Responding to a target's current (probe trial) location is slower when it appears at a former distractor-occupied position (i.e., ignored-repetition [IR] trial), relative to when it arises at a new location (i.e., control trial). This RT(IR) > RT(Control) inequality defines the spatial negative priming (SNP) effect in latency terms. It is uncertain whether the elevated RT(IR) is due to the inhibition of the distractor-occupied location or to the inhibition of this location's assigned manual response (SNP locus issue). The main aim here was to examine the SNP locus issue. Notably, our SNP design used centrally presented visual events and included having two locations share a common response (many:1 location-to-response mapping) and the use of informative (70 % validity) or uninformative probe-trial response cues. The many:1 mapping trials allowed for the detection of location and response inhibition presence. Results showed that the latter, but not the former, causes inhibitory aftereffects (e.g., SNP) following uninformative response cues. Consistent with this finding, when the informative response cue was valid and was assigned to the many:1 probe response that had just served as the prime distractor response, inhibitory aftereffects were eliminated, when the probe target appeared at the prime distractor position (IR trial) or at a new location (distractor-response repeat trial). Blocked retrieval of stored distractor-processing representations was proposed as the mechanism for inhibitory aftereffect prevention.
Younger (M = 21 years) and older (M = 74 years) adults completed a spatial negative priming (SNP) task where (central) events (i.e., target or distractor) are presented in trial pairs: first the prime and then the probe. Free-choice trials were included (1 location: 2 permissible responses), which allowed us to isolate response inhibition and its consequent inhibitory aftereffects (i.e., current inhibition interferes with later related processing-e.g., SNP). The inhibitory aftereffects associated with the suppression of responses activated by distractor-occupied locations were highly comparable for younger and older adults; including similar SNP effect sizes, a significant tendency to select against former distractor (inhibited) responses (within-hand finger options) on free-choice trials, and latency delays attributable solely to the use of self-selected distractor responses. Aftereffects generated by target-occupied prime trials locations were also the same for both age groups; recently executed target responses were selected for and produced faster responding (within hand). Aftereffects were absent on between-hand free-choice trials and, overall, response selection determinants on free-choice trials matched for older and younger adults.
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