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At least 235 records · Page 13

Geochemistry of Pallasite Olivines and the Origin of Main-Group Pallasites

Main-group pallasites (PMG) are mixtures of iron-nickel metal and magnesian olivine thought to have been formed at the core-mantle boundary of an asteroid [1]. Some have anomalous metal compositions (PMG-am) and a few have atypically ferroan olivines (PMG-as) [2]. PMG metal is consistent with an origin as a late fractionate of the IIIAB iron core [2]. Most PMG olivines have very similar Fe/Mg ratios, likely due to subsolidus redox reaction with the metal [3]. In contrast, minor and trace elements show substantial variation, which may be explained by either: (i) PMG were formed at a range of depths in the parent asteroid; the element variations reflect variations in igneous evolution with depth, (ii) the pallasite parent asteroid was chemically heterogeneous; the heterogeneity partially survived igneous processing, or (iii) PMG represent the core-mantle boundaries of several distinct parent asteroids [4, 5]. We have continued doing major, minor and trace elements by EMPA and INAA on a wider suite of PMG olivines, and have begun doing precise oxygen isotope analyses to test these hypotheses. Manganese is homologous with Fe(2+), and can be used to distinguish between magmatic and redox processes as causes for Fe/Mg variations. PMG olivines have a range in molar 1000*Mn/Mg of 2.3-4.6 indicating substantial igneous fractionation in olivines with very similar Fe/Mg (0.138-0.148). The Mg-Mn-Fe distributions can be explained by a fractional crystallization-reduction model; higher Mn/Mg ratios reflect more evolved olivines while Fe/Mg is buffered by redox reactions with the metal. There is a positive association between Mn/Mg and Sc content that is consistent with igneous fractionation. However, most PMG olivines fall within a narrow Mn/Mg range (3.0-3.6), but these show a substantial range in Sc (1.00-2.29 micro-g/g). Assuming fractional crystallization, this Sc range could have resulted from approx.65% crystallization of an ultramafic magma. This is inconsistent with formation at the core-mantle boundary of a single asteroid [4]. One alternative is that the PMG are fragments of several asteroids, and these could have had different initial Sc contents, Mn/Mg and differences in igneous history. Our preliminary O isotope data and those of [6, 7] do not support this, although the coverage of PMG olivines is incomplete. The PMG-as Springwater is not easily fit in any scenario. Its olivine has among the highest Mn/Mg suggesting it is one of the most evolved, but the lowest Sc content suggesting it is the least evolved. The O isotopic composition of Springwater olivine is the same as that of other PMG. Thus there is no indication that it represents a distinct parent asteroid. Our preliminary O isotopic data favor a single PMG parent asteroid. In this case, the olivines are more likely melt-residues, and that the parent asteroid was initially heterogeneous in chemical, but not isotopic, composition.

Mittlefehldt, D. W.↗

Crystal Field Effects and Siderophile Element Partitioning: Implications for Mars HSE Geochemistry

Analyses of martian (SNC) meteorites indicate that Pt abundances do not vary much compared to other highly siderophile elements (HSE). Therefore, Jones et al. [1] inferred that D(Pt) during basalt petrogenesis was of order unity. This inference was at odds with previously published experiments that gave a D(sub ol/liq) for Pt of approx. 0.01 [2]. Because olivine is likely to be an important constituent of any reasonable martian mantle, the implication of these findings is that minor minerals must have D(Pt) much greater than 1, which seemed improbable. However, not only did the SNC evidence point to a D(sub ol/liq) approx. equal to 1, but so did plots of D(sub ol/liq) vs. ionic radius (Onuma diagram). The ionic radius of Pt(2+) suggested that D(sub ol/liq) for Pt was of order unity, in agreement with the inferences from SNC meteorites. New experiments have failed to detect measurable Pt in olivine, even at high oxygen fugacities [3]. Therefore, some other parameter, other than ionic charge and radius, must hold sway during olivine liquid partitioning of Pt.

