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Pepin, R. O.

Publications and source records attributed to Pepin, R. O..

At least 19 records

In Situ Measurement of Atmospheric Krypton and Xenon on Mars with Mars Science Laboratory

Mars Science Laboratorys Sample Analysis at Mars (SAM) investigation has measured all of the stable isotopes of the heavy noble gases krypton and xenon in the martian atmosphere, in situ, from the Curiosity Rover at Gale Crater, Mars. Previous knowledge of martian atmospheric krypton and xenon isotope ratios has been based upon a combination of the Viking missions krypton and xenon detections and measurements of noble gas isotope ratios in martian meteorites. However, the meteorite measurements reveal an impure mixture of atmospheric, mantle, and spallation contributions. The xenon and krypton isotopic measurements reported here include the complete set of stable isotopes, unmeasured by Viking. The new results generally agree with Mars meteorite measurements but also provide a unique opportunity to identify various non-atmospheric heavy noble gas components in the meteorites. Kr isotopic measurements define a solar-like atmospheric composition, but deviating from the solar wind pattern at 80Kr and 82Kr in a manner consistent with contributions originating from neutron capture in Br. The Xe measurements suggest an intriguing possibility that isotopes lighter than 132Xe have been enriched to varying degrees by spallation and neutron capture products degassed to the atmosphere from the regolith, and a model is constructed to explore this possibility. Such a spallation component, however, is not apparent in atmospheric Xe trapped in the glassy phases of martian meteorites.

Conrad, P. G.↗

Neon and Helium in the Surface of Stardust Cell C2028

Previous studies of light noble gases in Stardust aerogel samples detected a variety of isotopically non-terrestrial He and Ne compositions. However, with one exception, in none of these samples was there visible evidence for the presence of particles that could have hosted the gases. The exception is materials keystoned from track 41, cell C2044, which contained observable fragments of the impacting Wild 2 comet coma grain. Here we report noble gas data from a second aerogel sample in which grains are observed, cut from the surface of a cell (C2028) riddled with tiny tracks and particles that are thought to be secondary in origin, ejected toward the cell when a parent grain collided with the spacecraft structure and fragmented. Interestingly, measured 20Ne/22Ne ratios in the track 41 and C2028 samples are similar, and within error of the meteoritic "Q-phase" Ne composition.

Palma, R. L.↗

Carbon Raman Spectroscopy of 36 Inter-Planetary Dust Particles

Carbon Raman spectroscopy is a useful tool to determine the degree of order of organic material (OM) in extra-terrestrial matter. As shown for meteoritic OM [e.g., 2], peak parameters of D and G bands are a measure of thermal alteration, causing graphitization (order), and amorphization, e.g. during protoplanetary irradiation, causing disorder. Th e most pristine interplanetary dust particles (IDPs) may come from comets. However, their exact provenance is unknown. IDP collection during Earth?s passage through comet Grigg-Skjellerup?s dust stream ("GSC" collectors) may increase the probability of collecting fresh IDPs from a known, cometary source. We used Raman spectroscopy to compare 21 GSC-IDPs with 15 IDPs collected at different periods, and found that the variation among GSC-IDPs is larger than among non-GSC IDPs, with the most primitive IDPs being mostly GSC-IDPs.

Busemann, H.↗

New Manganese Silicide Mineral Phase in an Interplanetary Dust Particle

Comet 26P/Grigg-Skjellerup was identified as a source of an Earth-crossing dust stream with low Earth-encounter velocities, with peak anticipated fluxes during April in 2003 and 2004 [1]. In response to this prediction, NASA performed dedicated stratospheric dust collections using high altitude aircraft to target potential interplanetary dust particles (IDPs) from this comet stream in April 2003. Several IDPs from this collection have shown unusually low noble gas abundances [2] consistent with the predicted short space exposure ages of Grigg-Skjellerup dust particles [1]. High abundances of large D enrichments [3] and presolar grains [4] in IDPs from this collection are also consistent with an origin from the comet Grigg-Skjellerup. Here we report a new mineral from one of the cluster IDPs of the "Grigg-Skjellerup" collection, L2055. Our report focuses on an unusual manganese-iron-chromium silicide phase that, to our knowledge, has not been observed previously in nature. This unique phase may also shed light on the genesis of the enigmatic low-Fe,Mn-enriched (LIME) olivine that has been previously reported in IDPs and meteorites [5].

