Deposition of artificial radionuclides in sediments of Loch Etive, Scotland

被引:10
作者
Al-Qasmi, Hamza [1 ]
Law, Gareth T. W. [1 ]
Fifield, L. Keith [2 ]
Howe, John A. [3 ]
Brand, Tim [3 ]
Cowie, Gregory L. [4 ]
Law, Kathleen A. [1 ]
Livens, Francis R. [1 ]
机构
[1] Univ Manchester, Sch Chem, Ctr Radiochem Res, Oxford Rd, Manchester M13 9PL, Lancs, England
[2] Australian Natl Univ, Res Sch Phys & Engn, Dept Nucl Phys, Canberra, ACT 0200, Australia
[3] Scottish Assoc Marine Sci, Oban PA37 1QA, Argyll, Scotland
[4] Univ Edinburgh, Sch Geosci, Kings Bldg, Edinburgh EH9 3FE, Midlothian, Scotland
关键词
Americium; Uranium; Plutonium; Cesium; Sellafield; NORTHEAST IRISH SEA; ACCELERATOR MASS-SPECTROMETRY; MARINE-SEDIMENTS; EARLY DIAGENESIS; SCOTTISH FJORD; PLUTONIUM; URANIUM; BASIN; REMOBILIZATION; GEOCHEMISTRY;
D O I
10.1016/j.jenvrad.2018.02.001
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The nuclear fuel reprocessing plants on the Sellafield site (UK) have released low-level effluents into the Irish Sea under authorisation since 1952. This has led to the labelling of nearby offshore sediments with a range of artificial radionuclides. In turn, these sediments act as a long-term secondary source of both soluble and particle associated radionuclides to coastal areas. These radionuclides are of interest both in assessing possible environmental impacts and as tracers for marine processes. Here we present results from a study of the geochemistry of natural (U-234,U- 238) and artificial (Cs-137, (241)AM, (238)pu, (239+240)pu, and U-236) radionuclides and their accumulation in sediments from Loch Etive, Scotland. The data are interpreted in the context of the historical radioactive discharges to the Irish Sea and biogeochemical processes in marine sediments. Loch Etive is divided into two basins; a lower, seaward basin where the sedimentation rate (similar to 0.6 cm/yr) is about twice that of the more isolated upper basin (similar to 0.3 cm/yr). These accumulation rates are consistent with the broad distribution of Cs-137 in the sediment profiles which can be related to the maximum Sellafield discharges of Cs-137 in the mid-1970s and suggest that Cs-137 was mainly transported in solution to Loch Etive during that period. Enrichments of Mn, Fe, and Mo in sediment and porewater from both Loch Etive basins result from contemporary biogeochemical redox processes. Enrichments of U-238 and U-234 in the lower basin may be a result of the cycling of natural U. By contrast, the Sellafield-derived artificial isotope U-236 does not seem to be affected by the redox-driven reactions in the lower basin. The Pu-238/Pu-239,Pu- 240 ratios suggest contributions from both historical Sellafield discharges and global fallout Pu. The uniform sediment distributions of Pu and Am, which do not reflect Sellafield historical discharges, suggest the existence of a homogenous secondary source. This could be the offshore 'mud patch' in the vicinity of Sellafield from which the supply of radionuclides reflects time-integrated Sellafield discharges. This source could also account for the continuing supply of Cs to Loch Etive, even after substantial reductions in discharge from the Sellafield site.
引用
收藏
页码:45 / 52
页数:8
相关论文
共 59 条
[1]   Origin of artificial radionuclides in soil and sediment from North Wales [J].
Al-Qasmi, Hamza ;
Law, Gareth T. W. ;
Fifield, L. Keith ;
Livens, Francis R. .
JOURNAL OF ENVIRONMENTAL RADIOACTIVITY, 2016, 151 :244-249
[2]   URANIUM REMOVAL IN OCEANIC SEDIMENTS AND THE OCEANIC-U BALANCE [J].
BARNES, CE ;
COCHRAN, JK .
EARTH AND PLANETARY SCIENCE LETTERS, 1990, 97 (1-2) :94-101
[3]   WINDSCALE RADIOCESIUM IN THE CLYDE SEA AREA [J].
BAXTER, MS ;
MCKINLEY, IG ;
MACKENZIE, AB ;
JACK, W .
MARINE POLLUTION BULLETIN, 1979, 10 (04) :116-120
[4]   Plutonium(IV) reduction by the metal-reducing bacteria Geobacter metallireducens GS15 and Shewanella oneidensis MR1 [J].
Boukhalfa, Hakim ;
Icopini, Gary A. ;
Reilly, Sean D. ;
Neu, Mary P. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (18) :5897-5903
[5]   Microbial effects on mineral-radionuclide interactions and radionuclide solid-phase capture processes [J].
Brookshaw, D. R. ;
Pattrick, R. A. D. ;
Lloyd, J. R. ;
Vaughan, D. J. .
MINERALOGICAL MAGAZINE, 2012, 76 (03) :777-806
[6]   The vertical distribution of radionuclides in a Ribble Estuary saltmarsh: transport and deposition of radionuclides [J].
Brown, JE ;
McDonald, P ;
Parker, A ;
Rae, JE .
JOURNAL OF ENVIRONMENTAL RADIOACTIVITY, 1999, 43 (03) :259-275
[7]   Biogeochemical aspects of uranium mineralization, mining, milling, and remediation [J].
Campbell, Kate M. ;
Gallegos, Tanya J. ;
Landa, Edward R. .
APPLIED GEOCHEMISTRY, 2015, 57 :206-235
[8]  
Camplin W.C., 1986, RADIOACTIVITY SURFAC
[9]   The distribution of Mo, U, and Cd in relation to major redox species in muddy sediments of the Bay of Biscay [J].
Chaillou, G ;
Anschutz, P ;
Lavaux, G ;
Schäfer, J ;
Blanc, G .
MARINE CHEMISTRY, 2002, 80 (01) :41-59
[10]   THE GEOCHEMISTRY OF URANIUM AND THORIUM IN COASTAL MARINE-SEDIMENTS AND SEDIMENT PORE WATERS [J].
COCHRAN, JK ;
CAREY, AE ;
SHOLKOVITZ, ER ;
SURPRENANT, LD .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1986, 50 (05) :663-680