Abstract
Humans typically make nearoptimal sensorimotor judgements but show systematic biases when making more cognitive judgements. Here we test the hypothesis that, while humans are sensitive to the noise present during early sensory encoding, the “optimality gap” arises because they are blind to noise introduced by later cognitive integration of variable or discordant pieces of information. In six psychophysical experiments, human observers judged the average orientation of an array of contrast gratings. We varied the stimulus contrast (encoding noise) and orientation variability (integration noise) of the array. Participants adapted nearoptimally to changes in encoding noise, but, under increased integration noise, displayed a range of suboptimal behaviours: they ignored stimulus base rates, reported excessive confidence in their choices, and refrained from opting out of objectively difficult trials. These overconfident behaviours were captured by a Bayesian model blind to integration noise. Our study provides a computationally grounded explanation of human suboptimal cognitive inference.
Introduction
The question of whether humans make optimal choices has received considerable attention in the neural, cognitive and behavioural sciences. On the one hand, the general consensus in sensory psychophysics and sensorimotor neuroscience is that choices are nearoptimal. For example, humans have been shown to combine different sources of stimulus information in a statistically nearoptimal manner, weighting each source by its reliability^{1,2,3,4,5,6}. Humans have also been shown to nearoptimally utilise knowledge about stimulus base rates to resolve stimulus ambiguity^{7,8,9,10,11}.
On the other hand, psychologists and behavioural economists, studying more cognitive judgements, have argued that human choices are suboptimal^{12}. For example, when required to guess a person’s occupation, humans neglect the base rate of different professions and solely rely on the person’s description provided by the experimenter. Such suboptimality has been attributed to insufficient past experience^{13}, limited stakes in laboratory settings^{14}, the format in which problems are posed^{15}, distortions in representations of values and probabilities^{16}, and/or a reluctance to employ costly cognitive resources^{17,18}. However, an account of human decisionmaking that can explain both perceptual optimality and cognitive suboptimality has yet to emerge^{19}.
Here we propose that resolving this apparent paradox requires recognizing that perceptual and cognitive choices often are corrupted by different sources of noise. More specifically, choices in perceptual and cognitive tasks tend to be corrupted by noise that arises at different stages of the information processing leading up to a choice^{20,21,22,23}. In perceptual tasks, experimenters typically manipulate noise arising before or during sensory encoding. For example, they may vary the contrast of a grating, or the net motion energy in a random dot kinematogram, which affects the signaltonoise ratio of the encoded stimulus and in turn the sensory percept^{24}. Conversely, in cognitive tasks, which often involve written materials or clearly perceptible stimuli, experimenters typically seek to manipulate noise arising after stimulus encoding. For example, they may vary the discrepancy between different pieces of information bearing on a choice, such as the relative costs and benefits of a consumer product^{18}. These types of judgement are difficult because they require integration of multiple, sometimes highly discordant, pieces of information within a limitedcapacity cognitive system^{25,26,27}.
Here we test the hypothesis that, while humans are sensitive to noise arising during early sensory encoding, they are blind to the additional noise introduced by their own cognitive system when integrating variable pieces of information. We tested this hypothesis using a novel psychophysical paradigm that separates, within a single task, these two types of noise. In particular, observers were asked to categorise the average tilt of an array of gratings. We manipulated encoding noise (i.e. the perceptual difficulty of encoding an individual piece of information) by changing the contrast of the array of gratings, with decisions being harder for lowcontrast arrays. Second, we manipulated integration noise (i.e. the cognitive difficulty of integrating multiple pieces of information) by changing the variability of the orientations of individual gratings, with decisions being harder for highvariability arrays. Manipulating these different sources of noise within a single task allows us to rule out previous explanations of the optimality gap which hinge on task differences. To preempt our results, we show that, while observers adapt nearoptimally to increases in encoding noise, they fail to adapt to increases in integration noise. We argue that such noise blindness is a major driver of suboptimal cognitive inference and may explain the gap in optimality between perceptual and cognitive judgements.
Results
Experimental dissociation of encoding and integration noise
All six experiments were based on the same psychophysical task (see Methods). On each trial, participants were presented with eight tilted gratings organized in a circular array. Participants were required to categorise the average orientation of the array as oriented clockwise (CW) or counterclockwise (CCW) relative to the horizontal axis (Fig. 1a, b). After having made a response, participants received categorical feedback about choice accuracy, before continuing to the next trial. We manipulated two features of the stimulus array to dissociate encoding noise and integration noise: the contrast of the gratings (root mean square contrast, rmc: {0.15, 0.6}), which affects encoding noise, and the variability of the gratings’ orientations (standard deviation of orientations, std: {0°, 4°, 10°}), which affects integration noise. The underlying distribution of average orientations was identical for all experimental conditions.
In Experiments 1 (n = 20) and 2 (n = 20), we assessed the effects of contrast and variability on choice accuracy and evaluated participants’ awareness of these effects. In both experiments, at the beginning of a trial, we provided a prior cue which, on half of the trials, signalled the correct stimulus category with 75% probability (henceforth biased trials), and, on the other half of trials, provided no information about the stimulus category (henceforth neutral trials) (Fig. 1b). The neutral trials provided us with a baseline measure of participants’ choice accuracy in the different conditions of our factorial design, and the biased trials allowed us to assess the degree to which—if at all—participants compensated for reduced choice accuracy in a given experimental condition by relying more on the prior cue. In Experiment 2, to provide additional insight into participants’ awareness of their own performance, we asked participants to report confidence in their choices (i.e. the probability that a choice is correct; Fig. 1c).
