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1.
Mass balance calculations and hydrodynamics of groundwater flow suggest that the solutes in brines of the coastal sabkha aquifer from the Emirate of Abu Dhabi are derived largely from ascending geologic brines into the sabkha from the underlying formations. Solute interpretation for the ascending brine model (ABM) was based on two independent but secondary lines of evidence (solute ratios and solute fluxes). In the current study, direct primary evidence for this ABM was provided through analyses of δ81Br, δ37Cl, and 87Sr/86Sr. Different solute histories of geologic brine and sea water provide an “isotopic fingerprint” that can uniquely distinguish between the two possible sources. Samples from the coastal sabkha aquifer of Abu Dhabi were determined to have a mean δ81Br of 1.17‰ that is statistically equal, at the 95% confidence level, to the mean of 1.11‰ observed in the underlying geologic brine and statistically different than sea water. Similarly, the δ37Cl in sabkha brine has a mean of 0.25‰ and is statistically equal to a mean of 0.21‰ in the underlying geologic brines at the 95% confidence level and statistically different from sea water. Also, dissolved strontium isotope data are consistent with the ABM and even with the complex set of processes in the sabkha, the variance in strontium isotope results is similar to the geologic brine. These observations provide primary direct evidence consistent that the major source of these solutes (and presumably others in the aquifer) is from discharging geologic brines, not from adjacent sea water.  相似文献   

2.
Oxygen and hydrogen isotopes were used in this study to detect a hydraulic connection between a sinkhole lake and a karst spring. In karst areas, surface water that flows to a lake can drain through sinkholes in the lakebed to the underlying aquifer, and then flows in karst conduits and through aquifer matrix. At the study site located in northwest Florida, USA, Lake Miccosukee immediately drains into two sinkholes. Results from a dye tracing experiment indicate that lake water discharges at Natural Bridge Spring, a first-magnitude spring 32 km downgradient from the lake. By collecting weekly water samples from the lake, the spring, and a groundwater well 10 m away from the lake during the dry period between October 2019 and January 2020, it was found that, when rainfall effects on isotopic signature in spring water are removed, increased isotope ratios of spring water can be explained by mixing of heavy-isotope-enriched lake water into groundwater, indicating hydraulic connection between the lake and the spring. Such a detection of hydraulic connection at the scale of tens of kilometers and for a first-magnitude spring has not been previously reported in the literature. Based on the isotope ratio data, it was estimated that, during the study period, about 8.5% the spring discharge was the lake water that drained into the lake sinkholes.  相似文献   

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5.
This study investigates water vapor isotopic patterns and controls over China using high-quality water vapor δD data retrieved from the Scanning Imaging Absorption Spectrometer for Atmospheric Chartography(SCIAMACHY) observations.The results show that water vapor δD values on both annual and seasonal time-scales broadly exhibit a continental effect,with values largely decreasing northwestward from coastal lowlands to high-elevation mountainous regions.However,region-specific analysis reveals spatially distinct patterns of water vapor δD between seasons.In the monsoon domain(e.g.,China south of 35°N),depletion in D in the summer and fall seasons is closely tied to monsoon moisture sources(the Indian and Pacific oceans) and subsequent amount effect,but higher δD values in winter and spring are a result of isotopically-enriched continental-sourced moisture proceeded by less rainout.In contrast,farther inland in China(non-monsoon domain),moisture is derived overwhelmingly from the dry continental air masses and local evaporation,and δD values are largely controlled by the temperature effect,exhibiting a seasonality with isotopically enriched summer and depleted winter/spring.The observation that the spatial pattern of water vapor δD is the opposite to that of precipitation δD in the summer season also suggests that partial evaporation of falling raindrops is a key driver of water vapor isotope in the non-monsoon domain.This study highlights the importance of non-Rayleigh factors in governing water vapor isotope,and provides constraints on precipitation isotope interpretation and modern isotope hydrological processes over China.  相似文献   

