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1.
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   

2.
Lunar breccias preserve the records of geologic processes on the Moon. In this study, we report the occurrence, petrography, mineralogy, and geologic significance of the observed secondary olivine veinlets in lunar feldspathic breccia meteorite Northwest Africa (NWA) 11273. Bulk‐rock composition measurements show that this meteorite is geochemically similar to other lunar highland meteorites. In NWA 11273, five clasts are observed to host veinlets that are dominated by interconnecting olivine mineral grains. The host clasts are mainly composed of mafic minerals (i.e., pyroxene and olivine) and probably sourced from a basaltic lithology. The studied olivine veinlets (~5 to 30 μm in width) are distributed within the mafic mineral host, but do not extend into the adjacent plagioclase. Chemically, these olivine veinlets are Fe‐richer (Fo41.4–51.9), compared with other olivine grains (Fo54.3–83.1) in lithic clasts and matrix of NWA 11273. By analogy with the secondary olivine veinlets observed in meteorites from asteroid Vesta (howardite–eucrite–diogenite group samples) and lunar mare samples, our study suggests that the newly observed olivine veinlets in NWA 11273 are likely formed by secondary deposition from a lunar fluid, rather than by crystallization from a high‐temperature silicate melt. Such fluid could be sulfur‐ and phosphorous‐poor and likely had an endogenic origin on the Moon. The new occurrence of secondary olivine veinlets in breccia NWA 11273 reveals that the fluid mobility and deposition could be a previously underappreciated geological process on the Moon.  相似文献   

3.
Lunar highland region and associated craters are mostly composed of anorthosite. In the present study, we studied the reflectance spectra of terrestrial anorthosites collected from Sittampundi Anorthosites Complex, which is considered as equivalent (simulant) of lunar highland anorthosites. The objective of the study is to interpret diagnostic spectral features of analog anorthosite for remotely exploring lunar highland region. Reflectance spectra of anorthosites were measured under two different environments, such as controlled field and laboratory conditions. In these two procedures, the laboratory spectra give clear, diagnostic spectral information in the present study. Reflectance spectra captured under 350-2500 nm covering UV, Visible, NIR, and SWIR part of the electromagnetic spectrum. The spectral characteristics of anorthosites measured under various parts of electromagnetic spectrum have diagnostic absorption features at 380-387, 700-740, 930-1100, 1160-1200, 1415, 1920, 2200 and 2330 nm correspondingly due to plagioclase UV absorption, Fe3+ electron transition absorption, Fe2+ pyroxene and olivine absorption, OH/Mn3+ crystal transition absorption, pyroxene absorption, Al-OH absorption and Mg-OH absorption. Mineralogical and chemical analyses were carried out for four anorthosites and compared with the results of chemical component of lunar anorthosite. The percentage of plagioclase content, relative abundance of low and high calcium pyroxene and olivine in different anorthosite samples are correlated with the albedo range, absorption shape, absorption centers and band depth. The similarity in the diagnostic spectral features of the anolog anorthosite with lunar anorthosites could be effectively utilized for remotely mapping the lunar highland region.  相似文献   

4.
Z.C. Ling  Alian Wang 《Icarus》2011,211(1):101-113
Laser Raman spectroscopy is used to investigate four lunar soils, focusing on mineralogy of grains of <45 μm size. Apollo samples 14163, 15271, 67511, and 71501 were selected as endmembers to study, based on their soil chemistry, maturity, and sample locations. Typical Raman spectral features for major and minor lunar minerals are discussed on the basis of major vibrational modes. We used the Raman peak shift to calculate Mg/(Mg + Fe + Ca) and Ca/(Mg + Fe + Ca) for pyroxene and Mg/(Mg + Fe) for olivine, and thus obtained the compositional distributions of these two minerals in each of the four lunar soils. Classification of feldspar grains was made based on recognition of their Raman patterns. A Raman point-counting procedure was applied to derive mineral modes of the soils, and these are found to be consistent with published modal analysis of these soils. The compositional distributions of pyroxene and olivine grains in each soil sample, as well as the mineral modes, reflect characteristics of the main source materials for these soils. Raman patterns and peak positions also reflect shock effects on plagioclase and quartz, found in 14163.  相似文献   

