Cathodoluminescence Applied to Ore Geology and Exploration

Baele, Jean-Marc; Decrée, Sophie; Rusk, Brian

doi:10.1002/9781119290544.ch6

Cited by 12 publications

(7 citation statements)

References 113 publications

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“…4i). Such dull and quenched luminescence is characteristic of carbonate minerals with high Fe and variable Mn concentrations (Pierson 1981;Machel and Burton 1991;Baele et al 2019), which is also consistent with the major-element chemistry of George Fisher and Shovel Flats carbonates (Fig. 7, Fig.…”

Section: Carbonate At George Fishersupporting

confidence: 79%

Differentiating between hydrothermal and diagenetic carbonate using rare earth element and yttrium (REE+Y) geochemistry: a case study from the Paleoproterozoic George Fisher massive sulfide Zn deposit, Mount Isa, Australia

et al. 2021

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Carbonate minerals are ubiquitous in most sediment-hosted mineral deposits. These deposits can contain a variety of carbonate types with complex paragenetic relationships. When normalized to chondritic values (CN), rare-earth elements and yttrium (REE+YCN) can be used to constrain fluid chemistry and fluid-rock interaction processes in both low- and high-temperature settings. Unlike other phases (e.g., pyrite), the application of in situ laser ablation-inductively coupled plasma-mass spectroscopy (LA-ICP-MS) data to the differentiation of pre-ore and hydrothermal carbonates remains relatively untested. To assess the potential applicability of carbonate in situ REE+Y data, we combined transmitted light and cathodoluminescence (CL) petrography with LA-ICP-MS analysis of carbonate mineral phases from (1) the Proterozoic George Fisher clastic dominated (CD-type) massive sulfide deposit and from (2) correlative, barren host rock lithologies (Urquhart Shale Formation). The REE+YCN composition of pre-ore calcite suggests it formed during diagenesis from diagenetic pore fluids derived from ferruginous, anoxic seawater. Hydrothermal and hydrothermally altered calcite and dolomite from George Fisher is generally more LREE depleted than the pre-ore calcite, whole-rock REE concentrations, and shale reference values. We suggest this is the result of hydrothermal alteration by saline Cl--rich mineralizing fluids. Furthermore, the presence of both positive and negative Eu/Eu* values in calcite and dolomite indicates that the mineralizing fluids were relatively hot (>250°C) and cooled below 200–250°C during ore formation. This study confirms the hypothesis that in situ REE+Y data can be used to differentiate between pre-ore and hydrothermal carbonate and provide important constraints on the conditions of ore formation.

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Section: Carbonate At George Fishersupporting

confidence: 79%

Differentiating between hydrothermal and diagenetic carbonate using rare earth element and yttrium (REE+Y) geochemistry: a case study from the Paleoproterozoic George Fisher massive sulfide Zn deposit, Mount Isa, Australia

et al. 2021

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“…Most K-feldspar phenocrysts are turbid and, in CL images (Fig. 6), exhibit distinct red luminescence, characteristic of fenitization (Mariano & King, 1975;Finch & Klein, 1999;Mariano & Mariano, 2014;Elliott et al 2018;Baele et al 2019), becoming progressively browner with higher degrees of alteration to fine-grained clay minerals. Mineralized samples are typically brecciated (Fig.…”

