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Allozyme and mitochondrial DNA variability within the New Zealand damselfly genera Xanthocnemis,Austrolestes, and Ischnura (Odonata)
Authors:Liam Nolan  Ian D. Hogg  Darin L. Sutherland  Mark I. Stevens  Kareen E. Schnabel
Affiliation:1. Centre for Biodiversity and Ecology Research, Department of Biological Sciences , University of Waikato , Private Bag 3105, Hamilton, 3240, New Zealand;2. Cirencester College , Fosse Way Campus, Stroud Road, Cirencester, S Glos, United Kingdom;3. Centre for Biodiversity and Ecology Research, Department of Biological Sciences , University of Waikato , Private Bag 3105, Hamilton, 3240, New Zealand E-mail: hogg@waikato.ac.nz;4. West Coast Conservancy, Department of Conservation , Private Bag 701, Hokitika, 7842, New Zealand;5. Allan Wilson Centre for Molecular Ecology &6. Evolution , Massey University , Private Bag 11222, Palmerston North, 4442, New Zealand;7. School of Biological Sciences , Monash University , Clayton, Victoria, 3800, Australia;8. Marine Biodiversity and Biose‐curity National Institute of Water and Atmospheric Research (NIWA) Ltd , Private Bag 14901, Kilbirnie, Wellington, 6241, New Zealand
Abstract:Abstract

We collected larval damselflies from 17 sites in the North, South and Chatham Islands, and tested the hypotheses that: (1) genetic markers (e.g., allozymes, mtDNA) would successfully discriminate taxa; and (2) the dispersal capabilities of adult damselflies would limit differentiation among locations. Four species from three genera were identified based on available taxonomic keys. Using 11 allozyme loci and the mitochondrial cytochrome c‐oxidase subunit I (COI) gene, we confirmed that all taxa were clearly discernible. We found evidence for low to moderate differentiation among locations based on allozyme (meani F ST = 0.09) and sequence (COI) divergence (<0.034). No obvious patterns with respect to geographic location were detected, although slight differences were found between New Zealand's main islands (North Island, South Island) and the Chatham Islands for A. colensonis (sequence divergence 0.030–0.034). We also found limited intraspecific genetic variability based on allozyme data (Hexp < 0.06 in all cases). We conclude that levels of gene flow/dispersal on the main islands may have been sufficient to maintain the observed homogeneous population structure, and that genetic techniques, particularly the COI gene locus, will be a useful aid in future identifications.
Keywords:allozymes  COI  dispersal  DNA barcoding  gene flow  population genetics  Zy‐goptera
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