Hydrothermal alteration of impact melt sheets with implications for Mars

A model of the interaction of water with an impact melt sheet is constructed to explain the presence of hydrothermal alteration, fluid flow channels, and the redistribution of volatile elements in terrestrial melt sheets. A calculation of the amount of water vaporized beneath a melt sheet with a large fraction of melt results in a maximum total steam/melt sheet ratio of 23% by weight. The model also applies to Martian impact melt sheets, which have a total volume greater than a global layer 60 m thick. Hydrothermal circulation of steam in Martian melt sheets may have produced iron-rich alteration clays, ferric hydroxides, and near-surface accumulations of salts. The ability of vapor-dominated hydrothermal systems of concentrate sulfate relative to chloride is consistent with the high sulfate to chloride ratio found in the Martian soil by the Viking landers. A major fraction of the Martian soil may consist of the erosion products of hydrothermally altered impact melt sheets.     

Ries Bunte Breccia revisited: Indications for the presence of water in Itzing and Otting drill cores and implications for the emplacement process

We reassessed two drill cores of the Bunte Breccia deposits of the Ries crater, Germany. The objectives of our study were the documentation of evidence for water in the Bunte Breccia, the evaluation of how that water influenced the emplacement processes, and from which preimpact water reservoir it was derived. The Bunte Breccia in both cores can be structured into a basal layer composed mainly of local substrate material, overlain by texturally and compositionally diverse, crater‐derived breccia units. The basal layer is composed of the youngest sediments (Tertiary clays and Upper Jurassic limestone) and has a razor‐sharp boundary to the upper breccia units, which are composed of older rocks of Upper Jurassic to Upper Triassic age. Sparse material exchange occurred between the basal layer and the rest of the Bunte Breccia. Fluids predominantly came from the Tertiary and the Upper Triassic sandstone formation. In the basal layer, Tertiary clays were subjected to intense, ductile deformation, indicating saturation with water. This suggests that water was mixed into the matrix, creating a fluidized basal layer with a strong shear localization. In the upper units, Upper Triassic sandstones are intensely deformed by granular flow. The texture requires that the rocks were disaggregated into granular sand. Vaporization of pore water probably aided fragmentation of these rocks. In the Otting core, hot suevite (T > 600 °C) covered the Bunte Breccia shortly after its emplacement. Vertically oriented gas escape pipes in suevite partly emanate directly at the contact to the Bunte Breccia. They indicate that the Bunte Breccia contained a substantial amount of water in the upper part that was vaporized and escaped through these vents.     

Hydration state of zeolites, clays, and hydrated salts under present-day martian surface conditions: Can hydrous minerals account for Mars Odyssey observations of near-equatorial water-equivalent hydrogen?

Thermodynamic data for several clays, zeolites, and MgSO₄ salts were combined with calculated yearly mean temperatures and water-vapor pressures on the martian surface to predict mineral hydration states from low to middle latitudes. These predictions were used to evaluate whether the necessary amount and distribution of hydrous minerals were compatible with the Mars Odyssey observations of water-equivalent hydrogen (WEH). Our results indicate that zeolites like chabazite or clay minerals like Ca-montmorillonite would have to be unrealistically abundant in the martian soil (as much as 55 wt%) while Mg-sulfate hydrates at concentrations between 2 and 11 wt% could account for the WEH. However, the geographic distribution of WEH is incompatible with a uniformly distributed mineralogy in equilibrium with the annual mean P-T environment. A heterogeneous distribution of a mixture of different hydrous minerals, reflecting a heterogeneous Mars surface geology, may better explain a significant portion of the observed near-equatorial WEH.     