5.
Faint absorption bands in the visible range of the smoothed vestoid spectra have been found. The bands centered near 505, 530, and 550 nm are attributed to ferrous iron in low-calcium pyroxene and are typical for pyroxene-bearing vestoid surfaces. In accordance with characteristics of the faint absorption bands around 600 and 650 nm the studied vestoid spectra can be sorted into five types. Since the same absorptions are also seen in the laboratory spectra of the minerals and meteorites, which appear to be similar to vestoid material, spectral types of the vestoids can be related to their surface compositions. Regolith of the Type-I vestoids consists of pure low-calcium pyroxenes. Minor amount of olivine along with pyroxene appear to be on the Type-II vestoids whereas the mixtures of low-calcium pyroxene with minor chromite define the Type-III and -IV. The causes for the fifth spectral type in terms of minor mineral phases are unclear now. Simulation of the spectra of vestoids was employed to estimate content of olivine (∼6-12 vol%) and chromite (∼12-30 vol%) on their surfaces.  相似文献   

6.
Measurements have been made of the polarized absorption spectra (360-2200 nm.) of compositionally zoned pyroxene minerals in rocks 10045, 10047 and 10058 and olivines in rocks 10020 and 10022. Specimens in the form of petrographic thin sections were mounted on polarizing microscopes equipped with three-axis universal stage attachments and inserted into a Cary 17 spectrophotometer. The Apollo 11 pyroxenes with relatively high Ti/Fe ratios were chosen initially to investigate the presence of crystal field spectra of Fe2+ and Ti3+ ions in the minerals.Broad intense bands at about 1000 and 2100 nm. arise from spin-allowed, polarization-dependent transitions in Fe2+ ions in pyroxenes. Several weak sharp peaks occur in the visible region. Peaks at 402, 425, 505, 550 and 585 nm. represent spin-forbidden transitions in Fe2+ ions, while broader bands at 460–470 nm. and 650–660 nm. are attributed to Ti3+ ions. Charge transfer bands, which in terrestrial pyroxenes often extend into the visible region, are displaced to shorter wavelengths in lunar pyroxenes. This feature correlates with the absence of Fe3+ ions in these minerals. The magnitudes of the intensity ratios: band 465 nm. (Ti3+) to band 1000 nm. (Fe2+) are similar to Ti/Fe ratios from lunar pyroxene bulk chemical analyses, suggesting that an appreciable amount of titanium occurs as Ti3+ ions in the lunar pyroxenes. The 505 nm. spin-forbidden peak in Fe2+, together with absorption at 465 nm. by Ti3+, contribute to the pink or pale reddish-brown colors of lunar pyroxenes in transmitted lights.The absorption spectral measurements not only provide information on the redox behavior and crystal chemistry of lunar pyroxenes, but also form a basis for interpreting spectral reflectivity properties of lunar rocks and the Moon's surface.  相似文献   

7.
Abstract— Modal mineralogies of individual, equilibrated (petrologic type 4–6 L and LL chondrites have been measured using an electron microprobe mapping technique, and the chemical compositions of coexisting silicate minerals have been analyzed. Progressive changes in the relative abundances and in the molar Fe/Mn and Fe/Mg ratios of olivine, low‐Ca pyroxene, and diopside occur with increasing metamorphic grade. Variations in olivine/low‐Ca pyroxene ratios (Ol/Px) and in metal abundances and compositions with petrologic type support the hypothesis that oxidation of metallic iron accompanied thermal metamorphism in ordinary chondrites. Modal Ol/Px ratios are systematically lower than normative Ol/Px ratios for the same meteorites, suggesting that the commonly used C.I.P.W. norm calculation procedure may not adequately estimate silicate mineral abundances in reduced chondrites. Ol/Px ratios calculated from visible and near‐infrared (VISNIR) reflectance spectra of the same meteorites are not in agreement with other Ol/Px determinations, possibly because of spectral complexities arising from other minerals in chondrites. Characteristic features in VISNIR spectra are sensitive to the proportions and compositions of olivine and pyroxenes, the minerals most affected by oxidative metamorphism. This work may allow spectral calibration for the determination of mineralogy and petrologic type, and thus may be useful for spectroscopic studies of asteroids.  相似文献   

