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  • 1
    Call number: 9/M 07.0113
    In: Memoir
    Type of Medium: Monograph available for loan
    Pages: 947 S. : Ill., graph. Darst.
    ISBN: 0920230008
    Series Statement: Memoir / Canadian Society of Petroleum Geologists 19
    Classification:
    Historical Geology
    Location: Reading room
    Branch Library: GFZ Library
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  • 2
    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
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  • 3
    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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  • 4
    ISBN: 9780444509673
    Language: English
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  • 5
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    PANGAEA
    In:  Supplement to: Henderson, Gideon M (2002): Seawater (234U/238U) during the last 800 thousand years. Earth and Planetary Science Letters, 199(1-2), 97-110, https://doi.org/10.1016/S0012-821X(02)00556-3
    Publication Date: 2024-02-03
    Description: Constraining the history of seawater (234U/238U) is important because this ratio is used to assess the validity of U/Th ages, and because it provides information about the past rate of physical weathering on the continents. This study makes use of U-rich slope sediments from the Bahamas in an attempt to reconstruct seawater (234U/238U) for the last 800 kyr. For the last 360 kyr, U/Th dating of these sediments provides ages and initial (234U/238U) values. Sixty-seven samples, largely from marine highstands, have initial (234U/238U) which scatter somewhat about the modern seawater value (~1.145) but neither this scatter nor the average value increases with age of sample. These data contrast with published coral data and suggest that seawater (234U/238U) has remained within 15‰ of the modern value for the last 360 kyr. This confirms the rejection of coral U/Th ages where the initial (234U/238U) is significantly different from modern seawater. Data from older highstands, dated with delta18O stratigraphy or by the presence of the Brunhes/Matuyama (B/M) reversal at 780 kyr, allow seawater (234U/238U) to be assessed prior to the range of the 230Th chronometer. Unfortunately, diagenetic scatter in the data between the B/M reversal and 360 kyr is rather large, probably relating to low U concentrations for these samples. But there is no indication of a trend in seawater (234U/238U) with age. High U samples from close to the B/M reversal show less diagenetic scatter and an initial (234U/238U) that averages 1.102. This lower value can be explained by lower seawater (234U/238U) at the time of the B/M reversal, or by progressive loss of 234U from the sediment by alpha-recoil. A simple box model is presented to illustrate the response of seawater (234U/238U) to variations in riverine input, such as might be caused by changes in continental weathering. Comparison of the Bahamas (234U/238U) data with model results indicates that riverine (234U/238U) has not varied by more than 65‰ for any 100 kyr period during the last 360 kyr. It also indicates that the ratio of physical to chemical weathering on the continents has not been higher than at present for any extended period during the last 800 kyr.
    Keywords: 166-1003; 166-1004A; 166-1005A; 166-1006; 166-1006A; 166-1008A; 166-1009A; COMPCORE; Composite Core; DRILL; Drilling/drill rig; Joides Resolution; Leg166; Ocean Drilling Program; ODP; South Atlantic Ocean
    Type: Dataset
    Format: application/zip, 4 datasets
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  • 6
    Publication Date: 2024-02-03
    Keywords: 166-1004A; AGE; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Joides Resolution; Leg166; Multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS); Ocean Drilling Program; ODP; Sample code/label; South Atlantic Ocean; Thorium-230/Thorium-232 activity ratio; Thorium-230/Thorium-232 activity ratio, standard deviation; Thorium-230/Uranium-234 activity ratio; Thorium-230/Uranium-234 activity ratio, standard deviation; Uranium; Uranium, standard deviation; δ234 Uranium; δ234 Uranium, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 70 data points
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  • 7
    Publication Date: 2024-02-03
    Keywords: 166-1006; AGE; Aragonite; COMPCORE; Composite Core; DEPTH, sediment/rock; DSDP/ODP/IODP sample designation; Joides Resolution; Leg166; Marine isotopic stage; Multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS); Ocean Drilling Program; ODP; Sample code/label; South Atlantic Ocean; Thorium-230/Thorium-232 activity ratio; Thorium-230/Thorium-232 activity ratio, standard deviation; Thorium-230/Uranium-234 activity ratio; Thorium-230/Uranium-234 activity ratio, standard deviation; Uranium; Uranium, standard deviation; δ234 Uranium; δ234 Uranium, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 320 data points
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  • 8
    Publication Date: 2024-03-09
    Keywords: 166-1009; Calcium carbonate; Calcium carbonate, standard deviation; Calculated; COMPCORE; Composite Core; DEPTH, sediment/rock; Description; DSDP/ODP/IODP sample designation; Electron microprobe (EMP); Iron; Iron, standard deviation; Joides Resolution; Leg166; Magnesium carbonate, magnesite; Manganese; Minerals; Number of observations; Ocean Drilling Program; ODP; Sample code/label; Sodium; Sodium, standard deviation; South Atlantic Ocean; Standard deviation; Strontium; Strontium, standard deviation; Sulfur, standard deviation; Sulfur, total
    Type: Dataset
    Format: text/tab-separated-values, 65 data points
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  • 9
    Publication Date: 2024-03-09
    Keywords: 166-1008; Aragonite; Calcite; Calcium; Calcium/Chlorine ratio; Calcium carbonate saturation; Calculated; COMPCORE; Composite Core; DEPTH, sediment/rock; Joides Resolution; Leg166; Magnesium/Chlorine ratio; Ocean Drilling Program; ODP; South Atlantic Ocean; Strontium/Chloride ratio; Sulfate; Sulfate/Chlorine ratio
    Type: Dataset
    Format: text/tab-separated-values, 140 data points
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  • 10
    Publication Date: 2024-03-09
    Keywords: 166-1009; Aragonite; Calcite; Calcium; Calcium/Chlorine ratio; Calcium carbonate saturation; Calculated; COMPCORE; Composite Core; DEPTH, sediment/rock; Joides Resolution; Leg166; Magnesium/Chlorine ratio; Ocean Drilling Program; ODP; South Atlantic Ocean; Strontium/Chloride ratio; Sulfate; Sulfate/Chlorine ratio
    Type: Dataset
    Format: text/tab-separated-values, 243 data points
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