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Marine Mg-evaporites are a small oceanic sink of magnesium, precipitating only from extremely evaporated brines. The isotopic composition of Mg in seawater, δ26Mgseawater, has recently been shown to be an effective tool for reconstructing the Mg budget of the modern and past oceans. However, estimations of the Mg isotope fractionation between the Mg-evaporites and their precipitating solution are required for full quantification of the isotope effect of the evaporitic sink on δ26Mgseawater, as well as for utilizing ancient evaporitic sequences as an archive for past δ26Mgseawater. Here, we estimate the Mg isotope fractionation between Mg-evaporites and modern marine-derived brine along the course of seawater evaporation, up to degree evaporation of >200. The sequence of Mg-salts included epsomite (MgSO4·7H2O), kainite (KMgClSO4·3H2O), carnallite (KMgCl3·6H2O), kieserite (MgSO4·H2O) and bischofite (MgCl2·6H2O). The following isotope fractionation values, either negative or positive, were calculated from the isotope difference between the salt and its precipitating brine, and from the evolution of δ26Mg in the brine throughout the evaporation: Δcarnallite-brine = +1.1‰, Δepsomite-brine = +0.59‰, Δbischofite-brine = +0.33‰, Δkieserite-brine = −0.2‰ and Δkainite-brine = −1.3‰. Magnesium isotopic compositions determined on minerals from different ages in the geological record corroborate well these results. Due to precipitation of multi-mineral assemblages having isotope fractionation values of opposing signs, the δ26Mg value of the brine changes only slightly (50%). The isotope fractionations are shown to correlate with the number of water molecules coordinated to the Mg2+ and with Mg-O bond length in the mineral lattice. Given these isotope fractionations, it is calculated that a volume of 0.4 · 106–0.8 · 106 Km3 of a mono-mineral assemblage of kainite or carnallite needs to precipitate in order to change seawater δ26Mg by only 0.1‰. This huge volume is by far larger than the volume of these minerals known to date in the global geological record. Therefore, it is concluded that the impact of Mg-evaporites formation on δ26Mgseawater has been insignificant since the Proterozoic. The results of this study suggest that the Mg isotopic composition of Mg-evaporites preserved in the geological record of evaporitic basins may be used to: 1) quantify geochemical processes that fractionate Mg-isotopes within these basins, such as dolomitization; and 2) complete the secular variations curve of the marine δ26Mg record using basins with well-established evaporitic sequences., Geochimica et Cosmochimica Acta, 301, ISSN:0016-7037, ISSN:1872-9533

The freshwater of the Judea Group aquifer that recharges on the crest of the Judea and Samria Mountain ridge flows east and west, defining two groundwater basins. At the foothills of both basins the freshwater encounters ancient saline or brackish water. The mode of interaction between the two water bodies within each basin is different, although both eventually discharge as brackish spring system. We describe these systems and identify the source of the higher salinity end members.

International audience; Soil aquifer treatment (SAT) systems utilize infiltration basins for recharging pre-treated effluent into the aquifer for water quality improvement. The present research focuses on the diurnal and seasonal variations of oxygen, carbon and nitrogen species in the infiltration basins and in the uppermost vadose zone for determining the impact of different environmental conditions on the composition of the infiltrating effluent. The study was conducted in one of the infiltration basins of the Dan Region Sewage Reclamation Project (Shafdan), Israel. Solar radiation and aeration were recognized to be the two main factors controlling the chemical composition of the effluent within the basin and the uppermost vadose zone. The effluent entering the basin show initial enrichment with dissolved oxygen (DO) due to gas exchange caused by "injection'' through the inlet fountain and turbulence during basin filling. The DO, pH and dissolved inorganic carbon (DIC) fluctuate diurnally as a result of intense in-basin daylight photosynthesis and nighttime respiration. DO and pH increase during day and decrease during night and the DIC shows an opposite behavior. The daylight net primary production was similar to 240 mu mol L-1 d(-1) and the diurnal respiration rate was similar to 430 mu mol L-1 d(-1) (assuming that the nighttime respiration rate is constant over a whole diurnal cycle). The gross primary production during daylight was similar to 450 mu mol L-1 d(-1). Dissolved organic carbon (DOC) and inorganic nitrogen species (NH4+ + NO3) varied significantly in the uppermost vadose zone, however, neither the vadose zone nor the basin showed diurnal fluctuations. It appears that chemical variations between three sampling campaigns conducted in different seasons stemmed mainly from the efficiency of basin aeration that resulted from changes in basin's operation regime and local environmental conditions. The results of this study lead to the following basin management recommendations: (1) keeping short flooding and drying cycles and allowing complete basin desiccation before the next flooding; and (2) flooding the basin during daytime, starting at dawn to maximize oxygen production and minimize infiltration during nighttime. Following these routines would result in higher redox potential of the infiltrating effluent.