Visual memory for moving scenes

In the present study, memory for picture boundaries was measured with scenes that simulated self-motion along the depth axis. The results indicated that boundary extension (a distortion in memory for picture boundaries) occurred with moving scenes in the same manner as that reported previously for static scenes. Furthermore, motion affected memory for the boundaries but this effect of motion was not consistent with representational momentum of the self (memory being further forward in a motion trajectory than actually shown). We also found that memory for the final position of the depicted self in a moving scene was influenced by properties of the optical expansion pattern. The results are consistent with a conceptual framework in which the mechanisms that underlie boundary extension and representational momentum (a) process different information and (b) both contribute to the integration of successive views of a scene while the scene is changing.     

Visual memory for moving scenes

In the present study, memory for picture boundaries was measured with scenes that simulated self-motion along the depth axis. The results indicated that boundary extension (a distortion in memory for picture boundaries) occurred with moving scenes in the same manner as that reported previously for static scenes. Furthermore, motion affected memory for the boundaries but this effect of motion was not consistent with representational momentum of the self (memory being further forward in a motion trajectory than actually shown). We also found that memory for the final position of the depicted self in a moving scene was influenced by properties of the optical expansion pattern. The results are consistent with a conceptual framework in which the mechanisms that underlie boundary extension and representational momentum (a) process different information and (b) both contribute to the integration of successive views of a scene while the scene is changing.     

Visual search of common scenes

A visual search reaction time task was used to examine the relationships among encoding, comparison, and search processes. Targets, either pictures of objects or their names, were briefly presented and followed, at stimulus onset asynchronies (SOAs) ranging from 200 to 2000 ms, by pictorial scenes having a 50% probability of containing the target. Generally, subjects responded more rapidly with picture than word targets, this difference diminishing at longer SOAs. Searches appeared to be restricted to certain portions of the scene depending on the congruency between the target and the scene. The sequence of decisions in the search task was discussed.     

Visual search for arbitrary objects in real scenes

How efficient is visual search in real scenes? In searches for targets among arrays of randomly placed distractors, efficiency is often indexed by the slope of the reaction time (RT) × Set Size function. However, it may be impossible to define set size for real scenes. As an approximation, we hand-labeled 100 indoor scenes and used the number of labeled regions as a surrogate for set size. In Experiment 1, observers searched for named objects (a chair, bowl, etc.). With set size defined as the number of labeled regions, search was very efficient (~5 ms/item). When we controlled for a possible guessing strategy in Experiment 2, slopes increased somewhat (~15 ms/item), but they were much shallower than search for a random object among other distinctive objects outside of a scene setting (Exp. 3: ~40 ms/item). In Experiments 4–6, observers searched repeatedly through the same scene for different objects. Increased familiarity with scenes had modest effects on RTs, while repetition of target items had large effects (>500 ms). We propose that visual search in scenes is efficient because scene-specific forms of attentional guidance can eliminate most regions from the “functional set size” of items that could possibly be the target.     

Competition between two memory traces for long-term recognition memory

Previous studies investigating the processes which underlie memory consolidation focused almost exclusively on isolated learning events. Here I studied the competition of two similar memory traces for consolidation non-conditioned recognition memory in adult male C57BL/6JOlaHsd mice using the olfactory cues based social discrimination procedure. My results show that the interference phenomena that cause forgetting are time-dependent, and that retroactive interference can be discriminated from proactive interference. Furthermore, both types of interference can be suppressed by subcutaneous anisomycin treatment immediately after presentation of the interference stimulus. These findings imply that interference phenomena, which result from the competition of two similar memory traces for long-term recognition memory, are related to the progress of memory consolidation and linked to protein synthesis.     

Visual search has memory

By monitoring subjects' eye movements during a visual search task, we examined the possibility that the mechanism responsible for guiding attention during visual search has no memory for which locations have already been examined. Subjects did reexamine some items during their search, but the pattern of revisitations did not fit the predictions of the memoryless search model. In addition, a large proportion of the refixations were directed at the target, suggesting that the revisitations were due to subjects' remembering which items had not been adequately identified. We also examined the patterns of fixations and compared them with the predictions of a memoryless search model. Subjects' fixation patterns showed an increasing hazard function, whereas the memoryless model predicts a flat function. Lastly, we found no evidence suggesting that fixations were guided by amnesic covert scans that scouted the environment for new items during fixations. Results do not support the claims of the memoryless search model, and instead suggest that visual search does have memory.     

Visual search in scenes involves selective and nonselective pathways

How does one find objects in scenes? For decades, visual search models have been built on experiments in which observers search for targets, presented among distractor items, isolated and randomly arranged on blank backgrounds. Are these models relevant to search in continuous scenes? This article argues that the mechanisms that govern artificial, laboratory search tasks do play a role in visual search in scenes. However, scene-based information is used to guide search in ways that had no place in earlier models. Search in scenes might be best explained by a dual-path model: a 'selective' path in which candidate objects must be individually selected for recognition and a 'nonselective' path in which information can be extracted from global and/or statistical information.     

