On the original igneous source of Martian fines

The composition of the silicate portion of Martian regolith fines indicates derivation of the fines from mafic to ultramafic igneous rocks, probably rich in pyroxene. Rock types similar in chemical and mineralogical composition include terrestrial Archean basalts and certain achondrite meteorites. If these igneous rocks weathered nearly isochemically, the nontronitic clays proposed earlier as an analog to Martian fines could be formed. Flood basalts of pyroxenitic lavas may be widespread and characteristic of early volcanism on Mars, analogous to maria flood basalts on the Moon and early Precambrian basaltic komatiites on Earth. Compositional differences between lunar, terrestrial, and Martian flood basalts may be related to differences in planetary sizes and mantle compositions of the respective planetary objects.     

Metamorphism in the Martian crust

Compositions of basaltic and ultramafic rocks analyzed by Mars rovers and occurring as Martian meteorites allow predictions of metamorphic mineral assemblages that would form under various thermophysical conditions. Key minerals identified by remote sensing roughly constrain temperatures and pressures in the Martian crust. We use a traditional metamorphic approach (phase diagrams) to assess low‐grade/hydrothermal equilibrium assemblages. Basaltic rocks should produce chlorite + actinolite + albite + silica, accompanied by laumontite, pumpellyite, prehnite, or serpentine/talc. Only prehnite‐bearing assemblages have been spectrally identified on Mars, although laumontite and pumpellyite have spectra similar to other uncharacterized zeolites and phyllosilicates. Ultramafic rocks are predicted to produce serpentine, talc, and magnesite, all of which have been detected spectrally on Mars. Mineral assemblages in both basaltic and ultramafic rocks constrain fluid compositions to be H₂O‐rich and CO₂‐poor. We confirm the hypothesis that low‐grade/hydrothermal metamorphism affected the Noachian crust on Mars, which has been excavated in large craters. We estimate the geothermal gradient (>20 °C km^?1) required to produce the observed assemblages. This gradient is higher than that estimated from radiogenic heat‐producing elements in the crust, suggesting extra heating by regional hydrothermal activity.     

Synthesis of a spinifex‐textured basalt as an analog to Gusev crater basalts,Mars

Abstract– Analyses by the Mars Exploration Rover (MER), Spirit, of Martian basalts from Gusev crater show that they are chemically very different from terrestrial basalts, being characterized in particular by high Mg‐ and Fe‐contents. To provide suitable analog basalts for the International Space Analogue Rockstore (ISAR), a collection of analog rocks and minerals for preparing in situ space missions, especially, the upcoming Mars mission MSL‐2011 and the future international Mars‐2018 mission, it is necessary to synthesize Martian basalts. The aim of this study was therefore to synthesize Martian basalt analogs to the Gusev crater basalts, based on the geochemical data from the MER rover Spirit. We present the results of two experiments, one producing a quench‐cooled basalt (<1 h) and one producing a more slowly cooled basalt (1 day). Pyroxene and olivine textures produced in the more slowly cooled basalt were surprisingly similar to spinifex textures in komatiites, a volcanic rock type very common on the early Earth. These kinds of ultramafic rocks and their associated alteration products may have important astrobiological implications when associated with aqueous environments. Such rocks could provide habitats for chemolithotrophic microorganisms, while the glass and phyllosilicate derivatives can fix organic compounds.     

