Conceptual activation of distractors during selection is not sufficient to produce negative priming

Negative priming (NP) occurs when responses are slower because the targets were distractors on the preceding trial. Word-naming NP occurs only with words that have been presented repeatedly as targets; novel words do not show NP. The activation-inhibition explanation is that representations of repeated-word distractors are activated already and must be inhibited; the inhibition carries over to the next trial. If this explanation is correct, novel-word NP should occur if the word is semantically primed (thus activating its representation) before it occurs as a distractor. In two experiments, there was NP for words from a repeated set, and the magnitude of NP increased when the same word could occur as a target on consecutive trials. There was positive, rather than negative, priming for novel-word targets that had been semantically primed as distractors. Either the activation from semantic priming was not sufficiently strong to require inhibition, or the activation-inhibition hypothesis does not refer to activation of conceptual representations.     

Parafoveal semantic processing of emotional visual scenes

The authors investigated whether emotional pictorial stimuli are especially likely to be processed in parafoveal vision. Pairs of emotional and neutral visual scenes were presented parafoveally (2.1 degrees or 2.5 degrees of visual angle from a central fixation point) for 150-3,000 ms, followed by an immediate recognition test (500-ms delay). Results indicated that (a) the first fixation was more likely to be placed onto the emotional than the neutral scene; (b) recognition sensitivity (A') was generally higher for the emotional than for the neutral scene when the scenes were paired, but there were no differences when presented individually; and (c) the superior sensitivity for emotional scenes survived changes in size, color, and spatial orientation, but not in meaning. The data suggest that semantic analysis of emotional scenes can begin in parafoveal vision in advance of foveal fixation.     

Mapping is not sufficient for specifying position in visual space

The general view is that one knows where an object is located in visual space on the basis of which neurons it activates. But there is reason to believe that a radically different method of specifying position is needed, one which identifies the position using coordinates. Those who study motor systems assume such coordinates, but the question of how the sensory system could derive these values is given no attention.     

Perceptual priming is not a necessary consequence of semantic classification of pictures

Four experiments investigated how repetition priming of object recognition is affected by the task performed in the prime and test phases. In Experiment 1 object recognition was tested using both vocal naming and two different semantic decision tasks (whether or not objects were manufactured, and whether or not they would be found inside the house). Some aspects of the data were inconsistent with contemporary models of object recognition. Specifically, object priming was eliminated with some combinations of prime and test tasks, and there was no evidence of perceptual (as opposed to conceptual or response) priming in either semantic classification task, even though perceptual identification of the objects is required for at least one of these tasks. Experiment 2 showed that even when perceptual demands were increased by brief presentation, the inside task showed no perceptual priming. Experiment 3 showed that the inside task did not appear to be based on conceptual priming either, as it was not primed significantly when the prime decisions were made to object labels. Experiment 4 showed that visual sensitivity could be restored to the inside task following practice on the task, supporting the suggestion that a critical factor is whether the semantic category is preformed or must be computed. The results show that the visual representational processes revealed by object priming depend crucially on the task chosen.     

Stereotype priming in face recognition: interactions between semantic and visual information in face encoding

The accuracy with which previously unfamiliar faces are recognised is increased by the presentation of a stereotype-congruent occupation label [Klatzky, R. L., Martin, G. L., & Kane, R. A. (1982a). Semantic interpretation effects on memory for faces. Memory & Cognition, 10, 195-206; Klatzky, R. L., Martin, G. L., & Kane, R. A. (1982b). Influence of social-category activation on processing of visual information. Social Cognition, 1, 95-109]. For example, providing the label 'criminal' both during encoding and test improves recognition for previously unfamiliar faces that look like the stereotypical criminal. Experiments 1 and 2 both replicate this effect and show that the label exerts its influence during the encoding of stereotypical faces and has little influence at test. These findings indicate that semantic information that is congruent with novel stereotypical faces facilitates their encoding.     

Effects of semantic priming on visual encoding of pictures

We investigated the effects of semantic priming on initial encoding of briefly presented pictures of objects and scenes. Pictures in four experiments were presented for varying durations and were followed immediately by a mask. In Experiments 1 and 2, pictures of simple objects were either preceded or not preceded by the object's category name (e.g., dog). In Experiment 1 we measured immediate object identification; in Experiment 2 we measured delayed old/new recognition in which targets and distractors were from the same categories. In Experiment 3 naturalistic scenes were either preceded or not preceded by the scene's category name (e.g., supermarket). We measured delayed recognition in which targets and distractors were described by the same category names. In Experiments 1-3, performance was better for primed than for unprimed pictures. Experiment 4 was similar to Experiment 2 in that we measured delayed recognition for simple objects. As in Experiments 1-3, a prime that preceded the object improved subsequent memory performance for the object. However, a prime that followed the object did not affect subsequent performance. Together, these results imply that priming leads to more efficient information acquisition. We offer a picture-processing model that accounts for these results. The model's central assumption is that knowledge of a picture's category (gist) increases the rate at which visual information is acquired from the picture.     

