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Capturing the global signature of surface ocean acidification during the Palaeocene-Eocene Thermal Maximum

TLDR
The remarkable similarity among records from different ocean regions suggests that the degree of ocean carbonate change was globally near uniform, and attribute the global extent of surface ocean acidification to elevated atmospheric carbon dioxide levels during the main phase of the PETM.
Abstract
Geologically abrupt carbon perturbations such as the Palaeocene-Eocene Thermal Maximum (PETM, approx. 56 Ma) are the closest geological points of comparison to current anthropogenic carbon emissions. Associated with the rapid carbon release during this event are profound environmental changes in the oceans including warming, deoxygenation and acidification. To evaluate the global extent of surface ocean acidification during the PETM, we present a compilation of new and published surface ocean carbonate chemistry and pH reconstructions from various palaeoceanographic settings. We use boron to calcium ratios (B/Ca) and boron isotopes (δ11B) in surface- and thermocline-dwelling planktonic foraminifera to reconstruct ocean carbonate chemistry and pH. Our records exhibit a B/Ca reduction of 30-40% and a δ11B decline of 1.0-1.2‰ coeval with the carbon isotope excursion. The tight coupling between boron proxies and carbon isotope records is consistent with the interpretation that oceanic absorption of the carbon released at the onset of the PETM resulted in widespread surface ocean acidification. The remarkable similarity among records from different ocean regions suggests that the degree of ocean carbonate change was globally near uniform. We attribute the global extent of surface ocean acidification to elevated atmospheric carbon dioxide levels during the main phase of the PETM.This article is part of a discussion meeting issue 'Hyperthermals: rapid and extreme global warming in our geological past'.

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Citations
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Reversed deep-sea carbonate ion basin-gradient during Paleocene-Eocene Thermal Maximum

TL;DR: In this article, the authors show that during the PETM, the deep-sea undersaturation was not homogeneous among the different ocean basins, and demonstrate that deep sea [CO32−] increased from the Atlantic through the Southern Ocean into the Pacific.
Journal ArticleDOI

Ocean Carbon Storage across the middle Miocene: a new interpretation for the Monterey Event.

TL;DR: It is proposed that the Miocene Climatic Optimum was associated with elevated oceanic dissolved inorganic carbon caused by volcanic degassing, global warming, and sea-level rise and this hypothesis cannot explain the multi-Myr lag between the δ13C excursion and global cooling.
Journal ArticleDOI

Proxy evidence for state-dependence of climate sensitivity in the Eocene greenhouse

TL;DR: The geological record is tested by combining a new high-resolution boron isotope-based CO2 record with novel estimates of Global Mean Temperature to find that Equilibrium Climate Sensitivity (ECS) was indeed higher during the warmest intervals of the Eocene, agreeing well with recent model simulations, and declined through theEocene as global climate cooled.
References
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Journal ArticleDOI

Oceanography: anthropogenic carbon and ocean pH.

TL;DR: It is found that oceanic absorption of CO2 from fossil fuels may result in larger pH changes over the next several centuries than any inferred from the geological record of the past 300 million years.
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Abrupt deep-sea warming, palaeoceanographic changes and benthic extinctions at the end of the Palaeocene

TL;DR: A remarkable oxygen and carbon isotope excursion occurred in Antarctic waters near the end of the Palaeocene (~57.33 Myr ago), indicating rapid global warming and oceanographic changes that caused one of the largest deep-sea benthic extinctions of the past 90 million years.
Journal ArticleDOI

Reevaluation of the oxygen isotopic composition of planktonic foraminifera: Experimental results and revised paleotemperature equations

TL;DR: In this paper, Orbulina universa and Globigerina bulloides were used to reexamine temperature:δ18O relationships at 15°-25°C.
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