Determining the mechanisms driving range-wide reductions in Atlantic salmon marine survival is hindered by an insufficient understanding of their oceanic ecology and distribution. We attached 204 pop-up satellite archival tags to post-spawned salmon when they migrated to the ocean from seven European areas and maiden North American salmon captured at sea at West Greenland. Individuals migrated further north and east than previously reported and displayed increased diving activity near oceanographic fronts, emphasizing the importance of these regions as feeding areas. The oceanic distribution differed among individuals and populations, but overlapped more between geographically proximate than distant populations. Dissimilarities in distribution likely contribute to variation in growth and survival within and among populations due to spatio-temporal differences in environmental conditions. Climate-induced changes in oceanographic conditions will alter the location of frontal areas and may have stock-specific effects on Atlantic salmon population dynamics, likely having the largest impacts on southern populations.
Temperatures have increased in the north Atlantic and Pacific oceans over the last few decades, causing large-scale oceanographic changes1,2 and northward distributional shifts of many species3,4. Diadromous Atlantic salmon (Salmo salar) and Pacific salmon (Oncorhynchus spp.) spawn and spend the juvenile phase in rivers and perform long-distance ocean feeding migrations5,6. It has been suggested that many of these species have expanded their marine feeding areas northwards7,8, resulting in longer migration distances to foraging areas.
In Europe and North America, the abundance of Atlantic salmon has generally declined since the 1970s9,10. One of the major hypotheses for the decline is reduced marine survival9,10. This has increased interest in the spatio-temporal ocean distribution of Atlantic salmon11,12 and the impacts of the ocean environment on individual growth and survival13,14. However, the causal links between ocean processes and survival remain elusive. A key element in identifying and evaluating factors that contribute to reduced survival is knowledge of migration routes, migration timing and feeding areas. With knowledge of the oceanic distribution of salmon from different regions, the causative mechanisms underlying the variation in growth and productivity can be better understood.
The Atlantic salmon is one of the world’s most studied fish, but detailed knowledge of its ocean distribution and behaviour is limited. Traditionally, information on the ocean migration originated from sampling and conventional tagging surveys based on mark and recapture methods15,16. More recently, genetic studies have disentangled novel aspects of the species’ ocean migration and distribution17,18,19. These previous studies have been spatially limited by primarily sampling from fisheries and surveys at the Faroes, Greenland and in the Norwegian Sea20 rather than over more widespread regions that Atlantic salmon are believed to use. They have also provided little information on detailed migration routes and behaviour.
The development of electronic tracking technologies has opened new possibilities to collect detailed spatially unbiased information on fish migrations and individual behaviour over large ocean areas21,22. For Atlantic salmon, the use of archival tags has expanded our knowledge of where they feed in the ocean12,23,24,25,26 and provided detailed data on individuals’ depth and temperature use27,28,29. However, archival tags have typically been used in studies of single populations, or in limited geographical areas, and included a low number of individuals.
To increase our understanding of the ocean distribution of Atlantic salmon, and to study variation in distribution between and within populations, we performed a large-scale study using pop-up satellite archival tags (PSATs) spanning populations from the southernmost to the northernmost part of the species’ distribution range. The study included post-spawned salmon from seven areas in Europe (from 42° N in Spain to 70° N in northern Norway) that were tagged as they were leaving the river and returning to the sea, and maiden North American salmon captured at sea at Western Greenland. The tags archived environmental data until detachment when they reported their location and transferred stored data to satellites. Our aims were to (1) map the horizontal ocean migration patterns of individual Atlantic salmon, (2) examine how their migration patterns were related to origin, travel distance, area use and diving frequency, and (3) quantify the overlap in feeding areas of salmon from the different regions.
From the 204 tagged fish, data were obtained from the PSATs of 148 Atlantic salmon, of which 105 provided enough data for estimating complete migration paths while the remainder provided pop-up locations indicating the approximate position of the animals on the date the tag released. The migration tracks calculated for these fish showed that individuals migrated towards known oceanographic fronts, where branches of the North Atlantic current lie adjacent to cold polar waters, but the oceanic distribution differed among individuals and populations (Fig. 1). Most Norwegian and Danish salmon conducted a rapid northern or north-western migration in the North Atlantic Ocean (Fig. 1). However, salmon from northern Norway either migrated north-west in the northern Norwegian Sea toward Svalbard or the Greenland Sea, or north-east to the Barents Sea (Fig. 1). The northernmost recordings of Norwegian and Danish Atlantic salmon were from the west of Svalbard at latitudes of nearly 80° N. In contrast, Irish, Spanish and Icelandic salmon primarily migrated westward towards East Greenland (Fig. 1). Maiden North American salmon (genetically assigned) tagged at Western Greenland migrated south into the Labrador Sea during fall and winter.
