From 25 July to II September 1984 Atlantic salmon, Salmo salar L-, parr were observed underwater between 0800 and 1600 h, feeding actively from defended territories at two sites in the River Tilt, Perthshire, Scotland. Territories comprised one or more preferred stations on or just above the substrate, from which the fish intercepted drifting particles (75% of feeding), or foraged on the substrate (25%). Drift feeding occurred 36% at the surface. 35% in mid-water and the remainder at the feeding station. 35% of prey particles were attacked directly from the feeding station, and 65% indirectly after preliminary inspection, sometimes involving a drift downstream by the fish. 20% of captures were made upstream of the station and 80% downstream. 12-15-cm fish fed more frequently at the surface, while lO-cm fish fed in mid-water or at their stations. Surface feeding decreased proportionately during rainfall. Frequency of feeding increased with temperature. Feeding was depressed in the presence of large saimo nids.

Microsatellite genotyping is a common DNA characterization technique in population, ecological and evolutionary genetics research. Since different alleles are sized relative to internal size-standards, different laboratories must calibrate and standardize allelic designations when exchanging data. This interchange of microsatellite data can often prove problematic. Here, 16 microsatellite loci were calibrated and standardized for the Atlantic salmon, Salmo salar, across 12 laboratories. Although inconsistencies were observed, particularly due to differences between migration of DNA fragments and actual allelic size (‘size shifts’), inter-laboratory calibration was successful. Standardization also allowed an assessment of the degree and partitioning of genotyping error. Notably, the global allelic error rate was reduced from 0.05 ± 0.01 prior to calibration to 0.01 ± 0.002 post-calibration. Most errors were found to occur during analysis (i.e. when size-calling alleles; the mean proportion of all errors that were analytical errors across loci was 0.58 after calibration). No evidence was found of an association between the degree of error and allelic size range of a locus, number of alleles, nor repeat type, nor was there evidence that genotyping errors were more prevalent when a laboratory analyzed samples outside of the usual geographic area they encounter. The microsatellite calibration between laboratories presented here will be especially important for genetic assignment of marine-caught Atlantic salmon, enabling analysis of marine mortality, a major factor in the observed declines of this highly valued species.Electronic supplementary materialThe online version of this article (doi:10.1007/s10709-011-9554-4) contains supplementary material, which is available to authorized users.

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Examination of the genetic basis of the timing of the return migration of Atlantic salmon (Salmo salar) to fresh water from the sea, a trait of economic and conservation interest, was carried out using a genome-wide association study. We examined genotype data of 52 731 single nucleotide polymorphic (SNP) markers from 73 early and 49 late running two-sea-winter salmon from five rivers in eastern Scotland. A single region of the Atlantic salmon chromosome Ssa09 was identified, containing nine SNP markers significantly associated with run timing, a region previously linked to variation in sea age at maturity. Validation of the markers in a group of 233 one- and two-sea-winter fish, including adults from a novel river, again showed significant associations between the trait and the Ssa09 region, explaining ∼24% of the trait variance. The SNP loci identified provide the ability to examine trait variation in populations of Atlantic salmon and so help facilitate conservation management of the differing run timing phenotypes.

Understanding the habitat use patterns of migratory fish, such as Atlantic salmon (Salmo salar L.), and the natural and anthropogenic impacts on them, is aided by the ability to identify individuals to their stock of origin. Presented here are the results of an analysis of informative single nucleotide polymorphic (SNP) markers for detecting genetic structuring in Atlantic salmon in Scotland and NE England and their ability to allow accurate genetic stock identification. 3,787 fish from 147 sites covering 27 rivers were screened at 5,568 SNP markers. In order to identify a cost-effective subset of SNPs, they were ranked according to their ability to differentiate between fish from different rivers. A panel of 288 SNPs was used to examine both individual assignments and mixed stock fisheries and eighteen assignment units were defined. The results improved greatly on previously available methods and, for the first time, fish caught in the marine environment can be confidently assigned to geographically coherent units within Scotland and NE England, including individual rivers. As such, this SNP panel has the potential to aid understanding of the various influences acting upon Atlantic salmon on their marine migrations, be they natural environmental variations and/or anthropogenic impacts, such as mixed stock fisheries and interactions with marine power generation installations.