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Colonization dynamics of periphytic ciliates at different water depths in coastal waters of the Yellow Sea, northern China

Published online by Cambridge University Press:  26 December 2018

Mohammad Nurul Azim Sikder ,
Mamun Abdullah Al Open the ORCID record for Mamun Abdullah Al [Opens in a new window] ,
Guobin Hu  and
Henglong Xu
Mohammad Nurul Azim Sikder
Affiliation:
College of Marine Life Sciences, Ocean University of China, Qingdao 266003, China
Mamun Abdullah Al
Affiliation:
College of Marine Life Sciences, Ocean University of China, Qingdao 266003, China
Guobin Hu
Affiliation:
College of Marine Life Sciences, Ocean University of China, Qingdao 266003, China Institute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao 266003, China
Henglong Xu*
Affiliation:
College of Marine Life Sciences, Ocean University of China, Qingdao 266003, China
*
Author for correspondence: Henglong Xu, E-mail: [email protected]
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Abstract

The colonization features of ciliate communities have proved to be a useful tool for indicating water quality status in aquatic ecosystems. To determine an optimal water depth for bioassessment using these ecological bioindicators, the colonization process of periphytic ciliates was studied at four depths of 1, 2, 3.5 and 5 m in Chinese coastal waters. Samples were collected at time intervals of 3, 7, 10, 14, 21 and 28 days using glass slides. The periphytic ciliate communities represented similar colonization dynamics from a depth of 1 to 3.5 m: (1) the temporal variability was well fitted to the MacArthur-Wilson and logistic models; (2) the species composition reached an equilibrium during the exposure time periods of 10–14 days; and (3) the maximum abundances were definitely higher at a depth of 1 m than those at 3.5 m. PERMANOVA test revealed that the colonization pattern at 1 m depth was significantly different from those at the other three depths. Results suggest that the colonization dynamics of periphytic ciliates may be influenced by water depth in coastal waters. These findings provide an important reference for establishing an optimal sampling strategy for bioassessment on large spatial/temporal scales in marine ecosystems.

Keywords

artificial substratumbioassessmentciliate communitiesmarine ecosystemsvertical variations
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 99 , Issue 5 , August 2019 , pp. 1065 - 1073
Copyright
Copyright © Marine Biological Association of the United Kingdom 2018 

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Footnotes

*

Co-first author: M.N.A. Sikder & M. Abdullah Al.

