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1.
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   

2.
Degassed magmatic water was potentially the major source of surficial water on Mars. We measured Li, B, and Be abundances and Li isotope profiles in pyroxenes, olivines, and maskelynite from four compositionally different shergottites—Shergotty, QUE 94201, LAR 06319, and Tissint—using secondary ion mass spectrometry (SIMS). All three light lithophile elements (LLE) are incompatible: Li and B are soluble in H2O‐rich fluids, whereas Be is insoluble. In the analyzed shergottites, Li concentration decreases and Be concentration increases from cores to rims in pyroxenes. However, B concentrations do not vary consistently with Li and Be abundances, except in QUE 94201 pyroxenes. Additionally, abundances of these three elements in olivines show a normal igneous‐fractionation trend consistent with the crystallization of olivine before magma ascent and degassing. We expect that kinetic effects would lead to fractionation of 6Li in the vapor phase compared to 7Li during degassing. The Li isotope profiles, with increasing δ7Li from cores to rims, as well as Li and B profiles indicate possible degassing of hydrous fluids only for the depleted shergottite QUE 94201, as also supported by degassing models. Conversely, Shergotty, LAR 06319, and Tissint appear to have been affected by postcrystallization diffusion, based on their LLE and Li isotope profiles, accompanied by diffusion models. This process may represent an overlay on a degassing pattern. The LLE profiles and isotope profiles in QUE 94201 support the hypothesis that degassing of some basaltic shergottite magmas provided water to the Martian surface, although evidence may be obscured by subsolidus diffusion processes.  相似文献   

3.
Abstract— Antarctic meteorite Queen Alexandra Range (QUE) 94201 is a 12 g basaltic achondrite dominated by plagioclase (now maskelynite) and zoned low‐ and high‐Ca pyroxene. Petrologic, geochemical, and isotopic analyses indicate that it is related to previously described basaltic and Iherzolitic shergottites, which are a group of igneous meteorites that are believed to be from Mars. Unlike previous shergottites, however, QUE 94201 represents a bulk melt rather than a cumulate fraction, meaning it can be used to infer magmatic source regions and the compositions of other melts on Mars. This melt has much more Fe and P than basaltic melts produced on Earth and formed at a much lower oxygen fugacity. This has altered the crystallization sequence of the melt, removing olivine from the liquidus to produce a plagioclase and 2‐pyroxene assemblage. If the high‐phosphorus and low‐oxygen fugacity conditions represented by QUE 94201 are common in magmatic regions of Mars, then olivine may be rare in marrian basalts. No solar cosmic ray effects were seen in the concentrations of 10Be, 26A1, and 36C1 with depth in the meteorite, implying at least 3 cm of ablation during entry to Earth. Significant excesses of neutron capture noble gas isotopes (80,82Kr and 128,131Xe) suggest that the QUE 94201 sample came from a depth >22 cm in a meteoroid of at least that radius. The meteorite also has very low 21Ne/22Ne, which would often be interpreted to mean little ablation (contradicting above evidence) but, in this case, appears to reflect a very low abundance of Mg (the principal target element for Ne) in the meteorite, consistent with our bulk chemical analyses. The meteorite has a terrestrial 36C1 age of 0.29 ± 0.05 Myr and a 10Be exposure age of 2.6 ± 0.5 Myr in a 47π geometry, implying an ejection age of 2.9 ± 0.5 Myr.  相似文献   

