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1.
Abstract— Dhofar 019 is a new martian meteorite found in the desert of Oman. In texture, mineralogy, and major and trace element chemistry, this meteorite is classified as a basaltic shergottite. Olivine megacrysts are set within a groundmass composed of finer grained olivine, pyroxene (pigeonite and augite), and maskelynite. Minor phases are chromite‐ulvöspinel, ilmenite, silica, K‐rich feldspar, merrillite, chlorapatite, and pyrrhotite. Secondary phases of terrestrial origin include calcite, gypsum, celestite, Fe hydroxides, and smectite. Dhofar 019 is most similar to the Elephant Moraine (EETA) 79001 lithology A and Dar al Gani (DaG) 476/489 shergottites. The main features that distinguish Dhofar 019 from other shergottites are lack of orthopyroxene; lower Ni contents of olivine; the heaviest oxygen‐isotopic bulk composition; and larger compositional ranges for olivine, maskelynite, and spinel, as well as a wide range for pyroxenes. The large compositional ranges of the minerals are indicative of relatively rapid crystallization. Modeling of olivine chemical zonations yield minimum cooling rates of 0.5‐0.8 °C/h. Spinel chemistry suggests that crystallization took place under one of the most reduced conditions for martian meteorites, at an fO2 3 log units below the quartz‐fayalite‐magnetite (QFM) buffer. The olivine megacrysts are heterogeneously distributed in the rock. Crystal size distribution analysis suggests that they constitute a population formed under steady‐state conditions of nucleation and growth, although a few grains may be cumulates. The parent melt is thought to have been derived from partial melting of a light rare earth element‐ and platinum group element‐depleted mantle source. Shergottites, EETA79001 lithology A, DaG 476/489, and Dhofar 019, although of different ages, comprise a particular type of martian rocks. Such rocks could have formed from chemically similar source(s) and parent melt(s), with their bulk compositions affected by olivine accumulation.  相似文献   

2.
Abstract— Antarctic meteorite QUE 94201 is a new basaltic shergottite that is mainly composed of subequal amounts of maskelynite and pyroxenes (pigeonite and augite) plus abundant merrillite and accessory phases. It also contains impact melt. Complex zoning patterns in QUE 94201 pyroxenes revealed by elemental map analyses using an electron microprobe suggest a crystallization sequence from Mg-rich pigeonite (En62Fss30Wog) to extremely Fe-rich pigeonite (En5Fs81Wo14) via {110} Mg-rich augite bands (En44Fs20Wo36) in a single crystal. These textures, along with the abundant plagioclase (maskelynite), indicates single-stage rapid cooling (>5 °C/year) of this rock from a supercooled magma. Transition from Mg-rich augite to Fe-rich pigeonite reflects the onset of plagioclase crystallization. Enrichment of late-stage phases in QUE 94201 implies crystallization from an evolved magma and suggests a different parent magma composition from the other basaltic shergottites. Lithology B of EETA79001 basaltic shergottite contains pyroxenes that show complex zoning with augite bands similar to those in QUE 94201 pyroxene, which suggests similar one-stage rapid cooling. Lithology B of EETA79001 also resembles QUE 94201 in its coarse-grained texture of silicates and its high abundance of maskelynite, although QUE 94201 probably crystallized from a more fractionated magma. We also note that some Apollo lunar mare basalts (e.g., 12020 and 12021) have similar mineralogy and petrology to QUE 94201, especially in pyroxene zoning. All these basaltic rocks with complex pyroxene zoning suggest rapid metastable crystallization from supercooled magmas.  相似文献   

