Effect of Salinity on the Swimming Velocity of the Water FleaDaphnia magna

1998 ◽  
Vol 71 (6) ◽  
pp. 703-707 ◽  
Author(s):  
Marc Baillieul ◽  
Bart De Wachter ◽  
Ronny Blust
Keyword(s):  
Swimming Velocity

Effects of Moderate Dietary Manipulations on Swim Performance and on Blood Lactate-Swimming Velocity Curves

1999 ◽  
Vol 20 (02) ◽  
pp. 93-97 ◽  
Author(s):  
T. Reilly ◽  
V. Woodbridge
Keyword(s):  
Blood Lactate ◽  
Swimming Velocity ◽  
Swim Performance

scholarly journals Pacing Strategies of 1500 m Freestyle Swimmers in the World Championships According to Their Final Position

2021 ◽  
Vol 18 (14) ◽  
pp. 7559
Author(s):  
Beatriz Lara ◽  
Juan Del Coso
Keyword(s):  
Swimming Velocity ◽  
Final Position ◽  
Men And Women ◽  
Elite Swimmers ◽  
Pacing Strategies ◽  
The World ◽  
Total Data ◽  
Fast Start ◽  
Long Course ◽  
Competitive Swimmers

In 1500 m freestyle swimming races, pacing is generally represented by a parabolic or U-shaped curve indicating that swimming velocity is greatest at the start and the last laps of the race while swimmers maintain an even pace through the middle section of the race. However, there is no information to determine if 1500 m race winners select pacing different to other, less successful swimmers within the same competition. Therefore, this investigation aimed to describe the pacing strategies adopted by 1500 m freestyle competitive swimmers in World Championships (long course), from 2003 to 2019 to determine the most effective pacing to obtain victory or a medal. The official overall and split times for 1500 m freestyle races of the Fédération Internationale de Natation (FINA) were obtained from the website of this organization. In total, data of 143 swimming performances (71 male and 72 female) were extracted. With the split times, lap times, and position were calculated across the race. To determine differences in the pacing between best- and worst-ranked finalist, swimmers in each race were divided into four groups based on the final position (1st vs. 2nd vs. 3rd vs. 4–8th). All the lap times of the winners of the race were faster than those of participants classified as 4–8th position for men and women races (p < 0.05). However, there were no differences in lap velocity among the different positions achieved at the end of the race when it was normalized by average race velocity. Additionally, there were no differences in the lap-to-lap variability among swimmers with different positions at the end of the race. In summary, both men and women elite swimmers selected parabolic pacing consisting of a fast start in the first lap, an even pace close to their average race velocity in the mid-section of the race (from 50 to 1400 m), followed by an end spurt in the final lap(s). This pattern was very similar in all finalists irrespective of the final position in the race. Hence, the obtaining of a medal in the World Championships was associated to possessing a faster average race velocity rather than a specific pacing profile through the race.

Effect of the Pacing Strategies on the Open-Water 10-km World Swimming Championships Performances

2018 ◽  
Vol 13 (6) ◽  
pp. 694-700 ◽  
Author(s):  
Luis Rodriguez ◽  
Santiago Veiga
Keyword(s):  
Open Water ◽  
Public Domain ◽  
Swimming Velocity ◽  
The Public ◽  
Pacing Strategies ◽  
Race Performance

Purpose: To (1) compare the pacing strategies of different-level open-water swimmers during the 10-km race of the FINA 2015 Swimming World Championships and (2) relate these pacing strategies to the race performance. Methods: Final and intermediate split times, as well as intermediate race positions, from the 10-km race participants (69 men and 51 women) were collected from the public domain and were divided into 5 groups (G1–G5) depending on their finishing positions. Results: Medalists and finalists (G1 and G2, respectively) presented an even pacing profile with swimming velocities similar to those of the less successful swimmers (G3–G5) on the initial and middle stages of the race but a 1.5–3% increase in swimming velocity in the last quarter of the race. This acceleration toward the end of the race, or “end spurt,” was largely related to the race performance and was not observed in the G3 and G4 (even-paced profile) or G5 (positive pacing profile) groups. Intermediate race positions and lap rankings were negatively related to finishing position, indicating a delayed positioning of the most successful swimmers at 25%, 50%, and 75% of race distance. Conclusions: The adoption of a conservative starting strategy by open-water swimmers with a negative pacing profile and delayed partial positioning seems to increase the chances of overall race success, as it allows a fast end spurt that is closely related to successful finishing race positions.

