Hydrogen isotopic composition of the Martian mantle inferred from the newest Martian meteorite fall,Tissint

The hydrogen isotopic composition of planetary reservoirs can provide key constraints on the origin and history of water on planets. The sources of water and the hydrological evolution of Mars may be inferred from the hydrogen isotopic compositions of mineral phases in Martian meteorites, which are currently the only samples of Mars available for Earth‐based laboratory investigations. Previous studies have shown that δD values in minerals in the Martian meteorites span a large range of ?250 to +6000‰. The highest hydrogen isotope ratios likely represent a Martian atmospheric component: either interaction with a reservoir in equilibrium with the Martian atmosphere (such as crustal water), or direct incorporation of the Martian atmosphere due to shock processes. The lowest δD values may represent those of the Martian mantle, but it has also been suggested that these values may represent terrestrial contamination in Martian meteorites. Here we report the hydrogen isotopic compositions and water contents of a variety of phases (merrillites, maskelynites, olivines, and an olivine‐hosted melt inclusion) in Tissint, the latest Martian meteorite fall that was minimally exposed to the terrestrial environment. We compared traditional sample preparation techniques with anhydrous sample preparation methods, to evaluate their effects on hydrogen isotopes, and find that for severely shocked meteorites like Tissint, the traditional sample preparation techniques increase water content and alter the D/H ratios toward more terrestrial‐like values. In the anhydrously prepared Tissint sample, we see a large range of δD values, most likely resulting from a combination of processes including magmatic degassing, secondary alteration by crustal fluids, shock‐related fractionation, and implantation of Martian atmosphere. Based on these data, our best estimate of the δD value for the Martian depleted mantle is ?116 ± 94‰, which is the lowest value measured in a phase in the anhydrously prepared section of Tissint. This value is similar to that of the terrestrial upper mantle, suggesting that water on Mars and Earth was derived from similar sources. The water contents of phases in Tissint are highly variable, and have been affected by secondary processes. Considering the H₂O abundances reported here in the driest phases (most likely representing primary igneous compositions) and appropriate partition coefficients, we estimate the H₂O content of the Tissint parent magma to be ≤0.2 wt%.     

Quantifying noble gas contamination during terrestrial alteration in Martian meteorites from Antarctica

We investigated exterior and interior subsamples from the Martian shergottite meteorites Allan Hills (ALH) A77005 and Roberts Massif (RBT) 04261 for secondary minerals, oxygen isotopes, Ar‐Ar, and noble gas signatures. Electron microprobe investigations revealed that RBT 04261 does not contain any visible alteration even in its most exterior fractures, whereas fracture fillings in ALHA77005 penetrate into the meteorite up to 300 μm, beyond which the fractures are devoid of secondary minerals. Light noble gases seem to be almost unaffected by terrestrially induced alteration in both meteorites. Thus, a shock metamorphic overprint of 30–35 GPa can be deduced from the helium measurements in RBT 04261. Oxygen isotopes also seem unaffected by terrestrially weathering and variations can easily be reconciled with the differences in modal mineralogy of the exterior and interior subsamples. The measurements on irradiated samples (Ar‐Ar) showed a clear Martian atmospheric contribution in ALHA77005, but this is less apparent in our sample of RBT 04261. Exterior and interior subsamples show slight differences in apparent ages, but the overall results are very similar between the two. In contrast, krypton and xenon are severely affected by terrestrial contamination, demonstrating the ubiquitous presence of elementally fractionated air in RBT 04261. Although seemingly contradictory, our results indicate that RBT 04261 was more affected by contamination than ALHA77005. We conclude that irrespective of on which planet the alteration occurred, exposure of Martian rocks to atmosphere (or brine) introduces noble gases with signatures elementally fractionated relative to the respective atmospheric composition into the rock, and relationships of that process with oxygen isotopes or mineralogical observations are not straightforward.     

