Unlocking the applications of automated mineral analysis

Identifying and quantifying the relative abundance of minerals is a fundamental part of many aspects of both pure and applied geology. Historically, quantitative mineralogy could be achieved using optical microscopy and point counting. This is a slow and operator dependent process, and practically impossible to achieve in, for example, very fine grained samples. Over the last decade a range of automated mineralogy technologies have arisen from the global mining industry and are being increasingly used in other branches of geology. These technologies, based on scanning electron microscopy with linked energy dispersive spectrometers, have the potential to revolutionise how we quantify mineralogy. In addition, during measurement, the sample textures are also captured, providing a wealth of valuable data for the geologist. In this article we review the current state of automated mineralogy and highlight the many areas of application for this technology.     

An archaean granulite-grade tonalite-trondhjemite-granite suite from scourie,NW Scotland: Geochemistry and origin

The Lewisian complex of the Scourie-Badcall area is composed predominantly of banded tonalitic gneiss which intrudes layered gabbro-ultramafic complexes. Intrusive into both gabbro and tonalitic gneiss are homogeneous acid sheets which are trondhjemitic to granitic in composition. All rocks were subjected to granulite facies metamorphism. Smooth continuous trends on chemical variation diagrams suggest that the evolution of these rocks was dominated by fractional crystallisation. A scheme is proposed whereby a tonalitic melt was parental to trondhjemite and granite. Variation within tonalites was a function of the fractional crystallisation of hornblende and plagioclase, and trondhjemite was derived from tonalite by the fractional crystallisation of hornblende and/or plagioclase. Granite and granodiorite represent residual liquids which evolved along the quartz-feldspar cotectic surface; they were derived by the fractional crystallisation of plagioclase from a trondhjemite liquid. Some trondhjemitic sheets are quartz-plagioclase residues from which a granitic melt was removed. The associated gabbros and ultramafic rocks are not directly related to the proposed fractional crystallisation scheme and are not crystal residues removed from the tonalitic melt. Tonalites were probably derived from a basaltic source by partial melting or fractional crystallisation with either hornblende and/or garnet as residual phases.     

Ophiolitic trondhjemites: a possible analogue for Hadean felsic 'crust'

It has been argued that >4.0 Ga detrital zircons preserved in sediments of the Jack Hills, western Australia, preserve evidence for a well‐developed continental crust on the Earth at 4.4–4.5 Ga ago. Here, it is shown that there are geochemical similarities between the Jack Hills zircons and the zircons found in trondhjemites in ophiolite sequences, suggesting that the Earth's first felsic crust may have formed in a manner analogous to modern ophiolitic trondhjemites. The trondhjemites of the Oman ophiolite were formed by the hydrous partial melting of the upper (hornblende) gabbros in the roof‐zone of an axial magma chamber. A similar hydrous melting of a mafic protolith may have operated during the Hadean, to create small volumes of felsic rocks within a dominantly mafic crust, obviating the need to postulate a felsic continental crust at 4.4–4.5 Ga.     

William Smith's map brought alive by digital remastering

The geological mapping carried out by William Smith, which resulted in the publication of his famous map in 1815, was remarkable in many respects, not least because it relied on him being able to make consistent and accurate observations on the rock types he encountered during his fieldwork. This ability, gained from his many years studying rocks, allowed him to observe features with his own eyes (or at the very least, with the aid of a simple magnifying device) that others could not. We take a new look at William Smith's original stratigraphical sequences, and with samples collected from his classic field areas (many of which are around the city of Bath, Somerset, UK), demonstrate how spatial mineralogy mapping can be incorporated into the modern age of digital mapping.     

The fusion crust of the Winchcombe meteorite: A preserved record of atmospheric entry processes

Fusion crusts form during the atmospheric entry heating of meteorites and preserve a record of the conditions that occurred during deceleration in the atmosphere. The fusion crust of the Winchcombe meteorite closely resembles that of other stony meteorites, and in particular CM2 chondrites, since it is dominated by olivine phenocrysts set in a glassy mesostasis with magnetite, and is highly vesicular. Dehydration cracks are unusually abundant in Winchcombe. Failure of this weak layer is an additional ablation mechanism to produce large numbers of particles during deceleration, consistent with the observation of pulses of plasma in videos of the Winchcombe fireball. Calving events might provide an observable phenomenon related to meteorites that are particularly susceptible to dehydration. Oscillatory zoning is observed within olivine phenocrysts in the fusion crust, in contrast to other meteorites, perhaps owing to temperature fluctuations resulting from calving events. Magnetite monolayers are found in the crust, and have also not been previously reported, and form discontinuous strata. These features grade into magnetite rims formed on the external surface of the crust and suggest the trapping of surface magnetite by collapse of melt. Magnetite monolayers may be a feature of meteorites that undergo significant degassing. Silicate warts with dendritic textures were observed and are suggested to be droplets ablated from another stone in the shower. They, therefore, represent the first evidence for intershower transfer of ablation materials and are consistent with the other evidence in the Winchcombe meteorite for unusually intense gas loss and ablation, despite its low entry velocity.     

