Carbonaceous micrometeorites from Antarctica

Abstract— Over 100 000 large interplanetary dust particles in the 50–500 μm size range have been recovered in clean conditions from ～600 tons of Antarctic melt ice water as both unmelted and partially melted/dehydrated micrometeorites and cosmic spherules. Flux measurements in both the Greenland and Antarctica ice sheets indicate that the micrometeorites deliver to the Earth's surface ～2000× more extraterrestrial material than brought by meteorites. Mineralogical and chemical studies of Antarctic micrometeorites indicate that they are only related to the relatively rare CM and CR carbonaceous chondrite groups, being mostly chondritic carbonaceous objects composed of highly unequilibrated assemblages of anhydrous and hydrous minerals. However, there are also marked differences between these two families of solar system objects, including higher C/O ratios and a very marked depletion of chondrules in micrometeorite matter; hence, they are “chondrites-without-chondrules.” Thus, the parent meteoroids of micrometeorites represent a dominant and new population of solar system objects, probably formed in the outer solar system and delivered to the inner solar system by the most appropriate vehicles, comets. One of the major purposes of this paper is to discuss applications of micrometeorite studies that have been previously presented to exobiologists but deal with the synthesis of prebiotic molecules on the early Earth, and more recently, with the early history of the solar system.     

Micrometeorites from the northern ice cap of the Novaya Zemlya archipelago,Russia: The first occurrence

Abstract— Glacial deposits at the margins of the ice cap of the northern island of the Novaya Zemlya archipelago, Russia, contain numerous spherules and rare scoriaceous particles thought to be extraterrestrial. The 1 Kyr old glacier has decreased in volume and coverage during the last 40 years, leaving the spherules contained in the ice at the margins of the glacier where they can be easily collected. The spherules are similar in their appearance, texture, and mineralogy to cosmic spherules found in deep‐sea sediments in Greenland and Antarctica. Silicate spherules have typical bar‐like textures (75%) or porphyritic textures (15%), while other spherules are glassy (7%). The spherules from Novaya Zemlya are altered only slightly. There are spherules consisting of iron oxides, metal cores with iron oxide rims, a continuous network of iron oxide dendrites in a glass matrix, and particles rich in chromite (3%). Some spherules contain metal droplets and relict forsterite and low‐Ca pyroxene. Silicate spherule compositions match compositions of other cosmic spherules. Both Nova Zemlya and other cosmic spherules are close to carbonaceous chondrite matrices in patterns of variations for Ca, Mg, Si, and Al, which might suggest that their predecessor was similar to carbonaceous chondrite matrices. Unmelted micrometeorites are generally depleted in Ca and Mg and enriched in Al relative to cosmic spherules. The depletion of the micrometeorites in Ca and Mg can be connected with their terrestrial alteration (Kurat et al. 1994), while the Al enrichment seems to be primary.     

Perceptive of the pyroxene-bearing micrometeorites and their relation to chondrites

We studied 149 pyroxenes from 69 pyroxene-bearing micrometeorites collected from deep-sea sediments of the Indian Ocean and South Pole Water Well at Antarctica, Amundsen-Scott South Pole station. The minor elements in pyroxenes from micrometeorites are present in the ranges as follows: MnO ~0.0–0.4 wt%, Al₂O₃ ~0.0–1.5 wt%, CaO ~0.0–1.0 wt%, Cr₂O₃ ~0.3–0.9 wt%, and FeO ~0.5–4 wt%. Their chemical compositions suggest that pyroxene-bearing micrometeorites are mostly related to precursors from carbonaceous chondrites rather than ordinary chondrites. The Fe/(Fe+Mg) ratio of the pyroxenes and olivines in micrometeorites shows similarities to carbonaceous chondrites with values lying between 0 and 0.2, and those with values beyond this range are dominated by ordinary chondrites. Atmospheric entry of the pyroxene-bearing micrometeorites is expected to have a relatively low entry velocity of <16 km s⁻¹ and high zenith angle (70–90°) to preserve their chemical compositions. In addition, similarities in the pyroxene and olivine mineralogical compositions between carbonaceous chondrites and cometary particles suggest that dust in the solar system is populated by materials from different sources that are chemically similar to each other. Our results on pyroxene chemical compositions reveal significant differences with those from ordinary chondrites. The narrow range in olivine and pyroxene chemical compositions are similar to those from carbonaceous chondrites, and a small proportion to ordinary chondrites indicates that dust is largely sourced from carbonaceous chondrite-type bodies.     

