Peripersonal space (PPS) as a primary interface for self-environment interactions
Peripersonal space (PPS) defines the portion of space where interactions between our body and the external environment more likely occur. There is no physical boundary defining the PPS with respect to the extrapersonal space, but PPS is continuously constructed by a dedicated neural system integrating external stimuli and tactile stimuli on the body, as a function of their potential interaction. This mechanism represents a primary interface between the individual and the environment. In this talk, I will present most recent evidence and highlight the current debate about the neural and computational mechanisms of PPS, its main functions and properties. I will discuss novel data showing how PPS dynamically shapes to optimize body-environment interactions. I will describe a novel electrophysiological paradigm to study and measure PPS, and show how this has been used to search for a basic marker of potentials of self-environment interaction in newborns and patients with disorders of consciousness. Finally, I will discuss how PPS is also involved in, and in turn shaped by, social interactions. Under these acceptances, I will discuss how PPS plays a key role in self-consciousness.
Neural Codes for Natural Behaviors in Flying Bats
This talk will focus on the importance of using natural behaviors in neuroscience research – the “Natural Neuroscience” approach. I will illustrate this point by describing studies of neural codes for spatial behaviors and social behaviors, in flying bats – using wireless neurophysiology methods that we developed – and will highlight new neuronal representations that we discovered in animals navigating through 3D spaces, or in very large-scale environments, or engaged in social interactions. In particular, I will discuss: (1) A multi-scale neural code for very large environments, which we discovered in bats flying in a 200-meter long tunnel. This new type of neural code is fundamentally different from spatial codes reported in small environments – and we show theoretically that it is superior for representing very large spaces. (2) Rapid modulation of position × distance coding in the hippocampus during collision-avoidance behavior between two flying bats. This result provides a dramatic illustration of the extreme dynamism of the neural code. (3) Local-but-not-global order in 3D grid cells – a surprising experimental finding, which can be explained by a simple physics-inspired model, which successfully describes both 3D and 2D grids. These results strongly argue against many of the classical, geometrically-based models of grid cells. (4) I will also briefly describe new results on the social representation of other individuals in the hippocampus, in a highly social multi-animal setting. The lecture will propose that neuroscience experiments – in bats, rodents, monkeys or humans – should be conducted under evermore naturalistic conditions.
Scaffolding up from Social Interactions: A proposal of how social interactions might shape learning across development
Social learning and analogical reasoning both provide exponential opportunities for learning. These skills have largely been studied independently, but my future research asks how combining skills across previously independent domains could add up to more than the sum of their parts. Analogical reasoning allows individuals to transfer learning between contexts and opens up infinite opportunities for innovation and knowledge creation. Its origins and development, so far, have largely been studied in purely cognitive domains. Constraining analogical development to non-social domains may mistakenly lead researchers to overlook its early roots and limit ideas about its potential scope. Building a bridge between social learning and analogy could facilitate identification of the origins of analogical reasoning and broaden its far-reaching potential. In this talk, I propose that the early emergence of social learning, its saliency, and its meaningful context for young children provides a springboard for learning. In addition to providing a strong foundation for early analogical reasoning, the social domain provides an avenue for scaling up analogies in order to learn to learn from others via increasingly complex and broad routes.
The role of orexin/hypocretin in social behaviour
My lab is focused on how brain encodes and modulates social interactions. Intraspecific social interactions are integral for survival and maintenance of society among all mammalian species. Despite the importance of social interactions, we lack a complete understanding of the brain circuitry involved in processing social behaviour. My lab investigates how the hypothalamic orexin (hypocretin) neurons and their downstream circuits participate in social interaction behaviours. These neurons are located exclusively in the hypothalamus that regulates complex and goal-directed behaviours. We recently identified that orexin neurons differentially encode interaction between familiar and novel animals. We are currently investigating how chronic social isolation, a risk factor for the development of social-anxiety like behaviours, affects orexin neuron activity and how we can manipulate the activity of these neurons to mitigate isolation-induced social deficits.
Neural and computational principles of the processing of dynamic faces and bodies
Body motion is a fundamental signal of social communication. This includes facial as well as full-body movements. Combining advanced methods from computer animation with motion capture in humans and monkeys, we synthesized highly-realistic monkey avatar models. Our face avatar is perceived by monkeys as almost equivalent to a real animal, and does not induce an ‘uncanny valley effect’, unlike all other previously used avatar models in studies with monkeys. Applying machine-learning methods for the control of motion style, we were able to investigate how species-specific shape and dynamic cues influence the perception of human and monkey facial expressions. Human observers showed very fast learning of monkey expressions, and a perceptual encoding of expression dynamics that was largely independent of facial shape. This result is in line with the fact that facial shape evolved faster than the neuromuscular control in primate phylogenesis. At the same time, it challenges popular neural network models of the recognition of dynamic faces that assume a joint encoding of facial shape and dynamics. We propose an alternative physiologically-inspired neural model that realizes such an orthogonal encoding of facial shape and expression from video sequences. As second example, we investigated the perception of social interactions from abstract stimuli, similar to the ones by Heider & Simmel (1944), and also from more realistic stimuli. We developed and validated a new generative model for the synthesis of such social interaction, which is based on a modification of human navigation model. We demonstrate that the recognition of such stimuli, including the perception of agency, can be accounted for by a relatively elementary physiologically-inspired hierarchical neural recognition model, that does not require the assumption of sophisticated inference mechanisms, as postulated by some cognitive theories of social recognition. Summarizing, this suggests that essential phenomena in social cognition might be accounted for by a small set of simple neural principles that can be easily implemented by cortical circuits. The developed technologies for stimulus control form the basis of electrophysiological studies that can verify specific neural circuits, as the ones proposed by our theoretical models.