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Research Article

Evidence for a rapid release of carbon at the Paleocene-Eocene thermal maximum

James D. Wright and Morgan F. Schaller
  1. aDepartment of Earth and Planetary Sciences, Rutgers University, Piscataway, NJ 08854; and
  2. bDepartment of Geological Sciences, Brown University, Providence, RI 02912

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PNAS October 1, 2013 110 (40) 15908-15913; https://doi.org/10.1073/pnas.1309188110
James D. Wright
aDepartment of Earth and Planetary Sciences, Rutgers University, Piscataway, NJ 08854; and
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  • For correspondence: jdwright@rci.rutgers.edu
Morgan F. Schaller
aDepartment of Earth and Planetary Sciences, Rutgers University, Piscataway, NJ 08854; and
bDepartment of Geological Sciences, Brown University, Providence, RI 02912
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  1. Edited* by Wallace S. Broecker, Columbia University, Palisades, NY, and approved August 5, 2013 (received for review May 14, 2013)

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Significance

Calcium carbonate and carbon isotope records from the rhythmically bedded Marlboro Clay, deposited during the onset of the PETM CIE, show that the massive release of isotopically light carbon was instantaneous, providing important constraints for the magnitude of carbon released and potential mechanisms.

Abstract

The Paleocene/Eocene thermal maximum (PETM) and associated carbon isotope excursion (CIE) are often touted as the best geologic analog for the current anthropogenic rise in pCO2. However, a causal mechanism for the PETM CIE remains unidentified because of large uncertainties in the duration of the CIE’s onset. Here, we report on a sequence of rhythmic sedimentary couplets comprising the Paleocene/Eocene Marlboro Clay (Salisbury Embayment). These couplets have corresponding δ18O cycles that imply a climatic origin. Seasonal insolation is the only regular climate cycle that can plausibly account for δ18O amplitudes and layer counts. High-resolution stable isotope records show 3.5‰ δ13C decrease over 13 couplets defining the CIE onset, which requires a large, instantaneous release of 13C-depleted carbon. During the CIE, a clear δ13C gradient developed on the shelf with the largest excursions in shallowest waters, indicating atmospheric δ13C decreased by ∼20‰. Our observations and revised release rate are consistent with an atmospheric perturbation of 3,000-gigatons of carbon (GtC).

  • carbon cycle
  • climate change

Footnotes

  • ↵1To whom correspondence should be addressed. E-mail: jdwright{at}rci.rutgers.edu.
  • Author contributions: J.D.W. and M.F.S. designed research, performed research, analyzed data, and wrote the paper.

  • The authors declare no conflict of interest.

  • ↵*This Direct Submission article had a prearranged editor.

  • This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1309188110/-/DCSupplemental.

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Rapid release of carbon at the PETM
James D. Wright, Morgan F. Schaller
Proceedings of the National Academy of Sciences Oct 2013, 110 (40) 15908-15913; DOI: 10.1073/pnas.1309188110

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Rapid release of carbon at the PETM
James D. Wright, Morgan F. Schaller
Proceedings of the National Academy of Sciences Oct 2013, 110 (40) 15908-15913; DOI: 10.1073/pnas.1309188110
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Article Classifications

  • Physical Sciences
  • Earth, Atmospheric, and Planetary Sciences

This article has Letters. Please see:

  • Relationship between Research Article and Letter - February 26, 2014
  • Relationship between Research Article and Letter - February 26, 2014
  • Relationship between Research Article and Letter - February 26, 2014

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  • Rapid release hypothesis for the PETM
    - Feb 26, 2014
Proceedings of the National Academy of Sciences: 110 (40)
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  • Article
    • Abstract
    • Temporal Origin of the Couplets Within the Marlboro Clay
    • Timing of the Onset of the CIE from High-Resolution Stable Isotopes in Millville
    • Surface Water CO2(aq) Concentrations and Carbon Isotopic Equilibrium
    • Reconciling the Marlboro Clay and Deep Ocean Chronologies
    • Atmospheric Response to PETM CIE
    • Implications for the Rate of Carbon Release and Sequence of Events at the PETM
    • Acknowledgments
    • Footnotes
    • References
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