Measurement of SLAP2 and GISPδ17O and proposed VSMOW-SLAP normalization forδ17O and17Oexcess

RATIONALE The absence of an agreed-upon δ(17)O value for the primary reference water SLAP leads to significant discrepancies in the reported values of δ(17)O and the parameter (17)O(excess). The accuracy of δ(17)O and (17)O(excess) values is significantly improved if the measurements are normalized using a two-point calibration, following the convention for δ(2)H and δ(18)O values. METHODS New measurements of the δ(17)O values of SLAP2 and GISP are presented and compared with published data. Water samples were fluorinated with CoF(3). Helium carried the O(2) product to a 5A (4.2 to 4.4 A) molecular sieve trap submerged in liquid nitrogen. The O(2) sample was introduced into a dual-inlet ThermoFinnigan MAT 253 isotope ratio mass spectrometer for measurement of m/z 32, 33, and 34. The δ(18)O and δ(17) values were calculated after 90 comparisons with an O(2) reference gas. RESULTS We propose that the accepted δ(17)O value of SLAP be defined in terms of δ(18) O = -55.5 ‰ and (17)O(excess) = 0, yielding a δ(17)O value of approximately -29.6986 ‰ [corrected]. Using this definition for SLAP and the recommended normalization procedure, the δ(17)O value of GISP is -13.16 ± 0.05 ‰ and the (17)O(excess) value of GISP is 22 ± 11 per meg. Correcting previous published values of GISP δ(17)O to both VSMOW and SLAP improves the inter-laboratory precision by about 10 per meg. CONCLUSIONS The data generated here and compiled from previous studies provide a substantial volume of evidence to evaluate the various normalization techniques currently used for triple oxygen isotope measurements. We recommend that reported δ(17) O and (17)O(excess) values be normalized to the VSMOW-SLAP scale, using a definition of SLAP such that its (17)O(excess) is exactly zero.