Susceptibility of brown trout to Gyrodactylus salaris (Monogenea) under experimental conditions

Brown trout ( Salmo trutta ) from anadromous River Lierelva, resident Lake Tunhovd, and resident Nordmarka stocks were exposed to Gyrodactylus salaris -infected salmon parr. The brown trout were fed pellets before the experiments, except for one group of the Nordmarka stock which was starved for 19 days before the experiments. The mean number of parasites declined directly and rapidly post infection for all groups of trout. There were no pronounced differences in resistance between the anadromous and the resident stocks. G. salaris infections tended to persist longer on starved than on fed trout of the Nordmarka stock. The maximum parasite persistence on trout was 50 days, and as parasite numbers increased on some fish parasite reproduction must have occurred on those trout. However, the limited susceptibility and marked innate resistance of trout to G. salaris establishment, development and reproduction, suggest parasite metapopulations will not survive on this species. Nevertheless, trout may still play a role in the dispersal of G. salaris within and between rivers.     

Differences in feeding between 1+ and 2+ hatchery brown trout exposed to low water temperature

Both 1 + and 2+ brown trout fed during the day and at night when held in hatchery tanks at low temperatures (2·7–3° C). Over 60% of the daily ration was consumed during daylight hours, but there were differences in feeding behaviour between fish of the two age groups: the 1 + trout had greater feeding activity at night than the 2+ fish.     

Association between growth, body condition and anti-predator behaviour in maturing and immature brown trout parr

In spring there were significant differences between maturing and immature brown trout Salmo trutta in anti-predator behaviour to pike and heron models when all behaviours were combined in multivariate analysis. However, the time until the trout visited the patch in the experimental tray where predators attacked was the only variable that alone significantly differed between maturity groups; following transfer between the rearing tank and the experimental tray, maturing fish visited this patch sooner. The difference in anti-predator behaviour coincided with differences developing between the groups in both growth rate and condition factor. Maturing fish showed higher growth rates and exceeded immature fish in condition factor from spring onwards. In a summer experiment, no differences in anti-predator behaviour were observed between maturing and immature fish. It is concluded that increased risk-taking to facilitate higher food intake is probably the behavioural mechanism responsible for the comparatively greater increases in growth and body condition observed among maturing fish in spring.     

Temporal variations of genetic introgression in stocked brown trout populations

Allozymes were used to analyse the genetic impact of hatchery brown trout Salmo trutt a, morpha fario stocked in wild Mediterranean populations to gain a better understanding of the mechanisms of introgression (regulation, elimination or homogenization). Analysis of the genetic structure of populations from the same river drainage basin but subjected to different incidences was performed in space and time (data on two generations and 2 years of sampling). Introgression is associated with high deficits of heterozygotes and linkage disequilibria. Genetic divergence according to age group was observed. These results may indicate selective forces acting against domesticated genes and limiting hybridization between the two forms.     

RNA-DNA ratios in white muscle tissue biopsies reflect recent growth rates of adult brown trout

Recently developed fluorescence techniques were used to quantify RNA-DNA ratios in white epaxial muscle tissue biopsies taken from live adult brown trout. RNA-DNA ratios from small biopsies (4–24 mg wet weight) were measured concurrently with growth over 5 weeks in two groups of brown trout fed different rations, 5% BW day^{– 1} (reference) and 1% BW week^{– 1}(treatment). Reduced rations had significant effects on RNA-DNA ratios in muscle tissue biopsies. The treatment group had significantly lower mean RNA–DNA ratios than the reference group after the first week. After 5 weeks of treatment the mean RNA–DNA ratios of the treatment and reference groups were 1–98 and 4–31, respectively. RNA-DNA ratios from muscle tissue biopsies reflected recent growth rates in the two groups of fish. This technique allows a biochemical measurement of growth rates in adult fish without mortality.     

Genetic structure of two Turkish brown trout populations

The genetic structure of two brown trout Salmo trutta populations living in Lake Abant in Bolu and Üzüm River in Antalya was determined by examining 15 enzyme coding loci ( AAT, ADH, LDH, MDH, MEP, GPI, PGM and SOD ) using starch gel electrophoresis. Population specific mobilities were observed for the fixed alleles of LDH-B2, mMEP-2 and SOD-1 loci. Polymorphisms in sAA T-4, GPI-B2 loci were observed within the populations. Average heterozygosity of Abant and Antalya populations was 0.0358 and 0.0224 respectively. For LDH-C which is the post glaciation marker locus, the ancestral allele * 105 was found to be fixed in both of the populations. Nei's genetic distance between the two populations was 0.2507 which is the level of genetic distance often found between different species. This difference seems to be due to the presence of unique alleles in the LDH-B2, mMEP-2 and SOD-1 loci of the Abant population, indicating that the conservation of the Abant population and its heterozygosity is of prime importance.     

