Abstract
How consciousness arises from brain activity has been a topic of intense scientific research for decades. But how does one identify the neural basis of something that is intrinsically personal and subjective? A hallmark approach has been to ask observers to judge stimuli as ‘seen’ (conscious) and ‘unseen’ (unconscious) and use post hoc sorting of neural measurements based these judgments. Unfortunately, cognitive and response biases are known to strongly affect how observers place their criterion for judging stimuli as ’seen’ vs. ’unseen’, thereby confounding neural measures of consciousness. Surprisingly however, the effect of conservative and liberal criterion placement on neural measures of unconscious and conscious processing has never been explicitly investigated. Here we use simulations and electrophysiological brain measurements to show that conservative criterion placement has an unintuitive consequence: rather than selectively providing a cautious estimate of conscious processing, it inflates effect sizes in neural measures of both conscious and unconscious processing, while liberal criterion placement does the reverse. After showing this in simulation, we performed decoding analyses on two electroencephalography studies that employ common subjective indicators of conscious awareness, in which we experimentally manipulated the response criterion. The results confirm that the predicted confounding effects of criterion placement on neural measures of unconscious and conscious processing occur in empirical data, while further showing that the most widely used subjective scale, the Perceptual Awareness Scale (PAS), does not guard against criterion confounds. Follow-up simulations explicate how the experimental context determines whether the relative confounding effect of criterion placement is larger in neural measures of either conscious or unconscious processing. We conclude that criterion placement threatens the construct validity of neural measures of conscious and unconscious processing.
Introduction
Psychology has a long history of experimentally investigating the contents of the mind. After Watson rejected introspectionism (Watson, 1914), and the cognitive revolution in turn rejected behaviorism (Baars, 1994), it has become widely accepted that there is middle ground: one can potentially gain access to (some of) the contents of the mind by asking observers to report on these contents. This idea has been the central tenet in what has come to be known as the search for the neural correlate of consciousness (Crick and Koch, 1990; LeDoux et al., 2020). It was realized early on that to determine what consciousness is, one must contrast it with what is not conscious, or else the concept of consciousness is an empty shell (the contrastive approach, see Baars, 1994). This presupposes the idea that one can distinguish between conscious and unconscious processes (so-called dual process models).
Indeed, the idea of a hidden unconscious life that precedes and/or escapes our conscious experience also has a long tradition, starting with the idea of unconscious inference (Helmholtz, 1867), and later in Sigmund Freud’s hidden unconscious (Freud, 1904).
In the 80’s and 90’s of the previous century, this culminated in a heated debate centered around the question of how to experimentally establish whether a stimulus has reached consciousness or not. This debate roughly featured researchers defending the position that one should determine unconscious cognition at an objective detection threshold (Greenwald, 1992; Greenwald et al., 1996, 1989; Snodgrass et al., 2004), whereas others defended the position that only a subjectively defined threshold can establish unconscious cognition (Cheesman and Merikle, 1986; Merikle, 1992), with critical comments on the very notion of dual process models by questioning the existence of unconscious cognition at all (Holender, 1986; Holender and Duscherer, 2004).
The core difference between objective and subjective threshold models is that the subjective threshold approach claims to take consciousness seriously by letting the participants in a study indicate on their own terms whether they experience (see) a stimulus at a certain level of intensity (Baars, 1994). In contrast, the objective threshold approach attempts to establish the stimulus level at which some sensitivity measure is at chance, regardless of their claimed experience (Typically, participants have well above chance objective sensitivity for presentation levels at which they claim that stimuli are ‘subjectively’ invisible (Stein et al., 2021).) and regardless of response criterion or bias (Azzopardi and Evans, 2007; Balsdon and Azzopardi, 2015; Green and Swets, 1966). Once it is established that some stimulus is either subjectively invisible (observer claims not seeing the stimulus) or objectively invisible (observer has zero sensitivity) at a given threshold, the typical recipe for establishing unconscious processing is to show that this stimulus still exerts behavioral effects (e.g. subliminal priming effects on a secondary task) or still undergoes residual neural processing (e.g. as measured through EEG or fMRI) despite being ‘unconscious’.
Objective and subjective measures each have their own problems. Although objective measures seem to align best with a scientific approach to consciousness (replicable, objective, e.g. see Mei et al., 2022; Soto et al., 2019), they do require one to invoke a “Gold Standard of seeing” that in fact does not exist (Koenderink, 2014). Relatedly, they ignore the fact that subjective experience is central to the very definition of consciousness. Indeed, cases have been reported in which subjective experience is reported to be different even when objective performance is equated (Fleming et al., 2010a; Hesselmann et al., 2011; Lau and Passingham, 2006; Persaud et al., 2011).
Furthermore, subjective measures are the measure of choice in paradigms in which physical stimulation is kept identical, which are often introduced to prevent that differences between conscious and unconscious vision can be attributed to physical rather than ‘mental’ differences (so called “threshold” approaches, Sanchez et al., 2020). These arguments question whether objective measures can even capture conscious experience, prompting many to defend subjective measures (Baars, 1994; Dehaene, 2014; Overgaard et al., 2010). Subjective measures on the other hand have been widely criticized for being confounded by effects that are unrelated to conscious experience, such as non-perceptual biases as well as regression to the mean effects (for critical reviews see: Newell and Shanks, 2014; Schmidt, 2015; Shanks, 2017; Soto et al., 2019). Nevertheless, subjective measures have gained considerable popularity in consciousness research over the past 20 years (Dehaene et al., 2003; King et al., 2016; King and Dehaene, 2014; Lamy et al., 2009; Michel, 2022; Overgaard et al., 2010, 2006; Ramsøy and Overgaard, 2004; Salti et al., 2015; Sandberg et al., 2010; Sergent et al., 2005; Sergent and Dehaene, 2004; Soto et al., 2019, 2011; Vugt et al., 2018).
A dominant approach in the subjective threshold literature is to sort trials based on observer’s responses to calculate the average neural activation for ‘seen’ (conscious) versus ‘unseen’ (unconscious) trials. Sorting of trials based on subjectively ‘seen’ or ‘unseen’ responses is known as post hoc sorting, because experimental conditions are established based on the participant’s responses after the experiment has completed. Some proposed phenomena that originate from this approach are unconscious working memory (King et al., 2016; Soto et al., 2011; Soto and Silvanto, 2014; Trübutschek et al., 2017), unconscious error detection (Charles et al., 2013), and even unconscious arithmetic (Sklar et al., 2012), for critical comments see (Shanks, 2017; Stein et al., 2016).
In this manuscript, we show that subjective measures are intrinsically prone to criterion confounds. Arbitrary criterion placement influences the decision about stimulus absence or presence, even when consciousness of the stimulus itself is not affected. Thus, two stimuli that undergo identical sensory processing and result in the same experience might either be reported as seen or as unseen, depending on whether the observer adopts a liberal versus a conservative criterion for deciding whether the threshold for a ‘stimulus present’ decision) was reached. Although some may think that such criterion shifts must reflect changes in conscious experience, this is typically not the case. For example, it is well known that perceptual decisions may be motivated by non-perceptual information, such as the payoff matrix (the perceived utility of certain responses) or by statistical regularities in the environment, even when subjective experience is not affected (Rungratsameetaweemana et al., 2018; Sánchez-Fuenzalida et al., 2023a; White and Poldrack, 2014).
Indeed, when a large group of consciousness researchers at the Association of Scientific Studies of Consciousness (ASSC) conference was asked about the relationship between payoff-based criterion shifts and conscious perception, roughly two thirds answered that they did not think that such shifts involve changes in conscious perception (Q2 in Francken et al., 2022). The criterion problem has been known at least since the advent of signal detection theory (Azzopardi and Evans, 2007; Green and Swets, 1966) and has long been hypothesized to underly many – if not all - subjective threshold effects (Eriksen, 1960; Goldiamond, 1958; Peters and Lau, 2015; Phillips, 2020, 2016). However, when criterion shifts are combined with post hoc sorting on subjective measures of consciousness, this may lead to further unwanted confounds. Here we investigate the influence of criterion shifts on post hoc sorted neural measures of consciousness.
