Hatchling sea turtles emerge from nests, crawl down the beach and enter the sea where they typically enter a stereotypical hyperactive swimming frenzy. During this swim the front flippers are moved up and down in a flapping motion and are the primary source of thrust production. I used high-speed video linked with simultaneous measurement of thrust production in tethered hatchlings, along with ...

Approved for public release; distribution is unlimited. iv " The dolphins usually swim ahead of the ship, or sometimes alongside, but never in the ship's wake. Unlike sharks, which follow ocean liners for their refuse, dolphins merely come up to play, sometimes jumping right out of the water, darting across the bow waves and even diving under the ship. They are never covetous and never beg. On ...

Swimming performance is considered a key trait determining the ability of fish to survive. Hydrodynamic theory predicts that the energetic costs required for fishes to swim should vary with speed according to a U-shaped curve, with an expected energetic minimum at intermediate cruising speeds and increasing expenditure at low and high speeds. However, to date no complete datasets have shown an ...

A large swim tunnel respirometer was used to quantify the swimming energetics of the eastern Pacific bonito Sarda chiliensis (tribe Sardini) (45-50 cm fork length, FL) at speeds between 50 and 120 cm s(-1) and at 18+/-2 degrees C. The bonito rate of oxygen uptake ((O(2)))-speed function is U-shaped with a minimum (O(2)) at 60 cm s(-1), an exponential increase in (O(2)) with increased speed, and...

Squids use a pulsed jet and fin movements to swim both arms-first (forward) and tail-first (backward). Given the complexity of the squid multi-propulsor system, 3D velocimetry techniques are required for the comprehensive study of wake dynamics. Defocusing digital particle tracking velocimetry, a volumetric velocimetry technique, and high-speed videography were used to study arms-first and tail...

Pseudomonas aeruginosa is a monoflagellated bacterium that can use its single polar flagellum to swim through liquids and move collectively over semisolid surfaces, a behavior called swarming. Previous studies have shown that experimental evolution in swarming colonies leads to the selection of hyperswarming bacteria with multiple flagella. Here we show that the advantage of such hyperswarmer m...

It has long been suspected that the denticles on shark skin reduce hydrodynamic drag during locomotion, and a number of man-made materials have been produced that purport to use shark-skin-like surface roughness to reduce drag during swimming. But no studies to date have tested these claims of drag reduction under dynamic and controlled conditions in which the swimming speed and hydrodynamics o...

The effects of water temperature and ammonia concentration on swimming capacity of brook charr (Salvelinus fontinalis, Mitchill, 1814) were determined by measuring gait transition speed (U(gt), cms(-1)), maximum burst speed (U(max), cms(-1)), tail-beat amplitude (a, cm), tail-beat frequency (f, Hz), maximum acceleration of bursts (A(max), cms(-2)), number of bursts, distance of bursts (cm) and ...

Compromises between swimming and feeding affect larval form and behavior. Two hypotheses, with supporting examples, illustrate these feeding-swimming trade-offs. (1) Extension of ciliated bands into long loops increases maximum clearance rates in feeding but can decrease stability of swimming in shear flows. A hydromechanical model of swimming by ciliated bands on arms indicates that morphologi...

Arterial plasma K+ and lactate concentrations ([K+]a and [lactate]a), as well as blood oxygenation status, were measured in relation to increasing swimming speeds in rainbow trout Oncorhynchus mykiss. Neither [K+]a nor [lactate]a changed at swimming speeds below 1.5 BL s-1, where BL is total body length. Between 1.5 and 2.0 BL s-1, [K+]a started to increase, and above 2.0 BL s-1 both [K+]a and ...