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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Journal of the Scien...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Journal of the Science of Food and Agriculture
Article . 2020 . Peer-reviewed
License: Wiley Online Library User Agreement
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Dissipation and residue determination of fluopyram and its metabolites in greenhouse crops

Authors: Marta Vargas‐Pérez; Francisco Javier Egea González; Antonia Garrido Frenich;

Dissipation and residue determination of fluopyram and its metabolites in greenhouse crops

Abstract

AbstractBACKGROUNDFluopyram is a pesticide widely used in tomato and cucumber crops cultivation to control fungal diseases that develop especially in environments with moderate temperatures and high humidity, such as in a greenhouse. The pathway of fluopyram dissipation has been monitored in cucumber and cherry tomato under greenhouse conditions.RESULTSIn the greenhouse trials, cherry tomato and cucumber were treated by irrigation water with the commercial product at the manufacturer’s recommended dose and double dose. High‐resolution mass spectrometry (HRMS) coupled to ultra‐high‐performance liquid chromatography (UHPLC) has been selected as the technique to obtain the identification of fluopyram and metabolites. The fate of fluopyram in greenhouse tomato and cucumber was investigated over 44 days. The metabolic pathway of fluopyram was: in a first step there was a primary transformation to fluopyram‐7‐hydroxy and fluopyram‐8‐hydroxy, isomeric compounds, and in a second phase to fluopyram‐benzamide and fluopyram‐pyridyl‐carboxylic acid. The behavior of fluopyram does not fit any type of kinetic classical model of degradation.CONCLUSIONSGreenhouse trials revealed that the fluopyram is a very persistent compound, and their terminal residues do not exceed maximum residue level (MRL) at the end of the study. © 2020 Society of Chemical Industry

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Keywords

Crops, Agricultural, Molecular Structure, Pyridines, Pesticide Residues, Fungicides, Industrial, Kinetics, Solanum lycopersicum, Tandem Mass Spectrometry, Fruit, Benzamides, Cucumis sativus, Chromatography, High Pressure Liquid

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Powered by OpenAIRE graph
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
25
Top 10%
Top 10%
Top 10%
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