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The unique engulfment filtration strategy of microphagous rorqual whales has evolved relatively recently (

Using social groups (i.e. schools) of the tropical damselfish Chromis viridis, we test how familiarity through repeated social interactions influences fast-start responses, the primary defensive behaviour in a range of taxa, including fish, sharks, and larval amphibians. We focus on reactivity through response latency and kinematic performance (i.e. agility and propulsion) following a simulated predator attack, while distinguishing between first and subsequent responders (direct response to stimulation versus response triggered by integrated direct and social stimulation, respectively). In familiar schools, first and subsequent responders exhibit shorter latency than unfamiliar individuals, demonstrating that familiarity increases reactivity to direct and, potentially, social stimulation. Further, familiarity modulates kinematic performance in subsequent responders, demonstrated by increased agility and propulsion. These findings demonstrate that the benefits of social recognition and memory may enhance individual fitness through greater survival of predator attacks., Nadler et al examined how social familiarity influences fast-start defensive responses in the tropical damselfish Chromis viridis. They showed that fish in familiar schools responded faster to threats and the behaviour of others in the school than those in unfamiliar schools, which indicates that social recognition and memory can modify fish anti-predator behaviour.

This study investigated the oxygen consumption of the putative oxygen conformer marbled swamp eel Synbranchus marmoratus during progressive hypoxia. Earlier studies have not reached agreement on whether S. marmoratus is a conformer or regulator. Our results support the view that S. marmoratus is an oxygen regulator, like most bony fishes.

Fast escape responses to a predator threat are fundamental to the survival of mobile marine organisms. However, elasmobranchs are often underrepresented in such studies. Here, we measured the escape latency (time interval between the stimulus and first visible reaction) of mechanically induced escape responses in the Pacific spiny dogfish, Squalus suckleyi, and in two teleosts from the same region, the great sculpin, Myoxocephalus polyacanthocephalus, and the pile perch, Rhacochilus vacca. We found that the dogfish had a longer minimum latency (66.7 ms) compared with that for the great sculpin (20.8 ms) and pile perch (16.7 ms). Furthermore, the dogfish had a longer latency than that of 48 different teleosts identified from 35 different studies. We suggest such long latencies in dogfish may be due to the absence of Mauthner cells, the giant neurons that control fast escape responses in fishes.

© 2020. Published by The Company of Biologists Ltd. Billfishes are well known for their distinctive elongated rostra, i.e. bills. The functional significance of billfish rostra has been frequently discussed and the recent discovery of an oil gland (glandula oleofera) at the base of the rostrum in swordfish, Xiphias gladius, has added an interesting facet to this discussion regarding the potential co-evolution of gland and rostra. Here, we investigated the oil gland and oil pores (through which the oil is brought to the skin surface) of four billfish species - swordfish, Atlantic blue marlin (Makaira nigricans), Indo-Pacific sailfish (Istiophorus platypterus) and striped marlin (Kajikia audax) - and provide detailed evidence for the presence of an oil gland in the last three. All four species had a high density of oil pores on the forehead which is consistent with the hypothesis of hydrodynamic benefits of the oil. The extension of the pores onto the front half of the rostrum in sailfish and striped marlin, but not in swordfish or blue marlin, suggests that the oil may have additional functions. One such function could be linked to the antibacterial and anti-inflammatory properties of the oil. However, the available evidence on predatory rostrum use (and hence the likelihood of tissue damage) is only partly consistent with the extension of pores on rostra across species. We conclude that the oil gland probably serves multiple, non-mutually exclusive functions. More detailed information on rostrum use in blue marlin and swordfish is needed to better link behavioural and morphological data with the aim of accomplishing a full comparative analysis.

Wave-induced surge conditions are found in shallow marine ecosystems worldwide; yet, few studies have quantified how cyclical surges may affect free swimming animals. Here, we used a recently adapted respirometry technique to compare the energetic costs of a temperate fish species (Cymatogaster aggregata) swimming against a steady flow versus cyclical unidirectional and bidirectional surges in which unsteady swimming (such as accelerating, decelerating and turning) occurs. Using oxygen uptake (ṀO2) as an estimate of energetic costs, our results reveal that fish swimming in an unsteady (i.e. cyclical) unidirectional flow showed no clear increase in costs when compared to a steady flow of the same average speed, suggesting that costs and savings from cyclical acceleration and coasting are near equal. Conversely, swimming in a bidirectional cyclical flow incurred significantly higher energetic costs relative to a steady, constant flow, likely due to the added cost of turning around to face the changing flow direction. On average, we observed a 50% increase in ṀO2 of fish station holding within the bidirectional flow (227.8 mg O2 kg−1 h−1) compared to a steady, constant flow (136.1 mg O2 kg−1 h−1) of the same mean velocity. Given wave-driven surge zones are prime fish habitats in the wild, we suggest the additional costs fish incur by station holding in a bidirectional cyclical flow must be offset by favourable conditions for foraging and reproduction. With current and future increases in abiotic stressors associated with climate change, we highlight the importance of incorporating additional costs associated with swimming in cyclical water flow in the construction of energy budgets for species living in dynamic, coastal habitats.

Linking morphological differences in foraging adaptations to prey choice and feeding strategies has provided major evolutionary insights across taxa. Here, we combine behavioural and morphological approaches to explore and compare the role of the rostrum (bill) and micro-teeth in the feeding behaviour of sailfish ( Istiophorus platypterus ) and striped marlin ( Kajikia audax ) when attacking schooling sardine prey. Behavioural results from high-speed videos showed that sailfish and striped marlin both regularly made rostrum contact with prey but displayed distinct strategies. Marlin used high-speed dashes, breaking schools apart, often contacting prey incidentally or tapping at isolated prey with their rostra; while sailfish used their rostra more frequently and tended to use a slower, less disruptive approach with more horizontal rostral slashes on cohesive prey schools. Capture success per attack was similar between species, but striped marlin had higher capture rates per minute. The rostra of both species are covered with micro-teeth, and micro-CT imaging showed that species did not differ in average micro-tooth length, but sailfish had a higher density of micro-teeth on the dorsal and ventral sides of their rostra and a higher amount of micro-teeth regrowth, suggesting a greater amount of rostrum use is associated with more investment in micro-teeth. Our analysis shows that the rostra of billfish are used in distinct ways and we discuss our results in the broader context of relationships between morphological and behavioural feeding adaptations across species.

