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Investigations of genetic stock structure sometimes reveal a mismatch between management units and biological units. In Scandinavian waters, Norway lobster (Nephrops norvegicus) is divided into two management units (the Skagerrak–Kattegat and the Norwegian Deep). We have tested the population genetic structure of Nephrops within this region using microsatellite DNA markers, and compared the structure with the present management units. Our study suggests no population genetic structure of Nephrops within the Skagerrak, Kattegat, and Norwegian Deep region, whereas a shallow genetic structure was detected on a larger geographical scale when comparing outgroup samples from Scotland and Iceland. We found indications of sex-biased dispersal as the overall genetic differences were larger for females. Ocean current patterns suggest that Nephrops stocks in the region may be connected by larval drift. The two areas differ in fishing pressure, monitoring, assessment, and regulations, which is an argument for maintaining the present two-areas management regime despite the evidence for one biological population.

Environmental DNA (eDNA) has gained popularity as a tool for ecosystem biomonitoring and biodiversity assessment. Although much progress has been made regarding laboratory and fieldwork protocols, the issue of sampling efficiency requires further investigation, particularly in three-dimensional marine systems. This study focuses on fish community composition in marine ecosystems and aims to analyze the efficiency of sampling design given the sampling effort for distinguishing between different communities. We sampled three fjords in Northern Norway, taking samples along fjord transects and at three different depths, and amplified a fragment of the mitochondrial 12S rRNA gene of bony fishes using the MiFish primers. We evaluated the effect of (i) the number of sampling stations, (ii) samples' spatial distribution, and (iii) the data treatment approach (presence/absence versus semiquantitative) for maximizing the efficiency of eDNA metabarcoding sampling when inferring differences of fish community compositions between fjords. We found that the manner of data treatment strongly affected the minimum number of sampling stations required to detect differences among communities; because the semiquantitative approach retained some information about abundance of the underlying reads, it was the most efficient. Furthermore, we found little-to-no difference of fish communities in samples from intermediate depths when comparing vertical fish communities. Lastly, we found that the differences between fish communities at the surface were the highest across the horizontal distance and overall, samples ~30 km apart showed the highest variation in the horizontal distribution. Boosting sampling efficiency (reducing sampling effort without compromising ecological inferences) can significantly contribute to enhanced biodiversity management and efficient biomonitoring plans.

The snow crab (Chionoecetes opilio) is an Arctic cold-water species native to the northwestern Atlantic Ocean and the northern Pacific Ocean. During the recent decades, a population has established in the Barents Sea. Several aspects of the snow crabs’ biology in this area have not been described, including time of hatching, intermoult duration of the different larval stages and larval distribution. Insight into the early-life stages might increase the understanding of the population's dynamics and further spreading in the Barents Sea as well as inform basis for making monitoring and management decisions. The present study investigated the presence and developmental stage of snow crab larva in plankton samples obtained in the central Barents Sea during a research survey in June and July 2019. Presence of snow crab larvae was confirmed through taxonomic and genetic identification. All larvae were identified as zoea I, which gives an indication of the timing of the hatching period. Morphological measurements coincide well with those reported in studies from the species native distribution range. No larvae of native Hyas spp. were found and overlap in temporal and spatial distribution is discussed. The study provides important information for development of further research into the biology of the snow crab in the Barents Sea.

Many marine organisms have a permanent presence both inshore and offshore and spawn in multiple areas, yet their status as separate populations or stocks remain unclear. This is the situation for the northern shrimp (Pandalus borealis) around the Arctic Ocean, which in northern Norway represents an important income for a small-scale coastal fishery and a large-vessel offshore fleet. In Norwegian waters, we uncovered two distinct genetic clusters, viz. a Norwegian coastal and a Barents Sea cluster. Shrimps with a mixed heritage from the Norwegian coastal and the Barents Sea clusters, and genetically different from both, inhabit the fjords at the northernmost coast (Finnmark). Genetic structure between fjords did not display any general trend, and only the Varangerfjord in eastern Finnmark displayed significant genetic structure within the fjord. Shrimps in the Finnmark fjords differed in some degree from shrimps both in the adjacent Barents Sea and along the rest of the coast and should probably be considered a separate management unit.

