Head Morphology and Electrosensory Pore Distribution of Carcharhinid and Sphyrnid Sharks

Selection to maximize electroreceptive search area might have driven evolution of the cephalofoil head morphology of hammerhead sharks (family Sphyrnidae). The enhanced electrosensory hypothesis predicts that the wider head of sphyrnid sharks necessitates a greater number of electrosensory pores to maintain a comparable pore density. Although gross head morphology clearly differs between sphyrnid sharks and their closest relatives the carcharhinids, a quantitative examination is lacking. Head morphology and the distribution of electrosensory pores were compared between a carcharhinid, Carcharhinus plumbeus, and two sphyrnid sharks, Sphyrna lewini and S. tiburo. Both sphyrnids had greater head widths than the carcharhinid, although head surface area and volume did not differ between the three species. The raked head morphology of neonatal S. lewini pups, presumably an adaptation to facilitate parturition, becomes orthogonal to the body axis immediately post-parturition whereas this change is much less dramatic for the other two species. The general pattern of electrosensory pore distribution on the head is conserved across species despite the differences in gross head morphology. Sphyrna lewini has a mean of 3067 ± 158.9 SD pores, S. tiburo has a mean of 2028 ± 96.6 SD pores and C. plumbeus has a mean of 2317 ± 126.3 SD pores and the number of pores remains constant with age. Sphyrnids have a greater number of pores on the ventral surface of the head whereas C. plumbeus has an even distribution on dorsal and ventral surfaces. The greater number of pores distributed on a similar surface area provides S. lewini pups with a higher density of electrosensory pores per unit area compared to C. plumbeus pups. The greater number of ampullae, the higher pore density and the larger sampling area of the head combine to provide hammerhead sharks with a morphologically enhanced electroreceptive capability compared to comparably sized carcharhinids.     

The Neuroecology of the Elasmobranch Electrosensory World: Why Peripheral Morphology Shapes Behavior

The adaptations of elasmobranch sensory systems can be studied by linking the morphological structure with the natural behavior and ecology of the organism. This paper presents the first step in a neuroecological approach to interpret the spatial arrangement of the electrosensory ampullary organs in elasmobranch fishes. A brief review of the structure and function of the ampullae of Lorenzini is provided for interpretation of the organ system morphology in relation to the detection of dipole and uniform electric fields. The spatial projections of canals from discrete ampullary clusters were determined for the barndoor skate, Raja laevis, based upon a published figure in Raschi (1986), and measured directly from the head of the white shark, Carcharodon carcharias. The dorsoventrally flattened body of the skate restricts the projections of long canals to the horizontal plane. There is a distinct difference between dorsal and ventral projection patterns in all groups. Notable within-cluster features include a relatively long canal subgroup in the dorsal superficial ophthalmic (SOd) and dorsal hyoid (HYOd) clusters that are oriented parallel (bidirectionally) to the longitudinal axis of the body. It is postulated that this subgroup of canals may be important for detection and orientation to weak uniform fields. Ventral canal projections in the skate are primarily lateral, with the exception of the hyoid (HYOv) that also projects medially. This wide dispersion may function for the detection of prey located below the body and pectoral fins of the skate, and may also be used for orientation behavior. The mandibular canals located near the margin of the lower jaw (of both study species) are ideally positioned for use during prey manipulation or capture, and possibly for interspecific courtship or biting. The head of the white shark, which lacks the hyoid clusters, is ovoid in cross section and thus ampullary canals can project into three-dimensional space. The SOd and superficial ophthalmic ventral (SOv) clusters show strong rostral, dorsal and lateral projection components, whereas the SOv also detects rostral fields under the snout. In the sagittal plane, the SOv and SOd have robust dorsal projections as well as ventral in the SOv. Most notable are canal projections in the white shark buccal (BUC) ampullary cluster, which has a radial turnstile configuration on the ventrolateral side of the snout. The turnstile design and tilt between orthogonal planes indicates the white shark BUC may function in detection of uniform fields, including magnetically induced electric fields that may be used in orientation behaviors. These data can be used in future neuroecology behavioral performance experiments to (1) test for possible specializations of cluster groups to different natural electric stimuli, (2) the possibility of specialized canal subgroups within a cluster, and (3) test several models of navigation that argue for the use of geomagnetically induced electric cues.     