Most salmon rapidly migrated towards the oceanographic fronts (Fig. 1). Within each population, individuals commonly migrated in similar directions, although population-specific variation was noted (Fig. 1). Individuals covered distances of up to 2940 km from the release site, measured as a straight-line distance from the tagging site to the pop-up position (an individual from River Lerez in Spain with the longest migration), with fish released further south travelling the longest distances (Table 1; Fig. 1). For the populations with multiple years of tagging (i.e., salmon from 2 years in Denmark and 3 years in Northwest Norway, Table 1), the migration routes showed similar patterns between or among the years (Fig. 2).
Tagged salmon were predominately surface oriented, spending 80% of the time at depths less than 10 m, with occasional dives to greater depths (population-specific maximum depths from 220 to 870 m, Table 1). The frequency of dives to depths greater than 10 m increased for the southernmost populations during their post-migration period (i.e., when they had reached the most distant areas from their home river) (Fig. 3). For the north-Norwegian populations this pattern was less clear, and the salmon initiated frequent diving soon after they had entered the open ocean.
The overlap in the area use during the ocean migration varied substantially among the different populations, with greater overlap in ocean distribution between geographically proximate than distant populations (Fig. 4; Table 2). Populations from Denmark and Norway had the greatest overlap in distribution areas, with the northeast Norwegian population being the exception, with no overlap with Danish populations. Also, the populations from Spain and Ireland had a relatively large overlap in their distribution area. The Spanish and Irish fish did not overlap in distribution with Norwegian fish, and only to a small extent with Danish fish. The North American fish tagged at Greenland only overlapped to a small extent with the Irish fish (Fig. 4; Table 2). Temporal area use is not considered here, and the extent of overlap in area use among populations may be smaller if considering the time of the season different populations spend in different areas.
Thermal experience of fish from the different populations (Fig. 5) reflected the composition of the water masses encountered from the start of their migration and towards or along the polar front areas. Salmon from Denmark and Norway occupied cool northern Atlantic and/or Barents Sea water (daily averages from 0 to 11 °C depending on time of year). In contrast, salmon from the Irish, Spanish and Icelandic populations exploited generally warmer waters (5–16 °C) towards the areas south of Greenland in the western branch of the North Atlantic current. Maiden North American salmon tagged at Greenland occupied cool water (0–7 °C) in the West Greenland current and within the same range as the Norwegian populations during the same autumn and winter months (Fig. 5). The coldest winter temperatures experienced was by the north-western Norwegian population (average around 2 °C during February–April). However, this population and the salmon tagged at West Greenland were the only fish with data from this period.
Our study extends the known geographic area used by salmon during their migration in the North Atlantic Ocean and Barents Sea as reported by earlier studies based on conventional tagging and sampling surveys15,16,20. An extended use of the North Atlantic Ocean and Barents Sea was also suggested in recent studies using archival tags12,23,24,25,26,28, but these studies have concentrated on single populations or been restricted by low sample sizes. The present study indicated that multiple individuals from the Norwegian and Danish populations survived to migrate northward from their home river and reached latitudes as high as 80° N. This is to our knowledge the furthest north any Atlantic salmon has ever been recorded, extending previously assumed northern limits8,30. These results confirm that the foraging areas of Atlantic salmon currently extend to more northerly latitudes than previously thought. For populations in Denmark and Norway, the marine distribution is probably limited by the northern boundary of Atlantic currents. In contrast, the populations from Iceland, Ireland and Spain did not travel as far north, but instead crossed the main North Atlantic current and migrated towards southern Greenland, indicating a difference in ocean distribution for these populations. The less directed migration displayed by most of the North American salmon tagged at Greenland was likely due to these fish already being present at their assumed main ocean feeding grounds at the west coast of Greenland15 when tagged.
