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Recrystallized Impact Glasses of the Onaping Formation and the Sudbury Igneous Complex, Sudbury Structure, Ontario, Canada

The origin of the Sudbury Structure and of the associated heterolithic breccias of the Onaping Formation and the Sudbury Igneous Complex have been controversial. While an impact origin of the structure has gained wide acceptance over the last 15 years, the origin of the recrystallized Onaping Formation glasses and of the igneous complex is still being debated. Recently the interpretation of the breccias of the Onaping Formation as suevitic fall-back impact breccias has been challenged. The igneous complex is interpreted either as a differentiated impact melt sheet or as a combination of an upper impact melt represented by the granophyre, and a lower, impact-triggered magmatic body consisting of the norite-sublayer formations. The Onaping Formation contains glasses as fluidal and nonfluidal fragments of various shapes and sizes. They are recrystallized, and our research indicates that they are petrographically heterogeneous and span a wide range of chemical compositions. These characteristics are not known from glasses of volcanic deposits. This suggests an origin by shock vitrification, an interpretation consistent with their association with numerous and varied country rock clasts that exhibit microscopic shock metamorphic features. The recrystallized glass fragments represent individual solid-state and liquid-state vitrified rocks or relatively small melt pods. The basal member lies beneath the Gray and Black members of the Onaping Formation and, where not metamorphic, has an igneous matrix. Igneous-textured melt bodies occur in the upper two members and above the Basal Member. A comparison of the chemical compositions of recrystallized glasses and of the matrices of the Basal Member and the melt bodies with the components and the bulk composition of the igneous complex is inconclusive as to the origin of the igneous complex. Basal Member matrix and Melt Bodies, on average, are chemically similar to the granophyre of the Sudbury Igneous Complex, suggesting that they are genetically related. Our chemical results allow interpretation of the entire igneous complex as a differentiated impact melt. However, they are also consistent with the granophyre alone being the impact melt and the nofite and quartz gabbro beneath it representing an impact-triggered magmatic body. This interpretation is preferred, as it is consistent with a number of field observations. A re-evaluation and extension of structural field studies and of geochemical data, as well as a systematic study of the contact relationships of the various igneous phases of the igneous complex, are needed to establish a Sudbury impact model consistent with all data and observations

Dressler, B. O.↗

A Model for Siderophile Element Distribution in Planetary Differentiation

Planetary differentiation begins with partial melting of small planetesimals. At low degrees of partial melting, a sulfur-rich liquid segregates by physical mechanisms including deformation-assisted porous flow. Experimental studies of the physical mechanisms by which Fe-S melts segregate from the silicate matrix of a molten H chondrite are part of a companion paper. Geochemical studies of these experimental products revealed that metallic liquids were in equilibrium with residual metal in the H chondrite matrix. This contribution explores the geochemical signatures produced by early stages of core formation. Particularly, low-degree partial melt segregation of Fe-S liquids leaves residual metal in the silicate matrix. Some achondrites appear to be residues of partial melting, e.g., ureilites, which are known to contain metal. The metal in these achondrites may show a distinct elemental signature. To quantify the effect of sulfur on siderophile element contents of residual metal we have developed a model based on recent parametrizations of equilibrium solid metal-liquid metal partitioning experiments.

Humayun, M.↗

Highland crust at the Apollo 14 site: A review

Recent petrologic studies of pristine nonmare samples from the Apollo 14 site have demonstrated the unique character of the western highlands crust. Many of the lithologies which occur here are not found at other highland sites or represent unique variations of more common lithologies. Rare highland samples found at the Apollo 12 site have petrologic and geochemical affinities with the Apollo 14 highland suite and the two sites taken together constitute what can be called the Western Highland Province. Rocks of the Western Highland Province are geochemically distinct from similar lithologies found at eastern highland sites (Apollo 15, Apollo 16, Apollo 17, and the Luna sites) -- a fact which adds further complications to current petrogenetic models for the lunar crust. Nonetheless, an understanding of how the Western Highlands Province formed and why it differs from highland crust in the east is crucial to our overall understanding of primordial lunar differentiation and petrogenesis.