The 1.7- to 4.2-μm spectrum of asteroid 1 Ceres: Evidence for structural water in clay minerals

A high-resolution Fourier spectrum (1.7–3.5 μm) and medium-resolution spectrophotometry (2.7–4.2 μm) were obtained for Asteroid 1 Ceres. The presence of the 3-μm absorption feature due to water of hydration was confirmed. The 3-μm feature is compared with the 3-μm bands due to water of hydration in clays and salts. It is concluded that the spectrum of Ceres shows a strong absorption at 2.7–2.8 μm due to structural OH groups in clay minerals. The dominant minerals on the surface of Ceres are therefore hydrated clay minerals structurally similar to terrestrial montmorillonites. There is also a narrow absorption feature at 3.1 μm which is attributable to a very small amount of water ice on Ceres. This is the first evidence for ice on the surface of an asteroid.     

Preterrestrial aqueous alteration of the Lafayette (SNC) meteorite

Abstract— The Lafayette meteorite, a nakhlite of the SNC (Martian?) group, contains hydrous alteration materials as intergranular films and as veinlets and patches replacing olivine, pyroxenes, and high-Si glass. The alteration materials (“iddingsite”) consist of ferroan smectite clays, magnetite (or maghemite), and ferrihydrite, as shown by SEM and TEM. Three varieties of veinlets are present and formed in the order: coarse phyllosilicate; fine-grained (phyllosilicate-oxide), and porous oxide. Veinlets of fine-grained material cross-cut coarse phyllosilicate veinlets. The alteration materials are preterrestrial, as they are older than Lafayette's fusion crust, which is glassy and not affected by any alterations. Approaching the crust, the veinlets are progressively modified to the point of melting, and progressively depleted in adsorbed volatile constituents (S, Cl, and P). Bulk compositions of the alteration veinlets (SEM and TEM EDX) are consistent with the observed mineralogy, and suggest: that the smectite contains significant adsorbed S and Cl; that the ferrihydrite contains significant adsorbed S, but not Cl; that rare grains of sulfate (Ca?) and chloride (Na or K?) are present; and that the compositions of the alteration materials are approximated by Lafayette's olivine + high-Si glass + water. We estimate that Lafayette's alteration materials formed at less than 100 °C. The oxidation potential of the water was near or slightly below that of the magnetite-hematite buffer. The presence of sulfate and chloride in discrete phases and as adsorbates on ferrihydrite and smectite suggests that the altering solutions were saline. However, relatively little mass was transferred into or out of Lafayette because the bulk composition of the alteration materials is nearly isochemical with a mixture of magmatic silicate phases and water. Chemical transport within Lafayette was also limited, as alteration materials preserve some chemical signature of their host minerals. Presence of alteration materials along only some grain boundaries and some cracks suggests that Lafayette was not soaked in fluid. These last two inferences suggest that the alteration of Lafayette took place during episodic infiltrations of small volumes of saline water.     

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.     

Mars low-latitude neutron distribution: Possible remnant near-surface water ice and a mechanism for its recent emplacement

The Mars Odyssey Gamma-Ray Spectrometer/Neutron Spectrometer/High Energy Neutron Detector has provided measurements of near-surface hydrogen, generally interpreted as resulting from water, in the equatorial and mid-latitudes. Water abundances as great as 10% by mass are inferred. Although such high abundances could be present as adsorbed water in clays or water of hydration of magnesium salts, other measurements suggest that this is not likely. The spatial pattern of where the water is located is not consistent with a dependence on composition, topography, present-day atmospheric water abundance, latitude, or thermophysical properties. The zonal distribution of water shows two maxima and two minima, which is very reminiscent of a distribution that is related to an atmospheric phenomenon. We suggest that the high water abundances could be due to transient ground ice that is present in the top meter of the surface. Ice would be stable at tens-of-centimeters depth at these latitudes if the atmospheric water abundance were more than about several times the present value, much as ice is stable poleward of about ±60° latitude for current water abundances. Higher atmospheric water abundances could have resulted relatively recently, even with the present orbital elements, if the south-polar cap had lost its annual covering of CO₂ ice; this would have exposed an underlying water-ice cap that could supply water to the atmosphere during southern summer. If this hypothesis is correct, then (i) the low-latitude water ice is unstable today and is in the process of sublimating and diffusing back into the atmosphere, and (ii) the current configuration of perennial CO₂ ice being present on the south cap but not on the north cap might not be representative of the present epoch over the last, say, ten thousand years.     

