Triakis Semifasciata Research Articles

Seasonal, interannual, and long-term variation in sport fish contamination, San Francisco Bay

This study documents changes in contamination over time at seasonal, interannual, and decadal time scales for sport fish collected in San Francisco Bay. Samples from seven fish species were prepared according to common consumption practices (muscle fillets either with or without skin) and analyzed for trace metals (mercury and selenium) and trace organochlorine contaminants (PCBs, DDTs, chlordanes, and dieldrin). In 2000, sport fish samples exceeded human health screening values for mercury, PCBs, DDTs, selenium, and dieldrin but did not exceed screening values for chlordanes. On a seasonal time scale, white croaker ( Genyonemus lineatus) exhibited significantly lower PCB and lipid concentrations in spring, and a general increase in concentrations in other seasons. When monitoring data were compared among 1994, 1997, and 2000, analysis of variance indicated that concentrations of mercury, PCBs, DDTs, and chlordanes varied significantly among years for several fish species. Interannual variation in DDTs often correlated to changes in sampled fish size or lipid content among years. Interannual variation in mercury and PCBs was evident in striped bass ( Morone saxatilis) but absent in shiner surfperch ( Cymatogaster aggregata), leopard shark ( Triakis semifasciata), and white croaker. The higher interannual variability of striped bass contaminant concentrations may result from migratory behavior and wide home ranges. Chlordanes significantly declined between 1994 and 2000 in white croaker and striped bass. Of the historical data analyzed (1986–2000), only DDT concentrations in white sturgeon ( Acipenser transmontanus) showed evidence of a significant decline. Neither PCBs nor selenium showed evidence of a trend in white sturgeon. Between 1970 and 2000, mercury concentrations in striped bass showed no evidence of a trend. The absence of recent trends in mercury may result from the presence of widespread and historic sources, with use reductions occurring in the early 20th century. In contrast to mercury, apparent recent declines in fish tissue DDT and chlordane concentrations may result from use curtailment in the 1970s and 1980s.

Steady swimming muscle dynamics in the leopard sharkTriakis semifasciata

Patterns of red muscle strain and activation were examined at three positions along the body (0.42, 0.61 and 0.72 L, where L is total body length) and correlated with simultaneous measurements of midline kinematics during steady swimming (approx. 1.0 L s(-1)) in the leopard shark Triakis semifasciata. Analysis of lateral displacement along the body indicates that the leopard shark is a subcarangiform swimmer. Longitudinal variation in red muscle strain was observed with strain amplitudes ranging from +/-3.9% in the anterior, +/-6.6% in the mid, to +/-4.8% in the posterior body position. Strain was in-phase with local midline curvature. In addition, strain amplitude calculated from a bending beam model closely matched strain measured using sonomicrometry at all three body positions. There is a high degree of similarity in red muscle activation patterns along the body between the leopard shark and many fish species, in that the onset of activation occurs during muscle lengthening while offset occurs during muscle shortening. However, we found no significant longitudinal variation in the EMG/strain phase relationship and duty cycles, with onset of muscle activation occurring at 51.4-61.8 degrees and offset at 159.7-165.2 degrees (90 degrees is peak length). This consistent pattern of activation suggests that red muscle along the entire length of the body contributes to positive power production. Thus, sharks such as Triakis may have no regional specialization in red muscle function like that seen in many teleosts, which may indicate that the evolution of differential muscle function along the body occurred after the divergence of cartilaginous and bony fishes.

The Influence of Environmental Variables on the Distribution and Abundance of Three Elasmobranchs in Tomales Bay, California

We tested the hypothesis that temperature, salinity, and dissolved oxygen affect elasmobranch distribution and abundance in Tomales Bay, California, with monthly longline samples over a 20 month period. We used a Poisson regression under generalized least squares and found that temperature and salinity were the most important factors determining the distribution and abundance of the three most common elasmobranch species, bat ray, Myliobatis californica, leopard shark, Triakis semifasciata, and brown smoothhound shark, Mustelis henlei. Females of all three species were more abundant than males throughout the Bay, and were most abundant in the warmer, more saline inner bay. All three species apparently left Tomales Bay in late fall as water temperatures in the bay decreased to 10° C. Three of 257 bat rays tagged in Tomales Bay were recaptured, all within 1 km of their tagging location despite having been free for up to 583 d.

