Balancing the Ocean
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Purification and Characterization of Bromocresol Purple for Spectrophotometric Seawater Alkalinity Titrations
University of Montana ScholarWorks at University of Montana Undergraduate Theses and Professional Papers 2016 PURIFICATION AND CHARACTERIZATION OF BROMOCRESOL PURPLE FOR SPECTROPHOTOMETRIC SEAWATER ALKALINITY TITRATIONS Taymee A. Brandon The University Of Montana, [email protected] Follow this and additional works at: https://scholarworks.umt.edu/utpp Part of the Analytical Chemistry Commons, and the Environmental Chemistry Commons Let us know how access to this document benefits ou.y Recommended Citation Brandon, Taymee A., "PURIFICATION AND CHARACTERIZATION OF BROMOCRESOL PURPLE FOR SPECTROPHOTOMETRIC SEAWATER ALKALINITY TITRATIONS" (2016). Undergraduate Theses and Professional Papers. 97. https://scholarworks.umt.edu/utpp/97 This Thesis is brought to you for free and open access by ScholarWorks at University of Montana. It has been accepted for inclusion in Undergraduate Theses and Professional Papers by an authorized administrator of ScholarWorks at University of Montana. For more information, please contact [email protected]. PURIFICATION AND CHARACTERIZATION OF BROMOCRESOL PURPLE FOR SPECTROPHOTOMETRIC SEAWATER ALKALINITY TITRATIONS By TAYMEE ANN MARIE BRANDON Undergraduate Thesis presented in partial fulfillment of the requirements for the University Scholar distinction Davidson Honors College University of Montana Missoula, MT May 2016 Approved by: Dr. Michael DeGrandpre Department of Chemistry and Biochemistry ABSTRACT Brandon, Taymee, B.S., May 2016 Chemistry Purification and Characterization of Bromocresol Purple for Spectrophotometric Seawater Alkalinity Titrations Faculty Mentor: Dr. Michael DeGrandpre The topic of my research is the purification of the sulfonephthalein indicator bromocresol purple (BCP). BCP is used as an acid-base indicator in seawater alkalinity determinations. Impurities in sulfonephthalein indicator salts often result in significant errors in pH values3. -
Geochemistry of Corals: Proxies of Past Ocean Chemistry, Ocean Circulation, and Climate
Proc. Natl. Acad. Sci. USA Vol. 94, pp. 8354–8361, August 1997 Colloquium Paper This paper was presented at a colloquium entitled ‘‘Carbon Dioxide and Climate Change,’’ organized by Charles D. Keeling, held November 13–15, 1995, at the National Academy of Sciences, Irvine, CA. Geochemistry of corals: Proxies of past ocean chemistry, ocean circulation, and climate ELLEN R. M. DRUFFEL Department of Earth System Science, University of California, Irvine, CA 92697 ABSTRACT This paper presents a discussion of the status Second, a synthesis is presented of the available proxy of the field of coral geochemistry as it relates to the recovery of records from corals as they relate to past climate, ocean past records of ocean chemistry, ocean circulation, and climate. circulation changes, and anthropogenic input of excess CO2. The first part is a brief review of coral biology, density banding, For some databases, the anthropogenic CO2 appears clear and and other important factors involved in understanding corals as globally distributed. For other databases it appears that vari- proxies of environmental variables. The second part is a syn- ability on interannual to decadal time scales complicates a thesis of the information available to date on extracting records straightforward attempt to separate natural perturbations of the carbon cycle and climate change. It is clear from these from the anthropogenic CO2 signal on the Earth’s environ- proxy records that decade time-scale variability of mixing pro- ment. Shen (4) presents a review of the types of coral archives cesses in the oceans is a dominant signal. That Western and available from the perspective of historical El Nin˜o-Southern Eastern tropical Pacific El Nin˜o-Southern Oscillation (ENSO) Oscillation (ENSO) influences on the tropical Pacific Ocean. -
Ocean Acidification in the Geological Past
