Speciation and Fate of Trace Metals in Estuarine Sediments Under Reduced and Oxidized Conditions, Seaplane Lagoon, Alameda Naval Air Station PDF Download
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Languages : en
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We have identified important chemical reactions that control the fate of metal-contaminated estuarine sediments if they are left undisturbed (in situ) or if they are dredged. We combined information on the molecular bonding of metals in solids from X-ray absorption spectroscopy (XAS) with thermodynamic and kinetic driving forces obtained from dissolved metal concentrations to deduce the dominant reactions under reduced and oxidized conditions. We evaluated the in situ geochemistry of metals (cadmium, chromium, iron, lead, manganese and zinc) as a function of sediment depth (to 100 cm) from a 60-year record of contamination at the Alameda Naval Air Station, California. Results from XAS and thermodynamic modeling of porewaters show that cadmium and most of the zinc form stable sulfide phases, and that lead and chromium are associated with stable carbonate, phosphate, phyllosilicate, or oxide minerals. Therefore, there is minimal risk associated with the release of these trace metals from the deeper sediments contaminated prior to the Clean Water Act (1975) as long as reducing conditions are maintained. Increased concentrations of dissolved metals with depth were indicative of the formation of metal HS- complexes. The sediments also contain zinc, chromium, and manganese associated with detrital iron-rich phyllosilicates and/or oxides. These phases are recalcitrant at near-neutral pH and do not undergo reductive dissolution within the 60-year depositional history of sediments at this site. The fate of these metals during dredging was evaluated by comparing in situ geochemistry with that of sediments oxidized by seawater in laboratory experiments. Cadmium and zinc pose the greatest hazard from dredging because their sulfides were highly reactive in seawater. However, their dissolved concentrations under oxic conditions were limited eventually by sorption to or co-precipitation with an iron (oxy)hydroxide. About 50% of the reacted CdS and 80% of the reacted ZnS were bonded to an oxide-substrate at the end of the 90-day oxidation experiment. Lead and chromium pose a minimal hazard from dredging because they are bonded to relatively insoluble carbonate, phosphate, phyllosilicate, or oxide minerals that are stable in seawater. These results point out the specific chemical behavior of individual metals in estuarine sediments, and the need for direct confirmation of metal speciation in order to constrain predictive models that realistically assess the fate of metals in urban harbors and coastal sediments.
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Languages : en
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We have identified important chemical reactions that control the fate of metal-contaminated estuarine sediments if they are left undisturbed (in situ) or if they are dredged. We combined information on the molecular bonding of metals in solids from X-ray absorption spectroscopy (XAS) with thermodynamic and kinetic driving forces obtained from dissolved metal concentrations to deduce the dominant reactions under reduced and oxidized conditions. We evaluated the in situ geochemistry of metals (cadmium, chromium, iron, lead, manganese and zinc) as a function of sediment depth (to 100 cm) from a 60-year record of contamination at the Alameda Naval Air Station, California. Results from XAS and thermodynamic modeling of porewaters show that cadmium and most of the zinc form stable sulfide phases, and that lead and chromium are associated with stable carbonate, phosphate, phyllosilicate, or oxide minerals. Therefore, there is minimal risk associated with the release of these trace metals from the deeper sediments contaminated prior to the Clean Water Act (1975) as long as reducing conditions are maintained. Increased concentrations of dissolved metals with depth were indicative of the formation of metal HS- complexes. The sediments also contain zinc, chromium, and manganese associated with detrital iron-rich phyllosilicates and/or oxides. These phases are recalcitrant at near-neutral pH and do not undergo reductive dissolution within the 60-year depositional history of sediments at this site. The fate of these metals during dredging was evaluated by comparing in situ geochemistry with that of sediments oxidized by seawater in laboratory experiments. Cadmium and zinc pose the greatest hazard from dredging because their sulfides were highly reactive in seawater. However, their dissolved concentrations under oxic conditions were limited eventually by sorption to or co-precipitation with an iron (oxy)hydroxide. About 50% of the reacted CdS and 80% of the reacted ZnS were bonded to an oxide-substrate at the end of the 90-day oxidation experiment. Lead and chromium pose a minimal hazard from dredging because they are bonded to relatively insoluble carbonate, phosphate, phyllosilicate, or oxide minerals that are stable in seawater. These results point out the specific chemical behavior of individual metals in estuarine sediments, and the need for direct confirmation of metal speciation in order to constrain predictive models that realistically assess the fate of metals in urban harbors and coastal sediments.
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Category : Arsenic
Languages : en
Pages : 124
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V.3 ... consists of individual chapters that describe 1) the conceptual background for radionuclides, including tritium, radon, strontium, technetium, uranium, iodine, radium, thorium, cesium, plutonium-americium and 2) data requirements to be met during site characterization.
