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Heather A. Lowers

Publications and source records attributed to Heather A. Lowers.

At least 37 records · Page 2Linked to original sources
USGS2024

Correlating quantified cathodoluminescence spectra in jadeite with micro-scale color measurements in visible-near infrared reflectance spectrometry

Cultures throughout history have valued jadeite jade (hereinafter jade), a natural material assemblage composed predominately of the NaAl endmember pyroxene, jadeite (NaAlSi 2 O 6 ) that is prized for its mechanical properties and enticing coloration [ 1 , 2 ]. The geological setting for the formation of jadeite-rich rocks and associated complex geochemical phenomena is well documented in the literature [ 3-5 ]. Unlike single crystal gems, jade often contains a mixture of colors, but the stone is perhaps best known for exhibiting a range of green hues from pale green to blue green, and to deep green [ 1 , 6 ]. Efforts to classify jade color include qualitative matching to a set of reference color tiles, and less commonly, use of a more quantitative set of color perception values first established by International Commission on Illumination’s (CIE 1931) color space, which includes values for light-dark luminance level (L*), a green-red vector (a*), and a blue-yellow vector (b*) [ 7 , 8 ]. Two principal mechanisms have been identified as the cause of green coloration in jadeite: 1) the chemical state of impurity Fe, either 2+ or 3+, and 2) minor to trace Cr in the crystal structure [ 9 , 10 ]. Previous studies have associated Cr 3+ with cathodoluminescence (CL) spectral features in jadeite using point spectrometry, with more recent connections made via 2D CL spectrum imaging [ 11-13 ]. In this effort, we are seeking to establish whether Cr impurities are correlated with green coloration in jadeite using micro-scale (≤110 μm) visible-near infrared (VIS-NIR) reflectance spectrometry.

Microscopy and Microanalysis↗
USGS2024

Cathodoluminescence imaging and spectrometry of a jadeite microbeam reference crystal: Detection of Ce3+

Options for selecting a high Na concentration mineral for instrument calibration that are suitably stable under the electron beam are limited [ 1 ]. NaCl (approximately a mass fraction of 39 % Na) is not practical for use alongside other embedded and polished materials in a mounted block of standards. While albite (NaAlSi 3 O 8 ; approximately a mass fraction of 8 % Na) represents a typical choice for some microanalysts, it may be subject to time dependent signal intensity issues, such as those observed for Na and other cations during analysis of hydrous glasses [ 2 ]. Near endmember jadeite pyroxene (NaAlSi 2 O 6 ; approximately mass fraction of 11 % Na) represents a desirable option for calibration given its relatively large concentration of Na and insensitivity to electron beam radiation with respect to X-ray output. Despite these desirable characteristics, jadeites have been shown to contain complex microstructures as the result of intracrystalline zoning [ 3 , 4 ], and the impact of chemical inhomogeneity within mineral standards and natural glasses has been documented [ 5-7 ]. In this study, a commercially obtained jadeite crystal (source location “China”) was studied to assess its microscale uniformity using a suite of microbeam methods, including dispersive red-green-blue multispectral cathodoluminescence imaging (CL RGB ), hyperspectral CL imaging spectrometry, energy dispersive X-ray spectrometry (EDS), SEM-based micro-X-ray fluorescence (μXRF), and wavelength dispersive X-ray spectrometry (WDS).

Microscopy and Microanalysis↗
USGS2024

In situ lung dust analysis by automated Field Emission Scanning Electron Microscopy with Energy Dispersive X-ray Spectroscopy: A method for assessing inorganic particles in tissue from coal miners

Context.— Overexposure to respirable coal mine dust can cause severe lung disease including progressive massive fibrosis (PMF). Field emission scanning electron microscopy with energy dispersive x-ray spectroscopy (FESEM-EDS) has been used for in situ lung dust particle analysis for evaluation of disease etiology. Automating such work can reduce time, costs, and user bias. Objective.— To develop and test an automated FESEM-EDS method for in situ analysis of inorganic particles in coal miner lung tissue. Design.— We programmed an automated FESEM-EDS procedure to collect particle size and elemental data, using lung tissue from 10 underground coal miners with PMF and 4 control cases. A statistical clustering approach was used to establish classification criteria based on particle chemistry. Data were correlated to PMF/non-PMF areas of the tissue, using corresponding brightfield microscopy images. Results for each miner case were compared with a separate corresponding analysis of particles recovered following tissue digestion. Results.— In situ analysis of miner tissues showed higher particle number densities than controls and densities were generally higher in PMF than non-PMF areas. Particle counts were typically dominated by aluminum silicates with varying percentages of silica. Compared to digestion results for the miner tissues, in situ results indicated lower density of particles (number per tissue volume), larger size, and a lower ratio of silica to total silicates—probably due to frequent particle clustering in situ. Conclusions.— Automated FESEM-EDS analysis of lung dust is feasible in situ and could be applied to a larger set of mineral dust–exposed lung tissues to investigate specific histologic features of PMF and other dust-related occupational diseases.

