Hydrogen isotopic composition of water from fossil micrometeorites in howardites

We have measured the hydrogen isotopic composition (D/H ratios) of the water from 13 carbonaceous chondritic microclasts (CCMs, size <1 mm) trapped in two howardites (Kapoeta and Yamato-793497) early in the evolution of Solar System. The division into tochilinite-rich; magnetite-rich, olivine-poor; magnetite-rich, olivine-rich CCM types is corroborated by the hydrogen isotopic compositions. Both mineralogy and hydrogen isotopic compositions demonstrate that tochilinite-rich CCMs represent CM2 chondritic matter. In contrast, there is no good match between the isotopic and mineralogical properties of the magnetite-rich CCMs and the known groups of carbonaceous chondrites, suggesting that magnetite-rich CCMs represent a new kind of chondritic matter, not yet sampled in meteorite collections. This demonstrates that the view of the asteroid belt revealed by the collection of meteorites is incomplete. The study of (micro)clasts offers a unique opportunity to better decipher the nature and relative abundance of asteroids.The average hydrogen isotopic composition of water belonging to CCMs, D/H = (152.0 ± 4.8) × 10⁻⁶ (1σ_m), is similar to that of Antarctic micrometeorites (AMMs), D/H = (161.2 ± 3.8) × 10⁻⁶ (1σ_m). The similarity, in terms of mineralogy and hydrogen isotopic composition, between CCMs and AMMs demonstrates that the composition of the micrometeorites has not been modified over the whole history of the Solar System. It indicates that the composition of the micrometeorite flux onto Earth has been, and is, dominated by a mixture of CM2-like; magnetite-rich, olivine-poor; magnetite-rich, olivine-rich carbonaceous chondritic matter exemplified by CCMs found in howardites. Because CCMs have not suffered atmospheric entry, they provide an abundant source of pristine micrometeorites.The average D/H ratio of the whole population of CCMs is identical within errors to that of the Earth (149 ± 3 × 10⁻⁶). The match between the CCMs D/H ratio and that of the Earth is especially remarkable because 1) three different populations of CCMs are needed to make the D/H ratio of the Earth; 2) there is no single carbonaceous chondrite group for which a similar match exists. This observation suggests that CCMs population might be representative of the late veneer agent(s) that delivered water to the Earth.     

Chondritic lithic clasts in the CB/CH-like meteorite Isheyevo: Fragments of previously unsampled parent bodies

The CB/CH-like chondrite Isheyevo is characterized by the absence of fine-grained interchondrule matrix material; the only present fine-grained material is found as chondritic lithic clasts. In contrast to the pristine high-temperature components of Isheyevo, these clasts experienced extensive aqueous alteration in an asteroidal setting. Hence, the clasts are foreign objects that either accreted together with the high-temperature components or were added later to the final Isheyevo parent body during regolith gardening. In order to constrain the origin and secondary alteration of the clasts in Isheyevo, we studied their mineralogy, petrography, structural order of the polyaromatic carbonaceous matter, and oxygen isotopic compositions of carbonates. Three main groups of clasts were defined based on mineralogy and petrology. Group I clasts consist of phyllosilicates, carbonates, magnetite, and lath-shaped Fe,Ni-sulfides. Group II clasts contain different abundances of anhydrous silicates embedded in a hydrated matrix; sulfides, magnetite, and carbonates are rare. With only a few exceptions, groups I and II clasts did not experienced significant thermal metamorphism. Group III clasts are characterized by the absence of magnetite and the presence of Fe,Ni-metal. In addition to aqueous alteration, they experienced thermal metamorphism as reflected by the structure of their polyaromatic carbonaceous matter. While there are some similarities between the Isheyevo clasts, CI chondrites, and the matrices of CM and CR chondrites, on the whole, the characteristics of the clasts do not match those of any of these aqueously altered meteorite classes. Nor do they match those of similar material in various types of chondritic clasts present in other meteorite groups. We conclude that the Isheyevo clasts represent fragments of previously unsampled parent bodies.     

