Behavioral measures of sound perception and discrimination
It is well known that humans and other animals discriminate tonal frequencies in natural sounds including vocalizations. However, less is known about how they discriminate temporal cues in sound including cues that contribute to perception of tempo, timbre and loudness. Research teams in the Read lab are training rats to initiate operant behavior (start trial, top left) and to discriminate target sounds played from an overhead speaker (discriminate sound for reward, top right). With this task we find rats readily discriminate sound tempo for strawberry protein shake for reward. We are currently examining the time scales rats use to discriminate various vocal communications.
Neuron spiking patterns encode sound shape and rhythm
It was previously thought that cortical neurons keep track of sound rhythms by ticking off one spike with each beat of the rhythm like the tick-tock of a metronome. We discovered that some cortical neurons spike with a sustained “jitter” that follows the sound envelope change over time. To illustrate this we play a shaped burst of noise from our speakers (top left, sound pressure wave) and for ten trials and record all the spikes from a single cortical neuron (colored dots each spike time). We perform a cross-correlation of all spike times to generate an averaged cross correlation function (autocorrelogram) that we fit (red line) with a modified Gaussian model to estimate the reliability and jitter (derived from its area and width). The regular pattern in the autocorrelogram indicates a consistent spike timing pattern. When we quantify the width of our autocorrelogram fit we find it increases with the duration of noise bursts in our sound sequence. This is significant because it supports the theory that the spike timing pattern provide a “temporal code” of sound envelop shape and rhythm. (Lee et al., J Neurophysiology 2016).
Parallel Thalamoco-Cortical Sound Processing Pathways
At first glance, one may think that all sound processing cortices are wired up to process sound the same way. However, we find this is not the case. For example, we find separate populations of neurons form thalamic pathways to A1 and cSRAF. The pathway to A1 has genes encoding for two glutamate transporters (see blue colored pathway above); whereas the pathway to cSRAF expresses only one (see orange colored pathway above). We think these different gene expression patterns allow the pathways to encode sound with different tone frequency and timing resolution. This is significant because it suggests gene expression reflects neural functionality (Storace et al., J Neuroscience, 2010).
Undergraduate Student Projects
Majors: Physiology and Neurobiology, Electrical Engineering
Project Title: Stimulation Coding for an Auditory Midbrain Implant
Committee: Heather Read, Psychology Behavioral Neuroscience (chair), Joseph LoTurco, Physiology & Neurobiology, and Monty Escabi, Electrical & Computer Engineering
Major: Physiology and Neurobiology (2015)
Project Title: Discrimination of Temporal Cues in Rat Call Sequences