Taxodiaceae

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  • seed cone and ovule ontogeny in metasequoia sequoia and sequoiadendron Taxodiaceae coniferales
    Botanical Journal of the Linnean Society, 1992
    Co-Authors: T. Takaso, P B Tomlinson
    Abstract:

    TAKASO, T. & TOMUNSON, P. B., 1992. Seed cone and ovule ontogeny in Metasequoia, Sequoia and Sequoiadendron (Taxodiaceae–Coniferales). Structural features of seed cones, up to the initiation of ovules, are developed in the three genera in the summer and late fall prior to pollination in the following spring, when cones renew their further development. Bracts are initiated in a decussate manner in Metasequoia but spirally in Sequoia and Sequoiadendron. No ovuliferous scale is initiated, at most there is a shallow mound of tissue on the adaxial surface of the bract from which the ovules are developed. Metasequoia produces a single series of up to eight ovules in acropetal (centripetal order), Sequoia and Sequoiadendron produce a double series of six to nine ovules, also in acropetal order, since a second series of ovules appear distal to and alternate with the first series. Common features that unite the genera are the somewhat peltate configuration of the cone scales due to late intercalary expansion, the derivation of the vascular supply to the bract-ovule complex from a single bundle and the usual inversion of the seed during late development, to which can be added developmental features. The absence of tooth-like structures, present in some other Taxodiaceae, is discussed in relation to cone evolution in the family being determined by changes in developmental timing. Emphasis is made on the way in which features of morphogenesis, determine cone organization in the three genera independent of an interpretation that relies solely on hypothetical ancestral forms.

  • Seed cone and ovule ontogeny in Metasequoia, Sequoia and Sequoiadendron (Taxodiaceae–Coniferales)
    Botanical Journal of the Linnean Society, 1992
    Co-Authors: T. Takaso, P B Tomlinson
    Abstract:

    TAKASO, T. & TOMUNSON, P. B., 1992. Seed cone and ovule ontogeny in Metasequoia, Sequoia and Sequoiadendron (Taxodiaceae–Coniferales). Structural features of seed cones, up to the initiation of ovules, are developed in the three genera in the summer and late fall prior to pollination in the following spring, when cones renew their further development. Bracts are initiated in a decussate manner in Metasequoia but spirally in Sequoia and Sequoiadendron. No ovuliferous scale is initiated, at most there is a shallow mound of tissue on the adaxial surface of the bract from which the ovules are developed. Metasequoia produces a single series of up to eight ovules in acropetal (centripetal order), Sequoia and Sequoiadendron produce a double series of six to nine ovules, also in acropetal order, since a second series of ovules appear distal to and alternate with the first series. Common features that unite the genera are the somewhat peltate configuration of the cone scales due to late intercalary expansion, the derivation of the vascular supply to the bract-ovule complex from a single bundle and the usual inversion of the seed during late development, to which can be added developmental features. The absence of tooth-like structures, present in some other Taxodiaceae, is discussed in relation to cone evolution in the family being determined by changes in developmental timing. Emphasis is made on the way in which features of morphogenesis, determine cone organization in the three genera independent of an interpretation that relies solely on hypothetical ancestral forms.

  • CONE AND OVULE DEVELOPMENT IN SCIADOPITYS (Taxodiaceae‐CONIFERALES)
    American Journal of Botany, 1991
    Co-Authors: Tokushiro Takaso, P B Tomlinson
    Abstract:

    Ontogeny of seed cones of Sciadopitys, with special reference to the ovule-supporting structure, is studied in material collected in Japan and Massachusetts. Cones are initiated as lateral or terminal structures in summer and complete the formation of most organs before winter. Bract development is well advanced before ovule-supporting structures are initiated. Continued cone development involves the formation of a narrow ridge of tissue in the axil of each fertile bract. This ridge develops a series of nine (but up to 12) apical lobes in centrifugal order, each of which is the primordium of a future tooth on the ovuliferous scale. Ovules are initiated as outgrowths of the adaxial surface of each lobe so that there is a one-to-one ratio between lobes and ovules. Intercalary extension of the ovuliferous scale itself (distally) and the common base of the bract and ovuliferous scale (proximally) greatly extends the complex. The ovuliferous scale eventually exceeds the subtending bract and its apex becomes recurved. Bracts each have a single trace, but each ovuliferous scale has a pair of traces that proliferate distally to irrigate ovule and scale lobe. Intercalary growth results in recurvature of the ovule trace. The organization of the cone is directly comparable with certain Permian fossils. Sciadopitys also seems unique within the Taxodiaceae in its centrifugal development of the ovule-supporting complex.

  • cone and ovule development in sciadopitys Taxodiaceae coniferales
    American Journal of Botany, 1991
    Co-Authors: Tokushiro Takaso, P B Tomlinson
    Abstract:

    Ontogeny of seed cones of Sciadopitys, with special reference to the ovule-supporting structure, is studied in material collected in Japan and Massachusetts. Cones are initiated as lateral or terminal structures in summer and complete the formation of most organs before winter. Bract development is well advanced before ovule-supporting structures are initiated. Continued cone development involves the formation of a narrow ridge of tissue in the axil of each fertile bract. This ridge develops a series of nine (but up to 12) apical lobes in centrifugal order, each of which is the primordium of a future tooth on the ovuliferous scale. Ovules are initiated as outgrowths of the adaxial surface of each lobe so that there is a one-to-one ratio between lobes and ovules. Intercalary extension of the ovuliferous scale itself (distally) and the common base of the bract and ovuliferous scale (proximally) greatly extends the complex. The ovuliferous scale eventually exceeds the subtending bract and its apex becomes recurved. Bracts each have a single trace, but each ovuliferous scale has a pair of traces that proliferate distally to irrigate ovule and scale lobe. Intercalary growth results in recurvature of the ovule trace. The organization of the cone is directly comparable with certain Permian fossils. Sciadopitys also seems unique within the Taxodiaceae in its centrifugal development of the ovule-supporting complex.

Makoto Nishida - One of the best experts on this subject based on the ideXlab platform.

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  • Study of male sterility in Taiwania cryptomerioides Hayata (Taxodiaceae).
    Protoplasma, 2006
    Co-Authors: S.-h. Chen, N-j Chung, Y.-n. Wang, P-f Tsai
    Abstract:

    A study of male sterility over a period of three consecutive years on a conifer species endemic to Taiwan, Taiwania cryptomerioides Hayata (Taxodiaceae), was done for this article. With the aids of fluorescence and electron microscopic observations, the ontogenic processes in the fertile and sterile microsporangia are compared, using samples collected from Chitou Experimental Forest and Yeou-Shoei-Keng Clonal Orchard of the National Taiwan University, Nantou, Taiwan. The development of male strobili occurred from August to the end of March. Microsporogenesis starts with the formation of the archesporium and ends with the maturation of 2-celled pollen grains within the dehiscing microsporangium. Before meiosis, there was no significant difference in ultrastructure between the fertile and sterile microsporangia. Asynchronous pollen development with various tetrad forms may occur in the same microsporangium of either fertile or sterile strobili. However, a callose wall was observable in the fertile dyad and tetrad, but not in the sterile one. After dissolution of the callose wall, the fertile microspores were released into the locule, while some sterile microspores still retained as tetrads or dyads with intertwining of exine walls in the proximal faces. As a result, there was no well developed lamellated endexine and no granulate ectexine or intine in the sterile microspores. Eventually, the intracellular structures in sterile microspores were dramatically collapsed before anthesis. The present study shows that the abortion in pollen development is possibly attributed to the absence of the callose wall. The importance of this structure to the male sterility of T. cryptomerioides is discussed.