Binding actions and scenes in visual long-term memory

How does visual long-term memory store representations of different entities (e.g., objects, actions, and scenes) that are present in the same visual event? Are the different entities stored as an integrated representation in memory, or are they stored separately? To address this question, we asked observers to view a large number of events; in each event, an action was performed within a scene. Afterward, the participants were shown pairs of action–scene sets and indicated which of the two they had seen. When the task required recognizing the individual actions and scenes, performance was high (80 %). Conversely, when the task required remembering which actions had occurred within which scenes, performance was significantly lower (59 %). We observed this dissociation between memory for individual entities and memory for entity bindings across multiple testing conditions and presentation durations. These experiments indicate that visual long-term memory stores information about actions and information about scenes separately from one another, even when an action and scene were observed together in the same visual event. These findings also highlight an important limitation of human memory: Situations that require remembering actions and scenes as integrated events (e.g., eyewitness testimony) may be particularly vulnerable to memory errors.     

Mental relaxation improves long-term incidental visual memory

Experimental evidence has linked increased arousal to enhanced memory retention. There is also evidence that procedures reducing arousal, i.e., mental relaxation, might improve memory, but conflicting results have been reported. To clarify this issue, we studied the effects of a single session of relaxation training on incidental visual long-term memory. Thirty-two relaxation-naive subjects viewed 280 slides without being told that there would be subsequent memory testing. Afterwards, subjects listened to a 12 min relaxation tape; 16 subjects relaxed by following the instructions (relaxation group), and the other 16 subjects pressed a button whenever a body part was mentioned (control group). While listening to the relaxation tape, high frequency heart rate variability (HRV) was greater and low frequency HRV was lower in the relaxation group, implying effective relaxation and increasing parasympathetic activation. The relaxation group had superior memory retention 4 weeks later (p = .004), indicating enhancement of long-term memory performance. This effect could not be explained by retroactive interference experienced in the control group because short-term memory performance immediately after the tape was slightly better in the control group. Retention of materials acquired after the relaxation session remained unaffected, suggesting relaxation has retrograde effects on memory consolidation. Our data demonstrate a favorable influence of relaxation on at least this aspect of learning. Our data also extend previous knowledge on the beneficial effects of ascending parasympathetic stimulation on memory retention in that enhanced long-term memory consolidation may also occur in the presence of central and descending parasympathetic activation triggered by willful psychomotor activity.     

Sequential search processes in long-term memory

In an experiment employing the symbol-element recognition task (Mohs, Wescourt, & Atkinson, 1975), subjects first learned six lists consisting of four words (elements) each. Each list was associated with a unique consonant (symbol). Subsequently, on each of a series of test trials, subjects were presented with one, two, or four symbol-element pairs. A positive response was required if all test words were correctly paired with their associated consonants and a negative response if any one test word was incorrectly paired with a consonant. Of primary concern was the way reaction time (RT) varied with number of pairs presented, the type of response required, and, on negative trials, the position of the mismatched pair in the test display. RT increased with the number of pairs presented on a trial and the increase was greater for positive than for negative trials. For negative pair trials, RT increased with the distance of the mismatched pair from the top of the test display. On negative trials in which the top pair in the test display was the mismatched pair, RT increased with the total number of pairs presented on the trial. A serial, probabilistic order of processing model is proposed to account for these results, and applications of the model to other paradigms are discussed.     

Organization and long-term memory search

A recognition RT paradigm was used to assess a number of plausible search strategies in LTM for categorized lists. List length was determined by factorially combining two, three, or five categories with two, three, or five words per category, and test items could be one of four types: (1) positive, (2) a repeated positive, (3) a related negative, or (4) an unrelated negative. It was found that RT increased linearly with category size for both positive and related negatives (about 30-40 msec/item); whereas the increase was much smaller for the unrelated negatives, especially for three and five categories (about 9 msec/item). With an increase in the number of categories, RT increased at the rate of about 40 msec/category for all three test items. A theory of .high-speed scanning for categorized material was proposed in which a serial and exhaustive search of the categories, is first undertaken. If a positive category match is found, a serial and exhaustive search within the contents of the positive category is initiated; if no category match is found, the search is simply terminated. Some evidence was presented that categories recently probed may provide for a short-circuiting of the category search.     

