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  • 1
    Series available for loan
    Series available for loan
    Washington, D.C. : Mineralogical Society of America
    Associated volumes
    Call number: 11/M 03.0180
    In: Reviews in mineralogy & geochemistry
    Description / Table of Contents: Exactly 100 years before the publication of this volume, the first paper which calculated the half-life for the newly discovered radioactive substance U-X (now called 234Th), was published. Now, in this volume, the editors Bernard Bourdon, Gideon Henderson, Craig Lundstrom and Simon Turner have integrated a group of contributors who update our knowledge of U-series geochemistry, offer an opportunity for non-specialists to understand its basic principles, and give us a view of the future of this active field of research. In this volume, for the first time, all the methods for determining the uranium and thorium decay chain nuclides in Earth materials are discussed. It was prepared in advance of a two-day short course (April 3-4, 2003) on U-series geochemistry, jointly sponsored by GS and MSA and presented in Paris, France prior to the joint EGS/AGU/EUG meeting in Nice. The discovery of the 238U decay chain, of course, started with the seminal work of Marie Curie in identifying and separating 226Ra. Through the work of the Curies and others, all the members of the 238U decay chain were identified. An important milestone for geochronometrists was the discovery of 230Th (called Ionium) by Bertram Boltwood, the Yale scientist who also made the first age determinations on minerals using the U-Pb dating method (Boltwood in 1906 established the antiquity of rocks and even identified a mineral from Sri Lanka-then Ceylon as having an age of 2.1 billion years!) The application of the 238U decay chain to the dating of deep sea sediments was by Piggott and Urry in 1942 using the "Ionium" method of dating. Actually they measured 222Ra (itself through 222Rn) assuming secular equilibrium had been established between 230Th and 226Ra. Although 230Th was measured in deep sea sediments by Picciotto and Gilvain in 1954 using photographic emulsions, it was not until alpha spectrometry was developed in the late 1950's that 20Th was routinely measured in marine deposits. Alpha spectrometry and gamma spectrometry became the work horses for the study of the uranium and thorium decay chains in a variety of Earth materials. These ranged from 222Rn and its daughters in the atmosphere, to the uranium decay chain nuclides in the oceanic water column, and volcanic rocks and many other systems in which either chronometry or element partitioning, were explored. Much of what we learned about the 238U, 235U and 232Th decay chain nuclides as chronometers and process indicators we owe to these seminal studies based on the measurement of radioactivity. The discovery that mass spectrometry would soon usurp many of the tasks performed by radioactive counting was in itself serendipitous. It came about because a fundamental issue in cosmochemistry was at stake. Although variation in 235U/238U had been reported for meteorites the results were easily discredited as due to analytical difficulties. One set of results, however, was published by a credible laboratory long involved in quality measurements of high mass isotopes such as the lead isotopes. The purported discovery of 235U/238U variations in meteorites, if true, would have consequences in defining the early history of the formation of the elements and the development of inhomogeneity of uranium isotopes in the accumulation of the protoplanetary materials of the Solar System. Clearly the result was too important to escape the scrutiny of falsification implicit in the way we do science. The Lunatic Asylum at Caltech under the leadership of Jerry Wasserburg took on that task. Jerry Wasserburg and Jim Chen clearly established the constancy and Earth-likeness of 235U/238U in the samplable universe. In the hands of another member of the Lunatic Asylum, Larry Edwards, the methodology was transformed into a tool for the study of the 238U decay chain in marine systems. Thus the mass spectrometric techniques developed provided an approach to measuring the U and Th isotopes in geological materials as well as cosmic materials with the same refinement and accommodation for small sample size. Soon after this discovery the harnessing of the technique to the measurement of all the U isotopes and all the Th isotopes with great precision immediately opened up the entire field of uranium and thorium decay chain studies. This area of study was formerly the poaching ground for radioactive measurements alone but now became part of the wonderful world of mass spectrometric measurements. (The same transformation took place for radiocarbon from the various radioactive counting schemes to 'accelerator mass spectrometry.) No Earth material was protected from this assault. The refinement of dating corals, analyzing volcanic rocks for partitioning and chronometer studies and extensions far and wide into ground waters and ocean bottom dwelling organisms has been the consequence of this innovation. Although Ra isotopes, 210Pb and 210Po remain an active pursuit of those doing radioactive measurements, many of these nuclides have also become subject to the mass spectrometric approach. In this volume, for the first time, all the methods for determining the uranium and thorium decay chain nuclides in Earth materials are discussed. The range of problems solvable with this approach is remarkable-a fitting, tribute to the Curies and the early workers who discovered them for us to use.
