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.     

Amino acid photostability on the Martian surface

Abstract— In the framework of international planetary exploration programs, several space missions are planned to search for organics and bio‐signatures on Mars. Previous attempts have not detected any organic compounds in the Martian regolith. It is therefore critical to investigate the processes that may affect organic molecules on and below the planet's surface. Laboratory simulations can provide useful data about the reaction pathways of organic material at Mars' surface. We have studied the stability of amino acid thin films against ultraviolet (UV) irradiation and use those data to predict the survival time of these compounds on and in the Martian regolith. We show that thin films of glycine and D‐alanine are expected to have half‐lives of 22 ± 5 hr and of 3 ± 1 hr, respectively, when irradiated with Mars‐like UV flux levels. Modelling shows that the half‐lives of the amino acids are extended to the order of 10⁷ years when embedded in regolith. These data suggest that subsurface sampling must be a key component of future missions to Mars dedicated to organic detection.     

The effects of Martian near surface conditions on the photochemistry of amino acids

In order to understand the complex multi-parameter system of destruction of organic material on the surface of Mars, step-by-step laboratory simulations of processes occurring on the surface of Mars are necessary. This paper describes the measured effects of two parameters, a CO₂ atmosphere and low temperature, on the destruction rate of amino acids when irradiated with Mars-like ultraviolet light (UV). The results show that the presence of a 7 mbar CO₂ atmosphere does not affect the destruction rate of glycine, and that cooling the sample to 210 K (average Mars temperature) lowers the destruction rate by a factor of 7. The decrease in the destruction rate of glycine by cooling the sample is thought to be predominantly caused by the slower reaction kinetics. When these results are scaled to Martian lighting conditions, cold thin films of glycine are assumed to have half-lives of 250 h under noontime peak illumination. It has been hypothesised that the absence of detectable native organic material in the Martian regolith points to the presence of oxidising agents. Some of these agents might form via the interaction of UV with compounds in the atmosphere. Water, although a trace component of Mars’ atmosphere, is suggested to be a significant source of oxidising species. However, gaseous CO₂ or adsorbed H₂O layers do not influence the photodestruction of amino acids significantly in the absence of reactive soil. Other mechanisms such as chemical processes in the Martian regolith need to be effective for rapid organic destruction.     

Drilling in ancient permafrost on Mars for evidence of a second genesis of life

If life ever existed on Mars, a key question is the genetic relationship of that life to life on Earth. To determine if Martian life represents a separate, second genesis of life requires the analysis of organisms, not fossils. Ancient permafrost on Mars represents one potential source of intact, albeit probably dead by radiation, Martian organisms. Strong crustal magnetism in the ancient heavily cratered southern highlands between 60 and 80°S and at about 180°W indicates what may be the oldest, best preserved ice-rich permafrost on Mars. Drilling to depths of 1000 m would reach samples unaffected by possible warming due to cyclic changes in Mars’ obliquity. When drilling into the permafrost to retrieve ancient intact Martian organisms, it is necessary to take special precautions to avoid the possibility of contamination. Earth permafrost provides an analog for Martian permafrost and convenient sites for instrument development and field testing.     

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.     

Assessment of Raman spectroscopy as a tool for the non-destructive identification of organic minerals and biomolecules for Mars studies

Several characteristic geological features found on the surface of Mars by planetary rovers suggest that a possible extinct biosphere could exist based on similar sources of energy as occurred on Earth. For this reason, analytical instrumental protocols for the detection of biomarkers in suitable geological matrices unequivocally have to be elaborated for future unmanned explorations including the forthcoming ESA ExoMars mission. As part of the Pasteur suite of analytical instrumentation on ExoMars, the Raman/LIBS instrument will seek elemental and molecular information about geological, biological and biogeological markers in the Martian record. A key series of experiments on terrestrial Mars analogues, of which this paper addresses a particularly important series of compounds, is required to obtain the Raman spectra of key molecules and crystals, which are characteristic for each biomarker. Here, we present Raman spectra of several examples of organic compounds which have been recorded non-destructively—higher n-alkanes, polycyclic aromatic hydrocarbons, carotenoids, salts of organic acids, pure crystalline terpenes as well as oxygen-containing organic compounds. In addition, the lower limit of β-carotene detection in sulphate matrices using Raman microspectroscopy was estimated.     

