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This study investigated the movement patterns of yellow moray eels Gymnothorax prasinus using acoustic telemetry. Gymnothorax prasinus were found to use multiple sites within a localized area or home range.

The mechanosensory lateral line is found in all aquatic fish and amphibians. It provides a highly sensitive and versatile hydrodynamic sense that is used in a wide range of behavior. Hydrodynamic stimuli of biological interest originate from both abiotic and biotic sources, and include water currents, turbulence and the water disturbances caused by other animals, such as prey, predators and conspecifics. However, the detection of biologically important stimuli often has to occur against a background of noise generated by water movement, or movement of the fish itself. As such, separating signal and noise is "of the essence" in understanding the behavior and physiology of mechanoreception. Here we discuss general issues of signal and noise in the lateral-line system and the behavioral and physiological strategies that are used by fish to enhance signal detection in a noisy environment. In order for signal and noise to be separated, they need to differ, and we will consider those differences under the headings of: frequency and temporal pattern; intensity discrimination; spatial separation; and mechanisms for the reduction of self-generated noise. We systematically cover the issues of signal and noise in lateral-line systems, but emphasize recent work on self-generated noise, and signal and noise issues related to prey search strategies and collision avoidance.

Understanding lateral line function requires a background of lateral line anatomy combined with carefully crafted behavioral and neurophysiological studies. This combination, called neuroethology, provides the best insight into how an unfamiliar sensory system generates biologically useful information, and how this information guides behavior.

Aggregations of organisms, ranging from zooplankton to whales, are an extremely common phenomenon in the pelagic zone; perhaps the best known are fish schools. Social aggregation is a special category that refers to groups that self-organize and maintain cohesion to exploit benefits such as protection from predators, and location and capture of resources more effectively and with greater energy efficiency than could a solitary individual. In this review we explore general aggregation principles, with specific reference to pelagic organisms; describe a range of new technologies either designed for studying aggregations or that could potentially be exploited for this purpose; report on the insights gained from theoretical modelling; discuss the relationship between social aggregation and ocean management; and speculate on the impact of climate change. Examples of aggregation occur in all animal phyla. Among pelagic organisms, it is possible that repeated co-occurrence of stable pairs of individuals, which has been established for some schooling fish, is the likely precursor leading to networks of social interaction and more complex social behaviour. Social network analysis has added new insights into social behaviour and allows us to dissect aggregations and to examine how the constituent individuals interact with each other. This type of analysis is well advanced in pinnipeds and cetaceans, and work on fish is progressing. Detailed three-dimensional analysis of schools has proved to be difficult, especially at sea, but there has been some progress recently. The technological aids for studying social aggregation include video and acoustics, and have benefited from advances in digitization, miniaturization, motion analysis and computing power. New techniques permit three-dimensional tracking of thousands of individual animals within a single group which has allowed novel insights to within-group interactions. Approaches using theoretical modelling of aggregations have a long history but only recently have hypotheses been tested empirically. The lack of synchrony between models and empirical data, and lack of a common framework to schooling models have hitherto hampered progress; however, recent developments in this field offer considerable promise. Further, we speculate that climate change, already having effects on ecosystems, could have dramatic effects on aggregations through its influence on species composition by altering distribution ranges, migration patterns, vertical migration, and oceanic acidity. Because most major commercial fishing targets schooling species, these changes could have important consequences for the dependent businesses.

Behaviour and distribution of striped marlin within the southwest Pacific Ocean were investigated using electronic tagging data collected from 2005-2008. A continuous-time correlated random-walk Kalman filter was used to integrate double-tagging data exhibiting variable error structures into movement trajectories composed of regular time-steps. This state-space trajectory integration approach improved longitude and latitude error distributions by 38.5 km and 22.2 km respectively. Using these trajectories as inputs, a behavioural classification model was developed to infer when, and where, 'transiting' and 'area-restricted' (ARB) pseudo-behavioural states occurred. ARB tended to occur at shallower depths (108 ± 49 m) than did transiting behaviours (127 ± 57 m). A 16 day post-release period of diminished ARB activity suggests that patterns of behaviour were affected by the capture and/or tagging events, implying that tagged animals may exhibit atypical behaviour upon release. The striped marlin in this study dove deeper and spent greater time at ≥ 200 m depth than those in the central and eastern Pacific Ocean. As marlin reached tropical latitudes (20-21 °S) they consistently reversed directions, increased swimming speed and shifted to transiting behaviour. Reversals in the tropics also coincided with increases in swimming depth, including increased time ≥ 250 m. Our research provides enhanced understanding of the behavioural ecology of striped marlin. This has implications for the effectiveness of spatially explicit population models and we demonstrate the need to consider geographic variation when standardizing CPUE by depth, and provide data to inform natural and recreational fishing mortality parameters.

