Stenotherms at sub-zero temperatures: thermal dependence of swimming performance in Antarctic fish

We examined the burst swimming performance of two Antarctic fishes, Trematomus bernacchii and T. centronotus, at five temperatures between -1 degrees C and 10 degrees C. As Antarctic fishes are considered one of the most cold specialised and stenothermal of all ectotherms, we predicted they would possess a narrow thermal performance breadth for burst swimming and a correlative decrease in performance at high temperatures. Burst swimming was assessed by videotaping swimming sequences with a 50-Hz video camera and analysing the sequences frame-by-frame to determine maximum velocity, the distance moved throughout the initial 200 ms, and the time taken to reach maximum velocity. In contrast to our prediction, we found both species possessed a wide thermal performance breadth for burst swimming. Although maximum swimming velocity for both T. bernacchii and T. centronotus was significantly highest at 6 degrees C, maximum velocity at all other test temperatures was less than 20% lower. Thus, it appears that specialisation to a highly stable and cold environment is not necessarily associated with a narrow thermal performance breadth for burst swimming in Antarctic fish. We also examined the ability of the Antarctic fish Pagothenia borchgrevinki to acclimate their burst-swimming performance to different temperatures. We exposed P. borchgrevinki to either -1 degrees C or 4 degrees C for 4 weeks and tested their burst-swimming performance at four temperatures between -1 degrees C and 10 degrees C. Burst-swimming performance of Pagothenia borchgrevinki was unaffected by exposure to either -1 degrees C or 4 degrees C for 4 weeks. Maximum swimming velocity of both acclimation groups was thermally independent over the total temperature range of 1 degrees C to 10 degrees C. Therefore, the loss of any capacity to restructure the phenotype and an inability to thermally acclimate swimming performance appears to be associated with inhabiting a highly stable thermal environment.     

The swimming abilities of recently settled post-larvae of Sillaginodes punctata

Sixty-four post-larvae of the King George whiting Sillaginodes punctata were tested in swimming chambers, against one of five flow-through velocities (2, 4, 6, 8 or 10 cm s ⁻¹) for up to a maximum of 120 min. Fish were determined by regression to have an FV₅₀ (50% fatigue velocity) of 6.0 cm s⁻¹. No fish survived the full 120 min at 10 cm s⁻¹. Sixteen individuals were tested in a swimming chamber against a flow-through velocity of 6 cm s ⁻¹ and allowed to swim to exhaustion. Fish swam between 25 and 538 min with a peak at c . 6–8 h. Total swimming time was not correlated with standard length of fish although the size range examined was narrow. Relative to recent studies on the swimming abilities of late-stage larvae of reef fishes, this study indicates that post-larval King George whiting are weak swimmers. The weak swimming ability of post-larval King George whiting is consistent with studies showing passive dispersal and recruitment of this species.     

Numerical model for the locomotion of spirilla

The swimming of trailing, leading, and bipolar spirilla (with realistic flagellar centerline geometries) is considered. A boundary element method is used to predict the instantaneous swimming velocity, counter-rotation angular velocity, and power dissipation of a given organism as functions of time and the geometry of the organism. Based on such velocities, swimming trajectories have been deduced enabling a realistic definition of mean swimming speeds. The power dissipation normalized in terms of the square of the mean swimming speed is considered to be a measure of hydrodynamic efficiency. In addition, kinematic efficiency is defined as the extent of deviation of the swimming motion from that of a previously proposed ideal corkscrew mechanism. The dependence of these efficiencies on the organism's geometry is examined giving estimates of its optimum dimensions. It is concluded that appreciable correlation exists between the two alternative definitions for many of the geometrical parameters considered. Furthermore, the organism having the deduced optimum dimensions closely resembles the real organism as experimentally observed.     

