Genetic differentiation of pink salmon oncorhynchus gorbuscha Walbaum in the Asian part of the range

Genetic variation at 19 allozyme (including 11 polymorphic) and 10 microsatellite loci was examined in the population samples of odd- and even-broodline pink salmon from the southern part of Sakhalin Island, Southern Kuril Islands, and the northern coast of the Sea of Okhotsk. The estimates of relative interpopulation component of genetic variation over the allozyme loci, per broodline, were on average 0.43% (GST), while over the microsatellite loci it was 0.26% (the theta(ST) coefficient, F-statistics based on the allele frequency variance), and 0.90% (the rho(ST) coefficient, R-statistics based on the allele size variance). The values of interlinear component constituted 2.34, 0.31, and 1.05% of the total variation, respectively. Using the allozyme loci, statistically significant intralinear heterogeneity was demonstrated among the regions, as well as among the populations of Southern Sakhalin Island. Multivariate scaling based on the allozyme data demonstrated regional clustering of the sample groups, representing certain populations during the spawning run or in different years. Most of the microsatellite loci examined were found to be highly polymorphic (mean heterozygosity > 0.880). The estimates of interlinear, interregional, and interpopulation variation over these loci in terms of theta(ST) values were substantially lower than in terms of rho(ST) values. Regional genetic differentiation, mostly expressed at the allozyme loci among the populations from the northern and southern parts of the Sea of Okhotsk (i.e., between the Sakhalin and Kuril populations), was less expressed at the microsatellite loci. The differentiation between these regions observed can be considered as the evidence in favor of a large-scale isolation by distance characterizing Asian pink salmon. It is suggested that in pink salmon, low genetic differentiation at neutral microsatellite loci can be explained by extremely high heterozygosity,of the loci themselves, as well as by the migration gene exchange among the populations (the estimate of the genetic migration coefficient inferred from the "private" allele data constituted 2.6 to 3.4%), specifically, by the ancient migration exchange, which occurred during postglacial colonization and colonization of the range.     

Genetic changes in pink salmon Oncorhynchus gorbuscha Walbaum during acclimatization in the White sea basin

Genetic parameters of pink salmon introduced into the White Sea basin in 1985 and 1998 were compared to the corresponding parameters of the donor population from the Ola River (Magadan oblast). The detected genetic differences indicate that colonization of a new area is accompanied by impoverishment of the gene pool of the native population. This effect was particularly marked in the odd-year line of pink salmon introduced in 1985. The probable causes of these genetic changes are discussed.     

Migration and capture of pink salmon, Oncorhynchus gorbuscha Walbaum in Finnmark, North Norway

Pink salmon transplanted to the north Atlantic coast from the Soviet Union reached a peak in 1973, both in the Soviet Union and in Finnmark. Pink salmon catch statistics were compiled in 1977 for the inshore coastal and fjord areas of Finnmark from the atlantic salmon fisheries conducted locally and outside the coastal limits of Finnmark. The survey indicated a total sea catch of 12 800 specimens or 18 450 kg in Finnmark in 1977. The pink salmon reached the coast in the western regions of Finnmark during the first half of July, after which the main migration continued eastwards along the coast. The migrations into the western fjords were few, with half the total inshore catch captured in the most eastern fjord, Varangerfjord.     

Genetic analysis of growth and maturity in pink salmon (Oncorhynchus gorbuscha)

Variation in growth and sexual maturity was examined for five stocks of pink salmon (Oncorhynchus gorbuscha) spawning at different times in British Columbia. In each stock, four males were mated with eight females in a nested breeding design, and the juveniles were reared for 500 d after fry emergence. Adults in early-spawning northern stocks were smaller than those in late-spawning southern ones, but pink salmon from northern stocks had faster growth rates than those from southern ones. The relative ranking within stocks of family weight remained constant after late winter in the year of maturity. Heritability of weight based upon sire variance components was usually greater than 0.9 after 150 d of rearing. Pink salmon from the earlier-spawning stocks were in a more advanced state of sexual maturity when the experiment was terminated than were those from later-spawning stocks, indicative of a significant genetic component in timing of sexual maturity.     

