Kuidong Xu

There is a widespread belief that spathidiids have few morphological features. In contrast, we show a rich morphological diversity in five new species discovered in tank bromeliads from the Caribbean, using live observation; protargol impregnation; morphometry; scanning electron microscopy; and resting cyst morphology, demonstrating lepidosomes (organic scales) for the first time in spathidiid haptoria. Arcuospathidium bromelicola nov. spec. is very similar to the previously described A. muscorum but its resting cyst has conspicuous, pillar-shaped lepidosomes on the surface. Protospathidium lepidosomatum nov. spec. is very similar to the previously described P. muscicola but has outstanding, nipple-shaped (vs. conical) lepidosomes on the cyst surface. Spathidium bromeliophilum nov. spec., whose ontogenesis is highly similar to that of S. turgitorum, differs from similar species by the body length:width ratio, the number of ciliary rows, the shape of the oral bulge, and details of the ciliary pattern. Spathidium bromelicola nov. spec. is similar to S. muscicola (extrusomes bluntly fusiform and 4 µm long vs. rod-shaped and > 15 µm long) and S. stammeri (resting cyst wall smooth vs. spinous). Spathidium wolfi nov. spec. has an anterior and a posterior contractile vacuole. It differs from the supposed nearest relative, S. faurefremieti, by body size (on average 135 × 25 µm vs. 240 × 17 µm), the shape of the macronucleus (moniliform vs. a long, tortuous strand), and the total number of dorsal brush bristles (on average 47 vs. 72). The bent oral bulge of Arcuospathidium bromelicola and Spathidium bromeliophilum as well as the occurrence of lepidosomes on the cyst surface of Arcuospathidium bromelicola and Protospathidium lepidosomatum are discussed.

The morphology and taxonomy of two new and two poorly known ciliate species of Ancistrum, found in the mantle cavity (mainly on gills) of marine molluscs from culture beds and pools along the Chinese coast of the Yellow Sea, were investigated using living observation and silver impregnation. Ancistrum haliotis n. sp. was isolated from the abalone Haliotis discus hannai Ino, A. crassum Fenchel, 1965 from the purple clam Saxidomus purpuratus (Sowerby), A. acutum n. sp. from the surf clam Mactra veneriformis Reeve, and A. japonicum Uyemura, 1937 from both the venus clam Cyclina sinensis (Gmelin) and from Dosinia japonica (Reeve). Ancistrum haliotis differs from its most similar relative A. mytili (Quennerstedt, 1867) by the body outline (anterior portion narrower vs. wider than the posterior portion), the macronuclear shape (broadly ellipsoidal vs. reniform or sausage-like), and by having fewer somatic kineties (28–32 vs. usually more than >40). Ancistrum crassum is characterized by the naked area at the apical end of the cell, the relatively short buccal field occupying about two thirds of the body length, and the posterior-dorsal cone-shaped prolongation. Ancistrum acutum n. sp. and A. japonicum are almost identical in morphometry, but differ distinctly in the live morphology (anterior end pointed and posterior end rounded vs. anterior end narrowly rounded and posterior-dorsal end protruded) and ciliary pattern (all right-side kineties extend to posterior body end vs. all right-side kineties excluding somatic kinety 1 distinctly shortened posteriad, forming a glabrous zone). We neotypify Ancistrum japonicum and discuss the taxonomic status of the four species. Based on an evaluation of all nominal species of Ancistrum and Ancistrumina, we recognize nine valid species of Ancistrum and provide a tabular guide to their identification. Fenchelia Raabe, 1970 is regarded as a junior synonym of Ancistrum Maupas, 1883. We synonymize Ancistrumina nucellae Khan, 1970 with Ancistrum japonicum Uyemura, 1937 and Ancistrum edajimanum Oishi, 1978 with A. crassum Fenchel, 1965.