Elasmobranch fish have an electrosensory system which they use for prey detection and for orientation. Sensory inputs to this system are corrupted by a form of reafference generated by the animal’s own ventilation, but this noise is reduced by sensory processing within the medullary nucleus of the electrosensory system. This noise cancellation is achieved, at least in part, by a common mode rejection mechanism. In this study we have examined characteristics of neurones within the medullary nucleus in an attempt to understand the neural circuitry responsible for common mode suppression. Our results are in accord with previous indications that ascending efferent neurones of the medullary nucleus are monosynaptically activated from the ipsilateral electrosensory nerves and project to the midbrain. We demonstrate that in Raja erinacea, as has been previously shown in one other species (Cephaloscyllium isabella), ascending efferent neurones typically have a discrete focal excitatory receptive field and an inhibitory receptive field which may be discrete or diffuse and which often includes a contralateral component. We identify a group of interneurones within the medullary nucleus which are driven monosynaptically from the electrosensory nerves, have simple discrete excitatory receptive fields and respond vigorously to imposed common mode signals. The simplest model of the circuitry underlying common mode rejection that is consistent with the evidence is that direct afferent input impinges onto the basal dendrites of the ascending efferent neurones and onto interneurones within the nucleus, and the interneurones in turn inhibit the ascending efferents. The pattern of this projection, including commissural inputs, determines the nature and extent of ascending efferents’ inhibitory surrounds and mediates the suppression of common mode signals.

Torrent fish feeding on natural prey in an artificial stream were studied under conditions of total darkness. The distance at which prey could be detected increased with size of prey, and decreased...

Four species of nototheniid fish were sampled from below the sea ice near Cape Armitage, McMurdo Sound:Pagothenia borchgrevinki from just below the ice 1.5 km offshore,Trematomus bernacchii, Trematomus hansoni andTrematomus centronotus from off the bottom in about 20 m of water near the shore. Scale worms and isopods were conspicuous non-planktonic prey, and present in the three benthic fish species. The planktonic pteropod molluscLimacina helicina was numerically common in all four species of fish. The planktonic hyperiid amphipodHyperiella dilatata was also found in all fish species. WhereasP. borchgrevinki is planktivorous in accord with its pelagic habit, theTrematomus spp. clearly also feed on plankton from the water column.T. hansoni is particularly planktivorous, taking smaller copepods thanP. borchgrevinki.

SUMMARY Blind Mexican cave fish (Astyanax fasciatus) sense the presence of nearby objects by sensing changes in the water flow around their body. The information available to the fish using this hydrodynamic imaging ability depends on the properties of the flow field it generates while gliding and how this flow field is altered by the presence of objects. Here, we used particle image velocimetry to measure the flow fields around gliding blind cave fish as they moved through open water and when heading towards a wall. These measurements, combined with computational fluid dynamics models, were used to estimate the stimulus to the lateral line system of the fish. Our results showed that there was a high-pressure region around the nose of the fish, low-pressure regions corresponding to accelerated flow around the widest part of the body and a thick laminar boundary layer down the body. When approaching a wall head-on, the changes in the stimulus to the lateral line were confined to approximately the first 20% of the body. Assuming that the fish are sensitive to a certain relative change in lateral line stimuli, it was found that swimming at higher Reynolds numbers slightly decreased the distance at which the fish could detect a wall when approaching head-on, which is the opposite to what has previously been expected. However, when the effects of environmental noise are considered, swimming at higher speed may improve the signal to noise ratio of the stimulus to the lateral line.

The mechanosensory lateral line is found in all fish and some amphibia and responds to hydrodynamic stimuli such as water movement and vibration. Biological behavior is all about mating, feeding, and moving about safely in between times, and hydrodynamic information encoded by the lateral line can play a critical role in all these behaviors. Examples include mating communication; detection of prey through the water vibrations, surface waves, or hydrodynamic trails; and orientation to water currents. Even though the lateral line is restricted to fish and amphibia, analogous vibration senses conferring similar behavioral capability also occur in reptiles, birds, and mammals.

Elasmobranch fishes have an electroreceptive system which they use for prey detection and orientation. Sensory inputs in this system are corrupted by a form of reafference generated by the animal’s own ventilation. However, we show here that in the carpet shark, Cephaloscylium Isabella, as in two previously studied batoid species, this ventilatory ‘noise’ is reduced by sensory processing within the medullary nucleus of the electrosensory system. It has been proposed that the noise cancellation is achieved by a common mode rejection mechanism. One prediction of this hypothesis is that secondary neurons within the medullary nucleus should have both excitatory and inhibitory components to their receptive fields. This prediction is experimentally verified here. Projection neurons of the medullary nucleus in the carpet shark typically have a focal excitatory, and a diffuse inhibitory, receptive field organization including a component of contralateral inhibition. This result provides strong support for the hypothesis that ventilatory suppression in the elasmobranch electrosensory system is achieved by a common mode mechanism.

