Impact-induced devolatilization and hydrogen isotopic fractionation of serpentine: implications for planetary accretion

The degree of impact-induced devolatilization of nonporous serpentine, porous serpentine, and deuterium-enriched serpentine was investigated using two independent experimental methods, the gas recovery method and the solid recovery method, yielding consistent results. The gas recovery method enables determination of the chemical and hydrogen isotopic composition of the recovered gases. Experiments on deuterium-enriched serpentine unambiguously identify the samples as the source of the recovered gases, as opposed to other possible contaminants. For shock pressures near incipient devolatilization (Pinitial = 5.0 GPa), the hydrogen isotopic composition of the evolved gas is similar to that of the starting material. For higher shock pressures the bulk evolved gas is significantly lower in deuterium than the starting material. There is also significant reduction of H2O to H2 in gases recovered at higher shock pressures, probably caused by reaction of evolved H2O with the metal gas recovery fixture. The hydrogen isotopic fractionation between the evolved gas and the residual solid indicates nonequilibrium, kinetic control of gas-solid isotopic ratios. In contrast, gaseous H2O-H2 isotopic fractionation suggests high temperature (800-1300 K) isotopic equilibrium between the gaseous species, indicating initiation of devolatilization at sites of greater than average energy deposition (i.e., shear bands). Impact-induced hydrogen isotopic fractionation of hydrous silicates during accretion can affect the distribution of hydrogen isotopes of planetary bodies during accretion, leaving the interiors enriched in deuterium. The significance of this process for planetary development depends on the models used for extrapolation of the observed isotopic fractionation to devolatilizations greater than those investigated experimentally and assumptions about timing and rates of protoatmosphere loss, frequency of multiple impacts, and rates of gas-solid or gas-melt isotopic re-equilibration. A simple model indicates that substantial planetary interior enrichments of D/H relative to that of the incident material can result from impact-induced hydrogen fractionation during accretion.     

Accretion, core formation, H and C evolution of the Earth and Mars

Recent understandings of planetary accretion have suggested that accumulation of a small number of large planetesimals dominates intermediate to final growth stages of the terrestrial planets, with impact velocity high enough to induce extensive melting of the planetesimal and target materials, resulting in formation of a large molten region in which gravitational segregation of silicate and metal, that is, core formation proceeds. In case of homogeneous accretion, volatiles contained in each planetesimal are likely subjected to partitioning among gas, silicate melt, and molten metallic iron at significantly high temperatures and pressures in such a massive molten region. Each phase would subsequently form the proto-atmosphere, -mantle, or-core, respectively. Such chemical reprocessing of H and C associated with core formation, which is followed by both degassing from mantle and atmospheric escape, may result in a diverse range of H₂O/CO₂ in planetary surface environments, which mainly depends on the H and C content relative to metallic iron in planetary building stones. This may explain inferred difference in volatile distribution between the Earth's (relatively H₂O-rich, CO₂-poor) and the martian (H₂O-poor, CO₂-rich) surface environments. Such volatile redistribution may be systematically described by using the retentivity of H₂O, ξ, defined as follows: ξ = 1 − ([CO]⁰ + 2[CH₄]⁰ + 2[C(gr)]⁰)/[H₂O]⁰, where [i]⁰ represents mol number of species i partitioned into non-metallic phases, that is, gas and silicate melt in impact-induced molten region. When ξ > 0.5, relatively H₂O-rich and CO₂-poor surface environment may eventually evolve, although a small portion of H₂O partitioned into the NON=metallic phases are possibly consumed by subsequent chemical reactions with reduced C-species with producing CO₂ and H₂. When ξ< 0.5, on the contrary, H₂O consumption by the above reactions and selective loss of H₂ to space may result in relative H₂O-depleted and CO₂-rich surface environment. Given the building stone composition by the two-component model by Ringwood (1977) and Wänke (1981), ξ is found to decrease with increasing the mixing fraction of the volatile-rich component: ξ > 0.5 for the mixing fraction smaller than about 15–20% and ξ < 0 for the mixing fraction larger than about 20–30%. This is not significantly dependent on temperature and pressure in molten region and H/C ratio in the building stone. The estimated mixing fraction of the volatile-rich component, about 10% for the Earth and 35% for Mars, is consistent with the observed difference in volatile distribution between the surfaces of both planets.     

