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Nitrogen is an essential nutrient for life, and its sources and cycling have varied over earth history. Stable isotope ratios of nitrogen compounds (expressed as δ15N, in ‰) are preserved in the sedimentary record and track these changes, providing important insights into associated biogeochemical feedbacks. Here we review the use of nitrogen stable isotope geochemistry in unravelling the evolution of the global N cycle in deep time. We highlight difficulties with preservation, unambiguous interpretations, and local versus global effects. We end with several case studies illustrating how depositional and stratigraphic context is crucial in reliably interpreting δ15N records in ancient marine sediments, both in ancient anoxic (Archean) and more recent well oxygenated (Phanerozoic) environments.
A comprehensive progress report on the multi-disciplinary field of ocean and climate change research is given. It compiles introductory background papers and leading scientific results on the ocean-atmosphere carbon cycle with emphasis on the ocean's carbon inventory and the various components involved. The relationship between plankton productivity, carbon fixation, oceanic PCO2 and climate change is investigated from the viewpoint of long-term climatic change during the late Quaternary cycles of ice ages and warm ages. The various approaches range from micropaleontology over organic and trace element geochemistry to molecular isotope geochemistry.
Nitrogen in the Marine Environment provides information pertinent to the many aspects of the nitrogen cycle. This book presents the advances in ocean productivity research, with emphasis on the role of microbes in nitrogen transformations with excursions to higher trophic levels. Organized into 24 chapters, this book begins with an overview of the abundance and distribution of the various forms of nitrogen in a number of estuaries. This text then provides a comparison of the nitrogen cycling of various ecosystems within the marine environment. Other chapters consider chemical distributions and methodology as an aid to those entering the field. This book discusses as well the enzymology of the initial steps of inorganic nitrogen assimilation. The final chapter deals with the philosophy and application of modeling as an investigative method in basic research on nitrogen dynamics in coastal and open-ocean marine environments. This book is a valuable resource for plant biochemists, microbiologists, aquatic ecologists, and bacteriologists.
In the modern marine environment, barium isotope (δ138Ba) variations are primarily driven by barite cycling—barite incorporates 'light' Ba isotopes from solution, rendering the residual Ba reservoir enriched in 'heavy' Ba isotopes by a complementary amount. Since the processes of barite precipitation and dissolution are vertically segregated and spatially heterogeneous, barite cycling drives systematic variations in the barium isotope composition of seawater and sediments. This Element examines these variations; evaluates their global, regional, local, and geological controls; and, explores how δ138Ba can be exploited to constrain the origin of enigmatic sedimentary sulfates and to study marine biogeochemistry over Earth's history.
Magnesium is a major constituent in silicate and carbonate minerals, the hydrosphere and the biosphere. Magnesium is constantly cycled between these reservoirs. Since each of the major planetary reservoirs of magnesium have different magnesium isotope ratios, there is scope to use magnesium isotope ratios to trace 1) the processes that cycle Magnesium at a spatial scales from the entire planet to microscopic and 2) the relative fluxes between these reservoirs. This review summarises some of the key motivations, successes and challenges facing the use of magnesium isotopes to construct a budget of seawater magnesium, present and past.
Studies of Sr isotopic composition of thousands of samples of marine sediments and fossils have yielded a curve of 87Sr/86Sr versus age for seawater Sr that extends back to 1 billion years. The ratio has fluctuated with large amplitude during this time period, and because the ratio is always uniform in the oceans globally at any one time, it is useful as a stratigraphic correlation and age-dating tool. The ratio also appears to reflect major tectonic and climatic events in Earth history and hence provides clues as to the causes, timing, and consequences of those events. The seawater 87Sr/86Sr ratio is generally high during periods marked by continent-continent collisions, and lower when continental topography is subdued, and seafloor generation rates are high. There is evidence that major shifts in the seawater ratio can be ascribed to specific orogenic events and correlate with large shifts in global climate.
Over million-year timescales, the geologic cycling of carbon controls long-term climate and the oxidation of Earth's surface. Inferences about the carbon cycle can be made from time series of carbon isotopic ratios measured from sedimentary rocks. The foundational assumption for carbon isotope chemostratigraphy is that carbon isotope values reflect dissolved inorganic carbon in a well-mixed ocean in equilibrium with the atmosphere. However, when applied to shallow-water platform environments, where most ancient carbonates preserved in the geological record formed, recent research has documented the importance of considering both local variability in surface water chemistry and diagenesis. These findings demonstrate that carbon isotope chemostratigraphy of platform carbonate rarely represent the average carbonate sink or directly records changes in the composition of global seawater. Understanding what causes local variability in shallow-water settings, and what this variability might reveal about global boundary conditions, are vital questions for the next generation of carbon isotope chemostratigraphers.
Geologic Time Scale 2020 (2 volume set) contains contributions from 80+ leading scientists who present syntheses in an easy-to-understand format that includes numerous color charts, maps and photographs. In addition to detailed overviews of chronostratigraphy, evolution, geochemistry, sequence stratigraphy and planetary geology, the GTS2020 volumes have separate chapters on each geologic period with compilations of the history of divisions, the current GSSPs (global boundary stratotypes), detailed bio-geochem-sequence correlation charts, and derivation of the age models. The authors are on the forefront of chronostratigraphic research and initiatives surrounding the creation of an international geologic time scale. The included charts display the most up-to-date, international standard as ratified by the International Commission on Stratigraphy and the International Union of Geological Sciences. As the framework for deciphering the history of our planet Earth, this book is essential for practicing Earth Scientists and academics. - Completely updated geologic time scale - Provides the most detailed integrated geologic time scale available that compiles and synthesize information in one reference - Gives insights on the construction, strengths and limitations of the geological time scale that greatly enhances its function and its utility
Molybdenum (Mo) is a widely used trace metal for investigating redox conditions. However, unanswered questions remain that concentration and bulk isotopic analysis cannot specially answer. Improvements can be made by combining new geochemical techniques to traditional methods of Mo analysis. In this Element, we propose a refinement of Mo geochemistry within aquatic systems, ancient rocks, and modern sediments through molecular geochemistry (systematically combining concentration, isotope ratio, elemental mapping, and speciation analyses). Specifically, to intermediate sulfide concentrations governing Mo behavior below the 'switch-point' and dominant sequestration pathways in low oxygen conditions. The aim of this work is to 1) aid and improve the breadth of Mo paleoproxy interpretations by considering Mo speciation and 2) address outstanding research gaps concerning Mo systematics (cycling, partitioning, sequestration, etc.). The Mo paleoproxy has potential to solve ever complex research questions. By using molecular geochemical recommendations, improved Mo paleoproxy interpretations and reconstruction can be achieved.