Effect of thermo-velocity barriers on fish: influence of water temperature,flow velocity and body size on the volitional swimming capacity of northern straight-mouth nase (Pseudochondrostoma duriense)

Water temperature and flow velocity directly affect the fish swimming capacity, and thus, both variables influence the fish passage through river barriers. Nonetheless, their effects are usually disregarded in fishway engineering and management. This study aims to evaluate the volitional swimming capacity of the northern straight-mouth nase (Pseudochondrostoma duriense), considering the possible effects of water temperature, flow velocity and body size. For this, the maximum distance, swim speed and fatigue time (FT) were studied in an outdoor open-channel flume in the Duero River (Burgos, Spain) against three nominal velocities (1.5, 2.5 and 3 m s⁻¹) and temperatures (5.5, 13.5 and 18.5°C), also including the changes between swimming modes (prolonged and sprint). Results showed that a nase of 20.8 cm mean fork length can develop a median swim speed that exceeds 20.7 BL s⁻¹ (4.31 m s⁻¹) during a median time of 3.4 s in sprint mode, or 12.2 BL s⁻¹ (2.55 m s⁻¹) for 23.7 s in prolonged mode under the warmest scenario. During prolonged swimming mode, fish were able to reach further distances in warmer water conditions for all situations, due to a greater swimming speed and FT, whereas during sprint mode, warmer conditions increased the swim speed maintaining the FT. In conclusion, the studied temperature range and flow velocity range influence fish swimming performance, endurance and distance travelled, although with some differences depending on the swimming mode. The provided information goes a step forward in the definition of real fish swimming capacities, and in turn, will contribute to establish clear passage criteria for thermo-velocity barriers, allowing the calculation of the proportion of fish able to pass a barrier under different working scenarios, as well designing of the optimized solutions to improve the fish passage through river barriers.     

Investigating a major assumption of predictive instream habitat models: is water velocity preference of juvenile Atlantic salmon independent of discharge?

The mean column velocity preference of juvenile Atlantic salmon Salmo salar (LF 30–55 mm) was investigated by observing their spatial pattern of habitat use in a laboratory flume while varying discharge (Q) over a 18‐fold range (Q=2·6–46·8l s^‐1). Based on 341 fish observations at three discharges (Q=2·6, 15·0 and 46·8l s^‐1), three separate velocity preference curves were developed using standard procedures. The mean column velocities measured at 0·6 depth for the fish positions at the set low, medium and high discharges had medians of 7, 10 and 24 cm s^‐1, respectively, and varied significantly between the discharges. Across the range of flows, the fish utilized mean column velocities between 0 and 56 cm s^‐1, but the three velocity preference curves differed. Differences between juvenile Atlantic salmon use of habitat, defined according to mean column velocities at different discharges, were greatest at the lower end of the available range of velocities (<20 cm s^‐1). Weighted usable area (WUA), the output of the instream flow model PHABSIM that is used to describe the available habitat at a given discharge, was calculated for the flume using the preference curves built at the three set discharges. The model was highly sensitive to differences between the three preference curves and WUA varied by up to a two‐fold difference. Furthermore, habitat‐discharge relationships derived from the three preference curves were very different. Predicted habitat losses across the modelled range of discharges varied by up to 150% depending upon which velocity preference curve was used in the model. Thus, the assumption that a single preference curve can be applied across a range of discharges is not valid and is likely to result in large errors when employing PHABSIM and other models that use similar principles.     

Differences in the energetic cost of swimming in turbulent flow between wild,farmed and domesticated juvenile Atlantic salmon Salmo salar

Domestication has been shown to have an effect on morphology and behaviour of Atlantic salmon (Salmo salar). We compared swimming costs of three groups of juvenile Atlantic salmon subject to different levels of domestication: (1) wild fish; (2) first generation farmed fish origination from wild genitors; and (2) seventh generation farmed fish originating from Norwegian aquaculture stocks. We assessed swimming costs under two types of turbulent flow (one mean flow velocity of 23 cm s^?1 and two standard deviations of flow velocity of 5 and 8 cm s^?1). Respirometry experiments were conducted with fish in a mass range of 5–15 g wet at a water temperature of 15° C. Our results confirm (1) that net swimming costs are affected by different levels of turbulence such that, for a given mean flow velocity, fish spent 1·5‐times more energy as turbulence increased, (2) that domesticated fish differed in their morphology (having deeper bodies and smaller fins) and in their net swimming costs (being up to 30·3% higher than for wild fish) and (3) that swimming cost models developed for farmed fish may be also be applied to wild fish in turbulent environments.     

