13CDIC values due to their proximity to freshwater infiltrating faults. The deep wells located to the northwest of the basin have δ13CDIC values from ?8 to ?9‰ (VPDB), with enriched δ18O signatures, indicating slow recharge through thick soil.  相似文献   

3.
We measured the concentrations of dissolved inorganic carbon (DIC) and major ions and the stable carbon isotope ratios of DIC (δ13CDIC) in two creeks discharging from carbonate‐rich sulphide‐containing mine tailings piles. Our aim was to assess downstream carbon evolution of the tailings discharge as it interacted with the atmosphere. The discharge had pH of 6.5–8.1 and was saturated with respect to carbonates. Over the reach of one creek, the DIC concentrations decreased by 1.1 mmol C/l and δ13CDIC increased by ~4.0‰ 200 m from the seep source. The decrease in the DIC concentrations was concomitant with decreases in the partial pressure of CO2(aq) because of the loss of excess CO2(aq) from the discharge. The corresponding enrichment in the δ13CDIC is because of kinetic isotope fractionation accompanying the loss of CO2(g). Over the reach of the other creek, there was no significant decrease in the DIC concentrations or notable changes in the δ13CDIC. The insignificant change in the DIC concentrations and the δ13CDIC is because the first water sample was collected 160 m away from the discharge seep, not accessible during this research. In this case, most of the excess CO2(aq) was lost before our first sampling station. Our results indicate that neutral discharges from tailings piles quickly lose excess CO2(aq) to the atmosphere and the DIC becomes enrich in 13C. We suggest that a significant amount of carbon cycling in neutral discharges from tailings piles occur close to the locations where the discharge seeps to the surface. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

4.
Globally, dissolved inorganic carbon (DIC) accounts for more than half the annual flux of carbon exported from terrestrial ecosystems via rivers. Here, we assess the relative influences of biogeochemical and hydrological processes on DIC fluxes exported from a tropical river catchment characterized by distinct land cover, climate and geology transition from the wet tropical mountains to the low‐lying savanna plains. Processes controlling changes in river DIC were investigated using dissolved organic carbon, particulate organic carbon and DIC concentrations and stable isotope ratios of DIC (δ13CDIC) at two time scales: seasonal and diel. The recently developed Isotopic Continuous Dissolved Inorganic Carbon Analyser was used to measure diel DIC concentration and δ13CDIC changes at a 15‐min temporal resolution. Results highlight the predominance of biologically mediated processes (photosynthesis and respiration) controlling diel changes in DIC. These resulted in DIC concentrations varying between 3.55 and 3.82 mg/l and δ13CDIC values ranging from ?19.7 ± 0.31‰ to ?17.1 ± 0.08‰. In contrast, at the seasonal scale, we observed wet season DIC variations predominantly from mixing processes and dry season DIC variations due to both mixing processes and biological processes. The observed wet season increases in DIC concentrations (by 6.81 mg/l) and δ13CDIC values of river water (by 5.4‰) largely result from proportional increases in subsurface inflows from the savanna plains (C4 vegetation) region relative to inflows from the rainforest (C3 vegetation) highlands. The high DIC river load during the wet season resulted in the transfer of 97% of the annual river carbon load. Therefore, in this gaining river, there are significant seasonal variations in both the hydrological and carbon cycles, and there is evidence of substantial coupling between the carbon cycles of the terrestrial and the fluvial environments. Recent identification of a substantial carbon sink in the savannas of northern Australia during wetter years in the recent past does not take into account the possibility of a substantial, rapid, lateral flux of carbon to rivers and back to the atmosphere. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

5.
Major inorganic ions and stable carbon and oxygen isotopes in stream water, groundwater, groundwater seeps and springs were measured in the Corral Canyon meadow complex and watershed in the Toquima Mountains of central Nevada, USA. The purpose of the study was to determine whether stream water or groundwater was the source of water that supports vegetation in the meadow complex. Water samples from the watershed and meadow complex were mixed cation–HCO3 type. Stream water sampled at different locations in the meadow complex showed variations in temperature, pH and specific conductance. The cation–anion proportions for stream water were similar to groundwater, groundwater seeps and runoff from the meadow complex. Stable oxygen isotope ratios for stream water (?17·1 to ?17·6‰ versus VSMOW) and groundwater and groundwater seeps in the meadow site (?17·0 to ?17·7‰ versus VSMOW) were similar, and consistent with a local meteoric origin. Dissolved inorganic carbon (DIC) and the δ 13CDIC for stream water (?12·1 to ?15·0‰ versus VPDB) were different from that of groundwater from the meadow complex (?15·3 to ?19·9‰ versus VPDB), suggesting different carbon evolution pathways. However, a simple model based on cation–δ 13CDIC suggests that stream water was being recharged by shallow groundwater, groundwater seeps and runoff from the meadow complex. This leads to the conclusion that the source of water that supports vegetation in the meadow complex was primarily groundwater. The results of this study suggest that multiple chemical and stable carbon isotope tracers are useful in determining the source of water that supports vegetation in meadow complexes in small alpine watersheds. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

