Predictive joint-action model: A hierarchical predictive approach to human cooperation

Research in a number of related fields has recently begun to focus on the perceptual, cognitive, and motor workings of cooperative behavior. There appears to be enough coherence in these efforts to refer to the study of the mechanisms underlying human cooperative behavior as the field of joint-action (Knoblich, Butterfill, & Sebanz, 2011; Sebanz, Bekkering, & Knoblich, 2006). Yet, the development of theory in this field has not kept pace with the proliferation of research findings. We propose a hierarchical predictive framework for the study of joint-action that we call the predictive joint-action model (PJAM). The presentation of this theoretical framework is organized into three sections. In the first section, we summarize hierarchical predictive principles and discuss their application to joint-action. In the second section, we juxtapose PJAM’s assumptions with empirical evidence from the current literature on joint-action. In the third section, we discuss the overall success of the hierarchical predictive approach to account for the burgeoning empirical literature on joint-action research. Finally, we consider the model’s capacity to generate novel and testable hypotheses about joint-action. This is done with the larger goal of uncovering the empirical and theoretical pieces that are still missing in a comprehensive understanding of joint action.     

Rapid resumption of interrupted search is independent of age-related improvements in visual search

In this study, 7-19-year-olds performed an interrupted visual search task in two experiments. Our question was whether the tendency to respond within 500 ms after a second glimpse of a display (the rapid resumption effect [Psychological Science, 16 (2005) 684-688]) would increase with age in the same way as overall search efficiency. The results indicated no correlation of rapid resumption with search speed either across age groups (7, 9, 11, and 19 years) or at the level of individual participants. Moreover, relocating the target randomly between looks reduced the rate of rapid resumption in a very similar way at each age. These results imply that implicit perceptual prediction during search is invariant across this age range and is distinct from other critical processes such as feature integration and control over spatial attention.     

How much like a target can a mask be? Geometric, spatial, and temporal similarity in priming: a reply to Schlaghecken and Eimer (2006)

The authors make 3 points in response to F. Schlaghecken and M. Eimer's proposal of self-inhibition as an explanatory factor in the negative compatibility effect: (a) The self-inhibition hypothesis lacks empirical support for its main tenets; (b) considering the roles of geometric, spatial, and temporal similarity of primes and masks makes self-inhibition unnecessary; and (c) the negative compatibility effect occurs even when the main tenets of self-inhibition are violated. The authors propose that understanding what is "relevant" in a masked-priming task applies not only to geometric features that are shared with the target but to spatial and temporal ones as well. Briefly, target-mask similarity determines how motor preparation is accumulated during the prime-mask sequence.     

Subjective well-being is heritable and genetically correlated with dominance in chimpanzees (Pan troglodytes)

The hypothesis that subjective well-being (SWB) is heritable and genetically correlated with Dominance was tested using 128 zoo chimpanzees. Dominance was a chimpanzee-specific personality factor including items reflecting Extraversion and low Neuroticism. SWB was measured with a 4-item scale. The best behavior genetic model included additive genetic and nonshared environmental effects for SWB and Dominance, marginal matemal effects for SWB, a high genetic correlation, and a low nonshared environmental correlation. Results indicated that the shared variance between SWB and Dominance was a consequence of common genes and that the unique variance between SWB and Dominance was a consequence of the nonshared environment. These findings indicate that common genes may underlie the correlation between human personality factors and SWB.     

Visual binding in the standing wave illusion

When two video frames are alternated at the appropriate rate, one with a central bar and the other with two flanking bars, the central bar becomes invisible. Competing explanations for this standing wave illusion are examined, with the results showing an influence of higher level shape representations on lower level edge processes. In Experiment 1, flanking bar duration was found to be more important to masking than central bar duration. Experiment 2 showed strong nonlocal effects in that masking of the central bar depended critically on whether it appeared in the same video frame as other visible bars. Experiments 3 and 4 showed that the contour shared by bars in separate frames was a less important factor than shape and surface similarity. This illusion is therefore an excellent tool for studying recursive interactions between higher level object representations and lower level contour processes.     

Attentional requirements is visual detection and identification: evidence from the attentional blink

Perception of the 2nd of 2 targets (T1 and T2) is impaired if the lag between them is short (0-500 ms). The authors used this attentional blink (AB) to index attentional requirements in detection and identification tasks, with or without backward masking of T2, in 2 stimulus domains (line orientation, coherent motion). With masking, the AB occurred because T2 was masked during the attentional dwell time created by T1 processing (Experiments 1, 2, and 3). Without masking, an AB occurred only in identification because during the attentional dwell time, T2 decayed to a level that could support simple detection but not complex identification. However, an AB occurred also in detection if T2 was sufficiently degraded (Experiment 4). The authors drew 2 major conclusions: (a) Attention is required in both identification and detection, and (b) 2 factors contribute to the AB, masking of T2 while attention is focused on T1 and decay of the T2 trace while unattended.     

Psychological vulnerabilities in patients with major depression vs panic disorder

The tripartite model (Clark & Watson, 1991: Clark, L. A., & Watson, D. (1991). Tripartite model of anxiety and depression: Psychometric evidence and taxonomic implications. Journal of Abnormal Psychology, 100, 316-336) posits that anxiety and depression share nonspecific features of neuroticism but that somatic arousal appears unique to anxiety, and low positive affect appears unique to depression. The present study controlled for these higher-order effects and evaluated the relative contributions of four, specific lower-order vulnerabilities (anxiety sensitivity, rumination, self-criticism, self-oriented perfectionism). Participants were 38 depressed patients and 38 patients with panic disorder matched as closely as possible for age and gender, and all were diagnosed using the same structured interview by an experienced clinician. Results from hierarchical logistic regression analysis were consistent with predictions from the tripartite model in that only the unique features of arousal and positive affectivity differentiated the two diagnostic groups. At a lower-order level, only anxiety sensitivity (and its facet of fear of physical symptoms) and a ruminative response style demonstrated incremental predictive ability. The discussion focuses on the relationships among these higher-order and lower-order variables, and their potential importance for understanding specific manifestations of psychopathology.     

Task switching mediates the attentional blink even without backward masking

When two targets are presented in rapid succession, perception of the second target is impaired at short intertarget lags (100-700 msec). This attentional blink (AB) is thought to occur only when the second target is backward masked. To the contrary, we show that task switching between the targets can produce an AB even without masking (Experiments 1 and 3). Further, we show that task switching produces an AB only when the second target does not belong to a class of overlearned stimuli such as letters or digits (Experiments 1 and 4). When the second target is masked, however, an AB is invariably obtained regardless of switching or overlearning. We propose that task switching involves a time-consuming process of reconfiguration of the visual system, during which the representation of the second target decays beyond recognition, resulting in an AB deficit. We suggest that overlearned stimuli are encoded in a form that, while maskable, decays relatively slowly, thus outlasting the delay due to reconfiguration and avoiding the AB deficit.