Effects of surgically implanted acoustic transmitters >2% of body mass on the swimming performance, survival and growth of juvenile sockeye and Chinook salmon

The influence of surgical implantation of an acoustic transmitter on the swimming performance, growth and survival of juvenile sockeye salmon Oncorhynchus nerka and Chinook salmon Oncorhynchus tshawytscha was examined. The transmitter had a mass of 0·7 g in air while sockeye salmon had a mass of 7·0–16·0 g and Chinook salmon had a mass of 6·7–23·1 g (a transmitter burden of 4·5–10·3% for sockeye salmon and 3·1–10·7% for Chinook salmon). Mean critical swimming speeds (U_crit) for Chinook salmon ranged from 47·5 to 51·2 cm s^?1 [4·34–4·69 body lengths (fork length, L_F) s^?1] and did not differ among tagged, untagged and sham‐tagged groups. Tagged sockeye salmon, however, did have lower U_crit than control or sham fish. The mean U_crit for tagged sockeye salmon was 46·1 cm s^?1 (4·1 L_F s^?1), which was c. 5% less than the mean U_crit for control and sham fish (both groups were 48·6 cm s^?1 or 4·3 L_F s^?1). A laboratory evaluation determined that there was no difference in L_F or mass among treatments (control, sham or tag) either at the start or at the end of the test period, suggesting that implantation did not negatively influence the growth of either species. None of the sockeye salmon held under laboratory conditions died from the influence of surgical implantation of transmitters. In contrast, this study found that the 21 day survival differed between tagged and control groups of Chinook salmon, although this result may have been confounded by the poor health of Chinook salmon treatment groups.     

Maximum sustainable speed, energetics and swimming kinematics of a tropical carangid fish, the green jack Caranx caballus

Maximum sustained swimming speeds, swimming energetics and swimming kinematics were measured in the green jack Caranx caballus (Teleostei: Carangidae) using a 41 l temperature‐controlled, Brett‐type swimming‐tunnel respirometer. In individual C. caballus [mean ±s.d. of 22·1 ± 2·2 cm fork length (L_F), 190 ± 61 g, n = 11] at 27·2 ± 0·7° C, mean critical speed (U_crit) was 102·5 ± 13·7 cm s^?1 or 4·6 ± 0·9 L_F s^?1. The maximum speed that was maintained for a 30 min period while swimming steadily using the slow, oxidative locomotor muscle (U_max,c) was 99·4 ± 14·4 cm s^?1 or 4·5 ± 0·9 L_F s^?1. Oxygen consumption rate (M in mg O₂ min^?1) increased with swimming speed and with fish mass, but mass‐specific M (mg O₂ kg^?1 h^?1) as a function of relative speed (L_F s^?1) did not vary significantly with fish size. Mean standard metabolic rate (R_S) was 170 ± 38 mg O₂ kg^?1 h^?1, and the mean ratio of M at U_max,c to R_S, an estimate of factorial aerobic scope, was 3·6 ± 1·0. The optimal speed (U_opt), at which the gross cost of transport was a minimum of 2·14 J kg^?1 m^?1, was 3·8 L_F s^?1. In a subset of the fish studied (19·7–22·7 cm L_F, 106–164 g, n = 5), the swimming kinematic variables of tailbeat frequency, yaw and stride length all increased significantly with swimming speed but not fish size, whereas tailbeat amplitude varied significantly with speed, fish mass and L_F. The mean propulsive wavelength was 86·7 ± 5·6 %L_F or 73·7 ± 5·2 %L_T. Mean ±s.d . yaw and tailbeat amplitude values, calculated from lateral displacement of each intervertebral joint during a complete tailbeat cycle in three C. caballus (19·7, 21·6 and 22·7 cm L_F; 23·4, 25·3 and 26·4 cm L_T), were 4·6 ± 0·1 and 17·1 ± 2·2 %L_T, respectively. Overall, the sustained swimming performance, energetics, kinematics, lateral displacement and intervertebral bending angles measured in C. caballus were similar to those of other active ectothermic fishes that have been studied, and C. caballus was more similar to the chub mackerel Scomber japonicus than to the kawakawa tuna Euthynnus affinis.     