Altered basaltic glass: A terrestrial analog to the soil of Mars

Analyses of Martian surface soil by Viking and Earth-based telescopes have been interpreted as indicating a regolith dominated by the weathering products of mafic or ultramafic rocks. Basaltic glass has previously been proposed as a more likely precursor than crystalline rock, given the low efficiency of surface weathering under present Martian conditions. On Earth large volumes of basaltic glass formed by quenching of magma by water. A similar interaction, between magma and ground ice, may have been a common occurrence on Mars. On the basis of this scenario palagonite, the alteration product of basaltic sideromelane glass, was studied as a possible analog to Martian soil. Samples from Iceland, Alaska, Antarctica, Hawaii, and the desert of New Mexico and Mexico were examined by optical and scanning electron microscopy, electron microprobe analysis, X-ray diffraction, spectrophotometry, and magnetic and thermogravimetric analysis. We suggest that palagonite is a good analog to the surface soil of Mars in chemical composition, particle size, spectral signature, and magnetic properties. Our model for the formation of fine-grained Martian surface soil begins with eruptions of basaltic magma through ground ice, forming deposits of glassy tuff. Individual glass shards are then altered by low-temperature hydrothermal systems to palagonitic material. Dehydration and aeolian abrasion strip the alteration rinds from the glass, and wind storms distribute the silt-sized palagonitic fragments in a planet-wide deposit.     

A search for basaltic-to-intermediate glasses on Mars: Assessing martian crustal mineralogy

Multiple datasets have demonstrated that the crust of Mars is fundamentally basaltic. However, spectral libraries used to interrogate thermal infrared spectra of Martian dark regions through spectral deconvolution have heretofore lacked mafic glasses despite the importance of amorphous phases (or phases with amorphous-like spectral signatures) in Martian mineralogy. To establish the presence and importance of basaltic-to-intermediate glasses in Martian lithologies, we created five such glasses, obtained their thermal infrared spectra and included the spectra in a library used to deconvolve nine regional Thermal Emission Spectrometer spectra from Mars. We employed the nonnegative least squares (NNLS) deconvolution method, which yields deconvolved phase abundances and the uncertainties associated with those abundances. The basaltic-to-intermediate glasses do not appear in the deconvolution solutions, indicating they are not globally or regionally important phases. Because Martian igneous or impact processes are capable of basaltic-to-intermediate glass formation, the lack of such glasses in the deconvolved mineralogies suggests either the glasses did not form in detectable quantities or they (or their signatures) have been removed. The masking or replacement of basaltic-to-intermediate glasses through alteration is supported by the appearance in the deconvolution solutions of amorphous phases (e.g., silica-rich glasses, opal) or phases with amorphous-like spectral signatures (e.g., clays, zeolites) that commonly form through aqueous alteration of mafic glasses. The glasses may still be important to local-scale thermal infrared studies given the basaltic nature of Mars and the variety of local-scale lithologies detected by various missions. The regional mineralogies derived from the NNLS deconvolution analysis divide into five statistically separable groups, which provide insight into regional trends in mineralogy.     

Nature of the Martian uplands: Effect on Martian meteorite age distribution and secondary cratering

Abstract— Martian meteorites (MMs) have been launched from an estimated 5–9 sites on Mars within the last 20 Myr. Some 80–89% of these launch sites sampled igneous rock formations from only the last 29% of Martian time. We hypothesize that this imbalance arises not merely from poor statistics, but because the launch processes are dominated by two main phenomena: first, much of the older Martian surface is inefficient in launching rocks during impacts, and second, the volumetrically enormous reservoir of original cumulate crust enhances launch probability for 4.5 Gyr old rocks. There are four lines of evidence for the first point, not all of equal strength. First, impact theory implies that MM launch is favored by surface exposures of near‐surface coherent rock (≤10² m deep), whereas Noachian surfaces generally should have ≥10² m of loose or weakly cemented regolith with high ice content, reducing efficiency of rock launch. Second, similarly, both Mars Exploration Rovers found sedimentary strata, 1–2 orders of magnitude weaker than Martian igneous rocks, favoring low launch efficiency among some fluvial‐derived Hesperian and Noachian rocks. Even if launched, such rocks may be unrecognized as meteorites on Earth. Third, statistics of MM formation age versus cosmic‐ray exposure (CRE) age weakly suggest that older surfaces may need larger, deeper craters to launch rocks. Fourth, in direct confirmation, one of us (N. G. B.) has found that older surfaces need larger craters to produce secondary impact crater fields (cf. Barlow and Block 2004). In a survey of 200 craters, the smallest Noachian, Hesperian, and Amazonian craters with prominent fields of secondaries have diameters of ?45 km, ?19 km, and ?10 km, respectively. Because 40% of Mars is Noachian, and 74% is either Noachian or Hesperian, the subsurface geologic characteristics of the older areas probably affect statistics of recognized MMs and production rates of secondary crater populations, and the MM and secondary crater statistics may give us clues to those properties.     

