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Colonization dynamics of periphytic ciliate communities across taxonomic levels using an artificial substrate for monitoring water quality in coastal waters

Published online by Cambridge University Press:  02 November 2010

Henglong Xu ,
Joon-Ki Choi ,
Gi-Sik Min  and
Qinglin Zhu
Henglong Xu
Affiliation:
Laboratory of Protozoology, Institute of Evolution and Marine Biodiversity, Ocean University of China, Qingdao 266003, China
Joon-Ki Choi*
Affiliation:
Department of Oceanography, Inha University, Incheon 402-751, Korea
Gi-Sik Min
Affiliation:
Department of Biological Sciences, Inha University, Incheon 402-751, Korea
Qinglin Zhu
Affiliation:
College of Physical and Environmental Oceanography, Ocean University of China, Qingdao 266100, China
*
Correspondence should be addressed to: J.K. Choi, Department of Oceanography, Inha University, Incheon 402-751, Korea email: [email protected]
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Abstract

Taxonomic diversity and temporal patterns in abundance of periphytic ciliate communities across taxonomic levels were studied to monitor water quality in Korean coastal waters during April 2007. Specifically we compared two methods based on an artificial substrate (glass slide): the polyurethane foam enveloped slide (PFES) and the conventional slide (CS) systems. The results demonstrated that: (1) the colonization patterns of the ciliate communities at all taxonomic levels showed a lower variability in the PFES system than those of the CS system; (2) The taxonomic diversity (Δ) and taxonomic distinctness (Δ*) were significantly higher in the PFES system than those in the CS system; and (3) all four taxonomic diversity/distinctness indices represented lower variability in the PFES system than those of the CS samples. These findings suggest that the PFES system is more effective than the CS system for measuring the colonization patterns and taxonomic distinctness parameters that are increasingly used as potential indicators of water quality. This conclusion supports our previous suggestion that the PFES system is a better tool than the CS system for monitoring water quality in the marine ecosystem, using periphytic ciliates.

Keywords

artificial substratebioassessmentmarine biofilmperiphytic ciliatetaxonomic diversity
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 91 , Issue 1 , February 2011 , pp. 91 - 96
Copyright
Copyright © Marine Biological Association of the United Kingdom 2010

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References

REFERENCES

Cairns, J. Jr and Henebry, M.S. (1982) Interactive and non-interactive protozoa colonization process. In Cairns, J. Jr(ed.)Artificial substrates. Ann Arbor, MI: Ann Arbor Science Publishers.Google Scholar
Cairns, J. Jr and Yongue, W.H. Jr (1968) The distribution of freshwater protozoa on a relatively homogenous substrate. Hydrobiologia 31, 65–72.CrossRefGoogle Scholar
Cairns, J. Jr, Lanza, G.R. and Parker, B.C. (1972) Pollution related to structural and functional changes in aquatic communities with emphasis on freshwater algae and protozoa. Proceedings of the Academy of Natural Sciences of Philadelphia 124, 79–127.Google Scholar
Clarke, K.R. and Warwick, R.M. (1998) A taxonomic distinctness index and its statistical properties. Journal of Applied Ecology 35, 523–531.CrossRefGoogle Scholar
Clarke, K.R. and Gorley, R.N. (2006) Primer V6. User manual/turorial. Plymouth: PRIMER-E Ltd.Google Scholar
Coppellotti, O. and Matarazzo, P. (2000) Ciliate colonization of artificial substrates in the Lagoon of Venice. Journal of the Marine Biological Association of the United Kingdom 80, 419–427.CrossRefGoogle Scholar
Corliss, J.O. (1979) The ciliated protozoa. Characterization, classification and guide to the literature. 2nd edition.Oxford: Pergamon Press.Google Scholar
Finlay, B.J. and Esteban, G.F. (1998) Freshwater protozoa: biodiversity and ecological function. Biodiversity and Conservation 7, 1163–1186.CrossRefGoogle Scholar
Franco, C., Esteban, G. and Téllez, C. (1998) Colonization and succession of ciliated protozoa associated with submerged leaves in a river. Limnologica 28, 275–283.Google Scholar
Gong, J., Song, W. and Warren, A. (2005) Periphytic ciliate colonization: annual cycle and responses to environmental conditions. Aquatic Microbial Ecology 39, 159–170.CrossRefGoogle Scholar
Leonard, D.R.P., Clarke, K.R., Somerfield, P.J. and Warwick, R.M. (2006) The application of an indicator based on taxonomic distinctness for UK marine biodiversity assessment. Journal of Environmental Management 78, 52–62.CrossRefGoogle Scholar
MacArthur, R. and Wilson, E.O. (1967) The theory of island biogeography. Princeton, NJ: Princeton University Press.Google Scholar
Mouillot, D., Gaillard, S., Aliaume, C., Verlaque, M. and Belsher, T. (2005) Ability of taxonomic diversity indices to discriminate coastal lagoon environment based on macrophyte communites. Ecological Indicators 5, 1–17.CrossRefGoogle Scholar
Munawar, M. and Weisse, T. (1989) Is the ‘microbial loop’ an early warning indicator of anthropogenic stress? Hydrobiologia 188/189, 163–174.CrossRefGoogle Scholar
Norf, H., Arndt, H. and Weitere, M. (2007) Impact of local temperature increase on the early development of biofilim-associated ciliate communities. Oecologia 151, 341–350.CrossRefGoogle ScholarPubMed
Norf, H., Arndt, H. and Weitere, M. (2009) Effects of resource supplements on mature ciliate biofilms: an empirical test using a new type of flow cell. Biofouling 25, 769–778.CrossRefGoogle ScholarPubMed
Prato, S., Morgana, J.G., Valle, P.La, Finoiaand, M.G. and Lattanzi, L. (2009) Application of biotic and taxonomic distinctness indices in assessing the ecological quality status of two coastal lakes: Gaprolace and Foglino Lakes (Central Italy). Ecological Indicators 9, 568–583.CrossRefGoogle Scholar
Warwick, R.M. and Clarke, K.R. (1995) New ‘biodiversity’ measures reveal a decrease in taxonomic distinctness with increasing stress. Marine Ecology Progress Series 129, 301–305.CrossRefGoogle Scholar
Warwick, R.M. and Clarke, K.R. (2001) Practical measures of marine biodiversity based on relatedness. Oceanography and Marine Biology: an Annual Review 39, 207–231.Google Scholar
Xu, K., Choi, J.K., Yang, E.J., Lee, K.C. and Lei, Y. (2002) Biomonitoring of coastal pollution status using protozoan communities with a modified PFU method. Marine Pollution Bulletin 44, 877–886.CrossRefGoogle ScholarPubMed
Xu, M., Gao, H., Xie, P., Deng, D., Feng, W. and Xu, J. (2005) Use of PFU protozoa community structural and functional characteristics in assessment of water quality in a large, highly polluted freshwater lake in China. Journal of Environmental Monitoring 7, 670–674.CrossRefGoogle Scholar
Xu, H., Min, G.K., Choi, J.K., Jung, J.H. and Park, M.H. (2009a) An approach to analyses of periphytic ciliate colonization for monitoring water quality using a modified artificial substrate in Korean coastal waters. Marine Pollution Bulletin 58, 1278–1285.CrossRefGoogle ScholarPubMed
Xu, H., Min, G.K., Choi, J.K., Kim, S.J., Jung, J.H. and Lim, B.J. (2009b) An approach to analyses of periphytic ciliate communities for monitoring water quality using a modified artificial substrate in Korean coastal waters. Journal of the Marine Biological Association of the United Kingdom 89, 669–679.CrossRefGoogle Scholar