Relationships Between Propulsion and Anthropometry in Paralympic Swimmers

2015 ◽  
Vol 10 (8) ◽  
pp. 978-985 ◽  
Author(s):  
Andrew A. Dingley ◽  
David B. Pyne ◽  
Brendan Burkett
Keyword(s):  
Surface Area ◽  
Muscle Mass ◽  
Physical Disability ◽  
Swimming Performance ◽  
Upper Body ◽  
Swimming Velocity ◽  
Frontal Surface ◽  
Anthropometric Measures ◽  
Arm Span ◽  
Upper Body Power

Purpose:To characterize relationships between propulsion, anthropometry, and performance in Paralympic swimming.Methods:A cross-sectional study of swimmers (13 male, 15 female) age 20.5 ± 4.4 y was conducted. Subject locomotor categorizations were no physical disability (n = 8, classes S13–S14) and low-severity (n = 11, classes S9–S10) or midseverity disability (n = 9, classes S6–S8). Full anthropometric profiles estimated muscle mass and body fat, a bilateral swim-bench ergometer quantified upper-body power production, and 100-m time trials quantified swimming performance.Results:Correlations between ergometer mean power and swimming performance increased with degree of physical disability (low-severity male r = .65, ±0.56, and female r = .68, ±0.64; midseverity, r = .87, ±0.41, and r = .79, ±0.75). The female midseverity group showed nearperfect (positive) relationships for taller swimmers’ (with a greater muscle mass and longer arm span) swimming faster, while for female no- and low-severity-disability groups, greater muscle mass was associated with slower velocity (r = .78, ±0.43, and r = .65, ±0.66). This was supported with lighter females (with less frontal surface area) in the low-severity group being faster (r = .94, ±0.24). In a gender contrast, low-severity males with less muscle mass (r = -.64, ±0.56), high skinfolds (r = .78, ±0.43), a longer arm span (r = .58, ±0.60) or smaller frontal surface area (r = -.93, ±0.19) were detrimental to swimming-velocity production.Conclusion:Low-severity male and midseverity female Paralympic swimmers should be encouraged to develop muscle mass and upper-body power to enhance swimming performance. The generalized anthropometric measures appear to be a secondary consideration for coaches.

Responses to Intermittent Swimming Sets at Velocity Associated With max

2005 ◽  
Vol 30 (5) ◽  
pp. 543-553 ◽  
Author(s):  
Sebastien Libicz ◽  
Belle Roels ◽  
Gregoire P. Millet
Keyword(s):  
Oxygen Consumption ◽  
Maximal Oxygen Consumption ◽  
Interval Training ◽  
Swimming Velocity ◽  
Time Duration ◽  
Incremental Test ◽  
Large Variability ◽  
Equal Time ◽  
Physiological Adaptations ◽  
The Times

While the physiological adaptations following endurance training are relatively well understood, in swimming there is a dearth of knowledge regarding the metabolic responses to interval training (IT). The hypothesis tested predicted that two different endurance swimming IT sets would induce differences in the total time the subjects swam at a high percentage of maximal oxygen consumption [Formula: see text]. Ten trained triathletes underwent an incremental test to exhaustion in swimming so that the swimming velocity associated with [Formula: see text][Formula: see text] could be determined. This was followed by a maximal 400-m test and two intermittent sets at [Formula: see text] (a) 16 × 50 m with 15-s rest (IT50); (b) 8 × 100 m with 30-s rest (IT100). The times sustained above 95% [Formula: see text] (68.50 ± 62.69 vs. 145.01 ± 165.91 sec) and 95% HRmax (146.67 ± 131.99 vs. 169.78 ± 203.45 sec, p = 0.54) did not differ between IT50 and IT100 (values are mean ± SD). In conclusion, swimming IT sets of equal time duration at [Formula: see text] but of differing work-interval durations led to slightly different [Formula: see text] and HR responses. The time spent above 95% of [Formula: see text]max was twice as long in IT100 as in IT50, and a large variability between mean [Formula: see text] and HR values was also observed. Key words: interval training, maximal oxygen consumption, triathletes

