心理科学进展 2011, Vol. 19, No. 6, 775–793 Advances in Psychological Science DOI: 10.3724/SP.J.1042.2011.00775 ·主编特邀(Editor-In-Chief Invited)· 编者按: 科学赋予心理学的一项重大任务是去揭开人类意识之谜。随着心理学实验技术和认知神经科学手段 的不断发展, 人们似乎已经开始接近其中的某些核心问题, 如前意识现象, 如认知过程与脑神经过程的 交互作用等。笛卡尔的身心二元论将不仅继续受到思辨的挑战, 更要受到实证研究的挑战。 Ernst Pöppel 等人的“‘时间窗’—— 认知加工的后勤基础”一文, 以德国人所具有的欧洲大陆哲学的 视角, 提出了认知神经系统的“时间窗”概念, 并系统介绍了有关时间窗与认知加工的实证研究。时间窗 是大脑在进化过程中发展出来的减少复杂性和时间不确定性的特殊机制, 正是在刺激所触发的神经震 荡的窗口期, 神经系统可以控制和减低时间的不确定性和噪音。时间窗概念使人们可以将神经基础如何 作用的机制与意识表征的内容之间作出区分。来自视觉、听觉、触觉通道研究的证据, 来自单细胞和群 组细胞的研究证据, 以及来自于传统反应时和时间知觉阈研究的证据, 都支持有关时间窗的理论思考。 文本还着重介绍了 20~60 毫秒范围的“时间窗”、2~3 秒范围的“时间窗”、以及人类日常生活中所熟 悉的 24 小时的“时间窗”, 并呈现给读者三种时间窗的研究对于回答基本科学问题、以及对于解决人类 现实生活中的实际问题的重大意义。 本刊编辑部特邀请 Ernst Pöppel 及其合作者为本刊撰写此文, Ernst Pöppel 教授欣然接受了邀请, 并 很快成文寄送给我们。在此我们对他表示十分感谢。我们希望通过此文的发表, 能够启发我国心理学工 作者的思路, 促进心理学研究更深入和更广泛的创新。 (本文责任编辑:张建新) “Temporal Windows” as Logistical Basis for Cognitive Processing Ernst Pöppel1,2, Yan BAO1,2, Bin ZHOU1,3 1 ( Institute of Medical Psychology and Human Science Center, University of Munich, Germany) 2 ( Department of Psychology and Key Laboratory of Machine Perception (Ministry of Education), Peking University, Beijing 100871, China) (3 Institute of Psychology, Chinese Academy of Sciences, Beijing 100101, China) Abstract: Temporal processing is an intrinsic feature of cognitive processing. Thus, it is important to have an understanding about temporal processing in perception or cognition in general. To overcome some extrinsic challenges in central information processing, the brain has apparently developed special temporal windows within which information is integrated. One such window has been found in the range of some tens of milliseconds, and it serves to create the necessary building blocks for conscious activity. Empirical evidence comes from studies on reaction time, temporal order threshold or oscillatory responses in neuronal structures. Another temporal window operates in the range of two to three seconds and it serves to create the “subjective presence”, or temporal integration intervals within which the identity of percepts is maintained. Empirical evidence comes from studies on the reproduction of time intervals, ambiguous figures, sensorimotor synchronization or neurophysiological research. Another kind of temporal window is given with the diurnal rhythms; all psychological or physiological functions show apparently a 24-hour variability. Received date: 2011-03-07 Correspondence to: Dr. Yan Bao, E-mail: [email protected] 775 776 第 19 卷 心 理 科 学 进 展 Disturbances in temporal windows may show up in neurological or psychiatric diseases indicating the importance of studies in temporal processing beyond basic research. Key words: temporal perception, order threshold, reaction time, neuronal oscillation, circadian rhythm 1 Temporal Processing from a Historical Perspective When psychology defined itself some 150 years ago (Fechner, 1860), “time” was a central topic. Important questions with respect to time estimation or temporal perception have been formulated already in the sixties of the nineteenth century. And in a textbook published 100 years ago, Wilhelm Wundt, who started the first laboratory in experimental psychology, summarized already important results. What were such early insights into how we deal with time, what questions were attacked at the beginning of scientific psychology? It was for instance the Baltic biologist Karl Ernst von Baer (1865) who came up with a notion of the interested in the discrimination of different temporal durations, and in studying differential sensitivity in the auditory modality, he observed that there is no experience of duration for intervals that are shorter than 40 milliseconds using technology that already then was available; such durations can be said to be experienced as “points in time” - but physically speaking they have a duration. On the basis of this observation one can interpret such a time point as a representation of the moment for humans as hypothesized by Karl Ernst von Baer. The time point with a finite duration can also be looked at as a “temporal window” within which “primordial events” are constructed which are the building blocks for our conscious activity (see below and Pöppel, 1994, 1997, 2009). moment, i.e. the longest possible time interval to be Today, one and a half centuries after the first objectively measured without apparent duration. experimental Von Baer pointed out that different organisms perception, probably every psychological laboratory because of a different organization of their sense uses measurements of reaction time as a paradigm organs and their brains presumably have different to look into the complexity and dynamics of moments if measured with external means, namely cognitive processing. Chronometric analyses have with clocks. This concept of a moment has become important indicators for brain processes and important consequences for an understanding of cognitive activities. This experimental paradigm psychological processes; it implies that we step out goes back to the Dutch scientist Karl Donders of the continuous flow of time as described by Isaac (1868), who used simple and choice reaction times Newton to get a better understanding for instance of (Philosophiae Mathematica, 1687): Universalis “Absolute, Principia true attempts to understand temporal and decisions. His experiments started perhaps the most mathematical time by itself and from its own nature important success story in experimental psychology flows equably without relation to anything external”. and cognitive neuroscience. It is worth noting, In spite of this early insight we tend to forget its however, that the use of reaction times as indicators implications for a deeper understanding of cognition, for and we usually treat time as a continuous variable, hypothesis that indeed such operations are of i.e. looking at time as a “container” within which sequential cognitive processing is implemented. possibility that mental operations may actually be mental operations nature. This rests on the hypothesis implicit hides the An empirical answer to the question how long parallel (Pöppel and Bao, 2011a), and that the a moment could be for humans was given shortly experimental setup selects from these parallel after the speculation of Karl Ernst von Baer by the operations one activity and shifts it into a frame of Austrian physicist Ernst Mach (1865). He was sequentiality; by doing so the experimenter might 第6期 “Temporal Windows” as Logistical Basis for Cognitive Processing 777 be seduced to conclude that other activities which the construction of such reference points might be have not been selected are in fact non-existent. that stimuli with higher probability should be Whereas Karl Ernst von Baer, Ernst Mach and processed with better differential sensitivity which Karl Donders were looking at rather short temporal is suggested to happen closer to the reference point. intervals being basic for cognitive processing, Karl Such a mechanism of temporal adaptation would Vierorth (1868) from Tübingen in Germany was imply the existence of a special temporal memory interested humans can which is continuously calibrated by stimuli of reproduce the duration of temporal intervals which different durations. Such a mnemonic system might last for several seconds. He observed that short be the basis for temporal impressions of events temporal intervals are reproduced longer than the lasting long or short. in the question how stimulus, and longer intervals are reproduced shorter than the stimulus. This observation implies that between long and short intervals there must be 2 Challenges for Cognitive Processing Caused by Temporal Uncertainties an interval which is reproduced correctly; this interval is usually referred to as “indifference point”. One essential feature of perception or action is The question came up whether such an indifference their effortless availability. We have an effortless point is an experimental artifact, or whether it access to images, words, smells, memories or reflects an underlying neuronal process which movements (Pöppel and Bao, 2011a). When we determines temporal perception (Pöppel, 1971). open our eyes, we see immediately something; Interestingly, both answers are correct. If in an without hesitation we can speak in our mother experiment temporal intervals to be reproduced are tongue and understand the language of others; if we chosen between one second and several seconds smell something, we do not have to think about it; (like seven seconds), one observes an indifference in daily life our memory serves us to recognize our point at approximately three seconds. Furthermore, family members immediately; and walking in a reproductions up to this indifference point show a bipedal way, which really distinguishes us from small variance whereas reproductions beyond this other mammals, happens automatically. Everything point show a sudden increase of variance. The said is, however, only true if our brain is intact, if indifference point at this stimulus duration may our “neuronal machinery” works properly. When reflect a neuronal process of high temporal stability patients have suffered injuries, this effortless being perhaps responsible for pre-semantic temporal processing may no longer be possible. In fact, we integration (Pöppel, 2009). It can, however, also be learn about effortless processing in the normal case, demonstrated regions because it can be lost. Looking at the complexity of indifference