Spawning behaviour and diel periodicity of egg production in captive Atlantic mackerel,Scomber scombrus L.*

Spawning was observed in groups of captive Atlantic mackerel and occurred when a few fish swam away from the main school during a brief burst of high speed swimming. Counts of eggs from aquarium and field studies show that, in contrast to most pelagic fish species, spawning by Atlantic mackerel can occur at any time ofday or night and is not group-synchronized. Implications of the observed die1 periodicity of egg production to stock size estimation by the Daily Egg Production Method are discussed.     

Intra-school positional preference and reduced tail beat frequency in trailing positions in schooling roach under experimental conditions

Using three different swimming velocities and a school size of eight roach Rutilus rutilus , individual intra-school position and tail beat frequency were examined in a flume tank. Tail beat frequency was determined in defined leading and trailing positions. Individual roach showed consistent intra-school positional preferences which implied a sustained positional pattern where certain individuals took up front positions whereas other individuals swam in the rear part of the school. The positional preferences could not be attributed to inter-individual differences of the eight roach in terms of total length, mass or condition factor. At the tested swimming velocities of 2, 3 and 4  L _T s⁻¹, roach in trailing positions swam with tail beat frequencies reduced by 7·3, 11·9 and 11·6%, respectively, compared to roach in leading positions. These results suggested that roach situated in trailing positions experienced energetic savings due to hydrodynamic interactions at a wide range of swimming velocities. This may be important during migrations or when a school of roach is holding its position against the current in a lotic habitat. The observed sustained positional pattern combined with a hydrodynamic advantage in trailing positions would indicate that these energetic savings might not be evenly shared among schoolmates of roach. A positive correlation between swimming velocity and stride length was found. The present study, however, does not support any conclusions concerning these findings.     

Influence of the concentration of oxygen on the swimming path of Brachionus plicatilis (Rotifera)

Brachionus plicatilis females were maintained for > 24 hours in water where the concentration of oxygen was precisely controlled (spherical flasks with 6 mg l^–1 or < 0.5 mg l^–1; food = dead Tetraselmis sp.). Each female was randomly taken from one flask and quickly placed in an observation chamber containing the same experimental conditions. The swimming path was videotaped (5 minutes); then the size of the female was measured. The tape was analyzed by automatic tracking (25 x,y coordinates of the center of the animal, in a 512 × 512 pixels space). The swimming path was analyzed for 45 females in both treatments. The speed (mm s^–1 body length^–1) was calculated for all trajectories, or only for those segments where females swam in a horizontal plane. This relative speed significantly decreased when the concentration of oxygen was very low. There was a negative correlation between the linear speed and the angular speed. The spatial sinuosity (S of Bovet & Benhamou, 1988) was calculated. The trajectories were significantly more sinuous when the concentration of oxygen was very low. These results could explain the accumulation of some rotifers in the oxycline; rotifers may spend more time in very low concentrations of oxygen by slowing and by turning more.     

Two-phase exploration of a novel environment in the guppy, Poecilia reticulata

Swimming speed and percentage of time fish swam along the boundary of an aquarium gradually decreased with the time following release of juvenile guppies into unfamiliar surroundings. When swimming speed was plotted against time on a log scale, two distinct phases were identified. The high activity phase lasted c, 3 h in 30-day-old guppies, 6 h in 10-day-olds and not less than S h in 3-day-olds. Observed trends in swimming in guppies are interpreted as a component of exploratory behaviour. Alternating the surroundings confirmed the exploratory role of such swimming and suggested that a period of general exploration was followed by a period of more detailed investigation of habitat. An interaction between exploratory and avoidance (fear) responses is discussed.     

