Home range of juvenile Atlantic salmon, Salmo salar, and brown trout, Salmo trutta, in a Norwegian stream

SUMMARY. 1. The sizes of home ranges of juvenile Atlantic salmon (age 1 +) and brown trout (age 2+ to 9+) in a Norwegian coastal stream were estimated by local movements of batch-marked fish from 12.5 and 25 m long sections. Only recoveries made in the release section and in up-and downstream neighbouring sections were considered.
2. There was no significant difference in the average percentage of recaptures of salmon and trout between 12.5 and 25 m sections; a stream area of about 40–50 m² defines the size of home range for stocks of both species.
3. The fraction of brown trout recaptured in release sections increased with increasing fish densities, indicating a smaller home range under these conditions.     

Partial migration in a landlocked brown trout population

Population densities of landlocked lake‐migratory brown trout Salmo trutta were estimated in two distinct lotic sections, separated by a lentic segment, in the Greåna River, Sweden, and individual growth and habitat use were monitored for 835 tagged brown trout from September 1998 to June 2000. Residency dominated in the upstream section where density of 0+ and 1+ year brown trout was low and growth rate high. In contrast, >90% of the brown trout that migrated to the lake originated from the downstream section, where density was high and growth rate low. For ≥2+ year individuals, growth rate was similar between the two stream sections, but densities were higher in the upstream than in the downstream section. Lake‐migrants had higher growth rates than non‐migrants (residents) during the autumn of both years. From September to May, migrants increased their body mass by >35%, whereas non‐migrants increased by <5%. Approximately 70% of the brown trout moved <10 m and <2% moved between the two stream sections, indicating that the lentic habitat might function as a barrier for juveniles. Differences in migratory behaviour, density and growth between the upstream and the downstream section might indicate that environmental factors influence the decision to migrate. It cannot be excluded, however, that the observed differences are genetically programmed, selected by migration costs that favour migratory behaviour downstream and residency upstream.     

Downstream displacement of post‐emergent brown trout: effects of development stage and water velocity

Brown trout Salmo trutta were introduced at hatching into distinct sections of two parallel artificial channels, one with a constant low velocity (control) and one with velocity changes (experimental), at such times as to produce 12, 3 and 0 day old fish (age after emergences) when the velocity was changed in the experimental channel. This experimental design was repeated in 2002 and 2003 at comparable dates. Young brown trout were sensitive to an increased water velocity for 5 to 6 days after emergence. Water velocity modified the displacement patterns qualitatively but not quantitatively. Eighty per cent of fish moved downstream at all water velocities. Velocity changes, however, advanced the time by which 80% of the fish had displaced downstream.     

Influence of water depth on dispersion of juvenile salmonids, Salmo salar L. and S. trutta L., in a Scottish stream

The dispersion of salmon and trout of 0 +, 1 + and 2 + age classes was examined by electrofishing 12 sections of a stream in Perthshire, Scotland at the end of the growing season in September to October in 1972 and 1976. In 1972 sections ranged in surface area from 21 to 122 m² and had volumes of 5.0–17.3 m³ and when surveyed in 1976 surface areas were 15–106 m² and volumes 2.1–6.7 m³. In 1976 widths and areas of sections were 63–87% of the values for 1972, depths were 39–68% and volumes 28–52% of the earlier values. These differences were due to 1976 being drier and warmer. In both years, all sections contained 0 + and 1 + age classes of salmon and trout and some sections contained 2 + age salmon and trout. The total density of fish in a section ranged from 1.9 to 3.9 m⁻² in 1972 and from 3.72 to 6.08 m⁻² in 1976. There was an inverse relationship, significant in 1972 only, between the density of 0 + salmon and that of 1 + trout in the different sections. Densities of both 0 + and 1 + salmon in the sections were inversely correlated, and those of 0 + and 1 + trout were directly correlated, with area of water deeper than 10 cm.     