Author: John William Moreau
Publisher:
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Languages : en
Pages : 528
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Author: Brandy Marie Toner
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Category :
Languages : en
Pages : 400
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Author: Camille Gaulier
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Languages : en
Pages : 0
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Estuarine and coastal ecosystems provide multiple ecological, social and economic services. They are a source of food, income and are at the heart of marine trade, merchant shipping and sea transport. They therefore play a key role in our modern world and their conservation from an environmental point of view is today critical. Despite all the efforts done in environmental management, pollution associated with the rapid coastal development and intensive industrialization was inevitable and still remains one of the main threats towards marine ecosystems today. Specifically, trace metal contamination is of specific concern as coastal areas are generally prone to accumulate them. Most trace metals exhibit a dual role in marine waters: they act as nutrients in low concentrations, yet rapidly have toxic effects in higher concentration ranges. Continuous monitoring of their concentrations in estuarine and coastal ecosystems is therefore needed to better understand their biogeochemical behavior in such marine environments. However, limited knowledge exists on their bioavailability towards marine organisms: especially as the toxicity of these metals is not only related to their concentration but also strongly linked with their speciation which shows both seasonal and spatial variations. Thus, the main objective of this PhD research was to investigate the biogeochemical cycles of various trace metals and unravel their speciation and bioavailability in various aquatic systems: from very dynamic mixing zones of the Scheldt estuary to coastal harbors and shallow seawaters of the North Sea, and even to deeper and anoxic regions of the Baltic Sea. Trace metal concentrations and speciation were explored seasonally and spatially along horizontal and vertical gradients, and a comparison of classic active samplings of dissolved trace metals with a passive sampling technique (Diffusive Gradients in Thin-films; DGT) was carried out. The DGT technique was successfully used for the in-situ measurement of labile metals and eventually constitutes a good surrogate to the biomonitoring of trace elements (e.g. use of mussels, algae, etc.). This method offsets the lack of knowledge in terms of water quality monitoring and the results challenge the classic criteria which are used by international regulatory requirements (e.g. WFD, MSFD) and local commitments (e.g. OSPAR, HELCOM). Indeed, new criteria based on labile metal species instead of total dissolved species should be considered in the future. Such approach of trace metal speciation and assessment in aquatic systems could surely lead to a more integrated environmental management and improve our knowledge on anthropogenic impacts and pollutant fluxes. Moreover, it is eventually the main key to explain and predict bioavailability and potential toxicity of trace metals to the marine fauna and flora. This work therefore invites you to dive into a journey along our coasts, from urbanized areas to wild open seas, from their surface to their deepest waters.
Author: HerbertE. Allen
Publisher: Routledge
ISBN: 1351432168
Category : Science
Languages : en
Pages : 320
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Over the past decade the sediments of many rivers, lakes, and estuaries have been contaminated by inorganic and organic materials. Contaminants from sediments, under certain conditions, can be released into overlying waters. Thus, sediments may be an important source of contaminants to waters in which littoral and atmospheric contaminants have been reduced or eliminated. Often found in aquatic sediments, metals are exposed to many reactions, such as sorption and precipitation, and are greatly influenced by the redox conditions in the sediment. The reactions - usually over a period of time - reflect biotic processing as well as chemical transformations. This book describes these important processes. Metal Contaminated Aquatic Sediments outlines advances in environmental chemistry, effective new modeling techniques, applications for biological treatment, and cycling and transport of trace metals in sedimentary environments. Each chapter contains a detailed reference section that draws upon a stunning array of sources. The book includes many figures and tables that illustrate the process under discussion. Features
Author: C. Wong
Publisher: Springer Science & Business Media
ISBN: 1475768648
Category : Science
Languages : en
Pages : 913
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In recent years, rapid scientific advances have been shattering classical concepts of oceanic trace metals concentrations. Most of the data gathered before the mid-1970s have had to be discarded. Possible associations of organic and inorganic ligands with the metals were throwing views of metal speciation into great uncertainty. Biological effects of metals need to be re-examined after recent revelations of unsuspected metal contaminations in methodology. The investigations appear chaotic, yet exciting. It implies that a new order is going to replace the past. Now, an opportunity opens its door to a brave new world for the young generation of scientists to put metal chemistries in the oceans into perspectiveo This N. AoToO. International Conference on "Trace Metals in Sea Water" hoped to catalyze this exciting process of unifying various aspects of trace metals in sea water in future years o The Conference, in the form of an Advanced Research Institute supported by the Scientific Affairs Division of NoAoT. O. supple mented by further assistance of the UoS. Office of Naval "Research, was held at the "Ettore Majorana" Center for Scientific Culture in the medieval town of Erice on the island of Sicily, Italy from March 30 to April 3, 1981. It was the first organized gathering of international scientists in this specialized field. Seventy scientists with various expertise in different aspects of the subject were present: including those from NoAoT. Oo countries (Canada, France, F. R. Germany, Greece, Iceland, Italy, U. K.
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Publisher: Nordic Council of Ministers
ISBN: 9789289303910
Category : Chemical oceanography
Languages : en
Pages : 72
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Languages : en
Pages : 6
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The long-term goals of our research have been to: 1) Continue to develop and evaluate highly sensitive analytical techniques for determining the concentrations of bioactive trace metals in seawater and the extent of their complexation or chelation by natural organic ligands. 2) Further our basic understanding of the role of chemical speciation with respect to both trace metal toxicity and bio-limitation of phytoplankton within coastal and estuarine environments for a suite of bioactive trace metals--Mn, Fe, Ni, Cu, Zn, Cd and Pb. This includes the influence of organic complexation on the reactivity of these trace metals, as well as gaining insight into the production and fate of the metal chelating organic ligands. This research has been particularly complementary to that of Bill Sunda, another Harbor Processes PI, by providing the field data needed to evaluate the applicability of his laboratory studies examining the effects of these trace metals.
Author: Matthew Paul Hurst
Publisher:
ISBN:
Category :
Languages : en
Pages : 414
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