This research explores weathering processes influencing atmospheric CO2 and deepening CCD through magnesium isotopes during the Eocene-Oligocene Transition.
During the Eocene‐Oligocene Transition (ca. 34 Ma), the Earth underwent a dramatic decline in atmospheric CO 2 , global cooling, a deepening of the carbonate compensation depth (CCD), and the formation of a permanent ice sheet on Antarctica. The expansion of Antarctic glaciers eroded the underlying bedrock and increased the weathering flux to the ocean. However, the role silicate and carbonate weathering play in atmospheric CO 2 removal and the CCD through Ca 2+ and alkalinity production is poorly understood. Magnesium isotopes (δ 26 Mg) are fractionated during carbonate and clay mineral formation and can be used to quantify the relative flux from silicate and carbonate weathering. Here, we report the δ 26 Mg composition of the carbonate, reactive (ferromanganese coatings), and residual (silicate) fraction of marine sediments from the Kerguelen Plateau (Ocean Drilling Program Site 738), near a major drainage system of the East Antarctic Ice Sheet, to explore the response of subglacial and shelf weathering to ice sheet expansion. The δ 26 Mg of the carbonate fraction (−2.29‰ to −0.95‰), reactive fraction (−0.36‰ to 0.10‰), and residual fraction (−0.05‰ to 0.55‰) display similar values to surface‐dwelling calcareous nannofossils, deep‐water ferromanganese nodules, and Antarctic bedrock, respectively. Isotope fluctuations in all three phases suggest that the formation of the Antarctic ice sheet drove efficient chemical weathering of underlying silicate bedrock, which was rapidly transported to the Southern Ocean, resulting in further CO 2 drawdown, while a local sea‐level low stand exposed carbonates on the Antarctic continental shelf to weathering, contributing to a deepening of the CCD.
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Sproson et al. (2026) studied this question.
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