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Gooding, J. L.

Publications and source records attributed to Gooding, J. L..

At least 19 records

Thermal Analyzer for Planetary Soil (TAPS): an in Situ Instrument for Mineral and Volatile-element Measurements

Thermal Analyzer for Planetary Soil (TAPS) offers a specific implementation for the generic thermal analyzer/evolved-gas analyzer (TA/EGA) function included in the Mars Environmental Survey (MESUR) strawman payload; applications to asteroids and comets are also possible. The baseline TAPS is a single-sample differential scanning calorimeter (DSC), backed by a capacitive-polymer humidity sensor, with an integrated sampling mechanism. After placement on a planetary surface, TAPS acquires 10-50 mg of soil or sediment and heats the sample from ambient temperature to 1000-1300 K. During heating, DSC data are taken for the solid and evolved gases are swept past the water sensor. Through ground based data analysis, multicomponent DSC data are deconvolved and correlated with the water release profile to quantitatively determine the types and relative proportions of volatile-bearing minerals such as clays and other hydrates, carbonates, and nitrates. The rapid-response humidity sensors also achieve quantitative analysis of total water. After conclusion of soil-analysis operations, the humidity sensors become available for meteorology. The baseline design fits within a circular-cylindrical volume less than 1000 cm(sup 3), occupies 1.2 kg mass, and consumes about 2 Whr of power per analysis. Enhanced designs would acquire and analyze multiple samples and employ additional microchemical sensors for analysis of CO2, SO2, NO(x), and other gaseous species. Atmospheric pumps are also being considered as alternatives to pressurized purge gas.

Gooding, J. L.

Calorimetric thermometry of meteoritic troilite: A feasibility study

Two solid-state phase transitions in troilite (FeS) can be readily measured by differential scanning calorimetry (DSC) on samples of only a few milligrams. Troilite from the Mundrabilla iron meteorite displays a DSC fingerprint which is distinct from that of terrestrial troilite from Del Norte Co., California; their response to subsequent heating also differ significantly. Further work may establish whether troilite thermometry of meteorites is possible using DSC.

Allton, J. H.

Geochemistry and setting of Martian weathering: The Lafayette meteorite

Lafayette, one of the SNC (martian) meteorites, contains preterrestrial alteration materials rich in smectite and ferric oxides. The compositions and textures of the veinlets suggest that they were formed in episodic alteration events by waters that contained a relatively small load of dissolved salts. The Lafayette achondrite, one of the nakhlites of probable martian origin, is an igneous rock consisting mostly of augite and olivine, with interstitial feldspar, sulfides (pyrite), high-Si glass, and other phases. Like Nakhla itself, Lafayette contains veinlets of hydrous alteration materials. We studied thin sections of sample ME2116 (Field Museum, Chicago), using scanning and transmission electron microscopy (SEM and TEM) with energy dispersive X-ray spectrometry (EDS).

Treiman, A. H.

Aqueous-alteration products in S-N-C meteorites and implications for volatile/regolith interactions on Mars

The shergottite, nakhlite, and Chassigny (SNC) meteorites are inferred to be samples from the Martian surface, and so provide a wealth of information on Martian petrology and geochemistry. Because the SNCs are igneous rocks, it has not been obvious that they could reveal much about low-temperature geochemical processes and atmosphere surface interactions on Mars. However, five of the eight SNCs are known to contain low-temperature hydrous minerals and related phase of likely martian origin. Here, we review these martian weathering and alteration products in SNCs and outline possible implications for volatile/regolith interactions and regolith sinks for volatiles on Mars.

Treiman, A. H.

The case for planetary sample return missions. 2. History of Mars

Principal science goals for exploration of Mars are to establish the chemical, isotopic, and physical state of Martian material, the nature of major surface-forming processes and their time scales, and the past and present biological potential of the planet. Many of those goals can only be met by detailed analyses of atmospheric gases and carefully selected samples of fresh rocks, weathered rocks, soils, sediments, and ices. The high-fidelity mineral separations, complex chemical treatments, and ultrasensitive instrument systems required for key measurements, as well as the need to adapt analytical strategies to unanticipated results, point to Earth-based laboratory analyses on returned Martian samples as the best means for meeting the stated objectives.

NASA Center ARC

Mineralogical sinks for biogenic elements on Mars

The efficacy of biochemical reactions on Mars should depend not only on concentrations of the biogenic elements H, C, N, O, and S but also on the forms (compounds and water-souble ions) that are available to those elements. It is possible that mineralogical reactions could act to lock biogenic elements into relatively inaccessible inorganic forms or, alternatively, to shelter sensitive organic compounds from chemically hostile environments. Recognition of these competing pathways is essential in planning sampling mission and in situ experiments directed toward assessing the biological potential of Mars.