6.
In regions where aquifers sustain rivers, the location and quantification of groundwater discharge to surface water are important to prevent pollution hazards, to quantify and predict low flows and to manage water supplies. 222Rn is commonly used to determine groundwater discharge to rivers. However, using this isotopic tracer is challenging because of the high diffusion capacity of 222Rn in open water. This study illustrates how a combination of isotopic tracers can contribute to an enhanced understanding of groundwater discharge patterns in small rivers. The aim of this paper is to combine 222Rn and δ13CDIC to better constrain the physical parameters related to the degassing process of these tracers in rivers. The Hallue River (northern France) was targeted for this study because it is sustained almost exclusively by a fractured chalk aquifer. The isotopes 222Rn, δ13CDIC, δ2H and δ18O were analysed along with other natural geochemical tracers. A mass balance model was used to simulate 222Rn and δ13CDIC. The results of δ2H and δ18O analyses prove that evaporation did not occur in the river. The calibration of a numerical model to reproduce 222Rn and δ13CDIC provides a best‐fit diffusive layer thickness of 3.21 × 10?5 m. This approach is particularly useful for small rivers flowing over carbonate aquifers with high groundwater DIC where the evolution of river DIC reflects the competing processes of groundwater inflow and CO2 degassing. This approach provides a means to evaluate groundwater discharge in small ungauged rivers. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

7.
Dissolved inorganic carbon (DIC) is the most important carbon component in karst aquatic system where fluid is highly transmissive, but has rarely been examined in the subtropical karst critical zone (K-CZ). In this study, concentrations of dissolved solutes and isotopic compositions of DIC (δ13CDIC) at 11 sites of a 73.4 km2 karstic catchment in Southwestern China were analysed monthly in order to uncover the spatiotemporal variations of both DIC and its dominant sources, and to identify relevant controlling factors. Both DIC concentrations and δ13CDIC were highly variable, ranging from 2.52 to 5.85 mmol l−1 and from −15.7 to −4.5‰, respectively. DIC in underground water (UGW) was higher in concentration and more depleted in 13C compared to surface water (SFS). DIC concentrations showed an inconsistent seasonal trend with other solutes, with higher values in the wet season at some sites. δ13CDIC values were lower in the wet season than in the dry season. The results of mixing model IsoSource revealed spatiotemporal patterns of DIC sources. During the dry season, carbonate weathering was the primary contributor to DIC in UGW (excluding in the middle reaches). However, during the wet season, soil CO2 was the dominant source of DIC in both UGW and SFS, and it was higher than in the dry season. Overall, there are significant spatiotemporal disparities and highly transmissive characteristics of both DIC and its sources in the K-CZ, which are controlled by multiple factors. This study also highlights that rainfall may play a crucial role in accelerating carbon dynamics in the K-CZ. High-frequency sampling campaigns in high-flow periods and deep analyses are needed in future work to elucidate the related processes and mechanisms. © 2019 John Wiley & Sons, Ltd.  相似文献   

8.
The origin and the chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta in semi-arid Botswana were investigated using DIC and major ion concentrations and stable oxygen, hydrogen and carbon isotopes (δD, δ18O and δ13CDIC). The δD and δ18O indicated that groundwater was recharged by evaporated river water and unevaporated rain. The river water and shallow (<10 m) groundwater are Ca–Na–HCO3 type and the deep (≥10 m) groundwater is Na–K–HCO3 to HCO3–Cl–SO4 to Cl–SO4–HCO3. Compared to river water, the mean DIC concentrations were 2 times higher in shallow groundwater, 7 times higher in deep groundwater and 24 times higher in island groundwater. The δ13CDIC indicate that DIC production in groundwater is from organic matter oxidation and in island groundwater from organic matter oxidation and dissolution of sodium carbonate salts. The ionic and isotopic evolution of the groundwater relative to evaporated river water indicates two independent pools of DIC.  相似文献   

