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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS1998

Comparison of Martian Meteorites and Martian Regolith as Shield Materials for Galactic Cosmic Rays

Theoretical calculations of radiation attenuation due to energetic galactic cosmic rays behind Martian rock and Martian regolith material have been made to compare their utilization as shields for advanced manned missions to Mars because the detailed chemical signature of Mars is distinctly different from Earth. The modified radiation fields behind the Martian rocks and the soil model were generated by solving the Boltzmann equation using a HZETRN system with the 1977 Solar Minimum environmental model. For the comparison of the attenuation characteristics, dose and dose equivalent are calculated for the five different subgroups of Martian rocks and the Martian regolith. The results indicate that changes in composition of subgroups of Martian rocks have negligible effects on the overall shielding properties because of the similarity of their constituents. The differences for dose and dose equivalent of these materials relative to those of Martian regolith are within 0.5 and 1 percent, respectively. Therefore, the analysis of Martian habitat construction options using in situ materials according to the Martian regolith model composition is reasonably accurate. Adding an epoxy to Martian regolith, which changes the major constituents of the material, enhances shielding properties because of the added hydrogenous constituents.

Kim, Myung-Hee Y.↗
NASA NTRS1988

Absolute ages from crater statistics: Using radiometric ages of Martian samples for determining the Martian cratering chronology

In the absence of dates derived from rock samples, impact crater frequencies are commonly used to date Martian surface units. All models for absolute dating rely on the lunar cratering chronology and on the validity of its extrapolation to Martian conditions. Starting from somewhat different lunar chronologies, rather different Martian cratering chronologies are found in the literature. Currently favored models are compared. The differences at old ages are significant, the differences at younger ages are considerable and give absolute ages for the same crater frequencies as different as a factor of 3. The total uncertainty could be much higher, though, since the ratio of lunar to Martian cratering rate which is of basic importance in the models is believed to be known no better than within a factor of 2. Thus, it is of crucial importance for understanding the the evolution of Mars and determining the sequence of events to establish an unambiguous Martian cratering chronology from crater statistics in combination with clean radiometric ages of returned Martian samples. For the dating goal, rocks should be as pristine as possible from a geologically simple area with a one-stage emplacement history of the local formation. A minimum of at least one highland site for old ages, two intermediate-aged sites, and one very young site is needed.

Neukum, G.↗
NASA NTRS1992

Chemical modeling constraints on Martian surface mineralogies formed in an early, warm, wet climate, and speculations on the occurrence of phosphate minerals in the Martian regolith

This is one in a series of reports summarizing our chemical modeling studies of water-rock-gas interactions at the martian surface through time. The purpose of these studies is to place constraints on possible mineralogies formed at the martian surface and to model the geochemical implications of martian surficial processes proposed by previous researchers. Plumlee and Ridley summarize geochemical processes that may have occurred as a result of inferred volcano- and impact-driven hydrothermal activity on Mars. DeBraal et al. model the geochemical aspects of water-rock interactions and water evaporation near 0 C, as a prelude to future calculations that will model sub-0 C brine-rock-clathrate interactions under the current martian climate. In this report, we discuss reaction path calculations that model chemical processes that may have occurred at the martian surface in a postulated early, warm, wet climate. We assume a temperature of 25 C in all our calculations. Processes we model here include (1) the reaction of rainwater under various ambient CO2 and O2 pressures with basaltic rocks at the martian surface, (2) the formation of acid rain by volcanic gases such as HCl and SO2, (3) the reactions of acid rain with basaltic surficial materials, and (4) evaporation of waters resulting from rainwater-basalt interactions.

Plumlee, Geoffrey S.↗
NASA NTRS1999

Radiometric Ages of Martian Meteorites compared to Martian Surfaces Ages

The surprisingly young Rb-Sr age of the Shergotty meteorite contributed to early suggestions that it might be of martian origin. their redox state and oxygen isotopic compositions linked the shergottites to the clino-pyroxenite nakhlites and the dunite Chassigny, causing them to be grouped as SNC meteorites. These characteristics, but especially the similarity of the elemental and isotopic compositions of gases trapped in shergottites to those of the martian atmosphere, have caused the martian origin of the SNC and related meteorites to be widely accepted. Although the young ages were one of the early hints of a martian origin for the SNC meteorites, their interpretation has remained somewhat ambiguous. We will review the radiometric ages of the martian meteorites and attempt to place them into the context of martian surface ages.

