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1.
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2.
Abstract— We report a high‐resolution 40Ar‐39Ar study of mineral separates and whole‐rock samples of olivine‐phyric (Dhofar 019, Sayh al Uhaymir [SaU] 005) and basaltic (Shergotty, Zagami) shergottites. Excess argon is present in all samples. The highest (40Ar/36Ar)trapped ratios are found for argon in pyroxene melt inclusions (?1500), maskelynite (?1200), impact glass (?1800) of Shergotty and impact glass of SaU 005 (?1200). A high (40Ar/36Ar)trapped component‐usually uniquely ascribed to Martian atmosphere‐can also originate from the Martian interior, indicating a heterogeneous Martian mantle composition. As additional explanation of variable high (40Ar/36Ar)trapped ratios in shocked shergottites, we suggest argon implantation from a “transient atmosphere” during impact induced degassing. The best 40Ar‐39Ar age estimate for Dhofar 019 is 642 ± 72 Ma (maskelynite). SaU 005 samples are between 700–900 Ma old. Relatively high 40Ar‐39Ar ages of melt inclusions within Dhofar 019 (1086 ± 252 Ma) and SaU 005 olivine (885 ± 66 Ma) could date entrapment of a magmatic liquid during early olivine crystallization, or reflect unrecognized excess 40Ar components. The youngest 40Ar‐39Ar age of Shergotty separates (maskelynite) is ?370 Ma, that of Zagami is ?200 Ma. The 40Ar‐39Ar chronology of Dhofar 019 and SaU 005 indicate >1 Ga ages. Apparent ages uncorrected for trapped (e.g., Martian atmosphere, mantle) argon components approach 4.5 Ga, but are not caused by inherited 40Ar, because excess 40Ar is supported by 36Artrapped. Young ages obtained by 40Ar‐39Ar and other chronometers argue for primary rather than secondary events. The cosmic ray exposure ages calculated from cosmogenic argon are 15.7 ± 0.7 Ma (Dhofar 019), 1.0–1.6 Ma (SaU 005), 2.1–2.5 Ma (Shergotty) and 2.2–3.0 Ma (Zagami).  相似文献   

3.
Abstract— We report on the discovery of a new shergottite from South Morocco. This single stone weighing 320 g is referenced as Northwest Africa (NWA) 856 with Djel Ibone as a synonymous name. It is a fresh, fine‐grained basaltic rock consisting mainly of two pyroxenes (total ?68 vol%: 45% pigeonite, En61‐16Wo9–22Fs26–68; 23% augite, En46‐26Wo34‐29Fs21–43) and plagioclase converted to maskelynite (?23 vol%, Ab43–57Or1–5An54‐36). Accessory minerals include merrillite, Cl‐apatite, pyrrhotite, ilmenite, ulvöspinel, silica (stishovite and glass), amorphous K‐feldspar and baddeleyite. Amorphous mixtures of maskelynite and silica occur most commonly as median layers inside maskelynite laths. In addition, melt pockets (?2 vol%) were recognized with relics of maskelynite, pyroxene and both dense silica glass and stishovite occurring as both grains and submicrometer needles. The compositions of the melt pockets are consistent with mixtures of maskelynite and pyroxenes with an average of ?50 vol% maskelynite. The meteorite is highly fractured at all scales. The bulk composition of NWA 856 has been measured for 44 elements. It is an Al‐poor ferroan basaltic rock which strongly resembles Shergotty and Zagami in its major and trace element composition. The nearly flat rare earth element (REE) pattern (La/Lu)n = 0.9, is similar to that of Shergotty or Zagami and differs significantly from NWA 480, another Moroccan shergottite recently described. According to the U, Ba and Sr abundances, NWA 856 is not significantly weathered. The oxygen isotopes (δ18O = +5.03%, δ17O = +3.09%, and Δ17O = +0.47%) are in agreement with the martian origin of this meteorite. On the basis of grain size, pyroxene zoning and composition, abundance of silica inclusions associated with maskelynite, trace element abundances, REE pattern and oxygen isotopes, pairing with NWA 480 is excluded. The similarity with Shergotty and Zagami is striking. The only significant differences are a larger grain size, a greater abundance of silica and melt pockets, a slightly more restricted range of pyroxene compositions and the absence of significant mesostasis.  相似文献   

