Migrations of sea trout, Salmo trutta L., from the Vardnes river in northern Norway

During the periods 1956–1963 and 1967–1970 traps were operated to catch upstream- and downstream-migrating sea trout, Salmo trutta L. A total of 15 788 sea trout were tagged, using Carlin tags. The number of recaptures made in the traps was 4481, of which 1796 were recaptured more than once.
The distribution of the 2122 recaptures in the sea provides a picture of the sea-migration pattern. Of the sea recaptures, 52.8% were reported as within a distance of 3 km from the river mouth, compared to 0.7% more than 80 km away. All the different size-groups of sea trout were represented among both the long-distance and the short-distance migrants. The results of this study of sea trout migrations are discussed in relation to the published results for Atlantic salmon, Salmo salar L., and sea charr, Salvelinus alpinus (L.), from the same river.
The four highest values recorded for mean distance of daily travel away from the river were 20, 8, 8 and 6km day⁻¹ by smolts and 6, 6, 5 and 5km day⁻¹ by larger-sized sea trout.
Recaptures of tagged sea trout in rivers other than the Vardnes totalled 506, of which 306 had been tagged as smolts. The calculated minimum percentage of stray is 15.5%. The proportion of sea trout from the Vardnes river that actually spawn in other rivers is not known. No significant difference in length distribution was found between the sea trout caught in the Vardnes river and those caught in other rivers. An hypothesis concerning the selective advantages of straying by anadromous salmonids living in small rivers is discussed.     

Post- stocking movements and recapture of hatchery-reared trout released into flowing waters—effect of prior acclimation to flow

Hatchery-reared brown trout, Salmo trutta , (f.l., 16–27 cm) were stocked into the Afon Clettwr, Afon Western Cleddau and Afon Dysynni, Wales. The effects of (a) retaining fish caged in the river for 24 h before release, and (b) a period of acclimation to flowing water (up to 0.24 m s⁻¹) in tanks prior to stocking were investigated. Data on percentage recapture and post-stocking movements were obtained from trapping, electrofishing and tag returns. In-stream acclimation resulted in a higher percentage recapture and a more limited dispersion of the fish stocked under low river flow conditions, but had no effect on trout stocked into a river where higher water velocities were experienced. Acclimation, in tanks, to a flow of 0.1 ms⁻¹ for 14 days led to higher percentage recaptures, whereas acclimation for only 2 days resulted in fewer returns than for unacclimated fish. No differences in fish distribution within the rivers could be attributed to these acclimation procedures.     

Reproductive migration of brown trout in a small Norwegian river studied by telemetry

The movement of 34 large (39–73 cm standard length) brown trout Salmo trutta was monitored using radio telemetry for up to 74 days in Brumunda, a small Norwegian river (mean annual discharge 3·3 m³ s⁻¹) flowing into the large Lake Mjøsa. The maximum range of movement in the river was 20 km. No clear relationships existed between individual movement and water discharge, temperature and barometric pressure. Brown trout migrated at all levels of water discharge. At low discharge (<2 m³ s⁻¹) movements were nocturnal. A weir 5·3 km from the outlet restricted ascending brown trout at low ( c . 6° C), but not at high ( c . 8° C) water temperatures. Spawning occurred in September to October and tagged individuals spent 2–51 days at the spawning sites. Mean migration speed from tagging to when the fish reached the spawning area, and from when they left the spawning areas and reached the lake was 1·0 and 2·3 km day⁻¹, respectively. All tagged brown trout that survived spawning returned to the lake after spawning.     

Modelling competition and hybridization between native cutthroat trout and nonnative rainbow and hybrid trout

Native salmonid fish have been displaced worldwide by nonnatives through hybridization, competition, and predation, but the dynamics of these factors are poorly understood. We apply stochastic Lotka-Volterra models to the displacement of cutthroat trout by rainbow/hybrid trout in the Snake River, Idaho, USA. Cutthroat trout are susceptible to hybridization in the river but are reproductively isolated in tributaries via removal of migratory rainbow/hybrid spawners at weirs. Based on information-theoretic analysis, population data provide evidence that hybridization was the primary mechanism for cutthroat trout displacement in the first 17 years of the invasion. However, under some parameter values, the data provide evidence for a model in which interaction occurs among fish from both river and tributary subpopulations. This situation is likely to occur when tributary-spawned cutthroat trout out-migrate to the river as fry. The resulting competition with rainbow/hybrid trout can result in the extinction of cutthroat trout even when reproductive segregation is maintained.     

