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Trace metal speciation in sea and pore water of the Gotland Deep,Baltic Sea, 1994
Affiliation:1. Department of Mathematics, Zayed University, P.O. Box 144534, Abu Dhabi, United Arab Emirates;2. Department of Mathematics, Central Michigan University, Mount Pleasant, MI 48859, USA;1. Qingdao Institute of Marine Geology, Qingdao, China;2. Laboratory for Marine Mineral Resources, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China;3. China Key Laboratory of Submarine Geosciences and Technology, Ministry of Education, Department of Marine Geoscience, Ocean University of China, Qingdao, China
Abstract:Studies on the speciation (particulate, colloidal, anionic and cationic forms) of trace metals (Cd, Co, Cu, Fe, Mn, Mo, Ni, Pb, Zn) in the water column and in pore waters of the Gotland Deep following the 1993/94 salt-water inflows showed dramatic changes in the total “dissolved” metal concentrations and in the ratios between different metal species in the freshly re-oxygenated waters below 125 m. Changes in concentrations were greatest for those metals for which the solubility differs with the redox state (Fe, Mn, Co) but were also noted for those metals which form insoluble sulphides (Cd, Pb, Cu, Zn) and/or stable complexes with natural ligands (Cu). Pore water data from segmented surface muds (0–200 mm) indicated that significant redox and related metal speciation changes took place in the surface sediments only a few weeks after the inflow of the oxygenated sea water into the Gotland Deep.
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