Effect of Temperature on Oxygen Consumption of the Leopard Shark, Triakis Semifasciata

The leopard shark, Triakis semifasciata, regularly resides in California's Tomales Bay, which is characterized by thermally different regions ranging from 10°C to 26°C during the summer. Past studies have shown that leopard sharks feed on benthic invertebrate prey similar to that of the sympatric bat ray, Myliobatis californica. Fishes' metabolic (oxygen consumption) rates typically increase with temperature increases, and we measured leopard sharks' metabolic responses and sensitivity to ambient temperature, using flow-through respirometry. Leopard shark oxygen consumption rate increased with increasing temperature, over a range of 12–24°C, with a typical temperature sensitivity (Q10 = 2.51). Whereas bat rays use a highly temperature-sensitive metabolism to efficiently feed (in warmer waters) and digest (in cooler waters) during different phases of the diel cycle, leopard sharks possess a more typical metabolic temperature sensitivity that allows for high-tide foraging, throughout the diel cycle.

Function of the heterocercal tail in sharks: quantitative wake dynamics during steady horizontal swimming and vertical maneuvering.

The function of the heterocercal tail in sharks has long been debated in the literature. Previous kinematic data have supported the classical theory which proposes that the beating of the heterocercal caudal fin during steady horizontal locomotion pushes posteroventrally on the water, generating a reactive force directed anterodorsally and causing rotation around the center of mass. An alternative model suggests that the heterocercal shark tail functions to direct reaction forces through the center of mass. In this paper, we quantify the function of the tail in two species of shark and compare shark tail function with previous hydrodynamic data on the heterocercal tail of sturgeon Acipenser transmontanus. To address the two models of shark heterocercal tail function, we applied the technique of digital particle image velocimetry (DPIV) to quantify the wake of two species of shark swimming in a flow tank. Both steady horizontal locomotion and vertical maneuvering were analyzed. We used DPIV with both horizontal and vertical light sheet orientations to quantify patterns of wake velocity and vorticity behind the heterocercal tail of leopard sharks (Triakis semifasciata) and bamboo sharks (Chiloscyllium punctatum) swimming at 1.0Ls(-1), where L is total body length. Two synchronized high-speed video cameras allowed simultaneous measurement of shark body position and wake structure. We measured the orientation of tail vortices shed into the wake and the orientation of the central jet through the core of these vortices relative to body orientation. Analysis of flow geometry indicates that the tail of both leopard and bamboo shark generates strongly tilted vortex rings with a mean jet angle of approximately 30 degrees below horizontal during steady horizontal swimming. The corresponding angle of the reaction force is much greater than body angle (mean 11 degrees ) and the angle of the path of motion of the center of mass (mean approximately 0 degrees ), thus strongly supporting the classical model of heterocercal tail function for steady horizontal locomotion. Vortex jet angle varies significantly with body angle changes during vertical maneuvering, but sharks show no evidence of active reorientation of jet angle relative to body angle, as was seen in a previous study on the function of sturgeon tail. Vortex jet orientation is significantly more inclined than the relatively horizontal jet generated by sturgeon tail vortex rings, demonstrating substantial differences in function in the heterocercal tails of sharks and sturgeon. We present a summary of forces on a swimming shark integrating data obtained here on the tail with previous data on pectoral fin and body function. Body orientation plays a critical role in the overall force balance and compensates for torques generated by the tail. The pectoral fins do not generate lift during steady horizontal locomotion, but play an important hydrodynamic role during vertical maneuvering.

Contaminant concentrations in sport fish from San Francisco Bay, 1997

In 1997, seven sport fish species were sampled from seven popular fishing areas in San Francisco Bay. Mercury exceeded a human health screening value in 44 of 84 (52%) samples. All collected samples of leopard shark and striped bass exceeded the mercury screening value of 0.23 μg/g wet weight. PCBs exceeded the screening value in 51 of 72 (71%) samples. DDT, chlordane, and dieldrin, had lower numbers of samples above screening values: 16 of 72 (22%) for DDT, 11 of 72 (15%) for chlordanes, and 27 of 72 (37%) for dieldrin. Concentrations of PCBs and other trace organics were highest in white croaker and shiner surfperch, the two species with the highest fat content in their muscle tissue. Fish from one location, Oakland Harbor, had significantly elevated wet weight concentrations of mercury, PCBs, DDTs, and chlordanes compared to other locations. Removal of skin from white croaker fillets reduced lipid concentrations by 27–49% and concentrations of trace organics by 33–40%.