Jones, John H.↗

Petrology and Geochemistry of New Ureilites and Ureilite Genesis

Ureilites are C-bearing, basalt-depleted olivine+pyroxene achondrites from a differentiated asteroid. The group is heterogeneous, exhibiting ranges in O isotopic composition, Fe/Mg, Fe/Mn, pyx/ol, siderophile and lithophile trace element content, and C content and isotopic composition [1]. Some of these characteristics are nebular in origin; others were strongly overprinted by asteroidal igneous processes. The consensus view is that most ureilites are melt-residues, but some are partial cumulates or have interacted with a melt [1,2]. An "unroofing" event occurred while the parent asteroid was hot that froze in mineral core com-positions and resulted in FeO reduction at olivine grain margins. We have studied several new ureilites, but will focus here on two anomalous stones; LAR 04315 and NWA 1241. LAR 04315 is texturally unusual. It contains olivine with angular subdomains, and low-Ca pyroxene riddled with wormy inclusions of metal+troilite, graphite, and possibly other phases, and irregular inclusions of high-Ca pyroxene. Reduction occurred along olivine grain margins and internal fractures, but not along subdomain boundaries. Although texturally odd, LAR 04351 is a typical ureilite in mineral and bulk composition. The olivine is Fo80.8 and falls on the ureilite Fe/Mn-Fe/Mg trend. Its olivine composition falls within the range of the majority of ureilites, and it is typical of these ureilites in bulk rock lithophile and siderophile element contents.

Mittlefehldt, David W.↗

Confirmation of Soluble Sulfate at the Phoenix Landing Site: Implications for Martian Geochemistry and Habitability

Over the past several decades, elemental sulfur in martian soils and rocks has been detected by a number of missions using X-ray spectroscopy [1-3]. Optical spectroscopy has also provided evidence for widespread sulfates on Mars [4,5]. The ubiquitous presence of sulfur in soils has been interpreted as a widely distributed sulfate mineralogy [6]. However, direct confirmation as to the identity and solubility of the sulfur species in martian soil has never been obtained. One goal of the Wet Chemistry Laboratory (WCL) [7] on board the 2007 Phoenix Mars Lander [8] was to determine soluble sulfate in the martian soil. The WCL received three primary samples. Each sample was added to 25 mL of leaching solution and analysed for solvated ionic species, pH, and conductivity [9,10]. The analysis also showed a discrepancy between charge balance, ionic strength, and conductivity, suggesting unidentified anionic species.

Kounaves, S. P.↗

Planetary Geochemistry Using Active Neutron and Gamma Ray Instrumentation

The Pulsed Neutron Generator-Gamma Ray And Neutron Detector (PNG-GRAND) experiment is an innovative application of the active neutron-gamma ray technology so successfully used in oil field well logging and mineral exploration on Earth, The objective of our active neutron-gamma ray technology program at NASA Goddard Space Flight Center (NASA/GSFC) is to bring the PNG-GRAND instrument to the point where it can be flown on a variety of surface lander or rover missions to the Moon, Mars, Venus, asterOIds, comets and the satellites of the outer planets, Gamma-Ray Spectrometers have been incorporated into numerous orbital planetary science missions and, especially in the case of Mars Odyssey, have contributed detailed maps of the elemental composition over the entire surface of Mars, Neutron detectors have also been placed onboard orbital missions such as the Lunar Reconnaissance Orbiter and Lunar Prospector to measure the hydrogen content of the surface of the moon, The DAN in situ experiment on the Mars Science Laboratory not only includes neutron detectors, but also has its own neutron generator, However, no one has ever combined the three into one instrument PNG-GRAND combines a pulsed neutron generator (PNG) with gamma ray and neutron detectors to produce a landed instrument that can determine subsurface elemental composition without drilling. We are testing PNG-GRAND at a unique outdoor neutron instrumentation test facility recently constructed at NASA/GSFC that consists of a 2 m x 2 m x 1 m granite structure in an empty field, We will present data from the operation of PNG-GRAND in various experimental configurations on a known sample in a geometry that is identical to that which can be achieved on a planetary surface. We will also compare the material composition results inferred from our experiments to both an independent laboratory elemental composition analysis and MCNPX computer modeling results,

