Timing of migration and changes in age structure of Atlantic salmon, Salmo salar L., in the River Frome, a Dorset chalk stream, over a 24-year period

During the last 24 years, the number of Atlantic salmon, Salmo salar L., migrating up the River Frome has varied between < 1000 and > 4000 fish per annum. Most parr become smolts at age 1+ and there are three main sea ages of salmon returning to the river. Each sea age shows a bimodal pattern of migration in the river. Primary migration times for 3-sea-winter (3SW) fish are spring and autumn, with 2SW fish and grilse (1SW) peaking in summer and autumn. Some 28.4% of 3SW and 6.9% of 2SW fish are previous spawners. Multi-sea-winter fish historically passed over the counter in all months of the year, but recently, their numbers have declined, as have total numbers of fish of all ages. There has been a fundamental change in the age structure of the population, with grilse increasing in proportion over the study period. Photographs of fish, taken for validation of the counter, showed a significant decrease in mean length of grilse, but an increase in mean length for 2SW and 3SW fish. Rod catch data support these findings.     

Effects of the Faroese long-line fishery, other oceanic fisheries and oceanic variations on age at maturity of Icelandic north-coast stocks of Atlantic salmon (Salmo salar)

Investigations were conducted on the effects of oceanic variations (as indicated by sea temperatures) and catches of the Faroese, Norwegian Sea and West Greenland salmon fisheries on the sea-age composition of Atlantic salmon (Salmo salar L.) from 22 Icelandic north-coast rivers. Catches of grilse in rivers were strongly correlated among the 22 rivers, as were the ratios of grilse caught to two-sea winter (2SW) salmon caught the next year. Four of the 22 rivers showed increasing ratios over time and three of these rivers, all in the northeast, had significantly higher mean ratios after the expansion of the Faroese fishery than before (P < 0.05). No evidence was found from ratios for the other 18 rivers to suggest that Faroese fishing was significantly depleting those stocks, even though 13 micro-tagged north-coast salmon had been recovered in the fishery in the 1988–1989 season. No evidence was found that Norwegian Sea or West Greenland fisheries affected stock composition. The mean April–May sea temperature prior to when the smolts enter the sea was significantly and positively related to ratios in eight of the 22 rivers. This result, along with frequent significant correlations in ratios among rivers, indicated that more rapid growth of smolts in their first summer may have increased grilse to 2SW salmon ratios on several rivers.     

The risk of individual fish being captured multiple times in a catch and release fishery

The proportion of angled Atlantic salmon Salmo salar L. being caught and released has increased. If individuals are repeatedly captured, this may have fish welfare consequences. Of 995 Atlantic salmon tagged during catch and release in eight Norwegian rivers, 10% were captured twice, while 3% were captured three times within the same fishing season. The probability that released salmon were captured again decreased with decreasing time left of the fishing season, decreased for larger‐sized fish and varied among rivers/years. Increased exploitation rates within the river, indicating an increased fishing pressure, strongly increased the probability that fish would be recaptured. However, the proportion of salmon caught a second time was much lower than the total exploitation rates in the same rivers (which was on average 46%). For fish tagged in the sea, the likelihood of being angled decreased with time since entering the river, which may explain why the recapture rates of caught and released fish were lower than the total exploitation rates.     

An assessment of the grilse error associated with reported salmon,Salmo salar L., catches from two rod-and-line fisheries on the River Spey,Scotland, UK

Abstract Catch returns are often analysed as a means of inferring the status of salmon stocks. One aspect of such analyses is the problem of grilse error (the misreporting of one-sea-winter salmon as multi-sea-winter salmon), which may have important consequences for the management of salmon stocks. Reported catches from two estates on the River Spey between 1982 and 1992 were compared with the sea ages of the fish determined from scale reading. Weight was an important factor in determining the reported sea age of salmon in catch returns; the relationship between weight and sea age in the reported catch remained relatively constant throughout the angling season. Analysis of the scale sample data, however, indicated that the relationship between weight and actual sea age changed through the angling season, grilse accounting for increasing proportions of all weight classes up to 10 lbs (4.5 kg) as the season progressed. Grilse error was an identifiable problem at both estates, resulting in grilse catches being underreported by over 20%.     

