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Delving into Delias Hübner (Lepidoptera: Pieridae): fine‐scale biogeography, phylogenetics and systematics of the world's largest butterfly genus

Identifieur interne : 000E50 ( Istex/Corpus ); précédent : 000E49; suivant : 000E51

Delving into Delias Hübner (Lepidoptera: Pieridae): fine‐scale biogeography, phylogenetics and systematics of the world's largest butterfly genus

Auteurs : Chris J. Müller ; Pável F. Matos-Maraví ; Luciano B. Beheregaray

Source :

RBID : ISTEX:BC8F9496CD81ADD9534C46A7F75768AF594A0097

Abstract

Our objective was to reconstruct a species‐level phylogeny of the genus Delias, to elucidate their finer‐scale biogeography and to test boundaries between closely related taxa.

Url:
DOI: 10.1111/jbi.12040

Links to Exploration step

ISTEX:BC8F9496CD81ADD9534C46A7F75768AF594A0097

Le document en format XML

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<note>Appendix S1 Exemplar taxa used in this study, with collection data and GenBank accession numbers.Appendix S2 Maximum parsimony and Bayesian trees for the combined cytochrome c oxidase subunit I (COI), elongation factor 1α (EF‐1α) and wingless dataset.Appendix S3 Delias systematics.</note>
<note>Oskar Öflunds</note>
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<forename type="first">Chris J.</forename>
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<affiliation>Correspondence: Chris J. Müller, Molecular Ecology Laboratory, Biological Sciences, Macquarie University, PO Box 3228, Dural, NSW 2158, Australia.E‐mail:</affiliation>
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<forename type="first">Pável F.</forename>
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<affiliation>Biology Center of the Czech Academy of Sciences and School of Biological Sciences, University of South Bohemia, 370 05, Ceske Budejovice, Czech Republic</affiliation>
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<forename type="first">Luciano B.</forename>
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<p>Our objective was to reconstruct a species‐level phylogeny of the genus Delias, to elucidate their finer‐scale biogeography and to test boundaries between closely related taxa.</p>
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<p>Sequence data from 131 taxa, representing all recognized species groups and more than half of the known species of Delias, were used in the analysis. Phylogenetic analyses based on molecular characters of the mitochondrial gene cytochrome c oxidase subunit I (COI) and nuclear genes wingless and elongation factor 1α (EF‐1α) were carried out using maximum parsimony and Bayesian inference. Biogeographical reconstructions were undertaken using the parsimony‐based method dispersal–vicariance analysis and the dispersal–extinction–cladogenesis model as implemented in rasp and Lagrange, respectively.</p>
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<p>The phylogenetic hypothesis resolved 14 distinct clades, here designated the nysa, isse, pasithoe, belladonna, ladas, geraldina, aroae, eichhorni, sagessa, aganippe, hyparete, belisama, albertisi and nigrina species groups. Delias blanca Felder and Delias chrysomelaena Snellen van Vollenhoven were transferred to the pasithoe and isse species groups, respectively. We demonstrate that the barcode region of COI is useful for the delineation of closely related, more recently diverged, Delias species. Species diversification in Delias, for the most part, is shown to pre‐date the Pleistocene, even in montane mainland New Guinea where numerous phenotypically similar sister species co‐occur.</p>
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<p>Sibling Delias species found in sympatry are largely restricted to those clades confined to mainland New Guinea, where most species occur in high‐elevation habitats. Conversely, clades with large geographical ranges are composed of essentially allopatric taxa. Although an Australian Plate origin is plausible for the genus, Delias is likely to have colonized islands peripheral to Australia during the early stages of its evolution (i.e. during the Miocene), as evidenced by the presence of older lineages in Wallacea and also in islands of the south‐western Pacific.</p>
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<doi origin="wiley" registered="yes">10.1111/(ISSN)1365-2699</doi>
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<title sort="JOURNAL OF BIOGEOGRAPHY" type="main">Journal of Biogeography</title>
<title type="short">J. Biogeogr.</title>
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<doi origin="wiley">10.1111/jbi.2013.40.issue-5</doi>
<copyright ownership="publisher">Copyright © 2013 Blackwell Publishing Ltd</copyright>
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<title type="articleCategory">Original Article</title>
<title type="tocHeading1">Animal histories</title>
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<copyright ownership="publisher">© 2012 Blackwell Publishing Ltd</copyright>
