T217 Deciphering the Major Paleoenvironmental Crises of the Earth and Their Impact on the Marine Ecosystems and Biogeochemical Cycles
Tuesday, 24 October 2017
8:00 AM - 12:00 PM
Room 307/308
RAPID CHANGES IN MAJOR ION CHEMISTRY OF SEAWATER AND THE END-PERMIAN MASS EXTINCTION
Paper number: T217-6
Program: Technical Sessions
Time: 9:15 AM – 9:35 AM
Authors
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Javier Garcia VeigasUniversity of Barcelona, Barcelona
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Dioni I. CendónKirrawee DC
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Lluís Gibert BeotasUniversitat de Barcelona, Barcelona, N/A
Abstract
Permian seawater, determined from the chemical compositions of fluid inclusions in marine halites from the North American Permian Basin (Kansas, Texas and New Mexico) and the Southern Permian Basin (Central Europe) shares chemical characteristics with modern seawater, including SO4 > Ca at the point of gypsum precipitation and evolution into a Mg-Na-K-SO4-Cl brine. An abrupt shift to Ca-rich fluid inclusions occurs in the Changhsingian Rustler Formation of New Mexico over 1.5 meter of stratigraphic section and in the Changhsingian Zechstein Cycle Na2 and basal Na3 Cycle of Poland. Such an abrupt shift in the major ion chemistry of seawater in two basins at about the same time is unusual because the residence times of SO4 and Ca in seawater are 10 m.y. and 1 m.y., respectively. Changes in the major ion chemistry of seawater are well known to occur over periods of 106 to 107 years, so the end-Permian seawater chemistry shift indicates some catastrophic process. The shift from sulfate-rich to calcium-rich brines coincides with a marked drop in δ34S in Zechstein and Rustler anhydrite, which suggests a link between changes in the major ion chemistry of seawater and perturbations in the sulfur cycle. These changes are interpreted to have been caused by overturn of anoxic sulfidic deep-waters from the Panthalassan superocean during the Changhsingian stage which may have coincided with the end-Permian mass extinction.
Geological Society of America Abstracts with Programs. Vol. 49, No. 6
doi: 10.1130/abs/2017AM-299971
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