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1.
Abstract— We describe a previously unreported meteorite found in Axtell, Texas, in 1943. Based on the mineralogical composition and texture of its matrix and the sizes and abundance of chondrules, we classify it as a CV3 carbonaceous chondrite. The dominant opaque phase in the chondrules is magnetite, and that in refractory inclusions is Ni-rich NiFe metal (awaruite). Axtell, therefore, belongs to the oxidized subgroup of CV3 chondrites, although unlike Allende it escaped strong sulfidation. The meteorite bears a strong textural resemblance to Allende, and its chondrule population and matrix appear to be quite similar to those of Allende, but its refractory inclusions, thermoluminescence properties, and cosmogenic 60Co abundances are not. Our data are consistent with a terrestrial age for Axtell of ～100 years and a metamorphic grade slightly lower than that of Allende.  相似文献   

2.
Abstract— This paper describes the use of matrix‐assisted laser desorption and ionization (MALDI) to measure the mass distribution of nanodiamonds extracted from meteorites. The techniques used to prepare and mass analyze nanodiamond samples from the Murchison (CM2) and Allende (CV3) meteorites are described. The mass spectra of nanodiamonds (peaking at between 1 times 104‐1.5 times 104 Daltons) are compared with size distributions obtained by point‐counting transmission electron microscopy (TEM) images obtained elsewhere and reasonable agreement is found. The implications of the ability to produce and mass analyze a beam of nanodiamonds are explored.  相似文献   

3.
Abstract— We have studied Pb‐isotope systematics of chondrules from the oxidized CV3 carbonaceous chondrite Allende. The chondrules contain variably radiogenic Pb with a 206Pb/204Pb ratio between 19.5–268. Pb‐Pb isochron regression for eight most radiogenic analyses yielded the date of 4566.2 ± 2.5 Ma. Internal residue‐leachate isochrons for eight chondrule fractions yielded consistent dates with a weighted average of 4566.6 ± 1.0 Ma, our best estimate for an average age of Allende chondrule formation. This Pb‐Pb age is consistent with the range of model 26Al‐26Mg ages of bulk Allende chondrules reported by Bizzarro et al. (2004) and is indistinguishable from Pb‐Pb ages of Ca‐Al‐rich inclusions (CAIs) from CV chondrites (4567.2 ± 0.6 Ma) (Amelin et al. 2002) and the oldest basaltic meteorites. We infer that chondrule formation started contemporaneously with or shortly after formation of CV CAIs and overlapped in time with formation of the basaltic crust and iron cores of differentiated asteroids. The entire period of chondrule formation lasted from 4566.6 ± 1.0 Ma (Allende) to 4564.7 ± 0.6 Ma (CR chondrite Acfer 059) to 4562.7 ± 0.5 Ma (CB chondrite Gujba) and was either continuous or consisted of at least three discrete episodes. Since chondrules in CB chondrites appear to have formed from a vapor‐melt plume produced by a giant impact between planetary embryos after dust in the protoplanetary disk had largely dissipated (Krot et al. 2005), there were possibly a variety of processes in the early solar system occurring over at least 4–5 Myr that we now combine under the umbrella name of “chondrule formation.”  相似文献   