跨通道语义启动对视觉注意的影响

采用生活中的真实客体,考察了跨通道语义相关性对视觉注意的影响以及跨通道促进的时程。结合启动范式和点探测范式,实验1发现在听觉启动600ms后,被试对高相关视觉刺激的反应比对低相关刺激的反应更快,而在视觉启动下没有发现启动效应。实验2发现在启动刺激呈现900ms后跨通道启动效应消失。研究证明了基于先前经验的视、听语义相关能够促进视觉的选择性注意。     

Lexical but not semantic priming in Alzheimer's disease.

The hypothesis that patients with Alzheimer's disease (AD) have a disturbance in semantic processing was tested using a new lexical-priming task, threshold oral reading. Healthy elderly controls showed significant effects of priming for word pairs that are associatively related (words that reliably co-occur in word association tests) and for word pairs that are semantically related (high-frequency exemplars that belong to the same superordinate category but are not high-frequency associates). AD patients showed effects of priming for associatively related words but not for word pairs that are related only by shared semantic features. These results are consistent with the hypothesis that semantic processing is impaired in AD and suggest that independent networks of relationships among words and among concepts in semantic memory may be differentially disrupted with various forms of brain damage.     

Identity and semantic negative priming in rapid serial visual presentation streams

In selective attention tasks, the efficiency of processing concurrently presented target and distractor stimuli in a given display is often influenced by the relationship these stimuli have with those in the previous display. When a to-be-attended target on a current trial (the probe trial) matches the ignored, non-target distractor on a previous trial (the prime trial), a response to the target is typically delayed compared with when the two stimuli are not associated. This negative priming (NP) phenomenon has been observed in numerous studies with traditional NP tasks presenting the target and distractor simultaneously in both the prime and probe trial couplets. Here, however, in four experiments using a mixture of stimulus types (letters, digits, English number words, and logographic Chinese number words), target and distractor stimuli were temporally separated in two rapid serial visual presentation (RSVP) streams instead of concurrently presented. The findings provide a conceptual replication and substantial extension of a recent study by Wong (Plos One, 7, e37023, 2012), and suggest that active suppression of irrelevant distracting information is a more ubiquitous form of cognitive control than previously thought.     

Preparation for a forthcoming task is sufficient to produce subsequent shift costs

Shifting from one task to another is associated with significant costs. Recently, it has been questioned whether the mere preparation for a forthcoming task, without the task’s actually being executed, is sufficient to establish a new task set that results in shift costs when the execution of a task other than the prepared task is required. In a go/no-go study, it is shown that the mere preparation for a task is sufficient to produce shift costs, but only under conditions that encourage participants to engage in advance preparation for a precued task despite the possibility that the execution of this task will not always be required, because of occasional no-go trials. In addition, considerable reductions of shift costs after go trials could be observed under these conditions. When such a motivating context was not provided, only negligible shift costs were observed after a no-go trial, indicating that no task-set configuration had taken place without the need to perform the task. Furthermore, under these conditions, prolonging the preparation interval resulted in reaction time benefits that were similar for task shifts and repetitions, again indicating that no active task-set configuration took place.     

On visual access to letter case and lexical/semantic information

Four experiments were designed to investigate automatic processing of letter case and lexical/ semantic information under forward and backward masking conditions that disallowed a visible image. Stimulus displays were letter string pairs; the letter case for each pair matched or mismatched, and the relationship between the two strings within pairs varied. Experiment I required direct Same-Different responses to stimulus pairs, and the results indicate that tasks requiring direct responses to stimulus inputs cannot distinguish between conscious response biases and unconscious use of information. Experiments 2 and 3 employed an indirect index of automatic prerecognition analyses of verbal-linguistic parameters and showed that, with 30-msec pre- and postmasked presentations, letter case, orthographic regularity, and lexical/semantic information are all analyzed in unconscious operations. Experiment 4 demonstrated that, under the viewing conditions of Experiments 2 and 3, subjects had no awareness of the stimulus input.     

Attentional engagement is not sufficient to prevent spatial capture

What conditions, if any, can fully prevent attentional capture (i.e., involuntary allocation of spatial attention to an irrelevant object) has been a matter of debate. In a previous study, Folk, Ester, and Troemel (Psychonomic Bulletin & Review 16:127–132, 2009) suggested that attentional capture can be blocked entirely when attention is already engaged in a different object. This conclusion relied on the finding that in a search for a known-color target in a rapid serial visual presentation stream, a peripheral distractor with the target color did not further impair target identification performance when a distractor also with the target color that appeared in the stream had already captured attention. In the present study, we argue that this conclusion is unwarranted, because the effects of the central and peripheral distractors could not be disentangled. In order to isolate the effect of the peripheral distractor, we introduced a distractor–target letter compatibility manipulation. Our results showed that the peripheral distractor summoned attention, irrespective of whether attention had just been engaged. We conclude that neither spatially focused attention nor attentional engagement is sufficient to prevent attentional capture.     

