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Notes: Hatchery reared 0+ year brown trout Salmo trutta, with 51 mm mean LT, were released in a sea trout stream in June 1991 to compare the survival of wild and introduced trout during the freshwater stage from age 0+ to 2+ years. The introduced brown trout were homozygous for a genetic marker, enabling released individuals and their offspring to be distinguished phenotypically from the local sea trout. The mean size of 0+ and 1+ year introduced parr was larger than 0+ and 1+ year wild parr, while 2+ year parr of both groups were of the same size. Half year survival rates of both introduced and wild parr increased with size up to c. 80 mm (1+ years), but then decreased, and could be described by a polynomial regression function, with the same shape for both groups. The introduced parr had, however, a significant lower survival rate than the wild parr. The number of the introduced cohort decreased from 2200 at release in 1991 to c. 20 in March 1994 (c. 1% of the original number). Between 1994 and 2000 no introduced individuals or offspring have been observed in the study area. High mortality at the parr stage and additional mortality until the spawning, give a low probability for a genetic impact on the local population as long as releases are restricted, both in time and number of fish.

Notes: Freshwater resident and anadromous life history forms of brown trout, Salmo trutta L., sampled from each of three watercourses were analysed for biochemical genetic variation. Ten enzyme systems encoded by a putative 30 loci were analysed. Significant genetic differences were found between the two life history forms in all three watercourses. Further, significant genetic differences were also found between the three anadromous populations analysed, although two of them are separated by a distance along the shore line by less than 2 km. The findings focus on the need to reconsider the conservation and management practice of wild and hatchery-reared stocks.

Notes: A study was undertaken to compare first-feeding mortality among 10 brown trout families fed high (100%) and low (25%) rations in replicate mixed family tanks. Microsatellite DNA profiling was used to assign individual brown trout to family of origin. At the end of the 35 day experimental period, highly significant differences in overall mortality were observed between the two treatments, and within the treatments there were highly significant differences in family mortality. Both replicates displayed similar patterns of family mortality. Notably, the distribution of mortality among families differed significantly between the two ration treatments, although this was more distinct for some families than others. No correlation between mean family egg diameter and family mortality were observed within either feeding treatment, although a significant positive correlation between mean family egg diameter and timing of family mortality was observed. It is suggested that these data indicate the existence of a genotype x environment interaction relating to feeding level during the critical start-feeding period.

Notes: Two experimental groups comprising mixed Norwegian sea run and freshwater resident brown trout Salmo trutta were infected with sea lice Lepeophtheirus salmonis in replicate tanks. Comparison of mean abundance and louse development between the sea run and resident groups revealed highly significant differences in lice abundance. The resident trout had an average abundance ± of 6·3±0·37 and 6·6±0·43 lice whilst the sea trout had an average abundance of 3·5 ±0·25 and 3·3 ±0·28 lice 29 days post infection at 9° C. No differences in development of lice, of either sex, were detected between the groups. As host groups were naive to sea lice at the start of the experiment, this suggests that there was a significant difference in susceptibility to sea lice infection between them, which may be genetically determined.

Notes: Biochemical genetic variation in populations of anadromous and resident brown trout, Salmo trutta L., was studied. Altogether 50 Norwegian populations were screened for 32 enzyme loci. Genetic polymorphism was found at the following 11 loci: AAT-4* (E.C. 2.6.1.1), CK-1* (E.C. 2.7.3.2), G3PDH-2* (E.C. 1.1.1.8), IDHP-2* (E.C. 1.1.1.42), LDH-5* (E.C. 1.1.1.27), MDH-2* (E.C. 1.1.1.37), MDH-3/4* (E.C. 1.1.1.37), MEP-2* (E.C. 1.1.1.40), GPI-2* (E.C. 5.3.1.9). GPI-5* (E.C. 5.3.1.9) and PGM-1* (E.C. 5.4.2.2), giving an overall polymorphism of 34%, ranging from 3.7 to 29.6% among individual populations. The average calculated heterozygosity ranged from 1.4 to 10.2% among populations. Genetic heterogeneity was observed among anadromous populations, and significant differences in allelic frequencies were found between anadromous populations in neighbouring watercourses, among resident populations and between anadromous and resident populations inhabiting the same watercourses. Significant heterogeneity was also found among 12 populations from Lake Mjøsa, with a major division between the western and eastern populations of the lake. Differences in allelic frequencies were found between wild stocks and their hatchery derivatives, and between different hatchery derivatives originating from the same wild population. In some cases release of hatchery populations into wild stocks may have influenced the genetic characteristics of wild stocks. The data support the hypothesis of eastern as well as western postglacial colonization lines for Norwegian brown trout.

