Influence of environmental factors on the density and biomass of stocked brown trout, Salmo trutta L., parr in brooks affected by intensive forestry

Abstract The influence of environmental factors on the density and biomass of stocked brown trout, Salmo trutta L., parr was studied in brooks subjected to intensive forestry in the Isojoki river basin, western Finland. Multivariate regression analysis showed that 69% of the variation in the population density of parr was determined by five variables: (1) mean water depth; (2) the abundance of pools; (3) stony bottom substrates with stones sized between 2 and 10cm in diameter; (4) undercut banks; and (5) the percentage of shading by trees. Correspondingly, 57% of the variation in the biomass of parr was determined by three variables: (1) mean water depth; (2) the abundance of pools; and (3) benthic vegetation. Dredging of the brooks and forest ditching had the most harmful consequences for the nursery habitats of brown trout parr. Measures for the rehabilitation of brown trout production in these brooks are discussed.     

Downstream migration of European lake trout, Salmo trutta f. lacustris L., and resident brown trout, Salmo trutta f. fario L., progeny in a Lake Constance affluent river

Abstract The local migratory behaviour of lake trout, Salmo trutta L., and resident brown trout, S. trutta L., progeny from an inflowing stream of Lake Constance was compared. No differences were detected with respect to emigration rate (3.5% and 4.2% for lake trout and resident trout, respectively), rate of residency (6.8% and 8.2% for lake trout and resident trout, respectively) and rate of survival (12.3% and 12.1% for lake trout and resident trout, respectively) one year after stocking. Some of the resident brown trout offspring became migrants and vice versa . The results indicate that the progeny of riverine brown trout contribute considerable numbers to lake trout stock.     

Incidence of hybridization between Atlantic salmon, Salmo salar L., and brown trout, Salmo trutta L., in Ireland

The substantial growth of the farmed salmon industry in Europe since the 1970s has highlighted concerns regarding the genetic impact of escaped farmed salmon on wild salmonid stocks. High incidences of salmon × trout hybrids have been recorded in rivers situated near intensive salmon farming in Norway and Scotland, which may be indicative of a breakdown in reproductive isolation between salmon, Salmo salar L., and brown trout, Salmo trutta L. In the present study, salmonid fry and 0+ parr were collected from rivers in western Ireland. Allozyme and minisatellite DNA analysis were carried out on fry to determine the frequency of F1 hybrids from 10 rivers located within 38 km of salmon farms and three rivers at least 80 km from salmon farms. A total of 49 hybrids were recorded from 4135 salmonid fry (frequency = 1.2%). Mitochondrial DNA analysis showed that all hybrids arose from Atlantic salmon female × brown trout male crosses. Hybrid parr were recorded from one of the low-risk rivers (1.0%), but were present in seven out of the 10 catchments located within 38 km of salmon farms, with frequencies ranging from 0.7% to 3.1%. The results of the present survey, which represents the first extensive record of the levels of salmon-trout hybridization in Ireland, are discussed in relation to the continued growth of salmon farming in this country.     

Growth and feeding responses of a hatchery population of brown trout (Salmo trutta L.) at low temperatures

Abstract— Feed intake, specific growth rate and changes in body composition were studied in age 1+ (140-190 g) brown trout ( Salmo trutta L.) reared at three temperatures (2, 4 and 6°C) under continuous light conditions. Feed in take increased from 35.7 kJ-kg⁻¹.day⁻¹ at 2°C to 95.7 kJ-kg⁻¹-day⁻¹ at 6°C, and the growth rate increased from 0.19%-day⁻¹ to 0.42%-day⁻¹ over the same temperature range. The estimated lower temperature limits for feeding and growth were slightly above 0°C. For all groups of fish, the majority (about 75%) of the weight gain comprised water and protein, but lipid deposition tended to increase with increasing temperature. The deposition of lipid accounted for about 50% of the body energy gain at all temperatures.     

Atlantic salmon, Salmo salar L., and sea trout, Salmo trutta L., passage in a regulated northern river – fishway efficiency, fish entrance and environmental factors

The number and the size of Atlantic salmon, Salmo salar L., using the Isohaara fishway was elevated by increasing the fishway discharge and by changing the type of the pass entrance. The fishway is intended to help fish bypass a hydroelectric station located close to the mouth of the large, regulated River Kemijoki, in northern Finland. Multi-sea-winter (MSW) salmon returned to the river mouth during peak flows in early June but did not use the fishway until 1 month later. Their number in the fishway was positively correlated with the tailwater level. One-sea winter (1-SW) salmon, which arrived approximately one month later, started to enter the fishway without corresponding delays. In autumn, a high tailwater level and a small drop at the fish entrance seemed to be needed for the successful passage of these small-sized salmon and sea trout, Salmo trutta L.     