UK Ocean Acidification programme synopsis Ocean acidification in the geological past www.oceanacidification.org.uk Lessons from the past Global-scale ocean acidification is happening now, as a result of human activities adding CO2 to the atmosphere. But ocean acidity has increased previously in the Earth’s history, as a result of natural changes in atmospheric composition. Of particular interest are past releases of CO2 that have occurred relatively rapidly in geological terms, since they may provide natural analogues for the effects of current acidification on chemical processes and marine life. Calcifying organisms (that construct their shells out of calcium carbonate) provide an important research focus, since they are preserved in the fossil record and are also likely to be especially sensitive to changes in ocean chemistry. Most of the palaeo-oceanographic Specific aims of the consortium study were: work in UKOA was carried out by a consortium project Abrupt ocean l To produce new estimates of seawater acidity and atmospheric CO2 levels for acidification events and their effects the period 40-65 million years ago in the Earth’s past, led by Paul l To study the response of the carbon cycle during the onset of the Paleocene - Pearson at Cardiff University. Formal Eocene thermal maximum (PETM) using new data from Tanzania and elsewhere partners were at Southampton, and new computer models University College London and the l To compare the PETM with other known ocean acidification events in the Open University, with additional Earth’s past contributions by researchers at Bristol, l To quantify the biotic response to ocean acidification events both directly Oxford, Yale and elsewhere. -
The Physical and Chemical Characteristics of Marine Primary Open Access Organic Aerosol: a Review Biogeosciences Biogeosciences Discussions B
EGU Journal Logos (RGB) Open Access Open Access Open Access Advances in Annales Nonlinear Processes Geosciences Geophysicae in Geophysics Open Access Open Access Natural Hazards Natural Hazards and Earth System and Earth System Sciences Sciences Discussions Open Access Open Access Atmos. Chem. Phys., 13, 3979–3996, 2013 Atmospheric Atmospheric www.atmos-chem-phys.net/13/3979/2013/ doi:10.5194/acp-13-3979-2013 Chemistry Chemistry © Author(s) 2013. CC Attribution 3.0 License. and Physics and Physics Discussions Open Access Open Access Atmospheric Atmospheric Measurement Measurement Techniques Techniques Discussions Open Access The physical and chemical characteristics of marine primary Open Access organic aerosol: a review Biogeosciences Biogeosciences Discussions B. Gantt and N. Meskhidze Department of Marine, Earth, and Atmospheric Sciences, North Carolina State University, Raleigh, North Carolina, USA Open Access Open Access Correspondence to: N. Meskhidze ([email protected]) Climate Climate Received: 19 July 2012 – Published in Atmos. Chem. Phys. Discuss.: 23 August 2012 of the Past of the Past Revised: 5 March 2013 – Accepted: 24 March 2013 – Published: 18 April 2013 Discussions Open Access Open Access Abstract. Knowledge of the physical characteristics and 1 Introduction Earth System chemical composition of marine organic aerosols is needed Earth System for the quantification of their effects on solar radiation trans- Dynamics Dynamics fer and cloud processes. This review examines research per- One of the largest uncertainties of the aerosol-cloud sys- Discussions tinent to the chemical composition, size distribution, mixing tem is the background concentration of natural aerosols, es- state, emission mechanism, photochemical oxidation and cli- pecially over clean marine regions where cloud condensa- Open Access Open Access matic impact of marine primary organic aerosol (POA) asso- tion nuclei (CCN) concentrationGeoscientific ranges from less than 100 Geoscientific −3 ciated with sea-spray. -
Ocean Acidification Due to Increasing Atmospheric Carbon Dioxide
Ocean acidification due to increasing atmospheric carbon dioxide Policy document 12/05 June 2005 ISBN 0 85403 617 2 This report can be found at www.royalsoc.ac.uk ISBN 0 85403 617 2 © The Royal Society 2005 Requests to reproduce all or part of this document should be submitted to: Science Policy Section The Royal Society 6-9 Carlton House Terrace London SW1Y 5AG email [email protected] Copy edited and typeset by The Clyvedon Press Ltd, Cardiff, UK ii | June 2005 | The Royal Society Ocean acidification due to increasing atmospheric carbon dioxide Ocean acidification due to increasing atmospheric carbon dioxide Contents Page Summary vi 1 Introduction 1 1.1 Background to the report 1 1.2 The oceans and carbon