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1.
Environ Toxicol ; 28(12): 689-99, 2013 Dec.
Article in English | MEDLINE | ID: mdl-22012874

ABSTRACT

This study investigated the effects on the physiology of Pacific oyster, Crassostrea gigas, of a mixture of pesticides containing 0.8 µg L(-1) alachlor, 0.6 µg L(-1) metolachlor, 0.7 µg L(-1) atrazine, 0.6 µg L(-1) terbuthylazine, 0.5 µg L(-1) diuron, 0.6 µg L(-1) fosetyl aluminum, 0.05 µg L(-1) carbaryl, and 0.7 µg L(-1) glyphosate for a total concentration of 4.55 µg L(-1) . The total nominal concentration of pesticides mixture corresponds to the pesticide concentrations in the shellfish culture area of the Marennes-Oleron basin. Two varieties of C. gigas were selected on the foreshore, based on their characteristics in terms of resistance to summer mortality, to assess the effects of the pesticide mixture after 7 days of exposure under controlled conditions. The early effects of the mixture were assessed using enzyme biomarkers of nitrogen metabolism (GS, glutamine synthetase), detoxification metabolism (GST, glutathione S-transferase), and oxidative stress (CAT, catalase). Sublethal effects on hemocyte parameters (phagocytosis and esterase activity) and DNA damages (DNA adducts) were also measured. Changes in metabolic activities were characterized by increases in GS, GST, and CAT levels on the first day of exposure for the "resistant" oysters and after 3-7 days of exposure for the "susceptible" oysters. The formation of DNA adducts was detected after 7 days of exposure. The percentage of hemocyte esterase-positive cells was reduced in the resistant oysters, as was the hemocyte phagocytic capacity in both oyster varieties after 7 days of exposure to the pesticide mixture. This study highlights the need to consider the low doses and the mixture of pesticides to evaluate the effects of these molecules on organisms.


Subject(s)
Crassostrea/drug effects , Pesticides/toxicity , Water Pollutants, Chemical/toxicity , Animals , Catalase/metabolism , Crassostrea/immunology , Crassostrea/metabolism , DNA Damage , Glutamate-Ammonia Ligase/metabolism , Glutathione Transferase/metabolism , Hemocytes/drug effects , Hemocytes/immunology , Hemocytes/physiology , Phagocytosis
2.
Environ Sci Technol ; 46(4): 2375-82, 2012 Feb 21.
Article in English | MEDLINE | ID: mdl-22236067

ABSTRACT

Fecal contaminations of inland and coastal waters induce risks to human health and economic losses. To improve water management, specific markers have been developed to differentiate between sources of contamination. This study investigates the relative decay of fecal indicator bacteria (FIB, Escherichia coli and enterococci) and six human-associated markers (two bacterial markers: Bacteroidales HF183 (HF183) and Bifidobacterium adolescentis (BifAd); one viral marker: genogroup II F-specific RNA bacteriophages (FRNAPH II); three chemical markers: caffeine and two fecal stanol ratios) in freshwater and seawater microcosms seeded with human wastewater. These experiments were performed in darkness, at 20 °C and under aerobic conditions. The modeling of the decay curves allows us (i) to compare FIB and markers and (ii) to classify markers according to their persistence in seawater (FRNAPH II < HF183, stanol ratios < BifAd, caffeine) and in freshwater (HF183, stanol ratios < FRNAPH II < BifAd < caffeine). Although those results depend on the experimental conditions, this study represents a necessary step to develop and validate an interdisciplinary toolbox for the investigation of the sources of fecal contaminations.


Subject(s)
Bacteria/isolation & purification , Feces/microbiology , Fresh Water/microbiology , Seawater/microbiology , Sewage/microbiology , Water Pollutants/analysis , Bacterial Load , Biomarkers/analysis , Caffeine/analysis , Environmental Monitoring , Humans , Sterols/analysis , Water Microbiology
3.
Water Res ; 44(16): 4812-24, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20709349

ABSTRACT

The microbiological quality of coastal or river waters can be affected by faecal pollution from human or animal sources. An efficient MST (Microbial Source Tracking) toolbox consisting of several host-specific markers would therefore be valuable for identifying the origin of the faecal pollution in the environment and thus for effective resource management and remediation. In this multidisciplinary study, after having tested some MST markers on faecal samples, we compared a selection of 17 parameters corresponding to chemical (steroid ratios, caffeine, and synthetic compounds), bacterial (host-specific Bacteroidales, Lactobacillus amylovorus and Bifidobacterium adolescentis) and viral (genotypes I-IV of F-specific bacteriophages, FRNAPH) markers on environmental water samples (n = 33; wastewater, runoff and river waters) with variable Escherichia coli concentrations. Eleven microbial and chemical parameters were finally chosen for our MST toolbox, based on their specificity for particular pollution sources represented by our samples and their detection in river waters impacted by human or animal pollution; these were: the human-specific chemical compounds caffeine, TCEP (tri(2-chloroethyl)phosphate) and benzophenone; the ratios of sitostanol/coprostanol and coprostanol/(coprostanol+24-ethylcopstanol); real-time PCR (Polymerase Chain Reaction) human-specific (HF183 and B. adolescentis), pig-specific (Pig-2-Bac and L. amylovorus) and ruminant-specific (Rum-2-Bac) markers; and human FRNAPH genogroup II.


