The effects of ocean conditions on highly migratory species such as salmon are difficult to assess owing to the diversity of environments they encounter during their marine life. In this study, we reconstructed the initial ocean migration routes of juvenile Chinook salmon Oncorhynchus tshawytscha originating from Oregon to Southeast Alaska using coded wire tag recovery data from Canadian Department of Fisheries and Oceans and National Marine Fisheries Service research surveys conducted between 1995 and 2006. Over this 12-year period, 1,862 coded-wire-tagged juvenile Chinook salmon were recovered along the coasts of Oregon, Washington, British Columbia, and Alaska from March to November. Except for those from the Columbia River, most juvenile Chinook salmon remained within 100-200 km of their natal rivers until their second year at sea, irrespective of their freshwater history and adult run timing. Northward migration of most coastal stocks was initiated during their second or possibly third year at sea, whereas the Strait of Georgia and Puget Sound stocks primarily migrated onto the continental shelf after their first year at sea. In contrast, Columbia River Chinook salmon generally undertook a rapid northward migration that varied among life histories and stocks. Columbia River spring Chinook salmon were recovered as far north as Prince William Sound, Alaska, during their first summer at sea, whereas very few Columbia River fall Chinook salmon were recovered north of Vancouver Island. In addition to northern migrants, a fraction of the Columbia River spring and fall Chinook salmon actively migrated south of the Columbia River. The stock-specific initial ocean migration routes described in this study will aid in the identification of the appropriate spatial and temporal scales for assessing the processes regulating Chinook salmon recruitment in the marine environment.
Marine growth and survival of juvenile Chinook salmon Oncorhynchus tshawytscha depend in part on the quality and quantity of prey consumed during this potentially critical life stage; however, little is known about the early marine diet of these fish or factors that affect the diet's variability. We examined the recent
page 361 Introduction 361 Material and methods 364 Results 364 Discussion 366 References 368Abstract Otoliths, or 'ear stones', are calcium carbonate structures found in all vertebrates. In teleosts, they have a number of sensory functions, including hearing. Daily growth increments of these structures have permitted advanced age and population studies of teleosts. Whereas 'normal' otoliths are composed of crystals imbedded within a protein matrix as aragonite, a 'crystalline' form of calcium carbonate termed vaterite is also found. A review of the otolith literature demonstrates a significant level of understanding of the structure and function of otoliths, but the cause for crystalline otolith structure remains speculative. Pairs of otoliths from hatchery and wild juvenile and adult coho salmon (Oncorhynchus kisutch) were examined visually for determination of otolith microstructure type. The vateritic or crystalline otoliths were found in much higher percentages in juvenile hatchery-reared coho salmon than in juvenile wild coho salmon, supporting previous studies. There did not seem to be any negative impact on size or survival. There was also no correlation between crystalline otoliths and premature maturation in coho males. A preliminary study of adult coho salmon returning to Big Qualicum and Chilliwack hatcheries showed even higher ratios of vateritic otoliths than observed in juveniles.
An analysis of the results of a 10‐year study of the population ecology of juvenile hatchery and wild coho salmon Oncorhynchus kisutch in the Strait of Georgia produced new information about the interannual and interseasonal fluctuations in abundance and marine survival. A decline in the percentage of hatchery coho salmon was related to declines in hatchery fish abundance and marine survival; wild coho salmon abundance was more stable. The declining marine survival of hatchery coho salmon appeared to be related to a fixed average date of release from hatcheries and a possibility of earlier prey production. The relatively stable abundance of wild coho salmon may relate to a natural trend toward earlier ocean entry dates. Oscillations in hatchery coho salmon percentage and abundance were related to oscillations in abundance of juvenile pink salmon O. gorbuscha. The impact of oscillating density affected marine survival of hatchery coho salmon more than that of wild coho salmon. Marine survival and abundance of hatchery and wild coho salmon in July were positively related to average fork length, indicating that growth within the first few months after ocean entry affected marine survival. However, absolute size was not important, as wild coho salmon were consistently smaller than hatchery coho salmon. Wild coho salmon responded to conditions in the marine ecosystem differently than hatchery coho salmon, as relationships among growth, survival, and abundance were apparent for wild coho salmon earlier in the year than for hatchery fish. The length increase between July and September was inversely related to marine survival, suggesting that fish that were larger in July grew less and survived better because they were storing more lipids than smaller coho salmon. The study indicated that a more experimental management strategy is needed for both hatchery and wild coho salmon.
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