Despite the fact that salmon from different areas used different migration routes and ocean areas, they consistently migrated to and aggregated in assumed highly productive areas at the boundaries between large-scale frontal water masses where branches of the North Atlantic current lie adjacent to cold polar waters31. In these areas, previous analyses demonstrated frequent diving activity by tagged individuals28. The duration and diving profile of these dives suggested foraging behaviour, rather than predator escape, because the dives were U-shaped, typically lasted a few hours, and diving depths were related to the depth of the mixed layer during the different seasons28. Thus, the increased diving frequency is most likely an indication of increased feeding activity, emphasizing the importance of these productive regions as feeding areas for Atlantic salmon. In contrast to Atlantic salmon from the other areas, the two northernmost populations displayed a high diving frequency close to the shore immediately after sea entrance, as also shown by Hedger et al.28. These rivers are located closer to the frontal water masses, and these fish may have started extensive feeding earlier in their sea migration. This assumption is further supported by a study of Norwegian post-smolts, where the northernmost populations were feeding more extensively just after leaving their rivers than fish from southern populations32. Thus, the northern populations may benefit from a shorter migration route to the main feeding areas for salmon. However, given that many kelts are in poor condition when they enter the sea, it is likely that tagged fish from all populations were feeding pelagically in the first weeks at sea during the transit away from the coast when prey were available.
Migration from the rivers to the assumed foraging areas (i.e., the most distant areas they migrated to) was fast and direct for individuals from southern populations, while salmon from the northern Norway did not display similar direct migration routes. Our results are similar to those reported by an earlier study26 on the same North-Western Norwegian population as in the present study, and are likely related to the greater proximity to ocean frontal areas and rich food resources.
The results in the present study may have been influenced by the relatively large size of the tag compared to the size of the fish. Hedger et al.33 assessed tagging effects of PSATs on post-spawned Atlantic salmon by comparing their behaviour with salmon tagged with much smaller archival tags. They found that the overall depth distribution, ocean migration routes based on temperature recordings and return rates did not differ between salmon tagged with PSATs and smaller archival tags and concluded that PSATs are suitable for use in researching large-scale migratory behaviour of adult salmon at sea. However, salmon with PSATs dived less frequently and to slightly shallower depths33. Based on this, we believe the conclusions of the present study are valid despite potential tagging effects, but the diving depths and frequencies might be underestimated compared to non-tagged fish.
Diet data from adult salmon in the ocean are limited but show that salmon feed on a variety of prey taxa. Typically, herring (Clupea harengus), sand eels (Ammodytes spp.), capelin (Mallotus villosus) and myctophids dominate as fish prey, while euphausiids and amphipods often dominate as crustacean prey34,35,36. Although there exist some data of adult herring and capelin during parts of the year, there is limited information on the spatial and temporal distribution of crustaceans in these ocean areas, and it is therefore difficult to relate the salmon diving behaviour to availability of all their main prey items. However, salmon appeared to be able to forage on prey far below the surface, indicated by the frequent dives, and salmon at sea have also previously been shown to feed on the mesopelagic community37,38. Hedger et al.28 found that the diving depth increased with the depth of the mixed layer and hypothesised that stratification affected the aggregation of prey and thereby the salmon diving behaviour. They also showed that when the stratification disappeared during the dark winter months, the salmon dived less but their dives were deeper. Nevertheless, the possibilities to feed at different depths28, expand the foraging niche of salmon compared to feeding merely near the surface.
Dadswell et al.11 published the “merry-go-round hypothesis”, which implies that both first-time migrants and previous spawners from all salmon populations enter the North Atlantic Subpolar Gyres and move counter clockwise within these gyres until returning to their natal rivers. Although the full migration from river outrun to return was not followed in the present study (most tags popped off half-way into the migration), and some individuals indicated a counter clockwise migration pattern, most of the populations and individuals in this study clearly did not follow the North Atlantic Subpolar Gyres during the first months at sea. Therefore, most of our data did not support the merry-go-round hypothesis. However, some individuals from northern Norway seemed to follow the currents to a larger extent than individuals from other populations during the first months at sea. Previous studies on Atlantic salmon from Canada also documented that adults migrated either independently or against prevailing currents while at sea, indicating that the horizontal movement of adults are primarily governed by other factors12,24.