Subject(s)
Bathing Beaches , Feces/microbiology , Rivers/chemistry , Rivers/microbiology , Shellfish , Water Microbiology , Water Pollution/analysis , Animals , Base Sequence , Bifidobacterium/growth & development , Bifidobacterium/isolation & purification , Caffeine/analysis , Escherichia coli/growth & development , Escherichia coli/isolation & purification , France , Humans , Lactobacillus/growth & development , Lactobacillus/isolation & purification , Polymerase Chain Reaction , RNA Phages/growth & development , RNA Phages/isolation & purification , Steroids/analysis , Viruses/growth & development , Viruses/isolation & purification , Water Pollution, Chemical/analysis
4.
J Chromatogr A ; 1108(1): 129-35, 2006 Mar 03.
Article in English | MEDLINE | ID: mdl-16443233

ABSTRACT

An analytical method has been developed for the determination of residues of ethephon (2-chloroethyl phosphonic acid) in drinking and surface water. The procedure is based on de-ionisation with an anion/cation-exchange resin, solid phase extraction by means of anion-exchange polystyrene-divinylbenzene extraction disks, elution with a mixture of methanol and 10 M hydrochloric acid (98/2, v/v), redisolution into acetonitrile after evaporation and silylation with N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA). Quantification is performed by gas chromatography with ion-trap cubic mass spectrometric detection in the electron impact mode (GC-EI-MS3). Method validation was conducted using samples of mineral, tap, and river water that were fortified with ethephon at concentration levels ranging from 0.1 to 1.0 microg/L. The mean recovery from all the fortified samples (n = 36) amounted to 88% with a relative standard deviation of 17%. The method, therefore, was shown to allow accurate determination of ethephon residues in drinking and surface water with a limit of quantification of 0.1 microg/L.


Subject(s)
Gas Chromatography-Mass Spectrometry/methods , Organophosphorus Compounds/analysis , Water Pollutants, Chemical/analysis , Acetamides , Chromatography, Ion Exchange , Fluoroacetates , Organosilicon Compounds/chemistry , Trifluoroacetic Acid/chemistry
5.
J Agric Food Chem ; 49(5): 2152-8, 2001 May.
Article in English | MEDLINE | ID: mdl-11368570

ABSTRACT

The determination of dithiocarbamates in plant matrixes is generally carried out by spectrophotometric (European Norm EN 12396-1, 1996) or gas chromatography headspace (European Norm EN 12396-2, 1999) methods. However, the former method presents a risk of carbon disulfide loss during hydrolysis and distillation and its sensitivity is low, whereas the latter method is time-consuming. In comparison to these European methods and in compliance with norm V03-110, we have developed an automated gas chromatography headspace method. This method offers a good level of accuracy and precision and is specific to the compound determined (CS(2)). The limit of detection is below 0.020 mg/kg and the limit of quantification is below 0.050 mg/kg. Moreover, the recovery rates are between 85 and 103% with RSD less than 20%. The automated headspace method has several advantages when compared to the spectrophotometric and manual headspace methods, including the reduction of reagents employed for extraction and a greater number of analyses achievable per day than the other methods (approximately 40 samples of food).


Subject(s)
Chromatography, Gas/methods , Plants/chemistry , Thiocarbamates/analysis , Reproducibility of Results , Sensitivity and Specificity
6.
J Agric Food Chem ; 48(11): 5184-9, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11087456

ABSTRACT

An analytical method for the determination of glufosinate ammonium and its principal metabolites, AE F064619 and AE F061517, in water of two different hardnesses (5 and 30 DH, French hardness) has been developed and validated. Samples were spiked at different levels (0. 05 and 0.5 microgram/L) and were purified by column chromatography on ion-exchange resins. After derivatization with glacial acetic acid and trimethylarthoacetate mixture, the derivatives were quantified by using capillary gas chromatography with an ion-trap tandem mass spectrometric detector. Analytical conditions for MS/MS detection were optimized, and the quantification was carried out on the areas of the most representative ions. The limit of quantification was validated at 0.05 microgram/L for each compound. The mean recovery value and the relative standard deviation (n = 20) were 92.0% and 17. 8% for glufosinate ammonium, 90.2% and 15.8% for AE F064619, and 89. 7% and 12.7% for AE F061517.


Subject(s)
Acetates/analysis , Aminobutyrates/analysis , Drug Residues/analysis , Herbicides/analysis , Organophosphonates/analysis , Propionates/analysis , Water/analysis , France , Gas Chromatography-Mass Spectrometry/methods , Indicators and Reagents , Sensitivity and Specificity
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