Geochemical and petrographic characteristics of impactites and Cretaceous target rocks from the Yaxcopoil‐1 borehole,Chicxulub impact structure,Mexico: Implications for target composition

Abstract— We present major and trace element data as well as petrographic observations for impactites (suevitic groundmass, bulk suevite, and melt rock particles) and target lithologies, including Cretaceous anhydrite, dolomite, argillaceous limestone, and oil shale, from the Yaxcopoil‐1 borehole, Chixculub impact structure. The suevitic groundmass and bulk suevite have similar compositions, largely representing mixtures of carbonate and silicate components. The latter are dominated by melt rock particles. Trace element data indicate that dolomitic rocks represented a significant target component that became incorporated into the suevites; in contrast, major elements indicate a strong calcitic component in the impactites. The siliceous end‐member requires a mafic component in order to explain the low SiO₂ content. Multicomponent mixing of various target rocks, the high alteration state, and dilution by carbonate complicate the determination of primary melt particle compositions. However, two overlapping compositional groups can be discerned—a high‐Ba, low‐Ta group and a high‐Fe, high‐Zn, and high‐Hf group. Cretaceous dolomitic rocks, argillaceous limestone, and shale are typically enriched in U, As, Br, and Sb, whereas anhydrite contains high Sr contents. The oil shale samples have abundances that are similar to the North American Shale Composite (NASC), but with a comparatively high U content. Clastic sedimentary rocks are characterized by relatively high Th, Hf, Zr, As, and Sb abundances. Petrographic observations indicate that the Cretaceous rocks in the Yaxcopoil‐1 drill core likely register a multistage deformation history that spans the period from pre‐ to post‐impact. Contrary to previous studies that claimed evidence for the presence of impact melt breccia injection veins, we have found no evidence in our samples from a depth of 1347–1348 m for the presence of melt breccia. We favor that clastic veinlets occur in a sheared and altered zone that underwent intense diagenetic overprint prior to the impact event.     

Heterogeneity of melts in impact deposits and implications for their origin (Ries suevite,Germany)

Impact melt‐bearing clastic deposits (suevites) are one of the most important records of the impact cratering process. A deeper understanding of their composition and formation is therefore essential. This study focuses on impact melt particles in suevite at Ries, Germany. Textures and chemical evidence indicate that the suevite contains three melt types that originate from different shock levels in the target. The most abundant melt type (“melt type 1”) represents well‐mixed whole‐rock melting of crystalline basement and includes incompletely mixed mafic melt schlieren (“melt type 1 mafic”). Polymineralic melt type 2 comprises mixes between monomineralic melt types 3 and melt type 1. Melt types 2 and 3 are located within melt type 1 as small patches or schlieren but also isolated within the suevite matrix. The main melt type 1 is heterogeneous with respect to trace elements, varying geographically around the crater: in the western sector, it has lower values in trace elements, e.g., Ba, Zr, Th, and Ce, than in the eastern sector. The west–east zoning likely reflects the heterogeneous nature of crystalline basement target rocks with lower trace element contents, e.g., Ba, Zr, Th, and Ce, in the west compared to the east. The chemical zoning pattern of suevite melt type 1 indicates that mixing during ejection and emplacement occurred only on a local (hundreds of meters) scale. The incomplete larger scale mixing indicated by the preservation of these local chemical signatures, and schlieren corroborate the assumption that mixing, ejection, and quenching were very rapid, short‐lived processes.     