Changes in reproductive parameters during the spawning migration of pink salmon, Oncorhynchus gorbuscha (Walbaum)

The hormones 17β-estradiol, 17α-hydroxy-20β-dihydroprogesterone(17α, 20β-P), 11-ketotestosterone, testosterone, gonadotropin and also vitellogenin, were determined during the spawning migration of wild pink salmon in the Fraser and Thompson Rivers in British Columbia. This stock of pink salmon takes approximately 2 weeks to migrate the 333 km upstream to the spawning grounds. Both sexes were at an advanced stage of sexual development when they entered fresh water. In females both the 17β-estradiol and vitellogenin levels fell precipitously during the migration, to be very low at spawning, whereas the 17α,20β-P level rose rapidly, to be highest at arrival on the spawning grounds. The gonadotropin level also rose rapidly during the migration, and was highest in spent fish. Testosterone was at a high level throughout, although this level decreased steadily during migration. In many respects similar endocrine changes were observed in the male. For example, in the case of androgen levels, both testosterone and 11-ketotestosterone fell steadily during migration but were still relatively high at spawning, whereas both gonadotropin and 17α, 20β-P levels rose markedly as migration progress. However, although the qualitative changes were often similar between the sexes, the levels of 17α, 20β-P, testosterone, and gonadotropin were considerably higher throughout in females than in males. It is concluded that this stock of pink salmon is at an advanced stage of sexual development when it enters fresh water. The endocrine changes observed during this study represent those controlling the final stages of reproduction, specifically final oocyte maturation and ovulation in females, and the final stages of spermatogenesis and spermiation in males.     

Effect of hunger on the daily pattern of feeding rates in juvenile pink salmon, Oncorhynchus gorbuscha Walbaum

Juvenile pink salmon, Oncorhynchus gorbuscha , in two test groups of differing hunger level fed continuously on live copepods, maintained at high densities, throughout 12 h feeding periods in the laboratory. Analysis of video films showed that mean feeding rates were initially (first 10 min) between 51.5 and 63.8 prey-capture attempts (snaps) fish^-1 10 min^-1, but declined abruptly with increasing satiation to relatively constant levels of about 5.0 and 8.0 snaps fish^-1 10 min^-1, which were maintained during the subsequent 11 h of feeding. The data suggests that after the initial filling of their stomachs with food, juvenile pink salmon keep their stomachs full by feeding at a rate that balances the gastric evacuation rate of 18.6 mg prey h^-1 at 11° C. Less than 15% of the fish's stomach contents need be evacuated apparently for spontaneous feeding to resume or occur. Increased hunger level (by increasing a pre-test food deprivation period from 24 to 72 h) resulted in fish increasing their average feeding rate and thus their ration consumed from 23.6 to 39.8% dry body weight per 12 h.     

Dorsal hump morphology in pink salmon (Oncorhynchus gorbuscha)

Mature male Pacific salmon (Genus Oncorhynchus) develop a dorsal hump, as a secondary male sexual characteristic, during the spawning period. Previous gross anatomical studies have indicated that the dorsal humps of salmon are mainly composed of cartilaginous tissue (Davidson [1935] J Morphol 57:169–183.) However, the histological and biochemical characteristics of such humps are poorly understood. In this study, the detailed microstructures and components of the dorsal humps of pink salmon were analyzed using histochemical techniques and electrophoresis. In mature males, free interneural spines and neural spines were located in a line near to the median septum of the dorsal hump. No cartilaginous tissue was detected within the dorsal hump. Fibrous and mucous connective tissues were mainly found in three regions of the dorsal hump: i) the median septum, ii) the distal region, and iii) the crescent‐shaped region. Both the median septum and distal region consisted of connective tissue with a high water content, which contained elastic fibers and hyaluronic acid. It was also demonstrated that the lipid content of the dorsal hump connective tissue was markedly decreased in the mature males compared with the immature and maturing males. Although, the crescent‐shaped region of the hump consisted of connective tissue, it did not contain elastic fibers, hyaluronic acid, or lipids. In an ultrastructural examination, it was found that all of the connective tissues in the dorsal hump were composed of collagen fibers. Gel electrophoresis of collagen extracts from these tissues found that the collagen in the dorsal hump is composed of Type I collagen, as is the case in salmon skin. These results indicate that in male pink salmon the dorsal hump is formed as a result of an increase in the amount of connective tissue, rather than cartilage, and the growth of free interneural spines and neural spines. J. Morphol. 275:514–527, 2014. © 2013 Wiley Periodicals, Inc.     

