A further description of the green dinoflagellate, strain Y‐100, with a chlorophyll a‐ and b‐containing endosymbiont is given with special emphasis on the morphology of the host cell. The host dinoflagellate cell is unarmored and has a gymnodinoid overall appearance. The theca or amphiesma basically consists of the outer membrane and flattened thecal vesicles in which no thecal plates are developed. Unusual hand basket‐shaped scales cover the entire cell surface together with a layer of mucilaginous material. These findings suggest that the organism is a new member of the Gymnodiniaceae (Gymnodiniales). We propose the name Lepidodinium viride gen. et sp. nov. The ultrasturcture of the host cell is typical of the dinoflagellates; however, the organism has 1) an unusual cytoplasmic projection that may be a homologue of the peduncle, 2) a single membrane‐bounded body containing membranous sheets, closely situated next to the endosymbiont, and 3) an electron opaque network‐forming appendage surrounding the transverse flagellum. Name of these features have been found in other dinoflagellates.

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A green‐colored marine unicell has been grown in unialgal culture and its morphology, chloroplast fine structure, and chlorophyll composition investigated. The organism is typical of dinoflagellates in its shape, flagellation, nucleus, mitochondria, and trichocysts. It is similar to Gymnodinium but possesses fine body scales. Chloroplasts and two kinds of vesicles bounded by double membranes, but no organelles obviously identifiable as nuclei or mitochondria, are associated in ribosome‐dense cytoplasm separated by a double membrane from the dinophycean cytoplasm. The chloroplasts are unlike any previously reported for dinoflagellates. Each is enclosed by an envelope consisting of a double membrane. Chloroplast lamellae consist of three appressed thylakoids. Interlamellar pyrenoids are present. Pigment analysis reveals chlorophylls a and b but not chlorophyll c. It seems likely that the organism is an undescribed dinoflagellate containing an endosymbiont with chlorophylls a and b and that the reduction of the endosymbiont nucleus and mitochondria has permitted a more initmate symbiosis.

Cellular and body scale structure of Heterocapsa ovata sp. nov. and Heterocapsa orientalis sp. nov. (Peridiniales, Dinopbyceae) MITSUNORI IWATAKI'*t, LIZETH BOTEs2, TOMOHIRO SAWAGUCHI3, KATSUSHI SEKIGUCHI4 AND YASUWO FUKUyo5

SUMMARY A method for the Cryopreservation of Microcystis aeruginosa f. aeruginosa is described. For the five strains tested, dimethyl sulfoxide (DMSO) (3% v/v) was the only effective cryoprotectant for freezing to, and thawing from ‐196°C and allowed the successful recovery (>50%) of all the strains. The viability of frozen material was independent of the period of storage in liquid nitrogen. The strain NIES‐44 (National Institute for Environmental Studies) had a recovery level of greater than 90% at 3–10% (v/v) DMSO in both two step and rapid cooling methods. The other three strains, NIES‐87, 88 and 89 had greater than 60% of viability after freeze/thawing in presence of both 3% and 5% DMSO concentrations. On the other hand, the strain NIES‐90 showed approximately 50% of viability in only 3% DMSO solution after two step cooling to and thawing from ‐196°C. This strain was damaged by greater than 4% DMSO and by rapid cooling to ‐196°C. It was found that cold shock injury and the cytotoxicity of DMSO were different at a strain level.