Visual working memory has been proven to be relatively robust against interference. However, little is known on whether such robust coding is obligatory, or can be flexibly recruited depending on its expected usefulness. To address this, participants remembered both the color and orientation of a grating. During the maintenance, we inserted a secondary color/orientation memory task, interfering with the primary task. Crucially, we varied the expectations of the type of interference by varying the probability of the two types of intervening task. Behavioral data indicate that to-be-remembered features for which interference is expected are bolstered, whereas to-be-remembered features for which no interference is expected are left vulnerable. This was further supported by fMRI data obtained from visual cortex. In conclusion, the flexibility of visual working memory allows it to strengthen memories for which it anticipates the highest risk of interference.

Different theories have been proposed to explain how the human brain derives an accurate sense of time. One specific class of theories, intrinsic clock theories, postulate that temporal information of a stimulus is represented much like other features such as color and location, bound together to form a coherent percept. Here, we explored to what extent this holds for temporal information after it has been perceived and is held in working memory for subsequent comparison. We recorded EEG of participants who were asked to time stimuli at lateral positions of the screen followed by comparison stimuli presented in the center. Using well-established markers of working memory maintenance, we investigated whether the usage of temporal information evoked neural signatures that were indicative of the location where the stimuli had been presented, both during maintenance and during comparison. Behavior and neural measures including the contralateral delay activity, lateralized alpha suppression, and decoding analyses through time all supported the same conclusion: The representation of location was strongly involved during perception of temporal information, but when temporal information was to be used for comparison, it no longer showed a relation to spatial information. These results support a model where the initial perception of a stimulus involves intrinsic computations, but that this information is subsequently translated to a stimulus-independent format to be used to further guide behavior.

Human time perception is malleable and subject to many biases. For example, it has repeatedly been shown that stimuli that are physically intense or that are unexpected seem to last longer. Two competing hypotheses have been proposed to account for such biases: One states that these temporal illusions are the result of increased levels of arousal that speeds up neural clock dynamics, whereas the alternative “magnitude coding” account states that the magnitude of sensory responses causally modulates perceived durations. Common experimental paradigms used to study temporal biases cannot dissociate between these accounts, as arousal and sensory magnitude covary and modulate each other. Here, we present two temporal discrimination experiments where two flashing stimuli demarcated the start and end of a to-be-timed interval. These stimuli could be either in the same or a different location, which led to different sensory responses because of neural repetition suppression. Crucially, changes and repetitions were fully predictable, which allowed us to explore effects of sensory response magnitude without changes in arousal or surprise. Intervals with changing markers were perceived as lasting longer than those with repeating markers. We measured EEG (Experiment 1) and pupil size (Experiment 2) and found that temporal perception was related to changes in ERPs (P2) and pupil constriction, both of which have been related to responses in the sensory cortex. Conversely, correlates of surprise and arousal (P3 amplitude and pupil dilation) were unaffected by stimulus repetitions and changes. These results demonstrate, for the first time, that sensory magnitude affects time perception even under constant levels of arousal.

Evidence shows that observers preactivate a target representation in preparation of a visual selection task. In this study, we addressed the question if and how preparing to ignore an anticipated distractor differs from preparing for an anticipated target. We measured EEG while participants memorized a laterally presented color, which was cued to be either a target or a distractor in two subsequent visual search tasks. Decoding the location of items in the search display from EOG channels revealed that, initially, the anticipated distractor attracted attention and could only be ignored later during the trial. This suggests that distractors could not be suppressed in advance but were represented in an active, attention-guiding format. Consistent with this, lateralized posterior alpha power did not dissociate between target and distractor templates during the delay periods, suggesting similar encoding and maintenance. However, distractor preparation did lead to relatively enhanced nonlateralized posterior alpha power, which appeared to gate sensory processing at search display onset to prevent attentional capture in general. Finally, anticipating distractors also led to enhanced midfrontal theta power during the delay period, a signal that was predictive of how strongly both target and distractor were represented in the search display. Together, our results speak against a distractor-specific advance inhibitory template, thus contrary to the preactivation of specific target templates. Rather, we demonstrate a general selection suppression mechanism, which serves to prevent initial involuntary capture by anticipated distracting input.

Current theories assume a functional role for covert attention in the maintenance of spatial information in working memory. Consistent with this view, both the locus of attention and positions stored in working memory can be decoded based on the topography of oscillatory alpha-band (8–12 Hz) activity on the scalp. Thus far, however, alpha modulation has been studied in isolation for covert attention and working memory tasks. Here, we applied an inverted spatial encoding model in combination with EEG to study the temporal dynamics of spatially specific alpha activity during a task that required observers to visually select a target location while maintaining another independently varying location in working memory. During the memory delay period, alpha-based spatial tuning functions shifted from the position stored in working memory to the covertly attended position and back again after the attention task was completed. The findings provide further evidence for a common oscillatory mechanism in both the selection and the maintenance of relevant spatial visual information and demonstrate the dynamic trade-off in prioritization between two spatial tasks.

Prominent theories of attention claim that visual search is guided through attentional templates stored in working memory. Recently, the contralateral delay activity (CDA), an electrophysiological index of working memory storage, has been found to rapidly decrease when participants repeatedly search for the same target, suggesting that, with learning, the template moves out of working memory. However, this has only been investigated with pop-out search for distinct targets, for which a strong attentional template may not be necessary. More effortful search tasks might rely more on an active attentional template in working memory, leading to a slower handoff to long-term memory and thus a slower decline of the CDA. Using ERPs, we compared the rate of learning of attentional templates in pop-out and effortful search tasks. In two experiments, the rate of decrease in the CDA was the same for both search tasks. Similar results were found for a second component indexing working memory effort, the late positive complex. However, the late positive complex was also sensitive to anticipated search difficulty, as was expressed in a greater amplitude before the harder search task. We conclude that the amount of working memory effort invested in maintaining an attentional template, but not the rate of learning, depends on search difficulty.

Visual search is facilitated if half the distractors are presented as a preview prior to the presentation of the target and second set of distractors-the preview benefit [Watson, D. G., & Humphreys, G. W. Visual marking: Prioritizing selection for new objects by top-down attentional inhibition of old objects. Psychological Review, 104, 90-122, 1997]. On one account, the preview advantage is due to automatic capture of attention by the onsets in the second, search display [Donk, M., & Theeuwes, J. Visual marking beside the mark: Prioritizing selection by abrupt onsets. Perception & Psychophysics, 93, 891-900, 2001]. We provide a neuropsychological test of this assertion. We examined onset capture and preview benefits in search in a group of neuropsychological patients with unilateral parietal damage. We demonstrate a normal pattern of performance when patients detected targets defined by onsets relative to those defined by offsets, irrespective of whether the onset target fell contra-or ipsilateral to the lesion. In contrast, there was a normal preview benefit in search only for ipsilesional targets, and preview search was impaired in the contralesional field. The data demonstrate that the preview benefit can dissociate from the onset advantage in search, and that onsets remain strongly weighted for attention even in the contralesional field of patients with parietal lesions.