8.
Except for asteroid sample return missions, measurements of the spectral properties of both meteorites and asteroids offer the best possibility of linking meteorite groups with their parent asteroid(s). Visible plus near‐infrared spectra reveal distinguishing absorption features controlled mainly by the Fe2+ contents and modal abundances of olivine and pyroxene. Meteorite samples provide relationships between spectra and mineralogy. These relationships are useful for estimating the olivine and pyroxene mineralogy of stony (S‐type) asteroid surfaces. Using a suite of 10 samples of the acapulcoite–lodranite clan (ALC), we have developed new correlations between spectral parameters and mafic mineral compositions for partially melted asteroids. A well‐defined relationship exists between Band II center and ferrosilite (Fs) content of orthopyroxene. Furthermore, because Fs in orthopyroxene and fayalite (Fa) content in olivine are well correlated in these meteorites, the derived Fs content can be used to estimate Fa of the coexisting olivine. We derive new equations for determining the mafic silicate compositions of partially melted S‐type asteroid parent bodies. Stony meteorite spectra have previously been used to delineate meteorite analog spectral zones in Band I versus band area ratio (BAR) parameter space for the establishment of asteroid–meteorite connections with S‐type asteroids. However, the spectral parameters of the partially melted ALC overlap with those of ordinary (H) chondrites in this parameter space. We find that Band I versus Band II center parameter space reveals a clear distinction between the ALC and the H chondrites. This work allows the distinction of S‐type asteroids as nebular (ordinary chondrites) or geologically processed (primitive achondrites).  相似文献   

9.
The distribution of minerals on the lunar surface is information which could contribute to studying lunar origin and evolution. In this paper, the distribution of clinopyroxene, orthopyroxene, olivine, ilmenite, and plagioclase on the lunar surface has been mapped based on Hapke radiative transfer model and linear unmixing of spectra with Clementine UVVIS/NIR data. The results have been validated on the basis of minerals modal abundance data of the Apollo samples, and problems in the minerals abundance mapping have been analyzed. The validation based on analysis data of Apollo samples indicates that plagioclase mapped in this paper represents the total abundance of plagioclase and agglutinitic glass. The minerals mapping results show that the lunar surface is mainly composed of pyroxene, plagioclase, agglutinitic glass, and ilmenite. Basalt in the lunar mare is mainly composed of clinopyroxene and ilmenite, and lunar highland is mainly composed of plagioclase and agglutinitic glass. Orthopyroxene is mainly distributed on the north of Mare Imbrium, on the south of Maria and Aitken Basin. According to our results, there is probably no large area of olivine distribution on the lunar surface which is different from earlier published results. Therefore, emphasis should be put on the olivine distribution in the minerals mapping using hyperspectral data such as M3 of Chandrayaan-1 and IIM of ChangE-1.  相似文献   

10.
High‐precision oxygen three‐isotope ratios were measured for four mineral phases (olivine, low‐Ca and high‐Ca pyroxene, and plagioclase) in equilibrated ordinary chondrites (EOCs) using a secondary ion mass spectrometer. Eleven EOCs were studied that cover all groups (H, L, LL) and petrologic types (4, 5, 6), including S1–S4 shock stages, as well as unbrecciated and brecciated meteorites. SIMS analyses of multiple minerals were made in close proximity (mostly <100 μm) from several areas in each meteorite thin section, to evaluate isotope exchange among minerals. Oxygen isotope ratios in each mineral become more homogenized as petrologic type increases with the notable exception of brecciated samples. In type 4 chondrites, oxygen isotope ratios of olivine and low‐Ca pyroxene are heterogeneous in both δ18O and Δ17O, showing similar systematics to those in type 3 chondrites. In type 5 and 6 chondrites, oxygen isotope ratios of the four mineral phases plot along mass‐dependent fractionation lines that are consistent with the bulk average Δ17O of each chondrite group. The δ18O of three minerals, low‐Ca and high‐Ca pyroxene and plagioclase, are consistent with equilibrium fractionation at temperatures of 700–1000 °C. In most cases the δ18O values of olivine are higher than those expected from pyroxene and plagioclase, suggesting partial retention of premetamorphic values due to slower oxygen isotope diffusion in olivine than pyroxene during thermal metamorphism in ordinary chondrite parent bodies.  相似文献   

