4.7 Article

The impact of atmospheric pCO2 on carbon isotope ratios of the atmosphere and ocean

Journal

GLOBAL BIOGEOCHEMICAL CYCLES
Volume 29, Issue 3, Pages 307-324

Publisher

AMER GEOPHYSICAL UNION
DOI: 10.1002/2014GB004929

Keywords

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Funding

  1. Canadian Institute For Advanced Research (CIFAR)
  2. Natural Sciences and Engineering Research Council of Canada (NSERC)
  3. National Research Foundation of Korea [NRF-2013R1A1A1058203]
  4. United Kingdom NERC [NE/K00901X/1]
  5. Carbon Mitigation Initiative (CMI) project at Princeton University - B.P.
  6. National Research Foundation of Korea [2013R1A1A1058203] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. Natural Environment Research Council [NE/K00901X/1] Funding Source: researchfish
  8. NERC [NE/K00901X/1] Funding Source: UKRI

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It is well known that the equilibration timescale for the isotopic ratios C-13/C-12 and C-14/C-12 in the ocean mixed layer is on the order of a decade, 2 orders of magnitude slower than for oxygen. Less widely appreciated is the fact that the equilibration timescale is quite sensitive to the speciation of dissolved inorganic carbon (DIC) in the mixed layer, scaling linearly with the ratio DIC/CO2, which varies inversely with atmospheric pCO(2). Although this effect is included in models that resolve the role of carbon speciation in air-sea exchange, its role is often unrecognized, and it is not commonly considered in the interpretation of carbon isotope observations. Here we use a global three-dimensional ocean model to estimate the redistribution of the carbon isotopic ratios between the atmosphere and ocean due solely to variations in atmospheric pCO(2). Under Last Glacial Maximum (LGM) pCO(2), atmospheric Delta C-14 is increased by approximate to 30 parts per thousand due to the speciation change, all else being equal, raising the surface reservoir age by about 250 years throughout most of the ocean. For C-13, enhanced surface disequilibrium under LGM pCO(2) causes the upper ocean, atmosphere, and North Atlantic Deep Water delta C-13 to become at least 0.2 parts per thousand higher relative to deep waters ventilated by the Southern Ocean. Conversely, under high pCO(2), rapid equilibration greatly decreases isotopic disequilibrium. As a result, during geological periods of high pCO(2), vertical Delta C-13 gradients may have been greatly weakened as a direct chemical consequence of the high pCO(2), masquerading as very well ventilated or biologically dead Strangelove Oceans. The ongoing anthropogenic rise of pCO(2) is accelerating the equilibration of the carbon isotopes in the ocean, lowering atmospheric Delta C-14 and weakening delta C-13 gradients within the ocean to a degree that is similar to the traditional fossil fuel Suess effect.

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