Morphological and anatomical development in the Vitaceae. VII. Floral development in Rhoicissus digitata with respect to other genera in the family

2004 ◽  
Vol 82 (2) ◽  
pp. 198-206 ◽  
Author(s):  
Jean M Gerrath ◽  
T Wilson ◽  
Usher Posluszny

This study forms part of our series of investigations on genera in the Vitaceae and is the first developmental study for the genus Rhoicissus. Vegetative and reproductive development of shoot apices of Rhoicissus digitata (L.f.) Gilg et Brandt were examined using epi-illumination light microscopy and scanning electron microscopy. Leaf-opposed tendrils or inflorescences, typical of the shoot architecture in the Vitaceae, were present at every node. Macroscopically, the shoot appears to grow either monopodially or sympodially. At the microscopic level, however, shoot development is sympodial; the shoot apical meristem bifurcates unequally, with the larger portion forming an uncommitted primordium, which will become either an inflorescence or a tendril, and the smaller portion (in the position of the axillary bud) forming the new shoot apical meristem. Floral primordia first initiate three sepals followed by a calyx ring on which the last two sepal primordia form. The five petals are initiated in a whorl followed by the five stamens in a petal-opposed position. There is no evidence of a common petal-stamen primordium in this species. The gy noecium is initiated as a ring primordium. Subsequently, the four ovules are initiated at the base of the two septa that grow out from the inner gynoecial wall. The nectary disc forms as an outgrowth of the gynoecium base. Mature flowers have greenish petals and a red nectariferous disc. Flowers are bisexual, and seed germination is approximately 63%. Unlike previous studies in Vitis and Parthenocissus, Rhoicissus appears to have few putatively derived floral developmental characters, which would support its relatively basal position in current phylogenies for the family.Key words: Vitaceae, morphology, development, shoot architecture, flower.


Development ◽  
1996 ◽  
Vol 122 (8) ◽  
pp. 2395-2403 ◽  
Author(s):  
B. Grbic ◽  
A.B. Bleecker

In this paper, we describe a late-flowering ecotype of Arabidopsis, Sy-0, in which the axillary meristems maintain a prolonged vegetative phase, even though the primary shoot apical meristem has already converted to reproductive development. This novel heterochronic shift in the development of axillary meristems results in the formation of aerial rosettes of leaves at the nodes of the primary shoot axis. We present evidence that the aerial-rosette phenotype arises due to the interaction between dominant alleles of two genes: ART, aerial rosette gene (on chromosome 5) and EAR, enhancer of aerial rosette (on chromosome 4): EAR has been tentatively identified as a new allele of the FRI locus. The possible role of these two genes in the conversion of shoot apical meristems to reproductive development is discussed.



Development ◽  
1992 ◽  
Vol 116 (2) ◽  
pp. 397-403 ◽  
Author(s):  
H. M. Ottoline Leyser ◽  
I. J. Furner

The shoot apical meristem of dicotyledonous plants is highly regulated both structurally and functionally, but little is known about the mechanisms involved in this regulation. Here we describe the genetic and phenotypic characterisation of recessive mutations at three loci of Arabidopsis thaliana in which meristem structure and function are disrupted. The loci are Clavata1 (Clv1), Fasciata1 (Fas1) and Fasciata2 (Fas2). Plants mutant at these loci are fasciated having broad, flat stems and disrupted phyllotaxy. In all cases, the fasciations are associated with shoot apical meristem enlargement and altered floral development. While all the mutants share some phenotypic features they can be divided into two classes. The pleiotropic fas1 and fas2 mutants are unable to initiate wild- type organs, show major alterations in meristem structure and have reduced root growth. In contrast, clv1 mutant plants show near wild-type organ phenotypes, more subtle changes in shoot apical meristem structure and wild-type root growth.



2006 ◽  
Vol 84 (5) ◽  
pp. 702-716 ◽  
Author(s):  
Trevor C. Wilson ◽  
Jean M. Gerrath ◽  
Usher Posluszny

Vegetative and floral development of Cyphostemma simulans (C.A. Small) Wild & Drummond, Cyphostemma juttae (Dinter & Gilg) Descoings, and Cyphostemma mappia (Lam) Galet were compared using epi-illumination light microscopy and paraffin sectioning. Cyphostemma simulans is a liana with leaf-opposed tendrils and inflorescences, which both arise from the shoot apical meristem, whereas the other two species are shrubs that lack tendrils and their main shoot terminates in an inflorescence. A shoot apical meristem of C. simulans can be overtopped by an inflorescence, making the architecture appear to develop like a sympodium, which is the architecture shared by the other two species. On the other hand, a terminal inflorescence of C. juttae or C. mappia can be placed in a leaf-opposed position by a precocious axillary branch, making the architecture appear to develop like a monopodium, which is the typical architecture of the Vitaceae. The floral development of all three species is similar in early ontogeny, except for a difference in calyx development between C. mappia and the other two species. Later developmental differences of the septum and gynoecium, in addition to flower colour and phenology, are distinct characteristics that distinguish flowers of each species. Therefore, this study is the first to demonstrate differences in the floral characteristics of Cyphostemma. In addition, it shows how each architecture type (monopodium or sympodium) can resemble the other and so provides stronger evidence about how the unique architecture of the Vitaceae has originated.





