Degradation study of δ-hexachlorocyclohexane by iron sulfide nanoparticles: Elucidation of reaction pathway using compound specific isotope analysis and pH variation.

pH influences the reactivity of iron (II) minerals towards halogenated pollutants like hexachlorocyclohexanes (HCHs). To explore these incompletely understood interactions, we investigated the carbon isotope fractionation of the δ-HCH isomer during dehalogenation by iron sulfide at pHs spanning a pH range across slightly acidic to alkaline domains (5.8-9.

Comparative analysis of microplastics detection methods applied to marine sediments: A case study in the Bay of Marseille.

An intercomparison exercise on "microplastics in sediment" was carried out by five laboratories using samples collected in the Bay of Marseille in September 2021. The results from different extraction and identification methods varied depending on the type and size classes of MPs, and was better than 80 % for the size class >300 μm and for the fragments. The variability in recovery rates can be attributed to the choice of reagents and extraction protocols.

Temporal trajectories of artificial radiocaesium Cs in French rivers over the nuclear era reconstructed from sediment cores.

Cs is a long-lived man-made radionuclide introduced in the environment worldwide at the early beginning of the nuclear Era during atmospheric nuclear testing's followed by the civil use of nuclear energy. Atmospheric fallout deposition of this major artificial radionuclide was reconstructed at the scale of French large river basins since 1945, and trajectories in French nuclearized rivers were established using sediment coring. Our results show that Cs contents in sediments of the studied rivers display a large spatial and temporal variability in response to the various anthropogenic pressures exerted on their catchment.

Experimental and Theoretical Study of the OH-Initiated Degradation of Piperidine under Simulated Atmospheric Conditions.

The OH-initiated photo-oxidation of piperidine and the photolysis of 1-nitrosopiperidine were investigated in a large atmospheric simulation chamber and in theoretical calculations based on CCSD(T*)-F12a/aug-cc-pVTZ//M062X/aug-cc-pVTZ quantum chemistry results and master equation modeling of the pivotal reaction steps. The rate coefficient for the reaction of piperidine with OH radicals was determined by the relative rate method to be = (1.19 ± 0.

Stable isotope composition of pesticides in commercial formulations: The ISOTOPEST database.

By assessing the changes in stable isotope compositions within individual pesticide molecules, Compound Specific Isotope Analysis (CSIA) holds the potential to identify and differentiate sources and quantify pesticide degradation in the environment. However, the environmental application of pesticide CSIA is limited by the general lack of knowledge regarding the initial isotopic composition of active substances in commercially available formulations used by farmers. To address this limitation, we established a database aimed at cataloguing and disseminating isotopic signatures in commercial formulations to expand the use of pesticide CSIA.

Experimental determination of the partitioning of representative organic pollutants to the air-water interface.

Using glancing-angle laser-induced fluorescence (GALIF) spectroscopy as a probe, the partitioning of naphthalene, fluoranthene, pyrene, umbelliferone, phenol red, and bisphenol A from bulk solution to the air-water interface was examined in both pure water and aqueous solutions of 6 mM octanol. Previous studies provided similar Langmuir adsorption isotherms for anthracene and imidazole 2-carboxaldehyde. The surface partitioning behaviour of each compound in both environments was well described using a Langmuir adsorption model; partitioning coefficients were derived from the fits to such isotherms.

A Novel Multi-ion Evaluation Scheme to Determine Stable Chlorine Isotope Ratios (Cl/Cl) of Chlordecone by LC-QTOF.

Organochlorinated pesticides are highly persistent organic pollutants having important adverse effects in the environment. To study their fate, compound-specific isotope analysis (CSIA) may be used to investigate their degradation pathways and mechanisms but is currently limited to C isotope ratios. The assessment of Cl isotope ratios from mass spectra is complicated by the large number of isotopologues of polychlorinated compounds.

Sensitivity of pollutant concentrations in urban streets to asphalt and traffic-related emissions.

The higher concentrations of atmospheric particles, such as black carbon (BC) and organic matter (OM), detected in streets compared to the urban background are predominantly attributed to road traffic. The integration of this source of pollutant in air quality models nevertheless entails a high degree of uncertainty and some other sources may be missing. Through sensitivity scenarios, the impacts on pollutant concentrations of sensitivities related to traffic and road-asphalt emissions are evaluated.

Chlorinated solvents source identification by nonlinear optimization method.