Shervais, John W.↗

The western highland province at the Apollo 14 site

Recent petrologic studies of pristine nonmare samples from the Apollo 14 site have demonstrated the unique character of the western highlands crust. Many of the lithologies which occur here are not found at other highland sites or represent unique variations of more common lithologies. Rare highland samples found at the Apollo 12 site have petrologic and geochemical affinities with the Apollo 14 highland suite, and the two sites taken together constitute what can be called the Western Highland Province. Rocks of the Western Highland Province are geochemically distinct from similar lithologies found at eastern highland sites (Apollo 15, Apollo 16, Apollo 17, and the Luna sites)--a fact which adds further complications to current petrogenetic models for the lunar crust. Nonetheless, and understanding of how the Western Highlands Province formed and why it differs from highland crust in the east is crucial to our overall understanding of primordial lunar differentiation and petrogenesis.

Shervais, John W.↗

Interpretable Machine Learning Models for Autonomous Characterization of Analogue Ocean World Seawater Chemistry and Biosignature Potential Using Isotope Ratio Data

Background: Future missions to ocean worlds, such as Enceladus and Europa, will attempt to characterize the subsurface seawater chemistry and assess the potential for life. Such missions will be equipped with capabilities to precisely measure volatile isotopes in plumes, atmospheres, and exospheres. Motivation: While large isotopic fractionations can indicate a biological source, there are signatures resulting from abiotic geochemical processes that mimic isotopic biosignatures. While machine learning (ML) has the potential to disentangle competing effects and biotic mimicry, high-dimensional isotope ratio mass spectrometry (IRMS) data is likely to contain noise/irrelevant features and involve complex statistical interactions that make human inference and interpretation difficult. Further, ML predictions with as far-reaching implications as an extraterrestrial biosignature on an ocean world requires the use of interpretable models (i.e., not “black box” models) with physically and mathematically meaningful feature spaces along with false positive diagnostics. Methods: We use volatile CO2 IRMS data of analogue ocean world seawaters to validate an ML approach to provide biogeochemical context for biosignature detection. We employ a feature selection method called nearest-neighbor projected distance regression (NPDR) that detects statistical interactions and helps elucidate the mechanisms of the Random Forest classification models. Results: We train and validate predictive ML models on volatile CO2 IRMS data of analogue ocean world seawaters to predict major salt components (e.g., MgSO4, NaHCO3), pH, ionic strength, and the presence of biosignatures. Features derived from IRMS measurements are augmented with extracted time-series features. Our results show high test accuracy and interpretability, which is increased by interaction network visualization, sample-wise variable importance scores, and single-sample class probability estimates. We demonstrate an ML mission software solution that triggers autonomous data transmission and biogeochemical sample prediction.

geochemistry↗

The temperature gradient in the solar nebula

The available compositional data on planets and satellites can be used to place stringent limits on the thermal environment in the solar nebula. The densities of the terrestrial planets, Ceres and Vesta, the Galilean satellites, and Titan; the atmospheric compositions of several of these bodies; and geochemical and geophysical data on the earth combine to define a strong dependence of formation temperature on heliocentric distance. It is impossible to reconcile the available compositional data with any model in which the formation temperatures of these bodies are determined by radiative equilibrium with the sun, regardless of the sun's luminosity. Rather, the data support Cameron's hypothesis of a dense, convective solar nebula, opaque to solar radiation, with an adiabatic temperature-pressure profile.

