Comparison of the swimming performance of farmed and wild gilthead sea bream, Sparus aurata

Farmed gilthead sea bream, Sparus aurata, frequently escape from the sea cages and interact with wild populations. The impact of these interactions on the wild populations will depend, in part, on differences in performance of the bream. This study compared the swimming performance of the wild and farmed fish in a current channel. The absolute critical swimming speed (U_crit) increased with increasing size while the relative U_crit decreased. Even at the same length there were noticeable performance differences between the individuals. The wild sea bream have significantly higher (P<0.05) absolute U_crit performance (0.86±0.01 m s⁻¹) than the farmed fish (0.79±0.01 m s⁻¹) and significantly higher (P<0.05) relative U_crit performance (4.52±0.05 BL s⁻¹) than the farmed fish (4.21±0.05 BL s⁻¹). The present study suggests that cultured sea bream may not have the ability to compete with wild sea bream in native seawaters.     

Metabolic measurements and parameter estimations for bioenergetics modelling of Pacific Chub Mackerel Scomber japonicus

As a crucial step in developing a bioenergetics model for Pacific Chub Mackerel Scomber japonicus (hereafter chub mackerel), parameters related to metabolism, the largest dissipation term in bioenergetics modelling, were estimated. Swimming energetics and metabolic data for nine chub mackerel were collected at 14°C, a low temperature within the typical thermal range of this species, using variable‐speed swim‐tunnel respirometry. These new data were combined with previous speed‐dependent metabolic data at 18 and 24°C and single‐speed (1 fork length per second: FL/s) metabolic data at 15 and 20°C to estimate respiration parameters for model development. Based on the combined data, the optimal swimming speed (the swimming speed with the minimum cost of transport, U_opt) was 42.5 cm/s (1.5–3.0 FL/s or 2.1 ± 0.4 FL/s) and showed no significant dependence on temperature or fish size. The daily mass‐specific oxygen consumption rate (R, g O₂ g fish^?1 day^?1) was expressed as a function of fish mass (W), temperature (T) and swimming speed (U): R = 0.0103W^?0.490 e^(0.0457T) e^(0.0235U). Compared to other small pelagic fishes such as Pacific Herring Clupea harengus pallasii, Pacific Sardine Sardinops sagax and various anchovy species, chub mackerel respiration showed a lower dependence on fish mass, temperature and swimming speed, suggesting a greater swimming ability and lower sensitivity to environmental temperature variation.     

Effects of 2-phenoxyethanol on survival of normal juveniles and malformed juveniles having lordosis or nonfunctional swimbladders of European sea bass (Dicentrarchus labrax L., 1758)

The objectives of this study were to evaluate the effects of 2‐phenoxyethanol (2‐PE), which is an anaesthetic, on survival rates of normal juveniles and malformed juveniles having lordosis or nonfunctional swim bladders of European sea bass (Dicentrarchus labrax L., 1758) and to establish the LC₅₀ (the concentration lethal to 50% of test animals at concentrations of 0.05, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4 and 4.5 mL L⁻¹) and LT₅₀ (the time lethal to 50% of test animals after 10‐, 20‐, 30‐, 40‐, 50‐ and 60‐min time periods) of 2‐PE at 19±0.5°C, salinity 38 g L⁻¹, pH 7.4–7.8 and dissolved oxygen >8 mg L⁻¹. Between concentrations of 0.05 and 0.25 mL L⁻¹, 2‐PE did not cause any mortality or toxicity on normal, lordosis and nonfunctional swimbladder juveniles of sea bass during the 60‐min exposure period. On the other hand, significance in each group fish in their mortality rates between concentrations of 0.30 and 0.45 mL L⁻¹ was observed (P<0.05). The nonfunctional swimbladder juveniles showed lower LC₅₀ than normal and lordosis juveniles respectively. Also, nonfunctional swimbladders juveniles showed lower LT₅₀ than normal and lordosis juveniles respectively. At concentrations of 0.30, 0.35, 0.40 and 0.45 mL L⁻¹, induction times were found to be significantly different among the three groups (P<0.05). Recovery times were not found to be significantly different in two groups at concentrations of 0.30 and 0.40 mL L⁻¹ (P>0.05). The toxic effect of 2‐PE on sea bass juveniles increased depending on the exposure times (P<0.05). The most suitable concentrations of 2‐PE were 0.30–0.35 mL L⁻¹ between minutes 10 and 30, although the normal juveniles can resist to 0.45 mL L⁻¹ of 2‐PE concentration for 20 min. The 2‐PE showed toxicity in relation to the concentrations and exposure time combinations among the three groups in the order; nonfunctional swimbladder fish >lordosis fish >normal fish.     

