Baldassano, JamesSoundwaves are rapidly modulated, multi-dimensional stimuli. The cochlea decomposes these signals into frequency and intensity information which is conveyed via the auditory nerve into the brain. How does the brain manage to extract these multidimensional signals from auditory nerve activity? How does it sculpt this input so that both the microsecond precision of “where?” and the spectrotemporal modulations of “what?” are encoded with high fidelity? Birds are powerful models for studying early auditory processing because they interact with sounds similarly to mammals but have a simpler neuronal architecture. We describe the intrinsic physiology and anatomy and auditory brainstem neurons involved in spectrotemporal processing. In birds, the auditory nerve synapses onto two anatomically distinct cochlear nuclei, cochlear nucleus magnocellularis (NM) which encodes frequency/timing information, and the more heterogeneous cochlear nucleus angularis (NA) which encodes intensity information. NA has been shown to encode the acoustic envelope, likely through a subset of neurons that respond preferentially to modulations in their inputs via an adaptive spike threshold. We first examined the intrinsic basis of this adaptive threshold and found that a dendrotoxin-sensitive low threshold potassium conductance is responsible for it. In addition to the intrinsic properties of neurons, inhibition sculpts a number of auditory processes. The majority of inhibition in the avian auditory brainstem originates in the superior olivary nucleus (SON), which has multiple response types & projects either to multiple lower order ipsilateral nuclei, including NA & NM, or to the contralateral SON. Retrograde labeling experiments have demonstrated that these projections originate from distinct populations of SON neurons, however it is not clear if there is a relationship between response types and postsynaptic target. We used in vitro electrophysiology and neuronal reconstruction to establish a relationship between response types and targets. While the function of inhibition is well documented in timing circuits, its role in intensity processing is less clear. We used dynamic clamp to model inhibitory conductances while recording from NA neurons in vitro to determine how inhibition impacts the range of inputs that a NA neuron can encode before its firing rate saturates.enDissertationNeurosciencesPhysiologyNeurosciencesAuditory brainstemInhibitionKv1NeuroethologyNucleus Angularis