03B Risk Assessment and Cycling of Natural Organochlorines

Total Page:16

File Type:pdf, Size:1020Kb

03B Risk Assessment and Cycling of Natural Organochlorines FOCS Focus on Chlorine Science Edition 2013 ISSUE 03B Risk assessment and the cycle of natural To investigate potential chlorination rates, conifer- Rapid and extensive natural chlorination & 36 ous forest soil from the organic horizon with Clin dechlorination of soil organic matter was amended, and over time the amounts of 36Cl subsequently present as chloride (Clin) and non- David Bastviken (Stockholm University, Sweden) extractable organic chlorine were monitored (Clorg; using water and 0.1M potassium nitrate as extract- Co-authors of the original paper: Frida Thomsen, Teresia ants). Three different experiments were per- Svensson, Susanne Karlsson, Per Sandén, George Shaw, formed. Miroslav Matucha and Gunilla Öberg. In the first, transformation of Cl over 133 days un- During recent decades, the extent to which soil der oxic conditions was studied. This experiment organic matter can be chlorinated by natural pro- 36 showed a rapid initial increase in Clorg and after cesses has been debated. The amounts of organi- 36 eight days, 23% of the added Clin had been trans- cally bound chlorine (Clorg) in soils are often as 36 36 36 formed into Clorg. The proportion of Cl as Clorg large as or greater than the quantities of inorganic remained at this level until day 20. After that, the chlorine (chloride; Clin). Such high levels of Clorg 36 fraction of Clorg started to decrease and reached a even in very remote areas imply that its presence plateau at 8% by day 133. The decline in 36Cl af- cannot be explained by anthropogenic emissions org 36 ter day 20 can only be explained by substantial alone. Here, the authors present evidence from Cl transformation of Cl to Cl . The long term abun- tracer experiments that natural transformation of org in dance of Clorg is controlled by several different pro- chlorine between Clin and Clorg in soils can be rapid cesses including chlorination and dechlorination. and extensive, with specific rates up to 10% of the standing stock transformed per day, and that chlo- In the third experiment, the chlorination potential rination relies primarily on microbial or enzymatic under oxic and anoxic conditions was studied. Re- processes. sults indicated much higher net rates of formation 36 of Clorg under oxic conditions than in the absence of oxygen. This indicates that the natural formation Dr David Bastviken is Assistant Professor at Stockholm University, Sweden. He received an MSc from Uppsala University, Sweden, in 1997 and a PhD from Linköping University, Sweden, in 2002. His postdoctorate in 2003-2004 was at the Institute of Ecosystems Studies, Millbrook New York. Dr Bastviken’s research covers biogeochemistry, ecology, and microbial ecology. His early research examined aquatic food web dynamics following invasion of exotic species. He has also studied aquatic carbon cycling. Recent research has focused on natural chlorine transformations in soil, and methods for high precision measurements of rapid chlorination and dechlorination in the complex soil matrix. Current research interests include chlorine biogeochemistry, natural chlorination and dechlorination of organic matter, carbon biogeochemistry, and trace gas biogeochemistry including methane dynamics. P 01 Focus on Chlorine Science ISSUE 03B Edition 2013 36 of Clorg is regulated by biotic processes requiring The biodegradability of organochlorine oxygen, or that dechlorination processes are sub- stantially greater under anoxic conditions resulting compounds in lower net chlorination rates. All experiments showed substantial transformation 36 36 of Clin to Clorg within days under oxic condi- James Field (University of Arizona, USA) tions. The first experiment also indicates rapid Key to the natural chlorine cycle is the biodegrada- dechlorination of organochlorines in soil. To esti- tion of organochlorine compounds, converting mate rates, the possibility of simultaneously occur- chlorine back to chloride. Microorganisms have ring chlorination and dechlorination has to be con- developed diverse strategies for degrading organo- sidered. The best estimates of initial specific chlo- chlorine compounds, from reductive dehalogena- rination and dechlorination rates were in similar tion to hydrolytic and oxygenolytic chloride re- ranges, but dechlorination rates were always lease. Biodegradation should be considered as a greater than chlor-ination rates. Combined with redox reaction in which an electron donor is oxi- the frequent observation that Cl exceeds Cl in org in dised at the expense of an electron acceptor. organic soils, this suggests that some of the Clorg formed is resistant to dechlorination and accumu- Lower chlorinated compounds serve as an electron lates in spite of high specific dechlorination rates. donor and carbon source by being oxidised if an Results indicate that a maximum of 10% of the adequate electron