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Partitioning of trivalent elements into olivine are used to explore basic issues relevant to igneous geochemistry, such as Henry's law. Additional information is contained in the original extended abstract.
Mafic igneous rocks probe the interiors of their parent objects, reflecting the compositions and mineralogies of their source regions, and the magmatic processes that engendered them. Incompatible trace element contents of mafic igneous rocks are widely used to constrain the petrologic evolution of planets. We focus on incompatible element ratios of martian meteorites to constrain the petrologic evolution of Mars in the context of magma ocean/cumulate overturn models [1]. Most martian meteorites contain some cumulus grains, but regardless, their incompatible element ratios are close to those of their parent magmas. Martian meteorites form two main petrologic/ age groupings; a 1.3 Ga group composed of clinopyroxenites (nakhlites) and dunites (chassignites), and a <1 Ga group composed of basalts and lherzolites (shergottites).
Papers published during the 1983-1986 period on the petrology and geochemistry of igneous rocks are discussed, with emphasis on tectonic environment. Consideration is given to oceanic rocks, subdivided into divergent margin suites (mid-ocean ridge basalts, ridge-related seamounts, and back-arc basin basalts) and intraplate suites (oceanic island basalts and nonridge seamounts), and to igneous rocks formed at convergent margins (island arc and continental arc suites), subdivided into volcanic associations and plutonic associations. Other rock groups discussed include continental flood basalts, layered mafic intrusions, continental alkalic associations, komatiites, ophiolites, ash-flow tuffs, anorthosites, and mantle xenoliths.
Is shergottite, nakhlite, and chassignite (SNC) meteorites are rocks propelled to earth by large meteoroid impacts on Mars, then it is possible to deduce much about Martian igneous petrology and geochemistry. Because SNCs are igneous rocks, however, it was not obvious that they could reveal much about sedimentary and soil petrology and low-temperature geochemistry of Mars. It is important, though, that at least four of eight SNCs carry evidence for low-temperature, extraterrestrial weathering product phases. Evidence is reviewed for Martian weathering and alteration products in SNCs and possible inferences for volatile/regolith interactions, regolith mineralogy, and sinks for the putative hidden volatiles on Mars are outlined.
The formation and earliest evolution of Mars involved core formation followed by magma ocean solidification and primordial crust formation. Here, we review the formation and early interior evolution of Mars as understood through meteorite studies. Martian meteorites exhibit ages that span the entire history of the Solar System, but most derive from compositionally distinct sources that formed early in the history of Mars. Geochemical and isotopic studies of Martian meteorites have provided critical information on Mars’ building blocks, bulk composition, and its differentiation into a core, mantle and crust. Radiogenic isotope systems provide vital insights into the petrogenesis of Martian meteorite source regions and into the nature and timescales of primordial differentiation on Mars. Application of short-lived isotope chronometers to Martian meteorites indicates that the Martian core formed early within <10 million years (Ma), while magma ocean differentiation and crust formation occurred soon thereafter, within the first tens of Ma of Solar System history. Bulk silicate Mars is variably depleted in moderately volatile elements relative to chondrites, but to a lesser extent than the Earth. The nature and evolution of more volatile elements and volatile species on Mars (e.g., H 2 O, C, S, halogens) remains an active area of investigation, but overall suggest that Mars is more enriched in volatile elements than the Moon but less than the Earth. While geochemical exploration of Mars coupled with new discoveries of Martian meteorites has provided a wealth of information, the compositional and lithologic diversity on Mars significantly exceeds that seen in the suites of Martian meteorites currently studied. This implies that our current perspective on the planet’s evolution is very likely biased, highlighting the need for future sample return missions to Mars.
This CD-ROM contains the abstracts and associated files for the Eleventh Annual V.M Goldschmidt Conference. Topics include: Organic Geochemistry; Metamorphic Processes; Igneous Processes; Stable and Radiogenic Isotopes; Planetary Geochemistry and Mineralogy; Mineralogy and Crystallography; Ore Deposits; and Aqueous Geochemistry.