Unmelted cosmic metal particles in the Indian Ocean

Fe‐Ni metal is a common constituent of most meteorites and is an indicator of the thermal history of the respective meteorites, it is a diagnostic tool to distinguish between groups/subgroups of meteorites. In spite of over a million micrometeorites collected from various domains, reports of pure metallic particles among micrometeorites have been extremely rare. We report here the finding of a variety of cosmic metal particles such as kamacite, plessite, taenite, and Fe‐Ni beads from deep‐sea sediments of the Indian Ocean, a majority of which have entered the Earth unaffected by frictional heating during atmospheric entry. Such particles are known as components of meteorites but have never been found as individual entities. Their compositions suggest precursors from a variety of meteorite groups, thus providing an insight into the metal fluxes on the Earth. Some particles have undergone heating and oxidation to different levels during entry developing features similar to I‐type cosmic spherules, suggesting atmospheric processing of individual kamacites/taenite grains as another hitherto unknown source for the I‐type spherules. The particles have undergone postdepositional aqueous alteration transforming finally into the serpentine mineral cronstedtite. Aqueous alteration products of kamacite reflect the local microenvironment, therefore they have the potential to provide information on the composition of water in the solar nebula, on the parent bodies or on surfaces of planetary bodies. Our observations suggest it would take sustained burial in water for tens of thousands of years under cold conditions for kamacites to alter to cronstedtite.     

The solar system abundances of phosphorus and titanium and the nebular volatility of phosphorus

Abstract— The bulk chemical composition of Orgueil and 25 other carbonaceous chondrites was determined by x‐ray fluorescence analysis. The sample sizes of the analyzed meteorites were in all cases 120 mg. The abundances of P and Ti in Orgueil and Ivuna were precisely determined by the standard addition method. The new P CI abundance is 926 ± 65 ppm. Excluding the low P of Ivuna and one Orgueil sample with unusual chemistry gives a CI P content of 930 ± 23 ppm. A CI abundance of 926 ppm corresponds to a P/Si wt ratio of 8.66 times 10^?3 (atomic ratio 7.85 times 10^?3). For Ti a CI content of 458 ± 18 ppm and a Ti/Si wtratio of 4.28 times 10^?3 (atomic ratio 2.51 times 10^?3) were found. A Si content of 10.69% was obtained for average CI. The new P CI abundance is 20 to 30% below earlier estimates, while the Ti CI abundance is in agreement with earlier determinations. From the results of the analyses of bulk carbonaceous chondrites it is concluded: (1) Refractory element/Mg ratios increase from CI through CM and C3O to C3V, but ratios among Al, Ca and Ti are constant, except for low Ca/Al ratios in the reduced subgroup of C3V. (2) The Si/Mg ratios are constant in all groups of carbonaceous chondrites. (3) There is a volatility related depletion of Cr and Fe, but the Cr/Fe ratios are constant. (4) The sequence of volatility related depletions of the moderately volatile elements P, Au, As, Mn, and Zn follows condensation temperatures (except for As), if in condensation calculations non‐ideal solid solution in the host phase is considered.     

