dc.creatorNogueira, A.
dc.creatorRey, P. J.
dc.creatorLohmann, Lucia Garcez
dc.date.accessioned2013-10-14T17:09:53Z
dc.date.accessioned2018-07-04T15:58:18Z
dc.date.available2013-10-14T17:09:53Z
dc.date.available2018-07-04T15:58:18Z
dc.date.created2013-10-14T17:09:53Z
dc.date.issued2012
dc.identifierJOURNAL OF EVOLUTIONARY BIOLOGY, HOBOKEN, v. 25, n. 11, supl. 1, Part 2, pp. 2325-2340, NOV, 2012
dc.identifier1010-061X
dc.identifierhttp://www.producao.usp.br/handle/BDPI/34549
dc.identifier10.1111/j.1420-9101.2012.02615.x
dc.identifierhttp://dx.doi.org/10.1111/j.1420-9101.2012.02615.x
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1629887
dc.description.abstractMuch effort has been devoted to understanding the function of extrafloral nectaries (EFNs) for antplantherbivore interactions. However, the pattern of evolution of such structures throughout the history of plant lineages remains unexplored. In this study, we used empirical knowledge on plant defences mediated by ants as a theoretical framework to test specific hypotheses about the adaptive role of EFNs during plant evolution. Emphasis was given to different processes (neutral or adaptive) and factors (habitat change and trade-offs with new trichomes) that may have affected the evolution of antplant associations. We measured seven EFN quantitative traits in all 105 species included in a well-supported phylogeny of the tribe Bignonieae (Bignoniaceae) and collected field data on antEFN interactions in 32 species. We identified a positive association between ant visitation (a surrogate of ant guarding) and the abundance of EFNs in vegetative plant parts and rejected the hypothesis of phylogenetic conservatism of EFNs, with most traits presenting K-values < 1. Modelling the evolution of EFN traits using maximum likelihood approaches further suggested adaptive evolution, with static-optimum models showing a better fit than purely drift models. In addition, the abundance of EFNs was associated with habitat shifts (with a decrease in the abundance of EFNs from forest to savannas), and a potential trade-off was detected between the abundance of EFNs and estipitate glandular trichomes (i.e. trichomes with sticky secretion). These evolutionary associations suggest divergent selection between species as well as explains K-values < 1. Experimental studies with multiple lineages of forest and savanna taxa may improve our understanding of the role of nectaries in plants. Overall, our results suggest that the evolution of EFNs was likely associated with the adaptive process which probably played an important role in the diversification of this plant group.
dc.languageeng
dc.publisherWILEY-BLACKWELL
dc.publisherHOBOKEN
dc.relationJOURNAL OF EVOLUTIONARY BIOLOGY
dc.rightsCopyright WILEY-BLACKWELL
dc.rightsclosedAccess
dc.subjectADAPTATION
dc.subjectANT-PLANT INTERACTION
dc.subjectBRAZIL
dc.subjectCERRADO
dc.subjectDEFENCE TRAITS
dc.subjectEXTRAFLORAL NECTARIES
dc.subjectHERBIVORY
dc.subjectMACROEVOLUTION
dc.subjectPHYLOGENETIC SIGNAL
dc.subjectTRADE-OFF
dc.titleEvolution of extrafloral nectaries: adaptive process and selective regime changes from forest to savanna
dc.typeArtículos de revistas


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