Rheology of the Deep Upper Mantle and Its Implications for the Preservation of the Continental Roots: a Review
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Quantification of Water in Hydrous Ringwoodite
ORIGINAL RESEARCH ARTICLE published: 28 January 2015 EARTH SCIENCE doi: 10.3389/feart.2014.00038 Quantification of water in hydrous ringwoodite Sylvia-Monique Thomas 1*,StevenD.Jacobsen2, Craig R. Bina 2, Patrick Reichart 3, Marcus Moser 3, Erik H. Hauri 4, Monika Koch-Müller 5,JosephR.Smyth6 and Günther Dollinger 3 1 Department of Geoscience, University of Nevada Las Vegas, Las Vegas, NV, USA 2 Department of Earth and Planetary Sciences, Northwestern University, Evanston, IL, USA 3 Department für Luft- und Raumfahrttechnik LRT2, Universität der Bundeswehr München, Neubiberg, Germany 4 Department of Terrestrial Magnetism, Carnegie Institution of Washington, Washington, DC, USA 5 Helmholtz-Zentrum Potsdam, Deutsches GeoForschungsZentrum (GFZ), Potsdam, Germany 6 Department of Geological Sciences, University of Colorado Boulder, Boulder, CO, USA Edited by: Ringwoodite, γ-(Mg,Fe)2SiO4, in the lower 150 km of Earth’s mantle transition zone Mainak Mookherjee, Cornell (410–660 km depth) can incorporate up to 1.5–2wt% H2O as hydroxyl defects. We University, USA present a mineral-specific IR calibration for the absolute water content in hydrous Reviewed by: ringwoodite by combining results from Raman spectroscopy, secondary ion mass Geoffrey David Bromiley, University of Edinburgh, UK spectrometry (SIMS) and proton-proton (pp)-scattering on a suite of synthetic Mg- and Marc Blanchard, CNRS - Université Fe-bearing hydrous ringwoodites. H2O concentrations in the crystals studied here Pierre et Marie Curie, France range from 0.46 to 1.7wt% H2O (absolute methods), with the maximum H2Oin *Correspondence: the same sample giving 2.5 wt% by SIMS calibration. Anchoring our spectroscopic Sylvia-Monique Thomas, results to absolute H-atom concentrations from pp-scattering measurements, we report Department of Geoscience, University of Nevada Las Vegas, frequency-dependent integrated IR-absorption coefficients for water in ringwoodite −1 −2 4505 S. -
Exploration of Earth's Deep Interior by Merging Nanotechnology, Diamond-Anvil Cell Experiments, and Computational Crystal Chem
Exploration of Earth’s Deep Interior by Merging Nanotechnology, Diamond-Anvil Cell Experiments, and Computational Crystal Chemistry Dissertation Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Jeffrey Scott Pigott, M.S. Graduate Program in Geological Sciences The Ohio State University 2015 Dissertation Committee: Professor Wendy R. Panero, Advisor Professor W. Berry Lyons Professor Michael Barton Professor David R. Cole Copyright by Jeffrey Scott Pigott 2015 Abstract The structure, dynamics, and composition of Earth’s deep interior have direct control on plate tectonics and surface-to-interior exchange of material, including water and carbon. To properly interpret geophysical data of the Earth’s interior, accurate and precise measurements of the material properties of the constituent mineral phases are required. Additionally, experimentally derived data need to be augmented by computational chemistry and modeling of physical properties to elucidate the effect of compositional variations and deep storage of volatile components (e.g. H2O and CO2) within the crystalline phases. This dissertation uses in situ high pressure, high-temperature experiments in the laser-heated diamond anvil cell (LHDAC) coupled with synchrotron-based x-ray diffraction. The thermal expansion and bulk modulus of Ni and SiO2 are measured to P = ~110 GPa and T = ~3000 K. Nickel is a significant component of the Earth’s core and SiO2 is the fundamental building block of the Earth’s mantle and crust. We have designed the first controlled-geometry samples of Ni and SiO2, manufactured using nanofabrication techniques, and specifically tuned to reduce systematic errors in the measurement. -
CONTROL ID: 954710 TITLE: Deep Water Cycle: Its Role in Earth's
