Εμφάνιση απλής εγγραφής

dc.creatorEl Azhari N., Dermou E., Barnard R.L., Storck V., Tourna M., Beguet J., Karas P.A., Lucini L., Rouard N., Botteri L., Ferrari F., Trevisan M., Karpouzas D.G., Martin-Laurent F.en
dc.date.accessioned2023-01-31T07:37:09Z
dc.date.available2023-01-31T07:37:09Z
dc.date.issued2018
dc.identifier10.1016/j.scitotenv.2018.05.088
dc.identifier.issn00489697
dc.identifier.urihttp://hdl.handle.net/11615/71297
dc.description.abstractTebuconazole (TBZ) is a widely used triazole fungicide at EU level on cereals and vines. It is relatively persistent in soil where it is transformed to various transformation products (TPs) which might be environmentally relevant. We assessed the dissipation of TBZ in soil under contrasting incubation conditions (standard vs winter simulated) that are relevant to its application scheme, determined its transformation pathway using advanced analytical tools and 14 C-labeled TBZ and assessed its soil microbial toxicity. Mineralization of 14 C-triazole-ring-labeled TBZ was negligible but up to 11% of 14 C-penyl-ring-labeled TBZ evolved as 14 CO 2 within 150 days of incubation. TBZ persistence increased at higher dose rates (×10 compared to the recommended agronomical dose ×1) and under winter simulated conditions compared to standard incubation conditions (at ×1 dose rate DT 50 of 202 and 88 days, respectively). Non-target suspect screening enabled the detection of 22 TPs of TBZ, among which 17 were unknown. Mass spectrometry analysis led to the identification of 1-(4-chlorophenyl) ethanone, a novel TP of TBZ, the formation of which and decay in soil was determined by gas chromatography mass spectrometry. Three hypothetical transformation pathways of TBZ, all converging to 1H-1,2,4-triazole are proposed based on suspect screening. The ecotoxicological effect of TBZ and of its TPs was assessed by measuring by qPCR the abundance of the total bacteria and the relative abundance of 11 prokaryotic taxa and 4 functional groups. A transient impact of TBZ on the relative abundance of all prokaryotic taxa (except α-proteobacteria and Bacteroidetes) and one functional microbial group (pcaH-carrying microorganisms) was observed. However the direction of the effect (positive or negative) varied, and in certain cases, depended on the incubation conditions. Proteobacteria was the most responsive phylum to TBZ with recovery observed 20 days after treatment. The ecotoxicological effects on the soil microorganisms were not correlated with 1-(4-chlorophenyl) ethanone. © 2018 Elsevier B.V.en
dc.language.isoenen
dc.sourceScience of the Total Environmenten
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85047058450&doi=10.1016%2fj.scitotenv.2018.05.088&partnerID=40&md5=5765273a205a3baa70709304fa64f899
dc.subjectEnergy dissipationen
dc.subjectGas chromatographyen
dc.subjectMass spectrometryen
dc.subjectMicroorganismsen
dc.subjectPolymerase chain reactionen
dc.subjectToxicityen
dc.subjectEco-toxicologyen
dc.subjectEcotoxicological effectsen
dc.subjectGas chromatography-mass spectrometryen
dc.subjectMass spectrometry analysisen
dc.subjectSoil micro-organismsen
dc.subjectTebuconazoleen
dc.subjectTransformation pathwaysen
dc.subjectTransformation productsen
dc.subjectSoilsen
dc.subject1 (4 chlorophenyl) 4 methyl 3 (1,2,4 triazol 1 ylmethyl)pentan 3 olen
dc.subject1 (4 chlorophenyl) 4,4 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentan 3 olen
dc.subject1 (4 chlorophenyl) ethanoneen
dc.subject1 (4 clorophenyl) 3 (1,2,4 triazol 1 ylmethyl)pentan 3 olen
dc.subject1h 1,2,4 triazoleen
