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  • 1
    Monograph available for loan
    Monograph available for loan
    Washington, D.C. : Mineralogical Society of America
    Associated volumes
    Call number: 11/M 04.0253
    In: Reviews in mineralogy & geochemistry
    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.
    Type of Medium: Monograph available for loan
    Pages: XV, 454 S. , Ill., graph. Darst
    ISBN: 0-939950-67-7 , 978-0-939950-67-6
    ISSN: 1529-6466
    Series Statement: Reviews in mineralogy & geochemistry 55
    Classification:
    Geochemistry
    Note: Chapter 1. Overview and General Concepts by Clark M. Johnson, Brian L. Beard and Francis Albarede, p. 1 - 24 Chapter 2. An Overview of Isotopic Anomalies in Extraterrestrial Materials and Their Nucleosynthetic Heritage by Jean Louis Birck, p. 25 - 64 Chapter 3. Applying Stable Isotope Fractionation Theory to New Systems by Edwin A. Schauble, p. 65 - 112 Chapter 4. Analytical Methods for Non-Traditional Isotopes by Francis AlbarÀde and Brian L. Beard, p. 113 - 152 Chapter 5. Developments in the Understanding and Application of Lithium Isotopes in the Earth and Planetary Sciences by Paul B. Tomascak, p. 153 - 196 Chapter 6. The Isotope Geochemistry and Cosmochemistry of Magnesium by Edward D. Young and Albert Galy, p. 197 - 230 Chapter 7. The Stable-Chlorine Isotope Compositions of Natural and Anthropogenic Materials by Michael A. Stewart and Arthur J. Spivack, p. 231 - 254 Chapter 8. Calcium Isotopic Variations Produced by Biological, Kinetic, Radiogenic and Nucleosynthetic Processes by Donald J. DePaolo, p. 255 - 288 Chapter 9. Mass-Dependent Fractionation of Selenium and Chromium Isotopes in Low-Temperature Environments by by Thomas M. Johnson and Thomas D. Bullen, p. 289 - 318 Chapter 10A. Fe Isotope Variations in the Modern and Ancient Earth and Other Planetary Bodies by Brian L. Beard and Clark M. Johnson, p. 319 - 358 Chapter 10B. Isotopic Constraints on Biogeochemical Cycling of Fe by Clark M. Johnson, Brian L. Beard, Eric E. Roden, Dianne K. Newman and Kenneth H. Nealson, p. 359 - 408 Chapter 11. The stable isotope geochemistry of copper and zinc by Francis Albarede, p. 409 - 428 Chapter 12. Molybdenum Stable Isotopes: Observations, Interpretations and Directions by Ariel D. Anbar, p. 429 - 454
    Location: Reading room
    Branch Library: GFZ Library
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  • 2
    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.
    Pages: Online-Ressource (XVI, 454 Seiten)
    ISBN: 0939950677
    Language: English
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  • 3
    Publication Date: 2023-08-28
    Keywords: Alpha Ridge, Arctic Ocean; CAMECA SX50 electron microprobe; Cerium; CESAR; CESAR_83-011; DEPTH, sediment/rock; Dysprosium; Erbium; Europium; Event label; FL-275; FL-286; FL-380; FL-443; Gadolinium; GC; Gravity corer; Identification; Iron; Manganese; Mass spectrometer VG Sector 54; Neodymium; Rubidium; Rubidium-87/Strontium-86 ratio; Samarium; Sampling/drilling from ice; Sampling/drilling ice; Strontium; Strontium-87/Strontium-86 ratio; Strontium-87/Strontium-86 ratio, error; T-3; Ytterbium
    Type: Dataset
    Format: text/tab-separated-values, 222 data points
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  • 4
    Publication Date: 2023-08-28
    Keywords: Alpha Ridge, Arctic Ocean; Aluminium oxide; Aluminium oxide, standard deviation; Calcium oxide; Calcium oxide, standard deviation; CESAR; CESAR_83-011; Cobalt; Cobalt, standard deviation; Copper; Copper, standard deviation; DEPTH, sediment/rock; Description; Electron microprobe (EMP); Event label; FL-286; GC; Geologic age name; Gravity corer; Identification; Iron; Iron, standard deviation; Magnesium oxide; Magnesium oxide, standard deviation; Manganese; Manganese, standard deviation; Nickel; Nickel, standard deviation; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Number; Potassium oxide; Potassium oxide, standard deviation; Sampling/drilling from ice; Sampling/drilling ice; Silicon dioxide; Silicon dioxide, standard deviation; T-3; Zinc; Zinc, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 1003 data points
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  • 5
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    Unknown
    PANGAEA
    In:  Supplement to: Winter, Bryce L; Johnson, Clark M; Clark, David L (1997): Geochemical constraints on the formation of Late Cenozoic ferromanganese micronodules from the central Arctic Ocean. Marine Geology, 138(1-2), 149-169, https://doi.org/10.1016/S0025-3227(97)00013-3
    Publication Date: 2023-08-28
