Abstract
A general Boundary Element Method is presented and benchmarked with existing Slender Body Theory results and reflection solutions for the motion of spheres and slender bodies near plane boundaries. This method is used to model the swimming of a microorganism with a spherical cell body, propelled by a single rotating flagellum. The swimming of such an organism near a plane boundary, midway between two plane boundaries or in the vicinity of another similar organism, is investigated. It is found that only a small increase (less than 10%) results in the mean swimming speed of an organism swimming near and parallel to another identical organism. Similarly, only a minor propulsive advantage (again, less than 10% increase in mean swimming speed) is predicted when an organism swims very close and parallel to plane boundaries (such as a microscopic plate and (or) a coverslip, for example). This is explained in terms of the flagellar propulsive advantage derived from an increase in the ratio of the normal to tangential resistance coefficients of a slender body being offset by the apparently equally significant increase in the cell body drag. For an organism swimming normal to and toward a plane boundary, however, it is predicted that (assuming it is rotating its flagellum, relative to its cell body, with a constant angular frequency) the resulting swimming speed decreases asymptotically as the organism approaches the boundary.
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Selected References
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- Berg H. C., Anderson R. A. Bacteria swim by rotating their flagellar filaments. Nature. 1973 Oct 19;245(5425):380–382. doi: 10.1038/245380a0. [DOI] [PubMed] [Google Scholar]
- Berg H. C., Turner L. Chemotaxis of bacteria in glass capillary arrays. Escherichia coli, motility, microchannel plate, and light scattering. Biophys J. 1990 Oct;58(4):919–930. doi: 10.1016/S0006-3495(90)82436-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chwang A. T., Wu T. Y. A note on the helical movement of micro-organisms. Proc R Soc Lond B Biol Sci. 1971 Aug 3;178(1052):327–346. doi: 10.1098/rspb.1971.0068. [DOI] [PubMed] [Google Scholar]
- Gueron S., Liron N. Ciliary motion modeling, and dynamic multicilia interactions. Biophys J. 1992 Oct;63(4):1045–1058. doi: 10.1016/S0006-3495(92)81683-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Keller J. B., Rubinow S. I. Swimming of flagellated microorganisms. Biophys J. 1976 Feb;16(2 Pt 1):151–170. doi: 10.1016/s0006-3495(76)85672-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meister M., Caplan S. R., Berg H. C. Dynamics of a tightly coupled mechanism for flagellar rotation. Bacterial motility, chemiosmotic coupling, protonmotive force. Biophys J. 1989 May;55(5):905–914. doi: 10.1016/S0006-3495(89)82889-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Myerscough M. R., Swan M. A. A model for swimming unipolar spirilla. J Theor Biol. 1989 Jul 21;139(2):201–218. doi: 10.1016/s0022-5193(89)80100-6. [DOI] [PubMed] [Google Scholar]
- Ramia M. Numerical model for the locomotion of spirilla. Biophys J. 1991 Nov;60(5):1057–1078. doi: 10.1016/S0006-3495(91)82143-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rikmenspoel R. The tail movement of bull spermatozoa. Observations and model calculations. Biophys J. 1965 Jul;5(4):365–392. doi: 10.1016/S0006-3495(65)86723-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schreiner K. E. The helix as propeller of microorganisms. J Biomech. 1971 Jan;4(1):73–83. doi: 10.1016/0021-9290(71)90017-0. [DOI] [PubMed] [Google Scholar]
- Sleigh M. A., Blake J. R., Liron N. The propulsion of mucus by cilia. Am Rev Respir Dis. 1988 Mar;137(3):726–741. doi: 10.1164/ajrccm/137.3.726. [DOI] [PubMed] [Google Scholar]
- Swan M. A. Trailing flagella rotate faster than leading flagella in unipolar cells of Spirillum volutans. J Bacteriol. 1982 Apr;150(1):377–380. doi: 10.1128/jb.150.1.377-380.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]