Lewis, J. S.↗

Acquisition of a Gas Chromatograph/Mass Spectrometer System for Laboratory Study of Prebiotic Organic Geochemical Processes on the Early Earth, Mars, and Meteorites

This was a major equipment grant that provided funds ($72K) for purchase of a benchtop gas chromatograph-mass spectrometer (GC-MS) for use in experimental studies of prebiotic organic compounds. An Agilent model 689015973 GC-MS was purchased and installed in the PI's lab in August of 2003. The instrument is now being used for a variety of research projects. The primary use of the instrument is to analyze and quantify organic products of laboratory experiments conducted by the PI. One example is shown, which shows organic products (predominantly n-alkanes) formed during Fischer-Tropsch-type abiotic synthesis under hydrothermal conditions. The analytical capabilities of the GC- MS allowed identification of the numerous organic products of this as well as other laboratory experiments. A key use of the instrument in this research is that the mass spectrometer capabilities allow use of isotopically labeled reactants to trace the progress of reactions and evaluate background contaminants. collaborative projects with other scientists involved in exobiology & astrobiology research (e.g., Mitch Schulte, NASA Ames; Katrina Edwards, Woods Hole Oceanographic Institution). For instance, an analysis of membrane lipids of an lithoautotrophic iron-oxidizing bacteria being grown on basalt as a source of metabolic energy, a project where the instrument is being used to evaluate possible biomarker compounds from these organisms is shown. These iron oxidizers are thought to be similar to those living within the ocean crust, and are being investigated as possible analog organisms to those on the early Earth or crust of Mars. The instrument has also been used by an outside investigator (graduate student Brandon Canfeld, Arizona State University) for identification and isotopic characterization of experimental products of abiotic organic synthesis experiments he is conducting with Dr. John Holloway. analysis of quality control samples for other NASA-funded projects. For instance, an analysis of residual hydrocarbon contaminants on the internal surface of the shell of an atmospheric sounding rocket is shown. This analysis was used to help determine the source of the contaminating compounds. In the future, the instrument will continue to be used for quality control analysis in clean rooms and instrument construction facilities within the Laboratory for Atmospheric and Space Physics, where the GC-MS is housed.

McCollom, Thomas↗

Thermal evolutions of the terrestrial planets

Theoretical models are formulated for the thermal evolution of the moon, Mercury, Mars, Venus, and hypothetical minor planets, with consideration of conduction, solid-state convection, and differentiation. A variety of geological, geochemical and geophysical data is used to constrain both the present-day temperatures and the thermal histories of the planetary interiors. The data imply that the planets were heated during or shortly after formation and that all the terrestrial planets started differentiating early in their history. The size of the planet is the primary factor in determining its present-day thermal state. A planetary body with radius less than 1000 km is unlikely to reach melting, given heat source concentrations similar to terrestrial values and in the absence of intensive early heating.

Toksoz, M. N.↗

Thermal regimes in impact melts and the petrology of the Apollo 17 Station 6 boulder

A progress report is presented on the petrologic study of the Station 6 boulder, taking into account the implications of its petrographic and geochemical studies to the understanding of the processes of formation and crystallization of impact melts. The interpretation of the data from the boulder suggests processes that appear reasonable for a petrogenetic model of impact events large enough to produce a layer of melt a kilometer or more wide and at most a few tens of meters thick. A summary of the model is presented. The primary difference between the new model and the previous models of Warner et al. (1973, 1974) and Simonds et al. (1973, 1974) is that melt and clasts are derived from distinctly different parts of the cratering regime. The cooling is modeled in two steps, first the rapid equilibration between clasts and matrix, and second, the much slower loss of heat to the surroundings.

Simonds, C. H.↗

Lunar and Planetary Science Conference, 16th, Houston, TX, March 11-15, 1985, Proceedings. Part 1

Various papers on lunar studies, meteorites and cosmic dust, Mars, and tektites are presented. The topics discussed include: very high potassium basalt; complications in mare basalt petrogenesis; mare basalt genesis; modeling trace elements and isotopic ratios; Zr-Hf-Ta fractionation during lunar evolution; petrology of the Apollo 12 highland component; petrologic province maps of the lunar highlands derived from orbital geochemical data; petrology and chemistry of Apollo 12 regolith breccias; chemical variability and origin of agglutinitic glass; multistage exposure history of the 74261 soil constituents; and an experimental investigation of agglutinate melting mechanisms; shocked mixtures of sodium and potassium feldspars. Also addressed are: cooling history of some Antarctic ureilites; the Leoville accretionary breccia; ubiquitous brecciation after metamorphism in equilibrated ordinary chondrites; layer silicates in a chondritic porous interplanetary dust particle; estimates of rheological properties for flows on the Martian volcano Ascraeus Mons; the Martian dust storm of Sol 1742; and late Eocene North American microtektites and clinopyroxene-bearing spherules.