The advent of novel genetic methods has made it possible to investigate population structure and connectivity in mobile marine fish species: knowledge of which is essential to ensure a sustainable fishery. Haddock (Melanogrammus aeglefinus) is a highly exploited marine teleost distributed along the coast and continental shelf on both sides of the North Atlantic Ocean. However, little is known about its population structure. Here, we present the first study using single-nucleotide polymorphism (SNP) markers to assess the genetic population structure of haddock at multiple geographic scales, from the trans-Atlantic to the local (fjord) level. Genotyping 138 SNP loci in 1329 individuals from 19 locations across the North Atlantic revealed three main genetic clusters, consisting of a Northwest Atlantic cluster, a Northeast Arctic cluster, and a Northeast Atlantic cluster. We also observed a genetically distinct fjord population and a pattern of isolation by distance in the Northeast Atlantic. Our results contrast with the current management regime for this species in the Northeast Atlantic, as we found structure within some management areas. The study adds to the growing recognition of population structuring in marine organisms in general, and fishes in particular, and is of clear relevance for the management of haddock in the Northeast Atlantic.

Challenging long‐held perceptions of fish management units can help to protect vulnerable stocks. When a fishery consisting of multiple genetic stocks is managed as a single unit, overexploitation and depletion of minor genetic units can occur. Atlantic cod (Gadus morhua) is an economically and ecologically important marine species across the North Atlantic. The application of new genomic resources, including SNP arrays, allows us to detect and explore novel structure within specific cod management units. In Norwegian waters, coastal cod (i.e. those not undertaking extensive migrations) are divided into two arbitrary management units defined by ICES: one between 62° and 70°N (Norwegian coastal cod; NCC) and one between 58° and 62°N (Norwegian coastal south; NCS). Together, these capture a fishery area of >25,000 km2 containing many spawning grounds. To assess whether these geographic units correctly represent genetic stocks, we analysed spawning cod of NCC and NCS for more than 8,000 SNPs along with samples of Russian White Sea cod, north‐east Arctic cod (NEAC: the largest Atlantic stock), and outgroup samples representing the Irish and Faroe Sea's. Our analyses revealed large differences in spatial patterns of genetic differentiation across the genome and revealed a complex biological structure within NCC and NCS. Haplotype maps from four chromosome sets show regional specific SNP indicating a complex genetic structure. The current management plan dividing the coastal cod into only two management units does not accurately reflect the genetic units and needs to be revised. Coastal cod in Norway, while highly heterogenous, is also genetically distinct from neighbouring stocks in the north (NEAC), west (Faroe Island) and the south. The White Sea cod are highly divergent from other cod, possibly yielding support to the earlier notion of subspecies rank. publishedVersion

Background Atlantic cod (Gadus morhua L.) has formed the basis of many economically significant fisheries in the North Atlantic, and is one of the best studied marine fishes, but a legacy of overexploitation has depleted populations and collapsed fisheries in several regions. Previous studies have identified considerable population genetic structure for Atlantic cod. However, within Norway, which is the country with the largest remaining catch in the Atlantic, the population genetic structure of coastal cod (NCC) along the entire coastline has not yet been investigated. We sampled > 4000 cod from 55 spawning sites. All fish were genotyped with 6 microsatellite markers and Pan I (Dataset 1). A sub-set of the samples (1295 fish from 17 locations) were also genotyped with an additional 9 microsatellites (Dataset 2). Otoliths were read in order to exclude North East Arctic Cod (NEAC) from the analyses, as and where appropriate. Results We found no difference in genetic diversity, measured as number of alleles, allelic richness, heterozygosity nor effective population sizes, in the north-south gradient. In both data sets, weak but significant population genetic structure was revealed (Dataset 1: global FST = 0.008, P

