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Haptic Object Localization in the Vibrissal System: Behavior and Performance

Overview
Journal J Neurosci
Specialty Neurology
Date 2006 Aug 18
PMID 16914670
Citations 112
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Abstract

Using their large mystacial vibrissas, rats perform a variety of tasks, including localization and identification of objects. We report on the discriminatory thresholds and behavior of rats trained in a horizontal object localization task. Using an adaptive training procedure, rats learned to discriminate offsets in horizontal (anteroposterior) location with all, one row, or one arc of whiskers intact, but not when only a single whisker (C2) was intact on each cheek. However, rats initially trained with multiple whiskers typically improved when retested later with a single whisker intact. Individual rats reached localization thresholds as low as 0.24 mm (approximately 1 degree). Among the tested groups, localization acuity was finest (<1.5 mm) with rats that were initially trained with all whiskers and then trimmed to one arc of whiskers intact. Horizontal acuity was finer than the typical inter-vibrissal spacing (approximately 4.8 mm at contact points). Performance correlated with the net whisking spectral power in the range of 5-25 Hz but not in nonwhisking range of 30-50 Hz. Lesioning the facial motor nerves reduced performance to chance level. We conclude that horizontal object localization in the rat vibrissal system can reach hyperacuity level and is an active sensing process: whisker movements are both required and beneficiary, in a graded manner, for making accurate positional judgments.

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References
1.
Wightman F, Kistler D . Resolution of front-back ambiguity in spatial hearing by listener and source movement. J Acoust Soc Am. 1999; 105(5):2841-53. DOI: 10.1121/1.426899. View

2.
Hamada Y, Miyashita E, Tanaka H . Gamma-band oscillations in the "barrel cortex" precede rat's exploratory whisking. Neuroscience. 1999; 88(3):667-71. DOI: 10.1016/s0306-4522(98)00468-0. View

3.
Kelly M, Carvell G, Kodger J, Simons D . Sensory loss by selected whisker removal produces immediate disinhibition in the somatosensory cortex of behaving rats. J Neurosci. 1999; 19(20):9117-25. PMC: 6782760. View

4.
Polley D, Frostig R . Two directions of plasticity in the sensory-deprived adult cortex. Neuron. 1999; 24(3):623-37. DOI: 10.1016/s0896-6273(00)81117-4. View

5.
Jenkinson E, Glickstein M . Whiskers, barrels, and cortical efferent pathways in gap crossing by rats. J Neurophysiol. 2000; 84(4):1781-9. DOI: 10.1152/jn.2000.84.4.1781. View