Resisting flow–laboratory study of rheotaxis of the estuarine copepod Pseudodiaptomus annandalei

Rheotaxis is a ubiquitous phenomenon among aquatic animals and thought to be an adaptation to maintain populations in flowing waters. While many estuarine copepods can retain their populations in estuaries with net seaward flow, rheotaxis of individual copepods has not been reported before. In this study, the behavior of a calanoid copepod Pseudodiaptomus annandalei in flow was examined in a recirculating laboratory flume. This estuarine copepod displayed different responses to ambient flow fields while swimming in the water column or attaching to the flume bed (walls). Copepods in the water column showed vigorous countercurrent swimming by occasional bounding when flow velocity was increased up to 2.1 cm s^?1, but none of the individuals in the water column were retained in the flume when flow speeds were higher than 4 cm s^?1. This indicates P. annandalei profits little from rheotaxis to withstand flow when they were swimming in the water column. Instead, more individuals attempted sinking downwards to the slow flow region near the flume bed (walls) and showed active substrate attachment to avoid being flushed out by the high-velocity channel flow. The results suggest that P. annandalei benefits from rheotaxis and association with the substrate which allows them to hold position well at ambient flow velocities up to 3 cm s^?1. These adaptive responses might be important for population maintenance.     

Ontogeny of critical and prolonged swimming performance for the larvae of six Australian freshwater fish species

Critical (<30 min) and prolonged (>60 min) swimming speeds in laboratory chambers were determined for larvae of six species of Australian freshwater fishes: trout cod Maccullochella macquariensis, Murray cod Maccullochella peelii, golden perch Macquaria ambigua, silver perch Bidyanus bidyanus, carp gudgeon Hypseleotris spp. and Murray River rainbowfish Melanotaenia fluviatilis. Developmental stage (preflexion, flexion, postflexion and metalarva) better explained swimming ability than did length, size or age (days after hatch). Critical speed increased with larval development, and metalarvae were the fastest swimmers for all species. Maccullochella macquariensis larvae had the highest critical [maximum absolute 46·4 cm s^?1 and 44·6 relative body lengths (L_B) s^?1] and prolonged (maximum 15·4 cm s^?1, 15·6 L_B s^?1) swimming speeds and B. bidyanus larvae the lowest critical (minimum 0·1 cm s^?1, 0·3 L_B s^?1) and prolonged swimming speeds (minimum 1·1 cm s^?1, 1·0 L_B s^?1). Prolonged swimming trials determined that the larvae of some species could not swim for 60 min at any speed, whereas the larvae of the best swimming species, M. macquariensis, could swim for 60 min at 44% of the critical speed. The swimming performance of species with precocial life‐history strategies, with well‐developed larvae at hatch, was comparatively better and potentially had greater ability to influence their dispersal by actively swimming than species with altricial life‐history strategies, with poorly developed larvae at hatch.     

Effects of age and size on critical swimming speed of juvenile Chinese sturgeon Acipenser sinensis at seasonal temperatures

Changes in the critical swimming speed (U_crit, cm s^?1) with ontogeny of 2·5–12·5 month‐old juvenile anadromous Chinese sturgeon Acipenser sinesis were measured in a modified Blazka‐type swimming tunnel. The absolute U_crit increased with length, mass and age; the relative U^′_crit (body lengths, s^?1), however, decreased. Juvenile A. sinesis did not display a parr–smolt transformation at the length or age threshold to tolerate full‐strength seawater.     

Displacement,velocity preference,and substrate use of three native California stream fishes in simulated pulsed flows

We studied whether juvenile fishes were able to maintain swimming speed and position during simulated river pulsed flows in a laboratory flume. We used a glass flume (15.24 × 0.6 m) with river-rock substrate to determine the longitudinal displacement, movement distances and frequencies, velocity selection, and substrate use of juvenile (SL range: 6.1 ± 0.2 cm) hardhead Mylopharodon conocephalus (n = 13), rainbow trout Oncorhynchus mykiss (n = 11), and Sacramento sucker Catostomus occidentalis (n = 12) during a 100-min flow pulse, as velocity changed from slow to medium, fast, medium, and slow. Fish were capable of maintaining swimming speed and position up to the maximum flume velocity of 0.46 m·s⁻¹, except for one hardhead that impinged on the rear fish screen. Fish swam faster in the flume during the medium and fast intervals than the slow intervals, but fish speeds were similar among the medium and faster intervals, when some fish took cover behind the rock substrate. In comparison with a Brett-type swim-tunnel, fish showed less increase in mean swimming speed as the flume velocity increased. Fish in the flume were able to use the rock substrate as hydraulic cover, decreasing the encountered water velocity, and, presumably, conserving energy.     

