Impact glasses in fallout suevites from the Ries impact structure,Germany: An analytical SEM study

Abstract— t‐Impact‐generated glasses from fallout suevite deposits at the Ries impact structure have been investigated using analytical scanning electron microscopy. Approximately 320 analyses of glass clasts were obtained. Four glass types are distinguished on the basis of composition and microtextures. Type 1 glasses correspond to the aerodynamically shaped glass bombs studied previously by many workers. Major oxide concentrations indicate the involvement of granitic rocks, amphibolites, and minor Al‐rich gneisses during melting. Type 2 glasses are chemically heterogeneous, even within individual clasts, with variations of several wt% in most of the major oxides (e.g., 57–70 wt% SiO₂). This suggests incomplete mixing of: 1) mineral‐derived melts or 2) whole rock melts from a wide range of lithologies. Aluminium‐rich clinopyroxene and Fe‐Mg‐rich plagioclase quench crystals are present in type 1 and 2 glasses, respectively. Type 3 glasses contain substantial amounts of H₂O (?12–17 wt%), low SiO₂ (50–53 wt%), high Al₂O₃ (17–21 wt%), and high CaO (5–7 wt%) contents. This suggests an origin due to shock melting of part of the sedimentary cover. Type 4 glasses form a ubiquitous component of the suevites. Based on their high SiO₂ content (?85–100 wt%), the only possible protolith are sandstones in the lowermost part of the sedimentary succession. Calcite forms globules within type 1 glasses, with which it develops microtextures indicative of liquid immiscibility. Unequivocal evidence also exists for liquid immiscibility between what are now montmorillonite globules and type 1, 2, and 4 glasses, indicating that montmorillonite was originally an impact melt glass. Clearly, the melt zone at the Ries must have incorporated a substantial fraction of the sedimentary cover, as well as the underlying crystalline basement rocks. Impact melts were derived from different target lithologies and these separate disaggregated melts did not substantially mix in most cases (type 2, 3, and 4 glasses and carbonate melts).     

Water in tektites and impact glasses by fourier-transformed infrared spectrometry

Abstract— To improve the scarce data base of H₂O content in tektites and impact glasses, we analyzed 26 tektites from all four strewn fields and 25 impact glass samples for their H₂O content. We used the fourier-transformed infrared (FTIR) spectrometry method, which permits measurement of areas of ～40 μm in diameter. Our results show that the tektites have H₂O contents ranging from 0.002 to 0.030 wt% (average 0.014 ± 0.008 wt%). Ivory Coast tektites have the lowest H₂O abundances (0.002–0.003 wt%), and Muong Nong-type indochinites and some North American tektites having the highest contents (up to ～0.03 wt%). Impact glass samples (from the Zhamanshin, Aouelloul, and Rio Cuarto craters) yielded H₂O contents of 0.008 to 0.13 wt% H₂O. Typical impact glasses from the Aouelloul and Zhamanshin craters have low H₂O contents (0.008 to 0.063 wt%). Libyan Desert Glasses and Rio Cuarto glasses have higher H₂O contents (～0.11 wt%). We also analyzed glasses of unknown origin (e.g., urengoites; glass fragments from Tikal), which showed very low H₂O contents, in agreement with an origin by impact. Our data confirm that all tektites found on land have very low H₂O contents (<0.03 wt% H₂O), while impact glasses have slightly higher H₂O contents. Both glass types are very dry compared to volcanic glasses. This study confirms that the low H₂O contents (<0.05 wt%) of such glasses can be considered good evidence for an origin by impact.     

Composition of impact melt particles and the effects of post‐impact alteration in suevitic rocks at the Yaxcopoil‐1 drill core,Chicxulub crater,Mexico

Abstract Petrographical and chemical analysis of melt particles and alteration minerals of the about 100 m‐thick suevitic sequence at the Chicxulub Yax‐1 drill core was performed. The aim of this study is to determine the composition of the impact melt, the variation between different types of melt particles, and the effects of post‐impact hydrothermal alteration. We demonstrate that the compositional variation between melt particles of the suevitic rocks is the result of both incomplete homogenization of the target lithologies during impact and subsequent post‐impact hydrothermal alteration. Most melt particles are andesitic in composition. Clinopyroxene‐rich melt particles possess lower SiO₂ and higher CaO contents. These are interpreted by mixing of melts from the silicate basement with overlying carbonate rocks. Multi‐stage post‐impact hydrothermal alteration involved significant mass transfer of most major elements and caused further compositional heterogeneity between melt particles. Following backwash of seawater into the crater, palagonitization of glassy melt particles likely caused depletion of SiO₂, Al₂O₃, CaO, Na₂O, and enrichment of K₂O and FeO_tot during an early alteration stage. Since glass is very susceptible to fluid‐rock interaction, the state of primary crystallization of the melt particles had a significant influence on the intensity of the post‐impact hydrothermal mass transfer and was more pronounced in glassy melt particles than in well‐crystallized particles. In contrast to other occurrences of Chicxulub impactites, the Yax‐1 suevitic rocks show strong potassium metasomatism with hydrothermal K‐feldspar formation and whole rock K₂0 enrichment, especially in the lower unit of the suevitic sequence. A late stage of hydrothermal alteration is characterized by precipitation of silica, analcime, and Na‐bearing Mg‐rich smectite, among other minerals. This indicates a general evolution from a silica‐undersaturated fluid at relatively high potassium activities at an early stage toward a silica‐oversaturated fluid at relatively high sodium activities at later stages in the course of fluid rock interaction.     

