Infrared spectroscopic taxonomy for carbonaceous chondrites from speciation of hydrous components

Abstract— Mid‐infrared absorption spectra for all types of carbonaceous chondrites were obtained in this study to establish a versatile method for spectroscopic classification of carbonaceous chondrites. Infrared spectra were measured using a conventional KBr pellet method and diamond press method. Spectra of hydrous carbonaceous chondrites exhibit intense O‐H stretching vibrations. CI chondrites are identifiable by a characteristic sharp absorption band appearing at 3685 cm^?1, which is mainly attributable to serpentine. X‐ray diffraction analysis showed the presence of serpentine. However, Yamato (Y‐) 82162 (C1) does not have the band at 3685 cm^?1 because of its thermal metamorphism. CM and CR chondrites have an intense absorption band at approximately 3600 cm^?1. This absorption tends to appear in CM chondrites more strongly than CR chondrites because the intensity ratios of an OH stretching mode at 3520 cm^?1 compared to 3400 cm^?1 for CM chondrites are in the range of 0.95–1.04, which is systematically higher than those of CR chondrites (0.86–0.88). Therefore, the two types of chondrites are distinguishable by their respective infrared spectra. The spectrum feature of the Tagish Lake meteorite is attributable to neither CI nor CM chondrites. CO chondrites are characterized by weak and broad absorption at 3400 cm^?1. CV chondrites have weak or negligible absorption of water. CK chondrites also have no water‐induced absorption. CH and CB chondrites have a sharp absorption at 3692 cm^?1 indicating the presence of chrysotile, which is also supported by observations of X‐ray diffraction and TEM. The combination of spectroscopic classification and the diamond press method allows classification of carbonaceous chondrites of very valuable samples with small quantities. As one example, carbonaceous chondrite clasts in brecciated meteorites were classified using our technique. Infrared spectra for a fragment of carbonaceous clasts (<1 μg) separated from Willard (b) and Tsukuba were measured. The 3685 cm^?1 band found in CI chondrites was clearly detected in the clasts, indicating that they are CI‐like clasts.     

Absorption bands near three micrometers in diffuse reflectance spectra of carbonaceous chondrites: Comparison with asteroids

Abstract— We measured infrared diffuse reflectance spectra of several carbonaceous chondrites in order to obtain additional information on the surface materials of their presumed parent bodies, C-type asteroids. The presence and intensity of absorption bands near 3 μm in the reflectance spectra are due to the presence and abundance of hydrates and/or hydroxyl ions. The absorption features of the 3 μm hydration bands of carbonaceous chondrites were compared with those of asteroids 1 Ceres and 2 Pallas. They are commonly classified into separate subtypes, G- and B-type. The spectral shapes of Pallas and Renazzo (CR2 chondrite) around the 3 μm absorption band are an excellent match. This result may suggest that the amount of hydrous minerals in the surface material of Pallas is smaller than that in the CM2 or CI chondrites, and the hydrous minerals on the surface of Pallas may be similar to those found in Renazzo. The spectral features around the 3 μm band of Ceres are different from those of carbonaceous chondrites studied in this paper.     

Thermal metamorphism of CI and CM carbonaceous chondrites: An internal heating model

Abstract— Infrared diffuse reflectance spectra were measured for several thermally metamorphosed carbonaceous chondrites with CI-CM affinities which were recently found from Antarctica. Compared with other CI or CM carbonaceous chondrites, these Antarctic carbonaceous chondrites show weaker absorption bands near 3 μm due to hydrous minerals, and weaker absorption bands near 6.9 μm due to carbonates, interpreted as thermal metamorphic features. These absorption bands also disappear in the spectra of samples of the Murchison (CM) carbonaceous chondrite heated above 500 °C, implying that the metamorphic temperatures of the Antarctic carbonaceous chondrites considered here were higher than about 500 °C. Model calculations were performed to study thermal metamorphism of carbonaceous chondrites in a parent body internally heated by the decay of the extinct nuclide ²⁶Al. The maximum temperature of the interior of a body more than 20 km in radius is 500–700 °C for the bulk Al contents of CI and CM carbonaceous chondrites, assuming a ratio of ²⁶Al/²⁷Al = 5 × 10^?6 which has been previously proposed for an ordinary-chondrite parent body. The metamorphic temperatures experienced by the Antarctic carbonaceous chondrites considered here may be attainable by an internally heated body with an ²⁶Al/²⁷Al ratio similar to that inferred for an ordinary-chondrite parent body.     

