Showing papers by "Geoff Nowell published in 2017"

The behavior of iron and zinc stable isotopes accompanying the subduction of mafic oceanic crust: A case study from Western Alpine ophiolites

Abstract: Arc lavas display elevated Fe3+/ΣFe ratios relative to MORB. One mechanism to explain this is the mobilization and transfer of oxidized or oxidizing components from the subducting slab to the mantle wedge. Here we use iron and zinc isotopes, which are fractionated upon complexation by sulfide, chloride, and carbonate ligands, to remark on the chemistry and oxidation state of fluids released during prograde metamorphism of subducted oceanic crust. We present data for metagabbros and metabasalts from the Chenaillet massif, Queyras complex, and the Zermatt-Saas ophiolite (Western European Alps), which have been metamorphosed at typical subduction zone P-T conditions and preserve their prograde metamorphic history. There is no systematic, detectable fractionation of either Fe or Zn isotopes across metamorphic facies, rather the isotope composition of the eclogites overlaps with published data for MORB. The lack of resolvable Fe isotope fractionation with increasing prograde metamorphism likely reflects the mass balance of the system, and in this scenario Fe mobility is not traceable with Fe isotopes. Given that Zn isotopes are fractionated by S-bearing and C-bearing fluids, this suggests that relatively small amounts of Zn are mobilized from the mafic lithologies in within these types of dehydration fluids. Conversely, metagabbros from the Queyras that are in proximity to metasediments display a significant Fe isotope fractionation. The covariation of δ56Fe of these samples with selected fluid mobile elements suggests the infiltration of sediment derived fluids with an isotopically light signature during subduction.

High precision osmium stable isotope measurements by double spike MC-ICP-MS and N-TIMS

Abstract: Osmium stable isotopes provide a new, potentially powerful tool with which to investigate a diverse range of geological processes including planetary formation, ore-genesis and weathering. In this paper, we present a new technique for high precision measurement of osmium (Os) stable isotope ratios by both Multiple-Collector Inductively Coupled Plasma Mass Spectrometry (MC-ICP-MS) and Negative ion Thermal Ionisation Mass Spectrometry (N-TIMS). We use a 188Os–190Os double spike, composed of 61% 188Os and 39% 190Os, to correct for mass dependent fractionation resulting from sample preparation and isotope measurement, with the ideal spike to sample ratio being 55 : 45. Isotope ratios are expressed as δ190Os which is the per mil deviation in the measured 190Os/188Os ratio relative to isotope reference material DROsS. Repeated analyses of double spiked DROsS for both MC-ICP-MS (n = 80 cycles) and N-TIMS (n = 280 cycles) show that an internal precision of 0.01–0.02‰ on δ190Os (2 se) can be attained, with a long-term reproducibility of 0.016‰ and 0.029‰ (2 sd; n = 91 and 83, respectively). The better reproducibility on MC-ICP-MS than on N-TIMS is, predominantly, due to measurement at higher beam intensities (11–18 V with consumption of ∼200 ng natural Os vs. 2–18 V with consumption of 2.3–45 ng natural Os, respectively). In addition to stable isotope compositions, our method allows for simultaneous measurement of 187Os/188Os and 186Os/188Os ratios with a precision of <40 ppm (2 se; 80 cycles for MC-ICP-MS and 280 cycles for N-TIMS) and an external reproducibility of 123–268 ppm and 234–361 ppm (2 sd; n = 91 for MC-ICP-MS and n = 83 for N-TIMS), respectively. We demonstrate that a similar precision and reproducibility can be obtained for other pure Os solutions as well as for geological materials. Furthermore, with a range of of analytical tests we evaluate and demonstrate the robustness of our method with regards to residual matrix effects and interference correction, signal intensity and on-peak zero on MC-ICP-MS, and the effect of oxygen corrections and isobaric interference on N-TIMS. Finally, we report the first Os stable isotope compositions for geological reference materials, including mantle peridotites and chromitites, and one ordinary chondrite.