ALBERT

Description / Table of Contents: At the time of the first printing (1996), interest in the element boron was growing rapidly. We felt that it was an opportune moment to ask investigators active in research on boron to review developments in their respective fields so that readers could learn what was-and wasn't-known about boron and its minerals, geochemistry and petrology. Since 1996, interest in boron has, if anything, increased, and continued demand for the Reviews in Mineralogy "boron bible" has motivated the Mineralogical Society of America to reprint the volume. Demand is reflected in citations, and according to ISI's Science Citation Index, the number of citations since publication to the volume is about 380, with some individual chapters having been cited as many as 44 times. In preparation for this printing, authors of 15 of the 19 original chapters have updated, corrected or added to their chapters within the constraints that no pages be added. Most addenda are bibliographies of literature published since 1996; a few also include summaries of significant findings. Addenda for each chapter follow the chapter, except for those for Chapters 1 and 2, which are merged onto pages 115-116 and 385. A table of new B-minerals since 1996 is given on p. 28, and many modifications were made to the table (p. 7-27) of B-minerals known prior to 1996 (corrections to formulae, mineral names, localities, etc.). Similar up-datings of Table 1 (p. 223) in Chapter 5 and numerous tables in Chapter 9 (p. 387) were undertaken, and Figure 15 in Chapter 11 (p. 619), which-embarrassingly-was missing from the first printing, has been supplied. Addenda to Chapter 13 are introduced on p. 744 and completed on p. 863 and 864. The following salient developments in research related to B are mentioned in the addenda: New minerals. Twenty-two boron minerals have been or are about to be described, and four more have been approved by the International Mineralogical Association, representing an increase of 10%, comparable to the increase in the number of all new minerals described during the same period (Anovitz and Grew, Chapter 1) Tourmaline group. In addition to four new tourmaline species, a new classification has been proposed. Another tourmaline, olenite, has been shown to contain substantial amounts of excess B in tetrahedral coordination, a finding that has revolutionized our view of tourmaline crystal chemistry (Werding and Schreyer, Chapter 3; references in addendum to Henry and Dutrow, Chapter 10). Boron isotopes. New techniques for measuring isotope ratios using secondary ion mass spectroscopy (SIMS) with the ion microprobe open up new opportunities for in situ analyses of individual grains and fluid inclusions (Hervig, Chapter 16). Boron isotopes have found applications in paleoceanography and thus add to the tools available for the study of past climates (Palmer and Swihart, Chapter 13). One of the major questions facing the use of hydrogeochemical models is whether or not they can be used with confidence to predict future evolution of groundwater systems. There is much controversy concerning the validity and uncertainties of non-reactive fluid flow systems. Adding chemical interaction to these flow models only confounds the problem. Although such models may accurately integrate the governing physical and chemical equations, many uncertainties are inherent in characterizing the natural system itself. These systems are inherently heterogeneous on a variety of scales rendering it impossible to know precisely the many details of the flow system and chemical composition of the host rock. Other properties of natural systems such as permeability and mineral surface area, to name just two, may never be known with any great precision, and in fact may be unknowable. Because of these uncertainties, it remains an open question as to what extent numerical models of groundwater flow and reactive transport wilI be useful in making accurate quantitative predictions. Nevertheless, reactive transport models should be able to predict the outcome for the particular representation of the porous medium used in the model. Finally, it should be mentioned that numerical models are often our only recourse to analyze such environmental problems as safe disposal of nuclear waste where predictions must be carried out over geologic time spans. Without such models it would be impossible to analyze such systems, because they involve times too long to perform laboratory experiments. The results of model calculations may affect important political decisions that must be made. Therefore, it is all the more important that models be applied and tested in diverse environments so that confidence and understanding of the limitations and strengths of model predictions are understood before irreversible decisions are made that could adversely affect generations to come.

Description / Table of Contents: Contents: Introduction and previous research. - Seismology and neotectonics. - The gravity field. - Pre-Tertiary stratigraphy. - Granites. - Pre-Tertiary volcanic rocks. - Tertiary stratigraphy. - Tertiary volcanicity. - Quaternary volcanicity. - Fuel resources: oil and gas. - Fuel resources: coal. - Metallic mineral resources. - Structure and structural history. - Tectonic evolution. - Appendix: Radiometric age data for Sumatra.