The mid-infrared transmission spectra of Antarctic ureilites

Abstract— The mid-infrared (4000–450 cm^?1; 2.5–22.2 μm) transmission spectra of seven Antarctic ureilites and 10 Antarctic H-5 ordinary chondrites are presented. The ureilite spectra show a number of absorption bands, the strongest of which is a wide, complex feature centered near 1000 cm^?1 (10 μm) due to Si-O stretching vibrations in silicates. The profiles and positions of the substructure in this feature indicate that Mg-rich olivines and pyroxenes are the main silicates responsible. The relative abundances of these two minerals, as inferred from the spectra, show substantial variation from meteorite to meteorite, but generally indicate olivine is the most abundant (olivine:pyroxene = 60:40 to 95:5). Both the predominance of olivine and the variable olivine-to-pyroxene ratio are consistent with the known composition and heterogeneity of ureilites. The H-5 ordinary chondrites spanned a range of weathering classes and were used to provide a means of addressing the extent to which the ureilite spectra may have been altered by weathering processes. It was found that, while weathering of these meteorites produces some weak bands due to the formation of small amounts of carbonates and hydrates, the profile of the main silicate feature has been little affected by Antarctic exposure in the meteorites studied here. The mid-infrared ureilite spectra provide an additional means of testing potential asteroidal parent bodies for the ureilites. At present, the best candidates include the subset of S-type asteroids having low albedos and weak absorption features in the near infrared.     

An investigation of the presence and nature of phyllosilicates on the surfaces of C asteroids by an analysis of the continuum slopes in their near‐infrared spectra

Abstract– To understand the nature of C asteroid surfaces, which are often related to phyllosilicates and C chondrites, we report near‐infrared spectra for a suite of phyllosilicates, heated to 100–1100 °C in 100 °C intervals, and compare the results for telescope IRTF spectra for 11 C asteroids. As C asteroids have relatively featureless spectra, we focus on “continuum plots” (1.0–1.75 μm slope against 1.8–2.5 μm slope). We compare the continuum plots of the 11 C asteroids and our heated phyllosilicates with literature data for C chondrites. The CI, CR, CK, and CV chondrite meteorites plot in the C asteroid field, whereas CM chondrites plot in a close but discrete field. All are well separated from the large phyllosilicate field. Heating kaolinite and montmorillonite to ≥700 °C moves their continua slopes into the C asteroid field, whereas chlorite and serpentine slopes move into the CM chondrite field. Water losses during heating are generally 10–15 wt% and were associated with a 20–70% albedo drop. Our data are consistent with surfaces of the C asteroids consisting of the dehydration products of montmorillonite whereas the CM chondrites are the dehydration products of serpentine and chlorite. The presence of opaque minerals and evaporites does not provide quantitative explanations for the difference in continua slopes of the phyllosilicates and C asteroids. The CM chondrites can also be linked to the C asteroids by heating. We suggest that the CM chondrites are interior samples, and the presence of a 3 μm feature in C asteroid spectra also indicates the excavation of material.     

