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Atlantic cod (Gadus morhua) caught in recreational fisheries are commonly released, often with barotrauma after rapid decompression. Mouth-hooked, non-bleeding cod kept in a floating net pen showed mortalities ≥40% when angled from >50 m depth, likely because of cumulative stress from ongoing barotrauma and exposure to warm surface water. In a natural setting, however, cod have the opportunity to descend after release and are not restricted to the surface. In a follow-up study, 97.8% of similarly selected cod managed to dive following immediate release, whereas 2.2% were floaters. No mortality was observed for divers kept in cages, which were lowered to capture depth for 72 h. While the floaters would likely have died in a natural setting, no mortality was observed when they were recompressed and kept at capture depth for 72 h. The occurrence of swim bladder ruptures, swollen coelomic cavities, venous gas embolisms, and gas release around the anus was significantly influenced by capture depth (range 0–90 m). A supplementary radiology study showed inflated swim bladders in 87% of the cod after 72 h, and most barotrauma signs had disappeared after 1 month. This study encourages investigation of survival potential for physoclistous species when high mortalities are assumed but undocumented. Matching natural post-release and containment environment is essential in the experimental setup, as failure to do so may bias survival estimates, particularly when a thermocline is present. Assuming minimal predation, short-term mortality of cod experiencing barotrauma is negligible if cod submerge quickly by themselves and are otherwise not substantially injured. Survival of floaters may be increased by forced recompression to capture depth. Sublethal and long-term impacts of barotrauma remain to be studied. To ensure that cod have sufficient energy to submerge, anglers are encouraged to avoid fighting the fish to exhaustion and to minimize handling before release.

The aim of the present study was to investigate cataract development in diploid (2N) and triploid (3N) Atlantic salmon smolts and post-smolts at two water temperatures (10 and 16°C) given diets with different histidine supplementation (LH, 10.4 and HH, 13.1 g kg À1 ) before and after seawater transfer. In freshwater, a severe cataract outbreak was recorded in both ploidies reared at 16°C. The cataract score was significantly higher in triploids compared to diploids, and the severity was lower in both ploidies fed the HH diet. The cataract development at 10°C was minor. Low gill Na + , K + -ATPase activity in fish reared at 16°C before seawater transfer was followed by osmoregulatory stress with elevated plasma electrolyte concentrations and high mortality in sea water. Both diploids and triploids reared at 10°C developed cataracts during the seawater period, with higher severities in triploids than diploids and a reduced severity in the fish fed the HH diet. The findings of this study demonstrate the importance of environmental conditions in the husbandry of Atlantic salmon, and particularly triploids, with regard to smoltification and adjusted diets to mitigate cataract development in fresh and sea water.

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In salmon farming, the use of sterile triploids (3N) can mitigate the problem of escapees interbreeding with wild salmon. However, triploid salmon appear less tolerant to high water temperatures and low oxygen levels compared to diploids (2N). To investigate how the thermal performance and physiology of large (2.5 kg) triploid Atlantic salmon Salmo salar L. differs from those of diploids, both ploidies were subjected to water temperatures between 3 and 18°C. The fish were exposed to reduced oxygen saturations (O 2 sat , 70%), termed hypoxia, at 6 and 18°C. Triploids fed more than diploids between 3 and 9°C and at similar levels at 12°C. At 15°C, the feed intake significantly dropped in both ploidies, although more in triploids. During hypoxia, feed intake was higher in triploids at 6°C and equal to diploids at 18°C. The overall feed conversion ratio was similar between ploidies. Muscle energy phosphates were generally lower in triploids than diploids, while muscle glucose, blood haemoglobin and haematocrit were lower in triploids than diploids at ≥12°C. Plasma lactate levels tended to be higher in triploids and increased with increasing temperature and at hypoxia in both ploidies. Plasma cortisol increased in both ploidies at high temperatures and was highest in triploids under hypoxic conditions at 18°C. Triploids had a higher cataract score at the start of the experiment and developed more cataracts throughout the experiment. The present findings show that large triploid Atlantic salmon perform better at colder water temperatures compared to diploids and differ in parts of their physiological expression at increasing and high temperature.