Sulphur and oxygen isotopic characters of dissolved sulphate in groundwater from the Pleistocene aquifer in the southern Jordan Valley (Jericho area, Palestine)

Sulphate and chloride concentrations in the shallow Pleistocene aquifer systems in the lower Jordan valley area indicate a general trend of increasing salinity eastward and southward. This study was conducted in one of the important sub-basins feeding the Pleo-Pleistocene aquifer in the Jericho area in the southern part of the valley using S and O isotopes of dissolved sulphate. The results show that sulphate has mainly two contributions to the groundwater. One is the surface seepage, which is present as a salty leachate form with the positive delta34Ssulphate values of primary gypsum in Lisan and Samara formations, and the second is the upwelling saline water which was in contact with a deep secondary gypsum, aragonites and salty rocks and rose up under heavy abstraction with depleted 34S in sulphate and relatively high sulphate and chloride content. The latest was clearly shown in the Arab Project wells to the east that is undergoing a continuous heavy abstraction. The isotopic signatures of S and O in these wells to the east show that this depleted 34S and highly concentrated sulphate might also indicate a dissolved sulphate originating from pyrite oxidation that results from the interaction with a pyrite-rich aquifer, which can well up with salty water under heavy abstraction and is oxidised in the upper aerobic shallow aquifer.     

Hydrogeochemical and isotopic characterisation of groundwater in a sand-dune phreatic aquifer on the northeastern coast of the province of Buenos Aires,Argentina

This contribution presents the hydrochemical and isotopic characterisation of the phreatic aquifer located in the Partido de la Costa, province of Buenos Aires, Argentina. In the sand-dune barrier geomorphological environment, groundwater is mainly a low-salinity Ca-HCO₃ and Na-HCO₃-type, being in general suitable for drinking, whereas in the continental plain (silty clay sediments), groundwater is a Na-Cl type with high salinity and unsuitable for human consumption. The general isotopic composition of the area ranges from?6.8 to?4.3 ‰ for δ¹⁸O and from?39 to?21 ‰ for δ²H, showing that rainwater rapidly infiltrates into the sandy substrate and reaches the water table almost without significant modification in its isotopic composition. These analyses, combined with other chemical parameters, made it possible to corroborate that in the eastern area of the phreatic aquifer, there is no contamination from marine salt water.     

Sources and circulation of water and arsenic in the Giant Mine,Yellowknife, NWT,Canada

Recovery of gold from arsenopyrite-hosted ore in the Giant Mine camp, Yellowknife, NWT, Canada, has left a legacy of arsenic contamination that poses challenges for mine closure planning. Seepage from underground chambers storing some 237,000 tonnes of arsenic trioxide dust, has As concentrations exceeding 4000 ppm. Other potential sources and sinks of As also exist. Sources and movement of water and arsenic are traced using the isotopes of water and sulphate. Mine waters (16 ppm As; As^V/As^III ≈ 150) are a mixture of two principal water sources – locally recharged, low As groundwaters (0.5 ppm As) and Great Slave Lake (GSL; 0.004 ppm As) water, formerly used in ore processing and discharged to the northwest tailings impoundment (NWTP). Mass balance with δ¹⁸O shows that recirculation of NWTP water to the underground through faults and unsealed drillholes contributes about 60% of the mine water. ;[emsp]>Sulphate serves to trace direct infiltration to the As₂O₃ chambers. Sulphate in local, low As groundwaters (0.3–0.6 ppm As; δ³⁴S_SO4  ～ 4 ‰ and δ¹⁸O_SO4  ～ ? 10 ‰) originates from low-temperature aqueous oxidation of sulphide-rich waste rock. The high As waters gain a component of ¹⁸O-enriched sulphate derived from roaster gases (δ¹⁸O_SO4  = + 3.5 ‰), consistent with their arsenic source from the As₂O₃ chambers. High arsenic in NWTP water (～ 8 ppm As; δ¹⁸O_SO4  = ? 2 ‰) derived from mine water, is attenuated to close to 1 ppm during infiltration back to the underground, probably by oxidation and sorption by ferrihydrite.     

