Particle transport of 234U-238U in the Kalix River and in the Baltic Sea

被引:97
作者
Andersson, PS
Porcelli, D
Wasserburg, GJ
Ingri, J
机构
[1] Swedish Museum Nat Hist, Lab Isotope Geol, S-10405 Stockholm, Sweden
[2] CALTECH, Div Geol & Planetary Sci, Charles Arms Lab, Lunat Asylum, Pasadena, CA 91125 USA
[3] Lulea Univ Technol, Div Appl Geol, S-97187 Lulea, Sweden
关键词
D O I
10.1016/S0016-7037(97)00342-6
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
The role of particles for U isotope transport was investigated in the Kalix River watershed, a particle-poor, Fe/Mn-rich river in northern Sweden, and in the Baltic Sea estuary. Particles >0.45 mu m are strongly enriched in U and contain 20-50% of the total riverine uranium budget and <1% of the total U in brackish waters (3-7 PSU). The particles have high delta(234)U which is close to that of dissolved U in the associated water, indicating that U on particles is dominantly nondetrital and isotopically exchanges rapidly with the ambient dissolved U. Particles at the river mouth are dominated by nondetrital Fe-Mn oxyhydroxides. Uranium and Fe are strongly correlated, clearly demonstrating that secondary Fe-oxyhydroxide is the major carrier of U in river water. There is no evidence for significant association of U with Mn-oxyhydroxide. Apparent U distribution coefficients (<(K)over cap (Fe)(d)>) were calculated for U between the authigenic Fe on particles and the solution. These values appear to be relatively constant throughout the year. This suggests an equilibrium between Fe in solution and authigenic Fe-oxyhydroxides on detrital particles. High values of <(K)over cap (Fe)(d)> calculated for one summer as well as high U concentrations in brackish waters can be explained by U scavenging by biogenic phases with low authigenic Fe content. Copyright (C) 1998 Elsevier Science Ltd.
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页码:385 / 392
页数:8
相关论文
共 30 条
[1]   SORPTION OF TRACE CONSTITUENTS FROM AQUEOUS-SOLUTIONS ONTO SECONDARY MINERALS .1. URANIUM [J].
AMES, LL ;
MCGARRAH, JE ;
WALKER, BA .
CLAYS AND CLAY MINERALS, 1983, 31 (05) :321-334
[2]   URANIUM AND RADIUM SORPTION ON AMORPHOUS FERRIC OXYHYDROXIDE [J].
AMES, LL ;
MCGARRAH, JE ;
WALKER, BA ;
SALTER, PF .
CHEMICAL GEOLOGY, 1983, 40 (1-2) :135-148
[3]   CONCENTRATION, VERTICAL FLUX, AND REMINERALIZATION OF PARTICULATE URANIUM IN SEA-WATER [J].
ANDERSON, RF .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1982, 46 (07) :1293-1299
[4]   STRONTIUM, DISSOLVED AND PARTICULATE LOADS IN FRESH AND BRACKISH WATERS - THE BALTIC SEA AND MISSISSIPPI DELTA [J].
ANDERSSON, PS ;
WASSERBURG, GJ ;
INGRI, J ;
STORDAL, MC .
EARTH AND PLANETARY SCIENCE LETTERS, 1994, 124 (1-4) :195-210
[5]   U-238-U-234 AND TH-232-TH-230 IN THE BALTIC SEA AND IN RIVER WATER [J].
ANDERSSON, PS ;
WASSERBURG, GJ ;
CHEN, JH ;
PAPANASTASSIOU, DA ;
INGRI, J .
EARTH AND PLANETARY SCIENCE LETTERS, 1995, 130 (1-4) :217-234
[6]   THE SOURCES AND TRANSPORT OF SR AND ND ISOTOPES IN THE BALTIC SEA [J].
ANDERSSON, PS ;
WASSERBURG, GJ ;
INGRI, J .
EARTH AND PLANETARY SCIENCE LETTERS, 1992, 113 (04) :459-472
[7]   DETRITAL BEDROCK ELEMENTS AS TRACERS OF SETTLING RESUSPENDED PARTICULATE MATTER IN A COASTAL AREA OF THE BALTIC SEA [J].
BLOMQVIST, S ;
LARSSON, U .
LIMNOLOGY AND OCEANOGRAPHY, 1994, 39 (04) :880-896
[8]   SELECTIVE REMOVAL OF TRACE-ELEMENTS FROM THE BALTIC BY SUSPENDED MATTER [J].
BOSTROM, K ;
BURMAN, JO ;
PONTER, C ;
INGRI, J .
MARINE CHEMISTRY, 1981, 10 (04) :335-354
[9]   EXPERIMENTAL-STUDY AND MODELING OF THE U(VI)-FE(OH)(3) SURFACE PRECIPITATION COPRECIPITATION EQUILIBRIA [J].
BRUNO, J ;
DEPABLO, J ;
DURO, L ;
FIGUEROLA, E .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1995, 59 (20) :4113-4123
[10]   U-238,U-234 AND TH-232 IN SEAWATER [J].
CHEN, JH ;
EDWARDS, RL ;
WASSERBURG, GJ .
EARTH AND PLANETARY SCIENCE LETTERS, 1986, 80 (3-4) :241-251