Energy dissipation at the silica glass/compressed aerogel interface: The fate of Wild 2 mineral grains and fragments smaller than ~100 nm

Allocation FC6,0,10,0,26 from Stardust track 10 shows a slightly wavy silica glass/compressed silica aerogel interface exposing a patchwork of compressed silica aerogel domains and domains of silica glass with embedded Wild 2 materials in ultra‐thin TEM sections. This interface is where molten silica encountered compressed silica aerogel at temperatures <100 °C, and probably near room temperature, causing steep thermal gradients. An Mg, Fe‐olivine grain, and a plagioclase‐leucite intergrowth survived without melting in silica glass. A Mg‐, Al‐, Ca‐, K‐bearing silica globule moved independently as a single object. Two clusters of pure iron, low‐Ni iron, and low‐Ni, low‐sulfur Fe‐Ni‐S grains also survived intact and came to rest right at the interface between silica glass/compressed silica aerogel. There are numerous Fe‐Ni‐S nanograins scattered throughout MgO‐rich magnesiosilica glass, but compositionally similar Fe‐Ni‐S are also found in the compressed silica aerogel, where they are not supposed to be. This work could not establish how deep they had penetrated the aerogel. Iron nanograins in this allocation form core‐ring grains with a gap between the iron core and a surrounding ring of thermally modified aerogel. This structure was caused when rapid, thermal expansion of the core heated the surrounding compressed aerogel that upon rapid cooling remained fixed in place while the iron core shrank back to its original size. The well‐known volume expansion of pure iron allowed reconstruction of the quench temperature for individual core‐ring grains. These temperatures showed the small scale of thermal energy loss at the silica glass/compressed silica aerogel interface. The data support fragmentation of olivine, plagioclase, and iron and Fe ± low‐Ni grains from comet 81P/Wild 2 during hypervelocity capture.     

Fine‐grained material encased in microtracks of Stardust samples

Dust from comet 81P/Wild 2 was captured at high speed in silica aerogel collectors during the Stardust mission. Studies of deceleration tracks in aerogel showed that a number of cometary particles were poorly cohesive and fragmented during impact. Fragments are now scattered along the walls of impact cavities. Here, we report a transmission electron microscope study of a piece of aerogel extracted from the wall of track 10. We focused on micron‐sized secondary tracks along which fragments of a fine‐grained material are disseminated. Two populations of fragments were identified. The first is made of polycrystalline silicate assemblages (olivine, pyroxene, and spinel) that appear to be chemically related to each other. The second corresponds to silica‐rich glassy clumps characteristic of a mixture of melted cometary material and aerogel. A significant number of fragments have been found with a composition close to chondritic CI for the major elements Fe‐Mg‐S at a submicron scale. These fragments have thus never been chemically differentiated by high‐temperature processes prior to the accretion on the comet, in contrast to terminal particles, which are dominated by larger, denser, and frequently monomineralic components.     

Thermal alteration of hydrated minerals during hypervelocity capture to silica aerogel at the flyby speed of Stardust

Abstract— Outside the Earth's atmosphere, silica aerogel is one of the best materials to capture finegrained extraterrestrial particles in impacts at hypervelocities. Because silica aerogel is a superior insulator, captured grains are inevitably influenced by frictional heat. Therefore, we performed laboratory simulations of hypervelocity capture by using light‐gas guns to impact into aerogels finegrained powders of serpentine, cronstedtite, and Murchison CM2 meteorite. The samples were shot at >6 km s^?1 similar to the flyby speed at comet P/Wild‐2 in the Stardust mission. We investigated mineralogical changes of each captured particle by using synchrotron radiation X‐ray diffraction (SR‐XRD), transmission electron microscope (TEM), and field emission scanning electron microscope (FE‐SEM). SR‐XRD of each grain showed that the majority of the bulk grains keep their original mineralogy. In particular, SR‐XRD and TEM investigations clearly exemplified the presence of tochilinite whose decomposition temperature is about 300 °C in the interior of the captured Murchison powder. However, TEM study of these grains also revealed that all the samples experienced melting and vesiculation on the surface. The cronstedtite and the Murchison meteorite powder show remarkable fracturing, disaggregation, melting, and vesiculation. Steep thermal gradients, about 2500 °C/μm were estimated near the surface of the grains (<2 μm thick) by TEM observation. Our data suggests that the interior of >4 μm across residual grains containing abundant materials that inhibit temperature rise would have not experienced >300 °C at the center.     

