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

Author:

Babila Tali L.12ORCID,Penman Donald E.13,Hönisch Bärbel4,Kelly D. Clay5,Bralower Timothy J.6,Rosenthal Yair27,Zachos James C.1

Affiliation:

1. Department of Earth and Planetary Sciences, University of California Santa Cruz, 1156 High Street, Santa Cruz, CA 95064, USA

2. Department of Marine and Coastal Sciences, Rutgers, The State University of New Jersey, 71 Dudley Road, New Brunswick, NJ 08901 USA

3. Department of Geology and Geophysics, Yale University, 210 Whitney Avenue, New Haven, CT 06511, USA

4. Department of Earth and Environmental Sciences, Lamont-Doherty Earth Observatory of Columbia University, 61 Route 9 W, Palisades, NY 10964, USA

5. Department of Geoscience, University of Wisconsin-Madison, 1215 West Dayton Street, Madison, WI 53706, USA

6. Department of Geosciences, Pennsylvania State University, 503 Deike Building, University Park, PA 16802, USA

7. Department of Earth and Planetary Sciences, Rutgers, The State University of New Jersey, 610 Taylor Road, Piscataway, NJ 08854, USA

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 (δ 11 B) 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 δ 11 B 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’.

Funder

NSF

Flint Postdoctoral Fellowship

Publisher

The Royal Society

Subject

General Physics and Astronomy,General Engineering,General Mathematics

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