ALBERT

Description / Table of Contents: Contents: Chapter 1. Metabolic Synthesis Chapter 2. Chemical Biomarker Applications to Ecology and Paleoecology Chapter 3. Stable Isotopes and Radiocarbon Chapter 4. Analytical Chemical Methods and Instrumentation Chapter 5. Carbohydrates: Neutral and Minor Sugars Chapter 6. Proteins: Amino Acids and Amines Chapter 7. Nucleic Acids and Molecular Tools Chapter 8. Lipids: Fatty Acids Chapter 9. Isoprenoid Lipids: Steroids, Hopanoids, and Triterpenoids Chapter 10. Lipids: Hydrocarbons Chapter 11. Lipids: Alkenones, Polar Lipids, and Ether Lipids Chapter 12. Photosynthetic Pigments: Chlorophylls, Carotenoids, and Phycobilins Chapter 13. Lignins, Cutins, and Suberins Chapter 14. Anthropogenic Markers Appendix I. Atomic Weights of Elements Appendix II. Useful SI Units and Conversion Factors Appendix III. Physical and Chemical Constants Glossary Bibliography

Description / Table of Contents: Stable Isotope Geochemistry is an introduction to the use of stable isotopes in the geosciences. It is subdivided into three parts: theoretical and experimental principles; fractionation processes of light and heavy elements; the natural variations of geologically important reservoirs. Since the application of stable isotopes to earth sciences has grown in the last few years, a new edition appears necessary. Recent progress in analysing the rare isotopes of certain elements for instance allow the distinction between mass-dependent and mass-independent fractionations. Special emphasis has been given to the growing field of heavy elements. Many new references have been added, which will enable quick access to recent literature. For students and scientists alike the book will be a primary source of information with regard to how and where stable isotopes can be used to solve geological problems.

Description / Table of Contents: Until only a few years ago, I would never have imagined that a volume on the stable isotope geochemistry of elements like Mg, Fe or Cu would be written. In fact, a comic book of blank pages entitled The Stable Isotope Geochemistry of Fluorine would have been a more likely prospect. In volume 16 of this series, published in 1986, I wrote: Isotopic variations have been looked for but not found for heavy elements like Cu, Sn, and Fe .... Natural variations in isotopic ratios of terrestrial materials have been reported for other light elements like Mg and K, but such variations usually turn out to be laboratory artifacts. I am about ready to eat those words. We have known for many years that large isotopic fractionations of heavy elements like Pb develop in the source regions of TIMS machines. Nonetheless, most of us held fast to the conventional wisdom that no significant mass-dependent isotopic fractionations were likely to occur in natural or laboratory systems for elements that are either heavy or engaged in bonds with a dominant ionic character. With the relatively recent appearance of new instrumentation like MC-ICP-MS and heroic methods development in TIMS analyses, it became possible to make very precise measurements of the isotopic ratios of some of these non-traditional elements, particularly if they comprise three or more isotopes. It was eminently reasonable to reexamine these systems in this new light. Perhaps atomic weights could be refined, or maybe there were some unexpected isotopic variations to discover. There were around the turn of the present century, reports began appearing of biological fractionations of about 2-3 per mil for heavy elements like Fe and Cr and attempts were made to determine the magnitude of equilibrium isotope effects in these systems, both by experiment and semi-empirical calculations. Interest emerged in applying these effects to the study of environmental problems. Even the most recalcitrant skeptic now accepts the fact that measurable and meaningful variations in the isotopic ratios of heavy elements occur as a result of chemical, biological and physical processes. Most of the work discussed in this volume was published after the year 2000 and thus the chapters are more like progress reports rather than reviews. Skepticism now focuses on whether isotopic variations as small as 0.1 per mil are indeed as meaningful as some think, and the fact that measured isotopic fractionations of these non-traditional elements are frequently much smaller than predicted from theoretical considerations. In fact the large fractionations suggested by the calculations provide much of the stimulus for working in this discipline. Clearly some carefully designed experiments could shed light on some of the ambiguity. My optimism for the future of this burgeoning new field remains high because it is in very good hands indeed. Approximately three-quarters of the elements in the Periodic Table have two or more isotopes. RiM 16 and RiMG 43 were devoted to H, C, 0, and S isotope variations, and B isotope variations were discussed in RiM 33. The importance of these elements to geochemistry may be illustrated by a GeoRef search of 0 isotope publications, which yields over 25,000 papers, theses, and abstracts spanning over five decades. Isotopic variations of the remaining 56 elements that have two or more isotopes, however, remains relatively little explored, but is gaining rapid attention, in part driven by advances in analytical instrumentation in the last 5-10 years. Our goal for this volume was to bring together a summary of the isotope geochemistry of non-traditional stable isotope systems as is known through 2003 for those elements that have been studied in some detail, and which have a variety of geochemical properties. In addition, recognizing that many of these elements are of interest to workers who are outside the traditional stable isotope fields, we felt it was important to include discussions on the broad isotopic variations that occur in the solar system, theoretical approaches to calculating isotopic fractionations, and the variety of analytical methods that are in use. We hope, therefore, that this volume proves to be useful to not only the isotope specialist, but to others who are interested in the contributions that these non-traditional stable isotopes may make toward understanding geochemical and biological cycles.