Historical changes in age structure of Atlantic salmon, Salmo salar L., in the River Eo, northern Spain

Abstract Variations in the age structure and number of Atlantic salmon, Salmo salar L., running into the River Eo in northern Spain were assessed from catch records of sport fisheries for the period 1949 to 1991. The analysis focused on two periods (1951–1960 and 1981–1991) for which more complete data on fish number, size and age were available. Over the whole period, no evidence for a decline in the total salmon run was found, but the last few years revealed significant changes in both the number and age structure of salmon caught. The catches were mainly composed of multi-sea-winter salmon, and this did not change from the 1950s to the 1980s as the proportion of grilse remained unchanged. However, since 1980, there was a marked decline in both the proportion of 3-sea-winter salmon (versus 2-sea-winter fish) and the frequency of previous spawners among the multi-sea-winter salmon. These changes were probably linked because most of the previous spawners re-entered the river as 3-sea-winter or older salmon. River age of salmon caught in the 1950s was low and constant (about 90% of the catch had smolted at one year) but the mean age of smolting increased in the 1980s.     

Recovery and re-establishment of Atlantic salmon, Salmo salar, in limed Norwegian rivers

A total of 21 acidified Norwegian rivers are now being limed to re‐establish or restore Atlantic salmon, Salmo salar L., stocks. Natural reproduction of Atlantic salmon was evident 1 year after the first year of liming in all rivers that had lost their native stocks (n = 9) except for one river. The density of fry (age 0+) developed significantly more rapidly in rivers that supported remnant stocks than in rivers that had lost their stocks, based on data 5 years after treatment. Nine of the study rivers were supplied with hatchery‐reared salmon, mainly unfed fry. Of the rivers with lost stocks, those which were supplied with fish had significantly higher densities than those that were not enhanced. On the other hand, rivers with remnant stocks that were supplied with fish had significantly lower densities of salmon fry than those that did not undergo such mitigation measures. In 2001, all limed rivers yielded 41.9 t of salmon.     

Snorkelling as a method for assessing spawning stock of Atlantic salmon, Salmo salar

Abstract  Reliability of underwater snorkel counts of adult Atlantic salmon, Salmo salar L., was analysed in the tributaries of the River Teno, close to the spawning period. In small (width 5–20 m) rivers, the replicated total counts of salmon were reasonably precise (CV = 5.4–8.5%), while in the medium-sized river (width 20–40 m) the precision of the counting method was considerably lower (CV = 15.3%). Low precision in a medium sized river was also observed in an experiment using marked live fish where the observation efficiency varied between 36.4% and 70.0%. In a small river, the detection efficiency of artificial fish silhouettes (test salmon) was almost perfect in pools (98%), but decreased in rapids (84%). Separate counts of males, females, grilse and large salmon were usually more variable than total counts, indicating that divers were more capable of locating a fish than properly identifying its sex and sea-age. The behaviour of adult salmon was favourable to conduct snorkel counts, as fish normally stayed still, or after hesitating, moved upstream (>95%of the cases) when encountering a diver. The high observation efficiency (>90%) and precision, favourable behaviour of salmon and congruence between snorkel counts and catch statistics in small rivers suggest that reliable data on Atlantic salmon spawning stock can be collected by snorkeling provided that the environmental conditions are suitable and the divers are experienced.     

Sex Ratio and Potential Fecundity of Atlantic Salmon (Salmo salar L.) Caught by Anglers on the Elorn River (Northern Brittany, France) during 1979 and 1980

Analysis of the sex ratio of angling Atlantic salmon catches from March to mid-June on the Elorn river in 1979 and 1980 showed a majority of females among the spring salmon population. Comparison between serodiagnostic technique and visual observations of gonads indicated that the former method provided a very low error margin for sex ratio determination on all females in the early stages of maturation and entering rivers. Study of sexual characteristics of spring salmon bearing copepod parasites or not indicated that fish entering freshwater would initiate a new stage of the ovogenesis process characterized by a failure of about 30% of the oocytes and a correlation between fecundity and size that did not exist at the time of the entry into freshwater.     

