Meteorite Groups Research Articles

Petrogenesis of lunar granulitic breccia meteorites Northwest Africa 15062 and 15063

AbstractWe present petrology and mineralogy for two lunar granulitic breccia meteorites that were detected in Northwest Africa (NWA), the samples NWA 15062 and NWA 15063. The fragments primarily consist of plagioclase and olivine mineral clasts, with minor amounts of anorthosite clasts and one troctolite clast. The anorthosite clasts are dominated by plagioclase/maskelynite, with minor olivine and pyroxene. A troctolite clast, composed of olivine and maskelynite, occurs in NWA 15063. The olivine clasts display mosaic extinction and usually have a homogeneous Mg‐rich composition. However, all olivine mineral clasts exhibit two distinct ranges of their major element composition (Mg#: 85–88 and 77–78, respectively). Large individual plagioclase clasts show heterogeneous compositions (Ab content: 2.5–4.8) and have different Raman peak positions in different domains. The matrix of the meteorites appears semitransparent and is composed of olivine and pyroxene aggregates associated with maskelynite, constituting a granoblastic texture. Pyroxenes of the matrix are dominantly enstatites, associated with a few augites. Both meteorite samples exhibit shock‐induced melt veins ranging from 50 to 200 μm width. These melt veins traverse the entire samples and contain rare, very fine‐grained (2–3 μm) Mg‐rich olivine clasts (Mg# = 90–93) and mafic silicate glass. Some Cr‐spinel grains exhibit slight compositional zonation, characterized by a magnesium‐rich core (Mg# = 56, Cr# = 23) and Cr‐rich rims (Mg# = 50, Cr# = 28), with decomposition at the edges. The significantly differing Mg# contents of the mafic silicate minerals in the matrix, lithic clasts, and mineral clasts of the two meteorites indicate a diverse origin of the clasts. Based on their petrology, mineral chemistry, and bulk composition, NWA 15062 and NWA 15063 are classified as anorthositic troctolitic granulitic polymict breccia. Textural evidence suggests that the parent rocks of NWA 15062 and NWA 15063 were affected by high pressure of up to 30 GPa during impact‐induced shock metamorphism, causing crystal structure deformation in olivine and the transformation of plagioclase to maskelynite. During cooling from peak temperatures of 1600–1700°C, the coarse‐grained maskelynite mineral clasts were partially devitrified, and the granoblastic texture of the matrix was developed. Mg‐rich anorthosite was formed before this shock event. Cr‐spinel was formed in a troctolitic melt, which was probably differentiated after the crystallization of anorthite and magnesium‐rich olivine. However, the possibility of the formation of the Mg‐rich melt through interaction with the lunar anorthositic crust cannot be ruled out. The meteorite NWA 15062/15063 strongly resembles the textural, chemical, and mineralogical characteristics of the NWA 5744 meteorite group. Therefore, we interpret the two samples as a new member of the NWA 5744 meteorite group.

Triple-oxygen isotopes of stony micrometeorites by secondary ion mass spectrometry (SIMS): Olivine, basaltic glass and iron oxide matrix effects for sensitive high-mass resolution ion microprobe-stable isotope (SHRIMP-SI).

Micrometeorites are extraterrestrial particles smaller than ~2mm in diameter, most of which melted during atmospheric entry and crystallised or quenched to form 'cosmic spherules'. Their parentage among meteorite groups can be inferred from triple-oxygen isotope compositions, for example, by secondary ion mass spectrometry (SIMS). This method uses sample efficiently, preserving spherules for other investigations. While SIMS precisions are improving steadily, application requires assumptions about instrumental mass fractionation, which is controlled by sample chemistry and mineralogy (matrix effects). We have developed a generic SIMS method using sensitive high-mass resolution ion micro probe-stable isotope (SHRIMP-SI) that can be applied to finely crystalline igneous textures as in cosmic spherules. We correct for oxygen isotope matrix effects using the bulk chemistry of samples obtained by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and model bulk chemical compositions as three-component mixtures of olivine, basaltic glass and Fe-oxide (magnetite), finding a unique matrix correction for each target. Our first results for cosmic spherules from East Antarctica compare favourably with established micrometeorite groups defined by precise and accurate but consumptive bulk oxygen isotope methods. The Fe-oxide content of each spherule is the main control on magnitude of oxygen isotope ratio bias, with effects on δ18O up to ~6‰. Our main peak in compositions closely coincides with so-called 'Group 1' objects identified by consumptive methods. The magnitude of SIMS matrix effects we find is similar to the previous intraspherule variations, which are now the limiting factor in understanding their compositions. The matrix effect for each spherule should be assessed quantitatively and individually, especially addressing Fe-oxide content. We expect micrometeorite triple-oxygen isotope compositions obtained by SIMS to converge on the main clusters (Groups 1 to 4) after correction firstly for magnetite content and secondarily for other phases (e.g., basaltic glass) in each target.