Description / Table of Contents: Part I: Introduction. - Part II: Environmental Chemist's Toolbox. - Part III: The Atmosphere. - Part IV: The Chemistry Of Continental Solids. - Part V: The Chemistry Of Continental Waters. - Part VI: The Oceans. - Part VII: Global Change

Description / Table of Contents: Contents: Preface. - List of contributors. - 1. Mathematical models for the interpretation of environmental radioisotopes in groundwater systems. - 2. Isotopes in cloud physics: multiphase and multistage condensation processes. - 3. Environmental isotopes in lake studies. - 4. Environmental isotope and anthropogenic tracers of recent lake sedimentation. - 5. Stable isotope geochemistry of travertines. - 6. Isotope geochemistry of carbonates in the weathering zone. - 7. Geochronology and isotopic geochemistry of speleothems. - 8. Oxygen and hydrogen isotope geochemistry of deep basin brines. - 9. Isotope effects of nitrogen in the soil and biosphere. - 10. Chlorine-36 in the terrestrial environment. - 11. Radioactive noble gases in the terrestrial environment. - 12. Isotopes and food.

Description / Table of Contents: This volume summarizes the main results of a priority programme of the Deutsche Forschungsgemeinschaft (DFG), Bonn-Bad Godesberg

Description / Table of Contents: The book summarizes the knowledge and experiences concerning the role of halogens during various geochemical processes, such as diagenesis, ore-formation, magma evolution, metasomatism, mineralization, and metamorphism in the crust and mantle of the Earth. It comprises the role of halogens in other terrestrial worlds like volatile-rich asteroids, Mars, and the ice moons of Jupiter and Saturn. Review chapters outline and expand upon the basis of our current understanding regarding how halogens contribute to the geochemical/geophysical evolution and stability of terrestrial worlds overall.

Description / Table of Contents: The IUGS/IAGC Global Geochemical Baselines Programme aims to establish a global geochemical reference baseline for 〉60 determinants in a range of media for environmental and other applications. The European contribution to the programme has been carried out by government institutions from 26 countries under the auspices of the Forum of European Geological Surveys (FOREGS) The main objectives of this European survey were: 1) to apply standardised methods of sampling, chemical analysis and data management to prepare a geochemical baseline across Europe; and 2) to use this reference network to level national baseline datasets. Samples of stream water, stream sediment and three types of soil (organic top layer, minerogenic top and sub soil) have been collected at 900 stations, each representing a catchment area of 100 km2, corresponding to a sampling density of about one sample per 4700 km2. In addition, the uppermost 25 cm of floodplain sediment was sampled from 790 sites each representing a catchment area of 1000 km2. All soil and sediment samples were prepared at the same laboratory, and all samples of particular sample types were analysed by the same method at the same laboratory. More than 50 elements, both total and aqua regia extractable concentrations, and other parameters (such as pH and grain size) were determined on the 〈2 mm grain size fraction of minerogenic samples, and total concentrations of organic soil samples were measured after using a strong acid digestion. Nine laboratories of European geological surveys carried out the analytical work. Altogether, 360 geochemical maps showing the distribution of elements across Europe have been prepared. All the results and field observations are organised in a common database and the maps are published as a Geochemical Atlas of Europe. All the sampling sites were photographed and this photo archive is also available. Samples have been archived in the Slovak Republic for possible future use. Initial results show that the distribution patterns of both water and solid samples are related to such factors as large-scale tectonic provinces, geochemical variation of large lithological units, extension of the Weichselian glaciation, and contamination reflecting industrialized areas and regions of intensive agriculture. Key words (GeoRef Thesaurus, AGI): geochemical surveys, baseline studies, soils, sediments, stream water, sampling, sample preparation, chemical analysis, geochemical maps, atlas, areal geology, Europe