The effect of substratum type on aspects of swimming performance and behaviour in shortnose sturgeon Acipenser brevirostrum

The swimming performance and associated swimming behaviour (i.e. substratum‐skimming, station‐holding and free swimming) were assessed in shortnose sturgeon Acipenser brevirostrum during critical swimming and endurance swimming tests over a rough and a smooth substratum. It was hypothesized that the addition of a rough substratum in the swimming flume may provide a surface for the A. brevirostrum to grip and offer an energetic advantage. Substratum type did not affect the critical swimming performance, but A. brevirostrum consistently performed more bottom behaviours (i.e. substratum‐skimming and station‐holding) while on a smooth substratum. Acipenser brevirostrum had little contact with the rough substratum until the velocity was >1 body length s^?1. Endurance swimming time was significantly lower for A. brevirostrum over the rough bottom at the highest velocity (30 cm s^?1) which may be attributed to the observed increase in free swimming and decrease in bottom behaviours. During endurance swimming, the rough substratum was mainly used at intermediate velocities, suggesting that there may be a stability cost associated with being in contact with the rough substratum at certain velocities.     

Effect of two flow regimes on the upstream movements of the Iberian barbel (Luciobarbus bocagei) in an experimental pool‐type fishway

Literature related to pool‐type fishways has seen a recent upsurge of interest in the placement of instream structures for improving fish passage. However, there is still no information on how different flow regimes created by boulder placement have an influence on upstream fish movements. The main goal of this study was to assess the performance of two different flow regimes, characterized by the relative depth of flow (d/h), where d is the water depth and h is the height of artificial bottom substrata, in assisting fish passage in an experimental full‐scale pool‐type fishway. Two series of experiments consisting of 20 replicates each and representing distinct flow regimes created by boulder placement in the flume bottom – d/h > 4 (regime 1) and 1.3 < d/h < 4 (regime 2) – were carried out to analyse the proportion and timing of successful upstream movements of a potamodromous cyprinid, the Iberian barbel (Luciobarbus bocagei). Although no significant differences (P > 0.05) in passage success were observed between regimes (55% and 60%, respectively), fish transit time was significantly lower (P < 0.05) in regime 2 (mean ± SD: 2.6 ± 1.6 min.) than in regime 1 (7.1 ± 5.8 min.). The results of these experiments show that lower relative depths can be more beneficial to fish passage because they reduce the transit time for successful negotiation, thus providing a useful indication on how to improve fish passage through pool‐type fishways.     

Phylogeography of Rhinichthys cataractae (Teleostei: Cyprinidae): pre‐glacial colonization across the Continental Divide and Pleistocene diversification within the Rio Grande drainage

The longnose dace, Rhinichthys cataractae, is a primary freshwater fish inhabiting riffle habitats in small headwater rivers and streams across the North American continent, including drainages east and west of the Continental Divide. The mitochondrially encoded cytochrome b gene (1140 bp) and 2298–2346 bp of the nuclear‐encoded genes S7 and RAG1 were obtained from 87 individuals of R. cataractae (collected from 17 sites throughout its range) and from several close relatives. Phylogenetic analyses recovered a monophyletic R. cataractae species‐group that contained Rhinichthys evermanni, Rhinichthys sp. ‘Millicoma dace’, and a non‐exclusive R. cataractae. Within the R. cataractae species‐group, two well‐supported lineages were identified, including a western lineage (containing R. evermanni, R. sp. ‘Millicoma dace’ and individuals of R. cataractae from Pacific slope drainages) and an eastern lineage (containing individuals of R. cataractae from Arctic, Atlantic, and Gulf slope drainages). Within the eastern lineage of R. cataractae, two well‐supported groups were recovered: a south‐eastern group, containing individuals from the Atlantic slope, southern tributaries to the Mississippi River, and the Rio Grande drainage; and a north‐eastern group, containing individuals from the Arctic slope and northern tributaries to the Mississippi River. Estimates of the timing of divergence within the R. cataractae species‐group, combined with ancestral area‐reconstruction methods, indicate a separation between the eastern and western lineages during the Pliocene to early‐Pleistocene, with a direction of colonization from the west of the Continental Divide eastward. Within the southern portion of its range, R. cataractae likely entered the Rio Grande drainage during the Pleistocene via stream capture events between the Arkansas River (Mississippi River drainage) and headwaters of the Rio Grande. A close relationship between populations of R. cataractae in the Rio Grande drainage and the adjacent Canadian River (Mississippi River drainage) is consistent with hypothesized stream capture events between the Pecos (Rio Grande drainage) and Canadian rivers during the late‐Pleistocene. The population of R. cataractae in the lower Rio Grande may have become separated from other populations in the Rio Grande drainage (upper Rio Grande and Pecos River) and Canadian River during the late‐Pleistocene, well before initiation of recent and significant anthropogenic disturbance within the Rio Grande drainage. © 2014 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 111 , 317–333.     