Radial transport and nebular thermal processing of millimeter‐sized solids in the Solar protoplanetary disk inferred from Cr‐Ti‐O isotope systematics of chondrules

AbstractUnderstanding the material transport and mixing processes in the Solar protoplanetary disk provides important constraints on the origin of chemical and isotopic diversities of our planets. The limited extent of radial transport and mixing between the inner and outer Solar System has been suggested based on a fundamental isotopic dichotomy between non‐carbonaceous (NC) and carbonaceous (CC) meteorite groups. The limited transport and mixing could be further tested by tracing the formation regions of individual meteoritic components, such as Ca‐Al‐rich inclusions (CAIs) and chondrules. Here, we show further evidence for the outward transport of CAIs and chondrules from the inner and subsequent thermal processing in the outer region of the protoplanetary disk based on the petrography and combined Cr‐Ti‐O isotope systematics of chondrules from the Vigarano‐like (CV) carbonaceous chondrite Allende. One chondrule studied consists of an olivine core that exhibits NC‐like Ti and O, but CC‐like Cr isotopic signatures, which is enclosed by a pyroxene igneous rim with CC‐like O isotope ratios. These observations indicate that the olivine core formed in the inner Solar System. The olivine core then migrated into the outer Solar System and experienced nebular thermal processing that generated the pyroxene igneous rim. The nebular thermal processing would result in Cr isotope exchange between the olivine core and CC‐like materials, but secondary alteration effects on the parent body are also responsible for the CC‐like Cr isotope signature. By combining previously reported Cr‐Ti‐O isotope systematics of CV chondrules, we show that some CV chondrules larger than ~1 mm would have formed in the inner Solar System. The accretion of the millimeter‐sized, inner Solar System solids onto the CV carbonaceous chondrite parent body would require their very early migration into the outer Solar System within the first 1 million years after the Solar System formation.

Spectral properties of ablating meteorite samples for improved meteoroid composition diagnostics

Emission spectra and diagnostic spectral features of a diverse range of ablated meteorite samples with a known composition are presented. We aim to provide a reference spectral dataset to improve our abilities to classify meteoroid composition types from meteor spectra observations. The data were obtained by ablating meteorite samples in high-enthalpy plasma wind tunnel facilities recreating conditions characteristic of low-speed meteors. Near-UV to visible-range (320–800 nm) emission spectra of 22 diverse meteorites captured by a high-resolution Echelle spectrometer were analyzed to identify the characteristic spectral features of individual meteorite groups. The same dataset captured by a lower-resolution meteor spectrograph was applied to compare the meteorite data with meteor spectra observations. Spectral modeling revealed that the emitting meteorite plasma was characterized by temperatures of 3700–4800 K, similar to the main temperature component of meteors. The studied line intensity variations were found to trace the differences in the original meteorite composition and thus can be used to constrain the individual meteorite classes. We demonstrate that meteorite composition types, including ordinary chondrites, carbonaceous chondrites, various achondrites, stony-iron and iron meteorites, can be spectrally distinguished by measuring relative line intensities of Mg I, Fe I, Na I, Cr I, Mn I, Si I, H I, CN, Ni I, and Li I. Additionally, we confirm the effect of the incomplete evaporation of refractory elements Al, Ti, and Ca, and the presence of minor species Co I, Cu I, and V I.

