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At least 451 records · Page 25

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NASA NTRS1982

Petrogenesis of light and dark portions of the Leighton gas-rich chondritic breccia

Individual dark fractions of the Leighton chondritic breccia are all enriched in volatile/mobile trace elements. Concentrations of the most highly volatile/mobile elements correlate with degree of equilibration, as expressed by compositional variability for silicates. Individual light clasts in the same meteorite are equilibrated and generally volatile-poor, except for enrichments in Rb and Cs. These alkali elements may have been redistributed by feldspar formation during metamorphism. Enrichments of other trace elements in dark portions may have been caused by mobilization during metamorphism in the parent body interior and deposition in the cooler surface layers. An alternative model involves accretional mixing of a diverse compositional population of primitive H group materials to form dark materials. Subsequent integration of light and dark materials was accomplished by impacts into a regolith.

Mcsween, H. Y., Jr.↗

NASA NTRS1993

On the composition of neuKREEP: QMD contamination at Apollo 11?

The Group A basalts of Apollo 11 differ in many respects from other high-Ti basalts of the region. Chemically, they are the only high-K (greater than 2000 ppm K) variety of high-Ti basalt and are enriched in incompatible trace elements relative to other basalts from both the Apollo 11 and Apollo 17 sites. In addition, Group A basalts are the youngest of all high-Ti basalts, with an age of 3.56 +/- 0.02 Ga. The cluster of compositions is consistent with the Apollo 11 Group A basalts representing a single flow. Papanastassiou et al. have also indicated the uniqueness of these basalts, based particularly on relatively young Rb-Sr model ages (3.8 - 3.9 Ga). A model for the formation of the Group A basalts was presented by Jerde et al., wherein the Apollo 17 orange volcanic glass is the parent liquid. Fractionation of this composition, coupled with the assimilation of incompatible-element-rich material, results in compositions akin to those of the Apollo 11 Group A basalt population. Orange glass of similar major-element composition is present at the Apollo 11 site as well, although complete trace element analyses are not available. New modelling results using the Apollo 11 orange glass major elements are grossly similar to those obtained using the Apollo 17 orange glass, indicating approximately 30 percent fractionation.

Jerde, Eric A.↗

DOE OSTI2020

Environmental Impacts of Reclaimed Asphalt Pavement on Leaching of Metals into Groundwater

To investigate the environmental impacts of reclaimed asphalt pavement (RAP) while it was freshly processed (i.e. hot mixed asphalt or HMA) and after being subjected to weathering, three RAP materials, namely north-RAP, central-RAP, south-RAP, from three plants and one fresh HMA loose mix sample (Fresh-HMA) throughout New Jersey, USA underwent four different weathering processes including: Ultraviolet (UV) and precipitation weathering on unbounded RAP, UV and precipitation weathering on compacted RAP, weathering by heat and moisture cycles, and groundwater flow-through leaching. Batch experiments were conducted to mimic releasing of trace elements in weak acidic leachate from landfills. North-RAP and central-RAP released levels of Pb greater than the United States Environmental Protection Agency (USEPA) primary drinking water maximum contaminant level (MCL) of 15 µg/L. Novel two-column experiments (a RAP column followed by a soil column) were conducted to investigate the release of trace elements from RAP and the attenuation effect of soil on potential pollutants. The results of these experiments showed that pollutants released from RAPs such as Mn and Ni were largely attenuated in the soil. The results suggest that RAP can be used as an unbound material in environments except those acidic (i.e., pH < 5 as in mines with sulfur-containing minerals and landfills with acidic environment).