Heavily metamorphosed clasts from the CV chondrite breccias Mokoia and Yamato‐86009

Abstract– Metamorphosed clasts in the CV carbonaceous chondrite breccias Mokoia and Yamato‐86009 (Y‐86009) are coarse‐grained, granular, polymineralic rocks composed of Ca‐bearing (up to 0.6 wt% CaO) ferroan olivine (Fa_34–39), ferroan Al‐diopside (Fs_9–13Wo_47–50, approximately 2–7 wt% Al₂O₃), plagioclase (An_37–84Ab_63–17), Cr‐spinel (Cr/(Cr + Al) = 0.19–0.45, Fe/(Fe + Mg) = 0.60–0.79), nepheline, pyrrhotite, pentlandite, Ca‐phosphate, and rare grains of Ni‐rich taenite; low‐Ca pyroxene is absent. Most clasts have triple junctions between silicate grains, indicative of prolonged thermal annealing. Based on the olivine‐spinel and pyroxene thermometry, the estimated metamorphic temperature recorded by the clasts is approximately 1100 K. Few clasts experienced thermal metamorphism to a lower degree and preserved chondrule‐like textures. The Mokoia and Y‐86009 clasts are mineralogically unique and different from metamorphosed chondrites of known groups (H, L, LL, R, EH, EL, CO, CK) and primitive achondrites (acapulcoites, brachinites, lodranites). On a three‐isotope oxygen diagram, compositions of olivine in the clasts plot along carbonaceous chondrite anhydrous mineral line and the Allende mass‐fractionation line, and overlap with those of the CV chondrule olivines; the Δ¹⁷O values of the clasts range from about ?4.3‰ to ?3.0‰. We suggest that the clasts represent fragments of the CV‐like material that experienced metasomatic alteration, high‐temperature metamorphism, and possibly melting in the interior of the CV parent asteroid. The lack of low‐Ca pyroxene in the clasts could be due to its replacement by ferroan olivine during iron‐alkali metasomatic alteration or by high‐Ca ferroan pyroxene during melting under oxidizing conditions.     

Early solar system aqueous activity: K isotope evidence from Allende

The alkali element K is moderately volatile and fluid mobile; thus, it can be influenced by both primary processes (evaporation and recondensation) in the solar nebula and secondary processes (thermal and aqueous alteration) in the parent body. Since these primary and secondary processes would induce different isotopic fractionations, K isotopes could become a potential tracer to distinguish them. Using recently developed methods with improved precision (0.05‰, 95% confidence interval), we systematically measured the K isotopic compositions and major/trace elemental compositions of chondritic components (18 chondrules, 3 CAIs, 2 matrices, and 5 bulks) in the carbonaceous chondrite fall Allende. Among all the components analyzed in this study, CAIs, which formed initially under high‐temperature conditions in the solar nebula and were dominated by nominally K‐free refractory minerals, have the highest K₂O content (average 0.53 wt%) and have K isotope compositions most enriched in heavy isotopes (δ⁴¹K: ?0.30 to ?0.25‰). Such an observation is consistent with previous petrologic studies that show CAIs in Allende have undergone alkali enrichment during metasomatism. In contrast, chondrules contain lower K₂O content (0.003–0.17 wt%) and generally lighter K isotope compositions (δ⁴¹K: ?0.87‰ to ?0.24‰). The matrix and bulks are nearly identical in K₂O content and K isotope compositions (0.02–0.05 wt%; δ⁴¹K: ?0.62 to ? 0.46‰), which are, as expected, right in the middle of CAIs and chondrules. This strongly indicates that most of the chondritic components of Allende suffered aqueous alteration and their K isotopic compositions are the ramification of Allende parent‐body processing instead of primary nebular signatures. Nevertheless, we propose the small K isotope fractionations observed (< 1‰) among Allende components are likely similar to the overall range of K isotopic fractionation that occurred in nebular environment. Furthermore, the K isotope compositions seen in the components of Allende in this study are consistent with MC‐ICP‐MS analyses of the components in ordinary chondrites, which also show an absence of large (10‰) isotope fractionations. This is not expected as evaporation experiments in nebular conditions suggest there should be large K isotopic fractionations. Nevertheless, possible nebular processes such as chondrules back exchanging with ambient gas when they formed could explain this lack of large K isotopic variation.     

