2015
DOI: 10.1007/s10658-015-0739-z
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An easy, rapid and accurate method to quantify plant disease severity: application to phoma stem canker leaf spots

Abstract: International audienceAssessing plant disease severity and pathogen population size is central to epidemiological studies that help to devise disease control practices for crop protection. Among current methods, there is a trade-off between accuracy, defined as the closeness of the estimated value to the true value, and cost, defined as the consumption of resources that have to be spent in order to achieve the appropriate measurement. On the one hand, accurate methods based on counting lesion numbers per plant… Show more

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Cited by 9 publications
(8 citation statements)
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“…Estimates of disease severity at the leaf spot stage (start of the epidemic) were obtained from counts of blackleg leaf spots on canola plants in 1 min from one square metre (lesions counted m −2  min −1 ; Bousset et al., 2016) on 15 July. For each field plot, three observers counted leaf spots on green leaves while moving at constant speed (2 m per min) sideways along the length of a delimited 0.5 × 2 m area.…”
Section: Methodsmentioning
confidence: 99%
“…Estimates of disease severity at the leaf spot stage (start of the epidemic) were obtained from counts of blackleg leaf spots on canola plants in 1 min from one square metre (lesions counted m −2  min −1 ; Bousset et al., 2016) on 15 July. For each field plot, three observers counted leaf spots on green leaves while moving at constant speed (2 m per min) sideways along the length of a delimited 0.5 × 2 m area.…”
Section: Methodsmentioning
confidence: 99%
“…That is, the objective of the studies is to collect reliable data for testing purposes (so the need is to consider reliability and cost—selecting the number of specimens and replicate (or sub-samples) estimates per sample to ensure sufficient reliability or agreement, while minimizing cost). Bousset et al ( 2016 ) also pointed out that, with given limited resources, cost is an important consideration in plant pathological studies. Chiang et al ( 2016b ) presented the concepts applied in medical research (Giraudeau and Mary 2001 ; Shoukri et al 2003 ; Shoukri 2004 ) and concluded that developing an optimal experimental design in which the number of specimens (individual units sampled) and the number of replicates (sub-sample) estimates per specimen for a fixed total number of observations (total sample size for the treatments being compared) are chosen to maximize statistical power and efficiency.…”
Section: Applications and Effects Of Quantitative Ordinal Scalesmentioning
confidence: 99%
“…In that context, the necessary epidemic data are generally difficult, costly and time-consuming to acquire (Bousset et al, 2015(Bousset et al, , 2016. Furthermore, as the direct quantification of the pathogen (or inoculum) and the infectiousness status of hosts plants (Susceptible, Latent, Infectious, Removed) are still challenging for plant diseases, they are indirectly inferred from pathology status data (Leclerc et al, 2014), often insufficient for testing mechanistic models without resorting to timeconsuming Bayesian methods (Bousset et al, 2015).…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, as the direct quantification of the pathogen (or inoculum) and the infectiousness status of hosts plants (Susceptible, Latent, Infectious, Removed) are still challenging for plant diseases, they are indirectly inferred from pathology status data (Leclerc et al, 2014), often insufficient for testing mechanistic models without resorting to timeconsuming Bayesian methods (Bousset et al, 2015). In this context, developing high-throughput and high-precision phenotyping methods appears as a main challenge for plant disease pathology and epidemiology (Bousset et al, 2016;Simko et al, 2016). For instance, as already shown by several authors, image-based phenotyping can be useful for detecting and quantifying disease symptoms (Camargo and Smith, 2009;Mahlein, 2016) and automated image processing enables one to expand substantially the throughput of disease data (Karisto et al, 2018;Stewart et al, 2016) which may feed modelling approaches and support empirical studies.…”
Section: Introductionmentioning
confidence: 99%