4.
The analysis of water‐soluble organic compounds in meteorites provides valuable insights into the prebiotic synthesis of organic matter and the processes that occurred during the formation of the solar system. We investigated the concentration of aliphatic monoamines present in hot acid water extracts of the unaltered Antarctic carbonaceous chondrites, Dominion Range (DOM) 08006 (CO3) and Miller Range (MIL) 05013 (CO3), and the thermally altered meteorites, Allende (CV3), LAP 02206 (CV3), GRA 06101 (CV3), Allan Hills (ALH) 85002 (CK4), and EET 92002 (CK5). We have also reviewed and assessed the petrologic characteristics of the meteorites studied here to evaluate the effects of asteroidal processing on the abundance and molecular distributions of monoamines. The CO3, CV3, CK4, and CK5 meteorites studied here contain total concentrations of amines ranging from 1.2 to 4.0 nmol g?1 of meteorite; these amounts are 1–3 orders of magnitude below those observed in carbonaceous chondrites from the CI, CM, and CR groups. The low‐amine abundances for CV and CK chondrites may be related to their extensive degree of thermal metamorphism and/or to their low original amine content. Although the CO3 meteorites, DOM 08006 and MIL 05013, do not show signs of thermal and aqueous alteration, their monoamine contents are comparable to those observed in moderately/extensively thermally altered CV3, CK4, and CK5 carbonaceous chondrites. The low content of monoamines in pristine CO carbonaceous chondrites suggests that the initial amounts, and not asteroidal processes, play a dominant role in the content of monoamines in carbonaceous chondrites. The primary monoamines, methylamine, ethylamine, and n‐propylamine constitute the most abundant amines in the CO3, CV3, CK4, and CK5 meteorites studied here. Contrary to the predominance of n‐ω‐amino acid isomers in CO3 and thermally altered meteorites, there appears to be no preference for the larger n‐amines.  相似文献   

5.
Tibooburra, a new meteorite find from western New South Wales, belongs to the Vigarano subgroup of the carbonaceous chondrites and, on the basis of its opaque mineralogy, appears to be oxidised. Petrological evidence suggests that, like the Allende meteorite, Tibooburra is a CV3 chondrite which has experienced greater metamorphic effects than other CV3 meteorites. Tibooburra has a bulk composition intermediate between the CO and less altered CV chondrites. This transitional nature is exhibited by several elements and is convincingly displayed by the multivariate techniques of cluster analysis and principal component analysis. Tibooburra thus resembles several other CV chondrites, such as Coolidge and Karoonda, which have been strongly metamorphosed. This group of meteorites is believed to have accreted early in the history of the Vigarano parent body and, as a result, contain greater quantities of high temperature Ca-Al-rich inclusions but less low temperature matrix and volatile phases than other CV chondrites. Furthermore, in these meteorites both the matrix and magnesium silicate phases appear to be more iron rich than those in later accreted meteorites. Subsequently, these deeper seated meteorites have undergone more pronounced thermal metamorphism than those located in shallower portions of the parent body.  相似文献   

6.
MgAl2O4 spinels from Allende and NWA 763 carbonaceous chondrites were studied by X‐ray single crystal diffraction, SEM, electron microprobe, LA‐ICP‐MS, and Raman spectroscopy. Those from Allende are almost pure, but, in one case, we found a strong FeOtot zonation. Spinels from NWA 763 show Mg‐Fe2+ substitutions. Almost pure MgAl2O4 spinels from both meteorites underwent slow cooling and reached their intracrystalline closure temperature (Tc) in the range 460–520 °C. The NWA 763 spinel with higher FeO content shows a Tc of about 720 °C. X‐ray single crystal diffraction and Raman spectroscopy suggest a slow cooling and an ordered structure with trivalent cations in M site and divalent in T site. Among the trace elements, Ti and Co are enriched with respect to the terrestrial analogs, while Mn, Ni, and Sn show intermediate values between different terrestrial occurrences. Vanadium cannot be used as a tracer of extraterrestrial origin as for Cr‐spinels, because its content is similar in extraterrestrial and terrestrial spinels. In the zoned crystal from Allende, Co show a strong zonation similar to that of FeO.  相似文献   

7.
Abstract— In order to elucidate the formation of low‐H kaersutites in Martian meteorites, the Fe3+/ΣFe ratio of Chassigny kaersutites in magmatic inclusions was directly determined by the synchrotron microXANES analysis. XANES analysis for standard kaersutites with known Fe3+/ΣFe ratios shows a linear relationship between centroid energy positions of XANES pre‐edge spectra and the Fe3+/ΣFe ratio. Based on the linear relationship, the Fe3+/ΣFe ratio of Chassigny kaersutites is estimated to be about 0.05. The low Fe3+/ΣFe ratio clearly suggests that low‐H kaersutites in Chassigny are not likely to be formed by the oxidation‐dehydrogenation reactions. The low‐H content of the Chassigny kaersutites is mainly due to the presence of a Ti oxy‐component.  相似文献   

