Comparative feeding ecology of the yellow ray Urobatis jamaicensis (Urotrygonidae) from The Bahamas

Stomach contents were collected from 117 yellow rays Urobatis jamaicensis from three locations in south Eleuthera, The Bahamas and compared with ambient infauna via sediment surveys. Diets were relatively limited with a total of 535 prey items recovered, representing five taxonomic groups and dominated by polychaetes and decapod crustaceans (87% of total diet), while environmental sampling reported 5249 individual taxa represented by 62 taxonomic groups. Regardless of gravidity, sex or density of prey items among sites, no significant differences were detected. Foraging strategy plots suggested preferential prey is rare within the environment and the Manly‐Chesson index validates polychaetes were consumed with high selectivity. This is the most comprehensive and updated assessment of comparative feeding in this species, particularly for The Bahamas, allowing insight into invertebrate community richness and diversity in ecologically sensitive coastal and nearshore habitats.     

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.     

Annual breeding in a captive smalltooth sawfish,Pristis pectinata

The critically endangered smalltooth sawfish Pristis pectinata reproduces biennially in central west Florida, U.S.A. Here we demonstrate that smalltooth sawfish are physiologically capable of reproducing annually in a captive environment. The smalltooth sawfish are held in an open system, with abiotic conditions that vary naturally with the surrounding environment in The Bahamas. This suggests wild smalltooth sawfish may also be capable of annual reproduction provided there are adequate prey resources, limited competition and mate availability.     

Life history of the cownose ray, <Emphasis Type="Italic">Rhinoptera bonasus</Emphasis>, in the northern Gulf of Mexico,with comments on geographic variability in life history traits

Synopsis We determined age and growth, size at maturity, and fecundity for cownose rays, Rhinoptera bonasus, collected from the northern Gulf of Mexico. Vertebral age estimates ranged from 0+ to 18+ years for females and 0+ to 16+ years for males. Annual deposition of growth increments was verified with marginal increment analysis. Likelihood ratio tests indicated that the growth of the cownose ray was best described by a combined sexes Gompertz model. Median size at 50% maturity was determined to be 642 mm DW for males and 653 mm DW for females, or 4–5 years of age. Median pup size-at-birth was estimated to be 350 mm DW, with a gestation period of 11–12 months. In all cases, gravid females contained only one pup. Statistically significant differences were detected between growth curves for the Gulf of Mexico and the western Atlantic Ocean. Cownose rays in the Gulf of Mexico had lower estimates of DW_∞ and K, and a higher theoretical longevity than their conspecifics in the western Atlantic Ocean. Cownose rays in the Gulf of Mexico also attain maturity at a smaller size and earlier age than their counterparts in the western Atlantic Ocean.     

Comparative morphology of stingray lateral line canal and electrosensory systems

Elasmobranchs (sharks, skates, and rays) possess a variety of sensory systems including the mechanosensory lateral line and electrosensory systems, which are particularly complex with high levels of interspecific variation in batoids (skates and rays). Rays have dorsoventrally compressed, laterally expanded bodies that prevent them from seeing their mouths and more often than not, their prey. This study uses quantitative image analysis techniques to identify, quantify, and compare structural differences that may have functional consequences in the detection capabilities of three Eastern Pacific stingray species. The benthic round stingray, Urobatis halleri, pelagic stingray, Pteroplatytrygon (Dasyatis) violacea, and benthopelagic bat ray, Myliobatis californica, show significant differences in sensory morphology. Ventral lateral line canals correlate with feeding ecology and differ primarily in the proportion of pored and nonpored canals and the degree of branching complexity. Urobatis halleri shows a high proportion of nonpored canals, while P. violacea has an intermediate proportion of pored and nonpored canals with almost no secondary branching of pored canals. In contrast, M. californica has extensive and highly branched pored ventral lateral line canals that extended laterally toward the wing tips on the anterior edge of the pectoral fins. Electrosensory morphology correlates with feeding habitat and prey mobility; benthic feeders U. halleri and M. californica, have greater electrosensory pore numbers and densities than P. violacea. The percentage of the wing surface covered by these sensory systems appears to be inversely related to swimming style. These methods can be applied to a broader range of species to enable further discussion of the relationship of phylogeny, ecology, and morphology, while the results provide testable predictions of detection capabilities. J. Morphol., 2008. © 2008 Wiley‐Liss, Inc.     

Paleobiology of the Late Cretaceous sclerorhynchid sawfish,Ischyrhiza mira (Elasmobranchii: Rajiformes), from North America based on new anatomical data

Abstract

We describe seven associated skeletal remains of Ischyrhiza mira, a Late Cretaceous sclerorhynchid sawfish, from the Campanian?lower Maastrichtian of Tennessee and Alabama, U.S.A., to decipher its paleobiology. Ischyrhiza mira had about 16 or 17 functional spines and about the same number of replacement spines on each side of the rostrum in which tall erect spines occupied the anterior one-half to two-third of the rostrum followed posteriorly by smaller spines. Whereas small hat-shaped dermal denticles were distributed on the rostrum, large thorn-like dermal denticles were present on the dorsal side of the body characteristic of sluggish, benthic batoids. We concur with the interpretation that specimens previously identified as rostral spines of Peyeria are actually enlarged thorn-like dermal denticles of a sclerorhynchid. We suggest that the ratio between the rostrum length and total body length of sclerorhynchids was generally about 1:3.27. Our vertebra-based ontogenetic analysis of I. mira gives an age estimate of 12.4 years for a 190-cm-long individual, the size at birth of about 0.5 m, and the maximum possible length for the species of no more than 3 m. Compared to extant pristid sawfishes, I. mira probably became sexually mature much earlier with a slightly faster rate of rostrum development.     

