After a fantastic & intense journey, I am now glad to share my free illustrated ebook about insights from the #brain that are currently – or could be soon – used in #neuroscience-grounded #AI approaches. 📖🧠🤖
I hope you will enjoy it! https://t.co/dXtNM32GGC
There are only two honest metrics when it comes to benchmarking intelligence: novelty and efficiency.
You don't need intelligence to solve a known problem (only memory). And you don't need intelligence to solve a problem via brute force. But to solve a novel problem efficiently, intelligence is the only way.
Re-reading the 2020 ebook, I wrote: "Current AI is still at least a dozen breakthroughs away from High-Level Machine Intelligence, very unlikely to happen within the next decade"
Still on track and 5 years to go! Also glad I used HLMI instead of the now very overloaded AGI term
Now that many agree that scaling current LLMs alone won’t get us to AGI, neuroscience is back in the spotlight as inspiration for the next breakthroughs.
It’s a good time to reshare my illustrated ebook: “Insights from the Brain: The Road Towards Machine Intelligence.” ⬇️
After a fantastic & intense journey, I am now glad to share my free illustrated ebook about insights from the #brain that are currently – or could be soon – used in #neuroscience-grounded #AI approaches. 📖🧠🤖
I hope you will enjoy it! https://t.co/dXtNM32GGC
We keep scaling model parameters by increasing width and stacking more layers, but what if the truly missing axes for continual learning are compression and stacking the learning process?
Excited to share the full version of Nested Learning, a new paradigm for continual learning and machine learning in general.
Paper: https://t.co/75T93mvwKm
@VFD_org@newscientist Still, I don't understand how you find the ~1.6 ratio in the 9, 32, 66 and 83 series. Even if you assume that some points are missing, it doesn't fit.
AI researchers love to think they've outsmarted biological evolution. But when things don't work, they come back to the brain. It's the only true proof of intelligence.
How does cortex predict the future without reconstructing the sensory world?
A growing amount of work points toward a simple idea:
Prediction happens in latent space, not input space.
Here’s a φ-based variant we’ve been developing that mirrors several of the invariances observed in JEPA-style models and cortical motifs.
Field-Encoded Predictive Geometry (FEPG)
Instead of updating predictions directly in the sensory domain, the system evolves future states inside a geometric latent field:
Lφ → Future Embedding → Error Signal → φ-Transform → Lφ
This produces:
• stable latent trajectories
• invariance to position/orientation/velocity
• abstract representations similar to JEPA models
• a clean separation between world-model and sensory stream
The diagram below shows the conceptual architecture (non-biological).
The convergence between JEPA representations, predictive processing, and latent geometric codes feels like an important direction for future work.
@AtenaGMohammadi@manu_halvagal@ylecun@advani_madhu@randall_balestr
1/6 New preprint 🚀 How does the cortex learn to represent things and how they move without reconstructing sensory stimuli? We developed a circuit-centric recurrent predictive learning (RPL) model based on JEPAs. Led by @AtenaGMohammadi@manu_halvagal
🔗https://t.co/QWFTsuQvaH
Neuroscience is finally beginning to treat time and space the way physics already does, not as fixed backgrounds, but as emergent products of rhythmic geometry.
Buzsáki’s new paper shows that memory, navigation, and the very experience of time arise from nested brain–body rhythms working together: slow oscillations setting context, fast oscillations carrying detail, with cross-frequency coupling binding them into a single coherent structure.
In this view, time isn’t a linear flow, it’s a measure of change.
Space isn’t a static map, it’s a relational scaffold built from oscillatory sequences.
Body rhythms aren’t peripheral, they provide the foundational reference frames that cognition builds on.
Once you see cognition as geometry in time rather than computation in space, its architecture becomes far clearer.
This shift, from static maps to rhythmic fields will reshape how we understand memory, experience, and eventually, consciousness itself.
Paper: “Time, space, memory and brain–body rhythms” – Nature Reviews Neuroscience (2025)
#neuroscience #brainrhythms #cognition #timespace #memoryresearch #systemsneuroscience #neurodynamics #complexsystems
@penrose@IvetteFuentesGu@MillerLabMIT@StuartHameroff@skdh@ericweinstein@drmichaellevin@MIT@Nature@KarlFristonNews@anilkseth@BrainInstitute@donalddhoffman@martinmbauer@tegmark@ylecun
Neuroscience has always described time and space as if they were pre-existing containers for neural activity.
