Floral development of Najas flexilis

1976 ◽  
Vol 54 (10) ◽  
pp. 1140-1151 ◽  
Author(s):  
U. Posluszny ◽  
R. Sattler

Two subopposite leaves form at a node. The lower one arises almost simultaneously with the axillary meristem which it subtends. The upper leaf initiates after the lower one and does not subtend any structure. The axillary meristem gives rise to a renewal growth apex and a floral bud almost at its inception. In some cases the axillary meristem forms only a floral bud. The floral bud may be either staminate or pistillate. The main axis and the renewal growth in the axil of the lower leaf repeat this pattern of development. Staminate and pistillate flowers are almost indistinguishable at inception. They form as dome-like protuberances and both initiate girdling primordia, which become lobed at or immediately after inception. In the staminate flower the girdling primordium becomes the outer envelope, while a second girdling primordium formed acropetally becomes the inner envelope. Both envelopes overgrow the one-celled anther, which is the transformed staminate floral apex. In the pistillate flower the girdling primordium becomes the gynoecial wall that encloses the single bitegmic ovule, which is the transformed pistillate floral apex. On a short style a stigma with two to four branches develops. The renewal growth apices have a one-layered tunica. The two subopposite leaves are initiated through cell division in both tunica and corpus cells. The axillary meristem arises through periclinal divisions in the corpus cells. The girdling primordia of both staminate and pistillate floral buds are epidermal in origin as are the integuments of the ovule. Procambial development is acropetal following closely primordia inception. Each leaf, floral bud, and renewal growth apex receives a single strand. No vascularization is seen in envelopes of the staminate flower or the gynoecial wall of the pistillate flower, all of which remain two cell layers thick even at maturity.

1976 ◽  
Vol 54 (8) ◽  
pp. 651-662 ◽  
Author(s):  
U. Posluszny ◽  
R. Sattler

What, at maturity, appears to be a bisexual flower in the axil of one of two subopposite leaves, is revealed as a fertile nodal complex with quite different organization. Three appendages develop at each nodal complex. The first girdles the stem and becomes at maturity a membranous sheath about the entire node. The second subtends the axillary meristem, which terminates as the staminate flower, and branches laterally as a renewal growth in the axil of a sterile appendage just below the stamen. The third appendage is subopposite the terminal meristem, which gives rise to the pistillate floral bud towards the staminate flower, and a renewal growth apex towards the appendage. This renewal growth apex repeats the entire pattern at almost a 90° shift to the right or left, depending on the shoot. The single stamen of the staminate flower develops as those studied in Potamogeton and Ruppia. The pistillate flower develops two carpel primordia, which become peltate before initiating a single ovule primordium on the adaxial portion (Querzone). The membranous envelope which covers the carpels at maturity is initiated at ovule inception, below one of the carpels. A peltate stigma differentiates on a short style and at maturity becomes broad and lobed. The renewal growth apex has a one-layered tunica. The membranous sheaths of the node and of the pistillate flower are primarily protodermal in origin, while the rest of the sterile and reproductive appendages arise through activity in subprotodermal cells. Procambial development is acropetal closely following primordial inception. Each organ (sterile or fertile) receives one procambial strand, except for the membranous sheath about the node and the one about the pistillate flower.


1974 ◽  
Vol 52 (7) ◽  
pp. 1607-1612 ◽  
Author(s):  
U. Posluszny ◽  
R. Sattler

A hyaline, unvascularized sheath envelops a portion of the inflorescence near maturity. Though resembling an appendage of the main axis, in early ontogeny it develops as a prophyll of the renewal growth apex below the inflorescence. Two flowers develop on the inflorescence axis, subopposite each other. Fertile appendages are initiated in an acropetal sequence on each floral bud. The first to form, in the median position, are the two stamens, the lower preceding the upper. Each stamen develops two bisporangiate thecae separated by a broad connective. A dorsiventral outgrowth is initiated slightly abaxially near the tip of the connective at the stage of theca differentiation. This outgrowth appears to be homologous with a similar outgrowth in Potamogeton densus, but not with the sterile appendages of the Potamogeton flower which, by some authors, have incorrectly been interpreted as connective outgrowths. Each carpel arises as a radial primordium which becomes peltate after its inception. One ovule is initiated at the adaxial portion (Querzone). The stigma becomes broad and flat, lobing at its margins. A slight outgrowth develops at the abaxial wall of the carpel. The floral apex has a two-layered tunica. The primordia of the stamens, carpels, and ovules arise by periclinal divisions in the second layer. Procambial development is acropetal following closely primordial inception. Each appendage, including the ovule, receives one procambial strand. The outgrowths of the connective and the carpel lack procambium.


PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e2811 ◽  
Author(s):  
Arthur de Lima Silva ◽  
Marcelo Trovó ◽  
Alessandra Ike Coan

BackgroundFlowers in Eriocaulaceae, a monocot family that is highly diversified in Brazil, are generally trimerous, but dimerous flowers occur inPaepalanthusand a few other genera. The floral merism in an evolutionary context, however, is unclear.Paepalanthusencompasses significant morphological variation leading to a still unresolved infrageneric classification. Ontogenetic comparative studies of infrageneric groups inPaepalanthusand in Eriocaulaceae are lacking, albeit necessary to establish evolution of characters such as floral merism and their role as putative synapomorphies.MethodsWe studied the floral development and vascularization of eight species ofPaepalanthusthat belong to distinct clades in which dimery occurs, using light and scanning electron microscopies.ResultsFloral ontogeny in dimerousPaepalanthusshows lateral sepals emerging simultaneously and late-developing petals. The outer whorl of stamens is absent in all flowers examined here. The inner whorl of stamens becomes functional in staminate flowers and is reduced to staminodes in the pistillate ones. In pistillate flowers, vascular bundles reach the staminodes. Ovary vascularization shows ventral bundles in a commissural position reaching the synascidiate portion of the carpels. Three gynoecial patterns are described for the studied species: (1) gynoecium with a short style, two nectariferous branches and two long stigmatic branches, in most species; (2) gynoecium with a long style, two nectariferous branches and two short stigmatic branches, inP. echinoides; and (3) gynoecium with long style, absent nectariferous branches and two short stigmatic branches, inP. scleranthus.DiscussionFloral development of the studied species corroborates the hypothesis that the sepals of dimerous flowers ofPaepalanthuscorrespond to the lateral sepals of trimerous flowers. The position and vascularization of floral parts also show that, during dimery evolution inPaepalanthus, a flower sector comprising the adaxial median sepal, a lateral petal, a lateral stamen and the adaxial median carpel was lost. In the staminate flower, the outer whorl of staminodes, previously reported by different authors, is correctly described as the apical portion of the petals and the pistillodes are reinterpreted as carpellodes. The occurrence of fused stigmatic branches and protected nectariferous carpellodes substantiates a close relationship betweenP.sect.ConodiscusandP.subg.Thelxinoë. Free stigmatic branches and exposed carpellodes substantiate a close relationship betweenP. sect.Diphyomene,P. sect.EriocaulopsisandP. ser.Dimeri. Furthermore, the loss of nectariferous branches may have occurred later than the fusion of stigmatic branches in the clade that groupsP. subg.ThelxinoëandP. sect.Conodiscus.


1997 ◽  
Vol 75 (1) ◽  
pp. 145-154 ◽  
Author(s):  
Naida L. Lehmann ◽  
Rolf Sattler

Development of staminate flowers in double-flowering Begonia semperflorens-cultorum cultivars 'Cinderella', 'Goldie Locks', and 'Lucy Lockett' was examined using epi-illumination microscopy, focussing on later stages when secondary partial floral buds formed on the floral apex. This process, switching from floral to inflorescence-like development, is an example of homeosis, the expression of inflorescence features on a floral apex. Floral development began as in a normal begonia flower with the formation of a perianth consisting of two sepals and two petals, but sepaloid and (or) petaloid appendages then developed in what corresponded to stamen positions in normal Begonia species. This was usually followed by lateral elongation, distortion of the primary floral apex, and formation of secondary partial floral buds. The pattern of primordial inception on the secondary apices tended to be irregular, but in some cases, appendage primordia formed in groups of twos, threes, and fours, and in a somewhat alternating formation on the apices. Often, primordial initiation seemed to continue on secondary apices even after anthesis of the staminate flower. Appendage primordia that formed on the secondary buds usually were laterally elongate and bifacial, giving them a phyllomic appearance. Others were, on occasion, more hemispherical at inception, but as they developed they became phyllomic. Key words: homeosis, polyaxial, floral development, intermediate inflorescence.


