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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
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    Unknown
    PANGAEA
    In:  Supplement to: Rasoazanamparany, Christine; Widom, Elisabeth; Siebe, Claus; Guilbaud, M N; Spicuzza, Michael J; Valley, John W; Valdez, G; Salinas, S (2016): Temporal and compositional evolution of Jorullo volcano, Mexico: Implications for magmatic processes associated with a monogenetic eruption. Chemical Geology, 434, 62-80, https://doi.org/10.1016/j.chemgeo.2016.04.004
    Publication Date: 2023-01-13
    Description: The 1759-1774 eruption of the Jorullo volcano in the Michoacán Guanajuato Volcanic Field (MGVF), Mexico, produced lavas that range in composition from basalt to basaltic andesite. We have conducted new major and trace element and isotopic studies (whole rock Sr-Nd-Pb-Hf-Os, and O isotopes in olivine separates) of the Jorullo lavas and tephras spanning the duration and compositional range of the eruption, to further constrain the potential roles of mantle source heterogeneity, subduction-related metasomatism, and crustal assimilation in the petrogenesis of the Jorullo magmas. This study presents the first Hf, high precision Pb and comprehensive oxygen isotope measurements for Jorullo volcanic rocks. All samples have arc-like trace element patterns with enrichments in large ion lithophile elements (e.g. Ba, Rb, and Pb) and depletions in fluid immobile elements (e.g. Nb, Ta). In addition, the samples show variations in 87Sr/86Sr (0.7038-0.7040), 143Nd/144Nd (0.51280-0.51285), 176Hf/177Hf (0.28297-0.28300), 206Pb/204Pb (18.62-18.66), 207Pb/204Pb (15.57-15.59) and 208Pb/204Pb (38.34-38.43). Osmium isotope signatures are, with one exception, more radiogenic than the depleted and primitive mantle (187Os/188Os = 0.1231-0.1616). Oxygen isotope ratios of olivine phenocrysts (d18.OSMOW = 5.70-6.02 per mil) show limited variation, but are isotopically heavier than normal mantle olivine. The samples define two geochemical groups: high-MgO samples with higher 87Sr/86Sr, lower 143Nd/144Nd and 176Hf/177Hf, and a positive correlation of Sr and Pb isotopes; and low-MgO samples displaying lower 87Sr/86Sr but higher 143Nd/144Nd and 176Hf/177Hf than the former group, and a negative correlation of Sr and Pb isotopes. The high-MgO group comprises most of the early tephra and lavas, whereas the low-MgO group includes most of the late tephra and lavas. These compositional variations are inconsistent with shallow level contamination, but rather are interpreted to reflect mantle source heterogeneity. Trace element and isotopic signatures are consistent with North Mexican Extensional Province (NMEP) mantle metasomatised by subduction components composed of sediment- and oceanic crust-derived hydrous fluid. The temporal-compositional variations observed in Jorullo magmas are inferred to result from a combination of variable degrees of fractional crystallization of magmas produced by tapping a progressively less metasomatised mantle source that is vertically and/or laterally heterogeneous.
    Type: Dataset
    Format: application/zip, 3 datasets
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  • 3
    Publication Date: 2023-01-13
    Keywords: -; Aluminium oxide; Calcium oxide; Chromium(III) oxide; Event label; Forsterite; Iron oxide, Fe2O3; Iron oxide, FeO; JOR-0609B; JOR-0721; JOR-0722; JOR-0733; JOR-0759; JOR-0760; JOR-0766; JOR-0766A; JOR-0766B; Magnesium oxide; Manganese oxide; Mexico; Microprobe; Nickel oxide; Sample comment; Sample ID; Silicon dioxide; Titanium dioxide; Total
    Type: Dataset
    Format: text/tab-separated-values, 2160 data points
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  • 4
    Publication Date: 2023-07-10
    Keywords: Aluminium oxide; Antimony; Barium; Caesium; Calcium oxide; Cerium; Chromium; Cobalt; Copper; Dysprosium; Erbium; Europium; Event label; Gadolinium; Gallium; Hafnium; Holmium; Iron oxide, FeO; JOR-0603A; JOR-0603B; JOR-0604A; JOR-0605; JOR-0606; JOR-0608; JOR-0610; JOR-0723; JOR-0731; JOR-0734; JOR-0736; JOR-0737; JOR-0764; JOR-0765; JOR-0766; JOR-0770; JOR-0880; JOR-0894; Lanthanum; Lead; Lutetium; Magnesium oxide; Manganese oxide; Mexico; Molybdenum; Neodymium; Nickel; Niobium; Phosphorus pentoxide; Potassium oxide; Praseodymium; Rubidium; Samarium; Sample comment; Scandium; Silicon dioxide; Sodium oxide; Strontium; Tantalum; Terbium; Thorium; Thulium; Titanium dioxide; Total; Tungsten; Uranium; Vanadium; Ytterbium; Yttrium; Zinc; Zirconium
    Type: Dataset
    Format: text/tab-separated-values, 837 data points
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  • 5
    Publication Date: 2023-07-10
    Keywords: -; Aluminium oxide; Barium; Caesium; Calcium oxide; Cerium; Chromium; Comment; Copper; Dysprosium; Erbium; Europium; Event label; Gadolinium; Gallium; Hafnium; Hafnium-176/Hafnium-177; Holmium; Iron oxide, FeO; JOR-0603A; JOR-0603A1; JOR-0603A2; JOR-0603A3; JOR-0603A4; JOR-0603B; JOR-0603C; JOR-0603D; JOR-0603E; JOR-0603F; JOR-0603G; JOR-0609B; JOR-0611; JOR-0712; JOR-0719; JOR-0721; JOR-0722; JOR-0726; JOR-0726r; JOR-0730; JOR-0733; JOR-0753; JOR-0759; JOR-0760; JOR-0763; JOR-0766; JOR-1290C; JOR-1290D; JOR-1290E; Lanthanum; Lead; Lead-206/Lead-204 ratio; Lead-207/Lead-204 ratio; Lead-208/Lead-204 ratio; Lutetium; Magnesium oxide; Manganese oxide; MC-ICPM; Mexico; Neodymium; Neodymium-143/Neodymium-144 ratio; Nickel; Niobium; Osmium-187/Osmium-188 ratio; Phosphorus pentoxide; Potassium oxide; Praseodymium; Ratio; Rubidium; Samarium; Sample type; Scandium; Silicon dioxide; Sodium oxide; Strontium; Strontium-87/Strontium-86 ratio; Tantalum; Terbium; Thermal Ionization Mass Spectrometry (TIMS); Thorium; Thulium; Titanium dioxide; Total; Uranium; Vanillin; X-ray fluorescence (XRF); Ytterbium; Yttrium; Zinc; Zirconium; δ18O
    Type: Dataset
    Format: text/tab-separated-values, 1649 data points
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  • 6
    Publication Date: 2021-06-30
    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: Key Points: Three widely available tourmaline reference materials are characterized for δ7Li, δ17O and δ18O, while new EPMA and SIMS measurements refine their major element compositions. SIMS data document homogeneity for these isotope ratios. SIMS matrix effect causes bias of 1.9‰ between elbaite and schorl, whereas silicate glass shows even more severe bias.
    Description: U.S. National Science Foundation
    Description: Natural Environment Research Council http://dx.doi.org/10.13039/501100000270
    Description: US Department of Energy http://dx.doi.org/10.13039/100000015
    Keywords: 551.9 ; tourmaline ; lithium isotopes ; oxygen isotopes ; reference materials ; SIMS ; matrix effect
    Type: article
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  • 7
    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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