Morphological variations and demographic responses of the Mediterranean pond turtle Mauremys leprosa to heterogeneous aquatic habitats.

Human activities affect terrestrial and aquatic habitats leading to changes at both individual and population levels in wild animal species. In this study, we investigated the phenotype and demographics of the Mediterranean pond turtle Mauremys leprosa (Schweigger, 1812) in contrasted environments of Southern France: two peri-urban rivers receiving effluents from wastewater treatment plants (WWTP), and another one without sewage treatment plant. Our findings revealed the presence of pesticides and pharmaceuticals in the three rivers of investigation, the highest diversities and concentrations of pollutants being found in the river subsections impacted by WWTP effluents. Principal component analysis and hierarchical clustering identified three levels of habitat quality, with different pollutant concentrations, thermal conditions, nutrient, and organic matter levels. The highest turtle densities, growth rates, and body sizes were estimated in the most disturbed habitats, suggesting potential adult benefits derived from harsh environmental conditions induced by pollution and eutrophication. Conversely, juveniles were the most abundant in the least polluted habitats, suggesting adverse effects of pollution on juvenile survival or adult reproduction. This study suggests that turtles living in polluted habitats may benefit from enhanced growth and body size, at the expense of reproductive success.

Thiophenium Salts as New Oxidant for Redox Polymerization under Mild- and Low-Toxicity Conditions.

In mild conditions (under air, room temperature, no monomer purification and without any energy activation), redox free radical polymerization (RFRP) is considered as one of the most effective methods to polymerize (meth)acrylate monomers. In the past several years, there has been a growing interest in research on the development of new redox initiating systems (RISs), thanks mainly to the evolution of toxicity labeling and the stability issue of the current RIS based on peroxide and aromatic amine. In this study, a new, low-toxicity RIS based on thiophenium salt as the oxidant species is presented with various reductive species. The reactivity and the stability of the proposed RISs are investigated and the synthesis of new thiophenium salts reported.

Electron ionization mass spectrometric fragmentation and multiple reaction monitoring quantification of ferulic and p-coumaric acid trimethylsilyl derivatives in deposited atmospheric particles.

RATIONALE: Ferulic and p-coumaric acids are important biological and structural components of plant cell walls and possess antioxidant and antimicrobial properties. These phenolic acids are widespread in environmental samples. However, when they are present at very low concentrations or in very complex lipid extracts, their identification and quantification can be challenging. METHODS: The electron ionization mass spectrometry (EI-MS) fragmentation pathways of ferulic and p-coumaric acid trimethylsilyl (TMS) derivatives were investigated. These pathways were deduced by (i) low-energy collision-induced dissociation (CID) gas chromatography (GC)/EI-MS/MS, (ii) accurate mass measurement, and (iii) 13 C labelling. These compounds were then characterized and quantified in multiple reaction monitoring (MRM) mode in total lipid extracts of deposited atmospheric particles using highly specific transitions based on the main fragmentation pathways elucidated. RESULTS: Low-energy CID-MS/MS analyses, accurate mass measurement and 13 C labelling enabled us to elucidate EI-MS fragmentations of ferulic and p-coumaric acid TMS derivatives. Some specific fragmentations proved useful for subsequent characterization and quantification of these compounds. As an application of some of the described fragmentations, trace amounts of these phenolic acids were characterized and quantified in MRM mode in wet- and dry-deposited atmospheric particles containing low proportions of organic matter. CONCLUSIONS: EI-MS fragmentations of ferulic and p-coumaric acid TMS derivatives exhibit specific fragment ions that can be very useful for the quantification of trace amounts of both phenolic acids in environmental samples.

Microplastic fluxes in a large and a small Mediterranean river catchments: The Têt and the Rhône, Northwestern Mediterranean Sea.

This paper aims at quantifying current riverine fluxes of microplastics (MPs) in two Mediterranean river catchments, a large one and a small one, namely the Rhône and the Têt, which are discharging to the Gulf of Lion in the Northwestern Mediterranean Sea. MP fluxes change markedly through time and space in both river systems. However, no clear relationships between MP concentrations and hydroclimatic conditions have been observed. In the Rhône River a non-linear dilution pattern of MPs in total suspended matter (TSM) during flood conditions could be observed. Although dilution is important, samples during floods exert a strong control on average MP fluxes. Compared to the Rhône River, average MP concentrations in the Têt River were throughout greater and more variable in shape and polymer composition. However, as the study year was exceptionally dry, the average specific MP flux, 76 g km-2 y-1, is only slightly larger than the non-flooding value of the Rhône River. We further monitored MP concentrations in shoreline sediments at the mouth of the Têt River to test whether these sediments can represent MP transport in the river. Besides fibers, which probably are easily washed out and transported offshore, MP concentrations and compositions are in agreement with MP loads upstream the river. We also examined the potential role of atmospheric deposition as a source of MP to the Têt River. The average atmospheric MP deposition of 6 kg km-2 y-1 exceeds by far the river average specific MP flux. Moreover, all MPs in atmospheric deposits were fibers, which in terms of mass are of minor importance in the bulk river fluxes. Atmospheric MP deposits may either have been overestimated and/or may be removed from surface waters by efficient removal processes (such as waste water treatment plants).

