Why are artificial polymorphous concepts so hard for birds to learn?

Stimulus sets defined in terms of artificial polymorphous concepts have frequently been used in experiments to investigate the mechanisms of discrimination of natural concepts, both in humans and in other animals. However, such stimulus sets are frequently difficult for either animals or humans to discriminate. Properties of artificial polymorphous stimulus sets that might explain this difficulty include the complexity of the individual stimuli, the unreliable reinforcement of individual positive features, attentional load, difficulties in discriminating some stimulus dimensions, memory load, and a lack of the correlation between features that characterizes natural concepts. An experiment using chickens as subjects and complex artificial visual stimulus sets investigated these hypotheses by training the birds in discriminations that were not polymorphous but did have some of the properties listed above. Discriminations that involved unreliable reinforcement or high attentional load were found to approach the difficulty of polymorphous concept discriminations, and these two factors together were sufficient to account for the entire difficulty. The usual kind of artificial polymorphous concept may not be a good model for natural concepts as they are perceived and discriminated by birds. A RULEX account of natural concept learning may be preferable.     

Why are artificial polymorphous concepts so hard for birds to learn?

Stimulus sets defined in terms of artificial polymorphous concepts have frequently been used in experiments to investigate the mechanisms of discrimination of natural concepts, both in humans and in other animals. However, such stimulus sets are frequently difficult for either animals or humans to discriminate. Properties of artificial polymorphous stimulus sets that might explain this difficulty include the complexity of the individual stimuli, the unreliable reinforcement of individual positive features, attentional load, difficulties in discriminating some stimulus dimensions, memory load, and a lack of the correlation between features that characterizes natural concepts. An experiment using chickens as subjects and complex artificial visual stimulus sets investigated these hypotheses by training the birds in discriminations that were not polymorphous but did have some of the properties listed above. Discriminations that involved unreliable reinforcement or high attentional load were found to approach the difficulty of polymorphous concept discriminations, and these two factors together were sufficient to account for the entire difficulty. The usual kind of artificial polymorphous concept may not be a good model for natural concepts as they are perceived and discriminated by birds. A RULEX account of natural concept learning may be preferable.     

Effect of list length on recall after dichotomous visual presentation

A visual analogue of an auditory dichotic listening experiment was carried out using what may be termed dichotomous visual presentation of lists of either three or four stimuli. Each stimulus consisted of several identical letters which were arranged so as to form the outline of a second, large letter. Subjects attended to either the small or large letters, and recalled either the attended or unattended letters first. It was found that the results for the three-stimulus and four-stimulus lists differed substantially; they were interpreted as consistent with the model of short-term memory proposed by Broadbent (1975).     

Iconic memory and visible persistence

There are three senses in which a visual stimulus may be said to persist psychologically for some time after its physical offset. First, neural activity in the visual system evoked by the stimulus may continue after stimulus offset (“neural persistence”). Second, the stimulus may continue to be visible for some time after its offset (“visible persistence”). Finally, information about visual properties of the stimulus may continue to be available to an observer for some time after stimulus offset (“informational persistence”). These three forms of visual persistence are widely assumed to reflect a single underlying process: a decaying visual trace that (1) consists of afteractivity in the visual system, (2) is visible, and (3) is the source of visual information in experiments on decaying visual memory. It is argued here that this assumption is incorrect. Studies of visible persistence are reviewed; seven different techniques that have been used for investigating visible persistence are identified, and it is pointed out that numerous studies using a variety of techniques have demonstrated two fundamental properties of visible persistence: theinverse duration effect (the longer a stimulus lasts, the shorter is its persistence after stimulus offset) and theinverse intensity effect (the more intense the stimulus, the briefer its persistence). Only when stimuli are so intense as to produce afterimages do these two effects fail to occur. Work on neural persistences is briefly reviewed; such persistences exist at the photoreceptor level and at various stages in the visual pathways. It is proposed that visible persistence depends upon both of these types of neural persistence; furthermore, there must be an additional neural locus, since a purely stereoscopic (and hence cortical) form of visible persistence exists. It is argued that informational persistence is defined by the use of the partial report methods introduced by Averbach and Coriell (1961) and Sperling (1960), and the term “iconic memory” is used to describe this form of persistence. Several studies of the effects of stimulus duration and stimulus intensity upon the duration of iconic memory have been carried out. Their results demonstrate that the duration of iconic memory is not inversely related to stimulus duration or stimulus intensity. It follows that informational persistence or iconic memory cannot be identified with visible persistence, since they have fundamentally different properties. One implication of this claim that one cannot investigate iconic memory by tasks that require the subject to make phenomenological judgments about the duration of a visual display. In other words, the so-called “direct methods” for studying iconic memory do not provide information about iconic memory. Another implication is that iconic memory is not intimately tied to processes going on in the visual system (as visible persistence is); provided a stimulus is adequately legible, its physical parameters have little influence upon its iconic memory. The paper concludes by pointing out that there exists an alternative to the usual view of iconic memory as a precategorical sensory buffer. According to this alternative, iconic memory is post-categorical, occurring subsequent to stimulus identification. Here, stimulus identification is considered to be a rapid automatic process which does not require buffer storage, but which provides no information about episodic properties of a visual stimulus. Information about these physical stimulus properties must, in some way, be temporarily attached to a representation of the stimulus in semantic memory; and it is this temporarily attached physical information which constitutes iconic memory.     

