22 research outputs found

    Groundwater ages, recharge conditions and hydrochemical evolution of a barrier island freshwater lens (Spiekeroog, Northern Germany)

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    Freshwater lenses below barrier islands are dynamic systems affected by changes in morphodynamic patterns, groundwater recharge and discharge. They are also vulnerable to pollution and overabstraction of groundwater. Basic knowledge on hydrogeological and hydrochemical processes of freshwater lenses is important to ensure a sustainable water management, especially when taking into account possible effects of climate change. This is the first study which gives a compact overview on the age distribution, recharge conditions and hydrochemical evolution of a barrier island freshwater lens in the southern North Sea (Spiekeroog Island, Eastfrisian Wadden Sea). Two ground- and surface water sampling campaigns were carried out in May and July 2011, supplemented by monthly precipitation sampling from July to October. 3H–3He ages, stable oxygen and hydrogen isotopes and major ion concentrations show that the freshwater lens reaches a depth of 44 mbsl, where an aquitard constrains further expansion in vertical direction. Groundwater ages are increasing from 4.4 years in 12 mbsl up to >70 years at the freshwater– saltwater interface. Stable isotope signatures reflect average local precipitation signatures. An annual recharge rate of 300–400 mm was calculated with 3H–3He data. Freshwater is primarily of Na–Ca–Mg–HCO3– and Ca–Na–HCO3–Cl type, while lowly mineralized precipitation and saltwater are of Na–Cl types. A trend towards heavier stable isotope signatures and higher electric conductivities in the shallower, younger groundwater within the freshwater lens may indicate increasing atmospheric temperatures in the last 30 years

    Modulation of Cosmogenic Tritium in Meteoric Precipitation by the 11-year Cycle of Solar Magnetic Field Activity

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    The relationship between the atmospheric concentration of cosmogenic isotopes, the change of solar activity and hence secondary neutron flux has already been proven. The temporal atmospheric variation of the most studied cosmogenic isotopes shows a significant anti-correlation with solar cycles. However, since artificial tritium input to the atmosphere due to nuclear-weapon tests masked the expected variations of tritium production rate by three orders of magnitude, the natural variation of tritium in meteoric precipitation has not previously been detected. For the first time, we provide clear evidence of the positive correlation between the tritium concentration of meteoric precipitation and neutron flux modulated by solar magnetic activity. We found trends in tritium time series for numerous locations worldwide which are similar to the variation of secondary neutron flux and sun spot numbers. This variability appears to have similar periodicities to that of solar cycle. Frequency analysis, cross correlation analysis, continuous and cross wavelet analysis provide mathematical evidence that the correlation between solar cycle and meteoric tritium does exist. Our results demonstrate that the response of tritium variation in precipitation to the solar cycle can be used to help us understand its role in the water cycle

    Groundwater age distributions at a public drinking water supply well field derived from multiple age tracers (⁸⁵Kr, ³H/³He, and ³⁹Ar)

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    Groundwater age is a key aspect of production well vulnerability. Public drinking water supply wells typically have long screens and are expected to produce a mixture of groundwater ages. The groundwater age distributions of seven production wells of the Holten well field (Netherlands) were estimated from tritium-helium (3H/3He), krypton-85 (85Kr), and argon-39 (39Ar), using a new application of a discrete age distribution model and existing mathematical models, by minimizing the uncertainty-weighted squared differences of modeled and measured tracer concentrations. The observed tracer concentrations fitted well to a 4-bin discrete age distribution model or a dispersion model with a fraction of old groundwater. Our results show that more than 75 of the water pumped by four shallow production wells has a groundwater age of less than 20 years and these wells are very vulnerable to recent surface contamination. More than 50 of the water pumped by three deep production wells is older than 60 years. 3H/3He samples from short screened monitoring wells surrounding the well field constrained the age stratification in the aquifer. The discrepancy between the age stratification with depth and the groundwater age distribution of the production wells showed that the well field preferentially pumps from the shallow part of the aquifer. The discrete groundwater age distribution model appears to be a suitable approach in settings where the shape of the age distribution cannot be assumed to follow a simple mathematical model, such as a production well field where wells compete for capture area

    Risk assesment of an urban aquifer based on environmental tracers

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    Groundwater from a Pleistocene sandy-gravel aquifer is a drinking water resource for the Union brewery, located nearthe centre of Ljubljana (Slovenia). A large part of the aquifer recharge area is highly urbanized, which represents a greatrisk for the groundwater quality assurance. The groundwater dating techniques were used to study the contaminationrisk of this drinking-water resource. The application of chlorofluorocarbons (CFCs), sulphur hexafluoride (SF6) andtritium-helium-3 (3H-3He) age indicator was tested, as they haven’t been used in Slovene urban areas so far. The resultsreflect that the 3H-3He dating technique is the most suitable for a groundwater age determination in the study urbanaquifer, since SF6 and particularly CFCs concentrations could be affected by the local contaminations. They indicatedthat average groundwater residence times range from 10 to 30 years. Boreholes that are more distant from the Ši{enskihrib hill are more vulnerable to contamination due to flow of young groundwater from a direction of the main aquifer,which is exposed to the urban pollution. The presented results were supplemented with chemical investigations ofgroundwater organic pollutants. An unknown trace organic pollutant with a base ion mass-to-charge ratio 147 was putinto focus. Its identification based on chromatographic separation and a mass spectrometric detection with GC-MS,LC-MS and LC-TOF MS techniques. The newly detected trace organic pollutant in sampled groundwater representstogether with the 3H and 3He data a new technique to study the flow paths and contaminant transport in the urbanaquifer in both, the lateral and vertical directions