4.
Abstract— North West Africa (NWA) 480 is a new martian meteorite of 28 g found in the Moroccan Sahara in November 2000. It consists mainly of large gray pyroxene crystals (the largest grains are up to 5 mm in length) and plagioclase converted to maskelynite. Excluding the melt pocket areas, modal analyses indicate the following mineral proportions: 72 vol% pyroxenes extensively zoned, 25% maskelynite, 1% phosphates (merrillite and chlorapatite), 1% opaque oxides (ilmenite, ulvöspinel and chromite) and sulfides, and 1% others such as silica and fayalite. The compositional trend of NWA 480 pyroxenes is similar to that of Queen Alexandra Range (QUE) 94201 but in NWA 480 the pyroxene cores are more Mg‐rich (En77‐En65). Maskelynites display a limited zoning (An42–50Ab54‐48Or2–4). Our observations suggest that NWA 480 formed from a melt with a low nuclei density at a slow cooling rate. The texture was achieved via a single‐stage cooling where pyroxenes grew continuously. A similar model was previously proposed for QUE 94201 by McSween et al. (1996). NWA 480 is an Al‐poor ferroan basaltic rock and resembles Zagami or Shergotty for major elements and compatible trace element abundances. The bulk rock analysis for oxygen isotopes yields Δ17O = +0.42%, a value in agreement at the high margin, with those measured on other shergottites (Clayton and Mayeda, 1996; Romanek et al., 1998; Franchi et al., 1999). Its CI‐normalized rare earth element pattern is similar to those of peridotitic shergottites such as Allan Hills (ALH)A77005, suggesting that these shergottites shared a similar parent liquid, or at least the same mantle source.  相似文献   

5.
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   

6.
Abstract— We present the results of a combined mineralogic‐petrologic and ion microprobe study of two martian meteorites recently recovered in the Lybian Sahara, Dar al Gani 476 (DaG 476) and Dar al Gani 489 (DaG 489). Having resided in a hot desert environment for an extended time, DaG 476 and DaG 489 were subjected to terrestrial weathering that significantly altered their chemical composition. In particular, analyses of some of the silicates show light rare earth element (LREE)‐enrichment resulting from terrestrial alteration. In situ measurement of trace element abundances in minerals allows us to identify areas unaffected by this contamination and, thereby, to infer the petrogenesis of these meteorites. No significant compositional differences between DaG 476 and DaG 489 were found, supporting the hypothesis that they belong to the same fall. These meteorites have characteristics in common with both basaltic and lherzolitic shergottites, possibly suggesting spatial and petrogenetic associations of these two types of lithologies on Mars. However, the compositions of Fe‐Ti oxides and the size of Eu anomalies in the earliest‐formed pyroxenes indicate that the two Saharan meteorites probably experienced more reducing crystallization conditions than other shergottites (with the exception of Queen Alexandra Range (QUE) 94201). As is the case for other shergottites, trace element microdistributions in minerals of the DaG martian meteorites indicate that closed‐system crystal fractionation from a LREE‐depleted parent magma dominated their crystallization history. Furthermore, rare earth element abundances in the orthopyroxene megacrysts are consistent with their origin as xenocrysts rather than phenocrysts.  相似文献   

7.
We present a study of the petrology and geochemistry of basaltic shergottite Northwest Africa 2975 (NWA 2975). NWA 2975 is a medium‐grained basalt with subophitic to granular texture. Electron microprobe (EMP) analyses show two distinct pyroxene compositional trends and patchy compositional zoning patterns distinct from those observed in other meteorites such as Shergotty or QUE 94201. As no bulk sample was available to us for whole rock measurements, we characterized the fusion crust and its variability by secondary ion mass spectrometer (SIMS) measurements and laser ablation inductively coupled plasma spectroscopy (LA‐ICP‐MS) analyses as a best‐available proxy for the bulk rock composition. The fusion crust major element composition is comparable to the bulk composition of other enriched basaltic shergottites, placing NWA 2975 within that sample group. The CI‐normalized REE (rare earth element) patterns are flat and also parallel to those of other enriched basaltic shergottites. Merrillite is the major REE carrier and has a flat REE pattern with slight depletion of Eu, parallel to REE patterns of merrillites from other basaltic shergottites. The oxidation state of NWA 2975 calculated from Fe‐Ti oxide pairs is NNO‐1.86, close to the QFM buffer. NWA 2975 represents a sample from the oxidized and enriched shergottite group, and our measurements and constraints on its origin are consistent with the hypothesis of two distinct Martian mantle reservoirs: a reduced, LREE‐depleted reservoir and an oxidized, LREE‐enriched reservoir. Stishovite, possibly seifertite, and dense SiO2 glass were also identified in the meteorite, allowing us to infer that NWA 2975 experienced a realistic shock pressure of ~30 GPa.  相似文献   