Exploited marine resources can be managed more effectively when accurate information on geographic population structure is available. Genetic markers offer a powerful tool for fisheries management, because they reveal biologically sound management units. Single nucleotide polymorphisms (SNPs) markers derived from restriction-site associated DNA sequencing (RAD-seq) were developed and used to investigate the stock structure of Greenland halibut (Reinhardtius hippoglossoides). A total of 96 SNPs were analyzed from 384 individuals and eight locations across the Atlantic. Our results suggest a subdivision of Greenland halibut into two populations, an eastern Atlantic population and a western Atlantic population, with a proposed border across the Denmark Strait. In general, Greenland halibut display weak but significant population structure (overall FST= 0.003; p < 0.001), which can be explained by connectivity among populations owing to the migratory behavior or egg and larval drift.

Published version, available at: https://doi.org/10.1038/s41598-019-42097-x As a result of ocean warming, the species composition of the Arctic seas has begun to shift in a boreal direction. one ecosystem prone to fauna shifts is the Northeast Greenland shelf. the dispersal route taken by boreal fauna to this area is, however, not known. This knowledge is essential to predict to what extent boreal biota will colonise Arctic habitats. Using population genetics, we show that Atlantic cod (Gadus morhua), beaked redfish (Sebastes mentella), and deep-sea shrimp (Pandalus borealis) recently found on the Northeast Greenland shelf originate from the Barents Sea, and suggest that pelagic offspring were dispersed via advection across the Fram Strait. Our results indicate that boreal invasions of Arctic habitats can be driven by advection, and that the fauna of the Barents Sea can project into adjacent habitats with the potential to colonise putatively isolated Arctic ecosystems such as Northeast Greenland.

Fish stocks represent fundamental units in fisheries management, and their identification, especially in mixed-fisheries, represents one of the primary challenges to sustainable harvest. Here, we describe the first “real-time” genetic management program used to manage a mixed-stock fishery of a non-salmonid and commercially significant marine fish, the Atlantic cod (Gadus morhua L). Based upon the analysis of >18 000 fish sampled from the commercial catch in Lofoten (Norway), which represents the largest remaining cod fishery in the Atlantic, we estimated the fraction of North East Arctic cod (NEAC), and Norwegian Coastal cod (NCC), just 24 h post-landing. These estimates, based upon the analysis of the Pantophysin gene, were performed weekly in the winter and spring of each year in the period 2007–2017. The program has successfully permitted the Norwegian Directorate of Fisheries to actively manage the commercial exploitation of the highly abundant NEAC stock, while simultaneously limiting exploitation of the fragile NCC stock, both of which overlap at the spawning grounds. Data from this program have also revealed a distinct temporal increase in the fraction of NEAC on the spawning grounds in this region, which is consistent with the overall increased abundance of this stock as estimated by ICES. publishedVersion

Published version. Source at http://doi.org/10.3354/sedao00013. Large offshore and small inshore populations of Atlantic cod Gadus morhua L. display differences in migratory patterns and settling regimes, but little is known about possible differences in spawning behaviour. Cod presumably of the Norwegian coastal cod type were therefore sampled during 7 spawning seasons (2002-2013) in Malangen, northern Norway. A spawning site in neighbouring Balsfjord was sampled during 5 consecutive spawning seasons (2002-2006). Length, weight, sex and maturity stage were recorded for each individual fish (n = 995). To verify their population assignment, frequencies of the 2 different Pan I (pantophysin) alleles were measured in 6 sampling years in Malangen and 3 in Balsfjord (n = 728). During all survey years there was an extreme skewed sex ratio at the spawning sites. In 6 of 7 seasons in Malangen, 8–9 of 10 fish were males, and in Balsfjord 9 of 10 fish were males on average, indicating some form of lekking behaviour among the spawning fish. Average size of the fish varied among years and also between sexes in individual years, although not consistently. The smallest proportion of mature fish was seen in Malangen in the year with the earliest sampling date (23 February). This was also the sample with the least skewed sex ratio (6.5 of 10 fish were males). The frequency of the Pan IA allele of the Malangen cod was highly stable among years at close to 90%, showing that this spawning ground is exclusively used by coastal cod. In Balsfjord, frequencies of the Pan IA allele were lower (67-78%). This fjord is suggested to be more penetrable for the migratory NE Arctic cod with their high frequencies of the Pan IB allele, making it a less exclusively coastal cod residence. In both fjords, length of mature males but not females varied among the Pan I genotypes.