Changes in the North Channel fish community,with emphasis on pink salmon (Oncorhynchus gorbuscha Walbaum)

Historical trends in commercial fishery yields were examined for evidence of structural changes in the North Channel fish community. Significant declines in the abundance of indigenous species occurred primarily as a result of man's activities. Lake sturgeon (Acipenser fulvescens Rafinesque) were harvested down to low levels by 1900. Introductions of exotics to the fish community were associated with major changes. Rainbow smelt (Osmerus mordax Mitchill) and sea lamprey (Petromyzon marinus Linnaeus) colonized the channel in the late 1930s. Concurrently, lake trout (Salvelinus namaycush Walbaum) and burbot (Lota lota Linnaeus), the top deepwater predators, declined to near extinction. Lake whitefish (Coregonus clupeaformis Mitchill) and shallow-water cisco (Coregonus artedii Lesueur) also declined. Without predation pressure, smelt abundance increased to high levels in the 1950s and alewife (Alosa pseudoharengus Wilson), another exotic, peaked during the 1960s. Both species equilibrated at lower levels in the 1970s, perhaps favouring colonization by pink salmon (Oncorhynchus gorbuscha Walbaum). Pink salmon which are larger and more fecund in Lake Huron than in Lake Superior, are increasing rapidly in numbers and are expanding their range in the channel. Certain whitefish stocks have increased sufficiently to support fishery yields greater than those of the 1930s, despite considerable exploitation pressure. This success is partially in response to the control of sea lamprey since 1961. However both lake whitefish and walleye (Stizostedion vitreum Mitchill) are now rare in the east end of the channel, possibly due to environmental factors such as acid precipitation and metal contaminants. Community stability will not likely be attained until a suitable climax predator becomes reestablished.     

Evidence of potential establishment of pink salmon Oncorhynchus gorbuscha in Scotland

In spring 2022, pink salmon Oncorhynchus gorbuscha smolts were recorded in the UK. Fish were caught in the Rivers Thurso and Oykel in Scotland between 13 and 17 March. To the authors’ knowledge, this is the first observation of O. gorbuscha smolts in Europe outside the Scandinavian and Kola peninsulas, including other tributaries of the White and Barents Seas. It also provides evidence of successful spawning in 2021 and completion of the freshwater phase of the life cycle, and indicates the possibility for potential establishment of an O. gorbuscha population in Great Britain.     

Heavy metal contents in the pink salmon Oncorhynchus gorbuscha Walbaum, 1792 from Kuril oceanic waters during anadromous migration

The contents of trace elements, viz., Hg, As, Pb, Cd, Zn, and Cu, in a common species of Pacific salmon, viz., the pink salmon, which were caught in early July 2012 and 2013 in the vicinity of Kuril Islands, were examined. It was found that the contents of toxic elements, Cd, Pb, As, and Hg, in the salmon meet human-health consumption guidelines for seafood by the sanitary standards and regulations of the Russian Federation. The contents of all of the metals (except zinc) in pink salmon from the geochemically extreme Kuril area were higher than that in pink salmon from the Sea of Japan. The greatest difference was recorded for lead, whose concentrations in organs and tissues (liver, gonads, and muscle) of fish from Kuril oceanic waters was one and a half order of magnitude higher than that of pink salmon from the Sea of Japan.     

Evidence of successful recruitment of non-native pink salmon Oncorhynchus gorbuscha in Iceland

In mid-May 2022, pink salmon Oncorhynchus gorbuscha smolts were caught in the rivers Botnsá, Grímsá, and Langá in Iceland. This observation provides the first evidence of successful spawning and the completion of the freshwater phase of the life cycle in Icelandic rivers. It is the most western record of O. gorbuscha smolts in Europe, further west than Russia, Norway, and the UK. Smolts originating from Iceland potentially support the recruitment of this species in the North Atlantic and may lead to the establishment of a self-sustaining population in Iceland.     

Genetic linkage mapping of allozyme loci in even- and odd-year pink salmon (Oncorhynchus gorbuscha)

We constructed genetic linkage maps of allozyme loci in even- and odd-year pink salmon (Oncorhynchus gorbuscha), using the total of 320 families (each female was crossed with two different males, and 80 females and 160 males were used for each of even year and odd year). The maps include eight linkage groups involving 22 loci. We observed substantial variation in recombination frequencies among different families within broodline and between sexes within broodlines. In the linkage analysis between sAAT-3* and sMDH-B1,2*, two even-year families and one odd-year family exhibited evidence of association, but two even-year and one odd-year families did not. Recombination rate tends to be reduced in males in pink salmon. The ratio of recombination rate (female/male), which ranged from 1.7 to infinity, averaged 2.8 in the even-year crosses and 3.2 in the odd-year crosses. The linkage groups (LG) I and II involving sAAT and mAH loci, which probably duplicated in the recent tetraploidization event, and the orders of loci in the LGs I (sAAT-3* --> mAH-4*) and II (mAH-3* --> sAAT-4*) were reversed, suggesting the possible paracentric inversion during salmonid evolution after the duplication.     

