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RESEARCH ARTICLE

Floral morphology and pollination system in the native Australian perennial pasture legume Cullen australasicum (syn. Psoralea australasica)

Yan-Jing Wang A , Ramakrishnan M. Nair B C E , Chun-Sheng Mu A and Ian S. Dundas D
+ Author Affiliations
- Author Affiliations

A Institute of Grassland Science, Northeast Normal University, Key Laboratory of Vegetation Ecology, Ministry of Education, Changchun, Jilin Province 130024, China.

B South Australian Research and Development Institute, GPO Box 397, Adelaide, SA 5001, Australia.

C Future Farm Industries Cooperative Research Centre, The University of Western Australia, 35 Stirling Highway, Crawley, WA 6009, Australia.

D School of Agriculture and Wine, University of Adelaide, Waite Campus, PMB 1, Glen Osmond, SA 5064, Australia.

E Corresponding author. Email: ramakrishnanmnair@gmail.com

Crop and Pasture Science 61(12) 1001-1008 https://doi.org/10.1071/CP10193
Submitted: 2 June 2010  Accepted: 1 November 2010   Published: 8 December 2010

Abstract

Cullen australasicum (syn. Psoralea australasica) is a native perennial legume with potential in the low-rainfall wheatbelt of southern Australia. The objective of this study was to investigate the reproductive biology of C. australasicum utilising five accessions. Glasshouse and field pollination experiments were conducted in Adelaide, South Australia. Floral morphology, stigma receptivity and pollen : ovule ratios were determined. Pollen tube growth and stigma morphology were examined using fluorescence and scanning electron microscopes. Glasshouse pollination studies indicated that four of the accessions showed the need for an external tripping agent to bring about pollination and that hand-tripping was the most efficient method. A scanning electron microscopy study revealed there are two types of stigmas in this species. Stigma receptivity was significantly lower at the early bud stage before anther dehiscence. The results show that C. australasicum is a self-compatible species comprising accessions with a wide range of outcrossing potential.

Additional keywords: pollen tube growth, stigmatic surface cuticle.


References

Allard RW (1960) ‘Principles of plant breeding.’ (John Wiley & Sons, Inc.: New York)

Armstrong JM, White WJ (1935) Factors influencing seed-setting in alfalfa. The Journal of Agricultural Science 25, 161–179.
Factors influencing seed-setting in alfalfa.Crossref | GoogleScholarGoogle Scholar |

Britten EJ, Dundas IS (1985) A dimorphic pollination system in a potentially valuable semi-arid pasture legume, the Psoralea patens complex. In ‘Proceedings of the 15th International Grassland Congress’. Kyoto, Japan. pp. 209–210. (Science Council of Japan and Japan Society of Grassland Science: Kyoto)

Charlesworth D (1988) A method for estimating outcrossing rates in natural populations of plants. Heredity 61, 469–471.
A method for estimating outcrossing rates in natural populations of plants.Crossref | GoogleScholarGoogle Scholar |

Charlesworth D, Charlesworth B (1987) Inbreeding depression and its evolutionary consequences. Annual Review of Ecology and Systematics 18, 237–268.
Inbreeding depression and its evolutionary consequences.Crossref | GoogleScholarGoogle Scholar |

Cruden RW (1977) Pollen–ovule ratios: a conservative indicator of breeding systems in flowering plants. Evolution 31, 32–46.
Pollen–ovule ratios: a conservative indicator of breeding systems in flowering plants.Crossref | GoogleScholarGoogle Scholar |

Dafni A, Maués MM (1998) A rapid and simple procedure to determine stigma receptivity. Sexual Plant Reproduction 11, 177–180.
A rapid and simple procedure to determine stigma receptivity.Crossref | GoogleScholarGoogle Scholar |

Dear BS, Li GD, Hayes RC, Hughes SJ, Charman N, Ballard RA (2007) Cullen australasicum (Syn. Psoralea australasica): a review and some preliminary studies related to its potential as a low rainfall perennial pasture legume. The Rangeland Journal 29, 121–132.
Cullen australasicum (Syn. Psoralea australasica): a review and some preliminary studies related to its potential as a low rainfall perennial pasture legume.Crossref | GoogleScholarGoogle Scholar |

Dear BS, Reed KFM, Craig AD (2008) Outcomes of the search for new perennial and salt tolerant pasture plants for southern Australia. Australian Journal of Experimental Agriculture 48, 578–588.
Outcomes of the search for new perennial and salt tolerant pasture plants for southern Australia.Crossref | GoogleScholarGoogle Scholar |

