Oceanic sinks for atmospheric CO2

Citation
Ja. Raven et Pg. Falkowski, Oceanic sinks for atmospheric CO2, PL CELL ENV, 22(6), 1999, pp. 741-755
Citations number
156
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
PLANT CELL AND ENVIRONMENT
ISSN journal
01407791 → ACNP
Volume
22
Issue
6
Year of publication
1999
Pages
741 - 755
Database
ISI
SICI code
0140-7791(199906)22:6<741:OSFAC>2.0.ZU;2-5
Abstract
There is approximately 50 times more inorganic carbon in the global ocean t han in the atmosphere. On time scales of decades to millions of years, the interaction between these two geophysical fluids determines atmospheric CO2 levels. During glacial periods, for example, the ocean serves as the major sink for atmospheric CO2, while during glacial-interglacial transitions, i t is a source of CO2 to the atmosphere. The mechanisms responsible for dete rmining the sign of the net exchange of CO2 between the ocean and the atmos phere remain unresolved. There is evidence that during glacial periods, phy toplankton primary productivity increased, leading to an enhanced sedimenta tion of particulate organic carbon into the ocean interior. The stimulation of primary production in glacial episodes can be correlated with increased inputs of nutrients limiting productivity, especially aeolian iron. Iron d irectly enhances primary production in high nutrient (nitrate and phosphate ) regions of the ocean, of which the Southern Ocean is the most important. This trace element can also enhance nitrogen fixation, and thereby indirect ly stimulate primary production throughout the low nutrient regions of the central ocean basins. While the export flux of organic carbon to the ocean interior was enhanced during glacial periods, this process does not fully a ccount for the sequestration of atmospheric CO2. Heterotrophic oxidation of the newly formed organic carbon, forming weak acids, would have hydrolyzed CaCO3 in the sediments, increasing thereby oceanic alkalinity which, in tu rn, would have promoted the drawdown of atmospheric CO2. This latter mechan ism is consistent with the stable carbon isotope pattern derived from air t rapped in ice cores. The oceans have also played a major role as a sink for up to 30% of the anthropogenic CO2 produced during the industrial revoluti on. In large Dart this is due to CO2 solution in the surface ocean; however , some, poorly quantified fraction is a result of increased new production due to anthropogenic inputs of combined N, P and Fe. Based on 'circulation as usual', models predict that future anthropogenic CO2 inputs to the atmos phere will, in part, continue to be sequestered in the ocean. Human interve ntion (large-scale Fe fertilization; direct CO2 burial in the deep ocean) c ould increase carbon sequestration in the oceans, but could also result in unpredicted environmental perturbations. Changes in the oceanic thermohalin e circulation as a result of global climate change would greatly alter the predictions of C sequestration that are possible on a 'circulation as usual ' basis.