acceptor is present. Higher 36 Clorg formed during the experiment could have chlorinated compounds can serve as electron ac- been refractory and that the remainder (>90%) was ceptors by being reductively de-halogenated in the subjected to dechlorination. presence of electron-donating compounds in the halorespiration process. Chlorinated solvents can The specific rates estimated in the present study also be cometabolically biotransformed by acci- represent potential rates since our experimental dental reactions with enzymes and cofactors in- conditions were dissimilar to field conditions. volved in the de-gradation of other substrates. Ex- Hence, our estimated specific rates should be con- amples of cometabolism include oxidation of chlo- sidered with caution. However, even if specific rinated solvents by monooxygenases and reduction chlorination rates under field conditions are 10- of chlorinated solvents by commonly-occurring re- fold lower than the estimates in the present study, duced cofactors in anaerobes (vitamin B12). the whole Clin pool is turned over by transfor- mation to Clorg at least twice a year. Therefore, Some natural organochlorines have a large turno- even a conservative interpretation of our results ver in the biosphere, e.g. chloromethane, chloro- supports the conclusion that soil chlorine transfor- form and methylated derivatives of chlorophenol. mations are rapid and extensive. Chloromethane is a good carbon and energy source for aerobic bacteria (Hypho-microbium and Methylobacterium) which mineralise the compound - completely to CO2 and Cl . The doubling times of Dr James Field is a Full Professor at the Department of Chemical and Environmental Engi- neering, University of Arizona (UA), USA. He joined the UA faculty as associate professor in 2001. Prior to that, he was Assistant Professor in the Department of Environmental Technology and in the Division of Industrial Microbiology at Wageningen University, The Netherlands. Dr Field received a PhD from Wageningen University in 1989. He has published over 150 scientific articles in peer reviewed journals. Current research interests include the biodegradation of chlorinated solvents; biotransformation of perchlo- rate and arsenic compounds; and autotrophic denitrification. He has worked on the natural production of organochlorine compounds by wood and litter-degrading fungi. P 02 Edition 2 013 ISSUE 03B aerobic chloromethane-utilising bacteria range valid to assume that such compounds will persist from 5.7 to 7.7h. The anaerobe, Acetobacterium indefinitely in the environment. dehalogenans is known to ferment chloromethane - to acetate and Cl in the presence of CO2. Aerobic and anaerobic bacteria use methyltransferases as The biogeochemical cycle of chlorine the first step in chloromethane degradation. The only known biodegradation of chloroform is co- metabolic. Under aerobic conditions, chloroform is Gunilla Öberg (Linköping University, Sweden) co-oxidised by methane or ammonia oxidising bac- teria using monooxygenases. Phosgene is a transi- In the early 1990s, it was revealed that large ent intermediate of the co-oxidation reaction re- amounts of naturally produced Clorg are present in soil. Later studies showed that chlorine partici- sulting in the formation of CO2. Chloroform is also reductively dehalogenated via the intermediates pates in a complex biogeochemical cycle in which dichloromethane and chloromethane in anaerobic the terrestrial environment appears to be a key environments. component. Recent studies suggest that a large portion of the Clin that is deposited in terrestrial Numerous bacteria use chlorophenols as a carbon environments is transformed to Clorg in soil or and energy source under aerobic conditions. The vege¬tation. The majority appears to become most studied strains utilising pentachlorophenol chlorinated organic matter. The process is not un- belong to the genera Mycobacterium and Sphingo- derstood, but there is strong evidence that the monas. Extensive evidence shows that chlorophe- transformation is driven by biotic processes, alt- nols are mineralised by these bacteria. The dou- hough abiotic processes have also been shown to bling times of aerobic chlorophenol utilising bacte- exist. ria range from 2.3 to 19.8h. In temperate regions, the chlorinated organic mat- Two main strategies are used for the aerobic deg- ter is subsequently transported to deeper soil lay- radation of chlorophenols. Lower chlorinated phe- ers with the soil water. It precipitates and is even- nols are initially attacked by mono-oxygenases tually mineralised, leading to the release of Clin yielding chlorocatechols as the first intermediates. following the
Recommended publications
  • Redalyc.Chlorine in the Stratosphere
