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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
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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
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 92 (1988), S. 7193-7204 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 8971-8979 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The representation of the two-dimensional harmonic oscillator by the unitary group SU (2) simple Coriolis-adapted vibrational basis states for the treatment of vibration–rotation interaction in polyatomic molecules. The vibrational part of the zeroth-order vibration–rotation Hamiltonian is expressed in terms of the generators (Sx,Sy,Sz) of the group SU(2), leading to a coupled angular momentum representation of the vibration–rotation Hamiltonian. In the prolate limit, this leads to an effective k-dependent zeroth-order vibrational Hamiltonian that is linear in the group generators. The problem can be solved exactly in this limit by a simple axis transformation in the vibrational "spin'' space. Because of the underlying SU(2) structure, the transformation matrix elements and overlaps of basis states of different effective Hamiltonians corresponding to different values of k are given by simple expressions involving Wigner d matrices.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 3594-3606 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A coupled spin representation is introduced to describe the classical dynamics of two vibrational modes of a polyatomic molecule coupled by Coriolis interaction to overall molecular rotation. The mechanisms of Coriolis-induced periodic energy exchange between the vibrational modes, resonant vibration–rotation interaction, and chaotic energy transfer are described, and the dependence of the dynamics on rotational angular momentum, vibrational energy, total energy, and parameters in the Hamiltonian is explored using classical trajectory integrations and the surface of section method. The integrable motion occuring in the prolate limit is considered geometrically from the coupled spin representation, which provides clear insight into the dynamics of the system. In addition, this approach allows analytic results describing the effect of Coriolis coupling on vibration–rotation dynamics to be obtained.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 7234-7241 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The vibrational predissociation dynamics of an Ar13 cluster containing a vibrationally excited I2 molecule in its B electronic state are studied by classical trajectory simulation. The kinetics of the loss of the first Ar atom from the cluster induced by vibrational relaxation of the diatomic exhibits unusual nonexponential behavior, characterized by an instantaneous rate that increases with time. The simulation results are modeled by a hybrid statistical model, which explicitly takes into account the slow relaxation of the impurity while assuming rapid redistribution of energy among the low frequency cluster modes. Minor deviations between the simulation and theory are observed, and indicate nonstatistical effects in the "solvent'' degrees of freedom.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 1870-1885 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A qualitative method for visualizing vibration–rotation eigenstates of polyatomic molecules is described and applied to a "coupled spin'' model of Coriolis interaction of two nearly degenerate vibrations and molecular rotation. The method employs generalized coherent states of the Lie group SU(2)⊗SU(2) to define a quantum surface of section for coupled angular momentum problems. Stationary states of the vibration–rotation Hamiltonian are visualized on the rotational surface of section, and compared with the corresponding classical phase space structure. Striking classical-quantum correspondence is observed. The parallels between classical and quantum properties are investigated for several values of the total angular momentum, total number of vibrational quanta, and total energy. In addition, the evolution of classical and quantum mechanical phase space structure with variation of parameters in the Hamiltonian is studied.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 8805-8808 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Molecular dynamics investigation of a prototypical model reaction I–Arn(n=12)+I reveals the role of microscopic solvation in association reactions: (a) enhancement of capture cross section of the incident I atom; (b) mediation of the migration of I to form I2; and (c) stabilization of I2 product by evaporative cooling.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 5621-5633 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: This paper examines the effect of large amplitude internal rotation on the rate and extent of intramolecular vibrational energy redistribution (IVR). We study a classical Hamiltonian modeling the vibrations of p-fluorotoluene in its first excited singlet (S1) electronic state. We find that the full many-dimensional vibrational phase space of this system can be approximately decomposed into two subsystems. The first consists of the methyl rotor and the lowest-frequency ring modes, which interest strongly and chaotically with the methyl rotor. Within this subsystem, energy is rapidly exchanged. The second subsystem consists of the remaining high-frequency modes, which do not strongly couple to the methyl rotor directly. The chaotic low-frequency ring–rotor dynamics generate an effectively random force on the remaining degrees of freedom. This intrinsically stochastic perturbation induces slower intramolecular energy diffusion and relaxation of nonequilibrium initial distributions in the higher-frequency ring modes.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 2328-2337 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We examine the classical, semiclassical, and quantum mechanics of the Hamiltonian H= 1/2 (p2x+p2y+x2y2). The dynamics of this system are globally chaotic. However, the classical and quantum mechanical problems can be solved analytically by assuming an adiabatic separation of the x and y motion. We construct the canonical transformation to adiabatic action–angle variables and investigate the connection between this integrable approximation and the exact dynamics. In addition, we present a simple semiclassical formula that predicts energy levels in excellent agreement with the exact energy spectrum. The quantum adiabatic potential curves of this system have a very unusual structure—infinitely many curves cross at one point.
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