Search

A salient color distractor is known to capture attention during search for a less salient shape target, but the mechanisms underlying attentional capture are debated. Theeuwes (2004, Psychonomic Bulletin & Review, 11(1), 65–70) argued that attentional capture depends on the size of the attentional window. If the attentional window is large, search is efficient and attentional capture should be stronger because the distractor is more likely to be inside the window. Consistently, we found higher search efficiency and more attentional capture in singleton than in feature search. However, differences in attentional capture only occurred when singleton and feature search were performed by different groups of participants, but not when singleton and feature search occurred unpredictably in the same group of participants. This result contradicts the attentional window account because search efficiency was always higher in singleton than in feature search. Rather, the results support search mode theory, which claims that participants looked for the most salient stimulus in singleton search ("singleton detection mode"), which resulted in more capture by the salient color distractor. When search types varied unpredictably, it was impossible to apply a consistent search strategy, which eliminated the differences between singleton and feature search. Further, we manipulated search efficiency by target–nontarget similarity. With dissimilar nontargets, the target was salient and search efficiency was high. Therefore, the attentional window account predicts more capture. However, we found the opposite result in singleton search and no difference in feature search. Taken together, these observations are inconsistent with the attentional window account but support search mode theory. [ABSTRACT FROM AUTHOR]

There has been a long-lasting debate about whether salient stimuli, such as uniquely colored objects, have the ability to automatically distract us. To resolve this debate, it has been suggested that salient stimuli do attract attention but that they can be suppressed to prevent distraction. Some research supporting this viewpoint has focused on a newly discovered ERP component called the distractor positivity (PD), which is thought to measure an inhibitory attentional process. This collaborative review summarizes previous research relying on this component with a specific emphasis on how the PD has been used to understand the ability to ignore distracting stimuli. In particular, we outline how the PD component has been used to gain theoretical insights about how search strategy and learning can influence distraction. We also review alternative accounts of the cognitive processes indexed by the PD component. Ultimately, we conclude that the PD component is a useful tool for understanding inhibitory processes related to distraction and may prove to be useful in other areas of study related to cognitive control. [ABSTRACT FROM AUTHOR]

In visual search tasks, negative features provide information about stimuli that can be excluded from search. It has been shown that these negative features help participants to locate the target, possibly by attentional suppression of stimuli sharing the negative feature. Attentional suppression is assumed to be reflected in an event-related potential, the PD component. To provide a further test of these assumptions, we presented the color of the distractor at the start of a trial and asked participants to find the other colored stimulus in the subsequent search display. Consistent with attentional suppression, we observed a PD to a lateral distractor shown with a vertical target. However, the PD occurred in this condition only when target and distractor could also be on opposite sides of fixation. The effect of trial context on the PD suggests that the PD reflects a search strategy whereby participants select stimuli opposite to the distractor when trials with opposite placements occur during the experiment. Therefore, the PD to the distractor may in fact be an N2pc to the opposite stimulus, indicating that the distractor is not suppressed, but avoided by redirecting attentional selection to the opposite side. [ABSTRACT FROM AUTHOR]

Visual attention is often inadvertently captured by salient stimuli. It was suggested that it is possible to prevent attentional capture in some search tasks by suppressing salient stimuli below baseline. Evidence for attentional suppression comes from a probe task that was interleaved with the main search task. In the probe task of Gaspelin et al. (Psychol Sci 26(11):1740–1750, 2015. https://doi.org/10.1177/0956797615597913), letters were shown on the stimuli of the search display and participants had to identify as many letters as possible. Performance was found to be worse for letters shown on the distractor compared to non-salient non-target stimuli, suggesting that distractor processing was suppressed below baseline. However, it is unclear whether suppression occurred at the level of perception or decision-making because participants may have reported letters on the distractor less frequently than letters on nontargets. This decision-level bias may have degraded performance for letters on distractor compared to nontarget stimuli without changing perception. After replicating the original findings, we conducted two experiments where we avoided report bias by cueing only a single letter for report. We found that the difference between distractor and nontarget stimuli was strongly reduced, suggesting that decision-level processes contribute to attentional suppression. In contrast, the difference between target and non-target stimuli was unchanged, suggesting that it reflected perceptual-level enhancement of the target stimuli. [ABSTRACT FROM AUTHOR]

In visual search tasks, salient distractors may capture attention involuntarily, but interference can be reduced when the salient distractor appears more frequently on one out of several possible positions. The reduction was attributed to attentional suppression of the high-probability position. However, all previous studies on this topic compared performance on the high-probability position to the remaining positions, which had a low probability of containing the distractor. Therefore, it is not clear whether the difference resulted from reduced interference on the high-probability position or from increased interference on the low-probability positions. To decide between these alternatives, we compared high-probability and low-probability with equal-probability positions. Consistent with attentional suppression, interference was reduced on the high-probability position compared with equal-probability positions. However, there was also an increase in interference on low-probability positions compared with equal-probability positions. The increase is in line with previous reports of boosted interference when distractors are rare. Our results show that the experimental design used in previous research is insufficient to separate effects of attentional suppression and those of distractor rarity. [ABSTRACT FROM AUTHOR]

The biased competition account claims that competition between two stimuli increases when they are close together compared with when they are far apart. The reason is that nearby stimuli are more likely to be represented in the same receptive fields, requiring top–down or bottom–up biases to resolve the ambiguity. Consistent with biased competition, previous research showed that an index of attentional enhancement, the N2pc component, was attenuated when two targets were close together. In contrast, it is unclear whether distractor processing would also be attenuated when the distractor is close to the target. To answer this question, we used the additional singleton paradigm where a target is sometimes accompanied by a more salient, but entirely irrelevant, distractor. In the conditions of interest, the distance between the target and the distractor was systematically manipulated whereas the eccentricity to central fixation was always the same. The results showed that two indices of attentional suppression, the positivity posterior contralateral and distractor positivity components, were attenuated when the distractor was close to the target. Consistent with biased competition, attentional suppression of distractors was inhibited when the distance between target and distractor was short. The reduced attentional suppression of distractors with nearby targets may contribute to the increased behavioral interference with close distractors. [ABSTRACT FROM AUTHOR]

