EUSEDcollab: a network of data from European catchments to monitor net soil erosion by water.

As a network of researchers we release an open-access database (EUSEDcollab) of water discharge and suspended sediment yield time series records collected in small to medium sized catchments in Europe. EUSEDcollab is compiled to overcome the scarcity of open-access data at relevant spatial scales for studies on runoff, soil loss by water erosion and sediment delivery. Multi-source measurement data from numerous researchers and institutions were harmonised into a common time series and metadata structure.

Trapped microplastics within vertical redeposited sediment: Experimental study simulating lake and channeled river systems during resuspension events.

Plastic waste and its fragments (microplastics; <5 mm) have been observed in almost all types of environments. However, the mechanisms underlying the flow and transport processes of plastics are unknown. This is particularly valid for river sediments, where complex interactions occur between particles and influence their vertical and horizontal distribution patterns.

Extraction of microplastics from sediment matrices: Experimental comparative analysis.

Microplastics are small (<5 mm) fragments of plastic debris that are ubiquitous in oceans and terrestrial ecosystems. Studies on microplastics in sediment and soil matrices are particularly challenging because of the need to separate the plastics from the sediments. We investigated the efficiencies of 18 combinations of six extracting solutions (ESs) (oil, water, oil-in-water, NaCl, oil-in-NaCl, and NaI) and three isolation methods (IMs) (hand stirring, centrifugation, and aeration) for fine and coarse sediments, with low and high density polymers.

To What Extent Can Micro- and Macroplastics Be Trapped in Sedimentary Particles? A Case Study Investigating Dredged Sediments.

Plastic wastes and their fragments (microplastics, MPs < 5 mm) represent a global, persistent, and ubiquitous threat to ecosystems. Their sources, transfers, and fates are still poorly understood, especially in rivers. To fill this gap, sediments were collected from two dredging disposal sites along the Aa River (France).

Environmental availability and oral bioaccessibility of Cd and Pb in anthroposols from dredged river sediments.

Dredging and disposal of sediments onto land sites is a common practice in urban and industrial areas that can present environmental and health risks when the sediments contain metallic elements. The aim of this study was to characterise and study the environmental and toxicological availability of Cd and Pb in anthroposols from dredged river sediments. To do this, 67 surface samples spread over 12 sediment disposal sites in northern France were studied.

Assessing temporal variability and controlling factors of the sediment budget of a small agricultural catchment in Northern France (the Pommeroye).

A high-frequency monitoring station was implemented at the outlet of the small catchment of the Pommeroye (0.54 km) in Northern France to study erosion by runoff and hydro-sedimentological responses to heavy rainfall events in the context of Quaternary loess deposits. The aim of this experimental work is to assess the temporal variability of sediment yield and to identify the factors controlling the hydro-sedimentary response.

Quantification of tributaries contributions using a confluence-based sediment fingerprinting approach in the Canche river watershed (France).

Since a few years, land use management aims to reduce and control water erosion processes in watersheds but there is a lack of quantitative information on the contribution of the sources of transported sediment. This is most important in agricultural areas where soils are sensitive to erosion. The geology of these areas is often characterized by large expanses of relatively homogeneous quaternary silts.

Analyzing the uncertainty of diffusive gel-based passive samplers as tools for evaluating the averaged contamination of surface water by organic pollutants.

Agarose gel-based passive samplers are nowadays one of the most effective sampling devices able to provide a quantitative evaluation of water contamination level for a broad range of organic contaminants. These devices show significant improvements in comparison to the previous passive samplers dedicated to hydrophilic compounds because they tend to reduce the effect of hydrodynamic flow conditions on the uptake rate of compounds and thus subsequently to improve their accuracy. However, albeit their effects minimized, hydrodynamic water flow and temperature are reported as variables likely to change the uptake rate of compounds that may lead to some inaccuracy if they are not adequately taken into account.

Understanding and predicting the diffusivity of organic compounds in polydimethylsiloxane material for passive sampler applications using a simple quantitative structure-property relationship model.

The diffusivity of 145 compounds in polydimethylsiloxane (PDMS) material was determined in the laboratory using a film stacking technique. The results were pooled with available literature data, providing a final data set of 198 compounds with diffusivity (D ) spanning over approximately 5 log units. The principal variables controlling the diffusivity of penetrants were investigated by comparing D within and between different homologous series.

