Behavioral responses of Diaphorina citri to host plant volatiles in multiple-choice olfactometers are affected in interpretable ways by effects of background colors and airflows

dc.contributor.affiliationInstituto Universitario Mixto de Biología Molecular y Celular de Plantas
dc.contributor.authorVolpe, H.X.L.es_ES
dc.contributor.authorZanardi, O.Z.es_ES
dc.contributor.authorMagnani, R.F.es_ES
dc.contributor.authorLuvizotto, R.A.G.es_ES
dc.contributor.authorEsperança, V.es_ES
dc.contributor.authorde Freitas, R.es_ES
dc.contributor.authorDelfino, J.Y.es_ES
dc.contributor.authorMulinari, T.A.es_ES
dc.contributor.authorCarvalho, R.I.es_ES
dc.contributor.authorWulff, N.A.es_ES
dc.contributor.authorde Miranda, M.P.es_ES
dc.contributor.authorPEÑA GARCIA, LEANDRO
dc.contributor.funderFundação de Amparo à Pesquisa do Estado de São Pauloes_ES
dc.date.accessioned2021-06-12T03:33:58Z
dc.date.available2021-06-12T03:33:58Z
dc.date.issued2020-07-06es_ES
dc.description.abstract[EN] In several phytophagous hemipterans, behavior appears to be mediated by both visual and chemical cues. For the Asian citrus psyllid (ACP)Diaphorina citri(Hemiptera: Liviidae), olfactometric assays are generally difficult to interpret owing to the low proportion of individuals responding to odors (similar to 30-40%), which compromises the efficiency and reliability of the results of behavioral tests. In the present study, the ACP behavioral response to emitted odors from sweet orange (Citrus sinensisL. Osbeck) flushes in a 4-arm olfactometer using different colors (four white-, two white- and two yellow- on opposite sides, or four yellow-colored fields), and the role of the airflow in the concentration of volatile organic compounds (VOCs) were assessed at two airflows [0.4 and 0.1 L/min (LPM)]. Exposure to 'Pera' sweet orange or clean air in treatments with four yellow-colored-fields increased the response rate of ACP females to the odor sources compared with exposure to 'Pera' sweet orange or clean air in treatments with four white-colored-fields, independently of the odor source and airflow tested. For the assays using two white- and two yellow-colored fields on opposite sides and 0.4 or 0.1 LPM airflow, the residence time of ACP females to odors ('Pera' sweet orange or clean air) was similar or higher in treatments using yellow- than those using white-colored fields. For both assays (VOCs and olfactometric behavioral parameters), the reduction in airflow from 0.4 to 0.1 LPM greatly changed the airborne concentration and ACP behavior. Quantitative chemical analyses revelead that the concentration of most compounds emitted by 'Pera' sweet orange flushes for the headspace using 0.1 LPM airflow were greater than the concentrations measured using 0.4 LPM airflow. Therefore, this treatment design provides an useful tool to assess the ACP behavioral response to the odors from citrus plants, and it can also help in the discrimination of dose-response screenings for VOCs or conspecific insects.en_EN
dc.description.accrualMethodSes_ES
dc.description.bibliographicCitationVolpe, H.; Zanardi, O.; Magnani, R.; Luvizotto, R.; Esperança, V.; De Freitas, R.; Delfino, J.... (2020). Behavioral responses of Diaphorina citri to host plant volatiles in multiple-choice olfactometers are affected in interpretable ways by effects of background colors and airflows. PLoS ONE. 15(7):1-17. https://doi.org/10.1371/journal.pone.0235630es_ES
dc.description.issue7es_ES
dc.description.referencesGrafton-Cardwell, E. E., Stelinski, L. L., & Stansly, P. A. (2013). Biology and Management of Asian Citrus Psyllid, Vector of the Huanglongbing Pathogens. Annual Review of Entomology, 58(1), 413-432. doi:10.1146/annurev-ento-120811-153542es_ES