Ryder, G.↗

Lunar and Planetary Science XXXV: Impacts: Observations and Experiments

The title in this section include: 1) Impactites of the Haughton Impact Structure, Devon Island, Nunavut, Canada; 2) Geochemical Characteristics of Impactites from the Yaxcopoil-1 ICDP Drill Core, Chicxulub Impact Structure, Mexico; 3) Investigation of the Ries Impact Crater Based upon Old and New Geophysical Data and Numerical Modeling; 4) Potential of Radar Imaging and Sounding Methods in Mapping Heavily Eroded Impact Craters: Mapping Some Structural Elements of the Hico Crater, TX; 5) From Simple to Complex Craters: The Mechanics of Late-time Crater Adjustments; 6) Impact Structures: What Does Crater Diameter Mean? 7) Early-Time Temperature Evolution of the Impact Flash and Beyond; 8) Probing Impact-Generated Vapor Plumes; 9) Non-Ballistic Vapor-Driven Ejecta; 10) Depth and Diameter of Transient Craters; 11) A Plausibility of Z-Model; 12) Experiments with Explosives and Ordnance Disposal Devices for the Simulation of Specific Processes During Shallow-Marine Impacts; 13) Collisional Fragmentation of Rotating Bodies.

Source record↗

The Long-Term Evolution of the Atmosphere of Venus: Processes and Feedback Mechanisms

This work reviews the long-term evolution of the atmosphere of Venus, and modulation of its composition by interior/exterior cycling. The formation and evolution of Venus’s atmosphere, leading to contemporary surface conditions, remain hotly debated topics, and involve questions that tie into many disciplines. We explore these various inter-related mechanisms which shaped the evolution of the atmosphere, starting with the volatile sources and sinks. Going from the deep interior to the top of the atmosphere, we describe volcanic out-gassing, surface-atmosphere interactions, and atmosphere escape. Furthermore, we address more complex aspects of the history of Venus, including the role of Late Accretion impacts, how magnetic field generation is tied into long-term evolution, and the implications of geochemical and geodynamical feedback cycles for atmospheric evolution. We highlight plausible end-member evolutionary pathways that Venus could have followed, from accretion to its present-day state, based on modeling and observations. In a first scenario, the planet was desiccated by atmospheric escape during the magma ocean phase. In a second scenario, Venus could have harbored surface liquid water for long periods of time, until its temperate climate was destabilized and it entered a runaway greenhouse phase. In a third scenario, Venus’s inefficient outgassing could have kept water inside the planet, where hy- drogen was trapped in the core and the mantle was oxidized. We discuss existing evidence and future observations/missions required to refine our understanding of the planet’s history and of the complex feedback cycles between the interior, surface, and atmosphere that have been operating in the past, present or future of Venus.

Venus↗

Modeling 238U/204Pb (μ) and Initial Pb of Lunar Meteorite Northwest Africa 12593

Apatite Ca 5 (PO 4 ) 3 (F, Cl, OH) serves as a valuable analytical resource. It is the only nominally hydrous phase on the moon and possesses the capacity to concentrate elements like U, Th, Pb, and rare earth elements (REE). This characteristic facilitates its use in U-Pb and Pb-Pb geochronology, allowing for the determination of the initial isotopic Pb and the -238 U/ -204 Pb ratio (μ) of the parent melt. In situ analysis of apatite grains can provide a detailed record of geochemical changes, revealing the broader petrogenetic and volatile history of the source material. This mineral is particularly informative in understanding the developmental history of its source. In situ analyses are crucial for lunar samples, predominantly composed of breccias, where correlating distinct grains with whole rock analyses poses challenges. This study utilizes in situ apatite isotopic analysis of apatite grains in lunar meteorite Northwest Africa 12593 and model the initial Pb isotopic composition and -238 U/ -204 Pb (μ) of the source. We present in situ Secondary Ionization Mass Spectrometry (SIMS) Pb-Pb analyses of 12 apatite grains in Northwest Africa (NWA) 12593 to test two hypotheses: 1) NWA 12593 clasts and matrix are closely related and from the same source, and 2) the matrix material previously documented as having a highland affinity has a lower modeled μ then KREEP.