points are observed which do not the neuronal representation of information, the easy reflect a temporally stable integration process, but and effortless availability of the basic repertory of which are created by the specific experimental conscious phenomena is difficult to understand. conditions. As has been suggested in the adaptation Apparently the nervous system has developed level theory by Helson (1964) human observers strategies mentally construct a reference point, if they are complexity and in particular of temporal uncertainty. exposed in an experimental setting to stimuli of Where do these problems come from and how are different intensity or different duration. These they solved? There are several sources giving rise to reference points may correspond to the geometric complexity and temporal uncertainty, namely the mean physics and the biophysics of the stimuli and in of all that in stimuli other temporal presented during an experimental situation. The ecological reason for to overcome inherent addition their central representation. problems of 778 第 19 卷 心 理 科 学 进 展 One source of complexity comes from stimulus neuroanatomical studies there is a large degree of transduction which is principally different in divergence in the projection systems (Nauta and different sensory modalities. For instance, the Feirtag, 1986). It has been estimated that each transduction takes less than 1 ms in the auditory central neuron innervates approximately 10,000 system and more than 20 ms in the visual system other neurons. This means that local information is (Pöppel et al., 1990b). Thus, auditory and visual spread out over a broad field of receptive neurons information arrive at different times in central and because of the different transmission times structures. Matters become more complicated by the along the axons, this local information is not only fact that the transduction time in the visual modality distributed spatially but it is also spread out over is flux-dependent, i.e. that surfaces with less flux time leading to temporal uncertainty. Another increase of complexity is provided by require more transduction time at the receptor surface. Thus, to see an object with areas of the mode of different brightness or to see somebody talking, experimental evidence using imaging technology different temporal availabilities of local activities like fMRI, MEG or PET indicates that each within the visual modality and similarly different functional state is characterized by a spatiotemporal local activities across the two modalities engaged in pattern stimulus processing have to be overcome. If in Gutyrchik et al, 2010; Ilg et al., 2007). Different addition somatosensory information has to be modules in the visual modality (being for instance integrated to identify an object, the neuro-cognitive responsible system is confronted with even more temporal recognition) and similarly in the auditory modality challenges of functional modular for representation. activities colour (Pöppel, perception New 1989; or facial the (being for instance responsible for the prosody or somatosensory system again is different compared the semantics of speech) are co-activated. Thus, not to the auditory or visual modality. only on the cellular but also on the modular level as transduction time in For intersensory integration besides these biophysical problems as a consequence of the the brain has to deal with the integration of spatially distributed and temporally ill-defined information. transduction times also physical problems have to How can this high degree of complexity and be considered. The distance of objects to be temporal uncertainty be overcome? In a radically perceived is obviously never predetermined. Thus, cognitive approach (which in an epistemological the speed of sound (not of light) becomes a critical sense would imply dualism with respect to the factor. Approximately at a distance of 10 to 12 mind-body problem) one could argue that there is meter transduction time in the retina under optimal no problem at all; the problems as described above conditions corresponds to the time the sound takes are irrelevant as the amount of temporal noise (up to to arrive at the recipient. Up to this “horizon of some tens of ms) is very small and on the basis of a simultaneity” (Pöppel et al., 1990b) auditory situational analysis the categorical definition of information is earlier than visual information; percepts follows a top-down analysis in which beyond this horizon, visual information arrives problems of sensory input or representational earlier. Again, there must be some kind of specifics become irrelevant. But in advanced mechanism temporal cognitive neuroscience and psychology such a uncertainty of information which is represented in metaphysical attitude appears to be inappropriate. the two sensory modalities. There is “no ghost in the machine” that solves the which overcomes the Besides biophysical and physical challenges problem the brain is confronted with. The there is a further temporal problem introduced by neuro-cognitive system has to solve the problems the specific brain architecture. As has been shown in itself with mechanisms that allow reliable 第6期 “Temporal Windows” as Logistical Basis for Cognitive Processing 779 information processing. The hypothesis suggested to numerical values are obtained, this fact strongly overcome temporal supports the validity of these observations as a basis uncertainty is based on the concept of “temporal for deriving a general principle. One might refer to windows” presumably implemented by oscillatory this activities (Wiener, 1958, Pöppel, 1971; Pöppel et al. “induction” as a mental operation as the “Darwinian 1990a). Principle” as Charles Darwin in his seminal work the complexity and the mode of a scientific conclusion using “The Origin of Species” (1859) equally based his 3 “Temporal Window” for Reduction of Temporal Uncertainty conclusions on many independent observations. An important example supporting the conceptual notion of a temporal window in this time It is argued that the brain has developed domain comes from observations with patients who specific mechanisms to reduce complexity and have to undergo a general anesthesia (Madler and temporal uncertainty. One essential support for this Pöppel, 1987; Schwender et al., 1994). During hypothesis comes from the fact that the same wakefulness, one observes an oscillatory activity temporal is with periods of 30 to 40 ms in the auditory evoked observed in the visual, auditory or tactile modality, potential (Galambos et al., 1981). During anesthesia on the level of single-cell or neuronal group this activities, assemblies value on of the information level processing of cognition, in oscillatory activity disappears within which the neuronal under normal measurements of reaction times or of temporal order circumstances presumably reflects such internal thresholds. It is suggested that temporal noise can system states. The auditory information is still be brought under control if the nervous system uses transduced on the receptive surface as can be stimulus triggered neuronal oscillations. One period concluded from the presence of brain stem of such a “relaxation oscillation” is supposed to potentials, but further processing states appear to be represent the logistical basis for a system state blocked. As a result patients in such a state process within which temporally and spatially distributed no sensory information that might be used for a information can be integrated. These states are conscious representation. Such patients report that “a-temporal” because the before-after relationship other than during sleep no time seems to be have of stimuli processed within such states is not passed between the beginning of the anesthesia and these the reawakening after anesthesia. This oscillatory hypothetical states is observed in the time domain of process which is apparently implemented in the 30 to 60 milliseconds (Pöppel, 1970, 1994, 1997a, cortico-thalamic 2009). Interestingly, the concept of elementary framework for the reduction of temporal uncertainty. integration units has also become fruitful for It can be argued that this process is the neuronal physical theories on time (Ruhnau, 1994), stressing basis for the creation of “primordial events” or the the interdisciplinary nature of research. building blocks of conscious activity. defined. Experimental evidence for pathway provides a formal What is the empirical evidence for “time It is important to note that this temporal windows” within the indicated range of some tens window in its duration is not determined by what is of processed, milliseconds? There are indeed many i.e. the prior content, to any but that content. it is Thus, it experimental observations using different paradigms implemented that such a mechanism must be at work, old and represents an automatic presemantic process to be new (Pöppel, 1978). The reference to “different used for different kinds of information. This issue paradigms” is important: If it can be shown that will come up again later when referring to a using different experimental setups always similar temporal window in the range of a few seconds, and 780 第 19 卷 心 理 科 学 进 展 it is of utmost importance for an understanding of order threshold can also be successfully measured in cognitive processing. One has to distinguish animal models (Wada et al., 2005), indicating the between universality of a temporal window going beyond