2006
DOI: 10.1111/j.1439-0434.2006.01055.x
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Characterization and Pathogenicity of Rhizoctonia spp. from Onion in Amasya, Turkey

Abstract: Forty-two isolates of Rhizoctonia spp. were obtained from onion in Amasya, Turkey. Of these, 29% were Rhizoctonia solani (AG-4), 69% were Waitea circinata var. zeae (Rhizoctonia zeae) and 2% were binucleate Rhizoctonia (AG-B). Most of the isolates were recovered from rhizosphere soil. In pathogenicity tests on onion, R. solani AG-4 caused the greatest disease severity, those of W. circinata var. zeae were moderately virulent but binucleate Rhizoctonia isolates were of low virulence. This is the first report of… Show more

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Cited by 23 publications
(19 citation statements)
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“…Alike, the most common occurrence of R. solani AG-4 isolates on cucumber, pepper and snap bean plants has also been reported from other countries by several workers (MIRMAJLESSI et al, 2012;HARATIANA et al, 2013). Colony characteristics of isolates belonging to R. solani AG-4 were found to be similar to those of other studies (SNEH et al, 1991;ERPER et al, 2006). After 3 weeks of incubation, all colonies of R. solani AG-4 became brown colour, and their sclerotia were generally grey-brown coloured at first, then became dark brown with age.…”
Section: Discussionsupporting
confidence: 78%
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“…Alike, the most common occurrence of R. solani AG-4 isolates on cucumber, pepper and snap bean plants has also been reported from other countries by several workers (MIRMAJLESSI et al, 2012;HARATIANA et al, 2013). Colony characteristics of isolates belonging to R. solani AG-4 were found to be similar to those of other studies (SNEH et al, 1991;ERPER et al, 2006). After 3 weeks of incubation, all colonies of R. solani AG-4 became brown colour, and their sclerotia were generally grey-brown coloured at first, then became dark brown with age.…”
Section: Discussionsupporting
confidence: 78%
“…Five millimeter diameter agar discs of the isolates cut from the margins of the growing colonies were placed 1 cm apart on opposite sides of the coverslips on WA. After 24-48 h incubation at 25°C, hyphal anastomosis was determined by transferring the coverslip onto a microscope slide and staining with Safranin O and 3% KOH using the Olympus CX31 compound microscope at 400X magnification (ERPER et al, 2006). All tester isolates used in this study were provided by Dr. Erkol Demirci, Karadeniz Technical University.…”
Section: Hyphal Anastomosismentioning
confidence: 99%
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