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Herbivory as an important selective force in the evolution of floral traits and pollinator shifts

Floral trait evolution is frequently attributed to pollinator-mediated selection but herbivores can play a key role in shaping plant reproductive biology. Here we examine the role of florivores in driving floral trait evolution and pollinator shifts in a recently radiated clade of flowering plants,...

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Autores principales: Jogesh, Tania, Overson, Rick P., Raguso, Robert A., Skogen, Krissa A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499749/
https://www.ncbi.nlm.nih.gov/pubmed/28011456
http://dx.doi.org/10.1093/aobpla/plw088
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author Jogesh, Tania
Overson, Rick P.
Raguso, Robert A.
Skogen, Krissa A.
author_facet Jogesh, Tania
Overson, Rick P.
Raguso, Robert A.
Skogen, Krissa A.
author_sort Jogesh, Tania
collection PubMed
description Floral trait evolution is frequently attributed to pollinator-mediated selection but herbivores can play a key role in shaping plant reproductive biology. Here we examine the role of florivores in driving floral trait evolution and pollinator shifts in a recently radiated clade of flowering plants, Oenothera sect. Calylophus. We compare florivory by a specialist, internal feeder, Mompha, on closely related hawkmoth- and bee-pollinated species and document variation in damage based on floral traits within sites, species and among species. Our results show that flowers with longer floral tubes and decreased floral flare have increased Mompha damage. Bee-pollinated flowers, which have substantially smaller floral tubes, experience on average 13% less Mompha florivory than do hawkmoth-pollinated flowers. The positive association between tube length and Mompha damage is evident even within sites of some species, suggesting that Mompha can drive trait differentiation at microevolutionary scales. Given that there are at least two independent shifts from hawkmoth to bee pollination in this clade, florivore-mediated selection on floral traits may have played an important role in facilitating morphological changes associated with transitions from hawkmoth to bee pollination.
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spelling pubmed-54997492017-07-12 Herbivory as an important selective force in the evolution of floral traits and pollinator shifts Jogesh, Tania Overson, Rick P. Raguso, Robert A. Skogen, Krissa A. AoB Plants Using Non-Model Systems to Explore Plant–Pollinator and Plant–Herbivore Interactions Floral trait evolution is frequently attributed to pollinator-mediated selection but herbivores can play a key role in shaping plant reproductive biology. Here we examine the role of florivores in driving floral trait evolution and pollinator shifts in a recently radiated clade of flowering plants, Oenothera sect. Calylophus. We compare florivory by a specialist, internal feeder, Mompha, on closely related hawkmoth- and bee-pollinated species and document variation in damage based on floral traits within sites, species and among species. Our results show that flowers with longer floral tubes and decreased floral flare have increased Mompha damage. Bee-pollinated flowers, which have substantially smaller floral tubes, experience on average 13% less Mompha florivory than do hawkmoth-pollinated flowers. The positive association between tube length and Mompha damage is evident even within sites of some species, suggesting that Mompha can drive trait differentiation at microevolutionary scales. Given that there are at least two independent shifts from hawkmoth to bee pollination in this clade, florivore-mediated selection on floral traits may have played an important role in facilitating morphological changes associated with transitions from hawkmoth to bee pollination. Oxford University Press 2016-12-22 /pmc/articles/PMC5499749/ /pubmed/28011456 http://dx.doi.org/10.1093/aobpla/plw088 Text en © The Authors 2016. Published by Oxford University Press on behalf of the Annals of Botany Company. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Using Non-Model Systems to Explore Plant–Pollinator and Plant–Herbivore Interactions
Jogesh, Tania
Overson, Rick P.
Raguso, Robert A.
Skogen, Krissa A.
Herbivory as an important selective force in the evolution of floral traits and pollinator shifts
title Herbivory as an important selective force in the evolution of floral traits and pollinator shifts
title_full Herbivory as an important selective force in the evolution of floral traits and pollinator shifts
title_fullStr Herbivory as an important selective force in the evolution of floral traits and pollinator shifts
title_full_unstemmed Herbivory as an important selective force in the evolution of floral traits and pollinator shifts
title_short Herbivory as an important selective force in the evolution of floral traits and pollinator shifts
title_sort herbivory as an important selective force in the evolution of floral traits and pollinator shifts
topic Using Non-Model Systems to Explore Plant–Pollinator and Plant–Herbivore Interactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499749/
https://www.ncbi.nlm.nih.gov/pubmed/28011456
http://dx.doi.org/10.1093/aobpla/plw088
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