A new estimation of the duration of attentional dwell time

How rapidly can attention move from one object to the next? Previous studies in which the dwell time paradigm was used have estimated attentional switch times of 200–500 msec, results incompatible with the search rate estimates of 25–50 msec shown in numerous visual search studies. It has been argued that dwell times are so long in the dwell time paradigm because the attentional shifts measured are unlike those used in visual search. In the present experiment, a variation of a visual search task was used, in which serial endogenous (volitional) deployments of attention were measured directly by means of a probe reaction time task. The experiment revealed a dwell time of about 250 msec, consistent with the faster estimates from other dwell time studies. This result suggests that endogenous shifts of attention may be relatively slow and that the faster attentional shifts estimated from visual search tasks may be due to the involvement of bottom-up processes.     

Reaction times and electromechanical delay in reactions of increasing and decreasing force

The purpose of this study was to compare reaction times and electromechanical delay between reactions to increase force from rest and reactions to decrease force from an active state in the quadriceps femoris of healthy young adults. Force, position, and electromyographic data were recorded from 35 subjects reacting to a forced knee-flexion perturbation. Electromechanical delay was assessed through cross-correlation of the filtered EMG and force data. Reaction time to increase force (M= 159.9 msec., 95% CI= 149.9-169.9 msec.) was significantly longer than RT to decrease force (M= 124.4 msec., 95% CI= 118.7-130.1 msec.). This difference was partially caused by a difference in electromechanical delay (RT to increase force electromechanical delay was 63 msec., 95% CI=60-67 msec., greater than the RT to decrease force electromechanical delay of 49 msec., 95% CI=46-52 msec.). This difference in reaction time could be important in identifying and interpreting physiologically meaningful changes in muscle force and in intermuscular coordination during movement.     

Negative priming without reaction time: Effects on identification of masked letters

Responses to an object are often slower and/or less accurate if that object is related to a recently ignored object. Thisnegative priming effect has previously been examined only in reaction time tasks. In the present experiment, target letters and flanking distractor letters were displayed for 33, 100, or 300 msec, followed by a pattern mask. Subjects attempted to identify the target letters, with no demand for speed. Identification accuracy was reduced for targets that matched distractors presented on the immediately preceding trial. However, there was no bias against reporting preceding distractors on catch trials with no presented target. Implications for theories of negative priming are discussed.     

Effect of directional response variables on eye-hand reaction times and decision time

To determine if direction of response affects reaction time, we measured the time for hand response to a visual stimulus, using a sensitive, microprocessor-based testing device to determine simple reaction time (RT), choice RT, and decision time. Mean simple RT was 207 +/- 3.7 msec. (mean +/- SEM); mean choice RT was 268 +/- 4.2 msec; and mean decision time was 61 msec. No differences were noted for leftward versus rightward movements, or midline versus lateral movements. Choice RT increased by 1.49 msec./yr. of age. Simple RT increased significantly with age for the nondominant hand, but not for the dominant hand. Right-handed subjects were more rapid with the dominant hand for choice RT. We conclude that dominance of hand tested and test initiation mechanism have major effects, but direction of movement in the lateral plane has little effect on reaction time.     

Movement time and velocity as determinants of movement timing accuracy

Three experiments investigated the effect of movement time (MT) and movement velocity on the accuracy and initiation of linear timing movements. MTs of 100, 200, 500, 600, and 1000 msec were examined over various distances; timing accuracy decreased with longer MTs and slower average velocities. The velocity effect was independent of MT and occurred when the velocities were above and below about 15 cm/sec. Self-paced initiation times to movement increased directly with MT and inversely as a function of movement velocity. The latency data complement the MT findings in suggesting that average velocity is a key parameter in the initiation and control of discrete timing movements and, that there is some lower velocity below which movement control breaks down.     