Oxygen isotopic and chemical composition of chromites in micrometeorites: Evidence of ordinary chondrite precursors

We identified 66 chromite grains from 42 of ~5000 micrometeorites collected from Indian Ocean deep‐sea sediments and the South Pole water well. To determine the chromite grains precursors and their contribution to the micrometeorite flux, we combined quantitative electron microprobe analyses and oxygen isotopic analyses by high‐resolution secondary ion mass spectrometry. Micrometeorite chromite grains show variable O isotopic compositions with δ¹⁸O values ranging from ?0.8 to 6.0‰, δ¹⁷O values from 0.3 to 3.6‰, and Δ¹⁷O values from ?0.9 to 1.6‰, most of them being similar to those of chromites from ordinary chondrites. The oxygen isotopic compositions of olivine, considered as a proxy of chromite in chromite‐bearing micrometeorites where chromite is too small to be measured in ion microprobe have Δ¹⁷O values suggesting a principal relationship to ordinary chondrites with some having carbonaceous chondrite precursors. Furthermore, the chemical compositions of chromites in micrometeorites are close to those reported for ordinary chondrite chromites, but some contribution from carbonaceous chondrites cannot be ruled out. Consequently, carbonaceous chondrites cannot be a major contributor of chromite‐bearing micrometeorites. Based on their oxygen isotopic and elemental compositions, we thus conclude with no ambiguity that chromite‐bearing micrometeorites are largely related to fragments of ordinary chondrites with a small fraction from carbonaceous chondrites, unlike other micrometeorites deriving largely from carbonaceous chondrites.     

Refractory inclusions from the ungrouped carbonaceous chondrites MacAlpine Hills 87300 and 88107

Abstract— MacAlpine Hills (MAC) 87300 and 88107 are two unusual carbonaceous chondrites that are intermediate in chemical composition between the CO3 and CM2 meteorite groups. Calcium‐aluminum‐rich inclusions (CAIs) from these two meteorites are mostly spinel‐pyroxene and melilite‐rich (Type A) varieties. Spinel‐pyroxene inclusions have either a banded or nodular texture, with aluminous diopside rimming Fe‐poor spinel. Melilite‐rich inclusions (Åk_4–42) are irregular in shape and contain minor spinel (FeO <1 wt%), perovskite and, more rarely, hibonite. The CAIs in MAC 88107 and 87300 are similar in primary mineralogy to CAIs from low petrologic grade CO3 meteorites but differ in that they commonly contain phyllosilicates. The two meteorites also differ somewhat from each other: melilite is more abundant and slightly more Al‐rich in inclusions from MAC 88107 than in those from MAC 87300, and phyllosilicate is more abundant and Mg‐poor in MAC 87300 CAIs relative to that in MAC 88107. These differences suggest that the two meteorites are not paired. The CAI sizes and the abundance of melilite‐rich CAIs in MAC 88107 and 87300 suggests a genetic relationship to CO3 meteorites, but the CAIs in both have suffered a greater degree of aqueous alteration than is observed in CO meteorites. Aluminum‐rich melilite in CAIs from both meteorites generally contains excess ²⁶Mg, presumably from the in situ decay of ²⁶Al. Although well‐defined isochrons are not observed, the ²⁶Mg excesses are consistent with initial ²⁶Al/²⁷Al ratios of approximately 3–5 times 10^?5. An unusual hibonite‐bearing inclusion is isotopically heterogeneous, with two large and abutting hibonite crystals showing significant differences in their degrees of mass‐dependent fractionation of ²⁵Mg/²⁴Mg. The two crystals also show differences in their inferred initial ²⁶Al/²⁷Al ratios, 1 × 10^?5 vs. ≤3 × 10^?6.     