    Description: In order to determine geochemical compositions of Late Cenozoic Arctic seawater, oxide fractions were chemically separated from 15 samples of hand-picked ferromanganese micronodules (50-300 mu m). The success of the chemical separation is indicated by the fact that 〉97% of the Sr in the oxide fraction is seawater-derived. Rare-earth element (REE) abundances of the Arctic micronodule oxide fractions are much lower than those of bulk Fe-Mn nodules from other ocean basins of the world (e.g., 33 vs. 145 ppm Nd), but the Arctic oxides are enriched in Ce relative to Nd (Ce-N/Nd-N=2.2+/-0.5) and have convex-upward, shale-normalized REE patterns (Nd-N/Gd-N=0.61+/-0.06, Gd-N/Yb-N = 1.5+/-0.2, Nd-N/Yb-N = 0.9+/-0.2), typical of other hydrogenous and diagenetic marine Fe-Mn-oxides. Bulk sediment samples from the central Arctic Ocean have REE abundances and patterns that are characteristic of those of post-Archean shale. Non-detrital fractions (calcite + oxide coatings) of Recent Arctic foraminifera have REE abundances and patterns similar to those of Recent foraminifera from the Atlantic Ocean. Electron microprobe analyses (n=178) of transition elements in 29 Arctic Fe-Mn micronodules from five different stratigraphic intervals of Late Cenozoic sediment indicate that oxide accretion occurred as a result of hydrogenetic and diagenetic processes close to the sediment-seawater interface. Transition element ratios suggest that no oxide accretion occurred during transitions from oxic to suboxic diagenetic conditions. Only K is correlated with Si and Al, and ratios of these elements suggest that they are associated with illite or phillipsite. Ca and Mg are correlated with Mn, which indicates variable substitution of these elements from seawater into the manganate phase. The geochemical characteristics of Arctic Fe-Mn micronodules indicate that the REEs of the oxide fractions were ultimately derived from seawater. However, because of minute contributions of Sr from siliciclastic detritus during diagenesis or during the chemical leaching procedure, Sr isotope compositions of the oxide fractions cannot be used to trace temporal changes in the Sr-87/Sr-86 ratio of Arctic seawater or to improve the chronostratigraphy.
    Keywords: Alpha Ridge, Arctic Ocean; CESAR; CESAR_83-011; FL-275; FL-286; FL-380; FL-443; GC; Gravity corer; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Sampling/drilling from ice; Sampling/drilling ice; T-3
    Type: Dataset
    Format: application/zip, 4 datasets
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  • 6
    Publication Date: 2023-08-28
    Keywords: Alpha Ridge, Arctic Ocean; CESAR; CESAR_83-011; DEPTH, sediment/rock; Event label; FL-275; FL-286; FL-380; FL-443; GC; Geologic age name; Gravity corer; Identification; Insoluble residue; Mass; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Sampling/drilling from ice; Sampling/drilling ice; Soluble residue; T-3; Wet chemistry
    Type: Dataset
    Format: text/tab-separated-values, 78 data points
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  • 7
    Publication Date: 2023-08-28
    Keywords: Alpha Ridge, Arctic Ocean; CAMECA SX50 electron microprobe; Cerium; CESAR; CESAR_83-011; DEPTH, sediment/rock; Dysprosium; Erbium; Europium; Event label; FL-275; FL-286; FL-380; FL-443; Gadolinium; GC; Gravity corer; Identification; Mass spectrometer VG Sector 54; Neodymium; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Rubidium; Rubidium-87/Strontium-86 ratio; Samarium; Sampling/drilling from ice; Sampling/drilling ice; Strontium; Strontium-87/Strontium-86 ratio; Strontium-87/Strontium-86 ratio, error; T-3; Ytterbium
    Type: Dataset
    Format: text/tab-separated-values, 193 data points
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  • 8
    Publication Date: 2022-05-25
    Description: © The Author(s), 2017. This is the author's version of the work. It is posted here under a nonexclusive, irrevocable, paid-up, worldwide license granted to WHOI. It is made available for personal use, not for redistribution. The definitive version was published in Earth-Science Reviews 172 (2017): 140-177, doi:10.1016/j.earscirev.2017.06.012.
    Description: Iron formations (IF) represent an iron-rich rock type that typifies many Archaean and Proterozoic supracrustal successions and are chemical archives of Precambrian seawater chemistry and postdepositional iron cycling. Given that IF accumulated on the seafloor for over two billion years of Earth’s early history, changes in their chemical, mineralogical, and isotopic compositions offer a unique glimpse into environmental changes that took place on the evolving Earth. Perhaps one of the most significant events was the transition from an anoxic planet to one where oxygen was persistently present within the marine water column and atmosphere. Linked to this progressive global oxygenation was the evolution of aerobic microbial metabolisms that fundamentally influenced continental weathering processes, the supply of nutrients to the oceans, and, ultimately, diversification of the biosphere and complex life forms. Many of the key recent innovations in understanding IF genesis are linked to geobiology, since biologically assisted Fe(II) oxidation, either directly through photoferrotrophy, or indirectly through oxygenic photosynthesis, provides a process for IF deposition from mineral precursors. The abundance and isotope composition of Fe(II)-bearing minerals in IF additionally suggests microbial Fe(III) reduction, a metabolism that is deeply rooted in the Archaea and Bacteria. Linkages among geobiology, hydrothermal systems, and deposition of IF have been traditionally overlooked, but now form a coherent model for this unique rock type. This paper reviews the defining features of IF and their distribution through the Neoarchaean and Palaeoproterozoic. This paper is an update of previous reviews by Bekker et al. (2010, 2014) that will improve the quantitative framework we use to interpret IF deposition. In this work, we also discuss how recent discoveries have provided new insights into the processes underpinning the global rise in atmospheric oxygen and the geochemical evolution of the oceans.
