1974
DOI: 10.1080/03015521.1974.10425758
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Laboratory evaluation of fungicides against fungi causing flower blight of chrysanthemums

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Cited by 8 publications
(5 citation statements)
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“…Using a poisoned food technique [ 26 ], different fungicides were tested for their ability to prevent the growth of the R. solani isolate. Three fungicides were used: Uniform ® (active ingredient: Azoxystrobin 28.2% ( w / w ) and Mefenoxam 10.8% ( w / w ), Syngenta, Wilmington, Delaware, USA), Rizolex ® (active ingredient: Tolclofos-methyl 50 % ( w / w ) WP, Sumitomo Chemical Corp., Nihonbashi, Chuo-ku, Tokyo, Japan), and Hattrick ® (active ingredient: Tebuconazole 6% FS, Shoura chemicals, Egypt).…”
Section: Methodsmentioning
confidence: 99%
“…Using a poisoned food technique [ 26 ], different fungicides were tested for their ability to prevent the growth of the R. solani isolate. Three fungicides were used: Uniform ® (active ingredient: Azoxystrobin 28.2% ( w / w ) and Mefenoxam 10.8% ( w / w ), Syngenta, Wilmington, Delaware, USA), Rizolex ® (active ingredient: Tolclofos-methyl 50 % ( w / w ) WP, Sumitomo Chemical Corp., Nihonbashi, Chuo-ku, Tokyo, Japan), and Hattrick ® (active ingredient: Tebuconazole 6% FS, Shoura chemicals, Egypt).…”
Section: Methodsmentioning
confidence: 99%
“…At 1000 µg/ml, mancozeb recorded only 74.44 per cent colony growth inhibition and thus was found less effective when compared to systemic triazole and strobilurin fungicides, as it did not record complete colony growth inhibition at such a higher concentration. Singh and Milne (1974) reported that mancozeb exhibited high fungicidal activity at or below 100 µg/ml a.i. against A. alternata and S. vesicarium, while all the other fungicides viz., bavistin, benomyl, captafol, captan, carboxin, chloroneb, chlorothalonil, dicloran, fuberidazole, oxycarboxin, thiabendazole, thiophanate methyl, thiram and zineb were not effective.…”
Section: In Vitro Evaluation Of Different Fungicides Against Alternarmentioning
confidence: 99%
“…To perform the assay, agar plates containing desired amounts of the antimicrobial compound of interest and control plates devoid of the test compound are prepared [ 44 ]. Agar discs (3–6 mm) containing the test fungus are cut from the periphery of actively growing colonies and carefully placed at the center of the petri plates.…”
Section: Methods To Evaluate Antimicrobial Activitymentioning
confidence: 99%