8.
187Re‐187Os systematics, abundances of highly siderophile elements (HSE: Re, PGE, and Au), chalcogen elements (Te, Se, and S), and some major and minor elements were determined in physically separated components of the Allende (CV3) and Murchison (CM2) carbonaceous chondrites. Substantial differences exist in the absolute and relative abundances of elements in the components, but the similarity of calculated and literature bulk rock abundances of HSE and chalcogens indicate that chemical complementarity exists among the components, with CI chondrite‐like ratios for many elements. Despite subsequent alteration and oxidation, the overall cosmochemical behavior of most moderately to highly siderophile elements during high‐temperature processing has been preserved in components of Allende at the sampling scale of the present study. The 187Re‐187Os systematics and element variations of Allende are less disturbed compared with Murchison, which reflects different degrees of oxidation and alteration of these meteorites. The HSE systematics (with the exception of Au) is controlled by two types of materials: Pd‐depleted condensates and CI chondrite‐like material. Enrichment and heterogeneous distribution of Au among the components is likely the result of hydrothermal alteration. Chalcogen elements are depleted compared with HSE in all components, presumably due to their higher volatility. Small systematic variations of S, Se, and Te in components bear the signature of fractional condensation/partial evaporation and metal–sulfide–silicate partitioning.  相似文献   

9.
Abstract— The induced thermoluminescence (TL) properties of 16 CV and CV-related chondrites, four CK chondrites and Renazzo (CR2) have been measured in order to investigate their metamorphic history. The petrographic, mineralogical and bulk compositional differences among the CV chondrites indicate that the TL sensitivity of the ～130 °C TL peak is reflecting the abundance of ordered feldspar, especially in chondrule mesostasis, which in turn reflects parent-body metamorphism. The TL properties of 18 samples of homogenized Allende powder heated at a variety of times and temperatures, and cathodoluminescence mosaics of Axtell and Coolidge, showed results consistent with this conclusion. Five refractory inclusions from Allende, and separates from those inclusions, were also examined and yielded trends reflecting variations in mineralogy indicative of high peak temperatures (either metamorphic or igneous) and fairly rapid cooling. The CK chondrites are unique among metamorphosed chondrites in showing no detectable induced TL, which is consistent with literature data that suggests very unusual feldspar in these meteorites. Using TL sensitivity and several mineral systems and allowing for the differences in the oxidized and reduced subgroups, the CV and CV-related meteorites can be divided into petrologic types analogous to those of the ordinary and CO type 3 chondrites. Axtell, Kaba, Leoville, Bali, Arch and ALHA81003 are type 3.0–3.1, while ALH84018, Efremovka, Grosnaja, Allende and Vigarano are type 3.2–3.3 and Coolidge and Loongana 001 are type 3.8. Mokoia is probably a breccia with regions ranging in petrologic type from 3.0 to 3.2. Renazzo often plots at the end of the reduced and oxidized CV chondrite trends, even when those trends diverge, suggesting that in many respects it resembles the unmetamorphosed precursors of the CV chondrites. The low-petrographic types and low-TL peak temperatures of all samples, including the CV3.8 chondrites, indicates metamorphism in the stability field of low feldspar (i.e., <800 °C) and a metamorphic history similar to that of the CO chondrites but unlike that of the ordinary chondrites.  相似文献   