FLOW‐INDUCED MORPHOLOGICAL VARIATIONS AFFECT DIFFUSION BOUNDARY‐LAYER THICKNESS OF MACROCYSTIS PYRIFERA (HETEROKONTOPHYTA,LAMINARIALES)1

In slow mainstream flows (<4–6 cm · s^?1), the transport of dissolved nutrients to seaweed blade surfaces is reduced due to the formation of thicker diffusion boundary layers (DBLs). The blade morphology of Macrocystis pyrifera (L.) C. Agardh varies with the hydrodynamic environment in which it grows; wave‐exposed blades are narrow and thick with small surface corrugations (1 mm tall), whereas wave‐sheltered blades are wider and thinner with large (2–5 cm) edge undulations. Within the surface corrugations of wave‐exposed blades, the DBL thickness, measured using an O₂ micro‐optode, ranged from 0.67 to 0.80 mm and did not vary with mainstream velocities between 0.8 and 4.5 cm · s^?1. At the corrugation apex, DBL thickness decreased with increasing seawater velocity, from 0.4 mm at 0.8 cm · s^?1 to being undetectable at 4.5 cm · s^?1. Results show how the wave‐exposed blades trap fluid within the corrugations at their surface. For wave‐sheltered blades at 0.8 cm · s^?1, a DBL thickness of 0.73 ± 0.31 mm within the edge undulation was 10‐fold greater than at the undulation apex, while at 2.1 cm · s^?1, DBL thicknesses were similar at <0.07 mm. Relative turbulence intensity was measured using an acoustic Doppler velocimeter (ADV), and overall, there was little evidence to support our hypothesis that the edge undulations of wave‐sheltered blades increased turbulence intensity compared to wave‐exposed blades. We discuss the positive and negative effects of thick DBLs at seaweed surfaces.     

鲢幼鱼通过水流速度障碍的模拟

鱼类能否通过水流速度障碍直接影响过鱼设施的过鱼效果。利用计算机技术,综合水力因素、鱼类行为、地理特征及环境因子,展开鱼类通过水流速度障碍的模拟,有助于过鱼设施的优化设计。以国外涵洞式鱼道模拟软件Fish Xing为切入点,结合主要模块和关键因子,对我国特有鱼类鲢幼鱼进行模拟,得到鲢通过不同水流速度障碍的成功率;对比鲢在物理模型中的游泳表现,从模型主要模块和影响鱼类游泳表现的关键因子角度,分析影响鱼类通过水流速度障碍模拟的因素。结果表明,Fish Xing软件不能精确模拟鲢通过水流速度障碍的表现。分析表明,该软件在地理要素、管道特征和水力信息等参数方面具备独特的优势,但对我国鱼类有一定局限性,主要体现在鱼类的生物学信息如鱼类游泳特征等方面存在不足;进行鱼过障碍的模拟需要深入研究目标鱼类的生理特征、游泳能力及其与水力环境因子的响应关系。     

The critical swimming speed of Iberian barbel Barbus bocagei in relation to size and sex

The swimming capacity of Barbus bocagei was measured with the critical swimming speed (U_crit) standard test in a modified Bla?ka‐type swim tunnel. Sixty B. bocagei were tested and they exhibited a mean ±s .d . U_crit of 0·81 ± 0·11 m s^?1 or 3·1 ± 0·86 total lengths per second (L_T s^?1). Sex had no effect on U_crit but significant differences were found between the swimming performance of fish with distinct sizes.     

