火星古湖泊研究的现状、问题与展望

火星表面的古湖泊地貌能够反映火星古气候和古环境的特征及变化,对于研究火星是否曾经存在宜居环境具有重要意义.随着中国火星探测计划的提出和实施,详细了解火星古湖泊的研究进展尤为重要.总结了火星古湖泊的研究现状,重点阐述了当前对火星古湖泊的沉积地貌、矿物成分、形成年龄、分布特征等方面的研究进展.在综合分析前人研究成果的基础上,提出火星古湖泊研究中存在的主要问题,认为未来应着重在古湖泊的详细调查与地质填图、古湖泊的后期改造作用、其他类型古湖泊的识别分析以及火星与地球古湖泊的对比等方面开展研究.      

火星陨石和火星表面泥岩中蚀变过程对比研究

火星次生含水蚀变矿物是火星地质历史时期水环境和气候演变历史的真实记录,一直以来都是火星探测、火星陨石研究的重点,是认识火星环境特征和气候演化的重要研究对象。文中对比研究了表土角砾岩NWA7034、火成堆晶岩MIL03346等两块最富蚀变矿物火星陨石,以及Gale撞击坑出露的Sheepbed泥岩3种岩石类型的蚀变程度及其蚀变矿物类型和组合,分析了层状硅酸盐、铁氧化物/氢氧化物、钙硫酸盐等蚀变矿物的成因及环境指示意义。发现这3类岩石的蚀变作用各不相同。火星陨石NWA7034的蚀变作用以氧化和加热作用为主,无蒸发盐类矿物。火星陨石MIL03346的蚀变程度最低,为后期水溶液进入缝隙而引发的,蚀变作用以橄榄石的伊利石化、裂隙和缝隙中填充次生矿物细脉为主。而火星Sheepbed泥岩经历了后期的等化学风化过程(isochemical weathering),次生过程包括成岩蚀变和成岩后蚀变两个阶段。其中,成岩过程中的蚀变以橄榄石蚀变为铁氧化物和蒙皂石矿物为主,成岩后以形成蒸发盐类矿物硫酸钙为主。以上3种岩石蚀变矿物组成差异反映了火星上不同地质背景中、不同气候条件下蚀变过程的复杂性。文中对火星含水矿物及部分典型矿物的形成条件和过程进行系统总结,这对于理解未来火星探测任务、识别含水矿物的形成、揭示火星水环境和地质历史具有重要指导意义。     

Petrology and shock metamorphism of the olivine-phyric shergottite Yamato 980459: Evidence for a two-stage cooling and a single-stage ejection history

The basaltic Martian meteorite Yamato 980459 consists of large olivine phenocrysts and often prismatic pyroxenes set into a fine-grained groundmass of smaller more Fe-rich olivine, chromite, and an interstitial residual material displaying quenching textures of dendritic olivine, chain-like augite and sulfide droplets in a glassy matrix. Yamato 980459 is, thus, the only Martian meteorite without plagioclase/maskelynite. Olivine is compositionally zoned from a Mg-rich core to a Fe-rich rim with the outer few micrometers being especially rich in iron. With Fo₈₄ the cores are the most magnesian olivines found in Martian meteorites so far. Pyroxenes are also mostly composite crystals of large orthopyroxene cores and thin Ca-rich overgrowths. Separate pigeonite and augites are rare. On basis of the mineral compositions, the cooling rates determined from crystal morphologies, and crystal grain size distributions it is deduced that the parent magma of Yamato 980459 initially cooled under near equilibrium conditions e.g., in a magma chamber allowing chromite and the Mg-rich silicates to form as cumulus phases. Fractional crystallization at higher cooling rates and a low degree of undercooling let to the formation of the Ca-, Al-, and Fe-rich overgrowths on olivine and orthopyroxene while the magma was ascending towards the Martian surface. Finally and before plagioclase and also phosphates could precipitate, the magma was very quickly erupted quenching the remaining melt to glass, dendritic silicates and sulfide droplets. The shape preferred orientation of olivine and pyroxene suggests a quick, thin outflow of lava. According to the shock effects found in the minerals of Yamato 980459, the meteorite experienced an equilibration shock pressure of about 20-25 GPa. Its near surface position allowed the ejection from the planet’s surface already by a single impact event and at relatively low shock pressures.     

