Shock‐induced melting,recrystallization, and exsolution in plagioclase from the Martian lherzolitic shergottite GRV 99027

Abstract— Plagioclase in the Martian lherzolitic shergottite Grove Mountains (GRV) 99027 was shocked, melted, and recrystallized. The recrystallized plagioclase contains lamellae of pyroxene, olivine, and minor ilmenite (<1 μm wide). Both the pyroxene and the olivine inclusions enclosed in plagioclase and grains neighboring the plagioclase were partially melted into plagioclase melt pools. The formation of these lamellar inclusions in plagioclase is attributed to exsolution from recrystallizing melt. Distinct from other Martian meteorites, GRV 99027 contains no maskelynite but does contain recrystallized plagioclase. This shows that the meteorite experienced a slower cooling than maskelynite‐bearing meteorites. We suggest that the parent rock of GRV 99027 could have been embedded in hot rocks, which facilitated a more protracted cooling history.     

Rb‐Sr and Sm‐Nd isotopic and REE studies of igneous components in the bulk matrix domain of Martian breccia Northwest Africa 7034

The bulk matrix domain of the Martian breccia NWA 7034 was examined petrographically and isotopically to better understand the provenance and age of the source material that make up the breccia. Both ¹⁴⁷Sm‐¹⁴³Nd and ¹⁴⁶Sm‐¹⁴²Nd age results for mineral separates from the bulk matrix portion of breccia NWA 7034 suggest that various lithological components in the breccia probably formed contemporaneously ~4.44 Ga ago. This old age is in excellent agreement with the upper intersection ages (4.35–4.45 Ga) for U‐Pb discordia and also concordia defined by zircon and baddeleyite grains in matrix and igneous‐textured clasts. Consequently, we confirm an ancient age for the igneous components that make up the NWA 7034 breccia. Substantial disturbance in the Rb‐Sr system was detected, and no age significance could be gleaned from our Rb‐Sr data. The disturbance to the Rb‐Sr system may be due to a thermal event recorded by bulk‐rock K‐Ar ages of 1.56 Ga and U‐Pb ages of phosphates at about 1.35–1.5 Ga, which suggest partial resetting from an unknown thermal event(s), possibly accompanying breccia formation. The NWA 7034 bulk rock is LREE enriched and similar to KREEP‐rich lunar rocks, which indicates that the earliest Martian crust was geochemically enriched. This enrichment supports the idea that the crust is one of the enriched geochemical reservoirs on Mars that have been detected in studies of other Martian meteorites.     

Bulk chemical composition of lherzolitic shergottite Grove Mountains 99027—Constraints on the mantle of Mars

Abstract— We report the concentration of 50 elements, including rare earth elements (REEs) and platinum group elements (PGEs) in bulk samples of the Grove Mountains (GRV) 99027 lherzolitic shergottite. The abundances of REEs are distinctly lower than those of Allan Hills (ALH) A77005 and other lherzolitic shergottites, indicating that GRV 99027 is not paired with them. It may, nevertheless, sample the same igneous unit as the others (Lin et al. 2005b; Wang and Chen 2006). The CI‐normalized elemental pattern of GRV 99027 reveals low (0.004–0.008 × CI) and unfractionated PGEs (except for Pd of 0.018 × CI) without depletion of W. or Ga relative to lithophile element trends. Fractionation between siderophile and lithophile elements become less pronounced with increase of volatility, except for high abundances of Ni and Co. These characteristics are probably representative of the mantle of Mars, which is consistent with previous work that the Martian mantle formed in a deep magma ocean followed by a later accretion of chondritic materials.     

