Re-imagining motor imagery: building bridges between cognitive neuroscience and sport psychology

One of the most remarkable capacities of the mind is its ability to simulate sensations, actions, and other types of experience. A mental simulation process that has attracted recent attention from cognitive neuroscientists and sport psychologists is motor imagery or the mental rehearsal of actions without engaging in the actual physical movements involved. Research on motor imagery is important in psychology because it provides an empirical window on consciousness and movement planning, rectifies a relative neglect of non-visual types of mental imagery, and has practical implications for skill learning and skilled performance in special populations (e.g., athletes, surgeons). Unfortunately, contemporary research on motor imagery is hampered by a variety of semantic, conceptual, and methodological issues that prevent cross-fertilization of ideas between cognitive neuroscience and sport psychology. In this paper, we review these issues, suggest how they can be resolved, and sketch some potentially fruitful new directions for inter-disciplinary research in motor imagery.     

Dissociating contingency awareness and conditioned attitudes: evidence of contingency-unaware evaluative conditioning

Whether human evaluative conditioning can occur without contingency awareness has been the subject of an intense and ongoing debate for decades, troubled by a wide array of methodological difficulties. Following recent methodological innovations, the available evidence currently points to the conclusion that evaluative conditioning effects do not occur without contingency awareness. In a simulation, we demonstrate, however, that these innovations are strongly biased toward the conclusion that evaluative conditioning requires contingency awareness, confounding the measurement of contingency memory with conditioned attitudes. We adopt a process-dissociation procedure to separate the memory and attitude components. In 4 studies, the attitude parameter is validated using existing attitudes and applied to probe for contingency-unaware evaluative conditioning. A fifth experiment incorporates a time-delay manipulation confirming the dissociability of the attitude and memory components. The results indicate that evaluative conditioning can produce attitudes without conscious awareness of the contingencies. Implications for theories of evaluative conditioning and associative learning are discussed.     

Positivity effect in healthy aging in observational but not active feedback-learning

The present study investigated the impact of healthy aging on the bias to learn from positive or negative performance feedback in observational and active feedback learning. In active learning, a previous study had already shown a negative learning bias in healthy seniors older than 75 years, while no bias was found for younger seniors. However, healthy aging is accompanied by a 'positivity effect', a tendency to primarily attend to stimuli with positive valence. Based on recent findings of dissociable neural mechanisms in active and observational feedback learning, the positivity effect was hypothesized to influence older participants' observational feedback learning in particular. In two separate experiments, groups of young (mean age 27) and older participants (mean age 60 years) completed an observational or active learning task designed to differentially assess positive and negative learning. Older but not younger observational learners showed a significant bias to learn better from positive than negative feedback. In accordance with previous findings, no bias was found for active learning. This pattern of results is discussed in terms of differences in the neural underpinnings of active and observational learning from performance feedback.     

Small and large number discrimination in guppies

Non-verbal numerical behavior in human infants, human adults, and non-human primates appears to be rooted in two distinct mechanisms: a precise system for tracking and comparing small numbers of items simultaneously (up to 3 or 4 items) and an approximate system for estimating numerical magnitude of a group of objects. The most striking evidence that these two mechanisms are distinct comes from the apparent inability of young human infants and non-human primates to compare quantites across the small (<3 or 4)/large (>4) number boundary. We ask whether this distinction is present in lower animal species more distantly related to humans, guppies (Poecilia reticulata). We found that, like human infants and non-human primates, fish succeed at comparisons between large numbers only (5 vs. 10), succeed at comparisons between small numbers only (3 vs. 4), but systematically fail at comparisons that closely span the small/large boundary (3 vs. 5). Furthermore, increasing the distance between the small and large number resulted in successful discriminations (3 vs. 6, 3 vs. 7, and 3 vs. 9). This pattern of successes and failures is similar to those observed in human infants and non-human primates to suggest that the two systems are present and functionally distinct across a wide variety of animal species.     

Attachment anxiety and attentional control predict immediate and delayed emotional Stroop interference

Attachment anxiety has been associated with a hyperactivating response to threat. A modified emotional Stroop task was used to investigate temporal characteristics of the threat response by assessing response latencies to interpersonally threatening words (immediate interference) and two directly subsequent neutral filler words (delayed interference). Greater immediate and delayed interference to threatening words was observed (n = 125), with higher levels of attachment anxiety associated with immediate interference to threatening cues, and lower levels with delayed interference. Thus, attachment anxiety was related to the speed at which moderate perceived threat disrupted ongoing processes under top-down attentional control. Furthermore, top-down attentional control moderated the extent to which immediate or delayed interference was observed. Among participants who demonstrated relatively stronger top-down attentional control, immediate and delayed interference to threatening cues was minimal, suggesting that results involving emotional Stroop interference were primarily attributable to participants with relatively weaker top-down attentional control. The implications of these findings are considered within the broader context of performance-based and neuroimaging research, with suggestions for future applied research.     

Is Mental Rotation Ability a Predictor of Success for Motor Performance?

Previous studies provided evidence of a relationship between mental rotation (MR) and motor processes in children and adults. However, there is no direct evidence that MR ability is a reliable predictor of success for motor performance. After completion of a MR test, the motor performance of 7- to 8-year-old and 11- to 12-year-old children was measured along a steeple chase and an equivalent straight distance sprint. The chase involved several motor actions requiring, among different competencies, spatial abilities such as performing a forward roll, jumping, crawling, turning, and changing directions. Data revealed that the time taken to complete the chase was influenced by speed and sex, but also by the individual MR ability. Based on these findings, we assume that MR and motor performance may share similar subprocesses.     

A biologically based model for recognition of 2-D occluded patterns

In this work, we present a biologically inspired model for recognition of occluded patterns. The general architecture of the model is based on the two visual information processing pathways of the human visual system, i.e. the ventral and the dorsal pathways. The proposed hierarchically structured model consists of three parallel processing channels. The main channel learns invariant representations of the input patterns and is responsible for pattern recognition task. But, it is limited to process one pattern at a time. The direct channel represents the biologically based direct connection from the lower to the higher processing level in the human visual cortex. It computes rapid top-down pattern-specific cues to modulate processing in the other two channels. The spatial channel mimics the dorsal pathway of the visual cortex. It generates a combined saliency map of the input patterns and, later, segments the part of the map representing the occluded pattern. This segmentation process is based on our hypothesis that the dorsal pathway, in addition to encoding spatial properties, encodes the shape representations of the patterns as well. The lateral interaction between the main and the spatial channels at appropriate processing levels and top-down, pattern-specific modulation of the these two channels by the direct channel strengthen the locations and features representing the occluded pattern. Consequently, occluded patterns become focus of attention in the ventral channel and also the pattern selected for further processing along this channel for final recognition.