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School of Engineering and Science - Jacobs University

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CHAPTER IV<br />

feeding rates <strong>of</strong> F. ehrenbergii have been shown to be inhibited by a number <strong>of</strong><br />

dissolved free amino acids (Strom et al., 2007b) which could theoretically also be<br />

released by G. dominans. However, in our work growth rates <strong>of</strong> the tintinnid in the<br />

presence <strong>of</strong> the smaller predator were the same as when preying on S. trochoidea alone<br />

<strong>and</strong> thus such a chemical influence could be rejected.<br />

A different picture was observed in the last experiment with a new F. ehrenbergii<br />

culture. Here we detected a mortality rate <strong>of</strong> around -0.22 d -1 in the presence <strong>of</strong> F.<br />

ehrenbergii indicating predation on the smaller G. dominans. However, a pronounced<br />

selective predation on G. dominans that would also promote the autotrophic prey S.<br />

trochoidea due to the partial release <strong>of</strong> grazing pressure (Stoecker & Evans, 1985) was<br />

not observed in our experiments.<br />

Competitive predator relationship with a commensalistic element<br />

Our findings are in contrast to results <strong>of</strong> another study where no difference in growth<br />

rates was found for a din<strong>of</strong>lagellate or its potential ciliate predator competing for the<br />

same prey when compared to the single predator treatments (Jakobsen & Hansen, 1997)<br />

<strong>and</strong> another study where intraguild predation between the predators favoured the prey<br />

(Stoecker & Evans, 1985). Even if both predators competed for the same prey organism<br />

in our experiments G. dominans was directly supported by the presence, especially by<br />

the feeding, <strong>of</strong> the other predator leading to a higher efficiency in resource exploitation.<br />

This observed paradox could only be solved when looking at the feeding behaviour <strong>of</strong><br />

F. ehrenbergii. The din<strong>of</strong>lagellate directly benefited from immobilised but not ingested<br />

prey cells <strong>of</strong> the tintinnid. Benefits from “pre-conditioned prey” have been reported for<br />

din<strong>of</strong>lagellates before, e.g. when feeding on faecal pellets <strong>of</strong> copepods (Poulsen &<br />

Iversen, 2008).<br />

Although G. dominans can feed on different planktonic prey in the laboratory<br />

(Nakamura et al., 1995a) it is <strong>of</strong>ten highly abundant during red tides <strong>of</strong> mobile<br />

din<strong>of</strong>lagellate prey (Nakamura et al., 1995b, Kim & Jeong, 2004). Interestingly, G.<br />

dominans selected strongly for immobilised din<strong>of</strong>lagellates in our experiments even if<br />

mobile prey was available in the same concentration. This is most probably related to<br />

the feeding habit <strong>of</strong> G. dominans. Gyrodinium species display a smooth pre-capture<br />

swimming behaviour around the prey before it is captured <strong>and</strong> ingested (Hansen, 1992).<br />

Taking this habit <strong>and</strong> the swimming speed <strong>of</strong> the prey organism S. trochoidea into<br />

account it is clear that immobile prey cells are easier captured by G. dominans even if<br />

there were higher encounter rates with swimming prey (Gerritsen & Strickler, 1977).<br />

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