Martian cratering revisited: Implications for early geologic evolution

Improved crater statistics from varied Martian terrains are compared to lunar crater populations. The distribution functions for the average Martian cratered terrain and the average lunar highlands over the diameter range 8–2000 km are quite similar. The Martian population is less dense by approximately 0.70 from 8 to 256 km diameter and diverges to proportionally lower densities at greater diameters. Crater densities on Martian “pure” terra give a lower limit to the Mars/Moon integrated crater flux of 0.75 since the last stabilization of the respective planetary crusts. The crater population >8 km diameter postdating the Martian northern plains is statistically indistinguishable from that population postdating the lunar maria. Monte Carlo simulations were performed to constrain plausible mechanisms of crater obliteration. The models demonstrate that if the crater density difference between the lunar and Martian terra has been due to resurfacing processes, random intercrater plains formation cannot be the sole process. If plains preferentially form in and obliterate larger craters, then the observed Martian distribution retains its “shape” as the crater density decreases. This result is consistent with the morphology of Martian intercrater plains.     

Constraints on the water,chlorine, and fluorine content of the Martian mantle

Previous estimates of the volatile contents of Martian basalts, and hence their source regions, ranged from nearly volatile‐free through estimates similar to those found in terrestrial subduction zones. Here, we use the bulk chemistry of Martian meteorites, along with Martian apatite and amphibole chemistry, to constrain the volatile contents of the Martian interior. Our estimates show that the volatile content of the source region for the Martian meteorites is similar to the terrestrial Mid‐Ocean‐Ridge Mantle source. Chlorine is enriched compared with the depleted terrestrial mantle but is similar to the terrestrial enriched source region; fluorine is similar to the terrestrial primitive mantle; and water is consistent with the terrestrial mantle. Our results show that Martian magmas were not volatile saturated; had water/chlorine and water/fluorine ratios ~0.4–18; and are most similar, in terms of volatiles, to terrestrial MORBs. Presumably, there are variations in volatile content in the Martian interior as suggested by apatite compositions, but more bulk chemical data, especially for fluorine and water, are required to investigate these variations. Finally, the Noachian Martian interior, as exemplified by surface basalts and NWA 7034, may have had higher volatile contents.     

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.     

火星磁层中O^＋离子分布的理论研究

对火星磁层中背阳面区来自电离层的Ｏ＋离子沿磁力线的密度和通量密度分布进行了理论研究．设火星的磁场由内禀磁场和感应磁场相叠加而成,结合不同的内禀磁矩条件进行了计算．结果表明：（１）随着火心距离的增大,火星磁层中Ｏ＋离子的密度和通量密度沿磁力线都呈现出下降趋势;（２）随着Ｚ坐标的增大,火星磁层中Ｏ＋离子的密度和通量密度先呈现出下降趋势,后又逐渐上升;（３）火星的内禀磁场越强,Ｏ＋离子的密度和通量密度沿磁力线下降得越快;（４）在火星磁尾一定距离处,Ｏ＋离子的密度和通量密度随磁矩的增大而减小．这样,可通过探测火星磁层中离子的密度和通量密度分布来确定火星内禀磁场的强弱     

Differential transmission of sunlight on Mars: Biological implications

A euphotic zone seems to exist at about 1 cm subsurface in the Martian epilith. At this depth visible light is still intense enough to be utilized by conceivable photosynthetic organisms; but the germicidal ultraviolet intensities at the Martian surface have been reduced to values manageable by terrestrial life. Such euphotic zone organisms would experience moderately high Martian temperatures at equatorial latitudes and can be dispersed readily during global dust stroms. During such storms the Martian euphotic zone may reach the surface. The aerosol content of the Martian atmosphere can be monitored by multiband single line scans of the sun at large zenith angles by the Viking lander camera; and the postulated euphotic zone organisms can be searched for with the Viking lander sample arm and biology experiments.     

