peer reviewed | Microplastic contamination is an emerging issue in the marine environment including the Arctic. However, the occurrence of microplastics in the Arctic fjords remains less understood. Sample collections were conducted by trawling horizontally in surface water (0-0.4-m depth) and trawling vertically in the water column (0-200-m depth) to investigate the abundance, composition, and distribution of microplastics in the Rijpfjorden, Northern Svalbard, in the summer of 2017. Laser Direct Infrared chemical imaging technique was applied for the counting and identification of microplastic particles. A total of 1010 microplastic particles and 14 mesoplastics were identified from 41,038 particles in eight samples from the Rijpfjorden. The abundance of microplastics larger than 300 µm was 0.15 ± 0.19 n/m3 in surface water, and 0.15 ± 0.03 n/m3 in the water column of the Rijpfjorden. The microplastic particles identified in Rijpfjorden water consisted of 10 types of polymers. The dominant microplastics are polyurethane, polyethylene, polyvinyl acetate, polystyrene, polypropylene, and alkyd varnish. Historical ship activities and newly melted sea ice might be major sources of microplastics in the seawater of Rijpfjorden. In general, contamination of microplastics larger than 300 µm in Rijpfjorden water is at a low level in comparison to other polar waters. Further research is needed to confirm the origin and fate of microplastics below 300 µm in Arctic fjords.

The redox speciation of iron was determined during the iron fertilization LOHAFEX and for the first time, the chemiluminescence assay of filtered and unfiltered samples was systematically compared. We hypothesize that higher chemiluminescence in unfiltered samples was caused by Fe(II) adsorbed onto biological particles. Dissolved and particulate Fe(II) increased in the mixed layer steadily 6-fold during the first two weeks and decreased back to initial levels by the end of LOHAFEX. Both Fe(II) forms did not show diel cycles downplaying the role of photoreduction. The chemiluminescence of unfiltered samples across the patch boundaries showed strong gradients, correlated significantly to biomass and the photosynthetic efficiency and were higher at night, indicative of a biological control. At 150 m deep, a secondary maximum of dissolved Fe(II) was associated with maxima of nitrite and ammonium despite high oxygen concentrations. We hypothesize that during LOHAFEX, iron redox speciation was mostly regulated by trophic interactions.

International audience | Temperature is a key factor that influences pesticide degradation. Extrapolating degradation half-lives (DT50) measured at a given temperature to different temperatures remains challenging, especially for tropical conditions with high temperatures. In this study, the use of the standard Arrhenius equation for correcting temperature effects on pesticide degradation in soils was evaluated and its performance was compared with that of alternative Arrhenius-based equations. To do so, a database of 509 DT50 values measured between 5 and 35 °C for 32 pesticides on tropical and temperate soils was compiled for the first time through an extensive literature search. The temperature correction models were fitted to the database using linear mixed regression approaches that included soil type and compound effects. No difference in the temperature dependence of DT50 between tropical and temperate soils was detected, regardless of the model. A comparison of the prediction performances of the models showed that constant activation energy (Ea) cannot be considered valid for the whole range of temperatures. The classical Arrhenius equation with an Ea of 65.4 kJ.mol−1, as recommended by the European Food Safety Authority (EFSA), was shown to be valid for correcting the DT50 only for temperatures ranging from 5 to 20 °C. However, for temperatures greater than 20 °C, which are common in tropical environments, the median Ea was significantly lower at 10.3 kJ.mol−1. These findings suggest the need to adapt the standard temperature correction of the European pesticide risk assessment temperature procedure when it is applied in tropical settings

International audience | It is essential to monitor pesticides in soils as their presence at trace levels and their bioavailability can induce adverse effects on soil's ecosystems, animals, and human health. In this study, we developed an analytical method for the quantification of traces of multi-class pesticides in soil using liquid chromatography-tandem mass spectrometry. In this way, 31 pesticides were selected, including 12 herbicides, 9 insecticides, and 10 fungicides. Two extraction techniques were first evaluated namely: the pressurized liquid extraction and the QuEChERS procedure. The latest one was finally selected and optimized, allowing extraction recoveries of 55 to 118 %. The addition of the chelating agent EDTA, which binds preferentially to soil cations that complex some pesticides, facilitates their extraction. Coupled with liquid chromatography-tandem mass spectrometry, the procedure displayed very high sensitivity, with limits of quantification (LOQ) in the range 0.01-5.5 ng/g. A good linearity (R² >0.992) was observed over two orders of magnitude (LOQ-100×LOQ) with good accuracy (80%-120 %) for all compounds except the two pyrethroids lambda-cyhalothrin and tau-fluvalinate (accuracy comprised between 50 and 175%) and the cyclohexanedione cycloxydim (accuracy<35%). Good repeatability and reproducibility were also achieved. The method was finally successfully applied to 12 soil samples collected from 3 land-use types. Among the 31-targeted pesticides, 24 were detected at least once, with concentration levels varying from LOQ to 722 ng/g. Many values were below 0.5 ng/g, indicating that the developed method could provide new knowledge on the extremely low residual contents of some pesticides.

