Background Data storage tags (DSTs) record and store information about animals and their environment, and can provide important data relevant to fish culture, ecology and conservation. A DST has recently been developed that records heart rate (fH), electrocardiograms (ECGs), tri-axial acceleration and temperature. However, at the time of this study, no research using these tags had been performed on fish or determined the quality of the data collected. Thus, our research asked: do these DSTs provide reliable and meaningful data? To examine this question, Atlantic salmon (1.4 ± 0.7 kg) were implanted with DSTs, then swam at increasing speeds in a swim tunnel after 1 week of recovery. Further, in two separate experiments, salmon (2.4 ± 0.1 kg) were implanted with DSTs and held in a large tank with conspecifics for 1 week at 11 °C or 6 weeks at 8–12 °C. Results External acceleration (EA) and variation in EA (VAR) increased exponentially with swimming speed and tail beat frequency. The quality index (QI) assigned to ECG recordings (where QI0 means very good quality, and QI1, QI2 and QI3 are of reduced quality) did not change significantly with increasing swimming speed (QI0 ~ 60–80%). However, we found that the accuracy of the tag algorithm in estimating fH from ECGs was reduced when QI>0. Diurnal patterns of fH and EA were evident from the time the salmon were placed in the tank. Heart rate appeared to stabilize by ~ 4 days post-surgery in the first experiment, but extended holding showed that fH declined for 2–3 weeks. During extended holding, the tag had difficulty recording low fH values < 30 bpm, and for this reason, in addition to the fact that the algorithm can miscalculate fH, it is highly recommended that ECGs be saved when possible for quality control and so that fH values with QI>0 can be manually calculated. Conclusions With these DSTs, parameters of acceleration can be used to monitor the activity of free-swimming salmon. Further, changes in fH and heart rate variability (HRV) due to diurnal rhythms, and in response to temperature, activity and stressors, can be recorded.

Background: Climate change is leading to increased water temperatures and reduced oxygen levels at sea-cage sites, and this is a challenge that the Atlantic salmon aquaculture industry must adapt to it if it needs to grow sustainably. However, to do this, the industry must better understand how sea-cage conditions influence the physiology and behavior of the fish.Method: We fitted ~2.5 kg Atlantic salmon on the south coast of Newfoundland with Star-Oddi milli-HRT ACT and Milli-TD data loggers (data storage tags, DSTs) in the summer of 2019 that allowed us to simultaneously record the fish's 3D acceleration (i.e., activity/behavior), electrocardiograms (and thus, heart rate and heart rate variability), depth, and temperature from early July to mid-October.Results: Over the course of the summer/fall, surface water temperatures went from ~10–12 to 18–19.5°C, and then fell to 8°C. The data provide valuable information on how cage-site conditions affected the salmon and their determining factors. For example, although the fish typically selected a temperature of 14–18°C when available (i.e., this is their preferred temperature in culture), and thus were found deeper in the cage as surface water temperatures peaked, they continued to use the full range of depths available during the warmest part of the summer. The depth occupied by the fish and heart rate were greater during the day, but the latter effect was not temperature-related. Finally, while the fish generally swam at 0.4–1.0 body lengths per second (25–60 cm s−1), their activity and the proportion of time spent using non-steady swimming (i.e., burst-and-coast swimming) increased when feeding was stopped at high temperatures.Conclusion: Data storage tags that record multiple parameters are an effective tool to understand how cage-site conditions and management influence salmon (fish) behavior, physiology, and welfare in culture, and can even be used to provide fine-scale mapping of environmental conditions. The data collected here, and that in recent publications, strongly suggest that pathogen (biotic) challenges in combination with high temperatures, not high temperatures + moderate hypoxia (~70% air saturation) by themselves, are the biggest climate-related challenge facing the salmon aquaculture industry outside of Tasmania.

