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dc.creatorRupp, Thomases
dc.creatorOelschlägel, Birgites
dc.creatorBerjano Pérez, Reginaes
dc.creatorMahfoud, Hafezes
dc.creatorBuono, Danielees
dc.creatorWenke, Torstenes
dc.creatorRabitsch, Katharinaes
dc.creatorDötterl, Stefanes
dc.date.accessioned2024-06-07T15:51:11Z
dc.date.available2024-06-07T15:51:11Z
dc.date.issued2024-05
dc.identifier.citationRupp, T., Oelschlägel, B., Berjano Pérez, R., Mahfoud, H., Buono, D., Wenke, T.,...,Dötterl, S. (2024). Chemical imitation of yeast fermentation by the drosophilid-pollinated deceptive trap-flower Aristolochia baetica (Aristolochiaceae). Phytochemistry, 224, 114142. https://doi.org/10.1016/j.phytochem.2024.114142.
dc.identifier.issn0031-9422es
dc.identifier.issn1873-3700es
dc.identifier.urihttps://hdl.handle.net/11441/160116
dc.description.abstractDeceptive flowers, unlike in mutualistic pollination systems, mislead their pollinators by advertising rewards which ultimately are not provided. Although our understanding of deceptive pollination systems increased in recent years, the attractive signals and deceptive strategies in the majority of species remain unknown. This is also true for the genus Aristolochia, famous for its deceptive and fly-pollinated trap flowers. Representatives of this genus were generally assumed to be oviposition-site mimics, imitating vertebrate carrion or mushrooms. However, recent studies found a broader spectrum of strategies, including kleptomyiophily and imitation of invertebrate carrion. A different deceptive strategy is presented here for the western Mediterranean Aristolochia baetica L. We found that this species is mostly pollinated by drosophilid flies (Drosophilidae, mostly Drosophila spp.), which typically feed on fermenting fruit infested by yeasts. The flowers of A. baetica emitted mostly typical yeast volatiles, predominantly the aliphatic compounds acetoin and 2,3-butandiol, and derived acetates, as well as the aromatic compound 2-phenylethanol. Analyses of the absolute configurations of the chiral volatiles revealed weakly (acetoin, 2,3-butanediol) to strongly (mono- and diacetates) biased stereoisomer-ratios. Electrophysiological (GC-EAD) experiments and lab bioassays demonstrated that most of the floral volatiles, although not all stereoisomers of chiral compounds, were physiologically active and attractive in drosophilid pollinators; a synthetic mixture thereof successfully attracted them in field and lab bioassays. We conclude that A. baetica chemically mimics yeast fermentation to deceive its pollinators. This deceptive strategy (scent chemistry, pollinators, trapping function) is also known from more distantly related plants, such as Arum palaestinum Boiss. (Araceae) and Ceropegia spp. (Apocynaceae), suggesting convergent evolution. In contrast to other studies working on floral scents in plants imitating breeding sites, the present study considered the absolute configuration of chiral compounds.es
dc.description.sponsorshipAustrian Science Fund (FWF) 10.55776/I3722es
dc.description.sponsorshipGerman Research Foundation (DFG) WA 2461/9-1es
dc.formatapplication/pdfes
dc.format.extent14 p.es
dc.language.isoenges
dc.publisherElsevieres
dc.relation.ispartofPhytochemistry, 224, 114142.
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectAcetoines
dc.subjectAristolochia baeticaes
dc.subjectAristolochiaceaees
dc.subjectChemical mimicryes
dc.subjectDeceptive pollinationes
dc.subjectDrosophilidaees
dc.subjectElectroantennographyes
dc.subjectFloral scentses
dc.subjectPhoridaees
dc.subjectStereochemistryes
dc.titleChemical imitation of yeast fermentation by the drosophilid-pollinated deceptive trap-flower Aristolochia baetica (Aristolochiaceae)es
dc.typeinfo:eu-repo/semantics/articlees
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Biología Vegetal y Ecologíaes
dc.relation.projectID10.55776/I3722es
dc.relation.projectIDWA 2461/9-1es
dc.relation.publisherversionhttps://doi.org/10.1016/j.phytochem.2024.114142es
dc.identifier.doi10.1016/j.phytochem.2024.114142es
dc.journaltitlePhytochemistryes
dc.publication.volumen224es
dc.publication.initialPage114142es
dc.contributor.funderAustrian Science Fund (FWF)es
dc.contributor.funderDeutsche Forschungsgemeinschaft / German Research Foundation (DFG)es

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