Solar System Processes Research Articles

The initial abundance and distribution of 92Nb in the Solar System

Niobium-92 is an extinct proton-rich nuclide, which decays to 92Zr with a half-life of 37 Ma. This radionuclide potentially offers a unique opportunity to determine the timescales of early Solar System processes and the site(s) of nucleosynthesis for p-nuclei, once its initial abundance and distribution in the Solar System are well established. Here we present internal Nb–Zr isochrons for three basaltic achondrites with known U–Pb ages: the angrite NWA 4590, the eucrite Agoult, and the ungrouped achondrite Ibitira. Our results show that the relative Nb–Zr isochron ages of the three meteorites are consistent with the time intervals obtained from the Pb–Pb chronometer for pyroxene and plagioclase, indicating that 92Nb was homogeneously distributed among their source regions. The Nb–Zr and Pb–Pb data for NWA 4590 yield the most reliable and precise reference point for anchoring the Nb–Zr chronometer to the absolute timescale: an initial 92Nb/93Nb ratio of (1.4±0.5)×10−5 at 4557.93±0.36 Ma, which corresponds to a 92Nb/93Nb ratio of (1.7±0.6)×10−5 at the time of the Solar System formation. On the basis of this new initial ratio, we demonstrate the capability of the Nb–Zr chronometer to date early Solar System objects including troilite and rutile, such as iron and stony-iron meteorites. Furthermore, we estimate a nucleosynthetic production ratio of 92Nb to the p-nucleus 92Mo between 0.0015 and 0.035. This production ratio, together with the solar abundances of other p-nuclei with similar masses, can be best explained if these light p-nuclei were primarily synthesized by photodisintegration reactions in Type Ia supernovae.

The deuterium/hydrogen distribution in chondritic organic matter attests to early ionizing irradiation.

Primitive carbonaceous chondrites contain a large array of organic compounds dominated by insoluble organic matter (IOM). A striking feature of this IOM is the systematic enrichment in deuterium compared with the solar hydrogen reservoir. This enrichment has been taken as a sign of low-temperature ion-molecule or gas-grain reactions. However, the extent to which Solar System processes, especially ionizing radiation, can affect D/H ratios is largely unknown. Here, we report the effects of electron irradiation on the hydrogen isotopic composition of organic precursors containing different functional groups. From an initial terrestrial composition, overall D-enrichments and differential intramolecular fractionations comparable with those measured in the Orgueil meteorite were induced. Therefore, ionizing radiation can quantitatively explain the deuteration of organics in some carbonaceous chondrites. For these meteorites, the precursors of the IOM may have had the same isotopic composition as the main water reservoirs of the inner Solar System.

PALLADIUM ISOTOPIC EVIDENCE FOR NUCLEOSYNTHETIC AND COSMOGENIC ISOTOPE ANOMALIES IN IVB IRON METEORITES

The origin of ubiquitous nucleosynthetic isotope anomalies in meteorites may represent spatial and/or temporal heterogeneity in the sources that supplied material to the nascent solar nebula, or enhancement by chemical processing. For elements beyond the Fe peak, deficits in s-process isotopes have been reported in some (e.g., Mo, Ru, W) but not all refractory elements studied (e.g., Os) that, among the iron meteorites, are most pronounced in IVB iron meteorites. Palladium is a non-refractory element in the same mass region as Mo and Ru. In this study, we report the first precise Pd isotopic abundances from IVB irons to test the mechanisms proposed for the origin of isotope anomalies. First, this study determined the existence of a cosmogenic neutron dosimeter from the reaction 103Rh(n, beta-)104Pd in the form of excess 104Pd, correlated with excess 192Pt, in IVB irons. Second, all IVB irons show a deficit of the s-process only isotope 104Pd (\varepsilon 104Pd = -0.48 ± 0.24), an excess of the r-only isotope 110Pd (\varepsilon 110Pd = +0.46 ± 0.12), and no resolvable anomaly in the p-process 102Pd (\varepsilon 102Pd = +1 ± 1). The magnitude of the Pd isotope anomaly is about half that predicted from a uniform depletion of the s-process yields from the correlated isotope anomalies of refractory Mo and Ru. The discrepancy is best understood as the result of nebular processing of the less refractory Pd, implying that all the observed nucleosynthetic anomalies in meteorites are likely to be isotopic relicts. The Mo-Ru-Pd isotope systematics do not support enhanced rates of the 22Ne(alpha,n)25Mg neutron source for the solar system s-process.