Power isn't everything: muscle function and energetic costs during steady swimming in Atlantic cod (Gadus morhua)

Power produced by red myotomal muscles of fish during cruise swimming appears seldom maximized, so we sought to investigate whether economy may impact or dominate muscle function. We measured cost of transport (COT) using oxygen consumption and the strain trajectories and electromyographic activity of red muscle measured at anterior (ANT) and posterior (POST) locations while Atlantic cod (Gadus morhua) swam steadily at speeds between 0.3 and 1.0 body lengths (BL) s(-1). We then measured the power produced by isolated segments of red muscle when activated either as in the swimming cod or such that maximal net power was produced. Patterns of activation during swimming were not optimal for power output and were highly variable between tail beats, particularly at the ANT location and at slow swim speeds. Muscle strain amplitude did not increase until swimming speed reached 0.9 (ANT) versus 0.5 (POST) BL s(-1). These limited power to only 53% (ANT) and 71% (POST) of maximum at slower swim speeds and to 70%-80% of maximum at high swim speeds. COT (resting metabolism subtracted) was minimal at the slowest swim speed, surprisingly, where power was most impaired by activation and strain. Thus, production of powered forces for maneuverability/stability appeared to greatly impact red muscle function during cruise swimming in cod, particularly at slow speeds and in ANT muscle.     

Evidence for a correlation between swimming velocity and membrane fluidity of Tetrahymena cells

The influence of the physical state of the membrane on the swimming behaviour of Tetrahymena pyriformis was studied in cells with lipid-modified membranes. When the growth temperature of Tetrahymena cells was increased from 15 degrees C to 34 degrees C or decreased from 39 degrees C to 15 degrees C, their swimming velocity changed gradually in a similar to the adaptive change in membrane lipid composition. Therefore, such adaptive changes in swimming velocity were not observed during short exposures to a different environment. Tetrahymena cells adapted to 34 degrees C swam at 570 microns/s. On incubation at 15 degrees C these cells swam at 100 microns/s. When the temperature was increased to 34 degrees C after a 90-min incubation at 15 degrees C, the initial velocity was immediately recovered. On replacement of tetrahymanol with ergosterol, the swimming velocity of 34 degrees C-grown cells decreased to 210 microns/s, and the cells ceased to move when the temperature was decreased to 15 degrees C. To investigate the influence of the physical state of the membrane on the swimming velocity, total phospholipids were prepared from Tetrahymena cells grown under these different conditions. The fluidities of liposomes of these phospholipid were measured using stearate spin probe. The membrane fluidity of the cells cooled to 15 degrees C increased gradually during incubation at 15 degrees C. On the other hand, the fluidity of the heated cell decreased during incubation at 34 degrees C. Replacement of tetrahymanol with ergosterol decreased the membrane fluidity markedly. Consequently, a good correlation was observed between swimming velocity and membrane fluidity; as the membrane fluidity increased, the swimming velocity increased linearly up to 600 microns/s. These results provide evidence for the regulation of the swimming behaviour by physical properties of the membrane.     

Dynamic Resistance Parameters of Arm Stroke during Swimming

Swimming, as a sport beneficial to body and mind, also has a place in international sports. For swimmers and coaches, it is always the most important to improve the propulsion and reduce the resistance during swimming. This paper briefly introduced the resistance of human body in swimming, described the dynamic resistance of human body in arm stroke, and then introduced the principle of micro disturbance method which was used for measuring the dynamic resistance in swimming. Finally, ten swimmers from school team and ten beginners were tested for the dynamic resistance in freestyle, backstroke and breaststroke when they swam with arm stroke only. After adding micro resistance, the swimming speed of the subjects decreased when they swam with all their strength; the speed of freestyle swimming was the largest, followed by backstroke and breaststroke before and after loading, and the swimming speed of school team members was larger than that of beginners; the dynamic resistance and dynamic resistance coefficient of breaststroke were the largest, backstroke was the second, freestyle was the smallest, and the dynamic resistance and dynamic resistance coefficient of school team members were always smaller than those of beginners no matter the swimmer took which swimming style.     