Silica‐rich igneous rims around magnesian chondrules in CR carbonaceous chondrites: Evidence for condensation origin from fractionated nebular gas

Abstract— The outer portions of many type I chondrules (Fa and Fs <5 mol%) in CR chondrites (except Renazzo and Al Rais) consist of silica‐rich igneous rims (SIRs). The host chondrules are often layered and have a porphyritic core surrounded by a coarse‐grained igneous rim rich in low‐Ca pyroxene. The SIRs are sulfide‐free and consist of igneously‐zoned low‐Ca and high‐Ca pyroxenes, glassy mesostasis, Fe, Ni‐metal nodules, and a nearly pure SiO₂ phase. The high‐Ca pyroxenes in these rims are enriched in Cr (up to 3.5 wt% Cr₂O₃) and Mn (up to 4.4 wt% MnO) and depleted in Al and Ti relative to those in the host chondrules, and contain detectable Na (up to 0.2 wt% Na₂O). Mesostases show systematic compositional variations: Si, Na, K, and Mn contents increase, whereas Ca, Mg, Al, and Cr contents decrease from chondrule core, through pyroxene‐rich igneous rim (PIR), and to SIR; FeO content remains nearly constant. Glass melt inclusions in olivine phenocrysts in the chondrule cores have high Ca and Al, and low Si, with Na, K, and Mn contents that are below electron microprobe detection limits. Fe, Ni‐metal grains in SIRs are depleted in Ni and Co relative to those in the host chondrules. The presence of sulfide‐free, SIRs around sulfide‐free type I chondrules in CR chondrites may indicate that these chondrules formed at high (>800 K) ambient nebular temperatures and escaped remelting at lower ambient temperatures. We suggest that these rims formed either by gas‐solid condensation of silica‐normative materials onto chondrule surfaces and subsequent incomplete melting, or by direct SiO_(gas) condensation into chondrule melts. In either case, the condensation occurred from a fractionated, nebular gas enriched in Si, Na, K, Mn, and Cr relative to Mg. The fractionation of these lithophile elements could be due to isolation (in the chondrules) of the higher temperature condensates from reaction with the nebular gas or to evaporation‐recondensation of these elements during chondrule formation. These mechanisms and the observed increase in pyroxene/olivine ratio toward the peripheries of most type I chondrules in CR, CV, and ordinary chondrites may explain the origin of olivine‐rich and pyroxene‐rich chondrules in general.     

Complexly zoned chromium‐aluminum spinel found in situ in the Allende meteorite

Abstract— In addition to the Mg‐, Al‐, ¹⁶O‐rich spinels that are known to occur in refractory inclusions, the Murchison meteorite contains Cr‐rich, ¹⁶O‐poor spinels, most of whose sources are unknown because they are rarely found in situ. Here we report the in situ occurrence in Allende of Cr‐rich spinels, found in 13 chondrules and 4 “olivine‐rich objects”. The Allende spinels exhibit major and minor element contents, isotopic compositions, and zoning of Cr₂O₃ contents like those of the Cr‐spinels from Murchison. Some chondrules contain patchy‐zoned spinel (Simon et al., 1994), which suggests that such grains did not form by sintering but perhaps by formation of overgrowths on relic grains. Unlike the olivine‐rich objects, phases in all three chondrules that were analyzed by ion microprobe have uniform, near‐normal O‐isotopic compositions. One olivine‐rich object, ALSP1, has a huge (1 mm) fragment of chevron‐zoned spinel. This spinel has near‐normal O‐isotopic compositions that are quite distinct from those of adjacent forsteritic olivine, which are relatively ¹⁶O‐rich and plot on the calcium‐aluminum‐inclusion (CAI) line, like some isolated forsterite grains found in Allende. The spinel and olivine in this object are therefore not genetically related to each other. Another olivine‐rich object, ALSP11A, contains a rectangular, 150 ×s 100 μm, homogeneous spinel grain with 50 wt% Cr₂O₃ and 23 wt% FeO in a vuggy aggregate of finer‐grained (5–90 μm), FeO‐rich (Fo_47–55) olivine. The magnesian core of one olivine grain has a somewhat ¹⁶O‐rich isotopic composition like that of the large spinel, whereas the FeO‐rich olivine is relatively ¹⁶O‐poor. The composition of the spinel in ALSP11A plots on the CAI line, the first Cr‐rich spinel found to do so. Chevron‐zoned spinel has not been observed in chondrules, and it is unlikely that either ALSP1 or ALSP11A were ever molten. Calculations show that a spinel with the composition of that in ALSP1 can condense at 1780 K at a P^tot of 10^?3 atm and a dust/gas ratio of 100 relative to solar. The Cr‐rich spinel in ALSP11A could condense at ～1420 K, but this would require a dust/gas enrichment of 1000 relative to solar. The data presented here confirm that, as in Murchison, the coarse Cr‐rich spinels in Allende are relatively ¹⁶O‐depleted and are isotopically distinct from the ¹⁶O‐enriched MgAl₂O₄ from CAIs. Sample ALSP11A may represent a third population, one that is Cr‐rich and plots on the CAI line. That the O‐isotopic composition of ALSP1 is like those of Cr‐rich spinels from chondrules indicates that O‐isotopic compositions cannot be used to distinguish whether grains from such unequilibrated objects are condensates or are fragments from a previous generation of chondrules.     

