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Behavioral components of prey capture in the frog
1 2 3 4 2,3 none of the behavioral components are a necessary prerequisite for the others to occur: they are independent “FAPs” If these are FAPs in the true sense the lets find what controls its: Step 1 Find cell/s that recognize prey
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Laboratory analysis of innate orientation behavior of toad to varying stimuli
Toad in glass jar above turntable Turntable used to pass targets in front of toad Results: Toad optimally responds to “worm-like” stimuli Worm must move along long axis but can move in any direction Orientation responses to worm are consistent FAPs “they are invariant.”
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Sensory transduction: the eye
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Sensory transduction: the retina
Rods and cones (toads rods only) Bipolar cells Amacrine cells Horizontal cells Ganglion cell Optic nerve (blind spot)
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Sensory transduction: the retina
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Synaptic interactions of bipolar, horizontal and amacrine cells produce center surround fields in ganglion cells Results from intracellular recordings
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Vertebrate ganglion cells in general can be classified into two types
On-center/off-surround Off-center/on-surround Additionally, some are sensitive to movement in their field
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The retina is a matrix of overlapping center/surround fields of ganglion cells
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The search for the cell/s that recognize prey features
Neurophysiological method: Animal placed on stage Electrodes placed in specific neuropil Stimulated visually while recording from cells Results 1: Retinal ganglion cells can be typed based on response type based on size of receptive field: R2 4 degrees R3 8 degrees R4 16 degrees -no ganglion cell matched behavior
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Visual pathway in the toad
Optic nerve crosses at the optic chiasm and projects contralaterally to: Optic tectum Pre-tectum of the thalamus Retinotopic organization is maintained in both these regions
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Example of Retinotopy from the Macaque visual system
A flickering stimulus Retinotopic representation in layer 4C of V1 Tootell et al (1988a).
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Retinotopic organization is maintained in both these regions
Cross sectional reference Thalamus
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The search for the cell that recognizes prey
Results 2: Thalamic pretectal TH3 cell responses to test stimuli Small receptive fields Responsive to moving stimuli Collectively (as a population) map visual field Do not correlate to behavior- are not prey detectors
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The search for the cell that recognizes prey
The T5 cell integration of worm features: Size Shape Movement 2 types defined by different response profiles T5(2) cells in particular produced invariant responses across changes in a number of parameters: Contrast Velocity Distance So long as the worm-like stimulus moved along its long-axis
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The T5(2) response: Putting it all together
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Antatomical and physiological organization of TH3, T5(1) and T5(2) cells
+ - Output Output options: T5(1) HIGH/ TH3 LOW = T5 (2) HIGH T5(1) HIGH/TH3 HIGH = T5(2) CANCELED T5(1) LOW/TH3 LOW = T5(2) NO INPUT/CANCELED T5(1) LOW/TH3 HIGH = T5(2) INHIBITED
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So what do you predict would happen behaviorally and in terms of T5(2) cells if you cut the output from TH3 to T5(2)? T5(1) TH3 T5(2) + - Output TH3 lesion Pre leison
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