Archives of Pathology↗
USGS2024

Trace silicon determination in biological samples by inductively coupled plasma mass spectrometry (ICP-MS): Insight into volatility of silicon species in hydrofluoric acid digests for optimal sample preparation and introduction to ICP-MS

A method for the determination of trace levels of silicon from biological materials by inductively coupled plasma mass spectrometry (ICP-MS) has been developed. The volatility of water-soluble silicon species, hexafluorosilicic acid (H 2 SiF 6 ), and sodium metasilicate (Na 2 SiO 3 ) was investigated by evaporating respective solutions (50 µg/mL silicon) in nitric acid (HNO 3 ), nitric acid + hydrochloric acid (HNO 3 + HCl), and nitric acid + hydrochloric acid + hydrofluoric acid (HNO 3 + HCl + HF) at 120 °C on a hot-block to near dryness. The loss of silicon from H 2 SiF 6 solutions was substantial (>99%) regardless of the digestion medium. Losses were also substantial (>98%) for metasilicate solutions heated in HNO 3 + HCl + HF, while no significant loss occurred in HNO 3 or HNO 3 + HCl. These results show that H 2 SiF 6 species were highly volatile and potential losses could confound accuracy at trace level determinations by ICP-MS if digestates prepared in HF are heated to eliminate HF. Among the various matrices comprising major elements, sodium appeared to be effective in reducing silicon loss from H 2 SiF 6 solutions. Excess sodium chloride (NaCl) matrix provided better stability, improving silicon recoveries by up to about 80% in evaporated HF digestates of soil and mine waste samples, but losses could not be fully prevented. To safely remove excess acids and circumvent the adverse effects of excess HF (e.g., risk of high Si background signals), a two-step digestion scheme was adopted for the preparation of biological samples containing trace silicon levels. A closed-vessel digestion was performed either in 4 mL of concentrated HNO 3 and 1 mL of concentrated HCl or 4 mL of concentrated HNO 3 , 1 mL of concentrated HCl and 1 mL of concentrated HClO 4 on a hot plate at 140 °C. Digestates were then evaporated to incipient dryness at 120 °C to remove the acids. A second closed-vessel digestion was carried out to dissolve silicates in 0.5 mL of concentrated HNO 3 and 0.5 mL of concentrated HF at 130 °C. After digestion, digestates were diluted to 10 mL. The solution containing about 5% HNO 3 and 5% HF was directly analyzed by ICP-MS equipped with an HF-inert sample introduction system. The limit of detection was about 110 µg/L for 28 Si when using the Kinetic Energy Discrimination (KED) mode. The method was used to determine silicon in various plant and tissue certified reference materials. Data were acquired for 28 Si using KED and standard (STD) modes, and 74 Ge and 103 Rh as internal standard elements. There was not any significant difference between the accuracy and precision of the results obtained with 74 Ge and 103 Rh within the same measurement mode. Precision, calculated as relative standard deviation for four replicate analyses, varied from 5.3 (tomato leaves) to 21% (peach leaves) for plant and from 2.2 (oyster tissue) to 33% (bovine liver) for tissue SRM/CRMs. Poor precision was attributed to material heterogeneity and the large particle size distribution. An analysis of lung tissue samples from those with occupational exposure to silica dust revealed that tissues possessed substantial levels of water-soluble silicates, but the most silicon was present in the particulate matter fraction.