Melt in the impact breccias from the Eyreville drill cores,Chesapeake Bay impact structure,USA

The center of the 35.3 Ma Chesapeake Bay impact structure (85 km diameter) was drilled during 2005/2006 in an ICDP–USGS drilling project. The Eyreville drill cores include polymict impact breccias and associated rocks (1397–1551 m depth). Tens of melt particles from these impactites were studied by optical and electron microscopy, electron microprobe, and microRaman spectroscopy, and classified into six groups: m1—clear or brownish melt, m2—brownish melt altered to phyllosilicates, m3—colorless silica melt, m4—melt with pyroxene and plagioclase crystallites, m5—dark brown melt, and m6—melt with globular texture. These melt types have partly overlapping major element abundances, and large compositional variations due to the presence of schlieren, poorly mixed melt phases, partly digested clasts, and variable crystallization and alteration. The different melt types also vary in their abundance with depth in the drill core. Based on the chemical data, mixing calculations were performed to determine possible precursors of these melt particles. The calculations suggest that most melt types formed mainly from the thick sedimentary section of the target sequence (mainly the Potomac Formation), but an additional crystalline basement (schist/gneiss) precursor is likely for the most abundant melt types m2 and m5. Sedimentary rocks with compositions similar to those of the melt particles are present among the Eyreville core samples. Therefore, sedimentary target rocks were the main precursor of the Eyreville melt particles. However, the composition of the melt particles is not only the result of the precursor composition but also the result of changes during melting and solidification, as well as postimpact alteration, which must also be considered. The variability of the melt particle compositions reflects the variety of target rocks and indicates that there was no uniform melt source. Original heterogeneities, resulting from melting of different target rocks, may be preserved in impactites of some large impact structures that formed in volatile‐rich targets, because no large melt body exists, in which homogenization would have taken place.     

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.     

Incipient devitrification of impact melt particles at Bosumtwi crater,Ghana: Implications for suevite cooling history and melt dispersion

The petrographic, mineralogical, and geochemical compositions of the incipient devitrification products in impact melt fragments found in outer suevites at the Bosumtwi impact crater were studied to reconstruct the postimpact environmental constraints on the suevite formation and to refine its cooling history. Our study shows that devitrified melt/particles contain numerous microlitic crystals and crystal aggregates of different shapes derived from rapid cooling. The matrix of melt/particles in Bosumtwi suevites contains abundant Mg‐hercynite (pleonaste)‐type spinels with sizes rarely exceeding a few micrometers. High nucleation density of microlites suggests rapid crystallization under strong undercooling in the presence of abundant volatiles. Although the Bosumtwi impact event took place in a continental environment, the possible sources for elevated fluid/volatile content could have been the groundwater in the deeply weathered and fractured‐jointed Birimian basement, dewatering of abundant hydrous phases in weathered crust or hydrothermally altered basement, and the shale/phyllite–greywacke lithologies in the target rocks. Our results show that enough volatiles were present in the target rocks at the time of impact for the effective impact melt dispersion observed in Bosumtwi impactites.     

Glass‐bearing inclusions in Shergotty and Chassigny: Consistent samples of a primary trapped melt?

Glass‐bearing inclusions hosted by different mineral phases in SNC meteorites provide important information on the conditions that prevailed during formation of early phases and/or on the composition of the primary trapped liquids/melts of these rocks. Although extensive previous work has been reported on such inclusions, several questions are still unresolved. We performed a chemical and petrographic study of the constituents (glasses and mineral assemblage) of glassy and multiphase inclusions in Shergotty and Chassigny. We focused on obtaining accurate trace element contents of glasses and co‐existing minerals and discussing their highly variable REE contents. Our results reveal an unusual geochemistry of trace element contents that appear to be independent of their major element compositions. Chemical equilibrium between phases inside inclusions as well as between glasses and host minerals could not be established. The LREE contents of glasses in glass inclusions can vary by up to two orders of magnitude. The depletion in trace element abundances shown by glasses seem to be inconsistent with these phases being residual melts. The light lithophile element contents of glasses are highly variable with enrichment in incompatible elements (e.g., Be, Sr, Ba, and LREE) indicating some processes involving percolation of fluids. All of these features are incompatible with glass‐bearing inclusions in the host minerals acting as closed systems preserving unmodified primary liquids/melts. Glass‐bearing inclusions in Shergotty and Chassigny appear to have been altered (as was the rock itself) by different postformational processes (e.g., shock, metamorphism, metasomatic [?] fluids) that affected these meteorites with different degree of intensity. Our results indicate that these inclusions could not preserve a reliable sample of the primary trapped melt.     

