Masking Stimulus Research Articles

Binary vs. continuous experimental designs for the study of unconscious perceptual processing.

Binary vs. continuous conceptualizations of consciousness may have an unstated influence on experimental designs in unconscious perception research. The binary approach aims to compare a conscious condition (e.g., supraliminal, no or weak stimulus masking) to an unconscious condition (e.g., subliminal, heavy stimulus masking). In contrast, continuous designs tend to vary stimulus energy along a near-threshold continuum to determine changes in perception as a function of stimulus energy (or duration). The present study compared two experimental designs, binary vs. continuous, for the influence of target-masked prime stimuli on a Stroop task. The display parameters were inspired by emotional Stroop studies reporting unconscious perception. Neither experiment produced strong evidence of unconscious perception, but the experiment with a continuous design was more informative. We thus recommend sampling a range of near-threshold display parameters to yield straight-forward, unambiguous interpretations.

On the time it takes to judge grammaticality.

The presentation duration of five-word sequences was varied and participants were asked to judge their grammaticality. The five-word sequences were presented for a variable duration randomly selected between 50 and 500 ms with 50-ms steps and were immediately followed by a masking stimulus. Half of the sequences were correct sentences which were randomly intermixed with ungrammatical sequences formed of the same words in scrambled order. We measured the proportion of correct responses for each presentation duration in the grammatical and ungrammatical conditions, and calculated sensitivity and bias from these measures. Both the sensitivity measure (d') and the probability correct responses to grammatical and ungrammatical sequences increased as the stimulus duration increased, with a d' of 2 and an average percent correct close to 87% for the grammatical sequences already attained at 300 ms. The rate of increase in performance diminished beyond 300 ms. Grammatical decision times were faster and more accurate for the grammatically correct sequences, thus indicating that participants were not responding by detecting illegal word combinations in the ungrammatical sequences. On the basis of these findings, we provide an upper estimate of 300 ms as the time it takes to access reliable syntactic information from five-word sequences in French, and we discuss the implications of this constraint for models of reading.

Concurrent Electrodermal and Eyeblink Conditioning With Masked and Unmasked Stimuli

Abstract. The aim of this study was to determine if contingency awareness between the conditioned (CS) and unconditioned stimulus (US) is necessary for concurrent electrodermal and eyeblink conditioning to masked stimuli. An angry woman’s face (CS+) and a fearful face (CS−) were presented for 23 milliseconds (ms) and followed by a neutral face as a mask. A 98 dB noise burst (US) was administered 477 ms after CS+ offset to elicit both electrodermal and eyeblink responses. For the unmasking conditioning a 176 ms blank screen was inserted between the CS and the mask. Contingency awareness was assessed using trial-by-trial ratings of US-expectancy in a post-conditioning phase. The results showed acquisition of differential electrodermal and eyeblink conditioning in aware, but not in unaware participants. Acquisition of differential eyeblink conditioning required more trials than electrodermal conditioning. These results provided strong evidence of the causal role of contingency awareness on differential eyeblink and electrodermal conditioning.

Masking the Detection of Taste Stimuli in Rats: NaCl and Sucrose.

While psychophysical and neurophysiological assessments of taste sensitivity to single chemical compounds have revealed some fundamental properties of gustatory processing, taste stimuli are rarely ingested in isolation. Arguably, the gustatory system was adapted to identify and report the presence of numerous chemicals ingested concurrently. To begin systematically exploring the detectability of a target stimulus in a background in rodents, we used a gustometer to train rats in a 2-response operant task to detect either NaCl (n = 8) or sucrose (n = 8) dissolved in water, and then tested the sensitivity of rats to the trained NaCl stimulus dissolved in a sucrose masker (0.3, 0.6, or 1.0 M, tested consecutively) versus sucrose, or the trained sucrose stimulus dissolved in a NaCl masker (0.04, 0.2, or 0.4 M) versus NaCl. Detection thresholds (EC50 values) were determined for the target stimulus dissolved in each concentration of the masker. Except for 0.04 M NaCl, all masker concentrations tested increased the target stimulus EC50. Target stimulus detectability decreased systematically as masker concentrations increased. The shift in liminal sensitivity for either target was similar when the threshold for the masker was considered. At least for these prototypical stimuli, it appears that the attenuating impact of a masker on the detection of a target stimulus depends on sensitivity to the masking stimulus. Further study will be required to generalize these results and extend them to more complex maskers, and to discern neural circuits involved in the detection of specific taste signals in the context of noisy backgrounds.