6.
The impact on groundwater imparted by the infiltration of high dissolved organic carbon (DOC) leachate from capped, unlined landfills can be attenuated by biogeochemical reactions beyond the waste source, although such reactive loss in the aquifer is difficult to distinguish from conservative advective dispersion. Compound-specific measurement of δ(13)C in carbon species, including CH(4), dissolved inorganic carbon (DIC), and the major DOC compounds (acetate, humic acid, and fulvic acid) provides a constraint in this assessment that can assist in exercises of modeling and prediction of leachate transport. The Trail Road municipal landfill near Ottawa, Ontario, Canada, hosts an unlined sector which produces a highly enriched leachate (DOC >4500 mg/L) that provides a good site to examine reactive attenuation within the receptor aquifer. Acetate, a sentinel component of leachate DOC (~1000 mg C/L), is absent in impacted groundwater. Mass balance calculations together with reaction modeling suggest continued acetate fermentation with calcite control on DIC and δ(13)C(DIC) evolution. In groundwater within 50 m of the landfill, methane concentrations are elevated (~10 mg/L), consistent with acetate fermentation, whereas δ(13)C(CH4) measurements in deeper groundwater range down to -51‰ compared with -60‰ in the landfill demonstrating oxidative loss. DOC in the deep aquifer is remarkably depleted to values less than -40‰ suggesting methanotrophic bacteria selectively consume isotopically light CH(4) to fix carbon. Continued reaction of leachate DOC in groundwater is demonstrated by evolution away from conservative mixing lines on diagrams of δ(13)C vs. concentrations of DIC and DOC.  相似文献   

7.
The natural abundance of 15N (δ15N) has been widely used to detect anthropogenically derived N loads in environmental impact studies. The present study involved retrospective analysis of subsamples of Fucus vesiculosus L. collected during a period of three years (2008–2010) from two sites: a control site, within a coastal reference area, and an area affected by the effluents of a marine land-based fish farm. The isotopic signal in different subsamples of the macroalgae thalli (tissue that has grown during the same period) varied depending on the age of the tissue. Moreover, the isotopic signal decreased significantly with the age of the frond to within a certain range. The δ15N of F. vesiculosus is temporally unstable; therefore, measurement of the δ15N of macroalgal tissues does not allow reliable retrospective biomonitoring of environmental pollution. Further knowledge about the growth and other biological aspects of this species is required.  相似文献   

8.
Biomagnification profiles of polycyclic aromatic hydrocarbons (PAHs), alkylphenols, and polychlorinated biphenyls (PCBs) from the innermost part of Tokyo Bay, Japan were analyzed using stable carbon (δ13C) and nitrogen (δ15N) isotope ratios as guides to trophic web structure. δ15N analysis indicated that all species of mollusks tested were primary consumers, while decapods and fish were secondary consumers. Higher concentrations of PCBs occurred in decapods and fish than in mollusks. In contrast, concentrations of PAHs and alkylphenols were lower in decapods and fish than in mollusks. Unlike PCBs, whose concentrations largely increased with increasing δ15N (i.e. increasing trophic level), all PAHs and alkylphenols analyzed followed a reverse trend. Molecular weights of PAHs are lower than those of PCBs, therefore low membrane permeability caused by large molecular size is an unlikely factor in the “biodilution” of PAHs. Organisms at higher trophic levels may rapidly metabolize PAHs or they may assimilate less of them.  相似文献   

9.
During the 22nd Chinese Antarctic Research Expedition (CHINARE-22), the atmospheric gas samples above the oceanic surface and near the surface were collected on the track for the scientific ship "Xuelong" and on Millor Peninsula of eastern Antarctica, respectively, using the Tedlar gas bags. Every day the sampling times were 10:00 and 22:00 (local time), respectively. In the laboratory, high-precision measurement of the isotopic compositions for N2O in these gas samples was conducted using Thermo Finnigan MAT-253 Isotopic Mass Spectrometer with a fully automated interface for the pre-GC concen-tration (PreCon) of trace gases. The temporal and spatial variations of δ 15N and δ 18O in atmospheric N2O were analyzed. The mean δ 15N and δ 18O-N2O values above the oceanic surface were (7.21±0.50)‰ and (44.52±0.52)‰, respectively. From 30°N to Antarctica, the δ 15N (6.05‰―7.88‰) linearly increased with the rate of about 0.01‰ with the latitude while the δ 18O (43.05‰―48.78‰) showed a large fluctua-tion. The δ 15N negatively correlated with air temperature and N2O concentration, and slightly positively correlated with δ 18O. The summertime variations of δ 15N and δ 18O-N2O appeared the same trend on Millor Peninsula of eastern Antarctica. They significantly positively correlated with each other and negatively with N2O concentration. The δ 15N and δ 18O-N2O at different sites averaged (7.42±0.35)‰ and (44.69±0.49)‰, respectively, slightly higher than those above the oceanic surface, significantly higher than those of atmospheric N2O in the low-latitude regions of Northern Hemisphere. The predominant factors affecting the spatial variations of δ 15N and δ 18O values were also discussed. The isotopic data given in this study can help to investigate the global and regional N2O budgets.  相似文献   

