spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Coombs, S.
Right arrow Articles by Donovan, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Coombs, S.
Right arrow Articles by Donovan, B.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Journal of Experimental Biology, Vol 204, Issue 2 337-348, Copyright © 2001 by Company of Biologists


JOURNAL ARTICLES

The orienting response of Lake Michigan mottled sculpin is mediated by canal neuromasts

S Coombs, CB Braun and B Donovan
Parmly Hearing Institute, Loyola University of Chicago, Chicago, IL 60626, USA. scoombs@luc.edu

Lake Michigan mottled sculpin, Cottus bairdi, exhibit a naturally occurring and unconditioned orienting response that can be triggered by both live prey and chemically inert vibrating spheres, even in blinded animals. CoCl(2)-induced reductions of the orienting response demonstrate that the lateral line is required for this behavior in the absence of non-mechanosensory cues (such as vision), but shed no light on the relative contributions of superficial and canal neuromasts to this behavior. To determine the relative roles of these two subsystems, we measured the frequency with which mottled sculpin oriented towards a small vibrating sphere before and after two treatments: (i) immersion of fish in a solution of gentamicin, an aminoglycoside antibiotic that damages hair cells in canal, but not superficial, neuromasts; and (ii) scraping the skin of the fish, which damages the superficial, but not the canal, neuromasts. To ensure that both superficial and canal neuromasts were adequately stimulated, we tested at different vibration frequencies (10 and 50 Hz) near or at the best frequency for each type of neuromast. At both test frequencies, response rates before treatment were greater than 70 % and were significantly greater than 'spontaneous' response frequencies measured in the absence of sphere vibration. Response rates fell to spontaneous levels after 1 day of gentamicin treatment and did not return to pre-treatment levels for 10-15 days. In contrast, response rates stayed approximately the same after superficial neuromasts had been damaged by skin abrasion. Scanning electron microscopy confirmed hair cell damage (loss of apical cilia) in canal, but not superficial, neuromasts of gentamicin-treated animals after as little as 24 h of treatment. The sensory epithelium of canal neuromasts gradually returned to normal, following a time course similar to behavioral loss and recovery of the orienting response, whereas that of superficial neuromasts appeared normal throughout the entire period. This study shows that the orienting response of the mottled sculpin is mediated by canal neuromasts.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
M. A. Rapo, H. Jiang, M. A. Grosenbaugh, and S. Coombs
Using computational fluid dynamics to calculate the stimulus to the lateral line of a fish in still water
J. Exp. Biol., May 15, 2009; 212(10): 1494 - 1505.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
S. R. Pluta and M. Kawasaki
Multisensory enhancement of electromotor responses to a single moving object
J. Exp. Biol., September 15, 2008; 211(18): 2919 - 2930.
[Abstract] [Full Text] [PDF]


Home page
Phil Trans R Soc BHome page
J. C Liao
A review of fish swimming mechanics and behaviour in altered flows
Phil Trans R Soc B, November 29, 2007; 362(1487): 1973 - 1993.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
J. M. Gardiner and J. Atema
Sharks need the lateral line to locate odor sources: rheotaxis and eddy chemotaxis
J. Exp. Biol., June 1, 2007; 210(11): 1925 - 1934.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
J. C. Liao
The role of the lateral line and vision on body kinematics and hydrodynamic preference of rainbow trout in turbulent flow
J. Exp. Biol., October 15, 2006; 209(20): 4077 - 4090.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
L. M. Palmer, M. Deffenbaugh, and A. F. Mensinger
Sensitivity of the anterior lateral line to natural stimuli in the oyster toadfish, Opsanus tau (Linnaeus)
J. Exp. Biol., September 15, 2005; 208(18): 3441 - 3450.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
D. T. T. Plachta, W. Hanke, and H. Bleckmann
A hydrodynamic topographic map in the midbrain of goldfish Carassius auratus
J. Exp. Biol., October 1, 2003; 206(19): 3479 - 3486.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
M. J. Kanter and S. Coombs
Rheotaxis and prey detection in uniform currents by Lake Michigan mottled sculpin (Cottus bairdi)
J. Exp. Biol., January 1, 2003; 206(1): 59 - 70.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
S. Krother, J. Mogdans, and H. Bleckmann
Brainstem lateral line responses to sinusoidal wave stimuli in still and running water
J. Exp. Biol., May 15, 2002; 205(10): 1471 - 1484.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2001