Matched performance under encoding and integration noise
We first used the neutral trials to benchmark the effects of contrast and variability on choice accuracy. As intended, choice accuracy decreased with lower contrast (ANOVAs; Exp1: F(1,19) = 15.5, p < 0.001; Exp2: F(1,19) = 40.7, p < 0.001; collapsed: F(1,39) = 49.1, p < 0.001) and with higher variability (ANOVAs; Exp1: F(1.2,24.5) = 8.4, p < 0.01; Exp2: F(1.6,32.0) = 26.4, p < 0.001; collapsed: F(1.4,56.9) = 30.6, p < 0.001). Our factorial design contained three critical conditions which allowed us to compare participants’ behaviour under distinct sources of noise: (i) baseline, (ii) lowc and (iii) highv. In the baseline condition, the total amount of noise is lowest (high contrast, 0.6; zero variability, 0°). In the lowc condition (low contrast, 0.15; zero variability, 0°), encoding noise is high but integration noise is low. Conversely, in the highv condition, integration noise is high but encoding noise is low (high contrast, 0.6; high variability, 10°). As expected, choice accuracy was reduced both in the lowc and in the highv conditions (about 12%) compared to the baseline condition (ttests; baseline > lowc: t(39) = 9.24, p < 0.001; baseline > highv: t(39) = 9.69, p < 0.001; Fig. 2a). Critically, choice accuracy was at statistically similar levels in the lowc and the highv conditions (ttests; Exp1, highv > lowc: t(19) = 0.09, p > 0.9; Exp2, highv > lowc: t(19) = 0.31, p > 0.7; collapsed, highv > lowc: t(39) = 0.28, p > 0.7; Fig. 2a). Overall, the results show that we successfully manipulated noise at different stages of information processing.
Cue usage under encoding and integration noise
We next leveraged the biased trials to assess the degree to which participants adapted to the changes in choice accuracy induced by our factorial design. Given the above results, we would expect participants to rely more on the prior cue in the lowc and the highv condition than in the baseline condition. To test this prediction, we applied signal detection theory^{28,29} to quantify the degree to which participants shifted their decision criterion in accordance with the prior cue (see Methods). Briefly, we constructed a bias index, which was computed as the difference in the decision criteria between the condition where the prior cue was clockwise and the condition where the prior cue was counterclockwise. The higher the bias index, the higher the influence of the prior cue on choice.
As expected under an ideal observer framework, participants used the prior cue more in the lowc than in the baseline condition (ttest; t(39) = 4.89, p < 0.001; Fig. 2c). However, contrary to an ideal observer framework, participants used the prior cue less in the highv than in the baseline condition (ttest; t(39) = 2.85, p < 0.01; Fig. 2c). This pattern is clear from psychometric curves created separately for each condition (compare inflection points in Fig. 2b). Consistent with these results, a full factorial analysis of the bias index identified a negative main effect of contrast (ANOVA; F(1,39) = 24.5, p < 0.001) and a negative main effect of variability (ANOVA; F(1.9,75.7) = 10.0, p < 0.001; Fig. 2d). Finally, including both neutral and biased trials, we used trialbytrial logistic regression to investigate how contrast (c) and variability (v) affected the influence of the prior cue and sensory evidence (μθ) on choices (μθ, cue, μθ*c, μθ*v, cue*c, cue*v; Fig. 2e). The prior cue had a larger influence on choices on lowcontrast compared to highcontrast trials (ttest; t(39) = 4.05, p < 0.001) and on lowvariability compared to highvariability trials (ttest; t(39) = 5.21, p < 0.001). Taken together, these results show that participants did not adapt to the additional noise arising during integration of variable pieces of information.
Overconfidence under integration noise
To test whether participants did not adapt because they were blind to integration noise, we analysed the confidence reports elicited in Experiment 2 (Fig. 1c). We implemented a strictly proper scoring rule such that it was in participants’ best interest (i) to make as many accurate choices as possible and (ii) to estimate the probability that a choice is correct as accurately as possible^{30}. In support of our hypothesis, analysis of the full factorial design showed that, while mean confidence (we did not analyse other statistical moments) varied with contrast (ANOVA; F(1,19) = 32.9, p < 0.001), it did not vary with variability (ANOVA; F(1.1,22.7) = 0.64, p > 0.5). In addition, direct comparison between the lowc and highv conditions showed that participants were more confident in the highv condition (ttest; t(19) = 3.97, p < 0.001; Fig. 3a), with participants overestimating their performance (difference between mean confidence and mean accuracy in the highv condition, ttest; t(19) = 5.60, p < 0.001; greater overconfidence in the highv than in the lowc condition, ttest; t(19) = 2.70, p < 0.05; Fig. 3c). Although participants reported lower confidence in the highv condition compared to baseline (Fig. 3a), this decrease was due to participants utilising response times (RTs) as a cue to confidence^{31}: a trialbytrial regression analysis showed that confidence decreased with longer RTs and was unaffected by variability once RTs had been accounted for (ttests; v, t(19) = 0.38, p > 0.7; other predictors, all tvalues > 4, all p < 0.001; see Fig. 3b, see Supplementary Note 7 and Supplementary Fig. 7 for a discussion between RTs and confidence).
In Experiment 3 (n = 18), because explicit confidence reports can be highly idiosyncratic^{32,33,34}, we obtained an implicit, but perhaps more direct measure of confidence (Fig. 1d)^{35,36,37}. Specifically, on half of the trials (optional trials), we introduced an additional choice option, an optout option, which yielded “correct” feedback with a 75% probability. On the other half of trials (forced trials), participants had to make an orientation judgement. Under this design, to maximise reward, participants should choose the optout option whenever they thought they were less than 75% likely to make a correct choice. Despite matched levels of choice accuracy in the lowc and the highv conditions (ttest; forced trials, t(17) = 0.26, p > 0.7), participants decided to make an orientation judgement more often on highv than on lowc trials (ttest; optional trials, t(17) = 2.35, p < 0.05; Fig. 3d), again indicating overconfidence in the face of integration noise. A full factorial analysis verified that the proportion of such optin trials varied with contrast (ANOVA; F(1,17) = 21.3, p < 0.001) but not with variability (ANOVA; F(1.4,24.0) = 3.5, p > 0.05). Similarly, a trialbytrial logistic regression showed that the probability of opting in varied with contrast (ttest; t(17) = 6.93, p < 0.001) but not with variability (ttest; t(17) = 1.6, p > 0.1), after controlling for other taskrelevant factors. Overall, participants’ confidence (probed explicitly or implicitly) was lower when encoding noise was high, but not so when integration noise was high, despite making a comparable proportion of errors in the two conditions. These results indicate that participants were blind to integration noise.
Computational model of noise blindness
We next compared a set of computational models based on an ideal observer framework to provide a mechanistic explanation of the observed data (see Methods and Supplementary Table 1 for an overview of all models considered). There are broadly three components to our approach. First, a generative (true) model which describes the task structure and how noisy sensory evidence is generated. Second, an agent’s internal model of the task structure and how sensory evidence is generated. Critically, the internal model may differ from the generative model. Third, a Bayesian inference process which involves inverting the internal model in order to estimate the probability of a stimulus category given sensory evidence and in turn make a response. This process involves marginalising over contrast and variability levels according to a belief distribution over the different experimental conditions. Optimal behaviour can be said to occur when there is a direct correspondence between the generative model and the agent’s internal model. We evaluated the models both qualitatively (i.e. model predictions for critical experimental conditions) and quantitatively (i.e. BIC scores).