8.
We report the results of nominally anhydrous equilibrium and fractional crystallization experiments on a synthetic Yamato‐980459 (Y98) bulk composition at 0.5 GPa. These experiments allow us to test a suggested fractional crystallization model, calculated using MELTS by Symes et al. ( 2008 ), in which a Y98‐like initial liquid yielded a magma closely resembling the bulk composition of QUE 94201. Although the two meteorites cannot be cogenetic owing to their age difference, they are thought to represent bona fide magmatic liquids rather than products of crystal accumulation, as are most Martian basaltic meteorites. Hence, understanding possible petrogenetic links between these types of liquids could be revealing about processes of melting and crystallization that formed the range of Martian basalts. We find that Y98 can, in fact, generate a residual liquid closely resembling QUE, but only after a very different crystallization process, and different degree of crystallization, than that modeled using MELTS. In addition, both the identity and sequence of crystallizing phases are very different between model and experiments. Our fractional crystallization experiments do not produce a QUE‐like liquid, and the crystallizing phases are an even poorer match to the MELTS‐calculated compositions than in the equilibrium runs. However, residual liquids from our experiments define a liquid line of descent that encompasses bulk compositions of parental melts calculated for several Martian basaltic meteorites, suggesting that the known Martian basaltic meteorites had their ultimate origin from the same or very similar source lithologies. These are, in turn, similar to source rocks modeled by previous studies as products of extensive crystallization of an initial Martian magma ocean.  相似文献   

9.
Abstract— Isotopic abundances of the noble gases were measured in the following Martian meteorites: two shock glass inclusions from Elephant Moraine (EET) 79001, shock vein glass from Shergotty and Yamato (Y) 793605, and whole-rock samples of Allan Hills (ALH) 84001 and Queen Alexandra Range (QUE) 94201. These glass samples, when combined with literature data on a separate single glass inclusion from EET 79001 and a glass vein from Zagami, permit examination in greater detail of the isotopic composition of Ne, Ar, Kr, and Xe trapped from the Martian atmosphere. The isotopic composition of Martian Ne, if actually present in these glasses, remains poorly defined. The 40Ar/36Ar ratio of trapped Martian atmospheric Ar is probably considerably lower than the nominal ratio of 3000 measured by Viking, and data on impact glasses suggest a value of ～1900. The atmospheric 36Ar/38Ar ratio is ≤4.0. Martian atmospheric Kr may be enriched in lighter isotopes by ～0.5%/amu compared to both solar-wind Kr and to the Martian composition previously reported. The isotopic composition of Xe in these glasses agrees with that previously reported in the literature. The Martian atmospheric 36Ar/132Xe and 84Kr/132Xe elemental ratios are higher than those reported by Viking by factors of ～2.5–1.6 (depending on the 40Ar/36Ar ratio adopted) and ～1.8, respectively, and are discussed in a separate paper. Cosmogenic gases indicate space exposure ages of 2.7 ± 0.6 Ma for QUE 94201 and Shergotty and 14 ± 1 Ma for ALH 84001. Small amounts of 21Ne produced by energetic solar protons may be present in QUE 94201 but are not present in ALH 84001 or Y-793605. The space exposure age for Y-793605 is 4.9 ± 0.6 Ma and appears to be distinctly older than the ages for basaltic shergottites. However, uncertainties in cosmogenic production rates still makes somewhat uncertain the number of Martian impact events required to produce the exposure ages of Martian meteorites.  相似文献   