Interstellar and Solar System organic matter preserved in interplanetary dust

AbstractInterplanetary dust particles (IDPs) collected in the Earths stratosphere derive from collisions among asteroids and by the disruption and outgassing of short-period comets. Chondritic porous (CP) IDPs are among the most primitive Solar System materials. CP-IDPs have been linked to cometary parent bodies by their mineralogy, textures, C-content, and dynamical histories. CP-IDPs are fragile, fine-grained (< um) assemblages of anhydrous amorphous and crystalline silicates, oxides and sulfides bound together by abundant carbonaceous material. Ancient silicate, oxide, and SiC stardust grains exhibiting highly anomalous isotopic compositions are abundant in CP-IDPs, constituting 0.01-1% of the mass of the particles. The organic matter in CP-IDPs is isotopically anomalous, with enrichments in D/H reaching 50x the terrestrial SMOW value and 15N/14N ratios up to 3x terrestrial standard compositions. These anomalies are indicative of low T (10-100 K) mass fractionation in cold molecular cloud or the outermost reaches of the protosolar disk. The organic matter shows distinct morphologies, including sub-um globules, bubbly textures, featureless, and with mineral inclusions. Infrared spectroscopy and mass spectrometry studies of organic matter in IDPs reveals diverse species including aliphatic and aromatic compounds. The organic matter with the highest isotopic anomalies appears to be richer in aliphatic compounds. These materials also bear similarities and differences with primitive, isotopically anomalous organic matter in carbonaceous chondrite meteorites. The diversity of the organic chemistry, morphology, and isotopic properties in IDPs and meteorites reflects variable preservation of interstellar/primordial components and Solar System processing. One unifying feature is the presence of sub-um isotopically anomalous organic globules among all primitive materials, including IDPs, meteorites, and comet Wild-2 samples returned by the Stardust mission. We will present an overview of the current state of understanding of the properties and origins of organic matter in primitive IDPs.

A Novel Hybrid Ultramicrotomy\FIB-SEM Technique: Preparation of Serial Electron-Transparent Thin Sections of a Hayabusa Grain

The Japanese space agency's (JAXA) Hayabusa mission returned the first particulate samples (typically <100micron) from the surface of an asteroid (25143 Itokawa). These precious samples provide important insights into early Solar System processes, but their sizes pose tremendous challenges to coordinated analysis using a variety of nano- and micro-beam techniques. The ability to glean maximal information from individual particles has become increasingly important and depends critically on sample preparation. We developed a hybrid technique combining traditional ultramicrotomy with focused ion beam (FIB) techniques, allowing for more thorough in situ investigations of grain surfaces and interiors. Using this method, we increase the number of FIB-prepared sections that can be recovered from a particle with dimensions on the order of tens of microns. These sections can be subsequently analyzed using a variety of analytical techniques. Particle RA-QD02-0211 is a approx. 40×40×20 micron particle from Itokawa containing olivine and Fe sulfides. It was embedded in low viscosity epoxy and partly sectioned to a depth of approx 10 micron; sections are placed on Cu grids with thin amorphous films for transmission electron microscope (TEM) analyses. With the sample surface partly exposed, the epoxy bullet is trimmed to a height of approx. 5mm to accommodate the allowable dimensions for FIB work (FEI Quanta 600 3D dual beam FIB-SEM). Using a diamond trim knife, the epoxy surrounding the grain is removed on 3 sides (to within a few microns of the grain); the depth of material removed extends well below the bottom of the particle. The sample is attached to an SEM pin mount, the epoxy coated with conductive paint, and the entire assembly coated with approx. 40nm of carbon to eliminate sample charging during FIB work. A protective carbon cap is placed according to the plan for the 15 FIB sections. The central 'spine' of the cap runs perpendicular to the front of the sample, and the 'ribs' protruding from either side run parallel. Each rib indicates the location of a planned FIB section, and the spine contains the final two planned sections. We use a cap with a 4 micron-wide spine and 2micron-wide ribs that have ≳3.5 micron of space between them (narrower cuts result in too much re-deposition of material inside the trenches). Using a 30kV, 3nA ion-beam we expose the front surface of the grain and commence milling trenches between sections. Rather than using the typical C-cut to prepare the sample for lift-out, an L-cut is used instead, leaving the sample connected by an interior tab. tab. Sections are lifted out, attached to TEM grids and thinned to electron transparency. TEM analyses show that our hybrid technique preserves both interior and edge features, including surface modifications from exposure to the space environment, such as damaged rims that form in response to solar wind implantation effects and adhering grains. In addition, the FIB sections provide larger areas that are free of fractures and chatter effects in comparison to the microtome thin sections, thus enabling more accurate measurements of solar flare particle track densities that are used to determine the surface exposure age of the particles.

