on the notion of interaction of the specific and nonspecific afferent visual systems is presented. Discussionis focused on nonmonotonicmasking functions. In particular, it is proposed that in order for visual information (patterns, forms, etc.) to be consciously perceived,both specificretina-genicula-striate impulses and nonspecificretina-reticulacortical impulses should converge in the same cortical space. Nonspecific activity is shown to be necessary for subjective awareness. This activity is shown to be of longer latency than specificactivity. It is concluded that trailing conscious-experience-generating impulses are elicited by collateral activity from the specific information received from the first stimulus. These impulses reach the cortex at the same moment as the specific activity of the second (masking)stimulus as coded,whichhas a relatively higher signal-to-noise ratio in the given retinotopically specJfied cortical space. Consequently, subjects consciously perceive the second stimulus. This operation of awareness generation is termed perceptual retouch and is considered as a special psychologicalmechanism worthy of psychophysical study.Classical works in the physiology of arousal and nonspecific sensory systems have proved convincingly that the neurophysiological substrate necessary for energizing the brain and providing sufficient activity for the manifestation of conscious experience (perceptual awareness) is located subcortically and consists of the brainstem reticular formation and nonspecific thalamic activating system (Dixon, 1971; Jasper, Proctor, Knighton, Noshay, & Costello, 1958;Magoun, 1958;Riklan& Levita, 1969;Smirnov, Muchnik, & Shandurina, 1978; Worden, Swazey, & Adelman, 1975).The importance of energetic, rather than purely structural or algoristic, processes in visual masking and information processing is rarely stressed. It has been shown, however, that percepts evolve and accumulate over time (Eriksen & Schultz, 1978). This perceptogenetic or microgenetic process takes a relatively long time (see Bachmann, 1977Bachmann, , 1980Flavell & Draguns, 1957;Kahneman & Norman, 1964;Kragh & Smith, 1970; Lange, 1893;Nikitin, 1905;Vekker, 1974). Furthermore, the time for specific impulses to reach the highest levels of the nervous system is much shorter than the whole microgenetic process. Thus, we have reason to believe that, first, much of this evolution of subjective experience ofThe author wishes to convey his sincerest thanks to Professor Charles W. Eriksen for his most generous help in making this article more idiomatic and succinct. The author's mailing address is: Department of Psychology, Tartu State University, 78 Tiigi Street, Tartu, Estonian SSR, 202400 U.S.S.R. the presented actual input consists of heterarchic cyclic activity rather than purely of afference, and, second, the temporally trailing nonspecific sensory activities playa crucial role in this process.The present article will argue that, in visual masking, the interaction of specific sensory systems with nonspecific "ene...