Carbonate compensation dynamics

被引:43
作者
Boudreau, Bernard P. [1 ]
Middelburg, Jack J. [2 ,3 ]
Meysman, Filip J. R. [2 ,4 ]
机构
[1] Dalhousie Univ, Dept Oceanog, Halifax, NS B3H 4J1, Canada
[2] NIOO KNAW, Ctr Estuarine & Marine Ecol, NL-4401 NT Yerseke, Netherlands
[3] Univ Utrecht, Fac Geosci, Utrecht, Netherlands
[4] Free Univ Brussels, Dept Analyt & Environm Chem, Brussels, Belgium
基金
加拿大自然科学与工程研究理事会;
关键词
DEEP-SEA; DISSOLUTION KINETICS; CALCIUM-CARBONATE; ATMOSPHERIC CO2; OCEAN; PRESERVATION; WATER; MODEL;
D O I
10.1029/2009GL041847
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Carbonate saturation (z(sat)) and compensation (z(cc)) depths change with deep-ocean acidification and basification. We present simple, explicit, mechanistic formulas for the positions of these two critical depths. In particular z(cc) is expressed as a function of the mean dissolved carbonate ion concentration of the deep ocean, [CO3](D), the supply of dissolvable CaCO3, F-c, and the dissolution rate constant at the sediment-water interface, k(c), which we show to be essentially mass-transfer controlled. Calculations reveal that z(sat) and z(cc) are today some similar to 0.9 km apart and will rise and separate by as much as 1.7 km with acidification; conversely, if [CO3](D) increases, z(sat) and z(cc) will deepen, but their separation will asymptote to similar to 0.7 km. Citation: Boudreau, B. P., J. J. Middelburg, and F. J. R. Meysman (2010), Carbonate compensation dynamics, Geophys. Res. Lett., 37, L03603, doi:10.1029/2009GL041847.
引用
收藏
页数:5
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