Papers
Topics
Authors
Recent
Search
2000 character limit reached

On Conformal Isometry of Grid Cells: Learning Distance-Preserving Position Embedding

Published 27 May 2024 in q-bio.NC, cs.LG, and stat.ML | (2405.16865v4)

Abstract: This paper investigates the conformal isometry hypothesis as a potential explanation for the hexagonal periodic patterns in grid cell response maps. We posit that grid cell activities form a high-dimensional vector in neural space, encoding the agent's position in 2D physical space. As the agent moves, this vector rotates within a 2D manifold in the neural space, driven by a recurrent neural network. The conformal hypothesis proposes that this neural manifold is a conformal isometric embedding of 2D physical space, where local physical distance is preserved by the embedding up to a scaling factor (or unit of metric). Such distance-preserving position embedding is indispensable for path planning in navigation, especially planning local straight path segments. We conduct numerical experiments to show that this hypothesis leads to the hexagonal grid firing patterns by learning maximally distance-preserving position embedding, agnostic to the choice of the recurrent neural network. Furthermore, we present a theoretical explanation of why hexagon periodic patterns emerge by minimizing our loss function by showing that hexagon flat torus is maximally distance preserving.

Definition Search Book Streamline Icon: https://streamlinehq.com
References (60)
  1. A theory of joint attractor dynamics in the hippocampus and the entorhinal cortex accounts for artificial remapping and grid cell field-to-field variability. eLife, 9:e56894, 2020.
  2. Daniel J Amit. Modeling brain function: The world of attractor neural networks. Cambridge university press, 1992.
  3. Solid state physics, 1976.
  4. Vector-based navigation using grid-like representations in artificial agents. Nature, 557(7705):429, 2018.
  5. Experience-dependent rescaling of entorhinal grids. Nature neuroscience, 10(6):682–684, 2007.
  6. Navigating cognition: Spatial codes for human thinking. Science, 362(6415):eaat6766, 2018.
  7. Scale-invariant memory representations emerge from moire interference between grid fields that produce theta oscillations: a computational model. Journal of Neuroscience, 27(12):3211–3229, 2007.
  8. The entorhinal cognitive map is attracted to goals. Science, 363(6434):1443–1447, 2019.
  9. Accurate path integration in continuous attractor network models of grid cells. PLoS computational biology, 5(2):e1000291, 2009.
  10. Organizing conceptual knowledge in humans with a gridlike code. Science, 352(6292):1464–1468, 2016.
  11. Recurrent inhibitory circuitry as a mechanism for grid formation. Nature neuroscience, 16(3):318–324, 2013.
  12. Emergence of grid-like representations by training recurrent neural networks to perform spatial localization. arXiv preprint arXiv:1803.07770, 2018.
  13. Emergence of functional and structural properties of the head direction system by optimization of recurrent neural networks. International Conferences on Learning Representations (ICLR), 2020.
  14. The input–output transformation of the hippocampal granule cells: from grid cells to place fields. Journal of Neuroscience, 29(23):7504–7512, 2009.
  15. Evidence for grid cells in a human memory network. Nature, 463(7281):657, 2010.
  16. Extracting grid cell characteristics from place cell inputs using non-negative principal component analysis. Elife, 5:e10094, 2016.
  17. Actionable neural representations: Grid cells from minimal constraints. arXiv preprint arXiv:2209.15563, 2022.
  18. William Gerard Dwyer and CW Wilkerson. The elementary geometric structure of compact lie groups. Bulletin of the London Mathematical Society, 30(4):337–364, 1998.
  19. What grid cells convey about rat location. Journal of Neuroscience, 28(27):6858–6871, 2008.
  20. A spin glass model of path integration in rat medial entorhinal cortex. Journal of Neuroscience, 26(16):4266–4276, 2006.
  21. Spatial representation in the entorhinal cortex. Science, 305(5688):1258–1264, 2004.
  22. Grid cells in mice. Hippocampus, 18(12):1230–1238, 2008.
  23. Learning grid cells as vector representation of self-position coupled with matrix representation of self-motion. In International Conference on Learning Representations, 2019.
  24. On path integration of grid cells: group representation and isotropic scaling. In Neural Information Processing Systems, 2021.