Visual selection of target objects relies on representations of their known features in visual working memory. These representations are referred to as attentional templates. We asked how the capacity of visual working memory relates to the maximal number of attentional templates that can simultaneously guide visual selection. To measure the number of active attentional templates, we used the contingent capture paradigm where cues matching the attentional template have larger effects than cues in a non-matching color. We found larger cueing effects for matching than non-matching cues in one-, two-, and also three-color searches, suggesting that participants can establish up to three attentional templates. However, scrutiny of matching cue trials showed that with three attentional templates, larger cueing effects only occurred when the matching cue had the same color as the actual target. When the matching cue had a possible target color that was different from the actual target color, cueing effects were similar to non-matching cue colors. We assume that processing of a matching cue activates one of the three templates, which inhibits the remaining templates to the level of non-matching colors. With two colors, the inhibition from the activated template is less complete because the initial template activation is higher. Overall, only a maximum of two attentional templates can operate successfully in the contingent capture paradigm. The capacity of template-guided search is therefore far below the capacity of visual working memory. [ABSTRACT FROM AUTHOR]

Recently, working memory (WM) has been conceptualized as a limited resource, distributed flexibly and strategically between an unlimited number of representations. In addition to improving the precision of representations in WM, the allocation of resources may also shape how these representations act as attentional templates to guide visual search. Here, we reviewed recent evidence in favor of this assumption and proposed three main principles that govern the relationship between WM resources and template-guided visual search. First, the allocation of resources to an attentional template has an effect on visual search, as it may improve the guidance of visual attention, facilitate target recognition, and/or protect the attentional template against interference. Second, the allocation of the largest amount of resources to a representation in WM is not sufficient to give this representation the status of attentional template and thus, the ability to guide visual search. Third, the representation obtaining the status of attentional template, whether at encoding or during maintenance, receives an amount of WM resources proportional to its relevance for visual search. Thus defined, the resource hypothesis of visual search constitutes a parsimonious and powerful framework, which provides new perspectives on previous debates and complements existing models of template-guided visual search. [ABSTRACT FROM AUTHOR]

People's eyes are directed at objects of interest with the aim of acquiring visual information. However, processing this information is constrained in capacity, requiring task-driven and salience-driven attentional mechanisms to select few among the many available objects. A wealth of behavioral and neurophysiological evidence has demonstrated that visual selection and the motor selection of saccade targets rely on shared mechanisms. This coupling supports the premotor theory of visual attention put forth more than 30 years ago, postulating visual selection as a necessary stage in motor selection. In this review, we examine to which extent the coupling of visual and motor selection observed with saccades is replicated during ocular tracking. Ocular tracking combines catch-up saccades and smooth pursuit to foveate a moving object. We find evidence that ocular tracking requires visual selection of the speed and direction of the moving target, but the position of the motion signal may not coincide with the position of the pursuit target. Further, visual and motor selection can be spatially decoupled when pursuit is initiated (open-loop pursuit). We propose that a main function of coupled visual and motor selection is to serve the coordination of catch-up saccades and pursuit eye movements. A simple race-to-threshold model is proposed to explain the variable coupling of visual selection during pursuit, catch-up and regular saccades, while generating testable predictions. We discuss pending issues, such as disentangling visual selection from preattentive visual processing and response selection, and the pinpointing of visual selection mechanisms, which have begun to be addressed in the neurophysiological literature. [ABSTRACT FROM AUTHOR]

In visual search, the internal representation of the target feature is referred to as the attentional template. The attentional template can be broad or precise depending on the task requirements. In singleton search, the attentional template is broad because the target is the only colored element in the display. In feature search, a precise attentional template is required because the target is in a specific color in an array of varied colors. To measure the precision of the attentional template, we used a cue-target paradigm where cueing benefits decrease when the cue color differs from the target color. Consistent with broad and precise attentional templates, the decrease of cueing effects was stronger in feature than in singleton search. Measurements of ERPs showed that the N2pc elicited by the cue decreased with increasing color difference, suggesting that attention was more strongly captured by cues that were similar to the target. However, the cue-elicited N2pc did not differ between feature and singleton search, making it unlikely to reflect the mechanism underlying attentional template precision. Furthermore, there was no evidence for attentional suppression as there was no cue-elicited PD, even in conditions where the cueing benefit turned into a same-location cost. However, an index of signal enhancement, the contralateral positivity, reflected attention template precision. In general, there was sensory enhancement of the stimulus appearing at the cued location in the search display. With broad attentional templates, any stimulus at the cued location was enhanced, whereas enhancement was restricted to target-matching colors with precise attentional templates. [ABSTRACT FROM AUTHOR]

Visual search may be disrupted by the presentation of salient, but irrelevant stimuli. To reduce the impact of salient distractors, attention may suppress their processing below baseline level. While there are many studies on the attentional suppression of distractors with features distinct from the target (e.g., a color distractor with a shape target), there is little and inconsistent evidence for attentional suppression with distractors sharing the target feature. In this study, distractor and target were temporally separated in a cue–target paradigm, where the cue was shown briefly before the target display. With target-matching cues, RTs were shorter when the cue appeared at the target location (valid cues) compared with when it appeared at a nontarget location (invalid cues). To induce attentional suppression, we presented the cue more frequently at one out of four possible target positions. We found that invalid cues appearing at the high-frequency cue position produced less interference than invalid cues appearing at a low-frequency cue position. Crucially, target processing was also impaired at the high-frequency cue position, providing strong evidence for attentional suppression of the cued location. Overall, attentional suppression of the frequent distractor location could be established through feature-based attention, suggesting that feature-based attention may guide attentional suppression just as it guides attentional enhancement. [ABSTRACT FROM AUTHOR]

Even in sparse visual environments, observers may not be able to report features of objects they have just encountered in a surprise question. Attribute amnesia and seeing without knowing describe report failures for irrelevant features of objects that have been processed to some extent in the primary task. Both phenomena are attributed to the exclusive selection of relevant information for memory consolidation or for awareness, respectively. While attribute amnesia was found even for irrelevant attributes of the target in the primary task, seeing without knowing was not observed when a single object was presented foveally. To elucidate this discrepancy, we examined report failures for irrelevant attributes of single target objects, which were presented either in the fovea or in the periphery, and either at cued or uncued locations. On a surprise trial, observers were able to report the irrelevant shape and color of the target object when it was presented foveally. However, presenting the same object just slightly away from the fovea led to report failures for shape. Introducing a valid peripheral cue prior to target presentation reduced report failures for shape when the cue was predictive of the target location, suggesting that the pre-allocation of endogenous spatial attention promoted the processing of irrelevant shape information. In accordance with previous research, we suggest that these modulations are due to differences in late selection for conscious awareness or consolidation in working memory. [ABSTRACT FROM AUTHOR]

