HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text Full Text (PDF) All Versions of this Article: 100/2/852    most recent 90300.2008v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Google Scholar Articles by Krahe, R. Articles by Chacron, M. J. PubMed PubMed Citation Articles by Krahe, R. Articles by Chacron, M. J.

Temporal Processing Across Multiple Topographic Maps in the Electrosensory System

¹Department of Biology and ²Department of Physiology, Center for Nonlinear Dynamics, McGill University, Montreal, Quebec, Canada; and ³Department of Zoology, University of Oklahoma, Norman, Oklahoma

Submitted 24 February 2008; accepted in final form 21 May 2008

Multiple topographic representations of sensory space are common in the nervous system and presumably allow organisms to separately process particular features of incoming sensory stimuli that vary widely in their attributes. We compared the response properties of sensory neurons within three maps of the body surface that are arranged strictly in parallel to two classes of stimuli that mimic prey and conspecifics, respectively. We used information-theoretic approaches and measures of phase locking to quantify neuronal responses. Our results show that frequency tuning in one of the three maps does not depend on stimulus class. This map acts as a low-pass filter under both conditions. A previously described stimulus-class-dependent switch in frequency tuning is shown to occur in the other two maps. Only a fraction of the information encoded by all neurons could be recovered through a linear decoder. Particularly striking were low-pass neurons the information of which in the high-frequency range could not be decoded linearly. We then explored whether intrinsic cellular mechanisms could partially account for the differences in frequency tuning across maps. Injection of a Ca²⁺ chelator had no effect in the map with low-pass characteristics. However, injection of the same Ca²⁺ chelator in the other two maps switched the tuning of neurons from band-pass/high-pass to low-pass. These results show that Ca²⁺-dependent processes play an important part in determining the functional roles of different sensory maps and thus shed light on the evolution of this important feature of the vertebrate brain.