10.
The valence of iron has been used in terrestrial studies to trace the hydrolysis of primary silicate rocks. Here, we use a similar approach to characterize the secondary processes, namely thermal metamorphism and aqueous alteration, that have affected carbonaceous chondrites. X‐ray absorption near‐edge structure spectroscopy at the Fe‐K‐edge was performed on a series of 36 CM, 9 CR, 10 CV, and 2 CI chondrites. While previous studies have focused on the relative distribution of Fe0 with respect to oxidized iron (Feox = Fe2+ + Fe3+) or the iron distribution in some specific phases (e.g., Urey–Craig diagram; Urey and Craig 1953), our measurements enable us to assess the fractions of iron in each of its three oxidation states: Fe0, Fe2+, and Fe3+. Among the four carbonaceous chondrites groups studied, a correlation between the iron oxidation index (IOI = [2(Fe2+) + 3(Fe3+)]/[FeTOT]) and the hydrogen content is observed. However, within the CM group, for which a progressive alteration sequence has been defined, a conversion of Fe3+ to Fe2+ is observed with increasing degree of aqueous alteration. This reduction of iron can be explained by an evolution in the mineralogy of the secondary phases. In the case of the few CM chondrites that experienced some thermal metamorphism, in addition to aqueous alteration, a redox memory of the aqueous alteration is present: a significant fraction of Fe3+ is present, together with Fe2+ and sometimes Fe0. From our data set, the CR chondrites show a wider range of IOI from 1.5 to 2.5. In all considered CR chondrites, the three oxidation states of iron coexist. Even in the least‐altered CR chondrites, the fraction of Fe3+ can be high (30% for MET 00426). This observation confirms that oxidized iron has been integrated during formation of fine‐grained amorphous material in the matrix (Le Guillou and Brearley 2014; Le Guillou et al. 2015; Hopp and Vollmer 2018). Last, the IOI of CV chondrites does not reflect the reduced/oxidized classification based on metal and magnetite proportions, but is strongly correlated with petrographic types. The valence of iron in CV chondrites therefore appears to be most closely related to thermal history, rather than aqueous alteration, even if these processes can occur together (Krot et al. 2004; Brearley and Krot 2013).  相似文献   

11.
More than half of the C-type asteroids, the dominant type of asteroid in the outer half of the main-belt, show evidence of hydration in their reflectance spectra. In order to understand the collisional evolution of asteroids and the production of interplanetary dust and to model the infrared signature of small particles in the Solar System it is important to characterize the dust production from primary impact disruption events, and compare the disruption of hydrous and anhydrous targets. We performed a hypervelocity impact disruption experiment on an ∼30 g target of the Murchison CM2 hydrated carbonaceous chondrite meteorite, and compared the results with our previous disruption experiments on anhydrous meteorites including Allende, a CV3 carbonaceous chondrite, and nine ordinary chondrites. Murchison is significantly more friable than the ordinary chondrites or Allende. Nonetheless, on a plot of mass of the largest fragment versus specific impact energy, the Murchison disruption plots within the field of the anhydrous meteorites points, suggesting that Murchison is at least as resistant to impact disruption as the anhydrous meteorites, which require about twice the energy for disruption as terrestrial anhydrous basalt targets. We determined the mass-frequency distribution of the debris from the Murchison disruption over a nine order-of-magnitude mass range, from ∼10−9 g to the mass of the largest fragment produced in the disruption. The cumulative mass-frequency distribution from the Murchison disruption is fit by three power-law segments. For masses >10−2 g the slope is only slightly steeper than that of the corresponding segment from the disruption of most anhydrous meteorites. Over the range from ∼10−6 to 10−2 g the slope is significantly steeper than that for the anhydrous meteorites. For masses <10−6 g the slopes of both the Murchison and the anhydrous meteorites are almost flat. Thus the Murchison disruption significantly over-produced small fragments (10−6-10−3 g) compared to anhydrous meteorite targets. If the Murchison results are representative of hydrous asteroids, the hydrous asteroids may dominate over anhydrous asteroids in the production of interplanetary dust >100 μm in size, the size of micrometeorites recovered from the polar ices, while both types of asteroids might produce comparable amounts of ∼10 μm interplanetary dust. This would explain the puzzle that polar micrometeorites (>100 μm in size) are similar to hydrous meteorites, while the majority of the ∼10 μm interplanetary dust particles are anhydrous.  相似文献   