Target rocks,impact glasses,and melt rocks from the Lonar impact crater,India: Petrography and geochemistry

Abstract— The Lonar crater, India, is the only well‐preserved simple crater on Earth in continental flood basalts; it is excavated in the Deccan trap basalts of Cretaceous‐Tertiary age. A representative set of target basalts, including the basalt flows excavated by the crater, and a variety of impact breccias and impact glasses, were analyzed for their major and trace element compositions. Impact glasses and breccias were found inside and outside the crater rim in a variety of morphological forms and shapes. Comparable geochemical patterns of immobile elements (e.g., REEs) for glass, melt rock and basalt indicates minimal fractionation between the target rocks and the impactites. We found only little indication of post‐impact hydrothermal alteration in terms of volatile trace element changes. No clear indication of an extraterrestrial component was found in any of our breccias and impact glasses, indicating either a low level of contamination, or a non‐chondritic or otherwise iridium‐poor impactor.     

Petrographic studies of the impact melts from Meteor Crater,Arizona, USA

Abstract— We investigated the ballistically dispersed melts from Meteor Crater, Arizona, USA to determine the stratigraphic extent of its melt zone from the compositional relationship of melts and target rocks. Most melt particles are crystallized, hydrated, and oxidized; pristine glasses are rare. Hydration and oxidation occurred at ambient temperatures long after the impact. The preserved glasses are generally clear and texturally homogeneous, but unlike typical impact melts, they have unusually heterogeneous compositions, both within individual particles and from sample to sample. For example, the average SiO₂ for individual particles ranges from 43 to 65%. The projectile content is unusually high and it is distributed bimodally, with specific samples containing either 5–10% or 20–30% FeO. These compositional heterogeneities most likely reflect the high carbonate content of the target rocks and the release of copious CO₂ that dispersed the melts, thereby terminating melt flow and mixing. The high projectile content and the CO₂ depleted residue of purely sedimentary rocks produced mafic melts that crystallized fine‐grained olivine and pyroxene. The melts fall into three compositional groups reflecting variable proportions of the major target formations, Moenkopi, Kaibab, and Coconino. Least‐square mixing calculations revealed one group to contain 55% Moenkopi, 40% quartz‐rich, upper Kaibab, and 5% meteorite, suggesting a source depth of <30 m from the pre‐impact surface. The other two melt groups have higher contents of meteorite (15–20%) and Kaibab (50–70%) and contain more SiO₂ than average Kaibab. The additional quartz may have been derived from Coconino or the upper Kaibab, implying melt depths >90 m or <30 m, respectively. Additional studies, especially hydrocode calculations, are needed to better understand the source depth of these melts and their exceptionally high projectile content.     

A petrogenetic model for the origin and compositional variation of the martian basaltic meteorites

Abstract— The major element, trace element, and isotopic compositional ranges of the martian basaltic meteorite source regions have been modeled assuming that planetary differentiation resulted from crystallization of a magma ocean. The models are based on low to high pressure phase relationships estimated from experimental runs and estimates of the composition of silicate Mars from the literature. These models attempt to constrain the mechanisms by which the martian meteorites obtained their superchondritic CaO/Al₂O₃ ratios and their source regions obtained their parent/daughter (⁸⁷Rb/⁸⁶Sr, ¹⁴⁷Sm/¹⁴⁴Nd, and ¹⁷⁶Lu/¹⁷⁷Hf) ratios calculated from the initial Sr, Nd, and Hf isotopic compositions of the meteorites. High pressure experiments suggest that majoritic garnet is the liquidus phase for Mars relevant compositions at or above 12 GPa. Early crystallization of this phase from a martian magma ocean yields a liquid characterized by an elevated CaO/Al₂O₃ ratio and a high Mg#. Olivine‐pyroxene‐garnet‐dominated cumulates that crystallize subsequently will also be characterized by superchondritic CaO/Al₂O₃ ratios. Melting of these cumulates yields liquids with major element compositions that are similar to calculated parental melts of the martian meteorites. Furthermore, crystallization models demonstrate that some of these cumulates have parent/daughter ratios that are similar to those calculated for the most incompatible‐element‐depleted source region (i.e., that of the meteorite Queen Alexandra [QUE] 94201). The incompatible‐element abundances of the most depleted (QUE 94201‐like) source region have also been calculated and provide an estimate of the composition of depleted martian mantle. The incompatible‐element pattern of depleted martian mantle calculated here is very similar to the pattern estimated for depleted Earth's mantle. Melting the depleted martian mantle composition reproduces the abundances of many incompatible elements in the parental melt of QUE 94201 (e.g., Ba, Th, K, P, Hf, Zr, and heavy rare earth elements) fairly well but does not reproduce the abundances of Rb, U, Ta and light rare earth elements. The source regions for meteorites such as Shergotty are successfully modeled as mixtures of depleted martian mantle and a late stage liquid trapped in the magma ocean cumulate pile. Melting of this hybrid source yields liquids with major element abundances and incompatible‐element patterns that are very similar to the Shergotty bulk rock.     