Results
First, we sought to make explicit how – under the assumption of a signal detection theoretic model – neural measures of information processing are expected to behave when selecting trials based on a behavioral response. Interestingly, this exercise has never been undertaken. In signal detection theory (Green and Swets, 1966), the relationship between the response (behavior) of an observer and the signal that the observer operates on, depends on the criterion that the observer applies to that signal. This is depicted in Figure 1A, where a distribution of internal signals resulting from pure noise (distribution on the left), needs to be distinguished from a distribution that results when a signal is added to that noise (distribution on the right). How well the observer can distinguish signal from noise is determined by the distance between the two distributions (d’, expressed in standard deviations).
To decide whether any given internal signal comes from the noise distribution or from the signal distribution, the observer must arbitrarily place a criterion somewhere (i.e. the threshold for responding in a certain way: red line / conservative in the top panel, blue line / liberal in the bottom panel). Signals strengths to the right of the criterion are then classified as ‘seen’, whereas signal strengths to the left are classified as ‘unseen’ by the observer. The subjective measures approach assumes that there is a 1:1 relationship between conscious perception and this criterion, but this need not be the case. Indeed, when levels of uncertainty are high, an identical internal signal may either result in a ‘seen’ or in an ‘unseen’ response depending on where this criterion was placed. Placement of the criterion can depend on many non-perceptual factors, including the perceived utility of certain stimulus-response combinations (the payoff matrix), statistical regularities in the environment (differences in the ratio of noise and signal presentations) but also on the state of the observer (explorative vs apprehensive) and even on small changes in task instructions.
When computing neural measures contingent on responses that are subject to criterion shifts, such uncontrolled criterion effects leak into neural measures that are based on behavioral response selection. For example, when the response criterion shifts from conservative to liberal, as is shown in the example in Figure 1A, the average signal strength within both the seen and the unseen response category decreases (see leftward diagonal lines from conservative to liberal). As a result, when extracting the signals from either response category, one should hypothetically get a decrease in the average signal strength in both ‘unseen’ and ‘seen’ conditions under a liberal criterion when compared to a criterion that is more conservative.
In Figure 1B we used a simple simulation to uncover the effect of criterion shifts on neural processing measures. In this simulation, we randomly generated normally distributed internal ‘signals’, which one may conceptualize as trials in a neuroimaging experiment in which a stimulus is presented. Next, we either applied a liberal or a conservative criterion to the signal strength histograms (Figure 1B, left panels) and computed the average signal strength of the ‘unseen’ (left of criterion) and ‘seen’ (right of criterion) conditions, separately for liberal and conservative (see Methods for details).
These average signal strengths are the equivalent of what would be termed neural measures of unconscious (‘unseen’) and conscious (‘seen’) processing in an experiment that uses subjective measures to establish experimental conditions. Somewhat counterintuitively, a more conservative criterion does not have different effects on the neural measure of ‘unconscious’ processing and on the neural measure of ‘conscious’ processing. Instead, when the two criteria are positioned symmetrically around the mean of the signal distribution as in the left panels of Figure 1B, a more conservative criterion inflates neural measures of both unconscious and conscious processing when compared to a liberal criterion (see the right panel of Figure 1B). Although this consequence of criterion shifts on effect sizes in neural measures based on post hoc sorted trials is clearly implied by signal detection theory, to our knowledge it has not been highlighted in the consciousness literature.
Next, we wondered to what extent such criterion effects become apparent in neural measures of unconscious and/or conscious processing when this method is applied to empirical data. To investigate this, we analyzed two datasets in which a criterion manipulation was applied to a detection task. In both experiments, participants viewed a continuous rapid serial visual presentation (RSVP) of oriented textures while EEG was collected (see Figure 2A and 2B). The sequence of textures was always identical, except that the fifth texture either contained a texture-defined square of lines orthogonal to the background orientation (target trials) or a homogenous texture without such a square (no-target trials). In Experiment 1, which has previously been published by Kloosterman and colleagues (2020, 2019), the participant’s task was to identify the target by pressing ‘yes’ whenever they observed a square (detection experiment, see Figure 2A). To manipulate their decision criterion, they were either punished using an aversive tone with a small monetary deduction for misses (liberal condition) or an aversive tone with a small monetary deduction for false alarms (conservative condition).
In a second experiment, we had a different group of participants perform the same task, this time responding using the Perceptual Awareness Scale (PAS: Ramsøy and Overgaard, 2004). This scale allows observers to indicate the strength of their experience at a more fine-grained resolution ranging from [0] “No experience” to [3] “A clear experience” (PAS experiment, see figure 2B and Methods for full description of the four response categories). The underlying assumption is that the PAS that selecting [0] will only occur if trials are ‘truly’ unseen, so that unconscious processing is not overestimated, as may happen in dichotomous or other types of scales (Overgaard et al., 2006; Overgaard and Sandberg, 2021; Sandberg et al., 2010). The PAS was developed to be able to resolve the inability to externally calibrate subjective content, and as such its ultimate goal seems to be to be impervious to non-perceptual criterion shifts. However, despite its popularity, the degree to which the PAS is robust to non-perceptual criterion shifts has never been explicitly investigated. Here, to counter criterion shifts when using the PAS, we further explicitly instructed observers to respond in line with their experience: “Even though you receive feedback about the correctness of your responses, it is very important that you keep responding according to what you actually experience, using the Perceptual Awareness Scale. Only press 0 if you are 100% convinced that no square appeared and only press 3 if you are 100% convinced that a square appeared.” The criterion manipulation was applied by counting PAS0 responses on target trials as misses, and PAS1, PAS2, or PAS3 responses on no-target trials as false alarms (as is common practice, e.g. Soto et al., 2011). Aside from response mode and target presentation duration (Experiment 1: 40 ms, Experiment 2: 30 ms), both experiments were virtually identical (see Methods for other minor differences).
Behaviorally, the criterion manipulation (liberal vs conservative) resulted in a strong criterion shift in both experiments, expressed in concomitant increases of both hits (responding “seen” when a target was presented) and false alarms (responding “seen” when no target was presented) for liberal when compared to the conservative condition (see left panels of Figure 2C and 2D). In contrast, sensitivity – simplified here as the hit rate minus the false alarm rate – remained largely unchanged (right panel of Figure 2C and 2D). To quantify the success of the criterion manipulation in Experiment 1, we computed the signal theoretic parameter estimates criterion c (liberal: -0.30, conservative: 0.73) and sensitivity d’ (liberal: 2.12, conservative: 2.39). This confirmed that the criterion manipulation in Experiment 1 was successful, and that it exerted a much larger effect on criterion (hedges g=2.84) than on d’ (hedges g=0.30).
The behavioral data of Experiment 2 were analyzed in the same way as Experiment 1, this time sorting trials using the four PAS levels, conceptualizing the PAS as a type I response scale, with PAS0 indexing absent responses and PAS1-3 indexing present responses. We reasoned that if participants can maintain a stable response criterion reflecting their experience under the PAS, we should not observe criterion shifts. In contrast, however, we observed strong criterion shifts on all levels of the PAS, as can be seen from concomitant increases of both hits and false alarms for liberal when compared to the conservative condition (see left panels of Figure 2D), while sensitivity (collapsing PAS1, PAS2 or PAS3 as ‘seen’ responses) was only slightly higher for conservative compared to liberal (see the right panel of Figure 2D). This shows for the first time, that all levels of the PAS are affected by criterion shifts, questioning the construct validity of the measure (see Discussion).
Computing the corresponding signal theoretic estimates for Experiment 2 confirms this result for criterion c (liberal: -0.59, conservative: 0.60) and sensitivity d’ (liberal: 1.29, conservative: 1.59). Effect sizes on these measures show that the criterion manipulation in Experiment 2 worked and that it exerted a much larger effect on criterion (hedges g=2.02) than on d’ (hedges g=0.42), just as we observed in Experiment 1.
