Abstract:Locomotion is energetically expensive. This may create selection pressures that favor economical locomotor strategies, such as the adoption of low-cost speeds and efficient propulsive movements. For swimming fish, the energy expended to travel a unit distance, or cost of transport (COT), has a U-shaped relationship to speed. The relationship between propulsive kinematics and speed, summarized by the Strouhal number (St=fA/U, where f is tail beat frequency, A is tail tip amplitude in m and U is swimming speed i… Show more
“…This stems in part from the scarcity of data for unconstrained, volitional swimming. The combined availability of large-volume calibration techniques recently applied to quantify avian flight performance in the field [11] and low-cost underwater cameras has enabled the collection of field performance data for fish [5,12] with higher temporal and spatial resolution than has previously been possible [1]. This approach has revealed the use of intermittent propulsion during routine, sustained locomotion at aerobically sustained speeds and propulsive cycle frequencies, but with insufficient detail to indicate why this swimming style is used [5].…”
Bluegill sunfish use intermittent propulsion during volitional swimming. The function of this propulsive mode during routine swimming has not been well quantified. At low speeds, propulsive cycle frequencies and amplitudes were constant, and average speed and power output were controlled by modulating coasting duration. This fixed-gear gait may accommodate muscle level constraints on power production. At higher speeds bluegills switched to a mixed power-modulation strategy, increasing speed and power through increased propulsive cycle frequency and reduced coasting time.
“…This stems in part from the scarcity of data for unconstrained, volitional swimming. The combined availability of large-volume calibration techniques recently applied to quantify avian flight performance in the field [11] and low-cost underwater cameras has enabled the collection of field performance data for fish [5,12] with higher temporal and spatial resolution than has previously been possible [1]. This approach has revealed the use of intermittent propulsion during routine, sustained locomotion at aerobically sustained speeds and propulsive cycle frequencies, but with insufficient detail to indicate why this swimming style is used [5].…”
Bluegill sunfish use intermittent propulsion during volitional swimming. The function of this propulsive mode during routine swimming has not been well quantified. At low speeds, propulsive cycle frequencies and amplitudes were constant, and average speed and power output were controlled by modulating coasting duration. This fixed-gear gait may accommodate muscle level constraints on power production. At higher speeds bluegills switched to a mixed power-modulation strategy, increasing speed and power through increased propulsive cycle frequency and reduced coasting time.
“…However, animals rarely travel at these maximal speeds, for example, assuming a slower speed when moving undisturbed through their environment while foraging or during dispersal (Wilson et al, 2015). Locomotion is costly (Di Santo et al, 2017;Han et al, 2017), and the energetic cost (cost of transport, CoT) associated with moving at different speeds may impact the speed adopted by an individual (Claireaux et al, 2006;Halsey, 2016). Limited resources may lead to an allocation trade-off so that allocation of energy to locomotion can constrain energy available for other functions (Lailvaux and Husak, 2014).…”
The energy used to move a given distance (cost of transport; CoT) varies significantly between individuals of the same species. A lower CoT allows animals to allocate more of their energy budget to growth and reproduction. A higher CoT may cause animals to adjust their movement across different environmental gradients to reduce energy allocated to movement. The aim of this project was to determine whether CoT is a repeatable trait within individuals, and to determine its physiological causes and ecological consequences. We found that CoT is a repeatable trait in zebrafish (Danio rerio). We rejected the hypothesis that mitochondrial efficiency (P/O ratios) predicted CoT. We also rejected the hypothesis that CoT is modulated by temperature acclimation, exercise training or their interaction, although CoT increased with increasing acute test temperature. There was a weak but significant negative correlation between CoT and dispersal, measured as the number of exploration decisions made by fish, and the distance travelled against the current in an artificial stream. However, CoT was not correlated with the voluntary speed of fish moving against the current. The implication of these results is that CoT reflects a fixed physiological phenotype of an individual, which is not plastic in response to persistent environmental changes. Consequently, individuals may have fundamentally different energy budgets as they move across environments, and may adjust movement patterns as a result of allocation trade-offs. It was surprising that mitochondrial efficiency did not explain differences in CoT, and our working hypothesis is that the energetics of muscle contraction and relaxation may determine CoT. The increase in CoT with increasing acute environmental temperature means that warming environments will increase the proportion of the energy budget allocated to locomotion unless individuals adjust their movement patterns.
“…For instance, intermittent swimming in fishes is an example of a potentially energy‐saving behaviour at steady, sustainable swimming speeds (Floryan et al ., 2017; Zhao & Dou, 2020). Field and laboratory observations of volitional swimming fish have demonstrated that fish routinely employ intermittent swimming behaviour during aerobically sustainable swimming (Cathcart et al ., 2017; Ellerby et al ., 2018; Gellman et al ., 2019; Han et al ., 2017; Noda et al ., 2016). Modelling suggests that sustained swimming in an intermittent manner ( i.e ., short duration pulpulsive periods of two to three tailbeats interspersed with ~1.0 s glide periods) reduces the energy costs of locomotion (Floryan et al ., 2017; Zhao & Dou, 2020).…”
Group swimming size influences metabolic energy consumption and swimming behaviour in fishes. Hydrodynamic flows and vortices of other fish are thought to be beneficial in terms of the energetic costs of swimming. Similarly, abiotic obstructions have been shown to have similar benefits with respect to metabolic consumption in swimming fish such as rainbow trout Oncorhynchus mykiss. The current study works to examine metabolic rates and swimming behaviours as a function of group swimming with bluegill sunfish Lepomis macrochirus and O. mykiss. Fishes were subjected to individual and group swimming in a respiratory swim tunnel to determine oxygen consumption as a proxy for the metabolic rate of swimming fish. In addition, fish movements within the swim tunnel test chamber were tracked to examine group swimming behaviour. We hypothesized that fish would benefit metabolically from group swimming. In the case of O. mykiss, we also hypothesized that groups would benefit from the presence of an abiotic structure, as has been previously observed in fish swimming individually. Our results suggest that the influence of group size on swimming metabolism is species specific. While L. macrochirus show decreased metabolic rate when swimming in a group compared to individually, O. mykiss did not show such a metabolic benefit from group swimming.
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