The Coles Hill Uranium Deposit, Virginia, USA: Geology, Geochemistry, Geochronology, and Genetic Model

The Coles Hill uranium deposit, with an indicated resource of about 130 Mlb of U3O8, is the largest unmined uranium deposit in the United States. The deposit is hosted in the Taconian (approx. 480–450 Ma) Martinsville igneous complex, which consists of the Ordovician Leatherwood Granite (granodiorite) and the Silurian Rich Acres Formation (diorite). The host rock was metamorphosed to orthogneiss during the Alleghanian orogeny (approx. 325–260 Ma), when it also underwent dextral strike-slip movement along the Brookneal shear zone. During the Triassic, extensional tectonics led to the development of the Dan River Basin that lies east of Coles Hill. The mineralized zone is hosted in brittle structures in the footwall of the Triassic Chatham fault that forms the western edge of the basin. Within brittle fracture zones, uranium silicate and uranium-bearing fluorapatite with traces of brannerite form veins and breccia-fill with chlorite, quartz, titanium oxide, pyrite, and calcite. Uranium silicates also coat and replace primary titanite, zircon, ilmenite, and sulfides. Sodium metasomatism preceded and accompanied uranium mineralization, pervasively altering host rock and forming albite from primary feldspar, depositing limpid albite rims on igneous feldspar, altering titanite to titanium oxide and calcite, and forming riebeckite. Various geothermometers indicate temperatures of less than ~200°C during mineralization. In situ U-Pb analyses of titanite, Ti-oxide, and apatite, along with Rb/Sr and U/Pb isotope systematics of whole-rock samples, resolve the timing of geologic processes affecting Coles Hill. The host Leatherwood Granite containing primary euhedral titanite is dated at 450 to 445 Ma, in agreement with previously obtained ages from zircon in the Martinsville igneous complex. A regional metamorphic event at 330 to 310 Ma formed anhedral titanite and some apatite, reequilibrated whole-rock Rb/Sr and U-Pb isotopes, and is interpreted to have coincided with movement along the Brookneal shear zone. During shearing and metamorphism, primary refractory uranium-bearing minerals including titanite, zircon, and uranothorite were recrystallized, and uranium was liberated and mixed locally with hematite, clay, and other fine-grained minerals. Uranium mineralization was accompanied by a metasomatic episode between 250 and 200 Ma that reset the Rb-Sr and U-Pb isotope systems and formed titanium oxide and apatite that are associated and, in places, intimately intergrown with uranium silicate dating mineralization. This event coincides with rifting that formed the Dan River Basin and was a precursor to the breakup of Pangea. The orientation of late-stage tectonic stylolites is compatible with their formation during Late Triassic to Early Jurassic basin inversion, postdating the main stage of uranium mineralization and effectively dating mineralization as Mesozoic. Based on the close spatial and temporal association of uranium with apatite, we propose that uranium was carried as a uranyl-phosphate complex. Uranium was locally reduced by coupled redox reactions with ferrous iron and sulfide minerals in the host rock, forming uranium silicates. The release of calcium during sodium metasomatic alteration of primary calcic feldspar and titanite in the host rock initiated successive reactions in which uranium and phosphate in mineralizing fluids combined with calcium to form U-enriched fluorapatite. Based on the deposit mineralogy, oxygen isotope geochemistry, and trace element characteristics of uranium silicate and gangue minerals, the primary mineralizing fluids likely included connate and/or meteoric water sourced from the adjacent Dan River Basin. High heat flow related to Mesozoic rifting may have driven these (P-Na-F-rich) fluids through local aquifers and into basin margin faults, transporting uranium from the basin or mobilizing uranium from previously formed U minerals in the Brookneal shear zone, or from U-enriched older basement rock.

The Perron Gold Deposit, Archean Abitibi Belt, Canada: Exceptionally High-Grade Mineralization Related to Higher Gold-Carrying Capacity of Hydrocarbon-Rich Fluids