Sedimentary rocks in Gale Crater on Mars indicate a varied provenance with a range of alteration and weathering [1, 2]. Geochemical trends identified in basaltic and alkalic sedimentary rocks by the Alpha Particle X-ray Spectrometer (APXS) on the Mars rover Curiosity represent a complex interplay of igneous, sedimentary, weathering, and alteration processes. Assessing the relative importance of these processes is challenging with unknown compositions for parent sediment sources and with the constraints provided by Curiosity's instruments. We therefore look to Mars analogues on Earth where higher-resolution analyses and geologic context can constrain interpretations of Gale Crater geochemical observations. We selected Maunakea (AKA Mauna Kea) and Kohala volcanoes, Hawai'i, for an analogue study because they are capped by post-shield transitional basalts and alkalic lavas (hawaiites, mugearites) with compositions similar to Gale Crater [1, 3]. Our aim was to characterize Hawaiian geochemical trends associated with igneous processes, sediment transport, weathering, and alteration. Here, we present initial results and discuss implications for selected trends observed by APXS in Gale Crater.
The properties of the earth's core are overviewed with emphasis on seismologically determined regions and pressures and seismologically measured density, elastic wave velocities, and gravitational acceleration. Attention is given to solid-state convection of the inner core, and it is noted that though seismological results do not conclusively prove that the inner core is convective, the occurrence and magnitude of seismic anisotropy are explained by the effects of solid-state convection. Igneous petrology and geochemistry of the inner core, a layer at the base of the mantle and contact metasomatism at the core-mantle boundary, and evolution of the core-mantle system are discussed. It is pointed out that high-pressure melting experiments indicate that the temperature of the core is ranging from 4500 to 6500 K, and a major implication of such high temperature is that the tectonics and convection of the mantle, as well as the resulting geological processes observed at the surface, are powered by heat from the core. As a result of the high temperatures, along with the compositional contrast between silicates and iron alloy, the core-mantle boundary is considered to be most chemically active region of the earth.
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The shergottite, nakhlite, and Chassigny (SNC) meteorites are inferred to be samples from the Martian surface, and so provide a wealth of information on Martian petrology and geochemistry. Because the SNCs are igneous rocks, it has not been obvious that they could reveal much about low-temperature geochemical processes and atmosphere surface interactions on Mars. However, five of the eight SNCs are known to contain low-temperature hydrous minerals and related phase of likely martian origin. Here, we review these martian weathering and alteration products in SNCs and outline possible implications for volatile/regolith interactions and regolith sinks for volatiles on Mars.
The present paper describes the compositional systematics of 381 particles analyzed from 14161, which was taken near the lunar module as part of the bulk sample. Attention is given to the distribution of lithologies, based on petrographic examination and compositions determined by INAA, and to implications of the compositions of polymict particles regarding igneous precursors and soil-forming processes. It was found that the most abundant particles are the impact-melt lithologies and regolith and fragmental breccias. The mean composition of the entire suite of 2-4-mm particles differs from that of the associated less-than-1-mm fines by having higher concentrations of incompatible trace elements and Na2O, and a lower concentration of CaO. There is a subset of regolith breccia particles and agglutinates in the 2-4-mm particles that have nearly identical compositions and Is/FeO similar to those of the less-than-1-mm fines. It is suggested that these particles are constructional products formed from the local regolith rather than comminuted fragments of ancient regolith breccias.
Mafic igneous rocks serve as probes of the interiors of their parent bodies - the compositions of the magmas contain an imprint of the source region composition and mineralogy, the melting and crystallization processes, and mixing and assimilation. Although complicated by their multifarious history, it is possible to constrain the petrologic evolution of an igneous province through compositional study of the rocks. Incompatible trace elements provide one means of doing this. I will use incompatible element ratios of martian meteorites to constrain the early petrologic evolution of Mars. Incompatible elements are strongly partitioned into the melt phase during igneous processes. The degree of incompatibility will differ depending on the mineral phases in equilibrium with the melt. Most martian meteorites contain some cumulus grains, but nevertheless, incompatible element ratios of bulk meteorites will be close to those of their parent magmas. ALH 84001 is an exception, and it will not be discussed. The martian meteorites will be considered in two groups; a 1.3 Ga group composed of the clinopyroxenites and dunite, and a younger group composed of all others.
Mafic igneous rocks serve as probes of the interiors of their parent bodies - the compositions of the magmas contain an imprint of the source region composition and mineralogy, the melting and crystallization processes, and mixing and assimilation. Although complicated by their multifarious history, it is possible to constrain the petrologic evolution of an igneous province through compositional study of the rocks. Incompatible trace elements provide one means of doing this. I will use incompatible element ratios of martian meteorites to constrain the early petrologic evolution of Mars. Incompatible elements are strongly partitioned into the melt phase during igneous processes. The degree of incompatibility will differ depending on the mineral phases in equilibrium with the melt. Most martian meteorites contain some cumulus grains, but nevertheless, incompatible element ratios of bulk meteorites will be close to those of their parent magmas. ALH 84001 is an exception, and it will not be discussed. The martian meteorites will be considered in two groups; a 1.3 Ga group composed of the clinopyroxenites and dunite, and a younger group composed of all others.