FeO and H2O and the homogeneous accretion of the earth

We present new shock devolatilization recovery data for brucite (Mg(OH)₂) shocked to 13 and 23 GPa. These data combined with previous data for serpentine (Mg₃Si₂O₅(OH)₄) are used to constrain the minimum size terrestrial planet for which planetesimal infall will result in an impact-generated water atmosphere. Assuming a chondritic abundance of minerals including 3–6%, by mass water, in hydrous phyllosilicates, we carried out model calculations simulating the interaction of metallic iron with impact-released free water on the surface of the accreting Earth. We assume that the reaction of water with iron in the presence of enstatite is the prime source of the terrestrial FeO component of silicates and oxides. Lower and upper bounds on the terrestrial FeO budget are based on mantle FeO content and possible incorporation of FeO in the outer core. We demonstrate that the iron-water reaction would result in the absence of atmospheric/hydrospheric water, if homogeneous accretion is assumed. In order to obtain10²⁵g of atmospheric water by the end of accretion, slightly heterogeneous accretion with initially 36% by mass iron planetesimals, as compared to a homogeneous value of 34% is required. Such models yield final FeO budgets, which either require a higher FeO content of the mantle (17 wt.%) or oxygen as a light element in the outer core of the Earth.     

Meteorite paleomagnetism - From magnetic domains to planetary fields and core dynamos

Meteorites represent the earliest records of the evolution of the solar system, providing information on the conditions, processes and chronology for formation of first solids, planetesimals and differentiated bodies. Evidence on the nature of magnetic fields in the early solar system has been derived from chondritic meteorites. Chondrules, which are millimeter sized silicate spherules formed by rapid melting and cooling, have been shown to retain remanent magnetization records dating from the time of chondrule formation and accretion of planetesimals. Studies on different meteorite classes, including ordinary and carbonaceous chondrites, have however provided contrasting results with wide ranges for protoplanetary disk magnetic fields. Developments on instrumentation and techniques for rock magnetic and paleointensity analyses are allowing increased precision. Micromagnetic and an array of geochemical, petrographic and electronic microscopy analyses provide unprecedented resolution, characterizing rock magnetic properties at magnetic domain scales. We review studies on chondrules from the Allende meteorite that reveal relationships among hysteresis parameters and physical properties. Coercivity, remanent and saturation remanence parameters correlate with chondrule size and density; in turn related to internal chondrule structure, mineralogy and morphology. Compound, fragmented and rimmed chondrules show distinct hysteresis properties, related to mineral composition and microstructures. The remanent magnetization record and paleointensity estimates derived from the Allende and other chondrites support remanent acquisition under influence of internal magnetic fields within parent planetesimals. Results support that rapid differentiation following formation of calcium-aluminum inclusions and chondrules gave rise to differentiated planetesimals with iron cores, capable of generating and sustaining dynamo action for million year periods. The Allende chondrite may have derived from a partly differentiated planetesimal which sustained an internal magnetic field.     

Heterogeneous accretion,composition and core–mantle differentiation of the Earth

A model of core formation is presented that involves the Earth accreting heterogeneously through a series of impacts with smaller differentiated bodies. Each collision results in the impactor's metallic core reacting with a magma ocean before merging with the Earth's proto-core. The bulk compositions of accreting planetesimals are represented by average solar system abundances of non-volatile elements (i.e. CI-chondritic), with 22% enhancement of refractory elements and oxygen contents that are defined mainly by the Fe metal/FeO silicate ratio. Based on an anhydrous bulk chemistry, the compositions of coexisting core-forming metallic liquid and peridotitic silicate liquid are calculated by mass balance using experimentally-determined metal/silicate partition coefficients for the elements Fe, Si, O, Ni, Co, W, Nb, V, Ta and Cr. Oxygen fugacity is fixed by the partitioning of Fe between metal and silicate and depends on temperature, pressure and the oxygen content of the starting composition. Model parameters are determined by fitting the calculated mantle composition to the primitive mantle composition using least squares minimization. Models that involve homogeneous accretion or single-stage core formation do not provide acceptable fits. In the most successful models, involving 24 impacting bodies, the initial 60–70% (by mass) of the Earth accretes from highly-reduced material with the final 30–40% of accreted mass being more oxidised, which is consistent with results of dynamical accretion simulations. In order to obtain satisfactory fits for Ni, Co and W, it is required that the larger (and later) impactor cores fail to equilibrate completely before merging with the Earth's proto-core, as proposed previously on the basis of Hf-W isotopic studies. Estimated equilibration conditions may be consistent with magma oceans extending to the core–mantle boundary, thus making core formation extremely efficient. The model enables the compositional evolution of the Earth's mantle and core to be predicted throughout the course of accretion. The results are consistent with the late accretion of the Earth's water inventory, possibly with a late veneer after core formation was complete. Finally, the core is predicted to contain ~ 5 wt.% Ni, ~ 8 wt.% Si, ~ 2 wt.% S and ~ 0.5 wt.% O.     

