A comprehensive understanding of the control of flexible fins is fundamental to engineering underwater vehicles that perform like fish, since it is the fins that produce forces which control the fish's motion. However, little is known about the fin's sensory system or about how fish use sensory information to modulate the fin and to control propulsive forces. As part of a research program that involves neuromechanical and behavioral studies of the sunfish pectoral fin, a biorobotic model of the pectoral fin and of the fin's sensorimotor system was developed and used to investigate relationships between sensory information, fin ray motions and propulsive forces. This robotic fin is able to generate the motions and forces of the biological fin during steady swimming and turn maneuvers, and is instrumented with a relatively small set of sensors that represent the biological lateral line and receptors hypothesized to exist intrinsic to the pectoral fin. Results support the idea that fin ray curvature, and the pressure in the flow along the wall that represents the fish body, capture time-varying characteristics of the magnitude and direction of the force created throughout a fin beat. However, none of the sensor modalities alone are sufficient to predict the propulsive force. Knowledge of the time-varying force vector with sufficient detail for the closed-loop control of fin ray motion will result from the integration of characteristics of many sensor modalities.
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http://dx.doi.org/10.1088/1748-3182/5/3/035003 | DOI Listing |
J Fish Biol
January 2025
Minderoo-UWA Deep-Sea Research Centre, School of Biological Sciences and Oceans Institute, The University of Western Australia, Perth, Western Australia, Australia.
The deep-sea demersal fish fauna is characterized by a prevalence of elongated-body forms with long tapering tails. Using baited camera landers at depths of 4500-6300 m in the Pacific Ocean, we observed multiple instances of backward swimming using reverse undulation of the slender body in four species: the cutthroat eel Ilyophis robinsae, abyssal grenadier Coryphaenoides yaquinae, and cusk-eels Bassozetus sp. and Barathrites iris.
View Article and Find Full Text PDFJ Fish Biol
January 2025
Key Laboratory of Aquatic Ecology and Aquaculture of Tianjin, College of Fisheries, Tianjin Agricultural University, Tianjin, People's Republic of China.
Understanding the developmental sequence characteristics of the vertebral and appendicular skeletons of the larvae and juveniles of Larimichthys crocea (Naozhou population) can provide theoretical basis for seedling cultivation, environmental adaptation, and taxonomic identification. The cartilage-bone double staining method was used to stain, observe, and analyse the vertebrae, pectoral fins, anal fins, caudal fins, and dorsal fins of the larvae and juveniles of L. crocea (0-30 days post-hatching [DPH]).
View Article and Find Full Text PDFJ Fish Biol
January 2025
Department of Medicine and Technological Innovation, University of Insubria, Varese, Italy.
Background: Batoids possess a unique body plan associated with a benthic lifestyle that includes dorsoventral compression and anteriorly expanded pectoral fins that fuse to the rostrum. The family Myliobatidae, including manta rays and their relatives, exhibit further modifications associated with invasion of the pelagic environment, and the evolution of underwater flight. Notably, the pectoral fins are split into two domains with independent functions that are optimized for feeding and oscillatory locomotion.
View Article and Find Full Text PDFZookeys
December 2024
Center for Advanced Technical and Educational Supports, Faculty of Agriculture, Kyushu University, Fukuoka 819-0395, Japan.
A unique species of the flappy-snake eel genus, , is described based on a single specimen (270 mm in total length) collected from Dong-gang, southwestern Taiwan. The new species possesses several characters that are distinct from the only other species in the genus, . can be easily distinguished from by having two papillae inside of nasal tube (vs three in ), 25 branchiostegal rays (vs 29), the dorsal-fin origin positioned behind the tip of the pectoral fin (vs not behind, usually above mid-pectoral fin), and the absence of the maxillary teeth (vs present).
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