9.
The Nyangqu River, the largest right bank tributary of the Yarlung Zangbo River in the Qinghai–Tibet Plateau, was representative of an alpine riverine carbon cycle experiencing climate change. In this study, dissolved inorganic carbon (DIC) spatial and seasonal variations, as well as their carbon isotopic compositions (δ13CDIC) in river water and groundwater were systematically investigated to provide constraints on DIC sources, recharge and cycling. Significant changes in the δ13CDIC values (from −2.9‰ to −23.4‰) of the water samples were considered to be the result of different contributions of two dominant DIC origins: soil CO2 dissolution and carbonate weathering. Three types of rock weathering (dissolution of carbonate minerals by H2CO3 and H2SO4, and silicate dissolution by H2CO3) were found to control the DIC input into the riverine system. In DIC cycling, groundwater played a significant role in delivering DIC to the surface water, and DIC supply from tributaries to the main stream increased from the dry season to the wet season. Notably, the depleted δ13CDIC ‘peak’ around the 88.9° longitude, especially in the September groundwater samples, indicated the presence of ‘special’ DIC, which was attributed to the oxidation of methane from the Jiangsa wetland located nearby. This wetland could provide large amounts of soil organic matter available for bacterial degradation, producing 13C-depleted methane. Our study provided insights regarding the role of wetlands in riverine carbon cycles and highlighted the contribution of groundwater to alpine riverine DIC cycles.  相似文献   

10.
The hydrology of oxygen‐18 (18O) isotopes was monitored between 1995 and 1998 in the Allt a' Mharcaidh catchment in the Cairngorm Mountains, Scotland. Precipitation (mean δ18O=−7·69‰) exhibited strong seasonal variation in δ18O values over the study period, ranging from −2·47‰ in the summer to −20·93‰ in the winter months. As expected, such variation was substantially damped in stream waters, which had a mean and range of δ18O of −9·56‰ and −8·45 to −10·44‰, respectively. Despite this, oxygen‐18 proved a useful tracer and streamwater δ18O variations could be explained in terms of a two‐component mixing model, involving a seasonally variable δ18O signature in storm runoff, mixing with groundwater characterized by relatively stable δ18O levels. Variations in soil water δ18O implied the routing of depleted spring snowmelt and enriched summer rainfall into streamwaters, probably by near‐surface hydrological pathways in peaty soils. The relatively stable isotope composition of baseflows is consistent with effective mixing processes in shallow aquifers at the catchment scale. Examination of the seasonal variation in δ18O levels in various catchment waters provided a first approximation of mean residence times in the major hydrological stores. Preliminary estimates are 0·2–0·8 years for near‐surface soil water that contributes to storm runoff and 2 and >5 years for shallow and deeper groundwater, respectively. These 18O data sets provide further evidence that the influence of groundwater on the hydrology and hydrochemistry of upland catchments has been underestimated. Copyright © 2000 John Wiley & Sons, Ltd.  相似文献   

11.
Spatial and temporal patterns of spring break‐up flooding in the Slave River Delta (SRD), Northwest Territories, are characterized during three years (2003–2005) using water isotope tracers and total inorganic suspended sediment (TSS) concentrations measured from lakewater samples collected shortly after the spring melt. Strongly contrasting spring melt periods led to a moderate flood in 2003, no flooding in 2004 and widespread flooding in 2005. Flooded lakes have isotopically‐depleted δ18O (δ2H) signatures, ranging between ? 19·2‰ (?145‰) and ? 17·1‰ (?146‰) and most have high TSS concentrations (>10 mg L?1), while non‐flooded lakes have more isotopically‐enriched δ18O (δ2H) signatures, ranging between ? 18·2‰ (?149‰) and ? 10·6‰ (?118‰) and low TSS concentrations (<10 mg L?1). These results, in conjunction with the isotopic signatures of Slave River water and snowmelt, are used to estimate the proportion of river‐ or snowmelt‐induced dilution in delta lakes during the spring of each study year. Calculations indicate river flooding caused dilution of ～70–100% in delta lakes, while snowmelt dilution in the absence of river flooding ranged from ～0–56%. A positive relationship exists between the spatial extent of spring flooding in the SRD and level and discharge on the Slave River and upstream tributaries, suggesting that upstream flow generation plays a key role in determining the magnitude of spring flooding in the SRD. Parallel variations in the 46‐year instrumental Slave River discharge record and flood stratigraphy in the active delta indicate that there is potential for extending the flood history of the SRD, a development that will contribute to a more robust understanding of the drivers of historic, contemporary and future flood frequency in the delta. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