Heart rate as an indicator of metabolic rate and activity in adult Atlantic salmon, Salmo salar

Telemetered heart rate (f_H) was examined as an indicator of activity and oxygen consumption rate (VO₂) in adult, cultivated, Atlantic salmon, Salmo salar L. Heart rate was measured during sustained swimming in a flume for six fish at 10° C [mean weight, 1114 g; mean fork length (f. l.), 50·6 cm] and seven fish at 15° C (mean weight, 1119 g; mean f. l., 50·7 cm) at speeds of up to 2·2 body lengths/s. Semi–logarithmic relationships between heart rate and swimming speed were obtained at both temperatures. Spontaneously swimming fish in still water exhibited characteristic heart rate increases associated with activity. Heart rate and Vo₂ were monitored simultaneously in a 575–1 circular respirometer for six fish (three male, three female) at 4° C (mean weight, 1804 g; mean F. L., 62· cm) and six fish (three male, three female) at 10° C (mean weight, 2045 g; mean f. l., 63·2 cm) during spontaneous but unquantified activity. Linear regressions were obtained by transforming data for both f_H and Vo₂ to log values. At each temperature, slopes of the regressions between f_H and Vo₂ for individual fishes were not significantly different, but in some cases elevations were. All differences in elevation were between male and female fish. There were no significant differences in regression slope or elevation for fish of the same sex at the two temperatures and so regressions were calculated for the sexes, pooling data from 4 and 10° C. There was no significant difference in the mean ± S. D. Vo₂ between the sexes at 4° C (male, 66·0 ± 59·6 mgO₂ kg^?1 h^?1; female, 88·0 ± 60·1 mgO₂ kg^?1 h^?1) or 10° C (male, 166·2 ± 115·4 mgO₂ kg^?1 h^?1; female, 169·2 ± 111–1 mgO₂ kg^?1h^?1). Resting Vo₂ (x?± s. d.) at 4°C was 36·7 ± 8.4 mgO₂ kg^?1 h^?1, and 10° C was 72·8 ± 11·9 mgO₂ kg^?1 h^?1. Maximum Vo₂ (x?± S. D.) at 4° C was 250·6 ± 40·2 mgO₂ kg^?1 h^?1, and at 10° C was 423·6 ± 25·2 mgO₂ kg^?1 h^?1. Heart rate appears to be a useful indicator of metabolic rate over the temperature range examined, for the cultivated fish studied, but it is possible that the relationship for wild fish may differ.     

Aerobic scope for activity in age 0 year Atlantic cod Gadus morhua

Key components of swimming metabolism: standard metabolism (R_s), active metabolism (R_a) and absolute aerobic scope for activity (R_a–R_s) were determined for small age 0 year Atlantic cod Gadus morhua. Gadus morhua juveniles grew from 0·50 to 2·89 g wet body mass (M_WB) over the experimental period of 100 days, and growth rates (G) ranged from 1·4 to 2·9% day^?1, which decreased with increasing size. Metabolic rates were recorded by measuring changes in oxygen consumption over time at different activity levels using modified Brett‐type respirometers designed to accommodate the small size and short swimming endurance of small fishes. Power performance relationships were established between oxygen consumption and swimming speed measurements were repeated for individual fish as each fish grew. Mass‐specific standard metabolic rates () were calculated from the power performance relationships by extrapolating to zero swimming speed and decreased from 7·00 to 5·77 μmol O₂ g^?1 h^?1, mass‐specific active metabolic rates () were calculated from extrapolation to maximum swimming speed (U_max) and decreased from 26·18 to 14·35 μmol O₂ g^?1 h^?1 and mass‐specific absolute scope for activity was calculated as the difference between active and standard metabolism () and decreased from 26·18 to 14·35 μmol O₂ g^?1 h^?1 as M_WB increased. Small fish with low R_s had bigger aerobic scopes but, as expected, R_s was higher in smaller fish than larger fish. The measurements and results from this study are unique as R_s, R_a and absolute aerobic scopes have not been previously determined for small age 0 year G. morhua.     