The geochemistry of mantle chromitites from the northern part of the Oman ophiolite: inferred parental melt compositions

Chromitites from a single section through the mantle in the Oman ophiolite are of two different types. Low-cr# chromitites, of MORB affinity are found in the upper part of the section, close to the Moho. High-cr# chromitites, with arc affinities are found deeper in the mantle. Experimental data are used to recover the compositions of the melts parental to the chromitites and show that the low-cr# chromitites were derived from melts with 14.5–15.4 wt% Al₂O₃, with 0.4 to 0.9 wt% TiO₂ and with a maximum possible mg# of 0.76. In contrast the high-cr# chromitites were derived from melts with 11.8–12.9 wt% Al₂O₃, 0.2–0.35 wt% TiO₂ and a maximum melt mg# of 0.785. Comparison with the published compositions of lavas from the Oman ophiolite shows that the low-cr# chromitites may be genetically related to the upper (Lasail, and Alley) pillow lava units and the high-cr# chromitites the boninites of the upper pillow lava Alley Unit. The calculated TiO₂–Al₂O₃ compositions of the parental chromitite magmas indicate that the high-cr# chromitites were derived from high-Ca boninitic melts, produced by melting of depleted mantle peridotite. The low-cr# chromitites were derived from melts which were a mixture of two end-members—one represented by a depleted mantle melt and the other represented by MORB. This mixing probably took place as a result of melt–rock reaction. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Chromite in the mantle section of the Oman ophiolite: A new genetic model

Abstract   This paper reviews the compositional data (major elements, platinum group element [PGE] concentrations, Os- and O-isotopes) for chromites from the mantle section of the Oman ophiolite. Chromites in chromitite from the Oman ophiolite lie on a compositional spectrum between high-Cr♯, boninite-like and low-Cr♯, mid-oceanic ridge basalt-like end-members. The high-Cr♯ end-member is low in Ti, has a fractionated PGE pattern and is enriched in iridium group-platinum group elements (IPGE). The low-Cr♯ end-member has higher Ti and an unfractionated PGE pattern. The compositional variation in the chromitites reflects their crystallization from a range of different melt compositions. It is proposed that this wide variation in melt compositions was produced by the process of a melt–rock reaction, whereby a basaltic melt has reacted with harzburgitic mantle to yield successively more Cr-rich melts. In contrast to previous models, this approach does not require a change in the tectonic environment to explain the different chromite types.     

Determination of Fe<Superscript>3+</Superscript>/ΣFe ratios in chrome spinels using a combined Mössbauer and single-crystal X-ray approach: application to chromitites from the mantle section of the Oman ophiolite

We present the results of a comparative study in which we have measured Fe³⁺/ΣFe ratios in chromites from mantle chromitites in the Oman ophiolite using Mössbauer spectroscopy and single-crystal X-ray diffraction. We have compared these results with ratios calculated from mineral stoichiometry and find that mineral stoichiometry calculations do not accurately reflect the measured Fe³⁺/ΣFe ratios. We have identified three groups of samples. The majority preserve Fe³⁺/ΣFe ratios which are thought to be magmatic, whereas a few samples are highly oxidized and have high Fe³⁺/ΣFe ratios. There is also a group of partially oxidized samples. The oxidized chromites show anomalously low cell edge (a ₀) values and their oxygen positional parameters among the lowest ever found for chromites. Site occupancy calculations show that some chromites are non-stoichiometric and contain vacancies in their structure randomly distributed between both the T and M sites. The field relationships suggest that the oxidation of the magmatic chromitites took place in association with a ductile shear zone in mantle harzburgites. Primary magmatic Fe³⁺/ΣFe ratios measured for the Oman mantle chromitites are between 0.193–0.285 (X-ray data) and 0.164–0.270 (Mössbauer data) and preserve a range of Fe³⁺/ΣFe ratios which we propose is real and reflects differences in the composition of the magmas parental to the chromitites. The range of values extends from those MORB melts (0.16 ± 0.1) to those for arc basalts (0.22–0.28).