Artificial ontogenesis: a connectionist model of development

This thesis suggests that ontogenetic adaptive processes are important for generating intelligent beha- viour. It is thus proposed that such processes, as they occur in nature, need to be modelled and that such a model could be used for generating artificial intelligence, and specifically robotic intelligence. Hence, this thesis focuses on how mechanisms of intelligence are specified.A major problem in robotics is the need to predefine the behaviour to be followed by the robot. This makes design intractable for all but the simplest tasks and results in controllers that are specific to that particular task and are brittle when faced with unforeseen circumstances. These problems can be resolved by providing the robot with the ability to adapt the rules it follows and to autonomously create new rules for controlling behaviour. This solution thus depends on the predefinition of how rules to control behaviour are to be learnt rather than the predefinition of rules for behaviour themselves.Learning new rules for behaviour occurs during the developmental process in biology. Changes in the structure of the cerebral 'cortex underly behavioural and cognitive development throughout infancy and beyond. The uniformity of the neocortex suggests that there is significant computational uniformity across the cortex resulting from uniform mechanisms of development, and holds out the possibility of a general model of development. Development is an interactive process between genetic predefinition and environmental influences. This interactive process is constructive: qualitatively new behaviours are learnt by using simple abilities as a basis for learning more complex ones. The progressive increase in competence, provided by development, may be essential to make tractable the process of acquiring higher -level abilities.While simple behaviours can be triggered by direct sensory cues, more complex behaviours require the use of more abstract representations. There is thus a need to find representations at the correct level of abstraction appropriate to controlling each ability. In addition, finding the correct level of abstrac- tion makes tractable the task of associating sensory representations with motor actions. Hence, finding appropriate representations is important both for learning behaviours and for controlling behaviours. Representations can be found by recording regularities in the world or by discovering re- occurring pat- terns through repeated sensory -motor interactions. By recording regularities within the representations thus formed, more abstract representations can be found. Simple, non -abstract, representations thus provide the basis for learning more complex, abstract, representations.A modular neural network architecture is presented as a basis for a model of development. The pat- tern of activity of the neurons in an individual network constitutes a representation of the input to that network. This representation is formed through a novel, unsupervised, learning algorithm which adjusts the synaptic weights to improve the representation of the input data. Representations are formed by neurons learning to respond to correlated sets of inputs. Neurons thus became feature detectors or pat- tern recognisers. Because the nodes respond to patterns of inputs they encode more abstract features of the input than are explicitly encoded in the input data itself. In this way simple representations provide the basis for learning more complex representations. The algorithm allows both more abstract represent- ations to be formed by associating correlated, coincident, features together, and invariant representations to be formed by associating correlated, sequential, features together.The algorithm robustly learns accurate and stable representations, in a format most appropriate to the structure of the input data received: it can represent both single and multiple input features in both the discrete and continuous domains, using either topologically or non -topologically organised nodes. The output of one neural network is used to provide inputs for other networks. The robustness of the algorithm enables each neural network to be implemented using an identical algorithm. This allows a modular `assembly' of neural networks to be used for learning more complex abilities: the output activations of a network can be used as the input to other networks which can then find representations of more abstract information within the same input data; and, by defining the output activations of neurons in certain networks to have behavioural consequences it is possible to learn sensory -motor associations, to enable sensory representations to be used to control behaviour

Lifelong Learning of Spatiotemporal Representations with Dual-Memory Recurrent Self-Organization

