Experimental hydrothermal alteration of a martian analog basalt: Implications for martian meteorites

Abstract— A number of martian meteorite samples contain secondary alteration minerals such as Ca‐Mg‐Fe carbonates, Fe oxides, and clay minerals. These mineral assemblages hint at hydrothermal processes occurring in the martian crust, but the alteration conditions are poorly constrained. This study presents the results of experiments that examined the alteration of a high‐Fe basalt by CO₂‐saturated aqueous fluids at 23 and 75 °C and by mixed H₂O‐CO₂ vapors at 200 and 400 °C and water‐rock ratios of 1:1 and 1:10. Results indicate that observable alteration of the basalt takes place after runs of only seven days. This alteration includes mobilization of silica into phases such as opal‐CT and quartz, as well as the formation of carbonates, oxides, and at some conditions, zeolites and hydrous silicates. The degree of alteration increases with run temperature and, in high‐temperature vapor experiments, with increasing water content of the vapor. The degree of alteration and the mineralogy observed in the martian meteorites suggests that none of these samples were exposed to aqueous fluids for long periods of time. Nakhla and Lafayette probably interacted with water for relatively brief periods of time; if so, silica may have been leached from the parent rocks by the altering fluids. Allan Hills 84001 shows possible evidence for very limited interaction with an aqueous fluid, but the overall slight degree of alteration described for this meteorite strongly suggests that it never interacted extensively or at high temperature with any water‐bearing fluid. Elephant Moraine A79001 may not have been altered by aqueous fluids at all. The results of this study best support models wherein the meteorite parent rocks were wetted intermittently or for brief periods of time rather than models that invoke long‐term reaction with large volumes of water. Our experiments studied alteration of a high‐Fe basalt by dilute, CO₂‐saturated, aqueous solutions at 23 and 75 °C and by mixed H₂O‐CO₂ vapors at 200 and 400 °C. The results suggest that alteration of the parent rock takes place even after very short reaction times of seven days. All experiments produced carbonate minerals, including calcite, and in some cases, magnesite, siderite, and ankerite. A free silica phase, either opal, quartz, or hydrated silica, formed in most experiments. More altered experiments also contained minerals such as zeolites and hydrous phyllosilicates. Clay minerals were not observed to form in any experiments. In aqueous fluids, higher temperature corresponded with a higher degree of alteration, whereas changing fluid composition had no observable effect. In high‐temperature vapors, the degree of alteration was controlled by temperature and the proportion of H₂O to CO₂, with water‐rock ratio also playing a role in transport of silica. Application of these results to martian meteorites that contain secondary alteration minerals suggests that none of the martian rocks underwent extensive interaction with aqueous fluids. Nakhla and Lafayette contain clay minerals, which suggests that they interacted with water to some extent, possibly at elevated temperatures. Although ALH84001 shows possible evidence of very limited interaction with aqueous fluids, EETA79001 does not. These results support models for the alteration of these meteorites that do not invoke long‐term interaction with water or reaction with large volumes of water. Except for some models for alteration of ALH84001, this conclusion agrees with most of the literature on alteration of martian meteorites.     

Experimental hydrothermal alteration of basaltic glass with relevance to Mars

Phyllosilicates, carbonates, zeolites, and sulfates on Mars give clues about the planet's past environmental conditions, but little is known about the specific conditions in which these minerals formed within the crust and at the surface. The aim of the present study was to gain increased understanding on the formation of secondary phases by hydrothermal alteration of basaltic glass. The reaction processes were studied under varying conditions (temperature, pCO₂, water:rock ratio, and fluid composition) with relevance to aqueous hydrothermal alteration in fully and partly saturated Martian basalt deposits. Analyses made on reaction products using X‐ray diffraction (XRD) and scanning electron microscope (SEM) were compared with near infrared spectroscopy (NIR) to establish relative detectability and spectral signatures. This study demonstrates that comparable alteration minerals (phyllosilicates, carbonates, zeolites) form from vapor condensing on mineral surfaces in unsaturated sediments and not only in fully water‐saturated sediments. In certain environments where water vapor might be present, it can alter the basaltic bedrock to a suite of authigenic phases similar to those observed on the Martian surface. For the detection of the secondary phases, XRD and SEM‐EDS were found to be superior to NIR for detecting and characterizing zeolites. The discrepancy in detectability of zeolites between NIR and XRD/SEM‐EDS might indicate that zeolites on Mars are more abundant than previously thought.     

