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Beyond buzz‐pollination – departures from an adaptive plateau lead to new pollination syndromes

Pollination syndromes describe recurring adaptation to selection imposed by distinct pollinators. We tested for pollination syndromes in Merianieae (Melastomataceae), which contain bee‐ (buzz‐), hummingbird‐, flowerpiercer‐, passerine‐, bat‐ and rodent‐pollinated species. Further, we explored trait...

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Autores principales: Dellinger, Agnes S., Chartier, Marion, Fernández‐Fernández, Diana, Penneys, Darin S., Alvear, Marcela, Almeda, Frank, Michelangeli, Fabián A., Staedler, Yannick, Armbruster, W. Scott, Schönenberger, Jürg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492237/
https://www.ncbi.nlm.nih.gov/pubmed/30368819
http://dx.doi.org/10.1111/nph.15468
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author Dellinger, Agnes S.
Chartier, Marion
Fernández‐Fernández, Diana
Penneys, Darin S.
Alvear, Marcela
Almeda, Frank
Michelangeli, Fabián A.
Staedler, Yannick
Armbruster, W. Scott
Schönenberger, Jürg
author_facet Dellinger, Agnes S.
Chartier, Marion
Fernández‐Fernández, Diana
Penneys, Darin S.
Alvear, Marcela
Almeda, Frank
Michelangeli, Fabián A.
Staedler, Yannick
Armbruster, W. Scott
Schönenberger, Jürg
author_sort Dellinger, Agnes S.
collection PubMed
description Pollination syndromes describe recurring adaptation to selection imposed by distinct pollinators. We tested for pollination syndromes in Merianieae (Melastomataceae), which contain bee‐ (buzz‐), hummingbird‐, flowerpiercer‐, passerine‐, bat‐ and rodent‐pollinated species. Further, we explored trait changes correlated with the repeated shifts away from buzz‐pollination, which represents an ‘adaptive plateau’ in Melastomataceae. We used random forest analyses to identify key traits associated with the different pollinators of 19 Merianieae species and estimated the pollination syndromes of 42 more species. We employed morphospace analyses to compare the morphological diversity (disparity) among syndromes. We identified three pollination syndromes (‘buzz‐bee’, ‘mixed‐vertebrate’ and ‘passerine’), characterized by different pollen expulsion mechanisms and reward types, but not by traditional syndrome characters. Further, we found that ‘efficiency’ rather than ‘attraction’ traits were important for syndrome circumscription. Contrary to syndrome theory, our study supports the pooling of different pollinators (hummingbirds, bats, rodents and flowerpiercers) into the ‘mixed‐vertebrate’ syndrome, and we found that disparity was highest in the ‘buzz‐bee’ syndrome. We conclude that the highly adaptive buzz‐pollination system may have prevented shifts towards classical pollination syndromes, but provided the starting point for the evolution of a novel set of distinct syndromes, all having retained multifunctional stamens that provide pollen expulsion, reward and attraction.
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spelling pubmed-64922372019-05-07 Beyond buzz‐pollination – departures from an adaptive plateau lead to new pollination syndromes Dellinger, Agnes S. Chartier, Marion Fernández‐Fernández, Diana Penneys, Darin S. Alvear, Marcela Almeda, Frank Michelangeli, Fabián A. Staedler, Yannick Armbruster, W. Scott Schönenberger, Jürg New Phytol Research Pollination syndromes describe recurring adaptation to selection imposed by distinct pollinators. We tested for pollination syndromes in Merianieae (Melastomataceae), which contain bee‐ (buzz‐), hummingbird‐, flowerpiercer‐, passerine‐, bat‐ and rodent‐pollinated species. Further, we explored trait changes correlated with the repeated shifts away from buzz‐pollination, which represents an ‘adaptive plateau’ in Melastomataceae. We used random forest analyses to identify key traits associated with the different pollinators of 19 Merianieae species and estimated the pollination syndromes of 42 more species. We employed morphospace analyses to compare the morphological diversity (disparity) among syndromes. We identified three pollination syndromes (‘buzz‐bee’, ‘mixed‐vertebrate’ and ‘passerine’), characterized by different pollen expulsion mechanisms and reward types, but not by traditional syndrome characters. Further, we found that ‘efficiency’ rather than ‘attraction’ traits were important for syndrome circumscription. Contrary to syndrome theory, our study supports the pooling of different pollinators (hummingbirds, bats, rodents and flowerpiercers) into the ‘mixed‐vertebrate’ syndrome, and we found that disparity was highest in the ‘buzz‐bee’ syndrome. We conclude that the highly adaptive buzz‐pollination system may have prevented shifts towards classical pollination syndromes, but provided the starting point for the evolution of a novel set of distinct syndromes, all having retained multifunctional stamens that provide pollen expulsion, reward and attraction. John Wiley and Sons Inc. 2018-10-12 2019-01 /pmc/articles/PMC6492237/ /pubmed/30368819 http://dx.doi.org/10.1111/nph.15468 Text en © 2018 The Authors. New Phytologist © 2018 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Dellinger, Agnes S.
Chartier, Marion
Fernández‐Fernández, Diana
Penneys, Darin S.
Alvear, Marcela
Almeda, Frank
Michelangeli, Fabián A.
Staedler, Yannick
Armbruster, W. Scott
Schönenberger, Jürg
Beyond buzz‐pollination – departures from an adaptive plateau lead to new pollination syndromes
title Beyond buzz‐pollination – departures from an adaptive plateau lead to new pollination syndromes
title_full Beyond buzz‐pollination – departures from an adaptive plateau lead to new pollination syndromes
title_fullStr Beyond buzz‐pollination – departures from an adaptive plateau lead to new pollination syndromes
title_full_unstemmed Beyond buzz‐pollination – departures from an adaptive plateau lead to new pollination syndromes
title_short Beyond buzz‐pollination – departures from an adaptive plateau lead to new pollination syndromes
title_sort beyond buzz‐pollination – departures from an adaptive plateau lead to new pollination syndromes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492237/
https://www.ncbi.nlm.nih.gov/pubmed/30368819
http://dx.doi.org/10.1111/nph.15468
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