In this work, chloride ions were used as conservative tracers and supplemented with conservative amounts of chloroethenes (PCE, TCE, Cis-DCE, 1,1-DCE), chloroethanes (1,1,1-TCA, 1,1-DCA), and the carbon isotope ratios of certain compounds, the most representative on the sites studied, which is a novelty compared to the optimization methods developed in the scientific literature so far. A location of the potential missing sources is then proposed in view of the balances of the calculated mixing fractions. A test of the influence of measurement errors on the results shows that the uncertainties in the calculation of the mixture fractions are less than 11%, indicating that the source identification method developed is a robust tool for identifying sources of chlorinated solvents in groundwater.

Stable carbon and hydrogen isotope fractionation of volatile organic compounds caused by vapor-liquid equilibrium.

Several types of laboratory experiments were conducted to evaluate isotope fractionation caused by phase transfer process for a selection of common environmental contaminants. Carbon and hydrogen isotope fractionation caused by vaporization of non-aqueous phase liquid (NAPL), by volatilization from water and by dissolution into an organic solvent (tetraethylene glycol dimethylether or TGDE) under equilibrium conditions was investigated with closed system experimental setups to isolate the air-liquid partitioning process. A selection of aromatic, aliphatic and chlorinated compounds along with one fuel oxygenate (methyl tert-butyl ether or MTBE) were evaluated to determine isotope enrichment factor related to respective phase transfer process.

One Health surveillance of West Nile and Usutu viruses: a repeated cross-sectional study exploring seroprevalence and endemicity in Southern France, 2016 to 2020.

BackgroundWest Nile virus (WNV) and Usutu virus (USUV), two closely related flaviviruses, mainly follow an enzootic cycle involving mosquitoes and birds, but also infect humans and other mammals. Since 2010, their epidemiological situation may have shifted from irregular epidemics to endemicity in several European regions; this requires confirmation, as it could have implications for risk assessment and surveillance strategies.AimTo explore the seroprevalence in animals and humans and potential endemicity of WNV and USUV in Southern France, given a long history of WNV outbreaks and the only severe human USUV case in France in this region.

Detailed Speciation of Non-Methane Volatile Organic Compounds in Exhaust Emissions from Diesel and Gasoline Euro 5 Vehicles Using Online and Offline Measurements.

The characterization of vehicle exhaust emissions of volatile organic compounds (VOCs) is essential to estimate their impact on the formation of secondary organic aerosol (SOA) and, more generally, air quality. This paper revises and updates non-methane volatile organic compounds (NMVOCs) tailpipe emissions of three Euro 5 vehicles during Artemis cold urban (CU) and motorway (MW) cycles. Positive matrix factorization (PMF) analysis is carried out for the first time on proton transfer reaction time-of-flight mass spectrometer (PTR-ToF-MS) datasets of vehicular emission.

Molecular assessment of Theileria equi and Babesia caballi prevalence in horses and ticks on horses in southeastern France.

Equine piroplasmosis (EP) is a tick-borne disease caused by Babesia caballi and Theileria equi that is potentially emerging in non-endemic countries. We conducted a descriptive study to investigate EP prevalence and spatial distribution in an endemic region: the Camargue and the Plain of La Crau in France. In spring 2015 and 2016, we carried out sampling at stables (total n = 46) with a history of horses presenting chronic fever or weight loss.

Using 1,1,1-Trichloroethane degradation data to understand NAPL dissolution and solute transport at real sites.

Analytical and numerical models describing the evolution of contaminant concentrations in the plume associated with the dissolution of NAPL source and degradation processes were presented in the literature. At real sites and particularly in complex aquifers like chalk, it is difficult to understand how the sources of contaminants evolve with time. 1,1,1-Trichloroethane (1,1,1-TCA) is one of the few compounds with a well-known hydrolysis constant, that can help to improve knowledge of the contaminant sources and transport rates of dissolved contaminants in groundwater by dating the spill.

Dehalogenation of α-hexachlorocyclohexane by iron sulfide nanoparticles: Study of reaction mechanism with stable carbon isotopes and pH variations.

The biodegradation of hexachlorocyclohexanes (HCHs) is known to be accompanied by isotope fractionation of carbon (C/C), but no systematic studies were performed on abiotic degradation of HCH isomers by iron (II) minerals. In this study, we explored the carbon isotope fractionation of α-HCH during dechlorination by FeS nanoparticles at different pH values. The results of three different experiments showed that the apparent rate constants during dehalogenation of α-HCH by FeS increased with pH.