    Atmósfera ISSN: 0187-6236 [email protected] Universidad Nacional Autónoma de México México VON CLARMANN, T. Chlorine in the stratosphere Atmósfera, vol. 26, núm. 3, 2013, pp. 415-458 Universidad Nacional Autónoma de México Distrito Federal, México Available in: http://www.redalyc.org/articulo.oa?id=56527859010 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Atmósfera 26(3), 415-458 (2013) Chlorine in the stratosphere T. VON CLARMANN Karlsruhe Institute of Technology, IMK, POB 3640, 76021 Karlsruhe, Germany E-mail: [email protected] Received May 22, 2013; accepted June 21, 2013 RESUMEN Este artículo reseña varios aspectos de los compuestos clorados presentes en la estratosfera, que incluyen tanto su papel como agentes químicos como su función de trazadores de los procesos dinámicos. En la estratosfera, el cloro reactivo se libera a partir de los clorofluorocarbonos y otros gases orgánicos que contienen cloro. La mayor parte del cloro reactivo se convierte en compuestos inertes que almacenan cloro, como ClONO2 y HCl. La reactivación del cloro estratosférico ocurre principalmente por reacciones heterogéneas en vórtices polares invernales, en combinación con la luz solar. Los ciclos catalíticos de Cl, ClO, BrO, Cl2 O2 , ClO2 y otros compuestos como NO, NO2, OH y HO2 destruyen el oxígeno impar (ozono y oxígeno atómico) de la atmósfera. El ciclo del dímero de ClO es particularmente importante en la formación del agujero de ozono, mientras que en latitudes medias el HOCl tiene alguna relevancia.
    [Show full text]
  • Global Sources and Distribution of Atmospheric Methyl Chloride
    GLOBAL SOURCES AND DISTRIBUTION OF ATMOSPHERIC METHYL CHLORIDE A Dissertation Presented to The Academic Faculty By Yasuko Yoshida In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy in the School of Earth and Atmospheric Sciences Georgia Institute of Technology August 2006 Global Sources and Distribution of Atmospheric Methyl Chloride Approved by: Dr. Yuhang Wang, Advisor Dr. Armistead Russell School of Earth and Atmospheric School of Civil and Environmental Sciences Engineering Georgia Institute of Technology Georgia Institute of Technology Dr. Robert Dickinson Dr. David Tan School of Earth and Atmospheric School of Earth and Atmospheric Sciences Sciences Georgia Institute of Technology Georgia Institute of Technology Dr. Athanasios Nenes School of Earth and Atmospheric Date Approved: June 16, 2006 Sciences Georgia Institute of Technology To Ben and Ikuko ACKNOWLEDGEMENTS I would like to express my sincere appreciation to my faculty advisor, Dr. Yuhang Wang, for his direction, guidance and support throughout my PhD study. I would also like to thank my thesis committee members, Dr. Robert Dickinson, Dr. Athanasios Nenes, Dr. Armistead Russell, and Dr. David Tan, for their assistance. I thank Dr. David Erickson and Dr. Jose L. Hernandez for providing the UWM- COADS data and helpful comments. I also thank Dr. Donald Blake for his suggestions. Special thanks go to Dr. Derek Cunnold for providing us the AGAGE data. I am grateful to CMDL and Dr. Geoff Dutton for providing us their unpublished data. I am also indebted to Dr. Daniel Jacob and Dr. Colette Heald for their help. I would like to thank Dr. Louis Giglio for his helpful suggestions.
    [Show full text]
  • Anthropogenic Cycles of the Elements: a Critical Review Wei-Qiang Chen* and T
    Critical Review pubs.acs.org/est Anthropogenic Cycles of the Elements: A Critical Review Wei-Qiang Chen* and T. E. Graedel Center for Industrial Ecology, School of Forestry and Environmental Studies, Yale University, New Haven, Connecticut 06511, United States *S Supporting Information ABSTRACT: A cycle is the quantitative characterization of the flows of a specific material into, within, and from a given system. An anthropogenic elemental cycle can be static (for a point in time) or dynamic (over a time interval). The about 350 publications collected for this review contain a total of 1074 individual cycle determinations, 989 static and 85 dynamic, for 59 elements; more than 90% of the publications have appeared since 2000. The cycles are of varying quality and completeness, with about 80% at country- or territory-level, addressing 45 elements, and 5% at global-level, addressing 30 elements. Despite their limitations, cycles have often been successful in revealing otherwise unknown information. Most of the elements for which no cycles exist are radioactively unstable or are used rarely and in small amounts. For a variety of reasons, the anthropogenic cycles of only perhaps a dozen elements are well characterized. For all the others, with cycles limited or nonexistent, our knowledge of types of uses, lifetimes in those uses, international trade, losses to the environment, and rates of recycling is quite limited, thereby making attempts to evaluate resource sustainability particularly problematic. 1. INTRODUCTION Thus, we exclude those biogeochemical cycles directed largely fl 2 As is now well-known, the human combustion of fossil fuels or completely at natural stocks and ows, as well as those that and the clearing of forest lands inject carbon dioxide into the are said to be anthropogenic cycles but actually only treat exchanges between the anthroposphere and the natural atmosphere.