4.
Abstract— An experimental investigation of the Shergotty meteorite was performed at 0.1 MPa under anhydrous conditions at the quartz‐fayalite‐magnetite buffer and at 100 and 200 MPa under H2O‐saturated conditions at the nickel‐nickel oxide buffer. The results of these experiments are used to infer magmatic conditions recorded by co‐crystallization of augite and pigeonite phenocrysts found in Shergotty and to investigate the effect of H2O on fractional crystallization paths followed by shergottite magmas. The phase relations and compositions of the homogeneous magnesian pyroxene cores in Shergotty are most closely approximated by crystallization under H2O‐saturated conditions at 1120 °C (± 10 °C) and 56 MPa (± 18 MPa), corresponding to dissolved H2O contents of 1.8 wt% (± 0.6 wt%) and a depth of 5 km (± 1.5 km) in the martian crust (uncertainties are 2s? values). The Shergotty magma then lost this water during ascent and eruption. Fractional crystallization of the Shergotty magma under anhydrous conditions produces liquids that follow a strong Fe‐enrichment trend at nearly constant SiO2. Crystallization under H2O‐saturated conditions generates derivative liquids, depleted in FeO and Al2O3 and enriched in SiO2, that are compositionally similar to the Mars Pathfinder andesite rock composition. The presence of ～1.8 wt% water in Shergotty parental magmas could result from assimilation of hydrated crustal materials or from dehydration of hydrous phases in the mantle source region.  相似文献   

5.
Abstract— This study provides a complete data set of all five noble gases for bulk samples and mineral separates from three Martian shergottites: Shergotty (bulk, pyroxene, maskelynite), Zagami (bulk, pyroxene, maskelynite), and Elephant Moraine (EET) A79001, lithology A (bulk, pyroxene). We also give a compilation of all noble gas and nitrogen studies performed on these meteorites. Our mean values for cosmic‐ray exposure ages from 3He, 21Ne, and 38Ar are 2.48 Myr for Shergotty, 2.73 Myr for Zagami, and 0.65 Myr for EETA79001 lith. A. Serious loss of radiogenic 4He due to shock is observed. Cosmogenic neon results for bulk samples from 13 Martian meteorites (new data and literature data) are used in addition to the mineral separates of this study in a new approach to explore evidence of solar cosmic‐ray effects. While a contribution of this low‐energy irradiation is strongly indicated for all of the shergottites, spallation Ne in Chassigny, Allan Hills (ALH) 84001, and the nakhlites is fully explained by galactic cosmic‐ray spallation. Implanted Martian atmospheric gases are present in all mineral separates and the thermal release indicates a near‐surface siting. We derive an estimate for the 40Ar/36Ar ratio of the Martian interior component by subtracting from measured Ar in the (K‐poor) pyroxenes the (small) radiogenic component as well as the implanted atmospheric component as indicated from 129Xe, * excesses. Unless compromised by the presence of additional components, a high ratio of ～2000 is indicated for Martian interior argon, similar to that in the Martian atmosphere. Since much lower ratios have been inferred for Chassigny and ALH 84001, the result may indicate spatial and/or temporal variations of 40Ar/36Ar in the Martian mantle.  相似文献   

6.
Amphibole in chassignite melt inclusions provides valuable information about the volatile content of the original interstitial magma, but also shock and postshock processes. We have analyzed amphibole and other phases from NWA 2737 melt inclusions, and we evaluate these data along with published values to constrain the crystallization Cl and H2O content of phases in chassignite melt inclusions and the effects of shock on these amphibole grains. Using a model for the Cl/OH exchange between amphibole and melt, we estimate primary crystallization OH contents of chassignite amphiboles. SIMS analysis shows that amphibole from NWA 2737 currently has 0.15 wt% H2O. It has lost ~0.6 wt% H2O from an initial 0.7–0.8 wt% H2O due to intense shock. Chassigny amphibole had on average 0.3–0.4 wt% H2O and suffered little net loss of H2O due to shock. NWA 2737 amphibole has δD ≈ +3700‰; it absorbed Martian atmosphere‐derived heavy H in the aftermath of shock. Chassigny amphibole, with δD ≤ +1900‰, incorporated less heavy H. Low H2O/Cl ratios are inferred for the primitive chassignite magma, which had significant effects on melting and crystallization. Volatiles released by the degassing of Martian magma were more Cl‐rich than on Earth, resulting in the high Cl content of Martian surface materials.  相似文献   