WOS:000404450700007; Recently, there have been reports of increased abundance and landings of European hake in the northern part of the species range. Biological studies are however scarce and information about finer scale population structure important for stock assessments and fishery management is largely lacking. Here, we report on a population genetic study using neutral and outlier SNP loci assessing population structure in hake in the north-eastern parts of its range in the Atlantic. Hake samples from localities along the west coast of Norway, the Kattegat, the northern North Sea, and one locality in the Bay of Biscay were analysed using 53 SNPs, six of which were outliers potentially influenced by natural selection. We detected small-scale structure among northern samples, all of which were also distinct from Bay of Biscay hake, with the exception of a few individuals from the North Sea and the coast of Norway who clustered genetically together with Bay of Biscay hake. Our findings suggest that the present management unit of a single northern stock of hake is not biologically correct, and that there is more detail in the fine-scale population structure indicating that independent population dynamics could be expected in response to fishing patterns or changing environmental conditions.

Genetic population structure is often used to identify management units in exploited species, but the extent of genetic differentiation may be inflated by geographic variation in the level of hybridization between species. We identify the genetic population structure of Sebastes mentella and investigate possible introgression within the genus by analyzing 13 microsatellites in 2562 redfish specimens sampled throughout the North Atlantic. The data support an historical divergence between the ‘shallow’ and ‘deep’ groups, beyond the Irminger Sea where they were described previously. A third group, ‘slope’, has an extended distribution on the East Greenland Shelf, in addition to earlier findings on the Icelandic Slope. Furthermore, S. mentella from the Northeast Arctic and Northwest Atlantic waters are genetically different populations. In both areas, interspecific introgression may influence allele frequency differences among populations. Evidence of introgression was found for almost all the identified Sebastes gene pools, but to a much lower extent than suggested earlier. Greenland waters appear to be a sympatric zone for many of the genetically independent Sebastes groups. This study illustrates that the identified groups maintain their genetic integrity in this region despite introgression. This article is protected by copyright. All rights reserved.

With the decline of many of the world’s fisheries, increased regulation, including marine protected areas (MPA), forms an increasingly important role in promoting sustainable resource use. Here, we present a novel “real-time” genetic monitoring programme used to protect the depleted Norwegian coastal cod stock (NCC) in an MPA during the spawning season, while a fishery targeted at the sustainable Northeast Arctic cod stock (NEAC) operates immediately outside. In the period 2009–2016, >6800 cod from the fishery were genotyped with the PanI locus that is discriminatory between these two stocks. The estimated fraction of NEAC increased during the study period until 2014; however, it did not exceed 70% for any sustained period. Therefore, the MPA remained closed for commercial harvest. Genetic analysis of eggs revealed a distinctly lower fraction of NEAC than in the catch from the adult stock, both immediately outside and within the MPA itself. We suggest that this discrepancy is likely to reflect differences in spawning areas used by NCC and NEAC. Estimated fractions of NEAC/NCC using PanI, otolith classification, and 39 single nucleotide polymorphisms were similar, thus validating the use of PanI to estimate NEAC/NCC composition.