Origin of a metamorphosed lithic clast in CM chondrite Grove Mountains 021536

Abstract– A metamorphosed lithic clast was discovered in the CM chondrite Grove Mountains 021536, which was collected in the Antarctica by the Chinese Antarctic Research Exploration team. The lithic clast is composed mainly of Fe‐rich olivine (Fo₆₂) with minor diopside (Fs_9.7–11.1Wo_48.3–51.6), plagioclase (An_43–46.5), nepheline, merrillite, Al‐rich chromite (21.8 wt% Al₂O₃; 4.43 wt% TiO₂), and pentlandite. Δ¹⁷O values of olivine in the lithic clast vary from ?3.9‰ to ?0.8‰. Mineral compositions and oxygen isotopic compositions of olivine suggest that the lithic clast has an exotic source different from the CM chondrite parent body. The clast could be derived from strong thermal metamorphism of pre‐existing chondrule that has experienced low‐temperature anhydrous alteration. The lithic clast is similar in mineral assemblage and chemistry to a few clasts observed in oxidized CV3 chondrites (Mokoia and Yamato‐86009) and might have been derived from the interior of the primitive CV asteroid. The apparent lack of hydration in the lithic clast indicates that the clast accreted into the CM chondrite after hydration of the CM components.     

Origin of tektites

Abstract— The origin of tektites has been obscure because of the following dilemma. The application of physical principles to the data available on tektites points strongly to origin from one or more lunar volcanoes; but few glasses of tektite composition have hitherto been reported from the lunar samples. Instead, the lunar silicic glasses consist chiefly of a material very rich in K₂O and poor in MgO. The ratio of K₂O/MgO is higher in these glasses than in any tektites reported. The solution of the dilemma seems to come from the study of some recently discovered terrestrial deposits of tektite glass with high values of K₂O/MgO at the Cretaceous-Tertiary boundary. These glasses are found to be very vulnerable to crystallization into sandine or to alteration to smectite. These end products are known and are more abundant than any terrestrial deposits of tektite glass. It seems possible that, in fact, the moon produces tektite glass, mostly of the high K₂O-low MgO type; but on Earth these deposits are destroyed. The much less abundant deposits with lower K and higher Mg are observed because they survive. Other objections to the lunar origin hypothesis appear to be answerable.     

K2O‐rich trapped melt in olivine in the Nakhla meteorite: Implications for petrogenesis of nakhlites and evolution of the Martian mantle