Next, to establish the effect of criterion shifts on neural measures, we turned to classification performance of EEG data as a measure of neural processing (Fahrenfort et al., 2018). First, a linear discriminant analytic (LDA) classifier was trained for each participant using all trials from all sessions (3 sessions in Experiment 1, 2 sessions in Experiment 2) to discriminate target from no-target trials based on EEG data, irrespective of seen/unseen responses and irrespective of the response criterion. To maximize signal-to-noise ratio, we applied a leave-one-person-out cross validated decoding scheme by using all classifiers from all participants except the participants that was being tested (separately for Experiment 1 and for Experiment 2). This leave-one-person-out cross validation procedure maximized the available data for training without requiring k-folding on subsets of cells with low response counts, so that all test sets were classified by the same fully independent classifiers. A single time series of classification performance across time was obtained for every participant (every testing set) by averaging classification performance across all classifiers that tested that set (see Methods and supplementary Figure S2 for details). We maximized signal-to-noise ratio by performing classification using occipitoparietal electrodes, as these are known to be most sensitive to these stimuli (Fahrenfort et al., 2017, 2008, 2007).
Different electrode selections (all electrodes or only occipital electrodes) yielded qualitatively similar results.
In a first step, we computed classifier performance over time across all trials (irrespective of responses or condition) in the experiment, separately for Experiment 1 and Experiment 2. We subsequently computed the average classification performance across both experiments (see Figure 3A, left panel) and identified three times at which local maxima occurred in this average (137 ms, 266 ms and 430 ms). These peaks reflect stages that are often identified in similar experiments that investigate the time course of perceptual organization (Fahrenfort et al., 2017, 2008, 2007). Figure 3A (right panel) shows that these peaks have highly similar topographic maps of current source density, obtained from the forward transformed weights of the training data from the selected peaks for both experiments (Haufe et al., 2014). To keep multiple comparisons to a minimum, further testing was carried out on the time points at which these three peaks occurred. Note that classification performance was higher for Experiment 1 than for Experiment 2, as this experiment had 3 sessions instead of 2, and target stimuli were presented for 40 ms instead of 30 ms (which also resulted in a higher behavioral d’ for Experiment 1 than for Experiment 2). Note that this has no bearing on the relevant hypothesis tests, because hypothesis testing effects are only within, and not between experiments (i.e. the only relevant difference is between conservative and liberal, not between Experiment 1 and Experiment 2).
Next, to investigate the effect of these criterion shifts on neural measures, we determined how classification performance was affected by post hoc sorting trials based on response categories, separately for decisions made under a liberal criterion and under a conservative criterion. We applied a standard post hoc sorting procedure to the EEG data of each experiment, creating a conscious condition of ‘seen’ figure trials and an unconscious condition of ‘unseen’ figure trials, separately under a conservative and a liberal criterion. For Experiment 1, the difference between seen and unseen was operationalized as participants either giving a ‘yes’ response (=’seen’) or no response at all (=’unseen’). For Experiment 2 the difference between seen and unseen was operationalized as giving a response of 1, 2 or 3 on the PAS (=’seen’) or giving a 0-response on the PAS (=’unseen’).
To ensure that differences resulting from post hoc sorting could not be explained by differences in signal-to-noise ratio resulting from disparities in trial counts in the testing set, we equated trial counts between the liberal and conservative condition within each participant by randomly selecting the same number of trials from overrepresented cells (for Experiment 1, this was done at the level of ‘seen’ and ‘unseen’ responses, for experiment 2 the trial counts were equated at each of the PAS levels, see methods for details). As a result, response-contingent conditions in the liberal and conservative conditions had identical input for all classification analyses. Although different trial counts in the testing set might affect the precision with which AUC is estimated in a decoding analysis, it does not affect the size of AUC itself. Trial count equation was merely performed to make sure the liberal and conservative condition were as comparable as possible. Analyzing the data without equating trial counts resulted in qualitatively identical results.
We then extracted classifier performances at the aforementioned peaks under both a conservative and a liberal criterion, separately for the ‘seen’ and ‘unseen’ conditions, and separately for Experiment 1 and Experiment 2. For Experiment 2, we initially collapsed (averaged) the three ‘seen’ PAS levels (1, 2, 3) into a single ‘seen’ level, so that the visibility factor of Experiment 1 and Experiment 2 would have the same two levels. We then entered these in a large 2 (experiment) x 2 (visibility) x 2 (criterion) x 3 (latency) repeated measures ANOVA with experiment as a between group factor. The result of this ANOVA showed strong main effects of experiment (Exp1 vs Exp2: F1,40=38.68, p<10-6, η²p=0.49), visibility (seen vs unseen: F1,40=204.01, p<10-16, η²p=0.84), criterion (liberal vs conservative: F1,40=20.98, p<10-4, η²p=0.34) and latency (137 ms, 266 ms and 430 ms: F1.79,80=33.72, p<10-8, η²p=0.46), see Supplementary Table S1 for the full ANOVA.
First, we asked whether the criterion shift significantly affected classification performance after post hoc sorting, which was confirmed by the highly significant main effect of criterion. This can also be seen in Figure 3B, where we first show the main effect of criterion separately for Experiment 1 (detection) and Experiment 2 (PAS) collapsed across ‘seen’ and ‘unseen’ trials. These data confirm - as was predicted from our simulation – that post hoc sorting results in a large criterion effect, with higher classification performance for the conservative than for the liberal condition. The consistency of the effect is further supported by the fact that criterion did not significantly interact with experiment (F1,40=1.38, p=0.25, η²p=0.03). Criterion did interact with visibility (F1,40=5.36, p=0.026, η²p=0.12), and with latency (F1.75,69.80=4.44, p=0.02, η²p=0.1), indicating that criterion effects on neural measures manifested differentially in different visibility levels and at different moments in time. Indeed, in both experiments the criterion effect occurs at long latencies (266 ms and 430 ms) but not at the short latency of 137 ms, as was established using one-sided t-tests (conservative > liberal) for simple effects in each of the three latencies for each of the two experiments (see Figure 3B, for the complete time courses of these experiments see supplementary Figure S1A). Finally, there was a highly significant 3-way interaction between criterion, experiment, and visibility (F1,40=18.47, p<10-3, η²p=0.32), which we will expound on in much more detail further down below.
An alternative explanation for these findings might be that the criterion effect is not driven by response-contingent post hoc sorting, but rather that the conservative condition just has higher classification accuracy overall (regardless of post hoc sorting). To investigate this possibility, we re-analyzed the same data without post hoc sorting, i.e. by taking all trials in the conservative condition and in the liberal condition without sorting them into ‘seen’ and ‘unseen’. As in the previous analysis (and using the same classifiers), we extracted classification performance at these peaks under a conservative and under a liberal criterion, separately for Experiment 1 and Experiment 2 (see Figure 3C, for the complete time courses see supplementary Figure S1B).
To test for criterion effects in the absence of post hoc sorting, we then entered these data in a 2 (experiment) x 2 (criterion) x 3 (latency) repeated measures ANOVA with experiment as a between group factor (naturally there was no factor visibility because there was no post hoc sorting). As before, the result of this ANOVA showed strong main effects of experiment (Exp1 vs Exp2: F1,40=28.45, p<10-5, η²p=0.42), and latency (137 ms, 266 ms and 430 ms: F1.70,67.95=49.95, p<10-12, η²p=0.56), but this time there was no main effect of criterion (liberal vs conservative: F1,40=1.16, p=0.29, η²p=0.03), see Supplementary Table S2 for the full ANOVA. Figure 3C shows the effect of criterion separately for the two experiments, with one-sided post hoc t-tests (conservative > liberal) for each of the three latencies. This figure shows that – if anything - the criterion effect is in the opposite direction of the effect observed in Figure 3B, further confirming that the criterion effects in Figure 3B are due to post hoc sorting and not due to general effects of decoding sensitivity in the conservative versus the liberal condition.
Having established the specificity of the post hoc sorting effect, we return our attention to the initial post hoc sorting analysis (Figure 3B and Supplementary Table S1). In this analysis, we observed a small 2-way interaction between visibility and criterion as well as a highly significant 3-way interaction between experiment, criterion, and visibility as noted above (F1,40=18.47, p<10-3, η²p=0.32), also see Supplementary Table S1. This would suggest that Experiment 1 and Experiment 2 contain different post hoc sorting criterion effects on the ‘seen’ and the ‘unseen’ condition. To investigate this further, we performed separate ANOVAs for Experiment 1 (Figure 4A) and Experiment 2 (figure 4B).