Comparison between infrared Martian disk spectra and optical properties of terrestrial analogs

Medium spectral resolution (20 cm^?1) infrared measurements of the Martian disk made between 2900 and 5600 cm^?1 from the NASA Lear Airborne Observatory have been successfully compared with predictions derived from a model of the Martian soil and atmosphere. Modeling of the Martian atmosphere permitted the extraction of Martian soil reflectance in the CO₂ bands centered at 3657 cm^?1. Three previously considered acceptable Martian soil analogs, limonite, montmorillonite, and basalt, were analyzed to determine the optical complex indices of refraction in the same range as the airborne observations, for mathematical modeling. A characteristic surface particle size ～1 to 3 μm diameter is indicated. It is concluded that the Martian soil surface near-infrared optical properties are consistent with a soil composition similar to montmorillonite or limonite, mixed with a basalt.     

Issues and options for a Martian calendar

In the past 125 years, more than 70 authors have published ideas for keeping time on Mars, describing how to divide the Martian day and Martian year into smaller units. The Martian prime meridian was established in the mid-19th century, and the design of the Martian clock has been standardised at least since the Viking missions of the 1970s. Scientists can tell time on Mars; however, despite the constant stream of data that is downlinked from Mars these days, there is still no standardised system for expressing the date on Mars. Establishing a standard epoch—at a specific time of year on Mars, and a specific Martian year—should be the next priority in Martian timekeeping as a minimal system required for the physical sciences. More elaborate ideas, including the number and length of weeks and months, and names thereto, can be deferred for the present, but may become important considerations in coming years.     

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.     

The chlorine isotopic composition of Martian meteorites 1: Chlorine isotope composition of Martian mantle and crustal reservoirs and their interactions

The Martian meteorites record a wide diversity of environments, processes, and ages. Much work has been done to decipher potential mantle sources for Martian magmas and their interactions with crustal and surface environments. Chlorine isotopes provide a unique opportunity to assess interactions between Martian mantle‐derived magmas and the crust. We have measured the Cl‐isotopic composition of 17 samples that span the range of known ages, Martian environments, and mantle reservoirs. The ³⁷Cl of the Martian mantle, as represented by the olivine‐phyric shergottites, NWA 2737 (chassignite), and Shergotty (basaltic shergottite), has a low value of approximately ?3.8‰. This value is lower than that of all other planetary bodies measured thus far. The Martian crust, as represented by regolith breccia NWA 7034, is variably enriched in the heavy isotope of Cl. This enrichment is reflective of preferential loss of ³⁵Cl to space. Most basaltic shergottites (less Shergotty), nakhlites, Chassigny, and Allan Hills 84001 lie on a continuum between the Martian mantle and crust. This intermediate range is explained by mechanical mixing through impact, fluid interaction, and assimilation‐fractional crystallization.     

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.     

Orbital observations of meteors in the Martian atmosphere using the SPOSH camera

We investigate the expected performance of a wide-angle camera in Martian orbit, which, unlike previous cameras that have flown to Mars, is capable of recording meteor activity in that planet's atmosphere. We show that, based on our current understanding of meteor physics and the interplanetary meteoroid population, several meteors will be detected by this instrument during a single nightside pass on a low Martian orbit. The instrument will also record the signatures of meteor showers expected to occur every Martian year (1.88 Earth years). The results of this investigation will test models of the flux of “large” (mm-cm) meteoroids at the orbit of Mars and their interaction with the Martian atmosphere.     

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.     

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.     