The utilization of visual feedback information during rapid pointing movements

Three experiments were conducted to determine how variables other than movement time influence the speed of visual feedback utilization in a target-pointing task. In Experiment 1, subjects moved a stylus to a target 20 cm away with movement times of approximately 225 msec. Visual feedback was manipulated by leaving the room lights on over the whole course of the movement or extinguishing the lights upon movement initiation, while prior knowledge about feedback availability was manipulated by blocking or randomizing feedback. Subjects exhibited less radial error in the lights-on/blocked condition than in the other three conditions. In Experiment 2, when subjects were forced to use vision by a laterally displacing prism, it was found that they benefited from the presence of visual feedback regardless of feedback uncertainty even when moving very rapidly (e.g. less than 190 msec). In Experiment 3, subjects pointed with and without a prism over a wide variety of movement times. Subjects benefited from vision much earlier in the prism condition. Subjects seem able to use vision rapidly to modify aiming movements but may do so only when the visual information is predictably available and/or yields an error large enough to detect early enough to correct.     

Periodicity within reaction time distributions and electromyograms

This study investigates a periodic component in reaction time frequency distributions, that is, a tendency for responses to occur at regular, discrete intervals of time after stimulus presentation. Reaction time frequency distributions were plotted by a Computer of Average Transients and were obtained under stimulus conditions varying in sense modality stimulated (auditory and visual), and the intensity, colour, and duration of stimulation. The results indicated that there was periodicity in reaction time frequency distributions with a modal period of approximately 25 msec. It was found that the periodicty (a) was most evident when there was considerable variability in reaction time, and (b) tended to attenuate when a large number of reaction times were grouped. Other stimulus conditions appeared to have little effect on the periodicity. A significant correlation was found between the frequency of periodicity in the reaction time distributions and the electromyograms, both having a modal period of 25 msec. It was concluded that the periodicity in reaction time was the result of motor processes.     

Reaction time measurement of temporal integration and organization of form

Temporal integration of patterned stimuli was investigated by introducing an interstimulus interval (ISI) between brief exposures of two matrices of illuminated squares. These matrices were identical except for their spatial displacement, arranged such that they could be superimposed to yield either horizontal or vertical stripes. Choice reaction times to the composite stripe orientation were a progressively increasing function of ISI, suggesting some integration over an ISI range in excess of 224 msec. Similar functions were obtained with both regular and irregular order of ISI presentation. The results from an additional experiment employing an extraneous warning signal discounted the possibility that preparatory factors developing over the ISI were responsible for the obtained reaction time functions.     

Sequence of preparatory set for response movement

Electromyographic reaction times (EMG-RTs) of the right biceps brachii muscle were examined for two movement patterns, elbow flexion and forearm supination, in 8 healthy male subjects under simple and complex RT conditions with varied preparatory intervals (PIs): 0, 200, 400, 600, and 800 msec. In the simple RT condition, the subject was informed of the movement patterns to be performed prior to beginning the trials. In the complex RT condition the subject had to choose one of the two movement patterns at the time of the presentation of a warning signal. The results indicated that: (1) compared with the simple RT condition a delay of about 100 msec. in over-all mean EMG-RT was observed at PI = 0 msec. in the complex RT condition; (2) the difference of over-all mean EMG-RT between the two RT conditions disappeared when PI = 400 msec.; and (3) the difference in EMG-RTs between flexion and supination in the complex RT condition became the same as that in the simple RT condition when PI = 700 msec. It is assumed that the preparatory set for response movements is organized in an order, resulting in the differentiation of RT.     