Terrestrial and Martian weathering signatures of xenon components in shergottite mineral separates

Abstract– Xenon‐isotopic ratios, step‐heating release patterns, and gas concentrations of mineral separates from Martian shergottites Roberts Massif (RBT) 04262, Dar al Gani (DaG) 489, Shergotty, and Elephant Moraine (EET) 79001 lithology B are reported. Concentrations of Martian atmospheric xenon are similar in mineral separates from all meteorites, but more weathered samples contain more terrestrial atmospheric xenon. The distributions of xenon from the Martian and terrestrial atmospheres among minerals in any one sample are similar, suggesting similarities in the processes by which they were acquired. However, in opaque and maskelynite fractions, Martian atmospheric xenon is released at higher temperatures than terrestrial atmospheric xenon. It is suggested that both Martian and terrestrial atmospheric xenon were initially introduced by weathering (low temperature alteration processes). However, the Martian component was redistributed by shock, accounting for its current residence in more retentive sites. The presence or absence of detectable ¹²⁹Xe from the Martian atmosphere in mafic minerals may correspond to the extent of crustal contamination of the rock’s parent melt. Variable contents of excess ¹²⁹Xe contrast with previously reported consistent concentrations of excess ⁴⁰Ar, suggesting distinct sources contributed these gases to the parent magma.     

The provenance,formation, and implications of reduced carbon phases in Martian meteorites

This review is intended to summarize the current observations of reduced carbon in Martian meteorites, differentiating between terrestrial contamination and carbon that is indigenous to Mars. Indeed, the identification of Martian organic matter is among the highest priority targets for robotic spacecraft missions in the next decade, including the Mars Science Laboratory and Mars 2020. Organic carbon compounds are essential building blocks of terrestrial life, so the occurrence and origin (biotic or abiotic) of organic compounds on Mars is of great significance; however, not all forms of reduced carbon are conducive to biological systems. This paper discusses the significance of reduced organic carbon (including methane) in Martian geological and astrobiological systems. Specifically, it summarizes current thinking on the nature, sources, and sinks of Martian organic carbon, a key component to Martian habitability. Based on this compilation, reduced organic carbon on Mars, including detections of methane in the Martian atmosphere, is best described through a combination of abiotic organic synthesis on Mars and infall of extraterrestrial carbonaceous material. Although conclusive signs of Martian life have yet to be revealed, we have developed a strategy for life detection on Mars that can be utilized in future life‐detection studies.     

Gain and loss of uranium by meteorites and rocks,and implications for the redistribution of uranium on Mars

Abstract Terrestrial alteration of meteorites results in the redistribution, gain, or loss of uranium and other elements. We have measured the maximum U adsorption capacity of a meteorite and two geochemical reference materials under conditions resembling terrestrial ones (pH 5.8). The basaltic eucrite Sioux County adsorbs 7 ppm of U. The result for the terrestrial granite AC‐E is similar (5 ppm), while the basalt BE‐N adsorbs 34 ppm of U. We have also investigated U adsorption in the presence of phosphate (0.01 M or less) in imitation of conditions that probably occurred in the earlier history of Mars. Such a process would have alterated Martian surface material and would be noticeable in Martian meteorites from the affected surface. The experiments demonstrated the counteracting effects of phosphate, which increases U adsorption, but decreases the quantity of dissolved U that is available for adsorption. U adsorption by AC‐E increases to 7 ppm. The lowered value for BE‐N of 8 ppm results from the low quantity of dissolved U in the volume of solution used. The results from the adsorption experiments and from leaching the Martian meteorite Zagami and a terrestrial basalt imply that the aqueous redistribution of U on Mars was moderate. Acidic liquids mobilized uranium and other metals, but present phosphate impeded the dissolution of U compounds. Some mobilized U may have reached the global sinks, while most of it probably was transported in the form of suspended particles over a limited distance and then settled.     

New noble gas data of primitive and differentiated achondrites including Northwest Africa 011 and Tafassasset