The electroreceptors of elasmobranchs are strongly modulated by the fish's own ventilation but this source of potential interference is suppressed within the medulla. The mechanism for the suppression is thought to be based on the common mode nature of the ventilatory noise, i.e. it is of the same amplitude and phase for all of the electroreceptors, compared with environmental electric fields which affect the receptors differentially. Evidence for the common mode suppression hypothesis is provided here in skates by the observation that the response to an artificial common mode stimulus that is independent of ventilation and delivered through an electrode inserted into the animal's gut is also suppressed by the medullary neurons; the extent to which a particular neuron suppresses the responses to the gut stimulus and to ventilation is similar. In addition, a potential modulation of 5–150μV is measured between the skate's interior and the sea water during ventilation and this appears to be responsible for the self-stimulation. By passing d.c. or sinusoidal currents through the gut electrode it is demonstrated that this ventilatory potential is due to the variable shunting of a standing d.c. potential across the fish's skin by the opening and closing of the mouth and gill slits during ventilation. Osmoregulatory ion-pumping appears to contribute to the production of the d.c. potential. Note: Present address: Department of Biology, Wesleyan University, Middletown, CT 06457, USA. Present address: Department of Zoology, University of Auckland, Auckland, New Zealand.

Patterns in the distribution and abundance of ichthyoplankton off the northeastern coast of New Zealand were investigated. Neuston samples were collected monthly between November 1986–November 1987 at stations located 0·5, 3·2 and 6·0 km offshore from each of three locations that were separated by 3–5 km. Three abundant taxa, tripterygiids ( Forsterygion spp.), an engraulid ( Engraulis australis ) and a clupeoid ( Sardinops neopilchardus ) accounted for 80% of the total catch. Ichthyoplankton was at least three times more abundant during the winter month of July than in any other month, primarily due to the large numbers of tripterygiids. Low densities of fish larvae were found during the spring and summer, but many taxa had peaks in abundance at this time. Patterns of along-shore distribution were inconsistent; they varied between months for most taxa. In general, more fish larvae were caught at the sampling stations that were 3·2 or 6·0 km from the shore.

Regional differences in the architecture and size of lateral line canals and neuromasts were measured in an Antarctic fish, Trematomus bernacchii, and the data were used in models of canal and cupular mechanics to predict the frequency response of these two peripheral structures. These modeled predictions were then compared to frequency response functions measured with single unit recording techniques from anterior and posterior lateral line fibers innervating different canals on the head and trunk of fish of various sizes. Despite large variations in the peripheral morphology of head and trunk canals in fish of different sizes, lateral line fibers were relatively homogeneous in their frequency response properties. In response to stimuli of equal pk-pk acceleration levels, all canal neuromast fibers responded with equal and maximum responsiveness in the 10-45 Hz range, after which responsiveness fell off at about 18 dB/octave. Whereas the biomechanical models of cupular and canal responsiveness predicted the region of equal and maximum responsiveness in the 10-45 Hz range, they did not predict the high frequency cutoff nor the slope. Rather, these models predicted responsiveness out to at least 540 Hz, and a high frequency slope of 12 dB/octave. In terms of the frequency response of peripheral fibers, we conclude that (1) there can be considerable morphological variability, with little consequence for function, as long as some minimum standards for maintaining constant acceleration responsiveness in the 10-45 Hz range are met, and (2) there must be additional filters between the cupula and primary afferent fibers.

The Antarctic notothenioids are a monophyletic radiation of fishes that have evolved under conditions of low light and cold, where non-visual sensory systems, such as the mechanosensory lateral line system, would be of importance. As part of a study of the structure and function of the mechanosensory lateral line system in these fishes we systematically characterized the function of the anterior lateral line system in one of the common benthic species, Trematomus bernacchii. Frequency-response and threshold-tuning curve methods yield similar functional characterizations of single afferent fibre responses to vibrational stimulation. Curve fitting of generalized transfer function to frequency-response curves allows an objective splitting of responses into velocity and acceleration sensitive populations thought to correspond to superficial and canal neuromasts, respectively. Both response types are characterized by a low-pass frequency-response curve, with a relatively low upper frequency cut-off when compared with data from temperate species. The sensitivity of the lateral line system of T. bernacchii is comparable to that of the mottled sculpin Cottus bairdi.

Water currents are extremely important in the aquatic environment and play a very significant role in the lives of fishes. Sensory processing of water currents involves a number of sensory modalities including the inner ear, vision, tactile sense and the mechanosensory lateral line. The inner ear will detect whole–body accelerations generated by changes in flow, or by turbulence, whereas visual and tactile inputs will signal translational movement with respect to an external visual or tactile reference frame. The superficial neuromasts of the mechanosensory lateral line detect flow over the surface of the body and have the appropriate anatomical distribution and physiological properties to signal the strength and the direction of flow and, hence, contribute to the detection of regional differences in flow over different parts of the body.

