51 research outputs found

    Nickel speciation and ecotoxicity in European natural surface waters: development, refinement and validation of bioavailability models

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    The accurate prediction of Ni ecotoxicity in natural surface water with bioavailability models such as the biotic ligand model (BLM) depends on how well these models can predict both the speciation of Ni (i.e. Ni2+ concentration), the toxicity of Ni2+ ions to an organism, and the effects of water chemistry parameters thereupon, such as dissolved organic carbon (DOC), pH, and water hardness. The overall aim of the study was to calibrate existing speciation models to Ni speciation in natural surface waters and to use these data to validate and/or refine bioavailability models for aquatic organisms from three trophic levels, i.e. algae, invertebrates (daphnids), and fish. The developed chronic Ni toxicity models for daphnids, fish and algae exhibit sufficiently high predictive capacities to yield a marked reduction of uncertainty associated with differences in chronic Ni bioavailability among different test waters. This is due to the fact that they can predict both Ni2+ concentrations as a function of dissolved Ni and water chemistry (mainly DOC, pH, Ca, Mg), as well as the toxicity of the Ni2+ ion as a function of water chemistry (mainly pH, Ca, Mg). The use of the models presented in the present study for normalizing Ni toxicity data will therefore decrease the overall uncertainty of the risk assessment, provided that the variability of bioavailability modifying parameters across different EU regions and water bodies is acknowledged

    Effect of soil properties on time-dependent fixation (ageing) of selenate

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    © 2020 Elsevier B.V. Previous biofortification studies have established that the residual effect of added selenium (Se) fertilisers on second-season crops is minimal. To explore the fate of exogenous Se in soil, chemical and biological methods were employed to assess the change in Se bioavailability with time. Eight soils varying in physicochemical properties were spiked with sodium selenate (0.5 mg kg−1 Se) and incubated at 25 °C for different periods (1, 30, 60, 90 and 300 d). At the end of the incubation, soil Se was fractionated by a sequential extraction procedure into ‘soluble’, ‘adsorbed’ and ‘organically-bound’ Se fractions. Simultaneously, wheat was grown in the Se-aged soils, under controlled conditions for six weeks, and uptake was determined. A general decrease in Se solubility over time was observed, but the rate of decrease varied depending on soil type. A reversible first order model fitted the Se ageing kinetics well, except in an Oxisol. The most pronounced ageing was observed in calcareous soils. Concentrations of Se in the shoots of wheat grown in freshly spiked soils ranged from 71.8 ± 17.5 mg kg−1 in calcareous soils to 110 ± 31.6 mg kg−1 in non-calcareous, low-OM soils. With ageing, shoot Se concentrations decreased t

    Improving the efficacy of selenium fertilizers for wheat biofortification

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    © 2019, The Author(s). Increasing the selenium (Se) concentration of staple crops by fertilization is a valuable pathway to increase Se in the human diet, thus preventing Se deficiency. A pot trial was set up to investigate whether the application of 3.33 µg kg−1 of Se (equivalent to 10 g ha−1) to wheat can be made more efficient by its co-application with macronutrient carriers, either to the soil or to the leaves. In the soil, Se was applied either on its own (selenate only) or as a granular, Se-enriched macronutrient fertilizer supplying nitrogen, phosphorus, potassium or sulfur. Selenium was also applied to leaves at head emergence with, or without, 2% w/v N fertilizers. With grain Se concentrations varying from 0.13–0.84 mg kg−1, soil application of selenate-only was 2–15 times more effective than granular Se-enriched macronutrient fertilizers in raising grain Se concentrations. Co-application of foliar Se with an N carrier doubled the Se concentration in wheat grains compared to the application of foliar Se on its own, the majority of which was in the highly bioavailable selenomethionine fraction. Results from this study demonstrate the possibility of improving the efficacy of Se fertilizers, which could enrich crops with Se without additional application costs in the field

    Using 77Se-Labelled Foliar Fertilisers to Determine How Se Transfers Within Wheat Over Time

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    Foliar selenium (Se) fertilisation has been shown to be more efficient than soil-applied fertilisation, but the dynamics of absorption and translocation have not yet been explored. An experiment was undertaken to investigate time-dependent changes in the absorption, transformation, and distribution of Se in wheat when 77Se-enriched sodium selenate (Sefert) was applied to the leaves at a rate of 3.33 μg Se per kg soil (equivalent to 10 g ha−1) and two growth stages, namely stem elongation, Zadoks stage 31/32 (GS1), and heading stage, Zadoks stage 57 (GS2). The effect of urea inclusion in foliar Se fertilisers on the penetration rates of Se was also investigated. Wheat was harvested at 3, 10, and 17 days and 3, 10, and 34 days after Se applications at GS1 and GS2, respectively. Applying foliar Se, irrespective of the formulation, brought grain Se concentration to a level high enough to be considered adequate for biofortification. Inclusion of N in the foliar Se solution applied at an early growth stage increased recoveries in the plants, likely due to improved absorption of applied Se through the young leaves. At a later growth stage, the inclusion of N in foliar Se solutions was also beneficial as it improved the assimilation of applied inorganic Se into bioavailable selenomethionine, which was then rapidly translocated to the grain. The practical knowledge gained about the optimisation of Se fertiliser formulation, method, and timing of application will be of importance in refining biofortification programs across different climatic regimes

    Author Correction: Improving the efficacy of selenium fertilizers for wheat biofortification

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    Correction to: Scientific Reports https://doi.org/10.1038/s41598-019-55914-0, published online 20 December 201

    Leaching of cadmium and zinc from Spodosols: from laboratory to field scale

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    Sulfur Uptake from Fertilizer Fortified with Sulfate and Elemental S in Three Contrasting Climatic Zones

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    Field trials with labeled fertilizers can be used to provide information on fertilizer efficiency, residual value, and nutrient fate. We assessed the uptake from elemental S (ES) and sulfate S (SO4-S) in S-fortified monoammonium phosphate fertilizers by various crops at three sites in Argentina, Brazil, and Canada. The S sources were labeled with 34S, and the 34S abundance in the plant tissue was analyzed at an early stage and at maturity over two consecutive years. At the sites in Argentina and Canada, the recovery of ES in the crop was smaller than that of SO4-S in the first year, while the opposite was true in the second year. At the Brazilian site, the recovery of ES was similar to that of SO4-S in the first year, but higher in the second year. In the Argentina and Canada sites, the cumulative recovery of SO4-S was >65% and that of ES was 20−25%. In the Brazilian site, the cumulative recovery of SO4-S was 9% and that of ES 16%. The higher recovery of ES than of SO4-S in the Brazilian site was attributed to leaching of added SO4-S and relatively fast oxidation of ES due to the warm climate. These results suggest that ES may be more suitable than SO4-S as a fertilizer S source in warm humid climates, while inclusion of SO4-S in the fertilizer is recommended in colder climates as slow oxidation limits the initial availability of ES

    Kinetic speciation of metal complexes in relation to metal mobility in soils

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