3.
Abstract By mineral and bulk compositions, the Lewis Cliff (LEW) 88516 meteorite is quite similar to the ALHA77005 martian meteorite. These two meteorites are not paired because their mineral compositions are distinct, they were found 500 km apart in ice fields with different sources for meteorites, and their terrestrial residence ages are different. Minerals in LEW88516 include: olivine, pyroxenes (low- and high-Ca), and maskelynite (after plagioclase); and the minor minerals chromite, whitlockite, ilmenite, and pyrrhotite. Mineral grains in LEW88516 range up to a few mm. Texturally, the meteorite is complex, with regions of olivine and chromite poikilitically enclosed in pyroxene, regions of interstitial basaltic texture, and glass-rich (shock) veinlets. Olivine compositions range from Fo64 to Fo70, (avg. Fo67), more ferroan and with more variation than in ALHA77005 (Fo69 to Fo73). Pyroxene compositions fall between En77Wo4 and En65Wo15 and in clusters near En63Wo9 and En53Wo33, on average more magnesian and with more variation than in ALHA77005. Shock features in LEW88516 range from weak deformation through complete melting. Bulk chemical analyses by modal recombination of electron microprobe analyses, instrumental neutron activation, and radiochemical neutron activation confirm that LEW88516 is more closely related to ALHA77005 than to other known martian meteorites. Key element abundance ratios are typical of martian meteorites, as is its non-chondritic rare earth pattern. Differences between the chemical compositions of LEW88516 and ALHA77005 are consistent with slight differences in the proportions of their constituent minerals and not from fundamental petrogenetic differences. Noble gas abundances in LEW88516, like those in ALHA77005, show modest excesses of 40Ar and 129Xe from trapped (shock-implanted) gas. As with other ALHA77005 and the shergottite martian meteorites (except EETA79001), noble gas isotope abundances in LEW88516 are consistent with exposure to cosmic rays for 2.5–3 Ma. The absence of substantial effects of shielding from cosmic rays suggest LEW88516 spent this time as an object no larger than a few cm in diameter.  相似文献   

4.
The fall and recovery of the Tissint meteorite in 2011 created a rare opportunity to examine a Martian sample with a known, short residence time on Earth. Tissint is an olivine‐phyric shergottite that accumulated olivine antecrysts within a single magmatic system. Coarse olivine grains with nearly homogeneous cores of Mg# >80 suggest slow re‐equilibration. Many macroscopic features of this sample resemble those of LAR 06319, including the olivine crystal size distribution and the presence of evolved oxide and olivine compositions. Unlike LAR 06319, however, no magmatic hydrous phases were found in the analyzed samples of Tissint. Minor and trace element compositions indicate that the meteorite is the product of closed‐system crystallization from a parent melt derived from a depleted source, with no obvious addition of a LREE‐rich (crustal?) component prior to or during crystallization. The whole‐rock REE pattern is similar to that of intermediate olivine‐phyric shergottite EETA 79001 lithology A, and could also be approximated by a more olivine‐rich version of depleted basaltic shergottite QUE 94201. Magmatic oxygen fugacities are at the low end of the shergottite range, with log fO2 of QFM‐3.5 to ‐4.0 estimated based on early‐crystallized minerals and QFM‐2.4 estimated based on the Eu in pyroxene oxybarometer. These values are similarly comparable to other depleted shergottites, including SaU 005 and QUE 94201. Tissint occupies a previously unsampled niche in shergottite chemistry: containing olivines with Mg# >80, resembling the enriched olivine‐phyric shergottite LAR 06319 in its crystallization path, and comparable to intermediate olivine‐phyric shergottite EETA 79001A, depleted olivine‐phyric shergottite DaG 476, and depleted basaltic shergottite QUE 94201 in its trace element abundances and oxygen fugacity. The apparent absence of evidence for terrestrial alteration in Tissint (particularly in trace element abundances in the whole‐rock and individual minerals) confirms that exposure to the arid desert environment results in only minimal weathering of samples, provided the exposure times are brief.  相似文献   

5.
Abstract— Cosmic-ray produced nuclear tracks and noble gases have been studied in the martian orthopyroxenite Allan Hills 84001 to delineate its cosmic-ray exposure history, preatmospheric size, and fall characteristics. A K-Ar age of 3.9 Ga, cosmic-ray exposure duration of 16.7 Ma, and a preatmospheric radius of 10 cm have been deduced from the noble gas and track data. The track data suggest ALH 84001 to be a single fall that has suffered atmospheric mass ablation in excess of 85%, higher than the value deduced for the shergottites, ALHA 77005, EETA 79001, and Shergotty. The formation age, as well as the cosmic-ray exposure duration, determined in this work are in good agreement with values reported earlier and are distinctly different from other shergottite, nakhlite, and chassignite (SNC) meteorites analysed so far. The high cosmogenic 22Ne/21Ne ratio of 1.22 most probably reflects an effect due to non-chondritic composition of ALH 84001 as the track data suggest high shielding (<5cm) for the analysed samples. There are signatures in the noble gas data that indicate the possible presence of trapped Ar and Ne of martian atmospheric origin in ALH 84001.  相似文献   

