Impact of amorphous precursor phases on magnesium isotope signatures of Mg-calcite

Vasileios Mavromatis, Bettina Purgstaller, Martin Dietzel, Dieter Buhl, Adrian Immenhauser, Jacques Schott

Research output: Contribution to journalArticleResearchpeer-review

Abstract

Various marine calcifiers form exoskeletons via an amorphous calcium carbonate (ACC) precursor phase and magnesium plays an important role in the temporary stabilization of this metastable phase. Thus, the use of Mg isotope ratios of marine biogenic carbonates as a proxy to reconstruct past seawater chemistry calls for a detailed understanding of the mechanisms controlling Mg isotope signatures during the formation and transformation of ACC to the final crystalline carbonate mineral. For this purpose we have investigated the Mg isotope fractionation between (Ca,Mg)CO3 solids and aqueous fluids at 25 °C and pH = 8.3 during (i) the direct precipitation of crystalline Mg-calcite and (ii) the formation of Mg-rich ACC (Mg-ACC) and its transformation to Mg-calcite. The outcome documents that the small Mg isotope fractionation between Mg-ACC and reactive fluid (#x0394;MgACC-fluid26=−1.0±0.1‰) is not preserved during the transformation of the ACCs into Mg-calcite. Following a pronounced isotopic shift accompanying the transformation of Mg-ACC into Mg-calcite, Δ26Mgcalcite-fluid progressively decreases with reaction progress from #x223C;−3.0‰ to #x2212;3.6‰, reflecting both the approach of isotopic equilibrium and the increase of calcite Mg content (to near 20 mol % Mg). In contrast the crystalline Mg-calcite precipitated directly from the reacting fluid, i.e. lacking a discernable formation of an amorphous precursor, exhibits only small temporal variations in Δ26Mgcalcite-fluid which overall is affected by the precipitation kinetics. The values found in this study at the onset of Mg-ACC precipitation for Mg isotope fractionation between Mg-ACC and the fluid (ΔMgACC-fluid26=−1.0‰) and between Mg-ACC and Mg2+(aq) (ΔMgACC-Mg2+(aq)26=+2.0‰) are consistent with the formation of a hydrated Ca nanoporous solid accommodating Mg bicarbonate/carbonate species in combination with hydrated magnesium. This material crossed by percolating channels filled with the reacting fluid easily converts to Mg-rich calcite via exchange and/or dissolution/precipitation reactions. The results of this study provide new insights on the acquisition of the Mg chemical and isotopic signatures by the skeletal marine carbonates precipitated in confined media from strongly supersaturated fluids. They also offer new guides for the interpretation of the isotopic signature of these organisms for paleo-environmental reconstructions.

Original languageEnglish
Pages (from-to)227-236
Number of pages10
JournalEarth and planetary science letters
Volume464
DOIs
Publication statusPublished - 15 Apr 2017

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magnesium isotopes
Calcium Carbonate
calcite
Isotopes
Magnesium
magnesium
signatures
isotope
fluid
fluids
carbonates
Fluids
calcium carbonates
isotopes
calcium carbonate
fractionation
Carbonates
carbonate
Fractionation
Crystalline materials

Keywords

  • amorphous calcium carbonate
  • isotopic fractionation
  • Mg-isotopes

ASJC Scopus subject areas

  • Geophysics
  • Geochemistry and Petrology
  • Earth and Planetary Sciences (miscellaneous)
  • Space and Planetary Science

Cite this

Impact of amorphous precursor phases on magnesium isotope signatures of Mg-calcite. / Mavromatis, Vasileios; Purgstaller, Bettina; Dietzel, Martin; Buhl, Dieter; Immenhauser, Adrian; Schott, Jacques.

In: Earth and planetary science letters, Vol. 464, 15.04.2017, p. 227-236.

Research output: Contribution to journalArticleResearchpeer-review

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abstract = "Various marine calcifiers form exoskeletons via an amorphous calcium carbonate (ACC) precursor phase and magnesium plays an important role in the temporary stabilization of this metastable phase. Thus, the use of Mg isotope ratios of marine biogenic carbonates as a proxy to reconstruct past seawater chemistry calls for a detailed understanding of the mechanisms controlling Mg isotope signatures during the formation and transformation of ACC to the final crystalline carbonate mineral. For this purpose we have investigated the Mg isotope fractionation between (Ca,Mg)CO3 solids and aqueous fluids at 25 °C and pH = 8.3 during (i) the direct precipitation of crystalline Mg-calcite and (ii) the formation of Mg-rich ACC (Mg-ACC) and its transformation to Mg-calcite. The outcome documents that the small Mg isotope fractionation between Mg-ACC and reactive fluid (#x0394;MgACC-fluid26=−1.0±0.1‰) is not preserved during the transformation of the ACCs into Mg-calcite. Following a pronounced isotopic shift accompanying the transformation of Mg-ACC into Mg-calcite, Δ26Mgcalcite-fluid progressively decreases with reaction progress from #x223C;−3.0‰ to #x2212;3.6‰, reflecting both the approach of isotopic equilibrium and the increase of calcite Mg content (to near 20 mol {\%} Mg). In contrast the crystalline Mg-calcite precipitated directly from the reacting fluid, i.e. lacking a discernable formation of an amorphous precursor, exhibits only small temporal variations in Δ26Mgcalcite-fluid which overall is affected by the precipitation kinetics. The values found in this study at the onset of Mg-ACC precipitation for Mg isotope fractionation between Mg-ACC and the fluid (ΔMgACC-fluid26=−1.0‰) and between Mg-ACC and Mg2+(aq) (ΔMgACC-Mg2+(aq)26=+2.0‰) are consistent with the formation of a hydrated Ca nanoporous solid accommodating Mg bicarbonate/carbonate species in combination with hydrated magnesium. This material crossed by percolating channels filled with the reacting fluid easily converts to Mg-rich calcite via exchange and/or dissolution/precipitation reactions. The results of this study provide new insights on the acquisition of the Mg chemical and isotopic signatures by the skeletal marine carbonates precipitated in confined media from strongly supersaturated fluids. They also offer new guides for the interpretation of the isotopic signature of these organisms for paleo-environmental reconstructions.",
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AU - Mavromatis, Vasileios