For Experiment 1, we performed a 2 (visibility) x 2 (criterion) x 3 (latency) repeated measures ANOVA (see Supplementary Table S3 for the full ANOVA). This analysis again shows strong main effects of visibility (F1,15=81.38, p<10-6, η²p=0.84), criterion (F1,15=13.89, p<0.01, η²p=0.48), and latency (F2,30=37.13, p<10-8, η²p=0.71), but more importantly, it also shows that criterion strongly interacts with visibility in Experiment 1 (F1,15=11.06, p<0.01, η²p=0.42). One-sided t-tests for simple effects (conservative > liberal) revealed that the criterion effects were only significant in the ‘unseen’ condition (Figure 4A, left panel), but not in the ‘seen’ condition (Figure 4A, right panel), and - as established before – that these effects only appear in the late 266 ms / 430 ms latencies as opposed to the early 137 ms latency.
To investigate the interaction between visibility and criterion in Experiment 2, we performed the same analysis in a 4 (visibility) x 2 (criterion) x 3 (latency) repeated measures ANOVA, this time maintaining the four PAS responses as separate levels in the factor visibility (see Supplementary Table S4 for the full ANOVA). Again, this analysis confirmed strong main effects of visibility (F2.37,59.22=67.29, p<10-16, η²p=0.73), criterion (F1,25=10.10, p=0.004, η²p=0.29), and latency (F1.89,47.28=13.26, p<10-4, η²p=0.35), as observed in Experiment 1. Moreover, this experiment-specific ANOVA confirms that here too, criterion interacts with visibility (F2.29,41.37=2.86, p=0.06, η²p=0.10). However, the direction of the interaction is very different from Experiment 1. Post hoc t-tests for simple effects (conservative > liberal) revealed that in Experiment 2, the criterion effects were predominantly in the ‘seen’ conditions of the PAS (PAS1, PAS2 and PAS3, see Figure 4B, 2nd, 3rd and 4th panel), but not in the ‘unseen’ condition (PAS0, see Figure 4B, leftmost panel), whereas Experiment 1 showed a significant effect in ‘unseen’ but not in ‘seen’ (and again only at late 266 ms and/or 430 ms latencies). These differential effects of the criterion on ‘seen’ and ‘unseen’ across experiments explains the highly significant three-way interaction between criterion, experiment, and visibility in the initial ANOVA in which Experiment was incorporated as a factor.
Together, these results confirm clear criterion-effects in both Experiment 1 and Experiment 2 due to post hoc sorting, as was predicted from our initial simulations. However, comparing Experiment 1 and Experiment 2 also shows that these criterion effects are most prominent in the ‘unseen’ condition for Experiment 1, while being most prominent for the ‘seen’ conditions (PAS1, PAS2 and PAS3) in Experiment 2. Wondering why this might be, we went back to our simulations to determine what parameters influence whether a criterion shift is expressed more strongly in ‘unseen’ or in ‘seen’ conditions. To determine this, we separately manipulated two main parameters in our model: sensitivity (the distance between the noise and the signal distribution) and overall criterion (whether the conservative and liberal criterion are either on the left or on the right side of the signal distribution).
Figure 4C-F show the result of these simulations. First, we manipulated the degree of sensitivity (Figure 4C-D), while keeping the response thresholds for responding ‘seen’ or ‘unseen’ the same. When sensitivity is low (Figure 4C, left panels), a small criterion shift is more likely to have a large effect on the neural measure in the ‘seen’ condition after post hoc sorting (Figure 4C, right panel). Conversely, when sensitivity is high (Figure 4D, left panels) the same criterion shift is more likely to have a large effect on the ‘unseen’ condition (Figure 4D, right panel). These simulations show that under identical signal detection thresholds, a change in sensitivity (for example when showing higher strength stimuli, or when an observer is more attentive), can have a large differential impact on the neural measures in ‘seen’ and ‘unseen’ conditions, making their interpretation intrinsically problematic.
In a second simulation, we looked at the effect of overall criterion shifts (Figure 4E and 4F), while keeping sensitivity the same. When the overall criterion is conservative (Figure 4E, left panels), a small criterion shift might have a large effect on the neural measure in the ‘seen’ condition after post hoc sorting (Figure 4E, right panel), whereas when the overall criterion is liberal (Figure 4F, left panels) the same criterion shift can have a large effect in the ‘unseen’ condition (Figure 4F, right panel). This shows that small criterion shifts can have a differential impact on the effect size in neural measures of ‘seen’ and ‘unseen’ stimuli, even when sensitivity stays the same, depending on whether the overall criterion is liberal or conservative, again making the interpretation of such effects problematic.
Thus, criterion shifts can differentially confound neural measures of conscious or unconscious processing, depending both on overall criterion and sensitivity. The direction of this influence can be counterintuitive, is difficult to predict, and cannot be controlled experimentally. Interestingly, Experiment 1 has a much higher sensitivity than Experiment 2 (both in terms of classification accuracy and in terms of behavioral sensitivity, as pointed out before). This provides a compelling explanation for our finding that experiment 1 (detection) shows the largest effect of the criterion shift in the unseen condition, whereas for experiment 2 (PAS) the largest effect was observed in the PAS1 condition and up, which is nicely in line with the predictions from our simulation in Figure 4C-D. Importantly, these factors either cannot be controlled in principle (criterion) and/or are not controlled in practice (sensitivity), which questions the construct validity of subjective measures under post hoc sorting. In the discussion, we consider what these results mean for the future of subjective measures in consciousness research.
Discussion
In this manuscript, we have shown through simulation that post hoc sorting on ‘seen’ and ‘unseen’ responses causes neural effect sizes in ‘seen’ and ‘unseen’ conditions to become stronger under a conservative compared to a liberal response criterion. To test this claim empirically, we analyzed data from two experiments in which criterion shifts were induced experimentally (one using a simple detection task, one using the PAS). We found that in both experiments, criterion shifts modulated effect size in neural measures of ‘unconscious’ (unseen) and/or ‘conscious’ (seen) processing. Finally, we showed through simulation that such criterion shifts can either predominantly impact the neural measure of ‘unconscious’ or of ‘conscious’ processing (or both), depending on the sensitivity of observers and how they place their criterion based on the experimental context.
Together, these data show that criterion shifts confound neural measures of conscious and unconscious processing under post hoc sorting. Such confounds potentially contaminate studies of unconscious cognition (King et al., 2016; Soto et al., 2011) as well as studies that apply post hoc sorting to reveal neural measures of consciousness through a contrastive approach (Boxtel et al., 2010; Hesselmann et al., 2011; Hesselmann and Malach, 2011; Levinson et al., 2021; Melloni et al., 2011; Ress and Heeger, 2003; Rolke et al., 2001; Salti et al., 2015; Sanchez et al., 2020; Sergent et al., 2005; Stein et al., 2021; Vugt et al., 2018; Wyart and Tallon-Baudry, 2008). Concretely, the contrast “seen>unseen”, used in neuroimaging studies to isolate the neural basis of consciousness, can either result in strong or in weak differences between conditions, depending on the response criterion that was adopted by the observers.
Unfortunately, arbitrary criterion placement is intrinsic to decision making, and is known to be affected by many factors that are not controlled between, or even within experiments. Context is known to have a large effect on how observers place their criterion. For example, the ratio of targets to non-targets (the base-rate), the strength of the target stimulus compared to noise (the signal-to-noise ratio), the utility of certain stimulus-response combinations (the payoff matrix), and even small changes in task instructions are all known to affect the response criterion (Fleming et al., 2010b; Kloosterman et al., 2019; Rakhshan et al., 2018; Supèr et al., 2001; White and Poldrack, 2014). So even if some criterion shifts may have a perceptual origin (Meyerhoff and Scholl, 2018; Witt et al., 2015), the omnipresence of arbitrary criterion placement due to non-perceptual influences (Sánchez-Fuenzalida et al., 2023b, 2023a) threatens the construct validity of subjective measures in consciousness research.