    Type of Medium: Series available for loan
    Pages: xx, 656 S.
    ISBN: 0-939950-64-2 , 978-0-939950-64-5
    ISSN: 1529-6466
    Series Statement: Reviews in mineralogy & geochemistry 52
    Classification:
    Geochemistry
    Language: English
    Note: Chapter 1. Introduction to U-series Geochemistry by Bernard Bourdon, Simon Turner, Gideon M. Henderson and Craig C. Lundstrom, p. 1 - 22 Chapter 2. Techniques for Measuring Uranium-series Nuclides: 1992-2002 by Steven J. Goldstein and Claudine H. Stirling, p. 23 - 58 Chapter 3. Mineral-Melt Partitioning of Uranium, Thorium and Their Daughters by Jonathan Blundy and Bernard Wood, p. 59 - 124 Chapter 4. Timescales of Magma Chamber Processes and Dating of Young Volcanic Rocks by Michel Condomines, Pierre-Jean Gauthier, and Olgeir Sigmarsson, p. 125 - 174 Chapter 5. Uranium-series Disequilibria in Mid-ocean Ridge Basalts: Observations and Models of Basalt Genesis by Craig C. Lundstrom, p. 175 - 214 Chapter 6. U-series Constraints on Intraplate Basaltic Magmatism by Bernard Bourdon and Kenneth W. W. Sims, p. 215 - 254 Chapter 7. Insights into Magma Genesis at Convergent Margins from U-series Isotopes by Simon Turner, Bernard Bourdon and Jim Gill, p. 255 - 316 Chapter 8. The Behavior of U- and Th-series Nuclides in Groundwater by Donald Porcelli and Peter W. Swarzenski, p. 317 - 362 Chapter 9. Uranium-series Dating of Marine and Lacustrine Carbonates by R. L. Edwards, C. D. Gallup, and H. Cheng, p. 363 - 406 Chapter 10. Uranium-series Chronology and Environmental Applications of Speleothems by David A. Richards and Jeffrey A. Dorale, p. 407 - 460 Chapter 11. Short-lived U/Th Series Radionuclides in the Ocean: Tracers for Scavenging Rates, Export Fluxes and Particle Dynamics by J. K. Cochran and P. Masquè, p. 461 - 492 Chapter 12. The U-series Toolbox for Paleoceanography by Gideon M. Henderson and Robert F. Anderson, p. 493 - 532 Chapter 13. U-Th-Ra Fractionation During Weathering and River Transport by F. Chabaux, J. Riotte and O. Dequincey, p. 533 - 576 Chapter 14. The Behavior of U- and Th-series Nuclides in the Estuarine Environment by Peter W. Swarzenski, Donald Porcelli, Per S. Andersson and Joseph M. Smoakv, p. 577 - 606 Chapter 15. U-series Dating and Human Evolution by A. W. G. Pike and P. B. Pettitt, p. 607 - 630 Chapter 16. Mathematical-Statistical Treatment of Data and Errors for 230Th/U Geochronology by K. R. Ludwig, p. 631 - 656
    Location: Reading room
    Branch Library: GFZ Library
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  • 2
    Description / Table of Contents: Exactly 100 years before the publication of this volume, the first paper which calculated the half-life for the newly discovered radioactive substance U-X (now called 234Th), was published. Now, in this volume, the editors Bernard Bourdon, Gideon Henderson, Craig Lundstrom and Simon Turner have integrated a group of contributors who update our knowledge of U-series geochemistry, offer an opportunity for non-specialists to understand its basic principles, and give us a view of the future of this active field of research. In this volume, for the first time, all the methods for determining the uranium and thorium decay chain nuclides in Earth materials are discussed. It was prepared in advance of a two-day short course (April 3-4, 2003) on U-series geochemistry, jointly sponsored by GS and MSA and presented in Paris, France prior to the joint EGS/AGU/EUG meeting in Nice. The discovery of the 238U decay chain, of course, started with the seminal work of Marie Curie in identifying and separating 226Ra. Through the work of the Curies and others, all the members of the 238U decay chain were identified. An important milestone for geochronometrists was the discovery of 230Th (called Ionium) by Bertram Boltwood, the Yale scientist who also made the first age determinations on minerals using the U-Pb dating method (Boltwood in 1906 established the antiquity of rocks and even identified a mineral from Sri Lanka-then Ceylon as having an age of 2.1 billion years!) The application of the 238U decay chain to the dating of deep sea sediments was by Piggott and Urry in 1942 using the "Ionium" method of dating. Actually they measured 222Ra (itself through 222Rn) assuming secular equilibrium had been established between 230Th and 226Ra. Although 230Th was measured in deep sea sediments by Picciotto and Gilvain in 1954 using photographic emulsions, it was not until alpha spectrometry was developed in the late 1950's that 20Th was routinely measured in marine deposits. Alpha spectrometry and gamma spectrometry became the work horses for the study of the uranium and thorium decay chains in a variety of Earth materials. These ranged from 222Rn and its daughters in the atmosphere, to the uranium decay chain nuclides in the oceanic water column, and volcanic rocks and many other systems in