The Perron deposit, an Archean orogenic gold deposit located in the Abitibi belt, hosts a quartz vein-type gold-bearing zone, known as the high-grade zone (HGZ). The HGZ is vertically continuous along >1.2 km, and is exceptionally rich in visible gold throughout its vertical extent, with grades ranging from 30 to 500 ppm. Various hypotheses were tested to account for that, such as: (1) efficient precipitating mechanisms; (2) gold remobilization; (3) particular fluids; (4) specific gold sources for saturating the fluids; and (5) a different mineralizing temperature. Host rocks recorded peak metamorphism at ~600 °C based on an amphibole geothermometer. Visible gold is associated with sphalerite (<5%) which precipitated at 370 °C, based on the sphalerite GGIMFis geothermometer, during late exhumation of verticalized host rocks. Pyrite chemistry analyzed by LA-ICP-MS (Laser Ablation Inductively Coupled Plasma Mass Spectrometry) is comparable to classical orogenic gold deposits of the Abitibi belt, without indication of a possible magmatic fluid and gold contribution. Comparison of pyrite trace element signatures for identifying a potential gold source was inconclusive to demonstrate that primary base-metal rich volcanogenic gold mineralization, dispersed in the host rhyolitic dome, could be the source for the later formation of the HGZ. Rather, nodular pyrites in graphitic shales, sharing similar trace element signatures with pyrite of the HGZ, are considered a potential source. The most striking outcome is the lack of water in the mineralizing fluids, implying that gold was not transported under aqueous complexes, even if fugacity of sulfur (−6) and oxygen (−28), and pH (~7) are providing the best conditions at a temperature of 350 °C for solubilizing gold in water. Fluid inclusions, analyzed by solid-probe mass spectrometry, are rather comparable to fossil gas composed mostly of hydrocarbons (methane and ethane and possibly butane and propane and other unidentified organic compounds), rich in CO2, with N2 and trace of Ar, H2S, and He. It is interpreted that gold and zinc were transported as hydrocarbon-metal complexes or as colloidal gold nanoparticles. The exceptional high content of gold and zinc in the HGZ is thus explained by the higher transporting capacity of these unique mineralizing fluids.

Tellurium and Selenium Mineralogy of Gold Deposits in Northern Fennoscandia

Mineralization of Te and Se was found in gold deposits and uranium occurrences, located in the Paleoproterozoic greenstone belts in Northern Fennoscandia. These deposits are of different genesis, but all of them formed at the late stages of the Svecofennian orogeny, and they have common geochemical association of metals Au, Cu, Co, U, Bi, Te, and Se. The prevalentTe minerals are Ni and Fe tellurides melonite and frohbergite, and Pb telluride altaite. Bismuth tellurides were detected in many deposits in the region, but usually not more than in two–three grains. The main selenide in the studied deposits is clausthalite. The most diversified selenium mineralization (clausthalite, klockmannite, kawazulite, skippenite, poubaite) was discovered in the deposits, located in the Russian part of the Salla-Kuolajarvi belt. Consecutive change of sulfides by tellurides, then by selenotellurides and later by selenides, indicates increase of selenium fugacity, fSe2, in relation to fTe2 and to fS2in the mineralizing fluids. Gold-, selenium-, and tellutium-rich fluids are potentially linked with the post-Svecofennian thermal event and intrusion of post-orogenic granites (1.79–1.75 Ga) in the Salla-Kuolajarvi and Perapohja belts. Study of fluid inclusions in quartz from the deposits in the Salla-Kuolajarvi belt showed that the fluids were high-temperature (240–>300 °C) with high salinity (up to 26% NaCl-eq.). Composition of all studied selenotellurides, kawazulite-skippenite, and poubaite varies significantly in Se/Te ratio and in Pb content. Skippenite and kawazulite show the full range of Se-Te isomorphism. Ni-Co and Co-Fe substitution plays an important role in melonite and mattagamite: high cobalt was detected in nickel telluride in the Juomasuo and Konttiaho, and mattagamites from Ozernoe and Juomasuo contain significant Fe.In the Ozernoe uranium occurrence, the main mineral-concentrator of selenium is molybdenite, which contains up to 16 wt.% of Se in the marginal parts of the grains. The molybdenite is rich in Re (up to 1.2 wt.%), and the impurity of Re is irregularly distributed in molybdenite flakes and spherulites.

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

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.

Analysis of tectonic fracturing in the Mibladen ore deposit (Upper Moulouya, Morocco) and its impact on the Pb-Ba mineralization emplacement

The MVT-type Pb-Ba mineralizations of the Mibladen ore deposit are hosted by Jurassic carbonates as well as Infracenomanian conglomerates and sandstones. The mineral paragenesis is mainly composed of galena and barite with lesser chalcopyrite and pyrite, accompanied by supergene oxidation minerals. This ore deposit is the result of a major epigenetic mineral stage with economic orebodies occuring as replacement of pre-existent carbonate rocks, fillings of karst cavities, interstratal joints, collapse-breccias, fractures and faults. Structural and microtectonic analyses we carried out in this ore deposit, allowed us to highlight two main fracture networks controlling ore deposition within karst cavities and interstratal joints: i) NNW-SSE to NNE-SSW trending tension gashes and normal faults; ii) ENE-WSW to E-W trending reverse faults with strike-slip components and transtensive relay zones. All of these structures are developed under a regional compressional tectonic regime divided into extensional and transtensional episodes (σ1-σ2 and σ2-σ3 permutations) with sub-meridian σ1 axis and sub-equatorial σ3 axis. This compressive tectonic event caused the uplift of Mibladen area and favored the circulation of mineralizing fluids along the NW-SE and ENE-WSW major faults such as Amourou and Aouli Faults, during the Infracenomanian period (Upper Jurassic-Early Cretaceous).

