Evidence map›Paper›PMID 41273265›Full record

ArticleDevelopmental science2026

Computationally Probing the Role of Time-Limited Neuronal Plasticity in Early Visual Development.

Marin Vogelsang, Lukas Vogelsang, Pawan Sinha

Abstract read
In one paragraph

Article in Developmental science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Marin VogelsangDepartment of Brain and Cognitive Sciences, MIT, Cambridge, Massachusetts, USA.
Lukas VogelsangDepartment of Brain and Cognitive Sciences, MIT, Cambridge, Massachusetts, USA.
Pawan SinhaDepartment of Brain and Cognitive Sciences, MIT, Cambridge, Massachusetts, USA.

Funding

Project Prakash: Development of Object Perception After Late Sight OnsetR01EY020517 · NEI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SINHA, PAWAN · 2011 to 2025
$8.9M
Japan Society for the Promotion of ScienceNEI NIH HHS R01 EY020517NEI NIH HHS R01EY020517Simons Center for the Social BrainSimons Foundation InternationalYamada Science Foundation
6 · The paper itself

Abstract

In the first months or years of life, newborns learn to perceive their environment at a remarkable pace. This capacity is often attributed to heightened neuronal plasticity that diminishes over time. While this decline in plasticity could be seen as constituting a mere biological constraint, we ask whether it might, in fact, serve an adaptive function. A natural consequence of time-limited plasticity is the preservation of sensory processing mechanisms formed early in life. Emerging evidence has supported the "adaptive initial degradation" hypothesis, which posits that early experience with degraded sensory inputs, such as blurred or color-reduced vision, helps instantiate important sensory mechanisms subserving robust perception later in life. Here, we employ deep neural networks as computational models to systematically probe how developmental improvements in visual fidelity interact with diminishing plasticity, modeled via decreasing learning rates. Across both acuity and color domains, we find that time-limited plasticity yields modest performance gains and helps stabilize early-formed representations. However, these improvements remain surprisingly modest. Further analysis of the networks' internal representations also reveals that earlier layers stabilize sooner than deeper layers, loosely paralleling findings from biological development. Overall, our results suggest that while declining plasticity can confer small benefits, it is not the primary force behind the more pronounced advantages of commencing visual experience with degraded inputs. These insights refine the "adaptive initial degradation" hypothesis and, more broadly, underscore how computational modeling can shed light on longstanding questions in developmental neuroscience. SUMMARY: Time-limited neuronal plasticity is often viewed as a mere biological constraint. However, might it provide adaptive advantages by preserving sensory mechanisms learned early in development? Simulations with initially degraded sensory inputs reveal modest performance gains when modeling time-limited plasticity as decreasing learning rates. Despite these gains, plasticity reductions contribute less than the benefits conferred by starting with degraded inputs, refining the "adaptive initial degradation" hypothesis. These results underscore the utility of computational models to illuminate questions in developmental neuroscience and point to interesting future research avenues.

Indexed as

Neuronal PlasticityVisual PerceptionComputer SimulationHumansLearningModels, NeurologicalNeural Networks, ComputerTime Factorsacuityadaptive initial degradationscolordeep neural networksperceptual developmentvisual development

Identifiers

PMID41273265
PMCPMC12640114

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.