Response properties and biological function of the skate electrosensory system during ontogeny

This study examined the response properties of skate electrosensory primary afferent neurons of pre-hatch embryo (8–11 weeks), post-hatch juvenile (1–8 months), and adult (>2 year) clearnose skates (Raja eglanteria) to determine whether encoding of electrosensory information changes with age, and if the electro-sense is adapted to encode natural bioelectric stimuli across life history stages. During ontogeny, electrosensory primary afferents increase resting discharge rate, spike regularity, and sensitivity at best frequency. Best frequency was at 1–2 Hz for embryos, showed an upwards shift to 5 Hz in juveniles, and a downward shift to 2–3 Hz in adults. Encapsulated embryos exhibit ventilatory movements that are interrupted by a “freeze response”” when presented with weak uniform fields at 0.5 and 1 Hz. This phasic electric stimulus contains spectral information found in potentials produced by natural fish predators, and therefore indicates that the embryo electrosense can efficiently mediate predator detection and avoidance. In contrast, reproductively active adult clearnose skates discharge their electric organs at rates near the peak frequency sensitivity of the adult electrosensory system, which; facilitates electric communication during social behavior. We suggest that life-history-dependent functions such as these may shape the evolution of the low-frequency response properties for the elasmobranch electrosensory system. Accepted: 19 February 1998     

Sensory biology of Phalangida harvestmen (Arachnida,Opiliones): a review,with new morphological data on 18 species

Phalangida includes three of the four suborders of Opiliones (Arachnida): Eupnoi, Dyspnoi and Laniatores. We review the literature on the sensory structures and capabilities of Phalangida, provide new morphological data for 18 species and discuss the 11 sensory structures that have been described in the group. Based on the published data encompassing both behaviour and morphology, three conclusions are apparent: (1) species of Phalangida appear to have limited abilities to detect stimuli at a distance; (2) close range olfaction probably helps to find foods with strong odours, but (3) they appear to be highly dependent on contact chemoreception to detect live prey, predators and mates. We also highlight the fact that legs I in the three suborders and pedipalps in Dyspnoi and Eupnoi are very important sensory appendages, thus legs II should not be called the ‘sensory appendages’ of harvestmen. In conclusion, we highlight the fact that the sensory capabilities, diet, prey capturing and handling ability, and foraging behaviour of species of Phalangida seem to be different from those of most other arachnids. Finally, we suggest future directions for studies in the field of the sensory system of the group.     

Behavioural responses of juvenile cuttlefish (Sepia officinalis) to local water movements

Physiological studies have shown that the epidermal head and arm lines in cephalopods are a mechanoreceptive system that is similar to the fish and amphibian lateral lines (Budelmann BU, Bleckmann H. 1988. A lateral line analogue in cephalopods: Water waves generate microphonic potentials in the epidermal head lines of Sepia officinalis and Lolliguncula brevis. J. Comp. Physiol. A 164:1-5.); however, the biological significance of the epidermal lines remains unclear. To test whether cuttlefish show behavioural responses to local water movements, juvenile Sepia officinalis were exposed to local sinusoidal water movements of different frequencies (0.01-1000 Hz) produced by a vibrating sphere. Five behavioural responses were recorded: body pattern changing, moving, burrowing, orienting, and swimming. Cuttlefish responded to a wide range of frequencies (20-600 Hz), but not to all of the frequencies tested within that range. No habituation to repeated stimuli was seen. Results indicate that cuttlefish can detect local water movements (most likely with the epidermal head and arm lines) and are able to integrate that information into behavioural responses.     

Comparison of the lateral line and ampullary systems of two species of shovelnose ray

