Challenges for Diadromous Fishes in a Dynamic Global Environment

2009 ◽  
Keyword(s):  
Chinook Salmon ◽  
Large Scale ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Commercial Catch ◽  
Atmospheric Processes ◽  
Energy Transfers ◽  
Salmon Production ◽  
The Impact

<em>Abstract</em>.-Pacific salmon <em>Oncorhynchus </em>spp. catches are at historic high levels. It is significant that one of the world's major fisheries for a group of species that dominates the surface waters of the subarctic Pacific is actually very healthy. Natural trends in climate are now recognized to cause large fluctuations in Pacific salmon production, as shown in historical records of catch and recent changes probably have been affected by greenhouse gas induced climate changes. Pink salmon <em>O. gorbuscha </em>and chum salmon <em>O. keta </em>production and catch has increased in the past 30 years and may continue in a similar trend for for the next few decades. Coho salmon <em>O. kisutch </em>and Chinook salmon <em>O. tshawytscha </em>catches have been declining for several decades, particularly at the southern end of their range, and they may continue to decline. In the 1970s, hatcheries were considered to be a method of adding to the wild production of coho and Chinook salmon because the ocean capacity to produce these species was assumed to be underutilized. Large-scale changes in Pacific salmon abundances are linked to changes in large-scale atmospheric processes. These large-scale atmospheric processes are also linked to planetary energy transfers, and there is a decadal scale pattern to these relationships. Pacific salmon production in general is higher in decades of intense Aleutian lows than in periods of weak Aleutian lows. Key to understanding the impact of climate change on Pacific salmon is understanding how the Aleutian low will change. Chinook and coho salmon are minor species in the total commercial catch, but important socially and economically in North America. A wise use of hatcheries may be needed to maintain abundances of these species in future decades.

Protandry in Pacific salmon

2000 ◽  
Vol 57 (6) ◽  
pp. 1252-1257 ◽  
Author(s):  
Yolanda Morbey
Keyword(s):  
Chinook Salmon ◽  
Sockeye Salmon ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Statistical Procedure ◽  
Timing Data ◽  
Mating Opportunities ◽  
Gender Specific ◽  
Specific Timing

Protandry, the earlier arrival of males to the spawning grounds than females, has been reported in several studies of Pacific salmon (Oncorhynchus spp.). However, the reasons for protandry in salmon are poorly understood and little is known about how protandry varies among and within populations. In this study, protandry was quantified in a total of 105 years using gender-specific timing data from seven populations (one for pink salmon (O. gorbuscha), three for coho salmon (O. kisutch), two for sockeye salmon (O. nerka), and one for chinook salmon (O. tshawytscha)). Using a novel statistical procedure, protandry was found to be significant in 90% of the years and in all populations. Protandry may be part of the males' strategy to maximize mating opportunities and may facilitate mate choice by females.

Effect of incubation temperature on the development of five species of Pacific salmon (Oncorhynchus) embryos and alevins

1988 ◽  
Vol 66 (1) ◽  
pp. 266-273 ◽  
Author(s):  
C. B. Murray ◽  
J. D. McPhail
Keyword(s):  
Chinook Salmon ◽  
Sockeye Salmon ◽  
Coho Salmon ◽  
Incubation Temperature ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Oncorhynchus Gorbuscha ◽  
Embryo Survival ◽  
Salmon Fry ◽  
Incubation Temperatures

