CNS 246: Multiunit Recording Project Proposal Evaluation of Noise Correlation in Simultaneously Recorded Neurons Alejandro Backer October 20, 1996 Neuronal responses to successive, spaced, presentations of any given stimulus vary from trial to trial. This variation has traditionally been represented as the result of noise superimposed on the stimulus signal. Alternatively, the variation could represent the multiplexing of other signals not directly related to the experimenters' stimulus. Of course, one could take the view that if a group of cells are to represent a certain stimulus parameter, then any variation in response due to other signals is just noise with respect to the represented signal. The only valid distinction, I believe, is whether the other signals are read by downstream neurons or not. If variation is not used (read) by the brain, we can call it noise for the process of extracting the signals the brain does use. If the variation is used, then noise is just a euphemism for our ignorance. Another related issue is whether the noise, if the inter-trial variation can be called noise, is correlated among different neurons. This has implications for the possibility of averaging out such noise by pooling the responses of a population of neurons, and the number of neurons that could be usefully included in such a pooling population. This correlation could also tell us something about whether the variability carries information or not. If the noise was independent from neuron to neuron, it would appear most likely that it was noise, independently generated in each neuron. If, instead, the variability was due to some factor related to the state of the animal or to some uncontrolled stimulus property, then one would expect that a deviation from the average response of one cell would be accompanied by a deviation from the average response (averaged over trials) of another cell. Recordings simultaneously obtained by Mike Wehr from pairs (and some triplets) of neurons of the antennal olfactory lobe of the locust during olfactory stimulation provide us with the possibility of addressing these questions directly. Any one of these cells shows markedly similar responses over repeated presentations of any given odor. These responses are different from cell to cell, and from odor to odor. However, the consistency of response for different trials of the same odor is not absolute: there is some variability, which has been characterized by saying that the neurons exhibit given probabilities of spiking during each of the cycles of a periodic population activity that occurs transiently in response to odor presentation. I plan to rate each spike train (each neuron, each trial) with respect to how much it deviated from the typical spike train, as defined by the PSTH. The rating of each spike train would be given by the multiplication, for all time bins, of the probability of that neuron firing in that time bin(averaged over all trials for that neuron) for all the time bins in which a spike occurred in that spike train, times the trial-averaged probability of the neuron not firing during that time bin for all time bins in which a spike did not occur. Thus, spike trains resembling the average spike train will get a larger rating than those differing substantially. I will then correlate the "typicality" ratings for simultaneously recorded cells as a function of trial, i.e. I will test whether atypical response in one cell is accompanied beyond chance-level by atypical response of another cell during that same trial. This will assess the independence of what is currently considered to be noise in the neural response of these neurons, establish the degree of noise correlation, and possibly illuminate us with regard to the noise versus information question of neuronal response variability.