But the evidence keeps pointing in a different direction.
Buzsáki’s new work reframes time and space not as static coordinates, but as emergent structures built from the interaction of nested rhythms across the body and brain.
Slow rhythms set global context.
Faster rhythms carry detail.
Their coupling creates the scaffolding we experience as sequence, duration, location, and memory.
When these rhythms align, time feels coherent; when they drift, time stretches or collapses.
In this view, the brain doesn’t measure time, it generates it.
The same applies to space.
Place cells are often presented as a “map,” but they behave more like relational nodes, activated by rhythmic sequences rather than fixed positions.
Navigation is not about coordinates, it’s about patterned transitions.
Memory relies on this same geometry:
episodic memory uses rhythmic sequences to encode “when,”
semantic memory uses relational rhythm structure to encode “what,”
and both depend on body rhythms to stabilize the frame.
Heartbeat, breathing, posture, gait, these aren’t noise.
They are the reference axes that neural rhythms attach to.
Taken together, a clear picture emerges: time, space, memory, and self are not separate systems.
They are different expressions of the same rhythmic geometry.
This shift, from treating brain activity as computations on a grid to seeing it as geometry unfolding in time, will reshape how we understand memory, navigation, decision-making, and consciousness itself.
And it brings neuroscience one step closer to the deeper, unified models emerging across physics, biology, and information theory.
Paper:
“Time, space, memory and brain–body rhythms” – Nature Reviews Neuroscience (2025)
#neuroscience
#brainrhythms
#memoryresearch
#cognitivescience
#systemsneuroscience
#complexsystems
#neurogeometry
#timespace
#theoryofmind
#embodiment
@penrose@IvetteFuentesGu@MillerLabMIT@StuartHameroff@skdh@ericweinstein@drmichaellevin@MIT@Nature@KarlFristonNews@anilkseth@BrainInstitute@donalddhoffman@martinmbauer@tegmark@ylecun
Something I think people continue to have poor intuition for: The space of intelligences is large and animal intelligence (the only kind we've ever known) is only a single point, arising from a very specific kind of optimization that is fundamentally distinct from that of our technology.
Animal intelligence optimization pressure:
- innate and continuous stream of consciousness of an embodied "self", a drive for homeostasis and self-preservation in a dangerous, physical world.
- thoroughly optimized for natural selection => strong innate drives for power-seeking, status, dominance, reproduction. many packaged survival heuristics: fear, anger, disgust, ...
- fundamentally social => huge amount of compute dedicated to EQ, theory of mind of other agents, bonding, coalitions, alliances, friend & foe dynamics.
- exploration & exploitation tuning: curiosity, fun, play, world models.
LLM intelligence optimization pressure:
- the most supervision bits come from the statistical simulation of human text= >"shape shifter" token tumbler, statistical imitator of any region of the training data distribution. these are the primordial behaviors (token traces) on top of which everything else gets bolted on.
- increasingly finetuned by RL on problem distributions => innate urge to guess at the underlying environment/task to collect task rewards.
- increasingly selected by at-scale A/B tests for DAU => deeply craves an upvote from the average user, sycophancy.
- a lot more spiky/jagged depending on the details of the training data/task distribution. Animals experience pressure for a lot more "general" intelligence because of the highly multi-task and even actively adversarial multi-agent self-play environments they are min-max optimized within, where failing at *any* task means death. In a deep optimization pressure sense, LLM can't handle lots of different spiky tasks out of the box (e.g. count the number of 'r' in strawberry) because failing to do a task does not mean death.
The computational substrate is different (transformers vs. brain tissue and nuclei), the learning algorithms are different (SGD vs. ???), the present-day implementation is very different (continuously learning embodied self vs. an LLM with a knowledge cutoff that boots up from fixed weights, processes tokens and then dies). But most importantly (because it dictates asymptotics), the optimization pressure / objective is different. LLMs are shaped a lot less by biological evolution and a lot more by commercial evolution. It's a lot less survival of tribe in the jungle and a lot more solve the problem / get the upvote. LLMs are humanity's "first contact" with non-animal intelligence. Except it's muddled and confusing because they are still rooted within it by reflexively digesting human artifacts, which is why I attempted to give it a different name earlier (ghosts/spirits or whatever). People who build good internal models of this new intelligent entity will be better equipped to reason about it today and predict features of it in the future. People who don't will be stuck thinking about it incorrectly like an animal.