Impairment of cyclopean surface processing by disparity-defined masking stimuli.

Binocular disparity signals allow for the estimation of three-dimensional shape, even in the absence of monocular depth cues. The perception of such disparity-defined form depends, however, on the linkage of multiple disparity measurements over space. Performance limitations in cyclopean tasks thus inform us about errors arising in disparity measurement and difficulties in the linkage of such measurements. We used a cyclopean orientation discrimination task to examine the perception of disparity-defined form. Participants were presented with random-dot sinusoidal modulations in depth and asked to report whether they were clockwise or counter-clockwise rotated. To assess the effect of different noise structures on measurement and linkage processes, task performance was measured in the presence of binocular, random-dot masks, structured as either antiphase depth sinusoids, or as random distributions of dots in depth. For a fixed number of surface dots, the ratio of mask-to-surface dots was varied to obtain thresholds for orientation discrimination. Antiphase masks were found to be more effective than random depth masks, requiring a lower mask-to-surface dot ratio to inhibit performance. For antiphase masks, performance improved with decreased cyclopean frequency, increased disparity amplitude, and/or an increase in the total number of stimulus dots. Although a cross-correlation model of disparity measurement could account for antiphase mask performance, random depth masking effects were consistent with limitations in relative disparity processing. This suggests that performance is noise-limited for antiphase masks and complexity-limited for random masks. We propose that use of differing mask types may prove effective in understanding these distinct forms of impairment.

Visual word recognition: Evidence for a serial bottleneck in lexical access

Reading is a demanding task, constrained by inherent processing capacity limits. Do those capacity limits allow for multiple words to be recognized in parallel? In a recent study, we measured semantic categorization accuracy for nouns presented in pairs. The words were replaced by post-masks after an interval that was set to each subject’s threshold, such that with focused attention they could categorize one word with ~80% accuracy. When subjects tried to divide attention between both words, their accuracy was so impaired that it supported a serial processing model: on each trial, subjects could categorize one word but had to guess about the other. In the experiments reported here, we investigated how our previous result generalizes across two tasks that require lexical access but vary in the depth of semantic processing (semantic categorization and lexical decision), and across different masking stimuli, word lengths, lexical frequencies and visual field positions. In all cases, the serial processing model was supported by two effects: (1) a sufficiently large accuracy deficit with divided compared to focused attention; and (2) a trial-by-trial stimulus processing tradeoff, meaning that the response to one word was more likely to be correct if the response to the other was incorrect. However, when the task was to detect colored letters, neither of those effects occurred, even though the post-masks limited accuracy in the same way. Altogether, the results are consistent with the hypothesis that visual processing of words is parallel but lexical access is serial.

A Masked Aversive Odor Cannot Be Discriminated From the Masking Odor but Can Be Identified Through Odor Quality Ratings and Neural Activation Patterns.

Odor masking is a very prominent problem in our daily routines, mainly concerning unpleasant sweat or toilet odors. In the current study we explored the effectiveness of odor masking both on a behavioral and neuronal level. By definition, participants cannot differentiate a fully masked unpleasant odor from the pleasant pure odor used as a masking agent on a behavioral level. We hypothesized, however, that one can still discriminate between a fully masked odor mixture and the pure masking odor on a neuronal level and that, using a reinforcing feedback paradigm, participants could be trained to perceive this difference. A pleasant, lemon-like odor (citral) and a mixture of citral and minor amounts of an unpleasant, goat-like odor (caproic acid) were presented to participants repeatedly using a computer-controlled olfactometer and participants had to decide whether two presented stimuli were the same or different. Accuracy of this task was incentivized with a possible monetary reward. Functional imaging was used throughout the task to investigate central processing of the two stimuli. The participants rated both stimuli as isopleasant and isointense, indicating that the unpleasant odor was fully masked by the pleasant odor. The isolated caproic acid component of the mixture was rated less pleasant than the pleasant odor in a prior experimental session. Although the masked and pure stimuli were not discriminated in the forced-choice task, quality ratings on a dimensional scale differed. Further, we observed an increased activation of the insula and ventral striatum/putamen for the pure in contrast to the fully masked odor, hence revealing a difference in neuronal processing. Our hypothesis that perceptual discrimination and neuronal processing can be enhanced using a reinforcing feedback paradigm is not supported by our data.

