Search arXivSearch

arXiv · 1806.04704

Sparse distributed representation, hierarchy, critical periods, metaplasticity: the keys to lifelong fixed-time learning and best-match retrieval

Abstract

Among the more important hallmarks of human intelligence, which any artificial general intelligence (AGI) should have, are the following. 1. It must be capable of on-line learning, including with single/few trials. 2. Memories/knowledge must be permanent over lifelong durations, safe from catastrophic forgetting. Some confabulation, i.e., semantically plausible retrieval errors, may gradually accumulate over time. 3. The time to both: a) learn a new item, and b) retrieve the best-matching / most relevant item(s), i.e., do similarity-based retrieval, must remain constant throughout the lifetime. 4. The system should never become full: it must remain able to store new information, i.e., make new permanent memories, throughout very long lifetimes. No artificial computational system has been shown to have all these properties. Here, we describe a neuromorphic associative memory model, Sparsey, which does, in principle, possess them all. We cite prior results supporting possession of hallmarks 1 and 3 and sketch an argument, hinging on strongly recursive, hierarchical, part-whole compositional structure of natural data, that Sparsey also possesses hallmarks 2 and 4.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Gerard Rinkus. 2018-06-02. Sparse distributed representation, hierarchy, critical periods, metaplasticity: the keys to lifelong fixed-time learning and best-match retrieval. https://arxiv.org/abs/1806.04704

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Only what exists can cause: An intrinsic powers view of free will

This essay addresses the implications of integrated information theory (IIT) for free will. IIT is a theory of what consciousness is and of how its presence and quality can be accounted for in physical terms. According to IIT, the presence of consciousness is accounted for by a maximum of cause-effect power in the brain. Moreover, the way an experience feels is accounted for by how that cause-effect power is structured. If IIT is right, we do have free will in a genuine sense: we have alternatives, reasons, and values, we make decisions, and we-not our neurons or atoms-are the cause of our willed actions and bear responsibility for them. IIT's argument for genuine free will hinges on the proper understanding of consciousness as intrinsic existence, captured by its intrinsic powers ontology: what exists absolutely, in physical terms, are intrinsic entities, and only what exists can cause.

q-bio.NC

Seeing the imagined: latent functional alignment in visual imagery decoding from fMRI data

Recent progress in visual brain decoding from fMRI has been enabled by large-scale datasets such as the Natural Scenes Dataset (NSD) and powerful diffusion-based generative models. While current pipelines are primarily optimized for perception, their performance under mental-imagery remains less well understood. In this work, we study how a state-of-the-art (SOTA) perception decoder (DynaDiff) can be adapted to reconstruct imagined content from the NSD-Imagery benchmark. We propose a latent functional alignment (LFA) approach that maps imagery-evoked activity to the pretrained model's semantic content-enriched conditioning space, by adding a simple alignment module, while keeping the original remaining components frozen. To mitigate the limited amount of matched imagery-perception supervision, we further introduce a neural retrieval-based augmentation strategy that selects semantically related NSD perception trials from the same participants. Across four subjects, LFA consistently improves high-level semantic reconstruction metrics relative to the frozen pretrained baseline and a voxel-space ridge alignment baseline, and enables above-chance decoding from multiple cortical regions. These results suggest that semantic structure learned from perception can be leveraged to stabilize and improve visual imagery decoding under out-of-distribution conditions.

q-bio.NC

Deep Learning in Infant Functional Neuroimaging: Challenges, Advances, and Future Directions

Infancy is a critical developmental window characterized by rapid functional brain reorganization, during which large-scale networks emerge, individualized connectome signatures continue to form, and early deviations may shape long-term cognitive and clinical outcomes. Functional MRI (fMRI) offers an opportunity to study these processes in vivo, yet extracting developmentally meaningful information from it remains challenging due to comparatively short scan duration, structured motion artifacts, variable scan states, and rapid brain maturation. Amid these challenges, deep learning has expanded the capacity of computational neuroimaging by learning robust representations from noisy, high-dimensional data, integrating complex spatial and temporal information, and capturing the nonlinear and rapidly evolving organization of the developing brain. Here, we review recent advances in deep learning for infant functional neuroimaging, synthesizing progress across input representation formatting, population and individualized brain mapping, longitudinal trajectory forecasting, robust and explainable model evaluation, and biological translation. Collectively, these methodological advances mark a paradigm shift in infant functional neuroimaging from descriptive, group-level analyses toward reliable, individualized, and developmentally grounded models. Future progress will depend on larger and more diverse longitudinal datasets, developmentally appropriate model designs, rigorous and standardized evaluation, and integration of computational predictions with biological mechanisms towards clinically meaningful outcomes. Addressing these priorities will help establish deep learning as a robust framework for understanding early functional brain development, identifying developmental variation at the individual level, and ultimately supporting earlier and precise assessment of neurodevelopmental risk.

q-bio.NC