Molecular phylogeny of the suspended aquatic Utricularia (sect. Utricularia) with a new hybrid species U. × jacobsii from northern Australia, a new section Biovularia, and confirmation of two species in New Zealand
DOI:
https://doi.org/10.7751/telopea19758Keywords:
Utricularia, BladderwortAbstract
Utricularia sect. Utricularia contains 35 recognised species world-wide, including the recently described U. adamsii from northern Australia. We here present a molecular phylogeny of subgenus Utricularia representing most Australian species based on sequences of two plastid markers and nuclear ITS. We provide molecular evidence for hybridization events between U. aurea and U. muelleri that have occurred sporadically across northern Australia. We found phylogenetic discordance between the plastid and nuclear sequences for two of the suspected hybrid specimens. The morphological differences between U. muelleri, U. aurea and the hybrid taxon are discussed with a formal description of the hybrid taxon presented as Utricularia × jacobsii R.W.Jobson & Baleeiro. We also provide molecular evidence for the introduction/naturalization of northeastern USA/Canada endemic U. geminiscapa into New Zealand (NZ) and confirm that a NZ accession of U. australis is most closely related to those U. australis populations distributed in south-eastern Australia. We expand the section Avesicaria to include the taxa in sections Setiscapella and Steyermarkia. Lastly, we recognise a new sectional name Biovularia (Kamieński) Baleeiro & R.W.Jobson for U. olivacea. that was found to be excluded from sect. Utricularia and instead is supported as a close ally to sect. Vesiculina.
References
Astuti G, Petroni G, Adamec L, Miranda VFO, Peruzzi L (2020) DNA barcoding approach fails to discriminate Central European bladderworts (Utricularia, Lentibulariaceae), but provides insights concerning their evolution. Plant Biosystems 154: 326–336. https://doi.org/10.1080/11263504.2019.1610112
Baleeiro P, Jobson RW, Sano P (2016) Morphometric approach to address taxonomic problems: The case of Utricularia sect. Foliosa (Lentibulariaceae). Journal of Systematics & Evolution 54: 175–186. https://doi.org/10.1111/jse.12186
Baleeiro P, Sano P, Jobson RW (2019) Molecular phylogeny of the Utricularia amethystina complex (Sect. Foliosa) addressed using plastid and nuclear sequences data. Systematic Botany 2: 398–404. https://doi.org/10.1600/036364419X15562052252045
Baleeiro PC, Sano P, Gonella P, Jobson RW (2022) Unveiling the true colours of Utricularia amethystina: a taxonomic revision of U. sect. Foliosa, Lentibulariaceae. Phytotaxa 576: 29–54. https://doi.org/10.11646/phytotaxa.576.1.2
Barnhart JH (1915) Segregation of genera in the Lentibulariaceae. Memoirs of the New York Botanical Garden 6: 39–64
Beal EO, Quay TL (1968) A review of Utricularia olivacea Wright ex Grisebach (Lentibulariaceae). Journal of the Elisha Mitchell Scientific Society 84: 462–466.
Bobrov AA, Volkova PA, Kopylov-Guskov YO, Mochalova OA, Kravchuk AE, Nekrasova DM (2022) Unknown sides of Utricularia (Lentibulariaceae) diversity in East Europe and North Asia or how hybridization explained old taxonomical puzzles. Perspectives in Plant Ecology, Evolution and Systematics 54: 1–19. https://doi.org/10.1016/j.ppees.2021.125649
Champion P, Hofstra D (20242). Utricularia geminiscapa. NIWA publication. https://www.nzpcn.org.nz/flora/species/utricularia-geminiscapa/
Guindon S, Gascuel O (2003) A simple, fast and accurate method to estimate large phylogenies by maximum likelihood. Systematic Biology 52: 696–704. https://doi.org/10.1080/10635150390235520
Heenan PB, de Lange PJ, Knightsbridge PI (2004) Utricularia geminiscapa (Lentibulariaceae), a naturalised aquatic bladderwort in the South Island, New Zealand. New Zealand Journal of Botany 24: 247–251. https://doi.org/10.1080/0028825X.2004.9512901
Jobson RW (2012) Utricularia corneliana R.W.Jobson (Lentibulariaceae), a new species from the North Kennedy district of Queensland. Austrobaileya 8: 601–607. https://doi.org/10.5962/p.299822
Jobson RW, Albert VA (2002) Molecular rates parallel diversification contrasts in carnivorous plant sister lineages. Cladistics 18: 127–136. https://doi.org/10.1006/clad.2001.0187
Jobson RW, Baleeiro PC (2020) Radiations of fairy-aprons (Utricularia dichotoma, Lentibulariacceae) across eastern Australia: molecular evidence for new species and proposal for new subspecies. Australian Systematic Botany 33: 278–310. https://doi.org/10.1071/sb19003
Jobson RW, Baleeiro PC (2022) Rescircumscription of Utricularia leptorhyncha and U. lasiocaulis and three related new species for northern Australia. Telopea 25: 363–383. https://doi.org/10.7751/telopea16750
Jobson RW, Baleeiro PC (2023). Molecular phylogenetic study of Utricularia section Oligocista in Australia and a new Cape York endemic species. Telopea 26: 145–158 https://doi.org/10.7751/telopea17500
Jobson RW, Baleeiro PC, Guisande C (2018) Systematics and evolution of Lentibulariaceae: III. Utricularia, Pg. 89–104, In Ellison A, Adamec L (Eds) Carnivorous plants: physiology, ecology, and evolution. Oxford University Press: Oxford.
