|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Journal of Experimental Biology, Vol 192, Issue 1 299-305, Copyright © 1994 by Company of Biologists
JOURNAL ARTICLES |
R Wilson and S Egginton
Levels of swimming activity in fishes have been divided into three categories on the basis of the time a given speed can be maintained before the onset of fatigue (Beamish, 1978): sustained (more than 200 min), prolonged (20 s to 200 min) and burst swimming (less than 20 s). The locomotory capacity of a given species reflects both its lifestyle and its body form, although definitions of performance may vary. It is generally accepted that only the aerobic ('red') muscle fibres should be active at truly sustainable swimming speeds, i.e. at speeds that can be maintained indefinitely without fatigue. However, the standard laboratory method of evaluating the maximum sustainable swimming speed (Ucrit; Brett, 1964) almost certainly entails the recruitment of at least some of the rapidly fatigable fast glycolytic ('white') fibres at sub-critical speeds and undoubtedly complicates the evaluation of maximal cardiovascular performance. It would therefore be useful to have an objective and reproducible measure of truly sustainable performance that, by definition, relies solely on aerobic muscle activity. Electromyography (EMG) has been used to examine the pattern of white muscle recruitment following thermal acclimation in striped bass, Morine saxatilis (Sisson and Sidell, 1987). We wished to incorporate this method into a study of the acclimatory responses to chronic changes in environmental temperature of the cardiovascular and locomotory systems in rainbow trout (Wilson and Egginton, 1992). The present communication presents results on the cardiovascular performance and blood chemistry, at rest and during maximal aerobic exercise, of rainbow trout acclimated to 11 °C, as a validation of the methodology currently in use with fish acclimated to seasonal temperature extremes (Taylor et al. 1992). Different acclimation temperatures are known to produce compensatory changes in the relative proportions of red and white muscle mass (Sidell and Moerland, 1989). The aim of these continuing investigations is to compare the anatomical, cardiovascular and locomotory limitations to aerobic exercise over the full temperature range of a eurythermal fish species.
This article has been cited by other articles:
![]() |
K. Anttila, S. Manttari, and M. Jarvilehto Effects of different training protocols on Ca2+ handling and oxidative capacity in skeletal muscle of Atlantic salmon (Salmo salar L.) J. Exp. Biol., August 1, 2006; 209(15): 2971 - 2978. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. L. Marsh and D. J. Ellerby Partitioning locomotor energy use among and within muscles Muscle blood flow as a measure of muscle oxygen consumption J. Exp. Biol., July 1, 2006; 209(13): 2385 - 2394. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. J. Peake and A. P. Farrell Locomotory behaviour and post-exercise physiology in relation to swimming speed, gait transition and metabolism in free-swimming smallmouth bass (Micropterus dolomieu) J. Exp. Biol., April 1, 2004; 207(9): 1563 - 1575. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. G. Drucker and G. V. Lauder Function of pectoral fins in rainbow trout: behavioral repertoire and hydrodynamic forces J. Exp. Biol., March 1, 2003; 206(5): 813 - 826. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. G. Richards, A. J. Mercado, C. A. Clayton, G. J. F. Heigenhauser, and C. M. Wood Substrate utilization during graded aerobic exercise in rainbow trout J. Exp. Biol., July 15, 2002; 205(14): 2067 - 2077. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Milligan, G. Hooke, and C Johnson Sustained swimming at low velocity following a bout of exhaustive exercise enhances metabolic recovery in rainbow trout J. Exp. Biol., January 3, 2000; 203(5): 921 - 926. [Abstract] [PDF] |
||||