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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INTRODUCTION<br />
within the microzooplankton, have rarely been investigated. In addition, experiments on<br />
microzooplankton are hampered by the fragility <strong>of</strong> certain groups (Gifford, 1985). The<br />
methodological approaches for the investigation <strong>of</strong> these species have to be improved as<br />
the conservation <strong>of</strong> fragile species for <strong>and</strong> also in experiments is fundamental to the<br />
ability to answer questions about their ecology.<br />
These examples, proxies for a whole list <strong>of</strong> unanswered questions, show that there is<br />
still a great need for further research on microzooplankton <strong>and</strong> its role in the marine<br />
food web. In the following paragraphs I will focus on the current knowledge on<br />
din<strong>of</strong>lagellates <strong>and</strong> ciliates to give a brief insight into their ecology.<br />
The most important microzooplankton groups: Din<strong>of</strong>lagellates <strong>and</strong> ciliates<br />
Din<strong>of</strong>lagellates <strong>and</strong> ciliates are cosmopolitan groups in marine, freshwater, benthic <strong>and</strong><br />
planktonic habitats. In the oceans they occur in such contrasting ecosystems as the<br />
eutrophic, turbid <strong>and</strong> shallow Wadden Sea, the oligotrophic tropical Pacific, the<br />
Mediterranean <strong>and</strong> the Polar Regions. Many species <strong>of</strong> both groups are known to be<br />
mixotrophic <strong>and</strong> their nutrition ranges from phototrophic with the ability to ingest<br />
organic particles, to phagotrophic with the additional ability to retain chloroplasts <strong>of</strong><br />
their prey organisms (so-called ‘kleptochloroplasts’) <strong>and</strong> to use these for<br />
photosynthesis. Examples <strong>of</strong> mixotrophy among phototrophic species are the ciliate<br />
Myrionecta rubra (Johnson & Stoecker, 2005) <strong>and</strong> a variety <strong>of</strong> phototrophic<br />
din<strong>of</strong>lagellates (Du Yoo et al., 2009); phagotrophs with the ability to retain chloroplasts<br />
are, e.g., the ciliate Laboea strobila (Stoecker et al., 1988) <strong>and</strong> the din<strong>of</strong>lagellate genus<br />
Dinophysis (Carvalho et al., 2008). However, many species in both groups display a<br />
purely heterotrophic nutrition.<br />
Din<strong>of</strong>lagellates<br />
Din<strong>of</strong>lagellates span a large size range from 2 µm (Gymnodinium simplex) to 2 mm<br />
(Noctiluca scintillans) (Taylor, 1987), but the size <strong>of</strong> the majority lies within 20 to 200<br />
µm thus belonging to the microzooplankton (Sieburth et al., 1978).<br />
Today approximately 2500 living species <strong>of</strong> various morphologically highly variable<br />
genera <strong>of</strong> din<strong>of</strong>lagellates have been described, <strong>of</strong> which roughly 40 – 60% are<br />
photosynthetic. However, among those din<strong>of</strong>lagellates regarded as photosynthetic a<br />
growing number is found to be capable <strong>of</strong> taking up organic carbon (mixotrophy) <strong>and</strong> <strong>of</strong><br />
active feeding (Du Yoo et al., 2009) (in this thesis the terms “din<strong>of</strong>lagellates” <strong>and</strong><br />
“heterotrophic din<strong>of</strong>lagellates” refer to the same: Species capable <strong>of</strong> active feeding).<br />
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