Abstract— This work reports on the noble gas inventory of 3 new acapulcoites, 3 brachinites, 2 new eucrites from the Dar al Gani region in Libya, the unique achondrite Dar al Gani (DaG) 896 from the same locality, the new eucrite‐like achondrite Northwest Africa (NWA) 011, and the controversial sample Tafassasset. We determined cosmic ray exposure and gas retention ages, evaluated shielding conditions, and discuss the trapped noble gas component of the specimens. All exposure ages are within the known range of stony meteorites and partly confirm previously established age clusters. Shielding conditions vary, suggesting substantial shielding for all 3 brachinites and Tafassasset. We cannot exclude, however, that the Mg‐rich composition of brachinites simply simulates heavy shielding. Regarding the trapped component, we found Q‐like compositions only for the acapulcoite Thiel Mountains (TIL) 99002. The brachinite Elephant Moraine (EET) 99402 yields a high, subsolar ³⁶Ar/¹³²Xe ratio of ?400 along with a slightly elevated ⁸⁴Kr/¹³²atio, indicating minor atmospheric contamination. All the other samples, particularly the eucrite DaG 983, are characterized by clearly elevated Ar/Kr/Xe ratios due to significant terrestrial alteration. Tafassasset exhibits noble gas parameters that are different from those of CR chondrites, including a relatively high cosmic ray exposure age, the absence of a solar component, low ¹³²Xe concentrations, a low trapped ³⁶Ar/¹³²Xe ratio of ?30, and a noticeable amount of radiogenic ¹²⁹Xe. Similar attributes have been observed for some primitive achondrites. These attributes are also consistent with the metamorphic character of the sample. We, therefore, consider Tafassasset's noble gas record to be inconclusive as to its classification (primitive achondrite versus metamorphosed CR chondrite).     

Martian xenon components in Shergotty mineral separates: Locations,sources, and trapping mechanisms

Abstract— Isotopic signatures and concentrations of xenon have been measured in Shergotty mineral separates by laser step heating. Martian atmosphere and ‘martian interior’ xenon are present, as is a spallation component. Martian atmospheric xenon is 5–10 times more concentrated in opaque minerals (magnetite, ilmenite, and pyrrhotite) and maskelynite than in pyroxenes, perhaps reflecting grain size variation. This is shown to be consistent with shock incorporation. A component consisting of solar xenon with a fission contribution, similar to components previously identified in martian meteorites and associated with the martian interior, is best defined in the pyroxene‐dominated separates. This component exhibits a consistent ¹²⁹Xe (¹²⁹Xe/¹³²Xe ?1.2) excess over solar/planetary (¹²⁹Xe/¹³²Xe ?1.04). We suggest that gas present in the melt, perhaps a mixture of interior xenon and martian atmosphere, was incorporated into the pyroxenes in Shergotty as the minerals crystallized.     

A New Martian Meteorite: the Dhofar 019 Shergottite with an Exposure Age of 20 Million Years

The isotopic composition of the noble gases of the new Martian meteorite, the Dhofar 019 shergottite, found in the desert in the territory of the Sultanate of Oman on January 24, 2001, was investigated. Stepwise thermal annealing with isotopic analysis of each of the noble-gas temperature fractions was employed to determine the component composition. The concentration of the trapped noble gases in the new Martian meteorite Dhofar 019 is relatively high, although it lies within the range of concentrations in known SNC meteorites. A characteristic feature of all the trapped noble gases is the presence of two main components: a low-temperature, probably terrestrial atmospheric, component, trapped during the weathering of the meteorite on Earth, and a high-temperature trapped Martian component. Owing to the different ratios of the quantities of the two components, the trapped neon, argon, krypton, and xenon differ markedly in the kinetics of their release. The isotopic composition of the noble gases varies accordingly. The trapped xenon was found to contain two Martian components. One of them, with typical ratios of ¹²⁹Xe/¹³²Xe and ¹³²Xe/⁸⁴Kr, is representative of xenon and krypton of the Martian atmosphere; the other, of gases of the Martian mantle. Variations of the isotopic compositions of helium, neon, and argon (and also, to a lesser extent, of krypton and xenon) during the thermal annealing of the Dhofar 019 meteorite clearly point to a large proportion of cosmogenic as well as trapped components. The concentration of cosmogenic neon and argon in the meteorite is unusually high. This corresponds to a maximum exposure age among other SNC meteorites: 20 million years. Estimates of the potassium–argon age (gas-retention age) yielded the figure of 560 million years, which is within the range of values obtained for SNC meteorites by other authors, who used the rubidium–strontium and the potassium–argon technique.     

