Amphidiniopsis uroensis sp. nov. and Amphidiniopsis pectinaria sp. nov. (Dinophyceae): Two new benthic dinoflage llates from Japan

Two new armoured, heterotrophic sand‐dwelling marine dinoflagellates, Amphidiniopsis uroensis Toriumi, Yoshimatsu et Dodge sp. nov. and Amphidiniopsis pectinaria Toriumi, Yoshimatsu et Dodge sp. nov. were collected from Japanese sandy beaches, and their morphological features observed by light microscopy and scanning electron microscopy (SEM). The cell size of A. uroensis is 28–31 μm in length and 23–28 μm in width. The plate formula is Po 3′, 3a, 6″, 3c, 4s (+1 acc.), 5″′, 2″″. The thecal surface is ornamented with small processes, pores and spines, however, the surface of plate 2a is smooth. The epitheca possesses a narrow ridge that is extended along on the suture between 1′ and 3′. Plate 1″ connects with the right sulcal (Sd) and right sulcal accessory (Sda) plates, so the cingulum is incomplete. A nucleus is situated in the central part of the cell. There are a few small spines at the antapex. There are no stigma or chloroplasts. Amphidiniopsis pectinaria cells are 33–40 urn in length and 29–35 μm in width. The plate formula is Po 4′, 3a, 7″, 3c, 4s (+1 acc.), 5″′, 2″″. Plate 1″ connects directly with Sd and Sda plates, so the cingulum is incomplete. The thecal surface is ornamented with small processes, spines and pores. The epitheca is provided with a narrow ridge that is extended along on the suture between plates 1′, 4′ and 7″. The ornamentation on the antapical plates is unique. It is arranged in 10 straight rows on the hypotheca; each row has a strong spine at its posterior end. In addition, there is a long spine at the antapex. There are no stigma or chloroplasts. A nucleus is located in the central part of the cell.     

Light and scanning microscopy of two benthic species of Amphidiniopsis (Dinophyceae), Amphidiniopsis hexagona sp. nov. and Amphidiniopsis swedmarkii from Japan

Two species of the genus Amphidiniopsis, a marine armoured, sand‐dwelling dinoflagellate, Amphidiniopsis hexagona Yoshimatsu, Toriumi et Dodge sp. nov. and Amphidiniopsis swedmarkii (Balech) Dodge were collected from Japanese sandy beaches, and their morphologic features were observed by light microscopy and scanning electron microscopy. Amphidiniopsis hexagona was hexagonal in ventral view and measured 44–59 urn in length and 40–53 urn in width. The plate formula is P_o, 4′, 2a, 7″, 3c, 4s (+ 2 accessory), 5″″, 2″″. This plate arrangement of A. hexagona is essentially the same as those of Amphidiniopsis hirusta and A. swedmarkii, but this new species can be readily distinguished from the latter two species by the following characters: (i) the cell shape; (ii) the presence of an antapical spine; and (iii) the surface ornamentation of thecal plates.     

Morphology of Sinophysis minima sp. nov. and three Sinophysis species (Dinophyceae, Dinophysiales) from the Sea of Japan

Four sand‐dwelling species of the marine dinoflagellate genus Sinophysis, including one new species, have been examined from intertidal and subtidal sand, from the Sea of Japan. The morphological features of these species were observed by light and scanning electron microscopy. Sinophysis minima sp. nov. is flattened laterally and is 17.5–35.0 μm in length and 15.0–27.5 μm in depth, with a length/depth ratio of 1.1–1.4, an epitheca depth of 5.0–7.5 μm, and a sulcus length of about three‐quarters the hypotheca length. Sinophysis ebriola (Herdman) Balech, Sinophysis grandis Hoppenrath and Sinophysis stenosoma Hoppenrath were recorded for the first time in the seas of Russia. Sinophysis stenosoma is the most common species in the Sea of Japan. All species usually occurred together in the region investigated. Additional information on the known species is provided.     

Roscoffia minor sp. nov. (Peridiniales, Dinophyceae): A new, sand-dwelling, armored dinoflagellate from Hokkaido, Japan

A new, sand-dwelling, armored dinoflagellate, Roscoffia minor sp. nov., is described from Ishikari beach, Hokkaido, Japan. The dinoflagellate has been collected from sand samples taken both near the water's edge and further upshore (25 m from the water's edge at a depth of 1 m), indicating that it is a true sand-dwelling species. Roscoffia minor is heterotrophic and lacks both a chloroplast and an eye-spot. The cell consists of a flattened cap-shaped epitheca and a large hemispheroidal hypotheca, and it is quite different from cells of the typical armored dinoflagellates. The thecal plate formula is: Po, 3′, la, 5″, 3c, 3s, 5″, 1″″. Its distinct cell shape and the thecal plate arrangement indicate affinity to the monotypic genus Roscoffia. Roscoffia minor is distinguished from Roscoffia capitata, the type species, by its smaller size and the possession of a finger-like apical projection. The thecal arrangement of the epitheca is similar to those of the members of the family Podolampaceae, while the hypothecal arrangement is the same as that of members of the subfamily Diplopsalioideae (family Congruentidiaceae). The organism seems to be positioned somewhere intermediate between these two families, but the family to which this dinoflagellate should be affiliated could not be determined.     