Recaptures and resource use of native and non-native brown trout, Salmo trutta L., released in a Norwegian lake

Abstract Rate of recapture (gill netting), habitat use, and diet of three strains of stocked brown trout, Salmo trutta L., were compared with resident brown trout in a Norwegian lake. The strains originated from an alpine lake, from a boreal lake, and from the native brown trout population in the lake. Overall recapture rate was 5–8% for all strains. The low recapture rate could be due to the relatively small size at stocking; mean fish length varied between 13.1 and 14.5 cm with strain and stocking method. Two years after release, the frequency of the different strains decreased from about 12% in the first year to stabilize at about 1%. The alpine strain showed the highest overall recapture rate, whereas the native strain was recaptured at an intermediate rate. The overall recapture rate of scatter-planted brown trout was higher than that of spot-planted brown trout. Immediately after being stocked, introduced fish ate less and had a less-varied diet than resident trout; however, stocked fish adopted a natural diet within the first summer. The distribution of trout between the pelagic and the upper epibenthic habitat was similar for both the resident and the stocked brown trout. Results indicate that the habitat use of stocked brown trout is adaptive and becomes similar to that of indigenous fish.     

Stocking of brown trout, Salmo trutta L.: effects of acclimatization

One-year-old hatchery brown trout, Salmo trutta L., ( n  = 16 520) from a sea-run, local brood stock were marked and released (scatter-planted) into the River Laisälven in northern Sweden. Eight different groups were created using Alcian blue and Visible Implant Elastomer tags. Half the fish were kept in small enclosures in four stocking areas for 6 days before release. The other half were released just after transportation. To evaluate the effect of acclimatization on post-stocking performance, the areas were electric fished 2 months later. During the electric fishing survey, a higher number of the acclimatized hatchery fish were recaptured than those released immediately. The growth rate of stocked fish differed significantly between stocking areas and fish held in enclosures grew more than those released directly. The rate of recapture of hatchery fish varied between stocking areas (6.4–17.4%). Movements of juveniles within and between the stocking areas were low, and only 3.6% of the recaptured fish were found in an area not originally stocked. These results showed that acclimatization of fish before release increases the number and size at recapture within a stocking area.     

The effects of lakes on growth in yearling brown trout (Salmo trutta L.)

Abstract– Data from the Swedish Electrofishing Register were used to study the effects of lakes on the growth of yearling (0+) brown trout in outlet streams. It was found that growth increased close to lakes. On average, the length of the longest yearlings was 10% greater 0-100 m downstream from lakes as compared with more than 1 km downstream. Growth enhancement was most pronounced downstream from large lakes. This was exemplified with maximum yearling lengths in September in inlet streams (maximum yearlings 50-100 mm) and outlet streams (65-130 mm) of Lake Stora Le (area 200 km²), and inlet streams (50-75 mm) and outlet streams (65-95 mm) of Lake Anten (area 18 km²). It is suggested that this is a combined effect of both increased water temperature and outflow of lake seston. The growth pattern found was not correlated to population abundance or to the abundance of competitors or predators.     

Effect of habitat type on growth and diet of brown trout, Salmo trutta L., in stream enclosures

The effect of habitat on the growth and diet of brown trout, Salmo trutta L., stocked at the same densities in nine stream enclosures, comprising three habitat types of different quality, were tested. The habitats, which were created based on microhabitat preference data, were a shallow water habitat lacking cobbles (habitat 1), a deeper, mixed cobble-bottomed (128-384 mm diameter) habitat (habitat 2) and a large cobble-bottomed (256-384 mm) habitat of intermediate depth (habitat 3). Brown trout were found to have greater increases in total biomass in habitats 2 and 3 than in habitat 1. The pattern for length did not follow that of biomass as trout had greater increases in total length in habitat 2 than in the other two habitats. Biomass of food in trout diets reflected habitat-specific fish biomass changes, with a greater total biomass of prey as well a greater biomass of the leech, Erpobdella, in habitats 2 and 3 than in habitat 1. There were no habitat-specific differences in the biomass of benthic or drifting invertebrates in the enclosures, with the exception of a tendency for an effect of habitat on the biomass of Erpobdella. Although there may have been habitat-specific differences in food resources that were not detected, it is believed that the higher biomass growth in habitats 2 and 3 may have reflected differences in cover afforded by the deeper water and coarser substrates and/or improved foraging opportunities facilitated by the larger volumes of water in the deeper habitats in which the trout could search for prey.     

