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1.
The Northwest Africa (NWA) 7475 meteorite is one of the several stones of paired regolith breccias from Mars based on petrography, oxygen isotope, mineral compositions, and bulk rock compositions. Its inventory of lithic clasts is dominated by vitrophyre impact melts that were emplaced while they were still molten. Other clast types include crystallized impact melt rocks, evolved plutonic rocks, possible basalts, contact metamorphosed rocks, and siltstones. Impact spherules and vitrophyre shards record airborne transport, and accreted dust rims were sintered on most clasts, presumably during residence in an ejecta plume. The clast assemblage records at least three impact events, one that formed an impact melt sheet on Mars ≤4.4 Ga ago, a second that assembled NWA 7475 from impactites associated with the impact melt sheet at 1.7–1.4 Ga, and a third that launched NWA 7475 from Mars ~5 Ma ago. Mildly shocked pyroxene and plagioclase constrain shock metamorphic conditions during launch to >5 and <15 GPa. The mild postshock‐heating that resulted from these shock pressures would have been insufficient to sterilize this water‐bearing lithology during launch. Magnetite, maghemite, and pyrite are likely products of secondary alteration on Mars. Textural relationships suggest that calcium‐carbonate and goethite are probably of terrestrial origin, yet trace element chemistry indicates relatively low terrestrial alteration. Comparison of Mars Odyssey gamma‐ray spectrometer data with the Fe and Th abundances of NWA 7475 points to a provenance in the ancient southern highlands of Mars. Gratteri crater, with an age of ~5 Ma and an apparent diameter of 6.9 km, marks one possible launch site of NWA 7475.  相似文献   

2.
Abstract– Northwest Africa (NWA) 5298 is an evolved basaltic shergottite that has bulk characteristics and mineral compositions consistent with derivation from an oxidized reservoir in Mars. Chemically zoned clinopyroxene (64.5%, augite and pigeonite), with interstitial lath‐shaped plagioclase (29.4%, An40 to An55), constitutes the bulk of this meteorite. The plagioclase has been converted by shock to both isotropic maskelynite and spherulitic, birefringent feldspar representing a quenched vesicular melt. The remainder of the rock consists of minor amounts of Fe‐Ti oxides (ilmenite and titanomagnetite), phosphates (merrillite and apatite), silica polymorph, fayalite, pyrrhotite, baddeleyite, and minor hot desert weathering products (calcite and barite). Oxygen fugacity derived from Fe‐Ti oxide thermobarometry is close to the quartz‐fayalite‐magnetite (QFM) buffer indicating that the late stage evolution of this magma occurred under more oxidizing condition than those recorded in most other shergottites. Merrillite contains the largest abundances of rare earth elements (REE) of all phases, thereby controlling the REE budget in NWA 5298. The calculated bulk rock REE pattern normalized to CI chondrite is relatively flat. The evolution of the normalized REE patterns of the bulk rock, clinopyroxene, plagioclase, and phosphate in NWA 5298 is consistent with closed‐system chemical behavior with no evidence of crustal contamination or postcrystallization disturbance of the REE contents of these phases.  相似文献   