Delayed search for a concealed imprinted object in the domestic chick

Five-day-old chicks were accustomed to follow an imprinted object (a small red ball with which they had been reared) that was moving slowly in a large arena, until it disappeared behind an opaque screen. In experiments, each chick was initially confined in a transparent cage, from where it could see and track the ball while it moved towards, and then beyond, one of two screens. The screens could be either identical or differ in colour and pattern. Either immediately after the disappearance of the ball, or with a certain delay, the chick was released and allowed to search for its imprinted object behind either screen. The results showed that chicks took into account the directional cue provided by the ball movement and its concealment, up to a delay period of about 180 s, independently of the perceptual characteristics of the two screens. If an opaque partition was positioned in front of the transparent cage immediately after the ball had disappeared, so that, throughout the delay, neither the goal-object nor the two screens were visible, chicks were still capable of remembering and choosing the correct screen, though over a much shorter period of about 60 s. The results suggest that, at least in this precocial bird species, very young chicks can maintain some form of representation of the location where a social partner was last seen, and are also capable of continuously updating this representation so as to take into account successive displacements of the goal-object. Received: 17 January 1998 / Accepted after revision: 29 March 1998     

Effects of electromyographic biofeedback on reaction time and movement time

The effects of electromyographic (EMG) biofeedback on reaction time (RT) and movement time (MT) were investigated utilizing 42 right-handed, male subjects from a university population. Subjects were randomly divided into three groups, a control group and two experimental groups. Both experimental groups were exposed to their EMG signals from their triceps brachii during the task, one experimental group received written information explaining the purpose of the EMG was to improve performance through biofeedback. Reaction times of the first block of 25 trials were significantly faster than those on the subsequent three blocks of trials for all groups. This provided evidence of learning. No other significant effects for reaction times were observed. Mean movement time for the EMG-only group was significantly slower than the means of either the Control group or EMG-Biofeedback group, with no difference between the latter two. The differences between experimental groups may have been related to alteration of strategy, anxiety, motivation.     

Behavioral definition of minimal reaction time in monkeys

Two monkeys (Macaca mulatta) were trained to press a key after onset of a tone and to release it after a 1-sec fixed foreperiod terminated by a light. The effects of imposing temporal contingencies on key release reaction times were determined by reinforcing only those releases whose latencies from the light fell within a “payoff band”, two time limits 50 msec apart located at some delay following the light. Over several days this delay was first gradually decreased, shortening the interval between light and payoff band, and then gradually increased again. For each delay, the median reaction time and a measure of variability were obtained from the latency distribution. For both animals, median latency could be decreased to 180 msec with the variability remaining small. Moving the payoff band still closer to the light resulted in further decrease in median latency but an abrupt increase in variability. This is in agreement with a model for simple reaction time derived from human research which suggests that this increased variability results from the inclusion of high-variability foreperiod time estimations in the latency distribution. These results indicate that interpretation of monkey response latencies as “minimal reaction times” requires examination of temporal reinforcement contingencies and variability of latencies.     

Attenuation of size illusion effect in dual-task conditions

We over-estimate or under-estimate the size of an object depending its background structure (e.g., the Ebbinghaus illusion). Since deciding and preparing to execute a movement is based on perception, motor performance deteriorates due to the faulty perception of information. Therefore, such cognitive process can be a source of a failure in motor performance, although we feel in control of our performance through conscious cognitive activities. If a movement execution process can avoid distraction by the illusion-deceived conscious process, the effect of the visual illusion on visuomotor performance can be eliminated or attenuated. This study investigated this hypothesis by examining two task performances developed for a target figure inducing the Ebbinghaus size illusion: showing visually perceived size of an object by index finger-thumb aperture (size-matching), and reaching out for the object and pretending to grasp it (pantomimed grasping). In these task performances, the size of the index finger-thumb aperture becomes larger or smaller than the actual size, in accordance with the illusion effect. This study examined whether the size illusion effect can be weakened or eliminated by the dual-task condition where actors’ attention to judge the object’s size and to produce the aperture size is interrupted. 16 participants performed the size-matching and pantomimed grasping tasks while simultaneously executing a choice reaction task (dual task) or without doing so (single task). Using an optical motion capture system, the size-illusion effect was analyzed in terms of the aperture size, which indicates the visually perceived object size. The illusion effect was attenuated in the dual task condition, compared to it in the single task condition. This suggests that the dual task condition modulated attention focus on the aperture movement and therefore the aperture movement was achieved with less distraction caused by illusory information.     

