Online research in philosophy

Humans, being highly social creatures, rely heavily on the ability to perceive what others are doing and to infer from gestures and expressions what others may be intending to do. These perceptual skills are easily mastered by most, but not all, people, in large part because human action readily communicates intentions and feelings. In recent years, remarkable advances have been made in our understanding of the visual, motoric, and affective influences on perception of human action, as well as in the elucidation of the neural concomitants of perception of human action. This article reviews those advances and, where possible, draws links among those findings.Acronyms and DefinitionsApparent motion: perception of smooth motion from brief, successive exposures of static imagesChameleon effect: tendency for people to mimic the actions of others without even knowing itCommon coding principle: theory that perceiving and acting share common mental representationsDynamic noise: an array of randomly positioned dots that can camouflage perception of PL animations when the noise dots are sufficiently denseEvent-related potential (ERP): electrical brain activity registered from the scalpExtrastriate body area (EBA): brain region activated when a person views a human body or body partsFunctional magnetic resonance imaging (fMRI): widely used technique that reveals brain activation patterns based on hemodynamic responses to neural activityInversion effect: difficulty of perceiving PL animations when they are shown upside downKinematics: analysis of the motions of objects without regard to the forces producing themMirror neurons: brain cells responsive when an animal engages in an activity or when it watches another animal engaged in that activityPoint-light animations: biological activity portrayed by small light tokens (point lights) placed on the major body parts of an actorPositron emission tomography (PET): brain imaging technique that uses radioactively labeled tracers to allow visualization of active brain areasSpatiotemporal jitter: means of degrading perception of PL animations, where the relative timing and positions of the moving dots are perturbedSuperior temporal sulcus (STS): region of the cortex the posterior portion of which contains neurons selectively responsive to human activityTemplate-matching model: theory that perception of biological motion results from concatenation of static views of the bodyTranscranial magnetic stimulation (TMS): technique producing a brief disruption of neural processing.

We investigated binocular rivalry in the twocerebral hemispheres of callosotomized(split-brain) observers. We found that rivalryoccurs for complex stimuli in split-brainobservers, and that it is similar in the twohemispheres. This poses difficulties for twotheories of rivalry: (1) that rivalry occursbecause of switching of activity between thetwo hemispheres, and (2) that rivalry iscontrolled by a structure in the rightfrontoparietal cortex. Instead, similar rivalryfrom the two hemispheres is consistent with atheory that its mechanism is low in the visualsystem, at which each hemisphere conducts asimilar analysis of its half of visual space.

From the evolutionary viewpoint, animals need to monitor the surrounding environment and capture salient features, such as motion, for survival. The visual system is highly developed for monitoring a wide area of visual field and capturing such salient features. In humans and primates, there is a wide binocular field, suggesting a necessity of integrating the images from the two eyes. Binocular rivalry [R. Blake, A neural theory of binocular rivalry, Psychol. Rev. 96 (1989) 145–167; R. Blake, N.K. Logothetis, Visual competition, Nat. Rev. Neurosci. 3 (2002) 13–21], where incompatible inputs from the two eyes compete to emerge in the subject’s visual percept, has been shown to exhibit highly adaptive behavior [I. Kovacs, T.V. Parathomas, M. Yang, A. Feher, When the brain changes its mind: interocular grouping during binocular rivalry. Proc. Natl. Acad. Sci. U.S.A. 93 (1996) 15508–15511; N.K. Logothetis, Single units and conscious vision, Philos. Trans. R. Soc. Lond. B. Biol. Sci. 353 (1998) 1801–1818]. Here we investigated the spatio-temporal dynamics of the ocular dominance pattern in binocular rivalry under conditions where conflicting salient features were presented in a temporally varying manner. We found a striking example of the detailed structure of the dominance wave propagation, by using a spatio-temporal sampling method. The data show in detail the ability of the visual system to dynamically adapt to the changing stimuli in the context of the massively parallel visual field. We show by model prediction that the globally coherent dominance change in the presence of multiple stimuli can be explained by a mechanism based on local saliency comparison. © 2005 Elsevier Ireland Ltd. All rights reserved.

The neural basis of binocular rivalry has beenthe subject of vigorous debate. Do discrepantmonocular patterns rival for awareness becauseof neural competition among patternrepresentations or monocular channels? In thisarticle, I briefly review psychophysical andneurophysiological evidence pertaining to boththeories and discuss important new neuroimagingdata which reveal that rivalry is fullyresolved in monocular visual cortex. These newfindings strongly suggest that interocularcompetition mediates binocular rivalry and thatV1 plays an important role in the selection ofconscious visual information. They furthersuggest that rivalry is not a unitaryphenomenon. Interocular competition may fullyaccount for binocular rivalry whereas aseparate mechanism involving patterncompetition likely accounts for monocular andstimulus rivalry.

A midbrain neural basis for the perceptualoscillations of binocular rivalry is suggestedon the basis of fMRI studies of rivalry andinferences from the properties of rivalry thatcannot be explained from the known propertiesof primary visual cortical (V1) neurons. Therivalry switch is proposed to activatehomologous areas of each cerebral hemispherealternately, by means of a bistable oscillatorcircuit that straddles the midline of theventral tegmentum. This bistable oscillatoroperates at the same slow rate that ischaracteristic of perceptual rivalryalternations. Whilst attempting to divert thepresent preoccupation with cortical mechanismsfor rivalry, the new proposal integrates manycortical areas, in keeping with recent evidencethat binocular rivalry involves widespreadareas of the hemispheres. By linking rivalry tointerhemispheric switching mechanisms in thisway, the new proposal for the switch makes theprediction that binocular rivalry will besubject to high level influences such as moodand motivation. These predictions are beingfulfilled, with rivalry playing an increasingrole in the diagnosis and understanding if mooddisorders, schizophrenia and other psychiatricconditions.

A number of studies in the apparent motion literature were examined using the cognitive penetrability criterion to determine the extent to which beliefs affect the perception of apparent motion. It was found that the interaction between the perceptual processes mediating apparent motion and higher order processes appears to be limited. In addition, perceptual and inferential beliefs appear to have different effects on perceived motion optimality and direction. Our findings suggest that the system underlying apparent motion perception has more than one stage and is informationally encapsulated from cognitive factors.

When our visual system is confronted with ambiguous stimuli, the perceptual interpretation spontaneously alternates between the competing incompatible interpretations. The timing of such perceptual alternations is highly stochastic and the underlying neural mechanisms are poorly understood. Here, we show that perceptual alternations can be triggered by a transient stimulus presented nearby. The induction was tested for four types of bistable stimuli: structure-from-motion, binocular rivalry, Necker cube, and ambiguous apparent motion. While underlying mechanisms may vary among them, a transient flash induced time-locked perceptual alternations in all cases. The effect showed a dependency on the adaptation to the dominant percept prior to the presentation of a flash. These perceptual alternations show many similarities to perceptual disappearances induced by transient stimuli (Kanai & Kamitani, 2003, Moradi & Shimojo, 2004). Mechanisms linking these two transient induced phenomena are discussed.