    Description: KOK, TJW, RH, CAP and AB would like to thank the Natural Sciences and Engineering Research Council of Canada (NSERC) for its financial support. LJR gratefully acknowledges the support of a Vanier Canada Graduate Scholarship. CMJ, DSH, NJP and TWL acknowledge support from the NASA Astrobiology Institute. SVL acknowledges support from the European Institute for Marine Studies (LabexMER, ANR-10-LABX-19). HT and PBHO thank ASSMANG Ltd for providing research funding.
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
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  • 9
    ISSN: 1437-3262
    Keywords: Bohemian Massif ; Eclogites Geochronology ; Sr and Nd isotopes ; Mariánské Lázně Complex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The Mariánské Lázně complex (MLC) is located in the Bohemian Massif along the north-western margin of the Teplá-Barrandian microplate and consists of metagabbro, amphibolite and eclogite, with subordinate amounts of serpentinite, felsic gneiss and calcsilicate rocks. The MLC is interpreted as a metaophiolite complex that marks the suture zone between the Saxothuringian rocks to the north-west and the Teplá-Barrandian microplate to the south-east. Sm-Nd geochronology of garnet-omphacite pairs from two eclogite samples yields ages of 377±7, and 367±4 Ma. Samples of eclogite and amphibolite do not define a whole rock Sm-Nd isochron, even though there is a large range in Sm/Nd ratio, implying that the suite of samples may not be cogenetic. Eclogites do not have correlated ɛ Nd values and initial 87Sr/86Sr ratios. Five of the eight eclogite samples have high ɛ Nd values (+10.2 to +7.1) consistent with derivation from a MORB-like source, but variable 87Sr/86Sr ratios (0.7033 to 0.7059) which probably reflect hydrothermal seawater alteration. Three other eclogite samples have lower ɛNd values (+ 5.4 to −0.8) and widely variable 87Sr/86Sr ratios (0.7033 to 0.7096). Such low ɛNd values are inconsistent with derivation from a MORB, source and may reflect a subduction or oceanic island basalt component in their source. The MLC is an important petrotectonic element in the Bohemian Massif, providing evidence for Cambro-Ordovician formation of oceanic crust and interaction with seawater, Late Devonian (Frasnian-Famennian) high- and medium-pressure metamorphism related to closure of a Saxothuringian ocean basin, Early Carboniferous (Viséan) thrusting of the Teplá terrane over Saxothuringian rocks and Late Viséan extension.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0016-7835
    Keywords: Key words Bohemian Massif ; Eclogites ; Geochronology ; Sr and Nd isotopes ; Mariánské Lázně Complex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract  The Mariánské Lázně complex (MLC) is located in the Bohemian Massif along the north-western margin of the Teplá-Barrandian microplate and consists of metagabbro, amphibolite and eclogite, with subordinate amounts of serpentinite, felsic gneiss and calc-silicate rocks. The MLC is interpreted as a metaophiolite complex that marks the suture zone between the Saxothuringian rocks to the north-west and the Teplá-Barrandian microplate to the south-east. Sm-Nd geochronology of garnet-omphacite pairs from two eclogite samples yields ages of 377±7, and 367±4 Ma. Samples of eclogite and amphibolite do not define a whole rock Sm-Nd isochron, even though there is a large range in Sm/Nd ratio, implying that the suite of samples may not be cogenetic. Eclogites do not have correlated εNd values and initial 87Sr/86Sr ratios. Five of the eight eclogite samples have high εNd values (+10.2 to +7.1) consistent with derivation from a MORB-like source, but variable 87Sr/86Sr ratios (0.7033 to 0.7059) which probably reflect hydrothermal seawater alteration. Three other eclogite samples have lower εNd values (+5.4 to –0.8) and widely variable 87Sr/86Sr ratios (0.7033 to 0.7096). Such low εNd values are inconsistent with derivation from a MORB source and may reflect a subduction or oceanic island basalt component in their source. The MLC is an important petrotectonic element in the Bohemian Massif, providing evidence for Cambro-Ordovician formation of oceanic crust and interaction with seawater, Late Devonian (Frasnian-Famennian) high- and medium-pressure metamorphism related to closure of a Saxothuringian ocean basin, Early Carboniferous (Viséan) thrusting of the Teplá terrane over Saxothuringian rocks and Late Viséan extension.
    Type of Medium: Electronic Resource
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