7.
Abstract— We studied micro Raman spectroscopy of amphiboles and pyroxenes in the martian meteorites Zagami and Lewis Cliff (LEW) 88516. The obtained Raman spectra of the amphiboles are similar to those of kaersutite, reconfirming the previous studies that they are kaersutitic amphiboles enriched in Ca, Al, and Ti. Even though actinolite belongs to the same amphibole group (calcic amphibole) as kaersutite, the Raman spectra of terrestrial actinolite are distinct from those of kaersutite, probably reflecting complex amphibole crystal structures. The Al‐Ti‐rich pyroxene observed in the magmatic inclusions within LEW 88516 olivine is compositionally similar to kaersutite but shows Raman spectra nearly identical to the regular pyroxene rather than amphibole. In contrast to amphibole, this will be due to relatively simple crystal structures of pyroxene. Thus, the Raman spectra of Al‐Ti‐rich phases in the martian meteorites are distinct between kaersutite and Al‐Ti‐rich pyroxene, and this study demonstrates that micro Raman spectroscopy is one of the best tools to perform mineralogical characterization of mineral phases in martian meteorites.  相似文献   

8.
The unusual achondrite Shergotty resembles terrestrial diabases, and textural and chemical evidence indicates pre-settling and post-settling crystallization of zoned augite (En48Fs19Wo33-En25Fs47Wo28) and pigeonite (En61Fs26Wo13-En21Fs61Wo18) coupled with late crystallization of plagioclase (Ab43An56/Or1-Ab56An41Or3: now shocked to maskelynite), titanomagnetite-ilmenite composite grains, mesostasis (normative Qz34Ab21An5Or38Fs2, assuming Fe as ferrous), whitlockite, pyrrhotite (Fe0.94S), fayalite (Fo10), baddeleyite and chlorapatite. The oxide compositions (Usp62Mt38, Al2O3 2.4, Cr2O3 0.8 wt %; Ilm95Hm5) indicate ～ 850 °C and log oxygen fugacity ? 14, while the occurrence of fayalite rims on mesostasis next to ilmenite indicates 890 °C. Bearing in mind experimental uncertainties, these data are consistent with late-stage crystallization under relatively high oxygen fugacity, as indicated by coexistence of fayalite, Ti-magnetite and a silica glass. The high alkali content of the maskelynite and mesostasis, coupled with the redox state, indicates that the Shergotty meteorite resembles terrestrial basalts more than any other meteorites. Nevertheless the absence of H2O, as shown by the occurrence of phosphorus in whitlockite rather than in hydroxylapatite, distinguish the Shergotty achondrite from typical terrestrial diabases. Whereas the FeO/MnO ratios of pyroxenes from the Moon, Earth and several differentiated meteorites are independent of FeO, the ratio for Shergotty pyroxenes changes from 30 to 40 with increasing FeO, and the linear trend extrapolates to 0.2 MnO for zero iron. Hence caution is needed in using FeO/MnO as a planetary indicator. For pyroxenes, Na is almost independent of Fe/Mg while Ti increases and Cr decreases with increasing Fe/Mg. Maskelynite contains 0.5–0.25 wt % K2O, 0.6 wt % FeO, 0.04 TiO2, 0.04–0.07 MgO, ～ 0.01 BaO and 0.02–0.03 P2O5. A bulk analysis calculated from the mode and compositions of the minerals matches quite well with two bulk chemical analyses but not with a third.  相似文献   

9.
Several controversies are associated with the age and origin of the shergottite meteorites, a suite of basaltic samples from Mars. Here, it will be argued that (1) the shergottites have a young igneous age, ≤600 Myr, (2) their parent magmas were relatively dry, (3) the range of initial isotopic compositions in shergottites is most likely due to assimilation of crustal materials by mantle‐derived basaltic magmas, and (4) the intercumulus liquid compositions of shergottites such as Shergotty and Zagami are relatively well constrained.  相似文献   