147Sm‐143Nd and 176Lu‐176Hf systematics of eucrite and angrite meteorites

Comparative planetary geochemistry provides insight into the origin and evolutionary paths of planetary bodies in the inner solar system. The eucrite and angrite achondrite groups are particularly interesting because they show evidence of early planetary differentiation. We present ¹⁴⁷Sm‐¹⁴³Nd and ¹⁷⁶Lu‐¹⁷⁶Hf analyses of eight noncumulate (basaltic) eucrites, two cumulate eucrites, and three angrites, which together place new constraints on the evolution and differentiation histories of the crusts of the eucrite and angrite parent bodies and their mantle mineralogies. The chemical compositions of both eucrites and angrites indicate similar evolutionary paths and petrogenetic models with formation and isolation of differentiated crustal reservoirs associated with segregation of ilmenite. We report a ¹⁴⁷Sm‐¹⁴³Nd mineral isochron age for the Moama cumulate eucrite of 4519 ± 34 Ma (MSWD = 1.3). This age indicates protracted magmatism within deep crustal layers of the eucrite parent body lasting up to about 50 Ma after the formation of the solar system. We further demonstrate that the isotopic compositions of constituent minerals are compromised by secondary processes hindering precise determination of mineral isochron ages of basaltic eucrites and angrites. We interpret the changes in geochemistry and, consequently, the erroneous ¹⁴⁷Sm‐¹⁴³Nd and ¹⁷⁶Lu‐¹⁷⁶Hf internal mineral isochron ages of basaltic eucrites and angrites as the result of metamorphic events such as impacts (effects from pressure, temperature, and peak shock duration) on the surfaces of the eucrite and angrite parent bodies.     

Petrogenesis of the new lherzolitic shergottite Grove Mountains 99027: Constraints of petrography,mineral chemistry,and rare earth elements

Abstract— We report petrography, mineral chemistry, and microdistribution of rare earth elements (REE) in a new lherzolitic shergottite, Grove Mountains (GRV) 99027. The textural relationship and REE patterns of minerals suggest precipitation of cumulus olivine and chromite, followed by equilibrium crystallization of a closed system with a bulk composition of the inferred intercumulus melt. Subsolidus equilibrium temperatures of pyroxenes and olivine range from 1100 to 1210 °C, based on a two‐pyroxene thermometry and Ca partitioning between augite and olivine. Oxygen fugacity of the parent magma is 1.5–2.5 (av. 2.0 ± 0.4) log units below the quartz‐fayalite‐magnetite (QFM) buffer at 960–1360 °C, according to the olivine‐orthopyroxene‐chromite barometer. The ilmenite‐chromite barometer and thermometer show much wider ranges of oxygen fugacity (1.0–7.0 log unit below QFM) and temperature (1130–480 °C), suggesting subsolidus equilibration of the oxides at low temperatures, probably due to deep burial of GRV 99027 on Mars. The low oxygen fugacity and LREE depletion of the parent magma of GRV 99027 suggest low contamination by martian crust. Characteristics of GRV 99027 demonstrate similarity of lherzolitic shergottites, suggesting a high possibility of launch pairing or a homogeneous upper mantle of Mars if they were ejected by individual impact events. However, GRV 99027 probably experienced severe post‐shock thermal metamorphism in comparison with other lherzolitic shergottites, based on the re‐crystallization of maskelynite, the homogeneity of minerals, and the low subsolidus equilibrium temperatures between chromite and ilmenite.     

Defining the mechanisms that disturb the Sm‐Nd isotopic systematics of the Martian meteorites: Examples from Dar al Gani 476 and Allan Hills 77005

Abstract— Microbeam studies of Martian meteorites Dar al Gani (DaG) 476 and Allan Hills (ALH) 77005 have been conducted to identify potential causes of disequilibrium exhibited in their Sm‐Nd isotopic systematics. Olivine and maskelynite mineral fractions on the DaG 476 isochron are displaced relative to their positions as dictated by measured mineral compositions. The olivine mineral fractions from ALH 77005 not only have a relatively low Sm/Nd ratio, but appear to contain an unradiogenic component that shifts the olivine mineral fraction off the isochron defined by the pyroxene and maskelynite mineral fractions. Trace components such as melt inclusions, impact melt, high‐Si mesostasis, and altered olivine were analyzed using scanning electron microscopy, quantitative electron microscopy, and secondary ion mass spectrometry to determine their potential for disturbing the isotopic systematics of the mineral fractions, assuming that the mineral fractions were not completely pure. Mixing models indicate that the presence of melt inclusions in the DaG 476 olivine mineral fraction lowered its Sm/Nd ratio. The maskelynite mineral fraction contains a related but more evolved mesostasis component that raised the Sm/Nd ratio of the fraction. The position of two olivine mineral fractions below the ALH 77005 isochron is interpreted to reflect small additions of impact melt with a light rare earth element enriched pattern and a non‐indigenous, unradiogenic Nd component. Furthermore, the presence of rare earth elements in olivine and maskelynite from both igneous and non‐igneous components such as melt inclusions, mesostasis, and impact melt is observed on a fine (<30 μm) scale. Despite the addition of this material, the Sm‐Nd ages are not affected. This study demonstrates that detailed mineral separation procedures as employed by modern geochronology laboratories permit reliable ages to be derived from shocked and altered samples.     

