Abstract:Fish are commonly sedated to render them immobile and thus easier to handle for research, veterinary, and aquaculture practices. Since sedation itself imposes a significant challenge on the targeted fish, the selection of sedation methods that minimize physiological and behavioral disturbance and recovery time is essential. Two popular sedation methods include the chemical tricaine methanesulfonate (MS‐222) and electrosedation. Although many studies have already investigated the physiological consequences of t… Show more
“…However, Largemouth Bass that were exposed to FHGs and the PES had significantly lower opercular rates than those in the control treatment during simulated surgery ( Figure 2B); after treatment, their opercular rates increased toward the rate observed in the control group. Similar to the findings of Trushenski et al (2012b) and Prystay et al (2017), suppressed opercular rates associated with electrosedation were relatively shortlived once the fish were removed from sedation and their nervous system was able to recover.…”
Section: Opercular Rates and Exhaustive Chase Responsessupporting
confidence: 74%
“…() and Prystay et al. (), suppressed opercular rates associated with electrosedation were relatively short‐lived once the fish were removed from sedation and their nervous system was able to recover.…”
Fish sedation facilitates safer handling of fish during scientific research or fisheries assessment practices, thus limiting risk of injury to fish and reducing stress responses. In recent years, there has been growing interest in using electricity to sedate fish; two methods include (1) lower‐voltage, non‐pulsed‐DC fish handling gloves (FHGs) that tend to only sedate fish while the gloves are touching the animal; and (2) a comparatively high‐voltage, pulsed‐DC Portable Electrosedation System (PES) that leads to galvanonarcosis. This study compared the physiological consequences of exposure to FHGs and PES in teleost fish. Bluegills Lepomis macrochirus and Largemouth Bass Micropterus salmoides were exposed to FHGs, PES, or a handling control for a 3‐min simulated surgery. Blood was then sampled at 0.5 and 4.5 h postexposure and was analyzed for blood glucose, blood lactate, and plasma cortisol concentrations. Opercular rates were monitored during surgery, at 2 min postsurgery, and 0.5 h postsurgery. At 24 h postsurgery, time to exhaustion (via a standardized swimming chase protocol) was assessed. Fish exposed to FHGs tended to exhibit lower opercular rates than fish that were sedated with the PES during simulated surgery. Cortisol levels of Largemouth Bass treated with FHGs were higher than those of fish sedated with the PES. Glucose levels recorded for Bluegills at 4.5 h postsurgery were higher with FHGs than with the PES. In both species, lactate was lower for fish treated with FHGs than for those treated with the PES. At 24 h posttreatment, Bluegills sedated with FHGs exhibited a longer time to exhaustion than those subjected to the PES, whereas Largemouth Bass sedated with the PES exhibited a longer time to exhaustion than those sedated with FHGs. Physiological responses to treatments were inconsistent between species. Further investigation to determine the optimal electrosedation method is required.
“…However, Largemouth Bass that were exposed to FHGs and the PES had significantly lower opercular rates than those in the control treatment during simulated surgery ( Figure 2B); after treatment, their opercular rates increased toward the rate observed in the control group. Similar to the findings of Trushenski et al (2012b) and Prystay et al (2017), suppressed opercular rates associated with electrosedation were relatively shortlived once the fish were removed from sedation and their nervous system was able to recover.…”
Section: Opercular Rates and Exhaustive Chase Responsessupporting
confidence: 74%
“…() and Prystay et al. (), suppressed opercular rates associated with electrosedation were relatively short‐lived once the fish were removed from sedation and their nervous system was able to recover.…”
Fish sedation facilitates safer handling of fish during scientific research or fisheries assessment practices, thus limiting risk of injury to fish and reducing stress responses. In recent years, there has been growing interest in using electricity to sedate fish; two methods include (1) lower‐voltage, non‐pulsed‐DC fish handling gloves (FHGs) that tend to only sedate fish while the gloves are touching the animal; and (2) a comparatively high‐voltage, pulsed‐DC Portable Electrosedation System (PES) that leads to galvanonarcosis. This study compared the physiological consequences of exposure to FHGs and PES in teleost fish. Bluegills Lepomis macrochirus and Largemouth Bass Micropterus salmoides were exposed to FHGs, PES, or a handling control for a 3‐min simulated surgery. Blood was then sampled at 0.5 and 4.5 h postexposure and was analyzed for blood glucose, blood lactate, and plasma cortisol concentrations. Opercular rates were monitored during surgery, at 2 min postsurgery, and 0.5 h postsurgery. At 24 h postsurgery, time to exhaustion (via a standardized swimming chase protocol) was assessed. Fish exposed to FHGs tended to exhibit lower opercular rates than fish that were sedated with the PES during simulated surgery. Cortisol levels of Largemouth Bass treated with FHGs were higher than those of fish sedated with the PES. Glucose levels recorded for Bluegills at 4.5 h postsurgery were higher with FHGs than with the PES. In both species, lactate was lower for fish treated with FHGs than for those treated with the PES. At 24 h posttreatment, Bluegills sedated with FHGs exhibited a longer time to exhaustion than those subjected to the PES, whereas Largemouth Bass sedated with the PES exhibited a longer time to exhaustion than those sedated with FHGs. Physiological responses to treatments were inconsistent between species. Further investigation to determine the optimal electrosedation method is required.