EIMS Fragmentation and MRM quantification of autoxidation products of α- and ß-amyrins in natural samples.

RATIONALE: Riverine particulate organic matter is generally considered to be refractory with respect to further decomposition in the ocean. In order to check the validity of this paradigm, there is a real need for tracers sufficiently stable and specific to monitor the degradation of terrestrial higher plant material in the environment. 3ß-hydroxy-urs-12-en-11-one and 3ß-hydroxy-olean-12-en-11-one (autoxidation products of α- and ß-amyrin) were previously proposed for such use. METHODS: EIMS fragmentation pathways of 3ß-hydroxy-urs-12-en-11-one and 3ß-hydroxy-olean-12-en-11-one TMS derivatives were investigated. These pathways were deduced by: (i) low energy CID-GC/MS/MS, (ii) accurate mass measurement and (iii) deuterium labelling. Quantification of these compounds in total lipid extracts of natural samples was then carried out in MRM mode. RESULTS: CID-MS/MS analyses, accurate mass measurement and deuterium labelling experiments allowed us to elucidate EIMS fragmentations of 3ß-hydroxy-urs-12-en-11-one and 3ß-hydroxy-olean-12-en-11-one TMS derivatives. Some specific fragmentation pathways, useful in addition to chromatographic retention times for further characterization, could be selected. As an application of some of the described fragmentations, TMS derivatives of these oxidation products were characterized and quantified in MRM mode in different natural samples. CONCLUSIONS: EIMS fragmentations of 3ß-hydroxy-urs-12-en-11-one and 3ß-hydroxy-olean-12-en-11-one TMS derivatives exhibit specific fragment ions, which appear to be very useful for the quantification of these oxidation products in natural samples (riverine particulate matter, wet and dry deposited atmospheric particles).

Variability of Solar Radiation and CDOM in Surface Coastal Waters of the Northwestern Mediterranean Sea.

Atmospheric and in-water solar radiation, including UVR-B, UVR-A and PAR, as well as chromophoric dissolved organic matter absorption [aCDOM (λ)] in surface waters were monthly measured from November 2007 to December 2008 at a coastal station in the Northwestern Mediterranean Sea (Bay of Marseilles, France). Our results showed that the UVR-B/UVR-A ratio followed the same trend in the atmosphere and at 2 m depth in the water (P < 0.0001) with an increase (eight-fold higher) during summer. The low diffuse attenuation coefficients for downward irradiance [Kd (λ)] of UVR-B, UVR-A and PAR indicated that the waters were highly transparent throughout the year. The relationships between aCDOM (λ) and Kd (λ) in this oligotrophic system suggested that CDOM contributed to UVR attenuation in the UVA domain, but also played a significant role in PAR attenuation. Mean UV doses received in the mixed layer depth were higher by a factor 1.4-33 relative to doses received at fixed depths (5 and 10 m) in summer (stratified period), while the inverse pattern was found in winter (mixing period). This shows the importance of taking into account the vertical mixing in the evaluation of UVR effects on marine organisms.

Determination of low molecular weight dicarboxylic and ketocarboxylic acids in seawater samples.

We report a new method developed for the isolation and determination of low molecular weight dicarboxylic acids and related polar compounds (C2-C9) from seawater samples. The seawater sample was first acidified and then passed through an activated charcoal column to adsorb the dicarboxylic acids. They are then desorbed with NH4OH/methanol/water mixture and derivatized with BF3/1-butanol to dibutyl esters, which are determined using a capillary GC/FID. We tested different pH (0.5, 1, 1.5) and different amounts of charcoal (100, 200, 300, 500 mg) to maximize the recovery of dicarboxylic acids. Using 300 mg of activated charcoal for 100 mL of sodium chloride solution acidified at pH 1, the recoveries for C2, C3, C4, C5, C6, C7, C8, and C9 were 61, 49, 96, 84, 77, 67, 57, and 53%, respectively. We applied this method to real seawater samples collected from the northwestern Mediterranean Sea. Here, we report, for the first time, concentrations of a homologous series of C2-C9 dicarboxylic acids as well as ketocarboxylic acids including glyoxylic and 4-oxobutanoic acids in surface water and deep seawater samples, with glyoxylic acid being the dominant species (8-40 microg L(-1)). This method allows the detection of dicarbonyls such as glyoxal in the samples although its quantification is not possible.