Benefits from attention depend on the target type in location-precued discrimination.

In previous research, we found that precuing of attention to a target location greatly improved discrimination of targets that differed in line arrangement, but had little effect on discrimination of targets that differed in line orientation. In the present research, a number of other targets that represent various feature differences were used. The new data are consistent with and extend our earlier findings by showing that (1) there is some effect of precuing with all targets tested, and (2) the size of precuing effects varies in a complex way with the nature of the target. Moreover, the difficulty of the discrimination cannot explain the size of the precuing effects. A framework for understanding the events occurring during trials in the location-cuing paradigm is presented and applied to these results.     

Selectively ignoring locations does not modulate contingent involuntary orienting,but selectively attending does

Attending to a location in the visual field facilitates processing of objects in that location, and numerous studies have revealed processing benefits by precuing target locations. Recent studies have also demonstrated that precuing a location to ignore reduces distraction by items in that location; however, precuing a feature (colour) to ignore increases distractor interference, at least before a template for rejection is established. Thus, locations, not features, can be selectively ignored. The present study used a spatial cuing task to examine whether featurally-relevant items are selected when they appear in ignored locations. The results revealed contingent attentional capture by target-relevant cues (red cue when searching for red targets, but not for onset targets), even when the cue appeared in a location that was ignored. Importantly, this was equivalent to contingent capture elicited by cues in non-ignored locations. However, when observers were precued to the target location, contingent capture was largely eliminated. The results suggest salient items with target-relevant features are selected from selectively ignored locations, but focusing attention onto a location can preclude capture by salient and target-relevant items.     

Perceptual processing of nontargets in an attention task

The capability of nontargets to qualitatively influence the semantic processing of coincident targets was investigated in three experiments. Subjects were aurally presented a series of word pairs and attempted to detect homonymic instances of a predesignated category (e.g., animals). The nontarget with which a target (e.g., ANT) was paired was appropriate (e.g., CRAWLING), inappropriate (e.g., UNCLE), or neutral (e.g., STRAW). Experiments 1 and 2 established that detection of targets can be facilitated by appropriate nontargets and inhibited by inappropriate ones. Thus, nontargets can influence the way in which targets are semantically represented. Experiment 3 showed that this effect is eliminated when subjects are precued as to the ear of entry of targets. Thus, precuing appears to curtail the perceptual processing of nontargets. The data run counter to theories that claim that focused attention does not entail the perceptual suppression of nontargets.     

Manual asymmetries in the preparation and control of goal-directed movements

The primary purpose of this experiment was to determine if left hand reaction time advantages in manual aiming result from a right hemisphere attentional advantage or an early right hemisphere role in movement preparation. Right-handed participants were required to either make rapid goal-directed movements to small targets or simply lift their hand upon target illumination. The amount of advance information about the target for a particular trial was manipulated by precuing a subset of potential targets prior to the reaction time interval. When participants were required to make aiming movements to targets in left space, the left hand enjoyed a reaction advantage that was not present for aiming in right space or simple finger lifts. This advantage was independent of the amount or type of advance information provided by the precue. This finding supports the movement planning hypothesis. With respect to movement execution, participants completed their aiming movements more quickly when aiming with their right hand, particularly in right space. This right hand advantage in right space was due to the time required to decelerate the movement and to make feedback-based adjustments late in the movement trajectory.     

Endogenous visuospatial precuing effects as a function of age and task demands

This experiment examined the effects of age on processing resource capacity using an endogenous visuospatial precuing task and four levels of resource demands. Younger and older adults made speeded two-choice responses to dim and bright targets that required a line-orientation or a lexical decision. An arrow preceding target onset served as an attentional cue to affect the spatial distribution of resources. It provided accurate information about the target’s location on most trials and inaccurate or neutral information on the remaining trials. Although older adults were slower than younger adults under all conditions and were more affected by the resource demand manipulations, they exhibited a pattern of precuing effects across conditions that was similar to that of the younger adults. Results are consistent with the idea that the visuospatial attention system remains relatively unaffected by aging. However, the data speak against the idea that capacity reduction is the primary contributor to age-related slowing.     

Allocation of attention in texture segregation, visual search, and location-precuing paradigms

Is there a common mechanism (or set of mechanisms) that controls the allocation of spatial attention in texture segregation, visual search, and location-precuing tasks? This question was addressed by comparing data from our previous research on location-cuing and search tasks with data from a new set of experiments on texture segregation, in which a common set of stimuli was used across the three paradigms. However, when we ranked the scores for the targets on texture segregation speed, search rate, and improvement due to precuing effects, agreement between these measures was less than perfect. Further analyses of these results led to the following conclusions: (a) speed of texture segregation is affected by perceptual aspects of the display other than the attentional salience of a particular target; (b) visual search rate and the size of precuing effects are strongly related over most of the set of targets we used; and (c) some cases in which search rate was not consistent with size of precue effects may be related to the presence of nearby distractors in the search task.     

