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1.
Abstract Terrestrial alteration of meteorites results in the redistribution, gain, or loss of uranium and other elements. We have measured the maximum U adsorption capacity of a meteorite and two geochemical reference materials under conditions resembling terrestrial ones (pH 5.8). The basaltic eucrite Sioux County adsorbs 7 ppm of U. The result for the terrestrial granite AC‐E is similar (5 ppm), while the basalt BE‐N adsorbs 34 ppm of U. We have also investigated U adsorption in the presence of phosphate (0.01 M or less) in imitation of conditions that probably occurred in the earlier history of Mars. Such a process would have alterated Martian surface material and would be noticeable in Martian meteorites from the affected surface. The experiments demonstrated the counteracting effects of phosphate, which increases U adsorption, but decreases the quantity of dissolved U that is available for adsorption. U adsorption by AC‐E increases to 7 ppm. The lowered value for BE‐N of 8 ppm results from the low quantity of dissolved U in the volume of solution used. The results from the adsorption experiments and from leaching the Martian meteorite Zagami and a terrestrial basalt imply that the aqueous redistribution of U on Mars was moderate. Acidic liquids mobilized uranium and other metals, but present phosphate impeded the dissolution of U compounds. Some mobilized U may have reached the global sinks, while most of it probably was transported in the form of suspended particles over a limited distance and then settled.  相似文献   

2.
Hydrous alteration of olivine macrocrysts in a Martian olivine phyric basalt, NWA 10416, and a terrestrial basalt from southern Colorado are examined using SEM, EPMA, TEM, and µXRD techniques. The olivines in the meteorite contain linear nanotubes of hydrous material, amorphous areas, and fluid dissolution textures quite distinct from alteration identified in other Martian meteorites. Instead, they bear resemblance to terrestrial deuteric alteration features. The presence of the hydrous alteration phase Mg‐laihunite within the olivines has been confirmed by µXRD analysis. The cores of the olivines in both Martian and terrestrial samples are overgrown by unaltered rims whose compositions match those of a separate population of groundmass olivines, suggesting that the core olivines are xenocrysts whose alteration preceded crystallization of the groundmass. The terrestrial sample is linked to deep crustal metasomatism and the “ignimbrite flare‐up” of the Oligocene epoch. The comparison of the two samples suggests the existence of an analogous relatively water‐rich magmatic reservoir on Mars.  相似文献   

3.
Abstract— Major element and sulfur concentrations have been determined in experimentally heated olivine‐hosted melt inclusions from a suite of Apollo 12 picritic basalts (samples 12009, 12075, 12020, 12018, 12040, 12035). These lunar basalts are likely to be genetically related by olivine accumulation (Walker et al. 1976a, b). Our results show that major element compositions of melt inclusions from samples 12009, 12075, and 12020 follow model crystallization trends from a parental liquid similar in composition to whole rock sample 12009, thereby partially confirming the olivine accumulation hypothesis. In contrast, the compositions of melt inclusions from samples 12018, 12040, and 12035 fall away from model crystallization trends, suggesting that these samples crystallized from melts compositionally distinct from the 12009 parent liquid and therefore may not be strictly cogenetic with other members of the Apollo 12 picritic basalt suite. Sulfur concentrations in melt inclusions hosted in early crystallized olivine (Fo75) are consistent with a primary magmatic composition of 1050 ppm S, or about a factor of 2 greater than whole rock compositions with 400–600 ppm S. The Apollo 12 picritic basalt parental magma apparently experienced outgassing and loss of S during transport and eruption on the lunar surface. Even with the higher estimates of primary magmatic sulfur concentrations provided by the melt inclusions, the Apollo 12 picritic basalt magmas would have been undersaturated in sulfide in their mantle source regions and capable of transporting chalcophile elements from the lunar mantle to the surface. Therefore, the measured low concentration of chalcophile elements (e.g., Cu, Au, PGEs) in these lavas must be a primary feature of the lunar mantle and is not related to residual sulfide remaining in the mantle during melting. We estimate the sulfur concentration of the Apollo 12 mare basalt source regions to be ～75 ppm, which is significantly lower than that of the terrestrial mantle.  相似文献   