Effects of soft-water acclimation on the physiology, swimming performance, and cardiac parameters of the rainbow trout, Oncorhynchus mykiss

Rainbow trout acclimated to soft water were submitted to an incremental velocity trial, and exhibited a 14% decrease in critical swimming speed (U _crit ∼ 1.37 ± 0.055 vs. 1.54 ± 0.044 m s⁻¹) compared to fish kept in hard water. After a standardized swimming protocol, soft-water-acclimated fish had higher blood lactate concentrations (6.5 ± 0.66 and 6.0 ± 0.64 mmol L⁻¹ (soft water) vs. 5.0 ± 0.46 and 3.9 ± 0.32 mmol L⁻¹ (hard water)), revealing a greater use of anaerobic metabolism for the same exercise. Cardiovascular parameters were investigated while fish were swimming at increasing water velocities, revealing that soft-water-acclimated fish had lower increases in heart rate (105% vs. 118% of pre-exercise values), due to higher heart rates observed during acclimation and during the first 10 min of the swimming trial. This was also reflected by the plateau in heart rate and stroke volume observed during the swimming protocol, which can be attributed to increased cardiovascular function in response to soft-water acclimation. These results are in accord with previously reported increases in blood-to-water diffusion distance, due to proliferation of chloride cells at the gills in response to soft-water conditions, and underscore the costs and limitations of soft-water acclimation. R. C. Playle—Deceased.     

Use of electromyogram telemetry to assess the behavioural and energetic responses of rainbow trout, Oncorhynchus mykiss (Walbaum) to transportation stress

Behavioural and energetic responses of domesticated rainbow trout Oncorhynchus mykiss (Walbaum) (mean fork length=440±45 mm) to a brief transportation episode were investigated. Fish implanted with radio transmitters measuring muscle activity (electromyogram; EMGi) were transported in a standard commercial shipping tank for 50 min by truck, and then allowed to recuperate for 48 h in stationary culture tanks. The EMGi telemetry data indicated that vigorous swimming activity occurred during transportation. Telemetry recordings also indicated that the fish's swimming activity returned to baseline levels within the 48 h period after transport. However, even beyond the 48 h resting period, the swimming performance (measured as critical speed and endurance) of transported fish was still impaired relative to non‐transported controls (P<0.05). Respirometry measurements of fish taken after transportation indicated that oxygen consumption (V_o2) was significantly elevated. The rise in V_o2 of post‐transport fish could be attributed to handling procedures, as well as the intense swimming behaviour observed during transportation. Therefore, the behavioural responses of fish during transportation produced physiological consequences that persisted long after the transportation event. This study demonstrates the potential for utilizing behavioural measures, in concert with biotelemetry technologies, as tools to assess the impacts of routine aquacultural procedures on the health and welfare of captive fish.     

Endurance of farmed and sea-ranched Atlantic salmon Salmo salar L. at spawning

Endurance of farmed and sea-ranched Atlantic salmon Salmo salar L. males was analysed during spawning time. The fish were endurance tested at different swimming speeds (1.6–2.1 m s^?1) in forced swim trials. The sea-ranched males (51-65 cm, n= 20) fatigued significantly earlier than the farmed males(59-72 cm, n= 20),although the sea-ranched males were significantly smaller than the farmed males. When the size difference between the two groups were corrected for, no significant difference in the endurance of the two groups was found. Farmed salmon had a significant higher fat content in white muscle (4.7%) than sea-ranched salmon (1.1%).     

