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Native New Zealand forget-me-nots (Myosotis, Boraginaceae) comprise a Pleistocene species radiation with very low genetic divergence

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Abstract

Reconstruction of molecular phylogenies is an important step towards understanding the evolutionary history of island plant radiations. The New Zealand forget-me-nots (Myosotis, Boraginaceae) comprise a lineage of over 40 closely related but morphologically and ecologically diverse species whose evolutionary history and taxonomy are unclear. Myosotis is a high priority for systematic research in New Zealand because a high proportion of these species are threatened, and many have restricted geographic ranges and occupy very specific habitats. Here, we investigated the relationships and age of Southern Hemisphere forget-me-nots by performing phylogenetic, molecular dating, and other analyses of DNA sequence datasets from representatives of nearly all described species. To this end, we used both chloroplast (atpI–atpH + rps16–trnQ) and nuclear ribosomal (ITS + ETS) DNA sequences, as well as amplified fragment length polymorphisms (AFLPs). Our analyses showed that genus Myosotis likely arose in the Northern Hemisphere during the Miocene with the ancestor of the Southern Hemisphere lineage arising in the Pleistocene and radiating shortly thereafter. The Southern Hemisphere Myosotis species have very low levels of genetic divergence and their relationships are largely unresolved, likely due to a combination of recent radiation, hybridization, and incomplete lineage sorting. Our results are compared to those of similar studies on other New Zealand species radiations, and implications for ongoing and future Myosotis taxonomic and evolutionary research are discussed.

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References

  • Albach DC, Meudt HM (2010) Phylogeny of Veronica in the Southern and Northern Hemispheres based on plastid, nuclear ribosomal and nuclear low-copy DNA. Molec Phylogenet Evol 54:457–471

    Article  CAS  PubMed  Google Scholar 

  • Bacon CD, Allan GJ, Zimmer EA, Wagner WL (2011) Genome scans reveal high levels of gene flow in Hawaiian Pittosporum. Taxon 60:733–741

    Google Scholar 

  • Baldwin BG, Markos S (1998) Phylogenetic utility of the external transcribed spacer (ETS) of 18S-26S rDNA: congruence of ETS and ITS trees of Calycadenia (Compositae). Molec Phylogenet Evol 10:449–463

    Article  CAS  PubMed  Google Scholar 

  • Beuzenberg EJ, Hair JB (1983) Contributions to a chromosome atlas of the New Zealand flora—25 miscellaneous species. New Zealand J Bot 21:13–20

    Google Scholar 

  • Bouckaert R, Heled J, Kühnert D, Vaughan T, Wu CH, Xie D, Suchard MA, Rambaut A, Drummond AJ (2014) BEAST 2: a software platform for Bayesian evolutionary analysis. PLoS Comput Biol 10:e1003537

    Article  PubMed Central  PubMed  Google Scholar 

  • Brandon AM (2001) Breeding systems and rarity in New Zealand Myosotis. Dissertation, Massey University, Palmerston North, New Zealand

  • Breitwieser I, Brownsey PJ, Garnock-Jones PJ, Perrie LR, Wilton A (2012) Phylum Tracheophyta, vascular plants. In: Gordon D (ed) The New Zealand inventory of biodiversity: a species 2000 symposium review. University of Canterbury Press, Christchurch, pp 411–459

    Google Scholar 

  • Cohen J, Davis J (2009) Nomenclatural changes in Lithospermum (Boraginaceae) and related taxa following a reassessment of phylogenetic relationships. Brittonia 61:101–111

    Article  Google Scholar 

  • Cohen J (2010) Continuous characters in phylogenetic analyses: patterns of corolla tube length evolution in Lithospermum L. (Boraginaceae). Biol J Linn Soc 107:442–457

    Article  Google Scholar 

  • Darriba D, Taboada GL, Doallo R, Posada D (2012) jModelTest 2: more models, new heuristics and parallel computing. Nature Meth 9:772

    Article  CAS  Google Scholar 

  • de Candolle AP (1846) Prodromus systematis naturalis regni vegetabilis. Treuttel et Wurtz, Paris, France