Developmental changes in self-corrected elaboration effects on incidental memory

Abstract:  Two experiments were carried out to investigate the changes across age groups in the effects of self-corrected elaboration on incidental memory. Each participant performed an orienting task involving three conditions: self-corrected, self-generated and experimenter-provided elaboration. The orienting task was followed by free recall tests. In Experiment 1, the participants were sixth-grade and second-grade students. For sixth-grade students the self-corrected elaboration led to a better free recall than the other two elaborations, whereas for the second-grade students, no difference was observed between any of the three elaborations. In Experiment 2, using a longer word list than that in Experiment 1, the participants were undergraduates. The self-corrected and self-generated elaborations led to a better free recall than the experimenter-provided elaboration, and no difference between the former two elaborations was observed. The results obtained from these two experiments were interpreted as showing that the effectiveness of a self-corrected elaboration depends on the participants' age.     

Evidence that baroreflex feedback influences long-term incidental visual memory in men

Sympathetic nervous system (SNS) activity at the time of acquisition is associated with human memory. However, rather than SNS activity per se, it may be afferent baroreflex feedback that is responsible for this effect. A pharmacological design was employed to unload (SNP, sodium nitro-prusside) and load (norepinephrine) baroreceptors. In addition to two placebo periods, epinephrine and esmolol (a peripherally acting beta1-blocker) served as control conditions for altered cardiac perception. During drug infusion blood pressure, heart rate, and perception of heartbeat were tested. Twenty-four healthy men were participated. The participants viewed emotional slides while their electromyographic eye blink responses to random noise bursts were measured (affective startle modulation paradigm) to determine potential drug impact on emotional processing. Subjects were not informed that memory testing would take place after 4 weeks. Drugs did not impact startle, thus indicating unbiased emotional processing at the time of acquisition. Norepinephrine had no effect on heartbeat perception, but improved (p = .002) recognition memory. SNP (p = .0001) increased heartbeat perception but impaired (p = .038) recognition memory. Epinephrine, on the other hand, increased heartbeat perception (p = .0001) yet did not impair but partially improve memory (effect on high arousing pictures only: p = .05). Heartbeat perception in the placebo condition did not correlate with recognition memory (p's > .5). We suggest that baroreflex unloading, with subsequent feedback activation of the SNS, impairs long-term incidental visual recognition memory in humans while baroreflex loading enhances it. Further, we propose that these memory effects are neither secondary to cardiac sensations that accompany SNS activation nor to altered emotional picture processing at the time of acquisition.     

The target effect: Visual memory for unnamed search targets

Search targets are typically remembered much better than other objects even when they are viewed for less time. However, targets have two advantages that other objects in search displays do not have: They are identified categorically before the search, and finding them represents the goal of the search task. The current research investigated the contributions of both of these types of information to the long-term visual memory representations of search targets. Participants completed either a predefined search or a unique-object search in which targets were not defined with specific categorical labels before searching. Subsequent memory results indicated that search target memory was better than distractor memory even following ambiguously defined searches and when the distractors were viewed significantly longer. Superior target memory appears to result from a qualitatively different representation from those of distractor objects, indicating that decision processes influence visual memory.     

Visual memory and visual perception: when memory improves visual search

This study examined the relationship between memory and perception in order to identify the influence of a memory dimension in perceptual processing. Our aim was to determine whether the variation of typical size between items (i.e., the size in real life) affects visual search. In two experiments, the congruency between typical size difference and perceptual size difference was manipulated in a visual search task. We observed that congruency between the typical and perceptual size differences decreased reaction times in the visual search (Exp. 1), and noncongruency between these two differences increased reaction times in the visual search (Exp. 2). We argue that these results highlight that memory and perception share some resources and reveal the intervention of typical size difference on the computation of the perceptual size difference.     

Incidental visual memory for objects in scenes

Three experiments were conducted to investigate the existence of incidentally acquired, long-term, detailed visual memory for objects embedded in previously viewed scenes. Participants performed intentional memorization and incidental visual search learning tasks while viewing photographs of real-world scenes. A visual memory test for previously viewed objects from these scenes then followed. Participants were not aware that they would be tested on the scenes following incidental learning in the visual search task. In two types of memory tests for visually specific object information (token discrimination and mirror-image discrimination), performance following both the memorization and visual search conditions was reliably above chance. These results indicate that recent demonstrations of good visual memory during scene viewing are not due to intentional scene memorization. Instead, long-term visual representations are incidentally generated as a natural product of scene perception.     

Visual and semantic factors in recognition from long-term memory

In recognition tests, physical and semantic relationships between targets and distractors have been shown, in separate manipulations, to affect the latency of subject's decision. Recognition was tested for distractors which were visually similar or dissimilar to targets and which belonged to the target categories or to nontarget categories in order to examine the interaction of these dimensions. Rejection latency was longer for target category than for nontarget category distractors. Latency was also longer for visually similar than visually dissimilar distractors, but only when combined with target category probes. This interaction can be explained by the hypothesis that word recognition depends on the analysis of several dimensions of the probe stimulus, and rejection can occur before all such analyses have been completed.