logistical or “How-Functions” that represent the necessary neuronal infrastructure, and human temporal perception. content or “What-Functions” that become the basis But one should also be aware of the flexibility of conscious representation (Pöppel, 1989, 2010; of temporal order perception in humans. In a recent Pöppel and Bao, 2011b; Pöppel and Ruhnau, 2011). study it could be demonstrated that there is a Strong experimental evidence for a temporal fundamental difference between temporal order window or elementary processing units comes also thresholds for click stimuli and for tone stimuli from research on temporal order threshold (Hirsh (Bao et al., 2011c). Whereas click stimuli with a and Sherrick, 1961; Lotze et al. 1999; Kanabus et al., duration of 1 ms do not indicate any difference 2002; Fink et al., 2006). In such experiments between subjects coming from different speech subjects have to indicate in which temporal order environments, temporal order thresholds for tone stimuli have been presented, like which ear was stimuli of 10 ms duration result in a double stimulated first when both ears are stimulated by dissociation: Chinese subjects have a rather short acoustic signals with a short temporal delay. It has temporal order threshold for tones with near been shown that temporal order threshold has frequencies and a high threshold for tones with far approximately the same value of some tens of frequencies (600 vs 1200 HZ in the first case; 400 milliseconds for the visual, auditory and tactile vs 3000 Hz in the second case), Polish subjects modality. The correspondence of these values in show exactly the reverse pattern. Although temporal spite order threshold for tone stimuli with monaural of qualitatively different transduction processes in the sensory modalities favors the presentation mode is demonstrated to be hypothesis of a common central mechanism for independent of tone frequencies (Fang and Bao, these systems. As the indication of a temporal order 2011), the double dissociation results of tone stimuli requires that events have to be defined in the first with binaural presentation mode suggest a strong place to be brought into a sequence, one can impact of speech experience on temporal order conclude that this mechanism is also necessary to be perception. Presumably Chinese as a tonal language used for the identification of “primordial events” imprints the brain in a selective way to develop a which are the building blocks of conscious activity. higher sensitivity for perceiving the temporal order The usefulness of measuring temporal order of near frequency tones, whereas Polish as a threshold in brain injured patients has been language rich in consonants does it the other way convincingly and around. These studies also indicate that the choice colleagues (2004). In general, it has been shown of an experimental paradigm can be essential for the how useful experimental procedures on temporal conclusions to be derived, and that contradictory processing can be applied for clinical populations results sometime can be the consequence of (Hari and Kiesilä, 1996), although one has to be intervening variables which are outside the focus of aware of the individual differences due to age, attention. demonstrated by Wittmann gender or other factors (Szymaszek et al., 2006, A different domain of research, i.e. the study of 2009; Kolodziejczyk and Szelag, 2008). Recent eye movements, also supports the notion of a experiments tools temporally segmented information processing with support the practicality of measuring temporal order successive steps of approximately 30 to 40 thresholds on the clinical level (Lewandowska et al., milliseconds. If a subject initiates pursuit eye 2008). And it has been demonstrated that temporal movements when a visual target starts to move, the using electrophysiological 第6期 “Temporal Windows” as Logistical Basis for Cognitive Processing 781 latency of these movements shows a multimodal plateau of performance when choice reaction time is distribution of responses with temporal intervals measured which would indicate then stationarity or between the modes of 30 to 40 ms (Pöppel and stable Logothetis, 1986); unimodal response histograms (Steinbach et al., 1991). The answer came as a are usually the consequence of too broad a bin surprise as it takes many thousand trials when a width in measuring the latency; with a bin width of choice has to be made between auditory and visual 20 ms or even more selective response modes with a stimuli presented in random order. This observation temporal separation of 30 to 40 ms are necessarily suggests that most of the experiments done in masked. conditions for systematic observations response cognitive science when response time is used as a histograms can also be seen when saccadic eye variable to get insight into the cognitive machinery movements are measured although their latency is are done under conditions of instationarity as much longer than the one for pursuit eye movements usually only some tens or hundreds of trials are (Frost and Pöppel, 1976). recorded. Such multimodalities in Multimodal response histograms have also In a further experiment additional knowledge been observed for choice reaction time (Pöppel, about the underlying mechanism of learning in a 1968, 1970; Harter and White, 1968; Ilmberger, reaction time task could be gathered (Pöppel et al, 1986; Jokeit, 1990). Thus, latency distributions of 1990c). Initially response histograms showed a high two response variance without an indication of modes being histograms for choice reaction time show identical separated from each other by some tens of characteristics. Apparently, an underlying decision milliseconds process to initiate a movement shares the same temporal windows. After this initial learning phase, temporal characteristics in spite of the fact that the however, the response histograms became more execution of the movement is implemented in structured, and a clear bimodality developed. In different systems. In all cases – and this is important successive steps of learning the first module for the concept to assume a temporal window - the representing the fastest reaction attracted more same temporal distance of response modes is responses until finally the histogram became observed. The underlying temporal machinery unimodal at a temporal location of the first module. processes of This observation also implies that learning of a approximately 30 to 40 ms; these elementary sensorimotor task might use temporal windows to processing units should not be understood as reach a high level of performance. types of eye information movements in and successive units “physical constants” but as operating ranges with some individual variability. which would indicate discrete And there is further evidence for a temporal window in this operating range: Recordings of What is the reason that quite often one does not single cells show that the visual channel is observe the multimodalities in response histograms characterized by oscillatory responses at an early when choice reaction time is measured, in addition stage of information processing (Podvigin et al., to an inappropriate choice of bin width for the 1992, 2004), indicating that in the afferent pathways registration of responses? Another reason is that before most of the experiments are done under conditions segmentation is taking place that allows the creation of “instationarity”. Usually, subjects have not of temporal windows. Single neurons in the lateral reached a plateau of performance and they are still geniculate nucleus of the cat which receive input in a learning phase for their responses which from the retina, and before they send this increases the variance of responses. To clarify this information to the visual cortex, show stimulus- issue it was tested how long it takes to reach such a triggered oscillations in the same frequency domain. the cortex is reached a temporal 782 心 理 科 学 进 展 第 19 卷 Oscillations with a similar frequency have been approximate speed of 30 ms per item. Another observed also in the somatosensory cortex (Gardner example: In well-trained tasks such as typing or and Costanzo, 1980). These results again support piano playing, up to 30 bits per second are the notion of a general principle of temporally transferred; within approximately 30 ms one-bit segmented information processing as all organisms decisions can be made (Augenstine, 1962), and have to deal with the same challenges. Latour (1967) observed that visual thresholds A rich source of knowledge with respect to this oscillate with a period close to 30 ms. Finally, two temporal window comes also from experiments on experiences that can be distinguished from each sensorimotor synchronization. The task of the other are reported when the overall duration of the subjects in such experiments is to synchronize with two stimuli is 60 ms, i.e., 30 ms for each of the manual responses the regular and sometimes temporally contiguous stimulus events (Efron, irregular sequence of tone stimuli. One usually 1967). Taken together, there is overwhelming observes a small anticipation of the tone by the evidence for the robustness of this time window manual response if the temporal distance of the which serves as a logistical basis for cognitive tones is kept within an operating range of a few processing. seconds. This anticipation of a response itself is often characterized by multimodality (Radil et al., 1990); i.e. the anticipatory