The Mg isotope composition of presolar silicate grains from red giant stars

We report O and Mg isotope compositions of presolar silicate grains which likely formed around asymptotic giant branch stars. Our grains represent the most abundant Mg-rich presolar grain group and their Mg isotope composition provides thus far missing information about the contribution of isotopically anomalous presolar dust to the Mg isotope inventory of the early Solar System.Presolar silicate grains were identified in situ, using the NanoSIMS, in the matrix of the ungrouped carbonaceous chondrite Acfer 094. O isotope compositions suggest that the presolar grains of the present study formed in the stellar winds of low mass (M⩽∼2.2×Msolar) red giant or asymptotic giant branch stars of close-to-solar metallicity and thus belong to the most abundant presolar silicate grain group.In order to minimise matrix contributions during spatially poorly resolved Mg isotope analyses (spatial resolution comparable to average grain size), meteorite matrix in the presolar grains’ vicinity was removed using a focussed Ga ion beam. To monitor accuracy, we prepared and analysed O-isotopically regular (Solar System) matrix grains the same way as the presolar grains. The 25Mg/24Mg ratios of all seven successfully analysed presolar silicate grains are identical to that of the Solar System at the precision of our measurements. The 26Mg/24Mg ratios of five grains are also solar but two grains have significant positive anomalies in 26Mg/24Mg. On average, however, 25Mg/24Mg and 26Mg/24Mg ratios are higher than solar by a few %. All grain compositions are consistent with Galactic chemical evolution and, possibly, isotope fractionation caused by interstellar or Solar System processing (sputtering and/or recondensation). The grain with the strongest enrichment in 26Mg relative to 25Mg (δ25Mg=34±25‰, δ26Mg=127±25‰; where δxMg=1000×[(xMg/24Mg)grain/(xMg/24Mg)meteorite matrix)−1] with x=25 or 26; the reported uncertainty corresponds to 1σ), probably incorporated 26Al during grain condensation. Our and previously reported Mg isotope data on presolar oxide and silicate grains indicate that the isotopically anomalous O-rich dust component of the Solar System’s parent molecular cloud was heterogeneous with respect to Mg isotope compositions and probably had a higher 26Mg/24Mg ratio on average than that of the present-day Solar System.

GALACTIC CHEMICAL EVOLUTION AND SOLARs-PROCESS ABUNDANCES: DEPENDENCE ON THE13C-POCKET STRUCTURE

We study the s-process abundances (A > 90) at the epoch of the solar-system formation. AGB yields are computed with an updated neutron capture network and updated initial solar abundances. We confirm our previous results obtained with a Galactic Chemical Evolution (GCE) model: (i) as suggested by the s-process spread observed in disk stars and in presolar meteoritic SiC grains, a weighted average of s-process strengths is needed to reproduce the solar s-distribution of isotopes with A > 130; (ii) an additional contribution (of about 25%) is required in order to represent the solar s-process abundances of isotopes from A = 90 to 130. Furthermore, we investigate the effect of different internal structures of the 13C-pocket, which may affect the efficiency of the 13C(a, n)16O reaction, the major neutron source of the s-process. First, keeping the same 13C profile adopted so far, we modify by a factor of two the mass involved in the pocket; second, we assume a flat 13C profile in the pocket, and we test again the effects of the variation of the mass of the pocket. We find that GCE s-predictions at the epoch of the solar-system formation marginally depend on the size and shape of the 13C-pocket once a different weighted range of 13C-pocket strengths is assumed. We ascertain that, independently of the internal structure of the 13C-pocket, the missing solar-system s-process contribution in the range from A = 90 to 130 remains essentially the same.