Top–down control of attention allows us to resist attentional capture by salient stimuli that are irrelevant to our current goals. Recently, it was proposed that attentional suppression of salient distractors contributes to top–down control by biasing attention away from the distractor. With small search displays, attentional suppression of salient distractors may even result in reduced RTs on distractor-present trials. In support of attentional suppression, electrophysiological measures revealed a positivity between 200 and 300 msec contralateral to the distractor, which has been referred to as distractor positivity (PD). We reexamined distractor benefits with small search displays and found that the positivity to the distractor was followed by a negativity to the distractor. The negativity, referred to as N2pc, is considered an index of attentional selection of the contralateral element. Thus, attentional suppression of the distractor (PD) preceded attentional capture (N2pc) by the distractor, which is at odds with the idea that attentional suppression avoids attentional capture by the distractor. Instead, we suggest that the initial "PD" is not a positivity to the distractor but rather a negativity (N2pc) to the contralateral context element, suggesting that, initially, the context captured attention. Subsequently, the distractor was selected because, paradoxically, participants searched all lateral target positions (even when irrelevant) before they examined the vertical positions. Consistent with this idea, search times were shorter for lateral than vertical targets. In summary, the early voltage difference in small search displays is unrelated to distractor suppression but may reflect capture by the context. [ABSTRACT FROM AUTHOR]

Earlier research suggested that gaze direction has an impact on cognitive processing. It is likely that horizontal gaze direction increases activation in specific areas of the contralateral cerebral hemisphere. Consistent with the lateralization of memory functions, we previously showed that shifting gaze to the left improves visuo-spatial short-term memory. In the current study, we investigated the effect of unilateral gaze on verbal processing. We expected better performance with gaze directed to the right because language is lateralized in the left hemisphere. Also, an advantage of gaze directed upward was expected because local processing and object recognition are facilitated in the upper visual field. Observers directed their gaze at one of the corners of the computer screen while they performed lexical decision, grammatical gender and semantic discrimination tasks. Contrary to expectations, we did not observe performance differences between gaze directed to the left or right, which is consistent with the inconsistent literature on horizontal asymmetries with verbal tasks. However, RTs were shorter when observers looked at words in the upper compared to the lower part of the screen, suggesting that looking upwards enhances verbal processing. [ABSTRACT FROM AUTHOR]

Gaspelin and Luck describe the signal suppression hypothesis, which proposes that attentional suppression prevents the capture of visual attention by salient distractors. We will discuss several problems with this proposal. On a theoretical level, we will argue that attentional suppression is a dispensable mechanism. Most effects of attentional suppression can be easily explained by reduced target expectancy at the distractor location. On an empirical level, we will argue that electrophysiological evidence for attentional suppression is spurious because, in key conditions, the PD most likely reflects idiosyncratic scan paths. [ABSTRACT FROM AUTHOR]

The threat capture hypothesis states that threatening stimuli are automatically processed with higher priority than non-threatening stimuli, irrespective of observer intentions or focus of attention. We evaluated the threat capture hypothesis with respect to the early perceptual stages of face processing. We focused on an electrophysiological marker of face processing (the lateralized N170) in response to neutral, happy, and angry facial expressions displayed in competition with a non-face stimulus (a house). We evaluated how effects of facial expression on the lateralized N170 were modulated by task demands. In the pixel task, participants were required to identify the gender of the face, which made the face task-relevant and entailed structural encoding of the face stimulus. In the pixel task, participants identified the location of a missing pixel in the fixation cross, which made the face task-irrelevant and placed it outside the focus of attention. When faces were relevant, the lateralized N170 to angry faces was enhanced compared to happy and neutral faces. When faces were irrelevant, facial expression had no effect. These results reveal the critical role of task demands on the preference for threatening faces, indicating that top-down, voluntary processing modulates the prioritization of threat. [ABSTRACT FROM AUTHOR]

When people are required to indicate the vanishing location of a moving object, systematic biases forward, in the direction of motion, and downward, in the direction of gravity, are usually found. Both these displacements, called representational momentum and representational gravity, respectively, are thought to reflect anticipatory internal mechanisms aiming to overcome neural delays in the perception of motion. We challenge this view. There may not be such a single mechanism. Although both representational momentum and representational gravity follow a specific time-course, compatible with an anticipation of the object's dynamics, they do not seem to be commensurable with each other, as they are differentially modulated by relevant variables, such as eye movements and strength of motion signals. We found separate response components, one related to overt motor localization behaviour and one limited to purely perceptual judgement. Representational momentum emerged only for the motor localization task, revealing a motor overshoot. In contrast, representational gravity was mostly evident for spatial perceptual judgements. We interpret the results in support of a partial dissociation in the mechanisms that give rise to representational momentum and representational gravity, with the former but not the latter strongly modulated by the enrolment of the motor system. [ABSTRACT FROM AUTHOR]

Smooth pursuit eye movements (pursuit) are used to minimize the retinal motion of moving objects. During pursuit, the pattern of motion on the retina carries not only information about the object movement but also reafferent information about the eye movement itself. The latter arises from the retinal flow of the stationary world in the direction opposite to the eye movement. To extract the global direction of motion of the tracked object and stationary world, the visual system needs to integrate ambiguous local motion measurements (i.e., the aperture problem). Unlike the tracked object, the stationary world's global motion is entirely determined by the eye movement and thus can be approximately derived from motor commands sent to the eye (i.e., from an efference copy). Because retinal motion opposite to the eye movement is dominant during pursuit, different motion integration mechanisms might be used for retinal motion in the same direction and opposite to pursuit. To investigate motion integration during pursuit, we tested direction discrimination of a brief change in global object motion. The global motion stimulus was a circular array of small static apertures within which one-dimensional gratings moved. We found increased coherence thresholds and a qualitatively different reflexive ocular tracking for global motion opposite to pursuit. Both effects suggest reduced sampling of motion opposite to pursuit, which results in an impaired ability to extract coherence in motion signals in the reafferent direction. We suggest that anisotropic motion integration is an adaptation to asymmetric retinal motion patterns experienced during pursuit eye movements. NEW & NOTEWORTHY This study provides a new understanding of how the visual system achieves coherent perception of an object's motion while the eyes themselves are moving. The visual system integrates local motion measurements to create a coherent percept of object motion. An analysis of perceptual judgments and reflexive eye movements to a brief change in an object's global motion confirms that the visual and oculomotor systems pick fewer samples to extract global motion opposite to the eye movement. [ABSTRACT FROM AUTHOR]

