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Diel patterns of grazing by pigmented nanoflagellates on Synechococcus spp. in the coastal ecosystem of subtropical western Pacific

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Abstract

Natural populations of planktonic Synechococcus spp. exhibit diel variations in abundance and frequency of dividing cells (FDC) during the warm seasons (>25°C) in coastal water of the western subtropical Pacific ocean. We hypothesized that differences in grazing rates during the day/dark cycle were a major cause of the observed diel variations in Synechococcus spp. abundance. We used fluorescently labeled particles (FLP) as tracers of feeding on Synechococcus spp. in June and August 2007. Our results showed that FDC of Synechococcus spp. were highest at dusk (50%) and lowest (<10%) between midnight and early morning. Synechococcus spp. had three abundance phases, accrual (I), peak (II), and diminished (III). Moreover, FDC values gradually increased in phase I, declined to the lowest values during phase II, and remained at low levels throughout phase III. Our results strongly indicated that pigmented nanoflagellate (PNF) grazing was the underlying biological factor regulating diel variations in Synechococcus spp. abundance. And, the rate of PNF ingestion peaked during the night on smaller non-dividing cells following a peak of Synechococcus spp. abundance in phase II. These findings provide evidence that diel variations in ingestion rates are affected by non-dividing cells of Synechococcus spp. and imply that the impacts of PNF grazing on Synechococcus spp. is based on food selectivity by size.

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References

  • Agawin, N. S. R., C. M. Duarte & S. Agustí, 2000. Nutrient and temperature control of the contribution of picoplankton to phytoplankton biomass and production. Limnology and Oceanography 45(3): 591–600.

    CAS  Google Scholar 

  • Andersson, A., P. Haecky & A. Hagström, 1994. Effect of temperature and light on the growth of micro- nano- and picoplankton: impact on algal succession. Marine Biology 120: 511–520.

    Article  Google Scholar 

  • Blanchot, J. & M. Rodier, 1996. Picophytoplankton abundance and biomass in the western tropical Pacific Ocean during the 1992 EI Niño year: results from flow cytometry. Deep-Sea Research 43: 877–895.

    Article  Google Scholar 

  • Callieri, C., S. M. Karjalainen & S. Passoni, 2002. Grazing by ciliates and heterotrophic nanoflagellates on picocyanobacteria in Lago Maggiore, Italy. Journal of Plankton Research 24: 785–796.

    Article  Google Scholar 

  • Caron, D. A., E. L. Lim, G. Miceli, J. B. Waterbury & F. W. Valois, 1991. Grazing and utilization of chroococcoid cyanobacteria and heterotrophic bacteria by protozoa in laboratory cultures and a coastal plankton community. Marine Ecology Progress Series 76: 205–217.

    Article  Google Scholar 

  • Chan, Y. F., A. Y. Tsai, K. P. Chiang & C. H. Hsieh, 2009. The grazing impact of the different size of pigmented nanoflagellates on Synechococcus in the coastal ecosystem of subtropical western Pacific. Microbial Ecology. doi:10.1007/s00248-009-9569-x.

  • Chang, J., C. C. Chung & G. C. Gong, 1996. Influences of cyclones on chlorophyll a concentration and Synechococcus abundance in a subtropical western Pacific coastal ecosystem. Marine Ecology Progress Series 140: 199–205.

    Article  Google Scholar 

  • Choi, J. W., 1994. The dynamic nature of protistan ingestion response to prey abundance. The Journal of Eukaryotic Microbiology 41: 137–146.

    Article  Google Scholar 

  • Christaki, U., A. Giannakourou, F. Van Wanbeke & G. Grégori, 2001. Nanoflagellate predation on auto- and heterotrophic picoplankton in the oligotrophic Mediterranean Sea. Journal of Plankton Research 23: 1297–1310.

    Article  Google Scholar 

  • Christaki, U., C. Courties, H. Karayanni, A. Giannakouron, C. Maravelias, A. K. Kormas & P. Lebaron, 2002. Dynamic characteristics of Prochlorococcus and Synechococcus consumption by bacterivorous nanoflagellates. Microbial Ecology 43: 341–352.

    Article  CAS  PubMed  Google Scholar 

  • Dolan, J. R. & K. Šimek, 1999. Diel periodicity in Synechococcus populations and grazing by heterotrophic nanoflagellates: analysis of food vacuole contents. Limnology and Oceanography 44(6): 1565–1570.

    Google Scholar 

  • Epstein, S. S. & M. Shiaris, 1992. Size-selective grazing of coastal bacterioplankton by natural assemblages of pigmented flagellates, colorless flagellates, and ciliates. Microbial Ecology 23: 211–225.

