The Science of Consciousness 2026 · San Diego, CA
Poster Session 1 · Tuesday, 13 October 2026 · 7:30 pm
The Internal Dynamics of Decisions: From rats and primates to AI
Nathan M. Thornhill· ORCID 0009-0009-3161-528X
Institute for Complexity Science and Advanced Computing (ICSAC), Fort Wayne, Indiana
Brain or AI model?Round 1 of 8
A
B
Which one is the brain?
Schematic phase portraits, drawn in neutral until you answer. What is measured,
and what sets how far each one wanders, is the share of the next state that arrives from
outside rather than from the population itself.
For thirty years the argument has been whether it matters how a system computes
or only what it computes. The usual objection is that behaviour can never answer it, since a
feedforward network can copy any brain’s behaviour. Six networks wired two ways, trained
to the same score on one task, and their dynamics still tell them apart.
The axis
Opposite regimes
Brains run on themselves (recurrence).
AI models run on what you feed them (input). Rat and monkey were
recorded in different brain areas, doing unrelated jobs.
Brain
75 of 115
Sessions
The rat decides. Then its cortex tightens its grip.
Luo et al. 2025, 115 sessions from 12 rats, about 36,000 frontal and striatal
units. Recovered, not discovered here. These are separate recordings from the rat cortex you
play against, which is Schiereck et al. 2026.
AI model
0 of 54
Depth tests
The AI model decides. Nothing tightens. Then it runs out of layers.
Both models tested commit at the final layer, so nothing comes after it to
settle.
How. A subspace state-space demix splits each next state into input drive
and the population’s own recurrence, validated on synthetic systems with known answers
before any real data. The six architectures were matched on size as well as score, and
none of the 144 networks was dropped, so the signature tracks architecture, not task.
The estimator is N4SID (Van Overschee & De Moor 1994) and the input-aware demix is InputDSA
(Huang et al. 2025), on Ostrow et al. 2023.
What this does not show. No claim about phenomenal experience or
machine sentience. What is measured is decision commitment, which is not conscious access.
That gap is the central limitation.
Bio
Nathan M. Thornhill is a complexity science researcher in Fort Wayne, Indiana,
working in information theory and pattern persistence. He is self-taught, and his earlier career
was in healthcare: nursing assistant, then nursing-home administration, then ICU admissions.
What he studies is whether a system holds together and how you would measure that: pattern
persistence in simple discrete systems, sleep stages from EEG, task success read off a
model’s internal geometry. The analysis plans get written down and frozen first, and the
measures that fail are reported next to the ones that work. The results so far are out as
preprints and one book.
When he isn’t researching he’s playing guitar, gardening, or with his wife and
daughter.
How this work gets madeWho pays for it
No university and no grant. A web design business pays for the research, ICSAC publishes it,
and two of the tools the research needed have since turned into products that bring in money of
their own.
Every recording analysed here is public and was collected by other laboratories. Nothing
on this poster required new animal work.
Luo TZ et al. 2025. Data from: Transitions in dynamical regime and neural mode during perceptual decisions. Dryad. doi:10.5061/dryad.sj3tx96dm
Neupane S, Fiete I, Jazayeri M. 2024. Mental navigation in the primate entorhinal cortex. DANDI Archive, dandiset 000897. dandiarchive.org/dandiset/000897
Schiereck SS et al. 2026. Data from: The orbitofrontal cortex updates beliefs for state inference. Zenodo. doi:10.5281/zenodo.16997337
Pre-registrations. Both analysis plans were written down and frozen before a single
dynamical measure was computed, and both are carried in the preprint:
doi.org/10.20944/preprints202608.1095.v1. The measure that separates the six
networks and the one that does not were both named in advance, and both are reported.
References
The sources the poster draws on. The preprint carries the full text and both
pre-registrations.
Show allHide18 references
Belrose N, Ostrovsky I, McKinney L, Furman Z, Smith L, Halawi D, Biderman S, Steinhardt J. 2023. Eliciting latent predictions from transformers with the tuned lens. arXiv:2303.08112
Block N. 1995. On a confusion about a function of consciousness. Behavioral and Brain Sciences 18(2):227–247. doi:10.1017/S0140525X00038188
Doerig A, Schurger A, Hess K, Herzog MH. 2019. The unfolding argument: why IIT and other causal structure theories cannot explain consciousness. Consciousness and Cognition 72:49–59. doi:10.1016/j.concog.2019.04.002
Doerig A, Schurger A, Herzog MH. 2021. Hard criteria for empirical theories of consciousness. Cognitive Neuroscience 12(2):41–62. doi:10.1080/17588928.2020.1772214
Huang A, Ostrow M, Singh SH, Kozachkov L, Fiete I, Rajan K. 2025. InputDSA: demixing then comparing recurrent and externally driven dynamics. ICLR 2026. arXiv:2510.25943
Kleiner J, Hoel E. 2021. Falsification and consciousness. Neuroscience of Consciousness 2021(1):niab001. doi:10.1093/nc/niab001
Lamme VAF. 2006. Towards a true neural stance on consciousness. Trends in Cognitive Sciences 10(11):494–501. doi:10.1016/j.tics.2006.09.001
Luo TZ, Kim TD, Gupta D, Bondy AG, Kopec CD, Elliott VA, DePasquale B, Brody CD. 2025. Transitions in dynamical regime and neural mode during perceptual decisions. Nature 646(8087):1156–1166. doi:10.1038/s41586-025-09578-8
[dataset] Luo TZ et al. 2025. Data from: Transitions in dynamical regime and neural mode during perceptual decisions. Dryad. doi:10.5061/dryad.sj3tx96dm
Mante V, Sussillo D, Shenoy KV, Newsome WT. 2013. Context-dependent computation by recurrent dynamics in prefrontal cortex. Nature 503(7474):78–84. doi:10.1038/nature12742
Mashour GA, Roelfsema P, Changeux J-P, Dehaene S. 2020. Conscious processing and the global neuronal workspace hypothesis. Neuron 105(5):776–798. doi:10.1016/j.neuron.2020.01.026
Neupane S, Fiete I, Jazayeri M. 2024. Mental navigation in the primate entorhinal cortex. Nature 630(8017):704–711. doi:10.1038/s41586-024-07557-z
[dataset] Neupane S, Fiete I, Jazayeri M. 2024. Mental navigation in the primate entorhinal cortex. DANDI Archive, dandiset 000897. dandiarchive.org/dandiset/000897
Ostrow M, Eisen A, Kozachkov L, Fiete I. 2023. Beyond geometry: comparing the temporal structure of computation in neural circuits with dynamical similarity analysis. NeurIPS. arXiv:2306.10168
Schiereck SS, Pérez-Rivera DT, Mah A, DeMaegd ML, Hocker D, Ward RM, Savin C, Constantinople CM. 2026. The orbitofrontal cortex updates beliefs for state inference. Neuron 114(3):507–520.e8. doi:10.1016/j.neuron.2025.11.014
[dataset] Schiereck SS et al. 2026. Data from: The orbitofrontal cortex updates beliefs for state inference. Zenodo. doi:10.5281/zenodo.16997337
Searle JR. 2017. Biological naturalism. In: Schneider S, Velmans M, editors. The Blackwell Companion to Consciousness, 2nd ed. Wiley-Blackwell. p. 327–336. doi:10.1002/9781119132363.ch23
Soldado-Magraner J, Mante V, Sahani M. 2024. Inferring context-dependent computations through linear approximations of prefrontal cortex dynamics. Science Advances 10(51):eadl4743. doi:10.1126/sciadv.adl4743