We focus here on an omniscient model, which has perfect knowledge of the task structure and how sensory evidence is generated, and two suboptimal models, which provide different accounts of participants’ lack of sensitivity to the performance cost associated with stimulus variability. The suboptimal models relax the omniscient assumptions about an agent’s beliefs about (i) the task structure and/or (ii) the sources of noise in play.
In our task, the distribution of average orientations was common across experimental conditions and consequently independent of contrast and variability (Fig. 4a). We therefore modelled an agent’s sensory evidence as a random (noisy) sample from a Gaussian distribution centred on the average orientation of the stimulus array (Fig. 4b), with the variance of this distribution determined by both encoding noise and integration noise. We verified that the results reported below are not due to this simplifying assumption (see Supplementary Note 2 and Supplementary Fig. 2 where we simulate data under a Bayesian model which operates with eight noisy samples, one for the orientation of each grating, rather than one noisy sample). We used each participant’s data from the neutral trials to parameterise their levels of encoding noise and integration noise in each experimental condition (see Methods). The fitted noise levels, which are part of the generative model, were the same for all models; no additional free parameters were fitted to the data and the models only differed with respect to their assumptions about the internal model.
The omniscient model has, for each experimental condition, a pair of functions that specify the probability density over sensory evidence given a CW and a CCW stimulus, taking into account both encoding and integration noise. As the model can identify the current condition (e.g., knows with certainty that a trial is drawn from the highcontrast, highvariability condition), it only uses the relevant pair of density functions to compute the probability of the observed sensory evidence given a CCW and a CW category (Fig. 4c). On neutral trials, each category is equally likely, and the agent computes the probability that a stimulus is CW and CCW directly from the density functions. On biased trials, the categories have different prior probabilities, and the agent scales the density functions by the prior probability of each category as indicated by the prior cue (Fig. 4d). After having calculated the probability that a stimulus is CW and CCW, the agent can compute a choice (i.e. chose the category with the higher posterior probability) and confidence in this choice (i.e. the probability that the choice is correct).
We now consider two alternative explanations of the participants’ lack of sensitivity to the performance cost associated with stimulus variability. First, a variabilitymixer model which relaxes the assumption that an agent can identify the current variability condition. Specifically, the model uses a single pair of density functions for all variability conditions (i.e. a mixture of density functions across variability conditions). As a result, compared to the omniscient model, the density functions are wider on lowvariability trials but narrower on highvariability trials. Second, a noiseblind model which relaxes the assumption that the agent is aware of integration noise. As for the variabilitymixer model, the noiseblind model uses a single pair of density functions for all variability conditions, but, critically, these density functions do not reflect the additional noise due to stimulus variability. Because of these differences in the internal model used for Bayesian inference, the three models differ in the degree of confidence in a choice for a given sensory evidence (Fig. 4f) and, by extension, the influence of the prior cue on choice on biased trials.
In support of our hypothesis, the noiseblind model provided the best fit to our data. First, the noiseblind model, and not the omniscient model, predicted three key features of participants’ behaviour: (i) overconfidence on highvariability trials within participants (Supplementary Note 3 and Supplementary Fig. 3), (ii) no correlation between mean accuracy and mean confidence across participants on highvariability trials (Fig. 5a), and (iii) a diminished influence of the prior cue on highvariability trials, as revealed by both the bias index (Fig. 5c) and the trialbytrial regression predicting (signed) confidence (Fig. 5d), where the prior cue has a positive effect on confidence but less so when variability is high. Second, quantitative comparison yielded “very strong evidence”^{38} for the noiseblind model over the omniscient model, with an average ΔBIC across participants of −32.9 (Fig. 5b). Finally, analyses of the patterns of overconfidence in the critical conditions of our factorial design favoured the noiseblind over the variabilitymixer model (Supplementary Fig. 3), and quantitative comparison yielded “very strong evidence” for the noiseblind over the variabilitymixer model (ΔBIC = −20.4, Fig. 5b). In summary, the modelling indicates that participants neglected integration noise altogether.
Participants are noise blind and not variability blind
To further rule out the hypothesis that participants were simply unable to discriminate the variability conditions as proposed by the variabilitymixer model, we ran Experiment 4 (n = 23). After having made a choice, participants were asked to categorise either the contrast of the stimulus array (rmc, high: 0.6 vs. low: 0.15) or the variability of the stimulus array (std, high: 10° vs. low: 0°) (Fig. 1e). Again, choice accuracy on neutral trials in the lowc and the highv conditions was statistically indistinguishable (ttest; t(22) = 1.22, p > 0.2). We reasoned that, if participants had difficulty identifying the variability condition but were otherwise aware of integration noise, then they should behave closer to optimal when they correctly identified the variability condition. To test this prediction, we used the biased trials to compare cue usage when the variability condition was correctly and incorrectly categorised (75.71 ± 2.26% of the variability judgements were correct). In contrast to the prediction, but in line with our hypothesis, participants showed blindness to integration noise even when they correctly identified the variability condition: participants were more biased on lowc than highv trials regardless of whether the variability categorisation was correct (ttest; t(22) = 3.03, p < 0.01) or incorrect (ttest; t(22) = 2.96, p < 0.01; Fig. 6a, b).
In Experiments 1–4, the experimental conditions were interleaved across trials, which may have made it too difficult for participants to separate the different sources of noise in play. To further test the generality of our results, we ran Experiment 5 (n = 24) in which either the contrast or the variability level was kept constant across a block of trials (Fig. 6c, d). Even then, and despite receiving trialbytrial feedback, participants were not more influenced by the prior cue when variability was high compared to the baseline condition (ttest; biased trials, t(23) = 0.80, p > 0.4), but they were more influenced by the prior cue when contrast was low than when variability was high (ttest; biased trials, t(23) = 2.37, p < 0.05).
