bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.04.03.646752

Temporal adaptation aids object recognition in deep convolutional neural networks in suboptimal viewing scenario's

Abstract

The primate visual system excels in recognizing objects under challenging viewing scenarios. A neural mechanism that is thought to play a key role in this ability is rapid temporal adaptation, or the adjustment of neurons activity based on recent history. To understand how temporal adaptation may support object recognition, previous work has incorporated a variety of temporal feedback mechanisms in deep convolutional neural networks (DCNN) and explored how these mechanisms affect object recognition performance. While multiple adaptation mechanisms have been shown to impact model behavior, it remains unclear how the origin (intrinsic or recurrent) and the way the temporal feedback is integrated (additive or multiplicative) affects object recognition. Here, we compare the impact of four different temporal adaptation mechanisms on object recognition using three different task designs, including object recognition under either noise or occlusion, and in the context of novelty detection. Our results show that the effectiveness of temporal adaptation mechanisms for robust object recognition depends on the task and dataset. For objects embedded in noise, intrinsic adaptation excels with simple, high-contrast inputs, while recurrent mechanisms perform better with complex, low-contrast inputs, highlighting their focus on different visual features. Under dynamic occlusion, recurrent adaptation mechanisms exhibit a more progressive increase in performance over time, suggesting they better maintain object coherence when parts are obscured. For novelty detection, recurrent mechanisms show higher performance compared to intrinsic adaptation mechanisms, suggesting that recurrence aids in detecting global changes caused by the presentation of new objects. All together, these findings suggest that robust object recognition likely requires multiple temporal adaptation strategies in parallel to handle the diverse challenges of naturalistic visual settings.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Brands, A. M., Lange, G., Groen, I. I. A.. 2025-04-03. Temporal adaptation aids object recognition in deep convolutional neural networks in suboptimal viewing scenario's. https://doi.org/10.1101/2025.04.03.646752

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↗