Non-volatile vs volatile behaviours of halogens during the AD 79 plinian eruption of Mt. Vesuvius, Italy

Pre-eruptive conditions and degassing processes of the AD 79 plinian eruption of Mt. Vesuvius are constrained by systematic F and Cl measurements in melt inclusions and matrix glass of pumice clasts from a complete sequence of the pumice-fallout deposits. The entire ‘white pumice’ (WP) magma and the upper part of the ‘grey pumice’ (GP) magma were saturated relative to sub-critical fluids (a Cl-rich H₂O vapour phase and a brine), with a Cl melt content buffered at ~ 5300 ppm, and a mean H₂O content of ~ 5%. The majority of the GP magma was not fluid-saturated. From these results it can be estimated that the WP magma chamber had a low vertical extent (< 500 m) and was located at a depth of ~ 7.5 km while the GP magma reservoir was located just beneath the WP one, but its vertical extent cannot be constrained. This is approximately two times deeper than previous estimates. H₂O degassing during the WP eruption followed a typical closed-system evolution, whereas GP clasts followed a more complex degassing path. Contrary to H₂O, Cl was not efficiently degassed during the plinian phase of the eruption.

This study shows that F and Cl behave as incompatible elements in fluid-undersaturated phonolitic melts. H₂O saturation is necessary for a significant partitioning of Cl into the fluid phase. However, Cl cannot be extracted in significant quantity from phonolitic melts during rapid H₂O degassing, e.g. during plinian eruptions, due to kinetics effects. Halogen contents are better preserved in volcanic glass (melt inclusions or matrix glass) than H₂O, therefore the combined analysis of both volatile species is required for reliable determination of pre-eruptive conditions and syn-eruptive degassing processes in magmas stored at shallow depths.     

A new kind of primitive chondrite, Allan Hills 85085

Allan Hills 85085 is a chemically and mineralogically unique chondrite whose components have suffered little metamorphism or alteration. This chondrite is unique because it has fewer and smaller chondrules (4 wt. %; mean diameter 16 μm) than any other chondrite, more metallic Fe,Ni (36%) and lithic and mineral silicate fragments (56%), and a lower abundance of troilite (2%) and volatiles. Most chondrules are cryptocrystalline or glassy and are depleted in volatiles, some small chondrules are also very depleted in refractory lithophiles. Matrix lumps (4%) partly resemble CI and CM matrices and may be foreign to the parental asteroid. Despite these differences, the components of ALH 85085 have some features common to most type 2 and the least metamorphosed type 3 chondrites: metallic Fe,Ni grains that contain 0.1–1 wt.% Cr, Si and P; Fe/(Fe + Mg) values of olivines, pyroxenes and chondrules are concentrated in the range 1–6 at.% with a few percent in the range 7–30%; porphyritic chondrules are chondritic in composition (except for their low volatile abundances). Thus the components of ALH 85085 probably have similar origins to those of components in other chondrites, and their properties largely reflect nebular, not asteroidal, processes.The bulk composition of ALH 85085 fits none of the nine groups of chondrites: it is richer in Fe (1.4 × CI levels when normalized to Si) and poorer in Na and S (0.1–0.2 × CI) than other chondrites. Low volatile concentrations are due to a low matrix abundance and loss of volatiles during or prior to chondrule formation, not to volatile loss during metamorphism. Chondrule textures imply extensive heating of chondrule melts above the liquidus, consistent with loss of volatiles from small volumes of melt during chondrule formation. The small size of chondrules is partly due to extensive fragmentation by impacts, which may have occurred on the parent asteroid or in the solar nebula. Collisions between chondrule precursor aggregates in the nebula could also be responsible for the small sizes of chondrules.Assuming that ALH 85085 is a representative sample of an asteroid, its properties lend support to models for the origins of the Earth, eucrite parent body and volatile-poor iron meteorites that invoke chondritic planetesimals depleted in volatiles. The existence of ALH 85085 and Kakangari suggests that the nine chondrite groups may provide a remarkably poor sample of the primitive chondritic material from which the asteroids formed. Certain similarities between ALH 85085 and Bencubbin and Weatherford suggest that the latter two primitive meteorites may actually be chondrites with even higher metal abundances (50–60 wt.%) and very large, partly fragmented chondrules.     

