Introduced bullheads Cottus gobio and infection with plerocercoids of Schistocephalus cotti in the Utsjoki, an Arctic river in Finland

Bullheads Cottus gobio, first found in the River Utsjoki, an Arctic river in Finland, in 1979, were sampled at six sites in August 1991 (two of these sites were also sampled previously in June and July 1991). Mean total length (L_T) of C. gobio was 45 mm (n= 1080 fish). Overall, there were slightly more females than males, with males larger than females (mean L_T males 52·1 and females 47·6 mm). Prevalence of infection with plerocercoids of Schistocephalus cotti varied from 20·0 to 43·0% over the six sites in August. Juvenile C. gobio had a prevalence of infection of 3·5% whereas in mature fish prevalence was consistently higher in females than in males (38·8 v. 20·1%). There was one plerocercoid per infected juvenile C. gobio. In mature fish the mean number varied between 1·3 and 1·8: 49% had one worm per fish, 38% two or three worms and 13% had four to eight plerocercoids. In juvenile C. gobio, S. cotti were randomly distributed (overdispersion index 1·10), whereas occurrence was slightly aggregated in the L_T groups 40–59 and ≥60 mm (overdispersion indices both 1·90). Mean mass of infected fish was higher in all L_T groups compared to uninfected C. gobio. After removal of plerocercoids, mean mass of fish tissue remaining was lower compared with uninfected fish for the two L_T groups 40–59 and ≥ 60 mm, but higher in C. gobio <40 mm L_T. Prevalence and mean intensity of infection over the 3 months did not differ either for the two sites individually or the pooled data. Mean mass of both uninfected and infected fish increased over this period, and were both highest in August as was the mean worm burden. There was, however, no difference in Fulton’s condition factor at any time. Mean mass of plerocercoids in C. gobio of ≥40 mm L_T increased significantly comparing June and July with August. Comparison of backcalculated L_T of infected and non‐infected bullheads of different age‐groups did not show any significant differences in growth at any age. In each parasite infrapopulation as the number of worms increased so their mean mass decreased significantly but at the same time the total mass of worms in the fish host remained more or less constant in relation to length. Aggregation of parasites in the fish population was low, as the majority were infected by one S. cotti plerocercoid. Gonad development was suppressed in infected C. gobio.     

Age, growth, and sexual maturity of the yellownose skate Dipturus chilensis in the south‐eastern Pacific

The age and growth parameters of Dipturus chilensis were estimated by counting growth rings from thin sections of vertebral centra from 400 fish (246 females and 154 males), ranging from 23 to 124 cm total length (L_T), and backcalculating fish lengths at previous ages. Marginal increment analysis lent support to the hypothesis of annual deposition of band‐pairs, which formed during the winter months. The oldest female D. chilensis aged in this study was 21 years and 117 cm L_T, whereas the oldest male was 18 years and 93 cm L_T. A 4·7% index of average per cent error (I_APE) suggested that this is a precise method for calculating the age of D. chilensis. Observed L_T were lower than backcalculated L_T, which implies the influence of Lee's phenomenon. The von Bertalanffy growth equations, based on mean length‐at‐age data, were estimated as L_t = 128·3 (1 ? e^{?0·112 (t + 0·514)}) for females and L_t = 107·8 (1 ? e^{?0·134 (t + 0·862)}) for males where t is age (years). Growth was significantly different between sexes: females reached a larger adult size. Ages and lengths at 50% maturity were estimated at 14 years of age and 106 cm L_T for females and 11 years of age and 86 cm L_T for males. At c. 14 years, there was a decline in growth rates in females. The factor most likely responsible for this was sexual maturity, which caused a discontinuity in growth of female fish. These results show that this species is slow‐growing, long‐lived, relatively large and of delayed maturity, characteristics that make it vulnerable to exploitation.     

Short‐term survival and movements of Atlantic sharpnose sharks captured by hook‐and‐line in the north‐east Gulf of Mexico

