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Production and accumulation of calcium carbonate in the ocean: Budget of a nonsteady state
Author(s) -
Milliman John D.
Publication year - 1993
Publication title -
global biogeochemical cycles
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.512
H-Index - 187
eISSN - 1944-9224
pISSN - 0886-6236
DOI - 10.1029/93gb02524
Subject(s) - aragonite , calcite , foraminifera , geology , carbonate , seawater , oceanography , calcium carbonate , diagenesis , carbonate compensation depth , reef , waves and shallow water , mineralogy , benthic zone , chemistry , organic chemistry
Present‐day production of CaCO 3 in tne world ocean is calculated to be about 5 billion tons (bt) per year, of which about 3 bt accumulate in sediments; the other 40% is dissolved. Nearly half of the carbonate sediment accumulates on reefs, banks, and tropical shelves, and consists largely of metastable aragonite and magnesian calcite. Deep‐sea carbonates, predominantly calcitic coccoliths and planktonic foraminifera, have orders of magnitude lower productivity and accumulation rates than shallow‐water carbonates, but they cover orders of magnitude larger basin area. Twice as much calcium is removed from the oceans by present‐day carbonate accumulation as is estimated to be brought in by rivers and hydrothermal activity (1.6 bt), suggesting that outputs have been overestimated or inputs underestimated, that one or more other inputs have not been identified, and/or that the oceans are not presently in steady state. One “missing” calcium source might be groundwater, although its present‐day input is probably much smaller than that of rivers. If, as seems likely, CaCO 3 accumulation presently exceeds terrestial and hydrothermal input, this imbalance presumably is offset by decreased accumulation and increased input during lowered sea level: shallow‐water accumulation decreases by an order of magnitude with a 100 m drop in sea level, while groundwater influx increases because of heightened piezometric head and the diagenesis of metastable aragonite and magnesian calcite from subaerially exposed shallow‐water carbonates.

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