bioRxiv Science⌕ Search

bioRxiv · 10.1101/2022.07.12.499675

"Leap before you look": Conditions that promote implicit visuomotor adaptation without explicit learning

Abstract

When learning a novel visuomotor mapping (e.g., mirror writing), accuracy can improve quickly through explicit learning (e.g., move left to go right) but after considerable practice, implicit learning takes over, producing fast, natural movements. This implicit learning occurs automatically, but it has been unknown whether explicit learning is similarly obligatory. Using a reaching task with a 90-degree rotation between screen position and movement direction, we found that explicit learning could be "turned off" by introducing the rotation gradually (increments of 10-degrees) and instructing participants to move quickly. These specific conditions were crucial, because both explicit and implicit learning occurred if the rotation occurred suddenly, if participants were told to emphasize accuracy, or if visual feedback during movement was removed. We reached these conclusions by examining the time course of learning (e.g., whether there was fast improvement followed by a long tail of additional improvement), by examining the aftereffects of learning when the rotation was abruptly removed, and by using formal model comparison between a dual-state (explicit and implicit) versus a single-state learning model as applied to the data. Author summaryIn some situations, the relationship between motion direction and what we see is different than normal. For instance, try using a computer mouse that is held sideways (a 90-degree rotation). When first encountering this situation, people move carefully, using explicit strategies (e.g., move right to go up). However, after many learning trials, motion becomes automatic (implicit) and natural. Prior results found that implicit visuomotor learning always occurs with enough experience. In our study, we found that this is not true of explicit visuomotor learning; in some situations, explicit learning can be turned off. More specifically, we found that this occurs when the novel visuomotor situation is: 1) introduced gradually (e.g., a gradual introduction of 90-degree rotation in steps of 10 degrees); 2) when there is pressure to move quickly; and 3) with real-time onscreen views of the motion path. If any of these three components are missing, then people use explicit learning. These conclusions were reached by examining the time course of learning (e.g., whether there was both fast and slow learning as assessed with mathematical models) and by examining the tendency to automatically move in the opposite direction from the rotation when the rotation is abruptly removed after learning.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Savalia, T., Cowell, R., Huber, D.. 2022-07-13. "Leap before you look": Conditions that promote implicit visuomotor adaptation without explicit learning. https://doi.org/10.1101/2022.07.12.499675

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

The Unreasonable Effectiveness of Cell Types in Describing Neuronal Physiological Features

Single-cell RNA sequencing (scRNA-seq) captures detailed gene expression profiles at scale, while patch-clamp recordings measure intrinsic neuronal electrophysiological properties. Modeling the relations between these two modalities remains a challenge. Here, we compare how well electrophysiological features can be predicted by traditional transcriptomic cell type classification, representations derived from a foundational model (scGPT) pretrained on large-scale scRNA-seq datasets, ion channel-coding genes, and highly variable genes. Using paired transcriptomic and electrophysiological patch-sequencing data from 495 human neurons from neurosurgical tissue, we find that cluster-level cell type representations consistently outperform highly variable gene selection, ion channel gene selection, and context-enriched scGPT embeddings. Notably, performance varies across model architectures and initializations, and the best results are obtained by combining the outputs of separate cell type and scGPT-based models. Together, these findings suggest that traditional discrete cellular classification is highly effective in predicting physiological features. For maximum performance it can be complemented by pretrained transformer models.

neuroscience↗

A nonlinear inhibition pathway underlying cortical responses to tuned holographic optogenetic perturbations

Optogenetics enables causal manipulation of cortical activity. Perturbation responses can be counterintuitive due to network interactions, making theory essential for predicting them. Existing approaches often rely on linear approximations, which fail for many biologically relevant perturbations. Here we develop a nonlinear theory of responses to holographic perturbations in cell-type-specific recurrent networks with structured connectivity. We fit a nonlinear model to mouse V1 data, which shows cotuned-ensemble suppression: perturbing spatially clustered neurons with similar preferred orientations yields markedly stronger short-range suppression than perturbing untuned ensembles. We show that cotuned-ensemble suppression arises from a feature-tuned, nonlinear inhibition pathway implicating somatostatin-positive (SST) interneurons. The theory predicts that cotuned ensembles suppress parvalbumin-positive (PV) neurons but facilitate SST neurons, and links the degree of cotuned-ensemble suppression or facilitation to the variance of the SST response. This framework identifies mechanisms by which nonlinear inhibition sculpts cortical dynamics and establishes a predictive basis for targeted optogenetic interventions.

neuroscience↗

Proteomic signatures of APOE ε4 across human tissues and cell types in Alzheimers disease

The apolipoprotein E {varepsilon}4 (APOE {varepsilon}4) allele is the strongest genetic risk factor for late-onset Alzheimers disease (AD). However, the underlying molecular mechanisms remain unclear. This study included 1691 participants from the Religious Orders Study and Rush Memory and Aging Project (ROSMAP), 1226 participants from the Accelerating Medicines Partnership - Alzheimers Disease (AMP-AD) Diverse Cohorts Study, and 735 participants from the Alzheimers Disease Neuroimaging Initiative (ADNI). To characterise APOE {varepsilon}4 molecular effects, we analysed proteomic data from plasma, cerebrospinal fluid (CSF), and induced pluripotent stem cell (iPSC)-derived astrocytes and neurons, as well as transcriptomic and proteomic data from multiple brain regions. The association of APOE {varepsilon}4 with AD neuropathology was also examined. APOE {varepsilon}4 carriers shared a plasma proteomic signature enriched for immune processes, irrespective of AD diagnosis. A machine learning classifier trained on this signature discriminated APOE {varepsilon}4 carriers from non-carriers in an independent cohort using CSF proteomics. APOE {varepsilon}4 carriage was associated with higher Braak stages and Consortium to Establish a Registry for Alzheimers Disease (CERAD) score. However, only limited APOE {varepsilon}4-associated transcriptomic and proteomic changes were observed in bulk brain tissue, with poor cross-layer concordance. Proteomic analyses of iPSC-derived astrocytes and neurons further revealed cell-type-specific APOE {varepsilon}4-associated changes. APOE {varepsilon}4 is associated with a consistent proteomic signature across plasma and CSF. Its molecular effects in the brain differ across cell types, brain regions and molecular layers. These findings support the need for cell-type-resolved multi-omic studies to elucidate how APOE {varepsilon}4 confers AD risk.

neuroscience↗