Self-discrepancies and emotional vulnerability: how magnitude, accessibility, and type of discrepancy influence affect

Two studies examined whether the type of emotional change experienced by individuals is influenced by the magnitude and accessibility of the different types of self-discrepancies they possess. In both studies, subjects filled out a measure of self-discrepancy a few weeks prior to the experimental session. Subjects were asked to list up to 10 attributes each for different self-states--their actual self, their ideal self (their own or others' hopes and goals for them), and their ought self (their own or others' beliefs about their duty and obligations). Magnitude of self-discrepancy was calculated by comparing the attributes in the actual self to the attributes in either the ideal self or the ought self, with the total number of attribute pairs that matched being subtracted from the total number of attribute pairs that mismatched. In Study 1, subjects were asked to imagine either a positive event or a negative event and were then given a mood measure and a writing-speed task. Subjects with a predominant actual:ideal discrepancy felt more dejected (e.g., sad) and wrote more slowly in the negative event condition than in the positive event condition, whereas subjects with a predominant actual:ought discrepancy, if anything, felt more agitated (e.g., afraid) and wrote more quickly in the negative event condition. In Study 2, subjects were selected who were either high in both kinds of discrepancies or low in both. Half of the subjects in each group were asked to discuss their own and their parents' hopes and goals for them (ideal priming), and the other half were asked to discuss their own and their parents' beliefs concerning their duty and obligations (ought priming). For high-discrepancy subjects, but not low-discrepancy subjects, ideal priming increased their dejection whereas ought priming increased their agitation. The implications of these findings for identifying cognitive-motivational factors that may serve as vulnerability markers for emotional problems is discussed.     

Interaction of task readiness and automatic retrieval in task switching: Negative priming and competitor priming

When subjects switch between tasks, performance is slower after a task switch than after a task repetition, even when preparation time is long. We report two experiments that support the idea that a large part of these residual task shift costs can be due to stimulus-cued retrieval of previous task episodes. We demonstrate that there are two different factors at work: (1) facilitation of response to the current distractor stimulus, appropriate to the previously relevant, competing task (competitor priming), and (2) impaired processing of previously suppressed responses (negative priming). Negative priming was contingent on the size of the stimulus set, suggesting that distractor suppression comes into effect only if the distractors are highly activated. Importantly, both types of interference interacted with task readiness: Whereas in the nondominant task (picture naming), switch and nonswitch trials were equally affected, the dominant task (word reading) showed priming effects on switch trials only. Thus, the retrieval of previous processing episodes has a selective impact on situations in which task competition is high.     

The effect of memory load on negative priming: An individual differences investigation

The effect of a verbal (Experiment 1) and a nonverbal (Experiment 2) memory load on negative priming was investigated by employing a concurrent memory task with a letter naming task. Across both experiments, negative priming was reliable only under conditions of zero memory load, suggesting that the processes that contribute to negative priming are resource demanding and dependent on a domain-free resource pool. Individual differences in negative priming were observed, such that high working memory capacity subjects showed reliable negative priming whereas low working memory capacity subjects did not. The results suggest that the negative priming effect results from allocation of controlled attention and that individual differences in working memory capacity correspond to the ability to efficiently handle irrelevant information.     

Asymmetric switch cost and backward inhibition: Carryover activation and inhibition in switching between tasks of unequal difficulty.

Asymmetric switch cost, observed when switching between tasks varying in difficulty, shows that the difference between repeat and switch trials is greater when switching to the easier task. Early explanations of this effect attributed this pattern to both positive priming of the difficult task and negative priming of the easier task, but more recent models have focused only on activation processes. The role of inhibition in asymmetric switch cost was examined using backward inhibition, a more direct measure of task-set inhibition. The results indicated asymmetric backward inhibition, with greater sequential inhibition of the easier task (i.e., easy-difficult-easy sequences). Switch costs, however, showed both typical and reversed asymmetry (greater cost when switching from the easy to the difficult task), depending on the relative difficulty of task pairs. This pattern of results indicates that switch costs are attributable to both activation and inhibition processes.     

Conditions of error priming in number-fact retrieval

Analysis of errors in simple multiplication has shown that answers retrieved on previous trials are initially inhibited (negative error priming) but later are promoted as errors to subsequent problems (positive error priming). Two experiments investigated whether error priming is associated either with problem-specific retrieval processes or with representations of answers that can be manipulated independently of problems. In Experiment 1, answers were primed by visually presenting products for 200 msec prior to problems. Correct-answer primes facilitated retrieval, related-incorrect primes interfered with retrieval more than unrelated primes, and both effects were greater for more difficult problems. Primes affected only the trial on which they were presented, however, whereas both negative and positive error priming from previous problems were observed across trials. In Experiment 2, subjects named and retrieved multiplication products on alternating trials. Just-named products were inhibited as errors to the following multiplication problem (i.e., negative error priming), but, compared to positive priming from previous retrieved products, positive error priming from previously named numbers was weak. The results indicate that positive error priming is due mainly to an encoding or retrieval bias produced by previous problems, whereas negative error priming entails suppression, or de-selection, of answer representations.     