Dobson AJ (2002) ‘An introduction to generalized linear models.’ 2nd edn (Chapman & Hall/CRC: Boca Raton, FL)

Galloni M, Podda L, Vivarelli D, Cristofolini G (2007) Pollen presentation, pollen-ovule ratios, and other reproductive traits in Mediterranean legumes (Fam. Fabaceae-Subfam. Faboideae). Plant Systematics and Evolution 266, 147–164.
Pollen presentation, pollen-ovule ratios, and other reproductive traits in Mediterranean legumes (Fam. Fabaceae-Subfam. Faboideae).Crossref | GoogleScholarGoogle Scholar |

Gibbs P, Sassaki R (1998) Reproductive biology of Dalbergia miscolobium Benth. (Leguminosae-Papilionoideae) in SE Brazil: the effects of pistillate sorting on fruit-set. Annals of Botany 81, 735–740.
Reproductive biology of Dalbergia miscolobium Benth. (Leguminosae-Papilionoideae) in SE Brazil: the effects of pistillate sorting on fruit-set.Crossref | GoogleScholarGoogle Scholar |

Gori DF (1989) Floral color change in Lupinus argenteus (Fabaceae): why should plants advertise the location of unrewarding flowers to pollinators? Evolution 43, 870–881.
Floral color change in Lupinus argenteus (Fabaceae): why should plants advertise the location of unrewarding flowers to pollinators?Crossref | GoogleScholarGoogle Scholar |

Greyson RI, Tepfer SS (1967) Emasculation effects on the stamen filament of Nigella hispanica and their partial reversal by gibberellic acid. American Journal of Botany 54, 971–976.
Emasculation effects on the stamen filament of Nigella hispanica and their partial reversal by gibberellic acid.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF1cXitFCl&md5=d0f9698d8d6e3e1556f4ae8415701faeCAS |

Grimes JW (1997) A revision of Cullen (Leguminosae: Papilionoideae). Australian Systematic Botany 10, 565–648.
A revision of Cullen (Leguminosae: Papilionoideae).Crossref | GoogleScholarGoogle Scholar |

Hayes RC, Li GD, Dear BS, Humphries AW, Tidd JR (2009) Persistence, productivity, nutrient composition, and aphid tolerance of Cullen spp. Crop & Pasture Science 60, 1184–1192.
Persistence, productivity, nutrient composition, and aphid tolerance of Cullen spp.Crossref | GoogleScholarGoogle Scholar |

Hedhly A, Hormaza JI, Herrero M (2009) Flower emasculation accelerates ovule degeneration and reduces fruit set in sweet cherry. Scientia Horticulturae 119, 455–457.
Flower emasculation accelerates ovule degeneration and reduces fruit set in sweet cherry.Crossref | GoogleScholarGoogle Scholar |

Heslop-Harrison J, Heslop-Harrison Y (1985) Surfaces and secretions in the pollen-stigma interaction: a brief review. Journal of Cell Science. Supplement 2, 287–300.

Kittelson PM, Maron JL (2000) Outcrossing rate and inbreeding depression in the perennial yellow bush lupine, Lupinus arboreus (Fabaceae). American Journal of Botany 87, 652–660.
Outcrossing rate and inbreeding depression in the perennial yellow bush lupine, Lupinus arboreus (Fabaceae).Crossref | GoogleScholarGoogle Scholar | 10811789PubMed |

Kouonon LC, Jacquemart AL, Zoro Bi AI, Bertin P, Baudoin JP, Dje Y (2009) Reproductive biology of the andromonoecious Cucumis melo subsp. agrestis (Cucurbitaceae). Annals of Botany 104, 1129–1139.
Reproductive biology of the andromonoecious Cucumis melo subsp. agrestis (Cucurbitaceae).Crossref | GoogleScholarGoogle Scholar | 19671577PubMed |

Kreitner GL, Sorensen EL (1984) Stigma development and the stigmatic cuticle of alfalfa, Medicago sativa L. Botanical Gazette 145, 436–443.
Stigma development and the stigmatic cuticle of alfalfa, Medicago sativa L.Crossref | GoogleScholarGoogle Scholar |