10.
Abstract— We compare and contrast the mineralogy and petrology of the 2 stones of the extremely ferroan and Cr‐poor martian meteorite, Los Angeles. The 2 stones are similar in many characteristics, strongly suggesting that they originated from a single flow or shallow intrusion. However, stone 2 is more ferroan and enriched in late‐stage materials than its larger, and more widely studied, sibling. Stone 2 has a far higher abundance (?25 vol%) than stone 1 (10 vol%) of combined “opaques,” meaning not only conventional opaque minerals but also, and more abundantly, fine‐grained symplectitic intergrowths of fayalite + ferroan augite + silica (interpreted as pyroxferroite breakdown material, PBM). The bulk composition of the PBM is close to that of stoichiometric pyroxferroite, with roughly 45 wt% FeO. Extensive zonation within the pyroxenes of both stones is consistent with origin by closed‐system fractional crystallization of the parent basaltic melt(s). However, the compositional and modal disparity between the two stones suggests that they formed in an environment where at least mild multi‐cm‐scale differentiation occurred. Probably, in both stones, crystallization began from similar melts with mg ?27–28 mol%, but during crystallization, significant migration of the melt component occurred, perhaps by crystal settling and/or filter pressing. Stone 2 acquired an enhanced proportion of residual melt and, thus, higher proportions of late‐stage materials such as PBM, oxides, and phosphates. Within the PBM, clinopyroxene poikiloblastically encloses fayalite and silica. At least some of the PBM had already formed by decomposition of pyroxferroite before the major shock that caused the very scarce brecciation within Los Angeles. However, the low abundance of fractures within PBM, in comparison to pyroxene and some other minerals, may be an indication that the textures of PBM regions typically did not assume their final detailed configuration until after the last major shock. The steep slope of a pyroxene mg‐Cr correlation suggests that igneous crystallization occurred at higher fO2 in Los Angeles than in otherwise similar shergottites such as QUE 94201, Shergotty, and Zagami.  相似文献   

11.
Abstract— Quantitative petrographic analysis, using the crystal size distribution (CSD) method, provides a novel approach for examining the crystallization histories of basaltic shergottites. Grain number densities at different sizes are plotted against grain size, and the resulting curve relates to the geologic processes involved with the crystallization of the grain population. Most basaltic shergottites are dominated by pigeonite and augite; and because plagioclase is primarily interstitial, and therefore constrained in its growth by the surrounding pyroxenes, we limited our size measurements to the pyroxene phases. The groundmasses of Elephant Moraine (EET) A79001 lithology A and Dar al Gani (DaG) 476 are fine grained with cumulus pyroxene and interstitial plagioclase glass. Their simple linear CSD plots record a single stage of pyroxene crystallization under steady‐state conditions of continuous nucleation and growth. The textures of Queen Alexandra Range (QUE) 94201 and EETA79001 lithology B are quite different from the other shergottites, with intergrown pyroxene and plagioclase. Likewise, their CSD plots are also distinct, with curved trends that suggest a lack of large grains, most likely because of interference between simultaneously growing silicate phases. However, the CSD plot shapes are smooth, also implying a single stage of growth. Shergotty and Zagami, with coarser cumulus textures, display CSD plots that are generally linear over most grain sizes. This implies that conditions of nucleation and growth were dominant during formation of the pyroxene populations. Both plots, however, also display kinks, implying multiple stages of growth. A similar kink is also visible in a CSD plot of only the Mg‐rich cores of Shergotty pyroxenes, which suggests the feature represents changes in conditions during core crystallization, rather than an event coincident with the change in composition to the Fe‐rich rims. The plot may be interpreted as representing two stages of core growth with an intervening short hiatus of nucleation, with continued crystallization associated with ascent of the magma. Eruption onto the surface probably triggered the compositional change to Fe‐rich rims. The CSD analysis of products from a controlled crystallization study agree with experimental and petrologic estimates that cooling rates for Zagami were on the order of a few tenths of a degree per hour. Growth rates derived from these cooling rates suggest crystallization of Shergotty and Zagami pyroxenes occurred over a period of a few weeks to months.  相似文献   

12.
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   

13.
Abstract– The Opportunity rover of the Mars Exploration Rover mission encountered an isolated rock fragment with textural, mineralogical, and chemical properties similar to basaltic shergottites. This finding was confirmed by all rover instruments, and a comprehensive study of these results is reported here. Spectra from the miniature thermal emission spectrometer and the Panoramic Camera reveal a pyroxene‐rich mineralogy, which is also evident in Mössbauer spectra and in normative mineralogy derived from bulk chemistry measured by the alpha particle X‐ray spectrometer. The correspondence of Bounce Rock’s chemical composition with the composition of certain basaltic shergottites, especially Elephant Moraine (EET) 79001 lithology B and Queen Alexandra Range (QUE) 94201, is very close, with only Cl, Fe, and Ti exhibiting deviations. Chemical analyses further demonstrate characteristics typical of Mars such as the Fe/Mn ratio and P concentrations. Possible shock features support the idea that Bounce Rock was ejected from an impact crater, most likely in the Meridiani Planum region. Bopolu crater, 19.3 km in diameter, located 75 km to the southwest could be the source crater. To date, no other rocks of this composition have been encountered by any of the rovers on Mars. The finding of Bounce Rock by the Opportunity rover provides further direct evidence for an origin of basaltic shergottite meteorites from Mars.  相似文献   