Identifying when microbes biosilicify: The interconnected requirements of acidic pH, colloidal SiO2 and exposed microbial surface

This study demonstrates discernible biosilicification of natural microbial mats through batch laboratory experiments. Identification of the geochemical requirements for this process to occur includes thermodynamically favorable, but sluggish silica reaction kinetics associated with acidic conditions, and the necessity for colloidal silica rather than dissolved silicic acid species. This study provides the first results to bridge the apparent literature discrepancy between widespread, in-situ observations of microbial silicification, and the inability to demonstrate a detectable microbial impact in this process under well-constrained laboratory conditions. We compared the silica scavenging abilities of three natural microbial mats collected from Yellowstone National Park (YNP) hotsprings, relative to those of both abiotic particle (TiO₂) and solution controls at constant, near-saturated aqueous silica concentrations, while experimental pH and temperature conditions were varied, using both dissolved and colloidal SiO₂ forms. We specifically evaluated three microbial mats sampled from YNP sites all exhibiting saturation with respect to amorphous SiO₂, but possessing variable pH and temperature conditions that should reflect differential kinetics (and therefore biological opportunity) relative to silica polymerization: (1) most biologically favorable, acidic-mesophile (AM: pH 3, T = 35 °C); (2) biologically possible, but less opportune, alkaline, mesophile (ALK-M: pH 8, T = 35 °C) and (3) unlikely to be biologically favorable, alkaline-thermophile (ALK-T: pH 8, T = 80 °C). Comparison of field and laboratory results substantiates the requirements for thermodynamically favorable, but kinetically slower SiO₂ polymerization conditions. Results show that acidic moderate temperature conditions were required for an observable biosilicification impact. Moreover, they also identified for the first time, the necessity specifically for colloidal silica forms which are surface bound under acidic pH conditions, to distinguish discernible biosilicification compared to mineral particle controls. Results also highlight the important influence of mat surface characteristics in this process, specifically the extent of live, non-mineralized, exposed biological mat surface. Greater colloidal SiO₂ scavenging abilities are associated with non-mineralized microbial mat surfaces than with mineral particle surfaces or microbial mat surfaces encrusted with authigenic silica. These results are the first to demonstrate that biosilicification can be a microbially mediated, discernible geobiological process, shedding new light on the longstanding argument in the literature, and opening the door for more sensitive evaluation of this phenomenon in natural systems.     

A Review of Magnesium Isotope System in Rivers

In recent years, a series of important progresses have been made in the aspect of magnesium isotopes behavior in weathering processes. These progresses are not only favorable to understand the change of the magnesium isotopic compositions in rivers, but also establish the foundation to further reveal the magnesium isotope geochemical cycle. The magnesium in rivers is both magnesium sink for weathering and magnesium source for the ocean. The Mg isotopic compositions in rivers are dominated by the magnesium sources and Mg isotope fractionations processes. The sources of magnesium in rivers originate mainly from draining rocks, as well as less contribution from the eolian deposition, groundwater, plant debris, and precipitation. The Mg isotope fractionations in rivers are mainly related to precipitation and dissolution of carbonate minerals, silicate mineral hydrolysis, adsorption on mineral or colloidal matter surface, and plant uptake. Generally, the contribution of carbonate minerals dissolution or precipitation is equal to add or reduce magnesium from carbonate endmember, which has a remarkably negative δ²⁶Mg value. Based on the fact that most clay minerals are rich in ²⁶Mg during nature silicate mineral hydrolysis, then it is possible to infer that residual weathering products enrich in ²⁶Mg. However, there is no significant Mg isotope fractionation causing by the adsorption on mineral or colloidal matter surface during river water migration. For the plant uptake, the root prefers to have ²⁶Mg, leading the plant itself rich in heavier Mg isotopic composition. In addition, formation of secondary minerals in rivers could also reflect the changes of chemical parameters in rivers (such as major elements, CO₂ solubility, pH, etc.). Hence, Mg isotopic composition in rivers and associated isotope fractionations are not only the basis for the application of magnesium isotope to trace surface material cycle, but also have important significance for the further understanding the geochemical cycle of magnesium isotopes.     

