Reproducibility and accuracy of noble gas measurements on water samples in the microlitre range.

RATIONALE: In order to derive meaningful noble gas temperatures (NGTs) from speleothem fluid inclusions, precise and accurate measurements of noble gas concentrations on very small water samples are necessary. To optimise these measurements and their reliability, an investigation of the reproducibility and accuracy of the analytical procedure is essential. METHODS: Water equilibrated with air under controlled conditions was filled into copper capillaries to produce small (about 1 µL) air-equilibrated water samples (so-called µAEWs). As speleothem samples, the µAEWs were opened in a crusher and the released noble gases analysed with an electron ionisation sector field mass spectrometer run in static mode. For better comparability with speleothem samples, a defined amount of air was added to the noble gases derived from one group of µAEWs. RESULTS: The reproducibility of the experimental procedure was found to be better than 2.2% for all relevant noble gases. Within these uncertainties, the measured noble gas concentrations of µAEWs agree with expectations. The corresponding NGTs reproduce within 0.5°C and deviate by less than 1°C from the equilibration temperature. In the case of air addition, the air to water ratio was determined accurately and, excluding one outlier, the NGTs were determined with a reproducibility and accuracy well below 1°C. CONCLUSIONS: The results show that the used measurement procedure is generally suitable to reveal major climatic temperature changes, for which an overall NGT error of less than 1°C is desirable, from very small water samples as obtained from speleothem fluid inclusions.

Assessing the use of 3H-3He dating to determine the subsurface transit time of cave drip waters.

(3)H-(3)He measurements constitute a well-established method for the determination of the residence time of young groundwater. However, this method has rarely been applied to karstified aquifers and in particular to drip water in caves, despite the importance of the information which may be obtained. Besides the determination of transfer times of climate signals from the atmosphere through the epikarst to speleothems as climate archives, (3)H-(3)He together with Ne, Ar, Kr, Xe data may also help to give new insights into the local hydrogeology, e.g. the possible existence of a perched aquifer above a cave. In order to check the applicability of (3)H-(3)He dating to cave drips, we collected drip water samples from three adjacent caves in northwestern Germany during several campaigns. The noble gas data were evaluated by inverse modelling to obtain recharge temperature and excess air, supporting the calculation of the tritiogenic (3)He and hence the (3)H-(3)He age. Although atmospheric noble gases were often found to be close to equilibrium with the cave atmosphere, several drip water samples yielded an elevated (3)He/(4)He ratio, providing evidence for the accumulation of (3)He from the decay of (3)H. No significant contribution of radiogenic (4)He was found, corresponding to the low residence times mostly in the range of one to three years. Despite complications during sampling, conditions of a perched aquifer could be confirmed by replicate samples at one drip site. Here, the excess air indicator ΔNe was about 10 %, comparable to typical values found in aquifers in mid-latitudes. The mean (3)H-(3)He age of 2.1 years at this site presumably refers to the residence time in the perched aquifer and is lower than the entire transit time of 3.4 years estimated from the tritium data.

Dating of 'young' groundwaters using environmental tracers: advantages, applications, and research needs.

Many problems related to groundwater supply and quality, as well as groundwater-dependent ecosystems require some understanding of the timescales of flow and transport. For example, increased concern about the vulnerabilities of 'young' groundwaters (less than ~1000 years) to overexploitation, contamination, and land use/climate change effects are driving the need to understand flow and transport processes that occur over decadal, annual, or shorter timescales. Over the last few decades, a powerful suite of environmental tracers has emerged that can be used to interrogate a wide variety of young groundwater systems and provide information about groundwater ages/residence times appropriate to the timescales over which these systems respond. These tracer methods have distinct advantages over traditional approaches providing information about groundwater systems that would likely not be obtainable otherwise. The objective of this paper is to discuss how environmental tracers are used to characterise young groundwater systems so that more researchers, water managers, and policy-makers are aware of the value of environmental tracer approaches and can apply them in appropriate ways. We also discuss areas where additional research is required to improve ease of use and extend quantitative interpretations of tracer results.

Accumulation of natural SF6 in the sedimentary aquifers of the North China Plain as a restriction on groundwater dating.

We employed environmental tracers ((3)H-(3)He, SF(6)) in a study investigating the groundwater recharge in the North China Plain (NCP), a sedimentary aquifer system consisting of fluvial and alluvial river deposits near the city of Shijiazhuang. The (3)H-(3)He dating method revealed reasonable results for the young groundwater with ages covering the range of recent to ~40 a. SF(6) samples were taken in parallel for independent dating and to compare the applicability of both methods. However, the SF(6)-results are influenced and, in part, dominated by a systematic non-atmospheric component, revealing that the dating with SF(6) is unreliable in this region. A correlation of non-atmospheric SF(6) and (3)H-(3)He ages suggests a continuous accumulation of natural SF(6) in the groundwater of the NCP aquifers. Although terrigenic SF(6) has previously been associated with crystalline or igneous rocks, our results indicate that it can also be accumulated in sandy aquifers on the timescale relevant for SF(6) dating.

Trace elements in recent groundwater of an artesian flow system and comparison with snow: enrichments, depletions, and chemical evolution of the water.

Snow samples collected from hand-dug pits at two sites in Simcoe County, Ontario, Canada were analysed for major and trace elements using the clean lab methods established for polar ice. Potentially toxic, chalcophile elements are highly enriched in snow, relative to their natural abundance in crustal rocks, with enrichment factor (EF) values (calculated using Sc) in the range 107 to 1081 for Ag, As, Bi, Cd, Cu, Mo, Pb, Sb, Te, and Zn. Relative to M/Sc ratios in snow, water samples collected at two artesian flows in this area are significantly depleted in Ag, Al, Be, Bi, Cd, Cr, Cu, Ni, Pb, Sb, Tl, V, and Zn at both sites, and in Co, Th and Tl at one of the sites. The removal from the waters of these elements is presumably due to such processes as physical retention (filtration) of metal-bearing atmospheric aerosols by organic and mineral soil components as well as adsorption and surface complexation of ionic species onto organic, metal oxyhydroxide and clay mineral surfaces. In the case of Pb, the removal processes are so effective that apparently "natural" ratios of Pb to Sc are found in the groundwaters. Tritium measurements show that the groundwater at one of the sites is modern (ie not more than 30 years old) meaning that the inputs of Pb and other trace elements to the groundwaters may originally have been much higher than they are today; the M/Sc ratios measured in the groundwaters today, therefore, represent a conservative estimate of the extent of metal removal along the flow path.Lithogenic elements significantly enriched in the groundwaters at both sites include Ba, Ca, Li, Mg, Mn, Na, Rb, S, Si, Sr, and Ti. The abundance of these elements can largely be explained in terms of weathering of the dominant silicate (plagioclase, potassium feldspar, amphibole and biotite) and carbonate minerals (calcite, dolomite and ankerite) in the soils and sediments of the watershed. Arsenic, Mo, Te, and especially U are also highly enriched in the groundwaters, due to chemical weathering: these could easily be explained if there are small amounts of sulfides (As, Mo, Te) and apatite (U) in the soils of the source area. Elements neither significantly enriched nor depleted at both sites include Fe, Ga, Ge, and P.