3.
Abstract— Magmatic sulfide mineralogy has been studied in 2 olivine‐phyric shergottites (DaG 476 and SaU 005) and 4 basaltic shergottites (Zagami, Shergotty, Los Angeles, and NWA 480). Modal abundances of magmatic sulfides, as estimated by image analysis on thin section, are high (0.16 to 0.53 area percent) and correlate positively with abundances of Fe‐Ti oxides. Sulfides are mesostasis minerals, being mostly interstitial grains or locally enclosed in post‐cumulus melt inclusions (e.g., SaU 005) in olivine. Sulfides in shergottites are composed of major pyrrhotite containing pentlandite exsolutions associated with minor amounts of Cu sulfides (chalcopyrite and/or cubanite). Hot desert finds (e.g., DaG 476) show abundant fracture‐filling iron (oxy)hydroxides of probable terrestrial origin. Unaltered sulfides show metal‐rich hexagonal pyrrhotite compositions with metal/sulfur (M/S) ratio ranging between 0.936 ± 0.005 and 0.962 ± 0.01. This compositional range corresponds to the two‐phase structural domain 2C + nC of the Fe‐S system; however, the high‐temperature disordered hexagonal 1C pyrrhotite structure would be in better agreement with magnetic properties of shergottites. Ni contents in pyrrhotite increase from Los Angeles (<0.05 at%) to Shergotty, Zagami, and NWA 480 (0.2–0.5 at%), and DaG 476 and SaU 005 (up to 3 at%). The higher Ni values of pyrrhotite in olivine‐phyric shergottites correlate with the abundance of pentlandite exsolutions, both reflecting more primitive Ni‐rich sulfide liquids where abundant olivine crystallized. This result and the strong correlation between sulfide abundances and Fe‐Ti oxides argue for a primary magmatic origin of these sulfides. Although they reproduce the trend of magmatic oxygen fugacity conditions determined from Fe‐Ti oxide pairs, observed pyrrhotite compositions are systematically more metal‐deficient compared to those calculated from the Fe‐S‐O system. This suggests post‐magmatic oxidation during cooling on Mars, followed by terrestrial weathering for hot desert finds.  相似文献   

4.
During its three flybys of Mercury, the MESSENGER spacecraft made the first detection of gamma-ray emission from the planet's surface. With a closest approach distance of ∼200 km, the flybys provided an opportunity to measure elemental abundances of Mercury's near-equatorial regions, which will not be visited at low altitude during MESSENGER's orbital mission phase. Despite being limited by low planetary photon flux, sufficient counts were accumulated during the first two flybys to estimate bounds on abundances for some elements having relatively strong gamma-ray spectral peaks, including Si, Fe, Ti, K, and Th. Only for Si is the standard deviation σ sufficiently small to conclude that this element was detected with 99% confidence. Iron and potassium are detected at the 2−σ (95% confidence) level, whereas only upper bounds on Ti and Th can be determined. Relative to a Si abundance assumed to be 18 weight percent (wt%), 2−σ upper bounds have been estimated as 9.7 wt% for Fe, 7.0 wt% for Ti, 0.087 wt% for K, and 2.2 ppm for Th. The relatively low upper bound on K rules out some previously suggested models for surface composition for the regions sampled. Upper bounds on Fe/Si and Ti/Si ratios are generally consistent with Ti and Fe abundances estimated from the analysis of measurements by the MESSENGER Neutron Spectrometer during the flybys but are also permissive of much lower concentrations.  相似文献   

5.
The chemical compositions of shergottite meteorites, basaltic rocks from Mars, provide a broad view of the origins and differentiation of these Martian magmas. The shergottite basalts are subdivided based on their Al contents: high‐Al basalts (Al > 5% wt) are distinct from low‐Al basalts and olivine‐phyric basalts (both with Al < 4.5% wt). Abundance ratios of highly incompatible elements (e.g., Th, La) are comparable in all the shergottites. Abundances of less incompatible elements (e.g., Ti, Lu, Hf) in olivine‐phyric and low‐Al basalts correlate well with each other, but the element abundance ratios are not constant; this suggests mixing between components, both depleted and enriched. High‐Al shergottites deviate from these trends consistent with silicate mineral fractionation. The “depleted” component is similar to the Yamato‐980459 magma; approximately, 67% crystal fractionation of this magma would yield a melt with trace element abundances like QUE 94201. The “enriched” component is like the parent magma for NWA 1068; approximately, 30% crystal fractionation from it would yield a melt with trace element abundances like the Los Angeles shergottite. This component mixing is consistent with radiogenic isotope and oxygen fugacity data. These mixing relations are consistent with the compositions of many of the Gusev crater basalts analyzed on Mars by the Spirit rover (although with only a few elements to compare). Other Mars basalts fall off the mixing relations (e.g., Wishstone at Gusev, Gale crater rocks). Their compositions imply that basalt source areas in Mars include significant complexities that are not present in the source areas for the shergottite basalts.  相似文献   