11.
Abstract— Mineralogy, major element compositions of minerals, and elemental and oxygen isotopic compositions of the whole rock attest to a lunar origin of the meteorite Northwest Africa (NWA) 032, an unbrecciated basalt found in October 1999. The rock consists predominantly of olivine, pyroxene and chromite phenocrysts, set in a crystalline groundmass of feldspar, pyroxene, ilmenite, troilite and trace metal. Whole‐rock shock veins comprise a minor, but ubiquitous portion of the rock. Undulatory to mosaic extinction in olivine and pyroxene phenocrysts and micro‐faults in groundmass and phenocrysts also are attributed to shock. Several geochemical signatures taken together indicate unambiguously that NWA 032 originated from the Moon. The most diagnostic criteria include whole‐rock oxygen isotopic composition and ratios of Fe/Mn in the whole rock, olivine, and pyroxene. A lunar origin is documented further by the presence of Fe‐metal, troilite, and ilmenite; zoning to extremely Fe‐rich compositions in pyroxene; the ferrous oxidation state of all Fe in pyroxene; and the rare earth element (REE) pattern with a well‐defined negative europium anomaly. This rock is similar in major element chemistry to basalts from Apollo 12 and 15, but is enriched in light REE and has an unusually high Th/Sm ratio. Some Apollo 14 basalts yield a closer match to NWA 032 in REE patterns, but have higher concentrations of Al2O3. Ar‐Ar step release results are complex, but yield a whole‐rock age of ?2.8 Ga, suggesting that NWA 032 was extruded at 2.8 Ga or earlier. This rock may be the youngest sample of mare basalt collected to date. Noble gas concentrations combined with previously collected radionuclide data indicate that the meteorite exposure history is distinct from currently recognized lunar meteorites. In short, the geochemical and petrographic features of NWA 032 are not matched by Apollo or Luna samples, nor by previously identified lunar meteorites, indicating that it originates from a previously unsampled mare deposit. Detailed assessment of petrographic features, olivine zoning, and thermodynamic modelling indicate a relatively simple cooling and crystallization history for NWA 032. Chromite‐spinel, olivine, and pyroxene crystallized as phenocrysts while the magma cooled no faster than 2 °C/h based on the polyhedral morphology of olivine. Comparison of olivine size with crystal growth rates and preserved Fe‐Mg diffusion profiles in olivine phenocrysts suggest that olivine was immersed in the melt for no more than 40 days. Plumose textures in groundmass pyroxene, feldspar, and ilmenite, and Fe‐rich rims on the phenocrysts formed during rapid crystallization (cooling rates ?20 to 60 °C/h) after eruption.  相似文献   

12.
Among the many ungrouped meteorites, Acfer 370, NWA 7135, and El Médano 301—probably along with the chondritic inclusion in Cumberland Falls and ALHA 78113—represent a homogeneous grouplet of strongly reduced forsterite‐rich chondrites characterized by common textural, chemical, mineralogical, and isotopic features. All of these meteorites are much more reduced than OCs, with a low iron content in olivine and low‐Ca pyroxene. In particular, Acfer 370 is a type 4 chondrite that has olivine and low‐Ca pyroxene compositional ranges of Fa 5.2–5.8 and Fs 9.4–33.4, respectively. The dominant phase is low‐Ca pyroxene (36.3 vol%), followed by Fe‐Ni metal (16.3 vol%) and olivine (15.5 vol%); nevertheless, considering the Fe‐oxyhydroxide (due to terrestrial weathering), the original metal content was around 29.6 vol%. Finally, the mean oxygen isotopic composition Δ17O = +0.68‰ along with the occurrence of a silica phase, troilite, Ni‐rich phosphides, chromite, and oldhamite confirms that these ungrouped meteorites have been affected by strong reduction and are different from any other group recognized so far.  相似文献   