10.
In-situ seasonalδ18O measurements of section 236.3–235.6 cm of speleothem HS4,from Qingjiang Valley of the Middle reaches of Yangtze River,China,were performed by an Secondary Ionization Mass Spectrometry(SIMS)with Oka(Chinese primary calcite standard GBW04481)and UWC-3(international calcite standard from University of Wisconsin).The potential of using SIMSδ18O measurements to establish speleothem time series has been explored and the differences between conventional and SIMSδ18O values have been discussed.During a 3-day period,UWC-3δ18O has been measured on Cameca IMS1280 Ion Microprobe Mass Spectrometer against"Oka"external standard.The measured mean value of UWC-3(δ18OVPDB=?17.85‰±0.22‰,1SD)matches well with its recommended value(δ18OVPDB=?17.83‰?0.08‰),suggesting that the instrument was stable.The same method applied on HS4 producedδ18O measurements at seasonal resolution with distinct annual cycles and the total cycle number in agreement with that from Mg/Ca cycles and lamination layer counting of the same section,so it offers an alternative for accessing speleothem time series.However,compared with conventionalδ18O values of HS4,SIMSδ18O values are more negative by 0.90‰with larger seasonal variation.The main reasons might come from the micro-cracks,micro-pores or liquid inclusions existing in HS4,and organic materials in the speleothem might be another factor affecting the SIMSδ18O values,indicating that to obtain reliable speleothem SIMSδ18O values,both compaction and purity of samples are crucial.  相似文献   

11.
Telogenetic epikarst carbon sourcing and transport processes and their associated hydrogeochemical responses are complex and dynamic. Carbon dioxide (CO2) transport rates in the epikarst zone are often driven by hydrogeochemical responses, which influence carbonate dissolution and conduit formation. This study examines the influence of land use on carbon sourcing and carbonate dissolution kinetics through a comparative analysis of separate, but similar, epikarst systems in south-central Kentucky. The use of high-resolution hydrogeochemical data from multiple data loggers and isotope analysis from collected water samples reflects the processes within these epikarst aquifers, which are estimated to contribute significantly to bedrock dissolution. Results indicate that, in an agricultural setting, long-term variability and dissolution is governed by seasonal production of CO2 . In a more urbanized, shallower epikarst system, land cover may affect CO2 transport between the soil and underlying bedrock. This concentration of CO2 potentially contributes to ongoing dissolution and conduit development, irrespective of seasonality. The observed responses in telogenetic epikarst systems seem to be more similar to eogenetic settings, which is suggested to be driven by CO2 transport occurring independent of high matrix porosity. The results of this study indicate site-specific responses with respect to both geochemical and δ13CDIC changes on a seasonal scale, despite regional geologic similarities. The results indicate that further comparative analyses between rural and urban landscapes in other karst settings is needed to delineate the impact of land use and seasonality on dissolution and carbon sourcing during karst formation processes. © 2019 John Wiley & Sons, Ltd.  相似文献   

12.
Sulfur contents and δ34S values of Somma-Vesuvius magmas are consistent with syneruptive, open-system degassing at temperatures of 800–850°C for Plinian pumices and 1100–1200°C for lavas. The extent of degassing appears to be greater in lavas than in pumices. The key parameter controlling the 34S/32S ratio of Somma-Vesuvius volcanics is the average magma oxidation state, which generally varies from 0.85 to 1.20 Δ NNO units for lavas and from 1.20 to 1.40 Δ NNO units for pumices. Consequently, S contents and δ34S values of magmas constitute a potentially valuable tool in estimating their average redox conditions. The results of this study may help in risk mitigation when the Vesuvius magmatic system evolves toward eruptive conditions. Received: 20 January 1998 / Accepted: 5 May 1998  相似文献   