Parsons, A.↗

Petrography and Geochemistry of Metals in Almahata Sitta Ureilites

Ureilites are ultramafic achondrites, predominantly composed of olivine and pyroxenes with accessory carbon, metal and sulfide. The majority of ureilites are believed to represent the mantle of the ureilite parent body (UPB) [1]. Although ureilites have lost much of their original metal [2], the metal that remains retains a record of the formative processes. Almahata Sitta is predominantly composed of unbrecciated ureilites with a wide range of silicate compositions [3,4]. As a fall it presents a rare opportunity to examine fresh ureilite metal in-situ, and analyzing their highly siderophile element (HSE) ratios gives clues to their formation. Bulk siderophile element analyses of Almahata Sitta fall within the range observed in other ureilites [5]. We have examined the metals in seven ureilitic samples of Almahata Sitta (AS) and one associated chondrite fragment (AS#25).

Ross, A. J.↗

Planetary Geochemistry Techniques: Probing In-Situ with Neutron and Gamma Rays (PING) Instrument

The Probing In situ with Neutrons and Gamma rays (PING) instrument is a promising planetary science application of the active neutron-gamma ray technology so successfully used in oil field well logging and mineral exploration on Earth. The objective of our technology development program at NASA Goddard Space Flight Center's (NASA/GSFC) Astrochemistry Laboratory is to extend the application of neutron interrogation techniques to landed in situ planetary composition measurements by using a 14 MeV Pulsed Neutron Generator (PNG) combined with neutron and gamma ray detectors, to probe the surface and subsurface of planetary bodies without the need to drill. We are thus working to bring the PING instrument to the point where it can be flown on a variety of surface lander or rover missions to the Moon, Mars, Venus, asteroids, comets and the satellites of the outer planets.

Parsons, A.↗

Laboratory Simulations of Mars Evaporite Geochemistry

Evaporite-rich sedimentary deposits on Mars were formed under chemical conditions quite different from those on Earth. Their unique chemistries record the chemical and aqueous conditions under which they were formed and possibly subsequent conditions to which they were subjected. We have produced evaporite salt mineral suites in the laboratory under two simulated Martian atmospheres: (1) present-day and (2) a model of an ancient Matian atmosphere rich in volcanic gases. The composition of these synthetic Mars evaporites depends on the atmospheres under which they were desiccated as well as the chemistries of their precursor brines. In this report, we describe a Mars analog evaporite laboratory apparatus and the experimental methods we used to produce and analyze the evaporite mineral suites.

Moore, Jeffrey M.↗

Geochemistry at 4 Vesta: Observations Using Fast Neutrons

Dawn is currently in orbit around the asteroid 4 Vesta, and one of the major objectives of the mission is to probe the relationship of Vesta to the Howardite, Eucrite, and Diogenite (HED) meteorites. As Vesta is an example of a differentiated planetary embryo, Dawn will also provide fundamental information about planetary evolution in the early solar system [1]. To help accomplish this overall goal, the Dawn spacecraft carries the Gamma-Ray and Neutron Detector (GRaND). GRaND uses planetary gamma-ray and neutron spectroscopy to measure the surface elemental composition of Vesta and will provide information that is unique and complementary to that provided by the other Dawn instruments and investigations. Gamma-ray and neutron spectroscopy is a standard technique for measuring planetary compositions [2], having successfully made measurements at near-Earth asteroids, the Moon, Mars, Mercury and now Vesta. GRaND has made the first measurements of the neutron spectrum from any asteroid (previous asteroid measurements were only made with gamma-rays). Dawn has been collecting data at Vesta since July 2011. The prime data collection period for GRaND is the Low-Altitude Mapping Orbit (LAMO), which started on 12 December 2011 and will last through spring 2012. During LAMO, the Dawn spacecraft orbits at an average altitude of ~210 km above the surface of Vesta, which allows good neutron and gamma-ray signals to be detected from Vesta. A description of the overall goals of GRaND and a summary of the initial findings are given elsewhere [3,4]. The subject of this study is to present the information that will be returned from GRaND using fast neutron measurements. Here, we discuss what fast neutrons can reveal about Vesta s surface composition, how such data can address Dawn science goals, and describe fast neutron measurements made in the early portion of the Vesta LAMO phase.

