The boundary layer of swimming fish

Citation
Ej. Anderson et al., The boundary layer of swimming fish, J EXP BIOL, 204(1), 2001, pp. 81-102
Citations number
54
Categorie Soggetti
Biology,"Experimental Biology
Journal title
JOURNAL OF EXPERIMENTAL BIOLOGY
ISSN journal
00220949 → ACNP
Volume
204
Issue
1
Year of publication
2001
Pages
81 - 102
Database
ISI
SICI code
0022-0949(200101)204:1<81:TBLOSF>2.0.ZU;2-0
Abstract
Tangential and normal velocity profiles of the boundary layer surrounding l ive swimming fish were determined by digital particle tracking velocimetry, DPTV. Two species were examined: the scup Stenotomus chrysops, a carangifo rm swimmer, and the smooth dogfish Mustelus canis, an anguilliform swimmer. Measurements were taken at several locations over the surfaces of the fish and throughout complete undulatory cycles of their propulsive motions. The Reynolds number based on length, Re, ranged from 3x10(3) to 3x10(5). In ge neral, boundary layer profiles were found to match known laminar and turbul ent profiles including those of Blasius, Falkner and Skan and the law of th e wall. In still water, boundary layer profile shape always suggested lamin ar flow. In flowing water, boundary layer profile shape suggested laminar f low at lower Reynolds numbers and turbulent flow at the highest Reynolds nu mbers. In some cases, oscillation between laminar and turbulent profile sha pes with body phase was observed. Local friction coefficients, boundary lay er thickness and fluid velocities at the edge of the boundary layer were su ggestive of local oscillatory and mean streamwise acceleration of the bound ary layer. The behavior of these variables differed significantly in the bo undary layer over a rigid fish. Total skin friction was determined. Swimmin g fish were found to experience greater friction drag than the same fish st retched straight in the flow. Nevertheless, the power necessary to overcome friction drag was determined to be within previous experimentally measured power outputs. No separation of the boundary layer was observed around swimming fish, sugg esting negligible form drag. Inflected boundary layers, suggestive of incip ient separation, were observed sporadically, but appeared to be stabilized at later phases of the undulatory cycle. These phenomena may be evidence of hydrodynamic sensing and response towards the optimization of swimming per formance.