4.
Meteorites, generally 1 cm or larger in size that are believed to sample asteroids, and interplanetary dust particles (IDPs), generally 5–50 μm in size that are believed to sample both asteroids and comets, span the size range of the meteors. Thus, the physical properties of the meteorites and the IDPs are likely to constrain the properties of the meteors and their parent bodies. Measurements of the density, porosity, longitudinal and transverse speeds of sound, elastic modulus, and bulk modulus, as well as imaging of the internal structure by Computed Microtomography indicate that unweathered samples of chondritic meteorites are more porous and have lower sound velocities than compact terrestrial rocks. In general, the IDPs are even more porous than the chondritic meteorites. The impact energy per unit target mass required to produce a barely catastrophic disruption (Q * D) for anhydrous ordinary chondrite meteorites is twice that for terrestrial basalt or glass, indicating that collisional disruption of anhydrous meteorites requires more energy than for a compact basalt. These results indicate that most stone meteors are likely to be weak, porous objects, and that the parent bodies of the anhydrous stone meteorites are likely to be more difficult to disrupt than compact terrestrial basalt.  相似文献   

5.
Remotely sensed observations from recent missions (e.g., GRAIL, Kaguya, Chandrayaan‐1) have been interpreted as indicating that the deep crust and upper mantle are close to or at the lunar surface in many large impact basins (e.g., Crisium, Apollo, Moscoviense). If this is correct, the capability of either impact or volcanic processes to transport mantle lithologies to the lunar surface should be enhanced in these regions. Somewhat problematic to these observations and interpretations is that examples of mantle lithologies in the lunar sample collection (Apollo Program, Luna Program, lunar meteorites) are at best ambiguous. Dunite xenoliths in high‐Ti mare basalt 74275 are one of these ambiguous examples. In this high‐Ti mare basalt, olivine occurs in three generations: olivine associated with dunite xenoliths, olivine megacrysts, and olivine microphenocrysts. The dunite xenoliths are anhedral in shape and are generally greater than 800 μm in diameter. The interior of the xenoliths are fairly homogeneous with regard to many divalent cations. For example, the Mg# (Mg/Mg + Fe × 100) ranges from 82 to 83 in their interiors and decreases from 82 to 68 over the 10–30 μm wide outer rim. Titanium and phosphorus X‐ray maps of the xenolith illustrate that these slow diffusing elements preserve primary cumulate zoning textures. These textures indicate that the xenoliths consist of many individual olivine grains approximately 150–200 μm in diameter with low Ti, Al, and P cores. These highly incompatible elements are enriched in the outer Fe‐rich rims of the xenoliths and slightly enriched in the rims of the individual olivine grains. Highly compatible elements in olivine such as Ni exhibit a decrease in the rim surrounding the xenolith, an increase in the incompatible element depleted cores of the individual olivine grains, and a slight decrease in the “interior rims” of the individual olivine grains. Inferred melt composition, liquid lines of descent, and zoning profiles enable the reconstruction of the petrogenesis of the dunite xenoliths. Preservation of primary magmatic zoning (Ti, P, Al) and lack of textures similar to high‐pressure mineral assemblages exhibited by the Mg‐suite (Shearer et al. 2015) indicate that these xenoliths do not represent deep crustal or shallow mantle lithologies. Further, they are chemically and mineralogically distinct from Mg‐suite dunites identified from the Apollo 17 site. More likely, they represent olivine cumulates that crystallized from a low‐Ti mare basalt at intermediate to shallow crustal levels. The parent basalt to the dunite xenolith lithology was more primitive than low‐Ti basalts thus far returned from the Moon. Furthermore, this parental magma and its more evolved daughter magmas are not represented in the basalt sample suite returned from the Taurus‐Littrow Valley by the Apollo 17 mission. The dunite xenolith records several episodes of crystallization and re‐equilibration. During the last episode of re‐equilibration, the dunite cumulate was sampled by the 74275 high‐Ti basalt and transported over a period of 30–70 days to the lunar surface.  相似文献   