According to the threat-capture hypothesis, irrelevant-but-salient stimuli interfere more with a visual search task when they are perceived as threatening. We investigated the neural basis for behavioural interference in conditions that promote attentional suppression of distracting stimuli (i.e., easy search with predictable targets). In Experiment 1, participants discriminated the shape of a neutral target (a flower), which competed for selection with a threat-related or neutral distractor (spider or leaf, respectively). In line with prior results, we observed larger behavioural interference from spider than leaf distractors. Electrophysiological recordings revealed a posterior positivity between 200 and 300 ms, the PD, suggesting that participants actively suppressed both leaf and spider distractors. Critically, the PD was delayed with spider compared to leaf distractors. Experiment 2 was a control experiment where we confirmed that the results depended on the execution of the peripheral search task. When participants performed a localization task on the fixation cross, the decisive results from Experiment 1 were not replicated despite equal peripheral stimulation. Our results indicate that the behavioural delay incurred by threatening stimuli is accompanied by a delay of suppressive mechanisms. Conversely, we found no evidence for initial capture followed by suppression that may be predicted by hypervigilance-avoidance theory. [ABSTRACT FROM AUTHOR]

Salient vocalizations, especially aggressive voices, are believed to attract attention due to an automatic threat detection system. However, studies assessing the temporal dynamics of auditory spatial attention to aggressive voices are missing. Using event-related potential markers of auditory spatial attention (N2ac and LPCpc), we show that attentional processing of threatening vocal signals is enhanced at two different stages of auditory processing. As early as 200 ms post-stimulus onset, attentional orienting/engagement is enhanced for threatening as compared to happy vocal signals. Subsequently, as early as 400 ms post-stimulus onset, the reorienting of auditory attention to the center of the screen (or disengagement from the target) is enhanced. This latter effect is consistent with the need to optimize perception by balancing the intake of stimulation from left and right auditory space. Our results extend the scope of theories from the visual to the auditory modality by showing that threatening stimuli also bias early spatial attention in the auditory modality. Attentional enhancement was only present in female and not in male participants. [ABSTRACT FROM AUTHOR]

Abstract: Inhibition of return is the name typically given to the prolonged latency of motor responses directed to a previously cued target location. There is intense debate about the origins of this effect and its function, but most take for granted (despite lack of evidence) that it depends little on forward masking. Therefore, we re-examined the role of forward masking in inhibition of return. Forward masking was indexed by slower saccadic reaction times (SRTs) when the target orientation repeated the cue orientation at the same location. We confirmed effects of orientation repetition in the absence of an attentional bias when cues were presented on both sides of fixation (bilateral presentation). The effect of orientation repetition was reduced with high target contrast, consistent with a low-level origin such as contrast gain control in early visual areas. When presenting cues on only one side of fixation (unilateral presentation), we obtained inhibition of return with longer cue-target intervals and facilitation with targets presented shortly after the cue. The effect of orientation repetition was reduced when facilitation was observed, but was as strong as with bilateral cues when inhibition of return was observed. Therefore, forward masking may contribute to the inhibition of return effect by delaying reaction times to repeated features at the same location, but is not a principal cause of inhibition of return; in agreement with previous views.Significance statement: The saccadic inhibition of return effect is a reaction-time cost when responding to a pre-cued location. Additional object updating costs are typically invoked to explain reaction-time costs observed when cue and target have the same shape. Yet, lower-level, forward masking of the target by the cue can not be ruled out. Importantly, we show an effect of orientation repetition that is consistent with low-level forward masking rather than object updating costs and that does not interact with inhibition of return. [ABSTRACT FROM AUTHOR]

The orientation-bias hypothesis states that there is a bias to attend to the right visual hemifield (RVF) when there is spatial competition between stimuli in the left and right hemifield [Pollmann, S. (1996). A pop-out induced extinction-like phenomenon in neurologically intact subjects. Neuropsychologia, 34(5), 413- 425. doi:10.1016/0028-3932(95)00125-5]. In support of this hypothesis, stronger interference was reported for RVF distractors with contralateral targets. In contrast, previous studies using rapid serial visual presentation (RSVP) found stronger interference from distractors in the left visual hemifield (LVF). We used the additional singleton paradigm to test whether this discrepancy was due to the different distractor features that were employed (colour vs. orientation). Interference from the colour distractor with contralateral targets was larger in the RVF than in the LVF. However, the asymmetrical interference disappeared when observers had to search for an inconspicuous colour target instead of the inconspicuous shape target. We suggest that the LVF orienting-bias is limited to situations where search is driven by bottom-up saliency (singleton search) instead of top-down search goals (feature search). In contrast, analysis of the literature suggests the opposite for the LVF bias in RSVP tasks. Thus, the attentional asymmetry may depend on whether the task involves temporal or spatial competition, and whether search is based on bottom-up or top-down signals. [ABSTRACT FROM AUTHOR]

Search for a shape target is difficult when its shape is similar to the shape of the surrounding nontargets and easy when it is dissimilar. We asked whether interference from a salient but irrelevant color singleton depended on search difficulty as manipulated by target-nontarget similarity. We found that interference was strong in difficult searches, and the occurrence of an electrophysiological index of attentional selectivity (the N2pc component) confirmed that attention was captured by the distractor. In contrast, interference from the distractor was weak with easy searches, and the occurrence of the PD component confirmed that saliency signals from the distractor were suppressed. The results suggest that attentional suppression of salient but irrelevant distractors is only possible when search is efficient (i.e., with low target-nontarget similarity), otherwise, attentional capture occurs. Further, we analyzed the Ppc component, a positivity occurring between 100 and 200 ms after stimulus onset contralateral to a salient feature discontinuity. It has been suggested that the Ppc reflects bottom-up saliency signals, but we found the Ppc to occur only when the salient stimulus was unlikely to be selected, as in efficient searches. Thus, attentional requirements modulate the Ppc component. [ABSTRACT FROM AUTHOR]

