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Rapid and sustained surface ocean acidification during the Paleocene‐Eocene Thermal Maximum
Author(s) -
Penman Donald E.,
Hönisch Bärbel,
Zeebe Richard E.,
Thomas Ellen,
Zachos James C.
Publication year - 2014
Publication title -
paleoceanography
Language(s) - English
Resource type - Journals
eISSN - 1944-9186
pISSN - 0883-8305
DOI - 10.1002/2014pa002621
Subject(s) - thermocline , geology , ocean acidification , carbonate , oceanography , carbon cycle , paleoceanography , seawater , deep sea , isotopes of carbon , sea surface temperature , carbon dioxide , surface water , total organic carbon , climatology , environmental science , environmental chemistry , ecosystem , chemistry , ecology , organic chemistry , biology , environmental engineering
The Paleocene‐Eocene Thermal Maximum (PETM) has been associated with the release of several thousands of petagrams of carbon (Pg C) as methane and/or carbon dioxide into the ocean‐atmosphere system within ~10 kyr, on the basis of the co‐occurrence of a carbon isotope excursion (CIE), widespread dissolution of deep sea carbonates, and global warming. In theory, this rapid carbon release should have severely acidified the surface ocean, though no geochemical evidence has yet been presented. Using boron‐based proxies for surface ocean carbonate chemistry, we present the first observational evidence for a drop in the pH of surface and thermocline seawater during the PETM. Planktic foraminifers from a drill site in the North Pacific (Ocean Drilling Program Site 1209) show a ~0.8‰ decrease in boron isotopic composition (δ 11 B) at the onset of the event, along with a 30–40% reduction in shell B/Ca. Similar trends in δ 11 B are present in two lower‐resolution records from the South Atlantic and Equatorial Pacific. These observations are consistent with significant, global acidification of the surface ocean lasting at least 70 kyr and requiring sustained carbon release. The anomalies in the B records are consistent with an initial surface pH drop of ~0.3 units, at the upper range of model‐based estimates of acidification.

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