    Google Scholar 

  • de Lange PJ, Murray BG (2002) Contributions to a chromosome atlas of the New Zealand flora—37 miscellaneous families. New Zealand J Bot 40:1–23

    Article  Google Scholar 

  • de Lange PJ, Rolfe J (2010) New Zealand Indigenous Vascular Plant Checklist. New Zealand Plant Conservation Network, Wellington, New Zealand

    Google Scholar 

  • de Lange PJ, Norton DA, Courtney SP, Heenan PB, Barkla JW, Cameron EK, Hitchmough R, Townsend AJ (2009) Threatened and uncommon plants of New Zealand (2008 revision). New Zealand J Bot 47:61–96

    Article  Google Scholar 

  • de Lange PJ, Rolfe JR, Champion PD, Courtney SP, Heenan PB, Barkla JW, Cameron EW, Norton DA, Hitchmough RA (2013) Conservation status of New Zealand indigenous vascular plants, 2012 New Zealand threat classification series 3. Department of Conservation, Wellington, New Zealand

    Google Scholar 

  • Doyle JF, Dickson EE (1987) Preservation of plant samples for DNA restriction endonuclease analyses. Taxon 36:715–722

    Article  Google Scholar 

  • Druce AP (1993) Indigenous vascular plants of New Zealand, 9th revision. Landcare Research, Lower Hutt

    Google Scholar 

  • Drummond AJ, Ho SYW, Phillips MJ, Rambaut A (2006) Relaxed phylogenetics and dating with confidence. PLoS Biol 4:699–710

    Article  CAS  Google Scholar 

  • Drummond AJ, Ashton B, Cheung M, Heled J, Kearse M, Moir R, Stones-Havas S, Thierer T, Wilson A (2007) Geneious v 5.3.6 < http://www.geneiouscom/>

  • Ferrero V, Arroyo J, Vargas P, Thompson JD, Navarro L (2009) Evolutionary transitions of style polymorphisms in Lithodora (Boraginaceae). Perspect Pl Ecol Evol Syst 11:111–125

    Article  Google Scholar 

  • Fisher FJF (1965) The Alpine Ranunculi of New Zealand. New Zealand Department of Scientific and Industrial Research Bulletin 165:1–192

  • Ford KA, Ward JM, Smissen RD, Wagstaff SJ, Breitwieser I (2007) Phylogeny and biogeography of Craspedia (Asteraceae: Gnaphalieae) based on ITS, ETS and psbA-trnH sequence data. Taxon 56:783–794

    Article  Google Scholar 

  • Gabel ML (1987) Fossil Lithospermum (Boraginaceae) from the Tertiary of South Dakota. Amer J Bot 74:1690–1693

    Article  Google Scholar 

  • Gernhard T (2008a) The conditioned reconstructed process. J Theor Biol 253:769–778

    Article  PubMed  Google Scholar 

  • Gernhard T (2008b) New analytic results for speciation times in neutral models. Bull Math Biol 70:1082–1097

    Article  PubMed  Google Scholar 

  • Given DR (1981) Rare and endangered plants of New Zealand. Christchurch, AH and A W Reed Ltd

    Google Scholar 

  • Grau J, Schwab A (1982) Mikromerkmale der Blüte zur Gliederung der Gattung Myosotis. Mitt Bot Staatssamml München 18:8–58

    Google Scholar 

  • Guindon S, Gascuel O (2003) A simple, fast and accurate method to estimate large phylogenies by maximum-likelihood. Syst Biol 52:696–704

    Article  PubMed  Google Scholar 

  • Gürke (1893) Boraginaceae In: Engler, Prantl (eds) Nat Pflanzenfam, pp 71–131

  • Gussarova G, Popp M, Vitek E, Brochmann C (2008) Molecular phylogeny and biogeography of the bipolar Euphrasia (Orobanchaceae): Recent radiations in and old genus. Molec Phylogenet Evol 48:444–460

    Article  CAS  PubMed  Google Scholar 

  • Hasenstab-Lehman KE, Simpson MG (2012) Cat’s eyes and popcorn flowers: Phylogenetic systematics of the genus Cryptantha s.l. (Boraginaceae). Syst Bot 37:738–757