Relationships between oceanic conditions and growth of Chinook salmon (Oncorhynchus tshawytscha) from California, Washington, and Alaska, USA

We model age‐specific growth rates of Chinook salmon (Oncorhynchus tshawytscha) with two life‐history behaviors from Alaska (i. Situk and ii.Taku Rivers), Puget Sound, Washington (iii., iv. Skagit River), and California (v. Smith River) relative to oceanic conditions in those regions. By analyzing over 20 yr of biological and physical data from the NE Pacific downwelling, upwelling, and transition zones, we are able to determine the factors affecting growth across much of the species’ range and between life‐history behaviors. With scale increment data from returning fish, we use path analysis and partial least squares regression to quantify the relationships between growth and regional‐ and large‐scale oceanic conditions (e.g., sea level height, sea surface temperature, upwelling). Alaskan fish with both ocean‐ and stream‐type behaviors were fit best by the environmental data from the winter in Alaska waters. Specifically, coastal and gyre factors such as sea surface temperature, river flow, and Ekman pumping positively correlated to growth, indicating a productive and strong Alaska Current promoted growth. Growth of fish from California was fit by local factors such as increased upwelling, lower coastal sea surface temperature, and wind stresses during summer and spring, indicating a productive and strong California Current promoted growth. For Puget Sound, Washington, growth of fish that migrate to sea in their first year was generally negatively correlated to a strong California Current. Puget Sound fish that spend a year in freshwater before migrating to sea were modeled well with environmental data from their source region for the first 2 yr at sea and by data from Alaska waters in their third year at sea. Results suggest that conditions in which the transition zone is dominated by neither the Alaska nor California Currents are best for increased growth of Puget Sound fish.     

Interactive effects of life history and season on size‐dependent growth in juvenile Atlantic salmon

Size‐dependent growth (SDG) is an important process in structuring populations as well as determining life history outcomes. Despite its importance, there have been few investigations from observational studies focusing on the interaction between life history decisions and SDG. In this study, we used data on individually tagged Atlantic salmon from both the laboratory and the field to investigate differences in SDG among two life history groups, parr and smolts. In the laboratory, we found little evidence of SDG in parr but seasonally dependent SDG in the smolt group. Smolts showed at strong compensatory response over the winter months just prior to the smolt transformation window. In the field, we found little evidence of SDG early in ontogeny (i.e., age 0+ fall and winter). There was some evidence of depensatory growth (positive SDG) during the age 1+ spring among both life history groups that may reflect random habitat variation or the monopolisation of resources. After the age 1+ spring, we found that smolts were more likely to show a compensatory effect (negative SDG) than parr. This effect was strongest, as they approached the smolt window in the spring of their age 2+ year. These results suggest (i) SDG is common in Atlantic salmon; however, the form and extent of life history depends on (ii) season and (iii) life history. For individuals that adopt a smolt life history, trade‐offs between freshwater survival and sea survival may lead to a convergent growth pattern, as they approach the smolt migration window.     

High marine survival rates of sea‐ranched Atlantic salmon smolts (Salmo salar) that had previously matured as male parr

Abstract The growth and recapture rates of Atlantic salmon, Salmo salar L., smolts that had previously matured as parr were compared with those of immature siblings in a sea‐ranching experiment in western Norway. The smolts were the offspring of three river populations. They were individually tagged, transferred to cages in a small bay where estuarine salinity gradients had been established and released on four dates from mid‐May to early June after either 3 or 7 days of acclimatisation. The previously mature male parr (PMMP) were smaller than their siblings before release, but performed much better during their time in the sea. As grilse, they reached sizes comparable with the formerly immature fish, and their recapture rate was more than four times higher (8.6 vs 2.1%). This difference decreased somewhat during the following years because 0.85% of the immature fish and only 0.1% of PMMP were recaptured as multi‐sea‐winter salmon. The highly successful marine performance of the PMMP demonstrated that this life history strategy may be more flexible than previously believed.     

