The smolt run and postsmolt survival of Atlantic salmon, Salmo salar L., in relation to early summer water temperatures in the northern Baltic Sea

Abstract –  The timing of the smolt migration of Atlantic salmon, Salmo salar L., was investigated during 1972–2002 in the Simojoki, a river flowing into the northern Baltic Sea. The onset of the smolt run was positively correlated with the river water temperature; a rise in water temperature above 10 °C being the main proximate environmental triggering factor. There was also a weaker correlation between the decreasing river discharge in the spring and the onset of the smolt migration. The duration of the main run was shorter in the years when the onset of the smolt run was delayed. No differences were found in the onset timing or in the duration of the smolt run between wild smolts and semi-wild smolts released into the river as parr. A polynomial equation fitted to the annual data on the survival of Carlin-tagged wild smolts and the sea surface temperature (SST) in June off the river mouth appeared to follow a dome-shaped pattern. Survival was lower in cold early summers (SST <9 °C) than in those with an average SST (9–11.9 °C), and lower again, although not significantly, in warm early summers (SST ≥12 °C). Too low and probably also too a high water temperature in early summer could thus be one of the underlying reasons for the fluctuations observed in postsmolt survival in the Baltic Sea.     

The prevalence of escaped farmed salmon, Salmo salar L., in the River Ewe, western Scotland, with notes on their ages, weights and spawning distribution

Abstract  The prevalence of escaped farmed Atlantic salmon, Salmo salar L., in the River Ewe, western Scotland, was assessed. After the establishment of smolt cages in the catchment and marine cages near the river mouth during 1986–1987, approximately 425 000 parr and smolts, and 122 000 growers have escaped. Between 1987 and 2001, farmed salmon occurred in the rod fishery in 13 of the 15 years, contributing at least 5.8% of the total catch, with a maximum annual frequency of 27.1%. It was estimated that <1% of fish escaping from the marine cages entered the river, but contributed at least 27% of potential anadromous spawners in 1997. Radiotagged, farmed fish in 2001 probably spawned in three subcatchments also used by tagged wild fish. Despite the likelihood of hybridisation there was no change in the median weight or marine age of wild fish, but smolt age decreased significantly ( P  < 0.02). The Ewe has a depleted wild salmon population (≤900 anadromous adults), and further genetic introgression by escapees should be prevented.     

Density of Atlantic salmon, Salmo salar L., smolts in the river Orkla, a large river in central Norway

Abstract. Estimates of Atlantic salmon, Salmo salar L., smolt density were conducted in the river Orkla, central Norway, in spring 1983 by tagging 2671 smolts. The fish were captured in three sections of the river and marked by cutting the fins. Smolts larger than 110 mm were separated from fish between 100 and 110 mm, resulting in four series of markings. During the smolt run, 1285 smolts were captured in two traps lowered from a bridge, situated downstream of the area of the river where the fish were tagged. The recapture of tagged smolts was 27 specimens (1%). varying between 0·8% and 1·2% for the different series of markings. The estimated smolt densities varied between 2·8 and 4·4 smolts per 100 m2 from the four markings, with 4·1 smolts per 100 m2 (95% confidence interval 2·8–6·1) based on the total number of recaptures.     

Predation by cormorants, Phalacrocorax carbo (L.), on the salmonid populations of an Irish river

Abstract. Counts were made of cormorants, Phalacrocorax carbo (L.), feeding on the River Bush. County Antrim. Northern Ireland during the post-dawn period on three occasions. Two of the counts during May 1986 indicated that up to 264 birds may have been feeding at least once per day throughout the catchment during the salmon, Salmo salar L., smolt run. The number of feeding birds had dropped to an estimated 61 by the time of the third count on 1 July 1986. Stomach samples from shot birds showed that upstream feeding was concentrated on wild smolts and brown trout. Salmo trutta L. However, cormorant predalion downstream from the salmon hatchery at Bushmills was restricted solely to hatchery smolts. Estimates of the total daily predation rates were calculated at 653–1214 wild smolts. 107–231 hatchery smolts and 422–785 brown trout. The possible impact of this level of predation on the salmonid stocks of the river was assessed.     

