• Korean Journal of Fisheries and Aquatic Sciences
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• v.16 no.3
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• pp.265-272
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• 1983

Carpogonia, spermatangia and carposporangia are demonstrated for North Atlantic plants of Audouinella alariae (Jonsson) Woelkerling for the first time. The plants are monoecious. Carpogonia are terminal on short branches and give rise to short trichogynes laterally. Spermatangia are usually borne in pairs on the supporting cells of carpogonia. Fertilized carpogonia give rise to 3-4 carposporangia. Morphology of sexual reproductive structures and postfertilization development provide characteristics for distinguishing A. alariae from A. rhipidandra (Rosenvinge) Dixon, which were previously synonymized.

• Journal of Plant Biology
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• v.28 no.1
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• pp.45-55
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• 1985

Observations on reproduction of Rhodochorton purpureum (Lightfoot) Rosenvinge (Acrochaetiaceae, Rhodophyta) was carried out with plants from Hokkaido, Japan. This species produces no monosporangia both in nature and culture, even though it does tetrasporangia commonly. The plants from Nemuro produce neither sporangia nor gametangia, and thus vegetative reproduction is the only known way to propagate themselves. It is suggested that the vegetative reproduction occurs in nature by fragmentation of vegetative filaments after development of a rhizoid. Several different modes of rhizoid production are described. The plants from Akkeshi and Oshoro (I) produce tetrasporangia that develop into plants producing only tetrasporangia. The plants from Muroran and Oshoro (II) produce tetrasporangia that develop into gametophytes. Gametophytes of R. purpureum from Muroran produce tetrasporangia as well as spermatangia or carpogonia. Such tetrasporangia on gametophytes are presumed to be mitotic.

• ALGAE
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• v.21 no.3
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• pp.323-332
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• 2006

Mitochondrial distribution and abundance were assessed during the growth of apical and subapical cells in the red algae Colaconema caespitosum (J. Agardh) Jackelman, Stegenga and Bolton and Antithamnion cruciatum (C. Agardh) Nägeli after staining with 3,3’-dihexyloxacarbocyanine iodide [DiOC6(3)] and 2,4’-dimethylaminostyryl-Nethylpyridinium iodide (DASPEI). In fully elongate apical cells of C. caespitosum there were 100-120 mitochondria. During apical cell enlargement and division there is a doubling and then halving of the mitochondrial numbers. Apical cells prior to cytokinesis in young filaments are smaller than in mature filaments (ca. 50 and 100 μm long, respectively) and have fewer mitochondria (ca. 100 and 120 mitochondria per cell, respectively). In older vegetative cells mitochondria tend to aggregate at opposite ends of the cells with some mitochondria associated with the central nucleus or at points of apparent branch initiation. There is a greater density of mitochondria in apical cells of smaller versus larger plants (one mitochondrion per 6.3 μm3 and 9.8 μm3, respectively), suggesting that apical cells of younger plants may be more metabolically active. Male and female gametophytic thalli of Antithamnion cruciatum had similar numbers of mitochondria in apical cells of indeterminate axes, as did gametophytic and sporophytic thalli. There were about 40-50 mitochondria in fully elongated apical cells with about half this number in newly divided apical and subapical cells. Apical cells of determinate branches had more mitochondria (60-77) than indeterminate branches (60-70 vs. 40-50). In both species and in all cell types mitochondrial numbers were highly correlated with cell size.