Relatedly, criterion shifts also threaten the construct validity of the PAS. Experiment 2 shows that all levels of the PAS are sensitive to the criterion manipulation, even when explicitly instructing participants to only respond according to their experience. This finding is in line with evidence showing similar effects on related subjective measures, such as confidence judgements. For example, both payoff and base-rate induced criterion shifts not only result in a bias on first order decisions, but also affect how second order confidence judgements are distributed (Lebreton et al., 2019, 2018; Locke et al., 2020), also see (Peters et al., 2017). Indeed, recent experiments from our lab have confirmed that payoff and base-rate induced criterion shifts affect confidence scores even when perceptual experience is not affected (Sánchez-Fuenzalida et al., 2023b).
Some may argue that the usage of the PAS in a context in which criterion shifts are experimentally induced is not the spirit in which the PAS was devised. One might even claim that experiment 2 does not make use of the PAS because the criterion was explicitly manipulated in this study, and that one should always take care to extensively calibrate the PAS to subjective content in every experimental context (Sandberg and Overgaard, 2015). However, proper instruction does not resolve this issue. Any context – experimentally induced or not - influences the criterion in some way, and if there is no way to enforce that the adopted criterion is an unwavering threshold on subjective experience (and nothing else), any subjective measure is potentially prone to confounds of a non-experiental nature. Without resolving this, any experiment remains open to the critique that the participants in the study may not have adopted the subjective scale as it was intended, for whatever reason.
Indeed, critics of the current experiment would voice exactly this concern: that the participants did not adopt the PAS as it was intended due to wrong instruction and/or due to the experimental context. As such, the current experiment can be viewed as a caricature of actual experimental practice. For example, depending on how ‘calibration to subjective content’ is done and the experimental context that is generated, some may show that blindsight does not exist (Mazzi et al., 2016; Overgaard et al., 2008), while others may use the same subjective scale to show that unconscious working memory does exist (King et al., 2016; Soto et al., 2011). Plausibly, such patterns of results can be reversed when authors would adopt different calibration procedures or invoke different experimental contexts in their experiments, without any objective way of maintaining or quantifying the construct validity of the adopted subjective scale. Importantly, there is no such thing as a criterion-free experimental context. As pointed out in the beginning of this discussion and in our simulations, many dimensions that are not controlled between experiments, will have a large effect on the criterion even without manipulating it explicitly/experimentally.
Thus, researchers studying consciousness are faced with a difficult conundrum. On the one hand, many view subjective measures as a crucial behavioral marker of the presence or absence of consciousness (Baars, 1994; Dehaene, 2014; Overgaard et al., 2010). On the other hand, subjective measures do not reliably measure the construct they intend to measure due to criterion confounds. A potential way out of this conundrum has been a proposal by Peters & Lau (2015). They combined an objective, first order judgment with a criterion-free subjective measure by having participants place bets (as proxy for subjective reports) on their objective judgment. Trials consisted of two intervals, only one of them containing a grating target, and subjects were asked to guess grating orientation for both intervals and place a bet on which of these two judgements is deemed as more likely to be correct. They argued that above-chance objective performance in the absence of subjective insight measured in this criterion-free way would reflect unconscious perception. One may debate however whether this would save the intended nature of subjective measures, as the bet that participants are forced to place on one of the two intervals seems equivalent to an objective two-interval forced choice task. Without making any final judgement on this matter, we point out that saving the construct validity of subjective measures requires one to solve the criterion problem (Morgan et al., 2013). Without a properly experimentally defined procedure for doing so, their construct validity will remain under threat.
Summarizing, aside from the effect of the criterion on behavioral responses themselves, we show both empirically and in simulation that post hoc trial sorting of neural data on subjective measures can have unintuitive consequences depending on the experimental context (i.e. depending on the criterion that participants adopt). Experimental contexts that induce conservative behavioral responses on subjective measures will overestimate estimates neural correlates of both ‘unconscious’ (unseen) and ‘conscious’ (seen) conditions, whereas experimental contexts that induce liberal behavioral responding do the reverse. As such, criterion placement threatens the construct validity of neural measures of consciousness.
Methods
Simulations
For all simulations, we simulated experiments in Matlab by generating 10,000 normally distributed noise and noise+signal trials using different parameters for the distance between the two distributions as the sensitivity of the system and the criterion that was applied under any given simulation (see OSF for all Matlab code and parameter settings). Decoder classification performance was approximated by conceptualizing the difference d between the average signal strength of signal trials and noise trials after post hoc sorting on criterion as a measure of decoder sensitivity under post hoc sorting (ranging from 0 to ∞). This value was converted to AUC classification performance (ranging from 0.5 to 1), using the formula , in which ϕ is the normal cumulative distribution function. The equivalent Matlab code is AUCsorted = normcdf(dsorted/√2), for the relevant conversion formula from d to AUC see (Ruscio, 2008).
Participants and payment
All participants had normal or corrected-to-normal vision and were recruited at the University of Amsterdam (UvA) in partial fulfillment of first year psychology curricular requirements or for monetary reimbursement (€10 per hour). Participants signed a written informed consent form before the start of the experiment. All procedures were approved by the ethics committee of the University of Amsterdam.
Experiment 1. Sixteen participants (eight females, mean age 24.1 years, SD 1.64, all right-handed) completed three experimental EEG sessions on different days, each session lasting ca. 2 hours. At the beginning of the experiment, participants were informed they could earn a total bonus of €30, on top of their regular pay of €10 per hour or course credit. After completing the last session of the experiment, every participant was paid the full bonus as required by the ethical committee.
Experiment 2. Thirty-four participants completed three experimental sessions: one behavioral training session lasting approximately 45 minutes and two experimental EEG session lasting 2.5 hours each. The EEG data from twenty-six participants was analyzed (14 female, mean age 23.1 years, SD 3.19, 22 right-handed). Four participants were excluded from analysis due having extremely low trial counts on one or more cells after post hoc sorting on the four response levels of the PAS (<5 trials). Four participants were excluded due to equipment failure and/or human error during data collection resulting in corrupted data. Participants had the opportunity to earn an extra €5 in each EEG session, based on the variable payoff scheme described below. All participants were naïve to the purpose of the study.
Experimental setup and presentation software
Participants completed the experiment in a low-lit, quiet room. Stimuli were shown on a computer monitor, with a refresh rate of 100Hz. The experiment was created on Presentation® software (Neurobehavioral Systems, Inc., Berkeley, CA, www.neurobs.com). Experiment 1: Participants were seated approximately 70 cm away from the monitor.
Experiment 2: Participants rested their heads on a chin rest 73 cm away from the monitor.
Stimuli and RSVP
Stimuli consisted of a continuous semi-random rapid serial visual presentation (RSVP) of full screen texture patterns (see Figure 2). The texture patterns consisted of line elements approximately 0.07° thick and 0.4° long in visual angle. Each texture in the RSVP was oriented in one of four possible directions: 0° [vertical], 45°, 90° or 135°. After a random inter-trial interval containing randomly ordered textures, a fixed order sequence containing 25 textures began. The fifth stimulus of the sequence either contained a texture-defined figure (target, T) or a homogenous texture (nontarget, NT). The fixed sequence contained the following orientations: 45°, 90°, 0°, 90°, T/NT, 0°, 90°, 0°, 90°, 0°, 45°, 0°, 135°, 90°, 45°, 0°, 135°, 0°, 45°, 90°, 45°, 90°, 135°, 0°, 135°. This fixed sequence ensured that the visual stimulation surrounding the target was always the same across trials. The nontarget was a homogeneous diagonally oriented texture (45° or 135°). The target was the same texture but contained an orientation-defined square in the center, of which the surface elements were orthogonally rotated with respect to the background. Orientation of targets and nontargets was randomly selected, while ensuring that each orientation was used in 50% of trials. The visual angle of the target square was approximately 2.4°. In 75% of trials, a target figure was shown, and in 25% no figure was shown.
Experiment 1. Target stimuli were presented for 40 ms (i.e. stimulation frequency 25 Hz). The intertrial interval (ITI) varied randomly between 300 and 2200 ms. The fixation dot was red throughout the experiment.
