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Volz, L. J.

Publications and source records attributed to Volz, L. J..

3 recordsLinked to original sources

Motor learning adapts to effort-dependent uncertainty

Adaptive behaviour depends on continuously updating motor control when action outcomes differ from expectations. Because action execution and sensory feedback are noisy, the value of an error depends on how reliably it reflects the consequences of an action. Most studies have manipulated the reliability of sensory feedback or action outcomes rather than uncertainty generated by the action itself. Here we show that motor adaptation is calibrated to effort-dependent uncertainty arising during action generation. Using a force-based motor adaptation paradigm, we demonstrate that greater effort progressively increased uncertainty in action execution and proprioceptive feedback, with corresponding changes in adaptation rate that closely matched normative predictions. Reward enhanced adaptation by improving proprioceptive precision rather than directly changing adaptation rate. Supporting this framework, patients with major depressive disorder exhibited elevated execution and proprioceptive uncertainty, impaired reward-dependent improvement in proprioceptive precision, and slower motor adaptation. These findings establish intrinsic uncertainty as a general determinant of adaptive behaviour, linking action generation, sensory evaluation, and motivation.

neuroscience↗

No Disconnection Syndrome after Near-Complete Callosotomy

Sensorimotor processing in the human brain is largely lateralized, with the corpus callosum integrating these processes into a unified experience. Following complete callosotomy, this integration breaks down, resulting in disconnection syndromes. We asked how much of the corpus callosum is sufficient to support functional unity--the absence of disconnection syndrome--by comparing three complete callosotomy patients with one retaining only the splenium. Using lateralized tasks across visual, tactile, visuospatial, and language domains, we predicted domain-specific deficits in the splenium-only patient based on established anatomical models of callosal topography. Strikingly, while complete callosotomy patients exhibited disconnection syndromes, the splenium patient demonstrated functional unity across all domains--as if his entire corpus callosum were intact. Our findings highlight the brains remarkable capacity to maintain behavioral integration through minimal preserved pathways, highlighting how the structure-dependent reorganizational capacity of the human brain allows to preserve functional unity.

neuroscience↗

Full inter-hemispheric integration sustained by a fraction of posterior callosal fibers

The dynamic integration of the lateralized and specialized capacities of the cerebral hemispheres constitutes a hallmark feature of human brain function. This inter-hemispheric exchange of information critically depends upon the corpus callosum. Classical descriptions of callosal organization outline a topographic gradient, such that specific fibers integrate distinct aspects of brain function. Here we present a challenge to this conventional model. Using neuroimaging data obtained from a new cohort of adult corpus callosotomy patients, we leverage modern network neuroscience techniques to show--for the first time--that full inter-hemispheric integration can be achieved via a small proportion ([~]1 cm) of intact posterior callosal fibers. Only complete callosotomy patients demonstrated the expected dissolution of typical inter-hemispheric network architectures, aligning with disconnection syndromes long-thought to reflect diminished information propagation and communication across the brain. These findings motivate a novel mechanistic understanding of synchronized inter-hemispheric neural activity for large-scale human brain function and behavior.

neuroscience↗