Skip to main content
Log in

Metabolic cost of motility in planktonic protists: Theoretical considerations on size scaling and swimming speed

  • Published:
Microbial Ecology Aims and scope Submit manuscript

Abstract

The metabolic cost of swimming for planktonic protists is calculated, on theoretical grounds, from a simple model based upon Stokes' law. Energetic expenditure is scaled over both typically encountered size ranges (1–100 µm) and swimming speeds (100–5,000 µm/sec). In agreement with previous estimates for typical flagellates, these estimates generally suggest a low (<1%) cost for motility, related to total metabolic rate of growing cells. However, the cost of motility in small, fast-moving forms, such as some ciliates and flagellates, may be significant (1–10%) and even substantial (10–100%+) for certain species. In accordance with these predictions, many fast-moving ciliates restrict motility to bursts of activity or “jumps.” In the absence of a reduction in swimming speed or in the frequency of jumps, it is predicted that this relative cost of motility will be significantly increased in starving heterotrophs or light-limited autotrophs, if such cells reduce cell volumes and specific rates of respiration.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Bauerfeind E, Ellbrächter M, Steiner R, Throndsen J (1986) Application of Laser Doppler Spectroscopy (LDS) in determining swimming velocities of motile phytoplankton. Mar Biol 93:323–327

    Google Scholar 

  2. Crawford DW (1989) Mesodinium rubrum: The phytoplankter that wasn't. Mar Ecol Prog Ser 58:161–174

    Google Scholar 

  3. Crawford DW, Purdie DA (1992) Evidence for avoidance of flushing from an estuary by a planktonic phototrophic ciliate. Mar Ecol Prog Ser 79:259–265

    Google Scholar 

  4. Epp RW, Lewis WM (1984) Cost and speed of locomotion for rotifers. Oecologia (Berl) 61: 289–292

    Google Scholar 

  5. Dale T (1987) Diel vertical distribution of planktonic ciliates in Lindåspollene, Western Norway. Mar Microb Food Webs 2:15–28

    Google Scholar 

  6. Fauré-Fremiet E (1948) Le rhythme de marée du Strombidium oculatum Gruber. Bull Biol de France et de Belgique 82:3–23

    Google Scholar 

  7. Fenchel T, Finlay BJ (1983) Respiration rates in heterotrophic, free-living Protozoa. Microb Ecol 9:99–122

    Google Scholar 

  8. Horstmann U (1980) Observations on the peculiar diurnal migration of a red tide Dinophyceae in tropical shallow waters. J Phycol 16:481–485

    Google Scholar 

  9. Iriarte A, Daneri G, Garcia VMT, Purdie DA, Crawford DW (1991) Plankton community respiration and its relationship to chlorophyll a concentration in marine coastal waters. Oceanol Acta 14:379–387

    Google Scholar 

  10. Jonsson PR (1987) Photosynthetic assimilation of inorganic carbon in marine oligotrich ciliates (Ciliophora, Oligotrichina). Mar Microb Food Webs 2:55–68

    Google Scholar 

  11. Jonsson PR, Tiselius P (1990) Feeding behaviour, prey detection and capture efficiency of the copepod Acartia tonsa feeding on planktonic ciliates. Mar Ecol Prog Ser 60:35–44

    Google Scholar 

  12. Klekowski RZ (1981) Size dependence of metabolism in protozoans. Verh Internat Verein Limnol 21:1498–1502

    Google Scholar 

  13. Laval-Peuto M, Rassoulzadegan F (1988) Autofluorescence of marine planktonic Oligotrichina and other ciliates. Hydrobiologia 159:99–110

    Google Scholar 

  14. Levandosky M, Kaneta PJ (1987) Behaviour in dinoflagellates. In: Taylor FJR (ed) The biology of dinoflagellates. Botanical Monographs, vol 21. Blackwell Scientific Publications, Oxford, pp 360–397

    Google Scholar 

  15. Lindholm T (1981) On the ecology of Mesodinium rubrum (Lohmann) (Ciliata) in a stagnant brackish basin on Åland, SW Finland. Kiel Meeresforsch 5:117–123

    Google Scholar 

  16. Lindholm T (1985) Mesodinium rubrum—A unique photosynthetic ciliate. Adv Aquat Microbiol 3:1–48

    Google Scholar 

  17. Lombard EH, Capon B (1971) observations on the tidepool ecology and behaviour of Peridinium gregarium. J Phycol 7:188–194

    Google Scholar 

  18. Purcell EM (1977) Life at low Reynolds number. Am J Phys 45:3–11

    Google Scholar 

  19. Raven JA, Beardall J (1981) Respiration and photorespiration. Can Bull Fish Aquat Sci 210: 55–82

    Google Scholar 

  20. Raven JA, Richardson K (1984) Dinoflagellate flagella: A cost-benefit analysis. New Phytol 98:259–276

    Google Scholar 

  21. Roberts AM (1981) Hydrodynamics of protozoan swimming. In: Levandowsky M, Humer SH (eds) Biochemistry and physiology of protozoa. Academic Press, New York, pp 5–66

    Google Scholar 

  22. Sherr EB, Sherr BF, Paffenhöfer GA (1986) Phagotrophic protozoa as food for metazoans: A “missing” trophic link in marine pelagic food webs? Mar Microb Food Webs 1:61–80

    Google Scholar 

  23. Sleigh MA, Blake JR (1977) Methods of ciliary propulsion and their size limitations. In: Pedley TJ (ed) Scale effects in animal locomotion. Academic Press, New York, pp 243–256

    Google Scholar 

  24. Sorokin YI (1981) Microheterotrophic organisms in marine ecosystems. In: Longhurst AR (ed) Analysis of marine ecosystems. Academic Press, New York, pp 293–342

    Google Scholar 

  25. Sournia A (1982) Form and function in marine phytoplankton. Biol Rev 57:347–394

    Google Scholar 

  26. Stoecker DK, Michaels AE, Davis LH (1987) Large proportion of marine planktonic ciliates found to contain functional chloroplasts. Nature (Lond) 326:790–792

    Google Scholar 

  27. Stoecker DK, Silver MW, Michaels AE, Davis LH (1988) Obligate mixotrophy in Laboea strobila, a ciliate which retains chloroplasts. Mar Biol 99:415–423

    Google Scholar 

  28. Stoecker DK, Taniguchi A, Michaels AE (1989) Abundance of autotrophic, mixotrophic and heterotrophic planktonic ciliates in shelf and slope waters. Mar Ecol Prog Ser 50:241–254

    Google Scholar 

  29. Strickler JR (1974) Swimming of planktonic Cyclops species (Copepoda, Crustacca): Pattern, movements and their control. In: Wu TY, Brokaw CJ, Brennen C (eds) Swimming and flying in nature. Plenum Press, New York, pp 599–613

    Google Scholar 

  30. Tamar H (1979) The movements of jumping ciliates. Archiv für Protistenk 122:290–327

    Google Scholar 

  31. Throndsen J (1973) Motility in some marine nanoplankton flagellates. Norw J Zool 21:193–200

    Google Scholar 

  32. Vlymen WJ (1970) Energy expenditure of swimming in copepods. Limnol Oceanogr 15:348–356

    Google Scholar 

  33. Wu TY (1977) Introduction to the scaling of aquatic animal locomotion. In: Pedley TJ (ed) Scale effects in animal locomotion. Academic Press, New York, pp 203–232

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Crawford, D.W. Metabolic cost of motility in planktonic protists: Theoretical considerations on size scaling and swimming speed. Microb Ecol 24, 1–10 (1992). https://doi.org/10.1007/BF00171966

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00171966

Keywords

Navigation