Time course of chord priming

The time course of chord priming was explored in four experiments. In chord priming, a chord (a typical combination of simultaneously sounded tones) primes other chords that are musically related. In the present study, the prime duration and the stimulus onset asynchrony (SOA) between the prime chord and the chord to be judged were varied. Priming occurred at an SOA and prime duration as short as 50 msec, the shortest tested. When the prime duration was held constant at 50 msec, priming occurred at an SOA as long as 2,500 msec, the longest tested, and the magnitude of the priming effect did not diminish. To eliminate a possible role of sensory memory in maintaining the priming effect during the silence following the prime, a 250-msec noise mask was presented immediately following the 50-msec prime. The interpolated noise mask did not eliminate priming, thereby supporting the view that chord priming is the consequence of associative activation.     

Time course of chord priming.

The time course of chord priming was explored in four experiments. In chord priming, a chord (a typical combination of simultaneously sounded tones) primes other chords that are musically related. In the present study, the prime duration and the stimulus onset asynchrony (SOA) between the prime chord and the chord to be judged were varied. Priming occurred at an SOA and prime duration as short as 50 msec, the shortest tested. When the prime duration was held constant at 50 msec, priming occurred at an SOA as long as 2,500 msec, the longest tested, and the magnitude of the priming effect did not diminish. To eliminate a possible role of sensory memory in maintaining the priming effect during the silence following the prime, a 250-msec noise mask was presented immediately following the 50-msec prime. The interpolated noise mask did not eliminate priming, thereby supporting the view that chord priming is the consequence of associative activation.     

Reflex inhibition in humans: Sensitivity to brief silent periods in white noise

A white noise (60 dB SPL) was always present except for brief silent periods (“gaps”) which occurred just before an eyelid reflex was elicited in human volunteers by a brief innocuous shock to the forehead. In Experiment 1 (n=8), 10-msec gaps (“S1”) were given 40, 80, 120, 160, or 200 msec before the shock (“S2”). Compared with S2-alone trials, the reflex was inhibited by about 50% at intervals of 80 msec and beyond. Experiment 2 (n=12) first provided detection thresholds for gaps using a simple version of the method of limits: on average a gap of 5.4 msec duration was just detected. Then gaps of 0, 2, 4, 6, 8, and 10 msec were given in random order, each 100 msec before S2. The 4-msec stimulus was an effective inhibitor of the reflex, and inhibition further increased on to 6- and then to 8-msec durations. A comparison of the values obtained on reflex inhibition with the 5.4-msec threshold obtained with the conventional psycho-physical test reveals that in humans reflex inhibition provides an objective index of stimulus detection that is at least of sufficient sensitivity to warrant its clinical application. The steady increase in reflex inhibition as gap duration increased from 2 to 8 msec may be of significance for tracing the rate of decay of afferent stimulation following noise offset, as it presumably reflects the growing sensitivity to the resumption of the noise as the duration of the silent period is increased.     

Semantic priming,prime reportability,and retroactive priming are interdependent

In two experiments, semantic analysis of prime words was measured in terms of facilitation in naming a semantically related target word. Targets were degraded but gradually clarified until the subject named them. Subjects reported the prime after naming the target. Experiment 1 used semantic associates as primes at a 50-msec prime-target stimulus onset asynchrony (SOA). Experiment 2 used both semantic-associate and identity primes at a 1,000-msec prime-target SOA. Reported primes showed facilitation in both experiments, whereas unreported primes did not. It appears that primes that undergo enough analysis to facilitate target processing are also available for conscious report. However, retroactive priming in both experiments showed that target processing also had an impact on prime reportability. The interdependence of priming and prime reportability disallows a straightforward interpretation of the origin of the facilitation.     

Automatic semantic feedback during visual word recognition

Four experiments were conducted to determine whether semantic feedback spreads to orthographic and/or phonological representations during visual word recognition and whether such feedback occurs automatically. Three types of prime-target word pairs were used within the mediated-priming paradigm: (1) homophonically mediated (e.g., frog-[toad]-towed), (2) orthographically mediated (e.g., frog-[toad]-told), and (3) associatively related (e.g., frog-toad). Using both brief (53 msec; Experiment 1) and long (413 msec; Experiment 3) prime exposure durations, significant facilitatory-priming effects were found in the response time data with orthographically, but not homophonically, mediated prime-target word pairs. When the prime exposure duration was shortened to 33 msec in Experiment 4, however, facilitatory priming was absent with both orthographically and homophonically mediated word pairs. In addition, with a brief (53-msec) prime exposure duration, direct-priming effects were found with associatively (e.g., frog-toad), orthographically (e.g., toad-told), and homophonically (e.g., toad-towed) related word pairs in Experiment 2. Taken together, these results indicate that following the initial activation of semantic representations, activation automatically feeds back to orthographic, but not phonological, representations during the early stages of word processing. These findings were discussed in the context of current accounts of visual word recognition.     