Description / Table of Contents: Contents: 1. Isotopes and radioactivity; 2. The principles o radioactive dating; 3. Radiometric dating methods; 4. Dating by cosmogenic isotopes; 5. Uncertainties and results of radiometric dating; 6. Radiogenic isotope geochemistry; 7. Stable isotope geochemistry; 8. Isotope geology and dynamic reservoir analysis

Description / Table of Contents: Microorganisms cause mineral precipitation and dissolution and control the distribution of elements in diverse environments at and below the surface of the Earth. Conversely, mineralogical and geochemical factors exert important controls on microbial evolution and the structure of microbial communities. This was the rationale for the Short Course on Geomicrobiology presented by the Mineralogical Society of America on October 18 and 19, 1997, at the Alta Peruvian Lodge in Alta, Utah. Minerals have been known and honored since humans realized their essential contributions to the "terra firma" and stone tools thrust our species on the path of cultural evolution. Microbes are the oldest living creatures, probably inhabiting at least a few salubrious environments on the earth as early as 3.8 billion years ago. At this moment in history we are only beginning to appreciate the intimate juxtaposition and interdependence of minerals and microbes. We have been nudged into this position by the realization that our earth is finite, and the recognition of many global environmental problems that minerals and microbes contribute to, both positively and negatively. In addition, our globe may not be the only site in the solar system where 'life' arose, or may persist. What all of these concerns enunciate is that we as scientists only dimly comprehend our own dynamic "terrestrial halls." This short course and volume have been generated with great enthusiasm for grasping as much as possible of the whole panorama of possibilities that involve both the inorganic and biologic realms . Over 3600 mineral species have been defined and their relationships to each other and the environments in which they form have been documented. This vast data base, collected over the past several hundred years and constantly added to and upgraded, is a monument to the research efforts of many geoscientists focused on the inorganic realm. Much of this data has come from investigators intrigued by the novelty, beauty, and versatility of minerals, direct expressions of the chemistry and physics of geologic processes. We are now adding a new dimension to questions of mineral formation, dissolution, and distribution: what were, are, and will be the contributions of microbes to these basic components of the environment. Microbes have also been known for hundreds of years. However, their small size (0.5 to 5 µm in diameter) and the difficulties associated with identifying a species unless it was grown in the laboratory (cultured), precluded thorough analysis. The advent of molecular biology has only recently made it possible to evaluate microbial evolutionary relatedness (phylogeny) and physiological diversity. These techniques are now being applied to study of microbial populations in natural environments. It is becoming very clear that the surface of Earth is populated by far more species of microbes than there are types of minerals. We are now exploring every portion of the globe and finding the relationships under the rubric "geomicrobiology." The ocean deeps are characterized by a diversity of microorganisms, including those associated with manganese nodules. The profusion and concentration of minerals created at ocean ridges and vents matches the variety of microorganisms, large animals, and plants there. The snowy tops of mountain ranges and glaciers of Antarctica harbor not just ice but whole bacterial communities whose cellular types and activities need elucidation. The equatorial jungles and the deserts, with their enormous diversity of ecological niches, further challenge us. The diversity of geographic, geologic, and biologic environments, including some contributed by humans (e.g. mines, air-conditioning equipment), can now also be explored in detail. Modern studies use protocols developed to preserve or measure in situ chemical and physical characteristics. Electron microscopes allow direct characterization of mineral and biological morphology and internal structures. Spectroscopic techniques permit complimentary chemical analysis, including determination of oxidation states, with very high spatial resolution. Other studies quantitatively measure isotopic abudances. These data serve to distinguish biologically mediated, or biologically controlled formation of the mineral from an abiotic process and mechanism. Each ecological niche requires accurate characterization of the mineralogic and biologic entities in order for us to begin to understand the range of dynamic relationships. We can pose many questions. Is the mineral only a substrate, or is its occurrence and stability impacted by microbiologic activity and metabolic requirements? Which minerals are of microbiological rather than inorganic origin and what are the mechanisms by which organisms dictate the morphology and structure of the solid phase formed? How do organic metabolic products bind metals and change their form and distribution, with implications for metal toxicity and geochemical cycles? How do inorganic reactions such as mineral dissolution and precipitation impact microbial populations through control of their physical and chemical environments? Clearly, new and excitingly research areas exist for all varieties of scientists. Although published by the Mineralogical Society of America, the authors of this volume include microbiologists, molecular biologists, biochemists, biophysicists, bioengineers as well as biomineralogists. Here, they bring together their respective expertise and perspectives to provide disciplinary and interdisciplinary background needed to define and further explore the topic of geomicrobiology. The volume is organized so as to first introduce the nature, diversity, and metabolic impact of microorganisms and the types of solid phases they interact with. This is followed by a