Gill chloride cell surface-area is greater in freshwater-adapted adult sea trout (Salmo trutta, L.) than those adapted to sea water

An increase in the apical surface-area exposed to the environment in sea trout ( Salmo trutta , L.) branchial chloride cells, examined by scanning electron microscopy after adaptation to fresh water, indicates that salt-uptake may be dependent upon apical membrane morphology.     

Change in allometric length–weight relationship of Salmo trutta at emergence from the redd

In their life cycle, especially at early life stages, fishes pass through distinct growth stanzas with different length‐weight relationship patterns. Salmonid fish fry emergence from the redd gravel is a crucial moment in their life history. This study presents an ontogenic change in allometric length–weight relationship scaling of sea trout Salmo trutta at the time of emergence from the natural redds in a small lowland stream of western Lithuania. The paper also gives shrinkage rates and correction factors for emergent Salmo trutta fry after protracted formalin preservation.     

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.     

Induction, isolation and a characterization of the lipid content of plasma vitellogenin from two Salmo species: rainbow trout (Salmo gairdneri) and sea trout (Salmo trutta)

Vitellogenin synthesis is induced in juvenile rainbow trout (Salmo gairdneri) and juvenile sea trout (Salmo trutta) by estradiol-17 beta. A purification procedure for vitellogenin from trout plasma by precipitation with MgCl2-EDTA and subsequent anion exchange chromatography on DEAE-Sephacel is described. The total lipid contents of purified rainbow trout and sea trout vitellogenins are 18 and 19%, respectively. Approximately 2/3 of the lipids are phospholipids, while the remainder consists of triglycerides and cholesterol. Phosphorus determinations on delipidated vitellogenin yield a phosphorus content of 0.63% in rainbow trout and 0.58% in sea trout vitellogenin. Native (dimeric) vitellogenins from rainbow trout and sea trout both have an apparent molecular weight of 440,000, when estimated by gel filtration on Sepharose 6B.     

The pathology and seawater performance of farmed Atlantic salmon infected with glochidia of Margaritifera margaritifera

The pathology of glochidial infection of the freshwater mussel Margaritifera margaritifera was examined in farmed Atlantic salmon Salmo salar in fresh water and for 150 days after transfer of salmon to sea water. Prevalence of infection in fresh water was 95%, mean abundance 134 per fish and mean infection intensity 140. Prevalence in sea water was 80–94% in the first 7 weeks after transfer but glochidia were absent, apart from remains, after 50 days in sea water. Glochidia on salmon in fresh water were associated with localized hyperplasia and fusion of secondary gill lamellae. Focally extensive epithelial hyperplasia and fusion of secondary lamellae were present 4–10 days after transfer to sea water. Twenty-three days after transfer, small nodules with a more discrete appearance were present suggesting partial resolution of tissue response; hyperplastic responses associated with glochidia were much reduced after 50 days. Plasma chloride in infected fish 10 days after transfer was 153 mmol. 1⁻¹, significantly higher than fish without infection, suggesting poorer adaptation to sea water. No mortalities due to glochidial infection in sea water were recorded and there was no significant difference in mean weight between infected and control fish.     

Migratory timing, marine survival and growth of anadromous brown trout Salmo trutta in the River Imsa, Norway

The aim of the paper was to study sea migration, growth and survival of brown trout Salmo trutta of the River Imsa, 1976–2005. The migratory S. trutta were individually tagged and fish leaving or entering the river were monitored daily in traps located near the river mouth. The mean annual duration of the sea sojourn was 6–9 months for first-time migrants moving to sea between January and June. It was 8–18 months for those migrating to sea between July and December. Veteran migrants stayed 12 months or less at sea and most returned to the river in August. Early ascending fish stayed the longest in fresh water because most returned to sea in April to May. The day number of 50% cumulative smolt descent correlated negatively with mean water temperature in February to March and the February North Atlantic Oscillation index (NAOI). Mean annual sea growth during the first 2 years after smolting was higher for S. trutta spending the winter at sea than those wintering in the River Imsa. First year's sea growth was lower for S. trutta descending in spring than autumn. For first-time migrants, it correlated negatively with the February NAOI of the smolt year. Sea survival was higher for spring than autumn descending first-time migratory S. trutta with a maximum in May (14·9%). Number of anadromous S. trutta returning to the river increased linearly with the size of the cohort moving to sea, with no evidence of density-dependent sea mortality. Sea survival of S. trutta smolts moving to sea between January and June correlated positively both with the annual number of Atlantic Salmo salar smolts, the specific growth rate at sea, and time of seaward migration in spring. This is the first study indicating how environmental factors at the time of seaward migration influence the sea survival of S. trutta .     

