Recent proposals suggest that large, generic neuronal networks could store memory traces of past input sequences in their instantaneous state. Such a proposal raises important theoretical questions about the duration of these memory traces and their dependence on network size, connectivity and signal statistics. Prior work, in the case of gaussian input sequences and linear neuronal networks, shows that the duration of memory traces in a network cannot exceed the number of neurons (in units of the neuronal time constant), and that no network can out-perform an equivalent feedforward network. However a more ethologically relevant scenario is that of sparse input sequences. In this scenario, we show how linear neural networks can essentially perform compressed sensing (CS) of past inputs, thereby attaining a memory capacity that exceeds the number of neurons. This enhanced capacity is achieved by a class of "orthogonal" recurrent networks and not by feedforward networks or generic recurrent networks. We exploit techniques from the statistical physics of disordered systems to analytically compute the decay of memory traces in such networks as a function of network size, signal sparsity and integration time. Alternately, viewed purely from the perspective of CS, this work introduces a new ensemble of measurement matrices derived from dynamical systems, and provides a theoretical analysis of their asymptotic performance.

An incredible gulf separates theoretical models of synapses, often described solely by a single scalar value denoting the size of a postsynaptic potential, from the immense complexity of molecular signaling pathways underlying real synapses. To understand the functional contribution of such molecular complexity to learning and memory, it is essential to expand our theoretical conception of a synapse from a single scalar to an entire dynamical system with many internal molecular functional states. Moreover, theoretical considerations alone demand such an expansion; network models with scalar synapses assuming finite numbers of distinguishable synaptic strengths have strikingly limited memory capacity. This raises the fundamental question, how does synaptic complexity give rise to memory? To address this, we develop new mathematical theorems elucidating the relationship between the structural organization and memory properties of complex synapses that are themselves molecular networks. Moreover, in proving such theorems, we uncover a framework, based on first passage time theory, to impose an order on the internal states of complex synaptic models, thereby simplifying the relationship between synaptic structure and function.

Recurrent Neural Networks (RNNs) are among the most widely used machine learning tools for sequential data processing [Suts 14]. Despite the rising popularity of transformer deep neural architectures [Vasw 17, Gali 22, Acci 23], in particular, in natural language processing, RNNs remain more suitable in a significant range of real-time and online learning tasks that require handling one element of the sequence at a time. The key difference is that transformers are designed to process entire time sequences at once, using self-attention mechanisms to focus on particular entries of the input, while RNNs use hidden state spaces to retain a memory of previous elements in the input sequence, which makes memory one of the most important features of RNNs. Multiple attempts have been made in recent years to design quantitative measures and characterize memory in neural networks in general [Vers 20, Koyu 23] and their recurrent versions, in particular, [Havi 19, Li 21]. The notion of memory capacity (MC) in recurrent neural networks was first introduced in [Jaeg 02], with a particular focus on the so-called echo state networks (ESNs) [Matt 92, Matt 94, Jaeg 04], which are a popular family of RNNs within the reservoir computing (RC) strand of the literature that have shown to be universal approximants in various contexts [Grig 18, Gono 20b, Gono 21]. RC models are state-space systems whose state map parameters are randomly generated and which can be seen as RNNs with random inner neuron connection weights and a readout layer that is trained depending on the learning task of interest.

An incredible gulf separates theoretical models of synapses, often described solely by a single scalar value denoting the size of a postsynaptic potential, from the immense complexity of molecular signaling pathways underlying real synapses. To understand the functional contribution of such molecular complexity to learning and memory, it is essential to expand our theoretical conception of a synapse from a single scalar to an entire dynamical system with many internal molecular functional states. Moreover, theoretical considerations alone demand such an expansion; network models with scalar synapses assuming finite numbers of distinguishable synaptic strengths have strikingly limited memory capacity. This raises the fundamental question, how does synaptic complexity give rise to memory? To address this, we develop new mathematical theorems elucidating the relationship between the structural organization and memory properties of complex synapses that are themselves molecular networks. Moreover, in proving such theorems, we uncover a framework, based on first passage time theory, to impose an order on the internal states of complex synaptic models, thereby simplifying the relationship between synaptic structure and function.

Recent proposals suggest that large, generic neuronal networks could store memory traces of past input sequences in their instantaneous state. Such a proposal raises important theoretical questions about the duration of these memory traces and their dependence on network size, connectivity and signal statistics. Prior work, in the case of gaussian input sequences and linear neuronal networks, shows that the duration of memory traces in a network cannot exceed the number of neurons (in units of the neuronal time constant), and that no network can out-perform an equivalent feedforward network. However a more ethologically relevant scenario is that of sparse input sequences. In this scenario, we show how linear neural networks can essentially perform compressed sensing (CS) of past inputs, thereby attaining a memory capacity that {\it exceeds} the number of neurons. This enhanced capacity is achieved by a class of ``orthogonal recurrent networks and not by feedforward networks or generic recurrent networks. We exploit techniques from the statistical physics of disordered systems to analytically compute the decay of memory traces in such networks as a function of network size, signal sparsity and integration time. Alternately, viewed purely from the perspective of CS, this work introduces a new ensemble of measurement matrices derived from dynamical systems, and provides a theoretical analysis of their asymptotic performance."