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1.
Abstract– Fragments of magnesian anorthositic granulite are found in the lunar highlands meteorites Allan Hills (ALH) A81005 and Dhofar (Dho) 309. Five analyzed clasts of meteoritic magnesian anorthositic granulite have Mg′ [molar Mg/(Mg + Fe)] = 81–87; FeO ≈ 5% wt; Al2O3 ≈ 22% wt; rare earth elements abundances ≈ 0.5–2 × CI (except Eu ≈ 10 × CI); and low Ni and Co in a non‐chondritic ratio. The clasts have nearly identical chemical compositions, even though their host meteorites formed at different places on the Moon. These magnesian anorthositic granulites are distinct from other highlands materials in their unique combination of mineral proportions, Mg′, REE abundances and patterns, Ti/Sm ratio, and Sc/Sm ratio. Their Mg′ is too high for a close relationship to ferroan anorthosites, or to have formed as flotation cumulates from the lunar magma ocean. Compositions of these magnesian anorthositic granulites cannot be modeled as mixtures of, or fractionates from, known lunar rocks. However, compositions of lunar highlands meteorites can be represented as mixtures of magnesian anorthositic granulite, ferroan anorthosite, mare basalt, and KREEP. Meteoritic magnesian anorthositic granulite is a good candidate for the magnesian highlands component inferred from Apollo highland impactites: magnesian, feldspathic, and REE‐poor. Bulk compositions of meteorite magnesian anorthositic granulites are comparable to those inferred for parts of the lunar farside (the Feldspathic Highlands Terrane): ～4.5 wt% FeO; ～28 wt% Al2O3; and Th <1 ppm. Thus, magnesian anorthositic granulite may be a widespread and abundant component of the lunar highlands.  相似文献   

2.
The variations of the bulk composition of the silicate Moon (crust + mantle = Bulk Silicate Moon, BSM) depending on the thermal state are explored based on the joint inversion of gravitational, seismic, and petrologic data within the Na2O–TiO2–CaO–FeO–MgO–Al2O3–SiO2 system. The mantle bulk temperature Tmean determining the mineral composition and physical properties of the Moon is adopted as the integral characteristic of thermal state. By parameter Tmean, all thermal models of the Moon can be conventionally broken down into the “cold” with Tmean ~ 690–860°C and the “hot” with Tmean ~ 925–1075°C. The estimations of refractory oxide abundance in lunar rocks depending on the thermal state are included in two different groups. Cold models of BSM are comparable by the bulk content of Al2O3 ~ 3.0–4.6 wt % to those for the silicate Earth (Bulk Silicate Earth, BSE), while hot models of BSM are significantly enriched with Al2O3 ~ 5.1–7.3 wt % (Al2O3 ~ 1.2–1.7 × BSE) as compared with BSE. On the contrary, independent of the temperature distribution, both types of BSM models are characterized by nearly constant values of bulk concentrations of FeO ~ 12–13 wt % and magnesian number MG# 80–81.5 (MG# = [MgO/(MgO + FeO) × 100]), which differ markedly from those for BSE (FeO ~ 8% and MG# 89). It means that for all possible temperature distributions, the silicate fraction of the Moon is FeO-enriched and MgO-depleted in relation to BSE. These arguments discard the possibility of the Moon’s formation out of the material of the Earth’s primitive mantle. In spite of the almost complete coincidence of the isotopic systems, this apparently undeniable fact has no adequate explanation in the existing canonical models of the Moon’s origin and should result in additional constraints on the dynamic processes in models of the formation of the Earth–Moon system. However, the problem of the similarity of and/or difference between compositions of the Moon and the Earth regarding the abundance of refractory elements, which is very important for the geochemistry of the Moon and the Earth’s mantle, remains unresolved and requires further study.  相似文献   

3.
From the Clementine UVVIS imagery of the lunar surface, the abundance of agglutinates in the lunar regolith and their composition in terms of FeO and Al2O3 oxides have been predicted. Data on the spectral, chemical, and mineralogic measurements of about 30 lunar soil samples from the Lunar Samples Characterization Consortium (LSCC) collection were used. The fulfilled prognosis confirms that the mare agglutinates are enriched in Al2O3 and depleted of FeO, while the highland agglutinates are depleted of Al2O3 and enriched in FeO. This behavior can be caused by the global transport of the lunar surface material induced by cosmogenic factors.  相似文献   

