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

Hybridism in the Kunzea ericoides complex (Myrtaceae): an analysis of artificial crosses

P. J. de Lange A D , P. M. Datson B , B. G. Murray B and H. R. Toelken C
+ Author Affiliations
- Author Affiliations

A Terrestrial Conservation Unit, Department of Conservation, Private Bag 68908, Newton, Auckland, New Zealand.

B School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland, New Zealand.

C State Herbarium of South Australia, P O Box 2732, Kent Town, SA 5071, Australia.

D Corresponding author. Email: pdelange@doc.govt.nz

Australian Systematic Botany 18(2) 117-131 https://doi.org/10.1071/SB04043
Submitted: 10 November 2004  Accepted: 10 March 2005   Published: 20 May 2005

Abstract

Observations of wild plants and herbarium specimens suggest that hybridism is a feature of the Australasian Kunzea ericoides (Myrtaceae) complex. In this study 73 artificial cross combinations were attempted with New Zealand material of Leptospermum scoparium, five Kunzea species, two varieties and six informally recognised entities within the New Zealand K. ericoides complex. The results of these crosses are documented, and for five hybrids spanning the intergeneric, interspecific and intraspecific crosses attempted, we provide a more detailed assessment based on morphology, molecular (nrDNA and chloroplast) sequence variation, and genomic in situ hybridisation (GISH). This is the first time GISH has been used in the Myrtaceae. Hybrids were easily generated between the New Zealand members of the K. ericoides complex, but not between them and the Australian K. ericoides complex. We were unable to produce hybrids between the New Zealand K. ericoides complex and two more distantly related Australian species, K. baxteri and K. parvifolia. Intergeneric crosses between New Zealand plants of Leptospermum scoparium, Kunzea sinclairii and an informally recognised variant K. aff. ericoides (b) were successfully produced, but failed to flower. The molecular evidence and observations after GISH show that even when low levels of sequence divergence exist, genome differentiation, to different extents, can be observed. The results confirm some suspected New Zealand hybrid complexes. However, while hybrids were easily generated artificially, natural instances of hybridism appear to be largely confined to those habitats significantly disturbed since European settlement of both countries.


Acknowledgments

This paper is dedicated to the memory of the late J. S. Holloway, former Director, Science & Research Unit, New Zealand Department of Conservation, whose life was tragically cut short by illness. We thank S. Beadel, P. Cashmore, G. Davidson, C. Ecroyd, L. J. Forester, D. Gosling, T. Myers, N. Head, P. Knightbridge, B. P. J. Molloy, C. C. Ogle, G. Platt, J. W. D. Sawyer, N. J. Singers, M. J. Thorsen and A. J. Townsend, for the provision of live plants or specimens of various members of the New Zealand K. ericoides complex, permits, transport and/or field assistance. D. Cameron (Department of Sustainability and Environment, Arthur Rylah Institute, Victoria, Australia) assisted with permits, transport and field collection of the K. ericoides complex in Victoria, Australia. For discussion and comments received on earlier versions of the manuscript we are grateful to M. Bayly, P. B. Heenan, G. M. Crowcroft, W. Harris, D. A. Norton, J. Salter and R. Stanley. D. J. Keeling, assisted with DNA sequencing and GenBank accessioning. J. Salter prepared the figures. M. Lee (AK) assisted with herbarium searches and accessioning. Lastly, we acknowledge D. G. Newman, (Manager, Terrestrial Conservation Unit, New Zealand Department of Conservation) for his long-term support of this study.


References


Allan, HH (1961). ‘Flora of New Zealand.’ Vol. I. (Government Printer: Wellington)

Andras SC, Hartman TPV, Marshall JA, Marchant R, Power JB, Cocking EC, Davey MR (1999) A drop-spreading technique to produce cytoplasm-free mitotic preparations from plants with small chromosomes. Chromosome Research 7, 641–647.
Crossref | GoogleScholarGoogle Scholar | (School of Health Science, Griffith University, Gold Coast Campus, South Port, Queensland)

Murray BG, Datson PM, Lai ELY, Sheath KM, Cameron EK (2004) Polyploidy, evolution and hybridisation in Pratia (Campanulaceae). New Zealand Journal of Botany 42, 905–920. open url image1

Oliver WRB (1935) The genus Coprosma. Bernice P.  Bishop Museum Bulletin 132, 1–207. open url image1

Osuji JO, Harrison G, Crouch J, Heslop-Harrison JS (1997) Identification of the genomic constitution of Musa L. lines (bananas, plantains and hybrids) using molecular cytogenetics. Annals of Botany 80, 787–793.
Crossref | GoogleScholarGoogle Scholar | open url image1

Richard, A (1832). ‘Essai d’une Flore de La Nouvelle Zélande.’ : Paris)

Sale, EV (1978). ‘Quest for the kauri: forest giants and where to find them.’ (Reed: Wellington)

Schwarzacher, T ,  and  Heslop-Harrison, JS (2000). ‘Practical hybridization.’ (BIOS Scientific Publishers Limited: Oxford)

Schwarzacher T, Leitch AR, Bennett MD, Heslop-Harrison JS (1989) In situ localization of parental genomes in a wide hybrid. Annals of Botany 64, 315–324. open url image1

Taberlet P, Gielly L, Pautou G, Bouvet J (1991) Universal primers for amplification of three non-coding regions of chloroplast DNA. Plant Molecular Biology 17, 1105–1109.
Crossref | GoogleScholarGoogle Scholar | open url image1

Thompson J (1983) Redefinitions and nomenclatural changes within the Leptospermum suballiance of Myrtaceae. Telopea 2, 379–383. open url image1

Webb, CJ ,  and  Simpson, MJA (2001). ‘Seeds of New Zealand gymnosperms and dicotyledons.’ (Manuka Press: Christchurch)

White, T , Bruns, T , Lee, S ,  and  Taylor, J (1990). Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In ‘PCR protocols: a guide to methods and applications’. pp. 315–322. (Academic Press: San Diego)