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. 2020 Aug 11;11:4019. doi: 10.1038/s41467-020-17875-1

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© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — a Floral phenotype of a spring (left) and a summer (right) flower belonging to the same individual. Pictures were taken to the same individual in March and June 2018, respectively, in Malaha population (Granada province, Spain). b Average UV–Vis spectral reflectance of petals of spring (lilac line) and summer (grey line) flowers. Shaded area represents standard errors (n = 10 spring flowers and 10 summer flowers). c Phylomorphospace projection of the first three principal components of the corolla shape onto the phylogeny of the Brassiceae tribe (n = 72 species). It is shown the change in shape as deformation grids associated with extreme values of each component. The M. arvensis spring flower is shown as a large lilac dot and the M. arvensis summer flower as a large white dot. The Moricandia clade is shown in lilac.