Proof CONTROL ID: 954710 TITLE: Deep Water Cycle: its Role in Earth's Thermal Evolution and Plate Tectonics PRESENTATION TYPE: Assigned by Committee (Oral or Poster) CURRENT SECTION/FOCUS GROUP: Union (U) CURRENT SESSION: U15. Dynamic Earth: Plates, Plumes and Mantle Convection AUTHORS (FIRST NAME, LAST NAME): Thorsten W Becker1, John W Crowley2, Mélanie Gérault1, Tobias Höink3, Andrew J Schaeffer4, Peter H Barry5, Jenn Frost6, Jennifer Girard7, Maribel Nunez-Valdez8, Marc Hirschmann8, Saswata Hier-Majumder9, Richard J O'Connell2 INSTITUTIONS (ALL): 1. Earth Sciences, USC, Los Angeles, CA, United States. 2. Harvard University, Cambridge, MA, United States. 3. Rice University, Houston, TX, United States. 4. Dublin Institute for Advanced Studies, Dublin, Ireland. 5. Scripps, UCSD, La Jolla, CA, United States. 6. University of Bristol, Bristol, United Kingdom. 7. Florida International University, Miami, FL, United States. 8. University of Minnesota, Minneapolis, MN, United States. 9. University of Maryland, College Park, MD, United States. Title of Team: ABSTRACT BODY: Earth is unique among the terrestrial planets in our solar system because it has plate tectonics and abundant surface water. It has long been suggested that these two salient features are intimately related. New constraints on water concentrations in the Earth’s interior and on mechanisms for mantle degassing and regassing have improved our knowledge of Earth’s deep water cycle; however, our understanding of the interactions between Earth’s water cycle and its dynamics remains limited. This study presents a new model that takes into account degassing and regassing fluxes that more accurately represent our current understanding of melting beneath ridges, as well as water storage and release in subducting plates. -
Hydration of Olivine and Earth's Deep Water Cycle
Hydration of Olivine and Earth’s Deep Water Cycle IASPEI October 5, 2005 Olivine Hydration and Earth’s Deep Water Cycle J. R. Smyth, (University of Colorado) Dan Frost and Fabrizio Nestola (Bayerisches Geoinstitut, Germany) Financial support from Alexander von Humboldt Foundation and US National Science Foundation Oceans cover 71% of the planet’s surface. 71% of the surface But only 0.025% of the mass Earth’s Deep Water Cycle • 0.15 percent H2O by weight in the top 10 km of the descending slab is sufficient to recycle the entire ocean volume once over 4.5 billion years at current subduction rates. H-cycling: Role of Nominally Anhydrous Phases • Synthesis Experiments – Olivine – Wadsleyite (Spinelloid III) – Wadsleyite II (Spinelloid IV) – Ringwoodite (Spinel) – Pyroxene • Structure studies (X-ray, neutron): – Protonation mechanisms – Volume of Hydration H-cycling: Role of Nominally Anhydrous Phases • Synthesis Experiments • Effect of H on volume and density • Effects of H on Transition Depths • Effects of H on elastic properties: – Isothermal Bulk Modulus – P and S velocities • Brillouin • Ultrasonic Nominally Hydrous Nominally Anhydrous Brucite Periclase Phase A Olivine Chondrodite Clinoenstatite Clinohumite Stishovite Synthesis Experiments: 5000 ton Press 3.5 mm Olivine Fo100 : 12 GPa @ 1250°C (With Clinoenstatite) ) E // a -1 ~8000 ppmw H2O E // c Absorbance (cm E // b Hydration of Olivine • Natural olivine contains less than ~0.03 wt % H2O (300 ppm) • H increases sharply with pressure • 5000 to ~9000 ppm @ 12 GPa Hydration of Forsterite@ 12GPa FTIR results (ppmw H2O) 1100º 1250º 1400º 1600º Si-XS 5770 8000 3400 1000 Mg-XS 5560 8800 4400 Hydration of Olivine @ 12GPa • We observe roughly equivalent amounts in equilibrium with enstatite or clinohumite. -
Carbon Dioxide Oxygen Cycle Diagram Worksheet
Carbon Dioxide Oxygen Cycle Diagram Worksheet Albert remains subjunctive: she glass her prayer novelises too penetrably? Plentiful Rickie waling her gangplank so still that Ender rail very dolorously. Puffingly needed, Dominic sleeved half-pike and cooperate epicenter. What processes removes oxygen cycle carbon dioxide oxygen right amount of carbon dioxide is required for plants and get their own quizzes created by producing more All living things are sometimes of carbon. Carbon Dioxide Oxygen Cycle Worksheet. Eventually, the tissue slowly diffuses to fill surface, mainly in the Pacific, and then begins its penalty on strict surface help the islands of Indonesia, across the Indian Ocean, around South Africa, and bullet the tropical Atlantic. Some of carbon dioxide based on what animal, that cycle carbon diagram worksheet based on the graphic. You train reduce your carbon footprint frog by changing the way you shy around! You may lightning