Opal‐A in the Nakhla meteorite: A tracer of ephemeral liquid water in the Amazonian crust of Mars

The nakhlite meteorites are clinopyroxenites that are derived from a ~1300 million year old sill or lava flow on Mars. Most members of the group contain veins of iddingsite whose main component is a fine‐grained and hydrous Fe‐ and Mg‐rich silicate. Siderite is present in the majority of veins, where it straddles or cross‐cuts the Fe‐Mg silicate. This carbonate also contains patches of ferric (oxy)hydroxide. Despite 40 years of investigation, the mineralogy and origins of the Fe‐Mg silicate is poorly understood, as is the paragenesis of the iddingsite veins. Nanometer‐scale analysis of Fe‐Mg silicate in the Nakhla meteorite by electron and X‐ray imaging and spectroscopy reveals that its principal constituents are nanoparticles of opal‐A. This hydrous and amorphous phase precipitated from acidic solutions that had become supersaturated with respect to silica by dissolution of olivine. Each opal‐A nanoparticle is enclosed within a ferrihydrite shell that formed by oxidation of iron that had also been liberated from the olivine. Siderite crystallized subsequently and from solutions that were alkaline and reducing, and replaced both the nanoparticles and olivine. The fluids that formed both the opal‐A/ferrihydrite and the siderite were sourced from one or more reservoirs in contact with the Martian atmosphere. The last event recorded by the veins was alteration of the carbonate to a ferric (oxy)hydroxide that probably took place on Mars, although a terrestrial origin remains possible. These results support findings from orbiter‐ and rover‐based spectroscopy that opaline silica was a common product of aqueous alteration of the Martian crust.     

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.     

K‐Ar dating of rocks on Mars: Requirements from Martian meteorite analyses and isochron modeling

Abstract— Radiometric age dating of Martian rocks and surfaces at known locations for which crater densities can be determined is highly desirable in order to fully understand Martian history. Performing K‐Ar age dating of igneous rocks on Mars by robots, however, presents technical challenges. Some of these challenges can be defined by examining Ar‐Ar data acquired on Martian meteorites, and others can be evaluated through numerical modeling of simulated K‐Ar isochrons like those that would be acquired robotically on Martian rocks. Excess ⁴⁰Ar is present in all shergottites. Thus for Martian rocks, the slopes of K‐Ar isochrons must be determined to reasonable precision in order to calculate reliable ages. Model simulations of possible isochrons give an indication of some requirements in order to define a precise rock age: Issues addressed here are: how many K‐Ar analyses should be made of rocks thought to have the same age; what range of K concentrations should these analyzed samples have; and what analytical uncertainty in K‐Ar measurements is desirable. Meteorite data also are used to determine the D/a² diffusion parameters for Ar in plagioclase and pyroxene separates of several shergottites and nakhlites. These data indicate the required temperatures and times for heating similar Martian rocks in order to extract Ar. Quantitatively extracting radiogenic ⁴⁰Ar could be difficult, and degassing cosmogenic Ar from mafic phases even more so. Considering all these factors, robotic K‐Ar dating of Martian rocks may be achievable, but will be challenging.     