Artificial autonomous agents and robots interacting in complex environments are required to continually acquire and fine-tune knowledge over sustained periods of time. The ability to learn from continuous streams of information is referred to as lifelong learning and represents a long-standing challenge for neural network models due to catastrophic forgetting. Computational models of lifelong learning typically alleviate catastrophic forgetting in experimental scenarios with given datasets of static images and limited complexity, thereby differing significantly from the conditions artificial agents are exposed to. In more natural settings, sequential information may become progressively available over time and access to previous experience may be restricted. In this paper, we propose a dual-memory self-organizing architecture for lifelong learning scenarios. The architecture comprises two growing recurrent networks with the complementary tasks of learning object instances (episodic memory) and categories (semantic memory). Both growing networks can expand in response to novel sensory experience: the episodic memory learns fine-grained spatiotemporal representations of object instances in an unsupervised fashion while the semantic memory uses task-relevant signals to regulate structural plasticity levels and develop more compact representations from episodic experience. For the consolidation of knowledge in the absence of external sensory input, the episodic memory periodically replays trajectories of neural reactivations. We evaluate the proposed model on the CORe50 benchmark dataset for continuous object recognition, showing that we significantly outperform current methods of lifelong learning in three different incremental learning scenario

Somatodendritic consistency check for temporal feature segmentation

The brain identifies potentially salient features within continuous information streams to process hierarchical temporal events. This requires the compression of information streams, for which effective computational principles are yet to be explored. Backpropagating action potentials can induce synaptic plasticity in the dendrites of cortical pyramidal neurons. By analogy with this effect, we model a self-supervising process that increases the similarity between dendritic and somatic activities where the somatic activity is normalized by a running average. We further show that a family of networks composed of the two-compartment neurons performs a surprisingly wide variety of complex unsupervised learning tasks, including chunking of temporal sequences and the source separation of mixed correlated signals. Common methods applicable to these temporal feature analyses were previously unknown. Our results suggest the powerful ability of neural networks with dendrites to analyze temporal features. This simple neuron model may also be potentially useful in neural engineering applications

Selection of cortical dynamics for motor behaviour by the basal ganglia

The basal ganglia and cortex are strongly implicated in the control of motor preparation and execution. Re-entrant loops between these two brain areas are thought to determine the selection of motor repertoires for instrumental action. The nature of neural encoding and processing in the motor cortex as well as the way in which selection by the basal ganglia acts on them is currently debated. The classic view of the motor cortex implementing a direct mapping of information from perception to muscular responses is challenged by proposals viewing it as a set of dynamical systems controlling muscles. Consequently, the common idea that a competition between relatively segregated cortico-striato-nigro-thalamo-cortical channels selects patterns of activity in the motor cortex is no more suf?cient to explain how action selection works. Here, we contribute to develop the dynamical view of the basal ganglia-cortical system by proposing a computational model in which a thalamo-cortical dynamical neural reservoir is modulated by disinhibitory selection of the basal ganglia guided by top-down information, so that it responds with different dynamics to the same bottom-up input. The model shows how different motor trajectories can so be produced by controlling the same set of joint actuators. Furthermore, the model shows how the basal ganglia might modulate cortical dynamics by preserving coarse-grained spatiotemporal information throughout cortico-cortical pathways

Neuronal oscillations, information dynamics, and behaviour: an evolutionary robotics study

Oscillatory neural activity is closely related to cognition and behaviour, with synchronisation mechanisms playing a key role in the integration and functional organization of different cortical areas. Nevertheless, its informational content and relationship with behaviour - and hence cognition - are still to be fully understood. This thesis is concerned with better understanding the role of neuronal oscillations and information dynamics towards the generation of embodied cognitive behaviours and with investigating the efficacy of such systems as practical robot controllers. To this end, we develop a novel model based on the Kuramoto model of coupled phase oscillators and perform three minimally cognitive evolutionary robotics experiments. The analyses focus both on a behavioural level description, investigating the robot’s trajectories, and on a mechanism level description, exploring the variables’ dynamics and the information transfer properties within and between the agent’s body and the environment. The first experiment demonstrates that in an active categorical perception task under normal and inverted vision, networks with a definite, but not too strong, propensity for synchronisation are more able to reconfigure, to organise themselves functionally, and to adapt to different behavioural conditions. The second experiment relates assembly constitution and phase reorganisation dynamics to performance in supervised and unsupervised learning tasks. We demonstrate that assembly dynamics facilitate the evolutionary process, can account for varying degrees of stimuli modulation of the sensorimotor interactions, and can contribute to solving different tasks leaving aside other plasticity mechanisms. The third experiment explores an associative learning task considering a more realistic connectivity pattern between neurons. We demonstrate that networks with travelling waves as a default solution perform poorly compared to networks that are normally synchronised in the absence of stimuli. Overall, this thesis shows that neural synchronisation dynamics, when suitably flexible and reconfigurable, produce an asymmetric flow of information and can generate minimally cognitive embodied behaviours