Stardust glass: Indigenous and modified comet Wild 2 particles

Abstract— Does comet 81P/Wild 2 have indigenous glass? Glass is used here to include all types of amorphous materials that could be either indigenous or modified comet Wild 2 grains, and all amorphous phases in chondritic aggregate interplanetary dust particles (IDPs). The answer is that it probably does, but very little is known of their compositions to allow a definitive answer to be given. There is no evidence among the collected comet dust for interstellar glass with embedded metals and sulfides. There is, however, ample evidence for melting of the smallest, sub‐micrometer comet particles of nanometer‐scale grains similar to those in the matrix of chondritic aggregate IDPs, including pyrrhotite. Massive patches of Mg‐SiO, Al‐SiO, or Ca‐Si‐O glass are incorporated in the familiar, vesicular Si‐rich glass are melted Wild 2 silicates. Magnesiosilica glass has a deep metastable eutectic smectite‐dehydroxylate composition. It indicates that very high temperatures well above the liquidus temperatures of forsterite were achieved very rapidly and were followed but ultra‐rapid quenching. This predictable and systematic response is not limited to Mg‐silicates, and recognizing this phenomenon among massive glass will provide a means to complete the reconstruction of this comet's original minerals, as well as constrain the physiochemical environment created during aerogel melting and evaporation.     

Fine‐grained material of 81P/Wild 2 in interaction with the Stardust aerogel

Abstract– The deceleration tracks in the Stardust aerogel display a wide range of morphologies, which reveal a large diversity of incoming particles from comet 81P/Wild 2. If the large and dense mineral grains survived the extreme conditions of hypervelocity capture, this was not the case for the fine‐grained material that is found strongly damaged within the aerogel. Due to their low mechanical strength, these assemblages were disaggregated, dispersed, and flash melted in the aerogel in walls of bulbous deceleration tracks. Their petrologic and mineralogical properties are found significantly modified by the flash heating of the capture. Originating from a quenched melt mixture of comet material and aerogel, the representative microstructure consists of silica‐rich glassy clumps containing Fe‐Ni‐S inclusions, vesicles and “dust‐rich” patches, the latter being remnants of individual silicate components of the impacting aggregate. The average composition of these melted particle fragments is close to the chondritic CI composition. They might originate from ultrafine‐grained primitive components comparable to those found in chondritic porous IDPs. Capture effects in aerogel and associated sample biases are discussed in terms of size, chemical and mineralogical properties of the grains. These properties are essential for the grain survival in the extremely hot environment of hypervelocity impact capture in aerogel, and thus for inferring the correct properties of Wild 2 material.     

A cometary aggregate interplanetary dust particle as an analog for comet Wild 2 grain chemistry preserved in silica‐rich Stardust glass

Abstract— Many of the nanometer‐scale grains from comet 81P/Wild 2 did not survive hypervelocity capture. Instead, they melted and interacted with silica melt derived from the aerogel used by the Stardust mission. Their petrological properties were completely modified, but their bulk chemistry was preserved in the chemical signatures of mostly vesicular Si‐rich glass with its typical Fe‐Ni‐S compound inclusions. Chondritic aggregate IDP L2011A9 that experienced atmospheric pre‐entry thermal modification was selected as an analog to investigate these Wild 2 chemical signatures. The chemical, petrologic, and mineralogical properties of the individual constituents in this aggregate IDP are presented and used to match the chemical signatures of these Wild 2 grains. Mixing of comet material and pure silica, which is used in a diagram that recognizes this mixing behavior, is used to constrain the probable petrologic and minerals that caused the Wild 2 signatures. The Wild 2 nanometer‐scale grain signatures in Si‐rich glass allocations from three different deceleration tracks resembled mixtures of ultrafine‐grained principal components and dense agglomerate‐like material, Mg‐rich silicates (<500 nm) and Fe,Ni‐sulfides (<100 nm), and Si‐rich amorphous material. Dust resembling the mixed matrix of common chondritic aggregate IDPs was present in Jupiter‐family comet Wild 2.     