A new variant of saponite‐rich micrometeorites recovered from recent Antarctic snowfall

Abstract– Eight saponite‐rich micrometeorites with very similar mineralogy were found from the recent surface snow in Antarctica. They might have come to Earth as a larger meteoroid and broke up into pieces on Earth, because they were recovered from the same layer and the same location of the snow. Synchrotron X‐ray diffraction (XRD) analysis indicates that saponite, Mg‐Fe carbonate, and pyrrhotite are major phases and serpentine, magnetite, and pentlandite are minor phases. Anhydrous silicates are entirely absent from all micrometeorites, suggesting that their parental object has undergone heavy aqueous alteration. Saponite/serpentine ratios are higher than in the Orgueil CI chondrite and are similar to the Tagish Lake carbonaceous chondrite. Transmission electron microscope (TEM) observation indicates that serpentine occupies core regions of fine‐grained saponite, pyrrhotite has a low‐Ni concentration, and Mg‐Fe carbonate shows unique concentric ring structures and has a mean molar Mg/(Mg + Fe) ratio of 0.7. Comparison of the mineralogy to hydrated chondrites and interplanetary dust particles (IDPs) suggests that the micrometeorites are most similar to the carbonate‐poor lithology of the Tagish Lake carbonaceous chondrite and some hydrous IDPs, but they show a carbonate mineralogy dissimilar to any primitive chondritic materials. Therefore, they are a new variant of saponite‐rich micrometeorite extracted from a primitive hydrous asteroid and recently accreted to Antarctica.     

Raman characterization of carbonaceous matter in CONCORDIA Antarctic micrometeorites

Abstract– We report a multi‐wavelength Raman spectroscopy study of carbonaceous matter in 38 Antarctic micrometeorites (AMMs) from the 2006 CONCORDIA collection. The particles were selected as a function of their degree of thermal alteration developed during the deceleration in the atmosphere. These samples range from unmelted (fine‐grained—Fg; ultracarbonaceous—UCAMMs) to partially melted AMMs (scorias—Sc) and completely melted particles (cosmic spherules—CS). More than half of the analyzed AMMs contain a substantial amount of polyaromatic carbonaceous matter with a high degree of disorder. The proportion of particles where carbon is not detected increase from the Fg to the Fg‐Sc and to the Sc‐AMMs, and no carbon is detected in CS. In addition, the spectral characteristics of the G and D bands of the carbonaceous matter in Sc‐AMMs plot apart from the trend formed by the data from Fg‐AMMs and UCAMMs. These results suggest that oxidation processes occurred during the deceleration of the particles in the atmosphere. In Fg‐AMMs and UCAMMs, the spectral characteristics of the G and D bands reveal the high degree of disorder of the carbonaceous matter, precluding a long duration thermal metamorphism on the parent body and suggesting that AMMs have a connection with C1–C2 chondrites. The Raman parameters of the deuterium‐rich carbonaceous matter of UCAMMs do not differ from that of Fg‐AMMs. Using a 244 nm excitation, we detected the cyanide (–CN) functional group for the first time in a UCAMM, reinforcing the likely cometary origin of this type of micrometeorites.     

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.     

Density,porosity, mineralogy,and internal structure of cosmic dust and alteration of its properties during high‐velocity atmospheric entry

X‐ray microtomography (XMT), X‐ray diffraction (XRD), and magnetic hysteresis measurements were used to determine micrometeorite internal structure, mineralogy, crystallography, and physical properties at μm resolution. The study samples include unmelted, partially melted (scoriaceous), and completely melted (cosmic spherules) micrometeorites. This variety not only allows comparison of the mineralogy and porosity of these three micrometeorite types but also reveals changes in meteoroid properties during atmospheric entry at various velocities. At low entry velocities, meteoroids do not melt and their physical properties do not change. The porosity of unmelted micrometeorites varies considerably (0–12%) with one friable example having porosity around 50%. At higher velocities, the range of meteoroid porosity narrows, but average porosity increases (to 16–27%) due to volatile evaporation and partial melting (scoriaceous phase). Metal distribution seems to be mostly unaffected at this stage. At even higher entry velocities, complete melting follows the scoriaceous phase. Complete melting is accompanied by metal oxidation and redistribution, loss of porosity (1 ± 1%), and narrowing of the bulk (3.2 ± 0.5 g cm^?3) and grain (3.3 ± 0.5 g cm^?3) density range. Melted cosmic spherules with a barred olivine structure show an oriented crystallographic structure, whereas other subtypes do not.     