K M Lehman Franco↗

Apollo 15 mare basalts: A diverse suite or two distinct groups?

The literature geochemical data for 60 Apollo 15 mare basalts were compiled in order to evaluate possible intra-group relationships of the Apollo 15 mare basalts. The effects of olivine or pigeonite fractionation were discussed. Models were developed to explain the trace element characteristics of the samples.

Salpas, P. A.↗

Static Wind Tunnel Testing of a Legged Venus Lander

A static wind tunnel test was conducted to determine the static aerodynamic coe cients of the surface lander design proposed by the Venus In-Situ Atmospheric and Geochemical Explorer (VISAGE). The baseline design of the lander consists of a spherical pressure vessel with a top-mounted circular drag plate for aerodynamic deceleration, and three xed landing legs. A modular subscale lander model, which allowed testing of several drag plate and landing leg con gurations, was fabricated using rapid-prototyping techniques. The model was tested with four di erent drag plates and three di erent leg con gurations, at a dynamic pressure of 1610 Pa and Mach number of 0.15. Testing was conducted using legs of varying diameter in order to determine the appropriate scaling of the results to Reynolds numbers representative of terminal descent at Venus. The static aerodynamic force (axial, normal, and side), and moment (rolling, pitching, yawing) coe cients for each lander con guration were determined as a function of model orientation. All model con gurations were found to be statically stable in the range of total angles of attack considered (0 to 30 deg). However, the drag performance and degree of static stability of the model were dependent on the dihedral angle of the circular drag plate. The results will enable the creation of a preliminary aerodatabase for the VISAGE lander concept, and allow the e ect of design changes on aerodynamic performance to be evaluated.

Rabinovitch, Jason↗

Chemical and Thermodynamic Constraints on the Thermal Evolution of Eucrites

Vesta is the only differentiated asteroid with a nearly intact crust, making it the candidate for studying early planetary differentiation. It is commonly thought that the howardite, eucrite, and diogenite (HED) clan of meteorites derive from Vesta, and thus the study of HEDs is important for understanding the evolution of primitive bodies in the early solar system [1]. Of particular interest are the unusual trace element abundances in Stannern group eucrites, which have been interpreted as partial melting and melt contamination events that occurred on the parent body during thermal metamorphism[2]. However, some samples that contain evidence of high temperature metamorphism, such as Elephant Moraine (EET) 90020, have anomalous REE patterns that have been interpret-ed multiple ways. For example [3] concluded that the loss of small degrees of partial melt depleted the sample in LREEs while [4] concluded that subsolidus diffusion better explained why depletion of only some highly incompatible elements is observed. The heterogeneous nature of this sample makes reconstructing its petrologic history challenging. Here, we conduct further petrographic and chemical studies on polished thin sections of EET 90020 and compare results to previous studies [3-5]. Additionally, we combine chemical analyses with thermodynamic models in order to refine the constraints on the post-crystallization thermal history of EET 90020. We additionally include studies of Graves Nunataks (GRA) 98098, which also contains evidence of high temperature metamorphism and anomalous geochemical signatures, as well as evidence of solid state diffusion at lower temperatures [6].