Mesh selection in a sea trout, Salmo trutta L., commercial seine net fishery

Abstract The length distribution of adult sea trout, Salmo trutta L., from a commercial seine net fishery using a nominal minimum mesh size of 50 mm or 102 mm is described. The smaller mesh size captured sea trout larger than 210 mm whilst the larger mesh size caught sea trout mainly above 400 mm, with no fish below 320 mm. A sea trout length/ girth relationship is described, and coupled with biological data allowed the calculation of mesh sizes for the appropriate escapement of different sea ages of sea trout.     

Factors influencing the yield of brown trout, Salmo trutta m. lacustris L., in northern Finnish lakes

Abstract Lake-to-lake variation in brown trout, Salmo trutta m. lacustris L., yield from stocking was examined in 34 lakes in northern Finland. The trout were mainly stocked as 2–3-year-old fish. Catch statistics were compiled with information on water quality, water level fluctuations, fishing effort and lake geomorphology. Absolute brown trout yields (kgha^-1) increased with increasing stocking rate, but there was an indication of non-linearity at higher stocking densities. Relative yields (kg per thousand trout released) were highest at low stocking rates. Stepwise multiple regression analysis was used to determine the best predictive model for lake-to-lake variability in brown trout yields. Seventeen measured regressands were used initially, and then replaced with scores obtained in a principal component analysis of highly correlated water quality variables and species-specific fish yields. Three major determinants of brown trout yields in these lakes were found in both analyses: fish community, stocking rate and fishing effort. Brown trout yields from stocking were higher in lakes with proportionally high yields of vendace or vendace and whitefish and proportionally low yields of pike.     

Migratory behaviour of brown trout, Salmo trutta L: importance of genetic and environmental influences

Lake Storvindeln in northern Sweden supports a population of fast-growing lake-run brown trout. Spawning and early rearing take place in the River Vindelälven, while most growth occurs in the lake (piscivory). A smaller tributary to the lake, Låktabäcken Creek, holds a resident, early maturing, short-lived brown trout population, although no migratory barriers have existed since 1947. To establish a lake-run trout population, fry from the migratory R. Vindelälven stock were introduced into the creek during 1985–1991. Introduced trout descended to the lake prior to maturing. As a result of the introduction, large adult trout returned from L. Storvindeln to the creek to spawn in 1991 and 1992; i. e., the introduced trout were able to complete a migratory life cycle. Genetic factors appeared to have a primary influence on the predisposition to migrate in this case, and it is suggested that migratory populations rarely develop from strictly resident ones.     

Do dams increase genetic diversity in brown trout (Salmo trutta)? Microgeographic differentiation in a fragmented river

Abstract – Local genetic differentiation may potentially arise in recently fragmented populations. Brown trout is a polytypic species exhibiting substantial genetic differentiation, which may evolve in few generations. Movement (semi‐)barriers in rivers may cause fragmentation, isolation and genetic differentiation in fish. In the Måna River (28 km) flowing from the alpine Lake Møsvatn to the boreal Lake Tinnsjø, construction of four hydropower dams during the period 1906–1957 have fragmented the previously (since last Ice Age) continuous wild resident brown trout population. Samples from the two lakes (N = 40) and six sites in the river (N = 30) isolated at different times were analysed at nine microsatellite loci. All populations showed substantial genetic variation (mean number of alleles per locus 5.3–8.9, observed heterozygosity 0.57–0.65 per population, overall F_st = 0.032). Pairwise multilocus F_st estimates indicated no significant differentiation between populations in the two lakes, and no or little differentiation in the lower river (F_st = 0.0035–0.0091). The microgeographic differentiation among wild resident trout at these sites was less than expected based on similar previous studies. However, results from the upper river, in particular the site immediately below the Lake Møsvatn outlet and dam, indicated isolation (F_st > 0.035). Calculation of genetic distances and assignment tests corroborated these results, as did a significant correlation between years of isolation (since dam construction) and F_st. The population structuring is most likely a result of fragmentation by dams, which has increased overall genetic diversity. This increased local differentiation may be caused by natural selection, but more likely by genetic drift in small, recently fragmented populations. Increased local genetic diversity by genetic drift does not justify conservation measures aiming at preserving genetic diversity.     