Magnetite in Comet Wild 2: Evidence for parent body aqueous alteration

The mineralogy of comet 81P/Wild 2 particles, collected in aerogel by the Stardust mission, has been determined using synchrotron Fe‐K X‐ray absorption spectroscopy with in situ transmission XRD and X‐ray fluorescence, plus complementary microRaman analyses. Our investigation focuses on the terminal grains of eight Stardust tracks: C2112,4,170,0,0; C2045,2,176,0,0; C2045,3,177,0,0; C2045,4,178,0,0; C2065,4,187,0,0; C2098,4,188,0,0; C2119,4,189,0,0; and C2119,5,190,0,0. Three terminal grains have been identified as near pure magnetite Fe₃O₄. The presence of magnetite shows affinities between the Wild 2 mineral assemblage and carbonaceous chondrites, and probably resulted from hydrothermal alteration of the coexisting FeNi and ferromagnesian silicates in the cometary parent body. In order to further explore this hypothesis, powdered material from a CR2 meteorite (NWA 10256) was shot into the aerogel at 6.1 km s^?1, using a light‐gas gun, and keystones were then prepared in the same way as the Stardust keystones. Using similar analysis techniques to the eight Stardust tracks, a CR2 magnetite terminal grain establishes the likelihood of preserving magnetite during capture in silica aerogel.     

Two refractory Wild 2 terminal particles from a carrot‐shaped track characterized combining MIR/FIR/Raman microspectroscopy and FE‐SEM/EDS analyses

We present the analyses results of two bulk Terminal Particles, C2112,7,171,0,0 and C2112,9,171,0,0, derived from the Jupiter‐family comet 81P/Wild 2 returned by the Stardust mission. Each particle embedded in a slab of silica aerogel was pressed in a diamond cell. This preparation, as expected, made it difficult to identify the minerals and organic materials present in these particles. This problem was overcome using a combination of three different analytical techniques, viz. FE‐SEM/EDS, IR, and Raman microspectroscopy that allowed identifying the minerals and small amounts of amorphous carbon present in both particles. TP2 and TP3 were dominated by Ca‐free and low‐Ca, Mg‐rich, Mg,Fe‐olivine. The presence of melilite in both particles is supported by IR microspectroscopy, but is not confirmed by Raman microspectroscopy, possibly because the amounts are too small to be detected. TP2 and TP3 show similar silicate mineral compositions, but Ni‐free and low‐Ni, subsulfur (Fe,Ni)S grains are present in TP2 only. TP2 contains indigenous amorphous carbon hot spots; no indigenous carbon was identified in TP3. These nonchondritic particles probably originated in a differentiated body. This work found an unanticipated carbon contamination following the FE‐SEM/EDS analyses. It is suggested that organic materials in the embedding silica aerogel are irradiated during FE‐SEM/EDS analyses creating a carbon gas that develops a strong fluorescence continuum. The combination of the selected analytical techniques can be used to characterize bulk Wild 2 particles without the need of extraction and removal of the encapsulating aerogel. This approach offers a relatively fast sample preparation procedure, but compressing the samples can cause spurious artifacts, viz. silica contamination. Because of the combination of techniques, we account for these artifacts.     

