On the time course of letter perception: A masked priming ERP investigation

In an experiment measuring event-related brain potentials (ERPs), single-letter targets were preceded by briefly presented masked letter primes. Name and case consistency were manipulated across primes and targets so that the prime was either the same letter as the target (or not), and was presented in the same case as the target (or not). Separate analyses were performed for letters whose upper- and lowercase forms had similar features (or not). The results revealed an effect of prime-target visual similarity between 120 and 180 msec, an effect of case-specific letter identity between 180 and 220 msec, and an effect of case-independent letter identity between 220 and 300 msec. We argue that these ERP results reflect processing in a hierarchical system for letter recognition that involves both case-specific and case-independent representations of alphabetic stimuli.     

Identification and pronunciation effects in a verbal reaction time task for words,pseudowords, and letters

The question addressed in this investigation was whether faster reading and pronunciation of words than orthographically regular pseudowords is due to faster identification or to faster programming and execution of the motor response. In Experiment I, three different response conditions (naming, threechoice signaled responding, and one-choice signaled responding) were employed to separate the identification and articulation processes in a verbal reaction time task. It was found that, for all intents and purposes, single, isolated letters are processed as if they were very short words. Words are read and pronounced 72 msec faster than pseudowords. Words are also pronounced 30 msec faster than pseudowords even if the reader has longer than 1 sec to identify the stimulus (three-choice condition) or to both identify the stimulus and preprogram the response (one-choice condition). The data indicate that words are identified about 52 msec faster and articulated about 30 msec faster than pseudowords. Since the number of response alternatives (one or three) does not interact with stimulus type (letter, word, or pseudoword) in the signaled response control condition, the 30-msec difference is due to response execution and not to differential response programming. Response programming takes in the neighborhood of 236 msec. Experiment 2 investigated the effect of local orthographic context upon the identification of the first letter of a string of letters. No difference was found in identifying the initial letter of words and pseudowords, but the initial letter of these orthographically regular letter strings was identified and named 10 msec faster than the initial letter of orthographically anomalous strings of letters (anagrams). The data from the two experiments are supportive of theories of reading that assume (1) that the letters of visually presented words are processed simultaneously, in parallel, (2) that there is a relatively direct access and retrieval of the phonological memory codes for the names of words, and (3) that orthographically regular pseudowords having no representation in the phonological lexicon undergo a grapheme-to-phoneme transformation that takes longer to finish than the direct spelling-to-sound process used for words.     

Temporal integration of vibrotactile patterns

Three experiments were conducted to measure the temporal integration of vibrotactile patterns presented to the fingertip. In Experiment 1, letters were divided in half and the time between the onsets of the first half of the letter and second half of the letter, stimulus onset asynchrony (SOA), was varied. The recognizability of the letters declined as the SOA was increased from 9 to 100 msec. In Experiment 2, the time between two patterns constituting a masking stimulus was varied and the stimulus effectiveness in interfering with letter recognition was determined. The amount of masking increased as the SOA increased from 9 to 50 msec. In Experiment 3, the SOA between a letter and its complement (the portions of the tactile array not activated by the letter) was varied. Increasing SOA from 9 to approximately 50 msec led to increasingly accurate letter recognition. The results of the three experiments suggest that the skin is capable of complete temporal integration over a time period of less than 10 msec, and that the temporal integration function becomes asymptotic in 50 to 100 msec. The results also suggest that the onset of a vibrotactile pattern is critical for generating contours. The implications of the results for modes of generating tactile patterns and for temporal masking functions are discussed.     

Visual search under conditions of very rapid sequential Input rates

The purposes of the present experiment were to provide information on rate of information processing in visual perception and to determine the degree to which the “sequential blanking” effect found by Mayzner. Tresselt, and Cohen (1966) constituted a limitation on rapid sequential input rates. A 10-channel tachisto scope was employed that permitted controlled durations of each of the 10 channels and the 9 inter channel intervals. The S’s task was one of visual search or detection in which he searched for a target letter among noise letters. A temporal interval forced-choice procedure was used. In addition to varying the rate at which letters were sequentially presented, various irregular temporal spatial orders of presentation of the letter sequences were employed and the direction and orientation of the display in the visual field was varied as was also the spacing between adjacent stimuli. No evidence of “sequential blanking” was found either in terms of the detection criterion or in the Ss’ phenomenal reports. Detection performance was as good at a rate of 2 1/2 msec per letter as it was at a rate of 30 msec per letter.     

Visual short-term memory for two sequential arrays: One integrated representation or two separate representations?