Survival of migrating sea trout (Salmo trutta) and Atlantic salmon (Salmo salar) smolts negotiating weirs in small Danish rivers

Abstract – The survival of brown trout and Atlantic salmon smolts during passage over small weirs was estimated in two small Danish rivers during the spring of 1998. Parallel groups of smolts were released upstream and downstream of the weirs and recaptured in traps further downstream. The results showed a smolt loss varying from 18 to 71% for trout and 53% for salmon. Furthermore, the surviving smolts from the upstream groups were delayed for up to 9 days compared to downstream groups. The study demonstrated that an increased proportion of total river discharge allocated to fish passage increased the smolt survival. Losses may be because of fish penetrating grids erected at fish farm inlets, predation and delays, which may lead to desmoltification. The low survival may seriously threat both the long-term viability of wild populations of anadromous salmonids and the outcome of the intensive stocking programme in Denmark.     

Long-term changes in the smolt size and age of Atlantic salmon, Salmo salar L., in a northern Baltic river related to parr density, growth opportunity and postsmolt survival

Abstract –  The size of wild Atlantic salmon ( Salmo salar L.) smolts in 1972–2004 was studied in relation to parr density, smolt age, growth opportunity and postsmolt survival in the Simojoki River. There was a significant negative regression between the annual mean smolt size and the density of wild >1 year parr in the previous autumn, but not between the annual mean smolt size and age. The density of reared parr released into the river or the growth opportunity, based on the day length and air temperature during the previous summer, did not affect the size of wild smolts. The data on postsmolt survival based on recaptures of Carlin-tagged smolts showed a significant positive relationship ( P  < 0.01) between the survival of postsmolts and the annual size of wild smolts. It is hypothesised that the increased density of wild >1 year parr could have contributed to the decreased smolt size since the 1990s, and the reduced size of wild smolts could be included among the factors resulting in their declined postsmolt survival in the Baltic Sea.     

Differences in sea migration between wild and reared Atlantic salmon (Salmo salar L.) in the Baltic Sea

The effect of origin, smolt size and year of release on the sea migration pattern of Atlantic salmon (Salmo salar L.) in the Baltic Sea was examined by tagging experiments conducted in 1991–1993 on wild and reared smolts of the Simojoki river salmon stock. The tag recovery data analysed by log-linear models revealed significant differences in both spatial and temporal sea migrations between the wild and reared salmon; the variation was attributed to the year of release and to the origin of the fish. Grilse accounted for the majority of reared returners (76%) but for a smaller proportion (46%) of the wild fish. The effect of smolt size could be studied only in the smolt groups tagged in 1991. Wild fish were more frequently (71%) caught in the Baltic Main Basin than were reared fish (51%) during their second sea year, and the size variation between wild and reared smolts did not explain the recovery site. No such differences in spatial distribution were found during the third sea year. The tagging place (hatchery/trap) of the reared fish did not affect their later sea migration. The differences in sea migration patterns suggest that the wild salmon are more vulnerable to the intensive salmon fishery in the Baltic Main Basin than are reared fish.     

Effect of smolt age on migratory behaviour of Baltic salmon, Salmo salar L., transplanted to the east Atlantic

Abstract. This paper describes tests which were made to determine if smolt age at release influences the migratory pattern of three different stocks of salmon, Salmo salar L. The fish were hatchery-reared and released in two different rivers, the River Imsa and the River Akerselv. Based on the tag returns we found that Baltic salmon from the River Neva, USSR differed in migratory pattern from two Norwegian stocks from the River Lone and the River Imsa. A large proportion of the 2+ River Neva smolts stayed in the fjord during the summer and autumn after release. On the other hand, 2+ smolts of the Norwegian stocks left the fjord and migrated to the feeding areas in the Norwegian Sea within a short time after release. The 1+ smolts of all stocks showed the same migratory pattern as the 2+ smolts of Norwegian origin. We propose that the observed differences in migratory pattern are influenced by the developmental rate of the smolts. The effect of developmental rate on the migration may differ among stocks. Our results show that it is possible to develop a fjord fishery by releases of 2+ smolts of Neva salmon. However, such releases must be carried out with the utmost caution, preferably in fjords with no salmon rivers, so that the possibility of gene flow between populations is minimized.     