2015 ◽  
Vol 33 (4) ◽  
pp. 453-458 ◽  
Author(s):  
Tania P Silva ◽  
Fernando L Finger

ABSTRACT: This work describes ethylene and 1-methylcyclopropene (1-MCP) action on post-harvest shelf life of four development stages of nasturtium flowers. To reach this goal, we carried out three experiments. In the first and second experiments, we studied five ethylene (0; 0.1; 1; 10; 100 and 1000 μL/L) and three 1-MCP concentrations (0.25; 0.5 and 0.75 μL/L), respectively. In the third experiment, 1-MCP was followed by combined with ethylene (only 1-MCP; only ethylene; and 24 hours of exposure to 0.75 μL/L 1-MCP followed by 24 hours of exposure to 100 μL/L ethylene). All experiments had two control treatments, one keeping non-exposed flowers inside and another outside exposure chambers. Experiments were set in factorial design, in complete blocks at random, with four 10-flower replications each. Flower senescence was determined by a pre-established visual scale and by observing floral bud development. Ethylene dose above 10 μL/L induced flower wilting and premature senescence from the second floral development stage. Furthermore, higher concentrations of exogenous ethylene promoted irregular flower opening and/or morphological abnormalities in opened flowers. 1-MCP effectively extended post-harvest longevity of nasturtium flowers, independent of the concentration and even in the presence of exogenous ethylene.


Development ◽  
2000 ◽  
Vol 127 (6) ◽  
pp. 1267-1276 ◽  
Author(s):  
P.D. Jenik ◽  
V.F. Irish

The shoot apical meristem of Arabidopsis thaliana consists of three cell layers that proliferate to give rise to the aerial organs of the plant. By labeling cells in each layer using an Ac-based transposable element system, we mapped their contributions to the floral organs, as well as determined the degree of plasticity in this developmental process. We found that each cell layer proliferates to give rise to predictable derivatives: the L1 contributes to the epidermis, the stigma, part of the transmitting tract and the integument of the ovules, while the L2 and L3 contribute, to different degrees, to the mesophyll and other internal tissues. In order to test the roles of the floral homeotic genes in regulating these patterns of cell proliferation, we carried out similar clonal analyses in apetala3-3 and agamous-1 mutant plants. Our results suggest that cell division patterns are regulated differently at different stages of floral development. In early floral stages, the pattern of cell divisions is dependent on position in the floral meristem, and not on future organ identity. Later, during organogenesis, the layer contributions to the organs are controlled by the homeotic genes. We also show that AGAMOUS is required to maintain the layered structure of the meristem prior to organ initiation, as well as having a non-autonomous role in the regulation of the layer contributions to the petals.


1992 ◽  
Vol 70 (2) ◽  
pp. 258-271 ◽  
Author(s):  
Claudia Erbar

The early floral development of Stylidium adnatum and Stylidium graminifolium is characterized by an initial circular primordium whose areas in the transversal plane of the floral primordium show enhanced growth. The spiral inception of the five sepals starts before the differentiation of the initial circular primordium into two stamen primordia in transversal position (in relation to the floral diagram) and the corolla ring primordium below the stamen primordia. Then five petal primordia, which alternate with the sepals, arise on the corolla ring primordium (early sympetaly). Peculiar to the flowers of Stylidiaceae is the column that bears at its top both stigma and anthers. Probably this column should be interpreted as a receptacular tube. No distinct carpel primordia have been observed. The inferior ovary results from intercalary growth in the peripheral parts of the receptacle below the calyx, corolla, and stamen primordia. The residual floral apex gives rise to a transversal septum, by which the ovary becomes bilocular. None of the morphological, palynological, and embryological characters discussed contradicts a position of the Stylidiaceae near the Campanulales, and several of these characters support this position. Key words: Stylidiaceae, Campanulales, floral development, systematic position, floral biology.


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