Sequential sampling account of noise blindness
A recent study investigated how stimulus volatility (i.e. changes in evidence intensity within a trial) affected choice and confidence^{39}. Participants were found to make faster responses and report higher confidence when stimulus volatility was high. These results were explained by a sequential sampling model which assumes that observers are unaware of stimulus volatility and therefore, unlike an omniscient model, adopt a common choice threshold across trial types. We show, using empirical and computational analyses, that this model cannot explain our results (Supplementary Note 4 and Supplementary Fig. 4). For example, the model predicts faster RTs on highvariability than lowvariability trials, a prediction which is at odds with our observation of slower RTs on highvariability trials. To further evaluate how our experimental manipulations affected the choice process, we fitted a hierarchical instantiation of the driftdiffusion model^{40} to participants’ choice behaviour on neutral trials. In line with the above results, this analysis showed that the effects of contrast and variability on accuracy and RTs were captured by a change in driftrate and not in threshold or nondecision time (Supplementary Note 5 and Supplementary Fig. 5).
Noise blindness cannot be explained by subsampling
We have proposed that stimulus variability impairs performance because of noise inherent to cognitive integration of variable pieces of information. An alternative explanation of the performance cost for high stimulus variability is that participants based their responses on a subset of gratings rather than the full array. Under this subsampling account, choice accuracy for highvariability stimuli is lower because of a larger mismatch between the average orientation of the full array and the average orientation of the sampled subset. Here we provide several lines of evidence against the subsampling account (also Supplementary Note 6 and Supplementary Fig. 6).
We first examined performance under different setsizes in Experiment 6 (n = 20) where the stimulus array was made up of either four or eight gratings (average orientations and orientation variability were equated across setsizes). We reasoned that, if participants did indeed engage in subsampling, then performance should be higher for four than eight gratings: sampling four items should impair performance in the highv condition for an eightitem array but not for a fouritem array because the average orientations were matched across experimental conditions. However, in contrast to the subsampling account, we found no effect of setsize on choice accuracy (ANOVA; F(1,20) = 0.004, p > 0.9; Supplementary Fig. 6a), with the effects of contrast (ANOVA; F(1,20) = 39.6, p < 0.001) and variability (ANOVA; F(1,20) = 30.3, p < 0.001) comparable to those observed in the previous experiments.
We next simulated performance for eightgrating arrays under a subsampling agent which did not have integration noise but instead sampled a subset of the items (1–8 items, Supplementary Fig. 6b). The observed difference in participants’ performance between the baseline and the highv conditions could be explained by assuming an agent that sampled about four items out of eight. However, this account—because there is no integration noise—predicts that participants should have similar levels of performance for the baseline and the highv conditions for fouritem arrays, a prediction which is at odds with our data (Supplementary Fig. 6a). If integration noise is introduced, then most, if not all, items would have to be sampled to account for the data.
Finally, we fitted a computational model to participants’ choices in Experiments 1 to 3 (eightitem arrays) in order to directly estimate the number of items sampled by each participant. This modelling approach revealed that the majority of participants (42 out of 60) sampled all eight items (Supplementary Table 2). We emphasise that subsampling, even if an auxiliary cause of integration noise, cannot by itself explain participants’ lack of sensitivity to the performance cost associated with highvariability stimuli.
Discussion
Here we propose a new explanation for the previously reported gap in optimality between perceptual and cognitive decisions. Using a novel paradigm, we show, within a single task, that humans are sensitive to noise present during sensory encoding, in keeping with previous perceptual studies^{1,8}, but blind to noise arising when having to integrate variable or discordant pieces of information, often a requirement in cognitive tasks. This noise blindness gave rise to two common signatures of suboptimality found in cognitive studies: baserate neglect and overconfidence.
We provided several lines of evidence for our hypothesis. We showed that, when stimulus variability was high, participants were overconfident, as indicated by cue usage, confidence reports, and optin responses, even though they received trialbytrial feedback. We found overconfidence even when stimulus variability was salient (Exp1–3), accurately categorised (Exp4), or constant across a block of trials (Exp5). Overall, these lines of evidence indicate that, while participants were able to track stimulus variability, they simply neglected the performance cost associated with highvariability stimuli. Consistent with this interpretation, the bestfitting computational model of our data indeed assumed that participants were blind to the additional noise inherent to cognitive integration of variable pieces of information.
An extensive literature has considered the different types of noise which affect human choices^{21,22,41}. Our classification is partially related to a previous distinction between noise which originates inside the brain, such as intrinsic stochasticity in sensory transduction^{42}, and noise which arises outside the brain, such as a probabilistic relationship between a cue and a reward^{43}. Specifically, our account classifies noise according to when it arises during the information processing that precedes a choice. Encoding noise refers to noise accumulated up to the point at which a stimulus is encoded. As such, encoding noise includes both external noise (e.g., a weak correspondence between a retinal image in dim lighting and the object that caused the image) and internal noise (e.g., intrinsic stochasticity in sensory transduction). By comparison, integration noise strictly refers to internal noise which arises at later stages of information processing, when two or more pieces of information need to be integrated either in space or time, within a limitedcapacity cognitive system in order to make a choice. There are several potential contributors to such noise. For instance, errors of inference and information updating^{44}, information decay in working memory^{45}, temporal biases such as recency and primacy^{46}, and conflict among relevant information^{26,27}. Of course, choices may be affected by other types of noise than those considered here. For example, cognitive decisions may involve memories, sometimes distant in the past, and risk and ambiguity^{47,48}.
Many psychophysical tasks confound encoding and integration noise. For instance, in the classic random dotmotion task, decreasing motion coherence is typically thought to increase encoding noise, as momentary evidence is less indicative of the underlying motion direction^{49,50}. However, decreasing motion coherence can also affect integration noise, as momentary evidence becomes more variable relative to a running estimate of motion direction. Indeed, recent work has shown that noisy cognitive inference, related to our notion of integration noise, is a major driver of variability in choices^{51}. Similarly, it has been shown that for complex inference problems, a mismatch between an agent’s internal model of a task and the true structure of a task provokes departures from optimality^{41}. Here we extend these findings by introducing noise blindness as an additional driver of suboptimal cognitive inference. Choice variability due to integration noise, or imperfect inference, may not systematically bias choices away from the correct choice. Blindness to these sources of choice variability, however, predicts systematic overconfidence as reported in the current study. In short, we show that suboptimality can arise not only from having the wrong model of a task but also from having the wrong model of oneself.