Quantification of evaporative loss of volatile metals from planetary cores and metal-rich planetesimals

The processes responsible for the isotopic compositions and abundances of volatile elements in the early solar system remain highly debated. Orders of magnitude variation of (highly) volatile elements exist between different magmatic iron meteorite groups, but it is unclear to what extent their depletions can be explained by evaporation from metal melts during parent body accretion and/or subsequent break up. To this end, we present 86 new evaporation experiments with the aim of constraining the volatility of most volatile metals from metallic melts. The results confirm the previously proposed important effects of S in metal melt on the volatility of the elements of interest governed by their S-loving or S-phobic behavior. Nominally S-loving elements In, Sn, Te, Pb and Bi are significantly more volatile in Fe melt relative to FeS liquid, whereas nominally S-avoiding elements Ga and Sb are more volatile in FeS liquid relative to Fe melt, at a given pressure and temperature. The newly derived volatility sequences for S-free/poor and S-rich metallic melts were also compared with commonly used volatility models based on condensation temperatures. The results indicate significant differences between the latter, including the much more volatile behavior of Te, relative to Se, in both explored bulk compositions, which are traditionally assumed to be equally volatile. The (minimum) degree of volatile element depletion due to evaporation was quantified using the new experimental results and models. A comparison between the volatile element depletions in magmatic iron meteorites and the predicted depletions appropriate for evaporation from Fe melts shows that the latter depletions can be easily reconciled with (an) evaporation event(s). Altogether, the new data and models will provide an important framework when more accurate and precise estimates of magmatic iron meteorite bulk volatile element contents are available.

The source craters of the martian meteorites: Implications for the igneous evolution of Mars.

Approximately 200 meteorites come from ~10 impact events on the surface of Mars, yet their pre-ejection locations are largely unknown. Here, we combine the results of diverse sets of observations and modeling to constrain the source craters for several groups of martian meteorites. We compute that ejection-paired groups of meteorites are derived from lava flows within the top 26 m of the surface. We link ejection-paired groups to specific source craters and geologic units, providing context for these important samples, reconciling microscopic observations with remote sensing records, and demonstrating the potential to constrain the ages of their source geologic units. Furthermore, we show that there are craters that may have produced martian meteorites not represented in the world's meteorite collections that have yet to be discovered.

Chondrule sizes within the CM carbonaceous chondrites and measurement methodologies

AbstractThe sizes of chondrules are a valuable tool for understanding relationships between meteorite groups and the affinity of ungrouped chondrites, documenting temporal/spatial variability in the solar nebula, and exploring the effects of parent body processing. Many of the recently reported sizes of chondrules within the CM carbonaceous chondrites differ significantly from the established literature average and are more closely comparable to those of chondrules within CO chondrites. Here, we report an updated analysis of chondrule dimensions within the CM group based on data from 1937 chondrules, obtained across a suite of CM lithologies ranging from petrologic subtypes CM2.2 to CM2.7. Our revised average CM chondrule size is 194 μm. Among the samples examined, a relationship was observed between petrologic subtype and chondrule size such that chondrule long‐axis lengths are greater in the more highly aqueously altered lithologies. These findings suggest a greater similarity between the CM and CO chondrites than previously thought and support arguments for a genetic link between the two groups (i.e., the CM‐CO clan). Using the 2‐D and 3‐D data gathered, we also apply numerous stereological corrections to examine their usefulness in correcting 2‐D chondrule measurements within the CM chondrites. Alongside this analysis, we present the details of a standardized methodology for 2‐D chondrule size measurement to facilitate more reliable inter‐study comparisons.

Impactor identification with spallogenic Cr isotopes: The Wabar impact craters (Saudi Arabia)

AbstractPrecise measurements of Cr isotopic composition of terrestrial impactites have successfully provided evidence for the presence of extraterrestrial material and have, in some cases, allowed the identification of the type of impactor responsible for the formation of the impact structure. The high Cr abundance in most meteorite groups aids in detecting extraterrestrial contamination while their distinct isotopic compositions can help with the identification of the nature of the projectile. However, this common approach of detection and identification of extraterrestrial contamination using mass‐independent 53Cr and 54Cr variations fails when the impactor type is an iron meteorite because of their low Cr abundances (which are in a similar range to terrestrial rocks). The present study demonstrates the viability of a spallogenic Cr contribution in iron meteorites (resulting from their long cosmic ray exposure times), which compensates for their low Cr abundances and facilitates the identification of iron‐meteoritic contamination in terrestrial impactites. Thus, it broadens the scope of impactors (and impactites) that can be investigated using mass‐independent Cr isotopes from solely chondrites and primitive achondrites to include iron meteorites. The Wabar impact craters are an optimal candidate for this study, characterized by low weathering, diverse impactites, partial meteorite survival, substantial impactor material contamination, and a felsic target lithology with low background Cr concentration. The Cr isotopic composition of the Wabar background sand, which represents the target lithology, is indistinguishable from the terrestrial Cr isotopic composition range, whereas the Wabar iron meteorites show coupled spallogenic excesses in ε53Cr and ε54Cr. The Cr isotopic compositions of Wabar impactites show resolved deviations from the terrestrial Cr isotopic composition, thereby indicating the presence of Wabar meteoritic contamination. Moreover, the study demonstrates that even an impactor with a non‐carbonaceous chondritic origin, such as a IIIAB iron meteorite, can have a carbonaceous chondrite‐like signature in ε54Cr anomalies due to spallogenic Cr contamination. The study advocates for a comprehensive investigation combining platinum group elements and Cr (and/or Ni, Ru) isotopes to accurately characterize impactor types.