Environmental factors add constraints to organismal performance at their extremes, but support optimal performance at energetically beneficial conditions. In aquatic environments , salinity adds costs for ion transportation to the energetic budgets of osmoregulating animals, such as teleost fishes. These additional costs may limit the available energy for important ecological traits of fishes, including maximal and optimal swimming performance, which are required for successful foraging and migration in the wild. Here, we hypothesize that swimming performance, and its related costs, will be optimized at near-isoosmotic salinity, and decline under more saline conditions. Using the euryhaline shiner perch ( Cymatogaster aggregata) as a model for coastal fishes, we determined critical swimming speeds and oxygen consumption rates during swimming at salinities of 12 g kg−1 (near-isoosmotic, brackish, S12) and 31 g kg−1 (hyperosmotic, marine, S31). Most tested metrics were unaffected by salinity, including aerobic scope, active metabolic rate and optimal swimming speed. Likewise, critical swimming speed (in body lengths per second, BL s−1) was not significantly different between fishes acclimated to S12 (4.8 ± 0.6 BL s−1) or S31 (5.1 ± 0.5 BL s−1, means ± SD, n = 5) suggesting that the fish could swim and hunt for prey equally well regardless of salinity. However, S31 conditions did cause comparatively higher oxygen consumption rates at swimming speeds from 0.5 to 1.5 BL s−1 , and a 20% increase in the extrapolated standard metabolic rate (i.e. cost of maintaining bodily functions). Our results confirm that there is an added energetic cost of salinity, but highlight that the cost of osmoregulation appears minimal relative to the energetic demands of swimming, and consequently has no effect on the maximal swimming performance of adult shiner perch. Given the strong salinity gradients naturally encountered in many coastal ecosystems, these data provide an explanation for the capacity of a coastal roaming species to move in an out of coastal habitat zones without significantly compromising their ability to hunt prey, avoid predation and migrate. As climate change locally affects environmental salinity, our results offer valuable insight towards the effects of environmental perturbations on fishes in coastal marine and estuarine habitats.

When oil spills occur, behavior is the first line of defense for a fish to avoid being contaminated. We determined the avoidance threshold of the European seabass (Dicentrarchus labrax) to the water-soluble fraction (WSF) of oil using a dual-flow choice box. The results showed that a plume of 20%-diluted WSF (total polycyclic aromatic hydrocarbon [PAH] concentration: 8.54 μg L-1 ) triggered a significant avoidance response that was detected within 7.5 min of introducing WSF-contaminated water into the experimental setup. However, the ecological relevance of seabass capacity to detect and avoid WSF remains to be established. In the short term, such a response is indeed liable to reduce seabass contact time with oil-contaminated water and thus preserve their functional integrity. In the long term, however, avoidance may contribute to the displacement of a population into a possibly less auspicious environment, with consequences very similar to those of contaminant exposure, that is, disturbed population dynamics and demography. Environ Toxicol Chem 2018;37:854-859. © 2017 SETAC.

The effect of the presence and angular position of a refuge on the direction and kinematics of mechanically-induced escape responses was observed in staghorn sculpins Leptocottus armatus using high-speed video. The results showed that the angular position of the refuge did not affect locomotor performance (speed and acceleration), although it did affect the escape trajectories. Therefore, the angular position of a refuge can modulate the direction taken by the L. armatus during the early stages of their escape response and this response can be affected by both repulsive (i.e. threats) and attractive (i.e. refuges) points of reference.

Recent work has shown that the behaviour of marine organisms can be affected by elevated PCO2, although little is known about the effect of multiple stressors. We therefore investigated the effect of elevated PCO2 and temperature on locomotion and behaviour during prey searching in the marine gastropod Concholepas concholepas, a predator characteristic of the southeastern Pacific coast. Movement duration, decision time, route finding and lateralization were measured using a T-maze tank with a prey positioned behind a barrier. Four treatments, representing present day and near-future scenarios of ocean acidification and warming were used in rearing the individuals for 6 months. Regardless of the treatment, no significant differences were found in relative and absolute lateralization before and after exposure for 6 months. However, relative lateralization was not repeatable for animals tested after 6 months at elevated PCO2 at both experimental temperatures, whereas it was repeatable in individuals kept at the present day level of PCO2. We suggest that these effects may be related to a behavioural malfunction caused by elevated PCO2. Movement duration, decision time and route finding were not repeatable. However, movement duration and decision time increased and route finding decreased in elevated PCO2 (at 15°C), suggesting that elevated PCO2 has negative effects on the locomotor and sensory performance of C. concholepas in the presence of a prey odour, thereby decreasing their ability to forage efficiently.

Sea urchin harvesting has rapidly expanded in the last decades. Since many sea urchin species play important ecological role, large-scale commercial sea urchin fisheries can have complex effects on benthic communities. In many temperate regions, overharvesting has compromised marine ecosystems to such an extent that reintroduction of sea urchins raised in captivity may be a valid solution for the enhancement of depleted marine wild populations. In some regions of the Mediterranean Sea, improving the growth efficiency of captive sea urchin Paracentrotus lividus to be reintroduced has become a widespread practice. However, no study has yet considered the potential behavioural effects of raising sea urchins in captivity when they are introduced in the natural environment. This study provides information about the behavioural effects of captivity on P. lividus in terms of locomotion performance, a trait that can be fundamental for responding to predators and for relocation after environmental disturbances such as currents and waves. Movements of captive-born and wild sea urchins were video-recorded and compared in (i) total exposure to external cues, (ii) partial exposure to external cues and (iii) absence of external cues. Latency of locomotion, average speed and average velocity of sea urchins showed significant differences with respect to the level of exposure and their origin (i.e. wild vs. captive-born). Our results demonstrate that captive-born sea urchins in the wild showed long latency and slower locomotor performance when compared to wild sea urchins. Conversely, the straightness-of-path and locomotion direction of captive-born and wild sea urchins were similar in natural settings. Our results therefore suggest that captive-born sea urchins suffer the negative effects of captivity when introduced in a natural environment. Understanding the factors that decrease the performance of sea urchin will be important for developing procedures aimed at minimizing the negative effect of captivity before release into the wild.

Striped seagrass meadows are formed by narrow ribbons which are elevated over the seabed and separated by channels. Limited information on the genesis and development of this morphological pattern, including the adaptive responses of associated biota, is preventing holistic insight into the functioning of such protected ecosystems. This paper assessed the structural dynamics of a Posidonia oceanica striped meadow and the distribution and 3D orientation of the associated bivalve Pinna nobilis. Our analysis of the interaction between bedforms, bottom currents, and the distribution of P. nobilis revealed that the striped seascape is the result of a self-organisation process driven by feedback interactions among seagrass growth, sediment deposition, and hydrodynamics. The results suggest that the ribbon wall is the most suitable sub-habitat for this species, because it supports the highest density of P. nobilis, compared to the meadow top and bottom. Here, specimens can take advantage of the resuspension induced by hydrodynamics and open their shells towards the current, thus enhancing food intake. Therefore, our results show that self-organisation in striped seagrass meadow affects the distributional pattern of P. nobilis, providing new insights into the autoecology of this species beyond the conservation implications for its habitat.

