1. Introduction
Fusarium head blight (FHB) is one of the most important wheat diseases, as it causes the contamination of grain with mycotoxins. This reduces the yield and diminishes the quality of grain [
1,
2]. The spray deposition of a fungicide on wheat heads is an important factor of FHB suppression. Wheat heads are difficult to spray with a fungicide in a way to achieve its even coverage. Different studies show that uneven spray deposition occurs at the front and the rear sides of wheat heads [
3]. At the front side of heads, the achieved coverage is 20%, while at the rear side of heads, it is approximately 10% [
4]. The new spraying technologies rarely achieve more than 10% head fungicide coverage, while spraying with an airplane achieves only from 1 to 3% [
5]. Turbo FloodJet nozzles, which turn alternatively forward and back on the spray boom, can achieve 30% coverage, both at the front and the rear of wheat heads. In a three-year study, this nozzle achieved higher efficiency against FHB than the standard nozzles with a vertical jet [
6,
7]. The authors in [
2] established a 1.30–1.43-fold higher content of the active ingredient in heads after spraying with double nozzles, and a 1.08–1.34-fold higher content of the active ingredient in heads after spraying with the Turbo FloodJet nozzles, in comparison with the standard nozzles with a vertical jet. The application of nozzles with a backward spray jet and symmetric and asymmetric double flat fan nozzles achieved better coverage on the front and the rear side of wheat heads [
8,
9,
10,
11].
FHB can reduce yield by up to 30%, while the grain becomes infected with mycotoxins, particularly with deoxynivalenol (DON) [
12]. Conditions favourable to FHB can diminish the quality of grain, lower the absolute thousand grain weight, and bring about a higher percentage of tiny, scabby, and colored grain. The application of a fungicide with the active ingredients prothioconazole and tebuconazole can lower the DON value in the grain by 22–72% [
13,
14,
15]. The timely application of azole fungicides, which contain the active ingredients tebuconazole, metconazole, and prothioconazole, can reduce infections by 50–70% and mycotoxin content by 50–80%. In the experiment [
16], azole fungicide was used to lower the DON value in the grain of both common and durum wheat, the latter being more susceptible to FHB [
12]. It is reasonable to spray plants with fungicides up to 11 days after flowering if the inoculum is present at the time of spraying [
17].
The aim of this trial was to establish the effects of a low-volume application rate on the head fungicide coverage, the DON content in wheat grain, and yield. In the trial, an artificial inoculum was made with F. graminearum. The hypothesis was posed that a lower spraying pressure (2 bar), and consequently a lower volume application rate (117 L/ha), will produce a lower fungicide coverage of heads and leaves when spraying with a special TD VR nozzle with a bypass valve. This will result in lower yield, poorer grain quality, and higher mycotoxin DON content in the grain. We were interested in how insufficient head fungicide coverage influenced the DON value in the grain, and what the lower limit of volume application rate was when spraying wheat heads.
4. Conclusions
The experiment confirmed the hypothesis that head fungicide coverage increases at higher pressures. This holds true both in regard to the quality of spray deposition and the quantity of spray deposition on heads. At the pressure of 2 bar, in particular, a very low head fungicide coverage was achieved, both at the front and rear sides. Despite the poorer spray deposition on heads at the pressure of 2 bar, there were no significant differences in grain yield with the remaining spraying pressures, which is not in accordance with our hypothesis. Similarly, in the year 2019, with a more intense infection with FHB, at a poorer head fungicide coverage, and at a lower spraying pressure of 2 bar, no significant differences appeared in the DON value at the remaining spraying pressures. At the pressure of 2 bar, the DON value approached a maximum level, 1250 µg/kg, in 2019. Despite this, the DON value in the grain tended to decrease at an increased spraying pressure with an exponent function in 2019. In the grain quality parameters, the spraying pressure had no significant influence, so our hypothesis was not confirmed. However, a poorer spray deposition on heads lowered the thousand grain weight. This is manifested particularly in years with more intense infection. On the basis of the study, it is concluded that the choice of spraying pressures with a special double nozzle with a variable injector should be made according to climatic conditions during sensitive wheat growing stages (heading and flowering). Low spraying pressures and water volumes should be used when weather conditions are not favourable to FHB spreading. When weather conditions are suitable for FHB infection higher spraying pressures and water volumes should be applied. In order to confirm our results, future experiments should continue with a volume application rate even lower than 100 L/ha and with the application of a symmetric double flat fan nozzle.