movement might occur 4 “Temporal Window” for the Creation of a Subjective Present 30 or 60 ms prior to the stimulus. This observation indicates that the precise execution of an anticipated On a higher level of processing the primordial movement for instance in one second is controlled events as they are made available by the temporal by a temporally segmented process of much higher window discussed above are linked together. frequency; the movement cannot occur at any time Observations made within different experimental but has to select a specific time window to be paradigms provide evidence of the operative executed. Further insight into temporal mechanisms importance of such an integration mechanism and of sensorimotor synchronization comes from a point to a temporal window of just a few seconds systematic experimental (Pöppel, 1997a, 2004, 2009). Although these parameters (Franek et al. 1991a, 1991b; 1994; variation of different observations have been made in different contexts a Mates et al. 1992). One such variation is to common underlying principle is detected in spite of introduce temporal noise in the regular sequence of obvious observational diversities. To look for stimuli which have to be synchronized by manual common principles in different realms of activities responses (Muto et al., 2011). It turns out that a is again guided by the “Darwinian principle” that if temporal variation in the sequence of stimuli a phenomenon shows up in qualitatively different remains unnoticed by the subjects if this variability experiments or situations a general principle has to is kept within the time window to be used for the be suspected. In what follows an answer shall be reduction of temporal uncertainty. given to the question of what the "state of being In most studies as indicated above a value conscious" (Pöppel, 1997b) could mean. The anchor close to 30 ms, or to be more conservative, between point of the reasoning is that one can understand 20 and 60 ms, has been suggested. Additional consciousness only if one analyzes temporal support for this temporal window comes also from mechanisms of neuronal processes and behavioral memory studies. For instance, when using a reaction acts. time paradigm, Sternberg (1975) observed that the The “subjective present” as a basic temporal scanning process which is exhaustive has an phenomenon has interested psychologists for more 第6期 “Temporal Windows” as Logistical Basis for Cognitive Processing 783 than one hundred years (James, 1890; Stern, 1897). to be quite useful in developmental studies (Szelag We are now in a situation to indicate how long such et al., 2002), and also in research with autistic a subjective present may actually last. A numerical children (Szelag et al., 2004). If such children have answer of to reproduce the duration of either visual or auditory experiments or observations which all converge to a stimuli, they show a tendency to reproduce different value of approximately 2 to 3 seconds. Support intervals always close to 2 to 3 seconds. It appears comes can be derived from a number temporal as if they are no longer capable to modulate their perception itself, speech, movement control, vision internal time on the basis of the duration of external and audition, working memory and also the arts stimuli. This experimental task allows a view into (like music or poetry). All these observations the eigen-operations of the brain by indicating suggest that conscious activities are temporally temporal integration as a basic operation of the segmented into intervals of a few seconds and that mental machinery in humans. from different domains like this segmentation is based on an automatic (presemantic) integration process providing a The link of a temporal window to attention has already been suspected in the 19th century temporal platform for conscious activity. It should (Urbantschitsch, 1875), and recent research using be stressed again that the temporal platform does the paradigm of inhibition of return (Zhou, 2008) not have the characteristics of a physical constant has substantiated this close relationship (Bao et al., but that an operating range of approximately 2 to 3 2004, 2011b). A return with full power of attention seconds has been identified; as is typical for to a region in visual space which has been attended biological phenomena, one has to expect some intra- previously is only possible after a few seconds delay. and inter-individual variability. Interestingly, this return takes a little longer for What is the experimental evidence? If subjects more peripheral positions in the visual field which have to reproduce the duration of either an auditory supports the notion of its functional subdivision or a visual stimulus one observes veridical (Bao & Pöppel, 2007; Bao et al., 2010; Bao et al., reproductions with small variance up to 2 to 3 2011a), which has been suggested also for other seconds, and large errors of reproduction with a functions (Frost & Pöppel, 1976; Pöppel et al., 1975, strong tendency for a shorter reproduction with 2011). longer intervals (e.g., Pöppel, 1971). It appears as if Temporal integration can also be studied by short intervals can be experienced as a whole while subjective accentuation of metronome beats. One of longer intervals temporally disintegrate, i.e., during the founding fathers of experimental psychology, short intervals of a few seconds it is possible to Wundt (1911), pointed out that temporal grouping focus the attention continuously onto the stimulus. of successive stimuli has a temporal limit of Possibly, this phenomenon is related to the so called approximately 2.5 seconds. In such a metronome “time-order error” which has been described a long task the subject imposes a subjective structure onto time ago (Köhler, 1923). If one has to compare the identical physical events. If auditory stimuli like intensity of two stimuli, the second one will be click sounds follow each other with an interstimulus judged to be more intense, but apparently only if the interval of for instance one second, it is easy to temporal distance between the comparisons of the impose a subjective structure by giving a subjective two stimuli is too large; for a veridical comparison, accent to every second of the stimuli. If, however, both stimuli have to be presented within a time the temporal interval between the stimuli becomes window of a few seconds only. too long (for instance 5 seconds), one is no longer The value of this rather simple experimental capable to impose such an apparent temporal paradigm of temporal reproduction has been proven structure. The two sequential stimuli no longer can 784 第 19 卷 心 理 科 学 进 展 be united into one percept, i.e. temporal binding for operative range of a time window for 2 to 3 seconds temporally adjacent stimuli is no longer possible (Elbert et al., 1991), and the auditory thalamus can because integration be suspected to be an important structure to be part windows. In experiments with brain injured patients of its implementation as slow oscillations in this it they fall into successive temporal temporal range could be identified (He, 2003). integration process as studied with this metronome Some data in a study by Sams and colleagues (1993) paradigm is selectively impaired after injuries in where the amplitude of the mismatch negativity as a frontal areas of the left hemisphere (Szelag et al., function of the interstimulus interval (ISI) was 1997). Patients with injuries in these areas adopt a investigated also support the above considerations. new strategy of integration by consciously counting The mismatch negativity, a component of the successive events; the "pop-up" impression of auditory event-related potential, is elicited by a belongingness of successive tones is apparently lost physical deviant stimulus such as frequency or in these patients and, thus, they reconstruct intensity of a tone in a homogeneous stimulus togetherness by abstract means. sequence. If during the experiment the ISI is altered, could be demonstrated that the A qualitatively different paradigm providing the largest amplitude of the mismatch negativity is further insight into the integration process comes observed with an ISI of 3 seconds, i.e., shorter and from studies on temporal reversal of ambiguous longer ISIs result in smaller amplitudes of the figures (Gomez et al., 1995; Ilg et al., 2008; Pöppel, mismatch 1997a; Radilova and Pöppel, 1990). If stimuli can increased neuronal activity, this result suggests that be perceived with two perspectives (like the Necker the auditory channel is characterized by a higher cube, or a vase versus two faces looking at each neuronal other) there is an automatic shift of perceptual modulation is endogenously determined, being a content after on average approximately 3 seconds. property of the neuro-cognitive machinery itself, Such a perceptual shift also occurs with ambiguous and it implies that approximately every 3 seconds auditory material, such as the phoneme sequence the sensory channel is more sensitive than at other KU-BA-KU-BA-KU…BA-KU-BA-KU where one times for new information coming from the external hears either KUBA or BAKU; one can subjectively or internal environment. negativity. activity As in negativity regular indicates intervals. This not prevent that after approximately 3 seconds the Temporal integration for intervals of 2 to 3 alternative percept takes possession of conscious seconds is also seen in sensorimotor control. If a