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.     

Possible melting produced chondrule destruction in NWA 6604 CK4 chondrite

In analyzing a thin section of the NWA 6604 CK4 meteorite, only altered chondrules and various components that are probably left behind the destruction of former chondrules can be observed. We suggest that melting, grain size decrease, resorption of the original chondrules, and crystallization of opaque minerals were the main processes that destroyed the chondrules. Four different events could be identified as having occurred during this alteration. First, opaques crystallized along former fractures producing chains of separated grains. Later, opaques and Ca‐rich minerals crystallized together in veins and large melt pockets; this was the strongest recrystallization phase involving the largest volume of melt. This occurred along different fractures than the first phase above. During the third phase, only Ca‐rich plagioclase crystallized along thin veins, and in a fourth phase, fractures formed again, partly along those formed during the second phases but without substantial mineral infill. Two simple possible case models should be considered for this meteorite: alteration by purely impact‐driven processes or mainly by melt‐driven processes. Although for CK4 chondrites, the shock‐produced alteration driven by impact is the more accepted and widespread approach, melting is also compatible with the observed textural characteristics of chondrule destruction. During melting, recrystallization took place producing iron‐rich minerals earlier and Ca‐Si‐rich ones later. The penetration of melts into veins contributed in the chondrule destruction. The stress directions also changed during these alterations, and minerals that formed later filled differently oriented fractures than the earlier ones. From our observations, we favor a view where heat‐driven melting and recrystallization produced the destruction and uniform mineralogy in the sample.     

The Kaidun meteorite: Mineralogy of an unusual CM1 lithology

Abstract Kaidun is a breccia of disparate enstatite and carbonaceous chondrite clasts that continues to provide real surprises. Many Kaidun clasts have been intensely altered by aqueous fluids, as evidenced by the widespread occurrence of ferromagnesian phyllosilicates and by the presence of carbonate- and phyllo-silicate-filled veins. In this report, we describe an unusual CM lithology containing many mineralogical features not previously reported from any meteorite, including pyrrhotite, with exclusive needlelike morphologies and thick mantles of phyllosilicate, and complex aggregates of phyllosilicate, melanite garnet, crosscut by pentlandite veins. The latter features appear to be due in large part to extensive hydrothermal alteration at temperatures on the order of 450 °C, which is significantly higher than that attained during secondary processing from other known CM material.     

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.     

Epitaxial fluorapatite vein in Northwest Africa 998 host apatite: Clues on the geochemistry of late hydrothermal fluids on Mars

Secondary minerals in martian nakhlites provide a powerful tool for investigating the nature, composition, and duration of aqueous activity in the martian crust. Northwest Africa (NWA) 998 crystallized early from the nakhlite magmatic source and has evidence of minimal signatures of the late hydrothermal alteration event that altered the nakhlites. Using FIB-TEM techniques to study a cumulus apatite grain in NWA 998, we report the first evidence of a submicron-scale vein consisting of fluorapatite and an SiO₂-rich phase. Fluorapatite grew epitaxially on the walls of an opened cleavage plane of host F-bearing chlorapatite and the SiO₂-rich phase filled the center of the vein. The presence of nanoporosity and nanometer-scale amorphous material and the sharp interface between the vein and the host apatite indicate the vein represents a coupled dissolution–reprecipitation process that generated apatite of a different composition that was more stable with the fluid. Using experimental data and diffusion coefficients of Cl in apatite from the literature, we conclude that the vein was caused by a low temperature (~300°C), slightly acidic, F-, Si-rich, aqueous fluid that acted as a closed system. Based on the characteristics of the vein (formation by rapid injection of fluid) and the fluid (composition, temperature, pH), and the lack of terrestrial weathering products in our SEM and TEM images, we infer that the vein is pre-terrestrial in origin. Our observations support the hypothesis that the heat source triggering a hydrothermal system was a low-shock velocity impact and rule out a magmatic origin. Finally, the vein could have formed from a late-stage fluid different from that reported in other nakhlites, but formation during the same magmatic event by, for example, a less evolved fluid might also be plausible.     

