1,987 publications from this institution
This dataset includes skin conductance response (SCR) measurements for each of 22 healthy unmedicated participants (11 males and 11 females aged 24.7+/-4.5 years) participating in a visual detection task. Participants are requested to react by a keypress to a target visual stimulus (a red cross) embedded in a stream of distractors (white numbers). Stimuli are presented during 200ms and are spaced by a 800ms blank interval. A baseline period with distractors but no targets concludes the experiment. (This is in contrast to the methods description in Bach et al. (2010), according to which the baseline period was randomly either in the beginning or at the end of the experiment. This discrepancy was caused by an error in the code that controlled the experiment presentation.)
The purpose of this review was to integrate leading paradigms in psychology and neuroscience with a theory of the embodied, situated human brain, called the Hierarchically Mechanistic Mind (HMM). The HMM describes the brain as a complex adaptive system that functions to minimize the entropy of our sensory and physical states via action-perception cycles generated by hierarchical neural dynamics. First, we review the extant literature on the hierarchical structure of the brain. Next, we derive the HMM from a broader evolutionary systems theory that explains neural structure and function in terms of dynamic interactions across four nested levels of biological causation (i.e., adaptation, phylogeny, ontogeny, and mechanism). We then describe how the HMM aligns with a global brain theory in neuroscience called the free-energy principle, leveraging this theory to mathematically formulate neural dynamics across hierarchical spatiotemporal scales. We conclude by exploring the implications of the HMM for psychological inquiry.
This scientific commentary refers to ‘On the nature of seizure dynamics’, by Jirsa et al. (doi:10.1093/brain/awu133) . In this issue of Brain , Jirsa and colleagues offer a masterful account of epilepsy that discloses the universal and invariant properties of seizure dynamics (Jirsa et al. , 2014). They derive a formal taxonomy of seizure activity from the basic principles of coupled dynamical systems. In brief, they show that a minimal model—comprising just five states or variables—is sufficient to describe the onset, time-course and offset of seizure activity. This may sound implausible; however, the repertoire of dynamics that coupled systems can generate may be much smaller than people imagine. In effect, Jirsa et al. use their understanding of dynamical systems to ‘diagnose’ the mathematical aetiology of the ‘signs and symptoms’ expressed in the statistics of seizure activity. Put simply, the existence of dissociable fast discharges and spike-wave events immediately tells them that the dynamics must be generated by two pairs of (hidden) coupled states generating fast and spike-wave oscillations, respectively. The fact that seizure activity waxes and wanes over a slower timescale then calls for a further slow permittivity variable that controls the expression of fast dynamics. Within this model, the onset and offset of seizure activity become well-defined mathematical objects: a saddle node and homoclinic bifurcation, respectively. The tell-tale signatures of these bifurcations were subsequently confirmed using in vitro experiments and focal seizures recorded in humans and zebrafish. So why is this important? Without recourse to Wikipedia, I confess that I could not explain the difference between a saddle node and homoclinic bifurcation. However, this is not important: the authors have done all the mathematical heavy lifting for us and bring three things to the table: first, the notion that seizure onset (and offset) can be cast in …
The neural basis of attention to action was studied in 12 patients with Parkinson's disease (Hoehn and Yahr grades II and III) and 12 healthy age‐matched controls. The subjects were studied by functional MRI (fMRI) during performance of a simple paced overlearned motor sequence task, with and without an additional attentional task. For the attentional task, subjects were instructed to attend either to their actions or to a visual distractor task. Statistical parametric mapping was used to implement a random effects analysis of the regional task‐related activations in patient and control populations. Structural equation modelling of fMRI time series was used to measure effective connectivity among prefrontal and premotor areas. In both groups, the motor task was associated with activation of a distributed network including the premotor, motor and parietal cortex, striatum and cerebellum. In control subjects, but not patients, attention to action (relative to execution of an overlearned sequence) was associated with further activation of prefrontal, parietal and paracingulate cortex, and the supplementary motor area (SMA). Patients with Parkinson's disease showed greater than normal activation of the SMA during execution of the simple overlearned motor sequence, but less augmentation when attending to their actions. In control subjects, attention to action, but not attention to the visual distractor task, increased the effective connectivity between prefrontal cortex and both the lateral premotor cortex and the SMA. This represents a specific increase in effective connectivity. Attentional modulation of effective connectivity between the prefrontal, premotor cortex and SMA was not observed in patients. This deficit indicates a context‐specific functional disconnection between the prefrontal cortex and the supplementary and premotor cortex in Parkinson's disease.
We describe a simple and efficient solution to the problem of reconstructing electromagnetic sources into a canonical or standard anatomical space. Its simplicity rests upon incorporating subject-specific anatomy into the forward model in a way that eschews the need for cortical surface extraction. The forward model starts with a canonical cortical mesh, defined in a standard stereotactic space. The mesh is warped, in a nonlinear fashion, to match the subject's anatomy. This warping is the inverse of the transformation derived from spatial normalization of the subject's structural MRI image, using fully automated procedures that have been established for other imaging modalities. Electromagnetic lead fields are computed using the warped mesh, in conjunction with a spherical head model (which does not rely on individual anatomy). The ensuing forward model is inverted using an empirical Bayesian scheme that we have described previously in several publications. Critically, because anatomical information enters the forward model, there is no need to spatially normalize the reconstructed source activity. In other words, each source, comprising the mesh, has a predetermined and unique anatomical attribution within standard stereotactic space. This enables the pooling of data from multiple subjects and the reporting of results in stereotactic coordinates. Furthermore, it allows the graceful fusion of fMRI and MEG data within the same anatomical framework.
The superior temporal sulcus (STS) in the human and monkey is sensitive to the motion of complex forms such as facial and bodily actions. We used functional magnetic resonance imaging (fMRI) to explore network-level explanations for how the form and motion information in dynamic facial expressions might be combined in the human STS. Ventral occipitotemporal areas selective for facial form were localized in occipital and fusiform face areas (OFA and FFA), and motion sensitivity was localized in the more dorsal temporal area V5. We then tested various connectivity models that modeled communication between the ventral form and dorsal motion pathways. We show that facial form information modulated transmission of motion information from V5 to the STS, and that this face-selective modulation likely originated in OFA. This finding shows that form-selective motion sensitivity in the STS can be explained in terms of modulation of gain control on information flow in the motion pathway, and provides a substantial constraint for theories of the perception of faces and biological motion.
In this article we account for the way plants respond to salient features of their environment under the free-energy principle for biological systems. Biological self-organization amounts to the minimization of surprise over time. We posit that any self-organizing system must embody a generative model whose predictions ensure that (expected) free energy is minimized through action. Plants respond in a fast, and yet coordinated manner, to environmental contingencies. They pro-actively sample their local environment to elicit information with an adaptive value. Our main thesis is that plant behaviour takes place by way of a process (active inference) that predicts the environmental sources of sensory stimulation. This principle, we argue, endows plants with a form of perception that underwrites purposeful, anticipatory behaviour. The aim of the article is to assess the prospects of a radical predictive processing story that would follow naturally from the free-energy principle for biological systems; an approach that may ultimately bear upon our understanding of life and cognition more broadly.