Ultrasonic telemetry was used to compare post‐release survival and movements of Atlantic sharpnose sharks Rhizoprionodon terraenovae in a coastal area of the north‐east Gulf of Mexico. Ten fish were caught with standardized hook‐and‐line gear during June to October 1999. Atlantic sharpnose sharks were continuously tracked after release for periods of 0·75 to 5·90 h and their positions recorded at a median interval of 9 min. Individual rate of movement was the mean of all distance and time measurements for each fish. Mean ± s.e . individual rate of movement was 0·45 ± 0·06 total lengths per second (L_T s^?1) and ranged from 0·28 to 0·92 L_T s^?1 over all fish. Movement patterns did not differ between jaw and internally hooked Atlantic sharpnose sharks. Individual rate of movement was inversely correlated with bottom water temperature at capture (r² = 0·52, P ≤ 0·05). No consistent direction in movement was detected for Atlantic sharpnose sharks after release, except that they avoided movement towards shallower areas. Capture‐release survival was high (90%), with only one fish not surviving, i.e. this particular fish stopped movement for a period of 10 min. Total rate of movement was total distance over total time (m min^?1) for each Atlantic sharpnose shark. Mean total rate of movement was significantly higher immediately after release at 21·5 m min^?1 over the first 1·5 h of tracking, then decreased to 11·2 m min^?1 over 1·5–6 h, and 7·7 m min^?1 over 3–6 h (P ≤ 0·002), which suggested initial post‐release stress but quick recovery from capture. Thus, high survival (90%) and quick recovery indicate that the practice of catch‐and‐release would be a viable method to reduce capture mortality for R. terraenovae.     

Extraordinary growth in tiger sharks Galeocerdo cuvier from the South Atlantic Ocean

Two tagged‐and‐recaptured tiger sharks Galeocerdo cuvier, measuring 172 and 304 cm total length (L_T) and at age 0·75 and 3·50 years, exhibited unmatched growth rates of 118·4 and 55·5 cm year^?1, respectively. The larger fish was nearly mature, indicating that G. cuvier off Brazil could mature considerably earlier than conspecifics from other regions.     

Life‐history traits of the long‐nosed skate Dipturus oxyrinchus

This work investigates life‐history traits of the long‐nosed skate Dipturus oxyrinchus, which is a common by‐catch in Sardinian waters. The reproductive variables were analysed from 979 specimens sampled during scientific and commercial hauls. Females (10·4–117·5 cm total length, L_T) attained larger sizes than males (14·5–99·5 cm L_T). To evaluate age and growth, a sub‐sample of 130 individuals (76 females and 54 males) were used. The age was estimated by annuli counts of sectioned vertebral centra. Four models were used for the length‐at‐age data: the von Bertalanffy, the exponential, the Gompertz and the logistic functions. According to the Akaike's information criterion, the Gompertz model seemed to provide the best fitting curve (L_∞ mean ± s.e. : 127·55 ± 4·90 cm, k: 0·14 ± 0·09, IP: 3·97 ± 0·90 years). The oldest female and male were aged 17 (115·5 cm L_T) and 15 years (96·0 cm L_T), respectively. Lengths at maturity were 103·5 cm for females and 91·0 cm for males, corresponding to 90% of the maximum observed length in both sexes. The monthly distribution of maturity stages highlighted an extended reproductive cycle, with spawning females and active males being present almost throughout the year, as confirmed by the gonado‐somatic index. Ovarian fecundity reached a maximum of 26 yolked follicles with a mean ± s.e. size of 19·7 ± 6·5 mm.     

Reproductive biology and feeding habits of the prickly dogfish Oxynotus bruniensis

The reproductive biology and diet of prickly dogfish Oxynotus bruniensis, a deep‐sea elasmobranch, endemic to the outer continental and insular shelves of southern Australia and New Zealand, and caught as by‐catch in demersal fisheries, are described from specimens caught in New Zealand waters. A total of 53 specimens were obtained from research surveys and commercial fisheries, including juveniles and adults ranging in size from 33·5 to 75·6 cm total length (L_T). Estimated size‐at‐maturity was 54·7 cm L_T in males and 64·0 cm L_T in females. Three gravid females (65·0, 67·5 and 71·2 cm L_T) were observed, all with eight embryos. Size‐at‐birth was estimated to be 25–27 cm L_T. Vitellogenesis was not concurrent with embryo development. Analysis of diet from stomach contents, including DNA identification of prey using the mitochondrial genes cox1 and nadh2, revealed that O. bruniensis preys exclusively on the egg capsules of holocephalans, potentially making it the only known elasmobranch with a diet reliant solely upon other chondrichthyans. Based on spatial overlap with deep‐sea fisheries, a highly specialized diet, and reproductive characteristics representative of a low productivity fish, the commercial fisheries by‐catch of O. bruniensis may put this species at relatively high risk of overfishing.     

