• Animal Systematics, Evolution and Diversity
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• v.26 no.3
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• pp.217-221
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• 2010

Since November, 2006, the new creeping platyctenid ctenophore, Coeloplana anthostella n. sp., has been collected from twigs and polyp masses of encrusting dendronephthyans at a depth of 26-32 m off the coast of Munseom, Jejudo Island. This new species is distinguished from C. bocki Komai, 1920 and C. komai Utinomi, 1963 by its smaller size, the absence of dorsal papillae, and the deep scarlet colored star-shaped markings on the dorsal plane. This novel addition to ctenophore fauna is presently described and illustrated in detail.

• Animal Systematics, Evolution and Diversity
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• v.25 no.3
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• pp.255-259
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• 2009

The sessile ctenophores, Lyrocteis imperatoris Komai, 1941 were collected for the first time from Garinyeo, offshore Seogwipo of Jejudo Island by SCUBA diving on June 18, 2009. This species distributed in West North Pacific was newly recorded in Korean waters. Its embryos in various developmental stages were observed in the internal brood chamber.

• Animal Systematics, Evolution and Diversity
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• v.27 no.1
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• pp.47-52
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• 2011

Creeping ctenophores, Coeloplana species, were collected by SCUBA divers throughout the year (November 2006 to June 2010) from the branches and polyp masses of encrusting dendronephthyas at a depth of 20-32m off Munseom Island (Seogwipo-si, Jeju-do, Korea). A single individual of a newly recorded species in Korea, Coeloplana bocki Komai, 1920, was collected together with C. anthostella from the same location on 16 August 2009. A large number of individuals of each species were subsequently collected from the host Dendronephthya aff. dendritica on 20 June 2010. C. bocki can be distinguished from C. anthostella Song and Hwang, 2010 and C. komaii Utinomi, 1963 by its unique blue and orange colored stripes, and/or the branching and anastomosing milky-white stripes encircling the aboral sense organ towards the margin. The detailed morphology and molecular sequence information (nuclear 18S rDNA, internal transcribed spacer 1, and mitochondrial cox1 gene sequences) for C. bocki is provided, and C. bocki and C. anthostella are compared.

• 한국해양학회지
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• v.27 no.4
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• pp.268-276
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• 1992

Multitrophic interactions among gelatinous planktivores, zooplankton, and phytoplankton were in vestigated in Reeves Bay. New York from mid-March to July in 1989 to evaluate the top-down effect by gelatinous macrozooplankton on the Gyrodinium aureolum bloom through cascading tropic interactions. Zooplankton abundances reached maximal density following a decrease in gelatinous macrozooplankton (hydromedusae and scyphomedusae) abundances, and phytoplankton biomass was low at this time. Subsequently, as ctenophore populations increased zooplankton abundances decreased sharply, and the cell concnetration of G. aureolum began to increase. This field observation supports that the top-down control by gelatinous macrozooplankton on grazers, resulting in low grazing pressure on phytoplankton, can cause an algal bloom. The minimal zooplankton grazing measured using /SUP 14/C tracer technique during the bloom period indicated that zooplankton did not prefer G. aureolum as a good source.

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.12 no.3
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• pp.178-185
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• 2007

Myrionecta rubra Jankowski 1976(=Mesodinium rubrum Lohmann 1908), a mixotrophic ciliate, is very common and often causes recurrent red tides in diverse marine environments. Since the report on the first laboratory strain of this species in 2000, papers on its novel ecological role and evolutionary importance have been high lighted. This review paper is prepared to promote the de novo recognition M. rubra as a marine mixotrophic species. M. rubra is a ciliate which is able to photosynthesize using plastids originated from cryptophyte (including Teleaulax sp. and Geminigera sp.) prey cells (i.e. kleptoplastidic ciliate). Recently, novel bacterivory of M. rubra was firstly reported. Thus, the nutritional modes of M. rubra include photosynthesis, bacterivory, and algivory. In turn, M. rubra was reported as the prey species of metazoan predators such as calanoid copepods, mysids, larvae of ctenophore and anchovy, and spats of bivalves. In addition, it was reported that dinoflagellate Dinophysis causing diarrhetic shellfish poisoning is one among the predators of M. rubra. Thus, M. rubra, a marine mixotrophic ciliate, may play a pivotal role as a common linking ciliate for the flow of energy and organic material in pelagic food webs.