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  • 1
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    PANGAEA
    In:  Supplement to: Schwertmann, U; Carlson, L; Murad, E (1987): Properties of iron oxides in two Finnish lakes in relation to the environment of their formation. Clays and Clay Minerals, 35(4), 297-304, https://doi.org/10.1346/CCMN.1987.0350407
    Publication Date: 2023-08-28
    Description: Fifteen iron oxide accumulations from the bottoms of two Finnish lakes ("lake ores") were found to contain as much as 50% Fe. Differential X-ray powder diffraction and selective dissolution by oxalate showed that the samples consisted of poorly crystallized goethite and ferrihydrite. The crust ores of one lake had higher ferrihydrite to goethite ratios than the nodular ores of the other lake. The higher ferrihydrite proportion was attributed to a higher rate of Fe2+ supply from the ground water and/or a higher rate of oxidation as a function of water depth and bottom-sediment permeability. Values of Al-for-Fe substitution of the goethites determined from unit-cell dimensions agreed with those obtained from chemical extraction if the unit-cell volume rather than the c dimension was used. In very small goethite crystals a slight expansion of the a unit-cell dimension is probaby compensated by a corresponding contraction of the c dimension, so that a contraction of the c dimension need not necessarily be caused by Al substitution. The goethites of the two lakes differed significantly in their Al-for-Fe substitutions and hence in their unit-cell sizes, OH-bending characteristics, dehydroxylation temperatures, dissolution kinetics, and Mössbauer parameters. The difference in Al substitution (0 vs. 7 mole %) is attributed to the Al-supplying power of the bottom sediments: the silty-clayey sediments in one lake appear to have supplied A1 during goethite formation, whereas the gravelly-sandy sediments in the other lake did not. The compositions of the goethites thus reflect their environments of formation.
    Keywords: NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 2
    Publication Date: 2023-08-28
    Keywords: Color description; Deposit type; Depth, bottom/max; Dredge; DRG; Elevation of event; Enojarvi_C; Event label; Finland; Latitude of event; Longitude of event; Munsell Color System, powdered samples; Murtojarvi_C; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Sample ID; Sediment type
    Type: Dataset
    Format: text/tab-separated-values, 75 data points
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  • 3
    Publication Date: 2023-08-28
    Keywords: AAS, dithionite-soluble fraction; AAS, oxalate-soluble fraction; Carbon, total; DEPTH, sediment/rock; Dredge; DRG; Elevation of event; Enojarvi_C; Event label; Finland; Iron, soluble; Latitude of event; Longitude of event; Manganese, soluble; Minerals; Murtojarvi_C; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Photometry, dithionite-soluble fraction; Photometry, oxalate-soluble fraction; Sample ID; Silicon; Wet chemistry; Wösthoff carmograph; X-ray diffraction (XRD)
    Type: Dataset
    Format: text/tab-separated-values, 120 data points
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    European journal of soil science 50 (1999), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Hardsetting of soil comprises two contrasting, unfavourable physical conditions at different water contents, namely extreme hardness when dry and complete slaking when wet. This behaviour was changed by adding small amounts of ferrihydrite and aluminium hydroxide to the soil. The aggregation and its stability in the wet state increased, whereas the tensile strength of the dry soils decreased. Both resulted mainly by making the fine particles less mobile by aggregation. In some cases adding large amounts of Al hydroxide caused a resuspension of soil particles by reversing the charge, resulting in instability when wet and high stability when dry. We postulate that aggregation results from the interaction between negatively charged siliceous surfaces and positively charged oxides. In addition we think that newly formed Si–O–Fe bonds play a role in binding particles together as a result of a positive relation between the amount of ferrihydrite added and the oxalate-soluble Si. We conclude that hardsetting resulting from weak structure is caused by lack of aggregating agents such as metal hydroxides.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    European journal of soil science 45 (1994), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Iron (hydr)oxides are active phosphate sorbents in soils and sediments, but no information exists on phosphate (P) sorption by natural hematites. In this study, we characterized the chemical, mineralogical and P-sorption properties of 14 hematite-rich natural materials of different origins. Phosphate sorption was described by a modified Freundlich equation including a time term. Phosphate sorbed at 1d at an equilibrium concentration of 1 mg P dm−3 ranged widely (0.2–1.7 μmol m−2). After 1 d, hematites showed a marked slow sorption. At 75 d, and an equilibrium concentration of 6mg P dm−3, the total amount of P sorbed ranged between 0.8 and 4.1 μmol mp−2. Phosphate-sorption capacity was influenced by the morphology of the coherently scattering domains: the shorter the domains in the crystallographic c relative to the a direction, the lower the P-sorption capacity. This has been observed by other authors in synthetic hematites and agrees with the idea that the prismatic faces, which have singly co-ordinated Fe-OH groups, are more active in P-sorption than other faces. The average P sorption capacity of hematites was similar to that of natural goethites (2.6 μmol P m−2) but, in contrast to these, variability among samples was high. In comparison with goethites, hematites show slower sorption and lower affinity for phosphate.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    European journal of soil science 45 (1994), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    European journal of soil science 49 (1998), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Terre Rosse and Rendzinas occur on limestones close together under the same climatic conditions. Their differences in iron oxide mineralogy are believed to be due to differences in the pedoclimate. We monitored the soil moisture tension and the soil temperature over nearly 3 years in Terra Rossa-Rendzina pairs on hard limestone and soft chalk in Israel. The Terre Rosse dried out more rapidly than the Rendzinas mainly because of their smaller water-holding capacity. In summer, average soil temperatures in the Rendzinas were significantly lower than in the Terre Rosse.Haematite dominates the red Terre Rosse and goethite the yellower Rendzinas. This difference appears to be related to the soil climate, specifically the moisture regime of the two soils, and supports the hypothesis that release of Fe and formation of ferrihydrite in Terre Rosse during the wet winter is followed by transformation to haematite during marked desiccation in the dry summer. By contrast, wetter soil conditions in the Rendzinas direct the formation of Fe oxides more towards goethite. either directly or by transformation of ferrihydrite via solution.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 232 (1971), S. 624-625 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Near to the surface of profiles of these soils the proportion of red coloration decreases during these changes and the proportion of yellowish-brown colouring increases. A yellowish-brown rim forms on red mottles (in soils formed in the so-called mottled zones of former laterites exposed by ...
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Solid State Ionics 26 (1988), S. 181 
    ISSN: 0167-2738
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Catena 14 (1987), S. 519-531 
    ISSN: 0341-8162
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Geography , Geosciences
    Type of Medium: Electronic Resource
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