Effects of Loma morhua (Microsporidia) infection on the cardiorespiratory performance of Atlantic cod Gadus morhua (L).

The microsporidian Loma morhua infects Atlantic cod (Gadus morhua) in the wild and in culture and results in the formation of xenomas within the gill filaments, heart and spleen. Given the importance of the two former organs to metabolic capacity and thermal tolerance, the cardiorespiratory performance of cod with a naturally acquired infection of Loma was measured during an acute temperature increase (2 °C h^?1) from 10 °C to the fish's critical thermal maximum (CT_Max). In addition, oxygen consumption and swimming performance were measured during two successive critical swimming speed (U_crit) tests at 10 °C. While Loma infection had a negative impact on cod cardiac function at warm temperatures, and on metabolic capacity in both the CT_Max and U_crit tests (i.e. a reduction of 30–40%), it appears that the Atlantic cod can largely compensate for these Loma‐induced cardiorespiratory limitations. For example, (i) CT_Max (21.0 ± 0.3 °C) and U_crit (~1.75 BL s^?1) were very comparable to those reported in previous studies using uninfected fish from the same founder population; and (ii) our data suggest that tissue oxygen extraction, and potentially the capacity for anaerobic metabolism, is enhanced in fish infected with this microsporidian.     

Fatigue analysis of the jack mackerel <Emphasis Type="Italic">Trachurus japonicus</Emphasis> by electrocardiographic monitoring during prolonged swimming

The effect of fatigue on swimming performance was examined by measuring the swimming endurance time and heart rate of the jack mackerel Trachurus japonicus [15.7 ± 0.8 cm fork length (FL), n = 15] during forced exercise in a flume tank at fixed swimming speeds of 4, 5 and 6 FL/s. Electrocardiographic (ECG) monitoring during the experimental process from control (0.8 FL/s) to exercise phase revealed a rapid cardiac response of T. japonicus to the elevation of swimming speed. The heart rate of T. japonicus significantly increased from the control level of 52.9 beats/min at a slow flow speed of 0.8 FL/s to 148.2 beats/min at 4 FL/s, 168.6 beats/min at 5 FL/s and 183.2 beats/min at 6 FL/s. During the fixed speed test, the heart rate of each individual fish was stabilized without any recognizable increase or decrease until the fish failed to swim because of fatigue. Fatigue analysis on endurance time demonstrated that prior swimming experience at prolonged speeds would impair the endurance performance during subsequent swimming exercise. Recovery time of the heart rate after the fish was fully exhausted by prolonged fast exercise increased with increasing swimming endurance time.     

Optimal swimming speeds reflect preferred swimming speeds of brook charr (<Emphasis Type="Italic">Salvelinus fontinalis</Emphasis> Mitchill, 1874)

Several measures have been developed to quantify swimming performance to understand various aspects of ecology and behaviour, as well as to help design functional applications for fishways and aquaculture. One of those measures, the optimal swimming speed, is the speed at which the cost of transport (COT) is minimal, where COT is defined as the cost of moving unit mass over unit distance. The experimental protocol to determine the optimal swimming speed involves forced-swimming in a flume or respirometer. In this study, a 4.5–m-long tilted raceway with gradually increasing upstream water speed is used to determine a novel, behaviourally based swimming parameter: the preferred swimming speed. The optimal swimming speed and the preferred swimming speed of brook charr were determined and a comparison of the two reveals that the optimal swimming speed (25.9 ± 4.5 cm s⁻¹ or 1.02 ± 0.47 bl s⁻¹) reflected the preferred swimming speed (between 20 cm s⁻¹ or 0.78 ± 0.02 bl s⁻¹ and 25 cm s⁻¹ or 0.95 ± 0.03 bl s⁻¹). The preferred swimming speed can be advantageous for the determination of swimming speeds for the use in aquaculture studies.     