    [Show full text]
  • Chlorine Cycling and the Fate of Cl in Terrestrial Environments
    Environmental Science and Pollution Research (2021) 28:7691–7709 https://doi.org/10.1007/s11356-020-12144-6 REVIEW ARTICLE Chlorine cycling and the fate of Cl in terrestrial environments Teresia Svensson1 & Henrik Kylin1,2 & Malin Montelius3 & Per Sandén1 & David Bastviken1 Received: 14 July 2020 /Accepted: 16 December 2020 / Published online: 5 January 2021 # The Author(s) 2021 Abstract Chlorine (Cl) in the terrestrial environment is of interest from multiple perspectives, including the use of chloride as a tracer for water flow and contaminant transport, organochlorine pollutants, Cl cycling, radioactive waste (radioecology; 36Cl is of large concern) and plant science (Cl as essential element for living plants). During the past decades, there has been a rapid development towards improved understanding of the terrestrial Cl cycle. There is a ubiquitous and extensive natural chlorination of organic matter in terrestrial ecosystems where naturally formed chlorinated organic compounds (Clorg) in soil frequently exceed the abundance of chloride. Chloride dominates import and export from terrestrial ecosystems while soil Clorg and biomass Cl can dominate the standing stock Cl. This has important implications for Cl transport, as chloride will enter the Cl pools resulting in prolonged residence times. Clearly, these pools must be considered separately in future monitoring programs addressing Cl cycling. Moreover, there are indications that (1) large amounts of Cl can accumulate in biomass, in some cases representing the main Cl pool; (2) emissions of volatile organic chlorines could be a significant export pathway of Cl and (3) that there is a production of Clorg in tissues of, e.g. plants and animals and that Cl can accumulate as, e.g.
    [Show full text]
  • Biological Chlorine Cycling in the Arctic Coastal Plain
    Biological chlorine cycling in the Arctic Coastal Plain Jaime E. Zlamal, Theodore K. Raab, Mark Little, Robert A. Edwards & David A. Lipson Biogeochemistry An International Journal ISSN 0168-2563 Biogeochemistry DOI 10.1007/s10533-017-0359-0 1 23 Your article is protected by copyright and all rights are held exclusively by Springer International Publishing AG. This e-offprint is for personal use only and shall not be self- archived in electronic repositories. If you wish to self-archive your article, please use the accepted manuscript version for posting on your own website. You may further deposit the accepted manuscript version in any repository, provided it is only made publicly available 12 months after official publication or later and provided acknowledgement is given to the original source of publication and a link is inserted to the published article on Springer's website. The link must be accompanied by the following text: "The final publication is available at link.springer.com”. 1 23 Author's personal copy Biogeochemistry DOI 10.1007/s10533-017-0359-0 Biological chlorine cycling in the Arctic Coastal Plain Jaime E. Zlamal . Theodore K. Raab . Mark Little . Robert A. Edwards . David A. Lipson Received: 1 April 2017 / Accepted: 30 July 2017 Ó Springer International Publishing AG 2017 Abstract This study explores biological chlorine compounds (Clorg) were correlated with organic matter cycling in coastal Arctic wet tundra soils. While many content, with a steeper slope in older soils. The previous chlorine-cycling studies have focused on concentration and chemical diversity of Clorg increased contaminated environments, it is now recognized that with soil development, with Clorg in younger soils more chlorine can cycle naturally between inorganic and closely resembling that of vegetation, and older soils organic forms in soils.
