Geology topics

Jay M. Thompson

Publications and source records attributed to Jay M. Thompson.

25 records · Page 2Linked to original sources

USGS2025

Formation of the Mount Weld rare earth deposit, Western Australia: Geochronology constraints

Constraining the age of protracted chemical weathering in stable cratonic areas that may form thick regoliths and the potential enrichment of various elements is challenging. Economic deposits of aluminium, iron, copper, nickel, cobalt, niobium, and rare earth elements (REEs) form in this manner. Determining the age of formation can provide key information for exploration of similar deposits as well as to better constrain paleoclimatic conditions. This study describes our effort to constrain the age of formation of the Mount Weld deposit, a world-class carbonatite-derived REE laterite deposit. We utilize multiple geochronological techniques on different minerals. The oldest dates, ranging from ca. 100 to 50 Ma, were from laser ablation ICPMS, Lu-Hf dating of churchite, a heavy REE phosphate mineral formed by mineral saturation in groundwater. Growth bands on individual minerals show a younging outwards. 40 Ar/ 39 Ar geochronology of cryptomelane, a potassium-bearing manganese oxide mineral, yielded ages ranging from ca. 40 to 26 Ma. Similarly, (U–Th)/He geochronology of goethite yielded ages from ca. 45 to 19 Ma.

Mount Weld deposit↗

USGS2025

Paleoproterozoic vein graphite mineralization caused by decarbonation in the Ruby Range, Montana, USA

Hydrothermal graphite veins are a possible source for modern battery materials and require better understanding of their carbon source(s) and absolute timing to develop mapable criteria for exploration models. We present new observations of graphite vein and alteration paragenesis and U-Pb LA-ICP-MS titanite age data from the Ruby prospect, Montana, USA, that constrain mineralization timing and source. The graphite veins cut high-temperature metamorphic rocks of the lower Christensen Range suite and are associated with intense diopside (Di0.69Hd0.27Jo0.04) alteration of marble. The oldest titanite ages in fresh marble and partially altered calc-silicate gneiss are ca. 2,500 – 2,450 Ma, show elevated REE values, and Eu/Eu* <1.5, consistent with growth during early regional metamorphism. Titanite in diopside-graphite alteration, interpreted as part of the hydrothermal vein-forming episode, cluster around 1,750 Ma, are characterized by lower REE values, and show Eu/Eu* >2; suggesting a low fO 2 fluid generated from metamorphism during the Big Sky orogeny. Our paragenetic observations and titanite ages indicate graphite vein formation via skarnoid decarbonation reactions in marble late in regional orogenesis. Granulite-facies, carbonate-bearing, supracrustal rock terranes are thus favorable for hydrothermal graphite vein deposits.

Montana↗

USGS2025

Stable isotope composition and geochemistry of calcite and dolomite in the Mountain Pass carbonatite: A lens into petrogenesis

Carbonatites host most of the global rare earth element (REE) deposits. The petrogenesis of these rocks, including magmatic and post-magmatic processes, are poorly understood but critical in forming and upgrading these deposits. The Mountain Pass carbonatite, which hosts the only active REE mine in North America, is lithologically variable but consistently contains >50% calcite and/or dolomite. Multiple generations of carbonates are evident, suggesting bulk analysis of carbonate minerals would generate a mixed isotopic and geochemical signature. In-situ stable carbon and oxygen isotopes, combined with geochemical analysis and petrography, distinguish carbonate generations, trace the source region of the carbonatite magma, and link carbonate genesis to REE mineralization throughout the intrusion. Primary carbon and oxygen isotope values outside the accepted mantle range may suggest a subduction-related carbon and oxygen source in the mantle. Deformation textures in primary calcite indicate syn- or post-crystallization ductile flow. Carbonates with secondary textures and heavy δ 13 C and δ 18 O values are associated with ore mineralization, suggesting fluid mobilization was important in concentrating REE and upgrading of the Mountain Pass deposit.