Description / Table of Contents: The publication of this volume occurs at the one-hundredth anniversary of 1905, which has been called the annus mirabilus because it was the year of a number of enormous scientific advances. Among them are four papers by Albert Einstein explaining (among other things) Brownian motion, the photoelectric effect, the special theory of relativity, and the equation E = mc2. Also of significance in 1905 was the first application of another major advance in physics, which dramatically changed the fields of Earth and planetary science. In March of 1905 (and published the following year), Ernest Rutherford presented the following in the Silliman Lectures at Yale: "The helium observed in the radioactive minerals is almost certainly due to its production from the radium and other radioactive substances contained therein. If the rate of production of helium from known weights of the different radioelements were experimentally known, it should thus be possible to determine the interval required for the production of the amount of helium observed in radioactive minerals, or, in other words, to determine the age of the mineral." Rutherford E (1906) Radioactive Transformations. Charles Scriber's Sons, NY Thus radioisotopic geochronology was born, almost immediately shattering centuries of speculative conjectures and estimates and laying the foundation for establishment of the geologic timescale, the age of the Earth and meteorites, and a quantitative understanding of the rates of processes ranging from nebular condensation to Quaternary glaciations. There is an important subplot to the historical development of radioisotopic dating over the last hundred years, which, ironically, arises directly from the subsequent history of the U-He dating method Rutherford described in 1905. Almost as soon as radioisotopic dating was invented, it was recognized that the U-He [or later the (U-Th)/He method], provided ages that were often far younger than those allowed by stratigraphic correlations or other techniques such as U/Pb dating. Clearly, as R.J. Strutt noted in 1910, He ages only provided "minimum values, because helium leaks out from the mineral, to what extent it is impossible to say" (Strutt, 1910, Proc Roy Soc Lond, Ser A 84:379-388). For several decades most attention was diverted to U/Pb and other techniques better suited to measurement of crystallization ages and establishment of the geologic timescale. Gradually it became clear that other radioisotopic systems such as K/Ar and later fission-track also provided ages that were clearly younger than formation ages. In 1910 it may have been impossible to say the extent to which He (or most other elements) leaked out of minerals, but eventually a growing understanding of thermally-activated diffusion and annealing began to shed light on the significance of such ages. The recognition that some systems can provide cooling, rather than formation, ages, was gradual and diachronous across radioisotopic systems. Most of the heavy lifting in this regard was accomplished by researchers working on the interpretation of K/Ar and fission-track ages. Ironically, Rutherfordπs He-based radioisotopic system was one of the last to be quantitatively interpreted as a thermochronometer, and has been added to K/Ar (including 40Ar/39Ar) and fission-track methods as important for constraining the medium- to low-temperature thermal histories of rocks and minerals. Thermochronology has had a slow and sometimes fitful maturation from what were once troubling age discrepancies and poorly-understood open-system behaviors, into a powerful branch of geochronology applied by Earth scientists from diverse fields. Cooling ages, coupled with quantitative understanding of crystal-scale kinetic phenomena and crustal- or landscape-scale interpretational models now provide an enormous range of insights into tectonics, geomorphology, and subjects of other fields. At the same time, blossoming of lower temperature thermochronometric approaches has inspired new perspectives into the detailed behavior of higher temperature systems that previously may have been primarily used for establishing formation ages. Increased recognition of the importance of thermal histories, combined with improved analytical precision, has motivated progress in understanding the thermochronologic behavior of U/Pb, Sm/Nd, Lu/Hf, and other systems in a wide range of minerals, filling out the temperature range accessible by thermochronologic approaches. Thus the maturation of low- and medium-temperature thermochronology has led to a fuller understanding of the significance of radioisotopic ages in general, and to one degree or another has permeated most of geochronology. Except in rare cases, the goal of thermochronology is not thermal histories themselves, but rather the geologic processes responsible for them. Thermochronometers are now routinely used for quantifying exhumation histories (tectonic or erosional), magmatism, or landscape evolution. As thermochronology has matured, so have model and interpretational approaches used to convert thermal histories into these more useful geologic histories. Low-temperature thermochronology has been especially important in this regard, as knowledge of thermal processes in the uppermost few kilometers of the crust require consideration of coupled interactions of tectonic, geodynamic, and surface processes. Exciting new developments in these fields in turn drive improved thermochronologic methods and innovative sampling approaches. The chapters This volume presents 22 chapters covering many of the important modern aspects of thermochronology. The coverage of the chapters ranges widely, including historical perspective, analytical techniques, kinetics and calibrations, modeling approaches, and interpretational methods. In general, the chapters focus on intermediate- to low-temperature thermochronometry, though some chapters cover higher temperature methods such as monazite U/Pb closure profiles, and the same theory and approaches used in low-temperature thermochronometry are generally applicable to higher temperature systems. The widely used low- to medium-temperature thermochronometric systems are reviewed in detail in these chapters, but while there are numerous chapters reviewing various aspects of the apatite (U-Th)/He system, there is no chapter singularly devoted to it, partly because of several previous reviews recently published on this topic. Chapter 1 by