Measurement of the33S(α,p)36Cl cross section: Implications for production of36Cl in the early Solar System

Short-lived radionuclides (SLRs) with lifetimes \tau < 100 Ma are known to have been extant when the Solar System formed over 4.5 billion years ago. Identifying the sources of SLRs is important for understanding the timescales of Solar System formation and processes that occurred early in its history. Extinct 36Cl (t_1/2 = 0.301 Ma) is thought to have been produced by interaction of solar energetic particles (SEPs), emitted by the young Sun, with gas and dust in the nascent Solar System. However, models that calculate SLR production in the early Solar System (ESS) lack experimental data for the 36Cl production reactions. We present here the first measurement of the cross section of one of the main 36Cl production reactions, 33S(\alpha,p)36Cl, in the energy range 0.70 - 2.42 MeV/A. The cross section measurement was performed by bombarding a target and collecting the recoiled 36Cl atoms produced in the reaction, chemically processing the samples, and measuring the 36Cl/Cl ratio of the activated samples with accelerator mass spectrometry (AMS). The experimental results were found to be systematically higher than the cross sections used in previous local irradiation models and other Hauser-Feshbach calculated predictions. However, the effects of the experimentally measured cross sections on the modeled production of 36Cl in the early Solar System were found to be minimal. Reactions channels involving S targets dominate 36Cl production, but the astrophysical event parameters can dramatically change each reactions' relative contribution.

Diffusive fractionation of carbon isotopes in γ-Fe: Experiment, models and implications for early solar system processes

Carbon is an abundant element of planets and meteorites whose isotopes provide unique insights into both organic and inorganic geochemical processes. The identities of carbonaceous phases and their textural and isotopic characters shed light on dynamical processes in modern Earth systems and the evolution of the early solar system. In meteorites and their parent bodies, reduced carbon is often associated with Fe–Ni alloys, so knowledge of the mechanisms that fractionate C isotopes in such phases is crucial for deciphering the isotopic record of planetary materials. Here we present the results of a diffusion-couple experiment in which cylinders of polycrystalline Fe containing 11,500 and 150μg/g of C were juxtaposed at 1273K and 1.5GPa for a duration of 36min. Diffusion profiles of total C concentration and 13C/12C were measured by secondary ion mass spectrometry (SIMS). The elemental diffusivity extracted from the data is ∼3.0×10−11m2s−1, where 13C/12C was observed to change significantly along the diffusion profile, reflecting a higher diffusivity of 12C relative to 13C. The maximum isotopic fractionation along the diffusion profile is ∼30–40‰. The relative diffusivities (D) of the carbon isotopes can be related to their masses (M) by D13C/D12C=(M12C/M13C)β; the exponent β calculated from our data has a value of 0.225±0.025. Similarly high β values for diffusion of other elements in metals have been taken as an indication of interstitial diffusion, so our results are consistent with C diffusion in Fe by an interstitial mechanism. The high β-value reported here means that significant fractionation of carbon isotopes in nature may arise via diffusion in Fe(–Ni) metal, which is an abundant component of planetary interiors and meteorites.

Discovery of Hg–Cu-bearing metal-sulfide assemblages in a primitive H-3 chondrite: Towards a new insight in early solar system processes

We report here the discovery of a novel meteoritic paragenesis consisting of sub-micrometric HgS, Cu sulfides, and Hg metal, associated with polycrystalline fine-grained native Cu in opaque mineral aggregates heterogeneously distributed in the matrix of the H-3 Tieschitz unequilibrated ordinary chondrite (UOC).The systematic association of Hg with Cu in Tieschitz chondrite provides a unique opportunity to place robust constraints on the origin of these assemblages either by condensation and sulfidation in a local nebular reservoir of non-solar composition, followed by gentle and fast accretion, or by sublimation of Hg from the hot interior of the asteroid and recondensation in its cold outer regions. The sulfide phase relations support low temperature conditions (<300°C), implying that subsequent to accretion indigenous hydrothermal processing, oxidation/sulfidation, transportation, or shock-induced thermal processing of the assemblage on the parent body earlier proposed are very unlikely and unrealistic. Origin of HgS by sublimation of Hg from the hotter asteroid interior and precipitation as cinnabar in the colder surface regions is discrepant with our findings and can be ruled out because cinnabar occurs only in Tieschitz matrix in alternating rhythmic intergrowth with Cu-sulfide. The sublimation scenario calls for co-evaporation of both the highly volatile Hg as HgS and Hg metal and the moderately volatile Cu both as Cu metal, or their sulfides and deposition as sulfides in alternating episodes. Our findings provide further ample evidence refuting the repeated claim of formation of native copper in chondritic metal by shock-induced impact melting. Cold accretion is the only reasonable possibility to preserve the delicate accretionary intergrowth textures, the polycrystallinity of FeNi-metal, native Cu, Hg–Cu-sulfides and native Hg globules and the high Hg concentration retained in this meteorite. Our findings strongly suggest that Tieschitz resided near the cold surface of the parent asteroid.

