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Structural parameters of periphytic ciliate communities on a modified substrate were studied in Korean coastal waters during the period August -November 2007. In order to reduce the strong disturbances from tidal current and circulation in marine ecosystems, a modified slide method, named the polyurethane foam enveloped slide (PFES) system, was used to host ciliate communities. A total of 37 ciliate species, about half of which belong to the orders Hypotrichida and Cyrtophorida, were identified using living observation and silver impregnation method with this system. The sessile ciliates belonged to the orders Peritrichida and Suctorida, while the motile forms were represented primarily by the species of the orders Hypotrichida, Cyrtophorida and Pleurostomatida. The species diversity and evenness were significantly higher in the PFES system than those on the conventional slides (paired t-test: t ¼ 2.384, 2.415; P , 0.05). Multivariate analysis revealed that the ciliate communities from both sampling systems had similar species composition, but represented significant differences in species distribution and temporal dynamics mainly due to the most dominant peritrich Zoothaminium duplicatum, which overly colonized the conventional slides. Results suggest that the PFES system is more effective than the conventional slide method for periphytic ciliate colonization with high species diversity, evenness and sensitive temporal dynamics mainly due to the reduction of disturbances from tidal current and circulation in marine ecosystems.

The syndinean dinoflagellate Euduboscquella costata n. sp., an intracellular parasite of the tintinnid ciliate Schmidingerella arcuata, was discovered from Korean coastal water in November of 2013. Euduboscquella costata parasitized in about 62% of the host population, with infection intensity (= number of trophonts in a single host cell) ranging from 1 to 8. Based on morphology and nuclear 18S ribosomal RNA gene sequences, the parasite is new to science. Euduboscquella costata n. sp. had an infection cycle typical of the genus, but had morphological and developmental features that distinguished it from congeneric species. These features include: (1) episome of the trophont with 25-40 grooves converging toward the center of the shield; (2) a narrow, funnel-shaped lamina pharyngea extending from the margin of the episomal shield to the nucleus; (3) persistence of grooves during extracellular development (sporogenesis); (4) a single food vacuole during sporogenesis; (5) separation of sporocytes early in sporogenesis, regardless of type of spore formed; and (6) dinospore size (ca. 14 μm in length) and shape (bulbous episome with narrower, tapering hyposome). After sporogenesis, E. costata produced four different types of spore that showed completely identical 18S rRNA gene sequences. The gene sequence was completely identical with a previously reported population, Euduboscquella sp. ex S. arcuata, from Assawoman Bay, USA, indicating that the two populations are likely conspecific. Favella ehrenbergii, a widely recorded tintinnid known to host Euduboscquella spp., co-occurred with S. arcuata, but was not infected by E. costata in field samples or during short-term, cross-infection experiments.

Ciliates are a diverse species group of the Protozoa, and nuclear and mitochondrial genes have been utilized to discover new species and discriminate closely related species. The mitochondrial cytochrome c oxidase subunit 1 (CO1) gene has been used to discriminate metazoan species and has also been applied for some groups in the phylum Ciliophora. However, it is difficult to produce a universal primer as a standard barcode, because unlike metazoans, mitochondrial DNA sequences of ciliates are long and highly variable. Therefore, to design the new primer set, we sequenced the mitochondrial genomes of two pseudokeronopsids in the class Spirotrichea using next-generation sequencing technology (HiSeq™ 2000). Based on putative CO1 gene fragments of the pseudokeronopsids, we designed the new primer set and successfully sequenced the CO1 of 69 populations representing 47 species (five orders, 14 families, and 27 genera). We found that CO1 showed higher resolution for separating congeneric species than did nuclear SSU rRNA gene sequences, and we identified some putative cryptic species.

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