Sulfidic anoxia in the oceans during the Late Ordovician mass extinctions – insights from molybdenum and uranium isotopic global redox proxies

Tais W. Dahl*, Emma U. Hammarlund, Christian Mac Ørum Rasmussen, David P. G. Bond, Donald E. Canfield

*Corresponding author af dette arbejde

Publikation: Bidrag til tidsskriftReviewForskningpeer review

34 Citationer (Scopus)
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Abstract

The Late Ordovician Mass Extinction wiped out 85% of animal species in two phases (LOME1 and LOME2). The kill mechanisms for the extinction phases are debated, but deteriorating climate and the expansion of marine anoxia appear to have been important factors. Nevertheless, the spatial extent and intensity of marine anoxia and its temporal relationship with the extinctions are not well understood. Here, we review existing global paleoredox proxy data based on molybdenum (Mo) and uranium (U) isotopes from four paleocontinents combined with new Mo isotope data from Dob's Linn, Scotland. Individually, these sedimentary records demonstrate significant redox fluctuations, but our coupled dynamic oceanic mass balance model for the evolution of the marine Mo and U cycles reveals that globally expansive ocean anoxia is best constrained by δ238U in carbonates from Anticosti Island that record expansive anoxia during LOME2. In addition, we consider periodic sulfidic anoxia developing in well-ventilated parts of the shallow oceans (e.g. during warmer periods with greater solar insolation) to have produced temporarily high seawater δ98Mo values during LOME1 in accordance with trends to high values observed in the sedimentary records. In this view, oceanic oxygen loss had a causal role during both extinction phases in the Late Ordovician.

OriginalsprogEngelsk
Artikelnummer103748
TidsskriftEarth-Science Reviews
Vol/bind220
Antal sider14
ISSN0012-8252
DOI
StatusUdgivet - 2021

Bibliografisk note

Funding Information:
The authors thank Ariel Anbar, Gwyneth Gordon, and Stephen Romaniello from Arizona State University who assisted with mass spectrometric analyses at the W. M. Keck laboratory for Environmental Biogeochemistry. TWD thanks the Carlsberg Foundation (CF16-0876) and the Danish Council for Independent Research (DFF - 7014-00295, DFF-8102-00005B) for financial support. EUH thanks the Swedish Research Council (Grant 04693). CM?R is grateful for funding received through GeoCenter Denmark (Grants 2015-5 and 3-2017). DC thanks the Villum Foundation (Villum Grant 16518) for financial support.

Funding Information:
The authors thank Ariel Anbar, Gwyneth Gordon, and Stephen Romaniello from Arizona State University who assisted with mass spectrometric analyses at the W. M. Keck laboratory for Environmental Biogeochemistry. TWD thanks the Carlsberg Foundation ( CF16-0876 ) and the Danish Council for Independent Research ( DFF - 7014-00295, DFF-8102-00005B ) for financial support. EUH thanks the Swedish Research Council (Grant 04693 ). CMØR is grateful for funding received through GeoCenter Denmark (Grants 2015-5 and 3-2017 ). DC thanks the Villum Foundation (Villum Grant 16518 ) for financial support.

Publisher Copyright:
© 2021

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