Nakamura-Messenger, K.↗

Results of the REFLEX (Return Flux Experiment) Flight Mission

The numerous problems occurring in this first flight of the REFLEX experiment, both in the spacecraft and with the instrument package, seriously constrained the acquisition and analysis of data and severely limited the interpretation of the data that were obtained. Of these, the ambient helium measurements appear to be the most promising. They are summarized and discussed in Appendix A. Further analyses could be attempted to establish the correct values for the energy centers as they varied during the mission. In addition, an extensive laboratory recalibration on a high-speed beam system could in principle provide corrections to be used in analyzing and interpreting the returned data set. The unknown malfunction which generated the energy drift needs to be understood and corrected before the REFLEX experiment is reflown; some hardware modification, or at least retuning, is likely to be required.

Pepin, R. O.↗

Mars atmospheric loss and isotopic fractionation by pick-up-ion sputtering and photochemical escape

We examine the effects of loss of constituents of the Martian atmosphere due to sputtering by solar-wind pick-up ions and photochemical escape during the last 3.8 billion years. Sputtering is capable of efficiently removing species from the upper atmosphere to space, including the light noble gases; nitrogen and oxygen are removed by both sputtering ad photochemical processes. Due to diffusive separation (by mass) above the homopause, removal from the top of the atmosphere will fractionate the isotopes of each species, with the lighter isotope being preferentially lost. This allows current measurements of the isotopic ratios to be used as a measure of the atmospheric evolution as integrated over geologic time. For carbon and oxygen, isotopic fractionation is buffered by exchange of atmospheric species with non-atmospheric reservoirs of CO2 and H2O. This allows us to determine the size of the non-atmospheric reservoirs which are capable of mixing with the atmosphere; these reservoirs can be CO2 absorbed in the regolith and/or H2O in the polar ice caps. Such an exchangeable reservoir is required in order to keep the fractionation of the atmospheric gases as low as is observed.

Jakosky, B. M.↗

Nitrogen and noble gases in a glass sample from LEW88516

The Antarctic meteorite LEW88516 has been classified as a member of the SNC group of meteorites, specifically a shergottite. It is reported to be remarkably similar in mineralogy, petrogenesis and chemistry to the previously known ALH77005 shergottite, with both being compositionally distinct from other shergottites. LEW88516 shows pervasive shock features and has been found to contain glass veins attributable to a shock origin. In an effort to determine whether the glass in LEW88516 contains any of the isotopically-heavy trapped nitrogen component observed in EETA 79001 glass, as well as the related high-Ar-40/Ar-36 and high-Xe-129/Xe-132 components, we undertook an analysis of an 11.9 mg glass sample (LEW88516,4) provided to us by H. Y. McSween, Jr. as part of a consortium study of this meteorite. Nitrogen and noble gases were extracted from LEW88516,4 in a series of combustion steps at increasing temperatures followed by a final pyrolysis. Initial steps at 550 C were intended to remove any surface-sited nitrogen-containing contaminants, while the 700 C step was expected to show the onset of release of a trapped argon component, based on our previous data for EETA 79001. It was hoped that the bulk of any trapped gas release would be concentrated in one of two steps at 1100 C and approximately 1400 C, maximizing our analytical sensitivity. Results of the analysis are shown. Except for He and Ne, data obtained for the 550 C steps will be omitted from further consideration on the assumption that they represent terrestrial contamination.

Becker, R. H.↗

Mars atmosphere loss and isotopic fractionation by solar-wind-induced sputtering and photochemical escape

The effects of loss of Mars atmospheric constituents by solar-wind-induced sputtering and by photochemical escape during the last 3.8 b.y. were examined. Sputtering is capable of efficiently removing all species from the upper atmosphere, including the light noble gases; N also is removed by photochemical processes. Due to the diffusive separation by mass above the homopause, removal from the top of the atmosphere will fractionate the isotopes of each species, with the lighter mass being preferentially lost. For C and O, this allows us to determine the size of nonatmospheric reservoirs that mix with the atmosphere; these reserviors can be accounted for by exchange with CO2 adsorbed in the regolith and with H2O in the polar ice deposits. Both simple analytical models and time-dependent models of the loss of volatiles from and supply to the Martian atmosphere were constructed. Both Ar and Ne require continued replenishment from outgassing over geologic time.

