In stratified hardwater lakes, calcite crystallization in the epilimnion and partial dissolution in the hypolimnion play important roles in the cycling of Ca2+ in the water column. Mg2+ and Sr2+ coprecipitate with this mineral, to be released together with Ca2+ upon its dissolution. Here, we focus on Lake Kinneret (Sea of Galilee, Israel), a stratified, warm, hardwater lake, searching for an interpretable, high resolution picture of the processes that drive Ca2+, Mg2+ and Sr2+cycling in this and similar lakes elsewhere.In total, 1428 water samples were collected from the lake, and another 81 samples were collected from the Jordan River and two small streams discharging into it, covering a full monomictic cycle from December 2001 through March 2003. Particulate material was retrieved from sediment traps in the hypolimnion. The water samples were analyzed for Na+, K+, Mg2+, Ca2+, Sr2+, Cl−, SO42−, HCO3− and Br−, and the trapped particulates were examined under SEM and analyzed for their Ca, Mg, and Sr content. Individual calcite crystals within the particulate material underwent LA-ICP-MS analysis for Ca, Mg, and Sr.Downward transport of Ca2+ involves crystallization of calcite in the epilimnion, followed by its settling through the water column, followed by its partial dissolution in the hypolimnion. Magnesium and Sr2+ follow Ca2+ by coprecipitation in calcite and are released upon its dissolution in the hypolimnion. Upward cycling of the three solutes occurs through an admixture of the hypolimnetic water into the epilimnion during thermocline deepening, terminated by overturn of the lake.Removal rates of Mg2+ and Sr2+ from the lake, relative to that of Ca2+, and the water–calcite distribution coefficients, DMg and DSr, were calculated from the analyses using: (1) epilimnion water and ‘bulk’ particulates; (2) epilimnion water only; and (3) epilimnion water and calcite crystals in the particulates. The DSr values obtained were internally consistent (0.194±5.9%, 0.22–0.28, and 0.204–0.232, respectively); however, the DMg value for the ‘bulk’ particulates (0.0477) was ∼6 times higher than that corresponding to calcite crystals included therein (0.00841). This difference is attributed to phytoplankton debris in the ‘bulk’ particulates and should be of concern to geochemists using Mg/Ca ratios in limestone to reconstruct ancient aquatic environments.The cycling of Ca2+, Mg2+ and Sr2+ in the stratified lake is monitored by Mg/Ca vs. Sr/Ca regression diagrams, where each line represents the water column composition on a specific date. The distance of the data points from the initial (mixed lake) coordinates reflects the fractionation of Ca2+, Mg2+ and Sr2+ after the onset of stratification. The regression lines rotate in an orderly anticlockwise direction in response to the high calcite flux from the epilimnion in spring and the higher rate of Mg2+ replenishment than that of Sr2+, compensating for their loss in calcite. The release of Mg2+ and Sr2+ from dissolving calcite in the hypolimnion, at an Mg/Sr ratio (7.5eq/eq) much lower than that in the surrounding water (∼160eq/eq), lends additional support to the anticlockwise rotation. Reversal of rotation occurs in summer, when calcite crystallization and the freshwater supply slow down, and brackish and saline water sources take control over the Mg/Sr ratio in the lake. Subsequent turnover and mixing of the lake in winter reset the Mg/Ca and Sr/Ca ratios to their original values before the next stratification.
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