12.
This paper focuses on the chemical and isotopic features of dissolved gases (CH4 and CO2) from four meromictic lakes hosted in volcanic systems of Central–Southern Italy: Lake Albano (Alban Hills), Lake Averno (Phlegrean Fields), and Monticchio Grande and Piccolo lakes (Mt. Vulture). Deep waters in these lakes are characterized by the presence of a significant reservoir of extra-atmospheric dissolved gases mainly consisting of CH4 and CO2. The δ13C-CH4 and δD-CH4 values of dissolved gas samples from the maximum depths of the investigated lakes (from ?66.8 to ?55.6?‰ V-PDB and from ?279 to ?195?‰ V-SMOW, respectively) suggest that CH4 is mainly produced by microbial activity. The δ13C-CO2 values of Lake Grande, Lake Piccolo, and Lake Albano (ranging from ?5.8 to ?0.4?‰ V-PDB) indicate a significant CO2 contribution from sublacustrine vents originating from (1) mantle degassing and (2) thermometamorphic reactions involving limestone, i.e., the same CO2 source feeding the regional thermal and cold CO2-rich fluid emissions. In contrast, the relatively low δ13C-CO2 values (from ?13.4 to ?8.2?‰ V-PDB) of Lake Averno indicate a prevalent organic CO2. Chemical and isotopic compositions of dissolved CO2 and CH4 at different depths are mainly depending on (1) CO2 inputs from external sources (hydrothermal and/or anthropogenic); (2) CO2–CH4 isotopic exchange; and (3) methanogenic and methanotrophic activity. In the epilimnion, vertical water mixing, free oxygen availability, and photosynthesis cause the dramatic decrease of both CO2 and CH4 concentrations. In the hypolimnion, where the δ13C-CO2 values progressively increase with depth and the δ13C-CH4 values show an opposite trend, biogenic CO2 production from CH4 using different electron donor species, such as sulfate, tend to counteract the methanogenesis process whose efficiency achieves its climax at the water–bottom sediment interface. Theoretical values, calculated on the basis of δ13C-CO2 values, and measured δ13CTDIC values are not consistent, indicating that CO2 and the main carbon-bearing ion species (HCO3 ?) are not in isotopic equilibrium, likely due to the fast kinetics of biochemical processes involving both CO2 and CH4. This study demonstrates that the vertical patterns of the CO2/CH4 ratio and of δ13C-CO2 and δ13C-CH4 are to be regarded as promising tools to detect perturbations, related to different causes, such as changes in the CO2 input from sublacustrine springs, that may affect aerobic and anaerobic layers of meromictic volcanic lakes.  相似文献   

13.
The stable isotope composition (18O and 2H) in the tropical precipitation collected from 18 locations throughout the Deduru Oya river basin in Sri Lanka, has been studied during August and September 2001, in order to characterize the isotopic composition of precipitation in the dry and intermediate climatic zones of Sri Lanka. The isotope compositions are described with respect to the distance from the coast and the altitude. The analyses show that δ18O vary from ? 5·11 to 1·39‰ and δD vary from ? 35·71 to 12·55‰. The d‐excess values range from ? 0·65 to 13·17 with an average value of ～7. Regression for the δ18O ? δD is y = 6·8x + 4·9 (R2 = 0·9) which is compatible with the precipitation in other tropical regions. The lower slope in the regression line and the lower d‐excess value indicate high temperature events which were possibly aided by concentration through successive evaporation within the atmosphere. The spatial variation of isotope composition indicates two different cloud contributions for the rain events, of which one may be linked to the Indian Ocean contribution and the other to the high altitude condensation. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

