DNA barcoding unravels contrasting evolutionary history of two widespread Asian tiger moth species during the Late Pleistocene.
Vitaly M SpitsynAlexander V KondakovNikita I BolotovNhi Thi PhamMikhail Y GofarovIvan N BolotovPublished in: PloS one (2018)
Populations of widespread pest insects in tropical areas are characterized by a complex evolutionary history, with overlapping natural and human-mediated dispersal events, sudden expansions, and bottlenecks. Here, we provide biogeographic reconstructions for two widespread pest species in the tiger moth genus Creatonotos (Lepidoptera: Erebidae: Arctiinae) based on the mitochondrial cytochrome c oxidase subunit I (COI) gene. The Asian Creatonotos transiens reveals shallow genetic divergence between distant populations that does not support its current intraspecific systematics with several local subspecies. In contrast, the more widespread Creatonotos gangis comprises at least three divergent subclades corresponding to certain geographic areas, i.e. Australia, Arabia + South Asia and Southeast Asia. With respect to our approximate Bayesian computation (ABC) model, the expansion of Creatonotos gangis into Australia is placed in the Late Pleistocene (~65-63 ka). This dating coincide with an approximate time of the earliest human migration into the continent (~65-54 ka) and the period of intervisibility between Timor and Australia (~65-62 ka). Our findings highlight that the drying Sunda and Sahul shelf areas likely support successful migrations of Asian taxa into Australia during the Pleistocene. The phylogeographic patterns discovered in this study can be used to improve the effectiveness of integrated pest control programs that is a task of substantial practical importance to a broad range of agricultural stakeholders.
Keyphrases
- genome wide
- endothelial cells
- genetic diversity
- induced pluripotent stem cells
- randomized controlled trial
- climate change
- magnetic resonance
- pluripotent stem cells
- public health
- copy number
- risk assessment
- healthcare
- single molecule
- circulating tumor
- cell free
- nucleic acid
- circulating tumor cells
- protein kinase
- affordable care act