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Keywords: lateral line
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Journal Articles
In collection:
Neuroethology
J Exp Biol (2020) 223 (23): jeb223008.
Published: 7 December 2020
... sources of current-borne odors, to intercept invertebrate drift and, in general, to conserve energy while preventing downstream displacement. Sensory information available for rheotaxis includes water-motion cues to the lateral line and body-motion cues to visual, vestibular or tactile senses when fish...
Includes: Supplementary data
Journal Articles
In collection:
Neuroethology
J Exp Biol (2016) 219 (18): 2781–2789.
Published: 15 September 2016
...Julie M. Butler; Karen P. Maruska ABSTRACT Signals produced during social interactions convey crucial information about the sender's identity, quality, reproductive state and social status. Fishes can detect near-body water movements via the mechanosensory lateral line system, and this sense...
Journal Articles
In collection:
Neuroethology
J Exp Biol (2016) 219 (18): 2823–2827.
Published: 15 September 2016
...) and the mottled sculpin (cottus bairdi) . J. Exp. Biol.   190 , 109 - 129 . Coombs , S. and Janssen , J. ( 1990 ). Behavioral and neurophysiological assessment of lateral line sensitivity in the mottled sculpin, Cottus bairdi . J. Comp. Physiol. A   167 , 557 - 567 . 10.1007/BF00190827...
Includes: Supplementary data
Journal Articles
J Exp Biol (2016) 219 (4): 582–589.
Published: 15 February 2016
... an example of learning in a model system that offers promise for understanding its neurophysiological basis. We tested the role of the LLS in the foraging of zebrafish by comparing rates of prey strikes and captures between fish with a compromised lateral line system and control fish. These experiments...
Journal Articles
J Exp Biol (2015) 218 (18): 2826–2829.
Published: 1 September 2015
...Gary E. Baker; Willem J. de Grip; Michael Turton; Hans-Joachim Wagner; Russell G. Foster; Ron H. Douglas ABSTRACT Using immunohistochemistry and western blot analysis, we demonstrate that melanopsin is localised in cells around the central pore of lateral line neuromasts in the African clawed frog...
Journal Articles
J Exp Biol (2015) 218 (10): 1603–1612.
Published: 15 May 2015
...Matthew Kulpa; Joseph Bak-Coleman; Sheryl Coombs ABSTRACT When encountering a unidirectional flow, many fish exhibit an unconditioned orienting response known as rheotaxis. This multisensory behavior can reportedly involve visual, vestibular, tactile and lateral line cues. However, the precise...
Journal Articles
J Exp Biol (2015) 218 (9): 1373–1385.
Published: 1 May 2015
... new phenomena. Particle image velocimetry Boundary layer Lateral line Oncorhynchus mykiss Skin friction Swimming performance Skin friction is a major source of resistance to a swimming fish ( Webb, 1975 ). The possibility that compression of the boundary layer due to undulatory...
Journal Articles
J Exp Biol (2014) 217 (24): 4328–4336.
Published: 15 December 2014
... in front of the predator using the lateral line system. This flow, known as the bow wave, was visualized and modeled with computational fluid dynamics. According to the predictions of the model, larvae direct their escape away from the side of their body exposed to more rapid flow. This suggests that prey...
Includes: Supplementary data
Journal Articles
J Exp Biol (2014) 217 (24): 4347–4355.
Published: 15 December 2014
... and central role in many marine ecosystems. Bioacoustics Cephalopod Hearing Noise Loudness Invertebrate Ear Statocyst Lateral line All animals showed clear behavioral responses to acoustic stimuli (Figs 1 , 2 ), and the intensity of the response was associated with the amplitude...
Includes: Supplementary data
Journal Articles
J Exp Biol (2014) 217 (13): 2338–2347.
Published: 1 July 2014
... non-visual sensory systems, in particular the flow-sensing lateral line, is poorly understood, largely because of widely varying methods and sensory conditions for studying rheotaxis. Here, we examine how sedentary behavior under visually deprived conditions affects the relative importance of lateral...