The ecological and economic importance of fish act as a brake on the development of chemical dispersants as operational instruments following oil spills. Although a valuable and consistent body of knowledge exists, its use in spill response is limited. The objective of the present study was to increase current knowledge base to facilitate the translation of published data into information of operational value. Thus we investigated the dose-response relationship between dispersant-treated oil exposure and ecologically relevant consequences by combining laboratory and field experiments. Effects were examined over almost a year using juveniles of the slowly growing, commercially important European sea bass (Dicentrarchus labrax). A reliable interpretation of biomarker responses requires a complete knowledge of the factors likely to affect them. Interpopulational variability is of particular importance in environmental impact assessment because biomarker responses from a population collected in an impacted area are classically compared with those collected in a clean site. Our study revealed no effect of the exposure to dispersant-treated oil on fish hypoxia tolerance and temperature susceptibility at 1 and 11 mo post exposure. Similarly, no effect of the exposure was observed on the ability of the fish to cope with environmental contingencies in the field, regardless of the dose tested. Thus we feel confident to suggest that a 48-h exposure to chemically treated oil does not affect the ability of sea bass to cope with mild environmental contingencies. Finally, investigation of interpopulation variability revealed large differences in both hypoxia tolerance and temperature susceptibility among the 2 populations tested, suggesting that this variability may blur the interpretation of population comparisons as classically practiced in impact assessment. Environ Toxicol Chem 2019;38:210-221. © 2018 SETAC.

Billfishes are considered to be among the fastest swimmers in the oceans. Previous studies have estimated maximum speed of sailfish and black marlin at around 35 m s−1 but theoretical work on cavitation predicts that such extreme speed is unlikely. Here we investigated maximum speed of sailfish, and three other large marine pelagic predatory fish species, by measuring the twitch contraction time of anaerobic swimming muscle. The highest estimated maximum swimming speeds were found in sailfish (8.3±1.4 m s−1), followed by barracuda (6.2±1.0 m s−1), little tunny (5.6±0.2 m s−1) and dorado (4.0±0.9 m s−1); although size-corrected performance was highest in little tunny and lowest in sailfish. Contrary to previously reported estimates, our results suggest that sailfish are incapable of exceeding swimming speeds of 10-15 m s−1, which corresponds to the speed at which cavitation is predicted to occur, with destructive consequences for fin tissues., Summary: Using muscle contraction measurements, this work provides evidence that sailfish are most likely unable to reach the extremely high speeds claimed by previous research and popular articles.

This study compares the critical oxygen saturation (O2 crit ) levels of the shiner perch Cymatogaster aggregata obtained using two different methods wherein hypoxia is induced either by the fish's respiration (closed respirometry) or by degassing oxygen with nitrogen (intermittent-flow respirometry). Fish exhibited loss of equilibrium at a higher O2 saturation in the closed respirometry method when compared with the intermittent-flow method. Utilization of closed respirometry yielded O2 crit measurements that were almost twice as high as those obtained with intermittent-flow respirometry. The lower hypoxia tolerance in closed respirometry is consistent with additional stress, caused by a build-up of ammonia and carbon dioxide and a faster rate in dissolved oxygen decline. The results indicate that these two methods of determining hypoxia tolerance in aquatic organisms are not comparable, and that much care should be given to method choice.

Hypoxia and petrogenic hydrocarbon contamination are two anthropogenic stressors that coexist in coastal environments. Although studies have estimated the impact of each stressor separately, few investigations have assessed the effects of these stressors in interaction. We therefore investigated the impact of these combined stressors on sea bass, (Dicentrarchus labrax) physiology. After experimental contamination with physically dispersed oil, fish were exposed to hypoxia or normoxia, and active/standard metabolic rates (AMR and SMR, respectively), and metabolic scope (MS) were estimated. At the protocol's end, the uptake of polycyclic aromatic hydrocarbons (PAHs) was estimated by evaluating relative concentrations of bile metabolites. In terms of bile metabolites, our results validated the uptake of PAHs by contaminated fish in our experimental settings, and further suggest that the hypoxic period after contamination does not reduce or increase compound metabolization processes. Our data showed significant effects of hypoxia on all metabolic rates: a significant drastic AMR reduction and significant SMR diminution led to decreased MS. We also found that oil contamination significantly impacted AMR and MS, but not SMR. These results suggested that when evaluated separately, hypoxia or oil affect the metabolic rate of sea bass. On the other hand, when evaluated in combination, no cumulative effects were observed, since fish exposed to both stressors did not show a stronger impact on metabolism than fish exposed to hypoxia alone. This suggests that oil impacts fish metabolism when fish occupy normoxic waters, and that oil does not magnify hypoxia-induced effects on fish metabolism.

We evaluated the effects of projected, near future ocean acidification (OA) and extreme events of temperature (warming or cooling) on the thermal tolerance of Concholepas concholepas, a coastal benthic keystone species. Three separate trials of an experiment were conducted by exposing juvenile C. concholepas for 1 month to one of two contrasting pCO2 levels (~500 and ~1200 μatm). In addition, each pCO2 level was combined with one of four temperature treatments. The control was 15 °C, whilst the other temperatures were 10 °C (Trial 1), 20 °C (Trial 2) and 25 °C (Trial 3). At the end of each trial, we assessed Critical Thermal maximum (CTmax) and minimum (CTmin) via self-righting success, calculated partial thermal tolerance polygons, measured somatic growth, determined transcription of Heat Shock Proteins 70 (HSP70) and measured oxygen consumption rates. Regardless of pCO2 level, HSP70 transcript levels were significantly higher in juveniles after exposure to extreme temperatures (10 °C and 25 °C) indicating physiological stress. Oxygen consumption rates increased with increasing temperature from 10 °C to 20 °C though showed a decrease at 25 °C. This rate was not affected by pCO2 or the interaction between temperature and pCO2. Juveniles exposed to present-day and near future pCO2 levels at 20 °C showed similar thermal tolerance polygonal areas; whilst changes in both CTmin and CTmax at 25 °C and 10 °C caused narrower and broader areas, respectively. Temperature affected growth, oxygen consumption and HSP70 transcription in small juvenile C. concholepas. Exposure to elevated pCO2 did not affect thermal tolerance, growth or oxygen consumption at temperatures within the thermal range normally experienced by this species in northern Chile (15-20 °C). At elevated pCO2 conditions, however, exposure to warmer (25 °C) or colder (10 °C) temperatures reduced or increased the thermal area, respectively. This study demonstrates the importance of examining the thermal-tolerance edges to better understand how OA and temperature will combine to physiologically challenge inter-tidal organisms.

Hydrocarbons contamination and hypoxia are two stressors that can coexist in coastal ecosystems. At present, few studies evaluated the combined impact of these stressors on fish physiology and behavior. Here, we tested the effect of the combination of hypoxia and petrogenic hydrocarbons on the anti-predator locomotor performance of fish. Specifically, two groups of European sea bass (Dicentrarchus labrax) were exposed to clean water (Ctrl) or oil-contaminated water (Oil). Subsequently, fish of both groups were placed in normoxic (norx) or hypoxic (hyp) experimental tanks (i.e. four groups of fish were formed: Ctrl norx, Ctrl hyp, Oil norx, Oil hyp). In these tanks, escape response 2 was elicited by a mechano-acoustic stimulus and recorded with a high speed camera. Several variables were analyzed: escape response duration, responsiveness (percentage of fish responding to the stimulation), latency (time taken by the fish to initiate a response), directionality (defined as away or toward the stimulus), distance-time variables (such as speed and acceleration), maneuverability variables (such as turning rate), escape trajectory (angle of flight) and distancing of the fish from the stimulus. Results revealed (i) effects of stressors (Ctrl hyp, Oil norx and Oil hyp) on the directionality; (ii) effects of Oil norx and Oil hyp on maneuverability and (iii) effects of Oil hyp on distancing. These results suggest that individual stressors could alter the escape response of fish and that their combination could strengthen these effects. Such an impact could decrease the probability of prey escape success. By investigating the effects of hydrocarbons (and the interaction with hypoxia) on the anti-predator behavior of fish, this work increases our understanding of the biological impact of oil spill. Additionally, the results of this study are of interest for oil spill impact evaluation and also for developing new ecotoxicological tools of ecological significance.