discussion of processes that occur at cell surfaces, interfaces between microbes and minerals, and within cells, and the resulting mineral precipitation, dissolution, and changes in aqueous geochemistry. The volume concludes with a discussion of the carbon cycle over geologic time. In detail: Nealson and Stahl acquaint us with the basic properties of prokaryotes, including their size and structure. They define the types and ranges of microorganisms and their metabolisms and describe their impacts on some important biogeochemical cycles. Barns and Nierzwicki-Bauer document the phylogenetic relationships and evolution of microorganisms, begging some fundamental questions that might be now just beyond our grasp: What was the 'last common ancestor'? The physiology, biochemistry and ecology of hyperthermophilic, and the many diverse geologically important microbial species from the lithosphere and hydrosphere, as well as some of the techniques employed, are presented. Banfield and Hamers describe and integrate the processes acting on minerals and at surfaces relevant to microorganisms, examining the factors that control mineralogy, mineral forms, and the stability of phases. Surface properties and reaction rates for dissolution, precipitation, and growth of important classes of minerals are discussed. The possible role of mineral surfaces in formation of prebiotic molecules needed to explain the origin of life is examined. Little, Wagner and Lewandowski describe biofilms, an essential interface between microbes and minerals. They demonstrate that these membranes, with their unique morphological and structural attributes, are sites where much activity related to dissolution and/or formation of minerals takes place. Biology makes it possible to move molecules and elements against a gradient. Many questions regarding the transfer of elements from minerals to microbes at this important heterogeneous interface remain. Fortin, Ferris and Beveridge review surface-mediated mineral development by bacteria. Fresh or oceanic waters, anaerobic or aerobic environments provide discretely different ecologies, bacterial entities, and resulting mineralogies. It is obvious from this presentation that investigators have just scratched the surface of microbial mineralization processes. Bazlinski and Moskowitz review the magnetic biominerals and provide insights into the environmental and biological significance of these few tens of nanometer-sized mineral products. The magnetosome chemistry and biochemistry is probably the best understood of any biologically precipitated mineral. Their formation and unique properties underscore the roles these biomaterials play in the rock magnetic record and in geochemical cycles. Tebo, Ghiorse, van Waasbergen, Siering and Caspi contribute data on the roles of Mnminerals and Mn(II) oxidation in geologic environments. Their chapter encompasses molecular genetic and biochemical investigations. Manganese oxides and oxyhydroxides are notoriously difficult to identify and the crystal chemistry of these phases is a research effort on its own. The prospect of learning how microbes utilize the multiple oxidation states of Mn (2+, 3+ and 4+) as a source of energy sharpens the motivation for interdisciplinary study. Manganese is also known as a cofactor in the production and activation of the enzymes that digest large biomolecules that must be the source of the smaller molecular species and ultimately the building blocks of C, N, 0, H required by all species. How have the mechanisms identified in the bacterial systems been transferred up the phylogenetic tree to plants and humans? This is an expanding and intriguing area for further investigation. DeVrind-de Jong and de Vrind address silicate and carbonate deposition by algae (eukaryotic photosynthetic microorganisms). This chapter documents the mechanisms of biomineralization of diatoms and coccoliths. These abundant aquatic organisms are responsible for huge volumes of siliceous sediments and calcium carbonate deposits world wide. The implications of algal biomineralization for climatic variation throughout much of the Earth's history may be quite significant. Stone leads us though a quantitative approach to evaluating reactions between organic molecules and cations. He considers available extracellular organic ligands and the roles these play in uptake of metals. He documents the basic chemical speciation and complexation for several elements, making metal to metal comparisons. Remaining challenges involve coordinating the organic and inorganic results of biologic activity. Following the discussion of biomineralization and interactions between organic compounds and cations, Silver discusses the strategies microorganisms have evolved to deal with toxic metal concentrations in solution. Beyond the fundamental biological significance, this has important implications for understanding microbial populations in contaminated environments. The impact on the geochemical form (speciation) and distribution of elements is also discussed. Nordstrom and Southam summarize sulfide mineral oxidation and dissolution kinetics and devote considerable effort to describing the specific contributions of microorganisms, mostly bacteria. Despite the vast amount of accumulated information, many unanswered questions remain. Barker, Welch and Banfield address weathering of silicate minerals. This topic encompasses not only mineralogy but geomorphology, microbiology, and geochemistry. The necessary interdisciplinary mode of these investigations is highlighted by discussion of the role(s) of bacterial nutrition, groundwater chemistry, and biochemistry. There are obvious implications for hazardous waste storage, a currently daunting and politicized topic that requires predictions over thousands to millions of years. Finally, Des Marais treats the long term evolution of the carbon cycle, adopting a biogeochemical view. He discusses the sources, sinks and the transfer of the element over geologic time. Consideration of such a basic series of questions relating to the partitioning of carbon necessitate interdisciplinary crossovers. It is a fitting conclusion to a dialogue in progress.

