| Literature DB >> 24834061 |
Timo Stein1, Philipp Sterzer2.
Abstract
Entities:
Keywords: continuous flash suppression; interocular suppression; process dissociation; unconscious processing; visual awareness
Year: 2014 PMID: 24834061 PMCID: PMC4018522 DOI: 10.3389/fpsyg.2014.00387
Source DB: PubMed Journal: Front Psychol ISSN: 1664-1078
Figure 1Competing models of the processes mediating detection performance in the b-CFS paradigm. (A) The single-process model posits that both the CFS and the control condition measure differences between stimuli in accessing awareness that exist independent of the application of CFS, i.e., that are caused by non CFS-specific processing differences (green boxes and bars). The bar graphs on the right show how the single-process model would account for hypothetical detection differences (ΔDetection in arbitrary units) between two stimuli in the CFS condition (top) and in the control condition (bottom). To account for simple and sensitivity dissociations, the single-process model would need to assume that the CFS condition represents a more sensitive measure of non CFS-specific processing differences than the control condition. The single-process model cannot account for double dissociations. (B) The dual-process model posits that differences in conscious detection between stimuli obtained in the CFS condition are at least partly due to the application of CFS, i.e., they reflect CFS-specific processing differences (red boxes and bars). In the b-CFS literature, simple and sensitivity dissociations between the CFS and the control condition have been take to support the dual-process model. The dual-process model assumes that CFS-specific processing accounts for effects that are larger in the CFS than in the control condition, as illustrated by the red bar graphs on the right. We, however, suggest that double dissociations between the two conditions (i.e., some experimental manipulation has opposite effects on detection in the CFS and the control condition) are required to refute the single-process model and to postulate distinct CFS-specific processing.