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    A Novel, Enigmatic Basal Leafflower Moth Lineage Pollinating a Derived Leafflower Host Illustrates the Dynamics of Host Shifts, Partner Replacement, and Apparent Coadaptation in Intimate Mutualisms

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    Author
    Luo, Shi-Xiao
    Yao, Gang
    Wang, Ziwei
    Zhang, Dianxiang
    Hembry, David H.
    Affiliation
    Univ Arizona, Dept Ecol & Evolutionary Biol
    Issue Date
    2017-04
    Keywords
    Epicephala
    Glochidion
    host shift
    intimate mutualism
    specialized pollination
    coadaptation
    
    Metadata
    Show full item record
    Publisher
    UNIV CHICAGO PRESS
    Citation
    A Novel, Enigmatic Basal Leafflower Moth Lineage Pollinating a Derived Leafflower Host Illustrates the Dynamics of Host Shifts, Partner Replacement, and Apparent Coadaptation in Intimate Mutualisms 2017, 189 (4):422 The American Naturalist
    Journal
    The American Naturalist
    Rights
    © 2017 by The University of Chicago. All rights reserved.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Leafflower plant/leafflower moth brood pollination mutualisms are widespread in the Paleotropics. Leafflower moths pollinate leafflower plants, but their larvae consume a subset of the hosts' seeds. These interactions are highly phylogenetically constrained: six clades of leafflower plants are each associated with a unique clade of leafflower moths (Epicephala). Here, we report a previously unrecognized basal seventh pollinating Epicephala lineageassociated with the highly derived leafflower clade Glochidionin Asia. Epicephala lanceolaria is a pollinator and seed predator of Glochidion lanceolarium. Phylogenetic inference indicates that the ancestor of E. lanceolaria most likely shifted onto the ancestor of G. lanceolarium and displaced the ancestral allospecific Epicephala pollinator in at least some host populations. The unusual and apparently coadapted aspects of the G. lanceolarium/E. lanceolaria reproductive cycles suggest that plant-pollinator coevolution may have played a role in this displacement and provide insights into the dynamics of host shifts and trait coevolution in this specialized mutualism.
    Note
    12 month embargo; Published Online: Jan 12, 2017
    ISSN
    0003-0147
    1537-5323
    PubMed ID
    28350503
    DOI
    10.1086/690623
    Version
    Final published version
    Sponsors
    National Science Foundation of China [31370268, 30700044]; National Science Foundation (NSF) [ACI-1053575]; NSF [OISE-1159509]; National Institutes of Health Postdoctoral Excellence in Research and Teaching program at the University of Arizona
    Additional Links
    http://www.journals.uchicago.edu/doi/10.1086/690623
    ae974a485f413a2113503eed53cd6c53
    10.1086/690623
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    UA Faculty Publications

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