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.2015 Dec 14;10(12):e0144966.
doi: 10.1371/journal.pone.0144966. eCollection 2015.

Coalescent Modelling Suggests Recent Secondary-Contact of Cryptic Penguin Species

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Coalescent Modelling Suggests Recent Secondary-Contact of Cryptic Penguin Species

Stefanie Grosser et al. PLoS One..

Abstract

Molecular genetic analyses present powerful tools for elucidating demographic and biogeographic histories of taxa. Here we present genetic evidence showing a dynamic history for two cryptic lineages within Eudyptula, the world's smallest penguin. Specifically, we use a suite of genetic markers to reveal that two congeneric taxa ('Australia' and 'New Zealand') co-occur in southern New Zealand, with only low levels of hybridization. Coalescent modelling suggests that the Australian little penguin only recently expanded into southern New Zealand. Analyses conducted under time-dependent molecular evolutionary rates lend support to the hypothesis of recent anthropogenic turnover, consistent with shifts detected in several other New Zealand coastal vertebrate taxa. This apparent turnover event highlights the dynamic nature of the region's coastal ecosystem.

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Conflict of interest statement

Competing Interests:The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Map of distribution ofEudyptula penguins.
Blue and red colours indicate previously-inferred ranges of New Zealand and Australian mitochondrial lineages [18,19], respectively. Lineage distributions in grey dashed areas are unknown. White circles mark sampling localities for the current study. Black lines indicate proximate samples pooled asa priori regional groupings to increase population sample size.
Fig 2
Fig 2. Genetic clustering ofE.minor samples based on STRUCTURE analysis forK = 2.
Horizontal and vertical bars represent proportional membership of individuals to genetic clusters. Individuals between black lines represent distinct sampling localities as indicated on the map.
Fig 3
Fig 3. Median-joining network ofEudyptula mitochondrial control region haplotypes.
Circle size is proportional to haplotype frequency. Colours represent different sampling locations as indicated on the map. Edges between haplotypes represent single mutational steps. Unobserved haplotypes are indicated by small black circles. The red and blue boxes indicate AUS and NZ lineages, respectively.
Fig 4
Fig 4. Median-joining network ofEudyptula β-fibrinogen intron 7 alleles.
Circle size is proportional to allele frequency. Colours represent sampling locations from Australia and Otago (red) and all other NZ locations (blue). Edges between alleles represent single mutational steps. The red and blue boxes contain alleles associated with AUS and NZ lineages ofE.minor, respectively.
Fig 5
Fig 5. Individual assignment to genetic clusters and hybrid ancestry as determined by STRUCTURE assignment test (bottom plot) and NEWHYBRIDS (top plot).
Sampling locations are separated by black vertical lines. Individuals are represented by vertical bars where the colour represents the posterior probability of ancestry of being NZ lineage (blue), AUS lineage (red), a first generation hybrid (F1; purple), a second generation hybrid (F2; pink), a backcross between a F1 and NZ lineage individual (yellow), a backcross between a F1 and AUS lineage individual (orange) or a F2/backcross with either lineage (white; for STRUCTURE plot only). The grey horizontal line indicates 50% posterior probability threshold.
Fig 6
Fig 6. Posterior distributions from analysis under the ‘Isolation with Migration’ model for Otago and Phillip Island populations.
Results are presented for analyses with and without post-divergence gene flow (migration). All parameters are scaled by mutation rate. Note that the migration posteriors are described in coalescent terms (movement backwards through time).
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References

    1. Avise JC. Molecular markers, natural history, and evolution 2nd Edition Sunderland, MA: Sinauer Associates; 2004.
    1. Beaumont MA. Approximate Bayesian Computation in Evolution and Ecology. Annu Rev Ecol Evol S. 2010;41(1): 379–406. 10.1146/annurev-ecolsys-102209-144621 - DOI
    1. Barnes I, Matheus P, Shapiro B, Jensen D, A. C. Dynamics of Pleistocene population extinctions in Beringian brown bears. Science. 2002;295: 2267–2270. - PubMed
    1. Hofreiter M, Muenzel S, Conard NJ, Pollack J, Slatkin M, Weiss G, et al. Sudden replacement of cave bear mitochondrial DNA in the late Pleistocene. Current Biology. 2007;17: R122–R3. - PubMed
    1. Boessenkool S, Austin JJ, Worthy TH, Scofield P, Cooper A, Seddon PJ, et al. Relict or colonizer? Extinction and range expansion of penguins in southern New Zealand. Proc R Soc B. 2009;276(1658): 815–821. 10.1098/rspb.2008.1246 - DOI - PMC - PubMed

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