Recurrent planetesimal formation in an outer part of the early solar system

The formation of planets in our solar system encompassed various stages of accretion of planetesimals that formed in the protoplanetary disk within the first few million years at different distances to the sun. Their chemical diversity is reflected by compositionally variable meteorite groups from different parent bodies. There is general consensus that their formation location is roughly constrained by a dichotomy of nucleosynthetic isotope anomalies, relating carbonaceous (C) meteorite parent bodies to the outer protoplanetary disk and the non-carbonaceous (NC) parent bodies to an origin closer to the sun. It is a common idea, that in these inner parts of the protoplanetary disks, planetesimal accretion processes were faster. Testing such scenarios requires constraining formation ages of meteorite parent bodies. Although isotopic age dating can yield precise formation ages of individual mineral constituents of meteorites, such ages frequently represent mineral cooling ages that can postdate planetesimal formation by millions or tens of millions of years, depending on the cooling history of individual planetesimals at different depths. Nevertheless, such cooling ages provide a detailed thermal history which can be fitted by thermal evolution models that constrain the formation age of individual parent bodies. Here we apply state-of-the-art thermal evolution models to constrain planetesimal formation times particular in the outer solar system formation region of C meteorites. We infer a temporally distributed accretion of various parent bodies from <0.6\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$<0.6$$\\end{document} Ma to ≈4\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\approx 4$$\\end{document} Ma after solar system formation, with 3.7 Ma and 2.5-2.75\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$2.5-2.75$$\\end{document} Ma for the parent bodies of CR1-3 chondrites and the Flensburg carbonaceous chondrite, and <0.6\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$<0.6$$\\end{document} and <0.7\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$<0.7$$\\end{document} Ma for the parent bodies of differentiated achondrites NWA 6704 and NWA 011, respectively. This implies that accretion processes in the C reservoir started as early as in the NC reservoir and were operating throughout typical protoplanetary disk lifetimes, thereby producing differentiated parent bodies with carbonaceous compositions in addition to undifferentiated C chondrite parent bodies. The accretion times correlate inversely with the degree of the meteorites’ alteration, metamorphism, or differentiation. The accretion times for the CM, CI, Ryugu, and Tafassite parent bodies of 3.8 Ma, 3.8 Ma, 1-3\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$1-3$$\\end{document} Ma, and 1.1 Ma, respectively, fit well into this correlation in agreement with the thermal and alteration conditions suggested by these meteorites. Our results indicate that individual planetesimals formed rapidly (i.e., within <1\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$<1$$\\end{document} Ma), however, distinct planetesimals formed recurrently throughout the total lifetime of the protoplanetary disk. Rapid individual formation is consistent with streaming instabilities assisted by gravitational collapse. However, obviously not the total dust inventory was consumed at early disk evolution stages, so there must have been some delay mechanisms, e.g. collisional destruction of precursor aggregates due to high impact velocities induced by radial drift phenomena. This counterbalance enabled late (>2-3\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$>2-3$$\\end{document} Ma) accretion of C planetesimals beyond the snow line which escaped severe planetesimal heating and volatile loss, hence, preserving their volatiles, especially water. Only this delayed formation of water-rich planetesimals allowed Earth to accrete sufficient water to become a habitable planet, preventing it from being a bone dry planet.