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.     

Migratory behaviour of adult wild and escaped farmed Atlantic salmon, Salmo salar L., before, during and after spawning in a Norwegian river

The migratory behaviour of adult wild and escaped farmed Atlantic salmon, Salmo salar L., before, during after spawning in the River Namsen, Norway, was analysed using radio telemetry. The fish were caught, radio tagged and released into the fjord between 7 and 25 km from the river mouth. A significantly higher proportion of wild (74%) than farmed (43%) salmon was subsequently recorded in the river. Wild salmon (33%) were more frequently captured in the sea and in rivers than farmed salmon (14%). The migration speed from release to passing a data logger 11 km upstream from the river mouth was not significantly different between wild (20.6 km day^?1) and farmed (19.8 km day^?1) salmon. Wild salmon tagged when water flow in the river was increasing had a significantly higher migration speed than wild salmon tagged when water flow was decreasing. This was not true for farmed salmon. Farmed salmon were distributed significantly higher up the river than wild salmon during spawning, although both types of fish were found together in spawning areas. Thus, there was no geographical isolation to prevent spawning between wild and escaped farmed salmon. Farmed salmon had significantly more and longer up- and downstream movements than wild salmon during the spawning period. Unlike farmed salmon, the number of riverine movements by wild salmon increased significantly when variation in water flow increased. A smaller proportion of wild (9%) than farmed (77%) salmon survived through the winter after spawning.     

A test of the cumulative effect of river weirs on downstream migration success,speed and mortality of Atlantic salmon (Salmo salar) smolts: An empirical study

This study investigated the cumulative impact of weirs on the downstream migration of wild Atlantic salmon (Salmo salar) smolts in the River Foyle, Northern Ireland. In spring of 2013 fish were released in two tributaries of similar length; one tributary (impacted) had seven low‐head weirs along the migration pathway and the other was devoid of such structures (un‐impacted). Salmon smolts fitted with acoustic transmitters were monitored via a passive acoustic telemetry array during downstream migration. In 2014 the study was repeated only in the impacted tributary. Overall freshwater survival rates were high (>94%). There was no significant difference in mortality, movement pattern, delay or travel speeds between rivers or between years at any phase of migration. Escapement of salmon smolts through Lough Foyle (a marine sea lough) to the open ocean was low, approximately 18% in each year. Escapement did not differ between impacted and un‐impacted rivers. This study showed no postpassage effects of weirs on mortality, migration speed or escapement of downstream migrating smolts. This suggests that the elevated mortality at low‐head obstacles described in other studies is not inevitable in all river systems. Migration through rivers with natural riffle‐pool migration may result in similar effects as those from low‐head weirs. Causes of apparent high mortality in the early part of marine migration in this study, are unknown; however similar studies have highlighted the impact of fish predators on smolts.     

An additional life-history tactic of masu salmon: Migration of parr to coastal habitats

Alternative life-history tactics of masu salmon Oncorhynchus masou are well documented. Subsequent to the freshwater parr stage (age ≥ 1 + years), an anadromous form migrates to the sea after smolting, while a resident form matures without seaward migration. In addition to this typical migratory dimorphism, anecdotal reports based on field observations have indicated that some underyearling masu salmon use estuarine waters. However, no empirical evidence indicates saltwater utilisation and subsequent survival in the early parr stage. Here, we used otolith microchemistry to examine whether a portion of masu salmon parr in northern Japan enters coastal habitats. The otolith Sr:Ca ratios of most juveniles collected from six rivers had consistently low values, indicating that masu salmon parr inhabiting these rivers stay only in freshwater. In contrast, in individuals from a steep-gradient river the Sr:Ca ratios increased at about a 200-µm distance from the otolith core. These results suggest that some masu salmon parr might use brackish water or sea water temporarily. In addition, three masu salmon parr were found in another steep river where a culvert located only ten metres from the river mouth completely blocked upstream migration for spawning. The Sr:Ca ratios in these fish increased at about >200 µm from the otolith core, indicating the parr had immigrated to the non-natal river from the sea. Such flexible behaviour at an early life stage may contribute to the spatial expansion of masu salmon, and the movement could moreover help to stabilise its population dynamics.     