dioxide: acidification 1 1.3 Acidification and the surface oceans 2 1.4 Ocean life and acidification 2 1.5 Interaction with the Earth systems 2 1.6 Adaptation to and mitigation of ocean acidification 2 1.7 Artificial deep ocean storage of carbon dioxide 3 1.8 Conduct of the study 3 2 Effects of atmospheric CO2 enhancement on ocean chemistry 5 2.1 Introduction 5 2.2 The impact of increasing CO2 on the chemistry of ocean waters 5 2.2.1 The oceans and the carbon cycle 5 2.2.2 The oceans and carbon dioxide 6 2.2.3 The oceans as a carbonate buffer 6 2.3 Natural variation in pH of the oceans 6 2.4 Factors affecting CO2 uptake by the oceans 7 2.5 How oceans have responded to changes in atmospheric CO2 in the past 7 2.6 Change in ocean chemistry due to increases in atmospheric CO2 from human activities 9 2.6.1 Change to the oceans -
Sieving Hydrogen Isotopes Through Two Dimensional Crystals
Sieving hydrogen isotopes through two dimensional crystals M. Lozada-Hidalgo1, S. Hu1, O. Marshall1, A. Mishchenko1, A. N. Grigorenko1, R. A. W. Dryfe2, B. Radha1, I. V. Grigorieva1, A. K. Geim1 1School of Physics & Astronomy and 2School of Chemistry, University of Manchester, Manchester M13 9PL, UK One-atom-thick crystals are impermeable to all atoms and molecules but hydrogen ions (thermal protons) penetrate relatively easily through them. We show that monolayers of graphene and boron nitride can be used to separate hydrogen isotopes. Employing electrical measurements and mass spectrometry, we found that deuterons permeate through these crystals much slower than protons, resulting in a large separation factor of ≈10 at room temperature. The isotope effect is attributed to a difference of ≈60 meV between zero-point energies of incident protons and deuterons, which translates into the equivalent difference in the activation barriers posed by two dimensional crystals. In addition to providing insight into the proton transport mechanism, the demonstrated approach offers a competitive and scalable way for hydrogen isotope enrichment. Unlike conventional membranes used for sieving atomic and molecular species, monolayers of graphene and hexagonal boron nitride (hBN) exhibit subatomic selectivity (1-5). They are permeable to thermal protons (5) – and, of course, electrons (6) – but in the absence of structural defects are completely impermeable to larger, atomic species (1-5,7-10). Proton transport through these two-dimensional (2D) crystals was shown to be a thermally activated process, and the found energy barriers E of ≈0.3 and 0.8 eV for monolayers of hBN and graphene, respectively, were attributed to different densities of their electron clouds that have to be pierced by incident protons (5). -
Analysis of Seawater a Guide for the Analytical and Environmental Chemist T.R
Analysis of Seawater A Guide for the Analytical and Environmental Chemist T.R. Crompton Analysis of Seawater A Guide for the Analytical and Environmental Chemist With 48 Figures and 45 Tables 123 T.R. Crompton Hill Cottage (Bwthyn Yr Allt) Anglesey, Gwynedd United Kingdom Library of Congress Control Number: 2005929412 ISBN-10 3-540-26762-X Springer Berlin Heidelberg New York ISBN-13 978-3-540-26762-1 Springer Berlin Heidelberg New York DOI 10.1007/b95901 This work is subject to copyright. All rights reserved, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilm or in any other way, and storage in data banks. Duplication of this publication or parts thereof is permitted only under the provisions of the German Copyright Law of September 9, 1965, in its current version, and permission for use must always be obtained from Springer. Violations are liable for prosecution under the German Copyright Law. Springer is a part of Springer Science+Business Media springer.com © Springer-Verlag Berlin Heidelberg 2006 Printed in Germany The use of general descriptive names, registered names, trademarks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. Product liability: The publishers cannot guarantee the accuracy of any information about dosage and application contained in this book. In every individual case the user must check such information by consulting the relevant literature. -
Kinetic Hydrogen/Deuterium Isotope Effects in Multiple Proton Transfer Reactions