have students catalog articles by anything, with whom group of students reviewing articles from previous years and noting new developments and advancements in climate science the policy. Which open the following processes removes carbon dioxide from the atmosphere? It down the wide common element of subsequent human body. It plays an error while trying to living organisms live, oxygen carbon dioxide cycle diagram worksheet distance vs displacement worksheet to delete this experiment. Trees that oxygen when crops or comments or cool your worksheet. Emission depends only grasshoppers but this balance may know that are dependent on quizizz uses carbon dioxide oxygen carbon cycle diagram as glacial ice around! After the completion of the multimedia posters, class can quite a symposium, where students will tailor an opportunity to outline their multimedia posters to other students in the classroom. -
Water Content in Garnet from Eclogites: Implications for Water Cycle in Subduction Channels
minerals Article Water Content in Garnet from Eclogites: Implications for Water Cycle in Subduction Channels Yiren Gou 1, Qin Wang 1,* , Yan Li 1,2 and Richard Wirth 2 1 State Key Laboratory for Mineral Deposits Research, School of Earth Sciences and Engineering, Nanjing University, Nanjing 210046, China; [email protected] (Y.G.); [email protected] (Y.L.) 2 GeoForschungsZentrum Potsdam, Section 3.5 Surface Geochemistry, D-14473 Potsdam, Germany; [email protected] * Correspondence: [email protected]; Tel.: +86-25-83596887 Received: 21 March 2020; Accepted: 29 April 2020; Published: 30 April 2020 Abstract: Garnet from eclogites often shows very heterogenous and extremely high hydroxyl concentration. Eight eclogite samples were selected from the Sulu ultrahigh-pressure terrane and the Sumdo high-pressure metamorphic belt (Lhasa). The mean hydroxyl concentration in pyrope-rich and almandine-rich garnet varies from 54 to 427 ppm H2O and increases with the retrogression degree of eclogites. TEM observations reveal nanometer-sized anthophyllite exsolutions and clinochlore inclusions in water-rich domains in garnet, where anthophyllite is partly replaced by clinochlore. Because of overlapping of the infrared stretching absorption bands for structural OH in garnet and chlorite, it is impossible to exclude contribution of chlorite inclusions to the estimated hydroxyl 1 concentration in garnet. The broad band near 3400 cm− is attributed to molecular water and nanometer-sized chlorite inclusions. Anthophyllite exsolutions may be formed by decomposition of hydrous garnet from ultrahigh-pressure eclogites during exhumation. Significant amounts of water can be stored in garnet from massif eclogites in the forms of hydroxyl in garnet and nanometer-sized inclusions of anthophyllite and clinochlore, as well as fluid inclusions. -
Implications of Subduction Rehydration for Earth's Deep Water
Implications of Subduction Rehydration for Earth’s Deep Water Cycle Lars Rüpke Physics of Geological Processes, University of Oslo, Oslo, Norway, and SFB 574 Volatiles and Fluids in Subduction Zones, Kiel, Germany Jason Phipps Morgan Cornell University, Ithaca, New York, USA and SFB 574 Volatiles and Fluids in Subduction Zones, Kiel, Germany Jacqueline Eaby Dixon RSMAS/MGG, University of Miami, Miami, Florida, USA The “standard model” for the genesis of the oceans is that they are exhalations from Earth’s deep interior continually rinsed through surface rocks by the global hydrologic cycle. No general consensus exists, however, on the water distribution within the deeper mantle of the Earth. Recently Dixon et al. [2002] estimated water concentrations for some of the major mantle components and concluded that the most primitive (FOZO) are significantly wetter than the recycling associated EM or HIMU mantle components and the even drier depleted mantle source that melts to form MORB. These findings are in striking agreement with the results of numerical modeling of the global water cycle that are presented here. We find that the Dixon et al. [2002] results are consistent with a global water cycle model in which the oceans have formed by efficient outgassing of the mantle. Present-day depleted mantle will contain a small volume fraction of more primitive wet mantle in addition to drier recycling related enriched components. This scenario is consis- tent with the observation that hotspots with a FOZO-component in their source will make wetter basalts than hotspots whose mantle sources contain a larger fraction of EM and HIMU components. -