International audience | The research paper is aimed to modify the human health impact assessment of Cr in soils. The current article presents the input of several critical parameters for the human health Impact Score (IShum) assessment in soils. The modification of the IShum is derived using geological data — results of neutron activation analysis of soils are used in the IShum calculation; research area is divided using the watersheds and population size and density. Watersheds reflect the local environmental conditions of the territory unlike the administrative units (geographical areas of the studied region) due to their geological independence. The calculations of the characterization factor value underestimate the influence of the population size and density on the final result. Default characterization factor values cannot be considered during the assessment of the potential human health impact for the big sparsely inhabited areas. In case of very low population density, the result will be overrated and underestimated in the opposite case. The current approach demonstrates that the geographical separation in the USEtox model should be specified. The same approach can be utilized for other geo zones due to the accessibility of this information (area size, population size, and density, geological, and landscape features). | The research paper is aimed to modify the human health impact assessment of Cr in soils. The current article presents the input of several critical parameters for the human health Impact Score ( IShum) assessment in soils. The modification of the IShum is derived using geological data — results of neutron activation analysis of soils are used in the IShum calculation; research area is divided using the watersheds and population size and density. Watersheds reflect the local environmental conditions of the territory unlike the administrative units (geographical areas of the studied region) due to their geological independence. The calculations of the characterization factor value underestimate the influence of the population size and density on the final result. Default characterization factor values cannot be considered during the assessment of the potential human health impact for the big sparsely inhabited areas. In case of very low population density, the result will be overrated and underestimated in the opposite case. The current approach demonstrates that the geographical separation in the USEtox model should be specified. The same approach can be utilized for other geo zones due to the accessibility of this information (area size, population size, and density, geological, and landscape features).

International audience | It is essential to monitor pesticides in soils as their presence at trace levels and their bioavailability can induce adverse effects on soil's ecosystems, animals, and human health. In this study, we developed an analytical method for the quantification of traces of multi-class pesticides in soil using liquid chromatography-tandem mass spectrometry. In this way, 31 pesticides were selected, including 12 herbicides, 9 insecticides, and 10 fungicides. Two extraction techniques were first evaluated namely: the pressurized liquid extraction and the QuEChERS procedure. The latest one was finally selected and optimized, allowing extraction recoveries of 55 to 118 %. The addition of the chelating agent EDTA, which binds preferentially to soil cations that complex some pesticides, facilitates their extraction. Coupled with liquid chromatography-tandem mass spectrometry, the procedure displayed very high sensitivity, with limits of quantification (LOQ) in the range 0.01-5.5 ng/g. A good linearity (R² >0.992) was observed over two orders of magnitude (LOQ-100×LOQ) with good accuracy (80%-120 %) for all compounds except the two pyrethroids lambda-cyhalothrin and tau-fluvalinate (accuracy comprised between 50 and 175%) and the cyclohexanedione cycloxydim (accuracy<35%). Good repeatability and reproducibility were also achieved. The method was finally successfully applied to 12 soil samples collected from 3 land-use types. Among the 31-targeted pesticides, 24 were detected at least once, with concentration levels varying from LOQ to 722 ng/g. Many values were below 0.5 ng/g, indicating that the developed method could provide new knowledge on the extremely low residual contents of some pesticides.

International audience | The Telesphore project aims to identify and to quantify the transfers of pharmaceuticals residues and biocides and their related processes from biosolids and manure spread on grassland as fertilizers. Real land-spreading conditions were reproduced on six in-situ lysimeters and the pathway of pharmaceuticals and biocides was tracked by sampling infiltrated water and soil over one year. The study has focused on 32 pharmaceuticals, biocides and their transformation products, selected from their previous detection in several organic fertilizers. Six months after biosolids and manure spreading, the soil concentrations were in the range of nanograms per gram of soil and only few compounds were detected in infiltrated water. Ketoprofen was found to be the most mobile and persistent pharmaceutical compound after biosolids application whereas thiabendazole was the most frequently detected substance in infiltrated water after manure amendment.