Description / Table of Contents: Content: Partial table of contents: Hydrothermal Mineral Deposits: What We Do and Don Know (B. Skinner). Magmas and Hydrothermal Fluids (C. Burnham). Thermal Aspects of Ore Formation (L. Cathles). Oxygen and Hydrogen Isotope Relationships in Hydrothermal Mineral Deposits (H. Taylor). Hydrothermal Alteration and Its Relationship to Ore Fluid Composition (M. Reed). Sulfide Ore Mineral Stabilities, Morphologies, and Intergrowth Textures (D. Vaughan & J. Craig). Gangue Mineral Transport and Deposition (J. Rimstidt). Fluid Inclusion Studies of Hydrothermal Ore Deposits (E. Roedder & R. Bodnar). Geothermal Systems and Mercury Deposits (H. Barnes & T. Seward). Submarine Hydrothermal Systems and Deposits (S. Scott). Ore-Forming Brines in Active Continental Rifts (M. McKibben & L. Hardie). Appendix. Index.

Description / Table of Contents: Over 25 years ago, Volume 9 of Reviews in Mineralogy: Amphiboles and Other Hydrous Pyriboles seemed to contain all that was possible to know about this group of fascinating minerals. The subsequent twenty-five years have shown that this assessment was wrong: Nature was keeping a lot in reserve, and has since revealed considerable new complexity in the constitution and behavior of amphiboles. Some of the advances in knowledge have been due to the use of new experimental techniques, some have been due to the investigation of hitherto neglected rock-types, and some have been due to the development of new ideas. The identification and systematic investigation of variable LLE (Light Lithophile Elements), particularly Li and H, led to the identification of several new amphibole species and the recognition that variable Li and H play an important role in chemical variations in amphiboles from both igneous and metamorphic parageneses. In turn, this work drove the development of microbeam SIMS to analyze LLE in amphiboles. Detailed mineralogical work on metasyenites showed hitherto unexpected solid-solution between Na and Li at the M(4) site in monoclinic amphiboles, a discovery that has upset the current scheme of amphibole classification and nomenclature and initiated new efforts in this direction. Systematic and well-planned synthesis of amphiboles, combined with careful spectroscopy, has greatly furthered our understanding of cation and anion order in amphiboles. The use of bond-valence theory to predict patterns of SRO (Short-Range Order) in amphiboles, and use of these predictions to understand the infrared spectra of well-characterized synthetic-amphibole solid-solutions, has shown that SRO is a major feature of the amphibole structure, and has resulted in major advances in our understanding of SRO in minerals. There has been significant progress relating changes in amphibole composition and cation ordering to petrogenetic conditions and trace-element behavior. Work on the nature of fibrous amphiboles and their toxicity and persistence in living organisms has emphasized the importance of accurate mineralogical characterization in environmental and health-related problems. The current volume has taken a different approach from previous volumes concerned with major groups of rock-forming minerals. Some of the contents have previously been organized by the investigative technique or groups of similar techniques: crystal-structure refinement, spectroscopy, TEM etc. Here, we have taken an approach that focuses on aspects of amphiboles rather than experimental techniques: crystal chemistry, new compositions, long-range order, short-range order etc., and all experimental results germane to these topics are discussed in each chapter. The intent of this approach is to focus on amphiboles, and to emphasize that many techniques are necessary to fully understand each aspect of the amphiboles and their behavior in both natural and industrial processes.

Description / Table of Contents: Contents: 1. The Discovery of Silicate Melts. An Industrial and Geological Perspective. 2. Glass Versus Melt. 3. Glasses and Melts vs. Crystals. 4. Melt and Glass Structure - Basic Concepts. 5. Silica - A Deceitful Simplicity. 6. Binary Metal Oxide-Silica Systems I. Physical Properties.7. Binary Metal Oxide-Silica Systems II. Structure. 8. Aluminosilicate Systems I. Physical Properties. 9. Aluminosilicate Systems II. Structure. 10. Iron-bearing Melts I. Physical Properties. 11. Iron-bearing Melts II. Structure. 12. The Titanium Anomalies. 13. Phosphorus. 14. Water - An Elusive Component. 15. Volatiles I. The System C-O-H-S. 16. Volatiles II. Noble Gases and Halogens. 17. Natural Melts.

Description / Table of Contents: The 32 research papers in this volume examine the mode and nature of igneous, metamorphic, tectonic, sedimentological and biological processes associated with the evolution of ophiolites in Earth's history. Divided into six sections, the book presents a wealth of new data and syntheses from ophiolites around the world. Introductory chapters review the distribution of ophiolites in space and time and present a synoptic discussion on their importance in Earth history. Papers in the second section present diverse data from Tethyan ophiolites and provide refined geodynamic models for their evolution. The following two sections present case studies documenting magmatic, metamorphic and tectonic processes in ophiolite genesis and hydrothermal and biogenic alteration of fossil oceanic crust. Mechanisms of ophiolite emplacement are explored in Section V with a focus on the Semail massif (Oman). The last section examines the regional occurrence and geodynamic significance of ophiolite belts on different continents. The book reflects the contemporary work of the international community in a most up-to-date treatment of process-oriented questions on the evolution of ophiolites.