6.
Abstract— Dar al Gani 476, the 13th martian meteorite, was recovered from the Sahara in 1998. It is a basaltic shergottitic rock composed of olivine megacrysts reaching 5 mm (24 vol%) set in a finegrained groundmass of pyroxene (59 vol%) and maskelynitized plagioclase (12 vol%) with minor amounts of accessory phases (spinel, merrillite, ilmenite). Dar al Gani 476 is similar to lithology A of Elephant Moraine A79001 (EETA79001) in petrography and mineralogy, but is distinct in several aspects. Low‐Ca pyroxenes in the Dar al Gani 476 groundmass are more magnesian (En76Fs21 Wo3～En58Fs30Wo12) than those in lithology A of EETA79001 (En73Fs22Wo5～En45Fs43Wo12), rather similar to pyroxenes in lherzolitic martian meteorites (En76Fs21 Wo3～En63Fs22Wo15). Dar al Gani 476 olivine is less magnesian and shows a narrower compositional range (Fo76‐58) than EETA79001 olivine (Fo81‐53), and is also similar to olivines in lherzolitic martian meteorites (Fo74‐65). The orthopyroxene‐olivine‐chromite xenolith typical in the lithology A of EETA79001 is absent in Dar al Gani 476. It seems that Dar al Gani 476 crystallized from a slightly more primitive mafic magma than lithology A of EETA79001 and several phases (olivine, pyroxene, chromite, and ilmenite) in Dar al Gani 476 may have petrogenetic similarities to those of lherzolitic martian meteorites. Olivine megacrysts in Dar al Gani 476 are in disequilibrium with the bulk composition. The presence of fractured olivine grains in which the most Mg‐rich parts are in contact with the groundmass suggests that little diffusive modification of original olivine compositions occurred during cooling. This observation enabled us to estimate the cooling rates of Dar al Gani 476 and EETA79001 olivines, giving similar cooling rates of 0.03‐3 °C/h for Dar al Gani 476 and 0.05‐5 °C/h for EETA79001. This suggests that they were cooled near the surface (burial depth shallower than about 3 m at most), probably in lava flows during crystallization of groundmass. As is proposed for lithology A of EETA79001, it may be possible to consider that Dar al Gani 476 has an impact melt origin, a mixture of martian lherzolite and other martian rock (Queen Alexandra Range 94201, nakhlites?).  相似文献   

7.
Abstract— A number of martian meteorite samples contain secondary alteration minerals such as Ca‐Mg‐Fe carbonates, Fe oxides, and clay minerals. These mineral assemblages hint at hydrothermal processes occurring in the martian crust, but the alteration conditions are poorly constrained. This study presents the results of experiments that examined the alteration of a high‐Fe basalt by CO2‐saturated aqueous fluids at 23 and 75 °C and by mixed H2O‐CO2 vapors at 200 and 400 °C and water‐rock ratios of 1:1 and 1:10. Results indicate that observable alteration of the basalt takes place after runs of only seven days. This alteration includes mobilization of silica into phases such as opal‐CT and quartz, as well as the formation of carbonates, oxides, and at some conditions, zeolites and hydrous silicates. The degree of alteration increases with run temperature and, in high‐temperature vapor experiments, with increasing water content of the vapor. The degree of alteration and the mineralogy observed in the martian meteorites suggests that none of these samples were exposed to aqueous fluids for long periods of time. Nakhla and Lafayette probably interacted with water for relatively brief periods of time; if so, silica may have been leached from the parent rocks by the altering fluids. Allan Hills 84001 shows possible evidence for very limited interaction with an aqueous fluid, but the overall slight degree of alteration described for this meteorite strongly suggests that it never interacted extensively or at high temperature with any water‐bearing fluid. Elephant Moraine A79001 may not have been altered by aqueous fluids at all. The results of this study best support models wherein the meteorite parent rocks were wetted intermittently or for brief periods of time rather than models that invoke long‐term reaction with large volumes of water. Our experiments studied alteration of a high‐Fe basalt by dilute, CO2‐saturated, aqueous solutions at 23 and 75 °C and by mixed H2O‐CO2 vapors at 200 and 400 °C. The results suggest that alteration of the parent rock takes place even after very short reaction times of seven days. All experiments produced carbonate minerals, including calcite, and in some cases, magnesite, siderite, and ankerite. A free silica phase, either opal, quartz, or hydrated silica, formed in most experiments. More altered experiments also contained minerals such as zeolites and hydrous phyllosilicates. Clay minerals were not observed to form in any experiments. In aqueous fluids, higher temperature corresponded with a higher degree of alteration, whereas changing fluid composition had no observable effect. In high‐temperature vapors, the degree of alteration was controlled by temperature and the proportion of H2O to CO2, with water‐rock ratio also playing a role in transport of silica. Application of these results to martian meteorites that contain secondary alteration minerals suggests that none of the martian rocks underwent extensive interaction with aqueous fluids. Nakhla and Lafayette contain clay minerals, which suggests that they interacted with water to some extent, possibly at elevated temperatures. Although ALH84001 shows possible evidence of very limited interaction with aqueous fluids, EETA79001 does not. These results support models for the alteration of these meteorites that do not invoke long‐term interaction with water or reaction with large volumes of water. Except for some models for alteration of ALH84001, this conclusion agrees with most of the literature on alteration of martian meteorites.  相似文献   

