2015
DOI: 10.1094/pdis-05-14-0490-re
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Relationship of Airborne Botrytis cinerea Conidium Concentration to Tomato Flower and Stem Infections: A Threshold for De-leafing Operations

Abstract: Carisse, O., and Van der Heyden, H. 2015. Relationship of airborne Botrytis cinerea conidium concentration to tomato flower and stem infections: A threshold for de-leafing operations. Plant Dis. 99:137-142.Gray mold, caused by Botrytis cinerea, is an important threat for toma to greenhouse producers. The influence of airborne conidia concentra tion (ACC) on both flower and stem-wound infections was studied in a greenhouse maintained at a temperature of 15, 20, or 25°C using dis eased tomato leaves as the uniqu… Show more

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Cited by 22 publications
(19 citation statements)
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“…Fr., is known to be the most important postharvest pathogen causing gray mold of table grapes [5,6]. Infection caused by this fungus remains inactive in the field unless it gets favorable environmental conditions, i.e., fruit injuries that assist pathogen development [7,8]. Even a small infection on a single berry can damage the whole lot of grapes, and if it is not noticed at pre-harvest stage, during packaging, or during shipment, it may progress and spread the infection in postharvest or during the cold storage period of table grapes, even at low temperatures [9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…Fr., is known to be the most important postharvest pathogen causing gray mold of table grapes [5,6]. Infection caused by this fungus remains inactive in the field unless it gets favorable environmental conditions, i.e., fruit injuries that assist pathogen development [7,8]. Even a small infection on a single berry can damage the whole lot of grapes, and if it is not noticed at pre-harvest stage, during packaging, or during shipment, it may progress and spread the infection in postharvest or during the cold storage period of table grapes, even at low temperatures [9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…The pieces were dried between sterile filter paper, inoculated on PDA plates and incubated at 28 ± 2 °C for 3–7 days. Subsequently, single hyphal tips were repeatedly transferred to fresh PDA plates and incubated at 28 ± 2 °C for 5 days under a 16‐h photoperiod to obtain pure cultures . The purified strains were maintained in a refrigerator (4 °C) until further use.…”
Section: Methodsmentioning
confidence: 99%
“…The pieces were dried between sterile Whatman No.1 filter paper and cultured on water agar plates and incubated at 28±2°C for 24 h. Single hyphal tips were transferred to Petri dishes containing V8 medium and incubated at 28±2°C for 5 days under a 12 h photoperiod (Carisse and Van Der Heyden, 2015). Purified cultures were visually identified utilizing laboratory manuals (Dugan, 2006).…”
Section: Isolation and Identification Of Pathogensmentioning
confidence: 99%