14.
Abstract— Isotopic and trace element compositions of Martian meteorites show that early differentiation of Mars produced complementary crustal and mantle reservoirs that were sampled by later magmatic events. This paper describes a mass balance model that estimates the rare earth element (REE) content and thickness of the crust of Mars from the compositions of shergottites. The diverse REE and Nd isotopic compositions of shergottites are most easily explained by variable addition of light rare earth element (LREE)–enriched crust to basaltic magmas derived from LREE-depleted mantle source regions. Antarctic shergottites EET 79001, ALH 77005, LEW 88516, and QUE 94201 all have strongly LREE-depleted patterns and positive initial 143Nd isotopic compositions, which is consistent with the generation of these magmas from depleted mantle sources and little or no interaction with enriched crust. In contrast, Shergotty and Zagami have negative initial 143Nd isotopic compositions and less pronounced depletions of the LREE, which have been explained by incorporation of enriched crustal components into mantle-derived magmas (Jones, 1989; Longhi, 1991; Borg et al., 1997). The mass balance model presented here derives the REE composition of the crustal component in Shergotty by assuming it represents a mixture between a mantle-derived magma similar in composition to EET 79001A and a LREE-enriched crustal component. The amount of crust in Shergotty is constrained by mixing relations based on Nd-isotopic compositions, which allows the REE pattern of the crustal component to be calculated by mass balance. The effectiveness of this model is demonstrated by the successful recovery of important characteristics of the Earth's continental crust from terrestrial Columbia River basalts. Self-consistent results for Nd-isotopic compositions and REE abundances are obtained if Shergotty contains ～10–30% of LREE-enriched crust with >10 ppm Nd. This crustal component would have moderately enriched LREE (Sm/Nd = 0.25–0.27; 147Sm/144Nd = 0.15–0.17; La/Yb = 2.7–3.8), relatively unfractionated heavy rare earth elements (HREE), and no Eu anomaly. Crust with these characteristics can be produced from a primitive lherzolitic Martian mantle by modest amounts (2–8%) of partial melting, and it would have a globally averaged thickness of <45 km, which is consistent with geophysical estimates. Mars may serve as a laboratory to investigate planetary differentiation by extraction of a primary basaltic crust.  相似文献   

15.
Tissint, a new unaltered piece of Martian volcanic materials, is the most silica‐poor and Mg‐Fe‐rich igneous rock among the “depleted” olivine‐phyric shergottites. Fe‐Mg zoning of olivine suggests equilibrium growth (<0.1 °C h?1) in the range of Fo80–56 and olivine overgrowth (Fo55–18) through a process of rapid disequilibrium (~1.0–5.0 °C h?1). The spatially extended (up to 600 μm) flat‐top Fe‐Mg profiles of olivine indicates that the early‐stage cooling rate of Tissint was slower than the other shergottites. The chemically metastable outer rim of olivine (55) consists of oscillatory phosphorus zoning at the impact‐induced melt domains and grew rapidly compared to the early to intermediate‐stage crystallization of the Tissint bulk. High‐Ca pyroxene to low‐Ca pyroxene and high‐Ca pyroxene to plagioclase ratios of Tissint are more comparable to the enriched basaltic and enriched olivine‐phyric shergottites. Dominance of augite over plagioclase induced augite to control the Ca‐buffer in the residual melt suppressing the plagioclase crystallization, which also caused a profound effect on the Al‐content in the late‐crystallized pyroxenes. Mineral chemical stability, phase‐assemblage saturation, and pressure–temperature path of evolution indicates that the parent magma entered the solidus and left the liquidus field at a depth of 40–80 km in the upper mantle. Petrogenesis of Tissint appears to be similar to LAR 06319, an enriched olivine‐phyric shergottite, during the early to intermediate stage of crystallization. A severe shock‐induced deformation resulted in remelting (10–15 vol%), recrystallization (most Fe‐rich phases), and exhumation of Tissint in a time scale of 1–8 yr. Tissint possesses some distinct characteristics, e.g., impact‐induced melting and deformation, forming phosphorus‐rich recrystallization rims of olivine, and shock‐induced melt domains without relative enrichment of LREEs compared to the bulk; and shared characteristics, e.g., modal composition and magmatic evolution with the enriched basaltic shergottites, evidently reflecting unique mantle source in comparison to the clan of the depleted members.  相似文献   