Material composition assessment and discovering sublimation activity on asteroids 145 Adeona, 704 Interamnia, 779 Nina,and 1474 Beira

Spectrophotometric observations of 145 Adeona, 704 Interamnia, 779 Nina, and 1474 Beira—asteroids of close primitive types—allowed us to detect similar mineralogical absorption bands in their reflectance spectra centered in the range 0.35 to 0.92 μm; the bands are at 0.38, 0.44, and 0.67–0.71 μm. On the same asteroids, the spectral signs of simultaneous sublimation activity were found for the first time. Namely, there are maxima at ～0.35–0.60 μm in the reflectance spectra of Adeona, Interamnia, and Nina and at ～0.55–075 μm in the spectra of Beira. We connect this activity with small heliocentric distances of the asteroids and, consequently, with a high insolation at their surfaces. Examination of the samples of probable analogues allowed us to identify Fe³⁺ and Fe²⁺ in the material of these asteroids through the mentioned absorption bands. For analogues, we took powdered samples of carbonaceous chondrites Orgueil (CI), Mighei (CM2), Murchison (CM2), and Boriskino (CM2), as well as hydrosilicates of the serpentine group. Laboratory spectral reflectance study of the samples of low-iron Mg serpentines (<2 wt % FeO) showed that the equivalent width of the absorption band centered at 0.44–0.46 μm strongly correlates with the content of Fe³⁺ in octahedral and tetrahedral coordinations. Our conclusion is that this absorption band can be used as a qualitative indicator of Fe³⁺ in the surface matter of asteroids and other solid celestial bodies. The comparison of the listed analog samples and the asteroids by parameters of the spectral features suggests that the silicate component of the asteroids' surface material is a mixture of hydrated and oxidized compounds, including oxides and hydroxides of bivalent and trivalent iron and carbonaceous-chondritic material. At the same time, the sublimation activity of Adeona, Interamnia, Nina, and Beira at high surface temperatures points to a substantial content of water ice in their material. This contradicts the previously existing notions on the C-type and similar asteroids as bodies containing water only in the bound state. Moreover, since the sublimation process simultaneously occurs in four primitive-type bodies at small heliocentric distances, we may suppose that this phenomenon is common for the main-belt asteroids.     

Spectral reflectance properties of carbonaceous chondrites: 2. CM chondrites

We have examined the spectral reflectance properties and available modal mineralogies of 39 CM carbonaceous chondrites to determine their range of spectral variability and to diagnose their spectral features. We have also reviewed the published literature on CM mineralogy and subclassification, surveyed the published spectral literature and added new measurements of CM chondrites and relevant end members and mineral mixtures, and measured 11 parameters and searched pair-wise for correlations between all quantities. CM spectra are characterized by overall slopes that can range from modestly blue-sloped to red-sloped, with brighter spectra being generally more red-sloped. Spectral slopes, as measured by the 2.4:0.56 μm and 2.4 μm:visible region peak reflectance ratios, range from 0.90 to 2.32, and 0.81 to 2.24, respectively, with values <1 indicating blue-sloped spectra. Matrix-enriched CM spectra can be even more blue-sloped than bulk samples, with ratios as low as 0.85. There is no apparent correlation between spectral slope and grain size for CM chondrite spectra - both fine-grained powders and chips can exhibit blue-sloped spectra. Maximum reflectance across the 0.3-2.5 μm interval ranges from 2.9% to 20.0%, and from 2.8% to 14.0% at 0.56 μm. Matrix-enriched CM spectra can be darker than bulk samples, with maximum reflectance as low as 2.1%. CM spectra exhibit nearly ubiquitous absorption bands near 0.7, 0.9, and 1.1 μm, with depths up to 12%, and, less commonly, absorption bands in other wavelength regions (e.g., 0.4-0.5, 0.65, 2.2 μm). The depths of the 0.7, 0.9, and 1.1 μm absorption features vary largely in tandem, suggesting a single cause, specifically serpentine-group phyllosilicates. The generally high Fe content, high phyllosilicate abundance relative to mafic silicates, and dual Fe valence state in CM phyllosilicates, all suggest that the phyllosilicates will exhibit strong absorption bands in the 0.7 μm region (due to Fe³⁺-Fe²⁺ charge transfers), and the 0.9-1.2 μm region (due to Fe²⁺ crystal field transitions), and generally dominate over mafic silicates. CM petrologic subtypes exhibit a positive correlation between degree of aqueous alteration and depth of the 0.7 μm absorption band. This is consistent with the decrease in fine-grained opaques that accompanies aqueous alteration. There is no consistent relationship between degree of aqueous alteration and evidence for a 0.65 μm region saponite-group phyllosilicate absorption band. Spectra of different subsamples of a single CM can show large variations in absolute reflectance and overall slope. This is probably due to petrologic variations that likely exist within a single CM chondrite, as duplicate spectra for a single subsample show much less spectral variability. When the full suite of available CM spectra is considered, few clear spectral-compositional trends emerge. This indicates that multiple compositional and physical factors affect absolute reflectance, absorption band depths, and absorption band wavelength positions. Asteroids with reflectance spectra that exhibit absorption features consistent with CM spectra (i.e., absorption bands near 0.7 and 0.9 μm) include members from multiple taxonomic groups. This suggests that on CM parent bodies, aqueous alteration resulted in the consistent production of serpentine-group phyllosilicates, however resulting absolute reflectances and spectral shapes seen in CM reflectance spectra are highly variable, accounting for the presence of phyllosilicate features in reflectance spectra of asteroids across diverse taxonomic groups.     