Formation of the Bencubbin polymict meteoritic breccia

The Bencubbin meteorite is a polymict breccia consisting of a host fraction of ~60% metal and ~40% ferromagnesian silicates and a selection of carbonaceous, ordinary and ‘enstatite’ chondritic clasts. Concentrations of 27 elements were determined by neutron activation in replicate samples of the host silicates and the ordinary and carbonaceous chondritic clasts; 12 elements were determined in the host metal. Compositional data for the ordinary chondrite clast indicate a classification of LL4 ± 1. Refractory element data for the carbonaceous chondrite clast indicate that it belongs to the CI-CM-CO clan; its volatile element abundances are intermediate between those of CM and CO chondrites. Abundances of nonvolatile elements in the silicate host are similar to those in the carbonaceous chondrite clast and in CM chondrites; the rare earths are unfractionated. We conclude that it is not achondritic as previously designated, but chondritic and that it is probably related to the CI-CM-CO clan; its volatile abundances are lower than those in CO chondrites. Oxygen isotope data are consistent with these classifications. Host metal in Bencubbin and in the closely related Weatherford meteorite has low abundances of moderately volatile siderophiles; among iron meteorite groups its nearest relative is group IIIF.We suggest that Bencubbin and Weatherford formed as a result of an impact event on a carbonaceous chondrite regolith. The impact generated an ‘instant magma’ that trapped and surrounded regolithic clasts to form the polymict breccia. The parent of this ‘magma’ was probably the regolith itself, perhaps mainly consisting of the so-called ‘enstatite’ chondrite materials. Accretion of such a variety of materials to a small parent body was probably only possible in the asteroid belt.     

Meteorite ablation products and their contribution to the atmospheres of terrestrial planets: An experimental study using pyrolysis-FTIR

We have used a recently developed quantitative pyrolysis-Fourier transform infrared spectroscopy method to measure the production of water and carbon dioxide during 250 °C desorption and 1000 °C gasification steps for a range of carbonaceous chondrites. Greater yields of water and carbon dioxide during gasification are associated with meteorites believed to have experienced more aqueous alteration on their asteroid parent body (i.e. gas yields for petrographic type 1 > type 2 > type 3). Volatile yields most likely reflect quantities of hydrated mineral phases and partially oxidised organic matter. Methane was not detected in the gasification products of the meteorites, allowing an upper limit on its production of around 100 ppm to be calculated based on the sensitivity of the pyrolysis-Fourier transform infrared spectroscopy technique employed. When considered alongside rates of infall of cosmic dust throughout Earth history, the data can be used to evaluate the production of volatiles during the thermal ablation of dust upon atmospheric entry, and to estimate their contribution to a terrestrial planet’s atmosphere and hydrosphere. Over the long term, it appears that contributions of this nature to the Earth’s volatile inventory are small, although production rates are calculated to have been substantially higher before and during the Late Heavy Bombardment of 3.8-4.0 Ga. Moreover, ablation of carbonaceous chondritic material does not appear to be a plausible source of the atmospheric methane budget of Mars.     

Oxygen isotopic composition of chondritic interplanetary dust particles: A genetic link between carbonaceous chondrites and comets

Oxygen isotopes were measured in four chondritic hydrated interplanetary dust particles (IDPs) and five chondritic anhydrous IDPs including two GEMS-rich particles (Glass embedded with metal and sulfides) by a combination of high precision and high lateral resolution ion microprobe techniques.All IDPs have isotopic compositions tightly clustered around that of solar system planetary materials. Hydrated IDPs have mass-fractionated oxygen isotopic compositions similar to those of CI and CM carbonaceous chondrites, consistent with hydration of initially anhydrous protosolar dust. Anhydrous IDPs have small ¹⁶O excesses and depletions similar to those of carbonaceous chondrites, the largest ¹⁶O variations being hosted by the two GEMS-rich IDPs. Coarse-grained forsteritic olivine and enstatite in anhydrous IDPs are isotopically similar to their counterparts in comet Wild 2 and in chondrules suggesting a high temperature inner solar system origin. The small variations in the ¹⁶O content of GEMS-rich IDPs suggest that most GEMS either do not preserve a record of interstellar processes or the initial interstellar dust is not ¹⁶O-rich as expected by self-shielding models, although a larger dataset is required to verify these conclusions.Together with other chemical and mineralogical indicators, O isotopes show that the parent-bodies of carbonaceous chondrites, of chondritic IDPs, of most Antarctic micrometeorites, and comet Wild 2 belong to a single family of objects of carbonaceous chondrite chemical affinity as distinct from ordinary, enstatite, K- and R-chondrites. Comparison with astronomical observations thus suggests a chemical continuum of objects including main belt and outer solar system asteroids such as C-type, P-type and D-type asteroids, Trojans and Centaurs as well as short-period comets and other Kuiper Belt Objects.     