Reiners, Ehlers, and Zeitler provides a perspective on the history of thermochronology, comments on modern work in this field and general lessons on the potential for noise to be turned into signal. This chapter also provides a summary of the current challenges, unresolved issues, and most exciting prospects in the field. Much of the modern understanding of kinetic controls on apparent ages, thermal histories, and sampling approaches comes from decades of progress in fission-track dating, a method that remains as essential as ever, partly because of the power of track-length measurements and the depth of (at least empirical) understanding of the kinetics of track annealing. Tagami, Donelick and OπSullivan review the fundamentals of modern fission-track dating (Chapter 2). Two of the most commonly dated, well-understood, and powerful minerals dated by fission-track methods are apatite and zircon, and the specifics of modern methods for these systems and their kinetics are reviewed by Donelick, OπSullivan, and Ketcham (Chapter 3), and Tagami (Chapter 4). Although 40Ar/39Ar and (U-Th)/He dating methods followed somewhat different paths to their modern thermochronologic incarnations, they have many features in common, especially in the kinetics of diffusion and closure. Zeitler and Harrison review the concepts underlying both 40Ar/39Ar and (U-Th)/He methods (Chapter 5). Zircon was one of the first minerals dated by the (U-Th)/He method, but has only just begun to be used for thermochronometry of both bedrock and detrital samples, as reviewed by Reiners (Chapter 6). Continuous time-temperature paths from intracrystalline variations of radiogenic Ar proven perhaps the most powerful of all thermochronologic approaches, and an innovative analogous approach in He dating (4He/3He thermochronometry) is revealing remarkably powerful constraints on the extreme low temperature end of thermal histories, as reviewed by Shuster and Farley (Chapter 7). Thermochronology of detrital minerals provides unique constraints on the long-term evolution of orogens, sediment provenance, and depositional age constraints, to name a few. Bernet and Garver (Chapter 8) review the essentials of detrital zircon fission-track dating, one of the most venerable and robust of detrital thermochronometers, and in Chapter 9, Hodges, Ruhl, Wobus, and Pringle review the use of 40Ar/39Ar dating of detrital minerals, demonstrating the power of detrital muscovite ages in illuminating variations in exhumation rates in catchments over broad landscapes. (U-Th)/He thermochronometry presents several unique interpretational challenges besides new kinetics and low temperature sensitivity. One of these is long-alpha stopping distances, and its coupling with diffusion and U-Th zonation in age corrections. Dunai reviews modeling approaches to deal with these issues in interpreting low-temperature thermal histories (Chapter 10). Ketcham (Chapter 11) reviews the theory and calibration of both forward and inverse models of thermal histories from fission-track and (U-Th)/He data, and makes some important points about the interpretations of such models. Translating thermal histories into exhumational histories and their tectonic or geomorphic significance across a landscape requires quantitative understanding of the thermal structure of the crust and how it is perturbed, a review of which is presented by Ehlers (Chapter 12). Braun (Chapter 13) illustrates the power of low-temperature thermochronometry to constrain topographic evolution of landscapes over time, using PECUBE. Gallagher, Stephenson, Brown, Holmes, and Ballester present a novel method of inverse modeling of fission-track and (U-Th)/He data for thermal histories over landscapes (Chapter 14). Continuous time-temperature paths from closure profiles or their step-heating-derived equivalents are, to some degree, the holy grail of thermochronology. Harrison, Zeitler, Grove, and Lovera (Chapter 15) provide a review of the theory, measurement, and interpretation of continuous thermal histories at both intermediate and high temperatures, derived from both K-feldspar 40Ar/39Ar and monazite U/Pb dating. Extensional orogens provide a special challenge and opportunity for thermochronometry because tectonic exhumation by footwall unroofing often outstrips erosional exhumation, and often occurs at high rates. As Stockli shows (Chapter 16) thermochronology in these setting provides opportunities to measure rates of a number of important processes, as well as obtain a snapshot of crustal thermal structure and its imprint on thermochronometers with varying closure temperatures. Spotila (Chapter 17) reviews the use of thermochronology applied to tectonic geomorphology in a wide range of orogenic settings, introducing the concept of denudational maturity. Thermochronology has found great utility in economic geology, and newly developed approaches pose great potential in this area, and shown by McInnes, Evans, Fu, and Garwin in their review of the use and modeling of thermochronology of hydrothermal ore deposits (Chapter 18). The thermal histories of sedimentary basins are also critical to understanding thermal maturation of hydrocarbons, but are also critical for understanding basin formation, erosional histories of source regions, fluid flow, and climate change and other temporal signals preserved in sedimentary rocks. Armstrong (Chapter 19) reviews these issues and the use of thermochronology in deducing the thermal histories of sedimentary basins. Drawing on large datasets of bedrock apatite fission-track dates, Kohn, Gleadow, Brown, Gallagher, Lorencak, and Noble demonstrate the power of modeling, and, importantly, effectively visualizing, integrated thermotectonic and denudational histories over large regions (Chapter 20). Thermal histories of meteorites provide constraints on a wide range of fundamentally important processes, including nebular condensation and early solar-system metamorphic histories, and the dynamics of interplanetary collisions and shock metamorphism. Min reviews thermochronologic approaches to understanding meteorite thermal histories (Chapter 21), including new methods and approaches. Finally, the importance of robust models with which to interpret thermochronologic data is underscored by the review of the Software for Interpretation and Analysis of Thermochronologic Data (Chapter 22), summarized and compiled by Ehlers, for programs associated with the work of authors in this volume and others.