We recognize that using our task alone it is hard to categorically say whether the locus of integration noise is early (e.g., in early sensory cortex) or late (e.g., higher association cortex where information is combined over broader windows in space and time). However, several lines of evidence indicate a late locus. First, participants can detect stimulus variability (Exp4), which we would not expect if the sensory representations themselves were distorted during early processing stages, and in support of a higherorder account, noise blindness does not depend on whether variability was accurately discriminated (Fig. 6a, b). Second, the effect of stimulus variability on participants’ choice accuracy does not depend on setsize (four vs. eight items in Exp6), and again in support of a higherorder account, neither did the observed noise blindness. Third, participants’ RTs and the driftdiffusion modelling suggest that information processing continues after stimulus offset and is thus unlikely to occur in early sensory areas. Fourth, stimulus variability is reflected in brain activity in higher association and control areas (e.g., parietal cortex, anterior insula, and dorsomedial prefrontal cortex)^{52}, which is consistent with integration noise arising after sensory encoding. More generally, our study is an example of the emerging use of perceptual tasks as a window onto general principles of cognition and decisionmaking^{53}.
We do not know why humans are blind to integration noise. One possibility is that basing decision strategies on all sources of noise would prolong deliberation and thus reduce reward rates, or that recognising one’s own cognitive deficiencies requires a much longer timeframe. However, a wellknown cognitive illusion may help understand why blindness to one’s own cognitive deficiencies may not be catastrophic: even though failures to detect salient visual change suggests that cognitive processing is highly limited^{54}, humans enjoy rich, vivid visual experiences of cluttered natural scenes. Human information processing is sharply limited by capacity, but as agents we may not need to be aware of the extent of these limitations.
Methods
Participants
One hundred and twentyeight healthy human participants with normal or correctedtonormal vision were recruited to participate in six experiments (86 females, 10 lefthanded, mean age ± SD: 25.00 ± 4.32; Exp1: n = 20; Exp2: n = 20; Exp3: n = 20; Exp4: n = 23; Exp5: n = 24; Exp6: n = 21). Participants were reimbursed for their time and could earn an additional performancebased bonus (see below). The experiments were conducted in accordance with local ethical guidelines and all participants provided written informed consent. The study was approved by the University of Oxford Central University Research Ethics Committee.
Experimental paradigm
All six experiments were based on the same psychophysical task. On each trial, participants had to judge whether the average orientation of a circular array of gratings (Gabor patches; see Fig. 1) was tilted clockwise (CW) or counterclockwise (CCW) relative to horizontal. The average orientation of the gratings in each trial was randomly selected from a mixture of two Gaussian distributions (centred at 3° either side of the horizontal axis, respectively, and with 8° of standard deviation). We manipulated encoding noise and integration noise by varying two features of the array in a factorial way manner: the root mean square contrast (rmc) of the individual gratings, which affects the difficulty of encoding the stimulus array, and the variability of the orientations of the individual gratings (std), which affects the difficulty of integrating orientations across the stimulus array. The number of contrast and variability conditions varied between experiments: in Experiments 1–3, three contrast levels (rmc = {0, 0.16, 0.6}) and three variability levels (std = {0°, 4°, 10°}); in Experiments 4–6, two contrast levels (rmc = {0.15, 0.6}) and two variability levels (std = {0°, 10°}). The stimulus array was presented for 150 ms and was followed by a 3000 ms choice period. Participants indicated their choice by pressing the right (CW) or the left (CCW) arrowkey on a QWERTY keyboard. They received feedback about choice accuracy, before continuing to the next trial. If no response was registered within the choice period, the word “LATE” appeared at the centre of the screen, and the next trial was started. Experiments 1–3 consisted of 1296 trials, divided into 36 blocks of 36 trials each. Experiments 4–6 consisted of 1200 trials, divided into 32 blocks of 40 trials each.
In Experiments 1 and 2, participants were presented with a cue to the prior probability of each stimulus category. The cue was presented 700 ms before the onset of the stimulus array and remained on the screen until a response was registered. An “N” indicated that the two stimulus categories were equally likely, an “R” indicated a 75% probability of a CW stimulus and an “L” indicated a 75% probability of a CCW stimulus. Half of the blocks contained neutral trials (“N”) and the other half contained biased trials (“R” or “L”). The blocks were randomised across an experiment. In Experiment 2, after having made a choice, participants were required to indicate the probability that the choice is correct by moving a sliding marker along a scale (50–100% in increments of 1%). In Experiment 3, on half of the blocks, participants could opt out of making a choice and receive the same reward as for a correct choice with a 75% probability. There was no prior cue. In Experiment 4, after having made a choice, participants had to categorize (high vs. low) either the contrast or the variability of the stimulus array. Participants received trialbytrial feedback about the categorisation judgement. The judgement types were counterbalanced across trials. In Experiment 5, for each block of trials, we fixed the contrast or the variability level while varying the other feature. In Experiment 6, on half of the blocks, the stimulus array consisted of eight gratings and, on the other half of blocks, the stimulus array consisted of four gratings. Further experimental details are provided in the Supplementary Methods.
Statistical analyses
All statistics are reported at the group level. We performed twoway analyses of variance (reported throughout the text as ANOVAs) with participants as a random variable to test the effects of contrast and variability on choice accuracy, RTs, cue usage, confidence (Exp2) and optin behaviour (Exp3). We performed most analyses of choice accuracy and confidence using neutral trials; analyses of cue usage were naturally based on biased trials. We used multiple linear regression and multiple logistic regression to isolate the effect of variability on confidence and optin responses, respectively. Onesample twotailed ttests (reported throughout the text as ttests) were applied to estimate (i) the significance of the difference between behavioural measures across conditions being different from zero, and (ii) the significance of the mean distribution of regression coefficients being different from zero. For the analyses in Fig. 5a, seven participants were excluded because of excessive optout responses, but result were comparable when including them. All pvalues lower than 0.001 are reported as “p < 0.001”, pvalues ≥0.001 but lower than 0.01 are reported as “p < 0.01”, pvalues ≥0.01 but lower than 0.05 are reported as “p < 0.05”. All pvalues ≥0.05 are reported as higher than the closest lower decimal (e.g., a pvalue of 0.175 would be reported as “p > 0.1”), with exception of pvalues between 0.05 and 0.1 which are reported as “p > 0.05”. The degrees of freedom for the ANOVAs are specified using noninteger values when a Greenhouse–Geisser correction has been used to correct for violations of the sphericity assumption.