Animals are exposed to variable and rapidly changing environmental flow conditions, such as wind in terrestrial habitats and currents in aquatic systems. For fishes, previous work suggests that individuals exhibit flow-induced changes in aerobic swimming performance. Yet, no one has examined whether similar plasticity is found in fast-start escape responses, which are modulated by anaerobic swimming performance, sensory stimuli and neural control. In this study, we used fish from wild schools of the tropical damselfish Chromis viridis from shallow reefs surrounding Lizard Island in the Great Barrier Reef, Australia. The flow regime at each site was measured to ascertain differences in mean water flow speed and its temporal variability. Swimming and escape behaviour in fish schools were video-recorded in a laminar-flow swim tunnel. Though each school's swimming behaviour (i.e. alignment and cohesion) was not associated with local flow conditions, traits linked with fast-start performance (particularly turning rate and the distance travelled with the response) were significantly greater in individuals from high-flow habitats. This stronger performance may occur due to a number of mechanisms, such as an in situ training effect or greater selection pressure for faster performance phenotypes in areas with high flow speed. This article has an associated First Person interview with the first author of the paper., Summary: Fish exhibit flow-induced changes in their fast-start escape performance, likely due to an in situ training effect and/or selection for faster performance phenotypes in areas with high flow speed.

Fish swimming energetics are often measured in laboratory environments which attempt to minimize turbulence, though turbulent flows are common in the natural environment. To test whether the swimming energetics and kinematics of shiner perch Cymatogaster aggregata (a labriform swimmer) were affected by turbulence, two flow conditions were constructed in a swim-tunnel respirometer. A low-turbulence flow was created using a common swim-tunnel respirometry setup with a flow straightener and fine-mesh grid to minimize velocity fluctuations. A high-turbulence flow condition was created by allowing large velocity fluctuations to persist without a flow straightener or fine grid. The two conditions were tested with Particle Image Velocimetry to confirm significantly different turbulence properties throughout a range of mean flow speeds. Oxygen consumption rates of the swimming fish increased with swimming speeds and pectoral fin beat frequencies in both flow conditions. Higher turbulence also caused a greater positional variability in swimming individuals (vs. low-turbulence flow) at medium and high speeds. Surprisingly, fish used less oxygen in high turbulence compared to low-turbulence flow at medium and high swimming speeds. Simultaneous measurements of swimming kinematics indicated that these reductions in oxygen consumption could not be explained by specific known flow-adaptive behaviours such as Kármán-gaiting or entraining. Therefore, fish in high-turbulence flow may take advantage of the high variability in turbulent energy through time. These results suggest that swimming behavior and energetics measured in the lab in straightened flow, typical of standard swimming respirometers, might differ from that of more turbulent, semi-natural flow conditions. Postprint

Billfishes are considered among the fastest swimmers in the oceans. Despite early estimates of extremely high speeds, more recent work showed that these predators (e.g., blue marlin) spend most of their time swimming slowly, rarely exceeding 2 m s(-1). Predator-prey interactions provide a context within which one may expect maximal speeds both by predators and prey. Beyond speed, however, an important component determining the outcome of predator-prey encounters is unsteady swimming (i.e., turning and accelerating). Although large predators are faster than their small prey, the latter show higher performance in unsteady swimming. To contrast the evading behaviors of their highly maneuverable prey, sailfish and other large aquatic predators possess morphological adaptations, such as elongated bills, which can be moved more rapidly than the whole body itself, facilitating capture of the prey. Therefore, it is an open question whether such supposedly very fast swimmers do use high-speed bursts when feeding on evasive prey, in addition to using their bill for slashing prey. Here, we measured the swimming behavior of sailfish by using high-frequency accelerometry and high-speed video observations during predator-prey interactions. These measurements allowed analyses of tail beat frequencies to estimate swimming speeds. Our results suggest that sailfish burst at speeds of about 7 m s(-1) and do not exceed swimming speeds of 10 m s(-1) during predator-prey interactions. These speeds are much lower than previous estimates. In addition, the oscillations of the bill during swimming with, and without, extension of the dorsal fin (i.e., the sail) were measured. We suggest that extension of the dorsal fin may allow sailfish to improve the control of the bill and minimize its yaw, hence preventing disturbance of the prey. Therefore, sailfish, like other large predators, may rely mainly on accuracy of movement and the use of the extensions of their bodies, rather than resorting to top speeds when hunting evasive prey.

Lateralization is widespread throughout the animal kingdom [1; 2; 3; 4; 5; 6 ; 7] and can increase task efficiency via shortening reaction times and saving on neural tissue [8; 9; 10; 11; 12; 13; 14; 15 ; 16]. However, lateralization might be costly because it increases predictability [17; 18; 19; 20 ; 21]. In predator-prey interactions, for example, predators might increase capture success because of specialization in a lateralized attack, but at the cost of increased predictability to their prey, constraining the evolution of lateralization. One unexplored mechanism for evading such costs is group hunting: this would allow individual-level specialization, while still allowing for group-level unpredictability. We investigated this mechanism in group hunting sailfish, Istiophorus platypterus, attacking schooling sardines, Sardinella aurita. During these attacks, sailfish alternate in attacking the prey using their elongated bills to slash or tap the prey [ 22; 23 ; 24]. This rapid bill movement is either leftward or rightward. Using behavioral observations of identifiable individual sailfish hunting in groups, we provide evidence for individual-level attack lateralization in sailfish. More strongly lateralized individuals had a higher capture success. Further evidence of lateralization comes from morphological analyses of sailfish bills that show strong evidence of one-sided micro-teeth abrasions. Finally, we show that attacks by single sailfish are indeed highly predictable, but predictability rapidly declines with increasing group size because of a lack of population-level lateralization. Our results present a novel benefit of group hunting: by alternating attacks, individual-level attack lateralization can evolve, without the negative consequences of individual-level predictability. More generally, our results suggest that group hunting in predators might provide more suitable conditions for the evolution of strategy diversity compared to solitary life.