Embryo and alevin survival, time to hatching and emergence, and alevin and fry size of five species of Pacific salmon (Oncorhynchus) were observed at five incubation temperatures (2, 5, 8, 11, and 14 °C). No pink (Oncorhynchus gorbuscha) or chum (O. keta) salmon embryos survived to hatching at 2 °C. Coho (O. kisutch) and sockeye (O. nerka) salmon had higher embryo survival at 2 °C than chinook (O. tschawytscha) salmon. At 14 °C, chum, pink, and chinook salmon had higher embryo survival than coho or sockeye salmon. In all species, peaks of embryo mortality occurred at specific developmental stages (completion of epiboly, eye pigmentation, and hatching). Alevin survival to emergence was high for all species, except for coho and pink salmon at 14 °C. Hatching and emergence time varied inversely with incubation temperature, but coho salmon hatched and emerged sooner at all temperatures than the other species. Coho and sockeye salmon alevins were larger at 2 °C, pink, chum, and chinook salmon alevins were larger at 5 and 8 °C. Coho salmon fry were larger at 2 °C, chinook and chum salmon fry were larger at 5 °C, and sockeye and pink salmon fry were larger at 8 °C. High incubation temperatures reduced fry size in all species. Each species of Pacific salmon appears to be adapted to different spawning times and temperatures, and thus indirectly to specific incubation temperatures, to ensure maximum survival and size and to maintain emergence at the most favorable time each year.

Review of the Rate of Growth and Mortality of Pacific Salmon in Salt Water, and Noncatch Mortality Caused by Fishing

1976 ◽  
Vol 33 (7) ◽  
pp. 1483-1524 ◽  
Author(s):  
W. E. Ricker
Keyword(s):  
Chinook Salmon ◽  
Sockeye Salmon ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
Salt Water ◽  
Pink Salmon ◽  
Total Yield ◽  
Coastal Region ◽  
Natural Mortality ◽  
Time Of Year

Mortality (other than landed catch) caused by pelagic gillnetting is estimated to be equal to the catch, for salmon in their penultimate year of life, and equal to about a quarter of the catch for salmon in their final year of life. Mortality caused by trolling for coho (Oncorhynchus kisutch) and chinook salmon (O. tshawytscha) averages about one fish killed (mostly below legal size) for every two that are boated. The natural mortality rate for sockeye salmon (O. nerka) in their final year of life averages about 0.015 per mo and is somewhat more in earlier years of pelagic life; the greater part of natural mortality after the smolt stage occurs during the downstream migration and early months of "coastal" life. For coho and chinook the best natural mortality estimate for the last year of life is 0.013 per mo, and that for pink (O. gorbuscha) and chum (O. keta) is of the same order. Growth rates during the final growing season vary from 0.26 per mo for pink and coho salmon to 0.06 per mo for chinook in their 5th ocean yr. Gains from ceasing to take immature salmon on the high seas range up to 300% of the catch now being taken in that category, while for fish taken in their final year they range up to about 70%, depending on the time of year at which the fishing is done. Gains from transferring existing pelagic net fisheries to the coastal region would be 76% (North American sockeye) and 86% (Asian sockeye) of the weight of fish now caught pelagically. Gains in total yield of existing salmon fisheries (pelagic and coastal) are estimated as 78% for Asian pink salmon and 72% for Asian sockeye. The increase in weight of the total catch from discontinuing ocean trolling for Columbia River chinook salmon and increasing river fishing correspondingly is estimated tentatively as between 63 and 98%.

scholarly journals Resources and fishery of Pacific salmon in Magadan region in the beginning of the 21st century

Trudy VNIRO ◽  
2020 ◽  
Vol 179 ◽  
pp. 90-102
Author(s):  
M. N. Gorokhov ◽  
V. V. Volobuev ◽  
I. S. Golovanov
Keyword(s):  
Chum Salmon ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Spawning Grounds ◽  
Magadan Region ◽  
Spawning Areas ◽  
Optimal Values ◽  
In The Beginning ◽  
Salmon Fishery