Artificial reconditioning of wild sea trout, Salmo trutta L., as an enhancement option: initial results on growth and spawning success

Abstract  Following a sea trout stock collapse in 1989 and 1990, wild sea trout kelts were successfully reconditioned in brackish water using semi-moist pellets and a commercial broodstock diet. The on-growing of wild sea trout smolts was not so successful. Natural mortality was 12.9%, and 36.1% of the fish failed to adapt to the artificial diets: 82% of these were smolts. Instantaneous growth was highest from June to August (0.74%), with an overall rate for April to September of 0.51%. At the end of the first year. 36 females and 26 males matured; 34 females, with a mean fork length of 33.2 cm, were stripped yielding 22860 ova at a mean rate of 682 ova per female or 1586 ova kg^-1 body weight. The survival of green ova to eyed ova was 90–98%, and survival from green ova to hatched alevin was 95%.     

Genetic characterization of Portuguese brown trout (Salmo trutta L.) and comparison with other European populations

Abstract– Allozyme and other protein loci were examined to study the genetic structure of Portuguese brown trout ( Salmo trutta ) populations. A total of 247 individuals from three tributaries of the Lima hydrological basin and a hatchery, all located in northern Portugal, were analyzed. Four of 22 protein coding loci were found to be polymorphic: CK-A1^*, GPI-A2^*, MPI-2^* and TF^*. A new allelc at the latter locus was found in Atlantic populations. The data obtained for Portuguese brown trout were compared with published data for 14 European populations and three hatchery stocks. Six polymorphic loci (CK-A1^*, GPI-A2^*, GPI-B2^*, LDH-C^*, ME^* and MPI-2^*) were used in a cluster analysis. This showed the similarity of Portuguese natural populations and northern Iberian populations and that Portuguese hatchery fish have an autochthonous origin, distinct from that of other Atlantic hatchery stocks.     

Recovery of Hafnia alvei from diseased brown trout,Salmo trutta L., and healthy noble crayfish,Astacus astacus (L.), in Bulgaria

Hafnia alvei was isolated in Bulgaria from healthy noble crayfish, Astacus astacus (L.), and then from farmed diseased brown trout, Salmo trutta L., with signs of haemorrhagic septicaemia. The isolates were identified initially with conventional phenotyping and commercial Merlin Micronaut and API 20E rapid identification systems, followed by sequencing of the 16S rRNA gene. Hafnia alvei Bt1, Bt2 and Aa4 were of low virulence to rainbow trout and brown trout, although cytotoxicity was demonstrated by Bt1 and Bt2, but not by Aa4.     

Genetic effects of introduced hatchery stocks on indigenous brown trout (Salmo trutta L.) populations in Spain

Abstract– To assess the levels of gene introgression from cultured to wild brown trout populations, four officially stocked locations and four nonstocked locations were sampled for one to three consecutive years and compared to the hatchery strain used for stocking. Allozyme analysis for 25 loci included those previously described as providing allelic markers distinguishing hatchery stocks and native populations. Different levels of hybridization and introgression with hatchery índividuals were detected in stocked drainages as well as in protected locations. These findings indicate that new policies for stocking and monitoring hatchery fish are needed if gene pools of wild Spanish brown trout populations are to be preserved.     

Population genetics of the European trout (Salmo trutta L.) migration system in the river Rhine: recolonisation by sea trout

Abstract –  Allozyme genetics (34 loci) is studied in up to 1010 European trout ( Salmo trutta ) from the Rhine, Meuse, Weser, Elbe and Danube river systems in Central Europe. Population samples from single collection sites, chiefly small streams ( G _CG = 0.2126), rather than the divergence of the trout from Atlantic and Danubian drainages ( G _SG = 0.0711), contributed to the overall gene diversity of G _ST = 0.2824. Sea trout ( n  = 164) and brown trout ( n  = 767) in Atlantic rivers adhere to the same biogeographical stock, but anadromous trout from the Rhine and the Elbe display more genetic cohesion than resident brown trout from the Rhine system alone. Strayers from the Elbe could have founded the recently re-established sea trout population of the Rhine, after a few decades of absence or precarious rarity. Migrants may even connect the Rhine and Elbe stocks by ongoing gene flow. A release–recapture study confirms that all trout in the Rhine belong to one partly migratory population network: Six of 2400 juvenile sea trout released into a tributary of the Rhine were later recorded as emigrants to the Rhine delta, against three of 1600 released brown trout. One migrant had entered the open North Sea, but the other dispersers were recorded in fresh waters of the Rhine delta (Ijsselmeer, Amstelmeer). Stocking presumably elevated both heterozygosity and fixation indices of brown trout, but this effect is subtle within the range of the Atlantic population group. Improved sea trout management in the Rhine, and modifications to brown trout stocking in the upper Danubian area are recommended.