Organic compound alteration during hypervelocity collection of carbonaceous materials in aerogel

Abstract— The NASA Stardust mission brought to Earth micron‐size particles from the coma of comet 81P/Wild 2 using aerogel, a porous silica material, as the capture medium. A major challenge in understanding the organic inventory of the returned comet dust is identifying, unambiguously, which organic molecules are indigenous to the cometary particles, which are produced from carbon contamination in the Stardust aerogel, and which are cometary organics that have been modified by heating during the particle capture process. Here it is shown that 1) alteration of cometary organic molecules along impact tracks in aerogel is highly dependent on the original particle morphology, and 2) organic molecules on test‐shot terminal particles are mostly preserved. These conclusions are based on two‐step laser mass spectrometry (L²MS) examinations of test shots with organic‐laden particles (both tracks in aerogel and the terminal particles themselves).     

Hypervelocity capture of meteoritic particles in nonsilica aerogels

Abstract– The Stardust mission captured particles from the comet 81P/Wild 2 in gradient density silica aerogel and returned the collected samples to earth in 2006. The analyses of these particles have revealed several new insights into the formation of our solar system. However, since the aerogel used as the capture material was silica, the elemental analyses of the silica‐rich particles were made more complicated in certain ways due to the mixing of the silicon of the particles and that of the aerogel. By using a nonsilica aerogel, future elemental analyses of silica–rich particles captured in aerogel could be made more straightforward. Resorcinol/formaldehyde (RF), alumina, and zirconia aerogels were impact tested with meteoritic fragments and the captured fragments were mapped with synchrotron‐based X‐ray microprobe (XRM) and the particles were analyzed with X‐ray fluorescence (XRF). The resorcinol/formaldehyde aerogel proved to be the best capture material, in that it could be keystoned and XRF could be used to locate and analyze particles that were less than 10 μm.     

Raman spectroscopic investigation of two grains from comet 81P/Wild 2: Information that can be obtained beyond the presence of sp2‐bonded carbon

Abstract– Raman analyses were performed of individual micrometer‐sized fragments of material returned to Earth by the NASA Stardust mission to comet 81P/Wild 2. The studied fragments originated from grains (C2054,0,35,91,0 and C2092,6,80,51,0) of two different penetration tracks that occurred in two different silica aerogel collector cells. All fragments of both particles have Raman spectra characteristic of amorphous sp²‐bonded carbon that are in general agreement with the results published in previous Stardust particle studies. The present study, however, does not focus on the discussion of specific details of the D and G band parameters, but rather reports on additional information that can be obtained from returned Stardust samples via Raman spectroscopy. Most notably, the Raman spectra show that all analyzed fragments of the particles were contaminated with the capture medium (i.e., aerogel). The silica aerogel is laced with organic aliphatic and aromatic hydrocarbon impurities that resulted in strong bands in the ～ 2900 Δcm^?1 spectral range (C‐H stretching modes). Aerogel bands are also found in the 1000–1600 Δcm^?1 spectral range, where they overlap with the bands of the amorphous sp²‐bonded carbon. The peaks associated with the aerogel contamination differ between the two grains that originated from two different aerogel cells. In addition to the bands due to aerogel contamination and the always present sp²‐bonded carbon bands, fragments of particle C2092,6,80,51,0 also show Raman peaks for pyrrhotite and Fa₃₀Fo₇₀ olivine. Complete (up to 4000 Δcm^?1) raw and baseline‐corrected Raman spectra of the Stardust particles are shown and discussed in detail.     

Chemical identification of comet 81P/Wild 2 dust after interacting with molten silica aerogel

Abstract— Flight aerogel in Stardust allocation C2092,2,80,47,6 contains percent level concentrations of Na, Mg, Al, S, Cl, K, Ca, Cr, Mn, Fe, and Ni that have a distinctive Fe‐ and CI‐normalized distribution pattern, which is similar to this pattern for ppb level chemical impurities in pristine aerogel. The elements in this aerogel background were assimilated in non‐vesicular and vesicular glass with the numerous nanometer Fe‐Ni‐S compound inclusions. After correction for the background values, the chemical data show that this piece of comet Wild 2 dust was probably an aggregate of small (<500 nm) amorphous ferromagnesiosilica grains with many tiny Fe,Ni‐sulfide inclusions plus small Ca‐poor pyroxene grains. This distinctive Fe‐ and CI‐normalized element distribution pattern is found in several Stardust allocations. It appears to be a common feature in glasses of quenched aerogel melts but its exact nature is yet to be established.     