6.
Alberto G. Fairén 《Icarus》2010,208(1):165-48
Water on Mars has been explained by invoking controversial and mutually exclusive solutions based on warming the atmosphere with greenhouse gases (the “warm and wet” Mars) or on local thermal energy sources acting in a global freezing climate (the “cold and dry” Mars). Both have critical limitations and none has been definitively accepted as a compelling explanation for the presence of liquid water on Mars. Here is considered the hypothesis that cold, saline and acidic liquid solutions have been stable on the sub-zero surface of Mars for relatively extended periods of time, completing a hydrogeological cycle in a water-enriched but cold planet. Computer simulations have been developed to analyze the evaporation processes of a hypothetical martian fluid with a composition resulting from the acid weathering of basalt. This model is based on orbiter- and lander-observed surface mineralogy of Mars, and is consistent with the sequence and time of deposition of the different mineralogical units. The hydrological cycle would have been active only in periods of dense atmosphere, as having a minimum atmospheric pressure is essential for water to flow, and relatively high temperatures (over ∼245 K) are required to trigger evaporation and snowfall; minor episodes of limited liquid water on the surface could have occurred at lower temperatures (over ∼225 K). During times with a thin atmosphere and even lesser temperatures (under ∼225 K), only transient liquid water can potentially exist on most of the martian surface. Assuming that surface temperatures have always been maintained below 273 K, Mars can be considered a “cold and wet” planet for a substantial part of its geological history.  相似文献   

7.
Abstract— Bulk chemical compositions of the shergottite basalts provide important constraints on magma genesis and mantle processes in Mars. Abundances of many major and trace elements in the shergottites covary in 2 distinct groups: Group 1 (Gl) includes mostly highly incompatible elements (e.g., La, Th), and Group 2 (G2) includes mostly moderately incompatible elements (e.g., Ti, Lu, Al, Hf). Covariations of G2 elements (not necessarily linear) are consistent with partitioning between basalt magma and orthopyroxene + olivine. This fractionation represents partial melting to form the shergottites and their crystallization; the restite minerals cannot include aluminous phase(s), phosphate, ilmenite, zircon, or sulfides. Overall, abundances of Gl elements are decoupled from those of G2. In graphing abundances of a Gl element against those of a G2 element, G1/G2 abundance ratios do not appear to be random but are restricted to 4 values. Shergottites with a given G1/G2 value need not have the same crystallization age and need not fall on a single fractionation trajectory involving compatible elements (e.g., Ti versus Fe*). These observations imply that the G1/G2 families were established before basalt formation and suggest metasomatic enrichment of their source region (major carrier of G2 elements) by a component rich in Gl elements. Group 1 elements were efficiently separated from G2 elements very early in Mars' history. Such efficient fractionation is not consistent with simple petrogenesis; it requires multiple fractionations, “complex” petrogenetic processes, or minerals with unusual geochemistry. The behavior of phosphorus in this early fractionation event is inexplicable by normal petrogenetic processes and minerals. Several explanations are possible, including significant compatibility of P in majoritic garnet and the presence of P‐bearing iron metal (or a phosphide phase) in the residual solid assemblage (carrier of G2 elements). If the latter, Mars' mantle is more oxidized now than during the ancient fractionation event.  相似文献   

