# Dimensionality reduction techniques in pupillometry research: A primer for behavioral scientists

**Authors:** Serena Castellotti, Irene Petrizzo, Roberto Arrighi, Elvio Blini

PMC · DOI: 10.3758/s13428-025-02786-0 · Behavior Research Methods · 2025-11-10

## TL;DR

This paper introduces a new analytical approach for pupillometry data using dimensionality reduction to uncover underlying physiological processes.

## Contribution

The paper proposes using temporal principal components analysis to recover latent physiological processes in pupillometry data.

## Key findings

- Dimensionality reduction reveals a low-dimensional space representing core physiological processes in pupil size changes.
- The pupillary manifold provides a more efficient and physiology-aware analytical framework.
- The R library 'Pupilla' offers tools for implementing these techniques.

## Abstract

The measurement of pupil size is a classic tool in psychophysiology, but its popularity has recently surged due to the rapid developments of the eye-tracking industry. Concurrently, several authors have outlined a wealth of strategies for tackling pupillary recordings analytically. The consensus is that the “temporal” aspect of changes in pupil size is key, and that the analytical approach should be mindful of the temporal factor. Here we take a more radical stance on the matter by suggesting that, by the time significant changes in pupil size are detected, it is already too late. We suggest that these changes are indeed the result of distinct, core physiological processes that originate several hundreds of milliseconds before that moment and altogether shape the observed signal. These processes can be recovered indirectly by leveraging dimensionality reduction techniques. Here we therefore outline key concepts of temporal principal components analysis and related rotations to show that they reveal a latent, low-dimensional space that represents these processes very efficiently: a pupillary manifold. We elaborate on why assessing the pupillary manifold provides an alternative, appealing analytical solution for data analysis. In particular, dimensionality reduction returns scores that are (1) mindful of the relevant physiology underlying the observed changes in pupil size, (2) extremely handy and manageable for statistical modelling, and (3) devoid of several arbitrary choices. We elaborate on these points in the form of a tutorial paper for the functions provided in the accompanying R library “Pupilla.”

## Full-text entities

- **Genes:** PCSK1 (proprotein convertase subtilisin/kexin type 1) [NCBI Gene 5122] {aka BMIQ12, NEC1, PC1, PC1/3, PC3, SPC3}
- **Diseases:** PCA (MESH:C566443), WML (MESH:C536761), stroke (MESH:D020521), anxiety (MESH:D001007), Pupil dilation (MESH:D011681), deficit (MESH:D009461)
- **Chemicals:** noradrenaline (MESH:D009638)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12602682/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12602682/full.md

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Source: https://tomesphere.com/paper/PMC12602682