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AGU: Global Biogeochemical Cycles

 

Index Terms

  • Atmospheric Composition and Structure: Constituent sources and sinks
  • Atmospheric Composition and Structure: Biosphere/atmosphere interactions
  • Global Change: Biogeochemical processes
  • Global Change: Atmosphere

Abstract

GLOBAL BIOGEOCHEMICAL CYCLES, VOL. 18, GB2002, 18 PP., 2004
doi:10.1029/2003GB002156

Transient simulations of Holocene atmospheric carbon dioxide and terrestrial carbon since the Last Glacial Maximum

Fortunat Joos

Climate and Environmental Physics, Physics Institute, University of Bern, Bern, Switzerland

Stefan Gerber

Climate and Environmental Physics, Physics Institute, University of Bern, Bern, Switzerland

I. C. Prentice

Department of Earth Sciences, University of Bristol, Bristol, UK

Bette L. Otto-Bliesner

National Center for Atmospheric Research, Boulder, Colorado, USA

Paul J. Valdes

School of Geographical Sciences, University of Bristol, Bristol, UK

Conflicting hypotheses are investigated for the observed atmospheric CO2 increase of 20 ppm between 8 ka BP and pre-industrial time. The carbon component of the Bern Carbon Cycle Climate (Bern CC) model, which couples the Lund-Potsdam-Jena Dynamic Global Vegetation Model to an atmosphere-ocean-sediment component, is driven by climate fields from time-slice simulations of the past 21 ka with the Hadley Centre Unified Model or the NCAR Climate System Model. The entire Holocene ice core record of CO2 is matched within a few ppm for the standard model setup, and results are broadly consistent with proxy data of atmospheric 13CO2, mean ocean δ13C, and pollen data, within their uncertainties. Our analysis suggests that a range of mechanisms, including calcite compensation in response to earlier terrestrial uptake, terrestrial carbon uptake and release, SST changes, and coral reef buildup, contributed to the 20 ppm rise. The deep sea δ13C record constrains the contribution of the calcite compensation mechanism to 4–10 ppm. Terrestrial carbon inventory changes related to climate and CO2 forcing, the greening of the Sahara, peat buildup, and land use have probably influenced atmospheric CO2 by a few ppm only. The early Holocene CO2 decrease is quantitatively explained by terrestrial uptake and calcite compensation in response to terrestrial uptake during the glacial-interglacial transition. The recent hypothesis by Ruddiman [2003] that anthropogenic land use caused a 40 ppm CO2 anomaly over the past 8 ka, preventing the climate system from entering a new glacial, would imply an anthropogenic emission of 700 GtC and a decrease in atmospheric δ13C of 0.6 permil. This is not compatible with the ice core δ13C record and would require an upward revision of land use emission estimates by a factor of 3 to 4.

Received 24 September 2003; accepted 18 February 2004; published 3 April 2004.

Citation: Joos, F., S. Gerber, I. C. Prentice, B. L. Otto-Bliesner, and P. J. Valdes (2004), Transient simulations of Holocene atmospheric carbon dioxide and terrestrial carbon since the Last Glacial Maximum, Global Biogeochem. Cycles, 18, GB2002, doi:10.1029/2003GB002156.

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