    Article  Google Scholar 

  • Heenan PB, McGlone MS (2013) Evolution of New Zealand alpine and open-habitat plant species during the late Cenozoic. New Zealand J Ecol 37:105–113

    Google Scholar 

  • Hilger HH, Selvi F, Papini A, Bigazzi M (2004) Molecular systematics of Boraginaceae tribe Boragineae based on ITS1 and trnL sequences, with special reference to Anchusa s.l. Ann Bot (Oxford) 94:201–212

    Article  CAS  Google Scholar 

  • Hollis CJ, Beu AG, Crampton JS, Crundwell MP, Morgans HEG, Raine JI, Jones CM, Boyes AF (2010) Calibration of the New Zealand Cretaceous-Cenzoic timescale to GTS2004. GNS Sci Rep 43:1–20

    Google Scholar 

  • Ho SYW, Phillips MJ (2009) Accounting for calibration uncertainty in phylogenetic estimation of evolutionary divergence times. Syst Biol 58:367–380

    Article  PubMed  Google Scholar 

  • Howarth DG, Baum DA (2002) Phylogenetic utility of a nuclear intron from nitrate reductase for the study of closely related plant species. Molec Phylogenet Evol 23:525–528

    Article  CAS  PubMed  Google Scholar 

  • Huson DH, Bryant D (2006) Application of phylogenetic networks in evolutionary studies. Molec Biol Evol 23:254–267

    Article  CAS  PubMed  Google Scholar 

  • Jesson LK (2007) Ecological correlates of diversification in New Zealand angiosperm lineages. New Zealand J Bot 45:35–51

    Article  Google Scholar 

  • Joly S, Heenan PB, Lockhart PJ (2009) A Pleistocene inter-tribal allopolyploidization event precedes the species radiation of Pachycladon (Brassicaceae) in New Zealand. Molec Phylogenet Evol 51:365–372

    Article  CAS  PubMed  Google Scholar 

  • Joly S, Heenan PB, Lockhart PJ (2014) Species radiation by niche shifts in New Zealand’s rockcresses (Pachycladon, Brassicaceae). Syst Biol 63:192–202

    Article  PubMed  Google Scholar 

  • Khoshsokhan Mozaffar M, Kazempour Osaloo S, Oskoueiyan R, Naderi Saffar K, Amirahmadi A (2013) Tribe Eritrichieae (Boraginaceae s. str.) in West Asia: a molecular phylogenetic perspective. Pl Syst Evol 299:197–208

    Article  Google Scholar 

  • Kolarčik V, Zozomová-Lihová J, Mártonfi P (2010) Systematics and evolutionary history of the Asterotricha group of the genus Onosma (Boraginaceae) in central and southern Europe inferred from AFLP and nrDNA ITS data. Pl Syst Evol 290:21–45

    Article  Google Scholar 

  • Långström E, Chase MW (2002) Tribes of Boraginoideae (Boraginaceae) and placement of Antiphytum, Echiochilon, Ogastemma and Sericostoma: a phylogenetic analysis based on atpB plastid DNA sequence data. Pl Syst Evol 234:137–153

    Article  Google Scholar 

  • Långström E, Oxelman B (2003) Phylogeny of Echiochilon (Echiochileae, Boraginaceae) based on ITS sequences and morphology. Taxon 52:725–735

    Article  Google Scholar 

  • Lee WG, Tanentzap AJ, Heenan PB (2012) Plant radiation history affects community assembly: evidence from the New Zealand alpine. Biol Lett. doi:10.1098/rsbl20111210

  • Lehnebach CA (2008) Phylogenetic affinities, species delimitation and adaptive radiation of New Zealand Ranunculus. Dissertation, Massey University, Palmerston North, New Zealand

  • Lehnebach CA (2012) Two new species of forget-me-nots (Myosotis, Boraginaceae) from New Zealand. PhytoKeys 16:53–64. doi:10.3897/phytokeys163602