13.
We reexamine the relationship between pyroxene composition and near‐infrared absorption bands, integrating measurements of diverse natural and synthetic samples. We test an algorithm (PLC) involving a two‐part linear continuum removal and parabolic fits to the 1 and 2 μm bands—a computationally simple approach which can easily be automated and applied to remote sensing data. Employing a suite of synthetic pure pyroxenes, the PLC technique is shown to derive similar band centers to the modified Gaussian model. PLC analyses are extended to natural pyroxene‐bearing materials, including (1) bulk lunar basalts and pyroxene separates, (2) diverse lunar soils, and (3) HED meteorites. For natural pyroxenes, the relationship between composition and absorption band center differs from that of synthetic pyroxenes. These differences arise from complexities inherent in natural materials such as exsolution, zoning, mixing, and space weathering. For these reasons, band center measurements of natural pyroxene‐bearing materials are compositionally nonunique and could represent three distinct scenarios (1) pyroxene with a narrow compositional range, (2) complexly zoned pyroxene grains, or (3) a mixture of multiple pyroxene (or nonpyroxene) components. Therefore, a universal quantitative relationship between band centers and pyroxene composition cannot be uniquely derived for natural pyroxene‐bearing materials without additional geologic context. Nevertheless, useful relative relationships between composition and band center persist in most cases. These relationships are used to interpret M3 data from the Humboldtianum Basin. Four distinct compositional units are identified (1) Mare Humboldtianum basalts, (2) distinct outer basalts, (3) low‐Ca pyroxene‐bearing materials, and (4) feldspathic materials.  相似文献   

14.
Here, the petrological features of numerous primitive achondrites and highly equilibrated chondrites are evaluated to review and expand upon our knowledge of the chondrite–achondrite transition, and primitive achondrites in general. A thermodynamic model for the initial silicate melting temperature and progressive melting for nearly the entire known range of oxidation states is provided, which can be expressed as Tm = 0.035Fa2?3.51Fa + 1109 (in °C, where Fa is the proportion of fayalite in olivine). This model is then used to frame a discussion of textural and mineralogical evolution of stony meteorites with increasing temperature. We suggest that the metamorphic petrology of these meteorites should be based on diffusive equilibration among the silicate minerals, and as such, the chondrite–achondrite transition should be defined by the initial point of silicate melting, not by metal–troilite melting. Evidence of silicate melting is preserved by a distinctive texture of interconnected interstitial plagioclase ± pyroxene networks among rounded olivine and/or pyroxene (depending on ?O2), which pseudomorph the former silicate melt network. Indirectly, the presence of exsolution lamellae in augite in slowly cooled achondrites also implies that silicate melting occurred because of the high temperatures required, and because silicate melt enhances diffusion. A metamorphic facies series is defined: the Plagioclase Facies is equivalent to petrologic types 5 and 6, the Sub‐calcic Augite Facies is bounded at lower temperatures by the initiation of silicate melting and at higher temperatures by the appearance of pigeonite, which marks the transition to the Pigeonite Facies.  相似文献   

