Nielsen, Sune G. et al. (2011): Thallium isotopes in early diagenetic pyrite; a paleoredox proxy?

Leg/Site/Hole:
ODP 165
ODP 167
Identifier:
2012-005329
georefid

10.1016/j.gca.2011.07.047
doi

Creator:
Nielsen, Sune G.
University of Oxford, Department of Earth Sciences, Oxford, United Kingdom
author

Goff, Matt
Georgia Institute of Technology, United States
author

Hesselbo, Stechen P.
Rice University, United States
author

Jenkyns, Hugh C.
author

LaRowe, Doug E.
author

Lee, Cin-Ty A.
author

Identification:
Thallium isotopes in early diagenetic pyrite; a paleoredox proxy?
2011
Geochimica et Cosmochimica Acta
Elsevier, New York, NY, International
75
21
6690-6704
This paper presents the first study of Tl isotopes in early diagenetic pyrite. Measurements from two sections deposited during the Toarcian Ocean Anoxic Event (T-OAE, approximately 183Ma) are compared with data from late Neogene (<10Ma) pyrite samples from ODP legs 165 and 167 that were deposited in relatively oxic marine environments. The Tl isotope compositions of late Neogene pyrites are all significantly heavier than seawater, which most likely indicates that Tl in diagenetic pyrite is partially sourced from ferromanganese oxy-hydroxides that are known to display relatively heavy Tl isotope signatures. One of the T-OAE sections from Peniche in Portugal displays pyrite thallium isotope compositions indistinguishable from late Neogene samples, whereas samples from Yorkshire in the UK are depleted in the heavy isotope of Tl. These lighter compositions are best explained by the lack of ferromanganese precipitation at the sediment-water interface due to the sulfidic (euxinic) conditions thought to be prevalent in the Cleveland Basin where the Yorkshire section was deposited. The heavier signatures in the Peniche samples appear to result from an oxic water column that enabled precipitation of ferromanganese oxy-hydroxides at the sediment-water interface. The Tl isotope profile from Yorkshire is also compared with previously published molybdenum isotope ratios determined on the same sedimentary succession. There is a suggestion of an anti-correlation between these two isotope systems, which is consistent with the expected isotope shifts that occur in seawater when marine oxic (ferromanganese minerals) fluxes fluctuate. The results outlined here represent the first evidence that Tl isotopes in early diagenetic pyrite have potential to reveal variations in past ocean oxygenation on a local scale and potentially also for global oceans. However, much more information about Tl isotopes in different marine environments, especially in anoxic/euxinic basins, is needed before Tl isotopes can be confidently utilized as a paleo-redox tracer. Abstract Copyright (2011) Elsevier, B.V.
English
Serial
Coverage:Geographic coordinates:
North:42.0000
West:-128.0000East: -65.0000
South:10.3000

Isotope geochemistry; Stratigraphy; Atlantic Ocean; Caribbean Sea; Cenozoic; chemical composition; Cleveland Basin; crystal chemistry; diagenesis; East Pacific; Eh; England; Europe; geochemistry; Great Britain; Iberian Peninsula; ICP mass spectra; isotopes; Jurassic; Leg 165; Leg 167; Lower Jurassic; major elements; mass spectra; Mesozoic; metals; Neogene; North Atlantic; North Pacific; Northeast Pacific; Ocean Drilling Program; oceanic anoxic events; Pacific Ocean; paleo-oceanography; paleoenvironment; Peniche Portugal; Pliocene; Portugal; pyrite; sea water; Southern Europe; spectra; sulfides; Tertiary; thallium; Toarcian; trace elements; United Kingdom; upper Liassic; Western Europe; Yorkshire England;

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