Homing behaviour of stream-dwelling brook charr following experimental displacement

Precise homing of 24 brook charr Salvelinus fontinalis (157–215 mm L_F), displaced from their site of capture in a natural stream, was rare both in fish displaced upstream and those displaced downstream. Most fish settled in preferred habitats (pool or glide) away from their home site and showed restricted movement up to the pre-spawning period. Partial return responses, however, were stronger in fish displaced downstream than in fish displaced upstream. Most fish displaced downstream showed directional upstream movement soon after displacement, whereas fish displaced upstream did not show directional upstream movement, suggesting that it is primarily olfactory cues from upstream locations, and not positive rheotaxis, which mediate the return response. Homing success was unrelated to distance of displacement, body size, or population density in the home site, but daily mobility increased with body size for fish displaced downstream. There was no evidence of switching between specific areas between night and day, nor of differences between daytime and night-time mobility, suggesting that diel movement cycles did not bias the evaluation of homing success. Site attachment in stream-dwelling brook charr may be characterized as persistent (undisturbed fish remain stationary over long periods), but readily disrupted by involuntary displacement.     

Modelling competition and hybridization between native cutthroat trout and nonnative rainbow and hybrid trout

Native salmonid fish have been displaced worldwide by nonnatives through hybridization, competition, and predation, but the dynamics of these factors are poorly understood. We apply stochastic Lotka–Volterra models to the displacement of cutthroat trout by rainbow/hybrid trout in the Snake River, Idaho, USA. Cutthroat trout are susceptible to hybridization in the river but are reproductively isolated in tributaries via removal of migratory rainbow/hybrid spawners at weirs. Based on information-theoretic analysis, population data provide evidence that hybridization was the primary mechanism for cutthroat trout displacement in the first 17 years of the invasion. However, under some parameter values, the data provide evidence for a model in which interaction occurs among fish from both river and tributary subpopulations. This situation is likely to occur when tributary-spawned cutthroat trout out-migrate to the river as fry. The resulting competition with rainbow/hybrid trout can result in the extinction of cutthroat trout even when reproductive segregation is maintained.     

Competitive habitat displacement of brown trout by Siberian sculpin: the role of size and density

Habitat competition in brown trout Salmo trutta and Siberian sculpin Cottus poecilopus was investigated by varying density, fish size, and species composition in stream channels providing areas of different substratum particle sizes. In allopatry, both small (52 ± 4 mm L _T) and large (86 ± 6 mm L _T) brown trout exhibited strong preference for the intermediate (8–11 cm diameter) and large (17–21 cm) gravel substrata. There was a tendency for more brown trout to occupy finer (2–4 cm) substrata with increasing density, in particular for large brown trout. Also, more small brown trout were observed on finer substrata when tested with large brown trout, suggesting interspecific competition for restricted space. Both small (56 ± 6 mm L _T) and large (88 ± 10 mm L _T) Siberian sculpin preferred the large gravel in all tests, and did not change their substratum preferences much with increasing densities, suggesting higher tolerance for 'crowding'. The large Siberian sculpin preferred the coarser substratum, and the largest individuals were consistently found on it. In sympatry with large Siberian sculpin, habitat displacement of brown trout occurred, indicative of interspecific competition. A higher proportion of small and large brown trout occupied the finer substrata than in allopatry. Habitat selection by large Siberian sculpin appeared to be unaffected by species composition and density. Small Siberian sculpin were displaced to finer substrata when tested with large Siberian sculpin, suggesting intraspecific competition. The results indicate that Siberian sculpin are potential habitat competitors for young brown trout.     

