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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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The dissipation and microbial ecotoxicity of tebuconazole and its transformation products in soil under standard laboratory and simulated winter conditions

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Author
El 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.
Date
2018
Language
en
DOI
10.1016/j.scitotenv.2018.05.088
Keyword
Energy dissipation
Gas chromatography
Mass spectrometry
Microorganisms
Polymerase chain reaction
Toxicity
Eco-toxicology
Ecotoxicological effects
Gas chromatography-mass spectrometry
Mass spectrometry analysis
Soil micro-organisms
Tebuconazole
Transformation pathways
Transformation products
Soils
1 (4 chlorophenyl) 4 methyl 3 (1,2,4 triazol 1 ylmethyl)pentan 3 ol
1 (4 chlorophenyl) 4,4 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentan 3 ol
1 (4 chlorophenyl) ethanone
1 (4 clorophenyl) 3 (1,2,4 triazol 1 ylmethyl)pentan 3 ol
1h 1,2,4 triazole
2 (1,2,4 triazol 1 yl)acetic acid
2 (1,2,4 triazol 1 yl)ethane 1,1 diol
2 hydroxy 3,3 dimethyl 2 (1,2,4 triazol 1 ylmethyl)butanoic acid
2,2 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentan 3 ol
3 hydroxy 4,4 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentanoic acid
3,3 dimethyl 1 (1,2,4 triazol 1 yl)butan 2 one
4 hydroxy 5,5 dimethyl 4 (1,2,4 triazol 1 ylmethyl)hexanoic acid
4 [3 hydroxy 4,4 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentyl]benzene 1,2 diol
4 [3 hydroxy 4,4 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentyl]phenol
5 (4 chlorophenyl) 2,2 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentane 1,3 diol
5 (4 chlorophenyl) 3 hydroxy 2 methyl 3 (1,2,4 triazol 1 ylmethyl)pentanoic acid
5 (4 chlorophenyl) 3 hydroxy 2,2 dimethyl 3 (1,2,4 triazol 1 ylmethyl)pentanoic acid
5 (4 chlorophenyl) 3 hydroxy 3 (1,2,4 triazol 1 ylmethyl)pentanoic acid
5 hydroxy 6,6 dimethyl 5 (1,2,4 triazol 1 ylmethyl)heptanoic acid
5 tert butyl 5 (1,2,4 triazol 1 ylmethyl) tetrahydrofuran 2 one
8 hydroxy 9,9 dimethyl 2 oxo 8 (1,2,4 triazol 1 ylmethyl)dec 4 enoic acid
benzene derivative
carbon
carbon 14
carbon dioxide
nitrogen
sulfur
tebuconazole
triazole derivative
unclassified drug
unindexed drug
fungicide
tebuconazole
triazole derivative
dissipation
ecotoxicology
laboratory method
mass spectrometry
polymerase chain reaction
relative abundance
soil biota
tebuconazole
transformation
winter
Article
bacterium
biogeochemical cycling
biotransformation
carbon cycling
chemical reaction kinetics
chemical structure
controlled study
ecotoxicity
incubation time
isotope labeling
laboratory
liquid chromatography-mass spectrometry
mass fragmentography
mass spectrometry
mineralization
nitrogen cycling
nonhuman
polymerase chain reaction
population abundance
priority journal
prokaryote
Proteobacteria
quantitative analysis
respirometry
simulation
soil and soil related phenomena
soil dissipation
soil microflora
sulfur cycling
time of flight mass spectrometry
winter
analysis
microbiology
season
soil
soil pollutant
toxicity
Alphaproteobacteria
Bacteria (microorganisms)
Bacteroidetes
Prokaryota
Proteobacteria
Fungicides, Industrial
Seasons
Soil
Soil Microbiology
Soil Pollutants
Triazoles
Elsevier B.V.
Metadata display
Abstract
Tebuconazole (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.
URI
http://hdl.handle.net/11615/71297
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19705]

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