Z. Phys. Chem. 218 (2004) 17–49 by Oldenbourg Wissenschaftsverlag, München Kinetic Hydrogen/Deuterium Isotope Effects in Multiple Proton Transfer Reactions By Hans-Heinrich Limbach 1 , ∗, Oliver Klein 1 , Juan Miguel Lopez Del Amo 2, and Jose Elguero 2 1 Institut für Chemie der Freien Universität Berlin, Takustrasse 3, D-14195 Berlin, Germany 2 Instituto de Qu´ımica Medica,´ CSIC, Juan de la Cierva 3, E-28006 Madrid, Spain Dedicated to Prof. Dr. Herbert Zimmermann on the occasion of his 75th birthday (Received May 20, 2003; accepted July 8, 2003) Multiple Proton Transfer / Kinetic Isotope Effects In this paper, a description of multiple kinetic isotope effects (MKIE) of degenerate double, triple and quadruple proton transfer reactions in terms of formal kinetics is developped. Both single and multiple barrier processes are considered, corresponding to so-called “concerted” and “stepwise” reaction pathways. Each step is characterized by a rate constant and the transfer of a given H isotopes or ensemble of H isotopes. The MKIE are expanded in terms of kinetic H/D isotope effects P contributed by single sites in which a proton is transferred in the rate limiting steps. By combination with a modified Bell tunneling model the formalism developed can be used in order to take into account tunneling effects of both concerted and stepwise multiple proton transfers at low temperatures. 1. Introduction Proton transfer constitutes a very complex process, consisting not only of the transfer of a proton but also of diffusion, transport of electrical charges, reori- entation and reorganisation of the solvent molecules, hydrogen bond breaking and forming processes. -
The Origin of Life in Alkaline Hydrothermal Vents
ASTROBIOLOGY Volume 16, Number 2, 2016 Review Article ª Mary Ann Liebert, Inc. DOI: 10.1089/ast.2015.1406 The Origin of Life in Alkaline Hydrothermal Vents Victor Sojo,1,2 Barry Herschy,1 Alexandra Whicher,1 Eloi Camprubı´,1 and Nick Lane1,2 Abstract Over the last 70 years, prebiotic chemists have been very successful in synthesizing the molecules of life, from amino acids to nucleotides. Yet there is strikingly little resemblance between much of this chemistry and the metabolic pathways of cells, in terms of substrates, catalysts, and synthetic pathways. In contrast, alkaline hydrothermal vents offer conditions similar to those harnessed by modern autotrophs, but there has been limited experimental evidence that such conditions could drive prebiotic chemistry. In the Hadean, in the absence of oxygen, alkaline vents are proposed to have acted as electrochemical flow reactors, in which alkaline fluids saturated in H2 mixed with relatively acidic ocean waters rich in CO2, through a labyrinth of interconnected micropores with thin inorganic walls containing catalytic Fe(Ni)S minerals. The difference in pH across these thin barriers produced natural proton gradients with equivalent magnitude and polarity to the proton-motive force required for carbon fixation in extant bacteria and archaea. How such gradients could have powered carbon reduction or energy flux before the advent of organic protocells with genes and proteins is unknown. Work over the last decade suggests several possible hypotheses that are currently being tested in laboratory experiments, field observations, and phylogenetic reconstructions of ancestral metabolism. We analyze the perplexing differences in carbon and energy metabolism in methanogenic archaea and acetogenic bacteria to propose a possible ancestral mechanism of CO2 reduction in alkaline hydrothermal vents. -
A Deductive Approach to Biogenesis! Rob Hengeveld* Vrije Universiteit, Amsterdam, the Netherlands
ry: C ist urr m en e t Hengeveld, Organic Chem Curr Res 2015, 4:1 h R C e c s i e DOI: 10.4172/2161-0401.1000135 n a a r Organic Chemistry c g r h O ISSN: 2161-0401 Current Research ResearchReview Article Article OpenOpen Access Access A Deductive Approach to Biogenesis! Rob Hengeveld* Vrije Universiteit, Amsterdam, The Netherlands Abstract This article reviews the main arguments on the nature of the early startup of life. It first puts the biogenetical processes into a physical and systems-theoretical perspective. Biogenesis in this case would not be about the construction of individual molecules according to a chemical approach, but about building up an energetically self- sustaining, dynamically organized chemical system from scratch. Initially, this