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Australian Systematic Botany Australian Systematic Botany Society
Taxonomy, biogeography and evolution of plants
RESEARCH ARTICLE

Radiations of fairy-aprons (Utricularia dichotoma, Lentibulariaceae) in Australia and New Zealand: molecular evidence and proposal of new subspecies

Richard W. Jobson https://orcid.org/0000-0002-1822-9634 A C and Paulo C. Baleeiro B
+ Author Affiliations
- Author Affiliations

A National Herbarium of New South Wales, Royal Botanic Garden, Sydney, Mrs Macquaries Road, Sydney, NSW 2000, Australia.

B School of Biological Sciences, The University of Queensland, Brisbane, Qld 4072, Australia.

C Corresponding author. Email: richard.jobson@rbgsyd.nsw.gov.au

Australian Systematic Botany 33(3) 278-310 https://doi.org/10.1071/SB19003
Submitted: 22 January 2019  Accepted: 20 September 2019   Published: 19 February 2020

Abstract

The Utricularia dichotoma Labill. complex is a morphologically and ecologically variable group of closely related taxa with a mostly temperate distribution across New Zealand, New Caledonia and Australia. Taxonomic boundaries within the complex have been the subject of speculation, with several previously recognised species being synonymised after a nomenclatural revision. We sampled 296 populations representing all known taxa; 223 accessions were used in the full phylogenetic analysis based on two non-coding chloroplast regions (rps16, trnD–T) and two nuclear ribosomal spacers (external transcribed spacer, ETS; internal transcribed spacer-1, ITS-1), whereas the remaining accessions were identified by using ITS-1 barcodes. We found strong support for a paraphyletic U. dichotoma, with accessions matching the type material of that name grouped within a polytomy that includes clades containing accessions of U. monanthos Hook.f and U. novae-zelandiae Hook.f. Specific statuses for five recently described species previously included in U. dichotoma s.l. do not fall within this polytomy, nor do the two species U. oppositiflora R.Br. and U. speciosa R.Br. resurrected from synonymy of U. dichotoma. All sampled accessions from New Zealand form a single clade within U. dichotoma as recognised here. We here propose that seven clades recovered here be recognised as subspecies, and describe eight new subspecies, including two new combinations. We also propose that the monophyletic clade sister to U. beaugleholei Gassin be assigned to subspecies rank under that name.


References

Anon. (2014) Advisory list of rare or threatened plants in Victoria. Department of Environment and Primary Industries, State Government of Victoria, Melbourne, Vic., Australia. Available at https://www.environment.vic.gov.au/__data/assets/pdf_file/0021/50448/Advisory-List-of-Rare-or-Threatened-Plants-in-Victoria-2014.pdf [Verified 25 October 2018].

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). Molecular Phylogenetics and Evolution 10, 449–463.
Phylogenetic utility of the external transcribed spacer (ETS) of 18S-26S rDNA: congruence of ETS and ITS trees of Calycadenia (Compositae).Crossref | GoogleScholarGoogle Scholar | 10051397PubMed |

Bell DM, Hunter JT, Haworth RJ (2008) Montane lakes (lagoons) of the New England Tablelands Bioregion. Cunninghamia 10, 475–492.

Bentham G (1868) ‘Flora Australiensis’, vol. 4. p. 528. (Reeve: London, UK)

Brown R (1810) ‘Prodromus floræ Novæ Hollandiæ et Insulæ Van-Diemen: exhibens characteres plantarum quas annis 1802–1805.’ (R. Taylor et socii: London, UK)

de Lange PJ, Rolfe JR, Champion PD, Courtney SP, Heenan PB, Barkla JW, Cameron EK, Norton DA, Hitchmough RA (2013) ‘Conservation status of New Zealand indigenous Vascular Plants, 2012. Threat Classification Series 3.’ (Department of Conservation: Wellington, New Zealand)

Edgar C (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Research 32, 1792–1797.
MUSCLE: multiple sequence alignment with high accuracy and high throughput.Crossref | GoogleScholarGoogle Scholar |

Farris JS, Kallersjo M, Kluge AG, Bult C (1994) Testing the significance of incongruence. Cladistics 10, 315–319.
Testing the significance of incongruence.Crossref | GoogleScholarGoogle Scholar |

Gassin R (1993) Utricularia beaugleholei (Lentibulariaceae: subgenus Utricularia: section Pleiochasia), a new species from south-eastern Australia. Muelleria 8, 37–42.

Guindon S, Gascuel O (2003) A simple, fast and accurate method to estimate large phylogenies by maximum-likelihood. Systematic Biology 52, 696–704.
A simple, fast and accurate method to estimate large phylogenies by maximum-likelihood.Crossref | GoogleScholarGoogle Scholar | 14530136PubMed |

Hall TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series 41, 95–98.

