Jan Grimsrud Davidsen

Genetic versus Rearing-Environment Effects on Phenotype: Hatchery and Natural Rearing Effects on Hatchery- and Wild-Born Coho Salmon

With the current trends in climate and fisheries, well-designed mitigative strategies for conserving fish stocks may become increasingly necessary. The poor post-release survival of hatchery-reared Pacific salmon indicates that salmon enhancement programs require assessment. The objective of this study was to determine the relative roles that genotype and rearing environment play in the phenotypic expression of young salmon, including their survival, growth, physiology, swimming endurance, predator avoidance and migratory behaviour. Wild- and hatchery-born coho salmon adults (Oncorhynchus kisutch) returning to the Chehalis River in British Columbia, Canada, were crossed to create pure hatchery, pure wild, and hybrid offspring. A proportion of the progeny from each cross was reared in a traditional hatchery environment, whereas the remaining fry were reared naturally in a contained side channel. The resulting phenotypic differences between replicates, between rearing environments, and between cross types were compared. While there were few phenotypic differences noted between genetic groups reared in the same habitat, rearing environment played a significant role in smolt size, survival, swimming endurance, predator avoidance and migratory behaviour. The lack of any observed genetic differences between wild- and hatchery-born salmon may be due to the long-term mixing of these genotypes from hatchery introgression into wild populations, or conversely, due to strong selection in nature—capable of maintaining highly fit genotypes whether or not fish have experienced part of their life history under cultured conditions.

Survival, Migration Speed and Swimming Depth of Atlantic Salmon Kelts During Sea Entry and Fjord Migration

In contrast to most species of Pacific salmon (Oncorhynchus spp.), Atlantic salmon (Salmo salar L.) is an iteroparous species such that it may survive and return to spawn repeatedly. Little information exists on these survivors (kelts) even though they might contribute significantly to salmon production when returning as repeat spawners. In order to estimate survival, timing of migration, swimming progression and swimming depth of Atlantic salmon kelts during sea entry and fjord migration, 60 individuals were captured, tagged with acoustic transmitters (of which 20 with depth sensors) and released in the River Alta, Northern Norway. In addition, 172 kelts were also tagged with external Carlin tags to obtain reliable recapture rates in the fisheries. Nearly all (95%) kelts tagged with acoustic transmitters were recorded during their outward migration at four transects of acoustic receivers deployed across the river mouth and Alta Fjord. Most of the kelts migrated through the 30 km long fjord in only 1–2 days (mean time 33 h, range 7–138 h) and generally stayed close to the surface during the fjord migration (individual mean depth of 2 m, range of individual means 0–15 m). Ninety-two percent (55/60) were recorded at the outermost transect 30 km from the river mouth, indicating a high minimum survival rate. The high survival rate and fast progression of kelts throughout the fjord indicate that sea-entry and early sea migration is not a critical phase for Atlantic salmon kelts, despite their weakened condition after spawning and overwintering in the river. Even though kelt migration overlapped partly with the fishing season both in the river and the fjord, and the kelts migrated in shallow waters exposed to several types of fishing gear, reported recapture rates were small (3%, 6 of all 232 tagged kelts).

Early marine migration of European silver eel (Anguilla anguilla) in Northern Norway

To study the migratory behaviour in wild northern European silver eel Anguilla anguilla during sea entry and early marine migration, 32 individuals were tagged with acoustic transmitters and registered at four automatic listening station arrays from the mouth of the north Norwegian River Alta and throughout the Alta Fjord. The A. anguilla entered the fjord during all parts of the tidal cycle and did not seem to utilize the outgoing tidal currents. They migrated mainly during the night, in both the river mouth and the fjord. On average, they spent 2·7 days travelling from the river mouth to the outermost array, 31 km from the river mouth, corresponding to an average migratory speed of 0·5 km h(-1) . The A. anguilla generally migrated in the central part of the fjord and in the uppermost 10-25% of the water column, but with frequent dives to greater depths. Already 4 km after sea entry, A. anguilla were observed diving deeper than 130 m within 20-30 min periods. Hence, this study demonstrated that A. anguilla may perform an active diving behaviour during the early marine migration. The study took place in a pristine area with a minimum of anthropogenic interventions and by individuals from a population still uninfected by the introduced parasite Anguillicoloides crassus. The results may therefore be used as a baseline for future studies of the A. anguilla early marine migration.