8.
James L. Gooding 《Icarus》1978,33(3):483-513
Chemical weathering on Mars is examined theoretically from the standpoint of heterogeneous equilibrium between solid mineral phases and gaseous O2, H2O, and CO2 in the Martian atmosphere. Thermochemical calculations are performed in order to identify important gas-solid decomposition reactions involving the major mineral constituents of mafic igneous rocks. Where unavailable in the thermochemical literature, Gibbs free energy and enthalpy of formation are estimated for certain minerals and details of these estimation procedures are given. Partial pressure stability diagrams are presented to show pertinent mineral reaction boundaries at 298 and at 240°K. In the present Martian environment, the thermodynamically stable products of gas-solid weathering of individual minerals at 240°K should be Fe2O3, as hematite or maghemite (from fayalite, magnetite, and Fe-bearing pyroxenes), quartz (from all silicates), calcite (from Ca-bearing pyroxenes and plagioclase), magnesite (from forsterite and Mg-bearing pyroxenes), corundum (from all Al-bearing silicates), Ca-beidellite (from anorthite), and szomolnokite, FeSO4 or FeSO4·H2O (from iron sulfides). Albite, microcline, and apatite should be stable with respect to gas-solid decomposition, suggesting that gas-solid weathering products on Mars may be depleted in Na, K, and P (and, possibly, Cl and F). Certain montmorillonite-type clay minerals are thermodynamically favorable intermediate gas-solid decomposition products of Al-bearing pyroxenes and may be metastable intermediate products of special mineral surface reaction mechanisms. However, the predicted high thermodynamic susceptibility of these clay minerals to subsequent gas-solid decomposition implies that they should ultimately decompose in the present Martian surface environment. Kaolinite is apparently the only clay mineral which should be thermodynamically stable over all ranges of temperature and water vapor abundance in the present environment at the Martian surface. Considering thermodynamic criteria, including possible gas-solid decomposition reactions, it is doubtful that significant amounts of goethite and clay minerals can be currently forming on Mars by mechanisms known to operate to Earth. If major amounts of goethite and clay minerals occur on Mars, they probably owe their existence to formation in an environment characterized by the presence of liquid water or by mechanism possibly unique to Mars. In any case, any goethite or montmorillonite-type clay mineral on Mars must ultimately decompose.  相似文献   

9.
Chemical equilibrium calculations on the stability of pure and dissolved graphite and cohenite (Fe3C), several other carbides, and several carbonates have been carried out for a system with solar elemental abundances over a very wide range of temperature and pressure. The calculated abundances of condensed carbon compounds are similar to the observed inventories on Earth and Venus, but fully 10 times smaller than the minimum carbon abundance found in ordinary chondrites. The total carbon content of most iron meteorites is compatible with their origin as a cooling FeNiCSP solution which was saturated with dissolved carbon at the solidus, such as would be produced by melting an ordinary chondrite, not by direct condensation from or equilibrium with the primitive solar nebula. It is argued that the carbon content of Mars need not be appreciably greater than that of the Earth. Material with even lower formation temperatures than Mars, such as the primitive material in the asteroid belt, may retain substantially more carbon as disequilibrium polymeric organic matter, possibly by the Fischer-Tropsch mechanism favored by Anders. Carbonates are not found as equilibrium products in a solar-composition system, and are probably secondary alteration products. CaCO3 might, however, persist in a solar-composition gas at temperatures below 460°K and pressures below 10?6.6 bar. The most stable condensed carbon compounds are found to be graphite, Fe3C, and possibly TiC, all in solid solution in the metal phase.  相似文献   

10.
The element Fe and Fe-bearing minerals occur ubiquitously throughout the field of astrobiology. Cycling between the various oxidation states of Fe provides a source of energy available for life. Banded iron formations may record the rise of oxygenic photosynthesis. The distribution of Fe between Fe-bearing minerals and its oxidation states can help to characterize and understand ancient environments with respect to the suitability for life by constraining the primary rock type and the redox conditions under which it crystallized, the extent of alteration and weathering, the type of alteration and weathering products, and the processes and environmental conditions for alteration and weathering. Fe Mössbauer spectroscopy is a powerful tool to investigate Fe-bearing compounds. It can identify Fe-bearing minerals, determine Fe oxidation states with high accuracy, quantify the distribution of Fe between mineralogical phases, and provide clues about crystallinity and particle sizes. Two miniaturized Mössbauer spectrometers are on board of the NASA Mars Exploration Rovers Spirit and Opportunity. The Fe-bearing minerals goethite, an iron oxide-hydroxide, and jarosite, an iron hydroxide sulfate, were identified by Mössbauer spectroscopy in Gusev Crater and at Meridiani Planum, respectively, providing in situ proof of an aqueous history of the two landing sites and constraints on their habitability. Hematite identified by Mössbauer spectroscopy at both landing sites adds further evidence for an aqueous history. On Earth, Mössbauer spectroscopy was used to monitor possibly microbially-induced changes of Fe-oxidation states in basaltic glass samples exposed at the Loihi Seamount, a deep sea hydrothermal vent system, which might be analogous to possible extraterrestrial habitats on ancient Mars or the Jovian moon Europa today.  相似文献   