Section: Breccias Associated With the Songwe-mauze Complexmentioning

confidence: 99%

Enrichment of heavy REE and Th in carbonatite-derived fenite breccia

et al. 2021

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Enrichment of the heavy rare earth elements (HREE) in carbonatites is rare as carbonatite petrogenesis favours the light (L)REE. We describe HREE enrichment in fenitized phonolite breccia, focusing on small satellite occurrences 1–2 km from the Songwe Hill carbonatite, Malawi. Within the breccia groundmass, a HREE-bearing mineral assemblage comprises xenotime, zircon, anatase/rutile and minor huttonite/thorite, as well as fluorite and apatite. A genetic link between HREE mineralization and carbonatite emplacement is indicated by the presence of Sr-bearing carbonate veins, carbonatite xenoliths and extensive fenitization. We propose that the HREE are retained in hydrothermal fluids which are residually derived from a carbonatite after precipitation of LREE minerals. Brecciation provides a focusing conduit for such fluids, enabling HREE transport and xenotime precipitation in the fenite. Continued fluid–rock interaction leads to dissolution of HREE-bearing minerals and further precipitation of xenotime and huttonite/thorite. At a maximum Y content of 3100 µg g−1, HREE concentrations in the presented example are not sufficient to constitute ore, but the similar composition and texture of these rocks to other cases of carbonatite-related HREE enrichment suggests that all form via a common mechanism linked to fenitization. Precipitation of HREE minerals only occurs where a pre-existing structure provides a focusing conduit for fenitizing fluids, reducing fluid – country-rock interaction. Enrichment of HREE and Th in fenite breccia serves as an indicator of fluid expulsion from a carbonatite, and may indicate the presence of LREE mineralization within the source carbonatite body at depth.

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“…The main difference is in the penetration depth of the different particles; CL typically samples the near-surface volume of the material, of the order of 1 µm, depending on the acceleration voltage of the electron beam and the sample composition. There are several ways by which CL in semiconductors or insulators is produced 25 – 27 : (1) band-to-band transitions, (2) band- to-defect transitions i.e. trapping of charge by a defect, (3) trap-assisted, band-to-band transitions, and (4) intra-defect transitions.…”

Section: Previous Studies On Cathodoluminescence In Feldsparmentioning

confidence: 99%

Site-selective mapping of metastable states using electron-beam induced luminescence microscopy

Kumar

Martin

Poelman

et al. 2020

Sci Rep

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Metastable states created by electron or hole capture in crystal defects are widely used in dosimetry and photonic applications. Feldspar, the most abundant mineral in the Earth’s crust (> 50%), generates metastable states with lifetimes of millions of years upon exposure to ionizing radiation. Although feldspar is widely used in dosimetry and geochronometry, the creation of metastable states and charge transfer across them is poorly understood. Understanding such phenomena requires next-generation methods based on high-resolution, site-selective probing of the metastable states. Recent studies using site-selective techniques such as photoluminescence (PL), and radioluminescence (RL) at 7 K have revealed that feldspar exhibits two near-infrared (NIR) emission bands peaking at 880 nm and 955 nm, which are believed to arise from the principal electron-trapping states. Here, we map for the first time the electron-trapping states in potassium-rich feldspar using spectrally-resolved cathodoluminescence microscopy at a spatial resolution of ~ 6 to 22 µm. Each pixel probed by a scanning electron microscope provides us a cathodoluminescence spectrum (SEM-CL) in the range 600–1000 nm, and elemental data from energy-dispersive x-ray (EDX) spectroscopy. We conclude that the two NIR emissions are spatially variable and, therefore, originate from different sites. This conclusion contradicts the existing model that the two emissions arise from two different excited states of a principal trap. Moreover, we are able to link the individual NIR emission peaks with the geochemical variations (K, Na and Fe concentration), and propose a model that explains the quenching of the NIR emission by Fe4+. Our study contributes to an improved understanding of charge storage in feldspathic minerals, with implications for developing sub-single grain (micrometer scale) measurement techniques in radiation dosimetry.

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Cathodoluminescence Applied to Ore Geology and Exploration

Cited by 12 publications

References 113 publications

Differentiating between hydrothermal and diagenetic carbonate using rare earth element and yttrium (REE+Y) geochemistry: a case study from the Paleoproterozoic George Fisher massive sulfide Zn deposit, Mount Isa, Australia

Differentiating between hydrothermal and diagenetic carbonate using rare earth element and yttrium (REE+Y) geochemistry: a case study from the Paleoproterozoic George Fisher massive sulfide Zn deposit, Mount Isa, Australia

Enrichment of heavy REE and Th in carbonatite-derived fenite breccia

Site-selective mapping of metastable states using electron-beam induced luminescence microscopy

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