T233 Apatite, from Magma to Medicine: In Honor of John M. Hughes
Wednesday, 7 November 2018
8:00 AM - 12:00 PM
Room 242
A NEW EU VALENCE CALIBRATION FOR APATITE IN BASALTIC SYSTEM: AN EXPERIMENTAL STUDY COMBINING XANES, EU/EU* AND LATTICE STRAIN
Paper number: T233-11
Program: Technical Sessions
Time: 10:25 AM – 10:40 AM
Authors
-
Dustin TrailUniversity of Rochester, Rochester, NY
-
E. Bruce WatsonRensselaer Polytechnic Institute, Troy, NY
Abstract
(i) a XANES calibration that directly measures Eu valence species in apatite (i.e., Eu2+ and Eu3+) in basalts that crystallize between 1175-1100 °C.
(ii) a technique that involves measurement of Sm, Eu and Gd in co-existing apatite and basalt, such that the intensity of the negative Eu anomaly is monitored by (Eu/√(SmxGd))
(iii) a technique based on the negative Eu excursion from the lattice strain model defined by REE3+ between apatite and basalt.
From an application perspective it is worth noting that Eu valence partitioning techniques based on (√SmxGd) and lattice strain are indistinguishable. Application of these three calibrations is best carried out in systems where both apatite and co-existing glass are present and in direct contact. In crystalline rocks (i.e., where co-existing glass cannot be analyzed), whole rock analyses can be used as a guide but considerations/corrections must be made to ensure that the effect of plagioclase crystallization can be removed. Similarly, if the melt source has an inherited negative Eu anomaly, appropriate corrections must also be made. In addition to the reported redox calibrations, the partition coefficients for REE range from a maximum DEu3+= 1.67 ±v 0.25 (as determined by lattice strain) to DEu2+ = 0.69 ± 0.10. These partition coefficient values, as observed in the Onuma diagram, show apatite is in a fortuitous situation were the most compatible REE (Eu3+) is also the polyvalent element used to monitor fO2.
Geological Society of America Abstracts with Programs. Vol. 50, No. 6
doi: 10.1130/abs/2018AM-323095
© Copyright 2018 The Geological Society of America (GSA), all rights reserved. Permission is hereby granted to the author(s) of this abstract to reproduce and distribute it freely, for noncommercial purposes. Permission is hereby granted to any individual scientist to download a single copy of this electronic file and reproduce up to 20 paper copies for noncommercial purposes advancing science and education, including classroom use, providing all reproductions include the complete content shown here, including the author information. All other forms of reproduction and/or transmittal are prohibited without written permission from GSA Copyright Permissions.