11.
Abstract– The Dawn spacecraft carries a gamma‐ray and neutron detector (GRaND), which will measure and map the abundances of selected elements on the surface of asteroid 4 Vesta. We compare the variability of moderately volatile/refractory incompatible element ratios (K/Th and K/Ti) in howardite, eucrite, and diogenite (HED) meteorites with those in other achondrite suites that represent asteroidal crusts, because these ratios may be accurately measured by GRaND and likely reflect initial chemical compositions of the HED parent body. The K/Th and K/Ti variations can differentiate HED meteorites from angrites and some unique eucrite‐like lithologies. The results suggest that K, Th, and Ti abundances determined from GRaND data could not only confirm that Vesta is the parent body of HED meteorites but might also allow recognition of as‐yet unsampled compositional terranes on Vesta. Besides the K‐Th‐Ti systematics study, we propose a new three‐component mixing model for interpretation of GRaND spectra, required because the spatial resolution of GRaND is coarser than the spectral (compositional) heterogeneity of Vesta’s surface. The mixing model uses abundances of K, Ti, Fe, and Mg that will be analyzed more accurately than other prospective GRaND‐analyzed elements. We examine propagated errors due to GRaND analytical uncertainties and intrinsic errors that stem from an assumption introduced into the mixing model. The error investigation suggests that the mixing model can adequately estimate not only the diogenite/eucrite mixing ratio but also the abundances of most major and minor elements within the GRaND propagated errors.  相似文献   

12.
Dynamical transport of gases within the martian regolith controls many climatic processes, and is particularly important in the deposition and/or mobilization of shallow ground ice, as well as exchange of other volatiles between the martian regolith and atmosphere. A variety of theoretical studies have addressed issues related to ground ice dynamics on Mars and in the terrestrial analog environment of the Antarctic Dry Valleys. These theoretical studies have drawn on a limited set of empirical measurements to constrain the structural parameters controlling gas diffusion and flow in soils. Here, we investigate five groups of Mars-analog soils: glass spheres, JSC Mars-1, aeolian dune sand, Antarctic Dry Valley soils, and arctic loess. We present laboratory measurements of the structural properties most relevant to gas transport in these soils: porosity, tortuosity, permeability, bulk and intrinsic densities, grain-size distribution, pore-size distribution and BET surface area. Our results bear directly both on the appropriateness of assumptions made in theoretical studies and on current outstanding issues in the study of shallow ground ice on Mars and in the Dry Valleys. Specifically, we find that (1) measured values of tortuosity are lower than values commonly assumed for Mars by a factor of two to three; (2) diffusive loss of ground ice on Mars can likely proceed up to four times faster than predicted by theoretical studies; (3) soil permeabilities are sufficiently high that flushing of the soil column by bulk flow of atmospheric gases may further speed loss or deposition of shallow ground ice; (4) the pore volume in some Mars-analog soils is sufficiently high to explain high volumetric ice abundances inferred from Mars Odyssey Gamma Ray Spectrometer data as simple pore ice; and (5) measured properties of soils collected in Beacon Valley, Antarctica agree well with assumptions made in theoretical studies and are consistent with rapid loss of ground ice in the current climate.  相似文献   

