Hostname: page-component-586b7cd67f-t7fkt Total loading time: 0 Render date: 2024-11-24T01:22:23.276Z Has data issue: false hasContentIssue false
  • English
  • Français

Temporal variation in body-size spectrum of biofilm-dwelling protozoa during the colonization process in coastal waters of the Yellow Sea, northern China

Published online by Cambridge University Press:  11 March 2016

Zheng Wang ,
Guanjian Xu  and
Henglong Xu
Zheng Wang
Affiliation:
Department of Marine Ecology, Ocean University of China, Qingdao 266003, China Department of Marine Biology, Ocean University of China, Qingdao 266003, China
Guanjian Xu
Affiliation:
Department of Marine Ecology, Ocean University of China, Qingdao 266003, China Department of Marine Biology, Ocean University of China, Qingdao 266003, China
Henglong Xu*
Affiliation:
Department of Marine Ecology, Ocean University of China, Qingdao 266003, China
*
Correspondence should be addressed to:H. Xu, Department of Marine Ecology, Ocean University of China, Qingdao 266003, China email: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

As an inherent function of a community, body-size spectrum has been increasingly used as a useful indicator in global ecological research. The colonization dynamics of biofilm-dwelling protozoa with regard to body-size spectrum were studied based on a 1-month baseline survey in coastal waters of the Yellow Sea, northern China. Samples were collected at time intervals of 1, 3, 7, 10, 14, 21 and 28 days from depths of 1 and 3 m. A total of seven body-size ranks were identified based on a trait hierarchy. The individual abundance of the protozoa at each body-size rank was well fitted to the logistic model equation. The body-size spectra showed a clear shift in probability density during the colonization period at both depths. The multivariate approach demonstrated that the temporal dynamics in body-size spectra of the protozoa may be divided into initial (1 day), transitional (3–7 days) and stable (10–28 days) stages during the colonization period. These results provide useful information for ecological research and monitoring programmes using biofilm-dwelling protozoa in marine ecosystems.