Estimates of the annual loss of Atlantic salmon, Salmo salar L., in Norway due to acidification

Abstract. The pre-acidification level of Atlantic salmon, Salmo salar L., production in Norway was estimated from accessible rearing habitat, potential smolt production, smolt to adult survival, and mean adult weight. Atlantic salmon have been virtually lost in 25 rivers due to acidification. In total, 340.6km of river is affected, and this corresponds to a rearing area of 2044.8 ha. The total annual number of adult salmon lost was estimated to be between 92016 and 306720 individuals, weighing some 345-1150 tonnes.     

Content of synthetic astaxanthin in escaped farmed Atlantic salmon, Salmo salar L., ascending Norwegian rivers

Abstract  Isomeric ratios of astaxanthin in eggs and alevins of Atlantic salmon, Salmo salar L., have proven useful in identifying female spawners of farmed origin, but the method underestimates the proportion of fish of farmed origin. The rate of underestimation was studied by analysing astaxanthin content in tissue of 55 farmed Atlantic salmon ascending two Norwegian rivers in the autumn of 1991. The astaxanthin content fell into two distinct classes. Fifty-one per cent of the adult escaped salmon had isomeric ratios similar to salmon fed synthetic astaxanthin, whereas all the remaining fish had ratios similar to wild fish. Discriminant analysis classified 96.4% of the fish with known astaxanthin content into the correct astaxanthin class on basis of tail-fin erosion, length, weight and gill-cover damage. This discriminant function was used to estimate the astaxanthin classification of 1017 farmed salmon caught in nine rivers during 1989–1991. The classification success varied among years from 52 to 64%. Corresponding numbers for females and males were 45–48% and 54–70%, respectively. Thus, estimates of spawning rates of farmed female salmon via astaxanthin content in eggs or alevins from redds should be adjusted accordingly. The observed isomeric ratios of astaxanthin in the escaped farmed salmon and the relationship with morphology indicates that a significant proportion of the escapees ascending rivers have spent more than 1 year in the wild after escape.     

Strontium levels in scales and vertebrae of wild and hatchery-reared Atlantic salmon, Salmo solar L., smolts

Abstract. Analyses of the Sr-contenl in scales of Atlantic salmon, Salmo saiar L ., smolts from two hatcheries revealed significant ( P < 0·001) differences. These differences were reflected in the Sr-conients of their respective diets. Sr-values in scale samples taken from wild salmon smolts from 10 Norwegian rivers showed a considerable variation. Analysis of variance showed that sampling site was the major source of variation. In general the Sr-content in scales cannot be used to distinguish between hatchery-reared and wild salmon smolls, although the present results nevertheless suggest that such a distinction is possible in some localities.
The Sr-contenl of the vertebrae was somewhat lower than that of the scales in both hatchery-reared and wild smolls. The Sr-conient of the scales of sea trout, Salmo trutta L., smolts from one of the sampling sites was significantly ( P < 0·001) higher than that of scales of Atlantic salmon smolts from the same site. The Sr-content of the scales of all the salmon smolts sampled from a lake was higher than the values recorded for sea trout and salmon after their stay in the sea. Use of the Sr-contenl of the scales todistinguish between migratory and resident individuals should therefore be done with care.     

Homing patterns of Baltic salmon, Salmo salar L., from smolts released from two hatcheries in the River Dalälven, Sweden

The River Dalälven Baltic salmon, Salmo salar L., population has been maintained by stocking reared fish since the early 1920s. Initially, all rearing was carried out at one hatchery, but since the late 1980s two have been used. Both hatcheries are situated 9–10 km from the river mouth but some 600 m apart. All broodfish were caught in a single fish trap situated some 700 m upstream of the upper hatchery. The salmon smolts were released just below the water outlets of each hatchery, respectively. About 2% of the released smolts from each hatchery were tagged annually with Carlin tags. Total recapture rates were higher for smolts from the lower hatchery. A higher proportion of recaptured fish was reported from the home river for salmon from the upper hatchery. The migration within the river to the fish trap was more precise for fish from the upper station. Strays were very late in the season and of a higher number from the lower hatchery. Observations of jumping salmon by the outlet from the lower station indicated that salmon returned to that point. The lower recaptures in the trap were considered a result of a shorter river migration of salmon from the lower hatchery.     