The distinct morphological and petrological features of shock melt veins in the Suizhou L6 chondrite

Abstract– The morphology and petrology of distinct melt veins in the Suizhou L6 chondrite have been investigated using scanning electron microscopy, electron microprobe analyses, and Raman spectroscopy, synchrotron energy‐dispersive diffraction, and transmission electron microscopy. It is found that the melt veins in the Suizhou meteorite morphologically are the simplest, straightest, and thinnest among all shock veins known from meteorites. At first glance, these veins look like fine fractures, but petrologically they are solid melt veins of chondritic composition and consist of fully crystalline materials of two distinct lithological assemblages, with no glassy material remaining. The Suizhou melt veins contain the most abundant high‐pressure mineral species when compared with all other veins known in chondrites. Thus, these veins in Suizhou are classified as shock veins. All rock‐forming and almost all accessory minerals in the Suizhou shock veins have been transformed to their high‐pressure polymorphs, and no fragments of the precursor minerals remain in the veins. Among the 11 high‐pressure mineral phases identified in the Suizhou veins, three are new high‐pressure minerals, namely, tuite after whitlockite, xieite, and the CF phase after chromite. On the basis of transformation of plagioclase into maskelynite, it is estimated that the Suizhou meteorite experienced shock pressures and shock temperatures up to 22 GPa and 1000 °C, respectively. Shearing and friction along shock veins raised the temperature up to 1900–2000 °C and the pressure up to 24 GPa within the veins. Hence, phase transition and crystallization of high‐pressure minerals took place only in the Suizhou shock veins. Fast cooling of the extremely thin shock veins is regarded as the main reason that up to 11 shock‐induced high‐pressure mineral phases could be preserved in these veins.     

Opaque assemblages in CR2 Graves Nunataks (GRA) 06100 as indicators of shock‐driven hydrothermal alteration in the CR chondrite parent body

We have studied the petrologic characteristics of sulfide‐metal lodes, polymineralic Fe‐Ni nodules, and opaque assemblages in the CR2 chondrite Graves Nunataks (GRA) 06100, one of the most altered CR chondrites. Unlike low petrologic type CR chondrites, alteration of metal appears to have played a central role in the formation of secondary minerals in GRA 06100. Differences in the mineralogy and chemical compositions of materials in GRA 06100 suggest that it experienced higher temperatures than other CR2 chondrites. Mineralogic features indicative of high temperature include: (1) exsolution of Ni‐poor and Ni‐rich metal from nebular kamacite; (2) formation of sulfides, oxides, and phosphates; (3) changes in the Co/Ni ratios; and (4) carbidization of Fe‐Ni metal. The conspicuous absence of pentlandite may indicate that peak temperatures exceeded 600 °C. Opaques appear to have been affected by the action of aqueous fluids that resulted in the formation of abundant oxides, Fe‐rich carbonates, including endmember ankerite, and the sulfide‐silicate‐phosphate scorzalite. We suggest that these materials formed via impact‐driven metamorphism. Mineralogic features indicative of impact metamorphism include (1) the presence of sulfide‐metal lodes; (2) the abundance of polymineralic opaque assemblages with mosaic‐like textures; and (3) the presence of suessite. Initial shock metamorphism probably resulted in replacement of nebular Fe‐Ni metal in chondrules and in matrix by Ni‐rich, Co‐rich Fe metal, Al‐Ti‐Cr‐rich alloys, and Fe sulfides, while subsequent hydrothermal alteration produced accessory oxides, phosphates, and Fe carbonates. An extensive network of sulfide‐metal veins permitted effective exchange of siderophile elements from pre‐existing metal nodules with adjacent chondrules and matrix, resulting in unusually high Fe contents in these objects.     