6.
Phosphorus zoning is observed in olivines in high‐FeO (type IIA) chondrules in H chondrites over the entire range of petrologic grades: H3.1–H6. Features in P concentrations such as oscillatory and sector zoning, and high P cores are present in olivines that are otherwise unzoned in the divalent cations. Aluminum concentrations are low and not significantly associated with P zoning in chondrule olivines. In highly unequilibrated H chondrites, phosphorus zoning is generally positively correlated with Cr. Atomic Cr:P in olivine is roughly 1:1 (3:1 for one zone in one olivine in RC 075), consistent with Cr3+ charge‐balancing P5+ substituting for Si4+. Normal igneous zonation involving the dominant chrome species Cr2+ was observed only in the LL3.0 chondrite Semarkona. In more equilibrated chondrites (H3.5–H3.8), Cr spatially correlated with P is occasionally observed but it is diffuse relative to the P zones. In H4–H6 chondrites, P‐correlated Cr is absent. One signature of higher metamorphic grades (≥H3.8) is the presence of near matrix olivines that are devoid of P oscillatory zoning. The restriction to relatively high metamorphic grade and to grains near the chondrule–matrix interface suggests that this is a response to metasomatic processes. We also observed P‐enriched halos near the chondrule–matrix interface in H3.3–H3.8 chondrites, likely reflecting the loss of P and Ca from mesostasis and precipitation of Ca phosphate near the chondrule surface. These halos are absent in equilibrated chondrites due to coarsening of the phosphate and in unequilibrated chondrites due to low degrees of metasomatism. Olivines in type IA chondrules show none of the P‐zoning ubiquitous in type IIA chondrules or terrestrial igneous olivines, likely reflecting sequestration of P in reduced form within metallic alloys and sulfides during melting of type IA chondrules.  相似文献   

7.
Abstract— We report here the petrography, mineralogy, and geochemistry of lunar meteorite Sayh al Uhaymir 300 (SaU 300). SaU 300 is dominated by a fine‐grained crystalline matrix surrounding mineral fragments (plagioclase, pyroxene, olivine, and ilmenite) and lithic clasts (mainly feldspathic to noritic). Mare basalt and KREEPy rocks are absent. Glass melt veins and impact melts are present, indicating that the rock has been subjected to a second impact event. FeNi metal and troilite grains were observed in the matrix. Major element concentrations of SaU 300 (Al2O3 21.6 wt% and FeO 8.16 wt%) are very similar to those of two basalt‐bearing feldspathic regolith breccias: Calcalong Creek and Yamato (Y‐) 983885. However, the rare earth element (REE) abundances and pattern of SaU 300 resemble the patterns of feldspathic highlands meteorites (e.g., Queen Alexandra Range (QUE) 93069 and Dar al Gani (DaG) 400), and the average lunar highlands crust. It has a relatively LREE‐enriched (7 to 10 x CI) pattern with a positive Eu anomaly (?11 x CI). Values of Fe/Mn ratios of olivine, pyroxene, and the bulk sample are essentially consistent with a lunar origin. SaU 300 also contains high siderophile abundances with a chondritic Ni/Ir ratio. SaU 300 has experienced moderate terrestrial weathering as its bulk Sr concentration is elevated compared to other lunar meteorites and Apollo and Luna samples. Mineral chemistry and trace element abundances of SaU 300 fall within the ranges of lunar feldspathic meteorites and FAN rocks. SaU 300 is a feldspathic impact‐melt breccia predominantly composed of feldspathic highlands rocks with a small amount of mafic component. With a bulk Mg# of 0.67, it is the most mafic of the feldspathic meteorites and represents a lunar surface composition distinct from any other known lunar meteorites. On the basis of its low Th concentration (0.46 ppm) and its lack of KREEPy and mare basaltic components, the source region of SaU 300 could have been within a highland terrain, a great distance from the Imbrium impact basin, probably on the far side of the Moon.  相似文献   

8.
The concentrations of major and trace elements have been determined in igneous rocks from Apollo 15. All materials analyzed have typical depletions of Eu except for minerals separated from sample 15085. Four samples have concentrations of trace elements that are similar to those of KREEP. The samples of mare basalt from Apollo 15 have higher concentrations of FeO, MgO, Mn, and Cr and lower concentrations of CaO, Na2O, K2O, and rare-earth elements (REE) as compared to the samples of mare basalt from Apollos 11, 12, and 14. The samples can be divided into two groups on the basis of their normative compositions. One group is quartz normative and has low concentrations of FeO while the other is olivine normative and has high concentrations of FeO. The trace element data indicate that the samples of olivine normative basalt could be from different portions of a single lava flow. At least two and possible three parent magmas can be identified from the samples of the quartz normative group on the basis of their concentration ratios of Sm to Eu. Within each group, the compositions of the samples appear to be related by crystallization of olivine or pyroxene. Significant variations of the ratio of concentration of Sm to Eu cannot be produced without plagioclase-liquid equilibrium. The source material of mare basalt may be depleted in Eu. Alternatively, the magmas may have assimilated a small volume of material similar to KREEP.Paper dedicated to Prof. Harold C. Urey on the occasion of his 80th birthday on 29 April 1973.  相似文献   