Movements of brown trout, Salmo trutta, and juvenile Atlantic salmon, Salmo salar, in a coastal stream in northern Norway

Movements of resident brown trout (age 2+ to 9+ years) and young Atlantic salmon (age 1+), stocked as fry, were studied in July, August and September in a coastal stream in northern Norway. Between 85 and 89% of the brown trout were recaptured in the study area (346m, 1326m²) within 45m of their release point throughout the investigation period. Most specimens had moved less than 150m. Trout movements were related to local variation in density. Trout occupying those sections of stream with the lowest fish densities (5.3–10.9 fish 100m^?2) had a significantly lower movement rate than fish from sections with densities between 13.7 and 31.5 fish 100m^?2. Trout that moved from their marking section were significantly larger than specimens that did not leave their original site. There was a significant correlation between permanence of station each month and the mean water level that month. The majority of the trout (47%) were caught at undercut stream banks or at sites in the proximity of these. A decrease in water level during the study period resulted in a high loss (36%) of such habitat, probably forcing some individuals to move. The recapture data indicate that the trout population consists of one small (c. 15–20%) mobile, and one large sedentary component. Young salmon displayed high station permanence in July and August (93% and 96%). However, in the autumn they exhibited a significant downstream movement, and only 73% were recaptured within their release section. This movement was significantly higher for larger specimens, and is thought to occur because of a pre-winter change in habitat, initiated by a decline in stream temperature. In contrast to trout, salmon in sections containing the lowest densities (22.0–25.0 fish 100m^?2) did not show significantly lower movement rates when compared with salmon at higher densities (32.2–46.3 and 51.8–60.6 fish 100m^?2). The spatial distribution of young salmon indicated the formation of territorial mosaics over the stream bed, which are thought to reduce intraspecific competition.     

Production of juvenile Atlantic salmon, Salmo salar L., and brown trout, Salmo trutta L., within different sections of a small enriched Norwegian river

Growth, density and production of juvenile Atlantic salmon and brown trout were studied in three different sections of the Kvassheimsåna River in south-western Norway from 1979 to 1983. Section 1. in the upper part of the river, is located above a waterfall impassable for migratory salmonids and is surrounded by grazing land. Sections 2 and 3, in the middle and lower parts of the river, are influenced by agricultural activity. Total nitrogen concentration varied between 250 and 1000 μg l ^?1 in section 1 and 1500 and 2500 μg l^?1 in sections 2 and 3. Total phosphorus (Tot-P) concentrations also increased with decreasing altitude: 19–46 μg l^?1 in section I and 31–101 μg l ^?1 in sections 2 and 3. The number of 0 + salmon in sections 2 and 3 varied between 30.1 and 167.8 specimens 100 m ^?2, with means 90.2 and 95.2 specimens 100 m ^?2:, respectively; the density of 1 + salmon, with mean values of 16.3 and 51.0 specimens 100m^?2 was significantly correlated with the original fry density. The growth rate of 0+ salmon was not inversely related to cohort density, but was significantly so for 1 + salmon. Mean annual salmon production in section 2 was 1595 g 100 m^?2 year ¹, and in section 3 was 841 g 100m^?2 year ¹. A logarithmic function gave the best curve fit between salmon production and mean annual biomass. Thus, production levelled off for the highest values recorded in section 2, and perhaps approached the carrying capacity of the stream. A multiple regression analysis showed that yearly variation in 1 + salmon density was the single factor accounting for most of the total variability in production (60%). Variation in water temperature and nutrient content were not significantly related to variation in fish production. Densities of brown trout were low in all sections (<20 specimens 100m ^?2). Fry density was highest in section 3 and parr density in section 1. All age groups of sympatric brown trout grew significantly faster in sections 2 and 3 compared with allopatric brown trout in section 1.     