Along‐track compositional and textural variation in extensively melted grains returned from comet 81P/Wild 2 by the Stardust mission: Implications for capture‐melting process

Abstract— Five amorphous (extensively melted) grains from Stardust aerogel capture Track 35 were examined by transmission electron microscopy (TEM); two from the bulb, two from near the bulb‐stylus transition, and one from near the terminal particle. Melted grains consist largely of a texturally and compositionally heterogeneous emulsion of immiscible metal/sulfide beads nanometers to tens of nanometers in diameter in a silica‐rich vesicular glass. Most metal/sulfide beads are spherical, but textures of non‐spherical beads indicate that some solidified as large drops during stretching and breaking while in translational and rotational motion, and others solidified from lenses of immiscible liquid at the silicate‐melt/vesicle (vapor) interface. Melted grains appear to become richer in Fe relative to Mg, and depleted in S relative to Fe and Ni with increasing penetration distance along the aerogel capture track. Fe/S ratios are near unity in grains from the bulb of Track 35, consistent with the dominance of Fe‐monosulfide minerals inferred by previous research on Stardust materials. Near‐stoichiometric Fe/S in melted grains from the bulb suggests that Fe‐sulfides in the bulb were dispersed and melted during formation of the bulb but did not lose S. Along‐track increases in Fe/S in melted grains from the bulb through the bulb‐stylus transition and continuing into the stylus indicate that S initially present as iron monosulfide may have been progressively partially volatilized and lost from the melted grains with greater penetration of the grains deeper into the aerogel during capture‐melting of comet dust. Extensively melted grains from the bulbs of aerogel capture tracks may preserve better primary compositional information with less capture‐related modification than grains from farther along the same capture tracks.     

Thermochemical stability of low‐iron,manganese‐enriched olivine in astrophysical environments

Abstract– Low‐iron, manganese‐enriched (LIME) olivine grains are found in cometary samples returned by the Stardust mission from comet 81P/Wild 2. Similar grains are found in primitive meteoritic clasts and unequilibrated meteorite matrix. LIME olivine is thermodynamically stable in a vapor of solar composition at high temperature at total pressures of a millibar to a microbar, but enrichment of solar composition vapor in a dust of chondritic composition causes the FeO/MnO ratio of olivine to increase. The compositions of LIME olivines in primitive materials indicate oxygen fugacities close to those of a very reducing vapor of solar composition. The compositional zoning of LIME olivines in amoeboid olivine aggregates is consistent with equilibration with nebular vapor in the stability field of olivine, without re‐equilibration at lower temperatures. A similar history is likely for LIME olivines found in comet samples and in interplanetary dust particles. LIME olivine is not likely to persist in nebular conditions in which silicate liquids are stable.     

Physical, Chemical, and Mineralogical Properties of Comet 81P/Wild 2 Particles Collected by Stardust