The swimming capacity of juvenile Murray cod (Maccullochella peelii): an ambush predator endemic to the Murray‐Darling Basin,Australia

This study documented the swimming capacity of a large ambush predator, Murray cod Maccullochella peelii, endemic to the Murray‐Darling Basin, Australia. It was evident that the species is a swimming generalist, maintaining moderate ability across all aspects of the swimming capacity parameters that were investigated. For instance, the species was capable of prolonged swimming performance (critical swimming speed, U_crit: absolute, 0.26–0.60 m·s^?1, relative, 1.15–2.20 BL s^?1) that was inferior to active fish species, but comparable with other ambush predators. The species had low energetic demands, maintaining a low mass‐specific standard (21.3–140.3 mg·h^?1 kg^?1) and maximum active metabolic rate (75.5–563.8 mg·h^?1 kg^?1), which lead to a small scope for activity (maximum active metabolic rate–standard metabolic rate; 1.4–5.9). They were reasonably efficient swimmers (absolute and relative optimal swimming speed, 0.17–0.61 m·s^?1 and 0.77–1.93 BL·s^?1, respectively) and capable of repeat bouts of prolonged performance (recovery ratio = 0.99). Allometric changes in aspects of swimming capacity were realised with body mass, whereas broad swimming capacity was maintained across a wide range of temperatures. The swimming capacity demonstrated by M. peelii reflects a sit‐and‐wait foraging strategy that seeks to conserve energy characteristic of ambush predators, but with distinct features (e.g., lack of fast‐start ability) that may reflect their evolution in some of the world's most hydrologically and thermally variable rivers.     

Sex differences in metabolic rate and swimming performance in pink salmon (Oncorhynchus gorbuscha): the effect of male secondary sexual traits

Do secondary sexual traits, such as large dorsal hump and hooked snout, decrease the swimming efficiency of male pink salmon during freshwater migration? This is the first study to address the effects of secondary sexual traits in pink salmon on oxygen uptake and swimming capacity. We conducted a laboratory experiment using a swimming respirometer and a field study using electromyogram (EMG) telemetry in the Shibetsu River, Hokkaido, Japan. We compared the relationship between MO₂ (mg O₂·kg^?1·h^?1) and swimming velocity U (m·s^?1) in male and female fish, and also investigated the effects of morphological traits (secondary sexual characters) on the relationship between MO₂ (mg O₂·kg^?1·h^?1) and swimming velocity U (m·s^?1). Additionally, we compared energy costs and swimming behaviour during upstream migration between male and female pink salmon. The laboratory experiment revealed that MO₂ exponentially increased with increasing U; this increase was described by MO₂ = 167.9e^1.23U for males and 144.9e^1.14U for females. Linear mixed models found that hump height and the upper jaw length in males significantly and positively affected the relationship between MO₂ and U; no effect was found in females. The field study found that swimming velocity for both sexes estimated from EMG calibration was lower than optimal swimming velocity (U_opt) calculated from the laboratory experiment. We suggest that pink salmon in the Shibetsu River do not swim at the optimal swimming velocity because of the short migration distance involved (20 km).     

Dietary arginine requirement of fingerling hybrid Clarias (Clarias gariepinus×Clarias macrocephalus)

The dietary arginine requirement of fingerling hybrid Clarias (Clarias gariepinus×Clarias macrocephalus) (4.2±0.03 cm, 0.56±0.04 g) was determined by feeding six isonitrogenous (400 g kg⁻¹ crude protein) and isocaloric (17.9 kJ g⁻¹) amino acid test diets containing casein, gelatin and l ‐crystalline amino acids with graded levels of arginine (10.0, 12.5, 15.0, 17.5, 20.0 and 22.5 g kg⁻¹) for 4 weeks to triplicate groups. Diets were fed twice a day at 09:00 and 16:00 hours at 8% body weight day⁻¹. Maximum weight gain (523%), best feed conversion ratio (FCR, 1.41), protein efficiency ratio (1.78) and specific growth rate (6.53%) were recorded in fish fed the diet containing arginine at 20.0gkg⁻¹ of the diet. Second‐degree polynomial regression analysis of live weight gain and FCR values indicated the dietary arginine requirement at 17.8 and 20.0 g kg⁻¹ of dry diet respectively. Significantly higher carcass protein and protein deposition values were recorded at the requirement level (20.0 g kg⁻¹). Higher fat and lower moisture values were obtained in carcass of fish fed the diet with 15.0g kg⁻¹ arginine. The maximum carcass ash value was noticed in the fish fed at 20.0 g kg⁻¹ dietary arginine. We recommend that the diet for hybrid Clarias (C. gariepinus×C. macrocephalus) should contain arginine in the range of 17.8–20.0 g kg⁻¹ of the dry diet, corresponding to 44.5 and 50 g kg⁻¹ of dietary protein respectively.     

