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Roger N Clark - One of the best experts on this subject based on the ideXlab platform.
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identification of a basaltic component on the martian surface from thermal emission spectrometer data
Journal of Geophysical Research, 2000Co-Authors: Philip R Christensen, J L Bandfield, Michael D Smith, Victoria E Hamilton, Roger N ClarkAbstract:The Mars Global Surveyor Thermal Emission Spectrometer (TES) instrument collected 4.8×106 spectra of Mars during the initial aerobraking and science-phasing periods of the mission (September 14, 1997, through April 29, 1998). Two previously developed atmosphere-removal models were applied to data from Cimmeria Terra (25°S, 213°W). The surface spectra derived for these two models agree well, indicating that the surface and atmosphere emission can be separated and that the exact atmosphere-removal model used has little effect on the derived surface composition. The Cimmeria spectra do not match terrestrial high-silica igneous rocks (granite and rhyolite), ultramafic igneous rocks, limestone, or quartz- and clay-rich sandstone and siltstone. A particulate (sand-sized) sample of terrestrial flood basalt does provide an excellent match in both spectral shape and band depth to the Cimmeria spectrum over the entire TES spectral range. No unusual particle size effects are required to account for the observed spectral shape and depth. The implied grain size is consistent with the thermal inertia and albedo of this region, which indicate a sand-sized surface with little dust. The identification of basalt is consistent with previous indications of pyroxene and basalt-like compositions from visible/near-infrared and thermal-infrared spectral measurements. A linear spectral deconvolution model was applied to both surface-only Cimmeria spectra using a library of 60 minerals to determine the composition and abundance of the component minerals. Plagioclase feldspar (45%; 53%) and clinopyroxene (26%; 19%) were positively identified above an estimated detection threshold of 10–15% for these minerals. The TES observations provide the first identification of feldspars on Mars. The best fit to the Mars data includes only clinopyroxene compositions; no orthopyroxene compositions are required to match the Cimmeria spectra. Olivine (12%; 12%) and sheet silicate (15%; 11%) were identified with lower confidence. Carbonates, quartz, and sulfates were not identified in Cimmeria at detection limits of ∼5, 5, and 10%, respectively. Their presence elsewhere, however, remains open. The Cimmeria spectra are not well matched by any one SNC Meteorite spectrum, indicating that this region is not characterized by a single SNC lithology. The occurrence of unweathered feldspar and pyroxene in Cimmeria, together with the inferred presence of pyroxene and unweathered basalts in other dark regions and at the Viking and Pathfinder landing sites, provides evidence that extensive global chemical weathering of materials currently exposed on the Martian surface has not occurred.
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identification of a basaltic component on the martian surface from thermal emission spectrometer data
Journal of Geophysical Research, 2000Co-Authors: Philip R Christensen, J L Bandfield, Michael D Smith, Victoria E Hamilton, Roger N ClarkAbstract:The Mars Global Surveyor Thermal Emission Spectrometer (TES) instrument collected 4.8×106 spectra of Mars during the initial aerobraking and science-phasing periods of the mission (September 14, 1997, through April 29, 1998). Two previously developed atmosphere-removal models were applied to data from Cimmeria Terra (25°S, 213°W). The surface spectra derived for these two models agree well, indicating that the surface and atmosphere emission can be separated and that the exact atmosphere-removal model used has little effect on the derived surface composition. The Cimmeria spectra do not match terrestrial high-silica igneous rocks (granite and rhyolite), ultramafic igneous rocks, limestone, or quartz- and clay-rich sandstone and siltstone. A particulate (sand-sized) sample of terrestrial flood basalt does provide an excellent match in both spectral shape and band depth to the Cimmeria spectrum over the entire TES spectral range. No unusual particle size effects are required to account for the observed spectral shape and depth. The implied grain size is consistent with the thermal inertia and albedo of this region, which indicate a sand-sized surface with little dust. The identification of basalt is consistent with previous indications of pyroxene and basalt-like compositions from visible/near-infrared and thermal-infrared spectral measurements. A linear spectral deconvolution model was applied to both surface-only Cimmeria spectra using a library of 60 minerals to determine the composition and abundance of the component minerals. Plagioclase feldspar (45%; 53%) and clinopyroxene (26%; 19%) were positively identified above an estimated detection threshold of 10–15% for these minerals. The TES observations provide the first identification of feldspars on Mars. The best fit to the Mars data includes only clinopyroxene compositions; no orthopyroxene compositions are required to match the Cimmeria spectra. Olivine (12%; 12%) and sheet silicate (15%; 11%) were identified with lower confidence. Carbonates, quartz, and sulfates were not identified in Cimmeria at detection limits of ∼5, 5, and 10%, respectively. Their presence elsewhere, however, remains open. The Cimmeria spectra are not well matched by any one SNC Meteorite spectrum, indicating that this region is not characterized by a single SNC lithology. The occurrence of unweathered feldspar and pyroxene in Cimmeria, together with the inferred presence of pyroxene and unweathered basalts in other dark regions and at the Viking and Pathfinder landing sites, provides evidence that extensive global chemical weathering of materials currently exposed on the Martian surface has not occurred.