Notes: Studies on genetic changes in farmed fish populations are reviewed, and the potential interactions between wild and farm escapee, and between wild and stocked, fish populations are discussed. Examples of the application of genetic markers in studies concerning survival and reproduction of stocked fish, and genetic and ecological interactions between stocks, are given for brook trout, Salvelinus fontinalis, brown trout, Salmo trutta, rainbow trout, Salmo gairdneri, cod, Gadus morhua, Guadalupe bass, Micropterus treculi, walleye, Stizostedion vitreum vitreum and chum salmon, Oncorhynchus keta. The various studies produced different results. Evidence for successful reproduction and genetic interactions between released and wild stocks have been found in a few cases. Stocked genetic material sometimes had a lower reproductive success than wild material. In one case the transplanted genetic material failed to acclimatize, and was apparently lost from the genepool in two generations. Investigations on the genetic and ecological interactions between wild and farmed populations are of great importance to the preservation of wild populations and their genetic resources.

Notes: In Lake Svartavasstjønn on the Hardangervidda plateau, a fine-spotted variant of brown trout has been found. The spotted variability shows a classical Mendelian mode of inheritance. In this population genetic variability was found in LDH-5*, MDH-3* and MDH-3*. The fast allele at LDH-5* had a frequency of 0,913. This is remarkable, as this allele has been found in frequencies above 0.4 in only five out of 50 investigated populations in Norway. The genetic characteristics of brown trout from Lake Svartavasstjønn were compared with 11 other populations sampled from a broad geographical area of Norway. Among these was Lake Setningen, where fine-spotted individuals occur at low frequency. Using a cluster analysis based on eight loci found to be polymorphic in brown trout, we found no indication of a close relationship between the fine-spotted brown trout from Lake Svartavasstjønn and the population in Lake Setningen. During a field survey in 1990 we found that the reproduction of fine-spotted trout in Lake Svartavasstjønn had terminated. The fine-spotted trout represents a valuable but threatened genetic resource, and attempts are carried out to conserve it.

Notes: Electrophoretic studies of proteins remain a primary source of insight into genetic diversity in many species including the Atlantic salmon Salmo salar, one of the most culturally and economically important fish species of the North Atlantic region. Since 1966, 〉350 scientific papers on protein variation have been published encompassing 25 000+ salmon from over 400 locations in 〉200 river systems across the species’ distribution. Variation has been detected at 30% of the 110 protein loci screened, though most studies examine 〈40. The method has been applied largely to the investigation of population structure and differentiation, but work has also led to the systematic revision of the genus Salmo and remains the primary source of insight into hybridization in the wild with brown trout Salmo trutta. Spatial patterns of differentiation show temporal stability, both within and among river systems, and strongly support structuring of the species into river and tributary specific populations and the designation of European and North American populations as distinct sub-species. They also show widespread regional differentiation within both continents, beyond the marked subcontinental differences between Baltic Sea and Atlantic Ocean populations in Europe. Most of the differentiation probably reflects gene flow and founder events associated with colonization following the retreat of the glaciers from much of the species’ modern range. However, variation at MEP-2* shows strong correlations with environmental temperature, both within and among rivers, and associations with phenotypic performance. This suggests selection is acting on the locus and provides compelling evidence for the local adaptation of populations. Protein studies have led to more population centred management of the species and have been exploited in the discrimination of regional stocks in mixed stock analysis in high seas fisheries, particularly in the Baltic Sea, and as markers for the assessment of stocking success. They have also advanced insight into how the genetic character of populations can be changed in cultivation and the potential impact of salmon aquaculture and stocking on wild populations. The method has been largely superseded by DNA based analyses, but the results remain highly relevant to Atlantic salmon management and conservation and are an irreplaceable data set for studying genetic stability of populations over time.

Notes: Distribution alleles of sAAT-1,2* isoloci in brown trout Salmo trutta populations of northern Europe revealed two glacial refugia, ‘Baltic’ and ‘Atlantic’.