The effects of a task-irrelevant visual event on spatial working memory

In the present experiment, we investigated whether the memory of a location is affected by the occurrence of an irrelevant visual event. Participants had to memorize the location of a dot. During the retention interval, a task-irrelevant stimulus was presented with abrupt onset somewhere in the visual field. Results showed that the spatial memory representation was affected by the occurrence of the external irrelevant event relative to a control condition in which there was no external event. Specifically, the memorized location was shifted toward the location of the task-irrelevant stimulus. This effect was only present when the onset was close in space to the memory representation. These findings suggest that the “internal” spatial map used for keeping a location in spatial working memory and the “external” spatial map that is affected by exogenous events in the outside world are either the same or tightly linked.     

Rehearsal,generative processes,and the activation of underlying stimulus representations

Previous research found that subjects engaged in mental rehearsal could reduce stimulus encoding time in classification and identification tasks by generating an appropriate representation of the probe stimulus prior to its presentation. The present experiment examined the types of representational codes activated by generative processes in character classification. Numerical stimuli were employed which could differ visually, yet have the same name and meaning (e.g., TWO, 2, II, &.). The results indicate that generative processes may activate visual and nonvisual memory codes prior to the encoding of an external stimulus. Effects of generative processes were discussed in terms of an activation model which defines the function of rehearsal in perceptual processing. Attention, through rehearsal, activates stimulus representations which are described by distributions of activation which change continuously over time. The momentary state of each distribution determines the rate of stimulus encoding.     

反馈延迟对信息整合类别学习的影响：视觉项目精准性的调节作用

研究旨在探究更精确的视觉项目表征能否消除延迟反馈对信息整合学习的损害。实验采用2（视觉项目表征精确性：精确/非精确）×2（反馈延迟：即时反馈/延迟反馈）组间设计,结果发现无论有无延迟反馈,精确的项目表征条件下类别学习成绩都显著高于非精确条件,精确性与反馈延迟存在交互作用。采用状态痕迹分析进一步证明精确性显著影响信息整合类别学习的稳定性。在反馈延迟条件下,精确的视觉项目表征能提高信息整合类别学习的成绩。     

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。     

Generation of visual representations

The visual confusability of uppercase letters was manipulated in a successive same-different task to study the conditions under which visual generation from auditory inputs would occur and to investigate the figural specificity of the generated representations. Prior experiments have shown that visual confusions do occur when the initial stimulus is auditory and the second one is visual, which indicates that auditory stimuli can be encoded into visual forms. There has been some suggestion, however, that the generated visual code may have been too abstract to differentiate between the two cases in which letters can appear. In the present experiment, although the confusion effect was not eliminated when the subjects had no advance knowledge regarding the case in which the visual stimulus would appear, the marked confusion effect obtained when the visual stimulus was an uppercase letter was substantially attenuated when the letter appeared in lowercase. This was taken to indicate that the visual characteristics of a generated visual representation may be relatively specific. The results also suggested that subjects may wait until after the second stimulus is presented before they generate the visual representation of the initial auditory stimulus.     

Visual attribute modulates the time course of iconic memory decay

Studies on iconic memory demonstrate that rich information from a visual scene quickly becomes unavailable with the passage of time. The decay rate of iconic memory refers to the dynamics of memory availability. The present study investigated the iconic memory decay of different stimulus attributes that comprised an object. Specifically, in Experiment 1, participants were presented with eight coloured numbers (e.g., red 4) and required to remember only one attribute, either colour or number, over different blocks of trials. The participants then reported the cued attribute in which the cue Stimulus Onset Asynchrony (SOA) from the memory array onset was varied (0, 100, 200, 300, 500, and 1000?ms). We found that numerical information became unavailable more quickly than colour information, despite the fact that the memory accuracies at 0 and 1000?ms SOAs were comparable between the two attributes. In Experiment 2, we replicated the finding that a numerical representation was lost more quickly than a colour representation when visual masks followed the target stimulus. These results suggest that the various visual attributes comprising an object are lost over time at different rates in iconic memory. We discuss this finding in relation to how perceptual representation is transferred to the capacity-limited visual working memory.     

