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Domestication and selective breeding for rapid-growth have impaired the cardiorespiratory system of salmonids, which might compromise their capacity to tolerate environmental stressors, such as heat waves. Exercise training by swimming has been proposed as a potential tool to enhance growth, cardiac function and disease resilience in farmed fish and thereby improves aquaculture production. However, whether exercise training could also improve cardiac robustness against heat waves, which are becoming more common and cause severe challenges to aquaculture, remains unknown. Here, we trained juvenile rainbow trout at three different training velocities: 0.06 m*s-1 (or 0.9 body lengths per second [bl*s-1]; control group), 0.11 m*s-1 (or 1.7 bl*s-1; medium speed group) and 0.17 m*s-1 (or 2.7 bl*s-1; high speed group) for 5 weeks, 6h per day, 5 days per week. Measuring maximal heart rate (fHmax) during acute warming, we demonstrated that training at 1.7 bl*s-1 was optimal in order to increase the temperature at which fHmax reached its peak (Tpeak) as well as the upper thermal tolerance of the cardiovascular function (arrhythmia temperature, TARR), up to 3.6°C as compared to the control fish. However, more intensive training did not provide similar improvement on thermal tolerance. Both training regimes enhanced the ventricular citrate synthase activity which may provide higher aerobic energy production capacity for ventricles. Further mechanistic studies are needed to understand the complex interactions between training intensities and changes in thermal tolerance. Although not conclusive on that point, our findings present a valid training programme for hatchery salmonids to increase their cardiac thermal tolerance and consequently probably also their capacity to tolerate heat waves, which has a direct application for aquaculture.

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Phenotypic plasticity manifested after acclimatization is a very important source of biological variability among fish species. We hypothesized that hypoxic acclimation, besides potentially generating a temporary hypoxic respiratory phenotype, would also manifest as a continued benefit after re-acclimation to normoxia. Hence, we holistically characterized the respiratory phenotype of European sea bass (Dicentrarchus labrax) acclimated to normoxia with or without prior acclimation to hypoxia. Compared with the original normoxic phenotype, prior acclimation to hypoxia and return to normoxia produced a 27% higher absolute aerobic scope (AAS), a 24% higher citrate synthase activity in red muscle and a 28% lower excess post-exercise O2 consumption. Additional testing of hypoxia-acclimated fish under normoxia explored the specific effects of hypoxic acclimation. The hypoxic phenotype, when compared with the original normoxic phenotype, had a lower standard metabolic rate, a better hypoxia performance and a lower minimum PO2 for supporting 50% AAS. Given this respiratory malleability, general predictions for marine fish exploiting a more hypoxic future should better consider respiratory plasticity and prolonged effects of hypoxic exposures.

Carryover effects of environmental stressors occur when experiences of the environment in earlier life stages or seasons influence the performance of individuals later in life. These can be especially critical for species that have diverse developmental transition periods in their life cycle, such as salmonid fish. Sublethal changes in metabolism, size, or growth experienced in early life stages may have a long‐lasting effect on the subsequent life performance of these species, but very few studies have formally tested these changes in relation to environmental stressors. Here, we investigated whether different types of fine sediment result in carryover effects that change the life performance of migratory brown trout. First, we manipulated the early habitat conditions of brown trout through the life stages from egg to fry by incubating them in varying substrate treatments (i.e., gravel without added sediment, gravel with added fine sand, and gravel with added organic matter). Exposure to fine sediment during early development had serious effects on the metabolism, size, escape responses, timing of emergence, and potential survival of early life stages. These carryover effects were persistent and remained present over the critical life shift from relying on parentally provided resources as immobile eggs to independent exogenous feeding as parr. Second, fish were relocated as parr to either their original or different treatment environments and their metabolism, size, and growth were reanalyzed. The effects of environmental stress were observed later in their life cycle when fry from the gravel treatment were relocated to sand or organic‐rich treatments. These were found to be significantly smaller in size and had a higher metabolic rate than fry maintained in their original treatment environment. Together, our study experimentally demonstrated that the carryover effects of environmental stressors experienced in early stages may influence the fitness outcomes of migratory fish later in life. We suggest that sublethal environmental stressors should be better considered in restoration schemes and management strategies to reverse the current trend of declining salmonid populations.