Gooding, J. L.

Rapid growth of magnesium-carbonate weathering products in a stony meteorite from Antarctica

Nesquehonite, a hydrous magnesium carbonate, occurs as a weathering product on the surface of the Antarctic meteorite LEW 85320 (H5 chondrite). Isotopic measurements of delta(C-13) and delta(O-18) indicate that the nesquehonite formed at near freezing temperatures by reaction of meteoritic minerals with terrestrial water and carbon dioxide. Results from carbon-14 dating suggest that, although the meteorite has been in Antarctica for at least 32,000 to 33,000 years, the nesquehonite formed after AD 1950.

Jull, A. J. T.

Martian weathering products as tracers of climate change and atmosphere/hydrosphere evolution on Mars

Primary objectives for exploration of Mars include determination of: (1) the distribution, abundance, and sources and sinks of volatile materials, and (2) the interaction of surface materials with the atmosphere. Both objectives fall within the purview of planetary surface weathering studies and require documented samples of weathered materials, including rock surfaces, soils, and sediments. Major issues to be addressed in selecting and studying Martian samples in this context are summarized.

Gooding, J. L.

Zeolites on Mars: Possible environmental indicators in soils and sediments

Weathering products should serve as indicators of weathering environments and may provide the best evidence of the nature of climate change on Mars. No direct mineralogical measurements of Martian regolith were performed by the Viking missions, but the biology and X-ray fluorescence experiments provided some information on the physiochemical properties of Martian regolith. Most post-Viking studies of candidate weathering products have emphasized phyllosilicates and Fe-oxides; zeolites are potentially important, but overlooked, candidate Martian minerals. Zeolites would be important on Mars for three different reasons. First, they are major sinks of atmospheric gases and, per unit mass, are stronger and more efficient sorbents than are phyllosilicates. Secondly, they can be virtually unique sorbents and shelters for organic compounds and possible catalysts for organic-based reactions. Finally, their exchangeable ions are good indicators of the chemical properties of solutions with which they have communicated. Accordingly, the search for information on past compositions of the Martian atmosphere and hydrosphere should find zeolites to be rich repositories.

Ming, D. W.

Computer modeling of the mineralogy of the Martian surface, as modified by aqueous alteration

Mineralogical constraints can be placed on the Martian surface by assuming chemical equilibria among the surface rocks, atmosphere and hypothesized percolating groundwater. A study was made of possible Martian surface mineralogy, as modified by the action of aqueous alteration, using the EQ3/6 computer codes. These codes calculate gas fugacities, aqueous speciation, ionic strength, pH, Eh and concentration and degree of mineral saturation for complex aqueous systems. Thus, these codes are also able to consider mineralogical solid solutions. These codes are able to predict the likely alteration phases which will occur as the result of weathering on the Martian surface. Knowledge of the stability conditions of these phases will then assist in the definition of the specifications for the sample canister of the proposed Martian sample return mission. The model and its results are discussed.

Zolensky, M. E.

Calcium carbonate and calcium sulfate in Martian meteorite EETA79001

Chips of glassy Lithology C of EETA79001 were studied by scanning electron microscopy and energy dispersive X-ray spectroscopy to determine the mineralogy and petrogenesis of the glass that was shown by others to contain trapped Mars-like gases. Calcium carbonite was identified as massive to acicular crystals for which Ca, C, and O were the major elements. Calcium sulfate was identified as prismatic-acicular crystals with Ca and S as the major elements.

Gooding, J. L.

Non-equilibrium freezing of water-ice in sandy basaltic regoliths and implications for fluidized debris flows on Mars

Many geomorphic features on Mars were attributed to Earth-analogous, cold-climate processes involving movement of water or ice lubricated debris. Clearly, knowledge of the behavior of water in regolith materials under Martian conditions is essential to understanding the postulated geomorphic processes. Experiments were performed with sand-sized samples of natural basaltic regoliths in order to further elucidate how water/regolith interactions depend upon grain size and mineralogy. The data reveal important contrasts with data for clay-mineral substrates and suggest that the microphysics of water/mineral interactions might affect Martian geomorphic processes in ways that are not fully appreciated. Sand and silt sized fractions of two soils from the summit of Mauna Kea were used as Mars-analogous regolith materials. Temperatures were measured for water/ice phase transitions as wet slurries of individual soil fractions which were cooled or heated at controlled rates under a carbon dioxide atmosphere. Freezing and melting of ice was studied as a function of water/soil mass ratio, soil particle size, and thermal-cycle rate. Comparison tests were done under the same conditions with U.S. Geological Survey standard rock powders.