The representation of color and form in long-term memory

Color and form are elementary stimulus encoding dimensions that have effects on the representation of visual stimuli at early processing stages. Little is known, however, about their effects on visual long-term memory. In three experiments we investigated whether color is part of the memory representation, whether color and form are bound in the memory representation, and the effect of color context on memory performance. Experimental results suggest that color is part of the memory representation and that color and form can be represented separately in memory and accessed independently. We suggest that the binding of color and form is a deliberate strategic act that requires focal attention, not a natural consequence of processing visual stimuli. We compare our results with the predictions of two computational memory models regarding feature binding. The effect of color context was not straightforward; however, results are consistent with the encoding specificity principle.     

Parallel scanning of auditory and visual information

Two experiments involving memory retrieval of auditorilv and visually presented materials were performed. In Experiment I, subjects were presented with memory sets of 1, 2, or 4 stimuli and then with a test item to be classified as belonging or not belonging to the memory set. In Condition 1, each memory stimulus was a single, auditorily presented letter. In Condition 2, each memory stimulus was a visually presented letter. In Conditions 3 and 4, each memory stimulus was a pair of letters, one presented visually and the other auditorily. Mean reaction time (RT) for the classification task increased as a function of number of memory stimuli at equal rates for all four conditions. This was interpreted as evidence for a parallel scanning process in Conditions 3 and 4 where the auditory item and visual item of each memory stimulus pair can be scanned simultaneously. Experiment II compared memory retrieval for a simultaneous condition in which auditory and visual memory items were presented as pairs with a sequential condition in which mixed auditory-visual memory sets were presented one item at a time. RTs were shorter for the simultaneous condition. This was interpreted as evidence that parallel scanning may depend upon memory input parameters.     

无关长时记忆表征能否引导视觉注意选择?

与任务相关的长时记忆表征在引导视觉注意选择的过程中扮演着重要的角色,它可以使人们在熟悉的视觉情境中快速搜索目标刺激,并偏离干扰刺激。但当长时记忆表征与任务无关时,还能否引导视觉注意选择?目前还不清楚。实验1采用眼动追踪技术直接比较无关工作记忆表征与无关长时记忆表征在视觉搜索阶段对视觉注意的捕获效应,行为反应时与首次注视点百分率的结果都发现,当无关工作记忆表征在视觉搜索中再次出现时能引导视觉注意偏向到与之匹配的干扰刺激,但无关长时记忆表征并没有表现出类似的注意引导效应;实验2探讨记忆表征由工作记忆系统转移到长时记忆系统的过程中对视觉注意的引导效应,结果发现,随着记忆表征的转移,注意引导效应消失了,实验3排除工作记忆表征的干扰后,依然没有发现无关长时记忆表征对注意的引导效应。以上结果表明,无关长时记忆表征并不能像工作记忆表征一样引导视觉注意选择,工作记忆表征和长时记忆表征对视觉注意的引导属于两个不同的认知过程。     

不同编码对听写困难儿童字形记忆的促进效应

听写困难是一种发生率较高的儿童学习障碍现象。实验考察笔画语音编码和动作编码对听写困难儿童字形记忆水平的影响。结果发现, 笔画语音编码对听写困难儿童的字形记忆成绩没有明显影响, 但却明显促进了正常儿童的字形记忆成绩; 与之相对, 动作编码对正常儿童的字形记忆成绩没有明显影响, 但却明显促进了听写困难儿童的字形记忆成绩。上述现象, 既可能源于编码加工阶段, 也可能源于字形表征的提取阶段。     

Spatial relational memory in 9-month-old macaque monkeys

This experiment assesses spatial and nonspatial relational memory in freely moving 9-mo-old and adult (11-13-yr-old) macaque monkeys (Macaca mulatta). We tested the use of proximal landmarks, two different objects placed at the center of an open-field arena, as conditional cues allowing monkeys to predict the location of food rewards hidden in one of two sets of three distinct locations. Monkeys were tested in two different conditions: (1) when local visual cues marked the two sets of potentially baited locations, so that monkeys could use both local and spatial information to discriminate these locations from never-baited locations; and (2) when no local visual cues marked the two sets of potentially baited locations, so that monkeys had to rely on a spatial relational representation of the environment to discriminate these locations. No 9-mo-old or adult monkey associated the presence of the proximal landmarks, at the center of the arena, with the presence of food in one set of three distinct locations. All monkeys, however, discriminated the potentially baited locations in the presence of local visual cues, thus providing evidence of visual discrimination learning. More importantly, all 9-mo-old monkeys tested discriminated the potentially baited locations in absence of the local visual cues, thus exhibiting evidence of spatial relational learning. These findings indicate that spatial memory processes characterized by a relational representation of the environment are present as early as 9 mo of age in macaque monkeys.     