4.
Abstract— Darwin glass formed about 800,000 years ago in western Tasmania, Australia. Target rocks at Darwin crater are quartzites and slates (Siluro‐Devonian, Eldon Group). Analyses show 2 groups of glass, Average group 1 is composed of: SiO2 (85%), Al2O3 (7.3%), TiO2 (0.05%), FeO (2.2%), MgO (0.9%), and K2O (1.8%). Group 2 has lower average SiO2 (81.1%) and higher average Al2O3 (8.2%). Group 2 is enriched in FeO (+1.5%), MgO (+1.3%) and Ni, Co, and Cr. Average Ni (416 ppm), Co (31 ppm), and Cr (162 ppm) in group 2 are beyond the range of sedimentary rocks. Glass and target rocks have concordant REE patterns (La/Lu = 5.9–10; Eu/Eu* = 0.55–0.65) and overlapping trace element abundances. 87Sr/86Sr ratios for the glasses (0.80778–0.81605) fall in the range (0.76481–1.1212) defined by the rock samples. ε‐Nd results range from –13.57 to –15.86. Nd model ages range from 1.2–1.9 Ga (CHUR) and the glasses (1.2–1.5 Ga) fall within the range defined by the target samples. The 87Sr/86Sr versus 87Rb/86Sr regression age (411 ± 42 Ma) and initial ratio (0.725 ± 0.016), and the initial 43Nd/144Nd ratio (0.51153 ± 000011) and regression age (451 ± 140 Ma) indicate that the glasses have an inherited isotopic signal from the target rocks at Darwin crater. Mixing models using target rock compositions successfully model the glass for all elementsexcept FeO, MgO, Ni, Co, and Cr in group 2. Mixing models using terrestrial ultramafic rocks fail to match the glass compositions and these enrichments may be related to the projectile.  相似文献   

5.
Abar al' Uj (AaU) 012 is a clast‐rich, vesicular impact‐melt (IM) breccia, composed of lithic and mineral clasts set in a very fine‐grained and well‐crystallized matrix. It is a typical feldspathic lunar meteorite, most likely originating from the lunar farside. Bulk composition (31.0 wt% Al2O3, 3.85 wt% FeO) is close to the mean of feldspathic lunar meteorites and Apollo FAN‐suite rocks. The low concentration of incompatible trace elements (0.39 ppm Th, 0.13 ppm U) reflects the absence of a significant KREEP component. Plagioclase is highly anorthitic with a mean of An96.9Ab3.0Or0.1. Bulk rock Mg# is 63 and molar FeO/MnO is 76. The terrestrial age of the meteorite is 33.4 ± 5.2 kyr. AaU 012 contains a ~1.4 × 1.5 mm2 exotic clast different from the lithic clast population which is dominated by clasts of anorthosite breccias. Bulk composition and presence of relatively large vesicles indicate that the clast was most probably formed by an impact into a precursor having nonmare igneous origin most likely related to the rare alkali‐suite rocks. The IM clast is mainly composed of clinopyroxenes, contains a significant amount of cristobalite (9.0 vol%), and has a microcrystalline mesostasis. Although the clast shows similarities in texture and modal mineral abundances with some Apollo pigeonite basalts, it has lower FeO and higher SiO2 than any mare basalt. It also has higher FeO and lower Al2O3 than rocks from the FAN‐ or Mg‐suite. Its lower Mg# (59) compared to Mg‐suite rocks also excludes a relationship with these types of lunar material.  相似文献   

6.
Abstract— A report is presented for a possible revised classification of lunar igneous rocks that still uses the division of Moon rocks into mare and highland types. It subdivides the mare rocks into basalts depending on TiO2 content and glasses depending on colour, and subdivides the highland rocks principally into KREEP basalts and into coarse‐grained igneous rocks comparable to and using terrestrial igneous rock terminology.  相似文献   