5. Materials and Methods
5.1. Field Trial
In 2019 and 2020, a field trial was carried out at the laboratory field of the Biotechnical Faculty in Ljubljana, Slovenia. The experimental spraying against FHB involved variable injector nozzles with the double asymmetrical jet TurboDrop VR 1.5 produced by Agrotop. This nozzle has a special bypass valve, which constantly changes the intersection of outlet and thus the volume flow rate at the ratio 1:3 at the pressures from 2 to 8 bar, and at the ratio 1:6 at the pressures from 1 to 6 bar. The standard nozzles have a ratio of volume flow rate of 1:2 at pressures from 2 to 8 bar. The angle of the spraying jet is 120°. The front jet is directed forward in the direction of driving at an angle of 10° in relation to the vertical, while the back is directed backward at an angle of 50° in relation to the vertical [
36].
With these nozzles, three spraying pressures were applied, namely 2 bar, 4 bar, and 6 bar. At the spraying speed of 7 km/h and at the pressure of 2 bar, the volume application rate was 117 L/ha; it was 207 L/ha at the pressures of 4 bar, and it was 271 L/ha at the pressure of 6 bar. At the pressure of 2 bar, the volume median diameter (VMD) exceeded 550 µm, it ranged from 400 to 550 µm at the pressure of 4 bar, and it ranged from 350 to 400 µm (ASAE and BCPC) at the pressure of 6 bar.
The experimental design comprised random blocks with four repetitions. The trial involved three spraying pressures (2, 4, and 6 bar) and a control (untreated plants). The length of individual experimental unit was 19 m, and the width was 2.5 m. The spraying of wheat heads was carried out at the beginning of flowering (BBCH 61–63). In 2019, the spraying of heads was carried out on the 25th of May, and it was carried out on the 21st of May in the following year. During the spraying of heads in 2019, the precipitation was almost four times higher than in 2020, which meant significantly better conditions for the infection of heads with FHB (
Table 10). Otherwise, the entire amount of precipitation in the period October–July was similar, around 1000 mm in both years of the trial (
Table 11). The tractor sprayer Agromehanika AGS 600 EN was used, which was fitted with hydraulic spray booms. The driving speed during the spraying was 7 km/h. The spraying of heads involved the fungicide Prosaro with the active ingredients prothioconazole (125 g/L) and metconazole (125 g/L) at a dosage of 1 L/ha (Bayer AG, Germany). The wheat cultivar was Bastide, which is an awn wheat that is moderately susceptible to FHB. The precrop was winter wheat. In autumn, the plot was ploughed with a reversible plough.
Immediately before spraying, the water-sensitive papers (WSPs) were fixed to the front and the rear side of heads, on the flag leaf (Leaf 1), and on the two lower leaves (Leaves 2 and 3). Nine wheat heads, 9 flag leaves, 9 s leaves, and 9 third leaves were randomly chosen per plot. The spraying of heads was then carried out with the fungicide. With WSP, the quality of spray deposition on heads and on the first three leaves below the head was established.
Filter paper was placed on the front and the rear side of heads. The experimental plot was then sprayed with a colorant, a water solution of the colour Helios SC 500. First, the colour was dissolved in water in the sprayer’s tank via hydraulic mixing. The experimental plot was then sprayed as planned for the treatments. The procedure was repeated three times at each experimental unit. Thus, the amount of tracer deposit on the heads and the leaves of wheat was evaluated. The analysis of the deposit was performed at the Slovenian Institute of Hop Research and Brewing in Žalec.
All agrotechnical tasks in the trial were performed in line with good agricultural practice. They included soil cultivation, sowing, fertilizing, and chemical plant protection.
5.2. Artificial Inoculation and Inoculum Production
Two hours after spraying the heads with the fungicide, the artificial infection with Fusarium graminearum was performed. The seeds infected with the said fungus were soaked in water and then sprayed with the battery sprayer Solo 416 Li on the experimental plots. The entire area was watered with artificial rain so as to increase the possibility of infection.
The F. graminearum isolate originated from the infected wheat seeds harvested in Slovenia in 2018. The pure fungal cultures were grown in petri dishes on one-third potato dextrose agar (PDA) with the pieces of filter paper placed at the surface of the medium to stimulate conidial production. Conidia were splashed from 14-day-old cultures with sterile tap water. The suspension was used to inoculate the sterilized wheat grains in glass containers. The inoculum was also transferred to petri dishes with the medium prepared as described above. After 16 days of incubation at 20–22 °C, exposed to natural light at the laboratory bench, sufficient sporulation was achieved. The grains and sporulating cultures were rinsed with sterile tap water, and the obtained conidial suspension was filtered through cheesecloth. The concentration of conidia was determined using a hemocytometer and adjusted to 2 × 105 conidia/mL.
5.3. WSP Analysis and Tracer Analysis
The analysis of WSPs was carried out with the Wise Node system, from the company Wise Technologies Ltd. Slovenia. The system consists of an industrial camera (Basler), which contains an accurate sensor (2 million pixels per picture; resolution: 1920 × 1080). The camera and the computer are connected via USB 3.0 cable. The camera is fixed on a mechanical structure. Three measurements were carried out on each measuring paper. On an individual measurement paper, the programme calculates the coverage value and the number of droplet impacts per 1 cm2. Thus, the quality of phytopharmaceutical product (PPP) deposition on the heads was established.
