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1.
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   

2.
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   

3.
Abstract— Basaltic shergottites display a systematic decrease in K/Th, K/U, and K/La ratios with increasing K content. These trends are interpreted as mixing lines between relatively young martian magmas derived from highly depleted mantle sources and an ancient large‐ion lithophile (LIL) element‐enriched crustal component. One implication of this is that a substantial fractionation of these ratios occurs during the early crustal differentiation on Mars. Isotopic evidence from SNC meteorites and compositional data from Pathfinder and orbital gamma ray spectroscopy suggest that in excess of 50% of the LIL element complement of Mars resides in the crustal reservoir. If so, the primitive mantle of Mars is significantly more volatile‐depleted (i.e., lower K/Th, K/U, K/La) than previously thought but probably (though not necessarily) still less volatile‐depleted than the primitive mantle of the Earth. The La/Th ratios of virtually all SNC meteorites are subchondritic, including those with the most severe LREE‐depletion. Extrapolation of the basaltic shergottite trend suggests that both the depleted mantle end member and the enriched crustal end member have subchondritic La/Th ratios. This is in contrast with the Earth where basalts from LIL element‐depleted sources such as MORB have superchondritic La/Th ratios, complementary to the subchondritic ratios of the continental crust. Accordingly, assuming that the refractory elements are in chondritic proportions for the Mars primitive mantle, an additional major geochemical reservoir must exist on Mars that may not yet have been sampled.  相似文献   

4.
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   

5.
Abstract— The newly found meteorite Northwest Africa 6234 (NWA 6234) is an olivine (ol)‐phyric shergottite that is thought, based on texture and mineralogy, to be paired with Martian shergottite meteorites NWA 2990, 5960, and 6710. We report bulk‐rock major‐ and trace‐element abundances (including Li), abundances of highly siderophile elements, Re‐Os isotope systematics, oxygen isotope ratios, and the lithium isotope ratio for NWA 6234. NWA 6234 is classified as a Martian shergottite, based on its oxygen isotope ratios, bulk composition, and bulk element abundance ratios, Fe/Mn, Al/Ti, and Na/Al. The Li concentration and δ7Li value of NWA 6234 are similar to that of basaltic shergottites Zagami and Shergotty. The rare earth element (REE) pattern for NWA 6234 shows a depletion in the light REE (La‐Nd) compared with the heavy REE (Sm‐Lu), but not as extreme as the known “depleted” shergottites. Thus, NWA 6234 is suggested to belong to a new category of shergottite that is geochemically “intermediate” in incompatible elements. The only other basaltic or ol‐phyric shergottite with a similar “intermediate” character is the basaltic shergottite NWA 480. Rhenium‐osmium isotope systematics are consistent with this intermediate character, assuming a crystallization age of 180 Ma. We conclude that NWA 6234 represents an intermediate compositional group between enriched and depleted shergottites and offers new insights into the nature of mantle differentiation and mixing among mantle reservoirs in Mars.  相似文献   

6.
Abstract— The shergottites exhibit a range of major and trace element compositions, crystallization ages, and initial Sr, Nd, Hf, and Pb isotopic compositions. To constrain the physical mechanisms by which shergottites obtain their compositional characteristics, we examined the major and trace element record preserved in olivine in the more primitive shergottites. Based on such characteristics as the Mg#, V zoning, calculated DNi,Co, the olivine in Y‐980459 are most likely phenocrysts. Many of these same characteristics indicate that the olivines in other shergottites are not in equilibrium with the adjacent melt. However, in most cases they are not xenocrystic, but additions of olivine from the same basaltic system. Elephant Moraine (EET) A79001 may be an exception with the olivine data suggesting that it is xenocrystic. In this case, the olivine crystallized from a reduced and LREE‐depleted melt and was incorporated into an oxidized and enriched basalt. Vanadium and CaO in olivine appear to record the appearance of spinel and pyroxene on the liquidus of most of the shergottites. Most of the olivine shergottites represent basalts produced by melting of reduced (IW to IW + 1), depleted mantle sources. Olivine data indicate that many of the primary melts derived from this source had similar Ni, Co, and Mn. Shergottites such as Northwest Africa (NWA) 1110/1068 and perhaps Roberts Massif (RBT) 04261 that appear to be derived from more enriched sources have distinctly different olivine. In the case of NWA 1110/1068, the olivine data suggests that the enriched component was added to system prior to olivine crystallization.  相似文献   

