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Fallacia is distinguished morpho‐anatomically from Navicula sensu lato based on the possession of an H‐shaped chloroplast, lateral sterna and a finely porous conopeum, but whether this genus is monophyletic is still in question. Three new Fallacia species are described based on morphology and SSU rRNA and rbcL gene sequences: Fallacia tateyamensis sp. nov., Fallacia bosoensis sp. nov. and Fallacia laevis sp. nov. We performed the first comprehensive molecular and morphological phylogenetic analyses of 31 Fallacia species based on 11 new sequences from six species and 23 morphological characters. We also documented the detailed morphogenesis of Fallacia for the first time. Fallacia is not monophyletic. Both morphological and DNA sequence data supported the separation of Rossia from Fallacia, while the phylogenetic position of Pseudofallacia is uncertain. We recognized four morphogroups in Fallacia by morphological and molecular phylogenetic analyses. Ancestral character reconstruction indicated that diatoms in Sellaphoraceae evolved from the possession of two lateral narrow parallel depressions covered by narrow nonporous conopea, to lyre‐shaped canals covered by wide porous conopea. Lanceolate canals and the presence of areolae in canals evolved multiple times independently. [ABSTRACT FROM AUTHOR]

The present study clarifies the fine structure of the vegetative frustules, initial valves and perizonium of Achnanthes crenulata Grunow. The valves of the vegetative cell are distinctly linear-lanceolate with an undulate margin. The valve face is quite flat and in girdle view is smoothly curved as in species of Gephyria (Bacillariophyceae). However, the valve face of the initial cells is slightly rounded and does not have an undulate margin. Furthermore, the rapheless sternum is centrally positioned along the apical axis of the araphid initial valve. As this taxon develops from auxospore to initial valve, it forms only longitudinal perizonial bands; no transverse bands arise. The perizonium consists of three silicified bands: one large, central longitudinal plate and two bands that underlie this plate; these two bands are either open or closed. This taxon has several conspicuous structures compared to other marine species of Achnanthes, but the structure of the perizonium supports the position of A. crenulata within Achnanthes sensu stricto. [ABSTRACT FROM AUTHOR]

SUMMARY The pattern centre in valve morphogenesis is an annulus in centric diatoms or a sternum in pennate diatoms. The genus Rhaphoneis is currently placed within a lineage that diverges at the root of the pennate diatom clade in most molecular phylogenies, and its valves have a unique pattern to their striae, i.e. radiating from both apices, giving the impression that a pattern centre exists at both ends of the valve and virgae (ribs) formation proceeds centripetally. The present study, however, shows that the pattern centre is actually a linear sternum and the formation of virgae proceeds centrifugally, a pattern centre that is commonly found in most araphid diatoms. Thus, the hypothesis that valve morphogenesis based on a linear sternum and perpendicular virgae is a synapomorphy of pennate diatoms is supported. Our study also demonstrates that the pattern of valve formation can be observed by light microscopy with a direct mounting method when the specimen is relatively large, i.e. exceeding approximately 50 µm in valve length. An important advantage of the use of the direct mounting method is that it requires no repeated centrifugation steps for dehydration, steps necessary for observation by a scanning electron microscope, causing the loss and/or collapse of the specimen, particularly with fragile valves in the early stages of development. [ABSTRACT FROM AUTHOR]

Examination of Grammatophora marina from rough and clonal cultures showed that cell size changes were more flexible than is generally reported for diatoms. Allogamous sexual auxosporulation took place through copulation between small male cells and larger female cells, but only in mixed rough culture and never in clonal cultures. Auxospores were also formed without copulation in clonal cultures ('uniparental auxosporulation') and these, like sexual auxospores, developed through formation of a perizonium, which consisted of a series of transverse bands. All of these bands, including the primary band, were open. Circular scales were present in the auxospore wall before initiation of perizonium formation and irregular, elongate structures lined the suture of the transverse perizonium. Perizonium and scales resembled those of another araphid pennate diatom, Gephyria media. Initial cells were formed within the perizonium and consisted of an initial epivalve with a simplified structure, an initial hypovalve (formed beneath the perizonium suture) and a third, normally structured valve formed beneath the epivalve; the epivalve was then sloughed off. Initial cells of similar configuration but often aberrant morphology could also be formed through expansion from vegetative cells, without involvement of a perizonium. Vegetative cells were also capable of limited enlargement through simple expansion without formation of an initial cell, and abrupt size reduction. Cell size ranges in populations from different regions suggest that G. marina may contain pseudocryptic species. [ABSTRACT FROM AUTHOR]