Jobson RW (2012) A new species of Utricularia (Lentibulariaceae) from northern Queensland, Australia. Telopea 14, 49–57.
A new species of Utricularia (Lentibulariaceae) from northern Queensland, Australia.Crossref | GoogleScholarGoogle Scholar |

Jobson RW (2013) Five new species of Utricularia (Lentibulariaceae) from Australia. Telopea 15, 127–142.
Five new species of Utricularia (Lentibulariaceae) from Australia.Crossref | GoogleScholarGoogle Scholar |

Jobson RW, Baleeiro PC (2015) Two new species of Utricularia (Lentibulariaceae) from the North West region of Western Australia. Telopea 18, 201–208.
Two new species of Utricularia (Lentibulariaceae) from the North West region of Western Australia.Crossref | GoogleScholarGoogle Scholar |

Jobson RW, Playford J, Cameron KM, Albert VA (2003) Molecular phylogeny of Lentibulariaceae inferred from plastid rps16 intron and trnL–F DNA sequences: implications for character evolution and biogeography. Systematic Botany 28, 157–171.
Molecular phylogeny of Lentibulariaceae inferred from plastid rps16 intron and trnL–F DNA sequences: implications for character evolution and biogeography.Crossref | GoogleScholarGoogle Scholar |

Jobson RW, Baleeiro PC, Reut MS (2017) Molecular phylogeny of subgenus Polypompholyx (Utricularia; Lentibulariaceae) based on three plastid markers: diversification and proposal for a new section. Australian Systematic Botany 30, 259–278.
Molecular phylogeny of subgenus Polypompholyx (Utricularia; Lentibulariaceae) based on three plastid markers: diversification and proposal for a new section.Crossref | GoogleScholarGoogle Scholar |

Kantvilas G (2007) Labillardière and the beginnings of botanical exploration in Tasmania. In ‘Rediscovering Recherche Bay’. (Eds J Mulvaney, H Tyndale-Biscoe) pp. 35–44. (Academy of the Social Sciences in Australia: Canberra, ACT, Australia)

Kearse M, Moir R, Wilson A, Stones-Havas S, Cheung M, Sturrock S, Buxton S, Cooper A, Markowitz S, Duran C, Thierer T, Ashton B, Meintjes P, Drummond A (2012) Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics 28, 1647–1649.
Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data.Crossref | GoogleScholarGoogle Scholar | 22543367PubMed |

Labillardière JJH (1804) ‘Novae Hollandiae Plantarum Specimen.’ (Ex typographia Dominæ Huzard: Paris, France)

Mabberley DJ, Moore DT, Wajer J (in press) ‘The Robert Brown Handbook: a Guide to the Life and Work of Robert Brown (1773–1858), Scottish Botanist.’ Regnum Vegetabile, Vol. 160. (Wiley)

Oxelman B, Lidén M, Berglund D (1997) Chloroplast rps16 intron phylogeny of the tribe Sileneae (Caryophyllaceae). Plant Systematics and Evolution 206, 393–410.
Chloroplast rps16 intron phylogeny of the tribe Sileneae (Caryophyllaceae).Crossref | GoogleScholarGoogle Scholar |

Posada D (2008) jModelTest: phylogenetic model averaging. Molecular Biology and Evolution 25, 1253–1256.
jModelTest: phylogenetic model averaging.Crossref | GoogleScholarGoogle Scholar | 18397919PubMed |

Reut MS, Fineran BA (1999) An evaluation of the taxonomy of Utricularia dichotoma Labill., U. monanthos Hook.f., and U. novae-zelandiae Hook.f. (Lentibulariaceae). New Zealand Journal of Botany 37, 243–255.
An evaluation of the taxonomy of Utricularia dichotoma Labill., U. monanthos Hook.f., and U. novae-zelandiae Hook.f. (Lentibulariaceae).Crossref | GoogleScholarGoogle Scholar |

Reut MS, Fineran BA (2000) Ecology and vegetative morphology of the carnivorous plant Utricularia dichotoma (Lentibulariaceae) in New Zealand. New Zealand Journal of Botany 38, 433–450.
Ecology and vegetative morphology of the carnivorous plant Utricularia dichotoma (Lentibulariaceae) in New Zealand.Crossref | GoogleScholarGoogle Scholar |

Reut MS, Jobson RW (2010) A phylogenetic study of subgenus Polypompholyx: a parallel radiation of Utricularia (Lentibulariaceae) throughout Australasia. Australian Systematic Botany 23, 152–161.
A phylogenetic study of subgenus Polypompholyx: a parallel radiation of Utricularia (Lentibulariaceae) throughout Australasia.Crossref | GoogleScholarGoogle Scholar |

Shaw J, Shafer HL, Leonard OR, Kovach MJ, Schorr M, Morris AB (2005) The tortoise and the hare II: relative utility of 21 noncoding chloroplast DNA sequences for phylogenetic analysis. American Journal of Botany 92, 142–166.
The tortoise and the hare II: relative utility of 21 noncoding chloroplast DNA sequences for phylogenetic analysis.Crossref | GoogleScholarGoogle Scholar | 21652394PubMed |

Swofford DL (2002) ‘PAUP*: Phylogenetic Analysis using Parsimony (* and Other Methods).’ (Sinauer Associates: Sunderland, MA, USA)

Taylor P (1989) ‘The Genus Utricularia. Kew Bulletin, Additional Series XIV.’ (HMSO: London, UK)

White TJ, Bruns T, Lee S, Taylor JW (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In ‘PCR Protocols: a Guide to Methods and Applications’. (Eds MA Innis, DH Gelfand, JJ Sninsky, TJ White) pp. 315–322. (Academic Press, Inc.: New York, NY, USA)