Ureilites are enigmatic achondrites that have some characteristics resulting from high temperature igneous processing, yet retain other characteristics inherited from the solar nebula. They are basalt-depleted ultramafic rocks containing 7-66 mg/g elemental C. They are rich in noble gases and display a correlation between mg# and Delta (17)O. This mishmash of properties has engendered various models for ureilite genesis, from those in which nebular processes dominate to those in which parent body igneous processes dominate. Characterization of new ureilites, especially of new subtypes, is an important part of attempts to unravel the history of the ureilite parent body or bodies. Here we report on the petrology and geochemistry of a suite of ureilites, mostly from Antarctica, and use these data to discuss ureilite petrogenesis. Additional information is included in the original extended abstract.
A recent Special Issue of the Energies Journal on Deep Borehole Disposal of Nuclear Waste has delivered a timely update on the science and technology of borehole disposal and the types of radioactive wastes it could potentially accommodate. The Special Issue papers discuss (i) circumstances under which a national waste management programme might wish to consider deep borehole disposal [1], (ii) a status report of deep borehole disposal options in Germany [2], (iii) the use of deep horizontal drill-holes in sedimentary, metamorphic or igneous rocks for disposal of spent nuclear fuel and high-level radioactive waste [3], (iv) the analysis of corrosion performance of engineered barrier systems [4], (v) a review of the potential cementing systems suitable for deep borehole disposal [5], (vi) the thermal evolution around heat-generating waste for a wide range of material properties and disposal configurations [6], (vii) a geochemical analysis of deep brines focussed on fluid-rock interactions [7], (viii) post-closure performance assessment calculations for deep borehole disposal of Cs/Sr capsules [8], and (ix) an example safety case for deep borehole disposal of nuclear wastes [9]. This paper provides an overview of the main findings from these publications and highlights some of the technological and scientific challenges that need to be overcome when developing a deep borehole disposal concept. (authors)
Papers are presented on lunar highlands and lunar geology, igneous processes on the moon, and achondrites. Also considered are the geology, geochemistry, and atmosphere of Venus and Mars. Other topics include comets, cosmic dust, and primitive nebular materials. Experimental and theoretical studies on impact cratering are discussed, along with geological and geochemical studies of impact products.
The anorthositic crust of the Moon is often used as the archtypical example of a primary planetary crust. The abundance and purity of anorthosite in the Apollo sample collection and remote sensing data are generally attributed to an early global magma ocean which produced widespread floating plagioclase cumulates (the ferroan anorthosites; FANs. Recent geochronology studies report evidence of young (less than 4.4 Ga) FAN ages, which suggest that either some may not be directly produced from the magma ocean or that the final solidification age of the magma ocean was younger than previous estimates. A greater diversity of anorthositic rocks have been identified among lunar meteorites as compared to returned lunar samples. Granted that these lithologies are often based on small clasts in lunar breccias and therefore may not represent their actual whole rock composition. Nevertheless, as suggested by the abundance of anorthositic clasts with Mg# [Mg/(Mg+Fe)] less than 0.80 and the difficulty of producing the extremely high plagioclase contents observed in Apollo samples and the remote sensing data, modification of the standard Lunar Magma Ocean (LMO) model may be in order. To ground truth mission science and to further test the LMO and other hypotheses for the formation of the lunar crust, additional coordinated petrology and geochronology studies of lunar anorthosites would be informative. Here we report new mineral chemistry and trace element geochemistry studies of thick sections of a composite of FAN-suite igneous clasts contained in the lunar breccia 64435 in order to assess the significance of this type of sample for petrogenetic studies of the Moon. This work follows recent isotopic studies of the lithologies in 64435 focusing on the same sample materials and expands on previous petrology studies who identified three lithologies in this sample and worked on thin sections.
The lunar samples from the Apollo 16 and 17 flights which were analyzed include soil, igneous rock, anorthositic gabbro, orange soil, subfloor basalt, and norite breccia. Up to 57 elements including majors, minors, rare earths and other trace elements were determined in the lunar samples. The analytical techniques used were spark source mass spectrometry and neutron activation analysis. The latter was done either instrumentally or with group radiochemical separations. The differences in abundances of the elements in lunar soils at the various sites are discussed. With regard to the major elements only Si is about the same at all the sites. A detailed analysis which was performed on a sample of the Allende meteorite is summarized.