Grove Mountains 020090 enriched lherzolitic shergottite: A two‐stage formation model

Grove Mountains (GRV) 020090 is an enriched lherzolitic shergottite, distinct from other lherzolitic shergottites, except RBT 04262/1. Its characteristics include high abundance of plagioclase (24.2 vol% in the nonpoikilitic area), presence of K‐feldspar, common occurrence of baddeleyite, high FeO contents of olivine (bimodal peaks at Fa 33 mol% and Fa 41 mol%) and low‐Ca pyroxenes (bimodal peaks at Fs 23.8–31.7 mol% and Fs 25.7–33.9 mol%), and significant LREE enrichment of phosphates (500–610 × CI). The bulk composition of GRV 020090 suggests derivation from partial melting of an enriched reservoir. However, the REE patterns of the cores of pigeonite oikocrysts and the olivine chadacrysts are indistinguishable from those of GRV 99027 and other moderately depleted lherzolitic shergottites, and reveal a LREE‐depleted pattern of the primordial parent magma. We propose that the primordial parent magma of GRV 020090 was derived from a moderately depleted Martian upper mantle reservoir, and later the residual melt was contaminated by oxidized and enriched Martian crustal materials as it ascended up to the subsurface. GRV 020090 and RBT 04262/1 may have sampled an igneous unit different from other lherzolitic shergottites.     

High‐pressure polymorphs of magnesian orthopyroxene from a shock vein in the Yamato‐000047 lherzolitic shergottite

Abstract– We found a simple thin shock vein, less than or equal to about 60 μm in width and 1.8 mm in length, in the poikilitic area in the Yamato (Y‐) 000047 lherzolitic shergottite. The shock vein occurs only in magnesian Ca‐poor clinopyroxene, which may have transformed from orthopyroxene during the pressure increase at the shock event. The shock vein consists of (Mg_0.8,Fe_0.2)SiO₃ pyroxene polymorphs, such as columnar akimotoite, two kinds of pyroxene glasses, dendritic akimotoite, and framboidal pyroxene glass, in the order from the periphery to the center. The compositions and textures suggest that columnar akimotoite in the periphery of the shock vein crystallized from solid‐state phase transition of clinopyoroxene during the cooling of the vein, and the remains in the shock vein solidified from shock‐produced melt. The glass includes two kinds of massive glass in the vein and framboidal glass in the vein center. The framboidal glass is the most magnesian and may have been vitrified from perovskite crystallized from high‐pressure melt produced at high temperature ≥3000 °C and high‐pressure 23–40 GPa. Dendritic akimotoites in the vein center metastably crystallized from residual shock melt. The formation sequences of the constituent phases in the shock vein happen in the following order: columnar akimotoites, rim glass, center glass, framboidal glass, and dendritic akimotoites. The increase of the Raman intensity of 660–670 cm^?1 in the order of rim glass, center glass, and framboidal glass suggests that the formation of the pyroxene chain proceeds faster in the vein center than in the vein rim due to its slower cooling. The finding of the shock vein consisting merely of high‐pressure polymorphs of pyroxene, akimotoite, and framboidal glass (vitrified perovskite) is the first reported among all Martian meteorites.     