We present evidence of a novel form of group hunting. Individual sailfish (Istiophorus platypterus) alternate attacks with other group members on their schooling prey (Sardinella aurita). While only 24% of attacks result in prey capture, multiple prey are injured in 95% of attacks, resulting in an increase of injured fish in the school with the number of attacks. How quickly prey are captured is positively correlated with the level of injury of the school, suggesting that hunters can benefit from other conspecifics' attacks on the prey. To explore this, we built a mathematical model capturing the dynamics of the hunt. We show that group hunting provides major efficiency gains (prey caught per unit time) for individuals in groups of up to 70 members. We also demonstrate that a free riding strategy, where some individuals wait until the prey are sufficiently injured before attacking, is only beneficial if the cost of attacking is high, and only then when waiting times are short. Our findings provide evidence that cooperative benefits can be realized through the facilitative effects of individuals' hunting actions without spatial coordination of attacks. Such ‘proto-cooperation’ may be the pre-cursor to more complex group-hunting strategies.

Pinna nobilis is the largest endemic bivalve of the Mediterranean Sea, declared protected since 1992. Although hydrodynamic stress induced by waves is known to influence density, size and orientation of P. nobilis , the effect of other hydrological features is unknown. This paper considers a P. nobilis population living within a Posidonia oceanica meadow in the Gulf of Oristano (Sardinia, Italy). We hypothesize that spatial differences in density and orientation of P. nobilis may be related to significant wave height (H S ), wave direction (D W ), bottom current direction (D BC ) and bottom current speed (S BC ). A population of P. nobilis was investigated at different sites and its distribution was correlated to hydrodynamics by means of a numerical modeling approach. The spatial distribution was patchy, with a density of 0.06–6.7 ind. 100 m − 2 . A non-uniform distribution of shell orientations (O S ) was demonstrated in 4 sites out of 6. D BC and S BC were the main factors affecting O S , while waves had little influence. A S BC of 0.07 m s − 1 appears to be the threshold for inducing specimen directionality with shells aligned to the current and the ventral side exposed to the flow. This suggests that feeding strategy is a key factor in determining O S , in addition to drag minimization. We also highlighted the role of adjacent lagoons in supporting high densities as a result of high food availability. These findings demonstrate the usefulness of modeling techniques in explaining the spatial distribution pattern of P. nobilis and in contributing to our knowledge of its ecological traits.

00000 ăWOS:000382802100022; International audience; Human alteration of marine ecosystems is substantial and growing. Yet, no adequate methodology exists that provides reliable predictions of how environmental degradation will affect these ecosystems at a relevant level of biological organization. The primary objective of this study was to develop a methodology to evaluate a fish's capacity to face a well-established environmental challenge, an exposure to chemically dispersed oil, and characterize the long-term consequences. Therefore, we applied high-throughput, non-lethal challenge tests to assess hypoxia tolerance, temperature susceptibility and maximal swimming speed as proxies for a fish's functional integrity. These whole animal challenge tests were implemented before (1 month) and after (1 month) juvenile European sea bass (Dicentrarchus labrax) had been acutely exposed (48 h) to a mixture containing 0.08 g L-1 of weathered Arabian light crude oil plus 4% dispersant (Corexit(C) EC9500A), a realistic exposure concentration during an oil spill. In addition, experimental populations were then transferred into semi-natural tidal mesocosm ponds and correlates of Darwinian fitness (growth and survival) were monitored over a period of 4 months. Our results revealed that fish acutely exposed to chemically dispersed oil remained impaired in terms of their hypoxia tolerance and swimming performance, but not in temperature susceptibility for 1 month post-exposure. Nevertheless, these functional impairments had no subsequent ecological consequences under mildly selective environmental conditions since growth and survival were not impacted during the mesocosm pond study. Furthermore, the earlier effects on fish performance were presumably temporary because re-testing the fish 10 months post-exposure revealed no significant residual effects on hypoxia tolerance, temperature susceptibility and maximal swimming speed. We propose that the functional proxies and correlates of Darwinian fitness used here provide a useful assessment tool for fish health in the marine environment.

We describe the BNH-Whale algorithm, which simulates a method of catching schooling fish employed by humpback whales called bubble net hunting. When this method is used, the fish are herded into a net of bubbles created by one or more whales. Modified flocking algorithms are used to guide whale and fish behaviour, with a relatively complex algorithm being used by the whales to trap and consume fish.

Eco-physiology studies, performed in laboratory under controlled conditions, provide an essential tool for quantifying the impact of environmental changes on the metabolism and behaviour of individual fish. One way of quantifying such impact is by measuring the Metabolic Scope (MS) of a fish and how it is affected by environmental factors. Laboratory experiments were performed to calculate the empirical mathematical equations describing the variation of the MS of flathead grey mullet, Mugil cephalus , under different environmental conditions (water temperature and water oxygen concentration). The equation obtained was introduced into a coupled hydrodynamic–ecological numerical model able to reproduce the variability of the water temperature, salinity, dissolved oxygen, and of the main dissolved nutrients and chlorophyll- a . The coupled empirical–numerical model was used to reproduce the temporal and spatial variation in MS of a M. cephalus fish population in the Oristano gulf and the Cabras lagoon system (Italy), a typical Mediterranean shallow water environment. Results from numerical simulations show that during the spring and the beginning of summer period, Cabras lagoon provides a higher MS for M. cephalus than the Oristano gulf. During the rest of the year, apart from some transitional phases, the gulf provides more suitable conditions (higher MS) for M. cephalus . The obtained results are in general accordance with fisheries data, showing that M. cephalus catches are highest during the end-July to August period, as they migrate out of the lagoon. This approach, combined with observation on the temporal and spatial distribution of fishes, can allow predictions of fish productivity in non-limiting conditions.

Schooling behavior in fish has been recognized to confer antipredator advantages. However, the mechanisms that lead to various patterns of escape maneuvers in fish schools are largely unknown. Here, we investigated the effect of startle stimulus characteristics (distance and orientation) on the escape maneuvers of schools of a highly gregarious fish species, the Atlantic herring Clupea harengus. We quantified information transfer of the onset of startle responses by analyzing the speed of the waves of their propagation ( Uw = 6.7 ± 1.6 m/s; mean ± SD). Uw was found to be positively correlated with the number of early responders (i.e., individuals reacting with a latency s). Lateral stimulation (30° < αs < 120°) elicits highly aligned maneuvers away from the stimulus, while frontal stimulations (αs < 30°) causes split maneuvers, which are followed by realignment about 1 s after stimulation. These simple rules suggest that certain stimulus characteristics are important factors determining the variability of antipredator maneuvers observable in schooling fish.