Affective Priming Effects in the Left and Right Cerebral Hemispheres in Patients With Alzheimer's Disease

Alzheimer’s disease (AD) patients and control subjects were tested in an affective priming paradigm associated with an affective discrimination task. Two pictures, one affectively positive or affectively negative and the other neutral, were presented simultaneously in the right and in the left visual fields; the participants had to decide which of the two pictures was the most affectively positive or negative. The target pictures were preceded by a prime picture that was either affectively positive, affectively negative, or neutral. The principal result was the observation, in AD patients as well as in control subjects, of negative affective priming effects for targets presented in the right hemisphere, and of positive affective priming effects for targets presented in the left hemisphere. The presence of affective priming effects suggests that AD patients have no particular deficit in the automatic activation of emotional information; the fact that priming effects were also observed for targets presented in the left hemisphere showed that AD patients probably have no left hemisphere deficit in the automatic activation of emotional information. However, in AD patients, affective priming effects were significant with negative targets but not with positive targets, which could suggest that AD patients processed positive targets in a more semantic way than negative targets.     

Task switches under Go/NoGo conditions and the decomposition of switch costs

Alternating switches between two simple S-R tasks are combined with Go/NoGo tasks. Non-switches after Go trials are assumed to selectively profit from stimulus driven repetition benefits, whereas switches after NoGo trials are assumed to be selectively delayed by stimulus driven negative priming. Intentionally driven reconfiguration costs are assessed by RT differences between switches after Go trials (no negative priming) and non-switches after NoGo trials (no repetition benefits). Experiment 1 indicates that with short preparation time repetition benefits, negative priming costs, and intentional components contribute approximately additively to switch costs. Experiment 2 confirms that the delay of switches after NoGo trials is indeed due to negative priming. Experiments 3 and 4 show that repetition benefits and intentional components of switch costs are properly assessed only if the settings assure that participants reconfigure the required task set in NoGo as well as Go trials.     

A transfer analysis of the repetition effect in the lexical and ambiguity decision tasks

Two experiments were performed in an attempt to evaluate explanations of repetition priming-the facilitation observed when the same word is processed a second time in the same task. One task employed was lexical decision (word/nonword) and the other was ambiguity decision (ambiguous/ unambiguous). In the first experiment, transfer on a lexical decision task was measured following either a lexical decision or an ambiguity decision. When the identical lists were processed in the first phase for lexical and ambiguity decision, equal repetition effects were obtained on lexical decision. However, when the ambiguity task was presented without nonwords, no repetition priming occurred. In a second experiment, the within-task repetition effect was large for the ambiguity decision, whereas no transfer was obtained from lexical decision to ambiguity decision. The results were interpreted as being consistent with a transfer-appropriate processing account of repetition priming.     

Awareness of the influence as a determinant of assimilation versus contrast

In the present study, subjects had to generate an evaluative judgment about a target person on the basis of his behaviour that had both positive and negative implications. In a previous phase of the study that was ostensibly unrelated to the judgment task, the relevant trait categories were primed. Subsequently, half of the subjects were reminded of the priming episode. Consistent with earlier research (e.g. Lombardi, Higgins and Bargh, 1987; Newman and Uleman, 1990) that used memory of the priming events as a correlational measure, a contrast effect was found under the ‘reminding’ condition and assimilation resulted when subjects were not reminded of the priming episode. This pattern of results is interpreted as the consequence of corrective influences.     

The Relationship Between Cognitive Ability and Positive and Negative Priming in Identity and Spatial Priming Tasks

The authors examined whether stimulus activation and inhibition in the identity priming task are related to the temporal lobe, and whether these processes in the spatial priming task are related to the parietal lobe. Forty participants performed spatial and identity positive and negative priming tasks, the Vandenberg Mental Rotation task, and the Digit Span task. Both men and women showed significant positive and negative priming in the identity and spatial tasks with no gender difference. The magnitude of identity positive priming was predicted by the Digit Span task, and the magnitude of spatial positive priming was predicted by the mental rotation task. Only women showed a correlation between spatial ability and spatial negative priming. The results are partially consistent with the dorsal-ventral model of cognitive inhibition.     

