The genus Taraxacum Wigg. (Asteraceae) forms a polyploid complex within which there are strong links between the ploidy level and the mode of reproduction. Diploids are obligate sexual, whereas polyploids are usually apomictic. The paper reports on a comparative study of the ovary and especially the ovule anatomy in the diploid dandelion T. linearisquameum and the triploid T. gentile. Observations with light and electron microscopy revealed no essential differences in the anatomy of both the ovary and ovule in the examined species. Dandelion ovules are anatropous, unitegmic and tenuinucellate. In both sexual and apomictic species, a zonal differentiation of the integument is characteristic of the ovule. In the integumentary layers situated next to the endothelium, the cell walls are extremely thick and PAS positive. Data obtained from TEM indicate that these special walls have an open spongy structure and their cytoplasm shows evidence of gradual degeneration. Increased deposition of wall material in the integumentary cells surrounding the endothelium takes place especially around the chalazal pole of the embryo sac as well as around the central cell. In contrast, the integumentary cells surrounding the micropylar region have thin walls and exhibit a high metabolic activity. The role of the thick-walled integumentary layers in the dandelion ovule is discussed. We also consider whether this may be a feature of taxonomic importance.

Although callose occurs during megasporogenesis in most flowering plants, the knowledge about its general function and the mechanisms by which the callose layer is formed in particular places is still not sufficient. The results of previous studies suggest a total lack of callose in the ovules of diplosporous plants in which meiosis is omitted or disturbed. This report is the first documentation of callose events in dandelions ovules. We demonstrated the pattern of callose deposition during the formation of megaspores through diplospory of Taraxacum type and during normal meiotic megasporogenesis in apomictic triploid Taraxacum atricapillum and amphimictic diploid Taraxacum linearisquameum. We found the presence of callose in the megasporocyte wall of both diplosporous and sexual dandelions. However, in a diplosporous dandelion, callose predominated at the micropylar pole of megaspore mother cell (MMC) which may be correlated with abnormal asynaptic meiosis and may indicate diplospory of the Taraxacum type. After meiotic division, callose is mainly deposited in the walls between megaspores in tetrads and in diplodyads. In subsequent stages, callose gradually disappears around the chalazal functional megaspore. However, some variations in the pattern of callose deposition within tetrad may reflect variable positioning of the functional megaspore (FM) observed in the ovules of T. linearisquameum.

Total absence of callose in the ovules of diplosporous species has been previously suggested. This paper is the first description of callose events in the ovules of Chondrilla juncea, which exhibits meiotic diplospory of the Taraxacum type. We found the presence of callose in the megasporocyte wall and stated that the pattern of callose deposition is dynamically changing during megasporogenesis. At the premeiotic stage, no callose was observed in the ovules. Callose appeared at the micropylar pole of the cell entering prophase of the first meioticdivision restitution but did not surround the megasporocyte. After the formation of a restitution nucleus, a conspicuous callose micropylar cap and dispersed deposits of callose were detected in the megasporocyte wall. During the formation of a diplodyad, the micropylar callose cap decreased and the walls of a newly formed megaspores showed scattered distribution of callose. Within the older diplodyad, callose was mainly accumulated in the wall between megaspores, as well as in the wall of the micropylar cell; however, a dotted fluorescence of callose was also visible in the wall of the chalazal megaspore. Gradual degradation of callose in the wall of the chalazal cell and intense callose accumulation in the wall of the micropylar cell were related to the selection of the functional megaspore. Thus, our findings may suggest that callose fulfills a similar role both during megasporogenesis in sexual angiosperms and in the course of meiotic diplospory in apomicts and seems to form a regulatory interface between reproductive and somatic cells.

This study represents the first report on the embryological characteristics of triploid male-sterile dandelion Taraxacum belorussicum (section Palustria) from Poland. While this taxon is considered to be a male-sterile species, we found that the investigated individuals produced pollen. Irregular tetrads, triads and diads with microspores of unequal size were observed in the pollen loculi as a result of disturbed meiotic division, while anthers’ tapetum did not show structural disorders. Possible reasons for the plasticity in the expression of male sterility, as well as the role of pollen in apomicts, are discussed. Flowers of the examined individuals contained well-developed nectaries. The course of embryological processes in the ovules indicated an apomictic mode of reproduction in T. belorussicum. We observed meiotic diplospory of the Taraxacum type, in which first meiotic division starts but results in nuclear restitution, while undisturbed second meiotic division gives rise to a dyad of unreduced megaspores (diplodyad). After three mitotic divisions of the chalazal megaspore, a seven-celled unreduced female gametophyte developed. The features of ovule anatomy and characteristics of a mature female gametophyte corresponded to these described in sexually reproducing dandelions.

An essential, but still not fully understood, aspect of angiosperms’ reproduction is the issue of callose deposition during early female reproductive processes in sexual and apomictic taxa. It was believed that callose may be a marker for an early identification of the reproduction mode and lack of callose was suggested as characteristic for apomicts. However, our findings clearly prove that meiotic diplospory of the Taraxacum type is accompanied by callose deposition and show that lack of callose is not an obligatory feature of the apomictic reproduction mode. In young ovules of C. brevirostris, callose was a marker of the cell entering the first meiotic division restitution. Synthesis and degradation of callose followed a strictly defined pattern, which differed from that described in the majority of analyzed angiosperms. Callose deposition began at the micropylar pole of the diplosporous megaspore mother cell and, finally, this cell wall polysaccharide showed a bipolar location. This pattern dynamically changed in the later stages of meiotic diplospory and, like in sexual species, it was related to the selection of the functional megaspore. Thus, it seems that callose can play a similar regulatory function in cell-cell communication between somatic tissues and the reproductive precursor cell in the ovules of both sexual and diplosporous taxa.