spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Feldkamp, S.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Feldkamp, S.

Journal of Experimental Biology, Vol 131, Issue 1 117-135, Copyright © 1987 by Company of Biologists


JOURNAL ARTICLES

Swimming in the California sea lion: morphometrics, drag and energetics

SD Feldkamp
Physiological Research Laboratory, Scripps Institution of Oceanography, La Jolla, CA 92093.

During swimming, the California sea lion, Zalophus californianus (Lesson), generates thrust forces solely by means of its pectoral flippers. This study examines the drag, energetic cost and efficiency associated with this method of locomotion. Sea lions are highly streamlined, with a fineness ratio of 5.5 and maximum girth at 40% of body length. This profile leads to reduced drag and swimming power requirements. Films of gliding animals showed the drag coefficient (based on wetted surface area) to be 0.0042 at a Reynolds number of 2.0 X 10(6). This value is comparable to that found for other aquatic vertebrates and suggests that the sea lion's morphology helps to delay turbulent separation and maintain laminar flow over the forward portion of its body. Swimming metabolism was measured in a water flume at velocities up to 1.3 ms-1. Effective swimming speeds up to 2.7 ms-1 were attained by increasing each animal's drag. Oxygen consumption rose exponentially with velocity and for two animals was best described as VO2 = 6.27e0.48U, where VO2 is in mlO2 min-1 kg-1 and U is in ms-1. Minimum cost of transport for these animals was 0.12 ml O2 kg-1 m-1 at a relative speed of 1.4 body lengths s-1. This is 2.5 times that predicted for a fish of similar size. Swimming efficiencies were determined from these results using power output values calculated from the measured drag coefficient and standard hydrodynamic equations. At the highest velocity, aerobic efficiency reached a maximum of 15% while mechanical efficiency of the foreflippers was 80%. The results demonstrate that foreflipper propulsion is a highly efficient and comparatively inexpensive method of locomotion in aquatic mammals.


This article has been cited by other articles:


Home page
Integr. Comp. Biol.Home page
F. E. Fish, L. E. Howle, and M. M. Murray
Hydrodynamic flow control in marine mammals
Integr. Comp. Biol., May 6, 2008; (2008) icn029v1.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
S. L. Gallon, C. E. Sparling, J.-Y. Georges, M. A. Fedak, M. Biuw, and D. Thompson
How fast does a seal swim? Variations in swimming behaviour under differing foraging conditions
J. Exp. Biol., September 15, 2007; 210(18): 3285 - 3294.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
M. J. Weise and D. P. Costa
Total body oxygen stores and physiological diving capacity of California sea lions as a function of sex and age
J. Exp. Biol., January 15, 2007; 210(2): 278 - 289.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
Y. Watanabe, E. A. Baranov, K. Sato, Y. Naito, and N. Miyazaki
Body density affects stroke patterns in Baikal seals
J. Exp. Biol., September 1, 2006; 209(17): 3269 - 3280.
[Abstract] [Full Text] [PDF]


Home page
PaleobiologyHome page
F. R. O'Keefe and M. T. Carrano
Correlated trends in the evolution of the plesiosaur locomotor system
Paleobiology, December 1, 2005; 31(4): 656 - 675.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
P. J. O. Miller, M. P. Johnson, P. L. Tyack, and E. A. Terray
Swimming gaits, passive drag and buoyancy of diving sperm whales Physeter macrocephalus
J. Exp. Biol., May 1, 2004; 207(11): 1953 - 1967.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
J Lovvorn, G. Liggins, M. Borstad, S. Calisal, and J Mikkelsen
Hydrodynamic drag of diving birds: effects of body size, body shape and feathers at steady speeds
J. Exp. Biol., May 1, 2001; 204(9): 1547 - 1557.
[Abstract] [PDF]


Home page
Integr. Comp. Biol.Home page
T. M. Williams
Intermittent Swimming by Mammals: A Strategy for Increasing Energetic Efficiency During Diving
Integr. Comp. Biol., April 1, 2001; 41(2): 166 - 176.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
J. A. Hurley and D. P. Costa
Standard metabolic rate at the surface and during trained submersions in adult California sea lions (Zalophus californianus)
J. Exp. Biol., January 10, 2001; 204(19): 3273 - 3281.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
L. Stelle, R. Blake, and A. Trites
Hydrodynamic drag in steller sea lions (Eumetopias jubatus)
J. Exp. Biol., January 6, 2000; 203(12): 1915 - 1923.
[Abstract] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
I. L. Boyd, R. M. Bevan, A. J. Woakes, and P. J. Butler
Heart rate and behavior of fur seals: implications for measurement of field energetics
Am J Physiol Heart Circ Physiol, March 1, 1999; 276(3): H844 - H857.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
F. Fish and R. Baudinette
Energetics of locomotion by the Australian water rat (Hydromys chrysogaster): a comparison of swimming and running in a semi-aquatic mammal
J. Exp. Biol., January 2, 1999; 202(4): 353 - 363.
[Abstract] [PDF]




© The Company of Biologists Ltd 1987