Philip R Christensen - One of the best experts on this subject based on the ideXlab platform.
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identification of a basaltic component on the martian surface from thermal emission spectrometer data
Journal of Geophysical Research, 2000Co-Authors: Philip R Christensen, J L Bandfield, Michael D Smith, Victoria E Hamilton, Roger N ClarkAbstract:The Mars Global Surveyor Thermal Emission Spectrometer (TES) instrument collected 4.8×106 spectra of Mars during the initial aerobraking and science-phasing periods of the mission (September 14, 1997, through April 29, 1998). Two previously developed atmosphere-removal models were applied to data from Cimmeria Terra (25°S, 213°W). The surface spectra derived for these two models agree well, indicating that the surface and atmosphere emission can be separated and that the exact atmosphere-removal model used has little effect on the derived surface composition. The Cimmeria spectra do not match terrestrial high-silica igneous rocks (granite and rhyolite), ultramafic igneous rocks, limestone, or quartz- and clay-rich sandstone and siltstone. A particulate (sand-sized) sample of terrestrial flood basalt does provide an excellent match in both spectral shape and band depth to the Cimmeria spectrum over the entire TES spectral range. No unusual particle size effects are required to account for the observed spectral shape and depth. The implied grain size is consistent with the thermal inertia and albedo of this region, which indicate a sand-sized surface with little dust. The identification of basalt is consistent with previous indications of pyroxene and basalt-like compositions from visible/near-infrared and thermal-infrared spectral measurements. A linear spectral deconvolution model was applied to both surface-only Cimmeria spectra using a library of 60 minerals to determine the composition and abundance of the component minerals. Plagioclase feldspar (45%; 53%) and clinopyroxene (26%; 19%) were positively identified above an estimated detection threshold of 10–15% for these minerals. The TES observations provide the first identification of feldspars on Mars. The best fit to the Mars data includes only clinopyroxene compositions; no orthopyroxene compositions are required to match the Cimmeria spectra. Olivine (12%; 12%) and sheet silicate (15%; 11%) were identified with lower confidence. Carbonates, quartz, and sulfates were not identified in Cimmeria at detection limits of ∼5, 5, and 10%, respectively. Their presence elsewhere, however, remains open. The Cimmeria spectra are not well matched by any one SNC Meteorite spectrum, indicating that this region is not characterized by a single SNC lithology. The occurrence of unweathered feldspar and pyroxene in Cimmeria, together with the inferred presence of pyroxene and unweathered basalts in other dark regions and at the Viking and Pathfinder landing sites, provides evidence that extensive global chemical weathering of materials currently exposed on the Martian surface has not occurred.