7.
The composition and chemistry of Mercury’s regolith has been calculated from MESSENGER MASCS 0.3-1.3 μm spectra from the first flyby, using an implementation of Hapke’s radiative transfer-based photometric model for light scattering in semi-transparent porous media, and a linear spectral mixing algorithm. We combine this investigation with linear spectral fitting results from mid-infrared spectra and compare derived oxide abundances with mercurian formation models and lunar samples. Hapke modeling results indicate a regolith that is optically dominated by finely comminuted particles with average area weighted grain size near 20 μm. Mercury shows lunar-style space weathering, with maturation-produced microphase iron present at ∼0.065 wt.% abundance, with only small variations between mature and immature sites, the amount of which is unable to explain Mercury’s low brightness relative to the Moon. The average modal mineralogies for the flyby 1 spectra derived from Hapke modeling are 35-70% Na-rich plagioclase or orthoclase, up to 30% Mg-rich clinopyroxene, <5% Mg-rich orthopyroxene, minute olivine, ∼20-45% low-Fe, low-Ti agglutinitic glass, and <10% of one or more lunar-like opaque minerals. Mercurian average oxide abundances derived from Hapke models and mid-infrared linear fitting include 40-50 wt.% SiO2, 10-35 wt.% Al2O3, 1-8 wt.% FeO, and <25 wt.% TiO2; the inferred rock type is basalt. Lunar-like opaques or glasses with high Fe and/or Ti abundances cannot on their own, or in combination, explain Mercury’s low brightness. The linear mixing results indicate the presence of clinopyroxenes that contain up to 21 wt.% MnO and the presence of a Mn-rich hedenbergite. Mn in M1 crystalline lattice sites of hedenbergite suppresses the strong 1 and 2 μm crystal field absorption bands and may thus act as a strong darkening agent on Mercury. Also, one or more of thermally darkened silicates, Fe-poor opaques and matured glasses, or Mercury-unique Ostwald-ripened microphase iron nickel may lower the albedo. A major part of the total microphase iron present in Mercury’s regolith is likely derived from FeO that is not intrinsic to the crust but has been subsequently delivered by exogenic sources.  相似文献   

8.
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   

9.
A principal goal of the Lunar Soil Characterization Consortium (LSCC) is to evaluate tools that might be successfully used in remote compositional analysis of the lunar surface. Mathematical methods are extremely valuable to assess whether variations exist in a statistically significant manner, independent of their interpretation. The bounds of widely used correlation of visible to near-infrared spectral parameters with composition are first defined and evaluated. We then evaluate direct (or indirect) links between the combined spectral properties of lunar mare soils and their compositional properties (elemental abundance and mineralogy) through a statistical analysis of the variance across each measurement using principal component analysis (PCA). We first separately analyze LSCC elemental abundance, mineralogy, and spectroscopy data (0.35 to 2.5 μm) using PCA to capture the variance of each system with a relatively small number of independent variables. With this compact set of independent variables for each type of data, we derive functions to link composition and spectroscopy. For these mare soils, one of the best empirical predictive capability is that for FeO. This is not surprising since the effect of ferrous iron on optical properties is well documented. Although Al2O3 has no direct effect on optical properties, its strong anticorrelation with FeO also produces a relatively high predictive capability from spectra. Similarly, a high accuracy in predicting the abundance of pyroxene is observed and should be expected since iron-bearing pyroxene is one of the most optically active components of lunar soil. The accuracy for predicting either TiO2 or ilmenite, on the other hand, is disappointing. High- and low-Ti soils are readily distinguished, but these statistics suggest that making subclass distinctions based on spectral predictions of TiO2 would be risky.  相似文献   

