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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 133 (1998), S. 1-11 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The oxygen isotope ratios of Phanerozoic zircons from kimberlite pipes in the Kaapvaal Craton of southern Africa and the Siberian Platform vary from 4.7 to 5.9‰ VSMOW. High precision, accurate analyses by laser reveal subtle pipe-to-pipe differences not previously suspected. These zircons have distinctive chemical and physical characteristics identifying them as mantle-derived megacrysts similar to zircons found associated with diamond, coesite, MARID xenoliths, Cr-diopside, K-richterite, or Mg-rich ilmenite. Several lines of evidence indicate that these 18O values are unaltered by kimberlite magmas during eruption and represent compositions preserved since crystallization in the mantle, including: U/Pb age, large crystal size, and the slow rate of oxygen exchange in non-metamict zircon. The average 18O of mantle zircons is 5.3‰, ∼0.1 higher and in equilibrium with values for olivine in peridotite xenoliths and oceanic basalts. Zircon megacrysts from within 250 km of Kimberley, South Africa have average 18O=5.32±0.17 (n=28). Small, but significant, differences among other kimberlite pipes or groups of pipes may indicate isotopically distinct reservoirs in the sub-continental lithosphere or asthenosphere, some of which are anomalous with respect to normal mantle values of 5.3±0.3. Precambrian zircons (2.1–2.7 Ga) from Jwaneng, Botswana have the lowest values yet measured in a mantle zircon, 18O=3.4 to 4.7‰. These zircon megacrysts originally crystallized in mafic or ultramafic rocks either through melting and metasomatism associated with kimberlite magmatism or during metamorphism. The low 18O zircons are best explained by subduction of late Archean ocean crust that exchanged with heated seawater prior to underplating as eclogite and to associated metasomatism of the mantle wedge. Smaller differences among other pipes and districts may result from variable temperatures of equilibration, mafic versus ultramafic hosts, or variable underplating. The narrow range in zircon compositions found in most pipes suggests magmatic homogenization. If this is correct, these zircons document the existence of significant quantities of magma in the sub-continental mantle that was regionally variable in 18O and this information restricts theories about the nature of ancient subduction.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2022-10-26
    Description: © The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Wiedenbeck, M., Trumbull, R. B., Rosner, M., Boyce, A., Fournelle, J. H., Franchi, I. A., Halama, R., Harris, C., Lacey, J. H., Marschall, H., Meixner, A., Pack, A., von Strandmann, P. A. E. P., Spicuzza, M. J., Valley, J. W., & Wilke, F. D. H. Tourmaline reference materials for the In situ analysis of oxygen and lithium isotope ratio compositions. Geostandards and Geoanalytical Research, (2020), doi:10.1111/ggr.12362.
    Description: Three tourmaline reference materials sourced from the Harvard Mineralogical and Geological Museum (schorl 112566, dravite 108796 and elbaite 98144), which are already widely used for the calibration of in situ boron isotope measurements, are characterised here for their oxygen and lithium isotope compositions. Homogeneity tests by secondary ion mass spectrometry (SIMS) showed that at sub‐nanogram test portion masses, their 18O/16O and 7Li/6Li isotope ratios are constant within ± 0.27‰ and ± 2.2‰ (1s), respectively. The lithium mass fractions of the three materials vary over three orders of magnitude. SIMS homogeneity tests showed variations in 7Li/28Si between 8% and 14% (1s), which provides a measure of the heterogeneity of the Li contents in these three materials. Here, we provide recommended values for δ18O, Δ’17O and δ7Li for the three Harvard tourmaline reference materials based on results from bulk mineral analyses from multiple, independent laboratories using laser‐ and stepwise fluorination gas mass spectrometry (for O), and solution multi‐collector inductively coupled plasma‐mass spectroscopy (for Li). These bulk data also allow us to assess the degree of inter‐laboratory bias that might be present in such data sets. This work also re‐evaluates the major element chemical composition of the materials by electron probe microanalysis and investigates these presence of a chemical matrix effect on SIMS instrumental mass fractionation with regard to δ18O determinations, which was found to be 〈 1.6‰ between these three materials. The final table presented here provides a summary of the isotope ratio values that we have determined for these three materials. Depending on their starting mass, either 128 or 512 splits have been produced of each material, assuring their availability for many years into the future.
    Description: JWV and MJS (University of Wisconsin) are supported by the U.S. National Science Foundation (EAR‐1524336) and Department of Energy (DE‐FG02‐93‐ER14389). MR acknowledges the use of the NSF‐supported WHOI ICP‐MS facility and thanks Larry Ball and Jerzy Blusztajn for their assistance. Analyses at Bristol were supported by NERC grant NER/C510983/1. Finally, we wish to thank the Harvard Museum for ongoing support of such projects. Open access funding enabled and organized by ProjektDEAL.
    Keywords: Tourmaline ; Lithium isotopes ; Oxygen isotopes ; Reference materials ; SIMS ; Matrix effect
    Repository Name: Woods Hole Open Access Server
    Type: Article
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