Spectral characteristics of iron-bearing phyllosilicates: Comparison to Orgueil (CI1), Murchison and Murray (CM2)

Abstract— Phyllosilicate alteration minerals are commonly found in low petrologic types of carbonaceous chondrites. Previous spectral studies have examined Mg-bearing phyllosilicates with limited success in matching the spectral properties of CM and CI chondrites. Transmission electron microscope and other analytical techniques suggest that Fe-bearing clays are more abundant in CI and CM chondrites than magnesian varieties. Here, we present the results of an examination of the reflectance spectra of Fe-phyllosilicates, including serpentines and berthierines, of which the latter were formerly known as septechlorites. We have measured the diffuse reflectance spectra of powdered samples from 0.3 to 25 μn. We find that these minerals provide a better spectral match to many of the features seen in CI and CM chondrites, and simple linear combinations of the spectra of both Fe- and Mg-phyllosilicates closely approximate the spectra of CM and CI chondrites.     

Infrared spectroscopy of interstellar nanodiamonds from the Orgueil meteorite

Abstract— We present results from an ongoing study of the infrared (IR) and optical properties of nanodiamonds, an objective of which is to identify spectral features in the laboratory that could also be used telescopically to trace the presence of these particles in the interstellar medium (ISM). Fourier transform mid-and far-infrared spectra of nanodiamond residue extracted from the Orgueil (CI) chondrite were acquired. All of the mid-IR bands initially present were found to diminish, with the exception of a band at ～1100 cm^?1, following additional oxidation of the diamonds. The ～1100 cm^?1 band can be predominantly attributed to adsorbed species, especially an ether-type linkage, while the “oxidisable” features seem to be associated with less stable, surface-bonded species and residual carbonaceous material. We obtained three far-IR features but are uncertain about the origin of those at 475 and 188 cm^?1. We did not obtain a feature at ～120 cm^?1 reported by another group but do not discount the possibility that the band at 188 cm^?1 could be related to it. The weak absorption band at 475 cm^?1 (21 μm) is especially interesting because it may be strong in emission from hot nanodiamonds and, therefore, related to the unidentified infrared feature (UIF) observed at this wavelength in the spectra of some C-rich protoplanetary nebulae.     

