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Abstract:This article concerns application of cathodoluminescence~CL! spectroscopy to volcanic quartz and its utility in assessing variation in trace quantities of Ti within individual crystals. CL spectroscopy provides useful details of intragrain compositional variability and structure but generally limited quantitative information on element abundances. Microbeam analysis can provide such information but is time-consuming and costly, particularly if large numbers of analyses are required. To maximize advantages of both approaches, natural and synthetic quartz crystals were studied using high-resolution hyperspectral CL imaging~1.2-5.0 eV range! combined with analysis via laser ablation inductively coupled plasma mass spectrometry~LA-ICPMS!. Spectral intensities can be deconvolved into three principal contributions~1.93, 2.19, and 2.72 eV!, for which intensity of the latter peak was found to correlate directly with Ti concentration. Quantitative maps of Ti variation can be produced by calibration of the CL spectral data against relatively few analytical points. Such maps provide useful information concerning intragrain zoning or heterogeneity of Ti contents with the sensitivity of LA-ICPMS analysis and spatial resolution of electron microprobe analysis.

Sheet AA2024-T3 is probably one of the most studied aluminium alloys in the corrosion field, because, with copper as an alloying addition, it is one of the most corrosion-prone aluminium alloys. This paper reports new findings on the composition and distribution of intermetallic (IM) particles in AA2024-T3 through the examination of over 80 000 compositional domains in nearly 18 000 IM particles. This work was achieved by using an electron microprobe to map out 2 × 2 mm 2 at a step size of 400 nm. This study revealed that the composition of individual particles can vary considerably from 'accepted' compositions. Domains within particles were extensive across the surface. Because such a large area was mapped, it was possible to subdivide this area and to look at the variation of particle statistics from region to region, providing some information on the statistical variation for small electrodes.

New geological, bulk chemical and mineralogical (QEMSCAN and FEG-EPMA) data are presented for albitite-type uranium deposits of the Mount Isa region of Queensland, Australia. Early albitisation of interbedded metabasalt and metasiltstone predated intense deformation along D 2 high strain (mylonite) zones. The early sodic alteration paragenetic stage includes albite, riebeckite, aegirine, apatite, zircon and magnetite. This paragenetic stage was overprinted by potassic microveins, containing K-feldspar, biotite, coffinite, brannerite, rare uraninite, ilmenite and rutile. An unusual U-Zr phase has also been identified which exhibits continuous solid solution with a uranium silicate possibly coffinite or nenadkevite. Calcite, epidote and sulphide veinlets represent the latest stage of mineralisation. This transition from ductile deformation and sodic alteration to vein-controlled uranium is mirrored in other examples of the deposit type. The association of uranium with F-rich minerals and a suite of high field strength elements; phosphorous and zirconium is interpreted to be indicative of a magmatic rather than metamorphic or basinal fluid source. No large intrusions of appropriate age outcrop near the deposits; but we suggest a relationship with B-and Be-rich pegmatites and quartz-tourmaline veins.

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