Effect of stocking density,oxygen level,light regime and swimming velocity on the incidence of sexual maturation in adult Atlantic salmon (Salmo salar)

The effects of various environmental parameters on sexual maturation of two sea-winter Atlantic salmon (Salmo salar) were tested in two separate experiments. In the first experiment Atlantic salmon with initial mean individual weight 1.5 kg (smolt 13 months before) were reared for 8 months from June to February at different oxygen levels and stocking densities using continuous light. Oxygen levels of 5–7, 7.5–9.5 and 10–12 mg O₂ l⁻¹ and stocking densities starting at about 20, 30 and 40 kg m⁻³ and increasing as the fish grew to 80–90 kg m⁻³ for the highest densities were tested in a factorial design. Only male fish matured, and incidence of maturation among males varied from 4.1% to 25% between tanks. The highest percentage of mature males was found in the tanks with low stocking density. No clear effect on oxygen level was found.The second experiment lasted 20 months from seawater transfer in May until the fish weighed 3.3–3.5 kg. Two water current speeds (14–16 and 20–24 cm s⁻¹) and two photoperiod regimes (LD 20:4) and continuous light (LL) were tested in a factorial design. Neither swimming velocity nor photoperiod affected growth rate. Continuous light reduced the incidence of sexual maturation. The average proportion of maturation among males was 8% and 25% under the LL and LD 20:4 regimes respectively. The fish reared under the LD 20:4 light regime had a significant lower condition factor and significant larger hearts than the fish reared under continuous light. Swimming velocity had no significant effect on the incidence of maturation. The results indicate that the swimming velocity must be higher than 0.5 BL s⁻¹ in order to influence the energy stores. An important finding in this study is that light cues are not required for gonadal growth. The results also indicate that environmental factors can affect maturation even after the first sea-winter.     

Effects of stocking density on growth, yield and profitability of farming Nile tilapia, Oreochromis niloticus L., fed Azolla diet, in earthen ponds

Two consecutive experiments were conducted to study the effects of stocking density on growth, food utilization, production and farming profitability of Nile tilapia (Oreochromis niloticus) fingerlings (initial mean weight: 16.2 ± 0.2 g) fed Azolla, as a main component in diet. In experiment 1, fish were hand‐fed twice daily with three isonitrogenous (28.5% crude protein) and isocaloric (14.5 kJ g⁻¹) diets A30, A35 and A40 containing 30%, 35% and 40%Azolla, respectively, for 90 days. Diets were formulated by mixing Azolla with locally available by‐products. No significant differences were found in growth parameters and production (P>0.05). Total investment cost was significantly higher with A30 (P<0.05), but same profitability values were obtained with all diets (P>0.05). In experiment 2, three stocking densities, 1, 3 and 5 m⁻², were assigned to three treatments T₁, T₂ and T₃ respectively. Fish were hand‐fed twice daily with diet A40. The final mean weight (89.53–115.12 g), the mean weight gain (0.81–1.10 g day⁻¹), the specific growth rate (1.90–2.20% day⁻¹) and the apparent food conversion ratio (1.29–1.58) were affected by stocking density, with significant difference (P<0.05) at 5 m⁻², compared with the other densities. Stocking density did not affect survival rate (P>0.05). Yield and annual production increased with increasing stocking density, ranging from 7.10 ± 0.90 to 25.01 ± 1.84 kg are⁻¹ and 28.79 ± 3.66 to 101.42 ± 7.48 kg are⁻¹ year⁻¹, respectively, with significant differences between all densities (P<0.05). Higher stocking density resulted in higher gross return and lower cost of fish production, with significant variations (P<0.05). The net return increased with increasing stocking density (P<0.05). However, both densities of 3 and 5 m⁻² produced the same profitability values. On the basis of growth values and economic return, it was concluded that Nile tilapia could be raised at a density of 3 fish m⁻² with A40 to improve production and generate profit for nutritional security and poverty alleviation in rural areas.     