Due to the size limit of the pop-up-tags, we primarily tracked large post-spawned individuals that are more mobile than smaller first-time migrants. Although some studies have shown that first-time migrants can be found in the same areas as post-spawners from the same populations8,30 is not known to which extent the migration pattern and distribution of post-spawners represent the same migration pattern of first-time migrants. Due to a larger body size, it is possible that the migration of post-spawners depends to a lesser degree on ocean currents and gyres than do the movements of first-time migrants, especially in the first part of the migration. For example, we observed that the Irish and Spanish post-spawned individuals all crossed the main North Atlantic current towards Greenlandic waters. However, Irish and other southern European post-smolts have frequently been captured in the Norwegian Sea20, indicating that some of these individuals migrate and follow the main ocean current in a northward direction. It is possible that many of these post-smolts later migrate southwest towards Greenland and feed in these waters as maiden salmon before they return to rivers. This corresponds to the observation that it is mostly large (two sea-winter) southern European salmon (including Irish individuals) that are found in the southern Greenland feeding areas20. Therefore, it might be that the post-spawned salmon from these populations return to their primary feeding areas where they were feeding as maiden salmon from their first sea migration, and not necessarily to the same area as they started their feeding migration as post-smolts.
Populations differed in their ocean distribution, but the distribution also overlapped to some degree between or among populations, with more overlap between geographically proximate than distant populations. Some populations never overlapped in geographical distribution during the study. The populations from Ireland and Spain did not overlap with the Norwegian and Danish salmon, but there was a small spatial overlap between the Irish salmon and the North American salmon tagged at Greenland, although area use by these populations did not overlap in time. It is known that populations from North America and Europe largely use different parts of the North Atlantic, with more North American salmon in the western part and more European salmon in the eastern part of the ocean although they have been shown to mix at the feeding grounds at the Faroes and at Greenland12,15,16,18,20. For the Spanish population, it should be noted that tagged individuals were followed for a relatively short period, and a larger sample size over a longer period might have shown some overlap with the northern European populations, based on the initial northward direction of two individuals. At the same time as populations differed in their ocean distribution, there were also relatively large within-population differences in migration routes and geographic distribution. Individual differences in migration routes and ocean distribution of salmon from the same population, even within the same year, were also shown by Strøm et al.12,26. Collectively, these results imply that salmon from different populations will experience highly different ecological conditions, potentially contributing to between-and within-population variation in growth and survival. Since our data are limited by a varying number of individuals among the studied populations, and restricted mainly to post-spawned salmon, our results represent a minimum overlap among the populations so the actual overlap may be larger. Nevertheless, this strongly indicates a varying degree of geographical separation in ocean feeding areas. Thus, geographically close populations will to a larger extent be influenced by similar conditions in the ocean than more distant populations.
The study was carried out over several years, with not all sites having tagging undertaken in the same years. There is a possibility that geographic area use and overlap among populations may vary among years, according to variation in environmental conditions among years29. However, data from multiple years for some populations suggest consistent population specific migration routes and area use among years, indicating that the principal patterns are stable over time for particular salmon populations.
The differing distributions of salmon from particular populations in different oceanic regions might simply be a function of distance to appropriate feeding grounds from the different home rivers, with individuals from the different rivers mainly adapted to seek the closest feeding areas. The route selection during the migration might in addition be a result of each individuals’ opportunistic behaviour and which food resources and environmental conditions they encounter along the journey. As discussed above, the experience and learning during the first ocean migration might also impact individuals’ route choice and area use. Salmon from southern populations used more southern ocean areas, and hence stayed in warmer water, than salmon from the northern populations. We cannot rule out that salmon from different populations have different temperature preferences due to different thermal selection regimes in their home rivers, but similar to a previous study29, we suggest that the differences in thermal habitat among populations utilising different areas at sea are mainly driven by availability of prey fields. There is generally little support for the hypothesis that variation in salmonid growth rates reflects thermal adaptations to their home stream39.
Despite the variation in migration patterns among and within populations, most individuals seemed to migrate to distant ocean frontal areas. This suggests that climate change may have greater impact on populations originating further south, because the distances and time required to travel to feeding areas will increase if the boundary between Atlantic and Arctic waters move northward because of ocean warming. Our study has shown that several populations are able to migrate over large distances, but the capacity for populations to adapt to an increased migration distance is unknown. Given increased migration time, especially for southern populations, the time available for accumulating important energy reserves will likely be reduced. In addition, increased water temperatures in the North Atlantic may also increase the energy expenditure that the individual fish spend per unit of distance when migrating from their home rivers towards the feeding areas. This may affect all populations to some degree, and may contribute to an additional burden for Atlantic salmon populations that are already in a poor state. This will also add to the hypothesized negative effect of climate change in freshwater for the southern populations, where temperatures will have a greater likelihood of reaching to growth inhibiting levels compared to more northern populations39.