Nyquist, L. E.↗
NASA NTRS2004

Composition of Simulated Martian Brines and Implications for the Origin of Martian Salts

We report on laboratory experiments that have produced dilute brines under controlled conditions meant to simulate past and present Mars. We allowed an SNC-derived mineral mix to react with pure water under a simulated present-Mars atmosphere for seven months. We then subjected the same mineral mix to a similar aqueous environment for one year, but with a simulated Mars atmosphere that contained the added gases SO2, HCl and NO2. The addition of acidic gases was designed to mimic the effects of volcanic gases that may have been present in the martian atmosphere during periods of increased volcanic activity. The experiments were performed at one bar and at two different temperatures in order to simulate subsurface conditions where liquid water and rock are likely to interact on Mars. The dominant cations dissolved in the solutions we produced were Ca(2+), Mg(2+), Al(3+) and Na(+), while the major anions are dissolved C, F(-), SO4(2-) and Cl(-). Typical solution pH was 4.2 to 6.0 for experiments run with a Mars analog atmosphere, and 3.6-5.0 for experiments with acidic gases added. Abundance patterns of elements in the synthetic sulfate-chloride brines produced under acidic conditions were distinctly unlike those of terrestrial ocean water, terrestrial continental waters, and those measured in the martian fines at the Mars Pathfinder and Viking 1 and 2 landing sites. In particular, the S/Cl ratio in these experiments was about 200, compared with an average value of approx. 5 in martian fines. In contrast, abundance patterns of elements in the brines produced under a present day Mars analog atmosphere were quite similar to those measured in the martian fines at the Mars Pathfinder and Viking 1 and 2 landing sites. This suggests that salts present in the martian regolith may have formed over time as a result of the interaction of surface or subsurface liquid water with basalts in the presence of a martian atmosphere similar in composition to that of today, rather than in an atmosphere higher in acidic volatiles.

Bullock, M. A.↗
NASA NTRS1999

Martian soil component in impact glasses in a Martian meteorite

Chemical compositions of impact melt glass veins, called Lithology C (Lith C) in Martian meteorite EET79001 were determined by electron microprobe analysis. A large enrichment of S, and significant enrichments of Al, Ca, and Na were observed in Lith C glass compared to Lithology A (Lith A). The S enrichment is due to mixing of plagioclase- enriched Lith A material with Martian soil, either prior to or during impact on Mars. A mixture of 87% Lith A, 7% plagioclase, and 6% Martian soil reproduces the average elemental abundances observed in Lith C. Shock melting of such a mixture of plagioclase-enriched, fine-grained Lith A host rock and Martian soil could yield large excesses of S (observed in this study) and Martian atmospheric noble gases (found by Bogard et al., 1983) in Lith C. These mixing proportions can be used to constrain the elemental abundance of phosphorus in Martian soil.

NASA Center JSC↗
NASA NTRS2010

Reduced Martian Carbon: Evidence from Martian Meteorites

Identification of indigenous reduced carbon species on Mars has been a challenge since the first hypotheses about life on Mars were proposed. Ranging from the early astronomical measurements to analyses of samples from the Martian surface in the form of Martian meteorites. The first direct attempt to analyze the carbon species on the surface was in 1976 with the Viking GC-MS in-situ experiment which gave inconclusive results at two sites on Mars [1]. With the recognition in 1983 that samples of the Martian surface were already present on Earth in the form of Martian meteorites by Bogard and Johnson [2] new opportunities became available for direct study of Mars's samples in te rlraesbtrioalratories. Carbon isotopic compositional information suggested a reduced carbon component was present in the Martian meteorites [3-5]. Polycyclic aromatic hydrocarbons associated with carbonate globules in ALH84001 were later identified [6,7]. Jull et al [8] noted that an insoluble component was present within Nakhla and more than 75% of its C lacked any 14C, which is modern-day carbon contaminant. This carbon fraction was believed to be either indigenous (i..e. Martian) or ancient meteoritic carbon phase. Within the fractures of Nakhla and ALH84001, Fisk et al [9,10] identified reduced carbon-enriched areas. Gibson et al. [11] using a combination of NanoSIMS, Focused Electron microscopy, Laser Raman Spectroscopy and Stepped-Combustion Static Mass Spectrometry analyses the presence of possible indigenous reduced carbon components within the 1.3 Ga old Nakhla.

