JPR Advance Access originally published online on June 28, 2004
Journal of Plankton Research 2004 26(11):1289-1299; doi:10.1093/plankt/fbh120
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Journal of Plankton Research Vol. 26 No. 11 © Oxford University Press 2004; all rights reserved
Feeding of planktonic rotifers on ciliates: a method using natural ciliate assemblages labelled with fluorescent microparticles
University of Liège, Laboratory of Animal Ecology and Ecotoxicology, Quai van Beneden 22, B-4020 Liège, Belgium
* Corresponding Author: celia.joaquim-justo{at}ulg.ac.be
Received June 2, 2003; accepted in principle April 7, 2004; accepted for publication June 17, 2004; published online June 28, 2004
A method was developed to allow direct measurements of predation exerted by metazooplankton on ciliates. The method relied on the use of ciliates labelled with fluorescent microparticles (FMP). Optimal labelling conditions were determined with ciliates from cultures (Tetrahymena pyriformis) and with natural ciliate assemblages sampled in a river. Labelled T. pyriformis were used as tracer food to determine gut passage time (GPT) and ingestion rates of the rotifer Brachionus calyciflorus in the laboratory. Predation of metazooplankton from the lowland river Meuse (Belgium) was determined by labelling natural assemblages of ciliates and using them as tracer food for metazooplankters sampled in the river. Optimal labels of ciliates, i.e. sharp distribution of FMP in cells, were obtained with short incubations (10 min) and low FMP concentrations (1 x 105 mL–1). GPT varied between 30 and 45 min for B. calyciflorus and from 25 up to >35 min for rotifers from the river. The ingestion rate of B. calyciflorus fed with T. pyriformis was 3.3 ± 0.6 ciliate rot–1 h–1, i.e. 1.4 ± 0.3 ngC rot–1 h–1. Metazooplankton species for which the ingestion of ciliates could be measured were the rotifers Keratella cochlearis, Euchlanis dilatata and Synchaeta spp. Ingestion rates measured ranged from 0.4 to 12.5 ngC rot–1 h–1. The method proposed proved to be useful in estimating the predation of microplankton on ciliates in semi- in situ conditions; in further developments, labelled natural assemblages of ciliates could be used for in situ incubations with the Haney chamber.
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