14.
According to the precipitation and δ18O data obtained during the GEWEX Asian Monsoon Experiment–Tibet Intensive Observation Period, based on the knowledge that δ18O is lower in precipitation formed from ocean air mass vapour than that from local evaporation vapour, the water vapour sources can be identified from the δ18O values in precipitation. We attempt to give the identification criterion of δ18O values in precipitation. The threshold values chosen to distinguish between ocean and local sources are δ18O < ?20‰ and δ18O > ?13‰ respectively. According to this criterion, the proportion of local evaporation‐formed precipitation and ocean air‐mass‐formed precipitation in total precipitation was estimated. The average value of precipitation at three sites (NODA, Amdo and AQB) is 249·76 mm. Among this, precipitation formed directly by the ocean air mass vapour is 80·08 mm at most. Precipitation formed by water vapour evaporated from local places is 117·05 mm at least. That is to say that precipitation formed directly by the ocean air mass vapour accounts for 32·06% of the total precipitation at most. Precipitation formed by water vapour evaporated from local places accounts for 46·86% of the total precipitation at least. At least 21·8% of the total precipitation came from water vapour that was evaporated on the way and transported by the monsoon circulation. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

15.
Aquatic plants are essential for maintaining the diversity and stability of a lake ecosystem. Stable carbon isotopes (δ13C) of macrophytes have been widely used as a powerful tool to study ecological processes and paleoenvironmental evolution in lakes. Varying results are obtained when using the δ13C of macrophytes to study the changes in the lake environment at different spatio-temporal scales. Thus, sample preparation and subsequent laboratory analyses are crucial for studying environmental changes using the isotopic signal retained in the macrophytes, and are essential for the interpretation of isotope-environment relationships. This study analyzed the δ13C of different tissue components of macrophytes in three lakes of the lower Yangtze River basin, and a correlation analysis was performed on aquatic environments influencing the δ13C values in the different tissue components of macrophytes. The test results showed the difference between the δ13C values of the whole sample and cellulose. Relative analyses indicated that the major factors contributing to the δ13C variability in macrophytes were pH and the concentration of dissolved inorganic carbon (DIC). The δ13C of α-cellulose (δ13CAC) is more sensitive to environmental variables than that of the whole sample (δ13CW) and holocellulose (δ13CHC). The results of this study imply that extraction of α-cellulose is a prerequisite for research on the changes in lake environment using δ13C of macrophytes. This study aims to provide theoretical and data basis for further research on the environmental and ecological change using stable carbon isotopes of aquatic plants.  相似文献   

16.
Zeyong Gao  Fujun Niu  Zhanju Lin 《水文研究》2020,34(26):5659-5673
Thermokarst lakes play a key role in the hydrological and biogeochemical cycles of permafrost regions. Current knowledge regarding the changes caused by permafrost degradation to the hydrochemistry of lakes in the Qinghai-Tibet Plateau (QTP) is limited. To address this gap, a systematic investigation of thermokarst lake water, suprapermafrost water, ground ice, and precipitation was conducted in the hinterland of the QTP. The thermokarst lake water in the QTP was identified to be of the Na-HCO3-Cl type. The mean concentrations of HCO3− and Na+ were 281.8 mg L−1 (146.0–546.2 mg L−1) and 73.3 mg L−1 (9.2–345.8 mg L−1), respectively. The concentrations of Li+, NH4+, K+, F−, NO2−, and NO3− were relatively low. Freeze-out fractionation concentrated the dissolved solids within the lake water during winter, which was deeply deepened on lake depth and lake ice thickness. Owing to solute enrichment, the ground ice was characterized by high salinity. Conversely, repeated replenishment via precipitation led to lower solute concentrations in the ground ice near the permafrost table compared to that within the permafrost. Although lower solute concentration existed in precipitation, the soil leaching and saline ground ice melting processes enhanced the solute load in suprapermafrost water, which is considered an important water and solute resource in thermokarst lakes. The influencing mechanism of permafrost degradation on thermokarst lake hydrochemistry is presumably linked to: (1) the liberation of soluble materials sequestered in ground ice; (2) the increase of solutes in suprapermafrost water and soil pore water; and (3) the changes in lake morphometry. These results have major implications on the understanding of the effects of ground ice melting on ecosystem functions, biogeochemical processes, and energy balance in a rapidly changing climate.  相似文献   