Population biology of an endangered species: the common guitarfish Rhinobatos rhinobatos in Lebanese marine waters of the eastern Mediterranean Sea

This study focuses on the population biology of the common guitarfish Rhinobatos rhinobatos, a cartilaginous fish listed as Endangered in the International Union for the Conservation of Nature (IUCN) Red List. Between December 2012 and January 2014, 67 individuals were collected by bottom longlining in coastal Lebanese marine waters at different ports at depths ranging from 10 to 110 m. The total length (L_T) of the specimens ranged from 50 to 143 cm, and the mean ± s.d . was 76·2 ± 19·7 cm. The most common L_T classes were between 60 and 70 cm. The total mass of the specimens ranged from 410 to 10 000 g, and the mean ± s.d . was 1841 ± 1987 g. A total of 34 males and 33 females were collected, and the sex ratio was not significantly different from 1:1. The mass and L_T relationship showed positive allometric growth (b = 3·096 and r² = 0·99), and the mean ± s.d . L_T at which 50% of the individuals were sexually mature was 84·73 ± 5·81 cm for females and 78·57 ± 4·88 cm for males. The gonado‐somatic and hepato‐somatic indices were determined along with a condition factor, and parturition appeared to occur in winter. The primary prey items found in the fish stomachs during the autumn and winter seasons were Penaeidae. The results of this study will help to parameterize models of the population dynamics for this exploited fish stock to ensure the long‐term sustainability of its fishery.     

Investigating trophic‐level variability in Celtic Sea fish predators

The trophic level (T_L) mean and variance, and the degree of omnivory for five Celtic Sea fish predators were estimated using a database of stomach content records characterized by a high level of taxonomic resolution. The predators occupied a high position in the food web, i.e. 4·75 for Atlantic cod Gadus morhua, 4·44 for haddock Melanogrammus aeglefinus, 4·88 for European hake Merluccius merluccius, 5·00 for megrim Lepidorhombus whiffiagonis and 5·27 for whiting Merlangius merlangus. The level of taxonomic resolution of the prey did not greatly affect mean T_L predator values; an effect on variance was evident, low resolution masking intra‐population variability in T_L. Generalized additive models (GAM) were used to explain the variability of predator T_L caused by environmental variables (International Council for the Exploration of the Sea, ICES, division and season) and predator characteristics (total length, L_T). Significant year, location season and interaction effects were found for some species and with L_T at the scale of ICES subdivision. The species‐specific variability of T_L could be due to spatio‐temporal variations in prey availability and in predator selectivity following ontogenetic changes. Omnivorous fish T_L was less affected by spatio‐temporal variations. In addition, results showed that the omnivory index and T_L variability provide dissimilar information on predator feeding strategy. Combining information on T_L variability and omnivory allowed between within‐individual and between‐individual components contributing to trophic niche width to be separated and the type of generalization of fish predators to be identified.     

Skeletal ontogeny of the vertebral column and of the fins in shi drum Umbrina cirrosa (Teleostei: Perciformes: Sciaenidae), a new candidate species for aquaculture

The osteological development of the vertebral column and fins in shi drum Umbrina cirrosa was studied in order to improve knowledge for its introduction in Mediterranean aquaculture. The osteological development was studied in 171 individuals, of total length (L_T) from 2·7 to 30·2 mm that were reared under the mesocosm technique. Vertebral ontogeny starts at 3·4 and 4·0 mm L_T, with the formation of the first cartilaginous neural and haemal arches, and spines, respectively, and is completed with the full attainment of epicentrals (12·5 mm L_T). The formation of vertebral centra occurs between 4·1 and 7·4 mm L_T. Pectoral supports are the first fin elements to develop (3·0 mm L_T), followed by those of the caudal fin (3·8 mm L_T), pelvic fin (3·9 mm L_T) and finally by those of the dorsal and anal fins (4·5 mm L_T). The caudal fin is the first to develop fin rays and attain the full count of principal fin rays (4·5–6·8 mm L_T), but the last to be fully completed with the formation of procurrent fin rays (6·9–17·5 mm L_T). The next fins starting to present rays are the dorsal (5·3 mm L_T) and the pectoral fins (5·6 mm L_T), while the anal and pelvic fins are the last (5·7 mm L_T). Following the caudal principal fin rays (6·8 mm L_T), the dorsal, anal (6·9 mm L_T), pelvic (7·4 mm L_T) and pectoral fins (9·8 mm L_T) are the next with fully completed ray counts. Aggregation of qualitative changes, such as the appearance of cartilages, the beginning and the complement of the ossification process and the full complement of elements in U. cirrosa were measured as cumulative frequency counts. These measurements reveal three ontogenetic intervals: one very developmentally active period during early life stages (from 3 to 5·9 mm L_T), a second slower developmental period (from 6·0 to 8·9 mm L_T) and finally a period of ontogeny more focused on structure refinement up to metamorphosis and settlement (>9·0 mm L_T).     