SUMMARYBlind Mexican cave fish (Astyanax fasciatus) lack a functioning visual system, and are known to use self-generated water motion to sense their surroundings; an ability termed hydrodynamic imaging. Nearby objects distort the flow field created by the motion of the fish. These flow distortions are sensed by the mechanosensory lateral line. Here we used image processing to measure detailed kinematics, along with a new behavioural technique, to investigate the effectiveness of hydrodynamic imaging. In a head-on approach to a wall, fish reacted to avoid collision with the wall at an average distance of only 4.0±0.2 mm. Contrary to previous expectation, there was no significant correlation between the swimming velocity of the fish and the distance at which they reacted to the wall. Hydrodynamic imaging appeared to be most effective when the fish were gliding with their bodies held straight, with the proportion of approaches to the wall that resulted in collision increasing from 11% to 73% if the fish were beating their tails rather than gliding as they neared the wall. The swimming kinematics of the fish were significantly different when swimming beside a wall compared with when swimming away from any walls. Blind cave fish frequently touched walls when swimming alongside them, indicating that they use both tactile and hydrodynamic information in this situation. We conclude that although hydrodynamic imaging can provide effective collision avoidance, it is a short-range sense that may often be used synergistically with direct touch.

The complexities of the physics of underwater acoustics, the functional similarities of the hair cells in the lateral line and ear, and the presence of mechanical linkages between the ear, lateral line and swimbladder blur any hard and fast distinctions between acoustic and hydrodynamic receptors and between acoustic and hydrodynamic stimuli (see Braun and Grande, Chapter 4). Thus, any treatment of underwater sound must address the contributions of the lateral line system in the interpretation of acoustic stimuli of biological importance. In a free-field situation (at some distance from the stimulus source, and away from physical boundaries), the acoustic field generated by a vibrating source (e.g., a monopole or dipole) is well defined mathematically (see Section 3). However, even in such a simple physical system, local flow fields close to the vibrating source (e.g., in the “nearfield”) can provide information about the source that is distinct from that provided by the propagated acoustic field (e.g., in the “farfield”). In other words, the stimulus field generated by a vibrating object includes both acoustic and hydrodynamic components and movements of the acoustic source, or the water in which a fish sits, makes the distinction between these two components of the stimulus more difficult to identify. The fact that the most interesting biology happens close to a source (within a few body lengths), and in the presence of boundaries (e.g., in a rock-lined stream, or near the ocean bottom) where simple free-field conditions do not exist, make the analysis of acoustic stimuli challenging. The structural diversity of the lateral line system, including that of both the neuromasts (canal and superficial) and lateral line canals, poses challenges to the study of lateral line function in both laboratory and natural behavioral settings and should be acknowledged in any experimental analysis.

Sharks, skates, and rays exploit a marine environment rich in bioelectric and motional electric fields, which are very weak but nevertheless very useful for prey capture, predator avoidance, social interactions, and orientation in the sea. The elasmobranchs’ appreciation of these fields is made possible by two distinct specializations. The first of these is an array of extraordinarily sensitive receptors, the ampullae of Lorenzini, which derive much of their sensitivity from positive feedback mechanisms held delicately balanced at threshold. The second specialization is a sophisticated set of filter mechanisms in the brain for extracting the weak electrosensory signals from much stronger background noise. A large portion of this background noise is created by the fish’s own movements. Recent experiments show that a remarkable adaptive filter mechanism implemented by the cerebellar-like circuitry of the medullary electrosensory nucleus accounts for much of the noise suppression. The specializations of receptors and CNS so well developed in these fishes allow us to recognize important general principles operating in other sensory systems and in other vertebrates.

The sensory abilities of fish provide the essential basis for behavioural interaction with the environment. Simple elements of behaviour can result from endogenous brain activity but even in these cases, the behaviour is shaped by sensory context or feedback. At the other end of the spectrum, sensory reflexes are behavioural elements dominated by the sensory input itself. However, most on-going behaviour is a complex interplay of central activity and sensory input. The senses provide information on the opportunities and threats presented by the environment and this information feeds into central nervous system (CNS) activity in a way that typically generates what we observe as coordinated, context appropriate behaviour.

Chondrichthyans occupy a basal place in vertebrate evolution and offer a relatively unexplored opportunity to study the evolution of vertebrate brains. This study examines the brain morphology of 22 species of deep-sea sharks and holocephalans, in relation to both phylogeny and ecology. Both relative brain size (expressed as residuals) and the relative development of the five major brain areas (telencephalon, diencephalon, mesencephalon, cerebellum, and medulla) were assessed. The cerebellar-like structures, which receive projections from the electroreceptive and lateral line organs, were also examined as a discrete part of the medulla. Although the species examined spanned three major chondrichthyan groupings (Squalomorphii, Galeomorphii, Holocephali), brain size and the relative development of the major brain areas did not track phylogenetic groupings. Rather, a hierarchical cluster analysis performed on the deep-sea sharks and holocephalans shows that these species all share the common characteristics of a relatively reduced telencephalon and smooth cerebellar corpus, as well as extreme relative enlargement of the medulla, specifically the cerebellar-like lobes. Although this study was not a functional analysis, it provides evidence that brain variation in deep-sea chondichthyans shows adaptive patterns in addition to underlying phylogenetic patterns, and that particular brain patterns might be interpreted as ‘cerebrotypes’.