We used new analytical and theoretical methods to determine the major and minor element compositions of the primary trapped liquid (PTLs) represented by melt inclusions in olivine and augite in the Martian clinopyroxenite, Nakhla, for comparison with previously proposed compositions for the Nakhla (or nakhlite) parent magma. We particularly focused on obtaining accurate K₂O contents, and on testing whether high K₂O contents and K₂O/Na₂O ratios obtained in previous studies of melt inclusions in olivine in Nakhla could have been due to unrepresentative sampling, systematic errors arising from electron microprobe techniques, late alteration of the inclusions, and/or boundary layer effects. Based on analyses of 35 melt inclusions in olivine cores, the PTL in olivine, PTL_oliv, contained (by wt) approximately 47% SiO₂, 6.3% Al₂O₃, 9.6% CaO, 1.8% K₂O, and 0.9% Na₂O, with K₂O/Na₂O = 2.0. We infer that the high K₂O content of PTL_oliv is not due to boundary layer effects and represents a real property of the melt from which the host olivine crystallized. This melt was cosaturated with olivine and augite. Its mg# is model‐dependent and is constrained only to be ≥19 (equilibrium Fo = 40). Based on analyses of 91 melt inclusions in augite cores, the PTL in augite, PTL_aug, contained (by wt) 53–54% SiO₂, 7–8% Al₂O₃, 0.8–1.1% K₂O, and 1.1–1.4% Na₂O, with K₂O/Na₂O = 0.7–0.8. This K₂O content and K₂O/Na₂O ratio are significantly higher than inferred in studies of melt inclusions in augite in Nakhla by experimental rehomogenization. PTL_aug was saturated only with augite, and in equilibrium with augite cores of mg# 62. PTL_aug represents the Nakhla parent magma, and does not evolve to PTL_oliv by fractional crystallization. We therefore conclude that olivine cores in Nakhla (and, by extension, other nakhlites) are xenocrystic. We propose that PTL_oliv and PTL_aug were generated from the same source region. PTL_oliv was generated first and emplaced to form olivine‐rich cumulate rocks. Shortly thereafter, PTL_aug was generated and ascended through these olivine‐rich cumulates, incorporating fragments of wallrock that became the xenocrystic olivine cores in Nakhla. The Nakhla (nakhlite) mantle source region was pyroxenitic with some olivine, and could have become enriched in K relative to Na via metasomatism. A high degree of melting of this source produced the silica‐poor, alkali‐rich magma PTL_oliv. Further ascension and decompression of the source led to generation of the silica‐rich, relatively alkali‐poor magma PTL_aug. Potassium‐rich magmas like those involved in the formation of the nakhlites represent an important part of the diversity of Martian igneous rocks.     

Alkali‐feldspathic material entrained in Fe,S‐rich veins in a monomict ureilite

Abstract— The Elephant Moraine (EET) 96001 ureilite contains a remarkable diversity of feldspars, which occur as tiny (no more than 60 μm maximum dimension) grains within a few Fe,S‐rich (now weathered to mostly Fe oxide) veins. Molar S: Fe ratio in the veins averages 0.08 ± 0.02. The veins meander and feature large fluctuations in apparent width; they appear to have entered this monomict breccia by a gentle, percolative process, not by violent impact injection. The feldspars are accompanied by a diverse suite of K‐rich (and generally also Ti‐rich) feldspathic glasses, and also major proportions of silica and pyroxene, which is largely fassaitic. A rhönite‐like phase is also found, and, as inclusions in one of the fassaites, a Cr‐poor spinel‐like phase. The feldspars mostly feature remarkably high K/Na compared to feldspars of comparable An from polymict ureilites. The EET 96001 feldspathic component was probably once part of a thin basaltic crust on a ureilite asteroid. The spinel included in one of the fassaites formed at remarkably high f0₂ (apparent oxidation state of iron: ～41 atom% Fe³⁺), suggesting that the parent magma possibly assimilated near‐surface water (however, the Fe³⁺ was not directly measured, and has conceivably been affected by terrestrial weathering; also, there is no assurance that this fassaite originated together with the typical feldspar). We speculate that the feldspathic component was mixed into the dense, Fe,S‐rich vein material, and very soon thereafter the Fe,S‐rich vein material was emplaced adjacent to the EET 96001 host ureilite, at an advanced stage in a chaotic catastrophic disruption and partial reassembly process that affected all ureilites. The high‐K nature of the EET 96001 feldspathic component, including the feldspathic glasses, suggests that fractional fusion may not have been as common during ureilite anatexis as has been inferred from recent studies of clast assemblages in polymict ureilites.     

The regolith portion of the lunar meteorite Sayh al Uhaymir 169

Abstract— –Sayh al Uhaymir (SaU) 169 is a composite lunar meteorite from Oman that consists of polymict regolith breccia (8.44 ppm Th), adhering to impact‐melt breccia (IMB; 32.7 ppm Th). In this contribution we consider the regolith breccia portion of SaU 169, and demonstrate that it is composed of two generations representing two formation stages, labeled II and III. The regolith breccia also contains the following clasts: Ti‐poor to Ti‐rich basalts, gabbros to granulites, and incorporated regolith breccias. The average SaU 169 regolith breccia bulk composition lies within the range of Apollo 12 and 14 soil and regolith breccias, with the closest correspondence being with that of Apollo 14, but Sc contents indicate a higher portion of mare basalts. This is supported by relations between Sm‐Al₂O₃, FeO‐Cr₂O₃‐TiO₂, Sm/Eu and Th‐K₂O. The composition can best be modeled as a mixture of high‐K KREEP, mare basalt and norite/troctolite, consistent with the rareness of anorthositic rocks. The largest KREEP breccia clast in the regolith is identical in its chemical composition and total REE content to the incompatible trace‐element (ITE)‐ rich high‐K KREEP rocks of the Apollo 14 landing site, pointing to a similar source. In contrast to Apollo 14 soil, SaU 169 IMB and SaU 169 KREEP breccia clast, the SaU 169 regolith is not depleted in K/Th, indicating a low contribution of high‐Th IMB such as the SaU 169 main lithology in the regolith. The data presented here indicate the SaU 169 regolith breccia is from the lunar front side, and has a strong Procellarum KREEP Terrane signature.     