Made available in DSpace on 2022-04-28T19:04:23Z (GMT). No. of bitstreams: 0 Previous issue date: 2015-01-15 Fast-starts are brief accelerations commonly observed in fish within the context of predator-prey interactions. In typical C-start escape responses, fish react to a threatening stimulus by bending their body into a C-shape during the first muscle contraction (i.e. stage 1) which provides a sudden acceleration away from the stimulus. Recently, similar C-starts have been recorded in fish aiming at a prey. Little is known about C-starts outside the context of predator-prey interactions, though recent work has shown that escape response can also be induced by high temperature. Here, we test the hypothesis that air-breathing fish may use C-starts in the context of gulping air at the surface. Hoplosternum littorale is an airbreathing freshwater catfish found in South America. Field video observations reveal that their air-breathing behaviour consists of airgulping at the surface, followed by a fast turn which re-directs the fish towards the bottom. Using high-speed video in the laboratory, we compared the kinematics of the turn immediately following airgulping performed by H. littorale in normoxia with those of mechanically-triggered C-start escape responses and with routine (i.e. spontaneous) turns. Our results show that air-breathing events overlap considerably with escape responses with a large stage 1 angle in terms of turning rates, distance covered and the relationship between these rates. Therefore, these two behaviours can be considered kinematically comparable, suggesting that airbreathing in this species is followed by escape-like C-start motions, presumably to minimise time at the surface and exposure to avian predators. These findings show that C-starts can occur in a variety of contexts in which fish may need to get away from areas of potential danger. IAMC-CNR Oristano Loc. Sa Mardini Zoophysiology Department of Bioscience Aarhus University Department of Biological Sciences Indiana University South Bend ARC Centre of Excellence for Coral Reef Studies James Cook University School of Marine and Tropical Biology College of Marine and Environmental Sciences James Cook University DTU Aqua Section for Aquaculture Technical University of Denmark North Sea Research Centre, P.O. Box 101 Marine Biological Laboratory University of Copenhagen, Strandpromenaden 5 Department of Zoology University of São Paulo State Ocean Sciences Centre Memorial University of Newfoundland Whitney Laboratory for Marine Bioscience University of Florida

SUMMARY We examined the effect of turbidity (0.5–14 beam attenuation m–1) and predator attack speed (150 and 296 cm s–1) on escape responses of juvenile cod Gadus morhua in the laboratory. We triggered escape responses using a predator model and measured escape timing, direction and locomotor performance. We also measured responsiveness and estimated the likelihood of fish escaping the`predator attack' (putative escape success, PES). Turbidity affected both PES and the type of escape response used by the fish, but these effects depended on predator speed. PES for the fast predator attack declined from 73% in clear water to 21% in highly turbid water, due to decreased responsiveness and poorly timed escapes. Intermediate turbidity enhanced PES and responsiveness to the slow predator attack. Locomotor performance was reduced by turbidity, whereas predator speed had the opposite effect. Our results suggest that both predator attack speed and turbidity have important roles in determining the vulnerability of fish attacked by piscivorous predators.

To assess the effect of oxygen reduction on the escape response of sea bass, Dicentrarchus labrax, an integrative experimental approach was employed. The effect of hypoxia was tested on locomotor variables, i.e. cumulative distance (D), maximum swimming speed (V max) and maximum acceleration (A max). Behavioural variables, such as responsiveness (i.e. the proportion of individuals responding out of the total number of fish tested), response latency (i.e. the time interval between stimulus onset and the first detectable movement leading to the escape of the animal) and directionality (i.e. the proportion of escape responses in which the first detectable movement of the head was oriented away or towards the stimulus at its onset) were also considered. Four levels of oxygen were used: >85% (i.e. normoxia, the control treatment), 50, 20 and 10% of air saturation. Sea bass responsiveness decreased significantly at 10% of air saturation, while hypoxia did not have any effect on the response latency. At the onset of the escape response, the proportion of away/towards responses was random when oxygen was ≤50% of air saturation, suggesting an impairment of the left–right discrimination. Whatever the level of hypoxia, none of the locomotor variables (i.e. D, V max and A max) was significantly different from normoxia. Our study suggests that hypoxia may reduce sea bass elusiveness facing a predator by directly affecting its escape behaviour, possibly related to an impairment of the mechano-sensory performance and/or in the Mauthner cells involved in triggering the escape response.

Escape performance was investigated in the golden grey mullet Liza aurata exposed to various levels of oxygen: >85 (i.e. normoxia), 50 20 and 10 % air saturation. Since the golden grey mullet performed aquatic surface respiration when air saturation approached 15-10 %, escape performance was tested at 10 % air saturation with and without access to the surface (10 % S and 10 % C, respectively). Various locomotor and behavioural variables were measured, such as cumulative distance, maximum subliming speed, acceleration, responsiveness (per cent of responding fish), response latency and directionality. Golden grey mullet showed a decrease in responsiveness when the oxygen level was reduced to 10 % air saturation, whether the surface access was obstructed or not. Hypoxia did not have any effect on the response latency. Cumulative distance and maximum swimming speed over a fixed time were significantly different between normoxic conditions and 10 % C, while no differences were found in maximum acceleration. While the fish's 'C-bend' was mainly directed away from the stimulus in normoxia, the proportion of away and towards 'C-bend' was random when the oxygen was

The locomotor performance of the Mediterranean sea urchin Paracentrotus lividus was investigated under laboratory conditions. Individuals were placed singly in the centre of a glass surface positioned either horizontally or vertically in tanks with seawater, and their locomotor activity was recorded. For locomotion on a horizontal surface, speed increased with both sea urchin diameter and their straightness of path. Speeds on a vertical surface were size-independent and not related to the straightness of path, although they were affected by vertical path orientation, with the highest speeds occurring for downward movements and the slowest speeds for the upward movements. Taken together, these results suggest that the scaling of sea urchin locomotion may follow similar laws to those of legged animals, for which locomotor performance increases with size on horizontal surface, while their relative cost of locomotion increases with body size on inclined surfaces. It is suggested that differences in horizontal vs vertical locomotion may also be related to differences in the underlying locomotor mechanisms, i.e. using adhesive appendices (tube feet) or levers (spines). In a second experiment, the sea urchin speed obtained during a negative phototactic response to a direct light stimulus was recorded. The results show that speed during light stimulation is higher than that during spontaneous locomotion in sea urchins of intermediate size (2·5–4 cm), suggesting that, in addition to the direction of locomotion as shown by previous studies, light can also have an effect on speed.

Ocean acidification and warming, driven by anthropogenic CO2emissions, are considered to be among the greatest threats facing marine organisms. While each stressor in isolation has been studied extensively, there has been less focus on their combined effects, which could impact key ecological processes. We tested the independent and combined effects of short-term exposure to elevated CO2and temperature on the predator–prey interactions of a common pair of coral reef fishes (Pomacentrus wardiand its predator,Pseudochromis fuscus). We found that predator success increased following independent exposure to high temperature and elevated CO2. Overall, high temperature had an overwhelming effect on the escape behaviour of the prey compared with the combined exposure to elevated CO2and high temperature or the independent effect of elevated CO2. Exposure to high temperatures led to an increase in attack and predation rates. By contrast, we observed little influence of elevated CO2on the behaviour of the predator, suggesting that the attack behaviour ofP. fuscuswas robust to this environmental change. This is the first study to address how the kinematics and swimming performance at the basis of predator–prey interactions may change in response to concurrent exposure to elevated CO2and high temperatures and represents an important step to forecasting the responses of interacting species to climate change.