The origin of K-feldspar megacrysts hosted in alkaline potassic rocks from central Italy: a track for low-pressure processes in mafic magmas

In situ Sr-isotope and microchemical studies were used to determine the provenance of K-feldspar megacrysts hosted in mafic alkaline potassic, ultrapotassic rocks and in differentiated rocks from two nearby volcanic apparatus in central Italy.

At Monte Cimino volcanic complex, mafic leucite-free ultrapotassic megacryst-bearing rocks of olivine latitic composition are associated with evolved latite and trachyte. Here, latites and trachytes straddle the sub-alkaline field. Age-corrected ⁸⁷Sr/⁸⁶Sr values (Sr_i) of the analysed Cimino olivine latites vary from 0.71330 and 0.71578 and strongly increase at constant Mg value. Latite and trachyte have lower Sr_i than olivine latites ranging between 0.71331 and 0.71361. Sr_i of K-feldspar megacrysts from olivine latites are between 0.71352 and 0.71397, but core and rim ⁸⁷Sr/⁸⁶Sr ratios within individual megacryst are indistinguishable. In all the mafic rocks, the megacrysts are not in isotopic equilibrium with the hosts. K-feldspar megacrysts from both the latite and trachyte have similar Sr-isotope compositions (Sr_i=0.71357–0.71401) to those in the olivine latites. However, Sr_i of megacryst in the trachyte vary significantly from core to rim (Sr_i from 0.71401 to 0.71383). As with the olivine latites, the K-feldspar megacrysts are not in isotopic equilibrium with bulk rock compositions of the latite or trachyte.

At Vico volcano, megacryst-bearing rocks are mafic leucite-free potassic rocks, mafic leucite-bearing ultrapotassic rocks and old trachytic rocks. The mafic leucite-bearing and leucite-free rocks are a tephri-phonolite and an olivine latite, respectively. A megacryst in Vico trachyte is isotopically homogeneous (Sr_i CORE=0.71129, RIM=0.71128) and in equilibrium with the host rock (Sr_i bulk ROCK=0.71125). Sr_i of megacryst from tephri-phonolite is clearly not in isotopic equilibrium with its host (Sr_i bulk ROCK=0.71158), and it increases from core (Sr_i=0.71063) to rim (Sr_i=0.71077). A megacryst in Vico olivine latite is isotopically homogeneous (Sr_i CORE=0.71066, RIM=0.71065), but not in equilibrium with the host rock (Sr_i bulk ROCK=0.71013).

The Sr isotope microdrilling technique reveals that Cimino megacrysts were crystallised in a Cimino trachytic magma and were subsequently incorporated by mixing/mingling processes in the latitic and olivine latitic melts. A model invoking the presence of a mafic sub-alkaline magma, which was mixed with the olivine latite, is proposed to justify the lack of simple geochemical mixing relation between Cimino trachytes and olivine latites. This magmatological model is able to explain the geochemical characteristics of Cimino olivine latites, otherwise ascribed to mantle heterogeneity.

The similarity of core Sr_i of megacrysts hosted in Vico tephri-phonolite and olivine latite suggests that the K-feldspar megacrysts are co-genetic. Isotopic equilibrium between megacryst and Vico host trachyte indicates that the trachyte is the parent of this megacryst. On the contrary, the megacrysts hosted in tephri-phonolite and olivine latite do not derive from the old trachytic magma because no diffusion process may explain the core to rim Sr isotope increase of the xenocryst hosted in the tephri-phonolite. The megacrysts hosted in the Vico mafic rocks might derive from a trachytic melt similar in composition to the old Vico trachytes.     

Melting relations of peridotite and the density crossover in planetary mantles

Melting relations of primitive peridotite were studied up to 25 GPa. The change of the liquidus phase from olivine to majorite occurs at 16 GPa. We confirmed the density crossover of the FeO-rich peridotite melt and the equilibrium olivine (Fo₉₀) at 7 GPa. Sinking of equilibrium olivine (Fo₉₅) in the primitive peridotite melt was observed up to 10 GPa. The compression curves of FeO-rich peridotitic and komatiite melts reported in this and earlier work suggest that the density crossover in the Earth's mantle will be located at 11–12 GPa at 2000°C, consistent with an previous estimation by C.B. Agee and D. Walker.

