School of Engineering and Science - Jacobs University
School of Engineering and Science - Jacobs University
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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