Fluids during diagenesis and sulfate vein formation in sediments at Gale crater,Mars

We model the fluids involved in the alteration processes recorded in the Sheepbed Member mudstones of Yellowknife Bay (YKB), Gale crater, Mars, as revealed by the Mars Science Laboratory Curiosity rover investigations. We compare the Gale crater waters with fluids modeled for shergottites, nakhlites, and the ancient meteorite ALH 84001, as well as rocks analyzed by the Mars Exploration rovers, and with terrestrial ground and surface waters. The aqueous solution present during sediment alteration associated with phyllosilicate formation at Gale was high in Na, K, and Si; had low Mg, Fe, and Al concentrations—relative to terrestrial groundwaters such as the Deccan Traps and other modeled Mars fluids; and had near neutral to alkaline pH. Ca and S species were present in the 10^?3 to 10^?2 concentration range. A fluid local to Gale crater strata produced the alteration products observed by Curiosity and subsequent evaporation of this groundwater‐type fluid formed impure sulfate‐ and silica‐rich deposits—veins or horizons. In a second, separate stage of alteration, partial dissolution of this sulfate‐rich layer in Yellowknife Bay, or beyond, led to the pure sulfate veins observed in YKB. This scenario is analogous to similar processes identified at a terrestrial site in Triassic sediments with gypsum veins of the Mercia Mudstone Group in Watchet Bay, UK.     

Magmatic cristobalite and quartz in the NWA 856 Martian meteorite

Abstract— Silica‐rich late‐stage crystallization pockets in the Martian meteorite Northwest Africa (NWA) 856 were investigated by transmission electron microscopy (TEM). The pockets occur as wedges between maskelynite laths or between maskelynite and pyroxene. They consist of elongated grains of cristobalite and quartz embedded in a silica‐rich glass. Interstitial to the amorphous phase and silica minerals, a number of small accessory minerals have been identified, typical for late‐stage crystallization products. They are ilmenite, tranquillityite, fayalite, troilite, baddeleyite, apatite, and chloroapatite. Cristobalite and quartz are shocked, as revealed by the occurrence of numerous amorphous lamellae. This assemblage suggests metastable dendritic crystallization under hydrous conditions. Cristobalite crystallization was probably facilitated by the presence of impurities such as Na or H₂O. Our observations show that silica minerals can be formed under magmatic conditions on Mars.     

Alteration assemblages in the nakhlites: Variation with depth on Mars

Secondary mineral assemblages in the nakhlite meteorites, Lafayette, Governador Valadares (GV), Nakhla, Yamato (Y)‐000593/Y‐000749 have been studied using scanning electron microscopy, transmission electron microscopy, and electron probe micro analysis. The different nakhlites have distinctive secondary assemblages in their olivine grains and mesostases, showing compositional fractionation correlated with their relative depths below the Martian surface. Fracture‐filled veins in Lafayette at the bottom of the pile consist of a siderite‐phyllosilicate‐Fe oxide‐hydrated silicate gel assemblage. Corresponding veins in Nakhla and GV further up the pile are predominantly a siderite‐gel assemblage, with additional evaporites including gypsum. Y‐000593/Y‐000749 veins are dominated by gel. The gel’s Mg/(Mg + Fe) ratio decreases from Lafayette (0.37) to GV (0.32), Nakhla (0.24), and Y‐000593 (0.15). We suggest that hydrothermal fluid flowed up this depth profile, initiated by melting of buried H₂O–CO₂ ice. Our results show a complex mix of Fe‐rich phyllosilicate within the veins and mesostasis of Lafayette with d‐spacings of 0.7–1.1 nm suggesting a mixture of smectite and serpentine. The phyllosilicate formed at close to neutral pH, ≤150 °C. We also suggest that water rock ratios (W/R) of 1–10 occurred in Lafayette with smaller values for the other nakhlites. This is reflected in the volume of alteration minerals: 10% of olivine in Lafayette to 3% in Nakhla. Textural evidence of rapid cooling, together with the W/R and likely fluid velocities, suggest that the secondary assemblages formed quickly, e.g., within months. A model is proposed in which the secondary assemblages formed in an impact‐induced hydrothermal system terminated by precipitation of the gel and evaporation of soluble salts.     

