|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Journal of Experimental Biology, Vol 199, Issue 11 2511-2529, Copyright © 1996 by Company of Biologists
JOURNAL ARTICLES |
KC Nishikawa and C Gans
Department of Biological Sciences, Northern Arizona University, Flagstaff 86011-5640, USA.
Electromyography, kinematic analysis, muscle stimulation and denervation techniques were used to investigate the muscular mechanisms of narial closure during breathing and of tongue protraction during prey capture in the marine toad Bufo marinus. Toads were video-taped during breathing and feeding under a variety of conditions: before surgery, after unilateral or bilateral denervation of the M. submentalis, and after unilateral or bilateral denervation of the Mm. genioglossus basalis and medialis. Deeply anesthetized toads were video-taped during stimulation of several cranial muscles, and electromyograms were recorded from the M. submentalis during feeding before and after its denervation. Bufo marinus differs from many other anurans in having a relatively long tongue that experiences large accelerations (> 31 g) during protraction. Tongue protraction occurs in two phases: an early phase during which the lingual tip moves upward and forward relative to the mandibular tip as the tongue shortens, and a later phase during which the lingual tip moves downward and forward relative to the mandibular tip as the tongue elongates under its own momentum. Relative to an external reference, the lingual tip follows a straight trajectory from mouth to prey, which depends critically upon precise coordination of tongue and jaw movements. The M. submentalis is necessary for normal tongue protraction during feeding. In contrast, the Mm. genioglossus basalis and medialis are necessary for forward movement of the tongue pad over the symphysis. In B. marinus, a simple anatomical change (elongation of the tongue) has functional consequences (inertial elongation) that profoundly affect the mechanisms of neuromuscular control. Though seldom studied, it seems likely that morphological evolution has had a profound influence on mechanisms of motor control in animals generally.
This article has been cited by other articles:
![]() |
A. K. Lappin, J. A. Monroy, J. Q. Pilarski, E. D. Zepnewski, D. J. Pierotti, and K. C. Nishikawa Storage and recovery of elastic potential energy powers ballistic prey capture in toads J. Exp. Biol., July 1, 2006; 209(13): 2535 - 2553. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. J. Meyers, J. C. O'Reilly, J. A. Monroy, and K. C. Nishikawa Mechanism of tongue protraction in microhylid frogs J. Exp. Biol., January 1, 2004; 207(1): 21 - 31. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. S. Hedrick and R. E. Winmill Excitatory and inhibitory effects of tricaine (MS-222) on fictive breathing in isolated bullfrog brain stem Am J Physiol Regulatory Integrative Comp Physiol, February 1, 2003; 284(2): R405 - R412. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. M. Deban, J. C. O'Reilly, and K. C. Nishikawa The Evolution of the Motor Control of Feeding in Amphibians Integr. Comp. Biol., December 1, 2001; 41(6): 1280 - 1298. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. S. Mallett, G. T. Yamaguchi, J. M. Birch, and K. C. Nishikawa Feeding Motor Patterns in Anurans: Insights from Biomechanical Modeling Integr. Comp. Biol., December 1, 2001; 41(6): 1364 - 1374. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Deban and U Dicke Motor control of tongue movement during prey capture in plethodontid salamanders J. Exp. Biol., January 12, 1999; 202(24): 3699 - 3714. [Abstract] [PDF] |
||||
![]() |
K. Nishikawa, W. Kier, and K. Smith Morphology and mechanics of tongue movement in the African pig-nosed frog Hemisus marmoratum: a muscular hydrostatic model J. Exp. Biol., January 4, 1999; 202(7): 771 - 780. [Abstract] [PDF] |
||||