Ferruginous Conditions Dominated Later Neoproterozoic Deep-Water Chemistry

Author:

Canfield Donald E.12345,Poulton Simon W.12345,Knoll Andrew H.12345,Narbonne Guy M.12345,Ross Gerry12345,Goldberg Tatiana12345,Strauss Harald12345

Affiliation:

1. Nordic Center for Earth Evolution and Institute of Biology, Campusvej 55, University of Southern Denmark, 5230 Odense, Denmark.

2. School of Civil Engineering and Geosciences, Newcastle University, Drummond Building, Newcastle upon Tyne NE1 7RU, UK.

3. Botanical Museum, Harvard University, Cambridge, MA 02138, USA.

4. Department of Geological Sciences and Geological Engineering, Queen's University, Kingston, Ontario K7L 3N6, Canada.

5. Kupa'a Farm, Post Office Box 458, Kula, HI96790, USA.

Abstract

Earth's surface chemical environment has evolved from an early anoxic condition to the oxic state we have today. Transitional between an earlier Proterozoic world with widespread deep-water anoxia and a Phanerozoic world with large oxygen-utilizing animals, the Neoproterozoic Era [1000 to 542 million years ago (Ma)] plays a key role in this history. The details of Neoproterozoic Earth surface oxygenation, however, remain unclear. We report that through much of the later Neoproterozoic (<742 ± 6 Ma), anoxia remained widespread beneath the mixed layer of the oceans; deeper water masses were sometimes sulfidic but were mainly Fe 2+ -enriched. These ferruginous conditions marked a return to ocean chemistry not seen for more than one billion years of Earth history.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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