Breakdown of category-specific word representations in a brain-constrained neurocomputational model of semantic dementia

The neurobiological nature of semantic knowledge, i.e., the encoding and storage of conceptual information in the human brain, remains a poorly understood and hotly debated subject. Clinical data on semantic deficits and neuroimaging evidence from healthy individuals have suggested multiple cortical regions to be involved in the processing of meaning. These include semantic hubs (most notably, anterior temporal lobe, ATL) that take part in semantic processing in general as well as sensorimotor areas that process specific aspects/categories according to their modality. Biologically inspired neurocomputational models can help elucidate the exact roles of these regions in the functioning of the semantic system and, importantly, in its breakdown in neurological deficits. We used a neuroanatomically constrained computational model of frontotemporal cortices implicated in word acquisition and processing, and adapted it to simulate and explain the effects of semantic dementia (SD) on word processing abilities. SD is a devastating, yet insufficiently understood progressive neurodegenerative disease, characterised by semantic knowledge deterioration that is hypothesised to be specifically related to neural damage in the ATL. The behaviour of our brain-based model is in full accordance with clinical data—namely, word comprehension performance decreases as SD lesions in ATL progress, whereas word repetition abilities remain less affected. Furthermore, our model makes predictions about lesion- and category-specific effects of SD: our simulation results indicate that word processing should be more impaired for object- than for action-related words, and that degradation of white matter should produce more severe consequences than the same proportion of grey matter decay. In sum, the present results provide a neuromechanistic explanatory account of cortical-level language impairments observed during the onset and progress of semantic dementia