  25. Toroidal topology of population activity in grid cells. bioRxiv, 2021.
  26. Impaired path integration in mice with disrupted grid cell firing. Nature neuroscience, 21(1):81–91, 2018.
  27. Are grid cells used for navigation? on local metrics, subjective spaces, and black holes. Neuron, 111(12):1858–1875, 2023.
  28. Microstructure of a spatial map in the entorhinal cortex. Nature, 436(7052):801, 2005.
  29. Grid-like processing of imagined navigation. Current Biology, 26(6):842–847, 2016.
  30. Direct recordings of grid-like neuronal activity in human spatial navigation. Nature neuroscience, 16(9):1188, 2013.
  31. A map of visual space in the primate entorhinal cortex. Nature, 491(7426):761, 2012.
  32. Adam: A method for stochastic optimization. arXiv preprint arXiv:1412.6980, 2014.
  33. Development of the spatial representation system in the rat. Science, 328(5985):1576–1580, 2010.
  34. Path integration and the neural basis of the’cognitive map’. Nature Reviews Neuroscience, 7(8):663, 2006.
  35. Where am i? where am i going? Scientific American, 314(1):26–33, 2016.
  36. Explaining heterogeneity in medial entorhinal cortex with task-driven neural networks. Advances in Neural Information Processing Systems, 34:12167–12179, 2021.
  37. The hippocampus as a spatial map: preliminary evidence from unit activity in the freely-moving rat. Brain research, 1971.
  38. Précis of o’keefe & nadel’s the hippocampus as a cognitive map. Behavioral and Brain Sciences, 2(4):487–494, 1979.
  39. Feedback inhibition enables theta-nested gamma oscillations and grid firing fields. Neuron, 77(1):141–154, 2013.
  40. Impaired speed encoding is associated with reduced grid cell periodicity in a mouse model of tauopathy. bioRxiv, page 595652, 2019.
  41. Functional properties of stellate cells in medial entorhinal cortex layer ii. Elife, 7:e36664, 2018.
  42. Conjunctive representation of position, direction, and velocity in entorhinal cortex. Science, 312(5774):758–762, 2006.
  43. Spectral methods for dimensionality reduction. Semi-supervised learning, 3, 2006.
  44. No free lunch from deep learning in neuroscience: A case study through models of the entorhinal-hippocampal circuit. Advances in Neural Information Processing Systems, 35:16052–16067, 2022.
  45. Self-supervised learning of representations for space generates multi-modular grid cells. arXiv preprint arXiv:2311.02316, 2023.
  46. Coherently remapping toroidal cells but not grid cells are responsible for path integration in virtual agents. bioRxiv, pages 2022–08, 2022.
  47. Hexagons all the way down: Grid cells as a conformal isometric map of space. bioRxiv, pages 2024–02, 2024.
  48. A unified theory for the origin of grid cells through the lens of pattern formation. Advances in neural information processing systems, 32, 2019.
  49. A unified theory for the computational and mechanistic origins of grid cells. Neuron, 111(1):121–137, 2023.
  50. Grid cells generate an analog error-correcting code for singularly precise neural computation. Nature neuroscience, 14(10):1330, 2011.
  51. The hippocampus as a predictive map. Nature neuroscience, 20(11):1643, 2017.
  52. Connecting multiple spatial scales to decode the population activity of grid cells. Science Advances, 1(11):e1500816, 2015.
  53. The entorhinal grid map is discretized. Nature, 492(7427):72, 2012.
  54. Edward C Tolman. Cognitive maps in rats and men. Psychological review, 55(4):189, 1948.
  55. Attention is all you need. Advances in neural information processing systems, 30, 2017.
  56. A principle of economy predicts the functional architecture of grid cells. Elife, 4:e08362, 2015.
  57. Relating transformers to models and neural representations of the hippocampal formation. arXiv preprint arXiv:2112.04035, 2021.
  58. Conformal isometry of lie group representation in recurrent network of grid cells. arXiv preprint arXiv:2210.02684, 2022.
  59. Grid cells without theta oscillations in the entorhinal cortex of bats. Nature, 479(7371):103, 2011.
  60. Optogenetic dissection of entorhinal-hippocampal functional connectivity. Science, 340(6128), 2013.
Citations (1)

Summary

  • The paper introduces a novel framework leveraging conformal isometry to explain hexagonal grid cell patterns.
  • It validates the theory through both linear and nonlinear models, demonstrating consistent pattern emergence with varying scale factors.
  • The findings have implications for neuroscience and AI, enhancing spatial navigation models through conformal modulation techniques.