10.
Abstract— –Sayh al Uhaymir (SaU) 169 is a composite lunar meteorite from Oman that consists of polymict regolith breccia (8.44 ppm Th), adhering to impact‐melt breccia (IMB; 32.7 ppm Th). In this contribution we consider the regolith breccia portion of SaU 169, and demonstrate that it is composed of two generations representing two formation stages, labeled II and III. The regolith breccia also contains the following clasts: Ti‐poor to Ti‐rich basalts, gabbros to granulites, and incorporated regolith breccias. The average SaU 169 regolith breccia bulk composition lies within the range of Apollo 12 and 14 soil and regolith breccias, with the closest correspondence being with that of Apollo 14, but Sc contents indicate a higher portion of mare basalts. This is supported by relations between Sm‐Al2O3, FeO‐Cr2O3‐TiO2, Sm/Eu and Th‐K2O. The composition can best be modeled as a mixture of high‐K KREEP, mare basalt and norite/troctolite, consistent with the rareness of anorthositic rocks. The largest KREEP breccia clast in the regolith is identical in its chemical composition and total REE content to the incompatible trace‐element (ITE)‐ rich high‐K KREEP rocks of the Apollo 14 landing site, pointing to a similar source. In contrast to Apollo 14 soil, SaU 169 IMB and SaU 169 KREEP breccia clast, the SaU 169 regolith is not depleted in K/Th, indicating a low contribution of high‐Th IMB such as the SaU 169 main lithology in the regolith. The data presented here indicate the SaU 169 regolith breccia is from the lunar front side, and has a strong Procellarum KREEP Terrane signature.  相似文献   

11.
This paper presents an updated stratigraphical and compositional study of the exposed maria within the Imbrium basin on the Moon. Clementine multispectral data were employed to derive TiO2 and FeO wt% abundance estimates of potentially distinct basaltic flows. Additionally, NASA Lunar Orbiter images were used to estimate flow ages using crater count statistics. Mare Imbrium shows evidence of a complex suite of low to high-Ti basaltic lava units infilling the basin over an 800 million year timescale. More than a third (37%) of identified mare basalts were found to contain 1-3 wt% TiO2. Two other major mare lithological units (representing about 25% of the surface each) show TiO2 values between 3-5 and 7-9 wt%. The dominant fraction (55%) of the sampled maria contain FeO between 16 and 18 wt%, followed by 27% of maria having 18-20 wt% and the remaining 18%, 14-16 wt% FeO. A crater frequency count (for diameters >500 m) shows that in three quarters of the sampled mare crater counts range between 3.5 and 5.5×10−2 per km2, which translates, according to a lunar cratering model chronology, into estimated emplacement ages between ∼3.3 and 2.5 Ga. A compositional convergence trend between the variations of iron and titanium oxides was identified, in particular for materials with TiO2 and FeO content broadly above 5 and 17 wt%, respectively, suggesting a related petrogenesis and evolution. According to these findings, three major periods of mare infill are exposed in the Imbrium basin; despite each period showing a range of basaltic compositions (classified according to their TiO2 content), it is apparent that, at least within these local geological settings, the igneous petrogenesis generally evolved through time towards more TiO2- and FeO-rich melts.  相似文献   

12.
Niobian rutile was found in a KREEP lithic fragment of basaltic texture. The niobian rutile contains 85.3% TiO2, 7.1% Nb2O5, 2.65% Cr2O3, 0.70% ZrO2, 0.61% SiO2, 0.82% Al2O3 0.61% FeO, 0.52% CaO, 0.22% V2O3 in addition to minor amounts of MnO, MgO, and CeO2. Rare earth elements were not detected, in contrast with lunar niobian rutile of Marvin (1971). Coexisting minerals in the KREEP fragment are major amounts of plagioclase and orthopyroxene, and minor amounts of olivine, ilmenite, augite, barian K-feldspar, whitlockite, troilite, Ni-Fe, zirkelite and chromite  相似文献   