The contribution of sulphur dioxide from ablating micrometeorites to the atmospheres of Earth and Mars

Atmospheric composition is a key control on climate and the habitability of planetary surfaces. Ablation of infalling micrometeorites has been recognised as one way in which atmospheric chemistry can be changed, especially at times in solar system history when the infall rates of exogenous material were high. Despite its potential to influence climate and habitability, extraterrestrial sulphur dioxide is currently an unquantified contribution to the atmospheres of the terrestrial planets. We have used flash pyrolysis to simulate the atmospheric entry of micrometeorites and Fourier-transform infrared spectroscopy to identify and quantify the sulphur dioxide produced from the carbonaceous meteorites Orgueil (CI1), ALH 88045 (CM1), Cold Bokkeveld (CM2), Murchison (CM2) and Mokoia (CV3). We have used this approach to understand the introduction of sulphur dioxide to the atmospheres of Earth and Mars from infalling micrometeorites. Sulphates, present in carbonaceous chondrites at a few wt.%, are resistant to thermal decomposition, limiting the yields of sulphur dioxide from unmelted micrometeorites. Infalling micrometeorites are a minor source of present-day sulphur dioxide on Earth and Mars, calculated to be up to around 2400 tonnes and about 350 tonnes, respectively. During the Late Heavy Bombardment (LHB), the much greater infall rates of micrometeoritic dust are calculated to be associated with average production rates of sulphur dioxide of around 20 Mt yr⁻¹ for the early Earth and 0.5 Mt yr⁻¹ for early Mars, for a LHB of 100 Myr. These rates of delivery of sulphur dioxide at high altitudes would have reduced the solar energy reaching the surfaces of these planets, via scattering of sunlight by stratospheric sulphate aerosols, and may have had detrimental effects on developing biospheres by promoting cooler climates and reducing the probability of liquid water on planetary surfaces.     

Oxygen isotope measurements of individual unmelted Antarctic micrometeorites

We present oxygen isotope measurements of 28 unmelted Antarctic micrometeorites measuring 150-250 μm (long axis) collected in the South Pole water well. The micrometeorites were all unmelted and classified as either fine-grained, scoriaceous, coarse-grained or composite (a mix of two other classes). Spot analyses were made of each micrometeorite type using an ion microprobe. The oxygen isotope values were measured relative to standard mean ocean water (SMOW) and range from δ¹⁸O = 3‰ to 60‰ and δ¹⁷O = −1‰ to 32‰, falling along the terrestrial fractionation line (TFL) within 2σ errors. Several analytical spots (comprising multiple phases) were made on each particle. Variability in the oxygen isotope ratios was observed among micrometeorite types, between micrometeorites of the same type and between analytical spots on a single micrometeorite indicating that micrometeorites are isotopically heterogeneous. In general, the lowest isotope values are associated with the coarse-grained micrometeorites whereas most of the fine-grained and scoriaceous micrometeorites have an average δ¹⁸O ? 22‰, suggesting that the matrix in micrometeorites is isotopically heavier than the anhydrous silicate phases. The oxygen isotope values for the coarse-grained micrometeorites, composed mainly of anhydrous phases, do not lie along the carbonaceous chondrite anhydrous mineral (CCAM) line, as observed for olivines, pyroxenes and some kinds of chondrules in carbonaceous chondrites, suggesting that coarse-grained MMs are not related to chondrules, as previously thought. Our measurements span the same range as values found for melted micrometeorites in other studies. Although four of the micrometeorites have oxygen isotope values lying along the TFL, close to the region where the bulk CI carbonaceous chondrites are found, 21 particles have very enriched ¹⁷O and ¹⁸O values that have not been reported in previous analyses of chondrite matrix material, suggesting that they could be a new type of Solar System object. The parent bodies of the micrometeorites with higher ¹⁸O values may be thermal metamorphosed carbonaceous asteroids that have not been found as meteorites either because they are friable asteroids that produce small particles rather than rocks upon collision with other bodies, or because the rocks they produce are too friable to survive atmospheric entry.     