Pb Isotope Signature of a Low-μ (238U/204Pb) Lunar Mantle Component

Abstract The chemical and isotopic characteristics of terrestrial basalts are constrained within the concept of mantle chemical geodynamics that explains the existing variety of basaltic rocks within a framework of several end-member reservoirs in Earth’s mantle. In contrast, there is no comparable fully developed model explaining the isotopic composition of lunar basaltic rocks, in part owing to the lack of well-constrained age–isotope relationships in different groups of basalts identified on the Moon. Notably, the absence of agreement upon ages includes basalts from a unique group of meteorites collectively known as ‘YAMM’ (basalts Yamato-793169: Y-793169, Asuka-881757: A-881757, Miller Range 05035: MIL 05035 and regolith breccia Meteorite Hill 01210: MET 01210), which appear to show chemical signatures different from all other known lunar basaltic rocks. We present high-precision Pb–Pb ages and initial Pb isotopic ratios for two samples from this group, MIL 05035 and A-881757. These meteorites have Pb isotope ratios different from those of the other lunar basalts, suggesting they are derived from a distinct and depleted mantle source, with a 238U/204Pb ratio (μ value) lower than any other mantle source. Their depletion in rare earth elements, in conjunction with recalculated initial Nd and Sr isotopic ratios from published data and using our new age, appear to support this conclusion. The chemical and Sr-Nd-Pb isotopic characteristics of this low-μ source appear to be the opposite of those of the KREEP reservoir and many, if not all, features described in other lunar basalts (such as low- and high-Ti mare basalts) can be explained by a binary mixing of material derived from low-μ and KREEP-like reservoirs. This mixing might be the result of a slow, convection-like mantle overturn.

Unusual sources of fossil micrometeorites deduced from relict chromite in the small size fraction in ~467 Ma old limestone

ABSTRACTExtraterrestrial chrome spinel and chromite extracted from the sedimentary rock record are relicts from coarse micrometeorites and rarely meteorites. They are studied to reconstruct the paleoflux of meteorites to the Earth and the collisional history of the asteroid belt. Minor element concentrations of Ti and V, and oxygen isotopic compositions of these relict minerals were used to classify the meteorite type they stem from, and thus to determine the relative meteorite group abundances through time. While coarse sediment‐dispersed extraterrestrial chrome‐spinel (SEC) grains from ordinary chondrites dominate through the studied time windows in the Phanerozoic, there are exceptions: We have shown that ~467 Ma ago, 1 Ma before the breakup of the L chondrite parent body (LCPB), more than half of the largest (&gt;63 μm diameter) grains were achondritic and originated from differentiated asteroids in contrast to ordinary chondrites which dominated the meteorite flux throughout most of the past 500 Ma. Here, we present a new data set of oxygen isotopic compositions and elemental compositions of 136 grains of a smaller size fraction (32–63 μm) in ~467 Ma old pre‐LCPB limestone from the Lynna River section in western Russia, that was previously studied by elemental analysis. Our study constitutes the most comprehensive oxygen isotopic data set of sediment‐dispersed extraterrestrial chrome spinel to date. We also introduce a Raman spectroscopy‐based method to identify SEC grains and distinguish them from terrestrial chrome spinel with ~97% reliability. We calibrated the Raman method with the established approach using titanium and vanadium concentrations and oxygen isotopic compositions. We find that ordinary chondrites are approximately three times more abundant in the 32–63 μm fraction than achondrites. While abundances of achondrites compared to ordinary chondrites are lower in the 32–63 μm size fraction than in the &gt;63 μm one, achondrites are approximately three times more abundant in the 32–62 μm fraction than they are in the present flux. We find that the sources of SEC grains vary for different grain sizes, mainly as a result of parent body thermal metamorphism. We conclude that the meteorite flux composition ~467 Ma ago ~1 Ma before the breakup of the LCPB was fundamentally different from today and from other time windows studied in the Phanerozoic, but that in contrast to the large size fraction ordinary chondrites dominated the flux in the small size fraction. The high abundance of ordinary chondrites in the studied samples is consistent with the findings based on coarse extraterrestrial chrome‐spinel from other time windows.