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. We begin with a review of analytical methods for measuring and calibrating water contents in nominally anhydrous minerals by George Rossman. While infrared spectroscopy is still the most sensitive and most convenient method for detecting water in minerals, it is not intrinsically quantitative but requires calibration by some other, independent analytical method, such as nuclear reaction analysis, hydrogen manometry, or SIMS. A particular advantage of infrared spectroscopy, however, is the fact that it does not only probe the concentration, but also the structure of hydrous species in a mineral and in many cases the precise location of a proton in a mineral structure can be worked out based on infrared spectra alone. The methods and principles behind this are reviewed by Eugen Libowitzky and Anton Beran, with many illustrative examples. Compared to infrared spectroscopy, NMR is much less used in studying hydrogen in minerals, mostly due to its lower sensitivity, the requirement of samples free of paramagnetic ions such as Fe2+ and because of the more complicated instrumentation required for NMR measurements. However, NMR could be very useful under some circumstances. It could detect any hydrogen species in a sample, including such species as H2 that would be invisible with infrared. Potential applications of NMR to the study of hydrogen in minerals are reviewed by Simon Kohn. While structural models of "water" in minerals have already been deduced from infrared spectra several decades ago, in recent years atomistic modeling has become a powerful tool for predicting potential sites for hydrogen in minerals. The review by Kate Wright gives an overview over both quantum mechanical methods and classical methods based on interatomic potentials. Joseph Smyth then summarizes the crystal chemistry of hydrogen in high-pressure silicate and oxide minerals. As a general rule, the incorporation of hydrogen is not controlled by the size of potential sites in the crystal lattice; rather, the protons will preferentially attach to oxygen atoms that are electrostatically underbonded, such as the non-silicate oxygen atoms in some high-pressure phases. Moreover, heterovalent substitutions, e.g., the substitution of Al3+ for Si4+, can have a major effect on the incorporation of hydrogen. 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. Given the dramatic developments in areas of research that were virtually non-existent at the time of the earlier reviews, major sections have been added here on sulfide mineral surface chemistry and reactivity, formation and transformation of metal-sulfur clusters and nanoparticles, modeling of hydrothermal precipitation, and on sulfides in biosystems. However, it should be emphasized that the growth in the literature on certain aspects of sulfide mineralogy over the past 20 years or so has been such that comprehensive coverage is not possible in a single volume. Thus, the general area of "sulfides in biosystems" is probably worthy of a volume in itself, and "environmental sulfide geochemistry" (including topics such as oxidative breakdown of sulfides) is another area where far more could have been written. In selecting areas for detailed coverage in this volume, we have been mindful of the existence of other relatively recent review volumes, including those in the RiMG series. It has also been our intention not to cover any aspects of the natural occurrence, textural or paragenetic relationships involving sulfides. This is published information that, although it may be supplemented by new observations, is likely to remain useful for a long period and largely not be superceded by later work. In the following chapters, the crystal structures, electrical and magnetic properties, spectroscopic studies, chemical bonding, thermochemistry, phase relations, solution chemistry, surface structure and chemistry, hydrothermal precipitation processes, sulfur isotope geochemistry and geobiology of metal sulfides are reviewed. Makovicky (Chapter 2) discusses the crystal structures and structural classification of sulfides and other chalcogenides (including the sulfosalts) in terms of the relationships between structural units. This very comprehensive survey, using a rather different and complementary approach to that used in previous review volumes, shows the great diversity of sulfide structures and the wealth of materials that remain to be characterized in detail. These materials include rare minerals, and synthetic sulfides that may represent as yet undescribed minerals. Pearce, Pattrick and Vaughan (Chapter 3) review the electrical and magnetic properties of sulfides, discussing the importance of this aspect of the sulfides to any understanding of their electronic structures (chemical bonding) and to applications ranging from geophysical prospecting and mineral extraction to geomagnetic and palaeomagnetic studies. Rapidly developing new areas of interest discussed include studies of the distinctive properties of sulfide nanoparticles. Wincott and Vaughan (Chapter 4) then outline the spectroscopic methods employed to study the crystal chemistry and electronic structures of sulfides. These range from UV-visible through infrared and Raman spectroscopies, to X-ray emission, photoemission and absorption, and to nuclear spectroscopies. Chemical bonding (electronic structure) in sulfides is the subject of the following chapter by Vaughan and Rosso (Chapter 5), a topic which draws on knowledge of electrical and magnetic properties and spectroscopic data as experimental input, as well as on a range of rapidly developing computational methods. Attention then turns to the thermochemistry of sulfides in a chapter by Sack and Ebel (Chapter 6) which is followed by discussion of phase equilibria at high temperatures in the review by Fleet (Chapter 7). Sulfides in aqueous systems, with emphasis on solution complexes and clusters, forms the subject matter of the chapter written by Rickard and Luther (Chapter 8). Sulfide mineral surfaces are the focus of the next two chapters, both by Rosso and Vaughan. The first of these chapters (Chapter 9) addresses characterization of the pristine sulfide surface, its structure and chemistry; the second (Chapter 10) concerns surface reactivity, including redox reactions, sorption phenomena, and the catalytic activity of sulfide surfaces. Reed and Palandri (Chapter 11) show in the next chapter how much can now be achieved in attempting to predict processes of sulfide precipitation in hydrothermal systems. The final chapters deal with two distinctive areas of sulfide mineralogy and geochemistry. Seal (Chapter 12) presents a comprehensive account of the theory and applications of sulfur isotope geochemistry; sulfur isotope fractionation can provide the key to understanding the natural processes of formation of sulfide deposits. In the final chapter, Posfai and Dunin-Borkowski (Chapter 13) review the rapidly developing area of sulfides in biosystems, discussing aspects of both sulfide mineral-microbe interactions and biomineralization processes involving sulfides.