Two dot arrays, each containing a different set of six randomly selected locations from a 5 × 5 matrix, were presented briefly and were separated by an interstimulus interval (ISI) of 0, 200, 500, or 1,500 msec. Subjects were asked to remember these locations and to report whether a probe dot matched the locations in memory. To find out whether the subjects had formed an integrated representation of the two arrays, the probe dot was accompanied by matrix elements from the first array, from the second array, or from both arrays. Memory for Array 1 was significantly impaired when the retrieval context was drawn from Array 2, and vice versa, suggesting that the two arrays were represented separately. This effect was observed only at an ISI of 500 msec or longer. We propose that as Array 1 is better consolidated, its representation becomes more separated from that of Array 2.     

Retinal locus and the letter-span error function

The effect of retinal locus on the letter-span error function was investigated by requiring Ss to fixate at the left, middle, or right of lines of letters presented for 100 msec. Stimulus presentations consisted of lines of eight letters presented across the visual field, and lines of four letters presented alternately in the left and right visual hemifields. Locus of fixation and relative letter position were found to be significantly related to whether or not a letter was correctly localized. A significant interaction between locus of fixation and letter position was observed.     

The importance of being first: A tachistoscopic study of the contribution of each letter to the recognition of four-letter words

Three studies investigated the effect on the response time for voicing a four-letter word of delaying one of the letters or the entire word for intervals of up to 500 msec. Experiment I found delay of the first letter most detrimental, while delay of the second, third, or fourth letter facilitated performance. Experiment II confirmed these findings and indicated that delay of the entire word produced response times similar to delay of the first letter. Experiment III investigated the possibility that knowledge of the pronunciation of the first letter was the essential factor in facilitating performance when later letters were delayed. It was concluded that when pronunciation of the first letter was known, Ss were able to begin processing the word immediately.     

Capacity demands of automatic processes in semantic priming

Ben-Gurion University of the Negev, Beer Sheva, Israel In three experiments, we examined the effects of prime-target stimulus onset asynchrony (SOA) and the proportion of related primes and targets (relatedness proportion, or RP) on semantic priming when the prime was either named or was searched for a specific letter. In Experiment 1, with an RP of. 50, priming occurred at SOAs of 240 and 840 msec when the prime was named, but no priming was found at either SOA when the prime was searched for a letter. In Experiment 2 the RP was either. 20 or. 80, and the SOA was set at 1, 700 msec; priming again was found in both conditions when the prime was named, but only in the RP.80 condition when a letter search task was performed on the prime. In Experiment 3, both the proportion of related trials and SOA were varied; as in the previous experiments, no priming effects were found with the letter search task for either SOA in the RP.20 condition, but the priming effect was reinstated in the RP.80 condition. These results are discussed with respect to how limited capacity resources are allocated and how they influence semantic priming effects.     

Processing of tachistoscopic displays with controlled order of characters and spaces

The task used was designed to force Ss consistently to process the letters of a tachistoscopic display in the same spatial order, if Ss are able to process the letters in a brief display serially and if Ss have enough voluntary control over the selection of a processing order to use the order chosen by the E. In the main series of experiments the set of slides shown in each session included slides having a blank space in some position in the linear array of letters. For control, no-blank slides, a sharp, monotonic decrease in the percentage of correct detections of a signal letter with distance of the signal letter from the focusing dot was obtained. An unexpected result from the slides having a blank space was that detection of the signal letter was considerably more accurate on the slides having a blank space immediately following the signal letter than on the control slides having no blank space or the slides having a blank space immediately before the signal letter in the processing order. In one experiment blank spaces were replaced by black rectangles with no substantial change in the pattern of results. The results from the slides having a blank space or a black rectangle were interpreted as indicating that the onset of processing the image of a letter was determined by the distance in the display from the focusing dot to the letter and that the duration of processing an image of a letter was determined by the distance in the display from the letter to the next letter in the processing order.     

Evidence for an addition to the reading scan hypothesis

Letters were tachistoscopically presented in pairs to the left or right of fixation for 40 msec. The pair consisted of a target letter (B, D, P, or T) and a noise letter (all other letters of the alphabet except I), with the noise letter appearing either to the inside or the outside of the stimulus letter. S’s task was to report verbally the target letter as fast as possible. Reaction times and number of errors indicated that there was more interference when the noise letter occurred further from the fixation point than the target letter for both the left and right visual field. Since a reading scan cannot account for the results in the right visual field, an outside-toward-fixation scan is proposed. An analysis of the different kinds of errors indicated that the outside to fixation scan is more primitive than the reading scan in that it produces less detailed information about the letters than does the reading scan.     