Large Carbonaceous Chondrite Parent Bodies Favored by Abundance–Volatility Modeling: A Possible Chemical Signature of Pebble Accretion

Primitive meteorite groups such as the Vigarano, Mighei, and Karoonda carbonaceous chondrites have enigmatic patterns of elemental abundances, with moderately volatile elements—those that transition from vapor to condensate between ∼400 and ∼900 K—defining plateaus of subequal abundances despite a wide range in volatility. In detail, each group defines a plateau with distinctive nonmonotonic “chemical fingerprints” that have been attributed to combinations of mixing, vaporization/condensation, and fluid-mediated metasomatism—but the extent to which these processes can reproduce the observed variability has not been quantified. Starting with primitive Ivuna chondrite, a two-stage, two-component equilibrium condensation–vaporization model—with gravity implemented as Jeans escape—can explain large-scale plateaus in these chondrite groups, as well as more complex, nonmonotonic small-scale variations. For all three chondritic meteorite groups, models favor earlier high-temperature fractionation under low-gravity conditions followed by a low-temperature fractionation event that took place on a protoplanet at least as large as Ceres. The second fractionation event may represent the fractionation of incoming materials to the planetesimal during protracted pebble accretion. Models with only thermally driven volatile loss, gravity, and mixing can explain more than 80% of the observed compositional variability in these meteorite groups. In our five-parameter model, using only five randomly selected elements yields uselessly large ranges of planet sizes and temperatures, ranges that converge with increasing numbers of elements. These results suggest that even simple models are prone to generating inaccurate conclusions when constrained by too few observations, a fault likely held by more complex models as well.

Dense collection areas and terrestrial alteration of meteorites in the Atacama Desert

AbstractIn the last 15 years, more than 2700 meteorites have been recovered and officially classified from the Atacama Desert. Although the number of meteorites collected in the Atacama has risen, the physical and climatic properties of the dense collection areas (DCAs) have not been fully characterized. In this article, we compiled the published data of all classified meteorites found in the Atacama Desert to (i) describe the distribution by meteorite groups, (ii) compare the weathering degree of chondrites among different Atacama DCAs and other hot and cold deserts, and (iii) determine the preservation conditions of chondrites in the main Atacama DCAs in relation with the local climatic conditions. The 35 DCAs so far identified in the Atacama Desert are located in three main morphotectonic units: The Coastal Range (CR), Central Depression (CD), and Pre‐Andean Range/Basement. A comparison with reported weathering data from other cold and hot deserts indicates that the mean terrestrial weathering of Atacama chondrites (W1–2), displays less alteration than other hot deserts (W2–3) and resembles the weathering distribution of the Antarctic meteorites (W1–2). The highest abundance of Atacama chondrites with low weathering (≤W2) is localized in the CD (78.8%, N = 1435), which is protected from the coastal fog influence and seasonal rainfalls and displays the oldest surfaces in the Atacama Desert. The morphogenetic classification based on present‐day temperatures and precipitations of the main Atacama DCAs reveals similar regional/subregional climatic conditions in the most productive areas and a truly productive surface for meteorite recovery between 5% and 58% of the quadrangles formally defined for each Atacama DCA. Our morphogenetic classification lacks consideration of some meteorological parameters such as the coastal fog, so it cannot fully explain the differences in weathering patterns among CR chondrites. Future studies of chondrite preservation in the Atacama DCAs should consider other meteorological variables such as relative humidity, specific humidity, or dew point, in combination with exposure ages of meteorites and its surfaces.

Unusual specimens from Estonia

Samples of metal and glass found in 2019 in the vicinity of Tallinn are described. The structure, composition and properties of the samples were analyzed. According to their structural and chemical characteristics, the samples belong to the same parent body and differ from representatives of known groups of iron meteorites, artificial ferroalloys, technical and natural glasses. The glass matrix of the samples contains “folds” and “stripes”. Metallic inclusions in glass predominantly consist of alpha iron with an admixture of troilite. Carbon inclusions predominate in the metal matrix of the samples. Analogues of the material composition of the samples are protvanites. The possible cosmic origin of the samples is confirmed by surface regmaglypts, fullerenes, other carbon phases and cohenite.

Role of redox conditions and thermal metamorphism in the preservation of Cr isotopic anomalies in components of non-carbonaceous chondrites