16.
Northwest Africa (NWA) 8657 is an incompatible trace element-enriched, low-Al basaltic shergottite, similar in texture and chemistry to Shergotty, Zagami, and NWA 5298. It is composed of zoned pyroxene, maskelynite, merrillite, and Ti-oxide minerals with minor apatite, silica, and pyrrhotite. Pyroxene grains are characterized by patchy zoning, with pigeonite or augite cores zoned to Fe-rich pigeonite mantles. The cores have rounded morphologies and irregular margins. Combined with the low Ti/Al of the cores, the morphology and chemistry of the pyroxene grains are consistent with initial crystallization at depth (30–70 km) followed by partial resorption en route to the surface. Enriched rare earth element (REE) equilibrium melt compositions and calculated oxygen fugacities (fO2) conditions for pigeonite cores indicate that the original parent melts were enriched shergottite magmas that staged in chambers at depth within the Martian crust. NWA 8657 does not represent a liquid but rather entrained a proportion of pyroxene crystals from magma chambers where fractional crystallization was occurring at depth. Variation between fO2 and bulk-rock (La/Yb)N of the enriched and intermediate shergottites suggests that oxidation conditions and degree of incompatible element enrichment in the source may not be correlated, as thought previously. Shock melt pockets are characterized by an absence of phosphates and oxide minerals. It is likely that these phases were melted during shock. REEs were redistributed during this process into maskelynite and to a lesser extent the shock melt; however, the overall normalized REE profile of the shock melt is like that of the bulk-rock, but at lower absolute concentrations. Overall, shock melting has had a significant effect on the mineralogy of NWA 8657, especially the distribution of phosphates, which may be significant for geochronological applications of this meteorite and other Martian meteorites with extensive shock melt.  相似文献   

17.
Abstract— Queen Alexandra Range (QUE) 94281, a lunar meteorite recently discovered in Antarctica, is a glassy-matrix, clast-rich regolith breccia containing a mixture of mafic, volcanic-glass and gabbroic constituents and a diverse set of highland constituents. In thin section, the clast assemblage is dominated by coarse mineral debris from a shallow intrusive or hypabyssal setting, or from deep within a thick mare flow. Abundant coarse-grained pyroxene clasts have fine-scale exsolution lamellae and compositions similar to pyroxenes of known lunar very-low-Ti (VLT) basalts and other lunar meteorites of basaltic composition. Pyroxene compositions follow Fe-enrichment extending to hedenbergite, which is associated with fayalite and cristobalite, indicating slow cooling. We refer to the protolith of the crystalline VLT component as VLT gabbro. Fragments of pyroclastic glasses that have high Fe and low Ti concentrations, similar to the pyroclastic green glasses known from Apollo samples, are common. Lithic clasts include abundant subrounded, glassy to cryptocrystalline, aluminous (～17–30 wt% Al2O3) KREEP-poor melt breccias of highland origin and a variety of other feldspathic impactites. On the basis of composition of our subsamples, QUE 94281 consists of ～54 wt% mafic or “mare” components and 46 wt% feldspathic or “highland” components. The bulk composition of QUE 94281 is similar to that of Yamato (Y) 793274, but QUE 94281 has slightly greater concentrations of some siderophile elements and slightly lower concentrations of those elements contributed mainly by mafic constituents. Differences in siderophile element concentrations are consistent with longer surface exposure of QUE 94281. Minor differences in trace element variations of subsamples of the two meteorites suggest subtle differences in the composition of their highland constituents. Nonetheless, the overall similarity of compositions supports the possibility that they were ejected from the same source region on the Moon. The crystalline VLT component of QUE 94281 differs from those known from Apollo 17 and Luna 24 VLT lithologies and from that of basaltic breccia Elephant Moraine (EET) 87521. The VLT-gabbro component and the ferroan VLT volcanic glasses in QUE 94281 have compositions that may be petrogenetically related by derivation from a common picritic parent composition, represented by an ultramafic glass found in QUE 94281.  相似文献   