Static habitat partitioning and dynamic selection by sympatric young Atlantic salmon and brown trout in south-west England streams

Direct underwater observation of micro‐habitat use by 1838 young Atlantic salmon Salmo salar [mean L_T 7·9 ± 3.1(s.d.) cm, range 3·19] and 1227 brown trout Salmo trutta (L_T 10·9 ± 5·0 cm, range 3·56) showed both species were selective in habitat use, with differences between species and fish size. Atlantic salmon and brown trout selected relatively narrow ranges for the two micro‐habitat variables snout water velocity and height above bottom, but with differences between size‐classes. The smaller fishes <7 cm held positions in slower water closer to the bottom. On a larger scale, the Atlantic salmon more often used shallower stream areas, compared with brown trout. The larger parr preferred the deeper stream areas. Atlantic salmon used higher and slightly more variable mean water velocities than brown trout. Substrata used by the two species were similar. Finer substrata, although variable, were selected at the snout position, and differences were pronounced between size‐classes. On a meso‐habitat scale, brown trout were more frequently observed in slow pool‐glide habitats, while young Atlantic salmon favoured the faster high‐gradient meso‐habitats. Small juveniles <7 cm of both species were observed most frequently in riffle‐chute habitats. Atlantic salmon and brown trout segregated with respect to use of habitat, but considerable niche overlap between species indicated competitive interactions. In particular, for small fishes <7 cm of the two species, there was almost complete niche overlap for use of water depth, while they segregated with respect to water velocity. Habitat suitability indices developed for both species for mean water velocity and water depth, tended to have their optimum at lower values compared with previous studies in larger streams, with Atlantic salmon parr in the small streams occupying the same habitat as favoured by brown trout in larger streams. The data indicate both species may be flexible in their habitat selection depending on habitat availability. Species‐specific habitat overlap between streams may be complete. However, between‐species habitat partitioning remains similar.     

Diel vertical migrations of bathypelagic perch fry

The behaviour of young‐of‐the‐year (YOY) perch Perca fluviatilis as a dominant species in the assemblage of fry in the pelagic of Slapy Reservoir (Czech Republic), was studied during late May and mid‐June 2002 using acoustic methods and complementary net catches. During the day, perch fry were present simultaneously in littoral, epipelagic and bathypelagic habitats. Bathypelagic perch fry, forming a scattering layer, migrated vertically each day between the epilimnion and hypolimnion, with an amplitude of 11·0 m in May and 12·5 m in June. At dusk, the migratory bathypelagic fry mixed in the epilimnion with non‐migrating epipelagic fry and spent the night close to the thermocline (abundance maximum at 3–4 m in May, 0–2 m in June). In June, shoaling behaviour by some of the bathypelagic perch fry was also observed: the shoaling fry remained higher in the water column than the non‐shoaling fry. Both depths of the scattering layer and the depths of the fry shoals were strongly controlled by the light intensity. The contribution of the bathypelagic part of the population to the total numbers of pelagic perch fry decreased from 28·1% in May to 4·7% in June, while the density of all pelagic perch fry increased (c. 96 000 individuals ha^?1 in May and 142 000 individuals ha^?1 in June). In May, the bathypelagic (average total length, L_T, 11·9 mm) and epipelagic (average L_T 14·6 mm) perch fry differed in size while, in June, the epipelagic fry were divided into two distinct size groups. The more abundant group, of small epipelagic perch fry (average L_T 14·6 mm), was similar in size to the bathypelagic fry (average L_T 14·6 mm) while the less abundant group, of larger epipelagic fry (average L_T 34·4 mm), was similar in size to littoral perch fry (average L_T 35·0 mm). The results suggest that in perch fry three different survival strategies with different risks can be used in the same locality, time and year.     