California↗

USGS2025

Niobium-rich minerals from the Sheep Creek carbonatite-related deposits, Montana, USA

The Sheep Creek area in southwest Montana contains a number of small, tabular, carbonatite-related deposits that are rich in Nb- and REE-minerals. Two of the “vein-dikes” were mined at a small scale for Nb in the late 1950s. The most abundant Nb-bearing minerals are columbite-(Fe), nioboaeschynite-(Ce), baotite, and two varieties of Ti-Nb-Fe-oxide. An early oxide with Ti/Nb (atomic) near unity later broke down to a mixture of columbite + TiO2 with distinctly lower Nb content. Zircon intergrown with the Nb-REE minerals was dated by U-Pb methods to 116±2 Ma. This age is in agreement with previous dating (Th-Pb on monazite, Re-Os on molybdenite), and indicates that the Sheep Creek deposits are early Cretaceous in age.

Montana↗

USGS2024

Compositional and structural mapping of Northwest Africa 15507 angrite

Angrite meteorites represent interesting sampling of planetary crustal environments. Quench-textured angrites with strong crystal zoning originated from the shallow surface region, with evidence of reducing conditions during solidification. Plutonic angrites have more coarse-grained igneous and metamorphic textures with comparatively less zoning and are interpreted as having equilibrated at greater depth. Plutonic angrites contain the minerals magnetite Fe 3 O 4 comprised of Fe 2+ and Fe 3+ , and rhönite, where Fe 3+ is required by inspection of mineral stoichiometry. NWA 15507 is a plutonic angrite with a microgabbroic texture (mean grainsize ∼1.4 mm) composed of zoned Al-Ti-augite, Ca-bearing olivine, anorthite, with accessory kirschsteinite, rhönite, hercynite, low-Ni kamacite, merrillite, Ti-free magnetite and troilite [ 1 ]. Rhönite analyzed by electron-probe microanalysis (EPMA) has the formula Ca 2.04 (Mg 0.32 Fe 2+ 4.25 Fe 3+ 0.47 Ti 0.33 Al 0.61 )(Si 3.74 Al 2.26 )O 20 , where Fe 3+ was estimated by stoichiometric analysis. During preliminary cathodoluminescence (CL) analysis, complex subgrain and oscillatory zoning was observed in the anorthite. In this study we use a combined approach of electron probe microanalysis (EPMA), cathodoluminescence (CL), electron-backscatter diffraction (EBSD), and laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) to further investigate the anorthite and distribution of Fe 3+ in NWA 15507.

Microscopy and Microanalysis↗

USGS2023

Hyperspectral cathodoluminescence and quantitative EPMA mapping of angrite northwest Africa 15507

Angrite meteorites represent alkali depleted planetary crust of basaltic composition, and have both plutonic and volcanic lithologies. NWA 15507 is a microgabbroic specimen (mean grainsize ~1.4 mm) composed predominantly of zoned Al-Ti-augite, Ca-bearing olivine and anorthite together with accessory kirschsteinite, rhönite, hercynite, low-Ni kamacite, merrillite, magnetite and troilite. Upon initial investigation, the anorthite was found to exhibit a cathodoluminescence (CL) response which revealed a complex history of crystallization. Hyperspectral cathodoluminescence, quantitative electron probe microanalysis mapping, laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), and electron back scattered diffraction (EBSD) were used to determine the CL emitter to better unravel the crystallization history of NWA 15507.

Conference Paper↗

USGS2023

The Mount Weld rare earth element deposit, Western Australia: A carbonatite-derived laterite

Carbonatite-hosted rare earth element (REE) deposits are the primary source of the world’s light REEs and have the potential to be a source of heavy REEs. The Mount Weld REE deposit in Western Australia is hosted in a lateritic sequence that reflects supergene enrichment of the underlying carbonatite complex. Similar to other carbonatite-related ore deposits, ore from Mount Weld displays extreme light REE (LREE) enrichment (La up to 4 wt. %), but in contrast also contains substantially higher concentrations of heavy REEs (HREEs). REE enrichment in the laterite is controlled by the breakdown of primary minerals, the release and transport of REEs, and the formation of secondary minerals. Secondary REE-bearing phosphate minerals are the primary REE-host phases in the laterite ore with monazite as the dominant phase; other REE-bearing phases include rhabdophane, cerianite, churchite, florencite, and crandallite subgroup minerals. Profiles through the laterite show that in the REE-rich zone, apatite and primary calcite have broken down, and dolomite decreases by approximately 60-100%, such that the loss of Ca and Mg, as well as Si and K, leads to a relative increase in the REEs. Sequestering of REEs in secondary mineral phases formed by groundwater further enhances the REE concentration.

Mount Weld mine↗