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CropMonitor > Winter Wheat > Encyclopaedia > Fusarium Head Blight > Effect of fungicides on FHB pathogens  


EFFECT OF FUNGICIDE ON FHB PATHOGENS
 
Currently, there is no one fungicide on the market capable of giving 100% control of FHB.

To date the best control achieved is between 60 and 70%. However to achieve this level of control the fungicide needs to be applied at the correct time.
  • Optimal fungicide timing = five days pre or post inoculum arriving on the ear

This can be difficult to achieve and as a result fungicides should be used only as part of an integrated management program.

As part of a three-year project funded by the HGCA (Project Report No. 297), several trials have been carried out at CSL to investigate the effectiveness of fungicides against FHB. Unless otherwise stated the results presented are from CSL trials.

The trials were carried out on plots artificially inoculated with a mixed conidial suspension containing F. culmorum, F. graminearum, F. avenaceum, F. poae and M. nivale vars nivale and majus. Plot humidity was maintained at a level greater than 70% for five days following inoculation.

Grain was analysed at the John Innes Centre for the presence of FHB pathogens using competitive PCR. Results from trials carried out between 1999 and 2001 are presented.


1999
The effect of a range of fungicides applied at full rate was investigated. All fungicides were applied two days post inoculation.

Fungicides applied were difenoconazole (as �Plover� at 0.3 l/ha), kresoxim-methyl + epoxiconazole (as �Landmark� at 1 l/ha), metconazole (as �Caramba� at 1.5 l/ha), carbendazim (as �Derosal WDG� at 400 g/ha), azoxystrobin (as �Amistar� at 1 l/ha), tebuconazole (as �Folicur� at 1 l/ha) and prochloraz (as �Sportak� at 0.9 l/ha).



  • M. nivale DNA was not found in any of the samples analysed by PCR.

  • Significant reductions in the levels of F. culmorum, F. graminearum and F. avenaceum DNA were seen following applications of tebuconazole, carbendazim, prochloraz or metconazole.

  • Azoxystrobin was ineffective against any of the true fusaria.

 
2000
The effects of fungicide rate and fungicide mixtures were investigated. All fungicides were applied two days post inoculation.

Fungicides applied were tebuconazole (as �Folicur� at 1 l/ha and 0.5 l/ha), metconazole (as �Caramba� at 1.5 l/ha and 0.75 l/ha), azoxystrobin (as �Amistar� at 1 l/ha and 0.5 l/ha), kresoxim-methyl + epoxiconazole (as �Landmark� at1 l/ha), epoxiconazole (as �Opus� at 1 l/ha and 0.5 l/ha), tebuconazole + azoxystrobin (as �Folicur� and �Amistar� both at 0.5 l/ha), metconazole + azoxystrobin (as �Caramba� and �Amistar� at 0.75 l/ha and 0.5 l/ha respectively), and epoxiconazole + azoxystrobin (as �Opus� and �Amistar� both at 0.5 l/ha).

CSL, York
graph

  • The predominant species detected by PCR was F. graminearum. High levels of F. culmorum and low levels of M. nivale DNA were also detected.

  • Full rate applications were more effective than reduced rate applications.

  • Application of a triazole fungicide significantly reduced the levels of F. culmorum and F. graminearum DNA.

  • Application of a triazole fungicide had no effect on the level of M. nivale DNA detected compared to the untreated control.

  • Application of azoxystrobin significantly reduced levels of M. nivale DNA.

  • Of the mixtures both tebuconazole and metconazole mixed with azoxystrobin significantly reduced the levels of F. culmorum, F. graminearum and M. nivale DNA detected.



Morley Research Centre, Wymondham, Norfolk
graph

  • The predominant pathogen DNA detected by PCR was M. nivale. Relatively low levels of F. culmorum and F. graminearum were also detected.

  • The application of a triazole reduced levels of F. culmorum and F. graminearum DNA detected. However no fungicide application gave a significant reduction.

  • Where azoxystrobin was applied, either as a straight formulation or as part of a mixture, levels of M. nivale DNA were significantly reduced.

 
2001
The effect of fungicide rate and application timing on FHB pathogens was investigated. Fungicides were applied to plots either 2 days pre-inoculation (S1) or 2 days post-inoculation (S2). Levels of inoculum used to artificially infect the plots were reduced compared to previous years in order to achieve disease levels comparable to a natural infection.

Fungicides applied were tebuconazole (as 'Folicur' at 0.5 l/ha and 0.25 l/ha), azoxystrobin (as 'Amistar' at 0.5 l/ha and 0.25 l/ha) and tebuconazole + azoxystrobin (as 'Folicur' and 'Amistar' both at 0.5 l/ha and 0.25 l/ha).

graph

  • F. culmorum was the predominant pathogen. No M. nivale DNA was found in any of the samples.

  • All fungicide treatments, with the exception of the post-inoculation azoxystrobin (0.25 l/ha) treatment, significantly reduced the level F. culmorum DNA compared to the control plots.

  • Fungicide treatment did not significantly affect any other Fusarium species.

  • Levels of FHB pathogen DNA were much lower than in previous years. Reducing the level of inoculum applied to the ear reduced the differences in fungicide efficacy seen in previous years.


 
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