There are two main areas of pacific salmon fishing in the Magadan region: Shelikhova Gulf and Tauiskaya Bay. The main fishing species is pink salmon in the region. Its share of total salmon catch by odd-year returns reaches 85 %. Data on the dynamics of escapement to the spawning grounds of pink salmon of the Shelikhova Gulf and Tauiskaya Bay are presented. The displacement of the level of spawning returns of pink salmon into the Shelihova Gulf with the simultaneous reduction of its returns to the Tauiskaya Bay is shown. Data on the dynamics of the fishing indicators of pink salmon for the two main fishing areas are provided. The Tauiskaya Bay as the main pink salmon fishery area loses its importance is shown. Graphical data on the escapement of producers pink salmon to the spawning grounds are presented and the optimal values of spawning escapements are estimated. Chum salmon is the second largest and most fishing species. Information on the dynamics of the number of returns, catch and escapement to the spawning grounds of chum salmon is given. The indicators of escapement to the spawning areas and their compliance with the optimal passes of salmon producers are analyzed. The issues of the dynamics of returns number, catch and the escapement to the spawning grounds of coho salmon producers are considered. The level of the escapement to the spawning areas is shown and the ratio of actual to optimal values of passes is estimated. The role of coho salmon as an object of industrial fishing and amateur fishing is shown. The extent of fishing press on individual groups of salmon populations is discussed. It is concluded that it is necessary to remove the main salmon fishery from the Tauiskaya Bay to the Shelikhova Gulf.

scholarly journals Pacific salmon abundance trends and climate change

2011 ◽  
Vol 68 (6) ◽  
pp. 1122-1130 ◽  
Author(s):  
James R. Irvine ◽  
Masa-aki Fukuwaka
Keyword(s):  
Climate Change ◽  
Pacific Ocean ◽  
North Pacific ◽  
Sockeye Salmon ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
North Pacific Ocean ◽  
Pink Salmon ◽  
The North ◽  
Abundance Trends

Abstract Irvine, J. R., and Fukuwaka, M. 2011. Pacific salmon abundance trends and climate change. – ICES Journal of Marine Science, 68: 1122–1130. Understanding reasons for historical patterns in salmon abundance could help anticipate future climate-related changes. Recent salmon abundance in the northern North Pacific Ocean, as indexed by commercial catches, has been among the highest on record, with no indication of decline; the 2009 catch was the highest to date. Although the North Pacific Ocean continues to produce large quantities of Pacific salmon, temporal abundance patterns vary among species and areas. Currently, pink and chum salmon are very abundant overall and Chinook and coho salmon are less abundant than they were previously, whereas sockeye salmon abundance varies among areas. Analyses confirm climate-related shifts in abundance, associated with reported ecosystem regime shifts in approximately 1947, 1977, and 1989. We found little evidence to support a major shift after 1989. From 1990, generally favourable climate-related marine conditions in the western North Pacific Ocean, as well as expanding hatchery operations and improving hatchery technologies, are increasing abundances of chum and pink salmon. In the eastern North Pacific Ocean, climate-related changes are apparently playing a role in increasing chum and pink salmon abundances and declining numbers of coho and Chinook salmon.

Sexual Dimorphism in the Adipose Fin of Pacific Salmon (Oncorhynchus)

1983 ◽  
Vol 40 (11) ◽  
pp. 2019-2024 ◽  
Author(s):  
Terry D. Beacham ◽  
Clyde B. Murray
Keyword(s):  
Sexual Dimorphism ◽  
Chinook Salmon ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Relative Size ◽  
Correct Identification ◽  
Actual Amount ◽  
Adipose Fin

Male adipose fins of Oncorhynchus species were 30–50% larger than those of same-sized females, the actual amount depending on the species. Accuracy of classification of the standards ranged from 87% in chinook salmon (O. tshawytscha) to 98% in pink salmon (O. gorbuscha). Testing the method on new samples usually resulted in an accuracy of at least 90% correct identification of sex for any species. Relative size of the adipose fin should allow for easy and accurate external identification of the sexes of silver-bright Oncorhynchus.