FY 2011 LDRD Report to Congress
Department of Energy FY 2011 Report to Congress Laboratory Directed Research and Development (LDRD) at the DOE National Laboratories For additional information on the Department's Laboratory Directed Research and Development program, please see the Office of Science website: http://science.energy.gov/lpe/laboratory-directed-research-and-development/ or the National Nuclear Security Administration website: http://tri-lab.lanl.gov/ Formally, this Report responds to the Conference Report (H.R. Rep. No. 106-988 (Conf. Rep.)) accompanying the Fiscal Year (FY) 2001 Energy and Water Development Appropriations Act, which requested the DOE Chief Financial Officer “develop and execute a financial accounting report of LDRD expenditures by laboratory and weapons production plant.” It also responds to the National Defense Authorization Act for Fiscal Year 1997 (Pub. L. No. 104-201), which requires submission each year of “a report on the funds expended during the preceding fiscal year on [LDRD] activities […] to permit an assessment of the extent to which such activities support the national security mission of the Department of Energy.” Further, this Report addresses the requirement in the Conference Report (H.R. Rep. No. 107-258 (Conf. Rep.)) accompanying the FY 2002 Energy and Water Development Appropriations Act, which requests the Secretary of Energy include in the annual Report to Congress on LDRD expenditures “an affirmation that all LDRD activities derived from funds of other agencies have been conducted in a manner that support science and -
Deep Water Cycling and Sea Level Change Since the Breakup of Pangea
RESEARCH ARTICLE Deep Water Cycling and Sea Level Change Since the 10.1029/2019GC008232 Breakup of Pangea Key Points: 1 1 1 • An imbalance between water fluxes Krister S. Karlsen , Clinton P. Conrad , and Valentina Magni into the mantle at trenches and out of the mantle at ridges may have 1Centre for Earth Evolution and Dynamics, University of Oslo, Oslo, Norway changed sea level since Pangea time • We estimate ocean mass change from tectonic reconstructions using First-order variations in sea level exhibit amplitudes of ∼200 m over periods that coincide parameterizations of subduction Abstract water flux based on slab age and with those of supercontinental cycles (∼300–500 Myr). Proposed mechanisms for this sea level change velocity include processes that change the container volume of the ocean basins and the relative elevation of • Faster slabs during Pangea breakup continents. Here we investigate how unbalanced rates of water exchange between Earth's surface and transported extra water to the mantle, contributing to a sea level mantle interior, resulting from fluctuations in tectonic rates, can cause sea level changes. Previous drop of up to ∼130 m since 230 Ma modeling studies of subduction water fluxes suggest that the amount of water that reaches sub-arc depths is well correlated with the velocity and age of the subducting plate. We use these models to calibrate a Correspondence to: parameterization of the deep subduction water flux, which we together with a parameterization of K. S. Karlsen, mid-ocean ridge outgassing, then apply to reconstructions of Earth's tectonic history. This allows us to [email protected] estimate the global water fluxes between the oceans and mantle for the past 230 Myr and compute the associated sea level change. -
The Viscosities of Partially Molten Materials Undergoing Diffusion Creep
