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Journal ArticleDOI

An isotopic study of siderites, dolomites and ankerites at high temperatures☆

J Rosenbaum, +1 more
- 01 Jun 1986 - 
- Vol. 50, Iss: 6, pp 1147-1150
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TLDR
In this paper, an empirically derived relationship between the chemical composition of a carbonate in the CaCO3-(Ca, Mg)(CO3)2-FeCO3 system and the function 103 In α at 100°C is 103 ∆ α = 8.94XCaCO3 + 9.29XMgCO3+ 8.77XFeCo3 where Xi is the mole percent of component i in the carbonate.
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This article is published in Geochimica et Cosmochimica Acta.The article was published on 1986-06-01. It has received 768 citations till now. The article focuses on the topics: Carbonate & Ankerite.

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Citations
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Fluid inclusion and stable isotope (O, H, C, and S) constraints on the genesis of the Serrinha gold deposit, Gurupi Belt, northern Brazil

TL;DR: The Serrinha gold deposit of the Gurupi Belt, northern Brazil, belongs to the class of orogenic gold deposits as mentioned in this paper, and is hosted in highly strained graphitic schist belonging to a Paleoproterozoic metavolcano-sedimentary sequence.
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Fluid systems and fracture development during syn-depositional fold growth: An example from the Pico del Aguila anticline, Sierras Exteriores, southern Pyrenees, Spain

TL;DR: In this article, an integrated, spatio-temporal analysis of the fracture-controlled paleo-fluid system in the Pico del Aguila anticline, a N-S trending fold located in the southern front of the Spanish Pyrenees, is presented.
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Dolomitization of Lower Cretaceous Peritidal Carbonates By Modified Seawater: Constraints From Clumped Isotopic Paleothermometry, Elemental Chemistry, and Strontium Isotopes

TL;DR: In this paper, the authors investigated one of the few examples of dolomitization of Lower Cretaceous shallow-water limestones from the southern Tethys carbonate platform from outcrops on the Haushi-Huqf High in central-east Oman.
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The Anatomy of an Early Dinantian Terraced Floodplain: Palaeo‐Environment and Early Diagenesis

TL;DR: In this paper, the lowermost Carboniferous rocks in the Cockburnspath area of east Berwickshire (southern Scotland) are interpreted as coastal floodplain sediments.
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Early and late Neoproterozoic C, O and Sr isotope chemostratigraphy in the carbonates of West Congo and Mbuji-Mayi supergroups: A preserved marine signature?

TL;DR: In this article, the fidelity of δ13Ccarb and Sr signatures in Neoproterozoic carbonates was discussed on the basis of a severe diagenetic control, using trace and major geochemistry, combined with C and O stable isotope analysis, highlighting that the δ 13Ccarb fluctuations of the Schisto-Calcaire Subgroup reflect (i) facies variations, (ii) exchanges between isotopically light carbon in meteoric waters and carbonate during lithification and early diagenesis, and/or (iii) regional metamorph
References
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Journal ArticleDOI

Isotopic standards for carbon and oxygen and correction factors for mass-spectrometric analysis of carbon dioxide

TL;DR: In this paper, Niee's and Solenhofen standards were compared to the Chicago PDB standard for carbon and oxygen isotope ratios, and the correction factors for instrumental effects and for the nature of the mass spectra were derived.
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On the Isotopic Chemistry of Carbonates and a Paleotemperature Scale

TL;DR: In this paper, the temperature variation of the fractionation of oxygen in exchange reactions between dissolved carbonate and water and between calcite and water was calculated on theoretical grounds, and checked experimentally.
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The use of bromine pentafluoride in the extraction of oxygen from oxides and silicates for isotopic analysis

TL;DR: In this paper, a technique was developed in which bromine pentafluoride was used as a reagent for quantitative liberation of oxygen from oxides and silicates, and the results of isotopic analyses were compared with measurements made in other laboratories by other procedures.
Journal ArticleDOI

Measurement of O18O16 ratios of total oxygen of carbonates

TL;DR: The commonly used phosphoric acid procedure for the determination of oxygen isotope abundances in carbonates involves a large kinetic isotope effect as mentioned in this paper, which leads to an overestimate of the dolomite-calcite oxygon isotope fractionation by 0.8 per mil.
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