On the origin of isolated olivine grains in type 2 carbonaceous chondrites

The origin of olivine grains isolated in the matrix of C2 carbonaceous chondrites is an important problem. If these grains are condensates from a solar nebular gas, they contain compositional, isotopic and physical features that further elucidate that process. If, however, they are grains released by the breakup of chondrules, then many important condensation features have been lost during the melting that took place to form chondrules.In evaluating these two possibilities, care must be taken to determine which inclusions in C2 meteorites are actual chondrules and which are aggregates of grains that have never undergone melting. The two main types of aggregates, pyroxene-rich and pyroxene-poor, are forty to fifty times more abundant than chondrules. Four scenarios are presented to account for the kinds of aggregates and isolated grains seen in the Murchison C2 meteorite. An analysis of these scenarios is made in light of olivine crystal morphology, comparison of composition of glass inclusions inside olivine grains with interstitial glass in true chondrules and size distributions of olivines, isolated, in aggregates and in chondrules.It is concluded that no scenario that includes a chondrule-making step can account for the observed population of isolated olivine grains. An origin by direct condensation, partial comminution, aggregation and accretion best accounts for the sizes and morphological features observed.     

The origin of the Earth

It is not possible to consider the formation of the Earth in isolation without reference to the formation of the rest of the solar system. A brief account is given of the current scientific consensus on that topic, explaining the origin of an inner solar system rocky planet depleted in most of the gaseous and icy components of the original solar nebula. Volatile element depletion occurred at a very early stage in the nebula, and was probably responsible for the formation of Jupiter before that of the inner planets. The Earth formed subsequently from accumulation of a hierarchy of planetesimals. Evidence of these remains in the ancient cratered surfaces and the obliquities (tilts) of most planets. Earth melting occurred during this process, as well as from the giant Moon-forming impact. The strange density and chemistry of the Moon are consistent with an origin from the mantle of the impactor. Core-mantle separation on the Earth was coeval with accretion. Some speculations are given on the origin of the hydrosphere.     

Composition and classification of clasts in the St. Mesmin LL chondrite breccia

Seven samples of the unique St. Mesmin meteorite have been analyzed by instrumental and radiochemical neutron activation analysis for Na, Ca, Sc, Cr, Mn, Fe, Co, Ni, Zn, Ga, Ge, Se, In, Sm, Yb, Ir and Au. St. Mesmin is unique in being the only ordinary chondrite known to contain an unmelted xenolith of another ordinary chondrite. Data for two host matrix samples and three light clasts are consistent with their classification as LL chondrite material. The composition of the large dark xenolith confirms earlier evidence that it is an H chondrite; volatile abundances are consistent with it being highly shocked, petrologic type-4 material. In an olivine microporphyry, siderophile abundances are mostly about 0.13 times LL abundances, an apparent indication of metal loss during the shock melting which produced the clast. As in other regolithic chondrites, the dark host has higher contents of highly volatile elements than do the light clasts. We suggest that this results from a combination of differences in intensity of preexisting metamorphism as well as a redistribution of volatiles during regolith gardening.The H-group xenolith in St. Mesmin is a relatively recent addition to the parent body (< 1.4 Ga ago), but it is argued that this does not require regolith activity at that time. Rather the view is supported that the regolith period occurred very early in the meteorite's history (&gsim;4.0 Ga ago) and may have been related to the growth of the parent body. The H-group fragment may be part of the projectile whose impact excavated the St. Mesmin meteoroid from the LL parent body.     