The Gao‐Guenie impact melt breccia—Sampling a rapidly cooled impact melt dike on an H chondrite asteroid?

The Gao‐Guenie H5 chondrite that fell on Burkina Faso (March 1960) has portions that were impact‐melted on an H chondrite asteroid at ~300 Ma and, through later impact events in space, sent into an Earth‐crossing orbit. This article presents a petrographic and electron microprobe analysis of a representative sample of the Gao‐Guenie impact melt breccia consisting of a chondritic clast domain, quenched melt in contact with chondritic clasts, and an igneous‐textured impact melt domain. Olivine is predominantly Fo_80–82. The clast domain contains low‐Ca pyroxene. Impact melt‐grown pyroxene is commonly zoned from low‐Ca pyroxene in cores to pigeonite and augite in rims. Metal–troilite orbs in the impact melt domain measure up to ~2 mm across. The cores of metal orbs in the impact melt domain contain ~7.9 wt% of Ni and are typically surrounded by taenite and Ni‐rich troilite. The metallography of metal–troilite droplets suggest a stage I cooling rate of order 10 °C s^?1 for the superheated impact melt. The subsolidus stage II cooling rate for the impact melt breccia could not be determined directly, but was presumably fast. An analogy between the Ni rim gradients in metal of the Gao‐Guenie impact melt breccia and the impact‐melted H6 chondrite Orvinio suggests similar cooling rates, probably on the order of ~5000–40,000 °C yr^?1. A simple model of conductive heat transfer shows that the Gao‐Guenie impact melt breccia may have formed in a melt injection dike ~0.5–5 m in width, generated during a sizeable impact event on the H chondrite parent asteroid.     

Major and trace element compositions of georgiaites: Clues to the source of North American tektites

Abstract— Electron microprobe and laser ablation, inductively‐coupled plasma mass spectrometer analyses of 24 georgiaites show that these tektites are all Si‐rich (79–83 wt% SiO₂) glasses with variable major and trace element abundances (e.g., FeO varies from 2.1 to 3.7 wt%). Glass compositions are similar to but not identical with average upper continental crust. For example, georgiaites are light rare earth element enriched with small negative Eu anomalies (Eu/Eu*=0.73‐0.86) and La‐Th‐Sc systematics are intermediate between that of Archean and post‐Archean continental crust. When the georgiaite data are placed in the context of data for all North American tektites, triangular arrays appear on some oxide‐oxide plots (e.g., FeO‐MgO). Large variations in refractory element abundances and ratios compared to the variation in SiO₂ favors mixing over volatilization as a cause of the compositional variation. If all the tektites formed as a result of a single impact, then triangular arrays in oxide‐oxide variation diagrams require at least three source components. These components include a Si‐rich material, probably a quartz‐rich sand that was predominant in the formation of georgiaites. Two relatively silica‐poor and Fe‐rich components have compositional characteristics similar to shales and greywackes. The La‐Th‐Sc systematics of the georgiaites and most other North American tektites are distinctive and could potentially be used to link the tektites to Eocene sediments at the Chesapeake Bay impact structure.     

Frontier Mountain 93001: A coarse‐grained,enstatite‐augite‐oligoclase‐rich,igneous rock from the acapulcoite‐lodranite parent asteroid

Abstract— The Frontier Mountain (FRO) 93001 meteorite is a 4.86 g fragment of an unshocked, medium‐ to coarse‐grained rock from the acapulcoite‐lodranite (AL) parent body. It consists of anhedral orthoenstatite (Fs_{13.3 ± 0.4}Wo_{3.1 ± 0.2}), augite (Fs_{6.1 ± 0.7}Wo_{42.3 ± 0.9}; Cr₂O₃ = 1.54 ± 0.03), and oligoclase (Ab_{80.5 ± 3.3}Or_{3.1 ± 0.6}) up to >1 cm in size enclosing polycrystalline aggregates of fine‐grained olivine (average grain size: 460 ± 210 μm) showing granoblastic textures, often associated with Fe,Ni metal, troilite, chromite (cr# = 0.91 ± 0.03; fe# = 0.62 ± 0.04), schreibersite, and phosphates. Such aggregates appear to have been corroded by a melt. They are interpreted as lodranitic xenoliths. After the igneous (the term “igneous” is used here strictly to describe rocks or minerals that solidified from molten material) lithology intruding an acapulcoite host in Lewis Cliff (LEW) 86220, FRO 93001 is the second‐known silicate‐rich melt from the AL parent asteroid. Despite some similarities, the silicate igneous component of FRO 93001 (i.e., the pyroxene‐plagioclase mineral assemblage) differs in being coarser‐grained and containing abundant enstatite. Melting‐crystallization modeling suggests that FRO 93001 formed through high‐degree partial melting (≥35 wt%; namely, ≥15 wt% silicate melting and ?20 wt% metal melting) of an acapulcoitic source rock, or its chondritic precursor, at temperatures ≥1200 °C, under reducing conditions. The resulting magnesium‐rich silicate melt then underwent equilibrium crystallization; prior to complete crystallization at ?1040 °C, it incorporated lodranitic xenoliths. FRO 93001 is the highest‐temperature melt from the AL parent‐body so far available in laboratory. The fact that FRO 93001 could form by partial melting and crystallization under equilibrium conditions, coupled with the lack of quench‐textures and evidence for shock deformation in the xenoliths, suggests that FRO 93001 is a magmatic rock produced by endogenic heating rather than impact melting.     