The relationship between cognitive ability and positive and negative priming in identity and spatial priming tasks

The authors examined whether stimulus activation and inhibition in the identity priming task are related to the temporal lobe, and whether these processes in the spatial priming task are related to the parietal lobe. Forty participants performed spatial and identity positive and negative priming tasks, the Vandenberg Mental Rotation task, and the Digit Span task. Both men and women showed significant positive and negative priming in the identity and spatial tasks with no gender difference. The magnitude of identity positive priming was predicted by the Digit Span task, and the magnitude of spatial positive priming was predicted by the mental rotation task. Only women showed a correlation between spatial ability and spatial negative priming. The results are partially consistent with the dorsal-ventral model of cognitive inhibition.     

Contextual modulation of prime response retrieval processes: Evidence from auditory negative priming

Contextual similarity between learning and test phase has been shown to be beneficial for memory retrieval. Negative priming is known to be caused by multiple processes; one of which is episodic retrieval. Therefore, the contextual similarity of prime and probe presentations should influence the size of the negative priming effect. This has been shown for the visual modality. In Experiment 1, an auditory four-alternative forced choice reaction time task was used to test the influence of prime-probe contextual similarity on negative priming and the processes underlying the modulation by context. The negative priming effect was larger when the auditory context was repeated than when it was changed from prime to probe. The modulation by context was exclusively caused by an increase in prime response retrieval errors in ignored repetition trials with context repetition, whereas repeating only the context but not the prime distractor did not lead to an increase in prime response retrieval. This exact pattern of results was replicated in Experiment 2. The findings suggest that contextual information is integrated with prime distractor and response information. Retrieval of the previous episode, including prime distractor, prime response, and context (event file), can be triggered when the former prime distractor is repeated, whereas a context cue alone does not retrieve the event file. This suggests an event file structure that is more complicated than its usually assumed binary structure.     

Negative emotional outcomes impair older adults’ reversal learning

In a typical reversal-learning experiment, one learns stimulus–outcome contingencies that then switch without warning. For instance, participants might have to repeatedly choose between two faces, one of which yields points whereas the other does not, with a reversal at some point in which face yields points. The current study examined age differences in the effects of outcome type on reversal learning. In the first experiment, the participants’ task was either to select the person who would be in a better mood or to select the person who would yield more points. Reversals in which face was the correct option occurred several times. Older adults did worse in blocks in which the correct response was to select the person who would not be angry than in blocks in which the correct response was to select the person who would smile. Younger adults did not show a difference by emotional valence. In the second study, the negative condition was switched to have the same format as the positive condition (to select who will be angry). Again, older adults did worse with negative than positive outcomes, whereas younger adults did not show a difference by emotional valence. A third experiment replicated the lack of valence effects in younger adults with a harder probabilistic reversal-learning task. In the first two experiments, older adults performed about as well as younger adults in the positive conditions but performed worse in the negative conditions. These findings suggest that negative emotional outcomes selectively impair older adults’ reversal learning.     

Negative emotional outcomes impair older adults' reversal learning

In a typical reversal-learning experiment, one learns stimulus-outcome contingencies that then switch without warning. For instance, participants might have to repeatedly choose between two faces, one of which yields points whereas the other does not, with a reversal at some point in which face yields points. The current study examined age differences in the effects of outcome type on reversal learning. In the first experiment, the participants' task was either to select the person who would be in a better mood or to select the person who would yield more points. Reversals in which face was the correct option occurred several times. Older adults did worse in blocks in which the correct response was to select the person who would not be angry than in blocks in which the correct response was to select the person who would smile. Younger adults did not show a difference by emotional valence. In the second study, the negative condition was switched to have the same format as the positive condition (to select who will be angry). Again, older adults did worse with negative than positive outcomes, whereas younger adults did not show a difference by emotional valence. A third experiment replicated the lack of valence effects in younger adults with a harder probabilistic reversal-learning task. In the first two experiments, older adults performed about as well as younger adults in the positive conditions but performed worse in the negative conditions. These findings suggest that negative emotional outcomes selectively impair older adults' reversal learning.     

Priming effects in prospective memory

Abstract

The objective of this study was to examine whether an increased activation of knowledge structures facilitates memory for future actions. Priming effects were manipulated by giving subjects a category fluency task for half of the target categories used in the subsequent prospective memory task. In this task, younger and older adults performed an action whenever an instance of a given semantic category occurred in the context of a free association task. The degree of retrieval support was varied by using typical and atypical category instances as targets. Although reliable priming effects were observed for both age groups, the magnitude of priming interacted with the degree of retrieval support. Older adults showed priming effects for typical targets only, whereas the opposite pattern of results was obtained for younger adults. These findings indicate that, in addition to retrieval-related factors, the operations performed at the time of planning also contribute to optimal prospective remembering.     

