Abstract
ABSTRACTHoming with high fidelity to natal spawning grounds for reproduction is a hallmark of anadromous Pacific salmon biology, although low rates of dispersal (‘straying’) also occurs. Currently little is known about the proximate factors influencing straying, which limits our understanding of this fundamental biological phenomenon and impedes options for reducing straying-mediated interactions between wild and hatchery-produced individuals. We explored the potential role of stress experienced in captivity prior to intentional release to manifest in developmental irregularities and potentially influence rates of straying by adults. We compared two proxies for stress between groups of hatchery-produced individuals that had homed back to the hatchery or strayed to non-natal streams compared to wild individuals that were presumed to have homed to a wild spawning stream. Blood plasma cortisol was used to assess stress at the terminus of their migration, and percent frequency of vateritic otolith development within groups as a measure of stresses incurred during development. We found no evidence that either proxy for stress was associated with straying. No differences in cortisol concentrations were found between wild and hatchery-produced chum salmon that had homed or strayed, either in males (wild=95.9±175.7 ng/ml; stray=113.4±99.7 ng/ml; home=124.7±113.8 ng/ml) or females (wild=307.6±83.4 ng/ml; stray= 329.0±208.9 ng/ml; home=294.1±134.8 ng/ml); however, significant differences between males and females occurred in each group. The percent frequency of vaterite occurrence in otoliths of hatchery-produced chum salmon that either strayed (40% vaterite) or homed (45% vaterite) did not differ significantly, though rates of vaterite occurred less frequently in wild chum salmon (24%), which is consistent with other studies. Mass thermal marking of juvenile fish in hatcheries is unlikely to increase vateritic development as neither intensity (number of temperature changes) or complexity (number of temperature change sequences) of the mark was associated with frequency of vaterite occurrence. Though not associated with straying, cortisol concentrations were associated with shorter instream lifespan of both hatchery and wild individuals but did not appear to influence rates of egg retention in spawning females, suggesting an equivocal role in reproductive ecology. Our results are suggestive that stress induced during the early stages of rearing in a hatchery environment from marking or other causes may not increase straying later in life, though the higher rates of vaterite observed in hatchery-produced fish may come at a cost of increased marine mortality, due to the otoliths' role in navigation and hearing.
Highlights
Homing of Pacific salmon (Oncorhynchus spp.) to natal sites for reproduction is entwined with the ecology, evolution and management of the species (Myers et al, 1998; Dittman and Quinn, 1996)
Frequency of vaterite occurrence, straying and thermal mark intensity Thermal marking was not associated with percent frequency of vaterite occurrence regardless of thermal marking intensity (z=1.27, P=0.203), complexity (z=1.27, P=0.259), or duration (z=1.36, P=0.172) between different hatchery groups of chum salmon from Southeast Regional Aquaculture Association (SSRAA)
Rates of vaterite occurrence did not differ between hatchery-produced strays (Hps) (40% vaterite) and hatchery-produced home (Hph) (45% vaterite) chum salmon (Z-test; Z score=1.22, P=0.222) despite our ability to control for brood-year effects and using groups with large sample sizes (Table 1)
Summary
Homing of Pacific salmon (Oncorhynchus spp.) to natal sites for reproduction is entwined with the ecology, evolution and management of the species (Myers et al, 1998; Dittman and Quinn, 1996). Physiology and behavior of a wide range of taxa are mediated by hormone production and monitoring those hormone levels are often useful in understanding life history variations within species (Crespi et al, 2013). Stress-inducing situations stimulate the HPA to increase production of glucocorticoid’s to meet energetic demands of perceived challenges to homeostasis (Wingfield and Sapolsky, 2003). This temporary increase in hormone production above basal levels is commonly measured as an acute stress response and used in models as an explanatory variable to predict various life history and behavioral responses (Crespi et al, 2013)
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