Mechanisms for precuing superiority in visual recognition

Superior recognition, when similar alternatives are studied prior to brief target pictures of common objects, is usually attributed to selective feature analysis, which is beneficial only when the target is not readily discriminable in the alternatives. The present study found equal precuing superiority, however, for similar and dissimilar alternatives with abstract geometric stimuli, and with pictures of common objects, precuing superiority occurred only when each alternative represented the same semantic category. Precuing effects did not appear when different categories were represented in the alternatives, and performance was similar to other conditions in which only a categorical match between target and alternatives was possible. These results suggest that selective feature analysis and precuing superiority only occur when the target cannot be identified by its semantic category. With dissimilar alternatives activation of the target's category can be used to select a response, and there is no benefit from precuing.     

Effects of viewing time,fixations, and viewing strategies on visual memory for briefly presented natural objects

We investigated the impact of viewing time and fixations on visual memory for briefly presented natural objects. Participants saw a display of eight natural objects arranged in a circle and used a partial report procedure to assign one object to the position it previously occupied during stimulus presentation. At the longest viewing time of 7,000 ms or 10 fixations, memory performance was significantly higher than at the shorter times. This increase was accompanied by a primacy effect, suggesting a contribution of another memory component—for example, visual long-term memory (VLTM). We found a very limited beneficial effect of fixations on objects; fixated objects were only remembered better at the shortest viewing times. Our results revealed an intriguing difference between the use of a blocked versus an interleaved experimental design. When trial length was predictable, in the blocked design, target fixation durations increased with longer viewing times. When trial length was unpredictable, fixation durations stayed the same for all viewing lengths. Memory performance was not affected by this design manipulation, thus also supporting the idea that the number and duration of fixations are not closely coupled to memory performance.     

Proactive inhibitory control of emotional distractors: Evidence for the benefit of precuing emotional distractors

The present study investigated the role of proactive inhibitory control in processing emotional distractors by examining the benefit of precuing the following emotional distractor. In Experiments 1A and 1B, an emotional flanker task was used while schematic emotional faces were presented as targets and distractors. We found the benefit of precuing the emotional distractor. In Experiment 2, the precue could not predict the following emotional distractor. The benefit of precuing the emotional distractor diminished, suggesting that the benefit was not due to reactive inhibition of the precued distractor. In Experiments 3A and 3B, an emotional Stroop task was used while schematic emotional faces were presented as distractors. The benefit of precuing the emotional distractors was observed when these distractors were emotional faces but not observed when the distractors were scrambled faces. These findings suggested that the benefit of precuing the emotional distractors operates at the emotional level.     

RSVP in orbit: Identification of single and dual targets in motion

Three experiments using rapid serial visual presentation (RSVP) tested participants' ability to detect targets in streams that are in motion. These experiments compared the ability to identify moving versus stationary RSVP targets and examined the attentional blink with pairs of targets that were moving or stationary. One condition presented RSVP streams in the center of the screen; a second condition used an RSVP that was orbiting in a circle, with participants instructed to follow the stream with their eyes; and a third condition had participants fixate in the middle while observing a circling RSVP stream. Relative to performance in stationary RSVP streams, participants were not markedly impaired in detecting single targets in RSVP streams that were moving, either with or without instructions to pursue the motion. In streams with two targets, a normal attentional blink effect was observed when participants were instructed to pursue the moving stream. When participants had to maintain central fixation as the RSVP stream moved, the attentional blink was nearly absent even when a trailing mask was added. We suggest that the reduction of the attentional blink for moving RSVP streams may reflect a reduced ability to perceive the temporal boundaries of the individual items.     

Programming tool-use actions

When humans plan to execute a tool-use action, they can only specify the bodily movement parameters by taking into account the external target or goal of the tool-use action and the target-movement mapping implemented by the tool. In this study, the authors used the movement precuing method to investigate how people prepare for actions made with tools. More specifically, they asked whether people would be able to specify the spatial target and the target-movement mapping of the tool-use action independently of each other, and to what degree they would be able to prepare these components in advance. In 3 experiments, they precued either the target or the target-movement mapping of tool-use actions involving either a compatible or an incompatible target-movement mapping. Results indicate that participants benefit from partial advance information about the target-movement mapping, whereas no significant effects were found for precuing the spatial target of the action. These results occurred regardless of whether the target-movement mapping was compatible or incompatible and provide evidence for the notion that the target-movement mapping of a tool-use action is part of its cognitive representation.     