Kroiss L, Moody M, Barker S, Byrne M, Ryan M (2009) Development, characterization and transferability of microsatellite markers for Cullen australasicum (Leguminosae). Conservation Genetics 10, 1803–1805.
Development, characterization and transferability of microsatellite markers for Cullen australasicum (Leguminosae).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhsFSrtLfN&md5=d6273c175d245cd434d6f2b646231077CAS |

Lloyd DG, Schoen DJ (1992) Self-and cross-fertilization in plants. I. Functional dimensions. International Journal of Plant Sciences 153, 358–369.
Self-and cross-fertilization in plants. I. Functional dimensions.Crossref | GoogleScholarGoogle Scholar |

Lord EM, Heslop-Harrison Y (1984) Pollen-stigma interaction in the Leguminosae: stigma organization and the breeding system in Vicia faba L. Annals of Botany 54, 827–836.

Lord EM, Webster BD (1979) The stigmatic exudate of Phaseolus vulgaris L. Botanical Gazette 140, 266–271.
The stigmatic exudate of Phaseolus vulgaris L.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE1MXmtVOntbo%3D&md5=6bd186c26a7e09ed9a7edff268dff373CAS |

Lynch M (1991) The genetic interpretation of inbreeding depression and outbreeding depression. Evolution 45, 622–629.
The genetic interpretation of inbreeding depression and outbreeding depression.Crossref | GoogleScholarGoogle Scholar |

Matkin OA, Chandler PA (1957) ‘The UC type soil mixes.’ Section 5 in California Agricultural Experiment Station Manual 23. (University of California: Berkeley, CA)

Mustajärvi K, Siikamäki P, Akerberg A (2005) Inbreeding depression in perennial Lychnis viscaria (Caryophyllaceae): effects of population mating history and nutrient availability. American Journal of Botany 92, 1853–1861.
Inbreeding depression in perennial Lychnis viscaria (Caryophyllaceae): effects of population mating history and nutrient availability.Crossref | GoogleScholarGoogle Scholar |

Nair RM, Dundas IS, Wallwork M, Verlin DC, Waterhouse L, Dowling K (2004) Breeding system in a population of Trigonella balansae (Leguminosae). Annals of Botany 94, 883–888.
Breeding system in a population of Trigonella balansae (Leguminosae).Crossref | GoogleScholarGoogle Scholar | 15489252PubMed |

Percival MS (1979) ‘Floral biology.’ 3rd edn (Pergamon Press Ltd: Oxford, UK)

Richards AJ (1997) ‘Plant breeding systems.’ (Chapman and Hall: London)

Sahai K (2009) Reproductive biology of two species of Canavalia DC. (Fabaceae) – a non-conventional wild legume. Flora – Morphology, Distribution, Functional Ecology of Plants 204, 762–768.
Reproductive biology of two species of Canavalia DC. (Fabaceae) – a non-conventional wild legume.Crossref | GoogleScholarGoogle Scholar |

Sharma AK, Sharma A (1980) ‘Chromosome techniques, theory and practice.’ 3rd edn (Butterworths: London)

Sigrist MR, Sazima M (2004) Pollination and reproductive biology of twelve species of neotropical Malpighiaceae: stigma morphology and its implications for the breeding system. Annals of Botany 94, 33–41.
Pollination and reproductive biology of twelve species of neotropical Malpighiaceae: stigma morphology and its implications for the breeding system.Crossref | GoogleScholarGoogle Scholar | 15194562PubMed |

Small E, Crompton CW, Brookes BS (1981) The taxonomic value of floral characters in tribe Trigonelleae (Leguminosae), with special reference to Medicago. Canadian Journal of Botany 59, 1578–1598.

Small E, Lassen P, Brookes BS (1987) An expanded circumscription of Medicago (Leguminosae, Trifolieae) based on explosive flower tripping. Willdenowia 16, 415–437.

Vogler DM, Kalisz S (2001) Sex among the flowers: the distribution of plant mating systems. Evolution 55, 202–204.

Weiss MR (1995) Floral color change: a widespread functional convergence. American Journal of Botany 82, 167–185.
Floral color change: a widespread functional convergence.Crossref | GoogleScholarGoogle Scholar |

Weiss MR, Lamont BB (1997) Floral color change and insect pollination: a dynamic relationship. Israel Journal of Plant Sciences 45, 185–199.

Wyatt R (1983) Pollinator-plant interactions and the evolution of breeding systems. Pollination Biology 51, 51–95.