北半球中高纬度对流层顶转换层中O3/H2O 混合关系的结构形态

利用北半球40°N～50°N纬度带上HALOE实验测量的O₃和H₂O廓线资料,根据示踪成分O₃和H₂O空间分布的化学寿命以及输运特征时间常数等性质,在等熵坐标中构建了对流层顶附近及最低平流层300～390 K等熵面间,O₃/H₂O混合关系的结构形态和季节特征.结果表明: (1) 在对流层顶转换层的320～380 K等熵面间O₃混合比廓线的斜率具有空间转折"突变",而H₂O混合比廓线的斜率则出现空间渐变转折.在对流层顶附近O₃和H₂O的源分别是平流层与对流层,使O₃混合比和H₂O混合比在320～380 K等熵面的两侧显现出截然不同的垂直分布梯度.(2) 在对流层顶附近O₃/H₂O达到最小二乘意义上的最佳拟合时,两者参考关系的对流层支与平流层支呈现出非规则"L"结构形态的季节与季节内变化,其中对流层支的斜率为负,而平流层支的斜率可随季节出现正负变化.同时,由"L"形态的转角处可确定随季节变化的化学对流层顶(chemopause)特征.(3) 由O₃/H₂O混合关系反映出对流层不同区域空气携带的物质成分分别与平流层空气混合而形成混合层,而且可使混合层的混合线不恒定.混合层的表现在2003年、2005年1月和2003年4月的混合程度相当,混合的等熵厚度大约是30 K,即在320～350 K等熵面间.2005年11月的混合高度有所增高,进入平流层的H₂O混合比要比2003年和2005年1月的小,混合的等熵厚度大约为30 K,在330～360 K等熵面间.不同季节混合的等熵厚度变化较小,但高度可随季节而变化.O₃/H₂O混合关系的平流层支随季节的变化很明显,1月最低平流层空气脱水是引起平流层支季节变化的重要原因.     

The origin of organic matter in the Martian meteorite ALH84001.

Stable carbon isotope measurements of the organic matter associated with the carbonate globules and the bulk matrix material in the ALH84001 Martian meteorite indicate that two distinct sources are present in the sample. The delta 13C values for the organic matter associated with the carbonate globules averaged -26% and is attributed to terrestrial contamination. In contrast, the delta 13C values for the organic matter associated with the bulk matrix material yielded a value of -15%. The only common sources of carbon on the Earth that yield similar delta 13C values, other then some diagenetically altered marine carbonates, are C4 plants. A delta 13C value of -15%, on the other hand, is consistent with a kerogen-like component, the most ubiquitous form of organic matter found in carbonaceous chondrites such as the Murchison meteorite. Examination of the carbonate globules and bulk matrix material using laser desorption mass spectrometry (LDMS) indicates the presence of a high molecular weight organic component which appears to be extraterrestrial in origin, possibly derived from the exogenous delivery, of meteoritic or cometary debris to the surface of Mars.     

Noble gas systematics of the Réunion mantle plume source and the origin of primordial noble gases in Earth’s mantle