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AU - Immenhauser, Adrian

AU - Schott, Jacques

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N2 - Various marine calcifiers form exoskeletons via an amorphous calcium carbonate (ACC) precursor phase and magnesium plays an important role in the temporary stabilization of this metastable phase. Thus, the use of Mg isotope ratios of marine biogenic carbonates as a proxy to reconstruct past seawater chemistry calls for a detailed understanding of the mechanisms controlling Mg isotope signatures during the formation and transformation of ACC to the final crystalline carbonate mineral. For this purpose we have investigated the Mg isotope fractionation between (Ca,Mg)CO3 solids and aqueous fluids at 25 °C and pH = 8.3 during (i) the direct precipitation of crystalline Mg-calcite and (ii) the formation of Mg-rich ACC (Mg-ACC) and its transformation to Mg-calcite. The outcome documents that the small Mg isotope fractionation between Mg-ACC and reactive fluid (#x0394;MgACC-fluid26=−1.0±0.1‰) is not preserved during the transformation of the ACCs into Mg-calcite. Following a pronounced isotopic shift accompanying the transformation of Mg-ACC into Mg-calcite, Δ26Mgcalcite-fluid progressively decreases with reaction progress from #x223C;−3.0‰ to #x2212;3.6‰, reflecting both the approach of isotopic equilibrium and the increase of calcite Mg content (to near 20 mol % Mg). In contrast the crystalline Mg-calcite precipitated directly from the reacting fluid, i.e. lacking a discernable formation of an amorphous precursor, exhibits only small temporal variations in Δ26Mgcalcite-fluid which overall is affected by the precipitation kinetics. The values found in this study at the onset of Mg-ACC precipitation for Mg isotope fractionation between Mg-ACC and the fluid (ΔMgACC-fluid26=−1.0‰) and between Mg-ACC and Mg2+(aq) (ΔMgACC-Mg2+(aq)26=+2.0‰) are consistent with the formation of a hydrated Ca nanoporous solid accommodating Mg bicarbonate/carbonate species in combination with hydrated magnesium. This material crossed by percolating channels filled with the reacting fluid easily converts to Mg-rich calcite via exchange and/or dissolution/precipitation reactions. The results of this study provide new insights on the acquisition of the Mg chemical and isotopic signatures by the skeletal marine carbonates precipitated in confined media from strongly supersaturated fluids. They also offer new guides for the interpretation of the isotopic signature of these organisms for paleo-environmental reconstructions.

AB - Various marine calcifiers form exoskeletons via an amorphous calcium carbonate (ACC) precursor phase and magnesium plays an important role in the temporary stabilization of this metastable phase. Thus, the use of Mg isotope ratios of marine biogenic carbonates as a proxy to reconstruct past seawater chemistry calls for a detailed understanding of the mechanisms controlling Mg isotope signatures during the formation and transformation of ACC to the final crystalline carbonate mineral. For this purpose we have investigated the Mg isotope fractionation between (Ca,Mg)CO3 solids and aqueous fluids at 25 °C and pH = 8.3 during (i) the direct precipitation of crystalline Mg-calcite and (ii) the formation of Mg-rich ACC (Mg-ACC) and its transformation to Mg-calcite. The outcome documents that the small Mg isotope fractionation between Mg-ACC and reactive fluid (#x0394;MgACC-fluid26=−1.0±0.1‰) is not preserved during the transformation of the ACCs into Mg-calcite. Following a pronounced isotopic shift accompanying the transformation of Mg-ACC into Mg-calcite, Δ26Mgcalcite-fluid progressively decreases with reaction progress from #x223C;−3.0‰ to #x2212;3.6‰, reflecting both the approach of isotopic equilibrium and the increase of calcite Mg content (to near 20 mol % Mg). In contrast the crystalline Mg-calcite precipitated directly from the reacting fluid, i.e. lacking a discernable formation of an amorphous precursor, exhibits only small temporal variations in Δ26Mgcalcite-fluid which overall is affected by the precipitation kinetics. The values found in this study at the onset of Mg-ACC precipitation for Mg isotope fractionation between Mg-ACC and the fluid (ΔMgACC-fluid26=−1.0‰) and between Mg-ACC and Mg2+(aq) (ΔMgACC-Mg2+(aq)26=+2.0‰) are consistent with the formation of a hydrated Ca nanoporous solid accommodating Mg bicarbonate/carbonate species in combination with hydrated magnesium. This material crossed by percolating channels filled with the reacting fluid easily converts to Mg-rich calcite via exchange and/or dissolution/precipitation reactions. The results of this study provide new insights on the acquisition of the Mg chemical and isotopic signatures by the skeletal marine carbonates precipitated in confined media from strongly supersaturated fluids. They also offer new guides for the interpretation of the isotopic signature of these organisms for paleo-environmental reconstructions.

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