Chondrules in Antarctic micrometeorites

Abstract— Previous studies of unmelted micrometeorites (>50 μm) recovered from Antarctic ice have concluded that chondrules, which are a major component of chondritic meteorites, are extremely rare among micrometeorites. We report the discovery of eight micrometeorites containing chondritic igneous objects, which strongly suggests that at least a portion of coarse‐grained crystalline micrometeorites represent chondrule fragments. Six of the particles are identified as composite micrometeorites that contain chondritic igneous objects and fine‐grained matrix. These particles suggest that at least some coarse‐grained micrometeorites (cgMMs) may be derived from the same parent bodies as fine‐grained micrometeorites. The new evidence indicates that, contrary to previous suggestions, the parent bodies of micrometeorites broadly resemble the parent asteroids of chondrulebearing carbonaceous chondrites.     

Manganese‐chromium formation intervals for chondrules from the Bishunpur and Chainpur meteorites

Abstract— Whole‐chondrule Mn‐Cr isochrons are presented for chondrules separated from the Chainpur (LL3.4) and Bishunpur (LL3.1) meteorites. The chondrules were initially surveyed by instrumental neutron activation analysis. LL‐chondrite‐normalized Mn/Cr, Mn/Fe, and Sc/Fe served to identify chondrules with unusually high or low Mn/Cr ratios, and to correlate the abundances of other elements to Sc, the most refractory element measured. A subset of chondrules from each chondrite was chosen for analysis by a scanning electron microscope equipped with an energy dispersive x‐ray spectrometer prior to high‐precision Cr‐isotopic analyses. ⁵³Cr/⁵²Cr correlates with ⁵⁵Mn/⁵²Cr to give initial (⁵³Mn/⁵⁵Mn)_I = (9.4 ± 1.7) × 10^?6 for Chainpur chondrules and (⁵³Mn/⁵⁵Mn)_I = (9.5 ± 3.1) × 10^?6 for Bishunpur chondrules. The corresponding chondrule formation intervals are, respectively, Δ_tLEW = ?10 ± 1 Ma for Chainpur and ?10 ± 2 Ma for Bishunpur relative to the time of igneous crystallization of the Lewis Cliff (LEW) 86010 angrite. Because Mn/Sc correlates positively with Mn/Cr for both the Chainpur and Bishunpur chondrules, indicating dependence of the Mn/Cr ratio on the relative volatility of the elements, we identify the event dated by the isochrons as volatility‐driven elemental fractionation for chondrule precursors in the solar nebula. Thus, our data suggest that the precursors to LL chondrules condensed from the nebula 5.8 ± 2.7 Ma after the time when initial (⁵³Mn/⁵⁵Mn)_I = (2.8 ± 0.3) × 10^?5 for calcium‐aluminum‐rich inclusions (CAIs), our preferred value, determined from data for (a) mineral separates of type B Allende CAI BR1, (b) spinels from Efremovka CAI E38, and (c) bulk chondrites. Mn‐Cr formation intervals for meteorites are presented relative to average I(Mn) = (⁵³Mn/⁵⁵Mn)_Ch = 9.46 × 10^?6 for chondrules. Mn/Cr ratios for radiogenic growth of ⁵³Cr in the solar nebula and later reservoirs are calculated relative to average (I(Mn), ?(⁵³Cr)_I) = ((9.46 ± 0.08) × 10^?6, ?0.23 ± 0.08) for chondrules. Inferred values of Mn/Cr lie within expected ranges. Thus, it appears that evolution of the Cr‐isotopic composition can be traced from condensation of CAIs via condensation of the ferromagnesian precursors of chondrules to basalt generation on differentiated asteroids. Measured values of ?(⁵³Cr) for individual chondrules exhibit the entire range of values that has been observed as initial ?(⁵³Cr) values for samples from various planetary objects, and which has been attributed to radial heterogeneity in initial ⁵³Mn/⁵⁵Mn in the early solar system. Estimated ⁵⁵Mn/⁵²Cr = 0.42 ± 0.05 for the bulk Earth, combined with ?(⁵³Cr) = 0 for the Earth, plots very close to the chondrule isochrons, so that the Earth appears to have the Mn‐Cr systematics of a refractory chondrule. Thus, the Earth apparently formed from material that had been depleted in Mn relative to Cr contemporaneously with condensation of chondrule precursors. If, as seems likely, the Earth's core formed after complete decay of ⁵³Mn, there must have been little differential partitioning of Mn and Cr at that time.     

