2016
DOI: 10.3389/fpls.2016.00393
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Changes in Aggressiveness of the Ascochyta lentis Population in Southern Australia

Abstract: Anecdotal evidence identified a change in the reaction of the resistant lentil cv Nipper to ascochyta blight in South Australia in 2010 and subsequent seasons, leading to infection. This study investigated field reactions of lentil cultivars against Ascochyta lentis and the pathogenic variability of the A. lentis population in southern Australia on commonly grown cultivars and on parental germplasm used in the Australian lentil breeding program. Disease data recorded in agronomic and plant breeder field trials… Show more

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Cited by 25 publications
(48 citation statements)
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“…Parents of the mapping populations exhibit different level of resistance to A. lentis isolates, hence isolates which could most effectively distinguish between the parents were selected for application on mapping populations. AB resistance-specific screening of the germplasm panel was conducted using FT12013, which has been isolated recently and is known to have overcome the resistance of at least one of the resistance (R) genes present in cultivars Northfield and Nipper (Davidson et al, 2016). A sub-set of germplasm panel lines were further evaluated using multiple pathogen isolates (Supplementary Table 2).…”
Section: Methodsmentioning
confidence: 99%
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“…Parents of the mapping populations exhibit different level of resistance to A. lentis isolates, hence isolates which could most effectively distinguish between the parents were selected for application on mapping populations. AB resistance-specific screening of the germplasm panel was conducted using FT12013, which has been isolated recently and is known to have overcome the resistance of at least one of the resistance (R) genes present in cultivars Northfield and Nipper (Davidson et al, 2016). A sub-set of germplasm panel lines were further evaluated using multiple pathogen isolates (Supplementary Table 2).…”
Section: Methodsmentioning
confidence: 99%
“…The two ultrasonic humidifiers within each tent were switched on immediately after inoculation for 1 h and every day thereafter for 1 h to promote lesion development which continued until disease assessment could be performed. Disease incidence was assessed for each seedling 14 days after inoculation as percentage area of plant diseased (% APD), incorporating leaf and stem lesions (Davidson et al, 2016). …”
Section: Methodsmentioning
confidence: 99%
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