Comparative feeding, growth and movements of Atlantic salmon (Salmo salar) parr from riverine and estuarine environments

Abstract– The diet composition, movcments and growth of Atlantic salmon parr rearing in the estuary of Western Arm Brook, Newfoundland were compared with those of parr from riverine habitats over 2 years. Estuarine parr consumed a variety of prey, including many freshwater taxa (mainly insects), which indicated a dependence on freshwater drift from the river. Prey of estuarine origin (amphipods and sticklebacks) were increasingly consumed between spring and autumn. Prey volume per fish and number of prey per fish increased significantly for estuarine parr between spring and autumn, suggesting an improvement in food availability. Riverine parr, however, realized a general decrease in both parameters between spring and autumn. The recapture of 16% ( n = 131) of the 829 parr marked in the estuary in 1987 and 1988 indicated a directed movement toward the head of the estuary and river mouth, as also suggested by the diet analysis. Parr from outer estuary sites were very mobile compared with parr from the estuary site closest to the river mouth, which behaved more like parr in the river proper in displaying strong site fidelity. Movement patterns of parr were primarily along the shoreline. Individual growth rates were highly variable in both environments but especially in the estuary. The mean growth of estuarine parr was 0.23 mm. d⁻¹ between May and October with some evidence of fastest growth having occurred in late spring and early summer (approx. 0.4 mm. d⁻¹); mean growth rate of riverine parr was slower, at 0.12 mm. d⁻¹. The results are discussed in the context that estuarine rearing by salmon parr represents an alternative life-history tactic for the species in river systems in eastern Canada.     

Evidence for spatial coherence in time trends of marine life history traits of Atlantic salmon in the North Atlantic

A hierarchical Bayesian life cycle model is presented that considers spatial covariation of marine life history traits of Atlantic salmon (Salmo salar) populations in the North Atlantic. The model is based on a collective analysis of the dynamics of 13 stock units (SUs) from two continental stock groups (CSGs) in North America and Southern Europe in a single hierarchical model over the period 1971–2014. The model sets up a new assessment framework for Atlantic salmon stocks. It also provides a framework to investigate the drivers of changes in Atlantic salmon population dynamics including disentangling the effects of fisheries from those of environmental factors in a hierarchy of spatial scales. It is used to test the hypothesis of a strong spatial synchrony in marine life history dynamics of Atlantic salmon populations. The trends in two key parameters associated with the early marine phase of the life cycle are estimated: (i) the marine survival during the first summer–autumn spent at sea and (ii) the proportion of fish maturing after the first winter at sea. The results provide evidence of a decline in the marine survival together with an increase in the proportion of fish that mature after the first winter at sea, common to all SUs. Our results show an increased coherence in the covariations of trends in these two marine life history traits related to geographic proximity of SUs which support the hypothesis of a coherent response of geographically proximate Atlantic salmon populations that likely share similar migration routes.     

Osmotic adaptation of Oncorhynchus kisutch walbaum. I. Seasonal variations of gill Na+K+ ATPase activity in coho salmon,O+-age and yearling,reared in fresh water

An eventual improvement in salmonid production in sea water will depend on a fundamental understanding of the natural osmotic behaviour, which demands, in turn, the seaward migration of young salmonids and the development of osmoregulatory processes. Seasonal changes in the gill Na⁺K⁺ ATPase of coho salmon, Oncorhynchus kisutch, were studied between February 1976 and August 1977, on two successive broods, O⁺-age and yearling, of the same origin and reared under natural conditions in a freshwater hatchery off the Brittany coast (France).The gill ATPase changes are of a rhythmical nature. The data show that a seasonal activation of the branchial Na⁺K⁺ ATPase affects one part of the population only. Both age groups, O⁺-age and yearlings, present two peaks of Na⁺K⁺ ATPase activity during the year, in the spring and in the fall, separated by a low activity period in summer and in winter. The peaks of ATPase activity in the fall (both groups) and spring (yearlings) correspond, roughly, with the equinox, whereas the spring rise of O⁺-age fish starts later on.The levels of gill ATPase activity are, probably, a function of the fish size for a given season, and the duration of Na⁺K⁺ ATPase activation may be affected by high temperatures of the late spring and thus may fluctuate from year to year. Yearly variations in branchial Mg²⁺ ATPase were evidenced in both groups; for the moment, these variations are impossible to correlate with the smolting process.Spring and autumn rises in the gill Na⁺K⁺ ATPase of coho salmon, in fresh water, indicate changes in the osmoregulatory physiology, that are preparatory to seaward migration.As a consequence, assays of gill ATPase activity can give aquaculturists some precise indications of the migratory tendencies in young fresh water salmon and thus the euryhalinity possibilities of the species at a given time.     