Functional morphology of the pectoral fins in bamboo sharks, Chiloscyllium plagiosum: benthic vs. pelagic station-holding.

Bamboo sharks (Chiloscyllium plagiosum) are primarily benthic and use their relatively flexible pectoral and pelvic fins to rest on and move about the substrate. We examined the morphology of the pectoral fins and investigated their locomotory function to determine if pectoral fin function during both benthic station-holding and pelagic swimming differs from fin function described previously in leopard sharks, Triakis semifasciata. We used three-dimensional kinematics and digital particle image velocimetry (DPIV) to quantify pectoral fin function in five white-spotted bamboo sharks, C. plagiosum, during four behaviors: holding station on the substrate, steady horizontal swimming, and rising and sinking during swimming. During benthic station-holding in current flow, bamboo sharks decrease body angle and adjust pectoral fin angle to shed a clockwise fluid vortex. This vortex generates negative lift more than eight times that produced during open water vertical maneuvering and also results in an upstream flow that pushes against the posterior surface of the pectoral fin to oppose drag. In contrast, there is no evidence of significant lift force in the wake of the pectoral fin during steady horizontal swimming. The pectoral fin is held concave downward and at a negative dihedral angle during steady horizontal swimming, promoting maneuverability rather than stability, although this negative dihedral angle is much less than that observed previously in sturgeon and leopard sharks. During sinking, the pectoral fins are held concave upward and shed a clockwise vortex with a negative lift force, while in rising the pectoral fin is held concave downward and sheds a counterclockwise vortex with a positive lift force. Bamboo sharks appear to sacrifice maneuverability for stability when locomoting in the water column and use their relatively flexible fins to generate strong negative lift forces when holding position on the substrate and to enhance stability when swimming in the water column.

Three-dimensional kinematics and wake structure of the pectoral fins during locomotion in leopard sharks Triakis semifasciata.

The classical theory of locomotion in sharks proposes that shark pectoral fins are oriented to generate lift forces that balance the moment produced by the oscillating heterocercal tail. Accordingly, previous studies of shark locomotion have used fixed-wing aircraft as a model assuming that sharks have similar stability and control mechanisms. However, unlike airplanes, sharks are propelled by undulations of the body and tail and have considerable control of pectoral fin motion. In this paper, we use a new approach to examine the function of the pectoral fins of leopard sharks, Triakis semifasciata, during steady horizontal swimming at speeds of 0.5-2.0ls(-1), where l is total body length, and during vertical maneuvering (rising and sinking) in the water column. The planar orientation of the pectoral fin was measured using three-dimensional kinematics, while fluid flow in the wake of the pectoral fin and forces exerted on the water by the fin were quantified using digital particle image velocimetry (DPIV). Steady horizontal swimming in leopard sharks is characterized by continuous undulations of the body with a positive body tilt to the flow that decreases from a mean of 11 degrees to 0.6 degrees with increasing flow speeds from 0. 5 to 2.0ls(-1). Three-dimensional analysis showed that, during steady horizontal locomotion, the pectoral fins are cambered, concave downwards, at a negative angle of attack that we predict to generate no significant lift. Leopard shark pectoral fins are also oriented at a substantial negative dihedral angle that amplifies roll moments and hence promotes rapid changes in body position. Vortices shed from the trailing edge of the pectoral fin were detected only during vertical maneuvering. Starting vortices are produced when the posterior plane of the pectoral fin is actively flipped upwards or downwards to initiate rising or sinking, respectively, in the water column. The starting vortex produced by the pectoral fin induces a pitching moment that reorients the body relative to the flow. Body and pectoral fin surface angle are altered significantly when leopard sharks change vertical position in the water column. Thus, locomotion in leopard sharks is not analogous to flight in fixed-wing aircraft. Instead, a new force balance for swimming leopard sharks is proposed for steady swimming and maneuvering. Total force balance on the body is adjusted by altering the body angle during steady swimming as well as during vertical maneuvering, while the pectoral fins appear to be critical for initiating maneuvering behaviors, but not for lift production during steady horizontal locomotion.

