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 CA 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.
Allan, HH (1961).
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.
Oliver WRB
(1935) The genus Coprosma. Bernice P.
Bishop Museum Bulletin 132, 1–207.
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 |
Richard, A (1832).
Sale, EV (1978).
Schwarzacher, T ,
and
Heslop-Harrison, JS (2000).
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.
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 |
Thompson J
(1983) Redefinitions and nomenclatural changes within the Leptospermum suballiance of Myrtaceae. Telopea 2, 379–383.
Webb, CJ ,
and
Simpson, MJA (2001).
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)