Differences in swimming performance and energetic costs between an endangered native toothcarp (Aphanius iberus) and an invasive mosquitofish (Gambusia holbrooki)

Swimming performance is a key feature that mediates fitness and survival in many fish species. Using a swim tunnel respirometer, we compared prolonged swimming performance and energy use for two competing species: an endangered, endemic toothcarp (Aphanius iberus) and a worldwide invasive mosquitofish (Gambusia holbrooki). Critical (U_crit) and optimal swimming speeds, standard and maximal metabolic rates, absolute aerobic scope, as well as the minimum cost of transport were estimated and compared between species and sexes. Body streamlining and caudal peduncle depth were also measured to explain the differences in swimming performance and efficiency. Both sexes of A. iberus presented similar swimming capacity and metabolic traits, whereas males of G. holbrooki showed higher critical swimming speeds, maximal metabolic rate and absolute aerobic scope than females. We also found marked differences between species in most of the response variables examined. Aphanius iberus showed lower swimming capacity (U_crit mean <10 cm s⁻¹), higher maximal metabolic rate and absolute aerobic scope than the invasive species. By contrast, G holbrooki swam faster and had lower cost of transport at a given fish mass and speed, thereby leading to a higher swimming efficiency. The observed differences in swimming efficiency were closely related to differences in morphological characteristics and therefore to drag pressures and propulsion. Our results add a mechanistic basis to the ecological understanding of these two species and suggest that although both are poor swimmers compared to many other similarly sized species, the native species likely has more restricted water flow tolerance and dispersal capacities.     

Influence of feeding regime on intraspecific competition, fin damage and growth in 1+ Atlantic salmon parr (Salmo salar L.) held in freshwater production cages

The feeding behaviour, growth and feed conversion ratio (FCR) of cage‐held Atlantic salmon parr (Salmo salar L.) were studied when in 576 m³ (12 m × 12 m × 4 m) commercial freshwater cages under ambient water temperature (8.84±3.53°C) and photoperiod (11.02±2.05 h) for 205 days. The effect of feeding regime on fin damage was also investigated. Six groups (n=31 234±2051 fish group⁻¹, initial stocking density 1.25±0.14 kg m⁻³) were fed to satiation using either (a) an imposed regime involving scheduled, fixed ration feeding every 10 min from dawn till dusk or (b) on demand from dawn till dusk using commercial interactive feedback systems. During feeding, there were no significant differences in aggression although swimming speeds and turning angles were significantly higher in fish under the imposed regime. On‐demand feeding significantly reduced the incidence of dorsal fin damage. There was no clear relationship between fish size, feed regime and the incidence of fin damage until 1 week before the fish were transferred to marine cages, when the smallest fish under each feeding regime had the highest incidence of fin damage. Interestingly, growth did not differ between regimes, but fish under the imposed regime were significantly overfed and achieved higher FCRs.     

Effects of size and sex on swimming performance and metabolism of invasive mosquitofish Gambusia holbrooki

In freshwater ecosystems, abiotic factors such as flow regime and water quality are considered important predictors of ecosystem invasibility. The aim of this study was to investigate the critical swimming capacity and metabolism of the eastern mosquitofish, Gambusia holbrooki, focusing on sex and size effects, to evaluate the influence of water flow on its invasive success. Specimens of mosquitofish were captured from the Ter Vell lagoon (L'Estartit, north‐eastern Spain) in July 2014, and we measured the critical swimming speed (U_crit) and oxygen consumption of individual fish (30 females and 30 males) using a mini swim tunnel. The mean U_crit of this poeciliid fish was estimated at 14.11 cm·s^?1 (range = 4.85–22.26), which is lower than that of many other fishes of similar size and confirms that this species is limnophilic and its invasive success might be partially explained by hydrologic alterations. However, the U_crit and maximal metabolic rate vary markedly with fish size and sex, with males having much higher values for the same body mass, and thus probably being more resistant to strong water flows. Multiple regression models illustrate that multivariate analyses might increase the predictive power and understanding of swimming performance and metabolic traits, compared to results from conventional simple regressions.     