Description / Table of Contents: Abstract The Himalaya mountains contain not only one of the largest concentrations of ice outside the polar regions, but contribute to the hydrological requirements of large populations spread over seven nations. The exceptionally high elevations of this low-latitude cryosphere presents a natural laboratory and archives to study climate–tectonics interactions as well as regional v. global climate influences. The existing base-level data on the Himalayan cryosphere are highly variable. Several climate fluctuations occurred during the late Quaternary (MIS1–MIS5, especially the last c. 100 ka), which led to the evolution of the Himalayan landscape. Detailed studies of these archives, along with those of the present cryosphere and related hydrosphere, are essential for understanding the controls on present and future hydrology of the glacial-fed mountain rivers. This volume, a follow-up of the XII International Symposium on Antarctic Earth Science, Goa (A SCAR symposium), provides new data from locales spread over the entire Himalaya region and from Tibet. It provides a glimpse of the late Quaternary cryosphere, as well as a discussion in the last section on sustainability in the context of geohazard mitigations as well as the hydrological budget.

Description / Table of Contents: Cover; Title; Copyright; Contents; List of Illustrations; Preface; PART ONE: What Has Controlled Earth's Climate?; CHAPTER ONE: Climate and Human History; PART TWO: Nature in Control; CHAPTER TWO: Slow Going for a Few Million Years; CHAPTER THREE: Linking Earth's Orbit to Its Climate; CHAPTER FOUR: Orbital Changes Control Ice-Age Cycles; CHAPTER FIVE: Orbital Changes Control Monsoon Cycles; CHAPTER SIX: Stirrings of Change; PART THREE: Humans Begin to Take Control; CHAPTER SEVEN: Early Agriculture and Civilization; CHAPTER EIGHT: Taking Control of Methane

Description / Table of Contents: CHAPTER NINE: Taking Control of CO[sub(2)]CHAPTER TEN: Have We Delayed a Glaciation?; CHAPTER ELEVEN: Challenges and Responses; PART FOUR: Disease Enters the Picture; CHAPTER TWELVE: But What about Those CO[sub(2)] "Wiggles"?; CHAPTER THIRTEEN: The Horsemen of the Apocalypse: Which One?; CHAPTER FOURTEEN: Pandemics, CO[sub(2)], and Climate; PART FIVE: Humans in Control; CHAPTER FIFTEEN: Greenhouse Warming: Tortoise and Hare; CHAPTER SIXTEEN: Future Warming: Large or Small?; CHAPTER SEVENTEEN: From the Past into the Distant Future; EPILOGUE; CHAPTER EIGHTEEN: Global-Change Science and Politics

Description / Table of Contents: CHAPTER NINETEEN: Consuming Earth's GiftsAfterword to the Princeton Science Library Edition; Bibliography; Figure Sources; Index; A; B; C; D; E; F; G; H; I; K; L; M; N; O; P; R; S; T; U; V; W; Y

Description / Table of Contents: The impact on climate from 200 years of industrial development is an everyday fact of life, but did humankind''s active involvement in climate change really begin with the industrial revolution, as commonly believed? Plows, Plagues, and Petroleum has sparked lively scientific debate since it was first published--arguing that humans have actually been changing the climate for some 8,000 years--as a result of the earlier discovery of agriculture. The ""Ruddiman Hypothesis"" will spark intense debate. We learn that the impact of farming on greenhouse-gas levels, thousands of years before the i

Description / Table of Contents: Derived from an undergraduate course taught by the author, this accessible book seeks to challenge and provoke readers by posing a series of topical questions concerning climate change and society. Topic summaries provide answers to technical, socio-economic and moral questions surrounding the deployment of climate science. These include how to build and test a climate model, whom and what is most at risk from climate change, and whether we should geoengineer the climate. Practical exercises and case studies provide deeper insights by taking readers through role-play activities and authentic climate change projects. Supporting materials, including notes for instructors and students, graphics, video-clips, games, and online resources, offer scope for further private study and group work. With a focus on applying climate science in practice, this book is ideal for students of geography, natural science, engineering and economics, as well as practitioners involved in the climate service industry

Description / Table of Contents: Historische Gärten sind als denkmalgeschützte Kulturgüter wertvolle Zeugnisse unserer Zivilisation. Wie lassen sie sich unter veränderten klimatischen Bedingungen bewahren? Anhand von vier historischen Gartenanlagen wird der natürliche, kulturelle und soziale Rahmen analysiert, in den die "Bilder" des Gartens eingeschrieben sind. Welche Handlungsoptionen bestehen jedoch, wenn Pflanzen oder Bäume den standörtlichen Gegebenheiten nicht mehr angepasst sind? Vertreter aus den Natur-, Geistes- und Sozialwissenschaften sowie der Gartendenkmalpflege stellen erstmals gemeinsam Lösungsstrategien für die Bewahrung historischer Gärten als Gesamtkunstwerke unter dem Vorzeichen des Klimawandels vor.