The Kaidun chondrite breccia: Petrology, oxygen isotopes, and trace element abundances

Oxygen isotope and trace element data for 13 samples of the Kaidun chondritic breccia reaffirm the complex polymict nature of this unique meteorite. Bulk Kaidun samples most closely resemble CR chondrites, but the matrix is CI-like. Two separated clasts are CR-like but have some properties that resemble CM, two clasts are enstatite chondrites (one EL and one EH), one clast is an aubrite-like metal-rich impact melt, and one clast is a unique layered olivine-bearing pyroxenite with the isotopic composition of an aubrite. Yet, although each clast resembles a known meteorite group, all deviate in some respect from the norms for those groups. Collectively, Kaidun has sampled materials not yet represented in the world meteorite collections and which greatly extend the definitions of known meteorite groups. Phyllosilicates in Kaidun span a very wide range in composition and vary from clast to clast, suggesting that the aqueous alteration experienced by the clasts predated assembly of the Kaidun parent body.     

Effects of secondary alteration on the composition of free and IOM-derived monocarboxylic acids in carbonaceous chondrites

Monocarboxylic acids (MCAs) are important astrobiologically because they are often the most abundant soluble compounds in carbonaceous chondrites (CCs) and are potential synthetic end products for many biologically important compounds. However, there has been no systematic study on the effect of parent body alteration on molecular and isotopic variability of MCAs. Since MCAs in meteorites are dominated by low molecular weight (C1-C8), highly volatile compounds, their distributions are likely to be particularly sensitive to secondary alteration processes. In contrast, the aliphatic side chains of insoluble organic matter (IOM) in CCs, whose composition has been shown to be closely related to the MCAs, may be far more resistant to secondary alteration. In the present study, we determined the distributions and isotopic ratios of free and IOM-derived MCAs in six carbonaceous chondrites with a range of classifications: Murchison (CM2), EET 87770 (CR2), ALH 83034 (CM1), ALH 83033 (CM2), MET 00430 (CV3) and WIS 91600 (C2). We compare mineralogical and petrological characteristics to the MCAs distributions to better define the processes leading to the synthesis and alteration of meteoritic MCAs. Our results show that aqueous and especially thermal alteration in the parent bodies led to major loss of free MCAs and depletion of straight relative to branched chain compounds. However, the MCAs derived from aliphatic side chains of IOM are well preserved despite of secondary alterations. The molecular and isotopic similarities of IOM-derived MCAs in different chondrite samples indicate very similar synthetic histories for organic matter in different meteorites.     

Relict silicate inclusions in extraterrestrial chromite and their use in the classification of fossil chondritic material

Chromite is the only common meteoritic mineral surviving long-term exposure on Earth, however, the present study of relict chromite from numerous Ordovician (470 Ma) fossil meteorites and micrometeorites from Sweden, reveals that when encapsulated in chromite, other minerals can survive for hundreds of millions of years maintaining their primary composition. The most common minerals identified, in the form of small (<1-10 μm) anhedral inclusions, are olivine and pyroxene. In addition, sporadic merrillite and plagioclase were found.Analyses of recent meteorites, holding both inclusions in chromite and corresponding matrix minerals, show that for olivine and pyroxene inclusions, sub-solidus re-equilibration between inclusion and host chromite during entrapment has led to an increase in chromium in the former. In the case of olivine, the re-equilibration has also affected the fayalite (Fa) content, lowering it with an average of 14% in inclusions. For Ca-poor pyroxene the ferrosilite (Fs) content is more or less identical in inclusions and matrix. By these studies an analogue to the commonly applied classification system for ordinary chondritic matrix, based on Fa in olivine and Fs in Ca-poor pyroxene, can be established also for inclusions in chromite. All olivine and Ca-poor pyroxene inclusions (>1.5 μm) in chromite from the Ordovician fossil chondritic material plot within the L-chondrite field, which is in accordance with previous classifications. The concordance in classification together with the fact that inclusions are relatively common makes them an accurate and useful tool in the classification of extraterrestrial material that lacks matrix silicates, such as fossil meteorites and sediment-dispersed chromite grains originating primarily from decomposed micrometeorites but also from larger impacts.     