Ejection of Martian meteorites

Abstract— We investigated the transfer of meteorites from Mars to Earth with a combined mineralogical and numerical approach. We used quantitative shock pressure barometry and thermodynamic calculations of post‐shock temperatures to constrain the pressure/temperature conditions for the ejection of Martian meteorites. The results show that shock pressures allowing the ejection of Martian meteorites range from 5 to 55 GPa, with corresponding post‐shock temperature elevations of 10 to about 1000 °C. With respect to shock pressures and post‐shock temperatures, an ejection of potentially viable organisms in Martian surface rocks seems possible. A calculation of the cooling time in space for the most highly shocked Martian meteorite Allan Hills (ALH) 77005 was performed and yielded a best‐fit for a post‐shock temperature of 1000 °C and a meteoroid size of 0.4 to 0.6 m. The final burial depths of the sub‐volcanic to volcanic Martian rocks as indicated by textures and mineral compositions of meteorites are in good agreement with the postulated size of the potential source region for Martian meteorites during the impact of a small projectile (200 m), as defined by numerical modeling (Artemieva and Ivanov 2004). A comparison of shock pressures and ejection and terrestrial ages indicates that, on average, highly shocked fragments reach Earth‐crossing orbits faster than weakly shocked fragments. If climatic changes on Mars have a significant influence on the atmospheric pressure, they could account for the increase of recorded ejection events of Martian meteorites in the last 5 Ma.     

Microimaging spectroscopy and scanning electron microscopy of Northwest Africa 8657 shergottite: Interpretation of future in situ Martian data

Microimaging spectroscopy is going to be the new frontier for validating reflectance remote sensed data from missions to solar system bodies. In this field, microimaging spectroscopy of Martian meteorites can provide important and new contributions to interpret data that will be collected by next instruments onboard rover missions to Mars, such as for example Exomars‐2020/Ma_MISS spectrometer. In this paper, a slab from the Northwest Africa (NWA) 8657 shergottite was studied using the SPectral IMager (SPIM) microimaging spectrometer, in the visible‐infrared (VIS‐IR) range, with the aim to subsequently validate the spectral data by means of different independent techniques. The validation was thus carried out, for the first time, comparing SPIM spectral images, characterized by high spatial and spectral resolution, with mineralogical–petrological analyses, obtained by scanning electron microscopy (SEM). The suitability of the SPIM resolution to detect and map augite, pigeonite, maskelynite, and other minor phases as calcite, Ca‐phosphates, and troilite/pyrrhotite with no loss of information about mineral distribution on the slab surface, was ascertained. The good agreement found between spectral and mineralogical data suggests that spectral‐petrography of meteorites may be useful to support in situ investigations on Martian rocks carried out by MaMiss spectrometer during Exomars2020 mission. Moreover, micro spectral images could be also useful to characterize, in a nondestructive way, Martian meteorites and other rare minerals occurring in meteorites. The results obtained in this work represent not only a methodological contribution to the study of meteorites but furnish also elements to reconstruct the history of this sample. The finding of zoned pyroxene, symplectitic texture, amorphous phases as maskelynite, and Fe‐merrillite permits us to hypothesize four stages, i.e., (1) igneous formation of rimmed pyroxenes and other minerals, (2) retrograde metamorphism, (3) shock by impact, and (4) secondary minerals by terrestrial contamination.     

Primordial noble gases in a graphite‐metal inclusion from the Canyon Diablo IAB iron meteorite and their implications

Abstract— We have carried out noble gas measurements on graphite from a large graphite‐metal inclusion in Canyon Diablo. The Ne data of the low‐temperature fractions lie on the mixing line between air and the spallogenic component, but those of high temperatures seem to lie on the mixing line between Ne‐HL and the spallogenic component. The Ar isotope data indicate the presence of Q in addition to air, spallogenic component and Ar‐HL. As the elemental concentration of Ne in Q is low, we could not detect the Ne‐Q from the Ne data. On the other hand, we could not observe Xe‐HL in our Xe data. As the Xe concentration and the Xe/Ne ratio in Q is much higher than that in the HL component, it is likely that only the contribution of Q is observed in the Xe data. Xenon isotopic data can be explained as a mixture of Q, air, and “El Taco Xe.” The Canyon Diablo graphite contains both HL and Q, very much like carbonaceous chondrites, retaining the signatures of various primordial noble gas components. This indicates that the graphite was formed in a primitive nebular environment and was not heated to high, igneous temperatures. Furthermore, a large excess of ¹²⁹Xe was observed, which indicates that the graphite was formed at a very early stage of the solar system when ¹²⁹I was still present. The HL/Q ratios in the graphite in Canyon Diablo are lower than those in carbonaceous chondrites, indicating that some thermal metamorphism occurred on the former. We estimated the temperature of the thermal metamorphism to about 500–600 °C from the difference of thermal retentivities of HL and Q. It is also noted that “El Taco Xe” is commonly observed in many IAB iron meteorites, but its presence in carbonaceous chondrites has not yet been established.     