Effect of volatiles and target lithology on the generation and emplacement of impact crater fill and ejecta deposits on Mars

Abstract— Impact cratering is an important geological process on Mars and the nature of Martian impact craters may provide important information as to the volatile content of the Martian crust. Terrestrial impact structures currently provide the only ground‐truth data as to the role of volatiles and an atmosphere on the impact‐cratering process. Recent advancements, based on studies of several well‐preserved terrestrial craters, have been made regarding the role and effect of volatiles on the impact‐cratering process. Combined field and laboratory studies reveal that impact melting is much more common in volatile‐rich targets than previously thought, so impact‐melt rocks, melt‐bearing breccias, and glasses should be common on Mars. Consideration of the terrestrial impact‐cratering record suggests that it is the presence or absence of subsurface volatiles and not the presence of an atmosphere that largely controls ejecta emplacement on Mars. Furthermore, recent studies at the Haughton and Ries impact structures reveal that there are two discrete episodes of ejecta deposition during the formation of complex impact craters that provide a mechanism for generating multiple layers of ejecta. It is apparent that the relative abundance of volatiles in the near‐surface region outside a transient cavity and in the target rocks within the transient cavity play a key role in controlling the amount of fluidization of Martian ejecta deposits. This study shows the value of using terrestrial analogues, in addition to observational data from robotic orbiters and landers, laboratory experiments, and numerical modeling to explore the Martian impact‐cratering record.     

Methane and related trace species on Mars: Origin,loss, implications for life,and habitability

One of the most puzzling aspects of Mars is that organics have not yet been found on the surface. The simplest of organic molecules, methane, was detected in the Martian atmosphere for the first time in 2003. The existence and behavior of methane on Mars is of great significance, as methane is a potential biomarker. In this paper we review our current understanding of possible sources and sinks of methane on Mars. We also investigate the role of other trace species in the maintenance and removal of methane from the atmosphere, as well as of other organic material from the surface. In particular, we examine the exogenous, hydrogeochemical—especially serpentinization—and biological sources, for supplying methane to Mars. We suggest that comets and meteorites are the least likely, whereas low-temperature serpentinization is the most plausible of all candidates to explain the methane observations. Nevertheless, it is premature to rule out the role of biology in producing methane on Mars, in view of available data. It is important to note that the loss of methane to surface must also be factored into any “source” scenarios for methane. Ordinary heterogeneous loss process to surface tends to be very slow. On the other hand, a reactive surface could potentially accelerate the destruction of methane. If correct, it would imply that a larger source of methane is present than currently estimated on the basis of photochemical loss alone. A reactive surface can also explain why no organic material has ever been detected on the Martian surface. The surface could become reactive if some oxidizer were present. We suggest that vast quantities of a powerful oxidant, hydrogen peroxide, can be produced in electrochemistry triggered by electrostatic fields generated in the Martian dust devils and dust storms, and in normal saltation process close to the surface. Finally, current observations are inadequate to prove or disprove the existence of life on Mars, now or in the past. The question of extraterrestrial life is a fundamental one, and it should be addressed meticulously on future missions to Mars. Measurements planned on the Mars Science Laboratory (MSL), especially carbon isotopes and chirality, will go a long way in meeting this goal. A brief overview of the MSL Mission and measurements relevant to the question of life and habitability of Mars is also presented in this paper.     

Moderately and slightly siderophile element constraints on the depth and extent of melting in early Mars

The thermal history of Mars during accretion and differentiation is important for understanding some fundamental aspects of its evolution such as crust formation, mantle geochemistry, chronology, volatile loss and interior degassing, and atmospheric development. In light of data from new Martian meteorites and exploration rovers, we have made a new estimate of Martian mantle siderophile element depletions. New high pressure and temperature metal–silicate experimental partitioning data and expressions are also available. Using these new constraints, we consider the conditions under which the Martian mantle may have equilibrated with metallic liquid. The resulting conditions that best satisfy six siderophile elements—Ni, Co, W, Mo, P, and Ga—and are consistent with the solidus and liquidus of the Martian mantle phase diagram are a pressure of 14 ± 3 GPa and temperature of 2100 ± 200 K. The Martian mantle depletions of Cr and V are also consistent with metal–silicate equilibration in this pressure and temperature range if deep mantle silicate phases are also taken into account. The results are not consistent with either metal–silicate equilibrium at the surface or at the current‐day Martian core–mantle boundary. Recent measurements and modeling have concluded that deep (～17 GPa or 1350 km) mantle melting is required to explain isotopic data for Martian meteorites and the nature of differentiation into core, mantle, and crust. This is in general agreement with our estimates of the conditions of Martian core formation based on siderophile elements that result in an intermediate depth magma ocean scenario for metal–silicate equilibrium.     