which either chronometry or element partitioning, were explored. Much of what we learned about the 238U, 235U and 232Th decay chain nuclides as chronometers and process indicators we owe to these seminal studies based on the measurement of radioactivity. The discovery that mass spectrometry would soon usurp many of the tasks performed by radioactive counting was in itself serendipitous. It came about because a fundamental issue in cosmochemistry was at stake. Although variation in 235U/238U had been reported for meteorites the results were easily discredited as due to analytical difficulties. One set of results, however, was published by a credible laboratory long involved in quality measurements of high mass isotopes such as the lead isotopes. The purported discovery of 235U/238U variations in meteorites, if true, would have consequences in defining the early history of the formation of the elements and the development of inhomogeneity of uranium isotopes in the accumulation of the protoplanetary materials of the Solar System. Clearly the result was too important to escape the scrutiny of falsification implicit in the way we do science. The Lunatic Asylum at Caltech under the leadership of Jerry Wasserburg took on that task. Jerry Wasserburg and Jim Chen clearly established the constancy and Earth-likeness of 235U/238U in the samplable universe. In the hands of another member of the Lunatic Asylum, Larry Edwards, the methodology was transformed into a tool for the study of the 238U decay chain in marine systems. Thus the mass spectrometric techniques developed provided an approach to measuring the U and Th isotopes in geological materials as well as cosmic materials with the same refinement and accommodation for small sample size. Soon after this discovery the harnessing of the technique to the measurement of all the U isotopes and all the Th isotopes with great precision immediately opened up the entire field of uranium and thorium decay chain studies. This area of study was formerly the poaching ground for radioactive measurements alone but now became part of the wonderful world of mass spectrometric measurements. (The same transformation took place for radiocarbon from the various radioactive counting schemes to accelerator mass spectrometry.) No Earth material was protected from this assault. The refinement of dating corals, analyzing volcanic rocks for partitioning and chronometer studies and extensions far and wide into ground waters and ocean bottom dwelling organisms has been the consequence of this innovation. Although Ra isotopes, 210Pb and 210Po remain an active pursuit of those doing radioactive measurements, many of these nuclides have also become subject to the mass spectrometric approach. In this volume, for the first time, all the methods for determining the uranium and thorium decay chain nuclides in Earth materials are discussed. The range of problems solvable with this approach is remarkable-a fitting, tribute to the Curies and the early workers who discovered them for us to use.
    Pages: Online-Ressource (XX, 656 Seiten)
    ISBN: 0939950642
    Language: English
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  • 3
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Thomas, Alexander L; Henderson, Gideon M; McCave, I Nick (2007): Constant bottom water flow into the Indian Ocean for the past 140 ka indicated by sediment 231PAPa/230Th ratios. Paleoceanography, 22(4), PA4210, https://doi.org/10.1029/2007PA001415
    Publication Date: 2023-05-12
    Description: A down-core 231Pa/230Th record has been measured from the southwestern Indian Ocean to reconstruct the history of deep water flow into this basin over the last glacial-interglacial cycle. The (231Paxs/230Thxs)0 ratio throughout the record is nearly constant at approximately 0.055, significantly lower than the production ratio of 0.093, indicating that the proxy is sensitive to changes in circulation and/or sediment flux at this site. The consistent value suggests that there has been no change in the inflow of Antarctic Bottom Water to the Indian Ocean during the last 140 ka, in contrast to the changes in deep circulation thought to occur in other ocean basins. The stability of the (231Paxs/230Thxs)0 value in the record contrasts with an existing sortable silt (SS) record from the same core. The observed equation image variability is attributed to a local geostrophic effect amplifying small changes in circulation. A record of authigenic U from the same core suggests that there was reduced oxygen in bottom waters at the core locality during glacial periods. The consistency of the (231Paxs/230Thxs)0 record implies that this could not have arisen by local changes in productivity, thus suggesting a far-field control: either globally reduced bottom water oxygenation or increased productivity south of the Opal Belt during glacials.