Detection and discrimination of sulfate minerals using reflectance spectroscopy

A suite of sulfate minerals were characterized spectrally, compositionally, and structurally in order to develop spectral reflectance-compositional-structural relations for this group of minerals. Sulfates exhibit diverse spectral properties, and absorption-band assignments have been developed for the 0.3-26 μm range. Sulfate absorption features can be related to the presence of transition elements, OH, H₂O, and SO₄ groups. The number, wavelength position, and intensity of these bands are a function of both composition and structure. Cation substitutions can affect the wavelength positions of all major absorption bands. Hydroxo-bridged Fe³⁺ results in absorption bands in the 0.43, 0.5, and 0.9 μm regions, while the presence of Fe²⁺ results in absorption features in the 0.9-1.2 μm interval. Fundamental SO bending and stretching vibration absorption bands occur in the 8-10, 13-18, and 19-24 μm regions (1000-1250, 550-770, and 420-530 cm⁻¹). The most intense combinations and overtones of these fundamentals are found in the 4-5 μm (2000-2500 cm⁻¹) region. Absorption features seen in the 1.7-1.85 μm interval are attributable to HOH/OH bending and translation/rotation combinations, while bands in the 2.1-2.7 μm regions can be attributed to H₂O- and OH-combinations as well as overtones of SO bending fundamentals. OH- and H₂O-bearing sulfate spectra are fundamentally different from each other at wavelengths below ∼6 μm. Changes in H₂O/OH content can shift SO band positions due to change in bond lengths and structural rearrangement. Differences in absorption band wavelength positions enable discrimination of all the sulfate minerals used in this study in a number of wavelength intervals. Of the major absorption band regions, the 4-5 μm region seems best for identifying and discriminating sulfates in the presence of other major rock-forming minerals.     

Thermal metamorphism of the C,G, B,and F asteroids seen from the 0.7 μm, 3 μm,and UV absorption strengths in comparison with carbonaceous chondrites

Abstract Thermal metamorphism study of the C, G, B, and F asteroids has been revisited using their UV, visible, NIR, and 3 μm reflectance spectra. High-quality reflectance spectra of seven selected C, G, B, and F asteroids have been compared with spectra for 29 carbonaceous chondrites, including thermally-metamorphosed CI/CM meteorites. There are three sets of spectral counterparts, among which 511 Davida and B-7904 are the most similar to each other in terms of both spectral shape and brightness. By comparing the 0.7 μm and 3 μm absorption strengths of 21 C, G, B, and F asteroids and heated Murchison samples, these asteroids have been grouped into three heating-temperature ranges. These correspond to (1) <400 °C: phyllosilicate-rich; (2) 400–600 °C: phyllosilicates transformed to anhydrous silicates; and (3) >600 °C: fully anhydrous. A good correlation between the UV and 3 μm absorption strengths has been confirmed for the C, G, B, and F asteroids and the CI, CM, and CR meteorites. A plot of the UV absorption strength vs. the IRAS diameter for 142 C, G, B, and F asteroids shows that the maximum UV absorption strength decreases as the diameter increases for the asteroids >60 km, with a notable exception, Ceres. These relationships suggest that some of the larger asteroids may be the heated inner portions of once larger bodies and that common CI/CM meteorites may have come from the lost outer portions, which escaped extensive late-stage heating events.     

Nature and degree of aqueous alteration in CM and CI carbonaceous chondrites

We investigated the petrologic, geochemical, and spectral parameters that relate to the type and degree of aqueous alteration in nine CM chondrites and one CI (Ivuna) carbonaceous chondrite. Our underlying hypothesis is that the position and shape of the 3 μm band is diagnostic of phyllosilicate mineralogy. We measured reflectance spectra of the chondrites under dry conditions (elevated temperatures) and vacuum (10^?8 to 10^?7 torr) to minimize adsorbed water and mimic the space environment, for subsequent comparison with reflectance spectra of asteroids. We have identified three spectral CM groups in addition to Ivuna. “Group 1,” the least altered group as determined from various alteration indices, is characterized by 3 μm band centers at longer wavelengths, and is consistent with cronstedtite (Fe‐serpentine). “Group 3,” the most altered group, is characterized by 3 μm band centers at shorter wavelengths and is consistent with antigorite (serpentine). “Group 2” is an intermediate group between group 1 and 3. Ivuna exhibits a unique spectrum that is distinct from the CM meteorites and is consistent with lizardite and chrysotile (serpentine). The petrologic and geochemical parameters, which were determined using electron microprobe analyses and microscopic observations, are found to be consistent with the three spectral groups. These results indicate that the distinct parent body aqueous alteration environments experienced by these carbonaceous chondrites can be distinguished using reflectance spectroscopy. High‐quality ground‐based telescopic observations of Main Belt asteroids can be expected to reveal not just whether an asteroid is hydrated, but also details of the alteration state.     