Jobson RW, Baleeiro P, Reut M. (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. https://doi.org/10.1071/SB17003
Jobson RW, Davies-Colley T (2020) Redescription of the suspended aquatic Utricularia aurea Lour. (sect. Utricularia) and a new species U. adamsii for northern Australia. Telopea 23: 21–33. https://doi.org/10.7751/telopea14301
Jobson RW, Playford J, Cameron KM, Albert VA (2003) Molecular phylogenetics of Lentibulariaceae inferred from plastid rps16 intron and trnL–F DNA sequences: implications for character evolution and biogeography. Systematic Botany 28: 157–171. https://doi.org/10.1043/0363-6445-28.1.157
Moar NT, Mason R (1975) Discovery of Utricularia protrusa Hook.f. near Westport, South Island, New Zealand. New Zealand Journal of Botany 13: 803–805. https://doi.org/10.1080/0028825X.1975.10430359
Müller K, Borsch T (2005) Phylogenetics of Utricularia (Lentibulariaceae) and molecular evolution of the trnK intron in a lineage with high substitutional rates. Plant Systematics and Evolution 250: 39–67. https://doi.org/10.1007/s00606-004-0224-1
Oxelman B, Lidén M, Berglund D (1997) Chloroplast rps16 intron phylogeny of the tribe Sileneae (Caryophyllaceae). Plant Systematics and Evolution 206: 393–410. https://doi.org/10.1007/BF00987959
Posada D (2008) jModelTest: phylogenetic model averaging. Molecular Biology and Evolution 25: 1253–1256. https://doi.org/10.1093/molbev/msn083
Robins RJ, Subramanyam K (1980) Scanning electron microscope study of the seed surface morphology of some Utricularia (Lentibulariaceae) species from India. Proceedings of the Indian National Science Academy 46B: 310–324.
Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Höhna S, Larget B, Liu L, Suchard MA, and Huelsenbeck JP (2012) MRBAYES 3.2: Efficient Bayesian phylogenetic inference and model selection across a large model space. Systematic Biology 61: 539–542. https://doi.org/10.1093/sysbio/sys029
Salmon B (2001) Carnivorous plants of New Zealand. Auckland, Ecosphere Publications.
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. https://doi.org/10.3732/ajb.92.1.142
Silva SR, Miranda VF, Michael TP, Płachno BJ, Matos RG, Adamec L, Pond SL, Lucaci AG, Pinheiro DG, Varani AM (2023) The phylogenomics and evolutionary dynamics of the organellar genomes in carnivorous Utricularia and Genlisea species (Lentibulariaceae). Molecular Phylogenetics and Evolution 181, 107711. https://doi.org/10.1016/j.ympev.2023.107711
Stanford AM, Harden R, Parks CR (2000) Phylogeny and biogeography of Juglans (Juglandaceae) based on matK and ITS sequence data. American Journal of Botany 87: 872–882. https://doi.org/10.2307/2656895
Taylor P (1989) The genus Utricularia. Kew Bulletin Additional Series 14. Royal Botanic Gardens: Kew.
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.
Downloads
Published
Issue
Section
License
Copyright (c) 2024 Richard W Jobson, Lesley F. Elkan, Paulo Baleeiro
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.