Origin of ureilites inferred from a SIMS oxygen isotopic and trace element study of clasts in the Dar al Gani 319 polymict ureilite

Secondary ion mass spectrometer (SIMS) oxygen isotope analyses were performed on 24 clasts, representing 9 clast types, in the Dar al Gani (DaG) 319 polymict ureilite with precisions better than 1‰. Olivine-rich clasts with typical ureilitic textures and mineral compositions have oxygen isotopic compositions that are identical to those of the monomict ureilites and plot along the CCAM (Carbonaceous Chondrite Anhydrous Mineral) line. Other igneous clasts, including plagioclase-bearing clasts, also plot along the CCAM line, indicating that they were derived from the ureilite parent body (UPB). Thus, we suggest that some of the plagioclase-bearing clasts in the polymict ureilites represent the “missing basaltic component” produced by partial melting on the UPB.Trace element concentrations (Mg, K, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Rb, Sr and Ba) in ureilitic plagioclase and glass from 13 clasts were obtained by using the SIMS high mass resolution method. The trace element contents of the plagioclase generally show monotonic variations with anorthite content (mol%) that are consistent with partial melting and fractional crystallization. Incompatible trace element concentrations (K, Ti, and Ba) are low and variable for plagioclase with An > 40, indicating that the parental magmas for some clasts were derived from a depleted source. We performed partial melt modeling for CI and CM precursor compositions and compared the results to the observed trace element (K, Ba, and Sr) abundances in the plagioclase. Our results indicate that (1) the UPB evolved from a alkali-rich carbonaceous chondritic precursor, (2) parent melts of porphyritic clasts could have formed by 5-20% equilibrium partial melting and subsequent fractional crystallization, and (3) parent melts of the incompatible trace element-depleted clasts could be derived from fractional melting, where low degree (<10%) partial melts were repeatedly extracted from their solid sources.Thus, both the oxygen isotopic and trace element compositions of the plagioclase bearing clasts in DaG-319 suggest that the UPB underwent localized low degree-partial melting events. The partial melts could have been repeatedly extracted from the precursor, resulting in the formation of the olivine-pigeonite monomict ureilites as the final residue.     

NMR studies of chemical structural variation of insoluble organic matter from different carbonaceous chondrite groups

Solid-state ¹H and ¹³C Nuclear Magnetic Resonance (NMR) spectroscopic experiments have been performed on isolated meteoritic Insoluble Organic Matter (IOM) spanning four different carbonaceous chondrite meteorite groups; a CR2 (EET92042), a CI1 (Orgueil), a CM2 (Murchison), and the unique C2 meteorite, Tagish Lake. These solid state NMR experiments reveal considerable variation in bulk organic composition across the different meteorite group’s IOM. The fraction of aromatic carbon increases as CR2 < CI1 < CM2 < Tagish Lake. The increases in aromatic carbon are offset by reductions in aliphatic (sp³) carbon moieties, e.g., “CH_x,” and “CH_x(O,N).” Oxidized sp² bonded carbon, e.g., carboxyls and ketones grouped as “CO,” are largely conservative across these meteorite groups. Single pulse (SP) ¹³C magic angle spinning (MAS) NMR experiments reveal the presence of nanodiamonds with an apparent concentration ranking in the IOM of CR2 < CI1 < CM2 < Tagish Lake. A pair of independent NMR experiments reveals that, on average, the aromatic moieties in the IOM of all four meteoritic IOM fractions are highly substituted. Fast spinning SP ¹H MAS NMR spectral data combined with other NMR experimental data reveal that the average hydrogen content of sp³ bonded carbon functional groups is low, requiring a high degree of aliphatic chain branching in each IOM fraction. The variation in chemistry across the meteorite groups is consistent with alteration by low temperature chemical oxidation. It is concluded that such chemistry principally affected the aliphatic moieties whereas the aromatic moieties and nanodiamonds may have been largely unaffected.     

