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Journal of Experimental Biology, Vol 203, Issue 2 193-206, Copyright © 2000 by Company of Biologists
JOURNAL ARTICLES |
UK Muller, EJ Stamhuis and JJ Videler
Department of Marine Biology, University of Groningen, The Netherlands. ukm20@cam.ac.uk
Zebra danios (Brachydanio rerio) swim in a burst-and-coast mode. Most swimming bouts consist of a single tail flick and a coasting phase, during which the fish keeps its body straight. When visualising the flow in a horizontal section through the wake, the effects of the flow regime become apparent in the structure of the wake. In a two-dimensional, medio-frontal view of the flow, larvae and adults shed two vortices at the tail during the burst phase. These vortices resemble a cross section through a large-core vortex ring: two vortex cores packed close together with the central flow directed away from the fish. This flow pattern can be observed in larvae (body length approximately 4 mm) at Reynolds numbers below 100 as well as in adult fish (body length approximately 35 mm) at Reynolds numbers above 1000. Larval vortices differ from those of adult zebra danios mainly in their relatively wider vortex cores (higher ratio of core radius to ring radius) and their lower vortex circulation. Both effects result from the increased importance of viscosity on larval flows. During the coasting phase, larval and adult flows again differ because of the changing importance of viscosity. The high viscosity of the water causes large vortical flows adjacent to the larva's body. These regions of high vorticity represent the huge body of water dragged along by the larva, and they cause the larva to stop almost immediately after thrust generation ceases. No such areas of high vorticity are visible adjacent to adult zebra danios performing a comparable swimming manoeuvre. The rapid decrease in vortex circulation and the severe reduction in the coasting distance due to viscous drag contribute to the high cost that larvae - unlike adult fish - face when using a burst-and-coast swimming style.
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