Biochemical composition of a dominant detritivorous fish Prochilodus lineatus along pollution gradients in the Paraná-Río de la Plata Basin

The biochemical composition of muscle, liver and stomach contents of a detritivorous fish Prochilodus lineatus was analysed and compared to settling particles and sediments along pollution gradients over 1500 km of the Río de la Plata Basin to evaluate the effects of anthropogenic discharges in a detritus food chain. The stomach contents of P. lineatus collected in the polluted Metropolitan Buenos Aires coast were enriched in proteins, carbohydrates and lipids, similar to settling particulates collected in the sewer area, and two to five times higher than underlying sediments, supporting the interpretation that P. lineatus feeds on unconsolidated organic flocs freshly decanted from mixed industrial and sewage outfalls. Fish from Buenos Aires had consistently higher standard length (L_S) and mass (M_T) slopes (b = 3·5), condition indexes (K = 3·01 ± 0·47, mean ±s.d .) and muscle fat content (fat = 23·8 ± 13·8% wet mass, mean ±s.d .) relative to northern fish (b = 2·7, K = 2·22 ± 0·39, fat = 3·4 ± 3·2% wet mass, respectively), suggesting that sewage‐derived organic matter was an enriched diet, which allowed an enhanced body mass gain and fat accumulation compared to organic‐poor vegetal detritus in the north Paraná area. Buenos Aires fish also showed higher hepato‐somatic indices (mean ±s.d . I_H 1·41 ± 0·49 v. 0·70 ± 0·32, respectively), which correlated with their two to three orders of magnitude higher hydrocarbon and polychlorinated biphenyl (PCB) loads, suggesting an enhanced detoxifying metabolism. The northward migration of fatty P. lineatus was evidenced by the presence of clear outliers in the L_S and M_T relationship, K and fat content along the Paraná River.     

Reproductive aspects of the Atlantic angel shark Squatina dumeril in the southern Caribbean Sea

The maturity and reproduction of the Atlantic angel shark Squatina dumeril were assessed using 77 females (29·2–110·4 cm total length; L_T) and 269 males (58·7–108·2 cm L_T) harvested by artisanal gillnetters off Venezuela. The biased sex ratio implied segregation or sex‐specific gear selectivity. Based on the development of the reproductive tract, 50% L_T at sexual maturity (L_T50, mean ± s.e .) for females and males were estimated at 86·14 ± 0·64 and 81·55 ± 0·12 cm, respectively. Uterine fecundity ranged between one and six and with a maximum embryo size of 25·7 cm L_T. Gravid females were observed from August to December, including those close to parturition and while the gestation period was not confirmed, the size of ovarian follicles among some specimens implied protraction. The low fecundity of the species supports close monitoring of catches.     

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.     

Riverine and near coastal migration performance of hatchery brown trout Salmo trutta

To study migration performance and return rates of hatchery brown trout Salmo trutta smolts the first 5 months after release, 50 fish in each year (fork length, L_F, 158–288 mm) were in two subsequent years tagged with acoustic transmitters and recorded by automatic listening stations in the River Nidelva (central Norway), its estuary and in the marine environment. More than half of the smolts became anadromous migrants (52% in 2011 and 70% in 2012). The fish spent longer time in the estuary than in the marine environment and the results suggest that migratory behaviour of S. trutta smolts is not only restricted to be resident or anadrome–lacustrine, but that there is also an intermediary strategy of estuarine feeding. There were no differences in L_F or mass between groups of smolts with different migration patterns. Return rates from the sea within the first 5 months after release were in both years 16%. Median progression rate in the river was 0·090 L_F s^?1 but decreased significantly as the smolts entered the estuary (0·015 L_F s^?1). The long residential time in the estuary may increase the risk of negative effects of anthropogenic activities in estuaries, such as harbours and industrial development, and special attention should be given to evaluate effects of such activities.     

Larval and juvenile development of dusky grouper Epinephelus marginatus reared in mesocosms

The larval development of the dusky grouper Epinephelus marginatus up to the benthic juvenile stage is described in detail to establish a reference for their larval identification. Development is described in terms of ontogenetic changes in morphology, growth, pigmentation, fin structure and skeletal structure. Larvae were reared in mesocosms at a mean temperature of 24·3° C, salinity of 36·5, dissolved oxygen of 6·4 mg l^?1 and pH of 8·2. Newly hatched larvae had an estimated total length (L_T) of 2·3 mm. On the second day post hatching the yolk was almost fully absorbed with traces of the oil globule still present, the eyes were already pigmented and mouth and gut functional. At this stage the cranial skeletal elements for feeding and breathing (mouth and gills) and the pectoral‐fin support were already present. About 50% of the observed larvae had food in their guts. Pigmentation was very characteristic, consisting of two large chromatophores visible on the edge of the primordial fin, close to the midpoint of the post‐anal region of the body and over the midgut and hindgut and post‐anal portion of the body. At 2·9 mm L_T the emergence of the second dorsal‐fin spine, characteristic of the Epinephilinae, was clearly visible. The pre‐flexion stage started in larva of 3·2 mm L_T. At 5·5 mm L_T the larvae possessed posterior preopercular angle spines, and the dorsal and pelvic spines presented serrated edges and were pigmented. The water surface‐tension‐related death of the yolk sac and pre‐flexion larvae described in the rearing of several other grouper species did not occur during E. marginatus culture. Notochord flexion, with initial ossification of the caudal‐fin supporting elements, started at 6·6 mm L_T. At this stage the major melanophores, preopercular, dorsal and pelvic spines and mandibular teeth were already present. Transformation of larvae into juveniles occurred when larvae averaged 13·8 mm L_T. Juveniles with a mean L_T of 20·1 mm started to settle and most of them were benthic with a mean L_T of 26·8 mm.     

