New insights into diffusive kinetic fractionation during liquid condensation under supersaturated environment: an alternative approach for isotope tagging of ground-level water vapour.

Stable water isotopes in ground-level vapour are key to estimating water exchange between geospheres. Their sampling, however, is limited to laser-absorption spectrometers and satellite observations, having inherent shortcomings. This study investigates diffusive kinetic fractionation during liquid condensation under supersaturated environment, providing a cost-effective, reliable way of sampling ground-level vapour isotopes (18O, 2H). Experiments were undertaken at three locations in India with 'liquid' samples collected from condensation of ambient air at 0°C. Simultaneously, pristine 'vapour' was sampled via cryogenic-trapping using liquid nitrogen-alcohol slush at -78°C. The 'liquid' condensed under supersaturation was progressively more depleted in 18O, and less enriched in 2H than expected under equilibrium fractionation, with an increasing degree of supersaturation expressed as saturation index (Si). This study revealed: (1) Si, molecular density, Rh, T together control the extent of isotopic kinetic fractionation. (2) The presence of diffusive concentration gradient inhibits the flow of heavier isotopes during liquid condensation. (3) The stochastic nature of the process cannot be explained using a physics-based model alone. The artificial neural network model is hence deployed to sample δ18O (δ 2H) within -0.24 ± 1.79‰ (0.53 ± 11.23 ‰) of true value. (4) The approach can be extended to ground-validate isotope-enabled general circulation models and satellite observations.

In vitro application of carbonic anhydrase to accelerate the equilibration of 18O between H2O and CO2 for the rapid measurement of 18O/16O isotope ratios in aqueous samples.

A novel method of the accelerated equilibration of 18O between CO2 and H2O for the measurement of the 18O/16O isotope ratios in aqueous samples with natural isotope abundances is presented. This rapid equilibrium method is based on the in vitro application of the enzyme carbonic anhydrase (CA). The CA from bovine erythrocytes was adsorptively fixed to 3-mm glass beads with an etched surface. After the addition of this carrier-fixed CA catalyst to the water sample, the isotope equilibrium was already reached after 1 h. The previously used non-catalysed 18O isotope exchange in water samples needs about 24 h. Whole blood samples also showed fast 18O isotope equilibration, which definitely results from the native presence of CA in erythrocytes. By shortening the time for sample preparation, the CA catalysed technique can significantly increase the throughput of the samples to be measured, and also 18O and 2H measurement by means of isotope ratio mass spectrometry (IRMS) may be synchronized. The 2H and 18O sample preparation can be performed in the same reaction vessel because cross-effects at the simultaneous use of Pt and CA catalysts do not occur.

Sources and transport of selected organic micropollutants in urban groundwater underlying the city of Halle (Saale), Germany.

In this study, we used isotopic (delta18O, delta2H, delta34S-SO4) and chemical tracers (boron) to assess the sources and transport processes of the micropollutants carbamazepine, galaxolide, and bisphenol A in groundwater underlying the city of Halle (Saale), Germany. Their ubiquitous presence in urban groundwater results from a combination of local river water infiltration, sewer exfiltration, and urban stormwater recharge. Attenuation during transport with infiltrating river water increased from carbamazepine (0-60%) to galaxolide (60-80%) in accordance with their increasing sorption affinity and decreasing recalcitrance against biodegradation. Distinctly higher attenuation during transport was found for carbamazepine (85-100%) and galaxolide (95-100%) if micropollutants originated from sewer exfiltration. Most likely, this is related to higher contents of organic matter and higher transit times of the respective flow paths. Although attenuation undoubtedly also affects the transport of bisphenol A, quantification is limited due to additional contributions from the urban stormwater recharge. As a consequence, micropollutant loads in groundwater indicate that groundwater discharge may dominate the export of bisphenol A from urban areas.

Nitrate degradation without 15N enrichment: a hydrochemical and isotopic study of a fractured rock aquifer including embedded lakes.