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identification of a basaltic component on the martian surface from thermal emission spectrometer data
Journal of Geophysical Research, 2000Co-Authors: Philip R Christensen, J L Bandfield, Michael D Smith, Victoria E Hamilton, Roger N ClarkAbstract:The Mars Global Surveyor Thermal Emission Spectrometer (TES) instrument collected 4.8×106 spectra of Mars during the initial aerobraking and science-phasing periods of the mission (September 14, 1997, through April 29, 1998). Two previously developed atmosphere-removal models were applied to data from Cimmeria Terra (25°S, 213°W). The surface spectra derived for these two models agree well, indicating that the surface and atmosphere emission can be separated and that the exact atmosphere-removal model used has little effect on the derived surface composition. The Cimmeria spectra do not match terrestrial high-silica igneous rocks (granite and rhyolite), ultramafic igneous rocks, limestone, or quartz- and clay-rich sandstone and siltstone. A particulate (sand-sized) sample of terrestrial flood basalt does provide an excellent match in both spectral shape and band depth to the Cimmeria spectrum over the entire TES spectral range. No unusual particle size effects are required to account for the observed spectral shape and depth. The implied grain size is consistent with the thermal inertia and albedo of this region, which indicate a sand-sized surface with little dust. The identification of basalt is consistent with previous indications of pyroxene and basalt-like compositions from visible/near-infrared and thermal-infrared spectral measurements. A linear spectral deconvolution model was applied to both surface-only Cimmeria spectra using a library of 60 minerals to determine the composition and abundance of the component minerals. Plagioclase feldspar (45%; 53%) and clinopyroxene (26%; 19%) were positively identified above an estimated detection threshold of 10–15% for these minerals. The TES observations provide the first identification of feldspars on Mars. The best fit to the Mars data includes only clinopyroxene compositions; no orthopyroxene compositions are required to match the Cimmeria spectra. Olivine (12%; 12%) and sheet silicate (15%; 11%) were identified with lower confidence. Carbonates, quartz, and sulfates were not identified in Cimmeria at detection limits of ∼5, 5, and 10%, respectively. Their presence elsewhere, however, remains open. The Cimmeria spectra are not well matched by any one SNC Meteorite spectrum, indicating that this region is not characterized by a single SNC lithology. The occurrence of unweathered feldspar and pyroxene in Cimmeria, together with the inferred presence of pyroxene and unweathered basalts in other dark regions and at the Viking and Pathfinder landing sites, provides evidence that extensive global chemical weathering of materials currently exposed on the Martian surface has not occurred.
J F Bell - One of the best experts on this subject based on the ideXlab platform.
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mineralogy composition and alteration of mars pathfinder rocks and soils evidence from multispectral elemental and magnetic data on terrestrial analogue SNC Meteorite and pathfinder samples
Journal of Geophysical Research, 2000Co-Authors: Richard V Morris, D C Golden, J F Bell, T D Shelfer, Andreas C Scheinost, Nancy W Hinman, George Furniss, Stanley A Mertzman, J L Bishop, Douglas W MingAbstract:Major element, multispectral, and magnetic properties data were obtained at Ares Vallis during the Mars Pathfinder mission. To understand the compositional, mineralogical, and process implications of these data, we obtained major element, mineralogical, and magnetic data for well-crystalline and nanophase ferric minerals, terrestrial analogue samples with known geologic context, and SNC Meteorites. Analogue samples include unaltered, palagonitic, and sulfatetic tephra from Mauna Kea Volcano (hydrolytic and acid-sulfate alteration), steam vent material from Kilauea Volcano (hydrolytic alteration), and impactites from Meteor Crater (relithification). Salient results for Mars Pathfinder include: (1) Band depths BD530b and BD600 and the reflectivity ratio R800/R750 are consistent with the dominant ferric mineral being nanophase ferric oxide associated with an unknown amount of H2O and occurring in composite particles along with subordinate amounts of other ferric minerals. Hematite and hematite plus nanophase goethite are most consistent with the data, but maghemite, akaganeite, schwertmannite, and nanophase lepidocrocite are also possible interpretations. Ferric oxides that are consistently not favored by the data as sole alteration products are jarosites and well-crystalline goethite and lepidocrocite. (2) The strength of the ferric adsorption edge (R750/R445) implies the Fe3+/Fe2+ values for Pathfinder rock and soil are within the ranges 0.7–3 and 3–20, respectively. (3) Ferrous