13.
Abstract— Roosevelt County (RC) 075 was recovered in 1990 as a single 258-gram stone. Classification of this meteorite is complicated by its highly unequilibrated nature and its severe terrestrial weathering, but we favor H classification. This is supported by O isotopes and estimates of the original Fe, Ni metal content. The O isotopic composition is similar to that of a number of reduced ordinary chondrites (e.g., Cerro los Calvos, Willaroy), although RC 075 exhibits no evidence of reduced mineral compositions. Chondrule diameters are consistent with classification as an L chondrite, but large uncertainties in chondrule diameters of RC 075 and poorly constrained means of H, L and LL chondrites prevent use of this parameter for reliable classification. Other parameters are compromised by severe weathering (e.g., siderophile element abundances) or unsuitable for discrimination between unequilibrated H, L and LL chondrites (e.g., Co in kamacite, δ13C). Petrologic subtype 3.2± 0.1 is suggested by the degree of olivine heterogeneity, the compositions of chondrule olivines, the thermoluminescence sensitivity, the abundances and types of chondrules mapped on cathodoluminescence mosaics, and the amount of presolar SiC. The meteorite is very weakly shocked (S2), with some chondrules essentially unshocked and, thus, is classified as an H3.2(S2) chondrite. Weathering is evident by a LREE enrichment due to clay contamination, reduced levels of many siderophile elements, the almost total loss of Fe, Ni metal and troilite, and the reduced concentrations of noble gases. Some components of the meteorite (e.g., type IA chondrules, SiC) appear to preserve their nebular states, with little modification from thermal metamorphism. We conclude that RC 075 is the most unequilibrated H chondrite yet recovered and may provide additional insights into the origin of primitive materials in the solar nebula.  相似文献   

14.
108 +/- 11 photons of the martian He 584-angstroms airglow detected by the Extreme Ultraviolet Explorer satellite during a 2-day exposure (January 22-23, 1993) correspond to the effective disk average intensity of 43 +/- 10 Rayleigh. Radiative transfer calculations, using a model atmosphere appropriate to the conditions of the observation and having an exospheric temperature of 210 +/- 20 K, result in a He mixing ratio of 1.1 +/- 0.4 ppm in the lower atmosphere. Nonthermal escape of helium is due to electron impact ionization and pickup of He+ by the solar wind, to collisions with hot oxygen atoms, and to charge exchange with molecular species with corresponding column loss rates of 1.4 x 10(5), 3 x 10(4), and 7 x 10(3) cm-2 sec-1, respectively. The lifetime of helium on Mars is 5 x 10(4) years. The He outgassing rate, coupled with the 40Ar atmospheric abundance and with the K:U:Th ratio measured in the surface rocks, is used as input to a single two-reservoir degassing model which is applied to Mars and then to Venus. A similar model with known abundances of K, U, and Th is applied to Earth. The models for Earth and Mars presume loss of all argon accumulated in the atmospheres during the first billion years by large-scale meteorite and planetesimal impacts. The models show that the degassing coefficients for all three planets may be approximated by function delta = delta (0)(t(0)/t)1/2 with delta (0) = 0/1, 0.04, and 0.0125 Byr-1 for Earth, Venus, and Mars, respectively. After a R2 correction this means that outgassing processes on Venus and Mars are weaker than on Earth by factors of 3 and 30, respectively. Mass ratios of U and Th are almost the same for all three planets, while potassium is depleted by a factor of 2 in Venus and Mars. Mass ratios of helium and argon are close to 5 x 10(-9) and 2 x 10(-8) g/g in the interiors of all three planets. The implications of these results are discussed.  相似文献   

