THE WIDESPREAD OCCURRENCE OF COUPLED CARBONATE DISSOLUTION/REPRECIPITATION IN SURFACE SEDIMENTS ON THE BAHAMAS BANK

被引:66
作者
Burdige, David J. [1 ]
Hu, Xinping [1 ]
Zimmerman, Richard C. [1 ]
机构
[1] Old Dominion Univ, Dept Ocean Earth & Atmospher Sci, Norfolk, VA 23529 USA
基金
美国国家科学基金会;
关键词
Bahamas Bank; carbonate dissolution; carbonate reprecipitation; early diagenesis; MAGNESIAN CALCITE OVERGROWTHS; SOUTH FLORIDA PLATFORM; PORE-WATER; NUTRIENT REGENERATION; OCEAN ACIDIFICATION; MARINE DIAGENESIS; ORGANIC-MATTER; DISSOLUTION; ARAGONITE; RECRYSTALLIZATION;
D O I
10.2475/06.2010.03
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Using two complimentary approaches (pore water advection/diffusion/reaction modeling and stable isotope mass balance calculations) we show that carbonate dissolution/reprecipitation occurs on early diagenetic time scales across a broad range of sediments on the Great Bahamas Bank. The input of oxygen into the sediments, which strongly controls sediment carbonate dissolution, has two major sources belowground input by seagrasses (that is, seagrass O-2 pumping), and permeability-driven advective pore water exchange. The relative importance of these O-2 delivery mechanisms depends on both seagrass density, and on how bottom water flow interacts with the seagrass canopy and leads to this advective exchange. Dissolution appears to involve the preferential dissolution of high-Mg calcite, and the rates of dissolution increase linearly with increasing seagrass density. Isotopic evidence of dissolution/reprecipitation is consistent with the occurrence of Ostwald ripening as the mechanism of reprecipitation, in which smaller crystals dissolve and then reprecipitate as larger crystals, with little or no change in mineralogy. Estimates of the aerially-integrated dissolution flux on the Bahamas Bank suggest that carbonate dissolution is an important loss term in the budget of shallow water carbonate sediments, and that on-bank carbonate dissolution, rather than offshore transport, may represent an important sink for gross shallow water carbonate production. Dissolution in carbonate bank and bay sediments may also be a significant alkalinity source to the surface ocean, and should be considered in global alkalinity/carbonate budget. Finally, coupled dissolution/reprecipitation may have a major impact on the stable isotope composition of carbonate sediments that are ultimately preserved in the rock record. These processes may therefore need to be considered, for example, when using carbon isotope records to obtain information on the operation of the global carbon cycle during the Phanerozoic.
引用
收藏
页码:492 / 521
页数:30
相关论文
共 87 条
[1]  
Andersson AJ, 2003, GEOLOGY, V31, P513, DOI 10.1130/0091-7613(2003)031<0513:SOSCAI>2.0.CO
[2]  
2
[3]   Dissolution of carbonate sediments under rising pCO2 and ocean acidification:: Observations from Devil's Hole, Bermuda [J].
Andersson, Andreas J. ;
Bates, Nicholas R. ;
Mackenzie, Fred T. .
AQUATIC GEOCHEMISTRY, 2007, 13 (03) :237-264
[4]  
BARTH NG, 1984, MODERN METHODS PARTI
[5]   MARINE DIAGENESIS OF SHALLOW-WATER CALCIUM-CARBONATE SEDIMENTS [J].
BATHURST, RG .
ANNUAL REVIEW OF EARTH AND PLANETARY SCIENCES, 1974, 2 :257-274
[6]   Relating estimates of CaCO3 production, export, and dissolution in the water column to measurements of CaCO3 rain into sediment traps and dissolution on the sea floor:: A revised global carbonate budget [J].
Berelson, W. M. ;
Balch, W. M. ;
Najjar, R. ;
Feely, R. A. ;
Sabine, C. ;
Lee, K. .
GLOBAL BIOGEOCHEMICAL CYCLES, 2007, 21 (01)
[7]  
BERNER R.A, 2004, The Phanerozoic carbon cycle: CO2 and O2
[8]   STOICHIOMETRIC MODELS FOR NUTRIENT REGENERATION IN ANOXIC SEDIMENTS [J].
BERNER, RA .
LIMNOLOGY AND OCEANOGRAPHY, 1977, 22 (05) :781-786
[9]   INHIBITION OF ARAGONITE PRECIPITATION FROM SUPER-SATURATED SEAWATER - LABORATORY AND FIELD-STUDY [J].
BERNER, RA ;
WESTRICH, JT ;
GRABER, R ;
SMITH, J ;
MARTENS, CS .
AMERICAN JOURNAL OF SCIENCE, 1978, 278 (06) :816-837
[10]   ROLE OF MAGNESIUM IN CRYSTAL-GROWTH OF CALCITE AND ARAGONITE FROM SEA-WATER [J].
BERNER, RA .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1975, 39 (04) :489-&