Optimum energy intake and gross efficiency of energy conversion for brown trout, Salmo trutta, feeding on invertebrates or fish

1. The chief objectives were to determine the daily optimum energy intake ( C OPT cal day−1) for growth and the gross efficiency ( K G%) for converting energy intake into growth for brown trout, Salmo trutta . Energy budgets for individual fish were obtained from experiments with 292 trout (initial live weight 1–318 g) bred from wild parents, and kept at five constant temperatures (5, 10, 13, 15, 18 °C) and 100% oxygen saturation. Most trout (252) were fed over a period of 42 days on a fixed ration of shrimps, Gammarus pulex , the ration levels varying between zero and maximum, but 40 of the larger trout were fed to satiation on freshly-killed sticklebacks ( Gasterosteus aculeatus ).
2. Energetics models developed in earlier studies on the same data were summarized briefly and were used to predict the relationship between the change in the total energy content of a trout ( C G cal day−1) and its energy intake ( C IN cal day−1), and hence to estimate C OPT. The models were also used to predict the relationship between K G and C IN. In both comparisons, there was good agreement between observed values from the experiments and expected mean values predicted from the models. For trout feeding on invertebrates, C OPT lay closer to the maximum, rather than the maintenance, energy intake. When the diet changed from invertebrates to fish, there was a marked increase in C IN, C G and K G.
3. For trout feeding on invertebrates, K G exceeded 30% within 7–11 °C, with a maximum K G of 31.8% at 8.9 °C. For piscivorous trout, K G exceeded 30% within 4–16 °C and 40% within 6.5–12 °C, with a maximum K G of 41.8% at 9.3 °C. These differences were discussed in relation to the results of previous workers, and the models used in the present study provided a method of exploring the limitations of the ' K -line' hypothesis for the relationship between K G and C IN.     

Stocking hatchery‐reared brown trout in different densities into a wild population – a comparison of growth and movement

In spring 2001 and 2002 a small stream was stocked with tagged hatchery‐reared yearling brown trout ( Salmo trutta ), in order to study their influence on the resident brown trout population. The stream was separated into six sections: two sections without stocking, two sections where stocking doubled the trout population and two sections where the fish population was quadrupled. The working hypothesis was that due to food limitation (competition) growth of the wild fish will be negatively influenced by stocking, and wild fish will be displaced by the (possibly more aggressive) hatchery fish. Surprisingly, growth rate of wild and stocked fish of the same age was similar and independent of stocking density. Two main reasons may be responsible for this finding: only a low percentage of the stocked fish remained in the stream, and food was not limited during summer. Only 12–19% of the stocked fish were recaptured after six months, in contrats to 40–70% of one‐year old and up to 100% of older wild trout. The wild fish were not displaced by hatchery‐reared fish: During summer the wild fish remained more or less stationary, whereas most of the stocked trout had left their release site. The results indicate that in a natural stream stocking of hatchery reared brown trout does not influence negatively growth and movement of the wild fish independent of stocking density.     

Effects of sedimentation on the gravels of an industrial river system

The natural recovery of trout ( Salmo trutta L.) populations in an industrial river, the Ebbw Fawr, South Wales, has been depressed by problems of natural recruitment. Rainbow trout ( Salmo gairdneri Richardson) eggs were planted in river gravels to assess the effects of siltation on salmonid spawning success. In reaches where siltation due to the coal industry has occurred, 98–100% of eggs died during incubation in the gravels. Experiments using standpipe techniques measured gravel permeabilities and rates of dissolved oxygen (DO) supply to artificially planted eggs, the results showed a strong dependence of hatching success and alevin size on these two parameters. The median lethal DO supply rate was about 50 μg cm^-2 h^-1.     

