Method for measuring virulence by feeding Bemisia tabaci Gennadius imago
A technology for bemisia tabaci and adults, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of mesophyll damage and withering, easy mold of agar, high probability of bemisia tabaci sticking to agar, etc., to achieve The effect of avoiding death, prolonging the fresh-keeping period, and avoiding non-toxic death
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Embodiment 1
[0019] Embodiment 1: (poinsettia raises whitefly adult and carries out the method for virulence determination)
[0020] (1) Preparation and sterilization of synthetic medium: Weigh 7g of agar, heat it, dissolve it in 500mL of distilled water with stirring, and prepare an agar solution; then add 25mL of NH 4 NO 3 20mg / L, KNO 3 3mg / L, MgSO 4 ·7H 2 O2mg / L, KH 2 PO 4 2mg / L, anhydrous CaCl 2 1 mg / L and make up to 1 liter of nutrient solution with water, and stir evenly to form a synthetic medium; after autoclaving the synthetic medium at 121°C for 15-20 minutes, pour it separately on the ultra-clean workbench Put it into a sterilized flat-bottom glass test tube with a length×diameter×thickness of 30mm×25mm×1.5mm, put the glass test tube into a sterilized and dried wide-mouth glass bottle after cooling, seal it with sterile plastic paper, and set aside ;
[0021] (2) Chemical treatment of leaves, petiole disinfection and insertion: cut the fresh and tender leaves of the test...
Embodiment 2
[0024] Embodiment 2: (the eggplant raises the whitefly adult and carries out the method for virulence determination)
[0025] In this example, the preparation of the synthetic medium in step (1) is as follows: weigh 7.5g of agar and dissolve it in 500mL of distilled water to prepare an agar solution; then add 27.5mL of NH 4 NO 3 22.5mg / L, KNO 3 2mg / L, MgSO 4 ·7H 2 O 1mg / L, KH 2 PO 4 3mg / L, anhydrous CaCl 22 mg / L and make up to 1 liter of nutrient solution with water, stir evenly to form a synthetic medium; step (2) chemical treatment of leaves, petiole disinfection and insertion: cut the test material eggplant leaves and use 10% imidacloprid WP 2000 After the 1-fold dilution is processed and dried in the shade, the petiole is soaked in 50% carbendazim wettable powder 800-fold dilution for 10-20 seconds for disinfection; the remaining steps and processes are the same as in Example 1.
Embodiment 3
[0026] Embodiment 3: (the method that cotton raises Bemisia tabaci adults and carries out virulence assay)
[0027] In this example, the preparation of the synthetic medium in step (1) is as follows: weigh 8 g of agar and dissolve it in 500 mL of distilled water to prepare an agar solution; then add 30 mL of NH 4 NO 3 25mg / L, KNO 3 1mg / L, MgSO 4 ·7H 2 O3mg / L, KH 2 PO 4 1mg / L, anhydrous CaCl 2 3 mg / L and make up to 1 liter of nutrient solution with water, stir evenly to form a synthetic medium; step (2) chemical treatment of leaves, petiole disinfection and insertion: cut test material cotton leaves and use 10% imidacloprid WP 3000 After the 1-fold dilution is processed and dried in the shade, the petiole is soaked in 1000-fold dilution of 50% carbendazim wettable powder for 10-20 seconds for disinfection; the remaining steps and processes are the same as in Example 1.
[0028] Table 1 Synthetic culture medium mildew and leaf preservation
[0029]
[0030] Annotate: ...
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