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Review
. 2017 Feb 19;373(1740):20170043.
doi: 10.1098/rstb.2017.0043.

An emergentist perspective on the origin of number sense

Affiliations
Review

An emergentist perspective on the origin of number sense

Marco Zorzi et al. Philos Trans R Soc Lond B Biol Sci. .

Abstract

The finding that human infants and many other animal species are sensitive to numerical quantity has been widely interpreted as evidence for evolved, biologically determined numerical capacities across unrelated species, thereby supporting a 'nativist' stance on the origin of number sense. Here, we tackle this issue within the 'emergentist' perspective provided by artificial neural network models, and we build on computer simulations to discuss two different approaches to think about the innateness of number sense. The first, illustrated by artificial life simulations, shows that numerical abilities can be supported by domain-specific representations emerging from evolutionary pressure. The second assumes that numerical representations need not be genetically pre-determined but can emerge from the interplay between innate architectural constraints and domain-general learning mechanisms, instantiated in deep learning simulations. We show that deep neural networks endowed with basic visuospatial processing exhibit a remarkable performance in numerosity discrimination before any experience-dependent learning, whereas unsupervised sensory experience with visual sets leads to subsequent improvement of number acuity and reduces the influence of continuous visual cues. The emergent neuronal code for numbers in the model includes both numerosity-sensitive (summation coding) and numerosity-selective response profiles, closely mirroring those found in monkey intraparietal neurons. We conclude that a form of innatism based on architectural and learning biases is a fruitful approach to understanding the origin and development of number sense.This article is part of a discussion meeting issue 'The origins of numerical abilities'.

Keywords: artificial neural networks; computational modelling; deep learning; number sense; numerical development; numerosity perception.

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Conflict of interest statement

We declare we have no competing interests.

Figures

Figure 1.
Figure 1.
(a) Representation of an agent (black triangle) within a section of its artificial ecosystem. In the left panel, the agent is facing right and can sense food (grey circles) in its right and left sensor fields. The right panel shows the same agent after making a single turn to the left: it can now sense only one cell containing food. (b) Schematic representation of the recurrent architecture controlling each agent. The sensory layer receives information from the four cells in the agent's field of view, with food quantity in each cell encoded by nine binary neurons. The effector neurons in the motor layer define which action is chosen at each time-step. (c) Test trial, where the agent must select between two food sources encoding different numerosities. (d) Mean accuracy (left panel) and response time (RT, right panel) as a function of the numerical distance between food quantities. (e) Examples of numerosity-sensitive hidden neurons showing monotonically increasing or decreasing response profiles (i.e. summation coding). All panels have been adapted from [40].
Figure 2.
Figure 2.
(a) Schematic representation of the deep learning model. Stimuli are provided through an input layer, and activation is then propagated through a first hidden layer encoding a set of simple spatial filters (hard-wired connections) and a second hidden layer encoding numerosity information (connections adjusted through unsupervised learning). These internal representations are finally read-out by a response layer to simulate the numerosity comparison task. (b) Receptive fields of the spatial filters (on- and off-centre detectors) used in the first hidden layer. Strong, negative connections are represented in black, while strong, excitatory connections are represented in white. Grey colour indicates that connection weight is around zero. A 3D representation of two prototypical off- and on-centre detectors is reported at the bottom.
Figure 3.
Figure 3.
(a) Learning trajectory of the model, corresponding to the estimated Weber fraction after every 30 learning epochs. (b) Accuracy of the model in the number comparison task as a function of numerical ratio (chance level is at 0.5) when only 25% of the stimuli were used for task learning (supervised training). Performance of the initial network (random) is compared with that of the network following unsupervised learning (mature). (c) Performance of the initial network when only 1% of the stimuli were used for task learning. (Online version in colour.)
Figure 4.
Figure 4.
(a) Examples of congruent and incongruent stimulus pairs correctly classified by the read-out layer of the initial (random) network. (b) Accuracy of initial and mature networks on congruent and incongruent trials (numerical ratio is 1 : 2). (c) Cost of incongruency (performance difference between incongruent and congruent trials) for the initial and mature networks as a function of numerical ratio.
Figure 5.
Figure 5.
(a) Summation coding in the model. The first two scatter plots represent the distribution of numerosity and cumulative area regression coefficients (B) for the initial (random) network and for the trained (mature) network, respectively. The bottom panel shows the count of increasing (positive slope) and decreasing (negative slope) numerosity detectors. (b) Numerosity-selective coding in the model compared with neurons in monkey ventral intraparietal area (VIP; neurophysiological data from [81], reproduced with permission). First row: normalized responses averaged for neurons preferring the same numerosity. Second row: response profiles plotted against the numerical distance from the preferred numerosity. Third row: frequency distributions of preferred numerosity in the population of numerosity-selective neurons.

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