Interactive effects of salinity on metabolic rate, activity, growth and osmoregulation in the euryhaline milkfish (Chanos chanos)

1998 ◽  
Vol 201 (24) ◽  
pp. 3355-3366
Author(s):  
C Swanson
Keyword(s):  
Metabolic Rate ◽  
High Salinity ◽  
Swimming Performance ◽  
Interactive Effects ◽  
Routine Activity ◽  
Swimming Velocity ◽  
Activity Levels ◽  
Salinity Adaptation ◽  
Chanos Chanos ◽  
Wide Range

The euryhaline milkfish (Chanos chanos) is an excellent subject for studies of the physiological and behavioral processes involved in salinity adaptation. In this study, energy partitioning for metabolism, activity and growth, maximal activity performance and blood osmotic concentrations were assessed at two activity levels in juvenile milkfish fed equal rations and maintained at a relatively constant temperature (262 C) and at salinities(15, 35 and 55 ?) that represented a wide range of osmoregulatory challenges. Changes in the measured parameters were not consistently related to the magnitude of the trans-integumentary osmotic gradients. Routine oxygen consumption rates were high in 35 ? salinity (mean 1 s.e.m. 1678 mg O2 kg-1 h-1) and comparably low in 15 and 55 ? salinity (1336 and 1273 mg O2 kg-1 h-1, respectively). Routine activity levels (relative swimming velocity) were highest in 35 ? salinity (0. 960.04 L s-1), where L is standard length, intermediate in 15 ? salinity (0.770.03 L s-1) and lowest in 55 ? salinity (0.670.03 L s-1). Growth was significantly higher in 55 ? salinity (3.40.2 % increase in wet body mass per day) than in 35 ?salinity (2.40.2 % increase per day) and intermediate in 15 ? salinity(2.90.5 % increase per day). Maximum swimming velocities decreased with increases in salinity, from 9.90.7 L s-1 in 15 ? salinity to 6.60. 5 L s-1 in 55 ? salinity. Sustained swimming activity above routine levels for 2 h resulted in an increase in blood osmotic concentrations in milkfish in 55 ?salinity, but osmoregulation was re-established during the second 2 h of activity. Thus, patterns of variation in metabolic rate and growth were largely parallel to variations in routine activity although, comparing 15 and 55 ? salinity, elevated maintenance costs for osmoregulation at the high salinity were detectable. Reduced osmoregulatory abilities and reductions in maximal swimming performance suggest that high salinity may constrain activity. The results demonstrate that investigations of salinity adaptation in euryhaline fishes should take into account the interactive effects of salinity on physiology and behavior.

The functional allometry of semicircular canals, fins, and body dimensions in the juvenile centrarchid fish, Lepomis gibbosus (L.)

Development ◽  
1973 ◽  
Vol 29 (3) ◽  
pp. 721-743
Author(s):  
Howard C. Howland ◽  
Joseph Masci
Keyword(s):  
Body Mass ◽  
Semicircular Canal ◽  
Semicircular Canals ◽  
Lepomis Gibbosus ◽  
Swimming Velocity ◽  
Body Dimensions ◽  
Moments Of Inertia ◽  
Significant Difference ◽  
Vertical Semicircular Canal ◽  
Vertical Semicircular Canals