8.
Abstract— Scanning electron microscopy and energy-dispersive X-ray spectrometry of untreated interior chips from three different specimens of the Chassigny meteorite confirm the presence of discrete grains of Ca-carbonate, Mg-carbonate, and Ca-sulfate. Morphologies of these salt grains suggest that the Ca-carbonate is calcite (CaCO3) and that the Ca-sulfate is gypsum (CaSO4·2H2O) or bassanite (CaSO4·1/2H2O). The morphologic identification of the Mg-carbonate is equivocal, but rhombohedral and acicular crystal habits suggest magnesite and hydromagnesite, respectively. The salts in Chassigny occur as discontinuous veins in primary igneous minerals and are similar to those previously documented in the nakhlites, Nakhla and Lafayette, and in shergottite EETA79001. Unlike those in nakhlites, however, the Chassigny salts occur alone, without associated ferric oxides or aluminosilicate clays. Traces of Cl and P in Chassigny salts are consistent with precipitation of the salts from short-lived, saline, aqueous solutions that postdated igneous crystallization. In contrast with the clear case for nakhlites, stratigraphic evidence for a preterrestrial origin of the salts in Chassigny is ambiguous; however, a preterrestrial origin of the Chassigny salts best explains all available evidence. The water-precipitated salts provide clear physical evidence for the hypothesis, proposed by other workers, that the igneous amphiboles in Chassigny might have experienced isotope-exchange reactions with near-surface water, thereby compromising the original stable-isotope signature of any magmatic water in melt inclusions.  相似文献   

9.
Abstract— Considerable evidence points to a martian origin of the SNC meteorites. Noble gas isotopic compositions have been measured in most SNC meteorites. The 129Xe/132Xe vs. 84Kr/132Xe ratios in Chassigny, most shergottites, and lithology C of EETA 79001 define a linear array. This array is thought to be a mixing line between martian mantle and martian atmosphere. One of the SNC meteorites, Nakhla, contains a leachable component that has an elevated 129Xe/132Xe ratio relative to its 84Kr/132Xe ratio when compared to this approximately linear array. The leachable component probably consists in part of iddingsite, an alteration product produced by interaction of olivine with aqueous fluid at temperatures lower than 150 °C. The elevated Xe isotopic ratio may represent a distinct reservoir in the martian crust or mantle. More plausibly, it is elementally fractionated martian atmosphere. Formation of sediments fractionates the noble gases in the correct direction. The range of sediment/atmosphere fractionation factors is consistent with the elevated 129Xe/132Xe component in Nakhla being contained in iddingsite, a low temperature weathering product. The crystallization age of Nakhla is 1.3 Ga. Its low-shock state suggests that it was ejected from near the surface of Mars. As liquid water is required for the formation of iddingsite, these observations provide further evidence for the near surface existence of aqueous fluids on Mars more recently than 1.3 Ga.  相似文献   

