Résumé
A critical problem for conducting quantitative analysis of individual fluid inclusions using Synchrotron X-Ray Fluorescence (SXRF) technique relates to the standardization and the calibration of the X-ray spectra. In this study, different approaches have been tested for calibration purposes: (a) the use of chlorine when Cl content can be estimated either from melting point depressions of undersaturated fluid inclusions or from saturation limits for halite-bearing fluid inclusions, (b) the use of calcium from synthetic fluid inclusions of known CaCl2 content as an external standard. SXRF analysis was performed on individual fluid inclusions from the Chivor and Guali emerald deposits, Columbia. These well-known samples contain a single fluid inclusion population for which detailed crush-leach analyses are available, thus providing a relevant compositional reference frame. Concentration estimates were also compared to Particle Induced X-ray Emission (PIXE) analysis carried out independently on the same fluid inclusions.Results of the calibration tests indicate that major (Cl, K, Ca, Fe, Mn) and trace element (Cu, Zn, As, Br, Rb, Sr, Ba, Pb) concentration estimates can be performed without precise knowledge of the analytical volume and the inclusion’s 3D geometry. Although the standard deviation of the SXRF results can be relatively high depending on the calibration mode used, mean concentration estimates for most elements are in good agreement with PIXE and crush-leach analysis. Elemental distributions within single fluid inclusions were also established. Associated correlation diagrams argue for the homogeneous distribution of most elements in the fluid inclusion. In contrast, Br shows a bimodal distribution interpreted to reflect a significant enrichment of the vapor portion of the inclusion fluid.