Changes in the Average Size and Average Age of Pacific Salmon

1981 ◽  
Vol 38 (12) ◽  
pp. 1636-1656 ◽  
Author(s):  
W. E. Ricker
Keyword(s):  
Growth Rate ◽  
Chinook Salmon ◽  
Sockeye Salmon ◽  
Oncorhynchus Tshawytscha ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
Gill Nets ◽  
Growing Seasons ◽  
Mean Size ◽  
Average Size

Of the five species of Pacific salmon in British Columbia, chinook salmon (Oncorhynchus tshawytscha) and coho salmon (O. kisutch) are harvested during their growing seasons, while pink salmon (O. gorbuscha), chum salmon (O. keta), and sockeye salmon (O. nerka) are taken only after practically all of their growth is completed. The size of the fish caught, of all species, has decreased, but to different degrees and over different time periods, and for the most part this results from a size decrease in the population. These decreases do not exhibit significant correlations with available ocean temperature or salinity series, except that for sockeye lower temperature is associated with larger size. Chinook salmon have decreased greatly in both size and age since the 1920s, most importantly because nonmaturing individuals are taken by the troll fishery; hence individuals that mature at older ages are harvested more intensively, which decreases the percentage of older ones available both directly and cumulatively because the spawners include an excess of younger fish. Other species have decreased in size principally since 1950, when the change to payment by the pound rather than by the piece made it profitable for the gill-netters to harvest more of the larger fish. Cohos and pinks exhibit the greatest decreases, these being almost entirely a cumulative genetic effect caused by commercial trolls and gill nets removing fish of larger than average size. However, cohos reared in the Strait of Georgia have not decreased in size, possibly because sport trolling has different selection characteristics or because of the increase in the hatchery-reared component of the catch. The mean size of chum and sockeye salmon caught has changed much less than that of the other species. Chums have the additional peculiarity that gill nets tend to take smaller individuals than seines do and that their mean age has increased, at least between 1957 and 1972. That overall mean size has nevertheless decreased somewhat may be related to the fact that younger-maturing individuals grow much faster than older-maturing ones; hence excess removal of the smaller younger fish tends to depress growth rate. Among sockeye the decrease in size has apparently been retarded by an increase in growth rate related to the gradual cooling of the ocean since 1940. However, selection has had two important effects: an increase in the percentage of age-3 "jacks" in some stocks, these being little harvested, and an increase in the difference in size between sockeye having three and four ocean growing seasons, respectively.Key words: Pacific salmon, age changes, size changes, fishery, environment, selection, heritability

scholarly journals The orientation and migratory dynamics of the western rock lobster, Panulirus cygnus, in Western Australia

2014 ◽  
Vol 71 (5) ◽  
pp. 1052-1063 ◽  
Author(s):  
Simon de Lestang
Keyword(s):  
Large Scale ◽  
Economic Benefits ◽  
Rock Lobster ◽  
Commercial Catch ◽  
Breeding Grounds ◽  
Mean Size ◽  
Catch Rates ◽  
Panulirus Cygnus ◽  
The Impact ◽  
Oceanic Currents

Abstract Large-scale migrations are known to occur in numerous species, and in the case of the Western Rock Lobster, Panulirus cygnus, result in juveniles moving from nursery areas into deeper offshore breeding grounds. In 2008 the Western Rock Lobster fishery reduced harvest rates to increase legal and spawning biomass throughout the fishery, which also allowed greater numbers of lobsters to migrate. Increased lobster migration could potentially reduce biomass in some areas, thus adversely impacting commercial catch rates. Over 20 000 tag–recaptured lobsters were analysed to determine the dynamics underlying migration in this species and to assess the impact reduced harvest rates may have had on catches. This study showed that P. cygnus migration was associated with body size and water depth, and that magnetism and oceanic currents appear to be the most likely guideposts used for orientation. Size at migration varied in a constant fashion along the coast, being larger towards the southern end of the fishery and smallest at the offshore Abrolhos Islands. During the migration period, up to 50% of lobsters at their mean size of migration moved from coastal areas out towards deeper waters (>40 m), whereas <15% of those in deeper water at the same size moved significant distances northward. This behaviour appears to be contranatant, counteracting the downstream redistribution of larvae after their 9–11 month larval life. Reduced harvest rates and catches being focussed onto higher valued sedentary lobsters have allowed more lobsters to migrate. However, the numbers moving between management areas are relatively small, with the biological and economic benefits of fishing at a reduced exploitation rate outweighing losses to catches.

