g., Muller-Gass et al., 2007 and Salisbury et al., 1992]). A similarly slow and late waveform is seen in MEG (van Aalderen-Smeets et al., 2006). The generators of the

P3b ERP have been shown by intracranial recordings and ERP-fMRI correlation to involve a highly distributed set of nearly simultaneous active areas including hippocampus LY2835219 mw and temporal, parietal, and frontal association cortices (Halgren et al., 1998 and Mantini et al., 2009). The P3b has been reproducibly observed as strongly correlated with subjective reports, both when varying stimulus parameters (e.g., Del Cul et al., 2007) and when comparing identical trials with or without conscious perception (e.g., Babiloni et al., 2006, Del Cul et al., 2007, Fernandez-Duque et al., 2003, Koivisto et al., 2008, Lamy et al., 2009, Niedeggen et al., 2001, Pins and Ffytche, 2003 and Sergent et al., 2005) (however, this effect may disappear when the subject already has a conscious working memory representation of the target: Melloni et al., 2011). The effect is not easily imputable to increased postperceptual processing or other task confounds, as many studies equated attention and response requirements on conscious and nonconscious trials (e.g., Del Cul et al., 2007, Gaillard et al., 2009, Lamy et al., 2009 and Sergent et al., 2005). For instance, Lamy et al. (2009) compared correct aware versus correct

unaware trials in a forced-choice localization task on a masked stimulus, thus equating for stimuli and responses, and again observed a tight correlation with the P3b component. Human ERP and MEG recordings also revealed BMS-354825 that conscious perception is also accompanied, during a similar time window, by increases in the

power of high-frequency fluctuations, primarily in the gamma band (>30 Hz), as well as their phase synchronization across distant cortical sites (Doesburg et al., 2009, Melloni et al., 2007, Rodriguez et al., 1999, Schurger et al., 2006 and Wyart and Tallon-Baudry, 2009). In lower frequencies belonging to the alpha and low beta bands (10–20 Hz), the data are more ambiguous, as both power increases (Gross et al., 2004) and crotamiton decreases (Gaillard et al., 2009 and Wyart and Tallon-Baudry, 2009) have been reported, perhaps due to paradigm-dependent variability in the deployment of dorsal parietal attention networks associated with decreases in alpha-band power (Sadaghiani et al., 2010). Even when power decreases in these low frequencies, however, their long-distance phase synchrony is consistently increased during conscious perception (Gaillard et al., 2009 and Gross et al., 2004; see also Hipp et al., 2011). The globally distributed character of these power and synchrony increases seems essential, because recent results indicate that localized increases in these parameters can be evoked by nonconscious stimuli, particularly during the first 200 ms of stimulus processing ( Fisch et al., 2009, Gaillard et al.