Water samples from three quarry lakes and the surrounding fractured rock aquifer were investigated for delta18O and delta2H (H2O), delta15N and delta18O (NO3-), as well as anions and cations. Lake water and groundwater can be distinguished by their different chemical and isotopic composition. Because of evaporation processes, 18O and 2H are enriched in the lake water and can be used as natural tracers for the water dynamic of the lakes. The groundwater is characterised by high nitrate concentrations (up to 120 mg/l). Lake internal processes reduce the nitrate concentration in the quarry lakes. However, no enrichment of delta15N and delta18O in nitrate, typical for microbial nitrate degradation, is observed in the lake water. Because of the complex flow paths in the fractured rock aquifer and the intense chemical transformations at the interface between groundwater and lake water, isotopic and hydrochemical data of lake water and groundwater alone do not conclusively explain hydrological and hydrochemical processes of the investigated lake-groundwater system.

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.

Contributions of the different water sources to the Elqui river runoff (northern Chile) evaluated by H/O isotopes.

We present the results of an isotope (2H and 18O) and hydrogeochemical study in order to constrain the origin, recharge, and evolution of the surface and groundwater in the arid Andean realm of the Elqui watershed. The results of 2H and18O analyses of water samples obtained during our summer and winter campaigns indicate a generally meteoric origin of the river and spring waters of the watershed. The isotope signature of water of the Elqui river and its tributaries as well as that of groundwater in the coastal region fits the 2H-18O relation of delta2H =7.61delta18O+6.1. A relatively fast discharge and a quasi-closed catchment area can be asserted for water along the river flow path. The tributaries from the more arid coastal area, north of the Elqui river, differ in their isotopic signature due to evaporation and hydrochemically due to interactions with the strongly altered and fractured volcanic rocks of the basement. In the Andean zone, the18O-enriched hydrothermal spring of Baños del Toro exhibits the influence of water-rock interaction processes. The chemistry of the river water changes from sulphate- to chloride-rich along the river course from the high Andean mountains to the coast. The sulphate-rich character of these Andean waters reflects their passage through sulphide-rich rock massifs that were subjected to strong oxidation processes in the near superficial environment. This sulphate signature is enforced by past and present mining of precious metal epithermal deposits (e.g. those of El Indio-Tambo Au-Cu-As district), in which mineralised zones were developed during a series of Miocene magmatic-hydrothermal episodes in the Andean realm. Owing to the proximity of the lower Elqui river waters and its tributaries to the Pacific coast, the chloride character may be induced by agricultural and marine (sea spray, fog) sources. Generally, the main source of the Elqui river water is mainly attributed to surface runoff and less to contributions from the basement fractured aquifer.

Microbial nitrogen transformation in constructed wetlands treating contaminated groundwater.

Pathways of ammonium (NH4 (+)) removal were investigated using the stable isotope approach in constructed wetlands (CWs). We investigated and compared several types of CWs: planted horizontal subsurface flow (HSSF), unplanted HSSF, and floating plant root mat (FPRM), including spatial and seasonal variations. Plant presence was the key factor influencing efficiency of NH4 (+) removal in all CWs, what was illustrated by lower NH4 (+)-N removal by the unplanted HSSF CW in comparison with planted CWs. No statistically significant differences in NH4 (+) removal efficiencies between seasons were detected. Even though plant uptake accounted for 32-100 % of NH4 (+) removal during spring and summer in planted CWs, throughout the year, most of NH4 (+) was removed via simultaneous nitrification-denitrification, what was clearly shown by linear increase of δ(15)N-NH4 (+) with decrease of loads along the flow path and absence of nitrate (NO3 (-)) accumulation. Average yearly enrichment factor for nitrification was -7.9 ‰ for planted HSSF CW and -5.8 ‰ for FPRM. Lack of enrichment for δ(15)N-NO3 (-) implied that other processes, such as nitrification and mineralization were superimposed on denitrification and makes the stable isotope approach unsuitable for the estimation of denitrification in the systems obtaining NH4 (+) rich inflow water.

Stable H and O isotope variations reveal sources of recharge in Dhofar, Sultanate of Oman.