2005 ◽  
Vol 83 (4) ◽  
pp. 343-349 ◽  
Author(s):  
Vojislava Grbić

Axillary and floral meristems are shoot meristems that initiate postembryonically. In Arabidopsis, axillary meristems give rise to branches during vegetative development while floral meristems give rise to flowers during reproductive development. This review compares the development of these meristems from their initiation at the shoot apical meristem up to the establishment of their specific developmental fates. Axillary and floral meristems originate from lateral primordia that form at flanks of the shoot apical meristem. Initial development of vegetative and reproductive primordia are similar, resulting in the formation of a morphologically defined primordium partitioned into adaxial and abaxial domains. The adaxial primordial domain is competent to form a meristem, while the abaxial domain correlates with the formation of a leaf. This review proposes that all primordia partition into domains competent to form the meristem and the leaf. According to this model, a vegetative primordium develops as leaf-bias while a reproductive primordium develops as meristem-bias.Key words: SHOOTMERISTEMLESS, LATERAL SUPPRESSOR, AINTEGUMENTA, adaxial primordial domain, abaxial primordial domain, shoot morphogenesis.



2021 ◽  
Author(s):  
Bihai Shi ◽  
Amelia Felipo-Benavent ◽  
Guillaume Cerutti ◽  
Carlos Galvan-Ampudia ◽  
Lucas Jilli ◽  
...  

Growth at the shoot apical meristem (SAM) is essential for shoot architecture construction. The phytohormones gibberellins (GA) play a pivotal role in coordinating plant growth, but their role in the SAM remains mostly unknown. Here, we developed a ratiometric GA signalling biosensor by engineering one of the DELLA repressors, to suppress its master regulatory function in GA transcriptional responses while preserving its degradation upon GA sensing. We demonstrate that this novel degradation-based biosensor accurately reports on cellular changes in GA levels and perception during development. We used this biosensor to map GA signalling activity in the SAM. We show that high GA signalling is found primarily in cells located between organ primordia that are the precursors of internodes. By gain- and loss-of-function approaches, we further demonstrate that GAs regulate cell division plane orientation to establish the typical cellular organisation of internodes, thus contributing to internode specification in the SAM.



HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 488a-488
Author(s):  
Ramona A. Reiser ◽  
Robert W. Langhans

The release of latent buds (adaptive reiteration) and aerial shoot architecture of the rhizomatous calla lily plant has been researched for pot production. Rhizome mapping has explicitly shown vegetative and floral bud positioning in relation to tissue growth and expansion. Floral initiation normally occurred only on the mother portion of rhizomes. Gibberellic acid (GA3) application enhanced this phenomenon and caused initiation on daughter ramets. Bud excision performed at planting through Day 16 microscopically revealed lack of floral initiation in dissected meristems prior to planting, transition by Day 4, elongation beginning at Day 8 and `small to medium sized spadixes present by Day 12 and 16. Floral development was similar in treated and untreated primary buds, but delayed in secondary and tertiary buds with elongation occurring by Day 16. Pretreatment of GA3 prior to planting revealed spadix presence at Day 0. Floral development correlated with ramet size showed most flowers on largest ramets but formation on all sizes with GA3 treatment. GA3 also caused increased vegetative bud formation on rhizomes.



Development ◽  
1991 ◽  
Vol 112 (3) ◽  
pp. 891-898 ◽  
Author(s):  
E.E. Irish ◽  
T.M. Nelson

Vegetative growth in most lines of maize is terminated stage in development by the conversion of the shoot inflorescence, the tassel. The conversion from under developmental control, the basis of which is developmental potential of the shoot apical meristem stage at which it is determined to form a tassel. We culture, that meristems are not determined to form a vegetative nodes have been initiated. We also show separate, later event in the development of a maize stages can be distinguished in which the meristem is phyllotaxis of a tassel when cultured but develops that normally give rise to sets of florets.



PLoS Genetics ◽  
2020 ◽  
Vol 16 (4) ◽  
pp. e1008661 ◽  
Author(s):  
Hasthi Ram ◽  
Sudeep Sahadevan ◽  
Nittaya Gale ◽  
Monica Pia Caggiano ◽  
Xiulian Yu ◽  
...  


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