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Environmental Monitoring and Assessment Jun 2017The state of Sinaloa in Mexico is an industrialized agricultural region with a documented pesticide usage of 700 t year; which at least 17 of the pesticides are...
The state of Sinaloa in Mexico is an industrialized agricultural region with a documented pesticide usage of 700 t year; which at least 17 of the pesticides are classified as moderately to highly toxic. Pollutants in the water column of rivers and drains are of great concern because the water flows into coastal lagoons and nearshore waters and thereby affects aquatic organisms. This study was done in four municipalities in the state of Sinaloa that produce food intensively. To investigate the link between pollution in the lagoons and their proximity to agricultural sites, water was sampled in three coastal lagoons and in the rivers and drains that flow into them. Seawater from the Gulf of California, 10 km from the coast, was also analyzed. Concentrations of nutrients, organochlorines, and organophosphorus pesticides were determined. Nutrient determination showed an unhealthy environment with N/P ratios of <16, thus favoring nitrogen-fixing cyanobacteria. The organochlorine pesticides showed a clear accumulation in the coastal lagoons from the drains and rivers, with ΣHCH showing the highest concentrations. In the southern part of the region studied, pollution of the coastal lagoon of Pabellones could be traced mainly to the drains from the agricultural sites. Accumulation of OC pesticides was also observed in the Gulf of California. Tests for 22 organophosphates revealed only five (diazinon, disulfoton, methyl parathion, chlorpyrifos, and mevinphos); diazinon was detected at all the sites, although methyl parathion was present at some sites at concentrations one order of magnitude higher than diazinon.
Topics: Agriculture; Agrochemicals; California; Chlorpyrifos; Diazinon; Environmental Monitoring; Hydrocarbons, Chlorinated; Mexico; Pesticides; Rivers; Seawater; Water Pollutants, Chemical; Water Pollution, Chemical
PubMed: 28510105
DOI: 10.1007/s10661-017-5981-8 -
Food Chemistry Nov 2019An analytical method involving QuEChERS (quick, easy, cheap, effective, rugged, and safe) sample preparation, followed by LC-MS/MS and GC-MS/MS was developed and...
An analytical method involving QuEChERS (quick, easy, cheap, effective, rugged, and safe) sample preparation, followed by LC-MS/MS and GC-MS/MS was developed and validated for the determination of 60 pesticides in eggs. Recoveries of 70-120% were achieved for selected pesticides and relative standard deviations <20% were obtained for most analytes at three concentrations. The limit of quantification was <10 µg kg for 83% of the total pesticides. This method was used to analyze 58 egg samples and the residues of seven pesticides (disulfoton, fipronil sulfone, cyromazine, o,p-DDT, p,p-DDD, p,p-DDT, and permethrin) were quantified in 16 egg samples at levels of 5-10 µg kg, which was below the corresponding the maximum residue levels, as established by Korean Ministry of Food and Drug Safety. We demonstrated that LC-MS/MS and GC-MS/MS in combination with QuEChERS can be used to routinely monitor multiple pesticide residues in egg samples.
Topics: Animals; Chickens; Chromatography, High Pressure Liquid; Disulfoton; Eggs; Female; Gas Chromatography-Mass Spectrometry; Limit of Detection; Pesticide Residues; Pyrazoles; Reproducibility of Results; Tandem Mass Spectrometry
PubMed: 31260955
DOI: 10.1016/j.foodchem.2019.125050 -
Chemosphere Aug 2014The interaction mechanisms of catalase (CAT) with pesticides (including organophosphates: disulfoton, isofenphos-methyl, malathion, isocarbophos, dimethoate, dipterex,...