The stated purpose of this book is to examine the relationships between migration, life cycles, and population/species productivity, stability and resilience. Appropriately, the chosen definition o...

A systematic study of the ambient noise in the shallow coastal waters of north-eastern New Zealand shows large temporal variability in acoustic power levels between seasons, moon phase and the time of day. Ambient noise levels were highest during the new moon and the lowest during the full moon. Ambient noise levels were also significantly higher during summer and lower during winter. Bandpass filtering (700–2,000 Hz and 2–15 kHz), combined with snap counts and data from other studies show that the majority of the sound intensity increases could be attributed to two organisms: the sea urchin and the snapping shrimp. The increased intensity of biologically produced sound during dusk, new moon and summer could enhance the biological signature of a reef and transmit it further offshore. Ambient noise generated from the coast, especially reefs, has been implicated as playing a role in guiding pelagic post-larval fish and crustaceans to settlement habitats. Determining a causal link between temporal increases in ambient noise and higher rates of settlement of reef fish and crustaceans would provide support for the importance of ambient underwater sound in guiding the settlement of these organisms.

The pelagic life history phase of reef fishes and decapod crustaceans is complex, and the evolutionary drivers and ecological consequences of this life history strategy remain largely speculative. There is no doubt, however, that this life history phase is very significant in the demographics of reef populations. Here, we initially discuss the ecology and evolution of the pelagic life histories as a context to our review of the role of acoustics in the latter part of the pelagic phase as the larvae transit back onto a reef. Evidence is reviewed showing that larvae are actively involved in this transition. They are capable swimmers and can locate reefs from hundreds of metres if not kilometres away. Evidence also shows that sound is available as an orientation cue, and that fishes and crustaceans hear sound and orient to sound in a manner that is consistent with their use of sound to guide settlement onto reefs. Comparing particle motion sound strengths in the field (8 x 10(-11) m at 5 km from a reef) with the measured behavioural and electrophysiological threshold of fishes of (3 x 10(-11) m and 10 x 10(-11), respectively) provides evidence that sound may be a useful orientation cue at a range of kilometres rather than hundreds of metres. These threshold levels are for adult fishes and we conclude that better data are needed for larval fishes and crustaceans at the time of settlement. Measurements of field strengths in the region of reefs and threshold levels are suitable for showing that sound could be used; however, field experiments are the only effective tool to demonstrate the actual use of underwater sound for orientation purposes. A diverse series of field experiments including light-trap catches enhanced by replayed reef sound, in situ observations of behaviour and sound-enhanced settlement rate on patch reefs collectively provide a compelling case that sound is used as an orientation and settlement cue for these late larval stages.

The widespread variation in brain size and complexity that is evident in sharks and holocephalans is related to both phylogeny and ecology. Relative brain size (expressed as encephalization quotients) and the relative development of the five major brain areas (the telencephalon, diencephalon, mesencephalon, cerebellum, and medulla) was assessed for over 40 species from 20 families that represent a range of different lifestyles and occupy a number of habitats. In addition, an index (1–5) quantifying structural complexity of the cerebellum was created based on length, number, and depth of folds. Although the variation in brain size, morphology, and complexity is due in part to phylogeny, as basal groups have smaller brains, less structural hypertrophy, and lower foliation indices, there is also substantial variation within and across clades that does not reflect phylogenetic relationships. Ecological correlations, with the relative development of different brain areas as well as the complexity of the cerebellar corpus, are supported by cluster analysis and are suggestive of a range of ‘cerebrotypes’. These correlations suggest that relative brain development reflects the dimensionality of the environment and/or agile prey capture in addition to phylogeny.

