2013
DOI: 10.1094/pdis-06-12-0606-re
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Characterization of the Bull's Eye Rot of Apple in Chile

Abstract: Soto-Alvear, S (Soto-Alvear, Sylvana)[ 1,2 ] ; Lolas, M (Lolas, Mauricio)[ 2 ] . Univ Talca, Fac Ciencias Agr, Talca, Chile.Soto-Alvear, S., Lolas, M., Rosales, I. M., Chavez, E. R., and Latorre, B. A. 2013. Characterization of the bull's eye rot of apple in Chile. Plant Dis. 97:485-490. Apple fruit in Chile are primarily produced for export to Asia, Europe, and the United States, which typically requires 15 to 40 days of maritime transportation. Therefore, Chilean apple production must fulfill the sanitizatio… Show more

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Cited by 40 publications
(52 citation statements)
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“…Because of the difficulty in obtaining conidia on culture media, apple fruits inoculated with P. vagabunda were used to induce conidial production with successful results in accordance with previous reports (Guthrie, ; Soto‐Alvear et al ., ; Hortova et al ., ). Moreover, the time needed to produce conidia in apple fruit (30 days) coincides with that observed by Guthrie ().…”
Section: Discussionmentioning
confidence: 96%
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“…Because of the difficulty in obtaining conidia on culture media, apple fruits inoculated with P. vagabunda were used to induce conidial production with successful results in accordance with previous reports (Guthrie, ; Soto‐Alvear et al ., ; Hortova et al ., ). Moreover, the time needed to produce conidia in apple fruit (30 days) coincides with that observed by Guthrie ().…”
Section: Discussionmentioning
confidence: 96%
“…() and Verkley (). However, slight differences in conidial size were observed in comparison with those obtained by several authors following the same protocol (Soto‐Alvear et al ., ; Chen et al ., ). In addition, the measurements obtained here were similar to those obtained by Rooney‐Latham et al .…”
Section: Discussionmentioning
confidence: 99%
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“…(), with the forward Neofab‐upTub‐100 primer corrected by Soto‐Alvear et al . (), was used for the amplification of DNA isolated from pure cultures of 19 isolates, previously identified on the basis of their β ‐tubulin sequences in this study. In PCR with the proposed primer set and an annealing temperature of 58°C, a product of the same size as that for N. alba was also observed for DNA of M. fructicola .…”
Section: Resultsmentioning
confidence: 99%
“…() for Neofabraea spp., with the corrected Neofab‐upTub‐100 primer at the 3′‐end, as suggested by Soto‐Alvear et al . (). The amplification conditions were as follows: an initial denaturation at 94°C for 3 min, followed by 35 cycles of denaturation at 94°C for 30 s, annealing at 58°C for 30 s, polymerization at 72°C for 45 s, and an extension step at 72°C for 5 min.…”
Section: Methodsmentioning
confidence: 97%