9.
Abstract— We present new compositional data for 30 lunar stones representing about 19 meteorites. Most have iron concentrations intermediate to those of the numerous feldspathic lunar meteorites (3–7% FeO) and the basaltic lunar meteorites (17–23% FeO). All but one are polymict breccias. Some, as implied by their intermediate composition, are mainly mixtures of brecciated anorthosite and mare basalt, with low concentrations of incompatible elements such as Sm (1–3 μg/g). These breccias likely originate from points on the Moon where mare basalt has mixed with material of the FHT (Feldspathic Highlands Terrane). Others, however, are not anorthosite‐basalt mixtures. Three (17–75 μ/g Sm) consist mainly of nonmare mafic material from the nearside PKT (Procellarum KREEP Terrane) and a few are ternary mixtures of material from the FHT, PKT, and maria. Some contain mafic, nonmare lithologies like anorthositic norites, norites, gabbronorites, and troctolite. These breccias are largely unlike breccias of the Apollo collection in that they are poor in Sm as well as highly feldspathic anorthosite such as that common at the Apollo 16 site. Several have high Th/Sm compared to Apollo breccias. Dhofar 961, which is olivine gabbronoritic and moderately rich in Sm, has lower Eu/Sm than Apollo samples of similar Sm concentration. This difference indicates that the carrier of rare earth elements is not KREEP, as known from the Apollo missions. On the basis of our present knowledge from remote sensing, among lunar meteorites Dhofar 961 is the one most likely to have originated from South Pole‐Aitken basin on the lunar far side.  相似文献   

10.
Abstract Detailed analysis of cumulate and melt inclusion assemblages in the chassignites provide important constraints on the nature of the melt trapped as inclusions in cumulus olivine (and, by extension, parental magma compositions), the pressures of crystallization, and magmatic volatile contents. These mineral assemblages show strong similarities to the experimental fractionation assemblages that produce the sodic silica‐saturated alkalic lavas on Earth (e.g., Ascension Island, Azores, the Nandewar volcano of Australia). The experimental assemblages were produced from silica‐saturated hawaiite at pressures above 4.3 kbar with dissolved water contents above 0.5 wt%. Such pressures are consistent with Ti:Al ratios of the melt‐inclusion pyroxenes in the Chassigny meteorite. Pyroxene compositions suggest early high crystallization temperatures and thus relatively low initial water and F contents. Feldspars indicate that melt evolution proceeded to rhyolite compositions both within the interstices of the cumulate olivine and within the melt inclusions, even though rhyolitic glass is only found within olivine‐hosted polyphase melt inclusions. The observed rhyolite glass is compositionally similar to the alkali‐rich rhyolite of Ascension Island which is produced experimentally by crystallization of hawaiite. It is proposed that the melt trapped in cumulus olivine of the Chassigny dunite was similar to a terrestrial silica‐saturated hawaiite, while that trapped in olivine of the Northwest Africa (NWA) 2727 dunite was less evolved, perhaps mildly alkalic basalt. Melts similar to terrestrial intra‐plate tholeiite could be parental to the cumulus minerals and evolve upon crystallization at pressures above 4.3 kbar and water contents above ?0.4 wt% to mildly alkalic basalt, silica‐saturated hawaiite, and alkali‐rich rhyolite. The melt inclusion assemblages are inconsistent with either crystallization of a low‐Al, high‐Fe basalt, or low‐pressure crystallization of a terrestrial‐like tholeiite.  相似文献   

