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      Anther cones increase pollen release in buzz‐pollinated Solanum flowers

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          Abstract

          The widespread evolution of tube‐like anthers releasing pollen from apical pores is associated with buzz pollination, in which bees vibrate flowers to remove pollen. The mechanical connection among anthers in buzz‐pollinated species varies from loosely held conformations, to anthers tightly held together with trichomes or bioadhesives forming a functionally joined conical structure (anther cone). Joined anther cones in buzz‐pollinated species have evolved independently across plant families and via different genetic mechanisms, yet their functional significance remains mostly untested. We used experimental manipulations to compare vibrational and functional (pollen release) consequences of joined anther cones in three buzz‐pollinated species of Solanum (Solanaceae). We applied bee‐like vibrations to focal anthers in flowers with (“joined”) and without (“free”) experimentally created joined anther cones, and characterized vibrations transmitted to other anthers and the amount of pollen released. We found that joined anther architectures cause nonfocal anthers to vibrate at higher amplitudes than free architectures. Moreover, in the two species with naturally loosely held anthers, anther fusion increases pollen release, whereas in the species with a free but naturally compact architecture it does not. We discuss hypotheses for the adaptive significance of the convergent evolution of joined anther cones.

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              A phylogenetic framework for evolutionary study of the nightshades (Solanaceae): a dated 1000-tip tree

              Background The Solanaceae is a plant family of great economic importance. Despite a wealth of phylogenetic work on individual clades and a deep knowledge of particular cultivated species such as tomato and potato, a robust evolutionary framework with a dated molecular phylogeny for the family is still lacking. Here we investigate molecular divergence times for Solanaceae using a densely-sampled species-level phylogeny. We also review the fossil record of the family to derive robust calibration points, and estimate a chronogram using an uncorrelated relaxed molecular clock. Results Our densely-sampled phylogeny shows strong support for all previously identified clades of Solanaceae and strongly supported relationships between the major clades, particularly within Solanum. The Tomato clade is shown to be sister to section Petota, and the Regmandra clade is the first branching member of the Potato clade. The minimum age estimates for major splits within the family provided here correspond well with results from previous studies, indicating splits between tomato & potato around 8 Million years ago (Ma) with a 95% highest posterior density (HPD) 7–10 Ma, Solanum & Capsicum c. 19 Ma (95% HPD 17–21), and Solanum & Nicotiana c. 24 Ma (95% HPD 23–26). Conclusions Our large time-calibrated phylogeny provides a significant step towards completing a fully sampled species-level phylogeny for Solanaceae, and provides age estimates for the whole family. The chronogram now includes 40% of known species and all but two monotypic genera, and is one of the best sampled angiosperm family phylogenies both in terms of taxon sampling and resolution published thus far. The increased resolution in the chronogram combined with the large increase in species sampling will provide much needed data for the examination of many biological questions using Solanaceae as a model system.
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                Author and article information

                Contributors
                mario.vallejo@stir.ac.uk
                Journal
                Evolution
                Evolution
                10.1111/(ISSN)1558-5646
                EVO
                Evolution; International Journal of Organic Evolution
                John Wiley and Sons Inc. (Hoboken )
                0014-3820
                1558-5646
                31 March 2022
                May 2022
                : 76
                : 5 ( doiID: 10.1111/evo.v76.5 )
                : 931-945
                Affiliations
                [ 1 ] Biological and Environmental Sciences University of Stirling Stirling FK9 4LA United Kingdom
                [ 2 ] Department of Biology Missouri State University Springfield Missouri 65897
                Author notes
                Author information
                https://orcid.org/0000-0002-5663-8025
                https://orcid.org/0000-0002-7534-0697
                https://orcid.org/0000-0001-8036-2711
                Article
                EVO14485
                10.1111/evo.14485
                9313847
                35324004
                8b59a755-7698-432a-9323-762203a0982b
                © 2022 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 21 February 2022
                : 02 October 2021
                : 13 March 2022
                Page count
                Figures: 6, Tables: 3, Pages: 15, Words: 9314
                Funding
                Funded by: Leverhulme Trust , doi 10.13039/501100000275;
                Award ID: RPG‐2018‐235
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                May 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.7 mode:remove_FC converted:25.07.2022

                Evolutionary Biology
                anther cone,bees,buzz pollination,convergent evolution,pollen release,pollination
                Evolutionary Biology
                anther cone, bees, buzz pollination, convergent evolution, pollen release, pollination

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