Minerals↗
USGS2024

Paleoproterozoic reworking of Archean crust and extreme back-arc metamorphism in the enigmatic southern Trans-Hudson orogen

The crustal evolution of the southernmost ∼2000–1800 Ma Trans-Hudson orogen (THO) is enigmatic due to burial by Phanerozoic sediments. We provide new insights through petrochronologic analysis of a paragneiss drill core sample. Detrital zircon age peaks at 2625, 2340, and 1880 Ma and Hf isotopes suggest Paleoproterozoic arc development proximal to Archean source(s). Phase equilibria modeling and ternary feldspar thermometry suggest peak conditions of ≥1 GPa, ≥900°C, the first recognition of extreme, ultra-high temperature metamorphism in the THO. The largely isobaric P-T path, rapid heating rate, and ∼20 Myr duration (1872–1850 Ma) of peak conditions suggest that this metamorphism occurred in a back-arc tectonic setting. The sample records post-peak (1850–1815 Ma) mid-crustal residence, slow cooling, and exhumation. Further retrogression occurred during Proterozoic regional exhumation (1630–1470 Ma) and Phanerozoic (360–220 Ma) reheating and/or fluid influx. Evidence for Paleoproterozoic arc(s) supports geophysical data for Archean cratonic and Paleoproterozoic arc crust in this region.

Geophysical Research Letters↗
USGS2024

Particle morphology and elemental analysis of lung tissue from post-9/11 military personnel with biopsy-proven lung disease

The relationship between exposure to inhaled inorganic particulate matter and risk for deployment-related lung disease in military personnel is unclear due in part to difficulties characterizing individual exposure to airborne hazards. We evaluated the association between self-reported deployment exposures and particulate matter (PM) contained in lung tissue from previously deployed personnel with lung disease (“deployers”). The PM in deployer tissues was compared to normal lung tissue PM using the analytical results of scanning electron microscopy and inductively coupled plasma mass spectrometry. The majority of PM phases for both the deployers and the controls were sub-micrometer in size and were compositionally classified as aluminum and zirconium oxides, carbonaceous particles, iron oxides, titanium oxides, silica, other silicates, and other metals. The proportion of silica and other silicates was significantly higher in the retained dust from military veterans with biopsy-confirmed deployment-related lung disease compared to the control subjects. Within the deployer population, those who had combat jobs had a higher total PM burden, though the difference was not statistically significant. These findings have important implications for understanding the role of inhaled inorganic dusts in the risk for lung injury in previously deployed military veterans.

International Journal of Enviornmental Research an↗
USGS2023

Hydrothermal monazite and xenotime chemistry as genetic discriminators for intrusion-related and orogenic gold deposits: Implications for an orogenic origin of the Pogo gold deposit, Alaska

Attempts to geochemically distinguish between metamorphic-hydrothermal systems that form orogenic gold deposits and both reduced and oxidized magmatic-hydrothermal systems using isotopes or metal associations have proven ambiguous, particularly for orogenic gold and reduced intrusion-related gold systems. The absence of conclusive geochemical discriminators and the overlap in geologic characteristics have led to gold deposit models being potentially incorrectly applied, which in turn negatively affect regional mineral exploration and mine planning. In this study, in situ electron microprobe geochemical analyses of hydrothermal monazite and xenotime crystals associated with different types of gold-bearing deposits are shown to be effective geochemical discriminators. There are notable differences in mineral chemistry such as rare earth element (REE) profiles, total light REE, Dy, Er, Pr, Y, Nd/Sm, and La/Sm that distinguish monazite precipitated from metamorphic-hydrothermal fluids that form orogenic gold deposits and those precipitated from magmatic-hydrothermal fluids that form both porphyry Cu-Mo-Au and reduced intrusion-related gold deposits. Notable differences in overall xenotime abundances and concentrations of heavy REEs, Ca, and Sc are distinctive between the different deposit classes for xenotime. The origin of the controversially classified Pogo gold deposit, Tintina gold province, Alaska, which has been characterized as both a reduced intrusion-related and an orogenic gold deposit, is tested based upon the noted chemical differences associated with these hydrothermal phosphates. The findings of this study have implications for exploration and mine development in the Tintina gold province and other areas that contain deposits that are controversially classified as either orogenic or as magmatic-hydrothermal gold deposits.