Taking advantage of the development of electronic tags, we have shown an extended use of the North Atlantic Ocean by Atlantic salmon, including the Barents Sea, which contrasts to the earlier strong focus on feeding areas at the Faroes, West Greenland and in the Norwegian Sea in previous studies. These results expand the knowledge on the marine foraging and habitat niche of Atlantic salmon, in terms of geography, migration behaviour and thermal niche. The existence of feeding areas at the boundaries between Atlantic and Arctic surface currents suggests that salmon have a strong link to Arctic oceanic frontal systems. We have further shown that salmon from different populations may migrate to different ocean frontal areas in the North Atlantic Ocean and Barents Sea and therefore be impacted by different ecological conditions that may contribute to within-population variation in growth and survival. We also conclude that climate induced changes in oceanographic conditions, which will likely alter the location of and distance to polar frontal feeding areas, may have region-specific influences on the length and cost of the Atlantic feeding migrations, particularly affecting the southern populations most. As the polar oceans get warmer and current patterns shift, changes in the location and productivity of high latitude fronts will become evident. As migration distances become longer, or more variable, and the time accumulating energy is reduced, the variation in the marine survival and productivity of different populations are likely to become more marked. Combined, our results help to shed light on important ecological process that shape Atlantic salmon population dynamics within most of its distribution area.
Material and methods
Capture and handling of Atlantic salmon for tagging
Atlantic salmon post-spawners from seven European areas were tagged with pop-up satellite archival tags (n = 204, Table 1). The sites included north-eastern Norway (River Neiden), north-western Norway (River Alta), Mid Norway (River Orkla), Denmark (River Skjern and Varde), Ireland (Rivers Blackwater, Suir, Nore and Barrow), Spain (River Lérez) and Iceland (River Laxa). In addition, maiden salmon captured and tagged at Greenland (Nuuk) were included to provide information on Atlantic salmon in the north-western Atlantic Ocean. The Greenland fish were all of North American origin, as confirmed by genetic analyses40. Salmon post spawners were caught in rivers during spring by electrofishing (Denmark), in a trap (Spain) or by angling (Norway, Ireland and Iceland) and placed in a net pen in saltwater (about 5 × 5 × 5 m) (Norway, Ireland) or in a freshwater tank close to the river mouth for 1–2 weeks (Denmark and Iceland). The Spanish salmon were kept in a circular freshwater tank (3 m in diameter, 1.5 m deep) for up to 3 months before tagging.
The largest individuals were selected for tagging due to the size of the tags. The maiden salmon at Greenland were captured in constantly tended gillnets (n = 19), trap nets (n = 4) or rod (n = 1). Upon capture, fish were transferred to a 400 l water tank on board a boat, where they were tagged and released post-recovery close to the capture location.
Tags, tagging and release
The pop-up satellite archival tags (PSAT model X-tag, size 120 × 32 mm plus 185 mm long antenna, 40 g in air, Microwave Telemetry Inc. Columbia, Maryland, USA) were slightly buoyant and programmed to release from the fish on a certain date or when the fish had remained at a constant depth for 4 or 5 days (in the case of fish mortality, or the tag attachment was expelled from the fish). Once at the surface, the tag location was received by ARGOS-satellites, and the tag transmitted a subset of archived data (depth, temperature and estimates of sunset/sunrise times) to the satellites (http://www.argos-system.org), with a temporal resolution of 15–60 min depending on the deployment duration.
Before tagging, the fish were anaesthetised by using MS-222 (Ireland, Iceland and Greenland), benzocaine (Denmark and Spain), or 2-phenoxyethanol (Norway) and brought to a tagging cradle where body length and mass were measured. The tags were attached externally to individual fish by bridling the tag to two cushioned back plates that were wired through the dorsal musculature below the dorsal fin28. The tag mass averaged 0.57% of the fish body mass (range 0.40–0.74%). A numbered custom-made disc tag (http://www.floytag.com) with contact information was attached to one of the plates in case the fish was recaptured to test for tagging effects in a separate study33.
After tagging, the fish were placed in a large tank or cage and released as soon as they appeared recovered, e.g., breathing and swimming normally and reacting when tactile pressure was applied to the tail base. Since the tags would release if they were at constant depth for 4–5 days we did not want the salmon to remain in the rivers with homogeneous depth after tagging. Therefore river-captured salmon were transported 5–15 km away from the river mouth before release.
