Towards a global DNA barcode reference library for quarantine identifications of lepidopteran stemborers, with an emphasis on sugarcane pests

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作者
Timothy R. C. Lee
Stacey J. Anderson
Lucy T. T. Tran-Nguyen
Nader Sallam
Bruno P. Le Ru
Desmond Conlong
Kevin Powell
Andrew Ward
Andrew Mitchell
机构
[1] Australian Museum Research Institute,Department of Entomology
[2] Department of Agriculture and Water Resources,Biosecurity Operations, NAQS
[3] Northern Territory Department of Primary Industry and Resources,Department of Agriculture and Water Resources
[4] GPO Box 3000,Department of Conservation Ecology and Entomology, Faculty of AgriSciences
[5] 114 Catalina Crescent,undefined
[6] Airport Business Park,undefined
[7] Cairns Airport,undefined
[8] African Insect Science for Food and Health (ICIPE),undefined
[9] IRD/CNRS,undefined
[10] UMR IRD 247 EGCE,undefined
[11] Laboratoire Evolution Génomes Comportement et Ecologie,undefined
[12] Avenue de la terrasse,undefined
[13] BP1,undefined
[14] 91198,undefined
[15] Gif-sur-Yvette,undefined
[16] France and Université Paris-Sud 11,undefined
[17] University of Stellenbosch,undefined
[18] Private Bag X1,undefined
[19] South African Sugarcane Research Institute,undefined
[20] Sugar Research Australia,undefined
[21] Sugar Research Australia,undefined
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摘要
Lepidopteran stemborers are among the most damaging agricultural pests worldwide, able to reduce crop yields by up to 40%. Sugarcane is the world’s most prolific crop, and several stemborer species from the families Noctuidae, Tortricidae, Crambidae and Pyralidae attack sugarcane. Australia is currently free of the most damaging stemborers, but biosecurity efforts are hampered by the difficulty in morphologically distinguishing stemborer species. Here we assess the utility of DNA barcoding in identifying stemborer pest species. We review the current state of the COI barcode sequence library for sugarcane stemborers, assembling a dataset of 1297 sequences from 64 species. Sequences were from specimens collected and identified in this study, downloaded from BOLD or requested from other authors. We performed species delimitation analyses to assess species diversity and the effectiveness of barcoding in this group. Seven species exhibited <0.03 K2P interspecific diversity, indicating that diagnostic barcoding will work well in most of the studied taxa. We identified 24 instances of identification errors in the online database, which has hampered unambiguous stemborer identification using barcodes. Instances of very high within-species diversity indicate that nuclear markers (e.g. 18S, 28S) and additional morphological data (genitalia dissection of all lineages) are needed to confirm species boundaries.
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