Alaska↗
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

Monazite and xenotime petrochronologic constraints on four Proterozoic tectonic episodes and ca. 1705 Ma age of the Uncompahgre Formation, southwestern Colorado, USA

The Proterozoic tectonic evolution of the south-western USA remains incompletely understood due to limited constraints on the timing and conditions of the tectono-metamorphic phases and depositional age of metasedimentary successions. We integrated multi-scale compositional mapping, petrologic modeling, and in situ geochronology to constrain pressure-temperature-time paths from samples of Paleoproterozoic basement gneisses and overlying quartzites in southwestern Colorado, USA. Basement gneiss from the western Needle Mountains records metamorphic conditions of 600 °C at 0.75 GPa at 1764 ± 9 Ma and ~575 °C at 1741 ± 10 Ma. Gneiss sampled from drill core near Pagosa Springs, Colorado, records conditions of 700 °C at 1748 ± 9 Ma, 800 °C at 1.1 GPa at 1650 ± 40 Ma, 540 °C at 1570 ± 36 Ma, and 440 °C at 1424 ± 12 Ma. The Uncompahgre Formation was deposited at ca. 1705 Ma, as constrained by detrital monazite (1707 ± 8 Ma) and xenotime (1692 ± 40, 1725 ± 50 Ma), metamorphic xenotime (1650 ± 10 Ma), and published 40 Ar/ 39 Ar and detrital zircon data. Compositions of ca. 1705 Ma detrital monazite and xenotime are consistent with derivation from a garnet-bearing source in the Yavapai orogenic hinterland. The Vallecito Conglomerate and Uncompahgre Formation record macroscopic folding and greenschist-facies metamorphism at 1650 ± 10 Ma and temperatures of 270 °C to >570 °C at 1470–1400 Ma. Laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) zircon geochronology yielded dates of 1775 ± 18 Ma from the Twilight Gneiss and 1696 ± 7 Ma from the Bakers Bridge Granite, supporting previous isotope dilution–thermal ionization mass spectrometry (ID-TIMS) dates. The Eolus Granite yielded a date of 1463 ± 6 Ma, which is older than previous 1.44–1.43 Ga ID-TIMS dates. The newly dated granite of Cataract Gulch is 1421 ± 12 Ma. In situ analysis of detrital and metamorphic monazite and xenotime, igneous zircon, and quantitative thermobarometry, integrated with previously published constraints, indicate multiple tectonic episodes after the emplacement of 1800–1760 Ma arc-related rocks. The region experienced greenschist- to amphibolite-facies metamorphism (M1) from 1760 Ma to 1740 Ma, which was followed by the intrusion of granites at 1730–1695 Ma and deposition of the Uncompahgre Formation at ca. 1705 Ma, contemporaneous with the Yavapai orogeny. Metamorphism at 1680–1600 Ma was characterized by greenschist-facies conditions near Ouray, Colorado, and granulite-facies conditions near Pagosa Springs (M2) during the Mazatzal orogeny. From 1470 Ma to 1400 Ma, greenschist- to amphibolite-facies metamorphism (M3) and largely granitic plutonism occurred during the protracted Picuris orogeny. These results demonstrate the power of monazite and xenotime analyses to constrain depositional ages, provenance, and pressure-temperature-time ( P - T - t ) paths to resolve the compound orogenic history that is characteristic of most mountain belts.

Colorado↗
USGS2023

Characterizing lung particulates using quantitative microscopy in coal miners with severe pneumoconiosis

Context.— Current approaches for characterizing retained lung dust using pathologists' qualitative assessment or scanning electron microscopy with energy-dispersive spectroscopy (SEM/EDS) have limitations. Objective.— To explore polarized light microscopy coupled with image-processing software, termed quantitative microscopy–particulate matter (QM-PM), as a tool to characterize in situ dust in lung tissue of US coal miners with progressive massive fibrosis. Design.— We developed a standardized protocol using microscopy images to characterize the in situ burden of birefringent crystalline silica/silicate particles (mineral density) and carbonaceous particles (pigment fraction). Mineral density and pigment fraction were compared with pathologists' qualitative assessments and SEM/EDS analyses. Particle features were compared between historical (born before 1930) and contemporary coal miners, who likely had different exposures following changes in mining technology. Results.— Lung tissue samples from 85 coal miners (62 historical and 23 contemporary) and 10 healthy controls were analyzed using QM-PM. Mineral density and pigment fraction measurements with QM-PM were comparable to consensus pathologists' scoring and SEM/EDS analyses. Contemporary miners had greater mineral density than historical miners (186 456 versus 63 727/mm 3 ; P = .02) and controls (4542/mm 3 ), consistent with higher amounts of silica/silicate dust. Contemporary and historical miners had similar particle sizes (median area, 1.00 versus 1.14 μm 2 ; P = .46) and birefringence under polarized light (median grayscale brightness: 80.9 versus 87.6; P = .29). Conclusions.— QM-PM reliably characterizes in situ silica/silicate and carbonaceous particles in a reproducible, automated, accessible, and time/cost/labor-efficient manner, and shows promise as a tool for understanding occupational lung pathology and targeting exposure controls.

