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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Soil use and management 20 (2004), S. 0 
    ISSN: 1475-2743
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract. Land application of organic wastes can result in the accumulation of available soil phosphorus (P) and in an increase risk of eutrophication of surface and shallow groundwaters. We conducted laboratory experiments to examine the effect of waste application on the concentration of dissolved reactive phosphorus (DRP) in 1:5 soil to 0.005 m CaCl2 suspensions. Ten organic wastes, of which eight were mature composts, were applied to a P-rich Calcaric Fluvisol at rates ranging from 0 to 10% of soil by weight, and the difference in DRP concentration between suspensions containing waste and the untreated control (ΔDRP) was measured over a period of 300 days. In half of the suspensions of each waste–soil combination, 80 mg P (as KH2PO4) kg−1 soil was applied at day 14. Values of ΔDRP were generally positive, but a significant number of negative values were also recorded for some wastes and application rates, particularly at later sampling times if inorganic P had been added. Regression analyses revealed that ΔDRP (i) increased with increasing soluble reactive P at all times and (ii) increased in the short term, but decreased in the long term with increasing water soluble organic carbon in the waste. The fact that ΔDRP was sometimes negative for some waste types suggests that application of organic waste to soil does not necessarily increase eutrophication risks caused by soil P losses.
    Type of Medium: Electronic Resource
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  • 2
    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.
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  • 3
    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: The plant availability of phosphate applied to calcareous soils is affected by precipitation and adsorption reactions, the relative significance of which is not well known. We used extended P-sorption curves obtained at phosphate addition rates up to 340 mmol P kg−1 soil to examine the relative contribution of precipitation and adsorption by 24 calcareous Spanish Vertisols and Inceptisols. Adsorption was dominant at 1 day and at small rates of addition (10–35 mmol P kg−1). With increasing clay and Fe and Al oxides contents of the soil, more phosphate was sorbed before the sorption curve bent upwards, as a result of Ca phosphate precipitation. Sorption curves showed a nearly vertical intermediate region, the length of which increased with time, suggesting that a Ca phosphate buffered the concentration of P in solution. The buffering concentration decreased with time, suggesting a progressive transformation of more to less soluble forms of Ca phosphate. A phase less soluble than octacalcium phosphate seemed to control the concentration of P in solution at 180 days in most soils. The apparent solubility of this phase decreased with increasing carbonate content in the soil. Precipitation of poorly soluble Ca phosphates apparently predominated up to a P addition dose ranging from about 30 mmol P kg−1 in some soils to more than 340 mmol P kg−1 in others. At larger doses, the way additional P was bound to the solid phase was different; phosphate was probably adsorbed, at least in part, to low-affinity sites on silicate clays and oxides.The proportion of sorbed phosphate that was isotopically exchangeable decreased with time, soil carbonate content and P addition dose for doses 〈100 mmol P kg−1. This is consistent with the idea that P in Ca phosphates is less isotopically exchangeable than P adsorbed on mineral surfaces. At larger additions of P, isotopic exchangeability was unrelated to the soil properties measured, probably because there was a variety of sorbed P forms influenced in turn by different soil components.
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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: The sound management of agricultural soils that are heavily loaded with phosphorus (P) involves minimizing the losses of P responsible for eutrophication of surface waters, while ensuring enough P for crops. This paper describes a simple model to examine the compatibility of these two objectives in acid sandy soils in a temperate humid climate. The model is based on several assumptions regarding reversible and irreversible P sorption by P-reactive soil compounds (mainly poorly crystalline Fe and Al oxides) and release of P to water (water-P test). Model inputs are amount of P leached, P uptake by crops, and contents of poorly crystalline Fe and Al oxides in soil. The model predicts that reducing the amount of leached P to what is environmentally acceptable (e.g. 0.44 kg P ha–1 year–1, equivalent to 1 kg P2O5 ha–1 year–1) results in the long run in available soil P test values below target concentrations for optimum crop growth. When the amount of leached P is set to a fixed value the model predicts that soils with large contents of Fe and Al oxides can maintain the initial soil P test values for longer periods than other soils. The content in available P decreases if fertilizer P is applied to the soil at a rate equal to P uptake by crops. These results stress the difficulties involved in trying to make agricultural and environmental needs compatible in acid sandy soils.
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Electrochimica Acta 31 (1986), S. 1605-1608 
    ISSN: 0013-4686
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Electroanalytical Chemistry 303 (1991), S. 45-53 
    ISSN: 0022-0728
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Electroanalytical Chemistry 270 (1989), S. 381-393 
    ISSN: 0022-0728
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Crystal Growth 131 (1993), S. 115-123 
    ISSN: 0022-0248
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Geoderma 58 (1993), S. 107-123 
    ISSN: 0016-7061
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0022-0728
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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