Influence of Titaniferous Phases on Tungsten Mineralizing Processes at the Giant Sisson Brook W-Mo Deposit, New Brunswick, Canada: Mineral-Chemical and Geochronological Assessment

The Sisson Brook deposit is a low-grade, large-tonnage W-Mo deposit with notable Cu located in west-central New Brunswick, Canada, and is one of several W-Mo deposits in New Brunswick associated with fluids sourced from granitic plutons emplaced during the Devonian Acadian Orogeny. The younger Devonian-aged stockwork and replacement scheelite-wolframite-molybdenite (and chalcopyrite) mineralization straddles the faulted boundary between Cambro-Ordovician metasedimentary rocks with Ordovician felsic volcaniclastic rocks and the Middle Silurian Howard Peak Granodiorite, with dioritic and gabbroic phases. U-Pb dating of magmatic titanite in the host dioritic phase of the Howard Peak Granodiorite using LA ICP-MS resulted in a 204Pb-corrected concordant age of 432.1 ± 1.9 Ma. Petrologic examination of selected mineralization combined with elemental mapping of vein selvages using micro-XRF and metasomatic titanite and ilmenite grains using LA ICP-MS indicates that saturation of titaniferous phases influenced the distribution of scheelite versus wolframite mineralization by altering the aFe/aCa ratio in mineralizing fluids. Ilmenite saturation in Ti-rich host rocks lowered the relative aFe/aCa and led to the formation of scheelite over wolframite. Altered magmatic titanite and hydrothermal titanite also show increased W and Mo concentrations due to interaction with and/or saturation from mineralizing fluids.

Basin inversion and structural architecture as constraints on fluid flow and Pb–Zn mineralization in the Paleo–Mesoproterozoic sedimentary sequences of northern Australia

As host to several world-class sediment-hosted Pb–Zn deposits and unknown quantities of conventional and unconventional gas, the variably inverted 1730–1640 Ma Calvert and 1640–1575 Ma Isa superbasins of northern Australia have been the subject of numerous seismic reflection studies with a view to better understanding basin architecture and fluid migration pathways. These studies reveal a structural architecture common to inverted sedimentary basins the world over, including much younger examples known to be prospective for oil and gas in the North Sea and elsewhere, with which they might be usefully compared. Such comparisons lend themselves to suggestions that the mineral and petroleum systems in Paleo–Mesoproterozoic northern Australia may have spatially, if not temporally overlapped and shared a common tectonic driver, consistent with the observation that basinal sequences hosting Pb–Zn mineralization in northern Australia are bituminous or abnormally enriched in hydrocarbons. Sediment-hosted Pb–Zn mineralization coeval with basin inversion first occurred during the 1650–1640 Ma Riversleigh Tectonic Event towards the close of the Calvert Superbasin with further pulses taking place during and subsequent to the onset of the 1620–1580 Ma Isa Orogeny and final closure of the Isa Superbasin. Mineralization is typically hosted by the post-rift or syn-inversion fraction of basin fill, contrary to existing interpretations of Pb–Zn ore genesis where the ore-forming fluids are introduced during the rifting or syn-extensional phase of basin development. Mineralizing fluids were instead expelled upwards during times of crustal shortening into structural and/or chemical traps developing in the hangingwalls of inverted normal faults. Inverted normal faults predominantly strike NNW and ENE, giving rise to a complex architecture of compartmentalized sub-basins whose individual uplifted basement blocks and doubly plunging periclinal folds exerted a strong control not only on the distribution and preservation of potential trap rocks but the direction of fluid flow, culminating in the co-location and trapping of mineralizing and hydrocarbon fluids in the same carbonaceous rocks. An important case study is the 1575 Ma Century Pb–Zn deposit where the carbonaceous host rocks served as both a reductant and basin seal during the influx of more oxidized mineralizing fluids, forcing the latter to give up their Pb and Zn metal. A transpressive tectonic regime in which basin inversion and mineralization were paired to folding, uplift, and erosion during arc–continent or continent–continent collision, and accompanied by orogen-parallel extensional collapse and strike-slip faulting best accounts for the observed relationships.