“…Finally, long recovery durations associated with the use of many sedation agents (Trushenski et al, 2013) can be a significant issue for the live release of fish back into the wild. Any lingering effects of the sedation agent may contribute to alterations in natural behaviour (Losey & Hugie, 1994;Mettam et al, 2011;Prystay et al, 2017) or lead to postrelease predation (reviewed in Raby et al, 2014). Lingering effects would be suboptimal for studies in which post-release behaviour is monitored (i.e., telemetry studies; see Brownscombe et al, 2019) g., Chatakondi & Kelly, 2019;Nguyen et al, 2018;Rucinque et al, 2018;Trushenski et al, 2017).…”
Section: Many Of the Anaesthesia Methods Discussed May Extend Captivitymentioning
confidence: 99%
“…Appropriately, many anaesthetics have strict legal requirements on their use and disposal (reviewed in Trushenski et al ., 2013), meaning using anaesthetics in remote environments and field applications is difficult given the numerous legal and logistical challenges of chemical anaesthetics. Chemical anaesthetics in field settings are not recommended and, as an alternative, the use of low‐voltage electricity is suggested [either as electric gloves (Abrams et al ., 2018) or as a portable electrosedation system unit (Prystay et al ., 2017)]. Low‐voltage electricity has been proposed as an anaesthetic to aid in fish restraint because of relatively short recovery times after exposure ( i.e ., seconds; Vandergoot et al ., 2011; Trushenski & Bowker, 2012; Ward et al ., 2017; Abrams et al ., 2018; Reid et al ., 2019).…”
Section: The Use Of Anaesthesia In Caudal Puncturementioning
Blood sampling through the caudal vasculature is a widely used technique in fish biology for investigating organismal health and physiology. In live fishes, it can provide a quick, easy and relatively non-invasive method for obtaining a blood sample (cf. cannulation and cardiac puncture). Here, a general set of recommendations are provided for optimizing the blood sampling protocol that reflects best practices in animal welfare and sample integrity. This includes selecting appropriate use of anaesthetics for blood sampling as well as restraint techniques for situations where sedation is not used. In addition, ideal sampling environments where the fish can freely ventilate and strategies for minimizing handling time are discussed. This study summarizes the techniques used for extracting blood from the caudal vasculature in live fishes, highlighting the phlebotomy itself, the timing of sampling events and acceptable blood sample volumes. This study further discuss considerations for selecting appropriate physiological metrics when sampling in the caudal region and the potential benefits that this technique provides with respect to long-term biological assessments. Although general guidelines for blood sampling are provided here, it should be recognized that contextual considerations (e.g., taxonomic diversity, legal matters, environmental constraints) may influence the approach to blood sampling. Overall, it can be concluded that when done properly, blood sampling live fishes through the caudal vasculature is quick, efficient and minimally invasive, thus promoting conditions where live release of focal animals is possible.
“…The stimulus device consisted of a long plastic rod that was tipped with a novel object (a brightly colored orange and yellow fishing float). This float was comparable in size and color to those that were used in prior works (a simple orange ball) as a standardized means of conducting an FID trial (see Kim et al 2009;Elvidge et al 2013;Cooke et al 2017;Prystay et al 2017). This is a well-established methodological approach for conducting an FID trial.…”
In recreational fisheries it is understood that individual fish that exhibit bolder personality traits have a tendency to be removed from the population (i.e., fishing mortality via harvest or catch‐and‐release mortality), while more timid individuals remain. The use of aquatic protected areas (APAs) has been promoted as a means of offsetting the negative consequences that are associated with fishing mortality by protecting the full suite of phenotypes. However, little work has investigated whether APAs are able to maintain heterogeneity in behavioral traits in wild fish. We attempted to address this question by using wild Bluegill Lepomis macrochirus from Lake Opinicon, a freshwater system consisting of both an APA and heavily fished areas. The Bluegill were obtained via angling from three zones in the lake: the main lake area (i.e., fished), the APA (which has been in place since the 1940s), and a transitional zone between these two areas. In the laboratory, the Bluegill were subjected to two behavioral assessments, a Z‐maze and a flight‐initiation‐distance (FID) test, to address differences in boldness and risk‐taking between these populations. No significant effects of capture zone were detected for any of the behavioral metrics that were assessed in the maze trial. However, individuals that originated from the main lake population had significantly higher FID scores than the fish from the transitional zone and the APA did, indicating that they were more timid. Our results suggest that fisheries activities may only be acting only on specific traits, which may explain some of the null results that are presented here. Nevertheless, our study provides evidence that APAs are providing a reservoir of less timid individuals, which is consistent with an evolutionarily enlightened management strategy.
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