Genetic population structure is often used to identify management units in exploited species, but the extent of genetic differentiation may be inflated by geographic variation in the level of hybridization between species. We identify the genetic population structure of Sebastes mentella and investigate possible introgression within the genus by analyzing 13 microsatellites in 2,562 redfish specimens sampled throughout the North Atlantic. The data support an historical divergence between the “shallow” and “deep” groups, beyond the Irminger Sea where they were described previously. A third group, “slope,” has an extended distribution on the East Greenland Shelf, in addition to earlier findings on the Icelandic slope. Furthermore, S. mentella from the Northeast Arctic and Northwest Atlantic waters are genetically different populations. In both areas, interspecific introgression may influence allele frequency differences among populations. Evidence of introgression was found for almost all the identified Sebastes gene pools, but to a much lower extent than suggested earlier. Greenland waters appear to be a sympatric zone for many of the genetically independent Sebastes groups. This study illustrates that the identified groups maintain their genetic integrity in this region despite introgression.

We developed and characterized 20 microsatellite primer loci for the northern shrimp Pandalusborealis. All 20 loci were polymorphic with number of alleles ranging from 3 to 36 and with observed heterozygosity between 0.04 and 0.93. In addition, we tested the utility of these markers in three related shrimp species, P. montagui, Atlantopandaluspropinqvus and Dichelopandalusbonnieri. These new markers will prove useful in the identification of stock structure and hence, assessment of the commercially important species P. borealis.

Summary This study presents a molecular genetic characterization of Atlantic cod reared in commercial marine farms. Samples consisted of approximately 47 fish collected from nine cages located on four farms throughout Norway. In addition, 28 farmed escapees were recaptured in the sea (443 fish in total). Nine microsatellite loci and the Pan I gene were analysed, revealing a total of 181 alleles. Each sample contained 43‐63% of total allelic variation. Comparing variation with published data for wild cod indicates that lower genetic variation exists within single cages than in wild populations. Significant linkage disequilibrium was observed amongst pairs of loci in all samples, suggesting a low number of contributing parental fish. Global FST was 0.049, and the highest pairwise FST value (pooled loci) was 0.085. For single loci, the Pan I gene was the most diagnostic, displaying a global FST of 0.203. Simulations amongst the samples collected on farms revealed an overall correct self-assignment percentage of 75%, demonstrating a high probability of identifying individuals to their farm of origin. Identification of the 28 escapees revealed a single cage as the most likely source of origin for half of the escapees, whilst the remaining fish were assigned to a mixture of samples, suggesting more than one source of escapees.

A first genetic linkage map of the Atlantic cod (Gadus morhua) was produced, based on segregation data from 12 full-sib families of Norwegian origin. The map contained 174 single nucleotide polymorphism markers and 33 microsatellites, distributed on 25 linkage groups and had a length of 1225 cM. A significant difference in recombination rates between sexes was found, the average ratio of female:male recombination rates being 1.78 +/- 1.62 (SD).

Capelin Mallotus villosus is the most abundant pelagic fish species in boreal and sub- arctic waters. The ecological and commercial importance of capelin emphasizes the need for a better understanding of the genetic population structure of the species and the mechanisms underlying its population dynamics. With this aim, 1155 capelin from the entire distributional range of the species were genotyped using 9 recently-developed microsatellite markers. The genetic analyses clearly demonstrated that the circumpolar capelin population can be divided into 4 regional groups: (1) West Pacific, (2) East Pacific, (3) Newfoundland, and (4) Northeast Atlantic and West Greenland. Highly significant genetic differentiation was observed between capelin from the western and eastern Pacific, and a high assignment success within both regions indicated minimal gene flow between these populations. Within the Atlantic Ocean, the Newfoundland population was differentiated from all the other samples. Among the remaining samples within the Atlantic Ocean the microsatellite data were less conclusive. Comparison of our results with studies of species with similar distribution, duration of planktonic stages and dispersal capacity suggests that genetic structuring of capelin within the complex system of the Northeast Atlantic Ocean cannot be ruled out.

