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Abstract: The morphology and infraciliature of a new ciliate, Aspidisca hongkongensis spec. nov., a large marine form isolated from the coastal waters near Hong Kong, were investigated. It differs from the congeners by the combination of cell size (about 90×60μm in vivo), 9–11 conspicuous dorsal ridges, one fine and seven strong frontoventral cirri, six membranelles in anterior portion of adoral zone, and 17–23 membranelles in posterior portion of adoral zone. The comparison with similar congeners clearly supports the distinction of this new species based on morphological and small subunit (SSU) rRNA gene sequence studies. The SSU rRNA gene sequence similarity within the genus is about 75.3–92.1% which indicates that this is a distinct form. Phylogenetic trees based on SSU rRNA gene information show that A. hongkongensis groups with A. leptaspis. [Copyright &y& Elsevier]

The morphology and infraciliature of Orthodonella sinica n. sp. and Apokeronopsis wrighti n. sp., isolated from the coastal water off Hong Kong, were investigated in living and stained specimens. Orthodonella sinica n. sp. is diagnosed as: a marine Orthodonella 150–310 × 40–80 μm in vivo; with a dominant beak-like projection at the anterior end; about 70 somatic kineties; 84–126 dikinetids in the synhymenium; one contractile vacuole in the posterior one-fourth of cell, near the left margin; one conspicuous dorsal suture. Apokeronopsis wrighti n. sp. is diagnosed as: an Apokeronopsis about 150–230 × 35–55 μm in vivo; dark-reddish blood-cell-shaped cortical granules grouped in three rows on the ventral side and two rows on the dorsal side; 23–35 cirri in the right mid-ventral rows (MVR) and 23–32 cirri in the left MVR; six to eight buccal, two frontoterminal, 30–42 left marginal, and 32–43 right marginal cirri; 21–30 transverse cirri extending anteriorly beyond the level of mid-body; consistently three dorsal kineties. The separation of A. wrighti n. sp. and its highly similar congeners Apokeronopsis crassa and Apokeronopsis bergeri was supported by comparison of their SSrRNA gene sequences. [ABSTRACT FROM AUTHOR]