Evaluating the thermal metamorphism of CM chondrites by using the pyrolytic behavior of carbonaceous macromolecular matter

The degrees of thermal metamorphism of 10 CM chondrites and of the Allende CV3 chondrite were evaluated from the viewpoint of “graphitization” of the carbonaceous macromolecular matter by means of flash pyrolysis-gas chromatography (GC). The unheated chondrites, Yamato- (Y-) 791198, Murray and Cold Bokkeveld, yielded larger amounts and wider varieties of pyrolyzates than the chondrites strongly heated in the parent asteroids, Y-82054, Y-86695, and Belgica- (B-) 7904, and Asuka- (A-) 881334 (more strongly heated than Y-793321, which has been weakly heated, but lesser than the other strongly heated meteorites). The weakly heated chondrites, Y-793321 and A-881458, showed intermediate features. The data indicate that graphitization of the carbonaceous matter is most extreme in the strongly heated chondrites and that during graphitization, the matter has lost its labile portion, which can generate pyrolyzates such as naphthalene. In order to establish a new method for the evaluation of the degree of graphitization of chondritic carbonaceous matter, a diagram was developed to show the relationship between the total amounts of pyrolyzates with retention times later than 5 min (=S_RT>5) and the ratio of the amount of naphthalene, a pyrolysis product, to S_RT>5 (=S_N/S_RT>5). The diagram indicates a possible evolutionary pathway of graphitization of the carbonaceous matter in carbonaceous chondrites.     

A depleted, not ideally chondritic bulk Earth: The explosive-volcanic basalt loss hypothesis

It has long been customary to assume that in the bulk composition of the Earth, all refractory-lithophile elements (including major oxides Al₂O₃ and CaO, all of the REE, and the heat-producing elements Th and U) occur in chondritic, bulk solar system, proportion to one another. Recently, however, Nd-isotopic studies (most notably Boyet M. and Carlson R. W. (2006) A new geochemical model for the Earth’s mantle inferred from ¹⁴⁶Sm-¹⁴²Nd systematics. Earth Planet. Sci. Lett.250, 254-268) have suggested that at least the outer portion of the planet features a Nd/Sm ratio depleted to ∼0.93 times the chondritic ratio. The primary reaction to this type of evidence has been to invoke a “hidden” reservoir of enriched matter, sequestered into the deepest mantle as a consequence of primordial differentiation. I propose a hypothesis that potentially explains the evidence for Nd/Sm depletion in a very different way. Among the handful of major types of differentiated asteroidal meteorites, two (ureilites and aubrites) are ultramafic restites so consistently devoid of plagioclase that meteoriticists were once mystified as to how all the complementary plagioclase-rich matter (basalt) was lost. The explanation appears to be basalt loss by graphite-fueled explosive volcanism on roughly 100-km sized planetesimals; with the dispersiveness of the process dramatically enhanced, relative to terrestrial experience, because the pyroclastic gases expand into vacuous space (Wilson L. and Keil K. (1991) Consequences of explosive eruptions on small Solar System bodies: the case of the missing basalts on the aubrite parent body. Earth Planet. Sci. Lett.104, 505-512). By analogy with lunar pyroclastic products, the typical size of pyroclastic melt/glass droplets under these circumstances will be roughly 0.1 mm. Once separated from an asteroidal or planetesimal gravitational field, droplets of this size will generally spiral toward the Sun, rather than reaccrete, because drag forces such the Poynting-Robertson effect quickly modify their orbits (the semimajor axis, in a typical scenario, is reduced by several hundred km during the first trip around the Sun). Assuming a similar process occurred on many of the Earth’s precursor planetesimals while they were still roughly 100 km in diameter, the net effect would be a depleted composition for the final Earth. I have modeled the process of trace-element depletion in the planetesimal mantles, assuming the partial melting was nonmodal and either batch or dynamic in terms of the melt-removal style. Assuming the process is moderately efficient, typical final-Earth Nd/Sm ratios are 0.93-0.96 times chondritic. Depletion is enhanced by a relatively low assumed residual porosity in batch-melting scenarios, but dampened by a relatively high value for “continuous” residue porosity in dynamic melting scenarios. Pigeonite in the source matter has a dampening effect on depletion. There are important side effects to the Nd/Sm depletion. The heat-producing elements, Th, U and K, might be severely depleted. The Eu/Eu^∗ ratio of the planet is unlikely to remain precisely chondritic. One of the most inevitable side effects, depletion of the Al/Ca ratio, is consistent with an otherwise puzzling aspect of the composition of the upper mantle. A perfectly undepleted composition for the bulk Earth is dubious.     