Impaired facial emotion perception of briefly presented double masked stimuli in violent offenders with schizophrenia spectrum disorders

Social interactions require decoding of subtle rapidly changing emotional cues in others to facilitate socially appropriate behaviour. It is possible that impairments in the ability to detect and decode these signals may increase the risk for aggression. Therefore, we examined violent offenders with schizophrenia spectrum disorders (SSD) and compared these with healthy controls on a computerized paradigm of briefly presented double masked faces exhibiting 7 basic emotions. Our hypotheses were that impaired semantic understanding of emotion words and low cognitive ability would yield lowest emotion recognition. SSD exhibited lower accuracy of emotion perception than controls (46.1% compared with 64.5%, p = 0.026), even when considering the unbiased hit rate (22.4% compared with 43%, Z = 2.62, p < 0.01). Raw data showed uncommon but significant misclassifications of fear as sad, disgust as sad, sad as happy and angry as surprise. Once guessing and presentation frequencies were considered, only overall accuracy differed between SSD and healthy controls. There were significant correlations between cognitive ability, antipsychotic dose, speed and emotion accuracy in the SSD group. In conclusion, that there were no specific emotion biases in the SSD group compared to healthy controls, but particular individuals may have greater impairments in facial emotion perception, being influenced by intellectual ability, psychomotor speed and medication dosages, rather than specifically emotion word understanding. This implies that both state and trait factors influence emotion perception in the aggressive SSD group and may reveal one source of potential misunderstanding of social situations which may lead to boundary violations and aggression.

Action priming is linked to visual perception in continuous flash suppression.

Visual prime stimuli can affect the processing of following target stimuli even if their visibility is reduced due to visual masking. Prime visibility depends on the stimulus parameters of the prime and those of the mask. Here we explored the effects of prime stimuli and modulated their visibility by continuous flash suppression (CFS). CFS reduces the visibility of a stimulus presented to one eye by simultaneously presenting a series of high-contrast masking stimuli to the other eye. We manipulated the strength of CFS effects on perception and examined how action priming effects of the masked stimuli varied under the same conditions. Prime visibility was modulated by the contrast of the primes (Experiments 1 and 2), the contrast of the masks (Experiments 2 and 3), and by the stimulus onset asynchrony between prime and target stimuli (all experiments). Surprisingly, action priming effects were modulated by these experimental variables in a parallel way. In addition, individual differences between participants in prime visibility correlated with individual differences in action priming. Our findings suggest that action priming and prime perception depend in similar ways on prime contrast, mask contrast, stimulus onset asynchrony, and individual dispositions in CFS. These findings distinguish CFS from other perceptual suppression techniques, such as backward masking, that allow reducing prime visibility without parallel effects on action priming. Our results corroborate the view that CFS interferes with visual processing at early stages in the cortical hierarchy with similar effects on later processing for perception and action.

Objective frequency-specific measurement of hearing threshold using narrow-band chirp stimuli with level-adaptive simultaneous masking

In the past, various simulation and measurement paradigms have been introduced and evaluated in order to improve frequency-specific measurement of the hearing threshold using early auditory evoked potentials (EAEP). Apromising approach for improvement of detection of stimulus response is the usage of frequency-modulated chirp signals, which optimize the temporal synchrony of neuronal responses along aregion of the basilar membrane. This study validated the performance of three generated narrow-band chirp stimuli in combination with alevel-adaptive simultaneous masker on acollective of normally hearing subjects. In this study 25 normal hearing subjects took part after undergoing pure tone audiometry as well as an objective estimation of the auditory threshold using low, middle and high chirp stimuli. The characteristic EAEP parameters were visually identified before statistical analysis. The characteristic latency level function was conducted using measurements within astimulus level range from 80 to 0 dBHL. Afterwards acomparison of objectively verified auditory threshold and subjective auditory threshold was conducted. All objectively determined thresholds of the frequency-specific evoked EAEP were on average below 10 dBHL: low chirp at 8.2 dBHL, middle chirp at 5.8 dBHL and high chirp at 5.4 dBHL. The mean difference compared to subjectively determined auditory thresholds at all frequencies was below 3 dB and was not significant. Brainstem evoked response audiometry (BERA) using aband-limited and level-specific masked chirp stimulus is an efficient method for the determination of frequency-specific excitation thresholds in the clinical routine. The small, insignificant difference compared to the subjectively determined auditory thresholds makes usage of correction factors mostly redundant. Confirming the study results concerning low chirp stimuli so far, the low chirp BERA currently seems to be the method of choice for estimation of auditory threshold at low frequency ranges around 500 Hz.