1. The ontogenetic allometry of radii of curvature and the tube radii of the semicircular canals of approximately 85 juvenile (2–20 g) centrarchids of the species Lepomis gibbosus (L.) was investigated. The radii of curvature of the semicircular canals have different allometries; these arefor the anterior vertical, posterior vertical and horizontal canals respectively. The differences in growth exponents between the anterior and posterior vertical semicircular canals and between the anterior vertical and horizontal semicircular canals were statistically significant (P &lt; 0·02 and P &lt; 0·05 respectively). 2. Body mass and standard length were almost equally good predictors of the radii of curvature of the anterior vertical semicircular canals, but body mass was the better predictor of the radii of curvature of the posterior vertical and horizontal semicircular canals, as judged by the magnitude of the mean squares about the logarithmic regressions of radii on length and mass. 3. By measuring and estimating the area moments of the fins of the fish, the moments of inertia about various axes and the allometry of the characteristic swimming velocity of the fish, we attempted to account for the magnitude and direction of the differences in allometric growth exponents of the radii of curvature of the semicircular canals. Unexplained by our best estimate of growth exponents was the very high value observed for the posterior vertical semicircular canals. 4. No significant correlation could be found between the residuals of the major dimensions of the posterior vertical semicircular canals and those of body width or depth once the influence of body mass was removed. This finding suggests the rejection of the hypothesis that the allometry of this semicircular canal is simply correlated with overall body expansion in its plane. 5. The discrepancies between our predictions and observations of growth exponents could be explained by a gradual increase of the spring constant of the semicircular canals on the order ofthough they may also be due to other factors neglected in our model, e.g. the allometry of the added mass of the fish. 6. No evidence suggested that the shape of the semicircular canals was altered over the size range of the fish we studied. However, among the fins of the fish and the major body dimensions, only the width and the depth of the fish exhibited growth constants that did not differ significantly from each other. 7. We computed the effective toroidal radii of the non-toroidal-shaped vertical semicircular canals and found that the equivalent toroidal radius of the anterior vertical semicircular canal was consistently greater than that of the posterior vertical semicircular canal. This difference is explicable on the basis of the different moments of inertia of the animal about axes through the center of gravity and parallel to the axes of the semicircular canals. 8. We computed the allometry of the ratios R̄/r2 for all three semicircular canals and found in accordance with the prediction of Jones & Spells that they did not differ significantly from zero. 9. The allometry of the outer tube radii of the several semicircular canals was determined, and, while there was no significant difference in the growth exponents of the tube radii, it was noted that the tube radius of the horizontal semicircular canal was consistently and significantly smaller than that of the vertical semicircular canal. We suggested that this difference might be due to the broader range of frequencies that the fish experienced about its yaw axis. 10. Taken as a whole the data and calculations of this paper generally support the theory that the dimensions of the semicircular canals and the ontogenetic changes in them attune the semicircular canals to the angular frequency spectra that the fish experience about their axes.

BLIND MEXICAN CAVE FISH (ASTYANAX HUBBSI) RESPOND TO MOVING VISUAL STIMULI

1994 ◽  
Vol 188 (1) ◽  
pp. 89-101 ◽  
Author(s):  
T Teyke ◽  
S Schaerer
Keyword(s):  
Visual Stimulus ◽  
Swimming Velocity ◽  
Environmental Cues ◽  
Cave Fish ◽  
Optomotor Response ◽  
Aquarium Fish ◽  
Modified Theory ◽  
Test Aquarium ◽  
Optomotor Behaviour

In apparatus for measuring optomotor behaviour, blind Mexican cave fish, Astyanax hubbsi, increase their swimming velocity upon rotation of a striped cylinder, i.e. in response to a solely visual stimulus. The fish follow the movements of the stripes at (i) rotation velocities between 60 degrees s-1 and 80 degrees s-1, (ii) light intensities of less than 20 lx and, (iii) stimulus widths subtending an angle of less than 1 &deg;. Extirpation of the vestigial eye structures does not affect the response to the moving visual stimulus, which indicates that the response is mediated by extra-ocular photoreceptors. An optomotor response can be reliably evoked in a round test aquarium. Fish do not respond when the test aquarium contains environmental cues, such as bars on the wall or when a section of the round aquarium is divided off. This indicates that the fish obtain information about their environment from different sensory sources and that the visual stimulus is effective only when no other means of orientation are available. We suggest a modified theory of the optomotor response, which emphasizes the crucial role of the environment in eliciting the response and which permits behaviours more complex than just following the stimulus.