batch extraction↗

NASA NTRSDate not supplied

In-Situ XRD/XRF to Support Life Detection on Mars

X-ray diffraction / X-ray fluorescence (XRD/XRF) analysis provides the most comprehensive mineralogical / compositional characterization of rocks and soils of any flight-capable technique. XRD data provide quantitative mineralogy (including abundance of X-ray amorphous materials) and crystal chemistry (structure, elemental composition and valence state), and XRF data provide complimentary major, minor, and some trace element abundances. Both types of data are important in evaluating habitability (environment of formation) and biosignature preservation/degradation (post-depositional diagenetic change). Whether or not a relict biosignature is detected, the mineral assemblage and its geochemistry can be used to determine the habitability of an ancient environment (e.g., salinity, pH, temperature), and to identify potential sources of energy for life (e.g., elements in different redox states). In this respect, a null result (a habitable environment lacking evidence of life) can play an important role in constraining the parameters of the search. Conversely, diagenetic alteration (taphonomic change) resulting from post-depositional variations in temperature, pressure or fluid chemistry can preserve evidence of biogenicity, erase such evidence completely or indeed can provide for post-depositional habitable conditions in the subsurface. XRD / XRF data are critical to these determinations. The CheMin instrument on the Mars Science Laboratory (MSL) Curiosity rover is the first XRD instrument flown in space. CheMin operates in transmission geometry with a Co X-ray source to minimize fluorescence from iron. Diffracted photons are collected with an energy-sensitive charge-coupled device (CCD). The position of the diffracted photons provides structural information for minerals, whereas the energy of sample-generated X-ray fluorescence photons provides elemental information, though these XRF data are qualitative. Mineralogical data from the CheMin XRD identified the three circumstances above: habitable depositional environments (e.g., Yellowknife Bay), habitable subsurface/diagenetic environments (e.g., throughout the Murray formation), and diagenetic conditions that may destroy evidence of habitability (e.g., oxidative and acidic environments at Vera Rubin ridge). Technological advances in X-ray technology and lessons learned from the operation of CheMin on Mars have resulted in a next-generation XRD/XRF, called CheMinX. Replacement of CheMin’s CCD with an array of hybrid pixel detectors and improvements in focusing optics dramatically decrease analysis time (15 minutes vs. 22 hours for MSL-CheMin) and result in a better angular resolution (0.18 vs. 0.30 °2θ for MSL-CheMin). This increased resolution improves mineral detection, including discrimination between types of pyroxenes, which is not possible with MSL-CheMin data. The hybrid pixel detectors do not require cooling like the MSL-CheMin CCD, therefore reducing the power needed to operate CheMinX. CheMinX has a silicon-drift detector (SDD) to measure fluoresced photons, enabling the quantification of major, minor, and some trace elements via XRF. XRD/XRF data are collected simultaneously in CheMinX, obviating the need for multiple compositional instruments. The CheMinX design also improves upon MSL-CheMin’s sample handling. Instead of sample cells on wheel, which are often not reusable and add complexity in commanding the instrument, CheMinX has single-use cells in a cartridge/dispenser configuration. Because of these improvements, CheMinX is an ideal instrument for Discovery-class life-detection missions, including Mars Life Explorer that was recommended for development in the Planetary Science and Astrobiology Decadal Survey 2023-2032.

E B Rampe↗

NASA NTRS1983

Use of olivine and plagioclase saturation surfaces for the petrogenetic modeling of recrystallized basic plutonic systems

During petrogenetic studies of basic plutonic rocks, there are at least three major questions to be considered: (1) what were the relative proportions of cumulate crystals and intercumulus melt in a given sample? (2) what is the composition and variation in composition of the melts within the pluton? and (3) what is the original composition of the liquids, their source and evolution prior to the time of emplacement? Use of both saturation surfaces can place strong limits on the compositions of potential cumulate phases and intercumulus melts. Consideration of appropriate trace elements can indicate whether a sample is an orthocumulate, adcumulate or mesocumulate. Thus, when trace element and petrographic data are considered together with the saturation surfaces, it should be possible to begin to answer the three major questions given above, even for strongly recrystallized basic plutons.

Hanson, G. N.↗

NASA NTRS2002

The Meteoritic Component in Impact Deposits

An important part of the history of impacts on Earth, and their influence on the terrestrial environment and biotic evolution, is the provenance of the impacting bolides. This will reflect the history of the large-body object flux in the inner solar system. The physical and chemical properties of projectiles, as well as their orbital evolution, has influenced the dynamics and the relative timing of impact events. Possible impact scenarios include random impacts by individual asteroids or comets, or clusters of impacts due to major collisions in the asteroid or Kuiper belts, or large perturbations of the Oort cloud of comets. Over the last several years, a combination of trace element, isotopic, and petrologic data have yielded significant insights into this impact history. The trace element chemistry of sediments, in particular the concentration of siderophiles (e.g., Ir), is a useful tool to detect impacts and provides supporting evidence for suspected impact deposits. However, siderophiles are not especially useful in distinguishing between types of projectiles. Interelement abundances of PGEs can distinguish a chondritic signature, but since most asteroids, and probably all comets are chondritic, these data do little to distinguish between chondritic source materials. Perhaps the most significant chemical argument used to constrain provenance, is that the total amount of Ir in the global Cretaceous-Tertiary (KT) boundary ejecta layer is considerably less than that expected by a low-velocity, 10 km asteroid impact and is most consistent with the impact of a high-velocity, low-Ir comet. Alternatively, much of the Ir may have been buried in the Chicxulub crater and/or ejected to escape velocity.

