Food quality effects on instar‐specific life histories of a holometabolous insect

Abstract It is a long‐standing challenge to understand how changes in food resources impact consumer life history traits and, in turn, impact how organisms interact with their environment. To characterize food quality effects on life history, most studies follow organisms throughout their life cycle...

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Autores principales: Leslie A. Holmes, William A. Nelson, Stephen C. Lougheed
Formato: article
Lenguaje:EN
Publicado: Wiley 2020
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spelling oai:doaj.org-article:dd92d71da4674956861914fa67d1e8262021-11-04T13:06:09ZFood quality effects on instar‐specific life histories of a holometabolous insect2045-775810.1002/ece3.5790https://doaj.org/article/dd92d71da4674956861914fa67d1e8262020-01-01T00:00:00Zhttps://doi.org/10.1002/ece3.5790https://doaj.org/toc/2045-7758Abstract It is a long‐standing challenge to understand how changes in food resources impact consumer life history traits and, in turn, impact how organisms interact with their environment. To characterize food quality effects on life history, most studies follow organisms throughout their life cycle and quantify major life events, such as age at maturity or fecundity. From these studies, we know that food quality generally impacts body size, juvenile development, and life span. Importantly, throughout juvenile development, many organisms develop through several stages of growth that can have different interactions with their environment. For example, some parasitoids typically attack larger instars, whereas larval insect predators typically attack smaller instars. Interestingly, most studies lump all juvenile stages together, which ignores these ecological changes over juvenile development. We combine a cross‐sectional experimental approach with a stage‐structured population model to estimate instar‐specific vital rates in the bean weevil, Callosobruchus maculatus across a food quality gradient. We characterize food quality effects on the bean weevil's life history traits throughout its juvenile ontogeny to test how food quality impacts instar‐specific vital rates. Vital rates differed across food quality treatments within each instar; however, their effect differed with instar. Weevils consuming low‐quality food spent 38%, 37%, and 18% more time, and were 34%, 53%, and 63% smaller than weevils consuming high‐quality food in the second, third, and fourth instars, respectively. Overall, our results show that consuming poor food quality means slower growth, but that food quality effects on vital rates, growth and development are not equal across instars. Differences in life history traits over juvenile ontogeny in response to food quality may impact how organisms interact with their environment, including how susceptible they are to predation, parasitism, and their competitive ability.Leslie A. HolmesWilliam A. NelsonStephen C. LougheedWileyarticlecowpea weeviljuvenile ontogenyphytophagous consumerstage‐structured population modelEcologyQH540-549.5ENEcology and Evolution, Vol 10, Iss 2, Pp 626-637 (2020)
institution DOAJ
collection DOAJ
language EN
topic cowpea weevil
juvenile ontogeny
phytophagous consumer
stage‐structured population model
Ecology
QH540-549.5
spellingShingle cowpea weevil
juvenile ontogeny
phytophagous consumer
stage‐structured population model
Ecology
QH540-549.5
Leslie A. Holmes
William A. Nelson
Stephen C. Lougheed
Food quality effects on instar‐specific life histories of a holometabolous insect
description Abstract It is a long‐standing challenge to understand how changes in food resources impact consumer life history traits and, in turn, impact how organisms interact with their environment. To characterize food quality effects on life history, most studies follow organisms throughout their life cycle and quantify major life events, such as age at maturity or fecundity. From these studies, we know that food quality generally impacts body size, juvenile development, and life span. Importantly, throughout juvenile development, many organisms develop through several stages of growth that can have different interactions with their environment. For example, some parasitoids typically attack larger instars, whereas larval insect predators typically attack smaller instars. Interestingly, most studies lump all juvenile stages together, which ignores these ecological changes over juvenile development. We combine a cross‐sectional experimental approach with a stage‐structured population model to estimate instar‐specific vital rates in the bean weevil, Callosobruchus maculatus across a food quality gradient. We characterize food quality effects on the bean weevil's life history traits throughout its juvenile ontogeny to test how food quality impacts instar‐specific vital rates. Vital rates differed across food quality treatments within each instar; however, their effect differed with instar. Weevils consuming low‐quality food spent 38%, 37%, and 18% more time, and were 34%, 53%, and 63% smaller than weevils consuming high‐quality food in the second, third, and fourth instars, respectively. Overall, our results show that consuming poor food quality means slower growth, but that food quality effects on vital rates, growth and development are not equal across instars. Differences in life history traits over juvenile ontogeny in response to food quality may impact how organisms interact with their environment, including how susceptible they are to predation, parasitism, and their competitive ability.
format article
author Leslie A. Holmes
William A. Nelson
Stephen C. Lougheed
author_facet Leslie A. Holmes
William A. Nelson
Stephen C. Lougheed
author_sort Leslie A. Holmes
title Food quality effects on instar‐specific life histories of a holometabolous insect
title_short Food quality effects on instar‐specific life histories of a holometabolous insect
title_full Food quality effects on instar‐specific life histories of a holometabolous insect
title_fullStr Food quality effects on instar‐specific life histories of a holometabolous insect
title_full_unstemmed Food quality effects on instar‐specific life histories of a holometabolous insect
title_sort food quality effects on instar‐specific life histories of a holometabolous insect
publisher Wiley
publishDate 2020
url https://doaj.org/article/dd92d71da4674956861914fa67d1e826
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