Kinetic isotopic fractionation during carbonate dissolution in laboratory experiments: Implications for detection of microbial CO 2 signatures using δ 13C-DIC

Abstract

Laboratory experiments on reagent-grade calcium carbonate and carbonate rich glacial sediments demonstrate previously unreported kinetic fractionation of carbon isotopes during the initial hydrolysis and early stages of carbonate dissolution driven by atmospheric CO 2. There is preferential dissolution of Ca 12CO 3 during hydrolysis, resulting in δ 13C-DIC values that are significantly lighter isotopically than the bulk carbonate. The fractionation factor for this kinetic isotopic effect is defined as ε carb. ε carb is greater on average for glacial sediments (−17.4‰) than for calcium carbonate (−7.8‰) for the < 63 μm size fraction, a sediment concentration of 5 g L −1 and closed system conditions at 5°C. This difference is most likely due to the preferential dissolution of highly reactive ultra-fine particles with damaged surfaces that are common in subglacial sediments. The kinetic isotopic fractionation has a greater impact on δ 13C-DIC at higher CaCO 3:water ratios and is significant during at least the first 6 h of carbonate dissolution driven by atmospheric CO 2 at sediment concentrations of 5 g L −1. Atmospheric CO 2 dissolving into solution following carbonate hydrolysis does not exhibit any significant equilibrium isotopic fractionation for at least ∼ 6 h after the start of the experiment at 5°C. This is considerably longer than previously reported in the literature. Thus, kinetic fractionation processes will likely dominate the δ 13C-DIC signal in natural environments where rock:water contact times are short <6–24 h (e.g., glacial systems, headwaters in fluvial catchments) and there is an excess of carbonate in the sediments. It will be difficult apply conventional isotope mass balance techniques in these types of environment to identify microbial CO 2 signatures in DIC from δ 13C-DIC data.