Meteoritics & Planetary Science最新文献

Carbonates, as secondary minerals found in CM chondrites, have been widely employed for reconstructing the composition of the fluids from which they precipitated. They also offer valuable insights into the hydrothermal evolution of their parent bodies. In this study, we demonstrate that high-resolution cathodoluminescence (HR-CL) analyses of calcites derived from the brecciated Cold Bokkeveld CM2 chondrite can effectively reveal subtle compositional features and intricate zoning patterns. We have identified two distinct types of cathodoluminescence (CL) centers: a blue emission band (approximately 375–425 nm), associated with intrinsic structural defects, and a lower energy orange extrinsic emission (around 620 ± 10 nm), indicating the presence of Mn cations. These compositional variations enable discrimination between the calcite grain types previously designated as T1 and T2 in studies of CM chondrites. T1 calcites exhibit variable CL and peripheral Mn enrichments, consistently surrounded by a rim composed of Fe-S-rich serpentine–tochilinite assemblage. Conversely, T2 calcites display homogeneous CL and more abundant lattice defects. These polycrystalline aggregates of calcite grains, devoid of serpentine, contain Fe-Ni sulfide inclusions and directly interface with the matrix. We propose that changes in the Mn content of calcite (indicated by the intensity of orange CL emission) are influenced by variations in redox potential (Eh) and pH of the fluid phase. This proposed hydrothermal evolution establishes a parallel between terrestrial serpentinization followed by carbonation processes and the aqueous alteration of CM chondrites, warranting further exploration and investigation of this intriguing similarity.

Type II chondrules have higher oxidation states than type I chondrules; in ordinary chondrites (OC), type II chondrules tend to be larger, richer in bulk Fe, and have higher densities than type I chondrules. Magnesian type IA chondrules tend to be richer in ¹⁶O than type II chondrules. Because the aerodynamic behavior of a particle is a function of the product of its size and density, type I and type II chondrules (or their precursors) were partly separated in the ordinary chondrite zone of the solar nebula prior to the accretion of OC parent asteroids. LL chondrites acquired a chondrule population with the highest type II/type I ratios, L chondrites acquired chondrules with an intermediate ratio, and H chondrites acquired chondrules with the lowest type II/type I ratios. This contributed to the observed differences among OC groups in oxidation state and O-isotopic composition: in going from H to L to LL, mean oxidation state increases and mean Δ¹⁷O values increase. Higher oxidation is marked by increases in the FeO contents of olivine, low-Ca pyroxene, chromite, and ilmenite; increases in the TiO₂ content of chromite; and increases in the Co content of kamacite.

Enstatite meteorites, both aubrites and enstatite chondrites, formed under exceptionally reducing conditions, similar to the planet Mercury. Despite being reduced, the MESSENGER mission showed that the surface of Mercury is more enriched in volatiles (e.g., S, Na, K, Cl) than previously thought. To better understand the mineral hosts of these volatiles and how they formed, this work examines the chemistry and petrographic settings of a rare, K-bearing sulfide called djerfisherite within enstatite chondrites and aubrites. The petrographic settings of djerfisherite within aubrites suggest this critical host of Cl formed after both the crystallization of troilite and exsolution of daubréelite. Djerfisherite is commonly observed as a rim on other sulfides and in contact with metal. We present an alteration model for djerfisherite formation in aubrite meteorites, whereby troilite and Fe-Ni metal are altered through anhydrous, alkali- and Cl-rich fluid metasomatism on the aubrite parent body to produce secondary djerfisherite. Moreover, we observe a loss of volatiles in djerfisherite within impact melted regions of the Miller Range 07139 EH3 chondrite and the Bishopville aubrite and explore the potential for impact devolatilization changes to sulfide chemistry on other reduced bodies in the Solar System. Vapor or fluid phase interactions are likely important in the formation of volatile-rich phases in reduced systems. While most Na and K on the mercurian surface is expected to be hosted in feldspar, djerfisherite is likely a minor, but critical, reservoir for K, Na, and Cl. Djerfisherite present on reduced bodies, such as Mercury, may represent sulfides formed via late-stage, primary metasomatism.

A melilite-rich, compact type A Ca-Al-rich inclusion (CAI), KU-N-02, from the reduced CV3 chondrite Northwest Africa 7865, is mantled by an åkermanite-poor layer. We carried out a combined study of petrographic observations and in situ O and Al–Mg isotopic measurements for KU-N-02. The core shows a typical texture of igneous compact type A CAIs. The mantle consists of spinel, åkermanite-poor melilite, and perovskite. Individual mantle melilite crystals show reverse zoning toward the crystal grain boundary, in contrast to core melilite crystals showing normal zoning. The O isotopic compositions of the minerals in KU-N-02 plot along the carbonaceous chondrite anhydrous mineral line on a three O-isotope diagram. The mantle and core spinel crystals are uniformly ¹⁶O-rich (Δ¹⁷O ~ −23‰). The mantle melilite crystals exhibit variable O isotopic compositions ranging between Δ¹⁷O ~ −2‰ and −9‰, in contrast to the uniformly ¹⁶O-poor (Δ¹⁷O ~ −2‰) core melilite. The mantle melilite crystals also exhibit variable δ²⁵Mg values (δ²⁵Mg_DSM-3 ~ −2‰ to +3‰) compared with the nearly constant δ²⁵Mg values of the core melilite (δ²⁵Mg_DSM-3 ~ +2‰). The mantle minerals are likely to have formed by condensation from the solar nebular gas after core formation. The Al–Mg mineral isochrons of the core and mantle give initial ²⁶Al/²⁷Al ratios of (4.66 ± 0.15) × 10⁻⁵ and (4.74 ± 0.14) × 10⁻⁵, respectively. The age difference between the core and mantle formation is estimated to be within ~0.05 Myr, implying that both melting and condensation processes in the variable O isotopically solar nebular environments occurred within a short time during single CAI formation.