NanoSIMS analysis of organic carbon from the Tissint Martian meteorite: Evidence for the past existence of subsurface organic‐bearing fluids on Mars

Two petrographic settings of carbonaceous components, mainly filling open fractures and occasionally enclosed in shock‐melt veins, were found in the recently fallen Tissint Martian meteorite. The presence in shock‐melt veins and the deuterium enrichments (δD up to +1183‰) of these components clearly indicate a pristine Martian origin. The carbonaceous components are kerogen‐like, based on micro‐Raman spectra and multielemental ratios, and were probably deposited from fluids in shock‐induced fractures in the parent rock of Tissint. After precipitation of the organic matter, the rock experienced another severe shock event, producing the melt veins that encapsulated a part of the organic matter. The C isotopic compositions of the organic matter (δ¹³C = ?12.8 to ?33.1‰) are significantly lighter than Martian atmospheric CO₂ and carbonate, providing a tantalizing hint for a possible biotic process. Alternatively, the organic matter could be derived from carbonaceous chondrites, as insoluble organic matter from the latter has similar chemical and isotopic compositions. The presence of organic‐rich fluids that infiltrated rocks near the surface of Mars has significant implications for the study of Martian paleoenvironment and perhaps to search for possible ancient biological activities on Mars.     

Microbial life in martian ice: A biotic origin of methane on Mars?

Despite the fact that microbial cells are unlikely to be found in the Martian soil in the near future, this paper is written on the assumption that some of the seasonally varying concentration of Martian methane is due to ongoing methanogenesis. It is first pointed out that life might have arisen on Mars first and been transported to Earth later. A case is made that an icy origin of life is more likely than a hot origin, especially if biomolecules take advantage of the high encounter rates and stability against hydrolysis, and that microorganisms feed on the ions that comprise eutectic solutions in ice. Although certain difficulties are avoided if RNA and DNA grow while adsorbed on clay grains, double strand-breaks of microbial DNA due to alpha radioactivity are a far greater threat to microbial survival on clay or other rock types than in ice. Developing a relation between the rate of microbial metabolism in ice and the experimentally determined rate of production of trapped gases of microbial origin, one can estimate the concentration of methanogens that could account for the methane production rate as a function of temperature of their habitat. The result, of order 1 cell cm⁻³ in the Martian subsurface, seems an attainable goal provided samples are taken from at least 1 or 2 m below the hostile surface of Mars. Instruments on NASA’s 2011 Mars Science Lab will measure stable isotopes for methane, water, and carbon dioxide, which on Earth served to distinguish abiotic, thermogenic, and microbial origins. Future measurements of chirality of biomolecules might also provide evidence for Martian life.     

History of Martian volatiles: Implications for organic synthesis

A theoretical reconstruction of the history of Martian volatiles indicates that Mars probably possessed a substantial reducing atmosphere at the outset of its history and that its present tenous and more oxidized atmosphere is the result of extensive chemical evolution. As a consequence, it is probable that Martian atmospheric chemical conditions, now hostile with respect to abiotic organic synthesis in the gas phase, were initially favorable. Evidence indicating the chronology and degradational history of Martian surface features, surface mineralogy, bulk volatile content, internal mass distribution, and thermal history suggests that Mars catastrophically developed a substantial reducing atmosphere as the result of rapid accretion. This atmosphere probably persisted—despite the direct and indirect effects of hydrogen escape—for a geologically short time interval during, and immediately following, Martian accretion. That was the only portion of Martian history when the atmospheric environment could have been chemically suited for organic synthesis in the gas phase. Subsequent gradual degrassing of the Martian interior throughout Martian history could not sustain a reducing atmosphere due to the low intensity of planet-wide orogenic activity and the short atmospheric mean residence time of hydrogen on Mars. During the post-accretion history of Mars, the combined effects of planetary hydrogen escape, solar-wind sweeping, and reincorporation of volatiles into the Martian surface produced and maintained the present atmosphere.     

Response of the intermediate complexity Mars Climate Simulator to different obliquity angles

A climate model of intermediate complexity, named the Mars Climate Simulator, has been developed based on the Portable University Model of the Atmosphere (PUMA). The main goal of this new development is to simulate the climate variations on Mars resulting from the changes in orbital parameters and their impact on the layered polar terrains (also known as permanent polar ice caps). As a first step towards transient simulations over several obliquity cycles, the model is applied to simulate the dynamical and thermodynamical response of the Martian climate system to different but fixed obliquity angles. The model is forced by the annual and daily cycle of solar insolation. Experiments have been performed for obliquities of φ=15^° (minimum), φ=25.2^° (present), and φ=35^° (maximum). The resulting changes in solar insolation mainly in the polar regions impact strongly on the cross-equatorial circulation which is driven by the meridional temperature gradient and steered by the Martian topography. At high obliquity, the cross-equatorial near surface flow from the winter to the summer hemisphere is strongly enhanced compared to low obliquity periods. The summer ground temperature ranges from 200 K (φ=15^°) to 250 K (φ=35^°) at 80^°N in northern summer, and from 220 K (φ=15^°) to 270 K (φ=35^°) at 80^°S in southern summer. In the atmosphere at 1 km above ground, the respective range is 195-225 K in northern summer, and 210-250 K in southern summer.     

