@misc{marin_romero_guzman_sutton_2003, title={Black sigatoka: An increasing threat to banana cultivation}, volume={87}, ISSN={["1943-7692"]}, DOI={10.1094/PDIS.2003.87.3.208}, abstractNote={HomePlant DiseaseVol. 87, No. 3Black Sigatoka: An Increasing Threat to Banana Cultivation PreviousNext OPENOpen Access licenseBlack Sigatoka: An Increasing Threat to Banana CultivationDouglas H. Marín, Ronald A. Romero, Mauricio Guzmán, and Turner B. SuttonDouglas H. MarínSearch for more papers by this author, Ronald A. RomeroSearch for more papers by this author, Mauricio GuzmánSearch for more papers by this author, and Turner B. SuttonCorresponding author: Turner B. Sutton, North Carolina State University, Raleigh; E-mail: E-mail Address: [email protected]Search for more papers by this authorAffiliationsAuthors and Affiliations Douglas H. Marín , Del Monte Fresh Produce Ronald A. Romero , Chiquita Brands Mauricio Guzmán , National Banana Corporation of Costa Rica Turner B. Sutton , North Carolina State University, Raleigh Published Online:23 Feb 2007https://doi.org/10.1094/PDIS.2003.87.3.208AboutSectionsPDF ToolsAdd to favoritesDownload CitationsTrack Citations ShareShare onFacebookTwitterLinked InRedditEmailWechat DetailsFiguresLiterature CitedRelated Vol. 87, No. 3 March 2003SubscribeISSN:0191-2917e-ISSN:1943-7692 Metrics Article History Issue Date: 25 Jan 2008Published: 23 Feb 2007 Pages: 208-222 Information© 2003 The American Phytopathological SocietyPDF downloadCited byEffect of duration of mycelia fragmentation and concentration on virulence of Mycosphaerella fijiensis in banana16 June 2023 | Brazilian Journal of Science, Vol. 2, No. 11Leaf disease detection using machine learning and deep learning: Review and challengesApplied Soft Computing, Vol. 3Screening and Optimization of Fermentation Medium for Bacillus velezensis BP-1 and Its Biocontrol Effects against Peyronellaea arachidicola7 April 2023 | Applied Sciences, Vol. 13, No. 8High level of somatic mutations detected in a diploid banana wild relative Musa basjoo26 October 2022 | Molecular Genetics and Genomics, Vol. 298, No. 1Plant extracts as potential control agents of Black Sigatoka in banana7 September 2022 | Journal of Plant Pathology, Vol. 104, No. 4Prediction of Banana Production Using Epidemiological Parameters of Black Sigatoka: An Application with Random Forest29 October 2022 | Sustainability, Vol. 14, No. 21Plantain hybrids for the humid forest agroecology of Central Africa – diseases and pests load, fruit yield and farmers perception1 November 2022 | Plant Production Science, Vol. 25, No. 4The long road to a sustainable banana trade16 September 2022 | PLANTS, PEOPLE, PLANET, Vol. 18Regional disparities in impacts of climate extremes require targeted adaptation of Fairtrade supply chainsOne Earth, Vol. 5, No. 8Gene Expression, Histology and Histochemistry in the Interaction between Musa sp. and Pseudocercospora fijiensis27 July 2022 | Plants, Vol. 11, No. 15Novel mating-type-associated genes and gene fragments in the genomes of Mycosphaerellaceae and Teratosphaeriaceae fungiMolecular Phylogenetics and Evolution, Vol. 171Producing Crops without Mancozeb? 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Bandyopadhyay28 February 2007 | Plant Disease, Vol. 91, No. 3Evaluating the Performance of Chemical Control in the Presence of Resistant Pathogens18 July 2006 | Bulletin of Mathematical Biology, Vol. 69, No. 2Accumulation of Current-Use Pesticides in Neotropical Montane Forests10 January 2007 | Environmental Science & Technology, Vol. 41, No. 4Isolation and characterization of the mating type locus of Mycosphaerella fijiensis, the causal agent of black leaf streak disease of bananaMolecular Plant Pathology, Vol. 8, No. 1Distribuição e impacto da sigatoka-negra na bananicultura do estado do AcreFitopatologia Brasileira, Vol. 29, No. 5Mating and Pseudothecial Development in Mycosphaerella citri, the Cause of Citrus Greasy SpotS. N. Mondal, D. S. Howd, R. H. Brlansky, and L. W. Timmer5 February 2007 | Phytopathology®, Vol. 94, No. 9}, number={3}, journal={PLANT DISEASE}, author={Marin, DH and Romero, RA and Guzman, M and Sutton, TB}, year={2003}, month={Mar}, pages={208–222} }
 @article{romero_sutton_1998, title={Characterization of benomyl resistance in Mycosphaerella fijiensis, cause of black Sigatoka of banana, in Costa Rica}, volume={82}, DOI={10.1094/PDIS.1998.82.8.931}, abstractNote={Sixty-eight and eighty-six percent of monoascosporic isolates of Mycosphaerella fijiensis from two banana plantations in Costa Rica, in which benomyl was used for ≈10 years to control black Sigatoka, were resistant to benomyl in February and November 1994, respectively. No resistance to benomyl was detected in isolates collected during February 1994 from farms with no history of benomyl use that were located ≈50 km from the nearest banana plantations. Only 1% of isolates was resistant to benomyl in a sample taken during November 1994. In three additional banana farms where benomyl had not been used for 3 to 5 years before sampling, ben-omyl resistance persisted at a high frequency. Benomyl-resistant and -sensitive isolates were distributed equally throughout the range of isolate sensitivity to propiconazole, indicating no relationship between resistance to benomyl and lower sensitivity to propiconazole but double resistance to these two compounds. Five benomyl-resistant and five benomyl-sensitive isolates of M. fijiensis were inoculated to banana plants under greenhouse conditions. Benomyl-resistant isolates were more aggressive than benomyl-sensitive isolates, as determined by measures of disease severity, incubation time, and number of lesions at 40 days after inoculation.