10.
Abstract— Samples from a suite of Shergotty—Nakhla—Chassigny (SNC) meteorites were analyzed for their O isotopic ratios by a modified version of the laser fluorination technique. Measured isotopic ratios (17O/16O and 18O/16O) from bulk samples of the Shergottites, EETA79001, Shergotty and Zagami; the Nakhlite Lafayette; and Chassigny are similar to those reported in the literature, as are those from olivine and pyroxene mineral separates from Lafayette. Iddingsite, a preterrestrial alteration product of Lafayette, was measured for the first time as a separate phase. Oxygen isotopic ratios increase with the percentage of iddingsite in a sample to a maximum δ18O of 14.4% for a ～90% separate. Based on these measurements, end-member iddingsite has a δ18O of 15.6%, which places it among other 18O-enriched secondary phases (carbonate and silica) observed in SNC meteorites. The relatively large difference in δ18O between iddingsite and the olivine and pyroxene it replaces (～11%) is typical of low-temperature alteration products. A range of crustal fluid δ18O values can be interpreted from the δ18O for end-member iddingsite, assuming isotopic equilibrium was achieved during low-temperature hydrous alteration (<100 °C; Treiman et al., 1993). The calculated range of values, ?15 to 5%, depends on many factors including: (1) the modal mineralogy of iddingsite, (2) potential isotopic exchange among other O-bearing phases such as host silicate and carbonate, and (3) exchange with evolved or exotic O reservoirs on Mars. Despite the lack of constraints, the calculated range is consistent with isotopic exchange, and possibly equilibria, among components of the CO2-carbonate-iddingsite-H2O system at low temperature. The SNC meteorite samples in this study have Δ17O values that are indistinguishable from bulk Mars (0.30%), except for a single, small sample of iddingsite that has an anomalous Δ17O of ～1.4%. While analytical difficulties make isotopic measurements for this sample problematic, the Δ17O is similar in direction to Δ17O reported for waters extracted from bulk samples of Lafayette (Karlsson et al., 1992). If the Δ17O for iddingsite is confirmed, it can be concluded that evolved or exotic fluids on Mars have contributed volatiles to the O reservoir from which iddingsite formed 130 to 700 Ma ago.  相似文献   

11.
Abstract— We report the elemental and isotopic composition of the noble gases as well as the chemical abundances in pyroxene, maskelynite/mesostasis glass, and bulk material of Shergotty and of bulk samples from Chassigny and Yamato 793605. The 40K-40Ar isochron for the Shergotty minerals yields a gas retention age of 196 Ma, which is, within errors, in agreement with previously determined Rb-Sr internal isochron ages. Argon that was trapped at this time has a 40Ar/36Ar ratio of 1100. For Chassigny and Y-793605, we obtain trapped 40Ar/36Ar ratios of 1380 and 950, respectively. Using these results and literature data, we show that the three shergottites, Shergotty, Zagami, and QUE 94001; the lherzolites ALH 77005, LEW 88516, and Y-793605; as well as Chassigny and ALH 84001 contain a mixture of Martian mantle and atmospheric Ar; whereas, the trapped 40Ar/36Ar ratio of the nakhlites, Nakhla, Lafayette, and Governador Valadares cannot be determined with the present data. We show that Martian atmospheric trapped Ar in Martian meteorites is correlated with the shock pressure that they experienced. Hence, we conclude that the Martian atmospheric gases were introduced by shock into the meteoritic material. For the Shergotty minerals, we obtain 3He-, 21Ne-, and 38Ar-based cosmic-ray exposure ages of 3.0 Ma, and for the lherzolite Y-793605, 4.0 Ma, which confirms our earlier conclusion that the lherzolites were ejected from Mars ～1 Ma before the shergottites. Chassigny yields the previously known ejection age of 11.6 Ma.  相似文献   

