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The evolution of adult pollen feeding did not alter postembryonic growth in Heliconius butterflies
For many animals, the availability and provision of dietary resources can vary markedly between juvenile and adult stages, often leading to a temporal separation of nutrient acquisition and use. Juvenile developmental programs are likely limited by the energetic demands of many adult tissues and pro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237422/ https://www.ncbi.nlm.nih.gov/pubmed/35784071 http://dx.doi.org/10.1002/ece3.8999 |
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author | Hebberecht, Laura Melo‐Flórez, Lina Young, Fletcher J. McMillan, W. Owen Montgomery, Stephen H. |
author_facet | Hebberecht, Laura Melo‐Flórez, Lina Young, Fletcher J. McMillan, W. Owen Montgomery, Stephen H. |
author_sort | Hebberecht, Laura |
collection | PubMed |
description | For many animals, the availability and provision of dietary resources can vary markedly between juvenile and adult stages, often leading to a temporal separation of nutrient acquisition and use. Juvenile developmental programs are likely limited by the energetic demands of many adult tissues and processes with early developmental origins. Enhanced dietary quality in the adult stage may, therefore, alter selection on life history and growth patterns in juvenile stages. Heliconius are unique among butterflies in actively collecting and digesting pollen grains, which provide an adult source of essential amino acids. The origin of pollen feeding has therefore previously been hypothesized to lift constraints on larval growth rates, allowing Heliconius to spend less time as larvae when they are most vulnerable to predation. By measuring larval and pupal life‐history traits across three pollen‐feeding and three nonpollen‐feeding Heliconiini, we provide the first test of this hypothesis. Although we detect significant interspecific variation in larval and pupal development, we do not find any consistent shift associated with pollen feeding. We discuss how this result may fit with patterns of nitrogen allocation, the benefits of nitrogenous stores, and developmental limitations on growth. Our results provide a framework for studies aiming to link innovations in adult Heliconius to altered selection regimes and developmental programs in early life stages. |
format | Online Article Text |
id | pubmed-9237422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92374222022-07-01 The evolution of adult pollen feeding did not alter postembryonic growth in Heliconius butterflies Hebberecht, Laura Melo‐Flórez, Lina Young, Fletcher J. McMillan, W. Owen Montgomery, Stephen H. Ecol Evol Research Articles For many animals, the availability and provision of dietary resources can vary markedly between juvenile and adult stages, often leading to a temporal separation of nutrient acquisition and use. Juvenile developmental programs are likely limited by the energetic demands of many adult tissues and processes with early developmental origins. Enhanced dietary quality in the adult stage may, therefore, alter selection on life history and growth patterns in juvenile stages. Heliconius are unique among butterflies in actively collecting and digesting pollen grains, which provide an adult source of essential amino acids. The origin of pollen feeding has therefore previously been hypothesized to lift constraints on larval growth rates, allowing Heliconius to spend less time as larvae when they are most vulnerable to predation. By measuring larval and pupal life‐history traits across three pollen‐feeding and three nonpollen‐feeding Heliconiini, we provide the first test of this hypothesis. Although we detect significant interspecific variation in larval and pupal development, we do not find any consistent shift associated with pollen feeding. We discuss how this result may fit with patterns of nitrogen allocation, the benefits of nitrogenous stores, and developmental limitations on growth. Our results provide a framework for studies aiming to link innovations in adult Heliconius to altered selection regimes and developmental programs in early life stages. John Wiley and Sons Inc. 2022-06-27 /pmc/articles/PMC9237422/ /pubmed/35784071 http://dx.doi.org/10.1002/ece3.8999 Text en © 2022 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Articles Hebberecht, Laura Melo‐Flórez, Lina Young, Fletcher J. McMillan, W. Owen Montgomery, Stephen H. The evolution of adult pollen feeding did not alter postembryonic growth in Heliconius butterflies |
title | The evolution of adult pollen feeding did not alter postembryonic growth in Heliconius butterflies |
title_full | The evolution of adult pollen feeding did not alter postembryonic growth in Heliconius butterflies |
title_fullStr | The evolution of adult pollen feeding did not alter postembryonic growth in Heliconius butterflies |
title_full_unstemmed | The evolution of adult pollen feeding did not alter postembryonic growth in Heliconius butterflies |
title_short | The evolution of adult pollen feeding did not alter postembryonic growth in Heliconius butterflies |
title_sort | evolution of adult pollen feeding did not alter postembryonic growth in heliconius butterflies |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237422/ https://www.ncbi.nlm.nih.gov/pubmed/35784071 http://dx.doi.org/10.1002/ece3.8999 |
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