dc.description.referencesTiwari, S., Mann, R. S., Rogers, M. E., & Stelinski, L. L. (2011). Insecticide resistance in field populations of Asian citrus psyllid in Florida. Pest Management Science, 67(10), 1258-1268. doi:10.1002/ps.2181es_ES
dc.description.referencesZanardi, O. Z., Bordini, G. P., Franco, A. A., de Morais, M. R., & Yamamoto, P. T. (2018). Spraying pyrethroid and neonicotinoid insecticides can induce outbreaks of Panonychus citri (Trombidiformes: Tetranychidae) in citrus groves. Experimental and Applied Acarology, 76(3), 339-354. doi:10.1007/s10493-018-0316-1es_ES
dc.description.referencesStockton, D. G., Martini, X., Patt, J. M., & Stelinski, L. L. (2016). The Influence of Learning on Host Plant Preference in a Significant Phytopathogen Vector, Diaphorina citri. PLOS ONE, 11(3), e0149815. doi:10.1371/journal.pone.0149815es_ES
dc.description.referencesKnolhoff, L. M., & Heckel, D. G. (2014). Behavioral Assays for Studies of Host Plant Choice and Adaptation in Herbivorous Insects. Annual Review of Entomology, 59(1), 263-278. doi:10.1146/annurev-ento-011613-161945es_ES
dc.description.referencesDöring, T. F., & Chittka, L. (2007). Visual ecology of aphids—a critical review on the role of colours in host finding. Arthropod-Plant Interactions, 1(1), 3-16. doi:10.1007/s11829-006-9000-1es_ES
dc.description.referencesNISSINEN, A., KRISTOFFERSEN, L., & ANDERBRANT, O. (2008). Physiological state of female and light intensity affect the host-plant selection of carrot psyllid, Trioza apicalis (Hemiptera: Triozidae). European Journal of Entomology, 105(2), 227-232. doi:10.14411/eje.2008.032es_ES
dc.description.referencesMOUND, L. A. (1962). STUDIES ON THE OLFACTION AND COLOUR SENSITIVITY OF BEMISIA TABACI (GENN.) (HOMOPTERA, ALEYRODIDAE). Entomologia Experimentalis et Applicata, 5(2), 99-104. doi:10.1111/j.1570-7458.1962.tb00571.xes_ES
dc.description.referencesAntignus, Y., Mor, N., Ben Joseph, R., Lapidot, M., & Cohen, S. (1996). Ultraviolet-Absorbing Plastic Sheets Protect Crops from Insect Pests and from Virus Diseases Vectored by Insects. Environmental Entomology, 25(5), 919-924. doi:10.1093/ee/25.5.919es_ES
dc.description.referencesHall, D. G., Sétamou, M., & Mizell, R. F. (2010). A comparison of sticky traps for monitoring Asian citrus psyllid (Diaphorina citri Kuwayama). Crop Protection, 29(11), 1341-1346. doi:10.1016/j.cropro.2010.06.003es_ES
dc.description.referencesGodfrey, K. E., Galindo, C., Patt, J. M., & Luque-Williams, M. (2013). Evaluation of Color and Scent Attractants Used to Trap and Detect Asian Ctirus Psyllid (Hemiptera: Liviidae) in Urban Environments. Florida Entomologist, 96(4), 1406-1416. doi:10.1653/024.096.0420es_ES
dc.description.referencesSétamou, M., Sanchez, A., Saldaña, R. R., Patt, J. M., & Summy, R. (2014). Visual Responses of Adult Asian Citrus Psyllid (Hemiptera: Liviidae) to Colored Sticky Traps on Citrus Trees. Journal of Insect Behavior, 27(4), 540-553. doi:10.1007/s10905-014-9448-2es_ES
dc.description.referencesMiranda, M. P., Dos Santos, F. L., Felippe, M. R., Moreno, A., & Fereres, A. (2015). Effect of UV-Blocking Plastic Films on Take-Off and Host Plant Finding Ability of Diaphorina citri (Hemiptera: Liviidae). Journal of Economic Entomology, 108(1), 245-251. doi:10.1093/jee/tou036es_ES
dc.description.referencesParis, T. M., Croxton, S. D., Stansly, P. A., & Allan, S. A. (2015). Temporal response and attraction ofDiaphorina citrito visual stimuli. Entomologia Experimentalis et Applicata, 155(2), 137-147. doi:10.1111/eea.12294es_ES
dc.description.referencesPatt, J. M., & Sétamou, M. (2010). Responses of the Asian Citrus Psyllid to Volatiles Emitted by the Flushing Shoots of Its Rutaceous Host Plants. Environmental Entomology, 39(2), 618-624. doi:10.1603/en09216es_ES
