4.7 Article

Onset of oxidative weathering of continents recorded in the geochemistry of ancient glacial diamictites

Journal

EARTH AND PLANETARY SCIENCE LETTERS
Volume 408, Issue -, Pages 87-99

Publisher

ELSEVIER
DOI: 10.1016/j.epsl.2014.10.002

Keywords

glaciation; oxygen; Precambrian; Great Oxidation Event; diamictite; upper continental crust

Funding

  1. NSF [EAR-1321954, FESD EAR-1338810]
  2. State Key Laboratory of Geological Processes
  3. Mineral Resources at China University of Geosciences in Wuhan
  4. Division Of Earth Sciences
  5. Directorate For Geosciences [1321954, 1338810] Funding Source: National Science Foundation

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Glacial diamictites deposited in the Mesoarchean, Paleoproterozoic, Neoproterozoic, and Paleozoic eras record temporal variations in their average compositions that reflect the changing composition of the upper continental crust (UCC). Twenty six of the 27 units studied show elevated chemical index of alternation (CIA) and low Sr abundances, regardless of their age, documenting pervasive weathering of the average UCC. Lower abundances of transition metals reflect a shift towards more felsic crustal compositions after the Archean. Superimposed on this chemical difference is the signal of the rise of oxidative weathering of the continents, recorded by changes in the absolute and relative abundances of the redox sensitive elements Mo and V. Neoproterozoic and Paleozoic diamictites show pervasive depletion in Mo and V, reflecting their loss from the continents due to increasing intensity of oxidative weathering, as also recorded in some of the Paleoproterozoic diamictites. A few of the Paleoproterozoic diamictites deposited after the Great Oxidation Event show no depletion in Mo and V (e.g., Gowganda), but such signatures could be inherited from their provenance. In contrast, the pre-GOE Duitschland diamictite (ca. 2.3-2.5 Ga) from South Africa reveals evidence of intense oxidative weathering (i.e., large depletions in Mo), supporting a growing body of observations showing the presence of measurable atmospheric oxygen prior to permanent loss of the mass independent fractionation signal in sulfur isotopes. (C) 2014 Elsevier B.V. All rights reserved.

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