Some points of criticism against the idea that attentional selection is controlled by bottom-up processing were dispelled by the attentional window account. The attentional window account claims that saliency computations during visual search are only performed for stimuli inside the attentional window. Therefore, a small attentional window may avoid attentional capture by salient distractors because it is likely that the salient distractor is located outside the window. In contrast, a large attentional window increases the chances of attentional capture by a salient distractor. Large and small attentional windows have been associated with efficient (parallel) and inefficient (serial) search, respectively. We compared the effect of a salient color singleton on visual search for a shape singleton during efficient and inefficient search. To vary search efficiency, the nontarget shapes were either similar or dissimilar with respect to the shape singleton. We found that interference from the color singleton was larger with inefficient than efficient search, which contradicts the attentional window account. While inconsistent with the attentional window account, our results are predicted by computational models of visual search. Because of target-nontarget similarity, the target was less salient with inefficient than efficient search. Consequently, the relative saliency of the color distractor was higher with inefficient than with efficient search. Accordingly, stronger attentional capture resulted. Overall, the present results show that bottom-up control by stimulus saliency is stronger when search is difficult, which is inconsistent with the attentional window account. [ABSTRACT FROM AUTHOR]

We tested whether two known hemi-field asymmetries would affect visual search with face stimuli. Holistic processing of spatial configurations is better in the left hemi-field, reflecting a right hemisphere specialization, and object recognition is better in the upper visual field, reflecting stronger projections into the ventral stream. Faces tap into holistic processing and object recognition at the same time, which predicts better performance in the left and upper hemifield, respectively. In the first experiment, participants had to detect a face with a gaze direction different from the remaining faces. Participants were faster to respond when targets were presented in the left and upper hemi-field. The same pattern of results was observed when only the eye region was presented. In the second experiment, we turned the faces upside-down, which eliminated the typical spatial configuration of faces. The left hemi-field advantage disappeared, showing that it is related to holistic processing of faces, whereas the upper hemifield advantage related to object recognition persisted. Finally, we made the search task easier by asking observers to search for a face with open among closed eyes or vice versa. The easy search task eliminated the need for complex object recognition and, accordingly, the advantage of the upper visual field disappeared. Similarly, the left hemi-field advantage was attenuated. In sum, our findings show that both horizontal and vertical asymmetries affect the search for faces and can be selectively suppressed by changing characteristics of the stimuli. [ABSTRACT FROM AUTHOR]

Most theories of visual search maintain that attention is selectively tuned to the attributes of the search target (e.g., orange). Conversely, according to the relational account, attention is biased to the relative feature of the target (e.g., redder). However, previous studies that supported the relational account mainly measured mean response times. Hence, the results might not reflect early, perceptual mechanisms (e.g., signal enhancement) but later, decision-based mechanisms (channel selection). The current study tested the relational account against feature-specific theories in a spatial cueing task, in which the targets were backward-masked, and target identification accuracy was measured. The first experiment corroborated earlier results, demonstrating that relational effects are due to signal enhancement. In the second experiment, we chose highly discriminable colours along the blue-red continuum, and obtained results that were more consistent with broad feature-specific rather than relational tuning. The implications of these findings for current theories of attention are discussed. [ABSTRACT FROM AUTHOR]

We are faster and more accurate at detecting frequently occurring objects than infrequent ones, just as we are faster and more accurate at detecting objects that have been spatially cued. Does this behavioral similarity reflect similar processes? To evaluate this question we manipulated orientation probability and exogenous spatial cuing within a single perceptual estimation task. Both increased target probability and spatial cuing led to shorter response initiation times and more precise perceptual reports, but these effects were additive. Further, target probability changed the shape of the distribution of errors while spatial cuing did not. Different routes and independent mechanisms could lead to changes in behavioral measures that look similar to each other and to 'attentional' effects. [ABSTRACT FROM AUTHOR]

Peripheral cues reduce reaction times (RTs) to targets at the cued location with short cue-target SOAs (cueing benefits) but increase RTs at long SOAs (cueing costs or inhibition of return). In detection tasks, cueing costs occur at shorter SOAs and are larger compared with identification tasks. To account for effects of task, detection cost theory claims that the integration of cue and target into an object file makes it more difficult to detect the target as a new event, which is the principal task-requirement in detection tasks. The integration of cue and target is expected to increase when cue and target are similar. We provided evidence for detection cost theory in the modified spatial cueing paradigm. Two types of cues (onset, color) were paired with two types of targets (onset, color) in separate blocks of trials. In the identification task, we found cueing benefits with matching (i.e., similar) cue-target pairs (onset-onset, color-color) and no cueing effects with nonmatching cue-target pairs (onset-color, color-onset), which replicates previous work. In the detection task, cueing effects with matching cues were reduced and even turned into cueing costs for onset cues with onset targets, suggesting that cue-target integration made it more difficult to detect targets at the cued location as new events. In contrast, the results for nonmatching cue-target pairs were not affected by task. Furthermore, the pattern of false alarms in the detection task provides a measure of similarity that may explain the size of cueing benefits and costs. [ABSTRACT FROM AUTHOR]

Gaze is one of the most important cues for human communication and social interaction. In particular, gaze contact is the most primary form of social contact and it is thought to capture attention. A very early-differentiated brain response to direct versus averted gaze has been hypothesized. Here, we used high-density electroencephalography to test this hypothesis. Topographical analysis allowed us to uncover a very early topographic modulation (40–80 ms) of event-related responses to faces with direct as compared to averted gaze. This modulation was obtained only in the condition where intact broadband faces–as opposed to high-pass or low-pas filtered faces–were presented. Source estimation indicated that this early modulation involved the posterior parietal region, encompassing the left precuneus and inferior parietal lobule. This supports the idea that it reflected an early orienting response to direct versus averted gaze. Accordingly, in a follow-up behavioural experiment, we found faster response times to the direct gaze than to the averted gaze broadband faces. In addition, classical evoked potential analysis showed that the N170 peak amplitude was larger for averted gaze than for direct gaze. Taken together, these results suggest that direct gaze may be detected at a very early processing stage, involving a parallel route to the ventral occipito-temporal route of face perceptual analysis. [ABSTRACT FROM AUTHOR]