    [Show full text]
  • Chlorine in the Stratosphere
    Atmósfera 26(3), 415-458 (2013) Chlorine in the stratosphere T. VON CLARMANN Karlsruhe Institute of Technology, IMK, POB 3640, 76021 Karlsruhe, Germany E-mail: [email protected] Received May 22, 2013; accepted June 21, 2013 RESUMEN Este artículo reseña varios aspectos de los compuestos clorados presentes en la estratosfera, que incluyen tanto su papel como agentes químicos como su función de trazadores de los procesos dinámicos. En la estratosfera, el cloro reactivo se libera a partir de los clorofluorocarbonos y otros gases orgánicos que contienen cloro. La mayor parte del cloro reactivo se convierte en compuestos inertes que almacenan cloro, como ClONO2 y HCl. La reactivación del cloro estratosférico ocurre principalmente por reacciones heterogéneas en vórtices polares invernales, en combinación con la luz solar. Los ciclos catalíticos de Cl, ClO, BrO, Cl2 O2 , ClO2 y otros compuestos como NO, NO2, OH y HO2 destruyen el oxígeno impar (ozono y oxígeno atómico) de la atmósfera. El ciclo del dímero de ClO es particularmente importante en la formación del agujero de ozono, mientras que en latitudes medias el HOCl tiene alguna relevancia. También los eventos de protones solares pueden alterar la química del cloro estratosférico, aunque su efecto de activación o desactivación depende de las condiciones de iluminación. La vida media atmosférica de los clorofluorocarbonos determina la disponibilidad de las sustancias que destruyen el ozono en la estratosfera y depende de la circulación de Brewer-Dobson, que a su vez establece a qué altitudes y por cuánto tiempo está expuesta una porción de aire a la fotoquímica. Por su parte, los gases orgánicos clorados pueden usarse como trazadores para estimar la edad del aire estratosférico y así examinar la circulación de Brewer-Dobson.
    [Show full text]
  • Chlorine in the Stratosphere
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Atmósfera 26(3), 415-458 (2013) Chlorine in the stratosphere T. VON CLARMANN Karlsruhe Institute of Technology, IMK, POB 3640, 76021 Karlsruhe, Germany E-mail: [email protected] Received May 22, 2013; accepted June 21, 2013 RESUMEN Este artículo reseña varios aspectos de los compuestos clorados presentes en la estratosfera, que incluyen tanto su papel como agentes químicos como su función de trazadores de los procesos dinámicos. En la estratosfera, HOFORURUHDFWLYRVHOLEHUDDSDUWLUGHORVFORURÀXRURFDUERQRV\RWURVJDVHVRUJiQLFRVTXHFRQWLHQHQFORUR/D mayor parte del cloro reactivo se convierte en compuestos inertes que almacenan cloro, como ClONO2 y HCl. La reactivación del cloro estratosférico ocurre principalmente por reacciones heterogéneas en vórtices polares invernales, en combinación con la luz solar. Los ciclos catalíticos de Cl, ClO, BrO, Cl2 O2, ClO2 y otros compuestos como NO, NO2, OH y HO2 destruyen el oxígeno impar (ozono y oxígeno atómico) de la atmósfera. El ciclo del dímero de ClO es particularmente importante en la formación del agujero de ozono, mientras que en latitudes medias el HOCl tiene alguna relevancia. También los eventos de protones solares pueden alterar la química del cloro estratosférico, aunque su efecto de activación o desactivación depende GHODVFRQGLFLRQHVGHLOXPLQDFLyQ/DYLGDPHGLDDWPRVIpULFDGHORVFORURÀXRURFDUERQRVGHWHUPLQDOD disponibilidad de las sustancias que destruyen el ozono en la estratosfera y depende de la circulación de Brewer-Dobson, que a su vez establece a qué altitudes y por cuánto tiempo está expuesta una porción de aire a la fotoquímica. Por su parte, los gases orgánicos clorados pueden usarse como trazadores para estimar la edad del aire estratosférico y así examinar la circulación de Brewer-Dobson.
