Get AI summaries of any video or article — Sign up free
What’s Your Brain’s Role in Creating Space & Time? thumbnail

What’s Your Brain’s Role in Creating Space & Time?

PBS Space Time·
6 min read

Based on PBS Space Time's video on YouTube. If you like this content, support the original creators by watching, liking and subscribing to their content.

TL;DR

Place cells (hippocampus) fire for specific locations and remap when the environment changes, providing a location-linked code.

Briefing

The brain’s internal machinery for “space and time” looks less like a passive mirror of the universe and more like a flexible system for organizing relationships—between locations, motions, and even sequences of events. That matters because many physicists now suspect spacetime may not be a fundamental entity, and neuroscience is offering a way to test whether brains can generate “spacetime-like” structure from underlying regularities rather than from spacetime itself.

Work on navigation in mammals points to a coordinated set of neural maps. In 1971, John O’Keefe and Jonothon Dostrovsky identified hippocampal “place cells” in rats: specific neurons fire when the animal enters particular regions of an environment, then “remap” when the rat moves to a new space. Later, in 2005, Edvard and May-britt Moser discovered grid cells in the entorhinal cortex. These neurons fire not only at one location, but across multiple locations that form a repeating hexagonal grid spanning the current environment. Different grid cells correspond to different spatial scales, acting like a set of rulers that provide metric information. The firing of grid cells is thought to combine—possibly through an inverse Fourier-transform-like computation—to activate localized place cells, yielding a unique neural signature for each location.

At first glance, this resembles an “absolute” Newtonian picture: a coordinate-like grid fixed to the environment, independent of the animal’s position within it and independent of the objects inside it. But the system also depends on relational inputs. Brains update the allocentric map using egocentric information—depth perception to help construct the grid and internal signals about velocity and direction to keep the map aligned as the animal moves. The result is a space representation that feels absolute in structure while being continuously rebuilt from relationships among self-motion, sensory cues, and external layout.

Time is treated similarly. Newton’s view of time as an independent cosmic clock is contrasted with Einstein’s line that “Time is what clocks measure,” implying time emerges from matter’s behavior. Neuroscience supports the idea that humans track time without a single universal internal clock. Instead, different brain regions likely model timing across scales using rhythmic neural activity (with brain waves ranging roughly from 0.02 to 600 Hz), circadian cycles, memory dynamics, and other mechanisms. Short-interval timing is relatively consistent, while longer estimates degrade and become strongly influenced by context.

The most consequential twist comes when space and time blur inside the hippocampus. Under some conditions, hippocampal cells appear to track progression of time even when a rat runs in place, and place cells can fire for new locations or for the passage of time. During theta cycles (4–10 Hz) in the hippocampus, sequences of place-cell activity can represent the recent past and upcoming trajectory, suggesting the hippocampal code may track executed and planned paths—potentially in abstract “thought space” as well as physical space. Because the hippocampus is central to memory sequencing, the same navigation machinery may have been co-opted to organize events and relationships more generally.

The upshot: neuroscience can’t settle whether spacetime is physically real, but it shows brains are capable of generating spacetime-like structure from general-purpose algorithms that map relationships among continuous variables and sequences of events. If that’s true, then spacetime’s perceived primacy may reflect how brains partition experience—efficiently and inevitably—rather than guaranteeing that spacetime is a fundamental ingredient of reality.

Cornell Notes

Neuroscience suggests the brain builds “space and time” using neural maps and timing mechanisms that organize relationships, not necessarily by reading out a fundamental spacetime structure. Place cells (hippocampus) fire for specific locations and remap when environments change. Grid cells (entorhinal cortex) tile environments with hexagonal patterns across multiple spatial scales, providing metric-like information that helps drive place-cell activity. Timekeeping appears distributed across brain rhythms, circadian cycles, memory dynamics, and other internal processes rather than a single cosmic clock. Crucially, hippocampal activity can reflect sequences and trajectories—sometimes time progression rather than location—hinting that the same machinery may support navigation in both physical and abstract spaces.

How do place cells and grid cells work together to represent where an animal is?

Place cells in the hippocampus fire when a rat enters a particular region of an environment and remain tied to that location until the rat moves to a new environment, at which point the pattern remaps. Grid cells in the entorhinal cortex fire when the rat passes through locations that collectively form a hexagonal grid spanning the current space. Individual grid cells correspond to fixed spatial scales (e.g., firing every ~3 meters for one cell, ~1 meter for another, ~10 meters for another), and the combination of multiple grid-cell signals is thought to activate localized place cells—potentially via an inverse Fourier-transform-like computation. The result is a unique firing pattern for each location.

