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Published June 1992 | public
Journal Article

Geochemistry of Precambrian carbonates: V. Late Paleoproterozoic seawater

Abstract

In an effort to obtain better constrained data for the first- and second-order variations in the isotopic composition of late Paleoproterozoic (1.8 ± 0.2 Ga) seawater, we report a study of mineralogy, chemistry, and isotopic composition of the Coronation Supergroup (~1.9 Ga, NWT), Canada, and the McArthur Group (~1.65 Ga, NT), Australia. Petrologically, both carbonate sequences are mostly dolostones. The McArthur population, however, contains more abundant textural features that attest to the former presence of sulfates and halite, and the facies investigated herein probably represent ancient equivalents of modern evaporitic sabkhas and lacustrine playa lakes. This is reflected in ^(18)O enrichment (up to −2.9%. PDB) and high Mn, Fe, and Sr concentrations. Nonetheless, the available Δ^(18)O data indicate that the "best estimate" for the Archean to late Paleoproterozoic limestones is about −7%. PDB, with dolostones some 3 ± 2%. heavier. The observed Δ^(18)O_doiomitc-calcite is thus within the range of the proposed fractionation factor for a cogenetic mineral pair. This, together with the consistency of isotopic patterns for sedimentological facies over almost 2 billion years, from the late Paleoproterozoic to the present, suggest that dolomitization was an early diagenetic event and that the ^(18)O depletion of the Archean to late Paleoproterozoic carbonates is not an artefact ofpost-depositional alteration. The δ^(13)C, although within the range of other Precambrian and Phanerozoic carbonates, indicates a possible secular evolution from 0 ± 2%. PDB at 1.9 Ga ago to −1 ± 1.5%. at 1.65 Ga ago. The secular evolution for reflects the ^(87)Sr increase from 0.7031 ± 0.0008 at 3.5 ± 0.1 Ga ago, through 0.7025 ± 0.0015 at 2.8 ± 0.2 Ga, 0.7033 at 2.5 Ga, 0.7050 at 2.25 ± 0.25 Ga, 0.7047 at 1.91, to ≤0.706 at 1.65 Ga ago.

Additional Information

© 1992 Pergamon Press Ltd. Received May 10, 1991; accepted in revised form March 25, 1992. This work has been supported financially by the NSF (Grant No. EAR-831 3579 to Jan Veizer, R. N. Clayton, and Abraham Lerman at the time of Veizer's stay at the Department of Geological Sciences, Northwestern University, Evanston, Illinois) and in the final stages by the Natural Sciences and Engineering Research Council of Canada and Canada Council (Killam Research Fellowship to JV). R. W. Hinton acknowledges the support by NASA (grant NAG 9-5 1 to RNC). K. Bell and J. Blenkinsop provided access to solid source mass spectrometer, J. M. Oly carried out isotope analysis for K. A. Plumb in the Bureau of Mineral Resources stable isotope laboratory. We acknowledge technical support of W. Schmiedel and A. Sodonis, typing of the manuscript by B. Kemper, drafting of figures by W. Malcherek, photography by M. Ress, provision of samples by the Northern Territory Geological Survey and logistic advice by N. Williams. K. A. Plumb publishes with the permission of the Director, Bureau of Mineral Resources, Geology and Geophysics. Constructive reviews of D. R. Lowe, B. E. Taylor, D. F. Williams, S.-S. Sun, and an anonymous reviewer have been appreciated.

Additional details

Created:
August 22, 2023
Modified:
October 17, 2023