7.
Abstract– Northwest Africa (NWA) 1068 is one of the few olivine‐phyric shergottites (e.g., NWA 1068, Larkman Nunatak [LAR] 06319, and Roberts Massif [RBT] 04262) that is not depleted in light rare earth elements (LREE). Its REE pattern is similar to that of the basaltic shergottite Shergotty, suggesting a possible connection between the olivine‐phyric and the basaltic shergottites. To test this possible link, we have investigated the high‐pressure near‐liquidus phase equilibria for the NWA 1068 meteorite bulk composition. Our results show that the NWA 1068 bulk composition does not represent an unmodified mantle‐derived melt; the olivine and pyroxene in our near‐liquidus experiments are more magnesian than in the rock itself, which suggests that NWA 1068 contains cumulate minerals (extra olivine). We have then used these experimental results combined with the pyroxene compositions in NWA 1068 to constrain the possible high‐pressure crystallization history of the parental magma. These results suggest that NWA 1068 had a complex polybaric history. Finally, we have calculated a model parental magma composition for the NWA 1068 meteorite. The calculated parental magma is an evolved basaltic composition which is too ferroan to be a primitive melt directly derived from the mantle. We suggest that it ponded and crystallized at approximately the base of the crust. This provided an opportunity for the magma to become contaminated by an “enriched” crustal component prior to crystallization. The results and modeling from these experiments are applicable not only to the NWA 1068 meteorite, but also to LAR 06319 and possibly any other enriched olivine‐phyric shergottite.  相似文献   