Reduction of brown trout, Salmo trutta L., salmon, S. salar L., and rainbow trout, Oncorhynchus mykiss (Walbaum), smolt bycatches in eel pound nets

Two types of bycatch reduction devices (BRDs) were tested in the Randers Fjord, Denmark, aimed at deflecting the surface-oriented smolts of brown trout, Salmo trutta L., salmon, Salmo salar L., and rainbow trout, Oncorhynchus mykiss (Walbaum), before they became trapped, while retaining the catches of eel, Anguilla anguilla (L.). The methods tested were: a) placing a floating guard net between the wings; and b) submerging the pot net (i.e. last enclosure before fyke net) 55–100 cm below mean sea level. After each haul the pound net-setups were changed from the control to one of the types of BRD, and vice versa. Both methods significantly reduced the bycatch of brown trout smolts, while catches of legal-sized eels were not affected. Submerging the pot net reduced smolt catches of all species; mean reductions were 91.1% for brown trout, 74.5% for rainbow trout, and 86.1% for salmon.     

Delayed smolt migration of stocked Atlantic salmon parr

Abstract The timing of the smolt run in the Dale River in western Norway was monitored from 2002 to 2007 after annual stocking in late autumn 2000 to 2005 with 5000–10800, 11–16 g, Atlantic salmon, Salmo salar L., parr. The releases yielded an annual smolt production of 1000–2000 individuals, mainly 1+ smolts. Almost 5700 stocked smolts were trapped during smolt migration and 60% of these were genotyped for family identification. The date for 50% descent varied by 14 days from year to year. For the most part, however, the 2+ stocked smolts and the majority of the wild smolts left the river in May, while the 1+ stocked smolts migrated 23–26 days later in June. It was concluded that the strategy of stocking large parr in late autumn may conflict with the natural timing of smolt migration the following spring.     

Relationships between marine growth and marine survival of one sea winter Atlantic salmon, Salmo salar L., from the River Bush, Northern Ireland

An examination of marine growth/marine survival relationships in Atlantic salmon, Salmo salar L., was carried out, based on scale growth measurements in relation to two indices of marine survival in wild fish from the River Bush, Northern Ireland. The survival of cohorts to the Irish/Northern Irish coast (prefishery) and to fresh water was statistically unrelated to variation in growth from smolt migration to the end of the first winter at sea ( P  > 0.1; – P  > 0.7). Marine growth of 1+ smolts decreased significantly during the period of the study ( P  < 0.05), but growth of 2+ smolts did not change ( P  > 0.05). The variability in marine growth was much less than the variation in natural survival at sea, suggesting that factors instead of or in addition to, growth influence natural survival in the marine environment. Survival to fresh water was not related to survival to the coast ( P  > 0.4), although it was inversely correlated with exploitation rate ( P  < 0.01). These results are discussed in relation to the use of freshwater returns to assess marine survival and the potential for the variation in natural marine mortality to influence total life-cycle variation.     

Early marine survival and movements of escaped Atlantic salmon Salmo salar L. juveniles from a land‐based smolt farm during autumn

The aim of this study was to examine early marine survival and movements of simulated escaped Atlantic salmon Salmo salar L. pre‐smolt and smolt from a commercial smolt farm during autumn. One‐third of the pre‐smolt most likely died in the immediate vicinity of the release location, whereas the corresponding mortality for smolts was lower (8.5%) during the 5‐week study period. The surviving pre‐smolt left the farm area after 2–3 days, predominantly along the shore. In contrast, most of the surviving smolts left the farm area during the first day and 54% seemed to move away from the shore and adopt a more pelagic movement pattern than pre‐smolt. The number of surviving fish recorded in the fjord decreased throughout the study period, possibly due to a combination of fish migrating out of the fjord or undetected mortality. Compared with existing knowledge on migration of released farmed smolts during spring, our results indicate less directional and slower movement rates during autumn. Only two of the tagged fish were detected upstream in the rivers following release. A rapid dispersion of escapees indicates that the potential for recapturing escapees is limited unless recapture efforts are initiated immediately after escape. Hence, there is a need for development of technology that detects and prevents escapees to enter the sea.     

Seasonal differences in smolt traits and post-smolt survival of wild Atlantic salmon, Salmo salar, migrating from a northern boreal river

Abstract  Seasonal differences in smolt traits and the post-smolt survival of wild Atlantic salmon, Salmo salar L., were investigated by smolt trapping and Carlin-tagging in the River Simojoki, northern Finland between 1991 and 2004. The annual trapping season was divided into two halves based on the median catch date. Smolt length was significantly higher during the first half of the season, while differences in smolt weight were typically small. Smolt age was always significantly higher during the first half of the season because older smolts tended to migrate earlier in the season. Many smolts migrating during the early season and almost all smolts migrating later had started their new growth, indicating that smolts grow in the spring before sea entry. The differences in recaptures between smolts tagged during the first and second halves were insignificant. Although variations in smolt traits and environmental conditions can produce inter-annual variation in post-smolt survival, their seasonal differences seem to be too small to have an effect.     

