Comparative Anatomy of Ovules in Galinsoga, Solidago and Ratibida (Asteraceae)

Many Asteraceae species have been introduced into horticulture as ornamental or interesting exotic plants. Some of them, including Solidago and Galinsoga, are now aggressive weeds; others such as Ratibida are not. Special modifications of the ovule tissue and the occurrence of nutritive tissue have been described in several Asteraceae species, including invasive Taraxacum species. This study examined whether such modifications might also occur in other genera. We found that the three genera examined - Galinsoga (G. quadriradiata), Solidago (S. canadensis, S. rigida, S. gigantea) and Ratibida (R. pinnata) - differed in their nutritive tissue structure. According to changes in the integument, we identified three types of ovules in Asteraceae: “Taraxacum” type (recorded in Taraxacum, Bellis, Solidago, Chondrilla), with well-developed nutritive tissue having very swollen cell walls of spongy structure; “Galinsoga” type (in Galinsoga), in which the nutritive tissue cells have more cyto-plasm and thicker cell walls than the other integument parenchyma cells, and in which the most prominent character of the nutritive tissue cells is well-developed rough ER; and “Ratibida” type (in Ratibida), in which the nutritive tissue is only slightly developed and consists of large highly vacuolated cells. Our study and future investigations of ovule structure may be useful in phylogenetic analyses.

Pullulan elaboration and differentiation of the resting forms in Aureobasidium pullulans

To identify the cellular forms that are responsible for the synthesis of pullulan produced by Aureobasidium pullulans, we performed cytochemical and ultrastructural localizations of glucan in the cellular forms of this microorganism (blastospores and resting forms). Growth conditions, cell populations, and pullulan production were studied concurrently. Our results are consistent with a model in which the resting forms (swollen cells and chlamydospores) might be primarily involved in this extracellular polysaccharide elaboration. At the cellular level, pullulan production could be the result of three main stages: (i) cell wall thickening and extracellular polysaccharide synthesis by the swollen cell, (ii) fibrillar arrangement of this polysaccharide into pullulan along a capsular network around the chlamydospore, and (iii) subcellular hydrolysis separating the capsule from the periplasmic zone and consequently permitting the solubilization of pullulan in the culture medium. A melanization process in the outer layer of the cell wall and the capsule accompanies these patterns.Key words: Aureobasidium pullulans, capsule, cytochemistry, polysaccharide, pullulan, resting forms.