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<line>Correspondence: Chris J. Müller, Molecular Ecology Laboratory, Biological Sciences, Macquarie University, PO Box 3228, Dural, NSW 2158, Australia.</line>
<line>E‐mail:
<email>chrismuller999@gmail.com</email>
</line>
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<titleGroup>
<title type="main">Delving into
<i>Delias</i>
Hübner (Lepidoptera: Pieridae): fine‐scale biogeography, phylogenetics and systematics of the world's largest butterfly genus</title>
<title type="shortAuthors">C. J. Müller
<i>et al</i>
.</title>
</titleGroup>
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</personName>
</creator>
<creator affiliationRef="#jbi12040-aff-0002 #jbi12040-aff-0003" creatorRole="author" xml:id="jbi12040-cr-0002">
<personName>
<givenNames>Pável F.</givenNames>
<familyName>Matos‐Maraví</familyName>
</personName>
</creator>
<creator affiliationRef="#jbi12040-aff-0004" creatorRole="author" xml:id="jbi12040-cr-0003">
<personName>
<givenNames>Luciano B.</givenNames>
<familyName>Beheregaray</familyName>
</personName>
</creator>
<creator creatorRole="editor" xml:id="jbi12040-cr-0004">
<personName>
<givenNames>Malte</givenNames>
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<orgName>Macquarie University</orgName>
<address>
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<country>Australia</country>
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</affiliation>
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<city>Turku</city>
<country>Finland</country>
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<city>Ceske Budejovice</city>
<country>Czech Republic</country>
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</affiliation>
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<orgDiv>Molecular Ecology Laboratory, School of Biological Sciences</orgDiv>
<orgName>Flinders University</orgName>
<address>
<city>Adelaide</city>
<postCode>SA 5001</postCode>
<country>Australia</country>
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<keyword xml:id="jbi12040-kwd-0001">Butterflies</keyword>
<keyword xml:id="jbi12040-kwd-0002">
<fc>DEC</fc>
model</keyword>
<keyword xml:id="jbi12040-kwd-0003">historical biogeography</keyword>
<keyword xml:id="jbi12040-kwd-0004">Indo‐Australian region</keyword>
<keyword xml:id="jbi12040-kwd-0005">Miocene</keyword>
<keyword xml:id="jbi12040-kwd-0006">molecular phylogeny</keyword>
<keyword xml:id="jbi12040-kwd-0007">Müllerian mimicry</keyword>
<keyword xml:id="jbi12040-kwd-0008">plate tectonics</keyword>
<keyword xml:id="jbi12040-kwd-0009">Pliocene</keyword>
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<fundingAgency>Oskar Öflunds</fundingAgency>
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<fundingAgency>Turku University Foundations</fundingAgency>
</fundingInfo>
<fundingInfo>
<fundingAgency>Academy of Finland</fundingAgency>
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<fundingInfo>
<fundingAgency>Kone Foundation</fundingAgency>
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<b>Appendix S1</b>
Exemplar taxa used in this study, with collection data and GenBank accession numbers.</caption>
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<caption>
<b>Appendix S2</b>
Maximum parsimony and Bayesian trees for the combined cytochrome
<i>c</i>
oxidase subunit I (
<i>COI</i>
), elongation factor 1α (
<i>EF‐1</i>
α) and
<i>wingless</i>
dataset.</caption>
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<b>Appendix S3 </b>
<i>Delias</i>
systematics.</caption>
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<title type="main">Abstract</title>
<section xml:id="jbi12040-sec-0001">
<title type="main">Aim</title>
<p>Our objective was to reconstruct a species‐level phylogeny of the genus
<i>Delias</i>
, to elucidate their finer‐scale biogeography and to test boundaries between closely related taxa.</p>
</section>
<section xml:id="jbi12040-sec-0002">
<title type="main">Location</title>
<p>Indo‐Australian region, with a focus on Wallacea.</p>
</section>
<section xml:id="jbi12040-sec-0003">
<title type="main">Methods</title>
<p>Sequence data from 131 taxa, representing all recognized species groups and more than half of the known species of
<i>Delias</i>
, were used in the analysis. Phylogenetic analyses based on molecular characters of the mitochondrial gene cytochrome
<i>c</i>
oxidase subunit I (
<i>COI</i>
) and nuclear genes
<i>wingless</i>
and elongation factor 1α (
<i>EF‐1α</i>
) were carried out using maximum parsimony and Bayesian inference. Biogeographical reconstructions were undertaken using the parsimony‐based method dispersal–vicariance analysis and the dispersal–extinction–cladogenesis model as implemented in
<sc>rasp</sc>
and
<sc>Lagrange</sc>
, respectively.</p>
</section>
<section xml:id="jbi12040-sec-0004">
<title type="main">Results</title>
<p>The phylogenetic hypothesis resolved 14 distinct clades, here designated the
<i>nysa</i>
,
<i> isse</i>
,
<i> pasithoe</i>
,
<i> belladonna</i>
,
<i> ladas</i>
,
<i> geraldina</i>
,
<i> aroae</i>
,
<i> eichhorni</i>
,
<i> sagessa</i>
,
<i> aganippe</i>
,
<i> hyparete</i>
,
