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The Melting Is in the Details

Global sea level rises and falls as ice sheets and glaciers melt and grow, providing an integrated picture of the changes in ice volume but little information about how much individual ice fields are contributing to those variations. Knowing the regional structure of ice variability during glaciations and deglaciations will clarify the mechanisms of the glacial cycle. Clark et al. (p. 710) compiled and analyzed more than 5000 radiocarbon and cosmogenic surface exposure ages in order to develop a record of maximum regional ice extent around the time of the Last Glacial Maximum. The responses of the Northern and Southern Hemispheres differed significantly, which reveals how the evolution of specific ice sheets affected sea level and provides insight into how insolation controlled the deglaciation.

Abstract

We used 5704 14C, 10Be, and 3He ages that span the interval from 10,000 to 50,000 years ago (10 to 50 ka) to constrain the timing of the Last Glacial Maximum (LGM) in terms of global ice-sheet and mountain-glacier extent. Growth of the ice sheets to their maximum positions occurred between 33.0 and 26.5 ka in response to climate forcing from decreases in northern summer insolation, tropical Pacific sea surface temperatures, and atmospheric CO2. Nearly all ice sheets were at their LGM positions from 26.5 ka to 19 to 20 ka, corresponding to minima in these forcings. The onset of Northern Hemisphere deglaciation 19 to 20 ka was induced by an increase in northern summer insolation, providing the source for an abrupt rise in sea level. The onset of deglaciation of the West Antarctic Ice Sheet occurred between 14 and 15 ka, consistent with evidence that this was the primary source for an abrupt rise in sea level ~14.5 ka.

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References and Notes

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Published In

Science
Volume 325 | Issue 5941
7 August 2009

Submission history

Received: 27 February 2009
Accepted: 23 June 2009
Published in print: 7 August 2009

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Acknowledgments

The authors thank J. Licciardi, N. Pisias, and an anonymous reviewer for their constructive comments, and J. Bockheim, B. Hall, and P. Huybers for discussions. This work was supported by NSF (P.U.C., J.D.S., A.E.C., and S.W.H.), the Geological Survey of Canada Climate Change Program (A.S.D.), the University of Wisconsin (A.E.C.), the Swedish Nuclear Fuel and Waste Management Co. (B.W.), and the Canadian Institute for Advanced Research (J.X.M.).

Authors

Affiliations

Peter U. Clark* [email protected]
Department of Geosciences, Oregon State University, Corvallis, OR 97331, USA.
Arthur S. Dyke
Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario K1A 0E8, Canada.
Jeremy D. Shakun
Department of Geosciences, Oregon State University, Corvallis, OR 97331, USA.
Anders E. Carlson
Department of Geology and Geophysics, University of Wisconsin, Madison, WI 53706, USA.
Jorie Clark
Department of Geosciences, Oregon State University, Corvallis, OR 97331, USA.
Barbara Wohlfarth
Department of Geology and Geochemistry, Stockholm University, SE-10691, Stockholm, Sweden.
Jerry X. Mitrovica
Department of Earth and Planetary Sciences, Harvard University, Cambridge, MA 02138, USA.
Steven W. Hostetler
U.S. Geological Survey, Department of Geosciences, Oregon State University, Corvallis, OR 97331, USA.
A. Marshall McCabe
School of Environmental Science, University of Ulster, Coleraine, County Londonderry, BT52 1SA, UK.

Notes

*
To whom correspondence should be addressed. E-mail: [email protected]

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