Secondary alteration of the impactite and mineralization in the basal Tertiary sequence,Yaxcopoil‐1, Chicxulub impact crater,Mexico

Abstract The 65 Ma Chicxulub impact crater formed in the shallow coastal marine shelf of the Yucatán Platform in Mexico. Impacts into water‐rich environments provide heat and geological structures that generate and focus sub‐seafloor convective hydrothermal systems. Core from the Yaxcopoil‐1 (Yax‐1) hole, drilled by the Chicxulub Scientific Drilling Project (CSDP), allowed testing for the presence of an impact‐induced hydrothermal system by: a) characterizing the secondary alteration of the 100 m‐thick impactite sequence; and b) testing for a chemical input into the lower Tertiary sediments that would reflect aquagene hydrothermal plume deposition. Interaction of the Yax‐1 impactites with seawater is evident through redeposition of the suevites (unit 1), secondary alteration mineral assemblages, and the subaqueous depositional environment for the lower Tertiary carbonates immediately overlying the impactites. The least‐altered silicate melt composition intersected in Yax‐1 is that of a calc‐alkaline basaltic andesite with 53.4–56 wt% SiO_{2(volatile‐free)}. The primary mineralogy consists of fine microlites of diopside, plagioclase (mainly Ab 47), ternary feldspar (Ab 37 to 77), and trace apatite, titanite, and zircon. The overprinting alteration mineral assemblage is characterized by Mg‐saponite, K‐montmorillonite, celadonite, K‐feldspar, albite, Fe‐oxides, and late Ca and Mg carbonates. Mg and K metasomatism resulted from seawater interaction with the suevitic rocks producing smectite‐K‐feldspar assemblages in the absence of any mixed layer clay minerals, illite, or chlorite. Rare pyrite, sphalerite, galena, and chalcopyrite occur near the base of the impactites. These secondary alteration minerals formed by low temperature (0–150°C) oxidation and fixation of alkalis due to the interaction of glass‐rich suevite with down‐welling seawater in the outer annular trough intersected at Yax‐1. The alteration represents a cold, Mg‐K‐rich seawater recharge zone, possibly recharging higher temperature hydrothermal activity proposed in the central impact basin. Hydrothermal metal input into the Tertiary ocean is shown by elevated Ni, Ag, Au, Bi, and Te concentrations in marcasite and Cd and Ga in sphalerite in the basal 25 m of the Tertiary carbonates in Yax‐1. The lower Tertiary trace element signature reflects hydrothermal metal remobilization from a mafic source rock and is indicative of hydrothermal venting of evolved seawater into the Tertiary ocean from an impact‐generated hydrothermal convective system.     