    The transient distributions of nuclear weapon-generated tritium and its decay product 3^3He in the Mediterranean Sea, 1952–2011, and their oceanographic potential

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    International audienceWe present a comprehensive account of tritium and 3He in the Mediterranean Sea since the appearance of the tritium generated by the atmospheric nuclear-weapon testing in the 1950s and early 1960s, based on essentially all available observations. Tritium in surface waters rose to 20–30 TU in 1964 (TU = 1018^{18} × [3^3H]/H]), a factor of about 100 above the natural level, and thereafter declined 30-fold up to 2011. The decline was largely due to radioactive tritium decay, which produced significant amounts of its stable daughter 3^3He. We present the scheme by which we separate the tritiugenic part of 3^3He and the part due to release from the sea floor (terrigenic part). We show that the tritiugenic component can be quantified throughout the Mediterranean waters, typically to a ± 0.15 TU equivalent, mostly because the terrigenic part is low in 3^3He. This fact makes the Mediterranean unique in offering a potential for the use of tritiugenic 3^3He as a tracer. The transient distributions of the two tracers are illustrated by a number of sections spanning the entire sea and relevant features of their distributions are noted. By 2011, the 3^3He concentrations in the top few hundred metres had become low, in response to the decreasing tritium concentrations combined with a flushing out by the general westward drift of these waters. Tritium-3^3He ages in Levantine Intermediate Water (LIW) were obtained repeated in time at different locations, defining transit times from the LIW source region east of Rhodes. The ages show an upward trend with the time elapsed since the surface-water tritium maximum, which arises because the repeated observations represent increasingly slower moving parts of the full transit time spectrum of LIW. The transit time dispersion revealed by this new application of tritium-3^3He dating is considerable. We find mean transit times of 12 ± 2 yr up to the Strait of Sicily, 18 ± 3 yr up to the Tyrrhenian Sea, and 22 ± 4 yr up into the Western Mediterranean. Furthermore, we present full Eastern Mediterranean sections of terrigenic 3He and tritium-3He age in 1987, the latter one similarly showing an effect of the transit time dispersion. We conclude that the available tritium and 3He data, particularly if combined with other tracer data, are useful for constraining the subsurface circulation and mixing of the Mediterranean Sea

    Using environmental tracers to determine the relative importance of travel times in the unsaturated and saturated zones for the delay of nitrate reduction measures

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    Groundwater quality in many regions with intense agriculture has deteriorated due to the leaching of nitrate and other agricultural pollutants. Modified agricultural practices can reduce the input of nitrate to groundwater bodies, but it is crucial to determine the time span over which these measures become effective at reducing nitrate levels in pumping wells. Such estimates can be obtained from hydrogeological modeling or lumped-parameter models (LPM) in combination with environmental tracer data. Two challenges in such tracer-based estimates are (i) accounting for the different modes of transport in the unsaturated zone (USZ), and (ii) assessing uncertainties. Here we extend a recently published Bayesian inference scheme for simple LPMs to include an explicit USZ model and apply it to the Dünnerngäu aquifer, Switzerland. Compared to a previous estimate of travel times in the aquifer based on a 2D hydrogeological model, our approach provides a more accurate assessment of the dynamics of nitrate concentrations in the aquifer. We find that including tracer measurements (³H/³He, ⁸⁵Kr, ³⁹Ar, ⁴He) reduces uncertainty in nitrate predictions if nitrate time series at wells are not available or short, but does not necessarily lead to better predictions if long nitrate time series are available. Additionally, the combination of tracer data with nitrate time series allows for a separation of the travel times in the unsaturated and saturated zone

    Upwelling and associated heat flux in the equatorial Atlantic inferred from helium isotope disequilibrium

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    International audienceUpwelling velocities w in the equatorial band are too small to be directly observed. Here, we apply a recently proposed indirect method, using the observed helium isotope (3He or 4He) disequilibria in the mixed layer. The helium data were sampled from three cruises in the eastern tropical Atlantic in September 2005 and June/July 2006. A one-dimensional two-box model was applied, where the helium air-sea gas exchange is balanced by upwelling from 3He-rich water below the mixed layer and by vertical mixing. The mixing coefficients Kv were estimated from microstructure measurements, and on two of the cruises, Kv exceeded 1 × 10−4 m2/s, making the vertical mixing term of the same order of magnitude as the gas exchange and the upwelling term. In total, helium disequilibrium was observed on 54 stations. Of the calculated upwelling velocities, 48% were smaller than 1.0 × 10−5 m/s, 19% were between 1.0 and 2.0 × 10−5 m/s, 22% were between 2.0 and 4.0 × 10−5 m/s, and on 11% of upwelling velocities exceeded this limit. The highest upwelling velocities were found in late June 2006. Meridional upwelling distribution indicated an equatorial asymmetry with higher vertical velocities between the equator and 1° to 2° south compared to north of the equator, particularly at 10°W. Associated heat flux into the mixed layer could be as high as 138 W/m2, but this depends strongly on the chosen depths where the upwelled water comes from. By combining upwelling velocities with sea surface temperature and productivity distributions, a mean monthly equatorial upwelling rate of 19 Sv was estimated for June 2006 and a biweekly mean of 24 Sv was estimated for September 2005
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