Description / Table of Contents: The idea for this book was conceived in early June, 2005 at a paleoaltimetry workshop held at Lehigh University, Lehigh, Pennsyalvania and organized by Dork Sahagian. The workshop was funded by the tectonics program at NSF, and was designed to bring together researchers in paleoaltimetry to discuss different techniques and focus the community on ways of improving paleoelevation estimates and consequent interpretations of geodynamics and tectonics. At this meeting, some commented that a comprehensive volume describing the different methods could help advance the field. I offered to contact the Mineralogical Society of America and the Geochemical Society about publishing a RiMG volume on paleoaltimetry. Because many of the techniques used to infer paleoelevations are geochemically-based or deal with thermodynamic principles, the GS and MSA agreed to the project. Two years and roughly 1000 e-mails later, our book has arrived. The book is organized into 4 sections: Geodynamic and geomorphologic rationale (Clark). This chapter provides the broad rationale behind paleoaltimetry, i.e., why we study it. Stable isotope proxies. These 4 chapters cover theory of stable isotopes in precipitation and their response to altitudinal gradients (Rowley), and stable isotopes sytematics in paleosols (Quade, Garzione and Eiler), silicates (Mulch and Chamberlain) and fossils (Kohn and Dettman). Proxies of atmospheric properties. These 4 chapters cover temperature lapse rates (Meyer), entropy (Forest), and atmospheric pressure proxies, including total atmospheric pressure from gas bubbles in basalt (Sahagian and Proussevitch), and the partial pressure of CO2 (Kouwenberg, Kürshner, and McElwain). Note that clumped isotope thermometry (Quade, Garzione and Eiler) also provides direct estimates of temperature. Radiogenic and cosmogenic nuclides. These 2 chapters cover low-temperature thermochronologic approaches (Reiners) and cosmogenic isotopes (Riihimaki and Libarkin). Some chapters overlap in general content (e.g., basic principles of stable isotopes in precipitation are covered to different degrees in all stable isotope chapters), but no attempt was made to limit authors' discussion of principles, or somehow attempt to arrive at a "consensus view" on any specific topic. Because science advances by critical discussion of concepts, such restrictions were viewed as counterproductive. This does mean that different chapters may present different views on reliability of paleoelevation estimates, and readers are advised to read other chapters in the book on related topics – they may be more closely linked than they might at first appear! I hope readers of this book will discover and appreciate the synergy among paleoaltimetry, climate change, and tectonic geomorphology. These interrelationships create a complex, yet rich field of scientific enquiry that in turn offers insights into climate and geodynamics.