Seasonal and regional infestation characteristics of three ectoparasites of whiting, Merlangim merlangus L., in the North Sea

The colonization by both resident and migrating spawner populations of brown trout and the characteristics of resident and migrating juveniles derived from the two populations have been studied in a brook and its tributary over 4 years. Resident trout spawns mainly in the upstream part of the brook and migrating trout in the downstream part. There are density and growth variations for the two age classes (0+ and 1 +) of juveniles in autumn according to the year and the environment. In the brook, the population of 0 + fish increases from downstream to upstream while the density of other age classes decreases. The migrating juvenile population of the brook changes annually and consists mainly of 1 s (one summer) individuals coming from the upper part. These individuals migrate generally in autumn and winter while young trout produced in the middle and downstream parts of the brook migrate mainly in the spring. The emigration process of the 0 + population decreases markedly from upstream to downstream and appears to be independent of the autumn length and sex ratio. In the tributary, most trout are 0+ years old, the population structure is different, and no migrating fish is observed. The results are discussed and a colonization strategy of the brown trout population in this brook is suggested.     

A survey of the macro-fauna of the River Cynon, a polluted tributary of the River Taff (South Wales)

(1) A survey of the macro-invertebrates and fish in the River Cynon, a trout stream in south-east Wales receiving industrial and domestic wastes, and nine of its tributaries, was carried out in the summer of 1970. Its principal purpose was to describe the structure of these communities before waste treatment facilities, in course of construction, reduce the degree of pollution. (2) The macro-invertebrate communities changed dramatically at station C4, there being a very varied fauna upstream and one dominated by chironomids and oligochaetes downstream, principally Nais barbata., Cricotopus bicinctus and Syncricotopus rufiventris. It seems likely that coal particles, influencing the substrate, are largely responsible for this change. Further downstream, and below substantial organic discharges, tubificids and the enchytraeid, Lumbricillus rivalis, became increasingly abundant. The total density of macro-invertebrates increased from about 2000/m2 in the headwaters to over 20,000/m2 in the lower reaches. (3) The fauna of the clean tributaries, Hir (C16) and Wenallt (C19) was similar to that ofthe unpolluted upper reaches ofthe Cynon (C1-C3) whereas that of tributaries affected by coal particles was similar to the fauna of the Cynon downstream of C4. (4) Six species of fish were recorded (bullhead, eel, minnow, trout, stickleback and stoneloach) of which tbree (bullhead, eel and trout) were confined to reaches upstream (C8 and above) of industrial eflluents at Abercwmboi. For 0–8 km downstream of these effluents the river was fishless and further downstream, to the confluence with the River Taff, fish density and biomass were reduced. (5) In the upper Cynon and its tributaries the density and biomass of trout were within the range recorded elsewhere in the British Isles. The growth rate of trout in the catchment is low. Diflerences in growth rate and shape of trout in the main river and tributaries suggest that there is little interchange between these areas, except perhaps with very young fish. 0 + * * The convention of referring to fish in their first year as 0+, in their second year as 1 + and so on is adopted here.
fish were only caught in abundance at two tributary stations and their numbers, even if widely distributed, could not permanently support the current density of older fish throughout the upper catchment. (6) Stone loach and minnow reached a very large size and individuals caught of the latter species approached the maximum recorded length for the British Isles.     

Recolonisation potential of zooplankton propagule banks in natural and agriculturally modified sections of a semiarid temporary stream (Doñana,Southwest Spain)

The viable propagule banks of a temporary stream were studied from sections with different agricultural history. Hatching of zooplankton (copepods, rotifers and cladocerans) was recorded in the laboratory under controlled temperature and light conditions from an agriculturally modified area with average hydroperiods of about a week per year and two semi-natural reference areas with average hydroperiods of more than 3 weeks per year. We found significant differences in both taxon richness and abundance of zooplankton hatching between areas, which were lower in the agriculturally modified section, compared to the reference sections. Another factor likely to have influenced hatching in our experiment was conductivity, which differed between the two reference sections and might have affected hatching at high conductivities. For restoration purposes, hydrological reconnection of stream segments is important to facilitate dispersal from the high diversity upstream segments to the depleted sites downstream.     

