ACCURACY OF THE U-PB SYSTEM: TRACER CALIBRATIONS, DECAY CONSTANTS AND OTHER PARAMETERS
U-Pb analyses by isotope dilution thermal ionisation mass spectrometry (ID-TIMS) exploit mixed U-Pb tracers (202Pb±205Pb±233U±235U) 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.