Description / Table of Contents: Die moderne Wissenschaft hat tiefgreifend unser Verständnis der Natur geprägt. In den letzten drei Jahrhunderten bildete diese Idee der Natur den Hintergrund all unseres Tuns. Aufgrund der ökologischen Folgen des menschlichen Handelns tritt die Natur jedoch heute aus dem Hintergrund auf die Bühne, wie Bruno Latour in seinem faszinierenden Buch zeigt. Die Luft, die Meere, die Gletscher, das Klima, die Böden, alles interagiert mit uns. Wir haben die Epoche der Geohistorie betreten, das Zeitalter des Anthropozäns – mit dem Risiko eines Krieges aller gegen alle. Die alte Natur verschwindet und weicht einem Wesen, das schwierig zu bestimmen ist. Es ist alles andere als stabil und besteht aus einer Reihe von Feedbackschleifen in ständiger Bewegung. Gaia ist sein Name. Latour argumentiert, dass die komplexe und mehrdeutige Gaia-Hypothese, wie sie von James Lovelock entwickelt wurde, ein idealer Weg ist, um die ethischen, politischen, theologischen und wissenschaftlichen Aspekte des nunmehr veralteten Begriffs der Natur zu entwirren. Er legt den Grundstein für eine zukünftige Zusammenarbeit zwischen Wissenschaftlern, Theologen, Aktivisten und Künstlern, während wir beginnen, mit dem neuen Klimaregime zu leben.

Description / Table of Contents: Contents: Isotopes in Water. - Isotopes in tree rings. Isotopes in bones and teeth. Isotopes in lake sediments. Isotopes in speleothems. Isotopes in marine sediments.

Description / Table of Contents: Contents: Introduction ; Part I: Paleoenvironmental Changes ; Part II: Cryospheric Changes ; Part III: Hydrological Changes ; Part IV: Ecological Changes ; Part V: Human Dimensions ; Synthesis

Description / Table of Contents: This volume contains the contributions presented at a short course held in Golden, Colorado, October 25-27, 1996 in conjunction with the Mineralogical Society of America's (MSA) Annual Meeting with the Geological Society of America in Denver, Colorado. The field of reactive transport within the Earth Sciences is a highly multidisciplinary area of research. The field encompasses a number of diverse disciplines including geochemistry, geology, physics, chemistry, hydrology, and engineering. The literature on the subject is similarly spread out as can be seen by a perusal of the bibliographies at the end of the chapters in this volume. Because these distinct disciplines have evolved largely independently of one another, their respective treatments of reactive transport in the Earth Sciences are based on different terminologies, assumptions, and levels of mathematical rigor. This volume and the short course which accompanies it, is an attempt to some extent bridge the gap between these different disciplines by bringing together authors and students from different backgrounds. A wide variety of geochemical processes including such diverse phenomena as the transport of radiogenic and toxic waste products, diagenesis, hydrothermal ore deposit formation, and metamorphism are the result of reactive transport in the subsurface. Such systems can be viewed as open bio-geochemical reactors where chemical change is driven by the interactions between migrating fluids, solid phases, and organisms. The evolution of these systems involves diverse processes including fluid flow, chemical reaction, and solute transport, each with differing characteristic time scales. This volume focuses on methods to describe the extent and consequences of reactive flow and transport in natural subsurface systems. Our ability to quantify reactive transport in natural systems has advanced dramatically over the past decade. Much of this advance is due to the exponential increase in computer computational power over the past generation-geochemical calculations that took years to perform in 1970 can be performed in seconds in 1996. Taking advantage of this increase of computational power, numerous comprehensive reactive transport models have been developed and applied to natural phenomena. These models can be used either qualitatively or qualitatively to provide insight into natural phenomena. Quantitative models force the investigator to validate or invalidate ideas by putting real numbers into an often vague hypothesis and thereby starting the thought process along a path that may result in acceptance, rejection, or modification of the original hypothesis. Used qualitatively, models provide. insight into the general features of a particular phenomenon, rather than specific details. One of the major questions facing the use of hydrogeochemical models is whether or not they can be used with confidence to predict future evolution of groundwater systems. There is much controversy concerning the validity and uncertainties of non-reactive fluid flow systems. Adding chemical interaction to these flow models only confounds the problem. Although such models may accurately integrate the governing physical and chemical equations, many uncertainties are inherent in characterizing the natural system itself. These systems are inherently heterogeneous on a variety of scales rendering it impossible to know precisely the many details of the flow system and chemical composition of the host rock. Other properties of natural systems such as permeability and mineral surface area, to name just two, may never be known with any great precision, and in fact may be unknowable. Because of these uncertainties, it remains an open question as to what extent numerical models of groundwater flow and reactive transport wilI be useful in making accurate quantitative predictions. Nevertheless, reactive transport models should be able to predict the outcome for the particular representation of the porous medium used in the model. Finally, it should be mentioned that numerical models are often our only recourse to analyze such environmental problems as safe disposal of nuclear waste where predictions must be carried out over geologic time spans. Without such models it would be impossible to analyze such systems, because they involve times too long to perform laboratory experiments. The results of model calculations may affect important political decisions that must be made. Therefore, it is all the more important that models be applied and tested in diverse environments so that confidence and understanding of the limitations and strengths of model predictions are understood before irreversible decisions are made that could adversely affect generations to come.