Adobe Flash as a medium for online experimentation: A test of reaction time measurement capabilities

Adobe Flash can be used to run complex psychological experiments over the Web. We examined the reliability of using Flash to measure reaction times (RTs) using a simple binary-choice task implemented both in Flash and in a Linux-based system known to record RTs with millisecond accuracy. Twenty-four participants were tested in the laboratory using both implementations; they also completed the Flash version on computers of their own choice outside the lab. RTs from the trials run on Flash outside the lab were approximately 20 msec slower than those from trials run on Flash in the lab, which in turn were approximately 10 msec slower than RTs from the trials run on the Linux-based system (baseline condition). RT SDs were similar in all conditions, suggesting that although Flash may overestimate RTs slightly, it does not appear to add significant noise to the data recorded.     

Absence of exposure time influence on lateralized face recognition and object naming latency tasks

J. Sergent (1982, Perception & Psychophysics, 31, 451-461; 1983, Psychological Bulletin, 93, 481-512) postulates that the left cerebral hemisphere preferentially extracts higher spatial frequency information, while the right hemisphere preferentially extracts lower frequency spatial information, from the visual scene. According to this view, shorter exposure times favor better right than left hemisphere performance, while longer exposure times favor better left than right hemisphere performance on tachistoscopic laterality tasks. We studied the effects of a threefold variation (40 msec versus 120 msec) in exposure duration, with constant 3-mL luminance, on face recognition and on object naming latency task performances. These are the same stimulus parameters employed by J. Sergent (1983, Psychological Bulletin, 93, 481-512) to demonstrate exposure duration effects in a task requiring the judgment of the sex of models from face photographs. We found the expected LVF superiority on the face recognition task and RVF superiority on the object naming task. There was, however, no influence of exposure duration on the performances. It is concluded that these tasks, which tap established lateralized processing asymmetries, are quite robust in their resistance to exposure time influence.     

The time course of configural change detection for novel 3-D objects

The present study investigated the time course of visual information processing that is responsible for successful object change detection involving the configuration and shape of 3-D novel object parts. Using a one-shot change detection task, we manipulated stimulus and interstimulus mask durations (40—500 msec). Experiments 1A and 1B showed no change detection advantage for configuration at very short (40-msec) stimulus durations, but the configural advantage did emerge with durations between 80 and 160 msec. In Experiment 2, we showed that, at shorter stimulus durations, the number of parts changing was the best predictor of change detection performance. Finally, in Experiment 3, with a stimulus duration of 160 msec, configuration change detection was found to be highly accurate for each of the mask durations tested, suggesting a fast processing speed for this kind of change information. However, switch and shape change detection reached peak levels of accuracy only when mask durations were increased to 160 and 320 msec, respectively. We conclude that, with very short stimulus exposures, successful object change detection depends primarily on quantitative measures of change. However, with longer stimulus exposures, the qualitative nature of the change becomes progressively more important, resulting in the well-known configural advantage for change detection.     

Erratum to: Chimpanzees (Pan troglodytes) accurately compare poured liquid quantities

Although many studies have shown that nonhuman animals can choose the larger of two discrete quantities of items, less emphasis has been given to discrimination of continuous quantity. These studies are necessary to discern the similarities and differences in discrimination performance as a function of the type of quantities that are compared. Chimpanzees made judgments between continuous quantities (liquids) in a series of three experiments. In the first experiment, chimpanzees first chose between two clear containers holding differing amounts of juice. Next, they watched as two liquid quantities were dispensed from opaque syringes held above opaque containers. In the second experiment, one liquid amount was presented by pouring it into an opaque container from an opaque syringe, whereas the other quantity was visible the entire time in a clear container. In the third experiment, the heights at which the opaque syringes were held above opaque containers differed for each set, so that sometimes sets with smaller amounts of juice were dropped from a greater height, providing a possible visual illusion as to the total amount. Chimpanzees succeeded in all tasks and showed many similarities in their continuous quantity estimation to how they performed previously in similar tasks with discrete quantities (for example, performance was constrained by the ratio between sets). Chimpanzees could compare visible sets to nonvisible sets, and they were not distracted by perceptual illusions created through various presentation styles that were not relevant to the actual amount of juice dispensed. This performance demonstrated a similarity in the quantitative discrimination skills of chimpanzees for continuous quantities that matches that previously shown for discrete quantities.     