The experimental procedures were in each case approved by national authorities. All methods were carried out in accordance with relevant guidelines and regulations and fish tagging was approved by the Norwegian Animal Research Authority, the Animal Experimentation Council of Denmark (incl. Greenland), The Icelandic Animal Research Authority, the Department of Health and Children Ireland, and the Ponteverda Province Spain.
Data recovery and analysis, reconstruction of ocean migration
In total, data from 148 Atlantic salmon from a total of ~ 15,000 days were recovered (Table 1). Average data recovery from the PSATs was 69% of the data that could potentially have been recovered. Migration tracks from release of the fish after tagging until the tag popped up could be estimated for 105 salmon based on daily geographic location estimates (Fig. 1). The pop-up location of the tag was provided for 43 additional salmon (Fig. 1).
Geolocation of tagged fish to reconstruct oceanic migration was done using hidden Markov models (HMMs). HMMs are state space models that generate a series of non-parametric spatial probability distributions by a forward–backward recursion on a defined spatial grid41. HMMs enable geolocation of animals in scenarios when light-based geolocation estimates are either poor or absent41.
The HMM developed by Pedersen41 was the primary model used for geolocation. The results were compared to outputs generated by using the method described by Strøm et al.12 to quantify potential biases in estimated migration route caused by the structure of the geolocation models. In both models, daily data likelihoods were calculated using the estimated location (latitude and longitude), mean daily temperature at the surface (< 20 m) and maximum depth12,41. The only major difference between the two models was the spatial grid defining the model domain, resulting in some structural difference in the underlying random walks. In the approach developed by Pedersen41 the spatial grid was discretised based on latitude and longitude, whereas in the method used by Strøm et al.12, the grid was discretised based on distances. In both models, individual migration routes were reconstructed using the mean of 1000 random tracks42. The comparison of outputs between the two models showed little differences between individual migration trajectories, indicating that the outputs were not affected by the spatial structure of the models.
Population-specific ocean distributions were quantified by calculating the combined residency distributions (RDs) for all fish with ocean migrations exceeding 10 days. RDs are the cumulative probability distribution for the entire spatial domain and provide an estimate of the ocean distribution that includes the uncertainty of the data41. The spatial overlaps among populations were determined by calculating the overlap in population-specific RDs using Bhattacharrya’s affinity43. Icelandic data were too few to be included. Data from the two Danish populations were combined in temporal and annual comparisons, because they belong to rivers close to each other. Depth data for salmon from Rivers Alta, Neiden and Orkla in Norway have previously been analysed in relation to day length and temperature stratification by Hedger et al.28, but not in relation to their modelled migration routes as in the present study.
Data will be made available upon request.
Hoegh-Guldberg, O. & Bruno, J. F. The impact of climate change on the world’s marine ecosystems. Science 328, 1523–1528 (2010).
Straneo, F. & Heimbach, P. North Atlantic warming and the retreat of Greenland’s outlet glaciers. Nature 504, 36–43 (2013).
Cheung, W. W. L., Brodeur, R. D., Okey, T. A. & Pauly, D. Projecting future changes in distributions of pelagic fish species of Northeast Pacific shelf seas. Prog. Oceanogr. 130, 19–31 (2015).
Fossheim, M. et al. Recent warming leads to a rapid borealization of fish communities in the Arctic. Nat. Clim. Change 5, 673–677 (2015).
Thorstad, E. B., Whoriskey, F., Rikardsen, A. H. & Aarestrup, K. Aquatic nomads: The life and migrations of the Atlantic salmon. In Atlantic Salmon Ecology (eds Aas, Ø. et al.) 1–32 (Blackwell Publishing Professional, 2011).
The Ocean Ecology of Pacific Salmon and Trout (American Fisheries Society, 2018).
Nielsen, J. L., Ruggerone, G. T. & Zimmerman, C. E. Adaptive strategies and life history characteristics in a warming climate: Salmon in the Arctic?. Environ. Biol. Fishes 96, 1187–1226 (2013).
Jensen, A. J. et al. Origin and life history of Atlantic salmon (Salmo salar) near their northernmost oceanic limit. Can. J. Fish. Aquat. Sci. 71, 1740–1746 (2014).
Chaput, G. Overview of the status of Atlantic salmon (Salmo salar) in the North Atlantic and trends in marine mortality. ICES J. Mar. Sci. 69, 1538–1548 (2012).
ICES. Report of the Working Group on North Atlantic Salmon (WGNAS). ICES Scientific Reports (2020).