Thermal tolerance and metabolic physiology among redband trout populations in south‐eastern Oregon

Streamside measurements of critical thermal maxima (T_crit), swimming performance (U_crit), and routine (R_r) and maximum (R_max) metabolic rates were performed on three populations of genetically distinct redband trout Oncorhynchus mykiss in the high‐desert region of south‐eastern Oregon. The T_crit values (29·4 ± 0·1° C) for small (40–140 g) redband trout from the three streams, and large (400–1400 g) redband trout at Bridge Creek were not different, and were comparable to published values for other salmonids. At high water temperatures (24–28° C), large fish incurred higher metabolic costs and were more thermally sensitive than small fish. U_crit(3·6 ± 0·1 L_F s^?1), R_r(200 ± 13 mg O₂ kg^?0·830 h^?1) and metabolic power (533 ± 22 mg O₂ kg^?0·882 h^?1) were not significantly different between populations of small redband trout at 24° C. R_max and metabolic power, however, were higher than previous measurements for rainbow trout at these temperatures. Fish from Bridge Creek had a 30% lower minimum total cost of transport (C_min), exhibited a lower refusal rate, and had smaller hearts than fish at 12‐mile or Rock Creeks. In contrast, no differences in U_crit or metabolism were observed between the two size classes of redband trout, although C_min was significantly lower for large fish at all swimming speeds. Biochemical analyses revealed that fish from 12‐mile Creek, which had the highest refusal rate (36%), were moderately hyperkalemic and had substantially lower circulating levels of free fatty acids, triglycerides and albumin. Aerobic and anaerobic enzyme activities in axial white muscle, however, were not different between populations, and morphological features were similar. Results of this study: 1) suggest that the physiological mechanisms that determine T_crit in salmonids are highly conserved; 2) show that adult (large) redband trout are more susceptible to the negative affects of elevated temperatures than small redband trout; 3) demonstrate that swimming efficiency can vary considerably between redband trout populations; 4) suggest that metabolic energy stores correlate positively with swimming behaviour of redband trout at high water temperatures; 5) question the use of T_crit for assessing physiological function and defining thermal habitat requirements of stream‐dwelling salmonids like the redband trout.     

Interaction between migration behaviour and estuarine mortality in cultivated Atlantic salmon Salmo salar smolts

Migration behaviour and estuarine mortality of cultivated Atlantic salmon Salmo salar smolts in a 16 km long estuary were studied using two methods: (1) acoustic telemetry and (2) group tagging in combination with trap nets. Progression rates of surviving individuals through the estuary were relatively slow using both methods [0·38 L_T (total length) s^?1 v. 0·25 L_T s^?1]. In 2012, the progression rate was slow from the river to the estuary (0·55 L_T s^?1) and the first part of the estuary (0·31 L_T s^?1), but increased thereafter (1·45–2·21 L_T s^?1). In 2013, the progression rate was fast from the river to the estuary (4·31 L_T s^?1) but was slower thereafter (0·18–0·91 L_T s^?1). Survival to the fjord was higher in 2012 (47%) compared to 2013 (6%). Fast moving individuals were more likely to migrate successfully through the estuary compared to slower moving individuals. Adult recapture of coded‐wire‐tagged S. salar was generally low (0·00–0·04%). Mortality hot spots were related to topographically distinct areas such as the river outlet (in 2012) or the sill separating the estuary and the fjord (in 2013). At the sill, an aggregation of cod Gadus morhua predating on cultivated smolts was identified. The results indicate that slow progression rates through the estuary decreases the likelihood of smolts being detected outside the estuary. The highly stochastic and site‐specific mortality patterns observed in this study highlight the complexity in extrapolating mortality patterns of single release groups to the entire smolt run of wild S. salar.