Evidence for the automatic evaluation of self-generated actions

The accuracy of simple actions is swiftly determined through specific monitoring brain systems. However, it remains unclear whether this evaluation is accompanied by a rapid and compatible emotional appraisal of the action that allows to mark incorrect actions as negative/bad and conversely correct actions as positive/good. In this study, we used a new method to decode the affective value of simple actions generated by participants during a standard Go/noGo task. Immediately after each Go/noGo action, participants responded to the valence of either a positive or a negative word. Results showed that False Alarms performed during the Go/noGo task led to a faster evaluative categorization of negative words relative to positive words. This action-word evaluative priming effect occurred when the interval between these two events was set to either 300 or 600ms, but not 1000ms. Finally, higher levels of trait anxiety were associated with a reduction of the evaluative priming effect. Our results suggest that simple actions are rapidly evaluated as positive or negative depending on the automatic monitoring of their perceived accuracy.     

Effects of prime task on affective priming by facial expressions of emotion

Priming of affective word evaluation by pictures of faces showing positive and negative emotional expressions was investigated in two experiments that used a double task procedure where participants were asked to respond to the prime or to the target on different trials. The experiments varied between-subjects the prime task assignment and the prime-target interval (SOA, stimulus onset asynchrony). Significant congruency effects (that is, faster word evaluation when prime and target had the same valence than when they were of opposite valence) were observed in both experiments. When the prime task oriented the subjects to an affectively irrelevant property of the faces (their gender), priming was observed at SOA 300 ms but not at SOA 1000 ms (Experiment 1). However, when the prime task assignment explicitly oriented the subjects to the valence of the face, priming was observed at both SOA durations (Experiment 2). These results show, first, that affective priming by pictures of facial emotion can be obtained even when the subject has an explicit goal to process a non-affective property of the prime. Second, sensitivity of the priming effect to SOA duration seems to depend on whether it is mediated by intentional or unintentional activation of the valence of the face prime.     

积极情绪对任务转换的影响

通过两个行为实验考察了积极情绪图片所诱发的情绪状态对任务转换的影响及其机制。研究任务是数字分类任务,分为保持和转换两个阶段。首先要求被试对靶刺激形成一定的习惯化反应,然后改变任务要求。实验1以53名大学生为被试,分别在积极情绪、消极情绪和中性条件下完成任务,发现在与中性条件相比时,积极情绪促进任务转换,消极情绪延缓任务转换。实验2以37名大学生为被试,增加了一种转换条件,考察积极情绪促进任务转换的心理原因,结果表明积极情绪因偏好新异刺激而促进任务转换     

Single‐prime negative priming in the shape‐matching task: Implications for the role of perceptual segmentation processes

Using the shape‐matching task developed by DeSchepper and Triesman (1996), Loula, Kourtzi, and Shiffrar (2000) demonstrated that negative priming only occurred in that task when minimal segmentation cues were available in the prime display. Loula et al. (2000) interpreted their results as revealing that negative priming in the shape‐matching task is directly caused by difficulty in segmenting the prime target from the prime distractor. We offer an alternative interpretation of their results, suggesting that a failure to observe negative priming when segmentation cues are present was incidental to the perceptual segmentation process. Instead, we provide evidence suggesting that an easier perceptual segmentation task contributes positive priming influences that makes a negative priming effect more difficult to observe. Once these positive priming influences are removed, we observed negative priming both when the perceptual segmentation task is trivial and when perceptual segmentation is not a component of the prime task at all.     

Priming cue encoding by manipulating transition frequency in explicitly cued task switching

Explicitly cued task switching with multiple cues per task permits three types of transitions: cue repetitions (cue and task repeat), task repetitions (cue changes but task repeats), and task alternations (cue and task change). The difference between task alternations and task repetitions can be interpreted as a switch cost, but its magnitude varies substantially across experiments. We investigated how switch cost is affected by transition frequency (how often subjects repeat and switch tasks) with an experiment in which each transition had a frequency of .70 in separate sessions. Switch cost was smallest when task alternations were frequent and largest when task repetitions were frequent. Mathematical modeling of the data indicated that the different “switch costs” reflected priming of cue encoding for frequent transitions. Interpretations of our findings based on automatic priming from memory retrieval of past transitions and strategic priming from transition expectancies are discussed.