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Radiocarbon decay is rarely used to assess the residence time of modern groundwater due to the low resolution of its long half-life in comparison to the expected range of ages. Nonetheless, the modern 14C peak induced by the nuclear bomb tests traces efficiently the impacts of recent human activities on groundwater recharge, as well as for tritium. A simple lumped parameter model (LPM) was implemented in order to assess the interest of 14C and 3H nuclear peaks in a highly anthropized aquifer system of southeastern Spain under intense agricultural development. It required i) to assess a correction factor for modern 14C activities and ii) to reconstruct the 3H recharge input function, affected by irrigation. In such a complex hydrogeological context, an exponential model did not provide satisfying results for all samples. A better solution was reached by taking into account the qualitative recent variation of the recharge rates into a combined exponential flow and piston flow model. Apart from presenting an uncommon approach for 14C dating of modern groundwater, this study highlights the need of considering not only the variation of the tracer but also the variability of recharge rates in LPMs.

We studied a 12.6-m-long sequence from Lake Abiyata (Central Ethiopia) to establish a reliable and accurate chronology for use in global paleoclimatic reconstructions. The 26 accelerator mass spectrometry radiocarbon (AMS 14C) ages, performed on carbonates and organic matter, define 2 parallel chronologies, representing the complete Holocene period. However, these chronologies show a significant discrepancy from 500 to 900 BP in depth; ages obtained on carbonates were always older than those on organic matter. The hydrogeological and geochemical behavior of the Lake Abiyata basin has shed light on this discrepancy. We found that the carbonate crystallization is due mainly to the mixing of lake waters with groundwaters from the multi-layered aquifer contained in the 600-m-thick basement of the lake. The 14C activity of total dissolved inorganic carbon (TDIC) measured by AMS from bottom and surface lake waters (111.4 and 111.8 pMC, respectively) confirms that the mixing occurs at the water-sediment interface. This evidence of groundwater participation in the carbonate crystallization calls into question the current paleoclimatic reconstructions based on inorganic carbonates in lakes. Specific attention should thus be given to the respective proportions of each end-member in the mixing for the quantitative estimation of the groundwater input. This will help to validate the paleoenvironmental reconstructions and to highlight an eventual diagenetical evolution of inorganic carbonates during burial, via the study of pore waters.