Computational modelling
We first describe the omniscient model, which takes into account encoding and integration noise and can identify which condition a trial is drawn from (i.e. assigns a probability of 1 to the current condition on a given trial). We then describe the variabilitymixer model, which takes into account integration noise but cannot distinguish the variability conditions (i.e. assigns equal probability to all variability conditions on a given trial), and the noiseblind model, which entirely neglects integration noise. For completeness, we ran six additional models which varied an agent’s awareness of encoding noise and/or ability to discriminate contrast conditions. We only discuss these models in Supplementary Table 1 as they had no support in the empirical data.
We modelled—regardless of the model—an agent’s noisy estimate, x, of the true average orientation, μ, as a random sample from a Gaussian distribution with mean μ and variance σ^{2}:
where σ is the agent’s total level of noise (encoding plus integration noise) in an experimental condition (see below for noise estimation).
We assumed that an omniscient agent’s internal model has, for each condition, a unique pair of categoryconditioned probability density functions (PDFs) over sensory evidence which reflect the total level of noise and the true probability distribution over average orientations (see Fig. 4c for an example). As such, an omniscient agent would have six pairs of PDFs in Experiments 1–3 and four pairs of PDFs in Experiments 4–6. An omniscient agent uses the relevant pair of PDFs to compute the probability of the sensory evidence given a CW and a CCW category:
where cat is the category and cond is the condition. We constructed the PDFs by convolving the true probability distribution over average orientations with a zerocentred Gaussian distribution with variance σ^{2} depending on a participant’s total noise in a condition. Note that the construction of these PDFs is specific to the model in question (see construction of nonomniscient PDFs below) and is the only source of variation in model predictions about choice and confidence.
We assumed that an agent—regardless of the model—would compute the probability of each category using Bayes’ theorem:
where \(p\left( {x{\mathrm{cat}},{\mathrm{cond}}} \right)\) is computed using the relevant PDFs and p(cat) is the prior probability of the category in question as indicated by the prior cue. If the category in question is CW, then the alternative category, cat_{alt} is CCW, and vice versa. On neutral trials, the prior probability of each category is 50%. On biased trials, the prior probability of one category is 75% and the prior probability of the other category is 25%. The computation detailed in Eq. (3) can be thought of as scaling the relevant PDFs by the prior probability of the respective category (see Fig. 4d for an example).
Finally, we assumed that an agent—regardless of the model—makes a decision, d, by selecting the category with higher posterior support and computes confidence in this decision as:
which in our task is directly given by the posterior probability of the chosen category.
Because the omniscient model takes into account encoding and integration noise and knows which experimental condition a trial is drawn from, an agent will (i) be appropriately influenced by the prior cue, (ii) accurately estimate the probability of having made a correct choice, and (iii) opt out of trials when being less than 75% likely to be correct. We now describe the two models which relaxed the omniscient assumptions.
We first consider the variabilitymixer model which takes into account integration noise but cannot distinguish the different variability conditions. Therefore, when estimating the probability of the sensory evidence given a CW and a CCW category, the variabilitymixer marginalizes its estimate over all possible variability conditions (equivalent to an omniscient agent whose PDFs have been mixed across variability conditions). As a result, when orientation variability is low, the PDFs are more overlapping than for the omniscient model. Conversely, when orientation variability is high, the PDFs are less overlapping than for the omniscient model. For these reasons, a variabilitymixer model would display a mixture of under and overconfidence.
Finally, we consider the noiseblind model which neglects integration noise. Like in the case of the variabilitymixer model, a noiseblind agent only has a pair of PDFs for each contrast level but, unlike in the case of a variabilitymixer model, these PDFs only take into account encoding noise. As a result, when orientation variability is nonzero, the PDFs are less overlapping than under either of the two other models (Fig. 4e). A noiseblind agent would therefore tend to hold stronger posterior beliefs (i.e. steeper curves for Fig. 4f). Such stronger posterior beliefs will lead a noiseblind agent to (i) be less influenced by the prior cue than needed, (ii) overestimate the probability of having made a correct choice, and (iii) not opt out of trials when being less than 75% likely to be correct.
We note that these models (as well as the six additional models described in Supplementary Table 1) make the same predictions about choice on neutral trials but differ with respect to (i) choices on biased trials and (ii) confidence and optin behaviour on both neutral and biased trials. Choice probabilities were computed by marginalizing over the distribution of noisy sensory samples on a given trial; note that, for a given sensory sample, the stimulus category with the higher posterior probability is always chosen.
In the aforementioned models, we assumed that an observer’s inferences are conditional on the average orientation of a stimulus array. We made this simplifying assumption because, by design, the average orientation is independent of variability in the orientation of individual items across experimental conditions. However, it is possible that, if we modelled an observer’s inferences as conditional on the orientation of individual items, then integration noise may not be needed to account for the performance cost associated with highvariability stimuli. We simulated performance under this ensemble model, and show that it cannot predict the performance cost associated with highvariability stimuli (Supplementary Note 2 and Supplementary Fig. 2).
Noise estimation
We assumed that each experimental condition was affected by Gaussian noise with a specific standard deviation, σ_{cond}. We assumed that encoding noise depends upon the contrast of the array and that integration noise is proportional to the variability of orientations in the array. We estimated the total level of noise for each condition using four free parameters (three for Experiments 4–6). Two parameters characterised the level of encoding noise for each contrast level: one for low contrast (nC_{low}) and one for high contrast (nC_{high}). The other two parameters (one for Experiments 4–6) characterised the level of integration noise for each variability level: one for medium variability (nV_{med}, only for Experiments 1–3) and one for high variability (nV_{high}). For a given condition, the total level of noise (the standard deviation of the Gaussian noise distribution), σ_{cond}, is thus given by:
where \(\varepsilon \sigma _{{\mathrm{cond}}}\) and \(\iota \sigma _{{\mathrm{cond}}}\) specify the contribution of encoding noise and integration noise, respectively. For instance, for the lowcontrast, highvariability condition, the total level of noise would be given by substituting nC_{low} for \(\varepsilon \sigma _{{\mathrm{cond}}}\) and nV_{high} for \(i\sigma _{{\mathrm{cond}}}\).
We fitted the four noise estimators for each participant by maximizing the likelihood of the participant’s choice using neutral trials only (we used a genetic algorithm with a population size of 100 individuals and a maximum generation time of 1000 generations). We note that, because of our factorial design, we could separate the two sources of noise. We used the fitted parameters for each participant to construct the model PDFs described above. We note that the model predictions pertain to independent features of the data: (i) confidence on neutral trial choices, (ii) choices (and choice probabilities) on biased trials, and (iii) probability of opting out.