    Article  PubMed  Google Scholar 

  • Levin RA, Blanton J, Miller JS (2009) Phylogenetic utility of nuclear nitrate reductase: A multi-locus comparison of nuclear and chloroplast sequence data for inference of relationships among American Lycieae (Solanaceae). Molec Phylogenet Evol 50:608–617

    Article  CAS  PubMed  Google Scholar 

  • Li M, Wunder J, Bissoli G, Scarponi E, Gazzani S, Barbaro E, Saedler H, Varotto C (2008) Development of COS genes as universally amplifiable markers for phylogenetic reconstructions of closely related plant species. Cladistics 24:727–745

    Article  Google Scholar 

  • Lockhart PJ, McLenachan PA, Havell D, Glenny D, Huson D, Jensen U (2001) Phylogeny, radiation, and transoceanic dispersal of New Zealand alpine buttercups: molecular evidence under split decomposition. Ann Missouri Bot Gard 88:458–477

    Article  Google Scholar 

  • Mabberley DJ (2008) Mabberley’s Plant-book, 3rd edn. Cambridge University Press, Cambridge

    Google Scholar 

  • Mandáková T, Heenan PB, Lysak MA (2010) Island species radiation and karyotypic stasis in Pachycladon allopolyploids. BMC Evol Biol 10:367

  • Mansion G, Selvi F, Guggisberg A, Conti E (2009) Origin of Mediterranean insular endemics in the Boraginales: Integrative evidence from molecular dating and ancestral area reconstruction. J Biogeogr 36:1282–1296

    Article  Google Scholar 

  • Meudt HM (2006) A monograph of the genus Ourisia Comm. ex Juss. (Plantaginaceae). Syst Bot Monogr 77:1–188

    Google Scholar 

  • Meudt HM (2008) Taxonomic revision of Australasian snow hebes (Veronica, Plantaginaceae). Austral Syst Bot 21:387–421

    Article  Google Scholar 

  • Meudt HM (2011) Amplified fragment length polymorphism data reveal a history of auto- and allopolyploidy in New Zealand endemic species of Plantago (Plantaginaceae): new perspectives on a taxonomically challenging group. Int J Pl Sci 172:220–237

    Article  Google Scholar 

  • Meudt HM (2012) A taxonomic revision of native New Zealand Plantago (Plantaginaceae). New Zealand J Bot 50:101–178

    Article  Google Scholar 

  • Meudt HM, Bayly MJ (2008) Phylogeographic patterns in the Australasian genus Chionohebe (Veronica s.l., Plantaginaceae) based on AFLP and chloroplast DNA sequences. Molec Phylogenet Evol 47:319–338

    Article  CAS  PubMed  Google Scholar 

  • Meudt HM, Lockhart PJ, Bryant D (2009) Species delimitation and phylogeny of a New Zealand plant species radiation. BMC Evol Biol 9:111

    Article  PubMed Central  PubMed  Google Scholar 

  • Meudt HM, Prebble JM, Stanley RC, Thorsen MJ (2013) Morphological and amplified fragment length polymorphism (AFLP) data show that New Zealand endemic Myosotis petiolata (Boraginaceae) comprises three rare and threatened species. Austral Syst Bot 26:210–232

  • Mitchell AD, Heenan PB, Murray BG, Molloy BPJ, de Lange PJ (2009) Evolution of the south-western Pacific genus Melicytus (Violaceae): evidence from DNA sequence data, cytology and sex expression. Austral Syst Bot 22:143–157

    Article  CAS  Google Scholar 

  • Moore LB (1961) Boraginaceae. In: Allan HH (ed) Flora of New Zealand. PD Hasselberg, Government printer Wellington, pp 806–833

    Google Scholar 

  • Moore MJ, Jansen RK (2006) Molecular evidence for the age, origin, and evolutionary history of the American desert plant genus Tiquilia (Boraginaceae). Molec Phylogenet Evol 39:668–687

    Article  CAS  PubMed  Google Scholar 

  • Moore LB, Simpson JA (1973) A new Myosotis from north-west Nelson. New Zealand J Bot 11:163–170

    Article  Google Scholar 

  • Murray B, de Lange PJ (2013) Contributions to a chromosome atlas of the New Zealand flora – 40 miscellaneous counts for 36 families. New Zealand J Bot 51:31–60