Includes: Supplementary data
Journal Articles
J Exp Biol (2014) 217 (12): 2078–2088.
Published: 15 June 2014
...Allison B. Coffin; David G. Zeddies; Richard R. Fay; Andrew D. Brown; Peter W. Alderks; Ashwin A. Bhandiwad; Robert A. Mohr; Michael D. Gray; Peter H. Rogers; Joseph A. Sisneros We investigated the roles of the swim bladder and the lateral line system in sound localization behavior by the plainfin...
Includes: Supplementary data
Journal Articles
J Exp Biol (2014) 217 (9): 1570–1579.
Published: 1 May 2014
... are potentially stimulated by the particle motion component of sound. The encoding of the anterior lateral line nerve to acoustic stimuli in freely behaving oyster toadfish, Opsanus tau , was examined. Nerve sensitivity and directional responses were determined using spike rate and vector strength analysis...
Journal Articles
J Exp Biol (2013) 216 (21): 4011–4024.
Published: 1 November 2013
... sensory conditions on the spatiotemporal dynamics of rheotaxis. Although the overall ability of giant danio ( Devario aequipinnatus ) to head upstream is largely unaffected by either unimodal or bimodal deprivation of visual and/or lateral line senses, the spatiotemporal form of the behavior is altered...
Journal Articles
J Exp Biol (2013) 216 (18): 3504–3513.
Published: 15 September 2013
... of −19 to −10 dB re. 1 m s −2 , respectively. Hearing thresholds of prepulse tones were considerably lower than previously predicted by startle response assays. The PPI assay was also used to investigate the relative contribution of the lateral line to the detection of acoustic stimuli. After...
Journal Articles
J Exp Biol (2013) 216 (18): 3522–3530.
Published: 15 September 2013
...Julia A. Sampson; Jim Duston; Roger P. Croll SUMMARY To investigate whether mechanoreception is used in non-visual feeding in larval striped bass ( Morone saxatilis ), the ontogeny of superficial neuromasts along the lateral line was described using the vital stain FM1-43FX and fluorescent...
Journal Articles
J Exp Biol (2013) 216 (16): 3084–3089.
Published: 15 August 2013
... in the dark to remove visual input and/or temporarily blocking lateral line input via immersion in cobalt chloride. Fish used their pectoral fins to touch obstacles as they swam slowly past them under all conditions. Loss of visual and/or lateral line sensory input resulted in an increased number of fin taps...
Includes: Supplementary data
Journal Articles
J Exp Biol (2013) 216 (13): 2515–2522.
Published: 1 July 2013
... published work, that these are derived embryonically from lateral line placodes. Finally, we review hypotheses to explain the distribution of electroreception within teleosts, including the hypothesis that teleost ampullary and tuberous electroreceptors evolved via the modification of mechanosensory hair...
Journal Articles
J Exp Biol (2012) 215 (22): 3944–3954.
Published: 15 November 2012
... by its relative high standard metabolic rate and optimal (i.e. least cost) swimming speed. To test the hypothesis that lateral line afferent information contributes to efficient locomotion in an active pelagic species, the swimming performance of S. lalandi was evaluated after unilateral disruption...
Journal Articles
J Exp Biol (2012) 215 (12): 2060–2071.
Published: 15 June 2012
...Margot A. B. Schwalbe; Daniel K. Bassett; Jacqueline F. Webb SUMMARY The cranial lateral line canal system of teleost fishes is morphologically diverse and is characterized by four patterns. One of these, widened lateral line canals, has evolved convergently in a wide range of teleosts, including...
Journal Articles
J Exp Biol (2011) 214 (20): 3358–3367.
Published: 15 October 2011
...Mana Mirjany; Thomas Preuss; Donald S. Faber SUMMARY Goldfish ( Carassius auratus ) escape responses to sudden auditory stimuli are mediated by a pair of reticulospinal neurons, the Mauthner (M-) cells, which integrate mechanosensory inputs from the inner ear and the lateral line (LL) to initiate...