Taking a bright view of negative priming in the light of dim stimuli: further evidence for memory confusion during episodic retrieval.

A same-different letter-matching task was used to examine the effects of stimulus intensity on negative priming, which is poorer performance when target letters have been presented as distractor letters on the immediately preceding trial. In Experiment 1, stimulus intensity was manipulated between-participants, whereas in Experiment 2, it varied randomly from trial-to-trial within-participants. In Experiment 1, negative priming was equivalent for both stimulus intensities. In Experiment 2, negative priming effects were larger for repeated intensity stimuli than for nonrepeated intensity stimuli, when stimulus intensity was dim. Furthermore, for repeated intensity stimuli, negative priming effects were enhanced when the overt response required to the stimulus was repeated from prime to probe trial. These results are consistent with the hypothesis that negative priming may be due to memory confusion, rather than to inhibition of the distractor stimuli.     

Brief presentations are sufficient for pigeons to discriminate arrays of same and different stimuli

Four pigeons first learned to discriminate 16-item arrays of same from different pictorial stimuli. They were then tested with reduced exposure to the pictorial arrays, brought about by changes in the stimulus viewing requirement under fixed-ratio (FR) and fixed-interval (FI) schedules. Increasing the FR requirement enhanced discriminative performance up to 10 pecks; increasing the FI requirement enhanced discriminative performance up to 5 s. Exposures to the stimulus arrays averaging only 2 s supported reliable discrimination. Pigeons thus discriminate same from different stimuli with considerable speed, suggesting that same-different discrimination behavior is of substantial adaptive significance.     

Pitch as a phonemic cue

Three experiments that were designed to determine how pitch information is represented in auditory memory are reported. A same-different reaction time was used in all three experiments. Previous experiments have interpreted the finding of faster “same” responses to acoustically identical pairs than to pairs that are phonemically identical but acoustically distinct as indicating that there is a memory that preserves auditory information. It has been assumed that this can be used to match “same” pairs only if the formant frequencies of the members of the pair are the same. In the first experiment, the size of this matching advantage for pairs with identical formant frequencies was not altered when the members of the pair were on different pitches. This indicates that pitch is represented separately from the formants at the auditory level. The second and third experiments used a bigger pitch difference when the pairs were on a different pitch, which, for one of the stimulus sets, resulted in a change in vowel quality but not in the identity of the consonant. In the other stimulus set, both phonemes of the syllable remained the same when presented on different pitches. The matching advantage was reduced when the stimuli were on different pitches for both stimulus sets. This indicates that a difference in pitch can prevent matching at the auditory level under some circumstances. An additional finding, a reduced residual matching advantage when the syllable changes, indicates that at least a syllable-length representation is held in auditory memory. The results are discussed with respect to how the representation in auditory memory might be used in the perception of speech produced by different speakers.     

Stimulus-specific processing consequences of pattern goodness

Two issues concerning the effects of visual pattern goodness on information processing time were investigated: the role of memory vs. encoding and the role of individual stimulus goodness vs. stimulus similarity. A sequential “same-different” task was used to provide differentiation of target item or memory effects from display item or encoding effects. Experiment 1 used four alternative stimuli in each block of trials. The results showed that good patterns were processed faster than poor patterns for both “same” and “different” responses. Furthermore, the goodness of the target item had a greater effect on reaction time than did the goodness of the display item, indicating that memory is more important than encoding in producing faster processing of good stimuli. Effects of interstimulus similarity on processing time were minimal, although isolation of good stimuli in a similarity space could explain many of the results. Experiment 2 replicated the results of Experiment 1, despite the fact that differences in similarity space had been minimized by using only two alternative stimuli in each block. In addition, the speed of processing a “same” pair was essentially independent of the particular alternative stimulus in a block. These results suggest that in this task, there is a processing advantage for good stimuli that is stimulus specific, with the effect operating primarily in memory.     

Are three-sample tasks less sensitive than two-sample tasks? Memory effects in the testing of taste discrimination

In order to provide insights into why discrimination protocols with three stimuli sometimes tend to be less sensitive than protocols with two stimuli, two experiments were conducted. In these experiments, the relative effects of memory decay and memory interference were investigated. Both experiments involved purified water and/or solutions of low NaCl concentration. In Experiment 1, three protocols were compared: the traditional same-different test (Protocol 1), the same protocol with a rinse between the two samples (Protocol 2), and Protocol 2 with an added time delay between the first sample and the intermediate rinse (Protocol 3.) The decrease in measured d' values as time delay increased indicated that memory decay might be a factor for tests with three stimuli, such as the triangle method, rendering it less sensitive than tests with two stimuli, such as the same-different method. In Experiment 2, four protocols were compared: the traditional same-different test, the two-rinse same-different test, the triangle test, and what will be called duo same-different test. The experimental design allowed the individual consideration of memory decay and interference effects. From this last experiment, the substantial effect of memory interference was uncovered. Further experimentation will be necessary to estimate the exact relative effects of memory interference and memory decay.     

