2022
DOI: 10.1007/s10493-022-00719-6
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Evaluation of the entomopathogenic fungus Metarhizium brunneum and the predatory mite Stratiolaelaps scimitus against Rhizoglyphus robini under laboratory conditions

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Cited by 3 publications
(2 citation statements)
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“…Muscardine cadaver larvae of S. litura were disinfected with 75% (v/v) anhydrous ethanol for 30 s and with 1% (v/v) sodium hypochlorite for 2 min; rinsed with sterile water three times; the surface water was absorbed with a sterile filter paper; cut into five sections using a sterile scalpel; placed on Potato Dextrose Agar (PDA) medium (Sangon Biotech, Shanghai, China), which contained 1 mL ampicillin per liter at a concentration of 100 μg/mL; and incubated in a constant temperature incubator at 26°C for 5–7 days until mycelium grew. The strain was purified by the single-spore isolation method as described previously ( Ghalehgolabbehbahani et al, 2022 ), and the purified strain was designated AnS1Gz1-1.…”
Section: Methodsmentioning
confidence: 99%
“…Muscardine cadaver larvae of S. litura were disinfected with 75% (v/v) anhydrous ethanol for 30 s and with 1% (v/v) sodium hypochlorite for 2 min; rinsed with sterile water three times; the surface water was absorbed with a sterile filter paper; cut into five sections using a sterile scalpel; placed on Potato Dextrose Agar (PDA) medium (Sangon Biotech, Shanghai, China), which contained 1 mL ampicillin per liter at a concentration of 100 μg/mL; and incubated in a constant temperature incubator at 26°C for 5–7 days until mycelium grew. The strain was purified by the single-spore isolation method as described previously ( Ghalehgolabbehbahani et al, 2022 ), and the purified strain was designated AnS1Gz1-1.…”
Section: Methodsmentioning
confidence: 99%
“…Isolation and culture of the EPF strain M. rileyi-killed larvae of S. litura were disinfected with 75% (v/v) anhydrous ethanol for 30 s, 1% sodium hypochlorite for 2 min, rinsed with sterile water three times, surface water was absorbed with sterile filter paper, cut into five sections used a sterile scalpel, placed on potato dextrose agar (PDA) medium (Sangon Biotech, Shanghai, China) containing 1 mL of ampicillin per liter at a concentration of 100 μg mL −1 , and incubated in a constant temperature incubator at 26 °C for 5-7 days until mycelium grew. 27 The strain was purified by the single-spore isolation method as described previously, 29 and the purified strain was designated MrS1Gz1-1.…”
Section: 21mentioning
confidence: 99%