15.
Chevrel  S. D.  Pinet  P. C.  Daydou  Y.  Feldman  W. C. 《Solar System Research》2002,36(6):458-459
In this paper, we present (1) a statistical analysis, based on a systematic clustering method, of a dataset integrating the global abundance maps of the three elements iron, titanium, and thorium derived from Clementine and Lunar Prospector and (2) a comparison of iron abundances between Clementine and Lunar Prospector. Homogeneous geologic units are compositionally characterized and spatially defined in relation to the major rock types sampled on the Moon. With the lowest abundances of Fe, Ti, and Th found on the Moon, the lunar highland terrains are quite homogeneous with two major large feldspathic units, one being slightly more mafic than the other. Two distinct regions with unique compositions are unambiguously identified: the Procellarum KREEP Terrane (PKT) and the South Pole–Aitken (SPA). The PKT, which includes all the units with Th abundances higher than 3.5 ppm (KREEP-rich materials), is delimited by an almost continuous ringlike unit. In particular, it includes the western nearside maria, except for Mare Humorum. With concentrations in Fe, Ti, and Th enhanced relative to the surrounding highlands, the South Pole–Aitken basin floor represents a large mafic anomaly on the far side, suggesting wide deposits of lower crust and possible mantle materials. However, due to indirect residual latitude effects in the CSR (Clementine spectral reflectance) measurements, iron abundances might have been overestimated in SPA, thus implying that crustal materials, rather than mantle materials, might represent the dominant contributor to the mafic component exposed on the basin floor.  相似文献   

16.
Abstract— We compiled a table of all major, minor, and trace-element abundances in 89 interplanetary dust particles (IDPs) that includes data obtained with proton-induced x-ray emission (PIXE), synchroton x-ray fluorescence (SXRF), and secondary ion mass spectrometry (SIMS). For the first time, the reliability of the trace-element abundances in IDPs is tested by various crosschecks. We also report on the results of cluster analyses that we performed on IDP compositions. Because of the incompleteness of the data set, we included only the elements Cr, Mn, Ni, Cu, and Zn, normalized to Fe and CI chondrite abundances, that are determined in 73 IDPs. The data arrange themselves in four rather poorly defined groups that we discuss in relation to CI chondrites following the assumption that on the average CI abundances are most probable. The largest group (chondritic), with 44 members, has close to CI abundances for many refractory and moderately refractory elements (Na, Al, Si, P, K, Sc, Ti, V, Cr, Co, Ge, Sr). It is slightly depleted in Fe and more in Ca and S, while the volatile elements (Cl, Cu, Zn, Ga, Se, Rb) are enriched by =1.7 × CI and Br by 21 × CI. The low-Zn group, with 12 members, is very similar to the chondritic group except for its Zn-depletion, stronger Ca-depletion and Fe-enrichment. The low-Ni group, with 11 members, has Ni/Fe = 0.03 × CI and almost CI-like Ca, but its extraterrestrial origin is not established. The last group (6 members) contains non-systematic particles of unknown origin. We found that Fe is inhomogeneously distributed on a micron scale. Furthermore, the abundances of elements that are measured near their limits of detection are easily overestimated. These biases involved, the incomplete data set and possible contaminating processes prevent us from obtaining information on the specific origin(s) of IDPs from elemental abundances.  相似文献   

17.
Abstract— The trace element compositions and noble gas contents of 32 individual interplanetary dust particles (IDPs) collected in the Earth's stratosphere were measured. Trace element compositions are generally similar to CI meteorites, with occasional depletions in Zn/Fe with respect to CI. Noble gases were detected in all but one of the IDPs. Noble gas elemental compositions are consistent with the presence of fractionated solar wind. A rough correlation between surface‐normalized He abundances and Zn/Fe ratios is observed; Zn‐poor particles generally have lower He contents than the other IDPs. This suggests that both elements were lost by frictional heating during atmospheric entry and confirms the view that Zn can serve as an entry‐heating indicator in IDPs.  相似文献   

