First published online April 18, 2008
Journal of Experimental Biology 211, 1355-1361 (2008)
Published by The Company of Biologists 2008
doi: 10.1242/jeb.010165
Behavioral and neural responses of juvenile crayfish to moving shadows
William H. Liden1 and
Jens Herberholz1,2,*
1 Department of Psychology, University of Maryland, College Park, MD 20742,
USA
2 Neuroscience and Cognitive Science Program, University of Maryland, College
Park, MD 20742, USA

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Fig. 1. Experimental set-up and shadow velocities. (A) Top view of the experimental
tank. Water containing food odor flows into a tunnel on the right side and
exits on the left. Animals enter the tunnel from the start compartment and
approach the food odor release point. A pair of bath electrodes is attached to
the tunnel walls, 8 cm from the tunnel entrance. The bath is grounded with a
ground wire. Shadows always move from right to left over the tank. (B) Side
view of the set-up. Animals inside the tank are filmed with a camera
positioned above the tank. The camera is connected to a TV monitor. Bath
electrodes are connected to an amplifier and an oscilloscope. Signals are
recorded on a computer. The shadow is produced by swinging a plastic rectangle
through a light beam directed onto the tank. The tank wall facing the light
and shadow apparatus is covered. (C) Average shadow velocities and
accelerations derived from five repeated measurements with silicone
photodiodes placed between the right tunnel wall and the bath electrodes.
Velocities and accelerations for all three shadows (slow, medium, fast) are
highly consistent as evidenced by small standard deviations.
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Fig. 2. Example of a tail-flip response and response patterns for different
shadows. (A) An example of a tail-flip response of a crayfish exposed to a
slow shadow. Shown are (1) the animal in the start compartment shortly after
the experiment was started, (2) the animal in the tunnel walking towards the
food odor release point and approaching the bath electrodes, (3) the animal
producing a tail-flip in response to the shadow and (4) the animal in its
final position after completing the tail-flip. (B) Patterns of behavior in
response to shadows of different velocities. The number of tail-flips
decreases with increasing shadow velocity while the number of stops increases.
The differences in response pattern are statistically significant
(*P 0.01).
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Fig. 3. Electric field potentials recorded with bath electrodes during tail-flips.
(A) An example trace of a tail-flip in response to a slow shadow. The action
potential of the medial giant neuron (MG, asterisks; magnified in the inset)
can be seen and enables non-ambiguous identification of the tail-flip as
mediated by giant neuron activity. The large deflections that follow are field
potentials generated by simultaneous muscle contractions caused by the giant
spike. (B) A second example trace of a tail-flip in response to a slow shadow
that is followed 43 ms later by a second tail-flip. The action potential of
the MG neuron (asterisks; magnified in the inset) can be seen for the first
tail-flip while the much smaller and less phasic potential for the second
tail-flip is characteristic of field potentials caused by activity in the
non-giant (Non-G; black arrow) circuit. See text for further explanation.
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© The Company of Biologists Ltd 2008