In this article, the authors consider optimal decision making in two-alternative forced-choice (TAFC) tasks. They begin by analyzing 6 models of TAFC decision making and show that all but one can be reduced to the drift diffusion model, implementing the statistically optimal algorithm (most accurate for a given speed or fastest for a given accuracy). They prove further that there is always an optimal trade-off between speed and accuracy that maximizes various reward functions, including reward rate (percentage of correct responses per unit time), as well as several other objective functions, including ones weighted for accuracy. They use these findings to address empirical data and make novel predictions about performance under optimality.

We undertake a probabilistic analysis of the response of repetitively firing neural populations to simple pulselike stimuli. Recalling and extending results from the literature, we compute phase response curves (PRCs) valid near bifurcations to periodic firing for Hindmarsh-Rose, Hodgkin-Huxley, FitzHugh-Nagumo, and Morris-Lecar models, encompassing the four generic (codimension one) bifurcations. Phase density equations are then used to analyze the role of the bifurcation, and the resulting PRC, in responses to stimuli. In particular, we explore the interplay among stimulus duration, baseline firing frequency, and population-level response patterns. We interpret the results in terms of the signal processing measure of gain and discuss further applications and experimentally testable predictions.

In choice reaction time tasks, response times and error rates demonstrate differential dependencies on the identities of up to four stimuli preceding the current one. Although the general profile of reaction times and error rates, when plotted against the stimulus histories, may seem idiosyncratic, we show that it can result from simple underlying mechanisms that take account of the occurrence of stimulus repetitions and alternations. Employing a simple connectionist model of a two-alternative forcedchoice task, we explored various combinations of repetition and alternation detection schemes in an attempt to account for empirical results from the literature and from our own studies. We found that certain combinations of the repetition and the alternation schemes provided good fits to the data, suggesting that simple mechanisms may serve to explain the complicated but highly reproducible higher order dependencies of task performance on stimulus history.

We review simple connectionist and firing rate models for mutually inhibiting pools of neurons that discriminate between pairs of stimuli. Both are two-dimensional nonlinear stochastic ordinary differential equations, and although they differ in how inputs and stimuli enter, we show that they are equivalent under state variable and parameter coordinate changes. A key parameter is gain: the maximum slope of the sigmoidal activation function. We develop piecewise-linear and purely linear models, and one-dimensional reductions to Ornstein–Uhlenbeck processes that can be viewed as linear filters, and show that reaction time and error rate statistics are well approximated by these simpler models. We then pose and solve the optimal gain problem for the Ornstein–Uhlenbeck processes, finding explicit gain schedules that minimize error rates for time-varying stimuli. We relate these to time courses of norepinephrine release in cortical areas, and argue that transient firing rate changes in the brainstem nucleus locus coeruleus may be responsible for approximate gain optimization.

We describe the dynamical and bifurcational behavior of two mutually inhibitory, leaky, neural units subject to external stimulus, random noise, and "priming biases". The model describes a simple forced choice experiment and accounts for varying levels of expectation and control. By projecting the model's dynamics onto slow manifolds, using judicious linear approximations, and solving for one-dimensional (reduced) probability densities, analytical estimates are developed for reaction time distributions and shown to compare satisfactorily with "full" numerical data. A sensitivity analysis is performed and the effects of parameters assessed. The predictions are also compared with behavioral data. These results may help correlate low-dimensional models of stochastic neural networks with cognitive test data, and hence assist in parameter choices and model building.

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We model spiking neurons in locus coeruleus (LC), a brain nucleus involved in modulating cognitive performance, and compare with recent experimental data. Extracellular recordings from LC of monkeys performing target detection and selective attention tasks show varying responses dependent on stimuli and performance accuracy. From membrane voltage and ion channel equations, we derive a phase oscillator model for LC neurons. Average spiking probabilities of a pool of cells over many trials are then computed via a probability density formulation. These show that: (1) Post-stimulus response is elevated in populations with lower spike rates; (2) Responses decay exponentially due to noise and variable pre-stimulus spike rates; and (3) Shorter stimuli preferentially cause depressed post-activation spiking. These results allow us to propose mechanisms for the different LC responses observed across behavioral and task conditions, and to make explicit the role of baseline firing rates and the duration of task-related inputs in determining LC response.

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