The density crossover can play a key role in the Moon and the terrestrial planets, such as the Earth, Venus and Mars. Majorite and some fraction of melt could have separated from the ascending diapir and sunk downwards at the depths below the density crossover. This process could have produced a garnet-rich transition zone in the Earth's mantle. The density crossover may exist in the FeO-rich lunar mantle at around the center of the Moon. The density crossover which exists at the depth of 600 km in the Martian mantle plays a key role in producing a fractionated mantle, which is the source the parent magmas of the SNC meteorites.     

On the in situ aqueous alteration of soils on Mars

Early (>3 Gy) wetter climate conditions on Mars have been proposed, and it is thus likely that pedogenic processes have occurred there at some point in the past. Soil and rock chemistry of the Martian landing sites were evaluated to test the hypothesis that in situ aqueous alteration and downward movement of solutes have been among the processes that have transformed these portions of the Mars regolith. A geochemical mass balance shows that Martian soils at three landing sites have lost significant quantities of major rock-forming elements and have gained elements that are likely present as soluble ions. The loss of elements is interpreted to have occurred during an earlier stage(s) of weathering that may have been accompanied by the downward transport of weathering products, and the salts are interpreted to be emplaced later in a drier Mars history. Chemical differences exist among the sites, indicating regional differences in soil composition. Shallow soil profile excavations at Gusev crater are consistent with late stage downward migration of salts, implying the presence of small amounts of liquid water even in relatively recent Martian history. While the mechanisms for chemical weathering and salt additions on Mars remain unclear, the soil chemistry appears to record a decline in leaching efficiency. A deep sedimentary exposure at Endurance crater contains complex depth profiles of SO₄, Cl, and Br, trends generally consistent with downward aqueous transport accompanied by drying. While no model for the origin of Martian soils can be fully constrained with the currently available data, a pedogenic origin is consistent with observed Martian geology and geochemistry, and provides a testable hypothesis that can be evaluated with present and future data from the Mars surface.     

火星水成地貌研究进展

液态水在火星地表的塑造过程中起到了重要的作用,形成了峡谷网、外流河道、古湖泊以及三角洲和冲积扇等多种多样的水成地貌,它们一直是火星探测与研究的热点和焦点.本文对火星水成地貌的探测历史、地形地貌特征、时空分布等方面的研究进展进行总结,探讨水成地貌对火星气候演化及天体生物学研究的指示意义.在此基础上,提出当前火星水成地貌研究存在的问题,认为需要在火星水成地貌的水源类型、水成地貌所指示的火星水环境特征、亚马逊纪水成地貌的成因、火星水成地貌与我国柴达木盆地地貌的类比等方面开展进一步研究,为更深入的认识火星水成地貌,了解火星气候变化及宜居性提供支持.     

The behaviour of Li and Mg isotopes during primary phase dissolution and secondary mineral formation in basalt