Some physical and chemical effects of the Cow Green (Upper Teesdale) impoundment

SUMMARY. The paper describes observations on water temperature and dissolved oxygen in Cow Green reservoir and also changes caused by impoundment to temperature, chemistry, dissolved oxygen and the discharge regime of the River Tees immediately downstream of the dam.
Impoundment and river regulation have considerably smoothed-out fluctuations in discharge of the Tees and have ehminated the very low and very high discharges which were characteristic of the natural river.
Reservoir water levels show an annual pattern of draw-down during summer, refilling in autumn and overflow during winter and spring. Tliermal stratification of the reservoir occurs rarely and is generally of short duration. Water temperatures at mid-reservoir correspond closely to those of water discharged from the reservoir. The temperature regime in the river downstream is modified as follows:

• (1)

  reduction in amplitude of annual temperature fluctuations by 1–2°C,
• (2)

  marked reduction of diel fluctuations, (3) delay of the spring rise in water temperature by 20–50 days and of the autumn fall by 0–20 days. These temperature changes could reduce the annual maintenance ration of a 10 g brown trout ( Salmo trutta L.) by about 15% and delay the annual peak of metabolism by about 1 month. The effect upon growth rate of trout would be negligible.

Fluctuations in ionic content at the reservoir inflow are comparatively large and can be related approximately to river discharge. Fluctuations at the outflow are smaller and appear to be largely seasonal. Regulation has not appreciably altered the dissolved oxygen content of the River Tees.     

The feeding response of diploid and triploid Atlantic salmon and brook trout

Pair and group experiments were conducted to determine whether differences exist in feeding success between juvenile diploid and triploid salmonids in a competitive situation. In the pair experiments, 22 pairs (one diploid and one triploid) of size-matched Quebec-strain brook trout Salvelinus fontinalis (7·2–46·3 g) were fed an unlimited number of pellets three times a day for 5 days. Dominance was assigned to the fish which ate the most pellets within each pair. In the group experiments, groups of three diploid and three triploid size-matched fish were fed a restricted ration three times a day for 5 days. Hierarchical rank within the group was assigned based on the number of pellets consumed by each fish. The group experiment was repeated 10 times with Atlantic salmon Salmo salar (5·1–62·7 g), Quebec-strain brook trout (11·8-110·8 g), and large UNB-strain brook trout (18·2–33·0 g), and 12 times with smaller UNB-strain brook trout (0·6–2·0 g). A statistically significant difference in rank between ploidies was found only for the smaller UNB-strain brook trout in the group experiments, with diploids dominant over triploids. This suggests that there may be a difference in competitive feeding success between diploid and triploid brook trout early in development, but that this difference diminishes as the fish grow.     

Temporal variability in marine feeding of sympatric Arctic charr and sea trout

The marine feeding pattern of anadromous brown trout (sea trout) Salmo trutta and Arctic charr Salvelinus alpinus was studied during June to August in 1992–1993 and 2000–2004 in a fjord in northern Norway. In general sea trout fed proportionally more on fishes than on crustaceans and insects (81, 1 and 18% by mass, respectively) by comparison with Arctic charr (52, 25 and 22% by mass, respectively). Herring Clupea harengus dominated the total fish diet of both species, but the Arctic charr also fed significantly on gadoids and sandlance Ammodytes spp. While sea trout became virtually all piscivorous at fork lengths ( L _F) ≥250 mm, the Arctic charr was ≥400 mm L _F before shifting totally to a fish diet. Despite annual variation in diet and forage ratios, there was a clear shift in diet from 1992–1993 to 2000–2004. Sandlance and different crustaceans constituted most of the diet during the initial period with a shift towards gadoids and especially herring during the latter period. This shift seemed to be associated with a high abundance of herring larvae during the latter sampling period, indicating a preferential selection on herring when present, particularly by sea trout. Furthermore, an index indicated dietary overlap in years with intensive feeding on herring of both species, and usually differences in the trophic ecology during years feeding mostly on other prey species. In combination, it was hypothesized that the two species reflect the type of marine prey present within a fjord system over time, and therefore provide an index of variation in the production and biological diversity of their potential prey within fjords.     