Magnetic zones of Mars: Deformation‐controlled origin of magnetic anomalies

Abstract— Intense magnetic anomalies over Martian surface suggest preservation of large volumes of very old crust (>3 Gyr) that formed in the presence of a global magnetic field. The global distribution of the magnetic intensities observed above the Martian crust suggests a division into three zones. Zone 1 is where the magnetic signature is negligible or of relatively low intensity at Mars Global Surveyor (MGS) satellite mapping altitude (400 km). Zone 2 is the region of intermediate crustal magnetic amplitudes and zone 3 is where the highest magnetic intensities are measured. Crater demagnetization near zone 3 reveals the presence of rocks with both high magnetic intensity and coercivity. Magnetic analyses of terrestrial rocks show that compositional banding in orogenic zones significantly enhances both magnetic coercivity and thermal remanent magnetization (TRM) efficiency. Such enhancement offers a novel explanation for the anomalously large intensities inferred of magnetic sources on Mars. We propose that both large magnetic coercivity and intensity near the South Pole is indicative of the presence of a large degree of deformation. Associated compositional zoning creates conditions for large scale magnetic anisotropy allowing magnetic minerals to acquire magnetization more efficiently, thereby causing the distinct magnetic signatures in zone 3, expressed by intense magnetic anomalies. We use a simple model to verify the magnetic enhancement. We hypothesize that magnetically enhanced zone would reside over the down welling plume at the time of magnetization acquisition.     

Alteration minerals,fluids, and gases on early Mars: Predictions from 1‐D flow geochemical modeling of mineral assemblages in meteorite ALH 84001

Clay minerals, although ubiquitous on the ancient terrains of Mars, have not been observed in Martian meteorite Allan Hills (ALH) 84001, which is an orthopyroxenite sample of the early Martian crust with a secondary carbonate assemblage. We used a low‐temperature (20 °C) one‐dimensional (1‐D) transport thermochemical model to investigate the possible aqueous alteration processes that produced the carbonate assemblage of ALH 84001 while avoiding the coprecipitation of clay minerals. We found that the carbonate in ALH 84001 could have been produced in a process, whereby a low‐temperature (~20 °C) fluid, initially equilibrated with the early Martian atmosphere, moved through surficial clay mineral and silica‐rich layers, percolated through the parent rock of the meteorite, and precipitated carbonates (thereby decreasing the partial pressure of CO₂) as it evaporated. This finding requires that before encountering the unweathered orthopyroxenite host of ALH 84001, the fluid permeated rock that became weathered during the process. We were able to predict the composition of the clay minerals formed during weathering, which included the dioctahedral smectite nontronite, kaolinite, and chlorite, all of which have been previously detected on Mars. We also calculated host rock replacement in local equilibrium conditions by the hydrated silicate talc, which is typically considered to be a higher temperature hydrothermal phase on Earth, but may have been a common constituent in the formation of Martian soils through pervasive aqueous alteration. Finally, goethite and magnetite were also found to precipitate in the secondary alteration assemblage, the latter associated with the generation of H₂. Apparently, despite the limited water–rock interaction that must have led to the formation of the carbonates ~ 3.9 Ga ago, in the vicinity of the ALH 84001 source rocks, clay formation would have been widespread.     