This study presents lithium (Li) and magnesium (Mg) isotope data from experiments designed to assess the effects of dissolution of primary phases and the formation of secondary minerals during the weathering of basalt. Basalt glass and olivine dissolution experiments were performed in mixed through-flow reactors under controlled equilibrium conditions, at low pH (2-4) in order to keep solutions undersaturated (i.e. far-from equilibrium) and inhibit the formation of secondary minerals. Combined dissolution-precipitation experiments were performed at high pH (10 and 11) increasing the saturation state of the solutions (moving the system closer to equilibrium) and thereby promoting the formation of secondary minerals.At conditions far from equilibrium saturation state modelling and solution stoichiometry suggest that little secondary mineral formation has occurred. This is supported by the similarity of the dissolution rates of basalt glass and olivine obtained here compared to those of previous experiments. The δ⁷Li isotope composition of the experimental solution is indistinguishable from that of the initial basalt glass or olivine indicating that little fractionation has occurred. In contrast, the same experimental solutions have light Mg isotope compositions relative to the primary phases, and the solution becomes progressively lighter with time. In the absence of any evidence for secondary mineral formation the most likely explanation for these light Mg isotope compositions is that there has been preferential loss of light Mg during primary phase dissolution.For the experiments undertaken at close to equilibrium conditions the results of saturation state modelling and changes in solution chemistry suggest that secondary mineral formation has occurred. X-ray diffraction (XRD) measurements of the reacted mineral products from these experiments confirm that the principal secondary phase that has formed is chrysotile. Lithium isotope ratios of the experimental fluid become increasingly heavy with time, consistent with previous experimental work and natural data indicating that ⁶Li is preferentially incorporated into secondary minerals, leaving the solution enriched in ⁷Li. The behaviour of Mg isotopes is different from that anticipated or observed in natural systems. Similar to the far from equilibrium experiments initially light Mg is lost during olivine dissolution, but with time the δ²⁶Mg value of the solution becomes increasingly heavy. This suggests either preferential loss of light, and then heavy Mg from olivine, or that the secondary phase preferentially incorporates light Mg from solution. Assuming that the secondary phase is chrysotile, a Mg-silicate, the sense of Mg fractionation is opposite to that previously associated with silicate soils and implies that the fractionation of Mg isotopes during silicate precipitation may be mineral specific. If secondary silicates do preferentially remove light Mg from solution then this could be a possible mechanism for the relatively heavy δ²⁶Mg value of seawater. This study highlights the utility of experimental studies to quantify the effects of natural weathering reactions on the Li and Mg geochemical cycles.     

Freezing-resistant liquid water in porous media, a possible mechanism to account for the fluidized transport of sediments on Mars: an example from East Gorgonum crater

ABSTRACT A mudflow-like deposit resting on the bottom of the East Gorgonum Crater (Mars; 37.4°S, 168.0°W) may provide new insight regarding the debate on the existence of water over the Martian surface. Because water in a mudflow is confined to a porous medium, we analyse this case from the perspective of non-equilibrium systems. Fluids confined to porous media behave in a special way, the system being ruled by kinetic restrictions, which alter the expected thermodynamic equilibrium. These non-equilibrium conditions allow the existence of pure liquid water to temperatures as low as − 40 °C, and even less if the system includes brines. Thus, application of the triple point diagram of water on the Martian surface may constitute a simplistic approach if we are dealing with confined, and yet moving, water in the form of a mudflow. We further suggest that the V-shaped channels excavated alongside the mudflow may have been caused by water rejected by syneresis from the moving sediment. We finally indicate that the series of deeply entrenched channels and debris aprons that occur only in the northern half of the crater might be related to the regional slope, which decreases in altitude to the south.     

Silicate mineralogy of martian meteorites

Basalts and basaltic cumulates from Mars (delivered to Earth as meteorites) carry a record of the history of that planet - from accretion to initial differentiation and subsequent volcanism, up to recent times. We provide new microprobe data for plagioclase, olivine, and pyroxene from 19 of the martian meteorites that are representative of the six types of martian rocks. We also provide a comprehensive WDS map dataset for each sample studied, collected at a common magnification for easy comparison of composition and texture. The silicate data shows that plagioclase from each of the rock types shares similar trends in Ca-Na-K, and that K₂O/Na₂O wt% of plagioclase multiplied by the Al content of the bulk rock can be used to determine whether a rock is “enriched” or “depleted” in nature. Olivine data show that meteorite Y 980459 is a primitive melt from the martian mantle as its olivine crystals are in equilibrium with its bulk rock composition; all other olivine-bearing Shergottites have been affected by fractional crystallization. Pyroxene quadrilateral compositions can be used to isolate the type of melt from which the grains crystallized, and minor element concentrations in pyroxene can lend insight into parent melt compositions.In a comparative planetary mineralogy context, plagioclase from Mars is richer in Na than terrestrial and lunar plagioclase. The two most important factors contributing to this are the low activity of Al in martian melts and the resulting delayed nucleation of plagioclase in the crystallizing rock. Olivine from martian rocks shows distinct trends in Ni-Co and Cr systematics compared with olivine from Earth and Moon. The trends are due to several factors including oxygen fugacity, melt compositions and melt structures, properties which show variability among the planets. Finally, Fe-Mn ratios in both olivine and pyroxene can be used as a fingerprint of planetary parentage, where minerals show distinct planetary trends that may have been set at the time of planetary accretion.Although the silicate mineralogical data alone cannot support one specific model of martian magmatism over another, the data does support the basic igneous reservoirs proposed for Mars, and may also be used to constrain some aspects of specific petrogenetic models. Examples include enriched and depleted reservoirs that can be identified by plagioclase K, Na and Al composition, multivalent element partitioning in olivine and pyroxene (V, Cr) elucidates oxygen fugacity conditions of the reservoirs, and minor element concentrations (i.e., Cr in pyx) show that proposed fractional crystallization models linking Y 980459 to QUE 94201 will not work.     