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.     

The effects of lead stimulus and reflex stimulus modality on modulation of the blink reflex at very short, short, and long lead intervals

The blink reflex is modulated if a weak lead stimulus precedes the blink-eliciting stimulus. In two experiments, we examined the effects of the sensory modality of the lead and blink-eliciting stimuli on blink modulation. Acoustic, visual, or tactile lead stimuli were followed by an acoustic (Experiment 1) or an electrotactile (Experiment 2) blink-eliciting stimulus at lead intervals of -30, 0, 30, 60, 120, 240, 360, and 4,500 msec. The inhibition of blink magnitude at the short (60- to 360-msec) lead intervals and the facilitation of blink magnitude at the long (4,500-msec) lead interval observed for each lead stimulus modality was relatively unaffected by the blink-eliciting stimulus modality. The facilitation of blink magnitude at the very short (-30- to 30-msec) lead intervals was dependent on the combination of the lead and the blink-eliciting stimulus modalities. Modality specific and nonspecific processes operate at different levels of perceptual processing.     

Semantic priming and identification of near threshold primes in a lexical decision task

Three experiments examined both the impact of semantic analysis of 50-msec, masked visual primes on a target response and the impact of semantic analysis of the target on a prime response. The first two experiments used a prime-target interval of 1000 msec. In Experiment 1, subjects reported the identity of each prime: (a) after a lexical decision about the target, (b) both before and after a lexical decision, or (c) after a target detection response. Prime report after both types of target response showed retroactive priming in which report was facilitated by related targets and inhibited by unrelated targets. Analyses of lexical decision latency and accuracy conditionalized on prime report showed that semantic priming was restricted to reported related primes. In Experiment 2, subjects made no overt response to the primes. Priming was conditionalized on recognition of the primes on a subsequent test. The pattern was the same as Experiment 1: There was priming only for recognized primes; recognition memory showed a pattern consistent with retroactive priming. Experiment 3 also conditionalized priming on recognition performance but used a prime-target interval of only 250 msec. Again, semantic priming was found only for recognized primes, and recognition memory revealed retroactive priming. Retroactive priming indicates an interdependency between prime and target processing that needs to be incorporated into models of semantic priming.     

Effects of Prime Type and Delay on Multiplication Priming: Evidence for a Dual-process Model

Two experiments investigated effects of numerical primes on production of simple multiplication facts (e.g. 4 × 8 = ?). In Experiment 1, a correct (32), related (24), unrelated (27), or neutral (##) prime appeared for 200 msec and was followed by a target problem at an ISI of 0, 750, or 1500 msec. Relative to neutral primes, correct primes produced constant RT and accuracy benefits across ISIs, and unrelated primes produced constant RT costs. Related primes produced costs compared to unrelated primes at the 0-msec ISI only. In Experiment 2, eliminating correct-answer primes from the stimulus set eliminated all the false-prime effects except the costs of related primes at the 0-msec ISI. We propose a dual-process account incorporating a familiarity-based name-the-prime strategy that produces benefits and costs insensitive to ISI and an automatic retrieval-priming process that is measurable only at short ISIs.     

The role of duration and rapid temporal processing on the lateral perception of consonants and vowels

This study explored the extent to which rapid temporal processing and duration contribute to the right-ear advantage (REA) and presumably left-hemisphere processing for stop consonants and the lack of clear-cut laterality effects for vowels. Three sets of synthetic stimuli were constructed: consonant vowel stimuli [ba da ga bi di gi bu du gu] of 300 msec duration (full stimuli) and two shortened stimuli consisting either of a noise burst and 40-msec transitions (40-msec stimuli), or a noise burst and 20-msec transitions (20-msec stimuli). Stimuli were presented dichotically for consonant, vowel, and syllable identification. Results indicated a significant REA for consonants in the full and 40-msec conditions and a non-significant REA in the 20-msec condition. Nevertheless, the magnitude of laterality did not change across the three conditions. These results suggest that although transition information including duration contributes to lateralization for stop consonants, it is the presence of abrupt onsets which crucially determines lateralized processing. For vowels, there was a significant REA only in the full stimulus condition, and a significant decrement in the magnitude of the laterality effect in the two shortened stimulus conditions. These results suggest that for vowel perception, it is the nature of the acoustic cue used for phonetic identification and not duration that seems to be the critical determinant of lateralization effects.     