Weathering of Mars: Antarctic analog studies

Terrestrial analog studies of potential Martian weathering processes are reported. Four major weathering environments are identified: (i) hydrothermal alteration of impact melt sheets and impact breccias, (ii) solid-gas and related reactions, (iii) subpermafrost intrusion of lavas involving liquid water, and (iv) subaerial extrusion of lavas in the absence of liquid water. Weathering in environments (i)?(iii) has been discussed by other authors; this report discusses weathering in environment (iv), an analog of which is Antarctica. We conclude that weathering is geologically slow in the absence of liquid water, and that zeolites predominate over clays as secondary minerals. On volumetric grounds it appears that hydrothermal alteration of impact melt sheets should be the most important time-averaged weathering mechanism, provided that H₂O was present as liquid or permafrost. Such hydrothermal alteration should operate predominately on ancient crustal material. Gas-solid reactions and photochemical weathering should also operate primarily on ancient crustal material on a time-averaged basis. Weathering products of younger subpermafrost or subaerially erupted basalts should be subordinate to hydrothermal alteration and gas-solid reactions. It appears that the present Martian regolith as analyzed by the Viking landers contains a major contribution from ancient crust as typified today by the southern cratered highlands, with a lesser contribution from the younger, hemispherically restricted basaltic lavas.     

Ceres's global and localized mineralogical composition determined by Dawn's Visible and Infrared Spectrometer (VIR)

The Visible and Infrared Spectrometer (VIR) instrument on the Dawn mission observed Ceres’s surface at different spatial resolutions, revealing a nearly uniform global distribution of surface mineralogy. Clearly, Ceres experienced extensive water‐related processes and chemical differentiation. The surface is mainly composed of a dark component (carbon, magnetite?), Mg‐phyllosilicates, ammoniated clays, carbonates, and salts. The observed species suggest endogenous, global‐scale aqueous alteration. While mostly uniform at regional scale, Ceres’s surface shows small localized areas with different species and/or variations in abundances. Few local exposures of water ice are seen, especially at higher latitudes. Sodium carbonates have been identified in several areas on the surface, notably in Occator bright faculae. Organic matter has also been discovered in several places, most conspicuously in a large area close to the Ernutet crater. The observed mineralogies, with the presence of ammoniated species and sodium salts, have a strong resemblance to materials found on other bodies of the outer solar system, such as Enceladus. This poses some questions about the original material from which Ceres accreted, suggesting a colder environment for such material with respect to Ceres’s present position.     

The surface composition of Ceres: Discovery of carbonates and iron-rich clays

We present observational evidence that carbonates and iron-rich clays are present on the surface of Ceres. These components are also present in CI chondrites and provide a means of explaining the unusual spectrum of this object as well as providing potential insight into its evolution.     

Prebiotic carbon in clays from Orgueil and Ivuna (CI), and Tagish Lake (C2 ungrouped) meteorites

Abstract— Transmission electron microscopic (TEM) and electron energy‐loss spectroscopic (EELS) study of the Ivuna and Orgueil (CI), and Tagish Lake (C2 ungrouped) carbonaceous chondrite meteorites shows two types of C‐clay assemblages. The first is coarser‐grained (to 1 μm) clay flakes that show an intense O K edge from the silicate together with a prominent C K edge, but without discrete C particles. Nitrogen is common in some clay flakes. Individual Orgueil and Tagish Lake meteorite clay flakes contain up to 6 and 8 at% C, respectively. The C K‐edge spectra from the clays show fine structure revealing aromatic, aliphatic, carboxylic, and carbonate C. The EELS data shows that this C is intercalated with the clay flakes. The second C‐clay association occurs as poorly crystalline to amorphous material occurring as nanometer aggregates of C, clay, and Fe‐O‐rich material. Some aggregates are dominated by carbonaceous particles that are structurally and chemically similar to the acid insoluble organic matter. The C K‐edge shape from this C resembles that of amorphous C, but lacking the distinct peaks corresponding to aliphatic, carboxylic, and carbonate C groups. Nanodiamonds are locally abundant in some carbonaceous particles. The abundance of C in the clays suggest that molecular speciation in the carbonaceous chondrites is partly determined by the effects of aqueous processing on the meteorite parent bodies, and that clays played an important role. This intricate C‐clay association lends credence to the proposal that minerals were important in the prebiotic chemical evolution of the early solar system.     