New noble gas data of ultramafic xenoliths from Réunion Island, Indian Ocean, further constrain the characteristics of primordial and radiogenic noble gases in Earth’s mantle plume reservoirs. The mantle source excess of nucleogenic ²¹Ne is significantly higher than for the Hawaiian and Icelandic plume reservoirs, similar to excess of radiogenic ⁴He. ⁴⁰Ar/³⁶Ar of the Réunion mantle source can be constrained to range between 8000 and 12 000, significant ¹²⁹Xe and fission Xe excess are present. Regarding the relative contribution of primordial and radiogenic rare gas nuclides, the Réunion mantle source is intermediate between Loihi- and MORB-type reservoirs. This confirms the compositional diversity of plume sources recognized in other radioisotope systematics. Another major result of this study is the identification of the same basic primordial component previously found for the Hawaiian and Icelandic mantle plumes and the MORB reservoir. It is a hybrid of solar-type He and Ne, and ‘atmosphere-like’ or ‘planetary’ Ar, Kr, Xe (Science 288 (2000) 1036). ²⁰Ne/²²Ne ratios extend to maximum values close to 12.5 (Ne-B), which is the typical signature of solar neon implanted as solar corpuscular radiation. This suggests that Earth’s solar-type noble gas inventory was acquired by small (less than km-sized) precursor planetesimals that were irradiated by an active early sun in the accretion disk after nebular gas dissipation, or, alternatively, that planetesimals incorporated constituents irradiated in transparent regions of the solar nebula. Previously, such an early irradiation scenario was suggested for carbonaceous chondrites which follow common volatile depletion trends in the sequence CI–CM–CV–Earth. In turn, CV chondrites closely match Earth’s mantle composition in ²⁰Ne/²²Ne, ³⁶Ar/²²Ne and ³⁶Ar/³⁸Ar. This indicates that mantle Ar could well be a planetary component inherited from precursor planetesimals. However, a corresponding conclusion for mantle Kr and Xe is less convincing yet, but this may be just due to the lack of appropriate ‘meteoritic’ building blocks matching terrestrial composition. Alternatively, heavy noble gases in Earth’s mantle could be due to admixing of severely fractionated air, but this effect must have affected all mantle sources to a very similar extent, e.g. by global subduction before the last homogenization of the mantle reservoirs.     

The possible effects of large 19th and 20th century volcanic eruptions on zonal and hemispheric surface temperatures

The contribution of volcanic material to the stratosphere from major eruptions within the last two centuries has been estimated using volcanological criteria, including eruption type, eruption column height, volume and duration of eruption, and composition and degree of fragmentation of magma. The chronology of major explosive volcanic eruptions is compared with a record of mean surface-temperature deviation (ΔT) for the same interval constructed from all available temperature data. The temperature records are divided into 6 latitudinal zones, allowing analysis for individual zones where temperature changes induced by aerosol perturbation might be intensified.We focus on the explosive volcanic events which by our estimates injected the most material into the stratosphere. These include Tambora 1815, Krakatau 1883, Santa Maria 1902, Katmai 1912 and Quizapu 1932. Such eruptions appear to have produced a consistent but small temperature decrease on the order of 0.2° to 0.5°C on a hemispheric scale for periods ranging from one to five years, although these changes are similar to background temperature variations. The maximum change in ΔT after some of these explosions appears to lag by up to three years in going from equatorial to polar latitudes.Somewhat smaller eruptions, e.g. Agung 1963 and possibly Cosiguina 1835, seem to have produced about the same perturbation in ΔT as the larger eruptions. This suggests either a limiting mechanism on loading of the aerosol layer after a volcanic eruption or, that the composition of injected material (i.e., the ratio of silicate “dust” to volatiles, and composition of the volatiles) may significantly effect stratospheric optical depth perturbation. Temperatures do not remain depressed for a longer period after a series of closely timed eruptions (e.g., the 1881–1889 or the 1902–1903 sequences) than after single events.     

Emplacement conditions of komatiite magmas from the 3.49 Ga Komati Formation, Barberton Greenstone Belt, South Africa

This paper provides new constraints on the crystallization conditions of the 3.49 Ga Barberton komatiites. The compositional evidence from igneous pyroxene in the olivine spinifex komatiite units indicates that the magma contained significant quantities of dissolved H₂O. Estimates are made from comparisons of the compositions of pyroxene preserved in Barberton komatiites with pyroxene produced in laboratory experiments at 0.1 MPa (1 bar) under anhydrous conditions and at 100 and 200 MPa (1 and 2 kbar) under H₂O-saturated conditions on an analog Barberton composition. Pyroxene thermobarometry on high-Ca clinopyroxene compositions from ten samples requires a range of minimum magmatic water contents of 6 wt.% or greater at the time of pyroxene crystallization and minimum emplacement pressures of 190 MPa (6 km depth). Since high-Ca pyroxene appears after 30% crystallization of olivine and spinel, the liquidus H₂O contents could be 4 to 6 wt.% H₂O. The liquidus temperature of the Barberton komatiite composition studied is between 1370 and 1400°C at 200 MPa under H₂O-saturated conditions. When compared to the temperature-depth regime of modern melt generation environments, the komatiite mantle source temperatures are 200°C higher than the hydrous mantle melting temperatures inferred in modern subduction zone environments and 100°C higher than mean mantle melting temperatures estimated at mid-ocean ridges. When compared to previous estimates of komatiite liquidus temperatures, melting under hydrous conditions occurs at temperatures that are 250°C lower than previous estimates for anhydrous komatiite. Mantle melting by near-fractional, adiabatic decompression takes place in a melting column that spans 38 km depth range under hydrous conditions. This depth interval for melting is only slightly greater than that observed in modern mid-ocean ridge environments. In contrast, anhydrous fractional melting models of komatiite occur over a larger depth range ( 130 km) and place the base of the melting column into the transition zone.     

