An increased P1, can also be found during recognition of task irrelevant information. As an example let us consider Experiment 2 in the study by Freunberger et al. (2008a). The experiment consisted of a semantic (living/non-living) picture categorization task with Dasatinib in vivo meaningful and meaningless pictures. Meaningful pictures represent living, and non-living objects. Meaningless pictures were obtained by distorting pictures of living and non-living objects. We predict that the P1 will be larger for
distorted pictures because they can be considered task irrelevant with respect to semantic categorization. Thus, this prediction also focuses on inhibition, but not in the sense of suppressing activity in potentially interfering brain regions, but in the sense of suppressing task irrelevant processes. Distorted pictures (with no semantic meaning) may very early (on the basis of their sensory features) be categorized as semantically meaningless which allows suppression of irrelevant ‘spreading activation processes’ aiming at identifying the stimulus. The findings are in line selleck inhibitor with this interpretation and show that the P1 for meaningless
pictures is delayed and significantly larger than for the ‘task- or processing-relevant’ pictures denoting living and non-living objects (cf. Fig. 6). Most importantly we could also show that the alpha-filtered ERPs exhibit differences in the P1 range that are similar to those of the unfiltered ERPs. Finally, it should be mentioned that in go/no go tasks, where only one type of stimulus must be attended and processed, the P1 will be larger for the go- as compared to the no go-stimulus. (e.g. Rousselet et al., 2007). Another interesting finding, well in line with our theory is that increasing processing complexity (C) during early categorization is associated with an increase in P1 amplitude. Particularly for faces Interleukin-2 receptor the inversion of an image has a strong effect on task difficulty.
Thus, the increased P1 in response to inverted but also scrambled faces (e.g., Allison et al., 1999, Itier and Taylor, 2004, Linkenkaer-Hansen et al., 1998 and Sagiv and Bentin, 2001) can indeed be associated with increased processing demands during early categorization. A very similar interpretation can be applied for the encoding of words or pseudowords. Increased P1 amplitudes were found with increasing orthographic neighborhood size (N) and increasing word-length (for a review, cf. Dien, 2009). According to our hypothesis processing complexity (C) would be high in both cases leading to an increase in SNR that operates to select specific entry points into lexical memory. As a consequence, ERP amplitudes increase in the latency range of the P1. In contrast to neighborhood size and word length, word frequency and orthographic typicality decrease P1 amplitude (Hauk et al., 2006a and Hauk et al., 2006b).
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