| 1. |
- Andersson, K, et al.
(författare)
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Colloidal rare earth elements in a boreal river: Changing sources and distributions during the spring flood
- 2006
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Ingår i: Geochimica Et Cosmochimica Acta. - : Elsevier BV. - 0016-7037 .- 1872-9533. ; 70:13, s. 3261-3274
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Tidskriftsartikel (refereegranskat)abstract
- Variations in the physico-chemical speciation of the rare earth elements (REE) have been investigated in a subarctic boreal river during an intense spring flood event using prefiltered (< 100 mu m) samples, cross-flow (ultra)filtration (CFF), flow field-flow fractionation (FIFFF), and diffusive gradients in thin films (DGT). This combination of techniques has provided new information regarding the release and transport of the REE in river water. The colloidal material can be described in terms of two fractions dominated by carbon and iron, respectively. These two fractions, termed colloidal carrier phases, showed significant temporal changes in concentration and size distribution. Before the spring flood, colloidal carbon concentrations were low, the colloids being dominated by relatively large iron colloids. Colloidal concentrations increased sharply during the spring flood, with smaller carbon colloids dominating. Following the spring flood, colloidal concentrations decreased again, smaller carbon colloids still dominating. The REE are transported mainly in the particulate and colloidal phases. Before the spring flood, the REE composition of all measured fractions was similar to local till. During the spring flood, the REE concentrations in the colloidal and particulate fractions increased. The increase was most marked for the lighter REE, which therefore showed a strong enrichment when normalized to local till. Following the spring flood, the REE concentrations decreased again and reverted to a distribution similar to local till. These changes in the concentration and distributions of carbon iron and REE are interpreted in terms of changing hydrological flow paths in soil and bedrock which occur during the spring flood. (c) 2006 Elsevier Inc. All rights reserved.
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| 2. |
- Dahlqvist, Ralf, et al.
(författare)
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Temporal variations of colloidal carrier phases and associated trace elements in a boreal river
- 2007
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Ingår i: Geochimica et Cosmochimica Acta. - : Elsevier BV. - 0016-7037 .- 1872-9533. ; 71:22, s. 5339-5354
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Tidskriftsartikel (refereegranskat)abstract
- Elemental size distributions, from truly dissolved through colloidal to particulate, have been studied in a subarctic boreal river. The measurements, carried out during 2002, ranged from winter to summer conditions, including an intense spring flood event. Results are reported for a total of 42 elements. Size distributions were characterised using a combination of cross-flow (ultra)filtration (CFF), flow field-flow fractionation (FIFFF), and diffusive gradients in thin-films (DGT). The three techniques showed similar trends, but quantitative comparisons reveal some important differences that warrant further investigation. Previous work has identified two colloidal carrier phases in fresh waters, dominated by iron and carbon, respectively. The majority of the elements studied are associated with one or both of these colloidal carrier phases. The exceptions are the alkali metals and several anions that are only very weakly associated with colloidal material, and which therefore occur mainly as truly dissolved material (< 1 kDa in molecular weight). We discuss the likely origin for the two colloidal carrier phases and consider how associated trace elements fit into the geochemical framework. The relative affinities of the elements for iron and carbon colloidal carrier phases are related to their chemistries, and are compared with earlier data from the Delsjo Creek in southern Sweden. Elemental colloidal concentrations show strong seasonal variations related to changes in the colloidal carrier phase(s) with which they associate. In particular, many elements show a strong spring maximum in colloidal concentrations associated with the strong maximum in colloidal carbon concentration during the spring flood.
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| 3. |
- Ingri, Johan, et al.
(författare)
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Fractionation of iron isotopes during estuarine mixing in Ob, Yenisey and Lena freshwater plumes
- 2009
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Ingår i: Geochimica et Cosmochimica Acta. - 0016-7037 .- 1872-9533. ; 73:13, Suppl. S, s. A569-
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- Iron isotopes were measured in suspended matter (>0.2 µm) in the Ob, Yenisey and Lena River freshwater plumes during the International Siberian Shelf Study 2008 (ISSS-08). The δ56Fe value was around zero within the Lena River and close to the river mouth, but changed to more negative values in the outer parts of the plume. In both the Ob and Yenisey plumes suspended matter in the surface water had clearly negative values whereas samples close to the bottom showed values close to zero.It has previously been suggested that total Fe in river suspended matter (>0.2µm) in boreal regions is roughly a mixture of three phases, detrital particles (δ56Fe around zero), oxyhydroxide particles (δ56Fe positive) and C-Fe particles (δ56Fe negative). We suggest that the δ56Fe pattern observed in this study is the result of relatively rapid removal of detrital particles and Fe-oxyhydroxides, leaving a suspended fraction with negative values in the surface water in the outer parts of the freshwater plumes. Hence, during estuarine mixing of suspended particles heavy iron isotopes are deposited close to the river mouth, whereas light isotopes are exported to open ocean water.
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| 4. |
- Ingri, Johan, et al.
(författare)
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Iron isotope fractionation in river colloidal matter
- 2006
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Ingår i: Earth and Planetary Science Letters. - : Elsevier BV. - 0012-821X .- 1385-013X. ; 245:3-4, s. 792-798
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Tidskriftsartikel (refereegranskat)abstract
- Temporal variations in the iron isotopic composition, δ56Fe between − 0.13‰ and 0.31‰, have been measured in the suspended fraction in a Boreal river. The major mechanism behind these variations is temporal mixing between two types of particles–colloids, Fe-oxyhydroxides and Fe–C colloids. Data in this study indicate that these two types of colloids have different Fe-isotope composition. The Fe–C colloid has a negative δ56Fe value whereas the Fe-oxyhydroxide colloid is enriched in 56Fe. These two types of colloidal matter have different hydrogeochemical origin. The Fe–C colloid reaches the river during storm events when the upper sections of the soil profile (O and E horizons) are flooded by a rising water table. Colloidal Fe-oxyhydroxides reach the river via inflow and subsequent oxidation of groundwater enriched in dissolved Fe(II).
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