Martian atmospheric and indigenous components of xenon and nitrogen in the Shergotty,Nakhla, and Chassigny group meteorites

Abstract— In a study of the isotopic signatures of trapped Xe in shock-produced glass of shergottites and in ALH 84001, we observe three components: (1) modern Martian atmospheric Xe that is isotopically mass fractionated relative to solar Xe, favoring the heavy isotopes, (2) solar-like Xe, as previously observed in Chassigny, and (3) an isotopically fractionated (possibly ancient) component with little or no radiogenic ¹²⁹Xe_rad. In situ-produced fission and spallation components are observed predominantly in the high-temperature steps. Heavy N signatures in ALH 84001, EET 79001 and Zagami reveal Martian atmospheric components. The low-temperature release of ALH 84001 shows evidence for the presence of a light N component (δ¹⁵N ≤ -21%), which is consistent with the component observed in the other Shergotty, Nakhla and Chassigny (SNC) group meteorites. The highest observed ¹²⁹Xe/¹³⁰Xe ratio of 15.60 in Zagami and EET 79001 is used here to represent the present Martian atmospheric component, and the isotopic composition of this component is compared with other solar system Xe signatures. The ¹²⁹Xe/¹³⁰Xe ratios in ALH 84001 are lower but appear to reflect varying mixing ratios with other components. The consistently high ¹²⁹Xe/¹³⁰Xe ratios in rocks of different radiometric ages suggest that Martian atmospheric Xe evolved early on. As already concluded in earlier work, only a small fission component is observed in the Martian atmospheric component. Assuming that a chondritic ²⁴⁴Pu/¹²⁹I initial ratio applies to Mars, this implies that either Pu-derived fission Xe is retained in the solid planet (in fact, in situ-produced fission Xe is observed in ALH 84001) or may reflect a very particular degassing history of the planet.     

Hydrous olivine alteration on Mars and Earth

Hydrous alteration of olivine macrocrysts in a Martian olivine phyric basalt, NWA 10416, and a terrestrial basalt from southern Colorado are examined using SEM, EPMA, TEM, and µXRD techniques. The olivines in the meteorite contain linear nanotubes of hydrous material, amorphous areas, and fluid dissolution textures quite distinct from alteration identified in other Martian meteorites. Instead, they bear resemblance to terrestrial deuteric alteration features. The presence of the hydrous alteration phase Mg‐laihunite within the olivines has been confirmed by µXRD analysis. The cores of the olivines in both Martian and terrestrial samples are overgrown by unaltered rims whose compositions match those of a separate population of groundmass olivines, suggesting that the core olivines are xenocrysts whose alteration preceded crystallization of the groundmass. The terrestrial sample is linked to deep crustal metasomatism and the “ignimbrite flare‐up” of the Oligocene epoch. The comparison of the two samples suggests the existence of an analogous relatively water‐rich magmatic reservoir on Mars.     

A search for amino acids and nucleobases in the Martian meteorite Roberts Massif 04262 using liquid chromatography‐mass spectrometry

The investigation into whether Mars contains signatures of past or present life is of great interest to science and society. Amino acids and nucleobases are compounds that are essential for all known life on Earth and are excellent target molecules in the search for potential Martian biomarkers or prebiotic chemistry. Martian meteorites represent the only samples from Mars that can be studied directly in the laboratory on Earth. Here, we analyzed the amino acid and nucleobase content of the shergottite Roberts Massif (RBT) 04262 using liquid chromatography‐mass spectrometry. We did not detect any nucleobases above our detection limit in formic acid extracts; however, we did measure a suite of protein and nonprotein amino acids in hot‐water extracts with high relative abundances of β‐alanine and γ‐amino‐n‐butyric acid. The presence of only low (to absent) levels of several proteinogenic amino acids and a lack of nucleobases suggest that this meteorite fragment is fairly uncontaminated with respect to these common biological compounds. The distribution of straight‐chained amine‐terminal n‐ω‐amino acids in RBT 04262 resembled those previously measured in thermally altered carbonaceous meteorites (Burton et al. 2012; Chan et al. 2012). A carbon isotope ratio of ?24‰ ± 6‰ for β‐alanine in RBT 04262 is in the range of reduced organic carbon previously measured in Martian meteorites (Steele et al. 2012). The presence of n‐ω‐amino acids may be due to a high temperature Fischer‐Tropsch‐type synthesis during igneous processing on Mars or impact ejection of the meteorites from Mars, but more experimental data are needed to support these hypotheses.     