Swimming of the Trophont Zooid of Vorticella Convallaria

2021 ◽  
Author(s):  
Dilziba Kizghin ◽  
Sangjin Ryu ◽  
Younggil Park ◽  
Sunghwan Jung
Keyword(s):  
Mean Square Displacement ◽  
Swimming Velocity ◽  
Mean Square ◽  
Ciliated Protozoan ◽  
Swimming Motility ◽  
Swimming Motion ◽  
Swimming Pattern ◽  
Freshwater Habitats ◽  
Gap Height ◽  
Swimming Trajectories

Abstract Vorticella convallaria is a ciliated protozoan found in freshwater habitats. In the sessile or stalked trophont form, V. convallaria is shaped somewhat like a balloon as it has a body or zooid (the head of the balloon) that is about 40 μm large with cilia around its oral part, and a stalk (the string of a balloon) anchoring the zooid to a solid surface. When a trophont zooid of V. convallaria detached from the stalk, the zooid swims around in water by creating water flow using its oral cilia. In contrast to the stalk contraction of V. convallaria that has been well studied, the swimming motility of V. convallaria is little known. In this study, we measured the swimming trajectories of the stalkless trophont zooid of V. convallaria using video microscopy and Hele-Shaw cells with a gap height of 25 μm, traced the swimming zooid using image processing, and analyzed the swimming motion in terms of swimming velocity and mean square displacement. The stalkless trophont zooid of V . convallaria was found to swim in circular patterns with intermittent ballistic motions in the confinement, and the average swimming speed ranged from 20 μm/s to 110 μm/s. Since the swimming pattern of V. convallaria appeared to be affected by the level of confinement, we will continue characterizing the ciliate’s swimming in the Hele-Shaw cell with different gap heights. Our study is expected to reveal the swimming motility of V. convallaria and to advance general understanding of swimming of microorganisms.

Metabolic and energy correlates of intracellular pH in progressive fatigue of squid (L. brevis) mantle muscle

1996 ◽  
Vol 271 (5) ◽  
pp. R1403-R1414 ◽  
Author(s):  
H. O. Portner ◽  
E. Finke ◽  
P. G. Lee
Keyword(s):  
Free Energy ◽  
Critical Velocity ◽  
Energy Levels ◽  
High Energy ◽  
Swimming Velocity ◽  
High Energy Phosphates ◽  
Energy Status ◽  
Intracellular Acidosis ◽  
Model Calculations

Squid (Lolliguncula brevis) were exercised at increasing swimming speeds to allow us to analyze the correlated changes in intracellular metabolic, acid-base, and energy status of the mantle musculature. Beyond a critical swimming velocity of 1.5 mantle lengths/s, an intracellular acidosis developed that was caused by an initial base loss from the cells, the onset of respiratory acidification, and, predominantly, octopine formation. The acidosis was correlated with decreasing levels of phospho-L-arginine and, thus, supported ATP buffering at the expense of the phosphagen. Monohydrogenphosphate, the actual substrate of glycogen phosphorylase accumulated, enabling glycogen degradation, despite progressive acidosis. In addition to octopine, succinate, and glycerophosphate accumulation, the onset of acidosis characterizes the critical velocity and indicates the transition to a non-steady-state time-limited situation. Accordingly, swimming above the critical velocity caused cellular energy levels (in vivo Gibbs free energy change of ATP hydrolysis) to fall. A minimal value was reached at about -45 kJ/mol. Model calculations demonstrate that changes in free Mg2+ levels only minimally affect ATP free energy, but minimum levels are relevant in maintaining functional concentrations of Mg(2+)-complexed adenylates. Model calculations also reveal that phosphagen breakdown enabled L. brevis to reach swimming speeds about three times higher than the critical velocity. Comparison of two offshore squid species (Loligo pealei and Illex illecebrosus) with the estuarine squid L.brevis indicates that the latter uses a strategy to delay the exploitation of high-energy phosphates and protect energy levels at higher than the minimum levels (-42 kJ/mol) characterizing fatigue in the other species. A more economical use of anaerobic resources and an early reduction in performance may enable L. brevis to tolerate more extreme environmental conditions in shallow estuarine waters and even hypoxic environments and to prevent a fatal depletion of energy stores.

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