Our ability to select task-relevant information from cluttered visual environments is widely believed to be due to our ability to tune attention to the particular elementary feature values of a sought-after target (e.g., red, orange, yellow). By contrast, recent findings showed that attention is often tuned to feature relationships, that is, features that the target has relative to irrelevant features in the context (e.g., redder, yellower). However, the evidence for such a relational account is so far exclusively based on behavioral measures that do not allow a safe inference about early perceptual processes. The present study provides a critical test of the relational account, by measuring an electrophysiological marker in the EEG of participants (N2pc) in response to briefly presented distractors (cues) that could either match the physical features of the target or its relative features. In a first experiment, the target color and nontarget color were kept constant across trials. In line with a relational account, we found that only cues with the same relative color as the target were attended, regardless of whether the cues had the same physical color as the target. In a second experiment, we demonstrate that attention is biased to the exact target feature value when the target is embedded in a randomly varying context. Taken together, these results provide the first electrophysiological evidence that attention can modulate early perceptual processes differently; in a context-dependent manner versus a context-independent manner, resulting in marked differences in the range of colors that can attract attention. [ABSTRACT FROM AUTHOR]

It has been claimed that stimuli sharing the color of the nogo-target are suppressed because of the strong incentive to not process the nogo-target, but we failed to replicate this finding. Participants searched for a color singleton in the target display and indicated its shape when it was in the go color. If the color singleton in the target display was in the nogo color, they had to withhold the response. The target display was preceded by a cue display that also contained a color singleton (the cue). The cue was either in the color of the go or nogo target, or it was in an unrelated, neutral color. With cues in the go color, reaction times were shorter when the cue appeared at the same location as the target compared to when it appeared at a different location. Also, electrophysiological recordings showed that an index of attentional selection, the N2pc, was elicited by go cues. Surprisingly, we failed to replicate cueing costs for cues in the nogo color that were originally reported by Anderson and Folk (2012). Consistently, we also failed to find an electrophysiological index of attentional suppression (the PD) for cues in the nogo color. Further, fronto-central event-related potentials to the cue display showed the same negativity for nogo and neutral stimuli relative to go stimuli, which is at odds with response inhibition and conflict monitoring accounts of the Nogo-N2. Thus, the modified cueing paradigm employed here provides little evidence that features associated with nogo-targets are suppressed at the level of attention or response selection. Rather, nogo-stimuli are efficiently ignored and attention is focused on features that require a response. [ABSTRACT FROM AUTHOR]

Cerebral asymmetries and cortical regions associated with the upper and lower visual field were investigated using shifts of gaze. Earlier research suggests that gaze shifts to the left or right increase activation of specific areas of the contralateral hemisphere. We asked whether looking at one quadrant of the visual field facilitates the recall in various visuo-spatial tasks. The different components of visuo-spatial memory were investigated by probing memory for a stimulus matrix in each quadrant of the screen. First, memory for visual images or patterns was probed with a matrix of squares that was simultaneously presented and had to be reconstructed by mouse click. Better memory performance was found in the upper left quadrant compared to the three other quadrants indicating that both laterality and elevation are important. Second, positional memory was probed by subsequently presenting squares which prevented the formation of a visual image. Again, we found that gaze to the upper left facilitated performance. Third, memory for object-location binding was probed by asking observers to associate objects to particular locations. Higher performance was found with gaze directed to the lower quadrants irrespective of lateralization, confirming that only some components of visual short-term memory have shared neural substrates. [ABSTRACT FROM AUTHOR]

Involuntary ocular tracking responses to background motion offer a window on the dynamics of motion computations. In contrast to spatial attention, we know little about the role of feature-based attention in determining this ocular response. To probe feature-based effects of background motion on involuntary eye movements, we presented human observers with a balanced background perturbation. Two clouds of dots moved in opposite vertical directions while observers tracked a target moving in horizontal direction. Additionally, they had to discriminate a change in the direction of motion (± 10° from vertical) of one of the clouds. A vertical ocular following response occurred in response to the motion of the attended cloud. When motion selection was based on motion direction and color of the dots, the peak velocity of the tracking response was 30% of the tracking response elicited in a single task with only one direction of background motion. In two other experiments, we tested the effect of the perturbation when motion selection was based on color, by having motion direction vary unpredictably, or on motion direction alone. Although the gain of pursuit in the horizontal direction was significantly reduced in all experiments, indicating a trade-off between perceptual and oculomotor tasks, ocular responses to perturbations were only observed when selection was based on both motion direction and color. It appears that selection by motion direction can only be effective for driving ocular tracking when the relevant elements can be segregated before motion onset. [ABSTRACT FROM AUTHOR]

We investigated the effects of task demands and individual differences on the allocation of attention. Using the same stimuli, participants indicated the orientation of a line contained in a shape singleton (identification task) or the presence of singletons (detection task). Shape singletons in the identification task elicited a contralateral negativity ( N2pc) whereas shape singletons in the detection task elicited a contralateral positivity ( Pd). We suggest that the reduction of attentional priority of a salient stimulus, reflected by the Pd, occurred more rapidly with the less demanding detection task. Further, fewer distractible participants showed a larger N2pc to lateral color distractors than highly distractible participants. We suggest that highly distractible participants developed compensatory mechanisms to suppress distracting stimuli. [ABSTRACT FROM AUTHOR]

We tested whether color singletons lead to saccadic and manual inhibition of return (IOR; i.e., slower responses at cued locations) and whether IOR depended on the relevance of the color singletons. The target display was preceded by a nonpredictive cue display. In three experiments, half of the cues were response-relevant, because participants had to perform a discrimination task at the cued location. With the exception of Experiment 2, none of the cue colors matched the target color. We observed saccadic IOR after color singletons, which was greater for slow than for fast responses. Furthermore, when the relevant cue color matched the target color, we observed attentional capture (i.e., faster responses at cued locations) with rapid responses, but IOR with slower responses, which provides evidence for attentional deallocation. When the cue display was completely response-irrelevant in two additional experiments, we did not find evidence for IOR. Instead, we found attentional capture when the cue color matched the target color. Also, attentional capture was greater for rapid responses and with short cue–target intervals. Thus, IOR emerges when cues are relevant and do not match the target color, whereas attentional capture emerges with relevant and irrelevant cues that match the target color. [ABSTRACT FROM AUTHOR]

Reaction times in a visual search task increase when an irrelevant but salient stimulus is presented. Recently, the hypothesis that the increase in reaction times was due to attentional capture by the salient distractor has been disputed. We devised a task in which a search display was shown after observers had initiated a reaching movement toward a touch screen. In a display of vertical bars, observers had to touch the oblique target while ignoring a salient color singleton. Because the hand was moving when the display appeared, reach trajectories revealed the current selection for action. We observed that salient but irrelevant stimuli changed the reach trajectory at the same time as the target was selected, about 270 ms after movement onset. The change in direction was corrected after another 160 ms. In a second experiment, we compared manual selection of color and orientation targets and observed that selection occurred earlier for color than for orientation targets. Salient stimuli support faster selection than do less salient stimuli. Under the assumption that attentional selection for action and perception are based on a common mechanism, our results suggest that attention is indeed captured by salient stimuli. [ABSTRACT FROM AUTHOR]