Gooding, J. L.

Aqueous alteration in S-N-C meteorites and implications for weathering products on Mars

Is shergottite, nakhlite, and chassignite (SNC) meteorites are rocks propelled to earth by large meteoroid impacts on Mars, then it is possible to deduce much about Martian igneous petrology and geochemistry. Because SNCs are igneous rocks, however, it was not obvious that they could reveal much about sedimentary and soil petrology and low-temperature geochemistry of Mars. It is important, though, that at least four of eight SNCs carry evidence for low-temperature, extraterrestrial weathering product phases. Evidence is reviewed for Martian weathering and alteration products in SNCs and possible inferences for volatile/regolith interactions, regolith mineralogy, and sinks for the putative hidden volatiles on Mars are outlined.

Gooding, J. L.

Antarctic Meteorite Newsletter, volume 9, no. 2

Preliminary description and classifications of meteorites that were completed since publication of the February issue are contained. Most large (greater than 150 g) specimens (regardless of petrologic type) and all pebble sized (less than 150 g) specimens of special petrologic type are represented by separate descriptions. However, specimens of nonspecial petrologic type are listed only as single line entries. For convenience, new specimens are also recast by petrologic type. Each macroscopic description summarizes features that were visible to the eye at the time the meteorite was first examined. Classification is based on microscopic petrography and resonnaissance-level electron-probe microanalysis. The pairing list was updated.

Gooding, J. L.

Martian volatiles in shergottite EETA 79001 - New evidence from oxidized sulfur and sulfur-rich aluminosilicates

Two equivalent chips of lithology A (lith-A) and lithology C (lith-C) taken from the same interior portion of EETA 79001 shergottite have been analyzed for volatile species produced by high-vacuum pyrolysis. The lith-C was found to contain an oxidized sulfur component that does not occur in lith-A. The preterrestrial origin of this component in lith-C is supported by the occurrence in lith-C of sulfur- and chlorine-rich aluminosilicates that are not the same as Antarctic weathering products found in the control samples. The oxidation state and distribution of sulfur found in lith-C are consistent with the interpretation of EETA 79001 as a rock from Mars.

Gooding, J. L.

Martian dust particles as condensation nuclei - A preliminary assessment of mineralogical factors

Experiments were performed to determine the factors influencing ice nucleation detected in Viking Lander data from the Mars surface. The study focused on the relationship between mineral properties and condensate formation under Mars conditions. Pulverized particles of the primary phases of basaltic rocks and their alteration products, expandable clay minerals and a nonexpandable clay mineral, and petrologically well-characterized regolith materials ranging from 10-60 microns in size, were studied. The powders were individually or in combinations mixed with water in a flowing CO2 atmosphere while calorimetry data was taken on the ice nucleation threshold. The ice-forming characteristics of the mixes were found to be a function of the crystallographic disregistry, chemical bonding, and active-site properties of the individual minerals. The crystalline materials were better nucleators of condensates than were the cryptocrystalline mineral specimens, while nonexpandable clay materials, particularly zeolite, were the more effective nucleators among the weathering product materials.

Gooding, J. L.

Weathering of stony meteorites in Antarctica

Weathering produces undesirable physical, chemical, and isotopic changes that might disturb the records of cosmochemical evolution that are sought in meteorites. Meteorites are physically disintegrated by crack propagation phenomena, including ice riving and secondary mineral riving, and are probably abraded by wind that is laden with ice crystals or dust particles. Chemical weathering proceeds by oxidation, hydration, carbonation, and solution and produces a variety of secondary minerals and mineraloids. Differential weathering under freezing conditions is discussed, as well as, the mineralogy of weathering products. Furthermore, the use of Antarctic alteration of meteorites could be used as an excellent analog for weathering on Mars or on cometary bodies.

Gooding, J. L.

Planetary surface weathering

The weathering of planetary surfaces is treated. Both physical and chemical weathering (reactions between minerals or mineraloids and planetary volatiles through oxidation, hydration, carbonation, or solution processes) are discussed. Venus, earth, and Mars all possess permanent atmospheres such that weathering should be expected to significantly affect their respective surfaces. In contrast, Mercury and the moon lack permanent atmospheres but conceivably could experience surface weathering in response to transient atmospheres generated by volcanic or impact cratering events. Weathering processes can be postulated for other rocky objects including Io, Titan, asteroids, and comets.

Gooding, J. L.