12.
Abstract— Mössbauer spectra of martian meteorites are currently of great interest due to the Mössbauer spectrometers on the Athena mission MER rovers as well as the European Space Agency Mars Express mission, with its Beagle 2 payload. Also, considerable current effort is being made to understand the oxygen fugacity of martian magmas because of the effect of fO2 on mineral chemistry and crystallization processes. For these 2 reasons, the present study was conceived to acquire room temperature Mössbauer spectra of mineral separates and whole rock samples of 10 SNC meteorites. The results suggest that mineral identification using remote application of this technique will be most useful when the phases present have distinctive parameters arising from Fe in very different coordination polyhedra; for example, pyroxene coexisting with olivine can be discriminated easily, but opx versus cpx cannot. The MER goal of using Mössbauer spectroscopy to quantify the relative amounts of individual mineral species present will be difficult to satisfy if silicates are present because the lack of constraints on wt% FeO contents of individual silicate phases present will make modal calculations impossible. The remote Mössbauer spectroscopy will be most advantageous if the rocks analyzed are predominantly oxides with known stoichiometries, though these phases are not present in the SNCs. As for the detection of martian oxygen fugacity, no evidence exists in the SNC samples studied of a relationship between Fe3+ content and fO2 as calculated by independent methods. Possibly, all of the Fe3+ observed in olivine is the result of dehydrogenation rather than oxidation, and this process may also be the source of all the Fe3+ observed in pyroxene. The observed Fe3+ in pyroxene also likely records an equilibrium between pyroxene and melt at such low fO2 that little or no Fe3+ would be expected.  相似文献   

13.
The size distribution, abundance, and physical and chemical characteristics of chondritic inclusions are key features that define the chondrite groups. We present statistics on the size and abundance of the macroscopic components (inclusions) in the Murchison (CM2) and Allende (CV3) chondrites and measure their general chemical trends using established X‐ray mapping techniques. This study provides a fine‐scale assessment of the two meteorites and a semiquantitative evaluation of the relative abundances of elements and their distribution among meteorite components. Murchison contains 72% matrix and 28% inclusions; Allende contains 57% and 43%, respectively. A broad range of inclusion sizes and relative abundances has been reported for these meteorites, which demonstrates the necessity for a more standardized approach to measuring these characteristics. Nonetheless, the characteristic mean sizes of inclusions in Allende are consistently larger than those in Murchison. We draw two significant conclusions (1) these two meteorites sampled distinct populations of chondrules and refractory inclusions, and (2) complementary Mg/Si ratios between chondrules and matrix are observed in both Murchison and Allende. Both support the idea that chondrules and matrix within each chondrite group originated in single reservoirs of precursors with approximately solar Mg/Si ratios, providing a constraint on astrophysical models of the origin of chondrite parent bodies.  相似文献   