Two‐stage polybaric formation of the new enriched,pyroxene‐oikocrystic,lherzolitic shergottite,NWA 7397

Northwest Africa (NWA) 7397 is a newly discovered, enriched, lherzolitic shergottite, the third described example of this group. This meteorite consists of two distinct textural lithologies (1) poikilitic—comprised of zoned pyroxene oikocrysts, with chadacrysts of chromite and olivine, and (2) nonpoikilitic—comprised of olivine, low‐Ca and high‐Ca pyroxene, maskelynite, and minor abundances of merrillite, spinel, ilmenite, and pyrrhotite. The constant Ti/Al ratios of pyroxene oikocrysts suggests initial crystallization of the poikilitic lithology at depth (equivalent to pressures of approximately 10 kbar), followed by crystallization of the nonpoikilitic lithology at shallower levels. Oxygen fugacity conditions become more oxidizing during crystallization ranging from fO₂ conditions of approximately QFM‐2 to QFM‐0.7. Magma calculated to be in equilibrium with the major rock‐forming minerals is LREE‐enriched relative to depleted or intermediate shergottites and has flat overall profiles. Therefore, we suggest that the parental magma for NWA 7397 had sampled an enriched, oxidized, Martian geochemical source, similar to that of other enriched basaltic and olivine‐phyric shergottites. We present a polybaric formation model for the lherzolitic shergottite NWA 7397, to account for the petrologic constraints. Three successive stages in the development of NWA 7397 are discussed (1) formation of a REE‐enriched parental magma from a distinct Martian mantle reservoir; (2) magma ponding and development of a staging chamber concomitant with initial crystallization of the poikilitic lithology; and (3) magma ascent to the near surface, with entrainment of cumulates from the staging chamber and subsequent crystallization of the nonpoikilitic lithology en route to the surface.     

Petrogenesis and shock metamorphism of the enriched lherzolitic shergottite Northwest Africa 7755

Northwest Africa (NWA) 7755 is a newly found enriched lherzolitic shergottite. Here, we report its detailed petrography and mineralogy. NWA 7755 contains both poikilitic and non‐poikilitic lithologies. Olivine has different compositional ranges in the poikilitic and non‐poikilitic lithologies, Fa_30–39 and Fa_37–40, respectively. Pyroxene in the non‐poikilitic lithology is systematically Fe‐richer than that in the poikilitic lithology. The chromite grains in non‐poikilitic lithology are highly Ti‐richer than those in the poikilitic lithology. The chemical variations of olivine, pyroxene, and chromite between the poikilitic and non‐poikilitic lithologies support a two‐stage formation model of lherzolitic shergottites. Besides planar fractures and strong mosaicism in olivine and pyroxene, shock‐induced melt veins and pockets are observed in NWA 7755. Olivine grains within and adjacent to melt veins and/or pockets have either transformed to ringwoodite, amorphous phase, or dissociated to bridgmanite plus magnesiowüstite. Merrillite in melt veins has completely transformed to tuite; however, apatite only has partially transformed to tuite, indicating a relatively sluggish transformation rate. The partial transformation from apatite to tuite resulted in fractional devolatilization of Cl and F in apatite. The fine‐grained mineral assemblage in melt veins consists mainly of bridgmanite, minor magnesiowüstite, Fe‐sulfide, Fe‐phosphide, and Ca‐phosphate minerals. The coexistence of bridgmanite and magnesiowüstite in these veins indicates a shock pressure of >~24 GPa and a temperature of 1800–2000 °C. Coesite and seifertite are probably present in NWA 7755. The presence of these high‐pressure minerals indicates that NWA 7755 has experienced a more intense shock metamorphism than other enriched lherzolitic shergottites.     

Geochemistry and Sm‐Nd chronology of a Stannern‐group eucrite,Northwest Africa 7188