13.
Aquatic plants are major input sources of autochthonous organic matter in lake sediments, but investigations on fatty acid(FA) and n-alkane distributions in aquatic plants are currently limited, greatly hindering the applications of their isotope geochemistry in lacustrine environments. Here, the reported n-alkyl lipid distributions of aquatic plants in globally studied lakes,together with newly obtained aquatic plant n-alkyl lipid data in Chinese lakes(Yunnan and Inner Mongolia), are used to understand their distribution characteristics. The results show that aquatic plants have predominantly mid-chain lipids(C_(23)–C_(25) n-alkanes and C_(22)–C_(24) FAs), differing from that of terrestrial plants(dominant by long-chain lipids), but the long-chain n-alkanes(e.g., C_(27) and C_(29)) and long-chain FAs(e.g., C_(26) and C_(28)) also show high abundances in most samples. Submerged plants have high concentrations of long-chain n-alkanes(avg. 47 μg g~(-1)) and long-chain FAs(avg. 170 μg g~(-1)), close to those in terrestrial plants, indicating that submerged plants may make large contributions of long-chain n-alkyl lipids to lake sediments, while the contributions of long-chain n-alkyl lipids derived from algae to lake sediments may be small because of their low concentrations(avg. 2 μg g~(-1) for n-alkanes and 9 μg g~(-1) for FAs). We find that lipid molecular proxies(including ACL_(14-32) and ATR_(14-18)) can be reliably used to distinguish the FAs sourced from algae and other plants, and Paq′ values can be utilized to distinguish the nalkane sources between submerged plants and terrestrial plants. Aquatic plants do not have significant δD differences among different chain-length n-alkanes and FAs for each sample, suggesting that the offset between δD values of different chain-length n-alkyl lipids in lake sediments can help determine sedimentary lipid input sources and infer paleohydrological changes.  相似文献   

14.
There have been a number of investigations for examining the possible link between long-term climate variability and solar activity.A continuous δ18O record of peat cellulose covering the past 6000 years and the response of climate variation inferred from the proxy record to solar forcing are reported.Results show that during the past 5000 years the abrupt climate variations,including 17 warming and 17 cooling,and a serious of periodicities,such as 86,101,110,127,132,140,155,207,245,311,820 and 1050 years,are strikingly correlative to the changes of solar irradiation and periodicity.These observations are considered as further evidence for a close relationship between solar activity and climate variations on time scales of decades to centuries.  相似文献   

15.
Stable isotopic signatures (δ13C and δ15N) and C/N ratios of suspended particulate organic matter (POM) were investigated from the surface water of Daya Bay during summer and winter of 2015. The relatively high δ13CPOM values suggested the input of 13C-depleted terrigenous organic matter was low in Daya Bay. There were significant correlations between δ13CPOM values and chlorophyll a concentrations both during summer and winter, suggesting the δ13CPOM values were mainly controlled by the phytoplankton biomass in the surface water. The distribution of δ15NPOM values was more complicated than that of δ13CPOM and displayed low values in the outer bay and the Dan'ao River estuary. 15N-depleted ammonia originating from industrial wastewater might have strongly influenced the water quality and stable isotopic signatures of POM near the Dan'ao River estuary. The δ13CPOM and δ15NPOM values strongly reflect the influences of anthropogenic activity and eutrophication in Daya Bay.  相似文献   

16.
Green macroalgae bioassays were used to determine if the δ15N signature of cruise ship waste water effluent (CSWWE) could be detected in a small harbor. Opportunistic green macroalgae (Ulva spp.) were collected, cultured under nutrient depleted conditions and characterized with regard to N content and δ15N. Samples of algae were used in controlled incubations to evaluate the direction of isotope shift from exposure to CSWWE. Algae samples exposed to CSWWE exhibited an increase of 1-2.5‰ in δ15N values indicating that the CSWWE had an enriched isotope signature. In contrast, algae samples exposed to field conditions exhibited a significant decrease in the observed δ15N indicating that a light N source was used. Isotopically light, riverine nitrogen derived from N2-fixing trees in the watershed may be a N source utilized by algae. These experiments indicate that the δ15N CSWWE signature was not detectable under the CSWWE loading conditions of this experiment.  相似文献   

17.
Oxygen stable isotope of atmospheric water vapor is widely used to study the modern process of cli- mate. Atmospheric water vapor samples were collected at Dlingha, northeast of Tibetan Plateau during the period from July 2005 to February 2006. The variation of δ18O and the relationships between δ18O and both the temperature and specific humidity are analyzed in this paper. Results show that the sea- sonal variation of δ18O of atmospheric water vapor at Delingha is remarkable with higher δ18O in summer and lower δ18O in winter. The temporal variation of vapor δ18O shows obvious fluctuations, with magnitude of over 37‰. The daily variation of the δ18O is highly correlated with air temperature. The relationship between δ18O and atmospheric water vapor content is complex. Study shows that δ18O of atmospheric water vapor is positively correlated with specific humidity in winter in seasonal scale and inversely correlated with specific humidity in summer rainy period. The δ18O values of at- mospheric water vapor are lower than those of precipitation at Delingha, and the average difference is 10.7‰. Variations of δ18O of atmospheric water vapor is also found to be affected by precipitation events, The model results show that the precipitation effect could have caused the vapor δ18O in the raining season to lower by 7% in average in July and August.  相似文献   

