Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.07.30.741910

Featural representation and internal noise around the visual field

Abstract

In human adults, visual performance varies systematically around the visual field. It is higher along the horizontal than the vertical meridian (horizontal-vertical anisotropy, HVA) and higher at the lower than the upper vertical meridian (vertical-meridian asymmetry, VMA). Although these robust performance fields have been linked to non-uniform neural resources, the system-level computations that translate neural constraints into perceptual asymmetries remain largely unexplored. Here, we used reverse correlation to characterize feature weighting and internal noise during peripheral orientation detection. Reverse correlation revealed non-ideal feature weighting in the joint orientation-spatial-frequency space, which was incorporated into a noisy-observer model jointly constrained by trial-wise detection responses and double-pass consistency. Across observers, the magnitude of the HVA in contrast sensitivity was correlated with individual asymmetries in orientation sensitivity and additive internal noise. In contrast, we found limited evidence that any tested representational or noise components reliably accounted for individual differences in VMA magnitude. Spatial-frequency tuning exhibited substantial individual variability, often peaking below the signals spatial frequency, but did not vary systematically across locations or explain performance asymmetries. These findings suggest that the HVA reflects systematic variation in the feature weighting of task-relevant orientations and internal noise, while constraining which computational components provide robust explanations of polar-angle asymmetries. Moreover, our framework provides a principled approach that links this prevalent perceptual asymmetry to the system-level computations that transform sensory information into perceptual decisions. Author summaryHuman vision is surprisingly uneven across our field of view. At the same distance from where we look, vision is better along the horizontal axis than the vertical axis, and better in the lower than the upper half of the vertical axis. These differences are well established, but little is known about their computational basis. To investigate, we combined visual detection tasks with computational modeling. By analyzing how observers detected faint patterns within noisy images, we measured how they process distinct features--like patterns with different orientations and spatial frequencies at different visual field locations. We then fit a mathematical model to separate distinct sources of internal noise. We found that differences in how the brain processes line orientations predicted the magnitude of the horizontal-vertical asymmetry across individuals, whereas distinct components of internal noise predicted these asymmetries in different ways. Our results show that visual field asymmetries are not driven by a single visual bottleneck, but rather by location-specific combinations of how the brain encodes relevant feature information and neural noise. This study helps explain why human vision is fundamentally uneven across our field of view.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Xue, S., Landy, M., Carrasco, M.. 2026-08-05. Featural representation and internal noise around the visual field. https://doi.org/10.64898/2026.07.30.741910

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

KEEP EXPLORING

Related preprints

Functional validation of allele-specific LMNB1 silencing in patient-derived astrocytes as a therapeutic option for Autosomal Dominant Leukodystrophy

Adult-onset Autosomal Dominant Leukodystrophy (ADLD) is a rare fatal leukodystrophy caused by increased LMNB1 gene dosage, most commonly resulting from duplication of the LMNB1 locus. Because ADLD is a gene dosage disorder, selective reduction of pathological LMNB1 expression represents a rational therapeutic strategy. Although allele-specific RNA interference has previously been shown to lower LMNB1 levels in patient-derived fibroblasts and directly reprogrammed neurons, its therapeutic effects have not been evaluated in disease-relevant human glial cells or using functional efficacy endpoints. Here, we established human induced pluripotent stem cell-derived astrocytes from ADLD patients as a human glial model in which to validate allele-specific LMNB1 silencing across molecular, cellular, and functional readouts. ADLD astrocytes recapitulated increased LMNB1 expression and characteristic nuclear abnormalities and displayed transcriptional alterations affecting extracellular matrix organization, calcium homeostasis, metabolism and RNA processing. Functionally, these cells also exhibited functional phenotypes suitable for therapeutic evaluation: astrocyte-conditioned medium impaired the viability of both murine and human oligodendroglial cultures, while conditioned-medium and direct astrocyte-seeding paradigms revealed impaired post-lesion myelin recovery in lysolecithin-treated cerebellar organotypic slices. Allele-specific LMNB1 silencing restored physiological LMNB1 levels, corrected nuclear abnormalities, attenuated astrocyte-mediated oligodendroglial toxicity, improved post-lesion myelin recovery, and was associated with selective transcriptional programs associated with extracellular support and cholesterol metabolism. Together, these findings provide molecular, cellular, and functional validation of allele-specific LMNB1 dosage correction in patient-derived human astrocytes and offer key support for LMNB1-lowering strategies in disease-relevant human glial cells.

neuroscience↗

Perceptual integration of multisensory haptic, visual, and auditory feedback for roughness discrimination in augmented reality

Understanding how our different senses interact to shape our perception is essential to design realistic and immersive virtual and augmented reality (VR/AR) experiences. The present study investigated how roughness perception can be modulated through haptic, visual, and auditory cues in AR using a vibrotactile wristband. Participants compared virtual textures varying in vibration frequency/amplitude, visual grain size, and friction sound. Results revealed strong linear relationships between stimulus parameters and perceived roughness, with haptic frequency and visual cues driving the highest discrimination performance. Adding non-informative sensory feedback reduced perceptual sensitivity, acting as noise. Individual differences emerged: participants who rated haptic as the easiest modality showed greater sensitivity to haptic variations, while visual-reliant participants performed better with visual cues. We conclude that roughness in AR can be systematically manipulated, but is vulnerable to perceptual interference from irrelevant inputs, where our work provides actionable insights for implementing optimized and adaptive AR/VR interfaces.

neuroscience↗

Structural and functional MRI signatures of Gambling Disorder: a case-control study

Gambling disorder (GD) is a behavioural addiction that may help identify addiction-related neural features without the direct neurobiological effects of a primary substance of dependence. We examined regional grey matter volume (GMV) and resting-state functional connectivity (rsFC) in the same well-characterised sample. Eighteen men with GD and 21 matched healthy controls underwent high-resolution structural and resting-state functional MRI. GMV was quantified across 214 cortical and subcortical regions, and seed-based rsFC analyses focused on striatal subdivisions and mesocorticolimbic regions. Group differences were evaluated using permutation testing and cluster-corrected mixed-effects modelling. GD was associated with lower GMV in the ventromedial prefrontal cortex, orbitofrontal regions and other cortical and subcortical areas, alongside higher GMV in a subset of limbic and default-mode regions. Participants with GD also showed lower connectivity between the limbic striatum and the hippocampus, thalamus and putamen. In exploratory analyses, somatomotor connectivity was positively associated with gambling severity (Problem Gambling Severity Index: Spearman's rho = 0.71, p = 0.003, false-discovery-rate-adjusted q = 0.016). Structural and functional findings overlapped spatially in regions associated with valuation, memory, reward and habit formation, but regional GMV did not mediate group differences in rsFC. These findings are broadly consistent with corticostriatal models of GD and identify candidate circuit-level differences for independent replication. Larger, more diverse and longitudinal samples are required to establish their reproducibility, temporal direction and clinical relevance.

neuroscience↗