PubMed Health⌕ Search

Biomedical subjects

D J Ellerby

Publications and source records attributed to D J Ellerby.

5 recordsLinked to original sources

Fast muscle function in the European eel (Anguilla anguilla L.) during aquatic and terrestrial locomotion.

Eels are capable of locomotion both in water and on land using undulations of the body axis. Axial undulations are powered by the lateral musculature. Differences in kinematics and the underlying patterns of fast muscle activation are apparent between locomotion in these two environments. The change in isometric fast muscle properties with axial location was less marked than in most other species. Time from stimulus to peak force (T(a)) did not change significantly with axial position and was 82+/-6 ms at 0.45BL and 93+/-3 ms at 0.75BL, where BL is total body length. Time from stimulus to 90% relaxation (T(90)) changed significantly with axial location, increasing from 203+/-11ms at 0.45BL to 239+/-9 ms at 0.75BL. Fast muscle power outputs were measured using the work loop technique. Maximum power outputs at +/-5% strain using optimal stimuli were 17.3+/-1.3W kg(-1) in muscle from 0.45BL and 16.3+/-1.5W kg(-1) in muscle from 0.75BL. Power output peaked at a cycle frequency of 2Hz. The stimulus patterns associated with swimming generated greater force and power than those associated with terrestrial crawling. This decrease in muscle performance in eels may occur because on land the eel is constrained to a particular kinematic pattern in order to produce thrust against an underlying substratum.

Anguilla↗

Spatial variation in fast muscle function of the rainbow trout Oncorhynchus mykiss during fast-starts and sprinting.

Fish fast-starts and sprints are rapid kinematic events powered by the lateral myotomal musculature. A distinction can be made between fast-starts and sprint-swimming activity. Fast-starts are kinematic events involving rapid, asymmetrical movements. Sprints involve a series of symmetrical, high-frequency tailbeats that are kinematically similar to lower-frequency, sustained swimming. The patterns of muscle recruitment and strain associated with these swimming behaviours were determined using electromyography and sonomicrometry. Axial patterns of fast muscle recruitment during sprints were similar to those in slow muscle in that the duration of electromyograhic (EMG) activity decreased in a rostro-caudal direction. There was also an axial shift in activity relative to the strain cycle so that activity occurred relatively earlier in the caudal region. This may result in caudal muscle performing a greater proportion of negative work and acting as a power transmitter as well as a power producer. The threshold tailbeat frequency for recruitment of fast muscle differed with location in the myotome. Superficial muscle fibres were recruited at lower tailbeat frequencies and shortening velocities than those deeper in the musculature. During sprints, fast muscle strain ranged from +/- 3.4% l(0) (where l(0) is muscle resting length) at 0.35FL (where FL is fork length) to +/- 6.3% l(0) at 0.65FL. Fast-starts involved a prestretch of up to 2.5% l(0) followed by shortening of up to 11.3% l(0). Stage 1 EMG activity began simultaneously, during muscle lengthening, at all axial locations. Stage 2 EMG activity associated with the major contralateral contraction also commenced during lengthening and proceeded along the body as a wave. Onset of muscle activity during lengthening may enhance muscle power output.

Animals↗

Slow muscle power output of yellow- and silver-phase European eels (Anguilla anguilla L.): changes in muscle performance prior to migration.

Eels swim in the anguilliform mode in which the majority of the body axis undulates to generate thrust. For this reason, muscle function has been hypothesised to be relatively uniform along the body axis relative to some other teleosts in which the caudal fin is the main site of thrust production. The European eel (Anguilla anguilla L.) has a complex life cycle involving a lengthy spawning migration. Prior to migration, there is a metamorphosis from a yellow (non-migratory) to a silver (migratory) life-history phase. The work loop technique was used to determine slow muscle power outputs in yellow- and silver-phase eels. Differences in muscle properties and power outputs were apparent between yellow- and silver-phase eels. The mass-specific power output of silver-phase slow muscle was greater than that of yellow-phase slow muscle. Maximum slow muscle power outputs under approximated in vivo conditions were 0.24 W kg(-1) in yellow-phase eel and 0.74 W kg(-1) in silver-phase eel. Power output peaked at cycle frequencies of 0.3--0.5 Hz in yellow-phase slow muscle and at 0.5--0.8 Hz in silver-phase slow muscle. The time from stimulus offset to 90 % relaxation was significantly greater in yellow- than in silver-phase eels. The time from stimulus onset to peak force was not significantly different between life-history stages or axial locations. Yellow-phase eels shifted to intermittent bursts of higher-frequency tailbeats at a lower swimming speed than silver-phase eels. This may indicate recruitment of fast muscle at low speeds in yellow-phase eels to compensate for a relatively lower slow muscle power output and operating frequency.

Animals↗

Slow muscle function of Pacific bonito (Sarda chiliensis) during steady swimming.

The Pacific bonito, Sarda chiliensis, is anatomically intermediate between mackerel and tuna. The specialisations exhibited by tuna are present in the bonito, but to a lesser degree. Slow-twitch muscle strain and activity patterns were determined during steady swimming (tailbeat frequency 1.2-3.2 Hz) at four locations on the body of Sarda chiliensis using sonomicrometry and electromyography. Both strain and the phase of electromygraphic activity were independent of tailbeat frequency. The strain of superficial slow-twitch muscle increased from +/-3.1 % l(0) at 0.35FL to +/-5.8 % l(0) at 0.65FL, where l(0) is muscle resting length and FL is the body length from snout to tail fork. Between 0.35 and 0.65FL, there was a negative phase shift of 16 degrees in the onset of electromygraphic activity in superficial slow-twitch muscle relative to the strain cycle. Muscle activity patterns are comparable with those of tuna. At 0.58FL, the onset of activity in deep slow-twitch muscle was approximately synchronous with the onset of activity in superficial muscle in the same myotome at 0.65FL. The distribution of slow-twitch muscle along the body of Sarda chiliensis and four additional fish species, Anguilla anguilla, Oncorhynchus mykiss, Scomber scombrus and Thunnus albacares, was also measured. Slow-twitch muscle appears to become more concentrated at approximately 0.5FL as swimming kinematics become more thunniform.

Animals↗

Fish swimming: patterns in muscle function.

Undulatory swimming in fish is powered by the segmental body musculature of the myotomes. Power generated by this muscle and the interactions between the fish and the water generate a backward-travelling wave of lateral displacement of the body and caudal fin. The body and tail push against the water, generating forward thrust. The muscle activation and strain patterns that underlie body bending and thrust generation have been described for a number of species and show considerable variation. This suggests that muscle function may also vary among species. This variation must be due in large part to the complex interactions between muscle mechanical properties, fish body form, swimming mode, swimming speed and phylogenetic relationships. Recent work in several laboratories has been directed at studying patterns of muscle power output in vitro under simulated swimming conditions. This work suggests that the way that fish generate muscle power and convert it into thrust through the body and caudal fin does indeed vary. However, despite the differences, several features appear to be common to virtually all species studied and suggest where future effort should be directed if muscle function in swimming fish is to be better understood.

Animals↗