Aslak Darre Sjursen

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.

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.