18.
 Oxygen-isotope analyses of lavas from Medicine Lake volcano (MLV), in the southern Cascade Range, indicate a significant change in δ18O in Holocene time. In the Pleistocene, basaltic lavas with <52% SiO2 averaged +5.9‰, intermediate lavas averaged +5.7‰, and silicic lavas (≥63.0% SiO2) averaged +5.6‰. No analyzed Pleistocene rhyolites or dacites have values greater than +6.3‰. In post-glacial time, basalts were similar at +5.7‰ to those erupted in the Pleistocene, but intermediate lavas average +6.8‰ and silicic lavas +7.4‰ with some values as high as +8.5‰. The results indicate a change in the magmatic system supplying the volcano. During the Pleistocene, silicic lavas resulted either from melting of low-18O crust or from fractionation combined with assimilation of very-low-18O crustal material such as hydrothermally altered rocks similar to those found in drill holes under the center of the volcano. By contrast, Holocene silicic lavas were produced by assimilation and/or wholesale melting of high-18O crustal material such as that represented by inclusions of granite in lavas on the upper flanks of MLV. This sudden shift in assimilant indicates a fundamental change in the magmatic system. Magmas are apparently ponding in the crust at a very different level than in Pleistocene time. Received: 6 March 1997 / Accepted: 12 January 1998  相似文献   

19.
Marble has a great potential to understand a history of various geological events occurring during tectonic processes. In order to decode metamorphic–metasomatic records on C–O isotope compositions of marble at mid-crustal conditions, we conducted a C–O–Sr isotope study on upper amphibolite-facies marbles and a carbonate–silicate rock from the Hida Belt, which was once a part of the crustal basement of the East Asian continental margin. Carbon and oxygen isotope analyses of calcite from marbles (Kamioka area) and a carbonate–silicate rock (Wadagawa area) show a large variation of δ13C [VPDB] and δ18O [VSMOW] values (from −4.4 to +4.2 ‰ and +1.6 to +20.8 ‰, respectively). The low δ13C values of calcites from the carbonate–silicate rock (from −4.4 to −2.9 ‰) can be explained by decarbonation (CO2 releasing) reactions; carbon–oxygen isotope modeling suggests that a decrease of δ13C strongly depends on the amount of silicate reacting with carbonates. The occurrence of metamorphic clinopyroxene in marbles indicates that all samples have been affected by decarbonation reactions. All δ18O values of calcites are remarkably lower than the marine-carbonate values. The large δ18O variation can be explained by the isotope exchange via interactions between marble, external fluids, and/or silicates. Remarkably low δ18O values of marbles that are lower than mantle value (~+5 ‰) suggest the interaction with meteoric water at a later stage. Sr isotope ratios (87Sr/86Sr = 0.707255–0.708220) might be close to their protolith values. One zircon associated with wollastonite in a marble thin-section yields a U–Pb age of 222 ± 3 Ma, which represents the timing of the recrystallization of marble, triggered by H2O-rich fluid infiltration at a relatively high-temperature condition. Our isotope study implies that the upper amphibolite-facies condition, like the Hida Belt, might be appropriate to cause decarbonation reactions which can modify original isotope compositions of marble if carbonates react with silicates.  相似文献   

20.
The sorption of AuCl4 −,AuCl2 − and Au(S2O3)3- on δ-MnO2 was investigated at pH2–11.6, 0.01 mol/L and 0.1 mol/L NaNO3 solutions. At pH 4 in two electrolyte strength solutions, Au sorption densities on δ-MnO2 are 0.18–0.21 and 0.28μmoL/m2 for AuCl4 − and Au(S2O3)2 3-, respectively, and the Au surface coverage is approximate to or lower than 1%. This adsorption of the two Au complexes decreases as the solution pH increases, which conforms to the sorption regularity of the anion on δ-MnO2. The Au sorption decreases in the sequence of Au(S2O3)2 3- >AuCl4 − >AuC12 −. The intrinsic equilibrium constants (logK int) of the three Au complexes are 1.17–2.7, much higher than those of Cu and Cd. The hydrolysis products of AuCl4 - are preferentially adsorbed by δ-MnO2 and the inner-sphere Au-surface complexes are formed on the surface. Project supported by the National Studying-abroad Foundation, the National Natural Science Foundation of China (Grant No. 49573200) and the Australian Mining Industry.  相似文献   

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