Influence of item identification on the memory performance of mentally retarded and nonretarded adults

The role of item identification in the memory performance of mentally retarded and nonretarded adults was examined by varying the identification and memory parameters of a sequential same-different task. In Study 1, retarded subjects' identification ability was demonstrated to be less efficient than nonretarded subjects' ability. In Study 2, target duration and interstimulus interval were varied. Memory performance differed between groups, and the memory deficit for retarded subjects was demonstrated to be independent of their identification deficit. The target durations in Study 2 were relatively brief, and in Study 3, the target duration was increased to insure that all subjects could identify the target. Mentally retarded subjects were demonstrated to have a memory deficit. The results were discussed in terms of possible sources of the memory deficit.     

Melody recognition at fast and slow tempos: effects of age, experience, and familiarity

Eighty-one listeners defined by three age ranges (18-30, 31-59, and over 60 years) and three levels of musical experience performed an immediate recognition task requiring the detection of alterations in melodies. On each trial, a brief melody was presented, followed 5 sec later by a test stimulus that either was identical to the target or had two pitches changed, for a same-different judgment. Each melody pair was presented at 0.6 note/sec, 3.0 notes/sec, or 6.0 notes/sec. Performance was better with familiar melodies than with unfamiliar melodies. Overall performance declined slightly with age and improved substantially with increasing experience, in agreement with earlier results in an identification task. Tempo affected performance on familiar tunes (moderate was best), but not on unfamiliar tunes. We discuss these results in terms of theories of dynamic attending, cognitive slowing, and working memory in aging.     

Strategic hand use preferences and hemispheric specialization in tactual reading: impact of the demands of perceptual encoding

Four reading-related, information-processing tasks were administered to right-handed blind readers of braille who differed in level of reading skill and in preference for using the right hand or the left hand when required to read text with just one hand. The tasks were letter identification, same-different matching of letters that differed in tactual similarity, short-term memory for lists of words that varied in tactual and phonological similarity, and paragraph reading with and without a concurrent memory load of digits. The results showed interactions between hand preference and the hand that was actually used to read the stimulus materials, such that left preferrers were significantly faster and more accurate with their left hands than with their right hands whereas right preferrers were slightly but usually not significantly faster with their right hands than with their left hands. In all cases, the absolute magnitude of the left-hand advantage among left preferrers was substantially larger than the right-hand advantage among right preferrers. The results suggest that encoding strategies for dealing with braille are reflected in hand preference and that such strategies operate to modify an underlying but somewhat plastic superiority of the right hemisphere for dealing with the perceptual requirements of tactual reading. These requirements are not the same as those of visual reading, leading to some differences in patterns of hemispheric specialization between readers of braille and readers of print.     

The Eriksen flanker effect revisited.

Four studies are reported on the potential role of perceptual interference in a standard Eriksen flanker task. In the first study, incongruent flanker letters showed the usual effect on choice reaction time (CRT) to the target letter but had no effect on the visual fixation time (VFT) needed to distinguish target and flankers. In the second experiment, the effect of incongruent flankers was studied in the context of a same-different response in regard to the target letter and a subsequently presented single letter. The effect of incongruent flankers vanished at an interstimulus interval of 200 ms. In Experiment 3, the same-different task was used in the paradigm of the functional visual field with a target-flankers combination as stimulus on the left (SL) and a single letter as stimulus on the right side (SR) of the visual field. Flankers did neither affect VFT nor the same-different CRT suggesting that target selection may proceed during the saccade from SL to SR. In Experiment 4 effects were studied of flanker-to-target and target-to-single-letter similarity. Flanker-to-target similarity did neither affect VFT nor same-different CRT but target-to-single-letter similarity prolonged same-different CRT. Together, the results suggest parallel perceptual processing of target and flankers, followed by competition of responses to the target and to the incongruent flankers. In line with earlier research, processes of response selection and response competition appear not to be tied to VFT but to proceed in parallel with the saccade from SL to SR.     