The composition and origin of metal in howardites

Howardites can be divided into two main groups, Ni-rich (>350ppm Ni) and Ni-poor (<150ppm Ni). In the Ni-rich group Ni occurs principally in metal grains associated with melt rocks and is largely derived from projectiles which caused the melting. The metal in Bununu, Kapoeta and Malvern melt rocks plots in the meteoritic Ni-Co range and in Bununu and Kapoeta is enriched in P. By contrast, most metal grains in primary lithic and crystal clasts in howardites are Ni-poor and plot mainly in the composition field of pristine lunar anorthosite metal. However, there are variations in the abundance and exact composition of primary metal from howardite to howardite and each therefore represents a discrete source region. The matrix metal in Bholgati, Bununu, and Kapoeta shows the diversity of compositions expected in a polymict breccia, with compositions plotting in and between the anorthositic and meteoritic Ni-Co fields. Other howardites show a more limited range of matrix metal compositions, because of limited metal-bearing clasts.Petersburg differs from other howardites in several ways. The metal in primary clasts has a unique $\text{Ni}\text{Co}$ ratio of about 40, which indicates derivation from a different reservoir from other howardite primary clasts. The metal in the matrix consists of large grains intergrown with silicates with compositions clustering tightly at 3.3% Ni, 0.2% Co. This is interpreted as equilibration, possibly as the result of deeper burial for Petersburg than for other howardites.     

Carbonaceous chondrites—II. Carbonaceous chondrite phyllosilicates and light element geochemistry as indicators of parent body processes and surface conditions

Petrographic observations and analyses of CM matrices are consistent with their origin as in situ low temperature (<400°K) aqueous alteration products in a parent body regolith. At least four different phyllosilicates were tentatively characterized in Murray and Murchison meteorites, in addition to Fe- and Mg-serpentines in Nogoya. In comparison with bulk meteorite compositions, all phyllosilicates and bulk matrices show enrichment of K relative to Na. Possible loss of Na and possibly some Cl, with addition of H₂O and CO₂ and water-soluble organic compounds during alteration, indicates a partially open system during alteration. Poorly characterized phases (PCP) are fine-grained (< 1 μm) admixtures of variable proportions of phyllosilicates, carbonaceous matter and opaque oxides of sulfur with high Fe, Ni and Cr contents. Calcite and some magnetite show paragenetic overlap with PCP and phyllosilicates. Carbonaceous matter is largely associated with PCP in altered CM matrices. In the unaltered CV Allende, carbonaceous matter is concentrated on olivine surfaces as a micromounded coating, particularly in the dark haloes that surround some chondrules and aggregates. Precursive alteration material may have been analogous to similarly coated olivine mixed with smaller amounts of metal and sulfides.Synthesis of the water soluble organic compounds found in CM matrices may have occurred prior to or in the same environment as did aqueous alteration of the precursive phases. Preservation or partial preservation of this organic matter may reflect the degree of overlap in episodes of synthesis and alteration.Nogoya is 95% altered and has a bulk carbon content of 5.2 wt%, which is higher than any meteorite. In addition, it has the lowest measured ${}^{13}\text{C}{}^{12}\text{C}$ ratio of any other carbonaceous chondrite, except for Karoonda.     