Comprehensive imaging and Raman spectroscopy of carbonate globules from Martian meteorite ALH 84001 and a terrestrial analogue from Svalbard

Abstract— We report a comprehensive imaging study including confocal microRaman spectroscopy, scanning electron microscopy (SEM), and 3‐D extended focal imaging light microscopy of carbonate globules throughout a depth profile of the Martian meteorite Allan Hills (ALH) 84001 and similar objects in mantle peridotite xenoliths from the Bockfjorden volcanic complex (BVC), Svalbard. Carbonate and iron oxide zoning in ALH 84001 is similar to that seen in BVC globules. Hematite appears to be present in all ALH 84001 carbonate‐bearing assemblages except within a magnesite outer rim found in some globules. Macromolecular carbon (MMC) was found in intimate association with magnetite in both ALH 84001 and BVC carbonates. The MMC synthesis mechanism appears similar to established reactions within the Fe‐C‐O system. By inference to a terrestrial analogue of mantle origin (BVC), these results appear to represent the first measurements of the products of an abiotic MMC synthesis mechanism in Martian samples. Furthermore, the ubiquitous but heterogeneous distribution of hematite throughout carbonate globules in ALH 84001 may be partly responsible for some of the wide range in measured oxygen isotopes reported in previous studies. Using BVC carbonates as a suitable analogue, we postulate that a low temperature hydrothermal model of ALH 84001 globule formation is most likely, although alteration (decarbonation) of a subset of globules possibly occurred during a later impact event.     

Hydrothermal alteration in the core of the Yaxcopoil‐1 borehole,Chicxulub impact structure,Mexico

Abstract Petrographic, electron microprobe, and Raman spectrometric analyses of Yaxcopoil‐1 core samples from the Chicxulub crater indicate that the impact generated a hydrothermal system. Relative textural and vein crosscutting relations and systematic distribution of alteration products reveal a progression of the hydrothermal event in space and time and provide constraints on the nature of the fluids. The earliest calcite, halite, and gaylussite suggest that the impactite sequence was initially permeated by a low temperature saline brine. Subsequent development of a higher temperature hydrothermal regime is indicated by thermal metamorphic diopside‐hedenbergite (Aeg₃Fs_18‐33En_32‐11Wo_47‐53) after primary augite and widespread Na‐K for Ca metasomatic alkali exchange in plagioclase. Hydrothermal sphene, apatite, magnetite + (bornite), as well as early calcite (combined 3 to 8 vol%) were introduced with metasomatic feldspar. A lower temperature regime characterized by smectite after probable primary glass, secondary chlorite, and other pre‐existing mafic minerals, as well as very abundant calcite veins and open‐space fillings, extensively overprinted the early hydrothermal stage. The composition of early and late hydrothermal minerals show that the solution was chlorine‐rich (Cl/F >10) and that its Fe/Mg ratio and oxidation state increased substantially (4 to 5 logfO₂ units) as temperature decreased through time. The most altered zone in the impactite sequence occurs 30 m above the impact melt. The lack of mineralogical zoning about the impact melt and convective modeling constraints suggest that this unit was too thin at Yaxcopoil‐1 to provide the necessary heat to drive fluids and implies that the hydrothermal system resulted from the combined effects of a pre‐existing saline brine and heat that traveled to the Yaxcopoil‐1 site from adjacent areas where the melt sheet was thicker. Limonite after iron oxides is more common toward the top of the sequence and suggests that the impactite section was subjected to weathering before deposition of the Tertiary marine cover. In addition, scarce latest anatase stringers, chalcopyrite, and barite in vugs, francolite after apatite, and recrystallized halite are the likely products of limited post‐hydrothermal ambient‐temperature diagenesis, or ocean and/or meteoric water circulation.     

The petrography,mineralogy and origins of calcium sulphate within the Cold Bokkeveld CM carbonaceous chondrite

Abstract— A detailed scanning and transmission electron microscopy study of Cold Bokkeveld has shown that calcium sulphate is widespread, occluding ～30 μm wide matrix-cutting fractures in addition to μm-sized veins and irregular dissolution pores within calcitized chondrules, matrix calcite grains and Ca- and Al-rich inclusions (CAI). The majority of calcium sulphate crystals have fibrous habits, especially those which have grown within straight-sided fractures and veins. Mineralogically, the calcium sulphate is composed of a fine-scale mixture of hemihydrate and anhydrite which have probably formed by the dehydration of primary gypsum during sample preparation. In all contexts, calcium sulphate precipitation was the last identifiable diagenetic event in the pre-terrestrial history of Cold Bokkeveld and followed pervasive aqueous alteration of the meteorite matrix to phyllosilicates. The fibrous fracture- and vein-filling calcium sulphates are morphologically similar to a terrestrial form of gypsum termed “satinspar” and so may have formed in a similar manner by precipitation from supersaturated aqueous solutions during fracture and vein dilation. The aqueous solutions were most probably generated by melting of water ice due to internal heating and/or post-accretional impact heating of the parent body. Although impact-produced fractures and veins may have provided conduits for fluid advection, the dissolution of calcite, alteration of metal sulphides and precipitation of gypsum probably took place when aqueous solutions were more-or-less static. Despite their similarity to late-stage mineralized fractures in CI meteorites, the calcium sulphate-filled fractures in Cold Bokkeveld probably do not have any significance regarding a shared CM-CI parent body.     