Archives of Pathology and Laboratory Medicine↗
USGS2023

Reconnaissance mineral and cathodoluminescence studies of gold occurrences in the Pogo-Black Mountain area, eastern interior Alaska, USA

The Pogo Au deposit is the largest of a number of gold occurrences in eastern interior Alaska, that occur along a broad trend from west of Pogo to Black Mountain. Some of these occurrences are hosted in amphibolite facies gneisses and others in mid-Cretaceous igneous rocks that intruded the older metamorphic rocks. All occurrences contain arsenopyrite and pyrite. Whole rock geochemical trends distinguish most metamorphic rock-hosted vein prospects (strong Bi-Te-Au correlations) and intrusion-hosted occurrences (weak As-Au correlations). Brecciated quartz veins in metamorphic rocks have paragentically late Bi-Te (±S) + Au that post-dates Fe-As sulphide deposition. High grade vein samples from the Tibbs Creek intrusion-hosted deposits contain pyrite and arsenopyrite, generally lack Bi-Te minerals, but can contain paragentically younger euhedral quartz, stibnite and carbonate. Cathodoluminescence studies of gold-rich samples indicate that quartz dissolution occurred during the syn- to post-tectonic Bi-Te-Au deposition, and the later stibnite event. In the case of metamorphic rock-hosted deposits (e.g., Pogo, Gray Lead), Bi-Te and gold deposition commonly occurs in microfractures within quartz veins; the limited quartz in these fractures have distinctive CL response. We propose that gold deposition is related to changes in P-T conditions rather than fluid-rock chemical reactions. Similar quartz dissolution textures affect the void-filling euhedral quartz before or during stibnite and carbonate mineralization in the high-grade Au samples from Blue Lead.

Alaska↗
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↗
USGS2022

Formation of orogenic gold deposits by progressive movement of a fault-fracture mesh through the upper crustal brittle-ductile transition zone

Orogenic gold deposits are comprised of complex quartz vein arrays that form as a result of fluid flow along transcrustal fault zones in active orogenic belts. Mineral precipitation in these deposits occurs under variable pressure conditions, but a mechanism explaining how the pressure regimes evolve through time has not previously been proposed. Here we show that extensional quartz veins at the Garrcon deposit in the Abitibi greenstone belt of Canada preserve petrographic characteristics suggesting that the three recognized paragenetic stages formed within different pressure regimes. The first stage involved the growth of interlocking quartz grains competing for space in fractures held open by hydrothermal fluids at supralithostatic pressures. Subsequent fluid flow at fluctuating pressure conditions caused recrystallization of the vein quartz and the precipitation of sulfide minerals through wall-rock sulfidation, with some of the sulfide minerals containing microscopic gold. These pressure fluctuations between supralithostatic to near-hydrostatic conditions resulted in the post-entrapment modification of the fluid inclusion inventory of the quartz. Late fluid flow occurred at near-hydrostatic conditions and resulted in the formation of fluid inclusions that have not been affected by post-entrapment modification as pressure conditions never returned to supralithostatic conditions. This late fluid flow is interpreted to have formed the texturally late, coarse native gold that occurs along quartz grain boundaries and in open spaces. The systematic evolution of the pressure regimes in orogenic gold deposits such as Garrcon can be explained by relative movement of fault-fracture meshes across the base of the upper crustal brittle-ductile transition zone. We conclude that early vein quartz in orogenic deposits is precipitated at near-lithostatic conditions whereas the paragenetically late gold is introduced at distinctly lower pressure.

Scientific Reports↗
USGS2022

Cathodoluminescence response of barite at room and liquid nitrogen temperatures

Rare earth element (REE) enrichment in the Elk Creek carbonatite, Nebraska USA, is comparable to ore grade enrichment in carbonatite-hosted REE deposits[1]. Petrographic examination of textures documents a complex history of crystallization, brecciation, recrystallization, oxidation, and near surface alteration. Barite (BaSO 4 ) is present in most units, including REE-enriched zones, such that it may provide important constraints on processes that lead to ore-grade enrichment of carbonatites. Samples containing barite from different temperature regimes within the deposit were chosen to study the cathodoluminescence (CL) response at room and liquid nitrogen (LN) temperatures to help determine the processes by which REEs were enriched within the deposit and possible contributions of REE to the CL response.

