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Sediment accumulation and mixing in the Penobscot River and estuary, Maine.
Yeager, K M; Schwehr, K A; Schindler, K J; Santschi, P H.
Affiliation
  • Yeager KM; Sedimentary and Environmental Radiochemistry Research Laboratory (SER(2)L), Department of Earth and Environmental Sciences, University of Kentucky, Lexington, KY 40506, United States. Electronic address: kevin.yeager@uky.edu.
  • Schwehr KA; Laboratory for Oceanographic and Environmental Research (LOER), Department of Marine Science, Texas A&M University at Galveston, Galveston, TX 77554, United States. Electronic address: schwehrk@tamug.edu.
  • Schindler KJ; Sedimentary and Environmental Radiochemistry Research Laboratory (SER(2)L), Department of Earth and Environmental Sciences, University of Kentucky, Lexington, KY 40506, United States.
  • Santschi PH; Laboratory for Oceanographic and Environmental Research (LOER), Department of Marine Science, Texas A&M University at Galveston, Galveston, TX 77554, United States. Electronic address: santschi@tamug.edu.
Sci Total Environ ; 635: 228-239, 2018 Sep 01.
Article in En | MEDLINE | ID: mdl-29674257
ABSTRACT
Mercury (Hg) was discharged in the late 1960s into the Penobscot River by the Holtra-Chem chlor-alkali production facility, which was in operation from 1967 to 2000. To assess the transport and distribution of total Hg, and recovery of the river and estuary system from Hg pollution, physical and radiochemical data were assembled from sediment cores collected from 58 of 72 coring stations sampled in 2009. These stations were located throughout the lower Penobscot River, and included four principal study regions, the Penobscot River (PBR), Mendall Marsh (MM), the Orland River (OR), and the Penobscot estuary (ES). To provide the geochronology required to evaluate sedimentary total Hg profiles, 58 of 72 sediment cores were dated using the atmospheric radionuclide tracers 137Cs, 210Pb, and 239,240Pu. Sediment cores were assessed for depths of mixing, and for the determination of sediment accumulation rates using both geochemical (total Hg) and radiochemical data. At most stations, evidence for significant vertical mixing, derived from profiles of 7Be (where possible) and porosity, was restricted to the upper ~1-3cm. Thus, historic profiles of both total Hg and radionuclides were only minimally distorted, allowing a reconstruction of their depositional history. The pulse input tracers 137Cs and 239,240Pu used to assess sediment accumulation rates agreed well, while the steady state tracer 210Pb exhibited weaker agreement, likely due to irregular lateral sediment inputs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Water Pollutants, Chemical / Estuaries / Geologic Sediments / Rivers / Mercury Country/Region as subject: America do norte Language: En Journal: Sci Total Environ Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Water Pollutants, Chemical / Estuaries / Geologic Sediments / Rivers / Mercury Country/Region as subject: America do norte Language: En Journal: Sci Total Environ Year: 2018 Document type: Article