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requirement has led to misunderstandings in the literature. For
example, the future concentration of CO 2 in the atmosphere could reach
a value close to that of the Cretaceous period (145-65 Myr ago), about
2,000 ppmv. However, the Cretaceous period is a geological period
during which calcification was very intense, as proven by the
limestone cliffs of the Pas-de-Calais and Dover, which were formed at
that time. It would, however, be a serious mistake to conclude that
calcification will not be affected in a high-CO 2 future because the
carbonate system will be very different from that of the Cretaceous
period. Seawater with a concentration of dissolved inorganic carbon
(C T ) of 2,400
10 -6 mol kg -1 in equilibrium with an atmosphere with a
concentration of CO 2 of 2,000 ppmv exhibits a calcite saturation state
of 1.1 (at a temperature of 15°C and a salinity of 35). However, the C T
of surface waters in the Cretaceous period were higher (4,900
×
10 -6 mol kg -1 ), and the calcite saturation state was 4.5 (at the same
temperature and salinity). This example, taken from Zeebe and
Ridgwell [ZEE 11], shows that despite their high CO 2 content, the
surface waters of the Cretaceous period were highly favorable to
calcification due to their high saturation in CaCO 3 , which will not be
the case in the future ocean.
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The main reason for which the pH and the saturation of CaCO 3 are
coupled today and in the near future, as opposed to the Cretaceous
period where they were decoupled, is due to CaCO 3 compensation.
The depth of the limit between waters that are saturated and under-
saturated in CaCO 3 (saturation horizon (SH)) is subject to large
vertical changes such that the supply of
CO and of calcium (Ca 2+ )
by rivers are, at equilibrium, equal to the sedimentation of CaCO 3 . If
CaCO 3 deposition is higher than its supply, then the SH moves
upward, exposing a larger area of sediment to corrosive waters and
reducing CaCO 3 burial. In the opposite case, if CaCO 3 deposition is
lower than its supply, the SH moves downward, exposing a smaller
area of sediment to corrosive waters and increasing CaCO 3 burial in
the sediment. This compensation mechanism is very efficient over
timescales longer than 10,000 years [ZEE 11] but does not operate in
the current period of acidification, which is much too fast.
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