ALBERT

Description / Table of Contents: The very successful orbital missions of the 1990's, Clementine and Lunar Prospector, provided key mineralogical, geochemical, and geophysical data sets that extended our view of the Moon beyond what we knew from Apollo and Luna exploration to a truly global perspective. These new data sets have been integrated with information gained from three preceding decades of study of lunar samples and older, less complete remotely sensed data sets. Although there have been no new lunar sample-return missions since Apollo and Luna, new samples are available in the form of meteorites, recognized to be pieces of the Moon. These, too, play a role in improved knowledge of the Moon and in helping to couple information obtained by remote sensing with information obtained from rock and soil samples. As we stand on the edge of a new era of lunar and planetary exploration, including new missions to the Moon, Mars, and other planets and moons, we find it essential to examine in depth how the wide variety of data sets obtained during the course of lunar exploration can be used together to better understand the formation of the Moon and how it evolved to its present state. Such an understanding holds important lessons for the new era of lunar exploration as well as the exploration of other planets in the Solar System. This will ultimately lead to better knowledge of how our own planet Earth - with its unique environment suitable for the origin and evolution of life - originated and changed with time. This book assesses the current state of knowledge of lunar geoscience, given the data sets provided by missions of the 1990's, and lists remaining key questions as well as new ones for future exploration to address. It documents how a planet or moon other than the world on which we live can be studied and understood in light of integrated suites of specific kinds of information. The Moon is the only body other than Earth for which we have material samples of known geologic context for study. This book seeks to show how the different kinds of information gained about the Moon relate to each other and also to learn from this experience, thus allowing more efficient planning for the exploration of other worlds.

Description / Table of Contents: Earth is a water planet. Oceans of liquid water dominate the surface processes of the planet. On the surface, water controls weathering as well as transport and deposition of sediments. Liquid water is necessary for life. In the interior, water fluxes melting and controls the solid-state viscosity of the convecting mantle and so controls volcanism and tectonics. Oceans cover more than 70% of the surface but make up only about 0.025% of the planet's mass. Hydrogen is the most abundant element in the cosmos, but in the bulk Earth, it is one of the most poorly constrained chemical compositional variables. Almost all of the nominally anhydrous minerals that compose the Earth's crust and mantle can incorporate measurable amounts of hydrogen. Because these are minerals that contain oxygen as the principal anion, the major incorporation mechanism is as hydroxyl, OH-, and the chemical component is equivalent to water, H2O. Although the hydrogen proton can be considered a monovalent cation, it does not occupy same structural position as a typical cation in a mineral structure, but rather forms a hydrogen bond with the oxygens on the edge of the coordination polyhedron. The amount incorporated is thus quite sensitive to pressure and the amount of H that can be incorporated in these phases generally increases with pressure and sometimes with temperature. Hydrogen solubility in nominally anhydrous minerals is thus much more sensitive to temperature and pressure than that of other elements. Because the mass of rock in the mantle is so large relative to ocean mass, the amount that is incorporated the nominally anhydrous phases of the interior may constitute the largest reservoir of water in the planet. Understanding the behavior and chemistry of hydrogen in minerals at the atomic scale is thus central to understanding the geology of the planet. There have been significant recent advances in the detection, measurement, and location of H in the nominally anhydrous silicate and oxide minerals that compose the planet. There have also been advances in experimental methods for measurement of H diffusion and the effects of H on the phase boundaries and physical properties whereby the presence of H in the interior may be inferred from seismic or other geophysical studies. It is the objective of this volume to consolidate these advances with reviews of recent research in the geochemistry and mineral physics of hydrogen in the principal mineral phases of the Earth's crust and mantle.

Description / Table of Contents: Medical Mineralogy and Geochemistry is an emergent, highly interdisciplinary field of study. The disciplines of mineralogy and geochemistry are integral components of cross-disciplinary investigations that aim to understand the interactions between geomaterials and humans as well as the normal and pathological formation of inorganic solid precipitates in vivo. Research strategies and methods include but are not limited to: stability and solubility studies of earth materials and biomaterials in biofluids or their proxies (i.e., equilibrium thermodynamic studies), kinetic studies of pertinent reactions under conditions relevant to the human body, molecular modeling studies, and geospatial and statistical studies aimed at evaluating environmental factors as causes for activating certain chronic diseases in genetically predisposed individuals or populations. Despite its importance, the area of Medical Mineralogy and Geochemistry has received limited attention by scientists, administrators, and the public. The objectives of this volume are to highlight some of the existing research opportunities and challenges, and to invigorate exchange of ideas between mineralogists and geochemists working on medical problems and medical scientists working on problems involving geomaterials and biominerals. Examples presented in this volume (Table of contents below) include the effects of inhaled dust particles in the lung (Huang et al. 2006; Schoonen et al. 2006), biomineralization of bones and teeth (Glimcher et al. 2006), the formation of kidney-stones, the calcification of arteries, the speciation exposure pathways and pathological effects of heavy metal contaminants (Reeder et al. 2006; Plumlee et al. 2006), the transport and fate of prions and pathological viruses in the environment (Schramm et al. 2006), the possible environmental-genetic link in the occurrence of neurodegenerative diseases (Perl and Moalem 2006), the design of biocompatible, bioactive ceramics for use as orthopaedic and dental implants and related tissue engineering applications (Cerruti and Sahai 2006) and the use of oxide-encapsulated living cells for the development of biosensors (Livage and Coradin 2006).