Age and growth of Siberian sculpin (Cottus poecilopus) and young brown trout (Salmo trutta) in a subalpine Norwegian river

Age, growth and density of Siberian sculpin (Cottus poecilopus) and young brown trout (Salmo trutta) within two sections of River Atna; above Lake Atnsjøen [Section 1 at altitudes between 739 and 715 m] and below Lake Atnsjøen [Section 2 at altitudes between 430 and 370 m] was studied during a 6-year period (1986–91). The water temperature was considerably lower in Section 1 than in Section 2, as the number of days with a water temperature above 10?°C (T _{D ≥ 10?° C} ) from spring to August 1 ranged between 2–26 and 26–52 days, respectively. Juvenile brown trout (age 0+) attained a significantly smaller body size in Section 1 than in Section 2; mean length ±SD was 35 ± 8 mm (ranged 27–46) and 43 ± 7 mm (range 38–46), respectively. In Section 2, there was a highly positive correlation between the body length of 0+ brown trout and mean water temperature in June (p<0.005), and also to some extent in Section 1 (p=0.11). Individuals of age 1+ did not exhibit any such difference, while fish in age group 2+ were larger in Section 1 than in Section 2. By using the number of days with a water temperature between the range 5–10?°C (T _{D ≥ 5 ? 10?° C} ) as test variables, we found a highly positive correlation between the August 1 body length of 0+ brown trout and T _{D ≥ 9}?°C from spring to August 1 in Section 2 (p<0.05), as opposed to T _{D ≥ 7}?°C for trout in Section 1 (p=0.11). Young Siberian sculpin (age 0+ and 1+) also exhibited slower growth in Section 1 than in Section 2, but this was not the case among older specimens. In the year with the lowest temperature measured (1987), no 0+ Siberian sculpin were caught in any of the two sections, indicating that low temperature affects their survival. Both species exhibited large spatial and temporal variation in density. Thus, data on abundance and growth sampled on one occasion at one site can not be regarded as representative for these two fish populations.     

Habitat exclusion and reduced growth: a field experiment on the effects of inter-cohort competition in young-of-the-year brown trout

Competition during the juvenile phase is a key process for regulating density in organisms with high fecundity. Juvenile density-dependent bottlenecks may become even more pronounced if several cohorts compete, but this has received relatively limited attention in previous literature. We performed a manipulation experiment in seven coastal streams to investigate the presence of inter-cohort competition, using habitat selection, body-size and density of newly emerged (age-0) brown trout (Salmo trutta) as response variables. The trout population (age ≥ 1 fish) was estimated using electro-fishing prior to the emergence of fry (April-May) and was either removed (manipulated sections) or maintained (control sections). Age-0 habitat selection was examined in June while density and body-size was evaluated in October (end of the growth season). We found that age-0 trout selected habitats that were located further from riffles (nursery habitats) in the absence of age ≥ 1 trout, suggesting a niche overlap between cohorts in the habitat dimension and, hence, that both inter-cohort competitive interactions and ontogenetic preference may influence habitat utilisation in the wild. Furthermore, we also found age-0 body-size to be significantly larger in manipulated sections and negatively related to its own density. We argue that competition from older cohorts influence the availability of age-0 feeding territories at the critical phase of emergence with secondary negative effects on age-0 growth. These results not only have implications for understanding the mechanisms of density dependence but can also provide valuable knowledge to the management of salmonid populations and their habitats in the wild.     

Stocking hatchery‐reared brown trout in different densities into a wild population – a comparison of growth and movement

In spring 2001 and 2002 a small stream was stocked with tagged hatchery‐reared yearling brown trout ( Salmo trutta ), in order to study their influence on the resident brown trout population. The stream was separated into six sections: two sections without stocking, two sections where stocking doubled the trout population and two sections where the fish population was quadrupled. The working hypothesis was that due to food limitation (competition) growth of the wild fish will be negatively influenced by stocking, and wild fish will be displaced by the (possibly more aggressive) hatchery fish. Surprisingly, growth rate of wild and stocked fish of the same age was similar and independent of stocking density. Two main reasons may be responsible for this finding: only a low percentage of the stocked fish remained in the stream, and food was not limited during summer. Only 12–19% of the stocked fish were recaptured after six months, in contrats to 40–70% of one‐year old and up to 100% of older wild trout. The wild fish were not displaced by hatchery‐reared fish: During summer the wild fish remained more or less stationary, whereas most of the stocked trout had left their release site. The results indicate that in a natural stream stocking of hatchery reared brown trout does not influence negatively growth and movement of the wild fish independent of stocking density.     