Kyte, Frank T.↗

NASA NTRS2021

Assessing Domains of Equilibration In Highly Metamorhposed Eucrites

This study assesses how petrographic textures and trace element distributions, combined with thermodynamic models, can act as indicators of metamorphic equilibrium and/or trace element mobility in highly metamorphosed eucrite, Elephant Moraine (EET) 90020.

Thermodynamic modelling↗

NASA NTRS1973

Rb-Sr systematics for chemically defined Apollo 15 and 16 materials

Concentrations of Rb and Sr and the Sr87/86 ratios are determined in a large number of Apollo 15 samples, including KREEP basalts, mare basalts, anorthosite breccia clasts, lithic fragments, a spinel-bearing clast, green glass samples, breccia matrix, and soils. Relative concentrations of Sm, Eu, Rb, and Sr are also examined in the samples, with particular attention to Rb/Sr systematics vs other trace element abundances and total chemical compositions of rocks. Analysis of crystalline KREEP samples rich in trace elements indicates that the differentiation of these rocks has extended to -4.25 AE age, a significantly later time than the presumed time of accretion of the moon.

Nyquist, L. E.↗

NASA NTRS2021

The effects of terrestrial weathering on samarium-neodymium isotopic composition of ordinary chondrites

Following their fall to Earth, meteorites experience weathering. In this systematic study, we evaluate the trace element composition of ordinary chondrites from the Antarctic cold desert, and Atacama (Chile) and Lut (Iran) hot deserts, with an emphasis on rare earth elements (REE). Our data confirms that terrestrial weathering of meteorites in hot deserts changes their trace element (Sr, Ba, REE, Hf, Th, and U) concentrations. However, weathering effects in majority of Antarctic samples are limited to slight Ba, REE, Hf, and Th depletions and in some case to U enrichment. In comparison to the Antarctic meteorites, hot desert samples show greater disturbances and REE fractionation relative to the average fall values. We measured the Sm-Nd isotopic composition of the hot desert meteorites that have heavily affected REE compositions. Our Sm-Nd isotopic data show a significant effect of terrestrial weathering evidenced by non-CHUR (147)Sm/(144)Nd and (143)Nd/(144)Nd ratios. Measurements show a higher variation and lower values of (147)Sm/(144)Nd for the Atacama samples than those from the Lut Desert. Deviations from CHUR (147)Sm/(144)Nd value are in positive accordance with the degree of La/Lu fractionation caused by weathering. The ɛNd values of Atacama and Lut deserts meteorites range from −2.20 to +1.61, which is wider than the −1.07 to +0.64 range for falls. We suggest that disturbance of primary Sm/Nd ratios resulting from mixing with terrestrial components originating from soil during weathering is responsible for lower (147)Sm/(144)Nd ratio in these meteorites. The majority of the Atacama meteorites regardless of their weathering degrees have their REE compositions and ɛNd affected by terrestrial contamination. Both (147)Sm/(144)Nd ratio and ɛNd values show no straightforward relationship with weathering degree. However, in both cases the samples with the highest negative isotopic disturbances are H chondrites from the Atacama and Lut deserts. In addition, Ba concentration shows a negative correlation with (147)Sm/(144)Nd ratio. Care must be taken into account while dealing with samples collected from hot deserts, even fresh-looking ones.

Isotope geochemistry↗

DOE OSTI2021

Fossil Corals With Various Degrees of Preservation Can Retain Information About Biomineralization-Related Organic Material

Scleractinian corals typically form a robust calcium carbonate skeleton beneath their living tissue. This skeleton, through its trace element composition and isotope ratios, may record environmental conditions of water surrounding the coral animal. While bulk unrecrystallized aragonite coral skeletons can be used to reconstruct past ocean conditions, corals that have undergone significant diagenesis have altered geochemical signatures and are typically assumed to retain insufficient meaningful information for bulk or macrostructural analysis. However, partially recrystallized skeletons may retain organic molecular components of the skeletal organic matrix (SOM), which is secreted by the animal and directs aspects of the biomineralization process. Some SOM proteins can be retained in fossil corals and can potentially provide past oceanographic, ecological, and indirect genetic information. Here, we describe a dataset of scleractinian coral skeletons, aged from modern to Cretaceous plus a Carboniferous rugosan, characterized for their crystallography, trace element composition, and amino acid compositions. We show that some specimens that are partially recrystallized to calcite yield potentially useful biochemical information whereas complete recrystalization or silicification leads to significant alteration or loss of the SOM fraction. Our analysis is informative to biochemical-paleoceanographers as it suggests that previously discounted partially recrystallized coral skeletons may indeed still be useful at the microstructural level.