Genetic stock structure of odd-year pink salmon, Oncorhynchus gorbuscha (Walbaum), from Washington and British Columbia and potential mixed-stock fisheries applications

We used electrophoresis to determine the number and characteristics of genetically distinct stocks of odd-year pink salmon in Washington and southern British Columbia. We analysed 5128 fish from 52 collections (taken in 1985, 1987 and 1989). We observed genetic variation at 53 enzyme-coding loci, 19 of which were polymorphic at the P_o-95 level in at least one stock. Genotypic proportions conformed to Hardy-Weinberg expectations in nearly all cases. The genetic profiles of individual populations were generally stable over the three cycle years studied. Significant differences in allele frequencies at sAAT-3* , PEP-LT* and PGDH* for several stocks were, however, noted between this study and previously reported data for pink salmon. We used G-tests and cluster analysis of genetic distances to evaluate genetic interrelationships among collections and to define genetically distinct stocks. Differentiation among stocks exhibited a clear geographic pattern with three major clusters of stocks recognizable: (1) Hood Canal and Washington Strait of Juan de Fuca stocks, (2) Puget Sound, Fraser River, and southern Canada South Coast stocks, and (3) northern Canada South Coast stocks and Canada North Coast stocks. Computer simulations using 14 and 28 loci, and sample sizes of 15C600, demonstrated that accurate estimates of stock-group composition could be obtained for pink salmon fisheries having a considerable range of stock compositions. The simulations revealed that approximately 50% fewer fish were required to obtain a given level of precision of stock group composition estimates with 28 loci as with the set of 14 loci used in previous investigations.     

Behavior of juvenile pink salmon (Oncorhynchus gorbuscha Walbaum) toward novel prey: influence of ontogeny and experience

Synopsis The behavior of individual, juvenile pink salmon toward novel prey (Artemia salina) under laboratory conditions is described. Two aspects of predatory behavior, namely latency time to initial prey-capture attempt and prey-capture success, are quantified in relation to chronological age and feeding experience. Initially, mean latency time declined slightly with increasing age up to Day 19 (post-emergence from gravel), but increased sharply to an asymptote with further aging. Mean percentage capture success gradually increased from 7.88% on Day 1 to 92.9% on Day 45. Prior feeding experience on the prey resulted in a decline (to a stable level) in mean latency time in experienced fish compared to control fish. Mean percentage capture success was not significantly altered by prior feeding experience on the prey.     

Allozyme heterozygosity and morphological homeostasis in pink salmon,Oncorhynchus gorbuscha (Walbaum): evidences from family analysis*

In the families produced by diallel 2 × 2 crosses there were positive relationships in two experimental groups between individual heterozygosity (H₀) at four allozyme loci (PGM*, G3PDH*, sMEP*, sMDH?3,4*) and the size of the fish, their morphological variability (10 traits) and the viability among families. An integrative H₀ influence on complexes of morphological traits was also obtained. On the basis of factor and discriminant analysis it was shown that H₀ correlated with morphological homeostasis at least within one experimental group.     

A genetic analysis of body size in pink salmon (Oncorhynchus gorbuscha)

Two small-sized and two large-sized male pink salmon (Oncorhynchus gorbuscha) were mated to each of four females, producing eight families sired by small males and eight sired by large males. The juveniles were reared for 500 d after fry emergence. Juvenile weight in the two male size classes was similar until the spring of the year of maturity, when juveniles sired by large males grew faster than those sired by small ones. Heritability estimates of weight based upon the dam component of variance increased during 500 d of rearing from 0.4 to 0.8. Heritability of weight based upon the sire component of variance generally ranged between 0.1 and 0.3. The large variation in male body size in spawning pink salmon populations may have resulted from different male breeding strategies.     

Identification of the sex chromosome pair in chum salmon (Oncorhynchus keta) and pink salmon (Oncorhynchus gorbuscha)

Fluorescence in situ hybridization (FISH) using a probe to the male-specific GH-Y (growth hormone pseudogene) was used to identify the Y chromosome in the karyotypes of chum salmon (Oncorhynchus keta) and pink salmon (Oncorhynchus gorbuscha). The sex chromosome pair is a small acrocentric chromosome pair in chum salmon and the smallest metacentric chromosome pair in pink salmon. Both of these chromosome pairs are morphologically different from the sex chromosome pairs in chinook salmon (Oncorhynchus tshawytscha) and coho salmon (Oncorhynchus kisutch). The 5S rRNA genes are on multiple chromosome pairs including the sex chromosome pair in chum salmon, but at the centromeres of two autosomal metacentric pairs in pink salmon. The sex chromosome pairs and the chromosomal locations of the 5S rDNA appear to be different in all five of the North American Pacific salmon species and rainbow trout. The implications of these results for evolution of sex chromosomes in salmonids are discussed.