Does river of origin influence the early marine migratory performance of Salmo salar

The early marine migratory behaviour of two populations of hatchery-reared Atlantic salmon Salmo salar was compared in a common-garden experiment. Post-smolts from a river in a long fjord (Laerdal River, 144 km from the open coastline, n = 79) and a short fjord (Flekke River, 20 km from the open coastline, n = 80) in western Norway were tagged with acoustic transmitters and released during the spring of 2005 and 2006 in the inner part of the Hardangerfjord system (Opo River mouth, 179 km from the open coastline). The migratory behaviour of the tagged fish was monitored by acoustic listening stations in the fjord system up to 167 km from the release site. The Laerdal fish began migrating before the Flekke fish and had higher progression rates in the middle part of the fjord system. A greater number of Laerdal fish was detected along the most direct migratory route and in the outermost part of the Hardangerfjord system, which is indicative of a higher survival. The results from this study demonstrate differences in early marine migratory behaviour between S. salar from two different stocks and suggest that the distance a S. salar population travels to reach the open coastline may influence its early marine migratory behaviour and performance. The selective pressures of marine predation and arrival time at feeding areas in the ocean may be stronger for stocks with a longer inshore migration, creating more efficient migrants over time.

Does reduced feeding prior to release improve the marine migration of hatchery brown trout Salmo trutta smolts

The aim of this study was to test the hypothesis that hatchery brown trout Salmo trutta smolts, with 50% reduced or no feeding over the last 5 months before release, were more likely to migrate to the sea than individuals with standard feeding ratios. The juvenile fish were divided into three groups 176 days before release: (A) with no feeding, (B) with 50% and (C) with 100% feeding. To study their seaward migration, 40 fish from each feeding group were tagged with acoustic transmitters and tracked by automatic listening stations in the River Nidelva, Trondheim, Norway, its estuary and in the nearest marine environment. At the time of release, mean condition factor was significantly lower in group A and the fish from groups A and B had higher levels of Na+, K+-ATPase. Significantly more fish from group A migrated to the sea, but the rate of downstream progression from release to the estuary did not differ between the three groups. In conclusion, the S. trutta smolts with no access to food in the last 176 day before release were more likely to migrate to the sea. Fish from all three feeding groups, however, appeared to smoltify and had the same rate of downstream progression to the estuary. This indicates that differences in migratory behaviour between individuals from the three feeding groups begin from the time when the fish reach saline waters. It is suggested that feeding in hatcheries has to be greatly reduced (by 50% or more) over several months to have a pronounced effect on the migratory behaviour in S. trutta.

Riverine and near coastal migration performance of hatchery brown trout Salmo trutta

To study migration performance and return rates of hatchery brown trout Salmo trutta smolts the first 5 months after release, 50 fish in each year (fork length, LF , 158-288 mm) were in two subsequent years tagged with acoustic transmitters and recorded by automatic listening stations in the River Nidelva (central Norway), its estuary and in the marine environment. More than half of the smolts became anadromous migrants (52% in 2011 and 70% in 2012). The fish spent longer time in the estuary than in the marine environment and the results suggest that migratory behaviour of S. trutta smolts is not only restricted to be resident or anadrome-lacustrine, but that there is also an intermediary strategy of estuarine feeding. There were no differences in LF or mass between groups of smolts with different migration patterns. Return rates from the sea within the first 5 months after release were in both years 16%. Median progression rate in the river was 0·090 LF s(-1) but decreased significantly as the smolts entered the estuary (0·015 LF s(-1) ). The long residential time in the estuary may increase the risk of negative effects of anthropogenic activities in estuaries, such as harbours and industrial development, and special attention should be given to evaluate effects of such activities.

Interaction between migration behaviour and estuarine mortality in cultivated Atlantic salmon Salmo salar smolts

Migration behaviour and estuarine mortality of cultivated Atlantic salmon Salmo salar smolts in a 16 km long estuary were studied using two methods: (1) acoustic telemetry and (2) group tagging in combination with trap nets. Progression rates of surviving individuals through the estuary were relatively slow using both methods [0·38 LT (total length) s-1 v. 0·25 LT  s-1 ]. In 2012, the progression rate was slow from the river to the estuary (0·55 LT  s-1 ) and the first part of the estuary (0·31 LT  s-1 ), but increased thereafter (1·45-2·21 LT  s-1 ). In 2013, the progression rate was fast from the river to the estuary (4·31 LT  s-1 ) but was slower thereafter (0·18-0·91 LT  s-1 ). Survival to the fjord was higher in 2012 (47%) compared to 2013 (6%). Fast moving individuals were more likely to migrate successfully through the estuary compared to slower moving individuals. Adult recapture of coded-wire-tagged S. salar was generally low (0·00-0·04%). Mortality hot spots were related to topographically distinct areas such as the river outlet (in 2012) or the sill separating the estuary and the fjord (in 2013). At the sill, an aggregation of cod Gadus morhua predating on cultivated smolts was identified. The results indicate that slow progression rates through the estuary decreases the likelihood of smolts being detected outside the estuary. The highly stochastic and site-specific mortality patterns observed in this study highlight the complexity in extrapolating mortality patterns of single release groups to the entire smolt run of wild S. salar.