Composition and heterogeneity of anorthositic impact melt at Mistastin Lake crater, Labrador

Anorthositic impact melt rocks, their target rocks (principally anorthosite, mangerite, granodiorite) and zircon clasts from the ∼36-Ma-old, 28-km-wide Mistastin Lake crater of northern Labrador (55°53′N; 63°18′W) have been examined in order to evaluate the scale and origin of compositional heterogeneities in impact melts produced in craters of moderate size. In particular we assess whether and, if so, how the initial composition of the impact melt was modified as it entrained mineral clasts derived from the underlying rocks over which it flowed when it moved away from the shock-induced, central melting zone. A secondary goal was to determine if zircon clasts in the impact melts are present in the proportions of their target rock sources and/or the substrate lithologies over which they flowed. Chemical compositions of bulk samples of 33 melt rocks and 14 target rocks were measured by XRF and SN-ICPMS. Matrix compositions of nine samples of impact melt rocks were determined by EPMA and LA-ICPMS. Zircon grains from four samples of target rock and zircon clasts from three samples of impact melt rock were measured for multi-element composition, U-Pb age and Hf-isotopic composition by LA-(MC)-ICPMS.The data reveal compositional heterogeneities in the impact melts on the scales of both bulk samples and matrices. Bulk samples can be divided into compositions with high and low concentrations of high-field-strength elements (HFSE; Ti, Zr, Nb) and Fe, Ba, Ce and Y. High HFSE-type melt rocks formed when impact melt entrained large quantities of clasts from mangerite, which is rich in HFSE. Matrix compositions of bulk samples do not show the HFSE distinction but are affected by the introduction of low-temperature melts from the clasts to form dispersed, micron-scale silica-rich heterogeneities.The best estimate of sources of the initial impact melt is ∼73% anorthosite, ∼7% mangerite and ∼20% granodiorite, based on least-squares modeling of major-element compositions of the matrices of thinner flows. Zircon derived from anorthosite can be distinguished from zircon from mangerite and granodiorite by higher Nb/Ta and Eu/Eu* ratios and more negative initial ε Hf values. Zircon clasts >40 mm in size in the impact melt rocks are dominantly or exclusively derived from mangerite and granodiorite rather than from anorthosite. Because anorthosite was the principal source of impact melt at Mistastin, zircon may be a poor provenance indicator for anorthosite contributions to impact melts, particularly where grains smaller than 40 microns are not analyzed.     

Petrogenesis of anomalous Queen Alexandra Range enstatite meteorites and their relation to enstatite chondrites,primitive enstatite achondrites,and aubrites

Queen Alexandra Range (QUE) meteorite 94204 is an anomalous enstatite meteorite whose petrogenesis has been ascribed to either partial melting or impact melting. We studied the meteorite pairs QUE 94204, 97289/97348, 99059/99122/99157/99158/99387, and Yamato (Y)‐793225; these were previously suggested to represent a new grouplet. We present new data for mineral abundances, mineral chemistries, and siderophile trace element compositions (of Fe,Ni metal) in these meteorites. We find that the texture and composition of Y‐793225 are related to EL6, and that this meteorite is unrelated to the QUEs. The mineralogy and siderophile element compositions of the QUEs are consistent with petrogenesis from an enstatite chondrite precursor. We caution that potential re‐equilibration during melting and recrystallization of enstatite chondrite melt‐rocks make it unreliable to use mineral chemistries to assign a specific parent body affinity (i.e., EH or EL). The QUEs have similar mineral chemistries among themselves, while slight variations in texture and modal abundances exist between them. They are dominated by inclusion‐bearing millimeter‐sized enstatite (average En_99.1–99.5) with interstitial spaces filled predominantly by oligoclase feldspar (sometimes zoned), kamacite (Si approximately 2.4 wt%), troilite (≤2.4 wt% Ti), and cristobalite. Siderophile elements that partition compatibly between solid metal and liquid metal are not enriched like in partial melt residues Itqiy and Northwest Africa (NWA) 2526. We find that the modal compositions of the QUEs are broadly unfractionated with respect to enstatite chondrites. We conclude that a petrogenesis by impact melting, not partial melting, is most consistent with our observations.     