The interaction mechanisms of catalase (CAT) with pesticides (including organophosphates: disulfoton, isofenphos-methyl, malathion, isocarbophos, dimethoate, dipterex, methamidophos and acephate; carbamates: carbaryl and methomyl; pyrethroids: fenvalerate and deltamethrin) were first investigated by flow injection (FI) chemiluminescence (CL) analysis and molecular docking. By homemade FI-CL model of lg[(I0-I)/I]=lgK+nlg[D], it was found that the binding processes of pesticides to CAT were spontaneous with the apparent binding constants K of 10(3)-10(5) L mol(-1) and the numbers of binding sites about 1.0. The binding abilities of pesticides to CAT followed the order: fenvalerate>deltamethrin>disulfoton>isofenphos-methyl>carbaryl>malathion>isocarbophos>dimethoate>dipterex>acephate>methomyl>methamidophos, which was generally similar to the order of determination sensitivity of pesticides. The thermodynamic parameters revealed that CAT bound with hydrophobic pesticides by hydrophobic interaction force, and with hydrophilic pesticides by hydrogen bond and van der Waals force. The pesticides to CAT molecular docking study showed that pesticides could enter into the cavity locating among the four subdomains of CAT, giving the specific amino acid residues and hydrogen bonds involved in CAT-pesticides interaction. It was also found that the lgK values of pesticides to CAT increased regularly with increasing lgP, Mr, MR and MV, suggesting that the hydrophobicity and steric property of pesticide played essential roles in its binding to CAT.
Topics: Animals; Catalase; Cattle; Flow Injection Analysis; Luminescence; Luminescent Measurements; Molecular Docking Simulation; Pesticides; Protein Binding; Thermodynamics
PubMed: 24875908
DOI: 10.1016/j.chemosphere.2014.02.075 -
Royal Society Open Science Jul 2018This study was performed to determine the storage stability of organophosphorus pesticide residues in high oil content commodity matrices, peanut and soya bean. The...
This study was performed to determine the storage stability of organophosphorus pesticide residues in high oil content commodity matrices, peanut and soya bean. The storage conditions included different types of solvents (ethyl acetate, acetone and hexane) and corresponding extracted matrix solutions, light and temperature. It was found that three pesticides degraded quickly especially in ethyl acetate solvent. They decreased greater than 30% when stored for 3 days at -20°C in ethyl acetate; the results showed that the stability could be improved in the extracted matrix solutions. Light had a slight effect for stability of phorate and fenthion, while it played an important effect for disulfoton with the exception of ethyl acetate as solvent. Even at -20°C, exposure to solvents or extracted matrix solution resulted in 40.67, 96.33 and 35.07% loss of phorate, disulfoton and fenthion. Hence, it could be assumed that these three residues could be more stable at lower temperature, in the dark and in acetone or hexane extracted peanut and soya bean solutions.
PubMed: 30109115
DOI: 10.1098/rsos.180757 -
Journal of Environmental Science and... 2015The objective of this study was to determine the levels of pesticides in the fish Prochilodus costatus caught in São Francisco River, one of most important rivers in...
The objective of this study was to determine the levels of pesticides in the fish Prochilodus costatus caught in São Francisco River, one of most important rivers in Brazil. Thirty-six fish were captured in three different areas, and samples of the dorsal muscle and pooled viscera were collected for toxicological analysis. We evaluated the presence of 150 different classes of insecticides, fungicides, herbicides and acaricides by multiresidue analysis technique using liquid chromatography-tandem mass spectrometry (LC-MS/MS), with the limit of detection of 5 ppb. In this study, organophosphorus and carbamate pesticides were detected at the highest levels in the caught fish. Among the 41 organophosphorus pesticides surveyed, nine types were detected (chlorpyrifos, diazinon, dichlorvos, disulfoton, ethion, etrimfos, phosalone, phosmet and pyrazophos) in the muscle, viscera pool, or both in 22 (61.1%) fish. Sampled tissues of 20 (55.6%) fish exhibited at least one of the eight evaluated carbamate pesticides and their metabolites: aldicarb, aldicarb sulfoxide, carbaryl, carbofuran, carbosulfan, furathiocarb, methomyl and propoxur. Fungicides (carbendazim, benalaxyl, kresoxim-methyl, trifloxystrobin, pyraclostrobin and its metabolite BF 500 pyraclostrobin), herbicides (pyridate and fluasifop p-butyl), acaricide (propargite) and pyrethroid (flumethrin) were also detected. In conclusion, P. costatus fish caught in the São Francisco River contained residues of 17 different pesticides, in both muscles and the viscera pool, indicating heavy environmental contamination by pesticides in the study area.