We investigated localization performance of simple targets in patient TN, who suffered bilateral damage of his primary visual cortex and shows complete cortical blindness. Using a two-alternative forced-choice paradigm, TN was asked to guess the position of left-right targets with goal-directed and discrete manual responses. The results indicate a clear dissociation between goal-directed and discrete responses. TN pointed toward the correct target location in approximately 75% of the trials but was at chance level with discrete responses. This indicates that the residual ability to localize an unseen stimulus depends critically on the possibility to translate a visual signal into a goal-directed motor output at least in certain forms of blindsight. [ABSTRACT FROM AUTHOR]

Cortical blindness refers to the loss of vision that occurs after destruction of the primary visual cortex. Although there is no sensory cortex and hence no conscious vision, some cortically blind patients show amygdala activation in response to facial or bodily expressions of emotion. Here we investigated whether direction of gaze could also be processed in the absence of any functional visual cortex. A well-known patient with bilateral destruction of his visual cortex and subsequent cortical blindness was investigated in an fMRI paradigm during which blocks of faces were presented either with their gaze directed toward or away from the viewer. Increased right amygdala activation was found in response to directed compared with averted gaze. Activity in this region was further found to be functionally connected to a larger network associated with face and gaze processing. The present study demonstrates that, in human subjects, the amygdala response to eye contact does not require an intact primary visual cortex. [ABSTRACT FROM AUTHOR]

Attentional capture by salient distractors has been confirmed by the occurrence of an N2pc to the salient distractor. To clarify some failures to replicate this finding, we varied target predictability to induce different search modes. In the unpredictable target condition, the target shape varied randomly from trial to trial, favoring singleton detection mode. In the predictable target condition, the target shape remained the same in a block of trials, favoring feature search mode. With unpredictable targets, we observed an N2pc toward the salient color distractor, confirming attentional capture in singleton search mode. With predictable targets, there was no N2pc to the salient distractor, but a distractor positivity ( Pd), suggesting distractor suppression. Also, differences emerged in the topographic segmentation of N2pc and Pd. Further, the amplitude of the N2pc toward the target was larger with predictable than with unpredictable targets. [ABSTRACT FROM AUTHOR]

Approach-like actions are initiated faster with stimuli of positive valence. Conversely, avoidance-like actions are initiated faster with threatening stimuli of negative valence. We went beyond reaction time measures and investigated whether threatening stimuli also affect the way in which an action is carried out. Participants moved their hand either away from the picture of a spider (avoidance) or they moved their hand toward the picture of a spider (approach). We compared spider-fearful participants to non-anxious participants. When reaching away from the threatening spider picture, spider-fearful participants moved more directly to the target than controls. When reaching toward the threatening spider, spider-fearful participants moved less directly to the target than controls. Some conditions that showed clear differences in movement trajectories between spider-fearful and control participants were devoid of differences in reaction time. The deviation away from threatening stimuli provides evidence for the claim that affective states like fear leak into movement programming and produce deviations away from threatening stimuli in movement execution. Avoidance of threatening stimuli is rapidly integrated into ongoing motor behaviour in order to increase the distance between the participant's body and the threatening stimulus. [ABSTRACT FROM PUBLISHER]

Seeber (2011) recently introduced a series of analytical cognitive load models, providing a detailed illustration of conjectured cognitive resource allocation during simultaneous interpreting. In this article, the authors set out to compare these models with data gathered in an experiment using task-evoked pupillary responses to measure online cognitive load during simultaneous interpreting when embedded in single-sentence context and discourse context. Verb-final and verb-initial constructions were analysed in terms of the load they cause to an inherently capacity-limited system when interpreted simultaneously into a verb-initial language like English. The results show larger pupil dilation with verb-final than with verb-initial constructions, suggesting higher cognitive load with asymmetrical structures. A tendency for reduced cognitive load in the discourse context compared to the sentence context was also found. These data support the models’ prediction of an increase in cognitive load towards (and beyond) the end of verb-final constructions. [ABSTRACT FROM AUTHOR]

Numerous studies have suggested that the deployment of attention is linked to saliency. In contrast, very little is known about how salient objects are perceived. To probe the perception of salient elements, observers compared two horizontally aligned stimuli in an array of eight elements. One of them was salient because of its orientation or direction of motion. We observed that the perceived luminance contrast or color saturation of the salient element increased: the salient stimulus looked even more salient. We explored the possibility that changes in appearance were caused by attention. We chose an event-related potential indexing attentional selection, the N2pc, to answer this question. The absence of an N2pc to the salient object provides preliminary evidence against involuntary attentional capture by the salient element. We suggest that signals from a master saliency map flow back into individual feature maps. These signals boost the perceived feature contrast of salient objects, even on perceptual dimensions different from the one that initially defined saliency. [ABSTRACT FROM AUTHOR]

The current study investigated whether capture of the eyes by a salient onset distractor and the disengagement of the eyes from that distractor are driven by the same or by different underlying control modes. A variant of the classic oculomotor capture task was used. Observers had to make a saccade to the only gray circle among red background circles. On some trials, a green (novel color), red (placeholder color) or gray (target color) distractor square was presented with sudden onset. Results showed that when participants reacted fast, oculomotor capture was primarily driven by bottom-up pop-out: both types of distractors (green and gray) that popped out among the red background elements showed more capture than a red distractor that did not pop-out. In contrast to initial capture, disengagement of the eyes from the distractor was driven by top-down target-distractor similarity effects. We also examined the time-course of this effect. The distractor could change from green to either the target or placeholder color. When the color change was early in time (30-40 ms after its onset), dwell times were strongly affected by the change, whereas the effect on oculomotor capture was weak. Importantly, a change occurring as early as 60-80 ms after distractor onset did neither affect capture nor dwell times, corroborating the assumption of parallel programming of saccades. [ABSTRACT FROM AUTHOR]