Marine depth use of sea trout Salmo trutta in fjord areas of central Norway

The vertical behaviour of 44 veteran sea trout Salmo trutta (275-580 mm) in different marine fjord habitats (estuary, pelagic, near shore with and without steep cliffs) was documented during May-February by acoustic telemetry. The swimming depth of S. trutta was influenced by habitat, time of day (day v. night), season, seawater temperature and the body length at the time of tagging. Mean swimming depth during May-September was 1·7 m (individual means ranged from 0·4 to 6·4 m). Hence, S. trutta were generally surface oriented, but performed dives down to 24 m. Mean swimming depth in May-September was deeper in the near-shore habitats with or without steep cliffs (2·0 m and 2·5 m, respectively) than in the pelagic areas (1·2 m). May-September mean swimming depth in all habitats was slightly deeper during day (1·9 m) than at night (1·2 m), confirming that S. trutta conducted small-scale diel vertical movements. During summer, S. trutta residing in near-shore habitat progressively moved deeper over the period May (mean 1·1 m) to August (mean 4·0 m) and then reoccupied shallower areas (mean 2·3 m) during September. In winter (November and February), individuals residing in the innermost part of the fjords were found at similar average depths as they occupied during the summer (mean 1·3 m). The swimming depths of S. trutta coincide with the previously known surface orientation of salmon lice Lepeophtheirus salmonis. Combined with previous studies on horizontal use of S. trutta, this study illustrates how S. trutta utilize marine water bodies commonly influenced by anthropogenic factors such as aquaculture, harbours and marine constructions, marine renewable energy production or other human activity. This suggests that the marine behaviour of S. trutta and its susceptibility to coastal anthropogenic factors should be considered in marine planning processes.

Trophic niche similarity among sea trout Salmo trutta in Central Norway investigated using different time-integrated trophic tracers

From 2011 to 2013, anadromous brown trout Salmo trutta (213−730 mm, total body length, LT) were collected during or shortly after their marine feeding migration at 7 different localities in central Norway. The mean volume of stomach content (%) of marine fish prey eaten by S. trutta captured in marine waters varied from 34 to 89%. There was a high prevalence (67−100%) for parasite groups potentially transmitted by marine prey fish (i.e. nematodes, cestodes and trematodes) at all sampling sites. There was a significant overlap in the signatures of both δ13C and δ15N in the muscle tissue between the 7 groups of S. trutta; however, individual variation within groups was large. A strong positive relationship between δ13C and LT indicated sizedependent niche selection, with smaller individuals feeding less on marine prey and more on brackish or freshwater invertebrates in the estuary. Short-term gut contents data and trophically transmitted parasites showed that all size groups were feeding on marine fish. However, an increased dependence upon marine prey fish by larger S. trutta was indicated by a strong positive relationship between LT and δ15N. Similarities in S. trutta feeding and time-integrated trophic tracers (stable isotopes and parasites) across the 7 localities supports the general view that S. trutta feed within similar marine trophic niches. This similarity in feeding niche requirements may make S. trutta populations vulnerable to anthropogenic ecosystem perturbations which reduce the diversity of potential marine prey items.

Bridging the gap between fisheries science and society: exploring fisheries science as a social activity

Original Article Bridging the gap between fisheries science and society: exploring fisheries science as a social activity Jennifer L. Bailey,* Yajie Liu, and Jan Grimsrud Davidsen Department of Sociology and Political Science, Norwegian University of Science and Technology, Trondheim, Norway Department of Economics, Norwegian University of Science and Technology, Trondheim, Norway Department of Natural History, NTNU University Museum, Trondheim, Norway *Corresponding author: tel: þ47 73598152; fax: +47 73591564; e-mail: jennifer.bailey@svt.ntnu.no