Experiment 2. Target stimuli were presented for 30 ms (i.e. stimulation frequency of 33.3 Hz). The ITI varied randomly between 1800 and 2200 ms. The onset of the fixed sequence containing a target or a nontarget was signaled by the central fixation dot turning from grey to black. The fixation dot was black during the fixed sequence. After the fixed sequence, the fixation dot changed to green, which indicated that participants could respond.
Task instructions and payoff induced criterion manipulation
Participants were instructed to detect a target in an RSVP stream by pressing a button, while their criterion was manipulated.
Experiment 1. Participants were instructed to press a button using their right hand whenever they observed a target in the continuous RSVP. Although the onset of a trial within the continuous stream of textures was not explicitly cued, the similar distribution of reaction times in target and nontarget trials suggests that participants used the temporal structure of the task even when no target appeared. See Kloosterman et al. (2019) for details. In alternating nine-minute blocks of trials, we actively biased participants’ perceptual decisions by instructing them either to report as many targets as possible while playing an aversive tone after each miss (no button press after presentation of a target, liberal condition), or by instructing them to only report high-certainty targets while playing an aversive tone after each false alarm (button press even when no target was presented, conservative condition).
Participants were told their bonus would be diminished by €0.03 after a miss and diminished by €0.10 after a false alarm. Participants were free to respond at any time during a block whenever they detected a target. A trial was considered a target present response when a button press occurred before the fixed-order sequence ended (i.e. within 0.84 s after onset of the fifth texture containing the (non)target, see Figure 2). The criterion manipulation switched back and forth after every block, so that each session contained both conservative and liberal criterion blocks.
Experiment 2. Participants were instructed to determine whether they observed a target in the continuous RSVP using the Perceptual Awareness Scale (PAS; Ramsoy & Overgaard, 2004). The PAS is a four-point scale, on which participants rate the strength of their experience of a stimulus from 0 to 3.
The following instructions regarding the PAS were given to participants:
Between blocks, participants were reminded of the description of each response option of the PAS. Participants received additional on-screen feedback if they used one response option for less than 10% of responses in the previous block: “You are not using all the possible responses on the scale. If this reflects your experience, that is absolutely fine. Otherwise, here are the categories again:”, followed by the PAS descriptions. This was to ensure participants were always aware of using the scale in full, rather than settling into a pattern of choosing between two responses, for example. Participants were further explicitly instructed to respond only according to what they experienced, regardless of the feedback they received during the experiment:
“Even though you receive feedback about the correctness of your responses, it is very important that you keep responding according to what you actually experience, using the Perceptual Awareness Scale. Only press 0 if you are 100% convinced that no square appeared and only press 3 if you are 100% convinced that a square appeared.” Participants were instructed to respond when the fixation dot changed from grey to green, which occurred at the end of the fixed RSVP sequence. Responses given while the fixation date was not green were not recorded. Participants responded using the index finger of their preferred hand, by pressing keys labelled ‘0’, ‘1’, ‘2’ or ‘3’, corresponding to the responses possible on the PAS. As soon as a response was given, the fixation dot changed to grey and the button pressed was displayed in the center of the screen for 60ms, on top of a stream of textures with a grey fixation dot, so participants could ensure they had pressed the correct key (or, alternatively, correct their finger position for the following trial). An auditory feedback tone was given for either false alarms (conservative condition, responding ‘1’, ‘2’ or ‘3’ when no target was present) or misses (liberal condition, responding ‘0’ when a target was present). In addition, for every tone, €0.01 was deducted from their €5 reward for that session. The criterion manipulation occurred at a session level, so that one feedback scheme was exclusively executed in on session, and the other in the other session. The order of sessions was counterbalanced across participants. There was no break in the stream of textures throughout a block of 144 trials, unless no response was given within the 5s limit. In this case, participants were shown a screen reading “Please respond every time the fixation dot is green about what you just experienced.”, then given a 5s countdown before the stream of textures resumed. Throughout the block, the same texture was never repeated twice in a row. No performance feedback was provided at the end of a block. Participants were informed of how much of the extra reward they earned in each session at the end of all sessions.
EEG sessions
Experiment 1.
Prior to EEG recording in the first session, participants performed a 10-minute practice run of both conditions, in which visual feedback directly after a miss (liberal condition) or false alarm (conservative) informed participants about their mistake, allowing them to adjust their decision bias accordingly. During EEG recording, participants performed six blocks per session lasting ca. nine minutes each. During a block, participants continuously monitored the screen and were free to respond by button press whenever they thought they saw a target.
Each block contained 240 trials, of which 180 target and 60 nontarget trials. The condition of the first block of a session was counterbalanced across participants. There were short breaks between blocks, in which participants indicated when they were ready to begin the next block.
Experiment 2. Prior to collecting EEG, each subject underwent a practice session. The practice session started with a slower version of the task, so participants could familiarize themselves with the structure of the trials, and clearly identify the target, and in which they were familiarized with the PAS scale. Only participants that were able to perform the task with a reasonable accuracy of 30% (hit rate minus false alarm rate) were invited for the subsequent EEG sessions. EEG was collected in two different experimental sessions. A session contained ten blocks of either the liberal or conservative condition (counter-balanced across participants). Each block contained 144 trials (108 target trials, 36 non-target trials), and lasted approximately 9 minutes.
EEG Recording
Continuous EEG data were recorded at 512HZ using a 64-channel BioSemi Active-Two system (BioSemi, Amsterdam, The Netherlands). Two external electrodes were placed on the earlobes, to be used as a reference. Electrooculargraphy (EOG) was recorded using four electrodes: on the outer side of each eye (horizontal) and above and below the left eye (vertical). Horizontal and vertical EOG electrodes were referenced against each other, to obtain information about horizontal eye movements, and vertical eye movements and blinks, respectively. Triggers were sent at the time of response and target presentation, recording the orientation and type of trial (target or catch).
Experiment 1. EEG was recorded from a 48-electrode EEG cap that was slightly modified to include I1 and I2 next to Iz. Other electrodes were placed according to the 10-20 system. The complete list of electrodes was AF3, AF4, C3, C4, CP1, CP2, CP3, CP4, CP5, CP6, Cz, F3, F4, F7, F8, FC1, FC2, FC5, FC6, Fp1, Fp2, Fz, I1, I2, Iz, O1, O2, Oz, P1, P10, P2, P3, P4, P5, P6, P7, P8, P9, PO3, PO4, PO7, PO8, POz, Pz, T7, T8, TP7, TP8.
Experiment 2. EEG was recorded from a standard 64-electrode EEG cap, according to the 10-20 system. The complete list of electrodes was AF3, AF4, AF7, AF8, AFz, C1, C2, C3, C4, C5, C6, CP1, CP2, CP3, CP4, CP5, CP6, CPz, Cz, F1, F2, F3, F4, F5, F6, F7, F8, FC1, FC2, FC3, FC4, FC5, FC6, FCz, FT7, FT8, Fp1, Fp2, Fpz, Fz, Iz, O1, O2, Oz, P1, P10, P2, P3, P4, P5, P6, P7, P8, P9, PO3, PO4, PO7, PO8, POz, Pz, T7, T8, TP7, TP8.
EEG Pre-processing
The EEG data from Experiment 1 was pre-processed as described in detail in Kloosterman et al. (2019), with the only exception that for these analyses no detrending was applied to the data. The data from Experiment 2 was pre-processed using a very similar pre-processing pipeline, as described next. All pre-processing and subsequent analyses were conducted using EEGLAB (Delorme and Makeig, 2004), FieldTrip (Oostenveld et al., 2011) and/or the ADAM toolbox (Fahrenfort et al., 2018) using MATLAB code. All data were referenced to the average voltage of two electrodes attached to the earlobes. Channel locations were looked up according to the standard 10-5 BESA cap. Data were downsampled to 256Hz to reduce time and space required for further pre-processing and analysis. The continuous EEG data were epoched between 100 ms before target presentation and 750 ms after target presentation. An Independent Component Analysis (ICA) was used on epoched and demeaned data to identify and remove eye-blinks. Finally, the data were transformed to Scalp Current Density (CSD) using spherical splines (Perrin et al., 1989), after which the data were baseline-corrected using the interval (-100, 0) ms prior to decoding. No high-pass or low-pass filtering was applied to the data to preclude temporal displacements (Driel et al., 2021; VanRullen, 2011).
