JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 84: 2181-2190, 2000;
0022-3077/00 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (18)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Earhart, G. M.
Right arrow Articles by Stein, P. S. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Earhart, G. M.
Right arrow Articles by Stein, P. S. G.

The Journal of Neurophysiology Vol. 84 No. 5 November 2000, pp. 2181-2190
Copyright ©2000 by the American Physiological Society

Step, Swim, and Scratch Motor Patterns in the Turtle

Gammon M. Earhart and Paul S. G. Stein

Department of Biology and Program in Movement Science, Washington University, St. Louis, Missouri 63130

Earhart, Gammon M. and Paul S. G. Stein. Step, Swim, and Scratch Motor Patterns in the Turtle. J. Neurophysiol. 84: 2181-2190, 2000. The turtle generates a variety of coordinated hindlimb movements, including different forms of locomotion and scratching. The intact turtle produces forward step, forward swim, and backpaddle. Following spinal cord transection, rostral, pocket, and caudal scratches can be evoked by mechanical stimulation of the shell. Comparisons of the kinematics and motor patterns of these six behaviors provide insights regarding neuronal mechanisms underlying their production. All six behaviors were characterized by alternating hip flexion and extension and by an event during which force was exerted against a substrate. The portion of the cycle occupied by hip flexion or extension movement varied across behaviors. Hip extension occupied well over half the cycle period in the forward step and the caudal scratch. The cycle was split into approximately half hip flexion and half hip extension for the forward swim, the backpaddle, and the rostral scratch. Hip flexion occupied over half the cycle in the pocket scratch. The swim and scratch forms had curvilinear, crescent-shaped toe trajectories and a single burst of monoarticular knee extensor activity during each cycle. The forward step had a linear toe trajectory and two bursts of knee extensor activity during each cycle, one during swing and one during stance. Timing of monoarticular knee extensor onset was similar for: the forward swim, the rostral scratch, and the swing phase burst of forward step; the pocket scratch and the stance phase burst of forward step; and the backpaddle and the caudal scratch. Amplitudes of muscle activity varied among the six behaviors; high amplitudes of activity were associated with events during which force was exerted against a substrate. These times of force exertion were: stance phase in the forward step, powerstroke in the forward swim and the backpaddle, and rubs of the limb against the shell in the scratch forms. The six behaviors studied represent a range of parameter values, as evidenced by relative durations of hip flexion to hip extension, knee extensor phasing, and electromyogram (EMG) amplitudes. This range of behaviors could be produced by assembling different combinations of neurons from a common pool, with all six behaviors likely sharing some basic circuitry. The extent of shared circuitry may be greater between behaviors with similar timing, e.g., backpaddle and caudal scratch.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
A. Berkowitz
Physiology and Morphology of Shared and Specialized Spinal Interneurons for Locomotion and Scratching
J Neurophysiol, June 1, 2008; 99(6): 2887 - 2901.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. F. Samara and S. N. Currie
Location of Spinal Cord Pathways That Control Hindlimb Movement Amplitude and Interlimb Coordination During Voluntary Swimming in Turtles
J Neurophysiol, April 1, 2008; 99(4): 1953 - 1968.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. F. Samara and S. N. Currie
Crossed Commissural Pathways in the Spinal Hindlimb Enlargement Are Not Necessary for Right Left Hindlimb Alternation During Turtle Swimming
J Neurophysiol, October 1, 2007; 98(4): 2223 - 2231.
[Abstract] [Full Text] [PDF]


Home page
Integr. Comp. Biol.Home page
A. Prochazka and S. Yakovenko
Predictive and reactive tuning of the locomotor CPG
Integr. Comp. Biol., October 1, 2007; 47(4): 474 - 481.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. Ausborn, W. Stein, and H. Wolf
Frequency Control of Motor Patterning by Negative Sensory Feedback
J. Neurosci., August 29, 2007; 27(35): 9319 - 9328.
[Abstract] [Full Text] [PDF]


Home page
Integr. Comp. Biol.Home page
K. Nishikawa, A. A. Biewener, P. Aerts, A. N. Ahn, H. J. Chiel, M. A. Daley, T. L. Daniel, R. J. Full, M. E. Hale, T. L. Hedrick, et al.
Neuromechanics: an integrative approach for understanding motor control
Integr. Comp. Biol., July 1, 2007; 47(1): 16 - 54.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
K. E. Musselman and J. F. Yang
Loading the Limb During Rhythmic Leg Movements Lengthens the Duration of Both Flexion and Extension in Human Infants
J Neurophysiol, February 1, 2007; 97(2): 1247 - 1257.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
D. M. Neustadter, R. L. Herman, R. F. Drushel, D. W. Chestek, and H. J. Chiel
The kinematics of multifunctionality: comparisons of biting and swallowing in Aplysia californica
J. Exp. Biol., January 15, 2007; 210(2): 238 - 260.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
G. Rivera, A. R. V. Rivera, E. E. Dougherty, and R. W. Blob
Aquatic turning performance of painted turtles (Chrysemys picta) and functional consequences of a rigid body design
J. Exp. Biol., November 1, 2006; 209(21): 4203 - 4213.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Berkowitz
Physiology and Morphology Indicate That Individual Spinal Interneurons Contribute to Diverse Limb Movements
J Neurophysiol, December 1, 2005; 94(6): 4455 - 4470.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. Cangiano and S. Grillner
Mechanisms of Rhythm Generation in a Spinal Locomotor Network Deprived of Crossed Connections: The Lamprey Hemicord
J. Neurosci., January 26, 2005; 25(4): 923 - 935.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
P. S.G. Stein and S. Daniels-McQueen
Timing of Knee-Related Spinal Neurons During Fictive Rostral Scratching in the Turtle
J Neurophysiol, December 1, 2003; 90(6): 3585 - 3593.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
P. S. G. Stein and S. Daniels-McQueen
Modular Organization of Turtle Spinal Interneurons during Normal and Deletion Fictive Rostral Scratching
J. Neurosci., August 1, 2002; 22(15): 6800 - 6809.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
G. B. Gillis and A. A. Biewener
Hindlimb muscle function in relation to speed and gait: in vivo patterns of strain and activation in a hip and knee extensor of the rat (Rattus norvegicus)
J. Exp. Biol., January 8, 2001; 204(15): 2717 - 2731.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online