Low‐temperature phase decomposition in iron‐nickel metal of the Portales Valley meteorite

Abstract— The Portales Valley meteorite provides an opportunity to investigate and compare the microstructure in Fe‐Ni metal of the metallic particles in the chondritic portion and in the metal veins. The low‐temperature phase decomposition of Fe‐Ni metal was investigated using scanning electron microscopy, transmission electron microscopy, and atomic force microscopy. The microstructure is formed as the Portales Valley meteorite cooled from high temperatures and includes the outer taenite rim, the cloudy zone, clear taenite, and martensite. Martensite in turn decomposes into a fine admixture of fcc rods in a bcc matrix. The width of the island phase of the cloudy zone in the metal particles of the chondritic portion and the metal veins can be used to estimate a low‐temperature cooling rate. The microstructural evidence indicates that the chondritic portions and the metal veins in the Portales Valley meteorite cooled together as a mixture with a cooling rate of roughly 6.5 K/Ma.     

Hydrothermal alteration at the Lonar Lake impact structure,India: Implications for impact cratering on Mars

Abstract— The 50,000 year old, 1.8 km diameter Lonar crater is one of only two known terrestrial craters to be emplaced in basaltic target rock (the 65 million year old Deccan Traps). The composition of the Lonar basalts is similar to martian basaltic meteorites, which establishes Lonar as an excellent analogue for similarly sized craters on the surface of Mars. Samples from cores drilled into the Lonar crater floor show that there are basaltic impact breccias that have been altered by post‐impact hydrothermal processes to produce an assemblage of secondary alteration minerals. Microprobe data and X‐ray diffraction analyses show that the alteration mineral assemblage consists primarily of saponite, with minor celadonite, and carbonate. Thermodynamic modeling and terrestrial volcanic analogues were used to demonstrate that these clay minerals formed at temperatures between 130°C and 200°C. By comparing the Lonar alteration assemblage with alteration at other terrestrial craters, we conclude that the Lonar crater represents a lower size limit for impact‐induced hydrothermal activity. Based on these results, we suggest that similarly sized craters on Mars have the potential to form hydrothermal systems, as long as liquid water was present on or near the martian surface. Furthermore, the Fe‐rich alteration minerals produced by post‐impact hydrothermal processes could contribute to the minor iron enrichment associated with the formation of the martian soil.     

Aqueous alteration of the Nakhla meteorite

Abstract— Interior samples of three different Nakhla specimens contain an iron-rich silicate “rust” (which includes a tentatively identified smectite), Ca-carbonate (probably calcite), Ca-sulfate (possibly gypsum or bassanite), Mg-sulfate (possibly epsomite or kieserite), and NaCl (halite); the total abundance of these phases is estimated as <0.01 weight percent of the bulk meteorite. Rust veins are truncated and decrepitated by fusion crust and are preserved as faulted segments in partially healed olivine crystals, indicating that the rust is pre-terrestrial in origin. Because Ca-carbonate and Ca-sulfate are intergrown with the rust, they are also indicated to be of pre-terrestrial origin. Similar textural evidence regarding origins of the NaCl and Mg-sulfate is lacking. Impure and poorly crystallized sulfates and halides on the fusion crust of the meteorite suggest leaching of interior (pre-terrestrial) salts from the interior after Nakhla arrived on Earth but coincidental addition of these same salts by terrestrial contamination cannot be excluded. At least the clay-like silicate “rust,” Ca-carbonate, and Ca-sulfate were formed by precipitation from water-based solutions on the Nakhla parent planet although temperature and pressure conditions of aqueous precipitation are unconstrained by currently available data. It is possible that aqueous alteration on the parent body was responsible for the previously observed disturbance of the Rb-Sr geochronometer in Nakhla at or near 1.3 Ga.     