Inter-stage survival of wild juvenile Atlantic salmon, Salmo salar L.

A biological model was developed to calculate annual survival between life stages of juvenile Atlantic salmon, Salmo salar L., in Catamaran Brook, a small stream basin (52 km²) in the Miramichi River catchment in New Brunswick, Canada. Seven years’ data (1990–1996) were used in the model. Input variables included: daily fish counts and measurements of parr (3–4 age classes), smolts, and adult salmon at a fish-counting fence near the stream mouth; biennial quantification of all habitat types along the watercourse; fish density estimated by electric fishing at 30 sites; and estimates of young-of-the-year emigration via stream drift. Continuous recording of stream discharge provided data to assist in interpretation of survival estimates. Annual survival for juvenile salmon in their first 3 years of life in the stream averaged between 31% and 34%. The greatest annual variation (CV = 0.699) occurred at the egg to 0+ (summer) stage with a low of 9.2% survival recorded for a winter with an atypical midwinter flood event; parr and pre-smolt survival were similarly affected. Survival from egg deposition (after correction for losses caused by predation and retention/non-fertilization) to smolt emigration was between 0.16% and 0.52%, which is low relative to estimates from many other studies. Survival of smolts to returning 1-sea-winter adults (grilse) averaged 8.5%. Potential errors in the computation of the model are discussed, e.g. inaccurate counts of spawning adults during high autumn stream flow. A possible explanation for the low egg to smolt survival was the environmental conditions experienced during various winters. Mean egg survival was 1.3 times higher (39.3%) and egg to smolt survival increased to 1.03% when the two winters characterized by extremely low discharge or midwinter freshets were excluded from the calculation. Density-dependent factors related to a beaver dam, which limited spawning distribution, may also have contributed to poor survival and increased fry emigration in one year. Environmental factors, particularly winter conditions, in streams such as Catamaran Brook may act as bottlenecks to natural production of Atlantic salmon.     

Movements of two strains of radio tagged Altlantic salmon, Salmo salar L., smolts through a reservoir

Smolt migration through a shallow and turbid hydro-reservoir in a major Danish river system was investigated using radiotelemetry. Hatchery-reared 1+-year-old Atlantic salmon, Salmo salar L., smolts of equal size from two different non-native strains were radio-tagged and followed during their downstream migration through the 12-km-long reservoir. A total of 50 salmon smolts, 25 of Swedish (Øtran River) and 25 of Irish (Burrishoole River) origin, were surgically implanted with miniature radiotransmitters. The tagged smolts were tracked daily over a 3-week period in May 1996. The Øtran smolts initiated migration first ( P  < 0.001), moved faster ( P  < 0.01), were delayed less when passing a culvert ( P  < 0.001) and were more successful in moving through the reservoir than the Burrishoole smolts. The observed differences in migratory behaviour are interpreted as evidence of a genetic component influencing smolt migration.     

The straying of Icelandic ranched Atlantic salmon, Salmo salar L.: release and recapture techniques

The straying rate of ranched Atlantic salmon, Salmo salar L., into rivers in Iceland was estimated on the basis of coded wire tag recoveries. Out of a total of 15 158 recaptured tagged salmon from the releases between 1987 and 1992, 189 fish (1.3%) strayed into 25 out of the 79 salmon rivers observed. Most of the strayers were found in neighbouring rivers to the ranching stations. There were no significant differences in straying rate between different age classes of salmon returning from the same smolt year class. Generally, there was a delay of 26-27 days in running time between strayers in rivers and salmon returning to the ranching station. Higher straying rates were observed for ranching stations using riverine traps than for stations using estuary traps. By close inspection of seven key rivers in Iceland and assuming a 50% exploitation rate (fishing effort) in the rivers, on average, 2.1% of the returning salmon in ranching were estimated to stray to native salmon rivers over the years. A limitation of using these numbers to estimate geneflow between ranching stocks and wild populations is discussed.