Mass-independent isotopic anomalies in meteorites are probes to the dynamics and evolution of the protoplanetary disc and the reservoirs from which planetary bodies accreted. Variable Cr nucleosynthetic compositions between meteorite groups are observed but the cause is not well understood. Investigations on presolar carriers in unequilibrated chondrites are thus required to establish these relationships. For that purpose, we analysed the Cr isotope compositions of leachates (stepwise dissolution solutions) of one ordinary chondrite and two enstatite chondrites of EL and EH subgroups previously measured for Nd and Sm isotopes. The leachates of the ordinary chondrite display large variations of their Cr isotope compositions, whereas the leachates of the enstatite chondrites show very limited variations of their nucleosynthetic compositions, confirming other studies. The Cr isotope compositions of leachates of unequilibrated chondrites are significantly modified by thermal processing and aqueous alteration under various conditions. The leachates of the enstatite chondrites are relatively homogeneous for Cr isotope composition, suggesting that presolar carriers of Cr are not stable under very reduced conditions and are likely oxidised phases. After careful examination of the role of parent body processing, we conclude that there is one predominant presolar carrier enriched in 54Cr that produced most of the nucleosynthetic variations observed in leachates. This carrier is likely depleted in the carbonaceous reservoir relative to the non-carbonaceous reservoir. The drastically different isotope compositions of Cr and heavy refractory lithophile elements such as Nd of leachates of chondrites reflect relative preservation biases of their respective presolar carriers, namely a still poorly characterised presolar oxide and silicon carbide (SiC), respectively.

Mineralogical anatomy of the Cr-rich quenched angrite Northwest Africa 12774: Implication to mantle heterogeneity

Angrites are a small group of basaltic meteorites and their origin is currently disputed. Among these, Northwest Africa (NWA) 12774 is a quenched angrite that was reported having an anomalously high bulk Cr2O3 content (∼0.45 wt%). However, the reason behind this anomaly, which is critical for understanding the evolution of the angrite parent body, remains unknown. Here, we performed a detailed petrographic, mineralogical, and bulk oxygen and chromium isotopic composition study on this meteorite. NWA 12774 consists of porous olivine macrocrysts, phenocrysts of olivine and Al-Ti-rich augite, and spinel micro-phenocrysts with fine-grained groundmass. The olivine macrocrysts and the magnesian cores of olivine phenocrysts show compositional correlations distinctly different from typical olivine phenocrysts. The olivine macrocrysts contain small chromite/chrome-spinel inclusions which have the highest Cr2O3 content (53.2 wt%) for chromite/spinel in angrites to date. Based on these textural and chemical features, the olivine macrocrysts and the magnesian cores of olivine phenocrysts are identified as xenocrysts. Some pyroxene phenocrysts contain regions with complexly zoned microtextures, which have much larger chemical variations compared with those with simply zoned microtextures. The regions with complexly zoned microtextures are likely to be of xenocrystic origin. The bulk Cr2O3 content in NWA 12774 was estimated through two approaches, both of which show the bulk Cr2O3 content to be around 0.3 wt% or possibly up to ∼ 0.45 wt%, which is consistent with previously measured values. The high Cr2O3 content in NWA 12774 could be attributed to both the high abundance of spinel micro-phenocrysts and their high Cr2O3 contents, rather than the presence of Cr-rich xenocrysts. The calculated melt rare earth element concentration in NWA 12774 equilibrated with the most Mg-rich augite is essentially identical to those in LEW 87051 and Asuka 881371, which however have Cr2O3 contents much lower than NWA 12774. We suggest that the mantle source of NWA 12774 may not be as depleted in Cr and probably other volatile elements as other angrite sources. The various Cr2O3 contents in different quenched angrites probably reflect that their mantle sources have not been homogenized.

Chemical and genetic characterization of the ungrouped pallasite Lieksa

ABSTRACTThe meteorite Lieksa was found in 2017 in Löpönvaara, Finland, and later donated to the Finnish Museum of Natural History. Here, we report siderophile element concentrations, genetic isotopic data, and a metal–silicate segregation age for the meteorite. The ~280 g Lieksa is ~80% metal and ~20% silicate and oxide inclusions by volume, with the inclusions consisting primarily of Fe‐rich olivine. Due to Lieksa's silicate content, coupled with a texture characterized by metal enclosing the silicates, it has been classified as a pallasite. Lieksa's olivine and bulk chemical characteristics are distinct from those of the known pallasite and iron meteorite groups, consistent with its classification as ungrouped. The meteorite exhibits a flat, chondrite‐normalized highly siderophile element pattern, consistent with an origin as an early crystallization product from a metallic melt with chondritic relative abundances. Molybdenum, Ru, and 183W isotopic data indicate that Lieksa formed in the non‐carbonaceous (NC) domain of the solar nebula. Radiogenic 182W abundances for Lieksa yield a model metal–silicate segregation age of 1.5 ± 0.8 Myr after calcium‐aluminum‐rich inclusion formation, which is within the range established for other NC‐type pallasite and iron meteorite parent bodies.