Lawrence, David J.↗

Geochemistry of Lunar Highland Meteorites Mil, 090034, 090036 AND 090070

Apollo and Luna samples were collected from a restricted area on the near side of the Moon, while the source craters of the lunar meteorites are randomly distributed. For example, Takeda et al. [1] and Yamaguchi et al. [2] found a variety of lithic clasts in Dho 489 and Y 86032 which were not represented by Apollo samples, and some of these clasts have lower rare earth elements (REE) and FeO abundances than Apollo anorthosites, respectively. Takeda et al. [1] and Yamaguchi et al. [2] concluded that Dho 489 and Y 86032 originated from the lunar farside. Therefore, lunar meteorites provide an opportunity to study lunar surface rocks from areas not sampled by Apollo and Luna missions. Three lunar anorthitic breccias (MIL 090034, 090036 and 090070) were found on the Miller Range Ice Field in Antarctica during the 2009-2010 ANSMET season [3]. In this study, we determined elemental abudnances for MIL 090034, 090036 and 090070 by using INAA and aimed to characterize these meteorites in chemical compositions in comparison with those for other lunar meteorites and Apollo samples.

Shirai, N.aoki↗

Organic Geochemistry of the Hamersley Province: Relationships Among Organic Carbon Isotopes, Molecular Fossils, and Lithology

Molecular fossils are particularly valuable ancient biosignatures that can provide key insight about microbial sources and ecology in early Earth studies. In particular, hopanes carrying 2-methyl or 3-methyl substituents are proposed to be derived from cyanobacteria and oxygen-respiring methanotrophs, respectively, based on both their modem occurrences and their Proterozoic and Phanerozoic sedimentary distributions. Steranes are likely from ancestral eukaryotes. The distribution of methylhopanes, steranes, and other biomarkers in 2.72-2.56 billion-year-old rocks from the Hamersley Province, Western Australia show relationships to lithology, facies, and isotopes of macromolecular carbon, and other biomarkers. These observations support biomarker syngenicity and thermal maturity. Moreover, ecological signatures are revealed, including a surprising relationship between isotopic values for bulk macromolecular carbon and the biomarker for methanotrophs. The record suggests that cyanobacteria were likely key organisms of shallow-water microbial ecosystems providing molecular oxygen, fixed carbon, and possibly fixed nitrogen, and methanotrophs were not alone in recycling methane and other C-13-depleted substrates.

Eigenbrode, Jennifer L.↗

Martian Igneous Geochemistry: The Nature of the Martian Mantle

Mafic igneous rocks probe the interiors of their parent objects, reflecting the compositions and mineralogies of their source regions, and the magmatic processes that engendered them. Incompatible trace element contents of mafic igneous rocks are widely used to constrain the petrologic evolution of planets. We focus on incompatible element ratios of martian meteorites to constrain the petrologic evolution of Mars in the context of magma ocean/cumulate overturn models [1]. Most martian meteorites contain some cumulus grains, but regardless, their incompatible element ratios are close to those of their parent magmas. Martian meteorites form two main petrologic/ age groupings; a 1.3 Ga group composed of clinopyroxenites (nakhlites) and dunites (chassignites), and a <1 Ga group composed of basalts and lherzolites (shergottites).