dc.description.referencesAmorós, M. E., Pereira das Neves, V., Rivas, F., Buenahora, J., Martini, X., Stelinski, L. L., & Rossini, C. (2018). Response of Diaphorina citri (Hemiptera: Liviidae) to volatiles characteristic of preferred citrus hosts. Arthropod-Plant Interactions, 13(3), 367-374. doi:10.1007/s11829-018-9651-8es_ES
dc.description.referencesGeorge, J., Shi, Q., Stelinski, L. L., Stover, E., & Lapointe, S. L. (2019). Host Selection, Oviposition and Feeding by a Phytopathogen Vector, Diaphorina citri (Hemiptera: Liviidae), Modulated by Plant Exposure to Formic Acid. Frontiers in Ecology and Evolution, 7. doi:10.3389/fevo.2019.00078es_ES
dc.description.referencesPettersson, J. (1970). An Aphid Sex Attractant. Insect Systematics & Evolution, 1(1), 63-73. doi:10.1163/187631270x00357es_ES
dc.description.referencesVET, L. E. M., LENTEREN, J. C. V., HEYMANS, M., & MEELIS, E. (1983). An airflow olfactometer for measuring olfactory responses of hymenopterous parasitoids and other small insects. Physiological Entomology, 8(1), 97-106. doi:10.1111/j.1365-3032.1983.tb00338.xes_ES
dc.description.referencesWenninger, E. J., Stelinski, L. L., & Hall, D. G. (2009). Roles of Olfactory Cues, Visual Cues, and Mating Status in Orientation of <I>Diaphorina citri</I> Kuwayama (Hemiptera: Psyllidae) to Four Different Host Plants. Environmental Entomology, 38(1), 225-234. doi:10.1603/022.038.0128es_ES
dc.description.referencesOnagbola, E. O., Rouseff, R. L., Smoot, J. M., & Stelinski, L. L. (2010). Guava leaf volatiles and dimethyl disulphide inhibit response of Diaphorina citri Kuwayama to host plant volatiles. Journal of Applied Entomology, 135(6), 404-414. doi:10.1111/j.1439-0418.2010.01565.xes_ES
dc.description.referencesAlquézar, B., Volpe, H. X. L., Magnani, R. F., de Miranda, M. P., Santos, M. A., Wulff, N. A., … Peña, L. (2017). β-caryophyllene emitted from a transgenic Arabidopsis or chemical dispenser repels Diaphorina citri, vector of Candidatus Liberibacters. Scientific Reports, 7(1). doi:10.1038/s41598-017-06119-wes_ES
dc.description.referencesTomaseto, A. F., Miranda, M. P., Moral, R. A., de Lara, I. A. R., Fereres, A., & Lopes, J. R. S. (2017). Environmental conditions for Diaphorina citri Kuwayama (Hemiptera: Liviidae) take-off. Journal of Applied Entomology, 142(1-2), 104-113. doi:10.1111/jen.12418es_ES
dc.description.referencesWenninger, E. J., & Hall, D. G. (2007). Daily Timing of Mating and Age at Reproductive Maturity in Diaphorina citri (Hemiptera: Psyllidae). Florida Entomologist, 90(4), 715-722. doi:10.1653/0015-4040(2007)90[715:dtomaa]2.0.co;2es_ES
dc.description.referencesShapiro, S. S., & Wilk, M. B. (1965). An Analysis of Variance Test for Normality (Complete Samples). Biometrika, 52(3/4), 591. doi:10.2307/2333709es_ES
dc.description.referencesNelder, J. A., & Wedderburn, R. W. M. (1972). Generalized Linear Models. Journal of the Royal Statistical Society. Series A (General), 135(3), 370. doi:10.2307/2344614es_ES
dc.description.referencesWilcoxon, F. (1945). Individual Comparisons by Ranking Methods. Biometrics Bulletin, 1(6), 80. doi:10.2307/3001968es_ES
dc.description.referencesPatt, J. M., Meikle, W. G., Mafra-Neto, A., Sétamou, M., Mangan, R., Yang, C., … Adamczyk, J. J. (2011). Multimodal Cues Drive Host-Plant Assessment in Asian Citrus Psyllid (Diaphorina citri). Environmental Entomology, 40(6), 1494-1502. doi:10.1603/en11149es_ES
dc.description.referencesTodd, J. W., Kays, S. J., & Kays, S. E. (1977). A precision low-flow-rate air delivery system for use with olfactometers. Journal of Chemical Ecology, 3(5), 519-525. doi:10.1007/bf00989073es_ES