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 4
    Publication Date: 2023-05-12
    Keywords: Coppitella; Inductively coupled plasma - mass spectrometry (ICP-MS); Italy; OUTCROP; Outcrop sample; SECTION, height; δ44/40 Ca; δ44/40 Ca, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 40 data points
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  • 5
    Publication Date: 2023-06-27
    Keywords: AGE; Calculated; DEPTH, sediment/rock; Mass spectrometer VG Sector 354 multicollector; PC; Piston corer; RC14; RC14-37; Robert Conrad; Sample comment; Standard deviation; Strontium-87/Strontium-86 ratio; Strontium-87/Strontium-86 ratio, error; Δ87Sr
    Type: Dataset
    Format: text/tab-separated-values, 20 data points
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  • 6
    Publication Date: 2023-06-27
    Keywords: AGE; Calculated; DEPTH, sediment/rock; Mass spectrometer VG Sector 354 multicollector; PC; Piston corer; RC17; RC17-177; Robert Conrad; Sample comment; Standard deviation; Strontium-87/Strontium-86 ratio; Strontium-87/Strontium-86 ratio, error; Δ87Sr
    Type: Dataset
    Format: text/tab-separated-values, 30 data points
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  • 7
    Publication Date: 2023-06-27
    Keywords: AGE; Calculated; DEPTH, sediment/rock; Mass spectrometer VG Sector 354 multicollector; PC; Piston corer; Sample comment; Standard deviation; Strontium-87/Strontium-86 ratio; Strontium-87/Strontium-86 ratio, error; V28; V28-238; Vema; Δ87Sr
    Type: Dataset
    Format: text/tab-separated-values, 95 data points
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  • 8
    Publication Date: 2023-05-12
    Keywords: Inductively coupled plasma - mass spectrometry (ICP-MS); OUTCROP; Outcrop sample; SECTION, height; South_Ferriby; United Kingdom; δ13C, carbonate; δ44/40 Ca; δ44/40 Ca, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 73 data points
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  • 9
    Publication Date: 2023-05-12
    Keywords: Eastbourne; Inductively coupled plasma - mass spectrometry (ICP-MS); OUTCROP; Outcrop sample; SECTION, height; United Kingdom; δ44/40 Ca; δ44/40 Ca, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 56 data points
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  • 10
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Jonkers, Lukas; Zahn, Rainer; Thomas, Alexander; Henderson, Gideon M; Abouchami, Wafa; Francois, Roger; Masqué, Pere; Hall, Ian R; Bickert, Torsten (2015): Deep circulation changes in the central South Atlantic during the past 145 kyrs reflected in a combined 231Pa/230Th, Neodymium isotope and benthic d13C record. Earth and Planetary Science Letters, 419, 14-21, https://doi.org/10.1016/j.epsl.2015.03.004
    Publication Date: 2023-07-05
    Description: Previous work showed that South Atlantic sediments have lower glacial than Holocene 231Pa/230Th, which was attributed to a switch in the flow direction of Atlantic deep-water. Debate exists, however as to the degree to which two processes - circulation and scavenging - determine sedimentary 231Pa/230Th, making this interpretation contentious. Here we address this issue using 145-kyr records of paleocirculation proxies. Benthic foraminiferal d13C, neodymium isotopes (ENd) and sedimentary 231Pa/230Th were all measured in a single sediment core from the South Atlantic subtropical gyre. This site largely excludes the influence of local productivity changes on 231Pa/230Th records. Measured 231Pa/230Th ranges between ~0.041 during glacials to ~0.055 during interglacial periods and are consistently lower than the production ratio, indicating export of 231Pa from the central South Atlantic for the entire duration of the record. The lower glacial 231Pa/230Th is regionally consistent, suggesting that basin-scale oceanographic processes cause the decrease. In turn, less radiogenic ENd and lower benthic d13C confirm the classical picture of an increase in Southern Component Water (SCW) influence in the Atlantic during glacial periods and point to a circulation control on the observed 231Pa/230Th decrease rather than a local productivity change. We suggest that associated with this change in water mass distribution the dominant sink for 231Pa shifted from the margins of the South Atlantic and/or the Southern Ocean during interglacials, to the North Atlantic during glacial periods. Indeed, elevated 231Pa/230Th in the deep North Atlantic during glacials supports this mechanism of northward transport of 231Pa by SCW.
    Keywords: Center for Marine Environmental Sciences; GeoB; Geosciences, University of Bremen; MARUM
    Type: Dataset
    Format: application/zip, 3 datasets
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