Mittlefehldt, D. W.↗

The Petrology and Geochemistry of Feldspathic Granulitic Breccia NWA 3163: Implications for the Lunar Crust

Lunar meteorites are crucial to understand the Moon s geological history because, being samples of the lunar crust that have been ejected by random impact events, they potentially originate from areas outside the small regions of the lunar surface sampled by the Apollo and Luna missions. The Apollo and Luna sample sites are contained within the Procellarum KREEP Terrain (PKT, Jolliff et al., 2000), where KREEP refers to potassium, rare earth element, and phosphorus-rich lithologies. The KREEP-rich rocks in the PKT are thought to be derived from late-stage residual liquids after approx.95-99% crystallization of a lunar magma ocean (LMO). These are understood to represent late-stage liquids which were enriched in incompatible trace elements (ITE) relative to older rocks (Snyder et al., 1992). As a consequence, the PKT is a significant reservoir for Th and KREEP. However, the majority of the lunar surface is likely to be significantly more depleted in ITE (84%, Jolliff et al., 2000). Lunar meteorites that are low in KREEP and Th may thus sample regions distinct from the PKT and are therefore a valuable source of information regarding the composition of KREEP-poor lunar crust. Northwest Africa (NWA) 3163 is a thermally metamorphosed ferroan, feldspathic, granulitic breccia composed of igneous clasts with a bulk anorthositic, noritic bulk composition. It is relatively mafic (approx.5.8 wt.% FeO; approx.5 wt.% MgO) and has some of the lowest concentrations of ITEs (17ppm Ba) compared to the feldspathic lunar meteorite (FLM) and Apollo sample suites (Hudgins et al., 2011). Localized plagioclase melting and incipient melting of mafic minerals require localized peak shock pressures in excess of 45 GPa (Chen and El Goresy, 2000; Hiesinger and Head, 2006). NWA 3163, and paired samples NWA 4481 and 4883, have previously been interpreted to represent an annealed micro-breccia which was produced by burial metamorphism at depth in the ancient lunar crust (Fernandes et al., 2009). This is in contrast to the interpretation of Hudgins et al. (2009) where NWA 3163 was interpreted to have formed through contact metamorphism. To further constrain its origin, we examine the petrogenesis of NWA 3163 with a particular emphasis on in-situ measurement of trace elements within constituent minerals, Sm-Nd and Rb-Sr isotopic systematics on separated mineral fractions and petrogenetic modeling.

McLeod, C. L.↗

Petrography and Geochemistry of Feldspathic Lunar Meteorite Larkman Nunatak 06638

LAR 06638 is a glassy-matrix lunar regolith breccia based on the presence of glass spherules, which also contains prominent clasts of a feldspathic fragmental breccia lithology. The similarity in composition of the two lithologies is unsurprising given the observed similarities in the clast populations and mineral compositions in both lithologies. The small differences in composition are likely explained by the incorporation of small amounts of more diverse material into the regolith breccia lithologies, e.g., KREEPy glass clasts to account for the higher siderophile and ITE concentrations and excess plagioclase to account for the lower concentrations of mafic elements and increased Na concentrations. Given the relatively small masses analyzed (approx.120 mg of each lithology), these small compositional differences could also be sampling effects. The presense of multiple generations of glass coatings on LAR 06638 is, to our knowledge, unique among lunar meteorites. The more mafic, schlieren and nanophase Fe bearing glass is similar in morphology to the South Ray Crater glass coatings at the Apollo 16 site [3] and likely has a similar origin. The outer, more feldspathic glass has a morphology typical of fusion crust observed on other feldspathic lunar meteorites. It is unclear at this time whether the partially melted glass area represents a partially formed fusion crust or incipient melting due to heating on the lunar surface, likely from an overlying (and possibly ablated) glass splash coating. LAR 06638 is unlikely to be source-crater paired with any other lunar meteorites. For all elements, it plots right in the range of "typical feldspathic lunar meteorites" [4]. Among lunar meteorites from Antarctica, LAR 06638 most closely resembles MAC 88104/5 in composition, although it is slightly more feldspathic and 1.8 richer in siderophile elements. Compositionally it is more similar to hot-desert meteorites like Dhofar 490/1084 and NWA 2200 [4].

