, 2011). In addition, experimental work linking selleck chemicals intracortical synaptic connectivity to noise correlations (Ko et al., 2011) suggests that local circuit mechanisms may also contribute to the relationship between signal and noise correlation. In our case, because the same population of CLM neurons can represent different stimuli using qualitatively different correlation structures, the circuitry (local or extrinsic) that controls the correlation structure must be flexible on a short timescale. Further

experiments will be necessary to elucidate the circuitry that yields this stimulus-specific flexibility. Our results also provide initial evidence that flexibility in the relationship between signal and noise correlations is cell type specific. For example, the correlations in the pooled population of NS-NS and NS-WS pairs did not exhibit the same effects as the WS-WS pairs (Figure S3C). This suggests that the plasticity of the correlation structure primarily exists within WS (putative excitatory) neurons, although more data are necessary. One possible explanation of this is that WS-WS pairs receive less common input than NS-NS pairs or NS-WS pairs, and thus their interneuronal correlations are http://www.selleckchem.com/products/NVP-AUY922.html most susceptible to modulation by local circuitry. Such an idea is supported by findings that noise correlations are higher among inhibitory interneurons than

excitatory neurons (Constantinidis and Goldman-Rakic, 2002) and that the slope of the relationship between signal and noise correlations is much shallower for pairs of excitatory pyramidal neurons than for pairs of inhibitory parvalbumin-expressing neurons in primary visual cortex (Hofer et al., 2011). Our results suggest that large neural populations in CLM better discriminate differences between task-relevant motifs than

between task-irrelevant or novel motifs. CLM provides auditory information directly to HVC (Bauer et al., 2008), a region known to control song production (Long and Fee, 2008; Nottebohm et al., 1976). The enhanced population coding in CLM may influence the flow of auditory feedback into HVC during juvenile song learning and for adult song maintenance, two behaviors critical for survival, by selectively emphasizing the most important motifs. This possibility could Amine dehydrogenase be explored by chronically recording from CLM populations during these behaviors. We demonstrate that the relationship between signal and noise correlations is a target of learning-dependent plasticity that can substantially enhance the representation of specific stimuli. Moreover, the effects of this plasticity on neural coding increase substantially with population size, becoming quite considerable once the population reaches five to six neurons. Our results support the longstanding hypothesis that these activity patterns underlie behaviorally relevant discrimination of sensory signals (Oram et al., 1998).