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Evolution of extreme proboscis lengths in Neotropical Hesperiidae (Lepidoptera)

Exaggerated morphologies have evolved in insects as adaptations to nectar feeding by natural selection. For example, the suctorial mouthparts of butterflies enable these insects to gain access to floral nectar concealed inside deep floral tubes. Proboscis length in Lepidoptera is known to scale with...

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Autores principales: Bauder, J. A.-S., Warren, A. D., Krenn, H. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412924/
https://www.ncbi.nlm.nih.gov/pubmed/25937673
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author Bauder, J. A.-S.
Warren, A. D.
Krenn, H. W.
author_facet Bauder, J. A.-S.
Warren, A. D.
Krenn, H. W.
author_sort Bauder, J. A.-S.
collection PubMed
description Exaggerated morphologies have evolved in insects as adaptations to nectar feeding by natural selection. For example, the suctorial mouthparts of butterflies enable these insects to gain access to floral nectar concealed inside deep floral tubes. Proboscis length in Lepidoptera is known to scale with body size, but whether extreme absolute proboscis lengths of nectar feeding butterflies result from a proportional or disproportional increase with body size that differs between phylogenetic lineages remains unknown. We surveyed the range of variation that occurs in scaling relationships between proboscis length and body size against a phylogenetic background among Costa Rican Hesperiidae. We obtained a new record holder for the longest proboscis in butterflies and showed that extremely long proboscides evolved at least three times independently within Neotropical Hesperiidae. We conclude that the evolution of extremely long proboscides results from allometric scaling with body size, as demonstrated in hawk moths. We hypothesize that constraints on the evolution of increasingly long butterfly proboscides may come from (1) the underlying scaling relationships, i.e., relative proboscis length, combined with the butterfly’s flight style and flower-visiting behaviour and/or (2) developmental constraints during the pupal phase. Lastly, we discuss why butterflies did not evolve similar scaling relationships as hawk moths.
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spelling pubmed-44129242015-04-29 Evolution of extreme proboscis lengths in Neotropical Hesperiidae (Lepidoptera) Bauder, J. A.-S. Warren, A. D. Krenn, H. W. J Res Lepid Article Exaggerated morphologies have evolved in insects as adaptations to nectar feeding by natural selection. For example, the suctorial mouthparts of butterflies enable these insects to gain access to floral nectar concealed inside deep floral tubes. Proboscis length in Lepidoptera is known to scale with body size, but whether extreme absolute proboscis lengths of nectar feeding butterflies result from a proportional or disproportional increase with body size that differs between phylogenetic lineages remains unknown. We surveyed the range of variation that occurs in scaling relationships between proboscis length and body size against a phylogenetic background among Costa Rican Hesperiidae. We obtained a new record holder for the longest proboscis in butterflies and showed that extremely long proboscides evolved at least three times independently within Neotropical Hesperiidae. We conclude that the evolution of extremely long proboscides results from allometric scaling with body size, as demonstrated in hawk moths. We hypothesize that constraints on the evolution of increasingly long butterfly proboscides may come from (1) the underlying scaling relationships, i.e., relative proboscis length, combined with the butterfly’s flight style and flower-visiting behaviour and/or (2) developmental constraints during the pupal phase. Lastly, we discuss why butterflies did not evolve similar scaling relationships as hawk moths. 2014-12-01 /pmc/articles/PMC4412924/ /pubmed/25937673 Text en Copyright: This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ or send a letter to Creative Commons, 171 Second Street, Suite 300, San Francisco, California, 94105, USA.
spellingShingle Article
Bauder, J. A.-S.
Warren, A. D.
Krenn, H. W.
Evolution of extreme proboscis lengths in Neotropical Hesperiidae (Lepidoptera)
title Evolution of extreme proboscis lengths in Neotropical Hesperiidae (Lepidoptera)
title_full Evolution of extreme proboscis lengths in Neotropical Hesperiidae (Lepidoptera)
title_fullStr Evolution of extreme proboscis lengths in Neotropical Hesperiidae (Lepidoptera)
title_full_unstemmed Evolution of extreme proboscis lengths in Neotropical Hesperiidae (Lepidoptera)
title_short Evolution of extreme proboscis lengths in Neotropical Hesperiidae (Lepidoptera)
title_sort evolution of extreme proboscis lengths in neotropical hesperiidae (lepidoptera)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412924/
https://www.ncbi.nlm.nih.gov/pubmed/25937673
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