Saccade latency and warning signals: Stimulus onset,offset, and change as warning events

Two experiments investigated saccade latency to a peripheral target under various warning signal conditions. In Experiment I, the effects of warning stimulus onset, change, and two offset conditions were compared at warning intervals of 0, 100, 300, and 600 msec. Warning stimulus onset, change, and offset were all effective in reducing saccade latency as compared to a no-warning control condition, but warning stimulus offset resulted in shorter saccade latency than onset or change at all warning intervals. Experiment 2 compared onset and offset warning conditions at ?300-, ?250-, ?200-, ?150-, ?100-, ?50-, 0-, and 50-msec intervals. Responses following onset were slower than those following offset at the latter five intervals, while warning onset resulted in slower saccades than no-warning control conditions at ?150-, ?100-, and ?50-msec intervals. These results indicate that the onset of a visual warning signal can have an interfering effect on the programming or execution of a saccade.     

Strategic reliance on phonological mediation in lexical access

The present study investigated strategic variation in reliance on phonological mediation in visual word recognition. In Experiment 1, semantically related or unrelated word primes preceded word, pseudohomophone (e.g.,trane), or nonpseudohomophone (e.g.,trank) targets in a lexical decision task. Semantic priming effects were found for words, and response latencies to pseudohomophones were longer in related than in unrelated prime conditions. In Experiment 2, related or unrelated word primes preceded word or pseudohomophone targets. A relatedness effect was found for words, although it was significant at a 600-msec prime-target stimulus onset asynchrony (SOA) and not at a 200-msec SOA. There was no relatedness effect for pseudohomophones. Experiment 3 was a replication of Experiment 2, except that pseudohomophones were replaced by nonpseudohomophonic orthographic controls. Facilitation effects for related target words were greater in Experiment 3 than in Experiment 2. The results reflect apparent variations in the expectation that a related prime reliably indicates that a target is a word. Although reliance on phonological mediation might be strategically contingent, there could be a brief time period in which phonologically mediated lexical access occurs automatically. Whether phonological information is maintained or suppressed subsequently depends on its overall usefulness for the task.     

Orientation invariance in visual object priming depends on prime—target asynchrony

Two experiments are reported in which orientation effects on visual object recognition latency were examined. In Experiment 1, we assessed picture-naming performance as a function of image-plane stimulus orientation and found increasing response times with increased misorientation of the stimulus. In Experiment 2, we examined the repetition priming effect on the identification of upright targets as a function of prime orientation. With time delays of 100, 200, or 500 msec between the onset of the prime and that of the target (i.e., stimulus onset asynchrony [SOA]), the magnitude of the priming effect decreased with increasing misorientation of the prime. These results contrast with the orientationinvariant priming effects reported in some previous repetition priming studies. These investigations all used relatively long prime—target SOAs. Confirming the crucial role of the latter variable, Experiment 2 shows that the magnitude of the repetition priming effect is invariant across prime orientations with an SOA of 1,000 msec. The possible implications of the present observations with respect to the issue of orientation invariance versus dependency of the visual object recognition process are discussed.     

Visual masking effects on duration,size, and form discrimination

In duration, size, and form discrimination tasks, a visual noise mask was presented at variable delays after stimulus offset in order to interrupt processing and control the extent of processing time. Previous work (Thomas & Cantor, 1975) had suggested that both perceived duration and perceived nontemporal “information” might be expected to increase as processing time was extended. As predicted, accuracy in the discrimination of size of circles and form of non-sense figures was found to vary directly with stimulus duration (20, 50 msec) and mask delay interval (0, 30, 70, 110 msec). Differences in perceived duration between filled (forms or circles) and unfilled (blank) intervals were found to increase monotonically with increases in the mask delay interval, when non-sense forms, but not circles, were presented. Two hypotheses of visual masking (“integration” and “interruption”) are discussed. Within the context of the “integration” hypothesis, a model is proposed which predicts processing time as a function of stimulus duration, mask delay interval, and the interval between onset of the mask and termination of processing.     

