Floral ontogeny of Hardenbergia violacea (Fabaceae: Faboideae: Phaseoleae) and taxa of tribes Bossiaeeae and Mirbelieae, with emphasis on presence of pseudoraceme inflorescences
Shirley C. TuckerDepartment of Ecology, Evolution and Marine Biology, University of California, Santa Barbara, California 93106-9610, USA, and Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana 70803, USA. Email: tucker@lifesci.ucsb.edu
Australian Systematic Botany 19(3) 193-210 https://doi.org/10.1071/SB05004
Submitted: 17 March 2005 Accepted: 13 December 2005 Published: 30 June 2006
Abstract
The floral ontogeny of several Australian papilionoid taxa has been studied in Hardenbergia violacea L. (Phaseoleae); Kennedia rubicunda (Phaseoleae; inflorescences only); Bossiaea cordigera (Bossiaeeae); Gastrolobium truncatum, Mirbelia oxylobioides, and Pultenaea daphnoides (Mirbelieae). Species studied of Hardenbergia, Pultenaea, and Brachysema have pseudoracemose inflorescences comprised of triads of flowers, Kennedia rubicunda has paired flowers that resemble reduced pseudoracemes, while Gastrolobium truncatum and Mirbelia oxylobioides have pseudoracemes comprised of 2–10 flowers per ultimate unit. Pseudoracemes are a significant and overlooked feature in many taxa of tribes Bossiaeeae and Mirbelieae. Hardenbergia violacea has ultimate axillary units of three flowers, each with a subtending bract but no bracteoles. Floral ontogeny in H. violacea and P. daphnoides shows acropetal order among whorls, and unidirectional order starting from the abaxial side in sepal, petal, and stamen whorls, as in most papilionoid flowers. The carpel is initiated concurrently with the first antesepalous stamen primordium. Pultenaea daphnoides and Bossiaea cordigera have unidirectional sepal initiation starting abaxially, but simultaneous petal initiation, an unusual feature among papilionoids. In late stages of H. violacea and B. cordigera, a diadelphous stamen tube or sheath is formed, while in taxa of Mirbelieae the stamens remain free. The flowers in all taxa studied become strongly zygomorphic as evidenced by three petal morphs and upturning of the free portions of style and stamens late in development.
Acknowledgments
I thank Jo Anna Bass and David Pierce for their technical assistance with scanning electron microscopy and photography, and Jan Beckert for drawings. Permission to collect material at the Arboretum of the University of California, Santa Cruz, CA, is acknowledged and appreciated. Scanning electron microscopy work was done at the Electron Microscopy facility at the Department of Geology, University of California, Santa Barbara, California 93106, USA. The research was supported by Boyd Professorship funds from Louisiana State University, Baton Rouge, Louisiana.
Berg RY
(1979) Legume, seed, and myrmechorous dispersal in Kennedia and Hardenbergia (Fabaceae), with a remark on the Durian theory. Norwegian Journal of Botany 26, 229–254.
Briggs BG, Johnson LAS
(1979) Evolution in the Myrtaceae—evidence from inflorescence structure. Proceedings of the Linnean Society of New South Wales 102, 157–272.
Crisp MD, Cook LG
(2003b) Molecular evidence for definition of genera in the Oxylobium group (Fabaceae: Mirbelieae). Systematic Botany 28, 705–713.
Crozier TS, Thomas JF
(1993) Normal floral ontogeny and cool temperature-induced aberrant floral development in Glycine max (Fabaceae). American Journal of Botany 80, 429–448.
| Crossref |
Guard AT
(1931) Development of floral organs of the soybean. Botanical Gazette 91, 97–102.
| Crossref | GoogleScholarGoogle Scholar |
Hirsch AM,
Krupp RSN,
Lin Y,
Wang SW,
Yang W, Tucker SC
(2002) Inflorescence and flower development in wild-type and sid mutant in Melilotus alba. Canadian Journal of Botany 80, 732–740.
| Crossref | GoogleScholarGoogle Scholar |
Horner HT,
Healy RA,
Cervantes-Martinez T, Palmer RG
(2003) Floral nectary fine structure and development in Glycine max L. (Fabaceae). International Journal of Plant Sciences 164, 675–690.
| Crossref | GoogleScholarGoogle Scholar |
Johnson LAS
(1976) Problems of species and genera in Eucalyptus (Myrtaceae). Plant Systematics and Evolution 125, 155–167.
| Crossref |
Kajita T,
Ohashi H,
Tateishi Y,
Bailey CD, Doyle JJ
(2001) RbcL and legume phylogeny, with particular reference to Phaseoleae, Millettieae, and allies. Systematic Botany 26, 515–536.