Petrology of silicate inclusions in the Sombrerete ungrouped iron meteorite: Implications for the origins of IIE‐type silicate‐bearing irons

Abstract— The petrography and mineral and bulk chemistries of silicate inclusions in Sombrerete, an ungrouped iron that is one of the most phosphate‐rich meteorites known, was studied using optical, scanning electron microscopy (SEM), electron microprobe analysis (EMPA), and secondary ion mass spectrometry (SIMS) techniques. Inclusions contain variable proportions of alkalic siliceous glass (?69 vol% of inclusions on average), aluminous orthopyroxene (?9%, Wo_1–4Fs_25–35, up to ?3 wt% Al), plagioclase (?8%, mainly An_70–92), Cl‐apatite (?7%), chromite (?4%), yagiite (?1%), phosphate‐rich segregations (?1%), ilmenite, and merrillite. Ytterbium and Sm anomalies are sometimes present in various phases (positive anomalies for phosphates, negative for glass and orthopyroxene), which possibly reflect phosphate‐melt‐gas partitioning under transient, reducing conditions at high temperatures. Phosphate‐rich segregations and different alkalic glasses (K‐rich and Na‐rich) formed by two types of liquid immiscibility. Yagiite, a K‐Mg silicate previously found in the Colomera (IIE) iron, appears to have formed as a late‐stage crystallization product, possibly aided by Na‐K liquid unmixing. Trace‐element phase compositions reflect fractional crystallization of a single liquid composition that originated by low‐degree (?4–8%) equilibrium partial melting of a chondritic precursor. Compositional differences between inclusions appear to have originated as a result of a “filter‐press differentiation” process, in which liquidus crystals of Cl‐apatite and orthopyroxene were less able than silicate melt to flow through the metallic host between inclusions. This process enabled a phosphoran basaltic andesite precursor liquid to differentiate within the metallic host, yielding a dacite composition for some inclusions. Solidification was relatively rapid, but not so fast as to prevent flow and immiscibility phenomena. Sombrerete originated near a cooling surface in the parent body during rapid, probably impact‐induced, mixing of metallic and silicate liquids. We suggest that Sombrerete formed when a planetesimal undergoing endogenic differentiation was collisionally disrupted, possibly in a breakup and reassembly event. Simultaneous endogenic heating and impact processes may have widely affected silicate‐bearing irons and other solar system matter.     

Experimental constraints on alkali condensation in chondrule formation

Abstract— To assess whether the alkali behavior observed in chondrules of primitive meteorites is attributable to volatilization from the raw materials of chondrules during chondrule formation events or attributable to condensation processes from the nebular gas, we set up a new experimental device able to expose silicate melt samples to a controlled alkali partial pressure at high temperature under fixed O fugacity. Using a mixture of potassium carbonate (K₂CO₃) and graphite (C) as the source of the K gas (K_g), we studied the condensation kinetics of K and its solubility in CaO‐MgO‐Al₂O₃‐SiO₂ silicate melts, according to the reaction 2 K _(g) + 1/2 _(g) = K₂O _(melt) From these results, we show that alkali entering in chondrules from the nebular gas is a viable mechanism to explain the chondrules alkali contents and their δ⁴¹K‐isotopic signatures, at timescales relevant to chondrule formation. Finally, we also suggest that chondrules may have formed in non‐canonical nebular environments and that the flash‐heating scenario is not a prerequisite to chondrule formation.     