Conference Paper↗
USGS2022

The geochemical and textural transition between the Reef Package and its hanging wall, Stillwater Complex, Montana, USA

The highest grade Pd-Pt deposit on Earth, the J-M Reef, is hosted in coarse-grained to pegmatoidal cumulates called the Reef Package. Decades of mine development of the J-M Reef have revealed that a distinct discontinuity in rock fabric marks the top of the rock unit that hosts economic-grade sulfide mineralization. Mine geologists refer to this discontinuity as the hanging wall contact. This contact is the top of the Reef Package and is always locatable—either by the change in rock fabric or by distinctive hanging wall textures of silicate minerals—even when the reef sulfide mineralization is absent. This rather subtle textural feature is used reliably by mine geologists to follow the Reef during exploration and mine development. Although some high tenor sulfides (>1000 ppm Pd in 100% sulfide) are found sporadically in the hanging wall cumulates, these accumulations are too small to be economically viable. We present quantitative rock fabric data for four Reef Package and hanging wall intersections collected by electron back-scattered diffraction (EBSD). Plagioclase fabrics in the hanging wall are characterized by low variance in grain sizes and a strong point maximum concentration of (010) and a perpendicular girdle distribution of [100] consistent with an axial B-type fabric. These fabrics are indicative of either compaction of the crystal mush or crystal settling of nucleated crystals, the bulk magma in a chamber. Conversely, the fabrics of the Reef Package show higher variance grain in size distributions and weak to undeveloped preferred orientation of plagioclase crystals that did not undergo significant alignment or textural equilibration of plagioclase grains. The absence of foliation in the Reef Package stands in contrast both to hanging wall fabrics and to other reported EBSD datasets of plagioclase crystals orientations from the Bushveld Complex, the Skaergaard Intrusion, and the Rum Intrusion. Furthermore, plagioclase crystal size distributions for the Reef Package show flatter slopes and convex profiles with fewer crystals at small size fractions indicating the dissolution of small crystals during partial melting and textural coarsening (i.e . Ostwald ripening) and crystal growth. Crystal growth was favored over the nucleation of new crystals during prolonged interaction with a hot infiltrating melt into the resident mush resulting in the coarse-grained textures of the Reef Package cumulates. The hanging wall contact represents a boundary between partially remelted crystal mush of the Reef Package, where sulfide mineralization formed and accumulated, and an overlying essentially barren cumulate pile. The hanging wall cumulates formed following the cessation of footwall erosion and the resumption of crystal accumulation by normal magma chamber processes.

Montana↗
USGS2022

The dynamic floor of Yellowstone Lake, Wyoming, USA: The last 14 k.y. of hydrothermal explosions, venting, doming, and faulting

Hydrothermal explosions are significant potential hazards in Yellowstone National Park, Wyoming, USA. The northern Yellowstone Lake area hosts the three largest hydrothermal explosion craters known on Earth empowered by the highest heat flow values in Yellowstone and active seismicity and deformation. Geological and geochemical studies of eighteen sublacustrine cores provide the first detailed synthesis of the age, sedimentary facies, and origin of multiple hydrothermal explosion deposits. New tephrochronology and radiocarbon results provide a four-dimensional view of recent geologic activity since recession at ca. 15–14.5 ka of the >1-km-thick Pinedale ice sheet. The sedimentary record in Yellowstone Lake contains multiple hydrothermal explosion deposits ranging in age from ca. 13 ka to ~1860 CE. Hydrothermal explosions require a sudden drop in pressure resulting in rapid expansion of high-temperature fluids causing fragmentation, ejection, and crater formation; explosions may be initiated by seismicity, faulting, deformation, or rapid lake-level changes. Fallout and transport of ejecta produces distinct facies of subaqueous hydrothermal explosion deposits. Yellowstone hydrothermal systems are characterized by alkaline-Cl and/or vapor-dominated fluids that, respectively, produce alteration dominated by silica-smectite-chlorite or by kaolinite. Alkaline-Cl liquids flash to steam during hydrothermal explosions, producing much more energetic events than simple vapor expansion in vapor-dominated systems. Two enormous explosion events in Yellowstone Lake were triggered quite differently: Elliott’s Crater explosion resulted from a major seismic event (8 ka) that ruptured an impervious hydrothermal dome, whereas the Mary Bay explosion (13 ka) was triggered by a sudden drop in lake level stimulated by a seismic event, tsunami, and outlet channel erosion.

Wyoming↗