The role of the pectoral fins in body trim of sharks

In a large aquarium the leopard shark Triakis semifasciata, sand tiger shark Odontaspis taurus, sandbar shark Carcharhinus plumbeus, and spiny dogfish Squalus acanthias cruised steadily at 0·1‐0·7 body lengths s‐1. Relative to the trajectory of the shark, the pectoral fins were maintained at a positive angle of ttack regardless of vertical direction. For level swimming the mean angle of attack for the pectoral fin was 11±1·7, 10·1±1·3°, 9·3±1·3°, and 15·0±0·0 for T. semifasciata, C. plumbeus, O. taurus, and S. acanthias, respectively. The long axis of the body was canted at an angle of attack for T. semifasciata and S. acanthias, but trim was maintained during level swimming for C. plumbeus and O. taurus. Hydrodynamic analysis of the body and fin design of T. semifasciata indicated that the pectoral fins could develop suffcient pitching moment to maintain depth and keep the body in trim. Demonstration of positive angles of attack support the hypothesis that lift is generated in the anterior body to counterbalance the lift produced by the heterocercal tail.

Function of the Caudal Fin During Locomotion in Fishes: Kinematics, Flow Visualization, and Evolutionary Patterns1

One of the most prominent characteristics of early vertebrates is the elongate caudal fin bearing fin rays. The caudal fin represents a fundamental design feature of vertebrates that predates the origin of jaws and is found in both agnathans and gnathostomes. The caudal fin also represents the most posterior region of the vertebrate axis and is the location where fluid, accelerated by movement of the body anteriorly, is shed into the surrounding medium. Despite the extensive fossil record of the caudal fin, the use of caudal characters for systematic studies, and the importance of tail function for understanding locomotor dynamics in fishes, few experimental studies have been undertaken of caudal fin function. In this paper I review two experimental approaches which promise to provide new insights into the function and evolution of the caudal fin: three-dimensional kinematic analysis, and quantitative flow measurements in the wake of freely-swimming fishes using digital particle image velocimetry (DPIV). These methods are then applied to the function of the caudal fin during steady swimming in fishes with heterocercal and homocercal morphologies: chondrichthyians (leopard sharks) and ray-fined fishes (sturgeon and bluegill sunfish). The caudal fin of leopard sharks functions in a manner consistent with the classical model of heterocercal tail function in which the caudal surface moves at an acute angle to the horizontal plane, and hence is expected to generate lift forces and torques which must be counteracted anteriorly by the body and pectoral fins. An alternative model in which the shark tail produces a reactive force that acts through the center of mass is not supported. The sturgeon heterocercal tail is extremely flexible and the upper tail lobe trails the lower during the fin beat cycle. The sturgeon tail does not function according to the classical model of the heterocercal tail, and is hypothesized to generate reactive forces oriented near the center of mass of the body which is tilted at an angle to the flow during steady locomotion. Functional analysis of the homocercal tail of bluegill shows that the dorsal and ventral lobes do not function symmetrically as expected. Rather, the dorsal lobe undergoes greater lateral excursions and moves at higher velocities than the ventral lobe. The surface of the dorsal lobe also achieves a significantly acute angle to the horizontal plane suggesting that the homocercal tail of bluegill generates lift during steady swimming. These movements are actively generated by the hypochordal longitudinalis muscle within the tail. This result, combined with DPIV flow visualization data, suggest a new hypothesis for the function of the homocercal tail: the homocercal tail generates tilted and linked vortex rings with a central jet inclined posteroventrally, producing an anterodorsal reactive force on the body which generates lift and torque in the manner expected of a heterocercal tail. These results show that the application of new techniques to the study of caudal fin function in fishes reveals a previously unknown diversity of homocercal and heterocercal tail function, and that morphological characterizations of caudal fins do not accurately reflect in vivo function.