11.
The HRSC (image 0037) and MOC imagery and MOLA altimetry were used to determine the following parameters of the lava flows typical of the southern slope of the Martian volcano Olympus: the length (13–35 km), the width (0.2–4.8 km), and the angles of ground slopes along which these flows advanced (3.4°–6.9°). To measure the thickness of the flows, we applied a method which had never been used before for Mars. In this method, the apparent thickness obtained from the MOC images and the slope steepness obtained from the MOLA data are used to determine the true thickness. The average estimates of the thickness of lava flows vary from 4 to 11 m and from 4 to 26 m for the volcano flanks and caldera scarps, respectively. These values are close to those of terrestrial basalt flows and to the lower limit found for the Martian flows by other researchers. Based on the performed measurements, we estimated the lava yield strength (0.9 × 103?3.6 × 104 Pa), the supply rate (24–137 m3/s), and the viscosity (1.4 × 103?2.8 × 107 kg/m s). These values are close to the estimates found for the Martian lavas by other researchers and to the characteristic values of these parameters for terrestrial lava flows with basalt and basalt-andesite composition.  相似文献   

12.
Abstract– Analyses by the Mars Exploration Rover (MER), Spirit, of Martian basalts from Gusev crater show that they are chemically very different from terrestrial basalts, being characterized in particular by high Mg‐ and Fe‐contents. To provide suitable analog basalts for the International Space Analogue Rockstore (ISAR), a collection of analog rocks and minerals for preparing in situ space missions, especially, the upcoming Mars mission MSL‐2011 and the future international Mars‐2018 mission, it is necessary to synthesize Martian basalts. The aim of this study was therefore to synthesize Martian basalt analogs to the Gusev crater basalts, based on the geochemical data from the MER rover Spirit. We present the results of two experiments, one producing a quench‐cooled basalt (<1 h) and one producing a more slowly cooled basalt (1 day). Pyroxene and olivine textures produced in the more slowly cooled basalt were surprisingly similar to spinifex textures in komatiites, a volcanic rock type very common on the early Earth. These kinds of ultramafic rocks and their associated alteration products may have important astrobiological implications when associated with aqueous environments. Such rocks could provide habitats for chemolithotrophic microorganisms, while the glass and phyllosilicate derivatives can fix organic compounds.  相似文献   

13.
Paul D. Komar 《Icarus》1980,42(3):317-329
Depending on their grain sizes (settling velocities), sediments are transported in rivers as bed load, in suspension, or as wash load. The coarsest material rolls or bounces along the bottom as bed load whereas finer material is placed into suspension by the water turbulence. The finest sediments are transported as wash load, evenly distributed through the water depth and effectively moving at the same rate as the water. The criteria for quantitatively determining which grain-size ranges are being transported in terrestrial rivers as bed load, suspended load and wash load are applied to an analysis of sediment transport in the large Martian outflow channels, assuming their origin to have been from water flow. Of importance is the balance of the effects of the reduced Martian gravity on the water flow velocity versus the reduction in grain settling velocities. Analyses were performed using grain densities ranging from 2.90 g/cm3 (basalt) to 1.20 g/cm3 (volcanic ash). The results show that the Martian flows could have transported cobbles in suspension and that nearly all sand-size material and finer would have been transported as wash load. Wash-load transport requires little or no net expenditure of the water-flow power, so the sands and finer could have been carried in nearly unlimited quantities. A comparison with terrestrial rivers indicates that concentrations as high as 60–70% by weight of wash-load sediment could have prevailed in the Martian flows, resulting in the very rapid erosion of the channels.  相似文献   

14.
Shatter cones are one of the most widely recognized pieces of evidence for meteorite impact events on Earth, but the process responsible for their formation is still debated. Evidence of melting on shatter cone surfaces has been rarely reported in the literature from terrestrial impact craters but has been recently observed in impact experiments. Although several models for shatter cones formation have been proposed, so far, no one can explain all the observed features. Shatter cones' from the Vista Alegre impact structure, Brazil, formed in fine‐grained basalt of the Jurassic‐Cretaceous Serra Geral Formation (Paraná large igneous province). A continuous quenched melt film, consisting of a crystalline phase, mica, and amorphous material, decorates the striated surface. Ultracataclasites, containing subrounded pyroxene clasts in an ultrafine‐grained matrix, occur subparallel to the striated surface. Several techniques were applied to characterize the crystalline phase in the melt, including Raman spectroscopy and transmission electron microscopy. Results are not consistent with any known mineral, but they do suggest a possible rare or new type of clinopyroxene. This peculiar evidence of melting and cataclasis in relation with shatter cone surfaces is interpreted as the result of tensile fracturing at the tip of a fast propagating shock‐induced rupture, which led to the formation of shatter cones at the tail of the shock front, likely during the early stage of the impact events.  相似文献   