8.
Asuka (A) 12325 is the first poikilitic shergottite having a depleted pattern in light rare earth elements (REE). Compared with known poikilitic shergottites, A 12325 has smaller but more abundant pyroxene oikocrysts with remarkable Fe-rich pigeonite rims, indicating that A 12325 cooled relatively faster at a shallower part of the crust. The redox condition (logfO2 = IW + 0.6-IW + 1.7) and Fe-rich chemical compositions of each mineral in A 12325 are close to enriched shergottites. The intermediate shergottites could not form by a simple mixing between parent magmas of A 12325 and enriched shergottites. Although A 12325 contains various high-pressure minerals such as majorite and ringwoodite, plagioclase is only partly maskelynitized. Therefore, the maximum shock pressure may be within 17–22 GPa. Thermal conduction and ringwoodite growth calculation around a shock vein revealed that the shock dwell time of A 12325 is at least 40 ms. The weaker shock pressure and longer shock dwell time in A 12325 may be attained by an impact event similar to those of nakhlites and Northwest Africa (NWA) 8159. Such a weak shock ejection event may be as common on Mars as a severe shock event recorded in shergottites. Alteration of sulfide observed in A 12325 may imply the presence of magmatic fluid in its reservoir on Mars. A 12325 expands a chemical variety of Martian rocks and has a unique shock history among poikilitic shergottites while A 12325 also implies that poikilitic shergottites are common rocks on Mars regardless of their sources.  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— Radiometric age dating of the shergottite meteorites and cratering studies of lava flows in Tharsis and Elysium both demonstrate that volcanic activity has occurred on Mars in the geologically recent past. This implies that adiabatic decompression melting and upwelling convective flow in the mantle remains important on Mars at present. I present a series of numerical simulations of mantle convection and magma generation on Mars. These models test the effects of the total radioactive heating budget and of the partitioning of radioactivity between crust and mantle on the production of magma. In these models, melting is restricted to the heads of hot mantle plumes that rise from the core‐mantle boundary, consistent with the spatially localized distribution of recent volcanism on Mars. For magma production to occur on present‐day Mars, the minimum average radioactive heating rate in the martian mantle is 1.6 times 10?12 W/kg, which corresponds to 39% of the Wanke and Dreibus (1994) radioactivity abundance. If the mantle heating rate is lower than this, the mean mantle temperature is low, and the mantle plumes experience large amounts of cooling as they rise from the base of the mantle to the surface and are, thus, unable to melt. Models with mantle radioactive heating rates of 1.8 to 2.1 times 10 ?12 W/kg can satisfy both the present‐day volcanic resurfacing rate on Mars and the typical melt fraction observed in the shergottites. This corresponds to 43–50% of the Wanke and Dreibus radioactivity remaining in the mantle, which is geochemically reasonable for a 50 km thick crust formed by about 10% partial melting. Plausible changes to either the assumed solidus temperature or to the assumed core‐mantle boundary temperature would require a larger amount of mantle radioactivity to permit present‐day magmatism. These heating rates are slightly higher than inferred for the nakhlite source region and significantly higher than inferred from depleted shergottites such as QUE 94201. The geophysical estimate of mantle radioactivity inferred here is a global average value, while values inferred from the martian meteorites are for particular points in the martian mantle. Evidently, the martian mantle has several isotopically distinct compositions, possibly including a radioactively enriched source that has not yet been sampled by the martian meteorites. The minimum mantle heating rate corresponds to a minimum thermal Rayleigh number of 2 times 106, implying that mantle convection remains moderately vigorous on present‐day Mars. The basic convective pattern on Mars appears to have been stable for most of martian history, which has prevented the mantle flow from destroying the isotopic heterogeneity.  相似文献   

11.
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   

12.
We determined the chlorine isotope composition of 16 Martian meteorites using gas source mass spectrometry on bulk samples and in situ secondary ion microprobe analysis on apatite grains. Measured δ37Cl values range from ?3.8 to +8.6‰. The olivine‐phyric shergottites are the isotopically lightest samples, with δ37Cl mostly ranging from ?4 to ?2‰. Samples with evidence for a crustal component have positive δ37Cl values, with an extreme value of 8.6‰. Most of the basaltic shergottites have intermediate δ37Cl values of ?1 to 0‰, except for Shergotty, which is similar to the olivine‐phyric shergottites. We interpret these data as due to mixing of a two‐component system. The first component is the mantle value of ?4 to ?3‰. This most likely represents the original bulk Martian Cl isotope value. The other endmember is a 37Cl‐enriched crustal component. We speculate that preferential loss of 35Cl to space has resulted in a high δ37Cl value for the Martian surface, similar to what is seen in other volatile systems. The basaltic shergottites are a mixture of the other two endmembers. The low δ37Cl value of primitive Mars is different from Earth and most chondrites, both of which are close to 0‰. We are not aware of any parent‐body process that could lower the δ37Cl value of the Martian mantle to ?4 to ?3‰. Instead, we propose that this low δ37Cl value represents the primordial bulk composition of Mars inherited during accretion. The higher δ37Cl values seen in many chondrites are explained by later incorporation of 37Cl‐enriched HCl‐hydrate.  相似文献   