The pelagic life history phase of reef fishes and decapod crustaceans is complex, and the evolutionary drivers and ecological consequences of this life history strategy remain largely speculative. There is no doubt, however, that this life history phase is very significant in the demographics of reef populations. Here, we initially discuss the ecology and evolution of the pelagic life histories as a context to our review of the role of acoustics in the latter part of the pelagic phase as the larvae transit back onto a reef. Evidence is reviewed showing that larvae are actively involved in this transition. They are capable swimmers and can locate reefs from hundreds of metres if not kilometres away. Evidence also shows that sound is available as an orientation cue, and that fishes and crustaceans hear sound and orient to sound in a manner that is consistent with their use of sound to guide settlement onto reefs. Comparing particle motion sound strengths in the field (8 × 10−11 m at 5 km from a reef) with the measured behavioural and electrophysiological threshold of fishes of (3 × 10−11 m and 10 × 10−11, respectively) provides evidence that sound may be a useful orientation cue at a range of kilometres rather than hundreds of metres. These threshold levels are for adult fishes and we conclude that better data are needed for larval fishes and crustaceans at the time of settlement. Measurements of field strengths in the region of reefs and threshold levels are suitable for showing that sound could be used; however, field experiments are the only effective tool to demonstrate the actual use of underwater sound for orientation purposes. A diverse series of field experiments including light‐trap catches enhanced by replayed reef sound, in situ observations of behaviour and sound‐enhanced settlement rate on patch reefs collectively provide a compelling case that sound is used as an orientation and settlement cue for these late larval stages.

Publisher Summary Polar fishes feed, grow, and reproduce at low temperature, making them an important model for understanding temperature adaptation. Other fish may survive cold winters, but polar fish conduct their entire life cycle in frigid water. This chapter discusses the physiology or function of the nervous system and the sensory organs of polar fishes. It addresses the issue of temperature adaptation in the nervous system and discusses what is special about the neurophysiology of fish from stenothermal arctic and antarctic environments, what themes are common to both groups, and how the polar species differ from fishes that are more eurythermal yet can acclimatize to severe cold. The extent to which antarctic fish have optimized their critical cellular and neural systems to operate at subzero temperatures is reflected in their extreme stenothermy. This chapter discusses antarctic species rather than arctic species.

Water movements, of both abiotic and biotic origin, provide a wealth of information for fishes. They detect these water movements by arrays of hydrodynamic sensors located on the surface of the body as superficial neuromasts and embedded in subdermal lateral line canals. Recently, the anatomical dichotomy between superficial and canal neuromasts has been matched by demonstrations of a corresponding functional dichotomy. Superficial neuromasts are sensitive to water flows over the surface of the fish and are the sub-modality that participates in orientation to water currents, a behaviour known as rheotaxis. The canal neuromasts are sensitive to water vibration and it is this sub-modality that determines the localization of artificial prey. Recently, however, it has been shown that the complex behaviour of natural prey capture in the dark requires input from both lateral line sensory submodalities and here we show that the ability of trout to hold station behind a stationary object in fast flowing water also requires integration of information from both sub-modalities.

Chemosensory communication may be crucial during mate choice and mating in the southern temperate spiny lobster Jasus edwardsii to ensure that females mate with large males capable of supplying adequate numbers of sperm during the short mating window. To clarify the role of pheromones during this process, three laboratory experiments were carried out. In an experiment where the output of urine, which contains sex-specific pheromones, from large and small catheterized males was switched, large post-molt females did not make a clear choice of mate. This indicates that while females distinguish among females, males, and juveniles using their chemosensory sense, they distinguish among males using visual and tactile senses in combination with olfaction. Further, two antennule-ablation experiments were carried out to determine if detection of pheromones by the antennules of females or males was critical for mate selection, courting, or mating. In both cases, we observed a (nonsignificant) trend of slightly delayed mating of treatment females. We found that disruption of female olfaction causes less impact on courtship or mating than ablation of male antennules which increased the variance in the length of the period between molting and mating and resulted in a systematic reduction in clutch size. This lesser impact of female ablation may be because females can still respond to their own internal cues about egg ripeness whereas males cannot. In J. edwardsii, unlike the American clawed lobster, Homarus americanus, one fully functional partner of either sex appears sufficient to initiate mating.

Specimens of 4 species of Antarctic fish were captured at different locations in McMurdo Sound during the early summer, and for one species also during late winter. Stomach contents were analysed to examine resource utilization across species, at different locations, and between late winter and early summer. The results are consistent with earlier findings that there is a gradation in resource utilization across these species.T. pennelli andT. bernacchii tend to take predominantly benthic crawling prey, though they also take prey from the water column.T. hansoni andT. nicolai tend to take more prey from the water column, a tendency which can be related to the visual feeding vector of these species. Substantial differences in diet for the same species captured in different locations indicated significant flexibility in prey selection which would allow utilization of spatial and temporal fluctuations in prey availability. Successful feeding byT. bernacchii in late winter is a further indication that this species can feed non-visually and supports the notion that non-visual feeding mechanisms are likely to be of importance in the biology of the Antarctic fishes.