Zeigler, Ryan A.↗

Time-resolved Neutron-gamma-ray Data Acquisition for in Situ Subsurface Planetary Geochemistry

The current gamma-ray/neutron instrumentation development effort at NASA Goddard Space Flight Center aims to extend the use of active pulsed neutron interrogation techniques to probe the subsurface elemental composition of planetary bodies in situ. Previous NASA planetary science missions, that used neutron and/or gamma-ray spectroscopy instruments, have relied on neutrons produced from galactic cosmic rays. One of the distinguishing features of this effort is the inclusion of a high intensity 14.1 MeV pulsed neutron generator synchronized with a custom data acquisition system to time each event relative to the pulse. With usually only one opportunity to collect data, it is difficult to set a priori time-gating windows to obtain the best possible results. Acquiring time-tagged, event-by-event data from nuclear induced reactions provides raw data sets containing channel/energy, and event time for each gamma ray or neutron detected. The resulting data set can be plotted as a function of time or energy using optimized analysis windows after the data are acquired. Time windows can now be chosen to produce energy spectra that yield the most statistically significant and accurate elemental composition results that can be derived from the complete data set. The advantages of post-processing gamma-ray time-tagged event-by-event data in experimental tests using our prototype instrument will be demonstrated.

Pulsed neutrongenerator↗

Petrology and Geochemistry of Unbrecciated Harzburgitic Diogenite MIL 07001: A Window Into Vestan Geological Evolution

There is a strong case that asteroid 4 Vesta is the parent of the howardite, eucrite and diogenite (HED) meteorites. Models developed for the geological evolution of Vesta can satisfy the compositions of basaltic eucrites that dominate in the upper crust. The bulk compositional characteristics of diogenites - cumulate harzburgites and orthopyroxenites from the lower crust - do not fit into global magma ocean models that can describe the compositions of basaltic and cumulate eucrites. Recent more detailed formation models do make provision for a more complicated origin for diogenites, but this model has yet to be completely vetted. Compositional studies of bulk samples has led to the hypothesis that many diogenites were formed late by interaction of their parent melts with a eucritic crust, but those observations may alternatively be explained by subsolidus equilibration of trace elements between orthopyroxene and plagioclase and Ca-phosphate in the rocks. Differences in radiogenic Mg-26 content between diogenites and eucrites favors early formation of the former, not later formation. Understanding the origin of diogenites is crucial for understanding the petrologic evolution of Vesta. We have been doing coordinated studies of a suite of diogenites including petrologic investigations, bulk rock major and trace element studies, and in situ trace element analyses of orthopyroxene. Here we will focus on an especially unusual, and potentially key, diogenite, MIL 07001.

Mittlefehldt, D. W.↗

Peology and Geochemistry of New Paired Martian Meteorites 12095 and LAR 12240

The meteorites LAR 12095 and LAR 12240 are believed to be paired Martian meteorites and were discovered during the Antarctic Search for Meteorites (ANSMET) 2012-2013 Season at Larkman Nunatak. The purpose of this study is to characterize these olivine-phyric shergottites by analyzing all mineral phases for major, minor and trace elements and examining their textural relationships. The goal is to constrain their crystallization history and place these shergottites among other Martian meteorites in order to better understand Martian geological history.

Funk, R. C.↗

Exploring the Cloud Icy Early Mars Hypothesis Through Geochemistry and Mineralogy

While ancient fluvial channels have long been considered strong evidence for early surface water on Mars, many aspects of the fluvial morphology and occurrence suggest that they formed in relatively water limited conditions (com-pared to Earth) and that climatic excursions allowing for surface water might have been short-lived. Updated results mapping valley networks at higher resolution have changed this paradigm, showing that channels are much more abundant and wide-spread, and of higher order than was previously recognized, suggesting that Mars had a dense enough atmosphere and warm enough climate to allow channel formation up to 3.6-3.8 Ga. This revised view of the ancient martian climate might be broadly consistent with a climate history of Mars devised from infrared remote sensing of surface minerals, suggesting that widespread clay minerals formed in the Noachian, giving way to a sulfur-dominated surface weathering system by approx. 3.7 Ga.

Niles, P. B.↗