Evolution of the winonaite parent body: Clues from silicate mineral trace element distributions

Abstract— We have measured the trace element compositions of individual plagioclase, pyroxene, and olivine grains in 6 different winonaites that span the range of textures and mineralogies observed in these meteorites. Textural evidence in these meteorites, including the presence of a plagioclase/clinopyroxene‐rich lithology and coarse‐grained olivine lithologies, suggests that they may have experienced some silicate partial melting. However, trace element distributions in these lithologies do not show any clear signatures for such an event. Pyroxene trace element compositions do exhibit systematic trends, with abundances generally lowest in Pontlyfni and highest in Winona. The fact that the same trends are present for both incompatible and compatible trace elements suggests, however, that the systematics are more likely the result of equilibration of minerals with initially heterogeneous and distinct compositions, rather than partial melting of a compositionally homogeneous precursor. The winonaites have experienced brecciation and mixing of lithologies, followed by varying degrees of thermal metamorphism on their parent body. These factors probably account for the variable bulk rare earth element (REE) patterns noted for these meteorites and may have led to re‐equilibration of trace elements in different lithologies.     

Major and trace element characteristics of impactites from the Yaxcopoil‐1 borehole,Chicxulub structure,Mexico

Abstract— Approximately 100 m of impactites were retrieved from the ICDP borehole Yaxcopoil‐1 (Yax‐1), located ～60 km south‐southwest from the center of the Chicxulub impact crater on the Yucatán Peninsula of Mexico. Here, we characterize and discuss this impact breccia interval according to its geochemical characteristics. Chemical analysis of samples from all five recognized breccia units reveals that the impactites are of heterogeneous composition with regard to both major and trace elements at the single sample (8–16 cm³) scale. This is primarily due to a strong mixing relationship between carbonate and silicate fractions. However, averaged compositions for suevitic units 1 to 3 are similar, and the silicate fraction (after removal of the carbonate component) indicates thorough mixing and homogenization. Analysis of the green melt breccia horizon, unit 4, indicates that it contains a distinct mafic component. Large brown melt particles (in units 2, 3, and 4) represent a mixture of feldspathic and mafic components, with high CaO abundances. Unit 5 shows the greatest compositional diversity, with highly variable abundances of SiO₂, CaO, and MgO. Inter‐sample heterogeneity is the result of small sample size combined with inherent heterogeneous lithological compositions, highly variable particle size of melt and lithic components, and post‐depositional alteration. In contrast to samples from the Y6 borehole from closer to the center of the structure, Yax‐1 impactites have a strong carbonate component. Elevated loss on ignition, Rb, and Cs contents in the upper two impactite units indicate strong interaction with seawater. The contents of the siderophile elements, including Ni, Co, Ir, and Cr, do not indicate the presence of a significant extraterrestrial component in the Yax‐1 impactites.     

Mineralogy and petrogenesis of lunar magnesian granulitic meteorite Northwest Africa 5744

Lunar meteorite Northwest Africa (NWA) 5744 is a granulitic breccia with an anorthositic troctolite composition that may represent a distinct crustal lithology not previously described. This meteorite is the namesake and first‐discovered stone of its pairing group. Bulk rock major element abundances show the greatest affinity to Mg‐suite rocks, yet trace element abundances are more consistent with those of ferroan anorthosites. The relatively low abundances of incompatible trace elements (including K, P, Th, U, and rare earth elements) in NWA 5744 could indicate derivation from a highlands crustal lithology or mixture of lithologies that are distinct from the Procellarum KREEP terrane on the lunar nearside. Impact‐related thermal and shock metamorphism of NWA 5744 was intense enough to recrystallize mafic minerals in the matrix, but not intense enough to chemically equilibrate the constituent minerals. Thus, we infer that NWA 5744 was likely metamorphosed near the lunar surface, either as a lithic component within an impact melt sheet or from impact‐induced shock.     