Orientation invariance in visual object priming depends on prime-target asynchrony

Two experiments are reported in which orientation effects on visual object recognition latency were examined. In Experiment 1, we assessed picture-naming performance as a function of image-plane stimulus orientation and found increasing response times with increased misorientation of the stimulus. In Experiment 2, we examined the repetition priming effect on the identification of upright targets as a function of prime orientation. With time delays of 100, 200, or 500 msec between the onset of the prime and that of the target (i.e., stimulus onset asynchrony [SOA]), the magnitude of the priming effect decreased with increasing misorientation of the prime. These results contrast with the orientation-invariant priming effects reported in some previous repetition priming studies. These investigations all used relatively long prime-target SOAs. Confirming the crucial role of the latter variable, Experiment 2 shows that the magnitude of the repetition priming effect is invariant across prime orientations with an SOA of 1,000 msec. The possible implications of the present observations with respect to the issue of orientation invariance versus dependency of the visual object recognition processare discussed.     

Developmental aspects of dichoptic viewing

Age-related performance changes on a dichoptic viewing task were examined with twenty-five (25) individuals in a cross-sectional design. Using a double-report procedure, subjects were asked to identify two different consonant-vowel graphemes presented separately to the same foveal area of each eye (i.e., dichoptic stimulation). Stimuli were presented at stimulus-onset asynchronies (SOAs) ranging from 0 to 300 msec in 50-msec steps. Results indicated that the number of both-correct trials (i.e., correct reports of both stimuli in a dichoptic pair) significantly increased with age, while single-correct trials (a correct report of only one stimulus in the pair) significantly decreased with age. In addition, the shape of the masking functions indicated lagging stimuli were reported more accurately than leading stimuli at SOAs of 50–300 msec for all subjects. Younger subjects exhibited peak masking effects for synchronous presentations (0-msec SOA) while older individuals showed peak masking at SOAs of 50 msec. Results suggest developmental performance changes noted in processing visual information parallel, to a remarkable degree, those observed in processing auditory information.     

Associative priming in color naming: interference and facilitation

In Experiment 1, color-naming interference for target stimuli following associated primes was greater in a group making a lexical decision to the prime than in a group reading the prime silently. High-frequency targets were responded to more quickly than low-frequency targets. In Experiment 2, with subjects naming the prime, there was evidence of associative interference when the prime and the target were grouped temporally but not when the intertrial interval was comparable with the prime-target interval. Associative primes presented at a short (120-msec) prime-target stimulus onset asynchrony facilitated color naming in Experiment 3. Taken together, the results suggest that the effect of faster processing of the base word in a color-naming task is facilitatory and that color-naming priming interference arises when associative prime processing increases conflict between word and color responses by enhancing phonological or articulatory activation of the base word.     

The facilitation of lexical decisions by a prime occurring after the target

Three experiments are reported that investigate priming effects in a lexical decision task. when the prime was presented after the target. In Experiment 1, the lexical decision target was presented for 50 msec, followed 80 msec later by the prime. No significant facilitation of responses was observed in the related prime condition. In Experiment 2, the target was presented for 30 msec, followed 35 msec later by the prime. Targets followed by related primes were responded to significantly faster than targets with unrelated primes. Experiment 3 replicated the result of Experiment 2. The data are interpreted as supporting parallel processing of the prime and target in semantic priming experiments. The theoretical implications of the “backward” priming effect are discussed.     

The time course of phonological, semantic, and orthographic coding in reading: Evidence from the fast-priming technique

The present experiment employed the fast-priming paradigm in reading (Sereno & Rayner, 1992), in which sentences are silently read while eye-movement-contingent changes are made on a specified target region. In this paradigm, when readers fixate on a specified target word region, a prime word is encountered for a brief duration at the beginning of the fixation and then it is replaced by a target word. Three types of primes were employed:homophones, semantically related, andorthographically similar, and five prime durations were employed: 29, 32, 35, 38, and 41 msec. The primary finding was that significant homophone priming was obtained at prime durations ranging from 29 to 35 msec, whereas significant semantic priming occurred only at the 32-msec prime duration. In contrast, significant orthographic priming occurred at all prime durations. These findings indicate that phonological codes are activated during an eye fixation at least as rapidly as semantic codes. An explanation for the pattern of events is suggested using the framework of an activation-verification model.     

Postsaccadic processing of the retinal image during picture scanning

Eye movements were monitored while observers inspected photographs of natural scenes. At the end of each saccade (i.e., at the beginning of each period of steady fixation), the stimulus was replaced for a certain period of time by a uniform field (Experiment 1) or a blurred version of the stimulus scene (Experiment 2). Total fixation duration was measured as a function of the duration of the initial uniform field or the blurred image that followed the saccade. It was found that fixation duration increased proportionally with the duration of the initial replacement field, even for durations as short as 25 msec. These results suggest that the visual system uses information on the retina right after each saccade is completed and that the blurred, low-resolution information used in Experiment 2 (cutoff frequency of 0.8 cpd) is not sufficient for the requirements of picture processing in this task.