Release of inattentional blindness by high working memory load: elucidating the relationship between working memory and selective attention

An unexpected stimulus often remains unnoticed if attention is focused elsewhere. This inattentional blindness has been shown to be increased under conditions of high memory load. Here we show that increasing working memory load can also have the opposite effect of reducing inattentional blindness (i.e., improving stimulus detection) if stimulus detection is competing for attention with a concurrent visual task. Participants were required to judge which of two lines was the longer while holding in working memory either one digit (low load) or six digits (high load). An unexpected visual stimulus was presented once alongside the line judgment task. Detection of the unexpected stimulus was significantly improved under conditions of higher working memory load. This improvement in performance prompts the striking conclusion that an effect of cognitive load is to increase attentional spread, thereby enhancing our ability to detect perceptual stimuli to which we would normally be inattentionally blind under less taxing cognitive conditions. We discuss the implications of these findings for our understanding of the relationship between working memory and selective attention.     

Dividing attention within and between hemispheres: testing a multiple resources approach to limited-capacity information processing

Two experiments tested the limiting case of a multiple resources approach to resource allocation in information processing. In this framework, the left and right hemispheres are assumed to have separate, limited-capacity pools of undifferentiated resources that are not mutually accessible, so that tasks can overlap in their demand for these resources either completely, partially, or not at all. We tested all three degrees of overlap in demand for left hemisphere supplies, using dual-task methodology in which subjects were induced to pay different amounts of attention to each task. Experiment 1 compared complete and partial overlap by combining a verbal memory load with a task in which subjects named nonsense syllables briefly presented to either the left or right visual field (LVF and RVF, respectively). Experiment 2 compared complete versus no overlap by using the same verbal memory load combined with a laterally presented same-different judgment task that did not require a spoken response. Decrements from single-task performance were always more severe when the visual field task stimulus was presented to the RVF. Further, subjects in Experiment 1 were able to trade performance between tasks on both LVF and RVF trials because there was always at least some overlap in left hemisphere demand. In Experiment 2, performance trade-offs were observed on RVF (complete overlap) trials, but not on LVF trials, where no overlap in demand existed. These results contradict a single-capacity model, but they support the idea that the hemispheres' resource supplies are independent and have implications for both cerebral specialization and divided attention issues.     

Modality differences in short-term memory for rhythms

Prior research has established that performance in short-term memory tasks using auditory rhythmic stimuli is frequently superior to that in tasks using visual stimuli. In five experiments, the reasons for this were explored further. In a same-different task, pairs of brief rhythms were presented in which each rhythm was visual or auditory, resulting in two same-modality conditions and two cross-modality conditions. Three different rates of presentation were used. The results supported the temporal advantage of the auditory modality in short-term memory, which was quite robust at the quickest presentation rates. This advantage tended to decay as the presentation rate was slowed down, consistent with the view that, with time, the temporal patterns were being recoded into a more generic form.     

Reference frames for orientation anisotropies in face recognition and biological-motion perception

Both face recognition and biological-motion perception are strongly orientation-dependent. Recognition performance decreases if the stimuli are rotated with respect to their normal upright orientation. Here, the question whether this effect operates in egocentric coordinates or in environmental coordinates is examined. In addition to the use of rotated stimuli the observers were also rotated and tested both with a same-different face-recognition task and with a biological-motion detection task. A strong orientation effect was found that depended only on the stimulus orientation relative to the observer. This result clearly indicates that orientation effects in both stimulus domains operate in an egocentric frame of reference. This finding is discussed in terms of the particular requirement of extracting sophisticated information for social recognition and communication from faces and biological motion.     

Multidimensional same--different judgments: evidence against independent comparisons of dimensions

Commonly discussed models of performance in the multidimensional same-different task are based on the assumption that independent same-different decisions are reached for each of the stimulus dimensions used in an experiment. In these models, a higher level mechanism examines th outcome of these independent decisions in order to determine whether the stimuli are the same or different overall. Previous evidence indicating that these models are inconsistent with results from same trials is summarized, and a new test of the above assumption using data from different trials is proposed. Detailed analysis of reaction times from different trials is shown, at least for some pairs of dimensions, to be incompatible with the view that separate same-different decisions are reached for each dimension. The major finding is that there are more relatively fast responses in a condition with two dimensions different, compared with the two conditions with only one of the dimensions different, than any processing model treating the dimensions separately could predict. The results suggest that partial information may be combined across dimensions in order to reach a "different" judgment.     

Hemispheric memory for random forms revisited

Hemispheric short-term memory was studied by projecting complex random forms that varied in their verbal association strength to the left and right hemispheres. Male and female subjects responded same or different to a centrally presented memory test stimulus which occurred 0, 5, 10, or 20 sec after the target item. Reaction time for both response judgments was significantly shorter for right-hemisphere presentations over all memory intervals. For both performance measures, response judgment interacted with the length of memory interval and the verbal association value of the stimulus items. No hemispheric differences were observed as a function of subject sex. Hemispheric memory for complex forms appears primarily dependent upon task processing demands rather than stimulus factors when response time is used to measure recognition under tightly controlled conditions.     