SARIM PLUS—sample return of comet 67P/CG and of interstellar matter

The Stardust mission returned cometary, interplanetary and (probably) interstellar dust in 2006 to Earth that have been analysed in Earth laboratories worldwide. Results of this mission have changed our view and knowledge on the early solar nebula. The Rosetta mission is on its way to land on comet 67P/Churyumov-Gerasimenko and will investigate for the first time in great detail the comet nucleus and its environment starting in 2014. Additional astronomy and planetary space missions will further contribute to our understanding of dust generation, evolution and destruction in interstellar and interplanetary space and provide constraints on solar system formation and processes that led to the origin of life on Earth. One of these missions, SARIM-PLUS, will provide a unique perspective by measuring interplanetary and interstellar dust with high accuracy and sensitivity in our inner solar system between 1 and 2 AU. SARIM-PLUS employs latest in-situ techniques for a full characterisation of individual micrometeoroids (flux, mass, charge, trajectory, composition) and collects and returns these samples to Earth for a detailed analysis. The opportunity to visit again the target comet of the Rosetta mission 67P/Churyumov-Gerasimeenternko, and to investigate its dusty environment six years after Rosetta with complementary methods is unique and strongly enhances and supports the scientific exploration of this target and the entire Rosetta mission. Launch opportunities are in 2020 with a backup window starting early 2026. The comet encounter occurs in September 2021 and the reentry takes place in early 2024. An encounter speed of 6 km/s ensures comparable results to the Stardust mission.

Whole‐rock 26Al‐26Mg systematics of amoeboid olivine aggregates from the oxidized CV3 carbonaceous chondrite Allende

Abstract– We report on mineralogy, petrography, and whole‐rock 26Al‐26Mg systematics of eight amoeboid olivine aggregates (AOAs) from the oxidized CV chondrite Allende. The AOAs consist of forsteritic olivine, opaque nodules, and variable amounts of Ca,Al‐rich inclusions (CAIs) of different types, and show evidence for alteration to varying degrees. Melilite and anorthite are replaced by nepheline, sodalite, and grossular; spinel is enriched in FeO; opaque nodules are replaced by Fe,Ni‐sulfides, ferroan olivine and Ca,Fe‐rich pyroxenes; forsteritic olivine is enriched in FeO and often overgrown by ferroan olivine. The AOAs are surrounded by fine‐grained, matrix‐like rims composed mainly of ferroan olivine and by a discontinuous layer of Ca,Fe‐rich silicates. These observations indicate that AOAs experienced in situ elemental open‐system iron‐alkali‐halogen metasomatic alteration during which Fe, Na, Cl, and Si were introduced, whereas Ca was removed from AOAs and used to form the Ca,Fe‐rich silicate rims around AOAs. The whole‐rock 26Al‐26Mg systematics of the Allende AOAs plot above the isochron of the whole‐rock Allende CAIs with a slope of (5.23 ± 0.13) × 10−5 reported by Jacobsen et al. (2008). In contrast, whole‐rock 26Al‐26Mg isotope systematics of CAIs and AOAs from the reduced CV chondrite Efremovka define a single isochron with a slope of (5.25± 0.01) × 10−5 (Larsen et al. 2011). We infer that the excesses in 26Mg* present in Allende AOAs are due to their late‐stage open‐system metasomatic alteration. Thus, the 26Al‐26Mg isotope systematics of Allende CAIs and AOAs are disturbed by parent body alteration processes, and may not be suitable for high‐precision chronology of the early solar system events and processes.