Topics: Animals; Brazil; Characiformes; Environmental Monitoring; Muscle, Skeletal; Pesticide Residues; Pesticides; Rivers; Water Pollutants, Chemical
PubMed: 25844860
DOI: 10.1080/03601234.2015.1011946 -
Macromolecular Rapid Communications Jun 2018The threat of chemical warfare agents (CWA) compels research into novel self-decontaminating materials (SDM) for the continued safety of first-responders, civilians, and...
The threat of chemical warfare agents (CWA) compels research into novel self-decontaminating materials (SDM) for the continued safety of first-responders, civilians, and active service personnel. The capacity to actively detoxify, as opposed to merely sequester, offending agents under typical environmental conditions defines the added value of SDMs in comparison to traditional adsorptive materials. Porous polymers, synthesized via the high internal phase emulsion (HIPE) templating, provide a facile fabrication method for materials with permeable open cellular structures that may serve in air filtration applications. PolyHIPEs comprising polydicyclopentadiene (polyDCPD) networks form stable hydroperoxide species following activation in air under ambient conditions. The hydroperoxide-containing polyDCPD materials react quickly with CWA simulants, Demeton-S and 2-chloroethyl ethyl sulfide, forming oxidation products as confirmed via gas chromatography mass spectrometry. The simplicity of the detoxification chemistry paired with the porous foam form factor presents an exciting opportunity for the development of self-decontaminating filter media.
Topics: Chemical Warfare Agents; Chromatography, Liquid; Decontamination; Disulfoton; Emulsions; Hydrogen Peroxide; Indenes; Mass Spectrometry; Mustard Gas; Oxidation-Reduction; Polymers; Porosity; Styrenes; Time Factors
PubMed: 29786164
DOI: 10.1002/marc.201800194 -
Food Chemistry Dec 2017Due the negative effects of pesticides on environment and human health, more efficient and environmentally friendly methods are needed. In this sense, a simple, fast,...
Due the negative effects of pesticides on environment and human health, more efficient and environmentally friendly methods are needed. In this sense, a simple, fast, free from memory effects and economical direct-immersion single drop micro-extraction (SDME) method and GC-MS for multi-class pesticides determination in mango samples was developed. Sample pre-treatment using ultrasound-assisted solvent extraction and factors affecting the SDME procedure (extractant solvent, drop volume, stirring rate, ionic strength, time, pH and temperature) were optimized using factorial experimental design. This method presented high sensitive (LOD: 0.14-169.20μgkg), acceptable precision (RSD: 0.7-19.1%), satisfactory recovery (69-119%) and high enrichment factors (20-722). Several obtained LOQs are below the MRLs established by the European Commission; therefore, the method could be applied for pesticides determination in routing analysis and custom laboratories. Moreover, this method has shown to be suitable for determination of some of the studied pesticides in lime, melon, papaya, banana, tomato, and lettuce.
Topics: Gas Chromatography-Mass Spectrometry; Lactuca; Mangifera; Pesticides
PubMed: 28764000
DOI: 10.1016/j.foodchem.2017.05.030 -
Bulletin of Environmental Contamination... Oct 2015A simple, rapid and sensitive spectrofluorimetric method was developed for the determination of di-syston, ethion and phorate in environmental water samples. The...
A simple, rapid and sensitive spectrofluorimetric method was developed for the determination of di-syston, ethion and phorate in environmental water samples. The procedure is based on the oxidation of these pesticides with cerium (IV) to produce cerium (III), and its fluorescence was monitored at 368 ± 3 nm after excitation at 257 ± 3 nm. The variables effecting oxidation of each pesticide were studied and optimized. Under the experimental conditions used, the calibration graphs were linear over the range 0.2-15, 0.1-13, 0.1-13 ng mL(-1) for di-syston, ethion and phorate, respectively. The limit of detection and quantification were in the range 0.034-0.096 and 0.112-0.316 ng mL(-1), respectively. Intra- and inter-day assay precisions, expressed as the relative standard deviation (RSD), were lower than 5.2 % and 6.7 %, respectively. Good recoveries in the range 86 %-108 % were obtained for spiked water samples. The proposed method was applied to the determination of studied pesticides in environmental water samples.
Topics: Disulfoton; Environmental Monitoring; Insecticides; Organothiophosphorus Compounds; Phorate; Spectrometry, Fluorescence; Water Quality
PubMed: 26210825
DOI: 10.1007/s00128-015-1612-7