The relationship between online visual representation of a scene and long-term scene memory

In 3 experiments the author investigated the relationship between the online visual representation of natural scenes and long-term visual memory. In a change detection task, a target object either changed or remained the same from an initial image of a natural scene to a test image. Two types of changes were possible: rotation in depth, or replacement by another object from the same basic-level category. Change detection during online scene viewing was compared with change detection after delay of 1 trial (Experiments 2A and 2B) until the end of the study session (Experiment 1) or 24 hr (Experiment 3). There was little or no decline in change detection performance from online viewing to a delay of 1 trial or delay until the end of the session, and change detection remained well above chance after 24 hr. These results demonstrate that long-term memory for visual detail in a scene is robust.     

Saccadic suppression relies on luminance information

To determine whether saccadic suppression of image displacement uses information from luminance channels, we measured spatial displacement detection thresholds with equiluminant and nonequiluminant targets during saccades. We compared these saccadic thresholds with displacement thresholds measured during fixation by making ratios of saccadic thresholds to fixation thresholds. Ratios were lower in the equiluminant condition than in the nonequiluminant. This surprising result indicates that detection of equiluminant target displacements during saccades was better than detection of nonequiluminant targets, compared with the detection abilities during fixation. Thus, saccadic suppression of image displacement, which should increase displacement thresholds during saccades over fixation thresholds, was more effective with nonequiluminant targets. Because of target flicker, displacement thresholds were anisotropic in the nonequiluminant condition; thresholds were greater when target and eye moved in the same direction than when they moved in opposite directions, consistent with earlier results. These two effects (flicker-induced anisotropy and greater suppression in nonequiluminance) canceled when the eye moved opposite the displacement, yielding equal thresholds, and summed when eye and target moved in the same direction, yielding large threshold differences. We conclude that saccadic suppression of image displacement uses mechanisms sensitive to luminance contrast.     

Vector averaging of inhibition of return

Observers detected targets presented 400 msec after a display containing one cue or two to four cues displayed simultaneously in randomly selected locations on a virtual circle around fixation. The cue arrangement was completely uninformative about the upcoming target’s location, and eye position was monitored to ensure that the participants maintained fixation between the cue and their manual detection response. Reflecting inhibition of return (IOR), there was a gradient of performance following single cues, with reaction time decreasing monotonically as the target’s angular distance from the cued direction increased. An equivalent gradient of IOR was found following multiple cues whose center of gravity fell outside the parafoveal region and, thus, whose net vector would activate an orienting response. Moreover, on these trials, whether or not the targeted location had been stimulated by a cue had little effect on this gradient. Finally, when the array of cues was balanced so that its center of gravity was at fixation, there was no IOR. These findings, which suggest that IOR is an aftermath of orienting elicited by the cue, are compatible with population coding of the entire cue (as a grouped array for multiple cues) as the generator of IOR.     

Prior entry explains order reversals in the attentional blink

When two targets are presented in rapid succession, the first target (T1) is usually identified, but the second target (T2) is often missed. A remarkable exception to this "attentional blink" occurs when T2 immediately follows the first T1, at lag 1. It is then often spared but reported in the wrong order--that is, before T1. These order reversals have led to the hypothesis that "lag 1 sparing" occurs because the two targets merge into a single episodic representation. Here, we report evidence consistent with an alternative theory: T2 receives more attention than T1, leading to prior entry into working memory. Two experiments showed that the more T2 performance exceeded that for T1, the more order reversals were made. Furthermore, precuing T1 led to a shift in performance benefits from T2 to T1 and to an equivalent reduction in order reversals. We conclude that it is not necessary to assume episodic integration to explain lag 1 sparing or the accompanying order reversals.     

Direction-specific motion thresholds for abnormal image shifts during saccadic eye movement

Eye movements were monitored and a target circle subtending an angle of 7^o was made to move during and dependent on the eye movements. Thresholds of detection of the resulting abnormal image displacements were obtained. Thresholds were low when both the eyes and the target moved either horizontally or vertically. They were higher by a factor of two or more when the eye movements and the target motions were not in the same plane. In the latter conditions, two processes account for the detection of target motion. One is a compensation process where the extent of that component of the motion of the retinal image of the target which is parallel to the eye movement is compared with the extent of the eye movement. The other process detects an angle between the plane of the target image motion and the plane of the eye movement. Our results indicate that the higher thresholds occurred when detection of this angle was required.     

