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    Multiple incursions and putative species revealed using a mitochondrial and nuclear phylogenetic approach to the Trogoderma variabile (Coleoptera: Dermestidae) trapping program in Australia

    165542_165542.pdf (165.3Kb)
    Access Status
    Open access
    Authors
    Castalanelli, Mark
    Mikac, K.
    Baker, A.
    Munyard, Kylie
    Grimm, M.
    Groth, David
    Date
    2011
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Castalanelli, M.A. and Mikac, K.M. and Baker, A.M. and Munyard, K. and Grimm, M. and Groth, D.M. 2011. Multiple incursions and putative species revealed using a mitochondrial and nuclear phylogenetic approach to the Trogoderma variabile (Coleoptera: Dermestidae) trapping program in Australia. Bulletin of Entomological Research. 101: pp. 333-343.
    Source Title
    Bulletin of Entomological Research
    DOI
    10.1017/S0007485310000544
    ISSN
    00074853
    School
    School of Biomedical Sciences
    Remarks

    Copyright © 2011 Cambridge University Press

    URI
    http://hdl.handle.net/20.500.11937/31587
    Collection
    • Curtin Research Publications
    Abstract

    The Warehouse beetle, Trogoderma variabile (Coleoptera: Dermestidae), is an internationally significant invasive pest of packed goods and stored grain. When it was first documented in Australia at Griffith, New South Wales, in 1977, an eradication campaign was initiated. After several years and considerable effort, the eradication campaign was abandoned. To monitor the presence and spread of T. variabile, surveys were carried out by government agencies in 1992 and 2002. When survey data was compared, it was concluded that the distribution of morphologically identified T. variabile had doubled in most Australian states. Here, we used samples from the 2002 survey to conduct a phylogenetic study using partial sequences of mitochondrial genes Cytochrome oxidase I and Cytochrome B, and the nuclear gene 18S, to examine the distribution and dispersal of T. variabile and detect the presence of misidentified species. Based on our molecular results, we show that only 47% of the samples analysed were T. variabile, and the remaining were a mixture of six putative species. In addition, T. variabile was found in only 78% of the trapping sites. We discuss the importance of correct diagnosis in relation to the eradication campaign.

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