Gibson, Everett K.↗
NASA NTRS2004

Chemical Weathering Records of Martian Soils Preserved in the Martian Meteorite EET79001

Impact-melt glasses, rich in Martian atmospheric gases, contain Martian soil fines (MSF) mixed with other coarse-grained regolith fractions which are produced during impact bombardment on Mars surface. An important characteristic of the MSF fraction is the simultaneous enrichment of felsic component accompanied by the depletion of mafic component relative to the host phase in these glasses. In addition, these glasses yield large sulfur abundances due to the occurrence of secondary mineral phases such as sulfates produced during acid-sulfate weathering of the regolith material near the Martian surface. Sulfurous gases released into atmosphere by volcanoes on Mars are oxidized to H2SO4 which deposit back on the surface of Mars as aerosol particles. Depending on the water availability, sulfuric acids dissolve into solutions which aggressively decompose the Fe-Mg silicates in the Martian regolith. During chemical weathering, structural elements such as Fe, Mg and Ca (among others) are released into the transgressing solutions. These solutions leach away the soluble components of Mg, Ca and Na, leaving behind insoluble iron as Fe3(+) hydroxysulfate mixed with poorly crystalline hydroxide- precipitates under oxidizing conditions. In this study, we focus on the elemental distribution of FeO and SO3 in the glass veins of EET79001, 507 sample, determined by Electron Microprobe and FE SEM measurements at JSC. This glass sample is an aliquot of a bigger glass inclusion ,104 analysed by where large concentrations of Martian atmospheric noble gases are found.

Rao, M. N.↗
NASA NTRS2006

Martian Meteorite Ages and Implications for Martian Cratering History

New radiometrically determined ages of Martian meteorites add to the growing number with crystallization ages <~ 1.4 Ga. The observation of mainly geologically young ages for the Martian meteorites, the only exception being the ~4.5 Ga ALH84001 [1], is paradoxical when viewed in context of a Martian surface thought to be mostly much older as inferred from the surface density of meteorite craters [2]. There appears to be at least a twofold difference between the observed ages of Martian meteorites and their expected ages as inferred from the ages of Martian surfaces obtained from crater densities.

Nyquist, Laurence E.↗
NASA NTRS2017

Ne-20/Ne-22 in the Martian Atmosphere: New Evidence from Martian Meteorites

Analyses of Ne trapped in "pods" of impact melt in the Elephant Moraine 79001 (EET 79001) Martian meteorite led to suggest (Ne-20/Ne-22) approx.10 in the Martian atmosphere (MA). In contrast, obtained trapped (Ne-20/Ne-22)Tr approx.7 from an impact melt vein in Yamato 793605 (Y-793605) and concluded that the isotopic composition of Martian Ne remained poorly defined. A "pyroxene-rich" separate from Dhofar 378 (Dho 378) analyzed gave a comparatively high trapped Ne concentration and (Ne-20/Ne-22) = 7.3+/-0.2 in agreement with the Y-793605 value. We explore the hypothesis that Martian Ne was trapped in the Dho 378 meteorite in a manner similar to entrapment of terrestrial Ne in tektites strengthening the "Martian atmosphere" interpretation. We also report new data for Northwest Africa 7034 (NWA 7034) that are consistent with the Ne data for Dho 378.

Park, J.↗
NASA NTRS1988

Samples from Martian craters: Origin of the Martian soil by hydrothermal alteration of impact melt deposits and atmospheric interactions with ejecta during crater formation

The origin of the Martian soil is an important question for understanding weathering processes on the Martian surface, and also for understanding the global geochemistry of Mars. Chemical analyses of the soil will provide an opportunity to examine what may be a crustal average, as studies of loess on the Earth have demonstrated. In this regard the origin of the Martian soil is also important for understanding the chemical fractionations that have affected the composition of the soil. Several processes that are likely to contribute to the Martian soil are examined.

Newsom, Horton E.↗
NASA NTRS2007

Identification of Iron-Bearing Phases on the Martian Surface and in Martian Meteorites and Analogue Samples by Moessbauer Spectroscopy

The Moessbauer spectrometers on the Mars Exploration Rovers (MER) Spirit (Gusev Crater) and Opportunity (Meridiani Planum) have each analyzed more than 100 targets during their ongoing missions (>1050 sols). Here we summarize the Fe-bearing phases identified to date and compare the results to Moessbauer analyses of martian meteorites and lunar samples. We use lunar samples as martian analogues because some, particularly the low-Ti Apollo 15 mare basalts, have bulk chemical compositions that are comparable to basaltic martian meteorites [1,2]. The lunar samples also provide a way to study pigeonite-rich samples. Pigeonite is a pyroxene that is not common in terrestrial basalts, but does often occur on the Moon and is present in basaltic martian meteorites

Klingelhoefer, G.↗
NASA NTRS2009

Isotopic Evidence for a Martian Regolith Component in Martian Meteorites

Noble gas measurements in gas-rich impact-melt (GRIM) glasses in EET79001 shergottite showed that their elemental and isotopic composition is similar to that of the Martian atmosphere [1-3]. The GRIM glasses contain large amounts of Martian atmospheric gases. Those measurements further suggested that the Kr isotopic composition of Martian atmosphere is approximately similar to that of solar Kr. The (80)Kr(sub n) - (80)Kr(sub M) mixing ratio in the Martian atmosphere reported here is approximately 3%. These neutron-capture reactions presumably occurred in the glass-precursor regolith materials containing Sm- and Br- bearing mineral phases near the EET79001/ Shergotty sites on Mars. The irradiated materials were mobilized into host rock voids either during shock-melting or possibly by earlier aeolian / fluvial activity.