Near-surface distribution of pollutants in coastal waters as assessed by novel polyethylene passive samplers.

We report a novel and inexpensive method to provide high resolution vertical measurements of temporally integrated organic contaminants in surface and sub-surface waters in polluted coastal environments. It employs a strip of polyethylene deployed as a passive sampler. Verifications are confirmed via conventional spot sample analyses and against Performance Reference Compound (PRC) calibration methods.

Calibration and response of an agarose gel based passive sampler to record short pulses of aquatic organic pollutants.

A passive sampler inspired from previous devices was developed for the integrative sampling of a broad range of contaminants in the water column. Our primary objective was to improve the performance of the device to provide accurate and averaged pollutant water concentrations. For this purpose, an agarose diffusive gel was used as the boundary layer that drives the analyte uptake rate.

Assessing the transport of PAH in the surficial sediment layer by passive sampler approach.

A new method based on passive samplers has been developed to assess the diffusive flux of fluorene, fluoranthene and pyrene in the sediment bed and across the sediment-water interface. The dissolved compound concentration gradient in the sediment in the vertical direction was measured at the outlet of a storm water pond by using polyethylene strips as passive samplers. Simultaneously, the dissipation of a set of tracer compounds preloaded in the passive samplers was measured to estimate the effective diffusion coefficients of the pollutants in the sediment.

A new application of passive samplers as indicators of in-situ biodegradation processes.

In this paper, a method for evaluating the in-situ degradation of nitro polycyclic aromatic hydrocarbons (nitro-PAH) in sediments is presented. The methodology is adapted from the passive sampler technique, which commonly uses the dissipation rate of labeled compounds loaded in passive sampler devices to sense the environmental conditions of exposure. In the present study, polymeric passive samplers (made of polyethylene strips) loaded with a set of labeled polycyclic aromatic hydrocarbons (PAH) and nitro-PAH were immersed in sediments (in field and laboratory conditions) to track the degradation processes.

Relationship between the water-exchangeable fraction of PAH and the organic matter composition of sediments.

The sorption of PAH on 12 different sediments was investigated and was correlated to their corresponding organic matter (OM) content and quality. For this purpose, the OM was precisely characterized using thermal analysis consisting in the successive combustion and quantification of the increasingly thermostable fractions of the OM. Simultaneously, the water-exchangeable fraction of the sorbed PAH defined as the amount of PAH freely exchanged between the water and the sediment (by opposition to the PAH harshly sorbed to the sediments particles) was determined using a passive sampler methodology recently developed.

Thickness and material selection of polymeric passive samplers for polycyclic aromatic hydrocarbons in water: Which more strongly affects sampler properties?

Three configurations of single-phase polymer passive samplers made of polyoxymethylene (POM), silicone rubber, and polyethylene (PE) were simultaneously calibrated in laboratory experiments by determining their partitioning coefficients and the POM diffusion coefficients and by validating a kinetic accumulation model. In addition, the performance of each device was evaluated under field conditions. With the support of the developed model, the device properties are discussed with regard to material selection and polymer thickness.

Simulation of aromatic polycyclic hydrocarbons remobilization from a river sediment using laboratory experiments supported by passive sampling techniques.

Resuspension of bedded sediments was simulated under laboratory-controlled conditions in order to assess the amount of polycyclic aromatic hydrocarbons (PAH) remobilized in the dissolved fraction during one short and vigorous mixing. The desorbed amount of PAH was compared to the exchangeable fraction, the total amount of PAH sorbed on the sediment particles, and the dissolved PAH amount contained in the interstitial pore waters in order to evaluate the contribution of each fraction to the total amount of PAH released. To monitor the desorption of PAH and measure low trace level concentrations, passive samplers were used in an experimental open flow through exposure simulator.

Factorial Kriging Analysis as a tool for explaining the complex spatial distribution of metals in sediments.

Rivers flowing through urbanized and industrial areas are usually greatly damaged by anthropogenic activities discharging contaminants. Characterizing the spatial distribution of pollutants in sediments is of high importance for selecting a suitable remediation operation, but is a complex task because this spatial variability is the result of various physical and chemical mechanisms occurring at different scales. Factorial Kriging Analysis (FKA) was applied on data collected in a canalized river (Scarpe, France) for that purpose, because this geostatistical technique allows to decompose a given variable into components of different spatial correlations and map them separately.