Regional and temporal variability of the isotope composition (O, S) of atmospheric sulphate in the region of Freiberg, Germany, and consequences for dissolved sulphate in groundwater and river water

The isotope composition of dissolved sulphate and strontium in atmospheric deposition, groundwater, mine water and river water in the region of Freiberg was investigated to better understand the fate of these components in the regional and global water cycle. Most of the isotope variations of dissolved sulphates in atmospheric deposition from three locations sampled bi- or tri-monthly can be explained by fractionation processes leading to lower [Formula: see text] (of about 2-3‰) and higher [Formula: see text] (of about 8-10‰) values in summer compared with the winter period. These samples showed a negative correlation between [Formula: see text] and [Formula: see text] values and a weak positive correlation between [Formula: see text] and [Formula: see text] values. They reflect the sulphate formed by aqueous oxidation from long-range transport in clouds. However, these isotope variations were superimposed by changes of the dominating atmospheric sulphate source. At two of the sampling points, large variations of mean annual [Formula: see text] values from atmospheric bulk deposition were recorded. From 2008 to 2009, the mean annual [Formula: see text] value increased by about 5‰; and decreased by about 4‰ from 2009 to 2010. A change in the dominating sulphate source or oxidation pathways of SO(2) in the atmosphere is proposed to cause these shifts. No changes were found in corresponding [Formula: see text] values. Groundwater, river water and some mine waters (where groundwater was the dominating sulphate source) also showed temporal shifts in their [Formula: see text] values corresponding to those of bulk atmospheric deposition, albeit to a lower degree. The mean transit time of atmospheric sulphur through the soil into the groundwater and river water was less than a year and therefore much shorter than previously suggested. Mining activities of about 800 years in the Freiberg region may have led to large subsurface areas with an enhanced groundwater flow along fractures and mined-refilled ore lodes which may shorten transit times of sulphate from precipitation through groundwater into river water.     

Stable isotopic and geochemical variability within shallow groundwater beneath a hardwood hammock and surface water in an adjoining slough (Everglades National Park,Florida, USA)

Data from a 10-month monitoring study during 2007 in the Everglades ecosystem provide insight into the variation of δ¹⁸O, δD, and ion chemistry in surface water and shallow groundwater. Surface waters are sensitive to dilution from rainfall and input from external sources. Shallow groundwater, on the other hand, remains geochemically stable during the year. Surface water input from canals derived from draining agricultural areas to the north and east of the Everglades is evident in the ion data. δ¹⁸O and δD values in shallow groundwater remain near the mean of?2.4 and?12 ‰, respectively. ¹⁸O and D values are enriched in surface water compared with shallow groundwater and fluctuate in sync with those measured in rainfall. The local meteoric water line (LMWL) for precipitation is in close agreement with the global meteoric water line; however, the local evaporation line (LEL) for surface water and shallow groundwater is δ D=5.6 δ¹⁸O+1.5, a sign that these waters have experienced evaporation. The intercept of the LMWL and LEL indicates that the primary recharge to the Everglades is tropical cyclones or fronts. δ deuterium to δ¹⁸O excess (D_ex values) generally reveal two moisture sources for precipitation, a maritime source during the fall and winter (D _ex>10 ‰) and a continental-influenced source (D _ex<10 ‰) in the spring and summer.     

Statistical properties of turbidity, oxygen and pH fluctuations in the Seine river estuary (France)

We consider here, the fluctuations of turbidity, oxygen and pH time series recorded from the MAREL system (Ifremer, France), which is based on the deployment of data buoys equipped with water analysis capabilities in an automated mode. We perform a spectral analysis (from 10 min to years) of these time series, and we estimate their probability density functions. Oxygen, turbidity and pH are important quantities for ecosystem studies and physics-biology couplings, and their fluctuations reveal the possible influence of environmental factors such as tides and turbulence. Turbidity variability is highly complex and does not appear to be directly coupled to turbulence, since no clear range is visible. On the other hand, oxygen percentage of saturation and pH data show remarkably nice scaling ranges, indicating an important coupling with turbulence, but also biological or chemical activity, since the statistics differ markedly from passive scalars. Several possible sources of this variability are discussed.     