58 GEOSCIENCES↗

NASA NTRS2005

Siderophile Element Profile Measurements in Iron Meteorites Using Laser Ablation ICP-MS

Understanding the behaviour of siderophile elements during cooling of iron meteorites can lead to insight into the general thermal histories of the meteorites as well as their respective parent bodies. Traditionally trace element analyses in meteorites have been done using techniques that only measure the average concentration in each phase. With these methods, all of the spatial information with respect to the distribution of an element within one phase is lost. Measuring concentration profiles of trace elements in meteorites is now possible, with the advent of high-resolution analytical techniques such as laser ablation, inductively coupled plasma mass spectrometry (LA-ICP-MS) with spatial resolution <20 microns. [e.g. 1,2] and secondary ion mass spectrometry [3]. These profiles can give more insight into both the partitioning and diffusive behavior of siderophile elements in metal systems relevant to iron meteorites, as well as parent body cooling rates.

Watson, H. C.↗

NASA NTRS1993

Rare earth element selenochemistry of immiscible liquids and zircon at Apollo 14 - An ion probe study of evolved rocks on the moon

Results are presented of trace-element analyses of three lunar zircons. The major-element and REE compositions were determined using electron microprobes, and a correction was made for zircon for Zr-Si-O molecular interferences in the La to Pr mass region. The three zircons were found to exhibit similar REE abundances and patterns. Results of the analyses confirm earlier studies (Hess et al., 1975; Watson, 1976; Neal and Taylor, 1989) on the partitioning behavior of trace elements in immiscible liquid-liquid pairs. The results also support the postulated importance of silicate liquid immiscibility in the differentiation of the upper mantle and crust of the moon.

Snyder, Gregory A.↗

NASA NTRS1988

Volcanic ash layers in blue ice fields (Beardmore Glacier Area, Antarctica): Iridium enrichments

Dust bands on blue ice fields in Antarctica have been studied and have been identified to originate from two main sources: bedrock debris scraped up from the ground by the glacial movement (these bands are found predominantly at fractures and shear zones in the ice near moraines), and volcanic debris deposited on and incorporated in the ice by large-scale eruptions of Antarctic (or sub-Antractic) volcanoes. Ice core studies have revealed that most of the dust layers in the ice cores are volcanic (tephra) deposits which may be related to some specific volcanic eruptions. These eruptions have to be related to some specific volcanic eruptions. These eruptions have to be relatively recent (a few thousand years old) since ice cores usually incorporate younger ice. In contrast, dust bands on bare blue ice fields are much older, up to a few hundred thousand years, which may be inferred from the rather high terrestrial age of meteorites found on the ice and from dating the ice using the uranium series method. Also for the volcanic ash layers found on blue ice fields correlations between some specific volcanoes (late Cenozoic) and the volcanic debris have been inferred, mainly using chemical arguments. During a recent field expedition samples of several dust bands found on blue ice fields at the Lewis Cliff Ice Tongue were taken. These dust band samples were divided for age determination using the uranium series method, and chemical investigations to determine the source and origin of the dust bands. The investigations have shown that most of the dust bands found at the Ice Tongue are of volcanic origin and, for chemical and petrological reasons, may be correlated with Cenozoic volcanoes in the Melbourne volcanic province, Northern Victoria Land, which is at least 1500 km away. Major and trace element data have been obtained and have been used for identification and correlation purposes. Recently, some additional trace elements were determined in some of the dust band samples, including Ir. Iridium determinations were made using INAA, with synthetical and natural (meteorite) standards. These findings are discussed.