<i> belisama</i>
,
<i> albertisi</i>
and
<i>nigrina</i>
species groups.
<i>Delias blanca</i>
Felder and
<i>Delias chrysomelaena</i>
Snellen van Vollenhoven were transferred to the
<i>pasithoe</i>
and
<i>isse</i>
species groups, respectively. We demonstrate that the barcode region of
<i>
<fc>COI</fc>
</i>
is useful for the delineation of closely related, more recently diverged,
<i>Delias</i>
species. Species diversification in
<i>Delias</i>
, for the most part, is shown to pre‐date the Pleistocene, even in montane mainland New Guinea where numerous phenotypically similar sister species co‐occur.</p>
</section>
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<title type="main">Main conclusions</title>
<p>Sibling
<i>Delias</i>
species found in sympatry are largely restricted to those clades confined to mainland New Guinea, where most species occur in high‐elevation habitats. Conversely, clades with large geographical ranges are composed of essentially allopatric taxa. Although an Australian Plate origin is plausible for the genus,
<i>Delias</i>
is likely to have colonized islands peripheral to Australia during the early stages of its evolution (i.e. during the Miocene), as evidenced by the presence of older lineages in Wallacea and also in islands of the south‐western Pacific.</p>
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<title>Delving into Delias Hübner (Lepidoptera: Pieridae): fine‐scale biogeography, phylogenetics and systematics of the world's largest butterfly genus</title>
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<affiliation>Correspondence: Chris J. Müller, Molecular Ecology Laboratory, Biological Sciences, Macquarie University, PO Box 3228, Dural, NSW 2158, Australia.E‐mail:</affiliation>
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<affiliation>Biology Center of the Czech Academy of Sciences and School of Biological Sciences, University of South Bohemia, 370 05, Ceske Budejovice, Czech Republic</affiliation>
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<abstract>Our objective was to reconstruct a species‐level phylogeny of the genus Delias, to elucidate their finer‐scale biogeography and to test boundaries between closely related taxa.</abstract>
<abstract>Indo‐Australian region, with a focus on Wallacea.</abstract>
<abstract>Sequence data from 131 taxa, representing all recognized species groups and more than half of the known species of Delias, were used in the analysis. Phylogenetic analyses based on molecular characters of the mitochondrial gene cytochrome c oxidase subunit I (COI) and nuclear genes wingless and elongation factor 1α (EF‐1α) were carried out using maximum parsimony and Bayesian inference. Biogeographical reconstructions were undertaken using the parsimony‐based method dispersal–vicariance analysis and the dispersal–extinction–cladogenesis model as implemented in rasp and Lagrange, respectively.</abstract>
<abstract>The phylogenetic hypothesis resolved 14 distinct clades, here designated the nysa, isse, pasithoe, belladonna, ladas, geraldina, aroae, eichhorni, sagessa, aganippe, hyparete, belisama, albertisi and nigrina species groups. Delias blanca Felder and Delias chrysomelaena Snellen van Vollenhoven were transferred to the pasithoe and isse species groups, respectively. We demonstrate that the barcode region of COI is useful for the delineation of closely related, more recently diverged, Delias species. Species diversification in Delias, for the most part, is shown to pre‐date the Pleistocene, even in montane mainland New Guinea where numerous phenotypically similar sister species co‐occur.</abstract>
<abstract>Sibling Delias species found in sympatry are largely restricted to those clades confined to mainland New Guinea, where most species occur in high‐elevation habitats. Conversely, clades with large geographical ranges are composed of essentially allopatric taxa. Although an Australian Plate origin is plausible for the genus, Delias is likely to have colonized islands peripheral to Australia during the early stages of its evolution (i.e. during the Miocene), as evidenced by the presence of older lineages in Wallacea and also in islands of the south‐western Pacific.</abstract>
<note type="additional physical form">Appendix S1 Exemplar taxa used in this study, with collection data and GenBank accession numbers.Appendix S2 Maximum parsimony and Bayesian trees for the combined cytochrome c oxidase subunit I (COI), elongation factor 1α (EF‐1α) and wingless dataset.Appendix S3 Delias systematics.</note>
<note type="funding">Oskar Öflunds</note>
<note type="funding">Turku University Foundations</note>
<note type="funding">Academy of Finland</note>
<note type="funding">Kone Foundation</note>
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<topic>Butterflies</topic>
<topic>DEC model</topic>
<topic>historical biogeography</topic>
<topic>Indo‐Australian region</topic>
<topic>Miocene</topic>
<topic>molecular phylogeny</topic>
<topic>Müllerian mimicry</topic>
<topic>plate tectonics</topic>
<topic>Pliocene</topic>
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