Influence of the balance of the intertropical front on seasonal variations of the isotopic composition in rainfall at Kisiba Masoko (Rungwe Volcanic Province,SW, Tanzania)

Tropical rainfall isotopic composition results from complex processes. The climatological and environmental variability in East Africa increases this complexity. Long rainfall isotope datasets are needed to fill the lack of observations in this region. At Kisiba Masoko, Tanzania, rainfall and rain isotopic composition have been monitored during 6 years. Mean year profiles allow to analyse the seasonal variations. The mean annual rainfall is 2099?mm with a rain-weighted mean composition of ?3.2?‰ for δ¹⁸O and ?11.7?‰ for δ²H. The results are consistent with available data although they present their own specificity. Thus, if the local meteoric water line is δ²H?=?8.6 δ¹⁸O?+?14.8, two seasonal lines are observed. The seasonality of the isotopic composition in rain and deuterium excess has been compared with precipitating air masses backtracking trajectories to characterize a simple scheme of vapour histories. The three major oceanic sources have two moisture signatures with their own trajectory histories: one originated from the tropical Indian Ocean at the beginning of the rainy season and one from the Austral Ocean at its end. The presented isotopic seasonality depends on the balance of the intertropical front and provides a useful dataset to improve the knowledge about local processes.     

Insights from stable isotopes of water and hydrochemistry to the evolutionary processes of groundwater in the Subei lake basin,Ordos energy base,Northwestern China

ABSTRACT

Changes in groundwater evolutionary processes due to aquifer overexploitation show a world-wide increase and have been of growing concern in recent years. The study aimed to improve the knowledge of groundwater evolutionary processes by means of stable water isotopes and hydrochemistry in a representative lake basin, Ordos energy base. Groundwater, precipitation, and lake water collected during four campaigns were analysed by stable isotopes and chemical compositions. Results showed that temperature effect predominated the isotope fractionation in precipitation, while evaporation and inadequate groundwater recharge were the key factors explaining high salinity and isotopic enrichment in lake water. Additionally, the Kuisheng Lake was a preferential area of groundwater recharge, while the Subei Lake received less sources from underlying aquifer due to the combined effects of low permeable zone and upstream groundwater captured by the production wells. The homogeneous isotope signatures of groundwater may be ascribed to the closely vertical hydraulic connectivity between the unconfined and the confined aquifers. Isotopically enriched groundwater pumping from well field probably promoted isotopic depletion in groundwater depression cone. These findings not only provide the conceptual framework for the inland basin, but also have important implications for sustainable groundwater management in other groundwater discharge basins with arid climate.     

洱海水-陆界面溶解性有机氮组成结构及生物有效性-以永安江为例

利用紫外与三维荧光光谱技术,研究了洱海水-陆界面溶解性有机氮(DON)组成结构及生物有效性特征,并探讨了其对湖泊水质影响。结果表明：(1)水-陆界面经由永安江输入洱海DON浓度在0.25～1.39 mg·L-1之间,从河流到湖内以夏秋两季DON浓度较高;经由永安江输入洱海DON负荷量在0.48～2.34 t之间,其中以夏季DON负荷量最高,表明经由入湖河流输入洱海的DON对洱海水质影响潜在风险较大,尤其夏季明显。(2)水-陆界面经由永安江输入洱海的DON组成主要以类腐殖质物质为主,永安江沿程到湖内衰解特征明显且生物有效性为15.27%,而类蛋白和可溶性微生物代谢产物则出现不同程度累积,累积率分别为42.00%和20.68%;DON组分的分子腐殖化程度经由永安江到洱海湖内呈渐降趋势且降低了14.97%。同时,分子芳香环取代基从以脂肪链为主逐渐向以羰基、羧基、羟基、酯类为主转变,尤其在夏季表现明显。(3)水-陆界面经由永安江输入洱海DON组成特征参数(P_{(Ⅲ+Ⅴ, n)}/P_{(Ⅰ+Ⅱ, n)}和A₂₅₃/A₂₀₃值)与其不同形态氮含量显著相关(R2=0.64～0.74, P<0.1,P<0.05),即永安江输入洱海DON结构影响其生物有效性;水-陆界面DON不同结构特征参数与水质呈显著正相关(R=0.82～0.96, p<0.05,p<0.01),表明水-陆界面经由永安江入湖DON组成结构及生物有效性对洱海水污染有一定贡献,尤其在夏季受陆源等人类活动影响较大时,影响更为突出;由此可见,洱海水-陆界面经由永安江入湖DON组成结构变化(如P_{(Ⅲ+Ⅴ, n)}/P_{(Ⅰ+Ⅱ, n)},A₂₅₃/A₂₀₃)可在一定程度上反映洱海水质状况。