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Evolution of Specialization of Cassida rubiginosa on Cirsium arvense (Compositae, Cardueae)

The majority of herbivorous insects are specialized feeders restricted to a plant family, genus, or species. The evolution of specialized insect–plant interactions is generally considered to be a result of trade-offs in fitness between possible hosts. Through the course of natural selection, host pl...

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Autores principales: Cripps, Michael G., Jackman, Sarah D., Roquet, Cristina, van Koten, Chikako, Rostás, Michael, Bourdôt, Graeme W., Susanna, Alfonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994537/
https://www.ncbi.nlm.nih.gov/pubmed/27602042
http://dx.doi.org/10.3389/fpls.2016.01261
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author Cripps, Michael G.
Jackman, Sarah D.
Roquet, Cristina
van Koten, Chikako
Rostás, Michael
Bourdôt, Graeme W.
Susanna, Alfonso
author_facet Cripps, Michael G.
Jackman, Sarah D.
Roquet, Cristina
van Koten, Chikako
Rostás, Michael
Bourdôt, Graeme W.
Susanna, Alfonso
author_sort Cripps, Michael G.
collection PubMed
description The majority of herbivorous insects are specialized feeders restricted to a plant family, genus, or species. The evolution of specialized insect–plant interactions is generally considered to be a result of trade-offs in fitness between possible hosts. Through the course of natural selection, host plants that maximize insect fitness should result in optimal, specialized, insect–plant associations. However, the extent to which insects are tracking plant phylogeny or key plant traits that act as herbivore resistance or acceptance characters is uncertain. Thus, with regard to the evolution of host plant specialization, we tested if insect performance is explained by phylogenetic relatedness of potential host plants, or key plant traits that are not phylogenetically related. We tested the survival (naive first instar to adult) of the oligophagous leaf-feeding beetle, Cassida rubiginosa, on 16 selected representatives of the Cardueae tribe (thistles and knapweeds), including some of the worst weeds in temperate grasslands of the world in terms of the economic impacts caused by lost productivity. Leaf traits (specific leaf area, leaf pubescence, flavonoid concentration, carbon and nitrogen content) were measured as explanatory variables and tested in relation to survival of the beetle, and the phylogenetic signal of the traits were examined. The survival of C. rubiginosa decreased with increasing phylogenetic distance from the known primary host plant, C. arvense, suggesting that specialization is a conserved character, and that insect host range, to a large degree is constrained by evolutionary history. The only trait measured that clearly offered some explanatory value for the survival of C. rubiginosa was specific leaf area. This trait was not phylogenetically dependant, and when combined with phylogenetic distance from C. arvense gave the best model explaining C. rubiginosa survival. We conclude that the specialization of the beetle is explained by a combination of adaptation to an optimal host plant over evolutionary time, and key plant traits such as specific leaf area that can restrict or broaden host utilization within the Cardueae lineage. The phylogenetic pattern of C. rubiginosa fitness will aid in predicting the ability of this biocontrol agent to control multiple Cardueae weeds.
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spelling pubmed-49945372016-09-06 Evolution of Specialization of Cassida rubiginosa on Cirsium arvense (Compositae, Cardueae) Cripps, Michael G. Jackman, Sarah D. Roquet, Cristina van Koten, Chikako Rostás, Michael Bourdôt, Graeme W. Susanna, Alfonso Front Plant Sci Plant Science The majority of herbivorous insects are specialized feeders restricted to a plant family, genus, or species. The evolution of specialized insect–plant interactions is generally considered to be a result of trade-offs in fitness between possible hosts. Through the course of natural selection, host plants that maximize insect fitness should result in optimal, specialized, insect–plant associations. However, the extent to which insects are tracking plant phylogeny or key plant traits that act as herbivore resistance or acceptance characters is uncertain. Thus, with regard to the evolution of host plant specialization, we tested if insect performance is explained by phylogenetic relatedness of potential host plants, or key plant traits that are not phylogenetically related. We tested the survival (naive first instar to adult) of the oligophagous leaf-feeding beetle, Cassida rubiginosa, on 16 selected representatives of the Cardueae tribe (thistles and knapweeds), including some of the worst weeds in temperate grasslands of the world in terms of the economic impacts caused by lost productivity. Leaf traits (specific leaf area, leaf pubescence, flavonoid concentration, carbon and nitrogen content) were measured as explanatory variables and tested in relation to survival of the beetle, and the phylogenetic signal of the traits were examined. The survival of C. rubiginosa decreased with increasing phylogenetic distance from the known primary host plant, C. arvense, suggesting that specialization is a conserved character, and that insect host range, to a large degree is constrained by evolutionary history. The only trait measured that clearly offered some explanatory value for the survival of C. rubiginosa was specific leaf area. This trait was not phylogenetically dependant, and when combined with phylogenetic distance from C. arvense gave the best model explaining C. rubiginosa survival. We conclude that the specialization of the beetle is explained by a combination of adaptation to an optimal host plant over evolutionary time, and key plant traits such as specific leaf area that can restrict or broaden host utilization within the Cardueae lineage. The phylogenetic pattern of C. rubiginosa fitness will aid in predicting the ability of this biocontrol agent to control multiple Cardueae weeds. Frontiers Media S.A. 2016-08-23 /pmc/articles/PMC4994537/ /pubmed/27602042 http://dx.doi.org/10.3389/fpls.2016.01261 Text en Copyright © 2016 Cripps, Jackman, Roquet, van Koten, Rostás, Bourdôt and Susanna. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Cripps, Michael G.
Jackman, Sarah D.
Roquet, Cristina
van Koten, Chikako
Rostás, Michael
Bourdôt, Graeme W.
Susanna, Alfonso
Evolution of Specialization of Cassida rubiginosa on Cirsium arvense (Compositae, Cardueae)
title Evolution of Specialization of Cassida rubiginosa on Cirsium arvense (Compositae, Cardueae)
title_full Evolution of Specialization of Cassida rubiginosa on Cirsium arvense (Compositae, Cardueae)
title_fullStr Evolution of Specialization of Cassida rubiginosa on Cirsium arvense (Compositae, Cardueae)
title_full_unstemmed Evolution of Specialization of Cassida rubiginosa on Cirsium arvense (Compositae, Cardueae)
title_short Evolution of Specialization of Cassida rubiginosa on Cirsium arvense (Compositae, Cardueae)
title_sort evolution of specialization of cassida rubiginosa on cirsium arvense (compositae, cardueae)
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994537/
https://www.ncbi.nlm.nih.gov/pubmed/27602042
http://dx.doi.org/10.3389/fpls.2016.01261
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