The value of the SAC at 0 ms lag is termed the correlation index, and it describes the propensity for a neuron to spike with submillisecond precision across multiple presentations of the same song, with a value of 1 indicating chance and larger values indicating greater degrees of trial-to-trial precision. BS neurons in the higher-level AC had significantly higher correlation

index values (10.3 ± 13.0) than did midbrain, primary AC, or higher-level AC NS neurons (correlation indexes of 2.8 ± 3.1; 2.5 ± 1.9; and 2.1 ± 0.7, respectively; Figure 2E). Also in contrast to other populations, BS neurons were typically driven by a subset of songs (6.9 ± 5.2 out of 15), while midbrain, primary AC, and higher-level AC NS neurons

responded BLU9931 concentration to nearly every song (14.4 ± 2.5; 14.7 ± 1.9; and 14.96 ± 0.21 out of 15, respectively). We quantified response selectivity Entinostat mouse as 1 − (n/15), where n was the number of songs to which an individual neuron reliably responded. BS neurons in the higher-level AC were significantly more selective than were neurons in other populations (Figure 2F). Broad and narrow populations of neurons in the midbrain and primary AC did not differ in the neural coding of song (Figure S4). Furthermore, we found no systematic relationship between response properties of primary AC neurons and anatomical location ADAMTS5 along the dorsal-ventral or anterior-posterior axes,

each of which correlates with the location of subregions (Figure S5). Together, these results show that the neural coding of song changes minimally between the midbrain and primary AC, but a stark transformation in song coding occurs between the primary AC and BS neurons in the higher-level AC. As a population, BS neurons represented songs with a sparse and distributed population code, in contrast to neurons in upstream areas. The BS neurons driven by a particular song each produced discrete spiking events at different times in the song (Figure 3A), resulting in a sparse neural representation that was distributed across the population. We quantified population sparseness by measuring the fraction of neurons in each population that were active during a sliding window of 63 ms, which is the average duration of a zebra finch song note (the basic acoustic unit of song; see spectrogram in Figure 3A). While more than 70% of neurons in upstream auditory areas fired during an average 63 ms window, fewer than 5% of BS neurons were active during the same epoch (Figure 3B). Despite the markedly different population coding of song in the BS population compared to the NS and upstream populations (Figure S3), the temporal pattern produced by the BS population was similar to the temporal patterns produced by the dense coding populations (Figure 3C).