Description / Table of Contents: Hydrogen may be the most abundant element in the universe, but in science and in nature oxygen has an importance that is disproportionate to its abundance. Human beings tend to take it for granted because it is all around us and we breathe it, but consider the fact that oxygen is so reactive that in a planetary setting it is largely unstable in its elemental state. Were it not for the constant activity of photosynthetic plants and a minor amount of photo dissociation in the upper atmosphere, we would not have an oxygen-bearing atmosphere and we would not be here. Equally, the most important compound of oxygen is water, without which life (in the sense that we know it) could not exist. The role of water in virtually all geologic processes is profound, from formation of ore deposits to igneous petrogenesis to metamorphism to erosion and sedimentation. In planetary science, oxygen has a dual importance. First and foremost is its critical role in so many fundamental Solar System processes. The very nature of the terrestrial planets in our own Solar System would be much different had the oxygen to carbon ratio in the early solar nebula been somewhat lower than it was, because elements such as calcium and iron and titanium would have been locked up during condensation as carbides, sulfides and nitrides and even (in the case of silicon) partly as metals rather than silicates and oxides. Equally, the role of water ice in the evolution of our Solar System is important in the early accretion and growth of the giant planets and especially Jupiter, which exerted a major control over how most of the other planets formed. On a smaller scale, oxygen plays a critical role in the diverse kinds of physical evolution of large rocky planets, because the internal oxidation state strongly influences the formation and evolution of the core, mantle and crust of differentiated planets such as the Earth. Consider that basaltic volcanism may be a nearly universal phenomenon among the evolved terrestrial planets, yet there are basalts and basalts. The basalts of Earth (mostly), Earth's Moon, Vesta (as represented by the HED meteorites) and Mars are all broadly tholeiitic and yet very different from one another, and one of the primary differences is in their relative oxidation states (for that matter, consider the differences between tholeiitic and calc-alkaline magma series on Earth). But there is another way that oxygen has proven to be hugely important in planetary science, and that is as a critical scientific clue to processes and conditions and even sources of materials. Understanding the formation and evolution of our Solar System involves reconstructing processes and events that occurred more than 4.5 Ga ago, and for which the only contemporary examples are occurring hundreds of light years away. It is a detective story in which most of the clues come from the laboratory analysis of the products of those ancient processes and events, especially those that have been preserved nearly unchanged since their formation at the Solar System's birth: meteorites; comets; and interplanetary dust particles. For example, the oxidation state of diverse early Solar System materials ranges from highly oxidized (ferric iron) to so reducing that some silicon exists in the metallic state and refractory lithophile elements such as calcium exist occur in sulfides rather than in silicates or carbonates. These variations reflect highly different environments that existed in different places and at different times. Even more crucial has been the use of oxygen 3-isotope variations, which began almost accidentally in 1973 with an attempt to do oxygen isotope thermometry on high-temperature solar nebula grains (Ca-, Al-rich inclusions) but ended with the remarkable discovery of non-mass-dependent oxygen isotope variations in high-temperature materials from the earliest Solar System. The presolar nebula was found to be very heterogeneous