Differences in growth between offspring of anadromous and freshwater brown trout Salmo trutta

In this study, individual growth of juvenile offspring of anadromous and freshwater resident brown trout Salmo trutta and crosses between the two from the River Imsa, Norway, was estimated. The juveniles were incubated until hatching at two temperatures (±S.D. ), either 4.4 ± 1.5°C or 7.1 ± 0.6°C. Growth rate was estimated for 22 days in August–September when the fish on average were c. 8 g in wet mass, and the estimates were standardized to 1 g fish dry mass. Offspring of anadromous S. trutta grew better at both 15 and 18°C than offspring of freshwater resident S. trutta or offspring of crosses between the two S. trutta types. This difference appears not to result from a maternal effect because anadromous S. trutta grew better than the hybrids with anadromous mothers. Instead, this appears to be an inherited difference between the anadromous and the freshwater resident fish lending support to the hypothesis that anadromous and freshwater resident S. trutta in this river differ in genetic expression. Egg incubation temperature of S. trutta appeared not to influence the later growth as reported earlier from the studies of Atlantic salmon Salmo salar.     

Survival and growth of sea trout parr in fresh and brackish water

There was no di.erence in survival or growth rate over 63 days for young-of-the-year sea trout Salmo trutta in fresh and brackish Baltic Sea water (6·7 psu). Hence, such sea trout parr that migrate from the freshwater habitat in which they hatch to the Baltic coastal zone, without smolting, should experience little or no physiological cost in survival and growth.     

Changes in some endocrinological and non-specific immunological parameters during seawater exposure in the brown trout

The influence of autumnal progressive and direct seawater transfers on ionic parameters, plasma growth hormone (GH) and thyroid hormones (TH) and also on the non–specific immune traits phagocytic activity, lysozyme and non–specific cytotoxicity were examined in 45–55 g brown trout ( Salmo trutta ). In both experiments, the seawater transfer induced the same pattern of endogeneous modifications but they were more pronounced and more lasting after the direct seawater transfer than after the progressive one. In seawater–transferred trout, there was a significant transitory increase of the plasma osmolarity, chloride concentration, GH levels and a transient decrease of the TH. The phagocytic activity of the pronephric leucocytes and the lysozyme concentrations were significantly higher in seawater–transferred trout than in controls. Nevertheless, the non–specific cytotoxicity should not be modified after the seawater exposure. Moreover significant positive correlations were observed between plasma GH and chemiluminescence or lysozyme increases. These data support the hypothesis that GH is involved in the salmonids' non–specific immune potential, especially by stimulating the macrophage functions.     

Structural complexity in the hatchery rearing environment affects activity,resting metabolic rate and post-release behaviour in brown trout Salmo trutta

The effects of structural enrichment in the hatchery rearing environment of brown trout Salmo trutta was linked to post-release performance. Enrichment resulted in reduced swimming activity scored in an open field test and reduced movement in a natural river after release. Also, enrichment increased resting metabolic rates, which correlated positively with overwinter growth.     

Prey orientation in piscivorous brown trout

Piscivorous brown trout Salmo trutta change their feeding behaviour depending on prey species, prey size and number of prey eaten. In trout which had eaten fish recently, most had one fish in their stomach, but up to 16 prey fish were found. Individuals of the small-sized minnow Phoxinus phoxinus were swallowed chiefly tail first, whereas individuals of the larger Arctic charr Salvelinus alpinus were taken both head and tail first. The largest charr were swallowed head first. In stomachs containing more than one fish prey, prey orientation was likely to be mixed. For all three types of prey orientation (i.e. tail first, head first and mixed), significant and positive correlations existed between prey length and predator length. The maximum prey size eaten tail first or in mixed orientation was about 70–85% of the size of prey eaten head first, indicating morphological advantages in eating the prey head first.     

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.     

Suboptimal growth among individuals of brown trout (Salmo trutta) in a temperate river

This study assessed growth of individually tagged brown trout Salmo trutta in a temperate system of north-west Spain (2010–2012). This study identified notable individual variation in fish growth with individuals growing sub-optimally compared with laboratory-based growth-model predictions in most cases (85.5% of individuals). The present observations of suboptimal growth need to be considered in view of intraspecific competition or limiting food resources instead of thermal regimes.     