14.
We report on the primary and secondary mineralogies of three coarse-grained igneous calcium-aluminum-rich inclusions (CAIs) (Compact Type A [CTA], Type B [B], and forsterite-bearing type B [FoB]) from the Northwest Africa (NWA) 5343 (CK3.7) and NWA 4964 (CK3.8) carbonaceous chondrites, compare them with the mineralogy of igneous CAIs from the Allende (CV3.6) chondrite, and discuss the nature of the alteration processes that affected the CK and CV CAIs. The primary mineralogy and mineral chemistry of the CK3 CAIs studied are similar to those from Allende; however, primary melilite and anorthite are nearly completely absent. Although the secondary minerals identified in CK CAIs (Al-diopside, andradite, Cl-apatite, clintonite, forsterite, ferroan olivine, Fe,Ni-sulfides, grossular, ilmenite, magnetite, plagioclase, spinel, titanite, and wadalite) occur also in the Allende CAIs, there are several important differences: (i) In addition to melilite and anorthite, which are nearly completely replaced by secondary minerals, the alteration of CK CAIs also affected high-Ti pyroxenes (fassaite and grossmanite) characterized by high Ti3+/Ti4+ ratio and spinel. These pyroxenes are corroded and crosscut by veins of Fe- and Ti-bearing grossular, Fe-bearing Al,Ti-diopside, titanite, and ilmenite. Spinel is corroded by Fe-bearing Al-diopside and grossular. (ii) The secondary mineral assemblages of grossular + monticellite and grossular + wollastonite, commonly observed in the Allende CAIs, are absent; the Fe-bearing grossular + Fe-bearing Al-diopside ± Fe,Mg-spinel, Fe-bearing grossular + Fe,Mg-olivine ± Fe,Mg-spinel, and Ca,Na-plagioclase + Fe-bearing Al-diopside + Fe-bearing grossular assemblages are present instead. These mineral assemblages are often crosscut by veins of Fe-bearing Al-diopside, Fe,Mg-olivine, Fe,Mg-spinel, and Ca,Na-plagioclase. The coarse-grained secondary grossular and Al-diopside often show multilayered chemical zoning with distinct compositional boundaries between the layers; the abundances of Fe and Ti typically increase toward the grain edges. (iv) Sodium-rich secondary minerals, nepheline and sodalite, commonly observed in the peripheral portions of the Allende CAIs, are absent; Ca,Na-plagioclase is present instead. We conclude that coarse-grained igneous CAIs from CK3.7–3.8 s and Allende experienced an open-system multistage metasomatic alteration in the presence of an aqueous solution–infiltration metasomatism. This process resulted in localized mobilization of all major rock-forming elements: Si, Ca, Al, Ti, Mg, Fe, Mn, Na, K, and Cl. The metasomatic alteration of CK CAIs is more advanced and occurred under higher temperature and higher oxygen fugacity than that of the Allende CAIs.  相似文献   

15.
Abstract— Petrographic, compositional, and isotopic characteristics were studied for three calcium‐aluminum‐rich inclusions (CAIs) and four plagioclase‐bearing chondrules (three of them Al‐rich) from the Axtell (CV3) chondrite. All seven objects have analogues in Allende (CV3) and other primitive chondrites, yet Axtell, like most other chondrites, contains a distinctive suite of CAIs and chondrules. In common with Allende CAIs, CAIs in Axtell exhibit initial 26Al/27Al ratios ((26Al/27Al)0) ranging from ～5 × 10?5 to <1.1 × 10?5, and plagioclase‐bearing chondrules have (26Al/27Al)0 ratios of ～3 × 10?6 and lower. One type‐A CAI has the characteristics of a FUN inclusion. The Al‐Mg data imply that the plagioclase‐bearing chondrules began to form >2 Ma after the first CAIs. As in other CV3 chondrites, some objects in Axtell show evidence of isotopic disturbance. Axtell has experienced only mild thermal metamorphism (<600 °C), probably not enough to disturb the Al‐Mg systematics. Its CAIs and chondrules have suffered extensive metasomatism, probably prior to final accretion. These data indicate that CAIs and chondrules in Axtell (and other meteorites) had an extended history of several million years before their incorporation into the Axtell parent body. These long time periods appear to require a mechanism in the early solar system to prevent CAIs and chondrules from falling into the Sun via gas drag for several million years before final accretion. We also examined the compositional relationships among the four plagioclase‐bearing chondrules (two with large anorthite laths and two barred‐olivine chondrules) and between the chondrules and CAIs. Three processes were examined: (1) igneous differentiation, (2) assimilation of a CAI by average nebular material, and (3) evaporation of volatile elements from average nebular material. We find no evidence that igneous differentiation played a role in producing the chondrule compositions, although the barred olivine compositions can be related by addition or subtraction of olivine. Methods (2) and (3) could have produced the composition of one chondrule, AXCH‐1471, but neither process explains the other compositions. Our study indicates that plagioclase‐bearing objects originated through a variety of processes.  相似文献   