Migration of hatchery‐reared Atlantic salmon and wild anadromous brown trout post‐smolts in a Norwegian fjord system

Hatchery‐reared Atlantic salmon Salmo salar ( n  = 25) and wild anadromous brown trout (sea trout) Salmo trutta ( n  = 15) smolts were tagged with coded acoustic transmitters and released at the mouth of the River Eira on the west coast of Norway. Data logging receivers recorded the fish during their outward migration at 9, 32, 48 and 77 km from the release site. Seventeen Atlantic salmon (68%) and eight sea trout (53%) were recorded after release. Mean migratory speeds between different receiver sites ranged from 0·49 to 1·82 body lengths (total length) per second (bl s⁻¹) for Atlantic salmon and 0·11–2·60 bl s⁻¹ for sea trout. Atlantic salmon were recorded 9, 48 and 77 km from the river mouth on average 28, 65 and 83 h after release, respectively. Sea trout were recorded 9 km from the release site 438 h after release. Only four (23%) sea trout were detected in the outer part of the fjord system, while the rest of the fish seemed to stay in the inner fjord system. The Atlantic salmon stayed for a longer time in the inner part than in the outer parts of the fjord system, but distinct from sea trout, migrated through the whole fjord system into the ocean.     

Seasonal changes in the body composition of young riverine Atlantic salmon and brown trout

The body composition of protein and fat in Atlantic salmon Salmo salar and brown trout Salmo trutta before and after winter was investigated in a temperate, small river, normally ice covered from the middle of November until the end of March. Fat, protein and specific energy declined greatly in winter but were replenished rapidly in spring. Rates of decline were slower for the smallest fish, which also had the lowest specific content of fat, protein, and energy, while the differences in absolute amounts were greatest for the largest fish. The mean specific fat content was reduced by 45–70% during winter, relative to the pre-winter period (September). Mean daily reductions in specific enegy of the larger size groups of brown trout (3·7 × 10⁻³ kJ g⁻¹ day⁻¹) were almost half of the corresponding values for the largest Atlantic salmon (6·3 × 10⁻³ kJ g⁻¹ day⁻¹) during winter. A minor reduction in protein content was found during winter, with mean reductions of 6–10% in comparison to those in September. During spring the fat content was replenished rapidly, particularly for the smallest salmon fry (a threefold increase from April to June). Fat content in the larger salmon and trout increased by about 1·8 times. Based on estimated metabolic rates, digested energy during wintertime may contribute about two-thirds of the brown trout fry's energy demand. For Atlantic salmon, the corresponding value is about 50%. The winter period put considerable stress on the young salmonids living in lotic environments, in particular for the smallest fry with the lowest energy content before winter and the largest losses during winter. This should make the fry more vulnerable to adverse abiotic and biotic factors.     

HOMING BEHAVIOR OF JUVENILE NORTHERN ELEPHANT SEALS

The aim of this study was to determine if juvenile northern elephant seals, Mirounga angustirostris , translocated from their rookery would return to it quickly and reliably. During the spring and fall of 1990 and 1991 we captured 75 seals at Año Nuevo State Reserve, CA, U. S. A. and translocated them to release sites up to 100 km away. Eighty-eight percent of the seals returned to the capture site within 4.7 ± 4.3 d. Homing rate increased with age, but even the youngest seals (8–10 mo) homed at a 73% rate. Homing rate did not vary significantly with sex, season, or year. Data from diving instruments suggested that the seals often followed direct routes home, arrived on the rookery significantly more often at night than during the day, and when released together, returned separately. Mean homing speed of 18 seals with complete diving records was 39 km/d (range 3–70 km/d). Instruments on seals had no detectable effect on homing rate or homing speed. The translocation paradigm provides a powerful tool for conducting intensive shortterm studies on free-ranging seals.     

Fish production in the Jarama River, Central Spain

Fish production was estimated at three sites on the Jarama River, a small, typical upland river in Central Spain. Population estimates were made by the successive removal method of electrofishing. The same six species were recorded at each of the sites: Chondrostoma polylepis, Barbus barbus bocagei, Leuciscus cephalus pyraenaicus, Salmo trutta m. fario, Gobio gobio and Cobitis paludicola , with the first three species always dominant. Density, biomass, production (assuming that N_o is the total number of eggs spawned), and available production were, respectively: 13502-85776 ind. ha⁻¹, 178.6–221.3 kg ha⁻¹, 221.7–583.6 kg ha⁻¹ yr⁻¹, 118.1–271.9 kg ha⁻¹ yr⁻¹. Production estimates based on mortality curves were 7.9–19.5% (mean: 13.7) lower than those based on estimated from the number of eggs laid. Production per unit of area was highest at the widest and deepest site. Brown trout production contributed only 2–4% of the total production for all sites.     