Description / Table of Contents: Teil 1: Globale Klimaprojektionen und regionale Projektionen für Deutschland und Europa -- Teil 2: Klimawandel in Deutschland: Regionale Besonderheiten und Extreme -- Teil 3: Auswirkungen des Klimawandels in Deutschland -- Teil 4: Übergreifende Risiken und Unsicherheiten -- Teil 5: Integrierte Strategien zur Anpassung an den Klimawandel

Description / Table of Contents: Erstmals trägt dieses nationale Assessment den Forschungsstand zum Klimawandel umfassend für alle Themenbereiche und gesellschaftlichen Sektoren zusammen. Womit müssen wir in Deutschland rechnen, welche Auswirkungen werden die Klimaveränderungen auf Wirtschaft und Gesellschaft haben, und wie können wir uns wappnen? 126 Autoren aus ganz Deutschland äußern sich zu Themen wie bereits beobachtete und zukünftige Veränderungen, Wetterkatastrophen und deren Folgen, den Projektionen für die Zukunft, den Risiken sowie möglichen Anpassungsstrategien. Die Autoren stellen in verständlicher Sprache den aktuellen Forschungsstand dar und veranschaulichen die wichtigsten Gedanken in Grafiken und Tabellen. Alle Texte wurden mehrfach wissenschaftlich begutachtet. Klimawandel in Deutschland ist die erste Gesamtschau zu dem Themenkomplex, benennt offene Fragestellungen und liefert eine Grundlage für Entscheidungen im Zusammenhang mit dem Klimawandel. Deutschland reiht sich damit ein in die Liste von Ländern wie die Vereinigten Staaten, Österreich und Großbritannien, in denen derartige Berichte bereits vorliegen. Die Herausgeber: Prof. Dr. Guy Brasseur und Prof. Dr. Daniela Jacob, ehemaliger Direktor und gegenwärtige Direktorin des Climate Center Germany/Helmholtz-Zentrum Geesthacht, und Susanne Schuck-Zöller, die auch die Projektleitung übernommen hat, werden bei diesem Buch unterstützt von einem Editorial Board, dem elf herausragende Wissenschaftler aus den wichtigsten Klimaforschungseinrichtungen in Deutschland angehören

Description / Table of Contents: With the ever increasing spatial resolution in the characterization of microstructures, textures and chemical as well as isotopic patterns and the continuously improving sensitivity and precision in mineral chemical and isotopic analysis, increasing evidence has emerged indicating that phase relations in rocks from high-temperature environments may be modified during exhumation and cooling and that the original equilibrium phase relations may not have been preserved or that equilibrium may never have been attained fully even at high temperatures. This volume accompanies an EMU School intended bring contemporary research on mineral reaction kinetics to the attention of young researchers and to put it into the context of recent developments in related disciplines. The school and the accompanying volume cannot give a comprehensive review of the current state of geomaterials research. Rather a selection of topics, methods and concepts, which the contributors deem currently most relevant and instructive, is presented. The aim is to provide a methodologically sound insight into the theoretical foundations of mineral reaction kinetics, to help students to become acquainted with contemporary methods in experimentation and analytical techniques, and to give worked examples that illustrate recent advances in geoscience based on an improved characterization and understanding of mineral and rock systems.

Description / Table of Contents: combines the latest in weather, climate and earth science to introduce students to the concepts and current issues of meteorology. Grounded in the scientific method, the new edition of this highly visual text shows students how to observe, calculate and synthesize information as budding scientists. Specific discussions center on severe weather systems like tornadoes and hurricanes, as well as everyday elements like wind, precipitation and the seasons. The MindTap course provides students with engaging features such as Concept Animations, a digital Study Guide, and summative EOC assessment. New assignable Case Study activities in each chapter allow students to apply their knowledge to real life studies and meteorological events.