16.
Precise triple oxygen isotope compositions of 32 Allende bulk chondrules (ABCs) are determined using laser‐assisted fluorination mass spectrometry. Various chemically characterized chondrule types show ranges in δ18O that vary from ?4.80‰ to +1.10‰ (porphyritic olivine; PO, N = 15), ?3.10‰ to +1.50‰ (porphyritic olivine pyroxene; POP, N = 9), ?3.40‰ to +2.60‰ (barred olivine; BO, N = 4), and ?3.60‰ to +1.30‰ (porphyritic pyroxene; PP, N = 3). Oxygen isotope data of these chondrules yield a regression line referred to as the Allende bulk chondrule line (ABC line, slope = 0.86 ± 0.02). Most of our data fall closer to the primitive chondrule minerals line (PCM line, slope = 0.987 ± 0.013) and the carbonaceous chondrite anhydrous mineral line (CCAM line, slope = 0.94 ± 0.02) than the Allende anhydrous mineral line (AAML, slope = 1.00 ± 0.01) with a maximum δ18O value (+2.60‰) observed in a BO chondrule and a minimum δ18O value (?4.80‰) shown by a PO chondrule. Similarly, these chondrules depict variable ?17O values that range from ?5.65‰ to ?3.25‰ (PO), ?4.60‰ to ?2.80‰ (POP), ?4.95‰ to ?3.00‰ (BO), ?5.30‰ to ?3.20‰ (PP), and ?4.90‰ (CC). A simple model is proposed for the Allende CV3 chondrite with reference to the AAML and PCM line to illustrate the isotopic variations occurred due to the aqueous alteration processes. The estimated temperature ranging from 10 to 130 °C (mean ~60 °C) implies that the secondary mineralization in Allende happened in a warmer and relatively dry environment compared to Murchison. We further propose that thermal metamorphism could have dehydrated the Allende matrix at temperatures between >150 °C and <600 °C.  相似文献   

17.
Martian meteorites, in particular shergottites, contain darkened olivine (so‐called “brown olivine”) whose color is induced by iron nanoparticles formed in olivine during a shock event. The formation process and conditions of brown olivine have been discussed in the Northwest Africa 2737 (NWA 2737) chassignite. However, formation conditions of brown olivine in NWA 2737 cannot be applied to shergottites because NWA 2737 has a different shock history from that of shergottites. Therefore, this study observed brown olivine in the NWA 1950 shergottite and discusses the general formation process and conditions of brown olivine in shergottites. Our observation of NWA 1950 revealed that olivine is heterogeneously darkened between and within grains different from brown olivine in NWA 2737. XANES analysis showed that brown olivine contains small amounts of Fe3+ and TEM/STEM observation revealed that there is no SiO‐rich phase around iron metal nanoparticles. These observations indicate that iron nanoparticles were formed by a disproportionation reaction of olivine (3Fe2+olivine → Fe0metal + 2Fe3+olivine + Volivine, where Volivine means a vacancy in olivine). Some parts of brown olivine show lamellar textures in SEM observation and Raman peaks in addition to those expected for olivine, implying that brown olivine experienced a phase transition (to e.g., ringwoodite). In order to induce heterogeneous darkening, heterogeneous high temperature of about 1500–1700 K and shock duration of at least ~90 ms are required. This heterogeneous high temperature resulted in high postshock temperature (>900 K) inducing back‐transformation of most high‐pressure phases. Therefore, in spite of lack of high‐pressure phases, NWA 1950 (= Martian meteorites with brown olivine) experienced higher pressure and temperature compared to other highly shocked meteorite groups.  相似文献   