Dadswell, M. J., Spares, A. D., Reader, J. M. & Stokesbury, M. J. W. The North Atlantic subpolar gyre and the marine migration of Atlantic salmon Salmo salar: The ‘Merry-Go-Round’ hypothesis. J. Fish Biol. 77, 435–467 (2010).
Strøm, J. F. et al. Ocean migration of pop-up satellite archival tagged Atlantic salmon from the Miramichi River in Canada. ICES J. Mar. Sci. 74, 1356–1370 (2017).
Todd, C. D. et al. Detrimental effects of recent ocean surface warming on growth condition of Atlantic salmon. Glob. Change Biol. 14, 958–970 (2008).
Mills, K. E., Pershing, A. J., Sheehan, T. F. & Mountain, D. Climate and ecosystem linkages explain widespread declines in North American Atlantic salmon populations. Glob. Change Biol. 19, 3046–3061 (2013).
Reddin, D. G. et al. Distribution and biological characteristics of Atlantic salmon (Salmo salar) at Greenland based on the analysis of historical tag recoveries. ICES J. Mar. Sci. 69, 1589–1597 (2012).
Jacobsen, J. A. et al. Distribution by origin and sea age of Atlantic salmon (Salmo salar) in the sea around the Faroe Islands based on analysis of historical tag recoveries. ICES J. Mar. Sci. 69, 1598–1608 (2012).
Bradbury, I. R. et al. Genetic mixed-stock analysis disentangles spatial and temporal variation in composition of the West Greenland Atlantic Salmon fishery. ICES J. Mar. Sci. 73, 2311–2321 (2016).
Gilbey, J. et al. Genetic stock identification of Atlantic salmon caught in the Faroese fishery. Fish. Res. 187, 110–119 (2017).
Bradbury, I. R. et al. Range-wide genetic assignment confirms long-distance oceanic migration in Atlantic salmon over half a century. ICES J. Mar. Sci. https://doi.org/10.1093/icesjms/fsaa152 (2021).
Ó Maoiléidigh, N. et al. Fifty years of marine tag recoveries from Atlantic salmon. ICES Cooperative Research Report No. 343 (2018). https://doi.org/10.17895/ices.pub.4542.
Block, B. A. et al. Electronic tagging and population structure of Atlantic bluefin tuna. Nature 434, 1121–1127 (2005).
Righton, D. et al. Empirical observations of the spawning migration of European eels: The long and dangerous road to the Sargasso Sea. Sci. Adv. 2, e1501694 (2016).
Chittenden, C. M., Fauchald, P. & Rikardsen, A. H. Important open-ocean areas for northern Atlantic salmon (Salmo salar)—As estimated using a simple ambient-temperature approach. Can. J. Fish. Aquat. Sci. 70, 101–104 (2013).
Lacroix, G. L. Population-specific ranges of oceanic migration for adult Atlantic salmon (Salmo salar) documented using pop-up satellite archival tags. Can. J. Fish. Aquat. Sci. 70, 1011–1030 (2013).
Guðjónsson, S., Einarsson, S. M., Jónsson, I. R. & Guðbrandsson, J. Marine feeding areas and vertical movements of Atlantic salmon (Salmo salar) as inferred from recoveries of data storage tags. Can. J. Fish. Aquat. Sci. 72, 1087–1098 (2015).
Strøm, J. F., Thorstad, E. B., Hedger, R. D. & Rikardsen, A. H. Revealing the full ocean migration of individual Atlantic salmon. Anim. Biotelemetry 6, 2 (2018).
Reddin, D. G., Downton, P., Fleming, I. A., Hansen, L. P. & Mahon, A. Behavioural ecology at sea of Atlantic salmon (Salmo salar L.) kelts from a Newfoundland (Canada) river. Fish. Oceanogr. 20, 174–191 (2011).
Hedger, R. D. et al. Diving behaviour of Atlantic salmon at sea: Effects of light regimes and temperature stratification. Mar. Ecol. Prog. Ser. 574, 127–140 (2017).
Strøm, J. F., Thorstad, E. B. & Rikardsen, A. H. Thermal habitat of adult Atlantic salmon Salmo salar in a warming ocean. J. Fish Biol. 96, 327–336 (2020).
Rikardsen, A. H., Hansen, L. P., Jensen, A. J., Vollen, T. & Finstad, B. Do Norwegian Atlantic salmon feed in the northern Barents Sea? Tag recoveries from 70 to 78°N. J. Fish Biol. 72, 1792–1798 (2008).