Function of the Caudal Fin During Locomotion in Fishes: Kinematics, Flow Visualization, and Evolutionary Patterns

One of the most prominent characteristics of early vertebrates is the elongate caudal fin bearing fin rays. The caudal fin represents a fundamental design feature of vertebrates that predates the origin of jaws and is found in both agnathans and gnathostomes. The caudal fin also represents the most posterior region of the vertebrate axis and is the location where fluid, accelerated by movement of the body anteriorly, is shed into the surrounding medium. Despite the extensive fossil record of the caudal fin, the use of caudal characters for systematic studies, and the importance of tail function for understanding locomotor dynamics in fishes, few experimental studies have been undertaken of caudal fin function. In this paper I review two experimental approaches which promise to provide new insights into the function and evolution of the caudal fin: three-dimensional kinematic analysis, and quantitative flow measurements in the wake of freely-swimming fishes using digital particle image velocimetry (DPIV). These methods are then applied to the function of the caudal fin during steady swimming in fishes with heterocercal and homocercal morphologies: chondrichthyians (leopard sharks) and ray-fined fishes (sturgeon and bluegill sunfish). The caudal fin of leopard sharks functions in a manner consistent with the classical model of heterocercal tail function in which the caudal surface moves at an acute angle to the horizontal plane, and hence is expected to generate lift forces and torques which must be counteracted anteriorly by the body and pectoral fins. An alternative model in which the shark tail produces a reactive force that acts through the center of mass is not supported. The sturgeon heterocercal tail is extremely flexible and the upper tail lobe trails the lower during the fin beat cycle. The sturgeon tail does not function according to the classical model of the heterocercal tail, and is hypothesized to generate reactive forces oriented near the center of mass of the body which is tilted at an angle to the flow during steady locomotion. Functional analysis of the homocercal tail of bluegill shows that the dorsal and ventral lobes do not function symmetrically as expected. Rather, the dorsal lobe undergoes greater lateral excursions and moves at higher velocities than the ventral lobe. The surface of the dorsal lobe also achieves a significantly acute angle to the horizontal plane suggesting that the homocercal tail of bluegill generates lift during steady swimming. These movements are actively generated by the hypochordal longitudinalis muscle within the tail. This result, combined with DPIV flow visualization data, suggest a new hypothesis for the function of the homocercal tail: the homocercal tail generates tilted and linked vortex rings with a central jet inclined posteroventrally, producing an anterodorsal reactive force on the body which generates lift and torque in the manner expected of a heterocercal tail. These results show that the application of new techniques to the study of caudal fin function in fishes reveals a previously unknown diversity of homocercal and heterocercal tail function, and that morphological characterizations of caudal fins do not accurately reflect in vivo function.

Tidal Influence on Spatial Dynamics of Leopard Sharks, Triakis semifasciata, in Tomales Bay, California

We used ultrasonic telemetry to determine the movement directions and movement rates of leopard sharks, Triakis semifasciata, in Tomales Bay, California. To analyze tide and time of day effects, we surgically implanted transmitters in the peritoneal cavities of one male and five female leopard sharks, which we located during summer for three to five sampling sessions lasting 12 to 24 h each. All leopard sharks showed strong movement direction patterns with tide. During incoming tides, sharks moved significantly (p<0.0001) towards the inner bay, apparently to exploit the extensive inner bay muddy littoral zones' food resources. On outgoing tides, sharks showed significant (p<0.0001) movements towards the outer bay. During high tide, there was no discernible pattern to their movements (p=0.092). Shark movement rates were significantly (p<0.0001) greater during dark periods (mean±SE: 10.5±1.0 m min−1), compared with fully lighted ones (6.7±0.5 m min−1). Movement rates of longer sharks tended to be greater than those of shorter ones (range means±SE: 5.8±0.6 m min−1 for the 91 cm shark, to 12.8±1.6 m min−1 for the 119 cm shark), but the leopard sharks' overall mean movement rate (8.1±0.5 m min−1) was slower than other (more pelagic) sharks.