17.
Water is a limiting factor for life in the McMurdo Dry Valleys (MDV), Antarctica. The active layer (seasonally thawed soil overlying permafrost) accommodates dynamic hydrological and biological processes for 10–16 weeks per year. Wetted margins (visually wetted areas with high moisture content) adjacent to lakes and streams are potential locations of great importance in the MDV because of the regular presence of liquid water, compared with the rest of the landscape where liquid water is rare. At 11 plots (four adjacent to lakes, seven adjacent to streams), soil particle size distribution, soil electrical conductivity, soil water content and isotopic signature, width of the wetted margin, and active layer thaw depth were characterised to determine how these gradients influence physicochemical properties that determine microbial habitat and biogeochemical cycling. Sediments were generally coarse‐grained in wetted margins adjacent to both lakes and streams. Wetted margins ranged from 1·04 to 11·01 m in average length and were found to be longer at lakeside sites than streamside. Average thaw depths ranged from 0·12 to 0·85 m, and were found to be deepest under lake margins. Lake margins also had much higher soil electrical conductivity, steeper topographic gradients, but more gradual soil moisture gradients than stream margins. Patterns of soil water δ18O and δD distribution indicate capillary action and evaporation from wetted margins; margin pore waters generally demonstrated isotopic enrichment with distance from the shore, indicating evaporation of soil water. Lake margin pore waters were significantly more negative in DXS (DXS = δD‐8δ18O) than streamside pore waters, indicating a longer history of evaporation there. Differences between lake and stream margins can be explained by the more consistent availability of water to lake margins than stream margins. Differences in margin characteristics between lakes and streams have important consequences for the microbial habitat of these margins and their functional role in biogeochemical cycling at these terrestrial–aquatic interfaces. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

18.
The stable isotopic composition of dissolved inorganic carbon (δ13C‐DIC) was investigated as a potential tracer of streamflow generation processes at the Sleepers River Research Watershed, Vermont, USA. Downstream sampling showed δ13C‐DIC increased between 3–5‰ from the stream source to the outlet weir approximately 0·5 km downstream, concomitant with increasing pH and decreasing PCO2. An increase in δ13C‐DIC of 2·4 ± 0·1‰ per log unit decrease of excess PCO2 (stream PCO2 normalized to atmospheric PCO2) was observed from downstream transect data collected during snowmelt. Isotopic fractionation of DIC due to CO2 outgassing rather than exchange with atmospheric CO2 may be the primary cause of increased δ13C‐DIC values downstream when PCO2 of surface freshwater exceeds twice the atmospheric CO2 concentration. Although CO2 outgassing caused a general increase in stream δ13C‐DIC values, points of localized groundwater seepage into the stream were identified by decreases in δ13C‐DIC and increases in DIC concentration of the stream water superimposed upon the general downstream trend. In addition, comparison between snowmelt, early spring and summer seasons showed that DIC is flushed from shallow groundwater flowpaths during snowmelt and is replaced by a greater proportion of DIC derived from soil CO2 during the early spring growing season. Thus, in spite of effects from CO2 outgassing, δ13C of DIC can be a useful indicator of groundwater additions to headwater streams and a tracer of carbon dynamics in catchments. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

19.
CO2-rich inclusions recovered from “popping” and related tholeiitic rocks from the Mid-Atlantic Ridge have δ13C values of ?7.6 ± 0.5%. relative to PDB. δ13C values of total carbon in the same rocks range from ?12 to ?13.7‰. These values are discussed in the light of the known δ13C variations in rocks of deep-seated origin. The ?7.6‰ value is interpreted as a reasonable estimate of the primary value of δ13C of deep-seated carbon in the ridge area.  相似文献   

20.
The use of stable isotopes is a practical tool in the study of the lake water budget. This is an one way to study the hydrological cycle in the large numbers of inland lakes on the Tibetan Plateau, in which the isotope record of the sediment is believed to reflect the climatic and environmental changes. The monitoring of stable isotopes of the precipitation, river and lake waters during 2004 in the inland Yamdruk‐tso basin, southern Tibetan Plateau, reveals the lake water δ18O is over 10‰ higher than the local precipitation. This high difference indicates strong isotope enrichment due to lake water evaporation. The simulation results based on the isotope technique show that the present lake water δ18O level corresponds to an average relative humidity of around 54–58% during evaporation, which is very close to the instrumental observation. The simulation results also show that the inland lakes on the Tibetan Plateau have a strong adjustability to the isotope shift of input water δ18O. On average, the isotope component in the inland lake water is to a large extent controlled by the local relative humidity, and can also be impacted by a shift of the local precipitation isotope component. This is probably responsible for the large consistence in the isotope component in the extensive inland lakes on the Tibetan Plateau. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

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