Locality and weight sharing shape Hebbian principal-component learning in biologically constrained visual models.

IF 3.3 4区 医学 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Frontiers in Computational Neuroscience Pub Date : 2026-09-21 eCollection Date: 2026-01-01 DOI:10.3389/fncom.2026.1943064
Patrick Inoue, Florian Röhrbein, Andreas Knoblauch
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引用次数: 0

Abstract

Introduction: Biologically motivated artificial visual learning requires local plasticity rules to be evaluated within architectures whose connectivity assumptions remain explicit. Convolutional Hebbian networks demonstrate that competitive local learning can support visual classification, but their performance is coupled to exact weight sharing, a prior that is not anatomically literal. This study asks whether Hebbian principal component analysis (HPCA) can support representations when spatial locality is preserved but exact translational weight sharing is removed.

Methods: HPCA was evaluated on CIFAR-10 as the primary benchmark, with MNIST and STL-10 used as controls. We compared fully connected HPCA, position-specific locally connected HPCA with fixed receptive fields, non-shared synaptic weights, and population-wise divisive response normalization, and HPCA substitutions in two shared-kernel convolutional Hebbian benchmarks. Representations were learned without supervised feature-layer targets or BP-based feature-layer fine-tuning, frozen, and evaluated through supervised readouts.

Results: Position-specific locally connected HPCA outperformed the fully connected reference. On CIFAR-10, the best locally connected model reached 61.42 ± 0.36%. Shared-kernel HPCA reached 74.51 ± 0.38% in the modular benchmark with common HPCA preprocessing and 76.57 ± 0.55% in the SoftHebb architecture with reference preprocessing.

Discussion: The results show that HPCA remains effective across position-specific locally connected and shared-kernel convolutional architectures, but that performance depends strongly on the surrounding architecture and benchmark protocol. The tested shared-kernel configurations achieved higher accuracy, yet useful frozen visual representations still emerged when exact parameter sharing was removed. Locally connected HPCA therefore provides a controlled model for examining how local plasticity interacts with receptive-field structure and convolutional inductive bias in biologically constrained visual learning.

局部性和权值共享形成了生物约束视觉模型中的Hebbian主成分学习。
生物驱动的人工视觉学习需要在连通性假设仍然明确的架构中评估局部可塑性规则。卷积Hebbian网络证明了竞争的局部学习可以支持视觉分类,但它们的性能与精确的权重共享相关联,这是一个不符合解剖学字面意义的先验。本研究询问Hebbian主成分分析(HPCA)是否可以支持表征时,空间局部性是保留的,但确切的平移权共享被删除。方法:以CIFAR-10为主要基准,以MNIST和STL-10为对照,进行HPCA评价。在两个共享核卷积Hebbian基准中,我们比较了完全连接的HPCA、具有固定接受野、非共享突触权重和种群分裂响应归一化的位置特异性局部连接HPCA以及HPCA替换。表征是在没有监督特征层目标或基于bp的特征层微调的情况下学习的,通过监督读出进行冻结和评估。结果:特定位置局部连接的HPCA优于完全连接的参考。在CIFAR-10上,最佳局部连接模型达到61.42±0.36%。共享内核HPCA在采用通用HPCA预处理的模块化基准测试中达到74.51±0.38%,在采用参考预处理的SoftHebb架构中达到76.57±0.55%。讨论:结果表明,HPCA在特定位置的局部连接和共享内核卷积架构中仍然有效,但性能在很大程度上取决于周围的架构和基准协议。经过测试的共享内核配置获得了更高的准确性,但是当移除精确的参数共享时,仍然会出现有用的冻结视觉表示。因此,局部连接的HPCA提供了一个受控模型,用于研究局部可塑性如何与生物受限视觉学习中的接受场结构和卷积归纳偏差相互作用。
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来源期刊
Frontiers in Computational Neuroscience
Frontiers in Computational Neuroscience MATHEMATICAL & COMPUTATIONAL BIOLOGY-NEUROSCIENCES
CiteScore
5.30
自引率
3.10%
发文量
166
审稿时长
6-12 weeks
期刊介绍: Frontiers in Computational Neuroscience is a first-tier electronic journal devoted to promoting theoretical modeling of brain function and fostering interdisciplinary interactions between theoretical and experimental neuroscience. Progress in understanding the amazing capabilities of the brain is still limited, and we believe that it will only come with deep theoretical thinking and mutually stimulating cooperation between different disciplines and approaches. We therefore invite original contributions on a wide range of topics that present the fruits of such cooperation, or provide stimuli for future alliances. We aim to provide an interactive forum for cutting-edge theoretical studies of the nervous system, and for promulgating the best theoretical research to the broader neuroscience community. Models of all styles and at all levels are welcome, from biophysically motivated realistic simulations of neurons and synapses to high-level abstract models of inference and decision making. While the journal is primarily focused on theoretically based and driven research, we welcome experimental studies that validate and test theoretical conclusions. Also: comp neuro
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