Population and size-specific distribution of Atlantic salmon Salmo salar in the Baltic Sea over five decades

Population-specific assessment and management of anadromous fish at sea requires detailed information about the distribution at sea over ontogeny for each population. However, despite a long history of mixed-stock sea fisheries on Atlantic salmon, Salmo salar, migration studies showing that some salmon populations feed in different regions of the Baltic Sea and variation in dynamics occurs among populations feeding in the Baltic Sea, such information is often lacking. Also, current assessment of Baltic salmon assumes equal distribution at sea and therefore equal responses to changes in off-shore sea fisheries. Here, we test for differences in distribution at sea among and within ten Atlantic salmon Salmo salar populations originating from ten river-specific hatcheries along the Swedish Baltic Sea coast, using individual data from >125,000 tagged salmon, recaptured over five decades. We show strong population and size-specific differences in distribution at sea, varying between year classes and between individuals within year classes. This suggests that Atlantic salmon in the Baltic Sea experience great variation in environmental conditions and exploitation rates over ontogeny depending on origin and that current assessment assumptions about equal exploitation rates in the offshore fisheries and a shared environment at sea are not valid. Thus, our results provide additional arguments and necessary information for implementing population-specific management of salmon, also when targeting life stages at sea.     

Tolerance to gas supersaturation in fresh water and sea water by steelhead trout, Salmo gairdneri Richardson

The euryhaline status of steelhead trout, Salmo gairdneri , smolts was challenged in sea water for 2 weeks after which half of the total fish population was returned to fresh water. Acclimation continued and created two test populations in 29%osea water and fresh water. Subsequently these fish were exposed in fresh water or sea water to approximately equal hyperbaric dissolved total gas pressures (ΔP) of 190 mm Hg or about 125% of barometric pressure. Sea water was easier to supersaturate with air and required only about 10% of the entrained air which was required in fresh water at the same temperature and pressure. Mean time to first mortality was sooner in sea water. Mean times to mortality (10–50%) were not significantly different between fresh water and sea water, but there was a noticeable trend for longer survival in fresh water.     

Seasonal occurrence of sea lice Lepeophtheirus salmonis on sea trout in two north Norwegian fjords

Seasonal occurrence of the parasitic copepod Lepeophtheirus salmonis (sea lice) was studied from March to December 2001 in two large north Norwegian sill fjords without fish farming activity, the Ranafjord and the Balsfjord. Anadromous brown trout Salmo trutta (sea trout) in both fjords had a low infestation rate during all sampling periods, but followed a seasonal pattern. During early and late winter (November to December and March to April) and spring (May to June), the prevalence varied from 0 to 25% and the abundance was <0·5 sea lice. Adults dominated (92%) during this period, particularly gravid females. In both fjords, the highest prevalence was during September (80–81%, all stages represented). In Ranafjord, the abundance and mean intensity during this month was 6·8 and 8·6 sea lice, respectively, while in Balsfjord it was 3·6 and 4·5 sea lice, respectively. Fish were captured at temperatures down to 1° C and at full strength sea water which is supposed to cause osmoregulatory problems for the fish. This observation has implications for the understanding of high‐latitude sea trout behaviour and can also make the fish more vulnerable to heavy sea lice infestation during this period. It is suggested that winter running sea trout help to maintain a self replicating local population of sea lice within such fjord systems where other possible hosts ( e.g . farmed Atlantic salmon Salmo salar ) are not present during a whole year cycle.     

Adaptation of trout to seawater. Effects on sodium plasma concentration, gill exchange and intestinal transport]

10. Trout Salmo irideus are adapted to sea water (S W) within four weeks by submitting them to a stepwise increase in external salinity (successively: 1/3 SW, 1/2 SW, 3/4 SW, full SW). 20. In completely adapted individuals mean plasma electrolyte concentrations vary only slightly (by a few %) from one medium to another. Thus, the trout may be regarded as a euryhaline, eventually homeosmotic species. 30. With increasing outside salinity there is a progressive diminution in the overall gill permeability to ions which is suggested by saturation curves obtained for sodium fluxes (maximum at about 500 muEq/h. 100 g at 15 degrees C, for unshocked fish). 40. Disturbance of the animals provokes a striking elevation and desequilibrium in these exchanges and this in turn induces an abnormal rise in plasma concentrations and a subsequent failure to adapt to hypertonic media. 50. In vitro absorption of water and sodium by intestinal everted-sacs increases only after transfer to full sea water. Mucosal entry of ions into intestinal epithelial cells measured by the technique of Schultz et al. (1967), is diminished in sea water-adapted animal (by 42% in the case of sodium). 60. These results demonstrate that Salmo irideus possesses efficient osmoregulatory mechanisms which operate with minimal energy expenditure in hypertonic media.     

Survival and growth of sea trout parr in fresh and brackish water

There was no di.erence in survival or growth rate over 63 days for young-of-the-year sea trout Salmo trutta in fresh and brackish Baltic Sea water (6·7 psu). Hence, such sea trout parr that migrate from the freshwater habitat in which they hatch to the Baltic coastal zone, without smolting, should experience little or no physiological cost in survival and growth.     