Basaltic glass as a habitat for microbial life: Implications for astrobiology and planetary exploration

Recent studies have demonstrated that terrestrial subaqueous basalts and hyaloclastites are suitable microbial habitats. During subaqueous basaltic volcanism, glass is produced by the quenching of basaltic magma upon contact with water. On Earth, microbes rapidly begin colonizing the glassy surfaces along fractures and cracks that have been exposed to water. Microbial colonization of basaltic glass leads to the alteration and modification of the rocks and produces characteristic granular and/or tubular bioalteration textures. Infilling of the alteration textures by minerals such as phyllosilicates, zeolites and titanite may enable their preservation through geologic time. Basaltic rocks are a major component of the Martian crust and are widespread on other solar system bodies. A variety of lines of evidence strongly suggests the long-term existence of abundant liquid water on ancient Mars. Recent orbiter, lander and rover missions have found evidence for the presence of transient liquid water on Mars, perhaps persisting to the present day. Many other solar system bodies, notably Europa, Enceladus and other icy satellites, may contain (or have once hosted) subaqueous basaltic glasses. The record of terrestrial glass bioalteration has been interpreted to extend as far back as ∼3.5 billion years ago and is widespread in oceanic crust and its metamorphic equivalents. The terrestrial record of glass bioalteration strongly suggests that glassy or formerly glassy basaltic rocks on extraterrestrial bodies that have interacted with liquid water are high-value targets for astrobiological exploration.     

Water soluble cations and the fluvial history of mars

The electrical conductivity and water soluble Na, K, Ca, and Mg of aqueous solutions of terrestrial soils and finely divided igneous and metamorphic rocks were determined. Soils from dry terrestrial basins with a history of water accumulation as well as soils from the topographic lows of valleys accumulated water soluble cations, particularly Na and Ca. These soils as a group can be distinguished from the rocks or a second group of soils (leached upland soils and soils from sites other than the topographic lows of valleys) by significant differences in their mean electrical conductivity and water soluble Na + Ca content. Similar measurements on multiple samples from the surface of Mars, collected by an automated long-range roving vehicle along a highlands to basin transect at sites with morphological features resembling dry riverlike channels, are suggested to determine the fluvial history of the planet.     

Evidence for weathering on early Mars from a comparison with terrestrial weathering profiles

Phyllosilicates on Mars are widespread in the ancient crust suggesting the presence of liquid water at the martian surface and therefore warmer conditions during its early history. However, the role of the ancient climate in the alteration process, which produced these phyllosilicates, remains under debate, because similar mineral assemblages can be produced by hydrothermal alteration at depth. This paper focuses on the origin of coincident outcrops of Fe/Mg bearing phyllosilicates and Al-bearing phyllosilicates, which are observed in several regions of Mars. We performed a detailed mineralogical comparison between a section in Nili Fossae, Mars, and a weathering profile located at Murrin Murrin, Western Australia. The Murrin Murrin profile is developed in Archaean serpentinized peridotite massifs over a ∼40 m thick sequence. It has three alteration zones: the serpentine mineral saprolite is found at the bottom, immediately overlain by Fe/Mg-bearing smectites and then Al-bearing phyllosilicates (kaolinite) mixed with iron hydroxides. This example illustrates how Al-dominated minerals can derive from the alteration of initially Al-poor ultramafic rocks by the intense leaching of Mg²⁺. This mineralogical sequence is very similar to that detected locally in Nili Fossae by orbital spectroscopy. By analogy, we propose that the mineral assemblage detected on Mars is the result of long-term weathering, and thus could be the best evidence of past weathering as a direct result of a climate significantly warmer than at present.     