15.
Abstract— We present combined multi‐spectral imager (MSI) (0.95 μm) and near‐infrared spectrometer (NIS) (0.8–2.4 μm) observations of Psyche crater on S‐type asteroid 433 Eros obtained by the Near‐Earth Asteroid Rendezvous (NEAR)—Shoemaker spacecraft. At 5.3 km in diameter, Psyche is one of the largest craters on Eros which exhibit distinctive brightness patterns consistent with downslope motion of dark regolith material overlying a substrate of brighter material. At spatial scales of 620 m/ spectrum, Psyche crater wall materials exhibit albedo contrasts of 32–40% at 0.946 μm. Associated spectral variations occur at a much lower level of 4–8% (±2–4%). We report results of scattering model and lunar analogy investigations into several possible causes for these albedo and spectral trends: grain size differences, olivine, pyroxene, and troilite variations, and optical surface maturation. We find that the albedo contrasts in Psyche crater are not consistent with a cause due solely to variations in grain size, olivine, pyroxene or lunar‐like optical maturation. A grain size change sufficient to explain the observed albedo contrasts would result in strong color variations that are not observed. Olivine and pyroxene variations would produce strong band‐correlated variations that are not observed. A simple lunar‐like optical maturation effect would produce strong reddening that is not observed. The contrasts and associated spectral variation trends are most consistent with a combination of enhanced troilite (a dark spectrally neutral component simulating optical effects of shock) and lunar‐like optical maturation. These results suggest that space weathering processes may affect the spectral properties of Eros materials, causing surface exposures to differ optically from subsurface bedrock. However, there are significant spectral differences between Eros' proposed analog meteorites (ordinary chondrites and/or primitive achondrites), and Eros' freshest exposures of subsurface bright materials. After accounting for all differences in the measurement units of our reflectance comparisons, we have found that the bright materials on Eros have reflectance values at 0.946 μm consistent with meteorites, but spectral continua that are much redder than meteorites from 1.5 to 2.4 μm. Most importantly, we calculate that average Eros surface materials are 30–40% darker than meteorites.  相似文献   

16.
The valences of Ti, V, and Cr in olivine and pyroxene, important indicators of the fO2 of the source region of their host rocks, can be readily measured nondestructively by XANES (X‐ray absorption near edge structure) spectroscopy, but little such work has been done on lunar rocks, and there is some uncertainty regarding the presence of Ti3+ in lunar silicates and the redox state of the lunar mantle. This is the first study involving direct XANES measurement of valences of multivalent cations in lunar rocks. Because high alumina activity facilitates substitution of Ti cations into octahedral rather than tetrahedral sites in pyroxene and Ti3+ only enters octahedral sites, two aluminous basalts from Apollo 14, 14053 and 14072, were studied. Most pyroxene contains little or no detectable Ti3+, but in both samples relatively early, magnesian pyroxene was found that has Ti valences that are not within error of 4; in 14053, this component has an average Ti valence of 3.81 ± 0.06 (i.e., Ti3+/[Ti3+ + Ti4+ = 0.19]). This pyroxene has relatively low atomic Ti/Al ratios (<0.4) due to crystallization before plagioclase, contrary to the long‐held belief that lunar pyroxene with Ti/Al > 0.5 contains Ti3+ and pyroxene with lower ratios does not. Later pyroxene, with lower Mg/Fe and higher Ti/Al ratios, has higher proportions of Ti (all Ti4+) in tetrahedral sites. All pyroxene analyzed contains divalent Cr, ranging from 15 to 30% of the Cr present, and all but one analysis spot contains divalent V, accounting for 0 to 40% (typically 20–30%) of the V present. Three analyses of olivine in 14053 do not show any Ti3+, but Ti valences in 14072 olivine range from 4 down to 3.70 ± 0.10. In 14053 olivine, ~50% of the Cr and 60% of the V are divalent. In 14072 olivine, the divalent percentages are ~20% for Cr and 20–60% for V. These results indicate significant proportions of divalent Cr and V and limited amounts of trivalent Ti in the parental melts, especially when crystal/liquid partitioning preferences are taken into account. These features are consistent with an fO2 closer to IW ? 2 than to IW ? 1. Apollo 15 basalt 15555, analyzed for comparison with A‐14 materials, has olivine with strongly reduced Cr (Cr2+/(Cr2+ + Cr3+) ~0.9). Basalts from different sites may record redox differences between source regions.  相似文献   

