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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.

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An in situ camera set-up was used to study the spawning activity of Atlantic salmon Salmo salar and brown trout Salmo trutta throughout two consecutive seasons in a spawning area affected by hydropower-related pulse flows due to hydropeaking. The purpose was to test whether the flow variation discouraged spawning in shallow areas or motivated spawning into areas with elevated risk of incubation mortality. There were more S. salar observed on the spawning ground during days with high discharge. The presence of S. salar in the spawning grounds was not affected by the hydropeaking cycles of the preceding night. Female S. salar were observed preparing nests within the first hour after water discharge had increased to levels suitable for spawning. In contrast, the number of S. trutta was not correlated with flow and nest preparation was also observed at a discharge corresponding to the lowest discharge levels during a hydropeaking cycle. Survival was generally high in nests excavated the following winter, with only 5·4% suffering mortality due to dewatering. The results suggest that S. salar may respond rapidly to variable-flow conditions and utilize short windows with suitable flows for spawning. Smaller S. trutta may utilize low-flow conditions to spawn in areas that are not habitable by larger S. salar during low flow.

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It was hypothesized that the survival and growth strategies of herring Clupea harengus, displaying a flexible reproductive activity, are adapted to coping with longer periods of prey deprivation (i.e. more variable prey availability), in contrast to cod Gadus morhua, which are adapted to match growth and survival at high prey concentrations. Experimental larval growth and survival data for the two naturally co-occurring species reared either in separate tanks or in combination are presented to test this hypothesis. Natural zooplankton was supplied either ad libitum or in a periodically restricted manner to mimic natural suboptimal conditions. Periodically restricted feeding significantly reduced initial growth of G. morhua larvae co-reared with C. harengus, while no such initial effect was seen for co-reared C. harengus. Overall survival of G. morhua was higher when reared together with C. harengus (32 v. 24%), while C. harengus had higher survival without the presence of G. morhua (59 v. 44%), indicating that both species were affected by higher densities of G. morhua larvae. Furthermore, the final survival in G. morhua was inversely related to average final size, while in C. harengus an opposite trend was observed. How potential behavioural interactions may drive the present results are discussed and contended that a better insight into field vital rates may be gained from further exploration of co-rearing experiments.

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The effects of turbidity, size and the presence of conspecifics on the functional response, feeding latency and activity in the three-spined stickleback Gasterosteus aculeatus were examined. A significant interaction between standard length and presence of conspecifics demonstrated an increase in attack rates of larger individuals in the presence of conspecifics. Attack rate was also higher in turbid water. Feeding latency decreased with prey concentration and presence of conspecifics, but was not affected by turbidity. Activity level did not change with prey levels, but increased with turbidity. These results can help to better understand how individual flexibility in the functional response can affect prey mortality according to environmental perturbation and social interaction at the level of the predator.

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The ability to forage at low light intensities can be of great importance for the survival of fish larvae in a pelagic environment. Three-dimensional silhouette imaging was used to observe larval cod foraging and swimming behaviour at three light intensities (dusk ~1.36 × 10-3 W/m2, night ~1.38 × 10-4 W/m2 and darkness ~3.67 × 10-6 W/m2) at 4 different ages from 6 to 53 days post-hatch (dph). At 6 dph, active pursuit of prey was only observed under dusk conditions. Attacks, and frequent orientations, were observed from 26 dph under night conditions. This was consistent with swimming behaviour which suggested that turn angles were the same under dusk and night conditions, but lower in darkness. Cod at 53 dph attacked prey in darkness and turn angles were not different from those under other light conditions. This suggests that larvae are still able to feed at light intensities of 3.67 × 10-6 W/m2. We conclude that larval cod can maintain foraging behaviour under light intensities that correspond to night-time at depths at which they are observed in the field, at least if they encounter high-density patches of prey such as those that they would encounter at thin layers or fronts.