12.
Abstract— Isotopic signatures and concentrations of xenon have been measured in Shergotty mineral separates by laser step heating. Martian atmosphere and ‘martian interior’ xenon are present, as is a spallation component. Martian atmospheric xenon is 5–10 times more concentrated in opaque minerals (magnetite, ilmenite, and pyrrhotite) and maskelynite than in pyroxenes, perhaps reflecting grain size variation. This is shown to be consistent with shock incorporation. A component consisting of solar xenon with a fission contribution, similar to components previously identified in martian meteorites and associated with the martian interior, is best defined in the pyroxene‐dominated separates. This component exhibits a consistent 129Xe (129Xe/132Xe ?1.2) excess over solar/planetary (129Xe/132Xe ?1.04). We suggest that gas present in the melt, perhaps a mixture of interior xenon and martian atmosphere, was incorporated into the pyroxenes in Shergotty as the minerals crystallized.  相似文献   

13.
Abstract— MacAlpine Hills (MAC) 87300 and 88107 are two unusual carbonaceous chondrites that are intermediate in chemical composition between the CO3 and CM2 meteorite groups. Calcium‐aluminum‐rich inclusions (CAIs) from these two meteorites are mostly spinel‐pyroxene and melilite‐rich (Type A) varieties. Spinel‐pyroxene inclusions have either a banded or nodular texture, with aluminous diopside rimming Fe‐poor spinel. Melilite‐rich inclusions (Åk4–42) are irregular in shape and contain minor spinel (FeO <1 wt%), perovskite and, more rarely, hibonite. The CAIs in MAC 88107 and 87300 are similar in primary mineralogy to CAIs from low petrologic grade CO3 meteorites but differ in that they commonly contain phyllosilicates. The two meteorites also differ somewhat from each other: melilite is more abundant and slightly more Al‐rich in inclusions from MAC 88107 than in those from MAC 87300, and phyllosilicate is more abundant and Mg‐poor in MAC 87300 CAIs relative to that in MAC 88107. These differences suggest that the two meteorites are not paired. The CAI sizes and the abundance of melilite‐rich CAIs in MAC 88107 and 87300 suggests a genetic relationship to CO3 meteorites, but the CAIs in both have suffered a greater degree of aqueous alteration than is observed in CO meteorites. Aluminum‐rich melilite in CAIs from both meteorites generally contains excess 26Mg, presumably from the in situ decay of 26Al. Although well‐defined isochrons are not observed, the 26Mg excesses are consistent with initial 26Al/27Al ratios of approximately 3–5 times 10?5. An unusual hibonite‐bearing inclusion is isotopically heterogeneous, with two large and abutting hibonite crystals showing significant differences in their degrees of mass‐dependent fractionation of 25Mg/24Mg. The two crystals also show differences in their inferred initial 26Al/27Al ratios, 1 × 10?5 vs. ≤3 × 10?6.  相似文献   

14.
Abstract— Approximately 275 mineral species have been identified in meteorites, reflecting diverse redox environments, and, in some cases, unusual nebular formation conditions. Anhydrous ordinary, carbonaceous and R chondrites contain major olivine, pyroxene and plagioclase; major opaque phases include metallic Fe-Ni, troilite and chromite. Primitive achondrites are mineralogically similar. The highly reduced enstatite chondrites and achondrites contain major enstatite, plagioclase, free silica and kamacite as well as nitrides, a silicide and Ca-, Mg-, Mn-, Na-, Cr-, K- and Ti-rich sulfides. Aqueously altered carbonaceous chondrites contain major amounts of hydrous phyllosilicates, complex organic compounds, magnetite, various sulfates and sulfides, and carbonates. In addition to kamacite and taenite, iron meteorites contain carbides, elemental C, nitrides, phosphates, phosphides, chromite and sulfides. Silicate inclusions in IAB/IIICD and IIE iron meteorites consist of mafic silicates, plagioclase and various sulfides, oxides and phosphates. Eucrites, howardites and diogenites have basaltic to orthopyroxenitic compositions and consist of major pyroxene and calcic plagioclase and several accessory oxides. Ureilites are made up mainly of calcic, chromian olivine and low-Ca clinopyroxene embedded in a carbonaceous matrix; accessory phases include the C polymorphs graphite, diamond, lonsdaleite and chaoite as well as metallic Fe-Ni, troilite and halides. Angrites are achondrites rich in fassaitic pyroxene (i.e., Al-Ti diopside); minor olivine with included magnesian kirschsteinite is also present. Martian meteorites comprise basalts, lherzolites, a dunite and an orthopyroxenite. Major phases include various pyroxenes and olivine; minor to accessory phases include various sulfides, magnetite, chromite and Ca-phosphates. Lunar meteorites comprise mare basalts with major augite and calcic plagioclase and anorthositic breccias with major calcic plagioclase. Several meteoritic phases were formed by shock metamorphism. Martensite (α2-Fe,Ni) has a distorted body-centered-cubic structure and formed by a shear transformation from taenite during shock reheating and rapid cooling. The C polymorphs diamond, lonsdaleite and chaoite formed by shock from graphite. Suessite formed in the North Haig ureilite by reduction of Fe and Si (possibly from olivine) via reaction with carbonaceous matrix material. Ringwoodite, the spinel form of (Mg,Fe)2SiO4, and majorite, a polymorph of (Mg,Fe)SiO3 with the garnet structure, formed inside shock veins in highly shocked ordinary chondrites. Secondary minerals in meteorite finds that formed during terrestrial weathering include oxides and hydroxides formed directly from metallic Fe-Ni by oxidation, phosphates formed by the alteration of schreibersite, and sulfates formed by alteration of troilite.  相似文献   