Description / Table of Contents: In Materials Science, investigations aiming to prepare new types of molecular sieves (porous materials) have opened a productive field of research inspired by the crystal structures of minerals. These new molecular sieves are distinct from zeolites in that they have different kinds of polyhedra that build up their structures. Of particular interest are the new molecular sieves characterized by a mixed "octahedral"-tetrahedral framework (heteropolyhedral frameworks), instead of a purely tetrahedral framework as in zeolites. Heteropolyhedral compounds have been extensively studied since the early 1990's, with particular attention having been focused on titanosilicates, such as ETS-4 (synthetic analog of the mineral zorite) and ETS-10. However, titanosilicates are not the only representatives of novel microporous mineral phases. The search for "octahedral"-tetrahedral silicates was extended to metals other than titanium, for instance, the zirconosilicates with the preparation of synthetic counterparts of the minerals gaidonnayite, petarasite and umbite. Many microporous heteropolyhedral compounds containing metals such as Nb, V, Sn, Ca and lanthanides, have been reported and a wide number of distinct structural types (e.g., rhodesite-delhayelite and tobermorite) have been synthesized and structurally characterized. Moreover, the potential applications of these novel materials have been evaluated, particularly in the areas of catalysis, separation of molecular species, ion exchange and optical and magnetic properties. A comprehensive review of the mineralogical, structural, chemical and crystal-chemical studies carried on natural phases may be extremely useful to inspire and favor investigations on analogs or related synthetic materials. A similar synergy between mineralogists and materials scientists already occurred in the "classical" case of zeolites, in which the wide and deep structural and crystal-chemical knowledge accumulated in the study of the natural phases was extraordinarily useful to the chemists who are active in the field of molecular sieves. In particular, the structural investigation of the natural phases may be extremely rewarding and helpful in orienting the work of synthesis and in understanding the nature of the synthetic products, for the following reasons: Whereas rarely the crystalline synthetic products are suitable for single-crystal structural investigations, the natural counterparts are often well crystallized. Crystallization in nature occurs from chemical systems characterized by a wide compositional range, thus producing compounds with a very rich and variable crystal chemistry, which may provide precious information, suggesting possible substituting elements and addressing the synthetic work in a very productive way. The present volume follows a meeting on "Micro- and mesoporous mineral phases" (Rome, December 6-7, 2004) that was jointly organized by the Accademia Nazionale dei Lincei (ANL) and the International Union of Crystallography (IUCr) via its Commission on Inorganic and Mineral Structures (CIMS). The meeting was convened by Fausto Calderazzo, Giovanni Ferraris, Stefano Merlino and Annibale Mottana and financially supported by several other organizations representing both Mineralogy (e.g., the International Mineralogical Association and the European Mineralogical Union) and Crystallography (e.g., the European Crystallographic Association and the Italian Association of Crystallography). To participants, ANL staff, organizations, and, in general, all involved persons, our sincere acknowledgments; in particular, we are grateful to Annibale Mottana who was able to convince the ANL Academicians to schedule and support the meeting. This volume of the RiMG series highlights the present knowledge on micro- and mesoporous mineral phases, with focus on their crystal-chemical aspects, occurrence and porous activity in nature and experiments. As zeolites are the matter of numerous ad hoc meetings and books - including two volumes in this series - they do not specifically appear in the present volume. The phases of the sodalite and cancrinite-davyne groups, which mineralogists consider distinct from zeolites, are instead considered (in the order, chapter 7 by W. Depmeier and part of chapter 8 by E. Bonaccorsi and S. Merlino, respectively). The first two chapters of the volume cover general aspects of porous materials. This includes the application of the IUPAC nomenclature developed for ordered porous materials to non-zeolite mineral phases (L.B. McCusker, chapter 1) and the extension to heteropolyhedral structures of a topological description by using nodes representing the coordination polyhedra (S.V. Krivovichev, chapter 2). Chapters from 3 to 7 are dedicated to various groups of heteropolyhedral porous structures for which the authors emphasize some of the more general aspects according to their research specialization. G. Ferraris and A. Gula (chapter 3) put the emphasis on the modular aspects of well-known porous phases (such as sepiolite, palygorskite and rhodesite-related structures) as well as on heterophyllosilicates that may be not strictly porous phases (according to the definition given in chapter 1) but could be the starting basis for pillared materials. The porous mineral phases typical of hyperalkaline rocks (such as eudialytes and labuntsovites) are discussed by N.V. Chukanov and I.V. Pekov under their crystal-chemical (chapter 4) and minerogenetic (chapter 5) aspects showing the role of ion exchange during the geological evolution from primary to later phases, with experimental cation exchange data also being reported. J. Rocha and Z. Lin (chapter 6) emphasize how research on the synthesis of octahedral-pentahedral-tetrahedral framework silicates has been inspired and motivated by the many examples of such materials provided by nature; synthesis, structure and possible technological applications of a wide number of these materials are also described. Following chapters 7 and 8 - which besides the cancrinite-davyne group, presents the crystallographic features of the minerals in the tobermorite and gyrolite groups - M. Pasero (chapter 9) illustrates the topological and polysomatic aspects of the "tunnel oxides," a historical name applied to porous oxides related to MnO2, and reviews their main technological applications. The next two chapters (10 and 11) draw attention to "unexpected" porous materials like apatite and sulfides. T.J. White and his team (chapter 10) convincingly show that the apatite structure type displays porous properties, some of which are already exploited. Chapter 10 also contains two appendices that report crystal and synthesis data for hundreds of synthetic apatites, a number that demonstrates how wide the interest is for this class of compounds. E. Makovicky (chapter 11) analyzes the structures of natural and synthetic sulfides and selenides showing that, even if experimental work proving porous activity is practically still missing, several structure types display promising channels. Chapter 12, by M. Mellini, is the only one dedicated to mesoporous mineral phases - which are crystalline compounds with pores wider than 2 nm. Examples discussed are carbon nanotubes, fullerenes - which occur also in nature - chrysotile, opal and, moving from channels to cages, clathrates.