Beta-carotene—A possible biomarker in the Martian evaporitic environment: Raman micro-spectroscopic study

Due to the discovery of the evaporitic environment on the Martian surface, there is a reasonable possibility that evaporites served (or still serve) as habitats for microbial life if ever present on Mars. At the very least, if no signatures of extant life exist within these rocks, it may sustain molecular remnants as evidence for living organisms in the past. β-Carotene, among other carotenoids, could be such a suitable biomarker. In this study, Raman micro-spectroscopy was tested as a nondestructive method of determining the presence of β-carotene in experimentally prepared evaporitic matrices. Samples prepared by mixing β-carotene with powdered gypsum (CaSO₄·2H₂O), halite (NaCl) and epsomite (MgSO₄·7H₂O) were analyzed using a 785 nm excitation source. Various concentrations of β-carotene in the matrices were investigated to determine the lowest β-carotene content detectable by Raman micro-spectroscopy. Mixtures were also measured with a laser beam permeating the crystals of gypsum and epsomite in order to evaluate the possibility of identifying β-carotene inside the mineral matrix.We were able to obtain a clear β-carotene signal at the 10 mg kg⁻¹ concentration level—the number of registered β-carotene Raman bands differed depending on the particular mineral matrix. Spectral signatures of β-carotene were detected even when analyzing samples containing 1 mg kg⁻¹ of this molecule. The 10-100 mg kg⁻¹ of β-carotene in mineral matrices (halite, epsomite) was detected when analyzed through the monocrystal of gypsum and epsomite, respectively. These results will aid both in-situ analyses on Mars and sample analyses on Earth.     

Could organic matter have been preserved on Mars for 3.5 billion years?

3.5 billion years (byr) ago, when it is thought that Mars and Earth had similar climates, biological evolution on Earth had made considerable progress, such that life was abundant. It is therefore surmised that prior to this time period the advent of chemical evolution and subsequent origin of life occurred on Earth and may have occurred on Mars. Analysis for organic compounds in the soil buried beneath the Martian surface may yield useful information regarding the occurrence of chemical evolution and possibly biological evolution. Calculations based on the stability of amino acids lead to the conclusion that remnants of these compounds, if they existed on Mars 3.5 byr ago, might have been preserved buried beneath the surface oxidizing layer. For example, if phenylalanine, an amino acid of average stability, existed on Mars 3.5 byr ago, then 1.6% would remain buried today, or 25 pg-2.5 ng of C g-1 Martian soil may exist from remnants of meteoritic and cometary bombardment, assuming that 1% of the organics survived impact.     

Experimental determination of photostability and fluorescence‐based detection of PAHs on the Martian surface

Abstract– Even in the absence of any biosphere on Mars, organic molecules, including polycyclic aromatic hydrocarbons (PAHs), are expected on its surface due to delivery by comets and meteorites of extraterrestrial organics synthesized by astrochemistry, or perhaps in situ synthesis in ancient prebiotic chemistry. Any organic compounds exposed to the unfiltered solar ultraviolet spectrum or oxidizing surface conditions would have been readily destroyed, but discoverable caches of Martian organics may remain shielded in the subsurface or within surface rocks. We have studied the stability of three representative polycyclic aromatic hydrocarbons (PAHs) in a Mars chamber, emulating the ultraviolet spectrum of unfiltered sunlight under temperature and pressure conditions of the Martian surface. Fluorescence spectroscopy is used as a sensitive indicator of remaining PAH concentration for laboratory quantification of molecular degradation rates once exposed on the Martian surface. Fluorescence‐based instrumentation has also been proposed as an effective surveying method for prebiotic organics on the Martian surface. We find the representative PAHs, anthracene, pyrene, and perylene, to have persistence half‐lives once exposed on the Martian surface of between 25 and 60 h of noontime summer UV irradiation, as measured by fluorescence at their peak excitation wavelength. This equates to between 4 and 9.6 sols when the diurnal cycle of UV light intensity on the Martian surface is taken into account, giving a substantial window of opportunity for detection of organic fluorescence before photodegradation. This study thus supports the use of fluorescence‐based instrumentation for surveying recently exposed material (such as from cores or drill tailings) for native Martian organic molecules in rover missions.     