10.
Abstract— Isotopic analysis of nesquehonite recovered from the surface of the LEW 85320 H5 ordinary chondrite shows that the δ13C and δ18O values of the two generations of bicarbonate (Antarctic and Texas) are different: δ13C = +7.9‰ and +4.2‰; δ18O = +17.9‰ and + 12.1‰ respectively. Carbon isotopic compositions are consistent with equilibrium formation from atmospheric carbon dioxide at ?2 ± 4 °C (Antarctic) and +16 ± 4 °C (Texas). Oxygen isotopic data imply that the water required for nesquehonite precipitation was derived from atmospheric water vapour or glacial meltwater which had locally exchanged with silicates, either in the meteorite or in underlying bedrock. Although carbonates with similar δ13C values have been identified in the SNC meteorites EETA 79001 and Nakhla, petrographic and temperature constraints argue against their simply being terrestrial weathering products.  相似文献   

11.
Abstract— In 1998, Dar al Gani (DaG) 476 was found in the Libyan desert. The meteorite is classified as a basaltic shergottite and is only the 13th martian meteorite known to date. It has a porphyritic texture consisting of a fine‐grained groundmass and larger olivines. The groundmass consists of pyroxene and feldspathic glass. Minor phases are oxides and sulfides as well as phosphates. The presence of olivine, orthopyroxene, and chromite is a feature that DaG 476 has in common with lithology A of Elephant Moraine (EET) A79001. However, in DaG 476, these phases appear to be early phenocrysts rather than xenocrysts. Shock features, such as twinning, mosaicism, and impact‐melt pockets, are ubiquitous. Terrestrial weathering was severe and led to formation of carbonate veins following grain boundaries and cracks. With a molar MgO/(MgO + FeO) of 0.68, DaG 476 is the most magnesian member among the basaltic shergottites. Compositions of augite and pigeonite and some of the bulk element concentrations are intermediate between those of lherzolitic and basaltic shergottites. However, major elements, such as Fe and Ti, as well as LREE concentrations are considerably lower than in other shergottites. Noble gas concentrations are low and dominated by the mantle component previously found in Chassigny. A component, similar to that representing martian atmosphere, is virtually absent. The ejection age of 1.35 ± 0.10 Ma is older than that of EETA79001 and could possibly mark a distinct ejection. Dar al Gani 476 is classified as a basaltic shergottite based on its mineralogy. It has a fine‐grained groundmass consisting of clinopyroxene, pigeonite and augite, feldspathic glass and chromite, Ti‐chromite, ilmenite, sulfides, and whitlockite. Isolated olivine and single chromite grains occur in the groundmass. Orthopyroxene forms cores of some pigeonite grains. Shock‐features, such as shock‐twinning, mosaicism, cracks, and impact‐melt pockets, are abundant. Severe weathering in the Sahara led to significant formation of carbonate veins crosscutting the entire meteorite. Dar al Gani 476 is distinct from other known shergottites. Chemically, it is the most magnesian member among known basaltic shergottites and intermediate in composition for most trace and major elements between Iherzolitic and basaltic shergottites. Unique are the very low bulk REE element abundances. The CI‐normalized abundances of LREEs are even lower than those of Iherzolitic shergottites. The overall abundance pattern, however, is similar to that of QUE 94201. Textural evidence indicates that orthopyroxene, as well as olivine and chromite, crystallized as phenocrysts from a magma similar in composition to that of bulk DaG 476. Whether such a magma composition can be a shergottite parent melt or was formed by impact melting needs to be explored further. At this time, it cannot entirely be ruled out that these phases represent relics of disaggregated xenoliths that were incorporated and partially assimilated by a basaltic melt, although the texture does not support this possibility. Trapped noble gas concentrations are low and dominated by a Chassigny‐like mantle component. Virtually no martian atmosphere was trapped in DaG 476 whole‐rock splits. The exposure age of 1.26 ± 0.09 Ma is younger than that of most shergottites and closer to that of EETA79001. The ejection age of 1.35 ± 0.1 Ma could mark another distinct impact event.  相似文献   