We report the results of a detailed study of the basaltic eucrite Northwest Africa (NWA) 7188, including its mineralogical and bulk geochemical characteristics, oxygen isotopic composition, and ^147,146Sm‐^143,142Nd mineral isochron ages. The texture and chemical composition of pyroxene and plagioclase demonstrate that NWA 7188 is a monomict eucrite with a metamorphic grade of type 4. The oxygen isotopic composition and the Fe/Mn ratios of pyroxene confirmed that NWA 7188 belongs to the howardite–eucrite–diogenite meteorite suite, generally considered to originate from asteroid 4 Vesta. Whole‐rock TiO₂, La, and Hf concentrations and a CI chondrite‐normalized rare earth element pattern are in good agreement with those of representative Stannern‐group eucrites. The ^147,146Sm‐^143,142Nd isochrons for NWA 7188 yielded ages of 4582 ± 190 and 4554 +17/?19 Ma, respectively. The closure temperature of the Sm‐Nd system for different fractions of NWA 7188 was estimated to be >865 °C, suggesting that the Sm‐Nd decay system has either been resistant to reheating at ~800 °C during the global metamorphism or only partially reset. Therefore, the ¹⁴⁶Sm‐¹⁴²Nd age of NWA 7188 corresponds to the period of initial crystallization of basaltic magmas and/or global metamorphism on the parent body, and is unlikely to reflect Sm‐Nd disturbance by late reheating and impact events. In either case, NWA 7188 is a rare Stannern‐group eucrite that preserves the chronological information regarding the initial crustal evolution of Vesta.     

Petrology of magmatic silicate inclusions in the Allan Hills 77005 lherzolitic shergottite

Abstract— Magmatic inclusions occur in both chadacrystic olivine and oikocrystic pigeonite in ALH 77005 but are different from each other. Magmatic inclusions in olivine consist mainly of aluminous pyroxenes, intergrowths of plagioclase and silica, silica-predominant glass, and rhyodacitic glass, with minor amounts of chromite, spinel, pyrrhotite, and whitlockite. Those in pigeonite consist mainly of aluminous pyroxenes, nonaluminous ferroan pyroxenes, kaersutite, spinel, and K-rich trachytic glass, with minor amounts of pyrrhotite and whitlockite. The magmatic inclusions in chadacrystic olivine formed from trapped melts that were basaltic, apparently dry and crystallized additional olivine metastably. The basaltic magma, with entrained olivine, experienced magma mixing with K-rich and wet magmas, or assimilation of such crustal rocks, in the early to middle stages of the crystallization sequence of ALH 77005 during crystallization of chadacrystic olivine prior to precipitation of oikocrystic pigeonite. However the amount of mixed magmas or assimilated rocks was minor in comparison to the basaltic magma. Crystallization of pigeonite, augite, and plagioclase in the host lithologies took place in a shallow magma reservoir under an open-system condition, and the pigeonite trapped basaltic andesite to trachyandesitic melts, which resulted in magmatic inclusions in oikocrystic pigeonite. The magmatic inclusions in both olivine and pigeonite were formed under a rapid-cooling condition, resulting in a variety of inclusions. Kaersutite in magmatic inclusions in oikocrystic pigeonite crystallized under a closed-system wet condition during the late-stage crystallization of the inclusions.     

The noble gas concentrations of the Martian meteorites GRV 99027 and paired NWA 7906/NWA 7907

Here we present the isotopic concentrations of He, Ne, Ar, Kr, and Xe for the three Martian meteorites, namely Grove Mountains 99027 (GRV 99027), Northwest Africa 7906 (NWA 7906), and Northwest Africa 7907 (NWA 7907). The cosmic ray exposure (CRE) age for GRV 99027 of 5.7 ± 0.4 Ma (1σ) is consistent with CRE ages for other poikilitic basaltic shergottites and suggests that all were ejected in a single event ~5.6 Ma ago. After correcting for an estimated variable sodium concentration, the CRE ages for NWA 7906 and NWA 7907 of 5.4 ± 0.4 and 4.9 ± 0.4 Ma (1σ), respectively, are in good agreement with the CRE age of ~5 Ma favored by Cartwright et al. ( 2014 ) for NWA 7034. The data, therefore, support the conclusion that all three basaltic regolith breccias are paired. The ⁴⁰Ar gas retention age for NWA 7907 of ~1.3 Ga is in accord with Cartwright et al. ( 2014 ). For NWA 7906, we were unable to determine a ⁴⁰Ar gas retention age. The ⁴He gas retention ages for NWA 7906 and 7907 are in the range of 200 Ma and are much shorter than the ⁴⁰Ar gas retention age of NWA 7907, indicating that about 86–88% of the radiogenic ⁴He has been lost. The Kr and Xe isotopic concentrations in GRV 99027 are composed almost exclusively of Martian interior (MI) gases, while for NWA 7906 and NWA 7907, they indicate gases from the MI, elementally fractionated air, and possibly Martian atmosphere.     