13.
Abstract— Phase equilibrium experiments on the most magnesian Apollo 15C green picritic glass composition indicate a multiple saturation point with olivine and orthopyroxene at 1520°C and 1.3 GPa (about 260 km depth in the moon). This composition has the highest Mg# of any lunar picritic glass and the shallowest multiple saturation point. Experiments on an Apollo 15A composition indicate a multiple saturation point with olivine and orthopyroxene at 1520°C and 2.2 GPa (about 440 km depth in the moon). The importance of the distinctive compositional trends of the Apollo 15 groups A, B, and C picritic glasses merits the reanalysis of NASA slide 15426,72 with modern electron microprobe techniques. We confirm the compositional trends reported by Delano (1979, 1986) in the major element oxides SiO2, TiO2, Al2O3, Cr2O3, FeO, MnO, MgO, and CaO, and we also obtained data for the trace elements P2O5, K2O, Na2O, NiO, S, Cu, Cl, Zn, and F. Petrogenetic modeling demonstrates that the Apollo 15 A‐B‐C glass trends could not have been formed by fractional crystallization or any continuous assimilation/fractional crystallization (AFC) process. The B and C glass compositional trends could not have been formed by batch or incremental melting of an olivine + orthopyroxene source or any other homogeneous source, though the A glasses may have been formed by congruent melting over a small pressure range at depth. The B compositional trend is well modeled by starting with an intermediate A composition and assimilating a shallower, melted cumulate, and the C compositional trend is well modeled by a second assimilation event. The assimilation process envisioned is one in which heat and mass transfer were separated in space and time. In an initial intrusive event, a picritic magma crystallized and provided heat to melt magma ocean cumulates. In a later replenishment event, the picritic magma incrementally mixed with the melted cumulate (creating the compositional trends in the green glass data set), ascended to the lunar surface, and erupted as a fire fountain. A barometer created from multiple saturation points provides a depth estimate of other glasses in the A‐B‐C trend and of the depths of assimilation. This barometer demonstrates that the Apollo 15 A‐B‐C trend originated over a depth range of ?460 km to ?260 km within the moon.  相似文献   

14.
Abstract— The lunar soil characterization consortium, a group of lunar‐sample and remote‐sensing scientists, has undertaken the extensive task of characterization of the finest fractions of lunar soils, with respect to their mineralogical and chemical makeup. These compositional data form the basis for integration and modeling with the reflectance spectra of these same soil fractions. This endeavor is aimed at deciphering the effects of space weathering of soils on airless bodies with quantification of the links between remotely sensed reflectance spectra and composition. A beneficial byproduct is an understanding of the complexities involved in the formation of lunar soil. Several significant findings have been documented in the study of the <45 μm size fractions of selected Apollo 17 mare soils. As grain size decreases, the abundance of agglutinitic glass increases, as does the plagioclase, whereas the other minerals decrease. The composition of the agglutinitic glass is relatively constant for all size fractions, being more feldspathic than any of the bulk compositions; notably, TiO2 is substantially depleted in the agglutinitic glass. However, as grain size decreases, the bulk composition of each size fraction continuously changes, becoming more Al‐rich and Fe‐poor, and approaches the composition of the agglutinitic glasses. Between the smallest grain sizes (10–20 and < 10 μm), the IS/FeO values (amount of total iron present as nanophase Fe0) increase by greater than 100% (>2x), whereas the abundance of agglutinitic glass increases by only 10–15%. This is evidence for a large contribution from surface‐correlated nanophase Fe0 to the IS/FeO values, particularly in the <10 μm size fraction. The surface nanophase Fe0 is present largely as vapor‐deposited patinas on the surfaces of almost every particle of the mature soils, and to a lesser degree for the immature soils (Keller et al., 1999a). It is reasoned that the vapor‐deposited patinas may have far greater effects upon reflectance spectra of mare soils than the agglutinitic Fe0.  相似文献   