15.
The behavior of rare earth elements (REEs) during hot desert weathering of meteorites is investigated. Ordinary chondrites (OCs) from Atacama (Chile) and Lut (Iran) deserts show different variations in REE composition during this process. Inductively coupled plasma–mass spectrometry (ICP‐MS) data reveal that hot desert OCs tend to show elevated light REE concentrations, relative to OC falls. Chondrites from Atacama are by far the most enriched in REEs and this enrichment is not necessarily related to their degree of weathering. Positive Ce anomaly of fresh chondrites from Atacama and the successive formation of a negative Ce anomaly with the addition of trivalent REEs are similar to the process reported from Antarctic eucrites. In addition to REEs, Sr and Ba also show different concentrations when comparing OCs from different hot deserts. The stability of Atacama surfaces and the associated old terrestrial ages of meteorites from this region give the samples the necessary time to interact with the terrestrial environment and to be chemically modified. Higher REE contents and LREE‐enriched composition are evidence of contamination by terrestrial soil. Despite their low degrees of weathering, special care must be taken into account while working on the REE composition of Atacama meteorites for cosmochemistry applications. In contrast, chondrites from the Lut desert show lower degrees of REE modification, despite significant weathering signed by Sr content. This is explained by the relatively rapid weathering rate of the meteorites occurring in the Lut desert, which hampers the penetration of terrestrial material by forming voluminous Fe oxide/oxyhydroxides shortly after the meteorite fall.  相似文献   

16.
Abstract— Northwest Africa 482 (NWA 482) is a crystalline impact‐melt breccia from the Moon with highlands affinities. The recrystallized matrix and the clast population are both highly anorthositic. Clasts are all related to the ferroan anorthosite suite, and include isolated plagioclase crystals and lithic anorthosites, troctolites, and spinel troctolites. Potassium‐, rare‐earth‐element‐, and phosphorus‐bearing (KREEP) and mare lithologies are both absent, constraining the source area of this meteorite to a highland terrain with little to no KREEP component, most likely on the far side of the Moon. Glass is present in shock veins cutting through the sample and in several large melt pockets, indicating a second impact event. There are two separate events recorded in the 40Ar‐39Ar system: one at ～3750 Ma, which completely reset the K‐Ar system, and one at ?2400 Ma, which caused only partial degassing. These events could represent, respectively, crystallization of the impact‐melt breccia and later formation of the glass, or the formation of the glass and a later thermal event. The terrestrial age of the meteorite is 8.6 ± 1.3 ka. This age corresponds well with the modest amount of weathering in the rock, in the form of secondary phyllosilicates and carbonates. Based on terrestrial age and location, lithology, and chemistry, NWA 482 is unique among known lunar meteorites.  相似文献   

17.
Abstract– Sixty named lunar meteorite stones representing about 24 falls have been found in Oman. In an area of 10.7 × 103 km2 in southern Oman, lunar meteorite areal densities average 1 g km?2. All lunar meteorites from Oman are breccias, although two are dominated by large igneous clasts (a mare basalt and a crystalline impact‐melt breccia). Among the meteorites, the range of compositions is large: 9–32% Al2O3, 2.5–21.1% FeO, 0.3–38 μg g?1 Sm, and <1 to 22.5 ng g?1 Ir. The proportion of nonmare lunar meteorites is higher among those from Oman than those from Antarctica or Africa. Omani lunar meteorites extend the compositional range of lunar rocks as known from the Apollo collection and from lunar meteorites from other continents. Some of the feldspathic meteorites are highly magnesian (high MgO/[MgO + FeO]) compared with most similarly feldspathic Apollo rocks. Two have greater concentrations of incompatible trace elements than all but a few Apollo samples. A few have moderately high abundances of siderophile elements from impacts of iron meteorites on the Moon. All lunar meteorites from Oman are contaminated, to various degrees, with terrestrial Na, K, P, Zn, As, Se, Br, Sr, Sb, Ba, U, carbonates, or sulfates. The contamination is not so great, however, that it seriously compromises the scientific usefulness of the meteorites as samples from randomly distributed locations on the Moon.  相似文献   