Swimming performance is reduced by reflective markers intended for the analysis of swimming kinematics

The present study aimed to clarify whether swimming performance is affected by reflective markers being attached to the swimmer’s body, as is required for a kinematic analysis of swimming. Fourteen well-trained male swimmers (21.1 ± 1.7 yrs) performed maximal 50 m front crawl swimming with (W) and without (WO) 25 reflective markers attached to their skin and swimwear. This number represents the minimum required to estimate the body’s center of mass. Fifty meter swimming time, mid-pool swimming velocity, stroke rate, and stroke length were determined using video analysis. We found swimming time to be 3.9 ± 1.6% longer for W condition. Swimming velocity (3.3 ± 1.8%), stroke rate (1.2 ± 2.0%), and stroke length (2.1 ± 2.7%) were also significantly lower for W condition. To elucidate whether the observed reduction in performance was potentially owing to an additional drag force induced by the reflective markers, measured swimming velocity under W condition was compared to a predicted velocity that was calculated based on swimming velocity obtained under WO condition and an estimate of the additional drag force induced by the reflective markers. The mean prediction error and ICC (2,1) for this analysis of measured and predicted velocities was 0.014 m s⁻¹ and 0.894, respectively. Reducing the drag force term led to a decrease in the degree of agreement between the velocities. Together, these results suggest that the reduction in swimming performance resulted, at least in part, from an additional drag force produced by the reflective markers.     

Movement characteristics and acrosomal status of rabbit spermatozoa recovered at the site and time of fertilization

Rabbit spermatozoa were recovered from the oviductal ampullae 11 h postcoitus by an oil microflush technique. Their movement was evaluated in the ampullar fluid, or in ampullar fluid diluted with in vitro fertilization medium, in slide preparations which were approximately 25 micron or 100 micron deep. The movement of these sperm was compared with the movement of ejaculated sperm in diluted semen. Movement parameters measured from videotapes recorded by a high-speed camera were coded according to treatment and entered into a microcomputer for statistical analysis. A total of 157 spermatozoa were recovered from the oviducts of 16 does: 152 were motile and 126 were free-swimming. Nearly all of the free-swimming sperm swam in trajectories whose average paths were circular. The flagellar beat pattern of the circular swimmers was asymmetric and nearly planar, and the sperm did not roll. Spermatozoa observed in 25-micron slide preparations produced smaller flagellar bends than sperm swimming in 100-micron preparations and tended to swim in larger circles which were oriented in the plane of the slide. Spermatozoa observed within the cumulus matrix moved in a slow, erratic, sinuous manner, but resumed rapid circling upon leaving the matrix. It was concluded that the ampullar sperm were hyperactivated, retaining this physiological condition as they entered the cumulus. The movement qualitatively resembled that of hyperactivated guinea pig and hamster spermatozoa because these species effectively swim in circles. In contrast, 80% of the ejaculated spermatozoa swam in linear trajectories, resulting from relatively symmetrical, flagellar beat patterns. The percentage of rolling spermatozoa and the rolling frequencies were less in the 25-micron than the 100-micron slide preparations. Thus, the movement parameters of both ampullar and ejaculated spermatozoa were affected by the geometry of their observation chambers. This influence should be taken into account when observing sperm motility in vitro. It could also be important in vivo, where changes in sperm movement in response to epithelial surfaces might provide an advantage for reaching the cumulus mass. Ninety-eight percent of the motile ampullar sperm were observed to have acrosomes, including all spermatozoa found within the cumulus matrix.     

Role partitioning of swimming musculature of striped Bass Morone saxatilis Walbaum and Bluefish, Pomatomus saltatrix L.

Electromyography was used to determine the functional roles of the axial musculature in striped bass and bluefish at imposed swimming velocities. The lateral red muscle powers propulsive movements at all sustainable swimming speeds in both species. The amplitude and frequency of EMG's from the red muscle grade with increasing swimming velocity. The white muscle, forming the main mass of the myotome, is reserved for high-speed burst swimming above maximum sustainable speeds. The proportion of the myotome occupied by the red muscle at the level of the caudal peduncle is 10.9% and 18.6% for the striped bass and the bluefish respectively.     