Investigations on a Large Collection of Cosmic Dust From the Central Indian Ocean

We collected 1,245 spherules from the Central Indian Ocean basin by Magnetic cosmic dust collection (MACDUC) experiment raking the deep sea floor. This collection ranks among the large deep sea collections of cosmic dust. For this study, 168 particles are analyzed with SEM-EDS to characterise their cosmic nature and identify the processes that their morphological features, textures and chemical compositions reveal. All the three basic types of cosmic spherules have been identified: I-type, S-type and the G-type. The silicate or the S-type spherules are dominant in this collection. In all, 115 spherules were sectioned, polished and analyzed for major elements. I-type spherules are mainly composed of Fe and Ni oxides, some have metallic cores where appreciable amounts of Co is observed in addition to glassy phases with lithophile elements are also observed in these spherules. These evidences are supportive of the view that the I-type spherules could be metal grains from carbonaceous/unequilibrated chondritic bodies. The S-type spherules show elemental composition of Mg, Al, Si, Ca, Fe, and Ni approximately similar to chondritic compositions. In addition, some other rare particles such as an S-type sphere which contains a large zoned relict chromite crystal, other spheres with a semi-porphyritic/barred olivine texture are also observed. While most the S-type spherules appear to have carbonaceous chondrites as their parent bodies, the relict grain bearing spherule shows distinctly an ordinary chondritic parent body.     

Basaltic micrometeorites from the Novaya Zemlya glacier

Abstract– A large number of micrometeorites (MMs) was recovered from glacier deposits located at the north‐eastern passive margin of the Novaya Zemlya glacier sheet. Melted, scoriaceous, and unmelted micrometeorites (UMMs) are present. Unmelted micrometeorites are dominated mostly by chondritic matter, but also a few achondritic MMs are present. Here we report the discovery of four UMMs that, according to their texture, mineralogy, and chemistry, are identified as basaltic breccias. Mineral chemistry and Fe/Mn ratios of two basaltic micrometeorites indicate a possible relationship with eucrites and/or mesosiderites, whereas two others seem to have parents, which appear not to be present in our meteorite collections. The basaltic breccia UMMs constitute 0.5% of the total population of the Novaya Zemlya MM suite. This content should be lowered to 0.25% because the Novaya Zemlya MM collection appears to be biased with carbonaceous UMMs being underrepresented.     

Brownish inclusions and dark streaks in Libyan Desert Glass: Evidence for high‐temperature melting of the target rock

Abstract– Dark streaks and different types of inclusions in Libyan Desert Glass (LDG) collected from the LDG strewn field in Egypt were investigated. Rare transparent spherules enclosed in the glassy matrix are characterized by concentric cracks, irregular internal cracks, intense twinning, and considerable amounts of Ti and Al. Raman spectra show that the spherules are α‐cristobalite. Their occurrence together with lechatelierite indicates quick heating of the source rock to at least 1550 °C, followed by rapid quenching leading to crystallization of β‐cristobalite, which upon cooling inverted into α‐cristobalite. Brownish inclusions are irregularly shaped, elongated objects with smooth contacts to the surrounding glass. They contain small roundish to elliptical droplets, and a few larger angular grains, which compositionally and according to their Raman spectra most closely resemble low‐Ca, Al‐rich orthopyroxene. Composition and texture of the orthopyroxene suggest that the brownish inclusions formed by incomplete melting of an Al‐rich orthopyroxene bearing precursor, e.g., mafic phases present in desert surface sands or also of orthopyroxene‐bearing granulite dykes in the LDG target. Experimental data on Ca‐poor enstatite also support that the inclusions were heated to about 1550 °C. Analyses of dark streaks in LDG reveal high abundances of Al, Ti, Mn, Cr, Fe, and Ni and a pronounced correlation between the abundances of Cr, Mn, Fe, and Ni. As the Fe/Ni, Mn/Ni, and Cr/Ni ratios are all clearly nonchondritic, the source of this material is most likely terrestrial and the dark streaks studied here represent a different type of schlieren compared to those which contain a meteoritic component. These findings suggest LDG formation during a short high‐temperature event. Melting of Al‐rich orthopyroxene bearing target material seems to suggest an asteroid impact rather than a near‐surface airburst.     