The mechanoreceptive lateral line system detects hydrodynamic stimuli and plays an important role in a number of types of fish behaviour, including orientation to water currents. The lateral line is composed of hair cell receptor organs called neuromasts that occur as superficial neuromasts on the surface of the skin or canal neuromasts located in subepidermal canals. Both are innervated by primary afferents of the lateral line nerves. Although there have been extensive studies of the response properties of lateral line afferents to vibrating sources, their response to water flow has not been reported. In this study, we recorded extracellularly from anterior lateral line afferents in the New Zealand long-fin eel Anguilla dieffenbachii while stimulating the eel with unidirectional water flows at 0.5–4 cm s−1. Of the afferents, 80 % were flow-sensitive to varying degrees, the response magnitude increasing with flow rate. Flow-sensitive fibres gave non-adapting tonic responses, indicating that these fibres detect absolute flow velocity. Further studies are needed to confirm whether flow-sensitive and flow-insensitive fibres correlate with superficial and canal neuromasts, respectively.

The radiation of notothenioid fishes provides an excellent system to explore issues of evolution and adaptation. Most studies emphasize adaptation to the extreme Antarctic environment; however, recent work provides cogent examples of disaptation or evolutionary loss of function. The nature and extent of regressive change is revealed by subsequent adaptive recovery. Ancestral notothenioids were benthic but some became secondarily pelagic through the retention of larval characters. Paedomorphosis has produced detrimental changes in lateral-line sensory systems that have been made good by compensatory adaptation. In the icefish family, compensatory adaptation has followed the loss of the oxygen-binding pigments haemoglobin and myoglobin.

Hearing in its broadest sense is the detection, by specialized mechanoreceptors, of mechanical energy propagated through the environment. In terrestrial vertebrates, this typically means inner ear transduction of air pressure waves radiating out from a sound source, though the detection of substrate vibrations can also be considered as a form of hearing. In aquatic environments, the extended contribution of incompressible flow in the near field of the source adds additional complexities, and both incompressible flow and propagated pressure waves are detected by a range of specialized hair cell mechanosensory systems. Hair cells are generalized mechanical transducers that respond to mechanical deformation of the receptor hairs at their apical surface. One of the interesting stories of hearing in general, and in aquatic vertebrates in particular, is how the structures associated with hair cell organs play a major role in modifying or channeling the environmental stimulus onto the hair cell receptors. Hence the peripheral anatomy determines to a large degree what particular stimulus feature is being encoded at the level of the hair cell.

There are many similarities between Antarctic seas and the deep ocean the principal ones being that both are cold and dark. Antarctic high latitude basins are effectively dark for the duration of the Antarctic winter. Even during summer, ice cover extensively reduces light levels, and the continental shelf is deeper (∼600 m) than for other continents (∼200 m).

The generation of expectations about sensory input and the subtraction of such expectations from actual input appear to be important features of sensory processing. This paper describes the generation of sensory expectations within cerebellum-like structures of four distinct groups of fishes: Mormyridae; Rajidae; Scorpaenidae; and Apteronotidae. These structures consist of a sheet-like array of principal cells. Apical dendrites of the principal cells extend out into a molecular layer where they are contacted by parallel fibers. The basilar regions of the arrays receive primary afferent input from octavolateral endorgans, i.e., electroreceptors, mechanical lateral line neuromasts, or eighth nerve endorgans. The parallel fibers in the molecular layer convey various types of information, including corollary discharge signals associated with motor commands, sensory information from other modalities such as proprioception, and descending input from higher stages of the sensory modality that is processed by the structure. Associations between the signals conveyed by the parallel fibers and particular patterns of sensory input to the basal layers lead to the generation of a negative image of expected sensory input within the principal cell array. Addition of this negative image to actual sensory input results in the subtraction of expected from actual input, allowing the unexpected or novel input to stand out more clearly. Intracellular recording indicates that the negative image is probably generated by means of anti-Hebbian synaptic plasticity at the parallel fiber to principal cell synapse. The results are remarkably similar in the different fishes and may generalize to cerebellum-like structures in other sensory systems and taxa.

Publisher Summary This chapter discusses the sensory physiology of deep sea fishes. The olfactory receptor cells are located in an epithelium lining the floor of the nasal capsule and this epithelium is typically folded into olfactory lamellae. The geometry and number of olfactory lamellae within the nasal capsule and the organization of the sensory and nonsensory epithelia vary widely among different fish species. It is predicted that a horizontal patch of detectable pheromone will expand to a maximum range of almost 100 m in about 9 h and then fully dissipate in about 1 day. The pattern of bioluminescent flashing has been observed in two Lampanyctus species, which suggest that the distinct flash patterns may permit species recognition among species that otherwise have similar photophore arrays and also have overlapping habitats. A visual system geared to the interception of bioluminescent signals is found in Bujuculifimzia drukei . The potential for tactile stimuli to play a role in prey detection is shown in antarctic fishes. Antarctic benthic feeders show stereotypical responses to prey touching their pelvic or anal fins.