Geochemistry of intermediate olivine‐phyric shergottite Northwest Africa 6234, with similarities to basaltic shergottite Northwest Africa 480 and olivine‐phyric shergottite Northwest Africa 2990

Abstract— The newly found meteorite Northwest Africa 6234 (NWA 6234) is an olivine (ol)‐phyric shergottite that is thought, based on texture and mineralogy, to be paired with Martian shergottite meteorites NWA 2990, 5960, and 6710. We report bulk‐rock major‐ and trace‐element abundances (including Li), abundances of highly siderophile elements, Re‐Os isotope systematics, oxygen isotope ratios, and the lithium isotope ratio for NWA 6234. NWA 6234 is classified as a Martian shergottite, based on its oxygen isotope ratios, bulk composition, and bulk element abundance ratios, Fe/Mn, Al/Ti, and Na/Al. The Li concentration and δ⁷Li value of NWA 6234 are similar to that of basaltic shergottites Zagami and Shergotty. The rare earth element (REE) pattern for NWA 6234 shows a depletion in the light REE (La‐Nd) compared with the heavy REE (Sm‐Lu), but not as extreme as the known “depleted” shergottites. Thus, NWA 6234 is suggested to belong to a new category of shergottite that is geochemically “intermediate” in incompatible elements. The only other basaltic or ol‐phyric shergottite with a similar “intermediate” character is the basaltic shergottite NWA 480. Rhenium‐osmium isotope systematics are consistent with this intermediate character, assuming a crystallization age of 180 Ma. We conclude that NWA 6234 represents an intermediate compositional group between enriched and depleted shergottites and offers new insights into the nature of mantle differentiation and mixing among mantle reservoirs in Mars.     

Spinels and oxygen fugacity in olivine‐phyric and lherzolitic shergottites

Abstract— We examine the occurrences, textures, and compositional patterns of spinels in the olivine‐phyric shergottites Sayh al Uhaymir (SaU) 005, lithology A of Elephant Moraine A79001 (EET‐A), Dhofar 019, and Northwest Africa (NWA) 1110, as well as the Iherzolitic shergottite Allan Hills (ALH) A77005, in order to identify spinel‐olivine‐pyroxene assemblages for the determination of oxygen fugacity (using the oxybarometer of Wood [1991]) at several stages of crystallization. In all of these basaltic martian rocks, chromite was the earliest phase and crystallized along a trend of strict Cr‐Al variation. Spinel (chromite) crystallization was terminated by the appearance of pyroxene but resumed later with the appearance of ulvöspinel. Ulvöspinel formed overgrowths on early chromites (except those shielded as inclusions in olivine or pyroxene), retaining the evidence of the spinel stability gap in the form of a sharp core/rim boundary (except in ALH A77005, where subsolidus reequilibration diffused this boundary). Secondary effects seen in chromites include reaction with melt before ulvöspinel overgrowth, reaction with melt inclusions, reaction with olivine hosts (in ALH A77005), and exsolution of ulvöspinel or ilmenite. All chromites experienced subsolidus Fe/Mg reequilibration. Spinel‐olivine‐pyroxene assemblages representing the earliest stages of crystallization in each rock essentially consist of the highest‐Cr#, lowest‐fe# chromites not showing secondary effects plus the most magnesian olivine and equilibrium low‐Ca pyroxene. Assemblages representing the onset of ulvöspinel crystallization consist of the lowest‐Ti ulvöspinel, the most magnesian olivine in which ulvöspinel occurs as inclusions, and equilibrium low‐Ca pyroxene. The results show that, for early crystallization conditions, oxygen fugacity (fO₂) increases from SaU 005 and Dhofar 019 (?QFM ‐3.8), to EET‐A (QFM ‐2.8) and ALH A77005 (QFM ‐2.6), to NWA 1110 (QFM ‐1.7). Estimates for later conditions indicate that in SaU 005 and Dhofar 019 oxidation state did not change during crystallization. In EET‐A, there was an increase in fO₂ that may have been due to mixing of reduced material with a more oxidized magma. In NWA 1110, there was a dramatic increase, indicating a non‐buffered system, possibly related to its high oxidation state. Differences in fO₂ among shergottites are not primarily due to igneous fractionation but, rather, to derivation from (and possibly mixing of) different reservoirs.     