Numbers,types, and compositions of an unbiased collection of cosmic spherules

Abstract— Micrometeorites collected from the bottom of the South Pole water well (SPWW) may represent a complete, well‐preserved sample of the cosmic dust that accreted on Earth from 1100–1500 A.D. We classified 1588 cosmic spherules in the size range 50–800 μm. The collection has 41% barred olivine spherules, 17% glass spheres, 12% cryptocrystalline spherules, 11% porphyritic olivine spherules, 12% relicgrain‐bearing spherules, 3% scoriaceous spherules, 2% I‐type spherules, 1% Ca‐AI‐Ti‐rich (CAT) spherules, and 1% G‐type spherules. We also found bubbly glass spherules, spherules with glass caps, and ones with sulfide coatings—particles that are absent from other collections. A classification sequence of the stony spherules (scoriaceous, relic‐grain‐bearing, porphyritic, barred olivine, cryptocrystalline, glass, and CAT) is consistent with progressive heating and evaporation of Fe from chondritic materials. The modern‐day accretion rate and size distribution measured at the SPWW can account for the stony spherules present in deep‐sea collection through preferential dissolution of glass and small stony spherules. However, weathering alone cannot account for the high accretion rate of I‐type spherules determined for two deep‐sea collections. The SPWW collection provides data to constrain models of atmospheric‐entry heating and to assess the effects of terrestrial weathering.     

Differentiation processes in FeO‐rich asteroids revealed by the achondrite Lewis Cliff 88763

Olivine‐dominated (70–80 modal %) achondrite meteorite Lewis Cliff (LEW) 88763 originated from metamorphism and limited partial melting of a FeO‐rich parent body. The meteorite experienced some alteration on Earth, evident from subchondritic Re/Os, and redistribution of rhenium within the sample. LEW 88763 is texturally similar to winonaites, has a Δ¹⁷O value of ?1.19 ± 0.10‰, and low bulk‐rock Mg/(Mg+Fe) (0.39), similar to the FeO‐rich cumulate achondrite Northwest Africa (NWA) 6693. The similar bulk‐rock major‐, minor‐, and trace‐element abundances of LEW 88763, relative to some carbonaceous chondrites, including ratios of Pd/Os, Pt/Os, Ir/Os, and ¹⁸⁷Os/¹⁸⁸Os (0.1262), implies a FeO‐ and volatile‐rich precursor composition. Lack of fractionation of the rare earth elements, but a factor of approximately two lower highly siderophile element abundances in LEW 88763, compared with chondrites, implies limited loss of Fe‐Ni‐S melts during metamorphism and anatexis. These results support the generation of high Fe/Mg, sulfide, and/or metal‐rich partial melts from FeO‐rich parent bodies during partial melting. In detail, however, LEW 88763 cannot be a parent composition to any other meteorite sample, due to highly limited silicate melt loss (0 to <<5%). As such, LEW 88763 represents the least‐modified FeO‐rich achondrite source composition recognized to date and is distinct from all other meteorites. LEW 88763 should be reclassified as an anomalous achondrite that experienced limited Fe,Ni‐FeS melt loss. Lewis Cliff 88763, combined with a growing collection of FeO‐rich meteorites, such as brachinites, brachinite‐like achondrites, the Graves Nunataks (GRA) 06128/9 meteorites, NWA 6693, and Tafassasset, has important implications for understanding the initiation of planetary differentiation. Specifically, regardless of precursor compositions, partial melting and differentiation processes appear to be similar on asteroidal bodies spanning a range of initial oxidation states and volatile contents.     