13.
We conducted a petrologic study of apatite within 12 Martian meteorites, including 11 shergottites and one basaltic regolith breccia. These data were combined with previously published data to gain a better understanding of the abundance and distribution of volatiles in the Martian interior. Apatites in individual Martian meteorites span a wide range of compositions, indicating they did not form by equilibrium crystallization. In fact, the intrasample variation in apatite is best described by either fractional crystallization or crustal contamination with a Cl‐rich crustal component. We determined that most Martian meteorites investigated here have been affected by crustal contamination and hence cannot be used to estimate volatile abundances of the Martian mantle. Using the subset of samples that did not exhibit crustal contamination, we determined that the enriched shergottite source has 36–73 ppm H2O and the depleted source has 14–23 ppm H2O. This result is consistent with other observed geochemical differences between enriched and depleted shergottites and supports the idea that there are at least two geochemically distinct reservoirs in the Martian mantle. We also estimated the H2O, Cl, and F content of the Martian crust using known crust‐mantle distributions for incompatible lithophile elements. We determined that the bulk Martian crust has ~1410 ppm H2O, 450 ppm Cl, and 106 ppm F, and Cl and H2O are preferentially distributed toward the Martian surface. The estimate of crustal H2O results in a global equivalent surface layer (GEL) of ~229 m, which can account for at least some of the surface features on Mars attributed to flowing water and may be sufficient to support the past presence of a shallow sea on Mars' surface.  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— 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   

16.
Grove Mountains (GRV) 020090 is an enriched lherzolitic shergottite, distinct from other lherzolitic shergottites, except RBT 04262/1. Its characteristics include high abundance of plagioclase (24.2 vol% in the nonpoikilitic area), presence of K‐feldspar, common occurrence of baddeleyite, high FeO contents of olivine (bimodal peaks at Fa 33 mol% and Fa 41 mol%) and low‐Ca pyroxenes (bimodal peaks at Fs 23.8–31.7 mol% and Fs 25.7–33.9 mol%), and significant LREE enrichment of phosphates (500–610 × CI). The bulk composition of GRV 020090 suggests derivation from partial melting of an enriched reservoir. However, the REE patterns of the cores of pigeonite oikocrysts and the olivine chadacrysts are indistinguishable from those of GRV 99027 and other moderately depleted lherzolitic shergottites, and reveal a LREE‐depleted pattern of the primordial parent magma. We propose that the primordial parent magma of GRV 020090 was derived from a moderately depleted Martian upper mantle reservoir, and later the residual melt was contaminated by oxidized and enriched Martian crustal materials as it ascended up to the subsurface. GRV 020090 and RBT 04262/1 may have sampled an igneous unit different from other lherzolitic shergottites.  相似文献   

17.
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   

18.
Olivine‐phyric shergottites represent primitive basaltic to picritic rocks, spanning a large range of Mg# and olivine abundances. As primitive olivine‐bearing magmas are commonly representative of their mantle source on Earth, understanding the petrology and evolution of olivine‐phyric shergottites is critical in our understanding of Martian mantle compositions. We present data for the olivine‐phyric shergottite Northwest Africa (NWA) 10170 to constrain the petrology with specific implications for magma plumbing‐system dynamics. The calculated oxygen fugacity and bulk‐rock REE concentrations (based on modal abundance) are consistent with a geochemically intermediate classification for NWA 10170, and overall similarity with NWA 6234. In addition, we present trace element data using laser ablation ICP‐MS for coarse‐grained olivine cores, and compare these data with terrestrial and Martian data sets. The olivines in NWA 10170 contain cores with compositions of Fo77 that evolve to rims with composition of Fo58, and are characterized by cores with low Ni contents (400–600 ppm). Nickel is compatible in olivine and such low Ni content for olivine cores in NWA 10170 suggests either early‐stage fractionation and loss of olivine from the magma in a staging chamber at depth, or that Martian magmas have lower Ni than terrestrial magmas. We suggest that both are true in this case. Therefore, the magma does not represent a primary mantle melt, but rather has undergone 10–15% fractionation in a staging chamber prior to extrusion/intrusion at the surface of Mars. This further implies that careful evaluation of not only the Mg# but also the trace element concentrations of olivine needs to be conducted to evaluate pristine mantle melts versus those that have fractionated olivine (±pyroxene and oxide minerals) in staging chambers.  相似文献   