silicates are indicated for subsets of Pathfinder rocks and soils. One subset has a band minimum near 930 nm that can attributed to low-Ca pyroxene. Alternatively, the band could be a second manifestation of certain ferric oxides, including nanophase goethite, maghemite, akaganeite, and schwertmannite. Another subset has a negative spectral slope from ∼800 to 1005 nm which could result from the high-energy wing of a high-Ca pyroxene and/or olivine band, a mixture of bright and dark materials, and, for rocks, thin coatings of bright dust on dark rocks. (4) Chemical data on Pathfinder rocks and soils are consistent with two-component mixtures between an “andesitic” rock with low MgO and SO3 concentrations (soil-free rock) and a global, basaltic soil with high MgO and SO3 concentrations (rock-free soil). Pathfinder rock-free soil can be modeled as a chemical mixture of SNC Meteorites and the Pathfinder soil-free rock. (5) Pathfinder soil cannot be obtained by chemical alteration of Pathfinder rocks by any of the hydrolytic and acid-sulfate alteration processes we studied. Presumably, global mixing has obscured and possibly erased the elemental signatures of chemical alteration. (6) The strongly magnetic phase in palagonitic and sulfatetic tephra is titanomagnetite and possibly its oxidation product titanomaghemite (Fe-Ti spinels). The saturation magnetization of the tephra samples (0.5–2.0 Am2/kg) is at or below the low end of the range inferred for Martian dust (4±2 Am2/kg), implying that lithogenic Fe-Ti spinels are a possible candidate for the Martian strongly magnetic phase. (7) The predominantly palagonitic spectral signature and magnetic nature of Martian soil and dust are consistent with glassy precursors with imbedded Fe-Ti spinel particles. Comparison with lunar glass production rates suggests that production of sufficient quantities of glassy materials on Mars by volcanic and impact processes is sufficient to account for these observations.
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mineralogic and compositional properties of martian soil and dust results from mars pathfinder
Journal of Geophysical Research, 2000Co-Authors: J F Bell, Richard V Morris, H Y Mcsween, J A Crisp, S L Murchie, N T Bridges, J R Johnson, D T Britt, M P Golombek, H J MooreAbstract:Mars Pathfinder obtained multispectral, elemental, magnetic, and physical measurements of soil and dust at the Sagan Memorial Station during the course of its 83 sol mission. We describe initial results from these measurements, concentrating on multispectral and elemental data, and use these data, along with previous Viking, SNC Meteorite, and telescopic results, to help constrain the origin and evolution of Martian soil and dust. We find that soils and dust can be divided into at least eight distinct spectral units, based on parameterization of Imager for Mars Pathfinder (IMP) 400 to 1000 nm multispectral images. The most distinctive spectral parameters for soils and dust are the reflectivity in the red, the red/blue reflectivity ratio, the near-IR spectral slope, and the strength of the 800 to 1000 nm absorption feature. Most of the Pathfinder spectra are consistent with the presence of poorly crystalline or nanophase ferric oxide(s), sometimes mixed with small but varying degrees of well-crystalline ferric and ferrous phases. Darker soil units appear to be coarser-grained, compacted, and/or mixed with a larger amount of dark ferrous materials relative to bright soils. Nanophase goethite, akaganeite, schwertmannite, and maghemite are leading candidates for the origin of the absorption centered near 900 nm in IMP spectra. The ferrous component in the soil cannot be well-constrained based on IMP data. Alpha proton X-ray spectrometer (APXS) measurements of six soil units show little variability within the landing site and show remarkable overall similarity to the average Viking-derived soil elemental composition. Differences exist between Viking and Pathfinder soils, however, including significantly higher S and Cl abundances and lower Si abundances in Viking soils and the lack of a correlation between Ti and Fe in Pathfinder soils. No significant linear correlations were observed between IMP spectral properties and APXS elemental chemistry. Attempts at constraining the mineralogy of soils and dust using normative calculations involving mixtures of smectites and silicate and oxide minerals did not yield physically acceptable solutions. We attempted to use the Pathfinder results to constrain a number of putative soil and dust formation scenarios, including palagonitization and acid-fog weathering. While the Pathfinder soils cannot be chemically linked to the Pathfinder rocks by palagonitization, this study and McSween et al. [1999] suggest that palagonitic alteration of a Martian basaltic rock, plus mixture with a minor component of locally derived andesitic rock fragments, could be consistent with the observed soil APXS and IMP properties.
