Dynamics and robustness of familiarity memory.

When presented with an item or a face, one might have a sense of recognition without the ability to recall when or where the stimulus has been encountered before. This sense of recognition is called familiarity memory. Following previous computational studies of familiarity memory, we investigate the dynamical properties of familiarity discrimination and contrast two different familiarity discriminators: one based on the energy of the neural network and the other based on the time derivative of the energy. We show how the familiarity signal decays rapidly after stimulus presentation. For both discriminators, we calculate the capacity using mean field analysis. Compared to recall capacity (the classical associative memory in Hopfield nets), both the energy and the slope discriminators have bigger capacity, yet the energy-based discriminator has a higher capacity than one based on its time derivative. Finally, both discriminators are found to have a different noise dependence.

Optimal learning rules for discrete synapses.

There is evidence that biological synapses have a limited number of discrete weight states. Memory storage with such synapses behaves quite differently from synapses with unbounded, continuous weights, as old memories are automatically overwritten by new memories. Consequently, there has been substantial discussion about how this affects learning and storage capacity. In this paper, we calculate the storage capacity of discrete, bounded synapses in terms of Shannon information. We use this to optimize the learning rules and investigate how the maximum information capacity depends on the number of synapses, the number of synaptic states, and the coding sparseness. Below a certain critical number of synapses per neuron (comparable to numbers found in biology), we find that storage is similar to unbounded, continuous synapses. Hence, discrete synapses do not necessarily have lower storage capacity.

Effects of noise on the spike timing precision of retinal ganglion cells.

Information in a spike train is limited by variability in the spike timing. This variability is caused by noise from several sources including synapses and membrane channels; but how deleterious each noise source is and how they affect spike train coding is unknown. Combining physiology and a multicompartment model, we studied the effect of synaptic input noise and voltage-gated channel noise on spike train reliability for a mammalian ganglion cell. For tonic stimuli, the SD of the interspike intervals increased supralinearly with increasing interspike interval. When the cell was driven by current injection, voltage-gated channel noise and background synaptic noise caused fluctuations in the interspike interval of comparable amplitude. Spikes initiated on the dendrites could cause additional spike timing fluctuations. For transient stimuli, synaptic noise was dominant and spontaneous background activity strongly increased fluctuations in spike timing but decreased the latency of the first spike.