Due to the ability of stable water isotopes to characterize the origin of water and connected processes of groundwater recharge, we used the isotope variations of hydrogen and oxygen in different water sources for assessing the recharge process in the Dhofar region. δ(18)O and δ(2)H of precipitation, spring water, and groundwater cover a range from -10 to +2 and from -70 to +7 ‰ (vs Vienna Standard Mean Ocean Water), respectively, and correlate in a linear relationship close to the Global Meteoric Water Line. No obvious evaporation processes are detected. A clear signal of the recent precipitation is given by the annual monsoon. The monsoon signal is confirmed by several springs existing in the south at the foot of the Dhofar mountains and sources at Gogub above 450 m and Tawi Atir at 650 m above sea level. They occur here first in the form of water intercepted by trees as stemflow and throughflow. The isotope signature of groundwater in the Dhofar mountains reflects the climatic conditions at the time of recharge and the lithological features of the limestone matrix. To the north, the isotope patterns of the groundwater are continuously depleted from the monsoon signal along the outcropping aquifer D (Lower Umm Er Radhuma). Here, a more negative signature towards the wells in the Najd desert region was observed. Cyclone water that flooded wadis in the Dhofar region occasionally, as observed in November 2011, falls isotopically into the same range as we observed in the fossil groundwater. Taking into account the different sources of precipitation and groundwater and thus a clear distinction of the isotopic composition of the water sources, we conclude a recharge process divided into a southward and a northward component in the Dhofar region.

Isotope variations of hydrogen, carbon and nitrogen in florae from the Schirmacher Oasis, East Antarctica.

Comparative biochemical and isotope-chemical investigations of cosmopolitical plants open up ways of obtaining parameters from different parts of the Earth which are characterised by variations in the habitat due to different environments. As an Antarctic oasis, the Schirmacher Oasis disposes of adequate favourable ecological conditions for the growth of lower plants. In the present paper, results of isotope studies of lichens, mosses and algae of the Schirmacher Oasis are given and peculiarities of the habitats which influence the isotope contents of the plants are discussed.

Micropollutant loads in the urban water cycle.

The assessment of micropollutants in the urban aquatic environment is a challenging task since both the water balance and the contaminant concentrations are characterized by a pronounced variability in time and space. In this study the water balance of a central European urban drainage catchment is quantified for a period of one year. On the basis of a concentration monitoring of several micropollutants, a contaminant mass balance for the study area's wastewater, surface water, and groundwater is derived. The release of micropollutants from the catchment was mainly driven by the discharge of the wastewater treatment plant. However, combined sewer overflows (CSO) released significant loads of caffeine, bisphenol A, and technical 4-nonylphenol. Since an estimated fraction of 9.9-13.0% of the wastewater's dry weather flow was lost as sewer leakages to the groundwater, considerable loads of bisphenol A and technical 4-nonylphenol were also released by the groundwater pathway. The different temporal dynamics of release loads by CSO as an intermittent source and groundwater as well as treated wastewater as continuous pathways may induce acute as well as chronic effects on the receiving aquatic ecosystem. This study points out the importance of the pollution pathway CSO and groundwater for the contamination assessments of urban water resources.

Temporal and spatial patterns of micropollutants in urban receiving waters.

Based on a monitoring program over the course of a year, we characterize the temporal and spatial distribution of selected micropollutants in an urban watershed within the city of Leipzig, Germany. Micropollutants revealed a ubiquitous presence in untreated and treated wastewater, surface water and groundwater. The loads of 4-nonylphenol in the effluents of the municipal wastewater treatment plant followed a seasonal trend, whereas the loads of all other micropollutants were highly variable and not correlated to seasons. In the surface water, load seasonality of caffeine, galaxolide and tonalide resulted from a rapid removal with increased water temperature. The loads of 4-nonylphenol and of caffeine in the colder months increased when rainfall occurred. In the groundwater, complex spatial and temporal patterns were apparent and were related to varying input, retardation and removal processes. As a consequence, an assessment of micropollutants in urban waters should consider different micropollutants' temporal and spatial variability.