Relationships between metabolic rate, muscle electromyograms and swim performance of adult chinook salmon

Oxygen consumption rates of adult spring chinook salmon Oncorhynchus tshawytscha increased with swim speed and, depending on temperature and fish mass, ranged from 609 mg O₂ h^?1 at 30 cm s^?1 (c. 0·5 BL s^?1) to 3347 mg O₂ h^?1 at 170 cm s^?1 (c. 2·3 BL s^?1). Corrected for fish mass, these values ranged from 122 to 670 mg O₂ kg^?1 h^?1, and were similar to other Oncorhynchus species. At all temperatures (8, 12·5 and 17° C), maximum oxygen consumption values levelled off and slightly declined with increasing swim speed >170 cm s^?1, and a third‐order polynomial regression model fitted the data best. The upper critical swim speed (U_crit) of fish tested at two laboratories averaged 155 cm s^?1 (2·1 BL s^?1), but U_crit of fish tested at the Pacific Northwest National Laboratory were significantly higher (mean 165 cm s^?1) than those from fish tested at the Columbia River Research Laboratory (mean 140 cm s^?1). Swim trials using fish that had electromyogram (EMG) transmitters implanted in them suggested that at a swim speed of c. 135 cm s^?1, red muscle EMG pulse rates slowed and white muscle EMG pulse rates increased. Although there was significant variation between individual fish, this swim speed was c. 80% of the U_crit for the fish used in the EMG trials (mean U_crit 168·2 cm s^?1). Bioenergetic modelling of the upstream migration of adult chinook salmon should consider incorporating an anaerobic fraction of the energy budget when swim speeds are ≥80% of the U_crit.     

Induced swimming modified the antioxidant status of gilthead seabream (Sparus aurata)

Swimming has relevant physiological changes in farmed fish, although the potential link between swimming and oxidative stress remains poorly studied. We investigated the effects of different medium-term moderate swimming conditions for 6 h on the antioxidant status of gilthead seabream (Sparus aurata), analyzing the activity of enzymes related to oxidative stress in the liver and skeletal red and white muscle. Forty fish were induced to swim individually with the following conditions: steady low (SL, 0.8 body length (BL)·s⁻¹), steady high (SH, 2.3 BL·s⁻¹), oscillating low (OL, 0.2–0.8 BL·s⁻¹) and oscillating high (OH, 0.8–2.3 BL·s⁻¹) velocities, and a non-exercised group with minimal water flow (MF, < 0.1 BL·s⁻¹). All swimming conditions resulted in lower activities of superoxide dismutase (SOD), glutathione reductase (GR), and glutathione-S-transferase (GST) in the liver compared to the MF group, while steady swimming (SL and SH) led to higher reduced glutathione/oxidized glutathione ratio (GSH/GSSG) compared to the MF condition. Swimming also differently modulated the antioxidant enzyme activities in red and white muscles. The OH condition increased lipid peroxidation (LPO), catalase (CAT) and glutathione peroxidase (GPx) activities in the red muscle, decreasing the GSH/GSSG ratio, whereas the SL condition led to increased GSH. Oscillating swimming conditions (OL and OH) led to lower CAT activity in the white muscle, although GPx activity was increased. The GSH/GSSG ratio in white muscle was increased in all swimming conditions. Liver and skeletal muscle antioxidant status was modulated by exercise, highlighting the importance of adequate swimming conditions to minimize oxidative stress in gilthead seabream.     

Spatial ecology of coastal Atlantic cod Gadus morhua associated with parasite load

Acoustic tags and receivers were used to investigate the spatial ecology of coastal Atlantic cod Gadus morhua (n = 32, mean fork length: 50 cm, range: 33–80 cm) on the Norwegian Skagerrak coast in 2012. Monthly home ranges (HR), swimming activity and depth use varied considerably among individuals and through the months of June, July and August. HR sizes for the period ranged from 0·25 to 5·20 km² (mean = 2·30 km²). Two thirds of the tagged G. morhua were infected with black spot disease Cryptocotyle lingua parasites; these fish had larger HRs and occupied deeper water compared with non‐infected fish. The infected fish also tended to be more active in terms of horizontal swimming. From an ecological and evolutionary perspective, any environmental change that modifies G. morhua behaviour may therefore also alter the parasite load of the population, and its conservation and fishery status.