Effects of prey size and mobility on prey-capture kinematics in leopard sharks triakis semifasciata

Recent work on teleosts suggests that attack behaviors or kinematics may be modified by a predator on the basis of the size of the prey or the ability of the prey to sense predators and escape capture (elusivity). Sharks are generally presumed to be highly visual predators; thus, it is reasonable to expect that they might also be capable of such behavioral modulation. In this study, I investigated the effect of prey item size and type on prey-capture behavior in leopard sharks (Triakis semifasciata) that had been acclimated to feeding in the laboratory. Using high-speed video, sharks were filmed feeding on two sizes of the same prey item (thawed shrimp pieces) and two potentially more elusive prey items (live earthworms and live mud shrimp). In leopard sharks, little effect of prey elusivity was found for kinematic variables during prey capture. However, the large proportion of successful captures of the live prey suggests that they did not prove to be truly elusive prey items for the leopard shark. There were significant size effects on prey-capture kinematics, with the larger non-elusive items inducing greater head expansion during prey capture. Ram-suction index values also indicated that strikes on large, non-elusive prey had a significantly larger suction component than strikes on similar small prey items. This finding is interesting given that the two sizes of non-elusive prey item offered no differential challenge in terms of a performance consequence (reduced capture success).

A new device for monitoring gastric pH in free-ranging animals.

An autonomous stomach probe for the measurement of gastric pH and temperature in free-ranging animals is presented. The probe was successfully deployed in four species of penguins and measured pH for periods of up to 10 days under fluctuating pressure conditions. The resolution of pH was better than 0.1 pH units, and the absolute accuracy was on average better than 0.25 pH units for deployment in Pygoscelis penguins and better than 0.1 pH units in Spheniscus penguins. Stomach pH in chickrearing penguins was highly flexible, with values ranging from below pH 2 to virtually neutral, allowing the birds to adjust the rate of digestion to the prevailing demands.

A "Good-Sperm" Model Can Explain the Evolution of Costly Multiple Mating by Females

A "Good-Sperm" Model Can Explain the Evolution of Costly Multiple Mating by Females

A demographic method with population density compensation for estimating productivity and yield per recruit of the leopard shark (Triakis semifasciata)

On montre une methode, en prenant pour exemple le requin-tigre (Triakis semifasciata), pour obtenir des valeurs estimees du taux d'augmentation intrinseque d'une population (r) qui depend du degre de mortalite total eprouve. La methode utilise l'âge de maturite de la femelle, l'âge de reproduction maximal et la fertilite moyenne et incorpore des concepts de dependance a l'egard de la densite tires de la modelisation standard des populations de poissons. Une estimation de la valeur r du requin-tigre pour la taille de la population produisant le rendement maximal durable a ainsi ete obtenue, puis etendue pour ajuster les valeurs estimees de son rendement par recrue pour tenir compte des effets de la reduction du recrutement attribuable a la peche. Les resultats indiquent que ce requin pourrait etre plus vulnerable a la surpeche qu'on le croyait jusqu'ici. On a montre que cette methode est capable de donner des valeurs r pour le requin-tigre et cinq autres especes de requins qui se comparent favorablement avec les valeurs publiees obtenues par la methode plus traditionnelle des tables de survie. Elle devrait s'averer utile pour evaluer l'etat des populations pour lesquelles il existe peu de donnees.

A demographic method with population density compensation for estimating productivity and yield per recruit of the leopard shark (&lt;I&gt;Triakis semifasciata&lt;/I&gt;)

A demographic method with population density compensation for estimating productivity and yield per recruit of the leopard shark (&lt;I&gt;Triakis semifasciata&lt;/I&gt;)

Heterocercal tail function in leopard sharks: a three-dimensional kinematic analysis of two models