    Article  Google Scholar 

  • Nazaire M, Wang XQ, Hufford L (2014) Geographic origins and patterns of radiation of Mertensia (Boraginaceae). Amer J Bot 101:104–118

    Article  Google Scholar 

  • Nazaire M, Hufford L (2012) A broad phylogenetic analysis of Boraginaceae: implications for the relationships of Mertensia. Syst Bot 37:758–783

    Article  Google Scholar 

  • Peralta IE, Spooner DM (2001) Granule-bound starch synthase (GBSSI) gene phylogeny of wild tomatoes (Solanum L. section Lycopersicon [Mill.] Wettst. subsection Lycopersicon). Amer J Bot 88:1888–1902

    Article  CAS  Google Scholar 

  • Pirie MD, Lloyd KM, Lee WG, Linder HP (2010) Diversification of Chionochloa (Poaceae) and biogeography of the New Zealand Southern Alps. J Biogeogr 37:379–392

    Article  Google Scholar 

  • Prebble JM, Meudt HM, Garnock-Jones PJ (2012) An expanded molecular phylogeny of the southern bluebells (Wahlenbergia, Campanulaceae) from Australia and New Zealand. Austral Syst Bot 25:11–30

    Article  Google Scholar 

  • Rambaut A, Drummond AJ (2007) Tracer v16. Available from http://www.beastbioedacuk/Tracer

  • Rambaut A, Drummond AJ (2010) LogCombiner v1 54 MCMC Output Combiner. University of Edinburgh, Institute of Evolutionary Biology

    Google Scholar 

  • Rambaut A, Drummond AJ (2013) TreeAnnotator v1 70. University of Edinburgh, Institute of Evolutionary Biology

    Google Scholar 

  • Robertson AW (1989) Evolution and pollination of New Zealand Myosotis (Boraginaceae). Dissertation, University of Canterbury, Christchurch

  • Robertson AW (1992) The relationship between floral display size, pollen carryover and geitonogamy in Myosotis colensoi (Kirk) Macbride (Boraginaceae). Biol J Linn Soc 46:333–349

    Article  Google Scholar 

  • Robertson AW, MacNair MR (1995) The effects of floral display size on pollinator service to individual flowers of Myosotis and Mimulus. Oikos 72:106–114

    Article  Google Scholar 

  • Rogers G, Walker S, Tubbs M, Henderson J (2002) Ecology and conservation status of three “spring annual” herbs in dryland ecosystems of New Zealand. New Zealand J Bot 40:649–669

    Article  Google Scholar 

  • Segal R (1966) Taxonomic study of the fossil species of the genus Cryptantha (Boraginaceae). Southwest Nat 11:205–210

    Article  Google Scholar 

  • Schmidt-Lebuhn AN, Kessler M, Kumar M (2006) Promiscuity in the Andes: species relationships in Polylepis (Rosaceae, Sanguisorbeae) based on AFLP and morphology. Syst Bot 31:547–559

    Article  Google Scholar 

  • Shaw J, Lickey EB, Beck JT, Farmer SB, Liu W, Miller J, Siripun KC, Winder CT, Schilling EE, Small RL (2005) The tortoise and the hare II: relative utility of 21 noncoding chloroplast DNA sequences for phylogenetic analysis. Amer J Bot 92:142–166

    Article  CAS  Google Scholar 

  • Shaw J, Lickey EB, Schilling EE, Small RL (2007) Comparison of whole chloroplast genome sequences to choose noncoding regions for phylogenetic studies in angiosperms: the tortoise and the hare III. Amer J Bot 94:275–288

    Article  CAS  Google Scholar 

  • Skinner MF, Johnson FW (1984) Tertiary stratigraphy and the Frick collection of fossil vertebrates from north-central Nebraska. Bull Amer Museum Nat Hist 178:215–368

    Google Scholar 

  • Smissen RD, Galbany-Casals M, Breitwieser I (2011) Ancient allopolyploidy in the everlasting daisies (Asteraceae: Gnaphalieae): Complex relationships among extant clades. Taxon 60:649–662

