“…This dilution of radiocarbon-dead CO2 in the atmosphere may well have been complemented by other terrestrial sources such as subglacial paleosol oxidation (Zeng, 2007;Simmons et al, 2016), permafrost-bound organic carbon oxidation (Tesi et al, 2016;Winterfeld et al, 2018;Köhler et al, 2014;Ciais et al, 2012), and by (time-delayed) volcanic emissions due to unloading of the lithosphere (Roth and Joos, 2012). In addition to studies of weathering in glacial forefields and source-to-sink tracing of sedimentary kerogen, several lines of geochemical evidence including atmospheric carbon isotopic composition ( 13 C and 14 C), which have thus far received contorted, partial explanations (Broecker and Clark, 2010;Schmitt et al, 2012;Broecker and McGee, 2013), glacial-interglacial changes in 14 C of dissolved inorganic carbon in seawater (Rafter et al, 2019, c.f., discussions therein), seawater osmium isotope changes, and long-term atmospheric O2 content, conceptually go hand-in-hand with an opening of the exogenous kerogen cycle modulated by glacial activity. While geomagnetic variability and ocean ventilation together struggle to fully explain observed changes in atmospheric radiocarbon (Broecker and Barker, 2007;Cheng et al, 2018), the dilution of atmospheric CO2 by accelerated ancient terrestrial organic carbon oxidation at glacial terminations, in conjunction with other mechanisms including atmosphere-ocean gas exchange (e.g., Sigman et al, 2010;Marcott et al, 2014;Menviel et al, 2018;Martin, 1990;Sarntheim et al, 2013) appears as a simple and plausible explanation.…”