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      Congruence and Diversity of Butterfly-Host Plant Associations at Higher Taxonomic Levels

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          Summary

          A macro-evolution analysis of biotic interactions between butterflies and their hostplants. For this analysis we compiled known larval hostplant records from scientific literature, field observations and existing databases.

          The relationship between butterflies and their hostplants is one of the most illustrative examples of the evolution of ecological interactions between large evolutionary lineages.

          Abstract

          We aggregated data on butterfly-host plant associations from existing sources in order to address the following questions: (1) is there a general correlation between host diversity and butterfly species richness?, (2) has the evolution of host plant use followed consistent patterns across butterfly lineages?, (3) what is the common ancestral host plant for all butterfly lineages? The compilation included 44,148 records from 5,152 butterfly species (28.6% of worldwide species of Papilionoidea) and 1,193 genera (66.3%). The overwhelming majority of butterflies use angiosperms as host plants. Fabales is used by most species (1,007 spp.) from all seven butterfly families and most subfamilies, Poales is the second most frequently used order, but is mostly restricted to two species-rich subfamilies: Hesperiinae (56.5% of all Hesperiidae), and Satyrinae (42.6% of all Nymphalidae). We found a significant and strong correlation between host plant diversity and butterfly species richness. A global test for congruence (Parafit test) was sensitive to uncertainty in the butterfly cladogram, and suggests a mixed system with congruent associations between Papilionidae and magnoliids, Hesperiidae and monocots, and the remaining subfamilies with the eudicots (fabids and malvids), but also numerous random associations. The congruent associations are also recovered as the most probable ancestral states in each node using maximum likelihood methods. The shift from basal groups to eudicots appears to be more likely than the other way around, with the only exception being a Satyrine-clade within the Nymphalidae that feed on monocots. Our analysis contributes to the visualization of the complex pattern of interactions at superfamily level and provides a context to discuss the timing of changes in host plant utilization that might have promoted diversification in some butterfly lineages.

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          Most cited references14

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          A statistical test for host-parasite coevolution.

          A new method, ParaFit, has been developed to test the significance of a global hypothesis of coevolution between parasites and their hosts. Individual host-parasite association links can also be tested. The test statistics are functions of the host and parasite phylogenetic trees and of the set of host-parasite association links. Numerical simulations are used to show that the method has correct rate of type I error and good power except under extreme error conditions. An application to real data (pocket gophers and chewing lice) is presented.
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            The ecology and evolution of ant association in the Lycaenidae (Lepidoptera).

            The estimated 6000 species of Lycaenidae account for about one third of all Papilionoidea. The majority of lycaenids have associations with ants that can be facultative or obligate and range from mutualism to parasitism. Lycaenid larvae and pupae employ complex chemical and acoustical signals to manipulate ants. Cost/benefit analyses have demonstrated multiple trade-offs involved in myrmecophily. Both demographic and phylogenetic evidence indicate that ant association has shaped the evolution of obligately associated groups. Parasitism typically arises from mutualism with ants, and entomophagous species are disproportionately common in the Lycaenidae compared with other Lepidoptera. Obligate associations are more common in the Southern Hemisphere, in part because highly ant-associated lineages make up a larger proportion of the fauna in these regions. Further research on phylogeny and natural history, particularly of the Neotropical fauna, will be necessary to understand the role ant association has played in the evolution of the Lycaenidae.
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              What causes latitudinal gradients in species diversity? Evolutionary processes and ecological constraints on swallowtail biodiversity.

              The latitudinal diversity gradient (LDG) is one of the most striking ecological patterns on our planet. Determining the evolutionary causes of this pattern remains a challenging task. To address this issue, previous LDG studies have usually relied on correlations between environmental variables and species richness, only considering evolutionary processes indirectly. Instead, we use a phylogenetically integrated approach to investigate the ecological and evolutionary processes responsible for the global LDG observed in swallowtail butterflies (Papilionidae). We find evidence for the 'diversification rate hypothesis' with different diversification rates between two similarly aged tropical and temperate clades. We conclude that the LDG is caused by (1) climatically driven changes in both clades based on evidence of responses to cooling and warming events, and (2) distinct biogeographical histories constrained by tropical niche conservatism and niche evolution. This multidisciplinary approach provides new findings that allow better understanding of the factors that shape LDGs. © 2012 Blackwell Publishing Ltd/CNRS.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2013
                23 May 2013
                : 8
                : 5
                : e63570
                Affiliations
                [1 ]Kirstenbosch Research Centre, South African National Biodiversity Institute, Cape Town, Western Cape, Republic of South Africa
                [2 ]Botany Department, University of Cape Town, Cape Town, Western Cape, Republic of South Africa
                [3 ]Centro de Estudios Botánicos y Agroforestales, Instituto Venezolano de Investigaciones Científicas, Maracaibo, Estado Zulia, Venezuela
                [4 ]Centro de Ecología, Instituto Venezolano de Investigaciones Científicas, Caracas, Distrito Capital, Venezuela
                University Copenhagen, Denmark
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: JRFP ASM. Performed the experiments: JRFP ASM. Analyzed the data: JRFP. Wrote the paper: JRFP ASM ALV JD.

                Article
                PONE-D-13-04262
                10.1371/journal.pone.0063570
                3662771
                23717448
                f1fdd0fb-f57a-4b8b-abdf-9386e1d29c6f
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 22 January 2013
                : 4 April 2013
                Page count
                Pages: 15
                Funding
                This work was supported by Instituto Venezolano de Investigaciones Científicas (IVIC), and by a postdoctoral fellowship “Threatened species program” from South African National Biodiversity Institute (SANBI) and University of Cape Town (UCT) to ASM and JRFP. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Ecology
                Community Ecology
                Food Web Structure
                Species Interactions
                Trophic Interactions
                Biodiversity
                Evolutionary Ecology
                Evolutionary Biology
                Evolutionary Processes
                Coevolution
                Speciation
                Forms of Evolution
                Coevolution
                Macroevolution
                Evolutionary Ecology

                The datasets generated during and/or analysed during the current study are available in the repository: https://doi.org/10.6084/m9.figshare.1168861.v1
                Evolutionary Biology,Ecology,Life sciences
                macroevolution
                The datasets generated during and/or analysed during the current study are available in the repository: https://doi.org/10.6084/m9.figshare.1168861.v1
                Evolutionary Biology, Ecology, Life sciences
                macroevolution

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