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 Figures Only
Right arrow Full Text
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 Similar articles in PubMed
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 Bernal, D.
Right arrow Articles by Graham, J. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bernal, D.
Right arrow Articles by Graham, J. B.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?
The Journal of Experimental Biology 204, 4043-4054 (2001)
© 2001 The Company of Biologists Limited

Water-tunnel studies of heat balance in swimming mako sharks

Diego Bernal*, Chugey Sepulveda and Jeffrey B. Graham

Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA 92093-0204, USA

*e-mail: dbernal{at}ucsd.edu

Accepted September 24, 2001

The mako shark (Isurus oxyrinchus) has specialized vascular networks (retia mirabilia) forming counter-current heat exchangers that allow metabolic heat retention in certain regions of the body, including the aerobic, locomotor red muscle and the viscera. Red muscle, white muscle and stomach temperatures were measured in juvenile (5–13.6 kg) makos swimming steadily in a water tunnel and exposed to stepwise square-wave changes in ambient temperature (Ta) to estimate the rates of heat transfer and to determine their capacity for the activity-independent control of heat balance. The rates of heat gain of red muscle during warming were significantly higher than the rates of heat loss during cooling, and neither the magnitude of the change in Ta nor the direction of change in Ta had a significant effect on red muscle latency time. Our findings for mako red muscle are similar to those recorded for tunas and suggest modulation of retial heat-exchange efficiency as the underlying mechanism controlling heat balance. However, the red muscle temperatures measured in swimming makos (0.3–3°C above Ta) are cooler than those measured previously in larger decked makos. Also, the finding of non-stable stomach temperatures contrasts with the predicted independence from Ta recorded in telemetry studies of mako and white sharks. Our studies on live makos provide new evidence that, in addition to the unique convergent morphological properties between makos and tunas, there is a strong functional similarity in the mechanisms used to regulate heat transfer.

Key words: lamnid, shark, Isurus oxyrinchus, tuna, thermoregulation, endothermy, red muscle, white muscle, stomach, heat balance, water tunnel.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
J. M. Donley, R. E. Shadwick, C. A. Sepulveda, and D. A. Syme
Thermal dependence of contractile properties of the aerobic locomotor muscle in the leopard shark and shortfin mako shark
J. Exp. Biol., April 1, 2007; 210(7): 1194 - 1203.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
C. A. Duong, C. A. Sepulveda, J. B. Graham, and K. A. Dickson
Mitochondrial proton leak rates in the slow, oxidative myotomal muscle and liver of the endothermic shortfin mako shark (Isurus oxyrinchus) and the ectothermic blue shark (Prionace glauca) and leopard shark (Triakis semifasciata)
J. Exp. Biol., July 15, 2006; 209(14): 2678 - 2685.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
C. A. Sepulveda, N. C. Wegner, D. Bernal, and J. B. Graham
The red muscle morphology of the thresher sharks (family Alopiidae)
J. Exp. Biol., November 15, 2005; 208(22): 4255 - 4261.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
C. A. Sepulveda, K. A. Dickson, and J. B. Graham
Swimming performance studies on the eastern Pacific bonito Sarda chiliensis, a close relative of the tunas (family Scombridae) I. Energetics
J. Exp. Biol., August 15, 2003; 206(16): 2739 - 2748.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
D. Bernal, C. Sepulveda, O. Mathieu-Costello, and J. B. Graham
Comparative studies of high performance swimming in sharks I. Red muscle morphometrics, vascularization and ultrastructure
J. Exp. Biol., August 15, 2003; 206(16): 2831 - 2843.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
D. Bernal, D. Smith, G. Lopez, D. Weitz, T. Grimminger, K. Dickson, and J. B. Graham
Comparative studies of high performance swimming in sharks II. Metabolic biochemistry of locomotor and myocardial muscle in endothermic and ectothermic sharks
J. Exp. Biol., August 15, 2003; 206(16): 2845 - 2857.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2001