Repetition priming in visual search: Episodic retrieval,not feature priming

Previous research has shown that when the targets of successive visual searches have features in common, response times are shorter. However, the nature of the representation underlying this priming and how priming is affected by the task remain uncertain. In four experiments, subjects searched for an odd-sized target and reported its orientation. The color of the items was irrelevant to the task. When target size was repeated from the previous trial, repetition of target color speeded the response. However, when target size was different from that in the previous trial, repetition of target color slowed responses, rather than speeding them. Our results suggest that these priming phenomena reflect the same automatic mechanism as the priming of pop-out reported by Maljkovic and Nakayama (1994). However, the crossover interaction between repetition of one feature and another rules out Maljkovic and Nakayama's (1994) theory of independent potentiation of distinct feature representations. Instead, we suggest that the priming pattern results from contact with an episodic memory representation of the previous trial.     

Semantic priming,not repetition priming,is to blame for false hearing

Contextual and sensory information are combined in speech perception. Conflict between the two can lead to false hearing, defined as a high-confidence misidentification of a spoken word. Rogers, Jacoby, and Sommers (Psychology and Aging, 27(1), 33–45, 2012) found that older adults are more susceptible to false hearing than are young adults, using a combination of semantic priming and repetition priming to create context. In this study, the type of context (repetition vs. sematic priming) responsible for false hearing was examined. Older and young adult participants read and listened to a list of paired associates (e.g., ROW–BOAT) and were told to remember the pairs for a later memory test. Following the memory test, participants identified words masked in noise that were preceded by a cue word in the clear. Targets were semantically associated to the cue (e.g., ROW–BOAT), unrelated to the cue (e.g., JAW–PASS), or phonologically related to a semantic associate of the cue (e.g., ROW–GOAT). How often each cue word and its paired associate were presented prior to the memory test was manipulated (0, 3, or 5 times) to test effects of repetition priming. Results showed repetitions had no effect on rates of context-based listening or false hearing. However, repetition did significantly increase sensory information as a basis for metacognitive judgments in young and older adults. This pattern suggests that semantic priming dominates as the basis for false hearing and highlights context and sensory information operating as qualitatively different bases for listening and metacognition.     

Crossmodal semantic priming by naturalistic sounds and spoken words enhances visual sensitivity

We propose a multisensory framework based on Glaser and Glaser's (1989) general reading-naming interference model to account for the semantic priming effect by naturalistic sounds and spoken words on visual picture sensitivity. Four experiments were designed to investigate two key issues: First, can auditory stimuli enhance visual sensitivity when the sound leads the picture as well as when they are presented simultaneously? And, second, do naturalistic sounds (e.g., a dog's "woofing") and spoken words (e.g., /d?g/) elicit similar semantic priming effects? Here, we estimated participants' sensitivity and response criterion using signal detection theory in a picture detection task. The results demonstrate that naturalistic sounds enhanced visual sensitivity when the onset of the sounds led that of the picture by 346 ms (but not when the sounds led the pictures by 173 ms, nor when they were presented simultaneously, Experiments 1-3A). At the same SOA, however, spoken words did not induce semantic priming effects on visual detection sensitivity (Experiments 3B and 4A). When using a dual picture detection/identification task, both kinds of auditory stimulus induced a similar semantic priming effect (Experiment 4B). Therefore, we suggest that there needs to be sufficient processing time for the auditory stimulus to access its associated meaning to modulate visual perception. Besides, the interactions between pictures and the two types of sounds depend not only on their processing route to access semantic representations, but also on the response to be made to fulfill the requirements of the task.     

Inhibited prime-trial distractor responses solely produce the visual spatial negative priming effect

Responding to a target??s current (probe trial) location is slower when it appears at a former distractor-occupied position (i.e., ignored-repetition [IR] trial), relative to when it arises at a new location (i.e., control trial). This RT(IR) > RT(Control) inequality defines the spatial negative priming (SNP) effect in latency terms. It is uncertain whether the elevated RT(IR) is due to the inhibition of the distractor-occupied location or to the inhibition of this location??s assigned manual response (SNP locus issue). The main aim here was to examine the SNP locus issue. Notably, our SNP design used centrally presented visual events and included having two locations share a common response (many:1 location-to-response mapping) and the use of informative (70?% validity) or uninformative probe-trial response cues. The many:1 mapping trials allowed for the detection of location and response inhibition presence. Results showed that the latter, but not the former, causes inhibitory aftereffects (e.g., SNP) following uninformative response cues. Consistent with this finding, when the informative response cue was valid and was assigned to the many:1 probe response that had just served as the prime distractor response, inhibitory aftereffects were eliminated, when the probe target appeared at the prime distractor position (IR trial) or at a new location (distractor?Cresponse repeat trial). Blocked retrieval of stored distractor-processing representations was proposed as the mechanism for inhibitory aftereffect prevention.