碳质球粒陨石有机物红外光谱研究

碳质球粒陨石是太阳系中最原始的物质之一.通过对碳质球粒陨石的光谱分析,可以建立其与母体小行星之间的联系,有助于探测小行星表面物质成分、研究太阳系早期的演化历史.研究了6个CM2型碳质球粒陨石和11个煤炭样品(碳质球粒陨石所含有机质的地球类比物)可见-远红外谱段反射光谱特征,并分析了它们与有机组分的关系.结果表明,对于不...     

Assessing the spatial variability of the ~3 μm OH/H2O absorption feature in CM2 carbonaceous chondrites

H₂O and OH are readily detected in hydrated minerals in CM chondrites via reflectance spectroscopy due to their characteristic vibration absorptions at infrared wavelengths. Previous spectroscopic work on bulk powdered CM chondrites has shown that spectral parameters, like the wavelength position of the “3 μm absorption feature,” vary systematically with the extent to which the samples have been aqueously altered. However, it is yet unclear how these spectral features may vary across an intact meteorite chip when measured at spatial scales smaller than that of the individual components of the meteorite. Here, we explore the spatial variability of this spectral feature and others on intact CM2 chips which, unlike powders, retain their petrologic and textural characteristics. We also model the modal mineralogy of the bulk meteorite powders and correlate this with key spectral features, demonstrating that microscope Fourier transform infrared spectroscopic mapping provides a powerful, rapid, and non-destructive technique for assessing compositional diversity and variations in water–rock interactions in chondritic planetary materials. In all CM2 chondrites studied here, we find that variations in the position, shape, and strength of the 3 μm absorption feature reveal a single chondrite can exhibit as much spectral variation as the entire suite of CM2 chondrites. The observed variations in the position and shape of the 3 μm feature within individual CM2 chondrite chips suggest a range of alteration products (e.g., Mg-rich to Fe-rich phyllosilicates) are present and record sub-mm scale variations in the amount and/or chemistry of the altering fluids. The samples having experienced the most progressive aqueous alteration show the least amount of variability in features like the 3 μm absorption band minimum position, whereas the least altered samples exhibit the most variability. We also find that the bulk spectral signatures in the least altered samples appear to be biased toward the spectral signatures of clasts versus matrix. By extension, asteroid reflectance spectra exhibiting 3 μm absorption features consistent with those measured here may be interpreted in a similar framework in which the spectrum of what may appear to be the least altered asteroids represents an average that belies the true diversity of mineralogy and chemistry of the body.     

Ceres’ spectral link to carbonaceous chondrites—Analysis of the dark background materials

Ceres’ surface has commonly been linked with carbonaceous chondrites (CCs) by ground‐based telescopic observations, because of its low albedo, flat to red‐sloped spectra in the visible and near‐infrared (VIS/NIR) wavelength region, and the absence of distinct absorption bands, though no currently known meteorites provide complete spectral matches to Ceres. Spatially resolved data of the Dawn Framing Camera (FC) reveal a generally dark surface covered with bright spots exhibiting reflectance values several times higher than Ceres’ background. In this work, we investigated FC data from High Altitude Mapping Orbit (HAMO) and Ceres eXtended Juling (CXJ) orbit (~140 m/pixel) for global spectral variations. We found that the cerean surface mainly differs by spectral slope over the whole FC wavelength region (0.4–1.0 μm). Areas exhibiting slopes ?1 constitute only ~3% of the cerean surface and mainly occur in the bright material in and around young craters, whereas slopes ≥?10% μm^?1 occur on more than 90% of the cerean surface; the latter being denoted as Ceres’ background material in this work. FC and Visible and Infrared Spectrometer (VIR) spectra of this background material were compared to the suite of CCs spectrally investigated so far regarding their VIS/NIR region and 2.7 μm absorption, as well as their reflectance at 0.653 μm. This resulted in a good match to heated CI Ivuna (heated to 200–300 °C) and a better match for CM1 meteorites, especially Moapa Valley. This possibly indicates that the alteration of CM2 to CM1 took place on Ceres.     