Relationship between tethered forces and the four swimming techniques performance

The purpose of the current study was to identify the relationships between competitive performance and tether forces according to distance swam, in the four strokes, and to analyze if relative values of force production are better determinants of swimming performance than absolute values. The subjects (n = 32) performed a 30 s tethered swimming all-out effort. The competitive swimming velocities were obtained in the distances 50, 100 and 200 m using official chronometric values of competitions within 25 days after testing protocol. Mean force and velocity (50 m event) show significant correlations for front crawl (r = .92, p < .01), backstroke (r = .81, p < .05), breaststroke (r = .94, p < .01) and butterfly (r = .92, p < .01). The data suggests that absolute values of force production are more associated to competitive performance than relative values (normalized to body mass). Tethered swimming test seems to be a reliable protocol to evaluate the swimmer stroking force production and a helpful estimator of competitive performance in short distance competitive events.     

Development of net energy intake models for drift-feeding juvenile coho salmon and steelhead

We developed models to predict the effect of water velocity on prey capture rates and on optimal foraging velocities of two sympatric juvenile salmonids, coho salmon and steelhead. Mean fish size was ~80 mm, the size of age I+ coho and steelhead during their second summer in Southeast Alaska streams, when size overlap suggests that competition might be strongest. We used experimentally determined prey capture probabilities to estimate the effect of water velocity on gross energy intake rates, and we modeled prey capture costs using experimental data for search and handling times and published models of swimming costs. We used the difference between gross energy intake and prey capture costs to predict velocities at which each species maximized net energy intake rate. Predicted prey capture rates for both species declined from ~75 to 30–40 prey/h with a velocity increase from 0.30 to 0.60 m·s⁻¹. We found little difference between coho and steelhead in predicted optimum foraging velocities (0.29 m·s⁻¹ for coho and 0.30 m·s⁻¹ for steelhead). Although prey capture ability appears to be more important than are prey capture costs in determining optimum foraging velocities, capture costs may be important for models that predict fish growth. Because coho are assumed to pay a greater swimming cost due to a less hydrodynamic body form, we also modeled 10 and 25% increases in hydrodynamic drag to assess the effect of increased prey capture costs. This reduced optimum velocity by 0 and 0.01 m∙s⁻¹, respectively. Habitat segregation among equal-sized coho and steelhead does not appear to be related to the effects of water velocity on their respective foraging abilities.     

Rainbow trout display a developmental shift in red muscle kinetics, swimming kinematics and myosin heavy chain isoform

Both activation and relaxation times of rainbow trout Oncorhynchus mykiss red muscle were shorter in parr than in older juveniles. Furthermore, parr red muscle had a faster maximum shortening velocity than that of older fish, as estimated with the force-clamp technique. Parr swam with higher tailbeat frequencies and lower tailbeat amplitude than did older fish across a range of length-specific steady swimming speeds. The developmental shift in contraction kinetics of red muscle and steady swimming kinematics was associated with a reduction from two or three myosin heavy chain isoforms in parr to one in older juveniles. This transition provides a mechanism to explain the variations in muscle contraction kinetics and swimming performance.     

Effects of substrate roughening on the swimming performance of Schizothorax wangchiachii (Fang, 1936) in the Heishui River: Implications for vertical slot fishway design

Re-establishing the natural connectivity of rivers using fishways may mitigate the unfavourable effects of dam construction on riverine biodiversity and freshwater fish populations. Knowledge of the swimming performance of target species in specific regions is critical for designing fishways with a high passage efficiency. Substrate roughening with river stones of fishways is considered to improve fish swimming capacity by benefiting from reduced-velocity zones with lower energetic costs. However, the effectiveness of rough substrates in energy metabolism is rarely tested. We investigated the effect of substrate roughening on the swimming capacity, oxygen consumption and behaviour of Schizothorax wangchiachii from the Heishui River in a flume-type swimming respirometer. The results showed that substrate roughening improved critical and burst swimming speed by ~12.9% and ~15.0%, respectively, compared to the smooth substrate. Our results demonstrate that increased reduced-velocity zones, lowered metabolic rate and tail-beat frequency support our hypothesis that lower energetic costs improve fish swimming performance in rough substrate compared to smooth treatment. The traversable flow velocity model predicted that maximum traversable flow velocity and maximum ascent distance were higher over rough compared to smooth substrate fishways. Fishway substrate roughening may be a practical approach to improve fish swimming upstream for demersal riverine fish.     