    Article  Google Scholar 

  • Hall, J. A., D. P. Barrett & M. R. James, 1993. The importance of phytoflagellate, heterotrophic flagellate and ciliate grazing on bacteria and picophytoplankton sized prey in a coastal marine environment. Journal of Plankton Research 15: 1075–1086.

    Article  Google Scholar 

  • Jacquet, S., D. Lennon, D. Marie & D. Vaulot, 1998. Picoplankton population dynamics in coastal waters of the N. W. Mediterranean Sea. Limnology and Oceanography 43: 1916–1931.

    CAS  Google Scholar 

  • Johnson, P. W. & J. M. Sieburth, 1979. Chroococcoid cyanobacteria in the sea: a ubiquitous and diverse phytotrophic biomass. Limnology and Oceanography 24: 928–935.

    Google Scholar 

  • Jürgens, K. & H. Güde, 1994. The potential importance of grazing-resistant bacteria in planktonic systems. Marine Ecology Progress Series 112: 169–188.

    Article  Google Scholar 

  • Li, W. K. W., 1998. Annual average abundance of heterotrophic bacteria and Synechococcus in surface ocean waters. Limnology and Oceanography 43: 1746–1753.

    Article  Google Scholar 

  • Olson, R. J., S. W. Chisholm, E. R. Zettler & E. R. Armbrust, 1990. Pigments, size, and distribution of Synechococcus in the North Atlantic and Pacific Oceans. Limnology and Oceanography 35(1): 45–58.

    Article  CAS  Google Scholar 

  • Pace, M. L. & M. D. Bailiff, 1987. Evaluation of a fluorescent microsphere technique for measuring grazing rates of phagotrophic microorganisms. Marine Ecology Progress Series 40: 185–193.

    Article  Google Scholar 

  • Partensky, F., W. R. Hess & D. Vaulot, 1999. Prochlorococcus, a marine photosynethetic prokaryote of global significance. Mirobiology and Molecular Biology Reviews 63: 106–127.

    CAS  Google Scholar 

  • Porter, K. G. & Y. S. Feig, 1980. The use of DAPI for identifying and counting aquatic microflora. Limnology and Oceanography 25: 943–948.

    Article  Google Scholar 

  • Safi, K. A. & J. A. Hall, 1999. Mixotrophic and heterotrophic nanoflagellate grazing in the convergence zone east of New Zealand. Aquatic Microbial Ecology 20: 83–93.

    Article  Google Scholar 

  • Sanders, R. W. & K. G. Porter, 1988. Phagotrophic phytoflagellates. Advances in Microbial Ecology 10: 167–192.

    Google Scholar 

  • Sanders, R. W., U. G. Berninger, E. L. Lim, P. F. Kemp & D. A. Caron, 2000. Heterotrophic and mixotrophic nanoplankton predation on picoplankton in the Sargasso Sea and on Georges Bank. Marine Ecology Progress Series 192: 103–118.

    Article  Google Scholar 

  • Tsai, A. Y., K. P. Chiang, J. Chang & G. C. Gong, 2005. Seasonal diel variations of picoplankton and nanoplankton in a subtropical western Pacific coastal ecosystem. Limnology and Oceanography 50(4): 1221–1231.

    Article  CAS  Google Scholar 

  • Tsai, A. Y., K. P. Chiang, Y. F. Chan, Y. C. Lin & J. Chang, 2007. PNF in the coastal western subtropical Pacific are important grazers on Synechococcus populations. Journal of Plankton Research 29: 71–77.

    Article  Google Scholar 

  • Vaulot, D. & D. Marie, 1999. Diel variability of photosynthetic picoplankton in the Equatorial Pacific. Journal of Geophysical Research 104: 3297–3310.

    Article  CAS  Google Scholar 

  • Waterbury, J. B., S. W. Watson, F. W. Valois & D. G. Franks, 1986. Biological and ecological characterization of the marine unicellular cyanobacterium Synechococcus. In Platt, T. & W. K. W. Li (eds), Photosynethetic picoplankton. Canadian Bulletin Journal of Fisheries Aquatic Sciences 214: 71–120.

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Acknowledgments

This study was supported by a grant (NSC 95-2611-M-019-022-MY3) from the National Science Council, ROC. We are most grateful to Dr. Sanders for his language editing on the manuscript.

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Correspondence to Kuo-Ping Chiang.

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Handling editor: D. Bade

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An-Yi, T., Chin, WM. & Chiang, KP. Diel patterns of grazing by pigmented nanoflagellates on Synechococcus spp. in the coastal ecosystem of subtropical western Pacific. Hydrobiologia 636, 249–256 (2009). https://doi.org/10.1007/s10750-009-9954-y

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