Rao, M. N.↗
NASA NTRS1974

Data processing of Martian topographic information obtained from ground-based radar and spectroscopy and from Mariners 6 and 7. Martian topography elevations: Data processing

Papers are presented which were published as a result of a project involving the preparation of a topographical elevation contour map of Mars from all data sources available through 1969, as well as the observation of Mars by spectroscopic methods in 1971 to provide additional pressure data for topographic information. Topics of the papers include: the analysis of large-scale Martian topography variations - data preparation from earth based radar, earth based CO2 spectroscopy, and Mariners 6 and 7 CO2 spectroscopy; the analysis of water content in observed Martian white clouds; and Martian, lunar, and terrestrial crusts - a three-dimensional exercise in comparative geophysics.

Anderson, K. A.↗
NASA NTRS1978

Martian cratering V - Toward an empirical Martian chronology, and its implications

This paper estimates ages of Martian features by dividing least-square-fitted crater densities by an estimated Martian crater production rate. This method is more rigorous than methods based purely on assumptions about correspondence of lunar and Martian cratering rates. Results are interpreted as supporting the conclusion of Burns et al (in press) that Mars shifted climatic states due to a change in obliguity caused by buildup of massive volcanics. Prior to a few gy. ago, conditions favored erosion, deposition, and fluvial channel formation. Recent volcanics postdate this era, and the surfaces of the major shields are fairly well constrained in age to a few hundred my, in agreement with Masursky et al.

Hartmann, W. K.↗
NASA NTRS1992

In situ identification of the Martian surface material and its interaction with the Martian atmosphere using DTA/GC

Little is known about the mineralogy of the martian surface material. Several techniques have been suggested as candidates for the in situ identification of the martian surface material. The most promising of these techniques include differential thermal analysis (DTA) coupled with gas chromatography (GC) and differential scanning calorimetry (DSC) coupled with either mass spectrometry (MS) or GC. Our studies showed that differential thermal analysis coupled with gas chromatography (DTA/GC) is a more appropriate analytical technique than DSC/MS or DSC/GC to identify the mineralogy of the martian surface material in situ. DTA/GC can be regarded as an advancement from pyrolytic GC analyses that were successfully flown on previous missions, but have supplied only limited mineralogical information.

Mancinelli, R. L.↗
NASA NTRS1999

Magnetometer Data Tests Models for the Origin of the Martian Crustal Dichotomy; Dichotomy Models Constrain Timing of Martian Magnetic Field

Measurements recently supplied by the MGS Magnetometer/Electron Reflectometer (MAG/ER) on MGS can be applied to test theories of the origin of the martian crustal dichotomy. Strong (+/- 1500 nT) magnetic anomalies are observed in the Martian crust. The observations can be summarized as follows: 1) strong crustal magnetic sources are generally confined to the southern highlands, although weaker (approx. 40 nT) anomalies were observed during close periapsis; 2) strong magnetic anomalies are absent in the vicinity of Hellas and Argyre; 3) the anomalies in the region 0 deg to 90 deg S, 120 deg to 240 deg west have a linear geometry, strike generally east west for 1000s km, and show several reversals. This latter point has led to the suggestion that some form of lateral plate tectonics may have been operative in the southern highlands of Mars. These observations have led previous workers to hypothesize that the magnetic anomalies were present prior to and were destroyed by the formation of Hellas and Argyre. As such large impacts are confined to the era of heavy bombardment, this places the time of formation of large magnetic anomalies prior to approx. 3.9 Ga. One obvious extension of this is that the northern lowlands lack significant anomalies because they were erased by impacts and/or the northern lowlands represent crust completely reheated above the Curie temperature. Preliminary observations of the distributions of the large crustal magnetic anomalies show that many of them extend continuously over the highland lowland boundary. This occurs particularly north of the boundary between 30 deg W and 270 deg W, corresponding to northern Arabia, but also occurs in southern Elysium (approx. 10 deg S, 200 deg) and the SW portion of Tharsis (approx. 15 deg S, 140 deg). This suggests that, in these areas, Noachian crust containing the greater than 3.9 Ga magnetic signature, lies beneath the northern highlands. This geometry can be used to test models for the formation of the martian crustal dichotomy. Additional information is contained in the original extended abstract.

Gilmore, M. S.↗
NASA NTRS2012

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.↗