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 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 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 Google Scholar
Google Scholar
Right arrow Articles by FRASER, P. J.
Right arrow Articles by CLARAC, F.
Right arrow Search for Related Content
PubMed
Right arrow Articles by FRASER, P. J.
Right arrow Articles by CLARAC, F.
Journal of Experimental Biology 130,305-330 (1987)
Published by Company of Biologists 1987


Swimming Patterns and the Activity of Identified Equilibrium Interneurones in the Shore Crab, Carcinus Maenas

P. J. FRASER 1, M. BÉVENGUT 2, and F. CLARAC 2

1 Laboratoire de Neurobiologie et Physiologie Comparées, Place Pevneau, 33120 Arcachon, France; Department of Zoology, Aberdeen University, Tillydrone Avenue, Aberdeen AB9 2TN, Scotland
2 Laboratoire de Neurobiologie et Physiologie Comparées, Place Pevneau, 33120 Arcachon, France

Swimming behaviour in crabs is electromyographically described in relation to the involvement of the discharge of the equilibrium interneurones. In intact crabs or crabs with only the fifth legs remaining, swimming consists of cyclic out-of-phase sculling movements of the last pair of pereïopods (P5). In these legs, all muscles are involved within a single swimming cycle; antagonistic muscles burst alternately, as do bilateral pairs of muscles. Bursting in the four proximal muscles ensures the appendage rotation while distal muscles set the scull in the best propulsive position.

Swimming evoked by tilt in the sagittal plane starts with symmetrical remotor activity before alternate bursting begins. Tilt in the plane of a statocyst vertical canal leads to asymmetrical onset of remotor bursting, starting with the muscle contralateral to the stimulated statocyst.

Tilt in defined vertical planes elicits the discharge of identified equilibrium interneurones. Of these, interneurones C and D are active before and during swimming. Sensory inputs from the statocysts and/or the leg proprioceptors to these interneurones are both adequate to drive swimming. Moreover, our experiments suggest that cell C activity is strongly involved in the onset and the maintenance of swimming behaviour.

Swimming can be altered by autotomy of legs on one side performed a few days in advance, and leads to the same turning tendency as does contralateral cutting of a connective. This may be due to modification in the strength of the remaining central connections to compensate for those lost.

Note:
To whom reprint requests should be addressed.

Key words: crab, swimming, electromyography, equilibrium interneurones, autotomy

Accepted on March 9, 1987







© The Company of Biologists Ltd 1987