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At least 1,153 records · Page 64Linked to original sources
PubMed2005

Is direction position? Position- and direction-based correspondence effects in tasks with moving stimuli.

Five experiments were carried out to test whether (task-irrelevant) motion information provided by a stimulus changing its position over time would affect manual left-right responses. So far, some studies reported direction-based Simon effects whereas others did not. In Experiment 1a, a reliable direction-based effect occurred, which was not modulated by the response mode--that is, by whether participants responded by pressing one of two keys or more dynamically by moving a stylus in a certain direction. Experiments 1a, 1b, and 2 lend support to the idea that observers use the starting position of target motion as a reference for spatial coding. That is, observers might process object motion as a shift of position relative to the starting position and not as directional information. The dominance of relative position coding could also be shown in Experiment 3, in which relative position was pitted against motion direction by presenting a static and dynamic stimulus at the same time. Additionally, we explored the role of eye movements in stimulus-response compatibility and showed in Experiments 1b and 3a that the execution or preparation of saccadic eye movements--as proposed by an attention-shifting account--is not necessary for a Simon effect to occur.

Adolescent↗
PubMed2001

Imaging image processing in the human brain.

Functional imaging in humans reveals the interplay of the many components of the human visual system: how they process the various types of information contained in the image to recover characteristics of the three-dimensional world surrounding us, but also how, in the course of this process, the retinal image is gradually integrated with non-retinal signals to provide information about the outside world in a format useful to other non-visual brain regions.

Animals↗
PubMed1997

Perceptual categories for spatial layout.

The central problems of vision are often divided into object identification and localization. Object identification, at least at fine levels of discrimination, may require the application of top-down knowledge to resolve ambiguous image information. Utilizing top-down knowledge, however, may require the initial rapid access of abstract object categories based on low-level image cues. Does object localization require a different set of operating principles than object identification or is category determination also part of the perception of depth and spatial layout? Three-dimensional graphics movies of objects and their cast shadows are used to argue that identifying perceptual categories is important for determining the relative depths of objects. Processes that can identify the causal class (e.g. the kind of material) that generates the image data can provide information to determine the spatial relationships between surfaces. Changes in the blurriness of an edge may be characteristically associated with shadows caused by relative motion between two surfaces. The early identification of abstract events such as moving object/shadow pairs may also be important for depth from shadows. Knowledge of how correlated motion in the image relates to an object and its shadow may provide a reliable cue to access such event categories.

Depth Perception↗
PubMed1984

Spatial contrast adaptation characteristics of neurones recorded in the cat's visual cortex.

Spatial contrast adaptation, produced by prolonged exposure to high contrast grating patterns, has become an important psychophysical method for isolating spatial and orientation selective channels in the human visual system. It has been reasonably argued that this adaptation may be fundamentally dependent upon the activity of neurones in the striate cortex. To test the validity of this hypothesis, and several others, we measured the general adaptation characteristics of 144 striate neurones using a stimulus protocol comparable to the typical psychophysical methods. In general, during prolonged high contrast stimulation, the responses of most cells exponentially decayed from a transient peak response to a sustained plateau response; following adaptation, the responses to lower contrasts were depressed relative to the unadapted state but then gradually recovered from the transient depression to a sustained plateau. Such adaptation was a property common to both simple and complex cells (the distributions of the quantitative of adaptation were overlapping); there were however small but reliable differences. We compared the neurophysiological contrast adaptation with two psychophysical estimates of human contrast adaptation (threshold contrast elevation and apparent contrast reduction) and found that the time courses and the magnitudes were quite similar. The effect of contrast adaptation on the spatial frequency tuning was assessed by measuring the contrast response function at several different test spatial frequencies before and after adaptation at the optimum centre frequency. We found that the effect of adaptation decreased as the difference between test and adaptation frequency increased. Grating contrast adaptation has been alternatively described as 'constructive gain control' on the one hand and as 'deleterious fatigue' on the other. We tested the effect of contrast adaptation on the contrast response function and found (a) that adaptation shifts the curves vertically downward parallel to the response axis (thus reflecting a decrease in the maximum rate of firing and a deleterious compression of the response range) and (b) that adaptation shifts the curves horizontally to the right parallel to the contrast axis (thus reflecting a true sensitivity shift of the remaining response range for constructive maintenance of high differential sensitivity around the prevailing background level).(ABSTRACT TRUNCATED AT 400 WORDS)

Adaptation, Ocular↗