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Newly discovered role of the heterotrophic nanoflagellate Katablepharis japonica,a predator of toxic or harmful dinoflagellates and raphidophytes
Institution:1. Departament de Biologia Marina i Oceanografia. Institut de Ciències del Mar (CSIC). Pg. Marítim de la Barceloneta, 37-49 08003 Barcelona, Catalonia, Spain;2. Finnish Environment Institute (SYKE), Marine Research Laboratory, Agnes Sjöbergin katu 2, 00790 Helsinki, Finland;3. Department of Zoology, University of Oxford, 11a Mansfield Rd, Oxford, OX1 3SZ, United Kingdom;4. Leibniz Institute for Baltic Sea Research Warnemünde, Department of Biological Oceanography, Seestraße 15, 18119 Rostock, Germany
Abstract:Heterotrophic nanoflagellates are ubiquitous and known to be major predators of bacteria. The feeding of free-living heterotrophic nanoflagellates on phytoplankton is poorly understood, although these two components usually co-exist. To investigate the feeding and ecological roles of major heterotrophic nanoflagellates Katablepharis spp., the feeding ability of Katablepharis japonica on bacteria and phytoplankton species and the type of the prey that K. japonica can feed on were explored. Furthermore, the growth and ingestion rates of K. japonica on the dinoflagellate Akashiwo sanguinea—a suitable algal prey item—heterotrophic bacteria, and the cyanobacteria Synechococcus sp., as a function of prey concentration were determined. Among the prey tested, K. japonica ingested heterotrophic bacteria, Synechococcus sp., the prasinophyte Pyramimonas sp., the cryptophytes Rhodomonas salina and Teleaulax sp., the raphidophytes Heterosigma akashiwo and Chattonella ovata, the dinoflagellates Heterocapsa rotundata, Amphidinium carterae, Prorocentrum donghaiense, Alexandrium minutum, Cochlodinium polykrikoides, Gymnodinium catenatum, A. sanguinea, Coolia malayensis, and the ciliate Mesodinium rubrum, however, it did not feed on the dinoflagellates Alexandrium catenella, Gambierdiscus caribaeus, Heterocapsa triquetra, Lingulodinium polyedra, Prorocentrum cordatum, P. micans, and Scrippsiella acuminata and the diatom Skeletonema costatum. Many K. japonica cells attacked and ingested a prey cell together after pecking and rupturing the surface of the prey cell and then uptaking the materials that emerged from the ruptured cell surface. Cells of A. sanguinea supported positive growth of K. japonica, but neither heterotrophic bacteria nor Synechococcus sp. supported growth. The maximum specific growth rate of K. japonica on A. sanguinea was 1.01 d−1. In addition, the maximum ingestion rate of K. japonica for A. sanguinea was 0.13 ng C predator−1d−1 (0.06 cells predator−1d−1). The maximum ingestion rate of K. japonica for heterotrophic bacteria was 0.019 ng C predator−1d−1 (266 bacteria predator−1d−1), and the highest ingestion rate of K. japonica for Synechococcus sp. at the given prey concentrations of up to ca. 107 cells ml−1 was 0.01 ng C predator−1d−1 (48 Synechococcus predator−1d−1). The maximum daily carbon acquisition from A. sanguinea, heterotrophic bacteria, and Synechococcus sp. were 307, 43, and 22%, respectively, of the body carbon of the predator. Thus, low ingestion rates of K. japonica on heterotrophic bacteria and Synechococcus sp. may be responsible for the lack of growth. The results of the present study clearly show that K. japonica is a predator of diverse phytoplankton, including toxic or harmful algae, and may also affect the dynamics of red tides caused by these prey species.
Keywords:Feeding  Grazing  Growth  Harmful algal bloom  Ingestion  Red tide
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