Effects of temporal asynchrony and stimulus magnitude on competitive audio–visual binding

When making decisions as to whether or not to bind auditory and visual information, temporal and stimulus factors both contribute to the presumption of multimodal unity. In order to study the interaction between these factors, we conducted an experiment in which auditory and visual stimuli were placed in competitive binding scenarios, whereby an auditory stimulus was assigned to either a primary or a secondary anchor in a visual context (VAV) or a visual stimulus was assigned to either a primary or secondary anchor in an auditory context (AVA). Temporal factors were manipulated by varying the onset of the to-be-bound stimulus in relation to the two anchors. Stimulus factors were manipulated by varying the magnitudes of the visual (size) and auditory (intensity) signals. The results supported the dominance of temporal factors in auditory contexts, in that effects of time were stronger in AVA than in VAV contexts, and stimulus factors in visual contexts, in that effects of magnitude were stronger in VAV than in AVA contexts. These findings indicate the precedence for temporal factors, with particular reliance on stimulus factors when the to-be-assigned stimulus was temporally ambiguous. Stimulus factors seem to be driven by high-magnitude presentation rather than cross-modal congruency. The interactions between temporal and stimulus factors, modality weighting, discriminability, and object representation highlight some of the factors that contribute to audio–visual binding.     

Secobarbital and perceptual processing

An experiment which employed each of 18 subjects in four days of testing was used to examine acute secobarbital dose treatment effects on choice reaction time in a Cooper and Shepard (1973) character recognition task. Manipulations of visual stimulus degradation, character difficulty, 180 degree rotation, and mirror-image reversal were included in order to evaluate the hypothesis that the drug affects performance by disrupting early stimulus input processing. The results indicate significant increases in the effect of secobarbital on reaction time and errors under conditions of visual stimulus degradation. The effects of the drug, however, were not changed by 180 degree rotation of the target character or by the other task variables. The results were interpreted to indicate that secobarbital impairs performance primarily by placing selective stress on hypothetical early encoding activities and that later processing operations (associated with use of an internal representation of the target character) are not affected by the drug. Strengths and weaknesses of the two-stage model of visual stimulus processing are discussed and implications of the model for future drug research are indicated.     

工作记忆表征的激活与抑制状态对注意引导效应的影响

本研究采用双任务范式, 通过定向遗忘任务操纵工作记忆表征状态, 分别在目标无关和目标相关条件下考察工作记忆激活与抑制状态对视觉搜索早期注意引导效应的影响。实验1与实验2发现当工作记忆表征只可能与视觉搜索分心物匹配时(目标无关条件), 处于激活状态的工作记忆表征会引导视觉注意偏向到与之匹配的分心物, 表现出注意引导效应, 而处于抑制状态的工作记忆表征则没有观察到注意引导效应。实验3与实验4发现, 当工作记忆表征有可能与视觉搜索目标匹配时(目标相关条件), 处于激活状态的工作记忆表征能捕获注意, 而处于抑制状态的工作记忆表征只有与视觉搜索目标匹配时, 才表现出对该搜索目标反应的延迟。这些研究的结果表明(1)处于激活状态的工作记忆表征能有效地引导注意偏向到与之匹配的搜索目标或分心物, 并且这种注意引导效应并未受到抑制动机的影响而被消除或反转; (2)处于抑制状态的工作记忆表征能将抑制状态传递到视觉搜索阶段, 并延迟对与之匹配的搜索目标的反应。     

Visual memory performance for color depends on spatiotemporal context

Performance on visual short-term memory for features has been known to depend on stimulus complexity, spatial layout, and feature context. However, with few exceptions, memory capacity has been measured for abruptly appearing, single-instance displays. In everyday life, objects often have a spatiotemporal history as they or the observer move around. In three experiments, we investigated the effect of spatiotemporal history on explicit memory for color. Observers saw a memory display emerge from behind a wall, after which it disappeared again. The test display then emerged from either the same side as the memory display or the opposite side. In the first two experiments, memory improved for intermediate set sizes when the test display emerged in the same way as the memory display. A third experiment then showed that the benefit was tied to the original motion trajectory and not to the display object per se. The results indicate that memory for color is embedded in a richer episodic context that includes the spatiotemporal history of the display.