References

Abdullah Al, M, Gao, Y, Xu, G, Wang, Z and Xu, H (2017) Variations in the community structure of biofilm-dwelling protozoa at different depths in coastal waters of the Yellow Sea, northern China. Journal of the Marine Biological Association of the United Kingdom. doi: 10.1017/S0025315417001680.Google Scholar
Abdullah Al, M, Gao, Y, Xu, G, Wang, Z, Warren, A and Xu, H (2018) Trophic-functional patterns of biofilm-dwelling ciliates at different water depths in coastal waters of the Yellow Sea, northern China. European Journal of Protistology 63, 34–43.Google Scholar
Anderson, MJ, Gorley, RN and Clark, KR (2008) PREMANOVA + for PRIMER Guide to Software and Statistical Methods. Plymouth: PRIMER-E.Google Scholar
Bamforth, SS (1982) The variety of artificial substrates used for microfauna. In Cairns, J Jr (ed.), Artificial Substrates. Ann Arbor, MI: Ann Arbor Science Publishers, pp. 115–130.Google Scholar
Berger, H (1999) Monograph of the Oxytrichidae (Ciliophora, Hypotrichia). Dordrecht: Kluwer Academic Publishers.Google Scholar
Burkovskii, IV and Mazei, YA (2001) A study of ciliate colonization of unpopulated substrates of an estuary in the White Sea. Oceanology 41, 845–852.Google Scholar
Burkovskii, IV, Mazei, YA and Esaulov, AS (2011) Influence of the period of existence of a biotope on the formation of the species structure of a marine psammophilous ciliate community. Russian Journal of Marine Biology 37, 177–184.Google Scholar
Cairns, J Jr and Henebry, MS (1982) Interactive and noninteractive protozoa colonization process. In Cairns, J Jr (ed.), Artificial Substrates. Ann Arbor, MI: Ann Arbor Science Publishers, pp. 27–30.Google Scholar
Clarke, RK and Gorley, RN (2015) PRIMER 7; User Manual/Tutorial. Plymouth: PRIMER-E.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.Google Scholar
Eisenmann, H, Letsiou, I, Feuchtinger, A, Bersker, W, Mannweiler, E, Hutzler, P and Arnz, P (2001) Interception of small particles by flocculent structures, sessile ciliates and the basic layer of a wastewater biofilm. Applied and Environmental Microbiology 67, 4286–4292.Google Scholar
Franco, C, Esteban, G and Tellez, C (1998) Colonization and succession of ciliated protozoa associated with submerged leaves in a river. Limnologica 28, 275–283.Google Scholar
Kathol, M, Norf, H, Arndt, H and Weitere, M (2009) Effects of temperature increase on the grazing of planktonic bacteria by biofilm-dwelling consumers. Aquatic Microbial Ecology 55, 65–79.Google Scholar
Li, J, Xu, H, Lin, X and Song, W (2009) Colonization of periphytic ciliated protozoa on an artificial substrate in marinculture waters with notes on responses to environmental factors. Progress in Natural Science 19, 1235–1240.Google Scholar
MacArthur, R and Wilson, EO (1967) The Theory of Island Biogeography. Princeton, NJ: Princeton University Press, p. 203.Google Scholar
Mieczan, T (2010) Periphytic ciliates in three shallow lakes in eastern Poland: a comparative study between a phytoplankton-dominated lake, a phytoplankton-macrophyte lake and a macrophyte-dominated lake. Zoological Studies 49, 589–600.Google Scholar
Norf, H, Arndt, H and Weitere, M (2007) Impact of local temperature increase on the early development of biofilm-associated ciliate communities. Oecologia 151, 341–350.Google Scholar
Norf, H, Arndt, H and Weitere, M (2009 a) Effects of resource supplements on mature ciliate biofilms: an empirical test using a new type of flow cell. Biofouling 25, 769–778.Google Scholar
Norf, H, Arndt, H and Weitere, M (2009 b) Responses of biofilm-dwelling ciliate communities to planktonic and benthic resource enrichment. Microbial Ecology 57, 687–700.Google Scholar
Parry, JD (2004) Protozoan grazing of freshwater biofilms. Advances in Applied Microbiology 57, 167–196.Google Scholar
Peters, RH (1983) The Ecological Implication of Body-Size. Cambridge: Cambridge University Press.Google Scholar
Railkin, AI (1995) Heterotrophic flagellates on artificial substrates in the White Sea. Cytology 37, 951–957.Google Scholar
Scherwass, A, Fischer, Y and Arndt, H (2005) Detritus as a potential food source for protozoans: utilization of fine particulate plant detritus by heterotrophic flagellate, Chilomonas paramecium and a ciliate, Tetrahymena pyriformis. Aquatic Ecology 39, 439–455.Google Scholar
Song, W, Warren, A and Hu, X (2009) Free-living Ciliates in the Bohai and Yellow Seas. Beijing: Science Press.Google Scholar
Struder-Kypke, MC (1999) Periphyton and sephagnicolous protists of dystrophic bog lakes (Brandenburg, Germany) I. Annual cycles, distribution and comparison to other lakes. Limnologica 29, 393–406.Google Scholar
Wang, Q and Xu, H (2015) Colonization dynamics in trophic-functional patterns of biofilm-dwelling ciliates using two methods in coastal waters. Journal of the Marine Biological Association of the United Kingdom 95, 681–689.Google Scholar
Wang, Z, Xu, G, Zhao, L, Gao, Y, Abdullah Al, M and Xu, H (2017) A new method for evaluating defense of microalgae against protozoan grazing. Ecological Indicators 77, 261–266.Google Scholar
Weitere, M, Schmidt-Denter, K and Arndt, H (2003) Laboratory experiments on the impact of biofilms on the plankton of a large river. Freshwater Biology 48, 1983–1992.Google Scholar
Xu, H, Min, GS, Choi, JK, Jung, JH and Park, MH (2009 a) 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.Google Scholar
Xu, H, Min, GS, Choi, JK, Kim, SJ, Jung, JH and Lim, BJ (2009 b) 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.Google Scholar
Xu, H, Zhang, W, Jiang, Y, Zhu, M, Al-Rasheid, KAS, Warren, A and Song, W (2011) An approach to determining sampling effort for analyzing biofilm-dwelling ciliate colonization using an artificial substratum in coastal waters. Biofouling 27, 357–366.Google Scholar
Xu, H, Zhang, W and Jiang, Y (2014) Do early colonization patterns of periphytic ciliate fauna reveal environmental quality status in coastal waters? Environmental Science and Pollution Research 21, 7097–7112.Google Scholar
Zhang, W, Xu, H, Jiang, Y, Zhu, M and Al-Resheid, KA (2012) Colonization dynamics in trophic-functional structure of periphytic protist communities in coastal waters. Marine Biology 159, 735–748.Google Scholar
Zhang, W, Xu, H, Jiang, Y, Zhu, M and Al-Rashied, KAS (2013) Colonization dynamics of periphytic ciliate communities on an artificial substratum in coastal waters of the Yellow Sea, northern China. Journal of the Marine Biological Association of the United Kingdom 93, 57–68.Google Scholar
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