Uranium and thorium in achondrites

The abundances of U and Th in 19 achondrites and two pallasite olivines have been measured by radiochemical neutron activation analysis. Brecciated eucrites are enriched relative to chondrites in both elements by factors between 10 and 20, perhaps as a result of a magmatic differentiation process. Two unbrecciated eucrites are far less enriched, possibly due to their origin as igneous cumulates. The diogenites Johnstown and Shalka contain approximately chondritic levels of U and Th, but Ellemeet is 10 times lower. The abundances in three howardites are in good agreement with those expected from major element data for a mixing model with eucrite and diogenite end members. The high O¹⁸ basaltic achondrites Nakhla, Shergotty and Angra dos Reis have a range of U and Th abundances similar to the brecciated eucrites and howardites, but have systematically higher Th/U ratios. The Bishopville aubrite has U and Th abundances and Th/U ratios similar to those of several enstatite chondrites, suggesting a genetic relationship. The Norton County aubrite has a low Th/U, similar to that observed in recrystallized and metamorphosed terrestrial ultrabasic rocks, indicating a more complex history. Pallasite olivines have low U and Th contents (0.5.4 ppb and 1.4.3 ppb, respectively) similar to those in terrestrial dunites. The Goalpara ureilite has very low U (<0–6 ppb) and Th (2.7 ppb) abundance consistent with an origin from carbonaceous chondrites by partial melting.     

Geo- and cosmochemistry of the twin elements yttrium and holmium

We have analyzed the Y/Ho-ratios in bulk chondrites, chondrules and four Ca- and Al-rich inclusions (CAIs) from carbonaceous and unequilibrated ordinary and enstatite chondrites (EC) by laser ablation inductively coupled mass spectrometry (LA-ICPMS). We demonstrate that bulk rock sample preparation by containerless melting is a suitable method for preparation of bulk rock samples for high-precision LA-ICPMS. Bulk chondrites have variable Y/Ho-ratios. Carbonaceous chondrites (CI1, CM2, CV3, and CK4) have a common Y/Ho-ratio (25.94 ± 0.08, 2σ) that is regarded as the solar system Y/Ho-ratio. The Y/Ho-ratio increases from carbonaceous, through ordinary (LL, L, H) to enstatite chondrites (EL6), which show the highest Y/Ho-ratio of 27.25. We discuss the result with respect to the origin of fractionation of Re and Os between chondrite groups. Within analytical error, Y and Ho show a good correlation in OC and CV3 chondrules and define an Y/Ho-ratio of 26.22 ± 0.40 (2σ). Y/Ho-fractionation in Ca- and Al-rich inclusions is related to differences in volatility. The bulk silicate Earth is suggested to have a solar Y/Ho-ratio and links the Earth with carbonaceous chondrites. Y/Ho variations in primitive and differentiated terrestrial igneous rocks are discussed in framework of incompatibility of Y and Ho during partial melting. Applicability of Y/Ho as tracer for or against a sedimentary origin of the putative host rock of the Earth’s oldest traces of life from the island of Akilia is briefly discussed.     

L'Olivine dans les howardites: origine,et implications pour le corps parent de ces météorites achondritiques

Electron microprobe analyses have been performed on 300 olivine grains found in 11 howardites. The olivine compositions almost continuously range from Fa 8 to Fa 89 with two prominent populations at Fa 13 and Fa 30. The tail of the fayalite contents distribution may correspond to the succession of several small clusters of Fe-rich olivine grains. Most howardites have olivine populations in common that would result from the fragmentation of different rocks of the howardites parent body. The distribution of the olivine grains between several groups of different $\text{FeO}\text{MnO}$ ratios indicates olivine crystallization from distinct magmas. The chemical characteristics of the olivines of the pallasites, diogenites and mesosiderites are found among the olivines of the howardites and suggests a common parent body for these different types of meteorites. The differentiation model of the eucrites parent body proposed by Stolper (1977) is extended to the partial fusion of distinct assemblages silicates + metal which could proceed from recrystallizations, under different oxidation-reduction conditions, of a primordial chondritic material depleted in volatile elements.