Klitgaard BB
(1999) Floral ontogeny of four taxa of Dalbergieae. Plant Systematics and Evolution 219, 1–25.
| Crossref | GoogleScholarGoogle Scholar |
Mair O
(1977) Zur Entwicklungsgeschichte monosymmetrischer Dicotylen-Blüten. Dissertationes Botanicae 38, 1–90, 260–274.
Prenner G
(2004a) The asymmetric androecium in Papilionoideae (Leguminosae): definition, occurrence, and possible systematic value. International Journal of Plant Sciences 165, 499–510.
| Crossref | GoogleScholarGoogle Scholar |
Prenner G
(2004b) Floral development in Daviesia cordata (Leguminosae: Papilionoideae: Mirbelieae) and its systematic implications. Australian Journal of Botany 52, 285–291.
| Crossref | GoogleScholarGoogle Scholar |
Prenner G
(2004c) Floral ontogeny in Lespedeza thunbergii (Leguminosae: Papilionoideae: Desmodieae): variations from the unidirectional mode of organ formation. Journal of Plant Research 117, 297–302.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Rohrbach P
(1870) Beiträge zur Morphologie der Leguminosen. Botanisches Zeitschrift 28, 817–829.
Sands VE
(1975) The cytoevolution of the Australian Papilionaceae. Proceedings of the Linnean Society of New South Wales 100, 118–155.
Tucker SC
(1984) Unidirectional organ initiation in leguminous flowers. American Journal of Botany 71, 1139–1148.
| Crossref |
Tucker SC
(1987a) Pseudoracemes in papilionoid legumes: their nature, development, and variation. Botanical Journal of the Linnean Society of London 95, 181–206.
Tucker SC
(1989) Overlapping organ initiation and common primordia in flowers of Pisum sativum (Leguminosae: Papilionoideae). American Journal of Botany 76, 714–729.
| Crossref |
Tucker SC
(1993) Floral ontogeny in Sophoreae (Leguminosae: Papilionoideae). l. Myroxylon (Myroxylon group) and Castanospermum (Angylocalyx group). American Journal of Botany 80, 65–75.
| Crossref |
Tucker SC
(1994) Floral ontogeny in Sophoreae (Leguminosae: Papilionoideae). II. Sophora (Sophora group). American Journal of Botany 81, 368–380.
| Crossref |
Tucker SC
(1997) Floral evolution, development, and convergence: the hierarchical-significance hypothesis. International Journal of Plant Sciences 158, S143–S161.
| Crossref | GoogleScholarGoogle Scholar |
Tucker SC
(2002) Floral ontogeny in Sophoreae (Leguminosae: Papilionoideae). III. Cadia purpurea with radial symmetry and random petal aestivation. American Journal of Botany 89, 748–757.
Tucker SC
(2003) Floral development in legumes. Update on floral development. Plant Physiology 131, 911–926.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Tucker SC, Stirton CH
(1991) Development of the cymose inflorescence, cupulum, and flower of Psoralea pinnata (Leguminosae: Papilionoideae: Psoraleeae). Botanical Journal of the Linnean Society of London 106, 208–227.
Tucker SC, Kantz KE
(2001) Open carpels with ovules in Fabaceae. International Journal of Plant Sciences 162, 1065–1073.
| Crossref | GoogleScholarGoogle Scholar |
Waddle RM, Lersten NR
(1974) Morphology of discoid floral nectaries in Leguminosae, especially tribe Phaseoleae (Papilionoideae). Phytomorphology 23, 152–161.
Wojciechowski MF,
Lavin M, Sanderson MJ
(2004) A phylogeny of legumes (Leguminosae) based on analysis of the plastid matK gene resolves many well-supported subclades within the family. American Journal of Botany 91, 1846–1862.