Noble gases in ureilites released by crushing

Abstract— Noble gases in two ureilites, Kenna and Allan Hills (ALH) 78019, were measured with two extraction methods: mechanical crushing in a vacuum and heating. Large amounts of noble gases were released by crushing, up to 26.5% of ¹³²Xe from ALH 78019 relative to the bulk concentration. Isotopic ratios of the crush‐released Ne of ALH 78019 resemble those of the trapped Ne components determined for some ureilites or terrestrial atmosphere, while the crush‐released He and Ne from Kenna are mostly cosmogenic. The crush‐released Xe of ALH 78019 and Kenna is similar in isotopic composition to Q gas, which indicates that the crush‐released noble gases are indigenous and not caused by contamination from terrestrial atmosphere. In contrast to the similarities in isotopic composition with the bulk samples, light elements in the crush‐released noble gases are depleted relative to Xe and distinct from those of each bulk sample. This depletion is prominent especially in the ²⁰Ne/¹³²Xe ratio of ALH 78019 and the ³⁶Ar/¹³²Xe ratio of Kenna. The values of measured ³He/²¹Ne for the gases released by crushing are significantly higher than those for heating‐released gases. This suggests that host phases of the crush‐released gases might be carbonaceous because cosmogenic Ne is produced mainly from elements with a mass number larger than Ne. Based on our optical microscopic observation, tabular‐foliated graphite is the major carbon mineral in ALH 78019, while Kenna contains abundant polycrystalline graphite aggregates and diamonds along with minor foliated graphite. There are many inclusions at the edge and within the interior of olivine grains that are reduced by carbonaceous material. Gaps can be seen at the boundary between carbonaceous material and silicates. Considering these petrologic and noble gas features, we infer that possible host phases of crush‐released noble gases are graphite, inclusions in reduction rims, and gaps between carbonaceous materials and silicates. The elemental ratios of noble gases released by crushing can be explained by fractionation, assuming that the starting noble gas composition is the same as that of amorphous carbon in ALH 78019. The crush‐released noble gases are the minor part of trapped noble gases in ureilites but could be an important clue to the thermal history of the ureilite parent body. Further investigation is needed to identify the host phases of the crush‐released noble gases.     

Understanding the textures and origin of shock melt pockets in Martian meteorites from petrographic studies,comparisons with terrestrial mantle xenoliths,and experimental studies

Abstract— We present a textural comparison of localized shock melt pockets in Martian meteorites and glass pockets in terrestrial, mantle‐derived peridotites. Specific textures such as the development of sieve texture on spinel and pyroxene, and melt migration and reaction with the host rock are identical between these two apparently disparate sample sets. Based on petrographic and compositional observations it is concluded that void collapse/variable shock impedance is able to account for the occurrence of pre‐terrestrial sulfate‐bearing secondary minerals in the melts, high gas emplacement efficiencies, and S, Al, Ca, and Na enrichments and Fe and Mg depletion of shock melt compositions compared to the host rock; previously used as arguments against such a formation mechanism. Recent experimental studies of xenoliths are also reviewed to show how these data further our understanding of texture development and can be used to shed light on the petrogenesis of shock melts in Martian meteorites.     