On the strong and selective isotope effect in the UV excitation of N 2 with implications toward the nebula and Martian atmosphere

Isotopic effects associated with molecular absorption are discussed with reference to natural phenomena including early solar system processes, Titan and terrestrial atmospheric chemistry, and Martian atmospheric evolution. Quantification of the physicochemical aspects of the excitation and dissociation processes may lead to enhanced understanding of these environments. Here we examine a physical basis for an additional isotope effect during photolysis of molecular nitrogen due to the coupling of valence and Rydberg excited states. The origin of this isotope effect is shown to be the coupling of diabatic electronic states of different bonding nature that occurs after the excitation of these states. This coupling is characteristic of energy regimes where two or more excited states are nearly crossing or osculating. A signature of the resultant isotope effect is a window of rapid variation in the otherwise smooth distribution of oscillator strengths vs. frequency. The reference for the discussion is the numerical solution of the time dependent Schrödinger equation for both the electronic and nuclear modes with the light field included as part of the Hamiltonian. Pumping is to all extreme UV dipole-allowed, valence and Rydberg, excited states of N(2). The computed absorption spectra are convoluted with the solar spectrum to demonstrate the importance of including this isotope effect in planetary, interstellar molecular cloud, and nebular photochemical models. It is suggested that accidental resonance with strong discrete lines in the solar spectrum such as the CIII line at 97.703 nm can also have a marked effect.

O Meteorito Bendegó: história, mineralogia e classificação química

The Bendego meteorite, an iron and nickel mass weighting 5,360 kg, is the largest specimen in the Brazilian collection and holds a rich record of contributions to the meteoritic science. Its finding in 1784 in the hinterland of Bahia State, its epic transportation to the National Museum (Museu Nacional, Rio de Janeiro) in the end of the XIX century, and its participation in the studies which lead to the chemical classification of the metallic meteorites in the 70´s, grant to this space visitor enough credibility to reinforce to the Brazilian geologic community the importance of those extraterrestrial samples, which are authentic records of the beginning of the solar system and early chemical differentiation processes of planets and asteroids. This paper presents new insights regarding the Bendego historic, cosmic, geologic, petrologic and geochemical context and takes advantage from modern analytical methods, such as the instrumental neutron activation analysis, mass inductively coupled plasma spectroscopy, and scanning electronic microscopy, to better characterize the properties of such a Fe-Ni mass which, someday, would be the core of a space object, big enough to experiment a chemical differentiation process.

Simulation of an adsorption solar cooling system

Abstract A more realistic theoretical simulation model for a tubular solar adsorption refrigerating system using activated carbon–methanol (AC/M) pair has been introduced. The mathematical model represents the heat and mass transfer inside the adsorption bed, the condenser, and the evaporator. The simulation technique takes into account the variations of ambient temperature and solar radiation along the day. Furthermore, the local pressure, and local thermal conductivity variations in space and time inside the tubular reactor are investigated as well. A C++ computer program is written to solve the proposed numerical model using the finite difference method. The developed program covers the operations of all the system components along the cycle time. The performance of the tubular reactor, the condenser, and the evaporator has been discussed. Time allocation chart and switching operations for the solar refrigeration system processes are illustrated as well. The case studied has a 1 m2 surface area solar flat plate collector integrated with a 20 stainless steel tubes containing the AC/M pair and each tube has a 5 cm outer diameter. In addition, the condenser pressure is set to 54.2 kpa. It has been found that, the solar coefficient of performance and the specific cooling power of the system are 0.211 and 2.326 respectively. In addition, the pressure distribution inside the adsorption bed has been found nearly uniform and varying only with time. Furthermore, the AC/M thermal conductivity is shown to be constant in both space and time.

Lunar Palaeoregolith Deposits as Recorders of the Galactic Environment of the Solar System and Implications for Astrobiology

One of the principal scientific reasons for wanting to resume in situ exploration of the lunar surface is to gain access to the record it contains of early Solar System history. Part of this record will pertain to the galactic environment of the Solar System, including variations in the cosmic ray flux, energetic galactic events (e.g, supernovae and/or gamma-ray bursts), and passages of the Solar System through dense interstellar clouds. Much of this record is of astrobiological interest as these processes may have affected the evolution of life on Earth, and perhaps other Solar System bodies. We argue that this galactic record, as for that of more local Solar System processes also of astrobiological interest, will be best preserved in ancient, buried regolith ('palaeoregolith') deposits in the lunar near sub-surface. Locating and sampling such deposits will be an important objective of future lunar exploration activities.