Nickel abundance in stony cosmic spherules: Constraining precursor material and formation mechanisms

Abstract– We report bulk and olivine compositions in 66 stony cosmic spherules (Na₂O < 0.76 wt%), 200–800 μm in size, from the Transantarctic Mountains, Antarctica. In porphyritic cosmic spherules, relict olivines that survived atmospheric entry heating are always Ni‐poor and similar in composition to the olivines in carbonaceous or unequilibrated ordinary chondrites (18 spherules), and equilibrated ordinary chondrites (one spherule). This is consistent with selective survival of high temperature, Mg‐rich olivines during atmospheric entry. Olivines that crystallized from the melts produced during atmospheric entry have NiO contents that increase with increasing NiO in the bulk spherule, and that range from values similar to those observed in chondritic olivines (NiO generally <0.5 wt%) to values characteristic of olivines in meteoritic ablation spheres (NiO > 2 wt%). Thus, NiO content in olivine cannot be used alone to distinguish meteoritic ablation spheres from cosmic spherules, and the volatile element contents have to be considered. We propose that the variation in NiO contents in cosmic spherules and their olivines is the result of variable content of Fe, Ni metal in the precursor. NiO contents in olivines and in cosmic spherules can thus be used to discuss their parent body. Ni‐poor spherules can be derived from C‐rich and/or metal‐poor precursors, either related to CM, CI, CR chondrites or to chondritic fragments dominated by silicates, regardless of the parent body. Ni‐rich spherules (NiO > 0.7 wt%) that represent 55% of the 47 barred‐olivine spherules we studied, were derived from the melting of C‐poor, metal‐rich precursors, compatible with ordinary chondrite or CO, CV, CK carbonaceous chondrite parentages.     

Chondritic models of 4 Vesta: Implications for geochemical and geophysical properties

Simple mass‐balance and thermodynamic constraints are used to illustrate the potential geochemical and geophysical diversity of a fully differentiated Vesta‐sized parent body with a eucrite crust (e.g., core size and density, crustal thickness). The results of this analysis are then combined with data from the howardite–eucrite–diogenite (HED) meteorites and the Dawn mission to constrain Vesta's bulk composition. Twelve chondritic compositions are considered, comprising seven carbonaceous, three ordinary, and two enstatite chondrite groups. Our analysis excludes CI and LL compositions as plausible Vesta analogs, as these are predicted to have a negative metal fraction. Second, the MELTS thermodynamic calculator is used to show that the enstatite chondrites, the CV, CK and L‐groups cannot produce Juvinas‐like liquids, and that even for the other groups, depletion in sodium is necessary to produce liquids of appropriate silica content. This conclusion is consistent with the documented volatile‐poor nature of eucrites. Furthermore, carbonaceous chondrites are predicted to have a mantle too rich in olivine to produce typical howardites and to have Fe/Mn ratios generally well in excess of those of the HEDs. On the other hand, an Na‐depleted H‐chondrite bulk composition is capable of producing Juvinas‐like liquids, has a mantle rich enough in pyroxene to produce abundant howardite/diogenite, and has a Fe/Mn ratio compatible with eucrites. In addition, its predicted bulk‐silicate density is within 100 kg m^?3 of solutions constrained by data of the Dawn mission. However, oxidation state and oxygen isotopes are not perfectly reproduced and it is deduced that bulk Vesta may contain approximately 25% of a CM‐like component. Values for the bulk‐silicate composition of Vesta and a preliminary phase diagram are proposed.