Helium loss from Martian meteorites mainly induced by shock metamorphism: Evidence from new data and a literature compilation

Abstract— Noble gas data from Martian meteorites have provided key constraints about their origin and evolution, and their parent body. These meteorites have witnessed varying shock metamorphic overprinting (at least 5 to 14 GPa for the nakhlites and up to 45–55 GPa (e.g., the lherzolitic shergottite Allan Hills [ALH] A77005), solar heating, cosmic‐ray exposure, and weathering both on Mars and Earth. Influences on the helium budgets of Martian meteorites were evaluated by using a new data set and literature data. Concentrations of ³He, ⁴He, U, and Th are measured and shock pressures for same sample aliquots of 13 Martian meteorites were determined to asses a possible relationship between shock pressure and helium concentration. Partitioning of ⁴He into cosmogenic and radiogenic components was performed using the lowest ⁴He/³He ratio we measured on mineral separates (⁴He/³He = 4.1, pyroxene of ALHA77005). Our study revealed significant losses of radiogenic ⁴He. Systematics of cosmogenic ³He and neon led to the conclusion that solar radiation heating during transfer from Mars to Earth and terrestrial weathering can be ruled out as major causes of the observed losses of radiogenic helium in bulk meteorites. For bulk rock we observed a correlation of shock pressure and radiogenic ⁴He loss, ranging between ?20% for Chassigny and other moderately shocked Martian meteorites up to total loss for meteorites shocked above 40 GPa. A steep increase of loss occurs around 30 GPa, the pressure at which plagioclase transforms to maskelynite. This correlation suggests significant ⁴He loss induced by shock metamorphism. Noble gas loss in rocks is seen as diffusion due to (1) the temperature increase during shock loading (shock temperature) and (2) the remaining waste heat after adiabatic unloading (post shock temperature). Modeling of ⁴He diffusion in the main U, Th carrier phase apatite showed that post‐shock temperatures of ?300 °C are necessary to explain observed losses. This temperature corresponds to the post‐shock temperature calculated for bulk rocks shocked at about 40 GPa. From our investigation, data survey, and modeling, we conclude that the shock event during launch of the meteorites is the principal cause for ⁴He loss.     

Noble gas record,collisional history,and pairing of CV,CO, CK,and other carbonaceous chondrites

Abstract— Concentration and isotopic composition of the light noble gases as well as of ⁸⁴Kr, ¹²⁹Xe, and ¹³²Xe have been measured in bulk samples of 60 carbonaceous chondrites; 45 were measured for the first time. Solar noble gases were found in nine specimens (Arch, Acfer 094, Dar al Gani 056, Graves Nunataks 95229, Grosnaja, Isna, Mt. Prestrud 95404, Yamato (Y) 86009, and Y 86751). These meteorites are thus regolith breccias. The CV and CO chondrites contain abundant planetary‐type noble gases, but not CK chondrites. Characteristic features of CK chondrites are high ¹²⁹Xe/¹³²Xe ratios. The petrologic type of carbonaceous chondrites is correlated with the concentration of trapped heavy noble gases, similar to observations shown for ordinary chondrites. However, this correlation is disturbed for several meteorites due to a contribution of atmospheric noble gases, an effect correlated to terrestrial weathering effects. Cosmic‐ray exposure ages are calculated from cosmogenic ²¹Ne. They range from about 1 to 63.5 Ma for CO, CV, and CK classes, which is longer than exposure ages reported for CM and CI chondrites. Only the CO3 chondrite Isna has an exceptionally low exposure age of 0.15 Ma. No dominant clusters are observed in the cosmic‐ray exposure age distribution; only for CV and CK chondrites do potential peaks seem to develop at ～9 and ～29 Ma. Several pairings among the chondrites from hot deserts are suggested, but 52 of the 60 investigated meteorites are individual falls. In general, we confirm the results of Mazor et al. (1970) regarding cosmic‐ray exposure and trapped heavy noble gases. With this study, a considerable number of new carbonaceous chondrites were added to the noble gas data base, but this is still not sufficient to obtain a clear picture of the collisional history of the carbonaceous chondrite groups. Obviously, the exposure histories of CI and CM chondrites differ from those of CV, CO, and CK chondrites that have much longer exposure ages. The close relationship among the latter three is also evident from the similar cosmic‐ray exposure age patterns that do not reveal a clear picture of major breakup events. The CK chondrites, however, with their wide range of petrologic types, form the only carbonaceous chondrite group which so far lacks a solar‐gas‐bearing regolith breccia. The CK chondrites contain only minute amounts of trapped noble gases and their noble gas fingerprint is thus distinguishable from the other groups. In the future, more analyses of newly collected CK chondrites are needed to unravel the genetic and historic evolution of this group. It is also evident that the problems of weathering and pairing have to be considered when noble gas data of carbonaceous chondrite are interpreted.     

