Liqiong Li

The urostylid family Pseudokeronopsidae Borror and Wicklow, 1983 was considered to be a well-outlined taxon. Nevertheless, recent evidence, including morphological, ontogenetic, and molecular information, has consistently revealed the polyphyly of this family. In the present work, a new population of Thigmokeronopsis stoecki Shao et al., 2008 was found and its binary divisional process was described for the first time. In addition, the morphogenetic features of Thigmokeronopsis species and all the other pseudokeronopsids, for which detailed ontogenetic data are available, were rechecked and compared. This reveals that: (1) the ontogenetic process of T. stoecki corresponds well with its congeners T. jahodai and T. rubra except for the macronuclear behavior; (2) Apokeronopsis and Thigmokeronopsis share a similar ontogenetic mode despite of the differences in the number and origin of their buccal cirri; (3) most pseudokeronopsids share the same pattern in the origins of their oral primordia and fronto-ventral-transverse cirral anlagen, except for Pseudokeronopsis similis, which may not be a valid member of the family Pseudokeronopsidae.
 

The morphology, the infraciliature, some stages of cell division and physiological reorganization, and the SSU rRNA gene sequence of the little-known marine 18-cirri hypotrich Tachysoma rigescens (Kahl, 1932) Borror, 1972 [basionym Oxytricha (Tachysoma) rigescens], isolated from mariculture waters near Qingdao, China, were investigated. This rare species is characterized, inter alia, by narrowly spaced, small, colourless cortical granules and several conspicuous ring-shaped structures in the cytoplasm. The caudal cirri and the simple dorsal kinety pattern (three bipolar kineties) are probably plesiomorphic traits within the Hypotricha, the composition of the adoral zone of the proter from new and parental membranelles, as well as the presence of two ‘extra’ cirri behind the right marginal row strongly suggest a misclassification in Tachysoma. The SSU rRNA gene sequence data indicate that T. rigescens branches off rather basally in the Hypotricha tree, which supports the hypothesis that the 18-cirri pattern occurred very early, probably already in the last common ancestor of the Hypotricha. A detailed survey of the early branching 18-cirri hypotrichs and similar taxa (e.g. Trachelostyla pediculiformis, Hemigastrostyla enigmatica, Protogastrostyla pulchra) reveals that for T. rigescens a new genus (Apogastrostyla gen. nov.) has to be established, because there are important differences, inter alia, in the dorsal infraciliature. Besides the type species, A. rigescens comb. nov., which seems to be confined to the northern hemisphere according to the sparse faunistic data, a second marine species, A. szaboi comb. nov. (basionym Hemigastrostyla szaboi), so far only twice recorded from the Antarctic region, can be included. The Chinese population is fixed as neotype to define the species objectively, because no type material of A. rigescens is present and the original type locality is not known. The species name Tachysoma multinucleate is emended: Tachysoma multinucleatum nom. corr.

The largest known Aspidisca species, A. magna Kahl, 1932, was found from coastal waters near Qingdao (Tsingtao), northern China, and investigated using both the “wet” silver nitrate and protargol staining method. Based on the living observation and impregnated individuals, improved diagnosis and morphometric data are provided. As an additional contribution, the morphogenesis in Aspidisca magna during binary fission was revealed and summarized as follows: 1) the parental adoral zone of membranelles and paroral membranęare retained by the proter; 2) the oral primordium of the opisthe develops hypoapokinetally behind the posterior part of the adoral zone of membranelles; 3) five frontoventral-transverse cirral anlagen are formed de novo, initially as primary primordia, and develop into 3:3:2:2:1 cirri from left to right, respectively in both dividers; 4) the leftmost frontoventral cirrus is generated from an independently formed cirral anlage in both dividers. In the present work, Chinese and Korean populations of A. leptaspis Fresenius, 1865 were investigated respectively to support the importance of living characteristics in identification of Aspidisca species. The isolation of A. magna and A. leptaspis from other congeners are also firmly demonstrated by the SSU rRNA gene sequence alignments.

Euplotes balteatus (Dujardin, 1841) Kahl 1932, collected from coastal waters near Qingdao, northern China, was investigated using live observation and silver staining methods. An improved diagnosis and morphometric data are provided. Euplotes balteatus can be identified by the following combination of characters: 10 frontoventral cirri, 2 widely separated marginal cirri, 2 fine caudal cirri, 8 dorsal kineties and a double-eurystomus type silverline system. Its morphogenesis, which is similar to that of several congeners, can be summarized as follows: (1) the opisthe’s oral primordium appears de novo under the pellicle whereas the old oral apparatus is retained by the proter; (2) two groups of frontoventral transverse cirral anlagen, each with five streaks, occur de novo and then develop into the frontoventral and transverse cirri separately according to the formula of “3:3:3:3:2” from left to right; (3) the anlagen for the marginal cirri occur de novo near the parental oral apparatus; (4) migratory cirri of both dividers derive from the anlagen near the paroral membrane; (5) the dorsal kinety anlagen come from dedifferentiation of the parental structures in the mid-body region; (6) caudal cirri are formed at the posterior ends of the two rightmost dorsal kineties. In the light of the present findings, it was concluded that the Antarctic population of E. balteatus reported by Song and Wilbert (2002) was misidentified. A new species, Euplotes wilberti nov. spec., is established for this population.