NASA’s Stardust spacecraft collected dust from the coma of Comet 81P/Wild 2 by impact into aerogel capture cells or into Al-foils. The first direct, laboratory measurement of the physical, chemical, and mineralogical properties of cometary dust grains ranging from <10⁻¹⁵ to ∼10⁻⁴ g were made on this dust. Deposition of material along the entry tracks in aerogel and the presence of compound craters in the Al-foils both indicate that many of the Wild 2 particles in the size range sampled by Stardust are weakly bound aggregates of a diverse range of minerals. Mineralogical characterization of fragments extracted from tracks indicates that most tracks were dominated by olivine, low-Ca pyroxene, or Fe-sulfides, although one track was dominated by refractory minerals similar to Ca–Al inclusions in primitive meteorites. Minor mineral phases, including Cu–Fe-sulfide, Fe–Zn-sulfide, carbonate and metal oxides, were found along some tracks. The high degree of variability of the element/Fe ratios for S, Ca, Ti, Cr, Mn, Ni, Cu, Zn, and Ga among the 23 tracks from aerogel capture cells analyzed during Stardust Preliminary Examination is consistent with the mineralogical variability. This indicates Wild 2 particles have widely varying compositions at the largest size analyzed (>10 μm). Because Stardust collected particles from several jets, sampling material from different regions of the interior of Wild 2, these particles are expected to be representative of the non-volatile component of the comet over the size range sampled. Thus, the stream of particles associated with Comet Wild 2 contains individual grains of diverse elemental and mineralogical compositions, some rich in Fe and S, some in Mg, and others in Ca and Al. The mean refractory element abundance pattern in the Wild 2 particles that were examined is consistent with the CI meteorite pattern for Mg, Si, Cr, Fe, and Ni to 35%, and for Ca, Ti and Mn to 60%, but S/Si and Fe/Si both show a statistically significant depletion from the CI values and the moderately volatile elements Cu, Zn, Ga are enriched relative to CI. This elemental abundance pattern is similar to that in anhydrous, porous interplanetary dust particles (IDPs), suggesting that, if Wild 2 dust preserves the original composition of the Solar Nebula, the anhydrous, porous IDPs, not the CI meteorites, may best reflect the Solar Nebula abundances. This might be tested by elemental composition measurements on cometary meteors.     

Kosmochloric Ca‐rich pyroxenes and FeO‐rich olivines (Kool grains) and associated phases in Stardust tracks and chondritic porous interplanetary dust particles: Possible precursors to FeO‐rich type II chondrules in ordinary chondrites

Abstract— Terminal particles and mineral fragments from comet 81P/Wild 2 were studied in 16 aerogel tracks by transmission and secondary electron microscopy. In eight tracks clinopyroxenes with correlated Na₂O and Cr₂O₃ contents as high as 6.0 wt% and 13.0 wt%, respectively, were found. Kosmochloric (Ko) clinopyroxenes were also observed in 4 chondritic interplanetary dust particles (IDPs). The Ko‐clinopyroxenes were often associated with FeO‐rich olivine ± Cr‐rich spinel ± aluminosilicate glass or albitic feldspar, assemblages referred to as Kool grains (Ko = kosmochloric Ca‐rich pyroxene, ol = olivine). Fine‐grained (submicron) Kool fragments have textures suggestive of crystallization from melts while coarse‐grained (>1 μm) Kool fragments are often glass‐free and may have formed by thermal metamorphism in the nebula. Average major and minor element distributions between clinopyroxenes and coexisting FeO‐rich olivines are consistent with these phases forming at or near equilibrium. In glass‐bearing fine‐grained Kool fragments, high concentrations of Na in the clinopyroxenes are inconsistent with existing experimentally determined partition coefficients at equilibrium. We speculate that the availability of Cr in the melt increased the clinopyroxene Na partition coefficient via a coupled substitution thereby enhancing this phase with the kosmochlor component. The high temperature minerals, fine‐grain sizes, bulk compositions and common occurrence in the SD tracks and IDPs support the idea that Kool grains could have been precursors to type II chondrules in ordinary chondrites. These grains, however, have not been observed in these meteorites suggesting that they were destroyed during chondrule formation and recycling or were not present in the nebula at the time and location where meteoritic chondrules formed.     

Non‐silica aerogels as hypervelocity particle capture materials

Abstract– The Stardust sample return mission to the comet Wild 2 used silica aerogel as the principal cometary and interstellar particle capture and return medium. However, since both cometary dust and interstellar grains are composed largely of silica, using a silica collector complicates the science that can be accomplished with these particles. The use of non‐silica aerogel in future extra‐terrestrial particle capture and return missions would expand the scientific value of these missions. Alumina, titania, germania, zirconia, tin oxide, and resorcinol/formaldehyde aerogels were produced and impact tested with 20, 50, and 100 μm glass microspheres to determine the suitability of different non‐silica aerogels as hypervelocity particle capture mediums. It was found that non‐silica aerogels do perform as efficient hypervelocity capture mediums, with alumina, zirconia, and resorcinol/formaldehyde aerogels proving to be the best of the materials tested.     