A morphological view on potential niches for exobiology on Mars

The discovery of microbiota in the Dry Valleys of Antarctica has encouraged the construction of new models of Martian ecosystems in order to determine if life could have once existed on Mars. The Antarctic cyanobacteria reside just below the surface of sandstone rocks where they are protected from the extreme cold and dry environment. Analogy with the Antarctic Dry Valleys supports speculation that hypothetical micro-organisms existed on Mars in the early history of the planet and could have migrated into suitable rocks as the availability of liquid water decreased. Although evidence for sandstone layers on Mars has not been substantiated, the palaeohydrology of Martian fluvial valleys (MFVs) reveals the evidence of lake bed sediment depositions which have formed consolidated sediments. As the MFVs formation may result from underground drainage processes, the sediment material would be expected to contain debris such as pumice washload, and pumilith of volcanic and meteoritic origin. These materials may have formed consolidated porous terrains similar to the Antarctic sandstone. Therefore, the endolithic model is consistent with the Martian liquid water habitat model of perenially ice-covered lakes.     

Petrology and shock history of the first depleted-like poikilitic shergottite Asuka 12325

Asuka (A) 12325 is the first poikilitic shergottite having a depleted pattern in light rare earth elements (REE). Compared with known poikilitic shergottites, A 12325 has smaller but more abundant pyroxene oikocrysts with remarkable Fe-rich pigeonite rims, indicating that A 12325 cooled relatively faster at a shallower part of the crust. The redox condition (logfO₂ = IW + 0.6-IW + 1.7) and Fe-rich chemical compositions of each mineral in A 12325 are close to enriched shergottites. The intermediate shergottites could not form by a simple mixing between parent magmas of A 12325 and enriched shergottites. Although A 12325 contains various high-pressure minerals such as majorite and ringwoodite, plagioclase is only partly maskelynitized. Therefore, the maximum shock pressure may be within 17–22 GPa. Thermal conduction and ringwoodite growth calculation around a shock vein revealed that the shock dwell time of A 12325 is at least 40 ms. The weaker shock pressure and longer shock dwell time in A 12325 may be attained by an impact event similar to those of nakhlites and Northwest Africa (NWA) 8159. Such a weak shock ejection event may be as common on Mars as a severe shock event recorded in shergottites. Alteration of sulfide observed in A 12325 may imply the presence of magmatic fluid in its reservoir on Mars. A 12325 expands a chemical variety of Martian rocks and has a unique shock history among poikilitic shergottites while A 12325 also implies that poikilitic shergottites are common rocks on Mars regardless of their sources.     

Shock metamorphism of planetary silicate rocks and sediments: Proposal for an updated classification system

We reevaluate the systematics and geologic setting of terrestrial, lunar, Martian, and asteroidal “impactites” resulting from single or multiple impacts. For impactites derived from silicate rocks and sediments, we propose a unified and updated system of progressive shock metamorphism. “Shock-metamorphosed rocks” occur as lithic clasts or melt particles in proximal impactites at impact craters, and rarely in distal impactites. They represent a wide range of metamorphism, typically ranging from unshocked to shock melted. As the degree of shock metamorphism, at a given shock pressure, depends primarily on the mineralogical composition and the porosity of a rock or sediment sample, different shock classification systems are required for different types of planetary rocks and sediments. We define shock classification systems for eight rock and sediment classes which are assigned to three major groups of rocks and sediments (1) crystalline rocks with classes F, M, A, and U; (2) chondritic rocks (class C); and (3) sedimentary rocks and sediments with classes SR, SE, and RE. The abbreviations stand for felsic (F), mafic (M), anorthositic (A), ultramafic (U), sedimentary rocks (SR), unconsolidated sediments (SE), and regoliths (RE). In each class, the progressive stages of shock metamorphism are denominated S1 to Sx. These progressive shock stages are introduced as: S1–S7 for F , S1–S7 for M, S1–S6 for A , S1–S7 for U , S1–S7 for C , S1–S7 for SR , S1–S5 for SE , and S1–S6 for RE . S1 stands for “unshocked” and Sx (variable between S5 and S7) stands for “whole rock melting.” We propose a sequence of symbols characterizing the degree of shock metamorphism of a sample, i.e., F-S1 to F-S7 with the option to add the tabulated pressure ranges (in GPa) in parentheses.