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 />
the same patterns in G. dominans in a three-species treatment as was found in the first<br />
experiment. Bottles containing only S. trochoidea <strong>and</strong> G. dominans served as controls.<br />
We also monitored the effect <strong>of</strong> the direct presence <strong>of</strong> the larger predator on swimming<br />
behaviour <strong>and</strong> speed <strong>of</strong> S. trochoidea <strong>and</strong> G. dominans after exposure to F. ehrenbergii<br />
for 24 hours. Fixation for cell counts with acid Lugol’s solution took place before <strong>and</strong><br />
immediately after the time <strong>of</strong> incubation <strong>and</strong> filming.<br />
Counting<br />
Samples were enumerated under a Zeiss Axiovert 135 inverted microscope using the<br />
Utermöhl method (Utermöhl, 1958). The samples were settled overnight <strong>and</strong> 4-6<br />
circular transects <strong>of</strong> each settling chamber were counted at 200 or 400-fold<br />
magnification depending on cell concentration <strong>of</strong> S. trochoidea <strong>and</strong> G. dominans. For F.<br />
ehrenbergii the whole chamber was enumerated. Apart from the first experiment G.<br />
dominans cells containing fresh food vacuoles (indicated by the dark colour <strong>of</strong> the<br />
vacuoles) were recorded separately <strong>and</strong> food vacuoles were used as a proxy for<br />
ingestion.<br />
Calculations<br />
Growth <strong>and</strong> grazing parameters<br />
Growth rates k [d -1 ] <strong>of</strong> F. ehrenbergii, G. dominans <strong>and</strong> S. trochoidea in the<br />
experiments were calculated assuming exponential growth. Grazing rates g [d -1 ],<br />
specific filtration rates F [mL µg predator -1 d -1 ] <strong>and</strong> specific ingestion rates I [prey cells<br />
predator -1 d -1 ] <strong>of</strong> the predators were calculated according to Frost (1972) with the<br />
modification <strong>of</strong> Heinbokel (1978a) for the growth <strong>of</strong> predators. Predator biomass<br />
specific ingestion rates I b [µg prey µg predator -1 d -1 ] were calculated to allow for<br />
comparisons between the treatments by normalization <strong>of</strong> the specific ingestion rates to<br />
mean predator <strong>and</strong> prey biomass. Growth <strong>of</strong> phytoplankton is known to be density<br />
dependent. The S. trochoidea growth control in the general interaction experiment<br />
significantly exceeded the initial start concentrations after 24 <strong>and</strong> 48 hours <strong>of</strong><br />
incubation. In contrast, the initial concentrations <strong>of</strong> S. trochoidea in the grazing<br />
treatments at these times were close to starting concentrations <strong>of</strong> the first day. We<br />
therefore always used the growth rate <strong>of</strong> S. trochoidea determined after the first day for<br />
our calculations in the general interaction experiment.<br />
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