Fish nursery habitats are increasingly hypoxic and the brain is recognized as highly hypoxia-sensitive, yet there is a lack of information on the effects of hypoxia on the development and function of the larval fish brain. Here, we tested the hypothesis that by inhibiting brain development, larval exposure to severe hypoxia has persistent functional effects on the cortisol stress response in zebrafish (Danio rerio). Exposing 5 days post-fertilization (dpf) larvae to 10% dissolved O2 (DO) for 16 h only marginally reduced survival, but it decreased forebrain neural proliferation by 55%, and reduced the expression of neurod1, gfap, and mbpa, markers of determined neurons, glia, and oligodendrocytes, respectively. The 5 dpf hypoxic exposure also elicited transient increases in whole body cortisol and in crf, uts1, and hsd20b2 expression, key regulators of the endocrine stress response. Hypoxia exposure at 5 dpf also inhibited the cortisol stress response to hypoxia in 10 dpf larvae and increased hypoxia tolerance. However, 10% DO exposure at 5 dpf for 16h did not affect the cortisol stress response to a novel stressor in 10 dpf larvae or the cortisol stress response to hypoxia in adult fish. Therefore, while larval exposure to severe hypoxia can inhibit brain development, it also increases hypoxia tolerance. These effects may transiently reduce the impact of hypoxia on the cortisol stress response but not its functional capacity to respond to novel stressors. We conclude that the larval cortisol stress response in zebrafish has a high capacity to cope with severe hypoxia-induced neurogenic impairment.

Studies on the effects of environmental changes with increasing depth (e.g. temperature and oxygen level) on fish physiology rarely consider how hydrostatic pressure might influence the observed responses. In this study, lumpfish (Cyclopterus lumpus, 200–400 g), which can exhibit vertical migrations of over 100 m daily and can be found at depths of 500 m or more, were implanted with Star-Oddi micro-HRT loggers. Then, their heart rate (fH) was measured in a pressure chamber when exposed to the following: (i) increasing pressure (up to 80 bar; 800 m in depth) at 10°C or (ii) increasing temperature (12–20°C), decreasing temperature (12 to 4°C) or decreasing oxygen levels (101–55% air saturation at 12°C) in the absence or presence of 80 bar of pressure. Additionally, we determined their fH response to chasing and to increasing temperature (to 22°C) at atmospheric pressure. Pressure-induced increases in fH (e.g. from 48 to 61 bpm at 12°C) were associated with hyperactivity. The magnitude of the rise in fH with temperature was greater in pressure-exposed vs. control fish (i.e. by ~30 bpm vs. 45 bpm between 5°C and 20°C). However, the relative increase (i.e. slope of the relationship) was not different between groups. In contrast, 80 bar of pressure eliminated the small (5 bpm) increase in fH when control fish were exposed to hypoxia. Exhaustive exercise and increasing temperature to 22°C resulted in a maximum fH of 77 and 81 bpm, respectively. Our research shows that pressure influences the fH response to environmental challenges and provides the first evidence that lumpfish have a limited capacity to increase fH.

The increasing popularity of catch-andrelease angling indicates a need to identify best practices that minimize sublethal injuries, impairments, and mortality. One factor impacting the viability of catch and release is the risk of hooking injury, which can impact survival in released fishes. In particular, deep hooking is known to increase post-release mortality in numerous species. As such, best practices include the use of equipment and promotion of angler behaviors that reduce incidences of deep hooking. In some areas, angling at night is restricted because of concerns that deep hooking is elevated relative to angling during the day. However, there has been little empirical research investigating whether deep hooking is influenced by the time of day (light levels). In the present study, we captured bluegill (Lepomis macrochirus Rafinesque, 1810) and pumpkinseed (Lepomis gibbosus Linnaeus, 1758) using active angling (cast and retrieve) and passive angling (with a bobber) throughout the 24-hr period, and recorded hook depth and hook location for each fish. We found that passive angling methods resulted in deeper hooking than active angling methods for both bluegill and pumpkinseed across all time periods. Although few pumpkinseed were caught at night, we found that the pumpkinseed caught were hooked more deeply and in more damaging hooking locations at night relative to the day. Hooking injury was independent of diel period for the more frequently landed species, bluegill. These findings emphasize the species-specific nature of catch-and-release outcomes, and suggest that further research is warranted to adequately quantify the impacts of recreational fishing at night.