Memory capacity in the hippocampus

Neural assemblies in hippocampus encode positions. During rest, the hippocam- pus replays sequences of neural activity seen during awake behavior. This replay is linked to memory consolidation and mental exploration of the environment. Re- current networks can be used to model the replay of sequential activity. Multiple sequences can be stored in the synaptic connections. To achieve a high mem- ory capacity, recurrent networks require a pattern separation mechanism. Such a mechanism is global remapping, observed in place cell populations. A place cell fires at a particular position of an environment and is silent elsewhere. Multiple place cells usually cover an environment with their firing fields. Small changes in the environment or context of a behavioral task can cause global remapping, i.e. profound changes in place cell firing fields. Global remapping causes some cells to cease firing, other silent cells to gain a place field, and other place cells to move their firing field and change their peak firing rate. The effect is strong enough to make global remapping a viable pattern separation mechanism. We model two mechanisms that improve the memory capacity of recurrent net- works. The effect of inhibition on replay in a recurrent network is modeled using binary neurons and binary synapses. A mean field approximation is used to de- termine the optimal parameters for the inhibitory neuron population. Numerical simulations of the full model were carried out to verify the predictions of the mean field model. A second model analyzes a hypothesized global remapping mecha- nism, in which grid cell firing is used as feed forward input to place cells. Grid cells have multiple firing fields in the same environment, arranged in a hexagonal grid. Grid cells can be used in a model as feed forward inputs to place cells to produce place fields. In these grid-to-place cell models, shifts in the grid cell firing patterns cause remapping in the place cell population. We analyze the capacity of such a system to create sets of separated patterns, i.e. how many different spatial codes can be generated. The limiting factor are the synapses connecting grid cells to place cells. To assess their capacity, we produce different place codes in place and grid cell populations, by shuffling place field positions and shifting grid fields of grid cells. Then we use Hebbian learning to increase the synaptic weights be- tween grid and place cells for each set of grid and place code. The capacity limit is reached when synaptic interference makes it impossible to produce a place code with sufficient spatial acuity from grid cell firing. Additionally, it is desired to also maintain the place fields compact, or sparse if seen from a coding standpoint. Of course, as more environments are stored, the sparseness is lost. Interestingly, place cells lose the sparseness of their firing fields much earlier than their spatial acuity. For the sequence replay model we are able to increase capacity in a simulated recurrent network by including an inhibitory population. We show that even in this more complicated case, capacity is improved. We observe oscillations in the average activity of both excitatory and inhibitory neuron populations. The oscillations get stronger at the capacity limit. In addition, at the capacity limit, rather than observing a sudden failure of replay, we find sequences are replayed transiently for a couple of time steps before failing. Analyzing the remapping model, we find that, as we store more spatial codes in the synapses, first the sparseness of place fields is lost. Only later do we observe a decay in spatial acuity of the code. We found two ways to maintain sparse place fields while achieving a high capacity: inhibition between place cells, and partitioning the place cell population so that learning affects only a small fraction of them in each environment. We present scaling predictions that suggest that hundreds of thousands of spatial codes can be produced by this pattern separation mechanism. The effect inhibition has on the replay model is two-fold. Capacity is increased, and the graceful transition from full replay to failure allows for higher capacities when using short sequences. Additional mechanisms not explored in this model could be at work to concatenate these short sequences, or could perform more complex operations on them. The interplay of excitatory and inhibitory populations gives rise to oscillations, which are strongest at the capacity limit. The oscillation draws a picture of how a memory mechanism can cause hippocampal oscillations as observed in experiments. In the remapping model we showed that sparseness of place cell firing is constraining the capacity of this pattern separation mechanism. Grid codes outperform place codes regarding spatial acuity, as shown in Mathis et al. (2012). Our model shows that the grid-to-place transformation is not harnessing the full spatial information from the grid code in order to maintain sparse place fields. This suggests that the two codes are independent, and communication between the areas might be mostly for synchronization. High spatial acuity seems to be a specialization of the grid code, while the place code is more suitable for memory tasks. In a detailed model of hippocampal replay we show that feedback inhibition can increase the number of sequences that can be replayed. The effect of inhibition on capacity is determined using a meanfield model, and the results are verified with numerical simulations of the full network. Transient replay is found at the capacity limit, accompanied by oscillations that resemble sharp wave ripples in hippocampus. In a second model Hippocampal replay of neuronal activity is linked to memory consolidation and mental exploration. Furthermore, replay is a potential neural correlate of episodic memory. To model hippocampal sequence replay, recurrent neural networks are used. Memory capacity of such networks is of great interest to determine their biological feasibility. And additionally, any mechanism that improves capacity has explanatory power. We investigate two such mechanisms. The first mechanism to improve capacity is global, unspecific feedback inhibition for the recurrent network. In a simplified meanfield model we show that capacity is indeed improved. The second mechanism that increases memory capacity is pattern separation. In the spatial context of hippocampal place cell firing, global remapping is one way to achieve pattern separation. Changes in the environment or context of a task cause global remapping. During global remapping, place cell firing changes in unpredictable ways: cells shift their place fields, or fully cease firing, and formerly silent cells acquire place fields. Global remapping can be triggered by subtle changes in grid cells that give feed-forward inputs to hippocampal place cells. We investigate the capacity of the underlying synaptic connections, defined as the number of different environments that can be represented at a given spatial acuity. We find two essential conditions to achieve a high capacity and sparse place fields: inhibition between place cells, and partitioning the place cell population so that learning affects only a small fraction of them in each environments. We also find that sparsity of place fields is the constraining factor of the model rather than spatial acuity. Since the hippocampal place code is sparse, we conclude that the hippocampus does not fully harness the spatial information available in the grid code. The two codes of space might thus serve different purposes