Learning Distance-Preserving Position Embedding: An Analysis of "On Conformal Isometry of Grid Cells"

This essay explores the "On Conformal Isometry of Grid Cells: Learning Distance-Preserving Position Embedding" paper, which explores the usage of the conformal isometry hypothesis to explain grid cells' hexagonal firing patterns. By evaluating grid cells, which are integral to the mammalian brain's spatial navigation processes, the authors postulate a mathematical framework that provides both numerical and theoretical validation for the hypothesis.

Introduction to Grid Cell Conformal Isometry

The conformal isometry hypothesis is pivotal in understanding how grid cells' firing patterns form an internal map analogous to a GPS within the brain. As an animal navigates through a 2D physical space, grid cells preserve spatial distances through high-dimensional vector arrangements. The hypothesis suggests that these vectors rotate on a 2D manifold that maintains proportionality to physical space movements via conformal isometry, effectively mapping a 2D surface as a neural representation.

Numerical Experiments and Models

The paper employs a minimalistic model of grid cells, focusing on exploring grid patterns using conformal isometry. By analyzing both linear and nonlinear transformation models, the study reveals that hexagon patterns emerge robustly across different setups. For instance, experiments display how varying the scale factor ss in linear models changes grid scale, highlighting the hexagon formation. This supports the notion of conformal embeddings that map physical movements into neural actuations naturally. Figure 1

Figure 1

Figure 1: Hexagonal patterns learned in linear models. (a) Learned patterns of linear model with different scales. (b) Toroidal structure spectral analysis of the activities of grid cells.

Torus Topology and Frequency Analysis

Theoretically, the learned patterns map onto a toroidal manifold in neural space, as identified via spectral analysis, which evaluates periodicity and reveals hexagonal distribution of Fourier components. The paper makes these connections explicit through Fourier analysis, demonstrating that 2D periodic publishing in frequency space manifests in grid-like regularities, integral for stable spatial representation. This aligns grid cell modelling with physical principles seen in crystallographic lattice structures. Figure 2

Figure 2: 2D periodic lattice is defined by two primitive vectors.

Conformal Modulation Techniques

One key aspect of the paper is the introduction of conformal modulation to neural networks. This technique evaluates and adjusts the input velocity of grid cells to preserve isometry across transformations, enhancing the adherence to the conformal isometry hypothesis. Experiments with and without this modulation show significant improvements in maintaining accurate path integration, supporting compliant mapping between neural and spatial geometries.

Implications for Neuroscience and AI

The exploration of hexagonal grid cell patterns under conformal conditions not only strengthens our understanding of biological navigation systems but also introduces fundamental principles in neural network design for AI applications. By leveraging such geometric insights, one might enhance the capacity of computational models performing spatial reasoning tasks, including robotic navigation and autonomous systems.

Conclusion

This paper provides both experimental and theoretical backing of the conformal isometry hypothesis as a fitting explanation for the consistent emergence of hexagonal patterns in grid cells. By introducing novel modulation techniques and thorough numerical validation, the authors cement a pathway through which mathematical models can explain, predict, and potentially manipulate navigational processes within both biological and artificial systems. Figure 3

Figure 3

Figure 3: Results of the non-linear models. We randomly chose 8 modules and showed the firing patterns with different rectification functions.

Ultimately, it propels the advancement of neural architecture understanding and its seamless applications in modeling spatial and cognitive representations in AI systems.

Paper to Video (Beta)

Whiteboard

No one has generated a whiteboard explanation for this paper yet.

Open Problems

We haven't generated a list of open problems mentioned in this paper yet.

Collections

Sign up for free to add this paper to one or more collections.

Tweets

Sign up for free to view the 2 tweets with 1 like about this paper.