Raj, R. P., Chatterjee, S., Bertino, L., Turiel, A. & Portabella, M. The Arctic Front and its variability in the Norwegian Sea. Ocean Sci. 15, 1729–1744 (2019).
Rikardsen, A. H. et al. Geographical differences in marine feeding of Atlantic salmon post-smolts in Norwegian fjords. J. Fish Biol. 64, 1655–1679 (2004).
Hedger, R. D., Rikardsen, A. H. & Thorstad, E. B. Pop-up satellite archival tag effects on the diving behaviour, growth and survival of adult Atlantic salmon Salmo salar at sea. J. Fish Biol. 90, 294–310 (2017).
Rikardsen, A. H. & Dempson, J. B. Dietery life-support: The food and feeding of Atlantic salmon at sea. In Atlantic Salmon Ecology (eds Aas, Ø. et al.) 115–143 (Blackwell Publishing Professional, 2011).
Renkawitz, M. D., Sheehan, T. F., Dixon, H. J. & Nygaard, R. Changing trophic structure and energy dynamics in the Northwest Atlantic: Implications for Atlantic salmon feeding at West Greenland. Mar. Ecol. Prog. Ser. 538, 197–211 (2015).
Kelly, B., Benoît, H. P., Chaput, G., Jones, R. A. & Power, M. Spawning-strategy-dependent diets in two North American populations of Atlantic salmon Salmo salar. J. Fish Biol. 94, 40–52 (2019).
Lear, W. H. Food and feeding of Atlantic salmon in coastal areas and over oceanic depths. Res. Bull. (Int. Comm. Northwest Atl. Fish.) 9, 27–39 (1972).
Hansen, L. P. & Pethon, P. The food of Atlantic salmon, Salmo salar L., caught by long-line in northern Norwegian waters. J. Fish Biol. 26, 1087–1098 (1985).
Jonsson, B. & Jonsson, N. A review of the likely effects of climate change on anadromous Atlantic salmon Salmo salar and brown trout Salmo trutta, with particular reference to water temperature and flow. J. Fish Biol. 75, 2381–2447 (2009).
Renkawitz, M., Sheehan, T. F., Rikardsen, A., Righton, D. & Nygaard, R. Tracking Atlantic salmon in the Labrador Sea with PSATs. NEFSC Ref Doc. http://www.nefsc.noaa.gov/publications/(in press).
Pedersen, M. W. Hidden Markov modelling of movement data from fish. Ph.D. thesis. Technical University of Denmark, Kongens Lyngby (2010).
Thygesen, U. H., Pedersen, M. W. & Madsen, H. Geolocating fish using hidden Markov models and data storage tags. In Tagging and Tracking of Marine Animals with Electronic Devices Vol. 9 (eds Nielsen, J. L. et al.) 277–293 (Springer, 2009).
Fieberg, J. & Kochanny, C. O. Quantifying home-range overlap: The importance of the utilization distribution. J. Wildl. Manag. 69, 1346–1359 (2005).
IOC, IHO and BODC. "Centenary Edition of the GEBCO Digital Atlas", published on CD-ROM on behalf of the Intergovernmental Oceanographic Commission and the International Hydrographic Organization as part of the General Bathymetric Chart of the Oceans; British Oceanographic Data Centre, Liverpool (2003).
We thank the Research Council of Norway (project 221400/E40 Salmotrack and 280308 SeaSalar), Tromsø Research Foundation (supported by Trond Mohn), Alta Laksefiskeri Interessentskap, UiT-The Arctic University of Norway (PhD-positions), Atlantic Salmon Conservation Foundation, Danish Rod and Net License Fund, Denmark’s Center for Wild Salmon, Inland Fisheries Ireland, NOAA Fisheries Service (USA), Greenland Institute of Natural Resources and Xunta de Galicia and the Icelandic Salmonid Enhancement Fund for supporting and funding this project. DR was provided with learning and development support from Cefas to contribute to the writing of this manuscript. We also thank all staff, students, and local volunteers who have contributed to the fieldwork. The publication charges for this article have been funded by a grant from the publication fund of UiT The Arctic University of Norway.
The authors declare no competing interests.
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Rikardsen, A.H., Righton, D., Strøm, J.F. et al. Redefining the oceanic distribution of Atlantic salmon. Sci Rep 11, 12266 (2021). https://doi.org/10.1038/s41598-021-91137-y
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