Petrography and composition of Martian regolith breccia meteorite Northwest Africa 7475

The Northwest Africa (NWA) 7475 meteorite is one of the several stones of paired regolith breccias from Mars based on petrography, oxygen isotope, mineral compositions, and bulk rock compositions. Its inventory of lithic clasts is dominated by vitrophyre impact melts that were emplaced while they were still molten. Other clast types include crystallized impact melt rocks, evolved plutonic rocks, possible basalts, contact metamorphosed rocks, and siltstones. Impact spherules and vitrophyre shards record airborne transport, and accreted dust rims were sintered on most clasts, presumably during residence in an ejecta plume. The clast assemblage records at least three impact events, one that formed an impact melt sheet on Mars ≤4.4 Ga ago, a second that assembled NWA 7475 from impactites associated with the impact melt sheet at 1.7–1.4 Ga, and a third that launched NWA 7475 from Mars ~5 Ma ago. Mildly shocked pyroxene and plagioclase constrain shock metamorphic conditions during launch to >5 and <15 GPa. The mild postshock‐heating that resulted from these shock pressures would have been insufficient to sterilize this water‐bearing lithology during launch. Magnetite, maghemite, and pyrite are likely products of secondary alteration on Mars. Textural relationships suggest that calcium‐carbonate and goethite are probably of terrestrial origin, yet trace element chemistry indicates relatively low terrestrial alteration. Comparison of Mars Odyssey gamma‐ray spectrometer data with the Fe and Th abundances of NWA 7475 points to a provenance in the ancient southern highlands of Mars. Gratteri crater, with an age of ~5 Ma and an apparent diameter of 6.9 km, marks one possible launch site of NWA 7475.     

Martian meteorite Dhofar 019: A new shergottite

Abstract— Dhofar 019 is a new martian meteorite found in the desert of Oman. In texture, mineralogy, and major and trace element chemistry, this meteorite is classified as a basaltic shergottite. Olivine megacrysts are set within a groundmass composed of finer grained olivine, pyroxene (pigeonite and augite), and maskelynite. Minor phases are chromite‐ulvöspinel, ilmenite, silica, K‐rich feldspar, merrillite, chlorapatite, and pyrrhotite. Secondary phases of terrestrial origin include calcite, gypsum, celestite, Fe hydroxides, and smectite. Dhofar 019 is most similar to the Elephant Moraine (EETA) 79001 lithology A and Dar al Gani (DaG) 476/489 shergottites. The main features that distinguish Dhofar 019 from other shergottites are lack of orthopyroxene; lower Ni contents of olivine; the heaviest oxygen‐isotopic bulk composition; and larger compositional ranges for olivine, maskelynite, and spinel, as well as a wide range for pyroxenes. The large compositional ranges of the minerals are indicative of relatively rapid crystallization. Modeling of olivine chemical zonations yield minimum cooling rates of 0.5‐0.8 °C/h. Spinel chemistry suggests that crystallization took place under one of the most reduced conditions for martian meteorites, at an fO₂ 3 log units below the quartz‐fayalite‐magnetite (QFM) buffer. The olivine megacrysts are heterogeneously distributed in the rock. Crystal size distribution analysis suggests that they constitute a population formed under steady‐state conditions of nucleation and growth, although a few grains may be cumulates. The parent melt is thought to have been derived from partial melting of a light rare earth element‐ and platinum group element‐depleted mantle source. Shergottites, EETA79001 lithology A, DaG 476/489, and Dhofar 019, although of different ages, comprise a particular type of martian rocks. Such rocks could have formed from chemically similar source(s) and parent melt(s), with their bulk compositions affected by olivine accumulation.     

Accessory and opaque minerals in impact melt rocks of the Boltysh structure,Ukraine

Electron microprobe analyses of accessory and opaque minerals from the impact melt rocks of the Boltysh structure, in the central part of the Ukrainian Shield, are presented in this report. Our study establishes a variety of minerals represented by native metals, alloys, oxides, sulfides, phosphates, and silicates, formed during several stages of cooling and solidification of the thick impact melt sheet. Baddeleyite was determined to be the earliest high‐temperature mineral to occur in the impact melt rocks. Iron and titanium oxides crystallized earlier or simultaneously with the microliths of orthopyroxene and feldspars. High concentrations of TiO₂, Al₂O₃, and Cr₂O₃ were identified in some hematite varieties. Cu‐ and Ni‐bearing pyrrhotites occur in impact melt rocks with a glassy matrix. Native metals—copper, platinum, and silver—were likely formed due to the hydrothermal alteration of the upper unit of the impact melt sheet. Zircon is the only accessory mineral found in impact melt rocks that is preserved from the basement granites of the Boltysh structure.     