18.
Abstract— Concentrations of adsorbed water in single mineral grains of Antarctic lunar meteorites were determined with micro infrared (IR) spectroscopy. A relationship was found between the mineral's ability to adsorb water and the extent of Ce anomaly in rare earth element (REE) patterns precisely determined by the isotope dilution method using a thermal ionization mass spectrometer. Asuka (A) 881757, a lunar meteorite from the mare basalt without Ce anomaly, showed no trace of IR absorption due to adsorbed water. On the contrary, Yamato (Y) 791197-109, Y-86032-98, Y-86032-95, Y-791197-115 and Y-82192-55A from the lunar highland exhibiting positive Ce anomaly showed IR absorption due to adsorbed water in some of their minerals. The detected water would be of terrestrial origin, because it was not structurally bound and easy to exchange judging from the spectral band shape. The contrast in concentration of adsorbed water between the lunar highland and the mare basalt is derived from a difference in the density of microfractures in mineral grains. Average concentrations of adsorbed water in the lunar highland meteorites were 3.8 mg/cm3 for pyroxene and olivine, and 1.7 mg/cm3 for plagioclase. This contrast between minerals is noteworthy because it has been known that Ce anomaly of pyroxene and olivine is larger than that of plagioclase both for Antarctic lunar meteorites and some lunar rocks. Furthermore, more adsorbed water was detected for minerals in meteorites that exhibit larger Ce anomaly. The present observations demonstrate that the extent of Ce anomaly correlated with the concentration of adsorbed water, which suggests that active mineral surface resulting in adsorption of water could be a trace of interaction forming Ce anomaly. Terrestrial weathering on Antarctica and REE fractionation on the Moon are discussed for possible origins of the Ce anomaly.  相似文献   

19.
Abstract— Bulk chemical compositions of the shergottite basalts provide important constraints on magma genesis and mantle processes in Mars. Abundances of many major and trace elements in the shergottites covary in 2 distinct groups: Group 1 (Gl) includes mostly highly incompatible elements (e.g., La, Th), and Group 2 (G2) includes mostly moderately incompatible elements (e.g., Ti, Lu, Al, Hf). Covariations of G2 elements (not necessarily linear) are consistent with partitioning between basalt magma and orthopyroxene + olivine. This fractionation represents partial melting to form the shergottites and their crystallization; the restite minerals cannot include aluminous phase(s), phosphate, ilmenite, zircon, or sulfides. Overall, abundances of Gl elements are decoupled from those of G2. In graphing abundances of a Gl element against those of a G2 element, G1/G2 abundance ratios do not appear to be random but are restricted to 4 values. Shergottites with a given G1/G2 value need not have the same crystallization age and need not fall on a single fractionation trajectory involving compatible elements (e.g., Ti versus Fe*). These observations imply that the G1/G2 families were established before basalt formation and suggest metasomatic enrichment of their source region (major carrier of G2 elements) by a component rich in Gl elements. Group 1 elements were efficiently separated from G2 elements very early in Mars' history. Such efficient fractionation is not consistent with simple petrogenesis; it requires multiple fractionations, “complex” petrogenetic processes, or minerals with unusual geochemistry. The behavior of phosphorus in this early fractionation event is inexplicable by normal petrogenetic processes and minerals. Several explanations are possible, including significant compatibility of P in majoritic garnet and the presence of P‐bearing iron metal (or a phosphide phase) in the residual solid assemblage (carrier of G2 elements). If the latter, Mars' mantle is more oxidized now than during the ancient fractionation event.  相似文献   

20.
The titanium contents of lunar mare basalts   总被引：1，自引：0，他引：1  
Abstract— Lunar mare basalt sample data suggest that there is a bimodal distribution of TiO2 concentrations. Using a refined technique for remote determination of TiO2, we find that the maria actually vary continuously from low to high values. The reason for the discrepancy is that the nine lunar sample return missions were not situated near intermediate basalt regions. Moreover, maria with 2–4 wt% TiO2 are most abundant, and abundance decreases with increasing TiO2. Maria surfaces with TiO2 >5 wt% constitute only 20% of the maria. Although impact mixing of basalts with differing Ti concentrations may smear out the distribution and decrease the abundance of high‐Ti basalts, the distribution of basalt Ti contents probably reflects both the relative abundances of ilmenite‐free and ilmenite‐bearing mantle sources. This distribution is consistent with models of the formation of mare source regions as cumulates from the lunar magma ocean.  相似文献   

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