Past researchers of the integration of information in memory have typically required participants to attend to and/or commit to memory the stimuli conveying distinct features, rendering difficult the examination of whether the maintenance of the feature pairings can occur involuntarily. To address this issue, the integration of voice and location information in auditory sensory memory was measured using a cross-modal oddball task, in which task-irrelevant auditory deviants are known to capture attention in an involuntary fashion. Participants categorized visual digits presented shortly after to-be-ignored sounds. These sounds consisted in the same phoneme played simultaneously in both ears but in different voices (female in one ear, male in the other). On most trials, the pairing of voice to location was constant (standard sound). On rare and unpredictable trials, the voices swapped locations (deviant sound). In line with past work on attention capture by auditory novelty, the participants were significantly slower to judge the visual digits following the deviant sound, indicating the involuntary encoding of the links between voice and location in auditory memory. These results suggest that voices and locations are integrated in memory and that this binding occurs in conditions in which participants do not intend to commit any information to memory.

We present a computational model and corresponding computer simulations that mimic phenomenologically the eye movement trajectories observed in a conjunctive visual search task. The element of randomness is captured in the model through a Monte Carlo selection of a particular eye movement based on its probability, which depends on three factors, adjusted to match to the observed saccade amplitude distribution, forward bias in consecutive saccades, and return rates. Memory is assumed to operate through tagging of objects already recognized as nontargets, which, in turn, requires their processing within the attentional area of conspicuity (AC). That AC is adjusted so that computer simulations optimally reproduce the distribution of the number of saccades, the failure rate for capturing the target, and the return rate to previously inspected locations. For their viability, computer simulations critically depend on memory's being long-ranged. In turn, the simulations confirm the formation of circulating or spiraling patterns in the observed eye trajectories. We also relate consistently the average number of saccades per trial to the saccade amplitude distribution by modeling analytically the combined roles of the AC in attention and memory. The full Supplemental Appendix A for this article may be downloaded from <inter-ref>http://app.psychonomic-journals.org/content/supplemental</inter-ref>.

Executive working memory (WM) load reduces the efficiency of visual search, but the mechanisms by which this occurs are not fully known. In the present study, we assessed the effect of executive load on perceptual processing during search. Participants performed a serial oculomotor search task, looking for a circle target among gapped-circle distractors. The participants performed the task under high and low executive WM load, and the visual quality (Experiment 1) or discriminability of targets and distractors (Experiment 2) was manipulated across trials. By the logic of the additive factors method (Sternberg, <cross-ref>1969</cross-ref>, <cross-ref>1998</cross-ref>), if WM load compromises the quality of perceptual processing during visual search, manipulations of WM load and perceptual processing difficulty should produce nonadditive effects. Contrary to this prediction, the effects of WM load and perceptual difficulty were additive. The results imply that executive WM load does not degrade perceptual analysis during visual search.

The attentional blink (AB) refers to the finding that the perception of the second of two targets (T2) is impaired when presented in close temporal proximity to the first target (T1). An exception to this deficit occurs when T2 immediately follows T1, an effect referred to as lag 1 sparing. So far, it has been unclear whether the AB is location specific or nonspatial in nature. Most demonstrations of an AB across different locations have shown an absence of lag 1 sparing, due to accompanying spatial switch costs. This means that the AB pattern itself may be explained through such switch costs. In this study, to minimize spatial switch costs, attention was made to move continuously across multiple locations by aid of a cue. An AB across different locations was found, including lag 1 sparing. We conclude that the AB and lag 1 sparing are not tied to a location but represent a central deficit, in line with current theory.

In the present study, we explored the mechanisms involved in the contingent capture phenomenon, using a variant of the classic precuing paradigm of Folk, Remington, and Johnston (<cross-ref>1992</cross-ref>). Rather than keeping the target fixed over a whole block of trials (as has traditionally been done with contingent capture experiments), we encouraged participants to adopt a top-down set before each trial. If top-down attentional set determines which property captures attention, as is claimed by the contingent capture hypothesis, one would expect that only properties that match the top-down set would capture attention. We showed that even though participants knew what the target would be on the upcoming trial, both relevant and irrelevant properties captured attention (Experiment 1). An intertrial analysis (Experiments 1 and 2) showed that previous contingent capture findings may, to a large extent, be explained by intertrial priming. In addition, when participants were further forced into adopting the required top-down set (Experiments 3 and 4), irrelevant cues were suppressed, suggesting that top-down control might operate through disengagement of attention from the location of a property that does not match top-down goals. The present findings suggest that top-down control and intertrial priming make their own distinct contributions to the contingent capture phenomenon.

Although large variations in the magnitude of attentional capture have been evidenced across a wide range of studies and paradigms (see <cross-ref>Burnham, 2007</cross-ref>, for a review), the nature of these variations is unclear. In the present study, we used a modified spatial cuing task to address two related issues. In the first experiment, we explored the hypothesis that the magnitude of attentional capture varies systematically as a function of cue–target similarity. Targets of a particular color were preceded by uninformative peripheral cues carrying varying percentages of the target color. As was predicted, the magnitude of attentional capture varied directly with the similarity between cue and target. In the second experiment, we explored whether these similarity effects reflect a mixture of trials on which attention is fully captured and trials on which attention is not captured at all (i.e., a two-process model). A mixture analysis conducted on obtained reaction time distributions proved inconsistent with a two-process model.

In the present experiments, failures of selective visual attention were invoked using the B. A. Eriksen and C. W. Eriksen (<cross-ref>1974</cross-ref>) flanker task. On each trial, a three-letter stimulus array was flashed briefly, followed by a mask. The identity of the two flanking letters was response congruent, neutral, or incongruent with the identity of the middle target letter. On half of the trials, confidence ratings were obtained after each response. In the first three experiments, participants were highly overconfident in the accuracy of their responding to incongruent flanker stimulus arrays. In a final experiment, presenting a prestimulus target location cue greatly reduced both selective attention failure and overconfidence. The findings demonstrate that participants are often unaware of such selective attention failures and provide support for the notion that, in these cases, decisional processing is driven largely by the identities of the incongruent flankers. In addition, responding was invariably slower and sometimes more accurate when confidence was required than when it was not required, demonstrating that the need to provide posttrial confidence reports can affect decisional processing. Moreover, there was some evidence that the presence of neutral contextual flanking information can slow responding, suggesting that such nondiagnostic information can, indeed, contribute to decisional processing.