Behaviour represents a reaction to the environment as fish perceive it and is therefore a key element of fish welfare. This review summarises the main findings on how behavioural changes have been used to assess welfare in farmed fish, using both functional and feeling-based approaches. Changes in foraging behaviour, ventilatory activity, aggression, individual and group swimming behaviour, stereotypic and abnormal behaviour have been linked with acute and chronic stressors in aquaculture and can therefore be regarded as likely indicators of poor welfare. On the contrary, measurements of exploratory behaviour, feed anticipatory activity and reward-related operant behaviour are beginning to be considered as indicators of positive emotions and welfare in fish. Despite the lack of scientific agreement about the existence of sentience in fish, the possibility that they are capable of both positive and negative emotions may contribute to the development of new strategies (e.g. environmental enrichment) to promote good welfare. Numerous studies that use behavioural indicators of welfare show that behavioural changes can be interpreted as either good or poor welfare depending on the fish species. It is therefore essential to understand the species-specific biology before drawing any conclusions in relation to welfare. In addition, different individuals within the same species may exhibit divergent coping strategies towards stressors, and what is tolerated by some individuals may be detrimental to others. Therefore, the assessment of welfare in a few individuals may not represent the average welfare of a group and vice versa. This underlines the need to develop on-farm, operational behavioural welfare indicators that can be easily used to assess not only the individual welfare but also the welfare of the whole group (e.g. spatial distribution). With the ongoing development of video technology and image processing, the on-farm surveillance of behaviour may in the near future represent a low-cost, noninvasive tool to assess the welfare of farmed fish.
Behaviour represents a reaction to the environment as fish perceive it and is therefore a key element of fish welfare. This review summarises the main findings on how behavioural changes have been used to assess welfare in farmed fish, using both functional and feeling-based approaches. Changes in foraging behaviour, ventilatory activity, aggression, individual and group swimming behaviour, stereotypic and abnormal behaviour have been linked with acute and chronic stressors in aquaculture and can therefore be regarded as likely indicators of poor welfare. On the contrary, measurements of exploratory behaviour, feed anticipatory activity and rewardrelated operant behaviour are beginning to be considered as indicators of positive emotions and welfare in
In two experiments, a computerized on-demand feeding system coupled with a PIT tag monitoring device was used to continuously record the triggering activity by ca. 50 individual sea bass for 55 days (Exp. 1, initial average body weight and coefficient of variation, CV: 299 g, 15%) and 69 days (Exp. 2, 157 g, 13%). Each group was stocked in 1 m3 tanks and exposed to a water temperature of 21 ± 1 °C and a light regime of 16:8 LD. Only 5% of the triggering activity was not associated with simultaneous PIT tag detection. Although each individual was detected via PIT tag during the experiment, only 67% and 74% of the fish actuated the trigger at least once in Exp. 1 and Exp. 2, respectively. Moreover, only two fish in Exp. 1 and one fish in Exp. 2 accounted for 82% (43 + 39) and 77% of the total triggering activity, respectively. These three, high-triggering individuals did not exhibit a higher specific growth rate or agonistic behavior as observed by video monitoring. Indeed, zero-triggering fish had either a slightly higher SGR (Exp. 1) or a higher final body weight (Exp. 2) compared with low-and high-triggering fish.
In Teleost fish, development, growth, and reproduction are influenced by the daily and seasonal variations of photoperiod and temperature. Early in vivo studies indicated the pineal gland mediates the effects of these external factors, most probably through the rhythmic production of melatonin. The present investigation was aimed at determining whether melatonin acts directly on the pituitary to control GH and prolactin (PRL) secretion in rainbow trout. We show that 2-[125I]-iodomelatonin, a melatonin analog, binds selectively to membrane preparations and tissue sections from trout pituitaries. The affinity was within the range of that found for the binding to brain microsomal preparations, but the number of binding sites was 20-fold less than in the brain. In culture, melatonin inhibited pituitary cAMP accumulation induced by forskolin, the adenyl cyclase stimulator. Forskolin also induced an increase in GH release, which was reduced in the presence of picomolar concentrations of melatonin. At higher concentrations, the effects of melatonin became stimulatory. In the absence of forskolin, melatonin induced a dose-dependent increase in GH release, and a dose-dependent decrease in PRL release. Melatonin effects were abolished upon addition of luzindole, a melatonin antagonist. Our results provide the first evidence that melatonin modulates GH and PRL secretion in Teleost fish pituitary. Melatonin effects on GH have never been reported in any vertebrate before. The effects result from a direct action of melatonin on pituitary cells. The complexity of the observed responses suggests several types of melatonin receptors might be involved.
International audienceThe red drum Sciaenops ocellatus is an estuarine-dependent sciaenid that has supported important recreational and commercial fisheries for many years. Since the 1980s, this species has been farmed in different regions of the world and studies have been conducted to find natural ways to improve its culture. Sciaenops ocellatus is well known for making calls but studies on this characteristic have been mainly restricted to passive acoustics. The aim of this study was to provide acoustic-related information that could be useful in rearing practices. We have studied in detail fish calling characteristics, described their sound-producing mechanism and tested the recordings in different kinds of confinements (floating cages, concrete and fibreglass tanks). Contrary to previous studies, calls were recorded mainly in the morning, between 06:00 and 09:00. Sounds are made only by males; females do not have sound-producing apparatus. The anatomy, muscle ultrastructure data and calling characteristics show conclusively that calls result from the contraction of high speed muscles which are characterized by the very small diameter (7 μm) of the muscle cells. Preliminary results suggest that sound characteristics can give information on the fish physiology but further studies are needed. The effects of resonance of fibreglass tanks are experimentally highlighted, showing unequivocally that all the characteristics of fish calls are completely distorted, even in big tanks (13 m3). These findings should be taken into account when using pre-recorded sounds in the rearing of this species because it can affect communication during courtship activity
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