Origin and thermal evolution of icy satellites

The paper reviews the problem of formation and evolution of the so-called regular satellites of the giant planets, and it consists of two parts: the first describes the possible origin of the satellites, the second studies their evolution, attempting to stress the relations of the present status of the satellites with their evolutionary history.The formation of regular satellite systems around giant planets is probably related to the formation of the central planet. Some characteristics of regular satellite systems are quite similar, and suggest a common origin in a disk present around the central body. This disk can originate through different mechanisms which we will describe, paying attention to the so-called accretion disk model, in which the satellite-forming material is captured. The disk phase links the formation of the primary body with the formation of satellites. The subsequent stages of the disk's evolution can lead first to the formation of intermediate size bodies, and through the collisional evolution of these bodies, to the birth of satellite embryos able to gravitationally capture smaller bodies.Given the scenario in which icy satellites may be formed by homogeneous accretion of planetesimals made of a mixtures of ice and silicates, if no melting occurs during accretion, the satellites have a homogeneous ice-rock composition. For the smaller satellites this homogeneous structure should not be substantially modified; only sporadic local events, such as large impacts, can modify the surface structure of the smaller satellites. For the larger satellites, if some degree of melting appears during accretion, a differentiation of the silicate part occurs, the amount of differentiation and hence the core size depending on the fraction of gravitational potential energy retained during the accumulation process. Melting and differentiation soon after the accretion, for the larger satellites, could also depend on the convective evolution in presence of phase transitions and generate an intermediate rock layer, considerably denser than the underlying, still homogeneous core, and unstable to overturning on a geologic time scale. Moreover the liquid water mantle could be a transient feature because the mantle would freeze over several hundred million years. For these large bodies the stable configuration is expected to be one consisting of a silicate core and a mantle of mixed rock and ice.     

The origins and concentrations of water,carbon, nitrogen and noble gases on Earth

The isotopic compositions of terrestrial hydrogen and nitrogen are clearly different from those of the nebular gas from which the solar system formed, and also differ from most of cometary values. Terrestrial N and H isotopic compositions are in the range of values characterizing primitive meteorites, which suggests that water, nitrogen, and other volatile elements on Earth originated from a cosmochemical reservoir that also sourced the parent bodies of primitive meteorites. Remnants of the proto-solar nebula (PSN) are still present in the mantle, presumably signing the sequestration of PSN gas at an early stage of planetary growth. The contribution of cometary volatiles appears limited to a few percents at most of the total volatile inventory of the Earth. The isotope signatures of H, N, Ne and Ar can be explained by mixing between two end-members of solar and chondritic compositions, respectively, and do not require isotopic fractionation during hydrodynamic escape of an early atmosphere.The terrestrial inventory of ⁴⁰Ar (produced by the decay of ⁴⁰K throughout the Earth's history) suggests that a significant fraction of radiogenic argon may be still trapped in the silicate Earth. By normalizing other volatile element abundances to this isotope, it is proposed that the Earth is not as volatile-poor as previously thought. Our planet may indeed contain up to ~ 3000 ppm water (preferred range: 1000–3000 ppm), and up to ~ 500 ppm C, both largely sequestrated in the solid Earth. This volatile content is equivalent to an ~ 2 (± 1) % contribution of carbonaceous chondrite (CI-CM) material to a dry proto-Earth, which is higher than the contribution of chondritic material advocated to account for the platinum group element budget of the mantle. Such a (relatively) high contribution of volatile-rich matter is consistent with the accretion of a few wet planetesimals during Earth accretion, as proposed by recent dynamical models.The abundance pattern of major volatile elements and of noble gases is also chondritic, with two notable exceptions. Nitrogen is depleted by one order of magnitude relative to water, carbon and most noble gases, which is consistent with either N retention in a mantle phase during magma generation, or trapping of N in the core. Xenon is also depleted by one order of magnitude, and enriched in heavy isotopes relative to chondritic or solar Xe (the so-called “xenon paradox”). This depletion and isotope fractionation might have taken place due to preferential ionization of xenon by UV light from the early Sun, either before Earth's formation on parent material, or during irradiation of the ancient atmosphere. The second possibility is consistent with a recent report of chondritic-like Xe in Archean sedimentary rocks that suggests that this process was still ongoing during the Archean eon (Pujol et al., 2011). If the depletion of Xe in the atmosphere was a long-term process that took place after the Earth-building events, then the amounts of atmospheric ¹²⁹Xe and ^131–136Xe, produced by the short-lived radioactivities of ¹²⁹I (T_1/2 = 16 Ma) and ²⁴⁴Pu (T_1/2 = 82 Ma), respectively, need to be corrected for subsequent loss. Doing so, the I–Pu–Xe age of the Earth becomes ≤ 50 Ma after start of solar system formation, instead of ~ 120 Ma as computed with the present-day atmospheric Xe inventory.     