Connectedness affects dot numerosity judgment: Implications for configural processing

Participants judged the number of dots in visual displays with brief presentations (200 msec), such that the numerosity judgment was based on an instantaneous impression without counting. In some displays, pairs of adjacent dots were connected by line segments, whereas, in others, line segments were freely hanging without touching the dots. In Experiments 1, 2A, and 2B, connecting pairs of dots by line segments led to underestimation of dot numbers in those patterns. In Experiment 3, we controlled for the number of freely hanging line segments, whereas Experiment 4 showed that line segments that were merely attached to dots without actually connecting them did not produce a considerable underestimation effect. Experiment 5 showed that a connectedness effect existed when stimulus duration was reduced (50 msec) or extended (1,000 msec). We conclude that connectivity affects dot numerosity judgments, consistent with earlier findings of a configural effect in numerosity processing. Implications of the role of connectedness in object representation are discussed.     

Combining letter-matching and tone discrimination: Evidence of automatic perceptual and spatial congruity effects

Dual task and priming paradigms were combined to investigate the distinction between automatic and attentional processes. Subjects in two experiments performed a primed letter-matching and a tone discrimination task separately and concurrently. The interval between prime onset and letter pair (SOA) was varied from 50 to 500 msec. Cost-benefit analyses in Experiment 1 indicated that primes that matched target letter pairs began to facilitate performance at an SOA of 150 msec. Primes inhibited performance when they mismatched identical letter pairs at SOA 100. In the dual-task situation, the benefits of priming letter targets were reflected in probe latencies with no evidence of concurrent costs in tone latencies. Experiment 2 revealed that two tasks could be primed simultaneously as effectively as when each was primed alone. Findings are discussed in reference to Posner and Snyder's (1975a, 1975b) two-process theory of priming and the applicability of a secondary task technique.     

Wholistic and analytic stimulus processing: The development of selective perceptual strategies

This experiment reports an investigation of the development of selective processing strategies as subjects become increasingly more practised at a serial self-paced RT task. It demonstrates the effect a preceding stimulus can have on the analysis of a current signal and the development of active analytic strategies in favour of passive wholistic processing, with practice. The stimuli used were letters with irrelevant visual noise dot patterns superimposed on them. The letter, or the dot pattern, or both, could be repeated on successive trials. Early in practice repetition of both stimulus components simultaneously produced short reponse latencies relative to repetition of the letter alone. The number of noise dots markedly affected RT. Late in practice, however, letter repetition RTs were small, irrespective of whether or not the noise dot pattern was repeated. Furthermore, the number of noise dots no longer had an effect on the RT to these stimulus transitions. The results suggest that subjects appear to be able to select relevant information to process as they become progressively more practised, even though there is evidence that they compare the current stimulus with an iconic representation of the immediately preceding one.     

Voluntary eyeblinks disrupt iconic memory

In the present research, we investigated whether eyeblinks interfere with cognitive processing. In Experiment 1, the participants performed a partial-report iconic memory task in which a letter array was presented for 106 msec, followed 50, 150, or 750 msec later by a tone that cued recall of onerow of the array. At a cue delay of 50 msec between array offset and cue onset, letter report accuracy was lower when the participants blinked following array presentation than under no-blink conditions; the participants made more mislocation errors under blink conditions. This result suggests that blinking interferes with the binding of object identity and object position in iconic memory. Experiment 2 demonstrated that interference due to blinks was not due merely to changes in light intensity. Experiments 3 and 4 demonstrated that other motor responses did not interfere with iconic memory. We propose a new phenomenon, cognitive blink suppression, in which blinking inhibits cognitive processing. This phenomenon may be due to neural interference. Blinks reduce activation in area V1, which may interfere with the representation of information in iconic memory.     

Interocular non-independence

Binocular interaction was studied by presenting a different letter form to each eye via a dichopic tachistoscope. The two dissimilar letters were presented simultaneously or at short delay internals of 0–200 msec and were either presented on corresponding or non-corresponding retinal areas. At delay internals of less than 100 msec stimulation of corresponding areas resulted in identification performance below that to be expected on the basis of independent chances to perceive. Stimulation on non-corresponding areas resulted in both presented letters being identified at the accuracy level predicted by an independence assumption.     

