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 Duthie, G.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Duthie, G.

Journal of Experimental Biology, Vol 97, Issue 1 359-373, Copyright © 1982 by Company of Biologists


JOURNAL ARTICLES

The respiratory metabolism of temperature-adapted flatfish at rest and during swimming activity and the use of anaerobic metabolism at moderate swimming speeds

GG Duthie

(1) The standard oxygen consumption and the oxygen consumption during measured swimming activity have been determined in three flatfish species at 5, 10 and 15 degrees C. (2) The relationship between weight and standard oxygen consumption for flatfish conform to the general relationship Y = aWb. On an interspecies basis, standard oxygen consumption of flatfish is significantly lower than that of roundfish. (3) A semilogarithmic model describes the relationship between oxygen consumption and swimming speed for the three species. Values for maximum oxygen consumption, metabolic scopes and critical swimming speeds are low in comparison to salmonids. (4) The optimum swimming speeds and critical swimming speeds of flatfish are similar. It is suggested that, over long distances, flatfish adopt a strategy of swimming at supercritical speeds with periods of intermittent rest to repay the accrued oxygen debt. (5) Elevated lactic acid levels in flounder white muscle after moderate swimming indicate an additional 15% anaerobic contribution to the cost of locomotion as calculated from aerobic considerations.


This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
P. C. Mendonca, A. G. Genge, E. J. Deitch, and A. K. Gamperl
Mechanisms responsible for the enhanced pumping capacity of the in situ winter flounder heart (Pseudopleuronectes americanus)
Am J Physiol Regulatory Integrative Comp Physiol, November 1, 2007; 293(5): R2112 - R2119.
[Abstract] [Full Text] [PDF]


Home page
ICES J. Mar. Sci.Home page
R. Kawabe, Y. Naito, K. Sato, K. Miyashita, and N. Yamashita
Direct measurement of the swimming speed, tailbeat, and body angle of Japanese flounder (Paralichthys olivaceus)
ICES J. Mar. Sci., January 1, 2004; 61(7): 1080 - 1087.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
P. W. Webb
Kinematics of plaice, Pleuronectes platessa, and cod, Gadus morhua, swimming near the bottom
J. Exp. Biol., July 15, 2002; 205(14): 2125 - 2134.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
I. K. Bartol, R. Mann, and M. R. Patterson
Aerobic respiratory costs of swimming in the negatively buoyant brief squid Lolliguncula brevis
J. Exp. Biol., January 11, 2001; 204(21): 3639 - 3653.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1982