Evidence from the Rb‐Sr system for 4.4 Ga alteration of chondrules in the Allende (CV3) parent body

Abstract— The timing and processes of alteration in the CV parent body are investigated by the analysis of Sr isotopes, major and trace elements, and petrographic type and distribution of the secondary minerals (nepheline and sodalite) in 22 chondrules from the Allende (CV3) chondrite. The Sr isotopic compositions of the chondrules are scattered around the 4.0 Ga reference line on the ⁸⁷Sr/⁸⁶Sr evolution diagram, indicating that the chondrules have been affected by late thermal alteration event(s) in the parent body. The degree of alteration, determined for individual chondrules based on the distribution of nepheline and sodalite, is unrelated to the disturbance of the Rb‐Sr system, suggesting that the alteration process that produced nepheline and sodalite is different from the thermal process that disturbed the Rb‐Sr system of the chondrules. Considering the geochemical behavior of Rb and Sr, the main host phase of Sr in chondrules is likely to be mesostasis, which could be most susceptible to late thermal alteration. As there is a poor connection between the alteration degree determined from abundances of nepheline and sodalite and the disturbance of Rb‐Sr isotopic system, we consider the mesostasis to provide a constraint on the late parent body alteration process. From this point of view, 23 mesostasis‐rich chondrules, including those from literature data, were selected. The selected chondrules are closely correlated on the ⁸⁷Sr/⁸⁶Sr evolution diagram, with an inferred age of 4.36 ± 0.08 Ga. This correlation would represent an age of the final major Sr isotopic redistribution of the chondrules in the parent body.     

Nd and Sr isotopic evidence for the origin of tektite material from DSDP site 612 off the New Jersey coast

Abstract— Late Eocene tektite material from DSDP site 612 is composed of angular to spherical tektites and microtektites containing abundant vesicles and a few unmelted to partially melted mineral inclusions. The major element compositions of the 612-tektites are generally comparable to those of North American tektites, but the physical features suggest that the DSDP-612 tektites were formed by less severe shock melting. The ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd compositions of 612-tektites: a) show much wider ranges than the tightly constrained group of North American tektites and microtektites, and b) are significantly different from those of other groups of tektites. The existence of large isotopic variations in tektites from DSDP site 612 requires that they were formed from a chemically and isotopically heterogeneous material in a regime that is distinctive from that of other groups of tektites. T^ND_CHUR and T^Sr_UR model ages of the 612-tektites indicate that they were formed from a crustal source of late Precambrian mean age (800–1000 Ma) which in middle Palaeozoic time (?400 Ma) was further enriched in Rb/Sr during sedimentary processes. These source characteristics suggest that the impact which produced the 612-tektites occurred in rocks of the Appalachian orogeny or sediments derived from this orogenic belt. Potential source materials for both 612-tektites and North American tektites are present on the eastern and southeastern part of the North American continent and its adjacent shelf. The distinct isotopic differences between 612-tektites and North American tektites indicate that the two groups of tektites were either formed by the impact of more than one bolide in the same general area, or by a single impact event that sampled different layers.     

Mn‐Cr isotope systematics of the D'Orbigny angrite

Abstract— We have conducted a detailed study of the Mn‐Cr systematics of the angrite D'Orbigny. Here, we report Cr isotopic abundances and Mn/Cr ratios in olivine, pyroxene, glass, chromite, and bulk rock samples from D'Orbigny. ⁵³Cr excesses in these samples correlate well with their respective Mn/Cr ratios and define an isochron with a slope that corresponds to an initial ⁵³Mn/⁵⁵Mn ratio = (3.24 ± 0.04) × 10^?6 and initial ⁵³Cr/⁵²Cr ratio of ?(53) = 0.30 ± 0.03 at the time of isotopic closure. The ⁵³Mn/⁵⁵Mn ratio of the D'Orbigny bulk rock is more than two‐fold the ⁵³Mn/⁵⁵Mn ratio of the angrites Lewis Cliff 86010 (LEW) and Angra dos Reis (ADOR) and implies an older Mn‐Cr age of 4562.9 ± 0.6 Ma for D'Orbigny relative to a Pb‐Pb age of 4557.8 ± 0.5 Ma for LEW and ADOR. One of the most unusual aspects of D'Orbigny is the presence of glass, a phase that has not been identified in any of the other angrites. The Mn‐Cr data for glass and a pyroxene fraction found in druses indicate that they formed contemporaneously with the main phases of the meteorite. Since the Mn‐Cr age of D'Orbigny is ?5 Ma years older than the angrites LEW and ADOR, D'Orbigny likely represents an earlier stage in the evolution of the angrite parent body.     

