Literature DB >> 29592544

Specialized Feeding Behavior Influences Both Ecological Specialization and Assortative Mating in Sympatric Host Races of Pea Aphids.

Marina C Caillaud, Sara Via.   

Abstract

Not only is ecological specialization a defining feature of much of Earth's biological diversity, the evolution of specialization may also play a central role in generating diversity by facilitating speciation. To understand how ecological specialization evolves, we must know the particular characters that cause organisms to be specialized. For example, most theories of specialization in herbivorous insects emphasize physiological trade-offs in response to toxic plant chemicals. However, even in herbivores, it is likely that other characters are also involved in resource specialization. Knowing the causes of ecological specialization is also crucial for linking specialization to speciation. When the same character(s) that cause specialization also influence assortative mating, speciation may occur particularly rapidly because specialization and reproductive isolation become coupled in a positive feedback that speeds the evolution of both. Indeed, a central hypothesis in the study of ecological speciation is that specialization in recently diverged taxa may often be due to characters that also produce assortative mating. We test this hypothesis by evaluating the causes of ecological specialization among host-associated populations of an herbivorous insect, the pea aphid (Acyrthosiphon pisum). These populations are highly specialized on different host plants (alfalfa or clover; "alternate hosts"), and the races are partially reproductively isolated. Here, we identify key characters responsible for host plant specialization. Our results suggest that the major proximal determinant of host specialization is the behavioral acceptance of a plant rather than the toxicity of the food source. Pea aphids rapidly assess alfalfa and clover and reject the alternate host based on chemical cues that are perceived before the initiation of feeding. This rapid behavioral rejection of the alternate host by a given race has two consequences. First, unrestrained aphids quickly leave the alternate host and search for other plants. Because pea aphids mate on their host plants, divergence in host acceptance among ecologically specialized races leads to congregation on the favored host. This results in de facto assortative mating when sexual forms are produced in late summer. Second, specialized aphids that are held on the alternate host will not feed in a 7.2-h trial, even in the face of starvation. Thus, a complex trait, behavioral acceptance of a plant as host, influences both reproductive isolation (through host-associated assortative mating) and ecological specialization (because of low nutritional uptake on the alternate host). This dual influence of feeding behavior on both assortative mating and resource specialization is central to the maintenance of these divergent races, and it may also have been involved in their origin.

Entities:  

Keywords:  ecological speciation; host races; insect‐plant interactions; local adaptation; sympatric speciation; trade‐offs

Year:  2000        PMID: 29592544     DOI: 10.1086/316991

Source DB:  PubMed          Journal:  Am Nat        ISSN: 0003-0147            Impact factor:   3.926


  16 in total

1.  Temporal habitat variability and the maintenance of sex in host populations of the pea aphid.

Authors:  Adrien Frantz; Manuel Plantegenest; Jean-Christophe Simon
Journal:  Proc Biol Sci       Date:  2006-11-22       Impact factor: 5.349

2.  Secondary Symbionts Affect Foraging Capacities of Plant-Specialized Genotypes of the Pea Aphid.

Authors:  Jean-Christophe Simon; Yannick Outreman; Corentin Sochard; Corentin Dupont
Journal:  Microb Ecol       Date:  2021-03-11       Impact factor: 4.552

3.  Complex evolution in Aphis gossypii group (Hemiptera: Aphididae), evidence of primary host shift and hybridization between sympatric species.

Authors:  Yerim Lee; Thomas Thieme; Hyojoong Kim
Journal:  PLoS One       Date:  2021-02-04       Impact factor: 3.240

4.  Cryptic virulence and avirulence alleles revealed by controlled sexual recombination in pea aphids.

Authors:  Sadia Kanvil; C Matilda Collins; Glen Powell; Colin G N Turnbull
Journal:  Genetics       Date:  2014-12-17       Impact factor: 4.562

5.  Intrinsic pre-zygotic reproductive isolation of distantly related pea aphid host races.

Authors:  Varvara Fazalova; Bruno Nevado; Ailsa McLean; H Charles J Godfray
Journal:  Biol Lett       Date:  2018-11-28       Impact factor: 3.703

6.  Vector-borne plant pathogens modify top-down and bottom-up effects on insect herbivores.

Authors:  Robert E Clark; David W Crowder
Journal:  Oecologia       Date:  2021-07-17       Impact factor: 3.225

7.  Partitioning the effects of spatial isolation, nest habitat, and individual diet in causing assortative mating within a population of threespine stickleback.

Authors:  L K Snowberg; D I Bolnick
Journal:  Evolution       Date:  2012-06-11       Impact factor: 3.694

8.  Antixenosis in Glycine max (L.) Merr against Acyrthosiphon pisum (Harris).

Authors:  Katarzyna Stec; Bożena Kordan; Iwona Sergiel; Magdalena Biesaga; Joanna Mroczek; Jan Bocianowski; Beata Gabryś
Journal:  Sci Rep       Date:  2021-07-27       Impact factor: 4.379

9.  DNA barcoding and the associated PhylAphidB@se website for the identification of European aphids (Insecta: Hemiptera: Aphididae).

Authors:  Armelle Coeur d'Acier; Astrid Cruaud; Emmanuelle Artige; Gwenaëlle Genson; Anne-Laure Clamens; Eric Pierre; Sylvie Hudaverdian; Jean-Christophe Simon; Emmanuelle Jousselin; Jean-Yves Rasplus
Journal:  PLoS One       Date:  2014-06-04       Impact factor: 3.240

10.  Aphid-encoded variability in susceptibility to a parasitoid.

Authors:  Adam J Martinez; Shannon G Ritter; Matthew R Doremus; Jacob A Russell; Kerry M Oliver
Journal:  BMC Evol Biol       Date:  2014-06-10       Impact factor: 3.260

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