The Stardust spacecraft collected thousands of particles from comet 81P/Wild 2 and returned them to Earth for laboratory study. The preliminary examination of these samples shows that the nonvolatile portion of the comet is an unequilibrated assortment of materials that have both presolar and solar system origin. The comet contains an abundance of silicate grains that are much larger than predictions of interstellar grain models, and many of these are high-temperature minerals that appear to have formed in the inner regions of the solar nebula. Their presence in a comet proves that the formation of the solar system included mixing on the grandest scales.

Hydrogen, carbon, nitrogen, and oxygen isotopic compositions are heterogeneous among comet 81P/Wild 2 particle fragments; however, extreme isotopic anomalies are rare, indicating that the comet is not a pristine aggregate of presolar materials. Nonterrestrial nitrogen and neon isotope ratios suggest that indigenous organic matter and highly volatile materials were successfully collected. Except for a single 17 O-enriched circumstellar stardust grain, silicate and oxide minerals have oxygen isotopic compositions consistent with solar system origin. One refractory grain is 16 O-enriched, like refractory inclusions in meteorites, suggesting that Wild 2 contains material formed at high temperature in the inner solar system and transported to the Kuiper belt before comet accretion.

Abstract. The SNC (Shergotty-Nakhla-Chassigny) meteorites have recorded interactions between martian crustal fluids and the parent igneous rocks. The resultant secondary minerals -which comprise up to ~ 1 vol.% of the meteorites -provide information about the timing and nature of hydrous activity and atmospheric processes on Mars. We suggest that the most plausible models for secondary mineral formation involve the evaporation of low temperature o C) brines. This is consistent with the simple mineralogy of these assemblages -Fe-Mg-Ca carbonates, anhydrite, gypsum, halite, clays -and the chemical fractionation of Ca-to Mg-rich carbonate in ALH84001 'rosettes'. Longer-lived, and higher temperature, hydrothermal systems would have caused more silicate alteration than is seen and probably more complex mineral assemblages. Experimental and phase equilibria data on carbonate compositions similar to those present in the SNCs imply low temperatures of formation with cooling taking place over a short period of time (e.g. days). The ALH84001 carbonate also probably shows the effects of partial vapourisation and dehydration related to an impact event postdating the initial precipitation. This shock event may have led to the formation of sulphide and some magnetite in the Fe-rich outer parts of the rosettes.Radiometric dating (K-Ar, Rb-Sr) of the secondary mineral assemblages in one of the nakhlites (Lafayette) suggests that they formed between 0 and 670 Ma, and certainly long after the crystallisation of the host igneous rocks. Crystallisation of ALH84001 carbonate took place 0.5 Ga after the parent rock. These age ranges and the other research on these assemblages suggest that environmental conditions conducive to near-surface liquid water have been present on Mars periodically over the last ~1 Ga. This fluid activity cannot have been continuous over geological time because in that case much more silicate alteration would have taken place in the meteorite parent rocks and the soluble salts would probably not have been preserved.The secondary minerals could have been precipitated from brines with seawater-like composition, high bicarbonate contents and a weakly acidic nature. The co-existence of siderite (Fe-carbonate) and clays in the nakhlites suggests that the pCO 2 level in equilibrium with the parent brine may have been 50 mbar or more. The brines could have originated as flood waters which percolated through the top few hundred metres of the crust, releasing cations from the surrounding parent rocks. There is no spectroscopic or photographic evidence for extensive evaporite deposits on the current martian surface but some salt precipitation through solute concentration must have occurred as floodwaters associated with many of the martian channels ponded in low-lying areas. The high sulphur and chlorine concentrations of the martian soil have most likely resulted from aeolian redistribution of such aqueously-deposited salts and from reaction of the martian surface with volcanic acid volatiles. However, the SNC salt a...

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Abstract-We have measured 0-isotopic ratios in a variety of olivine grains in the C03 chondrite Allan Hills (ALH) A77307 using secondary ion mass spectrometry in order to study the chondrule formation process and the origin of isolated olivine grains in unequilibrated chondrites. Oxygen-isotopic ratios of olivines in this chondrite are variable from B17O = -15.5 to +4.5%0 and B180 = -1 1.5 to +3.9%0, with A170 varying from -10.4 to +3.5%0. Forsteritic olivines, F k l , are enriched in 1 6 0 relative to the bulk chondrite, whereas more FeO-rich olivines are more depleted in 160. Most ratios lie close to the carbonaceous chondrite anhydrous minerals (CCAM) line with negative values of A170, although one grain of composition Fa4 has a mean A170 of + 1.6%0. Marked 0-isotopic heterogeneity within one FeO-rich chondrule is the result of incorporation of relic, 160-rich, Mg-rich grains into a more I60-depleted host. Isolated olivine grains, including isolated forsterites, have similar 0-isotopic ratios to olivine in chondrules of corresponding chemical composition. This is consistent with derivation of isolated olivine from chondrules, as well as the possibility that isolated grains are chondrule precursors. The high 1 6 0 in forsteritic olivine is similar to that observed in forsterite in CV and CI chondrites and the ordinary chondrite Julesburg and suggests nebula-wide processes for the origin of forsterite that appears to be a primitive nebular component.