Involuntary capture of visual-spatial attention occurs for intersections,both real and “imagined”

In three spatial precuing experiments, we demonstrate attentional capture by an intersection that occurs (1) between two lines that are not part of an enclosed object, and (2) between a line in the cuing array that is not physically present during target search and the invisible circumference of a perceptual circle formed by the elements in the target array. This capture effect conceptually replicates Cole, Gellatly, and Blurton’s (2001)corner enhancement effect, in which responses are faster for targets presented near an object’s corners rather than along its straight edges. However, it extends that effect by showing that it occurs even when the intersection is not part of an enclosed object and is not physically present during target search. More important, our capture effect occurred even though the target’s position was not designated by a perceptually distinctive feature and was not predicted by the intersection’s position. Thus, it seems that a line intersection—whether it be real or imaginary—automatically captures visual—spatial attention, contrary to Folk, Remington, and Johnston’s (1992) and Gibson and Kelsey’s (1998) views that such an involuntary capture of spatial attention is contingent on attentional control settings.     

Coordination dynamics and attentional costs of continuous and discontinuous bimanual circle drawing movements

It has been suggested that the temporal control of rhythmic unimanual movements is different between tasks requiring continuous (e.g., circle drawing) and discontinuous movements (e.g., finger tapping). Specifically, for continuous movements temporal regularities are an emergent property, whereas for tasks that involve discontinuities timing is an explicit part of the action goal. The present experiment further investigated the control of continuous and discontinuous movements by comparing the coordination dynamics and attentional demands of bimanual continuous circle drawing with bimanual intermittent circle drawing. The intermittent task required participants to insert a 400ms pause between each cycle while circling. Using dual-task methodology, 15 right-handed participants performed the two circle drawing tasks, while vocally responding to randomly presented auditory probes. The circle drawing tasks were performed in symmetrical and asymmetrical coordination modes and at movement frequencies of 1Hz and 1.7Hz. Intermittent circle drawing exhibited superior spatial and temporal accuracy and stability than continuous circle drawing supporting the hypothesis that the two tasks have different underlying control processes. In terms of attentional cost, probe RT was significantly slower during the intermittent circle drawing task than the continuous circle drawing task across both coordination modes and movement frequencies. Of interest was the finding that in the intermittent circling task reaction time (RT) to probes presented during the pause between cycles did not differ from the RT to probes occurring during the circling movement. The differences in attentional demands between the intermittent and continuous circle drawing tasks may reflect the operation of explicit event timing and implicit emergent timing processes, respectively.     

Gaze direction and the extraction of egocentric distance

The angular declination of a target with respect to eye level is known to be an important cue to egocentric distance when objects are viewed or can be assumed to be resting on the ground. When targets are fixated, angular declination and the direction of the gaze with respect to eye level have the same objective value. However, any situation that limits the time available to shift gaze could leave to-be-localized objects outside the fovea, and, in these cases, the objective values would differ. Nevertheless, angular declination and gaze declination are often conflated, and the role for retinal eccentricity in egocentric distance judgments is unknown. We report two experiments demonstrating that gaze declination is sufficient to support judgments of distance, even when extraretinal signals are all that are provided by the stimulus and task environment. Additional experiments showed no accuracy costs for extrafoveally viewed targets and no systematic impact of foveal or peripheral biases, although a drop in precision was observed for the most retinally eccentric targets. The results demonstrate the remarkable utility of target direction, relative to eye level, for judging distance (signaled by angular declination and/or gaze declination) and are consonant with the idea that detection of the target is sufficient to capitalize on the angular declination of floor-level targets (regardless of the direction of gaze).     

Is rapid performance improvement across short precue-target delays due to masking from peripheral precues?

The role of lateral masking in more rapid performance improvement with peripheral than with central precuing was investigated. A peripheral precue to the inside of the target location provided less masking at zero precue-target delay than a precue to the outside (experiment 1) or a precue involving a partial target at the target location (experiment 2). There was no significant interaction between precue-target delay and precue type in a comparison of inside precues and precues involving a briefly-brightened box around the target location, although overall performance was significantly poorer with the latter (experiment 3). Performance was better at short precue-target delays with inside precues than with central precues (experiment 4), yet it did not improve significantly more rapidly. Minimizing lateral masking with peripheral precues thus eliminates the dramatic performance improvement sometimes observed across short precue-target delays, causing performance to be consistently better than with central precues across these delays.