Mental size scaling examined

Observers made same-different shape judgments of stimuli that were identical in shape and size different in shape but not in size, or differed in relative size along a number of steps for both same- and different- shaped forms. "Same" judgment RTs increased monotonically with increases in the magnitude of the relative size difference. In contrast, "different" judgment RTs were unaffected by changes in relative size. A second experiment in which stimulus presentation was successive rather than simultaneous yielded essentially the same results. Consideration was given to a dual- process model in which a time-consuming analog process normalizes stimuli that are size discrepant prior to a comparison stage that is operative for those structures responsible for "same" decisions but not for "different" judgments. Some evidence that seems inconsistent with a normalization process which operates prior to contact with memory was discussed, and an alternative explanation in which the early detection of a size difference causes changes in decision criteria was suggested.     

异同判断中“快同效应”的大脑机制：一项ERP研究

采用高密度的事件相关电位（ERPs）技术,记录分析了大学生被试在执行异同判断任务[包括不同颜色刺激对（DC）,不同形状刺激对（DS）和相同刺激对（Same）]时的脑内时程动态变化。行为结果表明,“同”反应的确显著快于“异”反应,表现出明显的快同效应。ERP结果显示：在280-320 ms内,DS和DC条件均比Same条件诱发一个更负的N2成分。偶极子溯源分析表明,DC和DS条件下,N2可能起源于大脑的前扣带皮层（ACC）,可能与“异”反应早期不一致信息（颜色或形状）的认知监控和调节有关;反之Same条件下,N2成分可能起源于楔前叶,主要反映了“同”反应早期知觉识别中整体特征比较加工的过程（同一性指示器）。另外,在450 ms左右, DC和DS比Same条件均诱发了一个更负的P3成分,可能反映了对刺激局部特征的比较和识别（慢速比较器）,并与选择性注意和资源分配等高级认知活动有关;并且,Same条件下P3成分的潜伏期更短,与行为结果一致。以上研究结果表明,异同判断中“同”反应和“异”反应可能有着不同的比较通道和大脑机制,支持双过程模型理论;同时表明,慢速比较器和同一性指示器可能是序列加工的。     

感觉记忆中含语义对象的视觉表征

感觉记忆能够以特征形式构建对视觉对象表面信息的表征, 然而对于具有重要意义的潜在抽象信息, 尚未有研究考察其是否影响感觉记忆的视觉表征。结合掩蔽技术与部分报告法范式考察了感觉记忆的视觉表征中是否包含语义信息。以阿拉伯数字作为目标, 实验1与实验2分别采用正立与倒置的汉字大写数字作为掩蔽刺激, 比较其与白噪音刺激的掩蔽效应。结果显示, 汉字大写数字的掩蔽效应均强于白噪音刺激, 且正立汉字大写数字的掩蔽效果较倒置汉字大写数字更强。实验3采用汉字大写数字与汉字常用字分别作为掩蔽刺激, 结果显示汉字大写数字的掩蔽效果强于汉字常用字。上述结果显示, 刺激间的语义相似性带来了视觉表征冲突, 表明感觉记忆的视觉表征中包含了刺激的语义信息。     

Individual differences in visual comparison processes

Two experiments are reported in which subjects compared the shape of two successively presented random visual forms. The first stimulus in the pair was one of five “standard” shapes, and the second stimulus was either the same as the standard or different by virtue of a perturbation in shape or an overall reflection. Marked individual differences were found in reaction time for the same-different comparison. For one type of subject “same” responses were faster than “different” responses, speed of “different” responses was unaffected by similarity of the test shape to the standard, and error rates and reaction times were not systematically related. For the other type of subject, “different” responses were generally faster than “same” responses, “different” reaction time decreased as the standard shape and the test shape became increasingly dissimilar, and error rates and reaction times were positively correlated. Implications of these individual differences for models of the same-different comparison process are discussed.     

Using selective interference to investigate spatial memory representations

Two experiments used a selective interference procedure in an attempt to determine whether nonverbal visual stimuli were represented in memory in a verbal or spatial format. A spatial representation was clearly implicated. In both experiments, Ss were required to remember either the positions or the identities of seven target items in a 25-item array. During the retention interval for that information, Ss attempted to recognize schematic face or airplane photograph stimuli in a same-different memory task. Memory performance on one or both tasks was greatly impaired when the recall task involved position or spatial information, but was either much less or not at all affected by an identity or verbal information recall task. Because of the selective nature of the interference and on the basis of certain correlational evidence, the experimental results were also interpreted as providing support for the notion that verbal and spatial information are stored and processed in separate information-processing systems.