Río Tinto sedimentary mineral assemblages: A terrestrial perspective that suggests some formation pathways of phyllosilicates on Mars

The presence of extensive phyllosilicate deposits from the early Noachian of Mars are often interpreted as having formed from neutral to subalkaline solutions. In this paper we examine the Río Tinto fluvial basin, an early Mars analog, that hosts clay production and sedimentation along the entire course of the river. At Río Tinto, phyllosilicate minerals including clays and micas are sourced by volcanosedimentary bedrock of rhyolitic and andesitic composition affected by Carboniferous hydrothermal alteration. Pleistocene to modern acidic weathering of those materials chemically altered the volcanic and sedimentary materials to K/Na-clay-(montmorillonite/smectites)-kaolinite assemblages in paleosoils and fractures while physical weathering degrades phyllosilicates more resistant to acidic attack. During the wet season, phyllosilicates are eroded, transported and deposited from both acidic headwaters and neutral tributaries. During the dry season, sulfates and nanophase oxyhydroxides co-precipitate. Late summer storms that cause fast flooding events mix illite, quartz, feldspars, iron oxides and other minerals in fluvial deposits where these minerals are stabilized and aggrade until the following wet season. As a result, chemical precipitates, primary phyllosilicates and secondary clays form mineral admixtures that explain the compositional diversity of the fluvial deposits. These deposits reveal the persistence of smectites, whose occurrence is explained given that the reaction kinetics under acidic conditions of degradation is lowered by seasonal discharges of the river. The longevity of phyllosilicate minerals within fluvial deposits depends on climatic and geochemical conditions and processes which are in turn are correlated to temperature, persistence of water, hydrological cycling, hydrogeochemistry and composition of the source materials in the basement. These parameters are universal and have to be characterized in order to understand the distribution of mineral composition on any planetary surface, including Mars.     

Water ice polymorphs and their significance on planetary surfaces

Impacts into an icy surface could produce significant amounts of high pressure forms of water ice. Due to the relatively low ambient surface temperatures on satellites in the outer solar system and the modest temperature rises accompanying the impact pressures required for water ice metamorphism, high-pressure polymorphs will be created by and may remain after large cratering events. If so, those high-pressure ices should be ubiquitous. Low-pressure cubic ice may be abundant as well. Impacts into an icy regolith may both produce high-pressure polymorphs from ice I and destroy high-pressure polymorphs already present. The result will be an (unknown) equilibrium concentration of high pressure polymorphs in the regolith. Polymorphs may be detectable and mappable by reflection spectroscopy at vacuum ultraviolet and mid-infrared wavelengths.     

Carbonates and sulfates in the Chassigny meteorite: Further evidence for aqueous chemistry on the SNC parent planet