CLASSIFICATION OF THE GEOCHEMICAL COMPOSITION OF METEORITE OF PUNGGUR (ASTOMULYO) BY k-NEAREST NEIGHBOR ALGORITHM

The fall of a meteorite in Astomulyo Village, Punggur, Lampung Province in early 2021 is an interesting topic for further study. This rare object has been suggested to have a unique geochemical composition and a special connection with other meteorites. We aimed to trace its classification by comparing it with other well-known meteorites studied previously. We approach the classification process using the k-nearest neighbor algorithm. The database used 211 represents the geochemical data for each known meteorite group from chemical analyses of meteorites. As a result, we identified that with a k-value = 5 and the proportion of test data 5/95 (in %), the geochemical composition of this meteorite is relatively close to that of the H-type chondrite group with a value accuracy of 91.67%. These results are consistent with the fact that the meteorite of Punggur has a high total iron and metallic composition.

The “Meteorite meter”: A handheld instrument for the combined measurement of magnetic susceptibility and electrical conductivity, with application to meteorite identification and classification

AbstractWe developed a simple, handheld, and user‐friendly magnetic susceptibility meter specialized for the identification of meteorites. The measurement is based on an LC resonance circuit. When provided with a rough estimate of the sample mass, the instrument displays directly the mass‐normalized magnetic susceptibility expressed in logχm (with χm in 10−9 m3 kg−1), a parameter that is widely used in the classification of meteorites. Moreover, the measurement of the impedance of the LC resonator provides a proxy of the electrical conductivity (C‐index) that can be helpful to distinguish metal‐bearing samples from magnetite‐bearing samples. This C‐index offers an additional diagnostic for the identification of meteorites. Our tests demonstrate that the precision and the accuracy of this instrument called “Meteorite meter” (MetMet) are sufficient to allow distinguishing most meteorites from most terrestrial rocks, for a minimum recommended sample mass of 5 g. The distinction of some meteorite groups is also possible, in particular the separation of the three ordinary chondrite groups. Meteorite hunters, collectors, and curators and non‐specialists, including children, can use this instrument as a guidance in the identification and classification of meteorites. This kind of instrument has an immense advantage over the widely used testing of meteorites with magnets, as it does not affect the paleomagnetic records of meteorites that are highly valuable for scientists.

Evaporation of moderately volatile elements from metal and sulfide melts: Implications for volatile element abundances in magmatic iron meteorites

Volatile element abundances in magmatic iron meteorites provide fundamental insights into the processing of volatile elements in the early solar system. Although Cu, Ge and Ag concentrations of magmatic iron meteorites deviate up to 4 orders of magnitude between different magmatic iron meteorite groups, the role of evaporation on these volatile abundances is poorly constrained. Here, we experimentally assess the volatility of Cu, Ge, Ag, S, Cr, Co, Ni, Mo, Ru, Pd, W, Re and Ir from metal and sulfide melts as a function of pressure (10−4 and 1 bar), temperature (1573–1823 K) and time (5–120 min) for two end-member compositions (Fe versus FeS). These novel experiments demonstrate that the presence of S is a major parameter in establishing the volatility of Cu, Ge, Mo, Ag, Ru, W, Re and Ir. At constant P-T and time, the volatility of Ge, Mo, Ru, W, Re and Ir is greatly increased in the presence of S, whereas Cu and Ag are less volatile in the presence of S. At 1773 K and ∼0.001 bar, the volatility of S is sufficiently high that the degassed FeS liquid showed immiscibility of a S-rich sulfide and a S-poor Fe melt. Empirical equations were derived that predict the evaporative loss of Cu, Ge, Mo, Ag from Fe and/or FeS liquid as a function of temperature and time. A comparison of the newly derived volatility sequences with commonly applied 50% condensation temperature models shows that the condensation temperature models cannot be applied to sulfur-bearing Fe liquids and therefore to magmatic iron meteorites. Application of the new models on previously derived elemental depletions in the IVB parent body shows that evaporation, if it occurred, cannot have taken place under S-rich conditions. The latter would result in a depletion of Mo, which is not observed for the IVB irons. However, evaporation of a S-free or S-poor Fe liquid reproduces the observed volatility depletion trend for IVB irons under a wider range of temperature and evaporation times, demonstrating the potential importance of evaporative loss on the IVB parent body.