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Proposed Title 1: - Queen's University

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Stable isotopic compositions of C and O in calcite and dolomite were made using a<br />

Gas Bench coupled to a ThermoFinnigan Delta plus XP mass spectrometer and are reported<br />

in the δ notation in units of per mil relative to V-PDB and V-SMOW, respectively. The<br />

isotopic compositions of C and O in the fluid were calculated from the fractionation factor<br />

of Ohmoto and Rye (1979) and Hu and Clayton (2003), respectively.<br />

The content of REEs in uraninite was determined by LA-ICPMS using a<br />

ThermoFisher X-Series II. This instrument is equipped with a New Wave UP-213<br />

Nd:YAG laser-ablation system using a small volume (2.5 cm 3 ) and laminar-flow<br />

SuperCell ablation cell. Ablation was performed in an atmosphere of pure He (0.6<br />

l/min), with the ablated aerosol mixed with Ar (0.8 l/min) immediately after the ablation<br />

cell and prior to direct introduction into the torch. Pre-defined areas of the polished thin<br />

sections were ablated using a spot size of 30μm in diameter. Instrument drift was<br />

performed using NIST 612 and calibration was performed using zircon standard 91500<br />

(Wiedenbeck et al., 1995). The REE abundances are normalized to the abundances in<br />

chondrite meteorites reported by McDonough and Sun (1995). Heavy and light REE<br />

variations are reflected by chondrite normalized (La/Yb) N , (La/Sm) N and (Tb/Yb) N ratios,<br />

whereas redox conditions are recorded by Eu/Eu* and Ce/Ce* anomalies (DeBaar, 1991;<br />

Gao and Wedepohl, 1995).<br />

Mineral name abbreviations used in this chapter are those from Kretz (1983). The<br />

superscript numerical value on mineral name abbreviations reflects the mineral growth<br />

stage.<br />

89

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