The mean ± SEM of the bestfitting values for the four noise parameters (nC_{low}, nC_{high}, nV_{med} and nV_{high}) in units of degrees were: 10.10 ± 1.51, 3.31 ± 0.39, 3.0 ± 0.78 and 6.8 ± 1.0, respectively. Following Eq. (5), the estimated total amounts of noise fitted for the three key conditions (baseline, lowc and highv) were therefore: 3.31 ± 0.39, 10.1 ± 1.51 and 8.0 ± 1.0, respectively. There was a significant difference between the values for the baseline condition and those for the other two conditions (both pvalues < 0.001), but no significant difference between the lowc and highv conditions (pvalue > 0.16).
Psychometric fits
We fitted psychometric curves to the average proportion of clockwise choices using a fourparameter logistic function:
where P is the proportion of CW choices, A_{1} is the right asymptote, A_{2} is the left asymptote, x_{0} is the inflection point and 1/dx is the steepness, and x is the average stimulus orientation at which the proportion of CW choices is evaluated. We computed the proportion of clockwise choices within six bins (quantiles) over average orientations relative to horizontal. The psychometric curves shown in Fig. 2b are for illustration only.
Bias index
We used signal detection theory^{28,29} to calculate the decision criteria, c, separately for trials on which the prior cue favoured CW and trials on which the prior favoured CCW. The decision criterion provides a signed estimate of the degree to which the prior cue biases a participants’ choices independently of their sensitivity to average orientation. We computed the criterion as, \(c =  0.5[{\it{\Phi }}^{  1}({\mathrm{HR}}) + {\it{\Phi }}^{  1}({\mathrm{FAR}})]\), where \({\it{\Phi }}^{  1}\) represents the inverse of the normal cumulative density function, and HR and FAR represent the hit rate (i.e. the proportion of CW trials where participants responded CW) and false alarm rate (i.e. the proportion of CCW trials where participants responded CW), respectively. We then used the difference between c when cued CW (c_{CW}) and c when cued CCW (c_{CCW}) as our measure of cue usage: bias index = c_{CW}−c_{CCW}. Higher values indicate greater cue usage. We computed a bias index for each participant and each experimental condition.
Reporting summary
Further information on experimental design is available in the Nature Research Reporting Summary linked to this article.
Data availability
Anonymised behavioural data and code supporting our main analyses are available via the Open Science Framework (https://doi.org/10.17605/OSF.IO/QYNJG).
References
Ernst, M. O. & Banks, M. S. Humans integrate visual and haptic information in a statistically optimal fashion. Nature 415, 429–433 (2002).
Knill, D. C., Kersten, D. & Yuille, A. in Percept ion as Bayesian Inference (eds. Knill, D. C. & Richards, W.) 1–21 (Cambridge University Press, New York, 1996).
Körding, K. P. & Wolpert, D. M. Bayesian decision theory in sensorimotor control. Trends Cogn. Sci. 10, 319–326 (2006).
Ma, W. J., Beck, J. M., Latham, P. E. & Pouget, A. Bayesian inference with probabilistic population codes. Nat. Neurosci. 9, 1432–1438 (2006).
Mamassian, P., Landy, M. S. & Maloney, L. T. in Probabilistic Models of the Brain Perception and Neural Function (eds. Rao, R., Lewicki, M. & Olshausen, B.) 13–36 (MIT Press, Cambridge, MA, 2002).
Trommershäuser, J., Maloney, L. T. & Landy, M. S. Decision making, movement planning and statistical decision theory. Trends Cogn. Sci. 12, 291–297 (2008).
Kersten, D., Mamassian, P. & Yuille, A. Object perception as Bayesian inference. Annu. Rev. Psychol. 55, 271–304 (2004).
Körding, K. P. & Wolpert, D. M. Bayesian integration in sensorimotor learning. Nature 427, 244–247 (2004).
O’Reilly, J. X., Jbabdi, S., Rushworth, M. F. & Behrens, T. E. Brain systems for probabilistic and dynamic prediction: computational specificity and integration. PLoS Biol. 11, e1001662 (2013).
Sun, J. & Perona, P. Where is the sun? Nat. Neurosci. 1, 183–184 (1998).
Vilares, I., Howard, J. D., Fernandes, H. L., Gottfried, J. A. & Kording, K. P. Differential representations of prior and likelihood uncertainty in the human brain. Curr. Biol. 22, 1641–1648 (2012).
Tversky, A. & Kahneman, D. Judgment under uncertainty: heuristics and biases. Science 185, 1124–1131 (1974).
Hertwig, R. & Erev, I. The description–experience gap in risky choice. Trends Cogn. Sci. 13, 517–523 (2009).
Levitt, S. D. & List, J. A. What do laboratory experiments measuring social preferences reveal about the real world? J. Econ. Perspect. 21, 153–174 (2007).
Jarvstad, A., Hahn, U., Rushton, S. K. & Warren, P. A. Perceptuomotor, cognitive, and descriptionbased decisionmaking seem equally good. Proc. Natl. Acad. Sci. 110, 16271–16276 (2013).
Ackermann, J. F. & Landy, M. S. Suboptimal decision criteria are predicted by subjectively weighted probabilities and rewards. Atten. Percept. Psychophys. 77, 638–658 (2014).
Gershman, S. J., Horvitz, E. J. & Tenenbaum, J. B. Computational rationality: a converging paradigm for intelligence in brains, minds, and machines. Science 349, 273–278 (2015).
Kahneman, D. Thinking, Fast and Slow (Macmillan, London, 2011).
Summerfield, C. & Tsetsos, K. Do humans make good decisions? Trends Cogn. Sci. 19, 27–34 (2015).
Faisal, A. A. & Wolpert, D. M. Near optimal combination of sensory and motor uncertainty in time during a naturalistic perceptionaction task. J. Neurophysiol. 101, 1901–1912 (2009).
Hunt, L. T. What are the neural origins of choice variability? Trends Cogn. Sci. 18, 222–224 (2014).
Juslin, P. & Olsson, H. Thurstonian and Brunswikian origins of uncertainty in judgment: a sampling model of confidence in sensory discrimination. Psychol. Rev. 104, 344 (1997).