Experimental study of radon production and transport in an analogue for the Martian regolith

The suggestion that radon could be used as a radioactive tracer of regolith-atmosphere exchanges and as a proxy for subsurface water on Mars, as well as its indirect detection in the Martian atmosphere by the rover Opportunity, have raised the need for a better characterization of its production process and transport efficiency in the Martian soil. More specifically, a proper estimation of radon exhalation rate on Mars requires its emanation factor and diffusion length to be determined. The dependence of the emanation factor as a function of pore water content (at 267 and 293 K) and the dependence of the adsorption coefficient on temperature, specific surface area and nature of the carrier gas (He, He + CO₂) have been measured on a Martian soil analogue (Hawaiian palagonitized volcanic ash, JSC Mars-1), whose radiometric analysis has been performed. An estimation of radon diffusion lengths on Mars is provided and is used to derive a global average emanation factor (2-6.5%) that accounts for the exhalation rate inferred from the ²¹⁰Po surface concentration detected on Martian dust and from the ²¹⁴Bi signal measured by the Mars Odyssey Gamma Ray Spectrometer. It is found to be much larger than emanation factors characterizing lunar samples, but lower than the emanation factor of the palagonite samples obtained under dry conditions. This result probably reflects different degrees of aqueous alteration and could indicate that the emanation factor is also affected by the current presence of pore water in the Martian soil. The rationale of the “radon method” as a technique to probe subsurface water on Mars, and its sensitivity to soil parameters are discussed. These experimental data are useful to perform more detailed studies of radon transport in the Martian atmosphere using Global Climate Models and to interpret neutron and gamma data from Mars Odyssey Gamma Ray Spectrometer.     

地外有机化合物

球粒陨石中的有机化合物起源于星际介质,是构成太阳星云的初始组分,并与其他物质一起吸积形成小行星和行星。在小行星内,有机质经历了不同程度的水蚀变和热变质作用。球粒陨石中的有机化合物尽管是非生命成因,但组成极为复杂,主要是类似于干酪根的大分子物质,以及少量可溶性有机物。大部分可溶有机分子也发现于地球生物圈,但前者可具有完全不同的H、C、N等同位素组成,这也是它们来源于地球之外的重要证据。星云中宇宙线和紫外线（UV）的辐射、小行星的热变质和水蚀变,是地外有机质演化的主要过程。球粒陨石中的有机质是地球生命起源的物质基础,是生命起源不可或缺的重要环节。同样重要的是,大量的火星探测表明,火星历史上有过满足生命存在的基本条件,而在火星陨石中还发现了一些生物活动相关的线索。未来很可能首先在火星上发现地外生命存在的证据。     

Microscale carbon isotope variability in ALH84001 carbonates and a discussion of possible formation environments

The carbonates in martian meteorite ALH84001 preserve a record of aqueous processes on Mars at 3.9 Ga, and have been suggested to contain signatures of ancient martian life. The conditions of the carbonate formation environment are critical for understanding possible evidence for life on Mars, the history of water on Mars, and the evolution of the martian atmosphere. Despite numerous studies of petrographic relationships, microscale oxygen isotope compositions, microscale chemical compositions, and other minerals associated with the carbonates, formation models remain relatively unconstrained. Microscale carbon isotope analyses of ALH84001 carbonates reveal variable δ¹³C values ranging from +27 to +64‰. The isotopic compositions are correlated with chemical composition and extent of crystallization such that the Mg-poor, early-formed carbonates are relatively ¹³C depleted and the Mg-rich, later forming carbonates, are ¹³C enriched. These data are inconsistent with many of the previously proposed environments for carbonate formation, and a new set of hypotheses are proposed. Specifically, two new models that account for the data involve low temperature (<100°C) aqueous processes: (1) the carbonates formed during mixing of two fluids derived from separate chemical and isotopic reservoirs; or (2) the carbonates formed from high pH fluids that are exposed to a CO₂-rich atmosphere and precipitate carbonate, similar to high pH springs on Earth.     