Why does grid-cell activity feel “absolute,” even though it depends on relational information?

Grid cells appear to provide a coordinate-like tiling of the environment: the grid is fixed to the current space and does not directly depend on where the animal is within it. That makes the representation resemble an absolute, Newtonian-style spatial framework. But the brain must update that framework using relational cues—egocentric processing such as depth perception helps construct the grid, while internal estimates of velocity and direction update the animal’s position on the grid as it moves. So the map’s structure can be environment-centered while the updating process is relationship-based.

What evidence supports the idea that the brain’s sense of time is not a single “master clock”?

Humans can track time, but neuroscience generally does not support one universal internal clock. Different brain regions likely model timing on different scales. Rhythmic neural activity is a leading candidate: brain waves repeat across a wide frequency range (about 0.02 to 600 Hz), and some rhythms may coordinate other neurons like a timing scaffold. Timing also involves circadian rhythms, memory accumulation and ordering, and other neural methods. Short intervals are estimated more accurately and consistently than longer ones, which tend to degrade and become context-dependent.

How can hippocampal cells represent time as well as (or instead of) space?

Under certain conditions, hippocampal cells can track progression of time rather than location. For example, cells may fire sequentially as time passes when a rat runs in a wheel (so the animal’s physical position doesn’t change in the usual way). More broadly, place cells can fire for new locations or for the passage of time, suggesting a more general role in tracking sequences. This aligns with the idea that hippocampal coding may reflect trajectories—what the animal has done and what it is about to do—rather than strictly mapping physical coordinates.

What does theta activity imply about how the hippocampus encodes past and future?

Theta cycles in the hippocampus—periodic neuronal pulsing at roughly 4–10 Hz—organize rapid sequences of place-cell firing. During each theta pulse, a chain of place cells fires in succession: neurons representing the recent past activate first, then a neuron representing the current location or time, followed by neurons representing upcoming places in the trajectory. The brain therefore “lives” across immediate past and future within each theta cycle, supporting a trajectory-based interpretation of hippocampal function.

How does this neuroscience connect to the philosophical debate about space and time?

Philosophical positions range from Newton’s absolute view (space and time exist independently) to relational views (space as distances between objects, time as succession of events) and Kant’s idea that space and time are mind constructs. Einstein’s framing—“Time is what clocks measure”—pushes toward time emerging from matter. Neuroscience doesn’t directly prove which metaphysics is correct, but it shows brains can generate structured representations of space and time using general-purpose algorithms for mapping relationships and sequences. That supports the plausibility that spacetime-like regularities could be brain-partitioned features of deeper external structure.

Review Questions

  1. What specific firing properties distinguish place cells from grid cells, and how do those properties change when an animal enters a new environment?
  2. Why might hippocampal place-cell sequences be better interpreted as tracking trajectories or sequences rather than strictly encoding physical location?
  3. What kinds of neural mechanisms are proposed for time perception, and how do their behaviors differ across short versus long timescales?

Key Points

  1. 1

    Place cells (hippocampus) fire for specific locations and remap when the environment changes, providing a location-linked code.

  2. 2

    Grid cells (entorhinal cortex) fire across multiple locations arranged in hexagonal patterns, tiling the environment at multiple fixed spatial scales.

  3. 3

    The brain likely combines signals from multiple grid cells to drive localized place-cell activation, potentially using computations akin to an inverse Fourier transform.

  4. 4

    Spatial representation can look environment-centered and coordinate-like, but it is continually updated using relational egocentric inputs such as velocity, direction, and depth cues.

  5. 5

    Time perception appears distributed across multiple internal mechanisms (neural rhythms, circadian cycles, memory dynamics) rather than relying on a single master clock.

  6. 6

    Hippocampal activity can reflect time progression and planned/executed trajectories, blurring the boundary between “space” and “time” codes.

  7. 7

    Neuroscience supports the idea that brains can construct spacetime-like structure from general algorithms that map relationships and sequences, even if spacetime itself is not fundamental.

Highlights

Grid cells tile environments with hexagonal firing fields across multiple scales, acting like a metric ruler system that helps define where an animal is.
Place cells can remap to new environments, but hippocampal sequences can also track time progression—suggesting a broader “sequence/trajectory” function.
Theta cycles (4–10 Hz) organize hippocampal firing so that each cycle spans recent past, current state, and upcoming trajectory.
Timekeeping in the brain is likely distributed across rhythms and memory processes, making experienced time malleable rather than absolute.

Topics

Mentioned