    [Show full text]
  • Ozone Depletion, Chlorine Activation and Water Vapor Observed in Spitsbergen
    Ozone depletion, chlorine activation and water vapor observed in Spitsbergen Dissertation zur Erlangung des Grades Dr. rer. nat. der Universitat¨ Bremen vorgelegt von Ingo Wohltmann April 2002 Berichte aus dem Institut fur¨ Umweltphysik – Band 0 herausgegeben von: Dr. Georg Heygster Universitat¨ Bremen, FB 1, Institut fur¨ Umweltphysik, Postfach 33 04 40, D-28334 Bremen URL http://www.iup.physik.uni-bremen.de E-Mail [email protected] Prufer:¨ Prof. Dr. Klaus Kunzi,¨ Prof. Dr. John Burrows c 2001 Ingo Wohltmann Contents 1 Physics and Chemistry of the Atmosphere 13 1.1 Composition of the Atmosphere . 13 1.2 Physics of the Atmosphere . 15 1.3 Dynamics of the Stratosphere . 18 1.4 Ozone Chemistry . 21 1.5 Ozone Distribution . 29 1.6 Chlorine Monoxide and Water Vapor . 31 1.7 Literature . 31 2 Instrument 33 2.1 Overview . 33 2.2 Radiative Transfer . 34 2.3 Absorption Coefficients . 36 2.4 Instrument Description . 40 2.4.1 Quasi Optics . 40 2.4.2 Antenna and Mixer . 42 2.4.3 Intermediate Frequency Chain . 44 2.4.4 Acousto Optical Spectrometer . 45 2.4.5 Bremen Radiometer . 45 2.5 Measurement Principle . 45 2.5.1 Totalpower Method . 46 2.5.2 Reference Beam Method . 47 3 Retrieval 49 3.1 Overview . 49 3.2 Optimal Estimation . 49 3.2.1 Resolution . 51 3.2.2 Errors . 53 3.2.3 Nonlinearities . 54 3.3 Retrieval . 55 3 3.3.1 General Features . 55 3.3.2 Forward Model Features . 59 3.3.3 Moist Weather Conditions . 72 3.4 Water Vapor, Spitsbergen .
    [Show full text]
  • Thermal Management of the Copper-Chlorine Cycle For
    THERMAL MANAGEMENT OF THE COPPER-CHLORINE CYCLE FOR HYDROGEN PRODUCTION: ANALYTICAL AND EXPERIMENTAL INVESTIGATION OF HEAT RECOVERY FROM MOLTEN SALT by Samane Ghandehariun A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY in The Faculty of Engineering and Applied Science Mechanical Engineering Program University of Ontario Institute of Technology August 2012 © Samane Ghandehariun, 2012 In the Name of God Most Gracious Most Merciful Abstract Hydrogen is known as a clean energy carrier which has the potential to play a major role in addressing the climate change and global warming, and thermochemical water splitting via the copper-chlorine cycle is a promising method of hydrogen production. In this research, thermal management of the copper-chlorine cycle for hydrogen production is investigated by performing analytical and experimental analyses of selected heat recovery options. First, the heat requirement of the copper-chlorine cycle is estimated. The pinch analysis is used to determine the maximum recoverable heat within the cycle, and where in the cycle the recovered heat can be used efficiently. It is shown that a major part of the potential heat recovery can be achieved by cooling and solidifying molten copper(I) chloride exiting one step in the cycle: the oxygen reactor. Heat transfer from molten CuCl can be carried out through direct contact or indirect contact methods. Predictive analytical models are developed to analyze a direct contact heat recovery process (i.e. a spray column) and an indirect contact heat recovery process (i.e. a double-pipe heat exchanger). Characteristics of a spray column, in which recovered heat from molten CuCl is used to produce superheated steam, are presented.
    [Show full text]
  • Trends of Stratospheric Chlorine and Fluorine Reservoir Species
    Trends of stratospheric chlorine and fluorine reservoir species Zur Erlangung des akademischen Grades eines DOKTORS DER NATURWISSENSCHAFTEN von der Fakultät für Physik des Karlsruher Instituts für Technologie genehmigte DISSERTATION von Dipl.-Met. Regina Kohlhepp aus Wolfratshausen Tag der mündlichen Prüfung: 6. Juli 2012 Referent: Prof. Dr. Herbert Fischer Korreferent: PD Dr. Michael Höpfner Abstract In the present thesis, ground-based measurements with Fourier transform infrared (FTIR) spectrome- ters are evaluated and compared with calculations by atmospheric models of different architecture. The species of primary interest are the chlorine and fluorine reservoir gases hydrogen chloride (HCl), chlorine nitrate (ClONO2), and hydrogen fluoride (HF). Their source gases are mainly anthropogenic chlorofluo- rocarbons (CFCs), hydrochlorofluorocarbons (HCFCs), and halons, which are so-called ozone-depleting substances. Because of this property, their emission was restricted in the Montreal Protocol in 1987 and its amendments and adjustments, leading to a subsequent phase-out. As a result of these reductions in the source gas emissions, the stratospheric inorganic chlorine content decreases with time since the late 1990s. This decline is confirmed by the FTIR measurements of HCl and ClONO2 total column abun- dances reported in the present thesis, at nearly all of the 17 measurement sites taking part in this study and belonging to the Network for the Detection of Atmospheric Composition Change (NDACC). The calculations of five atmospheric chemistry models (i.e., the Bremen 2-D model, KASIMA, SLIMCAT, EMAC, and SOCOL) reproduce this decrease. The main reason for including HF in this comparison study of models and measurements is that this substance is an indicator of anthropogenic influences.