The New Zealand bigeye,Pempheris adspersa, is a nocturnal planktivore and has recently been found to be an active sound producer. The rostral end of the swim bladder lies adjacent to Baudelot's ligament which spans between the bulla and the cleithrum bone of the pectoral girdle. The aim of this study was to use the auditory evoked potential technique to physiologically test the possibility that this structure provides an enhanced sensitivity to sound pressure in the bigeye. At 100 Hz, bigeye had hearing sensitivity similar to that of goldfish (species with a mechanical connection between the swim bladder and the inner ear mediated by the Weberian ossicles) and were much more sensitive than other teleosts without ancillary hearing structures. Severing Baudelot's ligament bilaterally resulted in a marked decrease in hearing sensitivity, as did swim bladder puncture or lateral line blockage. These results show that bigeye have an enhanced sensitivity to sound pressure and provide experimental evidence that the functional basis of this sensitivity represents a novel hearing specialization in fish involving the swim bladder, Baudelot's ligament and the lateral line.

In lateral line and electrosensory systems of fish, the animal's own movements create unwanted stimulation that could interfere with the detection of biologically important signals. Here we report that an adaptive filter in the medullary nuclei of both senses suppresses self-stimulation. Second-order electrosensory neurons in an elasmobranch fish and mechanosensory neurons in a teleost fish learn to cancel the effects of stimuli that are presented coupled to the fish's movements. A model is proposed for how the adaptive filter is realized by the cerebellar-like circuits of the hindbrain nuclei in these senses.

Ocular morphology was examined in larval, juvenile and adult F. varium. There was a 26-fold increase in eye size from 0.28 mm in the smallest larva (5.0 mm in length) to a maximum diameter of 7.2 mm in a 110 mm long adult. Larval fish had pure cone retinae at hatching, however, putative rod precursor cells were also present. Juvenile and adult fish had a duplex retina with cones arranged in a square mosaic in which 4 equal double cones surrounded a central single cone. Hypertrophy of cone ellipsoids with increasing eye size resulted in maintenance of a closely packed array in fishes of all sizes. Theoretical sensitivity, assessed in terms of convergence of rods:bipolars, rod density, and photoreceptor outer segment length, increased during the juvenile phase but was constant across the adult size range. Angular density of cones increased with increasing eye size such that theoretical spacial acuity was poor in smallest fish (1 degree 8') and improved to an asymptotic value of about 9' in adults. Behavioural acuity of a 1-day-old larva determined using the optokinetic response (29 degrees), was very much poorer than histological estimates (1 degree 8'). Behavioural acuity improved to 4 degrees 18' at 14 days of age, compared to a theoretical value of 54'. An estimate of Matthiessen's ratio based on histological measurements suggests that the larval eye is initially strongly myopic, and grows into focus. Development of the retractor lentis muscle was first apparent 7 days after hatching with the result that larval eyes are incapable of accommodative lens movements to correct for a refractive error. This apparent myopia is thought to account for at least part of the mismatch between theoretical and behavioural spatial acuity.

Any treatise on the evolution of hearing inevitably raises the possibility that the vertebrate auditory system has evolved from the mechanosensory lateral line system known to exist in the earliest vertebrates. The arguments for (van Bergeijk 1967; Jorgensen 1989) and against (Wever 1976; Northcutt 1981) this “octavolateralis” hypothesis, first proposed by Ayers (1892), have depended primarily on anatomical and developmental comparisons between the two systems. It is questionable whether this issue can or ever will be resolved, but the frequency with which it has been addressed in the past and is currently being addressed in this volume (Popper, Piatt, and Edds, Chapter 4; Fritzsch, Chapter 18) testifies to the fascination it holds for anyone interested in the evolution of ears and hearing.

Tethering prey is often used to help determine the impact of predators in aquatic communities. In this study, a novel photographic tethering device was used to make digital recordings of predation events on juveniles of the spiny lobster, Jasus edwardsii. Predation of lobsters was significantly higher during the day (76%) than at night (33.4%). This was consistent with a SCUBA survey that found greater numbers of diurnal predators than nocturnal predators at the study site. However, the abundance of predators was not consistent with the number of predation events for individual species as recorded by the photographic tethering device. The snapper, Pagrus auratus, was the most abundant species at the study site (45% of all diurnally active fishes), but was only responsible for 12% of predation events during the day. In contrast, wrasse species were responsible for the greatest number of predation events during the day (60%), yet made up only a small proportion of the diurnal fish population (25%). The results of this study indicate the importance of determining the identity of potential predators, through the use of a photographic tethering device, for increasing the value of results generated from tethering experiments.

Temperature change has a major impact on the function of the nervous system and its components, including altering synaptic gain and changing synaptic and conduction delays. Although many animals are subject to changes in body temperature, the degree of temperature change actually experienced by many poikilotherms is not well documented. The fact that many animals continue to exhibit coordinated sensorimotor function during changes in body temperature indicates that some form of temperature compensation has occurred within the nervous system. Compensations may occur automatically (opposing effects of temperature offsetting each other), they may be an inherent property of closed-loop systems, or they may be effected by more sophisticated control mechanisms such as those of the vertebrate cerebellum.