Spectral reflectance properties of carbonaceous chondrites: 3. CR chondrites

Powdered samples of a suite of 14 CR and CR-like chondrites, ranging from petrologic grade 1 to 3, were spectrally characterized over the 0.3–2.5 μm interval as part of a larger study of carbonaceous chondrite reflectance spectra. Spectral analysis was complicated by absorption bands due to Fe oxyhydroxides near 0.9 μm, resulting from terrestrial weathering. This absorption feature masks expected absorption bands due to constituent silicates in this region. In spite of this interference, most of the CR spectra exhibit absorption bands attributable to silicates, in particular an absorption feature due to Fe²⁺-bearing phyllosilicates near 1.1 μm. Mafic silicate absorption bands are weak to nonexistent due to a number of factors, including low Fe content, low degree of silicate crystallinity in some cases, and presence of fine-grained, finely dispersed opaques. With increasing aqueous alteration, phyllosilicate: mafic silicate ratios increase, resulting in more resolvable phyllosilicate absorption bands in the 1.1 μm region. In the most phyllosilicate-rich CR chondrite, GRO 95577 (CR1), an additional possible phyllosilicate absorption band is seen at 2.38 μm. In contrast to CM spectra, CR spectra generally do not exhibit an absorption band in the 0.65–0.7 μm region, which is attributable to Fe³⁺–Fe²⁺ charge transfers, suggesting that CR phyllosilicates are not as Fe³⁺-rich as CM phyllosilicates. CR2 and CR3 spectra are uniformly red-sloped, likely due to the presence of abundant Fe–Ni metal. Absolute reflectance seems to decrease with increasing degree of aqueous alteration, perhaps due to the formation of fine-grained opaques from pre-existing metal. Overall, CR spectra are characterized by widely varying reflectance (4–21% maximum reflectance), weak silicate absorption bands in the 0.9–1.3 μm region, overall red slopes, and the lack of an Fe³⁺–Fe²⁺ charge transfer absorption band in the 0.65–0.7 μm region.     

Bulk mineralogical changes of hydrous micrometeorites during heating in the upper atmosphere at temperatures below 1000 °C

Abstract— Small particles 200 μm in diameter from the hydrous carbonaceous chondrites Orgueil CI, Murchison CM2, and Tagish Lake were experimentally heated for short durations at subsolidus temperatures under controlled ambient pressures in order to examine the bulk mineralogical changes of hydrous micrometeorites during atmospheric entry. The three primitive meteorites consist mainly of various phyllosilicates and carbonates that are subject to decomposition at low temperatures, and thus the brief heating up to 1000 °C drastically changed the mineralogy. Changes included shrinkage of interlayer spacing of saponite due to loss of molecular water at 400–600 °C, serpentine and saponite decomposition to amorphous phases at 600 and 700 °C, respectively, decomposition of Mg‐Fe carbonate at 600 °C, recrystallization of secondary olivine and Fe oxide or metal at 700–800 °C, and recrystallization of secondary low‐Ca pyroxene at 800 °C. The ambient atmospheric pressures controlled species of secondary Fe phase: taenite at pressures lower than 10^?2 torr, magnesiowüstite from 10^?3 to 10^?1 torr, and magnetite from 10^?2 to 1 torr. The abundance of secondary low‐Ca pyroxene increases in the order of Murchison, Orgueil, and Tagish Lake, and the order corresponds to saponite abundance in samples prior to heating. Mineralogy of the three unmelted micrometeorites F96CI024, kw740052, and kw740054 were investigated in detail in order to estimate heating conditions. The results showed that they might have come from different parental objects, carbonaterich Tagish Lake type, carbonate‐poor Tagish Lake or CI type, and CM type, respectively, and experienced different peak temperatures, 600, 700, and 800?900 °C, respectively, at 60–80 km altitude upon atmospheric entry.     

