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Paper No. 2
Presentation Time: 2:00 PM

ACCURACY OF THE U-PB SYSTEM: TRACER CALIBRATIONS, DECAY CONSTANTS AND OTHER PARAMETERS


CONDON, Daniel1, MCLEAN, Noah2, SCHOENE, Blair3, BOWRING, S.4, MATTINSON, James M.5, HIESS, J.1, NOBLE, S.R.1, SCHMITZ, M.D.6, CROWLEY, J.L.7 and PARRISH, Randall1, (1)NERC Isotope Geoscience Laboratory, British Geological Survey, Keyworth, Nottingham, NG12 5GG, United Kingdom, (2)Earth, Atomospheric, and Planetary Sciences, MIT, 77 Massachusetts Ave, Cambridge, MA 02139, (3)Department of Geosciences, Princeton University, Guyot Hall, Princeton, NJ 08544, (4)Dept. of Earth, Atmospheric & Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, (5)Earth Science, Univ of California, Santa Barbara, CA 93106-9630, (6)Department of Geosciences, Boise State University, Boise, ID 83725, (7)Department of Geosciences, Boise State University, 1910 University Drive, Boise, ID 83725, dcondon@bgs.ac.uk

The accuracy of the U-Pb system as a chronometer is largely controlled by the following factors: (1) our ability to determine accurate U to radiogenic Pb ratios (238U/206Pb* and 235U/207Pb*) in samples, including correcting for common Pb; (2) how well we know the 238U and 235U decay constants, and (3) closed-system behaviour (with respect to U and Pb) of the material being analysed. Under the auspices of the EARTHTIME initiative a series of experiments have been carried out aimed at assessing each of these components of the U-Pb system via analyses of closed system minerals.

U-Pb analyses by isotope dilution thermal ionisation mass spectrometry (ID-TIMS) exploit mixed U-Pb tracers (202Pb±205Pb±233235U) that allow for accurate determination of the sample U/Pb ratio through independent U and Pb mass spectrometric measurements. We report a comprehensive tracer calibration exercise using multiple mixed U-Pb gravimetric reference solutions made from high-purity metals, and re-determination of the isotopic composition of uranium reference materials that are used to quantify mass fractionation during the calibration exercise and subsequent sample analyses.

High-precision 238U/206Pb* and 235U/207Pb* determinations made on closed system materials, such as zircon that has undergone the ‘chemical abrasion’ technique, afford an opportunity to quantify λ238U/ λ235U and thus determine λ235U with uncertainties exceeding those of the original counting experiments of Jaffey et al (1971). We will summarise two recent studies which arrive at a reproducible revision of the Jaffey et al. decay constants.

Finally, recent studies have demonstrated the potential for per-mil level variation in 238U/235U in low-temperature geochemical systems. The magnitude of this effect in high temperature petrologic systems and its implication for geochronology is unknown. We will present preliminary results of coupled U-Pb and 238U/235U measurements for a suite of closed system zircons as a means to assess the effect of natural variability in 238U/235U for high-precision geochronology.

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