Richard V Morris - One of the best experts on this subject based on the ideXlab platform.
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mineralogy of SNC Meteorite eet 79001 by simultaneous fitting of mossbauer backscatter spectra
Lunar and Planetary Science Conference, 2010Co-Authors: David G Agresti, Richard V MorrisAbstract:Introduction: We have acquired Mossbauer spectra for SNC Meteorite EET79001 with a MIMOS II backscatter Mossbauer spectrometer [1] similar to those now operating on Mars as part of the Mars Exploration Rover (MER) missions. We are working to compare the Fe mineralogical composition of martian Meteorites with in-situ measurements on Mars. Our samples were hand picked from the >1 mm size fraction of saw fines on the basis of lithology, color, and grain size (Table 1). The chips were individually analyzed at ~300K by placing them on a piece of plastic that was in turn supported by the contact ring of the instrument (oriented vertically). Tungsten foil was used to mask certain areas from analysis. As shown in Figure 1, a variety of spectra was obtained, each resulting from different relative contributions of the Fe-bearing minerals present in the sample. Because the nine samples are reasonably mixtures of the same Fe-bearing phases in variable proportions, the nine spectra were fit simultaneously (simfit) with a common model, adjusting parameters to a single minimum chi-squared convergence criterion [2]. The starting point for the fitting model and values of hyperfine parameters was the work of Solberg and Burns [3], who identified olivine, pyroxene, and ferrous glass as major, and ilmenite and a ferric phase as minor ( 1 mm chips) of EET79001,N studied in this work. a ID b N Appearance; Processing A 65 Selected light green clasts B 65 Selected light green clasts C 65 Lithology C D 12 Grey chip E 65 Lithology C F 12 Black chips (fusion crust) G 12 Black side of grey chip (fusion crust) H 65 Grey chip with large clast I 65 Coarse-grained grey chip a Sample sequence identifier b Saw fine identifier
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mineralogy of SNC Meteorite eet79001 by simultaneous fitting of moessbauer backscatter spectra
Lunar and Planetary Science Conference, 2010Co-Authors: Richard V Morris, David G AgrestiAbstract:We have acquired M ssbauer spectra for SNC Meteorite EET79001 with a MIMOS II backscatter M ssbauer spectrometer [1] similar to those now operating on Mars as part of the Mars Exploration Rover (MER) missions. We are working to compare the Fe mineralogical composition of martian Meteorites with in-situ measurements on Mars. Our samples were hand picked from the >1 mm size fraction of saw fines on the basis of lithology, color, and grain size (Table 1). The chips were individually analyzed at approx.300K by placing them on a piece of plastic that was in turn supported by the contact ring of the instrument (oriented vertically). Tungsten foil was used to mask certain areas from analysis. As shown in Figure 1, a variety of spectra was obtained, each resulting from different relative contributions of the Fe-bearing minerals present in the sample. Because the nine samples are reasonably mixtures of the same Fe-bearing phases in variable proportions, the nine spectra were fit simultaneously (simfit) with a common model, adjusting parameters to a single minimum chi-squared convergence criterion [2]. The starting point for the fitting model and values of hyperfine parameters was the work of Solberg and Burns [3], who identified olivine, pyroxene, and ferrous glass as major, and ilmenite and a ferric phase as minor (<5%), Fe-bearing phases in EET79001.