}, number={8}, journal={Plant Disease}, author={Romero, R. A. and Sutton, T. B.}, year={1998}, pages={931–934} }
 @article{romero_sutton_1997, title={Reaction of four Musa genotypes at three temperatures to isolates of Mycosphaerella fijiensis from different geographical regions}, volume={81}, ISSN={["1943-7692"]}, DOI={10.1094/PDIS.1997.81.10.1139}, abstractNote={Two tetraploid banana hybrids, FHIA1 and FHIA2, with resistance to black Sigatoka, and two highly susceptible, naturally occurring triploids, Grand Naine and False Horn, were evaluated at three temperatures for their resistance to isolates of Mycosphaerella fijiensis from five geographical regions. The youngest open leaf of young plants was inoculated, and plants were incubated at 22, 26, and 30°C in growth chambers. Duration of the incubation period and disease severity were used to evaluate the reactions of the genotypes. The incubation period was the shortest at 26°C. Disease severity was greatest at 26°C on Grand Naine and False Horn, but there was no clear temperature effect for the FHIA genotypes. The incubation period was longer on both FHIA genotypes than on Grand Naine and False Horn. With few exceptions, isolates with the shortest incubation periods caused greater disease severity than those with longer incubation periods. The level of resistance between the two FHIA genotypes was similar, and both expressed high resistance across temperatures and isolates of M. fijiensis, indicating that no physiological races of the pathogen were detected. There were differences in durations of the incubation periods and disease severities associated with the geographical origin of the isolates. Isolates that originated in Honduras, Colombia, and Costa Rica produced more disease on Grand Naine and False Horn than did isolates from Cameroon and Asia. However, no differences associated with the geographical origin of the isolates were observed for both FHIA genotypes. Also, there were no differences in disease severities within isolates that originated from Honduras, Colombia, and Costa Rica.}, number={10}, journal={PLANT DISEASE}, author={Romero, RA and Sutton, TB}, year={1997}, month={Oct}, pages={1139–1142} }
 @article{romero_sutton_1997, title={Sensitivity of Mycosphaerella fijiensis, causal agent of Black Sigatoka of Banana, to Propiconazole}, volume={87}, ISSN={["1943-7684"]}, DOI={10.1094/PHYTO.1997.87.1.96}, abstractNote={One hundred monoascosporic isolates of Mycosphaerella fijiensis were collected in February and November 1994 from each of two banana (Musa spp.) plantations in Costa Rica. Locations at San Pablo and Coopecariari had been sprayed with propiconazole for the past 7 years to control black Sigatoka. One hundred monoascosporic isolates from a third location, San Carlos, with no history of fungicide use, also were tested for sensitivity to propiconazole. Fifty percent effective concentration (EC 50 ) values were calculated for individual isolates by regressing the relative inhibition of colony growth against the natural logarithm of the fungicide concentration. In the February sample, the mean EC 50 values for San Pablo and Coopecariari populations were 0.06 and 0.05 μg a.i. ml -1 , respectively, which were not statistically different (P = 0.05). The mean EC 50 value of the population at San Carlos was 0.008 μg a.i. ml -1 , which was significantly lower (P = 0.001) than the mean EC 50 values obtained at San Pablo and Coopecariari. Frequency distributions of EC 50 values of isolates from the three populations collected in February showed that 80% of isolates from San Pablo and Coopecariari had EC 50 values greater than the highest EC 50 value from San Carlos, indicating a significant shift in reduced sensitivity to propiconazole. Isolates collected in November 1994, after eight treatments of propiconazole at San Pablo and Coopecariari, showed a significant increase in mean EC 50 values compared with the means observed in February. The high proportion of isolates with reduced sensitivity to propiconazole may account for the unsatisfactory control of black Sigatoka between 1992 and 1993 in the two banana plantations at San Pablo and Coopecariari.}, number={1}, journal={PHYTOPATHOLOGY}, author={Romero, RA and Sutton, TB}, year={1997}, month={Jan}, pages={96–100} }