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Visual adaptation and 7T fMRI reveal facial identity processing in the human brain under shallow interocular suppression
2021, NeuroImageCitation Excerpt :Due to interocular contrast normalization in the primary visual cortex (Moradi and Heeger, 2009), higher CFS contrast in one eye would reduce the V1 response to the face stimuli presented to the fellow eye. It has been shown that adaptation to low level visual features could survive interocular suppression (Blake and Fox, 1974; Lehmkuhle and Fox, 1975; Montaser-Kouhsari et al., 2004; O'Shea and Crassini, 1981; Rajimehr, 2004; White et al., 1978). It was also reported that when the adapting and test faces were presented in the same size and location to the same eye, face shape adaptation was detected from interocularly suppressed faces (Stein et al., 2011), presumably due to adaptation of low level features.
Size-invariant but location-specific object-viewpoint adaptation in the absence of awareness
2019, CognitionCitation Excerpt :Many studies have shown that invisible visual stimuli could be processed and evoked robust neural responses as well as perceptual consequences. Prolonged exposure to simple or basic visual properties (e.g., contrast and orientation) presented without awareness resulted in visual aftereffects (Blake & Fox, 1974; He & MacLeod, 2001; He, Cavanagh, & Intriligator, 1996; Lehmkuhle & Fox, 1975), indicating neural adaptation could occur without awareness. Such unconscious processing is not limited to simple or low-level visual features, but could extend to complex visual stimuli (Alais & Blake, 1999; Montoro, Luna, & Ortells, 2014; Moore & Egeth, 1997; Wang, Weng, & He, 2012) as well as semantic information (e.g., words) (Jiang, Costello, & He, 2007).
The temporal course of recovery from brief (sub-second) adaptations to spatial contrast
2012, Vision ResearchCitation Excerpt :Despite our statistical analysis revealed a better fit for exponential models, it is worth to note that our findings support also the presence of multiple models describing the recovery from sub-second adaptations to spatial contrast. There is indeed psychophysical evidence that the recovery from contrast adaptation is better described by power functions (Greenlee et al., 1991; Magnussen & Greenlee, 1985; Rose & Evans, 1983; Rose & Lowe, 1982), whereas the recovery of other forms of adaptation (e.g., motion) is better described by exponential decay models with the recovery time proportional to the square root of adaptation time (Hershenson, 1989; Lehmkuhle & Fox, 1975; Rose, 1992). However, there is evidence of multiple models (i.e., power and exponential) also for recovery from long adaptation durations to spatial contrast (see Bodinger, 1978; Lorenceau, 1987).
Chromatic induction from surrounding stimuli under perceptual suppression
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