Two different models have been proposed to explain the function of the heterocercal tail in shark locomotion. The classical model proposes that, as a result of lift generated by the tail as it beats, the net force acting on the tail is directed dorsally and anteriorly. In contrast, Thomson's model suggests that the tail generates a net force directed through the shark's center of gravity, i.e. ventrally and anteriorly. In this study, we evaluate these two models by describing the three-dimensional kinematics of the heterocercal tail in the leopard shark Triakis semifasciata during swimming. Lateral and posterior views of the tail were examined from four individuals swimming in a flow tank at 1.2 L s-1 (where L is total length) using two high-speed video cameras filming simultaneously at 250 fields s-1. These two simultaneous views allowed eight landmarks on the tail to be followed in three dimensions through time. These landmarks allowed the tail to be divided into separate surfaces whose orientation over time was calculated. Points located anteriorly on the tail go through significantly smaller excursions and reach their maximum lateral excursion significantly earlier in the beat cycle than points on the trailing edge of the tail. Three-dimensional angle calculations show that the terminal lobe leads the ventral lobe through a beat, as predicted by the classical model. Dye-stream visualizations confirmed that this pattern of movement deflects water ventrally and posteriorly to the moving tail, providing strong support for the classical model. Additionally, our results show that a three-dimensional analysis is critical to understanding the function of the heterocercal tail.

Visual pigments and photoreceptors in two species of shark,Triakis semifasciata andMustelus henlei

The retinal photoreceptors of brown smoothhound sharks (Mustelus henlei) and leopard sharks (Triakis semifasciata) were studied by spectrophotometric analysis of visual pigment extracts, microspectrophotometric examination of single cells, and scanning electron microscopy. Juvenile and adult brown smoothhounds have one, identical visual pigment in their rod photoreceptors. The visual pigment is based on the vitamin A1 chromophore and has a peak absorbance (λmax) (at 496 ± 2 nm. Juvenile and adult leopard sharks also have a single, vitamin A1 based visual pigment, this one with λmax at 502 ± 1 nm. No evidence was found for a shift from a vitamin A2 based visual pigment in the juveniles to a vitamin A1 based pigment in the adults, as is known to occur in the lemon shark, Negaprion brevirostris (Cohen et al. [1990] Vision Res., 30:1949–1953). The retinas of brown smoothhounds and leopard sharks contain both rods and cones, with the rods dominating. The rod outer segments of the brown smoothhound are much longer than are those of the leopard shark. The greater length of brown smoothhound rod outer segments and the shorter wavelength λmax of the brown smoothhound's rod pigment support the idea that brown smoothhounds are either more nocturnal than leopard sharks or are active at greater depths. Cones are very rare in both species with only three identified with the scanning electron microscope and none with the microspectrophotometer. The apparent paucity of cones most likely relates to the bottom dwelling lifestyle of these sharks, although the possibility remains that their retinas contain small, specialized regions of high cone density, which were simply missed. © 1996 Wiley-Liss, Inc.

Tonic immobility in 12 elasmobranchs: Use as an aid in captive husbandry

AbstractTonic immobility (TI), also known as animal hypnosis, has been observed in a wide variety of taxa and reported in all vertebrate classes with the exception of Agnatha. To date, TI has been reported in six species of elasmobranchs. Preliminary results are presented here for five species of galeomorph sharks, one species of squalomorph shark, and six species of batoids. Tonic immobility was induced in the leopard shark. Triakis semifasciata; the whitetip reef shark, Triaenodon obesus; the blacktip reef shark, Carcharhinus melanopterus; the Caribbean reef shark, Carcharhinus perezi; the swellshark, Cephaloscyllium ventriosum; the California round ray, Urolophus halleri; the shovelnose guitarfish, Rhinobatos productus; the clearnose skate. Raja eglanteria; the cownose ray, Rhinoptera bonasus; and the southern stingray, Dasyatis americana. The broadnose sevengill shark, Notorynchus cepedianus and the yellow stingray, Urolophus jamaicensis failed to exhibit the tonic immobility response, but only one individual of each species was tested. The average induction time ranged from 16.7 sec in the shovelnose guitarfish to 45.7 sec in the clearnose skate. Average duration times ranged from 34.3 sec in the clearnose skate to 274.0 sec in the Caribbean reef shark. Depending upon the species involved, TI has been used as an aid in a few husbandry and medical procedures in captive elasmobranches at the National Aquarium in Baltimore. These procedures have included gross examination, measuring lengths, tube feeding, and drawing blood via caudal venipuncture. Using tonic immobility during these procedures is beneficial as once induced, the subject's struggling is minimal and usually requires little restraint. © 1994 Wiley‐Liss, Inc.