Mechanisms for precuing superiority in visual recognition

Superior recognition, when similar alternatives are studied prior to brief target pictures of common objects, is usually attributed to selective feature analysis, which is beneficial only when the target is not readily discriminable in the alternatives. The present study found equal precuing superiority, however, for similar and dissimilar alternatives with abstract geometric stimuli, and with pictures of common objects, precuing superiority occurred only when each alternative represented the same semantic category. Precuing effects did not appear when different categories were represented in the alternatives, and performance was similar to other conditions in which only a categorical match between target and alternatives was possible. These results suggest that selective feature analysis and precuing superiority only occur when the target cannot be identified by its semantic category. With dissimilar alternatives activation of the target's category can be used to select a response, and there is no benefit from precuing.     

Predicting Divorce among Newlyweds from the First Three Minutes of a Marital Conflict Discussion

This study tested the hypothesis that how a discussion of a marital conflict begins--in its first few minutes--is a predictor of divorce. The marital conflict discussion of 124 newlywed couples was coded using the Specific Affect Coding System, and the data were divided into positive, negative, and positive-minus-negative affect totals for five 3-minute intervals. It was possible to predict marital outcome over a 6-year period using just the first 3 minutes of data for both husbands and wives. For husbands this prediction improved as the groups diverged in the remaining 12 minutes; for wives the prediction remained equally powerful for the remaining 12 minutes as it had been in the first 3 minutes.     

Visual adaptation to tilt and displacement: Sameor different processes?

Visual adaptation to tilt and displacement were compared to test whether they were dependent on the same or different processes. Although interocular transfer was essentially complete for both transforms, marked differences occurred between the two kinds of optical transforms in terms of rate of adaptation as a function of exposure time and transform magnitude, level of compensation, and rate of decay. Tilt and displacement appear to be quantitatively different, consistent with the idea of a different locus for each adaptation effect. This conclusion was supported by the absence of a correlation between individual performance under the two transforms. The possibility is discussed that displacement and tilt adaptation involve independent visual systems for the perception of location and form.     

Adaptive mechanisms in perceptual-motor coordination: components of prism adaptation

Aftereffect measures of visual shift and proprioceptive shift were obtained for prism exposure conditions in which, at the end of a sagittal pointing movement, most of the arm was visible (concurrent exposure) or only the first finger joint was visible (terminal exposure). Intermediate exposure conditions permitted view of the hand or the first two finger joints. Under the concurrent exposure condition, proprioceptive shift was greater than visual shift but, as view of the pointing hand decreased, the relative magnitude of the two components gradually reversed so that, under the terminal exposure condition, visual shift was greater than proprioceptive shift. These results are discussed in terms of a model of perceptual-motor organization (Redding, Clark, & Wallace, 1985) in which the direction of coordinative linkage between eye-head and hand-head systems determines the locus of discordance and adaptive recalibration.     

Generalization of prism adaptation

Prism exposure produces 2 kinds of adaptive response. Recalibration is ordinary strategic remapping of spatially coded movement commands to rapidly reduce performance error. Realignment is the extraordinary process of transforming spatial maps to bring the origins of coordinate systems into correspondence. Realignment occurs when spatial discordance signals noncorrespondence between spatial maps. In Experiment 1, generalization of recalibration aftereffects from prism exposure to postexposure depended upon the similarity of target pointing limb postures. Realignment aftereffects generalized to the spatial maps involved in exposure. In Experiment 2, the 2 kinds of aftereffects were measured for 3 test positions, one of which was the exposure training position. Recalibration aftereffects generalized nonlinearly, while realignment aftereffects generalized linearly, replicating Bedford (1989, 1993a) using a more familiar prism adaptation paradigm. Recalibration and realignment require methods for distinguishing their relative contribution to prism adaptation.