15.
Laser-induced breakdown spectroscopy (LIBS) was used to quantitatively analyze 195 rock slab samples with known bulk chemical compositions, 90 pressed-powder samples derived from a subset of those rocks, and 31 pressed-powder geostandards under conditions that simulate the ChemCam instrument on the Mars Science Laboratory Rover (MSL), Curiosity. The low-volatile (<2 wt.%) silicate samples (90 rock slabs, corresponding powders, and 22 geostandards) were split into training, validation, and test sets. The LIBS spectra and chemical compositions of the training set were used with three multivariate methods to predict the chemical compositions of the test set. The methods were partial least squares (PLS), multilayer perceptron artificial neural networks (MLP ANNs) and cascade correlation (CC) ANNs. Both the full LIBS spectrum and the intensity at five pre-selected spectral channels per major element (feature selection) were used as input data for the multivariate calculations. The training spectra were supplied to the algorithms without averaging (i.e. five spectra per target) and with averaging (i.e. all spectra from the same target averaged and treated as one spectrum). In most cases neural networks did not perform better than PLS for our samples. PLS2 without spectral averaging outperformed all other procedures on the basis of lowest quadrature root mean squared error (RMSE) for both the full test set and the igneous rocks test set. The RMSE for PLS2 using the igneous rock slab test set is: 3.07 wt.% SiO2, 0.87 wt.% TiO2, 2.36 wt.% Al2O3, 2.20 wt.% Fe2O3, 0.08 wt.% MnO, 1.74 wt.% MgO, 1.14 wt.% CaO, 0.85 wt.% Na2O, 0.81 wt.% K2O. PLS1 with feature selection and averaging had a higher quadrature RMSE than PLS2, but merits further investigation as a method of reducing data volume and computation time and potentially improving prediction accuracy, particularly for samples that differ significantly from the training set. Precision and accuracy were influenced by the ratio of laser beam diameter (∼490 μm) to grain size, with coarse-grained rocks often resulting in lower accuracy and precision than analyses of fine-grained rocks and powders. The number of analysis spots that were normally required to produce a chemical analysis within one standard deviation of the true bulk composition ranged from ∼10 for fine-grained rocks to >20 for some coarse-grained rocks.  相似文献   

16.
Optical absorption and diffuse reflectance spectra were obtained for simulated lunar glasses of four different compositions, both in their as-quenched (reduced) states and following mild subsolidus oxidation. The transmission spectra, when normalized by the FeO content of the glasses, differed from one another only in the relative intensity of an unresolved band in the UV. For fixed melting conditions the strength of this band in the as-quenched glasses increased with increasing FeO, or with increasing TiO2 for a fixed FeO content. Electron spin resonance (ESR) experiments have demonstrated the absence of Fe3+ or Ti3+ and the presence of metallic iron in these materials; all other transition-group elements were excluded in preparation. The unresolved UV absorption edge in the as-quenched reduced glasses is therefore tentatively ascribed to Fe2+Ti4+ intervalency charge transfer transitions. A similar UV edge was also produced by oxidation, leading to the conclusion that the assignment of this band would be ambiguous in the absence of an independent determination of the valence states of Fe and Ti. The relationship between the transmission spectra of polished samples and the reflectance spectra of sieved powders of the same materials is shown to be well described by the Kubelka-Munk approximation. Using this insight, it is possible to understand the spectral characteristics both of oxidation darkening of synthetic glass powders and of maturation darkening of lunar soils in terms of (1) the growth of the aforementioned charge transfer band(s) and (2) the development of opaque surface phases. It is shown that mechanism (1) is of primary importance in lunar highland materials and that mechanism (2) dominates in mare materials. The present results, coupled with previous findings, suggest that lunar soil maturation darkening may result from vitrification only if accompanied by (a) enrichment in the elements Fe and Ti, (b) changes in valence states of these elements, (c) partial crystallization of opaque phases such as iron, ilmenite or magnetite, or (d) a combination of (a), (b), and (c).  相似文献   

17.
A large number of shock recovery experiments that address the ease of impact melt formation as a function of peak shock pressure lead to the conclusion that impacts at 5 km/sec into fragmental, porous surfaces will produce agglutinate-type glasses; no shock melts are produced at these velocities in dense silicate target rocks. While agglutinitic glasses dominate lunar surface soils, they are virtually absent in gas-rich, brecciated meteorites. This apparent paucity—if not complete lack—of agglutinate-type glasses is also inferred from remote IR-reflectance spectroscopy. The need to identify mechanisms that inhibit agglutinate formation on asteroidal sufaces was recognized previously and was predominantly attributed to lower projectile velocities and different gravitational environments.We will argue in this paper that additional mechanisms may be required. Specifically we propose that spall processes at a target's free surface play a major role in asteroidal surface evolution. At 5 km/sec collision velocity, a target (RT) to projectile (RP radius ratio of RTRP ≈ 100 delineates the boundary between an “infinite half-space” and a “finite”-sized target. In the first case, collisional energy is expended in a pure cratering regime; in the latter, additional displacement of target material in the form of spallation products occurs. The spall volume may exceed the crater volume by an order of magnitude. Therefore fragmental impact deposits on small planetary bodies may be entirely controlled by spall products, rather than crater ejecta. Because tensile failure occurs at <0.2 GPa stress, spall velocities are measured in meters per second (contrary to crater ejecta) and therefore spallation products are efficiently retained even in low gravitational environments. Spall products are also more coarse grained than crater ejecta; they are also highly biased toward petrographically “unshocked” (<0.2 GPa) rocks.Thus asteroidal surface deposits should be more coarse grained and less shocked than lunar ones—consistent with meteorite evidence and remote-sensing observations. Because spall volume exceeds crater ejecta volume, the total growth rate of asteroidal surface deposits is accelerated, leading to relatively short surface residence times of individual meteorite components, another significant difference between lunar and asteroidal surface materials.  相似文献   