dc.subject2 (1,2,4 triazol 1 yl)acetic aciden
dc.subject2 (1,2,4 triazol 1 yl)ethane 1,1 diolen
dc.subject2 hydroxy 3,3 dimethyl 2 (1,2,4 triazol 1 ylmethyl)butanoic aciden
dc.subject2,2 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentan 3 olen
dc.subject3 hydroxy 4,4 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentanoic aciden
dc.subject3,3 dimethyl 1 (1,2,4 triazol 1 yl)butan 2 oneen
dc.subject4 hydroxy 5,5 dimethyl 4 (1,2,4 triazol 1 ylmethyl)hexanoic aciden
dc.subject4 [3 hydroxy 4,4 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentyl]benzene 1,2 diolen
dc.subject4 [3 hydroxy 4,4 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentyl]phenolen
dc.subject5 (4 chlorophenyl) 2,2 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentane 1,3 diolen
dc.subject5 (4 chlorophenyl) 3 hydroxy 2 methyl 3 (1,2,4 triazol 1 ylmethyl)pentanoic aciden
dc.subject5 (4 chlorophenyl) 3 hydroxy 2,2 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentanoic aciden
dc.subject5 (4 chlorophenyl) 3 hydroxy 3 (1,2,4 triazol 1 ylmethyl)pentanoic aciden
dc.subject5 hydroxy 6,6 dimethyl 5 (1,2,4 triazol 1 ylmethyl)heptanoic aciden
dc.subject5 tert butyl 5 (1,2,4 triazol 1 ylmethyl) tetrahydrofuran 2 oneen
dc.subject8 hydroxy 9,9 dimethyl 2 oxo 8 (1,2,4 triazol 1 ylmethyl)dec 4 enoic aciden
dc.subjectbenzene derivativeen
dc.subjectcarbonen
dc.subjectcarbon 14en
dc.subjectcarbon dioxideen
dc.subjectnitrogenen
dc.subjectsulfuren
dc.subjecttebuconazoleen
dc.subjecttriazole derivativeen
dc.subjectunclassified drugen
dc.subjectunindexed drugen
dc.subjectfungicideen
dc.subjecttebuconazoleen
dc.subjecttriazole derivativeen
dc.subjectdissipationen
dc.subjectecotoxicologyen
dc.subjectlaboratory methoden
dc.subjectmass spectrometryen
dc.subjectpolymerase chain reactionen
dc.subjectrelative abundanceen
dc.subjectsoil biotaen
dc.subjecttebuconazoleen
dc.subjecttransformationen
dc.subjectwinteren
dc.subjectArticleen
dc.subjectbacteriumen
dc.subjectbiogeochemical cyclingen
dc.subjectbiotransformationen
dc.subjectcarbon cyclingen
dc.subjectchemical reaction kineticsen
dc.subjectchemical structureen
dc.subjectcontrolled studyen
dc.subjectecotoxicityen
dc.subjectincubation timeen
dc.subjectisotope labelingen
dc.subjectlaboratoryen
dc.subjectliquid chromatography-mass spectrometryen
dc.subjectmass fragmentographyen
dc.subjectmass spectrometryen
dc.subjectmineralizationen
dc.subjectnitrogen cyclingen
dc.subjectnonhumanen
dc.subjectpolymerase chain reactionen
dc.subjectpopulation abundanceen
dc.subjectpriority journalen
dc.subjectprokaryoteen
dc.subjectProteobacteriaen
dc.subjectquantitative analysisen
dc.subjectrespirometryen
dc.subjectsimulationen
dc.subjectsoil and soil related phenomenaen
dc.subjectsoil dissipationen
dc.subjectsoil microfloraen
dc.subjectsulfur cyclingen
dc.subjecttime of flight mass spectrometryen
dc.subjectwinteren
dc.subjectanalysisen
dc.subjectmicrobiologyen
dc.subjectseasonen
dc.subjectsoilen
dc.subjectsoil pollutanten
dc.subjecttoxicityen
dc.subjectAlphaproteobacteriaen
dc.subjectBacteria (microorganisms)en
dc.subjectBacteroidetesen
dc.subjectProkaryotaen
dc.subjectProteobacteriaen
dc.subjectFungicides, Industrialen
dc.subjectSeasonsen
dc.subjectSoilen
dc.subjectSoil Microbiologyen
dc.subjectSoil Pollutantsen
dc.subjectTriazolesen
dc.subjectElsevier B.V.en
dc.titleThe dissipation and microbial ecotoxicity of tebuconazole and its transformation products in soil under standard laboratory and simulated winter conditionsen
dc.typejournalArticleen


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