Grazing effects of ayu, Plecoglossus altivelis Temminck et Schegel, on the benthic algal assemblages were investigated in the Chikuma River, Japan. Comparison of the algal composition on boulders with and without intensively grazed patches indicated that fish grazing decreased the abundance of diatoms and prostrate filamentous cyanobacteria and caused upright filamentous cyanobacteria to predominate. Differential consumption by ayu was estimated by comparing the relative abundance of algae in the stomach contents of ayu and that in the algal assemblages within the grazed patches. The results showed that ayu consumed the prostrate filamentous cyanobacteria proportionally to their abundance, whereas they ingested diatoms and the upright filamentous cyanobacteria in a larger and lower quantity, respectively, than that expected from their abundance. Differential consumption would involve the change in the algal composition toward the predominance of upright filamentous cyanobacteria under fish grazing conditions. [ABSTRACT FROM AUTHOR]

This study clarifies the fine structure of the vegetative and initial valves of Achnanthes yaquinensis and briefly compares them to other Achnanthes species. It also elucidates the structure of the perizonium, based on auxospore development in short-term cultures. The araphid valve has marginal ridges and terminal spines that allow connecting valves to form a chain. The terminal spines develop from the rapheless sternum. The complete cingulum consists of 3–5 split bands with two rows of areolae. These features can be used to discriminate species within the genus. Sexual reproduction is isogamous with two mother cells producing two auxospores, which are enclosed in mucilage. The perizonium develops on one side of an auxospore only, comprising one large central longitudinal band and four closed bands. There are no transverse perizonial bands. The raphid valve of the initial cell forms first, underneath the longitudinal perizonium, followed by the araphid valve, which is not covered by any perizonial bands. The araphid valve of the initial cells lacks a marginal spine, and the rapheless sternum lies more centrally than in the vegetative cell. The relationship of the genus Achnanthes to other monoraphid diatoms is discussed briefly. [ABSTRACT FROM AUTHOR]

SUMMARYThe morphology and fine valve structure of the marine epiphytic diatom Cocconeis heteroidea Hantzsch have been investigated. The entire frustule, including the internal and external structure of the raphid valve (RV) and araphid valve (AV), and the complete cingulum, are described using light microscopy and scanning and transmission electron microscopy, using a bleaching method. The strongly sigmoid raphe terminates in elongate hooked helictoglossae internally. The hymenes, with perforations arranged in a centric array, are located near the internal openings of the areolae in the RV. The striae in the AV consist of alveoli occluded by hymenes, that have perforations arranged in a parallel array and are located near the outer surface. The complete cingulum of AV consists of three open bands without fimbriae: a valvocopula, a copula with a ligula and a pleura with a small ligula. The RV has only a valvocopula which is open type and not fimbriate. [ABSTRACT FROM AUTHOR]

SUMMARYA new species of Cocconeis has been found growing on the green seaweed Caulerpa racemosa (Forsskål) J. Agardh var. laete-virens (Montagne) Weber van Bosse from Shikine Island in the Izu Islands on the Pacific coast of Japan; we propose the name Cocconeis shikinensis Hid. Suzuki and describe the species by light microscopy (LM) and electron microscopy (EM). This taxon was also collected from the plastic plates used for rearing in seed production systems of the abalone Nordotis discus hannai Ino and the horned turban Turbo cornutus Solander in the Toyama Prefectural Fisheries Research Institute facing the Sea of Japan. The main morphological features of C. shikinensis are as follows. The valves are elliptic. The valve face of the raphid valve (RV) is slightly concave and that of the araphid valve (AV) is complementary to the RV and convex. The single plastid is flat, C-shaped and elaborately lobed. The raphe on the RV is straight. The each terminal area expands to both sides along the valve margin, forming an arrowhead-shaped, thickened hyaline area. The striae consist of small, round areolae and are radiate and uniseriate. On the AV, the striae consist of several alveoli. Each alveolus opens internally by means of a circular foramen. The valvocopula of each valve is fimbriate and open. The cingulum attached to the AV consists of three girdle bands; a valvocopula and two bands (copula and pleura), which are open and have ligulae. The relationship between C. shikinensis and similar members of the genus Cocconeis is discussed. [ABSTRACT FROM AUTHOR]