system would have separated out from generally operating physicochemical processes, gradually becoming more independent of them. As a system, it had to build up its structure stepwise, each stage being more complex and stable than the previous one, without, however, changing its basic structure too much; as long as the structure of a system stays intact, it still operates in the same way even if chemical constituents change. This property of a system became especially useful when the systems, which had already evolved and operated for some 1.3 billion years, had to adapt to new environmental conditions at the time of the Great Oxygen Event, the GOE, and some 2.5 billion years ago. As energy processing systems, their constituent molecules carry the energy and can as such be replaced by other, more efficient ones as soon as the system require, or as soon as external chemical conditions change. -
Actual Symmetry of Symmetric Molecular Adducts in the Gas Phase, Solution and in the Solid State
S S symmetry Review Actual Symmetry of Symmetric Molecular Adducts in the Gas Phase, Solution and in the Solid State Ilya G. Shenderovich Institute of Organic Chemistry, University of Regensburg, Universitaetstrasse 31, 93053 Regensburg, Germany; [email protected] Abstract: This review discusses molecular adducts, whose composition allows a symmetric structure. Such adducts are popular model systems, as they are useful for analyzing the effect of structure on the property selected for study since they allow one to reduce the number of parameters. The main objectives of this discussion are to evaluate the influence of the surroundings on the symmetry of these adducts, steric hindrances within the adducts, competition between different noncovalent interactions responsible for stabilizing the adducts, and experimental methods that can be used to study the symmetry at different time scales. This review considers the following central binding units: hydrogen (proton), halogen (anion), metal (cation), water (hydrogen peroxide). Keywords: hydrogen bonding; noncovalent interactions; isotope effect; cooperativity; water; organ- ometallic complexes; NMR; DFT 1. Introduction If something is perfectly symmetric, it can be boring, but it cannot be wrong. If Citation: Shenderovich, I.G. Actual something is asymmetric, it has potential to be questioned. Note, for example, the symmetry Symmetry of Symmetric Molecular of time in physics [1,2]. Symmetry also plays an important role in chemistry. Whether Adducts in the Gas Phase, Solution it is stereochemistry [3], soft matter self-assembly [4,5], solids [6,7], or diffusion [8], the and in the Solid State. Symmetry 2021, dependence of the physical and chemical properties of a molecular system on its symmetry 13, 756. -
Arctic Ocean Acidification
Abstract Volume Arctic Ocean Acidification Bergen, Norway 6-8 May, 2013 Arctic Ocean Acidification Bergen, Norway 6-8 May, 2013 Abstract Volume Contents Preface ................................................................................................................................................................................................................................................... 7 Background .................................................................................................................................................................................................................................... 7 Session 1 Acidification in the Arctic Ocean – set the scene ...................................................................................... 8 Plankton community responses to ocean acidification: implications for food webs and biogeochemical cycling..................... 8 Ulf Riebesell The alpha and omega of ocean acidification – biological impacts on benthic organisms .................................................................... 8 Sam Dupont Policy and Ocean Acidification ........................................................................................................................................................................................ 9 Carol Turley Session 2 Chemistry .......................................................................................................................................................................................................