2022
DOI: 10.3390/agronomy12020258
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Impact of Diversified Chemical and Biostimulator Protection on Yield, Health Status, Mycotoxin Level, and Economic Profitability in Spring Wheat (Triticum aestivum L.) Cultivation

Abstract: Biostimulators with chemical protection are a challenge in sustainable agriculture to obtain high yield, healthy, and pesticide-free wheat. The aim of this four-year spring wheat field experiment was to assess the effectivity of using herbicide, mixed fungicides protection, and a humic biostimulator. The following treatments were tested: biostimulator (S), sulfosulfuron (H), H + S, H + propiconazole + cyproconazole/spiroxamin + tebuconazole + triadimenol (H + F1 + F2), and H + F1 + F2 + S. Evaluations of wheat… Show more

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Cited by 23 publications
(25 citation statements)
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“…Looking at the work of other authors, mainly UHPLC, but also HPLC analytical columns with variations of C18 packing materials were used for chromatographic separation of analytes, maintained at 25–40 °C, with a mobile phase flow of 0.3–1.0 mL/min, mostly consisting of H 2 O and MeOH with the addition of modifiers (AFNH 4 , AA, FA, HAc, etc.) [ 8 , 16 , 25 , 28 , 29 , 30 , 31 , 32 , 33 ], confirming MeOH as more suitable for mycotoxin chromatographic separation. In addition, a relatively high percentage (≥75%) of the aqueous mobile phase in the initial conditions was generally maintained, and the injection volume was kept at no more than 20 µL, depending on the column type.…”
Section: Resultsmentioning
confidence: 88%
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“…Looking at the work of other authors, mainly UHPLC, but also HPLC analytical columns with variations of C18 packing materials were used for chromatographic separation of analytes, maintained at 25–40 °C, with a mobile phase flow of 0.3–1.0 mL/min, mostly consisting of H 2 O and MeOH with the addition of modifiers (AFNH 4 , AA, FA, HAc, etc.) [ 8 , 16 , 25 , 28 , 29 , 30 , 31 , 32 , 33 ], confirming MeOH as more suitable for mycotoxin chromatographic separation. In addition, a relatively high percentage (≥75%) of the aqueous mobile phase in the initial conditions was generally maintained, and the injection volume was kept at no more than 20 µL, depending on the column type.…”
Section: Resultsmentioning
confidence: 88%
“…The dilute-and-shoot principle of sample preparation in mycotoxin determination has also been applied by other authors [ 8 , 16 , 25 , 30 , 31 ], performed using solvent mixtures consisted of H 2 0, ACN and/or MeOH, and FA or HAc, but often in combination with sample extract evaporation and reconstitution. The Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) approach was also frequently employed [ 28 , 32 , 33 ]), consisting of acidic acetonitrile extraction/salt mixture partitioning and clean-up by dispersive solid phase extraction, and in certain cases followed by evaporation and reconstitution using a suitable solvent. Compared to the sample preparation methods developed by the aforementioned authors for the analysis of a similar scope of analytes and matrices [ 28 , 29 , 30 , 33 ], the method developed in this work has the same or shorter extraction time for the same analytes, a cheaper preparation procedure and shorter overall sample preparation time, since it does not involve evaporation or reconstitution steps.…”
Section: Resultsmentioning
confidence: 99%
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“…The Fusarium species spectra associated with FHB of barley appear be different than that affecting wheat. Fusarium graminearum is typically considered the most prevalent and aggressive FHB pathogen of wheat in the temperate and warmer regions of the United States and Canada [ 31 , 32 ], while in cooler regions of Europe F. graminearum , F. culmorum and F. avenaceum are predominant [ 33 ]. Therefore, research on Fusarium pathogens associated with FHB of barley in these regions has primarily focused on F. graminearum .…”
Section: Discussionmentioning
confidence: 99%
“…Besides the significant decrease in wheat yield, F. pseudograminearum produces a diverse array of toxic secondary metabolites including mycotoxins [ 10 , 11 ]. Cereals contaminated with mycotoxins are unsuitable for food or feed [ 12 , 13 ]. The mycotoxins produced by Fusarium include trichothecenes, fumonisins, etc.…”
Section: Introductionmentioning
confidence: 99%