An emerging consensus from studies of axial and limb networks is that different premotor populations are required for different speeds of locomotion. An important but unresolved issue is why this occurs. Here, we perform voltage-clamp recordings from axial motoneurons in larval zebrafish during "fictive" swimming to test the idea that systematic differences in the biophysical properties of axia...

Because of the inherent inefficiency of jet propulsion, squid are considered to be at a competitive disadvantage compared with fishes, which generally depend on forms of undulatory/oscillatory locomotion. Some squid, such as the brief squid Lolliguncula brevis, swim at low speeds in shallow-water complex environments, relying heavily on fin activity. Consequently, their swimming costs may be lo...

Power represents the ability to perform movements at high speed, or the possibility of developing high strength in a short time. More than sixty years ago the relationship between power, strength and speed of muscle contraction was described by Hill [1]. Swimming performance is a multi-factorial phenomenon depending upon energetics, biomechanics, hydrodynamics, anthropometrics and strength para...

BACKGROUND The present study investigated the changes in swimming speeds and sex differences for elite male and female swimmers competing in 5 km, 10 km and 25 km open-water FINA World Cup races held between 2000 and 2012. METHODS The changes in swimming speeds and sex differences across years were analysed using linear, non-linear, and multi-level regression analyses for the annual fastest a...

When removed from their egg membranes, Xenopus embryos can swim. High-speed cinematography shows that, in swimming, lateral undulations pass rostro-caudally down the body. The swimming rhythm period is 40-100 ms. In swimming, electrical activity in myotomal muscles alternates on opposite sides of a segment and sweeps rostro-caudally in ipsilateral myotomes. Myotome muscle physiology was examine...

Rowing is demanding, in part, because drag on the oars increases as the square of their speed. Hence, as muscles shorten faster, their force capacity falls, whereas drag rises. How do frogs resolve this dilemma to swim rapidly? We predicted that shortening velocity cannot exceed a terminal velocity where muscle and fluid torques balance. This terminal velocity, which is below Vmax, depends on g...

Swim speed, dive behavior and movements were recorded for seven female leatherback sea turtles (Dermochelys coriacea Vandelli 1761) during a single internesting interval near St Croix in the US Virgin Islands. Modal speeds ranged from 0.56 to 0.84 m s(-1), maximum speed range 1.9-2.8 m s(-1). Turtles swam continuously throughout the day and night. There were two swim-speed patterns; the most co...

When a microorganism begins swimming from rest in a Newtonian fluid such as water, it rapidly attains its steady-state swimming speed since changes in the velocity field spread quickly when the Reynolds number is small. However, swimming microorganisms are commonly found or studied in complex fluids. Because these fluids have long relaxation times, the time to attain the steady-state swimming s...

Contrary to the previous premise that pelvic fins lacked obvious function, recent work on three-dimensional fin motions suggests that pelvic fins actively control stability and speed in slowly swimming trout. This study used electromyography to measure pelvic fin muscle activity and particle imaging velocimetry to quantify flow along the ventral body region to test this hypothesis. Fish swam at...

Microorganisms often encounter anisotropy, for example in mucus and biofilms. We study how anisotropy and elasticity of the ambient fluid affects the speed of a swimming microorganism with a prescribed stroke. Motivated by recent experiments on swimming bacteria in anisotropic environments, we extend a classical model for swimming microorganisms, the Taylor swimming sheet, actuated by small-amp...