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mineralogy composition and alteration of mars pathfinder rocks and soils evidence from multispectral elemental and magnetic data on terrestrial analogue SNC Meteorite and pathfinder samples
Journal of Geophysical Research, 2000Co-Authors: Richard V Morris, D C Golden, J F Bell, T D Shelfer, Andreas C Scheinost, Nancy W Hinman, George Furniss, Stanley A Mertzman, J L Bishop, Douglas W MingAbstract:Major element, multispectral, and magnetic properties data were obtained at Ares Vallis during the Mars Pathfinder mission. To understand the compositional, mineralogical, and process implications of these data, we obtained major element, mineralogical, and magnetic data for well-crystalline and nanophase ferric minerals, terrestrial analogue samples with known geologic context, and SNC Meteorites. Analogue samples include unaltered, palagonitic, and sulfatetic tephra from Mauna Kea Volcano (hydrolytic and acid-sulfate alteration), steam vent material from Kilauea Volcano (hydrolytic alteration), and impactites from Meteor Crater (relithification). Salient results for Mars Pathfinder include: (1) Band depths BD530b and BD600 and the reflectivity ratio R800/R750 are consistent with the dominant ferric mineral being nanophase ferric oxide associated with an unknown amount of H2O and occurring in composite particles along with subordinate amounts of other ferric minerals. Hematite and hematite plus nanophase goethite are most consistent with the data, but maghemite, akaganeite, schwertmannite, and nanophase lepidocrocite are also possible interpretations. Ferric oxides that are consistently not favored by the data as sole alteration products are jarosites and well-crystalline goethite and lepidocrocite. (2) The strength of the ferric adsorption edge (R750/R445) implies the Fe3+/Fe2+ values for Pathfinder rock and soil are within the ranges 0.7–3 and 3–20, respectively. (3) Ferrous silicates are indicated for subsets of Pathfinder rocks and soils. One subset has a band minimum near 930 nm that can attributed to low-Ca pyroxene. Alternatively, the band could be a second manifestation of certain ferric oxides, including nanophase goethite, maghemite, akaganeite, and schwertmannite. Another subset has a negative spectral slope from ∼800 to 1005 nm which could result from the high-energy wing of a high-Ca pyroxene and/or olivine band, a mixture of bright and dark materials, and, for rocks, thin coatings of bright dust on dark rocks. (4) Chemical data on Pathfinder rocks and soils are consistent with two-component mixtures between an “andesitic” rock with low MgO and SO3 concentrations (soil-free rock) and a global, basaltic soil with high MgO and SO3 concentrations (rock-free soil). Pathfinder rock-free soil can be modeled as a chemical mixture of SNC Meteorites and the Pathfinder soil-free rock. (5) Pathfinder soil cannot be obtained by chemical alteration of Pathfinder rocks by any of the hydrolytic and acid-sulfate alteration processes we studied. Presumably, global mixing has obscured and possibly erased the elemental signatures of chemical alteration. (6) The strongly magnetic phase in palagonitic and sulfatetic tephra is titanomagnetite and possibly its oxidation product titanomaghemite (Fe-Ti spinels). The saturation magnetization of the tephra samples (0.5–2.0 Am2/kg) is at or below the low end of the range inferred for Martian dust (4±2 Am2/kg), implying that lithogenic Fe-Ti spinels are a possible candidate for the Martian strongly magnetic phase. (7) The predominantly palagonitic spectral signature and magnetic nature of Martian soil and dust are consistent with glassy precursors with imbedded Fe-Ti spinel particles. Comparison with lunar glass production rates suggests that production of sufficient quantities of glassy materials on Mars by volcanic and impact processes is sufficient to account for these observations.