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.     

Are long term negative effects from external tags underestimated? Fouling of an externally attached telemetry transmitter

An externally attached radio transmitter and antenna on a farmed Atlantic salmon Salmo salar was overgrown with green algae, mussels, seaweed and Balanus sp. after the fish had stayed at sea from December 1997-July 1998. This observation indicates that fouling may be an important factor, which is seldom considered when estimating negative effects from tags on the animals. Fouling increases the drag from the transmitter, and may affect the swimming speed, energy budget and behaviour of the fish. The effect is likely to be most pronounced in coastal waters.     

Mucous cell types in the branchial epithelium of the euryhaline fish Poecilia vivipara

On transfer to sea water for 45 days, the return of appetite was later and growth rates tended to be lower for triploid Atlantic salmon, Salmo salar , reared together with diploid Atlantic salmon. All mortalities comprised of triploid salmon (29%) and were attributable to failed smolt syndrome. No correlation was found between the growth of diploid or triploid fish in fresh water and their subsequent growth on transfer to sea water.     

Studies on the biology of Eubothrium salvelini and E. crassum in resident and migratory Salvelinus alpinus and Salmo trutta and in S. salar in North Norway and the islands of Spitsbergen and Jan Mayen

Samples of Eubothrium salvelini and E. crassum were obtained from resident and migratory Salvelinus alpinus and Salmo trutta and from S. salar at sea from North Norway and the islands of Spitsbergen and Jan Mayen. Scolex dimensions proved an unsuitable character for identifying these two parasite species, and use of alternative characters confirmed that E. salvelini is specific to Salvelinus and E. crassum to Salmo. Distributions of both species are co-extensive with their hosts, but levels of infection in any locality relate to the abundance of zooplankton. E. salvelini exhibits seasonal maturation and incidence cycles in char. It is recognised as being a freshwater parasite, although some individuals can survive the period of marine migration of sea char. Returning migrant char may contain such individuals together with small plerocerciform parasites acquired almost immediately upon their re-entry to freshwater. No evidence for marine infections with E. salvelini was found. The presence of plerocerciform and gravid adult E. crassum in salmon caught at sea confirms the existence of a marine life cycle and a marine race in this species. In salmon moving from one medium to the other the marine and freshwater races replace each other, but in sea trout, which spend shorter periods at sea, complete replacement may not occur and at any one time fish may harbour individuals of both races. Recognition of the existence of two races clarifies much of the confusion surrounding the biology of this species.     

Marine feeding of anadromous Salmo trutta during winter

Juvenile and adult anadromous trout Salmo trutta utilize the sea for feeding during the winter in the Skagerrak. This finding conflicts with the traditional view that anadromous trout overwinter in fresh water. Adults, just prior to spawning, were captured at sea in October to December, and spent fish were caught at sea from October to April, showing that the fish may leave the stream and move to sea just after spawning and spend the winter there. During mid‐winter (January to February), the feeding probability (chance of finding a fish with food in its stomach) increased markedly with increasing body length, with no similar effect during early and late winter (October to December and March to April). Among individuals with food in their stomach (72·5%), there was no evidence for variation in feeding intensity [stomach fullness = (mass of stomach content)(fish body mass)⁻¹] among early, mid‐, and late winter.     

Repetitive acceleration swimming performance of brown trout in fresh water and after acute seawater exposure

The effect of acute seawater exposure on repeated swimming performance of brown trout Salmo trutta was investigated by use of a constant acceleration test (CAT). In fresh water, swimming speed was attained regardless of previous exercise, whereas swimming speed in sea water was significantly reduced during consecutive exercise.     

Impact of live food on survival and growth of hatchery‐reared sea trout (Salmo trutta trutta L.) parr in the wild

Survival rates and growth parameters of hatchery‐reared sea trout (Salmo trutta trutta L.) fry were determined after stocking in the wild. The larvae were hatchery‐reared for 12 weeks in two groups: fry were fed either on live zooplankton and live chironomidae larvae (LFG), or fed a pellet diet (PFG). The survival rate and specific growth rates were higher in the LFG than in the PFG group. Most effective for hatchery‐reared fish intended for stocking was the natural, live feed. The mean number of chironomid larvae found in the stomachs of fish that were initially captured in the wild was significantly higher in the LFG than in the PFG group. The live diet supplied in the rearing period had a positive impact on the foraging skills of the sea trout fry and their survival in the wild after their release on 24 April 2010.     

Size and age of maturity of Atlantic salmon correlate with the North Atlantic Oscillation Index (NAOI)

Sea‐age at maturity of Atlantic salmon Salmo salar decreased with increasing values of the seasonal NAOI from February to April. Body mass increment from smolts to adults of one‐sea‐winter Atlantic salmon increased with increasing NAOI in May at the time when the juveniles moved to sea.