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Article << Previous     |     Next >>   Contents Vol 26(6)

Difficulties barcoding in the dark: the case of crustacean stygofauna from eastern Australia

Maria G. Asmyhr A D and Steven J. B. Cooper B C

A Department of Biological Sciences, Macquarie University, Sydney, NSW 2109, Australia.
B Evolutionary Biology Unit, South Australian Museum, North Terrace, Adelaide, SA 5000, Australia.
C Australian Centre for Evolutionary Biology and Biodiversity, The University of Adelaide, SA 5005, Australia.
D Corresponding author. Email: maria.asmyhr@mq.edu.au

Invertebrate Systematics 26(6) 583-591 http://dx.doi.org/10.1071/IS12032
Submitted: 26 April 2012  Accepted: 19 September 2012   Published: 19 December 2012


 
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Abstract

The eastern Australian aquifers remain mostly unexplored; however, recent surveys suggest that there could be substantial levels of subterranean biodiversity hidden in these aquifers. Groundwater fauna (stygofauna) is often characterised by short-range endemism. Furthermore, high levels of cryptic species, and lack of formal taxonomic descriptions and taxonomic expertise for many of the groups demand innovative approaches for assessing subterranean biodiversity. Here we evaluate the potential of using DNA barcoding as a rapid biodiversity assessment tool for the subterranean groundwater fauna of New South Wales, Australia. We experienced low amplification success using universal and more taxon-specific primers for PCR amplification of the barcoding gene (COI) in a range of crustacean stygofauna. Sequence comparisons of the most commonly used COI universal primers in selected crustacean taxa revealed high levels of variability. Our results suggest that successful amplification of the COI region from crustacean stygofauna is not straightforward using the standard ‘universal’ primers. We propose that the development of a multiprimer (taxon specific) and multigene approach for DNA barcode analyses, using next-generation sequencing methodologies, will help to overcome many of the technical problems reported here and provide a basis for using DNA barcoding for rapid biodiversity assessments of subterranean aquatic ecosystems.



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