[Figure][1] Paolo Domenici discusses Paul Webb's paper entitled ‘The effect of size on the fast-start performance of rainbow trout Salmo gairdneri, and a consideration of piscivorous predator–prey interactions’. A copy of the paper can be obtained from

Animals must simultaneously engage multiple functional systems in order to navigate, feed and survive in complex environments. Nearly all vertebrates perform rapid gaze-shifting eye movements called saccades, but we know little about the behaviour of saccades during rhythmic locomotion. This study examined how saccades are coordinated with locomotor movements in a pectoral-fin-propelled teleost fish, Cymatogaster aggregata , the shiner surfperch. Individual fish were filmed swimming in a flow tank at 10 cm s −1 , and timing data were analysed using circular statistics. The results reveal that C. aggregata generates saccades non-uniformly throughout the pectoral fin cycle. Saccades primarily occur during fin abduction, when a large amount of thrust is produced, and rarely occur during the thrust-free refractory phase. Because vision is known to be impaired during saccades, we hypothesize that C. aggregata synchronizes saccades with periods of high acceleration in order to stabilize retinal images during low-acceleration phases, which are nearly saccade-free.

Elasmobranchs represent important components of marine ecosystems, but they can be vulnerable to overexploitation. This has driven investigations into the population genetic structure of large-bodied pelagic sharks, but relatively little is known of population structure in smaller demersal taxa, which are perhaps more representative of the biodiversity of the group. This study explores spatial population genetic structure of the small-spotted catshark (Scyliorhinus canicula), across European seas. The results show significant genetic differences among most of the Mediterranean sample collections, but no significant structure among Atlantic shelf areas. The data suggest the Mediterranean populations are likely to have persisted in a stable and structured environment during Pleistocene sea-level changes. Conversely, the Northeast Atlantic populations would have experienced major changes in habitat availability during glacial cycles, driving patterns of population reduction and expansion. The data also provide evidence of male-biased dispersal and female philopatry over large spatial scales, implying complex sex-determined differences in the behaviour of elasmobranchs. On the basis of this evidence, we suggest that patterns of connectivity are determined by trends of past habitat stability that provides opportunity for local adaptation in species exhibiting philopatric behaviour, implying that resilience of populations to fisheries and other stressors may differ across the range of species.

The istiophorid family of billfishes is characterized by an extended rostrum or ‘bill’. While various functions (e.g. foraging and hydrodynamic benefits) have been proposed for this structure, until now no study has directly investigated the mechanisms by which billfishes use their rostrum to feed on prey. Here, we present the first unequivocal evidence of how the bill is used by Atlantic sailfish (Istiophorus albicans) to attack schooling sardines in the open ocean. Using high-speed video-analysis, we show that (i) sailfish manage to insert their bill into sardine schools without eliciting an evasive response and (ii) subsequently use their bill to either tap on individual prey targets or to slash through the school with powerful lateral motions characterized by one of the highest accelerations ever recorded in an aquatic vertebrate. Our results demonstrate that the combination of stealth and rapid motion make the sailfish bill an extremely effective feeding adaptation for capturing schooling prey.

In intertidal environments, the recurring hypoxic condition at low tide is one of the main factors affecting fish behaviour, causing broad effects on ecological interactions. We assessed the effects of hypoxia on lateralization (e.g. the tendency to turn left or right), a behaviour related to brain functional asymmetry, which is thought to play a key role in several life history aspects of fish. Using staghorn sculpin (Leptocottus armatus), a benthic fish that typically inhabits the intertidal zone, we found that hypoxia affects behavioural lateralization at population-level. On average, staghorn sculpins showed a distinct preference for right turns under normoxic conditions (> 90 % oxygen saturation), but an equal probability of turning right or left after exposure to hypoxia for 2 hours (20 % oxygen saturation). The specific turning preference observed in the staghorn sculpin control population is likely to have an adaptive value, for example in predator-prey interactions by enhancing attack success or survival from predatory attacks. Therefore the alteration of lateralization expressed by staghorn sculpins under hypoxic conditions may have far-reaching implications for species ecology and trophic interactions. Moreover, our work raises the need to study this effect in other species, in which a hypoxia-driven disruption of lateralization could affect a wider range of behaviours, such as social interactions and schooling.

Schools of herring exposed to progressive hypoxia show a peak in velocity during severe hypoxia, at 15-34% oxygen saturation, followed by a decrease in swimming speed until school disruption occurred. The observed increase in swimming speed during severe hypoxia reveals a graded response, since the lower the fish's swimming speed prior to severe hypoxia (U 95-50 , the speed at oxygen saturations between 95 and 50%), the greater the relative increase in swimming speed. The oxygen saturations at which both peak velocity and school disruption occurred were lower for fish with lowest U 95-50 , suggesting that the fish with the slowest speed U 95 50 reach their critical P O2 (at which there is respiratory distress) last, i.e. at lower oxygen saturation. At a functional level it is suggested that herring encountering hypoxia increase their speed in order to find more favourable conditions, and the magnitude of this increase is modulated by their respiratory distress. It is also hypothesised that the observed increase in speed may be related to an increase in the rate of position shifting within the school. Since the oxygen saturation at which the response to hypoxia occurs and the magnitude of the response are related to the fish's preferred speed prior to severe hypoxia, it is suggested that such a preferred speed should be measured in experiments testing the effect of hypoxia on fish behaviour.

Herring (Clupea harengus) schools encircled by killer whales Orcinus orca and swimming under threat, show higher compaction than previous data on undisturbed herring but do not show maximum compaction as it would be predicted on theoretical grounds.

Killer whales (Orcinus orca) feeding on herring (Clupea harengus) in a fjord in northern Norway were observed using underwater video. The whales cooperatively herded herring into tight schools close to the surface. During herding and feeding, killer whales swam around and under a school of herring, periodically lunging at it and stunning the herring by slapping them with the underside of their flukes while completely submerged. The kinematics of tail-slapping were analysed in detail. Tail-slaps were made up of a biphasic behaviour consisting of two phases with opposite angles of attack, a preparatory phase (negative angles of attack) and a slap phase (positive angles of attack). During the slap phase, the mean maximum angle of attack of the flukes was 47 degrees. The maximum speed of the flukes, measured at the notch, increased with whale length (L(w)) and was 2.2 L(w)s(−)(1), while the maximum acceleration of the flukes was size-independent and was 48 m s(−)(2). When killer whales slapped the herring successfully, disoriented herring appeared on the video at approximately the time of maximum fluke velocity, in synchrony with a loud noise. This noise was not heard when the tail-slaps ‘missed’ the target, suggesting that the herring were stunned by physical contact. Killer whales then ate the stunned herring one by one. Of the tail-slaps observed, 61 % were preceded by lunges into the school. We suggest that lunging was aimed at directing the school rather than at capturing the herring, since it occurred at a relatively low speed and there were no observations of the killer whales attempting to capture the herring during lunging behaviour. Given the high performance of the tail-slaps in terms of speed and acceleration, we suggest that tail-slapping by killer whales is a more efficient strategy of prey capture than whole-body attacks, since acceleration and manoeuvrability are likely to be poor in such large vertebrates.