Libyan Desert Glass: New field and Fourier transform infrared data

Results are presented of new geological observations and laboratory analyses on Libyan Desert Glass (LDG), a unique kind of impact glass found in Egypt, probably 28.5–29.4 million years in age. A new LDG occurrence has been discovered some 50 km southward of the main LDG occurrences in the Great Sand Sea. From Fourier transform infrared (FTIR) analysis, the molecular structure of LDG is refined and significant differences are shown between LDG specimens and other pure silica glasses (fulgurite, industrial fused quartz, and amorphous biogenic silica) that are related to differences in their structures. The slight variations observed here for the mean Si‐O‐Si angle between the different glasses are attributed to their thermal histories. With regard to the other glasses analyzed, the LDG infrared spectral parameters point to a higher ratio of discontinuities and defects in the tetrahedral (SiO₄) network. The quantitative mineralogical constitutions of sandstones and quartzites from the LDG geological setting were analyzed by FTIR. Cretaceous sandstones have a specific composition (about 90 wt% quartz, 10% dickite), clearly different from the Paleozoic ones (about 90 wt% quartz, but ≥7% kaolinite). It is shown that the reddish silts bearing the LDG are constituted mainly of microquartz enriched with dickite, whose particle size distribution is characteristic of fluvio‐lacustrine deposits, probably Oligocene to Miocene in age. The target rocks, most probably quartz sand, resulted from the weathering (loss of the cementing microquartz) of the Cretaceous sandstones from the Gilf Khebir Plateau with deposition in a high‐energy environment.     

Mars regolith versus SNC meteorites: Possible evidence for abundant crustal carbonates

Viking XRF analyses of the Martian regolith are compared with typical igneous rocks of the Earth, the Moon, the eucrite parent asteroid, and especially the shergottites, nakhlites, and Chassigny (SNC) meteorites, which are suspected to be basalts and mafic cumulates from Mars. A striking feature of the Martian regolith, compared to igneous rocks with similar molar (Mg + Fe)/Si ratios, is its extraordinarily low Ca/Si ratio. The regolith's low Ca/Si ratio is probably not a result of simple mixing (isochemical weathering) of SNC-like rocks with other igneous rocks, unless the regolith contains a large component of rock with an improbable combination of extremely low Ca/Si and (Mg + Fe)/Si, and yet low K₂O and Zr. Several other models might conceivably account for the low Ca/Si ratio, but I suggest that most of the “missing” Ca was removed from the regolith as Ca-carbonate. Formation of a mass of carbonate equivalent to a global shell 20 m thick would suffice to remove 1000 mbar of CO₂ from the Martian atmosphere. Thus, the peculiar Ca/Si ratio of the Martian regolith tends to support the hypothesis that the climate of Mars was once far warmer and wetter than it is today.     

Geochemistry and shock petrography of the Crow Creek Member,South Dakota,USA: Ejecta from the 74‐Ma Manson impact structure

Abstract— The Crow Creek Member is one of several marl units recognized within the Upper Cretaceous Pierre Shale Formation of eastern South Dakota and northeastern Nebraska, but it is the only unit that contains shock‐metamorphosed minerals. The shocked minerals represent impact ejecta from the 74‐Ma Manson impact structure (MIS). This study was aimed at determining the bulk chemical compositions and analysis of planar deformation features (PDFs) of shocked quartz; for the basal and marly units of the Crow Creek Member. We studied samples from the Gregory 84‐21 core, Iroquois core and Wakonda lime quarry. Contents of siderophile elements are generally high, but due to uncertainties in the determination of Ir and uncertainties in compositional sources for Cr, Co, and Ni, we could not confirm an extraterrestrial component in the Crow Creek Member. We recovered several shocked quartz grains from basal‐unit samples, mainly from the Gregory 84‐21 core, and results of PDF measurements indicate shock pressures of at least 15 GPa. All the samples are composed chiefly of SiO₂ (29–58 wt%), Al₂O₃ (6–14 wt%), and CaO (7–30 wt%). When compared to the composition of North American Shale Composite, the samples are significantly enriched in CaO, P₂O₅, Mn, Sr, Y, U, Cr, and Ni. The contents of rare earth elements (REE), high field strength elements (HFSE), Cr, Co, Sc, and their ratios and chemical weathering trends, reflect both felsic and basic sources for the Crow Creek Member, an inference, which is consistent with the lithological compositions in the environs of the MIS. The high chemical indices of alteration and weathering (CIA' and CIW': 75–99), coupled with the Al₂O₃‐(CaO*+Na₂O)‐K₂O (A‐CN'‐K) ratios, indicate that the Crow Creek Member and source rocks had undergone high degrees of chemical weathering. The expected ejecta thicknesses at the sampled locations (409 to 219 km from Manson) were calculated to range from about 1.9 to 12.2 cm (for the present‐day crater radius of Manson), or 0.4 to 2.4 cm (for the estimated transient cavity radius). The trend agrees with the observed thicknesses of the basal unit of the Crow Creek Member, but the actually observed thicknesses are larger than the calculated ones, indicating that not all of the basal unit comprises impact ejecta.