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.