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Book ChapterDOI

Formation and Diagenesis of Carbonate Sediments

Rolf S. Arvidson, +1 more
- 01 Jan 2014 - 
- Vol. 9, pp 61-101
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TLDR
The first edition of this chapter provided a brief review of the geochemistry of carbonate minerals, summarized general aspects of their thermodynamics and the kinetics of their precipitation and dissolution, and then used the natural division between deep-sea marine carbonates (chalks and pelagic muds) versus shoal-water carbonates to organize details of the formation, distribution, and subsequent diagenetic alteration of these phases as mentioned in this paper.
Abstract
The first edition of this chapter provided a brief review of the geochemistry of carbonate minerals, summarized general aspects of their thermodynamics and the kinetics of their precipitation and dissolution, and then used the natural division between deep-sea marine carbonates (chalks and pelagic muds) versus shoal-water carbonates (skeletal and nonskeletal materials) to organize details of the formation, distribution, and subsequent diagenetic alteration of these phases. A substantial focus in this treatment was thus the description of the behavior and fate of carbonate minerals in natural settings. In this chapter, this latter material appears largely unchanged. The aim in this revision is not simply to trudge through calcite, dolomite, and magnesite rate equations, detailed reviews of which are available elsewhere; instead, the intent is to provide background for the selective discussion of recent work on carbonate mineral surfaces (mostly calcite).

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Citations
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Abandoned mine sites as a source of contamination by heavy metals: A case study in a semi-arid zone

TL;DR: In this paper, the dispersion and influence of soluble and particulate metals present in the materials from an abandoned mine, Cabezo Rajao, in SE Spain, was evaluated.
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Magnetic mineral diagenesis

TL;DR: In this paper, the authors provide a treatment for the full range of diagenetic environments, including oxic, manganiferous, ferruginous, and methanic.
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Diagenetic uptake of rare earth elements by bioapatite, with an example from Lower Triassic conodonts of South China

TL;DR: In this article, the authors review existing literature on the diagenetic fluxes of rare earth elements (REEs) in marine sediments and porewaters in order to systematize existing knowledge on this subject.
Book ChapterDOI

Coral Reefs and Changing Seawater Carbonate Chemistry

TL;DR: In this article, the relationship between seawater carbonate chemistry and coral reef calcification is discussed, identifying the hurdles in understanding the two, and presenting a strategy for overcoming those hurdles.
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Diagenetically induced shear failure of fine-grained sediments and the development of polygonal fault systems

TL;DR: In this article, the authors suggest that diagenesis of clay-rich sediments can lead to shear failure under low confining stresses, and this has significant implications for shale gas exploration, CO2 sequestration and exploration for methane hydrates.
References
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Journal ArticleDOI

The Growth of Crystals and the Equilibrium Structure of their Surfaces

TL;DR: In this paper, it was shown that the rate of growth of a surface containing dislocations is proportional to the square of the supersaturation for low values and to the first power for high values of the latter.
Journal ArticleDOI

SUPCRT92: a software package for calculating the standard molal thermodynamic properties of minerals, gases, aqueous species, and reactions from 1 to 5000 bar and 0 to 1000 ° C

TL;DR: The SUPCRT92 software package as discussed by the authors is a suite of three interactive FORTRAN 77 programs, including SPRONS92.DAT, which allows the calculation of the standard Gibbs free energy, enthalpy, entropy, heat capacity, and volume of each reaction specified on the RXN file through a range of conditions specified on CON file.
Journal ArticleDOI

The solubilities of calcite, aragonite and vaterite in CO2-H2O solutions between 0 and 90°C, and an evaluation of the aqueous model for the system CaCO3-CO2-H2O

TL;DR: In this paper, the authors compared the solubility of calcite, aragonite, and vaterite in CO2-H2O solutions between 0 and 90°C using the Debye-Huckel individual ion activity coefficients.
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