The hippocampal formation is home to some of the most intriguing neural codes in systems neuroscience. Low-dimensional spatial representation in the form of place cells, grid cells, head direction cells, and vectorial codes [1,2] are thought to underpin a neural basis for spatial navigation and memory [3,4]. Yet despite decades of intensive research, fundamental questions about the nature of these representations remain unresolved, and in some cases, actively contested. This workshop brings together leading and emerging scientists to interrogate, debate, and stress-test prevailing frameworks in the field. Rather than presenting a consensus view, we embrace productive disagreement as a scientific tool. Our format is deliberately confrontational in the best sense: pairs of researchers will stake out and defend positions (ideally opposing ones) in brief position statements. This will be followed by open, discussion-led sessions in which the audience is an active participant. Brevity in presentation is the goal, in order to maximize time for genuine scientific discussion. A central tension animating the workshop is the apparent divergence in spatial coding across species [5]. Rodent hippocampal place cells have long served as the canonical model of allocentric spatial representation, yet findings in non-human primates reveal a rather different picture [6], with neurons encoding spatial views rather than locations per se. Human place cells [7] seem much rarer than in the rodent. However, the workshop will not accept this as a clean separation. Instead the participants will ask if this apparent dichotomy reflects fundamental differences in the computational principles between the brains of different species, behavioral differences, or potentially experimental idiosyncrasies. Similarly, the discovery of grid cells transformed our understanding of spatial computation, offering what seems like an elegant solution to path integration through a metric, Euclidean representation of space [8]. Yet this canonical view is now under pressure from multiple directions [9]. Newer findings show that subsets of grid cells can encode future rather than current positions [10], grids deform in some environments [11], and appear to re-anchor mid-task [12] in certain experiments (i.e., they appear to operate in multiple reference frames). Theoretical accounts offer multiple responses, from attractor network models to eigenvector decompositions of environmental occupancy, each capturing some features of the data while struggling with others. These are two examples where productive debate and fresh ideas are needed. Overall the workshop will cover the following topics: Place cells in humans versus rodents: are we studying the same phenomenon? Grid cells and path integration: how tight is the link, and what breaks it? Can classical theories of grid cells as metric representations survive new challenges — including future-position coding, multiple reference frames, distortions of grid geometry, and eigenvector accounts of grid cell activity? Spatial view cells in monkeys: a fundamentally different solution, or a variation on a theme? The nature of representational drift in the hippocampal system: noise, reorganisation, or something more principled? Is the hippocampal system fundamentally spatial (and innate) or are place cells and related representations learned? Is human navigation in complex environments supported by the same hippocampal place cell map seen in rodents, or are there new computational principles in the human brain?
References:
[1] Moser, E. I., Kropff, E., & Moser, M. B. (2008). Place cells, grid cells, and the brain’s spatial representation system. Annu. Rev. Neurosci., 31(1), 69-89.
[2] Bicanski, A., & Burgess, N. (2020). Neuronal vector coding in spatial cognition. Nature Reviews Neuroscience, 21(9), 453-470.
[3] McNaughton, B. L., Battaglia, F. P., Jensen, O., Moser, E. I., & Moser, M. B. (2006). Path integration and the neural basis of the’cognitive map’. Nature Reviews Neuroscience, 7(8), 663-678. [4] Eichenbaum, H., & Cohen, N. J. (2014). Can we reconcile the declarative memory and spatial navigation views on hippocampal function?. Neuron, 83(4), 764-770.
[5] Olafsdottir, F., Epstein, R., Bicanski, A., Jacobs, J., Kunz, L., Donato, F., … & Newcombe, N. S. (2026, January). Integrating across levels-from cells and circuits to brains and behavior. In Ernst Strüngmann Forum 2024 on Navigation. [6] Rolls, E. T. (1999). Spatial view cells and the representation of place in the primate hippocampus. Hippocampus, 9(4), 467-480.
[7] Mao, D. (2023). Neural correlates of spatial navigation in primate hippocampus. Neuroscience Bulletin, 39(2), 315-327.
[8] Bush, D., Barry, C., Manson, D., & Burgess, N. (2015). Using grid cells for navigation. Neuron, 87(3), 507-520.
[9] Ginosar, G., Aljadeff, J., Las, L., Derdikman, D., & Ulanovsky, N. (2023). Are grid cells used for navigation? On local metrics, subjective spaces, and black holes. Neuron, 111(12), 1858-1875.
[10] Ouchi, A. (2026). Predictive grid cells: Future spatial representations in the hippocampal-entorhinal circuit. Neuroscience Research, 105053.
[11] Krupic, J., Bauza, M., Burton, S., Barry, C., & O’Keefe, J. (2015). Grid cell symmetry is shaped by environmental geometry. Nature, 518(7538), 232-235.
[12] Peng, J.-J., Throm, B., Najafian Jazi, M., Yen, T.-Y., Pizzarelli, R., Monyer, H., & Allen, K. (2025). Grid cells accurately track movement during path integration-based navigation despite switching reference frames. Nature Neuroscience.