Ma, W. J. & Jazayeri, M. Neural coding of uncertainty and probability. Annu. Rev. Neurosci. 37, 205–220 (2014).
Roitman, J. D. & Shadlen, M. N. Response of neurons in the lateral intraparietal area during a combined visual discrimination reaction time task. J. Neurosci. 22, 9475–9489 (2002).
Botvinick, M. M., Braver, T. S., Barch, D. M., Carter, C. S. & Cohen, J. D. Conflict monitoring and cognitive control. Psychol. Rev. 108, 624 (2001).
Eriksen, B. A. & Eriksen, C. W. Effects of noise letters upon the identification of a target letter in a nonsearch task. Percept. Psychophys. 16, 143–149 (1974).
MacLeod, C. M. Half a century of research on the Stroop effect: an integrative review. Psychol. Bull. 109, 163 (1991).
Macmillan, N. A. & Creelman, C. D. Detection Theory: A User’s Guide (Psychology Press, New York, 2004).
Stanislaw, H. & Todorov, N. Calculation of signal detection theory measures. Behav. Res. Methods Instrum. Comput. 31, 137–149 (1999).
Sonnemans, J. & Offerman, T. Is the Quadratic Scoring Rule really incentive compatible? University of Amsterdam. http://faculty.cbpp.uaa.alaska.edu/jalevy/protected/SonnemansOffermanScoringRules.pdf (2001).
Zakay, D. & Tuvia, R. Choice latency times as determinants of postdecisional confidence. Acta Psychol. (Amst.) 98, 103–115 (1998).
Yeung, N. & Summerfield, C. Metacognition in human decisionmaking: confidence and error monitoring. Philos. Trans. R. Soc. B 367, 1310–1321 (2012).
Aitchison, L., Bang, D., Bahrami, B. & Latham, P. E. Doubly Bayesian analysis of confidence in perceptual decisionmaking. PLoS Comput. Biol. 11, e1004519 (2015).
Bang, D. et al. Confidence matching in group decisionmaking. Nat. Hum. Behav. 1, s41562017 (2017).
Hampton, R. R. Rhesus monkeys know when they remember. Proc. Natl Acad. Sci. 98, 5359–5362 (2001).
Kepecs, A. & Mainen, Z. F. A computational framework for the study of confidence in humans and animals. Philos. Trans. R. Soc. Lond. B Biol. Sci. 367, 1322–1337 (2012).
Kiani, R. & Shadlen, M. N. Representation of confidence associated with a decision by neurons in the parietal cortex. Science 324, 759–764 (2009).
Kass, R. E. & Raftery, A. E. Bayes factors. J. Am. Stat. Assoc. 90, 773–795 (1995).
Zylberberg, A., Fetsch, C. R. & Shadlen, M. N. The influence of evidence volatility on choice, reaction time and confidence in a perceptual decision. eLife 5, e17688 (2016).
Wiecki, T. V., Sofer, I. & Frank, M. J. HDDM: Hierarchical Bayesian estimation of the driftdiffusion model in Python. Front. Neuroinformatics 7, 14 (2013).
Beck, J. M., Ma, W. J., Pitkow, X., Latham, P. E. & Pouget, A. Not noisy, just wrong: the role of suboptimal inference in behavioral variability. Neuron 74, 30–39 (2012).
Thurstone, L. L. A law of comparative judgment. Psychol. Rev. 34, 273 (1927).
Brunswik, E. Perception and the Representative Design of Experiments (University of California Press, Berkeley, CA, 1956).
Wyart, V. & Koechlin, E. Choice variability and suboptimality in uncertain environments. Curr. Opin. Behav. Sci. 11, 109–115 (2016).
Bays, P. M. & Husain, M. Dynamic shifts of limited working memory resources in human vision. Science 321, 851–854 (2008).
Cheadle, S. et al. Adaptive gain control during human perceptual choice. Neuron 81, 1429–1441 (2014).
Bach, D. R. & Dolan, R. J. Knowing how much you don’t know: a neural organization of uncertainty estimates. Nat. Rev. Neurosci. 13, 572 (2012).
PayzanLeNestour, E. & Bossaerts, P. Risk, unexpected uncertainty, and estimation uncertainty: Bayesian learning in unstable settings. PLoS Comput. Biol. 7, e1001048 (2011).
Bogacz, R., Brown, E., Moehlis, J., Holmes, P. & Cohen, J. D. The physics of optimal decision making: a formal analysis of models of performance in twoalternative forcedchoice tasks. Psychol. Rev. 113, 700 (2006).
Gold, J. I. & Shadlen, M. N. Neural computations that underlie decisions about sensory stimuli. Trends Cogn. Sci. 5, 10–16 (2001).
Drugowitsch, J., Wyart, V., Devauchelle, A.D. & Koechlin, E. Computational precision of mental inference as critical source of human choice suboptimality. Neuron 92, 1398–1411 (2016).
Michael, E., de Gardelle, V., NevadoHolgado, A. & Summerfield, C. Unreliable evidence: 2 sources of uncertainty during perceptual choice. Cereb. Cortex. 25, 937–947 (2013).
Shadlen, M. N. & Kiani, R. Decision making as a window on cognition. Neuron 80, 791–806 (2013).
Simons, D. J. & Levin, D. T. Change blindness. Trends Cogn. Sci. 1, 261–267 (1997).
Acknowledgements
This work was supported by a Wellcome 4yearPhD grant to S.H.C. (0099741/Z/12/Z) and an ERC starter grant to C.S. (281628). The Wellcome Centre for Human Neuroimaging is supported by core funding from Wellcome (203147/Z/16/Z).
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S.H.C., T.E., D.B. and C.S. conceived the study. S.H.C., J.D., D.B. and C.S. designed the experiments. S.H.C. programmed the experiments. S.H.C., J.D. and D.B. performed the experiments. S.H.C. and D.B. analysed the data. S.H.C., D.B. and R.M. developed the models and performed simulations. S.H.C., R.M., D.B. and C.S. interpreted the results. S.H.C. drafted the manuscript. S.H.C., D.B. and C.S. wrote the manuscript. All authors approved the final manuscript.
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Herce Castañón, S., Moran, R., Ding, J. et al. Human noise blindness drives suboptimal cognitive inference. Nat Commun 10, 1719 (2019). https://doi.org/10.1038/s41467019093307
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DOI: https://doi.org/10.1038/s41467019093307
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