Plastic debris accumulated on Sargassum algae stranded biomass are vectors for different As(V) and As(III) forms.

This work shows that the plastic debris accumulated along with stranded Sargassum biomass in Guadeloupe's beaches contains different forms of arsenic. Results from synchrotron nano X-ray Fluorescence (nanoXRF) and nano X-ray Absorption Near Edge Structure (nanoXANES) show that arsenate (As(V) in a tetrahedral coordination) present in seawater is complexed in the algae cell walls in an octahedral As(V) form, which is subsequently reduced to As(III) within the algae. Inorganic As(III) is either excreted or may undergo methylation and/or binding to glutathione, which is then stored in the algal cells or excreted.

Trophic transfer effects of PS nanoplastics and field-derived nanoplastics in the freshwater clam Corbicula fluminea.

Plastic pollution is of global concern. Many studies investigated the effect of micro and nanoplatics towards aquatic organisms. However, relatively few studies were assessed on freshwater organisms.

Nano(micro)plastic mobility in soil: Metallic additives and Sr isotopes as potential tracers.

Metal contaminants were found in a soil amended with a compost produced from household waste that included plastic debris. A strong correlation between the microplastics (MPs) distribution and the metal concentrations in the soil profile. Metals in the highest concentrations corresponded to the most significant plastic additives.

Toxicity of environmental and polystyrene plastic particles on the bivalve Corbicula fluminea: focus on the molecular responses.

Among aquatic organisms, filter feeders are particularly exposed to the ingestion of microplastics (MPs) and nanoplastics (NPs). The present study investigates the effect of environmental microplastics (ENV MPs) and nanoplastics (ENV NPs) generated from macro-sized plastic debris collected in the Garonne River (France), and polystyrene NPs (PS NPs) on the freshwater bivalve Corbicula fluminea. Organisms were exposed to plastic particles at three concentrations: 0.

Toxicity assessment of environmental MPs and NPs and polystyrene NPs on the bivalve Corbicula fluminea using a multi-marker approach.

Small plastic particles, microplastics (MPs) and nanoplastics (NPs) represent a major threat in aquatic environments. Freshwater organisms are exposed to MPs and NPs, particularly in industrial and urban areas. The present study aimed to compare the toxicity between polystyrene NPs (PS NPs) and environmental microplastics (ENV MPs) and nanoplastics (ENV NPs) generated from macro-sized debris collected in the Garonne River on the freshwater bivalve C.

The environmental fate of nanoplastics: What we know and what we need to know about aggregation.

The presence of nanoplastics in the environment has been proven. There is now an urgent need to determine how nanoplastics behave in the environment and to assess the risks they may pose. Here, we examine nanoplastic homo- and heteroaggregation, with a focus on environmentally relevant nanoplastic particle models.

Continuum from microplastics to nanoplastics: effects of size and source on the estuarine bivalve Scrobicularia plana.

Plastic has been largely detected in estuarine environments and represents major concern towards aquatic living organisms. The present study evaluates the impact of microplastics (MPs) and nanoplastics (NPs) under realistic exposure conditions. Scrobicularia plana individuals were exposed to low concentrations (0.

Effect of size continuum from nanoplastics to microplastics on marine mussel Mytilus edulis: Comparison in vitro/in vivo exposure scenarios.

For several decades, plastic has been a global threat in terms of pollution. Plastic polymers, when introduce in the aquatic environment, are exposed to fragmentation processes into microplastics (MPs) and nanoplastics (NPs) which could potentially interact with living organisms. The objective of this work was to study the effects of plastic particles representative of those found in the environment, on the marine mussels Mytilus edulis, under two exposure scenarios: in vivo and in vitro.

Implications of speciation on rare earth element toxicity: A focus on organic matter influence in Daphnia magna standard test.

Rare earth elements (REE) have become essential in high- and green-technologies. Their increasing use lead to the release of anthropogenic REE into the environment including aquatic systems. The limited data available on the aquatic ecotoxicology of REE indicate their biological effects are highly dependent on their speciation, posing challenges for a reliable environmental risk assessment (ERA).

Metals in microplastics: determining which are additive, adsorbed, and bioavailable.

Microplastics from the North Atlantic Gyre deposited on Guadeloupe beaches were sampled and characterized. A new method is developed to identify which elements were present as additives in these microplastics. The method used both acidic leaching and acidic digestion.

How crucial is the impact of calcium on the reactivity of iron-organic matter aggregates? Insights from arsenic.

Environmental iron-organic matter (Fe-OM) aggregates play a major role in the dynamic of pollutants. Nowadays, there is a lack of information about the control exerted by their structural organization on their reactivity towards metal(loid)s and in particular, the impact of major ions, such as calcium. The sorption capacity of mimetic environmental Fe-OM-Ca aggregates was investigated relative to the Fe/organic carbon (OC) and Ca/Fe ratios using As as a probe.

Coupled As and Mn Redox Transformations in an Fe(0) Electrocoagulation System: Competition for Reactive Oxidants and Sorption Sites.

Iron electrocoagulation (EC) can be used for the decentralized treatment of arsenic(As)-contaminated groundwater. Iron EC involves the electrolytic dissolution of an Fe(0) electrode to Fe(II). This process produces reactive oxidants, which oxidize As(III) and Fe(II) to As(V) and a range of Fe(III) (oxyhydr)oxide phases.

Oxidation of Fe(II)-Organic Matter Complexes in the Presence of the Mixotrophic Nitrate-Reducing Fe(II)-Oxidizing Bacterium Acidovorax sp. BoFeN1.

Fe(II)-organic matter (Fe(II)-OM) complexes are abundant in the environment and may play a key role for the behavior of Fe and pollutants. Mixotrophic nitrate-reducing Fe(II)-oxidizing bacteria (NRFeOx) reduce nitrate coupled to the oxidation of organic compounds and Fe(II). Fe(II) oxidation may occur enzymatically or abiotically by reaction with nitrite that forms during heterotrophic denitrification.

Tracing platinum accumulation kinetics in oyster Crassostrea gigas, a sentinel species in coastal marine environments.

Platinum Group Elements (PGEs) are extremely scarce in the Earth's Crust and of strong interest for high-end technologies due to their specific properties. They belong to the Technology Critical Elements (TCEs) for which use is forecast to increase, implying growing emissions into the environment in the following years. In particular, with the intensive use of platinum (Pt) in car catalytic converters, the anthropogenic geochemical cycle of this element has surpassed the natural cycle.

Does As(III) interact with Fe(II), Fe(III) and organic matter through ternary complexes?

Up until now, only a small number of studies have been dedicated to the binding processes of As(III) with organic matter (OM) via ionic Fe(III) bridges; none was interested in Fe (II). Complexation isotherms were carried out with As(III), Fe(II) or Fe(III) and Leonardite humic acid (HA). Although PHREEQC/Model VI, implemented with OM thiol groups, reproduced the experimental datasets with Fe(III), the poor fit between the experimental and modeled Fe(II) data suggested another binding mechanism for As(III) to OM.

Thiol groups controls on arsenite binding by organic matter: new experimental and modeling evidence.

Although it has been suggested that several mechanisms can describe the direct binding of As(III) to organic matter (OM), more recently, the thiol functional group of humic acid (HA) was shown to be an important potential binding site for As(III). Isotherm experiments on As(III) sorption to HAs, that have either been grafted with thiol or not, were thus conducted to investigate the preferential As(III) binding sites. There was a low level of binding of As(III) to HA, which was strongly dependent on the abundance of the thiols.