content. The spontaneous alteration rate in the two subject is requested to synchronize a regular sensory modalities, i.e., vision and audition, suggest sequence of auditory stimuli with finger taps, that normally after an exhaust period of 2 to 3 stimuli are anticipated with very small variance by seconds attentional mechanisms are elicited that some tens of milliseconds (Mates et al, 1994; open the sensory channels for new information. If Miyake et al., 2001). This kind of sensorimotor the sensory stimulus remains the same, the synchronization is, however, only possible within alternative control. the operating range of a few seconds. If the next Metaphorically speaking, every 2 to 3 seconds, an stimulus lies too far in the future (like 5 seconds) it endogenously generated question arises "what is is new", and with unusual stimuli such as the movement that is precisely linked to stimulus ambiguous material the temporal eigen-operations occurrence; in such a case movements become of the brain are unmasked. irregular and subjects prefer to react to the stimulus interpretation will gain In addition to behavioral studies there is electrophysiological evidence supporting the not possible to program an anticipatory instead of anticipating it. Observations on the duration of intentional 第6期 “Temporal Windows” as Logistical Basis for Cognitive Processing 785 movements coming from ethological studies gave seconds is a general principle of the neuro-cognitive similar numerical values (Schleidt et el., 1987). machinery. This universal integration process is Members of different cultures including those from automatic and presemantic, i.e. it is not determined old ethnia (for instance Yanomami Indians in South by what is processed, but it defines a temporal America) show very similar temporal patterns for window within which conscious activities can be homologous movements, the preferential duration implemented. Because of the omnipresence of this being 2 to 3 seconds. The same time constant could phenomenon, it can be used as a pragmatic be observed when the duration of embraces during definition of the subjective present which is the 2008 olympics in Beijing was measured (Nagy, characterized by the phenomenal impression of 2011); after a victory the winners embraced for "nowness". Temporal integration in the range of 2 to instance their coaches on average three seconds. 3 seconds defines, however, also the singular "state Interestingly, showed of being conscious" or STOBCON (Pöppel, 1997 b). slightly shorter embraces than Asians or Europeans. The 3-second-window provides a logistic basis for On the basis of studies in humans Gerstner and conscious representation, a working platform for Fazio (1995) have observed in various species of our phenomenal present. winners from America higher mammals that they also tend to segment their But may there be another reason that such a motor behavior in the same temporal range as temporal window has been developed in evolution? humans do. This observation suggests that we are One of the greatest challenges for the neuronal dealing with a universal principle of temporal systems is to maintain the identity of a mental integration that transcends human cognition and representation over some time; an additional behavioral control. challenge is to maintain such an identity only for a Supporting evidence for a specific temporal limited time to allow new input to be processed integration mechanism comes also from studies on after some time. Thus, both maintenance of identity memory and speech. In a classical study (Peterson for a mental representation and openness after some and Peterson, 1959) it was shown that the working time platform for short-term retention is just a few requirements for our cognitive machinery. On a seconds; only if rehearsal is allowed are we capable conceptual level it is the complementarity of to maintenance and of dynamics that characterizes store information for longer intervals. for another mental representation are of conscious activity (Pöppel, 2010; Pöppel and Bao spontaneous speech on adults (Vollrath et al., 1992) 2011a, 2011b). This concept of “complementarity as and on children (Kowal et al., 1975) also show that a generative principle” characterizes many domains spoken language is embedded in temporal windows of cognition as in visual processing (Chen, 2005; of up to 3 seconds duration giving speech its Pöppel, 2005), where both bottom-up and top-down rhythmic structure. The importance of a rhythmical mechanisms have to be united to recognize structure in speech and other behavior has already something in its identity. Another example of been stressed some time ago (Martin, 1972). complementarity as a generative principle is given Experiments on the temporal structure As the experimental and other observations in the taxonomy of functions (Pöppel, 1989) which referred to above employ qualitatively different distinguishes between logistical functions (like the paradigms covering perceptual processes in audition “temporal windows”) and content functions (like and vision, cognitive evaluations, movement control, percepts). The representation of content functions is speech, perceptual a necessary condition for conscious activity, but it is accentuation or temporal integration, it is proposed not a sufficient condition; without logistical support that temporal integration in the range of 2 to 3 there would be no consciousness. Thus, the mnemonic representation, 786 第 19 卷 心 理 科 学 进 展 temporal window of a few seconds can be conceived These of as the operative basis both for the maintenance of variations can be used as an experimental paradigm experiments also indicate that diurnal identity and the creation of new identities in to get deeper insight into the functional architecture percepts or other mental contents. of neuro-cognitive systems. Although time estimation shows a diurnal 5 Temporal Processing Applications and some rhythm, this effect is apparently not directly controlled by the circadian oscillator itself. It could be demonstrated (Aschoff, 1985) that there is a Whereas the temporal windows of 20 to 60 significant correlation between the time to be awake milliseconds, and of 2 to 3 seconds represent and the estimation of longer time intervals like mechanisms of self-organization in neuro-cognitive hours, but that there is no such correlation between systems, there is another temporal window which is the estimation of short time intervals and the imposed onto human behavior by the regular cycle duration of wakefulness. These conclusions have of day and night. Research in “chronobiology” has been drawn from experiments when subjects lived shown that the 24-hour rhythm in physiological and for several weeks in complete isolation; under such psychological functions is controlled by an “internal experimental conditions one can observe natural clock” fluctuations of the time being awake allowing the which functions like a self-sustained oscillator (Aschoff, 1965). If subjects live under completely isolated conditions, their internal clock indicated correlative analyses. The importance of the internal clock continues to run, although the “circadian cycle” no controlling the daily behavior of humans can also be longer is exactly 24 hours, but usually a little longer. seen in people who do shift work, or when one has This observation implies that humans have to be to travel to new time zones; it usually takes several synchronized every day with the natural day-night days to be synchronized again with the new time. cycle speeding up the internal clock on average one Interestingly, research on circadian rhythms may hour. also be important for space research. Astronauts, One example of a diurnal rhythm can be seen cosmonauts or taikonauts live in space no longer in time estimation. If subjects have to produce an under the natural conditions of the day night cycle, interval of 10 seconds, they will produce longer and the question arises how their diurnal behavior is intervals in the morning and in the evening, and controlled. In one experiment that served as shorter ones around noon and the early afternoon preparation for space flights (Pöppel, 1968) it could (Pöppel and Giedke, 1970). It has been suspected be shown that social synchronization between that the flow of subjective time might be a potential members of a space crew can be very consequence of the diurnal rhythm of body strong. A group of four male subjects lived for three temperature, but this causal relationship has been weeks under constant conditions in an underground disproven (Pöppel, 1971); (the hypothesis has been bunker. During the first half of the experiment the that as in chemical reactions higher temperature subjects lived synchronized with each other with an results in a speeding up of processes, in this case of average period of 26.2 hours; in the second half of subjective imaging the experiment three subjects lengthened their technology (fMRI) a diurnal variation for particular period to 27.2 hours, and one subject lived areas of the motor system could be described (Peres desynchronized from the group with a period of et al., 2011); and some time ago such a variation has 24.1 hours. This subject also showed some negative been shown for the visual field size in patients who psychological effects possibly due to the different have suffered a postretinal lesion (Zihl et al. 1977). time window he lived in compared to the other time). Using advanced 第6期 “Temporal