Method for preventing and treating corn field armyworms
A technology for cornfield and armyworm, which is applied in the field of armyworm control and cornfield armyworm control, can solve the problems such as lagging research on armyworm insecticidal activity, achieve shortening the time required for prevention and control, good application prospects, and high activity Effect
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Embodiment 1
[0028] Pathogenicity of entomopathogenic nematode HB to armyworm
[0029]Add 30g of sterilized soil (humidity about 18%, pass through a 40 mesh sieve) into a 9.5cm glass culture dish, put 20 healthy, uniform 3rd instar armyworm larvae, and put in an appropriate amount of fresh corn leaves as feed; Dilute the HB nematode infection stage larvae with sterile water into six concentration gradients of 20IJs / mL, 30IJs / mL, 50IJs / mL, 75IJs / mL, 100IJs / mL, and 125IJs / mL; take 1mL nematode suspension for each concentration Evenly drop into the Petri dish. Three replicates were set up for each concentration, and sterile water was used as a control. Each treatment was placed in an incubator with a constant temperature of 25°C and a relative humidity of 80%. Add corn leaves in time as needed, observe and record the death of armyworm every 24h, and count after the 6th day of nematode infection, the results are obtained by figure 1 Shown: The death rate of armyworm increases with the incre...
Embodiment 2
[0031] Determination of Toxicity of Bt Strain HD1 to Armyworm
[0032] Dilute the quantified Bt strain HD1 with sterile water to 1.5×10 11 CFU / mL, 3×10 11 CFU / mL, 1.5×10 12 CFU / mL, 3×10 12 CFU / mL, 1.5×10 13 CFU / mL, 3×10 13 CFU / mL six concentration gradients. Add about 30g of sterilized soil (humidity about 18%, pass through a 40-mesh sieve) into a glass petri dish with a diameter of 9.5cm, soak the fresh corn leaves in the bacterial suspension of each concentration for about 1min, dry naturally, and take an appropriate amount Put them into petri dishes, and insert 20 healthy, uniform 3rd instar armyworm larvae into each dish. Each treatment was repeated 3 times while soaking in sterile water as a control. Each treatment was placed in an incubator with a constant temperature of 25°C and a relative humidity of 80%. Add in time the maize leaf after soaking bacteria solution and dry as required, and observe and record the death situation of armyworm every 24h. The results...
Embodiment 3
[0034] Toxicity determination of Bt strain G03 to armyworm
[0035] Assay method is the same as in Example 2, and the Bt bacterial strain G03 quantified is diluted to 0.5 × 10 with sterile water. 11 CFU / mL, 1×10 11 CFU / mL, 5×10 11 CFU / mL, 1×10 12 CFU / mL, 5×10 12 CFU / mL, 1×10 13 CFU / mL six concentration gradients, the indoor toxicity test results of Bt strain G03 to armyworm are as follows Figure 4 Shown: With the increase of Bt concentration, the death rate of armyworm gradually increased, 5.0×10 12 The CFU / mL concentration of Bt showed a slow increase in the death rate of armyworm after 3 days of treatment (P>0.05), and the death rate of armyworm reached 96.67%, 1.0×10 13 Under the high concentration of CFU / mL, the death rate of armyworm reached 100%; 5.0×10 11 CFU / mL, 1.0×10 12 The CFU / mL concentration of Bt showed a slow increase in armyworm mortality after 4 days of treatment (P>0.05), and the armyworm mortality rate reached 80%; 0.5×10 11 After 4 days of treatm...
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