It is known that visual transients prolong saccadic latency and reduce saccadic frequency. The latter effect was attributed to subcortical structures because it occurred only 60–70 ms after stimulus onset. We examined the effects of large task-irrelevant transients on steady-state pursuit and the generation of catch-up saccades. Two screen-wide stripes of equal contrast (4, 20, or 100%) were briefly flashed at equal eccentricities (3, 6, or 12°) from the pursuit target. About 100 ms after flash onset, we observed that pursuit gain dropped by 6–12% and catch-up saccades were entirely suppressed. The relatively long latency of the inhibition suggests that it results from cortical mechanisms that may act by promoting fixation or the deployment of attention over the visual field. In addition, we show that a loud irrelevant sound is able to generate the same inhibition of saccades as visual transients, whereas it only induces a weak modulation of pursuit gain, indicating a privileged access of acoustic information to the saccadic system. Finally, irrelevant changes in motion direction orthogonal to pursuit had a smaller and later inhibitory effect. [ABSTRACT FROM AUTHOR]

The Simon effect has most often been investigated with key-press responses and eye fixation. In the present study, we asked how the type of eye movement and the type of manual response affect response selection in a Simon task. We investigated three eye movement instructions (spontaneous, saccade, and fixation) while participants performed goal-directed (i.e., reaching) or symbolic (i.e., finger-lift) responses. Initially, no oculomotor constraints were imposed, and a Simon effect was present for both response types. Next, eye movements were constrained. Participants had to either make a saccade toward the stimulus or maintain gaze fixed in the screen centre. While a congruency effect was always observed in reaching responses, it disappeared in finger-lift responses. We suggest that the redirection of saccades from the stimulus to the correct response location in noncorresponding trials contributes to the Simon effect. Because of eye-hand coupling, this occurred in a mandatory manner with reaching responses but not with finger-lift responses. Thus, the Simon effect with key-presses disappears when participants do what they typically do-look at the stimulus. [ABSTRACT FROM AUTHOR]

After presentation of a peripheral cue, facilitation at the cued location is followed by inhibition of return (IOR). It has been recently proposed that IOR may originate at different processing stages for manual and ocular responses, with manual IOR resulting from inhibited attentional orienting, and ocular IOR resulting form inhibited motor preparation. Contrary to this interpretation, we found an effect of target contrast on saccadic IOR. The effect of contrast decreased with increasing reaction times (RTs) for saccades, but not for manual key-press responses. This may have masked the effect of contrast on IOR with saccades in previous studies (Hunt and Kingstone in J Exp Psychol Hum Percept Perform 29:1068–1074, ) because only mean RTs were considered. We also found that background luminance strongly influenced the effects of gap and target contrast on IOR. [ABSTRACT FROM AUTHOR]

Peripheral cues induce facilitation with short cue-target intervals and inhibition of return (IOR) with long cue-target intervals. Modulations of facilitation and IOR by continuous displacements of the eye or the cued stimuli are poorly understood. Previously, the retinal coordinates of the cued location were changed by saccadic or smooth pursuit eye movements during the cue-target interval. In contrast, we probed the relevant coordinates for facilitation and IOR by orthogonally varying object motion (stationary, moving) and eye movement (fixation, smooth pursuit). In the pursuit conditions, cue and target were presented during the ongoing eye movement and observers made a saccade to the target. Importantly, we found facilitation and IOR of similar size during smooth pursuit and fixation. The results suggest that involuntary orienting is possible even when attention has to be allocated to the moving target during smooth pursuit. Comparison of conditions with stabilized and moving objects suggest an oculocentric basis for facilitation as well as inhibition. Facilitation and IOR were reduced with objects that moved on the retina both with smooth pursuit and eye fixation. [ABSTRACT FROM AUTHOR]

During smooth pursuit eye movements, briefly presented objects are mislocalized in the direction of motion. It has been proposed that the localization error is the sum of the pursuit signal and the retinal motion signal in a ~200 ms interval after flash onset. To evaluate contributions of retinal motion signals produced by the entire object (global motion) and elements within the object (local motion), we asked observers to reach to flashed Gabor patches (Gaussian-windowed sine-wave gratings). Global motion was manipulated by varying the duration of a stationary flash, and local motion was manipulated by varying the motion of the sine-wave. Our results confirm that global retinal motion reduces the localization error. The effect of local retinal motion on object localization was far smaller, even though local and global motion had equal effects on eye velocity. Thus, local retinal motion has differential access to manual and oculomotor control circuits. Further, we observed moderate correlations between smooth pursuit gain and localization error. [ABSTRACT FROM AUTHOR]

When we view the world around us, we constantly move our eyes. This brings objects of interest into the fovea and keeps them there, but visual sensitivity has been shown to deteriorate while the eyes are moving. Here we show that human sensitivity for some visual stimuli is improved during smooth pursuit eye movements. Detection thresholds for briefly flashed, colored stimuli were 16% lower during pursuit than during fixation. Similarly, detection thresholds for luminance-defined stimuli of high spatial frequency were lowered. These findings suggest that the pursuit-induced sensitivity increase may have its neuronal origin in the parvocellular retino-thalamic system. This implies that the visual system not only uses feedback connections to improve processing for locations and objects being attended to, but that a whole processing subsystem can be boosted. During pursuit, facilitation of the parvocellular system may reduce motion blur for stationary objects and increase sensitivity to speed changes of the tracked object. [ABSTRACT FROM AUTHOR]

The pathways controlling motor behavior are believed to exhibit little selectivity for color, but there is growing evidence suggesting that color signals can be used to guide actions. We investigated this by having observers make a saccade or a rapid pointing movement to a small, peripherally flashed (100 ms) Gaussian target (SD=0.5°) defined exclusively by luminance (maximum contrast) or color (from cardinal DKL red–green or blue–yellow axes, at maximum saturation). We found no difference in saccadic or pointing accuracy for luminance or color targets. The same was true using shutter goggles during pointing (to minimize the use of external cues), and when the luminance contrast of color targets was varied by up to ±10%. In terms of response times, both eye and hand latencies increased with target eccentricity for R–G targets only, in a manner consistent with the sensitivity of this channel across eccentricity. We found little difference in response latencies between luminance and color targets once matched in terms of cone contrast. While RTs were longer when coupled with a goal directed pointing movement (versus a simple reaction without pointing), the difference was the same for color or luminance targets, suggesting that the spatial coding for the movements was also the same. In a final experiment we compared the accuracy of pointing to color-naming performance in a 4AFC procedure. The psychometric functions relating pointing accuracy (% correct quadrant) to color-naming (% correct color-name) were identical. Taken together, the results show that human observers can efficiently use pure chromatic signals to guide actions. [ABSTRACT FROM AUTHOR]