Windows” as Logistical Basis for Cognitive Processing 787 group members. Such experiments indicate how very selective. In experiments on the effect of important temporal synchronization might be for alcohol on reaction time an interesting dissociation being socially embedded in a group. of function was observed (Pöppel and Steinbach, The importance of temporal windows and 1986). Auditory or visual stimuli were either temporal processing in general has been proven to presented to the left or to the right hemisphere by be of particular importance in medicine. As already presenting stimuli either in the right or left visual mentioned above, a time window in the operating field, or to the right or left ear. Under control range of 30 ms is crucial to understand the effect of conditions it was observed that auditory stimuli anesthesia (Madler and Pöppel, 1987; Schwender el processed in the left hemisphere elicit shorter al., 1994, 1997; Schwilden et al., 2005), and the reaction times compared to stimulation of the right time window of 2 to 3 seconds contributes to a hemisphere; better understanding of autism (Szelag et al., 2004). processed in the right hemisphere elicit shorter As a general rule it can be stated that injuries to the reaction times compared to stimulation of the left brain usually result in a slowing down of processing. hemisphere. Thus, In one patient with a severe injury to the visual selective advantage for processing of auditory cortex several functions showed a significant stimuli in the left and visual stimuli in the right retardation of processing, but this was limited to the hemisphere. Under alcohol this selective advantage visual modality (Pöppel et al., 1978). Simple disappeared, i.e. reaction times to visual or auditory reaction time to visual stimuli became much longer stimuli were the same in either hemisphere. This than those to auditory stimuli. The multimodality in result also implies that there was no or only a the response histograms could still be observed, but minute effect of alcohol for auditory processing in the temporal distance between adjacent modes the right and for visual processing in the left became much longer indicating a central slowing hemisphere. down of visual processing. Of particular interest temporal processing in the two cerebral hemispheres was also the lengthening of visual processing in create experiments on binocular rivalry: Whereas in understanding of neuro-cognitive mechanisms. normal cases the switching of percepts occurs a on the Such unique contrary both visual stimuli hemispheres experimental perspective show a paradigms for a on better Another selective effect of temporal processing patient was observed in patients with brain injuries in approximately half a minute for the alternative view. subcortical regions (Rubia et al., 1997). These Because of this considerable slowing down the patients were required to simply count in steps of patient could describe how the sequential percepts seconds. Under normal circumstances this is no replaced each other; the alternative view moved challenge for anybody. However, these patients gradually across the visual field replacing smoothly showed an unusual pattern of counting: some of the old view. This observation is of general them counted twice as fast as normal, others importance as it suggests that percepts are not counted half as fast. A very small injury in constructed at the same time in distributed areas, subcortical but that they are constructed in a sequential way strategically important structures which normally which, however, normally remains unnoticed. Such have to interact to allow counting in seconds as one a slowing down of visual processing after brain has learned it. The selection of either double or half injury has also been observed when patients had to the speed of normal counting indicates that two read (Pöppel and Shattuck, 1974; Woods and Pöppel, oscillatory processes of high and of low frequency 1974). provide a logistic frame for interaction to create a within a few seconds, it took the However, a central slowing down can also be areas apparently disconnected stable temporal process between these frequencies. 788 第 19 卷 心 理 科 学 进 展 An understanding of temporal processing is motives in western music like Johann Sebastian also important for the restitution of functions in Bach, Ludwig van Beethoven or Richard Wagner, patients who have suffered a brain injury (von one often observes that the duration of these Steinbüchel and Pöppel, 1993). In a taxonomy of musical expressions uses the time window of 2 to 3 functions which is based on neuropsychological seconds; if a motif is played too slow or too fast, observations (Pöppel, 1989; Pöppel and Ruhnau, immediately the aesthetic value is compromised. 2011) it has been stressed that it is necessary to Recent experimental evidence suggests a close link distinguish functions between temporal patterns and movements of the (“How-functions”) like temporal processing and body (Su and Pöppel, 2011) stressing how important content functions (“What-functions”). If patients the human body is for the experience of music. between logistical have suffered for instance an injury affecting their Finally, a completely different field of competence in speech (e.g., Szelag et al., 1997) it is application is the use of temporal processing as a not sufficient to concentrate in the therapeutic research paradigm, i.e. using temporal processing as process only on aspects of linguistic competence an experimental window to better understand like the lexical, syntactic or semantic competence, neuro-cognitive mechanisms. One such paradigm is but one has also to take into account basic for instance provided by using voluntarily delayed mechanisms of temporal processing. A slowing responses with feedback (Szelag et al., 2001). If a down of central mechanisms in the auditory system subject does not have to react as fast as possible to a can make it impossible for a patient to understand stimulus, but has to delay the response by a speech as it is normally spoken (Albert and Bear, pre-defined interval, one observes a unique response 1974). Only if the logistical basis of temporal pattern íf one analyzes the variance of reactions. For processing is also appreciated will it be possible to delayed responses up to approximately half a obtain satisfactory rehabilitation of function. second the variance is very high, but for longer A completely different domain where temporal delayed responses the variance is significantly processing has been shown to be important is the smaller although this phenomenon may appear arts, i.e., poetry and music. If one analyzes the contra-intuitive. This observation implies that temporal structure of poems in different languages, conscious control on the passage of time sets in only one observes that the duration of a verse is usually after approximately half a second, in spite of the embedded within the time window of 2 to 3 seconds fact that it is possible to react much faster. 1994). Using temporal indicators for a deeper insight Irrespective of the syntactic rules, word length or into neuro-cognitive processing has in particular semantic preferences in different languages, poets at been harvested successfully by Zhou and colleagues. all times apparently have had an implicit knowledge It could for instance be shown using temporal (Pöppel structure processing as an indicator that the human visual temporally a poem, be it Sappho in old Greece more field is subdivided into different functional domains than 2500 years ago, be it Li Bai during the Tang (Zhou et al, 2010a) verifying previous observations. Dynasty in China some 1300 years ago, be it In other experiments it could be demonstrated how Shakespeare some 400 years ago, or poets of our conscious time. The human brain imposes a temporal window temporal experience (Zhou et al., 2010b). And of 2 to 3 seconds which is used for an optimal finally, in another experimental paradigm it could aesthetic representation. Interestingly, this temporal be demonstrated that temporal perception can be window also dominates musical expression (Pöppel, used as an indicator to get a better understanding of 1988). If one measures the duration of musical visual feature (e.g. orientation) processing in the (Turner and and Pöppel, Bao, 1988; 2011a) Pöppel, how to and subconscious processing affect 第6期 “Temporal Windows” as Logistical Basis for Cognitive Processing visual cortex (Zhou and Han, 2011). Thus, temporal windows and temporal processing in general prove to be important for deeper insights into cognitive processing. Donders, K. (1868 / 1969). On the speed of mental processes. Acta Psychologica, 30, 412−431. Efron, R. (1967). The duration of the present. Annals of the New York Academy of Sciences, 138, 713−729. Elbert, T., Ulrich, R., Rockstroh, B., & Lutzenberger, W. Refferences Albert, M. L., & Bear, D. (1974). Time to understand – a case study of word deafness with reference to the role of time in auditory comprehension. Brain, 97, 373−384. (1991). The processing of temporal intervals reflected by CNV-like brain potentials. Psychophysiology, 28, 648−655. Fang, Y., & Bao, Y. (2011). Independence of tone order Aschoff, J. (1965). Circadian rhythms in man. Science, 148, 1427−1432. threshold from tone frequency. To be submitted to Acta Neurobiologiae Experimentalis. Aschoff, J. (1985). On the perception of time during prolonged temporal isolation. Human Neurobiology, 4, 41−52. Fechner, G. T. (1860). Elemente der Psychophysik. Leipzig, Breitkopf und Härtel. Fink, M., Ulbrich, P., Churan, J., & Wittmann, M. (2006). Stimulus-dependent Augenstine, L.G. (1962). A model of how humans process information. Biometrics. 