Some clues to the history of the H-group chondrites

SEM, optical and chemical observations have been performed on 12 H3-6 chondrites, 9 of them being also studied by other groups. Morphological features of chondrules and crystals (growth steps) are shown; the significance of the finely crystallised troilite in Menow and Ambapur Nagla is discussed in the light of the discovery that the NiFe blebs associated with it are Ni-rich (50–60% Ni). Sulphur should have been mobilized without shock evidence possibly as a result of solar heating. Pre-chondritic relict material is recognized by anomalous or variable mineral compositions, and in some cases, by the presence of overgrowths on relict cores. After short notes on individual chondrites, a tentative history of H chondrites is proposed. The chondrule-forming episode is considered as a remelting of pre-existing material. The accretion would immediately follow this event for type 6 (around 1000°C), and would occur at progressively lower temperature for types 5 and 4. Type 3 would represent material coming from an extended source region, an hypothesis consistent with the broader range composition of the particles and with their cooling before accretion to much lower temperatures (below 350°C).     

Cloud Structure And Composition Of Jupiter's Atmosphere

The understanding of the composition and cloudstructure has advanced greatly in the last few yearsand in particular was greatly improved upon followingthe highly successful Pioneer and Voyager missions tothat planet. Recently the Galileo spacecraft has goneinto orbit about Jupiter and its remote sensinginstruments, including the Near Infrared MappingSpectrometer (NIMS) and the Solid State Imager (SSI),have yielded exciting new details of the spatial andvertical structure of the Jovian clouds and volatiles.At the same time Galileo's entry probe has made thefirst ever in situ measurements of conditions inthe atmosphere. Recent ground-based observations havealso added to the body of evidence from whichconditions in the Jovian atmosphere may be inferred.This paper aims to review the current understanding ofthe composition and cloud structure of Jupiter'satmosphere in the light of the new Galileo results andrecent ground-based, and earth-orbiting telescopeobservations.     

The Niger (I) carbonaceous chondrite and implications for the origin of aggregates and isolated olivine grains in C2 chondrites

The origin of olivine grains in C2 carbonaceous chondrites is a controversial topic: directly condensed material or detrital remnants of preexisting chondrules? This study shows that the Niger C2 meteorite is similar to Murchison but reveals several interesting features in relation to the origin of the olivine. Microprobe analysis of olivine (Si, Fe, Mg, Ca, Mn, Cr), glass and nickel-iron inclusions within the grains, and Fe-S-O phase as well as the relationships between the olivine grains in the aggregates, between the grains and the interstitial phyllosilicate matrix, between the inclusions and their host olivine grains, and the morphology of some aggregates all show that two populations of olivine coexist, probably crystallized from chondrule melts rather than by direct condensation from a solar nebula gas. The characteristics of the nickel-iron inclusions within the olivine suggest a magmatic chondrule-making stage from previously condensed materials.