Gorce, Jennifer S.↗

Evolution of Martian Volcanism and Lithosphere: Geochemical Insights from Noachian to Amazonian Volcanic Terrains

The lithosphere of Mars has played a crucial role in shaping its geological features, influencing volcanic activity, climate shifts, and the planet's early habitability. Understanding the evolution of Mars' litho-sphere through different geological eons has been challenging due to weathering and resurfacing affecting the study of early Noachian volcanic chemistry. Therefore, in our study we have focused on recently discovered Noachian volcanic terranes [1-2], along with Hesperian and Amazonian volcanic terranes [3], to trace the evolution of the Martian lithosphere and thermal flux. The composition of igneous rock formed from the eruption of magma tends to preserve the record of thermal properties viz. pressure, temperature, or degree of partial melting at which it forms. Therefore, Martian volcanic provinces are of great geologic interest; they have been active throughout its history, from Noachian (>3.7 Ga) to the Late Amazonian (<500 Ma) [4]. Earlier studies focused on the evolved magmatism from Hesperian to Amazonian [4], but the type and style of Noachian-aged volcanism remain to be understood. We have investigated the geochemical compositions of Noachian volcanic provinces and compared them with relatively younger volcanic provinces on Mars using remote sensing (Mars Odyssey Gamma Ray and Neutron Spectrometer suite-GRS) and in-situ observations. Furthermore, petrologic modeling is performed to understand magmatic processes and thermal evolution. Our findings reveal distinct Pressure-Temperature (P-T) conditions across different Martian geological eras. In the Noachian terranes, we model P-T conditions ranging from 1.3-1.6 GPa and temperatures between 1350-1390°C. Conversely, the Hesperian volcanic terrane exhibits variations between 1.6-1.7 GPa and temperatures spanning 1370-1395°C. For the Amazonian volcanic terrane, P-T conditions ranged notably higher, from 1.9-2.8 GPa with temperatures between 1380-1415°C. Based on our modeling, we estimated the corresponding litho-spheric thicknesses and depths of melting for each eon. In the Noachian, the lithospheric thickness ranged from 110-135 km. Meanwhile, for the Hesperian terranes, it varied between 120-235 km, and for the Amazonian, it extended from 160-235 km. We also calculated partial melting percentages (F), observing a range of 8-12% for the Noachian, 10-11% for the Hesperian, and 10-12% for the Amazonian. Mantle potential temperatures (Tp) were calculated to illustrate variations across these geological eons. Our estimates of heat flux depicted temporal changes, showing ranges from 51-65 mW/m 2 for the Noachian, 38-45 mW/m 2 for the Hesperian, and 27-39 mW/m 2 for the Amazonian. Our study implies that the lithosphere remained consistently uniform until the Hesperian eon, indicating sustained weaker volcanic systems from mid-Noachian to Hesperian. This contrasts with fewer deep-seated plumes observed in the Amazonian era. These variations suggest potential implications for Martian climatic conditions which show a milder climate prevailed until the Hesperian, differing from Mars' current cold, arid conditions.

Mars↗

Metal dynamics in Lake Vanda (Wright Valley, Antarctica)

Data are reported for Mn, Fe, Co, Ni, Cu and Cd in the Onyx River, and for Mn, Co, Ni, Cu and Cd in Lake Vanda, a closed-basin Antarctic lake. Oxic water concentrations for Co, Ni, Cu and Cd were quite low and approximate pelagic ocean values. Scavenging of these metals by sinking particles is strongly indicated. Deep-lake profiles reveal a sharp peak in the concentrations of Mn, Fe and Co at the oxic-anoxic boundary at 60 m. Maxima for Ni, Cu and Cd occur higher in the water column, in the vicinity of a Mn submaximum, suggesting early release of these metals from sinking manganese oxide-coated particles. A rough steady-state model leads to the conclusion that there is a large downward flux of Mn into the deep lake and that this flux is sufficient to explain the annual loss of Co, Ni, Cu and Cd. A pronounced geochemical separation between Fe and Mn apparently occurs in this system--Fe being best lost in near-shore environments and Mn being lost in deeper waters. Comparison of metal residence times in Lake Vanda with those in the oceans shows that in both systems Mn, Fe and Co are much more reactive than Ni, Cu and Cd. Energetically favorable inclusion of the more highly charged metals, Mn(IV), Fe(III) and Co(III), into oxide-based lattices is a plausible explanation.

NASA Center ARC↗