Cited by 124Geochemistry and Elemental AnalysisPaleontology and Stratigraphy of FossilsGeological formations and processes

The influence of organic matter in organogenic dolomitization

Slaughter, M., Hill, Ronald J.·1991·Journal of Sedimentary Research

Abstract

We hypothesize that the decomposition of organic debris derived from plants, planktonic animals, and algae by sulfate-reducing bacteria, and specifically by the enzymatic degradation of protein, is vital to organogenic dolomitization. The role of this degradation is to increase both alkalinity and pH of the pore waters, providing the necessary solution and surface chemistries for dolomitization to occur. Ammonia, derived by the enzymatic breakdown of proteins, is the only simple base available to supply the pH conditions necessary for dolomitization. Protein is abundant in organic matter derived from a marine source. Because of the large enthalpies of hydration of Mg (super +2) and Ca (super +2) ions, we propose that dolomitization proceeds with the transfer of neutral ion pairs, CaCO 30 and MgCO 30 , to and from the dolomite surface within a replacement zone. For this reason, dolomitization will occur only when the concentration of the CO 3 (super -2) ion is high and in large excess to the HCO 3 (super -) ion in solution and at the carbonate crystal surface. These conditions will be met when the pH and/or ionic strength is high and the carbonate alkalinity is also high.

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Crossref · 10.1306/d42676f9-2b26-11d7-8648000102c1865d

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  • The main kinetic factors that inhibit the nucleation or precipitation of dolomite at low temperatures are the high hydration energy of the magnesium ion, the presence of sulfate (even in very low concentrations) related to the formation of complex MgSO4^0, and the low activity of CO3 in most natural solutions.

    “the main kinetic factors that inhibit the nucleation or precipitation of dolomite at low temperatures are thought to include: (1) the high hydration energy of the magnesium ion [22,45,51,66,[74][75][76][77][78][79][80]; (2) the presence of sulfate (even in very low concentrations), related to the formation of complex MgSO 4 0 [32,74,81,82]; and (3) the low activity of CO 2- 3 in most natural solut”

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Authors
Slaughter, M., & Hill, R. J.
Affiliations
Colorado School of Mines (US)
Venue
Journal of Sedimentary Research
Published
1991-03-01
Volume
61
Issue
2
Pages
296-303
ISSN
  • 0022-4472 (ISSN-L)
  • 1938-3681
  • 1527-1404
OpenAlex
W2168301466
Cited by
124
References
0
Citations by year
2026: 5 · 2025: 5 · 2024: 2 · 2023: 9 · 2022: 7 · 2021: 4 · 2020: 5 · 2019: 8 · 2018: 3 · 2017: 5 · 2016: 3 · 2015: 3 · 2014: 2 · 2013: 4 · 2012: 8
FWCI
1.25
Type
journal article
Language
en
Open access
closed
Locations
Journal of Sedimentary Research (publishedVersion)
Funders
Japan Society for the Promotion of Science
Topics
  • Physical Sciences › Earth and Planetary Sciences › Geochemistry and Petrology › Geochemistry and Elemental Analysis
  • Physical Sciences › Earth and Planetary Sciences › Paleontology › Paleontology and Stratigraphy of Fossils
  • Physical Sciences › Earth and Planetary Sciences › Earth-Surface Processes › Geological formations and processes
Keywords
organic matter, sulfate-reducing bacteria, protein degradation, ammonia, pore water pH, carbonate alkalinity, dolomite replacement, calcium carbonate, magnesium carbonate, carbonate ions, bicarbonate, ionic strength

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