The escape behaviour of solitary herring (Clupea harengus L.) startled by a sound stimulus was observed by means of high-speed video-filming. The results were compared with data from a previous study on the escape behaviour of schooling herring. Escape responses were divided into “away responses” and “towards responses” according to the orientation of the C-bend of the body relative to the stimulus. The proportion of away responses was smaller for solitary than for schooling herring. In solitary herring, the subsequent escape trajectories of fish making initial away responses showed a bimodal pattern of distribution, with modes at 130 and 180° from the stimulus. Trajectories following towards responses, however, were mainly within the semicircle directed at the stimulus, and their pattern of distribution differed from that of away responses. This result contrasts with observations on schooling herring, whose trajectories following both initial away and towards responses are directed away from the stimulus. In addition, we measured the response latency, defined as the interval of time between stimulus presentation and the first detectable movement of the fish. Solitary herring showed a higher proportion of short-latency responses (latency

International audience; Teleost fishes exhibit wide and temporally stable inter-individual variation in a suite of aerobic and anaerobic locomotor traits. One mechanism that could allow such variation to persist within populations is the presence of tradeoffs between aerobic and anaerobic performance, such that individuals with a high capacity for one type of performance have a reduced capacity for the other. We investigated this possibility in European seabass Dicentrarchuslabrax, each measured for a battery of indicators of maximum locomotor performance. Aerobic traits comprised active metabolic rate, aerobic scope for activity, maximum aerobic swimming speed, and stride length, using a constant acceleration test. Anaerobic traits comprised maximum speed during an escape response, maximum sprint speed, and maximum anaerobic burst speed during constant acceleration. The data provided evidence of significant variation in performance among individuals, but there was no evidence of any trade-offs among any traits of aerobic versus anaerobic swimming performance. Furthermore, the anaerobic traits were not correlated significantly among each other, despite relying on the same muscular structures. Thus, the variation observed may reflect trade-offs with other morphological, physiological or behavioural traits.

Summary 1. Biological responses to warming are presently based on the assumption that species will remain within their bioclimatic envelope as environmental conditions change. As a result, changes in the relative abundance of several marine species have been documented over the last decades. This suggests that warming may drive novel interspecific interactions to occur (i.e. invasive vs. native species) or may intensify the strength of pre-existing ones (i.e. warm vs. cold adapted). For mobile species, habitat relocation is a viable solution to track tolerable conditions and reduce competitive costs, resulting in ‘winner’ species dominating the best quality habitat at the expense of ‘loser’ species. 2. Here, we focus on the importance of warming in exacerbating interspecific interactions between two sympatric fishes. We assessed the relocation response of the cool-water fish Coris julis (a potential ‘loser’ species in warming scenarios) at increasing relative dominance of the warm-water fish Thalassoma pavo (a ‘winner’ species). These wrasses are widespread in the Mediterranean nearshore waters. C. julis tolerates cooler waters and is found throughout the basin. T. pavo is common along southern coasts, although the species range is expanding northwards as the Mediterranean warms. 3. We surveyed habitat patterns along a thermo-latitudinal gradient in the Western Mediterranean Sea and manipulated seawater temperature under two scenarios (present day vs. projected) in outdoor arenas. Our results show that the cool-water species relocates to a lesspreferred seagrass habitat and undergoes lower behavioural performance in warmer environments, provided the relative dominance of its warm-water antagonist is high. 4. The results suggest that expected warming will act synergistically with increased relative dominance of a warm-water species to cause a cool-water fish to relocate in a less-preferred habitat within the same thermal environment. 5. Our study highlights the complexity of climate change effects and has broad implications for predictive models of responses to warming. To achieve more accurate predictions, further consideration is needed of the pervasive importance of species interactions. We believe these fundamental issues to be addressed to understand the biotic consequences of climate change.

Ventilation frequency (F(V) ) in motionless common sole Solea solea was measured before and after a startling stimulus in normoxia and in hypoxia (15% air saturation). Startling reduced F(V) in normoxia (from mean ±s.e. 41 ± 3·3 beats min⁻¹ to near zero, i.e. 2·0 ± 1·8 beats min⁻¹) and in hypoxia (from mean ±s.e. 80 ± 4·4 to 58·8 ± 12·9 beats min⁻¹). It is suggested that the maintenance of high F(V) in hypoxia may increase the probability of detection by predators compared to normoxia.

The escape behaviour of schooling herring startled by an artificial sound stimulus was observed by means of high speed video filming. Response latencies showed two distinct peaks, at 30 ms and c. 100 ms. Escape responses belonging to the two latency groups showed different turning rates during the first stage of the response, and showed different escape trajectories. We suggest that long latency escapes may be responses to startled neighbours or simply weak responses to the sound stimulus. In addition, the different contraction rates during the C-bend formation seen in the two latency groups may imply differences in the neuronal commands. The escape responses of herring were directed away from the stimulus more often than towards it (88% of the total). These away responses were more common in long latency responses, suggesting that the latter enable herring to be more accurate in discerning the direction of the threat. Startled fish contracting their body towards the stimulus (performing a towards response) appear to correct their escape course, since their escape trajectory distribution is non-uniformty distributed around 360° and directed away from the stimulus. We hypothesize that when herring are schooling, the ability of each fish to correct its trajectory following turns towards the stimulus is enhanced.

Elevated carbon dioxide (CO 2 ) has recently been shown to affect chemosensory and auditory behaviour, and activity levels of larval reef fishes, increasing their risk of predation. However, the mechanisms underlying these changes are unknown. Behavioural lateralization is an expression of brain functional asymmetries, and thus provides a unique test of the hypothesis that elevated CO 2 affects brain function in larval fishes. We tested the effect of near-future CO 2 concentrations (880 µatm) on behavioural lateralization in the reef fish, Neopomacentrus azysron . Individuals exposed to current-day or elevated CO 2 were observed in a detour test where they made repeated decisions about turning left or right. No preference for right or left turns was observed at the population level. However, individual control fish turned either left or right with greater frequency than expected by chance. Exposure to elevated-CO 2 disrupted individual lateralization, with values that were not different from a random expectation. These results provide compelling evidence that elevated CO 2 directly affects brain function in larval fishes. Given that lateralization enhances performance in a number of cognitive tasks and anti-predator behaviours, it is possible that a loss of lateralization could increase the vulnerability of larval fishes to predation in a future high-CO 2 ocean.

The behavioural responses of wild (predator-experienced) and hatchery-reared (predator-naive) cod Gadus morhua to standardized mechano-acoustic (MA) stimuli were compared in the laboratory. Wild fish responded mainly with freezing and fast-start escapes away from the stimulus, whereas hatchery-reared fish often ignored or approached the stimulus. Wild fish also had stronger responses, turning faster during escapes and reducing activity immediately after the stimulus. Both fish types were less active on a 'risky' bare substratum after the stimulus. The antipredator responses of wild fish were consistent to repeated stimuli, whereas hatchery-reared fish that had generally only encountered harmless stimuli showed more variable responses with lower repeatability. This suggests that experience plays a role in shaping the behavioural response of fishes to MA stimuli.