18.
A. Gaudin  E. Dehouck  N. Mangold 《Icarus》2011,216(1):257-268
Phyllosilicates on Mars are widespread in the ancient crust suggesting the presence of liquid water at the martian surface and therefore warmer conditions during its early history. However, the role of the ancient climate in the alteration process, which produced these phyllosilicates, remains under debate, because similar mineral assemblages can be produced by hydrothermal alteration at depth. This paper focuses on the origin of coincident outcrops of Fe/Mg bearing phyllosilicates and Al-bearing phyllosilicates, which are observed in several regions of Mars. We performed a detailed mineralogical comparison between a section in Nili Fossae, Mars, and a weathering profile located at Murrin Murrin, Western Australia. The Murrin Murrin profile is developed in Archaean serpentinized peridotite massifs over a ∼40 m thick sequence. It has three alteration zones: the serpentine mineral saprolite is found at the bottom, immediately overlain by Fe/Mg-bearing smectites and then Al-bearing phyllosilicates (kaolinite) mixed with iron hydroxides. This example illustrates how Al-dominated minerals can derive from the alteration of initially Al-poor ultramafic rocks by the intense leaching of Mg2+. This mineralogical sequence is very similar to that detected locally in Nili Fossae by orbital spectroscopy. By analogy, we propose that the mineral assemblage detected on Mars is the result of long-term weathering, and thus could be the best evidence of past weathering as a direct result of a climate significantly warmer than at present.  相似文献   

19.
Abstract— The major element, trace element, and isotopic compositional ranges of the martian basaltic meteorite source regions have been modeled assuming that planetary differentiation resulted from crystallization of a magma ocean. The models are based on low to high pressure phase relationships estimated from experimental runs and estimates of the composition of silicate Mars from the literature. These models attempt to constrain the mechanisms by which the martian meteorites obtained their superchondritic CaO/Al2O3 ratios and their source regions obtained their parent/daughter (87Rb/86Sr, 147Sm/144Nd, and 176Lu/177Hf) ratios calculated from the initial Sr, Nd, and Hf isotopic compositions of the meteorites. High pressure experiments suggest that majoritic garnet is the liquidus phase for Mars relevant compositions at or above 12 GPa. Early crystallization of this phase from a martian magma ocean yields a liquid characterized by an elevated CaO/Al2O3 ratio and a high Mg#. Olivine‐pyroxene‐garnet‐dominated cumulates that crystallize subsequently will also be characterized by superchondritic CaO/Al2O3 ratios. Melting of these cumulates yields liquids with major element compositions that are similar to calculated parental melts of the martian meteorites. Furthermore, crystallization models demonstrate that some of these cumulates have parent/daughter ratios that are similar to those calculated for the most incompatible‐element‐depleted source region (i.e., that of the meteorite Queen Alexandra [QUE] 94201). The incompatible‐element abundances of the most depleted (QUE 94201‐like) source region have also been calculated and provide an estimate of the composition of depleted martian mantle. The incompatible‐element pattern of depleted martian mantle calculated here is very similar to the pattern estimated for depleted Earth's mantle. Melting the depleted martian mantle composition reproduces the abundances of many incompatible elements in the parental melt of QUE 94201 (e.g., Ba, Th, K, P, Hf, Zr, and heavy rare earth elements) fairly well but does not reproduce the abundances of Rb, U, Ta and light rare earth elements. The source regions for meteorites such as Shergotty are successfully modeled as mixtures of depleted martian mantle and a late stage liquid trapped in the magma ocean cumulate pile. Melting of this hybrid source yields liquids with major element abundances and incompatible‐element patterns that are very similar to the Shergotty bulk rock.  相似文献   

20.
We present an analysis comparing observations acquired by the Mars Express Observatoire pour la Minéralogie l’Eau, les Glaces et l’Activité (OMEGA) and Phoenix lander measurements. Analysis of OMEGA data provides evidence for hydrous and ferric phases at the Phoenix landing site and the surrounding regions. The 3 μm hydration band deepens with increasing latitude, along with the appearance and deepening of a 1.9 μm H2O band as latitude increases ∼60° polewards. A water content of 10-11% is derived from the OMEGA data for the optical surface at the Phoenix landing site compared to 1-2% derived for subsurface soil by Phoenix lander measurements. The hydration of these regions is best explained by surface adsorbed water onto soil grains. No evidence for carbonate or perchlorate-bearing phases is evident from OMEGA data, consistent with the relatively small abundances of these phases detected by Phoenix. The identification of spectral features consistent with hydrated phases (possibly zeolites) from OMEGA data covering regions outside the landing site and the ubiquitous ferric absorption edge suggest that chemical weathering may play a role in the arctic soils.  相似文献   

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