Rapid contamination during storage of carbonaceous chondrites prepared for micro FTIR measurements

Abstract— Organic contamination (?2965 and ?1260 cm^?1peaks) was found on Tagish Lake (C2) and Murchison (CM2) carbonaceous chondrites containing abundant hydrous minerals by Fourier transform infrared (FTIR) microspectroscopy on the samples pressed on Al plates. On the other hand, anhydrous chondrite (Moss, CO3) was not contaminated. This contamination occurred within one day of storage, when the samples pressed on Al were stored within containers including silicone rubber mats. Volatile molecules having similar peaks to the contaminants were detected by long‐path gas cell FTIR measurements for the silicone rubber mat. Rapid adsorption of the volatile contaminants also occurred when silica gel and hydrous minerals such as serpentine were stored in containers including silicone rubber, silicone grease, or adhesive tape. However, they did not show any contamination when stored in glass and polystyrene containers without these compounds. Therefore, precious astronomical samples such as meteorites, interplanetary dust particles (IDPs), and mission‐returned samples from comets, asteroids, and Mars, should be measured by micro FTIR within one day of storage in glass containers without silicone rubber, silicone grease, or adhesive tape.     

Carbonates in CM chondrites: Complex formational histories and comparison to carbonates in CI chondrites

Abstract– CM chondrites are primitive solar‐system materials that have undergone high degrees of aqueous alteration, resulting in the formation of secondary minerals including carbonates. Two different carbonate minerals (calcite/aragonite and dolomite) together constitute 1.4–2.8 vol% of CM chondrites. In contrast, CI chondrites contain four different carbonate minerals: calcite/aragonite, dolomite, breunnerite, and siderite. CI chondrites have abundant dolomite, a mineral that seems to be absent in the most aqueously altered CM chondrites. In this study, carbonates in seven CM chondrites (Y‐791198, LaPaz Icefield 04796, Cold Bokkeveld, Nogoya, Queen Alexandra Range 93005, Allan Hills 83100, and Meteorite Hills 01070) were studied petrographically and by electron microprobe. The results indicate that carbonate formation in CM chondrites differs from that in CI chondrites and is more complex than previously recognized. Our studies of CM chondrites indicate that (1) carbonates formed on the parent asteroid in an aqueous environment that gradually changed in composition, (2) at some stage, Ca and Mg activities in the environment were high enough to form metastable dolomite, and (3) dolomites disappeared in the most aqueously altered CM chondrites.     

Infrared diffuse reflectances (2.5–25 μm) of some meteorites

We measured emissionless infrared diffuse reflectances of some meteorites by using a Fourier transform infrared spectrophotometer to obtain additional information on identification of asteroidal surface materials. Although the spectral features of diffuse reflectances are apparently different from those of transmission spectra, the absorption bands of constituent minerals can be detected. C2 carbonaceous chondrite materials can be distinguished from C3 materials by the depth of their hydration bands around 3 and 6 μm. These hydration bands do not lose contrast by pulverization of the sample. Acid dissolution experiment shows that the 6.8-μm band in the spectra of the Murchison (C2) meteorite is probably due to carbonates. The enstatite meteorite examined (Norton County) shows absorption bands around 10 μm caused by pyroxene unlike the iron meteorite examined (Mundrabilla). Because these latter two meteorite types give similar spectra without strong absorption bands in the UV-Visible-near IR region, middle infrared spectra should be helpful in interpreting asteroidal surface materials when combined with the UV-Visible-near IR spectra.