Growth and mortality of introduced fish larvae in a newly restored urban river

The potential of a newly restored river as a nursery for endangered rheophilic fish species was estimated by introducing a population of individually marked larvae of nase Chondrostoma nasus into two river sections differing in river morphology and hydrological conditions. After 12 months, clear differences in fish abundance and fish size were observed: in the braided floodplain section C. nasus were more abundant and larger in size than in the straight river channel section. Total mortality rates over the whole investigation period did not differ between the two sections.     

Physical characteristics influencing the utilization of pools by brown trout in an afforested catchment in Southern Ireland

Seasonal and spatial variation in brown trout Salmo trutta L. abundance, density and biomass were studied in 29 pools of varying size in an afforested catchment together with the physical characteristics of those pools. A movement of 0+ trout towards the pools as the year progresses was detected. Water volume of the pool accounted for a significant amount of the variation in metrics across all seasons. Cover provided by overhanging vegetation also explained a significant amount of variation, especially during the summer. Water velocity, percentage of undercut bank and substrate composition had little explanatory power in the distribution of trout in the pools. In all seasons significant relationships between both fish biomass (g m⁻²) and fish number and water volume in the pool were found. However, in summer and autumn there was also a significant correlation between both fish density (fish m⁻²) and biomass and water volume in the pool described by a power function with a coefficient >1. These relationships were consistent across the subset of pools studied over a 2-year period. Thus there was a proportionally greater number of fish in deeper pools than in the shallower ones in summer and autumn, suggesting that trout use the available habitat (i.e. the pool) as a three dimensional space in which an increase in the third dimension (depth) leads to a proportionally greater number of fish per unit area.     

Movement and population size of the river sculpinCottus hangiongensis in the Daitobetsu River of southern Hokkaido

Individual movements and population size of the amphidromous sculpinCottus hangiongensis, excluding young-of-the-year smaller than 50 mm in body length, were studied from October 1983 to December 1984 in 5 separate sections of the Daitobetsu River of southern Hokkaido, by using mark-recapture methods. During the non-breeding season, distinct inclinations in density, body length distribution and sex ratio ofC. hangiongensis populations were found along the course of the river. The population density was the highest, 3.45 per m², in the lowest section and decreased in the upper sections. Larger males were found in larger numbers toward the lower reaches, whereas the sex ratio, which was biased in favor of females, was generally more striking upstream. These characteristics of the population structure may result from the amphidromous life history and the polygynous mating system of this species. Many marked fish were recaptured within the original sections, where they had been marked and released, throughout the year. During the non-breeding season, especially, the mean movement was 40.6 m, with the greatest movement being 92 m. During the breeding season, on the other hand, some sculpins appeared to move downstream before spawning and upstream after spawning. Such downstream spawning migration may increase the chance of encountering a mate, and for females it may enhance the chance of encountering larger males. Moreover, it may also contribute to a decrease in the mortality rate of their flowing larvae.     

Brown trout spawning habitat selection preferences and redd characteristics in the Credit River, Ontario

Brown trout Salmo trutta redds in the Credit River, Ontario, were enumerated and assessed for physical, location and cover feature characteristics during the 2002 spawning season. Hydraulic habitats were classified on the basis of channel morphology and availability recorded. Combined use and availability data were used to assess habitat selection preferences and test for significant differences. Significant preferences for upstream pool and riffle habitat were found, but all available habitat types were used to some degree. Non‐preferred habitat redds were significantly larger than those located in preferred habitats and more likely to be found in association with woody debris cover. Larger redds were interpreted as indicative of larger fish. The use of non‐preferred downstream habitats by larger fish was further interpreted in the context of overwinter habitat requirements to reflect possible trade‐offs between reproductive and adult over‐winter survival requirements resulting in the selection of habitat for multiple life‐history functions. Results suggest that redd density alone should not be used to infer critical autumn habitat requirements for brown trout.     