Taxonomy of some common Amphidinium species

The taxonomic status of several well known species belonging to the genus Amphidinium (Dinophyceae) has been re-examined. Studies in culture and observations on the micro-anatomy of these organisms suggest that the number of species can be reduced to two, A. klebsii and A. carterae. They may be distinguished on the basis of fundamental differences in chloroplast morphology.     

PROROCENTRUM BELIZEANUM,PROROCENTRUM ELEGANS,AND PROROCENTRUM CARIBBAEUM,THREE NEW BENTHIC SPECIES (DINOPHYCEAE) FROM A MANGROVE ISLAND,TWIN CAYS,BELIZE1

Three new benthic dinoflagellate species, Prorocentrum belizeanum, Prorocentrum elegans, and Prorocentrum caribbaeum, from mangrove floating detritus are described from scanning electron micrographs. Species were identified based on shape, size, surface micromorphology, ornamentation of thecal plates, and architecture of the periflagellar area and intercalary band. Cells of P. belizeanum are round to slightly oval with a cell size of 55–60 μm long and 50–55 μm wide. Areolae are round and numerous (853–1024 per valve) and range from 0.66 to 0.83 μm in size. The periflagellar area of P. belizeanum is a broad V-shaped depression; it accommodates a flagellar and an auxiliary pore and a flared, curved apical collar. The intercalary band of P. belizeanum is horizontally striated. Prorocentrum elegans is a small species 15–20 μm long and 10–14 μm wide, with an ovate cell shape. The thecal surface is smooth. Two sizes of valve pores were recognized: large, round pores (20–22 per valve) arranged in a distinct pattern and smaller pores situated in an array along the intercalary band. The periflagellar area is V-shaped; it accommodates an uneven sized flagellar pore, an auxiliary pore, and an angled protuberant flagellar plate. The intercalary band is transversely striated. It is a bloom-forming species. Prorocentrum caribbaeum cells are heart-shaped with a rounded anterior end and a pointed posterior end. Cells range from 40 to 45 μm long and 30 to 35 μm wide. Thecal surface has two different-sized pores: large, round pores (145–203 per valve) arranged perpendicularly from the posterior margins, and small, round pores unevenly distributed on the thecal surface. The periflagellar area is ornate. It is V-shaped with a curved apical collar located next to the auxiliary pore; a smaller protuberant apical plate is adjacent to the flagellar pore. The intercalary band is transversely striated and sinuous. Cells are active swimmers.     

In situ and experimental evidence of the influence of turbulence on cell division processes of Peridinium cinctum forma westii (Lemm.) Lefèvre

Comparison of the diel variations of the wind intensity and the division rate (DR) of Peridinium cinctum forma westii (Lemm.) Lefèvre in situ reveals that the intensity of the wind blowing throughout the whole day does not affect the DR. On the other hand, a strong inhibitory effect is noticed when the wind episodes occur during the time period 18.00–02.00 h. Systematic hourly sampling and staining of Peridinium cells showed that nuclear division takes place between 23.00 and 02.00 h and is completed before cytokinesis begins. Thus the time period 18.00–02.00 h corresponds to the premitotic and mitotic phases of cell division, and the turbulence generated by the wind affects the process of nuclear division.

The relationship between water turbulence and the DR of Peridinium which was observed in Lake Kinneret (Israel) has been checked under experimental conditions. Peridinium was grown without shaking, with continuous rotary shaking and with intermittent shaking at 100 r min^-1. The specific growth rate (k), generation time (G) and mortality rate were followed and compared. The results obtained confirm the facts observed in situ and clarify some aspects. Intermittent shaking of 2 h day^-1 during the dark phase reveals the inhibitory effect of agitation on nuclear division. Continuous shaking causes a high rate of cell mortality. Shaking during the light period does not affect the division process.

The effect of turbulence on the DR of Peridinium explains why the timing of the bloom in Lake Kinneret is a function of the duration and intensity of the mixing period in the lake.     

ULTRASTRUCTURE OF A NEW SAND-DWELLING DINOFLAGELLATE,SCRIPPSIELLA ARENICOLA SP. NOV1

A new dinoflagellate, Scrippsiella arenicola Horiguchi et Pienaar sp. nov., is described from tidal pools with sandy substrates along the east coast of South Africa. S. arenicola exhibits a vertical migratory rhythm which is in synchrony with the tidal cycle. It is a medium-sized armoured dinoflagellate with many rod-shaped chloroplasts. Thecal plate arrangement is pp, x, 4′, 3a, 7′, 6c, 5′, 2″ and 4s. The 2a and 3a plates are separated from each other. S. arenicola has several unique ultrastructural features. Electron-dense fibres are found on the protruded part of the thecal plates, such as on the ornamental projections or extremities of the lists. In addition to the 9 + 2 axoneme, additional fibres are found in the free moving part of the longitudinal flagellum. The portion of the transverse flagellum covered by the left sulcal list possesses a dense array of mastigonemes which connect the flagellum and the cell. The flagellar pore platelets differ from ordinary thecal plates in their thickness and fibrous nature. The ultrastructure of the apical stalk and its associated structures is described. The vertical migration and mode of cell division is also described.