Shark depredation: future directions in research and management.

Shark depredation is a complex social-ecological issue that affects a range of fisheries worldwide. Increasing concern about the impacts of shark depredation, and how it intersects with the broader context of fisheries management, has driven recent research in this area, especially in Australia and the United States. This review synthesises these recent advances and provides strategic guidance for researchers aiming to characterise the occurrence of depredation, identify the shark species responsible, and test deterrent and management approaches to reduce its impacts. Specifically, the review covers the application of social science approaches, as well as advances in video camera and genetic methods for identifying depredating species. The practicalities and considerations for testing magnetic, electrical, and acoustic deterrent devices are discussed in light of recent research. Key concepts for the management of shark depredation are reviewed, with recommendations made to guide future research and policy development. Specific management responses to address shark depredation are lacking, and this review emphasizes that a "silver bullet" approach for mitigating depredation does not yet exist. Rather, future efforts to manage shark depredation must rely on a diverse range of integrated approaches involving those in the fishery (fishers, scientists and fishery managers), social scientists, educators, and other stakeholders.

Electrosensory Impairment in the Atlantic Stingray, Hypanus sabinus, After Crude Oil Exposure.

Elasmobranchs are renowned for their extremely sensitive electrosensory system, which is used to detect predators, prey, and mates, and is possibly used for navigation. The proper functioning of the electrosensory system is thus critical to fitness. The objective of this study was to test whether exposure to crude oil impairs the electroreceptive capabilities of elasmobranch fishes. Electrosensory function was quantified from six stingrays before and after exposure to a concentration of oil that mimicked empirically measured concentrations along the coast of Louisiana following the Deepwater Horizon spill. Orientation distance (cm), and angle with respect to the dipole axis of a prey-simulating electric field were used to derive the electric field intensity that elicited a response. Oil exposed stingrays continued to exhibit feeding behavior, but they initiated orientations to prey-simulating electric fields from a significantly closer orientation distance. The mean orientation distance after oil exposure was 5.29 ± 0.41 SE cm compared to a pre-exposure orientation distance of 7.16 ± 0.66 SE cm. Stingrays required a mean electric field intensity of 0.596 ± 0.21 SE µV cm-1 to initiate a response after oil exposure, compared to a mean of only 0.127 ± 0.03 SE µV cm-1 in uncontaminated seawater. Oil exposed stingrays thus exhibited a response to a stimulus approximately 4.7 times greater than controls. Stingrays impacted by an oil spill appear to experience reduced electrosensory capabilities, which could detrimentally impact fitness. This study is the first to quantify the effects of crude oil on behavioral electrosensory function.

Sensory systems in sawfishes. 1. The ampullae of Lorenzini.

The distribution and density of the ampullary electroreceptors in the skin of elasmobranchs are influenced by the phylogeny and ecology of a species. Sensory maps were created for 4 species of pristid sawfish. Their ampullary pores were separated into pore fields based on their innervation and cluster formation. Ventrally, ampullary pores are located in 6 areas (5 in Pristis microdon), covering the rostrum and head to the gills. Dorsally, pores are located in 4 areas (3 in P. microdon), which cover the rostrum, head and may extend slightly onto the pectoral fins. In all species, the highest number of pores is found on the dorsal and ventral sides of the rostrum. The high densities of pores along the rostrum combined with the low densities around the mouth could indicate that sawfish use their rostrum to stun their prey before ingesting it, but this hypothesis remains to be tested. The directions of ampullary canals on the ventral side of the rostrum are species specific. P. microdon possesses the highest number of ampullary pores, which indicates that amongst the study species this species is an electroreception specialist. As such, juvenile P. microdon inhabit low-visibility freshwater habitats.

Enhanced visual fields in hammerhead sharks.

Several factors that influence the evolution of the unusual head morphology of hammerhead sharks (family Sphyrnidae) are proposed but few are empirically tested. In this study we tested the 'enhanced binocular field' hypothesis (that proposes enhanced frontal binocularity) by comparison of the visual fields of three hammerhead species: the bonnethead shark, Sphyrna tiburo, the scalloped hammerhead shark, Sphyrna lewini, and the winghead shark, Eusphyra blochii, with that of two carcharhinid species: the lemon shark, Negaprion brevirostris, and the blacknose shark, Carcharhinus acronotus. Additionally, eye rotation and head yaw were quantified to determine if species compensate for large blind areas anterior to the head. The winghead shark possessed the largest anterior binocular overlap (48 deg.) and was nearly four times larger than that of the lemon (10 deg.) and blacknose (11 deg.) sharks. The binocular overlap in the scalloped hammerhead sharks (34 deg.) was greater than the bonnethead sharks (13 deg.) and carcharhinid species; however, the bonnethead shark did not differ from the carcharhinids. These results indicate that binocular overlap has increased with lateral head expansion in hammerhead sharks. The hammerhead species did not demonstrate greater eye rotation in the anterior or posterior direction. However, both the scalloped hammerhead and bonnethead sharks exhibited greater head yaw during swimming (16.9 deg. and 15.6 deg., respectively) than the lemon (15.1 deg.) and blacknose (15.0 deg.) sharks, indicating a behavioral compensation for the anterior blind area. This study illustrates the larger binocular overlap in hammerhead species relative to their carcharhinid sister taxa and is consistent with the 'enhanced binocular field' hypothesis.

Electroreception in the euryhaline stingray, Dasyatis sabina.

This study quantified the electrosensitivity of a euryhaline elasmobranch, the Atlantic stingray (Dasyatis sabina) across a range of salinities. Specimens from a permanent freshwater (FW) population in the St Johns River system, FL, USA, were compared with stingrays from the tidally dynamic Indian River Lagoon in east Florida, USA. Behavioral responses of stingrays to prey-simulating electric stimuli were quantified in FW (0 p.p.t., rho=2026 Omega cm), brackish (15 p.p.t., rho=41 Omega cm) and full strength seawater (35 p.p.t., rho=19 Omega cm). This study demonstrated that the electrosensitivity of D. sabina is significantly reduced in FW. In order to elicit a feeding response, stingrays tested in FW required an electric field 200-300x greater than stingrays tested in brackish and saltwater (median FW treatments=1.4 microV cm(-1), median brackish-saltwater treatments=6 nV cm(-1)), and the maximum orientation distance was reduced by 35.2%, from 44.0 cm in the brackish and saltwater treatments to 28.5 cm in FW. The St Johns River stingrays did not demonstrate an enhanced electrosensitivity in FW, nor did they exhibit reduced sensitivity when introduced to higher salinities. Stingrays from both populations responded similarly to the prey-simulating stimulus when tested at similar salinities, regardless of their native environment. The reduction in electrosensitivity and detection range in FW is attributed to both an environmental factor (electrical resistivity of the water) and the physiological function of the ampullary canals. The plasticity of this sensory system to function across such a wide environmental range demonstrates its adaptive significance.