scholarly journals The valvula cerebelli of the spiny eel, Macrognathus aculeatus, receives primary lateral-line afferents from the rostrum of the upper jaw

1991 ◽  
Vol 266 (2) ◽  
pp. 285-293 ◽  
Author(s):  
Mario F. Wullimann ◽  
Michael H. Hofmann ◽  
Dietrich L. Meyer
1981 ◽  
Vol 36 (5-6) ◽  
pp. 493-496 ◽  
Author(s):  
Bernd Fritzsch

Abstract The arrangement of the lateral line afferents of salamanders as revealed by transganglionic staining with horse­ radish peroxidase is described. Each lateral line organ is supplied by two fibers only. In the medulla these two afferent fibers run in separate fiber bundles. It is suggested, that only those fibers contacting lateral line sensory cells with the same polarity form together one bundle. Bundles formed by anterior or posterior lateral line afferents are also clearly separated. Beside the lateral line organs smaller pit organs are described. These organs are supplied by one afferent only which reveals an arrangement in the medulla different from that of the lateral line afferents. Based on anatomical facts, these small pit organs are considered to be electroreceptors. Centrifugally projecting neurons, most probably efferents, are described in the medulla.


1984 ◽  
Vol 229 (3) ◽  
pp. 451-469 ◽  
Author(s):  
Bernd Fritzsch ◽  
Alfeo M. Nikundiwe ◽  
Udo Will

Zootaxa ◽  
2020 ◽  
Vol 4772 (3) ◽  
pp. 545-566 ◽  
Author(s):  
SATOSHI MORISHITA ◽  
HIROYUKI MOTOMURA

A new barracuda, Sphyraena stellata, is described on the basis of 41 specimens [98.0–587.0 mm standard length (SL)] collected from the Indo-Pacific. The new species can be distinguished from all congeners in having the following combination of characters: one gill raker on first gill arch; pelvic-fin insertion located slightly before vertical through first dorsal-fin origin; pored lateral-line scales 134–141 (modally 137), total lateral-line scales 139–148 (146); scales above and below lateral line 15–17 (15) and 14–16 (15), respectively; snout comparatively short, its length 13.6–15.8 (mean 14.4) % SL; upper jaw short, its posterior tip not reaching to below anterior nostril, its length 10.0–12.2 (10.8) % SL; eye small, orbit diameter and depth 4.3–7.0 (4.9) and 3.9–5.6 (4.5) % SL, respectively; anal-fin base shortish, its length 6.9–8.1 (7.5) % SL; last dorsal- and anal-fin ray lengths 4.0–5.6 (4.7) and 3.6–5.6 (4.6) % SL, respectively; anus not close to anal-fin origin, anterior and posterior margins of former to anal-fin origin 7.5–11.9 (9.9) and 5.2–8.3 (6.8) % of head length, respectively; head sensory canal pores on suborbital area simple or slightly branched, their lowermost parts not close to margin of lacrimal bone, large smooth area lacking canal pores on mid-margin of lacrimal bone; two yellow stripes on lateral surface of body (remaining as black stripes in preserved specimens); and caudal fin gray. In addition, S. helleri Jenkins, 1901 and S. novaehollandiae Günther, 1860, both being closely related to the new species, are redescribed on the basis of 4 (243.3–545.8 mm SL) and 15 (270.8–598.0 mm SL) specimens, including holotypes, respectively, with new diagnostic characters proposed for both species. 


2000 ◽  
Vol 203 (16) ◽  
pp. 2495-2502 ◽  
Author(s):  
R. Voigt ◽  
A.G. Carton ◽  
J.C. Montgomery

The mechanoreceptive lateral line system detects hydrodynamic stimuli and plays an important role in a number of types of fish behaviour, including orientation to water currents. The lateral line is composed of hair cell receptor organs called neuromasts that occur as superficial neuromasts on the surface of the skin or canal neuromasts located in subepidermal canals. Both are innervated by primary afferents of the lateral line nerves. Although there have been extensive studies of the response properties of lateral line afferents to vibrating sources, their response to water flow has not been reported. In this study, we recorded extracellularly from anterior lateral line afferents in the New Zealand long-fin eel Anguilla dieffenbachii while stimulating the eel with unidirectional water flows at 0.5-4 cm s(−)(1). Of the afferents, 80 % were flow-sensitive to varying degrees, the response magnitude increasing with flow rate. Flow-sensitive fibres gave non-adapting tonic responses, indicating that these fibres detect absolute flow velocity. Further studies are needed to confirm whether flow-sensitive and flow-insensitive fibres correlate with superficial and canal neuromasts, respectively.


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