12.
Abstract— Dar al Gani 489 (DaG 489) is a meteorite fragment of 2146 g found in the Libyan Sahara by a meteorite finder during one of his search campaigns in 1997–98. It is a porphyritic rock with millimetersized olivine crystals (Fo79–59) set in a fine‐grained groundmass (average grain size 0.1 mm) consisting of pigeonite (En75–57 Wo5–15) crystals and interstitial feldspathic glass (An67–56 Or0–1). Minor phases include enstatite (En82–71 Wo2–4), augite (En48–52 Wo29–32), chromite, Ti‐chromite, ilmenite, pyrrhotite, merrillite, and secondary calcite and iron oxides. On the basis of mineralogical, petrographic, bulk chemical, O‐isotopic, and noble gas data, DaG 489 can be classified as a highly shocked martian meteorite (e.g., Fe/Mn(bulk) = 42.1, Ni/Mg(bulk) = 0.002; δ17O = 2.89, δ18O = 4.98, and Δ17O = 0.305), belonging to the basaltic shergottite subgroup. The texture and modal composition of DaG 489 are indeed those of basalts; nonetheless, the bulk chemistry, the abundance of large olivine and chromite crystals, and enstatitic pyroxene suggest some relationship with lherzolitic shergottites. As such, DaG 489 is similar to the hybrid shergottite Elephant Moraine (EET) A79001 lithology A; however, there are some relevant differences including a higher olivine content (20 vol%), the lack of orthopyroxene megacrysts, a higher molar Mg/(Mg + Fe)(molar) = 0.68, and a lower rare earth element content in the bulk sample. Therefore, DaG 489 has the potential of providing us with a further petrogenetic link between the basaltic and lherzolitic shergottites. Noble gases data show that DaG 489 has an ejection age of ～1.3 Ma. This young age lends support to the requirement of several ejection events to produce the current population of shergottites, nakhlites, and chassignites (SNC) meteorites. In terms of texture, mineral and bulk compositions, shock level, and weathering features, DaG 489 is essentially identical to DaG 476, another basaltic shergottite independently found ～25 km due northnortheast of DaG 489. Because DaG 489 also has the same exposure history as DaG 476, it is very likely that both meteorites are fragments of the same fall. In addition to the existing hypotheses on the petrogenesis of the similar EETA79001 lithology A and the identical DaG 476, we propose that DaG 489 could have formed through high‐degree partial melting of a lherzolite‐like material.  相似文献   

13.
The isotopic composition and abundance of sulfur in extraterrestrial materials are of interest for constraining models of both planetary and solar system evolution. A previous study that included phase‐specific extraction of sulfur from 27 shergottites found the sulfur isotopic composition of the Martian mantle to be similar to that of terrestrial mid‐ocean ridge basalts, the Moon, and nonmagmatic iron meteorites. However, the presence of positive Δ33S anomalies in igneous sulfides from several shergottites, indicating incorporation of atmospherically processed sulfur into the subsurface, complicated this interpretation. The current study expands upon the previous work through analyses of 20 additional shergottites, enabling tighter constraints on the isotopic composition of juvenile Martian sulfur. The updated composition (δ34S = ?0.24 ± 0.05‰, Δ33S = 0.0015 ± 0.0016‰, and Δ36S = 0.039 ± 0.054‰, 2 s.e.m.), representing the weighted mean for all shergottites within the combined population of 47 without significant Δ33S anomalies, strengthens our earlier result. The presence of sulfur isotopic anomalies in igneous sulfides of some meteorites suggests that their parent magmas may have assimilated crustal material. We observed small negative Δ33S anomalies in sulfides from two meteorites, NWA 7635 and NWA 11300. Although negative Δ33S anomalies have been observed in nakhlites and ALH 84001, previous anomalies in shergottites have all shown positive values of Δ33S. Because NWA 7635 has formation age of 2.4 Ga and is much more ancient than shergottites analyzed previously, this finding expands our perspective on the continuity of Martian atmospheric sulfur photochemistry over geologic time.  相似文献   