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mineralogic and compositional properties of martian soil and dust results from mars pathfinder
Journal of Geophysical Research, 2000Co-Authors: J F Bell, Richard V Morris, H Y Mcsween, J A Crisp, S L Murchie, N T Bridges, J R Johnson, D T Britt, M P Golombek, H J MooreAbstract:Mars Pathfinder obtained multispectral, elemental, magnetic, and physical measurements of soil and dust at the Sagan Memorial Station during the course of its 83 sol mission. We describe initial results from these measurements, concentrating on multispectral and elemental data, and use these data, along with previous Viking, SNC Meteorite, and telescopic results, to help constrain the origin and evolution of Martian soil and dust. We find that soils and dust can be divided into at least eight distinct spectral units, based on parameterization of Imager for Mars Pathfinder (IMP) 400 to 1000 nm multispectral images. The most distinctive spectral parameters for soils and dust are the reflectivity in the red, the red/blue reflectivity ratio, the near-IR spectral slope, and the strength of the 800 to 1000 nm absorption feature. Most of the Pathfinder spectra are consistent with the presence of poorly crystalline or nanophase ferric oxide(s), sometimes mixed with small but varying degrees of well-crystalline ferric and ferrous phases. Darker soil units appear to be coarser-grained, compacted, and/or mixed with a larger amount of dark ferrous materials relative to bright soils. Nanophase goethite, akaganeite, schwertmannite, and maghemite are leading candidates for the origin of the absorption centered near 900 nm in IMP spectra. The ferrous component in the soil cannot be well-constrained based on IMP data. Alpha proton X-ray spectrometer (APXS) measurements of six soil units show little variability within the landing site and show remarkable overall similarity to the average Viking-derived soil elemental composition. Differences exist between Viking and Pathfinder soils, however, including significantly higher S and Cl abundances and lower Si abundances in Viking soils and the lack of a correlation between Ti and Fe in Pathfinder soils. No significant linear correlations were observed between IMP spectral properties and APXS elemental chemistry. Attempts at constraining the mineralogy of soils and dust using normative calculations involving mixtures of smectites and silicate and oxide minerals did not yield physically acceptable solutions. We attempted to use the Pathfinder results to constrain a number of putative soil and dust formation scenarios, including palagonitization and acid-fog weathering. While the Pathfinder soils cannot be chemically linked to the Pathfinder rocks by palagonitization, this study and McSween et al. [1999] suggest that palagonitic alteration of a Martian basaltic rock, plus mixture with a minor component of locally derived andesitic rock fragments, could be consistent with the observed soil APXS and IMP properties.
A H Treiman - One of the best experts on this subject based on the ideXlab platform.
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the nakhla martian Meteorite is a cumulate igneous rock comment on glass bearing inclusions in nakhla SNC Meteorite augite heterogeneously trapped phases 2001 by m e varela g kurat and r clocchiatti
Mineralogy and Petrology, 2003Co-Authors: A H TreimanAbstract:¶All the properties of the Nakhla Martian Meteorite suggest that it is a cumulate igneous rock, formed from a basaltic parental magma. Anomalous magmatic inclusions in Nakhla’s augite grains (Varela et al., 2001) can be explained by disequilibrium processes during crystal growth, and have little significance in the geological history of the Meteorite.
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The Nakhla Martian Meteorite is a Cumulate Igenous Rock. Comment on "Glass-Bearing Inclusions in Nakhla (SNC Meteorite) Augite: Heterogeneously Trapped Phases"
2003Co-Authors: A H TreimanAbstract:All the properties of the Nakhla Martian Meteorite suggest that it is a cumulate igneous rock, formed from a basaltic parental magma. Anomalous magmatic inclusions in Nakhla s augite grains can be explained by disequilibrium processes during crystal growth, and have little significance in the geological history of the Meteorite.
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the parent magma of the nakhla SNC Meteorite reconciliation of composition estimates from magmatic inclusions and element partitioning
Lunar and Planetary Science Conference, 1993Co-Authors: A H TreimanAbstract:The composition of the parent magma of the Nakhla Meteorite was difficult to determine, because it is accumulate rock, enriched in olivine and augite relative to a basalt magma. A parent magma composition is estimated from electron microprobe area analyses of magmatic inclusions in olivine. This composition is consistent with an independent estimate based on the same inclusions, and with chemical equilibria with the cores of Nakhla's augites. This composition reconciles most of the previous estimates of Nakhla's magma composition, and obviates the need for complex magmatic processes. Inconsistency between this composition and those calculated previously suggests that magma flowed through and crystallized into Nakhla as it cooled.