A large majority of Atlantic cod (Gadus morhua) found all year round in outer parts of fjords and along outer coastal areas in general in northern Norway have a genetic signature at the pantophysin (Pan I) locus that distinguish them from Norwegian coastal cod (NCC) found further inside fjords in the same areas. The identity of these fish has been controversial and to examine if they represent a distinct coastal cod group, or are identical to the migratory North East Arctic cod (NEAC) of the Barents Sea, a comparison was conducted at 10 microsatellite loci for 15 samples comprising each of the three groups inner coastal NCC, outer coastal cod and NEAC. Spatial analysis of molecular variance revealed that the outer coastal samples cannot be discriminated from NEAC by means of microsatellite markers, supporting the similarity of the two groups at the Pan I locus. This implies that a portion of the otherwise migratory NEAC, at least in its premature stage, remains in coastal areas in close contact with the genetically quite distinct NCC group. Both the coalescent-based simulation approach and the lnRH test for selective sweeps proved two of the microsatellite loci, GMO 34 and GMO 132 to be non-neutral. Notwithstanding, these two loci, together with the acknowledged non-neutral Pan I locus, which displayed profound linkage disequilibrium to GMO 34 within NEAC, are as yet the only nuclear markers which unambiguously discriminate between NEAC and NCC. Although the relative contribution of restricted gene flow versus selection as a causative agent for the divergence between NEAC and NCC has not been assessed, we believe the magnitude of differentiation at the three loci provides rational for maintaining NEAC and NCC as separate management units.

Although the actiology of swimbladder inflation anomalies in important aquaculture species such as European sea bass D. labrax is not fully determined, culture conditions are commonly suggested as main contributory factors. Little information is available on whether swimbladder inflation has a genetic basis for its expression too. In this work, 24 full-sibling sea bass families from a 4 dams x 6 sires factorial crossing were reared under communal conditions. The larvae developing normal and abnormal (uninflated or hyper-inflated) swimbladders were genotyped at four microsatellite loci, Labrax-3, Labrax-13, Labrax-17, Labrax29, and allocated to the individual breeders. Out of 273 offspring, 97% could be assigned to a single parental pair. The genotype and pedigree analysis showed an imbalance in family size due to differential survival of larvae with normally inflated swimbladders, with the offspring generated from one dam and one sire being two- to three-fold superior to the other parents, respectively. In larvae with non-inflated swimbladder, significant differences in family size were observed only among half-sibling sire families, whereas in larvae with hyper-inflated swimbladder such differences were found both among half-sibling sire and dam families. The results suggest that paternally and maternally inherited factors may contribute to the expression of swimbladder anomalies in sea bass along with major environmental clues. (c) 2007 Published by Elsevier B.V.

Ten polymorphic microsatellite markers were developed from approximately 1,300 expressed sequence tags (ESTs) of Atlantic cod (Gadus morhua L.). Thirty two primer pairs were designed for EST sequences containing perfect di- tri- tetra- and pentanucleotide motifs and characterised in 96 unrelated fish. Ten markers were successfully amplified with number of alleles from 2 to 13 per locus and observed and expected heterozygosity ranging from 0.03 to 0.69 and 0.03 to 0.74, respectively. Loci Gmo-C131, C132 and C136 deviated from Hardy-Weinberg equilibrium. Genetic linkage disequilibrium analysis between all pairs of the loci showed significant departure from the null hypothesis between loci Gmo-C131 and Gmo-C132 and C128 and Gmo-C133. The gene identity was determined at five of the loci, confirming the associated microsatellites as Type I markers. The new microsatellites reported in this work can be used for conservation and enhancement of wild stocks for commercial harvesting.

The large-scale population genetic structure of northern shrimp, Pandalus borealis, was investigated over the species’ range in the North Atlantic, identifying multiple genetically distinct groups. Genetic divergence among sample localities varied among 10 microsatellite loci (range: FST = −0.0002 to 0.0475) with a highly significant average (FST = 0.0149; P

Significant genetic differences (FST = 0·032) were found between littoral and profundal morphs of Arctic charr Salvelinus alpinus from Fjellfrosvatn, northern Norway, using microsatellite DNA analysis. The morphs had strong reproductive isolation in time and space; the segregation of a separate profundal morph is rare in postglacial lakes.