18.
Accurate computational modeling allows the use of software as a first approach to some petrological problems that typically require experimentation, but most programs have not yet been fully tested for accuracy with lunar or Martian melt compositions. The programs pMELTS, MAGPOX, and Perple_X stand out for phase equilibrium modeling, as their calibrations include experiments of lunar compositions or have precise thermodynamic constraints for similar compositions. A set of lunar mare basalts, picritic glasses, and basaltic Martian compositions with known experimentally determined multiple saturation point (MSP) conditions were used here for phase equilibrium modeling. The accuracy of each program was tested through the determination of MSPs on the liquidus of the selected compositions. This point in pressure–temperature space can be considered as a direct proxy of the stable phases and the equilibrium conditions during partial melting of mantle sources. We identify a trend in experimental data between MSP temperature and MgO, CaO, and SiO2 concentrations, and similar trends are found in model results. However, only Perple_X is able to closely match the experimental data, despite the fact it does not accurately model ilmenite saturation for high-Ti lunar basalts. We find that pMELTS miscalculates olivine saturation for MgO-rich compositions and MAGPOX systematically underestimates MSP pressure and temperatures and can only be used when olivine is the liquidus phase. For modeling lunar or Martian basalt compositions, Perple_X can be used for optimal results, although no software is yet capable of bypassing the need to constrain MSP conditions through experimentation.  相似文献   

19.
Abstract— Elephant Moraine (EET) A79001 is the only Martian meteorite that consists of both an olivine‐phyric shergottite (lithology A) and a basaltic shergottite (lithology B). The presence of these lithologies in one rock has previously been ascribed to mixing processes (either magmatic or impact‐induced). Here we present data regarding phase changes across the contact between the lithologies. These data show that the contact is gradational and suggest that it is a primary igneous feature consistent with crystallization of a single cooling magma. We present a model to establish a petrogenetic connection between an olivine‐phyric and a basaltic shergottite through differentiation. The model involves the shallow or surface emplacement of a magma that contained pre‐eruptive solids (phenocrysts and minor xenocrysts). Subsequent differentiation via crystal settling and in situ crystallization (Langmuir 1989) resulted in a layered sequence of lithology A overlain by lithology B, with gradations in modal abundance of maskelynite (increasing from A to B) and pigeonite/maskelynite (decreasing from A to B), and a gradational change in pattern of pyroxene zonation (zones of magnesian augite separating magnesian and ferroan pigeonite appear and thicken into B) across the contact. A pigeonite phenocryst‐bearing zone near the contact in lithology B appears to be intermediate between lithology A and the bulk of lithology B (which resembles basaltic shergottite Queen Alexandra Range [QUE] 94201). Re‐examination of Sr isotopic compositions in lithology A and across the contact is required to test and constrain the model.  相似文献   

20.
The Martian meteorites record a wide diversity of environments, processes, and ages. Much work has been done to decipher potential mantle sources for Martian magmas and their interactions with crustal and surface environments. Chlorine isotopes provide a unique opportunity to assess interactions between Martian mantle‐derived magmas and the crust. We have measured the Cl‐isotopic composition of 17 samples that span the range of known ages, Martian environments, and mantle reservoirs. The 37Cl of the Martian mantle, as represented by the olivine‐phyric shergottites, NWA 2737 (chassignite), and Shergotty (basaltic shergottite), has a low value of approximately ?3.8‰. This value is lower than that of all other planetary bodies measured thus far. The Martian crust, as represented by regolith breccia NWA 7034, is variably enriched in the heavy isotope of Cl. This enrichment is reflective of preferential loss of 35Cl to space. Most basaltic shergottites (less Shergotty), nakhlites, Chassigny, and Allan Hills 84001 lie on a continuum between the Martian mantle and crust. This intermediate range is explained by mechanical mixing through impact, fluid interaction, and assimilation‐fractional crystallization.  相似文献   

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