Description / Table of Contents: For over half a century neutron scattering has added valuable information about the structure of materials. Unlike X-rays that have quickly become a standard laboratory technique and are available to all modern researchers in physics, chemistry, materials and earth sciences, neutrons have been elusive and reserved for specialists. A primary reason is that neutron beams, at least so far, are only produced at large dedicated facilities with nuclear reactors and accelerators and access to those has been limited. Yet there are a substantial number of experiments that use neutron scattering. While earth science users are still a small minority, neutron scattering has nevertheless contributed valuable information on geological materials for well over half a century. Important applications have been in crystallography (e.g. atomic positions of hydrogen and Al-Si ordering in feldspars and zeolites, Mn-Fe-Ti distribution in oxides), magnetic structures, mineral physics at non-ambient conditions and investigations of anisotropy and residual strain in structural geology and rock mechanics. Applications range from structure determinations of large single crystals, to powder refinements and short-range order determination in amorphous materials. Zeolites, feldspars, magnetite, carbonates, ice, clathrates are just some of the minerals where knowledge has greatly been augmented by neutron scattering experiments. Yet relatively few researchers in earth sciences are taking advantage of the unique opportunities provided by modern neutron facilities. The goal of this volume, and the associated short course by the Mineralogical Society of America held December 7-9 in Emeryville/Berkeley CA, is to attract new users to this field and introduce them to the wide range of applications. As the following chapters will illustrate, neutron scattering offers unique opportunities to quantify properties of earth materials and processes. Focus of this volume is on scientific applications but issues of instrumental availabilities and methods of data processing are also covered to help scientists from such diverse fields as crystallography, mineral physics, geochemistry, rock mechanics, materials science, biomineralogy become familiar with neutron scattering. A few years ago European mineralogists spearheaded a similar initiative that resulted in a special issue of the European Journal of Mineralogy (Volume 14, 2002). Since then the field has much advanced and a review volume that is widely available is highly desirable. At present there is really no easy access for earth scientists to this field and a more focused treatise can complement Bacon's (1955) book, now in its third edition, which is still a classic. The purpose of this volume is to provide an introduction for those not yet familiar with neutrons by describing basic features of neutrons and their interaction with matter as well illustrating important applications. The volume is divided into 17 Chapters. The first two chapters introduce properties of neutrons and neutron facilities, setting the stage for applications. Some applications rely on single crystals (Chapter 3) but mostly powders (Chapters 4-5) and bulk polycrystals (Chapters 15-16) are analyzed, at ambient conditions as well as low and high temperature and high pressure (Chapters 7-9). Characterization of magnetic structures remains a core application of neutron scattering (Chapter 6). The analysis of neutron data is not trivial and crystallographic methods have been modified to take account of the complexities, such as the Rietveld technique (Chapter 4) and the pair distribution function (Chapter 11). Information is not only obtained about solids but about liquids, melts and aqueous solutions as well (Chapters 11-13). In fact this field, approached with inelastic scattering (Chapter 10) and small angle scattering (Chapter 13) is opening unprecedented opportunities for earth sciences. Small angle scattering also contributes information about microstructures (Chapter 14). Neutron diffraction has become a favorite method to quantify residual stresses in deformed materials (Chapter 16) as well as preferred orientation patterns (Chapter 15). The volume concludes with a short introduction into neutron tomography and radiography that may well emerge as a principal application of neutron scattering in the future (Chapter 17).