Investigation of iron sulfide impact crater residues: A combined analysis by scanning and transmission electron microscopy

Abstract– Samples returned from comet 81P/Wild 2 by the Stardust mission provided an unequaled opportunity to compare previously available extraterrestrial samples against those from a known comet. Iron sulfides are a major constituent of cometary grains commonly identified within cometary interplanetary dust particles (IDPs) and Wild 2 samples. Chemical analyses indicate Wild 2 sulfides are fundamentally different from those in IDPs. However, as Wild 2 dust was collected via impact into capture media at approximately 6.1 km s^?1, it is unclear whether this is due to variation in preaccretional/parent body processes experienced by these materials or due to heating and alteration during collection. We investigated alteration in pyrrhotite and pentlandite impacted into Stardust flight spare Al foils under encounter conditions by comparing scanning and transmission electron microscope (SEM, TEM) analyses of preimpact and postimpact samples and calculating estimates of various impact parameters. SEM is the primary method of analysis during initial in situ examination of Stardust foils, and therefore, we also sought to evaluate the data obtained by SEM using insights provided by TEM. We find iron sulfides experience heating, melting, separation, and loss of S, and mixing with molten Al. These results are consistent with estimated peak pressures and temperatures experienced (approximately 85 GPa, approximately 2600 K) and relative melting temperatures. Unambiguous identification of preserved iron sulfides may be possible by TEM through the location of Al‐free regions. In most cases, the Ni:Fe ratio is preserved in both SEM and TEM analyses and may therefore also be used to predict original chemistry and estimate mineralogy.     

Complex aromatic hydrocarbons in Stardust samples collected from comet 81P/Wild 2

Abstract– The successful return of the Stardust spacecraft provides a unique opportunity to investigate the nature and distribution of organic matter in cometary dust particles collected from comet 81P/Wild 2. Analysis of individual cometary impact tracks in silica aerogel using the technique of two‐step laser mass spectrometry demonstrates the presence of complex aromatic organic matter. While concerns remain as to the organic purity of the aerogel collection medium and the thermal effects associated with hypervelocity capture, the majority of the observed organic species appear indigenous to the impacting particles and are hence of cometary origin. While the aromatic fraction of the total organic matter present is believed to be small, it is notable in that it appears to be N rich. Spectral analysis in combination with instrumental detection sensitivies suggest that N is incorporated predominantly in the form of aromatic nitriles (R–C≡N). While organic species in the Stardust samples do share some similarities with those present in the matrices of carbonaceous chondrites, the closest match is found with stratospherically collected interplanetary dust particles. These findings are consistent with the notion that a fraction of interplanetary dust is of cometary origin. The presence of complex organic N containing species in comets has astrobiological implications as comets are likely to have contributed to the prebiotic chemical inventory of both the Earth and Mars.     

GEMS,hydrated chondritic IDPs,CI‐matrix material: Sources of water in 81P/comet Wild 2

So far there is no conclusive evidence for water in the nucleus of 81P/comet Wild 2. Recently magnetite in collected Wild 2 samples was cited as proxy evidence for parent body aqueous alteration in this comet (Hicks et al. 2017 ). A potentional source for water of hydration would be layer silicates but unfortunately there is no record, neither texturally nor chemically, for hydrated layer silicates that survived hypervelocity impact in the Wild 2 samples. This paper reports large vesicles in the matrix of allocation C2044,2,41,2,5 from a volatile‐rich type B/C Stardust track. These vesicles were probably caused by boiling water that were generated when hydrated Wild 2 silicates impacted the near‐surface silica aerogel layer. Potential water sources were partially and fully hydrated GEMS (glass with embedded metal and sulfides) and CI carbonaceous chondrite materials among the earliest dusts that experienced hydration and icy‐body formation and long‐range transport and mixing with materials from across the solar system.