14.
Abstract– Xenon‐isotopic ratios, step‐heating release patterns, and gas concentrations of mineral separates from Martian shergottites Roberts Massif (RBT) 04262, Dar al Gani (DaG) 489, Shergotty, and Elephant Moraine (EET) 79001 lithology B are reported. Concentrations of Martian atmospheric xenon are similar in mineral separates from all meteorites, but more weathered samples contain more terrestrial atmospheric xenon. The distributions of xenon from the Martian and terrestrial atmospheres among minerals in any one sample are similar, suggesting similarities in the processes by which they were acquired. However, in opaque and maskelynite fractions, Martian atmospheric xenon is released at higher temperatures than terrestrial atmospheric xenon. It is suggested that both Martian and terrestrial atmospheric xenon were initially introduced by weathering (low temperature alteration processes). However, the Martian component was redistributed by shock, accounting for its current residence in more retentive sites. The presence or absence of detectable 129Xe from the Martian atmosphere in mafic minerals may correspond to the extent of crustal contamination of the rock’s parent melt. Variable contents of excess 129Xe contrast with previously reported consistent concentrations of excess 40Ar, suggesting distinct sources contributed these gases to the parent magma.  相似文献   

15.
Abstract— Measured Ne isotopes in samples of shergottite ALHA77005 show variations in 21Ne/22Ne ratios and 21Ne abundances that are consistent with the presence of two cosmogenic components: a component produced by nuclear interactions of galactic cosmic rays (GCR) and a component produced at shallow shielding depths (～0–3 cm) by energetic solar flare protons (SCR). We suggest that the 21Ne/22Ne ratio generally can be used to distinguish between SCR and GCR components in many meteorite types. Analysis of cosmogenic Ne produced in chondrite mineral separates, eucrites, and anorthositic lunar rocks, all having diverse major element compositions, indicate that the GCR 21Ne/22Ne ratio increases modestly with relative Mg content. Data for hundreds of chondrite analyses suggest that SCR Ne is present in no more than a very small fraction of chondrites. Examination of literature data for other shergottites, however, indicate that all of these meteorites contain SCR Ne but that it is apparently absent in other SNC meteorites. The ubiquitous presence of SCR Ne in shergottites, in contrast to most other types of meteorites, suggests that the martian origin of shergottites gave them different orbital parameters compared to other meteorites. This in turn may have contributed to slower entry velocities and lesser surface ablation in the atmosphere or even to higher SCR production rates.  相似文献   

16.
Abstract— The enrichment of F on Antarctic meteorites is the result of their exposure to the atmosphere, and its measurement allows a subdivision of the terrestrial age into a duration of exposure on the ice and the time a meteorite was enclosed by the ice. In many cases, the periods of surface exposure are only small fractions of the terrestrial ages of meteorites collected in Antarctica. The enrichment of F on the surfaces of Antarctic achondrites was investigated by means of nuclear reaction analysis (NRA): scanning proton beams with an energy of 2.7 and 3.4 MeV were used to induce the reactions 19F(p,αγ)16O and 19F(p, p'γ)19F, respectively. Gamma signals proportional to the F content were measured. The following Antarctic achondrites were investigated: Martian meteorite ALH 84001; diogenite ALHA77256; the eucrites ALHA81011 and ALHA78132; and in addition, the H5 chondrite ALHA79025. For ALH 84001, our data indicate a period of exposure on the ice of <500 years. Thus, this specimen was enclosed in the ice >95% of its terrestrial age of 13 000 years.  相似文献   

17.
We present a methodology to build a reduced chemical scheme adapted to the study of hydrocarbons in the atmospheres of giant planets and Titan. As an example, we have built a reduced chemical scheme, containing only 25 compounds and 46 reactions (including photolysis), which is well adapted to compute the abundance of the main hydrocarbons observed so far in the atmosphere of Saturn (CH3, CH4, C2H2, C2H4, C2H6, CH3C2H, C3H8 and C4H2). This scheme gives similar results, within the error bars of the model, as a 1D photochemical model using an initial chemical scheme containing 90 compounds and more than 600 reactions. As a consequence, such a methodology can be used to build a reduced scheme well adapted to future 2D (or 3D) photochemical models and GCMs.  相似文献   