A novel hexaplex assay system including Gmo8, Gmo19, Gmo35, Gmo37, Tch11, and Tch12 microsatellites from Atlantic cod, consisting of trinucleotide or tetranucleotide repeat units, is introduced. All 6 loci were coamplified in a single reaction employing dye-labeled primers. Alleles from these loci were sized using an internal standard by automated sample processing in an ABI 310 Genetic Analyser. Amplified alleles in profiles containing selected microsatellites were typed clearly, providing easily interpretable results. Sequencing data indicated that alleles at all loci consisted of simple repeat units. This may help minimize the likelihood of stuttering upon polymerase chain reaction amplification. The results suggest that the presented hexaplex assay system may be a useful tool in a selective breeding program in which genetic identification will allow different genotypes to be reared together from fertilization. This should have a great impact as it will make selective breeding more efficient.

Fourteen polymorphic microsatellite markers with tetranucleotide repeats were developed for the bearded goby (Sufflogobius bibarbatus) from partial genomic DNA libraries using a repeat enrichment protocol, and characterized using two putative populations from the northern Benguela. The average number of alleles per locus ranged from 4 to 34, and the observed heterozygosities across loci were between 0.237 and 0.983. We also tested the utility of these markers in two other marine gobies; sand goby Pomatoschistus minutus and two-spotted goby Gobiusculus flavescens. These polymorphic markers can be employed to investigate population structure and related questions of the bearded goby.

A total of 13 polymorphic microsatellite markers were developed for Atlantic cod (Gadus morhua L.) from a repeat-enriched library. Polymorphism of each locus was assessed in 96 unrelated individuals from a natural population. The number of alleles per locus varied from 8 to 45. The ranges of observed and expected heterozygosity were 0.122–0.907 and 0.673–0.965, respectively. Four of the loci (Gmo-G24, Gmo-G40, Gmo-G46 and Gmo-G49) followed Hardy–Weinberg expectation. No evidence for linkage disequilibrium between pairs of loci was found in any combination of loci pairs, except between Gmo-G40 and Gmo-G43. These microsatellite markers provide useful tools for studies of population genetics, reproductive ecology and for constructing linkage maps of Atlantic cod.

We sampled 0-group juvenile Atlantic cod Gadus morhua L. within fjords and off- shore in northern Norway from 1994 to 2008 using different gears for the 3 sampling depths: shore seine (0�3 m), pelagic trawl (various depths), and bottom trawl (>80 m). Frequencies of alleles at the Pan I locus (4218 fish analysed) showed highly significant differences among samples col- lected in the different habitats. The Pan I A allele showed a mean frequency of ~80% in the shore seine samples, 12% in the bottom trawl samples, and between 5 and 57% in the pelagic samples. These differences are thought to reflect the co-occurrence of different populations of cod in the area with different settling regimes. Shallow-water settlers are thought to represent the stationary Norwegian coastal cod (NCC), the deep-water settlers represent the migratory Arcto-Norwegian cod (ANC), and the non-settled individuals represent a variable mixture of the 2 populations. For designated samples, we analyzed 16 microsatellites (non-neutral and neutral) that supported a genetic divergence between shallow-water and deep-water settlers. Correlations between length and Pan I genotypes within selected samples showed that the Pan I BB homozygotes (typical of ANC) were significantly longer than the Pan I AA homozygotes (typical of NCC). This could reflect differences in spawning time and growth conditions between ANC and NCC, just as well as one genotype being superior to the others in terms of growth performance. Finally, we argue that the Pan I difference between 0-group NCC and ANC is not caused by contemporary selection but reflects adaptation on an ecological post-glacial time scale.