Abstract— Scanning electron microscopy and energy-dispersive X-ray spectrometry of untreated interior chips from three different specimens of the Chassigny meteorite confirm the presence of discrete grains of Ca-carbonate, Mg-carbonate, and Ca-sulfate. Morphologies of these salt grains suggest that the Ca-carbonate is calcite (CaCO₃) and that the Ca-sulfate is gypsum (CaSO₄·2H₂O) or bassanite (CaSO₄·1/2H₂O). The morphologic identification of the Mg-carbonate is equivocal, but rhombohedral and acicular crystal habits suggest magnesite and hydromagnesite, respectively. The salts in Chassigny occur as discontinuous veins in primary igneous minerals and are similar to those previously documented in the nakhlites, Nakhla and Lafayette, and in shergottite EETA79001. Unlike those in nakhlites, however, the Chassigny salts occur alone, without associated ferric oxides or aluminosilicate clays. Traces of Cl and P in Chassigny salts are consistent with precipitation of the salts from short-lived, saline, aqueous solutions that postdated igneous crystallization. In contrast with the clear case for nakhlites, stratigraphic evidence for a preterrestrial origin of the salts in Chassigny is ambiguous; however, a preterrestrial origin of the Chassigny salts best explains all available evidence. The water-precipitated salts provide clear physical evidence for the hypothesis, proposed by other workers, that the igneous amphiboles in Chassigny might have experienced isotope-exchange reactions with near-surface water, thereby compromising the original stable-isotope signature of any magmatic water in melt inclusions.     

Ceres internal structure from geophysical constraints

Thermal evolution modeling has yielded a variety of interior structures for Ceres, ranging from a modestly differentiated interior to more advanced evolution with a dry silicate core, a hydrated silicate mantle, and a volatile‐rich crust. Here we compute the mass and hydrostatic flattening from more than one hundred billion three‐layer density models for Ceres and describe the characteristics of the population of density structures that are consistent with the Dawn observations. We show that the mass and hydrostatic flattening constraints from Ceres indicate the presence of a high‐density core with greater than a 1σ probability, but provide little constraint on the density, allowing for core compositions that range from hydrous and/or anhydrous silicates to a mixture of metal and silicates. The crustal densities are consistent with surface observations of salts, water ice, carbonates, and ammoniated clays, which indicate hydrothermal alteration, partial fractionation, and the possible settling of heavy sulfide and metallic particles, which provide a potential process for increasing mass with depth.     

Evolution of Io's volatile inventory

Using Voyager results, we have made crude estimates of the rate at which Io loses volatiles by a variety of processes to the surrounding magnetosphere for both the current SO₂-dominated atmosphere as well as hypothetical paleoatmospheres in which other gases, such as N₂, may have been the dominant constituent. Loss rates are strongly influenced by the surface pressure on the night side, the relationship between the exobase and the Jovian magnetospheric boundary, the exospheric temperature, and the peak altitudes reached by volcanic plumes. Several mechanisms make significant contributions to the prodigious rate at which Io is currently losing volatiles. These include: interaction of the magnetospheric plasma with volcanic plume particles and the background atmosphere; sputtering of ices on the surface, if the nightside atmospheric pressure is low enough; and Jeans' escape of O, a dissociation product of SO₂ gas. For paleoatmospheres, only the first two of these mechanisms would have been effective. However, they are capable of eliminating large amounts of N₂ and other volatiles from Io over the satellite's lifetime. Io could have also lost large amounts of water over its lifetime due to the extensive recycling of water between its upper and lower crust, with the partial dissociation of water vapor in silicate magma chambers initiating this loss process. Significant amounts of water may also have been lost as a result of the interaction of the magnetospheric plasma with water ice particles in volcanic plumes. Once an SO₂-dominated atmosphere becomes established, much water may have also been lost through the sputtering of surface water ice.     

The stability of water in Io

A variety of processes have been examined to determine their impact on water loss from Io and the formation of an anhydrous surface. Thermal escape, photolysis, and gas-phase charged particle interactions are shown to be unimportant in this regard. Recent laboratory experiments have shown that charged-particle sputtering is likely to be an effective mechanism for the removal of water ice from Io's surface. Vaporization of ice by meteoroid impacts may also be significant. The overall sputtering rate appears to be sufficiently high that the formation of a substantial regolith due to meteoroid bombardment will be prevented. However, meteoroid bombardment is probably capable of maintaining a thin (? 500 μm overturned surface layer from which all free water has been removed by sputtering. Alternatively, a thick anhydrous surface layer may have formed on Io as the result of primordial heating. The survival of such a layer to the present implies the absence of subsequent water evolution onto the surface of the satellite.     