    [Show full text]
  • Inference from Polar Ice Cores Thomas S
    South Dakota State University Open PRAIRIE: Open Public Research Access Institutional Repository and Information Exchange Theses and Dissertations 2017 Investigating the Atmospheric Production of Perchlorate: Inference from Polar Ice Cores Thomas S. Cox South Dakota State University Follow this and additional works at: http://openprairie.sdstate.edu/etd Part of the Analytical Chemistry Commons, Atmospheric Sciences Commons, and the Environmental Sciences Commons Recommended Citation Cox, Thomas S., "Investigating the Atmospheric Production of Perchlorate: Inference from Polar Ice Cores" (2017). Theses and Dissertations. 1664. http://openprairie.sdstate.edu/etd/1664 This Dissertation - Open Access is brought to you for free and open access by Open PRAIRIE: Open Public Research Access Institutional Repository and Information Exchange. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of Open PRAIRIE: Open Public Research Access Institutional Repository and Information Exchange. For more information, please contact [email protected]. INVESTIGATING THE ATMOSPHERIC PRODUCTION OF PERCHLORATE: INFERENCE FROM POLAR ICE CORES BY THOMAS S. COX A dissertation submitted in partial fulfillment of tHe requirements for tHe Doctor of Philosophy Major in CHemistry South Dakota State University 2017 iii ACKNOWLEDGEMENTS THere Have been many people wHo Have assisted in tHis project as well as assisted me on tHis academic endeavor, and I would like to take a moment to tHank these individuals. First and foremost, I would like to tHank my advisor, my mentor, my friend, Dr. Jihong Cole-Dai for His support, guidance, and Humor. At times, Dr. Cole-Dai has cHallenged me to my core, wHile also providing insight and clarity when needed.
    [Show full text]
  • Biogeochemical Cycles of Chlorine in the Coniferous Forest Ecosystem: Practical Implications
    Biogeochemical cycles of chlorine in the coniferous forest ecosystem: practical implications M. Matucha1, N. Clarke2, Z. Lachmanová3, S.T. Forczek1, K. Fuksová4, M. Gryndler5 1Institute of Experimental Botany, Academy of Sciences of the Czech Republic, Prague, Czech Republic 2Norwegian Forest and Landscape Institute, Aas, Norway 3Forestry and Game Management Research Institute, Prague, Czech Republic 4First Faculty of Medicine, Charles University, Prague, Czech Republic 5Institute of Microbiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic ABSTRACT Chlorine – one of the most widespread elements on the Earth – is present in the environment as chloride ion or bound to organic substances. The main source of chloride ions is the oceans while organically bound chlorine (OCl) comes from various sources, including anthropogenic ones. Chlorinated organic compounds were long considered to be only industrial products; nevertheless, organochlorines occur plentifully in natural ecosystems. However, re- cent investigations in temperate and boreal forest ecosystems have shown them to be products of biodegradation of soil organic matter under participation of chlorine. It is important to understand both the inorganic and organic biogeochemical cycling of chlorine in order to understand processes in the forest ecosystem and dangers as a result of human activities, i.e. emission and deposition of anthropogenic chlorinated compounds as well as those from natural processes. The minireview presented below provides a survey of contemporary knowledge of the state of the art and a basis for investigations of formation and degradation of organochlorines and monitoring of chloride and organochlorines in forest ecosystems, which has not been carried out in the Czech Republic yet. Keywords: chlorine cycle; chlorination; enzymatic; abiotic; organochlorines; adsorbable organic halogenes In nature, chlorine does not occur only as chlo- ated humic substances.
    [Show full text]