Flow Loading Induces Oscillatory Trajectories in a Bloodstream Parasite

The dynamics of isolated microswimmers are studied in bounded flow using the African trypanosome, a unicellular parasite, as the model organism. With the help of a microfluidics platform, cells are subjected to flow and found to follow an oscillatory path that is well fit by a sine wave. The frequency and amplitudes of the oscillatory trajectories are dependent on the flow velocity and cell orientation. When traveling in such a manner, trypanosomes orient upstream while downstream-facing cells tumble within the same streamline. A comparison with immotile trypanosomes demonstrates that self-propulsion is essential to the trajectories of trypanosomes even at flow velocities up to ～40 times higher than their own swimming speed. These studies reveal important swimming dynamics that may be generally pertinent to the transport of microswimmers in flow and may be relevant to microbial pathogenesis.     

Physiological Performance and Stream Microhabitat use by the Centrarchids Lepomis megalotis and Lepomis macrochirus

Two centrarchids, Lepomis megalotis and L. macrochirus, were compared in laboratory studies of prey capture success, swimming endurance, morphology, hydrodynamic drag, and thermal tolerance, as well as field observations of focal point velocity and depth. For both species, capture of planktonic prey declined as current velocity increased, but L. megalotis was more efficient than L. macrochirus at higher current velocities. Capture of floating prey was not influenced by current velocity, but L. megalotis was more efficient overall at all velocities. Of the two species, L. megalotis was significantly more streamlined, had relatively lower hydrodynamic drag, and had higher swimming endurance in current. Both species had significantly higher critical thermal maxima (CTMax) in summer than in winter, but variance in CTMax was greater for L. megalotis than for L. macrochirus in both summer and winter. Differences between L. megalotis and L. macrochirus in performance and morphology may have direct influence on their relative abundances in small streams. Field observations showed L. megalotis was more common than L. macrochirus in faster, shallower microhabitats.     

鲢幼鱼在不同水流速度下的暴发-滑行行为策略

在水温（18±1）℃的条件下,以全长（11.70±0.57）cm的鲢（Hypophthalmichthys molitrix）幼鱼为研究对象,测定其不同流速（16.5、22.0、27.5、33.0、38.5、44.0、49.5和55.0 cm/s）下的持续游泳时间、调头百分比和暴发-滑行运动数据。结果表明,鲢的平均持续游泳时间先随流速的增加而减小,后随流速的增加而增加。当流速33.0 cm/s时,平均持续时间最短为118.6min,其中各组试验鱼的最大可持续游泳时间均可达到200min。调头百分比随流速的增加迅速减小,当流速≥44.0 cm/s时,不再出现调头行为。暴发-滑行游泳的平均暴发时间随流速的增加呈上升趋势（y=0.03x+2.64,R2=0.92,P<0.05）。平均对地暴发距离均在30-45 cm,没有显著性差异（P>0.05）,平均绝对暴发距离存在极显著性差异,且随流速的增加而增加（y=4.98x-5.63,R2=0.98,P<0.001）。平均对地暴发速度没有显著性差异（平均对地平均速度和最大速度分别在9-12 cm/s、12-16 cm/s,P>0.05）。平均绝对暴发速度与水流速度之间存在线性正相关关系（平均绝对平均暴发速度:y=0.98x+10.74,R2=1.00,P<0.001;平均绝对最大暴发速度:y=1.02x+13.75,R2=0.99,P<0.001）。研究表明鲢在不同的流速下采取的暴发-滑行行为策略不同。