15.
Abstract— In a study of the isotopic signatures of trapped Xe in shock-produced glass of shergottites and in ALH 84001, we observe three components: (1) modern Martian atmospheric Xe that is isotopically mass fractionated relative to solar Xe, favoring the heavy isotopes, (2) solar-like Xe, as previously observed in Chassigny, and (3) an isotopically fractionated (possibly ancient) component with little or no radiogenic 129Xerad. In situ-produced fission and spallation components are observed predominantly in the high-temperature steps. Heavy N signatures in ALH 84001, EET 79001 and Zagami reveal Martian atmospheric components. The low-temperature release of ALH 84001 shows evidence for the presence of a light N component (δ15N ≤ -21%), which is consistent with the component observed in the other Shergotty, Nakhla and Chassigny (SNC) group meteorites. The highest observed 129Xe/130Xe ratio of 15.60 in Zagami and EET 79001 is used here to represent the present Martian atmospheric component, and the isotopic composition of this component is compared with other solar system Xe signatures. The 129Xe/130Xe ratios in ALH 84001 are lower but appear to reflect varying mixing ratios with other components. The consistently high 129Xe/130Xe ratios in rocks of different radiometric ages suggest that Martian atmospheric Xe evolved early on. As already concluded in earlier work, only a small fission component is observed in the Martian atmospheric component. Assuming that a chondritic 244Pu/129I initial ratio applies to Mars, this implies that either Pu-derived fission Xe is retained in the solid planet (in fact, in situ-produced fission Xe is observed in ALH 84001) or may reflect a very particular degassing history of the planet.  相似文献   

16.
Abstract— Cosmic‐ray exposure (CRE) ages and Mars ejection times were calculated from the radionuclide 81Kr and stable Kr isotopes for seven martian meteorites. The following 81Kr‐Kr CRE ages were obtained: Los Angeles = 3.35 ± 0.70 Ma; Queen Alexandra Range 94201 = 2.22 ± 0.35 Ma; Shergotty = 3.05 ± 0.50 Ma; Zagami = 2.98 ± 0.30 Ma; Nakhla = 10.8 ± 0.8 Ma; Chassigny = 10.6 ± 2.0 Ma; and Allan Hills 84001 = 15.4 ± 5.0 Ma. Comparison of these ages with previously obtained CRE ages from the stable noble gas nuclei 3He, 21Ne, and 38Ar shows excellent agreement. This indicates that the method for the production rate calculation for the stable nuclei is reliable. In all martian meteorites we observe effects induced by secondary cosmic‐ray produced epithermal neutrons. Epithermal neutron fluxes, φn (30–300 eV), are calculated based on the reaction 79Br(n, γβ)80Kr. We show that the neutron capture effects were induced in free space during Mars‐Earth transfer of the meteoroids and that they are not due to a pre‐exposure on Mars before ejection of the meteoritic material. Neutron fluxes and slowing down densities experienced by the meteoroids are calculated and pre‐atmospheric sizes are estimated. We obtain minimum radii in the range of 22–25 cm and minimum masses of 150–220 kg. These results are in good agreement with the mean sizes reported for model calculations using current semiempirical data.  相似文献   