Multi-technique investigation reveals new mineral, chemical, and textural heterogeneity in the Tagish Lake C2 chondrite

The Tagish Lake meteorite, an ungrouped C2 chondrite that is related to CI and CM chondrites, is a heterogeneous accretionary breccia with several distinct lithologies that, in bulk, are thought to represent the first known sample of a primitive carbonaceous D-type asteroid. Textural and chemical zoning of clasts and matrix have been little studied and promise additional insight into early solar system processes in both the solar nebula and on the Tagish Lake parent asteroid. We have examined an intact 2.9 g fragment and two polished thin sections from the spring 2000 (non-pristine) Tagish Lake collection to ascertain the major mineralogy and textures of notable features such as chondrules, amoeboid olivine aggregates (AOAs), inclusions, clasts, matrix, and fusion crust. We designed three stages of analysis for this friable meteorite: an initial, non-destructive in situ reconnaissance by μXRD to document meteorite mineralogy and textures and to identify features of interest, followed by spatially correlated μXRD, SEM-EDX and colour SEM-CL analysis of polished thin sections to fully understand mineralogy and the record of texture development, and finally higher resolution SEM-BSE mapping to document smaller scale relationships. Our analyses reveal several previously unreported or poorly characterized features: (1) distinctive colour cathodoluminescence (CL) zoning in relict CAI spinel, in chondrule and AOA forsterite, and in calcite nodules occurring throughout the Tagish Lake matrix. Forsterite frequently shows CL colour and intensity zonation that does not correspond with major or minor element differences resolvable with EPMA, indicating a trace element and/or structural CL-activation mechanism for the zonation that is likely of secondary origin; (2) an irregular inclusion dominated by magnesioaluminate spinel, dolomite, and phyllosilicates with traces of a Ca, Ti oxide phase (likely perovskite) interpreted to be a relict CAI; (3) variable preservation of mesostasis glass in porphyritic olivine chondrules. We anticipate that our multi-technique methodology, particularly non-destructive μXRD, can be successfully applied to other rare and friable materials such as the pristine Tagish Lake fragments.

The thallium isotope composition of carbonaceous chondrites — New evidence for live 205Pb in the early solar system

The extinct radionuclide 205Pb, which decays to 205Tl with a half-life of 15 Ma, is of considerable cosmochemical interest, as it is the only short-lived isotope that is produced exclusively by s-process nucleosynthesis. Evidence for the existence of 205Pb in the early solar system has only recently been obtained from analyses of IAB iron meteorites, but significant uncertainties remain about the initial 205Pb abundance and Tl isotope composition of the solar system. In an attempt to better constrain these values, a comprehensive 205Pb– 205Tl isochron study was carried out on ten carbonaceous chondrites of groups CI, CM, CV, CO and CR. The Pb and Cd isotope compositions of the meteorites were also determined, to correct for terrestrial Pb contamination and eliminate samples that exhibit fractionated Tl isotope compositions from thermal processing. The analyses revealed only limited variation in ε 205Tl, with values of between − 4.0 and + 1.2, but nonetheless the Tl isotope compositions correlate with Pb/Tl ratios. This correlation is unlikely to be due to stable isotope fractionation from terrestrial weathering or early solar system processes, and is most readily explained by in situ decay of 205Pb to 205Tl. Previous 53Mn– 53Cr and 107Pd– 107Ag studies of bulk carbonaceous chondrites provide evidence that the Pb–Tl isochron records volatile fractionation in the solar nebula at close to 4567 Ma. The isochron thus yields the initial 205Pb abundance and Tl isotope composition of the solar system, with values of 205Pb/ 204Pb SS,0 = (1.0 ± 0.4) × 10 − 3 and ε 205Tl SS,0 = − 7.6 ± 2.1, respectively. These results confirm the previous Pb–Tl data for IAB iron meteorites, which provided the first clear evidence for the existence of live 205Pb in the early solar system. The initial 205Pb SS,0 abundance inferred from carbonaceous chondrites demonstrates that the 205Pb– 205Tl decay system is well suited for chronological studies of early solar system processes that produce fractionations in Pb/Tl ratios, including core crystallization and the mobilization of volatiles during thermal processing. The 205Pb SS,0 abundance is close to the upper limit of nucleosynthetic production estimates for AGB stars and thus in accord with contributions of such stars to the early solar system budget of freshly synthesized radioisotopes.