The anatomical characteristics of the mechanoreceptive lateral line system and electrosensory ampullae of Lorenzini of Rhinobatos typus and Aptychotrema rostrata are compared. The spatial distribution of somatic pores of both sensory systems is quite similar, as lateral line canals are bordered by electrosensory pore fields. Lateral line canals form a sub-epidermal, bilaterally symmetrical net on the dorsal and ventral surfaces; canals contain a nearly continuous row of sensory neuromasts along their length and are either non-pored or pored. Pored canals are connected to the surface through a single terminal pore or additionally possess numerous tubules along their length. On the dorsal surface of R. typus, all canals of the lateral line occur in the same locations as those of A. rostrata. Tubules branching off the lateral line canals of R. typus are ramified, which contrasts with the straight tubules of A. rostrata. The ventral prenasal lateral line canals of R. typus are pored and possess branched tubules in contrast to the non-pored straight canals in A. rostrata. Pores of the ampullae of Lorenzini are restricted to the cephalic region of the disk, extending only slightly onto the pectoral fins in both species. Ampullary canals penetrate subdermally and are detached from the dermis. Ampullae occur clustered together, and can be surrounded by capsules of connective tissue. We divided the somatic pores of the ampullae of Lorenzini of R. typus into 12 pore fields (10 in A. rostrata), corresponding to innervation and cluster formation. The total number of ampullary pores found on the ventral skin surface of R. typus is approximately six times higher (four times higher in A. rostrata) than dorsally. Pores are concentrated around the mouth, in the abdominal area between the gills and along the rostral cartilage. The ampullae of both species of shovelnose ray are multi-alveolate macroampullae, sensu Andres and von Düring (1988). Both the pore patterns and the distribution of the ampullary clusters in R. typus differ from A. rostrata, although a basic pore distribution pattern is conserved.     

Planktonic copepods reacting selectively to hydrodynamic disturbances

In the water column, planktonic copepods encounter small-scale hydrodynamic disturbances generated by fellow zooplankters. Our question is whether or not the copepods can distinguish between hydrodynamic disturbances created by predators, prey, conspecifics and/or mates. We used a Schlieren optical system with a density gradient in the water volume and filmed at 48 frames per second to record the behaviour of copepods during encounters with an artificial hydrodynamic disturbance. We observed the reactions of Cyclops scutifer and Epischura nordenskioldi towards disturbances of different strengths. We also re-examined an earlier report on tandem swimming in C. scutifer while attempting to mate, using novel mathematical tools to analyse possible correlations between the two mates. We conclude that the information within the hydrodynamic disturbances created by swimming zooplankters has enough content for differentiated reactions. We also suggest that the adaptive value of tandem swimming during mating results in offspring capable of executing escape reactions comparable in strength to the disturbances.     

Microstructure and mechanical properties of rostrum in Cyrtotrachelus longimanus (Coleoptera: Curculionidae)

The microstructure, composition and mechanical properties of the rostrum in Cyrtotrachelus longimanus (JHC Fabre) were studied utilizing light, fluorescent, scanning electron microscopy (SEM) and energy-dispersive spectroscopy. SEM images show the morphological characteristics of rostrum’s cross section; it is a typical lightweight multilayer structure – one rigid exocuticle layer and dense endocuticle layers, which construct unevenly overlapping fiber structures. The composition analysis of the rostrum shows that it is mainly composed of C, H, N, O, as well as some metal elements and microelements, such as Mg, Si, Zn, Ca and Na, which contribute to its mechanical performance. The mechanical properties of the rostrum were tested by the electronic universal testing machine, which shows it has high-specific strength and is almost the same as that of the stainless steel. The results may provide a biological template to inspire biomimetic lightweight structure design.     

Rotatory apparatus in Bdelloids

All Bdelloid Rotifers have the same body plan: elongated body, ciliated apical region (rotatory apparatus or corona), telescopically retractable foot and head with pseudosegments, paired gonads, single dorsal antenna, apical rostrum, ramate mastax. Bdelloids use the rotatory apparatus for both locomotion and collecting food and therefore the shape of the corona and arrangement of the cilia, both related to the animal's life style, probably are important for the fitness of the rotifers. We have analyzed the fine morphology of the corona and the rostrum from species belonging to the four families, Habrotrochidae, Philodinidae, Adinetidae and Philodinavidae, each with its own form of feeding and locomotion. In the rostrum one can distinguish a sensorial area and a ciliated area. The former is common to all bdelloids, while the latter is lacking in the Adinetidae. Three models of corona can be recognized: 1) a simple ciliated field of undifferentiated cilia (Adinetidae), 2) a well developed ciliated field with specialized cilia forming the paired trochi on the disks and the cingulum (Habrotrochidae and Philodinidae), and 3) a ciliated field with a single trochus encompassing rudimentary pedicels and cingulum (Abrochtha). We propose (1) to no longer use Digononta as a taxon, (2) to assign the class rank to Bdelloidea, (3) to distinguish three orders, grouping Philodinidae and Habrotrochidae under a single order and (4) to retain the current families.