    Google Scholar 

  • Smissen RD, Morse CW, Prada D, Ramón-Laca A, Richardson SJ (2012) Characterisation of seven polymorphic microsatellites for Nothofagus subgenus Fuscospora from New Zealand. New Zealand J Bot 50:227–231

    Article  Google Scholar 

  • Stamatakis A (2006) RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics 22:2688–2690

    Article  CAS  PubMed  Google Scholar 

  • Stanley RJ, Dickinson KJM, Mark AF (1998) Demography of a rare endemic Myosotis: boom and bust in the high-alpine zone of southern New Zealand. Arctic Alpine Res 30:227–240

    Article  Google Scholar 

  • Steele PR, Guisinger-Bellian M, Linder CR, Jansen RK (2008) Phylogenetic utility of 141 low-copy nuclear regions in taxa at different taxonomic levels in two distantly related families of rosids. Molec Phylogenet Evol 48:1013–1026

    Article  CAS  PubMed  Google Scholar 

  • Valdés B (2004) The Euro + Med treatment of Boraginaceae. Willdenowia 34:59–61

    Article  Google Scholar 

  • Wagstaff SJ, Bayly MJ, Garnock-Jones PJ, Albach DC (2002) Classification, origin and diversification of the New Zealand hebes (Scrophulariaceae). Ann Missouri Bot Gard 89:38–63

    Article  Google Scholar 

  • Wagstaff SJ, Breitwieser I (2004) Phylogeny and classification of Brachyglottis (Senecioneae, Asteraceae): An example of a rapid species radiation in New Zealand. Syst Bot 29:1003–1010

    Article  Google Scholar 

  • Wagstaff SJ, Garnock-Jones PJ (2000) Patterns and diversification of Chionohebe and Parahebe (Scrophulariaceae) inferred from ITS sequences. New Zealand J Bot 38:389–407

    Article  Google Scholar 

  • Webb CJ, Sykes WR, Garnock-Jones PJ (1988) Flora of New Zealand, vol IV. DSIR, Christchurch

    Google Scholar 

  • Weeks A, Simpson BB (2004) Molecular genetic evidence for interspecific hybridization among endemic Hispaniolan Bursera (Burseraceae). Amer J Bot 91:976–984

    Article  CAS  Google Scholar 

  • Weigend M, Gottschling M, Selvi F, Hilger HH (2009) Marbleseeds are gromwells—systematics and evolution of Lithospermum and allies (Boraginaceae tribe Lithospermeae) based on molecular and morphological data. Molec Phylogenet Evol 52:755–768

    Article  PubMed  Google Scholar 

  • Weigend M, Gottschling M, Selvi F, Hilger HH (2010) Fossil and extant western hemisphere Boragineae, and the polyphyly of “Trigonotideae” Riedl. (Boraginaceae: Boraginoideae). Syst Bot 35:409–419

    Article  Google Scholar 

  • Weigend M, Luebert F, Selvi F, Brokamp G, Hilger HH (2013) Multiple origins for hound’s tongues (Cynoglossum L.) and navel seeds (Omphalodes Mill.)–The phylogeny of the borage family (Boraginaceae s. str.). Molec Phylogenet Evol 68:604–618

    Article  PubMed  Google Scholar 

  • White TJ, Bruns T, Lee S, Taylor J (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics In: Innis, MA, Gelfand, DH, Sninsky, JJ, and White, TJ, (eds), PCR Protocols: a guide to methods and applications. Academic Press, Inc., pp 315–322

  • Winkworth RC, Grau J, Robertson AW, Lockhart PJ (2002) The origins and evolution of the genus Myosotis L. (Boraginaceae). Molec Phylogenet Evol 24:180–193