Noble gases in mineral separates from three shergottites: Shergotty,Zagami, and EETA79001

Abstract— This study provides a complete data set of all five noble gases for bulk samples and mineral separates from three Martian shergottites: Shergotty (bulk, pyroxene, maskelynite), Zagami (bulk, pyroxene, maskelynite), and Elephant Moraine (EET) A79001, lithology A (bulk, pyroxene). We also give a compilation of all noble gas and nitrogen studies performed on these meteorites. Our mean values for cosmic‐ray exposure ages from ³He, ²¹Ne, and ³⁸Ar are 2.48 Myr for Shergotty, 2.73 Myr for Zagami, and 0.65 Myr for EETA79001 lith. A. Serious loss of radiogenic ⁴He due to shock is observed. Cosmogenic neon results for bulk samples from 13 Martian meteorites (new data and literature data) are used in addition to the mineral separates of this study in a new approach to explore evidence of solar cosmic‐ray effects. While a contribution of this low‐energy irradiation is strongly indicated for all of the shergottites, spallation Ne in Chassigny, Allan Hills (ALH) 84001, and the nakhlites is fully explained by galactic cosmic‐ray spallation. Implanted Martian atmospheric gases are present in all mineral separates and the thermal release indicates a near‐surface siting. We derive an estimate for the ⁴⁰Ar/³⁶Ar ratio of the Martian interior component by subtracting from measured Ar in the (K‐poor) pyroxenes the (small) radiogenic component as well as the implanted atmospheric component as indicated from ¹²⁹Xe, * excesses. Unless compromised by the presence of additional components, a high ratio of ～2000 is indicated for Martian interior argon, similar to that in the Martian atmosphere. Since much lower ratios have been inferred for Chassigny and ALH 84001, the result may indicate spatial and/or temporal variations of ⁴⁰Ar/³⁶Ar in the Martian mantle.     

Extinct isotope heterogeneities in the mantles of Earth and Mars: Implications for mantle stirring rates

Heterogeneities in terrestrial samples for ¹⁸²W/¹⁸³W and ¹⁴²Nd/¹⁴⁴Nd are only preserved in Hadean and Archean rocks while heterogeneities in ¹²⁹Xe/¹³⁰Xe and ¹³⁶Xe/¹³⁰Xe persist to very young mantle‐derived rocks. In contrast, meteorites from Mars show that the Martian mantle preserves heterogeneities in ¹⁸²W/¹⁸³W and ¹⁴²Nd/¹⁴⁴Nd up to the present. As a consequence of the probable “deep magma ocean” core formation process, we assume that the Earth and Mars both had a very early two‐mantle‐reservoir structure with different initial extinct nuclide isotopic compositions (different ¹⁸²W/¹⁸³W, ¹⁴²Nd/¹⁴⁴Nd, ¹²⁹Xe/¹³⁰Xe, ¹³⁶Xe/¹³⁰Xe ratios). Based on this assumption, we developed a simple stochastic model to trace the evolution of a mantle with two initially distinct layers for the extinct isotopes and its development into a heterogeneous mantle by convective mixing and stretching of these two layers. Using the extinct isotope system ¹⁸²Hf‐¹⁸²W, we find that the mantles of Earth and Mars exhibit substantially different mixing or stirring rates. This is consistent with Mars having cooled faster than the Earth due to its smaller size, resulting in less efficient mantle mixing for Mars. Moreover, the mantle stirring rate obtained for Earth using ¹⁸²Hf‐¹⁸²W is consistent with the mantle stirring rate of ~500 Myr constrained by the long‐lived isotope system, ⁸⁷Rb‐⁸⁷Sr and ¹⁴⁷Sm‐¹⁴³Nd. The apparent absence of ¹⁸²W/¹⁸³W isotopic heterogeneity in modern terrestrial rocks is attributed to very active mantle stirring which reduced the ¹⁸²W/¹⁸³W isotopic heterogeneity to a relatively small scale (~83 m for a mantle stirring rate of 500 Myr) compared to the common sampling scale of terrestrial basalts (~30 or 100 km). Our results also support the “deep magma ocean” core formation model as being applicable to both Mars and Earth.