Masking procedures can influence priming effects besides their effects on conscious perception.

Masked priming has been employed to study the role of consciousness for different levels of visual processing. However, masking procedures differ systematically between studies. To examine these procedural differences we contrasted priming effects with metacontrast masking, which is often applied in the context of perceptual priming, and priming effects with sandwich pattern masking, frequently used in studies on semantic priming. Results indicate that the amount of masking neither affects perceptual nor semantic priming effects in a semantic categorization task when a metacontrast masking paradigm was used. However, perceptual and semantic priming effects increased with increasing prime visibility when a sandwich pattern masking paradigm was used. Findings suggest that different types of masking procedures affect the processing of the masked stimuli in substantially different ways even if the masking effect on conscious perception of these stimuli is comparable.

Visual short-term memory for coherent motion in video game players: evidence from a memory-masking paradigm

In this study, we investigated visual short-term memory for coherent motion in action video game players (AVGPs), non-action video game players (NAVGPs), and non-gamers (control group: CONs). Participants performed a visual memory-masking paradigm previously used with macaque monkeys and humans. In particular, we tested whether video game players form a more robust visual short-term memory trace for coherent moving stimuli during the encoding phase, and whether such memory traces are less affected by an intervening masking stimulus presented 0.2 s after the offset of the to-be-remembered sample. The results showed that task performance of all groups was affected by the masking stimulus, but video game players were affected to a lesser extent than controls. Modelling of performance values and reaction times revealed that video game players have a lower guessing rate than CONs, and higher drift rates than CONs, indicative of more efficient perceptual decisions. These results suggest that video game players exhibit a more robust VSTM trace for moving objects and this trace is less prone to external interference.

Rapid stream stimulation can enhance the stimulus selectivity of early evoked responses to written characters but not faces.

The recognition potential (RP) is an early visually evoked response (~250 ms) whose magnitude is sensitive to object recognizability and related factors. The RP is often measured when objects are embedded in a rapid stream of masking stimuli (the RSS paradigm), especially in reading research. The idea is that RSS provides greater stimulus-dependent variations in RP, compared to the corresponding variations without RSS. However, this idea has never been subject to systematic evaluation. We directly test whether RSS can enhance 2 types of RP stimulus selectivity, by measuring the RP in conditions that only differ in the presence or absence of a masking stream and in the type of stimulus shown. We measure the effect of image inversion on RP for Chinese characters (experiment 1); the effect of orthographical correctness on RP for Chinese characters (experiment 3); and as a control study, the effect of image inversion on the N170 response to faces (experiment 2). To ensure a fair comparison, the earliest negative deflections (RP/N170) measured with and without RSS should at least have similar channel ranges, and topographical distributions of both amplitude and selectivity. Our first set of results clearly supports this. Our main results clearly show an increase in stimulus-selectivity for RSS over non-RSS in both of the RP (Chinese character) experiments, but no such enhancement in the N170 (face) experiment. This provides incentive for investigations into the underlying mechanisms of selectivity enhancement. Our findings may also help to explain contradictory findings between RP/N170 studies that differ only in the use of noise masks, which is sometimes treated as trivial detail in papers that do not reference the RP/RSS literature.

Binding identity and orientation in object recognition.

We tested whether an object's orientation is inherently bound to its identity in a holistic view-based representation at the early stages of visual identification, or whether identity and orientation are represented separately. Observers saw brief and masked stimulus sequences containing two rotated objects. They had to detect if a previously cued object was present in the sequence and report its orientation. In Experiments 1 and 2, the objects were presented sequentially in the same spatial location for 70 ms each, whereas in Experiments 3 and 4 they were presented simultaneously in different spatial locations for 70 ms and 140 ms, respectively. Across all experiments, observers reported the correct orientation for approximately 70% of the positively identified objects, and were at chance in reporting the orientation when they had not recognized the object. This finding suggests that orientation information is accessed after an object has been identified. In addition, when the two objects were presented sequentially in the same spatial location, orientation errors were not random-observers tended to report the orientation of the alternative object in the sequence, indicating misbindings between the identities and orientations of objects that share spatial location. This susceptibility to binding errors was not observed when the objects were in different spatial locations. These results suggest that identity and orientation may be prone to misbinding, and that spatial location may serve to protect their joint integrity.