Keywords

biofilm-dwelling protozoabody-size spectrumfield communityfunctional ecologycolonization survey
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 96 , Issue 5 , August 2016 , pp. 1113 - 1118
Copyright
Copyright © Marine Biological Association of the United Kingdom 2016 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Anderson, M.J., Gorley, R.N. and Clarke, K.R. (2008) PERMANOVA+ for PRIMER guide to software and statistical methods. Plymouth: PRIMER-E.Google Scholar
Clarke, K.R. and Gorley, R.N. (2015) PRIMER 7: user manual/tutorial. Plymouth: PRIMER-E.Google Scholar
Dolbeth, M., Raffaelli, D. and Pardal, M.Â. (2014) Patterns in estuarine macrofauna body size distributions: the role of habitat and disturbance impact. Journal of Sea Research 85, 404–412.Google 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
Früh, D., Norf, H. and Weitere, M. (2011) Response of biofilm-dwelling ciliate communities to enrichment with algae. Aquatic Microbial Ecology 63, 299–309.Google Scholar
George, P.B.L. and Lindo, Z. (2015) Application of body size spectra to nematode trait-index analyses. Soil Biology and Biochemistry 84, 15–20.Google Scholar
Jiang, Y., Xu, H., Zhang, W., Zhu, M. and Al-Rasheid, K.A.S. (2012) Can body-size patterns of ciliated zooplankton be used for assessing marine water quality? A case study on bioassessment in Jiaozhou Bay, northern Yellow Sea. Environmental Science and Pollution Research 19, 1747–1754.Google Scholar
Kamenir, Y., Dubinsky, Z. and Harris, R. (2010) Taxonomic size structure consistency of English Channel phytoplankton. Journal of Experimental Marine Biology and Ecology 383, 105–110.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
Kiørboe, T., Grossart, H.P., Ploug, H., Tang, K. and Auer, B. (2004) Particle-associated flagellates: swimming patterns, colonization rates, and grazing on attached bacteria. Aquatic Microbial Ecology 35, 141–152.Google Scholar
Krupica, K.L., Sprules, W.G. and Herman, A.W. (2012) The utility of body size indices derived from optical plankton counter data for the characterization of marine zooplankton assemblages. Continental Shelf Research 36, 29–40.Google Scholar
Liu, T., Guo, R., Ran, W., Whalem, J.K. and Li, H. (2015) Body size is a sensitive trait-based indicator of soil nematode community response to fertilization in rice and wheat agroecosystems. Soil Biology and Biochemistry 88, 275–281.Google Scholar
Morin, S., Pesce, S., Tlili, A., Coste, M. and Montuelle, B. (2010) Recovery potential of periphytic communities in a river impacted by a vineyard watershed. Ecological Indicators 10, 419–426.CrossRefGoogle Scholar
Norf, H., Arndt, H. and Weitere, M. (2009a) Responses of biofilm-dwelling ciliate communities to planktonic and benthic resource enrichment. Microbial Ecology 57, 687–700.CrossRefGoogle ScholarPubMed
Norf, H., Arndt, H. and Weitere, M. (2009b) Effects of resource supplements on mature ciliate biofilms: an empirical test using a new type of flow cell. Biofouling 25, 769–778.Google Scholar
Railkin, A.I. (1995) Heterotrophic flagellates on artificial substrates in the White Sea. Cytology 37, 951–957.Google Scholar
San Martin, E., Harris, R.P. and Irigoien, X. (2006) Latitudinal variation in plankton size spectra in the Atlantic Ocean. Deep Sea Research Part II: Topical Studies in Oceanography 53, 1560–1572.CrossRefGoogle Scholar
Sheldon, R.W., Prakash, A. and Sutcliffe, W.H. (1972) The size distribution of particles in the ocean. Limnology and Oceanography 17, 327–340.Google Scholar
Song, W., Warren, A. and Hu, X. (2009) Free-living ciliates in the Bohai and Yellow Seas, China. Beijing: Science Press. [In both Chinese and English]Google Scholar
Wey, J.K., Norf, H., Arndt, H. and Weitere, M. (2009) Role of dispersal in shaping communities of ciliates and heterotrophic flagellates within riverine biofilms. Limnology and Oceanography 54, 1615–1626.Google Scholar
Winberg, G.G. (1971) Methods for the estimation of production of aquatic animals. New York, NY: Academic Press.Google Scholar
Xu, G., Zhang, W. and Xu, H. (2015a) Can dispersions be used for discriminating water status in coastal ecosystems? A case study on biofilm-dwelling microbial eukaryotes. Ecological Indicators 57, 208–214.Google Scholar
Xu, G., Zhang, W. and Xu, H. (2015b) An approach to bioassessment of water quality using diversity measures based on species accumulative curves. Marine Pollution Bulletin 91, 238–242.Google Scholar
Xu, G., Zhao, L., Zhang, W. and Xu, H. (2015c) Identifying homogeneity of multivariate dispersion among biofilm-dwelling microbial communities in colonization surveys for marine bioassessment. Ecological Indicators 58, 32–36.Google Scholar
Xu, G., Zhong, X., Wang, Y. and Xu, H. (2015d) An approach to determination of optimal species pool of periphytic microfauna in colonization surveys for marine bioassessment. Environmental Science and Pollution Research 22, 7967–7972.Google Scholar
Xu, G., Zhong, X., Wang, Y. and Xu, H. (2014a) A multivariate approach to the determination of an indicator species pool for community-based bioassessment of marine water quality. Marine Pollution Bulletin 87, 147–151.Google Scholar
Xu, H., Jiang, Y., Zhang, W., Zhu, M., Al-Rasheid, K.A.S. and Warren, A. (2013) Annual variations in body-size spectra of planktonic ciliate communities and their relationships to environmental conditions: a case study in Jiaozhou Bay, northern China. Journal of the Marine Biological Association of the United Kingdom 93, 47–55.Google Scholar
Xu, H., Zhang, W. and Jiang, Y. (2014b) 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
Xu, H., Zhang, W., Jiang, Y. and Yang, E.J. (2014c) Use of biofilm-dwelling ciliate communities to determine environmental quality status of coastal water. Science of the Total Environment 470–471, 511–518.Google Scholar
Xu, H., Zhang, W., Jiang, Y., Zhu, M. and Al-Resheid, K.A.S. (2012) An approach to analyzing influence of enumeration time periods on detecting ecological features of microperiphyton communities for marine bioassessment. Ecological Indicators 18, 50–57.Google Scholar
Xu, H., Zhang, W., Jiang, Y., Zhu, M., Al-Rasheid, K.A.S., 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
Zhang, W., Xu, H., Jiang, Y., Zhu, M. and Al-Reshaid, K.A.S. (2012a) 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-Reshaid, K.A.S. (2012b) Influence of enumeration time periods on analyzing colonization features and taxonomic relatedness of periphytic ciliate communities using an artificial substratum for marine bioassessment. Environmental Science and Pollution Research 19, 3619–3627.Google Scholar
Supplementary material: File

Wang et al. supplementary material

Supplementary tables

Download Wang et al. supplementary material(File)
File 173.1 KB