Fluid inclusion evidence for impact‐related hydrothermal fluid and hydrocarbon migration in Creataceous sediments of the ICDP‐Chicxulub drill core Yax‐1

Fluid inclusions studies in quartz and calcite in samples from the ICDP‐Chicxulub drill core Yaxcopoil‐1 (Yax‐1) have revealed compelling evidence for impact‐induced hydrothermal alteration. Fluid circulation through the melt breccia and the underlying sedimentary rocks was not homogeneous in time and space. The formation of euhedral quartz crystals in vugs hosted by Cretaceous limestones is related to the migration of hot (>200 °C), highly saline, metal‐rich, hydrocarbon‐bearing brines. Hydrocarbons present in some inclusions in quartz are assumed to derive from cracking of pre‐impact organic matter. The center of the crater is assumed to be the source of the hot quartz‐forming brines. Fluid inclusions in abundant newly‐formed calcite indicate lower cyrstallization temperatures (75–100 °C). Calcite crystallization is likely related to a later stage of hydrothermal alteration. Calcite precipitated from saline fluids, most probably from formation water. Carbon and oxygen isotope compositions and REE distributions in calcites and carbonate host rocks suggest that the calcite‐forming fluids have achieved close equilibrium conditions with the Cretaceous limestones. The precipitation of calcite may be related to the convection of local pore fluids, possibly triggered by impact‐induced conductive heating of the sediments.     

Secondary alteration of the impactite and mineralization in the basal Tertiary sequence,Yaxcopoil‐1, Chicxulub impact crater,Mexico

Abstract The 65 Ma Chicxulub impact crater formed in the shallow coastal marine shelf of the Yucatán Platform in Mexico. Impacts into water‐rich environments provide heat and geological structures that generate and focus sub‐seafloor convective hydrothermal systems. Core from the Yaxcopoil‐1 (Yax‐1) hole, drilled by the Chicxulub Scientific Drilling Project (CSDP), allowed testing for the presence of an impact‐induced hydrothermal system by: a) characterizing the secondary alteration of the 100 m‐thick impactite sequence; and b) testing for a chemical input into the lower Tertiary sediments that would reflect aquagene hydrothermal plume deposition. Interaction of the Yax‐1 impactites with seawater is evident through redeposition of the suevites (unit 1), secondary alteration mineral assemblages, and the subaqueous depositional environment for the lower Tertiary carbonates immediately overlying the impactites. The least‐altered silicate melt composition intersected in Yax‐1 is that of a calc‐alkaline basaltic andesite with 53.4–56 wt% SiO_{2(volatile‐free)}. The primary mineralogy consists of fine microlites of diopside, plagioclase (mainly Ab 47), ternary feldspar (Ab 37 to 77), and trace apatite, titanite, and zircon. The overprinting alteration mineral assemblage is characterized by Mg‐saponite, K‐montmorillonite, celadonite, K‐feldspar, albite, Fe‐oxides, and late Ca and Mg carbonates. Mg and K metasomatism resulted from seawater interaction with the suevitic rocks producing smectite‐K‐feldspar assemblages in the absence of any mixed layer clay minerals, illite, or chlorite. Rare pyrite, sphalerite, galena, and chalcopyrite occur near the base of the impactites. These secondary alteration minerals formed by low temperature (0–150°C) oxidation and fixation of alkalis due to the interaction of glass‐rich suevite with down‐welling seawater in the outer annular trough intersected at Yax‐1. The alteration represents a cold, Mg‐K‐rich seawater recharge zone, possibly recharging higher temperature hydrothermal activity proposed in the central impact basin. Hydrothermal metal input into the Tertiary ocean is shown by elevated Ni, Ag, Au, Bi, and Te concentrations in marcasite and Cd and Ga in sphalerite in the basal 25 m of the Tertiary carbonates in Yax‐1. The lower Tertiary trace element signature reflects hydrothermal metal remobilization from a mafic source rock and is indicative of hydrothermal venting of evolved seawater into the Tertiary ocean from an impact‐generated hydrothermal convective system.