The flowers of Dichorisandra thyrsiflora (Commelinaceae) are monosymmetric and composed of three sepals, three petals, six stamens, and three connate carpels. The anthers are poricidal and possess a wall of five cell layers (tapetum included). This type of anther wall, not previously observed in the Commelinaceae, is developmentally derived from the monocotyledonous type via an additional periclinal division and the persistence of the middle layers through anther dehiscence. Secondary endothecial thickenings develop in the cells of the two middle layers only. The tapetum is periplasmodial and contains raphides. Microsporogenesis is successive and yields both decussate and isobilateral tetrads. Pollen is shed as single binucleate grains. The gynoecium is differentiated into a globose ovary, hollow elongate style, and trilobed papillate stigma. Each locule contains six to eight hemianatropous to slightly campylotropous crassinucellar ovules with axile (submarginal) placentation. The ovules are bitegmic with a slightly zig-zag micropyle. Megagametophyte development is of the Polygonum type. The mature megagametophyte consists of an egg apparatus and fusion nucleus; the antipodals having degenerated. The floral vasculature is organized into an outer and inner system of bundles in the pedicel. The outer system becomes ventral carpellary bundles. All other floral vascular traces originate from the inner system.

Filament and corolla growth in flowers of lpomoea nil are inhibited by ethylene production. Anthers inhibited filament growth in vitro during younger stages of development even in the presence of the growth promoter gibberellic acid (GA3). To test whether the anthers could be sources of 1-aminocyclopropane-1-carboxylic acid (ACC) endogenous levels of ACC and ethylene production were monitored using gas chromatography. To also test whether the filaments could be transport vectors for ACC the movement of [14CJACC was assessed by scintillation counting from donor agarose blocks, through filament sections, and into receiver agarose blocks. While ACC levels fluctuated in anthers 87 to 21 h before anthesis, anthers contained increased levels of ACC from 15 to 6 hours before anthesis. Ethylene production also fluctuated but peak levels were shifted about 6 hours closer to anthesis than ACC levels within the anthers. Both ACC and ethylene levels in filaments showed fluctuations similar to those in the anthers.[14C]ACC movement became increasingly basipetal during development. Older stages showed greater polar[14C]ACC efflux rates, while all stages showed constant polar influx rates. Low levels of endogenous ACC were transported basipetally from the anther through the filament into agarose blocks at all stages of development. Corresponding levels of endogenous ethylene production remained constant between the varous stages during ACC transport. We have evidence that stamens of 1. nil have a role as source tissues and transport vectors for ACC, to stimulate corolla growth, such as corolla unfolding and senescence.

No abstract

Filament growth in the morning glory Ipomoea nil is promoted by gibberellic acid (GA3) and inhibited by ethylene production during the earlier stages in development (Koning and Raab, 1987). The effects of anther removal on filament growth were examined in I. nil. Three‐quarters of the calyx and corolla tissues were removed in order to emasculate the stamens. This removal caused filament growth to be inhibited in the intact stamens (69 hr before anthesis) as well as the emasculated stamens (69 to 21 hr before anthesis). When the ethylene biosynthesis inhibitors CoCl2 and aminoethoxyvinylglycine (AVG) were applied in separate experiments (to eliminate wound ethylene generated by the damaged tissues), filament growth was promoted to control levels observed in intact flower buds (69 hr before anthesis). Our data suggest that the wounding effect from the calyx and corolla tissues and subsequent reduction in filament growth override any observable effects with anther removal on filament growth. Apparently, the removal of the calyx and corolla tissues severs a normal hormonal relationship between these floral organs and the developing filament.

No abstract