Abstract

Scab is an important disease of apple and its control depends almost exclusively on frequent use of fungicides. Primary scab infection in the spring assumes several steps: ascospore maturation, liberation of ascospores that become airborne, deposition on susceptible tissues, and infection. However, the spatial heterogeneity of ascospores within the tree canopy is unknown. Aerial concentration of ascospore (ACA), ascospore concentration in rain water (ACR) and ascospore deposition (AD) were therefore measured at six heights (20–257 cm from the ground) with rotating-arm air samplers, funnels, and greased glass slides, respectively, during five rain events in 2001 and in 2002. In addition, ACR and AD were measured at eight locations within tree canopy at 196 cm height. Apple scab was assessed at the end of the primary infection period in each sampling location within the apple tree. A similar experimental design was used in 2003 to study the spatial heterogeneity of both AD and primary scab lesions. ACA and AD decreased with increasing height, while ACR increased with increasing height. Based on both variance to mean ratio and the power law relationship in both years, the ACR was heterogeneous, while AD was heterogeneous only during the peaks of ascospore release. The ACR was significantly higher at the centre of the trees and the AD was significantly higher at the centre and at the western edge of the trees. Only the cumulative AD was significantly correlated with apple scab lesions at the same location (r = 0.83). In 2003, a similar pattern of spatial heterogeneity within the tree canopy was observed for AD and primary scab lesion counts and there was a linear relationship (R2 = 0.84) between these two variables. It was concluded that ACR and AD within the tree canopy are not randomly distributed at least during peaks of ascospore release and that AD is a good estimate of primary scab lesion development. This spatial heterogeneity should be considered when estimating ascospore deposition using mathematical models or when quantifying ascosporic inoculum using spore samplers.

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