    Article  PubMed  Google Scholar 

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Acknowledgments

We would like to thank Pat Brownsey and Ilse Breitwieser for their support of this project, staff from AK, CHR and WELT, the Department of Conservation (DOC) for permission and help to collect samples on DOC land, the many colleagues who helped with field work and sample collection (especially John Barkla, Andrea Brandon, Fiona Cameron, Hamish Carson, Bill Clarkson, Shannel Courtney, Pat Enright, Phil Garnock-Jones, David Glenny, Ant Kusabs, Alan Lee, Mike Lusk, Viv McGlynn, Brian Rance, Nick Singers, Jorge Santos, Barry Sneddon, Bec Stanley, Mike Thorsen, Steve Wagstaff, and Andreas Zeller), Dirk Albach, Dick Olmstead, and Matt Renner for sending Boraginaceae outgroup tissue and DNA, Peter Ritchie for use of the Molecular Ecology lab at Victoria University of Wellington to generate the DNA sequence and AFLP data, Simon Pfanzelt for key discussions and unwavering help running BEAST analyses, Phil Garnock-Jones for commenting on an earlier version of the manuscript, and two anonymous reviewers for their highly constructive criticisms during the review process. We acknowledge use of information contained in the New Zealand Fossil Record File. This research was supported by Core funding for Crown Research Institutes from the Ministry of Business, Innovation and Employment’s Science and Innovation Group.

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  1. Museum of New Zealand Te Papa Tongarewa, PO Box 467, Cable St, Wellington, 6140, New Zealand

    Heidi M. Meudt, Jessica M. Prebble & Carlos A. Lehnebach

  2. School of Biological Sciences, Victoria University of Wellington, Wellington, 6140, New Zealand

    Heidi M. Meudt & Carlos A. Lehnebach

  3. Institute of Fundamental Sciences, Massey University, Private Bag 11222, Palmerston North, 4442, New Zealand

    Jessica M. Prebble

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  1. Heidi M. Meudt
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Correspondence to Heidi M. Meudt.

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606_2014_1166_MOESM1_ESM.pdf

Online Resource 1 Table showing voucher details including GenBank accession numbers. ITS sequences downloaded from GenBank include a reference; all other sequences were newly sequenced for this study. Author names are given for species, subspecies and varieties not listed in Table 1 (PDF 150 kb)

606_2014_1166_MOESM2_ESM.pdf

Online Resource 2 RAxML phylogram of combined nuclear (ITS + ETS) DNA sequence dataset; scale units are substitutions per site. Individual names are genus + species epithet + Genbank number for the atpI–atpH sequence (or if no atpI–atpH sequence, then Genbank number for the ITS sequence). Numbers above branches are bootstrap values from 1000 replicates. L, C and M indicate the location of the calibration points based on Lithospermum, Cryptantha and New Zealand Myosotis fossils respectively (note these are shown here for illustrative purposes only as they were used in the BEAST analyses not in this RAxML anlaysis; see text for details). Voucher information for all individuals is given in Online Resource 1 (PDF 978 kb)

606_2014_1166_MOESM3_ESM.pdf

Online Resource 3 RAxML phylogram of combined chloroplast DNA (rps16-trnQ+atpI–atpH intergenic spacer regions) dataset; scale units are substitutions per site. Individual names are genus + species epithet + Genbank number for the atpI–atpH sequence (or if no atpI–atpH sequence, then Genbank number for the ITS sequence). Numbers above branches are bootstrap values from 1000 replicates. Voucher information for all individuals is given in Online Resource 1 (PDF 526 kb)

606_2014_1166_MOESM4_ESM.pdf

Online Resource 4 BEAST chronogram of combined nuclear (ITS + ETS) DNA sequence dataset using Lithospermum (L) and Cryptantha (C) fossil calibration points with uniform priors (the Myosotis fossil calibration point [M] was not used in this analysis; see text for details). The scale line is in millions of years before present. Individual names are genus + species epithet + Genbank number for the atpI–atpH sequence (or if no atpI–atpH sequence, then Genbank number for the ITS sequence). Dark circles signify branches with posterior probability values >0.95. Voucher information for all individuals is given in Online Resource 1 (PDF 49 kb)

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Meudt, H.M., Prebble, J.M. & Lehnebach, C.A. Native New Zealand forget-me-nots (Myosotis, Boraginaceae) comprise a Pleistocene species radiation with very low genetic divergence. Plant Syst Evol 301, 1455–1471 (2015). https://doi.org/10.1007/s00606-014-1166-x

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