EEG decoding analyses
Trials were balanced such that the number of trials within each stimulus-response combination were always the same between the liberal and the conservative condition. To achieve this, trials were randomly selected from the stimulus-response condition with the overrepresented stimulus class to match the condition with fewer responses in number. This was done to ensure that differences between the liberal and conservative conditions could not arise just because more trials were included in one condition than in the other.
EEG data were analyzed using the ADAM toolbox (Fahrenfort et al., 2018), a MATLAB toolbox for multivariate pattern analysis of EEG data. The train-test procedure used to classify EEG data was a leave-one-person-out cross validated decoding scheme. In this procedure, all sessions from each participant were merged, and electrodes were used as features to train an LDA classifier to discriminate between targets (figures) and no-targets (homogenous textures) for every sample in the epoch (-100, 750) ms.
Next, these classifiers were used to test the data sets from all participants, except the one that the classifier had been trained on. This procedure was repeated until all classifiers had tested all data sets, except data from the same participant. For Experiment 1 (N=16), this resulted in 16*15=240 classifier performance sets, and for Experiment 2 (N=26), this resulted in 26*25=650 classifier performance sets. Classifier performance sets that were tested on the same person were subsequently averaged, returning to 16 classifier performance sets for Experiment 1, and 26 classifier performance sets for Experiment 2, which were used for subsequent group level statistics. A graphical depiction of this leave-one-person-out cross validation procedure is shown in supplementary Figure S2. The procedure ensured that train and test sets were fully independent, while maximizing the available training data to evaluate test data, as well as maximizing the generalizability of the results within the tested population. The accuracy measure to establish classifier performance was Area Under the Curve (AUC). Classifiers were trained and tested using the occipitoparietal electrodes in both datasets: Iz, O1, O2, Oz, P1, P10, P2, P3, P4, P5, P6, P7, P8, P9, PO10, PO3, PO4, PO7, PO8, PO9, POz, Pz. Group level ANOVAs on classifier performance scores were performed in JASP (Team, 2023).
Data and code availability
All data and processing code is available from OSF in a repository with DOI:XXX (will be made available prior to publication).
References
- Evaluation of a “bias-free” measure of awarenessSpatial Vision 20:61–77https://doi.org/10.1163/156856807779369742
- Contrastive Phenomenology: A Thoroughly Empirical Approach to Consciousness In: Guzeldere“] [“Ned Block and Owen Flanagan and Güven, editor. The Nature of Consciousness: Philosophical DebatesPSYCHE: An Interdisciplinary Journal of Research On Consciousness. MIT Press :187–202
- Absolute and relative blindsightConscious Cogn 32:79–91https://doi.org/10.1016/j.concog.2014.09.010
- Opposing effects of attention and consciousness on afterimagesProc National Acad Sci 107:8883–8888https://doi.org/10.1073/pnas.0913292107
- Distinct brain mechanisms for conscious versus subliminal error detectionNeuroImage 73:80–94https://doi.org/10.1016/j.neuroimage.2013.01.054
- Distinguishing conscious from unconscious perceptual processesCan J Psychol 40:343–367https://doi.org/10.1037/h0080103
- Towards a neurobiological theory of consciousnessSeminars in the Neurosciences 2:263–275
- Consciousness and the Brain: Deciphering How the Brain Codes Our ThoughtsPenguin USA: Penguin Putnam Inc
- A neuronal network model linking subjective reports and objective physiological data during conscious perceptionP Natl Acad Sci USA 100:8520–8525
- EEGLAB: an open source toolbox for analysis of single-trial EEG dynamics including independent component analysisJ Neurosci Meth 134:9–21https://doi.org/10.1016/j.jneumeth.2003.10.009
- High-pass filtering artifacts in multivariate classification of neural time series dataJ Neurosci Meth 352https://doi.org/10.1016/j.jneumeth.2021.109080
- Discrimination and learning without awareness: a methodological survey and evaluationPsychol Rev 67:279–300
- From ERPs to MVPA Using the Amsterdam Decoding and Modeling Toolbox (ADAM)Front Neurosci 12https://doi.org/10.3389/fnins.2018.00368
- Perceptual integration without conscious accessProceedings of the National Academy of Sciences 114:3744–3749https://doi.org/10.1073/pnas.1617268114
- The spatiotemporal profile of cortical processing leading up to visual perceptionJ Vision 8:12–12https://doi.org/10.1167/8.1.12
- Masking disrupts reentrant processing in human visual cortexJ Cognitive Neurosci 19:1488–1497https://doi.org/10.1162/jocn.2007.19.9.1488
- Relating Introspective Accuracy to Individual Differences in Brain StructureScience 329:1541–1543https://doi.org/10.1126/science.1191883
- Effects of Category- Specific Costs on Neural Systems for Perceptual Decision-MakingJ Neurophysiol 103:3238–3247https://doi.org/10.1152/jn.01084.2009
- An academic survey on theoretical foundations, common assumptions and the current state of consciousness scienceNeurosci Conscious 2022https://doi.org/10.1093/nc/niac011
- Zur Psychopathologie des AlltagslebensBerlin: S. Karger
- Indicators of perception: I. Subliminal perception, subception, unconscious perception: An analysis in terms of psychophysical indicator methodologyPsychol Bull 55:373–411https://doi.org/10.1037/h0046992
- Signal Detection Theory and PsychophysicsPeninsula Publishing. Peninsula Publishing
- New Look 3: Unconscious cognition reclaimedAm Psychol 47:766–779https://doi.org/10.1037//0003-066x.47.6.766
- Three Cognitive Markers of Unconscious Semantic ActivationScience 273:1699–1702https://doi.org/10.1126/science.273.5282.1699
- Unconscious processing of dichoptically masked wordsMem Cognition 17:35–47https://doi.org/10.3758/bf03199555
- On the interpretation of weight vectors of linear models in multivariate neuroimagingNeuroimage 87:96–110https://doi.org/10.1016/j.neuroimage.2013.10.067
- Handbuch der physiologischen OptikLeipzig: Leopold Voss
- Differential BOLD activity associated with subjective and objective reports during “blindsight” in normal observersJ Neurosci 31:12936–12944https://doi.org/10.1523/jneurosci.1556-11.2011
- The Link between fMRI-BOLD Activation and Perceptual Awareness Is “Stream-Invariant” in the Human Visual SystemCereb Cortex 21:2829–2837https://doi.org/10.1093/cercor/bhr085
- Semantic Activation Without Conscious Identification in Dichotic- Listening, Parafoveal Vision, and Visual Masking - a Survey and AppraisalBehav Brain Sci 9:1–23https://doi.org/10.1017/s0140525x00021269
- Unconscious perception: The need for a paradigm shiftPercept Psychophys 66:872–881https://doi.org/10.3758/bf03194980
- A model of subjective report and objective discrimination as categorical decisions in a vast representational spacePhilos T Roy Soc B 369:20130204–20130204https://doi.org/10.1098/rstb.2013.0204
- Brain Mechanisms Underlying the Brief Maintenance of Seen and Unseen Sensory InformationNeuron 92:1122–1134https://doi.org/10.1016/j.neuron.2016.10.051
- Humans strategically shift decision bias by flexibly adjusting sensory evidence accumulationeLife Sciences 8https://doi.org/10.7554/elife.37321
- Boosts in brain signal variability track liberal shifts in decision biaseLife Sciences 9:1–22https://doi.org/10.7554/elife.54201
- The all seeing eye?Perception 43:1–6https://doi.org/10.1068/p4301ed
- Neural Correlates of Subjective Awareness and Unconscious Processing: An ERP StudyJ Cognitive Neurosci 21:1435–1446https://doi.org/10.1162/jocn.2009.21064