dc.description.referencesBruce, T. J. A., Wadhams, L. J., & Woodcock, C. M. (2005). Insect host location: a volatile situation. Trends in Plant Science, 10(6), 269-274. doi:10.1016/j.tplants.2005.04.003es_ES
dc.description.referencesBruce, T. J. A., & Pickett, J. A. (2011). Perception of plant volatile blends by herbivorous insects – Finding the right mix. Phytochemistry, 72(13), 1605-1611. doi:10.1016/j.phytochem.2011.04.011es_ES
dc.description.sponsorshipFinancial support was provided by Sao Paulo Research Foundation (FAPESP) 2015/07011-3 and 2017/21460-0. The authors thank Dr. Aquidauana Miqueloto Zanardi for her help in measuring the color spaces of the white and yellow reflective papers used to change the device color.es_ES
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dc.identifier.doi10.1371/journal.pone.0235630es_ES
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dc.identifier.urihttps://riunet.upv.es/handle/10251/167871
dc.languageIngléses_ES
dc.publisherPublic Library of Sciencees_ES
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dc.relation.projectIDinfo:eu-repo/grantAgreement/FAPESP//2015%2F07011-3/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/FAPESP//2017%2F21460-0/es_ES
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pone.0235630es_ES
dc.relation.references10.1146/annurev-ento-120811-153542es_ES
dc.relation.references10.1002/ps.2181es_ES
dc.relation.references10.1007/s10493-018-0316-1es_ES
dc.relation.references10.1038/s41598-019-49469-3es_ES
dc.relation.references10.1007/s10886-018-0937-1es_ES
dc.relation.references10.1371/journal.pone.0149815es_ES
dc.relation.references10.1146/annurev-ento-011613-161945es_ES
dc.relation.references10.1007/s11829-006-9000-1es_ES
dc.relation.references10.14411/eje.2008.032es_ES
dc.relation.references10.1111/j.1570-7458.1962.tb00571.xes_ES
dc.relation.references10.1093/ee/25.5.919es_ES
dc.relation.references10.1016/j.cropro.2010.06.003es_ES
dc.relation.references10.1653/024.096.0420es_ES
dc.relation.references10.1007/s10905-014-9448-2es_ES
dc.relation.references10.1093/jee/tou036es_ES
dc.relation.references10.1111/eea.12294es_ES
dc.relation.references10.1603/EN09216es_ES
dc.relation.references10.1007/s11829-018-9651-8es_ES
dc.relation.references10.3389/fevo.2019.00078es_ES
dc.relation.references10.1163/187631270X00357es_ES
dc.relation.references10.1111/j.1365-3032.1983.tb00338.xes_ES
dc.relation.references10.1603/022.038.0128es_ES
dc.relation.references10.1111/j.1439-0418.2010.01565.xes_ES
dc.relation.references10.1038/s41598-017-06119-wes_ES
dc.relation.references10.1093/ee/nvx039es_ES
dc.relation.references10.1111/jen.12418es_ES
dc.relation.references10.3390/v8080225es_ES
dc.relation.references10.1653/0015-4040(2007)90[715:DTOMAA]2.0.CO;2es_ES
dc.relation.references10.2307/2333709es_ES
dc.relation.references10.2307/2344614es_ES
dc.relation.references10.2307/3001968es_ES
dc.relation.references10.1603/EN11149es_ES
dc.relation.references10.1007/BF00989073es_ES
dc.relation.references10.1016/j.tplants.2005.04.003es_ES
dc.relation.references10.1016/j.phytochem.2011.04.011es_ES
dc.relation.references10.1016/j.jplph.2016.11.001es_ES
dc.relation.references10.1038/s41598-019-38597-5es_ES
dc.rightsReconocimiento (by)es_ES
dc.rights.accessRightsAbiertoes_ES
dc.subjectPsyllid Hemiptera Liviidaees_ES
dc.subjectSticky trapses_ES
dc.subjectKuwayamaes_ES
dc.subjectCueses_ES
dc.titleBehavioral responses of Diaphorina citri to host plant volatiles in multiple-choice olfactometers are affected in interpretable ways by effects of background colors and airflowses_ES
dc.typeArtículoes_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
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