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Analytical protocols for measurements of isotope ratios involving low-abundance isotopes 174 Hf (~ 0.16%), 180 W (~ 0.12%), and 190 Pt (~ 0.014%) using multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) at ca. tenfold improved precision compared to previous studies are presented. The improvements in precision result in part from the use of Faraday amplifiers equipped with 10 12 Ω resistors for collection of the isotope beams of interest, as well as for the isotope beams used to monitor isobaric interferences. For ion currents > 5 × 10 − 13 A (> 50 mV on an amplifier with 10 11 Ω resistor), uncertainties (2 s.d.) of better than 100 ppm are typically achieved for isotope ratios involving 174 Hf, 180 W and 190 Pt. Terrestrial isotope abundances (atomic percent ± 2 s.d.) of 174 Hf (0.16106 ± 0.00006; n = 15); 180 W (0.11910 ± 0.00009; n = 10); and 190 Pt (0.01286 ± 0.00005; n = 9) were determined on reference solutions throughout multiple analytical sessions over ~ 3 years. The results, however, rely on the accuracy of the reference value chosen for the isotope ratios employed for mass bias correction and, to a lesser extent, on the accuracy of the exponential mass fractionation law used for mass bias correction. For the precise determination of isotope ratios involving 174 Hf, 180 W and 190 Pt in natural materials, efficient chromatographic separation schemes for Hf and W from silicate-rich matrices, and for Pt from iron meteorite matrices, are presented that provide effective separation of the element of interest from interfering elements. First results for Pt suggest that IAB, IIAB and IIIAB iron meteorites exhibit terrestrial 190 Pt abundances within uncertainty. Three chondrite samples exhibit indistinguishable 174 Hf from terrestrial Hf. The isotope abundance of 180 W in meteorites is more variable due to radiogenic 180 W that was produced by 184 Os-decay. [ABSTRACT FROM AUTHOR]

It has long been recognized that the stable oxygen isotope 18O/16O ratios of chemical sediments show a systematic decrease with increasing age. This continuous, 3.8 Ga long secular trend has been attributed to 80 °C hot early Earth oceans, a ~15‰ lower 18O/16O ratio of Archean seawater, or diagenetic obliteration of the original isotope signal. We demonstrate that high-precision triple oxygen isotope measurements including the rare third stable oxygen isotope 17O on silica rocks (cherts) can be used to shed light on this major problem in geochemistry. Our triple oxygen isotope data do not support 80 °C hot oceans in the Archean. The data also exclude that the 18O/16O of seawater was much lower in the Archean. Also, a simple freshwater-origin of cherts is not supported by the new data. We discuss the effects of diagenetic alteration on the triple oxygen isotope compositions of cherts and show that the Archean and Proterozoic cherts could have equilibrated with fluids with higher 18O/16O than today's oceans. For the Archean cherts, the high 18O/16O fluids required to explain the observations could reflect the composition of ambient seawater or of modified hydrothermal fluids. Oceans with higher 18O/16O ratio would be expected for an Archean "water world" without large continents. High 18O/16O fluids, however, could also have formed locally by reactions between seawater and the oceanic crust. Our study shows that high-precision triple oxygen isotope data provide new understandings of processes deep in time. [ABSTRACT FROM AUTHOR]