Atmospheric Chemistry of 2-Amino-2-methyl-1-propanol: A Theoretical and Experimental Study of the OH-Initiated Degradation under Simulated Atmospheric Conditions.

The OH-initiated degradation of 2-amino-2-methyl-1-propanol [CHC(NH)(CH)CHOH, AMP] was investigated in a large atmospheric simulation chamber, employing time-resolved online high-resolution proton-transfer reaction-time-of-flight mass spectrometry (PTR-ToF-MS) and chemical analysis of aerosol online PTR-ToF-MS (CHARON-PTR-ToF-MS) instrumentation, and by theoretical calculations based on M06-2X/aug-cc-pVTZ quantum chemistry results and master equation modeling of the pivotal reaction steps. The quantum chemistry calculations reproduce the experimental rate coefficient of the AMP + OH reaction, aligning () = 5.2 × 10 × exp (505/) cm molecule s to the experimental value = 2.

Effect of NAPL mixture and alteration on Rn partitioning coefficients: Implications for NAPL subsurface contamination quantification.

Soils and groundwater are often contaminated by complex organic mixtures also called Non Aqueous Phase Liquids (NAPLs). Several techniques such as drilling, monitoring of soil gas or injection of tracers are traditionally used to quantify NAPLs in aquifers but are complex to perform. The use of natural soil gas such as Rn could be an easy and cheap alternative.

Intramolecular non-covalent isotope effects at natural abundance associated with the migration of paracetamol in solid matrices during liquid chromatography.

Position-specific isotope analysis by Nuclear Magnetic Resonance spectrometry was employed to study the C intramolecular isotopic fractionation associated with the migration of organic substrates through different stationary phases chromatography columns. Liquid chromatography is often used to isolate compounds prior to their isotope analysis and this purification step potentially alters the isotopic composition of target compounds introducing a bias in the later measured data. Moreover, results from liquid chromatography can yield the sorption parameters needed in reactive transport models that predict the transport and fate of organic contaminants to in the environment.

Experimental and Theoretical Study of the OH-Initiated Degradation of Piperazine under Simulated Atmospheric Conditions.

The OH-initiated photo-oxidation of piperazine and 1-nitropiperazine as well as the photolysis of 1-nitrosopiperazine were investigated in a large atmospheric simulation chamber. The rate coefficient for the reaction of piperazine with OH radicals was determined by the relative rate method to be = (2.8 ± 0.

Quantification of Lambda (Λ) in multi-elemental compound-specific isotope analysis.

In multi-elemental compound-specific isotope analysis the lambda (Λ) value expresses the isotope shift of one element versus the isotope shift of a second element. In dual-isotope plots, the slope of the regression lines typical reveals the footprint of the underlying isotope effects allowing to distinguish degradation pathways of an organic contaminant molecule in the environment. While different conventions and fitting procedures are used in the literature to determine Λ, it remains unclear how they affect the magnitude of Λ.

Nitrous acid formation on Zea mays leaves by heterogeneous reaction of nitrogen dioxide in the laboratory.

Nitrous acid (HONO) is of considerable interest because it is an important precursor of hydroxyl radicals (OH), a key species in atmospheric chemistry. HONO sources are still not well understood, and air quality models fail to predict OH as well as HONO mixing ratios. As there is little knowledge about the potential contribution of plant surfaces to HONO emission, this laboratory work investigated HONO formation by heterogeneous reaction of NO on Zea mays.

Functional Trait-Based Screening of Zn-Pb Tolerant Wild Plant Species at an Abandoned Mine Site in Gard (France) for Rehabilitation of Mediterranean Metal-Contaminated Soils.

The selection of plant species at mine sites is mostly based on metal content in plant parts. Recent works have proposed referring to certain ecological aspects. However, plant traits for plant metal-tolerance still need to be accurately assessed in the field.

Rapid on site assessment of a compost chemical stability parameter by UV and fluorescence spectroscopy coupled with mathematical treatment.

Sewage sludges are problematic due to the constant increase of urban population. The high level of organic matter in sludges can be valorized by co-composting with green waste. Many chemical changes occur in the compost maturation process, resulting on stabilized organic matter by humification which is recoverable as soil amendment.