Jakosky, B. M.↗

Evolution of the Martian atmosphere

Evolution of Mars' noble gases through two stages of hydrodynamic escape early in planetary history has been proposed previously by the author. In the first evolutionary stage of this earlier model, beginning at a solar age of approximately 50 m.y., fractionating escape of a H2-rich primordial atmosphere containing CO2, N2, and the noble gases in roughly the proportions found in primitive carbonaceous (CI) chondrites is driven by intense extreme-ultraviolet (EUV) leads to a long (approximately 80 m.y.) period of quiescence, followed by an abrupt degassing of remnant H2, CO2, and N2 from the mantle and of solar-composition noble gases lighter than Xe from the planet's volatile-rich accretional core. Degassed H refuels hydrodynamic loss in a waning but still potent solar EUV flux. Atmospheric Xe, Kr, and Ar remaining at the end of this second escape stage, approximately 4.2 G.y. ago, have evolved to their present-day abundances and compositions. Residual Ne continues to be modified by accretion of solar wind gases throughout the later history of the planet. This model does not address a number of processes that now appear germane to Martian atmospheric history. One, gas loss and fractionation by sputtering, has recently been shown to be relevant. Another, atmospheric erosion, appears increasingly important. In the absence then of a plausible mechanism, the model did not consider the possibility of isotopic evolution of noble gases heavier than Ne after the termination of hydrodynamic escape. Subsequent non-thermal loss of N was assumed, in an unspecified way, to account for the elevation of N from the model value of approximately 250 percent at the end of the second escape stage to approximately 620 percent today. Only qualitative attention was paid to the eroding effects of impact on abundances of all atmophilic species prior to the end of heavy bombardment approximately 3.8 G.y. ago. No attempt was made to include precipitation and recycling of carbonates in tracking the pressure and isotopic history of CO2.

Pepin, R. O.↗

Mars atmospheric loss and isotopic fractionation by solar-wind-induced sputtering and photochemical escape

We examine the effects of loss of Mars atmospheric constituents by solar-wind-induced sputtering and by photochemical escape during the last 3.8 b.y. Sputtering is capable of efficiently removing all species from the upper atmosphere including the light noble gases; N is removed by photochemical processes as well. Due to diffusive separation (by mass) above the homopause, removal from the top of the atmosphere will fractionate the isotopes of each species with the lighter mass being preferentially lost. For C and O, this allows us to determine the size of nonatmospheric reservoirs that mix with the atmosphere; these reservoirs can be CO2 adsorbed in the regolith or H2O in the polar ice caps. We have constructed both simple analytical models and time-dependent models of the loss from and supply of volatiles to the Martian atmosphere.

Jakosky, B. M.↗

A comparison of solar wind and estimated solar system xenon abundances - A test for solid/gas fractionation in the solar nebula

The solar Xe elemental abundance is determined here using solar wind measurements from lunar ilmenites which are normalized to Si by spacecraft data. The results are compared with estimated abundances assuming no fractionation. When corrected for solar wind/photospheric fractionation, the Xe-130 abundance given by surface layer oxidation of ilmenite from solid 71501 exposed within the last 200 m.y. is 0.24 +/- 0.09 normalized to Si = 10 exp 6. This is indistinguishable from estimates made assuming no solid/gas fractionation. Results from breccia 79035 ilmenite exposed at least 1 Gyr ago indicate that the solar wind Xe flux may have been significantly higher relative to other noble gases, perhaps due to more efficient Xe ionization. If this is true, fluxes of C and S, which have first ionization potentials similar to Xe, should also be higher in the ancient solar wind from the same time period.

Wiens, Roger C.↗

Composition of solar wind noble gases released by surface oxidation of a metal separate from the Weston meteorite

The paper reports on a set of experiments intended to test the feasibility of determining elemental and isotopic ratios of the noble gases and nitrogen in the solar wind in metal separates from gas-rich ordinary chondrites. Helium, neon, and argon show clear evidence of a solar wind signature, while no solar component could be identified for xenon and nitrogen. Helium, neon, and argon elemental isotopic ratios appear to depend on depth within the metal grains. The ratios derived indicate that the Weston meteorite did not acquire its solar wind gases from a recent exposure to solar wind, but more probably at a time in the past similar to or even earlier than the exposure time of Apollo 17 breccias. The Ar-36/Ar-38 ratio, in tandem with other recent determinations of this value, indicates that the solar and terrestrial values can no longer be assumed to be equivalent.

