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Abstrakt

Megasporogenesis and female gametophyte development were investigated in ovules of the everbearing strawberry Fragaria x ananassa Duch. cv. Selva. Observations of thin sections revealed that ovule development starts from the formation of a nucellus and coincides in time with the beginning of receptacle overgrowth. The most characteristic feature during nucellus differentiation is the formation of a multicellular archesporium, beginning from at least two cells. Analysis of female gametophyte development indicated that in addition to the meiotic mode, female gametophytes develop by an apomeiotic mode of Antennaria type. Asynchronous development of female gametophytes of different origin occurs. The mature, eight-nucleate, seven-celled female gametophyte of meiotic origin is cylindrical and slightly curved. It occupies the central part of the nucellus. The egg apparatus, consisting of an egg cell and two synergids, is formed in the micropylar part of the female gametophyte; the opposite chalazal pole is occupied by antipodal cells. Besides the ovule in which only one seven-celled female gametophyte finally develops, ovules with a different number of cells were observed to initiate female gametophyte development. Some ovules contain a nucellus with a tetrad of linearly arranged megaspores surrounded by enlarged cells, each of which has the potential to develop into an apomictic female gametophyte. After degeneration of some post-meiotic cells or developmentally advanced female gametophytes, some of the chalazal cells initiated female gametophyte development.
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Abstrakt

Abstract Using monoclonal antibodies (mAbs) JIM13, JIM15 and MAC207, we investigated the temporal and spatial dis-tribution of some arabinogalactan protein (AGP) epitopes in cells of the Bellis perennis L. anther at different developmental stages. AGP epitopes recognized by JIM13 were detected in the protoplasts of tapetal cells, dividing microsporocytes, and microspores; AGP epitopes recognized by JIM15 were present in the cytoplasm of tapetal cells only at the stage with tetrads of microspores in the anther loculus. AGP epitopes recognized by MAC207 were present in the cells of different somatic tissues of the flower bud, but after asymmetric mitosis in the microspore they appeared abundantly in the protoplasts of immature pollen and were still present in mature pollen grains. Callose, revealed by mAb, appeared at the same stage of microsporocyte division as AGPs labelled with JIM13 and JIM15. We discuss the differences in callose and AGP localization and the possible role of the latter during anther development.
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Abstrakt

Our macroscopic observations and microscopic studies conducted by means of a light microscope (LM) and transmission electron microscope (TEM) concerning the reproduction biology of Colobanthus quitensis (Caryophyllaceae) growing in natural conditions in the Antarctic and in a greenhouse in Olsztyn (northern Poland) showed that this plant develops two types of bisexual flowers: opening, chasmogamous flowers and closed, cleistogamous ones. Cleistogamy was caused by a low temperature, high air humidity and strong wind. A small number of microspores differentiated in the microsporangia of C. quitensis , which is typical of cleistogamous species. Microsporocytes, and later micro − spores, formed very thick callose walls. More than twenty spheroidal, polypantoporate pollen grains differentiated in the microsporangium. They germinated on the surface of receptive cells on the dry stigma of the gynoecium or inside the microsporangium. A monosporic embryo sac of the Polygonum type differentiated in the crassinucellar ovule. During this differentiation the nucellus tissue formed and stored reserve materials. In the development of generative cells, a male germ unit (MGU) with differentiated sperm cells was observed. The smaller cell contained mainly mitochondria, and the bigger one plastids. In the process of fertilization in C. quitensis only one nucleus of the sperm cell, without cytoplasm fragments, entered the egg cell, and the proembryo developed according to the Caryophyllad type. Almost all C. quitensis ovules developed and formed perispermic seeds with a completely differentiated embryo both under natural conditions in the Antarctic and in a greenhouse in Olsztyn.
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Abstrakt

The development of megasporocytes and the functional megaspore formation in Deschampsia antarctica were analyzed with the use of microscopic methods. A single archesporial cell was formed directly under the epidermis in the micropylar region of the ovule without producing a parietal cell. In successive stages of development, the meiocyte was transformed into a megaspore tetrad after meiosis. Most megaspores were arranged in a linear fashion, but some tetrads were T-shaped. Only one of the 60 analyzed ovules contained a cell in the direct proximity of the megasporocyte, which could be an aposporous initial. Most of the evaluated D. antarctica ovules featured monosporic embryo sacs of the Polygonum type. Approximately 30% of ovules contained numerous megaspores that were enlarged. The megaspores were located at chalazal and micropylar poles, and some ovules featured two megaspores - terminal and medial - in the chalazal region, or even three megaspores at the chalazal pole. In those cases, the micropylar megaspore was significantly smaller than the remaining megaspores, and it did not have the characteristic features of functional megaspores. Meiocytes and megaspores of D. antarctica contained polysaccharides that were detectable by PAS-reaction and aniline blue staining. Starch granules and cell walls of megasporocytes, megaspores and nucellar cells were PAS-positive. Fluorescent callose deposits were identified in the micropylar end of the megasporocytes. During meiosis and after its completion, thick callose deposits were also visible in the periclinal walls and in a small amount in the anticlinal walls of megaspores forming linear and T-shaped tetrads. Callose deposits fluorescence was not observed in the walls of the nucellar cells.
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