Target rocks,impact glasses,and melt rocks from the Lonar crater,India: Highly siderophile element systematics and Sr‐Nd‐Os isotopic signatures

The Lonar crater is a ~0.57‐Myr‐old impact structure located in the Deccan Traps of the Indian peninsula. It probably represents the best‐preserved impact structure hosted in continental flood basalts, providing unique opportunities to study processes of impact cratering in basaltic targets. Here we present highly siderophile element (HSE) abundances and Sr‐Nd and Os isotope data for target basalts and impactites (impact glasses and impact melt rocks) from the Lonar area. These tools may enable us to better constrain the interplay of a variety of impact‐related processes such as mixing, volatilization, and contamination. Strontium and Nd isotopic compositions of impactites confirm and extend earlier suggestions about the incorporation of ancient basement rocks in Lonar impactites. In the Re‐Os isochron plot, target basalts exhibit considerable scatter around a 65.6 Myr Re‐Os reference isochron, most likely reflecting weathering and/or magma replenishment processes. Most impactites plot at distinctly lower ¹⁸⁷Re/¹⁸⁸Os and ¹⁸⁷Os/¹⁸⁸Os ratios compared to the target rocks and exhibit up to two orders of magnitude higher abundances of Ir, Os, and Ru. Moreover, the impactites show near‐chondritic interelement ratios of HSE. We interpret our results in terms of an addition of up to 0.03% of a chondritc component to most impact glasses and impact melt rocks. The magnitude of the admixture is significantly lower than the earlier reported 12–20 wt% of extraterrestrial component for Lonar impact spherules, reflecting the typical difference in the distribution of projectile component between impact glass spherules and bulk impactites.     

Chromium isotopic systematics of the Sutter's Mill carbonaceous chondrite: Implications for isotopic heterogeneities of the early solar system

Recent studies have shown that major meteorite groups possess their own characteristic ⁵⁴Cr values, demonstrating the utility of Cr isotopes for identifying genetic relationships between the planetary materials in conjunction with other classical tools, such as oxygen isotopes. In this study, we performed Cr isotope analyses for whole rocks and chemically separated phases of the new CM2 chondrite, Sutter's Mill (SM 43 and 51). The two whole rocks of Sutter's Mill show essentially identical ε⁵⁴Cr excesses (SM 43 = +0.95 ± 0.09ε, SM 51 = +0.88 ± 0.07ε), relative to the Earth. These values are the same within error with that of the CM2‐type Murchison (+0.89 ± 0.08ε), suggesting that parent bodies of Sutter's Mill and Murchison were formed from the same precursor materials in the solar nebula. Large ε⁵⁴Cr excess of up to 29.40ε is observed in the silicate phase of Sutter's Mill, while that of Murchison shows 15.74ε. Importantly, the leachate fractions of both Sutter's Mill and Murchison form a steep linear anticorrelation between ε⁵⁴Cr and ε⁵³Cr, cross‐cutting the positive correlation previously observed in carbonaceous chondrites. The fact that L4 acid leachate fraction contains higher ⁵⁴Cr excesses than that of L5 step designed to dissolve refractory minerals suggests that spinel is not a major ⁵⁴Cr carrier. We also note that L5 contains ⁵³Cr anomalies lower than the solar initial value, suggesting it carries a component of nucleosynthetic anomaly unrelated to the ⁵³Mn decay. We have identified five endmember components of nucleosynthetic origin among the early solar system materials.