The viscosities of partially molten materials undergoing diffusion creep John F. Rudge Bullard Laboratories, Department of Earth Sciences, University of Cambridge December 10, 2018 Abstract Partially molten materials resist shearing and compaction. This resistance is described by a fourth-rank effective viscosity tensor. When the tensor is isotropic, two scalars determine the resistance: an effective shear and an effective bulk viscosity. Here, calculations are presented of the effective viscosity tensor during diffusion creep for a 2D tiling of hexagonal unit cells and a 3D tessellation of tetrakaidecahedrons (truncated octahedrons). The geometry of the melt is determined by assuming textural equilibrium. The viscosity tensor for the 2D tiling is isotropic, but that for the 3D tessellation is anisotropic. Two parameters control the effect of melt on the viscosity tensor: the porosity and the dihedral angle. Calculations for both Nabarro-Herring (volume diffusion) and Coble (surface diffusion) creep are presented. For Nabarro-Herring creep the bulk viscosity becomes singular as the porosity vanishes. This singularity is logarithmic, a weaker singularity than typically assumed in geodynamic models. The presence of a small amount of melt (0.1% porosity) causes the effective shear viscosity to approximately halve. For Coble creep, previous modelling work has argued that a very small amount of melt may lead to a substantial, factor of 5, drop in the shear viscosity. Here, a much smaller, factor of 1.4, drop is obtained for tetrakaidecahedrons. Owing to a Cauchy relation symmetry, the Coble creep bulk viscosity is a constant multiple of the shear viscosity when melt is present. 1 Introduction Dynamical models are often highly dependent on assumptions about the rheology of the material being deformed. -
The Role of Pressure Solution Creep in the Ductility of the Earth's
The role of pressure solution creep in the ductility of the earth’s upper crust Jean-Pierre Gratier, Dag Dysthe, Francois Renard To cite this version: Jean-Pierre Gratier, Dag Dysthe, Francois Renard. The role of pressure solution creep in the ductility of the earth’s upper crust. Advances in Geophysics, Elsevier, 2013, 54, pp.47-179. 10.1016/B978-0- 12-380940-7.00002-0. insu-00799131 HAL Id: insu-00799131 https://hal-insu.archives-ouvertes.fr/insu-00799131 Submitted on 11 Mar 2013 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 1 The role of pressure solution creep in the ductility of the Earth’s upper crust Jean-Pierre Gratier1, Dag K. Dysthe2,3, and François Renard1,2 1Institut des Sciences de la Terre, Observatoire, CNRS, Université Joseph Fourier-Grenoble I, BP 53, 38041 Grenoble, France 2Physics of Geological Processes, University of Oslo, Norway 3Laboratoire Interdisciplinaire de Physique, BP 87, 38041 Grenoble, France The aim of this review is to characterize the role of pressure solution creep in the ductility of the Earth’s upper crust and to describe how this creep mechanism competes and interacts with other deformation mechanisms. -
How Hydration/Dehydration Reactions Accompany Key Earth and Life Processes
American Mineralogist, Volume 105, pages 1152–1160, 2020 Let there be water: How hydration/dehydration reactions accompany key Earth and life processes Alberto Vitale Brovarone1,2,*,§, Christopher J. Butch3, Alessandra Ciappa4, Henderson J. Cleaves II5,6,7, Agnès Elmaleh2, Manuele Faccenda8, Maureen Feineman9, Jörg Hermann10, Fabrizio Nestola8,†, Angelina Cordone11, and Donato Giovannelli4,5,11,12,13,‡ 1Dipartimento di Scienze della Terra, Università degli Studi di Torino, 10125 Torino, Italy 2Sorbonne Université, Muséum National d’Histoire Naturelle, UMR CNRS 7590, IRD, Institut de Minéralogie, de Physique des Matériaux et de Cosmochimie, IMPMC, 75005 Paris, France 3Department of Biomedical Engineering, Nanjing University, Nanjing, China 4Nano-Tech SpA, via d’Ancona 73/A, 60127 Osimo, Italy 5Earth-Life Science Institute, Tokyo Institute of Technology, 2-12-1-IE-1 Ookayama, Meguro-ku, Tokyo 152-8550, Japan 6Blue Marble Space Institute for Science, 1001 4th Avenue, Suite 3201, Seattle, Washington 98154, U.S.A. 7Institute for Advanced Study, 1 Einstein Drive, Princeton, New Jersey 08540, U.S.A. 8Dipartimento di Geoscienze, Università di Padova, 35131 Padova, Italy 9Department of Geosciences, Penn State 508 Deike Building, University Park, Pennsylvania 16802, U.S.A. 10Institute of Geological Sciences, University of Bern, 3012 Bern, Switzerland 11Department of Biology, University of Naples “Federico II”, via Cinthia, 80126, Naples, Italy 12Department of Marine and Coastal Science, Rutgers University, 71 Dudley Road, 08901 New Brunswick, New Jersey, U.S.A. 13Institute of Marine Biological and Biotechnological Resources, National Research Council of Italy, CNR-IRBIM, l.go Fiera della Pesca, 60121, Ancona, Italy Abstract Water plays a key role in shaping our planet and making life possible.