Koeberl, Christian↗

NASA NTRS1990

Petrogenesis of mesosiderites. I - Origin of mafic lithologies and comparison with basaltic achondrites

New petrologic and trace element data on basaltic and gabbroic clasts in mesosiderites and basaltic achondrites, combined with existing petrologic and trace element data, have served as a basis for interpretation of the petrogenesis of mesosiderite clasts. Compared with the basaltic achondrites, the mesosiderite basaltic and gabbroic clasts contain more abundant modal tridymite and merrilite, and more commonly contain augite as a late magmatic phase. Their pyroxenes tend to be more MgO-rich, and have lower Fe/Mn ratios which are positively correlated with the Fe/Mg ratio. Some of the mesosiderite basaltic and gabbroic clasts contain xenocrystic plagioclase. The basaltic clasts commonly show superchondritic Eu/Sm ratios and slight LREE depletions. The cumulate gabbro clasts are extremely depleted in LIL, have very high Eu/Sm ratios and high Lu/Sm ratios. All of these features can be explained by a model in which the mafic lithologies of mesosiderites were formed by remelting of a mixed basalt-cumulate gabbro-metal source region near the parent body surface.

Mittlefehldt, David W.↗

NASA NTRS1978

Silicate spherules from deep-sea sediments - Confirmation of extraterrestrial origin

Silicate spherules larger than 100 microns were extracted from 100 kg of box core samples of Pacific red clay taken in the mid-Pacific at a depth of 5 km, and the concentration of nonvolatile trace elements was determined for three spheres. One of the spheres shows excellent resemblance to C1 chondrite nonvolatile trace-element abundance patterns, and the relative abundances of the other two spheres are also very similar to those of C1 chondrites. One of these two spheres is depleted in Ir and Ru, while the other is depleted for Ni and Cr; possible explanations for the depletions are considered. Since the elemental abundances of the third sphere match the abundances of C1 chondrites, it is suggested that this sphere must be of extraterrestrial origin.

Ganapathy, R.↗

NASA NTRS1993

Orthopyroxenes as recorders of diogenite petrogenesis: Major and minor element systematics

As a part of our research to better understand magmatic processes in the Eucrite Parent Body, we have initiated an ambitious program of study of major, minor and trace elements in orthopyroxene from diogenites. This paper reports preliminary results for major and minor elements in orthopyroxenes for a suite of 13 diogenites: Aioun El Atrouss, ALH 84001, ALH A 77256, EET 87530, Ellemeet, Garland, Ibbenburen, Johnstown, Manegoan, peckelsheim, Roda, Shalka, and Tatahouine. A companion paper by Shearer et al. reports new trace element data for ALH 84001, ALH A 77256, Ibbenburen, and Tatahouine. We have presently collected over 800 high quality pyroxene microprobe analyses for Si, Al, Ca, Na, Mn, Fe, Mg, Cr, and Ti. The chemical systematics observed for these orthopyroxenes reflect original magmatic mineral/melt partitioning plus later trapped liquid/mineral equilibration, subsolids, exsolution, and mineral/mineral metamorphic reactions. We have therefore avoided, at this point, any attempt to use statistical analysis to group (e.g. factor or cluster analysis) these orthopyroxenes chemically.

Papike, J. J.↗

NASA NTRS1984

Chemical substitution in silica polymorph

Ion and electron probe analyses are presented for trace elements (Al, Na, K, Li, Ti) in quartz, tridymite, cristobalite and melanophlogite. Quartz and melanophlogite show low levels of trace elements relative to tridymite and cristobalite. The previously determined alpha-beta inversion temperature decreases as the Al content of quartz increases. For all silica polymorphs, Al is greater than or equal to Na + K + Li on an atom basis, with the excess Al probably balanced by H.

Smith, J. V.↗

NASA NTRS1990

Synchrotron X-ray fluorescence analyses of stratospheric cosmic dust - New results for chondritic and low-nickel particles

Trace element abundance determinations were performed using synchrotron X-ray fluorescence on nine particles collected from the stratosphere and classified as cosmic. Improvements to the Synchrotron Light Source allowed the detection of all elements between Cr and Mo, with the exceptions of Co and As, in our largest particle. The minor and trace element abundance patterns of three Ni-depleted particles were remarkably similar to those of extraterrestrial igneous rocks. Fe/Ni and Fe/Mn ratios suggest that one of these may be of lunar origin. All nine particles exhibited an enrichment in Br, ranging from 1.3 to 38 times the C1 concentration. Br concentrations were uncorrelated with particle size, as would be expected for a surface correlated component acquires from the stratosphere.

Flynn, G. J.↗