Human-like perceptual masking is difficult to observe in rats performing an orientation discrimination task.

Visual masking occurs when the perception of a brief target stimulus is affected by a preceding or succeeding mask. The uncoupling of the target and its perception allows an opportunity to investigate the neuronal mechanisms involved in sensory representation and visual perception. To determine whether rats are a suitable model for subsequent studies of the neuronal basis of visual masking, we first demonstrated that decoding of neuronal responses recorded in the primary visual cortex (V1) of anaesthetized rats predicted that orientation discrimination performance should decline when masking stimuli are presented immediately before or after oriented target stimuli. We then trained Long-Evans rats (n = 7) to discriminate between horizontal and vertical target Gabors or gratings. In some trials, a plaid mask was presented at varying stimulus onset asynchronies (SOAs) relative to the target. Spatially, the masks were presented either overlapping or surrounding the target location. In the absence of a mask, all animals could reliably discriminate orientation when stimulus durations were 16 ms or longer. In the presence of a mask, discrimination performance was impaired, but did not systematically vary with SOA as is typical of visual masking. In humans performing a similar task, we found visual masking impaired perception of the target at short SOAs regardless of the spatial or temporal configuration of stimuli. Our findings indicate that visual masking may be difficult to observe in rats as the stimulus parameters necessary to quantify masking will make the task so difficult that it prevents robust measurement of psychophysical performance. Thus, our results suggest that rats may not be an ideal model to investigate the effects of visual masking on perception.

Generalized identity in a successive matching-to-sample procedure in rats: Effects of number of exemplars and a masking stimulus.

Two experiments examined the emergence of generalized identity matching in rats using a successive discrimination procedure with olfactory stimuli. Trials consisted of the presentation of two odors separated by a 1-s interstimulus interval. Responses during the second odor presentation were reinforced only if the two odors were identical. In Experiment 1, rats were trained with two odors and then exposed to sessions that included unreinforced probe trials with novel odors. There was evidence of higher response rates on matching probe trials in some rats, but matching did not approach baseline levels. Additional training with four exemplars produced transfer to novel odors that was equivalent to baseline levels. Experiment 2 tested the possibility that detection of stimulus change, rather than generalized identity, was responsible for the transfer seen in Experiment 1. Thus, a masking odor was inserted during the 1-s interstimulus interval so that stimulus change occurred on all trials. Although response rates on probe trials were lower than baseline rates, above chance transfer to novel stimuli was still observed in four of the five animals tested. These findings support the hypothesis that transfer of matching to novel odors in this successive matching-to-sample paradigm is based on a generalized identity relation.

Neuronal adaptation to sound statistics in the inferior colliculus of behaving macaques does not reduce the effectiveness of the masking noise.

The detectability of target sounds embedded within noisy backgrounds is affected by the regularities that summarize acoustic sceneries. Previous studies suggested that the dynamic range of neurons in the inferior colliculus (IC) of anesthetized guinea pigs shifts toward the mean sound pressure level in irregular acoustic environments. Yet, it is unclear how this neuronal adaptation processes may influence the effectiveness of sounds as a masker, both behaviorally and in terms of neuronal encoding. To answer this question, we measured the neural response of IC neurons while macaque monkeys performed a Go/No-Go tone detection task. Macaques detected a 50-ms tone that was either simultaneously gated with a burst of noise or embedded within a continuous noise background, whose levels were randomly sampled (every 50 ms) from a probability distribution. The mean of the distribution matched the level of the gated burst of noise. Psychometric and IC neurometric thresholds to tones did not differ between the two masking conditions. However, the neuronal firing rate versus level function was significantly affected by the temporal characteristics of the noise masker. Simultaneously gated noise caused higher baseline responses and greater dynamic range compression compared with noise distribution. The slopes of psychometric and neurometric functions were significantly shallower for higher variance distributions, suggesting that neuronal sensitivity might change with the variability of the sound. Our results suggest that the adaptive response of IC neurons to sound regularities does not affect the effectiveness of the noise-masking signal, which remains invariant to surrounding noise amplitudes. NEW & NOTEWORTHY Auditory neurons adapt to the statistics of sound levels in the acoustic scene. However, it is still unclear to what extent such adaptation influences the effectiveness of the stimulus as a masker. Our study represents the first attempt to investigate how the adaptation to the statistics of masking stimuli may be related to the effectiveness of masking, and to the single-unit encoding of the midbrain auditory neurons in behaving animals.