Bioelectronic monitoring of parasite-induced stress in brown trout and roach

A non-contact bioelectronic monitoring system was used to record changes in heart rate, ventilation rate and swimming activity in brown trout Salmo trutta and roach Rutilus rutilus , following exposure to two species of cercariae of digenean trematodes: Diplostomum pseudospathaceum which is a common parasite in the lens of fishes and xiphidiocercariae of Plagiorchis elegans , a parasite of anatid birds, both of which have the snail Lymnaea stagnalis as their first intermediate host. Swimming activity increased significantly in roach exposed to Diplostomum cercariae at densities as low as 3.8l⁻¹ and remained elevated for 24–36 h post exposure. Brown trout showed no response when exposed to low densities of Diplostomum (2.9 and 5.7 cercariae 1⁻¹) but there was a significant response at higher cercarial exposure densities (>501⁻¹). Total activity of brown trout increased immediately, peaking after 2 h and returning to pre-exposure levels within 5–6 h. There was a simultaneous increase in heart and ventilation rates which both declined following the reduction in activity of the fish. Heart rate then increased for a second time to a maximum level at 14–16 h and thereafter declined to reach a steady state at 3 days post-exposure. During this period there was no significant change in total activity. The qualitative nature of the heart response was identical in five infected brown trout although the magnitude of the response varied widely among fish. Exposure to cercariae of P. elegans elicited no response in either fish species. (c) 1996 The Fisheries Society of the British Isles     

The growth of juvenile Atlantic salmon, Salmo salar L., and brown trout, Salmo trutta L., in a Scottish river system subject to cooling-water discharge

The River Fiddich, a tributary of the R. Spey in north-east Scotland, is a spawning river for both Atlantic salmon and brown trout. Warm cooling water effluent is discharged from several distilleries at different points in the lower reaches and raises the temperature of the river 1–3°C above ambient for most of the year. Salmon and trout grow more rapidly in this region than further upstream, and juvenile salmon generally migrate a year earlier, as 2 + smolts. Available data were too few to determine whether there was a similar difference for trout. Similar studies on the R. Dullan, a tributary of the Fiddich, and on the Cromdale Burn in the same area, confirmed that the growth rate of fish is faster downstream from distillery discharge points. It is suggested that increased invertebrate production may influence the growth rate.     

Pools as refugia for brown trout during two summer droughts: trout responses to thermal and oxygen stress

In non–drought years (1977, 1985), temperatures and oxygen concentrations from 1 to 14 July at the deepest point in each of five pools in Wilfin Beck were similar with ranges of 12–18° C and 7·8–9·8 mg l^–1. Trout Salmo trutta were present in all pools. In drought years (1976, 1983), temperature increased and oxygen concentration decreased as pool size decreased. In the two smallest pools, they were outside the thermal and oxygen limits for trout (ranges for both pools 24–29° C, 1·2–2·5 mg l^–1), and trout were absent. Values in a medium–sized pool were close to the incipient lethal levels and a few juvenile trout were present in both drought years. The lowest temperatures and highest oxygen concentrations were recorded in the two largest pools (ranges 20–25° C, 3·6–4·8 mg l^–1) and trout of all ages (0+ to adults) were present in both drought years. In these two pools, both temperature and oxygen concentration decreased from the surface to the deepest point in the pool. Trout preferred lower temperatures near the pool bottom rather than higher oxygen concentrations near the surface, but some fish moved towards the surface at night when the pool cooled slightly. These field results were discussed in relation to lethal values recorded for brown trout in the laboratory, and there was general agreement between field and laboratory values. Trout in the drought years occurred at temperatures close to, or below, the incipient lethal value of 24·7° C (+0·5) and also at the highest oxygen concentrations, but only when these were at temperatures below the incipient lethal value.