Experimental constraints on the parental liquid of the Chassigny meteorite: A possible link between the Chassigny meteorite and a Martian Gusev basalt

Most magmas proposed as parental to the Martian SNC meteorites are high in iron and low in alumina. Yet, experiments at low pressures on such liquids have not produced the cumulate or melt-inclusion assemblages seen in the chassignite meteorites. Therefore, elevated pressure experiments under anhydrous and hydrous (water-undersaturated) conditions were conducted on a high-Fe, low-Al liquid proposed to be parental to the Chassigny meteorite. These experiments failed to produce the most magnesian cumulate phases, as well as the olivine hosted kaersutite-bearing melt-inclusion assemblage, of the chassignites. These results suggest that the parental liquid to the chassignite meteorites is both more magnesium and aluminum-rich than the previously considered composition (A^∗; Johnson et al., 1991). The proposed composition is similar to the Martian Adirondack class Gusev basalt Humphrey and suggests a link between the Chassigny meteorite and rocks on the surface of Mars.     

Reconstruction of the exhumation path of the Alpe Arami'ql garnet-peridotite body from depths exceeding 160 km

Chemical disequilibrium exists between all phases of the Alpe Arami garnet-peridotite body (Ticino, Switzerland) which hampers the evaluation of P–T  conditions of origin, yet disequilibrium offers the inherent possibility to derive a P–T–t path for this mantle slice. We tried to tackle this problem by carrying out new mineral analyses and taking diffusion rates and bulk-rock compositional effects into consideration. Peak metamorphic conditions from mineral core compositions were estimated as 1120±50 °C/5±0.2 GPa. These values are significantly higher than previously published results and were determined from a combination of the O'Neill & Wood (1979) Fe/Mg garnet–olivine exchange thermometer and the Al-in-orthopyroxene barometer (Brey & Köhler, 1990), and are supported by the Ca/Cr ratios in garnet, which are in accord with these conditions. Details of the exhumation path were derived from (1) rim compositions of minerals that yield a first retrograde stage of 720±50 °C/2±0.25 GPa (2) a spinel lherzolite assemblage in narrow shear zones (tectonic phase F0', after Möckel, 1969) which documents a second retrograde stage at 500–600 °C/0.8–1.5 GPa. The Ca content in olivine (Köhler & Brey, 1989) can be used to evaluate further P–T  conditions along the retrograde path. We measured very low values (30–40  ppm Ca) in the cores of olivine and a remarkable increase towards the rim (120  ppm). The low core values may reflect an equilibrium stage during the main Alpine metamorphism. The increasing values towards the olivine rims probably represent a late-stage heating event. The initial cooling rates for the peridotite body are between 2700 and 5100 °C Ma⁻¹, depending on which diffusion data are used.     