18, 420−421. mechanisms underlying of the return. processing of temporal order. Behavioural Processes, 71, 344−352. Franek, M., Mates, J., Radil, T., Beck, K., & Pöppel, E. Bao, Y., Li, H., Liu, J., & Pöppel, E. (2010). Neural inhibition 789 eccentricity International effect Journal of of Psychophysiology, 77, 296. (1991a). Finger tapping in musicians and nonmusicians. International Journal of Psychophysiology, 11, 277−279. Franek, M., Mates, J., Radil, T., Beck, K., & Pöppel, E. (1991b). Sensorimotor synchronization: Motor responses to regular auditory patterns. Perception & Psychophysics, Bao, Y., & Pöppel, E. (2007). Two spatially separated attention systems in the visual field: evidence from 49, 509−516. Franek, M., Mates, J., Radil, T., Beck, K., & Pöppel, E. (1994). Sensorimotor synchronization: Motor responses to inhibition of return. Cognitive Processing, 8, 37−44. Bao, Y., Sander, T., Trahms, L., Pöppel, E., Lei, Q., & Zhou, B. (2011a). The eccentricity effect of inhibition of return is resistant to practice. Submitted to Neuroscience Letters. Bao, Y., Wang, Y., Pöppel, E., & Li, H. (2011b). Different temporal dynamics of inhibition of return in the visual field. Submitted to Naturwissenschaften. pseudoregular auditory patterns. Perception Frost, D., & Pöppel, E. (1976). Different programming modes of human saccadic eye movements as a function of stimulus eccentricity: subdivision of the Indications human visual of a functional field. Biological Cybernetics, 23, 39−48. Galambos, R., Makeig, S., & Talmachoff, P. J. (1981). A Bao, Y., Zhou, J., & Fu, L. (2004). Aging and the time course 40-Hz auditory potential recorded from the human scalp. of inhibition of return in a static environment. Acta Proceedings National Academy Sciences, USA, Neurobiologiae Experimentalis, 64, 403−414. 2643−2647. Bao, Y., Szymaszek, A., Wang, X., Fang, Y., Oron, A., & Szelag, E. (2011c). Linguistic experience alters auditory perception of temporal order: a comparison between tonal and non-tonal language users. Submitted to Journal of Experimental Psychology: Human Perception and Performance. Chen, L. (2005). The topological approach to perceptual organization. Visual Cognition, 12, 553−637. Darwin, C. (1859). The origin of species. London, John Murray. & Psychophysics, 55, 204−217. 78, Gardner, E. P., & Costanzo, R. M. (1980). Temporal integration of multiple-point stimuli in primary somatosensory cortical receptive fields in alert monkeys. Journal of Neurophysiology, 43, 444−468. Gerstner, G. E., & Fazio, V. A. (1995). Evidence for a universal perceptual unit in mammals. Ethology, 101, 89−100. Gomez, C., Argandona, E. D., Solier, R. G., Angulo, J. C., & Vazquez, M. (1995). Timing and competition in networks representing ambiguous figures. Brain & Cognition, 29, 103−114. Gutyrchik, E., Churan, J., Meindl, T., Bokde, A. L., von 790 第 19 卷 心 理 科 学 进 展 Bernewitz, H., Born, C., Reiser, M., Pöppel, E., & Szelag, E. (2008). Towards electrophysiological correlates Wittmann, of auditory perception of temporal order. Neuroscience M. (2010). Functional neuroimaging of duration discrimination on two different time scales. Neuroscience Letters, 469, 411−415. Hari, R., & Kiesilä, P. (1996). Deficit of temporal auditory processing in dyslexic adults. Neuroscience Letters, 205, 138−140. Roenneberg, T. (1999). Daily rhythm of temporal resolution in the auditory system. Cortex, 35, 89−100. Mach, E. (1865). Untersuchungen über den Zeitsinn des Harter, M.R., & White, C. T. (1968). Periodicity within reaction Letters, 437, 139−143. Lotze, M., Wittmann, M., von Steinbüchel, N., Pöppel, E., & time distributions and electromyograms. Quarterly Journal of Experimental Psychology, 20, 157−166. Ohres. Sitzungsberichte naturwissenschaftlichen der Classe mathematischder Kaiserlichen Akademie der Wissenschaften 51, II.Abteilung, 133−150. Madler, C., & Pöppel, E. (1987). Auditory evoked potentials He, J. (2003). Slow oscillation in non-lemniscal auditory thalamus. Journal of Neuroscience, 23, 8281−8290. indicate the loss of neuronal oscillations during general anaesthesia. Naturwissenschaften, 74, 42−43. Helson, H. (1964). Adaptation-level theory. New York, Harper and Row. Martin, J.G. (1972). Rhythmic (hierarchical) versus serial structure in speech and other behavior. Psychological Hirsh, I.J., & Sherrick, C. E. (1961). Perceived order in different sense modalities. Journal of Experimental Psychology, 62, 423−432. Review, 79, 487−509. Mates, J., Müller, U., Radil, T., & Pöppel, E. (1994). Temporal integration in sensorimotor synchronization. Ilg, R., Burazanis, S., Wohlschläger, A. M., Wöller, A., Wagenpfeil, S., & Mühlau, M. (2008). Stimulus frequency Journal of Cognitive Neuroscience, 6, 332−340. Mates, J., Radil, T., & Pöppel, E. (1992). Cooperative influences spontaneous perceptual reversals in ambiguous tapping: Time control under different feedback conditions. apparent Perception & Psychophysics, 52, 691−704. motion. Perception & Psychophysics, 70, 437−442. Miyake, Y., Onishi, Y., & Pöppel, E. (2004). Two types of Ilg, R., Vogeley, K., Goschke, T., Bolte, A., Shah, J., Pöppel, E., & Fink, G. (2007). Neuronal processes underlying intuitive coherence judgments as revealed by fMRI on a semantic judgment task. NeuroImage, 38, 228−238. Ilmberger, J. (1986). Auditory excitability cycles in choice reaction time and order threshold. Naturwissenschaften, 73, 743−744. Henry Holt. synchronization tapping. Acta Muto Y., Miyake, Y., & Pöppel, E. (2011) Temporal tolerance in sensorimotor synchronization. To be submitted to Neuroscience Letters. Nagy, E. (2011). Sharing the moment: the duration of January 2011) Nauta, Jokeit, H. (1990). Analysis of periodicities in human reaction times. Naturwissenschaften, 77, 298−291. Temporal order judgement for auditory and visual stimuli. Acta Neurobiologiae Experimentalis, 62, 263−270. Köhler, W. (1923). Zur Theorie des Sukzessivvergleichs und der Zeitfehler. Psychologische Forschung, 4, 115−175. Kolodziejczyk, I., & Szelag, E. (2008). Auditory perception of temporal order in centenarians in comparison with elderly subjects. Acta W.J.H., Neurobiologiae Experimentalis, 68, 373−381. Kowal, S., O'Connell, D. C., & Sabin, E. J. (1975). & Feirtag, M. (1986). Fundamental neuroanatomy. New York, NY, Freeman and Co. Newton, Kanabus, M., Szelag, E., Rojak, E., & Pöppel, E. (2002). and in embraces in humans. Journal of Ethology (publ. Online 18 James, W. (1890). The principles of psychology. New York, young anticipation Neurobiologiae Experimentalis, 64, 415−426. I. (1687). Philosophiae Naturalis Principia Mathematica. Trans. and Ed. Cajori, F. 1934, University of California Press. Peres, I., Vetter, C., Blautzik, J., Reiser, M., Pöppel, E., Meindl, T., Roenneberg, T., & Gutyrchik, E. (2011). Neural Activation of the Motor System Shows Region-specific Time-of-Day Differences. NeuroImage, in press. Peterson, L.B., & Peterson, M. J. (1959). Short-term retention of individual items. Journal of Experimental Psychology, 58, 193−198. Development of temporal patterning and vocal hesitations Podvigin, N. F., Bagaeva, T. V., Boykova, E. V., Zargarov, A. in spontaneous narratives. Journal of Psycholinguistic A., Podvigina, D. N., & Pöppel, E. (2004). Three bands of Research, 4, 195−207. oscillatory activity in the lateral geniculate nucleus of the Latour, P.L. (1967). Evidence of internal clocks in the human operator. Acta Psychologica, 27, 341−348. Lewandowska, M., Bekisz, A., Szymaszek, A., Wrobel, A., & cat visual system. Neuroscience Letters, 361, 83−85. Podvigin, N.F., Jokeit, H., Pöppel, E., Chizh, A., & Kiselyeva, N. (1992). Stimulus dependent oscillatory 第6期 “Temporal Windows” as Logistical Basis for Cognitive Processing activity in the lateral geniculate body of the cat. E. (1968). Desynchronisationen circadianer Rhythmen innerhalb einer isolierten Gruppe. Pflügers Archive, 299, 364−370. Pöppel, E. (1968). Pöppel, E., Brinkmann, R., von Cramon, D., & Singer, W. (1978). Association and dissociation of visual functions in Naturwissenschaften, 79, 428−431. Pöppel, 791 a case of bilateral occipital lobe infarction. Archiv für Psychiatrie und Nervenkrankheiten, 225, 1−21. Pöppel, E., von Cramon, D., & Backmund, H. (1975). Oszillatorische Komponenten in Reaktionszeiten. Naturwissenschaften, 55, 449−450. Eccentricity-specific dissociation of visual functions in patients with lesions of the central visual pathways. Pöppel, E. (1970). Excitability cycles in central intermittency. Psychologische Forschung, 34, 1−9. Nature, 256, 489−490. Pöppel E., & Giedke, H. (1970). Diurnal variation of time Pöppel, E. (1971). Oscillations as possible basis for time perception. Studium Generale, 24, 85−107. perception. Psychologische Forschung, 34, 182−198. Pöppel, E., & Logothetis, N. (1986). Neuronal oscillations in Pöppel, E. (1978) Time perception. In: R. Held, H.W. the human brain. Discontinuous initiations of pursuit eye Leibowitz, H.-L. Teuber (Eds.), Handbook of Sensory movements indicate a 30-Hz temporal framework for Physiology, Vol. VIII: Perception. Berlin: Springer, visual information processing. Naturwissenschaften, 73, 713−729. 