Description: Lake Karakul in the eastern Pamirs is a large and closed-basin lake in a partly glaciated catchment. Two parallel sediment cores were collected from 12 m water depth. The cores were correlated using XRF analysis and dated using radiocarbon and OSL techniques. The age results of the two dating methods are generally in agreement. The correlated composite core of 12.26 m length represents continuous accumulation of sediments in the lake basin since 31 ka. The lake reservoir effect (LRE) remained relatively constant over this period. High sediment accumulation rates (SedARs) were recorded before 23 ka and after 6.5 ka. The relatively close position of the coring location near the eastern shore of the lake implies that high SedARs resulted from low lake levels. Thus, high SedARs and lower lake levels before 23 ka probably reflect cold and dry climate conditions that inhibited the arrival of moist air at high elevation in the eastern Pamirs. Low lake levels after 6.5 ka were probably caused by declining temperatures after the warmer early Holocene, which had caused a reduction in water resources stored as snow, ice and frozen ground in the catchment. Low SedARs during 23–6.5 ka suggest increased lake levels in Lake Karakul. A short-lived increase of SedARs at 15 ka probably corresponds to the rapid melting of glaciers in the Karakul catchment during the Greenland Interstadial 1e, shortly after glaciers in the catchment had reached their maximum extents. The sediment cores from Lake Karakul represent an important climate archive with robust chronology for the last glacial–interglacial cycle from Central Asia.

Description: On a beautiful summer day Emma and Steven want to have fun at their favourite lake. However, a mysterious situation thwarts their plans. This leads the two friends on an unexpected quest ... Join Emma and Steven as they explore the vast, intriguing and efficient world of stable isotopes: What are isotopes? How do isotopes work? And last but not least, how can isotopes help Emma and Steven to finally answer the question: Who poisoned Family Mole?

Description: In this study, to better understand the factors controlling the concentration and isotope composition of lithium (Li) in the ocean, we investigated the behaviour of Li during interaction of kaolinite with artificial seawater. Dissolution of kaolinite in Li-free seawater at acidic conditions (exp. 1) results in a strong preferential release of light Li isotopes, with △7Liaq-kaol ∼ −19‰, likely reflecting both the preferential breaking of 6Lisingle bondO bonds over 7Lisingle bondO bonds and the release of Li from the isotopically lighter AlO6 octahedral sites. Sorption experiments on kaolinite (exp. 2) revealed a partition coefficient between kaolinite and fluid of up to 28, and an isotopic fractionation of −24‰. Thermodynamic calculation indicates authigenic smectites formed from the dissolution of kaolinite in seawater at pH 8.4 (exp. 3). The formation of authigenic phase strongly removed Li from the solution (with a partition coefficient between the solid and the fluid equal to 89) and led to an increase of ca. 25‰ in seawater δ7Li. This fractionation can be described by a Rayleigh fractionation model at the early stage of the experiment during rapid clay precipitation, followed, at longer reaction time, by equilibrium isotope fractionation during the much slower removal of aqueous Li via co-precipitation and adsorption. Both processes are consistent with a fractionation factor between the solid and the aqueous solution of ∼−20‰. These experiments have implications for interpreting the Li isotopic composition of both continental and marine waters. For instance, the preferential release of 6Li observed during kaolinite far-from-equilibrium dissolution could explain the transient enrichments in 6Li observed in soil profiles. With regard to the evolution of seawater δ7Li over geological time scales, our experimental results suggest that detrital material discharged by rivers to the ocean and ensuing “reverse chemical weathering” have the potential to strongly impact the isotopic signature of the ocean through the neoformation of clay minerals.

Description: The stable isotopes of lithium (Li) serve as a robust proxy of silicate weathering. The fate and transport of these isotopes in the dissolved load of major rivers have been characterized to infer changes in both contemporary weathering regimes and paleo-conditions. In this contribution, we deconvolve this integrated signal into the individual processes that fractionate Li at the inception of silicate weathering by directly measuring Li isotope ratios of waters (Li) transiting through a rapidly eroding first-order hillslope. We use these data to develop a multicomponent reactive transport framework, which shows that net dissolution of weathered material generates light Li signatures (as low as −9.2‰) in the shallow portion of the vadose zone. An increase in Li deeper into the vadose zone (as much as +18‰) reflects an increasing contribution of secondary mineral formation. Below the water table, congruent weathering occurs and imparts elevated cation concentrations and bedrock Li. Silicate weathering continues within the saturated zone as groundwater travels downslope (Li = +13 to + 24‰) to the stream. The stream signatures (Li = +28 to +29‰) reflect the terminus of this network of silicate weathering reactions and the relative magnitude of each contributing process (e.g., transitions in secondary mineral formation, dissolution of weathered material). We show that fluid progressing through the weathering profile of this first-order hillslope is distinguished by a sequence of characteristic Li isotope signatures, which can be reproduced in a forward, process-based model framework. This model development offers an improved quantitative basis for the use of metal(loid) stable isotopes in disentangling catchment-scale chemical weathering fluxes.