Do You ‘See’ What I ‘See’? Differentiation of Visual Action Words

Dickinson and Szeligo (Can J Exp Psychol 62(4):211–222, 2008) found that processing time for simple visual stimuli was affected by the visual action participants had been instructed to perform on these stimuli (e.g., see, distinguish). It was concluded that these effects reflected the differences in the durations of these various visual actions, and the results were compared to participants’ subjective ratings of word meaning but it was also possible that word characteristics like length might have influenced response times. The present study takes advantage of word length differences between French and English visual action words in order to address this issue. The goals of the present study were to provide evidence that (1) the processing time differences previously found were due to differences in the cognitive actions represented by these words (and not due to characteristics to the words themselves), and (2) that individuals subjectively differentiate visual action words in such a way that allows for predictable differences in behaviour. Participants differentiated 14 French visual action words along two dimensions. Four of these words were then used in the instructions for a size-discrimination task. Processing time depended on the visual action word in the instruction to the task and differed in a predictable manner according to word meaning but not word length.     

Resolution of outcome-induced response conflict by humans after extended training

Studies of incongruent discrimination learning, where the outcome event of one response acts as the discriminative stimulus for the opposite response, suggest that humans rely on habitual stimulus–response (S–R) associations when outcome–response (O–R) associations would cause response conflict. Here, two experiments were conducted to investigate the robustness of this habitual strategy. In Experiment 1, we found that extensive instrumental discrimination training supported learning about the incongruent R → O contingencies, as assessed by an outcome devaluation test. Differential representations of the stimulus and the (associatively retrieved) outcome may have allowed for goal-directed incongruent performance. Experiment 2 failed to provide evidence for this possibility; direct presentation as well as associative retrieval of the incongruent events (by Pavlovian stimuli) activated the response that was associated with each event in its role of stimulus as opposed to outcome. We did find that participants successfully acquired explicit knowledge of the incongruent contingencies, which raises the possibility that propositional encoding allowed them to overcome the response conflict caused by O–R associations. Alternative associative and propositional accounts of successful goal-directed incongruent performance with extensive training will be discussed.     

Relationship Between Muscle Fiber Type and Reactive Balance: A Preliminary Study

The authors’ objective was to quantify the relationship between type II muscle fiber composition and recovery latency from controlled perturbations. Thirty healthy adults performed a Thorstensson test to indirectly determine muscle fiber composition of the knee extensors. On a subsequent day, reactive balance was measured by assessing latency time required to accommodate three controlled perturbations via computerized dynamic posturography. The proportion of type II fibers had a negative correlation with latency caused by a large backward perturbation (r = –.62, p = .001). These data may indicate a higher percentage of type II fibers in the knee extensors are associated with better reactive balance. Further investigation is warranted, in particular as it pertains to populations at risk for balance impairment.     

Motivational control of instrumental performance following a shift from thirst to hunger

Thirsty rats were trained to press a lever for either a sucrose solution or saline before performance was tested in extinction while the animals were either hungry alone or experiencing both hunger and a sodium appetite. Reinforcer-specific motivational control was observed in that the animals trained with the sucrose solution pressed more than those trained with the saline when they were tested hungry, but not when they were tested under combined hunger and sodium appetite. In order to assess the role of a Pavlovian incentive process in this effect, thirsty animals received non-contingent pairings of one stimulus with the sucrose solution and another with saline in the second experiment. In an extinction test the sucrose stimulus augmented lever pressing relative to the saline stimulus when the animals were hungry, but not when they were thirsty. In the subsequent experiments the contribution of the Pavlovian process was equated by giving concurrent training with both incentives. Lever pressing and chain pulling were reinforced concurrently, one with the sucrose solution and the other with saline, while the animals were thirsty. Once again, the animals pressed more in extinction if this action had been trained with the sucrose solution rather than the saline, but only if they were hungry rather than thirsty. Thus, instrumental performance across a thirst-to-hunger shift can also be controlled by an instrumental incentive process. The direct engagement of the instrumental process by this motivational shift contrasts to the absence of such control following a hunger-to-thirst transition (Dickinson & Dawson, 1987a), a fact attributed to the asymmetrical motivational interactions produced by water and food deprivation.