Martian cratering 12. Utilizing primary crater clusters to study crater populations and meteoroid properties

Images from Mars Global Surveyor and later images from Mars Reconnaissance Orbiter reveal that roughly half of the meteoroids striking Mars (at meter to few decameter crater diameters) fragment in the Martian atmosphere, producing small clusters of primary impact craters. Statistics of these “primary clusters” yield valuable information about important Martian phenomena and properties of interplanetary bodies, including meteoroid behavior in the Martian atmosphere, bulk strengths of bodies striking Mars, and the fraction of Martian “field secondary” craters, a datum that would improve crater count chronometry. Many Martian impactors fragment at altitudes significantly higher than 18 km above the mean surface of Mars, and we find that most bodies striking Mars and Earth have low bulk strengths, consistent with crumbly or highly fractured objects. Applying statistics of primary clusters at various elevations and independent diameter bins, we describe a technique to estimate the percentage of semirandomly scattered “field secondary” craters. Our provisional estimate of this percentage, in the diameter range ~250 m down to ~22 m, is ~40% to ~80% of the total impacts, with the higher percentages at smaller diameters. Our data argue against earlier suggestions of overwhelming dominance by either primaries or secondaries in this diameter range.     

Magnetized Mars: Transformation of Earth-like magnetosphere to Venus-like induced magnetosphere

Using a global numerical model, we have studied how the present Martian magnetosphere may have looked in the past when the planet had a global intrinsic magnetic field. A Mars version (HYB-Mars) of the self-consistent quasi-neutral hybrid model was used which treats the ions as particles and the electrons as a massless charge-neutralizing fluid. We compare four cases where an intrinsic dipole magnetic field was 0 nT (the present situation), 10, 30, and 60 nT at the surface of Mars along the magnetic equator. We find that the 10 nT dipolar magnetic field already results in a magnetosphere which in many respects is more Earth-like than, a non-magnetized, “induced” magnetosphere. However, the 10 nT dipole magnetosphere is still relatively strongly connected to the interplanetary magnetic field, while the 30 nT dipole case, and especially the 60 nT dipole case, results in a magnetosphere whose morphology is determined predominantly by the Martian intrinsic magnetic field. A change of the magnetosphere due to a decreasing dipole magnetic field strength from 60 to 0 nT could have happened during the history of Mars when a globally magnetized Mars turned into the present, globally non-magnetized, planet.     

Ion loss on Mars caused by the Kelvin-Helmholtz instability

Mars Global Surveyor detected cold electrons above the Martian ionopause, which can be interpreted as detached ionospheric plasma clouds. Similar observations by the Pioneer Venus Orbiter electron temperature probe showed also extreme spatial irregularities of electrons in the form of plasma clouds on Venus, which were explained by the occurrence of the Kelvin-Helmholtz instability. Therefore, we suggest that the Kelvin-Helmholtz instability may also detach ionospheric plasma clouds on Mars. We investigate the instability growth rate at the Martian ionopause resulting from the flow of the solar wind for the case where the interplanetary magnetic field is oriented normal to the flow direction. Since the velocity shear near the subsolar point is very small, this area is stable with respect to the Kelvin-Helmholtz instability. We found that the highest flow velocities are reached at the equatorial flanks near the terminator plane, while the maximum plasma density in the terminator plane appears at the polar areas. By comparing the instability growth rate with the magnetic barrier formation time, we found that the instability can evolve into a non-linear stage at the whole terminator plane but preferably at the equatorial flanks. Escape rates of O⁺ ions due to detached plasma clouds in the order of about 2×10²³-3×10²⁴ s^-1 are found. Thus, atmospheric loss caused by the Kelvin-Helmholtz instability should be comparable with other non-thermal loss processes. Further, we discuss our results in view of the expected observations of heavy ion loss rates by ASPERA-3 on board of Mars Express.     