The effects of forced serial processing on identification of words and random letter strings

Skilled readers identified words and random letter strings displayed one letter at a time on the screen of a computer-controlled oscilloscope. Letters were either displayed in a single position, or painted left-to-right in adjacent positions. Adjacent displays were either unmasked, masked by a letter-like pattern following each letter (backward masking) or masked by a pattern preceding each letter (forward masking). Unmasked words were identified with a high degree of accuracy, and accuracy was independent of the exposure duration of the letters over the range 50–200 msec. Masked adjacent word displays and one-position word displays were identified much less accurately, and accuracy was highly dependent on letter exposure duration. In contrast to these results, identification of random strings, or of letters within random strings, was almost unaffected by the presence of the mask and was dependent on letter exposure duration under all display conditions. The results are interpreted as evidence that (a) masking forces subjects to process serial displays one letter at a time, and (b) words, or large segments of words, are habitually processed in parallel, while random strings are processed as a series of individual letters or small chunks.     

Naming and locating simultaneously and sequentially presented letters

Two letters varying in level of confusability were presented either simultaneously for 75 msec or sequentially for 75 msec each in adjacent retinal locations. The retinal locus of presentation varied from trial to trial, and subjects both identified and located the presented letters. Identification accuracy was higher on nonconfusable than on confusable letter pairs in the simultaneous condition, but not in the sequential condition. This result is interpreted as support for the notion that inhibition between similar or identical features shared by confusable letters occurs only when letters are presented simultaneously. A relative position effect, with performance on the peripheral letter higher than on the central letter, was found for simultaneously and second sequentially presented letters, but not for first sequentially presented letters. This result is interpreted in terms of the assumption that feature perturbations, with foveal perturbations more likely than peripheral perturbations, affect simultaneously and secondpresented letters, but not first-presented letters. The pattern of results for relative location accuracy showed many of the same effects as identification performance. A model assuming location errors reflect feature transpositions is outlined and is able to account for the absolute and relative location results and the correlation between relative location and identification accuracy.     

An analysis of the time course of attention in preview search

We used a probe dot procedure to examine the time course of attention in preview search (Watson & Humphreys, 1997). Participants searched for an outline red vertical bar among other new red horizontal bars and old green vertical bars, superimposed on a blue background grid. Following the reaction time response for search, the participants had to decide whether a probe dot had briefly been presented. Previews appeared for 1,000 msec and were immediately followed by search displays. In Experiment 1, we demonstrated a standard preview benefit relative to a conjunction search baseline. In Experiment 2, search was combined with the probe task. Probes were more difficult to detect when they were presented 1,200 msec, relative to 800 msec, after the preview, but at both intervals detection of probes at the locations of old distractors was harder than detection on new distractors or at neutral locations. Experiment 3A demonstrated that there was no difference in the detection of probes at old, neutral, and new locations when probe detection was the primary task and there was also no difference when all of the shapes appeared simultaneously in conjunction search (Experiment 3B). In a final experiment (Experiment 4), we demonstrated that detection on old items was facilitated (relative to neutral locations and probes at the locations of new distractors) when the probes appeared 200 msec after previews, whereas there was worse detection on old items when the probes followed 800 msec after previews. We discuss the results in terms of visual marking and attention capture processes in visual search.     

The effect of stimulus availability on task choice in voluntary task switching

The voluntary task switching paradigm allows subjects to choose which task to perform on each trial in a stimulus environment affording multiple tasks. The present study examined the effect of stimulus availability on task choice. Subjects viewed displays containing a digit and a letter and performed either an even/odd or a consonant/vowel judgment on each trial. The target stimuli appeared with a stimulus onset asynchrony (SOA) of 0, 50, 100, or 150 msec. The probability of performing the task associated with Stimulus 1 increased as SOA increased, indicating an effect of external or stimulus-driven factors on task choice. This effect of stimulus availability on task choice was greater when the response-stimulus interval was 400 msec than when it was 2,000 msec. This interaction of preparation interval and stimulus availability is explained within a model of task choice that includes both internal processes and external influences.     

Recognition vs recall of visually vs acoustically confusable letter matrices

In an attempt to separate auditory and visual components in short-term memory, five subjects were exposed to letter matrices composed of six visually confusable letters, six acoustically confusable letters, or a mixture of the two, under two response conditions: recognition and recall. A 50-msec stimulus presentation was followed by a variable dark interval of 1, 250, 1,000, or 3,000 msec. In the recall condition, the interval was followed by a buzzer which signaled the subject to recall, in any order, as many letters as possible. In the recognition condition, the variable interval was followed by a second letter matrix which was either identical to the first matrix or differed from is by one letter. Subjects responded either "same" or "different." The results support the notion that the auditory component plays a major role in recall, whereas the visual component dominates in recognition.