The method for measuring tracer deposit is based on determining the amount of the tracer Helios SC 500, which has fluorescent properties on collectors. An amount of 0.2 g of wheatears was cut by scissors cleaned with ethanol for each new individual sample in a beaker. Seven milliliters of solvent diethylene glycol monoethyl ether (Sigma-Aldrich, Germany) were added and extracted for 15 min in an ultrasonic bath (Bandelin Sonorex, Germany) at room temperature. Immediately after extraction, the liquid part was transferred into the vial and subjected to further analysis by HPLC.
Filter paper was cut by scissors cleaned with ethanol for each new individual sample in a beaker. Two milliliters of solvent 2-ethoxyethanol (Sigma-Aldrich Chemie GmbH, Munich, Germany) were added and extracted for 15 min in an ultrasonic bath (Bandelin electronic GmbH & Co. KG, Berlin, Germany) at room temperature. Immediately after extraction, the liquid part was transferred into the vial and subjected to further analysis by HPLC.
Approximately 0.2 g of wheat leaves were cut by scissors cleaned with ethanol for each new individual sample in a beaker. Two milliliters of solvent diethylene glycol monoethyl ether (Sigma-Aldrich Chemie GmbH, Munich, Germany) was added and extracted for 15 min in an ultrasonic bath (Bandelin electronic GmbH & Co. KG, Berlin, Germany) at room temperature. Immediately after extraction, the liquid part was transferred into the vial and subjected to further analysis by HPLC.
Ten microliters of the obtained extract was injected into the liquid chromatograph equipped with a fluorescence detector (Agilent Technologies, Inc. Headquarters, Santa Clara, CA, USA) and without any column. The isocratic mobile phase (2-ethoxyethanol for paper collectors and diethylene glycol monoethyl ether for plant tissues) with a flow of 0.7 mL/min was used. The excitation energy with a wavelength of 375 nm was used; emitted light was detected at a wavelength of 435 nm. The amount of tracer in the collector was calculated externally from the calibration curve prepared with standard solutions of tracer in solvents used for extraction.
5.4. Yield and Yield Parameters
The harvest was carried out with a Wintersteiger plot harvester with a working width of 1.5 m. The moisture of the grain was measured with the Pfeuffer HE 40 moisture meter. The yield was calculated at 14% moisture. On each experimental plot, 8 samples of 1000 kernels were weighted using the ABS-N Kern analytic scale with an accuracy of 0.1 mg to measure the thousand grain weight. In addition, 100 g of grain were poured through a sieve, and the percentages of grain sizes >4 mm, 3–4 mm, 2.5–3 mm, 2–2.5 mm, and <2 mm were calculated. The thousand grain weight and the percentages of grain sizes were established for each plot in eight repetitions. The parameters of grain quality, such as the hectoliter weight, the protein percentage, the falling number, and the sedimentation value, were established by the Institute Bureau Veritas, according to standards SIST ISO 1871, SIST ISO 7971-2, and SIST ISO 3093. One measurement per plot was done.
5.5. DON Analysis
The grain samples were collected manually from the heads before the harvest and flailed with a Wintersteiger thresher. The analysis of the DON was performed with the ROSA FAST5 DON Quantitative Test. A grain sample of 50 g is weighed, and 250 mL of deionized water is then added. The sample is then shaken for a maximum of 2 min and filtered through MN 615 filter paper. After that, a diluted extract is made of 100 µL of extract +1.0 mL of DONQ-FAST 5 dilution buffer. The test strips are placed in a ROSA incubator. The tape is peeled, and 300 µL of diluted extract is then pipetted into the sample compartment. The tape is resealed and incubated for 5 min. After that, the test strip is inserted into a ROSA-M Reader for measuring DON content. The test strip should be measured within 1 min after incubation. The measuring range is between 0 and 1.5 ppm. If the measured value is higher, another diluted extract is prepared from 300 µL of diluted extract + 1.0 mL of DONQ-FAST 5 dilution buffer. The subsequent procedure is the same and the measuring range is between 0 and 6 ppm (Charm Sciences, Inc. Headquarters, Lawrence, USA).
5.6. Data Analysis
The statistical analysis was carried out with the programme Statgraph 4.0. The analysis of variance for random blocks was carried out. Duncan’s multiple comparison test was used for establishing the differences between means. The degree of risk was 0.05. The statistical differences between the treatments were presented with different letters. The relationship between the DON content in the grain and the spraying pressure was presented with a regression model. First, the most suitable model was determined. The individual parameters of the model were then calculated, and the analysis of variance was then applied. The F-test, the coefficient of determination, and the coefficient of correlation were calculated. The Pearson correlation coefficients were also calculated for different variables.