Importance of the River Teviot to Atlantic salmon, Salmo salar, rod catches in the River Tweed, Scotland

Abstract  The body mass distributions and variations in abundance of the spring and autumn catches of Atlantic salmon, Salmo salar L., were compared between fisheries above and below the confluence of the rivers Tweed and Teviot, Scotland. Significant differences between the distributions were found over three periods, one in spring and two in autumn, when salmon catches were high. Correlations were found between abundance trends for periods when distributions were similar or dissimilar. Abundance of salmon returning to the River Teviot was proportional to the main river. However, its population structure differed when abundances were high, suggesting different survival strategies. It appears that changes in the numbers returning to the river were resultant of changes in the marine rather than freshwater environment.     

Seasonal adjusted diets to Atlantic salmon (Salmo salar): Evaluations of a novel feed based on heat-coagulated fish mince, fed throughout 1 year in sea: Feed utilisation, retention of nutrients and health parameters

The present paper reports the results of a 1 year experiment using Atlantic salmon with a starting weight of 1.7 kg, and final weight of 7.4 to7.8 kg dependent of diet group. The experiment aimed to evaluate a direct production method of feed where landings from fishing vessels are used directly in feed processing. The dietary compositions followed the natural rhythm in lipid level of the catches of herring in the North Sea (Catch group) adjusted to be stable throughout one season only, and compared to a control diet (constant composition throughout the year) and a designed diet (opposite to the natural biorhythm of salmon lipid stores) (diet group Design). Four seasons were defined: spring (March, April, May), summer (June July August), autumn (September, October, November), winter (December, January, February). All diets varied in protein and lipid due to the adjustment according to season. The experiment was run in triplicate sea cages for each diet, using natural light and temperature regimes (21°N). All diet groups showed equal growth throughout each season, except for the Catch group during autumn showing lower SGR-values. SGR values varied significantly also between seasons for all diet groups, ranging from 0.29 during spring to 0.81 during autumn. Feed conversion ratio varied dependent on season and the dietary protein to energy ratio, at all seasons except winter. Quite a large variation between diet groups and seasons were registered in condition factor. Whole body lipid varied between seasons, as a consequence of dietary lipid levels, and increased as fish weight increased. After autumn growth only, whole body protein levels were significantly lower in the Catch group compared to the two other diet groups. Muscle lipid levels did not vary as a consequence of fish size alone, but varied substantially between seasons in both the Catch and Control groups, but not in the Design group. Muscle alpha-tocopherol and fatty acid profile varied due to diet in spring and autumn seasons, but with minor variations due to diet in summer and winter periods. Only minor influences from diet were registered in liver and heart compositions. Haematological parameters and plasma nutrient values ranged within normal values for salmon, and together with close to no mortality throughout the experiment, fish health was concluded to be good in all diet groups at all seasons. However, plasma asparagine aminotransferase (ASAT) values were quite high during summer and autumn, especially in the control group. These results point to the need of optimizing antioxidant composition of diets during the summer and early autumn season. Overall results show the possibility to obtain acceptable production results when feeding Atlantic salmon a diet adjusted to each season, as long as the fish protein to energy (P:E) requirements are met, further that total body lipid stores varied more than muscle lipid concentrations, and that the lipid levels were highly dependent on season, diet composition and fish size.