in its isotopic composition, and virtually every different planet and asteroid for which we have samples has a unique oxygen-isotopic fingerprint. The idea for this book originated with Jim Papike, who suggested the idea of a study initiative (and, ultimately, a published volume) focused on the element that is so critically important in so many ways to planetary science. He recognized that oxygen is such a constant theme through all aspects of planetary science that the proposed initiative would serve to bring together scientists from a wide range of disciplines for the kind of cross-cutting dialogue that occurs all too rarely these days. In this sense the Oxygen Initiative is modeled on the Basaltic Volcanism Study Project, which culminated in what remains to this day a hugely important reference volume (Basaltic Volcanism Study Project 1981). After obtaining community input and feedback, primarily through the Curation and Analysis Planning Team for Extraterrestrial Materials (CAPTEM) and the Management Operations Working Group for NASA's Cosmochemistry Program, a team of scientists was assembled who would serve as chapter writing leads, and the initiative was formally proposed to and accepted by the Lunar and Planetary Institute (LPI; Dr. Stephen Mackwell, Director) for sponsorship. A formal proposal was then submitted to and approved by the Mineralogical Society of America to publish the resulting volume in the Reviews in Mineralogy and Geochemistry (RiMG) series. Three open workshops were held as preludes to the book: Oxygen in the Terrestrial Planets, held in Santa Fe, NM July 20-23, 2004; Oxygen in Asteroids and Meteorites, held in Flagstaff, AZ June 2-3, 2005; and Oxygen in Earliest Solar System Materials and Processes (and including the outer planets and comets), held in Gatlinburg, TN September 19-22, 2005. The workshops were each organized around a small number of sessions (typically 4-6), each focusing on a particular topic and consisting of invited talks, shorter contributed talks, and ample time for discussion after each talk. In all of the meetings, the extended discussion periods were lively and animated, often bubbling over into the breaks and later social events. As a consequence of the cross-cutting approach, the final book spans a wide range of fields relating to oxygen, from the stellar nucleosynthesis of oxygen, to its occurrence in the interstellar medium, to the oxidation and isotopic record preserved in 4.56 Ga grains formed at the Solar System's birth, to its abundance and speciation in planets large and small, to its role in the petrologic and physical evolution of the terrestrial planets.

Description / Table of Contents: The authors of this volume presented a short course on the rare earth elements to about 80 participants in San Francisco, California, December 1-3, 1989, just prior to the fall meeting of the American Geophysical Union.

Description / Table of Contents: In situ-produced cosmogenic nuclides can provide chronologies of environmental change over the past few thousand to several millions of years and may be used to quantify a wide range of weathering and sediment transport processes. These nuclides are thus now used across a broad spectrum of earth science disciplines, including paleoclimatology, geomorphology, and active tectonics. This book is organized around sections that focus on specific aspects of the utilization of cosmogenic nuclides in earth sciences: (1) development of new methods for application of in situ-produced cosmogenic nuclides (burial dating methods, extending their utilization to carbonate-rich and mafic environments); (2) glacial geology (Laurentide Ice Sheet, northern Alps); (3) active tectonics, focusing on applications to constrain slip rates of active faults in Asia (Tibet and Mongolian Gobi-Altay); and (4) landscape development (quantifying sediment production or erosion rates and processes and application of exposure dating to landslides in Hong Kong).