18.
The olivine crystals of the 77005 achondrite are brown except for colorless shock lamellae, mottled patches, and grains adjacent to pools of impact melt. Sporadic dark alteration patches in brown olivine and Cr-rich spinel gave the following average electron-microprobe analyses: (olivine) P2O5 0.9, SiO2 57.9, TiO2 0, Al2O3 0.7, Cr2O3 0.4, V2O3 0, Fe2O3 (assumed oxidation state) 17.0, MgO 1.6, CaO 0.2, Na2O 0, K2O 1.8, SO3 (assumed oxidation state) 9.2, Cl 0.1, sum 89.8 wt. %; (spinel) P2O53.5, SiO22.1, TiO2.2.2, Al2O32.1, Cr2O3 13.4, V2O3 0.8, Fe2O3 40.7, MgO 0.9, CaO 0.1, Na2O 0, K2O 2.0, SO3 11.1, Cl 0.1, sum 79.0 wt.%. Ion-microprobe analyses revealed H in both. Rare orange patches in brown olivine from another area gave SiO2 33–35, FeO 30-28, MgO 28–32, sum 93 wt. %. Thermal metamorphism under dry oxidizing conditions is discussed as a possible alternative to shock-induced oxidation for generation of the brown olivine (McSween and Stöffler). Because alteration patches transgress shock lamellae, and because sulfatic alteration occurs in fusion crusts of Antarctic meteorites (Gibson et al., 1983), alteration of the 77005 achondrite at the Antarctic surface is preferred to a complex series of processes needed for pre-terrestrial alteration.  相似文献   

19.
Abstract— We have studied the mare basalts of Mare Humorum and southeastern Procellarum (30°W–50°W, 0°–40°S). One hundred and nine basaltic units have been identified from differences in their FeO wt% and TiO2 wt% content, and variations in crater densities. Crater counting and reference to isotopically dated Apollo samples have provided an age for 33 major units. Some evidence for three distinct periods of volcanic activity has been found. We found that the large unit in the middle of Mare Humorum is the oldest in the basin. This supports the suggestion that the oldest central unit sank causing the lithosphere to bend and create dykes through which lava flowed to produce the outer units. No evidence of a trend in FeO wt% and TiO2 wt% content against time is found within Mare Humorum. There appears to be no lateral trend of basalts in terms of FeO and TiO2 wt% over the entire area with time. An increase in FeO content with time is found in the 33 major units and there is some evidence for an increase in TiO2 in the same units. A correlation between FeO wt% and TiO2 wt% content is evident when all 109 units are compared. A notable feature of this correlation is a sharp increase in gradient of TiO2 wt% content when the FeO wt% content rises above about 17%.  相似文献   

20.
Abstract— The howardite‐eucrite‐diogenite (HED) clan is a group of meteorites that probably originate from the asteroid Vesta. Some of them are complex breccias that contain impact glasses whose compositions mirror that of their source regions. Some K‐rich impact glasses (up to 2 wt% K2O) suggest that in addition to basalts and ultramafic cumulates, K‐rich rocks are exposed on Vesta's surface. One K‐rich glass (up to 6 wt% K2O), with a felsic composition, provides the first evidence of highly differentiated K‐rich rocks on a large asteroid. They can be compared to the rare lunar granites and suggest that magmas generated in a large asteroid are more diverse than previously thought.  相似文献   

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