18.
We present results of laboratory near-infrared reflectance studies of a set of calcic pyroxenes with comparable calcium contents (Wo45-50) but variable iron content and oxidation states. This new dataset complements earlier published data (Cloutis and Gaffey, 1991, J. Geophys. Res. 96, 22809-28826, and references therein). In particular, our new spectra extend the scarce available spectral data on chemically analyzed Fe-rich high-Ca clinopyroxenes. We attempted to interpret the spectral behavior of our samples in terms of chemistry and coordination site occupancies. Tentatively, we conclude that Fe-rich calcic pyroxenes have very low contents of Fe2+ in the M2 sites and belong to the spectral type A lacking the 2-μm band. This may be due to high Ca and Mn contents in these pyroxenes. Fe-poor high-Ca pyroxenes are more spectrally variable. In general, they tend to belong to the spectral type B with two major bands near 1 and 2 μm, unless the samples have high Fe3+/Fe2+ ratios or are rich in Mn and Ca. Some of them (including unusual meteorite Angra dos Reis) are of type B despite very high Ca contents. We applied the Modified Gaussian Model (MGM) to characterize three major Fe2+ absorption bands in the 1-μm region of the spectra of Ca-rich pyroxenes. Only the band due to Fe2+ in the M1 coordination site near 1.15 μm may be potentially useful to estimate the Fe content in calcic pyroxenes on remotely-sensed surfaces of Solar System bodies. The spectral variability of basaltic meteorites (angrites) that are rich in calcic pyroxenes is also discussed. The presence of spectral type A calcic pyroxenes in these meteorites complicates unambiguous identification of olivine in asteroid spectra.  相似文献   

19.
Abstract– We report Mg‐Al and Ca‐Ti isotopic data for meteoritic nanodiamonds separated from the Allende CV3 and Murchison CM2 meteorites. The goal of this study was to search for excesses in 26Mg and 44Ca, which can be attributed to the in situ decay of radioactive and now extinct 26Al and 44Ti, respectively. Previous work on presolar SiC and graphite had shown that 26Al/27Al and 44Ti/48Ti ratios in presolar grains can be used to discriminate between different types of stellar sources. Aluminum and Ti concentrations are low in the meteoritic nanodiamonds of this study. Murchison nanodiamonds have higher Al and Ti concentrations than the Allende nanodiamonds. This can be attributed to contamination and the presence of presolar SiC in the Murchison nanodiamond samples. 26Mg/24Mg and 44Ca/40Ca ratios are close to normal in Allende nanodiamonds with upper limits on the initial 26Al/27Al and 44Ti/48Ti ratios of approximately 1 × 10?3. These ratios are factors of 10–1000 and, respectively, 1–1000 lower than those of presolar SiC and graphite grains from supernovae. The 26Al/27Al and 44Ti/48Ti data for nanodiamonds are compatible with an asymptotic giant branch star or solar system origin, but not with a supernova origin of a major fraction of meteoritic nanodiamonds. The latter possibility cannot be excluded, though, as the diamond separates may contain significant amounts of contaminating Al and Ti, which would lower the inferred 26Al/27Al and 44Ti/48Ti ratios considerably.  相似文献   

20.
We report an occurrence of hexagonal CaAl2Si2O8 (dmisteinbergite) in a compact type A calcium‐aluminum‐rich inclusion (CAI) from the CV3 (Vigarano‐like) carbonaceous chondrite Northwest Africa 2086. Dmisteinbergite occurs as approximately 10 μm long and few micrometer‐thick lath‐shaped crystal aggregates in altered parts of the CAI, and is associated with secondary nepheline, sodalite, Ti‐poor Al‐diopside, grossular, and Fe‐rich spinel. Spinel is the only primary CAI mineral that retained its original O‐isotope composition (Δ17O ~ ?24‰); Δ17O values of melilite, perovskite, and Al,Ti‐diopside range from ?3 to ?11‰, suggesting postcrystallization isotope exchange. Dmisteinbergite, anorthite, Ti‐poor Al‐diopside, and ferroan olivine have 16O‐poor compositions (Δ17O ~ ?3‰). We infer that dmisteinbergite, together with the other secondary minerals, formed by replacement of melilite as a result of fluid‐assisted thermal metamorphism experienced by the CV chondrite parent asteroid. Based on the textural appearance of dmisteinbergite in NWA 2086 and petrographic observations of altered CAIs from the Allende meteorite, we suggest that dmisteinbergite is a common secondary mineral in CAIs from the oxidized Allende‐like CV3 chondrites that has been previously misidentified as a secondary anorthite.  相似文献   

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