Methods for the analysis of data from the Planetary Fourier Spectrometer on the Mars Express Mission

This work presents an algorithm for the scientific analysis of individual calibrated measurements from the Planetary Fourier spectrometer (PFS).The instrument, included in the scientific payload of the ESA Mars Express mission to Mars, acquires spectra in the range between 250 and 8200 cm⁻¹, with a sampling step of ∼1 cm⁻¹ and an effective resolution of ∼2 cm⁻¹. The observed radiance depends on several parameters of the atmosphere and surface of Mars as described by the radiative transfer equation. Adopting the very general formalism of Bayesian analysis, we determined which quantities are actually retrievable from individual measurements. Namely, they are: the surface temperature, the column density of dust and water ice aerosols in the atmosphere, the air temperature as a function of altitude (in the indicative range 5-45 km above the surface), the surface pressure, and the column density of water vapor and carbon monoxide. These evaluations are carried out taking into account the noise equivalent radiance (NER) of the instrument and the natural variabilities of the investigated parameters in the Martian environment, as estimated from the expectations of the European Martian Climate Dataset v3.1 (EMCD). Other parameters included in the radiative transfer equation shall be assumed as known, because they are not retrievable from individual measurements due to the instrumental NER or an underconstrained inverse problem: the surface emissivity in the thermal infrared, the optical properties of suspended dust and the analytical shape of dust concentration vs. altitude.During the development of the algorithm devoted to these studies, different approaches were evaluated on the basis of formal, computational and scientific considerations, with the aim to develop the general design of an integrated software package.The resulting code was extensively tested on a wide set of simulated PFS spectra. These spectra were computed from the atmospheric and surface conditions extracted from the EMCD, assumed to be representative of the Martian environment for different values of latitude, local time and season. Their comparison with the retrievals from simulated observations allowed us to evaluate the systematic and random errors affecting the procedures with respect to the different quantities involved. The code evaluates the surface temperature with an error in the order of 1 K, while the vertical air temperature profile is computed with an uncertainty less than 2 K from in the region between 5 and 20 km above the surface, increasing up to 7 K at 50 km. The column opacity of dust, measured in terms of integrated optical thickness at 1100 cm⁻¹, is computed with an error of around 0.13. The surface pressure determination is carried out with a typical uncertainty of 0.2-0.3 millibar. Several auxiliary tests allowed us to study the correlations between the different retrieval errors and the possible causes of incorrect PFS data interpretation. The choice of a suitable model for the dust optical properties is demonstrated to be particularly critical.This paper also presents the first discussion about application of the procedure to actual PFS Martian data. Despite the calibration issues still affecting the determination of absolute radiance in the near-infrared, the algorithm is able to achieve a satisfactory modeling of observations in a wide range of situations.     

A new extraction technique for in situ analyses of amino and carboxylic acids on Mars by gas chromatography mass spectrometry

In order to target key organic compounds in the Martian regolith using gas chromatography mass spectrometry (GC-MS), we have developed a new extraction procedure coupled with chemical derivatization. This new technique was tested on a Mars analog soil sample collected from the Atacama Desert in Chile. We found that amino and carboxylic acids can be extracted from the Atacama soil in a 1:1 mixture of isopropanol and water after ultrasonic treatment for 30 min. The extracted organic compounds were then derivatized in a single-step reaction using N-methyl-N-(tert-butyldimethylsilyl)-trifluoroacetamide (MTBSTFA) as the silylating agent in order to transform these compounds into volatile species that can then be detected by GC-MS. We are currently developing a miniaturized reaction cell suited for spaceflight, where both organic extraction and chemical derivatization processes can take place in a single step.     

On the properties of O and O2 ions in a hybrid model and in Mars Express IMA/ASPERA-3 data: A case study

We have performed a numerical simulation to analyze the energy spectra of escaping planetary O⁺ and O₂⁺ ions at Mars. The simulated time-energy spectrograms were generated along orbit no. 555 (June 27, 2004) of Mars Express when its Ion Mass Analyzer (IMA)/ASPERA-3 ion instrument detected escaping planetary ions. The simulated time-energy spectrograms are in general agreement with the hypothesis that planetary O⁺ and O₂⁺ ions far from Mars are accelerated by the convective electric field. The HYB-Mars hybrid model simulation also shows that O⁺ ions originating from the ionized hot oxygen corona result in a high-energy (E>1 keV) O⁺ ion population that exists very close to Mars. In addition, the simulation also results in a low-energy (E<0.1 keV) planetary ion population near the pericenter. In the analyzed orbit, IMA did not observe a clear high-energy planetary ion or a clear low-energy planetary ion population near Mars. One possible source for this discrepancy may be the Martian magnetic crustal anomalies because MEX passed over a strong crustal field region near the pericenter, but the hybrid model does not include the magnetic crustal anomalies.     

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.