The tunnel effect,Gibson's perception theory,and reflective seeing

Summary Subjects can have continuous visual experience of an object's movement across a display though the movement's middle phase takes place behind an opaque screen. The present article considers explanatory issues pertaining to this so-called, tunnel effect, with special reference to Gibson' s perception theory and the visual activity that I have been calling reflective seeing. Among the issues discussed are the following. (a) In the tunnel experiments, I suggest, there occur both persisting perception, as Michotte held, and persistence perception, as Gibson held. The subjects pick up stimulus information that allows visually experiencing the object's going out of sight at one edge of the screen and coming back into sight at another edge of the screen; the subjects have visual experience of the continued existence and movement of the object while it is out of sight. Moreover, persistence of perceptual experience is involved: when the object goes out of sight, the subjects' visual experience of its movement goes on. (b) I also argue that the tunnel effect is a phenomenon of both straightforward and reflective seeing. Adopting a phenomenal attitude, as one does when reporting one's perceptual experience, one still sees movement taking place on the other side of the screen, as one does in straightforward seeing. However, whereas straightforward seeing does not give inner awareness of visual experience, the subjects in the tunnel experiments report visually experiencing the object's movement while also visually experiencing the opaque screen in front of it as opaque. I argue that these reports, and those about the object's going out of and coming back into sight, must be based on the kind of visual experience that is part and product of reflective seeing.     

Determining subprocesses of visual feature search with reaction time models

After the classic serial/parallel dichotomy of visual search mechanisms has been increasingly doubted, we investigated what search mechanisms are used between the two poles termed "pop-out" and "strictly serial search" in an overt feature search paradigm. Since reaction time slopes do not contain sufficient information for this purpose, we developed a novel technique for analyzing reaction times. Individual reaction times are modeled as sums of the durations of successive search steps. Model parameters are task characteristics (similarity, number and arrangement of target and distractors) and processing characteristics of the participant (e.g., attention dwell and shift durations). In Experiment 1, several model variants were fitted numerically to empirical reaction times. The best fitting model suggested that more than one item can be processed in a single fixation, movement of attention is abrupt and not continuous, and even in pop out search, attention is often explicitly moved to the target. In Experiment 2, we measured the central model parameter, the so-called range of attention, more directly and thereby validated the model. The model provides an explanation for the strong variation in the slope of reaction time functions, which is not based on an explicit distinction between parallel and serial search processes.     

Object retrieval in the 1st year of life: learning effects of task exposure and box transparency

Before 12 months of age, infants have difficulties coordinating and sequencing their movements to retrieve an object concealed in a box. This study examined (a) whether young infants can discover effective retrieval solutions and consolidate movement coordination earlier if exposed regularly to such a task and (b) whether different environments, indexed by box transparency, would impact the rate of learning and time of discovery of these solutions. Infants (N=12) were presented with an object retrieval task every week from 6 1/2 months of age until they were able to retrieve the toy from the box using coordinated two-handed patterns for 3 weeks. To reach that criterion, infants tested with an opaque box took 2 1/2 months and infants tested with a semitransparent box took 1 1/2 months. Both groups outperformed age-matched controls who received a one-time exposure to the task. Repeated exposure to the task and vision of the toy significantly enhanced this process of solution discovery.