The bulk composition of Mars

An accurate assessment of the bulk chemical composition of Mars is fundamental to understanding planetary accretion, differentiation, mantle evolution, the nature of the igneous parent rocks that were altered to produce sediments on Mars, and the initial concentrations of volatiles such as H, Cl and S, important constituents of the Martian surface. This paper reviews the three main approaches that have been used to estimate the bulk chemical composition of Mars: geochemical/cosmochemical, isotopic, and geophysical. The standard model is one developed by Wänke and Dreibus in a series of papers, which is based on compositions of Martian meteorites. Since their groundbreaking work, substantial amounts of data have become available to allow a reassessment of the composition of Mars from elemental data, including tests of the basic assumptions in the geochemical models. The results adjust some of the concentrations in the Wänke–Dreibus model, but in general confirm its accuracy. Bulk silicate Mars has roughly uniform depletion of moderately volatile elements such as K (0.6 × CI), and strong depletion of highly volatile elements (e.g., Tl). The highly volatile elements are within uncertainties uniformly depleted at about 0.06 CI abundances. The highly volatile chalcophile elements are likewise roughly uniformly depleted, but with more scatter, with normalized abundances of 0.03 CI. Bulk planetary H₂O is much higher than estimated previously: it appears to be slightly less than in Earth, but D/H is similar in Earth and Mars, indicating a common source of water-bearing material in the inner solar system. K/Th ranges from ∼3000 to ∼5000 among the terrestrial planets, a small range compared to CI chondrites (19,000). FeO varies throughout the inner solar system: ∼3 wt% in Mercury, 8 wt% in Earth and Venus, and 18 wt% in Mars. These differences can be produced by varying oxidation conditions, hence do not suggest the terrestrial planets were formed from fundamentally different materials. The broad chemical similarities among the terrestrial planets indicate substantial mixing throughout the inner solar system during planet formation, as suggested by dynamical models.     

Confined fluids and their role in pressure solution

The process of pressure solution is defined as the dissolution of materials under high stress at grain-to-grain contacts and precipitation at interfaces under low stress. The kinetics of this process are still poorly understood mainly because of the large timescales involved. In this research, the Surface Forces Apparatus (SFA) technique was coupled with an optical interference technique for in situ visualization of the nanoscale deformations and thickness changes. The SFA was used to measure the forces (or pressures) and distances between two solid surfaces pressed together with a thin film between them. Using the SFA, combined with geological observations, we are studying the short-range colloidal forces between surfaces of mica and silica at the nanoscale such as van der Waals, electrostatic, and hydration forces.

This study involves two cases, the symmetric case of mica in contact with mica and the asymmetric case of a quartz surface in contact with mica. Our results reveal highly subtle effects depending on the nature and concentration of the counterions present in the solution either of Na⁺, Ca²⁺, or mixtures of these ions, as well as on the pH. For the symmetric case, the equilibrium interactions of force F or pressure P versus fluid film thickness T have been measured between the mica surfaces across aqueous films in the thickness range from T = 25 Å down to contact separations around T = 0 Å, and depend on the solution conditions and applied lithostatic pressure. Measurements have also been made of the rates of diffusion of ions through such ultra-thin films and on the precipitation and growth of ionic crystallite layers on the surfaces. Our results show that the diffusion coefficient of hydrated sodium is two orders of magnitude lower than the diffusion of water into mica–mica cleavage and a factor of 40 lower than the coefficient of sodium ions in bulk water.

For the asymmetric case, the dissolution of the quartz surface was observed to be dependent on the interfacial fluid composition and pH, the externally applied ‘lithostatic’ pressure, and the type of crystalline structure exposed to the mica surface. Our experiments also show that there is an initial stage after fresh solution is added in which the spacing between the surfaces increases, however, the thickness started decreasing steadily after approximately 4 h of exposure independently of the crystallinity of the quartz surface. For a particular set of conditions, the process eventually slows down and reaches equilibrium after some time, but a further increase in pressure restarts the dissolution process. This is also true for the addition of fresh interfacial solution during the experiment after a period of thickness fluctuation. These results are consistent with the observation that pressure solution of quartz is greatly enhanced with the presence of mica.     

Properties of electrostatic aggregates and their possible presence on Mars

Experiments indicate that at the high wind velocities characteristic of portions of the Martian surface, sand-sized particles will break down to silt and clay, which will then inevitably form sand-sized aggregates. Basalt and olivine aggregates held together by electrostatics were produced in an eolian abrasion device and their mass properties studied. It was difficult to examine aggregates after formation, as they separate and reform with very little handling, since electrostatic binding forces are quite weak.It is shown that aggregates range from 60 to more than 600 μm in diameter, that they generally are spheroidal in shape and become more elongate with increasing size, and that they tend to be layered with the inner portions more tightly bound than outer layers. After about one-and-one-half years, some aggregates lose their charge which is replaced with moisture; the aggregates retain their original sizes and shapes. None of the properties of electrostatic aggregates so far investigated are incompatible with the presence of these materials on Mars.