Tactile Masking by Electrovibration.

Future touch screen applications will include multiple tactile stimuli displayed simultaneously or consecutively to single finger or multiple fingers. These applications should be designed by considering human tactile masking mechanism since it is known that presenting one stimulus may interfere with the perception of the other. In this study, we investigate the effect of masking on the tactile perception of electrovibration displayed on touch screens. Through conducting psychophysical experiments with nine participants, we measured the masked thresholds of sinusoidal electrovibration bursts (125 Hz) under two masking conditions: simultaneous and pedestal. The masking signals were noise bursts, applied at five different sensation levels varying from 2 to 22 dB SL, also presented by electrovibration. For each participant, the thresholds were elevated as linear functions of masking levels for both masking types. We observed that the masking effectiveness was larger with pedestal masking than simultaneous masking. Moreover, in order to investigate the effect of tactile masking on our haptic perception of edge sharpness, we compared the perceived sharpness of edges separating two textured regions displayed with and without various types of masking stimuli. Our results suggest that sharpness perception depends on the local contrast between background and foreground stimuli, which varies as a function of masking amplitude and activation levels of frequency-dependent psychophysical channels.

Spatial Attention Enhances the Neural Representation of Invisible Signals Embedded in Noise.

Recent evidence suggests that voluntary spatial attention can affect neural processing of visual stimuli that do not enter conscious awareness (i.e., invisible stimuli), supporting the notion that attention and awareness are dissociable processes [Wyart, V., Dehaene, S., & Tallon-Baudry, C. Early dissociation between neural signatures of endogenous spatial attention and perceptual awareness during visual masking. Frontiers in Human Neuroscience, 6, 1-14, 2012; Watanabe, M., Cheng, K., Murayama, Y., Ueno, K., Asamizuya, T., Tanaka, K., et al. Attention but not awareness modulates the BOLD signal in the human V1 during binocular suppression. Science, 334, 829-831, 2011]. To date, however, no study has demonstrated that these effects reflect enhancement of the neural representation of invisible stimuli per se, as opposed to other neural processes not specifically tied to the stimulus in question. In addition, it remains unclear whether spatial attention can modulate neural representations of invisible stimuli in direct competition with highly salient and visible stimuli. Here we developed a novel EEG frequency-tagging paradigm to obtain a continuous readout of human brain activity associated with visible and invisible signals embedded in dynamic noise. Participants ( n = 23) detected occasional contrast changes in one of two flickering image streams on either side of fixation. Each image stream contained a visible or invisible signal embedded in every second noise image, the visibility of which was titrated and checked using a two-interval forced-choice detection task. Steady-state visual-evoked potentials were computed from EEG data at the signal and noise frequencies of interest. Cluster-based permutation analyses revealed significant neural responses to both visible and invisible signals across posterior scalp electrodes. Control analyses revealed that these responses did not reflect a subharmonic response to noise stimuli. In line with previous findings, spatial attention increased the neural representation of visible signals. Crucially, spatial attention also increased the neural representation of invisible signals. As such, the present results replicate and extend previous studies by demonstrating that attention can modulate the neural representation of invisible signals that are in direct competition with highly salient masking stimuli.

Motion-induced compression of perceived numerosity

It has been recently proposed that space, time, and number might share a common representation in the brain. Evidence supporting this idea comes from adaptation studies demonstrating that prolonged exposure to a given stimulus feature distorts the perception of different characteristics. For example, visual motion adaptation affects both perceived position and duration of subsequent stimuli presented in the adapted location. Here, we tested whether motion adaptation also affects perceived numerosity, by testing the effect of adaptation to translating or rotating stimuli moving either at high (20 Hz) or low (5 Hz) speed. Adaptation to fast translational motion yielded a robust reduction in the apparent numerosity of the adapted stimulus (~25%) while adaptation to slow translational or circular motion (either 20 Hz or 5 Hz) yielded a weaker but still significant compression. Control experiments suggested that none of these results could be accounted for in terms of stimulus masking. Taken together, our results are consistent with the extant literature supporting the idea of a generalized magnitude system underlying the representation of numerosity, space and time via common metrics. However, as changes in perceived numerosity co-varied with both adapting motion profile and speed, our evidence also suggests complex and asymmetric interactions between different magnitude representations.