Publications by authors named "M L Starkie"

Article Synopsis
  • Insects collected in dry traps can degrade quickly in warm, humid conditions, which affects identification efforts for biosecurity surveillance, particularly for tephritid fruit flies.
  • A controlled study showed that higher temperature and humidity levels significantly increased DNA degradation, especially at 35 °C and 90% humidity, while fluctuating temperatures had little effect.
  • The research suggests that improving trap clearance times and design could enhance the reliability of DNA for surveillance activities, with further investigation needed on other environmental factors influencing DNA quality.
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Bactrocera tryoni and Bactrocera neohumeralis are morphologically similar sibling pest fruit fly species that possess different biological attributes, geographic distributions, and host ranges. The need to differentiate between the two species is critical for accurate pest status assessment, management, biosecurity, and maintenance of reference colonies. While morphologically similar, adults may be separated based on subtle characters; however, some characters exhibit intraspecific variability, creating overlap between the two species.

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The potential for population genomics to elucidate invasion pathways of a species is limited by taxonomic identification issues. The Oriental fruit fly pest, Bactrocera dorsalis (Hendel) belongs to a complex in which several sympatric species are attracted to the same lure used in trapping and are morphologically cryptic and/or reported to hybridize. In this study, we evaluated the taxonomic ambiguity between B.

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Insect identification and preservation of voucher specimens is integral to pest diagnostic and surveillance activities; yet bulk-trapped insects are a diagnostic challenge due to high catch numbers and the susceptibility of samples to environmental damage. Many insect trap catches rely on examination of morphological characters for species identifications, which is a time consuming and highly skilled task, hence there is a need for more efficient molecular approaches. Many bulk DNA extraction methods require destructive sampling of specimens, resulting in damaged, or fully destroyed, voucher specimens.

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