267−268. Pöppel, E. (1988). The measurement of music and the cerebral clock: A new theory. Leonardo, 22, 83−89. Modelle angewiesene Angelegenheit ohne Taxonomie- Pöppel, E. (1989). Taxonomy of the subjective: An evolutionary perspective. In: J.W. Pöppel, E., & Ruhnau, E. (2011). Psychologie als eine auf Brown eine Polemik. Leopoldina Jahresbericht, in press. (Ed.) Pöppel, E., Ruhnau, E., Schill, K., von Steinbüchel, N. Neuropsychology of Visual Perception (pp.219−232). (1990a). A hypothesis concerning timing in the brain. In: Lawrence Erlbaum Associates, Hillsdale, New Jersey. Pöppel, E. (1994). Temporal mechanisms in perception. International Review of Neurobiology, 37, 185−202. Verlag Berlin/Heidelberg. Pöppel, E. (1997a) A hierarchical model of temporal perception. Trends in Cognitive Sciences, 1, 56−61. conscious. Behavioral and Brain Sciences 20, 155−156. Pöppel, E. (2004). Lost in time: a historical frame, elementary processing units and the 3-second window. Acta Neurobiologiae Experimentalis, 64, 295−301. in visual perception. Visual Cognition, 12, 665−670. cognitive processing. Multistable states in intrahemispheric learning of a sensorimotor task. NeuroReport, 1, 69−72. with brain wounds involving the central visual pathways. Cortex, 10, 84−88. (2009). Pre-semantically defined temporal for states: A hypothesis. Naturwissenschaften, 77, 89−91. Pöppel, E., Schill, K., & von Steinbüchel, N. (1990c). Pöppel, E., & Shattuck, S. R. (1974). Reading in patients Pöppel, E. (2005). Complementarity as a generative principle windows Pöppel, E., Schill, K., & von Steinbüchel, N. (1990b). Sensory integration within temporally neutral system Pöppel, E. (1997b). Consciousness versus states of being Pöppel, E. H. Haken, M. Stadler (Eds.): Synergetics of Cognition (pp.144−149). Springer Series in Synergetics 45. Springer Philosophical Transactions of the Royal Society B, 363, 1887−1896. Pöppel, E., & Steinbach, T. (1986). Selective vulnerability of the two cerebral hemispheres under alcohol. Naturwissenschaften, 73, 327−328. Pöppel, E. (2010). Perceptual identity and personal self: Pöppel, E., Bao, Y., & Zhou, B. (2011). Beyond blindsight: Neurobiological reflections: In: Tomasz Maruszewski, Seeing moving stimuli within an area of blindness. To be Malgorzata Fajkowska Michael M. Eysenck, (Eds): “Personality submitted to Nature Neuroscience. social Radil, T., Mates, J., Ilmberger, J. Pöppel, E. (1990). Stimulus Publications, anticipation in following rhythmic acoustical patterns by Pöppel, E., & Bao, Y. (2011a). Three modes of knowledge as Radilová, J., & Pöppel, E. (1990). The perception of figure basis for intercultural cognition and communication: A reversal as a function of contrast reversal exemplified with the theoretical perspective In: Shihui Han, Ernst Pöppel (eds): Schröder staircase. Acta Neurobiologiae Experimentalis, 50, from biological, perspectives”(pp.75−82). Eliot cognitive, Werner and Clinton Corners, New York. Culture and Neural Frames of Cognition and Communication (pp.215−231). Springer-Verlag, Heidelberg. Pöppel, E., & Bao, Y. (2011b). Subjective Time: temporal windows as bridge to objective time. In: Dan Lloyd and Valtteri Arstila (Eds.), Subjective Time, MIT Press, in press. tapping. Experientia, 46, 762−763. 37−40. Rubia, K., Schuri, U., von Cramon, D. Y., & Pöppel, E. (1997). Time estimation as a neuronal network property: a lesion study. Neuroreport, 8, 1273−1276. Ruhnau, E. (1994). The now - the missing link between matter and mind. In: M. Bitbol, E. Ruhnau (eds). Now, 792 Time and Quantum Mechanics (pp.101−130). Gif-sur-Yvette, Editions Frontieres. in quantum International Journal physics of and brain Theoretical physiology. Physics, 30, 1083−1090. Temporal processing disorders in patients with Broca's aphasia. Neuroscience Letters, 235, 33−36. Szymaszek, A., Sereda, M., Pöppel, E., & Szelag, E. (2009). Individual differences in the perception of temporal order: Sams, M., Hari, R., Rif, J., & Knuutila, J. (1993). The human auditory sensory memory trace persists about 10 sec: Neuromagnetic evidence. Journal of Cognitive Neuroscience, 5, 363−370. universal constant in temporal segmentation of human short-term behaviour. Naturwissenschaften, 74, 289−290. and effect of age and cognition. Cognitive Neuropsychology, 26, 135−147. Szymaszek, A., Szelag, E., & Sliwowska, M. (2006) suppression of effect of age, gender, listener practice and stimulus presentation mode. Neuroscience Letters, 403, 190−194. Turner, F., & Pöppel, E. (1988). Metered poetry, the brain, Schwender, D., Daunderer, M., & Pöppel, E. (1997). Central effects the Auditory perception of temporal order in humans: The Schleidt, M., Eibl-Eibesfeldt, I., & Pöppel, E. (1987). A anaesthetic Experimentalis, 61, 175−179. Szelag, E., von Steinbüchel, N., & Pöppel, E. (1997). Ruhnau, E., & Pöppel, E. (1991). Adirectional temporal zones 第 19 卷 心 理 科 学 进 展 auditory information processing during general anaesthesia. Theory of Biosciences, 116, 284−289. and time, in: I. Rentschler, B. Herzberger, D. Epstein (eds.): Beauty and the Brain. Biological Aspects of Aesthetics (pp.71−90). Birkhäuser, Basel. Urbantschitsch, V. (1875). Über eine Eigenthümlichkeit der Schwender, D., C. Madler, S. Klasing, K. Peter & E. Pöppel. (1994): Anesthetic control of 40-Hz brain activity and Schallempfindungen geringster Intensität. Centralblatt für die medizinischen Wissenschaften, 13, 625−628. 3, Vierordt, K. (1868). Der Zeitsinn nach Versuchen. Tübingen: Schwilden, H., Kochs, E., Daunderer, M., Jeleazcov, C., Vollrath, M., Kazenwadel, J., & Krüger, H. P. (1992). A Scheller, B., Schneider, G., Schüttler, J., Schwender, D., universal constant in temporal segmentation of human implicit memory. Consciousness and Cognition, 129−147. Laupp. Stockmanns, G., & Pöppel, E. (2005). Concurrent speech. Naturwissenschaften, 79, 479−480. recording of AEP, SSEP and EEG parameters during von Baer, K. E. (1864). Welche Auffassung der lebenden Natur anaesthesia – a factor analysis. British Journal of ist die richtige? Und wie ist diese Auffassung auf die Anaesthesia, 95, 197−206. Entomologie anzuwenden? In H. Schmitzdorff (ed.), Reden Steinbach, T., von Dreden G., & Pöppel, E. (1991). gehalten in wissenschaftlichen Versammlungen und kleinere Long-term training in a choice reaction time task reveals Aufsa¨tze vermischten Inhalts (pp. 237–284). St Petersburg, different learning characteristics for the visual and auditory system. Naturwissenschaften, 78, 185−187. Stern, L.W. (1897). Psychische Präsenzzeit. Zeitschrift für Psychologie und Physiologie der Sinnesorgane, 13, 325−349. Russia: Verlag der kaiserlichen Hofbuchhandlung. von Steinbüchel, N., & Pöppel, E. (1993). Domains of rehabilitation: a theoretical perspective. Behavioural Brain Research, 56, 1−10. Wada, M., Moizumi, S., & Kitazawa, S. (2005). Temporal Sternberg, S. (1975). Memory scanning: new findings and current controversies. Quarterly Journal of Experimental Psychology, 27, 1−32. order judgment in mice. Behavioral Brain Research, 157, 167−175. Wiener, N. (1958). Time and the science of organization. Su, Y. H., & Pöppel, E. (2011). Body movement enhances the extraction of temporal structures in auditory sequences. Psychological Research in press. Scientia, 93, 199−205. Wittmann, M., Burtscher, A., Fries, W., & von Steinbüchel, N. (2004). Effects of brain lesion size and location on Szelag, E., Kowalska, J., Rymarczyk, K., & Pöppel, E. (2002). Duration processing in children as determind by temporal-order judgment. NeuroReport 15, 2401−2405. Woods B. T., Pöppel, E. (1974). Effect of print size on time reproduction: implications for a few seconds reading temporal window. Acta Psychological, 110, 1−9. Neuropsychologia, 12, 31−41. Szelag, E., Kowalska, J., Galkowski, T., & Pöppel, E. (2004). Temporal processing deficits in high-functioning children with autism. British Journal of Psychology, 95, 269−282. Szelag, E., Rymarczyk, K., & Pöppel, E. (2001). Conscious control of movements: increase of temporal precision in voluntarily delayed actions. Acta Neurobiologiae time in a patient with a verbal alexia. Wundt, W. (1911). Einführung in die Psychologie. Leipzig: Voigtländer. Zhou, B. (2008). Disentangling perceptual and motor components in inhibition of return. Cognitive Processing, 9, 175−187. Zhou, B., Bao, Y., Sander, T., Trahms, L, & Pöppel, E. 第6期 “Temporal Windows” as Logistical Basis for Cognitive Processing 793 (2010a). Dissociation of summation and peak latencies in Zhou, B., Yang, S., Mao, L., & Han, S. (2011). Contributions visual processing: An MEG study on stimulus eccentricity. of early visual cortex to conscious temporal perception. To Neuroscience Letters, 483, 101−104. be submitted to Current Biology. Zhou, B., Qin, J., Mao, L., Han, S., & Pöppel, E. (2010b). Zihl, J., Pöppel, E., & von Cramon, D. (1977). Diurnal Modulations of temporal perception by consciously and variation of visual field size in patients with postretinal unconsciously perceived stimuli. Perception, 39, 900−908. lesions. Experimental Brain Research, 27, 245−249. “时间窗”—— 认知加工的后勤基础 Ernst Pöppel1,2; 包 燕 1,2; 周 斌 1,3 (1 德国慕尼黑大学医学心理研究所及人类科学中心) ( 北京大学心理学系及机器感知与智能教育部重点实验室, 北京 100871) (3 中国科学院心理研究所, 北京 100101) 2 摘 要 时间加工是认知加工的内在属性。因此, 理解发生在知觉或更广泛的认知过程中的时间加工极为重 要。为了应对中枢信息加工所面临的外部挑战, 大脑显然已形成了一些用于整合信息的特殊时间窗。已经发 现, 其中一个时间窗介于数十毫秒的范围内, 它用于为意识活动产生必要的建构单元。来自反应时、时序阈限 以及神经元结构振荡反应的研究为该时间窗的存在提供了实证证据。另一个时间窗的作用范围是 2~3 秒, 它 用于产生“主观现在感”或作为使知觉体的标识保持不变的时间整合区间。支持该窗口存在的实验证据来自时 距再现、两可图形、感觉运动同步以及神经生理学研究。还有一种时间窗以昼夜节律的形式存在。所有的心 理和生理功能似乎都有着 24 小时的周期性变化。时间窗的紊乱会以神经或精神疾病的形式表现出来, 这恰恰 表明了在基础研究之外对时间加工进行研究的重要性。 关键词 时间知觉; 顺序阈限; 反应时; 神经元振荡; 昼夜节律 分类号 B842
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