17.
Abstract— Near‐Earth asteroid (25143) 1998 SF36 is a planned target for the Japanese MUSES‐C sample return mission. High signal‐to‐noise and relatively high‐resolution (50 Å) visible and near‐infrared spectroscopic measurements obtained during this asteroid's favorable 2001 apparition reveal it to have a red‐sloped S(IV)‐type spectrum with strong 1 and 2 μm absorption bands analogous to those measured for ordinary chondrite meteorites. This red slope, which is the primary spectral difference between (25143) 1998 SF36 and ordinary chondrite meteorites, is well modeled by the spectrum of 0.05% nanophase iron (npFe0) proposed as a weathering mechanism by Pieters et al. (2000). Asteroid 1998 SF36 appears to have a surface composition corresponding to that of ordinary chondrite meteorites and is most similar in spectral characteristics and modeled olivine/pyroxene content to the LL chondrite class.  相似文献   

18.
Heavily shocked meteorites contain various types of high‐pressure polymorphs of major minerals (olivine, pyroxene, feldspar, and quartz) and accessory minerals (chromite and Ca phosphate). These high‐pressure minerals are micron to submicron sized and occur within and in the vicinity of shock‐induced melt veins and melt pockets in chondrites and lunar, howardite–eucrite–diogenite (HED), and Martian meteorites. Their occurrence suggests two types of formation mechanisms (1) solid‐state high‐pressure transformation of the host‐rock minerals into monomineralic polycrystalline aggregates, and (2) crystallization of chondritic or monomineralic melts under high pressure. Based on experimentally determined phase relations, their formation pressures are limited to the pressure range up to ~25 GPa. Textural, crystallographic, and chemical characteristics of high‐pressure minerals provide clues about the impact events of meteorite parent bodies, including their size and mutual collision velocities and about the mineralogy of deep planetary interiors. The aim of this article is to review and summarize the findings on natural high‐pressure minerals in shocked meteorites that have been reported over the past 50 years.  相似文献   

19.
Abstract— A search of active deflation basins near Jal, Lea County, New Mexico resulted in the discovery of two meteorites, Lea County 001 and 002. Lea County 001 has mean olivine and low-Ca pyroxene compositions of Fa19 and Fs17, respectively. These and all other mineralogical and petrological data collected indicate a classification of H5 for this stone. Lea County 002 has mean olivine and low-Ca pyroxene compositions of Fa2 and Fs4, and is unequilibrated. Although it is mineralogically most similar to Kakangari and chondritic clasts within Cumberland Falls, the high modal amount of forsterite makes Lea County a unique type 3 chondrite. Oxygen isotope data for Lea County 002 fall on an 16O-mixing line through those of the enstatite meteorites and IAB irons, a feature shared by Kakangari.  相似文献   

20.
Lithic fragments in LL-group chondrites commonly have poikilitic textures, in part or in whole, where mainly olivine is enclosed by orthopyroxene. Partially poikilitic fragments also have grano-blastic areas and anhedral olivine larger than the olivine enclosed by pyroxene. In analogy to lunar poikilitic rocks and lithic fragments, poikilitic lithic fragments in LL-group chondrites, i.e., meteorites which are highly brecciated due to repeated impacts, are also interpreted as being related to impact events on meteorite parent bodies where melting and reheating of protolith occurred. Compositional characteristics of minerals in certain fragments, such as highly-unequilibrated clinopyroxene (CaO, 14.5 to 17.3 wt %; Al2O3, 6.7%) and relatively high CaO (0.70 to 2.5 wt %) in orthopyroxene in a Ngawi fragment, seem to indicate a melt origin. However, as in the lunar case, it is difficult to decide whether the meteoritic poikilitic textures resulted from complete or partial melting or largely by solid-state recrystallization, although the large olivines that may be relict crystals appear to indicate that at least partial melting was involved. In all probability, all three processes are responsible for the poikilitic textures in chondrites, since temperature regimes produced by impact processes are likely to range widely. These interpretations may also apply to the poikilitic-textured Shaw chondrite, L-group, which may owe its poikilitic texture to impact partial-melting processes while in the parent body regolith.  相似文献   

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