18.
Carbon and nitrogen data from stepped combustion analysis of eight angrites, seven eucrites, and two diogenites, alongside literature data from a further nine eucrites and two diogenites, have been used to assess carbon and nitrogen incorporation and isotope fractionation processes on the angrite parent body (APB), for comparison with volatile behavior on the HED parent body (4 Vesta). A subset of the angrite data has been reported previously (Abernethy et al. 2013 ). Two separate families of volatile components were observed. They were (1) moderately volatile material (MVM), mostly combusting between ~500 and 750 °C and indistinguishable from terrestrial contamination and (2) refractory material (RM), mainly released above 750 °C and thought to be carbon (as ) and nitrogen (as N2 or ) dissolved within the silicate lattice, fitting with the slightly oxidized (~IW to IW+2) angrite fO2 conditions. Isotopic fractionation trends for carbon and nitrogen within the plutonic and basaltic (quenched) angrites suggest that the behavior of the two volatile elements is loosely coupled, but that the fractionation process differs between the two angrite subgroups. Comparison with results from eucrites and diogenites implies similarities between speciation of carbon and nitrogen on 4 Vesta and the APB, with the latter being more enriched in volatiles than the former.  相似文献   

19.
Abstract— We report the results of a study of a halite-siderite-anhydrite-chlorapatite assemblage in the Shergotty-Nakhla-Chassigny (SNC) Martian meteorite Nakhla. These minerals are found associated with each other in interstitial areas, with halite often being adjacent to or enclosing siderite. We suggest the halite and other minerals are Martian in origin because (1) the conditions of fall preclude significant amounts of terrestrial contamination or weathering having taken place; (2) textures indicate that the minerals within this assemblage crystallized at the same stage as some silicate and oxide minerals within the Nakhla parent; and (3) the association with siderite, which previous studies have shown has C and O-isotopic compositions incompatible with an origin on the Earth. Siderite has the range of compositions: CaCO3, 0.1–5.7; MgCO3, 2.0–40.9; FeCO3, 23.2–87.0; MnCO3, 1.0–39.9 mol%. There are two compositional groupings: high-MnCO3 (≥30 mol%) and low-MnCO3/high-FeCO3, with a gap identified between the two. This may be a miscibility gap or, alternatively, the two compositional groupings may mark separate generations of carbonate. We have not found any textural evidence for the latter explanation, but acceptance of the presence of a miscibility gap would require independent work on Fe-Mn carbonates to verify its existence. Trace element abundances have been determined by ion microprobe analysis on three siderite and one anhydrite grains. Siderite has light rare earth elements (2.2–7.3 × C1) greater than heavy rare earth elements (0.32–0.79 × C1) without Ce or Eu anomalies, and the anhydrite has a similar pattern. These abundances reflect the source composition rather than partitioning or complexing controls. They are not typical of hydrothermal signatures which generally do not have such smooth REE abundance patterns. The nature of the mineral assemblage suggests that its source rocks on Mars were evaporites. These may be common in the craters and flood plains of the Martian southern highlands. Two models are suggested in this paper to explain the incorporation of evaporitic material into the Nakhla igneous parent. It may have happened as a low-temperature process (<200 °C) by crystallisation from an aqueous fluid. An origin at low temperature is compatible with the available experimental data on siderite stability. Alternatively, we suggest evaporitic material may have been incorporated into the Nakhla parent while melt was still present and crystallized ～800 °C. The latter model can more readily explain the trace element abundances and also the siderite textures that imply intergrowth with residual interstitial melt. Both high- and low-temperature models are consistent with the presence of evaporite sediments on Mars.  相似文献   

20.
Volatile elements play a key role in the dynamics of planetary evolution. Extensive work has been carried out to determine the abundance, distribution, and source(s) of volatiles in planetary bodies such as the Earth, Moon, and Mars. A recent study showed that the water in apatite from eucrites has similar hydrogen isotopic compositions compared to water in terrestrial rocks and carbonaceous chondrites, suggesting that water accreted very early in the inner solar system given the ancient crystallization ages (~4.5 Ga) of eucrites. Here, the measurements of water (reported as equivalent H2O abundances) and the hydrogen isotopic composition (δD) of apatite from five basaltic eucrites and one cumulate eucrite are reported. Apatite H2O abundances range from ~30 to ~3500 ppm and are associated with a weighted average δD value of ?34 ± 67‰. No systematic variations or correlations are observed in H2O abundance or δD value with eucrite geochemical trend or metamorphic grade. These results extend the range of previously published hydrogen isotope data for eucrites and confirm the striking homogeneity in the H‐isotopic composition of water in eucrites, which is consistent with a common source for water in the inner solar system.  相似文献   

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