- Relative blindsight in normal observers and the neural correlate of visual consciousnessP Natl Acad Sci USA 103:18763–18768https://doi.org/10.1073/pnas.0607716103
- Contextual influence on confidence judgments in human reinforcement learningPLoS Comp Biol 15https://doi.org/10.1371/journal.pcbi.1006973
- Two sides of the same coin: Monetary incentives concurrently improve and bias confidence judgmentsSci Adv 4https://doi.org/10.1126/sciadv.aaq0668
- A little history goes a long way toward understanding why we study consciousness the way we do todayPNAS 117:6976–6984https://doi.org/10.1073/pnas.1921623117
- Cortical and subcortical signatures of conscious object recognitionNat Commun 12:1–16https://doi.org/10.1038/s41467-021-23266-x
- Priors and payoffs in confidence judgmentsAtten Percept Psychophys 82:3158–3175https://doi.org/10.3758/s13414-020-02018-x
- Blind-Sight vs. Degraded-Sight: Different Measures Tell a Different StoryFront Psychol 7https://doi.org/10.3389/fpsyg.2016.00901
- Informative neural representations of unseen contents during higher-order processing in human brains and deep artificial networksNat Hum Behav 6:720–731https://doi.org/10.1038/s41562-021-01274-7
- Expectations change the signatures and timing of electrophysiological correlates of perceptual awarenessJ Neurosci 31:1386–1396https://doi.org/10.1523/jneurosci.4570-10.2011
- Perception without awareness. Critical issuesAm Psychol 47:792–795
- Auditory-induced bouncing is a perceptual (rather than a cognitive) phenomenon: Evidence from illusory crescentsCognition 170:88–94https://doi.org/10.1016/j.cognition.2017.08.007
- How (not) to underestimate unconscious perceptionMind Lang https://doi.org/10.1111/mila.12406
- Linking hypotheses underlying Class A and Class B methodsVisual Neurosci 30:197–206https://doi.org/10.1017/s095252381300045x
- Unconscious influences on decision making: a critical reviewBehav Brain Sci 37:1–19https://doi.org/10.1017/s0140525x12003214
- FieldTrip: Open source software for advanced analysis of MEG, EEG, and invasive electrophysiological dataComput Intell Neurosci 2011https://doi.org/10.1155/2011/156869
- Seeing without Seeing? Degraded Conscious Vision in a Blindsight PatientPLoS ONE 3https://doi.org/10.1371/journal.pone.0003028
- Is conscious perception gradual or dichotomous? A comparison of report methodologies during a visual taskConscious Cogn 15:700–708https://doi.org/10.1016/j.concog.2006.04.002
- The Perceptual Awareness Scale—recent controversies and debatesNeurosci Conscious 2021https://doi.org/10.1093/nc/niab044
- Optimizing subjective measures of consciousnessConscious Cogn 19:682–684https://doi.org/10.1016/j.concog.2009.12.018
- Spherical splines for scalp potential and current density mappingElectroen Clin Neuro 72:184–187https://doi.org/10.1016/0013-4694(89)90180-6
- Awareness-related activity in prefrontal and parietal cortices in blindsight reflects more than superior visual performanceNeuroimage 58:605–611https://doi.org/10.1016/j.neuroimage.2011.06.081
- Human observers have optimal introspective access to perceptual processes even for visually masked stimulieLife Sciences 4https://doi.org/10.7554/elife.09651
- Perceptual confidence neglects decision-incongruent evidence in the brainNat Hum Behav 1https://doi.org/10.1038/s41562-017-0139
- Blindsight is qualitatively degraded conscious visionPsychol Rev https://doi.org/10.1037/rev0000254
- Consciousness and Criterion: On Block’s Case for Unconscious SeeingPhilosophy and Phenomenological Research 93:419–451https://doi.org/10.1111/phpr.12224
- Influence of Expected Reward on Temporal Order JudgmentJ Cognitive Neurosci 32:674–690https://doi.org/10.1162/jocn_a_01516
- Introspection and subliminal perceptionPhenom Cogn Sci 3:1–23https://doi.org/10.1023/b:phen.0000041900.30172.e8
- Neuronal correlates of perception in early visual cortexNat Neurosci 6:414–420
- Missed prime words within the attentional blink evoke an N400 semantic priming effectPsychophysiology 38:165–174
- Expectations Do Not Alter Early Sensory Processing during Perceptual Decision-MakingJ Neurosci 38:5632–5648https://doi.org/10.1523/jneurosci.3638-17.2018
- A Probability-Based Measure of Effect Size: Robustness to Base Rates and Other FactorsPsychol Methods 13:19–30https://doi.org/10.1037/1082-989x.13.1.19
- Distinct cortical codes and temporal dynamics for conscious and unconscious perceptseLife Sciences 4https://doi.org/10.7554/elife.05652
- Decoding across sensory modalities reveals common supramodal signatures of conscious perceptionPNAS 117:7437–7446https://doi.org/10.1073/pnas.1912584117
- Predictions and rewards affect decision-making but not subjective experienceProc Natl Acad Sci 120https://doi.org/10.1073/pnas.2220749120
- Non- sensory information affects confidence during perceptual decision-makingPsyArxiv https://doi.org/10.31234/osf.io/xa4fj
- Using the perceptual awareness scale (PAS)Behavioral Methods in Consciousness Research :181–196https://doi.org/10.1093/acprof:oso/9780199688890.003.0011
- Measuring consciousness: is one measure better than the other?Consciousness and Cognition 19:1069–1078https://doi.org/10.1016/j.concog.2009.12.013
- Invisible Stimuli, Implicit Thresholds: Why Invisibility Judgments Cannot be Interpreted in IsolationAdv Cogn Psychol 11:31–41https://doi.org/10.5709/acp-0169-3
- Timing of the brain events underlying access to consciousness during the attentional blinkNat Neurosci 8:1391–1400https://doi.org/10.1038/nn1549
- Is consciousness a gradual phenomenon? Evidence for an all-or- none bifurcation during the attentional blinkPsychol Sci 15:720–728https://doi.org/10.1111/j.0956-7976.2004.00748.x
- Regressive research: The pitfalls of post hoc data selection in the study of unconscious mental processesPsychon B Rev 24:752–775https://doi.org/10.3758/s13423-016-1170-y
- Reading and doing arithmetic nonconsciouslyProceedings of the National Academy of Sciences 109:19614–19619https://doi.org/10.1037/0096-3445.124.1.22
- Unconscious perception: A model-based approach to method and evidencePercept Psychophys 66:846–867https://doi.org/10.3758/bf03194978
- Working memory without consciousnessCurr Biol 21:R912–R913
- A Novel Framework for Unconscious ProcessingTrends Cogn Sci https://doi.org/10.1016/j.tics.2019.03.002
- Reappraising the relationship between working memory and conscious awarenessTrends Cogn Sci 18:520–525https://doi.org/10.1016/j.tics.2014.06.005
- The human visual system differentially represents subjectively and objectively invisible stimuliPLoS Biol 19https://doi.org/10.1371/journal.pbio.3001241
- Can working memory be non-conscious?Neurosci Conscious 2016https://doi.org/10.1093/nc/niv011
- Two distinct modes of sensory processing observed in monkey primary visual cortex (V1)Nat Neurosci 4:304–310https://doi.org/10.1038/85170
- JASP
- A theory of working memory without consciousness or sustained activityeLife 6https://doi.org/10.7554/elife.23871
- Four common conceptual fallacies in mapping the time course of recognitionFront Psychology 2https://doi.org/10.3389/fpsyg.2011.00365
- The threshold for conscious report: Signal loss and response bias in visual and frontal cortexScience 23https://doi.org/10.1126/science.aar7186
- Behavior: An introduction to comparative psychologyHenry Holt and Co. https://doi.org/10.1037/10868-000
- Decomposing Bias in Different Types of Simple DecisionsJ Exp Psychol Learn 40:385–398https://doi.org/10.1037/a0034851
- Signal Detection Measures Cannot Distinguish Perceptual Biases from Response BiasesPerception 44:289–300https://doi.org/10.1068/p7908
- Neural dissociation between visual awareness and spatial attentionJ Neurosci 28:2667–2679
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