Effects of Fish-farm Activity on the Limnetic Community Structure of Brown Trout, Salmo trutta, and Arctic Charr, Salvelinus alpinus

Establishment of four fish-farms during the period 1971 to 1994 in the oligotrophic lake Skogseidvatnet affected Arctic charr, Salvelinus alpinus, but not brown trout, Salmo trutta. From 1971 to 1987, an increase in mean individual size of Arctic charr was recorded, while the mean individual size of brown trout remained stable. Arctic charr were found to use deeper benthic areas than brown trout. Approximately 8% of the Arctic charr population (>26cm), were found to switch to waste food from fish-farms, resulting in a novel feeding habitat for the species. They were, however, found in gillnets distant from the fish farm cages, indicating high mobility. The habitat segregation between the two species can most likely be explained by selective differences and asymmetric competition with brown trout as the dominant species. Based on the present results, changes in the Arctic charr population may be due to increased food availability and due to a new habitat use as a waste food feeder. The reason for the brown trout population to have remained stable with respect to mean size, growth pattern and habitat use, may be due to a different diet choice than Arctic charr in this lake. Brown trout were found to feed mainly on terrestrial insects, while Arctic charr fed mainly on zooplankton and on waste food.     

A 27-year study of brown trout population dynamics and exploitation in Lake Songsjøen, central Norway

From 1968–1984 (period I), a brown trout Salmo trutta , population in a 70-ha oligotrophic lake in central Norway was exploited using larger mesh gill-nets selectively removing the larger fish. From 1985–1994 (period II), intermediate sized fish were removed using smaller-mesh sizes gill-nets. Fishing mortality and CPUE were correlated positively with effort and numbers of fish >3 years old for period II. The gill-net catchability was correlated negatively with spawner biomass and number of trout >3 years old. The significant positive correlation between natural mortality and stock biomass and spawning stock biomass indicated density-dependent mortality. The significant correlation between spawning stock and recruitment described by the Ricker model, indicated density-dependent recruitment of 1-year-old trout. The fishing regimes in the two periods affected the population dynamics and density differently. Selective removal of smaller fish permitted the larger fish to survive, and was beneficial in reducing fish density and maintaining stocks at low levels, consequently, achieving the expected increase in fish growth rates.     

Growth, survival and production of juvenile salmon and trout in a Scottish stream, 1966–75

Investigations of the growth, survival and production of young salmon Salmo salar , brown trout and sea trout S. trutta in sections of a stream in Scotland were made during 1966–75. At the end of the growing season, in autumn, the size of the 0+ salmon ranged from a mean weight of 1.12 g in 1966 to 2.82 g in 1973, and the size of the 0+ trout ranged from a mean of 2.20 g in 1966 to 3.56 g (68.0 mm) in 1974. Growth rates of 0+ salmon between July to September were similar from year to year, as was the case with the 0+ trout. The greater size attained in their first year by trout, resulted from the longer feeding season, provided by earlier emergence of fry and ability to continue growing in colder weather in autumn. The lengths attained by 0+ salmon and 0+ trout in September were related to the population densities of 0+ salmon and the number of days above 0° C from 1 December. There was no discernible relationship between lengths of 0+ trout and the population densities of 0+ trout. Salmon and trout lost weight during the winter, which was made up by April. The densities of 0+ salmon in June varied between 2–12m ^–2. Rates of decrease of the population densities in their first year were related to their densities at the beginning of the season, and, more closely, to the densities of salmon and trout combined. At the end of the second year's growth there were between 0.06 and 0.25 salmon m ^–2. Size of the trout populations varied less from year to year than those of salmon. The life of a year class of salmon and trout could be divided into several stages characterized by different rates of decrease of the population.     

Density‐dependent and density‐independent growth in a population of juvenile sea‐trout,Salmo trutta,assessed using long‐term data from a small stream in Northwest England

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