A theoretical model describes how an intermittent swimming style can be energetically advantageous over continuous swimming at high average velocities. Kinematic data are collected from high-speed ciné pictures of free swimming cod and saithe at high velocities in a burst-and-coast style. These data suggest that fish make use of the advantages shown by choosing initial and final burst velocitie...

This paper presents simplified hydrodynamics model for a biomimetic robot fish based on quantitative morphological and kinematic parameters of crangiform fish. The motion of four Pangasius sanitwongsei with different length and swimming speed were recorded by the digital particle image velocimetry (DPIV) and image processing methods and optimal coefficients of the motion equations and appropria...

In this thesis, I present a detailed analysis of the role cell morphology, solution rheology, and swimming mechanism has on the motility of Helicobacter Pylori. H. Pylori, the bacterium that causes gastric ulcers, has a helical cell shape that has long been believed to provide an advantage in penetrating the viscous mucus layer protecting the stomach lining, its niche environment. I present res...

We investigate 3-dimensional flagellar swimming in a fluid with a sparse network of stationary obstacles or fibers. The Brinkman equation is used to model the average fluid flow where a flow dependent term, including a resistance parameter that is inversely proportional to the permeability, models the resistive effects of the fibers on the fluid. To solve for the local linear and angular veloci...

The purpose of this thesis is to study the problem when a microorganism swims very close to a shaped boundary. In this problem, we model the swimmer to be a two-dimensional, infinite periodic waving sheet. For simplicity, we only consider the case where the fluid between the swimmer and the washboard is Newtonian and incompressible. We assume that the swimmer propagates waves along its body and...

The aim of this study was to typify cardiorespiratory and metabolic adaptation capacity at race pace of high-level triathletes during simulations of short distance triathlon swimming sector, first transition and cycling sector. Six national and international-level triathletes performed a 1500 m swimming trial followed by a transition and one hour on ergocycle at race pace, with sequenced measur...

The spontaneous swimming activity of Atlantic cod Gadus morhua was investigated at graded levels of hypoxia at three temperatures (5, 10 and 15 °C) by using a computerized system monitoring animal activity. The fish were tested individually, and swimming distance was used as a measure of activity. No significant effect of temperature on swimming distance in normoxic water was found. At all ...

(1) The standard oxygen consumption and the oxygen consumption during measured swimming activity have been determined in three flatfish species at 5, 10 and 15 degrees C. (2) The relationship between weight and standard oxygen consumption for flatfish conform to the general relationship Y = aWb. On an interspecies basis, standard oxygen consumption of flatfish is significantly lower than that o...

We study magnetic artificial flagella whose swimming speed and direction can be controlled using light and magnetic field as external triggers. The dependence of the swimming velocity on the system parameters (e.g., length, stiffness, fluid viscosity, and magnetic field) is explored using a computational framework in which the magnetostatic, fluid dynamic, and solid mechanics equations are solv...

been describ neurons and neuromuscu 1989b; Satte Spencer, 1985; Satterlie et al. 1985, 1990). The pattern generator is relatively simple, producing a two-phase output that is translated into dorsal and ventral flexions of a pair of wing-like parapodia. Two forms of swimming, slow and fast, have been described which reflect plasticity in the organization of the pattern generator since the change...