Becker, R. H.↗

Solar-wind krypton and solid/gas fractionation in the early solar nebula

The solar-system Kr abundance is calculated from solar-wind noble-gas ratios, determined previously by low-temperature oxidations of lunar ilmenite grains, normalized to Si by spacecraft solar-wind measurements. The estimated Kr-83 abundance of 4.1 + or - 1.5 per million Si atoms is within uncertainty of estimates assuming no fractionation, determined from CI-chondrite abundances of surrounding elements. This is significant because it is the first such constraint on solid/gas fractionation, though the large uncertainty only confines it to somewhat less than a factor of two.

Wiens, Roger C.↗

Long-term changes in composition of solar particles implanted in extraterrestrial materials

Analysis of lunar surface samples for elements implanted therein by solar corpuscular radiation reveals evidence for the following compositional changes over a time period between 1.5 and 3 Gyr: 50-percent decreases in the ratios He-4/Ar-36 and Xe/Ar-36; a 20-percent increase in the ratio He-3/He-4; a 3-percent increase in the ratio Ne-20/Ne-22; and a 50-percent increase in the ratio N-15/N-14. The causes of these changes are not resolved at this time but may include (1) a change in acceleration conditions of the solar wind, (2) a change in flux of solar energetic particles relative to that of the solar wind, and (3) a change in composition of the solar convective zone. There is good evidence for a long-term decrease in the solar-wind flux.

Kerridge, J. F.↗

Laboratory shock emplacement of noble gases, nitrogen, and carbon dioxide into basalt, and implications for trapped gases in shergottite EETA 79001

Basalts from the Servilleta flows, Taos, NM, described by Lofgren (1983) were analyzed by mass spectrometry for shock-implanted noble gases, N2, and CO2 (which were isotopically labeled) after an exposure to 20-60 GPa shock in the presence of 0.0045-3.0 atm of ambient gas. The results were compared with data available on the constituents of the EETA 79001 meteorite. As expected, the samples shocked in this study attained emplacement efficiencies significantly lower than those apparent for lithology C of EETA 79001. Possible explanations for this difference include atmospheric overpressure at the time of EETA 79001 exposure to shock, the trapping of gas already in vugs by the intruding melt material, or the collapse of gas-filled vugs to form gas-laden glass inclusions.

Wiens, R. C.↗

Volatile inventory of Mars-2: Primordial sources and fractionating processes

The total volatile inventory of Mars has been modeled using meteoritic and presumed primordial abundances in the early solar system. Evidence is presented which indicates that the elemental abundances of the noble gases on Earth and Mars are similar, and their ratios are comparable to those in average carbonaceous chondrites with the exception of xenon and krypton. In order to account for presently observed variations in gas abundances, two primordial sources were used. One was the solar composition similar to the solar wind, and the other of carbonaceous grains that were the source for trace exotic components. For Mars, a model in which the early, high solar EUV flux with continued hydrogen production by differentiation results in mass fractionation of the primordial atmosphere, early depletion of xenon, and later depletion of gases lighter than krypton. The result is that the primordial Mars water inventory may have been on the order of 20 to 30 km if spread over the planet.

Pepin, R. O.↗

Nitrogen and light noble gases in Shergotty

Two samples of Shergotty and a sample of EETA 79001's lithology A have been analyzed for N, He, Ne, and Ar abundances and isotopic composition. After correcting for spallogenic nitrogen, the nitrogen isotopic ratios were found to be close to that of the terrestrial atmosphere. The spallogenic noble gas data are consistent with cosmic ray irradiation of both Shergotty and EETA 79001 at shallow shielding depths. Cosmic ray exposure ages were estimated to be in the range of 0.5-0.8 Myr for EETA 79001, and of 2.0-5.2 Myr for Shergotty, depending on the choice of object size and shielding. Among the two Shergotty samples, the contents of Ar-40 differed by a factor of 3. This difference can be attributed to either a small-scale mineralogical inhomogeneity or a significant variation in the degree of degassing of minerals during shock, although the presence of trapped argon with a high Ar-40/Ar-36 ratio and its heterogeneous distribution cannot be ruled out.

Becker, R. H.↗