Sutter's Mill dicarboxylic acids as possible tracers of parent‐body alteration processes

Dicarboxylic acids were searched for in three Sutter's Mill (SM) fragments (SM2 collected prerain, SM12, and SM41) and found to occur almost exclusively as linear species of 3‐ to 14‐carbon long. Between these, concentrations were low, with measured quantities typically less than 10 nmole g^?1 of meteorite and a maximum of 6.8 nmole g^?1 of meteorite for suberic acid in SM12. The SM acids' molecular distribution is consistent with a nonbiological origin and differs from those of CMs, such as Murchison or Murray, and of some stones of the C2‐ungrouped Tagish Lake meteorite, where they are abundant and varied. Powder X‐ray diffraction of SM12 and SM41 show them to be dominated by clays/amorphous material, with lesser amounts of Fe‐sulfides, magnetite, and calcite. Thermal gravimetric (TG) analysis shows mass losses up to 1000 °C of 11.4% (SM12) and 9.4% (SM41). These losses are low compared with other clay‐rich carbonaceous chondrites, such as Murchison (14.5%) and Orgueil (21.1%). The TG data are indicative of partially dehydrated clays, in accordance with published work on SM2, for which mineralogical studies suggest asteroidal heating to around 500 °C. In view of these compositional traits and mineralogical features, it is suggested that the dicarboxylic acids observed in the SM fragments we analyzed likely represent a combination of molecular species original to the meteorite as well as secondary products formed during parent‐body alteration processes, such as asteroidal heating.     

Martian lake basins and lacustrine plains

Outflow channels and valley systems are evidence of water flow on the surface of Mars. Whenever there is a consequent flow of water on an irregular surface, temporary impoundment in surface depressions will form lakes. A classification of martian lake basins based on the location of the basin in respect to water sources is proposed. The classes are Type 1: Valley-head basins, Type 2: Intravalley basins, Type 3: Valley-terminal basins, and Type 4: Isolated basins.Martian lakes are ephemeral features. Many craters and irregular depressions impounded water only until the basins filled and overflowed. Water escaping by spillover rapidly cut crevasses in the downstream side of basins and drained the ponds. Clastic lacustrine sediments collected in the lakes as flowing water lost velocity and turbulence. Evaporitic deposits may be significant in those basins that were not rapidly drained. Sediments deposited in lake basins form smooth, featureless plains. Lacustrine plains are potentially candidate sites for Mars landings and for the search for evidence of ancient life.     

Late Glacial beech forest: an 18,000–5000-BP pollen record from Auckland, New Zealand

Australia, New Zealand and South America are the main sources of terrestrial climate change records for midlatitudes in the Southern Hemisphere. The advantage of studying the New Zealand record is that its vegetation has been subject to human influence for only the last thousand years. Vegetation records for Auckland are important because earlier work indicates that during the Last Glacial Maximum, the boundary between scrubland and forest lay in the Auckland region. Auckland is situated in a volcanic field and the coring site was in the crater of a small extinct volcano (Crater Hill, formed about 29 ka BP). The 4-m long core contained sediment dating from c. 5 to c. 18 ka BP. We present pollen and diatom records from this core.The pollen records from basal clays indicate southern beech forest (mainly Nothofagus menziesii) was present in the region around Crater Hill from 18 to 14.5 ka BP. At this time, there were areas of scrub in the crater surrounding a hardwater lake. The southern forest limit could well have been close to the site. Records from overlying peat indicate beech forest was replaced by Podocarp broadleaf forest as the Last Glacial ended. Metrosideros spp. (coastal forest trees) peak in the early Holocene. This coincides with an impoverished diatom flora which indicates drier conditions in the basin. When the lake reformed in the Holocene on peat its water was more acidic.