Production of germline transgenic Pacific salmonids with dramatically increased growth performance

1995 ◽  
Vol 52 (7) ◽  
pp. 1376-1384 ◽  
Author(s):  
Robert H. Devlin ◽  
Timothy Y. Yesaki ◽  
Edward M. Donaldson ◽  
Shao Jun Du ◽  
Choy-Leong Hew
Keyword(s):  
Chinook Salmon ◽  
Oncorhynchus Tshawytscha ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
Cutthroat Trout ◽  
Transgenic Fish ◽  
Somatic Tissue ◽  
Growth Enhancement ◽  
Gene Construct ◽  
Average Size

Transgenic Pacific salmon have been produced by microinjection of a DNA construct consisting of chinook salmon (Oncorhynchus tshawytscha) growth hormone sequences driven by an ocean pout (Macrozoarces americanus) antifreeze protein promoter. This construct was retained in approximately 4% of fish derived from injected eggs, and resulted in dramatic enhancement of growth relative to controls. For coho salmon (O. kisutch) at 15 months of age, the average size of transgenic fish was more than 10-fold that of controls, with the largest fish more than 30-fold larger than nontransgenic siblings. Dramatic growth enhancement was also observed in transgenic rainbow trout (O. mykiss), cutthroat trout (O. clarki), and chinook salmon using this same gene construct. Transgenic coho salmon underwent precocious parr–smolt transformation during their first fall, approximately 6 months in advance of their nontransgenic siblings. At 2 years of age, five male transgenic coho salmon became sexually mature, and four of these transmitted the gene construct to sperm, the negative fish being transgenic in blood but not fin tissue. These results show that while some fish are mosaic for the gene construct in different tissues, most are transgenic in both germline and somatic tissue.

scholarly journals Climate and competition influence sockeye salmon population dynamics across the Northeast Pacific Ocean

2020 ◽  
Vol 77 (6) ◽  
pp. 943-949 ◽  
Author(s):  
Brendan Connors ◽  
Michael J. Malick ◽  
Gregory T. Ruggerone ◽  
Pete Rand ◽  
Milo Adkison ◽  
...  
Keyword(s):  
Sockeye Salmon ◽  
Large Scale ◽  
Pacific Salmon ◽  
Spatial Scales ◽  
Interspecific Interactions ◽  
Pink Salmon ◽  
Oncorhynchus Gorbuscha ◽  
Negative Effects ◽  
Positive Effects ◽  
The North

Pacific salmon productivity is influenced by ocean conditions and interspecific interactions, yet their combined effects are poorly understood. Using data from 47 North American sockeye salmon (Oncorhynchus nerka) populations, we present evidence that the magnitude and direction of climate and competition effects vary over large spatial scales. In the south, a warm ocean and abundant salmon competitors combined to strongly reduce sockeye productivity, whereas in the north, a warm ocean substantially increased productivity and offset the negative effects of competition at sea. From 2005 to 2015, the approximately 82 million adult pink salmon (Oncorhynchus gorbuscha) produced annually from hatcheries were estimated to have reduced the productivity of southern sockeye salmon by ∼15%, on average. In contrast, for sockeye at the northwestern end of their range, the same level of hatchery production was predicted to have reduced the positive effects of a warming ocean by ∼50% (from a ∼10% to a ∼5% increase in productivity, on average). These findings reveal spatially dependent effects of climate and competition on sockeye productivity and highlight the need for international discussions about large-scale hatchery production.

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