Ni/S/Cl systematics and the origin of impact‐melt glasses in Martian meteorite Elephant Moraine 79001

Martian meteorite Elephant Moraine A79001 (EET 79001) has received considerable attention for the unusual composition of its shock melt glass, particularly its enrichment in sulfur relative to the host shergottite. It has been hypothesized that Martian regolith was incorporated into the melt or, conversely, that the S‐enrichment stems from preferential melting of sulfide minerals in the host rock during shock. We present results from an electron microprobe study of EET 79001 including robust measurements of major and trace elements in the shock melt glass (S, Cl, Ni, Co, V, and Sc) and minerals in the host rock (Ni, Co, and V). We find that both S and major element abundances can be reconciled with previous hypotheses of regolith incorporation and/or excess sulfide melt. However, trace element characteristics of the shock melt glass, particularly Ni and Cl abundances relative to S, cannot be explained either by the incorporation of regolith or sulfide minerals. We therefore propose an alternative hypothesis whereby, prior to shock melting, portions of EET 79001 experienced acid‐sulfate leaching of the mesostasis, possibly groundmass feldspar, and olivine, producing Al‐sulfates that were later incorporated into the shock melt, which then quenched to glass. Such activity in the Martian near‐surface is supported by observations from the Mars Exploration Rovers and laboratory experiments. Our preimpact alteration model, accompanied by the preferential survival of olivine and excess melting of feldspar during impact, explains the measured trace element abundances better than either the regolith incorporation or excess sulfide melting hypothesis does.     

Petrology and trace element geochemistry of Tissint,the newest shergottite fall

The fall and recovery of the Tissint meteorite in 2011 created a rare opportunity to examine a Martian sample with a known, short residence time on Earth. Tissint is an olivine‐phyric shergottite that accumulated olivine antecrysts within a single magmatic system. Coarse olivine grains with nearly homogeneous cores of Mg# >80 suggest slow re‐equilibration. Many macroscopic features of this sample resemble those of LAR 06319, including the olivine crystal size distribution and the presence of evolved oxide and olivine compositions. Unlike LAR 06319, however, no magmatic hydrous phases were found in the analyzed samples of Tissint. Minor and trace element compositions indicate that the meteorite is the product of closed‐system crystallization from a parent melt derived from a depleted source, with no obvious addition of a LREE‐rich (crustal?) component prior to or during crystallization. The whole‐rock REE pattern is similar to that of intermediate olivine‐phyric shergottite EETA 79001 lithology A, and could also be approximated by a more olivine‐rich version of depleted basaltic shergottite QUE 94201. Magmatic oxygen fugacities are at the low end of the shergottite range, with log fO₂ of QFM‐3.5 to ‐4.0 estimated based on early‐crystallized minerals and QFM‐2.4 estimated based on the Eu in pyroxene oxybarometer. These values are similarly comparable to other depleted shergottites, including SaU 005 and QUE 94201. Tissint occupies a previously unsampled niche in shergottite chemistry: containing olivines with Mg# >80, resembling the enriched olivine‐phyric shergottite LAR 06319 in its crystallization path, and comparable to intermediate olivine‐phyric shergottite EETA 79001A, depleted olivine‐phyric shergottite DaG 476, and depleted basaltic shergottite QUE 94201 in its trace element abundances and oxygen fugacity. The apparent absence of evidence for terrestrial alteration in Tissint (particularly in trace element abundances in the whole‐rock and individual minerals) confirms that exposure to the arid desert environment results in only minimal weathering of samples, provided the exposure times are brief.