A new genus and species of fossil myliobatoid ray from the Fishburne Formation (lower Eocene/Ypresian) of Berkeley County,South Carolina,USA

Elasmobranch fossils recovered from the Fishburne Formation (lower Eocene/Ypresian) of Berkeley County, South Carolina, USA, include species from four genera of sharks and six genera of rays. Of particular interest was the recovery of multiple isolated teeth from a new genus and species of the cownosed ray family Rhinopteridae, which is the focus of this study. The unique crown morphology separates this genus and species from Rhinoptera. Eorhinoptera grabdai, gen. et sp. nov., is represented by small, bar-shaped teeth in the shape of greatly elongated hexagons. These teeth are the isolated elements of a dental plate. The holotype, with 12 wide root lobes, is the most elongated in the sample being 1 cm long and 1.5 mm wide, indicating an origin in the central region of the plate. Paratypes are less elongated, have 4–8 root lobes and are from more lateral rows. The crown is smooth and has a distinctly convex occlusal surface. Eorhinoptera is only the second genus of cow-nosed ray. Its distinctive crown morphology may have allowed it to exploit different kinds of prey than those favoured by rays that lacked convex tooth crowns.     

Site affinity of whitespotted eagle rays Aetobatus narinari assessed using photographic identification

Photographic identification was used to track the movements of the whitespotted eagle ray Aetobatus narinari around South Caicos, Turks and Caicos Islands. A total of 165 individuals were identified, aided by the computer program I³S Spot. The sex ratio across all study sites in 2015 was not significantly different from 1:1 (χ² = 2·8, P > 0·05). 33·9% of all individual rays were resighted at least once and the maximum number of days between the first and last sighting was 1640 (median 165, interquartile range, IQR = 698). Sightings of individuals occurred at locations differing from the original sighting location 24·6% of the time (0·7–20 km away). The entire population around South Caicos has yet to be sampled and these rays exhibited site affinity during the study period; they are either resident to South Caicos or are using the area for parts of the year before making movements elsewhere and then returning. Given these results, A. narinari is suited to local‐scale management and conservation efforts.     

Morphology of the Mechanosensory Lateral Line System in Elasmobranch Fishes: Ecological and Behavioral Considerations

The relationship between morphology of the mechanosensory lateral line system and behavior is essentially unknown in elasmobranch fishes. Gross anatomy and spatial distribution of different peripheral lateral line components were examined in several batoids (Raja eglanteria, Narcine brasiliensis, Gymnura micrura, and Dasyatis sabina) and a bonnethead shark, Sphyrna tiburo, and are interpreted to infer possible behavioral functions for superficial neuromasts, canals, and vesicles of Savi in these species. Narcine brasiliensis has canals on the dorsal surface with 1 pore per tubule branch, lacks a ventral canal system, and has 8–10 vesicles of Savi in bilateral rows on the dorsal rostrum and numerous vesicles ( = 65 ± 6 SD per side) on the ventral rostrum. Raja eglanteria has superficial neuromasts in bilateral rows along the dorsal body midline and tail, a pair anterior to each endolymphatic pore, and a row of 5–6 between the infraorbital canal and eye. Raja eglanteria also has dorsal canals with 1 pore per tubule branch, pored and non-pored canals on the ventral surface, and lacks a ventral subpleural loop. Gymnura micrura has a pored dorsal canal system with extensive branch patterns, a pored ventral hyomandibular canal, and non-pored canal sections around the mouth. Dasyatis sabina has more canal pores on the dorsal body surface, but more canal neuromasts and greater diameter canals on the ventral surface. Sphyrna tiburo has primarily pored canals on both the dorsal and ventral surfaces of the head, as well as the posterior lateral line canal along the lateral body surface. Based upon these morphological data, pored canals on the dorsal body and tail of elasmobranchs are best positioned to detect water movements across the body surface generated by currents, predators, conspecifics, or distortions in the animal's flow field while swimming. In addition, pored canals on the ventral surface likely also detect water movements generated by prey. Superficial neuromasts are protected from stimulation caused by forward swimming motion by their position at the base of papillar grooves, and may detect water flow produced by currents, prey, predators, or conspecifics. Ventral non-pored canals and vesicles of Savi, which are found in benthic batoids, likely function as tactile or vibration receptors that encode displacements of the skin surface caused by prey, the substrate, or conspecifics. This mechanotactile mechanism is supported by the presence of compliant canal walls, neuromasts that are enclosed in wide diameter canals, and the presence of hair cells in neuromasts that are polarized both parallel to and nearly perpendicular to the canal axis in D. sabina. The mechanotactile, schooling, and mechanosensory parallel processing hypotheses are proposed as future directions to address the relationships between morphology and physiology of the mechanosensory lateral line system and behavior in elasmobranch fishes.