17.
Northwest Africa (NWA) 10414 is an unusual shergottite with a cumulate texture. It contains 73% coarse prismatic pigeonite, plus 18% interstitial maskelynite, 2% Si‐rich mesostasis, 2% merrillite, and minor chromite‐ulvöspinel. It contains no olivine, and only ~3% augite. Phase compositions are pigeonite (En68‐43Fs27‐48Wo5‐15) and maskelynite An~54‐36, more sodic than most maskelynite in shergottites. Chromite‐ulvöspinel composition plots between the earliest and most fractionated spinel‐group minerals in olivine‐phyric shergottites. NWA 10414 mineralogically resembles the contact facies between Elephant Moraine 79001 lithologic units A and B, with abundant pigeonite phenocrysts, though it is coarser grained. Its most Mg‐rich pigeonite also has a similar composition to the earliest crystallized pyroxenes in several other shergottites, including Shergotty. The Shergotty intercumulus liquid composition crystallizes pigeonite with a similar composition range to NWA 10414 pigeonite, using PETROLOG. Olivine‐phyric shergottite NWA 6234, with a pure magma composition, produces an even better match to this pigeonite composition range, after olivine crystallization. These observations suggest that after the accumulation of olivine from an olivine‐phyric shergottite magma, the daughter liquid could precipitate pigeonite locally to form this pigeonite cumulate, before the crystallization of overlying liquid as a normal basaltic shergottite.  相似文献   

18.
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   

19.
Angrite meteorites are samples of early planetesimal magmatic rocks, distinguished from more typical “basaltic eucrites” by compositions that are silica undersaturated, relatively oxidized, and with high CaO/Al2O3. The latter is not expected from nebular, chondritic materials that might form a primitive mantle, such as a source enriched in refractory inclusions with fixed CaO/Al2O3 (e.g., CV chondrite). Here we present results of “reversal” crystallization experiments for two possible parental angrite compositions (approximating the D'Orbigny meteorite) to investigate the role of spinel as a sink for Al2O3. This mineral has previously been produced with angritic melts during “forward” melting of CV chondrite and may be abundant in the angrite source. At oxidizing conditions, we confirm that spinel is a liquidus phase and that angritic magmas form near the olivine-anorthite-spinel-liquid peritectic. A stability gap separates Al-rich liquidus spinels and lower temperature spinels, the latter of which are similar to those in basaltic eucrites. Al-rich spinel is likely more abundant in the angritic source than other Fe-rich core-forming components such as metal or sulfide, and a CV chondrite-like composition generates most features of angrite magmas by fractionation of observed olivine and liquidus spinel. Direct CaO excess, via carbonate addition, is therefore limited. In this model, discrepancies remain for Li, Sc, Cr(-Al), and Ba, which may record local accretion conditions or early processing. The possible role of spinel as a sink for 26Al may have strong influence on the thermal evolution of the angrite parent body.  相似文献   

20.
Abstract— Vacuum pyrolysis and quadrupole mass spectrometry were used to measure evolved-gas profiles and total concentrations of H2O, CO2, CO, SO2, S2, H2S, HCl, Cl, and hydrocarbons in both exterior and interior samples of shergottites (ALHA77005, EETA79001, and Shergotty), a nakhlite (Nakhla), and eucrites (ALHA81001, EETA79004, and Pasamonte). Eucrites were analyzed as control samples to monitor effects of terrestrial weathering and contamination, relative to properties sought for the shergottite-nakhlite parent body. In contrast with eucrites, shergottites and Nakhla contain large proportions of their sulfur as oxidized sulfur compounds. Sulfate occurs in all shergottite and Nakhla samples and carbonate was confirmed in EETA79001 and Nakhla. Carbonate and sulfate abundances are inversely correlated but total chlorine abundance varies directly with fractional sulfate abundance. Most of the volatile compounds seem to be anhydrous, based on low bulk water contents in the meteorites (<0.1% H2O), although Nakhla might contain significant water that is chemically associated with chlorine. Traces of saturated and unsaturated hydrocarbons in some samples are most likely terrestrial contaminants. The indigenous volatile compounds indicate that the shergottite-nakhlite parent body was highly oxidizing and supported aqueous geochemistry during at least part of its history.  相似文献   

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