Description / Table of Contents: The importance of sulfide minerals in ores has long been, and continues to be, a major reason for the interest of mineralogists and geochemists in these materials. Determining the fundamental chemistry of sulfides is key to understanding their conditions of formation and, hence, the geological processes by which certain ore deposits have formed. This, in turn, may inform the strategies used in exploration for such deposits and their subsequent exploitation. In this context, knowledge of structures, stabilities, phase relations and transformations, together with the relevant thermodynamic and kinetic data, is critical. As with many geochemical systems, much can also be learned from isotopic studies. The practical contributions of mineralogists and geochemists to sulfide studies extend beyond areas related to geological applications. The mining of sulfide ores, to satisfy ever increasing world demand for metals, now involves extracting very large volumes of rock that contains a few percent at most (and commonly less than one percent) of the metal being mined. This is true of relatively low value metals such as copper; for the precious metals commonly occurring as sulfides, or associated with them, the mineable concentrations (grades) are very much lower. The "as-mined" ores therefore require extensive processing in order to produce a concentrate with a much higher percentage content of the metal being extracted. Such mineral processing (beneficiation) involves crushing and grinding of the ores to a very fine grain size in order to liberate the valuable metal-bearing (sulfide) minerals which can then be concentrated. In some cases, the metalliferous (sulfide) minerals may have specific electrical or magnetic properties that can be exploited to enable separation and, hence, concentration. More commonly, froth flotation is used, whereby the surfaces of particles of a particular mineral phase are rendered water repellent by the addition of chemical reagents and hence are attracted to air bubbles pulsed through a mineral particle-water-reagent pulp. An understanding of the surface chemistry and surface reactivity of sulfide minerals is central to this major industrial process and, of course, knowledge of electrical and magnetic properties is very important in cases where those particular properties can be utilized. In the years since the publication of the first ever Reviews in Mineralogy volume (1974, at that time called MSA "Short Course Notes") which was entitled Sulfide Mineralogy, sulfides have become a focus of research interest for reasons centering on at least two other areas in addition to their key role in ore deposit studies and mineral processing technology. It is in these two new areas that much of the research on sulfides has been concentrated in recent years. The first of these areas relates to the capacity of sulfides to react with natural waters and acidify them; the resulting Acid Rock Drainage (ARD), or Acid Mine Drainage (AMD) where the sulfides are the waste products of mining, has the capacity to damage or destroy vegetation, fish and other aquatic life forms. These acid waters may also accelerate the dissolution of associated minerals containing potentially toxic elements (e.g., As, Pb, Cd, Hg, etc.) and these may, in turn, cause environmental damage. The much greater public awareness of the need to prevent or control AMD and toxic metal pollution has led to regulation and legislation in many parts of the world, and to the funding of research programs aimed at a greater understanding of the factors controlling the breakdown of sulfide minerals. The second reason for even greater research interest in sulfide minerals arose initially from the discoveries of active hydrothermal systems in the deep oceans. The presence of life forms that have chemical rather than photosynthetic metabolisms, and that occur in association with newly-forming sulfides, has encouraged research on the potential of sulfide surfaces in catalyzing the reactions leading to assembling of the complex molecules needed for life on Earth. These developments have been associated with a great upsurge of interest in the interactions between microbes and minerals, and in the role that minerals can play in biological systems. In the rapidly growing field of geomicrobiology, metal sulfides are of major interest. This interest is related to a variety of processes including, for example, those where bacteria interact with sulfides as part of their metabolic activity and cause chemical changes such as oxidation or reduction, or those in which biogenic sulfide minerals perform a specific function, such as that of navigation in magnetotactic bacteria. The development of research in areas such as geomicrobiology and environmental mineralogy and geochemistry, is also leading to a greater appreciation of the role of sulfides (particularly the iron sulfides) in the geochemical cycling of the elements at or near the surface of the Earth. For example, the iron sulfides precipitated in the reducing environments beneath the surface of modern sediments in many estuarine areas may play a key role in the trapping of toxic metals and other pollutants. In our understanding of "Earth Systems," geochemical processes involving metal sulfides are an important part of the story. The main objective of the present text is to provide an up-to-date review of sulfide mineralogy and geochemistry. The emphasis is, therefore, on such topics as crystal structure and classification, electrical and magnetic properties, spectroscopic studies, chemical bonding, high and low temperature phase relations, thermochemistry, and stable isotope systematics. In the context of this book, emphasis is on metal sulfides sensu stricto where only the compounds of sulfur with one or more metals are considered. Where it is appropriate for comparison, there is brief discussion of the selenide or telluride analogs of the metal sulfides. When discussing crystal structures and structural relationships, the sulfosalt minerals as well as the sulfides are considered in some detail (see Chapter 2; also for definition of the term "sulfosalt"). However, in other chapters there is only limited discussion of sulfosalts, in part because there is little information available beyond knowledge of chemical composition and crystal structure.