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Journal article

Molybdenum isotopic composition of modern and Carboniferous carbonates

  • Voegelin, Andrea R. Institut für Geologie, Universität Bern, Switzerland
  • Nägler, Thomas F. Institut für Geologie, Universität Bern, Switzerland
  • Samankassou, Elias Département de Géosciences, Géologie et Paléontologie, Université de Fribourg, Switzerland - Department of Sedimentology and Marine Geology, FALW, VU University Amsterdam, The Netherlands - Département de Géologie et Paléontologie, Université de Genève, Switzerland
  • Villa, Igor M. Institut für Geologie, Universität Bern, Switzerland - Dipartimento di Scienze Geologiche e Geotecnologie, Università di Milano, Italy
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    21.05.2009
Published in:
  • Chemical Geology. - 2009, vol. 265, no. 3-4, p. 488-498
molybdenum isotopes
carbonates
heavy stable isotopes
paleo-oceanography
English We investigate the redox-sensitive isotope system of molybdenum (Mo) in marine carbonates to evaluate their potential as archive of the Mo isotopic composition of coeval seawater. We present Mo isotope data (δ98/95Mo) of modern skeletal and non-skeletal carbonates as well as a variety of precipitates from the mid and late Carboniferous. The external reproducibility is determined by repeated analyses of two commercially available carbonate standards. The resulting uncertainty of the low concentration samples is ± 0.1‰ (2σ). Analysis of modern ooid sands from the Bahamas shows a consistently heavy Mo isotopic composition (δ98/95Mo between 2 and 2.2‰), approaching modern mean seawater values (δ98/95Mo = 2.3‰ ± 0.1‰ (2σ)). This suggests that isotope fractionation during Mo uptake into non-skeletal carbonate precipitates is small. In contrast, modern skeletal carbonates show variable isotopic compositions (0.1 to 2.2‰) which suggests a biologically controlled fractionation process. The varying Mo signatures found in Carboniferous cement phases point to a strong response to local changes in fluid composition from which they precipitated. Overall, we recognized three important factors to cause an offset relative to ocean water: Mo derived from skeletal components, input of detrital Mo and admixture of light, hydroxide derived Mo via diagenetic fluids. All of these factors cause a lighter Mo isotopic composition relative to seawater. Due to the apparent small isotope fractionation during Mo uptake into non-skeletal carbonates, their δ98/95Mo closely reflects the ambient fluid composition. From these results we conclude that carbonates represent a promising new tool to characterize the water mass Mo isotopic composition of marine paleo-environments.
Faculty
Faculté des sciences et de médecine
Department
Département de Géosciences
Language
  • English
Classification
Palaeontology
License
License undefined
Identifiers
Persistent URL
https://folia.unifr.ch/unifr/documents/301239
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