Elmshorn fell April 25, 2023, about 30 km northwest of the city of Hamburg (Germany). Shortly after the fall, 21 pieces were recovered totaling a mass of 4277 g. Elmshorn is a polymict and anomalous H3-6 chondritic, fragmental breccia. The rock is a mixture of typical H chondrite lithologies and clasts of intermediate H/L (or L, based on magnetic properties) chondrite origin. In some of the 21 pieces, the H chondrite lithologies dominate, while in others the H/L (or L) chondrite components are prevalent. The H/L chondrite assignment of these components is based on the mean composition of their olivines in equilibrated type 4 fragments (~Fa_21–22). The physical properties like density (3.34 g cm⁻³) and magnetic susceptibility (logχ <5.0, with χ in 10⁻⁹ m³ kg⁻¹) are typical for L chondrites, which is inconsistent with the oxygen isotope compositions: all eight O isotope analyses from two different fragments clearly fall into the H chondrite field. Thus, the fragments found in the strewn field vary in mineralogy, mineral chemistry, and physical properties but not in O isotope characteristics. The sample most intensively studied belongs to the stones dominated by H chondrite lithologies. The chemical composition and nucleosynthetic Cr and Ti isotope data are typical for ordinary chondrites. The noble gases in Elmshorn represent a mixture between cosmogenic, radiogenic, and primordially trapped noble gases, while a solar wind component can be excluded. Because the chondritic rock of Elmshorn contains (a) H chondrite parent body interior materials (of types 5 and 6), (b) chondrite parent body near-surface materials (of types 3 and 4), (c) fragments of an H/L chondrite (dominant in many stones), (d) shock-darkened fragments, and (e) clasts of various types of impact melts but no solar wind-implanted noble gases, the different components cannot have been part of a parent body regolith. The most straightforward explanation is that the fragmental breccia of Elmshorn represents a reaccreted rock after a catastrophic collision between an H chondrite parent body and another body with H/L (or L) chondrite characteristics but with deviating O isotope values (i.e. that of H chondrites), complete disruption of the bodies, mixing, and reassembly. This is the only straightforward way that the implantation of solar wind gases could have been avoided in this kind of complex breccia. The gas retention ages of about 2.8 Gyr possibly indicate the closure time after the catastrophic collision between H and H/L (or L) chondrite parent bodies, while the cosmic ray exposure age for Elmshorn, which had a preatmospheric radius of 25–40 cm, is ~17–20 Myr.

CM chondrites are samples from primitive water-rich asteroids that formed early in the solar system; many record evidence for silicate rock–liquid water interaction. Many CM chondrites also exhibit well-developed fine-grained rims (FGRs) that surround major components, including chondrules and refractory inclusions. Previous studies have shown that Aguas Zarcas, a CM2 chondrite fall recovered in 2019, is a breccia consisting of several lithologies. Here, we present a study of Aguas Zarcas using optical microscopy, scanning electron microscopy, and electron probe microanalysis, focusing on brecciation and aqueous alteration on the parent body. We observed two lithologies within our sample, separated by a distinct textural and chemical boundary. The first lithology has a higher chondrule abundance (“chondrule-rich”) and significantly larger FGRs compared to the second lithology (“chondrule-poor”), even for similarly sized chondrules. We observed clear compositional differences between the two lithologies and more multilayered FGRs in the chondrule-rich lithology. We determined that the chondrule-rich lithology is less altered (petrologic type 2.7–2.8) and displays larger FGRs to chondrule ratios compared to the more altered chondrule-poor lithology (petrologic type 2.5–2.6). These observations are contrary to previous models that predict aqueous alteration as a cause of FGR formation in the parent body. Our observed differences in Mg and Fe distribution in the lithology matrices alongside variable FGR thickness suggest distinct formation environments. We propose that the Aguas Zarcas parent body was subjected to several minor and major brecciation events that mixed different materials with variable degrees of aqueous alteration together, in agreement with previous studies.

We analyzed the methanol extracts of six pristine specimens of the Tagish Lake meteorite (TL1, TL4, TL5A, TL6, TL7, and TL10a) and heated and unheated samples of Allende using high-performance liquid chromatography coupled with high-resolution, accurate mass–mass spectrometry (HPLC-HRAM-MS). All samples contained ppm levels of sulfate and methyl sulfate. The most abundant organosulfur compound in the methanol extracts of the Tagish Lake and Allende samples was methyl sulfate, which was likely formed primarily via an esterification reaction between intrinsic sources of methanol and sulfate. A homologous series of polythionic acids was also observed in the extracts of the Tagish Lake specimens and Allende. The polythionic acids were the most abundant soluble inorganic sulfur species found in the meteorites. Our results were confirmed using retention time, accurate mass, isotope matching, and tandem mass spectrometry (MS/MS). Hydroxymethanesulfonic acid, previously reported in Tagish Lake, was found only in an unheated Allende sample and in low abundance. Here, we propose possible sulfate formation pathways that begin with interstellar dimethyl sulfide, dimethyl disulfide, methyl sulfide, or methanethiol via cold, nebular processes within the interstellar medium and continue via MSA as an intermediary compound ending within planetary bodies with sulfate and methyl sulfate as the final products.