Characteristics of brown trout males influence growth and survival of their offspring

Half-sib groups of juvenile brown trout Salmo trutta (0+ years) having fathers with different characteristics were compared in several respects. Two kinds of experiments were performed, aquarium observations in the laboratory and stocking in a semi-natural stream. It was found in the aquarium experiments that the offspring of fathers with larger adipose fins were more active and were probably better at defending territories. Offspring of males chosen by females had higher growth rate. The feeding rate was higher in juveniles having a less aggressive father or a father that was chosen by the mother. The stream experiments showed that offspring of dominant males had higher growth rates, and that offspring of less aggressive fathers had higher survival. Thus, characteristics of the males (fathers) influences the quality of the offspring, and there seem to be benefits for the females both to choose among potential mates and to spawn with the most dominant male. As these male characteristics are never regarded during the process of artificial breeding in hatcheries, the results indicate a basis for divergence between hatchery and wild populations.     

Variations in feed intake and growth of Baltic salmon and brown trout exposed to continuous light at constant low temperatures

Interindividual variations in feed intake and growth were studied in Baltic salmon Salmo salar and brown trout S. trutta , held under constant low temperatures of 2, 4 or 6° C and continuous light for 2 months. Rates of feed intake and growth were dependent upon rearing temperature, being lowest at 2° C and highest at 6° C. Further, feed intake and growth were initially low, but increased during the course of the experiment in both species and at all temperatures. These results suggest that acclimatization to the rearing conditions may have required several weeks. The increase in group mean feed intake with time was the result of both an increase in the proportions of fish that fed and an increase in feed intake amongst feeding fish. At the same time as feeding and growth rates increased, interindividual variations in feed intake and growth tended to decrease, suggesting that individual fish were acclimatizing to the new rearing conditions at different rates. Thus, the differences in group mean feed intake and growth rates observed at a given temperature reflected interindividual variations among fish making up the groups. This suggests that group rates of feed intake and growth are not only temperature- dependent, but that they are also highly influenced by variability among fish making up the group.     

Growth and social interactions of wild and sea-ranched brown trout and their hybrids

A laboratory study of the social behaviour and growth performance of juvenile brown trout Salmo trutta of wild and sea-ranched origin and their crosses, indicated that the social behaviour of wild and sea-ranched fish differed. Male and female parents seemed to have a different impact on the juveniles. The category having wild mother and sea-ranched father were less aggressive, less active in general, but active in feeding, and therefore had higher growth rates. This pattern arose despite that the feeding rate and the motivation to first get a food item when food was provided did not differ between the groups of fish. Wild fish tended to be most aggressive. If sea-ranched and wild fish have different intrinsic (genetically based) 'life styles', the crosses between wild and sea-ranched fish indicate that there is likelihood for an introgression of genes adapted to hatchery environment into the genetics of wild conspecifics. This is particularly serious when hatchery-reared fish invades wild populations over many years.     

Prey consumption rates and growth of piscivorous brown trout in a subarctic watercourse

Prey consumption rates of piscivorous brown trout Salmo trutta were studied in the Pasvik watercourse, which forms the border between Norway and Russia. Estimates of food consumption in the field were similar to or slightly less than maximum values from a bioenergetic model. The piscivore diet consisted mainly of vendace Coregonus albula with a smaller number of whitefish Coregonus lavaretus . Individual brown trout had an estimated mean daily intake of c . 1·5 vendace and 0·4 whitefish, and a rapid annual growth increment of 7–8 cm year⁻¹. The total population of brown trout >25 cm total length was estimated as 8445 individuals (0·6 individuals ha⁻¹), giving a mean ±  s . e . annual consumption of 1553880 ± 405360 vendace and 439140 ± 287130 whitefish for the whole watercourse. The rapid growth in summer of brown trout >25 cm indicated a high prey consumption rate.     

Influence of water quality, habitat and species richness on brown trout populations

The influence of water quality, physical habitat and species richness on the occurrence, density and size of brown trout at 216 stream sites in southern Sweden was studied. Discriminant analysis showed that the occurrence of trout at a locality was largely determined by oxygen conditions and medium-sized substrata. At localities where trout occurred, the density of + trout was highest in narrow streams with high oxygen concentrations. For older trout, >0+ in age, stream size and temperature were negatively related to density. Biotic factors also appeared to affect trout density, as trout density was inversely related to abundance of predators and coexisting species. Even intraspecific competition appeared to be important as length of 0+ trout was inversely related to trout density. It is suggested that improvements of water quality may be an effective way to restore sea trout populations in southern Sweden, especially in narrow streams where smolt production has the highest potential.