Effects of pectoral fin ray removal on Siberian sturgeon <Emphasis Type="Italic">Acipenser baerii</Emphasis> swimming performance

Fin ray biopsies are commonly used to age sturgeon, but the effects of fin ray biopsy on Siberian sturgeon Acipenser baerii swimming performance are unknown. Therefore, the effects of two fin ray biopsy methods on swimming performance of hatchery-reared, juvenile Siberian sturgeon were evaluated in this study. Treatment fish were subjected to one of two biopsy methods: removal of a 2- to 4-cm section from a marginal pectoral fin ray, or full removal of a marginal pectoral fin ray. Control fish were only subjected to a sham operation. A modified 2,936-l Brett-type swim tunnel was used to evaluate 10-min critical station-holding speeds (C _SHS) and behavioral swimming characteristics of sturgeon immediately after fin ray biopsies were carried out. Fish sizes (range 65- to 84-cm fork length) were comparable among treatments. Mean 10-min C _SHS (mean ± SE) were 113 ± 3.4, 109 ± 2.5, and 111 ± 2.8 cm s^?1 for the segment removal treatment, full removal treatment, and control treatment, respectively. ANOVA indicated that the two methods had no significant effect on the 10-min C _SHS of Siberian sturgeon compared to the control treatment. Results indicate that fin ray removal has no effect on Siberian sturgeon swimming performance.     

Swimming angle and target strength of larval Japanese anchovy (<Emphasis Type="Italic">Engraulis japonicus</Emphasis>)

The swimming angle of larval Japanese anchovy (Engraulis japonicus) was measured in a tank, and target strength (TS) was calculated using a theoretical scattering model. The mean swimming angle was 12.8° (SD ±22.1). Increased speeds of flow led to increased mean swimming angles. The mean swimming angle at flow of 5 cm s⁻¹ was higher than at other speeds. TS values were estimated using a distorted-wave Born approximation model for two cases. Average values were 1–3 cm s⁻¹ (11.5° ± 22.1) and 5 cm s⁻¹ (16.6° ± 21.7) for cases 1 and 2, respectively. For case 1, TS ranged from −92.0 to −74.7 dB with a mean of −79.4 dB at 120 kHz. For case 2, TS ranged from −92.2 to −75.2 dB with a mean of −79.9 dB. The mean TS in case 2 was lower than that in case 1, with the maximum difference being 1.0 dB at 120 kHz (standard length 22.0 mm). However, there were no significant differences between the regression lines of cases 1 and 2. Thus, changes in flow speed altered the swimming angle of larval Japanese anchovy, but had little influence on TS.     

Effect of temperature on the swimming endurance and post-exercise recovery of jack mackerel <Emphasis Type="Italic">Trachurus japonicus</Emphasis> as determined by ECG monitoring

The effect of temperature on the swimming performance of jack mackerel Trachurus japonicus was examined in a flume tank by measuring the swimming endurance time and heart rate. The lower swimming performance was observed at 10°C (the lowest temperature tested), manifesting as the shortest endurance time and the slowest maximum sustained speed. ECG measurements of the heart rate under free-swimming conditions at zero flow velocity revealed a temperature effect, with 25.3 beats/min observed at 10°C, 38.9 at 15°C, and 67.2 at 22°C. The heart rate also increased with swimming speed to maximum levels of 60, 125, and 208 beats/min, respectively, at these three temperatures. Heart rate recovery times measured after the fish had been swimming at prolonged speed tended to increase with temperature, while a negative correlation resulting in relatively short recovery times was observed after swimming at close to the burst swimming speed at each water temperature.