19.
Abstract– The oxygen fugacities recorded in the nakhlites Nakhla, Yamato‐000593 (Y‐000593), Lafayette, and NWA998 were studied by applying the Fe,Ti‐oxide oxybarometer. Oxygen fugacities obtained cluster closely around the FMQ (Fayalite–Magnetite–Quartz) buffer (NWA998 = FMQ ? 0.8; Y‐000593 = FMQ ? 0.7; Nakhla = FMQ; Lafayette = FMQ + 0.1). The corresponding equilibration temperatures are 810 °C for Nakhla and Y‐000593, 780 °C for Lafayette and 710 °C for NWA998. All nakhlites record oxygen fugacities significantly higher and with a tighter range than those determined for Martian basalts, i.e., shergottites whose oxygen fugacities vary from FMQ ? 1 to FMQ ? 4. It has been known for some time that nakhlites are different from other Martian meteorites in chemistry, mineralogy, and crystallization age. The present study adds oxygen fugacity to this list of differences. The comparatively large variation in fO2 recorded by shergottites was interpreted by Herd et al. (2002) as reflecting variable degrees of contamination with crustal fluids that would also carry a light rare earth element (REE)‐enriched component. The high oxygen fugacities and the large light REE enrichment of nakhlites fit qualitatively in this model. In detail, however, it is found that the inferred contaminating phase in nakhlites must have been different from those in shergottites. This is supported by unique 182W/184W and 142Nd/144Nd ratios in nakhlites, which are distinct from other Martian meteorites. It is likely that the differences in fO2 between nakhlites and other Martian meteorites were established very early in the history of Mars. Parental trace element rich and trace element poor regions (reservoirs) of Mars mantle ( Brandon et al. 2000 ) must have been kept isolated throughout Martian history. Our results further show significant differences in closure temperature among the different nakhlites. The observed range in equilibration temperatures together with similar fO2 values is attributable to crystallization of nakhlites in the same cumulate pile or lava layer at different burial depths from 0.5 to 30 m below the Martian surface in agreement with Mikouchi et al. (2003) and is further confirmed by similar crystallization ages of about 1.3 Ga ago (e.g., Misawa et al. 2003 ).  相似文献   

20.
Abstract— We report petrography, mineral chemistry, and microdistribution of rare earth elements (REE) in a new lherzolitic shergottite, Grove Mountains (GRV) 99027. The textural relationship and REE patterns of minerals suggest precipitation of cumulus olivine and chromite, followed by equilibrium crystallization of a closed system with a bulk composition of the inferred intercumulus melt. Subsolidus equilibrium temperatures of pyroxenes and olivine range from 1100 to 1210 °C, based on a two‐pyroxene thermometry and Ca partitioning between augite and olivine. Oxygen fugacity of the parent magma is 1.5–2.5 (av. 2.0 ± 0.4) log units below the quartz‐fayalite‐magnetite (QFM) buffer at 960–1360 °C, according to the olivine‐orthopyroxene‐chromite barometer. The ilmenite‐chromite barometer and thermometer show much wider ranges of oxygen fugacity (1.0–7.0 log unit below QFM) and temperature (1130–480 °C), suggesting subsolidus equilibration of the oxides at low temperatures, probably due to deep burial of GRV 99027 on Mars. The low oxygen fugacity and LREE depletion of the parent magma of GRV 99027 suggest low contamination by martian crust. Characteristics of GRV 99027 demonstrate similarity of lherzolitic shergottites, suggesting a high possibility of launch pairing or a homogeneous upper mantle of Mars if they were ejected by individual impact events. However, GRV 99027 probably experienced severe post‐shock thermal metamorphism in comparison with other lherzolitic shergottites, based on the re‐crystallization of maskelynite, the homogeneity of minerals, and the low subsolidus equilibrium temperatures between chromite and ilmenite.  相似文献   

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