Preservation potential of implanted solar wind volatiles in lunar paleoregolith deposits buried by lava flows

The lunar surface is bathed in a variety of impacting particles originating from the solar wind, solar flares, and galactic cosmic rays. These particles can become embedded in the regolith and/or produce a range of other molecules as they pass through the target material. The Moon therefore contains a record of the variability of the solar and galactic particle fluxes through time. To obtain useful temporal snapshots of these processes, discrete regolith units must be shielded from continued bombardment that would rewrite the record over time. One mechanism for achieving this preservation is the burial of a regolith deposit by a later lava flow. The archival value of such deposits sandwiched between lava layers is enhanced by the fact that both the under- and over-lying lava can be dated by radiometric techniques, thereby precisely defining the age of the regolith layer and the geologic record contained therein. The implanted volatile species would be vulnerable to outgassing by the heat of the over-lying flow, at temperatures exceeding 300–700 °C. However, the insulating properties of the finely particulate regolith would restrict significant heating to shallow depths. We have therefore modeled the heat transfer between lunar mare basalt lavas and the regolith in order to establish the range of depths below which implanted volatiles would be preserved. We find that the full suite of solar wind volatiles, consisting predominantly of H and He, would survive at depths of ∼13–290 cm (for 1–10 m thick lava flows, respectively). A substantial amount of CO, CO 2, N 2 and Xe would be preserved at depths as shallow as 3.7 cm beneath meter-thick flows. Given typical regolith accumulation rates during mare volcanism, the optimal localities for collecting viable solar wind samples would involve stacks of thin mare lava flows emplaced a few tens to a few hundred Ma apart, in order for sufficient regolith to develop between burial events. Obtaining useful archives of Solar System processes would therefore require extraction of regolith deposits buried at quite shallow depths beneath radiometrically-dated mare lava flows. These results provide a basis for possible lunar exploration activities.

Early solar system processes recorded in the matrices of two highly pristine CR3 carbonaceous chondrites, MET 00426 and QUE 99177

The mineralogy and bulk compositions of the matrices of the CR chondrites MET 00426 and QUE 99177 have been studied using a combination of SEM, EPMA, and TEM techniques. The matrices of these two chondrites are texturally, chemically, and mineralogically similar and are characterized by significant FeO-enrichments with respect to other CR chondrite matrices, nearly flat refractory lithophile patterns, variable volatile element patterns, and a simple mineral assemblage dominated by amorphous silicate material and Fe,Ni sulfides. Fine-grained, crystalline silicate phases such as olivine and pyroxene appear to be extremely rare in the matrices of both meteorites. Instead, the mineralogy of matrices and fine-grained rims of both meteorites consists of abundant amorphous FeO-rich silicate material, containing nanoparticles of Fe,Ni sulfides (troilite, pyrrhotite, and pentlandite). Secondary alteration minerals that are characteristic of other CR chondrites (e.g., Renazzo and Al Rais), such as phyllosilicates, magnetite, and calcite are also rare. The texture and mineralogy of the matrices of MET 00426 and QUE 99177 share many features with matrices in the primitive carbonaceous chondrites ALH A77307 (CO3.0) and Acfer 094 (unique). These observations show that MET 00426 and QUE 99177 are very low petrologic type 3 chondrites that have escaped the effects of aqueous alteration, unlike other CR chondrites, which are typically classified as petrologic type 2. We suggest that these meteorites represent additional samples of highly primitive, but extremely rare carbonaceous chondrites of petrologic type 3.00, according to the classification scheme of Grossman and Brearley (2005). The highly pristine nature of MET 00426 and QUE 99177 provides important additional insights into the origins of fine-grained materials in carbonaceous chondrites. Based on our new observations, we infer that the amorphous silicate material and nanosulfide particles that dominate the matrices of these meteorites formed in the solar nebula by rapid condensation of material following high-temperature events, such as those that formed chondrules.