The perception of emotionally toned sentences by right hemisphere-damaged and aphasic subjects

The perception of 60 emotionally toned sentences, divided into meaningful and meaningless utterances, by high- and low-verbal aphasics and right hemisphere-damaged subjects who were not aphasic was investigated. The intended moods were happiness, sadness, and anger. Results indicated (a) significant differences between the aphasic groups in identifying the intended emotion but none between groups in identifying the intended emotion but none between either of these groups and the right hemispheric dysfunction subjects; (b) sentence meaningfulness only affected the responses of high-verbal aphasics; and (c) while the happy mood seemed to be the least frequently selected among the three moods, closer inspection indicated that the subjects in absence of response bias were distinguishing among the three moods with equal success.     

Imitation as a function of response commonality,serial order,and vicarious punishment

The effects of response commonality, serial order of modeled responses, and vicarious punishment on young boys' recall and acceptance of 20 commodity prefereces of an adult were examined in a 2 (common dimension vs no-common dimension) × 2 (vicarious punishment vs no-vicarious consequences) × 2 (recall or acceptance test) × 5 (response-block) factorial experiment. As predicted, the presence of a common dimension resulted in improved recall of the modeled responses, vicarious punishment was more effective under common dimension than no-common dimension conditions, and a serial order effect for recall of the modeled responses was obtained. The overall pattern of results is discussed in terms of the conceptualization that imitation requires both that the observer (1) has acquired and retained the model's responses and (2) has been placed in circumstances which favor activating this learning into overt performance.     

Are there developmental differences in reality-monitoring?

The question addressed by the present experiment is whether the ability to distinguish between veridical and imaginal memory representations changes with age. Second-grade, fourth-grade, and sixth grade children (8, 10, and 12 years old) and college students were shown pictures of familiar objects. Each picture was presented one, two, or three times and, interspersed with these presentations, subjects were asked to imagine each picture zero, one, or three times. Subsequently they were asked to judge the presentation frequency of each picture. For all groups, imagining the pictures resulted in inflated estimates of event frequency. However, contrary to the idea that children have a particularly difficult time discriminating externally generated from internally generated memories, one analysis indicated adults were actually somewhat more affected than children by the imagination trials.     

Intentional communication in the chimpanzee: The development of deception

Communication about the location of a hidden incentive was studied in chimpanzee-human dyads, in which each member of a pair served alternately as “sender” and “recipient” of information. When the human cooperated with the chimpanzee in finding the goal, from the very beginning the chimpanzees were able to produce and comprehend behavioral cues which conveyed accurate locational information. When the human and chimpanzee competed for the goal, the chimpanzees learned both to withhold information or mislead the recipient, and to discount or controvert the sender's own misleading cues. The chimpanzee's ability to convey and utilize both accurate and misleading information, by taking into account the nature of the sender or recipient, provides evidence of a capacity for intentional communication in this nonhuman primate species.     

Sampling and decision rules used by honey bees in a foraging arena

Animals must continuously choose among various available options to exploit the most profitable resource. They also need to keep themselves updated about the values of all available options, since their relative values can change quickly due to depletion or exploitation by competitors. While the sampling and decision rules by which foragers profitably exploit a flower patch have attracted a great deal of attention in theory and experiments with bumble bees, similar rules for honey bee foragers, which face similar foraging challenges, are not as well studied. By presenting foragers of the honey bee Apis cerana with choice tests in a foraging arena and recording their behavior, we investigate possible sampling and decision rules that the foragers use to choose one option over another and to track other options. We show that a large part of the sampling and decision-making process of a foraging honey bee can be explained by decomposing the choice behavior into dichotomous decision points and incorporating the cost of sampling. The results suggest that a honey bee forager, by using a few simple rules as part of a Bayesian inference process, is able to effectively deal with the complex task of successfully exploiting foraging patches that consist of dynamic and multiple options.