Heterogeneous distribution of H2O in the Martian interior: Implications for the abundance of H2O in depleted and enriched mantle sources

We conducted a petrologic study of apatite within 12 Martian meteorites, including 11 shergottites and one basaltic regolith breccia. These data were combined with previously published data to gain a better understanding of the abundance and distribution of volatiles in the Martian interior. Apatites in individual Martian meteorites span a wide range of compositions, indicating they did not form by equilibrium crystallization. In fact, the intrasample variation in apatite is best described by either fractional crystallization or crustal contamination with a Cl‐rich crustal component. We determined that most Martian meteorites investigated here have been affected by crustal contamination and hence cannot be used to estimate volatile abundances of the Martian mantle. Using the subset of samples that did not exhibit crustal contamination, we determined that the enriched shergottite source has 36–73 ppm H₂O and the depleted source has 14–23 ppm H₂O. This result is consistent with other observed geochemical differences between enriched and depleted shergottites and supports the idea that there are at least two geochemically distinct reservoirs in the Martian mantle. We also estimated the H₂O, Cl, and F content of the Martian crust using known crust‐mantle distributions for incompatible lithophile elements. We determined that the bulk Martian crust has ~1410 ppm H₂O, 450 ppm Cl, and 106 ppm F, and Cl and H₂O are preferentially distributed toward the Martian surface. The estimate of crustal H₂O results in a global equivalent surface layer (GEL) of ~229 m, which can account for at least some of the surface features on Mars attributed to flowing water and may be sufficient to support the past presence of a shallow sea on Mars' surface.     

A technique to deduce atmospheric temperature and constituent profiles from a planet's limb radiance profile

The concept is described of deducing the temperature and constituent profile of a planetary atmosphere from orbiter measurements of the planet's ir limb radiance profile. Expressions are derived for the weighting functions associated with the limb radiance profile for a Goody random band model. Analysis of the weighting functions for the Martian atmosphere indicates that a limb radiance profile in the 15 μm CO₂ band can be used to determine the Martian atmospheric temperature profile from 20 to 60 km. Simulation of the Martian limb radiance profile in the rotational water vapor band indicates that Martian water vapor mixing ratios can be inferred from limb radiance observations in a water vapor band.     

Comparison of knobs on mars to isolated hills in eolian,fluvial and glacial environments

Positive isolated features or knobs have been observed on Mars since Mariner 9 first photographed the planet in 1972. More recently, the Viking Orbiters photographed the surface at increased resolution. With the use of Viking photomosaics, a systematic search for knobs was completed. The knobs were characterized by length, width, geographic location, proximity to streaks and geologic surroundings. Similar isolated features on Earth eroded by fluvial, glacial, and eolian processes were studied and measured. Comparison of length-to-width ratios of Martian knobs to isolated hills on Earth indicate that the Martian knobs are most similar to the isolated hills formed in a hyper-arid environment. The terrestrial features were probably formed initially when solid rock was fractured, then wind erosion, starting at the fractures, continued to sweep away sediments leaving isolated hills. Such hills in fluvial and glacial environments have length-to-width ratios significantly higher than those of the Martian knobs. Other diagnostic features associated with such environments are absent in the case of the Martian knobs. Moreover, streaks, splotches, dunes and pitted and fluted rocks, all indicative of a eolian regime, are associated with the Martian knobs.     

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.     

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.     

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%.     

Helium in the Martian atmosphere: Thermal loss considerations

Helium concentrations in the Martian atmosphere are estimated assuming that the helium production on Mars, comparable to its production on Earth, via the radioactive decay of uranium and thorium, is in steady state equilibrium with its thermal escape. Although non-thermal losses would tend to reduce the estimated concentrations, these concentrations are not necessarily an upper limit since higher production rates and/or a possibly lower effective exospheric temperature over the solar activity cycle could increase them to even higher values. The computed helium concentration at the Martian exobase (200 km) is 8 × 10⁶ atoms cm^?3. Through the lower exosphere, the computed helium concentrations are 30–200 times greater than the Mariner-measured atomic hydrogen concentrations. It follows that helium may be the predominant constituent in the Martian lower exosphere and may well control the orbital lifetime of Mars-orbiting spacecraft. The estimated helium mixing ratio is greater at the Martian turbopause than at the terrestrial turbopause, and the helium column density in the lower Martian atmosphere may be comparable to that on Earth.